journal article·2009-06-23

Tuning the Electrochromic Properties of Poly(alkyl-3,4-ethylenedioxyselenophenes) Having High Contrast Ratio and Coloration Efficiency

Mao Li, Yana Sheynin, Asit Patra, Michael Bendikov

Chemistry of Materials· Volume 21· Issue 12
Publisher page

Abstract

A systematic study of the electrochemical, spectroelectrochemical and electrochromic (EC) properties of poly(alkyl-3,4-ethylenedioxyselenophene) (PEDOS-C n ) ( n = 0, 2, 4, 6, 8 and 12) films is reported. The alkyl substituents lead PEDOS-C n films to exhibit sharper redox peaks than the parent PEDOS film and raise an onset of their oxidation potentials by 0.20−0.62 V. As expected, the introduction of alkyl chains significantly improves the EC properties and the electrochemical stability of PEDOS-C n films and results in high contrast ratios and coloration efficiencies, low switching voltages, and fast switching times. As the length of the alkyl chain increases, the broad absorption peak of PEDOS sharpens and splits into three distinct peaks for PEDOS-C n films starting from n = 4. We have identified the correlations between EC properties (such as coloration efficiency) and other observed properties of PEDOS-C n films (such as their peak width, the position of the maximum absorption peak, the ratio of the absorption intensity of NIR spectra peaks to visible spectra peaks) and the contrast ratio. Interestingly, EC properties show bell-shaped behavior as a function of alkyl chain length, which reaches the maximum for PEDOS-C 6 film, whereas the EC properties of films with shorter and longer alkyl chains are poorer.
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Research context

OpenAlex topics: Conducting polymers and applications · Transition Metal Oxide Nanomaterials · Advanced Sensor and Energy Harvesting Materials

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Affiliations

Department of Organic Chemistry, Weizmann Institute of Science, Rehovot, 76100 Israel

References (43)

