详细信息
2D Nanospace Confined Synthesis of Pseudocapacitance-Dominated MoS2-in-Ti3C2 Superstructure for Ultrafast and Stable Li/Na-Ion Batteries ( SCI-EXPANDED收录 EI收录)
文献类型:期刊文献
英文题名:2D Nanospace Confined Synthesis of Pseudocapacitance-Dominated MoS2-in-Ti3C2 Superstructure for Ultrafast and Stable Li/Na-Ion Batteries
作者:Ma, Kun[1];Jiang, Hao[1];Hu, Yanjie[1];Li, Chunzhong[1]
机构:[1]East China Univ Sci & Technol, Sch Mat Sci & Engn, Minist Educ, Key Lab Ultrafine Mat, Shanghai 200237, Peoples R China
年份:2018
卷号:28
期号:40
外文期刊名:ADVANCED FUNCTIONAL MATERIALS
收录:;EI(收录号:20183505758959);WOS:【SCI-EXPANDED(收录号:WOS:000446155700026)】;
基金:This work was supported by the National Natural Science Foundation of China (21522602, 51672082, and 91534202), the Shanghai Scientific and Technological Innovation Project (18JC1410500), the Basic Research Program of Shanghai (17JC1402300), the National Program for Support of Top-Notch Young Professionals, the Innovation Program of Shanghai Municipal Education Commission, and the Fundamental Research Funds for the Central Universities (222201718002).
语种:英文
外文关键词:confined synthesis; energy storage; high rate; MoS2 nanocrystals; pseudocapacitance
摘要:Exploring a universal strategy to implement the precise control of 2D nanomaterials in size and layer number is a big challenge for achieving ultrafast and stable Li/Na-ion batteries. Herein, the confined synthesis of 1-3 layered MoS2 nanocrystals into 2D Ti3C2 interlayer nanospace with the help of electrostatic attraction and subsequent cetyltrimethyl ammonium bromide (CTAB) directed growth is reported. The MoS2 nanocrystals are tightly anchored into the interlayer by 2D confinement effect and strong MoC covalent bond. Impressively, the disappearance of Li+ intercalated into MoS2 reduction peak is successfully observed for the first time in the experiment, showing in a typical surface-controlled charge storage behavior. The pseudocapacitance-dominated contribution guarantees a much faster and more stable Li/Na storage performance. As predicted, this electrode exhibits a very high Li+ storage capacity of 340 mAh g(-1) even at 20 A g(-1) and a long cycle life (>1000 times). It also shows an excellent Na+ storage capacity of 310 mAh g(-1) at 1 A g(-1) with a 1600 times high-rate cycling. Such impressive confined synthesis strategy can be extended to the precise control of other 2D nanomaterials.
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