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  <title>DSpace Collection:</title>
  <link rel="alternate" href="http://pucir.inflibnet.ac.in:8080/jspui/handle/123456789/610" />
  <subtitle />
  <id>http://pucir.inflibnet.ac.in:8080/jspui/handle/123456789/610</id>
  <updated>2026-04-30T23:17:52Z</updated>
  <dc:date>2026-04-30T23:17:52Z</dc:date>
  <entry>
    <title>Luminescence properties of Ln3+ doped BaMoO4 (Ln3+ = Sm3+ and Dy3+) phosphors under UV excitation</title>
    <link rel="alternate" href="http://pucir.inflibnet.ac.in:8080/jspui/handle/123456789/615" />
    <author>
      <name>Devi Victory, CH</name>
    </author>
    <id>http://pucir.inflibnet.ac.in:8080/jspui/handle/123456789/615</id>
    <updated>2024-06-12T09:49:50Z</updated>
    <published>2023-01-01T00:00:00Z</published>
    <summary type="text">Title: Luminescence properties of Ln3+ doped BaMoO4 (Ln3+ = Sm3+ and Dy3+) phosphors under UV excitation
Authors: Devi Victory, CH
Abstract: Ln3+ doped BaMoO4 (Ln 3+ = Sm3+ and Dy3+) nanoparticles have been synthesized successfully using ethylene&#xD;
glycol as a solvent. All the prepared samples are well indexed into the pure scheelite-type tetragonal structure of&#xD;
BaMoO4, the doping of trivalent ions (Ln3+) in to the bivalent host ions (Ba2+) sites of the BaMoO4 do not change&#xD;
the pure tetragonal structure of BaMoO4 although there is a charge difference between Ba2+ and Ln3+. The SEM&#xD;
image of the prepared BaMoO4 samples shows a number of uniform shuttle-like nanocrystalline with protrusion&#xD;
in the middle. The doping of Ln3+ ions do not change the morphology of the BaMoO4. The photoluminescence&#xD;
study has been carried in detail by measuring the excitation and emission spectra of the prepared samples. The&#xD;
excitation spectrum consists of a broad band with a maximum at about 268 nm thereby demonstrating the&#xD;
transfer of energy from MoO24 - groups to the doped Ln3+ ions. Yellow emission is dominated over blue in case of&#xD;
Dy3+ doped BaMoO4 and in Sm3+ doped BaMoO4 red emission dominated over other lights under UV excitation.&#xD;
The luminescence intensity is highest at 10 at.% Ln3+ under the UV excitation. Under this UV excitation BaMoO4:&#xD;
Sm3+ exhibits strong orange-red and BaMoO4:Dy3+ greenish-yellow emissions. Excitation of Dy3+ in thin film of&#xD;
BaMoO4 emits an intense yellow color which could be applicable in the field of biological assays and biological&#xD;
fluorescence labeling.</summary>
    <dc:date>2023-01-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Effect of annealing on the luminescence properties of YVO4:Dy3+ phosphor on co-doping Pb2+ ions</title>
    <link rel="alternate" href="http://pucir.inflibnet.ac.in:8080/jspui/handle/123456789/614" />
    <author>
      <name>Devi Victory, CH</name>
    </author>
    <id>http://pucir.inflibnet.ac.in:8080/jspui/handle/123456789/614</id>
    <updated>2024-06-12T09:45:16Z</updated>
    <published>2015-03-09T00:00:00Z</published>
    <summary type="text">Title: Effect of annealing on the luminescence properties of YVO4:Dy3+ phosphor on co-doping Pb2+ ions
Authors: Devi Victory, CH
Abstract: Pb2+ co-doped YVO4:Dy3+ phosphors have been synthesized at a relatively low temperature of 120  C via&#xD;
ethylene glycol route. The samples are further annealed at 500 and 900  C. The prepared samples were&#xD;
characterized by XRD, SEM, spectra energy dispersive analysis of X-ray (EDAX) and photoluminescence&#xD;
spectroscopy. XRD patterns of all samples are well indexed with single tetragonal phase of YVO4. The&#xD;
emission intensity of Dy3+ is significantly enhanced on co-doping Pb2+ ions. The highest emission is&#xD;
obtained at 7 at.% Pb2+ for 900  C annealed samples. Both emission intensity and decay lifetime increases&#xD;
on annealing the samples from 500 to 900  C. On co-doping Pb2+ into YVO4:Dy3+ phosphors, the emission&#xD;
color falls near the white region and then shift towards yellow region on annealing from 500 to 900  C&#xD;
thereby indicating that annealing temperature play a role on tuning the color of the phosphors. As well&#xD;
as the emission color of the phosphors remain the same even on changing the excitation wavelengths&#xD;
