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박막 고체 산화물 연료전지를 위한 박막 공정

Thin Film Process for Thin Film Solid Oxide Fuel Cells - A Review

Journal of the Korean Society for Precision Engineering 2018;35(12):1119-1129.
Published online: December 1, 2018

1 서울대학� 기계항공공학부

2 캘리�니아대학� �너지연구센터

1 Department of Mechanical and Aerospace Engineering, Seoul National University ÿØÿàJFIFddÿìDuckydÿáqhttp://ns.adobe.com/xap/1.0/ ÿîAdobedÀÿÛ„ÿÀŠÿÄ     ! 1AQa"q� 2#w8ð‘¡ÁÑB3´µ6v¶7×X±Rr²$˜9áñb’C³Ãt%u&–ÖW·‚s'(xy¢ÂÓ4T”5f‡—ÇH¨¸Ø  !1AQaq"�‘¡2B ±ÁRbr#³´u67ðѲ3sTt5v8áñâSc$4Ä‚’¢C“ÔÔ%UÕÂÒÓ…•FVÅÿÚ ?ßàêÓ_A÷ú‹× ­j- ŠHÌûû>‚>Ì,šm*>½ôßÈÞfzp"áõö—£Téõ‹£—Ær÷Kkr¾ÒÙî��âœ^× »Òr.|_&€ã]¿|*œ™v¿P¶²uܶv”o‡±¿QÇ1Ÿ ¾�ŒŸmÍëw¾VJUöhu-ãIð"=L‹‡n§õ‘iù½AÆ•8Úö�"ûÛ²½þ„� ák�*Ò¿[yùu:ý.Ž‚v«U¤ÒÚQ+•)Ñá%F� D•Hy²V‡è×B훩kš>‘Hêy8øÓj©Ý¹ q~§9Dúñ4íKR‚þm±zõÚíQ„¥ßö)µ^Ê”Ó.J%k_tVi5NTê¥Ójg!'¡k©Çy|5as…¨ðÃOÏÁÈ»)R–¯Û¸ß©FMÔ¿3LÕ4çj¹6dÖùÚœ#êNIwUF©•]J ûq¡BŒô¹/(ËF™aãŠâfJöRzq3à\GÕ›™ ?ö~\£ 6å)6èý•Wµµ4¶m[O›ö^L0ìEË&r¤RMïØ¶*º×ÑC .ÍÂ]Un·l¥Š-1— 1ßr#Rj/¥´ø¯&QɈ׉˩·ás6­Rj=5Tgæ.´êy™.·PÓ¡:ÖJJíS«…÷:îßC8èÝ-Äù„2u]–d�&¢é»Òvøª·Uºz;¾»7p·9‘˜» 5Všã‰nLÖ¢µ£”¢"y)Ц">Ói×™Ñ(ûIDDd|œ¹Ö Yj0·­; L›§ãR¯fÙÞàÝS�˜:k¥ÚÃñtYäK%*ÒN2^ômñ|&dÄŸthó":‡ãÊe§Øy¾)u§P—¶ôQó¡ZöðW)gcC3Pv&“M¾ÇéM¯„ÂWìÏì¬d&¯Å´ãÛ²½�mvŸT¹èRoÞÕªM0Ü3ä*…F3Yº›dûèæãýÃ6¡®èÚ\8õ,¼\h÷Ý» kß”‘õâi¶¡<k× žÞNTõð¦wSëÔªº­Ñmljö•’j[>->±p£tU©Ôâ�%¯'§L‹R>&EÇBïôH$ßÝý�§ÉMQAU¶x[›$Z6’ÒÍv®Ôi&’_“a.K˜IQ{äh©yÆ’½ ’j"JùOCá ê×9òö—ìeäFŒªÒ�´ÞÿfŽjµîí;™ËšÎ©<[3”_m%ÃïÑ÷ ·•l‹¦Q@¥Ö4œ³Ñg²ü�=5$°™(J]YëÁ®c-OMqé<÷ÊÚõÇ�‡“ wSø²�¨¹z’œ«ïÚ—)kš$ÜË7ªV©I¥ïÅPý붾ͯnV+卵*t]i‚ÐŽD¥31ñí~S¨Añí1ûéÃCÐ2u)ÑÂʼnΛãQn-UÅoîi÷3ò´�:®«gß»rI8ý¯ÊØ“Wm*G zà«Ü•)ZÌ×§J}Åê§Yµ Y“lGeJ6ØcB2I ‹NS3×Qµ>kÔõÞ=KT›½ÅBëœâ—ÆÙÎT]ŠŽž‚W鿇¢ÂÞ6œ¬«Ü+ãSÓÛ¦ööï÷Ož—X©QgG©R¦? 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#E-mail: swcha@snu.ac.kr, TEL: +82-2-880-8050
• Received: September 22, 2018   • Revised: December 18, 2018   • Accepted: November 8, 2018

