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dc.contributor.authorHsiao, Yu-Shengen_US
dc.contributor.authorWhang, Wha-Tzongen_US
dc.contributor.authorChen, Chih-Pingen_US
dc.contributor.authorChen, Yi-Chunen_US
dc.date.accessioned2014-12-08T15:12:50Z-
dc.date.available2014-12-08T15:12:50Z-
dc.date.issued2008en_US
dc.identifier.issn0959-9428en_US
dc.identifier.urihttp://hdl.handle.net/11536/9887-
dc.identifier.urihttp://dx.doi.org/10.1039/b813079een_US
dc.description.abstractIn this study, we devised a simple method to enhance the conductivity of poly(3,4-ethylenedioxythiophene)-poly(styrene-sulfonate) (PEDOT:PSS) films through spin-coating with various surface-modified compounds, and then applied this technique to the preparation of ITO-free polymer solar cells (PSCs). The electrical conductivity of PEDOT: PSS films can be increased by more than two order of magnitudes merely by spin-coating a compound containing one or more polar groups - such as ethanol, methoxyethanol, 1,2-dimethoxyethane, and ethylene glycol - onto the films. In this paper, we discuss the phenomena occurring through conductivities, morphologies, and chemical properties of the modified PEDOT-PSS films as determined using Raman spectroscopy, a four-point probe, scanning electron microscopy (SEM), atomic force microscopy (AFM), transmission electron microscopy (TEM), and X-ray photoelectron spectroscopy (XPS). The schematic 3D morphological model of directly solvent-modified PEDOT: PSS films is presumed for ITO-free devices. The desirable conductivity enhancements of these materials make them attractive candidates for use as anode materials in ITO-free PSCs.en_US
dc.language.isoen_USen_US
dc.titleHigh-conductivity poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) film for use in ITO-free polymer solar cellsen_US
dc.typeArticleen_US
dc.identifier.doi10.1039/b813079een_US
dc.identifier.journalJOURNAL OF MATERIALS CHEMISTRYen_US
dc.citation.volume18en_US
dc.citation.issue48en_US
dc.citation.spage5948en_US
dc.citation.epage5955en_US
dc.contributor.department材料科學與工程學系zh_TW
dc.contributor.departmentDepartment of Materials Science and Engineeringen_US
dc.identifier.wosnumberWOS:000261745700012-
dc.citation.woscount60-
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