RESUMEN
The development of sustainable functional materials with strong potential to be applied in different areas has been growing and gaining increasing interest to address the environmental impact of current materials and technologies. In this scope, this work reports on sustainable functional materials with electrochromic properties, based on their increasing interest for a variety of applications, including sensing technologies. The materials have been developed based on a natural derived polymer, carrageenan, in which different amounts of the ionic liquid (IL) 1-ethyl-3-methylimidazolium thiocyanate ([EMIM][SCN]) were blended. It is shown that the addition of different amounts of IL to the carrageenan matrix does not affect the properties of the samples in terms of morphology or physicochemical and thermal properties, the most significant difference being the increase of the ionic conductivity with increasing IL content, ranging from 2.3 × 10-11 S·cm-1 for pristine carrageenan to 4.6 × 10-4 S·cm-1 for the samples with 5 and 60 wt % IL content, respectively. A electrochromic device has been developed based on the different IL/carrageenan samples as electrolyte and poly(3,4-ethylenedioxythiophene) polystyrenesulfonate (PEDOT:PSS) as electrodes. Spectroelectrochemistry testing demonstrates functional devices at low voltages between 0.3 and -0.9 V. Among the different samples, the one with 15 wt % IL content presents the best conditions for application, presenting an oxidation time of 6 s, a reduction time of 8 s, and a charge density of 1150 and 1050 µC·cm-2 for oxidation and reduction, respectively. The same sample also presents excellent optical density as a function of load density, presenting an optical switch (Δ%Tx) of 99%. Thus, it is demonstrated that it is possible to develop high efficiency and sustainable electrochromic devices based on natural polymers and ionic liquids.
RESUMEN
Solid polymer electrolytes (SPEs) are required to improve battery safety through the elimination of the liquid electrolyte solution in current batteries. This work is focused on the development of a hybrid SPE based on poly(vinylidene fluoride), PVDF, and 1-butyl-3-methylimidazolium cobalt(II) isothiocyanate, [BMIM]2[(SCN)4Co] magnetic ionic liquid (MIL), and its battery cycling behavior at room temperature. The addition of MIL in filler contents up to 40 wt % to the PVDF matrix does not influence the compact morphology of the samples obtained by solvent casting. The polar ß-phase of PVDF increases with increasing MIL content, whereas the degree of crystallinity, thermal degradation temperature, and mechanical properties of the MIL/PVDF blends decrease with increasing MIL content. The ionic conductivity of the MIL/PVDF blends increases both with temperature and MIL content, showing the highest ionic conductivity of 7 × 10-4 mS cm-1 at room temperature for the MIL/PVDF blend with 40 wt % of MIL. The cathodic half-cells prepared with this blend as SPE show good reversibility and excellent cycling behavior at different C-rates, with a discharge capacity of 80 mAh g-1 at a C/10-rate with a Coulombic efficiency of 99%. The developed magnetic SPE, with excellent performance at room temperature, shows potential for the implementation of sustainable lithium-ion batteries, which can be further tuned by the application of an external magnetic field.
