Graphene-supported platinum catalyst prepared with ionomer as surfactant for anion exchange membrane fuel cells

被引:21
|
作者
Zeng, L. [1 ]
Zhao, T. S. [1 ]
An, L. [1 ]
Zhao, G. [1 ]
Yan, X. H. [1 ]
Jung, C. Y. [1 ]
机构
[1] Hong Kong Univ Sci & Technol, Dept Mech & Aerosp Engn, Kowloon, Hong Kong, Peoples R China
关键词
Fuel cell; Anion exchange ionomer; Platinum nanoparticles; Electrocatalysts; High distribution; OXYGEN REDUCTION REACTION; POLYMER ELECTROLYTE MEMBRANES; METAL-FREE ELECTROCATALYSTS; CARBON NANOTUBES; FUNCTIONALIZED GRAPHENE; NANOPARTICLES; PERFORMANCE; OXIDATION; REMOVAL; ACID;
D O I
10.1016/j.jpowsour.2014.11.021
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
In this work, we have synthesized an ionomer-coated graphene-supported platinum catalyst for anion exchange membrane fuel cells. Unlike the common surfactant stabilized colloidal method, we employ a home-made anion exchange ionomer (AEI), namely quaternary ammonia poly (2, 6-dimethyl-1, 4-phenylene oxide) (QAPPO), as the surfactant. The AEI coated on reduced graphene oxide (rGO) surfaces serves as a stabilizer to anchor the platinum precursor on rGO surfaces due to electrostatic interactions. As a result, platinum nanoparticles (Pt NPs) can be easily deposited onto rGO surfaces with a uniform distribution. The remarkable feature of the present synthesis method is that the surfactant, the coated AEI, does not need to be removed from the catalyst, but serves as hydroxide-conductive paths in the catalyst layer, leading to enhanced triple phase boundaries. It is demonstrated that the use of the catalyst obtained with the present method enables a H-2/O-2 AEMFC to yield a peak power density of 264.8 mW cm(-2) at 60 degrees C, which is 30% higher than that produced from the same fuel cell but with the use of the catalyst synthesized by the conventional synthesis method. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:506 / 515
页数:10
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