2013
DOI: 10.1016/j.jlumin.2012.07.021
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Co-precipitation synthesis and photoluminescence properties of Ba1−xMoO4:xEu3+ red phosphors

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Cited by 41 publications
(17 citation statements)
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“…The conventional solution is adding a red-emitting phosphor to the unit of the white LEDs. In this approach, most red phosphors, for example Y 2 O 2 S:Eu 3+ , CaS:Eu 2+ and SrS:Eu 2+ , are based on sulfides which are chemically unstable and inefficient [5,6]. Therefore, exploring novel red phosphors to overcome the above disadvantages is very necessary.…”
Section: Introductionmentioning
confidence: 99%
“…The conventional solution is adding a red-emitting phosphor to the unit of the white LEDs. In this approach, most red phosphors, for example Y 2 O 2 S:Eu 3+ , CaS:Eu 2+ and SrS:Eu 2+ , are based on sulfides which are chemically unstable and inefficient [5,6]. Therefore, exploring novel red phosphors to overcome the above disadvantages is very necessary.…”
Section: Introductionmentioning
confidence: 99%
“…Fig. 7(a), a strong broad band from 220 nm to 340 nm is assigned to the combination of the charge transfer band (CTB) transition of O 2 À -Mo 6 þ and O 2 À -Eu 3 þ groups [17,23,27]. For CaMoO 4 :yEu 3 þ , when the Eu 3 þ concentration is increased to 0.08 or 0.20, the absorption intensity of the samples becomes weaker because the concentration quenching occurs.…”
Section: Resultsmentioning
confidence: 99%
“…Mo ions are the central metal ion and coordinated by four O 2À ions, leading to that the structure is very stable [20][21][22]. Feng et al [23] and Xu Li et al [24] had analyzed the luminescent properties of Ba 1À x MoO 4 :xEu 3 þ and SrMoO 4 :Dy 3 þ phosphors, respectively. Fa-bin Cao et [25] and Ca 0.54 Sr 0.34-1.5x Eu 0.08 Sm x (MoO 4 ) y (WO4) 1À y [26] had the high-efficiency red light emission under 395 nm excitation.…”
Section: Introductionmentioning
confidence: 99%
“…Some strong narrow peaks are observed between 360 and 500 nm and are attributed to the 4f-4f transitions of the Eu 3+ ion. On the other hand, the CT band of Eu 3+ -O 2− is not clearly observed in the excitation spectra, possibly due to the overlap of the CT band with that of the molybdate group [15], [17]- [19]. In the emission spectra, all peaks corresponded to the Eu 3+ 4f-4f transition.…”
Section: Methodsmentioning
confidence: 98%