Graphene-Enhanced Ion Transport in Dual-Conducting Composite Films of Polyacetylene and an Imidazolium Iodide Ionic Liquid.

Dual-conducting polymer films were synthesized by dispersing graphene in an aqueous solution of poly(vinyl alcohol) and 1-propyl-3-methylimidazolium iodide ([C3mim]I) ionic liquid and thermally converting the poly(vinyl alcohol) to polyene in the presence of hydroiodic acid catalyst. The electrical and mechanical properties of the resulting free-standing films of the nanocomposite, containing different concentrations of graphene, were analyzed using electrochemical impedance spectroscopy (EIS) and dynamic mechanical analysis (DMA), respectively. Nyquist plots (imaginary vs real components of the frequency-dependent impedance) showed two characteristic arcs representing the composite's electronic and ionic conduction pathways. The conductivity values corresponding to both charge transport mechanisms increased with temperature and the graphene concentration. The enhancement in electronic conductivity is expected because of graphene's high electron mobility. Interestingly, ionic conductivity also showed a significant increase with graphene concentration, approximately triple the extent of the rise in the electronic conductivity, even though the loss and storage moduli of the films increased. (Generally, a higher modulus results in lower ionic conductivities in ionic gels.) Molecular dynamics simulations of the three-component system provided some insights into this unusual behavior. Mean square displacement data showed that the diffusion of the iodide anions was relatively isotropic. The iodide diffusion coefficient was higher in a blend with 5 vol % graphene than in blends with 3 vol % graphene or no graphene. The improvement is attributed to the interfacial effects of the graphene on the free volume of the blend. Furthermore, an exclusion of the iodide ions from the vicinity of graphene was observed in the radial distribution function analysis. The increase in the effective concentration of iodide due to this exclusion and the increase in its diffusion coefficient because of the excess free volume are the primary reasons for the observed enhancement in ionic conductivity by adding graphene.

Asymmetric and Symmetric Redox Flow Batteries for Energy-Efficient, High-Recovery Water Desalination.

Electrochemical separation offers an energy-efficient means to desalinate brackish water, a relatively untapped but increasingly utilized water source for freshwater supply. Several electrochemical techniques are being developed to enable low-energy desalination combined with energy storage. We report a new approach that produced a peak power density of 6.0 mW cm-2 from the energy stored in iron cyanide (Fe-CN) and iron citrate (Fe-Cit) redox couples during water desalination, using asymmetric redox flow batteries (RFBs). Desalination and the charging of the redox couples occurred in a four-channel RFB cell. The stored energy was extracted in a two-channel RFB cell. Desalination of model brackish water (2.9 g L-1) to freshwater (0.5 g L-1) was also studied in a symmetric system using the environmentally benign Fe-Cit. The process was characterized by low energy consumption (0.56 kW h m-3), high productivity (41.1 L freshwater m-2 area h-1, representing practical operating conditions for brackish water desalination), and high water recovery (91% product-to-intake water ratio, addressing the environmental and economic challenges of brine disposal). The low cell voltage (<0.5 V) required in the reported system is ideally suited for developing modular desalination systems powered by renewables, including solar energy. Collectively, water-based RFBs for desalination and power production would lead to sustainable water-energy infrastructure.

Interfacial characteristics of a PEGylated imidazolium bistriflamide ionic liquid electrolyte at a lithium ion battery cathode of LiMn2O4.

Nonvolatile and nonflammable ionic liquids (ILs) have distinct thermal advantages over the traditional organic solvent electrolytes of lithium ion batteries. However, this beneficial feature of ILs is often counterbalanced by their high viscosity (a limiting factor for ionic conductivity) and, sometimes, by their unsuitable electrochemistry for generating protective layers on electrode surfaces. In an effort to alleviate these limiting aspects of ILs, we have synthesized a PEGylated imidazolium bis(trifluoromethylsulfonyl)amide (bistriflamide) IL that exhibited better thermal and electrochemical stability than a conventional electrolyte based on a blend of ethylene carbonate and diethyl carbonate. The electrochemical performance of this IL has been demonstrated using a cathode consisting of ball-milled LiMn2O4 particles. A direct comparison of the ionic liquid electrolyte with the nonionic low-viscosity conventional solvent blend is presented.

