Hollow Defect-Rich Nanofibers as Sulfur Hosts for Lithium-Sulfur Batteries.
Shouyu HongQiang LiJia LiLuqiao JinLingfeng ZhuXiangzeng MengYeqiang CheZhen-Yu YangZe ZhangYu JiJianxin CaiPublished in: ACS applied materials & interfaces (2024)
The slow redox kinetics of lithium-sulfur batteries severely limit their application, and sulfur utilization can be effectively enhanced by designing different cathode sulfur host materials. Herein, we report the hollow porous nanofiber LaNi 0.6 Co 0.4 O 3 as a bidirectional host material for lithium-sulfur batteries. After Co is substituted into LaNiO 3 , oxygen vacancies are generated to enhance the material conductivity and enrich the active sites of the material, and the electrochemical reaction rate can be further accelerated by the synergistic catalytic ability of Ni and Co elements in the B-site of the active site of LaNi 0.6 Co 0.4 O 3 . As illustrated by the kinetic test results, LaNi 0.6 Co 0.4 O 3 effectively accelerated the interconversion of lithium polysulfides, and the nucleation of Li 2 S and the dissolution rate of Li 2 S were significantly enhanced, indicating that LaNi 0.6 Co 0.4 O 3 accelerated the redox kinetics of the lithium-sulfur battery during the charging and discharging process. In the electrochemical performance test, the initial discharge specific capacity of S/LaNi 0.6 Co 0.4 O 3 was 1140.4 mAh g -1 at 0.1 C, and it was able to release a discharge specific capacity of 584.2 mAh g -1 at a rate of 5 C. It also showed excellent cycling ability in the long cycle test, with a single-cycle capacity degradation rate of only 0.08%. Even under the harsh conditions of high loaded sulfur and low electrolyte dosage, S/LaNi 0.6 Co 0.4 O 3 still delivers excellent specific capacity and excellent cycling capability. Therefore, this study provides an idea for the future development of bidirectional high-activity electrocatalysts for lithium-sulfur batteries.