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  • 1
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 89 (2001), S. 4491-4496 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Spectroscopic ellipsometry (SE) was used to characterize the sol–gel derived (K0.5Na0.5)0.4(Sr0.6Ba0.4)0.8Nb2O6 (KNSBN) thin films as a function of sol concentration. In the analysis of the measured SE spectra, a modified double-layer Forouhi–Bloomer model was adopted to represent the optical properties of the KNSBN films. In this model, the films were assumed to consist of two layers—a bottom bulk KNSBN layer and a surface layer that composed of bulk KNSBN as well as void. Good agreement was obtained between the measured spectra and the model calculations in the chosen spectral region. Effective medium approximation theory was used to evaluate the effective refractive index for the surface layer. The results of SE have been correlated with atomic force microscopy measurements of surface roughness. Our analyses have shown that the surface layer had a lower refractive index than the bottom one. In addition, the refractive index and the surface roughness of the KNSBN films increase with the sol concentration. © 2001 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 91 (2002), S. 1871-1874 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Spectral properties of blue upconversion luminescences in Tm3+ doped tellurite (PWT, PbF2-WO3-TeO2) glasses and germanate (PWG, PbF2-WO3-GeO2) glasses pumped by a tunable dye laser were studied at room temperature. Two emission bands centered at 453 and 477 nm, corresponding to the 1D2→3H4 and 1G4→3H6 transitions of Tm3+ ions respectively, were observed. The two-photon absorption mechanism responsible for the 477 nm luminescence was confirmed by a quadratic dependence of luminescent intensities on the excitation power. Tellurite glasses showed a weaker upconversion luminescence than germanate glasses. This observation was inconsistent with the prediction from the phonon sideband measurement. In this article, Raman spectroscopy and transmittance measurement were employed to investigate the origin of the difference in upconversion luminescences in the two glasses. Compared with phonon sideband spectroscopy, Raman spectroscopy extracts more information, including both phonon energy and phonon density, and therefore, is a more effective analytical tool for understanding upconversion luminescence. Our results showed that the phonon energy as well as phonon density of the host glass is important in determining the upconversion efficiency. © 2002 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Woodbury, NY : American Institute of Physics (AIP)
    Applied Physics Letters 79 (2001), S. 4310-4312 
    ISSN: 1077-3118
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Optically transparent nanocomposites of strontium–barium–niobate (SBN) and silica were fabricated via a novel sol–gel method. The nanocomposites were annealed in temperatures of 600–800 °C to yield the nanometer-sized tetragonal tungsten–bronze phase of SBN crystallites. Photoluminescence studies at temperatures from 10 K to room temperature were performed. The undoped silica matrix showed a strong emission band at 3.2 eV and a weak emission band at 2.65 eV. They were noticeably suppressed in our SBN/SiO2 nanocomposites. Extra sharp peaks on top of the 3.2 eV band were seen. An additional emission band at 2.3 eV due to transitions within the NbO6 complex of SBN crystallites was also observed. This emission band showed a large blueshift with decreasing SBN crystallite size. This demonstrates that the photoluminescence spectra of ferroelectric-doped silica nanocomposites have a strong dependence on crystallite size. © 2001 American Institute of Physics.
    Type of Medium: Electronic Resource
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