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

Saengrawee Sriwichai, Akira Baba, Suxiang Deng, Chengyu Huang, Sukon Phanichphant, Rigoberto C. Advincula

Research output: Contribution to journalArticle

44 Citations (Scopus)

Abstract

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.

Original languageEnglish
Pages (from-to)9017-9023
Number of pages7
JournalLangmuir
Volume24
Issue number16
DOIs
Publication statusPublished - 2008 Aug 19
Externally publishedYes

Fingerprint

Ultrathin films
Surface plasmon resonance
surface plasmon resonance
Electropolymerization
Spectroscopy
Ultraviolet spectroscopy
spectroscopy
Semiconducting organic compounds
Methacrylates
Fluorescence spectroscopy
Oligomers
Self assembly
Cyclic voltammetry
Permittivity
Agglomeration
Optical properties
Doping (additives)
Acids
carbazoles
organic semiconductors

ASJC Scopus subject areas

  • Materials Science(all)
  • Condensed Matter Physics
  • Surfaces and Interfaces
  • Spectroscopy
  • Electrochemistry

Cite this

Nanostructured ultrathin films of alternating sexithiophenes and electropolymerizable polycarbazole precursor layers investigated by electrochemical surface plasmon resonance (EC-SPR) spectroscopy. / Sriwichai, Saengrawee; Baba, Akira; Deng, Suxiang; Huang, Chengyu; Phanichphant, Sukon; Advincula, Rigoberto C.

In: Langmuir, Vol. 24, No. 16, 19.08.2008, p. 9017-9023.

Research output: Contribution to journalArticle

Sriwichai, Saengrawee ; Baba, Akira ; Deng, Suxiang ; Huang, Chengyu ; Phanichphant, Sukon ; Advincula, Rigoberto C. / Nanostructured ultrathin films of alternating sexithiophenes and electropolymerizable polycarbazole precursor layers investigated by electrochemical surface plasmon resonance (EC-SPR) spectroscopy. In: Langmuir. 2008 ; Vol. 24, No. 16. pp. 9017-9023.
@article{7f23209f963c4495a6ba005d89b74d7b,
title = "Nanostructured ultrathin films of alternating sexithiophenes and electropolymerizable polycarbazole precursor layers investigated by electrochemical surface plasmon resonance (EC-SPR) spectroscopy",
abstract = "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.",
author = "Saengrawee Sriwichai and Akira Baba and Suxiang Deng and Chengyu Huang and Sukon Phanichphant and Advincula, {Rigoberto C.}",
year = "2008",
month = "8",
day = "19",
doi = "10.1021/la800307u",
language = "English",
volume = "24",
pages = "9017--9023",
journal = "Langmuir",
issn = "0743-7463",
publisher = "American Chemical Society",
number = "16",

}

TY - JOUR

T1 - Nanostructured ultrathin films of alternating sexithiophenes and electropolymerizable polycarbazole precursor layers investigated by electrochemical surface plasmon resonance (EC-SPR) spectroscopy

AU - Sriwichai, Saengrawee

AU - Baba, Akira

AU - Deng, Suxiang

AU - Huang, Chengyu

AU - Phanichphant, Sukon

AU - Advincula, Rigoberto C.

PY - 2008/8/19

Y1 - 2008/8/19

N2 - 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.

AB - 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.

UR - http://www.scopus.com/inward/record.url?scp=50849112706&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=50849112706&partnerID=8YFLogxK

U2 - 10.1021/la800307u

DO - 10.1021/la800307u

M3 - Article

C2 - 18616227

AN - SCOPUS:50849112706

VL - 24

SP - 9017

EP - 9023

JO - Langmuir

JF - Langmuir

SN - 0743-7463

IS - 16

ER -