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Synthesis and Characterization of Electrochemically Exfoliated Graphene-Molybdophosphate Hybrid Materials for Charge Storage Devices

Authorized Users Only
2016
Authors
Vujković, Milica
Vidoeski, Bojan
Jovanović, Svetlana P.
Bajuk-Bogdanović, Danica V.
Budimir, Milica
Marković, Zoran M.
Pavlović, Vladimir B.
Todorović-Marković, Biljana
Holclajtner-Antunović, Ivanka D.
Article (Published version)
,
© 2016 Elsevier Ltd.
Metadata
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Abstract
A novel electrochemically exfoliated graphene-molybdophosphoric acid nanohybride (EG-MoPA) was prepared via a simple method. Both scanning electron (SEM) and atomic force microscopy (AFM) results show that MoPA clusters are attached to the surfaces of graphene sheets. By changing the mass ratio of EG-MoPA, the morphology of nanohybrid itself can be significantly modulated, from mostly flat graphene like structure at low amount of MoPA to very uneven, wavy surfaces when MoPA is present in higher concentration. The Raman and Fourier transform infra red (FTIR) spectra in conjunction with electrochemical results indicate that strong interaction exists between the components of nanohybride based on charge transfer and electrostatic interaction of graphene sheets and MoPA. The electrochemical performances are improved by synergetic effect of reversible redox properties of MoPA and the double layer capacitance of a high-surface area of the obtained nanohybrides. The higher current capability ...of EG was achieved by anchoring the small MoPA concentration on the graphene support. The strong bonding of EG with the MoPA prevents acid to dissolve in the electrolyte upon cycling, enabling the stable capacitance behaviour of the low-doped EG sample. The capacitance for the EG doped with the high amount of MoPA was found to be much larger than for EG. However, the obtained capacitance decreases at the beginning of cycling due to the dissolution of excessive amount of surface MoPA, weakly bonded to the graphene support. (C) 2016 Elsevier Ltd. All rights reserved.

Keywords:
exfoliated graphene / polyoxometalates / composite / charge storage devices
Source:
Electrochimica Acta, 2016, 217, 34-46
Funding / projects:
  • SASPRO - Mobility Programme of Slovak Academy of Sciences: Supportive Fund for Excellent Scientists (EU-609427)
  • Electroconducting and redox-active polymers and oligomers: synthesis, structure, properties and applications (RS-172043)
  • Lithium-ion batteries and fuel cells - research and development (RS-45014)
  • Thin films of single wall carbon nanotubes and graphene for electronic application (RS-172003)

