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Boosted Zn2+ storage performance of hydrated vanadium oxide by defect and heterostructure
Journal of Materials Chemistry A ( IF 10.7 ) Pub Date : 2022-06-09 , DOI: 10.1039/d2ta03389e
Viet Phuong Nguyen 1, 2 , Ji Su Park 3 , Jong Min Yuk 3 , Minsub Oh 2 , Jae-Hyun Kim 1, 2 , Seung-Mo Lee 1, 2
Affiliation  

The inherent sluggish Zn2+ diffusion and poor electronic conductivity limit the ion intercalation/deintercalation process in aqueous Zn-ion batteries (ZIBs) using an oxide-based cathode. Here, we demonstrated that a heterostructure in the form of defective hydrated vanadium oxide embedded in the porous carbon textile (d-VOH@CT) could tackle these issues. The additional edges created by crystal defects significantly promoted facile Zn-ion adsorption and intercalation. Expanded interlayer spacing and reduced crystalline domain size kinetically facilitated fast Zn-ion diffusion in d-VOH flakes with shortened diffusion paths. Moreover, the heterostructure of d-VOH on the conductive carbon textile triggered rapid charge transfer, leading to high rate capability and structural stability. The ZIBs fabricated using the d-VOH@CT cathode delivered a preferable reversible capacity of 416 mA h g−1 at 0.1 A g−1, an impressive energy density of 293 W h kg−1 and long cycle life. In addition, the d-VOH@CT heterostructure was able to be used as a freestanding cathode for a flexible ZIB with outstanding mechanical robustness and electrochemical stability.

中文翻译:

通过缺陷和异质结构提高水合氧化钒的 Zn2+ 存储性能

固有的呆滞 Zn 2+扩散和较差的电子导电性限制了使用氧化物阴极的水系锌离子电池 (ZIB) 中的离子嵌入/脱嵌过程。在这里,我们证明了嵌入多孔碳织物(d-VOH@CT)中的有缺陷的水合氧化钒形式的异质结构可以解决这些问题。晶体缺陷产生的额外边缘显着促进了锌离子的吸附和嵌入。扩大的层间距和减小的晶畴尺寸在动力学上促进了 d-VOH 薄片中的快速 Zn 离子扩散,并缩短了扩散路径。此外,d-VOH 在导电碳织物上的异质结构引发了快速的电荷转移,从而获得了高倍率性能和结构稳定性。-1 at 0.1 A g -1 ,293 W h kg -1的惊人能量密度和长循环寿命。此外,d-VOH@CT 异质结构能够用作柔性 ZIB 的独立阴极,具有出色的机械鲁棒性和电化学稳定性。
更新日期:2022-06-14
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