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CHEM01200604004 Shri Sanyasinaidu Boddu - Homi Bhabha ...

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3+ 3+<br />

Ce ions is in the ratio of around 40:60 for both SbPO 4 :Ce (2.5%), Tb 3+ (5%) nanoribbons/<br />

nanoparticles as well as the nanoribbons/ nanoparticles dispersed in silica, suggesting that the<br />

extent of energy transfer is approximately 60 %. The values are comparable with the energy<br />

transfer efficiency estimated from the Ce 3+ emission in SbPO 4 host using the equation η = 1-<br />

I/I0, where I and I 0 are the intensities of Ce emission in the presence and absence,<br />

respectively of Tb 3+ ions. The comparable efficiency of energy transfer for the as prepared<br />

nanomaterials and nanomaterials incorporated in silica matrix are understandable as the<br />

phonon energies are comparable for both SbPO and SiO<br />

4 2 lattices. Hence, identical extent of<br />

quenching is expected for lanthanide ion excited states from these matrices. However, the<br />

silica covering on the nanoribbons/ nanoparticles have additional advantage of removing the<br />

asymmetric environment created at the surface by the stabilising ligands. Energy transfer<br />

must also reflect in the Ce 3+ excited state lifetimes. However, the decay curves obtained<br />

corresponding to the excited state of Ce 3+ were close to the instrument response (less than 1<br />

ns) and hence the values could not be accurately calculated from the decay curves.<br />

3+<br />

It will be interesting to understand the mechanism of the energy transfer between the<br />

3+ 3+ 3+ 3+<br />

Ce and Tb ions. The energy transfer between Ce and Tb depends on extent of overlap<br />

between donor (D) emission peak (Ce 3+ emission peak in the present case) and acceptor (A)<br />

absorption peak (Tb 3+ excitation peak in the present case) and expressed by the equation 21<br />

[69],<br />

4 π | , *| | *, |<br />

2<br />

DA DA D ( ).<br />

A (<br />

P = < D A H D A> g E g E)<br />

h<br />

∫ dE……………….. (21)<br />

where, P DA is the rate of energy transfer from donor to acceptor. The first term in the above<br />

expression represents the transition dipole moment between the |D*, A> and |D, A*> states<br />

via the interaction Hamiltonian H DA . D* and A* represent the excited state of the donor and<br />

acceptor, H is the interaction Hamiltonian. The parameters g<br />

DA<br />

D(E) and g A (E) are normalized<br />

population density function representing the optical line shapes of donor and acceptor<br />

132

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