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TWM667354U - Plasma erosion resistant device structure - Google Patents

Plasma erosion resistant device structure Download PDF

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Publication number
TWM667354U
TWM667354U TW113212130U TW113212130U TWM667354U TW M667354 U TWM667354 U TW M667354U TW 113212130 U TW113212130 U TW 113212130U TW 113212130 U TW113212130 U TW 113212130U TW M667354 U TWM667354 U TW M667354U
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Taiwan
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plasma
coating
layer
erosion resistant
surface modification
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TW113212130U
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Chinese (zh)
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吳宗豐
林佳德
邱國揚
陳柏翰
黃柏嘉
林志華
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翔名科技股份有限公司
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Priority to TW113212130U priority Critical patent/TWM667354U/en
Publication of TWM667354U publication Critical patent/TWM667354U/en

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Abstract

一種抗電漿侵蝕元件結構,特別是用於半導體製程之相關設備或設施的元件。該元件結構包括多層結構,包括由不鏽鋼合金、鋁合金、高分子或陶瓷材料製成的基材;一層由金屬氧化物、氟化物或氮化物構成的表面塗層,該塗層通過等離子噴塗、氣溶膠噴塗、物理氣相沉積、原子層沉積或電漿增強化學氣相沉積技術沉積而成;以及通過使用惰性氣體進行離子轟擊,使該塗層進一步緻密化的表面改質層。此多層結構大幅提升了元件表面之硬度、密度及耐磨性,增強了抗電漿侵蝕的能力,並有效減少因塗層剝落而產生的粉塵。本新型不僅提升了元件的耐用性,還有效降低了製程中的顆粒污染,滿足了先進半導體製造中的嚴苛需求。。A plasma erosion resistant component structure, in particular a component used in semiconductor process related equipment or facilities. The component structure comprises a multi-layer structure, including a substrate made of stainless steel alloy, aluminum alloy, polymer or ceramic material; a surface coating layer composed of metal oxide, fluoride or nitride, which is deposited by plasma spraying, aerosol spraying, physical vapor deposition, atomic layer deposition or plasma enhanced chemical vapor deposition technology; and a surface modification layer that further densifies the coating layer by ion bombardment using an inert gas. This multi-layer structure greatly improves the hardness, density and wear resistance of the component surface, enhances the ability to resist plasma erosion, and effectively reduces the dust generated by coating peeling. This new type not only improves the durability of the component, but also effectively reduces the particle contamination in the process, meeting the stringent requirements of advanced semiconductor manufacturing.

Description

抗電漿侵蝕元件結構Plasma erosion resistant device structure

本新型一般涉及用於半導體製程設備中的元件,特別是解決抗電漿侵蝕的問題。更具體地說,本新型涉及腔體內部元件的結構設計及材料組成,以增強耐用性並減少在先進半導體製程中可能產生的污染。The present invention generally relates to components used in semiconductor process equipment, and more particularly to solving the problem of plasma erosion resistance. More specifically, the present invention relates to the structural design and material composition of components inside the chamber to enhance durability and reduce possible contamination in advanced semiconductor processes.

