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Boosting Sodium Storage of Fe(1−x)S/MoS(2) Composite via Heterointerface Engineering
Improving the cycling stability of metal sulfide-based anode materials at high rate is of great significance for advanced sodium ion batteries. However, the sluggish reaction kinetics is a big obstacle for the development of high-performance sodium storage electrodes. Herein, we have rationally engi...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Singapore
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7770956/ https://www.ncbi.nlm.nih.gov/pubmed/34138042 http://dx.doi.org/10.1007/s40820-019-0311-z |
Sumario: | Improving the cycling stability of metal sulfide-based anode materials at high rate is of great significance for advanced sodium ion batteries. However, the sluggish reaction kinetics is a big obstacle for the development of high-performance sodium storage electrodes. Herein, we have rationally engineered the heterointerface by designing the Fe(1−x)S/MoS(2) heterostructure with abundant “ion reservoir” to endow the electrode with excellent cycling stability and rate capability, which is proved by a series of in and ex situ electrochemical investigations. Density functional theory calculations further reveal that the heterointerface greatly decreases sodium ion diffusion barrier and facilitates charge-transfer kinetics. Our present findings not only provide a deep analysis on the correlation between the structure and performance, but also draw inspiration for rational heterointerface engineering toward the next-generation high-performance energy storage devices. [Image: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s40820-019-0311-z) contains supplementary material, which is available to authorized users. |
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