过电位
催化作用
钯
格式化
甲酸
合理设计
法拉第效率
电合成
化学
电化学
电催化剂
二氧化碳电化学还原
无机化学
选择性
化学工程
有机化学
材料科学
一氧化碳
纳米技术
物理化学
电极
工程类
作者
Anna Klinkova,Phil De Luna,Cao‐Thang Dinh,Oleksandr Voznyy,Egor M. Larin,Moritz Tebbe,Edward H. Sargent
标识
DOI:10.1021/acscatal.6b01719
摘要
The electrochemical reduction of CO2 into renewable chemical products such as formic acid is an important and challenging goal. Traditional Pd catalysts suffer from CO poisoning, which leads to current density decay and short operating lifetimes. Here we explored the ability to control Pd nanoparticle surface morphology to amplify catalytic activity and increase stability in the electroreduction of CO2 to formate. Through computational studies we have elucidated trends in intermediate binding which govern the selectivity and catalytic activity. We then rationally synthesized Pd nanoparticles having an abundance of high-index surfaces to maximize electrocatalytic performance. This catalyst displays a record current density of 22 mA/cm2 at a low overpotential of −0.2 V with a Faradaic efficiency of 97%, outperforming all previous Pd catalysts in formate electrosynthesis. The findings presented in this work provide rational design principles which highlight morphological control of high-index surfaces for the effective and stable catalytic electroreduction of CO2 to liquid fuels.
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