Enhanced electrocatalytic performance of Pt monolayer on nanoporous PdCu alloy for oxygen reduction

被引:10
|
作者
Hou, Linxi [2 ]
Qiu, Huajun [1 ]
机构
[1] Shandong Univ, Sch Chem & Chem Engn, Jinan 250100, Peoples R China
[2] Ningbo Univ, Sch Mat Sci & Chem Engn, Ningbo 315211, Zhejiang, Peoples R China
关键词
Dealloying; Electrocatalyst; Fuel cell; ELECTROLYTE FUEL-CELLS; DEALLOYED PT-CU; CATALYTIC-ACTIVITY; STABILITY; SURFACE; NANOPARTICLES; ELECTROOXIDATION; METHANOL; ORR; AU;
D O I
10.1016/j.jpowsour.2012.05.064
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
By selectively dealloying Al from PdxCu20-xAl80 ternary alloys in 1.0 M NaOH solution, nanoporous PdCu (np-PdCu) alloys with different Pd:Cu ratios are obtained. By a mild electrochemical dealloying treatment, the np-PdCu alloys are facilely converted into np-PdCu near-surface alloys with a nearly pure-Pd surface and PdCu alloy core. The np-PdCu near-surface alloys are then used as substrates to fabricate core-shell catalysts with a Pt monolayer as shell and np-PdCu as core by a Cu-underpotential deposition-Pt displacement strategy. Electrochemical measurements demonstrate that the Pt monolayer on np-Pd1Cu1 (Pt/np-Pd1Cu1) exhibits the highest Pt surface-specific activity towards oxygen reduction, which is similar to 5.8-fold that of state-of-the-art Pt/C catalyst. The Pt/np-Pd1Cu1 also shows much enhanced stability with similar to 78% active surface retained after 10,000 cycles (0.6-1.2 V vs. RHE). Under the same condition, the active surface of Pt/C drops to similar to 28%. (c) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:28 / 32
页数:5
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