Electrolytes for Zn Batteries: Deep Eutectic Solvents in Polymer Gels.

Gel polymer electrolytes composed of deep eutectic solvent acetamide :Zn(TFSI) and poly(ethylene oxide) (PEO) are prepared by using a fast, solvent-free procedure. The effect of the PEO molecular weight and its concentration on the physicochemical and electrochemical properties of the electrolytes are studied. Gels prepared with ultrahigh molecular-weight PEO present pseudo-solid behavior and ionic conductivity even higher than that of the original liquid electrolyte.

Highly Stable Hierarchically Structured All-Polymeric Lubricant-Infused Films Prevent Thrombosis and Repel Multidrug-Resistant Pathogens.

Thrombus formation and infections caused by bacterial adhesion are the most common causes of failure in blood-contacting medical devices. Reducing the interaction of pathogens using repellent surfaces has proven to be a successful strategy in preventing device failure. However, designing scale-up methodologies to create large-scale repellent surfaces remains challenging.

Ionic Conductivity Enhancement in UHMW PEO Gel Electrolytes Based on Room-Temperature Ionic Liquids and Deep Eutectic Solvents.

Physical gels made of poly(ethylene oxide) (PEO) and deep eutectic solvents urea-Li bis(trifluoromethanesulfonyl)imide (TFSI) and ethylene glycol/LiTFSI, or pyrrolidinium ionic liquid solutions PYR13TFSI-LiTFSI and PYR14TFSI-LiTFSI, are prepared by a fast, single-step process, which involves no auxiliary solvents or intermediates and is reproducible and scalable. The properties of these gels are studied as a function of the PEO content and its molecular weight and the nature of the liquid electrolyte. The gels prepared with a low concentration (1-5 wt %) of ultrahigh molecular weight (UHMW) PEO are tough, stretchable materials which resemble soft elastomers and are also self-healing and transparent.

Addressing Manufacturability and Processability in Polymer Gel Electrolytes for Li/Na Batteries.

Gel electrolytes are prepared with Ultra High Molecular Weight (UHMW) polyethylene oxide (PEO) in a concentration ranging from 5 to 30 wt.% and Li- and Na-doped 1-butyl-1-methylpyrrolidinium bis(trifluoromethylsulfonyl)imide (PYR14-TFSI) by a simple procedure consisting of dissolving PEO by melting it directly in the liquid electrolyte while stirring the blend. This procedure is fast, reproducible and needs no auxiliary solvents, which makes it sustainable and potentially easy to scale up for mass production.

Chloroaluminate Gel Electrolytes Prepared with Copolymers Based on Imidazolium Ionic Liquids and Deep Eutectic Solvent AlCl:Urea.

Polymer gel electrolytes (PGEs) have been prepared with copolymers based on imidazolium ionic liquids and the deep eutectic mixture of AlCl:urea (uralumina) as liquid electrolyte. The copolymers were synthesized by photopolymerization of vinylpirrolidone or methylmethacrylate with imidazolium bis (trifluoromethane sulfonyl) imide (TFSI) ionic liquid monomer and mixed in an increasing range of wt.% with uralumina.

Understanding the Molecular Structure of the Elastic and Thermoreversible AlCl : Urea/Polyethylene Oxide Gel Electrolyte.

It is possible to prepare elastic and thermoreversible gel electrolytes with significant electroactivity by dissolving minimal weight fractions of ultra-high molecular weight polyethylene oxide (UHMW PEO) in an aluminum deep eutectic solvent (DES) electrolyte composed of AlCl and urea at a molar ratio of 1.5 : 1 (AlCl /urea). The experimental vibrational spectra (FTIR and Raman) provide valuable information on the structure and composition of the gel electrolyte.

Tough Polymer Gel Electrolytes for Aluminum Secondary Batteries Based on Urea: AlCl, Prepared by a New Solvent-Free and Scalable Procedure.

