Electrochemical CO2 Reduction Over Bimetallic Au-Sn Thin Films: Comparing Activity and Selectivity against Morphological, Compositional, and Electronic Differences

被引:12
作者
Chandrashekar, Sanjana [1 ]
Nesbitt, Nathan T. [1 ]
Smith, Wilson A. [1 ]
机构
[1] Delft Univ Technol, Mat Energy Convers & Storage MECS, Dept Chem Engn, NL-2629 HZ Delft, Netherlands
关键词
HIGH-PRESSURE CO2; CARBON-DIOXIDE; TIN ELECTRODES; NANOPARTICLES; ELECTROREDUCTION; FORMATE; PB;
D O I
10.1021/acs.jpcc.0c01894
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
Carbon dioxide can be electrochemically converted into feedstocks for many industrial processes, such as the manufacturing of synthetic fuels and chemicals. This work focuses on the structure-functionality relationship between Au, Sn, and bimetallic AuSn catalysts and their CO2 reduction performance in an H-Cell at varying current densities. X-Ray diffraction (XRD), X-ray photoemission spectroscopy (XPS), and atomic force microscopy (AFM) were used to determine the crystal structure, surface morphology, and composition of compositionally variant bimetallic thin films of Au-Sn before and after electrolysis. The electrochemical activity for each bimetallic film was measured in terms of electrode current and product selectivity as a function of applied current density and catalyst composition. The results of this work show that not all combinations of metals for CO2 reduction can improve catalyst activity toward a desired product and that a detailed material characterization can help in drawing structure-functionality relationships between a catalyst and its activity.
引用
收藏
页码:14573 / 14580
页数:8
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[11]   Isotopic effect on electrochemical CO2 reduction activity and selectivity in H2O- and D2O-based electrolytes over palladium [J].
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