Journal of Inorganic Materials

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Regulating Electronic Structure and Lithium-storage Kinetics of High-entropy Oxides via Fe-O-Ti Heterointerface Engineering

XIAO Bin, ZHU Haoran, ZOU Peng, WU Gang, XIE Zelin, SUI Yanwei   

  1. School of Materials Science and Physics, China University of Mining and Technology, Xuzhou 221116, China
  • Received:2026-04-23 Revised:2026-07-19
  • About author:XIAO Bin, associate professor. E-mail: binxiao@cumt.edu.cn
  • Supported by:
    National Key R&D Program of China (2024YFE0108500); National Natural Science Foundation of China (52504345); Basic Research Program of Jiangsu (BK20251657); Fundamental and Interdisciplinary Disciplines Breakthrough Plan of the Ministry of Education of China (JYB2025XDXM308); Jiangsu Province Qinglan Project

Abstract: High-entropy oxides (HEOs) show great potential as anode materials for lithium-ion batteries owing to their compositional tunability, synergistic multication redox activity, and rich defect chemistry. However, their practical application is still limited by insufficient intrinsic conductivity and sluggish lithium-storage kinetics. In this work, a (FeZnCrMn)3O4/TiO2 composite with tightly coupled Fe-O-Ti heterointerfaces was constructed via high-energy ball milling followed by high-temperature oxidation and air quenching. Compared with the Ti-incorporated (FeTiZnCrMn)3O4 control sample dominated by a spinel high-entropy oxide phase and the mechanically mixed (FeZnCrMn)3O4-TiO2 control sample, the heterostructured composite exhibits superior rate capability and cycling stability, delivering a discharge capacity of 512.9 mAh·g-1 at 5 A·g-1. The relative peak-area ratio of oxygen-vacancy-related components in the surface O1s X-ray photoelectron spectrum of (FeZnCrMn)3O4/TiO2 reaches 45%, indicating that the formation of heterointerfaces is accompanied by modulation of the surface defect environment. First-principles calculations demonstrate that Fe-O-Ti interfacial bonds induce redistribution of Fe/Ti-related orbitals near the Fermi level and interfacial charge rearrangement, while increasing the density of low-energy electronic states near the conduction-band minimum. The electronic structure reconstruction and defect modulation jointly improve interfacial charge-transfer kinetics and Li+ transport behavior, thereby enhancing high-rate lithium-storage performance. This work provides a reference for the heterointerface engineering of high-entropy oxide anodes.

Key words: high-entropy oxide, heterointerface engineering, Fe-O-Ti bond, lithium-storage kinetics, lithium-ion battery anodes

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