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通过包覆葡萄糖水热碳和预嵌入Mn(II)离子对水合氧化钒正极进行氧缺陷工程和结构强化用于高容量水系锌离子电池

Oxygen defects engineering and structural strengthening of hydrated vanadium oxide cathode by coating glucose hydrothermal carbon and pre-embedding Mn (II) ion for high-capacity aqueous zinc ion batteries.

作者信息

Liu Ruona, Zhang Junye, Huang Chen, Dong Ciqing, Xu Le, Zhu Bo, Wang Linlin, Zhang Ling, Chen Luyang

机构信息

Key Laboratory for Ultrafine Materials of Ministry of Education, School of Materials Science and Engineering, East China University of Science and Technology, Shanghai 200237, China.

Institute for Sustainable Energy/College of Science, Shanghai University, Shanghai 200444, China.

出版信息

J Colloid Interface Sci. 2024 Jan 15;654(Pt A):279-288. doi: 10.1016/j.jcis.2023.09.045. Epub 2023 Sep 9.

DOI:10.1016/j.jcis.2023.09.045
PMID:37844499
Abstract

Vanadium oxide-based cathode with unique layered structure is considered as a candidate for aqueous zinc ion batteries (AZIBs). Unfortunately, considering poor electronic conductivity, sluggish diffusion kinetics, and the destruction of layered structures in the cycling process, the actual capacity and rate capability are constrained. Herein, the glucose hydrothermal carbon (GHC) and transition metal Mn ion have been utilized to incorporate hydrated vanadium oxide (Mn-VOH@GHC). The oxygen vacancies defects of VOH, induced by GHC anchored on surface and Mn inserted between interlayers, provides more active sites, higher electronic conductivity, and faster ion diffusion. In addition, GHC reinforces the integrity of external structure, while Mn ion acts as structural pillars to support the interlayer structure. The Mn-VOH@GHC electrode can produce a high capacity of 530 mAh/g at the current density of 0.2 A/g thanks to these crucial properties, and after 2000 cycles at a high current density of 2 A/g, it can also produce a reversible capacity of 344 mAh/g. The results suggest that the synergistic effect of defect engineering and metal ion pre-insertion provides a new idea in enhancement of the electrochemical performance of AZIBs cathode materials.

摘要

具有独特层状结构的氧化钒基阴极被认为是水系锌离子电池(AZIBs)的候选材料。不幸的是,由于电子导电性差、扩散动力学缓慢以及循环过程中层状结构的破坏,其实际容量和倍率性能受到限制。在此,利用葡萄糖水热碳(GHC)和过渡金属锰离子制备了水合氧化钒复合材料(Mn-VOH@GHC)。GHC锚固在表面以及Mn插入层间诱导产生的VOH氧空位缺陷,提供了更多的活性位点、更高的电子导电性和更快的离子扩散速率。此外,GHC增强了外部结构的完整性,而Mn离子作为结构支柱支撑层间结构。得益于这些关键特性,Mn-VOH@GHC电极在0.2 A/g的电流密度下可产生530 mAh/g的高容量,在2 A/g的高电流密度下循环2000次后,仍可产生344 mAh/g的可逆容量。结果表明,缺陷工程和金属离子预插入的协同效应为提高AZIBs阴极材料的电化学性能提供了新思路。

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