[go: up one dir, main page]

TWI288479B - Bipolar transistor with graded base layer - Google Patents

Bipolar transistor with graded base layer Download PDF

Info

Publication number
TWI288479B
TWI288479B TW92107363A TW92107363A TWI288479B TW I288479 B TWI288479 B TW I288479B TW 92107363 A TW92107363 A TW 92107363A TW 92107363 A TW92107363 A TW 92107363A TW I288479 B TWI288479 B TW I288479B
Authority
TW
Taiwan
Prior art keywords
layer
base
collector
emitter
band gap
Prior art date
Application number
TW92107363A
Other languages
Chinese (zh)
Other versions
TW200308088A (en
Inventor
Roger E Welser
Paul M Deluca
Charles R Lutz
Kevin S Stevens
Original Assignee
Kopin Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from US10/121,444 external-priority patent/US6847060B2/en
Application filed by Kopin Corp filed Critical Kopin Corp
Publication of TW200308088A publication Critical patent/TW200308088A/en
Application granted granted Critical
Publication of TWI288479B publication Critical patent/TWI288479B/en

Links

Landscapes

  • Bipolar Transistors (AREA)

Abstract

A semiconductor material which has a high carbon dopant concentration includes gallium, indium, arsenic and nitrogen. The disclosed semiconductor materials have a low sheet resistivity because of the high carbon dopant concentrations obtained. The material can be the base layer of gallium arsenide-based heterojunction bipolar transistors and can be lattice-matched to gallium arsenide emitter and/or collector layers by controlling concentrations of indium and nitrogen in the base layer. The base layer can have a graded band gap that is formed by changing the flow rates during deposition of III and V additive elements employed to reduce band gap relative to different III-V elements that represent the bulk of the layer. The flow rates of the III and V additive elements maintain an essentially constant doping-mobility product value during deposition and can be regulated to obtain pre-selected base-emitter voltages at junctions within a resulting transistor.

Description

1288479 玖、發明說明: 【發明所屬之技術領域】 本發明係關於電晶體,尤其係關於具分級基極層的雙 極電晶體。 【先前技術】 雙極接合電晶體(bipolar junction transistor,BJT) 和異質接合雙極電晶體(heterojunction bipolar transistor,HBT)的積體電路(integrated circuit,1C)已 經發展成為多種應用的重要科技,尤其是做為無線手機、 微波儀器以及光纖通訊系統之高速電路(每秒大於一百億 位元)的功率放大器。預期未來的需求乃需要具有較低操 作電壓、較高頻率的表現、較高附加功率的效率以及較低 製造成本的元件。BJT或HBT的打開電壓(Vbe〇n)#定義成 達到一定之固定集極電流密度(jc)所需要的基極一射極電 壓(Vbe)。對於供應電壓受限於電池科技和其他組件之功率 需求的低功率應用而言,此打開電壓可以限制元件的可用 性0 ,不像BJT中的射極、基極和集極係由一種半導體材料 所製成,HBT係' 由兩種不相似的半導體材料所製成,宜中 射極半導體材料的能帶間隙_、e 要 做成基極之半導體材料的 P)要比 到集極的載子注入效率優 等致從基極 子注入從基極回到射極的 、登 戰 F早一擇具有較小能帶間隙的 1288479 基極可降低打開電,此乃因為從基極到集極之載子注入 =率的增加會在給定的基極—射極㈣下增加集極的電流 禮、度。 然而,HBT的半導體材料於異質接合處之能帶對齊且 有突然不連續的缺點’此可導致纟膽的射極—基極界面 處有傳導能帶的突峰(spike)。此傳導能帶突♦的效應是阻 礙了電子從基極出來傳輸到集極。因&,電子待在基極比 較久’導致再結合的程度增加以及集極電流增益(心的 減少。如上所討論的,由於異質接合雙極電晶體的打開電 麼乃定義成達到-定之固定集極電流密度所需要的基極— 射極電壓’所以降低集極電流增益有效地提昇耐的打開 電愚。因此’ HBT半導體材料的製造需要進一步改良,以 降低打開電壓,藉此改善低電壓操作的元件。 【發明内容】 本發明提供一種HBT,其具有n型捧雜的集極、形成 於集極上而由ΠΙ-ν族材料(包括麵和氮)所組成的基極、 以及形成於基極上之η型摻雜的射極。基極層的m_v族 材料具有大約^χΠ)%-3到大約7〇xl〇19cra_3的碳摻雜濃 度。在-較佳的具體態樣中,基極層包括鎵、銦、碎和氮 元素。相對於GaAs的能帶間隙而言,銦和氮的存在減少了 此材料的能帶間隙。此外’此材料中的推雜濃度為高,而 片電阻(Rsb)為低。相對於具有類似摻雜濃度之基極 層的’而言,這些因素導致較低的打開電塵。 1288479 在一較佳的具體態樣中 T 11 J—V族化合物材料系統可 以由化學式GahlrixAs〗N夾冲志 α . 术代表。已知當少量的氮併入 Gai_xInxAs時,此材料的能帶間隙會實質地降下來。再者 ’因為氮以相反於鋼的方向來推叙曰 U ^推勳晶袼常數,所以把銦對 氮的適當比例加入此材料,可以長出晶格匹配力—的1288479 发明, DESCRIPTION OF THE INVENTION: TECHNICAL FIELD OF THE INVENTION The present invention relates to transistors, and more particularly to bipolar transistors having a graded base layer. [Prior Art] A bipolar junction transistor (BJT) and a heterojunction bipolar transistor (HBT) integrated circuit (1C) have been developed into important technologies for various applications, especially It is a power amplifier for high-speed circuits (greater than 10 billion bits per second) for wireless handsets, microwave instruments, and fiber-optic communication systems. Future demand is expected to require components with lower operating voltage, higher frequency performance, higher added power efficiency, and lower manufacturing cost. The turn-on voltage (Vbe〇n)# of the BJT or HBT is defined as the base-emitter voltage (Vbe) required to achieve a certain fixed collector current density (jc). For low power applications where the supply voltage is limited by the power requirements of battery technology and other components, this turn-on voltage can limit the usability of the component 0, unlike the emitter, base, and collector of BJT, which is made of a semiconductor material. Made, the HBT system is made of two dissimilar semiconductor materials. The band gap of the emitter semiconductor material should be _, the P of the semiconductor material to be the base is compared to the collector of the collector. The injection efficiency is excellent from the base-subjection from the base back to the emitter, and the 1288479 base with a small energy gap can reduce the turn-on power because of the carrier from the base to the collector. An increase in the injection rate will increase the current of the collector at a given base-emitter (four). However, the ability of the HBT semiconductor material to be aligned at the heterojunction and has a sudden discontinuity' can result in a spike in the conduction band at the emitter-base interface of the bladder. The effect of this conduction band is that the electrons are transmitted from the base to the collector. Because &, the electron stays at the base for a long time' leads to an increase in the degree of recombination and a collector current gain (reduction of the heart. As discussed above, since the open junction bipolar transistor is turned on, it is defined as The base-emitter voltage required to fix the collector current density' therefore reduces the collector current gain and effectively increases the resistance to open the circuit. Therefore, the manufacture of HBT semiconductor materials needs to be further improved to reduce the turn-on voltage, thereby improving the low Voltage-operated component. SUMMARY OF THE INVENTION The present invention provides an HBT having a collector of n-type dopants, a base formed on a collector and composed of a ΠΙ-ν family material (including a face and nitrogen), and a formation The n-type doped emitter on the base. The m_v material of the base layer has a carbon doping concentration of about χΠ)%-3 to about 7〇xl〇19cra_3. In a preferred embodiment, the base layer comprises gallium, indium, minced and nitrogen elements. The presence of indium and nitrogen reduces the band gap of the material relative to the band gap of GaAs. In addition, the dopant concentration in this material is high and the sheet resistance (Rsb) is low. These factors result in a lower open electrical dust relative to the 'base layer with similar doping concentration'. 1288479 In a preferred embodiment, the T 11 J-V compound material system can be represented by the chemical formula Gahlrix As. It is known that when a small amount of nitrogen is incorporated into Gai_xInxAs, the band gap of this material will substantially fall. Furthermore, because nitrogen deduces the 曰 U ^ push crystallization constant in the opposite direction to the steel, the appropriate ratio of indium to nitrogen is added to the material to grow the lattice matching force.

Gai_xInxAs卜A合金。因此可以消除導致能量間隙增加和材 料差排不配的多餘應變。因此撰接/ U ^送擇此降低或消除應變之銦 對氮的比例。在本發明的糙祛且辨能描+ — J平乂住具體態樣中,ίίΒΤ之基極層Gai_xInxAs A alloy. Therefore, it is possible to eliminate excess strain that causes an increase in the energy gap and a mismatch in the material. Therefore, the splicing / U ^ is chosen to reduce or eliminate the strain of indium to nitrogen ratio. In the roughening of the present invention and the identification of the J-level, the base layer of the ίίΒΤ

