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Enriched photocatalytic and photoelectrochemical activities of a 2D/0D g-C3N4/CeO2 nanostructure

  • Ramaraghavulu Rajavaram
  • , S. V. Prabhakar Vattikuti*
  • , Jaesool Shim*
  • , Xinghui Liu
  • , Nguyen To Hoai*
  • , Nam Nguyen Dang
  • *Corresponding author for this work

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

32 Downloads (CityUHK Scholars)

Abstract

Sunlight-powered photocatalysts made from CeO2 nanosized particles and g-C3N4 nanostructures were produced through a thermal decomposition process with urea and cerium nitrate hexahydrate. The preparation of g-C3N4, CeO2, and a binary nanostructured g-C3N4/CeO2 photocatalyst was done through a facile thermal decomposition method. The structural properties were analyzed using powder X-ray diffraction, scanning electron microscopy, high-resolution transmission electron microscopy, energy dispersive X-ray spectroscopy, and X-ray photoelectron spectroscopy (XPS). Photocatalyst properties were characterized by using crystal violet (CV), a UV-Vis spectrophotometer, photocurrent and electron impedance spectroscopy (EIS). The structural and morphological analyses revealed that the g-C3N4/CeO2 nanostructures significantly enhanced the photoactivity for CV dye degradation under simulated sunlight, with a degradation rate of 94.5% after 105 min, compared to 82.5% for pure g-C3N4 and 45% for pure CeO2. This improvement was attributed to the noticeable visible light absorption and remarkable charge separation abilities of the nanostructures. Additionally, the g-C3N4/CeO2 nanostructures showed notable PEC performance under simulated sunlight. This study presents an easy and efficient method for producing g-C3N4 photocatalysts decorated with semiconductor materials and provides insights for designing nanostructures for photocatalytic and energy applications. © 2023 The Author(s). Published by the Royal Society of Chemistry.
Original languageEnglish
Pages (from-to)6489–6500
JournalNanoscale Advances
Volume5
Issue number23
Online published9 Oct 2023
DOIs
Publication statusPublished - 7 Dec 2023

Publisher's Copyright Statement

  • This full text is made available under CC-BY-NC 3.0. https://creativecommons.org/licenses/by-nc/3.0/

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