• 제목/요약/키워드: Pt-Ru/C

검색결과 81건 처리시간 0.022초

Ru/RuO$_2$ 이중 전극위에 성장한 PZT 박막의 특성에 관한 연구 (The study of the properties of PZT thin films deposited on Ru/RuO$_2$ electrode)

  • 최장현;강현일;박영;송준태
    • 한국전기전자재료학회:학술대회논문집
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    • 한국전기전자재료학회 2001년도 추계학술대회 논문집
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    • pp.394-397
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    • 2001
  • In this paper, in-situ deposited Ru/RuO$_2$ bottom electrodes have been investigated as new bottom electrodes for PZT thin film capacitor application. As a comparison, structural and electrical properties of PZT thin films on Pt/Ti and RuO$_2$ bottom electrodes are also investigated. The use of Ru/RuO$_2$ hybrid electrodes showed better electrical properties in compression with RuO$_2$ bottom electrode. With increasing Ru electrode thickness, the PZT thin films showed preferred orientation along the (110) direction and leakage current of PZT thin films were improved. The PZT thin films on Ru (100nm)/RuO$_2$ electrodes exhibited excellent ferroelectric properties such as remant polarization and coercive field of 7.2 C/$\textrm{cm}^2$ and 46.35 kV/cm, respectively.

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Nanophase Catalyst Layer for Direct Methanol Fuel Cells

  • Chang Hyuk;Kim Jirae
    • 전기화학회지
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    • 제4권4호
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    • pp.172-175
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    • 2001
  • 마그네트론 스퍼터링 방법에 의하여 Nanophase 촉매층을 형성하여 Direct Methanol Fuel Cell(DMFC)에 적용하였다. 일반적인 박막 증착 방법보다 높은 압력 (Ar/He혼합기체)에서 금속 Target과 탄소 Target을 동시에 스퍼터링하여 내피온막 위에 직접 코팅함으로써 기공성 있는 PtRu혹은 Pt및 탄소입자를 포함한 새로운 구조의 촉매층을 형성하였다. 본 방법에 의하여 $1.5mg/cm^2$의 PtRu(Anode) 및 $1mg/cm^2$ Pt(Cathode) 로딩으로 2M Methanol, 1 Bar공기, $80^{\circ}C$조건에서 $45mW/cm^2$의 출력을 얻을 수 있었으며, 이는 기존의 상용방법에 의하여 제조된 전극보다 같은 조건에서 $30\%$의 성능향상을 제시한 것이다. 이는 Nanophase촉매층 구조로 인하여 초미세 분말을 적용하였고, 많은 량의 원자들이 입계에 배열하게 됨으로써 촉매반응을 원활하게 하고,연료의 공급을 효율적으로 해준 것에 기안한 것으로 판단된다. 그러므로, 본 연구의 결과를 응용할 경우 DMFC를 휴대용 전자기기에 적용함에 있어서 성능향상 및 가격경쟁력 확보에 도움을 줄 것으로 기대된다.

산화제 생성율이 높은 촉매성 산화물 전극(DSA)의 개발에 관한 연구(II) (A Study on the Preparation of the Dimensionally Stable Anode(DSA) with High Generation Rate of Oxidants(II))

