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Effect of electrochemical cycling on microstructure of sulfur electrodes

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dc.contributor.author Yermukhambetova, Assiya
dc.contributor.author Berkinova, Zhazira
dc.contributor.author Golman, Boris
dc.date.accessioned 2018-09-04T04:38:57Z
dc.date.available 2018-09-04T04:38:57Z
dc.date.issued 2018-08-08
dc.identifier.citation Yermukhambetova, Assiya, Berkinova, Zhazira, Golman, Boris. (2018) Effect of electrochemical cycling on microstructure of sulfur electrodes. The 6th International Conference on Nanomaterials and Advanced Energy Storage Systems. Institute of Batteries LLP, Nazarbayev University, and PI “National Laboratory Astana”. p27. en_US
dc.identifier.uri http://nur.nu.edu.kz/handle/123456789/3433
dc.description.abstract In lithium–sulfur (Li–S) batteries, during discharge, there is a significant morphology change as solid sulfur (S) gets dissolved and undergoes successive reduction and finally precipitates as lithium sulfide (Li2S) in porous cathode [1]. This also leads to volume change of the electrolyte in the pore space attributed to precipitation/dissolution of the solid sulfur phase. Moreover, due to the changes in the pore volume coming from the hydrostatic pressure induced by the electrolyte, the cathode microstructure shrinks or swells to accommodate these changes [2]. This leads to mechanical degradation of the electrode over cycling. Thus, the electrochemical performance of lithium sulfur battery is strongly affected by the microstructure of S electrode. en_US
dc.language.iso en en_US
dc.publisher The 6th International Conference on Nanomaterials and Advanced Energy Storage Systems. Institute of Batteries LLP, Nazarbayev University, and PI “National Laboratory Astana”. en_US
dc.rights Attribution-NonCommercial-ShareAlike 3.0 United States *
dc.rights.uri http://creativecommons.org/licenses/by-nc-sa/3.0/us/ *
dc.subject lithium sulfide (Li2S) en_US
dc.subject sulfur (S) en_US
dc.title Effect of electrochemical cycling on microstructure of sulfur electrodes en_US
dc.type Abstract en_US
workflow.import.source science


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