GabxIrixASi-yNy 中的 x=3y。 在具有GaAs的傳統HBT中,隨著溫度的增加’以致電 洞注入射極程度較高,$間電荷層的再結合電流較高,並 且基極中的擴散長度可能較短,故電流增益典型上會降低 。在具有GalnAsN基極層的HBT巾,隨著溫度的增二,發 現電流增益有顯著的增加(每rc大約升高〇3%)。此結果 乃解釋為擴散長度隨著溫度的增加而有所增加。如果^帶 底部的電子乃侷限於它們是至少料地局部化的狀態;苹 則預期會有此種效應,並且隨著溫度的增加,它們從上述 狀態熱激發到電子可以更輕易擴散的其他狀態。因此,以 GalnAsN設計構成基極層則改進了本發明HBT的溫度特徵 ,並且減少了對於溫度補償次電路的需求。 $ 相對於具有GaAs基極層的傳統ΗΒΤ而言,具有 GalnAsN基極層的HBT已經改善了共同的射極輸出特徵。舉 例而言,具有GalnAsN基極層之HBT的偏移(0ff set)電壓和 拐曲(knee)電壓要比具有GaAs基極層的傳統HBT來得低 1288479 在一具體態樣中,電晶體是雙重異質接合雙極電晶體 (double heterojunction bipolar transistor , DHBT),其 組成基極的半導體材料乃異於製成射極和集極的半導體材 料。在DHBT的較佳具體態樣中,GalnAsN基極層可以由化 學式Ga^xIrixAs卜yNy來代表,集極是GaAs,並且射極是選 自 InGaP 、 AlInGaP 和 AlGaAs 。 本發明的另一個較佳具體態樣係關於HBT或DHBT,其 中降低了傳導能帶突峰的高度,同時降低了基極層的能帶 間隙(Egb)。傳導能帶突峰是由在基極/射極異質接合或基 極/集極異質接合處的傳導能帶不連續所引起的。藉由使 基極層的晶格匹配於射極和/或集極層而減少了晶格應變 ,則降低了傳導能帶突峰。此典型上是由控制基極層中之 氮和錮的濃度所做到的。基極層最好具有化學式Ga^ xInxAsWNy,其中X大約等於3y。 在具體怨樣中,基極可以在組成上加以分級,以製 出月b π間隙在集極處比較小而能帶間隙在射極處比較大之 刀級的旎帶間隙層。基極層的能帶間隙在基極層與集極接 觸的表面4 ’最好比在基極層與射極接觸的表面處低大約 20meV到大約12〇meV。基極層的能帶間隙更好則是從集極 到射極呈線性地變化越過基極層。 、外加氮和銦到GaAs半導體材料甲降低了材料的能帶間 隙…因此,Gai—xlrixASi—yNy半導體材料的能帶間隙要比GaAs 來仔低。在本發明之組成分級的Ga卜»卜具基極層中 基極層的能帶間隙在集極處減少得要比在射極處來得大 1288479 而,相較於GaAs越過基極層的能帶間隙而言,上述能 π間隙典型上平均減少大約l〇meV到大約。在一具 體態樣中,相較於GaAs越過基極層的能帶間隙而言,上述 月b π間隙典型上平均減少大約8〇mey到大約。在另 一具體態樣中,相較於GaAs越過基極層的能帶間隙而言, 上述能帶間隙典型上平均減少大約1〇meV到大約2〇〇meV。 此降低的能帶間隙導致具有組成分級之Gai·»卜具基 極層的HBT的打開電壓(vbe,Qn)要比具有GaAs基極層的HBT 來侍低,此乃因為Vbe,〇n中的主要決定者是基極中的固有 載子濃度。固有载子濃度(ni)由以下公式所計算: ni=NcNvexp(-Eg/kT) 在上述公式中,Nc是傳導能帶狀態的有效密度;Nv是 共價能帶狀態的有效密度;Eg是能帶間隙;τ是溫度;而k 是波錄曼节數。從公式可以看出基極中的固有載子濃度大 大地受到用於基極中之材料的能帶間隙所控制。 將基極層的能帶間隙從基極一射極界面的較大能帶間 隙分級到基極一集極界面的較小能帶間隙,此則引入了準 電場,其使電子加速越過npn雙極電晶體中的基極層。電 場增加了基極中的電子速度,減少了集極傳輸時間,此則 改善了 RF(radio frequency,射頻)表現以及增加了集極電 流增益(也稱為dc電流增益)。在具有重摻雜之集極層的 HBT情況中,dc增益(召心)乃受限於中性基極(η = ι)中的整 體再結合。dc電流增益可以由公式來估計: /5 dc « ^ r /Wb (l) 1288479 在公式(1)中,p是基極中之次要載子的平均速度^ 是基極中之次要載子的壽命,·而 ' 是基極的厚度。相較於 未分級的GalnAsN基極層而言,將具有GaInAsN基極層之 HBT中的基極層加以適當分級,由於增加電子速度的緣故 ,則導致;5 dc有顯著的增加。 為了達成在基極層厚度上加以分級的能帶間隙,基極 層乃製備成在基極層的第一表面處(靠.近集極)之銦和/或 氮的濃度要比在基極層的第二表面處(靠近射極)來得高。 銦和/或氮的含量變化最好是呈線性地變化越過基極層, 而造成線性分級的能帶間隙。摻雜物(例如碳)的濃度^整 個基極層中最好維持以不變。在—具體態樣中,‘ xInxASl_yNy基極層(例如DHBT的基極層)乃分級成在集極處 X和37大約等於〇.〇卜而在射極處乃分級成又和打大約 等於零。在另-具體態樣中,GaixIMsiA基極層從在基 極層與集極接觸的表面處χ值在大約〇 . 2到大約〇 ·⑽的範 圍,分級成在基極層與射極接觸的表面處χ值在大約Ο」 到零的範圍,前提是在基極層與集極接觸之表面處的X值 要比在基極層與射極接觸的表面處來得大。在此具體態樣 中,y在整個基極層中可以維持固定不變,或者可以加以 線性分級。當y是線性分級時,基極層從在基極層與集極 接觸的表面處y值在大約0.2到大約0 02的範圍,分級成 在^極層與射極接觸的表面處y值在大約Q1到零的範圍 ,前提是在基極層與集極接觸之表面處的y值要比在某極 層與射極接觸的表面處來得大。在一較佳的具體態樣二 1288479 X在集極處大约是0.06,並且線性分級成在射極處的大约 〇· 01。在一更佳的具體態樣中,X在集極處大約是〇· 〇6, 並且線性分級成在射極處的大約〇·〇1,同時y在整個基極 層中大約是0. 001。 在另一具體態樣中,本發明係一種形成分級之半導體 層的方法,此分級的半導體層從第一表面經過該層到第二 表面具有基本上線性分級的能帶間隙以及基本上固定不變 之摻雜X移動性的乘積。此方法包括·· (a)比較多個校正層的摻雜、移動性的乘積,其中每 一層係在沉積週期表之ΙΠ或v族原子的有機金屬化合物 或者沉積碳的w _化碳化合物當中卜者之明輕分的流 動速率下所形《,藉此決^形成基本上固定不變的推雜χ 移動!·生乘積所而要之有機金屬化合物和四_化碳的相對流 動速率;以及 ⑻在該相對流動速率下,將有機金屬化合物和四函 化碳化合物流動於一表面上,以形成基本上固定不變之摻雜 X移動性的乘積’而在沉精期間故 在整個分級之半導體二==流動速率’藉此形成 曰中基本上呈線性分級的能帶間隙。 基極層也可以對摻雜物加以分級,如此使得靠近隼極 的摻雜物濃度比較冑,έ & & 八 —射極異質接合。的厚度而逐漸減少到基極 種使料能帶突㈣到是在 f包或多個過渡層。可以採用具有低能帶間隙之挫; ⑻層、分級能帶㈣層、摻雜突峰或其组合的過 12 1288479 渡層,來使傳導能帶突峰達到最小。此外,—或多個晶格 匹配層可以存在於基極和射極之間或者基極和集極之間, 以減少材料在異質接合處的晶格應變。 本發明也提供—種製造贿和贿的方法。此方法包 括在η型摻雜的恤集極上長出由鎵、銦、朴氮所組成 的基極層。基極層可以採用内部和/或外部的碳來源來成 長’以提供摻雜碳的基極層。然後在基極層上長出η型摻 雜的射極層。使用内部和外部的碳來源以提供用於基極層 的碳摻雜物,可以幫助形成碳摻雜物濃度比較高的材料。 典型上,使用本發明的方法達到大約i 5xi〇iw到大約 7. 〇 1 ◦ cm的摻雜物程度。在—較佳的具體態樣中,以本 發明的方法可以達到大約3.QxlG1Wi|jM 7 Qxi〇i9cm_3 的換雜物程度。材斜φ p古Μ 材枓中更回的摻雜物濃度會降低材料的片 =阻和能帶間隙。因此,HBT和贿之基極層中的推雜物 濃度愈高,則元件的打開電壓就愈低。 本發明也提供一種由化擧$ Γ γ . χτ 、 裡田化予式GahInxAs卜yNy所代表的材 料,其中“口 y分別獨立地為大約h 〇χΐ〇_4到大約 2.〇Χΐ(Γΐ °Χ最好大約等於x和3y更好則是大約等於 0.01。在一具體態樣中,此材料乃摻雜以大約l 5xi〇i9cm_3 到大約7. 〇x1〇1W漢度的碳。在一特定的具體態樣中, 碳摻雜物的濃度是大約3.〇x1()1W到大約7GxiQlw。 降低打開電壓可以對於基於GaAs之有線和無線rf電 路的電壓預算做更好的管理,該等電路乃受制於標準的固 定電壓供應或者受制於電池輸出。降低打開電壓也可以改 13 1288479 變基於GaAs之HBT中之多種基極電流成分的相對大小。之 知已經顯示為接合溫度與施加應力兩者之函數的DC電流增 益穩定度,乃嚴重地依賴著基極電流成分的相對大小。低 的打開電壓所造成之逆向電洞注入的減少,係有利於元件 的溫度穩定度和長期可靠度。因此,具有高摻雜物濃度之 相對上沒有應變的Ga^Jr^Asi-yNy基極材料可以顯著提昇 基於GaAs之HBT和DHBT的RF表現。 【實施方式】 從底下本發明之較佳具體態樣的更特定敘述,本發明 前述和其他的目的、特色和優點將會變得明顯,該等較佳 的具體態樣乃圖解說明於所附的圖式,其中相似的參考字 元是指不同視圖中的相同部份。圖式未必是按照比例的, 而是強調示範本發明的原理。 ΠΗ族材料是晶格包括至少—種選自週㈣⑴⑴ 欄之元素以及至少一種撰白;两好 、 週』表V(A)攔之元素的半導體x=3y in GabxIrixASi-yNy. In a conventional HBT with GaAs, as the temperature increases, the emitter is injected to a higher degree, the recombination current of the inter-charge layer is higher, and the diffusion length in the base may be shorter, so the current gain is typical. It will be lowered. In the HBT towel with the GalnAsN base layer, as the temperature increases, a significant increase in current gain is found (about 3% increase per rc). This result is explained by the fact that the diffusion length increases with increasing temperature. If the electrons at the bottom of the band are limited to the state in which they are at least partially localized; Ping is expected to have such an effect, and as the temperature increases, they are thermally excited from the above state to other states in which electrons can more easily diffuse. . Therefore, designing the base layer with GalnAsN improves the temperature characteristics of the HBT of the present invention and reduces the need for a temperature compensated sub-circuit. $ HBT with a GalnAsN base layer has improved the common emitter output characteristics relative to conventional germanium with a GaAs base layer. For example, the offset (0ff set) voltage and the knee voltage of the HBT with the GalnAsN base layer are lower than the conventional HBT with the GaAs base layer. 1288479 In a specific aspect, the transistor is double A hetero heterojunction bipolar transistor (DHBT) whose semiconductor material is composed of a semiconductor material different from that of an emitter and a collector. In a preferred embodiment of the DHBT, the GalnAsN base layer can be represented by the chemical formula Ga^xIrixAs yNy, the collector is GaAs, and the emitter is selected from InGaP, AlInGaP, and AlGaAs. Another preferred embodiment of the invention is directed to HBT or DHBT, wherein the height of the conduction band peak is reduced while the energy band gap (Egb) of the base layer is reduced. The conduction band peak is caused by a discontinuity in the conduction band at the base/emitter heterojunction or the base/collector heterojunction. By reducing the lattice strain by matching the lattice of the base layer to the emitter and/or collector layers, the conduction band peaks are reduced. This is typically done by controlling the concentration of nitrogen and helium in the base layer. The base layer preferably has the chemical formula Ga^ xInxAsWNy, where X is approximately equal to 3y. In the specific grievances, the base can be graded in composition to produce a crevice gap layer with a relatively large knife-level gap at the emitter and a larger gap at the emitter. The energy band gap of the base layer is preferably about 20 meV to about 12 〇 meV lower than the surface of the base layer in contact with the collector. The energy band gap of the base layer is more linearly changed from the collector to the emitter across the base layer. The addition of nitrogen and indium to the GaAs semiconductor material reduces the band gap of the material... Therefore, the band gap of the Gai-xlrixASi-yNy semiconductor material is lower than that of GaAs. In the Gab»p-type base layer of the composition of the present invention, the energy band gap of the base layer is reduced at the collector by 1288479, compared to the energy of the GaAs over the base layer. In terms of the gap, the above-mentioned energy π gap is typically reduced by an average of about 10 〇 meV to about. In a physical aspect, the above-mentioned monthly b π gap is typically reduced by about 8 〇mey to about on average compared to the energy band gap of GaAs across the base layer. In another embodiment, the band gap is typically reduced by an average of about 1 〇meV to about 2 〇〇meV compared to the energy band gap of the GaAs across the base layer. This reduced band gap results in an open voltage (vbe, Qn) of the HBT having a graded Gai·» base layer that is lower than that of the HBT having a GaAs base layer, because Vbe, 〇n The main determinant is the inherent carrier concentration in the base. The intrinsic carrier concentration (ni) is calculated by the following formula: ni = NcNvexp (-Eg / kT) In the above formula, Nc is the effective density of the conduction band state; Nv is the effective density of the covalent band state; Eg is Can have a gap; τ is the temperature; and k is the number of the troughs. It can be seen from the equation that the inherent carrier concentration in the base is largely controlled by the band gap of the material used in the base. The energy band gap of the base layer is graded from the larger band gap of the base-emitter interface to the smaller band gap of the base-collector interface, which introduces a quasi-electric field that accelerates the electrons over the npn double The base layer in the polar crystal. The electric field increases the electron velocity in the base and reduces the collector transmission time, which improves RF (radio frequency) performance and increases the collector current gain (also known as dc current gain). In the case of HBTs with heavily doped collector layers, the dc gain (calling) is limited by the overall recombination in the neutral base (η = ι). The dc current gain can be estimated by the formula: /5 dc « ^ r /Wb (l) 1288479 In equation (1), p is the average velocity of the secondary carrier in the base ^ is the secondary load in the base The life of the child, and ' is the thickness of the base. The proper classification of the base layer in the HBT having the GaInAsN base layer compared to the unfractionated GalnAsN base layer results in a significant increase in 5 dc due to an increase in electron velocity. In order to achieve an energy band gap that is graded over the thickness of the base layer, the base layer is prepared such that the concentration of indium and/or nitrogen at the first surface of the base layer (by the near collector) is greater than at the base The second surface of the layer (near the emitter) is high. The change in the content of indium and/or nitrogen is preferably a band gap which changes linearly across the base layer to cause linear grading. The concentration of the dopant (e.g., carbon) is preferably maintained constant throughout the base layer. In a particular aspect, the 'xInxASl_yNy base layer (e.g., the base layer of the DHBT) is graded such that at the collector X and 37 are approximately equal to 〇. 而 and at the emitter are graded and the sum is approximately equal to zero. In another embodiment, the GaixIMsiA base layer is demarcated from a surface in contact with the collector at the base layer to a range of from about 0.2 to about 〇·(10), and is graded to be in contact with the emitter at the base layer. The χ value at the surface is in the range of Ο" to zero, provided that the X value at the surface where the base layer is in contact with the collector is larger than at the surface where the base layer is in contact with the emitter. In this particular aspect, y may remain fixed throughout the base layer or may be linearly graded. When y is linearly graded, the base layer has a y value ranging from about 0.2 to about 0 02 at the surface where the base layer is in contact with the collector, and is graded such that the y value at the surface where the gate layer is in contact with the emitter is A range of approximately Q1 to zero, provided that the y value at the surface where the base layer is in contact with the collector is greater than the surface at which the pole layer is in contact with the emitter. In a preferred embodiment 2, 1288479 X is approximately 0.06 at the collector and is linearly graded to approximately 〇 01 at the emitter. In a preferred embodiment, X is approximately 〇·〇6 at the collector, and is linearly graded to approximately 〇·〇1 at the emitter, while y is approximately 0.001 in the entire base layer. . In another embodiment, the invention is a method of forming a graded semiconductor layer having a substantially linearly graded energy band gap from the first surface through the layer to the second surface and substantially fixed The product of the doping X mobility. The method includes (a) comparing the product of doping and mobility of a plurality of correction layers, wherein each layer is among the organometallic compounds of the 沉积 or v group atoms of the deposition period or the w _ carbon compounds of the deposited carbon. The shape of the lighter is determined by the flow rate of the lighter, so as to form a substantially constant pusher χ move! The relative flow rate of the organometallic compound and the quaternary carbon; And (8) flowing the organometallic compound and the tetra-functionalized carbon compound on a surface at the relative flow rate to form a product of substantially constant doping X mobility, and during the grading period The semiconductor two == flow rate ' thereby forming a substantially linearly graded energy band gap in the crucible. The base layer can also classify the dopants such that the dopant concentration near the drain is relatively 胄, έ && The thickness is gradually reduced to the base species so that the material can be banded (four) to be in the f package or multiple transition layers. It is possible to use a low energy band gap; (8) layer, graded energy band (four) layer, doped peaks or a combination thereof to pass the 12 1288479 layer to minimize the conduction band peak. Additionally, - or a plurality of lattice matching layers may be present between the base and the emitter or between the base and the collector to reduce the lattice strain of the material at the heterojunction. The invention also provides a method of making bribes and bribes. The method includes growing a base layer composed of gallium, indium, and argon on the n-type doped shirt. The base layer can be grown using internal and/or external carbon sources to provide a carbon doped base layer. An n-type doped emitter layer is then grown on the base layer. The use of internal and external carbon sources to provide carbon dopants for the base layer can help to form materials with relatively high carbon dopant concentrations. Typically, a degree of dopant of from about i5 xi 〇 iw to about 7. 〇 1 ◦ cm is achieved using the method of the present invention. In a preferred embodiment, the degree of alteration of about 3.QxlG1Wi|jM 7 Qxi〇i9cm_3 can be achieved by the method of the present invention. The material concentration of the material is reduced by the concentration of the dopant in the material, which reduces the sheet resistance and band gap of the material. Therefore, the higher the concentration of the tamper in the base layer of HBT and bribe, the lower the opening voltage of the component. The present invention also provides a material represented by the chemical formulas $ Γ γ . χτ, 里田化予式 GahInxAs yNy, wherein "the mouth y is independently from about h 〇χΐ〇 _4 to about 2. 〇Χΐ (Γΐ °Χ is preferably about equal to x and 3y, more preferably about 0.01. In a specific aspect, the material is doped with carbon of about 15 〇 〇 i9 cm _ 3 to about 7. 〇 x 1 〇 1 W Han. In a particular embodiment, the concentration of carbon dopant is about 3. 〇 x1 () 1 W to about 7 Gxi Qlw. Lowering the turn-on voltage allows for better management of the voltage budget of GaAs-based wired and wireless rf circuits, such The circuit is subject to a standard fixed voltage supply or is subject to battery output. Lowering the turn-on voltage can also change the relative magnitude of the various base current components in a GaAs-based HBT. It has been shown to be both junction temperature and applied stress. The DC current gain stability of the function is heavily dependent on the relative magnitude of the base current component. The reduction of the reverse hole injection caused by the low open voltage is beneficial to the temperature stability and long-term reliability of the component. Therefore, the relatively unstrained Ga^Jr^Asi-yNy base material with high dopant concentration can significantly improve the RF performance of GaAs-based HBT and DHBT. [Embodiment] The preferred embodiment of the present invention from the bottom The above and other objects, features and advantages of the present invention will become more apparent from the aspects of the appended claims. The same parts in the drawings. The drawings are not necessarily to scale, but rather to demonstrate the principles of the invention. The steroidal material is a lattice comprising at least one element selected from the group (4)(1)(1) and at least one essay; Week s table V (A) block element of semiconductor

。在一具體態樣中,Ιπ—V族材料H 择材枓疋一種包括鎵、銦、珅 和氮的晶格。111 -V族姑祖县上. In a specific aspect, the Ιπ-V material H is selected from a crystal lattice including gallium, indium, antimony and nitrogen. 111-V family in Guzu County

