假电容
材料科学
铜
二氧化碳电化学还原
X射线光电子能谱
电催化剂
氢
无机化学
纳米技术
化学工程
催化作用
有机化学
超级电容器
电化学
一氧化碳
电极
化学
物理化学
工程类
冶金
作者
Juan‐Jesús Velasco‐Vélez,Axel Knop‐Gericke,Beatriz Roldán Cuenya,Robert Schlögl,Travis E. Jones
标识
DOI:10.1002/aenm.202400054
摘要
Abstract Electroreduction of CO 2 to value‐added products is a promising strategy for CO 2 reuse, where copper has a unique ability to produce oxygenates and C 2+ products. Unfortunately, the electronic factors making copper so unique are unknown, which limits the ability to design improved catalysts. By combining in situ surface‐sensitive X‐ray resonant photoelectron spectroscopy with density functional theory calculations, the complex electronic structure of copper is uncovered during the electrocatalytic reduction of CO 2 . It is found that the pseudocapacitive charging of copper, produced by the incorporation of protons and electrons into the subsurface, facilitates the activation of CO 2 , while simultaneously increasing the barrier for H‐H coupling. The net result is that cathodic pseudocapacitive charge suppresses the hydrogen evolution reaction and promotes the production of hydrocarbons and oxygenated products on copper. These results represent a new paradigm in the understanding of CO 2 reduction, highlighting the key role of pseudocapacitive charge in the reaction.
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