Conformational and Electron Dynamics Changes Induced by Cooling Treatment on GO:PEDOT:PSS Transparent Electrodes
Due to issues related to the use of indium, the conjugated polymer poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) is considered as one of the main substitutes for indium tin oxide (ITO) in the structure of organic photovoltaics. Recent works demonstrated that the blend of PEDO...
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Veröffentlicht in: | Journal of physical chemistry. C 2020-12, Vol.124 (49), p.26640-26647 |
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creator | Holakoei, Soheila Veiga, Amanda Garcez Turci, Cássia Curan das Neves, Matheus Felipe Fagundes Wouk, Luana V. Damasceno, João Paulo Zarbin, Aldo J. G Roman, Lucimara S Rocco, Maria Luiza M |
description | Due to issues related to the use of indium, the conjugated polymer poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) is considered as one of the main substitutes for indium tin oxide (ITO) in the structure of organic photovoltaics. Recent works demonstrated that the blend of PEDOT:PSS and graphene oxide (GO) can provide transparent and flexible electrodes with a higher efficiency than PEDOT:PSS itself. In this study, two series of cooled and not-cooled thin films of GO:PEDOT:PSS with different compositions of PEDOT:PSS (1, 5, 10, and 100% (v/v)) were investigated by spectroscopic and morphological techniques to evaluate the effect of the cooling treatment on their electronic and chemical structures, morphology, and carrier mobility. Surface- and bulk-sensitive near-edge X-ray absorption fine structure (NEXAFS) results probed at the sulfur K-edge showed that the cooled GO:PEDOT:PSS 5% blend is the most organized film, which also presented a faster electron delocalization time as probed by resonant Auger spectroscopy using the core-hole clock method. GO:PEDOT:PSS 5% offers the best synergetic effect among the blends, a result which is completely in agreement with electrical results. |
doi_str_mv | 10.1021/acs.jpcc.0c07827 |
format | Article |
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Damasceno, João Paulo ; Zarbin, Aldo J. G ; Roman, Lucimara S ; Rocco, Maria Luiza M</creator><creatorcontrib>Holakoei, Soheila ; Veiga, Amanda Garcez ; Turci, Cássia Curan ; das Neves, Matheus Felipe Fagundes ; Wouk, Luana ; V. Damasceno, João Paulo ; Zarbin, Aldo J. G ; Roman, Lucimara S ; Rocco, Maria Luiza M</creatorcontrib><description>Due to issues related to the use of indium, the conjugated polymer poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) is considered as one of the main substitutes for indium tin oxide (ITO) in the structure of organic photovoltaics. Recent works demonstrated that the blend of PEDOT:PSS and graphene oxide (GO) can provide transparent and flexible electrodes with a higher efficiency than PEDOT:PSS itself. In this study, two series of cooled and not-cooled thin films of GO:PEDOT:PSS with different compositions of PEDOT:PSS (1, 5, 10, and 100% (v/v)) were investigated by spectroscopic and morphological techniques to evaluate the effect of the cooling treatment on their electronic and chemical structures, morphology, and carrier mobility. Surface- and bulk-sensitive near-edge X-ray absorption fine structure (NEXAFS) results probed at the sulfur K-edge showed that the cooled GO:PEDOT:PSS 5% blend is the most organized film, which also presented a faster electron delocalization time as probed by resonant Auger spectroscopy using the core-hole clock method. 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In this study, two series of cooled and not-cooled thin films of GO:PEDOT:PSS with different compositions of PEDOT:PSS (1, 5, 10, and 100% (v/v)) were investigated by spectroscopic and morphological techniques to evaluate the effect of the cooling treatment on their electronic and chemical structures, morphology, and carrier mobility. Surface- and bulk-sensitive near-edge X-ray absorption fine structure (NEXAFS) results probed at the sulfur K-edge showed that the cooled GO:PEDOT:PSS 5% blend is the most organized film, which also presented a faster electron delocalization time as probed by resonant Auger spectroscopy using the core-hole clock method. 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C</addtitle><date>2020-12-10</date><risdate>2020</risdate><volume>124</volume><issue>49</issue><spage>26640</spage><epage>26647</epage><pages>26640-26647</pages><issn>1932-7447</issn><eissn>1932-7455</eissn><abstract>Due to issues related to the use of indium, the conjugated polymer poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) is considered as one of the main substitutes for indium tin oxide (ITO) in the structure of organic photovoltaics. Recent works demonstrated that the blend of PEDOT:PSS and graphene oxide (GO) can provide transparent and flexible electrodes with a higher efficiency than PEDOT:PSS itself. In this study, two series of cooled and not-cooled thin films of GO:PEDOT:PSS with different compositions of PEDOT:PSS (1, 5, 10, and 100% (v/v)) were investigated by spectroscopic and morphological techniques to evaluate the effect of the cooling treatment on their electronic and chemical structures, morphology, and carrier mobility. Surface- and bulk-sensitive near-edge X-ray absorption fine structure (NEXAFS) results probed at the sulfur K-edge showed that the cooled GO:PEDOT:PSS 5% blend is the most organized film, which also presented a faster electron delocalization time as probed by resonant Auger spectroscopy using the core-hole clock method. GO:PEDOT:PSS 5% offers the best synergetic effect among the blends, a result which is completely in agreement with electrical results.</abstract><pub>American Chemical Society</pub><doi>10.1021/acs.jpcc.0c07827</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-4876-2464</orcidid><orcidid>https://orcid.org/0000-0001-6567-5920</orcidid><orcidid>https://orcid.org/0000-0001-5746-5632</orcidid><orcidid>https://orcid.org/0000-0002-3082-5869</orcidid><orcidid>https://orcid.org/0000-0002-0242-7820</orcidid><orcidid>https://orcid.org/0000-0002-2746-8565</orcidid><orcidid>https://orcid.org/0000-0002-1843-0741</orcidid></addata></record> |
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title | Conformational and Electron Dynamics Changes Induced by Cooling Treatment on GO:PEDOT:PSS Transparent Electrodes |
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