电催化剂
法拉第效率
电化学
催化作用
铂金
四氢呋喃
材料科学
可逆氢电极
氨生产
无机化学
吸附
基质(水族馆)
光化学
镍
化学工程
化学
氧化还原
过渡金属
配体(生物化学)
氨
氢
分解水
电化学能量转换
氢燃料
Atom(片上系统)
电极
制氢
动力学
纳米技术
组合化学
析氧
作者
Ke Yan,Yang Hong,Zhi Wang,Depeng Wang,Tong Liu,Hua Zhong,Y. Zhang
标识
DOI:10.1002/ange.202522380
摘要
Abstract Electrocatalytic hydrogen oxidation reaction (HOR) plays crucial role in various renewable energy conversion processes. Particularly, it offers new opportunities for sustained electrochemical ammonia synthesis when coupled with lithium‐mediated nitrogen reduction. But it remains tremendous challenges due to slow reaction kinetics and rapid poisoning of catalysts in non‐aqueous electrolyte. Here, we report Ni single atom mediated Pt sites on Ni substrate (PtNi 1 /Ni) to boost efficient and durable HOR in organic electrolyte. PtNi 1 /Ni exhibits high performance of nearly 100% Faradaic efficiency (FE) and long‐term stability over 1000 h in tetrahydrofuran (THF) electrolyte, far beyond commercial Pt electrode (<0.2 h). Theoretical calculations combined with spectroscopic characterizations indicated that Ni single atom contributes to tailoring electronic structure of Pt sites via ligand effects, which effectively reduces the energy barrier of the rate‐determining step, and simultaneously as synergistic site in suppressing organic poison species through changing THF adsorption configuration and increasing energy barriers of THF oxidative decomposition. In the lithium‐mediated electrochemical ammonia synthesis electrolyzer, it also exhibits good feasibility with high ammonia FE of ∼62%. This work sheds light on the effective strategy of single atom doping for developing active and durable nonaqueous HOR electrocatalyst and presents insightful understanding of anti‐poisoning mechanism.
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