析氧
电催化剂
价(化学)
氧气
化学物理
分解水
催化作用
材料科学
氧化还原
过渡金属
化学
纳米技术
无机化学
电极
物理化学
电化学
生物化学
有机化学
光催化
作者
Hao Wang,Tingting Zhai,Yifan Wu,Tao Zhou,Binbin Zhou,Congxiao Shang,Zhengxiao Guo
标识
DOI:10.1002/advs.202301706
摘要
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 eg -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.
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