Iron single-atom catalyst anchored on nitrogen-rich MOF-derived carbon nanocage to accelerate polysulfide redox conversion for lithium sulfur batteries. Issue 6 (28th January 2020)

• Record Type: Journal Article
• Authors: Wang, Cunguo; Song, Hewei; Yu, Congcong; Ullah, Zaka; Guan, Zhixing; Chu, Rongrong; Zhang, Yingfei; Zhao, Liyi; Li, Qi; Liu, Liwei
• Is Part Of: Journal of materials chemistry. Volume 8:Issue 6(2020)
• Page Start: 3421
• Page End: 3430
• Publication Date: 2020-01-28
• Subjects: Materials -- Research -- Periodicals; Chemistry, Analytic -- Periodicals; Environmental sciences -- Research -- Periodicals; 543.0284
• DOI: 10.1039/c9ta11680j
• Languages: English
• ISSNs: 2050-7488

Abstract

Abstract : Permanent adsorption-conversion of lithium polysulfides by iron single atom anchored porous nitrogen-rich carbon nanocages endows lithium sulfur batteries with long lasting rate performance. Abstract : Lithium sulfur batteries (LSBs) have been strongly considered the most promising candidate for next-generation energy storage devices owing to their higher energy density. However, the dissolution of lithium polysulfides (LiPSs) and sluggish conversion kinetics during charge/discharge cycling impede the LSBs. Herein, we employed the nanocage-like nitrogen-rich metal organic framework (MOF)-derived carbon decorated with an iron single-atom (FeSA–CN) catalyst to trigger the surface-mediated reaction of LiPSs. The synergistic effect from the iron single atom (FeSA) and nitrogen-rich porous carbon significantly boost the reaction kinetics and utilization of the sulfur species. The FeSA–CN/S electrode delivered a specific capacity of 1123 mA h g −1 at 0.2C, and exhibited an excellent rate performance of 605 mA h g −1 at 4.0C with an ultralow capacity fading rate of 0.06% per cycle for 500 cycles. This work provides an effective strategy to couple the function of a nanoporous material host and single-atom catalyst for lithium sulfur batteries.