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Aqueous zinc-ion batteries are highly favored for grid-level energy storage owing to their low cost and high safety, but their practical application is limited by slow ion migration. To address this, a strategy has been developed to create a cation-accelerating electric field on the surface of the cathode to achieve ultrafast Zn2+ diffusion kinetics. By employing electrodeposition to coat MoS2 on the surface of BaV6O16 center dot 3H(2)O nanowires, the directional built-in electric field generated at the heterointerface acts as a cation accelerator, continuously accelerating Zn2+ diffusion into the active material. The optimized Zn2+ diffusion coefficient in CC@BaV6O16 center dot 3H(2)O@MoS2 (7.5 x 10(-8) cm(2) s(-1)) surpasses that of most reported V-based cathodes. Simultaneously, MoS2 serving as a cathodic armor extends the cycling life of the Zn-CC@BaV6O16 center dot 3H(2)O@MoS2 full batteries to over 10000 cycles. This work provides valuable insights into optimizing ion diffusion kinetics for high-performance energy storage devices. (c) 2024 Science Press and Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by ELSEVIER B.V. and Science Press. All rights are reserved, including those for text and data mining, AI training, and similar technologies.
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JOURNAL OF ENERGY CHEMISTRY
ISSN: 2095-4956
Year: 2024
Volume: 100
Page: 377-384
1 4 . 0 0 0
JCR@2023
CAS Journal Grade:1
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ESI Highly Cited Papers on the List: 0 Unfold All
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