在半導體產業中,基於電漿的製程對於各種製造步驟相當重要,包括蝕刻、沉積及表面改質。電漿被應用於專門的製程腔體中,以實現微觀層級且精確的材料去除與沉積,從而製造出複雜的半導體裝置。 腔體內部元件,如電極、襯墊和氣體分配板,持續暴露於反應性電漿環境中。為了承受這些苛刻的條件,這些元件傳統上採用金屬(如不鏽鋼)或石英材料製造。然而,隨著半導體裝置越來越複雜,製程能力不斷提升,對腔體元件的要求變得更加嚴苛,需進行表面處理以確保元件的使用壽命和製程可靠性。 為減少電漿引起的劣化,業界發展了在腔體元件上進行表面微結構處理或塗層的技術。這些表面改質技術旨在賦予元件抗電漿腐蝕性能,從而降低基材剝落的速率並減少顆粒污染的生成,這些污染可能導致半導體基材中的缺陷。常用的表面處理技術包括物理氣相沉積、化學氣相沉積及各種電漿噴塗方法。 儘管已有這些技術進展,問題仍然存在。傳統材料如金屬和石英天生具有限的抗電漿侵蝕能力,導致磨損加劇並最終導致表面處理層的剝落。這些塗層的脫落不僅破壞了腔體元件的完整性,還會在製程環境中引入粉塵顆粒,對產品質量和良率產生不利影響。 作為金屬和石英基材的替代方案,燒結陶瓷材料因其優異的抗電漿腐蝕性被廣泛探索。像氧化鋁(Al₂O₃)、碳化矽(SiC)和二氧化鋯(ZrO₂)等陶瓷材料在電漿環境中具有更好的耐用性。然而,燒結陶瓷也存在一些限制。燒結陶瓷基材的天然多孔性可能會吸附污染物,從而降低腔體內環境的純度。此外,燒結過程往往會在陶瓷表面留下黏著劑殘留,進一步降低其抗腐蝕性,並影響腔體元件的性能。 因此,迫切需要一種創新的元件結構,不僅能抵抗電漿引起的侵蝕,還能將顆粒污染的生成降至最低。該結構應具有高硬度、高密度及耐磨耗性,並具備良好的保護塗層附著力,以確保元件的長壽命並維持半導體製程環境的純度。 In the semiconductor industry, plasma-based processes are important for various manufacturing steps, including etching, deposition, and surface modification. Plasma is applied in specialized process chambers to achieve microscopic and precise material removal and deposition to create complex semiconductor devices. Chamber internal components, such as electrodes, pads, and gas distribution plates, are continuously exposed to the reactive plasma environment. To withstand these harsh conditions, these components are traditionally made of metal (such as stainless steel) or quartz materials. However, as semiconductor devices become more complex and process capabilities continue to increase, the requirements for chamber components become more stringent, requiring surface treatment to ensure component life and process reliability. To reduce plasma-induced degradation, the industry has developed techniques for surface microstructuring or coating on cavity components. These surface modification techniques are intended to render the components resistant to plasma corrosion, thereby reducing the rate of substrate peeling and reducing the generation of particle contamination that can cause defects in the semiconductor substrate. Common surface treatment techniques include physical vapor deposition, chemical vapor deposition, and various plasma spraying methods. Despite these technological advances, problems remain. Traditional materials such as metals and quartz inherently have limited resistance to plasma attack, resulting in increased wear and ultimately peeling of the surface treatment layer. The detachment of these coatings not only destroys the integrity of the chamber components, but also introduces dust particles into the process environment, which has an adverse effect on product quality and yield. As an alternative to metal and quartz substrates, sintered ceramic materials have been widely explored due to their excellent resistance to plasma corrosion. Ceramic materials such as alumina (Al₂O₃), silicon carbide (SiC), and zirconium dioxide (ZrO₂) have better durability in plasma environments. However, sintered ceramics also have some limitations. The natural porosity of sintered ceramic substrates may absorb contaminants, thereby reducing the purity of the environment within the chamber. In addition, the sintering process often leaves adhesive residues on the ceramic surface, further reducing its corrosion resistance and affecting the performance of the cavity components. Therefore, there is an urgent need for an innovative component structure that can not only resist plasma-induced corrosion but also minimize the generation of particle contamination. The structure should have high hardness, high density and wear resistance, and have good adhesion of the protective coating to ensure the long life of the component and maintain the purity of the semiconductor process environment.

