O2 플라즈마시에 유기물 제거는 어떻게

안녕하세요!

저는 공기청정에 대해 관심이 많은 학생입니다.
검색중에 광플라즈마(Photoplasma)를 이용한 공기 청정,살균 및 탈취 라는 것을 보았습니다.

제가 아는 상식으로는 Glow, Arc, Microwave discharge 등의 방법을 플라즈마를 발생 시킬 수 있는것으로 아는데
단지 광촉매와 UV를 이용 한 것같은데...
아래의 방식으로 플라즈마를 만들 수 있는지 그리고 플라즈마 상태 라고 할 수 있는것인지 궁금합니다.

감사합니다.

-------아래-------
광화학 원리를 이용한 저온 플라즈마와 그리고 광이온화는 공기와 표면에서 유기화합물과 생물학적 오염물질을 동시에 제거할 수 있다고 합니다.
이 방법은 전세계 과학계에서 충분히 연구되었고 이미 입증되었습니다.

우수한 실내공기질을 지속적으로 보증하기 위한 최상의 방법은 “실시간”으로 실제적으로 이 기술을 실내에 제공함으로써 상호작용에 의한 시너지를 만들어 내는 것입니다.
이러한 시너지 효과를 보증하기 위해서 건물 내 전체로 적당한 온도와 습기를 골고루 분포시키는 말하자면, 사람의 "심장과 허파"와 같은 역할을 하는 중앙집중식 냉난방 환기장치(HVAC System)을 적극적으로 활용하는 것입니다.
광화학은 빛 에너지의 노출이 기인한 어떤 물질 내에서 일어나는 화학반응이자 변화입니다.

이 반응 과정은 일반적으로 자외선 파장 범위 내에서 쏟아져 나오는 광자(Photon)의 활용을 반드시 요구합니다.
자외선 방사는 오염 물질의 화학적 결합을 자극하거나 그 분자의 결합을 절단하기에 충분할 정도의 광 반응을 유도해야 합니다.
강렬한 자외선 방사는 살균 소독 목적에 매우 유용합니다.
이것을 이용하기 위해서는 자외선의 근원에 대한 물리적인 요소로서 기본적으로 충분히 강력하고 높은 강도의 광에너지(파장)를 반드시 요구합니다.
충분한 광에너지가 존재하고 있을 때, 자외선 빛은 유기화합 물질의 파괴에 특히 유용합니다.

특히 자외선 빛은 유기체 분자의 전자 사이의 결합을 100-280나노미터 사이의 강력한 에너지로서 붕괴시킬 수 있습니다. 더욱 더 짧은 단 파장일수록 더 많은 광에너지가 발생되고 분자의 결합을 깨뜨립니다.
모든 유기체 물질은 일정한 파장 범위 내에서 광분해 할 수 있습니다.

100-280 나노미터 대역 내의 LJV 파장은 유기체 화합물질의 전자의 결합을 붕괴시키는 것뿐만 아니라 저온 플라즈마 형성을 개시합니다. 일반적으로 방전 플라즈마는 라디오 주파수 에너지(RF)로 가스체에 자기장을 갖게 합니다. 그러나 우리 경우는 자외선 광 파장으로 발생한 에너지를 가지고 가스체에 자기장을 갖도록 만들었습니다.

우리가 만든 높은 에너지를 가진 가스체 상태의 광플라즈마는 높은 에너지를 가진 가스체 상태로 더욱 강화되어 있기 때문에 높은 반응과 들뜬(흥분 상태)상태의 전자와 분자 그리고 이온화된 가스체와 자유로운 전자들을 만들어 냅니다.
이러한 정화제들은 유기체 오염물질들을 그 어떤 수단보다 확실하게 파괴시킬 수 있습니다.

기본적으로 파괴의 메커니즘은 산소 분자의 광학적 해리를 이끌어 내어 산소 원자와 단일 산소 분자 그리고 활성화된 산소와 같은 매우 높은 산화력을 지닌 산소 종의 생성과 밀접하게 관련되어 있습니다.
이러한 산소 플라즈마 정화제들은 오염물질과 상호 작용하고, 대부분 휘발되어 이산화탄소(CO2)와 물(H2O)로 오염물질들을 무해화 하면서 안전하게 환원됩니다.

LJV 방사는 또한 추가적으로 자유 래디컬을 발생할 수 있도록 유기체 물질의 분자를 결합하는 전자의 분출을 이끌어 냅니다. 이렇게 생성된 래디컬은 산소와 반응하여 과산화수소 이온을 만들어 낼 수 있습니다.
과산화수소의 산화 반응은 유기 화합물을 더욱 더 강력하게 산화하도록 유도하고, 연쇄 반응을 촉진시킵니다.
산화 반응 후 남은 수소(H) 이온은 다시 주위의 수증기(H2O)와 결합하여 추가적으로 매우 강력한 산화 물질인 새로운 수산기(OH)를 만들어 냅니다.

이 수산기(OH)는 쉽게 분해되지 않으면서 1개의 전자를 더 가진 매우 강력한 산화력을 지니고 있습니다.
수산기(OH)는 인체에 유해한 유기 물질로부터 수소 원자(H)를 빼앗아 수분(H2O)으로 환원하고, 결국은 남은 탄소 이온(C)마저 붕괴시키기 때문에 유기 오염물질의 파괴에 매우 효과적입니다.

이때 유기 분자의 붕괴 과정에서 남은 수소 이온(H)은 더욱 더 높은 산화력을 잠재한 채 화학적으로 더욱 더 강력한 수산기(OH)를 유기 오염물질이 존재하는 한 지속적으로 이끌어 낼 수 있습니다. 이러한 전체적인 반응 과정은 연쇄 반응으로 나타나고, 수산기 (OH)로 인해서 오염물질이 붕괴되고, 새로운 수산기(OH)가 형성됨으로써 실내 공기 중의 유기 오염물질을 지속적으로 파괴시킵니다.

