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Size Dependence of Electrical Conductivity and Thermoelectric Enhancements in Spin-Coated PEDOT:PSS Single and Multiple Layers

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Beeg,  Sebastian
Department of Heterogeneous Reactions, Max-Planck-Institute for Chemical Energy Conversion;
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Knop-Gericke,  Axel
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Fulltext (public)

AdvElectronMater-2016-2.pdf
(Any fulltext), 666KB

Supplementary Material (public)

aelm201600473-sup-0001-S1.pdf
(Supplementary material), 2MB

Citation

Andrei, V., Bethke, K., Madzharova, F., Beeg, S., Knop-Gericke, A., Kneipp, J., et al. (2017). Size Dependence of Electrical Conductivity and Thermoelectric Enhancements in Spin-Coated PEDOT:PSS Single and Multiple Layers. Advanced Electronic Materials, 3(2): 1600473. doi:10.1002/aelm.201600473.


Cite as: https://hdl.handle.net/11858/00-001M-0000-002C-9190-0
Abstract
This work reveals that the electrical conductivity σ of a poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) film can be significantly increased by spin-coating multiple thin layers onto a substrate. Generally, σ can be improved by more than fourfold for multiple layers, as compared to a single thicker one. A gradual enhancement is observed for pristine PEDOT:PSS films (up to 2.10 ± 0.26 S cm–1 for five-layered films), while a plateau in σ at around 200 S cm–1 is reached after only three layers, when using a PEDOT:PSS solution with 5 vol% dimethyl sulfoxide. By contrast, only a small change in σ is observed for single layers of varying thickness. Accordingly, the thermoelectric power factor is also increased by up to 3.4 times for the multiple layers. Based on atomic force microscopy, X-ray photoelectron spectroscopy, UV–vis, and Raman spectroscopy measurements, two mechanisms are also proposed, involving an increase in percolation by inclusion of smaller grains within the existing ones, respectively, a reorganization of the PEDOT:PSS chains. These findings represent a direct strategy for enhancing the thermoelectric performance of conductive polymer films without additional reagents, while the mechanistic insights explain existing literature results.