  • 박영식;김동석
    • 한국환경과학회지
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    • 제18권1호
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    • pp.61-72
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    • 2009
  • Fabrication and oxidants production of 3 or 4 components metal oxide electrode, which is known to be so effective to destruct non-biodegradable organics in wastewater, were studied. Five electrode materials (Ru as main component and Pt, Sn, Sb and Gd as minor components) were used for the 3 or 4 components electrode. The metal oxide electrode was prepared by coating the electrode material on the surface of the titanium mesh and then thermal oxidation at $500^{\circ}C$ for 1h. The removed RhB per 2 min and unit W of 3 components electrode was in the order: Ru:Sn:Sb=9:1:1 > Ru:Pt:Gd=5:5:1 > Ru:Sn=9:1 > Ru:Sn:Gd=9:1:1 > Ru:Sb:Gd=9:1:1. Although RhB decolorization of Ru:Sn:Sb:Gd electrode was the highest among the 4 components electrode, the RhB decolorization and oxidants formation of the Ru:Sn:Sb=9:1:1 electrode was higher than that of the 3 and 4 components electrode. Electrogenerated oxidants (free Cl and $ClO_2$) of chlorine type in 3 and 4 components electrode were higher than other oxidants such as $H_2O_2\;and\;O_3$. It was assumed that electrode with high RhB decolorization showed high oxidant generation and COD removal efficiency. OH radical which is electrogenerated by the direct electrolysis was not generated the entire 3 and 4 components electrode, therefore main mechanism of RhB degradation by metal oxide electrode based Ru was considered indirect electrolysis using electrogenerated oxidants.

1,2-Dichlorobenzene 및 질소산화물 동시제거를 위한 촉매연구 (A Study on Catalysts for Simultaneous Removal of 1,2-Dichlorobenzene and NOx)

  • 박광희;홍성창
    • 공업화학
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    • 제20권5호
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    • pp.522-526
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    • 2009
  • 다양한 금속(Ru, Mn, Co, Fe)을 $Al_2O_3$$CeO_2$에 담지한 촉매를 이용하여 1,2-Dichlorobenzen (1,2-DCB) 제거를 위한 촉매산화 실험을 실시하였다. 이와 더불어 동시에 NOx 제거가 이루어져 단일 촉매층에서 산화/환원 이원 기능이 가능한 촉매를 연구하고자 하였다. 실험결과 1,2-DCB 산화제거효율은 Ru/Co/$Al_2O_3$, Mn-Fe/$CeO_{2}$, 상용촉매인 Cr/$Al_2O_3$ 순으로 나타났다. 또한 1,2-DCB 산화제거효율이 가장 우수하였던 Ru/Co/$Al_2O_3$는 Chlorobenzene (CB)의 분해실험에서도 VOC 제거에 있어서 잘 알려진 Pt-Pd/$Al_2O_3$ 보다 우수한 활성을 나타내었다. 또한 $Cl_2$와 같은 생성물에 의하여 활성의 저하 및 황에 대한 내피독성과 내구성에서 우수한 결과를 얻을 수 있었다. NOx 제거에 있어서도 $260^{\circ}C$에서 NOx 전환율이 70% 정도로 나타났다.

Assessment of direct glycerol alkaline fuel cell based on Au/C catalyst and microporous membrane

  • Yongprapat, Sarayut;Therdthianwong, Apichai;Therdthianwong, Supaporn
    • Advances in Energy Research
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    • 제2권1호
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    • pp.21-31
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    • 2014
  • The use of a microporous membrane along with Au/C catalyst for direct glycerol alkaline fuel cell was investigated. In comparison with Nafion 112, the microporous Celgard 3401 membrane provides a better cell performance due to the lower ionic resistance as confirmed by impedance spectra. The single cell using Au/C as anode catalyst prepared by using PVA protection techniques provided a higher maximum power density than the single cell with commercial PtRu/C at $18.65mW\;cm^{-2}$ The short-term current decay studies show a better stability of Au/C single cell. The higher activity of Au/C over PtRu/C was owing to the lower activation loss of Awe. The magnitude of current decay indicates a low problem of glycerol crossover from anode to cathode side. The similar performance of single cell with and without humudification at cathode points out an adequate transport of water through the microporous membrane.

