选择性
催化作用
电化学
乙烯
化学
串联
乙醇
无机化学
碳纤维
材料科学
化学工程
电极
有机化学
物理化学
复合材料
工程类
复合数
作者
Jie Zhang,Thi Ha My Pham,Youngdon Ko,Mo Li,Shuliang Yang,Cedric David Koolen,Liping Zhong,Wen Luo,Andreas Züttel
标识
DOI:10.1016/j.xcrp.2022.100949
摘要
CO-selective metals (e.g., Ag) on Cu catalysts improve the selectivity of multi-carbon (C2+) products in electrochemical CO2 reduction. However, the origin of the improvement remains unclear due to the convolution of tandem and interface effects. Here, Ag@C@Cu core-shell catalysts were synthesized, in which the thin carbon interlayer inhibited the direct interaction between Ag and Cu while still allowing the reduction of CO2 on Ag, thus isolating the tandem effect from other effects. This catalyst produced higher ratios of ethanol to ethylene relative to the monometallic Cu catalyst, demonstrating that the locally increased CO concentration promoted the ethanol pathway over the ethylene pathway. Further, the selectivity of ethanol was optimized by tuning the thickness of the Cu shell. This work provides a rational approach to design core-shell catalysts for understanding structure-performance relationships and demonstrates the key role of the tandem effect in tuning the selectivity of C2+ products.
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