In situ spectroelectrochemistry and colour measurement of a complementary electrochromic device based on surface-confined Prussian blue and aqueous solution-phase methyl viologen

• Published in: Solar energy materials and solar cells Vol. 99; pp. 213 - 220
• Main Authors: Mortimer, Roger J., Varley, Thomas S.
• Format: Journal Article
• Language: English
• Published: Amsterdam Elsevier B.V 01-04-2012; Elsevier
• Subjects: Applied sciences; Bleaching; CIE chromaticity coordinates; Color; Color measurement; Colorimetry; Colour; Devices; Electrochromic; Electrochromism; Energy; Exact sciences and technology; Methyl viologen; Miscellaneous; Natural energy; Prussian blue; Solar energy; Spectra; Switching; CIE chromaticity coordinates; Electrochromism; Prussian blue; Colorimetry; Electrochromic; Methyl viologen; Hexacyanoferrates; Initial condition; Cathode; In situ; Iron; Electrochromic device; Switching; Color space; Chromaticity; Oxidation; Aqueous solution; Mixed valence; Transparent material; Spectroelectrochemistry; Chromophore
• ISSN: 0927-0248; 1879-3398
• DOI: 10.1016/j.solmat.2011.11.052

The fabrication, in situ spectroelectrochemistry and colour measurement of hybrid electrochromic devices (ECDs) based on a surface-confined metal hexacyanometallate – Prussian blue (PB, containing the iron(III) hexacyanoferrate(II) chromophore) – and aqueous solution-phase methyl viologen (N,N′-dimethyl-4,4′-bipyridylium) are described. In the ECDs, the initial (‘off’) bleached state is set with PB in its reduced form and the methyl viologen as the di-cation. Switching to the coloured state (‘on’), forms the mixed-valence iron(III) hexacyanoferrate(II) chromophore upon oxidation of iron(II) hexacyanoferrate(II), with simultaneous reduction of the methyl viologen di-cation to form a mixture of the radical cation monomer/dimer. Using the Commission Internationale de l'Eclairage (CIE) system of colorimetry, the colour stimulus of such ECDs and the changes that take place on reversibly switching between the colourless and coloured states have been calculated from in situ visible region spectra recorded under electrochemical control. The concentration of the solution-phase methyl viologen and its diffusion to the cathode controlled both the proportion of surface-confined (reduced) PB that is switched to the blue form and the overall ECD changes. For the ECDs' ‘on’ states, the CIELAB 1976 colour space coordinates for a D55 illuminant were L⁎=60, a⁎=3 and b⁎=−46, and L⁎=49, a⁎=9 and b⁎=−59, respectively for 5 and 10mM methyl viologen solution concentrations. The low a⁎ and high (negative) b⁎ chromaticity coordinates quantified the overall ECD colour stimulus of the ‘on’ state as being deep blue, with a broad absorption across the visible spectral region. CIELAB 1976 colour space coordinates showed that the ECDs were fully transparent and nearly colourless in the ‘off’ states, with L⁎=100, a⁎=1 and b⁎=1. The changes in the transparency were 83.0% (5mM methyl viologen) and 93.1% (10mM methyl viologen) between the ‘off’ (bleached) and ‘on’ (coloured) states of the ECDs.
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► A Prussian blue/methyl viologen electrochromic device is described. ► In situ spectra during colour switching are measured. ► Colour stimuli are quantified using CIE principles. ► The device exhibits near colourless and deep blue colour states.