Polymer gel electrolytes have been prepared with polyethylene oxide (PEO) and the deep eutectic mixture of AlCl: urea (uralumina), a liquid electrolyte which has proved to be an excellent medium for the electrodeposition of aluminum. The polymer gel electrolytes are prepared by mixing PEO in the liquid electrolyte at T > 65 °C, which is the melting point of PEO. This procedure takes a few minutes and requires no subsequent evaporation steps, being a solvent-free, and hence more sustainable procedure as compared to solvent-mediated ones.

Solvent-Free and Scalable Procedure to Prepare PYR13TFSI/LiTFSI/PVDF⁻HFP Thermoplastic Electrolytes with Controlled Phase Separation and Enhanced Li Ion Diffusion.

Solid electrolytes for Li transport have been prepared by melt-compounding in one single step. Electrolytes are composed of polyvinylidene fluoride-hexafluoropropylene (PVDF-HFP) with PYR13TFSI on its own or with varying concentration of LiTFSI. While the extrusion of PVDF-HFP with PYR13TFSI is possible up to relatively high liquid fractions, the compatibility of PVDF-HFP with LiTFSI/PYR13TFSI solutions is much lower.

Solvent-Free Procedure for the Preparation under Controlled Atmosphere Conditions of Phase-Segregated Thermoplastic Polymer Electrolytes.

A solvent-free method that allows thermoplastic solid electrolytes based on poly(ethylene oxide) PEO to be obtained under controlled atmosphere conditions is presented. This method comprises two steps, the first one being the melt compounding of PEO with a filler, able to physically crosslink the polymer and its pelletizing, and the second the pellets' swelling with an electroactive liquid phase. This method is an adaptation of the step described in previous publications of the preparation of thermoplastic electrolytes by a single melt compounding.

High Performance Polymer/Ionic Liquid Thermoplastic Solid Electrolyte Prepared by Solvent Free Processing for Solid State Lithium Metal Batteries.

A polymer/ionic liquid thermoplastic solid electrolyte based on poly(ethylene oxide) (PEO), modified sepiolite (TPGS-S), lithium bis(trifluoromethanesulfonyl)imide (LiTFSI), and 1-Butyl-1-methylpyrrolidinium bis(trifluoromethanesulfonyl)imide (PYRTFSI) ionic liquid is prepared using solvent free extrusion method. Its physical-chemical, electrical, and electrochemical properties are comprehensively studied. The investigated solid electrolyte demonstrates high ionic conductivity together with excellent compatibility with lithium metal electrode.

Ionic Liquid-Based Thermoplastic Solid Electrolytes Processed by Solvent-Free Procedures.

A series of thermoplastic polymer electrolytes have been prepared employing poly(ethylene oxide) (PEO) as a polymer matrix, bis(trifluoromethane sulfonimide) (LiTFSI), and different room-temperature ionic liquids (RTIL) with bis(fluorosulfonyl)imide (FSI) or TFSI anions. This formulation makes them safe and non-flammable. The electrolytes have been processed in the absence of solvents by melt compounding at 120 °C, using sepiolite modified with d-α-tocoferol-polyethyleneglycol 1000 succinate (TPGS-S) as a physical cross-linker of PEO.

Long-Term Underwater Hydrophobicity: Exploring Topographic and Chemical Requirements.

A family of hybrid organoinorganic silica-based particles with varied chemical natures and morphologies has been synthesized to test their ability to develop coatings with underwater hydrophobicity. The particles were characterized by elemental microanalysis, scanning electron microscopy, and dynamic light scattering to evaluate the organic content, observe the morphology, and estimate the aggregate size, respectively. These morphologies were transferred into surface topographies by spraycoating dispersions made from the particles onto glass supports, resulting in coatings with an ample range of profiles and roughness but all of them being superhydrophobic.

Superhydrophobic and highly luminescent polyfluorene/silica hybrid coatings deposited onto glass and cellulose-based substrates.

Neat poly(9,9-dioctyl-9H-fluorene) (PFO) and composites of PFO and a modified organonanosilica P(7) at weight ratios 90/10, 70/30, and 50/50 have been employed to prepare fluorescent and superhydrophobic coatings by spraying onto three different substrates: glass, Whatman paper, and a filtration membrane of mixed cellulose esters. The water repellency of the coatings and their photophysical properties are therein studied. It is found that, irrespective of the substrate and the composite composition, all coatings remain fluorescent.

