The formation of lipid bilayers between ionic liquid droplets is presented as a new means of forming functional
bimolecular networks. Ionic liquids are molten salts that have a number of interesting properties, such as the ability
to be a liquid at room temperature and exceedingly low vapor pressure. Our research demonstrates that it is possible
to consistently and repeatable form lipid bilayers on droplets of ionic liquid solutions. Characterization of the bilayers
interfaces shows that the ionic liquids have negligible effects on the stability and electrical properties of the bilayer. It
is also shown that the conductance levels in the gating events of Alamethicin peptide are affected by some ionic liquids.
Much attention has been given to ionic electroactive devices constructed using conducting polymers due to their low
voltage requirements, high strain, and similarities to natural muscle. However, the time response and output force of
conducting polymer actuators has always been a limiting factor in their implementation. In this study, we report on
a processing technique and parametric optimization for multilayer polypyrrole-gold-polyvinylidene fluoride (PPy-
Au-PVDF) composite actuators that have the possibility of overcoming the prior problems. These actuators are
operable in air, have faster time response, and are projected to generate higher force compared to that of
conventional conducting polymer actuators. These improvements are made possible due to the improvement in
processing conditions and novel multilayer geometry of the actuators. A five layer PPy-Au-PVDF-Au-PPy actuator
operating in air with 0.5M KCl electrolyte was shown to generate deflections up to 90% of the actuator length at a
rate of 50% per second.
Ionic polymer transducers (IPT) are a class of devices that leverage electroactive polymers (EAP), specifically
electrolyte-swollen ionomeric membranes, to perform energy conversions. Energy transformation from input to output is
referred to as transduction and occurs between the electrical and mechanical domains. The present study expands on IPT
investigations with a novel series of sulfonated polysulfones (sBPS), with specific interest in the effect of polymer
topology on actuator performance. A hydrophilic ionic liquid was combined with a series of sBPS through a casting
method to create hydrated membranes that contained target uptakes (f) of the diluent. The ionic liquid's hydrophilic, yet
organic nature raised the issue of its degree of compatibility and miscibility with the microphase separated domains of
the host ionomeric membrane. Initial studies of the ionomer - ionic liquid morphology were performed with synchrotron
small angle X-ray scattering (SAXS). The effective plasticization of the membranes was identified with dynamic
mechanical analysis (DMA) in terms of varied storage modulus and thermal transitions with ionic liquid uptake.
Electrical impedance spectroscopy (EIS) was employed to quantify the changes in ionic conductivity for each sBPS
ionomer across a range of uptake. Combined results from these techniques implied that the presence of large amounts of
ionic liquid swelled the hydrophilic domains of the ionomer and greatly increased the ionic conductivity. Decreases in
storage modulus and the glass transition temperature were proportional to one another but of a lesser magnitude than
changes in conductivity. The present range of ionic liquid uptake for sBPS was sufficient to identify the critical uptake
(fc) for three of the four ionomers in the series. Future work to construct IPTs with these components will use the critical
uptake as a minimum allowable content of ionic liquid to optimize the balance of electrical and mechanical properties
for the device components.
This study expands the number of novel synthetic ionomers specifically designed for performance as ionic polymer
transducers (IPT) membranes, specifically employing a highly branched sulfonated polysulfone. Control of the synthetic
design, characterization, and application of the novel ionomer is intended to allow fundamental study of the effect of
polymer branching on electromechanical transduction in IPTs. Fabrication methods were developed based upon the
direct application process (DAP) to construct a series of stand-alone electrodes as well as full IPTs with corresponding
electrode compositions. Specifically, the volumetric ratio of RuO2 conducting particles to the novel ionomeric matrix
was varied from 0 - 45 vol % in the electrodes. Electrical impedance spectroscopy was employed to determine the
electrical properties and their variation with electrode composition separate from and in the IPT. A percolation threshold
was detected for increased ionic conductivity of the stand-alone electrodes and the full IPTs based on increased loading
of conducting particles in the electrodes. An equivalent electrical circuit model was applied to fit the impedance data and
implicated interfacial and bulk effects contributing differently to the electrical properties of the electrodes and IPT as a
whole. The fabricated IPT series was further tested for bending actuation in response to applied step voltages and
represents the first demonstration of IPTs constructed with the DAP process using 100 % novel ionomer in all
components. The percolation behavior extended to the bending actuation responses for strain and voltage-normalized
strain rate and is useful in optimizing IPT components for maximum performance regardless of the ionomer employed.
Star-shaped polymers containing poly(isobutyl methacrylate) (iBMA) and poly(tert-butyl methacrylate) (t-BMA) arms coupled to a 2,5-dimethyl-2,5-hexanediol dimethacrylate (DHDMA) core were synthesized using arm-first living anionic polymerization. Gel permeation chromatography (GPC) indicated that coupling efficiencies were high and coupled products exhibited a monomodal molecular weight distribution. The star-shaped polymer number--average molecular weights were 8-10 times higher than the precursor arm molecular weights. The ratio of coupling reagent to living chain end concentration controlled the molecular weight of the star-shaped polymer and the number of coupled arms. The molecular weight distributions of the star-shaped polymers ranged from 1.5-2.0. Due to the labile tertiary- butyl esters contained in the DHDMA cores, these star-shaped polymers were readily hydrolyzed in the presence of acid catalysts. For example, poly(iBMA) star-shaped polymers were hydrolytically stable at 25 degree(s)C and hydrolyzed readily at 65 degree(s)C in the presence of hydrochloric acid. In addition, the poly(t-BMA) containing star--shaped polymers degraded under similar conditions. The degradation process for the iBMA and t-BMA containing star-shaped polymers was confirmed using 1H NMR spectroscopy, and poly(iBMA)-block- poly(methacrylic acid) and poly(methacrylic acid) were obtained, respectively.
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