材料科学
选择性
纳米片
格式化
极限抗拉强度
电化学
化学工程
吸附
纳米材料
可逆氢电极
纳米技术
无机化学
电极
催化作用
冶金
物理化学
工作电极
有机化学
工程类
化学
作者
Yingzheng Zhang,Haeseong Jang,Xin Ge,Wei Zhang,Zijian Li,Liqiang Hou,Li Zhai,Xiaoqian Wei,Zhe Wang,Min Gyu Kim,Shangguo Liu,Qing Qin,Xien Liu,Jaephil Cho
标识
DOI:10.1002/aenm.202202695
摘要
Abstract In general, commercial ZnO owns the poor selectivity and activity toward electroreduction CO 2 to formate. In contrast, the numbers of Sn‐based nanomaterials are reported as excellent electrocatalysts for formate production, however, the metallic Sn is more expensive than Zn. In this study, it is demonstrated that an atomically dispersed Sn on a tensile‐strained ZnO nanosheet (Sn SA/ZnO) shows dramatically improved activity and selectivity for formate production over a wide potential window compared with that of commercial ZnO. Especially, Sn SA/ZnO exhibits 205‐fold mass activity enhancement than the commercial Sn at −1.7 V versus reversible hydrogen electrode normalized with element Sn. The experimental measurements combined with theoretical calculations revealed that Sn SA/ZnO can effectively capture and activate CO 2 by its exposed double‐active sites (Sn and O), while the tensile strain on its surface boosts the catalytic selectivity by strengthening the adsorption of the *HCOO intermediate for the electrochemical reduction of CO 2 to formate.
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