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Title: Eu3+-doped wide band gap Zn2SnO4 semiconductor nanoparticles: Structure and luminescence

Journal Article · · Journal of Physical Chemistry. C
 [1];  [2];  [3];  [4];  [2];  [2];  [4];  [2]
  1. National Institute of Standards and Technology, Gaithersburg, MD (United States); National Renewable Energy Lab. (NREL), Golden, CO (United States); Catalonia Institute for Energy Research (IREC), Barcelona (Spain)
  2. Univ. of Novi Sad, Novi Sad (Serbia)
  3. Univ. of Houston, Houston, TX (United States)
  4. Catalonia Institute for Energy Research (IREC), Barcelona (Spain)

Nanocrystalline Zn2SnO4 powders doped with Eu3+ ions were synthesized via a mechanochemical solid-state reaction method followed by postannealing in air at 1200 °C. X-ray diffraction (XRD), energy-dispersive X-ray (EDX), and Raman and photoluminescence (PL) spectroscopies provide convincing evidence for the incorporation of Eu3+ ions into the host matrix on noncentrosymmetric sites of the cubic inverse spinel lattice. Microstructural analysis shows that the crystalline grain size decreases with the addition of Eu3+. Formation of a nanocrystalline Eu2Sn2O7 secondary phase is also observed. Luminescence spectra of Eu3+-doped samples show several emissions, including narrow-band magnetic dipole emission at 595 nm and electric dipole emission at 615 nm of the Eu3+ ions. Excitation spectra and lifetime measurements suggest that Eu3+ ions are incorporated at only one symmetry site. According to the crystal field theory, it is assumed that Eu3+ ions participate at octahedral sites of Zn2+ or Sn4+ under a weak crystal field, rather than at the tetrahedral sites of Zn2+, because of the high octahedral stabilization energy for Eu3+. Activation of symmetry forbidden (IR-active and silent) modes is observed in the Raman scattering spectra of both pure and doped samples, indicating a disorder of the cation sublattice of Zn2SnO4 nanocrystallites. These results were further supported by the first principle lattice dynamics calculations. The spinel-type Zn2SnO4 shows effectiveness in hosting Eu3+ ions, which could be used as a prospective green/red emitter. As a result, this work also illustrates how sustainable and simple preparation methods could be used for effective engineering of material properties.

Research Organization:
National Renewable Energy Laboratory (NREL), Golden, CO (United States)
Sponsoring Organization:
USDOE Office of Energy Efficiency and Renewable Energy (EERE), Sustainable Transportation Office. Hydrogen Fuel Cell Technologies Office
Grant/Contract Number:
AC36-08GO28308
OSTI ID:
1330001
Report Number(s):
NREL/JA-5900-67318
Journal Information:
Journal of Physical Chemistry. C, Vol. 120, Issue 33; ISSN 1932-7447
Publisher:
American Chemical SocietyCopyright Statement
Country of Publication:
United States
Language:
English
Citation Metrics:
Cited by: 38 works
Citation information provided by
Web of Science

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Boosting the photovoltaic performance of Zn 2 SnO 4 -based dye-sensitized solar cells by Si doping into Zn 2 SnO 4 journal July 2017
Effects of the Concentration of Eu3+ Ions and Synthesizing Temperature on the Luminescence Properties of Sr2−xEuxZnMoO6 Phosphors journal December 2016
Hydrothermal growth of Zn 2 SnO 4 :Eu,Ca for red emission journal March 2018
Structural and spectroscopic investigations on the quenching free luminescence of europium oxalate nanocrystals journal April 2019
Eu2+-Activated Green-Emitting Phosphor Obtained from Eu3+ Ions doping Zeolite-3A in Air Surroundings and Its Efficient Green Light-Emitting Diodes journal August 2019
Morphological zinc stannate: synthesis, fundamental properties and applications journal January 2017
Effect of Eu 2 O 3 Concentration on the Properties of Red-Light-Emitting Sr1.5Ca0.5SiO 4 Fluorescent Materials journal September 2019
Structural and spectroscopic investigations on the quenching free luminescence of europium oxalate nanocrystals text January 2019
Structural and spectroscopic investigations on the quenching free luminescence of europium oxalate nanocrystals text January 2019