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Received December 13, 2004
Accepted March 14, 2005
- This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/bync/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
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Effect of Temperature, Oxidant and Catalyst Loading on the Performance of Direct Formic Acid Fuel Cell
Jeong Soo Kim
Jae Keun Yu
Hyo Song Lee
Jin Yong Kim
Young Chun Kim1
Jong Hee Han1
In Hwan Oh1
Young Woo Rhee†
Department of Chemical Engineering, Chungnam National University, 220, Gung-dong, Yuseong-gu, Daejeon 305-764, Korea 1Fuel Cell Research Center, Korea Institute of Science and Technology, 39-1, Hawolgok-dong, Sungbuk-gu, Seoul 136-791, Korea
Korean Journal of Chemical Engineering, September 2005, 22(5), 661-665(5), 10.1007/BF02705779
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Abstract
We investigated the effect of temperature, oxidant and catalyst loading on the performance of direct formic acid fuel cell (DFAFC). When oxidant was changed from air to oxygen, the power density was increased to 17.3mW/cm2 at 25 ℃. The power density of DFAFC operated with oxygen showed a maximum value of 40.04 mW/cm2 with the temperature rise from room temperature to 70 ℃. The highest power density of DFAFC using air was observed for Pt-Ru black catalyst with loading of 8 mgPt/cm2 at room temperature. At 70 ℃; however, the performance of catalyst with the loading of 4mgPt/cm2 was higher than that of 8 mgPt/cm2. The DFAFC, operated with oxygen and catalyst of 4 mgPt/cm2 loading, showed the best performance at all temperature range. The enhancement of cell performance with an increase of catalyst loading is believed to come from an increase of catalyst active sites. However, operated at higher temperature or with oxygen, the cell with higher catalyst loading showed lower performance than expected. It is speculated that the thick catalyst layer inhibits the proton transport.
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Ha S, Adams B, Masel RI, J. Power Sources, 128(2), 119 (2004)
Ha S, Rice CA, Masel RI, Wieckowski A, J. Power Sources, 112(2), 655 (2002)
Heinzel A, Barragan VM, J. Power Sources, 84(1), 70 (1999)
Jung DH, Prospect. Ind. Chem., 7(2), 14 (2004)
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)
Lee JH, Won J, Polym. Sci. Technol., 14(4), 418 (2003)
Lee SJ, Mukerjee S, McBreen J, Rho YW, Kho YT, Lee TH, Electrochim. Acta, 43(24), 3693 (1998)
Nakagawa N, Xiu Y, J. Power Sources, 118(1-2), 248 (2003)
Park GG, Sohn YJ, Yang TH, Yoon YG, Lee WY, Kim CS, J. Power Sources, 131(1-2), 182 (2004)
Reike PC, Vanderborgh NE, J. Membr. Sci., 32, 313 (1987)
Rhee YW, Ha SY, Masel RI, J. Power Sources, 117(1-2), 35 (2003)
Rice C, Ha RI, Masel RI, Waszczuk P, Wieckowski A, Barnard T, J. Power Sources, 111(1), 83 (2002)
Rice C, Ha S, Masel RI, Wieckowski A, J. Power Sources, 115(2), 229 (2003)
Son JE, Korean Chem. Eng. Res., 42(1), 1 (2004)
Yang TH, Park GG, Pugazhendhi P, Lee WY, Kim CS, Korean J. Chem. Eng., 19(3), 417 (2002)
Yoon WL, Park JW, Rhee YW, Han MW, Jeong JH, Park JS, Jung H, Lee HT, Kim CS, HWAHAK KONGHAK, 41(3), 389 (2003)
Zhu YM, Ha SY, Masel RI, J. Power Sources, 130(1-2), 8 (2004)