ISSN: 0256-1115 (print version) ISSN: 1975-7220 (electronic version)
Copyright © 2024 KICHE. All rights reserved

Articles & Issues

Language
English
Conflict of Interest
In relation to this article, we declare that there is no conflict of interest.
Publication history
Received May 23, 2007
Accepted August 1, 2007
articles 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.

All issues

Electrochemical deposition of Pt nanoparticles on CNTs for fuel cell electrode

Korea Institute of Energy Research, Daejeon 305-343, Korea
Korean Journal of Chemical Engineering, May 2008, 25(3), 443-445(3), 10.1007/s11814-008-0075-5
downloadDownload PDF

Abstract

In order to increase the performance of fuel cell electrode, carbon nanotubes (CNTs) were used as support instead of conventional carbon black, and the Pt catalyst was synthesized by using electrochemical deposition (ECD) method which has recently been adopted as a synthetic tool of metal nanoparticles. CNTs used in this paper were grown directly on carbon paper by chemical vapor deposition (CVD) of acetylene. Highly dispersed and nano-sized Pt particles were electrochemically deposited on CNTs surface, which would simplify the manufacturing process of membrane-electrode-assembly (MEA). Pt particles on CNTs were investigated by SEM and TEM. The particle size of Pt is less than 2 nm, which is relatively small compared to that of conventional wet impregnated catalyst (2-8 nm). CO chemisorption results show that the amounts of catalytic sites are about three times larger in Pt/CNT prepared by ECD than those in conventional wet-impregnated one. The mass activity of the former catalyst for oxygen reduction is more than three times higher compared to that of the latter one.

References

Fazle Kibria AKM, Mo YH, Yun MH, Kim MJ, Nahm KS, Korean J. Chem. Eng., 18(2), 208 (2001)
Shajahan M, Mo YH, Nahm KS, Korean J. Chem. Eng., 20(3), 566 (2003)
Mu YY, Liang HP, Hu JS, Jiang L, Wan LJ, J. Phys. Chem. B, 109(47), 22212 (2005)
Li WZ, Wang X, Chen ZW, Waje M, Yan YS, J. Phys. Chem. B, 110(31), 15353 (2006)
Liu ZL, Lin XH, Lee JY, Zhang W, Han M, Gan LM, Langmuir, 18(10), 4054 (2002)
Planeix JM, Coustel N, Coq B, Brotons V, Kumbhar PS, Dutartre R, Geneste P, Bernier P, Ajayan PM, J. Am. Chem. Soc., 116(17), 7935 (1994)
He ZB, Chen JH, Liu DY, Tang H, Deng W, Kuang WF, Mater. Chem. Phys., 85(2-3), 396 (2004)
Guha A, Lu W, Zawodzinski TA, Schiraldi DA, Carbon, 45, 1506 (2007)

The Korean Institute of Chemical Engineers. F5, 119, Anam-ro, Seongbuk-gu, 233 Spring Street Seoul 02856, South Korea.
TEL. No. +82-2-458-3078FAX No. +82-507-804-0669E-mail : kiche@kiche.or.kr

Copyright (C) KICHE.all rights reserved.

- Korean Journal of Chemical Engineering 상단으로