분자 상태의 오염물질이 강력한 광 에너지를 받으면 분자 주위의 전자들이 분출되면서 광전자 효과가 만들어 집니다.
광에너지를 가진 강력한 자외선 빛의 방사로 인해서 광전자는 “광전자 증폭기관” 이라고 부르는 장치에 의해 더욱 더 그 힘이 강화됩니다.
이러한 광전자 증폭 기관은 우리의 기술에 포함되어 있습니다.
이때 공기 입자들이 전기적으로 대전되면서 0.001미크론 크기의 극히 미세한 입자까지 제거할 수 있습니다.

이 현상은 분출된 전자가 다른 주위 물질에 충돌하여 이온화하는 복합적인 원인들로 인해 일어난다는 것을 알게 되었습니다.
예를 들면, 광전자 효과에서 광자는 단지 한 개씩만 서로 그 영향을 줄뿐이며, 방출된 다량의 전자가 만들어낸 전리 이온들은 그 전자를 다량으로 만들어 낸 결과입니다.
자외선 빛과 플라즈마의 결합은 모든 물질의 표면에서 오염물질을 제거하는데 대단히 유용한 것으로 이미 공식적으로 발표되었습니다.

하나의 예로서 비교한다면 코로나 방전으로 발생한 오존 만으로 물질의 표면에서 생물학적 오염물질을 제거하려면 무려 10시간 이상이 걸립니다.
만약 254 나노미터의 파장의 강력한 살균력을 지닌 UVC 자외선 빛만으로 똑같은 결과를 얻으려면 무려 1시간 이상 걸립니다.
코로나 방전으로 만들어낸 오존과 UVC 자외선을 함께 결합하여 같은 결과를 얻으려면 최소한 1분 30초(90초) 정도가 걸립니다.
하지만 더욱 더 넓은 공간을 정화하면서 더욱 더 강력한 자외선 파장을 플라즈마와 함께 결합된다면 똑같은 결과를 성취하는데 불과 20초 만에 깨끗이 해결할 수 있습니다.

KR101225238B1 - 플라즈마 세정 방법 - Google Patents

플라즈마 세정 방법 Download PDF

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Publication numberKR101225238B1 KR101225238B1 KR1020110014961A KR20110014961A KR101225238B1 KR 101225238 B1 KR101225238 B1 KR 101225238B1 KR 1020110014961 A KR1020110014961 A KR 1020110014961A KR 20110014961 A KR20110014961 A KR 20110014961A KR 101225238 B1 KR101225238 B1 KR 101225238B1AuthorityKRSouth KoreaPrior art keywordsgasplasmasubstratesiliconsemiconductor elementPrior art date2010-02-22Application numberKR1020110014961AOther languages English (en) Other versions KR20110096499A (koInventor마사유끼 후꾸다나오야 무라까미Original Assignee가부시끼가이샤 히다찌 하이테크 인스트루먼츠Priority 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.)2010-02-22Filing date2011-02-21Publication date2013-01-22 2010-02-22 Priority to JPJP-P-2010-036731 priority Critical 2010-02-22 Priority to JP2010036731 priority 2011-01-20 Priority to JPJP-P-2011-010202 priority 2011-01-20 Priority to JP2011010202A priority patent/JP2011189338A/ja 2011-02-21 Application filed by 가부시끼가이샤 히다찌 하이테크 인스트루먼츠 filed Critical 가부시끼가이샤 히다찌 하이테크 인스트루먼츠 2011-08-30 Publication of KR20110096499A publication Critical patent/KR20110096499A/ko 2013-01-22 Application granted granted Critical 2013-01-22 Publication of KR101225238B1 publication Critical patent/KR101225238B1/ko

