4.8 Article

Molecular Imaging of Reductive Coupling Reactions: Interstitial-Mediated Coupling of Benzaldehyde on Reduced TiO2(110)

Journal

ACS NANO
Volume 5, Issue 2, Pages 834-843

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/nn103144u

Keywords

scanning tunneling microscopy; density functional theory; titanium dioxide; benzaldehyde; interstitial; oxygen vacancy

Funding

  1. Chemistry Division of the National Science Foundation [CHE-0545335]
  2. A. v. Humboldt foundation
  3. NSF
  4. Division Of Chemistry
  5. Direct For Mathematical & Physical Scien [0956653] Funding Source: National Science Foundation

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We report the first visualization of a reactive intermediate formed from coupling two molecules on a surface-a diolate formed from benzaldehyde coupling on TiO2(110). The diolate, imaged using scanning tunneling microscopy (STM), is reduced to gaseous stilbene upon heating to similar to 400 K, leaving behind two oxygen atoms that react with reduced Ti interstitials that migrate to the surface, contrary to the popular expectation that strong bonds in oxygenated molecules react only with oxygen vacancies at the surface. Our work further provides both experimental and theoretical evidence that Ti interstitials drive the formation of diolate intermediates. Initially mobile monomers migrate together to form paired features, identified as diolates that bond corer two adjacent five-coordiante Ti atoms on the surface. Our work is of broad importance because it demonstrates the possibility of imaging the distribution and bonding configurations of reactant species on a molecular scale, which is a critical part of understanding surface reactions and the development of surface morphology during the course of reaction.

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