An ambipolar neutral state green polymeric electrochromic
Source abstract
Abstract
Abstract The synthesis and properties of highly stable neutral state green polymeric electrochromic, P1, which is based on 5,8-bis(2,3-dihydrothieno[3,4-b][1,4]dioxin-5-yl)-2,3-di(1H-pyrrol-2-yl)quinoxaline were highlighted. P1 exhibits three well-defined absorption bands with a narrow band gap (1.17 eV). The n- and p-doping (ambipolar) processes suggest that P1 is one of the most promising neutral state green polymers and it can be used in supercapacitors as either cathode or anode electrode material. Apart from the stability and the robustness of the polymer film, P1 shows multi-electrochromic behavior; gray-purple in the reduced form and highly transmissive blue color in the oxidized state.
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Research context
OpenAlex topics: Conducting polymers and applications · Transition Metal Oxide Nanomaterials · Organic Electronics and Photovoltaics
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (37)
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1. Buckley · J. Chem. Soc., Faraday Trans. 1 · 1975 · 71 · 144710.1039/f19757101447 ↗
2. Buckley · J. Chem. Soc., Faraday Trans. 1 · 1976 · 72 · 189610.1039/f19767201896 ↗
3. Burke · J. Electroanal. Chem. · 1980 · 107 · 20110.1016/S0022-0728(79)80021-2 ↗
4. Dautremont-Smith · Displays · 1982 · 3 · 310.1016/0141-9382(82)90061-0 ↗
5. Granqvist · Sol. Energy Mater. Sol. Cells · 2000 · 60 · 20110.1016/S0927-0248(99)00088-4 ↗
6. Granqvist · Thin Solid Films · 2003 · 442 · 20110.1016/S0040-6090(03)00983-0 ↗
7. Avendano · Thin Solid Films · 2006 · 496 · 3010.1016/j.tsf.2005.08.183 ↗
8. 2007
9. 2007
10. Schwendeman · Chem. Mater. · 2002 · 14 · 311810.1021/cm020050y ↗
11. Meng · Adv. Mater. · 2003 · 15 · 14610.1002/adma.200390030 ↗
12. Pennisi · Electrochim. Acta · 1999 · 44 · 323710.1016/S0013-4686(99)00042-0 ↗
13. Rauh · Electrochim. Acta · 1999 · 44 · 316510.1016/S0013-4686(99)00034-1 ↗
14. Mortimer · Chem. Soc. Rev. · 1997 · 26 · 14710.1039/cs9972600147 ↗
15. Rosseinsky · Adv. Mater. · 2001 · 13 · 78310.1002/1521-4095(200106)13:11<783::AID-ADMA783>3.0.CO;2-D ↗
16. Bange · Adv. Mater. · 1990 · 2 · 1010.1002/adma.19900020103 ↗
17. Burroughes · Nature · 1990 · 347 · 53910.1038/347539a0 ↗
18. Kraft · Angew. Chem. Int. Ed. · 1998 · 37 · 40210.1002/(SICI)1521-3773(19980302)37:4<402::AID-ANIE402>3.0.CO;2-9 ↗
19. Chandrasekhar · Adv. Funct. Mater. · 2002 · 12 · 9510.1002/1616-3028(20020201)12:2<95::AID-ADFM95>3.0.CO;2-N ↗
20. Forrest · Nature · 2004 · 428 · 91110.1038/nature02498 ↗
21. Reese · Mater. Today · 2004 · 7 · 2010.1016/S1369-7021(04)00398-0 ↗
22. Sotzing · Chem. Mater. · 1996 · 8 · 88210.1021/cm9504798 ↗
23. Groenendaal · Adv. Mater. · 2000 · 12 · 48110.1002/(SICI)1521-4095(200004)12:7<481::AID-ADMA481>3.0.CO;2-C ↗
24. Sonmez · Angew. Chem. Int. Ed. Engl. · 2004 · 43 · 149810.1002/anie.200352910 ↗
25. Sonmez · Macromolecules · 2005 · 38 · 66910.1021/ma0484173 ↗
26. Durmus · Chem. Commun. · 2007 · 324610.1039/b704936f ↗
27. Durmus · Chem. Mater. · 2007 · 19 · 624710.1021/cm702143c ↗
28. Durmus · Adv. Mater. · 2008 · 20 · 69110.1002/adma.200701979 ↗
29. Gunbas · Adv. Funct. Mater. · 2008 · 18 · 202610.1002/adfm.200701386 ↗
30. Beaujuge · Adv. Mater. · 2008 · 20 · 277210.1002/adma.200800280 ↗
31. Cihaner · Electrochim. Acta · 2008 · 53 · 257410.1016/j.electacta.2007.10.030 ↗
32. Cihaner · J. Electroanal. Chem. · 2008 · 614 · 10110.1016/j.jelechem.2007.11.024 ↗
33. Algı · Tetrahedron Lett. · 2008 · 49 · 353010.1016/j.tetlet.2008.03.139 ↗
34. Cihaner · Adv. Funct. Mater. · 2008 · 18 · 358310.1002/adfm.200801094 ↗
35. Aldakov · Chem. Commun. · 2003 · 139410.1039/b301362f ↗
36. Aldakov · J. Am. Chem. Soc. · 2004 · 126 · 475210.1021/ja039934o ↗
37. Anzenbacher · Tetrahedron · 2004 · 60 · 1116310.1016/j.tet.2004.08.060 ↗