材料科学
纳米团簇
海水
过电位
兴奋剂
催化作用
制氢
分解水
离解(化学)
电解水
氢
化学工程
电解质
无机化学
氢溢流
析氧
镍
氢燃料
电子转移
离子键合
吸附
碱性水电解
空位缺陷
纳米材料基催化剂
歧化
光化学
铂金
纳米技术
作者
Liping He,Zhengwei Cai,Chaolin Wang,Lin Yang,Wenhao Yong,Zhaoyu Jin
标识
DOI:10.1002/adfm.202514592
摘要
Abstract Hydrogen production via water electrolysis has garnered significant attention as a promising clean energy solution, but the limited availability of pure water presents a major barrier to large‐scale implementation. Efficiently utilizing seawater for the hydrogen evolution reaction (HER) remains challenging, primarily due to sluggish water dissociation kinetics and catalyst degradation in complex ionic environments. Here, Pt nanoclusters doping are integrated with phosphorus (P) vacancy engineering to modulate electron redistribution and optimize active sites. A Pt‐doped Ni 2 P catalyst with P vacancies (Pt@Ni 2 P v ) is synthesized on nickel foam, exhibiting exceptional HER activity in alkaline seawater electrolysis. Pt@Ni 2 P v achieves the industrially required current density of 1000 mA cm −2 at a low overpotential of 89 mV. Combined experimental and theoretical analyses reveal that P vacancies facilitate charge transfer to Pt nanoclusters, while Pt nanoclusters doping enhances hydrogen spillover to adjacent Ni sites. This dual modulation generates electron‐rich Pt sites that accelerate water dissociation to adsorbed hydrogen intermediates and promote hydrogen desorption, collectively boosting HER kinetics. These findings establish an effective strategy for enhancing seawater HER performance and offer new insights into the design of catalysts for scalable hydrogen energy technologies.
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