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单原子催化剂对水氧化的铁电极化效应

Ferroelectric Polarization Effects of Single-Atom Catalysts on Water Oxidation.

作者信息

Ma Hao, Ye Xinyu, Li Xiaoning, Xu Zhichuan J, Sun Yuanmiao

机构信息

Institute of Technology for Carbon Neutrality, Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen University Town, Shenzhen 1068 Xueyuan Avenue, Shenzhen, Guangdong, 518055, P. R. China.

Centre for Atomaterials and Nanomanufacturing (CAN), School of Science, RMIT University, Melbourne, VIC 3000, Australia.

出版信息

Adv Mater. 2025 May;37(21):e2500285. doi: 10.1002/adma.202500285. Epub 2025 Apr 7.

DOI:10.1002/adma.202500285
PMID:40190157
Abstract

The oxygen evolution reaction (OER) performance of single-atom catalysts (SACs) heavily depends on their substrates. However, heterojunctions with traditional substrate materials often fail to provide the desired dynamic interface effects. Here, through a systematic study of the ferroelectric heterostructure InSe/C-N-M, the feasibility of using ferroelectric materials to achieve dynamic optimization of the OER activity on SACs is demonstrated. The ferroelectric InSe is confirmed to be an effective substrate for improving the stability of various SACs, supported by theoretical results of their negative formation energy and positive dissolution potential. Activity analysis indicates that among these InSe/C-N-M systems, the InSe/C-N-Ir can achieve near-ideal catalytic activities through polarization switching. It can unprecedentedly catalyze OER via a hybrid pathway of adsorbate evolution mechanism and O-O coupling mechanism under different pH conditions (from pH = 1 to pH = 13). Machine learning models have been developed to conduct feature analysis and make ultrafast predictions of OER activity, which identify that the interfacial charge transfer triggered by ferroelectric polarization is the key to fine-tuning the OER performance of SACs. This work provides a theoretical framework that utilizes ferroelectric polarization as a powerful approach to navigate the design of efficient SACs.

摘要

单原子催化剂(SACs)的析氧反应(OER)性能在很大程度上取决于其基底。然而,与传统基底材料形成的异质结往往无法提供所需的动态界面效应。在此,通过对铁电异质结构InSe/C-N-M进行系统研究,证明了使用铁电材料实现对SACs上OER活性进行动态优化的可行性。铁电体InSe被证实是提高各种SACs稳定性的有效基底,其负形成能和正溶解电位的理论结果支持了这一点。活性分析表明,在这些InSe/C-N-M体系中,InSe/C-N-Ir可通过极化切换实现近乎理想的催化活性。它能够在不同pH条件下(从pH = 1到pH = 13)以前所未有的方式通过吸附质演化机制和O-O偶联机制的混合途径催化OER。已开发机器学习模型进行特征分析并对OER活性进行超快预测,该模型确定由铁电极化触发的界面电荷转移是微调SACs的OER性能的关键。这项工作提供了一个理论框架,利用铁电极化作为一种强大的方法来指导高效SACs的设计。

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引用本文的文献

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