uu.seUppsala University Publications
Change search
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf
Influence of Dye Architecture of Triphenylamine Based Organic Dyes on the Kinetics in Dye-Sensitized Solar Cells
Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry - Ångström, Physical Chemistry.
Carl von Ossietzky Univ Oldenburg, Inst Chem, Ctr Interface Sci, Fac Math & Nat Sci, D-26111 Oldenburg, Germany..
Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry - Ångström, Physical Chemistry. Ecole Polytech Fed Lausanne, Inst Chem Sci & Engn, Lab Photomol Sci, EPFL FSB ISIC LSPM, CH-1015 Lausanne, Switzerland.;King Abdulaziz Univ, Ctr Excellence Adv Mat Res, Jeddah 21589, Saudi Arabia..
Carl von Ossietzky Univ Oldenburg, Inst Chem, Ctr Interface Sci, Fac Math & Nat Sci, D-26111 Oldenburg, Germany..
Show others and affiliations
2015 (English)In: The Journal of Physical Chemistry C, ISSN 1932-7447, E-ISSN 1932-7455, Vol. 119, no 38, 21775-21783 p.Article in journal (Refereed) Published
Abstract [en]

The impact of the dye architecture on the kinetics in the dyesensitized solar cell (DSC) was investigated for two structurally similar organic dyes, adsorbed adsorbed to a mesoporous TiO2 film. Differences in the HOMO and LUMO levels of the triphenylamine dyes D35 and D45 were negligible, indicating that the changes in kinetics of the electron transfer processes in the solar cells can be attributed to structural differences of the organic dyes. The electron transfer kinetics of various processes was investigated by scanning electrochemical microscopy (SECM), transient absorption spectroscopy (TAS), and impedance spectroscopy (IS). SECM was used for the first time to determine the rate constants of the regeneration (reduction) of a photooiddized organic dye by a oneelectron cobalt mediator. Both TAS and IS measurements showed differences in recombination of electrons in TiO2, with oxidized D35 and D45. D45 with its shorter dimethoxyphenyl units yielded faster recombination and regeneration than D35, as measured by SECM and TAS. The results of this study show that small details in the dye structure significantly affect the kinetics of organic triphenylamine dye based dye-sensitized solar cells.

Place, publisher, year, edition, pages
2015. Vol. 119, no 38, 21775-21783 p.
National Category
Physical Chemistry
Identifiers
URN: urn:nbn:se:uu:diva-265912DOI: 10.1021/acs.jpcc.5b04436ISI: 000361921600003OAI: oai:DiVA.org:uu-265912DiVA: diva2:867060
Funder
Swedish Energy AgencyKnut and Alice Wallenberg FoundationSwedish Research CouncilStandUp
Available from: 2015-11-04 Created: 2015-11-04 Last updated: 2017-12-01Bibliographically approved
In thesis
1. Developing Environmentally Friendly Dye-sensitized Solar Cells
Open this publication in new window or tab >>Developing Environmentally Friendly Dye-sensitized Solar Cells
2016 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

Due to climate change and its effects, alternative renewable energy sources are needed in the future human society. In the work of this thesis, the Dye-sensitized Solar Cell (DSC) has been investigated and characterized.

DSCs are appealing as energy conversion devices, since they have high potential to provide low cost solar light to electricity conversion. The DSC is built up by a working electrode consisting of a conductive glass substrate with a dye-sensitized mesoporous TiO2 film, a counter electrode with a catalyst and, in between, the electrolyte which performs the charge transport by means of a redox mediator. The aim of this thesis was to develop and evaluate cheap and environmentally friendly materials for the DSC.

An alternative polymer-based counter electrode catalyst was fabricated and evaluated, showing that the PEDOT catalyst counter electrode outperformed the platinum catalyst counter electrode. Different organic dyes were evaluated and it was found that the dye architecture affected the performance of the assembled DSCs. A partly hydrophilic organic triphenylamine dye was developed and applied in water-based electrolyte DSCs. The partly hydrophilic dye outperformed the reference hydrophobic dye. Small changes in dye architecture were evaluated for two similar dyes, both by spectroscopic and electrochemical techniques. A change in the length of the dialkoxyphenyl units on a triphenylamine dye, affected the recombination and the regeneration electron transfer kinetics in the DSC system. Finally, three water soluble cobalt redox couples were developed and applied in water-based electrolyte DSCs. An average efficiency of 5.5% (record efficiency of 5.7%) for a 100% water-based electrolyte DSC was achieved with the polymer-based catalyst counter electrode and an organic dye with short dimethoxyphenyl units, improving the wetting and the regeneration process.

Place, publisher, year, edition, pages
Uppsala: Acta Universitatis Upsaliensis, 2016. 82 p.
Series
Digital Comprehensive Summaries of Uppsala Dissertations from the Faculty of Science and Technology, ISSN 1651-6214 ; 1351
Keyword
dye-sensitized solar cells, dye, cobalt, triphenylamine, titanium dioxide, aqueous, PEDOT
National Category
Physical Chemistry
Research subject
Chemistry with specialization in Physical Chemistry
Identifiers
urn:nbn:se:uu:diva-280291 (URN)978-91-554-9506-0 (ISBN)
Public defence
2016-04-29, Polhemsalen; Ång/10134, Ångströmlaboratoriet, Lägerhyddsvägen 1, Uppsala, 10:15 (English)
Opponent
Supervisors
Available from: 2016-04-06 Created: 2016-03-09 Last updated: 2016-05-24

Open Access in DiVA

No full text

Other links

Publisher's full text

Authority records BETA

Ellis, HannaHagfeldt, AndersBoschloo, Gerrit

Search in DiVA

By author/editor
Ellis, HannaHagfeldt, AndersBoschloo, Gerrit
By organisation
Physical Chemistry
In the same journal
The Journal of Physical Chemistry C
Physical Chemistry

Search outside of DiVA

GoogleGoogle Scholar

doi
urn-nbn

Altmetric score

doi
urn-nbn
Total: 731 hits
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf