Low‐Voltage Driven Co‐Production of Ammonia, Formate, and Hydrogen From Nitrite Reduction Coupled Formaldehyde Oxidation System on Ultra‐Stable AuCuRh Nanowires under Illumination

Z Ze‐Nong Zhang (Key Laboratory of Macromolecular Science of Shaanxi Province School of Chemistry and Chemical Engineering Shaanxi Normal University Xi'an 710062 P. R. China) X Xiao‐Hui Wang (Key Laboratory of Macromolecular Science of Shaanxi Province School of Chemistry and Chemical Engineering Shaanxi Normal University Xi'an 710062 P. R. China) W Wei Zhong X Xuan Ai (Key Laboratory of Applied Surface and Colloid Chemistry (Ministry of Education) Key Laboratory of Macromolecular Science of Shaanxi Province Shaanxi Key Laboratory for Advanced Energy Devices School of Materials Science and Engineering Shaanxi Normal University Xi'an China) X Xin Wang S Shu‐Ni Li (Key Laboratory of Macromolecular Science of Shaanxi Province School of Chemistry and Chemical Engineering Shaanxi Normal University Xi'an 710062 P. R. China) B Bao Yu Xia (State Key Laboratory of New Textile Materials and Advanced Processing, Key Laboratory of Material Chemistry for Energy Conversion and Storage (Ministry of Education), Hubei Key Laboratory of Material Chemistry and Service Failure, School of Chemistry and Chemical Engineering) Y Yu Chen

Abstract

Abstract The nitrite electroreduction reaction (NO 2 RR) offers a green and sustainable pathway for environmental wastewater treatment and ammonia (NH 3 ) generation. Herein, defect‐rich trimetallic AuCuRh nanowires (AuCuRh NWs) with a large number of grain boundaries, twin boundaries, and atomic steps are successfully synthesized by galvanic replacement reaction. Due to its self‐stability and high activity, AuCuRh NWs can efficiently drive the stable NO 2 RR at 0 V potential (Faradaic efficiency: 98.32%, NH 3 yield rate: 20.49 mg h −1 mg cat −1 ). Moreover, AuCuRh NWs also reveal excellent electrocatalytic activity for the formaldehyde electrooxidation reaction (FOR), which can reach 10 mA cm −2 at only 0.35 V potential. The NO 2 RR||FOR electrolysis system assembled with AuCuRh NWs requires only the electrolysis voltage of 0.38 V to achieve the co‐production of NH 3 , formate, and hydrogen and ultra‐stable continuous electrolysis for 300 hours. The NO 2 RR||FOR electrolysis system can be further decreased to only 0.29 V under illumination due to plasmon‐enhanced activity. This study provides an energy‐efficient coupling strategy for the stable co‐production of value‐added chemicals.

Article Details

Volume / Issue Vol. 38, Issue 4
Published January 01, 2026
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (8)

Z

Ze‐Nong Zhang

Key Laboratory of Macromolecular Science of Shaanxi Province School of Chemistry and Chemical Engineering Shaanxi Normal University Xi'an 710062 P. R. China

X

Xiao‐Hui Wang

Key Laboratory of Macromolecular Science of Shaanxi Province School of Chemistry and Chemical Engineering Shaanxi Normal University Xi'an 710062 P. R. China

W

Wei Zhong

X

Xuan Ai

Key Laboratory of Applied Surface and Colloid Chemistry (Ministry of Education) Key Laboratory of Macromolecular Science of Shaanxi Province Shaanxi Key Laboratory for Advanced Energy Devices School of Materials Science and Engineering Shaanxi Normal University Xi'an China

X

Xin Wang

S

Shu‐Ni Li

Key Laboratory of Macromolecular Science of Shaanxi Province School of Chemistry and Chemical Engineering Shaanxi Normal University Xi'an 710062 P. R. China

B

Bao Yu Xia

State Key Laboratory of New Textile Materials and Advanced Processing, Key Laboratory of Material Chemistry for Energy Conversion and Storage (Ministry of Education), Hubei Key Laboratory of Material Chemistry and Service Failure, School of Chemistry and Chemical Engineering

Y

Yu Chen