Research output: Contribution to journal › Article › peer-review
One-step chemical vapor deposition synthesis and supercapacitor performance of nitrogen-doped porous carbon-carbon nanotube hybrids. / Lobiak, Egor V.; Bulusheva, Lyubov G.; Fedorovskaya, Ekaterina O. et al.
In: Beilstein Journal of Nanotechnology, Vol. 8, No. 1, 12.12.2017, p. 2669-2679.Research output: Contribution to journal › Article › peer-review
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TY - JOUR
T1 - One-step chemical vapor deposition synthesis and supercapacitor performance of nitrogen-doped porous carbon-carbon nanotube hybrids
AU - Lobiak, Egor V.
AU - Bulusheva, Lyubov G.
AU - Fedorovskaya, Ekaterina O.
AU - Shubin, Yury V.
AU - Plyusnin, Pavel E.
AU - Lonchambo, Pierre
AU - Senkovskiy, Boris V.
AU - Ismagilov, Zinfer R.
AU - Flahaut, Emmanuel
AU - Okotrub, Alexander V.
PY - 2017/12/12
Y1 - 2017/12/12
N2 - Novel nitrogen-doped carbon hybrid materials consisting of multiwalled nanotubes and porous graphitic layers have been produced by chemical vapor deposition over magnesium-oxide-supported metal catalysts. CNx nanotubes were grown on Co/Mo, Ni/Mo, or Fe/Mo alloy nanoparticles, and MgO grains served as a template for the porous carbon. The simultaneous formation of morphologically different carbon structures was due to the slow activation of catalysts for the nanotube growth in a carbon-containing gas environment. An analysis of the obtained products by means of transmission electron microscopy, thermogravimetry and X-ray photoelectron spectroscopy methods revealed that the catalyst's composition influences the nanotube/porous carbon ratio and concentration of incorporated nitrogen. The hybrid materials were tested as electrodes in a 1M H2SO4 electrolyte and the best performance was found for a nitrogen-enriched material produced using the Fe/Mo catalyst. From the electrochemical impedance spectroscopy data, it was concluded that the nitrogen doping reduces the resistance at the carbon surface/electrolyte interface and the nanotubes permeating the porous carbon provide fast charge transport in the cell.
AB - Novel nitrogen-doped carbon hybrid materials consisting of multiwalled nanotubes and porous graphitic layers have been produced by chemical vapor deposition over magnesium-oxide-supported metal catalysts. CNx nanotubes were grown on Co/Mo, Ni/Mo, or Fe/Mo alloy nanoparticles, and MgO grains served as a template for the porous carbon. The simultaneous formation of morphologically different carbon structures was due to the slow activation of catalysts for the nanotube growth in a carbon-containing gas environment. An analysis of the obtained products by means of transmission electron microscopy, thermogravimetry and X-ray photoelectron spectroscopy methods revealed that the catalyst's composition influences the nanotube/porous carbon ratio and concentration of incorporated nitrogen. The hybrid materials were tested as electrodes in a 1M H2SO4 electrolyte and the best performance was found for a nitrogen-enriched material produced using the Fe/Mo catalyst. From the electrochemical impedance spectroscopy data, it was concluded that the nitrogen doping reduces the resistance at the carbon surface/electrolyte interface and the nanotubes permeating the porous carbon provide fast charge transport in the cell.
KW - Bimetallic catalyst
KW - Eectrochemical impedance spectroscopy
KW - N-doped carbon
KW - Porous carbon-carbon nanotube hybrid
KW - Supercapacitor
KW - N-2 MOLECULES
KW - ION BATTERIES
KW - electrochemical impedance spectroscopy
KW - porous carbon-carbon nanotube hybrid
KW - OXIDE
KW - GRAPHENE
KW - NANOMATERIALS
KW - NANOPARTICLES
KW - TEMPERATURE
KW - LITHIUM-SULFUR BATTERIES
KW - RAY PHOTOELECTRON-SPECTROSCOPY
KW - ELECTROCHEMICAL CAPACITORS
KW - bimetallic catalyst
KW - supercapacitor
UR - http://www.scopus.com/inward/record.url?scp=85038030023&partnerID=8YFLogxK
U2 - 10.3762/bjnano.8.267
DO - 10.3762/bjnano.8.267
M3 - Article
C2 - 29354339
AN - SCOPUS:85038030023
VL - 8
SP - 2669
EP - 2679
JO - Beilstein Journal of Nanotechnology
JF - Beilstein Journal of Nanotechnology
SN - 2190-4286
IS - 1
ER -
ID: 10065667