In Situ Observation of Na<sub>2</sub>S Growth: A Step Toward High-Energy and Safer Room Temperature Sodium Sulfur Batteries.

Xiong, Zhen; Chen, Si; Guo, Jinqing; Cheng, Ningyan; Zhang, Shilin; Zhang, Binwei; Wei, Zidong; Sun, Shigang et al. · Adv Mater · 2026

basic_science · Level V

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Abstract

The Na<sub>2</sub>S cathode presents a promising metal-free sodium configuration for high-energy room-temperature sodium sulfur (RT Na─S) batteries. However, the rational design of Na<sub>2</sub>S cathodes to overcome their poor electronic conductivity and sluggish conversion kinetics remains a major challenge. Here, an in situ carbothermic reduction strategy is reported to fabricate atomic Mo anchored on Na<sub>2</sub>S/C (including single Mo atom and Mo clusters) as cathode materials for RT Na─S batteries. In situ transmission electron microscopy and X-ray diffraction technique reveal that atomic Mo could form a low-temperature eutectic phase, which catalytically lowers the formation temperature of Na<sub>2</sub>S. This Mo-Na<sub>2</sub>S/C exhibits remarkable cyclic stability, achieving an initial capacity of 1617 mAh g<sup>-1</sup> at 0.1 A g<sup>-1</sup> and a low activation voltage of 1.89 V. Notably, when paired with hard carbon, the safe sodium full cell delivers an impressive initial reversible capacity of 952 mAh g<sup>-1</sup>. Experimental results and theoretical calculations reveal that the atomic Mo facilitates the interfacial electron transfer between Mo and Na<sub>2</sub>S, which modulates the bandgap of Na<sub>2</sub>S and reduces its reaction barriers to polysulfide, thereby enhancing the reaction kinetics. These findings offer an effective strategy for developing high-performance Na<sub>2</sub>S cathodes and provide deeper insights into electrode preparation mechanisms.