Coupled radiotracer and voltammetric study of the adsorption of 1-hydroxy-ethane-1,1-diphosphonic acid on polycrystalline gold

Coupled application of a version of the in-situ radiotracer 'foil' method and voltammetry provided information on the time-, potential-, concentration- and pH-dependent adsorption of l-hydroxy-ethane-l, l-diphosphonic acid (HEDP) on a polycrystalline gold electrode, and on the effect of Zn2+ ions on the adsorption phenomena. Adsorption processes on the oxide-free surface of gold were observed to be potential-dependent in the potential range 0.05-1.00 V (versus RHE), while formation and irreversible accumulation of oxidation products of HEDP could be detected at E > 1.00 V. The relative adsorption strength of HEDP (its dissociation and/or oxidation products) was found to be higher on an oxide-free gold surface than on an oxide-covered one. The surface excess of HEDP increased with increasing pH. Addition of Zn2+ ions to the solution exerted a substantial effect on the HEDP accumulation. Namely, significant differences in the surface coverage, as well as in the kinetics and mechanism of HEDP adsorption could be detected in the potential regions below and above E = 0.2 V. Reduction of Zn(II) species at E less than or equal to 0.1 V is probably coupled with the induced adsorption of HEDP on an Au electrode, leading to the formation of a polymolecular HEDP-Zn surface complex layer. (C) 2000 Elsevier Science S.A. All rights reserved.