Steering CO2 Electroreduction to C2+ Products via Enhancing Localized CO Coverage and Local Pressure in Conical Cavity

被引:17
作者
Li, Congcong [1 ]
Zhang, Tingting [1 ]
Liu, Heng [2 ]
Guo, Zhongyuan [2 ,3 ]
Liu, Zhongliang [1 ]
Shi, Haojun [4 ]
Cui, Jialin [1 ]
Li, Hao [2 ]
Li, Huihui [1 ]
Li, Chunzhong [1 ,4 ]
机构
[1] East China Univ Sci & Technol, Sch Chem Engn, Key Lab Ultrafine Mat, Minist Educ, Shanghai 200237, Peoples R China
[2] Tohoku Univ, Adv Inst Mat Res WPI AIMR, Sendai 9808577, Japan
[3] Zhejiang Univ, Coll Environm & Resource Sci, Hangzhou 310058, Peoples R China
[4] East China Univ Sci & Technol, Shanghai Engn Res Ctr Hierarch Nanomat, Sch Mat Sci & Engn, Shanghai 200237, Peoples R China
基金
中国国家自然科学基金;
关键词
CC coupling; *CO coverage; conical cavity structure; electrochemical CO2 reduction; local pressure; multicarbon products; ELASTIC BAND METHOD; COPPER ELECTRODES; REDUCTION; ELECTROLYSIS; MECHANISM; DESIGN;
D O I
10.1002/adma.202312204
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The electrochemical carbon dioxide (CO2) reduction reaction (CO2RR) involves a multistep proton-coupled electron transfer (PCET) process that generates a variety of intermediates, making it challenging to transform them into target products with high activity and selectivity. Here, a catalyst featuring a nanosheet-stacked sphere structure with numerous open and deep conical cavities (OD-CCs) is reported. Under the guidance of the finite-element method (FEM) simulations and theoretical analysis, it is shown that exerting control over the confinement space results in diffusion limitation of the carbon intermediates, thereby increasing local pressure and subsequently enhancing localized *CO coverage for dimerization. The nanocavities exhibit a structure-driven shift in selectivity of multicarbon (C2+) product from 41.8% to 81.7% during the CO2RR process.
引用
收藏
页数:8
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