Modulating the local coordination structure of metal single-atom catalysts(SACs)is extensively employed to tune the catalytic activity,but rarely involved in regulating the reaction pathway which fundamentally determi...Modulating the local coordination structure of metal single-atom catalysts(SACs)is extensively employed to tune the catalytic activity,but rarely involved in regulating the reaction pathway which fundamentally determines the product selectivity.Herein,we report that the product selectivity of electrochemical CO_(2)reduction(CO_(2)RR)on the single-atom indium-NxC4-x(1≤x≤4)catalysts could be tuned from formate to CO by varying the carbon and nitrogen occupations in the first coordination sphere.Surprisingly,the optimal In SAC showed great promise for CO production with the maximum Faradic efficiency of 97%,greatly different from the reported In-based catalysts where the formate is the dominant product.Combined experimental verifications and theoretical simulations reveal that the selectivity switch from formate to CO on In SACs originates from active sites shift from indium center to the indium-adjacent carbon atom,where the indium site favors formate formation and the indium-adjacent carbon site prefers the CO pathway.The present work suggests the active sites in metal SACs may shift from the widely accepted metal center to surrounding carbon atoms,thereby offering a new implication to revisit the active sites for metal SACs.展开更多
基金supported by the National Natural Science Foundation of China (22322902,U22A20396,22102052,22309050,and 22211540385)the National Key Research and Development Program of China (2021YFA1502000)+3 种基金the Science and Technology Innovation Program of Hunan Province (2021RC3065)Jiebang Guashuai Project of Changsha City (kq2301009)Shenzhen Science and Technology Program (JCYJ20210324120800002,JCYJ20220818100012025,and JCYJ20230807122007015)China Postdoctoral Science Foundation (2023T160205)。
基金This work was supported by the National Natural Science Foundation of China(Nos.21905089,2021RC3065,and 2021RC2053)the National Key Research and Development Program of China(No.2021YFA1502000)+3 种基金the Science and Technology Innovation Program of Hunan Province(Nos.2021RC3065 and 2021RC2053)Hunan Provincial Natural Science Foundation of China(No.2020JJ2001)Shenzhen Science and Technology Program(No.JCYJ20210324120800002)the Hefei National Laboratory for Physical Sciences at the Microscale(No.KF2020108).
文摘Modulating the local coordination structure of metal single-atom catalysts(SACs)is extensively employed to tune the catalytic activity,but rarely involved in regulating the reaction pathway which fundamentally determines the product selectivity.Herein,we report that the product selectivity of electrochemical CO_(2)reduction(CO_(2)RR)on the single-atom indium-NxC4-x(1≤x≤4)catalysts could be tuned from formate to CO by varying the carbon and nitrogen occupations in the first coordination sphere.Surprisingly,the optimal In SAC showed great promise for CO production with the maximum Faradic efficiency of 97%,greatly different from the reported In-based catalysts where the formate is the dominant product.Combined experimental verifications and theoretical simulations reveal that the selectivity switch from formate to CO on In SACs originates from active sites shift from indium center to the indium-adjacent carbon atom,where the indium site favors formate formation and the indium-adjacent carbon site prefers the CO pathway.The present work suggests the active sites in metal SACs may shift from the widely accepted metal center to surrounding carbon atoms,thereby offering a new implication to revisit the active sites for metal SACs.
