Strain Engineering to Enhance the Electrooxidation Performance of Atomic-Layer Pt on Intermetallic Pt3Ga

被引:244
作者
Feng, Quanchen [1 ]
Zhao, Shu [2 ]
He, Dongsheng [3 ]
Tian, Shubo [1 ]
Gu, Lin [4 ]
Wen, Xiaodong [5 ]
Chen, Chen [1 ]
Peng, Qing [1 ]
Wang, Dingsheng [1 ]
Li, Yadong [1 ]
机构
[1] Tsinghua Univ, Dept Chem, Beijing 100084, Peoples R China
[2] Beijing Univ Technol, Beijing Guyue New Mat Res Inst, Beijing 100124, Peoples R China
[3] South Univ Sci & Technol China, Mat Characterizat & Preparat Ctr, Shenzhen 518055, Peoples R China
[4] Chinese Acad Sci, Inst Phys, Beijing 100190, Peoples R China
[5] Chinese Acad Sci, Inst Coal Chem, State Key Lab Coal Convers, Taiyuan 030001, Shanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
OXYGEN REDUCTION REACTION; SURFACE STRAIN; CATALYSTS; ELECTROCATALYSTS; NANOPARTICLES; MASS; NANOCRYSTALS; DURABILITY; NANOWIRES; ELECTRODE;
D O I
10.1021/jacs.7b13612
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Strain engineering has been a powerful strategy to finely tune the catalytic properties of materials. We report a tensile-strained two-to-three atomic-layer Pt on intermetallic Pt3Ga (AL-Pt/Pt3Ga) as an active electrocatalyst for the methanol oxidation reaction (MOR). Atomic-resolution high-angle annular dark-field scanning transmission electron microscopy characterization showed that the AL-Pt possessed a 3.2% tensile strain along the [001] direction while having a negligible strain along the [100]/[010] direction. For MOR, this tensile-strained AL-Pt electrocatalyst showed obviously higher specific activity (7.195 mA cm(-2)) and mass activity (1.094 mA/mu g(pt)) than those of its unstrained counterpart and commercial Pt/C catalysts. Density functional theory calculations demonstrated that the tensile-strained surface was more energetically favorable for MOR than the unstrained one, and the stronger binding of OH* on stretched AL-Pt enabled the easier removal of CO*.
引用
收藏
页码:2773 / 2776
页数:4
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