Published December 2011 | Version v1
Journal article

Colloidal nanocrystal ZnO- and TiO2-modified electrodes sensitized with chlorophyll a and carotenoids: a photoelectrochemical study

  • 1. Politecnico di Bari, Dipartimento di Ingegneria delle Acque e di Chimica (Italy)
  • 2. Università di Bari "Aldo Moro", Dipartimento di Chimica (Italy)
  • 3. Università di Bari, Istituto per i Processi Chimico Fisici Consiglio Nazionale delle Ricerche (CNR IPCF), c/o Dip. Chimica (Italy)

Description

Heterostructures formed of films of organic-capped ZnO and TiO2 nanocrystals (both with the size of ca. 6 nm) and photosynthetic pigments were prepared and characterized. The surface of optically transparent electrodes (Indium Tin Oxide) was modified with nanocrystals and prepared by colloidal synthetic routes. The nanostructured electrodes were sensitized by a mixture of chlorophyll a and carotenoids. The characterization of the hybrid structures, carried out by means of steady-state optical measurements, demonstrated such class of dyes able to extend the photoresponse of the large band-gap semiconductors. The charge-transfer processes between the components of the heterojunction were investigated, and photoelectrochemical measurements taken on the sensitized ZnO and TiO2 nanocrystals electrodes elucidated the photoactivity of the heterojunctions as a function of the dyes and of the red–ox mediator used in solution. The effect of methyl viologen as different red–ox mediator was also evaluated in order to show its effect on the heterojunction photoactivity. The overall results contributed to describe the photoelectrochemical potential of the investigated heterojunctions, highlighting a higher response of the dye-sensitized ZnO nanocrystals, and then provided the TiO2-modified counterparts.

Additional details

Identifiers

Publishing Information

Journal Title
Journal of Nanoparticle Research
Journal Volume
13
Journal Issue
12
Journal Page Range
p. 6467-6481
ISSN
1388-0764

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Copyright (c) 2011 Springer Science+Business Media B.V.