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  • 210000002381 Plasma Anatomy 0.000 title claims abstract description 57
  • 238000004140 cleaning Methods 0.000 title claims abstract description 39
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  • XKRFYHLGVUSROY-UHFFFAOYSA-N argon Chemical compound data:image/svg+xml;base64,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 data:image/svg+xml;base64,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 [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 claims abstract description 58
  • SFZCNBIFKDRMGX-UHFFFAOYSA-N Sulfur hexafluoride Chemical compound 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FS(F)(F)(F)(F)F SFZCNBIFKDRMGX-UHFFFAOYSA-N 0.000 claims abstract description 32
  • 239000000853 adhesive Substances 0.000 claims abstract description 32
  • 239000004065 semiconductor Substances 0.000 claims abstract description 32
  • 229960000909 sulfur hexafluoride Drugs 0.000 claims abstract description 32
  • 229910052786 argon Inorganic materials 0.000 claims abstract description 29
  • 229910052710 silicon Inorganic materials 0.000 claims abstract description 27
  • 239000010703 silicon Substances 0.000 claims abstract description 27
  • 230000001070 adhesive Effects 0.000 claims abstract description 26
  • NINIDFKCEFEMDL-UHFFFAOYSA-N sulfur Chemical compound 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[S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 24
  • 239000011593 sulfur Substances 0.000 claims abstract description 24
  • 229910052717 sulfur Inorganic materials 0.000 claims abstract description 24
  • 125000005373 siloxane group Chemical group 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[SiH2](O*)* 0.000 claims abstract description 23
  • 239000011737 fluorine Substances 0.000 claims abstract description 11
  • 229910052731 fluorine Inorganic materials 0.000 claims abstract description 11
  • YCKRFDGAMUMZLT-UHFFFAOYSA-N fluorine atom Chemical compound 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[F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims abstract description 11
  • XUIMIQQOPSSXEZ-UHFFFAOYSA-N silicon Chemical compound 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[Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 25
  • 229910001882 dioxygen Inorganic materials 0.000 claims description 14
  • 238000007747 plating Methods 0.000 claims description 12
  • BQCADISMDOOEFD-UHFFFAOYSA-N silver Chemical compound 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[Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims description 9
  • 229910052709 silver Inorganic materials 0.000 claims description 9
  • 239000004332 silver Substances 0.000 claims description 9
  • 229920002994 synthetic fiber Polymers 0.000 claims description 9
  • 238000007872 degassing Methods 0.000 claims description 6
  • 239000012495 reaction gas Substances 0.000 claims description 6
  • -1 Then Chemical compound 0.000 claims 1
  • 229920001296 polysiloxane Polymers 0.000 abstract description 12
  • ABTOQLMXBSRXSM-UHFFFAOYSA-N Silicon tetrafluoride Chemical compound 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F[Si](F)(F)F ABTOQLMXBSRXSM-UHFFFAOYSA-N 0.000 description 12
  • 238000000034 method Methods 0.000 description 8
  • XUARKZBEFFVFRG-UHFFFAOYSA-N Silver sulfide Chemical compound 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[S-2].[Ag+].[Ag+] XUARKZBEFFVFRG-UHFFFAOYSA-N 0.000 description 7
  • 229910052946 acanthite Inorganic materials 0.000 description 7
  • 229940056910 silver sulfide Drugs 0.000 description 7
  • OKTJSMMVPCPJKN-UHFFFAOYSA-N carbon Chemical compound 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[C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 6
  • 229910052799 carbon Inorganic materials 0.000 description 6
  • 238000010438 heat treatment Methods 0.000 description 6
  • 238000001020 plasma etching Methods 0.000 description 6
  • 238000004544 sputter deposition Methods 0.000 description 6
  • 239000000356 contaminant Substances 0.000 description 5
  • TXEYQDLBPFQVAA-UHFFFAOYSA-N Tetrafluoromethane Chemical compound 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  • CURLTUGMZLYLDI-UHFFFAOYSA-N carbon dioxide Chemical compound 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  • 229910002092 carbon dioxide Inorganic materials 0.000 description 3
  • 239000001569 carbon dioxide Substances 0.000 description 3
  • 238000010586 diagram Methods 0.000 description 3
  • 239000012212 insulator Substances 0.000 description 3
  • 230000004048 modification Effects 0.000 description 3
  • 238000006011 modification reaction Methods 0.000 description 3
  • 229920001187 thermosetting polymer Polymers 0.000 description 3
  • 230000002411 adverse Effects 0.000 description 2
  • 238000006243 chemical reaction Methods 0.000 description 2
  • 229920001577 copolymer Polymers 0.000 description 2
  • 238000002845 discoloration Methods 0.000 description 2
  • 150000002431 hydrogen Chemical class 0.000 description 2
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  • 229920000642 polymer Polymers 0.000 description 2
  • RAHZWNYVWXNFOC-UHFFFAOYSA-N sulphur dioxide Chemical compound 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[Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
  • 229910052737 gold Inorganic materials 0.000 description 1
  • 239000010931 gold Substances 0.000 description 1
  • 238000005286 illumination Methods 0.000 description 1
  • 239000000463 material Substances 0.000 description 1
  • 229910052763 palladium Inorganic materials 0.000 description 1
  • OAICVXFJPJFONN-UHFFFAOYSA-N phosphorus Chemical compound 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[P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
  • 229910052698 phosphorus Inorganic materials 0.000 description 1
  • 239000011574 phosphorus Substances 0.000 description 1
  • 238000009832 plasma treatment Methods 0.000 description 1
  • 239000000376 reactant Substances 0.000 description 1

Images

Classifications

    • HELECTRICITY
    • H05ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
    • H05KPRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
    • H05K3/00Apparatus or processes for manufacturing printed circuits
    • H05K3/22Secondary treatment of printed circuits
    • H05K3/26Cleaning or polishing of the conductive pattern
    • HELECTRICITY
    • H05ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
    • H05HPLASMA TECHNIQUE; PRODUCTION OF ACCELERATED ELECTRICALLY-CHARGED PARTICLES OR OF NEUTRONS; PRODUCTION OR ACCELERATION OF NEUTRAL MOLECULAR OR ATOMIC BEAMS
    • H05H1/00Generating plasma; Handling plasma
    • H05H1/24Generating plasma
    • H05H1/46Generating plasma using applied electromagnetic fields, e.g. high frequency or microwave energy
    • H05H1/4645Radiofrequency discharges
    • HELECTRICITY
    • H05ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
    • H05KPRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
    • H05K3/00Apparatus or processes for manufacturing printed circuits
    • H05K3/0011Working of insulating substrates or insulating layers
    • H05K3/0055After-treatment, e.g. cleaning or desmearing of holes
    • HELECTRICITY
    • H05ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
    • H05KPRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
    • H05K2203/00Indexing scheme relating to apparatus or processes for manufacturing printed circuits covered by H05K3/00
    • H05K2203/09Treatments involving charged particles
    • H05K2203/095Plasma, e.g. for treating a substrate to improve adhesion with a conductor or for cleaning holes

Abstract

본 발명은 열 경화형 실리콘계 접착제를 개재하여 반도체 소자가 장착된 기판을 플라즈마 처리하고, 접착제 중에 포함된 실록산 성분을 제거하여, 그 후 신뢰성이 높은 와이어 본딩 등을 행할 수 있도록 하는 것이다.
또한, 진공 챔버(1)을 소정의 진공 상태로 하여, 고주파 전원(10)으로부터의 고주파 전압을 하부 전극(3)에 고주파 전압을 인가한다. 또한, 개폐 밸브(23)을 개방하고, 상부 전극(2)와 하부 전극(3) 사이에 육불화황 가스를 공급하여 플라즈마화한다. 그렇게 하면, 육불화황 가스의 불소가 실리콘계 접착제(7) 중의 규소와 합체하고, 이 규소는 진공 통로(6)을 통하여 장치 외부로 배출된다. 이 플라즈마 세정을 60초간 행한 후, 5초 경과 후에 상부 전극(2)와 하부 전극(3) 사이에 아르곤 가스를 공급하여 플라즈마화한다. 그렇게 하면, 아르곤 가스의 아르곤이 육불화황 가스 중의 황과 결합하고, 이 황은 진공 통로(6)을 통하여 장치 외부로 배출된다.

