KR19980015364A - Field effect transistor and manufacturing method thereof - Google Patents
Field effect transistor and manufacturing method thereof Download PDFInfo
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- KR19980015364A KR19980015364A KR1019960034661A KR19960034661A KR19980015364A KR 19980015364 A KR19980015364 A KR 19980015364A KR 1019960034661 A KR1019960034661 A KR 1019960034661A KR 19960034661 A KR19960034661 A KR 19960034661A KR 19980015364 A KR19980015364 A KR 19980015364A
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- 238000004519 manufacturing process Methods 0.000 title abstract description 7
- 238000002353 field-effect transistor method Methods 0.000 title 1
- 239000010408 film Substances 0.000 claims abstract description 123
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 52
- 229910052814 silicon oxide Inorganic materials 0.000 claims abstract description 50
- 239000010409 thin film Substances 0.000 claims abstract description 37
- 229910021420 polycrystalline silicon Inorganic materials 0.000 claims abstract description 27
- 238000000034 method Methods 0.000 claims abstract description 26
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims abstract description 17
- 229910052710 silicon Inorganic materials 0.000 claims abstract description 17
- 239000010703 silicon Substances 0.000 claims abstract description 17
- 230000015572 biosynthetic process Effects 0.000 claims abstract description 6
- 230000001066 destructive effect Effects 0.000 claims abstract description 3
- 238000005229 chemical vapour deposition Methods 0.000 claims description 22
- 229910052751 metal Inorganic materials 0.000 claims description 16
- 239000002184 metal Substances 0.000 claims description 16
- 229910052581 Si3N4 Inorganic materials 0.000 claims description 15
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 claims description 15
- 239000000758 substrate Substances 0.000 claims description 13
- 238000001020 plasma etching Methods 0.000 claims description 12
- 229920002120 photoresistant polymer Polymers 0.000 claims description 11
- 229910052785 arsenic Inorganic materials 0.000 claims description 9
- 238000004518 low pressure chemical vapour deposition Methods 0.000 claims description 9
- 229910052698 phosphorus Inorganic materials 0.000 claims description 8
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 7
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 claims description 7
- 238000009792 diffusion process Methods 0.000 claims description 7
- 230000003647 oxidation Effects 0.000 claims description 7
- 238000007254 oxidation reaction Methods 0.000 claims description 7
- 239000011574 phosphorus Substances 0.000 claims description 7
- 238000005530 etching Methods 0.000 claims description 5
- 238000005498 polishing Methods 0.000 claims description 5
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 claims description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 4
- 238000002955 isolation Methods 0.000 claims description 4
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 3
- 238000000151 deposition Methods 0.000 claims description 3
- 230000001590 oxidative effect Effects 0.000 claims description 3
- 239000004065 semiconductor Substances 0.000 claims description 3
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 2
- 230000008021 deposition Effects 0.000 claims description 2
- 238000005240 physical vapour deposition Methods 0.000 claims description 2
- 238000001039 wet etching Methods 0.000 claims description 2
- 150000002500 ions Chemical class 0.000 claims 2
- 239000000126 substance Substances 0.000 claims 2
- 238000002488 metal-organic chemical vapour deposition Methods 0.000 claims 1
- 230000005669 field effect Effects 0.000 abstract description 15
- 230000005621 ferroelectricity Effects 0.000 abstract description 5
- 239000012535 impurity Substances 0.000 abstract description 5
- 238000010438 heat treatment Methods 0.000 abstract description 4
- 238000006243 chemical reaction Methods 0.000 abstract description 3
- 239000000463 material Substances 0.000 abstract description 3
- 230000004888 barrier function Effects 0.000 abstract 1
- 238000010586 diagram Methods 0.000 description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 239000003990 capacitor Substances 0.000 description 2
- 230000006870 function Effects 0.000 description 2
- 229910044991 metal oxide Inorganic materials 0.000 description 2
- 150000004706 metal oxides Chemical class 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 230000010287 polarization Effects 0.000 description 2
- 230000002269 spontaneous effect Effects 0.000 description 2
- 230000003068 static effect Effects 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
- 230000003213 activating effect Effects 0.000 description 1
- 229910021417 amorphous silicon Inorganic materials 0.000 description 1
- 230000005685 electric field effect Effects 0.000 description 1
