کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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5181911 | 1380974 | 2013 | 11 صفحه PDF | دانلود رایگان |

Poly(5-cyano indole) or PCIND and poly(3,4-ethylenedioxy pyrrole) or PEDOP films have been electro-synthesized for the first time in a hydrophobic ionic liquid: trihexyl(tetradecyl)phosphonium tris(pentafluoroethyl)trifluorophosphate. PCIND, is an anodically coloring electrochrome, and exhibited a reversible switching between a transmissive yellow and a saturated green hue, with an absorption maximum at 650Â nm in the fully oxidized state. Conducting atomic force microscopy studies revealed the PCIND film to be composed of an ensemble of segregated high current islands with a nanoscale electronic conductivity of 0.1Â SÂ cmâ1 and a band gap of 1.41Â eV. The cathodically coloring PEDOP film comprised of uniformly distributed and inter-connected high current carrying domains with a band gap of 1.82Â eV and a conductivity of 5.4Â SÂ cmâ1. Prototype electrochromic devices were fabricated using PEDOP and PCIND as cathode and anode with a thermally stable ionic liquid based, free standing polymeric gel film with a high ionic conductivity of 1.19Â ÃÂ 10â3Â SÂ cmâ1 as the electrolyte. The device showed large coloration efficiencies of 480 and 796Â cm2Â Câ1 at visible and NIR wavelengths of 475 and 1100Â nm respectively which far exceeded the coloration efficiencies of the individual electrochromes, thereby demonstrating the synergy between the two colorants. The performance attributes of the device, which switched reversibly between red, green and blue hues, are an outcome of an interplay between the high nanolevel electron conduction capabilities (enable fast charge transport) and high ion storage capacities (increase optical contrast as more number of electrochemically addressable sites are accessed by the electrolyte ions) of the PEDOP and PCIND films. Our studies demonstrate the applicability of PCIND films as anodic electrochromes in energy efficient windows.
Journal: Polymer - Volume 54, Issue 21, 4 October 2013, Pages 5801-5811