0000000000007224
AUTHOR
Witold ŁOjkowski
Luminescence of oxygen related defects in zirconia nanocrystals
The luminescence of undoped tetragonal structure ZrO2 nanocrystals was studied. The luminescence intensity depends on oxygen content in gases mixture in which the nanocrystals were annealed. The distorted Zr-O bond is suggested to be the recombination center for band carriers. The oxygen deficient defect is proposed to be responsible for photoluminescence. (© 2007 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim)
Time-Resolved Luminescence Characteristics of Cerium Doped YAG Nanocrystals
Time-resolved luminescence characteristics have been studied for cerium doped YAG nanopowders (NP) and nanostructured ceramics (NC). The results obtained have been compared to the luminescence characteristics for the well studied YAG:Ce3+ single crystal (SC). It was detected that the luminescence decay kinetics of Ce3+ related emission in nanocrystals can be closely approximated by two exponents, whereas a single exponential decay was observed in the single crystal. It was also found that the luminescence decay time and light yield of Ce3+ emission are strongly dependent on the cerium concentration and an unusual concentration quenching of Ce3+ emission was observed in YAG nanocrystals. The…
Zirconia Based Nanomaterials for Oxygen Sensors – Generation, Characterisation and Optical Properties
Microwave driven hydrothermal synthesis and hydrothermal synthesis were used to obtain ZrO2 nanopowders. Their production with varying phase composition, the characterisation and selected optical properties concerning their potential use as luminescence oxygen sensors are reported. It was found that the powders obtained by the microwave driven hydrothermal method and annealed at 750 0C in air show experiment repeatability within an accuracy of 6 %.
Abstracts from the Fourth International Meeting of ISEV, ISEV2015, Washington, D.C., USA, 23-26 April 2015
Excitonic luminescence in ZnO nanopowders and ceramics
Abstract Fast photoluminescence spectra in the spectral region of 3.1–3.45 eV in ZnO and ZnO:Al ceramics were studied at 14 and 300 K. Ceramics with grains smaller than 100 nm were sintered from nanopowders by high pressure (8 GPa) and low temperature (350 °C). Ceramics with grain sizes 1–5 μm were sintered at 1400 °C. It is shown that excitonic luminescence spectra depend on the ceramics grain size, post preparing annealing and doping. The excitonic luminescence decay time was faster than 2 ns and the afterglow at 30 ns was ∼0.05%.
Luminescence and FTIR Spectroscopy of ZnO Nanocrystals
Time-resolved luminescence and Furje Transformation Infrared (FTIR) absorption spectroscopy for ZnO nanocrystals prepared under different chemical reactions using microwave driven hydrothermal process was studied. OH- group stretching vibration frequency is considerably different in nanocrystals studied and in single ZnO crystal. It is shown that fractions of chemicals used in synthesis process could be found in nanopowders. Luminescence at ~2.0 eV (due to defect states in ZnO crystals and nanopowders) was suppressed in nanopowders obtained by urea method.
Luminescence of ZnO nanopowders
Abstract The luminescence of ZnO nanocrystals prepared by different methods was studied under pulsed electron beam excitation. It is shown that the luminescence intensity depends on the nanocrystal sintering conditions and does not depend on the nanocrystal size within the range 10–50 nm. The relative luminescence intensities for the 3.32 eV (free exciton) and ∼3.20 eV (bound exciton) bands showed a dependence on nanocrystal size. The role of the nanocrystal surface in excitonic luminescence is discussed.
Luminescence of ZrO<sub>2</sub> Nanocrystals
The luminescence of nanocrystalline tetragonal and cubic ZrO2 has been investigated. The tetragonal undoped ZrO2 revealed two luminescence bands, at ~2.0 eV and 2.7 eV , but only one band at ~2.7 eV was observed from cubic ZrO2. This luminescence was shown to be intrinsic. The regular zirconium-oxygen complex excited state is suggested as being responsible for intrinsic luminescence.
The luminescence of ZnO ceramics
Abstract The luminescence properties of ZnO ceramics with grains 100–5000 nm sintered by different techniques from nanopowders were studied. The luminescence decay times were compared with that obtained for ZnO single crystal. The temperature dependence of non-exponential decay of defect luminescence (2.0–2.6 eV) was measured in wide time, intensity and temperature range. The luminescence decay kinetic at T ≤ 20 K shows the decay close to I(t) ∼ t−1 dependence. At temperature region 50–250 K the decay kinetics is more complicate since the TSL was observed in this temperature region. It is shown that the luminescence properties of NP and ceramics strongly depend on defect distribution on gra…