Copyright © The Korean Society for Precision Engineering

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고체 산화물 연료전지(Solid Oxide Fuel Cells, SOFCs)는 연료전지� 한 종류로서 �반�으로 �온전�성 세�믹(Ion Conduction Ceramic)� 전해질(Electrolyte)로 사용하는 연료전지�다. �온전�성 세�믹� 저온�서 전��(Conductivity)가 낮고, 온�가 높아질수� 전��가 향��기 때문� 고체 산화물 연료전지는 보통 700oC ��� 고온�서 작�한다. 고체 산화물 연료전지는 다른 �너지 변환장치나 혹� 다른 종류� 연료전지� 비해서 많� 장�� 가지고 있다. 고온�서 작�하기 때문� 물 관리 문제가 없으며, 저가� 촉매를 사용할 수 있고, 수소가 아닌 탄화수소 계열� 연료를 사용할 수 있다. �한 W 단위부터 MW 단위까지 용량� 쉽게 �용할 수 있고, 소�� 없고 경제성� 있는 장�� 있다. 하지만 높� 운전온�로 �해서 밀봉과 연결재(Interconnector)� 재료 선�� 있어 제한� 있으며, 시�과 정지� 많� 시간� 필요하고, 발전 시스템 구성� 위한 Balance of Plant (BOP) 구성� 많� 제한� 발�한다.1-4
높� 운전온�로 �한 문제�� 제거하기 위해서는 600 °C �하� 중온(Intermediate Temperature) 과 저온(Low Temperature)�서 고체 산화물 연료전지를 작�시켜야 한다. 낮� 온�로 �한 전해질과 전극� 저항� 최소화하기 위해 박막 �착 공정(Thin Film Deposition Process)� �용한 고체 산화물 연료전지가 박막 고체 산화물 연료전지(Thin Film Solid Oxide Fuel Cells, TF-SOFCs)�고 많� 연구가 수행�었다. TF-SOFCs는 고체 산화물 연료전지� 장�� �해서 많� 장�� 가지고 있다. TF-SOFCs는 운전온�가 �반�� 고체 산화물 연료전지보다 낮아서 시스템 작�� 빠르고, 박막 전해질� 사용하여 오믹 저항 �실� 최소화하였으며, 시스템� 소형으로 구성할 수 있다.5-8
박막 �착 공정� 통해서 제작�는 TF-SOFCs� 전극과 전해질� 요구�는 특성� 서로 다르다. 전해질� �온 전� 저항� 최소화하기 위해서 얇으면서� 연료 누설과 쇼트를 막기위해 결함� 없고 치밀한 구조가 필요하다. 전극� 연료 혹� 공기� 전달� �활하고 �성물� 쉽게 제거하고, 전기화학 반�� �어나는 전해질-촉매-기체가 만나는 삼�계면(Triple Phase Boundary) 최대화를 위한 다공성(Porous) 구조와 집전저항� 최소화할 수 있는 연결성(Connectivity)� 가져야 한다. 박막 �착 공정� 공정 방�� 따�서 장단�� 확실하다. 따�서 TF-SOFCs를 제작할 때는 �절한 박막 �착 공정� �용할 필요가 있다.
본 �설�서는 TF-SOFCs를 제작하기 위한 박막 공정� 특성과 연구 개발 �향� 요약 기술하고� 한다.
박막 �착 공정� 반�체, 디스플레�, 광학, 산업용 공구 등 여러 산업 분야�서 �리 �용�어 양산성, 신뢰성, 재현성� 검�한 공정�다. 박막 공정� �착 방�� 따�서 물리 기� �착과 화학 기� �착으로 분류할 수 있다. TF-SOFCs 연구�는 물리 기� �착과 화학 기� �착 모� �용�어 수행�었다.
2.1 물리 기� �착(Physical Vapor Deposition, PVD)
물리 기� �착� 고체 혹� 액체 소스�서 기화� ��들 혹� 분�들� 기체 �태� 형태로 화학반� 없� 기�� �착시키는 방법�다.9 �반�으로 물리 기� �착� 단� �소 박막, 합금 박막, 화합물 박막� �착할 수 있다. 물리 기� �착� 공정�서 소요�는 �너지를 절약할 수 있고, �기물� 최소화할 수 있다. 하지만, 화학 기� �착� 비해 단차피복성� 부족하며, 넓� 면�� 대한 균��가 낮다.
물리 기� �착� 종류로는 스�터�(Sputtering), 펄스 레�저 �착(Pulsed Laser Deposition, PLD), 전� 빔 �발장치(E-beam Evaporation), �온 빔 �움 �착(Ion Beam Assisted Deposition) 등� 있다. Fig. 1� � 물리 기� �착법� �리를 개략�으로 보여준다. 물리 기� �착� 기�과 타겟� 거리, 기�과 타겟 사�� �대� 위치, �착 압력, 기�� 온�, �착 공정 기체� 종류, 타겟� 가해지는 파워, 공정 기체� 유량 등� 공정 변수를 제어하여 요구�는 구조, 결정화 정�, �께를 갖는 박막� 제작할 수 있다.10 따�서 물리 기� �착� 반�체, 디스플레�, 태양광, 연료전지 등 다양한 산업분야� �리 활용�고 있다. �러한 여러 물리 기� �착 중� TF-SOFCs� 연구� �리 사용�는 것� 스�터�과 펄스 레�저 �착�다. 스�터�과 펄스 레�저 �착� TF-SOFCs� 전해질과 전극� �착하는� 모� 사용�어 왔다.
Fig. 1