兵材科最好可以由化學式G yNy來代表,其中义和y個別猸☆从4 nlnxASl_ , y個別獨立地為大約1.〇><1(^到大約 2.〇xl〇_hX更好則是大約 ]大、,勺 ^ ^ 0 、。在一最佳的具體熊樣 中,X和是大約〇. 。 〜 在此所用的「過渡;f . 日」(transitional layer)—饲县 指介於基極/射極異質接合之 °疋 間的層,並且具有使異皙垃 一妾曰之 異貝接合之傳導能帶突峰達到最小的 14 1288479 功能。使傳導能帶突峰達到最小的一種方法是使用一系列 的過渡層,其中在基極/集極的異質接合中,過渡層的能 帶間隙從最靠近集極的過渡層逐漸減低到最靠近基極的過 渡層。類似地,在射極/基極的異質接合中,過渡層的能 帶間隙從最靠近射極的過渡層逐漸減低到最靠近基極的過 渡層。使傳導能帶突峰達到最小的另一種方法是使用具有 分級之能帶間隙的過渡層。過渡層的能帶間隙可以藉由將 該層摻雜物濃度加以分級而分 a 刀敬舉例而言,過渡層的摻 雜物濃度可以在接近基極處較高,而在接近集極或射極處 逐漸地降低。另外可以選擇的是使用晶格應變,以提供且 有分級之能帶間隙的過渡層。舉例來說,過渡層可以^且 成上加以分級,以使接觸基極的表面有最小的晶格應變, 而增加接觸集極或射極之表面的晶格應變。使傳導能帶突 聲達到最小的另一種方法是使用具有摻雜物濃度突峰的過 渡層。使傳導能帶突峰達到最小的上述一或多種方法可以 用於本發明的順。適合本發明之HBT的-過渡層包括恤 、InGaAs 和 InGaAsN。 晶格匹配層是長在具有不同晶格常數之材料上的一層 。晶格匹配層典型上的厚度為大約500A或更小,並且^ 本上符合底下層的晶格常數。如果晶格匹配材料沒有肩變 ,則此導致介於底下層的能帶間隙和晶格匹配材料的能 間隙之間的能帶間隙。形成晶格匹配層的方法乃熟於此: 藝者所已知的,並且可以見⑨Ferry等人之「碎化嫁科技 」(Gailium Arsenide Techn〇iogy)的第 3〇3〜328 頁(】985 15 1288479 年’印第安那州Indianapolis的Howard W· Sams股份有 限A司出版),其所教導的併於此以為參考。適合本發明 之晶袼匹配層的一個材料範例是InGaP。 遏定組成之基極層的HBT和DHBT 本發明的HBT和DHBT可以使用適當之金屬有機化學氣 相〆冗積(metal organic chemical vapor deposition , MOCVD)的磊晶成長系統來製備。M〇CVD磊晶成長系統的適 當範例為AIXTR0N 2400和AIXTR0N 2600平台。在以本發 明方法所製備的HBT和DHBT中,典型而言,在當場去除吸 附的氧化物之後可以成長未摻雜的GaAs缓衝層。舉例而言 ’包含高濃度之η型摻雜物(例如摻雜物濃度大約 lxl〇18cm3到大約9><1018ciir3)的次集極層可以在大約7〇〇°c 的溫度下成長。具有低濃度之η型摻雜物(例如摻雜物濃度 大約5xl〇15cnr3到大約5xl〇16cm-3)的集極層可以在大約7〇〇 °c的溫度下成長於次集極層上。次集極和集極最好是GaAs 。次集極層典型的厚度為大約4〇〇〇A到大約6000A,而集 極層典型的厚度為大約3000A到大約5000A。在一具體態 樣中,次集極和/或集極中的摻雜物是矽。 晶格匹配的I nGaP穿隧層可以視需要選擇性地在典型 的成長條件下生長於集極上。晶格匹配層一般的厚度為大 約500A或更小,最好是大約200A或更小,並且其摻雜物 濃度為大約1 X1 〇16cnT3到大約1X 1 〇18ciir3。 一或多個過渡層可以視需要選擇性地在典型的成長條 件下生長於晶格匹配層上或集極上(如果沒有使用晶格匹 1288479 配層的話)。過渡層可以由n型摻雜的GaAs、„型摻雜的 InGaAs或η型摻雜的InGaAsN所製備。過渡層可以視需要 選擇性地在成分上或摻雜物上加以分級,或者可以包含^參 雜物的突峰。過渡層典型的厚度為大約75a到大約25A。 如果沒有使用晶格匹配層或過渡層,則在集極上成長推雜 碳的InGaAsN基極層。 基極層是在低於大約75(TC的溫度下成長,並且典型 上大約400A到大約1500A厚。在一較佳的具體態樣中, 基極層是在大約500°C到大約600°C的溫度下成長。摻雜碳 的InGaAsN基極層可以視需要選擇性地成長於過渡層上或 晶格匹配層上(如果沒有使用過渡層的話)。基極層可以使 用適當的鎵來源(例如三甲基鎵或三乙基鎵)、砷來源(例如 胂、三丁基胂或三甲基胂)、銦來源(例如三甲基銦)和氮來 源(例如氨或二甲基聯氨)來成長。偏好使用砷來源對鎵來 源的低莫耳比例。典型上,砷來源對鎵來源的莫耳比例是 小於大約3· 5。該比例更好是大約2· 〇到大約3· 〇。調整氮 和鋼來源的程度’以得到包括大約〇 〇1%到大約2〇%的銦和 大約0.01%到大約20%的氮之材料。在一較佳的具體態樣中 ,基極層的銦含量是氮含量的大約三倍。在一更佳的具體 態樣中,銦含量是大約1%,而氮含量是大約〇3%。在本發 明中,具有大約1· 5xl〇19cm_3到大約?· 之高碳摻 雜物?辰度的InGaAsN層,可以使用外部碳來源或有機金屬 來源(尤其是鎵來源)來獲得。外部碳來源的適當範例是四 溴化碳。四氯化碳也是有效的外部碳來源。 17 1288479 在基極和射極之間可以視需要選擇性地由n型摻雜的Armored materials can best be represented by the chemical formula G yNy, where Yihe y individual 猸 ☆ from 4 nlnxASl_ , y individually independently about 1. 〇 >< 1 (^ to about 2. 〇 xl 〇 _hX more The better is about the big, the spoon ^ ^ 0. In a best specific bear sample, X and is about 〇.. ~ "Transitional layer" used in the "transitional layer" Refers to the layer between the base/emitter heterojunction and has the 14 1288479 function of minimizing the conduction band peaks of the different meta-bonds. The smallest method is to use a series of transition layers in which the band gap of the transition layer is gradually reduced from the transition layer closest to the collector to the transition layer closest to the base in the heterojunction of the base/collector. Ground, in the heterojunction of the emitter/base, the energy band gap of the transition layer is gradually reduced from the transition layer closest to the emitter to the transition layer closest to the base. Another way to minimize the conduction band peak Is to use a transition layer with a graded energy band gap. The energy gap of the transition layer can be By stratifying the layer dopant concentration, for example, the dopant concentration of the transition layer can be higher near the base and gradually decrease near the collector or emitter. It is optional to use lattice strain to provide a graded energy gap with a transition layer. For example, the transition layer can be graded to have a minimum lattice strain on the surface of the contact base. Increasing the lattice strain of the surface contacting the collector or emitter. Another way to minimize the conduction band outburst is to use a transition layer with a peak of dopant concentration to minimize the conduction band peak. One or more methods can be used in the present invention. The transition layer of the HBT suitable for the present invention includes a shirt, InGaAs, and InGaAs N. The lattice matching layer is a layer that grows on a material having a different lattice constant. Typically, the thickness is about 500 A or less, and is consistent with the lattice constant of the underlying layer. If the lattice matching material has no shoulder change, this results in an energy band gap between the underlying layer and the energy of the lattice matching material. The band gap between the gaps. The method of forming the lattice matching layer is familiar to this: It is known to the artist, and can be seen in the third of the "Gailium Arsenide Techn〇iogy" by 9 Ferry et al. 〇 3 to 328 (in 1985 15 1288479, published by Howard W. Sams, Inc., Indianapolis, Indiana), which is hereby incorporated by reference. A material example of a wafer matching layer suitable for the present invention is InGaP. HBT and DHBT of the base layer of the depressing composition The HBT and DHBT of the present invention can be prepared using an appropriate epitaxial growth system of metal organic chemical vapor deposition (MOCVD). Suitable examples of M〇CVD epitaxial growth systems are the AIXTR0N 2400 and AIXTR0N 2600 platforms. In the HBT and DHBT prepared by the method of the present invention, an undoped GaAs buffer layer can be grown typically after removing the adsorbed oxide on the spot. For example, a sub-collector layer comprising a high concentration of n-type dopant (e.g., a dopant concentration of about lxl 〇 18 cm 3 to about 9 < 1018 ciir 3 ) can be grown at a temperature of about 7 ° C. A collector layer having a low concentration of n-type dopant (e.g., a dopant concentration of about 5 x 1 〇 15 cnr3 to about 5 x 16 〇 16 cm -3 ) can be grown on the sub-collector layer at a temperature of about 7 〇〇 ° C. The secondary collector and collector are preferably GaAs. The secondary collector layer typically has a thickness of from about 4 A to about 6000 A, while the collector layer typically has a thickness of from about 3000 A to about 5000 A. In a particular aspect, the dopant in the secondary collector and/or collector is germanium. The lattice matched I nGaP tunneling layer can be selectively grown on the collector under typical growth conditions as needed. The lattice matching layer typically has a thickness of about 500 A or less, preferably about 200 A or less, and a dopant concentration of about 1 X1 〇 16 cn T3 to about 1 X 1 〇 18 ciir 3 . One or more transition layers may optionally be grown on the lattice matching layer or on the collector under typical growth conditions as desired (if no lattice 1288479 layer is used). The transition layer may be prepared from n-doped GaAs, „type doped InGaAs or n-type doped InGaAsN. The transition layer may be selectively graded on the composition or dopant as needed, or may comprise ^ The peak of the dopant. The transition layer typically has a thickness of about 75a to about 25A. If a lattice matching layer or a transition layer is not used, the InGaAsN base layer of the carbon-doped carbon is grown on the collector. The base layer is low. It grows at a temperature of about 75 (TC) and is typically about 400 A to about 1500 A thick. In a preferred embodiment, the base layer is grown at a temperature of from about 500 ° C to about 600 ° C. The carbon-based InGaAsN base layer can optionally be grown on the transition layer or on the lattice matching layer (if no transition layer is used). The base layer can be made using a suitable gallium source (eg trimethylgallium or tris) Ethyl gallium), arsenic source (such as bismuth, tributyl hydrazine or trimethyl hydrazine), indium source (such as trimethyl indium) and nitrogen source (such as ammonia or dimethyl hydrazine) to grow. Preference is given to arsenic. Low molar ratio of source to gallium source. Typical The molar ratio of arsenic source to gallium source is less than about 3.5. The ratio is preferably about 2·〇 to about 3·〇. Adjusting the degree of nitrogen and steel source to obtain about 〇〇1% to about 2% by weight of indium and about 0.01% to about 20% of nitrogen. In a preferred embodiment, the indium content of the base layer is about three times the nitrogen content. In a better specific aspect The indium content is about 1%, and the nitrogen content is about 〇3%. In the present invention, an InGaAsN layer having a high carbon dopant of about 1.5×10 〇19 cm_3 to about Å can be used externally. A source of carbon or an organic metal source (especially a source of gallium) is available. A suitable example of an external carbon source is carbon tetrabromide. Carbon tetrachloride is also an effective source of external carbon. 17 1288479 Between the base and the emitter Need to be selectively doped by n-type

GaAs、η型摻雜的InGaAs或η型摻雜的InGaAsN長出一或 多個過渡層。在基極和射極之間的過渡層摻雜得比較輕( 例如大約5·〇χ1015(μιγ3到大約5.〇xl〇i6cnr3),並且可以視 需要選擇性地包含摻雜物的突峰。過渡層最好是大約25A 到大約75A厚。 射極層是在大約700°C的溫度下成長於基極上,或者 可以視需要選擇性地成長於過渡層上,並且典型上大約GaAs, n-type doped InGaAs or n-type doped InGaAsN grow one or more transition layers. The transition layer between the base and the emitter is doped lightly (e.g., about 5·〇χ1015 (μιγ3 to about 5.〇xl〇i6cnr3), and may optionally include a peak of the dopant. The transition layer is preferably from about 25 A to about 75 A. The emitter layer is grown on the base at a temperature of about 700 ° C or can optionally grow on the transition layer as desired, and is typically about

400A到大約1500A厚。射極層例如包括inGaP、AiinGaP 或AlGaAs。在一較佳的具體態樣中,射極層包括inGap。 射極層可以η型摻雜成大約1. 〇xl〇17cm-3到大約 9.〇xl〇17ciir3的濃度。包含高濃度的η型摻雜物(例如大約 l.〇xl018ciir3到大約9><1018αιΓ3)之GaAs的射極接觸層,可 以視需要選擇性地在大約700°C的溫度下成長於射極上。 典型而言,射極接觸層是大約1 000A到大約2〇〇〇A厚。 具有漸進的銦組成和高濃度之n型摻雜物(例如大約 5xl018cin3到大約5><1019cnr3)的InGaAs層乃成長於射極接 觸層上。此層典型上大約400A到大約ιοοοΑ厚。 範例1 為了示範降低基極層之能帶間隙和/或使射極/基極 異貝接合處之傳導能帶突峰達到最小的效果,比較了三種 不同之基於GaAs的雙極電晶體結構:GaAs射極/ GaAs基 極的BJT、InGaP / GaAs的HBT以及本發明之inGap / GalnAsN 的 DHBT。用於底下實驗的 inGaP/GaInAsN DHB丁 18 1288479 的一般代表結構乃圖解於圖1。由於基極和集極都是由 GaAs所形成,故在射極/基極界面處只有一個異質接合。 InGaP/GaAs HBT之GaAs基極層的能帶間隙要比In(Jap/ GalnAsN DHBT的基極層來得A。由於bjt的射 極、集極和基極都是由GaAs所做的,故其沒有異質接合。 所以使用GaAs BIT結構做為參考,以決定基極/射極界面 處的傳導能帶突峰對於InGaP/GaAs Ηβτ的集極電流特性 有何衝擊(如果有的話)。在圖1的隨中,係選擇InGaP 做為射極,而基極為Gai_xlMsi_A,此乃因為Μ#的能 帶間隙很寬,並且其傳導能帶對齊於Gai xlMsi—具基極 的傳導能帶。圖1之InGaP / GaInAsN耐和InGap /⑽ HBT的比較係用於決定具有較低能帶間隙的基極層對於集 極電流密度的效應。 用於底下討論的GaAs元件都具有以M0CVD長出之摻雜 反的基極層,其中摻雜物濃度從大約1 · $X1 〇i變化到 大約6.5xl〇i9cnr3,而厚度從大約5〇〇A變化到大約15〇〇人 ,以致基極片電阻〇^)在100Ω/□到4〇〇Ω/□之間。大 面積元件(L=75 # m><75 ν m)乃使用簡單的溼式蝕刻法來製造 ,並且在共同的基極架構中測試。逐量添加比較少量的銦 (X〜1%)和氮(y〜〇· 3%),以形成兩組不同的InGaP / GaInAsN DHBT。每一組的成長都已最佳化,以維持高而均勻的碳摻 雜物程度(>2.5xl〇i9cnr”、良好的移動性(〜85 cm2/v—s)以 及高的dc電流增益(Rsb〜300 Ω /□時乃>6〇)。400A to about 1500A thick. The emitter layer includes, for example, inGaP, AiinGaP, or AlGaAs. In a preferred embodiment, the emitter layer comprises inGap. The emitter layer may be doped n-type to a concentration of about 1. 〇xl 〇 17 cm -3 to about 9. 〇 xl 〇 17 ciir 3 . An emitter contact layer of GaAs comprising a high concentration of n-type dopant (e.g., about l. 〇xl018ciir3 to about 9><1018αιΓ3) can be selectively grown on the emitter at a temperature of about 700 ° C as needed. . Typically, the emitter contact layer is from about 1 000 A to about 2 A thick. An InGaAs layer having a progressive indium composition and a high concentration of n-type dopant (e.g., about 5xl018cin3 to about 5<1019cnr3) is grown on the emitter contact layer. This layer is typically about 400A to about ιοοο thick. Example 1 To demonstrate the effect of reducing the band gap of the base layer and/or minimizing the conduction band peaks at the emitter/base junction, three different GaAs-based bipolar transistor structures were compared: BJT of GaAs emitter/GaAs base, HBT of InGaP/GaAs, and DHBT of inGap / GalnAsN of the present invention. The general representative structure of inGaP/GaInAsN DHB butyl 18 1288479 for the bottom experiment is illustrated in Figure 1. Since both the base and the collector are formed of GaAs, there is only one heterojunction at the emitter/base interface. The band gap of the GaAs base layer of InGaP/GaAs HBT is better than that of In (Jap/ GalnAsN DHBT base layer. Since the emitter, collector and base of bjt are made of GaAs, there is no Heterojunction. So use the GaAs BIT structure as a reference to determine the impact of the conduction band peak at the base/emitter interface on the collector current characteristics of InGaP/GaAs Ηβτ, if any. In the middle, the InGaP is chosen as the emitter, and the base is extremely Gai_xlMsi_A, because the band gap of Μ# is very wide, and its conduction band is aligned with Gai xlMsi—the conduction band with the base. The comparison of InGaP / GaInAsN and InGap / (10) HBT is used to determine the effect of the base layer with a lower band gap on the collector current density. The GaAs elements used in the discussion below all have a doping inverse grown by M0CVD. The base layer, wherein the dopant concentration varies from about 1 · $X1 〇i to about 6.5xl 〇i9cnr3, and the thickness varies from about 5 〇〇A to about 15 ,, so that the base sheet resistance 〇 ^) Between 100Ω/□ and 4〇〇Ω/□. Large area components (L = 75 #m >< 75 ν m) were fabricated using a simple wet etch and tested in a common base architecture. A relatively small amount of indium (X~1%) and nitrogen (y~〇·3%) were added in portions to form two different sets of InGaP / GaInAsN DHBT. The growth of each group has been optimized to maintain a high and uniform carbon dopant level (>2.5xl〇i9cnr), good mobility (~85 cm2/v-s), and high dc current gain. (Rsb~300 Ω /□ is >6〇).

