Electrochromic
materials (ECMs) change their colored state with
changes in potential. When applied as an energy storage device, they
reveal the current state of charge using intrinsic properties already
within the ECM. This is possible because supercapacitors of the faradaic
type, called pseudocapacitors, rely on the same redox reactions that
induce the color change in ECMs. In this work, molecularly defined
metal complexes were covalently attached to a surface-enhanced indium
tin oxide nanoparticle-based screen-printed support to form a monolayer.
We have investigated these monolayers for their ability to store and
release a charge while retaining their electrochromic properties.
Iron(II), cobalt(II), and osmium(II) complexes were deposited separately
or simultaneously leading to corresponding single- or triple-metal
materials. Spectroscopic and galvanostatic charge–discharge
measurements confirm the dual electrochromic and energy storage nature
of the devices in a range of currents. The introduction of a transparent
charge storing TiO2 layer at the counter electrode improves
the current density, capacitance, response time, and long-term performance
of the triple-metal electrochromic device. This work adds to a limited
number of chromophoric metal coordination complexes applied within
energy storage devices.