An in situ confinement strategy to porous poly(3, 4-ethylenedioxythiophene)/sulfur composites for lithium–sulfur batteries. Issue 53 (16th May 2016)

• Record Type: Journal Article
• Authors: Ding, Bing; Chang, Zhi; Wang, Jie; Dou, Hui; Zhang, Xiaogang
• Is Part Of: RSC advances. Volume 6:Issue 53(2016)
• Page Start: 47858
• Page End: 47863
• Publication Date: 2016-05-16
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/c6ra08104e
• Languages: English
• ISSNs: 2046-2069

Abstract

Abstract : Porous poly(3, 4-ethylenedioxythiophene)/sulfur composite was prepared through in situ autocatalytic polymerization of dibromized 3, 4-ethylenedioxythiophene for lithium–sulfur batteries. Abstract : Lithium–sulfur (Li–S) batteries are receiving intense interest because of their high theoretical energy density and low cost. However, the rapid capacity fading is a significant problem facing the application of Li–S batteries. Herein, we describe an in situ confinement strategy for preparing a porous poly(3, 4-ethylenedioxythiophene)/sulfur (pPEDOT/S) composite for Li–S batteries. The as-prepared pPEDOT/S composite exhibits a monodispersed nanostructure with sizes in the range of 400–600 nm. The pPEDOT/S composite electrode exhibits excellent cycling stability and high specific capacity. At a current rate of 0.5C, the pPEDOT/S electrode exhibits a high specific capacity of 883 mA h g −1 and a capacity retention of 71% after 200 cycles. During the charge/discharge process, the porous nanostructure could facilitate rapid electrolyte diffusion and accommodate the volumetric expansion. The chemical interaction between the PEDOT and polysulfides and discharged products could efficiently avoid the dissolution of polysulfides and the irreversible deposition of discharged products. The unique nanostructure plus the excellent electrochemical performances of the composites described in the current study allow for new opportunities to design high-performance electrodes for Li–S batteries.