五氧化二铁
电解质
钒
无机化学
水溶液
插层(化学)
溶解
电池(电)
阴极
锌
阳极
氢氧化锌
磷酸钒锂电池
材料科学
化学
电化学
电极
冶金
物理
物理化学
功率(物理)
量子力学
作者
Yang Dong,Ming Jia,Yuanyuan Wang,Jianzhong Xu,Yongchang Liu,Lifang Jiao,Ning Zhang
标识
DOI:10.1021/acsaem.0c02126
摘要
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 H+ (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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