2018
DOI: 10.1016/j.physb.2017.07.042
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Energy transfer from Pr 3+ to Gd 3+ ions in BaB 8 O 13 phosphor for phototherapy lamps

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Cited by 31 publications
(8 citation statements)
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“…An additional peak was observed at 22.00° that might be due to the doping of RE ions in the host lattice. [ 24–26 ] This increase in intensity after doping with Dy 3+ may be due to an internal change in local crystal structure. [ 27,28 ]…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…An additional peak was observed at 22.00° that might be due to the doping of RE ions in the host lattice. [ 24–26 ] This increase in intensity after doping with Dy 3+ may be due to an internal change in local crystal structure. [ 27,28 ]…”
Section: Resultsmentioning
confidence: 99%
“…An additional peak was observed at 22.00 that might be due to the doping of RE ions in the host lattice. [24][25][26] This increase in intensity after doping with Dy 3+ may be due to an internal change in local crystal structure. [27,28] It is well known that four main peaks (222), (400), (440), and (622) are characteristic of a defective fluorite structure.…”
Section: Phase and Crystal Analysismentioning
confidence: 99%
“…From Figure , a spectral overlap between the emission spectrum of Ce 3+ and the excitation spectrum of Tb 3+ can be seen. The prime condition for the energy transfer to take place is that there should be a spectral overlap between the emission and excitation spectra of sensitizers and activators, respectively . The Ce 3+ ions when excited by 279 nm emits in the broad band ranging from 300 to 400 nm, which is the excitation region for Tb 3+ ions as shown in Figure .…”
Section: Resultsmentioning
confidence: 99%
“…The UV-B band at 313 nm is very typical of the Gd 3+ ions and it's related to transitions corresponding to the 6 P7/2 → 8 S7/2 energy states [12] as depicted on Figure 4b. This type of radiation is known to be effective for treating skin diseases such as vitiligo vulgaris, psoriasis, and periodontitis [13][14][15][16][17][18]. The red emission peak at 628 nm can be attributed to the 6 G7/2 → 6 P3/2 transition as the excitation energy of 5.39 eV should be enough for the excited electron to reach the conduction band of the host material where the 6 Gj energy state of Gd 3+ is located [19].…”
Section: Optical Propertiesmentioning
confidence: 99%