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Nitrogen-Doped Porous Carbon-Supported Cu–Ni Single-Atom Catalysts for Green Ammonia Synthesis via Renewable-Powered Nitrogen Reduction Reaction.

Authors :
Yang, Miaosen
Yang, Jiayin
He, Na
Wang, Shuqi
Ni, Huiting
Yuan, Jiaxi
Kang, Yue
Liu, Yixin
Zhou, Chunxia
Tong, Liping
Lu, Binfeng
Liu, Xiyang
Wang, Quan
Huang, Senhe
Feng, Boxu
Guo, Gaijuan
Han, Sheng
Han, Zhiya
Source :
ACS Applied Nano Materials; 1/10/2025, Vol. 8 Issue 1, p179-188, 10p
Publication Year :
2025

Abstract

Ammonia (NH<subscript>3</subscript>) plays a pivotal role in industrial production and human life. The conventional method of ammonia production via the Haber–Bosch route, which operates under stringent conditions, incurs considerable energy expenditure and contributes to the release of greenhouse gases. Therefore, the development of advanced environmentally friendly methods for NH<subscript>3</subscript> synthesis is of great importance. This research endeavors to produce environmentally friendly NH<subscript>3</subscript> by harnessing the electrocatalytic nitrogen reduction reaction, powered by sustainable electricity sources, and investigate the efficacy of catalysts for this process. Non-noble-metal NiCu double single-atom-loaded nitrogen-doped porous carbon (NC@NiCu) was obtained by electrochemical deposition. Experimental results show that NC@NiCu has abundant dual single-atom Ni–Cu active sites, demonstrating excellent electrocatalytic N<subscript>2</subscript> reduction performance, with a Faradaic efficiency of 30.0% and an ammonia yield rate of 70.78 μg·h<superscript>–1</superscript>·mg<subscript>cat.</subscript><superscript>–1</superscript>, superior to many reported single-atom materials. The confirmation of uniformly dispersed Ni–Cu dual single-atom sites was achieved through the application of high-angle annular dark-field scanning transmission electron microscopy and X-ray absorption fine structure analysis. Moreover, the product of the electrochemical NRR was identified as NH<subscript>3</subscript>, which was detected using differential electrochemical mass spectrometry, and density functional theory calculations revealed that the energy barrier for the transformation from *N<subscript>2</subscript>H to *NHNH on NC@NiCu is 0.72 eV, which is 0.69 eV higher than the energy barrier from *N<subscript>2</subscript>H to *NNH<subscript>2</subscript> (0.03 eV). This significant difference in energy barriers indicates that the NRR on NC@NiCu proceeds via a distal mechanism. This research introduces an innovative method for the fabrication of nitrogen fixation materials with high catalytic activity and simultaneously establishes a fresh foundation for the development of future materials featuring dual single-atom configurations. Such advancements are pivotal for the realization of environmentally friendly and sustainable ammonia production techniques. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
25740970
Volume :
8
Issue :
1
Database :
Complementary Index
Journal :
ACS Applied Nano Materials
Publication Type :
Academic Journal
Accession number :
182215114
Full Text :
https://doi.org/10.1021/acsanm.4c05392