Electrodeposition of bismuth onto glassy carbon electrodes from nitrate solutions

Abstract

The electrodeposition of bismuth on glassy carbon electrodes (GCEs) from nitrate solutions was studied by cyclic voltammetry, chronoamperometry, and scanning electron microscopy. Cyclic voltammograms exhibit a crossover between the cathodic and anodic branches, characteristic of the formation of bismuth nuclei on GCEs. The bismuth electrodeposition on GCEs is a diffusion-controlled reaction. The current transients for bismuth electrodeposition were analyzed according to the Scharifker–Hills models, the Scharifker’s general equation and the Heerman–Tarallo equation. For 1 and 5 mM Bi 3+, the nucleation and growth mechanism is independent of deposition potential and follows the three-dimensional (3D) progressive nucleation and growth model. However, a deposition potential dependence of nucleation and growth mechanism can be found in the cases of 10 and 20 mM Bi 3+. The quantitative analysis by the two equations shows that A and N 0 exponentially grow with the increase of deposition potential, while D decays in an exponential mode. It should be noted that the two equations produced the very close N 0 and D values and the distinct A values (especially at −300 and −350 mV). However, the critical size of the nuclei ( N c) estimated by using the two equations was all zero. Both of the equations can be used for describing the electrodeposition of bismuth on GCEs in this work. SEM images show that high deposition potential as well as high concentration can enhance the nuclei density of bismuth on GCEs and favors the formation of small crystallites with a less defined structure.