Layer-by-layer assembly of poly(aniline-N-butylsulfonate)s and their electrochromic properties in an all solid state window

被引:17
作者
Jung, SY [1 ]
Kim, HJ [1 ]
Han, MJ [1 ]
Kang, YK [1 ]
Kim, EY [1 ]
机构
[1] Korea Res Inst Chem Technol, Adv Mat Div, Taejon 305600, South Korea
来源
MATERIALS SCIENCE & ENGINEERING C-BIOMIMETIC AND SUPRAMOLECULAR SYSTEMS | 2004年 / 24卷 / 1-2期
关键词
LBL self-assembly; poly(aniline-N-butylsulfonate); electrochromic;
D O I
10.1016/j.msec.2003.09.052
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Layer-by-layer (LBL) self-assembly by sequential adsorption of a polyanion, poly(aniline-N-butylsulfonate)s (PANBUS), onto oppositely charged cation, vinylbenzyldimethyldodecylammonium chloride (VDAC), led to the formation of ultra thin films at indium-tin oxide (ITO) glasses. The building up of such multilayer films was characterized by the increment of the absorbance through UV-visible spectroscopy, which indicated a linear dependence of the absorbance on the number of deposition cycles from 1 to 11 bilayers. Atomic force microscopy (AFM) showed that the size of PANBUS platelets increases with the number of bilayers, to result in clumps of PANBUS bundles in the 11-bilayer PANBUS films. Electrochromic (EC) properties of the PANBUS film coated on an ITO glass in contact to an ion conducting polymer film were investigated. The ion conducting polymer films were prepared via photocross-linking reactions of methoxy poly(ethylene glycol) monomethacrylate with trially-1,3,5-triazine-2,4,6-(1H,3H,5H)-trione in the presence of LiCF3SO3 and a photoinitiator. In situ spectroelectrochemical study showed reversible electrochromic response with optical contrast higher than 0.1 and response times of similar to 10 s when the number of bilayers was less than 10. EC property in thicker PANBUS films, showing slower response, was related to the topological change in the LBL film. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:57 / 60
页数:4
相关论文
共 11 条
[1]   Molecular-level processing of conjugated polymers .3. Layer-by-layer manipulation of polyaniline via electrostatic interactions [J].
Cheung, JH ;
Stockton, WB ;
Rubner, MF .
MACROMOLECULES, 1997, 30 (09) :2712-2716
[2]   Fuzzy nanoassemblies: Toward layered polymeric multicomposites [J].
Decher, G .
SCIENCE, 1997, 277 (5330) :1232-1237
[3]   Polymer-clay nanocomposites: exfoliation of organophilic montmorillonite nanolayers in polystyrene [J].
Fu, X ;
Qutubuddin, S .
POLYMER, 2001, 42 (02) :807-813
[4]   Brewster Angle Microscope and Atomic Force Microscopy study of poly 4-(n-methacyloyl)-Disperse Red 1-methacrylic acid monolayer at the air/water interface and on the glass surface [J].
Kang, YS ;
An, SD .
MOLECULAR CRYSTALS AND LIQUID CRYSTALS, 2001, 371 :53-56
[5]   LIQUID-CRYSTALLINE ASSEMBLIES FROM SELF-DOPED POLYANILINES [J].
KIM, E ;
LEE, M ;
LEE, MH ;
RHEE, SB .
SYNTHETIC METALS, 1995, 69 (1-3) :101-104
[6]   All solid-state electrochromic window based on poly(aniline N-butylsulfonate)s [J].
Kim, E ;
Lee, KY ;
Lee, MH ;
Shin, JS ;
Rhee, SB .
SYNTHETIC METALS, 1997, 85 (1-3) :1367-1368
[7]   Electrochromic window based on poly(aniline-N-butylsulfonate)s with a radiation-cured solid polymer electrolyte film [J].
Kim, E ;
Lee, K ;
Rhee, SB .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1997, 144 (01) :227-232
[8]   REDOX CYCLABILITY OF A SELF-DOPED POLYANILINE [J].
KIM, EY ;
LEE, MH ;
MOON, BS ;
LEE, CJ ;
RHEE, SB .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1994, 141 (03) :L26-L28
[9]   Scanning force microscope studies of Langmuir-Blodgett polyaniline thin films [J].
Porter, TL ;
Thompson, D ;
Bradley, M .
THIN SOLID FILMS, 1996, 288 (1-2) :268-271
[10]   Physical properties of polyaniline films: Assembled by the layer-by-layer technique [J].
Ram, MK ;
Salerno, M ;
Adami, M ;
Faraci, P ;
Nicolini, C .
LANGMUIR, 1999, 15 (04) :1252-1259