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Characterization of Photoluminescent (Y 1– x Eu x ) 2 O 3 Thin Films Prepared by Metallorganic Chemical Vapor Deposition
Author(s) -
McKittrick Joanna,
Bacalski Carlos F.,
Hirata G. A.,
Hubbard Kevin M.,
Pattillo S. G.,
Salazar Kenneth V.,
Trkula M.
Publication year - 2000
Publication title -
journal of the american ceramic society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.9
H-Index - 196
eISSN - 1551-2916
pISSN - 0002-7820
DOI - 10.1111/j.1151-2916.2000.tb01361.x
Subject(s) - photoluminescence , materials science , metalorganic vapour phase epitaxy , thin film , chemical vapor deposition , nanocrystalline material , analytical chemistry (journal) , europium , crystallite , annealing (glass) , mineralogy , epitaxy , luminescence , nanotechnology , chemistry , metallurgy , optoelectronics , layer (electronics) , chromatography
The purpose of this study was to identify and correlate the microstructural and luminescence properties of europium‐doped Y 2 O 3 (Y 1– x Eu x ) 2 O 3 thin films deposited by metallorganic chemical vapor deposition (MOCVD), as a function of deposition time and temperature. The influence of deposition parameters on the crystallite size and microstructural morphology were examined, as well as the influence of these parameters on the photoluminescence emission spectra. (Y 1– x Eu x ) 2 O 3 thin films were deposited onto (111) silicon and (001) sapphire substrates by MOCVD. The films were grown by reacting yttrium and europium tris(2,2,6,6‐tetramethyl–3,5‐heptanedionate) precursors with an oxygen atmosphere at low pressures (5 torr (1.7 × 10 3 Pa)) and low substrate temperatures (500°–700°C). The films deposited at 500°C were smooth and composed of nanocrystalline regions of cubic Y 2 O 3 , grown in a textured [100] or [110] orientation to the substrate surface. Films deposited at 600°C developed, with increasing deposition time, from a flat, nanocrystalline morphology into a platelike growth morphology with [111] orientation. Monoclinic (Y 1– x Eu x ) 2 O 3 was observed in the photoluminescence emission spectra for all deposition temperatures. The increase in photoluminescence emission intensity with increasing postdeposition annealing temperature was attributed to the surface/grain boundary area‐reduction effect.