Demonstrates improved lithium transport and stability in polymer frameworks, suggesting advancements in battery technology.
Organic sulfur cathodes for lithium–sulfur (Li–S) batteries hold great promise for suppressing polysulfide shuttling, yet their practical implementation is hindered by sluggish Li + transport kinetics and intricate synthesis processes. Here, we present a catalyst-free solid-state synthesis strategy to construct a sulfur-containing polymer molecular framework (PEI@TPAL@S) by integrating terephthalaldehyde-based motifs (TPAL) and sulfur clusters into a polyethylenimine (PEI) backbone. The designed framework features abundant nitrogen-active sites and hierarchically interconnected nanopores, synergistically enhancing polysulfide confinement and Li + diffusion. The PEI@TPAL@S cathode achieves a sulfur content of 77.0 wt %, a Li + diffusion coefficient 100-fold higher than conventional sulfur-containing polymers and exceptional rate capability (726 mAh g –1 at 5C). Remarkably, it demonstrates ultralong cycling stability with a minimal capacity decay rate of 0.051% per cycle over 500 cycles at 5C. Mechanistic studies reveal that the covalent Li–N bonding and porous architecture facilitate efficient polysulfide adsorption and rapid Li + transport, while density functional theory (DFT) calculations confirm reduced energy barriers for lithium sulfide nucleation. This work provides a scalable pathway for high-performance organic sulfur cathodes and advances the molecular-level design of sulfur-containing polymers for next-generation energy storage systems.
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Lu et al. (2025) studied this question.
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