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The built-in electric field across FeN/Fe3N interface for efficient electrochemical reduction of CO2 to CO
The built-in electric field across FeN/Fe3N interface for efficient electrochemical reduction of CO2 to CO
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The built-in electric field across FeN/Fe3N interface for efficient electrochemical reduction of CO2 to CO
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The built-in electric field across FeN/Fe3N interface for efficient electrochemical reduction of CO2 to CO
The built-in electric field across FeN/Fe3N interface for efficient electrochemical reduction of CO2 to CO

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The built-in electric field across FeN/Fe3N interface for efficient electrochemical reduction of CO2 to CO
The built-in electric field across FeN/Fe3N interface for efficient electrochemical reduction of CO2 to CO
Journal Article

The built-in electric field across FeN/Fe3N interface for efficient electrochemical reduction of CO2 to CO

2023
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Overview
Nanostructured metal-nitrides have attracted tremendous interest as a new generation of catalysts for electroreduction of CO 2 , but these structures have limited activity and stability in the reduction condition. Herein, we report a method of fabricating FeN/Fe 3 N nanoparticles with FeN/Fe 3 N interface exposed on the NP surface for efficient electrochemical CO 2 reduction reaction (CO 2 RR). The FeN/Fe 3 N interface is populated with Fe−N 4 and Fe−N 2 coordination sites respectively that show the desired catalysis synergy to enhance the reduction of CO 2 to CO. The CO Faraday efficiency reaches 98% at −0.4 V vs. reversible hydrogen electrode, and the FE stays stable from −0.4 to −0.9 V during the 100 h electrolysis time period. This FeN/Fe 3 N synergy arises from electron transfer from Fe 3 N to FeN and the preferred CO 2 adsorption and reduction to *COOH on FeN. Our study demonstrates a reliable interface control strategy to improve catalytic efficiency of the Fe–N structure for CO 2 RR. Understanding and controlling chemical environment of metal-N-catalysts is of great importance. In this work, the authors reveal FeN/Fe 3 N interface with Fe-N 4 and Fe-N 2 coordination sites for enhanced electrochemical CO 2 reduction to CO.