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 (7/7 displayed)

  • 2019Thermal stability and irradiation response of nanocrystalline CoCrCuFeNi high-entropy alloy65citations
  • 2018A(2)TiO(5) (A = Dy, Gd, Er, Yb) at High Pressurecitations
  • 2018Radiation-induced disorder in compressed lanthanide zirconatescitations
  • 2015Response of Gd2Ti2O7 and La2Ti2O7 to swift-heavy ion irradiation and annealing71citations
  • 2014Swift heavy ion irradiation-induced amorphization of La2Ti2O724citations
  • 2014Swift heavy ion irradiation-induced amorphization of $La_2Ti_2O_7$24citations
  • 2012Swift heavy ion-induced amorphization of $CaZrO_{3}$ perovskite32citations

Places of action

Chart of shared publication
Weber, William J.
1 / 10 shared
Boldman, Walker L.
1 / 2 shared
Jiang, Li
1 / 2 shared
Xu, Chen
1 / 1 shared
Rack, Philip D.
1 / 8 shared
Wang, Lumin
1 / 1 shared
Donnelly, Stephen E.
1 / 7 shared
Zhang, Yanwen
1 / 22 shared
Greaves, Graeme
1 / 26 shared
Tunes, Matheus Araujo
1 / 34 shared
Crespillo, Miguel L.
1 / 1 shared
Tracy, Cameron L.
5 / 7 shared
Ewing, Rodney C.
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Oquinn, Eric
1 / 4 shared
Mao, Wendy L.
1 / 4 shared
Rittman, Dylan R.
1 / 2 shared
Chapman, Karena W.
1 / 19 shared
Park, Sulgiye
5 / 7 shared
Lang, Maik
6 / 13 shared
Park, Changyong
2 / 3 shared
Shamblin, Jacob
1 / 1 shared
Tkachev, Sergey N.
2 / 2 shared
Maoah, Wendy L.
1 / 1 shared
Trautmann, Christina
5 / 35 shared
Rodriguez, Matias D.
3 / 3 shared
Zhang, Jiaming
3 / 4 shared
Kluth, Patrick
1 / 7 shared
Klaumünzer, Siegfried
1 / 1 shared
Li, Weixing
1 / 1 shared
Bender, Markus
1 / 4 shared
Severin, Daniel
1 / 5 shared
Chart of publication period
2019
2018
2015
2014
2012

Co-Authors (by relevance)

  • Weber, William J.
  • Boldman, Walker L.
  • Jiang, Li
  • Xu, Chen
  • Rack, Philip D.
  • Wang, Lumin
  • Donnelly, Stephen E.
  • Zhang, Yanwen
  • Greaves, Graeme
  • Tunes, Matheus Araujo
  • Crespillo, Miguel L.
  • Tracy, Cameron L.
  • Ewing, Rodney C.
  • Oquinn, Eric
  • Mao, Wendy L.
  • Rittman, Dylan R.
  • Chapman, Karena W.
  • Park, Sulgiye
  • Lang, Maik
  • Park, Changyong
  • Shamblin, Jacob
  • Tkachev, Sergey N.
  • Maoah, Wendy L.
  • Trautmann, Christina
  • Rodriguez, Matias D.
  • Zhang, Jiaming
  • Kluth, Patrick
  • Klaumünzer, Siegfried
  • Li, Weixing
  • Bender, Markus
  • Severin, Daniel
OrganizationsLocationPeople

article

Swift heavy ion irradiation-induced amorphization of La2Ti2O7

  • Tracy, Cameron L.
  • Ewing, Rodney C.
  • Zhang, Fuxiang
  • Park, Sulgiye
  • Lang, Maik
  • Rodriguez, Matias D.
  • Trautmann, Christina
  • Zhang, Jiaming
Abstract

<p>Polycrystalline La<sub>2</sub>Ti<sub>2</sub>O<sub>7</sub> powders have been irradiated with 2.0 GeV <sup>181</sup>Ta ions up to a fluence of 1 × 10<sup>13</sup> ions/cm<sup>2</sup>. Radiation-induced structural modifications were analyzed using synchrotron-based X-ray diffraction (XRD), small angle X-ray scattering (SAXS), Raman spectroscopy and transmission electron microscopy (TEM). An increase in the amorphous fraction as a function of fluence was revealed by XRD and Raman analyses and is evidenced by the reduction in intensity of the sharp Bragg maxima from the crystalline regions. Concurrently, diffraction maxima and vibrational absorption bands broaden with the increasing amorphous fraction. The cross-section for the crystalline-to-amorphous transformation (ion tracks) was determined by quantitative analysis of XRD patterns yielding a track diameter of d = 7.2 ± 0.9 nm. Slightly larger track diameters were obtained directly from TEM images (d = 10.6 ± 0.8 nm) and SAXS analysis (d = 10.6 ± 0.3 nm). High-resolution TEM images revealed that single tracks are entirely amorphous without any outer crystalline, disordered shell as found in pyrochlore oxides of the same stoichiometry. The large ratio of ionic radii of the A- and B-site cations (r<sub>A</sub>/r<sub>B</sub> = 1.94) means that disordering over the A- and B-sites is energetically unfavorable.</p>

Topics
  • impedance spectroscopy
  • amorphous
  • x-ray diffraction
  • transmission electron microscopy
  • Raman spectroscopy
  • small angle x-ray scattering
  • quantitative determination method