Understanding of Strain Effects in the Electrochemical Reduction of CO2: Using Pd Nanostructures as an Ideal Platform

被引:400
作者
Huang, Hongwen [1 ,2 ]
Jia, Huanhuan [1 ,2 ]
Liu, Zhao [1 ,2 ]
Gao, Pengfei [1 ,2 ]
Zhao, Jiangtao [1 ,2 ]
Luo, Zhenlin [1 ,2 ]
Yang, Jinlong [1 ,2 ]
Zeng, Jie [1 ,2 ]
机构
[1] Chinese Acad Sci, Hefei Natl Lab Phys Sci Microscale, Key Lab Strongly Coupled Quantum Matter Phys, Beijing 100864, Peoples R China
[2] Univ Sci & Technol China, Natl Synchrotron Radiat Lab, Dept Chem Phys, Anhua 230026, Peoples R China
基金
中国博士后科学基金;
关键词
adsorption energies; CO2; reduction; electrocatalysis; palladium; strain effects; CARBON-DIOXIDE; ELECTROCATALYTIC REDUCTION; ALLOY NANOCRYSTALS; LATTICE-STRAIN; CATALYSTS; ELECTROREDUCTION; ICOSAHEDRA; OXIDATION; FUEL;
D O I
10.1002/anie.201612617
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Tuning the surface strain of heterogeneous catalysts represents a powerful strategy to engineer their catalytic properties by altering the electronic structures. However, a clear and systematic understanding of strain effect in electrochemical reduction of carbon dioxide is still lacking, which restricts the use of surface strain as a tool to optimize the performance of electrocatalysts. Herein, we demonstrate the strain effect in electrochemical reduction of CO2 by using Pd octahedra and icosahedra with similar sizes as a well-defined platform. The Pd icosahedra/C catalyst shows a maximum Faradaic efficiency for CO production of 91.1% at -0.8 V versus reversible hydrogen electrode (vs. RHE), 1.7-fold higher than the maximum Faradaic efficiency of Pd octahedra/C catalyst at -0.7 V (vs. RHE). The combination of molecular dynamic simulations and density functional theory calculations reveals that the tensile strain on the surface of icosahedra boosts the catalytic activity by shifting up the d-band center and thus strengthening the adsorption of key intermediate COOH*. This strain effect was further verified directly by the surface valence-band photoemission spectra and electrochemical analysis.
引用
收藏
页码:3594 / 3598
页数:5
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