4.7 Article

Chrysanthemum-like Polyaniline-Anchored PANI0.22?V2O5?0.88H2O-Hybridized Cathode for High-Stable Aqueous Zinc-Ion Batteries

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ACS APPLIED ENERGY MATERIALS
卷 6, 期 5, 页码 3102-3112

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsaem.3c00063

关键词

aqueous zinc-ion batteries; chrysanthemum-like microstructure; polyaniline-intercalation; Zn2+; H plus hybrid mechanism

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Based on the charge intercalation mechanism, an original chrysanthemum-like organic conductive polyaniline (PANI) intercalated hybridized cathode (PANI0.22 center dot V2O5 center dot 0.88H2O) is developed. The electrostatic interactions between Zn2+ and the V-O layer can be effectively weakened due to the pillars effects and unique pi-conjugated structure of PANI. The 3D micromorphology provides abundant active sites for Zn2+ transfer and intimate contact with electrolytes. The chrysanthemum-like PANI-intercalated V2O5 exhibits a high specific capacity and excellent cycling stability.
Based on the charge intercalation mechanism, an optimized regulation of the interlayer spacing and micromorphology is crucial to achieving promoted Zn2+ storage performance for the affordable layered vanadium oxides. Herein, an original chrysanthemum-like organic conductive polyaniline (PANI) intercalated hybridized cathode (PANI0.22 center dot V2O5 center dot 0.88H2O) is developed by preintercalation of the aniline monomer and subsequently in situ polymerization within the oxide interlayers. Profiting from the pillars effects as well as the unique pi-conjugated structure of PANI, the electrostatic interactions between the Zn2+ and the V-O layer can be effectively weakened. More importantly, the conjugated conductive guest polymer could inherently induce electron transfer to lower the valence of vanadium, which is beneficial for enhancing electronic conductivity. Moreover, the 3D micromorphology guarantees abundant active sites for Zn2+ transfer and intimate contact with electrolytes. Accordingly, the chrysanthemum-like PANI-intercalated V2O5 exhibits a high specific capacity of 447 mA h g-1 at 0.1 A g-1 and state-of-the-art cycling stability at 92% capacity retention after 3000 cycles. Also, the meticulous charge storage mechanism of this hybrid cathode is investigated systematically through a series of in-depth analyses. Our findings provide a pathway for tuning the interlayer spacing and microstructure toward advanced multivalent ion storage applications.

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