A spatial confiment of polysulfides using the metal compound additives having polar surfaces has been considered to be a promising approach to address the insufficient rate capability and cyclability of lithium–sulfur batteries. Herein, we report a more effective approach outperforming this conventional one: a heterogeneous catalysis to promote polysulfide fragmentations. It was revealed using combined computational and experimental approaches that an ultrastrong adsorption of elemental sulfur on TiN surfaces resulted in a spontaenous fragmentation into shorter chains of polysulfides. This heterogeneous catalysis reaction improved the sluggish kinetics of polysulfide reduction because of the chemical disproportionation at the second plateau. A markedly enhanced rate capability was finally obtained, exhibiting a discharge capacity of 700 mAh g –1 at a scan rate of 5C.
No takes yet. Share an insight, caveat, or question.
Jeong et al. (2017) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: