氧化钒
钒
阴极
水溶液
材料科学
氧化物
电化学
无机化学
碳纤维
化学工程
电导率
过渡金属
电极
化学
催化作用
冶金
复合材料
物理化学
复合数
工程类
生物化学
作者
Ruona Liu,Junye Zhang,Huang Chen,Ciqing Dong,Le Xu,Bo Zhu,Linlin Wang,Ling Zhang,Luyang Chen
标识
DOI:10.1016/j.jcis.2023.09.045
摘要
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 Mn2+ 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 Mn2+ inserted between interlayers, provides more active sites, higher electronic conductivity, and faster ion diffusion. In addition, GHC reinforces the integrity of external structure, while Mn2+ 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.
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