Visible emissions at 548, 528 and 660 nm have been observed from the sol-ge
l derived nanocrystalline Er3+:BaTiO3 powders under infrared excitations at
both 980 and 810 nm. Combined with the energy level structure of Er3+ and
the decay kinetics of the green emissions, the up-conversion mechanism has
been analyzed and explained. The bright green emission at 548 nm has been a
ttributed to the ground state-directed transition from S-4(3/2), which is p
opulated through excited state absorption (ESA) for 810 nm excitation, and
through both ESA and energy transfer (ET) processes for 980 nm excitation.
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