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Hydrogenation of Pt/TiO2{101} nanobelts: A driving force for the improvement of methanol catalysis

  • Feila Liu
  • , Peng Xiao
  • , Wei Quan Tian
  • , Ming Zhou
  • , Yanhong Li
  • , Xun Cui
  • , Yunhuai Zhang*
  • , Xin Zhou
  • *Corresponding author for this work
  • Chongqing University

Research output: Contribution to journalArticlepeer-review

Abstract

Single-crystalline anatase TiO2 nanobelts with a dominant surface of the {101} facet were hydrogenated and used as substrates of platinum for methanol oxidation reaction (MOR). The hydrogenated TiO2 anatase{101} supporting Pt exhibits a 228% increase of current density for methanol oxidation compared with the same system without hydrogenation under dark conditions. The synergetic interactions of hydrogenated anatase{101} with the Pt cluster were investigated through first principles calculations, and found that the hydrogenation shifts the conduction band minimum to the Fermi level of pristine TiO2, and reduces the activation barrier for methanol dissociation considerably. Thus, this work provides an experimental and theoretical basis for developing non-carbon substrates with high electro-catalytic activity toward MOR.

Original languageEnglish
Pages (from-to)28626-28634
Number of pages9
JournalPhysical Chemistry Chemical Physics
Volume17
Issue number43
DOIs
StatePublished - 2015

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