Accelerated polysulfide conversion on hierarchical porous vanadium–nitrogen–carbon for advanced lithium–sulfur batteries. Issue 2 (17th December 2019)

• Record Type: Journal Article
• Authors: Fan, Yining; Ma, Feng; Liang, Jiashun; Chen, Xian; Miao, Zhengpei; Duan, Shuo; Wang, Liang; Wang, Tanyuan; Han, Jiantao; Cao, Ruiguo; Jiao, Shuhong; Li, Qing
• Is Part Of: Nanoscale. Volume 12:Issue 2(2020)
• Page Start: 584
• Page End: 590
• Publication Date: 2019-12-17
• Subjects: Nanoscience -- Periodicals; Nanotechnology -- Periodicals; 620.505
• DOI: 10.1039/c9nr09037a
• Languages: English
• ISSNs: 2040-3364

Abstract

Abstract : Hierarchical porous V–N–C with V–N x sites demonstrates enhanced catalytic activity for polysulfide conversion, and thus shows excellent performance in Li–S batteries. Abstract : With high theoretical specific density, low cost, and non-toxicity, Li–S batteries are regarded as a promising candidate for next-generation energy storage systems. However, the shuttling of soluble Li polysulfides (LiPSs) results in self-discharge and rapid capacity degradation. Herein, nitrogen-doped hierarchical porous carbon with embedded highly dispersed vanadium (v )–N x sites (V–N–C) is developed as a high-performance Li–S battery cathode for the first time. The metal–organic polymer supramolecule structure formed by the electrostatic/hydrogen bond interaction of chitosan–VO3 − strongly stabilizes V to generate a high density of V–N x /C sites. During the discharge/charge process, the unique V–N x /C active sites can serve as efficient catalysts to accelerate the redox kinetics of LiPSs, while the hierarchical porous carbon structure of V–N–C benefits the diffusion/transfer of Li + /e − and suppresses the shuttling of LiPSs. As a result, the S/V–N–C composite delivers a high specific capacity of 1111.2 mA h g −1 at 0.5C and maintains 573.6 mA h g −1 at 5C with a low capacity decay rate of 0.087% per cycle (over 500 cycles at 1C). The rate performance of the developed V–N–C cathode in Li–S batteries is superior to that of most of the reported M–N–C and carbon material/metal compound composite electrodes.