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CHEM01200604004 Shri Sanyasinaidu Boddu - Homi Bhabha ...

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nanocrystals is shown in Fig.10 [58]. The spectrum is characterised by mainly two peaks, one<br />

sharp peak around 382 nm and other broad peak around 500 nm. The sharp peak has been<br />

attributed to the band edge emission and the broad peak to the recombination of electrons<br />

trapped at the oxygen defect levels and holes in the valance band of ZnO. It is observed that<br />

the emission maximum is shifted in the visible regions depending on the synthesis conditions<br />

and annealing temperatures [57].<br />

Normalised Intensity<br />

1.0<br />

0.8<br />

0.6<br />

0.4<br />

0.2<br />

0.0<br />

Band edge<br />

emission<br />

λ exc<br />

= 325 nm<br />

Defect emission<br />

400 450 500 550 600<br />

wavelength (nm)<br />

Fig.10. Representative emission spectrum from ZnO nanocrystals obtained after excitation at<br />

325 nm [58].<br />

BaSnO 3 belongs to the family of cubic perovskite structure and exhibit interesting<br />

optical and electrical properties. Mizoguchi, et al. [59] observed emission around 590 nm<br />

from BaSnO 3 powder samples at low temperatures with corresponding excited state lifetime<br />

of ~ 10μs. These authors have also observed emission in the near-infrared region form these<br />

samples. SnO 2 is a direct band gap n-type semiconductor (E g = 3.6 eV). It is extensively used<br />

for making sensors and optical devices [60-62]. Many authors have reported synthesis of<br />

luminescent SnO 2 nanoparticles. For example, Gu, et al. [63] have reported the preparation of<br />

SnO 2 nanoparticles by sol-gel method using SnCl 4·5H 2 O and NH 4 OH followed by heating<br />

over the temperature range of 400 - 600°C. These particles showed luminescence around 400<br />

nm characteristic of oxygen vacancies present in the nanoparticles and its intensity decreased<br />

on increasing heat treatment temperature.<br />

23

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