Electroreduction of CO2 on Au(310)@Cu High-index Facets

被引:16
|
作者
Liang, Liang [1 ]
Feng, Quanchen [1 ]
Wang, Xingli [1 ]
Huebner, Jessica [1 ]
Gernert, Ulrich [2 ]
Heggen, Marc [3 ]
Wu, Longfei [1 ]
Hellmann, Tim [4 ]
Hofmann, Jan P. [4 ]
Strasser, Peter [1 ]
机构
[1] Tech Univ Berlin, Dept Chem, Chem Engn Div, Str 17 Juni 124, D-10623 Berlin, Germany
[2] Tech Univ Berlin, Inst Phys Sci & Informat Technol, Ctr Electron Microscopy ZELMI, Str 17 Juni 124, D-10623 Berlin, Germany
[3] Forschungszentrum Julich, Ernst Ruska Ctr Microscopy & Spect Electrons, D-52425 Julich, Germany
[4] Tech Univ Darmstadt, Dept Mat & Earth Sci, Surface Sci Lab, Otto Berndt Str 3, D-64287 Darmstadt, Germany
关键词
Electromethanation; High-Index Cu Facets; Operando Fourier Transform Infrared Spectroscopy; ELECTROCHEMICAL REDUCTION; CU; NANOCRYSTALS; GOLD; SELECTIVITY;
D O I
10.1002/anie.202218039
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The chemical selectivity and faradaic efficiency of high-index Cu facets for the CO2 reduction reaction (CO2RR) is investigated. More specifically, shape-controlled nanoparticles enclosed by Cu {hk0} facets are fabricated using Cu multilayer deposition at three distinct layer thicknesses on the surface facets of Au truncated ditetragonal nanoprisms (Au DTPs). Au DTPs are shapes enclosed by 12 high-index {310} facets. Facet angle analysis confirms DTP geometry. Elemental mapping analysis shows Cu surface layers are uniformly distributed on the Au {310} facets of the DTPs. The 7 nm Au@Cu DTPs high-index {hk0} facets exhibit a CH4 : CO product ratio of almost 10 : 1 compared to a 1 : 1 ratio for the reference 7 nm Au@Cu nanoparticles (NPs). Operando Fourier transform infrared spectroscopy spectra disclose reactive adsorbed *CO as the main intermediate, whereas CO stripping experiments reveal the high-index facets enhance the *CO formation followed by rapid desorption or hydrogenation.
引用
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页数:5
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