Polymer Microspheres Prepared by Water-Borne Thiol-Ene Suspension Photopolymerization.

Thiol-ene polymerizations are shown to be possible in a water-borne suspension-like photopolymerization and yield spherical particles that have diameters in the range of submicrometers to hundreds of micrometers. This is the first report of such colloidal thiol-ene polymerizations. Thiol-ene polymerization offers unique conditions not commonly associated with a water-borne polymerization including a step-growth polymerization mechanism along with photoinitiation under ambient conditions. Example polymerizations of a triene, 3,5-triallyl-1,3,5-triazine-2,4,6 (1N,3H,5H)-trione (TTT), and a tetrathiol, pentaerythritol tetrakis(3-mercaptopropionate) (PETMP), with the photoinitiator 1-hydroxycyclohexyl phenyl ketone, surfactant sodium dodecyl sulfate (SDS), and a cosolvent (chloroform or toluene) are discussed. Various experimental parameters were examined such as surfactant concentration, homogenization energy, cosolvent species, and cosolvent amount in order to develop an understanding of the mechanism of microsphere formation. It is demonstrated that particle size is dependent on homogenization energy, with greater mechanical shear yielding smaller particles. In addition, higher concentrations of surfactant or solvent also produced smaller spherical particles. These observations lead to the conclusion that the particles are formed via a suspension-like polymerization.

Antimicrobial behavior of semifluorinated-quaternized triblock copolymers against airborne and marine microorganisms.

Semifluorinated-quaternized triblock copolymers (SQTCs) were synthesized by chemical modification of polystyrene-block-poly(ethylene-ran-butylene)-block-polyisoprene ABC triblock copolymers. Surface characterization of the polymers was performed by X-ray photoelectron spectroscopy (XPS) and near-edge X-ray absorption fine structure (NEXAFS) analysis. The surface of the SQTC showed very high antibacterial activity against the airborne bacterium Staphylococcus aureus with >99 % inhibition of growth. In contrast in marine fouling assays, zoospores of the green alga Ulva settled on the SQTC, which can be attributed to the positively charged surface. The adhesion strength of sporelings (young plants) of Ulva and Navicula diatoms (a unicellular alga) was high. The SQTC did not show marked algicidal activity.

ABC triblock surface active block copolymer with grafted ethoxylated fluoroalkyl amphiphilic side chains for marine antifouling/fouling-release applications.

An amphiphilic triblock surface-active block copolymer (SABC) possessing ethoxylated fluoroalkyl side chains was synthesized through the chemical modification of a polystyrene-block-poly(ethylene-ran-butylene)-block-polyisoprene polymer precursor. Bilayer coatings on glass slides consisting of a thin layer of the amphiphilic SABC spray coated on a thick layer of a polystyrene-block-poly(ethylene-ran-butylene)-block-polystyrene (SEBS) thermoplastic elastomer were prepared for biofouling assays with the green alga Ulva and the diatom Navicula. Dynamic water contact angle analysis and X-ray photoelectron spectroscopy (XPS) were used to characterize the surfaces. Additionally, the effect of the Young's modulus of the coating on the release properties of sporelings (young plants) of the green alga Ulva was examined through the use of two different SEBS thermoplastic elastomers possessing modulus values of an order of magnitude in difference. The amphiphilic SABC was found to reduce the settlement density of zoospores of Ulva as well as the strength of attachment of sporelings. The attachment strength of the sporelings was further reduced for the amphiphilic SABC on the "low"-modulus SEBS base layer. The weaker adhesion of diatoms, relative to a PDMS standard, further highlights the antifouling potential of this amphiphilic triblock hybrid copolymer.