Schematics of physical vapor deposition processes

KSPE_2018_v35n12_1119_f001.jpg
앞�서 언급했듯� TF-SOFCs� 전해질� 치밀하고 결함� 없는 구조를 가져야 한다. �시� 전해질� 통한 �온 전� 저항� 최소화하기 위해 가능한 얇� �께가 요구�다. 반면� 전극� 경우 삼�계면� 최대화하고, 반�물� 공급과 �성물� 제거를 위해 다공성 구조가 요구�다. 스�터�과 펄스 레�져 �착� �용하여 박막� �착할 때, �반�으로 공정 압력� 높아질수� 다공성 박막� �착�며, �착 온�가 높�수� 치밀하고 결정성� 좋� 박막� �착�다.5
스�터�� 고체�태� 타겟� 플�즈마를 통해 형성� �너지를 가진 �온들� 충�하여 표면� ��들� 분리시켜서 분리� ��들� 기�� �착�는 공정�다.11 스�터� 공정� 공정 변수 제어를 통해서 박막� 구조와 특성� 변화시키기 용�하여 TF-SOFCs 연구� 많� �용�었다. Stanford 대학� Prinz �수 연구실�서는 스�터�� �용하여 TF-SOFCs� �용하는 박막 전극과 전해질� 대한 연구를 많� 수행하였다.12-18 다공성 Pt 금� 연료극과 공기극� 스�터� 기법� �용하여 여러 종류� TF-SOFCs � 저온 고체 산화물 연료전지� �용하였다. 그 외 Pd, Ru, Ag 등 다양한 금�� 전극으로 �용하는 연구를 수행하였고, 특히 Pt 전극� 뭉침� 방지하여 성능열화를 막고 장기 안정성 강화를 위해 나노 어레� 전극� �� Pt 와 Ag 로 만들어 12시간� 걸친 장기안정성 개선효과를 확�하였다.14,16 �한 Pt 공기극� 개선� 위해 순수 Pt 전극� 아닌 Pt-Ni, Pt-Ag Alloy 연구� 수행�었다.17,19 �한 �트리아 안정화 지르코니아(Yttria Stabilized Zironia, YSZ), 가�리니아가 �핑� 세리아(Gadolinia Doped Ceria, GDC) 박막 전해질 � 기능층 �착� 관한 연구� 수행하였다. 스�터�� �용하여 50 nm - 150 nm �께� YSZ 전해질� Free Standing 형�� TF-SOFCs� �용하여 400oC�서 400 mW/cm2를 기�하였다.15
Harvard 대학�� Ramanathan �수 연구실�서� 스�터�� �용하여 YSZ 박막 전해질과 Pt, Pd, Ru� 연료극, 페로브스카�트 La1-xSrxCo1-yFeyO3-δ (LSCF), Ba0.5Sr0.5Co0.8Fe0.2O3 (BSCF) 공기극� Free Standing 타입 TF-SOFCs� �용하여 연구를 진행하였다.20-29 Free Standing 방�� TF-SOFCs� Pt 전극과 YSZ 전해질� �용하여 500oC�서 1037 mW/cm2를 기�하였다.30 �한 Pt가 아닌 다양한 귀금� 촉매를 연료극으로 �용하여 탄화수소연료�서 �가를 진행하였다. Pd 연료극과 YSZ 전해질� �용한 TF-SOFCs를 메탄 연료를 �용하여 특성� �가하였으며, 550oC�서 385 mW/cm2� 성능� 기�하였다.31 Ru� �용해서 500oC�서 450 mW/cm2� 성능� 보였고, Ru과 GDC 를 코-스�터�(Co-Sputtering)으로 연료극� �착하여 가습� 메탄� 연료로 485oC�서 275 mW/cm2를 기�하였다.23,24 특히 스�터�� �용하여 페로브스카�트 공기극 물질� LSCF와 BSCF를 �착하여 연구를 수행하였다. 70 nm �께� LSCF 공기극� �착하여 Free Standing 방�� TF-SOFCs� �용하여 �가하였다. Pt 연료극, YSZ 전해질, LSCF 공기극으로 �루어진 연료전지는 560oC�서 0.6 V� 개회로 전압과 120 mW/cm2� 성능� 보였다. �한 BSCF� 스�터�� �용하여 �착하고 TF-SOFCs� 공기극으로 �용하여 특성� �가하였다.32 BSCF 공기극� 가진 연료전지는 520oC�서 35 mW/cm2� 성능� 기�하였다.33
MIT Tuller �수 연구실�서� 스�터�� �용하여 YSZ 박막 전해질과 다공성 Pt 전극� �착하고 특성� 관한 연구를 진행하였다.34,35 YSZ 박막 전해질� Y2O3 ��� 따른 전� 특성� 관한 연구를 수행하였고, Pt를 반�성 스�터�(Reactive Sputtering) 기법� �용하여 �착 후 산소가 고온�서 분리�는 성징� �용하여 다공성 Pt 전극� 개발하였다.
Nanyang Technological University� Su �수 연구실�서� 스�터�� �용하여 Pt, Pd, Pt-Ni 합금 전극과 YSZ전해질� TF-SOFCs� �용하여 연구를 수행하였다.36-40 특히 Pt-Ni 합금 공기극� 경우 �반 Pt 전극� 비�하여 뭉침 현�� �한 성능 열화가 �어 장기 성능� 유리함� 보였다.40
