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Correlation between Cr3+ Luminescence and Oxygen Vacancy Disorder in Strontium Titanate under MeV Ion Irradiation

Journal Article · · Journal of Physical Chemistry. C
 [1];  [2];  [3];  [4];  [5]
  1. Univ. of Tennessee, Knoxville, TN (United States)
  2. Univ. of Tennessee, Knoxville, TN (United States); Missouri Univ. of Science and Technology, Rolla, MO (United States)
  3. Centro de Microanalisis de Materiales, Madrid (Spain)
  4. Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States)
  5. Univ. of Tennessee, Knoxville, TN (United States); Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States)
Strontium titanate (SrTiO3), a model system with a strongly correlated electronic structure, has attracted much attention recently because of its outstanding physicochemical properties and considerable potentials for technological applications. The capability to control oxygen vacancy profiles and their effect on valence states of cations will increase significantly the functionality of devices based on transition metal oxides. This work presents new insights into the near-infrared luminescence emission of Cr3+ centers in stoichiometric SrTiO3 induced using 3 MeV protons at temperatures of 100 K, 170 K, and room temperature. The study covers a wide spectral range, including near-infrared, visible, and near-UV regions. Our main purpose is to investigate the role of the oxygen vacancies introduced by energetic charged particles on the shape and yield of induced luminescence spectra, in particular to explore the interplay between the Cr3+ luminescence at 1.55 eV and oxygen disorder. A clear correlation is found between the decay of the Cr luminescence yield during irradiation and the growth of a band at 2.0 eV, well-resolved below 170 K, which has been very recently attributed to d–d transitions of electrons self-trapped as Ti3+ in the close vicinity of oxygen vacancies. This correlation suggests irradiation-induced oxidation of the Cr3+ (Cr3+ → Crn+, n > 3) via trapping of irradiation-induced holes, while the partner electrons are self-trapped as Ti3+. Here, these new results provide effective guidelines for further understanding the electronic and photocatalytic behavior of STO:Cr3+.
Research Organization:
Oak Ridge National Laboratory (ORNL), Oak Ridge, TN (United States)
Sponsoring Organization:
USDOE Office of Science (SC), Basic Energy Sciences (BES). Materials Sciences & Engineering Division
Grant/Contract Number:
AC05-00OR22725
OSTI ID:
1394589
Journal Information:
Journal of Physical Chemistry. C, Journal Name: Journal of Physical Chemistry. C Journal Issue: 36 Vol. 121; ISSN 1932-7447
Publisher:
American Chemical SocietyCopyright Statement
Country of Publication:
United States
Language:
English

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