双金属片
催化作用
格式化
铜
法拉第效率
电化学
可逆氢电极
材料科学
电极
化学工程
无机化学
化学
工作电极
冶金
有机化学
物理化学
工程类
作者
Wenshuang Lou,Luwei Peng,Ruinan He,Yuyu Liu,Jinli Qiao
标识
DOI:10.1016/j.jcis.2021.08.080
摘要
Electrochemical reduction of CO2 to fuels and chemicals is an effective way to reduce greenhouse gas emissions and alleviate the energy crisis, but the highly active catalysts necessary for this reaction under mild conditions are still rare. In this work, we grew CuBi bimetallic catalysts on derived copper foam substrates by co-electrodeposition, and then investigated the correlation between co-electrodeposition potential and electrochemical performance in CO2-to-formate conversion. Results showed that the bimetallic catalyst formed at a low potential of - 0.6 V vs. AgCl/Ag electrode achieved the highest formate Faradaic efficiency (FEformate) of 94.4% and a current density of 38.5 mA/cm2 at a low potential of - 0.97 V vs. reversible hydrogen electrode (RHE). Moreover, a continuous-flow membrane electrode assembly reactor also enabled the catalyst to show better performance (a FEformate of 98.3% at 56.6 mA/cm2) than a traditional H-type reaction cell. This work highlights the vital impact of co-electrodeposition potential on catalyst performance and provides a basis for the modulated growth of bimetallic catalysts on substrates. It also shows the possibility of preparing Bi-based catalysts with no obvious decrease in catalytic activity that have been partially replaced with more economic copper.
科研通智能强力驱动
Strongly Powered by AbleSci AI