Electronic properties of the interface between p-CuI and anatase-phase n-Ti O2 single crystal and nanoparticulate surfaces: A photoemission study

Research output: Contribution to journalArticle

  • External authors:
  • A. R. Kumarasinghe
  • A. K. Mallick
  • D. Tsoutsou
  • C. Chatwin
  • S. Rayner
  • P. Kirkham
  • S. Warren
  • S. Patel
  • P. Christian
  • P. O'Brien
  • M. Grätzel
  • R. Hengerer

Abstract

We present a study of the growth of the p -type inorganic semiconductor CuI on n -type Ti O2 anatase single crystal (101) surfaces and on nanoparticulate anatase surfaces using synchrotron radiation photoemission spectroscopy. Core level photoemission data obtained using synchrotron radiation reveal that both the substrate (Ti O2) and the overlayer (CuI) core levels shift to a lower binding energy to different degrees following the growth of CuI on Ti O2. Valence band photoemission data show that the valence band maximum of the clean substrate differs from that of the dosed surface which may be interpreted qualitatively as due to the introduction of a new density of states within the band gap of Ti O2 as a result of the growth of CuI. The valence band offset for the heterojunction n-Ti O2 p-CuI has been measured using photoemission for both nanoparticulate and single crystal Ti O2 surfaces, and the band energy alignment for these heterojunction interfaces is presented. With the information obtained here, it is suggested that the interface between p-CuI and single crystal anatase-phase n-Ti O2 is a type-II heterojunction interface, with significant band bending. The measured total band bending matches the work function change at the interface, i.e., there is no interface dipole. In the case of the nanoparticulate interface, an interface dipole is found, but band bending within the anatase nanoparticles remains quite significant. We show that the corresponding depletion layer may be accommodated within the dimension of the nanoparticles. The results are discussed in the context of the functional properties of dye-sensitized solid state solar cells. © 2007 American Institute of Physics.

Bibliographical metadata

Original languageEnglish
Article number114703
JournalJournal of Chemical Physics
Volume127
Issue number11
DOIs
Publication statusPublished - 2007