Yang Liu
;
Chengjie Lu
;
Yunting Yang
;
Wenshu Chen
;
Fei Ye
;
Hongliang Dong
;
Yuping Wu
;
Renzhi Ma
;
Linfeng Hu
Description:
(abstract)Aqueous zinc-ion battery shows great potential and considerable interest in the energy storage field, and the nanoconfinement of cations in layered oxide cathode is an important approach to realize advanced zinc ion storage on capacity and cycling stability. However, thus far, the conventional hydrothermal/solvothermal route for this nanoconfinement has been restricted to its uncontrollable phase structure and the difficulty on the multiple cation co-confinement simultaneously. Herein, we reported a general, supramolecular self-assembly of ultrathin V2O5 nanosheets using various unitary cations including Na+, K+, Mg2+, Ca2+, Zn2+, Al3+, NH4+ and multiple cations (NH4+ + Na+, NH4+ + Na+ + Ca2+, NH4+ + Na+ + Ca2+ +Mg2+). The unitary cation confinement results in a remarkable increase in the specific capacity and Zn-ion diffusion kinetics, and the multiple cation confinement gives rise to superior structural and cycling stability by multiple cation synergetic pillaring effect. The optimized diffusion coefficient of Zn-ion (7.5×10-8 cm2 s-1) in this assembly series surpasses most of the V-based cathodes reported up to date. Density functional theoretical (DFT) simulation further reveals a declined Zn-ion diffusion barrier by cation confinement due to a significantly weakened interaction between Zn2+ and the dangling oxygen atom of V2O5. Our work develops a novel multiple-cations nanoconfinement strategy toward high-performance cathode for aqueous battery. It also provides new insights into the guest cation regulation of zinc-ion diffusion kinetics through a general, supramolecular assembly pathway.
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Keyword: Nanosheets, Battery
Date published: 2024-01-29
Publisher: Wiley
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Funding:
Manuscript type: Author's version (Accepted manuscript)
MDR DOI: https://doi.org/10.48505/nims.4537
First published URL: https://doi.org/10.1002/adma.202312982
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Updated at: 2025-01-29 12:30:19 +0900
Published on MDR: 2025-01-29 12:30:20 +0900
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