DOI: 10.1016/j.electacta.2016.09.067

ISSN: 0013-4686; 1873-3859

WoS: 000385496700005

Scopus: 2-s2.0-84988028740
[ Google Scholar ]
5
5
URI
https://vinar.vin.bg.ac.rs/handle/123456789/1274
Collections
  • WoS Import
Institution/Community
Vinča
TY  - JOUR
AU  - Vujković, Milica
AU  - Vidoeski, Bojan
AU  - Jovanović, Svetlana P.
AU  - Bajuk-Bogdanović, Danica V.
AU  - Budimir, Milica
AU  - Marković, Zoran M.
AU  - Pavlović, Vladimir B.
AU  - Todorović-Marković, Biljana
AU  - Holclajtner-Antunović, Ivanka D.
PY  - 2016
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/1274
AB  - A novel electrochemically exfoliated graphene-molybdophosphoric acid nanohybride (EG-MoPA) was prepared via a simple method. Both scanning electron (SEM) and atomic force microscopy (AFM) results show that MoPA clusters are attached to the surfaces of graphene sheets. By changing the mass ratio of EG-MoPA, the morphology of nanohybrid itself can be significantly modulated, from mostly flat graphene like structure at low amount of MoPA to very uneven, wavy surfaces when MoPA is present in higher concentration. The Raman and Fourier transform infra red (FTIR) spectra in conjunction with electrochemical results indicate that strong interaction exists between the components of nanohybride based on charge transfer and electrostatic interaction of graphene sheets and MoPA. The electrochemical performances are improved by synergetic effect of reversible redox properties of MoPA and the double layer capacitance of a high-surface area of the obtained nanohybrides. The higher current capability of EG was achieved by anchoring the small MoPA concentration on the graphene support. The strong bonding of EG with the MoPA prevents acid to dissolve in the electrolyte upon cycling, enabling the stable capacitance behaviour of the low-doped EG sample. The capacitance for the EG doped with the high amount of MoPA was found to be much larger than for EG. However, the obtained capacitance decreases at the beginning of cycling due to the dissolution of excessive amount of surface MoPA, weakly bonded to the graphene support. (C) 2016 Elsevier Ltd. All rights reserved.
T2  - Electrochimica Acta
T1  - Synthesis and Characterization of Electrochemically Exfoliated Graphene-Molybdophosphate Hybrid Materials for Charge Storage Devices
VL  - 217
SP  - 34
EP  - 46
DO  - 10.1016/j.electacta.2016.09.067
ER  - 
@article{
author = "Vujković, Milica and Vidoeski, Bojan and Jovanović, Svetlana P. and Bajuk-Bogdanović, Danica V. and Budimir, Milica and Marković, Zoran M. and Pavlović, Vladimir B. and Todorović-Marković, Biljana and Holclajtner-Antunović, Ivanka D.",
year = "2016",
abstract = "A novel electrochemically exfoliated graphene-molybdophosphoric acid nanohybride (EG-MoPA) was prepared via a simple method. Both scanning electron (SEM) and atomic force microscopy (AFM) results show that MoPA clusters are attached to the surfaces of graphene sheets. By changing the mass ratio of EG-MoPA, the morphology of nanohybrid itself can be significantly modulated, from mostly flat graphene like structure at low amount of MoPA to very uneven, wavy surfaces when MoPA is present in higher concentration. The Raman and Fourier transform infra red (FTIR) spectra in conjunction with electrochemical results indicate that strong interaction exists between the components of nanohybride based on charge transfer and electrostatic interaction of graphene sheets and MoPA. The electrochemical performances are improved by synergetic effect of reversible redox properties of MoPA and the double layer capacitance of a high-surface area of the obtained nanohybrides. The higher current capability of EG was achieved by anchoring the small MoPA concentration on the graphene support. The strong bonding of EG with the MoPA prevents acid to dissolve in the electrolyte upon cycling, enabling the stable capacitance behaviour of the low-doped EG sample. The capacitance for the EG doped with the high amount of MoPA was found to be much larger than for EG. However, the obtained capacitance decreases at the beginning of cycling due to the dissolution of excessive amount of surface MoPA, weakly bonded to the graphene support. (C) 2016 Elsevier Ltd. All rights reserved.",
journal = "Electrochimica Acta",
title = "Synthesis and Characterization of Electrochemically Exfoliated Graphene-Molybdophosphate Hybrid Materials for Charge Storage Devices",
volume = "217",
pages = "34-46",
doi = "10.1016/j.electacta.2016.09.067"
}
Vujković, M., Vidoeski, B., Jovanović, S. P., Bajuk-Bogdanović, D. V., Budimir, M., Marković, Z. M., Pavlović, V. B., Todorović-Marković, B.,& Holclajtner-Antunović, I. D.. (2016). Synthesis and Characterization of Electrochemically Exfoliated Graphene-Molybdophosphate Hybrid Materials for Charge Storage Devices. in Electrochimica Acta, 217, 34-46.
https://doi.org/10.1016/j.electacta.2016.09.067
Vujković M, Vidoeski B, Jovanović SP, Bajuk-Bogdanović DV, Budimir M, Marković ZM, Pavlović VB, Todorović-Marković B, Holclajtner-Antunović ID. Synthesis and Characterization of Electrochemically Exfoliated Graphene-Molybdophosphate Hybrid Materials for Charge Storage Devices. in Electrochimica Acta. 2016;217:34-46.
doi:10.1016/j.electacta.2016.09.067 .
Vujković, Milica, Vidoeski, Bojan, Jovanović, Svetlana P., Bajuk-Bogdanović, Danica V., Budimir, Milica, Marković, Zoran M., Pavlović, Vladimir B., Todorović-Marković, Biljana, Holclajtner-Antunović, Ivanka D., "Synthesis and Characterization of Electrochemically Exfoliated Graphene-Molybdophosphate Hybrid Materials for Charge Storage Devices" in Electrochimica Acta, 217 (2016):34-46,
https://doi.org/10.1016/j.electacta.2016.09.067 . .

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