- 238000005468 ion implantation Methods 0.000 description 1
- 238000005121 nitriding Methods 0.000 description 1
- 229920005591 polysilicon Polymers 0.000 description 1
- 229910021332 silicide Inorganic materials 0.000 description 1
- FVBUAEGBCNSCDD-UHFFFAOYSA-N silicide(4-) Chemical compound [Si-4] FVBUAEGBCNSCDD-UHFFFAOYSA-N 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- OFIYHXOOOISSDN-UHFFFAOYSA-N tellanylidenegallium Chemical compound [Te]=[Ga] OFIYHXOOOISSDN-UHFFFAOYSA-N 0.000 description 1
- 238000007740 vapor deposition Methods 0.000 description 1
Classifications
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- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10D—INORGANIC ELECTRIC SEMICONDUCTOR DEVICES
- H10D30/00—Field-effect transistors [FET]
- H10D30/01—Manufacture or treatment
- H10D30/021—Manufacture or treatment of FETs having insulated gates [IGFET]
- H10D30/0415—Manufacture or treatment of FETs having insulated gates [IGFET] of FETs having ferroelectric gate insulators
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table or AIIIBV compounds with or without impurities, e.g. doping materials
- H01L21/28—Manufacture of electrodes on semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/268
- H01L21/283—Deposition of conductive or insulating materials for electrodes conducting electric current
- H01L21/285—Deposition of conductive or insulating materials for electrodes conducting electric current from a gas or vapour, e.g. condensation
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table or AIIIBV compounds with or without impurities, e.g. doping materials
- H01L21/30—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26
- H01L21/302—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26 to change their surface-physical characteristics or shape, e.g. etching, polishing, cutting
- H01L21/304—Mechanical treatment, e.g. grinding, polishing, cutting
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table or AIIIBV compounds with or without impurities, e.g. doping materials
- H01L21/30—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26
- H01L21/302—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26 to change their surface-physical characteristics or shape, e.g. etching, polishing, cutting
- H01L21/306—Chemical or electrical treatment, e.g. electrolytic etching
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- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10B—ELECTRONIC MEMORY DEVICES
- H10B12/00—Dynamic random access memory [DRAM] devices
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- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10D—INORGANIC ELECTRIC SEMICONDUCTOR DEVICES
- H10D30/00—Field-effect transistors [FET]
- H10D30/60—Insulated-gate field-effect transistors [IGFET]
- H10D30/701—IGFETs having ferroelectric gate insulators, e.g. ferroelectric FETs
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Abstract
본 발명은 커패시터가 없는 기억 소자(capacitorless memory device), 특히 강유전 박막을 게이트 유전막으로 채택한 비파괴성 판독기(non-destructive read-out)형 전계효과 트랜지스터의 구조 및 그 제조방법을 제공하는 것으로서, 종래의 트랜지스터의 소오스/드레인의 형성을 위하여 불순물의 활성화를 하는데 있어서, 현재 사용되고 있는 공정에서는 고온의 열처리가 필요하기 때문에 고온에서 강유전성을 잃어버리는 강유전 박막을 게이트 막으로 채택하기가 불가능하고 지금까지 이용되어온 산화물들을 게이트 유전막으로 이용하면 규소 계면에 자연 산화물이 형성됨으로 강유전성을 얻기가 어렵기 때문에, 다결정규소 소오스/드레인이 먼저 형성되고 게이트 전극이 금속계로 형성되며, 게이트 유전막이 비산화물 강유전 박막으로 대치되면 게이트 유전막과 다결정규소 소오스/드레인은 규소산화막에 의해 차폐되어 두 재료 사이에 가능한 반응이나 전류 누설을 억제함으로써 트랜지스터의 전계 효과를 증가시킨다.Disclosed is a structure of a non-destructive read-out type field effect transistor employing a capacitorless memory device, particularly a ferroelectric thin film as a gate dielectric film, and a method of manufacturing the same. In order to activate the impurities for the formation of the source / drain of the transistor, a ferroelectric thin film which loses its ferroelectricity at high temperature can not be adopted as a gate film because a heat treatment at a high temperature is required in a process currently used, It is difficult to obtain ferroelectricity because natural oxide is formed on the silicon interface. Therefore, when the gate dielectric film is replaced with a non-oxide ferroelectric thin film, polycrystalline silicon source / drain is formed first, It's a dielectric barrier. Regular small source / drain increases the field-effect transistor by suppressing the reaction and current leakage possible between the two materials is shielded by the silicon oxide film.
Description
제1도는 종래의 강유전체 메모리 소자의 등가회로도.FIG. 1 is an equivalent circuit diagram of a conventional ferroelectric memory device. FIG.
제2도는 본 발명에 의한 강유전 트랜지스터의 설계도.FIG. 2 is a schematic diagram of a ferroelectric transistor according to the present invention. FIG.
제3도는 본 발명에 따른 강유전체 트랜지스터의 단면도.3 is a cross-sectional view of a ferroelectric transistor according to the present invention;
제4도의 (a) 내지 (k)는 본 발명의 강유전체 트랜지스터의 제조 단면도.4 (a) to 4 (k) are cross-sectional views of a ferroelectric transistor according to the present invention.