Ion diffusion coefficients model and molar conductivities of ionic salts in aprotic solvents.

In the study of the electric properties of electrolytes, the determination of the diffusion coefficients of the species that intervene in the charge transport process is of great importance, particularly that of the free ions (D(+) and D(-)), the only species that contribute to the conductivity. In this work we propose a model that allows, with reasonable assumptions, determination of D(+) and D(-), and the degree of dissociation of the salt, α, at different concentrations, using the diffusion coefficients experimentally obtained with NMR. Also, it is shown that the NMR data suffice to estimate the conductivity of the electrolytes.

Multipurpose ultra and superhydrophobic surfaces based on oligodimethylsiloxane-modified nanosilica.

Nonfluorinated hydrophobic surfaces are of interest for reduced cost, toxicity, and environmental problems. Searching for such surfaces together with versatile processing, A200 silica nanoparticles are modified with an oligodimethylsiloxane and used by themselves or with a polymer matrix. The goal of the surface modification is controlled aggregate size and stable suspensions.

Surface modification of sepiolite in aqueous gels by using methoxysilanes and its impact on the nanofiber dispersion ability.

Surface modification reactions on needle-like sepiolite using alkyl and functional silanes have been carried out in the form of aqueous gels. In contrast with modifications in organic solvents, reactions in water make it possible to modify the surface of almost-individual sepiolite fibers and produce either a continuous coating or a nanotexturization of the sepiolite fiber surface, depending on the reaction conditions. This clean procedure substitutes advantageously organic solvent surface modifications and allows the tuning of surface properties such as specific surface area, wetting behavior, and chemical functionalization.

Microwave versus conventional heating in the grafting of alkyltrimethoxysilanes onto silica particles.

The scope of this work is the comparative analysis in terms of grafting rate, structure of the grafted layer, and wetting behavior of three series of silica nanoparticles modified with alkyltrimethoxysilanes by using conventional heating with and without acid catalysis, and microwave irradiation. A comprehensive characterization of the grafted layer by means of Fourier transform infrared (FTIR), microanalysis, and solid state NMR techniques has shown that microwave irradiation provokes a pronounced increase in the loading rate compared to conventional heating. This microwave effect is outstanding in the case of the reactions with methyltrimethoxysilane, because of the acceleration of the condensation rate.

Effect of microstructure on the thermo-oxidation of solid isotactic polypropylene-based polyolefins.

In the present work we aim to clarify the role of the microstructure and the crystalline distribution from the thermo-oxidation of solid isotactic PP (iPP) and ethylene-propylene (EP) copolymers. The effects of the content and quality of the isotacticity interruptions, together with the associated average isotactic length, on the induction time (t) as well as on the activation energy (E) of the thermo-oxidation are analysed. Both parameters have been found to change markedly at an average isotactic length () of 30 propylene units.

Use of p-toluenesulfonic acid for the controlled grafting of alkoxysilanes onto silanol containing surfaces: preparation of tunable hydrophilic, hydrophobic, and super-hydrophobic silica.

The modification of Aerosil 200 has been carried out using methoxysilanes in toluene reflux, with p-toluenesulfonic acid as the catalyst. Both trimethoxyalkyl silanes (methyl, ethyl, propyl, butyl, hexyl, octyl, and octadecyl) and trialkylmethoxy silanes (trimethyl and dimethyloctyl) have been used. The surface has been studied by 29Si NMR, 13C NMR, elemental analysis, thermogravimetry, water contact angle, and BET analysis.

A potentiostatic study of oxygen transport through poly(2-ethoxyethyl methacrylate-co-2,3-dihydroxypropylmethacrylate) hydrogel membranes.

The oxygen permeability and diffusion coefficients of hydrogel membranes prepared with copolymers of 2-ethoxyethyl methacrylate (EEMA)/2,3-dihydroxypropylmethacrylate (MAG) with mole fraction of the second monomer in the range between 0 and 0.75 are described. Values of the permeability and diffusion coefficients of oxygen are determined by using electrochemical procedures involving the measurement of the steady-state current in membranes prepared by radical polymerization of the monomers.