Affiliations 

  • 1 Department of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Negeri Jakarta, Jl. Rawamangun Muka, Jakarta Timur 13220, Indonesia
  • 2 School of Materials Science, Japan Advanced Institute of Science and Technology, 1-1 Asahidai, Nomi, Ishikawa 923-1292, Japan
  • 3 The Centre for Science Innovation, Jakarta 13120, Indonesia
  • 4 Department of Physics, Faculty of Mathematics and Natural Sciences, Universitas Indonesia, Depok 16424, Indonesia
  • 5 Institute of Microengineering dan Nanoelectronics, Universiti Kebangsaan Malaysia, Selangor 43600, Malaysia
R Soc Open Sci, 2023 Jun;10(6):230247.
PMID: 37351492 DOI: 10.1098/rsos.230247

Abstract

A pure-phase Cu2O film photocatalyst was successfully prepared by the electrodeposition technique from a non-pH-adjusted solution. To investigate the phase evolution and photocatalytic activity of the film, the electrodeposition was conducted at different deposition temperatures. Photocatalytic activity of the films was evaluated from methylene blue (MB) dye degradation. The Cu2O phase initially appeared at room temperature and its fraction was found to increase with increasing the deposition temperature, while the impurity phase was successfully diminished. A pure Cu2O film with a narrow optical bandgap energy of 1.96 eV was obtained at 75°C. The multi-faceted crystals were found to form at 45°C and became a truncated octahedral structure that possessed {111} and {100} facets as deposition temperature further increased. A preferred orientation growth of {110} facet, which is known to possess a relatively high surface energy, was produced at 75°C. The performance of MB photodegradation enhanced gradually by increasing the deposition temperature. The increase of photocatalytic activity could be attributed to the rise of photoelectrochemical response and the decrease of resistance charge transfer because of narrowing bandgap energy, increasing Cu2O fraction, and growing a relatively high catalytic activity facet which had escalated redox reaction that decomposed MB at the photocatalyst-solution interface.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.