*도면의 주요 부분에 대한 부호의 설명*Description of the Related Art [0002]
1 : 규소기판(Silicon substrate)2 : 활성영역(active region)1: Silicon substrate 2: active region
3: 격리영역(isolation region)3: isolation region
3a,3b,3c,3d,5a,5b,5c,5d,5e,5f,9,9a,11,11a,11b,11c,14a,14b,16a,16b,16c : 규소 산화막(silicon oxide)4 : 다결정규소막A silicon oxide 4: a silicon oxide film 4: a silicon oxide film 4: a silicon oxide film 4: a silicon oxide film 4: a silicon oxide film 4: a silicon oxide film 5: Polycrystalline silicon film
4a,4b : 다결정규소(또는 폴리사이드) 소오스/드레인4a and 4b: polycrystalline silicon (or polycide) source / drain
6a,6b : 소오스/드레인 확산층(source/drain diffusion layer)6a and 6b: a source / drain diffusion layer,
7,15 : 게이트 유전막(dielectric film)7, 15: gate dielectric film
8 : 금속 게이트 전극(metal gate electrode)8: Metal gate electrode
10,10a,10b,10c : 규소질화막(silicon nitride)10, 10a, 10b, 10c: a silicon nitride film,
12a,12b : 감광막(photoresist)12a, 12b: photoresist
17a,17b : 금속전극(metal electrode)17a and 17b: a metal electrode,
본 발명은 트랜지스터 및 그 제조방법에 관한 것으로서, 특히 강유전체를 게이트 유전막으로 사용한 전계효과 트랜지스터 및 그 제조방법에 관한 것이다.The present invention relates to a transistor and a manufacturing method thereof, and more particularly, to a field effect transistor using a ferroelectric as a gate dielectric film and a method of manufacturing the same.
종래의 강유전 전계효과 트랜지스터는 제1도의 (a)에 나타낸 바와 같이, 강유전체 박막(ferroelectric thin film)을 게이트 박막으로 사용하여 이 강유전체 박막의 자발 분극의 방향에 의하여 전계효과 트랜지스터의 소오스/드레인 간의 저항의 변화를 검출함으로써 메모리 소자에 응용하는 방법이 연구되었다.As shown in FIG. 1 (a), a conventional ferroelectric field effect transistor uses a ferroelectric thin film as a gate thin film, and the resistance between the source and the drain of the field effect transistor by the spontaneous polarization direction of the ferroelectric thin film A method of applying the method to a memory device has been studied.
또한 제1도의 (b)에 도시된 바와 같이, 다이나믹 램(dynamic random access memory, DRAM) 소자 구조에서 저장 용량기의 유전막을 강유전체로 함으로써 재충전 시간을 아주 길게 할 수 있다.Also, as shown in FIG. 1 (b), the dielectric film of the storage capacitor in the dynamic random access memory (DRAM) device structure can be made ferroelectric to make the recharging time very long.
상기에 따라 스태틱 램(static random access memory, SRAM)과 동일한 기능을 할 뿐만 아니라, 읽고 쓰기 횟수가 늘어나 기존의 전기적으로 삭제 가능한 피롬(electrically erasable programmable read only memory, EEPROM)보다 우수한 성능을 발휘할 수 있다.According to the above, the SRAM has the same function as the static random access memory (SRAM), and the erasable programmable read only memory (EEPROM) is superior in performance to the erasable programmable read only memory .
하지만 제1도 (a) 구조의 전계효과 트랜지스터의 소오스/드레인의 형성을 위하여 불순물의 활성화를 하는데 있어서, 현재 널리 사용되고 있는 공정에서는 고온(850℃ 이상)의 열처리가 필요하기 때문에 고온에서 강유전성을 잃어버리는 강유전 박막을 게이트 유전막으로 채택하기가 불가능하였다. 또한, 현재까지 강유전 박막으로 알려진 대부분은 BaTiO3와 PbTiO3,그리고 PZT와, KNbO3등의 페롭스카이트(perobskite)형의 산화물이다. 따라서 상기의 산화물들을 바로 게이트 유전막으로 이용하면 규소 계면에 자연산화물이 형성되므로 규소 위에서는 강유전성을 얻기가 매우 어렵다.However, in order to activate impurities for the formation of the source / drain of the field-effect transistor having the structure (a) in FIG. 1, since heat treatment at a high temperature (850 ° C. or more) is required in the currently widely used process, ferroelectricity is lost at high temperature It was impossible to adopt a ferroelectric thin film as a gate dielectric film. In addition, most of the ferroelectric thin films known to date are perovskite type oxides such as BaTiO 3 , PbTiO 3, PZT, and KNbO 3 . Therefore, when the oxides are directly used as a gate dielectric film, natural oxides are formed at the silicon interface, and it is very difficult to obtain ferroelectricity on silicon.