Show source-provided references
1. Monk P. M. S. · 200710.1017/CBO9780511550959 ↗
2. Dyer A. L. · 2007
3. Mortimer R. J. · Chem. Soc. Rev. · 1997 · 26 · 14710.1039/cs9972600147 ↗
4. Rosseinsky D. R. · Adv. Mater. · 2001 · 13 · 78310.1002/1521-4095(200106)13:11<783::AID-ADMA783>3.0.CO;2-D ↗
5. Bange K. · Adv. Mater. · 1990 · 2 · 1010.1002/adma.19900020103 ↗
6. Chandrasekhar P. · Adv. Funct. Mater. · 2002 · 12 · 9510.1002/1616-3028(20020201)12:2<95::AID-ADFM95>3.0.CO;2-N ↗
7. Motiei L. · J. Am. Chem. Soc. · 2009 · 131 · 346810.1021/ja900507c ↗
8. Arbizzani C. · Adv. Mater. · 1995 · 7 · 57110.1002/adma.19950070614 ↗
9. Tovar J. D. · Adv. Mater. · 2001 · 13 · 177510.1002/1521-4095(200112)13:23<1775::AID-ADMA1775>3.0.CO;2-N ↗
10. Walczak R. M. · Macromolecules · 2008 · 41 · 69110.1021/ma071589q ↗
11. Schottland P. · Macromolecules · 2000 · 33 · 705110.1021/ma000490f ↗
12. Verghese M. M. · Adv. Mater. Opt. Electron. · 1996 · 6 · 39910.1002/(SICI)1099-0712(199609)6:5/6<399::AID-AMO290>3.0.CO;2-F ↗
13. Verghese M. M. · Polymer · 1997 · 38 · 162510.1016/S0032-3861(96)00655-6 ↗
14. Zotti G. · Adv. Mater. · 1992 · 4 · 74910.1002/adma.19920041110 ↗
15. Heywang G. · Adv. Mater. · 1992 · 4 · 11610.1002/adma.19920040213 ↗
16. Groenendaal L. · Adv. Mater. · 2000 · 12 · 48110.1002/(SICI)1521-4095(200004)12:7<481::AID-ADMA481>3.0.CO;2-C ↗
17. Sankaran B. · Macromolecules · 1997 · 30 · 258210.1021/ma961607w ↗
18. Gaupp G. L. · Chem. Mater. · 2002 · 14 · 396410.1021/cm020433w ↗
19. Schwendeman I. · Adv. Funct. Mater. · 2003 · 13 · 54110.1002/adfm.200304372 ↗
20. Welsh D. M. · Adv. Mater. · 1999 · 11 · 137910.1002/(SICI)1521-4095(199911)11:16<1379::AID-ADMA1379>3.0.CO;2-Q ↗
21. Welsh D. M. · Macromolecules · 2002 · 35 · 651710.1021/ma0120409 ↗
22. Gaupp C. L. · Macromol. Rapid Commun. · 2002 · 23 · 88510.1002/1521-3927(20021001)23:15<885::AID-MARC885>3.0.CO;2-X ↗
23. Sotzing G. A. · Adv. Mater. · 1997 · 9 · 79510.1002/adma.19970091005 ↗
24. Heuer H. W. · Adv. Funct. Mater. · 2002 · 12 · 8910.1002/1616-3028(20020201)12:2<89::AID-ADFM89>3.0.CO;2-1 ↗
25. Wang C. · Chem. Mater. · 1995 · 7 · 5810.1021/cm00049a011 ↗
26. Reeves B. D. · Adv. Mater. · 2002 · 14 · 71710.1002/1521-4095(20020517)14:10<717::AID-ADMA717>3.0.CO;2-D ↗
27. Reeves B. D. · Macromolecules · 2004 · 37 · 755910.1021/ma049222y ↗
28. Krishnamoorthy K. · J. Mater. Chem. · 2001 · 11 · 290910.1039/b108654e ↗
29. Sonmez G. · Adv. Funct. Mater. · 2003 · 13 · 72610.1002/adfm.200304317 ↗
30. Sonmez G. · Chem. Mater. · 2004 · 16 · 57410.1021/cm0301773 ↗
31. Patra A. · J. Am. Chem. Soc. · 2008 · 130 · 673410.1021/ja8018675 ↗
32. Li M. · Adv. Mater. · 2009 · 21 · 170710.1002/adma.200802259 ↗
33. Havinga E. E. · Chem. Mater. · 1996 · 8 · 76910.1021/cm9504551 ↗
34. Yalcinkaya F. · Med. Eng. Phys. · 1997 · 19 · 29910.1016/S1350-4533(96)00034-3 ↗
35. Coloration efficiency, in units of cm2/C at a specified wavelength, can be expressed as CE(λ) = ΔOD/Qd. The values of these terms are obtained by determining the injected/ejected charge as a function of the electrode area (expressed in terms of charge density (Qd) in units of C/cm2) and by determining the change in optical density (ΔOD) (which is obtained from the chromoabsorptometry and chronocoulometry data acquired from the redox step of the polymer). ΔOD at a specified wavelength is expressed as △OD = log[Tb(λ)/Tc(λ)], whereTbandTcare the transmittance in the bleached and colored states, respectively. See refs1a,1e, and9.
36. The redox potential of PEDOT film is−0.39 V under the same conditions.
37. Schwendeman I. · Adv. Mater. · 2001 · 13 · 63410.1002/1521-4095(200105)13:9<634::AID-ADMA634>3.0.CO;2-3 ↗
38. Strong broad absorption around 1400−1500 cm−1was observed in Raman spectra of PEDOS.Hernández, V.; Bendikov, M.To be published.
39. Apperloo J. J. · Chem.—Eur. J. · 2002 · 8 · 238410.1002/1521-3765(20020517)8:10<2384::AID-CHEM2384>3.0.CO;2-L ↗
40. Turbiez M. · Chem.—Eur. J. · 2005 · 11 · 374210.1002/chem.200401058 ↗
41. Turbiez M. · J. Org. Chem. · 2003 · 68 · 535710.1021/jo0345493 ↗
42. For the photo of PEDOS-C6film, see ref16.
43. Groenendaal L. · Synth. Met. · 2001 · 118 · 10510.1016/S0379-6779(00)00289-7 ↗