Suppressing the polysulfide shuttle effect and accelerating the sulfur redox kinetics remain pivotal challenges for advancing the practical viability of lithium–sulfur batteries (LSBs). In this study, an iodine-doped carbon nitride (I-CN) material was synthesized via a one-step annealing strategy and employed as a metal-free sulfur cathode host. Compared to its pristine counterpart, I-CN exhibits a substantially increased specific surface area, which facilitates the homogeneous dispersion of sulfur species. More importantly, the incorporation of iodine atoms disrupts the equilibrium of the electron cloud distribution within the CN framework, leading to enhanced electron delocalization. This electronic modulation not only significantly improves the charge transport properties of carbon nitride but also strengthens the adsorption of lithium polysulfides (LiPS) and promotes Li2S nucleation, thereby enabling fast and durable sulfur redox reactions. Benefiting from these synergistic effects, the S@I-CN electrode achieves high sulfur utilization, delivering an initial discharge capacity of 1341.9 mAh g−1 at 0.1C. Even at a high current density of 5C, a remarkable reversible capacity of 472.7 mAh g−1 is retained. Notably, the electrode retains 66.2% of its initial capacity after 800 cycles, demonstrating excellent long-term cycling stability. This halogen-based heteroatom doping strategy thus not only enhances the electrochemical performance of carbon nitride materials in LSBs through the rational manipulation of electron delocalization, but also offers a promising direction for the design of novel metal-free electrocatalysts in related energy conversion systems.
Yan et al. (Wed,) studied this question.