상기한 이유로 강유전 박막을 형성한 후 고온 공정이 필요하지 않는 트랜지스터 구조가 필수적이며, 비산화물계 강유전 박막이 필요하게 되었다.For the above reasons, a transistor structure which does not require a high-temperature process after forming a ferroelectric thin film is indispensable, and a non-oxide-based ferroelectric thin film is required.
또한 상기 비산화물계 강유전 박막은 현재 BaMgF4등이 개발되어 박막화와 성능 개선을 꾀하고 있다. 따라서 강유전 박막을 형성한 후, 고온 공정이 필요하지 않는 전계효과 트랜지스터 구조가 요구되고 있다.In addition, BaMgF 4 and the like have been developed in the nonoxide-based ferroelectric thin film to improve the thinning performance and the performance. Therefore, there is a demand for a field effect transistor structure in which a ferroelectric thin film is formed and then a high temperature process is not required.
본 발명은 상기한 점을 감안하여 발명된 것으로서, 커패시터가 없는 기억 소자(capacitorless memory deivce), 특히 강유전체의 박막을 게이트 유전막으로 채택한 비파괴성 판독형(non-destructive read-out) 전계효과 트랜지스터 및 그 제조방법을 제공하는데 그 목적이 있다.Disclosure of the Invention The present invention has been made in view of the above-mentioned problems, and it is an object of the present invention to provide a non-destructive read-out field effect transistor employing a capacitorless memory deivce, particularly a ferroelectric thin film as a gate dielectric film, And a manufacturing method thereof.
상기 목적을 달성하기 위하여 본 발명에 따른 전계효과 트랜지스터는 게이트 전극이 금속계로 형성되고, 또한 게이트 유전막이 비산화물계인 강유전체 박막으로 이루어지는 것을 특징으로 한다.In order to achieve the above object, a field-effect transistor according to the present invention is characterized in that a gate electrode is formed of a metal system and a gate dielectric film is a non-oxide-type ferroelectric thin film.
이하, 첨부된 도면을 참조하여 상세히 설명하면 다음과 같다.Hereinafter, the present invention will be described in detail with reference to the accompanying drawings.
제1도는 종래의 강유전체 메모리 소자의 등가회로도로서, 제1도의 (가)는 강유전체 박막을 게이트 유전막으로 사용하여 이 강유전체 박막의 자발분극의 방향에 의한 전계효과 트랜지스터 소오스/드레인 간의 저항의 변화를 검출함으로써 메모리 소자에 응용하는 방법이 연구되고 있다.FIG. 1 is an equivalent circuit diagram of a conventional ferroelectric memory device. In FIG. 1 (a), a ferroelectric thin film is used as a gate dielectric film to detect a change in resistance between a source and a drain of a field effect transistor due to the spontaneous polarization direction of the ferroelectric thin film A method for application to a memory device is being studied.
또한 제1도의 (b)는 다이나믹 램(dynamic random access memory, DRAM) 소자 구조에서 저장 용량기의 유전막을 강유전체로 함으로써 재충전 시간을 아주 길게 하여 스태틱 램(static random access memory, SRAM)과 동일한 기능을 할 뿐만 아니라, 읽고 쓰기 횟수가 늘어나 기존의 전기적으로 삭제 가능한 피롬(EEPROM) 보다 우수한 성능을 발휘할 수 있다. 하지만 상기 (a) 구조에서, 전계효과 트랜지스터의 소오스/드레인의 형성을 위하여 불순물의 활성화를 하는데 있어서 현재 널리 사용되고 있는 공정에서는 고온(850℃ 이상)의 열처리가 필요하기 때문에 고온에서 강유전성을 잃어버리는 강유전 박막을 게이트 유전막으로 채택하기가 불가능하였다. 또한, 현재까지 강유전 박막으로 알려진 대부분은 BaTiO3와, PbTiO3와, PZT와, KNbO3등의 페롭스카이트(perobskite)-형의 산화물이다.FIG. 1 (b) shows the same function as a static random access memory (SRAM) by making the recharge time very long by making the dielectric film of the storage capacitor a ferroelectric in a dynamic random access memory (DRAM) In addition to increasing the number of read and write, it can perform better than conventional electrically erasable programmable read only memory (EEPROM). However, in the above structure (a), since a heat treatment at a high temperature (850 DEG C or more) is required in a currently widely used process for activating impurities for forming a source / drain of a field effect transistor, a ferroelectric It was impossible to adopt a thin film as a gate dielectric film. In addition, most of the ferroelectric thin films known to date are perovskite-type oxides such as BaTiO 3 , PbTiO 3 , PZT, and KNbO 3 .
상기의 산화물들을 바로 게이트 유전막으로 이용하면 규소 계면에 자연산화물이 형성됨으로써 규소 위에서는 강유전성을 얻기가 매우 어렵다.If the oxides are directly used as a gate dielectric film, a native oxide is formed at the silicon interface, and it is very difficult to obtain ferroelectricity on silicon.
