材料科学
石墨烯
氮化钒
硫黄
化学工程
阴极
锂(药物)
吸附
催化作用
量子点
氮化物
纳米技术
无机化学
化学
有机化学
工程类
图层(电子)
医学
内分泌学
冶金
物理化学
作者
Fu Li,Mengjie Zhang,Wenyan Chen,Xin Cai,Huashang Rao,Jian Chang,Yueping Fang,Xinhua Zhong,Yu Yang,Zhuohong Yang,Xiaoyuan Yu
标识
DOI:10.1021/acsami.1c08113
摘要
Lithium-sulfur batteries (LSBs) have been considered as potential next-generation energy storage systems due to their high specific energy of 2600 Wh kg-1 and 2800 Wh L-1. Nevertheless, the practical application of LSBs still faces several hazards, including the shuttle effect of soluble lithium polysulfides, low electrical conductivities of solid sulfur and lithium sulfides, and large volume expansion during charge/discharge cycles. To address this critical challenge, we innovatively proposed facile synthesis of nanostructured VN quantum dots (VNQD)/holey graphene matrix for stabilizing the sulfur cathode by simultaneously promoting the trapping, anchoring, and catalyzing efficiencies of both LiPSs and Li2S. Benefiting from abundant edge catalytic sites of VNQD, in-plane nanopores of graphene, and high electrical conductivity, the sulfur host not only provides high adsorption capability toward soluble polysulfides, strong binding ability for anchoring solid Li2S, and their rapid conversion kinetics but also contributes abundant sulfur storage sites and efficient transport pathways for lithium ions (Li+) and electrons. Consequently, the sulfur cathode exhibits high initial capacities of 1320 mAh g-1, high rate capability (850 mAh g-1 @ 4 mA cm-2), and high capacity retention of 99.95% per cycle after 500 cycles, providing a feasible solution for the practical utilization of shuttle-free Li-S batteries.
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