고려대학� 심준형 �수 연구실�서는 다공성 Ni, Pt, Ag 전극, YSZ 전해질, 스칸디아 안정화 지르코니아(Scandia Stabilized Zirconia, ScSZ) 기능층 등� 스�터로 �착하여 연구를 수행하였다.41-46 특히 다공성 Ag 전극� �착하고 그 위� ScSZ 기능층� 얇게 �착해서 저온 고체 산화물 연료전지� �용하였� 때 �반 다공성 Pt 전극보다 450oC�서 10 mW/cm2 �� 우수한 성능� 보였다.44 기능층� YSZ 로 �용한 연구� 진행하였으며, 마찬가지로 Ag-YSZ 전극� 단순 Pt 전극보다 450oC�서 4배 정� 우수한 성능� 보였다.45
서울대학� 차�� �수 연구실�서� Pt 연료극 � 공기극, Ni 연료극, Ni-YSZ, Pt-GDC, Ni-GDC 등 �온 전� 혼합전�체(Mixed Ionic Electronic Conductor, MIEC) 전극과 YSZ, GDC, �트리아가 �핑� 세리아(YDC), 스칸디아 안정화 지르코니아(ScSZ), 등� 박막 전해질� 관한 연구� 수행하였다. 아노다�징 알루미늄 기�(Anodized Aluminum Oxide Template, AAO Template)를 �용한 TF-SOFCs�서 Pt 연료극� 기공�와 �께가 TF-SOFCs� 성능� 미치는 �향� 연구하였고 연료극� �께가 ��고 기공�가 높�수� 높� 성능� 측정하였다.47 코-스�터� 기법� �용하여 Ni-YSZ, Ni-GDC, Pt-GDC 등� MIEC 전극 공정� 개발하고 �� TF-SOFCs� 연료극과 공기극으로 �용하여 연구를 수행하였다.48-52 코-스�터� 기법으로 �착한 Pt-GDC 공기극� 가진 저온 고체 산화물 연료전지가 �반 다공성 Pt 전극보다 높� 성능� 보�고, 장기성능�� 유리한 것� 확�하였다. �한 서울대학��서는 ScSZ를 TF-SOFCs� 전해질로 �용하고 GDC와 �중층 박막 전해질로 형성할 때 최�화 연구를 진행하였다.53,54 GDC를 공기극 기능층으로 활용하여 저온 고체 산화물 연료전지�서 최� �께를 구하는 연구� 수행하였고, �한 GDC를 연료극 기능층으로서 활용하여 �핑� 세리아 기능층� 성능� 미치는 �향� 연구하였다.55,56 500oC�서 20 nm� GDC 연료극 기능층� 들어간 TF-SOFCs는 YSZ 전해질로만 �루어진 연료전지보다 ~30% 정� 성능 향�� 보였다.
서울과학기술대학� 안지환 �수 연구실�서� 마찬가지로 Pt 전극과 사마리아 �핑� 세리아(SDC), GDC 등� 기능층으로 활용하는 연구를 수행하였다.57,58 특히 SDC 와 ��막 �착(Atomic Layer Deposition, ALD) YSZ를 혼합한 샌드위치 전해질� �용한 TF-SOFCs를 �용하여 450oC�서 562 mW/cm2� 성능� 측정하였다.59
한양대학� 김�범 �수 연구실� 스�터�� �용하여 Pt와 Ni 등 다공성 금� 박막 전극과 안정화 지르코니아 계열 � �핑� 세리아 계열� 박막 전해질� TF-SOFCs와 저온 고체 산화물 연료전지� �용한 연구를 수행하였다.60-66 특히 한양대학��서는 스�터��서 ScSZ타겟� �가� 파워를 변화시켜 표면 Grain� �기를 줄여서 공기극 기능층으로 �용한 연구를 수행하였고, 450oC�서 479 mW/cm2를 기�하였다.64
스�터�� �용한 박막 전극� 경우 대부분 다공성� Pt 전극� 공기극으로 �용하고 있으며, 연료극� 경우 연료 � 목�� 따�서 다양한 기공�와 �께를 갖는 Pt, Pd, Ru, Ni 전극� 연구�었다. 전해질� 치밀한 구조를 갖는 YSZ, ScSZ, GDC, YDC, SDC등� 전해질� 대한 연구가 수행�었다. 스�터�� �용한 전해질 연구는 산소 �온 전�체� 집중�어 있다. 기존� 세�믹 타겟과 합금 타겟� �용한 반�성 스�터�� 통해서 �하는 전해질� �착하는 연구가 많� 수행�었다.
Table 1� 스�터�� �용한 박막 전극 � 전해질� 관한 연구를 요약하였다. 전극 관련해서는 스�터� 기법� �용하여 단순 전극�나 전해질 �착� 아닌, 코-스�터� 기법� 활용한 MIEC 전극과 공기극 전극� 대한 얇� 기능층 관련 연구가 많� 진행�었다. 특히 다공성 금� 전극� 경우 공기극� 관한 연구가 집중�으로 수행�고 있다. 스�터�� �용하여 나노 다공성 구조로 제작한 Pt 전극� 온�� 따�서 뭉침 현�� 발�하여 성능열화가 �기는 한계를 가지고 있다. �를 방지하고 장기 안정성과 성능� 향�시키기 위하여 합금 공기극, 코-스�터� 기법� �용한 공기극, 전극 표면� 전해질 물질로 가�게 �핑하는 방법� 연구�고 있다. �한 고가� Pt 전극 촉매를 대체하기 위해 연료극� Ni과 Ni� 사용하는 MIEC 전극� 대한 연구가 수행�고 있으며, 공기극으로는 Ag를 �용한 연구가 수행�었다.
Table 1

