<div class="csl-bib-body">
<div class="csl-entry">Balajka, J., Hines, M. A., DeBenedetti, W. J. I., Komora, M., Pavelec, J., Schmid, M., & Diebold, U. (2018). High-affinity adsorption leads to molecularly ordered interfaces on TiO₂ in air and solution. <i>Science</i>, <i>361</i>, 786–789. https://doi.org/10.1126/science.aat6752</div>
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dc.identifier.issn
0036-8075
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dc.identifier.uri
http://hdl.handle.net/20.500.12708/145271
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dc.description.abstract
Researchers around the world have observed the formation of molecularly ordered
structures of unknown origin on the surface of titanium dioxide (TiO2) photocatalysts
exposed to air and solution. Using a combination of atomic-scale microscopy and
spectroscopy, we show that TiO2 selectively adsorbs atmospheric carboxylic acids that are
typically present in parts-per-billion concentrations while effectively repelling other
adsorbates, such as alcohols, that are present in much higher concentrations. The high
affinity of the surface for carboxylic acids is attributed to their bidentate binding.
These self-assembled monolayers have the unusual property of being both hydrophobic
and highly water-soluble, which may contribute to the self-cleaning properties of TiO2.
This finding is relevant to TiO2 photocatalysis, because the self-assembled carboxylate
monolayers block the undercoordinated surface cation sites typically implicated
in photocatalysis.
en
dc.language.iso
en
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dc.relation.ispartof
Science
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dc.title
High-affinity adsorption leads to molecularly ordered interfaces on TiO₂ in air and solution