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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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 (4/4 displayed)

  • 2021Twin boundary migration in an individual platinum nanocrystal during catalytic CO oxidation36citations
  • 2021When more is less: plastic weakening of single crystalline Ag nanoparticles by the polycrystalline Au shell12citations
  • 2019Grain growth and solid-state dewetting of Bi-Crystal Ni-Fe thin films on sapphire21citations
  • 2018Nickel nanoparticles set a new record of strength103citations

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Chart of shared publication
Hofmann, Jan, P.
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Texier, Michaël
1 / 1 shared
Carnis, Jérôme
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Favre, Luc
1 / 25 shared
Rabkin, Eugen
3 / 28 shared
Almog, Ehud
1 / 4 shared
Oropeza, Freddy, E.
1 / 1 shared
Schülli, Tobias, U.
1 / 3 shared
Campos, Andrea
1 / 8 shared
Micha, Jean-Sébastien
1 / 13 shared
Thomas, Olivier
2 / 26 shared
Leake, Steven, J.
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Wu, Longfei
1 / 10 shared
Poloni, Roberta
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Richard, Marieingrid
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Gao, Lu
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Hensen, Emiel, J. M.
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Labat, Stéphane
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Kshirsagar, Aseem, Rajan
1 / 1 shared
Dupraz, Maxime
1 / 12 shared
Sharma, Amit
2 / 26 shared
Qi, Yuanshen
1 / 6 shared
Amodeo, Jonathan
1 / 17 shared
Kumar, Aakash
1 / 1 shared
Srolovitz, David
1 / 65 shared
Sharma, A.
1 / 38 shared
Mishin, Y.
1 / 2 shared
Rabkin, E.
1 / 8 shared
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2019
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Co-Authors (by relevance)

  • Hofmann, Jan, P.
  • Texier, Michaël
  • Carnis, Jérôme
  • Favre, Luc
  • Rabkin, Eugen
  • Almog, Ehud
  • Oropeza, Freddy, E.
  • Schülli, Tobias, U.
  • Campos, Andrea
  • Micha, Jean-Sébastien
  • Thomas, Olivier
  • Leake, Steven, J.
  • Wu, Longfei
  • Poloni, Roberta
  • Richard, Marieingrid
  • Gao, Lu
  • Hensen, Emiel, J. M.
  • Labat, Stéphane
  • Kshirsagar, Aseem, Rajan
  • Dupraz, Maxime
  • Sharma, Amit
  • Qi, Yuanshen
  • Amodeo, Jonathan
  • Kumar, Aakash
  • Srolovitz, David
  • Sharma, A.
  • Mishin, Y.
  • Rabkin, E.
OrganizationsLocationPeople

article

Grain growth and solid-state dewetting of Bi-Crystal Ni-Fe thin films on sapphire

  • Gazit, Nimrod
  • Rabkin, Eugen
  • Kumar, Aakash
  • Sharma, Amit
  • Srolovitz, David
Abstract

We studied the solid-state dewetting behavior of thin Ni<sub>80</sub>Fe<sub>20</sub>films deposited on basal plane oriented sapphire substrate and annealed in the range of temperatures of 1023–1323 K. All studied films exhibited strong &lt;111&gt; texture and maze bicrystal microstructure, with only two grains misoriented by 60° around the common &lt;111&gt; axis present in the film. The morphology of partially dewetted films changed from the one typical for polycrystalline thin films to the one typical for single crystalline heteroepitaxial films with increasing temperatures and annealing times. This change of dewetting behavior was associated with the fast grain growth in the films. The films of pure Ni of identical thickness, annealed under identical conditions exhibited significantly slower grain growth and lower thermal stability. Both the high-resolution X-ray diffraction and the cross-sectional high-resolution transmission electron microscopy observations revealed the phase separation of the Ni<sub>80</sub>Fe<sub>20</sub>films into two parallel layers of the face-centered cubic (adjacent to the substrate) and hexagonal close-packed (on the top of the film) phases of similar compositions. Our density functional theory (DFT) calculations indicated that this phase separation is driven by the decrease of the film surface and interface energy, leading to the thermodynamically equilibrium thickness of the metastable hexagonal close-packed phase. This phase exhibits higher surface anisotropy than its stable face-centered cubic counterpart and is instrumental in accelerating the grain growth in the film via suppression of grain boundary grooving.

Topics
  • density
  • impedance spectroscopy
  • surface
  • grain
  • phase
  • grain boundary
  • x-ray diffraction
  • theory
  • thin film
  • transmission electron microscopy
  • texture
  • density functional theory
  • annealing
  • grain growth