4.8 Article

Ultrafast Rechargeable Aqueous Zinc-Ion Batteries Based on Stable Radical Chemistry

Journal

ADVANCED FUNCTIONAL MATERIALS
Volume 31, Issue 33, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adfm.202102011

Keywords

aqueous zinc-ion batteries; energy storage; fast charging; organic cathodes; radical intermediates

Funding

  1. Beijing Municipal Natural Science Foundation [2204083]
  2. National Natural Science Foundation of China [21972007, 51822201, 51902013]
  3. China Postdoctoral Science Foundation [BX20180021, 2019M650428]
  4. high performance computing (HPC) resource at Beihang University

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Aqueous zinc-ion batteries (ZIBs) show great promise as fast-charging energy-storage systems due to their attractive ionic conductivity, high theoretical energy density, and low cost. This study demonstrates stable radical intermediate generation in a typical organic electrode material (methylene blue [MB]), which effectively enhances the intrinsic kinetics of the cathode and enables ultrafast Zn2+ storage. Anionic co-intercalation helps maintain the stability of the structure, resulting in excellent rate capability and long cycle life for Zn-MB batteries.
Aqueous zinc-ion batteries (ZIBs) are a promising candidate for fast-charging energy-storage systems due to its attractive ionic conductivity of water-based electrolyte, high theoretical energy density, and low cost. Current strategies toward high-rate ZIBs mainly focus on the improvement of ionic or electron conductivity within cathodes. However, enhancing intrinsic electrochemical reaction kinetics of active materials to achieve fast Zn2+ storage has been greatly omitted. Herein, for the first time, stable radical intermediate generation is demonstrated in a typical organic electrode material (methylene blue [MB]), which effectively decreases the reaction energy barrier and enhances the intrinsic kinetics of MB cathode, enabling ultrafast Zn2+ storage. Meanwhile, anionic co-intercalation essentially avoids MB molecules rearranging their configuration and sharing Zn2+ with adjacent functional groups, thus keeps the structure stable. As a result, Zn-MB batteries exhibit an excellent rate capability up to 500C and ultralong life of 20 000 cycles with a negligible 0.07% capacity decay per cycle at 100C, which is superior to that of most reported aqueous ZIBs batteries. This work provides a novel strategy of stable radical chemistry for ultrafast-charging aqueous ZIBs, which can be introduced to other appropriate organic materials and multivalent ion battery systems.

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