4.6 Article

TiO2-Catalyzed Photodegradation of Porphyrins: Mechanistic Studies and Application in Monolayer Photolithography

Journal

LANGMUIR
Volume 25, Issue 9, Pages 5398-5403

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/la804256f

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Funding

  1. National Science Foundation [CHE-0645678]
  2. University at Buffalo, State University of New York

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Patterned mixed monolayers of porphyrins on nanocrystalline TiO2 films were fabricated by substrate-catalyzed monolayer photolithography. Tin(IV) protoporphyrin IX (SnPP), zinc(II) protoporphyrin IX (ZnPP), and iron(III) meso-tetra(4-carboxyphenyl)porphine (FeTCP) were adsorbed to TiO2 through the carboxyl groups, yielding saturation surface amounts per projected area of approximately 10(-7) Mol/cm(2). Illumination of SnPP- and ZnPP-functionalized TiO2 films with 355 nm light caused the desorption of the porphyrins, most likely through oxidative decarboxylation. SnPP was removed more rapidly than ZnPP. The faster kinetics was due, in part, to the contribution of other photochemical pathways including TiO2-catalyzed photoreduction and direct photodegradation reactions. Patterned binary monolayers were prepared by the photoinduced desorption of a protoporphyrin, followed by the adsorption of FeTCP to previously illuminated regions of the surface.

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