4.7 Article

Templated spherical coassembly strategy to fabricate MoS2/C hollow spheres with physical/chemical polysulfides trapping for lithium-sulfur batteries

Journal

JOURNAL OF MATERIALS SCIENCE & TECHNOLOGY
Volume 98, Issue -, Pages 136-142

Publisher

JOURNAL MATER SCI TECHNOL
DOI: 10.1016/j.jmst.2021.05.022

Keywords

Lithium-sulfur batteries; Cathode; MoS2; C hollow spheres; Physical confinement; Chemical adsorption

Funding

  1. National Natural Science Foundation [51972235]
  2. China Postdoctoral Science Foundation [2020M680538]
  3. Natural Science Foundation of Shanghai [17ZR1447800]
  4. Jiangsu Key RD Plan [BE2018006-4]
  5. Program for Professor of Special Appointment (Eastern Scholar) at Shanghai Institutions of Higher Learning
  6. Fundamental Research Funds for the Central Universities

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The MoS2/C hollow spheres fabricated via a novel templated spherical coassembly strategy demonstrate excellent performance as a sulfur host material, with advantages including maximizing sulfur utilization, suppressing electrolyte shuttling effect, improving ionic transport, cycling stability, and rate capability.
Rational design of advanced polar hosts with high sulfur loading, facilitated ionic/electronic transport and effectively suppressed shuttling effect has great potential for high performance lithium-sulfur batteries, yet it remains challenging. Here we propose a novel templated spherical coassembly strategy to fabricate the MoS 2 /C hollow spheres as an efficient sulfur host material. The unique hollow structure provides enough interior space for accommodating a substantial amount of sulfur, and effectively suppresses the diffusion of dissolved polysulfides by both physical confinement and chemical adsorption. Moreover, the ionic transport as well as the ability to mitigate volume variation upon cycling is also improved, thereby maximizing the utilization of sulfur. Owing to these merits, when evaluated as a sulfur host for lithiumsulfur batteries, the MoS 2 /C hollow spheres exhibit appealing electrochemical performance with an impressive specific capacity of 1082 mA h g -1 at 0.1 C, excellent rate capability and superior cycling stability with a low fading rate of 0.04% per cycle. (c) 2022 Published by Elsevier Ltd on behalf of The editorial office of Journal of Materials Science & Technology.

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