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 (2/2 displayed)

  • 2023Transformation kinetics for low temperature post-deposition crystallization of TiO 2 thin films prepared via atomic layer deposition (ALD) from tetrakis(dimethylamino)titanium(IV) (TDMAT) and water3citations
  • 2017The Effect of Low Temperature Annealing on the Deactivation and Defect Formation in Highly Doped Si:P Epitaxially Grown Filmscitations

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Chart of shared publication
Losego, Mark
1 / 2 shared
Gregory, Shawn
1 / 1 shared
Freychet, Guillaume
1 / 8 shared
Wooding, Jamie
1 / 1 shared
Kalaitzidou, Kyriaki
1 / 2 shared
Li, Xuebin
1 / 1 shared
Weinrich, Zach
1 / 1 shared
Sharma, Shashank
1 / 2 shared
Brown, David Lee
1 / 1 shared
Jones, Kevin Scott
1 / 1 shared
Chung, Hua
1 / 1 shared
Chart of publication period
2023
2017

Co-Authors (by relevance)

  • Losego, Mark
  • Gregory, Shawn
  • Freychet, Guillaume
  • Wooding, Jamie
  • Kalaitzidou, Kyriaki
  • Li, Xuebin
  • Weinrich, Zach
  • Sharma, Shashank
  • Brown, David Lee
  • Jones, Kevin Scott
  • Chung, Hua
OrganizationsLocationPeople

article

Transformation kinetics for low temperature post-deposition crystallization of TiO 2 thin films prepared via atomic layer deposition (ALD) from tetrakis(dimethylamino)titanium(IV) (TDMAT) and water

  • Losego, Mark
  • Gregory, Shawn
  • Freychet, Guillaume
  • Atassi, Amalie
  • Wooding, Jamie
  • Kalaitzidou, Kyriaki
Abstract

Background: We report on the fundamental crystallization kinetics of atomic layer deposited (ALD) TiO2 thin films undergoing a post-deposition anneal (PDA) at low temperatures to probe differences in the as-deposited film microstructure. Methods: The system of study is ALD TiO2 thin films prepared from tetrakis(dimethylamino)titanium(IV) (TDMAT) and water at 120 °C, 140 °C and 160 °C followed by ex situ low temperature annealing at temperatures ranging from 140 °C to 220 °C. All as-deposited TiO2 thin films are amorphous by X-ray diffraction (XRD). Post-deposition annealing (PDA) produces large grain anatase crystals, confirmed by XRD and top-view scanning electron microscopy (SEM). A detailed SEM study is performed to quantify the nucleation and growth kinetics by fitting microstructural data to the Johnson-Mehl-Avrami-Kolmogorov (JMAK) equation. Finally, a time-temperature-transformation (TTT) diagram is constructed to summarize the differences in crystallization behavior at different ALD deposition temperatures. Results and conclusions: Fitting microstructural data to the JMAK equation reveals an Avrami exponent close to 3 with continuous nucleation, suggesting two-dimensional, plate-like crystal growth. Applying an Arrhenius relationship to the phase transformation data, the combined activation energy for nucleation and growth is found to be 1.40–1.58 eV atom-1. Nucleation rates are determined, and an Arrhenius relationship is used to calculate the critical Gibbs free energy for nucleation (~1.3–1.4 eV atom-1). As such, nucleation is the rate-limiting step for the amorphous to anatase phase transformation. ALD growth temperature is found to dictate film microstructure with lower deposition temperatures reducing the nucleation rate and leading to larger grain sizes irrespective of PDA conditions. The nucleation rate pre-exponential frequency factor increases with increasing deposition temperature, thereby increasing the likelihood for nucleation. Interestingly, it is this difference in the vibrational modes ...

Topics
  • impedance spectroscopy
  • amorphous
  • grain
  • grain size
  • phase
  • scanning electron microscopy
  • x-ray diffraction
  • thin film
  • titanium
  • two-dimensional
  • annealing
  • activation
  • crystallization
  • atomic layer deposition