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  <channel rdf:about="http://hdl.handle.net/123456789/13">
    <title>DSpace Collection: Assistatnt Professor</title>
    <link>http://hdl.handle.net/123456789/13</link>
    <description>Assistatnt Professor</description>
    <items>
      <rdf:Seq>
        <rdf:li rdf:resource="http://hdl.handle.net/123456789/95" />
        <rdf:li rdf:resource="http://hdl.handle.net/123456789/94" />
        <rdf:li rdf:resource="http://hdl.handle.net/123456789/93" />
        <rdf:li rdf:resource="http://hdl.handle.net/123456789/92" />
      </rdf:Seq>
    </items>
    <dc:date>2026-06-05T22:25:11Z</dc:date>
  </channel>
  <item rdf:about="http://hdl.handle.net/123456789/95">
    <title>Size-dependent enhancement of nonlinear optical properties in nanocolloids of ZnO</title>
    <link>http://hdl.handle.net/123456789/95</link>
    <description>Title: Size-dependent enhancement of nonlinear optical properties in nanocolloids of ZnO
Authors: litty irimpan, Bindu Krishnan; V.P.N. Nampoori, A Deepthi; P Radhakrishnan
Abstract: We have investigated the third-order nonlinearity in ZnO nanocolloids with particle sizes in the&#xD;
range 6–18 nm by the z-scan technique. The third-order optical susceptibility   3  increases with&#xD;
increasing particle size   R  within the range of our investigations. In the weak confinement regime,&#xD;
an R2 dependence of   3  is obtained for ZnO nanocolloids. The optical limiting response is also&#xD;
studied against particle size.</description>
    <dc:date>2008-02-11T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://hdl.handle.net/123456789/94">
    <title>Size dependent fluorescence spectroscopy of nanocolloids of ZnO</title>
    <link>http://hdl.handle.net/123456789/94</link>
    <description>Title: Size dependent fluorescence spectroscopy of nanocolloids of ZnO
Authors: litty irimpan, P. Radhakrishnan; V.P.N. Nampoori, A Deepthi; Bindhu Krishnan
Abstract: n this article we present size dependent spectroscopic observations of nanocolloids of ZnO. ZnO is&#xD;
reported to show two emission bands, an ultraviolet   UV   emission band and another in the green&#xD;
region. Apart from the known band gap 380 nm and impurity 530 nm emissions, we have found&#xD;
some peculiar features in the fluorescence spectra that are consistent with the nanoparticle size&#xD;
distribution. Results show that additional emissions at 420 and 490 nm are developed with particle&#xD;
size. The origin of the visible band emission is discussed. The mechanism of the luminescence&#xD;
suggests that UV luminescence of ZnO colloid is related to the transition from conduction band edge&#xD;
to valence band, and visible luminescence is caused by the transition from deep donor level to&#xD;
valence band due to oxygen vacancies and by the transition from conduction band to deep acceptor&#xD;
level due to impurities and defect states. A correlation analysis between the particle size and&#xD;
spectroscopic observations is also discussed.</description>
    <dc:date>2007-09-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://hdl.handle.net/123456789/93">
    <title>Nonlinear optical characteristics of self-assembled films of ZnO</title>
    <link>http://hdl.handle.net/123456789/93</link>
    <description>Title: Nonlinear optical characteristics of self-assembled films of ZnO
Authors: litty irimpan, A. Deepthy; Bindu Krishnan, V P N Nampoori; R Radhakrishnan
Abstract: In the present work, we have investigated the nonlinear optical properties of self-assembled films formed from&#xD;
ZnO colloidal spheres by z-scan technique. The sign of the nonlinear component of refractive index of the material remains&#xD;
the same; however, a switching from reverse saturable absorption to saturable absorption has been observed as the material&#xD;
changes from colloid to self-assembled film. These different&#xD;
nonlinear characteristics can be mainly attributed to ZnO defect states and electronic effects when the colloidal solution is&#xD;
transformed into self-assembled monolayers. We investigated&#xD;
the intensity, wavelength and size dependence of saturable and&#xD;
reverse saturable absorption of ZnO self-assembled films and&#xD;
colloids. Values of the imaginary part of third-order susceptibility are calculated for particles of size in the range 20–300 nm&#xD;
at different intensity levels ranging from 40 to 325 MW/cm2&#xD;
within the wavelength range of 450–650 nm.</description>
    <dc:date>2008-11-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://hdl.handle.net/123456789/92">
    <title>Excitation wavelength dependent fluorescence behaviour of nano colloids of ZnO</title>
    <link>http://hdl.handle.net/123456789/92</link>
    <description>Title: Excitation wavelength dependent fluorescence behaviour of nano colloids of ZnO
Authors: Litty Irimpan, Bindu Krishnan; A Deepthy, V P N Nampoori; P Radhakrishnan
Abstract: In this paper, the fluorescence behaviour of nano colloids of ZnO has been&#xD;
studied as a function of the excitation wavelength. We have found that&#xD;
excitation at the tail of the absorption band gives rise to an emission that&#xD;
shifts with the change of the excitation wavelength. The excitation&#xD;
wavelength dependent shift of the fluorescence maximum is measured to be&#xD;
between 60 and 100 nm. This kind of excitation wavelength dependent&#xD;
fluorescence behaviour, which may appear to be in violation of Kasha’s rule&#xD;
of excitation wavelength independence of the emission spectrum, has been&#xD;
observed for nano ZnO colloids prepared by two different chemical routes&#xD;
and different capping agents. It is shown that the existence of a distribution&#xD;
of energetically different molecules in the ground state coupled with a low&#xD;
rate of the excited state relaxation processes, namely, solvation and energy&#xD;
transfer, are responsible for the excitation wavelength dependent&#xD;
fluorescence behaviour of the systems.</description>
    <dc:date>2007-07-21T00:00:00Z</dc:date>
  </item>
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