繪製具有相當的基極片電阻之GaAs / GaAs BJT、InGaP 1288479 / GaAs HBT 以及 InGaP/ GalnAsN DHBT 的典型 Gummel 圖, 並且重疊於圖 2。InGaP / GaAs HBT 和 GaAs / GaAs BJT 的 集極電流在超過電流的五個數量級(五個1 〇)都是無法分辨 的,直到有效串聯電阻的差異影響到電流一電壓特性為止 。另一方面,InGaP / GalnAsN DHBT的集極電流在很廣的偏 壓範圍中是GaAs / GaAs BJT和InGaP / GaAs HBT的兩倍, 此對應於1 · 78 A/cm2的集極電流密度(Jc)下的打開電壓減 少了 25· OmV。BJT中之低偏壓基極電流(n=2成分)所觀察 到的增加,乃與能帶間隙所驅動之空間電荷再結合的增加 一致。InGaP / GalnAsN DHBT中之集極電流的中性基極再結 合成分被驅動成高於InGaP / GaAs HBT,此乃因為集極電 流有所增加,以及次要載子壽命有所降低或者載子速度 (Inbr=Icwb/ ^ r)有所增加。以迄今所製備的inGaP / GalnAsN DHBT元件而言,基極片電阻為234Ω /□的元件已 經達到68的尖峰dc電流增益,此對應於打開電壓有 11.5mV的降低’而基極片電阻為303Ω/□的元件已經達到 66的尖峰dc電流增益,此對應於打開電壓有25· 〇mV的降 低。對於這幾種結構而言,此代表了已知最高的增益對基 極片電阻的比例(/3/Rsb〜0.2到0.3)。Gai_xInxAs卜yNy基極 的能帶間隙降低是觀察到之打開電壓降低的原因,如低溫 (77。1〇發光所示範的。0〔义1^測量顯示基極層的晶袼不匹 配是最小的(<250arcsec)。 在普及的限制中,以基極一射極電壓(Vbj為函數之雙 極電晶體的理想集極電流密度可以近似為: 20 1288479A typical Gummel plot of GaAs / GaAs BJT, InGaP 1288479 / GaAs HBT, and InGaP / GalnAsN DHBT with comparable base sheet resistance is plotted and overlapped in Figure 2. The collector currents of InGaP / GaAs HBT and GaAs / GaAs BJT are indistinguishable by more than five orders of magnitude (five 〇) in excess of current until the difference in effective series resistance affects the current-voltage characteristic. On the other hand, the collector current of InGaP / GalnAsN DHBT is twice that of GaAs / GaAs BJT and InGaP / GaAs HBT over a wide bias range, which corresponds to a collector current density of 1 · 78 A/cm 2 (Jc The opening voltage under ) is reduced by 25· OmV. The observed increase in the low bias base current (n = 2 component) in BJT is consistent with the increase in space charge recombination driven by the band gap. The neutral base recombination component of the collector current in InGaP / GalnAsN DHBT is driven higher than the InGaP / GaAs HBT due to an increase in collector current and a decrease in secondary carrier lifetime or carrier velocity. (Inbr=Icwb/^r) has increased. In the inGaP / GalnAsN DHBT device prepared so far, the element with a base sheet resistance of 234 Ω /□ has reached a peak dc current gain of 68, which corresponds to a 11.5 mV reduction in the turn-on voltage and a base sheet resistance of 303 Ω. The /□ component has reached a peak dc current gain of 66, which corresponds to a 25 〇mV reduction in the turn-on voltage. For these structures, this represents the ratio of the highest known gain to the base sheet resistance (/3/Rsb~0.2 to 0.3). The reduction of the energy band gap of the Gai_xInxAs yNy base is the cause of the observed decrease in the turn-on voltage, such as low temperature (77. 1 〇 luminescence is demonstrated. 0 [Sense 1 ^ measurement shows that the crystal layer mismatch of the base layer is the smallest (<250arcsec). In the popularization limit, the ideal collector current density of a bipolar transistor with a base-emitter voltage (Vbj as a function) can be approximated as: 20 1288479

Jc=(qDnn2ib/pbWb)eXp(qvbe/kT) 其中Jc=(qDnn2ib/pbWb)eXp(qvbe/kT) where

基極推雜和寬度; 擴散係數 ib 基極中的固有載子濃度 將nib表示成基極層能帶間隙(Egb)的函數,並且以基 極片電阻(Rsb)來改寫基極推雜和寬度的乘帛,則打開電壓 可以表示成基極片電阻的對數函數··Base push and width; diffusion coefficient ib The inherent carrier concentration in the base represents nib as a function of the base layer energy band gap (Egb), and the base plate resistance (Rsb) is used to rewrite the base push and The width of the multiplication, the open voltage can be expressed as a logarithmic function of the base sheet resistance.

Vbe-A ln(Rsb)+V〇 (3) 而 A=(kT/q) ⑷ 以及 V〇=Egb/q-(kT/qHMqZem/jc) (5) 其中1和Nv是傳導能帶和共價能帶中狀態的有效密度 ’而#是基極層中的主要載子移動性。 圖 3 繪出多個 in(jap/ GaAs ΗΒΤ、GaAs/ GaAs BJT 和 InGaP/GalnAsN DHBT當Κ·78 A/cm2時以基極片電阻為 函數的打開電壓。InGaP / GaAs HBT和GaAs / GaAs BJT沒 有任何傳導能帶突峰,其打開電壓都定性地呈現對於基極 片電阻有著如方程式(2)所期望之相同的對數依存關係。定 量而言,基極一射極電壓(ybe)隨著基極片電阻的變化並不 如方程式(3)所代表的來得劇烈(A=〇· 〇174mV,而非 〇· 0252mV)。然而,A所觀察到的降低乃與經過薄基極GaAs 雙極元件的準彈道(quasiballistic)傳輸一致。 與GaAs / GaAs BJT的特性做比較所引出的結論是·· InGaP / GaAs HBT之傳導能帶突峰的有效高度可以為零, 21 1288479 而集極電流展現理想的(Π=1)行為。因此,InGaP / GaAs HBT可加以設計成基本上不具有傳導能帶突峰。之前對於 AlGaAs/ GaAs HBT的研究也發現類似的結果。為了進一步 降低這些元件在固定之基極片電阻下的打開電壓,則需要 使用具有較低能帶間隙而仍維持傳導能帶連續性的基極材 料。可以使用Ga卜xInxAs卜yNy來降低Egb,同時維持接近晶 格匹配的情況。如圖3所見,兩組inGaP / GalnAsN DHBT 的打開電壓遵循著對基極片電阻的對數依存關係,此顯示 傳導能帶突峰大約為零。此外,相較於觀察的InGap / GaAs HBT和GaAs / GaAs BJT而言,其中一組的打開電壓向 下位移了 11.5mV而另一組向下位移了 25.〇mV(兩虛線)。 上述實驗顯示基於GaAs之HBT的打開電壓可以使用 InGaP/GalnAsN DHBT結構而下降到低於GaAs BJT的打開 電壓。低的打開電壓係透過兩個關鍵步驟所達成的。藉由 選擇基極和射極半導體材料(其傳導能帶大約在相同的能 P白),而首先使基極一射極界面最佳化,以抑制傳導能帶 大峰此乃使用InGaP或AlGaAs做為射極材料和Gaj\s做 為基極材料而成功地做到。然後藉由降低基極層的能帶間 隙而使打開電壓進一步地降低。此乃藉由添加銦和氮兩者 至基極層而達成,同時仍然維持整個Ηβτ結構的晶格匹配 。以適當的成長參數可以做到使集極電流密度增加兩倍, 而不會顯著犧牲基極摻雜或次要載子的壽命(Rsb = 234 Ω /口 時/5=68)。這些結果顯示使用GaixIiMSbNy材料提供了一 種降低基於GaAs # HBT和DHBT之打開電麼的方法。由於 22 1288479 在GaAs中併入銦和氮降低了材料的能帶間隙,則較大百分 比的銦和氮加入基極中,如果維持高的p型摻雜濃度,可 期望基於GaAs之HBT和DHBT的打開電壓有較大的降低。Vbe-A ln(Rsb)+V〇(3) and A=(kT/q) (4) and V〇=Egb/q-(kT/qHMqZem/jc) (5) where 1 and Nv are conduction bands and The effective density of the state of the valence band is 'and # is the main carrier mobility in the base layer. Figure 3 plots multiple in (jap/ GaAs ΗΒΤ, GaAs/GaAs BJT and InGaP/GalnAsN DHBT opening voltages as a function of base sheet resistance for Κ·78 A/cm2. InGaP / GaAs HBT and GaAs / GaAs BJT Without any conduction band peaks, the turn-on voltage is qualitatively present with the same logarithmic dependence as the equation (2) for the base sheet resistance. Quantitatively, the base-emitter voltage (ybe) The change in the base sheet resistance is not as dramatic as represented by equation (3) (A = 〇 · 〇 174 mV, not 〇 · 0252 mV). However, the observed decrease in A is compared to the thin base GaAs bipolar element. The quasi-ballistic (quasiballistic) transmission is consistent. The conclusion drawn from the comparison of the characteristics of GaAs / GaAs BJT is that the effective height of the conduction band peak of InGaP / GaAs HBT can be zero, 21 1288479 and the collector current is ideal. The behavior of (Π=1). Therefore, InGaP / GaAs HBT can be designed to have substantially no conduction band peaks. Previous studies on AlGaAs/GaAs HBT have found similar results. To further reduce these components in the fixed Base The turn-on voltage under the resistor requires the use of a base material with a lower band gap while still maintaining the continuity of the conduction band. Gab xInxAs yNy can be used to reduce Egb while maintaining near lattice matching. As can be seen, the turn-on voltage of the two inGaP / GalnAsN DHBTs follows the logarithmic dependence of the resistance of the base sheet, which shows that the conduction band peak is approximately zero. Furthermore, compared to the observed InGap / GaAs HBT and GaAs / GaAs In the case of BJT, the turn-on voltage of one of the groups is shifted downward by 11.5 mV and the other group is shifted downward by 25. 〇mV (two dashed lines). The above experiment shows that the opening voltage of the GaAs-based HBT can use the InGaP/GalnAsN DHBT structure. And falling below the turn-on voltage of the GaAs BJT. The low turn-on voltage is achieved through two key steps. By selecting the base and emitter semiconductor materials (the conduction band is about the same energy P white), First, the base-emitter interface is optimized to suppress the large peak of the conduction band. This is successfully done using InGaP or AlGaAs as the emitter material and Gaj\s as the base material. The band gap of the base layer further reduces the turn-on voltage. This is achieved by adding both indium and nitrogen to the base layer while still maintaining the lattice matching of the entire Ηβτ structure. It can be done with appropriate growth parameters. To increase the collector current density by a factor of two without significantly sacrificing the lifetime of the base doping or secondary carrier (Rsb = 234 Ω / port / 5 = 68). These results show that the use of GaixIiMSbNy material provides a way to reduce the turn-on power based on GaAs #HBT and DHBT. Since 22 1288479 incorporates indium and nitrogen in GaAs to reduce the band gap of the material, a larger percentage of indium and nitrogen are added to the base. If high p-type doping concentration is maintained, GaAs-based HBT and DHBT can be expected. The opening voltage is greatly reduced.

GalnAsN基極的能帶間隙降低乃假設是觀察到之打開 電壓降低的原因,已經由低溫(77。趵發光所確認。圖4比 較 InGaP/GalnAsN DHBT 和傳統的 InGaP/GaAs ΗΒΤ 的發 光光譜。來自InGaP/ GaAs HBT的基極層訊號是在比集極 還要低的能量(1.455eV對1.507eV),此係因為高摻雜程度 所帶來的能帶間隙窄化效應所致。來自InGaP / GaInAsN DHBT的基極層訊號出現在丨· 4〇8eV已被降低了,此係因為 能帶間隙窄化效應以及基極層中加入銦和氮所引起的基極 層能帶間隙降低所致。在此比較中,摻雜程度是相當的, 而相較於GaAs基極的能帶間隙而言,此建議基極層訊號位 置有47meV的降低可以相當於GaInAsN基極的基極層能帶 間隙降低。此發光訊號的位移與測得打開電壓降低45mv關 聯得很好。在沒有傳導能帶突峰的情形下,打開電壓的降 低可以直接關聯於基極層能帶間隙的降低。 圖5所示的DCXRD光譜示範了添加碳摻雜物和銦至 GaAs半導體的效應。圖5顯示來自inGaP / GaInAsN DHBT 以及相當基極厚度的標準InGaP/ GaAs HBT兩者的DCXRD 光譜。在InGaP / GaAs HBT中,基極層可看成是GaAs基板 尖峰之右手邊的肩部,大約對應於+90 arcsec的位置,此 乃由於4x1019cnr3的高濃度碳摻雜物所產生之拉伸應變的 緣故。由於添加了銦,此特別之InGaP / GalnAsN DHBT結 23 1288479 構的基極層尖峰是在-425 arcsec。一般而言,相關於 GalnAsN基極的尖峰位置是銦、氮和碳濃度的函數。添加 銦至GaAs則增加了壓細應變’而碳和氮兩者則以拉伸應變 來補償之。 當銦(和氮)加入摻雜碳的GaAs時維持高的p型摻雜程 度’乃需要小心的成長最佳化。可以由測得的基極片電阻 和基極厚度值的組合來獲得有作用之摻雜程度的粗略估計 。基極摻雜也可以藉由首先選擇性地蝕刻至基極層的頂端 ’然後得到Polaron C-V輪廓圖來加以確認。圖6比較 GaAs基極層和GalnAsN基極層的此種p〇iaron c—v摻雜輪 廓圖。在兩種情況中,摻雜程度超過了 3xl〇i9cm_3。 圖7A顯示另一種可選擇的DHBT結構,其具有固定組 成的Gal nAsN基極層,該基極層在射極/基極和集極/基 極的接合之間採用過渡層。此外,在過渡層和集極之間採 用晶格匹配的I nGaP穿隧層。The decrease in the energy band gap of the GalnAsN base is assumed to be the cause of the observed decrease in the turn-on voltage, which has been confirmed by low temperature (77. 趵 luminescence. Figure 4 compares the luminescence spectra of InGaP/GalnAsN DHBT and conventional InGaP/GaAs 。. The base layer signal of the InGaP/GaAs HBT is lower than the collector (1.455eV vs. 1.507eV) due to the band gap narrowing effect caused by the high doping level. From InGaP / The base layer signal of GaInAsN DHBT has been reduced by 丨·4〇8eV, which is caused by the band gap narrowing effect and the reduction of the base layer band gap caused by the addition of indium and nitrogen in the base layer. In this comparison, the degree of doping is comparable, and compared to the band gap of the GaAs base, the proposed base layer signal position has a 47 meV reduction which can be equivalent to the base layer band gap of the GaInAsN base. Decrease. The displacement of this illuminating signal is well correlated with the measured opening voltage drop of 45mv. In the absence of a conduction band peak, the reduction of the opening voltage can be directly related to the reduction of the band gap of the base layer. DCXRD The spectrum demonstrates the effect of adding carbon dopants and indium to GaAs semiconductors. Figure 5 shows DCXRD spectra from both InGaP / GaInAsN DHBT and standard InGaP/GaAs HBTs of comparable base thickness. In InGaP / GaAs HBT, base The layer can be seen as the shoulder on the right hand side of the GaAs substrate spike, approximately corresponding to the position of +90 arcsec, due to the tensile strain produced by the high concentration carbon dopant of 4x1019cnr3. In particular, the base layer peak of the InGaP / GalnAsN DHBT junction 23 1288479 is at -425 arcsec. In general, the peak position associated with the base of the GalnAsN is a function of the concentration of indium, nitrogen and carbon. Adding indium to GaAs increases The compact strain 'and both carbon and nitrogen are compensated by tensile strain. Maintaining a high p-type doping level when indium (and nitrogen) is added to the carbon doped GaAs requires careful growth optimization. A rough estimate of the degree of doping of the action can be obtained from a combination of measured base sheet resistance and base thickness values. Base doping can also be obtained by first selectively etching to the top of the base layer'. Polaron The CV profile is confirmed. Figure 6 compares the p〇iaron c-v doping profile of the GaAs base layer and the GalnAsN base layer. In both cases, the doping level exceeds 3xl〇i9cm_3. Another alternative DHBT structure is shown having a fixed composition of Gal nAsN base layers that employ a transition layer between the emitter/base and collector/base junctions. In addition, a lattice-matched I nGaP tunneling layer is employed between the transition layer and the collector.

