Materials Map

Discover the materials research landscape. Find experts, partners, networks.

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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Materials Map under construction

The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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1.080 Topics available

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Naji, M.
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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (4/4 displayed)

  • 2011Tuning percolation speed in layer-by-layer assembled polyaniline–nanocellulose composite films23citations
  • 2011Electron hopping rate measurements in ITO junctions: Charge diffusion in a layer-by-layer deposited ruthenium(II)-bis(benzimidazolyl)pyridine-phosphonate-TiO2 film14citations
  • 2010Carbon nanoparticle surface functionalisation: converting negatively charged sulfonate to positively charged sulfonamide30citations
  • 2010dsDNA modified carbon nanofiber-solidified paste electrodes: probing Ni(II)-dsDNA interactions11citations

Places of action

Chart of shared publication
Edler, Karen J.
1 / 18 shared
Walsh, Darren A.
1 / 3 shared
Marken, Frank
4 / 91 shared
Wasbrough, Matthew J.
1 / 3 shared
Thielemans, Wim
1 / 14 shared
Bonne, Michael J.
1 / 2 shared
Liew, Soon Yee
1 / 1 shared
Shariki, Sara
1 / 3 shared
Cummings, Charles Y.
2 / 6 shared
Parker, Stephen C.
1 / 33 shared
Wadhawan, Jay D.
1 / 4 shared
Nakabayashi, Takuya
1 / 1 shared
Pumera, Martin
1 / 15 shared
Dale, Sara
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Bending, Simon
1 / 6 shared
Haga, Masa-Aki
1 / 1 shared
Nelson, G. W.
1 / 2 shared
Taylor, James
1 / 11 shared
Evans, N. D. M.
1 / 1 shared
Foord, J. S.
1 / 2 shared
Lawrence, R.
1 / 3 shared
Gascon, S. A.
1 / 1 shared
Watkins, John D.
1 / 2 shared
Bull, Steven D.
1 / 2 shared
Wolverson, Daniel
1 / 23 shared
Ferancova, A.
1 / 1 shared
Sillanpaa, M.
1 / 8 shared
Labuda, J.
1 / 1 shared
Chart of publication period
2011
2010

Co-Authors (by relevance)

  • Edler, Karen J.
  • Walsh, Darren A.
  • Marken, Frank
  • Wasbrough, Matthew J.
  • Thielemans, Wim
  • Bonne, Michael J.
  • Liew, Soon Yee
  • Shariki, Sara
  • Cummings, Charles Y.
  • Parker, Stephen C.
  • Wadhawan, Jay D.
  • Nakabayashi, Takuya
  • Pumera, Martin
  • Dale, Sara
  • Bending, Simon
  • Haga, Masa-Aki
  • Nelson, G. W.
  • Taylor, James
  • Evans, N. D. M.
  • Foord, J. S.
  • Lawrence, R.
  • Gascon, S. A.
  • Watkins, John D.
  • Bull, Steven D.
  • Wolverson, Daniel
  • Ferancova, A.
  • Sillanpaa, M.
  • Labuda, J.
OrganizationsLocationPeople

article

Carbon nanoparticle surface functionalisation: converting negatively charged sulfonate to positively charged sulfonamide

  • Nelson, G. W.
  • Taylor, James
  • Marken, Frank
  • Evans, N. D. M.
  • Rassaei, Liza
  • Foord, J. S.
  • Lawrence, R.
  • Gascon, S. A.
  • Watkins, John D.
  • Bull, Steven D.
  • Wolverson, Daniel
Abstract

The surface functionalities of commercial sulfonate-modified carbon nanoparticles (ca. 9-18 nm diameter, Emperor 2000) have been converted from negatively charged to positively charged via sulfonylchloride formation followed by reaction with amines to give suphonamides. With ethylenediamine, the resulting positively charged carbon nanoparticles exhibit water solubility (in the absence of added electrolyte), a positive zeta-potential, and the ability to assemble into insoluble porous carbon films via layer-by-layer deposition employing alternating positive and negative carbon nanoparticles. Sulfonamide-functionalised carbon nanoparticles are characterised by Raman, AFM, XPS, and voltammetric methods. Stable thin film deposits are formed on 3 mm diameter glassy carbon electrodes and cyclic voltammetry is used to characterise capacitive background currents and the adsorption of the negatively charged redox probe indigo carmine. The Langmuirian binding constant K = 4000 mol(-1) dm(3) is estimated and the number of positively charged binding sites per particle determined as a function of pH.

Topics
  • nanoparticle
  • Deposition
  • porous
  • impedance spectroscopy
  • surface
  • Carbon
  • thin film
  • x-ray photoelectron spectroscopy
  • atomic force microscopy
  • amine
  • cyclic voltammetry