Authors
Gaoyuan Liu, Wei Jia, Xinxin Yin, Biao Yang, Jing Xie, Jindou Hu, Zhenjiang Lu, Yali Cao
Published in
Small (Weinheim an der Bergstrasse, Germany). Pages e2500441. Apr 24, 2025. Epub Apr 24, 2025.
Abstract
Amorphous materials, which bear unique atomic arrangements, have garnered significant study on lithium-ion batteries due to inherent properties, including isotropy and defect distribution. Herein, a novel amorphous MoO2- x@V2O3- x@C double-core-shell structure is ingeniously designed by simple solvothermal and pyrolytic reactions, and the valence states of amorphous MoO2 and V2O3 are precisely characterized using X-ray absorption near-edge structure spectroscopic measurements. In situ XRD, in situ EIS and density functional theory calculations confirm that the amorphous structure enhances the electronic conductivity of MoO2- x@V2O3- x@C-2, optimizes the Li+ relocation paths and the associated energy barriers, thus improving the Li+ diffusion kinetics. Furthermore, the formation of V2O3- x layer, along with the establishment of a 3D network structure of amorphous carbon, enhanced the electronic conductivity and mitigated swelling of the electrodes, thereby improving stability during battery cycling. Benefiting from this multiscale coordinated design, the optimized MoO2- x@V2O3- x@C electrodes exhibit high discharge capacity of 477.5 mAh g-1 at 10.0 A g-1, along with exceptional cycling stability, showing minimal capacity loss even after undergoing 1000 cycles at 20.0 A g-1. Additionally, MoO2- x@V2O3- x@C||LiCoO2 full batteries maintain good capacity over 300 cycles. The proposed amorphous and core-shell structure fabrication concept offers novel insights into developing advanced high-efficiency energy storage materials.
PMID:
40270324
Bibliographic data and abstract were imported from PubMed on 24 Apr 2025.
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