Over 70 % Faradaic Efficiency for CO2 Electroreduction to Ethanol Enabled by Potassium Dopant-Tuned Interaction between Copper Sites and Intermediates

被引:95
作者
Ding, Lianchun [1 ]
Zhu, Nannan [1 ]
Hu, Yan [1 ]
Chen, Zheng [1 ]
Song, Pin [1 ]
Sheng, Tian [1 ]
Wu, Zhengcui [1 ]
Xiong, Yujie [1 ,2 ]
机构
[1] Anhui Normal Univ, Key Lab Funct Mol Solids, Minist Educ,Anhui Engn Res Ctr Carbon Neutral,Col, Anhui Key Lab Mol Based Mat,Anhui Prov Engn Lab N, Wuhu 241002, Peoples R China
[2] Univ Sci & Technol China, Hefei Natl Res Ctr Phys Sci Microscale, Sch Chem & Mat Sci, Hefei 230026, Peoples R China
基金
中国国家自然科学基金;
关键词
C-C Coupling; CO2; Reduction; Doping; Electrocatalysis; Ethanol; CARBON-DIOXIDE; SELECTIVE ELECTROREDUCTION; OXIDATION-STATE; REDUCTION; CU;
D O I
10.1002/anie.202209268
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
It is highly desired yet challenging to steer the CO2 electroreduction reaction (CO2ER) toward ethanol with high selectivity, for which the evolution of reaction intermediates on catalytically active sites holds the key. Herein, we report that K doping in Cu2Se nanosheets array on Cu foam serves as a versatile way to tune the interaction between Cu sites and reaction intermediates in CO2ER, enabling highly selective production of ethanol. As revealed by characterization and simulation, the electron transfer from K to Se can stabilize Cu-I species which facilitate the adsorption of linear *COL and bridge *COB intermediates to promote C-C coupling during CO2ER. As a result, the optimized K-11.2%-Cu2Se nanosheets array can catalyze CO2ER to ethanol as a single liquid product with high selectivity in a potential area from -0.6 to -1.2 V. Notably, it offers a Faradaic efficiency of 70.3 % for ethanol production at -0.8 V with as is stable for 130 h.
引用
收藏
页数:7
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