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用于高效析氧电催化的高价氧化物

High-Valence Oxides for High Performance Oxygen Evolution Electrocatalysis.

作者信息

Wang Hao, Zhai Tingting, Wu Yifan, Zhou Tao, Zhou Binbin, Shang Congxiao, Guo Zhengxiao

机构信息

Department of Chemistry, The University of Hong Kong, Hong Kong SAR, 000000, China.

Green Catalysis Center, College of Chemistry, Zhengzhou University, Zhengzhou, 450001, China.

出版信息

Adv Sci (Weinh). 2023 Aug;10(22):e2301706. doi: 10.1002/advs.202301706. Epub 2023 May 30.

Abstract

Valence tuning of transition metal oxides is an effective approach to design high-performance catalysts, particularly for the oxygen evolution reaction (OER) that underpins solar/electric water splitting and metal-air batteries. Recently, high-valence oxides (HVOs) are reported to show superior OER performance, in association with the fundamental dynamics of charge transfer and the evolution of the intermediates. Particularly considered are the adsorbate evolution mechanism (AEM) and the lattice oxygen-mediated mechanism (LOM). High-valence states enhance the OER performance mainly by optimizing the e -orbital filling, promoting the charge transfer between the metal d band and oxygen p band. Moreover, HVOs usually show an elevated O 2p band, which triggers the lattice oxygen as the redox center and enacts the efficient LOM pathway to break the "scaling" limitation of AEM. In addition, oxygen vacancies, induced by the overall charge-neutrality, also promote the direct oxygen coupling in LOM. However, the synthesis of HVOs suffers from relatively large thermodynamic barrier, which makes their preparation difficult. Hence, the synthesis strategies of the HVOs are discussed to guide further design of the HVO electrocatalysts. Finally, further challenges and perspectives are outlined for potential applications in energy conversion and storage.

摘要

过渡金属氧化物的价态调控是设计高性能催化剂的有效方法,尤其适用于支撑太阳能/电分解水及金属空气电池的析氧反应(OER)。最近,据报道高价氧化物(HVO)表现出优异的OER性能,这与电荷转移的基本动力学及中间体的演变有关。特别值得考虑的是吸附质演变机制(AEM)和晶格氧介导机制(LOM)。高价态主要通过优化电子轨道填充、促进金属d带与氧p带之间的电荷转移来提高OER性能。此外,HVO通常显示出升高的O 2p带,这触发晶格氧作为氧化还原中心,并实施有效的LOM途径以打破AEM的“比例”限制。此外,由整体电荷中性诱导产生的氧空位也促进了LOM中的直接氧耦合。然而,HVO的合成存在相对较大的热力学势垒,这使得它们的制备困难。因此,讨论了HVO的合成策略,以指导HVO电催化剂的进一步设计。最后,概述了在能量转换和存储中的潜在应用面临的进一步挑战和前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d5a/10401147/dd5840501703/ADVS-10-2301706-g009.jpg

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