2D MoS2/polyaniline heterostructures with enlarged interlayer spacing for superior lithium and sodium storage

被引:100
|
作者
Wang, Haiyan [1 ]
Jiang, Hao [1 ]
Hu, Yanjie [1 ]
Li, Neng [2 ]
Zhao, Xiujian [2 ]
Li, Chunzhong [1 ]
机构
[1] East China Univ Sci & Technol, Sch Mat Sci & Engn, AKey Lab Ultrafine Mat, Minist Educ, Shanghai 200237, Peoples R China
[2] Wuhan Univ Technol, State Key Lab Silicate Mat Architectures, Wuhan 430070, Peoples R China
基金
中国国家自然科学基金;
关键词
EXCELLENT ELECTROCHEMICAL PERFORMANCE; TOTAL-ENERGY CALCULATIONS; ION BATTERY; CARBON NANOFIBERS; HIGH-CAPACITY; MOS2; ANODE; PLANE; NANOARCHITECTURES; MONOLAYERS;
D O I
10.1039/c7ta00030h
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
The exploitation of high-capacity and long-life MoS2-based materials is highly important for developing lithium ion batteries (LIBs) and sodium ion batteries (SIBs). Herein, we demonstrate the confined synthesis of 2D MoS2/ polyaniline (MoS2/PANI) nanosheet heterostructures with well-defined interfaces, in which the interlayer distance of MoS2 is greatly enlarged from 0.62 nm to 1.08 nm. The introduction of such a big interlayer distance for efficient Li+/Na+ storage has never been demonstrated before. The unique MoS2/PANI nanosheets can address well the key challenges of traditional MoS2 anode materials related to low conductivity particularly in the vertical direction, easy restacking/aggregation, large volumetric change and sluggish Li+/Na+ diffusion kinetics in the interlamination. Consequently, they deliver a high reversible capacity, superior rate capability and long cycle life for both LIBs and SIBs. A state-of-the-art ab initio molecular dynamics (AIMD) simulation also reveals that MoS2/PANI nanosheets with enlarged interlayer spacing possess a remarkably improved Li+/Na+ diffusion mobility compared to pristine MoS2 nanosheets. The present material design concept opens new directions for finding efficient LIBs/SIBs anodes with high capacity, rate capability and stability.
引用
收藏
页码:5383 / 5389
页数:7
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