Ultrafast lithium energy storage enabled by interfacial construction of interlayer-expanded MoS2/N-doped carbon nanowires

被引:89
|
作者
Sun, Huanhuan [1 ,2 ]
Wang, Jian-Gan [1 ,2 ,3 ]
Zhang, Yu [3 ]
Hua, Wei [1 ,2 ]
Li, Yueying [1 ,2 ]
Liu, Huanyan [1 ,2 ]
机构
[1] Northwestern Polytech Univ, State Key Lab Solidificat Proc, Ctr Nano Energy Mat, Sch Mat Sci & Engn, Xian 710072, Shaanxi, Peoples R China
[2] Shaanxi Joint Lab Graphene NPU, Xian 710072, Shaanxi, Peoples R China
[3] Hong Kong Univ Sci & Technol, Dept Chem & Biomol Engn, Kowloon, Hong Kong, Peoples R China
基金
中国国家自然科学基金;
关键词
HIGH-PERFORMANCE ANODES; HYBRID AEROGELS; SODIUM STORAGE; ION; COMPOSITES; NANOMATERIALS; NANOSHEETS; DESIGN;
D O I
10.1039/c8ta04852e
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
Two-dimensional (2D) molybdenum disulfide (MoS2) has been extensively regarded as a promising host material for lithium ion batteries due to the reversible insertion of Li+ into the layered structures. However, achieving ultrafast and durable Li+ storage has a challenge of designing largely exposed edge-oriented and kinetically favorable MoS2-based nanostructures. Herein, we report an interfacial synthesis strategy for facile construction of ultrathin MoS2/N-doped carbon nanowires (MoS2/N-C NWs) (ca. 10 m in length) with a largely expanded (002) plane of MoS2 (d = 1.03 nm, vs. bulk 0.62 nm). This hierarchical nanowire configuration composed of edge-oriented and interlayer-expanded MoS2 nanosheets can not only effectively decrease the diffusion energy barriers for Li+ intercalation and improve the number of electrochemically active sites, but also provide fast electron pathways. As an anode for LIBs, the MoS2/N-C NWs demonstrate excellent rate capabilities (600 mA h g(-1) at 5 A g(-1) and 453 mA h g(-1) at 10 A g(-1)) and long-term durability (86.7% retention at 5 A g(-1) over 500 cycles). This study demonstrates the great potential of the MoS2/N-C NWs as promising anode materials for ultrafast lithium energy storage.
引用
收藏
页码:13419 / 13427
页数:9
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