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Received August 28, 2006
Accepted November 14, 2006
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Preparation of Pt-Pd catalysts for direct formic acid fuel cell and their characteristics
Ki Ho Kim
Jae-Keun Yu1
Hyo Song Lee2
Jae Ho Choi
Soon Young Noh
Soo Kyung Yoon3
Chang-Soo Lee
Taek-Sung Hwang
Young Woo Rhee†
Department of Chemical Engineering, Chungnam National University, Daejeon 305-764, Korea 1Korea Institute of Footwear and Leather Technology, Busan 614-100, Korea 2Korea Environment and Resources Corperation, Incheon 404-170, Korea 3Netpreneur Co., Ltd., Seongnam 463-870, Korea
Korean Journal of Chemical Engineering, May 2007, 24(3), 518-521(4), 10.1007/s11814-007-0091-x
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Abstract
Pt-Pd catalysts were prepared by using the spontaneous deposition method and their characteristics were analyzed in a direct formic acid fuel cell (DFAFC). Effects of calcination temperature and atmosphere on the cell performance were investigated. The calcination temperatures were 300, 400 and 500 ℃ and the calcination atmospheres were air and nitrogen. The fuel cell with the catalyst calcined at 400 ℃ showed the best cell performance of 58.8mW/cm2. The effect of calcination atmosphere on the overall performance of fuel cell was negligible. The fuel cell with catalyst calcined at air atmosphere showed high open circuit potential (OCP) of 0.812 V. Also the effects of anode and cathode catalyst loadings on the DFAFC performance using Pt-Pd (1 : 1) catalyst were investigated to optimize the catalyst loading. The catalyst loading had a significant effect on the fuel cell performance. Especially, the fuel cell with anode catalyst loading of 4mg/cm2 and cathode catalyst loading of 5mg/cm2 showed the best power density of 64.7mW/cm2 at current density of 200 mA/cm2.
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References
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Cheng X, Peng C, You MD, Liu L, Zhang Y, Fan QB, Electrochim. Acta, 51(22), 4620 (2006)
Rice C, Ha S, Masel RI, Wieckowski A, J. Power Sources, 115(2), 229 (2003)
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Morlang A, Neuhausen U, Klementiev KV, Schutze FW, Miehe G, Fuess H, Lox ES, Appl. Catal. B: Environ., 60(3-4), 191 (2005)
Kim T, Takahashi M, Nagai M, Kobayashi K, Electrochim. Acta, 50(2-3), 817 (2004)
Nakagawa N, Xiu Y, J. Power Sources, 118(1-2), 248 (2003)
Kim JS, Ruy JK, Jung EM, Lee HS, Kim JY, Kim YC, Han JH, Oh IH, Rhee YW, Korean Chem. Eng. Res., 42(5), 630 (2004)
Bae B, Kho BK, Lim TH, Oh IH, Hong SA, Ha HY, J. Power Sources, 158(2), 1256 (2006)
Rice C, Ha RI, Masel RI, Waszczuk P, Wieckowski A, Barnard T, J. Power Sources, 111(1), 83 (2002)
Kim JS, Yu JK, Lee HS, Kim JY, Kim YC, Han JH, Oh IH, Rhee YW, Korean J. Chem. Eng., 22(5), 661 (2005)
Sauk J, Byun J, Kang Y, Kim H, Korean J. Chem. Eng., 22(4), 605 (2005)
Rhee YW, Ha SY, Masel RI, J. Power Sources, 117(1-2), 35 (2003)
Lee S, Kim D, Lee J, Chung ST, Ha HY, Korean J. Chem. Eng., 22(3), 406 (2005)
Choi JH, Jeong KJ, Dong Y, Han J, Lim TH, Lee JS, Sung YE, J. Power Sources, 163(1), 71 (2006)
Yang TH, Park GG, Pugazhendhi P, Lee WY, Kim CS, Korean J. Chem. Eng., 19(3), 417 (2002)
Cheng X, Peng C, You MD, Liu L, Zhang Y, Fan QB, Electrochim. Acta, 51(22), 4620 (2006)
Rice C, Ha S, Masel RI, Wieckowski A, J. Power Sources, 115(2), 229 (2003)
Waszczuk P, Barnard TM, Rice C, Masel RI, Wieckowski A, Electrochem. Commun., 4, 599 (2002)
Llorca MJ, Herrero E, Feliu JM, Aldaz A, J. Electroanal. Chem., 373(1-2), 217 (1994)
Attard GA, Bannister A, J. Electroanal. Chem., 300, 467 (1991)
Morlang A, Neuhausen U, Klementiev KV, Schutze FW, Miehe G, Fuess H, Lox ES, Appl. Catal. B: Environ., 60(3-4), 191 (2005)
Kim T, Takahashi M, Nagai M, Kobayashi K, Electrochim. Acta, 50(2-3), 817 (2004)
Nakagawa N, Xiu Y, J. Power Sources, 118(1-2), 248 (2003)
Kim JS, Ruy JK, Jung EM, Lee HS, Kim JY, Kim YC, Han JH, Oh IH, Rhee YW, Korean Chem. Eng. Res., 42(5), 630 (2004)
Bae B, Kho BK, Lim TH, Oh IH, Hong SA, Ha HY, J. Power Sources, 158(2), 1256 (2006)