Description

플라즈마 세정 방법{PLASMA CLEANING METHOD}

본 발명은 챔버 내에 한 쌍의 전극을 배치하여, 진공 상태가 된 챔버 내에 기판을 수납하여, 플라즈마 반응성 가스를 공급함과 동시에, 한쪽의 상기 전극에 고주파 전원에 의해 고주파 전압을 인가하여 상기 반응성 가스를 플라즈마화하여 상기 인쇄 기판을 세정하고, 이 세정한 후의 플라즈마화된 반응성 가스를 장치 밖으로 배출하는 플라즈마 세정 방법에 관한 것이다. 상술하면, 상기 기판은 열 경화형 실리콘계 접착제를 개재하여 반도체 소자가 장착된 것이고, 상기 접착제 중에 포함된 실록산을 제거 세정하는 플라즈마 세정 방법에 관한 것이다.

이 종류의 플라즈마 세정 방법은, 예를 들면 특허문헌 1 등에 개시되어 있지만, 열 경화형 실리콘계 접착제를 개재하여 반도체 소자가 장착된 기판에 대해서는 상기 기판을 경화로(가열로) 내에 넣어 상기 접착제를 경화시킨다.

일본 특허 공개 제2007-123370호 공보

그러나, 접착제를 열 경화시킬 때에 기판의 전극부나 반도체 소자의 본딩 패드부의 표면에 이 접착제 중에 포함된 실록산 성분이 쌓이게 된다. 그러면, 이 실록산 성분은 절연체이기 때문에, 그 후에 행해지는 와이어 본딩 또는 몰드의 신뢰성을 손상시킨다는 문제점이 발생한다.

따라서, 본 발명은 이 열 경화형 실리콘계 접착제를 개재하여 반도체 소자가 장착된 기판을 가열로 내에 넣어 상기 접착제를 경화시킬 때에, 이 접착제 중에 포함된 실록산 성분이 기판 등에 쌓이더라도 실록산 성분을 제거하여, 그 후 신뢰성이 높은 와이어 본딩 또는 몰드를 행할 수 있도록 하는 것을 목적으로 한다. 또한, 상기 반도체 소자 또는 이 반도체 소자가 장착된 기판에 부착된 황도 제거하여, 반도체 소자에 대한 악영향을 방지하는 것도 목적으로 한다.

이 때문에, 제1 발명은 챔버 내에 한 쌍의 전극을 배치하고, 진공 상태가 된 챔버 내에 실리콘계 접착제를 개재하여 반도체 소자가 장착된 기판을 수납하여, 플라즈마 반응성 가스를 공급함과 동시에, 상기 한 쌍의 전극에 고주파 전원에 의해 고주파 전압을 인가하여 상기 반응성 가스를 플라즈마화하여 상기 기판을 세정하고, 이 세정한 후의 플라즈마화된 반응성 가스를 장치 밖으로 배출하는 플라즈마 세정 방법이며,

처음에, 상기 반응성 가스로서 육불화황 가스를 사용하고, 육불화황 가스의 불소가 실리콘계 접착제에 포함되어 상기 반도체 소자의 표면에 부착된 실록산 중의 규소와 합체하여, 이 규소를 제거하고,

이어서, 상기 반응성 가스로서 아르곤 가스를 사용하고, 이 아르곤 가스 중의 아르곤이 상기 반도체 소자 또는 이 반도체 소자가 장착된 기판에 부착된 황을 제거하는 것을 특징으로 한다.

제2 발명은 챔버 내에 한 쌍의 전극을 배치하고, 진공 상태가 된 챔버 내에 전극부가 은 도금으로 제작되고 실리콘계 접착제를 개재하여 반도체 소자가 장착된 기판을 수납하여, 플라즈마 반응성 가스를 공급함과 동시에, 상기 한 쌍의 전극에 고주파 전원에 의해 고주파 전압을 인가하여 상기 반응성 가스를 플라즈마화하여 상기 기판을 세정하고, 이 세정한 후의 플라즈마화된 반응성 가스를 장치 밖으로 배출하는 플라즈마 세정 방법이며,

처음에, 상기 반응성 가스로서 육불화황 가스 및 산소 가스를 사용하고, 육불화황 가스의 불소가 실리콘계 접착제에 포함되어 상기 반도체 소자의 표면에 부착된 실록산 중의 규소와 합체하여 생성된 규소를 포함하는 합성 물질을 제거함과 동시에, 육불화황 가스의 황(S)이 산소 가스(O2)와 합체하여 생성된 황을 포함하는 합성 물질을 제거하고,

이어서, 상기 반응성 가스로서 아르곤 가스를 사용하고, 이 아르곤 가스 중의 아르곤이 상기 반도체 소자 또는 이 반도체 소자가 장착된 기판에 부착된 황을 포함하는 합성 물질을 제거하는 것을 특징으로 한다.

또한, 제3 발명은 제1 또는 제2 발명에 있어서, 상기 챔버의 탈기를 플라즈마 반응 가스를 공급하지 않고 규소 제거 후에 아르곤 가스의 사용 전에 하는 것을 특징으로 한다.

본 발명에 따르면, 열 경화형 실리콘계 접착제를 개재하여 반도체 소자가 장착된 기판을 가열로 내에 넣어 상기 접착제를 경화시킬 때에, 이 접착제 중에 포함된 실록산 성분이 기판 등에 쌓이더라도 실록산 성분을 제거하여, 그 후 신뢰성이 높은 와이어 본딩 또는 몰드를 행할 수 있도록 할 수 있다. 또한, 황을 제거할 수 있기 때문에, 반도체 소자에 대한 악영향을 방지할 수 있다.

또한, 기판의 전극부가 은 도금으로 제작된 기판에 대해서는, 처음에 반응성 가스로서 육불화황 가스를 사용했을 때에 은과 황이 반응하여 황화은이 발생하는 경우가 있었지만, 이 황화은의 발생을 방지하여 도금의 변색의 발생을 방지할 수 있다.