Materials prepared by sputter process

Table 1
전극 전해질/기능층 Reference
Stanford Pt, Pd,
Ru, Ag,
Pt-Ni,
Pt-Ag,
YSZ, GDC 12-19
Harvard Pt, Pd,
Ru-GDC,
LSCF
BSCF
YSZ, GDC 20-33
MIT Pt, Pt-O YSZ 34, 35
NTU Pt, Pd,
Pt-Ni
YSZ 36-40
고려대학� Pt, Ag,
Ag-YSZ,
Ag-ScSZ
YSZ, ScSZ 41-46
서울대학� Pt, Ni,
Pt-GDC,
Ni-YSZ,
Ni-GDC
YSZ, GDC
ScSZ, YDC
BYZ
47-56
서울과학기술대학� Pt SDC 57-59
한양대학� Pt YSZ, ScSZ
GDC, SDC
60-66
펄스 레�저 �착� 고�너지� �외선 레�저 펄스를 고체 타겟� 조사시키면 타겟 표면� ��들 �러스터들� �발�면서 입�들로 형성� Plume� 형성하게 �고, � Plume� �용하여 기�� 물질� �착하는 방법�다.11,67 펄스 레�저 �착� �대�으로 시스템 설계 � 설치가 용�하고, 파우�, 소결� 타겟, 단결정 타겟등 다양한 형태� 물질� �용하여 �착할 수 있지만, �착 면�� 제한���는 단�� 있다.
Stanford 대학�� Prinz �수 연구실� 펄스 레�저 �착� �용하여 130 nm �께� 프로톤(Proton) 전�체� �트리아가 �핑� 바륨 지르코네�트(Y-doped Barium Zirconate, BYZ) BYZ 전해질� Free Standing 형� TF-SOFCs� �용하였다. BYZ 전해질� 갖는 Free Standing TF-SOFCs는 400 °C �서 120 mW/cm2� 성능� 보였다.68 �한 BYZ� 결정형태가 전��� 미치는 �향� 대해서� 연구하였다. 다결정(Polycrystalline)� BYZ는 Grain 경계가 �온전�를 방해하여 Epitaxial 하게 성장한 단결정(Single Crystal)으로 �착한 BYZ 보다 전��가 낮았다.69 YSZ, GDC와 YDC를 공기극 기능층으로 활용하는 연구를 진행하였다.70-74 �핑� 세리아는 안정화 지르코니아 보다 표면 �환 계수와 산소 확산�가 높아서 공기극�서 발�하는 분극 저항 �실� 줄� 수 있었으며, GDC를 공기극 기능층으로 �용한 저온 고체 산화물 연료전지는 �반 YSZ 전해질만� �용한 고체 산화물 연료전지� 비해서 2배 높� 성능� 보였다.70 펄스 레�저 �착 후 어��� 통해 표면 Grain� �기를 변화시켜 Grain� �기와 Grain 경계 밀�가 저온 고체 산화물 연료전지� 성능� 미치는 �향� 연구하였고, 표면 Grain� �기가 작아서 Grain 경계 밀�가 높�수� 산소 공�(Vacancy) 밀�가 높아 연료전지� 성능� �가함� 보였다.73
Kyushu 대학� Ishihara �수 연구실�서� 펄스 레�저 �착� �용하여 La0.9Sr0.1Ga0.8Mg0.2O3-δ (LSGM) 전해질과 Sm0.5Sr0.5CoO3 (SSC) 공기극� �착하는 연구를 수행하였다. LSGM 과 SDC �중층 전해질과 SSC 공기극� �용한 연료전지는 500oC�서 500 mW/cm2� 성능� 보였다.75
Nanyang Technological University� Su �수 연구실�서� 펄스 레�저 �착� �용하여 BYZ, GDC, BSCF를 �� 박막 전해질과 전극으로 �용하는 연구를 수행하였다. 특히 프로톤 전� 물질� BYZ 를 전해질로, 산소 �온 전� 물질� GDC 를 공기극 기능층으로 �용한 TF-SOFCs가 425oC�서 445 mW/cm2� 성능� 보였다.76
서울대학� 차�� �수 연구실� 펄스 레�저 �착� �용하여 프로톤 전�성 물질� BYZ 전해질과 페로브스카�트 공기극 물질� LSCF� 대한 연구를 진행하였다.77-80 펄스 레�저 �착� �용한 BYZ 전해질� 높� 압력�서 �착하면 �께가 �가할수� 표면 거칠기가 �가했고, 박막 BYZ 전해질� �용한 TF-SOFCs는 450oC�서 44 mW/cm2� 성능� 보였다.79
한국 과학 기술연구�(KIST)� 고온 �너지 연구센터와 고려대학� 심준형 �수 연구실� 공�으로 펄스 레�저 �착� �용하여 YSZ, BZY, BYC, Y-doped Ba(Ce,Zr)O3 (BCZY) 전해질과 Ni-BZY, MIEC 연료극 기능층 �착� 관한 연구를 진행하였다.81-83 KIST와 고려대학��서 펄스 레�저 �착� �용해 BZY 전해질과 Ni-BZY 연료극 기능측� �용한 연료전지는 600oC�서 740 mW/cm2� 성능� 보였다.82 �한 비슷하게 Ni-BCZY 연료극 기능층과 BCZY 전해질� 펄스 레�저 �착으로 �용한 연료전지는 600oC�서 1.1 W/cm2� 성능� 보였다.83 �한 KIST는 펄스 레�저 �착� �용하여 Ni-YSZ 연료극 기능층, YSZ 전해질, GDC 공기극 기능층, LSC MIEC 공기극 전극물질� 연료극지지체형 연료전지� �용하여 많� 연구를 수행하였다.84-91
Table 2� 펄스 레�져 �착� �용한 TF-SOFCs 연구를 요약하였다. 펄스 레�저 �착� �용한 박막 �착� 대면�화가 어려워 양산성� 부족하다는 단�� 있지만, �반�� 물리 기� �착� 어려운 페로브스카�트 전극 물질� �함한 대부분� 세�믹과 금� 물질� �착할 수 있어서 TF-SOFCs, 저온 고체 산화물 연료전지� 연구� 많� �용�었다.
Table 2

