Native defects in undoped and Ag-doped Hg0.78Cd0.22Te were studied usi
ng positron annihilation technique. For undoped specimens, the concent
ration of vacancy-type defects in subsurface regions (less than or equ
al to 500 nm) was higher than that in the bulk. This was attributed to
the introduction of Hg vacancies, V-Hg, resulting from the diffusion
of Hg atoms out of the specimen. Before Ag doping, the major species o
f vacancy-type defects in the specimens (p-type) nas identified as V-H
g, and the concentration of V-Hg was estimated to be 6 x 10(15) cm(-3)
After Ag doping, the concentration of vacancy-type defects was under
the detection limit of positron annihilation (less than or equal to 10
(14) cm(-3)). This was attributed to an occupation of Ag atoms at Hg s
ites, and the resultant decrease in the concentration of V-Hg. For the
Ag-doped specimens before and after thermal treatment, no large chang
e in the concentration of vacancy-type defects was observed. Thus, the
diffusion processes of Ag atoms are unlikely to involve the interacti
on between Ag atoms and V-Hg.