Anodic treatment of p-Cd1-xZnxTe (x = 0, 0.05, and 0.12) in 0.5 M H2SO4 lea
ds to the formation of a network of pores which can extend more than 100 mu
m below the top surface. Photocurrent spectroscopy reveals the presence of
Te-o on the surface of the pores. The Te-o film is on average thin (less t
han or equal to 5 Angstrom), in contrast to the thicker film obtained by ph
otoanodic etching of n-CdTe. The photocurrent spectra are affected not only
by the absorbance of Te-degrees, but also by recombination in the porous l
ayer. (C) 2000 The Electrochemical Society. S0013-4651(00)02-066-8. All rig
hts reserved.