2002
DOI: 10.1016/s0022-2313(02)00350-2
|View full text |Cite
|
Sign up to set email alerts
|

Luminescence of nanocrystalline ZnS:Cu2+

Abstract: Temperature dependent luminescence and luminescence lifetime measurements are reported for nanocrystalline ZnS:Cu 2+ particles. Based on the variation of the emission wavelength as a function of particle size (between 3.1 and 7.4 nm) and the low quenching temperature (T q ¼ 135 K), the green emission band is assigned to recombination of an electron in a shallow trap and Cu 2+ . The reduction in lifetime of the green emission (from 20 ms at 4 K to 0.5 ms at 300 K) follows the temperature quenching of the emissi… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1

Citation Types

11
108
3

Year Published

2004
2004
2023
2023

Publication Types

Select...
7
1
1

Relationship

0
9

Authors

Journals

citations
Cited by 192 publications
(122 citation statements)
references
References 20 publications
11
108
3
Order By: Relevance
“…Increasing Cu concentration can push the t 2 level of Cu 2+ ions farther away from the valence band; therefore, the emission was significantly quenched when the dopant ion concentration reached over 2 at % against the ZnS host. In a particular case, red-orange light emission from the ZnS:Cu nanocrystal was reported by Bol et al; 33 however, we did not observe this phenomenon with our ZnS:Cu-MPA nanocrystal.…”
Section: Resultscontrasting
confidence: 61%
“…Increasing Cu concentration can push the t 2 level of Cu 2+ ions farther away from the valence band; therefore, the emission was significantly quenched when the dopant ion concentration reached over 2 at % against the ZnS host. In a particular case, red-orange light emission from the ZnS:Cu nanocrystal was reported by Bol et al; 33 however, we did not observe this phenomenon with our ZnS:Cu-MPA nanocrystal.…”
Section: Resultscontrasting
confidence: 61%
“…This can only be possible if Pb 2+ ions are selectively excited. Note that blue, green and red emissions from Pb 2+ have been reported and the red emission, similar to the one in figure 20, was attributed to 3 P 0,1 → 1 S 0 transition of Pb 2+ (Bol and Meijerink, 2001). As shown in the inset of figure 20, the red-orange cathodoluminescence degraded by more than 50% following the prolonged irradiation by 2 keV electrons.…”
Section: Sio 2 :Pbssupporting
confidence: 75%
“…Therefore the orangered emission in figure 20 is neither coming from SiO 2 nor PbS nanoparticles. This emission is similar to emission associated with transitions in Pb 2+ ions in ZnS:Pb 2+ (Bol and Meijerink, 2001) and SiO 2 :Pb 2+ (Ntwaeaborwa et al, 2009b). Although the exact mechamism of this emission is not known yet, it is reasonable to attribute the emission to transisions in Pb 2+ .…”
Section: Sio 2 :Pbssupporting
confidence: 66%
“…The grown crystals are belongs to high band gap materials category which makes them favorable applicant for optoelectronic device applications [38,[50][51][52]. and another violet-blue emission band at *420 nm (broad), which may be attributed to creation of S 2-vacancies due to dye doping as a results of vacancy sites and defect concentrations [53][54][55]. It is interesting to be noted here that the PL intensity of UV emission has been remarkably enhanced, which may be due to increase in vacancy related defects (F-centers) in the doped crystals that acts as color centers.…”
Section: Diffuse Reflectance (Dr) Analysismentioning
confidence: 99%