Issue 22, 2012

Columnar assembly and successive heating of colloidal 2D nanomaterials on graphene as an efficient strategy for new anode materials in lithium ion batteries: the case of In2S3 nanoplates

Abstract

This study shows that heat-treatment of colloidal inorganic nanoplates with columnar assembly under argon is a good strategy for development of anode materials. The heating of colloidal In2S3 nanoplates under argon resulted in the formation of film-like materials through interconnection of plates in a side by side manner. When the columnarly assembled colloidal In2S3 plates were heated at 400 °C under argon for 2 hours on graphene, more efficient anode materials with smaller diameters were obtained. Interestingly, the heat-treated columnarly assembled In2S3 plates on graphene had a layered structure, which was attributed to the possible existence of carbon materials between plates formed by the heat-treatment of surfactants under argon. The resultant graphene–In2S3 composites showed enhanced discharge capacities, up to 716–837 mA h g−1, as well as excellent stabilities. In addition, the materials showed promising coulombic efficiencies and rate performances. We believe that, based on the strategy in this work, diverse graphene–inorganic nanomaterial composites with a layered structure can be prepared and applied as new anode materials in lithium ion batteries.

Graphical abstract: Columnar assembly and successive heating of colloidal 2D nanomaterials on graphene as an efficient strategy for new anode materials in lithium ion batteries: the case of In2S3 nanoplates

Supplementary files

Article information

Article type
Paper
Submitted
15 Feb 2012
Accepted
29 Mar 2012
First published
29 Mar 2012

J. Mater. Chem., 2012,22, 11107-11112

Columnar assembly and successive heating of colloidal 2D nanomaterials on graphene as an efficient strategy for new anode materials in lithium ion batteries: the case of In2S3 nanoplates

J. Choi, J. Jin, J. Lee, J. H. Park, H. J. Kim, D. Oh, J. R. Ahn and S. U. Son, J. Mater. Chem., 2012, 22, 11107 DOI: 10.1039/C2JM30949A

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