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Engineered ZnO/Ti3C2Tx MXene heterostructures with optimized composition for dual-function photocatalytic degradation and pathogenic inactivation

  • Taghreed Al-Mutairi
  • , Ridha Hamdi*
  • , Tahani Al-ghamidi
  • , Muhammad Younas
  • , Hafedh Kochkar*
  • , Amor Ben Ali
  • , Essam Kotb
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

In this study, we report the synthesis of Ti3C2Tx MXene/ZnO heterojunction derived from Ti3AlC2 MAX phase precursor. High-resolution transmission electron microscopy (HRTEM) and selected area electron diffraction (SAED) reveal attachment of ZnO nanoparticles onto the MXene basal plane, characterized by distinct interfacial lattice aberrations and the retention of the hexagonal Ti-C framework along the [0001] zone axis. X-ray photoelectron spectroscopy (XPS) confirms the formation of covalent Ti-O-Zn bridging bonds, which act as a chemical “glue” to facilitate electronic communication. Electrochemical impedance spectroscopy (EIS) demonstrates a dramatic reduction in charge-transfer resistance (from 131 MΩ to 5 kΩ) and a fast relaxation time of about 7 µs. The ZM5 composite exhibits superior multi-functional performance, achieving a 58.7% degradation efficiency of formic acid and potent antibacterial activity with inhibition zones up to 16 mm against S. Enteritidis. These results pave the way for the design of chemically anchored 2D heterojunctions optimized for advanced environmental remediation and antimicrobial technologies.

Original languageEnglish
Article number114307
JournalMaterials Research Bulletin
Volume204
DOIs
StatePublished - Nov 2026

Bibliographical note

Publisher Copyright:
© 2026 Elsevier Ltd

Keywords

  • 2D heterostructures
  • Antibacterial activity
  • Interfacial charge transfer
  • MXenes
  • Photocatalysis
  • Ti-O-Zn covalent bonding
  • ZnO nanoparticles

ASJC Scopus subject areas

  • General Materials Science
  • Condensed Matter Physics
  • Mechanics of Materials
  • Mechanical Engineering

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