Settlement of Ulva zoospores on patterned fluorinated and PEGylated monolayer surfaces.

Various designs for coatings that resist the attachment of marine organisms are based on the concept of "ambiguous" surfaces that present both hydrophobic and hydrophilic functionalities as surface domains. In order to facilitate the optimal design of such surfaces, information is needed on the scale of the domains that the settling stages of marine organisms are able to distinguish. Previous experiments showed that Ulva zoospores settle (attach) in high numbers onto fluorinated monolayers compared to PEGylated monolayers. The main aim of the present study was to determine, when zoospores of the green alga Ulva are presented with a choice of fluorinated or PEGylated surfaces, what the minimum dimensions of the two types of surface are that zoospores can detect and consequently settle on. Silicon wafers were chemically modified to produce a pattern of squares containing alternating fluorinated and PEGylated stripes of different widths on either a uniform fluorinated or PEGylated background. Each 1 cm x 1 cm square contained stripes with widths of 500, 200, 100, 50, 20, 5, or 2 microm as well as an unpatterned square with a chemistry opposite that of the background. Spores were selective in choosing where to settle, settling at higher densities on fluorinated stripes compared to PEGylated stripes. However, the magnitude of response, and the consequences for settlement on patterned areas overall, was dependent on both the width of the stripes and the chemistry of the background. The data are discussed in relation to the ability of spores to "choose" favorable sites for settlement and the implications for the development of novel antifouling coatings.

Patterned biofunctional poly(acrylic acid) brushes on silicon surfaces.

Protein patterning was carried out using a simple procedure based on photolithography wherein the protein was not subjected to UV irradiation and high temperatures or contacted with denaturing solvents or strongly acidic or basic solutions. Self-assembled monolayers of poly(ethylene glycol) (PEG) on silicon surfaces were exposed to oxygen plasma through a patterned photoresist. The etched regions were back-filled with an initiator for surface-initiated atom transfer radical polymerization (ATRP). ATRP of sodium acrylate was readily achieved at room temperature in an aqueous medium. Protonation of the polymer resulted in patterned poly(acrylic acid) (PAA) brushes. A variety of biomolecules containing amino groups could be covalently tethered to the dense carboxyl groups of the brush, under relatively mild conditions. The PEG regions surrounding the PAA brush greatly reduced nonspecific adsorption. Avidin was covalently attached to PAA brushes, and biotin-tagged proteins could be immobilized through avidin-biotin interaction. Such an immobilization method, which is based on specific interactions, is expected to better retain protein functionality than direct covalent binding. Using biotin-tagged bovine serum albumin (BSA) as a model, a simple strategy was developed for immobilization of small biological molecules using BSA as linkages, while BSA can simultaneously block nonspecific interactions.

Surface organization, light-driven surface changes, and stability of semifluorinated azobenzene polymers.

A series of polymers with 4-perfluoroalkyl-modified azobenzene side groups was investigated for its light-induced changes in surface properties. The ultraviolet (UV) light activated trans to cis isomerization of the azobenzene group, and the influence of molecular order and orientation on this process were studied using near-edge X-ray absorption fine structure (NEXAFS) spectroscopy and water contact angle measurements. Light-induced molecular reorganization in the near-surface region was studied by NEXAFS using in situ UV irradiation of polymer thin films. Differential scanning calorimetry and wide-angle X-ray scattering studies showed that sufficiently long fluoroalkyl groups formed well-ordered smectic mesophases in the bulk, as well as on the surface, which was evidenced by NEXAFS. The disruption of mesogen packing by photoisomerization was found to be influenced by the fluoroalkyl segment length. Surfaces with perfluorohexyl and perfluorooctyl groups that showed high orientational order were also highly resistant to light-induced changes. In such cases, the trans-cis isomerization resulted in greater lowering of the azobenzene phenyl ring order parameters than the perfluoroalkyl order parameters. UV exposure caused reorientation of the phenyl rings of the azobenzene group, but the terminal perfluoroalkyl segments remained more or less ordered.

