Electrochromic devices and thin film transistors from a new family of ethylenedioxythiophene based conjugated polymers

被引:26
作者
Li, Zhongtao [1 ]
Zhang, Yuan [3 ]
Holt, Amanda L. [1 ]
Kolasa, Borys P. [2 ]
Wehner, Justin G. [2 ]
Hampp, Andreas [2 ]
Bazan, Guillermo C. [3 ]
Thuc-Quyen Nguyen [3 ]
Morse, Daniel E. [1 ]
机构
[1] Univ Calif Santa Barbara, Inst Collaborat Biotechnol, Santa Barbara, CA 93106 USA
[2] Raytheon Vis Syst, Goleta, CA 93117 USA
[3] Univ Calif Santa Barbara, Dept Chem & Biochem, Inst Polymers & Organ Solids, Santa Barbara, CA 93106 USA
关键词
CHARGE-TRANSFER; INFRARED ELECTROCHROMISM; BULK-HETEROJUNCTIONS; COPOLYMERS; ELECTROCHEMISTRY; DERIVATIVES; SYSTEMS; CELLS;
D O I
10.1039/c0nj00837k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
New electrochromic conjugated polymers and their corresponding devices based on EDOT (ethylenedioxythiophene) are described. The best of these polymers display response times on the order of 1s and high switchable contrast in the visible and near-infrared (Vis-NIR) spectral regions. Thin films (70 nm) of these new polymers displayed optical band gaps on the order of 1.73 eV (7a) < 2.19 eV (7b) < 2.23 eV (7c) < 2.31 eV (4) < 2.34 eV (2) as calculated from their extrapolation of the absorption edges. Polymers 4 and 7a show field effect hole mobilities of ca. 6.7 x 10(-5) cm(2) V(-1) s(-1) (on/off ratio 10(4)) and 2.5 x 10(-5) cm(2) V(-1) s(-1) (on/off ratio 10(3)), respectively, related to their highly ordered inter-chain packing as confirmed by XRD analyses of polymer 4. Electrochromic characterizations show that polymers 7a-c exhibit significant absorption changes in the infrared at low voltage. The resulting solid-state devices offer promise for electrochromic shutters and filters in the IR, since their high charge transfer mobility and ion injection efficiency permits relatively rapid switching and good switchable contrast, while their robustness exceeds that of aqueous devices.
引用
收藏
页码:1327 / 1334
页数:8
相关论文
共 37 条
[1]   The first truly all-polymer electrochromic devices [J].
Argun, AA ;
Cirpan, A ;
Reynolds, JR .
ADVANCED MATERIALS, 2003, 15 (16) :1338-+
[2]  
ARGUN AA, 2003, ADV MATER, P15
[3]   Color Control in π-Conjugated Organic Polymers for Use in Electrochromic Devices [J].
Beaujuge, Pierre M. ;
Reynolds, John R. .
CHEMICAL REVIEWS, 2010, 110 (01) :268-320
[4]   Toward a rational design of poly(2,7-carbazole) derivatives for solar cells [J].
Blouin, Nicolas ;
Michaud, Alexandre ;
Gendron, David ;
Wakim, Salem ;
Blair, Emily ;
Neagu-Plesu, Rodica ;
Belletete, Michel ;
Durocher, Gilles ;
Tao, Ye ;
Leclerc, Mario .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2008, 130 (02) :732-742
[5]   Far infrared electrochromism in unique conducting polymer systems [J].
Chandrasekhar, P ;
Birur, GC ;
Stevens, P ;
Rawal, S ;
Pierson, EA ;
Miller, KL .
SYNTHETIC METALS, 2001, 119 (1-3) :293-294
[6]  
CHANDRASEKHAR P, 1999, Patent No. 5995273
[7]  
Deb S K, 1969, Appl Opt, V8 Suppl 1, P192
[8]   OPTICAL AND PHOTOELECTRIC PROPERTIES AND COLOR CENTERS IN THIN-FILMS OF TUNGSTEN OXIDE [J].
DEB, SK .
PHILOSOPHICAL MAGAZINE, 1973, 27 (04) :801-822
[9]  
F Armarego W.L., 2013, Purification of Laboratory Chemicals, VSeventh
[10]   Electrochemistry of poly(3,4-alkylenedioxythiophene) derivatives [J].
Groenendaal, L ;
Zotti, G ;
Aubert, PH ;
Waybright, SM ;
Reynolds, JR .
ADVANCED MATERIALS, 2003, 15 (11) :855-879