Materials Map

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

  • About
  • Privacy Policy
  • Legal Notice
  • Contact

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.

×

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.

To Graph

1.080 Topics available

To Map

977 Locations available

693.932 PEOPLE
693.932 People People

693.932 People

Show results for 693.932 people that are selected by your search filters.

←

Page 1 of 27758

→
←

Page 1 of 0

→
PeopleLocationsStatistics
Naji, M.
  • 2
  • 13
  • 3
  • 2025
Motta, Antonella
  • 8
  • 52
  • 159
  • 2025
Aletan, Dirar
  • 1
  • 1
  • 0
  • 2025
Mohamed, Tarek
  • 1
  • 7
  • 2
  • 2025
Ertürk, Emre
  • 2
  • 3
  • 0
  • 2025
Taccardi, Nicola
  • 9
  • 81
  • 75
  • 2025
Kononenko, Denys
  • 1
  • 8
  • 2
  • 2025
Petrov, R. H.Madrid
  • 46
  • 125
  • 1k
  • 2025
Alshaaer, MazenBrussels
  • 17
  • 31
  • 172
  • 2025
Bih, L.
  • 15
  • 44
  • 145
  • 2025
Casati, R.
  • 31
  • 86
  • 661
  • 2025
Muller, Hermance
  • 1
  • 11
  • 0
  • 2025
Kočí, JanPrague
  • 28
  • 34
  • 209
  • 2025
Šuljagić, Marija
  • 10
  • 33
  • 43
  • 2025
Kalteremidou, Kalliopi-ArtemiBrussels
  • 14
  • 22
  • 158
  • 2025
Azam, Siraj
  • 1
  • 3
  • 2
  • 2025
Ospanova, Alyiya
  • 1
  • 6
  • 0
  • 2025
Blanpain, Bart
  • 568
  • 653
  • 13k
  • 2025
Ali, M. A.
  • 7
  • 75
  • 187
  • 2025
Popa, V.
  • 5
  • 12
  • 45
  • 2025
Rančić, M.
  • 2
  • 13
  • 0
  • 2025
Ollier, Nadège
  • 28
  • 75
  • 239
  • 2025
Azevedo, Nuno Monteiro
  • 4
  • 8
  • 25
  • 2025
Landes, Michael
  • 1
  • 9
  • 2
  • 2025
Rignanese, Gian-Marco
  • 15
  • 98
  • 805
  • 2025

Murphy, Maria A.

  • Google
  • 2
  • 4
  • 44

in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (2/2 displayed)

  • 2003Sonoelectrochemistry of molecular and colloidal redox systems at carbon nanofiber-ceramic composite electrodes17citations
  • 2003Adsorption and redox processes at carbon nanofiber electrodes grown onto a ceramic fiber backbone27citations

Places of action

Chart of shared publication
Marken, Frank
2 / 91 shared
Mocak, Jan
1 / 1 shared
Wilcox, Geoff D.
1 / 1 shared
Dahm, Ralf H.
1 / 2 shared
Chart of publication period
2003

Co-Authors (by relevance)

  • Marken, Frank
  • Mocak, Jan
  • Wilcox, Geoff D.
  • Dahm, Ralf H.
OrganizationsLocationPeople

article

Sonoelectrochemistry of molecular and colloidal redox systems at carbon nanofiber-ceramic composite electrodes

  • Murphy, Maria A.
  • Marken, Frank
  • Mocak, Jan
Abstract

<p>An electrically conducting composite electrode consisting of a ceramic paper substrate, which has been densely coated with carbon nanofibers of ca. 100 nm diameter, is employed in the presence of 24 kHz (8 W cm<sup>-2</sup>) power ultrasound emitted from a glass horn system. The carbon composite electrode remains stable during prolonged use in the presence of ultrasound. Sonovoltammetric limiting currents for the reduction of Ru(NH<sub>3</sub>) <sub>6</sub><sup>3+</sup>, the oxidation of hydroquinone, and the reduction of colloidal hydrous iron oxide are reported. A comparison of sonovoltammograms obtained at a porous carbon nanofiber-ceramic composite electrode with those obtained at a conventional glassy carbon electrode shows that (i) the average mass transport limited current density at carbon nanofiber-ceramic composite electrodes is increased by approximately one order of magnitude, and (ii) due to the porous topography of the electrode surface, molecules remain resident within the diffusion layer for a longer period of time. Colloidal hydrous iron oxide is not reduced at conventional glassy carbon electrodes but can be reduced at the porous carbon nanofiber-ceramic composite electrode, presumably due to a more effective particle-carbon nanofiber electrode surface interaction.</p>

Topics
  • porous
  • density
  • impedance spectroscopy
  • surface
  • Carbon
  • glass
  • glass
  • composite
  • iron
  • current density
  • ceramic