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Boosting ammonia production in electrocatalytic NOx reduction on a robust Fe/FeMoO4 catalyst.

Authors :
Liu, Dong-Xue
Deng, Xin
Zhu, Yong-Fu
Meng, Zhe
Sun, Xue-Feng
Shi, Miao-Miao
Zhong, Hai-Xia
Yan, Jun-Min
Source :
Nano Research; Jul2024, Vol. 17 Issue 7, p5801-5806, 6p
Publication Year :
2024

Abstract

Electrocatalytic reduction of nitrate (NO 3 −) and nitride (NO 2 −) to ammonia (NH<subscript>3</subscript>) is of wide interest as a promising alternative to the energy-intensive Haber-Bosch route for mitigating the vast energy consumption and the accompanied carbon dioxide emission, as well as benefiting for the relevant sewage treatment. However, exploring an efficient and low-cost catalyst with high atomic utilization that can effectively facilitate the slow multi-electron transfer process remains a grand challenge. Herein, we present an efficient hydrogenation of NO 3 − / NO 2 − species to NH<subscript>3</subscript> in both alkaline and neutral environments over the Fe<subscript>2</subscript>(MoO<subscript>4</subscript>)<subscript>3</subscript> derived hybrid electrocatalyst with the metallic Fe site on FeMoO<subscript>4</subscript> (Fe/FeMoO<subscript>4</subscript>). The Mo ingredient can play a synergistically positive role in further promoting the NH<subscript>3</subscript> production on Fe. As a result, Fe/FeMoO<subscript>4</subscript> behaves well in the electrochemical NH<subscript>3</subscript> generation from NO 2 − with a maximum NH<subscript>3</subscript> Faradaic efficiency (FE) of 96.53% and 87.68% in alkaline and neutral electrolyte, corresponding to the NH<subscript>3</subscript> yield rate of 640.68 and 302.56 mg ⋅ h − 1 ⋅ mg cat. − 1 , respectively, which outperforms the Fe and Mo counterpart and other similar catalyst, showing the robust catalytic capacity of each active site. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
19980124
Volume :
17
Issue :
7
Database :
Complementary Index
Journal :
Nano Research
Publication Type :
Academic Journal
Accession number :
178276954
Full Text :
https://doi.org/10.1007/s12274-024-6661-y