法拉第效率
催化作用
铜
锑
选择性
材料科学
无机化学
合金
吸附
电解
电化学
化学工程
化学
冶金
物理化学
电解质
有机化学
电极
工程类
作者
Jiawei Li,Hongliang Zeng,Xue Dong,Yi-min Ding,Sunpei Hu,Runhao Zhang,Yizhou Dai,Peixin Cui,Zhou Xiao,Donghao Zhao,Liujiang Zhou,Tingting Zheng,Jianping Xiao,Jie Zeng,Chuan Xia
标识
DOI:10.1038/s41467-023-35960-z
摘要
Abstract Renewable electricity-powered CO evolution from CO 2 emissions is a promising first step in the sustainable production of commodity chemicals, but performing electrochemical CO 2 reduction economically at scale is challenging since only noble metals, for example, gold and silver, have shown high performance for CO 2 -to-CO. Cu is a potential catalyst to achieve CO 2 reduction to CO at the industrial scale, but the C-C coupling process on Cu significantly depletes CO* intermediates, thus limiting the CO evolution rate and producing many hydrocarbon and oxygenate mixtures. Herein, we tune the CO selectivity of Cu by alloying a second metal Sb into Cu, and report an antimony-copper single-atom alloy catalyst (Sb 1 Cu) of isolated Sb-Cu interfaces that catalyzes the efficient conversion of CO 2 -to-CO with a Faradaic efficiency over 95%. The partial current density reaches 452 mA cm −2 with approximately 91% CO Faradaic efficiency, and negligible C 2+ products are observed. In situ spectroscopic measurements and theoretical simulations reason that the atomic Sb-Cu interface in Cu promotes CO 2 adsorption/activation and weakens the binding strength of CO*, which ends up with enhanced CO selectivity and production rates.
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