A new
atomic-scale anisotropy in the photoreaction of surface carboxylates
on rutile TiO2(110) induced by gold clusters is found.
STM and DFT+U are used to study this phenomenon by monitoring the
photoreaction of a prototype hole-scavenger molecule, benzoic acid,
over stoichiometric (s) s-TiO2, Au9/s-TiO2, and reduced (r) Au9/r-TiO2. STM results
show that benzoic acid adsorption displaces a large fraction of Au
clusters from the terraces toward their edges. DFT calculations explain
that Au9 clusters on stoichiometric TiO2 are
distorted by benzoic acid adsorption. The influence of sub-monolayers
of Au on the UV/visible photoreaction of benzoic acid was explored
at room temperature, with adsorbate depletion taken as a measure of
activity. The empty sites, observed upon photoexcitation, occurred
in elongated chains (2 to 6 molecules long) in the [11̅0] and
[001] directions. A roughly 3-fold higher depletion rate is observed
in the [001] direction. This is linked to the anisotropic conduction
of excited electrons along [001], with subsequent trapping by Au clusters
leaving a higher concentration of holes and thus an increased decomposition
rate. To our knowledge this is the first time that atomic-scale directionality
of a chemical reaction is reported upon photoexcitation of the semiconductor.
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