Cu@Pt catalysts prepared by galvanic replacement of polyhedral copper nanoparticles for polymer electrolyte membrane fuel cells

被引:31
|
作者
Wu, Meixia [1 ]
Wu, Xin [2 ]
Zhang, Lei [3 ]
Abdelhafiz, Ali [3 ]
Chang, Ikwhang [3 ]
Qu, Chong [3 ]
Jiang, Yangcheng [2 ]
Zeng, Jianhuang [2 ]
Alamgir, Faisal [3 ]
机构
[1] Shanxi Datong Univ, Coll Chem & Environm Engn, 5 Xingyun St, Datong 037009, Peoples R China
[2] South China Univ Technol, Sch Chem & Chem Engn, Guangdong Key Lab Fuel Cell Technol, Guangzhou 510641, Guangdong, Peoples R China
[3] Georgia Inst Technol, Sch Mat Sci & Engn, 771 Ferst Dr, Atlanta, GA 30332 USA
关键词
Cu@Pt; Galvanic replacement; Methanol oxidation; Oxygen reduction reaction; OXYGEN REDUCTION REACTION; CORE-SHELL NANOPARTICLES; LAYER-BY-LAYER; METHANOL OXIDATION; ELECTROCATALYTIC ACTIVITY; DISPLACEMENT REACTION; PLATINUM; SURFACE; GRAPHENE; NI;
D O I
10.1016/j.electacta.2019.03.111
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Polyhedral copper nanoparticles are prepared by a hydrothermal method, followed by galvanic replacement with platinum precursor in ethylene glycol to prepare bimetallic Cu@Pt electrocatalysts. The as-prepared bimetallic Cu@Pt catalyst are characterized by scanning electron microscopy, transmission electron microscopy, X-ray diffraction and inductive coupled plasma atomic emission spectrometer. The electrochemical properties of the resulted Cu@Pt electrocatalysts with different compositions are investigated for methanol oxidation reaction and oxygen reduction reaction. The bimetallic Cu@Pt electrocatalysts with low platinum loading demonstrate high Pt utilization efficiency in fuel cell reactions. The methanol oxidation reaction mass activity for Cu@Pt-8 catalyst is 791 A g(-1), 5.1 times higher than that of the commercial Pt/C. The highest oxygen reduction reaction mass activity is found for Cu@Pt-25 (93 A g(-1) at 0.9 V versus relative hydrogen electrode), which represents 61% enhancement relative to that of a commercial Pt/C (54 A g(-1)). It is believed that the superior performance of the as-prepared bimetallic Cu@Pt catalyst is mostly attributed to the improved Pt utilization and facilitated mass transport originating from the porous structure. (c) 2019 Elsevier Ltd. All rights reserved.
引用
收藏
页码:167 / 174
页数:8
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