High contrast ratio and fast-switching dual polymer electrochromic devices

被引:415
作者
Sapp, SA [1 ]
Sotzing, GA [1 ]
Reynolds, JR [1 ]
机构
[1] Univ Florida, Dept Chem, Ctr Macromol Sci & Engn, Gainesville, FL 32611 USA
关键词
D O I
10.1021/cm9801237
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A series of dual polymer electrochromic devices (ECDs) based on 12 complementary pairs of conducting polymer films have been constructed using 3,4-ethylenedioxythiophene-containing conducting polymers. Poly[3,6-bis(2-(3,4-ethylenedioxythiophene))-N-methylcarbazole] (PBEDOT-NCH(3)Cz), poly[3,6-bis(2-(3,4-ethylenedioxythiophene))-N-eicosylcarbazole] (PBEDOT-NC(20)H(41)Cz), and poly[4,4'-bis(2-(3, 4-ethylenedioxythiophene))biphenyl] (PBEDOTBP) were utilized as anodically coloring polymers that electrochemically switch between an oxidized deep blue absorptive state and a transmissive (orange or yellow) reduced state. Poly(3,4-ethylenedioxythiophene) (PEDOT) and its alkyl derivatives (PEDOT-C14H29 and PEDOT-C16H33) have been used as high-contrast cathodically coloring polymers that switch between a deep blue absorptive state in the reduced form and a sky blue, highly transmissive state in the oxidized form. The dual polymer ECDs were constructed by separating complementary pairs of EC polymer films, deposited on ITO glass, with a gel electrolyte composed of a lithium salt and plasticized poly(methyl methacrylate) (PMMA). Device contrast ratios, measured as Delta%T, ranged from 27% to 63%, and subsecond switching times for full color change were achieved. These devices were found to exhibit extremely high coloration efficiencies of up to 1400 cm(2)/C over narrow (ca. 100 nm) wavelength ranges and to retain up to 60% of their optical response after 10 000 deep, double potential steps, rendering them useful for EC applications.
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页码:2101 / 2108
页数:8
相关论文
共 66 条
[1]   ELECTROLUMINESCENCE FROM SUBSTITUTED POLY(THIOPHENES) - FROM BLUE TO NEAR-INFRARED [J].
ANDERSSON, MR ;
BERGGREN, M ;
INGANAS, O ;
GUSTAFSSON, G ;
GUSTAFSSONCARLBERG, JC ;
SELSE, D ;
HJERTBERG, T ;
WENNERSTROM, O .
MACROMOLECULES, 1995, 28 (22) :7525-7529
[2]   Poly(3-methylthiophenes) for an all polymer electrochromic device [J].
Arbizzani, C ;
Mastragostino, M ;
Meneghello, L ;
Morselli, M ;
Zanelli, A .
JOURNAL OF APPLIED ELECTROCHEMISTRY, 1996, 26 (01) :121-123
[3]   AN ELECTROCHROMIC WINDOW BASED ON A MODIFIED POLYPYRROLE NICKEL-OXIDE COMBINATION [J].
AVINO, C ;
PANERO, S ;
SCROSATI, B .
JOURNAL OF MATERIALS CHEMISTRY, 1993, 3 (12) :1259-1261
[4]  
Bange K., 1990, Advanced Materials, V2, P10, DOI 10.1002/adma.19900020103
[5]  
Bayer A. G, 1991, U. S. Patent, Patent No. [5 , 035, 926, 5035926]
[6]  
BYKER H, 1994, P ELECTROCHEM SOC, V94, P3
[7]  
CHUNG TC, 1984, PHYS REV B, V30, P702, DOI 10.1103/PhysRevB.30.702
[8]   FREE-ELECTRON ELECTROCHROMIC MODULATION IN CRYSTALLINE LIX WO3 [J].
COGAN, SF ;
PLANTE, TD ;
PARKER, MA ;
RAUH, RD .
JOURNAL OF APPLIED PHYSICS, 1986, 60 (08) :2735-2738
[9]   OPPORTUNITIES AND CHALLENGES OF ELECTROCHROMIC PHENOMENA IN TRANSITION-METAL OXIDES [J].
DEB, SK .
SOLAR ENERGY MATERIALS AND SOLAR CELLS, 1992, 25 (3-4) :327-338
[10]   ELECTROCHEMICAL AND SPECTROSCOPIC CHARACTERIZATION OF POLYALKYLENEDIOXYTHIOPHENES [J].
DIETRICH, M ;
HEINZE, J ;
HEYWANG, G ;
JONAS, F .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1994, 369 (1-2) :87-92