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Sulfonation of carbon-nanotube supported platinum catalysts for polymer electrolyte fuel cells
被引:97
作者:
Du, C. Y.
[1
]
Zhao, T. S.
[1
]
Liang, Z. X.
[1
]
机构:
[1] Hong Kong Univ Sci & Technol, Dept Mech Engn, Kowloon, Hong Kong, Peoples R China
关键词:
polymer electrolyte fuel cell;
Pt/CNT catalyst;
sulfonation;
thermal decomposition;
in situ radical polymerization;
D O I:
10.1016/j.jpowsour.2007.10.016
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
Sulfonic acid groups were grafted onto the surface of carbon-nanotube supported platinum (Pt/CNT) catalysts to increase platinum utilization in polymer electrolyte fuel cells (PEFCs) by both thermal decomposition of ammonium sulfate and in situ radical polymerization of 4-styrenesulfonate. The resultant sulfonated Pt/CNT catalysts were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), Fourier transform infrared (FTIR) spectrometry, thermal gravimetric analysis (TGA) and electrochemical methods. The electrodes with the Pt/CNT catalysts sulfonated by the in situ radical polymerization of 4-styrenesulfonate exhibited better performance than did those with the unsulfortated counterparts, mainly because of the easier access with protons and well dispersed distribution of the sulfonated Pt/CNT catalysts, indicating that sulfonation is an efficient approach to improve performance and reduce cost for the Pt/CNT-based PEFCs. The electrodes with the Pt/CNT catalysts sulfonated by the thermal decomposition of ammonium sulfate, however, did not yield the expected performance as in the case of carbon black supported platinum (Pt/C) catalysts, probably due to the significant agglomeration of platinum particles on the CNT surface at high temperatures, indicating that the Pt/CNT catalysts are more sensitive to temperature than the Pt/C catalysts. (c) 2007 Elsevier B.V. All rights reserved.
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页码:9 / 15
页数:7
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