Managing the redox reactions of polysulfides is crucial for improving the performance of lithium-sulfur batteries (LSBs). Herein, we introduce a progressive theoretical framework: the balanced d-band model, which is based on classical d-band center theory. Specifically, by optimizing the position of the d-band center in the middle between the highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) of each sulfur species, balanced and fast oxidation and reduction reactions of the sulfur species can be achieved simultaneously. To validate this theory, we synthesized a catalyst featuring an in situ phosphorized heterostructure (NOP) based on nickel oxide (NiO), which effectively optimizes the d-band center at the middle between the HOMO and LUMO of each sulfur species. Aided by the balanced oxidation and reduction kinetics of the sulfur species, the NOP-based cell achieved a high reversible capacity, superior cycling stability, and prolonged cycle life. This study extends the conventional d-band center theory and introduces an innovative theoretical model to expand our understanding of the internal reaction mechanisms in LSBs.
Keywords: adsorption-catalysis-desorption; bifunctional host; d-band center; practical Li−S batteries; sulfur species oxidation.