Rapid Fabrication of N-, Cu-, and Co-Doped Electrodes with Strong Electronic Coupling by Cold Plasma for Electrocatalytic Reduction of Nitrate to Ammonia

被引:0
|
作者
Xiang, Hongyu [1 ,2 ]
Yue, Xufeng [3 ]
Chu, Yinghao [2 ]
Shu, Song [1 ]
机构
[1] Sichuan Univ, Coll Carbon Neutral Future Technol, Chengdu 610065, Sichuan, Peoples R China
[2] Sichuan Univ, Coll Architecture & Environm, Chengdu 610065, Sichuan, Peoples R China
[3] Sichuan Univ, Sch Mech Engn, Chengdu 610065, Sichuan, Peoples R China
基金
中国国家自然科学基金;
关键词
PERFORMANCE; CATALYSTS; GRAPHENE;
D O I
10.1021/acs.inorgchem.4c03089
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Electrochemical NOx- reduction (NOxRR) is a sustainable technology for ammonia synthesis. The development of a simple, fast, and economical catalytic electrode preparation technique is crucial for large-scale ammonia synthesis. Herein, we propose a plate-to-plate DBD plasma strategy to synthesize the catalytic electrodes M-N/CP (M = Cu, Co, Ni, CuCo, and CuNi), achieving in suit codoping of N and bimetals on carbon paper (CP) at room temperature within 3 h. N-doping improves the metal loading and the NOxRR performance by forming N-M bonds. The electronic coupling and synergistic effect of Cu and Co sites facilitate the relay conversion of NO3- to NO2- to NH3. Notably, the NO3- removal efficiency of CuCo-N/CP reaches 82%, with NH3 yield rate of 346 mu g h(-1) cm(-2), and the faradaic efficiency is as high as 86% at -0.58 V vs RHE, which remains competitive in terms of NOxRR performance. Importantly, wet flue gas denitrification and desulfurization coupled with electrocatalytic reduction can convert NOx and SO2 to (NH4)(2)SO4, Additionally, the maneuverability of plasma technology offers the potential for batch preparation of CuCo-N/CP electrodes for electrochemically driven wet denitrification wastewater valorization.
引用
收藏
页码:19809 / 19818
页数:10
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