Materials deposited by PLD process

Table 2
전극 전해질/기능층 Reference
Stanford YDC, GDC,
BYZ
68-74
Kyushu SSC LSGM 75
NTU BSCF BYZ, GDC 76
고려대학� LSC Ni-BZY,
Ni-BCZY,
BZY, GDC
81-83
서울대학� LSCF BYZ 77-80
한국과학기술연구� LSC,
LSM
Ni-YSZ, BZY,
BCZY, GDC
84-91
스�터�과 펄스 레�저 �착� �착 압력, 기� 온�, 가스 조성 등� 변화시켜서 �유롭게 �하는 조성과 구조를 가진 박막� 형성할 수 있다. 따�서 Table 1과 Table 2� 나온 것처럼 스�터�과 펄스 레�저 �착� �용하여 TF-SOFCs� 연료극, 공기극, 전해질, 기능층� 관한 연구 모� 활발하게 수행�고 있�� 알 수 있다.
2.2 화학 기� �착 (Chemical Vapor Deposition, CVD)
화학 기� �착� 열�나 플�즈마� �너지를 �용하여 기체 �태�서� 화학반�� 통해서 박막� �착하는 방��다. 화학반�� �용한다는 ��서 물리� 기� �착법과 �리가 다르다. 화학반�� �으키기 위한 �너지로는 가열� 기�으로부터� 열�너지 혹� 플�즈마를 �용한다. 화학 기� �착� �반�으로 물리 기� �착보다 복잡한 형�� 3차� 구조를 모� �착할 수 있고, 박막� 조성� 있어 유연성(Flexibility)를 가지고 있다. 하지만 화학 기� �착� �반�으로 높� 온�(> 600oC)가 요구�며, 유해한 전구체(Precursor)를 �용해야 하고, 유�성 부산물� �성�어 처리 문제가 있다.92 대표�� 화학 기� �착법으로는 플�즈마 강화 화학 기� �착(Plasma Enhance Atomic Layer Deposition, PECVD), 플�즈마 강화 ��막 �착(Plasma Enhance Atomic Layer Deposition, PEALD), ��막 �착(ALD)� 있다. 화학 기� �착� �반�으로 단차피복성(Step Coverage)� �대�으로 우수하며, 고품질� 우수한 박막� �착할 수 있어 반�체 공정� 많� 사용�다.93-98 특히 ��막 �착� 경우 �반�� 화학 기� �착/플�즈마 강화 화학 기� �착보다 낮� 온��서 옴스트롱(Å) 단위� �께 조절� 가능하고, 전구체나 반�물� 유�� �대�으로 � 민�하며, 복잡한 구조� 기��� 거� 100%� 해당하는 단차피복성� 보�며, 전체 기��서� 균��가 매우 높� 특성� 가지고 있다.
�한 플�즈마 강화 ��막 �착� 경우 ��막 �착� 특성� �해서 플�즈마� �용으로 �한 고품질, 낮� 결함� 박막� �착할 수 있고, ��막 �착 공정 온�� 범위를 늘릴 수 있고, 박막� 결정성� 개선할 수 있다. Fig. 2는 플�즈마 화학 기� �착과 ��막 �착� �리를 개략�으로 표시하였다. 화학 기� �착법 중� TF-SOFCs� 연구� �리 사용�는 방법� ALD�다. Stanford� Prinz �수 연구실�서는 ��막 �착� �용하여 YSZ, BYZ, YDC를 �� TF-SOFCs� 전해질과 공기극 기능층으로 �용하여 연구를 수행하였다. ALD로 �착한 110 nm �께� BYZ 전해질� �용한 Free Standing 형� TF-SOFCs는 400oC�서 136 mW/cm2� 성능� 보여 펄스 레�저 �착� �용한 TF-SOFCs보다 우수한 성능� 보였다.68
Fig. 2

