Abstract:The cathodoluminescence (CL) spectra of nanocrystalline Y 2 O 3 :Tb 3+ (0.3%), Y 2 O 3 :Er 3+ (1%), Y 2 O 3 :Tm 3+ (2%) and Y 2 O 3 :Bi 3+ (1%) were recorded in a transmission electron microscope at 200 keV, low current density and various temperatures. The quenching energy of the intrinsic luminescence of the various Y 2 O 3 :Ln 3+ (Ln ¼ Tb, Er and Tm) phosphors was found to be 0.25 eV. The intrinsic luminescence and the strongest spectral transitions of Ln 3+ in these three phosphors exhibit similar temperat… Show more
“…The explanation above on the origin of the 430 nm band in BaAl 2 O 4 :Eu 2+ is an important building block for its mixed luminescence: intrinsic lattice luminescence (F-centre) and Eu 2+ luminescence. This type of mixed luminescence has been described by us in an earlier study on Y 2 O 3 :Ln 3+ (Ln = Eu, Tb, Tm and Er) [53,54].…”
In this article the photoluminescence (PL) and cathodoluminescence (CL) of undoped BaAl 2 O 4 and BaAl 2 O 4 doped with 500 ppm and 3 mol% Eu 2+ is described. The most important results from the CL measurements are: (1) Undoped BaAl 2 O 4 manifested intrinsic CL at 460 nm, which increased at low temperature and did not change significantly upon exposure to the e-beam; (2) Doping BaAl 2 O 4 with Eu 2+ changed the character of the intrinsic luminescence band: it became more sensitive to temperature variations and the band experienced a blue shift to ∼425 nm; (3) electron beam (e-beam) exposure of Ba 0.97 Eu 0.03 Al 2 O 4 at low temperature increased the 425 nm band strongly while the Eu 2+ emission at ∼500 nm decreased by about 70%. The Eu 2+ emission band was symmetric, indicating that BaAl 2 O 4 :Eu has changed to the P6 3 22 phase upon e-beam exposure at low temperature; (4) We have identified the 460 nm band in undoped BaAl 2 O 4 and the 425 nm band in BaAl 2 O 4 :Eu 2+ with F-centre luminescence, corresponding to the F-centre emission in α-Al 2 O 3. The evidence for the assignment of the 425 nm band in BaAl 2 O 4 :Eu 2+ is the spectacular increase of the spectral radiance at 425 nm by e-beam exposure at 200 keV and low temperature. A preliminary model is presented that explains the results. The PL from BaAl 2 O 4 :Eu 2+ quenched at the rather low temperature of 140°C; this observation is explained in terms of thermal ionization of the Eu 2+ ion.
“…The explanation above on the origin of the 430 nm band in BaAl 2 O 4 :Eu 2+ is an important building block for its mixed luminescence: intrinsic lattice luminescence (F-centre) and Eu 2+ luminescence. This type of mixed luminescence has been described by us in an earlier study on Y 2 O 3 :Ln 3+ (Ln = Eu, Tb, Tm and Er) [53,54].…”
In this article the photoluminescence (PL) and cathodoluminescence (CL) of undoped BaAl 2 O 4 and BaAl 2 O 4 doped with 500 ppm and 3 mol% Eu 2+ is described. The most important results from the CL measurements are: (1) Undoped BaAl 2 O 4 manifested intrinsic CL at 460 nm, which increased at low temperature and did not change significantly upon exposure to the e-beam; (2) Doping BaAl 2 O 4 with Eu 2+ changed the character of the intrinsic luminescence band: it became more sensitive to temperature variations and the band experienced a blue shift to ∼425 nm; (3) electron beam (e-beam) exposure of Ba 0.97 Eu 0.03 Al 2 O 4 at low temperature increased the 425 nm band strongly while the Eu 2+ emission at ∼500 nm decreased by about 70%. The Eu 2+ emission band was symmetric, indicating that BaAl 2 O 4 :Eu has changed to the P6 3 22 phase upon e-beam exposure at low temperature; (4) We have identified the 460 nm band in undoped BaAl 2 O 4 and the 425 nm band in BaAl 2 O 4 :Eu 2+ with F-centre luminescence, corresponding to the F-centre emission in α-Al 2 O 3. The evidence for the assignment of the 425 nm band in BaAl 2 O 4 :Eu 2+ is the spectacular increase of the spectral radiance at 425 nm by e-beam exposure at 200 keV and low temperature. A preliminary model is presented that explains the results. The PL from BaAl 2 O 4 :Eu 2+ quenched at the rather low temperature of 140°C; this observation is explained in terms of thermal ionization of the Eu 2+ ion.
“…13). These emission bands are associated with radiative de-excitation of the self-trapped exciton [24,42,43]. Note also that for bulk Y2O3 the exciton emission band is shifted to the high-energy region (3.4-3.5 eV) [41].…”
Section: Optical Absorption and Luminescence: Bandgaps And Excitonic ...mentioning
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.