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Ultralong cycle stability of aqueous zinc-ion batteries with zinc vanadium oxide cathodes
Author(s) -
Lulu Wang,
KuoWei Huang,
Jitao Chen,
Junrong Zheng
Publication year - 2019
Publication title -
science advances
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.928
H-Index - 146
ISSN - 2375-2548
DOI - 10.1126/sciadv.aax4279
Subject(s) - vanadium oxide , materials science , hydronium , cathode , electrochemistry , vanadium , zinc , electrolyte , intercalation (chemistry) , aqueous solution , chemical engineering , energy storage , inorganic chemistry , ion , electrode , chemistry , metallurgy , thermodynamics , power (physics) , physics , organic chemistry , engineering
Hierarchically porous zinc vanadium oxide cathodes contribute to high-rate and ultralong-life aqueous rechargeable zinc batteries. Rechargeable aqueous zinc-ion batteries are promising candidates for large-scale energy storage but are plagued by the lack of cathode materials with both excellent rate capability and adequate cycle life span. We overcome this barrier by designing a novel hierarchically porous structure of Zn-vanadium oxide material. This Zn0.3V2O5·1.5H2O cathode delivers a high specific capacity of 426 mA·h g−1 at 0.2 A g−1 and exhibits an unprecedented superlong-term cyclic stability with a capacity retention of 96% over 20,000 cycles at 10 A g−1. Its electrochemical mechanism is elucidated. The lattice contraction induced by zinc intercalation and the expansion caused by hydronium intercalation cancel each other and allow the lattice to remain constant during charge/discharge, favoring cyclic stability. The hierarchically porous structure provides abundant contact with electrolyte, shortens ion diffusion path, and provides cushion for relieving strain generated during electrochemical processes, facilitating both fast kinetics and long-term stability.

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