铁电性
材料科学
极化(电化学)
再分配(选举)
平面的
密度泛函理论
化学物理
金属
电子转移
凝聚态物理
纳米技术
光电子学
蚀刻(微加工)
催化作用
电子
电荷(物理)
电荷密度
氧气
工作(物理)
磁场
调制(音乐)
结晶学
自旋极化
电子结构
作者
Siying Ma,Jinyu Zhou,Ruisheng Zhang,Dongjian Jiang,Mei‐Yan Xu,Y SUN,Di Wang,Shancheng Yan,Chunlan Ma,Y H Deng,Xinglong Wu
出处
期刊:Nano Letters
[American Chemical Society]
日期:2026-07-18
卷期号:26 (29): 9622-9630
标识
DOI:10.1021/acs.nanolett.6c02454
摘要
Dynamic spin-state modulation of atomically dispersed metal sites offers a promising route to optimize catalytic reactions, yet most strategies rely on static coordination structures fixed during synthesis. Here, we report electric-field-induced spin-state reconstruction of atomically dispersed Fe sites anchored at a ferroelectric Ni(DPA)2 interface. Fe sites were introduced by controlled Fe(III)-mediated etching and stabilized through interfacial Fe-O/Fe-N coordination. Density functional theory calculations reveal that electric-field-enhanced ferroelectric polarization drives asymmetric charge redistribution at the interface, promotes electron transfer to Fe centers, and weakens the local coordination field by transforming Fe from a planar four-coordinate geometry toward an unsaturated three-coordinate configuration. Spin-projected density of states and magnetic measurements indicate that a substantial fraction of Fe(III) centers is converted into higher-spin states. Benefiting from high-spin Fe sites and improved interfacial charge transfer, Fe-Ni(DPA)2 delivers efficient oxygen evolution activity. This work establishes ferroelectric interfaces as field-responsive platforms for dynamic spin engineering.
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