2019
DOI: 10.1016/j.jlumin.2019.04.017
|View full text |Cite
|
Sign up to set email alerts
|

A single-phase NaCa2Mg2V3O12:Sm3+ phosphor: Synthesis, energy transfer, and luminescence properties

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
5
0

Year Published

2019
2019
2023
2023

Publication Types

Select...
7

Relationship

0
7

Authors

Journals

citations
Cited by 62 publications
(5 citation statements)
references
References 30 publications
0
5
0
Order By: Relevance
“…When exciting the host at 345 nm (absorption maximum), a broad emission (400–700 nm) band peaking at about 511 nm exhibit luminescence in the bluish–green region. According to the earlier reports, this bluish–green luminescence of vanadate‐based systems might be attributed to ligand (2p of O 2− ) to metal (3d of V 5+ ) charge transfer bands localized within the tetrahedrally coordinated (VO 4 ) 3− groups 36 …”
Section: Resultsmentioning
confidence: 77%
See 1 more Smart Citation
“…When exciting the host at 345 nm (absorption maximum), a broad emission (400–700 nm) band peaking at about 511 nm exhibit luminescence in the bluish–green region. According to the earlier reports, this bluish–green luminescence of vanadate‐based systems might be attributed to ligand (2p of O 2− ) to metal (3d of V 5+ ) charge transfer bands localized within the tetrahedrally coordinated (VO 4 ) 3− groups 36 …”
Section: Resultsmentioning
confidence: 77%
“…According to the earlier reports, this bluish-green luminescence of vanadate-based systems might be attributed to ligand (2p of O 2− ) to metal (3d of V 5+ ) charge transfer bands localized within the tetrahedrally coordinated (VO 4 ) 3− groups. 36 Figure 7 depicts the excitation spectra (λ emi = 610 nm) of the host CLMV and the Eu 3+ ions doped at different concentrations (x = 0.00-0.09 mol) in the CLMV phosphors. As can be seen, the strong broad excitation band (for x = 0.01-0.09 mol) spanning from 220 to 400 nm might be attributed to the overlap of the transitions of (VO 4 ) 3− groups and form the charge transfer of O 2− to Eu 3+ (250 to 280 nm).…”
Section: Photoluminescence Studiesmentioning
confidence: 99%
“…Therefore the diffraction angle θ should be lower to keep the italicnλ value constant. [ 18 ] To obtain confirmation of the substitution of the Eu 3+ ion for the Y 3+ ion, an acceptable percentage difference D r was calculated using the following Equation (1): [ 19 ] Drgoodbreak=Rs()CNRd()CNRs()CNgoodbreak×100% where R s and R d represent the ionic radii of substituted host ion Y 3+ and dopant ion Eu 3+ in the crystal lattice. It has been reported that to obtain the ideal substitution of doping ion in a crystal structure, the value of D r should not exceed 30%.…”
Section: Resultsmentioning
confidence: 99%
“…Therefore the diffraction angle θ should be lower to keep the nλ value constant. [18] To obtain confirmation of the substitution of the Eu 3+ ion for the Y 3+ ion, an acceptable percentage difference D r was calculated using the following Equation ( 1): [19] D…”
Section: Characterizationmentioning
confidence: 99%
“…12,13 So far, several garnet structured vanadates, such as LiCa 3 ZnV 3 O 12 , 14 NaCa 2 Mg 2 V 3 O 12 , 15,16 Ca 2 KZn 2 (VO 4 ) 3 , 17 and KCa 2 Mg 2 V 3 O 12 , 18 have been reported for the self-activating luminescent emissions. To expand the luminescent property of the garnet-structured vanadate phosphors, various rare earth ions have been introduced into these hosts, resulting in several new luminescent systems, such as NaCa 2 Mg 2 V 3 O 12 :Sm 3+ , 19 Ca 2 AgZn 2 V 3 O 12 :Nb 5+ , 20 CaZnV 2 O 7 :-Eu 3+ , 21 and Ca 2 KZn 2 V 3 O 12 :Dy 3+ . 22 Several questions should be discussed as the rare earth ions with characteristic luminescence being doped into hosts with self-activating emissions.…”
Section: Introductionmentioning
confidence: 99%