4.6 Article

Kinetics of sulphur dissolution in lithium-sulphur batteries

期刊

JOURNAL OF PHYSICS-ENERGY
卷 4, 期 2, 页码 -

出版社

IOP Publishing Ltd
DOI: 10.1088/2515-7655/ac521d

关键词

sulphur; dissolution; DOL; DME electrolyte; diffusion; Li-S batteries

资金

  1. University of Surrey, Faraday Institute in association with the LiSTAR project [FIRG014]
  2. EPSRC via the CoA grant in association with the HiPoBat project

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This study investigates the dissolution kinetics of solid sulphur in DOL:DME solution and presents a novel model for sulphur dissolution and electrolyte impregnation. The results show that solid sulphur has fast dissolution kinetics at 20°C but low solubility, which limits its dissolution. In addition, swelling of the solid sulphur region was observed and the diffusion coefficient of the DOL:DME solution in the solid sulphur was determined.
This study investigates and determines the dissolution kinetics of solid sulphur in DOL:DME solution, a typical electrolyte solution for lithium-sulphur (Li-S) batteries, at four different temperatures, in the range of 17 degrees C-20 degrees C. The dissolution kinetics is considered as a function of the solid sulphur-solution interfacial area. The analysis yielded fast dissolution kinetics with a mass transfer coefficient of 2.3 x 10(-3) m s(-1) at 20 degrees C but low sulphur solubility of 0.058 S mol lt(-1), with the latter being a limiting factor in sulphur dissolution. In later stages, swelling of the solid sulphur region was also observed as a function of time from which the diffusion coefficient of the DOL:DME solution in the solid sulphur was determined. A novel model for the sulphur dissolution and electrolyte impregnation in a Li-S cathode in battery fabrication is presented taking into account the pore size distribution of the cathode host. A computer simulation was carried out and the model and the dissolution parameter values were validated by comparing the predictions with experimental data from in operando microscopy during the dissolution of sulphur and infiltration of the DOL:DME solution in a commercial sulphur-conductive carbon cathode.

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