Nanosized core-shell structured graphene-MnO2 nanosheet arrays as stable electrodes for superior supercapacitorsElectronic supplementary information (ESI) available. See DOI: 10.1039/c7ta02627g
Directly fabricating vertically standing graphene-manganese dioxide (MnO 2 ) nanoparticle hybrids as electrode materials remains a challenge, especially so without the use of organic binders. Such hybrids should exhibit high electrochemical performance and high stability. To address this challenge,...
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Main Authors | , , , , , , , |
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Format | Journal Article |
Language | English |
Published |
30.05.2017
|
Online Access | Get full text |
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Summary: | Directly fabricating vertically standing graphene-manganese dioxide (MnO
2
) nanoparticle hybrids as electrode materials remains a challenge, especially so without the use of organic binders. Such hybrids should exhibit high electrochemical performance and high stability. To address this challenge, we report a strategy for fabricating nanosized core-shell graphene-MnO
2
nanosheet arrays (G-MnO
2
NAs) for use as electrodes for supercapacitors. The as-grown MnO
2
nanosheets are transformed into core-shell G-MnO
2
nanoparticles by plasma-enhanced chemical vapor deposition. The
in situ
formed graphene layers act as binders and frameworks, and provide integrity and stability to the overall nanosheet. The resulting core-shell nanoparticles exhibit a high specific surface area and long-term cycling stability. The synergistic effect of the vertically standing intercalated architecture and
in situ
formed graphene provides a short ion diffusion pathway and a high conductivity. The G-MnO
2
NAs exhibit a high specific capacitance of 1176 F g
−1
at 2 mV s
−1
, and a long cycling lifetime with negligible capacitance loss after 10 000 cycles. This process for the
in situ
formation of graphene may be useful for improving the electrochemical performance of other metal oxide-based electrodes.
Directly fabricating vertically standing graphene-manganese dioxide (MnO
2
) nanoparticle hybrids as electrode materials remains a challenge, especially so without the use of organic binders. |
---|---|
Bibliography: | 10.1039/c7ta02627g Electronic supplementary information (ESI) available. See DOI |
ISSN: | 2050-7488 2050-7496 |
DOI: | 10.1039/c7ta02627g |