Lithium-Sulfur is a next generation battery chemistry that offers a theoretical capacity of 1,675 mAh/g, an order of magnitude higher than that of the currently used Li-ion battery cathodes. However, a serious challenge that has plagued the development of this technology is the dissolution and shuttle of intermediate polysulfides (Li 2 S x , x=4-8) in the electrolyte resulting in loss of active material and rapid capacity fade during cycling. I will present two projects from my group both centred around Li-S batteries. In the first part of my talk, I will discuss our work on stabilization of titanium monoxide (TiO) nanoparticles in carbon nanofibers (CNF) through electrospinning and carbothermal processes and their unique bi-functionality – high conductivity and ability to bind polysulfides via Lewis acid-base interactions–as sulfur hosts. The developed 3-D TiO/CNF architecture with the inherent inter-fiber macropores of nanofiber mats provides a much higher surface area (~427 m 2 g -1 ) and overcomes the challenges associated with the use of highly dense powdered Ti-based suboxides/monoxide materials, thereby allowing for high active sulfur loading among other benefits. The developed TiO/CNF-S cathodes exhibit high initial discharge capacities of ~1080 mAh g -1 , ~975 mAh g -1 , and ~791 mAh g -1 at 0.1C, 0.2C, and 0.5C rates, respectively with long-term cycling. Furthermore, free-standing TiO/CNF-S cathodes developed with rapid sulfur melt infiltration (~5 sec) eradicate the need of inactive elements viz. binders, additional current collectors (Al-foil) and additives. Using postmortem XPS and Raman analysis, this study reveals the presence of strong Lewis acid-base interaction between TiO (3d 2 ) and S x 2- through the coordinate covalent Ti-S bond formation. In the second part, I will discuss our work on in-situ infrared spectroelectrochemistry to understand redox mechanisms – a critical step for rational design of cathode systems for Li-S batteries. Specifically, I will discuss the use of sulfur-rich copolymers as active cathode materials and demonstrate in-situ FTIR with attenuated total reflection (ATR) to monitor polysulfide (PS) speciation (S x 2- , 2 ≤ x ≤ 8) and polymeric signature evolution while simultaneously discharging/charging a full battery coin cell.
Xiangwu ZhangLiwen JiOzan ToprakçıYinzheng LiangMataz Alcoutlabi
Min LiuNanping DengJingge JuLanlan FanLiyuan WangZongjie LiHuijuan ZhaoGuang YangWeimin KangJing YanBowen Cheng
M. SivakumarR. SubadeviK. Krishnaveni
Florian NitzeKjell FossumSimon AnderssonShizhao XiongAnders E. C. PalmqvistAleksandar Matic
Ting WuLihong YuNarui LiJingyu Xi