Nanostructured ultrathin films of alternating sexithiophenes and electropolymerizable polycarbazole precursor layers investigated by electrochemical surface plasmon resonance (EC-SPR) spectroscopy

Nanostructured ultrathin films of linear and dendrimeric cationic sexithiophenes, 6TNL and 6TND, respectively, alternated with anionic polycarbazole precursor, poly(2-( N-carbazolyl) ethyl methacrylate- co-methacrylic acid) or PCEMMA32, were successfully fabricated using the layer-by-layer self-asse...

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Veröffentlicht in:Langmuir : the ACS journal of surfaces and colloids. - 1992. - 24(2008), 16 vom: 19. Aug., Seite 9017-23
1. Verfasser: Sriwichai, Saengrawee (VerfasserIn)
Weitere Verfasser: Baba, Akira, Deng, Suxiang, Huang, Chengyu, Phanichphant, Sukon, Advincula, Rigoberto C
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2008
Zugriff auf das übergeordnete Werk:Langmuir : the ACS journal of surfaces and colloids
Schlagworte:Journal Article
Beschreibung
Zusammenfassung:Nanostructured ultrathin films of linear and dendrimeric cationic sexithiophenes, 6TNL and 6TND, respectively, alternated with anionic polycarbazole precursor, poly(2-( N-carbazolyl) ethyl methacrylate- co-methacrylic acid) or PCEMMA32, were successfully fabricated using the layer-by-layer self-assembly deposition technique. The two electro-optically active oligomers exhibited distinct optical properties and aggregation behavior in solution and films as studied by UV-vis and fluorescence spectroscopy. The stepwise increase of the 6TNL/PCEMMA32 and 6TND/PCEMMA32 layers was confirmed by UV-vis spectroscopy and in situ surface plasmon resonance (SPR) spectroscopy. The intralayer electrochemical polymerization and cross-linking behavior of the carbazole functionalized PCEMMA32 layers were then investigated using cyclic voltammetry (CV) and electrochemical surface plasmon resonance (EC-SPR) spectroscopy. The increase in current with each cycle confirmed intralayer cross-linking followed by the doping-dedoping process within these films. The two types of films differed with respect to dielectric constant and thickness changes before and after electropolymerization, indicating the influence of the oligothiophene layers. This demonstrated for the first time the preparation of highly ordered organic semiconductors alternated with in situ electropolymerizable layers in ultrathin films
Beschreibung:Date Completed 17.09.2008
Date Revised 13.08.2008
published: Print-Electronic
Citation Status PubMed-not-MEDLINE
ISSN:1520-5827
DOI:10.1021/la800307u