Iodine-doped sulfurized polyacrylonitrile with enhanced electrochemical performance for lithium sulfur batteries in carbonate electrolyte

• Published in: Chemical engineering journal (Lausanne, Switzerland : 1996) Switzerland : 1996), 2021-08, Vol.418, p.129410, Article 129410
• Main Authors: Ma, Shaobo, Zhang, Zhiguo, Wang, Yang, Yu, Zhenjiang, Cui, Can, He, Mengxue, Huo, Hua, Yin, Geping, Zuo, Pengjian
• Format: Article
• Language: English
• Subjects: Cathode electrolyte interface; Double bond storage lithium; Iodine-doped sulfurized polyacrylonitrile; Lithium sulfur batteries; Solid state NMR
• ISSN: 1385-8947; 1873-3212
• DOI: 10.1016/j.cej.2021.129410

[Display omitted] •The I-S@pPAN was synthesized by a simple co-heating method.•The I-S@pPAN possesses enhanced electronic and ionic conductivity.•The CEI layer containing LiF/LiI can effectively enhance reaction kinetics.•Both -Sx- and double bonds can react with Li+ to provide capacity. Sulfurized polyacrylonitrile (S@pPAN), as a promising high-capacity cathode material, can completely solve the shuttling effect of lithium polysulfide and deliver reliable electrochemical performance in ester-based electrolyte. Until now, the inferior sulfur content, sluggish reaction kinetics and obscure reaction mechanism of the S@pPAN cathodes are still the critical hurdles for attaining their practical application. Herein, the iodine-doped sulfurized polyacrylonitrile (I-S@pPAN) prepared by a simple co-heating method exhibits good electrochemical performance in ester electrolyte. The electrochemical measurements and DFT calculation demonstrate that iodine-doping can effectively promote the electron and Li+ migration of S@pPAN. In-situ EIS spectra reveals the generated cathode electrolyte interface (CEI) layer, containing LiF and LiI, is beneficial to enhance the reaction kinetics. Ex-situ solid state NMR and XPS results demonstrate both -Sx- short-chain oligomers and double bonds (such as CN) in the composites can react with Li+ ions to provide capacity. The I-S@pPAN delivers a high reversible capacity of 1267 mAh g−1 and good capacity retention of 85% after 1000 cycles at 2C. At a high C-rate of 8C (20.35 mA), the I-S@pPAN still achieves a reversible capacity of 1085 and 792 mAh g−1 after 300 cycles. The proposed simple iodine-doping modification method and exploration of reaction mechanism may facilitate the practical application of S@pPAN cathodes.