本新型提供一種設計用於半導體製程設備的抗電漿侵蝕元件結構。此創新結構針對在嚴苛電漿環境中增強耐用性並減少污染的關鍵需求進行了改善。 本新型的抗電漿侵蝕元件結構包括一基材、塗覆於基材之一上表面之一塗層、與一表面改質層。其中,基材作為基礎層,其材質可為金屬、高分子或陶瓷材料。其中,金屬包括不鏽鋼類型如SUS304和SUS316、各類鋁合金(例如5000系列、6000系列、7000系列);高分子材料例如環氧樹脂、聚氯乙烯等;陶瓷材料例如為氧化鋁、氮化鋁(AlN)、二氧化矽(SiO₂)、碳化矽(SiC)、氮化矽(SiN)、二氧化鋯(ZrO₂)和矽(Si)等陶瓷基材。 此外,塗層是直接設置於基材至少一上表面,該塗層旨在增強硬度、耐磨性及抗腐蝕性。塗層材料包括金屬氧化物、氟化物及氮化物,包括但不限於二氧化鈦(TiO₂)、氧化鋁(Al₂O₃)、氟化釔(YF₃)、氧化鉺(Er₂O₃)、氧化釓(Gd₂O₃)、氧化釔(Y₂O₃)、氧氟化釔(YOF)、釔鋁石榴石(YAG)、釔鋁單氧化物(YAM)、鉺鋁石榴石(EAG)及其混合物。所述塗層通過沉積技術沉積於基材之一上表面,所述沉積技術包括大氣等離子噴塗(atmospheric plasma spraying, APS)、懸浮等離子噴塗(suspension plasma spraying, SPS)、真空等離子噴塗(vacuum plasma spraying, VPS)、氣溶膠噴塗(aerosol deposition, ADM)、物理氣相沉積(physical vapor deposition, PVD)、原子層沉積(atomic layer deposition, ALD)或電漿增強化學氣相沉積(plasma-enhanced chemical vapor deposition, PECVD),塗層厚度範圍為0.1 µm至250 µm,硬度範圍為400 HV至1500 HV。表面改質層是經過離子轟擊進行處理,使其表面孔隙率至少較該塗層降低50%以上。此離子轟擊過程是使用惰性氣體如氬氣、氪氣、氙氣或氡氣,在100–3000 mA的電流、100–1500 V的電壓、5–500 sccm的氣體流量及1.0E-1至1.0E-6 Torr的操作壓力的控制條件下進行。離子轟擊過程增強了塗層的抗電漿侵蝕性、附著力及耐磨性,從而有效減少因塗層剝落引起的粉塵生成,並延長元件的使用壽命。 本新型的主要優點包括: 增強的抗電漿侵蝕性:高密度表面改質層與強韌的表面塗層的組合提供了優異的抗電漿侵蝕性,確保元件在苛刻的半導體製程環境中保持持續穩定的性能。 減少顆粒污染:通過減少塗層剝落與基材劣化,本新型顯著降低了粉塵顆粒的生成,從而提升了半導體製造過程中的產品質量和良率。 材料的多樣性與彈性:本新型可使用多種基材材料及多種沉積技術,提供了針對特定應用需求和製程條件的定制化選擇。 改良的機械性能:多層結構提供了高硬度、高密度及耐磨性,這些特性共同促進了腔體內部元件的耐用性與可靠性。 簡化的製造過程:使用先進的沉積技術及離子轟擊進行表面改質,簡化了高純度抗侵蝕元件的生產,克服了傳統燒結陶瓷與金屬基元件的限制。 總而言之,本新型提供了一種針對半導體製程設備所面臨的挑戰的創新解決方案。透過結合強韌的基材與專業設計的表面塗層及表面改質層,本新型實現了增強的耐用性、減少污染及改良的整體性能,滿足了日益增長的先進半導體製造技術的需求。 為讓本新型之上述特徵和優點能更明顯易懂,下文特舉較佳實施例,並配合所附圖式,作詳細說明如下。 The present invention provides a plasma erosion resistant component structure designed for semiconductor process equipment. This innovative structure improves the key requirements of enhancing durability and reducing pollution in harsh plasma environments. The plasma erosion resistant component structure of the present invention includes a substrate, a coating layer coated on an upper surface of the substrate, and a surface modification layer. The substrate is used as a base layer, and its material can be metal, polymer or ceramic material. Among them, metals include stainless steel types such as SUS304 and SUS316, various aluminum alloys (such as 5000 series, 6000 series, 7000 series); polymer materials such as epoxy resin, polyvinyl chloride, etc.; ceramic materials such as alumina, aluminum nitride (AlN), silicon dioxide (SiO₂), silicon carbide (SiC), silicon nitride (SiN), zirconium dioxide (ZrO₂) and silicon (Si) ceramic substrates. In addition, the coating is directly disposed on at least one upper surface of the substrate, and the coating is intended to enhance hardness, wear resistance and corrosion resistance. Coating materials include metal oxides, fluorides and nitrides, including but not limited to titanium dioxide (TiO₂), aluminum oxide (Al₂O₃), yttrium fluoride (YF₃), gerahertz oxide (Er₂O₃), gadolinium oxide (Gd₂O₃), yttrium oxide (Y₂O₃), yttrium oxyfluoride (YOF), yttrium aluminum garnet (YAG), yttrium aluminum monoxide (YAM), erbium aluminum garnet (EAG) and mixtures thereof. The coating is deposited on one of the upper surfaces of the substrate by a deposition technique, wherein the deposition technique includes atmospheric plasma spraying (APS), suspension plasma spraying (SPS), vacuum plasma spraying (VPS), aerosol deposition (ADM), physical vapor deposition (PVD), atomic layer deposition (ALD) or plasma-enhanced chemical vapor deposition (PECVD), and the coating thickness ranges from 0.1 µm to 250 µm and the hardness ranges from 400 HV to 1500 HV. The surface modification layer is treated by ion bombardment to reduce the surface porosity by at least 50% compared to the coating. The ion bombardment process is carried out using an inert gas such as argon, krypton, xenon or radon, under the controlled conditions of 100–3000 mA current, 100–1500 V voltage, 5–500 sccm gas flow and 1.0E-1 to 1.0E-6 Torr operating pressure. The ion bombardment process enhances the plasma erosion resistance, adhesion and wear resistance of the coating, thereby effectively reducing dust generation caused by coating peeling and extending the service life of the component. The main advantages of this new technology include: Enhanced plasma corrosion resistance: The combination of high-density surface modification layer and strong surface coating provides excellent plasma corrosion resistance, ensuring continuous and stable performance of components in harsh semiconductor process environments. Reduced particle contamination: By reducing coating peeling and substrate degradation, this new technology significantly reduces the generation of dust particles, thereby improving product quality and yield in the semiconductor manufacturing process. Material diversity and flexibility: This new technology can use a variety of substrate materials and a variety of deposition technologies, providing customized options for specific application requirements and process conditions. Improved mechanical properties: The multi-layer structure provides high hardness, high density and wear resistance, which together promote the durability and reliability of the components inside the cavity. Simplified manufacturing process: The use of advanced deposition technology and ion bombardment for surface modification simplifies the production of high-purity corrosion-resistant components, overcoming the limitations of traditional sintered ceramic and metal-based components. In summary, this new product provides an innovative solution to the challenges faced by semiconductor process equipment. By combining a tough substrate with professionally designed surface coatings and surface modification layers, this new product achieves enhanced durability, reduced contamination and improved overall performance to meet the growing needs of advanced semiconductor manufacturing technologies. In order to make the above features and advantages of the new model more obvious and easy to understand, the following is a detailed description of the preferred embodiment with the attached drawings.

