Orange and Red to Transmissive Electrochromic Polymers Based on Electron-Rich Dioxythiophenes

被引:143
作者
Dyer, Aubrey L. [1 ]
Craig, Michael R. [1 ,2 ]
Babiarz, Joseph E. [2 ]
Kiyak, Kelly [2 ]
Reynolds, John R. [1 ]
机构
[1] Univ Florida, George & Josephine Butler Polymer Labs, Dept Chem, Ctr Macromol Sci & Engn, Gainesville, FL 32611 USA
[2] BASF, Tarrytown, NY 10591 USA
关键词
PROCESSABLE GREEN; DEVICES;
D O I
10.1021/ma100366y
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
As the color palette of available solution processable electrochromic polymers expands, there has remained the need for red, orange, and yellow to transmissive switching materials. Here we report on the synthesis and characterization of two such polymers, the orange to transmissive switching (poly{3,4-di(2-ethylhexyloxy)thiophene}) electrochromic polymer-orange (ECP-orange) and the red to transmissive switching processable polymer (poly{3,4-di(2-ethylhexyloxy)thiophene-co-3,4-di(methoxy)thiophene}) electrochromic polymer-red (ECP-red). The ECP-orange has a bandgap of 2.04 eV, an absorption lambda(max) centered at 483 nm, and an E-1/2 of 0.37 V versus Ag/Ag+. The electrochromic contrast is 48% T at 483 nm with a time to reach 95% of the full optical contrast of 5.3 s for a film that has an absorbance of 0.98 au at lambda(max). Because of steric relaxations from the random copolymerization of a branched dialkoxy-substituted thiophene with a dimethoxy-substituted thiophene, the red to transmissive switching ECP-red has a bandgap of 2.00 eV, a lambda(max) red-shifted by 42 to 525 nm, and an E-1/2 decreased to 0.21 V versus Ag/Ag+ Additionally, the red polymer has a higher contrast of 60% T and a shorter time to reach 95% of the full optical contrast of 2.3 s. These two reported polymers allow the field of electrochromics to come closer to a full set of fully solution processable materials that yield films whose optical absorption covers the full visible spectrum while switching to a highly transmissive oxidized state as needed for full color displays.
引用
收藏
页码:4460 / 4467
页数:8
相关论文
共 50 条
[1]   Spray-Processable Blue-to-Highly Transmissive Switching Polymer Electrochromes via the Donor-Acceptor Approach [J].
Amb, Chad M. ;
Beaujuge, Pierre M. ;
Reynolds, John R. .
ADVANCED MATERIALS, 2010, 22 (06) :724-+
[2]   Printable all-organic electrochromic active-matrix displays [J].
Andersson, Peter ;
Forchheimer, Robert ;
Tehrani, Payman ;
Berggren, Magnus .
ADVANCED FUNCTIONAL MATERIALS, 2007, 17 (16) :3074-3082
[3]  
[Anonymous], 1986, CIE 15.2: Colorimetry
[4]   Properties, requirements and possibilities of smart windows for dynamic daylight and solar energy control in buildings: A state-of-the-art review [J].
Baetens, Ruben ;
Jelle, Bjorn Petter ;
Gustavsen, Arild .
SOLAR ENERGY MATERIALS AND SOLAR CELLS, 2010, 94 (02) :87-105
[5]   The donor-acceptor approach allows a black-to-transmissive switching polymeric electrochrome [J].
Beaujuge, P. M. ;
Ellinger, S. ;
Reynolds, J. R. .
NATURE MATERIALS, 2008, 7 (10) :795-799
[6]   Spray processable green to highly transmissive electrochromics via chemically polymerizable donor-acceptor heterocyclic pentamers [J].
Beaujuge, Pierre M. ;
Ellinger, Stefan ;
Reynolds, John R. .
ADVANCED MATERIALS, 2008, 20 (14) :2772-+
[7]   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
[8]   Unsaturated Linkages in Dioxythiophene-Benzothiadiazole Donor-Acceptor Electrochromic Polymers: The Key Role of Conformational Freedom [J].
Beaujuge, Pierre M. ;
Vasilyeva, Svetlana V. ;
Ellinger, Stefan ;
McCarley, Tracy D. ;
Reynolds, John R. .
MACROMOLECULES, 2009, 42 (11) :3694-3706
[9]   Multicolored Electrochromic Cells Based On Poly(2,7-Carbazole) Derivatives For Adaptive Camouflage [J].
Beaupre, Serge ;
Breton, Anne-Catherine ;
Dumas, Jean ;
Leclerc, Mario .
CHEMISTRY OF MATERIALS, 2009, 21 (08) :1504-1513
[10]   Photophysics and electrochemistry of conjugated oligothiophenes prepared by using azomethine connections [J].
Bourgeaux, Marie ;
Skene, W. G. .
JOURNAL OF ORGANIC CHEMISTRY, 2007, 72 (23) :8882-8892