3D carbon aerogel-supported PtNi intermetallic nanoparticles with high metal loading as a durable oxygen reduction electrocatalyst

被引:31
作者
Wang, Yameng [1 ,2 ]
Zou, Liangliang [1 ]
Huang, Qinghong [1 ]
Zou, Zhiqing [1 ]
Yang, Hui [1 ]
机构
[1] Chinese Acad Sci, Shanghai Adv Res Inst, Shanghai 201210, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100039, Peoples R China
基金
中国国家自然科学基金;
关键词
Platinum and nickel intermetallic; Graphene; Three-dimensional aerogel; Oxygen reduction reaction; Durability; PD3PT1 BIMETALLIC NANOPARTICLES; REDUCED GRAPHENE OXIDE; METHANOL FUEL-CELLS; ALLOY NANOPARTICLES; CATALYSTS; CO; OXIDATION; NANOTUBES; ELECTRODE; ROUTE;
D O I
10.1016/j.ijhydene.2017.09.008
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
Highly active and cost-effective oxygen reduction reaction (ORR) catalysts that have high metal loading and enhanced durability are desirable for the practical application in direct methanol fuel cells. Here, the preparation of a three dimensional (3D) carbon-based aerogel (CA) composed of graphene and multi-walled carbon nanotubes is reported and used as a support for an ordered PtNi intermetallic catalyst (O-PtNi/CA) with a metal loading of 80 wt %. X-ray diffraction and transmission electron microscopic measurements confirm the formation of highly dispersed ordered PtNi intermetallic nanoparticles with a mean particle size of ca. 15.0 +/- 1.0 nm. The as-prepared catalyst exhibits enhanced activity and durability for the ORR when compared to the Pt/C catalyst from BASF. The mass and specific activities of the ORR at 0.90 V on O-PtNi/CA is ca. 1.4 and 1.8 times higher, respectively, than that using the commercial PVC catalyst. After an accelerated stress test, the mean particle size of the O-PtNi/CA catalyst nearly kept unchanged. Both the improved activity and durability of the O-Pt-Ni/CA catalyst could be ascribed to the formation of an intermetallic compound, the uniform dispersion of PtNi nanoparticles, and the 3 D structure of the support. (C) 2017 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:26695 / 26703
页数:9
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