Schematics of chemical vapor deposition processes

KSPE_2018_v35n12_1119_f002.jpg
�한 ALD를 �용하여 Y2O3� ��를 달리하여 1 nm� YSZ 공기극 기능층� �착하고 �향� 연구하였다. 1 nm� 공기극 기능층� Y2O3� 최� ��가 14 - 19 mol%� 때 Y2O3� �해 산소 공�� 많� 발�하여 성능� 50% �가함� 확�하였다.99,100 �한 ��막 �착� �용하여 Pt� �착하여 공기극� 성능� 향�시키거나 박막� 성장 정�를 �용해서 ��막 �착으로 형성� Pt 박막� 공기극으로 �접 �용하는 연구� 진행하였다.101,102 �한 Pt� YSZ와 혼합해서 �착하여 공기극 기능층으로서 TF-SOFCs� 성능� 향�시키는 연구� 수행하였다.103
Nanyang Technological University� Su �수 연구실�서� ALD를 �용하여 Pt 공기극� 얇� ZrO2 단� 막으로 �핑(capping)하여 장기성능� 확�하였다. 최� 싸��� ZrO2 박막으로 �핑� Pt 공기극� 분극저항� 1/6로 �소하고 성능� 향��었으며, ZrO2로 �핑�Pt 공기극� �반 Pt 공기극보다 450oC�서 120시간 장기 �가 결과 뭉침� �한 성능 열화가 50% �� 개선�어 �반 Pt 전극 보다 장기 안정성� 우수했다.104
고려대학� 심준형 �수 연구실�서� ��막 �착� �용하여 전해질로서는 YSZ와 촉매로서 Ru� �착하여 TF-SOFCs� �용하여 연구를 수행하였다.42,43,105–108
ALD를 �용해 Ru 촉매를 Pt 전극위� 싸��� 달리해서 �착하고 �탄올 연료를 �용해서 400oC - 500oC �역�서 연구를 수행했다. Ru 촉매를 �착한 연료전지가 �반 Pt 전극보다 높� 성능� 보�고, 장기 성능� 우수했다.42 �한 Ni 연료극 전극� Ru� ALD로 �착해서 메탄올로� �가를 진행하였으며, 마찬가지로 �반 Ni 보다 우수한 성능과 장기안정성� 보였다.43
서울대학� 차�� �수 연구실�서� ALD와 PEALD를 �용하여 YSZ를 �착하여 연구를 수행했다.109-111 ALD를 �용하여 YSZ를 박막 전해질로 �용한 연구� �해서, 얇� YSZ를 다공성 Pt 공기극 전극위� 기능층으로 �착하여 TF-SOFCs� �용하였� 때 성능� 향��고, Pt� 뭉침 현�으로 �한 성능 열화를 완화시켜 장기성능� 우수하게 유지�는 것� 확�하였다.112 �한 Pt 박막� ALD로 TF-SOFCs� 전해질과 공기극 사�� 계면� �착하여 기능층으로서 성능� �가하는 연구� 수행하였다. Pt 기능층� �용한 TF-SOFCs는 450oC�서 110 mW/cm2� 성능� 보였다.113 �한 PEALD를 �용하여 박막 YSZ를 전해질로 하는 TF-SOFCs를 제작하고 �가하였다. PEALD YSZ는 전해질 �께가 �가함� 따�서 표면� grain� �기가 �가하여 공기극 분극저항� �가하고 성능� �소하였다.114 �한 PEALD YSZ를 보호층으로 하는 �중층 박막 전해질� �용한 TF-SOFCs� 대해 �가하여 450oC�서 182 mW/cm2� 성능� 기�하였다.
ALD를 �용한 YSZ 연구�서는 서울과학기술 대학� 안지환 �수 연구실�서는 SDC� 환�� �한 전� 전�성 발현� 막기 위한 기능층으로서 매우 얇� �께(~25 nm)를 샌드위치 구조� 전해질� �용하여 연구를 수행하였다. 3중 샌드위치 구조 전해질� 갖는 TF-SOFCs는 450oC�서 562 mW/cm2� 성능� 보였다.59
Table 3�는 ALD를 �용한 TF-SOFCs연구를 요약하였다. ALD를 �용한 연구는 결함없는 치밀한 막� �착할 수 있다는 특성� �용하여 주로 전해질� 치중�어 수행�었다. 특히 산소 �온전�성 YSZ 관련 연구와 프로톤 전�성 BYZ 관련 연구가 진행�었으며, 근래� CeO2를 사용하는 전해질 � 기능층� 관한 연구가 수행�었다. �한 전해질 물질� 물리 기� �착으로 제작한 박막 전극� �용하여 장기 안전성과 성능� 향�시키는 연구� 수행�었다. �한 ALD� 우수한 단차피복성� �용하여 침투법(Infiltration)� �용하여 Pt, Ru 와 같� 촉매 물질� �용한 고성능 전극� 관한 연구가 수행�었다.
Table 3

Materials deposited by atomic layer deposition (including plasma enhanced atomic layer deposition)