請參照圖1,圖1所繪示為本新型之抗電漿侵蝕元件結構的其中一實施例。此抗電漿侵蝕侵蝕元件結構100(以下或稱元件結構100)旨在通過減輕電漿引起的侵蝕影響來增強腔體內部元件的耐用性及性能。抗電漿侵蝕侵蝕元件結構100包括一多層結構,其包括一基材110、一塗層120設置於該基材之一上表面、及一表面改質層130設置於該塗層上,綜合性地提供了卓越的抗電漿性能,減少了顆粒污染並延長了半導體製程腔體的使用壽命。 在抗電漿侵蝕元件結構100的基礎層為基材110,該基材110作為主要的結構支撐。基材110是選自一系列具有良好的機械強度、熱穩定性、及與半導體製程條件的相容性的材料。基材110材料的選擇標準包括:有效的熱傳導以散熱、在操作壓力下保持結構完整性的機械強度、阻止反應性電漿條件下降解的化學抗性,以及與後續塗層沉積方法的相容性以確保塗層120的有效沉積。適用的材料包括不鏽鋼合金如SUS304和SUS316,這些材料因其優異的抗腐蝕性和機械性能而受到青睞。此外,各種鋁合金,包括5000系列(含鎂合金)、6000系列(含鎂矽合金)、及7000系列(含鋅合金),因其強度、輕量化特性及熱傳導性而被選用。 基材110也可由陶瓷材料所構成,陶瓷材料例如為氧化鋁、氮化鋁、二氧化矽、碳化矽、氮化矽、二氧化鋯、及矽等材料。這些陶瓷材料因其高硬度、熱穩定性及優異的化學抗性,能夠耐受半導體製程中反應性電漿環境,此外高分子材料例如緩氧樹脂、聚乙烯等,亦可應用於其他特殊領域。 沉積於基材110上表面的塗層120在增強元件結構100的抗電漿磨損和腐蝕性方面起著關鍵作用。此塗層120顯著提高了元件結構100的硬度、耐磨性及抗腐蝕性,從而成為對抗電漿侵蝕的屏障。塗層120由選自金屬氧化物、氟化物及氮化物等材料所組成的群組,包括但不限於二氧化鈦、氧化鋁、氧化釔、氧化鉺、氧化釓、釔鋁石榴石、釔鋁單氧化物及鉺鋁石榴石。 塗層120通過沉積技術沉積在基材110的其中一表面上,所述沉積技術包括大氣等離子噴塗、懸浮等離子噴塗、真空等離子噴塗、氣溶膠噴塗、物理氣相沉積、原子層沉積或電漿增強化學氣相沉積。這些沉積技術允許對塗層120的厚度進行精確控制,厚度範圍通常在0.1 µm至250 µm之間,硬度範圍為400 HV至1500 HV。塗層120的孔隙率維持在1%至10%之間,確保機械強度與最小氣體滲透性之間的平衡。塗層120的效果進一步受到各種沉積參數的影響,這些沉積參數根據每種沉積方法而定。舉例來說,若為電漿噴塗技術,這些沉積參數包括:電弧電流、旋轉速度、載氣流量、預熱溫度及真空壓力。或者,若使用氣溶膠沉積技術,這些沉積參數包括:粉末粒徑、載氣流量、沉積壓力、噴塗溫度及噴嘴與基材110的距離。又或者,若使用物理氣相沉積技術,這些沉積參數包括:腔體溫度、蒸鍍速率、離子束功率和電壓、載氣流量及製程壓力。 表面改質層130位於了塗層120的上方,專門設計用來進一步增強抗電漿侵蝕性,通過增加表面密度及提高附著力來改善性能。該表面改質層130是通過離子轟擊進行緻密化處理而形成,顯著提升了塗層的性能。在離子轟擊過程中,是將塗層120暴露於由惰性氣體如氬氣、氪氣、氙氣或氡氣生成的離子流中。在其中一實施例中,這些離子在電流(100至3000 mA)、電壓(100至1500 V)、操作壓力(1.0E-1至1.0E-6 Torr)及氣體流量(5至500 Sccm)的控制條件下進行加速。 通過此離子轟擊過程,塗層120上方一部分的孔隙率降低至少50%以上,從而形成具有增強抗電漿侵蝕性、改良附著力及優異耐磨性的表面改質層130。經緻密化處理的表面改質層130的硬度範圍為500 HV至1500 HV,孔隙率低於1%,有效地減少了電漿滲透及後續材料劣化的途徑。表面改質層130與原始塗層120的厚度比例如是位於1%:99%~50%:50%這個範圍。 塗層120與表面改質層130之間的界面鍵結改進是維持多層組件完整性的關鍵,由於表面改質層130係藉由離子轟擊塗層120而產生,因此本身就具有很好的附著力,可有效降低塗層之剝離現象,減少微塵發生之機率。 接著,請參照圖2與圖3A至圖3C,圖2所繪示為本新型之抗電漿侵蝕元件結構的製造過程之其中一實施例,圖3A至圖3C所繪示為對應到圖2部分步驟的示意圖。首先,請參照步驟S110與圖3A,根據半導體製程環境的具體需求選擇基材110的材料。在其中一實施例中,基材110經過表面處理,包括清洗、去油脂及表面粗化,確保之後進行塗層120的沉積時有較佳的附著效果。 接著,請參照步驟S120與圖3B,在基材110選擇完成並清洗後,通過選擇的沉積方法(如APS、SPS、VPS、ADM、PVD、ALD或PECVD)於基材110之一上表面進行塗層120的沉積。沉積過程中的參數經過仔細控制,以達到指定範圍內的均勻塗層厚度,並賦予所需的硬度及孔隙率特性。在其中一實施例中,會進行步驟S130固化或受控冷卻,塗層120沉積後,可能需要進行固化或受控冷卻,以穩定塗層120。 隨後,請參照步驟S140與圖3C,在基材110準備完成後,通過離子轟擊塗層120以形成表面改質層130。將已塗覆塗層120的基材110置於配備惰性氣體源的離子轟擊腔體內。在電流、電壓、氣體流量及壓力的受控條件下,進行離子轟擊,以使塗層120形成一更緻密之表面改質層130,增強抗電漿侵蝕性。過程參數進行最佳化,確保塗層120表面有效緻密化而不損害其完整性。 在離子轟擊完成後,執性步驟S150,進行後處理步驟,包括熱處理以釋放應力並進一步增強塗層120與表面改質層130特性。隨後,執性步驟S160,對元件結構100進行嚴格的檢測,以確認塗層的均勻性、密度、硬度及附著力。檢測技術立足包括顯微鏡檢查、硬度測試及附著力測試。在其中一實施例中,如步驟S170所示,還可進行拋光或加工等修整步驟,以達到所需的尺寸及表面平滑度,確保元件結構100在半導體製程設備中的安裝。 本新型的元件結構100可實施於多種不同的應用。例如,一種實施例使用SUS304不鏽鋼作為基材110的材質,並通過大氣等離子噴塗形成150 µm厚度且材質為氧化鋁的塗層120。該塗有塗層120的基材110隨後經過500 mA、800 V的氬氣離子轟擊,進一步降低塗層表面之孔隙率。 在另一實施例中,基材110是由碳化矽這種陶瓷材質所製成,並通過懸浮等離子噴塗將70 wt%的氧化鋁(Al₂O₃)與30 wt%的二氧化鈦(TiO₂)的混合材質沉積成塗層120,厚度為200 µm。表面改質層130則通過1000 mA及1200 V的氙氣離子轟擊形成,使表面孔隙率降低。在又一實施例中,使用鋁合金作為基材110的材質,並通過物理氣相沉積沉積釔鋁石榴石以形成塗層120。在其中實施例中,也可以通過原子層沉積在以矽作為材質的基材110上沉積多種材料的塗層120。 上述這些實施例展示了不同的基材110材料、塗層組合及沉積技術如何結合,以滿足多樣的半導體製程需求。沉積方法的變化——如使用大氣等離子噴塗進行厚塗層、氣溶膠噴塗進行薄且緻密的塗層、物理氣相沉積進行薄且高硬度的塗層,或使用原子層沉積/電漿增強化學氣相沉積進行均勻的薄膜沉積——使得根據具體應用需求進行最佳化成為可能。 本新型的抗電漿侵蝕元件結構100相較於傳統腔體內部元件具有顯著優勢。首先,多層結構能有效抵禦電漿引起的侵蝕,從而保持結構完整性並減少頻繁更換元件的需求。此耐用性得益於高密度的表面改質層130,該表面改質層130在嚴苛的電漿環境下提供了卓越的保護。此外,塗層120與表面改質層130之間強勁的附著力能有效降低塗層顆粒的脫落,從而減少半導體製程環境中的顆粒污染。 抗電漿侵蝕元件結構100適用於廣泛的半導體製程設備,例如:電漿蝕刻腔體、化學氣相沉積(CVD)和物理氣相沉積(PVD)腔體、電漿增強光刻系統及離子植入設備中,亦即元件暴露於高能離子束及反應性電漿的環境中皆能受益於本新型所提供的增強侵蝕抵抗性及減少顆粒生成的特性。 雖然本新型已以較佳實施例揭露如上,然其並非用以限定本新型,任何所屬技術領域中具有通常知識者,在不脫離本新型之精神和範圍內,當可作些許之更動與潤飾,因此本新型之保護範圍當視後附之申請專利範圍所界定者為準。 