Synthesis and Electrocatalytic Performance of Multi-Component Nanoporous PtRuCuW Alloy for Direct Methanol Fuel Cells

被引:24
作者
Chen, Xiaoting [1 ]
Wang, Hao [1 ]
Wang, Ying [1 ]
Bai, Qingguo [1 ]
Gao, Yulai [2 ]
Zhang, Zhonghua [1 ]
机构
[1] Shandong Univ, Sch Mat Sci & Engn, Key Lab Liquid Solid Struct Evolut & Proc Mat, Minist Educ, Jinan 250061, Peoples R China
[2] Shanghai Univ, Lab Microstruct, Shanghai 200436, Peoples R China
基金
中国国家自然科学基金;
关键词
direct methanol fuel cells; methanol oxidation; oxygen reduction reaction; dealloying; nanoporous alloys; OXYGEN REDUCTION REACTION; ETHANOL ELECTROOXIDATION; CATALYTIC-ACTIVITY; CARBON NANOTUBES; ANODE CATALYSTS; OXIDATION; NANOPARTICLES; PLATINUM; CO; RU;
D O I
10.3390/catal5031003
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
We have prepared a multi-component nanoporous PtRuCuW (np-PtRuCuW) electrocatalyst via a combined chemical dealloying and mechanical alloying process. The X-ray diffraction (XRD), transmission electron microscopy (TEM) and electrochemical measurements have been applied to characterize the microstructure and electrocatalytic activities of the np-PtRuCuW. The np-PtRuCuW catalyst has a unique three-dimensional bi-continuous ligament structure and the length scale is 2.0 +/- 0.3 nm. The np-PtRuCuW catalyst shows a relatively high level of activity normalized to mass (467.1 mA mg(Pt)(-1)) and electrochemically active surface area (1.8 mA cm(-2)) compared to the state-of-the-art commercial PtC and PtRu catalyst at anode. Although the CO stripping peak of np-PtRuCuW 0.47 V (vs. saturated calomel electrode, SCE) is more positive than PtRu, there is a 200 mV negative shift compared to PtC (0.67 V vs. SCE). In addition, the half-wave potential and specific activity towards oxygen reduction of np-PtRuCuW are 0.877 V (vs. reversible hydrogen electrode, RHE) and 0.26 mA cm(-2), indicating a great enhancement towards oxygen reduction than the commercial PtC.
引用
收藏
页码:1003 / 1015
页数:13
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