Unsaturation degree of Fe single atom site manipulates polysulfide behavior in sodium-sulfur batteries

Wanqing Song, Zhenzhuang Wen, Xin Wang, Kunyan Qian, Tao Zhang, Haozhi Wang, Jia Ding () and Wenbin Hu
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Wanqing Song: Tianjin University
Zhenzhuang Wen: Tianjin University
Xin Wang: Tianjin University
Kunyan Qian: Tianjin University
Tao Zhang: Tianjin University
Haozhi Wang: Tianjin University
Jia Ding: Tianjin University
Wenbin Hu: Tianjin University

Nature Communications, 2025, vol. 16, issue 1, 1-14

Abstract: Abstract Sodium | |sulfur batteries hold great promise for grid-scale energy storage, yet their performance is hindered by the shuttling and sluggish redox of sulfur species. Herein, we report a strategic design of sulfur hosts modified with coordinatively unsaturated iron single-atom (Fe‒Nx) for sodium | |sulfur batteries. Utilizing theoretical calculations, geometric descriptor γ (lNa‒S/lFe‒N) and electronic descriptor φ (eg /t2g) simultaneously correlated with the unsaturation degree of Fe‒Nx site are proposed. A negative correlation between γ and the adsorption strength of sodium polysulfides, along with a positive correlation between φ and the decomposition capability of Na2S are established. The Fe‒N1 sites, with the minimum γ and maximum φ values, are identified as the optimal functional species for optimizing polysulfides behaviors. Sodium | |sulfur batteries utilizing Fe‒N1 /S positive electrodes deliver improved sulfur utilization (81.4% at 167.5 mA g‒1), sustained rate performance (1003.0 mAh g‒1 at 1675 mA g‒1), and stable cycling (83.5% retention over 450 cycles at 3350 mA g‒1). Moreover, Fe‒N1/S positive electrodes enable sodium | |sulfur pouch cells to deliver a sulfur utilization of 77.4% (1296.9 mAh g‒1) at 0.1 A g‒1. Our work offers a strategy for designing high-activity, fast redox sulfur positive electrodes and validates the practical potential of sodium | |sulfur batteries.

Date: 2025
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DOI: 10.1038/s41467-025-58114-9

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