Enhanced Cycling Stability of Lithium–Sulfur batteries by Electrostatic-Interaction. (10th November 2015)

• Record Type: Journal Article
• Authors: Ma, Zhaoling; Huang, Xiaobing; Jiang, Qianqian; Huo, Jia; Wang, Shuangyin
• Is Part Of: Electrochimica acta. Volume 182(2015)
• Page Start: 884
• Page End: 890
• Publication Date: 2015-11-10
• Subjects: poly(diallyl dimethylammonium) chloride -- electrostatic interaction -- cycling stability -- grapheme -- Lithium-sulfur batteries; Electrochemistry -- Periodicals; Electrochemistry, Industrial -- Periodicals; 541.37
• DOI: 10.1016/j.electacta.2015.10.009
• Languages: English
• ISSNs: 0013-4686

Abstract

Graphical abstract: Highlights: Electrostatic interaction is utilized to hinder the shuttling of polysulfides. Directly functionalizing SG can better prolong the cycle life of Li–S batteries. SG/PDDA showed significantly improved capacity retention. Abstract: Lithiums–sulfur battery is considered as one of the most promising energy storage devices to replace the current Li ion batteries because of its high theoretical capacity of 1675 mA h g −1 . However, the poor cycle stability hinders the further development of this battery system. In order to improve the stability of Li–S batteries, the diffusion of polysulfides from electrodes into electrolyte should be suppressed. Herein, we utilize a positively charged polyelectrolyte to functionalize the electrode materials with the aim to hamper the polysulfides dissolution via electrostatic interaction between strong positively charged polyelectrolyte and negatively charged polysulfides anion. The effect of the functionalization quantity of poly(diallyl dimethylammonium) chloride (PDDA) and functionalization sequence on cycling performances is investigated in detail. It is found that the sulfur–graphene composite (SG) directly functionalized with 10 times PDDA exhibited best cycling stability. At a discharge current density of 0.2 C, much higher capacity retention was realized on the functionalized electrodes than the unfunctionalized (81% vs. 47.3%) after 120 cycles. The as-observed results demonstrate that the electrostatic interaction can effectively prolong the cycling life of Li–S batteries, which provides a new promising strategy for improving the electrochemical performance of Li–S batteries.