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Rechargeable Lithium Sulfur Battery : I. Structural Change of Sulfur Cathode During Discharge and Charge

Rechargeable Lithium Sulfur Battery : I. Structural Change of Sulfur Cathode During Discharge and... In this paper, the structural change of the sulfur cathode during the electrochemical reaction of a lithium sulfur battery employing 0.5 M -tetra(ethylene glycol) dimethyl ether (TEGDME) was studied by means of scanning electron microscopy (SEM), X-ray diffraction (XRD), and wave dispersive spectroscopy (WDS). The discharge process of the lithium sulfur cell could be divided in the first discharge region (2.4-2.1 V) where the reduction of elemental sulfur to form soluble polysulfides and further reduction of the soluble polysulfide occur, and the second discharge region (2.1-1.5 V) where the soluble polysulfides are reduced to form a nonuniform solid film covered over the carbon matrix. It was also found that the charge of lithium sulfur cell leads to the conversion from to the soluble polysulfide, resulting in the removal of layer formed on carbon matrix. However, the oxidization of the soluble polysulfide to solid sulfur hardly occurs and few are left on carbon matrix even at 100% depth of charge. © 2003 The Electrochemical Society. All rights reserved. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Journal of the Electrochemical Society IOP Publishing

Rechargeable Lithium Sulfur Battery : I. Structural Change of Sulfur Cathode During Discharge and Charge

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References (10)

Copyright
Copyright © 2003 ECS - The Electrochemical Society
ISSN
0013-4651
eISSN
1945-7111
DOI
10.1149/1.1571532
Publisher site
See Article on Publisher Site

Abstract

In this paper, the structural change of the sulfur cathode during the electrochemical reaction of a lithium sulfur battery employing 0.5 M -tetra(ethylene glycol) dimethyl ether (TEGDME) was studied by means of scanning electron microscopy (SEM), X-ray diffraction (XRD), and wave dispersive spectroscopy (WDS). The discharge process of the lithium sulfur cell could be divided in the first discharge region (2.4-2.1 V) where the reduction of elemental sulfur to form soluble polysulfides and further reduction of the soluble polysulfide occur, and the second discharge region (2.1-1.5 V) where the soluble polysulfides are reduced to form a nonuniform solid film covered over the carbon matrix. It was also found that the charge of lithium sulfur cell leads to the conversion from to the soluble polysulfide, resulting in the removal of layer formed on carbon matrix. However, the oxidization of the soluble polysulfide to solid sulfur hardly occurs and few are left on carbon matrix even at 100% depth of charge. © 2003 The Electrochemical Society. All rights reserved.

Journal

Journal of the Electrochemical SocietyIOP Publishing

Published: May 5, 2003

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