产量(工程)
氨生产
法拉第效率
氨
电化学
水溶液
无机化学
化学
亚硝酸盐
化学工程
氮气
选择性
氧化物
环境压力
等离子体
绿色化学
生物量(生态学)
催化作用
动力学
化学动力学
反应速率
反应机理
材料科学
硝酸
工作(物理)
过程(计算)
湿式氧化
大气压等离子体
作者
Zhe Meng,Jian‐Hui Yi,X. F. Sun,Haixia Zhong,Xin Deng,Dongxue Liu,Kang Xia,Miaomiao Shi,Jun‐Min Yan,Qing Jiang
出处
期刊:Small
[Wiley]
日期:2025-09-18
卷期号:21 (42): e05206-e05206
被引量:3
标识
DOI:10.1002/smll.202505206
摘要
Electricity driven nitrogen (N2) reduction (eNRR) presents one green and ambient alternative to Haber-Bosch ammonia (NH3) synthesis. However, NH3 yield rate and selectivity are extremely low due to failures in sufficient N2 activation and suppressing robust competitive reaction. Herein, efficient plasma N2 activation is matched with thermodynamically favorable electrocatalytic hydrogenation in the specially integrated system and achieves sustainable and ambient NH3 synthesis directly using air and water. Through this well-designed reactor with an optimal Cu mesh electrode, high NH3 Faradaic efficiency of 91.42% and yield rate of 14.01 mg h-1 cm-2 are achieved, largely surpassing eNRR and sole nitrite (NO2 -) electroreduction in a similar electrolyte. Using in situ experiments and theoretical calculations, it is found that NH3 synthesis mainly goes through plasma N2 oxidation into gaseous nitric oxide (NO) and aqueous NO2 -, followed by the electroreduction of these intermediates to NH3. The slightly oxidized Cu species with low coordination state and high NO affinity, which are stabilized by plasma treatment, account for the accelerated reaction kinetics of *NO hydrogenation and the suppressed combination of *H into hydrogen. This work highlights the possibility of sustainable NH3 synthesis directly from ambient air and water beyond the fossil fuel-driven synthesis process.
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