碳化钒
氧化钒
钒
锂硫电池
材料科学
碳纤维
硫黄
电池(电)
锂(药物)
异质结
氧化物
化学工程
磷酸钒锂电池
无机化学
纳米技术
化学
阳极
电极
电化学
光电子学
复合数
冶金
复合材料
功率(物理)
物理化学
医学
物理
量子力学
工程类
内分泌学
作者
Dong Mao,Yifan Fu,Junjie Ba,Junpeng Li,Xiuxiu Yin,Chunzhong Wang,Yingjin Wei,Yizhan Wang
标识
DOI:10.1016/j.jcis.2025.137646
摘要
Lithium-sulfur (Li-S) batteries hold great promise due to their high theoretical energy density, but their practical application is impeded by the insulating nature of sulfur and the shuttle effect of soluble lithium polysulfides. Herein, we report the synthesis of vanadium carbide/oxide heterostructures embedded in a two-dimensional carbon matrix (VC/V2O3@C) through a facile topological transformation strategy to address these challenges. The synergistic heterostructure combines strong polysulfide adsorption capability with excellent redox activity. In situ Raman spectroscopy reveals that the VC/V2O3@C composite significantly accelerates polysulfide conversion and suppresses the shuttle effect. As a result, Li-S batteries utilizing VC/V2O3@C exhibit a high discharge specific capacity of 1281 mAh g-1 at 0.5 C and excellent cycling stability with a low capacity decay rate of 0.045 % per cycle (1200 cycles) at 1 C. Even under high sulfur loading and lean electrolyte conditions, impressive areal capacities are achieved. This work demonstrates a novel approach to enhancing Li-S battery performance through synergistic heterostructure design.
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