Voltammetric and chronoamperometric studies of silver electrodeposition from a bath containing HEDTA

The electrodeposition of silver on platinum from ammonium-buffered solutions containing HEDTA (N-(2-hydroxyethyl)ethylenediaminetriacetic acid) at various concentrations was investigated. Potentiometric titration and voltammetric studies indicated that in the presence of 2.0 · 10–1 M HEDTA, the deposited silver was reduced from a mixture of [AgHEDTA]2– and [Ag(NH3)2]+ complexes, whereas at 2.0 · 10–2 M and 2.0 · 10–3 M HEDTA in the electrolyte, the silver was reduced from the [Ag(NH3)2]+ complexes alone. Hydrodynamic studies showed variation in the diffusion coefficient for the electroactive species in solution, depending on the HEDTA concentration. Chronoamperometric study in a solution containing 2.0 · 10–1 M HEDTA at low overpotential (0.000 V to –0.050 V) showed a transition from progressive to instantaneous nucleation in a single current transient, whereas, at –0.200 V only 3Dprogressive nucleation controlled by mass transport was observed. Scanning electron microscope images showed that the silver films produced in silver baths with HEDTA were uniform, without cracks, and fine-grained, regardless of its concentration, while in the absence of HEDTA the morphology was rough and dendritic. X-ray diffraction analysis of the films obtained at various HEDTA concentrations revealed polycrystalline silver, similar to film obtained in cyanide and EDTA/ammonia baths.