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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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (12/12 displayed)

  • 2011Extended x-ray absorption fine structure study of porous GaSb formed by ion implantation20citations
  • 2010Ion-irradiation-induced amorphization of cobalt nanoparticles45citations
  • 2007Modification of embedded Cu nanoparticles4citations
  • 2007Synthesis and characterization of ion-implanted Pt nanocrystals in SiO220citations
  • 2007Formation and characterization of nanoparticles formed by sequential ion implantation of Au and Co into SiO23citations
  • 2007Ion-irradiation-induced amorphization of Cu nanoparticles embedded in SiO224citations
  • 2007Amorphization of embedded Cu nanocrystals by ion irradiation39citations
  • 2006Structural stability of Cu nanocrystals in SiO2 exposed to high-energy ion irradiation8citations
  • 2006Size-dependent structural disorder in nanocrystalline Cu probed by synchrotron-based X-ray techniques7citations
  • 2005EXAFS comparison of crystalline/continuous and amorphous/porous GaSb8citations
  • 2005Irradiation induced defects in nanocrystalline Cu4citations
  • 2005Disorder in Au and Cu nanocrystals formed by ion implantation into thin SiO213citations

Places of action

Chart of shared publication
Ridgway, M. C.
12 / 38 shared
Glover, C. J.
5 / 12 shared
Kluth, S. M.
3 / 3 shared
Foran, G. J.
10 / 17 shared
Sprouster, D. J.
1 / 5 shared
Kirby, N.
1 / 9 shared
Nordlund, K.
1 / 23 shared
Giulian, R.
3 / 14 shared
Araujo, L. L.
3 / 11 shared
Cookson, D. J.
6 / 7 shared
Llewellyn, D. J.
5 / 11 shared
Dunn, S. G.
1 / 1 shared
Hoy, B.
1 / 1 shared
Chart of publication period
2011
2010
2007
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Co-Authors (by relevance)

  • Ridgway, M. C.
  • Glover, C. J.
  • Kluth, S. M.
  • Foran, G. J.
  • Sprouster, D. J.
  • Kirby, N.
  • Nordlund, K.
  • Giulian, R.
  • Araujo, L. L.
  • Cookson, D. J.
  • Llewellyn, D. J.
  • Dunn, S. G.
  • Hoy, B.
OrganizationsLocationPeople

article

Ion-irradiation-induced amorphization of cobalt nanoparticles

  • Sprouster, D. J.
  • Johannessen, B.
  • Ridgway, M. C.
  • Kirby, N.
  • Nordlund, K.
  • Giulian, R.
  • Araujo, L. L.
Abstract

<p>The amorphization of Co nanoparticles embedded in SiO2 has been investigated by measuring their structure and size, before and after ion irradiation, by x-ray absorption spectroscopy and small-angle x-ray scattering, respectively. Compared to bulk material, unirradiated crystalline nanoparticles exhibited increased structural disorder and a decreased average coordination number as a result of finite-size effects. Upon irradiation, there was no variation in nanoparticle size yet significant structural change. The coordination number decreased further while the mean value (bondlength), variance (Debye-Waller factor), and asymmetry (third cumulant) of the interatomic distance distribution all increased, as consistent with theoretical predictions for an amorphous elemental metal. Furthermore, the interatomic distance distribution for irradiated Co nanoparticles was in excellent agreement with our molecular dynamics simulations for bulk amorphous Co, and we have thus attributed the observed structural changes to the formation of an amorphous phase. Though such a crystalline-to-amorphous phase transformation is not readily achievable in bulk material by ion irradiation, we suggest that the perturbed structural state prior to irradiation and the amorphous surrounding matrix both contribute to nucleating and stabilizing the amorphous phase in irradiated Co nanoparticles. In addition to the structural properties, the vibrational properties of the amorphous phase were also probed, using temperature-dependent x-ray absorption spectroscopy measurements. The Einstein temperature of the unirradiated crystalline nanoparticles was lower than that of bulk material due to loosely bonded surface/interfacial atoms. In contrast, that of the irradiated amorphous nanoparticles was substantially higher than the bulk value. We attribute this apparent bond stiffening to the influence of the rigid surrounding matrix.</p>

Topics
  • nanoparticle
  • impedance spectroscopy
  • surface
  • amorphous
  • phase
  • simulation
  • molecular dynamics
  • cobalt
  • x-ray absorption spectroscopy
  • X-ray scattering