Enhancement of Photocurrent Generation by C60-encapsulated Single-walled Carbon Nanotubes in Ru-sensitized Photoelectrochemical Cell

  • Lee, Jung-Woo;Park, Tae-Hee;Lee, Jong-Taek;Jang, Mi-Ra;Lee, Seung-Jin;Kim, Hee-Su;Han, Sung-Hwan;Yi, Whi-Kun
    • Bulletin of the Korean Chemical Society
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    • 제33권8호
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    • pp.2689-2693
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    • 2012
  • Single-walled carbon nanotubes (SWNTs) and $C_{60}$-encapsulated SWNTs ($C_{60}@SWNTs$) are introduced to Ru-sensitized photoelectrochemical cells (PECs), and photocurrents are compared between two cells, i.e., an $RuL_2(NCS)_2$/DAPV/SWNTs/ITO cell and an $RuL_2(NCS)_2$/DAPV/$C_{60}@SWNTs$/ITO cell. [L = 2,2'-bipyridine-4,4'-dicarboxylic acid, DAPV = di-(3-aminopropyl)-viologen, and ITO = indium-tin oxide] The photocurrents are increased by 70.6% in the presence of $C_{60}@SWNTs$. To explain the photocurrent increase, the reverse-field emission method is used, i.e., $RuL_2(NCS)_2$/DAPV/SWNTs/ITO cell (or $RuL_2(NCS)_2$/DAPV/$C_{60}@SWNTs$/ITO cell) as an anode and a counter electrode Pt as a cathode in the external electric field. The improved field emission properties, i.e., ${\beta}$ (field enhancement factor) and emission currents in the reverse-field emission with $C_{60}@SWNTs$ indicate the enhancement of the PEC electric field, which implies the improvement of the electron transfer rate along with the reduced charge recombination in the cell.

The Operation of Polymer Electrolyte Membrane Fuel Cell using Hydrogen Produced from the Combined Methanol Reforming Process

  • Park, Sang Sun;Jeon, Yukwon;Park, Jong-Man;Kim, Hyeseon;Choi, Sung Won;Kim, Hasuck;Shul, Yong-Gun
    • Journal of Electrochemical Science and Technology
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    • 제7권2호
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    • pp.146-152
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    • 2016
  • A combined system with PEMFC and reformer is introduced and optimized for the real use of this kind of system in the future. The hydrogen source to operate the PEMFC system is methanol, which needs two parts of methanol reforming reaction and preferential oxidation (PROX) for the hydrogen fuel process in the combined operation PEMFC system. With the optimized methanol steam reforming condition, we tested PROX reactions in various operation temperature from 170 to 270 ℃ to investigate CO concentration data in the reformed gases. Using these different CO concentration, PEMFC performances are achieved at the combined system. Pt/C and Ru promoted Pt/C were catalysts were used for the anode to compare the stability in CO contained gases. The alloy catalyst of PtRu/C shows higher performance and better resistance to CO than the Pt/C at even high CO amount of 200 ppm, indicating a promotion not only to the activity but also to the CO tolerance. Furthermore, in a system point of view, there is a fluctuation in the PEMFC operation due to the unstable fuel supply. Therefore, we also modified the methanol reforming by a scaled up reactor and pressurization to produce steady operation of PEMFC. The optimized system with the methanol reformer and PEMFC shows a stable performance for a long time, which is providing a valuable data for the PEMFC commercialization.

메조페이스 핏치로부터 균질한 다공성 탄소 제조 및 이를 이용한 직접 메탄올 연료전지의 촉매 담지체 특성 (Preparation of Uniform Porous Carbon from Mesophase Pitch and Its Characteristics of Catalyst Support for the Direct Methanol Fuel Cell)

