Self-Assembly-Induced Alternately Stacked Single-Layer MoS2 and N-doped Graphene: A Novel van der Waals Heterostructure for Lithium-Ion Batteries

材料科学 阳极 石墨烯 单层 范德瓦尔斯力 异质结 化学工程 纳米技术 锂(药物) 纳米复合材料 兴奋剂 电极 光电子学 分子 物理化学 有机化学 医学 化学 内分泌学 工程类
作者
Chenyang Zhao,Xu Wang,Junhua Kong,Jia Ming Ang,Pooi See Lee,Zhaolin Liu,Xuehong Lu
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:8 (3): 2372-2379 被引量:208
标识
DOI:10.1021/acsami.5b11492
摘要

In this article, a simple self-assembly strategy for fabricating van der Waals heterostructures from isolated two-dimensional atomic crystals is presented. Specifically, dopamine (DOPA), an excellent self-assembly agent and carbon precursor, was adsorbed on exfoliated MoS2 monolayers through electrostatic interaction, and the surface-modified monolayers self-assembled spontaneously into DOPA-intercalated MoS2. The subsequent in situ conversion of DOPA to highly conductive nitrogen-doped graphene (NDG) in the interlayer space of MoS2 led to the formation of a novel NDG/MoS2 nanocomposite with well-defined alternating structure. The NDG/MoS2 was then studied as an anode for lithium-ion batteries (LIBs). The results show that alternating arrangement of NDG and MoS2 triggers synergistic effect between the two components. The kinetics and cycle life of the anode are greatly improved due to the enhanced electron and Li(+) transport as well as the effective immobilization of soluble polysulfide by NDG. A reversible capacity of more than 460 mAh/g could be delivered even at 5 A/g. Moreover, the abundant voids created at the MoS2-NDG interface also accommodate the volume change during cycling and provide additional active sites for Li(+) storage. These endow the NDG/MoS2 heterostructure with low charge-transfer resistance, high sulfur reservation, and structural robustness, rendering it an advanced anode material for LIBs.
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