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Characterization of the Interface Properties and Processes in Solid State Dye-Sensitized Solar Cells Employing a Perylene Sensitizer
Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Kemiska sektionen, Institutionen för fysikalisk och analytisk kemi, Fysikalisk kemi.
Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Kemiska sektionen, Institutionen för fotokemi och molekylärvetenskap, Kemisk fysik.
Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi, Yt- och gränsskiktsvetenskap.
Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Kemiska sektionen, Institutionen för fysikalisk och analytisk kemi, Fysikalisk kemi.
Vise andre og tillknytning
2011 (engelsk)Inngår i: The Journal of Physical Chemistry C, ISSN 1932-7447, E-ISSN 1932-7455, Vol. 115, nr 10, s. 4345-4358Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

We recently reported on a perylene sensitizer, ID176, which performs much better in solid state dye-sensitized solar cells than in those using liquid electrolytes with iodide/tri-iodide as the redox couple (J. Phys. Chem. C2009, 113, 14595-14597). Here, we present a characterization of the sensitizer and of the TiO2/dye interface by UV-visible absorption and fluorescence spectroscopy, spectroelectrochemistry, photoelectron spectroscopy, electroabsorption spectroscopy, photoinduced absorption spectroscopy, and femtosecond transient absorption measurements. We report that the absorption spectrum of the sensitizer is red-shifted by addition of lithium ions to the surface due to a downward shift of the excited state level of the sensitizer, which is of the same order of magnitude as the downward shift of the titanium dioxide conduction band edge. Results from photoelectron spectroscopy and electrochemistry suggest that the excited state is largely located below the conduction band edge of TiO2 but that there are states in the band gap of TiO2 which might be available for photoinduced electron injection. The sensitizer was able to efficiently inject into TiO2, when a lithium salt was present on the surface, while injection was much less effective in the absence of lithium ions or in the presence of solvent. In the presence of the hole conductor 2,2-,7,7-tetrakis-(N,N-di-p-methoxyphenyl-amine)-9,9-spirobifluorene (spiro-MeOTAD) and LiTFSI, charge separation was monitored by the emergence of a Stark shift of the dye in transient absorption spectra, and both injection and regeneration appear to be completed within 1 ps. Regeneration by spiro-MeOTAD is therefore several orders of magnitude faster than regeneration by iodide, and ID176 can even be photoreduced by spiro-MeOTAD.

sted, utgiver, år, opplag, sider
2011. Vol. 115, nr 10, s. 4345-4358
HSV kategori
Forskningsprogram
Fysikalisk kemi
Identifikatorer
URN: urn:nbn:se:uu:diva-149013DOI: 10.1021/jp111466hISI: 000288113400064OAI: oai:DiVA.org:uu-149013DiVA, id: diva2:403617
Tilgjengelig fra: 2011-03-14 Laget: 2011-03-14 Sist oppdatert: 2017-12-11bibliografisk kontrollert
Inngår i avhandling
1. Characterisation of Organic Dyes for Solid State Dye-Sensitized Solar Cells
Åpne denne publikasjonen i ny fane eller vindu >>Characterisation of Organic Dyes for Solid State Dye-Sensitized Solar Cells
2011 (engelsk)Doktoravhandling, med artikler (Annet vitenskapelig)
Abstract [en]

Energy from the sun can be converted to low cost electricity using dye-sensitized solar cells (DSCs). Dye molecules adsorbed to the surface of mesoporous TiO2 absorb light and inject electrons into the semiconductor. They are then regenerated by the reduced redox species from an electrolyte, typically consisting of the iodide/tri-iodide redox couple in an organic solvent. In a solid state version of the DSC, the liquid electrolyte is replaced by an organic hole conductor. Solid state DSCs using 2,2'7,7'-tetrakis-(N,N-di-p-methoxyphenyl-amine)-9,9'-spirobifluorene (spiro-MeOTAD) have reached conversion efficiencies of up to 6 %, which is about half of the efficiency of the best iodide/tri-iodide cells.

 

Measurement techniques, such as spectroelectrochemistry and photo-induced absorption spectroscopy (PIA), were developed and applied to study the working mechanism of organic dyes in solid state DSCs under solar cell operating conditions. The energy alignment of the different solar cell components was studied by spectroelectrochemistry and the results were compared to photoelectron spectroscopy. PIA was used to study the injection and regeneration processes. For the first time, it was shown here that the results of PIA are influenced by an electric field due to the electrons injected into the TiO2. This electric field causes a shift in the absorption spectrum of dye molecules adsorbed to the TiO2 surface due to the Stark effect.

 

Taking the Stark effect into consideration during the data analysis, mechanistic differences between solid state and conventional DSCs were found. A perylene dye, ID176, was only able to efficiently inject electrons into the TiO2 in presence of lithium ions and in absence of a solvent. As a result, the sensitiser worked surprisingly well in solid state DSCs but not in liquid electrolyte ones. Regeneration of oxidised dye molecules by spiro-MeOTAD was found to be fast and efficient and spiro-MeOTAD could even reduce excited dye molecules.

sted, utgiver, år, opplag, sider
Uppsala: Acta Universitatis Upsaliensis, 2011. s. 89
Serie
Digital Comprehensive Summaries of Uppsala Dissertations from the Faculty of Science and Technology, ISSN 1651-6214 ; 814
Emneord
energy alignment, hole conductor, injection, interface, perylene, photo-induced absorption, regeneration, spectroelectrochemistry, spiro-MeOTAD, Stark effect, titanium dioxide
HSV kategori
Forskningsprogram
Fysikalisk kemi
Identifikatorer
urn:nbn:se:uu:diva-150047 (URN)978-91-554-8042-4 (ISBN)
Disputas
2011-05-13, Häggsalen, Ångströmlaboratoriet, Lägerhyddsvägen 1, Uppsala, 10:00 (engelsk)
Opponent
Veileder
Tilgjengelig fra: 2011-04-20 Laget: 2011-03-25 Sist oppdatert: 2011-05-04bibliografisk kontrollert

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