High-capacity antimony sulphide nanoparticle-decorated graphene composite as anode for sodium-ion batteries

Sodium-ion batteries are an alternative to lithium-ion batteries for large-scale applications. However, low capacity and poor rate capability of existing anodes are the main bottlenecks to future developments. Here we report a uniform coating of antimony sulphide (stibnite) on graphene, fabricated b...

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Published inNature communications Vol. 4; no. 1; p. 2922
Main Authors Yu, Denis Y. W., Prikhodchenko, Petr V., Mason, Chad W., Batabyal, Sudip K., Gun, Jenny, Sladkevich, Sergey, Medvedev, Alexander G., Lev, Ovadia
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 10.12.2013
Nature Publishing Group
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Summary:Sodium-ion batteries are an alternative to lithium-ion batteries for large-scale applications. However, low capacity and poor rate capability of existing anodes are the main bottlenecks to future developments. Here we report a uniform coating of antimony sulphide (stibnite) on graphene, fabricated by a solution-based synthesis technique, as the anode material for sodium-ion batteries. It gives a high capacity of 730 mAh g −1 at 50 mA g −1 , an excellent rate capability up to 6C and a good cycle performance. The promising performance is attributed to fast sodium ion diffusion from the small nanoparticles, and good electrical transport from the intimate contact between the active material and graphene, which also provides a template for anchoring the nanoparticles. We also demonstrate a battery with the stibnite–graphene composite that is free from sodium metal, having energy density up to 80 Wh kg −1 . The energy density could exceed that of some lithium-ion batteries with further optimization. Anode materials used for sodium-ion batteries often suffer from poor stability and rate capability in electrochemical reactions. Yu et al. report a nanocomposite anode consisting of stibnite and reduced graphene oxide, which exhibits excellent cycle stability and rate performance.
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ISSN:2041-1723
2041-1723
DOI:10.1038/ncomms3922