UligL成分級之基極層的DHBT 具有組成分級之基極層的DHBT中的所有層,可以類似 於具有固定組成之基極層的DHBT的方式成長,例外的是從 電晶體之一接合經過基極層到另一接合而做為分級能帶間 隙的基極層。舉例而言,如果沒有使用晶袼匹配層或過渡 層’則摻雜碳且能帶間隙分級的GaInAsN基極層可以長在 集極上。摻雜碳且分級的Gal nAsN基極層可以視需要選擇 1*生地生長於過渡層上或晶格匹配層上(如果沒有使用過渡 層的話)。基極層可以在低於大約750〇c的溫度下成長,並 24 1288479 且典型上大約400A到大約1500A厚。在一具體態樣中, 基極層是在大約500°C到大約600°C的溫度下成長。基極層 可以使用適當的鎵來源(例如三甲基鎵或三乙基鎵)、石申來 源(例如胂、三(三級丁基)胂或三曱基胂)、銦來源(例如三 曱基銦)和氮來源(例如氨、二甲基聯氨或三級丁基胺)來成 長。偏好使用砷來源對鎵來源的低莫耳比例。典型上,石申 來源對鎵來源的莫耳比例是小於大約3· 5。該比例更好是 大約2 · 0到大約3 · 0。可以調整氮和銦來源的程度,以得 到其中111族元素是大約〇· 〇1 %到大約2〇%的銦以及v族元 素疋大約0 · 01 %到大約2 0 %的氮之材料。在一特定的具體態 樣中’ III族元素銦的含量從基極/集極接合處的大約1〇% 到20%變化到基極/射極接合處的大約〇· %到5%,並且v 族元素氮的含量基本上是固定在大約〇·3%。在另一具體態 樣中’基極層的銦含量是氮含量的大約三倍。如之前所討 論的具有固定組成之InGaAsN基極層,相信具有大約 1· 5xl〇i9cnr3到大約7· 0x10i9cnr3之高碳摻雜物濃度的 InGaAsN層除了鎵來源外還可以再使用外部碳來源(例如四 鹵化碳)來獲得。使用的外部碳來源例如可以是四溴化碳 。四氯化碳也是有效的外部碳來源。 由於當成銦來源氣體來使用的有機銦化合物對 InGaAsN基極層所貢獻之碳摻雜物的量,乃不同於當成鎵 來源氣體來使用的有機鎵化合物,故在成長基極層的期間 ’典型上會調整碳摻雜物來源氣體的流動速率,如此以於 組成分級之InGaAsN基極層中維持固定不變的碳摻雜濃度 25 1288479 在具體恶樣中,組成分級的基極層上之碳來源氣體的 流動速率變化乃使用底下所述的方法來決定。 /或分級導體層的磁-三甲基錮來源漭動球率之校正裎序 製備至少兩組校正用HBT,其中每一組包含至少兩個 成員(可以使用贿來代替HBT)。所有校正用耐的基極 層厚度理想上是相同的,但這並非一項要求,並且每一個 HBT具有固定不變的組成,例如固定組成#⑽副或 InGaAs基極層和在該層中都固定不變的碳摻雜物濃度。每 -組是在不同於另-組的族添加物(例如ιπ族用 銦或V族用氮)之來源氣體流動速率下成&,如此每一組的 成員具有不同於別組成員的鎵、銦、砷和氮組成。舉例來 說,採用銦做為影響能帶間隙分級的添加物。特定組的每 一個成員係於不同的外部碳來源(例如四演化碳或四氯化 碳)流動速率下成長,所以特定組的每一個成員具有不同 的碳推雜物程度。決定每一個成員之摻雜X移動性的乘積 ’並且對碳來源的流動速率加以作圖。每一組之成員的摻 雜X移動性的乘積乃與碳來源氣體流動速率成比例地變化 。五組ΗΒΤ之摻雜X移動性的乘積對四漠化碳的流動速率 乃繪於圖8。另外可以選擇的是每一組校正用膽或可藉 由隹持□定机動速率的石厌來源氣體(例如四漠化碳)而形成 ’並且每-組中的個別樣品或可在相對於其他來源氣體的 流動速率下以不㈣m族或ν族添加物流動速率來形成 26 1288479 獲得固定的摻雜X移動性 ♦ 來源氣體的流動速率,乃辟由在積固^之石厌來源氣體對於姻 劃-條線橫越圖8(例如4='的摻雜x移動性乘積處 U巧如條+仃於x軸的線)來得到。 與每一組直線交又的地方木㈣此線 體流動速率時獲得此养雜、/ 該組的鋼來源氣 “I雜x移動性之乘積值所需的外部碳來 邱、:“。對於—固定之摻雜X移動性的乘積值而言,外 心厌來源流動速率_來源氣體流動速率騎於圖9。不同 抬:移動J·生的乘積可以相同方式繪出類似的線。 每個ΗΒΤ的集極電流乃繪成基極—射極 數’並且所得曲線則與具有⑽基極層而其他皆(與= 較的該組成員相同< ΗΒΤ(例如具有相同的摻雜物濃度、相 同=基極、射極和集極層厚度…等等)的圖形做比較。在 特疋集極電流處的曲線之間的電壓差別是基極一射極電壓 be的改艾(△ Vbe),此乃歸因於基極層的形成期間所添加的 钔和氮所造成之基極層能帶間隙較低的緣故。圖1 〇顯示具 有GalnAsN基極層之JJBT和具有GaAs基極層之HBT的集極 “ L 乂 Vbe為函數的圖形。兩曲線之間所劃的水平箭頭是 Δ Vbe。將所有組別的每個成員的△ vbe加以決定,並對碳 來源氣體流動速率加以繪圖。用於形成圖8的五組HBT之 每成員的△ vbe對四溴化碳流動速率乃繪於圖π。注意 到一組成員的△ Vbe跨越了該組一範圍的△ Vbe,此範圍可 以找出最適合的直線。這些直線則用於決定(内插)或許可 使用特定組別的相同銦來源氣體流動速率但碳來源氣體流 動速率異於該組其他成員而成長之HBT的△ Vbe。 27 1288479 、友對於固疋之摻雜x移動性的乘積而言,△ vbe係以銦來 :原氣體流動逮率為函數呈線性地變化,就如當固定之摻雜 移動性乘積的内插△ Vbe繪成銦來源氣體流動速率的函數 時所可以看到的。圖12顯示用於圖11之五組的此種圖形 〇 圖所不的圖形乃用於決定在基極/射極和基極/集 ㈣:合心导到想要之AVbe所需要的銦來源氣體流動速率:、 一决疋了銦來源氣體的流動速率,則使用圖g來決定在 此=來源氣體流動速率下所需的碳來源氣體流動速率,以 ,得所要之摻雜物X移動性的乘積。依照相同的程序以決 疋在基極/集極接合處所要的銦來源氣體流動速率和碳來 源乳體流動速率,以於組成分級的以化杬或以丨以⑽層中 維持所要固定的摻雜物X移動性乘積。#基極層從基極/ 集極接合成長至基極/射極接合時,銦來源氣體流動速率 和碳來源氣體流動速率乃相對於鎵和砷的程度而線性地變 化到這些接合處之這些來源氣體所決定的值,以獲得具有 所要之能帶間隙等級的線性分級基極層。 範例2 用於底下討論的GaAs元件都具有以M〇CVD長出之摻雜 碳的基極層,其中摻雜物濃度從大約3〇xl〇19cnr3變化到 大約5.〇xl〇i9cm_3,而厚度從大約5〇〇A變化到大約15〇〇入 ,以致基極片電阻(Rsb)在100Q/□到65〇ω/□之間。大 面積元件(L=75 // mx 75 // m)乃使用簡單的溼式蝕刻法來製造 ,並且在共同的基極架構中測試。逐量添加比較少量的銦 28 1288479 (x〜1%到6%)和氮(y〜〇· 3%),以形成兩組不同的InGap / GalnAsN DHBT。每一組的成長都已最佳化,以維持高而均 勻的碳摻雜物程度(>2. 5><1019cnr3)、良好的移動性(〜的 cmVV-s)以及高的dc電流增益(Rsb~300 Q/□時乃>6〇)。用 於底下實驗而具有組成分級之GalnAsN基極層的DHBT結構 乃顯示於圖13。具有組成分級的基極層之另外可以選擇的 DHBT結構乃顯示於圖7B和7C。用於底下實驗而具有固定 組成之GalnAsN基極層的DHBT結構乃顯示於圖u供比較 〇 圖15顯示具有相當的打開電壓和基極片電阻的固定基 極之DHBT和分級基極之DHBT的Gummel圖。分級基極結構 中之基極電流的中性基極成分乃顯著較低,其展現的尖峰 dc電流增盈可以是固定基極結構的兩倍以上。圖16比較 類似而有厚度變化之固定和分級的DHBT結構以基極片電阻 為函數的dc電流增益。增益對基極片電阻的比例增加是很 明顯的。雖然DHBT之增益對基極片電阻的比例乃視所用的 成長條件和整體結構的特定細節而定,但是已經觀察到具 有分級基極層之DHBT的dc電流增益要比具有固定基極層 之DHBT —致增加50%到1〇〇%。 9 圖17和18比較分級基極結構和兩個固定基極結構的 Gummel圖和增益曲線。第一個固定基極結構的基極組成對 應於分級基極在基極/射極接合處的基極層組成。第二個 固定基極結構的基極組成對應於分級基極在基極/集極接 合處的基極層組成。分級基極結構的打開電壓乃介於兩個 29 1288479 終點結構之間,不過朝向基極/射極終點方向加權。分級 基極結構的dc電流增益要比終點結構高出50%到95%,此 顯不dc電流增益的大部分增加係來自於電子速度的增加。 使用HP 8510C參數分析器在2指、4/zmx4//m射極面 積的70件上進行晶圓上的FF測試。使用斷路和短路結構去 除嵌埋的塾寄生,以及使用小訊號電流增益(H21)之-20dB/10的斜率來外插電流增益的切斷頻率(ft)。圖19綜 合了兩種結構上的ft與集極電流密度(Jc)的依附關係。圖 20圖解說明了在一特定偏壓點下小訊號增益對頻率的關係 。隨著Jc增加以及基極過渡時間(tj開始在整個過渡時間 中扮演限制的角色,儘管分級基極結構的基極厚度較大( 固定不變的基極層是60nm厚,而分級的基極層是8〇nm厚) ,分級基極結構的ft仍變得顯著大於固定組成的結構。 6〇nm之固定組成GalnAsN基極的尖峰ft是53 GHz,而 80nm之組成分級GalnAsN基極的尖峰ft是6〇 GHz。因此, 電流增益的切斷頻率增加13%。 為了好好比較具有固定和分級之GaInAsN基極層的 DHBT與傳統之GaAs HBT的RF結果,圖19的匕數值;成 可以施加於電晶體之零輸入電流崩潰電壓的函數。 此圖與引述文獻之傳統GaAs HBT的尖峰或近尖峰f *數值 做比較。預期傳統之GaAs HBT的ft數值分布相當廣,因 為此資料彙編自使用不同蠢晶結構、元件尺寸和測試條件 的許多組,並且只是要給出目前工業標準的概況。Βν^。經 常必須由引述的集極厚度來估計,而假設有如圖2 1所示的 30 1288479 =厚度a)、BVeb。和Βν“。之間的關係”亦如圖2i所示 M⑽之預期依存關係的三個簡單計算,其假設 Γ:=之空間電荷層的過渡時間係藉由電子飽和 τ速度(vs)而早純地關聯於Xc。在基線計算中,如同 1 000A GaAs 基極 > μ 丄 执、 9之M〇nte—Car!〇計算所預期的,τ b假 為· 115 ps並且剩餘之射極和集極過渡時間的總和( le+lc)則視為 0·95 ps。The DHBT of the base layer of the UligL component has all the layers of the DHBT constituting the graded base layer, which can be grown in a manner similar to the DHBT of the base layer having a fixed composition, with the exception of bonding from one of the transistors to the base. The pole layer is joined to the other as a base layer with a graded energy gap. For example, if a germanium matching layer or transition layer is not used, the GaInAsN base layer doped with carbon and capable of band gap classification may grow on the collector. The carbon-doped and graded Gal nAsN base layer can optionally be grown on the transition layer or on the lattice matching layer if desired (if no transition layer is used). The base layer can be grown at temperatures below about 750 〇c and is typically 24 1288479 and typically about 400A to about 1500A thick. In one embodiment, the base layer is grown at a temperature of from about 500 ° C to about 600 ° C. The base layer may be of a suitable gallium source (eg, trimethylgallium or triethylgallium), a Shishen source (eg, lanthanum, tris(tertiary butyl) ruthenium or tridecyl ruthenium), an indium source (eg, triterpenoid) Base indium) and nitrogen sources (such as ammonia, dimethyl hydrazine or tertiary butylamine) to grow. Preference is given to using a low molar ratio of arsenic source to gallium source. Typically, the ratio of the source of the Shishen source to the gallium source is less than about 3.5. The ratio is preferably from about 2 · 0 to about 3 · 0. The extent of the nitrogen and indium sources can be adjusted to obtain a material in which the Group 111 element is from about 1% to about 2% indium and the v-factor element is from about 0.01 to about 20% of nitrogen. In a particular embodiment, the content of 'Group III element indium varies from about 1% to 20% at the base/collector junction to about 〇% to 5% at the base/emitter junction, and The nitrogen content of the v group element is substantially fixed at about 〇·3%. In another embodiment, the indium content of the base layer is about three times the nitrogen content. As discussed previously with a fixed composition of InGaAsN base layer, it is believed that an InGaAsN layer having a high carbon dopant concentration of about 1.5×1 〇i9cnr3 to about 7.5×10i9cnr3 can reuse an external carbon source in addition to the gallium source (eg, Tetrahalide carbon) is obtained. The external carbon source used may for example be carbon tetrabromide. Carbon tetrachloride is also an effective source of external carbon. The amount of carbon dopant contributed to the InGaAsN base layer by the organic indium compound used as the indium source gas is different from the organogallium compound used as the gallium source gas, so during the growth of the base layer The flow rate of the carbon dopant source gas is adjusted so as to maintain a constant carbon doping concentration in the graded InGaAsN base layer. 25 1288479 In a specific evil sample, the carbon on the graded base layer is formed. The change in flow rate of the source gas is determined using the method described below. / or the order of the magneto-trimethyl hydrazine source of the graded conductor layer. At least two sets of calibration HBTs are prepared, each of which contains at least two members (a bribe can be used instead of HBT). The thickness of the base layer for all calibrations is ideally the same, but this is not a requirement, and each HBT has a fixed composition, such as a fixed composition #(10) pair or an InGaAs base layer and in both layers. A constant carbon dopant concentration. Each group is formed at a source gas flow rate different from that of another group (for example, a group of indium or a group of nitrogen for group V), such that members of each group have gallium different from members of other groups. Indium, arsenic and nitrogen. For example, indium is used as an additive that affects the band gap classification. Each member of a particular group grows at a different external carbon source (e.g., four evolutionary carbon or carbon tetrachloride) flow rate, so each member of a particular group has a different degree of carbon inclusions. The product of the doping X mobility of each member is determined and the flow rate of the carbon source is plotted. The product of the doping X mobility of the members of each group varies in proportion to the carbon source gas flow rate. The flow rate of the product of the doping X mobility of the five groups of bismuth to the carbonized carbon is shown in Fig. 8. Alternatively, each set of calibration biliary or may be formed by holding a stone source gas (eg, four desertified carbon) that determines the maneuver rate, and individual samples in each group may be relative to the other The flow rate of the source gas is formed by the flow rate of the (four) m or ν group additive. 26 1288479 Obtaining a fixed doping X mobility ♦ The flow rate of the source gas is derived from the gas source in the accumulation The stroke-strip is obtained by traversing Figure 8 (e.g., the line of the doping x mobility product of 4 = ', such as the bar + the line on the x-axis). The place where the line is crossed with each group (4) The body flow rate is obtained when the nutrient, / the steel source gas of the group "the external carbon required for the product value of the I heterogeneous mobility is Qiu,". For the product value of the fixed doping X mobility, the external anaesthetic source flow rate _ source gas flow rate is shown in Figure 9. Different Lift: The product of moving J·sheng can draw similar lines in the same way. The collector current of each ΗΒΤ is plotted as the base-emitter number' and the resulting curve is the same as having the (10) base layer and the others (the same as the group of = = ΗΒΤ (for example with the same dopant) The graphs of the concentration, the same = base, emitter and collector layer thickness, etc. are compared. The voltage difference between the curves at the characteristic collector current is the change of the base-emitter voltage be (△ Vbe), which is attributed to the lower band gap of the base layer caused by the addition of germanium and nitrogen during the formation of the base layer. Figure 1 shows the JJBT with the base layer of GalnAsN and the base of GaAs. The collector of the layer HBT "L 乂Vbe is a graph of the function. The horizontal arrow drawn between the two curves is Δ Vbe. The Δ vbe of each member of all groups is determined, and the carbon source gas flow rate is determined. Plot. The Δvbe versus carbon tetrabromide flow rate for each member of the five groups of HBTs used in Figure 8 is plotted in Figure π. Note that the ΔVbe of a group of members spans a range of ΔVbe for this set, this range You can find the most suitable straight line. These lines are used to decide (interpolate) Allows the use of a specific group of indium source gas flow rates but the carbon source gas flow rate is different from that of the other members of the group. Δ Vbe. 27 1288479, for the product of the solid doping x mobility, Δ vbe is indium: the original gas flow rate is linearly varied, as can be seen when the interpolated ΔVbe of the fixed doping mobility product is plotted as a function of the indium source gas flow rate. Figure 12 shows that the pattern used for the five groups of Figure 11 is used to determine the source of indium required at the base/emitter and base/set (4): to the desired AVbe. Gas flow rate: Once the flow rate of the indium source gas is determined, use Figure g to determine the carbon source gas flow rate required at this = source gas flow rate to obtain the desired dopant X mobility. According to the same procedure, the indium source gas flow rate and the carbon source milk flow rate required at the base/collector junction are determined to maintain the desired composition in the layer (10). Fixed dopant X shift Productivity. When the base layer grows from the base/collector junction to the base/emitter junction, the indium source gas flow rate and the carbon source gas flow rate vary linearly with respect to the extent of gallium and arsenic to these junctions. The values determined by these source gases are used to obtain a linear graded base layer having the desired band gap level. Example 2 The GaAs elements used in the discussion below all have a carbon-doped base grown by M〇CVD. a layer in which the dopant concentration varies from about 3〇xl〇19cnr3 to about 5.〇xl〇i9cm_3, and the thickness varies from about 5〇〇A to about 15〇〇, so that the base sheet resistance (Rsb) is at 100Q /□ to 65〇ω/□. Large area components (L = 75 // mx 75 // m) were fabricated using a simple wet etch and tested in a common base architecture. A small amount of indium 28 1288479 (x~1% to 6%) and nitrogen (y~〇·3%) were added in portions to form two different sets of InGap / GalnAsN DHBT. The growth of each group has been optimized to maintain a high and uniform carbon dopant level (>2.5><1019cnr3), good mobility (~cmVV-s), and high dc current Gain (Rsb~300 Q/□ is >6〇). The DHBT structure having the GalnAsN base layer of the compositional composition for the bottom experiment is shown in Fig. 13. An alternative DHBT structure having a base layer of compositional composition is shown in Figures 7B and 7C. The DHBT structure of the GalnAsN base layer with a fixed composition for the bottom experiment is shown in Figure u for comparison. Figure 15 shows the DHBT of the fixed base with a comparable open voltage and base sheet resistance and the DHBT of the graded base. Gummel map. The neutral base component of the base current in the graded base structure is significantly lower, exhibiting a peak dc current gain that can be more than twice that of the fixed base structure. Figure 16 compares the dc current gain as a function of the base plate resistance for a fixed and graded DHBT structure with similar thickness variations. The increase in the ratio of the gain to the base sheet resistance is significant. Although the ratio of the gain of the DHBT to the resistance of the base sheet depends on the growth conditions used and the specific details of the overall structure, it has been observed that the DHBT with a graded base layer has a dc current gain that is better than a DHBT with a fixed base layer. - Increase by 50% to 1%. 9 Figures 17 and 18 compare the Gummel plot and gain curve for a graded base structure and two fixed base structures. The base composition of the first fixed base structure corresponds to the base layer of the graded base at the base/emitter junction. The base composition of the second fixed base structure corresponds to the base layer of the graded base at the base/collector junction. The turn-on voltage of the graded base structure is between the two 29 1288479 end structures, but is weighted towards the base/emitter end. The dc current gain of the graded base structure is 50% to 95% higher than the end structure, and most of this increase in dc current gain is due to an increase in electron velocity. On-wafer FF testing was performed on 70 pieces of 2-finger, 4/zmx4//m emitter area using the HP 8510C parametric analyzer. The open and shorted structures are used to remove the embedded mistletoe and the cutoff frequency (ft) of the current gain is extrapolated using a slope of -20 dB/10 of the small signal current gain (H21). Figure 19 combines the dependence of ft and collector current density (Jc) on the two structures. Figure 20 illustrates the relationship of small signal gain versus frequency at a particular bias point. As Jc increases and the base transition time (tj begins to play a limiting role throughout the transition time, although the base thickness of the graded base structure is large (the fixed base layer is 60 nm thick, and the graded base) The layer is 8〇nm thick), the ft of the graded base structure still becomes significantly larger than the structure of the fixed composition. The fixed peak of the 6〇nm fixed composition of the GalnAsN base is 53 GHz, and the peak of the 80nm composition is graded GalnAsN base. Ft is 6 〇 GHz. Therefore, the cutoff frequency of the current gain is increased by 13%. In order to compare the RF results of the DHBT with the fixed and graded GaInAsN base layer and the conventional GaAs HBT, the 匕 value of Figure 19 can be applied. This is a function of the zero-input current breakdown voltage of the transistor. This figure is compared with the peak or near-peak f* values of the traditional GaAs HBT quoted in the literature. It is expected that the ft value distribution of conventional GaAs HBTs is quite extensive because this data is compiled from use. Many groups of different stupid crystal structures, component sizes and test conditions, and only to give an overview of current industry standards. Βν^. Often must be estimated from the quoted collector thickness, assuming 301288479 = thickness shown in FIG. 2 1 a), BVeb. And the relationship between Βν "." also shows three simple calculations of the expected dependence of M(10) as shown in Fig. 2i, which assumes that the transition time of the space charge layer of Γ: = is earlier by the electron saturation τ velocity (vs) Purely associated with Xc. In the baseline calculation, as expected from the calculation of 1 000 A GaAs base > μ 丄, 9 M〇nte-Car! ,, τ b is false · 115 ps and the sum of the remaining emitter and collector transition times (le+lc) is considered to be 0·95 ps.

