材料科学
钴
钠
Atom(片上系统)
碳纤维
兴奋剂
碳原子
化学工程
复合材料
光电子学
冶金
化学
有机化学
戒指(化学)
复合数
计算机科学
嵌入式系统
工程类
作者
Xia Wen,Feng Wang,Xiaohui Li,Junbo Yang,Ruofan Du,Peng Wang,Hui Li,Luying Song,Yuzu Wang,Mo Cheng,Jun He,Jianping Shi
标识
DOI:10.1002/adma.202211690
摘要
2D transition metal dichalcogenides (TMDCs) and single-atom catalysts (SACs) are promising electrodes for energy conversion/storage because of the layered structure and maximum atom utilization efficiency. However, the integration of such two type materials and the relevant sodium storage applications remain daunting challenges. Here, an ingenious diatomite-templated synthetic strategy is designed to fabricate single-atom cobalt-doped MoS2 /carbon (SA Co-MoS2 /C) composites toward the high-performance sodium storage. Benefiting from the unique hierarchical structure, high electron/sodium-ion conductivity, and abundant active sites, the obtained SA Co-MoS2 /C reveals remarkable specific capacity (≈604.0 mAh g-1 at 0.1 A g-1 ), high rate performance, and outstanding long cyclic stability. Particularly, the sodium-ion full cell composed of SA Co-MoS2 /C anode and Na3 V2 (PO4 )3 cathode demonstrates unexpected stability with the cycle number exceeded 1200. The internal sodium storage mechanism is clarified with the aid of density functional theory calculations and in situ experimental characterizations. This work not only represents a substantial leap in terms of synthesizing SACs on 2D TMDCs but also provides a crucial step toward the practical sodium-ion battery applications.
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