Results are presented of a study of Au/SiO2/a-Si: H MIS solar cells em
ploying wet-chemical oxides. The tunnel oxide can improve or deteriora
te the parameters of the solar cell, depending on the oxidation time a
nd on the percentage of the H2O2/water solution during the oxidation.
We use the difference in optical subgap absorption, determined by phot
othermal deflection spectroscopy and by the constant photocurrent meth
od, to follow the density of interface states N(ss) as a function of o
xidation time. In all cases, N(ss) goes through a maximum as a functio
n of time.