磷化物
材料科学
电解
无定形固体
比例(比率)
碱性水电解
异质结
纳米技术
工程物理
光电子学
冶金
结晶学
电极
物理化学
化学
工程类
物理
镍
电解质
量子力学
作者
Xin Wang,Ziyu Zhang,Huaizheng Zhang,S.Q. Lin,Chen Li,Yifan Xie,Yunlong Zhang,Feng Shi,Dong Liu,Zhen‐Bo Wang
标识
DOI:10.1002/adfm.202514137
摘要
Abstract Alkaline water electrolysis is a promising pathway for large‐scale hydrogen production, yet its efficiency is limited by the sluggish kinetics of the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER). Herein, a bifunctional CoFeP electrocatalyst is reported featuring a crystalline/amorphous heterostructure with engineered built‐in electric fields (BEFs). The integration of crystalline CoP and Fe 2 P domains with amorphous regions induces interfacial charge redistribution, driven by work function differences, which in turn generates BEFs that modulate the electronic structure and optimize the d‐band center. This tuning enhances the adsorption/desorption energetics of reaction intermediates, thereby boosting catalytic performance. As a result, CoFeP delivers low overpotentials of 199 mV for HER and 329 mV for OER at 1 A cm −2 in 1 m KOH. Remarkably, the catalyst exhibits outstanding durability over 1500 h under industrially relevant conditions (6 m KOH, 80 °C, 0.5 A cm −2 ). Technoeconomic analysis estimates a hydrogen production cost of $1.10 per gasoline gallon equivalent, significantly below the U.S. DOE's 2026 target. A rational design strategy is offered here for interface and electronic structure engineering and a viable platform is presented for next‐generation industrial water electrolysis.
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