Xin Wang, Ziyu Zhang, Huaizheng Zhang, Si Lin, Chen Li, Yifan Xie, Yunlong Zhang, Shi Feng, Dong Liu, Zhenbo Wang
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引用次数: 0
摘要
碱水电解是一种很有前途的大规模制氢途径,但其效率受到析氢反应(HER)和析氧反应(OER)缓慢动力学的限制。本文报道了一种双功能CoFeP电催化剂,具有晶体/非晶异质结构和工程内建电场(bef)。晶体CoP和Fe2P域与非晶态区域的集成引起了界面电荷的重新分配,这是由功函数差异驱动的,从而产生了调制电子结构和优化d波段中心的bef。这种调整提高了反应中间体的吸附/解吸能量,从而提高了催化性能。因此,在1a cm−2、1m KOH条件下,CoFeP的HER过电位为199 mV, OER过电位为329 mV。值得注意的是,该催化剂在工业相关条件下(6 m KOH, 80°C, 0.5 A cm−2)具有超过1500小时的优异耐久性。技术经济分析估计,氢气生产成本为每加仑汽油1.10美元,远低于美国能源部2026年的目标。为界面和电子结构工程提供了合理的设计策略,并为下一代工业水电解提供了可行的平台。
Crystalline/Amorphous Phosphide Heterostructures with Built‐in Electric Fields for Efficient and Long‐Term Industrial‐Scale Alkaline Water Electrolysis
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 Fe2P 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.
期刊介绍:
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