4.8 Article

Delicate Co-Control of Shell Structure and Sulfur Vacancies in Interlayer-Expanded Tungsten Disulfide Hollow Sphere for Fast and Stable Sodium Storage

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ADVANCED MATERIALS
卷 35, 期 7, 页码 -

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WILEY-V C H VERLAG GMBH
DOI: 10.1002/adma.202209354

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expanded interlayer spacing; hollow multishelled structure; sodium storage; sulfur vacancies; transition-metal sulfides

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Hollow multishelled structure (HoMS) is a promising platform for energy storage due to its unique temporal-spatial ordering property and buffering function. In this study, a sequential sulfidation and etching approach is developed to achieve co-control over the molecular- and nano-/micro-scale structures of WS2-x HoMS. The obtained WS2-x HoMS with sulfur vacancies and expanded interlayer spacing demonstrates superior performance for sodium storage. This finding offers prospects for practical fast-charging, high-energy, and long-cycling sodium storage.
Hollow multishelled structure (HoMS) is a promising multi-functional platform for energy storage, owing to its unique temporal-spatial ordering property and buffering function. Accurate co-control of its multiscale structures may bring fascinating properties and new opportunities, which is highly desired yet rarely achieved due to the challenging synthesis. Herein, a sequential sulfidation and etching approach is developed to achieve the delicate co-control over both molecular- and nano-/micro-scale structure of WS2-x HoMS. Typically, sextuple-shelled WS2-x HoMS with abundant sulfur vacancies and expanded-interlayer spacing is obtained from triple-shelled WO3 HoMS. By further coating with nitrogen-doped carbon, WS2-x HoMS maintains a reversible capacity of 241.7 mAh g(-1) at 5 A g(-1) after 1000 cycles for sodium storage, which is superior to the previously reported results. Mechanism analyses reveal that HoMS provides good electrode-electrolyte contact and plentiful sodium storage sites as well as an effective buffer of the stress/strain during cycling; sulfur vacancy and expanded interlayer of WS2-x enhance ion diffusion kinetics; carbon coating improves the electron conductivity and benefits the structural stability. This finding offers prospects for realizing practical fast-charging, high-energy, and long-cycling sodium storage.

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