Please refer to FIG. 1, which shows one embodiment of the novel plasma erosion resistant component structure. The plasma erosion resistant component structure 100 (hereinafter referred to as the component structure 100) is intended to enhance the durability and performance of components inside the chamber by reducing the erosion effect caused by plasma. The plasma erosion resistant component structure 100 includes a multi-layer structure, which includes a substrate 110, a coating 120 disposed on one upper surface of the substrate, and a surface modification layer 130 disposed on the coating, which comprehensively provides excellent plasma resistant performance, reduces particle contamination and prolongs the service life of the semiconductor process chamber. The base layer of the plasma erosion resistant device structure 100 is a substrate 110, which serves as the main structural support. The substrate 110 is selected from a series of materials with good mechanical strength, thermal stability, and compatibility with semiconductor process conditions. The selection criteria of the substrate 110 material include: effective thermal conductivity to dissipate heat, mechanical strength to maintain structural integrity under operating pressure, chemical resistance to prevent degradation under reactive plasma conditions, and compatibility with subsequent coating deposition methods to ensure effective deposition of the coating 120. Applicable materials include stainless steel alloys such as SUS304 and SUS316, which are favored for their excellent corrosion resistance and mechanical properties. In addition, various aluminum alloys, including 5000 series (containing magnesium alloys), 6000 series (containing magnesium-silicon alloys), and 7000 series (containing zinc alloys), are selected for their strength, lightweight properties, and thermal conductivity. The substrate 110 may also be made of ceramic materials, such as aluminum oxide, aluminum nitride, silicon dioxide, silicon carbide, silicon nitride, zirconium dioxide, and silicon. These ceramic materials can withstand the reactive plasma environment in the semiconductor process due to their high hardness, thermal stability, and excellent chemical resistance. In addition, polymer materials such as slow-oxidizing resins and polyethylene can also be used in other special fields. The coating 120 deposited on the upper surface of the substrate 110 plays a key role in enhancing the plasma wear and corrosion resistance of the device structure 100. This coating 120 significantly improves the hardness, wear resistance and corrosion resistance of the device structure 100, thereby becoming a barrier against plasma corrosion. The coating 120 is selected from a group consisting of materials such as metal oxides, fluorides and nitrides, including but not limited to titanium dioxide, aluminum oxide, yttrium oxide, geron oxide, gadolinium oxide, yttrium aluminum garnet, yttrium aluminum oxide and geron aluminum garnet. The coating 120 is deposited on one of the surfaces of the substrate 110 by a deposition technique, including atmospheric plasma spraying, suspension plasma spraying, vacuum plasma spraying, aerosol spraying, physical vapor deposition, atomic layer deposition, or plasma enhanced chemical vapor deposition. These deposition techniques allow the thickness of the coating 120 to be precisely controlled, typically ranging from 0.1 µm to 250 µm, and a hardness ranging from 400 HV to 1500 HV. The porosity of the coating 120 is maintained between 1% and 10%, ensuring a balance between mechanical strength and minimal gas permeability. The effect of the coating 120 is further affected by various deposition parameters, which are specific to each deposition method. For example, in the case of plasma spraying, these deposition parameters include: arc current, rotation speed, carrier gas flow rate, preheating temperature and vacuum pressure. Alternatively, in the case of aerosol deposition, these deposition parameters include: powder particle size, carrier gas flow rate, deposition pressure, spray temperature and distance between the nozzle and the substrate 110. Alternatively, in the case of physical vapor deposition, these deposition parameters include: chamber temperature, evaporation rate, ion beam power and voltage, carrier gas flow rate and process pressure. The surface