  • 남기돈;김태진;김상경;이병록;백동현;유승곤;정두환
    • 공업화학
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    • 제17권2호
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    • pp.223-228
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    • 2006
  • 직접 메탄올 연료전지에서 촉매 담지체로서 세공 크기별 균질한 다공성 탄소는 메조페이스 핏치와 졸-겔법으로 직접 합성한 구형 실리카를 이용하여 제조하였다. Tetrahydrofuran (THF)에 용해된 핏치와 메탄올에 분산된 구상의 실리카를 혼합하고 탄화한 후에 5 M NaOH로 실리카를 식각하여 다공성 탄소를 만들었다. 이 다공성탄소의 비표 면적은 사용된 구형 실리카의 입자 크기가 작을수록 증가하였으며, $14.7{\sim}87.7m^2/g$ 범위를 나타내었다. 평균 기공 직경 또한 사용된 실리카 입자크기에 따라 50~550 nm로 다양하게 나타났다. 다공성 탄소 담지체에 백금과 루테늄을 담지시키기 위해 액상환원법을 사용하였고, 60 wt% 백금-루테늄이 담지된 촉매의 전기 산화 활성 및 전극 성능 특성은 순환 전압 전류법과 단위전지 시험으로 평가하였다. 본 실험 범위 중 50 nm 실리카를 이용하여 제조한 백금-루테늄/다공성탄소의 경우(60 wt% Pt-Ru/porous carbon), 순환 전압 전류법 시험에서 0.4 V에서의 전류 밀도 값이 $123mA/cm^2$가 측정되었고, 단위전지 성능 시험에서는 최대 전력 밀도 값이 $60^{\circ}C$$80^{\circ}C$, 산소분위기에서 각각 105, $162mW/cm^2$를 나타내었다.

$RuO_2$박막을 이용한 박막 슈퍼캐패시터의 제작 및 분석 (Fabrication and charaterization of $RuO_2$based thin film supercapacitor)

  • 임재홍;최두진;전은정;남성철;조원일;윤영수
    • 한국전기전자재료학회:학술대회논문집
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    • 한국전기전자재료학회 2000년도 하계학술대회 논문집
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    • pp.920-923
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    • 2000
  • All solid-state thin film supercapacitor(TFSC) based on $RuO_2$ electrode was fabricated. Ruthenium oxide$(RuO_2)$ thin film was deposited on Pt/Ti/Si subsrate by d.c. magnetron sputtering. LiPON(lithium phosphorus oxynitride) thin film were deposited by r.f. reactive sputtering. X-ray diffraction patterns of $RuO_2$ and LiPON films revealed that crystal structures of both films were amorphous. To decrease resistivity of $RuO_2$ thin film, $RuO_2$ thin film was deposited with $H_2O$ vapor. In order to decide the maximum ionic conductivity, the LiPON films were prepared by various sputtering condition. The maximum ionic conductivity was $9.5\times{10}^7S/cm$. A charge-discharge measurements showed the capacity of $3\times{10-2}\;F/cm^2-\mu{m}$ for the as-fabricated TFSC. The discharging efficiency was decreased after 500 cycles by 40 %.

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산화제 생성율이 높은 촉매성 산화물 전극(DSA)의 개발에 관한 연구(I) (A Study on the Preparation of the Dimensionally Stable Anode(DSA) with High Generation Rate of Oxidants(I))

  • 김동석;박영식
    • 한국환경과학회지
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    • 제18권1호
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    • pp.49-60
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    • 2009
  • Fabrication and oxidants formation of 1 and 2 component metal oxide electrode, which is known to be so effective to destruct non-biodegradable organics in wastewater, were studied. Five electrode materials (Ru, Pt, Sn, Sb and Gd) were used for the 1 and 2 component electrode. The metal oxide electrode was prepared by coating the electrode material on the surface of the titanium mesh and then thermal oxidation at $500^{\circ}C$ for 1 h. The removed RhB per 2 min and unit W for one component electrode decreased in the following sequences: Ru/Ti>Sb/Ti>Pt/Ti>Gd/Ti>Sn/Ti. The concentration of oxidants generated in 1 and 2 component electrodes was in the order of: $ClO_2$> free Cl>$H_2O_2>O_3$. OH radical was not generated from in entire one and two component electrodes. RhB degradation rate and generated oxidants of the Ru-Sn=9:1 electrode was higher than that of the two component electrode. The exact relationship between the removal of RhB and the generated oxidants concentration was not obvious. However, it was assumed that electrode with high RhB decolorization had high oxidant concentration.