Performance enhancement in vanadium redox flow battery using platinum-based electrocatalyst synthesized by polyol process

被引:74
作者
Jeong, Sanghyun [1 ]
Kim, Sunhoe [2 ]
Kwon, Yongchai [1 ]
机构
[1] Seoul Natl Univ Sci & Technol, Grad Sch Energy & Environm, Seoul 139743, South Korea
[2] Sangji Univ, Dept New Energy & Resource Engn, Gangwon Do 220702, Wonju Si, South Korea
关键词
Vanadium redox flow battery; Polyol Pt/C catalyst; Charge-discharge performance; Electron transfer rate constant; Laviron's equation; CARBON NANOTUBE; GRAPHITE FELT; ELECTRODES; COUPLE; CELL; V(IV)/V(V); VO2+/VO2+; MECHANISM; OXIDATION;
D O I
10.1016/j.electacta.2013.10.011
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Sluggish reaction rate of [VO](2+)/[VO2](+) redox couple is an obstacle to be addressed in vanadium redox flow battery (VRFB). To improve the slow reaction rate, Pt/C catalyst synthesized by polyol method is suggested. Its catalytic activity, reaction reversibility and charge-discharge performance are evaluated by half cell and single cell tests, while its crystal structure, particle size and particle distribution are measured by XRD and TEM. The XRD and TEM measurements show the polyol Pt/C catalyst has larger electrochemically active surface (EAS) area and smaller particle size than commercial Pt/C catalyst. When catalytic activities of all the catalysts are estimated, the Pt-included catalysts demonstrate high peak current ratio, small peak potential difference and high electron transfer rate constant, confirming that their catalytic activity and reaction reversibility are excellent. In charge-discharge performance tests, the catalysts indicate high efficiencies as well as low overpotential and internal resistance. Excellent performances of the Pt-included catalysts are attributed to positively charged Pts that serve as active sites for activating [VO](2+)/[VO2](+). reaction. Indeed, adoption of the Pt-included catalysts, especially, use of the polyol Pt/C consisting of uniform and small particles helps improve performance of VRFB. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:439 / 447
页数:9
相关论文
共 34 条
[1]   Size-selected synthesis of PtRu nano-catalysts: Reaction and size control mechanism [J].
Bock, C ;
Paquet, C ;
Couillard, M ;
Botton, GA ;
MacDougall, BR .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (25) :8028-8037
[2]   Evaluation of electrolytes for redox flow battery applications [J].
Chakrabarti, M. H. ;
Dryfe, R. A. W. ;
Roberts, E. P. L. .
ELECTROCHIMICA ACTA, 2007, 52 (05) :2189-2195
[3]   Analysis of the Oxidation of the V(II) by Dissolved Oxygen Using UV-Visible Spectrophotometry in a Vanadium Redox Flow Battery [J].
Choi, Nak Heon ;
Kwon, Soon-Kwan ;
Kim, Hansung .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2013, 160 (06) :A973-A979
[4]   Redox flow cells for energy conversion [J].
de Leon, C. Ponce ;
Frias-Ferrer, A. ;
Gonzalez-Garcia, J. ;
Szanto, D. A. ;
Walsh, F. C. .
JOURNAL OF POWER SOURCES, 2006, 160 (01) :716-732
[5]   A REVIEW OF MATHEMATICAL-MODELING OF THE ZINC BROMINE FLOW CELL AND BATTERY [J].
EVANS, TI ;
WHITE, RE .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1987, 134 (11) :2725-2733
[6]  
Folkesson B., 1989, INORG CHIM ACTA, V162, P3514
[7]   Influence of Fenton's reagent treatment on electrochemical properties of graphite felt for all vanadium redox flow battery [J].
Gao, Chao ;
Wang, NanFang ;
Peng, Sui ;
Liu, SuQin ;
Lei, Ying ;
Liang, XinXing ;
Zeng, ShanShan ;
Zi, HuiFang .
ELECTROCHIMICA ACTA, 2013, 88 :193-202
[8]   Study of the mechanism of the vanadium 4+/5+redox reaction in acidic solutions [J].
Gattrell, M ;
Park, J ;
MacDougall, B ;
Apte, J ;
McCarthy, S ;
Wu, CW .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2004, 151 (01) :A123-A130
[9]   Investigation of Active Electrodes Modified with Platinum/Multiwalled Carbon Nanotube for Vanadium Redox Flow Battery [J].
Huang, Rong-Hsin ;
Sun, Chung-Hsing ;
Tseng, Tung-mo ;
Chao, Wen-kai ;
Hsueh, Kan-Lin ;
Shieu, Fuh-Sheng .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2012, 159 (10) :A1579-A1586
[10]  
Hyun K, 2013, INT J ELECTROCHEM SC, V8, P11752