modification layer 130 is located above the coating 120 and is specifically designed to further enhance the resistance to plasma erosion and improve performance by increasing surface density and improving adhesion. The surface modification layer 130 is formed by densification through ion bombardment, which significantly improves the performance of the coating. During the ion bombardment process, the coating 120 is exposed to an ion stream generated by an inert gas such as argon, krypton, xenon or radon. In one embodiment, these ions are accelerated under controlled conditions of current (100 to 3000 mA), voltage (100 to 1500 V), operating pressure (1.0E-1 to 1.0E-6 Torr) and gas flow rate (5 to 500 Sccm). Through this ion bombardment process, the porosity of a portion of the coating 120 is reduced by at least 50%, thereby forming a surface modification layer 130 with enhanced plasma corrosion resistance, improved adhesion and excellent wear resistance. The hardness of the densified surface modification layer 130 ranges from 500 HV to 1500 HV, and the porosity is less than 1%, which effectively reduces the path of plasma penetration and subsequent material degradation. The thickness ratio of the surface modification layer 130 to the original coating layer 120 is, for example, in the range of 1%:99% to 50%:50%. The improvement of the interface bonding between the coating layer 120 and the surface modification layer 130 is the key to maintaining the integrity of the multi-layer component. Since the surface modification layer 130 is generated by ion bombardment of the coating layer 120, it has good adhesion, which can effectively reduce the peeling phenomenon of the coating layer and reduce the probability of dust generation. Next, please refer to FIG. 2 and FIG. 3A to FIG. 3C. FIG. 2 shows one embodiment of the manufacturing process of the novel plasma erosion resistant component structure, and FIG. 3A to FIG. 3C show schematic diagrams corresponding to some steps of FIG. 2. First, please refer to step S110 and FIG. 3A to select the material of the substrate 110 according to the specific requirements of the semiconductor process environment. In one embodiment, the substrate 110 is surface treated, including cleaning, degreasing and surface roughening, to ensure better adhesion when the coating 120 is deposited later. Next, please refer to step S120 and FIG. 3B. After the substrate 110 is selected and cleaned, the coating 120 is deposited on one of the upper surfaces of the substrate 110 by a selected deposition method (such as APS, SPS, VPS, ADM, PVD, ALD or PECVD). The parameters in the deposition process are carefully controlled to achieve a uniform coating thickness within a specified range and to impart the desired hardness and porosity characteristics. In one embodiment, step S130 curing or controlled cooling is performed. After the coating 120 is deposited, curing or controlled cooling may be required to stabilize the coating 120. Subsequently, please refer to step S140 and FIG. 3C. After the substrate 110 is prepared, the coating 120 is bombarded by ions to form a surface modification layer 130. The substrate 110 coated with the coating 120 is placed in an ion bombardment chamber equipped with an inert gas source. Under controlled conditions of current, voltage, gas flow rate and pressure, ion bombardment is performed to form a more dense surface modification layer 130 on the coating 120 to enhance the resistance to plasma erosion. The process parameters are optimized to ensure that the surface of the coating 120 is effectively densified without damaging its integrity. After the ion bombardment is completed, a post-processing step is performed in step S150, including heat treatment to release stress and further enhance the properties of the coating 120 and the surface modification layer 130. Subsequently, a strict inspection