상기한 이유로 강유전 박막을 형성한 후 고온 공정이 필요하지 않는 트랜지스터 구조가 필수적이며, 비산화물계 강유전 박막이 필요하게 되었다.For the above reasons, a transistor structure which does not require a high-temperature process after forming a ferroelectric thin film is indispensable, and a non-oxide-based ferroelectric thin film is required.
상기에 따라 비산화물계 강유전 박막은 현재 BaMgF4등이 개발되어서 박막화와 성능 개선을 꾀하고 있다. 따라서 강유전 박막을 형성한 후 고온 공정이 필요하지 않는 전계효과 트랜지스터 구조가 요구되고 있다.As described above, BaMgF 4 and the like have been developed in non-oxide based ferroelectric thin films to improve thinning performance and performance. Therefore, there is a demand for a field effect transistor structure in which a ferroelectric thin film is formed and a high temperature process is not required.
제2도는 본 발명에 의한 강유전 트랜지스터의 설계도이다. 상기의 구조는, 다결정규소(또는 폴리사이드)(4a,4b)를 소오스/드레인으로 한 전계효과 트랜지스터의 설계도를 나타낸 것이다.FIG. 2 is a schematic diagram of a ferroelectric transistor according to the present invention. The above structure shows a design of a field effect transistor in which polycrystalline silicon (or polycide) 4a, 4b is used as a source / drain.
제3도는 본 발명에 따른 강유전체 트랜지스터의 단면도로서, 상기 제2도의 구조를 A-A´ 선을 따라 단면을 나타낸 것이다. 상기에 따라, 트랜지스터간의 격리는 홈-형의 규소산화막(3a,3b)에 의하여 이루어지고, 소오스/드레인 확산층(source/drain diffusion layer)(6a,6b)의 형성은 다결정규소(또는 폴리사이드)(4a,4b)에 함유된 인(P)과 비소(As) 불순물이 규소기판(1)으로 확산하면서 각각 n-와 n+확산층을 형성함으로써 이루어진다. 또한 게이트 유전막(7)은 강유전체로 이루어졌으며, 게이트 유전막(7)과 다결정규소(또는 폴리사이드) 소오스/드레인(4a,4b)은 규소산화막(5a,5b)에 의하여 차폐되어 두 재료 사이에 가능한 반응이나 전류누설을 억제한다.FIG. 3 is a cross-sectional view of a ferroelectric transistor according to the present invention, showing the structure of FIG. 2 along a line AA '. The source / drain diffusion layers 6a and 6b are formed by polycrystalline silicon (or polycide), and the source / drain diffusion layers 6a and 6b are formed by the silicon- (P) and arsenic (As) impurities contained in the silicon substrate (4a, 4b) diffuse into the silicon substrate (1) while forming n - and n + diffusion layers, respectively. The gate dielectric film 7 is made of a ferroelectric material and the gate dielectric film 7 and polycrystalline silicon (or polycide) source / drain regions 4a and 4b are shielded by the silicon oxide films 5a and 5b, And suppresses the reaction or current leakage.
또한, 상기 금속 게이트 전극(metal gate electrode)(8)은 금속 산화막 반도체(Metal-Oxide Semiconductor, MOS) 트랜지스터에서 일반적으로 많이 사용되는 다결정규소가 아니라 금속으로 이루어진다.In addition, the metal gate electrode 8 is not made of polycrystalline silicon, which is generally used in a metal-oxide semiconductor (MOS) transistor, but is made of metal.
다음의 제4a도에서 제4k도는 본 발명의 강유전체 트랜지스터의 제조 단면도이다. 상기의 공정순서를 보면 먼저, a는 규소기판(silicon substrate)(1)에 규소산화막(3a,3b)에 의하여 격리를 형성한 것을 나타낸 것이다. 상기의 구조를 보면, P-형 규소기판(1)에 열산화 또는 화학 기상 증착(chemical vapor deposition, CVD)에 의하여 규소산화막(3a,3b)을 형성한 뒤 활성 마스크(active mask)작업을 수행하여 격리영역(isolation region)(3)의 감광막을 제거한다. 상기 감광막(photoresist)의 제거 후 산화막(3a,3b)과 규소기판(1)을 반응성 이온 에칭(reactive ion etching, RIE)에 의하여 홈을 형성한 뒤 홈의 표면을 열산화하고 화학 기상 증착(CVD) 규소산화막에 의하여 홈을 채운 뒤 역-에치(etch-back)나 화학-기계적 연마(chemical-mechanical polishing, CMP)에 의하여 표면을 평탄하게 하면 상기 제4도의 a와 같은 구조가 형성된다.4a to 4k are cross-sectional views of the ferroelectric transistor of the present invention. In the above-mentioned process sequence, a shows that the silicon substrate 1 is formed by the silicon oxide films 3a and 3b. In the above structure, the silicon oxide films 3a and 3b are formed on the P-type silicon substrate 1 by thermal oxidation or chemical vapor deposition (CVD), and an active mask operation is performed Thereby removing the photosensitive film of the isolation region 3. After the removal of the photoresist, the oxide films 3a and 3b and the silicon substrate 1 are formed by reactive ion etching (RIE) to form a groove. Then, the surface of the groove is thermally oxidized, and chemical vapor deposition (CVD) ) Grooves are filled with a silicon oxide film and then the surface is planarized by etch-back or chemical-mechanical polishing (CMP) to form the structure shown in FIG. 4 (a).
