The kinetics of forward and backward energy transfer processes in fluoroind
ate glasses double doped with Yb3+ and Er3+ has been studied. It was possib
le to excite selectively Yb3+ ions and detect emission due only to these io
ns or combined with the emission coming from the Er3+ ions. At low concentr
ation of Yb3+ (0.1 mol %) the emission decay of these ions is nonexponentia
l when there is back transfer from Er3+ ions; the dynamics is well describe
d using the fluorescence "transfer function" model. Moreover, the evolution
of the emission from the I-4(11/2) (Er3+) level is in good agreement with
the behavior predicted by the model. The critical radii obtained from the f
itting for forward and backward energy transfer are compared with those cal
culated with the Dexter formula. When the Yb3+ concentration is increased,
the migration among these ions is very important and the emission decay of
the Yb3+ ions is nearly exponential with the lifetime of these ions. This b
ehavior is explained considering that, at high Yb3+ concentration and due t
o the migration, the transfer from Yb3+ to Er3+ ions is restricted to very
closed couples of ions with high back transfer probability. The limitations
of the fluorescence "transfer function" model associated with the correlat
ion effect in the excitation of Er3+ ions by energy transfer are discussed.
(C) 1999 American Institute of Physics. [S0021-8979(99)00814-2].