도 1은 플라즈마 세정 장치의 개략도이다.
도 2는 기판의 정면도이다.
도 3은 플라즈마 세정에 관한 레시피 설정 화면을 도시한 도면이다.
도 4는 플라즈마 세정 처리의 레시피 번호를 선택하는 화면을 도시한 도면이다.

이하, 도 1을 참조하면서, 본 발명의 실시 형태에 관한 플라즈마 세정 장치에 대하여 설명한다. 1은 진공 챔버로, 이 진공 챔버(1) 내에는 한 쌍의 평행한 상부 전극(2) 및 하부 전극(3)이 배치된다. 그리고, 이 진공 챔버(1)은 진공 통로(6) 중에 설치된 개폐 밸브(4)를 통해 진공 펌프(5)에 의해 소정의 진공 상태가 된다.

그리고, 그랜드 전위에 접속된 상기 상부 전극(2)를 관통하고, 후술하는 플라즈마 반응성 가스를 공급 통로(20)을 통해, 상부 전극(2)와 하부 전극(3) 사이에 공급한다. 이 하부 전극(3) 상에, 전극부(9)를 구비한 세정해야할 기판(PB)가 배치된다. 도 2에 나타낸 바와 같이, 이 기판(PB) 상에는 열 경화형 실리콘계 접착제(7)을 개재하여 반도체 소자인 LED(Light Emitting Diode; 발광 다이오드) 칩(8)이 장착된다. 또한, 이 기판(PB)는 세라믹 기판이지만, 리드 프레임이나 그 밖의 기판일 수도 있다.

10은, 접지에 접속된 고주파 전원으로, 상기 하부 전극(3)에 자동 정합기(11)을 통해 고주파 전압을 인가하여, 상기 플라즈마 반응성 가스를 플라즈마화시키는 것이다. 그리고, 생성된 플라즈마 중의 양이온이 상기 하부 전극(3) 상의 기판(PB)에 충돌함으로써, 이 기판(PB)의 표면이나 LED칩(8) 표면 등을 스퍼터링하여, 후술하는 오염 물질을 제거, 세정한다.

13은, 마이크로 컴퓨터 등으로 구성되는 제어 장치로, 상기 고주파 전원(10), 그 밖의 구동원 등을 제어하여, 본 플라즈마 세정 장치를 통괄 제어한다. 14는 각종 데이터를 저장하는 기억 장치, 15는 인터페이스(17)을 통해 제어 장치(13)에 접속되는 표시 장치로서의 모니터, 이 모니터(15)에는 입력 수단으로서의 여러 가지 터치 패널 스위치(16)이 설치되고, 작업자가 터치 패널 스위치(16)을 조작함으로써, 여러 가지 설정을 행할 수 있다.

그리고, 제어 장치(13)은 인터페이스(17) 및 구동 회로(18)을 통해 상기 개폐 밸브(4), 진공 펌프(5), 가스 봄베(19)로부터 아르곤 가스(Ar 가스)가 공급되는 공급 통로(20) 중에 설치된 개폐 밸브(21), 가스 봄베(22)로부터 육불화황 가스(SF6)가 공급되는 공급 통로(20) 중에 설치된 개폐 밸브(23) 등의 구동을 제어한다. 24, 25는 흐르는 반응성 가스의 양을 계측하는 유량계로, 상기 각 공급 통로(20)에, 가스 봄베(19)와 개폐 밸브(21) 사이, 가스 봄베(22)와 개폐 밸브(23) 사이에 배치된다.

여기서, 열 경화형 실리콘계 접착제(7)을 개재하여 LED칩(8)이 장착된 상기 기판(PB)는 경화로(가열로) 내에 수납되고, 경화된 실리콘계 접착제(7)에 의해 LED칩(8)은 기판(PB) 상에 고정된다. 이 경화의 때에, 기판(PB)의 전극부(9)나 LED칩(8)의 본딩 패드부의 표면에 이 접착제 중에 포함된 실록산 성분이 쌓이게 되는 것이다. 그러면, 이 실록산 성분은 절연체이기 때문에, 그 후에 행해지는 LED칩(8)과 기판(PB)의 전극부(9)의 접속을 위한 와이어 본딩의 신뢰성을 손상시킨다는 문제점이 발생한다. 따라서, 이 플라즈마 세정 장치로써 실록산 성분을 제거하는 것이며, 본 발명의 제1 실시 형태의 세정 처리에 관하여 이하에 설명한다.

우선, 모니터(15)에 터치 패널 스위치(16)의 가압 조작에 의해, 도 3에 나타낸 바와 같은 플라즈마 세정 처리의 레시피 설정 화면을 표시시키고, 입력키로서의 숫자키 스위치부를 표시시키고, 각종 데이터를 입력하여 레시피를 설정한다. 즉, 플라즈마 에칭을 행하는 레시피 번호 「1」의 제1 스텝으로서, 공급하는 아르곤 가스(「Ar」라 표시함)를 「0」으로서, 공급하는 육불화황 가스(「SF6」라 표시함)를 「20(1분간 당 20 cc의 의미)」로 하고, 플라즈마 세정할 때의 개시 압력을 「20(Pa)」로 하고, RF 전원 출력 파워를 「600(W)」로 하고, 플라즈마 처리 시간을 「60(초간)」으로 하고, RF 방식을 RIE(Reactive Ion Etching; 반응성 이온 에칭) 처리로 하고, 스퍼터링을 행하고, 그 후 제2 스텝까지의 간격을 「0005(5초간)」라고 입력한다.

또한, 제2 스텝으로서, 공급하는 아르곤 가스(「Ar」라 표시함)를 「5(1분간 당 5 cc의 의미)」로서, 공급하는 육불화황 가스(「SF6」라 표시함)를 「0」으로 하고, 플라즈마 세정할 때의 개시 압력을 「20(Pa)」로 하고, RF 전원 출력 파워를 「600(W)」로 하고, RF 방식을 RIE(Reactive Ion Etching) 처리로 하고, 플라즈마 처리 시간을 「0020(20초간)」이라고 입력한다.