of the component structure 100 is performed in step S160 to confirm the uniformity, density, hardness and adhesion of the coating. The inspection technology is based on microscopic inspection, hardness testing and adhesion testing. In one embodiment, as shown in step S170, finishing steps such as polishing or processing can also be performed to achieve the required size and surface smoothness to ensure the installation of the component structure 100 in the semiconductor process equipment. The new component structure 100 can be implemented in a variety of different applications. For example, one embodiment uses SUS304 stainless steel as the material of the substrate 110, and forms a coating 120 with a thickness of 150 µm and made of aluminum oxide by atmospheric plasma spraying. The substrate 110 coated with the coating 120 is then bombarded with argon ions at 500 mA and 800 V to further reduce the porosity of the coating surface. In another embodiment, the substrate 110 is made of a ceramic material such as silicon carbide, and a mixed material of 70 wt% aluminum oxide (Al₂O₃) and 30 wt% titanium dioxide (TiO₂) is deposited by suspended plasma spraying to form a coating 120 with a thickness of 200 µm. The surface modification layer 130 is formed by bombardment of xenon gas at 1000 mA and 1200 V to reduce the surface porosity. In another embodiment, an aluminum alloy is used as the material of the substrate 110, and yttrium aluminum garnet is deposited by physical vapor deposition to form the coating 120. In one embodiment, a coating 120 of multiple materials can also be deposited on a substrate 110 made of silicon by atomic layer deposition. The above embodiments show how different substrate 110 materials, coating combinations, and deposition techniques can be combined to meet a variety of semiconductor process requirements. Variations in deposition methods—such as using atmospheric plasma spraying for thick coatings, aerosol spraying for thin and dense coatings, physical vapor deposition for thin and high-hardness coatings, or using atomic layer deposition/plasma enhanced chemical vapor deposition for uniform thin film deposition—make it possible to optimize according to specific application requirements. The novel plasma erosion resistant component structure 100 has significant advantages over conventional chamber internal components. First, the multi-layer structure can effectively resist the erosion caused by plasma, thereby maintaining the structural integrity and reducing the need for frequent component replacement. This durability is due to the high-density surface modification layer 130, which provides excellent protection in harsh plasma environments. In addition, the strong adhesion between the coating 120 and the surface modification layer 130 can effectively reduce the shedding of coating particles, thereby reducing particle contamination in the semiconductor process environment. The plasma erosion resistant device structure 100 is applicable to a wide range of semiconductor process equipment, such as plasma etching chambers, chemical vapor deposition (CVD) and physical vapor deposition (PVD) chambers, plasma enhanced lithography systems, and ion implantation equipment. That is, devices exposed to high-energy ion beams and reactive plasma environments can benefit from the enhanced erosion resistance and reduced particle generation characteristics provided by the present invention. Although the present invention has been disclosed as above with the preferred embodiment, it is not intended to limit the present invention. Anyone with common knowledge in the relevant technical field can make some changes and modifications without departing from the spirit and scope of the present invention. Therefore, the protection scope of the present invention shall be subject to the scope defined in the attached patent application.

