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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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.

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Naji, M.
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Hess, Wayne P.

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (16/16 displayed)

  • 2013Photoemission Electron Microscopy of a Plasmonic Silver Nanoparticle Trimer10citations
  • 2013Silver nanorod arrays for photocathode applications17citations
  • 2013Plasmon-Induced Optical Field Enhancement studied by Correlated Scanning and Photoemission Electron Microscopy17citations
  • 2012Near-field focused photoemission from polystyrene microspheres studied with photoemission electron microscopy6citations
  • 2011Plasmonic enhancement of thin-film solar cells using gold-black coatings2citations
  • 2011Plasmonic Field Enhancement of Individual Nanoparticles by Correlated Scanning and Photoemission Electron Microscopy30citations
  • 2010Effect of Surface Charge on Laser-induced Neutral Atom Desorption1citations
  • 2007An In Situ Study of the Martensitic Transformation in Shape Memory Alloys Using Photoemission Electron Microscopy7citations
  • 2007Study of Martensitic Phase transformation in a NiTiCu Thin Film Shape Memory Alloy Using Photoelectron Emission Microscopy13citations
  • 2007Real Time Study of Cu Diffusion Through a Ru Thin Film by Photoemission Electron Microscopy (PEEM)citations
  • 2007Study of Copper Diffusion Through Ruthenium Thin Film by Photoemission Electron Microscopy12citations
  • 2007Photoemission Electron Microscopy of TiO2 Anatase Films Embedded with Rutile Nanocrystals177citations
  • 2006In Situ Photoelectron Emission Microscopy of a Thermally Induced Martensitic Transformation in a CuZnAI Shape Memory Alloy10citations
  • 2006Laser-Induced Oxygen Vacancy Formation and Diffusion on TiO2(110) Surfaces Probed by Photoemission Electron Microscopy8citations
  • 2005Surface Electronic Properties and Site-Specific Laser Desorption Processes of Highly Structured Nanoporous MgO Thin Films12citations
  • 2002"EXAFS Study of Rare-Earth Element Coordination in Calcite"73citations

Places of action

Chart of shared publication
Wei, Wei
3 / 7 shared
Wang, Yi-Chung
1 / 1 shared
Wang, Jinyong
1 / 1 shared
Joly, Alan G.
15 / 16 shared
Peppernick, Samuel J.
5 / 5 shared
Beck, Kenneth M.
14 / 17 shared
Kayani, Asghar N.
1 / 1 shared
Pandey, Archana
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Schwenzer, Birgit
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El-Khoury, Patrick Z.
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Nandasiri, Manjula I.
1 / 1 shared
Vilayurganapathy, Subramanian
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Varga, Tamas
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Coffey, Greg W.
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Thevuthasan, Suntharampillai
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Fredricksen, Christopher J.
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Rezaie, F. K.
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Figueiredo, P. N.
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Arnold, J. P.
1 / 1 shared
Panjwani, D. R.
1 / 1 shared
Baillie, K.
1 / 1 shared
Colwell, J. E.
1 / 4 shared
Peale, Robert E.
2 / 2 shared
Dickinson, J. T.
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Langford, Stephen C.
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Droubay, Timothy C.
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Cai, Mingdong
3 / 3 shared
Xiong, Gang
7 / 9 shared
Beck, Kenneth
1 / 1 shared
Wu, Maggie J.
1 / 1 shared
Huang, W. M.
1 / 1 shared
Sun, Yuming
1 / 1 shared
White, J. M.
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Sun, Y.
1 / 12 shared
Parker, S. L.
1 / 1 shared
Shao, Rui
1 / 1 shared
Chambers, Scott A.
1 / 6 shared
Henyk, Matthias
1 / 1 shared
Engelhard, Mark H.
1 / 4 shared
Reeder, Richard
1 / 1 shared
Elzinga, E. J.
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Withers, S. H.
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Mason, R. A.
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Chart of publication period
2013
2012
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Co-Authors (by relevance)

  • Wei, Wei
  • Wang, Yi-Chung
  • Wang, Jinyong
  • Joly, Alan G.
  • Peppernick, Samuel J.
  • Beck, Kenneth M.
  • Kayani, Asghar N.
  • Pandey, Archana
  • Schwenzer, Birgit
  • El-Khoury, Patrick Z.
  • Nandasiri, Manjula I.
  • Vilayurganapathy, Subramanian
  • Varga, Tamas
  • Coffey, Greg W.
  • Thevuthasan, Suntharampillai
  • Fredricksen, Christopher J.
  • Rezaie, F. K.
  • Figueiredo, P. N.
  • Arnold, J. P.
  • Panjwani, D. R.
  • Baillie, K.
  • Colwell, J. E.
  • Peale, Robert E.
  • Dickinson, J. T.
  • Langford, Stephen C.
  • Droubay, Timothy C.
  • Cai, Mingdong
  • Xiong, Gang
  • Beck, Kenneth
  • Wu, Maggie J.
  • Huang, W. M.
  • Sun, Yuming
  • White, J. M.
  • Sun, Y.
  • Parker, S. L.
  • Shao, Rui
  • Chambers, Scott A.
  • Henyk, Matthias
  • Engelhard, Mark H.
  • Reeder, Richard
  • Elzinga, E. J.
  • Withers, S. H.
  • Mason, R. A.
OrganizationsLocationPeople

article

Photoemission Electron Microscopy of TiO2 Anatase Films Embedded with Rutile Nanocrystals

  • Droubay, Timothy C.
  • Joly, Alan G.
  • Shao, Rui
  • Hess, Wayne P.
  • Xiong, Gang
  • Chambers, Scott A.
  • Beck, Kenneth M.
Abstract

Photoemission electron microscopy (PEEM) excited by x-ray and UV sources is used to investigate epitaxial anatase thin films embedded with rutile nanocrystals, a model system for the study of heterocatalysis on mixed-phase TiO2. Both excitation sources show distinct contrast between the two TiO2 phases, however, the contrast is reversed. Rutile nanocrystals appear darker than the anatase film in X-ray PEEM images but brighter in UV-PEEM images. Topography-induced contrast is dominant X-ray PEEM imaging, whereas work function contrast, dominates for UV-PEEM. Work function contrast results from the differences in work function and surface defect state densities between the two phases near the Fermi level. This assertion is confirmed by UPS data that shows the rutile work function to be 0.2 eV lower and a greater occupied valence band density-of-states in rutile (100) than in anatase (001). Since the boundaries between rutile nanocrystals and the anatase film are clearly resolved, these results indicate that PEEM studies of excited state dynamics and heterocatalysis are possible at chemically intriguing mixed-phase TiO2 interfaces and grain boundaries.

Topics
  • density
  • impedance spectroscopy
  • surface
  • grain
  • phase
  • thin film
  • defect
  • electron microscopy
  • ultraviolet photoelectron spectroscopy