—審視圖21顯示:雖然固定組成之⑽⑽的匕並未 完全位於傳統基於GaAS之騰的預期範圍之外,不過其顯 然是在該分布的下端。分級的基極結構則有顯著的改善。 第-個汁异(:b減少為2/3的基線)建議:基極過渡時間相 對於固定組成的結構而言乃降低大約⑽。相較於固定組 成的基極層而t,此顯示載子速度在分級的基極層中達到 兩倍的增加,此係因為載子速度的兩倍(2x)增加配合基極 厚度增加的33%乃預期導出rb減少為1/2 χ 4/3 = 2/3。- Review view 21 shows that although the fixed composition of (10) (10) is not completely outside the expected range of the traditional GaAS-based, it is clearly at the lower end of the distribution. There is a significant improvement in the graded base structure. The first juice difference (:b is reduced to a 2/3 baseline) suggests that the base transition time is reduced by approximately (10) relative to the structure of the fixed composition. Compared to the base layer of the fixed composition, t, this shows that the carrier velocity doubles in the graded base layer, which is due to the increase in the carrier's thickness by two times (2x). % is expected to reduce the export rb to 1/2 χ 4/3 = 2/3.

第三個計算(rb減少11/3以及(re+rc)減少為1/2的基 線)則近似出採用薄的和/或分級基極結構以及具有改善 之元件佈局和尺寸(以使r b、r e和r c達到最小)下的情形 範例3 為了改進放大器效率以及因而降低操作電壓和延長電 池壽命,故想要減低偏移電壓(VCE sat)和拐曲電壓(Vk)。減 低偏移電壓的一種方法是使基極/射極和基極/集極二極 體對之打開電壓的不對稱性達到最小。雖然集極能帶間隙 31 1288479 為寬的DHBT已經顯示可產生 導致較高的Vk並且降低效率 極異質接合處的位能阻障。 低的VCE,sat值,但是實際上此 ,此乃因為難以控制基極/集 插入具有高能帶間隙的薄層(穿隧集極),則允許同時 降低vCE,sat和vk,而改善了元件的效率。圖22顯示具有分 級的GalnAsN基極層和穿隧集極之DHBT的圖解。基極層係 分級成使得射極和集極接合之間在能帶間隙上有大約 40meV的能量差異。在基極和集極之間製出1〇〇人厚的穿隧 集極,其係由高能帶間隙材料In〇 5Ga〇 5p所組成。圖23顯 不圖22之DHBT的能帶間隙圖解。DHBT乃使用簡單的溼式 蝕刻法製成大面積元件(L=75vmx75vm),並且在共同的基 極和共同的射極架構中測試。圖24顯示其Gummel圖,而 圖25顯示圖22之DHBT的共同射極特徵。如圖24和託所 可以看到的,元件具有大約〇·12ν的低偏移電壓。 等效者 雖然已經參考較佳的具體態樣來特別顯示和描述本發 明,但是熟於此技藝者將理解到:在不偏離本發明由所附 申請專利範圍所包含的範圍之下,其中可以在型式和細節 上做出多種改變。 【圖式簡單說明】 (一)圖式部分 圖1圖解說明本發明之較佳具體態樣的InGaP / GalnAsN DHBT結構,其中X大約等於3y。 32 1288479 圖2是Gu匪el圖,其圖解說明對於本發明的InGaP/ GalnAsN DHBT 以及先前技藝的 InGaP/GaAs HBT 和 GaAs/ GaAs B JT而言,以打開電壓為函數的基極和集極電流。 圖3圖解說明對於本發明的InGaP/GalnAsN DHBT以 及先前技藝的InGaP / GaAs HBT和GaAs / GaAs BJT而言, 以基極片電阻為函數的打開電麗(當Jc = l. 78 A/cm2時)。 圖4圖解說明本發明的InGaP/ GalnAsN DHBT以及先 前技藝的InGaP/GaAs HBT兩者在名義基極厚度1 000A、 77QK下所測量的發光光譜。蝕刻移掉InGaAs和GaAs覆蓋 層而選擇性地終止於InGaP射極頂端之後才進行發光測量 。InGaP/GaAs HBT 和 InGaP/ GalnAsN DHBT 兩者之 η 型 GaAs集極的能帶間隙為1. 507eV。InGaP / GaAs HBT之ρ型 GaAs基極層的能帶間隙為1. 455eV,而InGaP / GalnAsN DHBT之ρ型GalnAsN基極層的能帶間隙為1. 408eV。 圖5圖解說明本發明的InGaP/ GalnAsN DHBT以及先 前技藝的InGaP / GaAs HBT兩者在名義基極厚度1500A下 的雙重晶體 X 光繞射(double crystal X-ray diffraction ,DCXRD)光譜。基極層尖峰的位置有標示出來。 圖6是Polaron C-V輪廓圖,其圖解說明越過本發明 的 InGaP/GalnAsN DHBT 以及先前技藝的 InGaP/GaAs HBT 中之基極層厚度的載子濃度。InGaP / GalnAsN DHBT以及 InGaP / GaAs HBT的名義基極厚度都是ΙΟΟΟΑ。選擇性地向 下#刻到基極層頂端之後才得到兩者的P〇 1 aron輪廓。 圖7A圖解說明較佳的InGaP / GalnAsN DHBT結構,其 33 1288479 在射極和基極之間有過渡層, 層和晶格匹配層。 而在集極和基極之間有過渡The third calculation (rb reduced by 11/3 and (re+rc) reduced to 1/2 of the baseline) approximates the use of thin and/or graded base structures and has improved component layout and size (to enable rb, Case under re and rc minimum Example 3 In order to improve amplifier efficiency and thus reduce operating voltage and extend battery life, it is desirable to reduce the offset voltage (VCE sat) and the skew voltage (Vk). One way to reduce the offset voltage is to minimize the asymmetry of the base/emitter and base/collector diodes for the turn-on voltage. Although the collector band gap 31 1288479 is wide, the DHBT has been shown to produce a potential barrier that results in a higher Vk and lowers the efficiency of the heterojunction. Low VCE, sat value, but in fact, this is because it is difficult to control the base/set insertion of a thin layer (penetrating collector) with high energy band gap, allowing simultaneous reduction of vCE, sat and vk, and improved components s efficiency. Figure 22 shows an illustration of a DHBT having a graded GalnAsN base layer and a tunneling collector. The base layer is graded such that there is an energy difference of approximately 40 meV across the band gap between the emitter and collector junctions. A 1 〇〇 thick tunneling collector is formed between the base and the collector, which is composed of a high energy band gap material In〇 5Ga〇 5p. Figure 23 shows an illustration of the band gap of the DHBT of Figure 22. DHBT is fabricated using a simple wet etch process for large area components (L = 75 vm x 75 vm) and tested in a common base and common emitter architecture. Figure 24 shows its Gummel diagram, while Figure 25 shows the common emitter feature of the DHBT of Figure 22. As can be seen in Figure 24 and the carrier, the component has a low offset voltage of approximately 〇12ν. The present invention has been particularly shown and described with reference to the preferred embodiments of the present invention, and it will be understood by those skilled in the art Make a variety of changes in style and detail. BRIEF DESCRIPTION OF THE DRAWINGS (I) Schematic Part FIG. 1 illustrates a preferred embodiment of the InGaP / GalnAsN DHBT structure in which X is approximately equal to 3 y. 32 1288479 FIG. 2 is a Gu匪el diagram illustrating base and collector currents as a function of turn-on voltage for the InGaP/ GalnAsN DHBT of the present invention and prior art InGaP/GaAs HBT and GaAs/GaAs B JT . Figure 3 illustrates the opening of the InGaP/GalnAsN DHBT of the present invention and the prior art InGaP / GaAs HBT and GaAs / GaAs BJT as a function of the base sheet resistance (when Jc = 1.78 A/cm2) ). Figure 4 illustrates the luminescence spectra measured for both the InGaP/ GalnAsN DHBT of the present invention and the prior art InGaP/GaAs HBT at nominal base thicknesses of 1 000 A, 77 QK. Luminescence measurements were taken after etching away the InGaAs and GaAs cap layers and selectively terminating at the InGaP emitter tip. The energy band gap of the n-type GaAs collector of the InGaP/GaAs HBT and the InGaP/ GalnAsN DHBT is 1.507 eV. The energy band gap of the p-type GalnAsN base layer of the InGaP / GaAs HBT is 1. 455 eV, and the band gap of the p-type GalnAsN base layer of the InGaP / Galn AsN DHBT is 1. 408 eV. Figure 5 illustrates a double crystal X-ray diffraction (DCXRD) spectrum of both the InGaP/ GalnAsN DHBT of the present invention and the prior art InGaP / GaAs HBT at a nominal base thickness of 1500A. The position of the base layer peak is indicated. Figure 6 is a Polaron C-V profile illustrating the carrier concentration of the base layer thickness in the InGaP/GalnAsN DHBT of the present invention and the prior art InGaP/GaAs HBT. The nominal base thickness of InGaP / GalnAsN DHBT and InGaP / GaAs HBT is ΙΟΟΟΑ. The P〇 1 aron profile of both is obtained by selectively engraving the top end of the base layer. Figure 7A illustrates a preferred InGaP / GalnAsN DHBT structure having 33 1288479 with a transition layer, a layer and a lattice matching layer between the emitter and the base. There is a transition between the collector and the base

圖解說明另外可以選擇的InGaP/GalnAsNGraphical description of additional InGaP/GalnAsN

圖7B和7C DHBT結構,其具有組成分級的基極層。 圖8是在固定不變之銦來源氣體流動速率下成長的摻Figures 7B and 7C DHBT structures having a base layer of compositional composition. Figure 8 is a blend of growth at a fixed indium source gas flow rate.

