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J. Chem. Phys. 134, 054705 (2011); http://dx.doi.org/10.1063/1.3549573 (10 pages)

Charge transfer dynamics of model charge transfer centers of a multicenter water splitting dye complex on rutile TiO2(110)

Matthew Weston, Andrew J. Britton, and James N. O’Shea

School of Physics and Astronomy, and Nottingham Nanotechnology and Nanoscience Centre (NNNC), University of Nottingham, Nottingham NG7 2RD, United Kingdom

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(Received 12 October 2010; accepted 11 January 2011; published online 2 February 2011)

Charge transfer dynamics between an adsorbed molecule and a rutile TiO2(110) surface have been investigated in three organometallic dyes related to multicenter water splitting dye complexes: Ru 535 (cis-bis(isothiocyanato)bis(2,2-bipyridyl-4,4-dicarboxylato)-ruthenium(II)), Ru 455 (cis-bis(2,2-bipyridyl)-(2,2-bipyridyl-4,4-dicarboxylic acid)-ruthenium(II)), and Ru 470 (tris(2,2-bipyridyl-4,4-dicarboxylic acid)-ruthenium(II)). The adsorption of the dye molecules on the rutile TiO2(110) surface has been studied using core-level and valence photoemission. Dye molecules were deposited in situ using ultrahigh vacuum electrospray deposition. Core-level photoemission spectra reveal that each complex bonds to the surface via deprotonation of two carboxylic groups. All three dye complexes show evidence of ultrafast charge transfer to the TiO2 substrate using the core-hole clock implementation of resonant photoemission spectroscopy.

© 2011 American Institute of Physics

Article Outline

  1. INTRODUCTION
  2. METHOD
  3. RESULTS AND DISCUSSION
    1. Adsorption
    2. Electronic structure
    3. Charge transfer dynamics
  4. CONCLUSIONS

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KEYWORDS and PACS

PACS

  • 68.43.-h

    Chemisorption/physisorption: adsorbates on surfaces

  • 81.15.Pq

    Electrodeposition, electroplating

ARTICLE DATA

PUBLICATION DATA

ISSN

0021-9606 (print)  
1089-7690 (online)

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