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FeS2@TiO2 nanobelt array enabled high-efficiency electrocatalytic nitrate reduction to ammonia.

Authors :
Wang, Haipeng
Zhao, Donglin
Liu, Chaozhen
Fan, Xiaoya
Li, Zerong
Luo, Yongsong
Zheng, Dongdong
Sun, Shengjun
Chen, Jie
Zhang, Jing
Liu, Yang
Gao, Shuyan
Gong, Feng
Sun, Xuping
Source :
Journal of Materials Chemistry A; 12/14/2022, Vol. 10 Issue 46, p24462-24467, 6p
Publication Year :
2022

Abstract

Nitrate (NO<subscript>3</subscript><superscript>−</superscript>), which exists in both surface water and underground water, is harmful to the environment and human body. Ammonia (NH<subscript>3</subscript>) is a kind of necessary produced chemical for industry and daily life. Electrochemical NO<subscript>3</subscript><superscript>−</superscript> reduction can eliminate hazardous NO<subscript>3</subscript><superscript>−</superscript> and produce value-added NH<subscript>3</subscript> at the same time under ambient conditions but requires efficient catalysts for the NO<subscript>3</subscript><superscript>−</superscript> reduction reaction (NO<subscript>3</subscript>RR) with high selectivity. Herein, we report on the development of FeS<subscript>2</subscript> nanoparticles on TiO<subscript>2</subscript> nanobelt array (FeS<subscript>2</subscript>@TiO<subscript>2</subscript>) as an earth-abundant NO<subscript>3</subscript>RR electrocatalyst. It shows superior electrocatalytic performance with a large NH<subscript>3</subscript> yield of 860.3 μmol h<superscript>−1</superscript> cm<superscript>−2</superscript> at −0.7 V and a high faradaic efficiency of 97.0% at −0.4 V versus reversible hydrogen electrode in 0.1 M NaOH with 0.1 M NO<subscript>3</subscript><superscript>−</superscript>. The theoretical calculations reveal the mechanisms of the enhanced NO<subscript>3</subscript>RR performance of FeS<subscript>2</subscript>@TiO<subscript>2</subscript>. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
20507488
Volume :
10
Issue :
46
Database :
Complementary Index
Journal :
Journal of Materials Chemistry A
Publication Type :
Academic Journal
Accession number :
160486664
Full Text :
https://doi.org/10.1039/d2ta07475c