材料科学
催化作用
法拉第效率
氨
可逆氢电极
氨生产
氢
吸附
硝酸盐
无机化学
化学工程
电极
光化学
金属有机骨架
产量(工程)
电化学
制氢
分解水
纳米技术
金属
双金属片
氢燃料
电催化剂
Atom(片上系统)
标准氢电极
工作(物理)
人工光合作用
碳纤维
选择性催化还原
作者
Zhuyu Luo,Linfeng He,Linwei Han,Xiaoyan Liu,Shan Hu,Liangyu Qiang,Nuo Chen,Hexing Li,Dieqing Zhang
标识
DOI:10.1002/adfm.202527094
摘要
ABSTRACT The photo assisted electrocatalytic nitrate reduction reaction (PEC‐NO 3 RR) for ammonia synthesis presents a green pathway for ammonia production from nitrate pollutants. Curved coordination environments in metal single atoms (SAs) based catalysts offer unique opportunities for tuning local electronic structures and thus improve their catalytic activity, yet has not been explored in PEC‐NO 3 RR. In this work, curvature‐engineered Co SAs active sites supported on HOFs matrix (CDs@Co SAs ‐HOFs) is designed. The atomically dispersed Co sites naturally adopt a curved Co‐N/O configuration. Compared to planar Co SAs sites, this curved Co SAs have higher d ‐band center, facilitating the adsorption towards NO 3 − and relative intermediates during NO 3 RR. Moreover, the energy barriers for * NO hydrogenation, which is considered as the rate‐determining step, has been significantly reduced on the curved Co SAs sites. With the incorporated carbon dots as light harvesting units, CDs@Co SAs ‐HOFs delivers a high ammonia yield of 135.12 µmol h −1 cm −2 and Faradaic efficiency of 92.01% at −0.4 V versus reversible hydrogen electrode (vs. RHE) under light irradiation. This work demonstrates a route for optimizing and boosting photo assisted electrocatalytic activity of the single atom catalysts by regulating the local geometric configurations, which may be applied in other catalytic reactions.
科研通智能强力驱动
Strongly Powered by AbleSci AI