Related Experiment Video
Updated: Aug 6, 2026

Photochemical Oxidative Growth of Iridium Oxide Nanoparticles on CdSe@CdS Nanorods
Published on: February 11, 2016
g-C3N4 Modified with Metal Sulfides for Visible-Light-Driven Photocatalytic Degradation of Organic Pollutants
Shoaib Mukhtar1, Erzsébet Szabó-Bárdos1, Csilla Őze2
1Research Group of Environmental and Inorganic Photochemistry, Center for Natural Sciences, Faculty of Engineering, University of Pannonia, P.O. Box 158, H-8201 Veszprém, Hungary.
Abstract:
Graphitic carbon nitride (g-C3N4) proved to be a promising semiconductor for the photocatalytic degradation of various organic pollutants. However, its efficacy is limited by a fast electron hole recombination, a restricted quantity of active sites, and a modest absorption in the visible range. To overcome these limitations, g-C3N4-Bi2S3 and g-C3N4-ZnS composites were effectively produced utilizing a starch-assisted technique. The findings from FT-IR, XRD, EDX, XPS, BET, SEM, and TEM demonstrated that the enhanced photocatalytic activity of g-C3N4-Bi2S3 and g-C3N4-ZnS composites was primarily due to their improved photocarrier separation and transfer rates. The photocatalyst facilitated the aerobic photocatalytic degradation of colorless contaminants such as coumarin and para-nitrophenol (4-NP). For the decomposition of 4-NP, g-C3N4-Bi2S3 exhibited a maximum efficiency of 90.86% in UV light and 16.78% in visible light, with rate constants of 0.29 h-1 and 0.016 h-1, respectively. In contrast, g-C3N4-ZnS demonstrated a maximum efficiency of 100% in UV light and 15.1% in visible light, with rate constants of 0.57 h-1 and 0.018 h-1, respectively. The bioinspired synthesis combined with the modification with metal sulfides proved to considerably enhance the photocatalytic activity of g-C3N4, increasing its potential for practical applicability in environmentally friendly water treatment systems for the efficient removal of recalcitrant organic contaminants.
![Cercosporin-Photocatalyzed [4+1]- and [4+2]-Annulations of Azoalkenes Under Mild Conditions](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F60786.jpg&w=3840&q=50)
