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The recent development of synthesis processes for three-dimensional (3D) graphene-based structures has tended to focus on continuous improvement of porous nanostructures, doping modification during thin-film fabrication, and mechanisms for building 3D architectures. Here, we synthesized novel snowflake-like Si-O/Si-C nanostructures on 3D graphene/Cu foam by one-step low-pressure chemical vapor deposition (CVD). Through systematic micromorphological characterization, it was determined that the formation mechanism of the nanostructures involved the melting of the Cu foam surface and the subsequent condensation of the resulting vapor, 3D growth of graphene through catalysis in the presence of Cu, and finally, nucleation of the Si-O/Si-C nanostructure in the carbon-rich atmosphere. Thus, by tuning the growth temperature and duration, it should be possible to control the nucleation and evolution of such snowflake-like nanostructures with precision. Electrochemical measurements indicated that the snowflake-like nanostructures showed excellent performance as a material for energy storage. The highest specific capacitance of the Si-O/Si-C nanostructures was ~963.2 mF/cm2 at a scan rate of 1 mV/s. Further, even after 20, 000 sequential cycles, the electrode retained 94.4% of its capacitance.

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Publication history
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Acknowledgements

Publication history

Received: 10 June 2017
Revised: 13 August 2017
Accepted: 15 August 2017
Published: 19 March 2018
Issue date: April 2018

Copyright

© Tsinghua University Press and Springer-Verlag GmbH Germany 2017

Acknowledgements

Acknowledgements

The work was supported by the National Natural Science Foundation of China (Nos. 61604115 and 61334002), the Natural Science Basic Research Plan in Shaanxi Province of China (No. 2016ZDJC-09), the Key Research and Development program in Shaanxi Province (No. 2017ZDCXL-GY-11-03), the China Postdoctoral Science Foundation (No. 2015M580814), the Postdoctoral Science Research Plan in Shaanxi Province of China and the Fundamental Research Funds for the Central Universities (Nos. XJS15066 and JB161103).

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