이하 동일하게, 레시피 번호 「2」, 「3」의 제1 스텝 및 제2 스텝의 필요 사항을 입력하지만, 여기서는 생략한다. 이와 같이 하여, 레시피 번호 「1」, 「2」, 「3」의 필요 사항을 입력한 후에, 터치 패널 스위치(16)의 데이터 갱신 스위치부(16A)를 압압 조작하면, 제어 장치(13)은 처음에 설정 입력거나 또는 갱신 입력한 레시피 데이터를 기억 장치(14)에 저장시키고, 또한 입력 종료 스위치부(16A)를 압압 조작하면, 이 레시피 설정 화면을 폐쇄하도록 제어한다.

이상의 구성으로부터, 이하 동작에 관하여 설명한다. 우선, 설정된 플라즈마 세정 처리의 레시피를 선택하기 위해 모니터(15)에, 도 4에 나타낸 선택 화면을 표시시키고, 레시피 번호 「1」을 선택하기 위해, 터치 패널 스위치(16)의 대응하는 체크·박스 스위치부(16C)를 압압 조작하여 체크·마크(レ)를 붙인다. 그리고, 운전 개시 스위치(도시 생략)를 조작하여, 본 플라즈마 세정 장치의 운전을 시작시킨다.

이렇게 하면, 처음에 제어 장치(13)은 개폐 밸브(4)를 개방하여 진공 펌프(5)를 구동시키고, 진공 챔버(1)을 소정의 진공 상태로 하여, 고주파 전원(10)으로부터의 고주파 전압을 하부 전극(3)에 자동 정합기(11)을 통해 고주파 전압을 인가하도록 제어한다. 또한, 개폐 밸브(23)을 개방하고, 상부 전극(2)를 관통하여, 이 상부 전극(2)와 하부 전극(3) 사이에 제1 스텝의 플라즈마 반응성 가스인 육불화황 가스를 가스 봄베(22)로부터 유량계 25로 계측하면서 1분간 당 20 cc분 공급하여 플라즈마화한다. 이 경우, 육불화황 가스가 소정의 유량으로 진공 챔버(1) 내에 공급되고, 소정의 진공압을 유지하도록 개폐 밸브(4)를 개방하여, 항상 배기하게 되어 대략 일정 농도의 육불화황 가스가 진공 챔버(1) 내를 채우고 있다.

그리고, 기판(PB)의 표면 및 LED칩(8) 표면 등을 에칭하여, 오염 물질을 제거, 세정한다. 즉, 기판(PB)를 경화로(가열로) 안에 수납하고, 실리콘계 접착제(7)을 경화하여, LED칩(8)을 기판(PB) 상에 고정하지만, 이 경화의 때에, 기판(PB)의 전극부(9)나 LED칩(8)의 본딩 패드부의 표면에 상기 접착제(7) 중에 포함된 실록산 성분이 쌓이지만, 경화로에서 취출한 LED칩(8)을 고정한 기판(PB)를 진공 챔버(1) 내에 넣고, 상기 반응성 가스로서 육불화황 가스(SF6)를 사용하여, 육불화황 가스의 불소(F)가 실록산 성분 중의 규소(Si)와 합체하여 불화규소(SiF)를 생성하고, 이 불화규소는 진공 통로(6)을 통해 장치 외부로 배출된다. 이 경우, 육불화황 가스의 공급과, 규소와 불소의 합성 물질(불화규소)의 진공 통로(6)을 통한 배출과는 평행하게 항상 행해진다.

레시피 번호 「1」의 세정 처리에서는 이러한 육불화황 가스를 공급하면서, 플라즈마화하여 세정하고 장치 외부로 배출하는 플라즈마 세정 처리의 제1 스텝은 60초간 행해지고, 이 제1 스텝 종료에서부터 5초 경과하면, 다음에 제2 스텝의 플라즈마 세정 처리가 20초간 행해지게 된다.

그리고, 육불화황 가스 중의 불소가 규소와 합체하여 가스상의 불화규소(SiF)를 생성하고, 황(S)은 남아서 LED칩(8)을 포함시킨 반도체 소자 및 기판(PB) 등에 부착된 상태가 된다.

따라서, 처음에 개폐 밸브(23)을 폐쇄하여 제1 스텝이 종료되고 나서 5초간, 진공 챔버(1) 내의 제1 스텝에서 사용한 반응성 가스를 포함하는 각종 가스를 진공 통로(6)을 통해 장치 외부로 배출시킨다(개폐 밸브(4)는 열린 상태). 즉, 플라즈마 반응 가스를 공급하지 않고 상기 진공 챔버(1)을 탈기한다. 그리고, 이 탈기를 5초간 행하고, 이 5초 경과 후에 개폐 밸브(21)을 개방하여, 상부 전극(2)와 하부 전극(3) 사이에 제2 스텝의 플라즈마 반응성 가스인 아르곤 가스(Ar)를 가스 봄베(19)로부터 유량계(24)로 계측하면서, 1분간 당 5 cc분 공급하여 플라즈마화한다.

그리고, 생성된 플라즈마 중의 양이온이 상기 하부 전극(3) 상의 기판(PB)에 충돌함으로써, 기판(PB)의 표면 및 LED칩(8) 표면 등을 스퍼터링하여, 오염 물질을 제거, 세정한다. 즉, 아르곤 가스의 아르곤(Ar)이 LED칩(8)을 포함시킨 반도체 소자 및 기판(PB) 표면 등에 부착되어 있는 황 및 그 밖의 유기물 성분 등(탄소, 산소 등)을 제거하고, 제거된 황 및 그 밖의 유기물 성분 등이 진공 통로(6)을 통해 장치 외부로 배출된다(개폐 밸브(4)는 열린 상태). 그리고, 이러한 플라즈마 처리의 제2 스텝은 20초간 행해진다. 따라서, 이 제2 스텝에서는 특히 LED칩(8)에 악영향을 제공하는 황을 제거할 수 있다.

