4.7 Article

Long-Life Zinc/Vanadium Pentoxide Battery Enabled by a Concentrated Aqueous ZnSO4 Electrolyte with Proton and Zinc Ion Co-Intercalation

期刊

ACS APPLIED ENERGY MATERIALS
卷 3, 期 11, 页码 11183-11192

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsaem.0c02126

关键词

rechargeable zinc batteries; V2O5 cathode; H+ and Zn2+ co-intercalation; aqueous ZnSO4 electrolyte; nonaqueous electrolyte

资金

  1. Natural Science Foundation of Hebei Province [B202001001, B2019201160]
  2. National Natural Science Foundation of China [21805066, 22075067, 22075016]
  3. Top Young Talents Project of Hebei Education Department [BJ2019052]
  4. China Postdoctoral Science Foundation [2019T120191, 2018M640244]
  5. Chunhui Program of Ministry of Education of China
  6. Young Eli te Scient ists Sponsorship Program by CAST [2018QNRC001]
  7. Advanced Talents Incubation Program of Hebei University [521000981138]
  8. 111 Project [B12015]

向作者/读者索取更多资源

Rechargeable aqueous zinc/vanadium pentoxide (Zn/V2O5) battery chemistry has recently attracted a great attention due to its high safety, material abundance, cost effectiveness, and desirable energy density. However, the reaction mechanism of V2O5 in an aqueous electrolyte remains a topic of discussion, and the limited life span resulting from the active materials dissolution hinders the further development of the Zn/V2O5 battery. Here, we report a long-life aqueous Zn/V2O5 battery using a simply ball-milled V2O5 cathode, a concentrated aqueous ZnSO4 electrolyte, and a metallic Zn anode. Electrochemical, structural, and spectroscopic analyses reveal that the V2O5 electrode experiences a highly reversible proton (H+) and Zn2+ co-intercalation mechanism in aqueous media, which differs from the conventional cognition that Zn2+ ion as the only charge carrier inserts into the V2O5 host. The electrolyte-involved (dis)appearance of zinc sulfate hydroxide on the electrodes' surface caused by Fr (de)intercalation has also been clarified. In addition, the optimized 3 M ZnSO4 electrolyte can not only suppress the dissolution of the V2O5 cathode but also enhance the stability of the Zn anode, thereby enabling the stable operation of the Zn/V2O5 battery with a reversible capacity of 357 mAh g(-1) after 2000 cycles without obvious decay at 2.0 A g(-1). This work opens up frontiers in the mechanism insight and electrolyte formulation for aqueous Zn batteries.

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