Detail publikace

Near-field study of hot spot photoluminescence decay in ZnS:Mn nanoparticles

Originální název

Near-field study of hot spot photoluminescence decay in ZnS:Mn nanoparticles

Anglický název

Near-field study of hot spot photoluminescence decay in ZnS:Mn nanoparticles

Jazyk

en

Originální abstrakt

The local spatial distribution of photoluminescence due to the creation of hot luminescence centers was measured in the optical near field by Scanning near field optical microscope at emission peaks of materials (lambda 595nm), which is due to the luminescence of Mn2plus in ZnS. The excitation bandgap of ZnS forms exitons, and these excitons get the center of Mn2plus through nonradiation dominates, by means of transition of 4T1 to 6A1 luminescence. This spectrum is evidence that Mn2plus has been incorporated into the ZnS nanoparticles. In comparison with the bulk ZnSMn phosphors these nanoparticles have clearly higher luminescent efficiency with its luminescent decay time at least 4 orders of magnitude slower. It means that the oscillator intensity of luminescent centers in ZnS-Mn nanocrystal enhances at least 4 orders of magnitude than that in corresponding bulk ZnSMn.

Anglický abstrakt

The local spatial distribution of photoluminescence due to the creation of hot luminescence centers was measured in the optical near field by Scanning near field optical microscope at emission peaks of materials (lambda 595nm), which is due to the luminescence of Mn2plus in ZnS. The excitation bandgap of ZnS forms exitons, and these excitons get the center of Mn2plus through nonradiation dominates, by means of transition of 4T1 to 6A1 luminescence. This spectrum is evidence that Mn2plus has been incorporated into the ZnS nanoparticles. In comparison with the bulk ZnSMn phosphors these nanoparticles have clearly higher luminescent efficiency with its luminescent decay time at least 4 orders of magnitude slower. It means that the oscillator intensity of luminescent centers in ZnS-Mn nanocrystal enhances at least 4 orders of magnitude than that in corresponding bulk ZnSMn.

BibTex


@article{BUT45105,
  author="Lubomír {Grmela} and Pavel {Tománek} and Pavel {Škarvada}",
  title="Near-field study of hot spot photoluminescence decay in ZnS:Mn nanoparticles",
  annote="The local spatial distribution of photoluminescence due to the creation of hot
luminescence centers was measured in the optical near field by Scanning near field optical
microscope at emission peaks of materials (lambda 595nm), which is due to the luminescence of Mn2plus in
ZnS. The excitation bandgap of ZnS forms exitons, and these excitons get the center of Mn2plus
through nonradiation dominates, by means of transition of 4T1 to 6A1 luminescence. This spectrum is
evidence that Mn2plus has been incorporated into the ZnS nanoparticles. In comparison with the bulk
ZnSMn phosphors these nanoparticles have clearly higher luminescent efficiency with its
luminescent decay time at least 4 orders of magnitude slower. It means that the oscillator intensity
of luminescent centers in ZnS-Mn nanocrystal enhances at least 4 orders of magnitude than that in
corresponding bulk ZnSMn.",
  address="TransTech Publication",
  chapter="45105",
  institution="TransTech Publication",
  journal="Materials Science Forum",
  number="567",
  volume="2007",
  year="2007",
  month="december",
  pages="241--244",
  publisher="TransTech Publication",
  type="journal article in Web of Science"
}