一一 ·人〜於、滩a秒動性果積而同時長出 摻雜奴之組成分級的GalnAsN基極層所需要之Tmif對四溴 化碳流動速率的圖形。 圖10是顯示InGaP / GalnAsN HBT的打開電壓要比 InGaP/ GaAs HBT來得低的圖形。 圖11是在固定不變之TMIF下成長的摻雜碳之 GalnAsN基極層中的△ Vbe對四溴化碳流動速率的圖形。 圖12是△ 乂“對TMIF的圖形。 圖13是用於範例2的實驗而具有組成分級之基極層的 DHBT結構。 圖14是用於範例2的實驗而具有固定組成之基極層的 DHBT結構。 圖15是Gummel圖,其比較具有固定組成之GalnAsN 基極層的DHBT和具有組成分級之GalnAsN基極層的DHBT。 圖16是比較具有固定組成之GalnAsN基極層的DHBT 和具有組成分級之GalnAsN基極層的DHBT,其DC電流增 盈以基極片電阻為函數的圖形。 1288479 圖17是Gummel圖,其比較具有組成分級之GalnAsN 基極層的DHBT和具有固定組成之GalnAsN基極層的兩個 DHBT。 圖18是比較具有組成分級之GalnAsN基極層的DHBT 和具有固定組成之GalnAsN基極層的兩個DHBT,其DC電 流增益以集極電流密度為函數的圖形。 圖19是比較具有固定組成之GalnAsN基極層的DHBT 和具有組成分級之GalnAsN基極層的DHBT,其外插電流增 益切斷頻率以集極電流密度為函數的圖形。 圖20是比較具有固定組成之GalnAsN基極層的DHBT 和具有組成分級之GalnAsN基極層的DHBT,其小訊號電流 增益以頻率為函數的圖形。 圖21是比較具有固定組成之GalnAsN基極層的DHBT 和具有組成分級之GalnAsN基極層的DHBT對於具有GaAs 基極層的傳統HBT而言,其尖峰f t以BVce。為函數的圖形 〇 圖22是顯示具有分級的GalnAsN基極層和穿隧集極之 DHBT的組成表。 圖23是圖22所述之DHBT的能帶間隙圖解。 圖24是圖22所述之DHBT的Gummel圖。 圖25顯示圖22所述之DHBT的共同射極特徵。 (二)元件代表符號 (無) 3511. The graph of the flow rate of Tmif to tetrabromocarbon required for the GalnAsN base layer of the composition of the doped slaves. Fig. 10 is a graph showing that the opening voltage of the InGaP / GalnAsN HBT is lower than that of the InGaP/GaAs HBT. Figure 11 is a graph of ΔVbe versus carbon tetrabromide flow rate in a carbon-doped GalnAsN base layer grown at a fixed TMIF. Figure 12 is a graph of Δ 乂 "for TMIF. Figure 13 is a DHBT structure having a compositionally graded base layer for the experiment of Example 2. Figure 14 is a base layer having a fixed composition for the experiment of Example 2. Figure 15 is a Gummel diagram comparing DHBT with a fixed composition of GalnAsN base layer and DHBT with a graded GalnAsN base layer. Figure 16 is a comparison of DHBT and composition with a fixed composition of GalnAsN base layer The DHBT of the graded GalnAsN base layer has a DC current gain as a function of the base sheet resistance. 1288479 Figure 17 is a Gummel plot comparing DHBT with a graded GalnAsN base layer and a GalnAsN base with a fixed composition Two DHBTs of the pole layer. Figure 18 is a graph comparing the DC current gain as a function of collector current density for a DHBT with a GalnAsN base layer composed of a graded structure and two DHBTs with a fixed composition of a GalnAsN base layer. 19 is a graph comparing a DHBT having a fixed composition of a GalnAsN base layer and a DHBT having a graded GalnAsN base layer, the extrapolation current gain cutoff frequency as a function of the collector current density. Comparing DHBT with a fixed composition of GalnAsN base layer and DHBT with a graded GalnAsN base layer, the small signal current gain is a function of frequency. Figure 21 is a comparison of DHBT with a fixed composition of GalnAsN base layer and DHBT with a graded GalnAsN base layer for a conventional HBT with a GaAs base layer, the peak ft of which is a function of BVce. Figure 22 shows a GalnAsN base layer with a gradation and a tunneling collector. Figure 23 is a diagram showing the band gap of the DHBT of Figure 22. Figure 24 is a Gummel diagram of the DHBT of Figure 22. Figure 25 shows the common emitter characteristics of the DHBT of Figure 22. ) Component symbol (none) 35

Claims (1)

