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In situ synthesis of MXene@Iron oxide nanoparticle composites via pulsed laser ablation in liquid applied for electrochemical H2O2 reduction

  • Lenka Lorencová
  • , Eva Noskovičová
  • , Monika Jerigová
  • , Monika Stupavská
  • , Ľubomír Orovčík
  • , Lucia Kopčanová
  • , Peter Kasák
  • , Andrej Vikartovský
  • , Dušan Lorenc
  • , Khaled A. Mahmoud
  • , J. Tkáč*
  • *Corresponding author for this work
  • Slovak Academy of Sciences
  • Comenius University
  • International Laser Centre Bratislava
  • Masaryk University
  • Center for Advanced Materials

Research output: Contribution to journalArticlepeer-review

Abstract

We propose to circumvent the lack of intrinsic magnetism in MXenes by in situ decorating the samples with magnetic nanoparticles during laser ablation in liquid by deposition of iron species on three types of MXenes (nanocomposites). The basic properties of such nanocomposites were characterized by a number of techniques including Scanning Electron Microscopy (SEM), Secondary Ion Mass Spectrometry (SIMS), X-ray Photoelectron Spectroscopy (XPS), electrochemical investigation and the optical Faraday effect. The results indicate significant differences in the content of Fe species deposited on MXenes (Ti3C2Tx; Nb2CTx and Nb4C3Tx) and the amount of Fe species deposited on MXenes is triggered by the density of plasmons present within MXenes. Moreover, we confimed a correlation between the capability of MXene-based Fe nanocomposites to electrochemically reduce hydrogen peroxide and electrochemical activity of Fe species present on MXenes. The highest electrochemical current density obtained for H2O2 reduction was obtained on the Ti3C2Tx MXene-based Fe nanocomposite with the value of 4399 µA cm−2. We further discuss how to improve the current density obtained for H2O2 reduction on the other MXene-based Fe nanocomposites (Nb2CTx and Nb4C3Tx) using alternative synthesis protocols.

Original languageEnglish
Pages (from-to)15204-15215
Number of pages12
JournalRSC Advances
Volume16
Issue number17
DOIs
Publication statusPublished - 19 Mar 2026

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