Self-assembled α-MnO2 urchin-like microspheres as a high-performance cathode for aqueous Zn-ion batteries

Aqueous Zn-ion batteries (AZIBs) are one of the promising battery technologies for the green energy storage and electric vehicles. As one attractive cathode material for AZIBs, α-MnO 2 materials exhibit superior electrochemical properties. However, their long-term reversibility is still in great sus...

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Published inScience China materials Vol. 63; no. 7; pp. 1196 - 1204
Main Authors Wu, Yunzhao, Tao, Ye, Zhang, Xianfu, Zhang, Kai, Chen, Shengbin, Liu, Yu, Ding, Yong, Cai, Molang, Liu, Xuepeng, Dai, Songyuan
Format Journal Article
LanguageEnglish
Published Beijing Science China Press 01.07.2020
Springer Nature B.V
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Summary:Aqueous Zn-ion batteries (AZIBs) are one of the promising battery technologies for the green energy storage and electric vehicles. As one attractive cathode material for AZIBs, α-MnO 2 materials exhibit superior electrochemical properties. However, their long-term reversibility is still in great suspense. Considering the decisive effect of the structure and morphology on the α-MnO 2 materials, hierarchical α-MnO 2 materials would be promising to improve the cycle performance of AZIB. Here, we synthesized the α-MnO 2 urchin-like microspheres (AUM) via a self-assembled method. The porous microspheres composed of one-dimensional α-MnO 2 nanofibers with high crystallinity, which improved the surface area and active sites for Zn 2+ intercalation. The AUM-based AZIB realized a high initial capacity of 308.0 mA h g −1 and the highest energy density was 396.7 W h kg −1 The kinetics investigation confirmed the high capacitive contribution and fast ion diffusion of the AUM. Ex-situ XRD measurement further verified the synergistic insertion/extraction of H + and Zn 2+ ions during the charge/discharge process. The superiority of the AUM guaranteed good electrochemical performance and reversible phase evolution, and this application would promote the follow-up research on the advanced AZIB.
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ISSN:2095-8226
2199-4501
DOI:10.1007/s40843-020-1293-8