imm 拾、申請專利範圍: u 一種異質接合雙極電晶體,其包括: (a) η型摻雜的集極; (b) 形成於集極上而包括ΠΙ—ν族材料的基極,其中 ΙίΙ V私材料包括銦和氮,其中基極乃摻雜以濃度為大約 Uxl〇19clr3到大約7.〇xl〇19cir3的碳,以及其中基極的組 成乃有所分級,以使銦和/或氮的濃度在基極一集極界面 處要尚於在基極一射極界面處,藉此基極的能帶間隙在基 極一集極界面處要比在基極—射極界面處低大約別社^到 大約120meV的範圍;以及 (c) 形成於基極上之η型摻雜的射極。 2·如申請專利範圍第1項的電晶體,其中基極包括 鎵、銦、砂和氮元素。 3·如申請專利範圍第2項的電晶體,其中集極是 GaAs ’射極是inGap、A1 InGaP或AlGaAs,並且此電晶體 是雙重異質接合雙極電晶體。 4·如申請專利範圍第1項的電晶體,其中基極層的 能帶間隙從基極層與集極接觸的表面到基極層與射極接觸 的表面呈線性地分級。 5·如申請專利範圍第4項的電晶體,其中分級基極 層的平均能帶間隙降低是比GaAs的能帶間隙少大約20meV 到大約300meV的範圍。 ___ 6·如申請專利範圍第5項的電晶體,其中分級基極 層的平均能帶間隙降低是比GaAs的能帶間隙少大約80meV 36 1288479 到大約30〇meV的範圍。 7·如申請專利範圍第5項的電晶體,其中分級基極 層的平均能帶間隙降低是比GaAs的能帶間隙少大約20meV 到大約200meV的範圍。 8·如申請專利範圍第3項的電晶體,其中基極層包 括化子式為Ga卜xInxAs卜yNy的一層,其中X和y分別獨立 地為大約1·〇χ1〇-4到大約2. 〇χ1(Γΐ。 9·如申請專利範圍第8項的電晶體,其中x大約等 於3y 〇 10·如申請專利範圍第8項的電晶體,其中X值在集 極處為大約〇· 2到大約〇·02的範圍,並且分級到射極處 之大約0.1到大約零的範圍,前提是χ在集極處要比在射 極處來得大。 11·如申請專利範圍第10項的電晶體,其中1在集 極處大約是〇·〇6,而在射極處大約是〇 〇1。 12·如申請專利範圍第9項的電晶體,其中基極層是 大約400Α到大約1500人厚,其片電阻為大約1〇〇Ω/平方 到大約400 Ω /平方。 13·如申請專利範圍第12項的電晶體,其中射極中 存在的η型摻雜物濃度範圍為大約3 5xl〇17cm—3到大約 4·5χ1〇ιγ„Γ3,並且集極中存在的n型摻雜物濃度範圍為大 約 9xl〇15CIir3 到大約 2xl〇16cnr3。 14.如申請專利範圍第13項的電晶體,其中射極和 集極乃摻雜以石夕。 37 1288479 15·如申請專利範圍第 大約500A到大約750A厚 約4500A厚。 14項的電晶體,其t射極是 並且集極是大約3500A到大 16.如申請專利範園第15項的電晶體,盆進一+勺 括配置於基極和集極之㈣第—過渡層,㈣—過渡2 有鄰接於基極之第一表面的第一表面,其中第一過渡層包 括選自由GaAs、InGaA〇 InGaAsN所構成之一群的: 摻雜材料。 ★ 17.如申請專利範圍第16項的電晶體,其進一步包 括第二過渡層,其具有鄰接於射極之第一表面的第一表面 和具有鄰接於基極之第二表面的第二表面,其二過渡 層包括選自由GaAs、InGaAs和InGaAsN所構成之一群的n 型摻雜材料。 18·如申請專利範圍第17項的電晶體,其進一步包 括晶格匹配層,其具有鄰接於集極之第一表面的第一表面 和具有鄰接於第一過渡層之第二表面的第二表面,其中晶 格匹配層是寬能帶間隙的材料。 ΘΒ 19·如申請專利範圍第18項的電晶體,其中晶格匹 配層是選自由InGaP、AlInGaP和A1GaAs所構成的一群。 20.如申請專利範圍第17項的電晶體,其中第一和 第二過渡層是大約40A到大約60A厚。 21·如申請專利範圍第18項的電晶體,其中第一和 第二過渡層是大約40A到大約60A厚,並且晶格匹配層是 大約150A到大約250A厚。 38 1288479 22· 一種製造異質接合雙極電晶體的方法,其包括 列步驟: 八匕 (a) 在η型摻雜的GaAs集極層上由鎵、銦、砷和氮 來源長出包括鎵,、砷和氮的基極層,其中基極層由外 部碳來源而p型掺雜以碳,碳摻雜濃度為大約i 5xi〇i9cm_ 3到大約7· 〇χ1〇ΐ9⑶-3,以及其中基極的組成乃有所分級 以使銦和/或氮的濃度在基極—集極界面處要高於在基極 —射極界面處,藉此基極的能帶間隙在基極—集極界面處 要比在基極一射極界面處低大約2〇mev到大約12〇meV的 範圍,以及 (b) 在基極層上長出η型摻雜的射極層。 23·如申請專利範園第22項的方法,其中外部碳來 源是四溴化碳或四氣化碳。 24.如申請專利範圍第23項的方法,其中鎵來源是 選自三甲基錁和三乙基錁。 25·如申請專利範圍第24項的方法,其中氮來源是 氨、二甲基聯氨或三級丁基胺。 26·如申請專利範圍第25項的方法,其中砰來源對 鎵來源的比例是大約2. 0到大約3. 5。 27·如申請專利範圍第26項的方法,其中基極是在 低於大約750°C的溫度下成長。 28·如申請專利範圍第27項的方法,其中基極是在 大約500°C到大約600°C的溫度下成長。 29·如申請專利範圍第27項的方法,其中基極層包 39 1288479 為GaixiMsi-yNy的一層,其中χ和y分別獨立 地為大約i.Oxio-4到大約2.0x10-。 30. 如申請專利範圍第29項的方法其中1大 於3y 〇 31. 如申請專利範圍帛29項的方法,其中集極包括 ^ ’射極包括選自由1_、AlInGaP和A1GaAs所構成 之群的材料,並且其中此電晶體是雙重異質接合雙極電 晶體。 、如申叫專利範圍第29項的方法,其在長出基極 層之前進-步包括於集極層上長& n型摻雜之第一過渡層 的步驟,其中基極層是長在η型掺雜的第一過渡層上,並 且第-過渡層具有小於集極能帶間隙的分級能帶間隙或能 帶間隙。 33·如申明專利範圍第32項的方法,其中第一過渡 層是選自由GaAs、InGaAs和InGaAsN所構成的一群。 34·如申請專利範圍第33項的方法,其在長出11型 摻雜的射極層之前進一步包括於基極上長出第二過渡層的 步驟,其中第二過渡層具有鄰接於基極表面的第一表面和 具有鄰接於射極表面的第二表面,並且第二過渡層的摻雜 漠度要比射極的摻雜濃度低至少一個數量級。 35·如申請專利範圍第34項的方法,其中第二過渡 層疋選自由GaAs、InGaAs和InGaAsN所構成的一群。 36·如申請專利範圍第35項的方法,其中所形成的 第一過渡層、第二過渡層、或者第一過渡層和第二過渡層 40 1288479 兩者具有摻雜突峰。 37.如申請專利範圍第35項的方法,其在長出n型 捧雜的第-過渡層之前進一步包括於集極上長出晶格匹配 層的步驟,其中晶格匹配層具有鄰接於集極之第一表面的 第一表面和具有鄰接於第一過渡層之第二表面的第二表面。 38·如申請專利範圍第37項的方法,其中晶格匹配 層包括InGaP。 39· 種形成分級之半導體層的方法,此分級的半導 體層從第-表面經過該層到第二表面具有基本上線性分級 的能帶間隙以及基本上固定不變之摻雜x移動性的乘積, 此方法包括以下步驟·· (a) 比較多個校正層的摻雜X移動性的乘積,其中每 一層係在沉積週期表之ΙΠ或V族原子的有機金屬合物 或者沉積碳的四齒化碳化合物當中任一者之明確區分的流 動速率下所形成,藉此決定形成基本上固定不變的摻雜x 移動|·生乘積所需要之有機金屬化合物和四自化碳的相對流 動速率;以及 (b) 在該相對流動速率下,將有機金屬化合物和四南 化碳化合物流動於一表面上,以形成基本上固定不變之摻 雜X移動性的乘積,而在沉積期間改變該流動速率,藉此 形成在整個分級之半導體層中基本上呈線性分級的能帶間 隙。 40.如申請專利範圍第39項的方法,其進一步包括 於接合το件的製造期間在第二半導體層上沉積該分級層的 步驟。 1288479 41 ·如申請專利範圍第 體層是集極層。 42·如申請專利範圍第 體層是射極層。 40項的方法,其中第二半導 40項的方法,其中第二半導 43. 如申請專利範圍帛39帛的方法,其中分級的半 導體層包括鎵、銦和坤’並且決定㈣化破的沉積速率以 形成基本上固定不變之摻雜x移動性乘積的有機金屬化合 物包括有機銦化合物。 σ 44. 如申請專利範圍f 43項的方法其中四齒化碳 45. 如申請專利範圍帛44㈣方法其 化合物進一步包括氮來源氣體。 屬 46. 如申請專利範圍帛4〇項的方法其中沉積了分 級之半導體層的第二半導體層包括GaAs。 47. 如申請專利範圍帛46㈣方法,其進一步包括 在分級之半導體層上沉積第三半導體層的步驟。 47項的方法,其中第三半導 48·如申請專利範圍第 體層是InGaP。 49.如申請專利範圍帛46項的方法其中每一校正 層的摻雜X移動性乘積乃關聯於能帶間隙,藉此在分級層 :第-和第二表面處的能帶間隙配合了摻雜χ移動心 ,將會校正於沉積該分級半導體層所需要之有機金屬化 3物和四鹵化碳的相對流動速率。 5〇·如申請專利範圍帛49㈣方法,其令該能帶間 42 1288479 隙乃相對於GaAs而校正成為使用該校正層做為基極層之 接合元件的基極一射極電壓。 51·如申凊專利範圍第50項的方法,其中所形成的 、及半導體層疋異質接合雙極電晶體中的基極層。 ,”請專利麵51,的方法,其曰中有機金屬 ^物和θ齒化碳的流動速率造成所得之分級 ▼間隙從該異質接合雙極電晶體的基極土 、月b /集極接合降低。 /射極接合往基極 拾壹、囷式: 如次頁。 43Imm pick, patent scope: u A heterojunction bipolar transistor comprising: (a) an n-type doped collector; (b) a base formed on the collector and comprising a ΠΙ-ν family material, wherein ΙίΙ V private material includes indium and nitrogen, wherein the base is doped with carbon at a concentration of about Uxl 〇 19clr3 to about 7. 〇 xl 〇 19cir3, and wherein the composition of the base is graded to make indium and/or nitrogen The concentration at the base-collector interface is still at the base-emitter interface, whereby the base band gap is lower at the base-collector interface than at the base-emitter interface. a range of approximately 120 meV; and (c) an n-type doped emitter formed on the base. 2. A transistor as claimed in claim 1, wherein the base comprises gallium, indium, sand and nitrogen. 3. A transistor as claimed in claim 2, wherein the collector is GaAs' emitter is inGap, A1 InGaP or AlGaAs, and the transistor is a double heterojunction bipolar transistor. 4. The transistor of claim 1, wherein the energy band gap of the base layer is linearly graded from a surface where the base layer contacts the collector to a surface where the base layer contacts the emitter. 5. The transistor of claim 4, wherein the average band gap reduction of the graded base layer is less than about 20 meV to about 300 meV less than the band gap of the GaAs. ___ 6. The transistor of claim 5, wherein the average band gap reduction of the graded base layer is about 80 meV 36 1288479 to about 30 〇 meV less than the energy band gap of GaAs. 7. The transistor of claim 5, wherein the average band gap reduction of the graded base layer is less than about 20 meV to about 200 meV less than the band gap of the GaAs. 8. The transistor of claim 3, wherein the base layer comprises a layer of the formula GabxInxAsb yNy, wherein X and y are each independently from about 1·〇χ1〇-4 to about 2. 〇χ1 (Γΐ. 9. The transistor of claim 8 of the patent application, wherein x is approximately equal to 3y 〇10. The transistor of claim 8 of the patent scope, wherein the X value is approximately 〇·2 at the collector A range of approximately 〇·02, and is graded to the range of approximately 0.1 to approximately zero at the emitter, provided that χ is greater at the collector than at the emitter. 11·Calculator as in claim 10 Wherein 1 is approximately 〇·〇6 at the collector and approximately 〇〇1 at the emitter. 12· The transistor of claim 9 wherein the base layer is approximately 400 Α to approximately 1500 厚The sheet resistance is about 1 〇〇Ω/square to about 400 Ω/square. 13. The transistor of claim 12, wherein the concentration of the n-type dopant present in the emitter ranges from about 3 5 x 1 〇 17cm-3 to about 4·5χ1〇ιγ„Γ3, and the concentration range of n-type dopants present in the collector is large 9xl〇15CIir3 to about 2xl〇16cnr3. 14. The transistor of claim 13, wherein the emitter and the collector are doped with Shi Xi. 37 1288479 15 · If the patent application range is about 500A to about 750A thick Approximately 4500A thick. The 14-item transistor has a t-emitter and a collector of about 3500A to a maximum of 16. As in the patent of the 15th patent, the basin is filled with a + spoon and is disposed at the base and collector. (4) a first-transition layer, (four)-transition 2 having a first surface adjacent to the first surface of the base, wherein the first transition layer comprises a group selected from the group consisting of GaAs, InGaA〇InGaAsN: doped material. The transistor of claim 16, further comprising a second transition layer having a first surface adjacent to the first surface of the emitter and a second surface having a second surface adjacent to the base, The transition layer includes an n-type dopant material selected from the group consisting of GaAs, InGaAs, and InGaAsN. 18. The transistor of claim 17, further comprising a lattice matching layer having a layer adjacent to the collector a surface a surface and a second surface having a second surface adjacent to the first transition layer, wherein the lattice matching layer is a material having a wide band gap. ΘΒ 19. The transistor of claim 18, wherein the lattice matching layer A group selected from the group consisting of InGaP, AlInGaP, and A1 GaAs. 20. The transistor of claim 17, wherein the first and second transition layers are from about 40 A to about 60 A thick. The transistor of the item, wherein the first and second transition layers are about 40A to about 60A thick, and the lattice matching layer is about 150A to about 250A thick. 38 1288479 22· A method of fabricating a heterojunction bipolar transistor comprising the steps of: erbium (a) growing gallium, indium, arsenic and nitrogen sources on a n-doped GaAs collector layer, including gallium, a base layer of arsenic and nitrogen, wherein the base layer is made of an external carbon source and p-type doped with carbon, and the carbon doping concentration is about i 5xi〇i9cm_ 3 to about 7·〇χ1〇ΐ9(3)-3, and a base thereof The composition of the poles is graded such that the concentration of indium and/or nitrogen is higher at the base-collector interface than at the base-emitter interface, whereby the energy band gap of the base is at the base-collector The interface is at a range of about 2 〇 meV to about 12 〇 meV lower than at the base-emitter interface, and (b) an n-type doped emitter layer is grown on the base layer. 23. For example, the method of applying for patent paradigm 22, wherein the external carbon source is carbon tetrabromide or carbon tetrahydrate. 24. The method of claim 23, wherein the source of gallium is selected from the group consisting of trimethyl hydrazine and triethyl hydrazine. 25. The method of claim 24, wherein the source of nitrogen is ammonia, dimethyl hydrazine or tertiary butylamine. The ratio of the source of the source of the gallium is from about 2.0 to about 3.5. 27. The method of claim 26, wherein the base is grown at a temperature below about 750 °C. 28. The method of claim 27, wherein the base is grown at a temperature of from about 500 ° C to about 600 ° C. 29. The method of claim 27, wherein the base layer package 39 1288479 is a layer of GaixiMsi-yNy, wherein χ and y are independently from about i.Oxio-4 to about 2.0x10-, respectively. 30. The method of claim 29, wherein 1 is greater than 3y 〇 31. The method of claim 29, wherein the collector comprises: ^ the emitter comprises a material selected from the group consisting of 1_, AlInGaP, and A1GaAs. And wherein the transistor is a double heterojunction bipolar transistor. The method of claim 29, wherein the step of stepping in the first layer of the n-doped first transition layer on the collector layer before the base layer is grown, wherein the base layer is long On the n-type doped first transition layer, and the first-transition layer has a graded energy band gap or band gap smaller than the collector band gap. 33. The method of claim 32, wherein the first transition layer is selected from the group consisting of GaAs, InGaAs, and InGaAsN. 34. The method of claim 33, further comprising the step of growing a second transition layer on the base prior to growing the 11-doped emitter layer, wherein the second transition layer has a surface adjacent to the base The first surface and the second surface adjacent to the surface of the emitter, and the doping inversion of the second transition layer is at least one order of magnitude lower than the doping concentration of the emitter. 35. The method of claim 34, wherein the second transition layer is selected from the group consisting of GaAs, InGaAs, and InGaAsN. 36. The method of claim 35, wherein the first transition layer, the second transition layer, or both the first transition layer and the second transition layer 40 1288479 have doped peaks. 37. The method of claim 35, further comprising the step of growing a lattice matching layer on the collector before growing the n-type transition layer, wherein the lattice matching layer has a contiguous collector a first surface of the first surface and a second surface having a second surface adjacent to the first transition layer. 38. The method of claim 37, wherein the lattice matching layer comprises InGaP. 39. A method of forming a graded semiconductor layer, the graded semiconductor layer having a substantially linearly graded energy band gap from the first surface through the layer to the second surface and a substantially constant product of doping x mobility The method comprises the following steps: (a) Comparing the product of the doping X mobility of a plurality of correction layers, wherein each layer is an organometallic compound of a group or group V atom or a tetradentate of carbon deposited in a deposition period table. Formed at a clearly differentiated flow rate of any of the carbon compounds, thereby determining the relative flow rates of the organometallic compounds and tetra-self-carbons required to form a substantially constant doping x-movement product. And (b) flowing the organometallic compound and the tetra-n-carbon compound on a surface at the relative flow rate to form a product of substantially constant doping X mobility, which is changed during deposition The flow rate, thereby forming a substantially linear band gap in the entire graded semiconductor layer. 40. The method of claim 39, further comprising the step of depositing the graded layer on the second semiconductor layer during fabrication of the bond. 1288479 41 • As claimed in the patent area, the body layer is the collector layer. 42. If the scope of the patent application is the emitter layer. The method of item 40, wherein the second half of the method of 40, wherein the second half is 43. The method of claim 帛 39帛, wherein the graded semiconductor layer comprises gallium, indium, and kun' and determines (four) The organometallic compound having a deposition rate to form a substantially constant doping x mobility product includes an organic indium compound. σ 44. The method of claim 41, wherein the tetradentate carbon 45. The method of claim 44 (4), wherein the compound further comprises a nitrogen source gas. The method of claim 46, wherein the second semiconductor layer on which the graded semiconductor layer is deposited comprises GaAs. 47. The method of claim 46, wherein the method further comprises the step of depositing a third semiconductor layer on the graded semiconductor layer. The method of item 47, wherein the third half is 48. The body layer of the patent application is InGaP. 49. The method of claim 46, wherein the doping X mobility product of each of the correction layers is associated with an energy band gap, whereby the band gaps at the first and second surfaces are combined with the band gap The dopant movement center will correct the relative flow rate of the organometallic 3 and tetrahalide carbon required to deposit the graded semiconductor layer. 5. The method of claim 49 (4) is such that the gap between the energy bands 42 1288479 is corrected relative to GaAs to the base-emitter voltage of the bonding element using the correction layer as the base layer. The method of claim 50, wherein the formed and the semiconductor layer are heterogeneously bonded to the base layer in the bipolar transistor. ," the method of Patent No. 51, the flow rate of the organometallics and the θ-toothed carbon in the crucible causes the resulting fractional ▼ gap from the base soil of the heterojunction bipolar transistor, and the monthly b/collar junction Reduced. /The emitter is connected to the base and the 囷: as the next page.
TW92107363A 2002-04-05 2003-04-01 Bipolar transistor with graded base layer TWI288479B (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US37075802P 2002-04-05 2002-04-05
US37164802P 2002-04-10 2002-04-10
US10/121,444 US6847060B2 (en) 2000-11-27 2002-04-10 Bipolar transistor with graded base layer

Publications (2)

Publication Number Publication Date
TW200308088A TW200308088A (en) 2003-12-16
TWI288479B true TWI288479B (en) 2007-10-11

Family

ID=34108673

Family Applications (1)

Application Number Title Priority Date Filing Date
TW92107363A TWI288479B (en) 2002-04-05 2003-04-01 Bipolar transistor with graded base layer

Country Status (4)

Country Link
JP (1) JP2005522883A (en)
CN (1) CN100448024C (en)
AU (1) AU2003223423A1 (en)
TW (1) TWI288479B (en)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2013001676A1 (en) * 2011-06-30 2013-01-03 パナソニック株式会社 Thin film transistor device and method for producing thin film transistor device
CN103137666B (en) * 2011-11-23 2015-12-09 上海华虹宏力半导体制造有限公司 A kind of longitudinal P NP bipolar transistor and manufacture method thereof
CN105051873B (en) 2013-03-19 2017-06-13 株式会社村田制作所 Heterojunction bipolar transistor
CN103545398B (en) * 2013-10-16 2016-06-08 北京工业大学 The double-heterojunctiophototransistor phototransistor detector of the unidirectional carrier transport of base district gradual change
CN104900689B (en) * 2015-06-08 2019-05-17 中国科学院半导体研究所 Reduce the GaN base HBT epitaxial structure and growing method of base resistance rate
CN106653826B (en) * 2016-12-26 2019-01-08 厦门市三安集成电路有限公司 A kind of compound semiconductor heterojunction bipolar transistor
CN110649088A (en) * 2019-09-30 2020-01-03 厦门市三安集成电路有限公司 Epitaxial structure and low turn-on voltage transistors
CN114859200B (en) * 2022-04-28 2024-04-12 西安唐晶量子科技有限公司 Method for evaluating material characteristics of base layer of InGaP/GaAs HBT epitaxial wafer
CN116344585A (en) * 2023-03-29 2023-06-27 绍兴中芯集成电路制造股份有限公司 Heterojunction bipolar transistor and method of manufacturing the same
CN117116763B (en) * 2023-10-25 2024-01-23 新磊半导体科技(苏州)股份有限公司 Molecular beam epitaxial growth method of carbon doped HBT device
CN117766389B (en) * 2023-12-26 2025-07-04 全磊光电股份有限公司 Heterojunction bipolar transistor and MOCVD epitaxial growth method thereof

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2000133654A (en) * 1998-10-23 2000-05-12 Furukawa Electric Co Ltd:The Manufacturing method of bipolar transistor
JP2000223497A (en) * 1999-01-28 2000-08-11 Furukawa Electric Co Ltd:The Heterojunction bipolar transistor and manufacturing method thereof
FR2795871B1 (en) * 1999-07-01 2001-09-14 Picogiga Sa HETEROJUNCTION TRANSISTOR III-V, IN PARTICULAR HEMT FIELD-EFFECT TRANSISTOR OR BIPOLAR HETEROJUNCTION TRANSISTOR
CN1111313C (en) * 1999-07-02 2003-06-11 北京工业大学 Bipolar heterojunction transistor

Also Published As

Publication number Publication date
CN100448024C (en) 2008-12-31
AU2003223423A1 (en) 2003-10-27
TW200308088A (en) 2003-12-16
CN1647281A (en) 2005-07-27
JP2005522883A (en) 2005-07-28

Similar Documents

Publication Publication Date Title
US6847060B2 (en) Bipolar transistor with graded base layer
US7186624B2 (en) Bipolar transistor with lattice matched base layer
King et al. Si/Si/sub 1-x/Ge/sub x/heterojunction bipolar transistors produced by limited reaction processing
Patton et al. 75-GHz f/sub T/SiGe-base heterojunction bipolar transistors
EP0541971B1 (en) A graded bandgap single-crystal emitter heterojunction bipolar transistor
US7345327B2 (en) Bipolar transistor
US6756615B2 (en) Heterojunction bipolar transistor and its manufacturing method
US6765242B1 (en) Npn double heterostructure bipolar transistor with ingaasn base region
TWI288479B (en) Bipolar transistor with graded base layer
JP2804095B2 (en) Heterojunction bipolar transistor
Sturm et al. Graded-base Si/Si/sub 1-x/Ge/sub x//Si heterojunction bipolar transistors grown by rapid thermal chemical vapor deposition with near-ideal electrical characteristics
Welser et al. Role of neutral base recombination in high gain AlGaAs/GaAs HBT's
Oka et al. Low turn-on voltage GaAs heterojunction bipolar transistors with a pseudomorphic GaAsSb base
JP3515944B2 (en) Hetero bipolar transistor
Willén et al. High-gain, high-speed InP/InGaAs double-heterojunction bipolar transistors with a step-graded base-collector heterojunction
Liu et al. High-performance InP/GaAsSb/InP DHBTs grown by MOCVD on 100 mm InP substrates using PH3 and AsH3
Slater et al. Low emitter resistance GaAs based HBT's without InGaAs caps
US7019340B2 (en) Bipolar transistor device and method for fabricating the same
US6744078B2 (en) Heterojunction structure with a charge compensation layer formed between two group III-V semiconductor layers
US6800879B2 (en) Method of preparing indium phosphide heterojunction bipolar transistors
Roenker Reliability issues for III-V heterojunction bipolar transistors
JP3326378B2 (en) Semiconductor device
KR101082773B1 (en) Compound semiconductor device and its manufacturing method
JP2557613B2 (en) Heterojunction bipolar transistor
Beam III et al. Gas-source molecular beam epitaxy of electronic devices

Legal Events

Date Code Title Description
MK4A Expiration of patent term of an invention patent