He Xuanmeng, Li Beijun, Lei Zehua, Liu Hui, Wang Shaolan, Qiao Tong, Feng Yanqi, Wang Xinzhen
School of Materials Science and Engineering, Shaanxi Key Laboratory of Green Preparation and Functionalization for Inorganic Materials, Shaanxi University of Science and Technology, Xi'an, Shaanxi 710021, PR China.
School of Materials Science and Engineering, Shaanxi Key Laboratory of Green Preparation and Functionalization for Inorganic Materials, Shaanxi University of Science and Technology, Xi'an, Shaanxi 710021, PR China.
J Colloid Interface Sci. 2022 Nov 15;626:963-974. doi: 10.1016/j.jcis.2022.07.015. Epub 2022 Jul 5.
The poor conductivity of sulfur, the shuttle effect and sluggish redox reaction kinetics of lithium polysulfides (LiPSs) are considered the main obstacles to the practical application of Lithium-sulfur (Li-S) batteries. Thus, it is urgent to design multifunctional host materials to eliminate these obstacles. Herein, we designed a hollow flower-like CoTiO wrapped by reduced graphene oxide (h-CoTiO@rGO) as sulfur host materials. The hollow structure of h-CoTiO@rGO not only endows sufficient space for high sulfur loading, but also physically and chemically confines the shuttle effect of LiPSs through the formation of Co-S chemical bonding. The large specific surface area and excellent electrocatalytic ability of h-CoTiO@rGO provide amounts of active sites to accelerate the redox reaction of LiPSs. Meanwhile, the conductive reduced graphene oxide (rGO) covered on the surface of CoTiO microspheres offers an interconnected conductive network to support the fast electron/ion transfer. Profit from these merits, the battery employing the multifunctional h-CoTiO@rGO as sulfur host exhibited excellent cycling stability with an ultralow capacity fading of 0.0127 % per cycle after 500 cycles at 1C. Even the battery with high sulfur loading of 5.2 mg/cm still delivered a high area capacity of 5.02 mAh/cm, which was competitive with the commercial Li-ion batteries. Therefore, the competitive capacity and superior cycling stability suggest that the h-CoTiO@rGO/S cathode is a potential candidate for high-performance Li-S batteries.
硫的低电导率、多硫化锂(LiPSs)的穿梭效应和缓慢的氧化还原反应动力学被认为是锂硫(Li-S)电池实际应用的主要障碍。因此,迫切需要设计多功能主体材料来消除这些障碍。在此,我们设计了一种由还原氧化石墨烯包裹的中空花状CoTiO(h-CoTiO@rGO)作为硫主体材料。h-CoTiO@rGO的中空结构不仅为高硫负载提供了足够的空间,还通过形成Co-S化学键在物理和化学上限制了LiPSs的穿梭效应。h-CoTiO@rGO的大比表面积和优异的电催化能力提供了大量活性位点,以加速LiPSs的氧化还原反应。同时,覆盖在CoTiO微球表面的导电还原氧化石墨烯(rGO)提供了一个相互连接的导电网络,以支持快速的电子/离子传输。得益于这些优点,采用多功能h-CoTiO@rGO作为硫主体的电池表现出优异的循环稳定性,在1C下500次循环后,每循环的超低容量衰减为0.0127%。即使是硫负载量高达5.2 mg/cm²的电池仍能提供5.02 mAh/cm²的高面积容量,这与商业锂离子电池具有竞争力。因此,具有竞争力的容量和优异的循环稳定性表明h-CoTiO@rGO/S正极是高性能Li-S电池的潜在候选材料。