posted on 2006-03-13, 11:11authored byRoger J. Mortimer, John R. Reynolds
An in situ colorimetric method, based on the CIE (Commission Internationale de l’Eclairage)
system of colorimetry, has been successfully applied to the study of electrochromism in
electrochemically deposited films of Prussian blue (iron(III) hexacyanoferrate(II), PB) on
transmissive ITO/glass substrates for the first time. On electrochemical reduction of PB to
Prussian white (iron(II) hexacyanoferrate(II), PW), sharp and reversible changes in the hue and
saturation occur, as shown by the track of the CIE 1931 xy chromaticity coordinates. For PB, the
CIELAB 1976 colour space coordinates were L* 5 73, a*5226 and b*5233, with a dominant
wavelength calculated as 488 nm. Concurrently, as the intensely absorbing PB mixed-valence
chromophore is ‘bleached’ to the transparent PW, a large increase in the relative luminance of the
electrochromic film is observed. On oxidation of PB, the CIELAB 1976 colour space coordinates
show the transition through intermediate green to the Prussian yellow (iron(III)
hexacyanoferrate(III), PY) state (L* 5 94, a* 5 2 and b* 5 18), with a steady increase in relative
luminance. To reliably compare the power requirement of PB films with other electrochromic
systems, composite coloration efficiencies (CCE’s) have been calculated, using a tandem
chronoabsorptometry/chronocoulometry method, as previously developed for organic polymer
systems. Using 95% of the total transmittance change at lmax as reference point, coloration
efficiencies, g 5 DA(lmax)/Q, were calculated as 143 and 150 cm2 C21 respectively for the PB/PW
and PW/PB electrochromic transitions.
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Citation
MORTIMER, R.J. and REYNOLDS, J.R., 2005. In situ colorimetric and composite coloration efficiency measurements for electrochromic Prussian blue. Journal of Materials Chemistry, 15, pp. 2226-2233.