Carbon-coated MoS1.5Te0.5 nanocables for efficient sodium-ion storage in non-aqueous dual-ion batteries

Sodium-based dual-ion batteries have received increased attention owing to their appealing cell voltage (i.e., >3 V) and cost-effective features. However, the development of high-performance anode materials is one of the key elements for exploiting this electrochemical energy storage system at pr...

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Published inNature communications Vol. 13; no. 1; p. 663
Main Authors Liu, Yangjie, Hu, Xiang, Li, Junwei, Zhong, Guobao, Yuan, Jun, Zhan, Hongbing, Tang, Yongbing, Wen, Zhenhai
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 03.02.2022
Nature Publishing Group
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Summary:Sodium-based dual-ion batteries have received increased attention owing to their appealing cell voltage (i.e., >3 V) and cost-effective features. However, the development of high-performance anode materials is one of the key elements for exploiting this electrochemical energy storage system at practical levels. Here, we report a source-template synthetic strategy for fabricating a variety of nanowire-in-nanotube MS x Te y @C (M = Mo, W, Re) structures with an in situ-grown carbon film coating, termed as nanocables. Among the various materials prepared, the MoS 1.5 Te 0.5 @C nanocables are investigated as negative electrode active material in combination with expanded graphite at the positive electrode and NaPF 6 -based non-aqueous electrolyte solutions for dual-ion storage in coin cell configuration. As a result, the dual-ion lab-scale cells demonstrate a prolonged cycling lifespan with 97% capacity retention over 1500 cycles and a reversible capacity of about 101 mAh g −1 at specific capacities (based on the mass of the anode) of 1.0 A g −1 and 5.0 A g −1 , respectively. Sodium-based dual-ion batteries are promising electrochemical energy storage devices. Here, the authors report a source-template synthetic strategy to prepare carbon-coated MoS 1.5 Te 0.5 nanocables and their use as anode active materials in Na-based dual ion cells.
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ISSN:2041-1723
2041-1723
DOI:10.1038/s41467-022-28176-0