Oxygen Functional Groups Regulating Sulfur Distribution in Carbon Micropores to Enhance Solid-Phase Conversion Reactions for Lithium–Sulfur Batteries

The performance of lithium–sulfur (Li–S) batteries is determined by the cathode, which is to a large extent affected by the low electrical conductivity of S and the dissolution of lithium polysulfides (Li 2 S x ). The confinement of S within microporous C is a promising method to address these challenges. The introduction of O-containing functional groups inside the C micropores improves the capacity for solid-phase conversion in Li–S batteries. However, the mechanism behind this enhanced performance, particularly the role of the O-containing functional groups on S inside the pores, remains unclear. In this study, we investigate the effect of these functional groups on S and/or the Li 2 S x inside the C micropores, focusing on their impact on the electrochemical efficiency and the suppression of polysulfide migration. Electrochemical impedance spectroscopy measurements show that these O-containing functional groups accelerate charge transfer reactions and Li + ion diffusion. Cross-sectional scanning transmission electron microscopy-electron energy loss spectroscopy of the S–C composites reveals that, without O-containing functional groups, S and/or Li 2 S x migrate and localize to the inner edge of the carbon host during cycling. In contrast, the presence of O-containing functional groups inside the pores of the microporous C host maintains a uniform distribution of S and/or Li 2 S x within the C micropores, explaining the improved solid-phase conversion performance in Li–S batteries. In conclusion, this paper proposes a new design for the cathode of high-performance Li–S batteries. For the first time, experimental evidence is provided to confirm the mechanism whereby the introduction of O-containing functional groups into microporous C enhances the performance of Li–S batteries by lowering the resistance and preventing Li 2 S x migration. These modifications improve the electrochemical efficiency and offer insights for developing more effective cathodes to advance the commercialization of Li–S batteries.