이상과 같이, 기판(PB)를 경화로(가열로) 내에 수납하여 실리콘계 접착제(7)을 경화하여, LED칩(8)을 기판(PB) 상에 고정하지만, 이 경화의 때에, 기판(PB)의 전극부(9)나 LED칩(8)의 본딩 패드부의 표면에 상기 접착제(7) 중에 포함된 실록산 성분이 쌓이게 된다. 그러면, 이 실록산 성분은 절연체이기 때문에, 종래에는 그 후에 행해지는 와이어 본딩의 신뢰성을 손상시키는 문제점이 발생하였지만, 본 발명은 실록산 성분을 제거할 수 있어서, 신뢰성이 높은 와이어 본딩을 행할 수 있다.

또한, 제1 스텝의 육불화황 가스의 공급으로부터 제2 스텝의 아르곤 가스의 공급에의 변환의 때에는 반드시 간격을 둘 필요는 없다. 즉, 제1 스텝 후에, 탈기만 하는 기간을 두지 않고서, 제2 스텝을 이행할 수 있다.

이상과 같은 세정 처리의 제1 실시 형태는 기판(PB)의 전극부(9)가 은 도금이나, 금 도금, 팔라듐 도금 등의 도금으로 제작된 경우에도 적용할 수 있다.

그러나, 기판(PB)의 전극부(9)가 은 도금으로 제작되어 있는 경우에는, 상술한 제1 스텝에서의 육불화황 가스의 사용 시에, 어떻게 해도 황이 기판(PB)에 남아있어서, 이 황과 기판(PB)의 전극부(9)의 은 도금이 반응하여 황화은(AgS)이 약간 생성되기 때문에, 이 황화은에 의해 도금이 변색된다는 문제가 발생하는 경우가 있었다. 이 때문에, LED칩(8)에 의한 조명이 황색빛으로 되는 문제가 발생한다.

따라서, 이 문제를 해소하는 제2 실시 형태에 관하여, 이하에 설명한다. 이 실시 형태에서는 플라즈마 에칭을 행하는 제1 스텝에서, 플라즈마 반응성 가스로서 육불화황 가스(SF6)와 더불어 산소 가스(O2)도 사용한다. 그러면, 육불화황 가스의 불소(F)가 상술한 바와 같은 기판(PB)의 전극부(9)나 LED칩(8)의 본딩 패드부의 표면에 쌓인 실록산 성분 중의 규소(Si)와 합체하여 합성 물질인 가스상의 불화규소(SiF)가 생성됨과 동시에, 육불화황 가스의 황이 산소 가스(O2)와 합체하여 합성 물질인 가스상의 이산화황(SO2)이 생성된다. 따라서, 황과 기판(PB)의 전극부(9)의 은 도금이 반응함으로써 황화은(AgS)이 생성되는 것이 방지되기 때문에, 이 황화은에 의해 도금이 변색되는 것이 방지된다.

또한, 기판(PB) 상의 전극부(9)에 부착되어 있는 그 밖의 유기물 성분인 탄소(C)가 산소 가스(O2)와 합체하여 가스상의 이산화탄소(CO2)가 생성되거나, 수소(H)가 산소 가스(O2)와 합체하여 수증기(H2O)가 생성된다.

그리고, 개폐 밸브(23)을 폐쇄하여 이 제1 스텝이 종료되고 나서 소정 시간, 진공 챔버(1) 내의 제1 스텝에서 사용한 반응성 가스, 및 상술한 각종 가스를 진공 통로(6)을 통해 장치 외부로 배출한다(개폐 밸브(4)는 열린 상태). 즉, 플라즈마 반응 가스를 공급하지 않고 상기 진공 챔버(1)을 탈기한다. 그리고, 이 탈기를 상기 소정 시간 행한다.

이 제1 스텝의 처리를 행하면, 잔사로서 전극부(9)를 포함시킨 기판(PB) 표면이나 LED칩(8)을 포함시킨 반도체 소자 표면에 탄소(C), 산소(O), 수소(H), 황(S), 인(P) 등이 약간 남게 된다.

그리고, 스퍼터링을 행하는 제2 스텝으로서, 상기 소정 시간 경과 후에, 개폐 밸브(21)을 개방하고, 상부 전극(2)와 하부 정극 3 사이에 제2 스텝의 플라즈마 반응성 가스인 아르곤 가스(Ar)를 소정량 공급하여 플라즈마화한다.

그리고, 생성된 플라즈마 중의 양이온이 상기 하부 전극(3) 상의 기판(PB)에 충돌함으로써, 기판(PB)의 표면 및 LED칩(8) 표면 등을 스퍼터링하여, 오염 물질을 제거, 세정한다. 즉, 아르곤 가스의 아르곤(Ar)이 전극부(9)를 포함시킨 기판(PB) 표면이나 LED칩(8)을 포함시킨 반도체 소자 표면 등에 부착되어 있는 황(S), 및 그 밖의 유기물 성분 등(탄소, 산소, 수소 등)을 제거하고, 제거된 황 및 그 밖의 유기물 성분 등이 진공 통로(6)을 통해 장치 외부로 배출된다(개폐 밸브(4)는 열린 상태). 그리고, 이러한 플라즈마 처리의 제2 스텝을 소정 시간 행함으로써, 이 제2 스텝에서는 특히 LED칩(8)에 악영향을 제공하는 황을 완전히 제거할 수 있다.

또한, 이상의 제2 실시 형태에서는 플라즈마 반응성 가스로서 육불화황 가스(SF6)와 산소 가스(O2)를 제1 스텝에서 사용하지만, 황(S)과 산소 가스(O2)는, 모두 남기지 않도록 등량으로 하는 것이 바람직하지만, 황(S)을 전극부(9)를 포함시킨 기판(PB) 표면이나 LED칩(8)을 포함시킨 반도체 소자 표면에 남기지 않기 위해서는, 산소 가스가 약간 많은 쪽이 좋다. 황(S)이 완전히 제거되고, 소량 남은 산소는 표면에 부착되어 있는 유기물 성분인 탄소(C)나 수소(H)와 반응하여, 이 반응물인 이산화탄소(CO2) 및 수증기(H2O)가 배출됨으로써 제거된다.

