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- W4226129251 abstract "Abstract Carbon‐supported nitrogen‐coordinated single‐metal site catalysts (i.e., M−N−C, M: Fe, Co, or Ni) are active for the electrochemical CO 2 reduction reaction (CO 2 RR) to CO. Further improving their intrinsic activity and selectivity by tuning their N−M bond structures and coordination is limited. Herein, we expand the coordination environments of M−N−C catalysts by designing dual‐metal active sites. The Ni‐Fe catalyst exhibited the most efficient CO2RR activity and promising stability compared to other combinations. Advanced structural characterization and theoretical prediction suggest that the most active N‐coordinated dual‐metal site configurations are 2N‐bridged (Fe‐Ni)N 6 , in which FeN 4 and NiN 4 moieties are shared with two N atoms. Two metals (i.e., Fe and Ni) in the dual‐metal site likely generate a synergy to enable more optimal *COOH adsorption and *CO desorption than single‐metal sites (FeN 4 or NiN 4 ) with improved intrinsic catalytic activity and selectivity." @default.
- W4226129251 created "2022-05-05" @default.
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- W4226129251 date "2022-05-09" @default.
- W4226129251 modified "2023-10-14" @default.
- W4226129251 title "Atomically Dispersed Dual‐Metal Site Catalysts for Enhanced CO<sub>2</sub> Reduction: Mechanistic Insight into Active Site Structures" @default.
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- W4226129251 doi "https://doi.org/10.1002/ange.202205632" @default.
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