We have investigated the optical properties of Se clusters/particles incorp
orated into porous glasses as well as into zeolites in order to explore the
effect of geometrical constraints on the electronic states of Se. It has b
een found that the optical gap E-0, of Se shifts to higher energy in porous
glasses, depending on the pore diameter D; Delta E-0 proportional to D-0.5
. The observation indicates that carriers in extended (nonlocalized) states
of amorphous Se are not simply confined in zero dimension as the pore size
decreases, but are confined and/or localized in the unique geometrical por
e structure. On the other hand, the electronic slates of Se clusters in zeo
lites are modulated by the absence of inter-molecular (ring or chain) inter
action, and are influenced by the interaction between lone pair electrons o
f Se and cations of the framework of zeolites.