Surfaces of fluorinated pyridinium block copolymers with enhanced antibacterial activity.

Polystyrene-b-poly(4-vinylpyridine) copolymers were quaternized with 1-bromohexane and 6-perfluorooctyl-1-bromohexane. Surfaces prepared from these polymers were characterized by contact angle measurements, near-edge X-ray absorption fine structure spectroscopy and X-ray photoelectron spectroscopy. The fluorinated pyridinium surfaces showed enhanced antibacterial activity compared to their nonfluorinated counterparts. Even a polymer with a relatively low molecular weight pyridinium block showed high antimicrobial activity. The bactericidal effect was found to be related to the molecular composition and organization in the top 2-3 nm of the surface and increased with increasing hydrophilicity and pyridinium concentration of the surface.

Comparison of the fouling release properties of hydrophobic fluorinated and hydrophilic PEGylated block copolymer surfaces: attachment strength of the diatom Navicula and the green alga Ulva.

To understand the role of surface wettability in adhesion of cells, the attachment of two different marine algae was studied on hydrophobic and hydrophilic polymer surfaces. Adhesion of cells of the diatom Navicula and sporelings (young plants) of the green macroalga Ulva to an underwater surface is mainly by interactions between the surface and the adhesive exopolymers, which the cells secrete upon settlement and during subsequent colonization and growth. Two types of block copolymers, one with poly(ethylene glycol) side-chains and the other with liquid crystalline, fluorinated side-chains, were used to prepare the hydrophilic and hydrophobic surfaces, respectively. The formation of a liquid crystalline smectic phase in the latter inhibited molecular reorganization at the surface, which is generally an issue when a highly hydrophobic surface is in contact with water. The adhesion strength was assessed by the fraction of settled cells (Navicula) or biomass (Ulva) that detached from the surface in a water flow channel with a wall shear stress of 53 Pa. The two species exhibited opposite adhesion behavior on the same sets of surfaces. While Navicula cells released more easily from hydrophilic surfaces, Ulva sporelings showed higher removal from hydrophobic surfaces. This highlights the importance of differences in cell-surface interactions in determining the strength of adhesion of cells to substrates.

Anti-biofouling properties of comblike block copolymers with amphiphilic side chains.

Surfaces of novel block copolymers with amphiphilic side chains were studied for their ability to influence the adhesion of marine organisms. The surface-active polymer, obtained by grafting fluorinated molecules with hydrophobic and hydrophilic blocks to a block copolymer precursor, showed interesting bioadhesion properties. Two different algal species, one of which adhered strongly to hydrophobic surfaces, and the other, to hydrophilic surfaces, showed notably weak adhesion to the amphiphilic surfaces. Both organisms are known to secrete adhesive macromolecules, with apparently different wetting characteristics, to attach to underwater surfaces. The ability of the amphiphilic surface to undergo an environment-dependent transformation in surface chemistry when in contact with the extracellular polymeric substances is a possible reason for its antifouling nature. Near-edge X-ray absorption fine structure spectroscopy (NEXAFS) was used, in a new approach based on angle-resolved X-ray photoelectron spectroscopy (XPS), to determine the variation in chemical composition within the top few nanometers of the surface and also to study the surface segregation of the amphiphilic block. A mathematical model to extract depth-profile information from the normalized NEXAFS partial electron yield is developed.

Fluorinated polymers: liquid crystalline properties and applications in lithography.

Fluorinated polymers form an interesting class of materials with a wealth of unique properties including self-assembly, remarkably low surface energies, low absorbance to 157 nm UV light, and solubility in supercritical carbon dioxide. As a result many fluorinated polymers are of use in advanced technology applications. We review some of our work on the synthesis and characterization of block copolymers with fluorinated side chains, with special emphasis on surfaces formed using these polymers. The use of fluorinated polymers as photoresists for 157 nm lithography, with the possibility for processing in environmentally friendly supercritical carbon dioxide is also discussed.