from 280 nm, which would serve as potential phosphors for white emission in LED applications.</summary>
    <dc:date>2015-03-09T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Comparative absorption spectroscopy involving 4f–4f transitions to explore the kinetics of simultaneous coordination of uracil with Nd(III) and Zn(II) and its associated thermodynamics</title>
    <link rel="alternate" href="http://pucir.inflibnet.ac.in:8080/jspui/handle/123456789/613" />
    <author>
      <name>Devi Victory, CH</name>
    </author>
    <id>http://pucir.inflibnet.ac.in:8080/jspui/handle/123456789/613</id>
    <updated>2024-06-12T09:42:44Z</updated>
    <published>2011-06-13T00:00:00Z</published>
    <summary type="text">Title: Comparative absorption spectroscopy involving 4f–4f transitions to explore the kinetics of simultaneous coordination of uracil with Nd(III) and Zn(II) and its associated thermodynamics
Authors: Devi Victory, CH
Abstract: The interaction of uracil with Nd(III) has been explored in presence and absence of Zn(II) using the comparative&#xD;
absorption spectroscopy involving the 4f–4f transitions in different solvents. The complexation&#xD;
of uracil with Nd(III) is indicated by the change in intensity of 4f–4f bands expressing in terms of significant&#xD;
change in oscillator strength and Judd–Ofelt parameters. Intensification of this bands became&#xD;
more prominent in presence of Zn(II) suggesting the stimulative effect of Zn(II) towards the complexation&#xD;
of Nd(III) with uracil. Other spectral parameters namely Slator–Condon (Fk’s), nephelauxetic effect&#xD;
(ˇ), bonding (b1/2) and percent covalency (ı) parameters are computed to correlate their simultaneous&#xD;
binding of metal ions with uracil. The sensitivities of the observed 4f–4f transitions towards the&#xD;
minor coordination changes around Nd(III) has been used to monitor the simultaneous coordination of&#xD;
uracil with Nd(III) and Zn(II). The variation of intensities (oscillator strengths and Judd–Ofelt parameters)&#xD;
of 4f–4f bands during the complexation has helped in following the heterobimetallic complexation&#xD;
of uracil. Rate of complexation with respect to hypersensitive transition was evaluated. Energy&#xD;
of activation and thermodynamic parameters for the complexation reaction were also determined.</summary>
    <dc:date>2011-06-13T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Absorption spectroscopic probe to investigate the interaction between Nd(III) and calf-thymus DNA</title>
    <link rel="alternate" href="http://pucir.inflibnet.ac.in:8080/jspui/handle/123456789/612" />
    <author>
      <name>Devi Victory, CH</name>
    </author>
    <id>http://pucir.inflibnet.ac.in:8080/jspui/handle/123456789/612</id>
    <updated>2024-06-12T09:40:02Z</updated>
    <published>2010-12-25T00:00:00Z</published>
    <summary type="text">Title: Absorption spectroscopic probe to investigate the interaction between Nd(III) and calf-thymus DNA
Authors: Devi Victory, CH
Abstract: The interaction between Nd(III) and Calf Thymus DNA (CT-DNA) in physiological buffer (pH 7.4) has been&#xD;
studied using absorption spectroscopy involving 4f–4f transition spectra in different aquated organic&#xD;
solvents. Complexation with CT-DNA is indicated by the changes in absorption intensity following the&#xD;
subsequent changes in the oscillator strengths of different 4f–4f bands and Judd–Ofelt intensity (T )&#xD;
parameters. The other spectral parameters namely Slator–Condon (Fk’s), nephelauxetic effect (ˇ), bonding&#xD;
(b1/2) and percent covalency (ı) parameters are computed to correlate with the binding of Nd(III) with&#xD;
DNA. The absorption spectra of Nd(III) exhibited hyperchromism and red shift in the presence of DNA.&#xD;
The binding constant, Kb has been determined by absorption measurement. The relative viscosity of DNA&#xD;
decreased with the addition of Nd(III). Thermodynamic parameters have been calculated according to&#xD;
relevant absorption data and Van’t Hoff equation. The characterisation of bonding mode has been studied&#xD;
in detail. The results suggested that the major interaction mode between Nd(III) and DNA was external&#xD;
electrostatic binding.</summary>
    <dc:date>2010-12-25T00:00:00Z</dc:date>
  </entry>
</feed>

