Back to Search Start Over

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

Authors :
Yin, Jie
Jin, Jing
Yin, Zhouyang
Zhu, Liu
Du, Xin
Peng, Yong
Xi, Pinxian
Yan, Chun-Hua
Sun, Shouheng
Source :
Nature Communications; 3/28/2023, Vol. 14 Issue 1, p1-10, 10p
Publication Year :
2023

Abstract

Nanostructured metal-nitrides have attracted tremendous interest as a new generation of catalysts for electroreduction of CO<subscript>2</subscript>, but these structures have limited activity and stability in the reduction condition. Herein, we report a method of fabricating FeN/Fe<subscript>3</subscript>N nanoparticles with FeN/Fe<subscript>3</subscript>N interface exposed on the NP surface for efficient electrochemical CO<subscript>2</subscript> reduction reaction (CO<subscript>2</subscript>RR). The FeN/Fe<subscript>3</subscript>N interface is populated with Fe−N<subscript>4</subscript> and Fe−N<subscript>2</subscript> coordination sites respectively that show the desired catalysis synergy to enhance the reduction of CO<subscript>2</subscript> 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<subscript>3</subscript>N synergy arises from electron transfer from Fe<subscript>3</subscript>N to FeN and the preferred CO<subscript>2</subscript> 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<subscript>2</subscript>RR. Understanding and controlling chemical environment of metal-N-catalysts is of great importance. In this work, the authors reveal FeN/Fe<subscript>3</subscript>N interface with Fe-N<subscript>4</subscript> and Fe-N<subscript>2</subscript> coordination sites for enhanced electrochemical CO<subscript>2</subscript> reduction to CO. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
20411723
Volume :
14
Issue :
1
Database :
Complementary Index
Journal :
Nature Communications
Publication Type :
Academic Journal
Accession number :
162726007
Full Text :
https://doi.org/10.1038/s41467-023-37360-9