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Prevention of sulfur diffusion using MoS2-intercalated 3D-nanostructured graphite for high-performance lithium-ion batteries. | LitMetric

Prevention of sulfur diffusion using MoS2-intercalated 3D-nanostructured graphite for high-performance lithium-ion batteries.

Nanoscale

Centre for Integrated Nanostructure Physics (CINAP), Institute of Basic Science (IBS), Department of Chemistry, Sungkyunkwan University, 300 Cheoncheon-Dong, Jangan-Gu, Suwon, Gyeonggi-Do 440-746, South Korea.

Published: July 2015

We report new three-dimensional (3D)-nanostructured MoS2-carbonaceous materials in which MoS2 sheets are intercalated between the graphite layers that possess a multiply repeated graphite/MoS2/graphite structure which prevents the aggregation of MoS2 and diffusion of sulfur from carbonaceous materials, enhancing the cycling stability of Li-ion batteries. We developed an efficient and scalable process applicable to mass production for synthesizing non-aggregated MoS2-intercalated 3D hybrid-nanostructured graphite based on stress induced and microwave irradiation. X-ray diffraction, X-ray photospectroscopy, Raman spectroscopy, field emission scanning electron microscopy, and high-resolution transmission electron microscopy analyses demonstrated that the as-synthesized materials consisted of MoS2-intercalated 3D hybrid-nanostructured graphite platelets that had a multiply repeated graphite/MoS2/graphite structure. The obtained MoS2-graphite powder surpasses MoS2 as an anode material in terms of specific capacity, cyclic stability, and rate performances at high current densities for Li-ion batteries. The electrochemical impedance spectroscopy demonstrated that the graphite sheets not only reduced the contact resistance in the electrode but also facilitated electron transfer in the lithiation/delithiation processes. The superior electrochemical performances especially for the cycling stability of the Li-ion battery originate from prevention of the sulfur diffusion of the MoS2-intercalated 3D-nanostructured graphite.

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Source
http://dx.doi.org/10.1039/c5nr03111gDOI Listing

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