2008
DOI: 10.1016/j.mseb.2007.07.056
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Luminescence of TiO2:Pr nanoparticles incorporated in silica aerogel

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Cited by 27 publications
(15 citation statements)
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“…3 E CT was chosen 3.8 eV, see arrow 2). Kaczkan et al 22 does not observe any Pr 3+ 4f-4f emission, and Amlouk et al 23 show that the emission from the 3 P 0 level to 3 H 6 and 3 F 4 (arrow 3) in 20-30 nm sized TiO 2 starts to quench above 70K. Such low quenching temperature implies that the 3 P 0 level is located close below E X ; in Fig.…”
Section: Methodsmentioning
confidence: 87%
“…3 E CT was chosen 3.8 eV, see arrow 2). Kaczkan et al 22 does not observe any Pr 3+ 4f-4f emission, and Amlouk et al 23 show that the emission from the 3 P 0 level to 3 H 6 and 3 F 4 (arrow 3) in 20-30 nm sized TiO 2 starts to quench above 70K. Such low quenching temperature implies that the 3 P 0 level is located close below E X ; in Fig.…”
Section: Methodsmentioning
confidence: 87%
“…The PL spectra, a strong red emission band centered at 643 nm is observed from all samples, is induced by 449 nm excitation. The strong sharp emission peak around 643 nm is attributed to 3 P 0 → 3 F 2 transition, while the weak red emission located at around 616 nm is owing to 3 P 0 → 3 H 6 transition, which is induced by the lack of inversion symmetry at the Pr 3+ ions sites [12]. The Pr 3+ -related narrow band emission at about 643 nm corresponding to the intense absorption of 449 nm suggests an effective host-to-activator energy transfer.…”
Section: Resultsmentioning
confidence: 99%
“…For the TiO 2 sputtering times longer than 12 min only an orange emission at 650 nm is observed and its intensity increases as the TiO 2 -shell layer thickness increases further. As regards the emission band at 650 nm, there are two reports: one is on that of ZnS [8] and the other on that of Pr 3 + -doped TiO 2 incorporated in silica matrix [24], yet the orange emission in our nanowire samples seems to have an origin different from either of the two. The rapid increase in the emission intensity with an increase in the TiO 2 -shell layer thickness suggests that the emission at 650 nm does not originate from deep levels in the ZnS cores but from the deep levels like Zn and S dopants generated in the TiO 2 shells by annealing.…”
Section: Resultsmentioning
confidence: 69%
“…Besides these, an orange emission band centered at 650 nm has been reported for Pr 3 + -doped TiO 2 incorporated in silica matrix [24]. The violet emission is known to be attributed to self-trapped excitons localized on TiO 6 octahedra [14,15], while the blue emission originates from oxygen (O) vacancies [15,16] or surface states [17,18].…”
Section: Introductionmentioning
confidence: 97%
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