The interactions of iodide ions with cuprite (Cu2O) surfaces were studied b
y combining batch experiments and surface analyses. The evolution of iodide
uptake with pH was investigated. The thermodynamical calculations and surf
ace analyses (X-ray photoelectron spectroscopy, scanning electron microscop
y, Raman spectroscopy, and electrochemistry) were used to show that two dif
ferent pH-dependent mechanisms are responsible fbr the accumulation of the
iodide species on Cu2O. At pH values lower than 6.5, the precipitation of C
uI occurs on the cuprite surface, while in more alkaline medium, the iodide
adsorption takes place by substituting the surface hydroxyl groups of Cu2O
. The sorption processes were not affected by a 1000-fold excess of chlorid
e ions, but they were limited to the potential range corresponding to the s
tability domain of Cu2O (i.e., between -10 and +190 mV/ENH at pH 8); thus n
o accumulation was observed either on metallic copper or on CuO.