100:抗電漿侵蝕元件結構(元件結構) 110:基材 120:塗層 130:表面改質層 S110~S170:流程圖步驟100: Anti-plasma corrosion device structure (device structure) 110: Substrate 120: Coating 130: Surface modification layer S110~S170: Flow chart steps

圖1所繪示為本新型之抗電漿侵蝕元件結構的其中一實施例。 圖2所繪示為本新型之抗電漿侵蝕元件結構的製造過程之其中一實施例。 圖3A至圖3C所繪示為對應到圖2部分步驟的示意圖。 FIG. 1 shows one embodiment of the plasma erosion resistant component structure of the present invention. FIG. 2 shows one embodiment of the manufacturing process of the plasma erosion resistant component structure of the present invention. FIG. 3A to FIG. 3C show schematic diagrams corresponding to some steps of FIG. 2.

100:抗電漿侵蝕元件結構(元件結構) 100: Anti-plasma corrosion component structure (component structure)

110:基材 110: Base material

120:塗層 120: coating

130:表面改質層 130: Surface modification layer

Claims (7)

一種抗電漿侵蝕元件結構,包括: 一基材; 一塗層,設置於於所述基材之一表面;及 一表面改質層,設置於所述塗層上,該表面改質層之孔隙率小於該塗層之孔隙率,從而增強該元件抗電漿侵蝕性能。 A plasma erosion resistant component structure includes: a substrate; a coating disposed on a surface of the substrate; and a surface modification layer disposed on the coating, wherein the porosity of the surface modification layer is less than the porosity of the coating, thereby enhancing the plasma erosion resistance of the component. 如請求項1所述之抗電漿侵蝕元件結構,其中所述塗層經由以下至少一種沉積方法沉積:大氣等離子噴塗、懸浮等離子噴塗、真空等離子噴塗、氣溶膠噴塗、物理氣相沉積、原子層沉積、或電漿增強化學氣相沉積。The plasma erosion resistant component structure as described in claim 1, wherein the coating is deposited by at least one of the following deposition methods: atmospheric plasma spraying, suspension plasma spraying, vacuum plasma spraying, aerosol spraying, physical vapor deposition, atomic layer deposition, or plasma enhanced chemical vapor deposition. 如請求項1所述之抗電漿侵蝕元件結構,其中該基材的材質為金屬、高分子或陶瓷材料。The plasma erosion resistant component structure as described in claim 1, wherein the material of the substrate is metal, polymer or ceramic material. 如請求項1所述之抗電漿侵蝕元件結構,其中該表面改質層係藉由離子轟擊該塗層之上表面,以u降低其孔隙率而形成。A plasma erosion resistant component structure as described in claim 1, wherein the surface modification layer is formed by ion bombardment on the upper surface of the coating layer to reduce its porosity. 如請求項2所述之抗電漿侵蝕元件結構,其中該表面改質層的孔隙率較該塗層之孔隙率降低至少50%。A plasma erosion resistant component structure as described in claim 2, wherein the porosity of the surface modification layer is reduced by at least 50% compared to the porosity of the coating layer. 如請求項2所述之抗電漿侵蝕元件結構,其中所述表面改質層與所述塗層的厚度比介於以下範圍: 1:1~1:99。 The plasma erosion resistant component structure as described in claim 2, wherein the thickness ratio of the surface modification layer to the coating layer is in the following range: 1:1~1:99. 如請求項4所述之抗電漿侵蝕元件結構,其中所述表面改質層在所述離子轟擊中,係使用選自氬氣、氪氣、氙氣或氡氣的至少一種惰性氣體。The plasma erosion resistant device structure as described in claim 4, wherein the surface modification layer uses at least one inert gas selected from argon, krypton, xenon or radon during the ion bombardment.
TW113212130U 2024-11-07 2024-11-07 Plasma erosion resistant device structure TWM667354U (en)

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