4.8 Article

Cation- deficient Zn0.3(NH4)0.3V4O10•0.91H2O for rechargeable aqueous zinc battery with superior low- temperature performance

Journal

ENERGY STORAGE MATERIALS
Volume 38, Issue -, Pages 389-396

Publisher

ELSEVIER
DOI: 10.1016/j.ensm.2021.03.025

Keywords

Aqueous zinc batteries; Ammonium vanadate; Cation-deficient; Cyclability; Low temperature

Funding

  1. National Natural Science Foundation of China [21875226, 52072352, U20A2072]
  2. Foundation for the Youth S&T Innovation Team of Sichuan Province [2020JDTD0035]
  3. Tianfu Rencai Plan
  4. Science Foundation for Distinguished Young Scholars of Sichuan Province [2017JQ0036]
  5. Chengdu Talent plan, Science and Technology Projects for Administration for Market Regulation of Sichuan Province [SCSJ2020016]
  6. Talent Plan of China Science City

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A novel cation-deficient nonstoichiometric Zn-0.3(NH4)(0.3)V4O10·0.91H2O (ZNV) cathode material for aqueous zinc batteries (AZBs) was reported in this research, exhibiting high discharge capacity and superior cycle stability. Both experiments and theoretical simulations demonstrated that the presence of cation vacancies facilitates Zn2+ diffusion during cycles.
The development of aqueous zinc batteries (AZBs) has attracted great attention owing to intrinsic safety, environmental friendliness and low cost. Cathode materials with high capacity and long cycle life at both room temperature and low temperature are urgently needed for practical application of AZBs. Herein, we report cation-deficient nonstoichiometric Zn-0.3(NH4)(0.3)V4O10 center dot 0.91H(2)O(ZNV) cathode materials for AZBs. The pre-intercalated Zn2+ and structural water act as pillars to improve the structure stability. The structural water molecules also provide charge shielding for Zn2+ insertion/extraction. Both experiments and theoretical simulations demonstrate that the presence of cation vacancies facilitates Zn2+ diffusion during cycles. As a result, the ZNV exhibits a high discharge capacity of 461.1 mAh g(-1) at 0.1 A g(-1), and negligible decay after 2000 cycles at 2 A g(-1). Superior cyclability is also achieved at the low temperature (0, -15, and -30 degrees C) with more than 90% capacity retentions over 3500 cycles at 2 A g(-1). In addition, the reversible Zn2+ (de)intercalation reaction mechanism in ZNV is confirmed. Our work may shed a light on the electrode materials designing and development for wide-temperature AZBs.

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