An in situ colorimetric measurement study of electrochromism in the di-n-heptyl viologen system

被引:40
作者
Mortimer, Roger J. [1 ,2 ]
Reynolds, John R. [2 ]
机构
[1] Univ Loughborough, Dept Chem, Loughborough LE11 3TU, Leics, England
[2] Univ Florida, Ctr Macromol Sci & Engn, Dept Chem, George & Josephine Butler Polymer Res Lab, Gainesville, FL 32611 USA
基金
英国工程与自然科学研究理事会;
关键词
Electrochromic; Electrochromism; CIE colour coordinates; Colorimetry; N ',N '-Bis(n-heptyl)-4,4 '-bipyridylium; Di-n-heptyl viologen;
D O I
10.1016/j.displa.2008.02.002
中图分类号
TP3 [计算技术、计算机技术];
学科分类号
0812 ;
摘要
An in situ colorimetric method, based on the CIE (Commission Internationale de l'Eclairage) system of colorimetry, has been applied to the study of the electrochromic N,N'-bis(n-heptyl)-4,4'-bipyridylium (di-n-heptyl viologen) system in aqueous solution on transmissive ITO/glass Substrates. on electrochemical reduction of the di-n-heptyl viologen di-cation, the purple di-n-heptyl viologen radical cation salt deposits as a film and the changes in hue and saturation have been tracked using CIE 1911 xy chromaticity coordinates. The CIE-LAB 1976 colour space coordinates of the purple di-n-heptyl viologen radical cation salt were L* = 76, a* = 33, and b* = -20, with a complementary wavelength of 548 nm. A sharp decrease in luminance Was found on formation of the di-n-heptyl viologen radical cation salt. Colour coordinates for the reverse (oxidation) direction plots show hysteresis, implying that specific choice of colour values depends oil both the potential applied and from which direction the potential is changed. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:424 / 431
页数:8
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