Abstract

Aqueous rechargeable zinc-ion batteries (ARZIBs) are promising candidates for fast-charging energy-storage systems. The issues of stronger interactions between Zn2+ and the cathode for ultrafast ARZIBs can be partially addressed by enhancing mass transfer and ion diffusion of the cathode. Herein, via thermal oxidation for the first time, N-doped VO2 porous nanoflowers with short ion diffusion paths and improved electrical conductivity were synthesized as ARZIBs cathode materials. The introduction of nitrogen derived from the vanadium-based-zeolite imidazolyl framework (V-ZIF) contributes to enhanced electrical conductivity and faster ion diffusion, while the thermal oxidation of the VS2 precursor assists the final product in exhibiting a more stable three-dimensional nanoflower structure. In particular, the N-doped VO2 cathode shows excellent cycle stability and superior rate capability with the delivered capacities of 165.02 mAh g−1 and 85 mAh g−1, at 10 A g−1 and 30 A g−1, and the capacity retention of 91.4% after 2200 cycles and 99% after 9000 cycles, respectively. Remarkably, the battery takes less than 10 s to be fully charged at 30 A g−1. Hence, this work provides a new avenue for designing unique nanostructured vanadium oxides and developing electrode materials suitable for ultrafast charging.

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