| Literature DB >> 25969951 |
Bing Ding1, Zhi Chang1, Guiyin Xu1, Ping Nie1, Jie Wang1, Jin Pan1, Hui Dou1, Xiaogang Zhang1.
Abstract
Given their high theoretical energy density, lithium-sulfur (Li-S) batteries have recently attracted ever-increasing research interest. However, the dissolution of polysulfides and uncontrolled deposition of insoluble discharge product significantly hinder the cycling stability. Herein, a nanospace-confinement copolymerization strategy for encapsulating polymeric sulfur into porous carbon matrix is presented. The morphologies and sulfur contents of carbon/polymeric sulfur (C/PS) composites could be readily tailored by controlling the copolymerization time. Confining polymeric sulfur in the porous carbon with abundant interparticle pores facilitates rapid electronic/ionic transport and mitigates dissolution of polysulfides intermediates. More importantly, the organic sulfur units dispersed in the insoluble/insulating Li2S2/Li2S phase could prevent its irreversible deposition. Such nanostructure with tailored chemistry property permits the C/PS electrodes to exhibit enhanced cycling stability and high rate capability. The nanospace-confinement copolymerization strategy features general and facial advantages, which may provide new opportunities for the future development of advanced sulfur cathodes.Entities:
Keywords: carbon/polymeric sulfur composites; copolymerization; electrochemistry; lithium−sulfur batteries; nanospace-confinement
Year: 2015 PMID: 25969951 DOI: 10.1021/acsami.5b00870
Source DB: PubMed Journal: ACS Appl Mater Interfaces ISSN: 1944-8244 Impact factor: 9.229