Authors
Zhen Cui, Ailing Song, Zirui Cui, Manman Duanmu, Zhipeng Ma, Hao Liu, Guangjie Shao, Xinyi Tan, Guoxiu Wang, Hao Tian
Published in
Advanced science (Weinheim, Baden-Wurttemberg, Germany). Pages e78316. Oct 18, 2026. Epub Oct 18, 2026.
Abstract
CeO2-based electrocatalysts are promising for the oxygen evolution reaction (OER) owing to their distinctive Ce3+/Ce4+ redox flexibility, large oxygen-storage capacity, and lattice adaptability. More importantly, CeO2 can dynamically regulate catalyst surface reconstruction and electronic structure while significantly enhancing catalytic activity and long-term stability. In this review, we first focus on CeO2-based electrocatalysts for OER from structural characteristics, design principles and strategies, structure-property relationships, interfacial structure, as well as critical evaluation of design strategies and selection principles. The mechanistic roles of CeO2 in OER are highlighted, including redox chemistry and oxygen-vacancy (Ov) dynamics, electronic-structure modulation and charge transfer, interfacial coupling and surface reconstruction, as well as operando evidence and the controversy over lattice-oxygen participation. The performance of CeO2-based OER electrocatalysts in different electrolytes, including alkaline, acidic, and seawater media, is also summarized to demonstrate their applicability under diverse operating conditions. Finally, from the perspectives of electronic-structure evolution, redox-state transitions, lattice evolution, and catalytic pathways, this review summarizes the underlying mechanisms by which CeO2 regulates the dynamic catalytic behavior of OER and provides an outlook on future design strategies for developing highly efficient and durable CeO2-based electrocatalysts.
PMID:
42893448
Bibliographic data and abstract were imported from PubMed on 18 Oct 2026.
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