4.6 Article

Relieving hydrogen evolution and anodic corrosion of aqueous aluminum batteries with hybrid electrolytes

Journal

JOURNAL OF MATERIALS CHEMISTRY A
Volume 10, Issue 9, Pages 4739-4748

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1ta10125k

Keywords

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Funding

  1. National Natural Science Foundation of China [22005207]
  2. Guangdong Basic and Applied Basic Research Foundation [2019A1515011819]
  3. China Postdoctoral Science Foundation [2019M650881]
  4. Youth Program of National Natural Science Foundation of China [21905300]
  5. Key R&D Project of Shandong Province [2019GGX103032]
  6. Fundamental Research Funds for the Central Universities [21CX06011A]
  7. GRF Scheme [CityU 11305218]

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This study explores the use of an AlCl3/LiTFSI electrolyte for rechargeable aqueous aluminum-ion batteries (AAIBs). The addition of an appropriate concentration of LiTFSI effectively inhibits hydrogen evolution and corrosion of Al anodes. The full AAIB, composed of a vanadium potassium cathode and Al anode, exhibits high capacity, superior rate capability, and outstanding cycling stability in this electrolyte. The soft-packed AAIB also shows good cycling stability and desirable flexibility. The findings of this study may contribute to the development of rechargeable aluminum-ion batteries with aqueous electrolytes.
The lower electro-stripping/plating potential of Al3+/Al (-1.68 V) than that of H+/H-2 seriously impedes the performance of rechargeable aqueous aluminum-ion batteries (AAIBs). Besides, the Al plate is easily corroded in aqueous electrolytes due to the typical acidic nature of aluminum salt solutions. Exploring appropriate aqueous electrolytes is indispensable to achieve a high-performance AAIB. In this work, we initiate an AlCl3/lithium bis(trifluoromethane sulfonyl)imide (LiTFSI) electrolyte and find that the addition of an appropriate concentration of LiTFSI can efficiently hinder the hydrogen evolution and corrosion of Al anodes. The full AAIB composed of a vanadium potassium cathode and Al anode exhibits reversible charge/discharge behaviors in 0.5 M AlCl3@12 M LiTFSI electrolyte. Electrochemical and structural analyses reveal that the vanadium potassium cathode experiences a reversible Al3+, H+ and Li+ co-intercalation/de-intercalation process during cycling. The full AAIB manifests excellent performance in terms of large capacity (223 mA h g(-1) at 1000 mA g(-1)), superior rate capability (more than 50% retention from 1000 to 6000 mA g(-1)) and outstanding cycling stability (maintains 64.6% after 300 cycles). Moreover, the soft-packed AAIB also manifests good cycling stability and desirable flexibility. The strategy reported in our manuscript may promote the development of rechargeable aluminum-ion batteries based on aqueous electrolytes.

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