Tang Xianyi, Gan Ruiyi, Tan Lianqiao, Tong Cheng, Li Cunpu, Wei Zidong
National-Municipal Joint Engineering Laboratory for Chemical Process Intensification and Reaction, College of Chemistry and Chemical Engineering, Chongqing University, Chongqing 400044, China.
ACS Appl Mater Interfaces. 2021 Nov 24;13(46):55235-55242. doi: 10.1021/acsami.1c17881. Epub 2021 Nov 9.
High theoretical specific capacity and rich resources in nature make sulfur an ideal cathode material for lithium-metal batteries. However, the shuttle effect and sluggish reduction reaction kinetics of lithium polysulfides (LiPSs) seriously affect the performance of the batteries. Here, we report GO-d-TiCT MXene aerogels with a novel three-dimensional (3D) reticular structure that served as sulfur host cathode materials for lithium-sulfur batteries (LiSBs), which benefits adsorption/catalytic conversion of LiPSs simultaneously. The dissolved LiPSs can be rapidly captured through chemisorption and then catalyzed into insoluble LiS by low-coordinated-state Ti on the d-TiCT MXene surface. The combination of adsorption and catalysis enormously improves the capacity and cycling performance of LiSBs. At an S mass loading of 1.5 mg cm, the cell with the S@GM0.4 composite electrode achieves excellent cycling performance. The discharge specific capacity of 1039 mA h g (1.56 mA h cm) decays to 542.9 mA h g after 1000 cycles with a capacity fading rate of 0.048% per cycle at 0.5 C. Even at an S mass loading of 4.88 mg cm, an areal capacity of 4.3 mA h cm can be achieved at 0.2 C.
高理论比容量以及自然界中丰富的资源使硫成为锂金属电池理想的正极材料。然而,多硫化锂(LiPSs)的穿梭效应和缓慢的还原反应动力学严重影响电池性能。在此,我们报道了具有新型三维(3D)网状结构的氧化石墨烯修饰的d-TiCT MXene气凝胶,其作为锂硫电池(LiSBs)的硫主体正极材料,同时有利于LiPSs的吸附/催化转化。溶解的LiPSs可通过化学吸附迅速捕获,然后被d-TiCT MXene表面低配位态的Ti催化转化为不溶性的LiS。吸附与催化的结合极大地提高了LiSBs的容量和循环性能。在硫质量负载为1.5 mg cm时,具有S@GM0.4复合电极的电池表现出优异的循环性能。在0.5 C下,1039 mA h g(1.56 mA h cm)的放电比容量在1000次循环后衰减至542.9 mA h g,容量衰减率为每循环0.048%。即使在硫质量负载为4.88 mg cm时,在0.2 C下仍可实现4.3 mA h cm的面积容量。