High thermoelectric power factor from multilayer solution-processed organic films

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 m...

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Bibliographic Details
Main Authors: Zuo, Guangzheng (Author) , Andersson, Olof (Author) , Abdalla, Hassan (Author) , Kemerink, Martijn (Author)
Format: Article (Journal)
Language:English
Published: 21 February 2018
In: Applied physics letters
Year: 2018, Volume: 112, Issue: 8
ISSN:1077-3118
DOI:10.1063/1.5016908
Online Access:Verlag, Volltext: https://doi.org/10.1063/1.5016908
Verlag, Volltext: https://aip.scitation.org/doi/10.1063/1.5016908
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Author Notes:Guangzheng Zuo, Olof Andersson, Hassan Abdalla, and Martijn Kemerink
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Summary: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 (∼25 nm), we achieve a high power factor around 8 μW/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 ∼300 S/m and ∼5 μW/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.
Item Description:Gesehen am 27.11.2019
Physical Description:Online Resource
ISSN:1077-3118
DOI:10.1063/1.5016908