2003
DOI: 10.1016/s0022-4596(02)00126-3
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Visible and near-IR luminescence via energy transfer in rare earth doped mesoporous titania thin films with nanocrystalline walls

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Cited by 226 publications
(182 citation statements)
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References 38 publications
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“…Annealed sample shows a strong and sharp PL peaks at 400 nm, 452 nm in the PL Spectrum as shown in Fig.4. It is found that PL intensity increased gradually after annealing at 800 o C. The emission peaks at 400 nm (3.1 eV) was due to main band transition and Er related trapped states was attributed for emission [35,36,38] at 452 nm (~2.74 eV) [37][38][39][40][41] which has a good agreement with the value calculated from optical absorption measurement. …”
Section: Optical Absorption Analysissupporting
confidence: 69%
See 1 more Smart Citation
“…Annealed sample shows a strong and sharp PL peaks at 400 nm, 452 nm in the PL Spectrum as shown in Fig.4. It is found that PL intensity increased gradually after annealing at 800 o C. The emission peaks at 400 nm (3.1 eV) was due to main band transition and Er related trapped states was attributed for emission [35,36,38] at 452 nm (~2.74 eV) [37][38][39][40][41] which has a good agreement with the value calculated from optical absorption measurement. …”
Section: Optical Absorption Analysissupporting
confidence: 69%
“…The optical band gap value close to ~ 3.3 eV (375 nm) and ~3.1 eV (400) was responsible for the TiO 2 main band transition for the as deposited and the 800 0 C annealed sample respectively. The band gap value ~ 2.76 eV was attributed to the Er related trapped states [35][36][37][38][39][40][41]. So, these results reveal that the doping of erbium oxide (Er 2 O 3 ) created a small red shift of 0.2 eV on the band gap value of the host material due to the formation of T-O-Er bond when annealed at 800 o C. Figure 4 shows the PL spectrum of Er 2 O 3 NP decorated TiO 2 NW at an excitation wavelength of 250 nm using F-7000 FL spectrophotometer.…”
Section: Optical Absorption Analysismentioning
confidence: 99%
“…The origins of these emissions are attributed to the corresponding RE ions as the spectral positions and shapes agree with those reported previously but with different hosts. (23)(24)(25)(26)(27)(28)(29)(30)(31)(32) The Ce-, Gd-, and Yb-doped samples did not show any measurable signals. These results can be interpreted as follows.…”
Section: Methodsmentioning
confidence: 99%
“…The origins of these emission lines were attributed to each trivalent RE ion based on previous studies. (23)(24)(25)(26)(27)(28)(29)(30)(31)(32)34,35) The Ce-doped sample showed no measurable PL emission. Unlike PL, the Gd-doped sample showed a sharp emission line at 310 nm due to the 4f-4f transition of Gd…”
Section: Methodsmentioning
confidence: 99%
“…5). As has been proposed by Stucky et al 10 The study has been supported by CREST of Japan Science and Technology Agency (JST). …”
mentioning
confidence: 92%