또한, 상기 제2 실시 형태에서는 플라즈마 반응성 가스로서 육불화황 가스(SF6)와 산소 가스(O2)를 제1 스텝에서 사용하였지만, 사불화탄소 가스(CF4)와 산소 가스(O2)를 사용할 수도 있다.

이 경우, 사불화탄소 가스(CF4)의 불소(F)가 상술한 바와 같은 기판(PB)의 전극부(9)나 LED칩(8)의 본딩 패드부의 표면에 쌓인 실록산 성분 중의 규소(Si)와 합체하여 합성 물질인 가스상의 불화규소(SiF)가 생성됨과 동시에, 사불화탄소가스(CF4)의 탄소(C)가 산소 가스(O2)와 합체하여 합성 물질인 가스상의 이산화탄소(CO2)가 생성된다. 그리고, 이 제1 스텝이 종료되고 나서 소정 시간, 진공 챔버(1) 내의 제1 스텝에서 사용한 반응성 가스, 및 상술한 각종 가스를 진공 통로(6)을 통해 장치 외부로 배출한다(개폐 밸브(4)는 열린 상태). 즉, 플라즈마 반응 가스를 공급하지 않고 상기 진공 챔버(1)을 탈기한다. 그리고, 이 탈기를 상기 소정 시간 행한다.

따라서, 사불화탄소 가스(CF4)의 불소(F)가 상기 기판(PB)의 전극부(9)나 LED칩(8)의 본딩 패드부의 표면에 쌓인 실록산 성분 중의 규소(Si)와 합체하여 가스상의 불화규소(SiF)를 생성하고, 이것을 장치 외부로 배출할 수 있다.

다음에, 이 제1 스텝 종료 후의 상기 소정 시간 경과 후에, 제1 및 제2 실시 형태와 동일하게, 상부 전극(2)와 하부 전극(3) 사이에 제2 스텝의 플라즈마 반응성 가스인 아르곤 가스(Ar)를 소정량 공급하여 플라즈마화시킨다. 그리고, 생성된 플라즈마 중의 양이온이 상기 하부 전극(3) 상의 기판(PB)에 충돌함으로써, 기판(PB)의 표면 및 LED칩(8) 표면 등을 스퍼터링하여, 오염 물질을 제거, 세정하여, 이 제2 스텝의 종료 후에, 소정 시간, 진공 챔버(1) 내의 제1 스텝에서 사용한 반응성 가스, 및 상술한 각종 가스를 진공 통로(6)을 통해 장치 외부로 배출한다(개폐 밸브(4)는 열린 상태).

이상과 같이 본 발명의 실시 양태에 관하여 설명하였지만, 상술한 설명에 기초하여 당업자로서는 여러 가지 대체예, 수정 또는 변형이 가능하면서, 본 발명은 그 취지를 일탈하지 않는 범위에서 상술한 여러 가지 대체예, 수정 또는 변형을 포함하는 것이다.

1 진공 챔버
2 상부 전극
3 하부 전극
7 실리콘계 접착제
10 고주파 전원
PB 기판

Claims (3)

  1. 챔버 내에 한 쌍의 전극을 배치하고, 진공 상태가 된 챔버 내에 실리콘계 접착제를 개재하여 반도체 소자가 장착된 기판을 수납하여, 플라즈마 반응성 가스를 공급함과 동시에, 상기 한 쌍의 전극에 고주파 전원에 의해 고주파 전압을 인가하여 상기 반응성 가스를 플라즈마화하여 상기 기판을 세정하고, 이 세정한 후의 플라즈마화된 반응성 가스를 장치 밖으로 배출하는 플라즈마 세정 방법이며,
    처음에, 상기 반응성 가스로서 육불화황 가스를 사용하고, 육불화황 가스의 불소가 실리콘계 접착제에 포함되어 상기 반도체 소자의 표면에 부착된 실록산 중의 규소와 합체하여, 이 규소를 제거하고,
    이어서, 상기 반응성 가스로서 아르곤 가스를 사용하고, 이 아르곤 가스 중의 아르곤이 상기 반도체 소자 또는 이 반도체 소자가 장착된 기판에 부착된 황을 제거하고,
    상기 챔버의 탈기를 플라즈마 반응 가스를 공급하지 않고 규소 제거 후에 아르곤 가스의 사용 전에 하는 것을 특징으로 하는 플라즈마 세정 방법.

  2. 챔버 내에 한 쌍의 전극을 배치하고, 진공 상태가 된 챔버 내에 전극부가 은 도금으로 제작되고 실리콘계 접착제를 개재하여 반도체 소자가 장착된 기판을 수납하여, 플라즈마 반응성 가스를 공급함과 동시에, 상기 한 쌍의 전극에 고주파 전원에 의해 고주파 전압을 인가하여 상기 반응성 가스를 플라즈마화하여 상기 기판을 세정하고, 이 세정한 후의 플라즈마화된 반응성 가스를 장치 밖으로 배출하는 플라즈마 세정 방법이며,
    처음에, 상기 반응성 가스로서 육불화황 가스 및 산소 가스를 사용하고, 육불화황 가스의 불소가 실리콘계 접착제에 포함되어 상기 반도체 소자의 표면에 부착된 실록산 중의 규소와 합체하여 생성된 규소를 포함하는 합성 물질을 제거함과 동시에, 육불화황 가스의 황(S)이 산소 가스(O2)와 합체하여 생성된 황을 포함하는 합성 물질을 제거하고,
    이어서, 상기 반응성 가스로서 아르곤 가스를 사용하고, 이 아르곤 가스 중의 아르곤이 상기 반도체 소자 또는 이 반도체 소자가 장착된 기판에 부착된 황을 포함하는 합성 물질을 제거하고,
    상기 챔버의 탈기를 플라즈마 반응 가스를 공급하지 않고 규소 제거 후에 아르곤 가스의 사용 전에 하는 것을 특징으로 하는 플라즈마 세정 방법.

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