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Received August 4, 2010
Accepted January 31, 2011
- 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.
Copyright © KIChE. All rights reserved.
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Optimization of physical parameters of solid oxide fuel cell electrode using electrochemical model
Department of Chemical and Biological Engineering, Korea University, Seoul 136-713, Korea
kimsh@korea.ac.kr
Korean Journal of Chemical Engineering, September 2011, 28(9), 1844-1850(7), 10.1007/s11814-011-0026-4
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Abstract
To enhance the performance of anode-supported solid oxide fuel cell (SOFC), an electrochemical model has been developed in this study. The Butler-Volmer equation, Ohm’s law and dusty-gas model are incorporated to predict the activation, ohmic and concentration overpotentials, respectively. The optimal cell microstructure and operating parameters for the best current-voltage (J-V) characteristics have been sought from the information of the exchange_x000D_
current density and gas diffusion coefficients. As the cell temperature rises, the activation and ohmic overpotentials decrease, whereas the concentration overpotential increases due to the considerable reduction of gas density at the elevated temperature despite the increased diffusion coefficient. Also, increasing the hydrogen molar fraction and operating pressure can further augment the maximum cell output. Since there exists an optimum electrode pore size and porosity for maximum cell power density, the graded electrode has newly been designed to effectively reduce both the activation and concentration overpotentials. The results exhibit 70% improved cell performance than the case with a non-graded electrode. This electrochemical model will be useful to simply understand overpotential features and devise the strategy for optimal cell design in SOFC systems.
Keywords
References
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Hernandez-Pacheco E, Singh D, Hutton PN, Patel N, Mann MD, J. Power Sources, 138(1-2), 174 (2004)
Kakac S, Pramuanjaroenkij A, Zhou XY, Int. J. Hydrog. Energy., 32, 761 (2007)
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Sunde S, J. Electroceram., 5(2), 153 (2000)
Divisek J, Jung R, Vinke IC, J. Appl. Electrochem., 29(2), 165 (1999)
Chan SH, Xia ZT, J. Electrochem. Soc., 148(4), A388 (2001)
Chan SH, Khor KA, Xia ZT, J. Power Sources, 93(1-2), 130 (2001)
Zhu HY, Kee RJ, J. Power Sources, 117(1-2), 61 (2003)
Lehnert W, Meusinger J, Thom F, J. Power Sources, 87(1-2), 57 (2000)
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Achenbach E, J. Power Sources., 49, 333 (1994)
Yakabe H, Ogiwara T, Hishinuma M, Yasuda I, J. Power Sources, 102(1-2), 144 (2001)
Iwata M, Hikosaka T, Morita M, Iwanari T, Ito K, Onda K, Esaki Y, Sakaki Y, Nagata S, Solid State Ion., 132(3-4), 297 (2000)
Deng XH, Petric A, J. Power Sources, 140(2), 297 (2005)
Suwanwarangkul R, Croiset E, Fowler MW, Douglas PL, Entchev E, Douglas MA, J. Power Sources, 122(1), 9 (2003)
Chan SH, Khor KA, Xia ZT, J. Power Sources, 93(1-2), 130 (2001)
Zhu HY, Kee RJ, J. Power Sources, 117(1-2), 61 (2003)
Ferguson JR, Fiard JM, Herbin R, J. Power Sources., 58, 109 (1996)
Ringuede A, Bronine D, Frade JR, Solid State Ion., 146(3-4), 219 (2002)
Chan SH, Xia ZT, J. Appl. Electrochem., 32(3), 339 (2002)
Ni M, Leung MKH, Leung DYC, J. Power Sources, 168(2), 369 (2007)
Kong JR, Sun KN, Zhou DR, Zhang NQ, Mu J, Qiao JS, J. Power Sources, 166(2), 337 (2007)
Ni M, Leung MKH, Leung DYC, Energy Conv. Manag., 48(5), 1525 (2007)
Song TW, Sohn JL, Kim JH, Kim TS, Ro ST, Suzuki K, J. Power Sources, 142(1-2), 30 (2005)
Costamagna P, Magistri L, Massardo AF, J. Power Sources, 96(2), 352 (2001)
Petruzzi L, Cocchi S, Fineschi F, J. Power Sources, 118(1-2), 96 (2003)
Pfafferodt M, Heidebrecht P, Stelter M, Sundmacher K, J. Power Sources, 149, 53 (2005)
Ringuede A, Bronine D, Frade JR, Solid State Ionics., 146, 219 (20)