Highly Conductive PEDOT:PSS Electrode with Optimized Solvent and Thermal Post-Treatment for ITO-Free Organic Solar Cells
Highly conductive poly(3,4‐ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) films as stand‐alone electrodes for organic solar cells have been optimized using a solvent post‐treatment method. The treated PEDOT:PSS films show enhanced conductivities up to 1418 S cm−1, accompanied by structur...
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Veröffentlicht in: | Advanced functional materials 2011-03, Vol.21 (6), p.1076-1081 |
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Sprache: | eng |
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Zusammenfassung: | Highly conductive poly(3,4‐ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) films as stand‐alone electrodes for organic solar cells have been optimized using a solvent post‐treatment method. The treated PEDOT:PSS films show enhanced conductivities up to 1418 S cm−1, accompanied by structural and chemical changes. The effect of the solvent treatment on PEDOT:PSS has been investigated in detail and is shown to cause a reduction of insulating PSS in the conductive polymer layer. Using these optimized electrodes, ITO‐free, small molecule organic solar cells with a zinc phthalocyanine (ZnPc):fullerene C60 bulk heterojunction have been produced on glass and PET substrates. The system was further improved by pre‐heating the PEDOT:PSS electrodes, which enhanced the power conversion efficiency to the values obtained for solar cells on ITO electrodes. The results show that optimized PEDOT:PSS with solvent and thermal post‐treatment can be a very promising electrode material for highly efficient flexible ITO‐free organic solar cells.
Highly conductive PEDOT:PSS films [PEDOT:PSS = poly(3,4‐ethylenedioxythiophene):poly(styrenesulfonate)] have been optimized by a solvent and thermal post‐treatment method, and applied as an electrode for small‐molecule organic solar cells with a ZnPc:C60 bulk heterojunction. The solar cell with the optimized PEDOT:PSS electrode can reach an efficiency of 2.54%, as high as that of a solar cell with indium tin oxide (ITO) electrode. |
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ISSN: | 1616-301X 1616-3028 |
DOI: | 10.1002/adfm.201002290 |