3.8 Proceedings Paper

Nucleation and growth mechanism of cuprous oxide electrodeposited on ITO substrate

Journal

MATERIALS TODAY-PROCEEDINGS
Volume 66, Issue -, Pages 187-195

Publisher

ELSEVIER
DOI: 10.1016/j.matpr.2022.04.445

Keywords

Cyclic voltammetry; Chronoamperometry; Nucleation; Growth; Cuprous oxide; Electrodeposition; Band gap

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The electrodeposition mechanisms of Cu2O on ITO were investigated using cyclic voltammetry and chronoamperometry methods. The results showed that Cu2O electrodeposition occurs through cathodic reduction and is a quasi-reversible reaction controlled by the diffusion of copper ions. The deposition mechanism on ITO substrate follows an instantaneous three-dimensional nucleation controlled by diffusion.
The electrodeposition mechanisms of cuprous oxide (Cu2O) from copper nitrate solutions on indium tin oxide (ITO) were investigated using the cyclic voltammetry and the chronoamperometry methods. Then the kinetics parameters, nucleation and growth mechanism were explored. The CV measurement showed that the electrodeposition of Cu2O takes place by cathodic reduction at potential -0.5 V versus saturated calomel electrode (SCE). Furthermore, the voltammograms at different scan rates revealed that the electrodeposition reaction of Cu2O is a quasi-reversible reaction controlled by the diffusion of copper ions. Moreover, the deposition mechanism of Cu2O on the ITO substrate determined by the Astley approach and confirmed by the Scharifker-Hills models follows an instantaneous three-dimensional (3D) nucleation controlled by diffusion with an average diffusion coefficient D of 0.549 10-6 cm2 s-1. The X-ray diffraction pattern of Cu2O film was indexed to cubic crystal structure. The scanning electron microscopy analysis indicated that the average size of the cuprous oxide particles is about 1.408 lm. The optical energy band gap (Eg) was calculated by Tauc's plot for Cu2O is 2.16 eV. The theoretical analyses reveal that Cu2O has an energy band gap of 2.25 eV, which corresponds to experimental results. Copyright (c) 2022 Elsevier Ltd. All rights reserved. Selection and peer-review under responsibility of the scientific committee of the 4thInternational Conference on Advanced Materials for Photonics, Sensing and Energy Conversion Energy Applications.

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