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用于高效析氧反应的活化表面重构的最新进展。

Recent advances in activating surface reconstruction for the high-efficiency oxygen evolution reaction.

作者信息

Gao Likun, Cui Xun, Sewell Christopher D, Li Jian, Lin Zhiqun

机构信息

School of Materials Science and Engineering, Georgia Institute of Technology, Atlanta, GA 30332, USA.

出版信息

Chem Soc Rev. 2021 Aug 7;50(15):8428-8469. doi: 10.1039/d0cs00962h. Epub 2021 Jul 14.

Abstract

A climax in the development of cost-effective and high-efficiency transition metal-based electrocatalysts has been witnessed recently for sustainable energy and related conversion technologies. In this regard, structure-activity relationships based on several descriptors have already been proposed to rationally design electrocatalysts. However, the dynamic reconstruction of the surface structures and compositions of catalysts during electrocatalytic water oxidation, especially during the anodic oxygen evolution reaction (OER), complicate the streamlined prediction of the catalytic activity. With the achievements in operando and in situ techniques, it has been found that electrocatalysts undergo surface reconstruction to form the actual active species in situ accompanied with an increase in their oxidation state during OER in alkaline solution. Accordingly, a thorough understanding of the surface reconstruction process plays a critical role in establishing unambiguous structure-composition-property relationships in pursuit of high-efficiency electrocatalysts. However, several issues still need to be explored before high electrocatalytic activities can be realized, as follows: (1) the identification of initiators and pathways for surface reconstruction, (2) establishing the relationships between structure, composition, and electrocatalytic activity, and (3) the rational manipulation of in situ catalyst surface reconstruction. In this review, the recent progress in the surface reconstruction of transition metal-based OER catalysts including oxides, non-oxides, hydroxides and alloys is summarized, emphasizing the fundamental understanding of reconstruction behavior from the original precatalysts to the actual catalysts based on operando analysis and theoretical calculations. The state-of-the-art strategies to tailor the surface reconstruction such as substituting/doping with metals, introducing anions, incorporating oxygen vacancies, tuning morphologies and exploiting plasmonic/thermal/photothermal effects are then introduced. Notably, comprehensive operando/in situ characterization together with computational calculations are responsible for unveiling the improvement mechanism for OER. By delivering the progress, strategies, insights, techniques, and perspectives, this review will provide a comprehensive understanding of the surface reconstruction in transition metal-based OER catalysts and future guidelines for their rational development.

摘要

最近,在可持续能源及相关转换技术领域,具有成本效益和高效的过渡金属基电催化剂的发展达到了一个高潮。在这方面,基于若干描述符的结构-活性关系已经被提出,以合理设计电催化剂。然而,在电催化水氧化过程中,尤其是在阳极析氧反应(OER)期间,催化剂表面结构和组成的动态重构使催化活性的简化预测变得复杂。随着原位和实时监测技术的发展,人们发现电催化剂在碱性溶液中进行OER时会发生表面重构,原位形成实际的活性物种,同时其氧化态增加。因此,深入了解表面重构过程对于建立明确的结构-组成-性能关系以追求高效电催化剂起着关键作用。然而,在实现高电催化活性之前,仍有几个问题需要探索,如下:(1)表面重构引发剂和途径的识别;(2)建立结构、组成和电催化活性之间的关系;(3)原位催化剂表面重构的合理调控。在这篇综述中,总结了过渡金属基OER催化剂(包括氧化物、非氧化物、氢氧化物和合金)表面重构的最新进展,强调基于原位分析和理论计算,从原始预催化剂到实际催化剂对重构行为的基本理解。随后介绍了调整表面重构的最新策略,如金属替代/掺杂、引入阴离子、引入氧空位、调整形貌以及利用等离子体/热/光热效应。值得注意的是,全面的原位/实时监测表征以及计算计算有助于揭示OER的改进机制。通过阐述进展、策略、见解、技术和观点,本综述将提供对过渡金属基OER催化剂表面重构的全面理解以及其合理开发的未来指导方针。

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