The adsorption and reactions of SiCl x (x=0-4) on hydroxylated TiO 2 anatase (101) surface: A computational study on the functionalization of titania with Cl 2Si(O)O adsorbate

Wen Fei Huang, Hsin Tsung Chen*, Ming-Chang Lin

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

9 Scopus citations

Abstract

The adsorption and reactions of the SiCl x (x=0-4) on the hydroxylated TiO 2 anatase (101) surface have been investigated by using periodic density functional theory calculations in conjunction with the projected augmented wave (PAW) approach. The adsorption and reactions tend to occur more readily on the 'O w' site derived from water than the 'O s' site from TiO 2 as revealed by the potential energy profiles and adsorption energies. The stepwise reactions of SiCl x can be achieved by dehydrochlorination taking place by three paths: O w-path, cross-path, and O s-path. The O w-path is the lowest energy path, in which Cl 3Si-O w(a) and Cl 2Si-(O w)O w(a) are the main products formed by spontaneous reactions. The ready formation and the high stability of Cl 2Si-(O w)O w(a) suggest that it can be employed as a molecular linker for Si and other semiconductor quantum dot growth on titania through its high reactivity towards SiH x radicals and metal alkyls, respectively.

Original languageEnglish
Pages (from-to)45-52
Number of pages8
JournalComputational and Theoretical Chemistry
Volume993
DOIs
StatePublished - 1 Aug 2012

Keywords

  • Density functional theory
  • Hydroxylated TiO
  • SiCl adsorption

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