Table 3
전극 전해질/기능층 Reference
Stanford Pt YSZ, BYZ,
YDC
18, 68,
94
99-103
NTU ZrO2 104
고려대학� Pt, Ru YSZ, CeO2 41-43,
105-108
서울대학� Pt YSZ
(Thermal, PEALD)
109-114
서울과학기술대학� YSZ 59
고체 산화물 연료전지� 전해질 혹� 전극� 박막공정� �용하거나, 전체를 박막 공정으로 제작한 TF-SOFCs는 전해질� �께를 최소화하고 기능층 � 촉매활성�가 높� 촉매를 사용하여 낮� 온��서(< 600oC)�서 높� 성능� 보였다.
박막 �착 공정� �착 특성� 따�서 물리 기� �착과 화학 기� �착 공정으로 나눌 수 있다. 여러 물리 기� �착 중� TF-SOFCs�는 주로 스�터�과 펄스 레�저 �착� 사용�다. 물리 기� �착� 공정 변수 조절� 통해서 �대�으로 쉽게 박막� 구조, 성분 등� 변경할 수 있으며, TF-SOFCs� 연료극, 공기극, 전극기능층, 전해질 �착� 모� �용�어 연구�었다. 스�터�과 펄스 레�저 �착� �함한 물리 기� �착� 새로운 전극과 전해질 물질� �착 공정 개발, 기존 전극과 전해질 한계 극복� 위한 공정 변수 확보 등� 필요하다.
화학 기� �착� 물리 기� �착보다 복잡한 3차� 구조� 잘 �착�고 결함� 없는 치밀한 막� 구성할 수 있어 주로 TF-SOFCs� 전해질� �착하는� 사용�다. 특히 화학 기� �착중� ALD와 PEALD는 우수한 단차피복성과 결함� 없고 치밀한 막� �착할 수 있는 특성� �용하여 TF-SOFCs� 전해질 �착� 많� �용�었으며, 전극, 전극 기능층으로� 연구가 수행�었다. 화학 기� �착� 기존 전해질 물질� 기능성 강화, 신규 전극과 전해질 물질 �착 공정 개발, 구조 변화를 위한 공정 개발� 필요하다.
물리 기� �착� 공정 변수 제어를 통해 쉽게 �하는 구조를 가진 박막 전극, 전해질, 기능층� 형성할 수 있는 장�� 있지만, 결함� 없는 치밀한 전해질� 형성하기 위해서는 �대�으로 �꺼운 �께가 필요하고, 다공성 금� 전극� 고온�서 뭉침현�으로 성능 열화가 발�하는 단�� 있다. ��막 �착� 단차피복성� 우수하고, �께를 정밀하게 제어 가능하며, 결함� 없는 박막� 형성할 수 있는 장�� 있지만, 막� 구조를 �유롭게 변경하기 힘들다는 단�� 있다. 따�서 TF-SOFCs를 제작하기 위해서는 전극, 전해질, 기능층� �합한 박막 공정� �용해야 한다. �한, 물리 기� �착과 화학 기� �착� ��� 장�� �절히 융합한 새로운 전극, 전해질, 기능층� 관한 연구가 필요하다.
본 연구는 2018년� 미래창조과학부� 재�으로 글로벌 프론티어 R&D 프로그램� 지�과(2012M3A6A7054855), 2015년� 산업통���부� 재�으로 한국 �너지 기술�가�(KETEP)� 지�과(No. 20153030040930)(KIST 2E26590), 과학기술정보통신부� 재�으로 한국연구재단(NRF)� 통한 미래 소재 디스커버리사업� 지�(2017K2A9A2A08000197)� 받아 수행한 연구 과제입니다.
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Gu Young Cho
KSPE_2018_v35n12_1119_bf001.jpg
Postdoctoral Researcher in the Center for Energy Research, University of California San Diego. His research interest is thin film solid oxide fuel cells (TF-SOFCs) and plasma enhanced atomic layer deposition.
Yoon Ho Lee
KSPE_2018_v35n12_1119_bf002.jpg
Postdoctoral Researcher in the Center for Energy Research, University of California San Diego. His research interest is thin film solid oxide fuel cells (TF-SOFCs).
Suk Won Cha
KSPE_2018_v35n12_1119_bf003.jpg
Professor in the Department of Mechanical Engineering, Seoul National University. His research interest is fuel cells, thin films and renewable energy system.

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Thin Film Process for Thin Film Solid Oxide Fuel Cells - A Review
J. Korean Soc. Precis. Eng.. 2018;35(12):1119-1129.   Published online December 1, 2018
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Thin Film Process for Thin Film Solid Oxide Fuel Cells - A Review
J. Korean Soc. Precis. Eng.. 2018;35(12):1119-1129.   Published online December 1, 2018
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Thin Film Process for Thin Film Solid Oxide Fuel Cells - A Review
Image Image
Fig. 1 Schematics of physical vapor deposition processes
Fig. 2 Schematics of chemical vapor deposition processes
Thin Film Process for Thin Film Solid Oxide Fuel Cells - A Review
전극 전해질/기능층 Reference
Stanford Pt, Pd,
Ru, Ag,
Pt-Ni,
Pt-Ag,
YSZ, GDC 12-19
Harvard Pt, Pd,
Ru-GDC,
LSCF
BSCF
YSZ, GDC 20-33
MIT Pt, Pt-O YSZ 34, 35
NTU Pt, Pd,
Pt-Ni
YSZ 36-40
고려대학� Pt, Ag,
Ag-YSZ,
Ag-ScSZ
YSZ, ScSZ 41-46
서울대학� Pt, Ni,
Pt-GDC,
Ni-YSZ,
Ni-GDC
YSZ, GDC
ScSZ, YDC
BYZ
47-56
서울과학기술대학� Pt SDC 57-59
한양대학� Pt YSZ, ScSZ
GDC, SDC
60-66
전극 전해질/기능층 Reference
Stanford YDC, GDC,
BYZ
68-74
Kyushu SSC LSGM 75
NTU BSCF BYZ, GDC 76
고려대학� LSC Ni-BZY,
Ni-BCZY,
BZY, GDC
81-83
서울대학� LSCF BYZ 77-80
한국과학기술연구� LSC,
LSM
Ni-YSZ, BZY,
BCZY, GDC
84-91
전극 전해질/기능층 Reference
Stanford Pt YSZ, BYZ,
YDC
18, 68,
94
99-103
NTU ZrO2 104
고려대학� Pt, Ru YSZ, CeO2 41-43,
105-108
서울대학� Pt YSZ
(Thermal, PEALD)
109-114
서울과학기술대학� YSZ 59
Table 1 Materials prepared by sputter process
Table 2 Materials deposited by PLD process
Table 3 Materials deposited by atomic layer deposition (including plasma enhanced atomic layer deposition)