过电位
催化作用
甲酸
法拉第效率
乙醇
选择性
化学
二氧化碳电化学还原
结合能
电催化剂
无机化学
电化学
物理化学
一氧化碳
有机化学
电极
物理
核物理学
作者
Zhihui Liu,Hai Liu,Jianping Li,Yichen Meng,Xiao Wang,Tianxiang Yan,Qun Fan,Shi Nee Lou,Wenquan Cui,Sheng Zhang
标识
DOI:10.1002/cctc.202301700
摘要
Abstract Renewable energy driven electrochemical carbon dioxide reduction (CO 2 RR) to alcohols provides an effective pathway for achieving carbon neutrality and sustainable development. However, it is challenging to convert CO 2 into ethanol due to the sluggish C−C coupling and complex 12 electron/proton transferred process, which has been achieved mainly on Cu catalysts but with poor selectivity. Herein, In 2 O 3 catalysts were doped with small amount of Pd and exhibited high activity for CO 2 RR to ethanol with a high Faradaic efficiency (50.7 %) at low overpotential. The introduction of Pd promotes the transformation of reaction products from formic acid to ethanol by modulating the binding strength of *CO intermediates. The in‐situ ATR‐SEIRAS and DFT calculations proved that the formation of Pd−O−In could modulate the binding strength of *CO and enhanced its coverage, thus facilitating C−C coupling step towards ethanol. This study may provide a new strategy to the generation of high value‐added products from CO 2 over Non‐Cu‐based catalysts.
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