상기 제4도의 b는 상기 a의 구조 위에 열산화막 또는 화학 기상 증착(CVD) 산화막(9)을 형성한 뒤 저압 화학 기상 증착(low pressure LPCVD)에 의하여 규소질화막(silicon nitride)(10)과 화학 기상 증착(CVD) 규소산화막(11)을 차례로 형성한 것을 나타낸 것이다. 상기 규소산화막(9)의 두께는 10∼30nm으로서, 열산화는 확산로(diffusion furnace)에서 850℃의 온도와 산소 분위기에서 15∼30분간 수행된다. 또한 상기 규소질화막(10)의 두께는 20∼50nm으로서, 저압 화학 기상 증착(LPCVD)로에서 825℃의 온도와 SiH4/NH3/H2분위기에서 질화가 수행된다.FIG. 4 (b) is a cross-sectional view of a silicon nitride film 10 formed by a low pressure LPCVD process after forming a thermal oxide film or a chemical vapor deposition (CVD) And a vapor deposition (CVD) silicon oxide film 11 are sequentially formed. The thickness of the silicon oxide film 9 is 10 to 30 nm, and thermal oxidation is performed in a diffusion furnace at a temperature of 850 DEG C and an oxygen atmosphere for 15 to 30 minutes. In addition, the thickness of the silicon nitride film 10 as a 20~50nm, the nitriding is carried out at a temperature of 825 ℃ in a low pressure chemical vapor deposition (LPCVD), and SiH 4 / NH 3 / H 2 atmosphere.
그리고 상기 규소산화막(11)의 두께는 200∼400nm로서, 화학 기상 증착(CVD)로에서 SiH4/O2분위기에서 산화가 수행된다.The thickness of the silicon oxide film 11 is 200 to 400 nm, and oxidation is performed in a SiH 4 / O 2 atmosphere by chemical vapor deposition (CVD).
제4도의 c는 소오스/드레인 마스크 작업을 수행하여 소오스/드레인 영역의 감광막을 제거한 것을 나타낸 것이다.FIG. 4C shows removal of the photoresist film of the source / drain region by performing a source / drain mask operation.
이에 따라 소오스/드레인 영역외에서는 감광막(12a,12b,12c)이 남게된다.Accordingly, the photoresist films 12a, 12b, and 12c remain outside the source / drain regions.
다음의 제4도 d는 반응성 이온 에칭(reactive ion etching, RIE)에 의하여 소오스/드레인 영역의 규소산화막(11)과, 규소질화막(10), 그리고 규소산화막(9)을 차례로 식각한 것을 나타낸 것이다.FIG. 4 (d) shows the silicon oxide film 11, the silicon nitride film 10, and the silicon oxide film 9 of the source / drain region are sequentially etched by reactive ion etching (RIE) .
상기의 공정에 의하여 소오스/드레인이 형성될 규소기판(1)이 노출된다.By the above process, the silicon substrate 1 on which the source / drain is to be formed is exposed.
제4도의 e는 상기의 감광막(12a,12b,12c)을 제거한 뒤 저압 화학기상 증착(LPCVD)에 의하여 다결정규소막(4)을 형성한 것을 나타낸 것인데, 다결정규소 대신에 비정질규소를 증착하여도 무방하다.4 shows that the polycrystalline silicon film 4 is formed by low pressure chemical vapor deposition (LPCVD) after removing the photoresist films 12a, 12b and 12c described above. Even if amorphous silicon is deposited instead of polycrystalline silicon It is acceptable.
그리고 상기 다결정규소막(4)의 두께가 상기 규소산화막(11a,11b,11c)의 높이보다 50∼100nm 정도 두껍게 한다.The thickness of the polycrystalline silicon film 4 is about 50 to 100 nm thicker than the silicon oxide films 11a, 11b, and 11c.
제4도의 f는 화학-기계적 연마(CMP)에 의하여 상기 다결정규소막(4)을 평탄케 하되, 상기의 규소산화막(11a,11b,11c)이 노출될 때까지 수행한다.In FIG. 4F, the polycrystalline silicon film 4 is flattened by chemical-mechanical polishing (CMP) until the silicon oxide films 11a, 11b and 11c are exposed.
