Role of side groups in pyridine and bipyridine ruthenium dye complexes for modulated surface photovoltage in nanoporous TiO2
dc.contributor.author | Sahin, C. | |
dc.contributor.author | Dittrich, Th. | |
dc.contributor.author | Varlikli, C. | |
dc.contributor.author | Icli, S. | |
dc.contributor.author | Lux-Steiner, M. Ch. | |
dc.date.accessioned | 2019-10-27T21:18:31Z | |
dc.date.available | 2019-10-27T21:18:31Z | |
dc.date.issued | 2010 | |
dc.department | Ege Üniversitesi | en_US |
dc.description | Symposium on Mesoscopic Dye Sensitized and Organic Heterojunction Solar Cells held at the e-MRS 2009 Spring Meeting -- 2009 -- Strasbourg, FRANCE | en_US |
dc.description.abstract | The influence of molecular side groups on the electron backtransfer into ruthenium-dye molecules adsorbed on ultra-thin nanoporous TiO2 layers has been investigated by modulated surface photovoltage spectroscopy in argon atmosphere. All ruthenium-dye molecules contained one bipyridine (bpy) ligand with two carboxylic groups for anchoring at the TiO2 surface. Ruthenium (II) complexes with a second bpy ligand with branching and non-branching side groups containing C and H only and ruthenium (II) complexes with a second pyridine (py) ligand with side groups containing different numbers of -C-O-C- sequences were synthesized. The electron backtransfer was practically not affected by branching or non-branching side groups in the bpy-bpy complexes. In contrast, electron backtransfer was much less for bpy-py complexes in comparison to bpy-bpy complexes and increased strongly with increasing number of -C-O-C- sequences in the side groups. (C) 2009 Elsevier B.V. All rights reserved. | en_US |
dc.description.sponsorship | E-MRS | en_US |
dc.identifier.doi | 10.1016/j.solmat.2009.11.008 | |
dc.identifier.endpage | 690 | en_US |
dc.identifier.issn | 0927-0248 | |
dc.identifier.issn | 0927-0248 | en_US |
dc.identifier.issue | 4 | en_US |
dc.identifier.startpage | 686 | en_US |
dc.identifier.uri | https://doi.org/10.1016/j.solmat.2009.11.008 | |
dc.identifier.uri | https://hdl.handle.net/11454/43995 | |
dc.identifier.volume | 94 | en_US |
dc.identifier.wos | WOS:000276718500010 | en_US |
dc.identifier.wosquality | Q1 | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.language.iso | en | en_US |
dc.publisher | Elsevier Science Bv | en_US |
dc.relation.ispartof | Solar Energy Materials and Solar Cells | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Ruthenium (II) complex | en_US |
dc.subject | Surface photovoltage spectroscopy | en_US |
dc.subject | Electron backtransfer | en_US |
dc.subject | Titanium dioxide | en_US |
dc.title | Role of side groups in pyridine and bipyridine ruthenium dye complexes for modulated surface photovoltage in nanoporous TiO2 | en_US |
dc.type | Article | en_US |