Upon potential cycling in acidic electrolyte, the coverage of Ge electrodes
call be changed from GeH to GeOH. In situ infrared spectroscopy reveals th
at hydrogen adsorbs and desorbs at Ge in mono- and dihydride configurations
. Comparison of (111)- and (100)-oriented electrodes shows that the Ge surf
ace is rough at the atomic scale and that this roughening takes place throu
gh(lll) microfacetting. This facetting call account for the attenuated pola
rization dependence of the GeH absorption and its enhancement through local
field effects. Finally, the band edge shifts which are observed upon hydro
gen adsorption/desorption appear related to a change in the Ge surface char
ge rather than to a dipolar effect. (C) 1999 Elsevier Science B.V. All righ
ts reserved.