상기 화학-기계적 연마(CMP)에는 KOH 용액과 실리카를 혼합한 슬러리(slurry)가 이용된다.For the chemical-mechanical polishing (CMP), a slurry obtained by mixing a KOH solution and silica is used.
상기의 과정에서 다결정규소막과 규소산화막의 연마비는 20 : 1 이상이므로 상기의 규소산화막(11a,11b,11c)은 거의 연마되지 않는다.In the above process, the silicon oxide films 11a, 11b, and 11c are hardly polished because the etching rate of the polycrystalline silicon film and the silicon oxide film is 20: 1 or more.
또한 다음 기술과 반대 형의 N-형 불순물인 인(P)과 비소(AS)를 이온주입하되 인의 도우즈는 5∼20 × 1012㎝-2이고, 에너지는 50∼80 KeV로 하고, 비소의 도오즈는 2∼6 × 1015㎝-2이고, 에너지는 50∼100 KeV로 한다.In addition, phosphorus (P) and arsenic (AS), which are the N-type impurities of the opposite type, are ion-implanted while the phosphorus dose is 5 to 20 × 10 12 cm -2 , the energy is 50 to 80 KeV, The ozone concentration is 2 to 6 × 10 15 cm -2 and the energy is 50 to 100 keV.
그런데 인과 비소의 이온-주입은 상기 제4도 e의 단계에서 수행하여도 무방하다.However, the ion-implantation of phosphorus and arsenic may be performed in the step of FIG.
상기한 단계 수행이후 다결정규소에 금속을 증착한 후 열처리함으로써 폴리사이드(polycide; 실리콘 집적회로의 게이트 전극에 사용하는 금속 규화물과 다결정 실리콘막으로 이루어지는 2층 구조물)를 형성할 수도 있다.After the above steps are performed, a polycide (a metal silicide used for the gate electrode of the silicon integrated circuit and a two-layer structure including the polysilicon film) may be formed by depositing a metal on the polycrystalline silicon and then performing heat treatment.
다음 제4도의 g는 소오스/드레인 영역에 형성된 다결정규소(4a,4b)를 열산화하여 30∼50nm의 규소산화막(14a,14b)을 형성한 것을 나타낸 것인데, 채널 영역은 규소질화막(10b)에 의하여 열산화되지 않는다.G in the following FIG. 4 shows that the silicon oxide films 14a and 14b of 30 to 50 nm are formed by thermally oxidizing the polycrystalline silicon 4a and 4b formed in the source / drain region. The channel region is formed in the silicon nitride film 10b It is not thermally oxidized.
상기의 열산화는 고온로에서 850℃이고, 산소 분위기에서 20∼60분간 수행된다.The above thermal oxidation is carried out at a high temperature of 850 DEG C for 20 to 60 minutes in an oxygen atmosphere.
상기의 과정에서 다결정규소(4a,4b)내에 포함된 인과 비소가 규소기판(1)내로 확산하여 소오스/드레인(6a,6b)을 형성한다.In the above process, phosphorus and arsenic contained in the polycrystalline silicon 4a and 4b diffuse into the silicon substrate 1 to form the source / drain 6a and 6b.
그리고 인은 비소보다 더 깊이 확산하여 n-층을 형성하고, 비소는 인보다 작게 확산하여 고농도의 n+층을 형성한다.And phosphorus diffuses deeper than arsenic to form n - layer, and arsenic diffuses less than phosphorus to form high concentration n + layer.
다음의 제4도의 h는 인산 용액을 이용하여 상기의 규소질화막(10a,10b,10c)을 제거한 뒤 불산 용액을 이용하여 상기의 규소산화막(9a)을 제거한 것을 나타낸 것이다.FIG. 4 (h) in the following figure shows removal of the above silicon nitride films 10a, 10b and 10c by using a phosphoric acid solution and removal of the silicon oxide films 9a by using a hydrofluoric acid solution.
이 과정에서 상기의 산화막(14a,14b)은 다소 식각되어 원래보다 얇아져 규소산화막(5a,5b)의 두께는 20∼40nm가 된다.In this process, the oxide films 14a and 14b are etched to be thinner than the original thickness, and the thicknesses of the silicon oxide films 5a and 5b become 20 to 40 nm.
상기의 규소산화막(5a,5b)은 강유전 박막이 다결정규소 소오스/드레인과 반응하는 것과 게이트/드레인 중첩 커패시턴스가 커지는 것을 방지하는 역할을 한다.The silicon oxide films 5a and 5b serve to prevent the ferroelectric thin film from reacting with the polycrystalline silicon source / drain and the gate / drain superposed capacitance from becoming large.
