We examine various properties of photoluminescence due to the Mn2+ 3d intra
-shell transition and the transition involving the trap state in Mn2+ doped
CdS nanocrystals. It is shown that the dominant excitation mechanism of th
e Mn2+ ions under the interband excitation is the energy transfer from the
electron-hole pairs delocalized inside the nanocrystals while the contribut
ion of the energy transfer from the trap state to the excitation of Mn2+ is
negligibly small. It is proved that the interaction of the 3d electrons of
Mn2+ with the photo-generated electron-hole pairs is insignificant compare
d with the crystal-field interaction acting on these electrons, contrary to
the strong sp-d wavefunction mixing model proposed previously. In addition
, it is found that the peak position of the Mn2+ luminescence spectrum is s
hifted significantly to higher energies on increasing the interband excitat
ion photon energy, indicating that the luminescence spectrum of Mn2+ is dep
endent on the crystallite size. A probable cause of this result is shown to
be the surface effect on the phonon density of states. (C) 2001 Elsevier S
cience Ltd. All rights reserved.