氢氧化物
电解
析氧
碱性水电解
催化作用
电解水
材料科学
电子结构
分解水
化学工程
化学
氧气
数码产品
纳米技术
平方(代数)
活动站点
质子
无机化学
密度泛函理论
电压
化学物理
作者
Xinyi Li,Jiayi Liu,Zheng Wang,Hong Hsin Huang,X.B. Sun,Wenting Lu,Xiao Dan Zhao
出处
期刊:Science Advances
[American Association for the Advancement of Science]
日期:2026-02-25
卷期号:12 (9): eaea8247-eaea8247
被引量:15
标识
DOI:10.1126/sciadv.aea8247
摘要
Coordination engineering is often used to tune the electronic structures of active sites, while their catalytic performances are determined not only by electronic structures but also by microenvironments. Herein, we introduce interfacial functional ligands that not only optimize the electronic structures of active sites but also regulate the interfacial microenvironment for oxygen evolution reaction (OER). Specifically, the pore edge–hosted FeF 3 O 2 sites enable a favorable electronic structure to generate * OOH intermediates and simultaneously promote the interfacial transport of hydroxide for enhanced OER kinetics. The F ligands in FeF 3 O 2 sites interact with interfacial water strongly via H-bonding to promote H-bond network connectivity, thus encouraging the temporally concerted proton transfer during hydroxide diffusion. Consequently, FeF 3 O 2 sites realize the 331.5-fold enhancement in turnover frequency for alkaline OER over the NiOOH and efficient water electrolyzers (1.663 voltage at 1.0 amperes per square centimeter at 60°C, durably operating at 1.0 amperes per square centimeter > 1200 hours).
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