Single step transformation of sulphur to Li2S2/Li2S in Li-S batteries

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作者
M. Helen
M. Anji Reddy
Thomas Diemant
Ute Golla-Schindler
R. Jürgen Behm
Ute Kaiser
Maximilian Fichtner
机构
[1] Helmholtz Institute Ulm (HIU),Electron Microscopy Group of Materials Science
[2] Institute of Surface Chemistry and Catalysis,undefined
[3] Ulm University,undefined
[4] Central Facility for Electron Microscopy,undefined
[5] Ulm University,undefined
[6] Institute of Nanotechnology,undefined
[7] Karlsruhe Institute of Technology,undefined
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摘要
Lithium-sulphur batteries have generated tremendous research interest due to their high theoretical energy density and potential cost-effectiveness. The commercial realization of Li-S batteries is still hampered by reduced cycle life associated with the formation of electrolyte soluble higher-order polysulphide (Li2Sx, x = 4–8) intermediates, leading to capacity fading, self-discharge and a multistep voltage profile. Herein, we have realized a practical approach towards a direct transformation of sulphur to Li2S2/Li2S in lithium-sulphur batteries by alteration of the reaction pathway. A coconut shell derived ultramicroporous carbon-sulphur composite cathode has been used as reaction directing template for the sulphur. The lithiation/delithiation and capacity fading mechanism of microporous carbon confined sulphur composite was revealed by analyzing the subsurface using X-ray photoelectron spectroscopy. No higher-order polysulphides were detected in the electrolyte, on the surface and in the subsurface of the cathode composite. The altered reaction pathway is reflected by a single-step profile in the discharge/charge of a lithium-sulphur cell.
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