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Shows enhanced sodium polysulfide conversion in sodium-sulfur batteries, indicating improved efficiency.
Room-temperature sodium–sulfur batteries are practically restricted by the polysulfide shuttle effect, which requires cathode hosts that combine effective physical confinement and chemical catalytic activity. Herein, we develop a Ce-doped hierarchical nanoporous carbon (Ce-MPC) host that integrates physical confinement with tailored interfacial chemistry. The highly dispersed Ce species serve dual functions: strong chemisorption of polysulfides and accelerated catalytic conversion of soluble long-chain sodium polysulfides into insoluble short-chain Na2S2/Na2S. These nanoscale design elements work synergistically to suppress the polysulfide shuttle. As a result, the Ce-MPC@S cathode delivers a specific capacity of 811 mA h g–1 at 0.1 A g–1 after 100 cycles, and an ultralong-life of 1000 cycles with a capacity retention of 367 mA h g–1 at 2.0 A g–1. This work highlights the crucial surface chemistry kinetics coupling for high-performance RT Na–S batteries.
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Ma et al. (2026) studied this question.
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