Luminescence properties of green emission of SiO2/Zn2SiO4:Mn nanocomposite prepared by sol–gel method
Green light emitting Mn2+ doped Zn2SiO4 particles embedded in SiO2 host matrix were synthesized by a sol–gel method. After the incorporation of ZnO:Mn nanoparticles in a silica monolith using sol–gel method with supercritical drying of ethyl alcohol in two steps, it was heat treated in air at 1200°C...
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Veröffentlicht in: | Physica. E, Low-dimensional systems & nanostructures Low-dimensional systems & nanostructures, 2013-09, Vol.53, p.48-54 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Green light emitting Mn2+ doped Zn2SiO4 particles embedded in SiO2 host matrix were synthesized by a sol–gel method. After the incorporation of ZnO:Mn nanoparticles in a silica monolith using sol–gel method with supercritical drying of ethyl alcohol in two steps, it was heat treated in air at 1200°C for 2h in order to obtain the SiO2/α-Zn2SiO4:Mn nanocomposites. The microstructure of phosphor crystals was characterized by transmission electron microscopy (TEM) and X-ray diffraction (XRD). XRD results indicate that the pure phase α-Zn2SiO4 with rhombohedral structure was obtained after thermal treatment at 1200°C. The SiO2/α-Zn2SiO4:Mn nanocomposites with a Mn doping concentration of 1.5at% exhibit two broadband emissions in the visible range: a strong green emission at around 525nm and a second one in the range between 560 and 608nm. This nanocomposite with a Mn doping concentration of 0.05 shows the highest relative emission intensity. Upon 255nm excitation, the luminescence decay time of the green emission of Zn2SiO4:Mn around 525nm is 11ms. The luminescence spectra at 525nm (4T1–6A1) and lifetime of the excited state of Mn2+ ions-doped Zn2SiO4 nanocrystals are investigated.
•Elaboration of Mn doped Zn2SiO4 nanoparticles.•Structural and optical characterizations of Zn2SiO4:Mn nanoparticles.•The powder shows an average particle size of 25nm.•A strong luminescence band in the visible region. |
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ISSN: | 1386-9477 1873-1759 |
DOI: | 10.1016/j.physe.2013.04.020 |