Interfacial coupling metallic MoS2 nanosheets with wrinkled Ti3C2TX MXene for reversible and stable sodium storage

被引:19
|
作者
Liu, Zhimin [1 ]
Tao, Song [1 ]
Han, Jiachen [1 ]
Gao, Zhaoyang [1 ]
Xu, Wenbin [1 ]
Min, Huihua [2 ]
Shen, Xiaodong [1 ]
Yang, Hao [1 ]
Wang, Jin [1 ]
机构
[1] Nanjing Tech Univ, Coll Mat Sci & Engn, Nanjing 211800, Peoples R China
[2] Nanjing Forestry Univ, Elect Microscope Lab, Nanjing 210037, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Molybdenumdisulfide; Transition metal carbides; Heterointerface; Reversible conversion; Sodium-ion batteries; 1T MOS2; ION; CARBON; INTERCALATION; LITHIUM;
D O I
10.1016/j.mtener.2023.101256
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Owing to high electronic conductivity and large interlayer spacing, 1T-MoS2 has attracted remarkable attention as one of the most potential anode materials for sodium-ion batteries. However, the electro-chemical instability seriously hinders its wide application. The high reversible regeneration of Mo-S bonds to pristine 1T-MoS2 inevitably determines electrochemical reversibility of 1T-MoS2. Herein, hi-erarchical 1T-MoS2/MXene architectures demonstrate impressive Na-storage performance with stable reversibility. The theoretical simulation results reveal that the favorable structure of Na-S bonding at Mo/MXene heterointerfaces weakens Na-S bond and thereby decreases the recombination energies of Mo-S bond upon desodiation, greatly promoting reversible Na-storage. Moreover, the ex operando X-ray diffraction and Raman spectra further demonstrate an efficient reversible conversion reaction in 1T-MoS2/MXene anode. Therefore, the heterogenous 1T-MoS2/MXene achieves a considerable perfor-mance as a sodium-ion battery anode material.(c) 2023 Elsevier Ltd. All rights reserved.
引用
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页数:10
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