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用于高面积容量锂硫电池的0D-2D多功能双金属MOF衍生物-MXene异质结

0D-2D multifunctional bimetallic MOF derivative-MXene heterojunction for high areal capacity lithium-sulfur batteries.

作者信息

Wang Jinxin, Zhang Yongzheng, Chen Zixin, Zhou Zhiqiang, Wang Jitong, Ma Cheng, Qiao Wenming, Xu Zhi, Ling Licheng

机构信息

State Key Laboratory of Chemical Engineering, School of Chemical Engineering, East China University of Science and Technology, Shanghai 200237, China.

State Key Laboratory of Chemical Engineering, School of Chemical Engineering, East China University of Science and Technology, Shanghai 200237, China.

出版信息

J Colloid Interface Sci. 2025 Jan 15;678(Pt C):79-88. doi: 10.1016/j.jcis.2024.09.026. Epub 2024 Sep 7.

Abstract

Lithium-sulfur (Li-S) batteries have attracted much attention due to their high specific capacity. However, at high loads and rates, the polysulfides conversion rate and ion transport of batteries are slow, limiting their commercialization. This work reports zero-dimensional (0D) bimetallic MOF derivatives grown in situ on two-dimensional (2D) MXene by electrostatic adsorption (FeCo@TiC). The 0D bimetallic structure effectively avoids the stacking of MXene while providing a dual catalytic site for polysulfides. The 2D structure of MXene also provides a large number of pathways for the rapid diffusion of lithium ions. This 0D-2D heterostructured heterogeneous catalyst with bimetallic synergistic active sites efficiently immobilizes and catalyzes polysulfides, providing a fast charge transfer pathway for the electrochemical reaction of lithium polysulfides. The Li-S battery with this multifunctional 0D-2D heterojunction structure catalyst has outstanding high rate capacity (703 mAh g at 4 C at room temperature and 555 mAh g at 2 C at 0 °C), fascinating capacity at high load (5.5 mAh cm after 100 cycles at a high sulfur content of 8.2 mg cm). The study provides new ideas for the commercialization of high-efficiency Li-S batteries.

摘要

锂硫(Li-S)电池因其高比容量而备受关注。然而,在高负载和高倍率下,电池中多硫化物的转化率和离子传输速度较慢,限制了它们的商业化。这项工作报道了通过静电吸附在二维(2D)MXene上原位生长的零维(0D)双金属MOF衍生物(FeCo@TiC)。这种0D双金属结构有效地避免了MXene的堆叠,同时为多硫化物提供了双催化位点。MXene的二维结构也为锂离子的快速扩散提供了大量通道。这种具有双金属协同活性位点的0D-2D异质结构非均相催化剂有效地固定并催化多硫化物,为多硫化锂的电化学反应提供了快速电荷转移途径。具有这种多功能0D-2D异质结结构催化剂的锂硫电池具有出色的高倍率容量(室温下4C时为703 mAh g,0°C时2C时为555 mAh g),在高负载下具有令人着迷的容量(在硫含量为8.2 mg cm的高硫负载下100次循环后为5.5 mAh cm)。该研究为高效锂硫电池的商业化提供了新思路。

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