材料科学
阴极
共晶体系
化学工程
透射电子显微镜
电极
钠
硫黄
纳米颗粒
原位
纳米技术
电子转移
电导率
锡
原子单位
衍射
Atom(片上系统)
催化作用
阳极
无机化学
金属
动力学
氧化还原
作者
Zhen Xiong,Si Chen,Jinqing Guo,Ningyan Cheng,Shilin Zhang,Binwei Zhang,Zidong Wei,Shi‐Gang Sun,Zaiping Guo
标识
DOI:10.1002/adma.202505966
摘要
Abstract The Na 2 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 2 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 2 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 2 S. This Mo‐Na 2 S/C exhibits remarkable cyclic stability, achieving an initial capacity of 1617 mAh g −1 at 0.1 A g −1 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 −1 . Experimental results and theoretical calculations reveal that the atomic Mo facilitates the interfacial electron transfer between Mo and Na 2 S, which modulates the bandgap of Na 2 S and reduces its reaction barriers to polysulfide, thereby enhancing the reaction kinetics. These findings offer an effective strategy for developing high‐performance Na 2 S cathodes and provide deeper insights into electrode preparation mechanisms.
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