RESUMEN
Exploring advanced sulfur cathode materials with high catalytic activity to accelerate the slow redox reactions of lithium polysulfides (LiPSs) is of great significance for lithium-sulfur batteries (LSBs). In this study, a coral-like hybrid composed of cobalt nanoparticle-embedded N-doped carbon nanotubes supported by Vanadium (III) oxide (V2O3) nanorods (Co-CNTs/C @V2O3) was designed as an efficient sulfur host using a simple annealing process. Characterization combined with electrochemical analysis confirmed that the V2O3 nanorods exhibited enhanced LiPSs adsorption capacity, and the in situ grown short-length Co-CNTs improved electron/mass transport and enhanced the catalytic activity for conversion to LiPSs. Owing to these merits, the S@Co-CNTs/C@V2O3 cathode exhibits effective capacity and cycle lifetime. Its initial capacity was 864 mAh g-1 at 1.0C and remained at 594 mAh g-1 after 800cycles with a decay rate of 0.039%. Furthermore, even at a high sulfur loading (4.5 mg cm-2), S@Co-CNTs/C@V2O3 also shows acceptable initial capacity of 880 mAh g-1 at 0.5C. This study provides new ideas for preparing long-cycle S-hosting cathodes for LSBs.
RESUMEN
Accelerating phase transposition efficiency of lithium polysulfides (LiPSs) to L2S and hampering the solution of LiPSs are the keys to stabilizing lithium-sulfur (Li-S) batteries. Hence, the sulfiphilic ultrafine Co9S8 nanoparticles embedded lithiophilic N, S co-doping carbon nanofibers (Co9S8/NSCNF) are prepared via the dual-template method, which are then used as sulfur host in Li-S batteries. Particularly, the double active sites (Co9S8 and N, S) in Co9S8/NSCNF are prone to form "Co-S", "Li-O" or "Li-N" bonds, and then simultaneously improving the chemisorption and interface transposition capability of LiPSs. In case of the S@ Co9S8/NSCNF composites with high sulfur loading of 89% are employed as cathode, the cell possesses optimized "sulfiphilicity" and "lithiophilicity", which achieves remarkable sulfur electrochemistry, including outstanding reversibility of 816.8mAhg-1 over 500 cycles at 1.0C, excellent rate property of 742.2mAhg-1at 5.0C, and long-term cycling with a low attenuation of 0.011% per cycle over 1800 cycles at 3.0C. Impressively, a remarkable areal capacity of 11.51mAhcm-2 is retained under the sulfur loading of 15.3 mg cm-2 for 50 cycles. This research will deepen the understanding of the complex LiPSs interface transposition procedure and provide new ideas for the design of new host materials.