Liquid Crystalline Phase Templated Platinum Catalyst for Oxygen Reduction

被引:7
作者
Bauer, A. [1 ]
Wilkinson, D. P. [1 ]
Gyenge, E. L. [1 ]
Bizzotto, D. [2 ]
Ye, S. [3 ]
机构
[1] Univ British Columbia, Dept Chem & Biol Engn, Vancouver, BC V6T 1Z3, Canada
[2] Univ British Columbia, Dept Chem, Vancouver, BC V6T 1Z4, Canada
[3] Ballard Power Syst, Burnaby, BC V5J 5J8, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
ROTATING-DISK ELECTRODE; CARBON-SUPPORTED PLATINUM; FUEL-CELL; FILMS; ELECTROCATALYSIS; SURFACES; ALLOY; PERFORMANCE; MODEL;
D O I
10.1149/1.3176830
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The potentiostatic electrodeposition of platinum was carried out with a nonionic surfactant in the liquid crystalline phase acting as a templating agent. The electrochemically active Surface area of 0.4 mg cm(-2) unsupported Pt electrodeposited using a mixture of Brij 56 and n-heptane was increased by a factor of 2.7 compared to Pt deposited without structure-directing additives. The deposit morphology was studied by surface analysis (scanning electron microscopy, atomic force microscopy, and transmission electron microscopy). It was found that with the templating agent, the Pt nanoparticles with a 50 nut diameter had a mesoporous fine structure with pore diameters of 2-3 nm. Oxygen reduction experiments revealed a threefold increase in mass activity, and an improvement of the superficial Current density at 0.9 V vs reversible hydrogen electrode (RHE) front 2 X 10(-4) to 6 X 10(-4) A cm(geom)(-2) due to templating. The intrinsic specific activity of the templated Pt (i.e., current density normalized with respect to the active Pt area) was also improved at potentials more negative than 0.95 V vs RHE. The mesoporous structures Studied in this work served as a model for the design of highly active polymer electrolyte membrane fuel cell cathode catalyst layers. (C) 2009 The Electrochemical Society. [DOI: 10.1149/1.3176830] All rights reserved.
引用
收藏
页码:B1169 / B1174
页数:6
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