催化作用
化学
氨
无机化学
电催化剂
还原(数学)
氮气
氮氧化物
氨生产
电化学
氧还原反应
选择性催化还原
氧化还原
氧还原
电极
作者
Chenxi Man,Bingtao Xie,Lun Li,X X Xu,Shuai Zhang,Bangdou Huang,Liguang Dou,Dengke Xi,Xuekai Pei,Leslie Petrik,Cheng Zhang,Tao Shao
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2026-04-16
被引量:1
标识
DOI:10.1021/acscatal.6c01004
摘要
The electrocatalytic reduction of nitrogen oxides (NO x ) to ammonia represents a promising alternative to direct N 2 reduction but is often limited by low reaction rates, poor selectivity, and severe competition from hydrogen evolution under dilute feed conditions. Here, we report a plasma-enabled electrocatalytic strategy for efficient NO x -to-NH 3 conversion using an electronically engineered Cu-N-P catalyst. A rotating gliding arc plasma converts air into reactive NO x species, providing a continuous and controllable feed for downstream electrochemical reduction. The Cu-N-P catalyst achieves an ammonia production rate of 2.36 mmol h −1 cm −2 with nearly 100% Faradaic efficiency at −0.575 V versus RHE and maintains stable operation for over 125 h under plasma-derived NO x conditions. Compared with unmodified Cu, the N, P co-doped catalyst promotes selective NO x adsorption and accelerates the hydrogenation of key intermediates while suppressing parasitic hydrogen evolution. Spectroscopic characterizations and theoretical analysis reveal that electronic structure modulation facilitates efficient NO x utilization and favorable hydrogenation kinetics. This work establishes an effective catalytic pathway for NO x -to-ammonia conversion under plasma-assisted conditions, providing insights into catalyst design for coupled plasma-electrochemical nitrogen conversion systems.
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