Mechanisms of Reactions Induced by Photocatalysis of Titanium Dioxide Nanoparticles

Joseph Rabani*, Sara Goldstein

*Corresponding author for this work

Research output: Chapter in Book/Report/Conference proceedingChapterpeer-review

3 Scopus citations

Abstract

Photochemical reactions induced by TiO2 nanoparticles share common mechanistic features where electron and hole pairs are formed, migrate to the surface, and their recombination competes with their reaction with various substrates. The main interest in TiO2 photocatalysis is related to its potential application for decontamination of water and air. However, the absorption of TiO2, which is limited to UV light, does not enable the use of natural or cheap light sources, and therefore tremendous effort has been invested in inducing visible-light activity via modification of TiO2 including doping with nonmetals and metals, surface coating, and bi- and multicomponent assembling. In addition, much research has been carried out to inhibit the electron–hole recombination and enhance the reactions of holes and electrons with substrates. The basic mechanism of bare and modified TiO2 and the main principles of the photocatalytic processes remain similar, although the excitation energy is different and the energies of the electrons and holes and their reaction kinetic parameters may vary. These photocatalytic processes are reviewed and discussed.

Original languageEnglish
Title of host publicationHandbook of Environmental Chemistry
PublisherSpringer Verlag
Pages115-158
Number of pages44
DOIs
StatePublished - 2015

Publication series

NameHandbook of Environmental Chemistry
Volume35
ISSN (Print)1867-979X

Bibliographical note

Publisher Copyright:
© Springer-Verlag Berlin Heidelberg 2013.

Keywords

  • Bilayers
  • Composites
  • Doping
  • Electron–hole recombination
  • Graphene
  • Surface modification
  • TiO

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