Facile Synthesis of g-C3N4/MnO2Composites with Dual Functional Activity of Photodegradation of Pollutants and Antimicrobial Efficacy

  • Paramasivam Shanmugam
  • , Mani Arivazhagan
  • , Alvin Lim Teik Zheng
  • , Lalitha Gnanasekaran
  • , Hongyi Gao
  • , Joon Ching Juan
  • , Pariya Na Nakorn
  • , Supakorn Boonyuen

Producción científica: Contribución a una revistaArtículorevisión exhaustiva

Resumen

Increasing environmental contamination and spread of drug-resistant microbials leading to water pollution and antimicrobial resistance is a critical issue worldwide. This study describes the synthesis of multifunctional heterojunction g-C3N4/MnO2 composite as a potential photocatalyst for environmental remediation and microbial inactivation under visible light. Initially, graphitic carbon nitride (g-C3N4) was prepared by a thermal polycondensation method. Further, the multifunctional heterojunction g-C3N4/MnO2 composite with uniform MnO2 nanoparticle (NP) distribution is developed via a simple hydrothermal process. The g-C3N4/MnO2 composites were examined through the degradation of tetracycline (TC) and methylene blue (MB). As a result, the composite materials demonstrated superior photocatalytic efficiency than MnO2 and g-C3N4, due to the composite materials’ enhanced charge separation and extended to the visible light region. Remarkably, degradation efficiencies of 95.38% for MB and 91.97% for TC were achieved within 180 min. Further, antibacterial activity was tested against Escherichia coli and Staphylococcus aureus using the agar–agar well diffusion method. The obtained zone inhibition values reveal that as-prepared g-C3N4/MnO2 composites have strong antimicrobial properties. These results demonstrate that g-C3N4/MnO2 composites are cost-effective, sustainable, and multifunctional materials with promising applications in wastewater treatment through simultaneous degradation of organic pollutants and microbial inactivation.

Idioma originalInglés
Páginas (desde-hasta)9117-9128
Número de páginas12
PublicaciónACS Omega
Volumen11
N.º6
DOI
EstadoPublicada - 17 feb. 2026

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