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CHEM01200604004 Shri Sanyasinaidu Boddu - Homi Bhabha ...

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in the ZnGa 2 O 4 lattice. It is known that In 3+ is heavier than Ga 3+ , as a result the energy<br />

corresponding to GaO 6 unit in the ZnGa 2-x In x O 4 nanoparticles will be less than that in<br />

ZnGa 2 O 4 . Hence, the λ max corresponding to emission and excitation of GaO 6 level shifts to<br />

higher values with increase in the In 3+ content. The decay curve corresponding to the excited<br />

state of blue emission from ZnGa 1.5 In 0.5 O 4 nanoparticles is shown in Fig.100 (b). It is found<br />

to be bi-exponential in nature with lifetime values 0.49 μs (56 %) and 1.85 μs (44 %). The<br />

faster component is due to surface GaO 6 units and longer component is due to GaO 6 present<br />

in the bulk of the ZnGa 2 O 4 :In 3+ lattice. Since surface GaO 6 units are directly bound to EG<br />

moiety, they will decay faster than bulk GaO 6 structural units.<br />

(a)<br />

(b)<br />

Fig.99. (a) TEM image, (b) HRTEM image of ZnGa 1.5 In 0.5 O 4 nanoparticles. SAED pattern<br />

from these nanoparticles is shown in the inset of Fig.99 (a)<br />

Normalised intensity<br />

1.0<br />

0.8<br />

0.6<br />

0.4<br />

0.2<br />

x = 0<br />

x = 0.05<br />

x = 0.2<br />

x = 0.5<br />

Intensity (arb.units)<br />

1000<br />

100<br />

λ exc<br />

= 270 nm & λ em<br />

= 455 nm<br />

0.0<br />

10<br />

350 400 450 500 550 600 0 5 10 15 20<br />

Wavelength (nm)<br />

Time (μs)<br />

(a)<br />

(b)<br />

Fig.100. (a) Emission spectra of ZnGa 2-x In x O 4 (x = 0, 0.05, 0.2, 0.5) nanoparticles after<br />

exciting samples in the UV region (260 to 280 nm). (b) Decay profile corresponding<br />

to blue emission from ZnGa 1.5 In 0.5 O 4 nanoparticles.<br />

160

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