Plasma‐Assisted Synthesis of Ni‐Doped Cu‐Based Catalyst Shielded by Carbon Overlayer for Ammonia Electrosynthesis

Z Zhenhao Wang Y Yi‐Chi Wang (Beijing National Center for Electron Microscopy and Laboratory of Advanced Materials, School of Materials Science and Engineering Tsinghua University Beijing 100084 China) S Shaofeng Li (Department of Chemical Physics) Z Zhuoyong Yan (State Key Laboratory of Chemical Resource Engineering College of Chemical Engineering Beijing University of Chemical Technology Beijing 100029 P. R. China) Z Zhanhao Jiang (State Key Laboratory of Chemical Resource Engineering College of Chemical Engineering Beijing University of Chemical Technology Beijing People's Republic of China) J Jun Qi Y Yadong Du (State Key Laboratory of Chemical Resource Engineering College of Chemical Engineering Beijing University of Chemical Technology Beijing People's Republic of China) M Minggguo Zhang (State Key Laboratory of Chemical Resource Engineering College of Chemical Engineering Beijing University of Chemical Technology Beijing 100029 P. R. China) Z Zhisen Jiang (Shanghai Advanced Research Institute Chinese Academy of Sciences Shanghai 201210 P. R. China) F Fei Zhan J Jieshan Qiu (College of Chemical Engineering)

Abstract

Abstract Plasma‐enabled N 2 oxidation coupled with electrocatalytic NO x − reduction (pNOR‐eNO x − RR) represents a highly promising approach for sustainable, scalable, and distributed NH 3 production under mild conditions. However, the eNO x − RR for NH 3 synthesis is hindered by catalyst degradation, which results in low NH 3 selectivity and poor stability. Here, inspired by solid‐state source doping in photolithography, this work reports a rapid plasma shock strategy to build a Ni‐doped Cu‐based catalyst shielded by a carbon overlayer. It demonstrates long‐term stability, maintaining an NH 3 Faradaic efficiency (FE) of 96% for 156 h at a current density of 1000 mA cm −2 . More importantly, this work establishes a continuous‐flow pNOR‐eNO x − RR system using air and water as feedstocks, achieving an NH 3 yield rate of 5.36 mmol h −1 cm −2 with an NH 3 FE of 85%. In situ characterizations and theoretical calculations reveal that the carbon overlayer suppresses electrochemical surface degradation and stabilizes the coexistence of Cu 2 O and Cu during eNO 3 − RR, while Ni doping simultaneously balances the mismatch between NO 3 − adsorption and *H supply and accelerates both processes. This study provides a new approach for designing stable catalysts and offers insights into the pNOR‐eNO x − RR system, paving the way for continuous NH 3 production directly from air and water under ambient conditions.

Article Details

Volume / Issue Vol. 38, Issue 2
Published January 01, 2026
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (11)

Z

Zhenhao Wang

Y

Yi‐Chi Wang

Beijing National Center for Electron Microscopy and Laboratory of Advanced Materials, School of Materials Science and Engineering Tsinghua University Beijing 100084 China

S

Shaofeng Li

Department of Chemical Physics

Z

Zhuoyong Yan

State Key Laboratory of Chemical Resource Engineering College of Chemical Engineering Beijing University of Chemical Technology Beijing 100029 P. R. China

Z

Zhanhao Jiang

State Key Laboratory of Chemical Resource Engineering College of Chemical Engineering Beijing University of Chemical Technology Beijing People's Republic of China

J

Jun Qi

Y

Yadong Du

State Key Laboratory of Chemical Resource Engineering College of Chemical Engineering Beijing University of Chemical Technology Beijing People's Republic of China

M

Minggguo Zhang

State Key Laboratory of Chemical Resource Engineering College of Chemical Engineering Beijing University of Chemical Technology Beijing 100029 P. R. China

Z

Zhisen Jiang

Shanghai Advanced Research Institute Chinese Academy of Sciences Shanghai 201210 P. R. China

F

Fei Zhan

J

Jieshan Qiu

College of Chemical Engineering