다음 제4도의 i는 게이트 절연막으로서 게이트 유전막(15)을 형성한 것을 나타낸 것이다.4 (i) in the following figure shows that the gate dielectric film 15 is formed as the gate insulating film.
상기의 게이트 유전막(15)으로서는 산화물계 강유전체와, 산화막과 강유전체 박막의 2층 구조, 또는 규소와 반응하여 산화물을 형성하지 않는 비산화물계 강유전 박막을 선택한다.As the gate dielectric film 15, a non-oxide-based ferroelectric thin film which does not form an oxide by reacting with an oxide-based ferroelectric, a two-layer structure of an oxide film and a ferroelectric thin film, or silicon is selected.
예를 들어 극초진공(ultra high vacuum, UHV) 화학 기상 증착(CVD)에 의하여 BaMgF4을 규소기판 위에 증착한다.For example, BaMgF 4 is deposited on a silicon substrate by ultra high vacuum (UHV) chemical vapor deposition (CVD).
다음의 제4도의 j는 게이트 유전막(7)과 게이트 전극(8)을 형성한 것을 나타낸 것이다.4 (j) shows that the gate dielectric film 7 and the gate electrode 8 are formed.
상기의 게이트 유전막(15) 위에 물리적 기상 증착법(physical vapor deposition)이나 유기금속 화학 기상 증착(metal organic CVD, MOCVD)에 의하여 금속(W, Al 혹은 Al/TiW, Cu/TiN 등의 다층 금속)을 500∼1000nm 증착한 뒤 게이트 마스크 작업을 수행하여 감광막을 게이트 영역에 남긴 뒤 반응성 이온 에치(RIE) 또는 습식 식각에 의하여 상기의 금속과 게이트 유전막(15)을 식각하여 게이트 유전막(7)과 게이트 전극(8)을 형성한다.A metal (W, Al or Al / TiW, a multilayer metal such as Cu / TiN) is deposited on the gate dielectric layer 15 by physical vapor deposition or metal organic chemical vapor deposition After the deposition of 500 to 1000 nm, a gate mask operation is performed to leave the photoresist film in the gate region. Then, the metal and the gate dielectric film 15 are etched by reactive ion etching (RIE) or wet etching to form the gate dielectric film 7 and the gate electrode (8).
그리고 콘택트의 형성과 금속 배선의 형성 등 일반적인 금속 산화막 반도체(MOS) 공정에 의하여 소오스 전극(16a)와 드레인 전극(16b)을 형성한 것을 나타낸 것이다.And the source electrode 16a and the drain electrode 16b are formed by a general metal oxide semiconductor (MOS) process such as formation of a contact and formation of a metal wiring.
상기와 같이 설명한 바에 따라 전계효과 트랜지스터 및 그 제조방법은, 다결정규소 소오스/드레인을 FET(field-effect transistor)에 적용하고 게이트 유전막과 다결정규소 소오스/드레안은 규소산화막(silicon oxide)에 의하여 차폐되어 두 재료 사이에 가능한 반응이나 전류누설을 억제함으로써 트랜지스터의 전계효과를 증가시킬 수 있는 제조방법을 실현할 수 있다.As described above, the field-effect transistor and the method of manufacturing the same may be applied to a field-effect transistor (FET) of a polycrystalline silicon source / drain, a gate dielectric film and a polycrystalline silicon source / drain are shielded by a silicon oxide It is possible to realize a manufacturing method capable of increasing the electric field effect of the transistor by suppressing possible reaction or current leakage between the two materials.
Claims (10)
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| KR1019960034661A KR19980015364A (en) | 1996-08-21 | 1996-08-21 | Field effect transistor and manufacturing method thereof |
| JP9231845A JP3013166B2 (en) | 1996-08-21 | 1997-08-13 | Field effect transistor and method of manufacturing the same |
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Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7741673B2 (en) | 2006-12-13 | 2010-06-22 | Samsung Electronics Co., Ltd. | Floating body memory and method of fabricating the same |
| US7851859B2 (en) | 2006-11-01 | 2010-12-14 | Samsung Electronics Co., Ltd. | Single transistor memory device having source and drain insulating regions and method of fabricating the same |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| KR100590580B1 (en) * | 2005-03-21 | 2006-06-19 | 삼성전자주식회사 | Method of manufacturing patterned ferroelectric media |
-
1996
- 1996-08-21 KR KR1019960034661A patent/KR19980015364A/en not_active Ceased
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Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7851859B2 (en) | 2006-11-01 | 2010-12-14 | Samsung Electronics Co., Ltd. | Single transistor memory device having source and drain insulating regions and method of fabricating the same |
| US7741673B2 (en) | 2006-12-13 | 2010-06-22 | Samsung Electronics Co., Ltd. | Floating body memory and method of fabricating the same |
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| JPH10321739A (en) | 1998-12-04 |
| JP3013166B2 (en) | 2000-02-28 |
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