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通过电荷转移和自旋排序的协同调控构建用于增强水氧化的磁性异质结构

Engineering Magnetic Heterostructures with Synergistic Regulation of Charge-Transfer and Spin-Ordering for Enhanced Water Oxidation.

作者信息

Hao Chongyan, Wu Yang, Zheng Xiaobo, Du Yumeng, Fan Yameng, Pang Weikong, Tadich Anton, Zhang Shujun, Frauenheim Thomas, Ma Tianyi, Li Xiaoning, Cheng Zhenxiang

机构信息

Institute for Superconducting and Electronic Materials, University of Wollongong, Wollongong, 2500, Australia.

Bremen Center for Computational Materials Science, University of Bremen, 28359, Bremen, Germany.

出版信息

Adv Sci (Weinh). 2025 Jan;12(3):e2409842. doi: 10.1002/advs.202409842. Epub 2024 Nov 26.

Abstract

The design of heterojunctions offers a crucial solution for energy conversion and storage challenges, but current research predominantly focuses on charge transfer benefits, often neglecting spin attribute regulation despite the increasing recognition of spin-sensitivity in many chemical reactions. In this study, a novel magnetic heterostructure, CoFeO@CoFeMoO, is designed to simultaneously modulate charge and spin characteristics, and systematically elucidated their synergistic impact on the oxygen evolution reaction (OER). Experimental results and density functional theory calculations confirmed that the magnetic heterostructure exhibits both charge transfer and spin polarization. It is found that the charge-transfer behavior enhances conductivity and adsorption ability through band structure regulation. Meanwhile, magnetically polarized electrons promote triplet O generation and accelerate electron transport via spin-selective pathways. Moreover, the heterostructure's effective response to external alternating magnetic fields further amplifies the spin-dependent effect and introduces a magnetothermal effect, locally heating the active sites through spin flip, thereby boosting catalytic activity. Consequently, the OER activity of the magnetic heterostructure is improved by 83.8 times at 1.5 V compared to its individual components. This magnetic heterojunction strategy presents a promising avenue for advanced catalysis through synergistic regulating of charge-transfer and spin-ordering.

摘要

异质结的设计为能量转换和存储挑战提供了关键解决方案,但目前的研究主要集中在电荷转移的益处上,尽管人们越来越认识到自旋敏感性在许多化学反应中的重要性,但往往忽视了自旋属性的调控。在本研究中,设计了一种新型磁性异质结构CoFeO@CoFeMoO,以同时调节电荷和自旋特性,并系统地阐明它们对析氧反应(OER)的协同影响。实验结果和密度泛函理论计算证实,该磁性异质结构同时表现出电荷转移和自旋极化。研究发现,电荷转移行为通过能带结构调控提高了导电性和吸附能力。同时,磁极化电子促进三重态氧的生成,并通过自旋选择性途径加速电子传输。此外,异质结构对外部交变磁场的有效响应进一步放大了自旋相关效应,并引入了磁热效应,通过自旋翻转局部加热活性位点,从而提高催化活性。因此,与单个组分相比,磁性异质结构在1.5 V时的OER活性提高了83.8倍。这种磁性异质结策略通过协同调节电荷转移和自旋有序,为先进催化提供了一条有前景的途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ecf/11744567/577bd916cf6a/ADVS-12-2409842-g002.jpg

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