Issue 15, 2023, Issue in Progress

Electrochemical ammonia synthesis by reduction of nitrate on Au doped Cu nanowires

Abstract

Electrochemical nitrate reduction reaction (NO3RR) to synthesize valuable ammonia (NH3) is considered as a green and appealing alternative to enable an artificial nitrogen cycle. However, as there are other NO3RR pathways present, selectively guiding the reaction pathway towards NH3 is currently challenged by the lack of efficient catalyst. Here, we demonstrate a novel electrocatalyst for NO3RR consisting of Au doped Cu nanowires on a copper foam (CF) electrode (Au–Cu NWs/CF), which delivers a remarkable NH3 yield rate of 5336.0 ± 159.2 μg h−1 cm−2 and an exceptional faradaic efficiency (FE) of 84.1 ± 1.0% at −1.05 V (vs. RHE). The 15N isotopic labelling experiments confirm that the yielded NH3 is indeed from the Au–Cu NWs/CF catalyzed NO3RR process. The XPS analysis and in situ infrared spectroscopy (IR) spectroscopy characterization results indicated that the electron transfer between the Cu and Au interface and oxygen vacancy synergistically decreased the reduction reaction barrier and inhibited the generation of hydrogen in the competitive reaction, resulting in a high conversion, selectivity and FE for NO3RR. This work not only develops a powerful strategy for the rational design of robust and efficient catalysts by defect engineering, but also provides new insights for selective nitrate electroreduction to NH3.

Graphical abstract: Electrochemical ammonia synthesis by reduction of nitrate on Au doped Cu nanowires

Supplementary files

Article information

Article type
Paper
Submitted
01 Feb 2023
Accepted
17 Mar 2023
First published
28 Mar 2023
This article is Open Access
Creative Commons BY license

RSC Adv., 2023,13, 9839-9844

Electrochemical ammonia synthesis by reduction of nitrate on Au doped Cu nanowires

Y. Zha, M. Liu, J. Wang, J. Feng, D. Li, D. Zhao, S. Zhang and T. Shi, RSC Adv., 2023, 13, 9839 DOI: 10.1039/D3RA00679D

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements