材料科学
氨生产
氨
电化学
催化作用
硝酸盐
选择性催化还原
无机化学
还原(数学)
电极
物理化学
化学
有机化学
几何学
数学
作者
Jiaqi Ni,Jing Yan,Fuhua Li,Haifeng Qi,Qingzhu Xu,Chenliang Su,Like Sun,Hongli Sun,Jie Ding,Bin Liu
标识
DOI:10.1002/aenm.202400065
摘要
Abstract Electrochemically reducing nitrate (NO 3 − ), a common water pollutant, to valuable ammonia (NH 3 ) offers a green, sustainable, and decentralized route for ammonia synthesis. Electrochemical nitrate reduction reaction (NO 3 − RR) involves two crucial reaction steps: nitrate deoxygenation followed by nitrite hydrogenation; in particular, the nitrite hydrogenation reaction is the rate‐determining step (RDS) for NO 3 − RR. In this work, an atomically dispersed cobalt‐phosphorus (Co─P) catalytic pair (CP) with strong electronic coupling is reported. The Co site in Co─P CP effectively activates NO 3 − , while the P site in Co─P CP facilitates water dissociation to release H + , synergistically enhancing the thermodynamic and kinetic performance of electrochemical nitrate reduction to ammonia.
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