Electrochemical CO2 Reduction on Gas Diffusion Electrodes: Enhanced Selectivity of In-Bi Bimetallic Particles and Catalyst Layer Optimization through a Design of Experiment Approach

被引:15
|
作者
Philips, Matthew F. [1 ,2 ]
Pavesi, Davide [1 ,2 ]
Wissink, Tim [3 ]
Figueiredo, Marta C. [3 ]
Gruter, Gert-Jan M. [1 ,4 ]
Koper, Marc T. M. [2 ]
Schouten, Klaas Jan P. [1 ,5 ]
机构
[1] Avantium Chem BV, NL-1014 BV Amsterdam, Netherlands
[2] Leiden Univ, Leiden Inst Chem, NL-2300 RA Leiden, Netherlands
[3] Eindhoven Univ Technol, Inorgan Mat & Catalysis, NL-5600 MB Eindhoven, Netherlands
[4] Univ Amsterdam, Vant Hoff Inst Mol Sci, NL-1090 GD Amsterdam, Netherlands
[5] Teijin Aramid BV, Tivolilaan 50, NL-6824 BW Arnhem, Netherlands
关键词
electrochemistry; CO2; reduction; gas diffusion electrode; bimetallic particles; catalyst optimization; formate; CARBON-DIOXIDE REDUCTION; METAL-ELECTRODES; FORMATE;
D O I
10.1021/acsaem.1c03156
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
CO2 electroreduction to formate powered by renewable energy is an attractive strategy to recycle carbon. Electrode materials showing high selectivity for formate at high current densities are post-transition metals such as Sn, In, Pb, Hg, and Bi. Scaling up the CO2 electroreduction technology to industrial size will require, among other things, maximization of selectivity at high current densities. We show here that InBi electrocatalysts provide enhanced selectivity compared to pure In and Bi and that a proper formulation of the catalyst layer can have a profound impact on the performance of gas diffusion electrode electrolyzers. The best performing electrodes screened in this study show nearly 100% current efficiency at current densities up to 400 mA cm(-2) for 2 h. Additionally, one electrode was shown to operate at a current density of 200 mA cm(-2) for 48 h at a current efficiency of 85% and remained operating with a current efficiency above 50% for 124 h.
引用
收藏
页码:1720 / 1730
页数:11
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