Abstract
An investigation of five ruthenium complexes with the thermodynamics and kinetics of binding to nanocrystalline TiO2 was made. The ruthenium complexes were structurally different in the number of anchoring carboxy groups attached to coordinated bipyridyl ligands and in the number of auxillary ligands. All the available carboxyl groups were used by the complexes in the dry state with only one monocarboxy or dicarboxy ligand to bind to the surface. The structural difference between the complexes in the five dyes yielded similar maximum coverages ( >100nmol cm-2) on nanocrystalline TiO2 electrodes and exhibited different binding constants.
| Original language | English |
|---|---|
| Pages (from-to) | 15640-15651 |
| Number of pages | 12 |
| Journal | Journal of Physical Chemistry B |
| Volume | 108 |
| Issue number | 40 |
| DOIs | |
| Publication status | Published - Oct 7 2004 |
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ASJC Scopus subject areas
- Physical and Theoretical Chemistry
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Anchoring group and auxiliary ligand effects on the binding of ruthenium complexes to nanocrystalline TiO2 photoelectrodes. / Kilså, Kristine; Mayo, Elizabeth I.; Brunschwig, Bruce S.; Gray, Harry B.; Lewis, Nathan S; Winkler, Jay R.
In: Journal of Physical Chemistry B, Vol. 108, No. 40, 07.10.2004, p. 15640-15651.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Anchoring group and auxiliary ligand effects on the binding of ruthenium complexes to nanocrystalline TiO2 photoelectrodes
AU - Kilså, Kristine
AU - Mayo, Elizabeth I.
AU - Brunschwig, Bruce S.
AU - Gray, Harry B.
AU - Lewis, Nathan S
AU - Winkler, Jay R.
PY - 2004/10/7
Y1 - 2004/10/7
N2 - An investigation of five ruthenium complexes with the thermodynamics and kinetics of binding to nanocrystalline TiO2 was made. The ruthenium complexes were structurally different in the number of anchoring carboxy groups attached to coordinated bipyridyl ligands and in the number of auxillary ligands. All the available carboxyl groups were used by the complexes in the dry state with only one monocarboxy or dicarboxy ligand to bind to the surface. The structural difference between the complexes in the five dyes yielded similar maximum coverages ( >100nmol cm-2) on nanocrystalline TiO2 electrodes and exhibited different binding constants.
AB - An investigation of five ruthenium complexes with the thermodynamics and kinetics of binding to nanocrystalline TiO2 was made. The ruthenium complexes were structurally different in the number of anchoring carboxy groups attached to coordinated bipyridyl ligands and in the number of auxillary ligands. All the available carboxyl groups were used by the complexes in the dry state with only one monocarboxy or dicarboxy ligand to bind to the surface. The structural difference between the complexes in the five dyes yielded similar maximum coverages ( >100nmol cm-2) on nanocrystalline TiO2 electrodes and exhibited different binding constants.
UR - http://www.scopus.com/inward/record.url?scp=6044274487&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=6044274487&partnerID=8YFLogxK
U2 - 10.1021/jp0369995
DO - 10.1021/jp0369995
M3 - Article
AN - SCOPUS:6044274487
VL - 108
SP - 15640
EP - 15651
JO - Journal of Physical Chemistry B Materials
JF - Journal of Physical Chemistry B Materials
SN - 1520-6106
IS - 40
ER -