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Andersson, Olof
Publications (2 of 2) Show all publications
Zuo, G., Andersson, O., Abdalla, H. & Kemerink, M. (2018). High thermoelectric power factor from multilayer solution-processed organic films. Applied Physics Letters, 112(8), Article ID 083303.
Open this publication in new window or tab >>High thermoelectric power factor from multilayer solution-processed organic films
2018 (English)In: Applied Physics Letters, ISSN 0003-6951, E-ISSN 1077-3118, Vol. 112, no 8, article id 083303Article in journal (Refereed) Published
Abstract [en]

We investigate the suitability of the "sequential doping" method of organic semiconductors for thermoelectric applications. The method consists of depositing a dopant (F4TCNQ) containing solution on a previously cast semiconductor (P3HT) thin film to achieve high conductivity, while preserving the morphology. For very thin films (similar to 25 nm), we achieve a high power factor around 8 mu W/mK(-2) with a conductivity over 500 S/m. For the increasing film thickness, conductivity and power factor show a decreasing trend, which we attribute to the inability to dope the deeper parts of the film. Since thick films are required to extract significant power from thermoelectric generators, we developed a simple additive technique that allows the deposition of an arbitrary number of layers without significant loss in conductivity or power factor that, for 5 subsequent layers, remain at similar to 300 S/m and similar to 5 mu W/mK(-2), respectively, whereas the power output increases almost one order of magnitude as compared to a single layer. The efficient doping in multilayers is further confirmed by an increased intensity of (bi)polaronic features in the UV-Vis spectra. Published by AIP Publishing.

Place, publisher, year, edition, pages
AMER INST PHYSICS, 2018
National Category
Materials Chemistry
Identifiers
urn:nbn:se:liu:diva-145764 (URN)10.1063/1.5016908 (DOI)000425977500021 ()
Note

Funding Agencies|China Scholarship Council (CSC); Knut och Alice Wallenbergs stiftelse (Project "Tail of the Sun")

Available from: 2018-03-22 Created: 2018-03-22 Last updated: 2018-05-14
Bergqvist, J., Melianas, A., Andersson, O., Lindqvist, C., Musumeci, C. & Inganäs, O. (2015). Time-resolved morphology formation of solution cast polymer: fullerene blends revealed by in-situ photoluminescence spectroscopy.
Open this publication in new window or tab >>Time-resolved morphology formation of solution cast polymer: fullerene blends revealed by in-situ photoluminescence spectroscopy
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2015 (English)Manuscript (preprint) (Other academic)
Abstract [en]

The nanoscale morphology of the photo-active layer in organic solar cells is critical for device efficiency. The photoactive layer is cast from solution and during drying both the polymer and the fullerene self-assemble to form a blend. Here, we introduce in-situ spectroscopic photoluminescence (PL) combined with laser reflectometry to monitor the drying process of an amorphous polymer:fullerene blend. When casting only the pristine components (polymer or PCBM only), the strength of PL emission is proportional to the solid content of the drying solution, and both kinetics reveal a rapid aggregation onset at the final stage of film drying. On the contrary, when casting polymer:fullerene blends, the strength of PL emission is proportional to the wet film thickness and reveals polymer/fullerene charge transfer (CT) already at the earliest stages of film drying, i.e. in dilute solutions. The proposed method allows to detect polymer/fullerene phase separation during film casting – from a reduction in the PL quenching rate as the film dries. Poor solvents lead to phase separation already at early stages of film drying (low solid content), resulting in a coarse final morphology as confirmed by atomic force microscopy (AFM). We therefore anticipate that the proposed method will be an important tool in the future development of processing inks, not only for solution-cast polymer:fullerene solar cells but also for organic heterojunctions in general.

National Category
Physical Sciences Electrical Engineering, Electronic Engineering, Information Engineering
Identifiers
urn:nbn:se:liu:diva-123032 (URN)
Available from: 2015-12-02 Created: 2015-12-02 Last updated: 2015-12-03
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