Photoelectrochemistry with integrated photosensitizer-electron acceptor and Au-nanoparticle arrays

Citation
M. Lahav et al., Photoelectrochemistry with integrated photosensitizer-electron acceptor and Au-nanoparticle arrays, J AM CHEM S, 122(46), 2000, pp. 11480-11487
Citations number
44
Categorie Soggetti
Chemistry & Analysis",Chemistry
Journal title
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
ISSN journal
00027863 → ACNP
Volume
122
Issue
46
Year of publication
2000
Pages
11480 - 11487
Database
ISI
SICI code
0002-7863(20001122)122:46<11480:PWIPAA>2.0.ZU;2-B
Abstract
Photosensitizer/electron acceptor molecular cross-linked Au-nanoparticle ar rays are assembled on indium-doped tin oxide (ITO) electrodes by a layer-by -layer deposition process. A Ru(II)-tris-(2, 2'-bipyridine)cyclobis(paraqua t-p-phenylene) catenane (1) or Zn(II)-protoporphyrin IX-bis(N-methyl-N'-und ecanoate-4,4'-bipyridinium) (2) are used as molecular cross-linkers for the generation of Au-nanoparticle (13 +/- 1 nm) arrays of a controlled number of layers. The Au-nanoparticle arrays are characterized by absorbance spect roscopy and by electrochemical means. The electrodes functionalized with 1- or 2-cross-linked Au-nanoparticle arrays are used in photoelectrochemical experiments. The resulting action spectra of the photocurrents follow the a bsorbance spectra of the respective chromophores. Mechanistic studies indic ate that the photocurrents originate from intramolecular electron-transfer quenching of the photoexcited state of the photosensitizer by the electron acceptor units, leading to the formation of intermediate redox species. The oxidized photoproduct oxidizes the sacrificial electron donor, Na(2)EDTA, whereas the reduced bipyridinium radical cations transfer the electrons to the bulk electrode support.