Highly stable platinum electrocatalysts for oxygen reduction formed using supercritical fluid impregnation

被引:17
作者
Ang, Shee-Yen
Walsh, Darren A. [1 ]
机构
[1] Univ Nottingham, Sch Chem, Nottingham NG7 2RD, England
基金
英国工程与自然科学研究理事会;
关键词
Fuel cell; Electrocatalysis; Supercritical carbon dioxide; Rotating-disk electrode; Oxygen reduction; POLYMER ELECTROLYTE MEMBRANE; PEM FUEL-CELL; CARBON-DIOXIDE; PARTICLE-SIZE; CATALYST UTILIZATION; NANOPARTICLES; DEPOSITION; DURABILITY; NANOTUBES; CATHODE;
D O I
10.1016/j.jpowsour.2009.10.097
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
A carbon-supported platinum electrocatalyst for the oxygen reduction reaction (ORR) in acidic medium was synthesised using supercritical fluid impregnation. The catalytic performance and electrochemical stability of this catalyst were studied using voltammetric and microscopic analysis. The results from these analyses were compared with those obtained using a Pt/C catalyst formed using a traditional wet chemical method (reduction of H-2 PtCl6 in aqueous solution using NaBH4). In the supercritical impregnation method, carbon black (Vulcan XC72R) was impregnated with (1,5-cyclooctadiene)dimethyl platinum(II), PtMe2COD, in supercritical carbon dioxide (scCO(2)) at 1200 p.s.i and 40 degrees C. After depressurisation, carbon-supported Pt nanoparticles were formed by thermally decomposing the adsorbed PtMe2COD. An accelerated stability test was performed, which revealed morphological changes in the electrocatalysts, which were significantly more pronounced in the Pt/C formed using the wet chemical method. Electrochemical analysis also showed that the Pt/C formed using wet chemistry lost a significant proportion of its electrochemical surface area after potential cycling, whereas that formed using scCO(2) did not. Furthermore, the Pt/C formed in scCO(2) retained its electrocatalytic activity to a significantly larger extent. The stability of the electrocatalysts formed using scCO(2) processing suggests that this approach may be promising for the fabrication of more stable fuel cell cathodes than are currently available. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:2557 / 2563
页数:7
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