High-Performance Pt-Co Nanoframes for Fuel-Cell Electrocatalysis

被引:198
作者
Chen, Shouping [1 ,3 ,4 ]
Li, Mufan [3 ]
Gao, Mengyu [1 ]
Jin, Jianbo [2 ]
van Spronsen, Matthijs A. [3 ]
Salmeron, Miquel B. [1 ,3 ]
Yang, Peidong [1 ,2 ,3 ,4 ]
机构
[1] Univ Calif Berkeley, Dept Mat Sci & Engn, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA
[3] Lawrence Berkeley Natl Lab, Mat Sci Div, Berkeley, CA 94720 USA
[4] Kavli Energy NanoSci Inst, Berkeley, CA 94720 USA
关键词
platinum-cobalt electrocatalyst; nanoframe; oxygen reduction reaction; methanol oxidation reaction; fuel cell; OXYGEN REDUCTION; ANISOTROPIC GROWTH; SEGREGATION; NANOWIRES; CATALYSTS;
D O I
10.1021/acs.nanolett.9b05251
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Pt-based alloy catalysts are promising candidates for fuel-cell applications, especially for cathodic oxygen reduction reaction (ORR) and anodic methanol oxidation reaction (MOR). The rational design of composition and morphology is crucial to promoting catalytic performances. Here, we report the synthesis of Pt-Co nanoframes via chemical etching of Co from solid rhombic dodecahedra. The obtained Pt-Co nanoframes exhibit excellent ORR mass activity in acidic electrolyte, which is as high as 0.40 A mg(Pt)(-1) initially and 0.34 A mg(Pt)(-1) after 10 000 potential cycles at 0.95 V-RHE. Furthermore, their MOR mass activity in alkaline media is up to 4.28 A mg(Pt)(-1) and is 4-fold higher than that of commercial Pt/C catalyst. Experimental studies indicate that the weakened binding of intermediate carbonaceous poison contributes to the enhanced MOR behavior. More impressively, the Pt-Co nanoframes also demonstrate remarkable stability under long-term testing, which could be attributed to the negligible electrochemical Co dissolution.
引用
收藏
页码:1974 / 1979
页数:6
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