Transport in polymer-gel composites: Theoretical methodology and response to an electric field

A theoretical model of electromigrative, diffusive and convectivetransport polymer-gel composites is presented. Bulk properties are derived from the standard electrokinetic model with an impenetrable charged sphere embedded in an electrolyte-saturated Brinkman medium. Because the microstructure can be carefully controlled, these materials are promising candidates for enhanced gel-electrophoresis, chemical sensing, drug delivery, and microfluidic pumping technologies. The methodology provides `exact' solutions for situations where perturbations from equilibrium are induced by gradients of electrostatic potential, concentration and pressure. While the volume fraction of the inclusions should be small, Maxwell's well-known theory of conduction suggests that the theory may also be accurate at moderate volume fractions. In this work, the model is used to compute ion fluxes, electrical current density, and convective flow induced by an applied electric field. The electric-field-induced (electro-osmotic) flow is a sensitive indicator of the inclusion zeta-potential and size, electrolyte concentration, and Darcy permeability of the gel, while the electrical conductivity increment is most often independent of the polymer gel, and is much less sensitive to particle and electrolyte characteristics

Preliminary test on modified clays for seawater resistant drilling fluids

The quality of a drilling fluid declines in salt water conditions. An engineered clay (HYPER clay) was developed for geosynthetic clay liners with enhanced resistance to aggressive conditions. This study investigates the potential of this superior clay for drilling fluids applied in salt water conditions. A sodium bentonite was treated with a carboxymethyl cellulose (CMC) polymer following the HYPER clay process method. Preliminary tests were performed to investigate suitability of HYPER clay for seawater resistant drilling fluids. Fluid performance was characterized by its thixotropic behavior, rheological properties (gel strength, yield point and viscosity), swell and bleeding behavior. Drilling fluid performance was analyzed at various polymer dosages and electrolyte concentrations. Polymer treatment improved the gel strength and swelling ability of the fluid, especially in electrolyte solutions. Moreover, filter press tests (API 13B-1, 76% seawater) showed that filtrate loss decreased due to polymer treatment

Honeycomb-like porous gel polymer electrolyte membrane for lithium ion batteries with enhanced safety

Lithium ion batteries have shown great potential in applications as power sources for electric vehicles and large-scale energy storage. However, the direct uses of flammable organic liquid electrolyte with commercial separator induce serious safety problems including the risk of fire and explosion. Herein, we report the development of poly(vinylidene difluoride-co-hexafluoropropylene) polymer membranes with multi-sized honeycomb-like porous architectures. The as-prepared polymer electrolyte membranes contain porosity as high as 78%, which leads to the high electrolyte uptake of 86.2 wt%. The PVDF-HFP gel polymer electrolyte membranes exhibited a high ionic conductivity of 1.03 mS cm -1 at room temperature, which is much higher than that of commercial polymer membranes. Moreover, the as-obtained gel polymer membranes are also thermally stable up to 3506C and non-combustible in fire (fire-proof). When applied in lithium ion batteries with LiFePO4 as cathode materials, the gel polymer electrolyte demonstrated excellent electrochemical performances. This investigation indicates that PVDF-HFP gel polymer membranes could be potentially applicable for high power lithium ion batteries with the features of high safety, low cost and good performance

In-situ measurements of the optical absorption of dioxythiophene-based conjugated polymers

Conjugated polymers can be reversibly doped by electrochemical means. This doping introduces new sub-bandgap optical absorption bands in the polymer while decreasing the bandgap absorption. To study this behavior, we have prepared an electrochemical cell allowing measurements of the optical properties of the polymer. The cell consists of a thin polymer film deposited on gold-coated Mylar behind which is another polymer that serves as a counterelectrode. An infrared transparent window protects the upper polymer from ambient air. By adding a gel electrolyte and making electrical connections to the polymer-on-gold films, one may study electrochromism in a wide spectral range. As the cell voltage (the potential difference between the two electrodes) changes, the doping level of the conjugated polymer films is changed reversibly. Our experiments address electrochromism in poly(3,4-ethylene-dioxy-thiophene) (PEDOT) and poly(3,4-dimethyl-propylene-dioxy-thiophene) (PProDOT-Me$_2$). This closed electrochemical cell allows the study of the doping induced sub-bandgap features (polaronic and bipolaronic modes) in these easily oxidized and highly redox switchable polymers. We also study the changes in cell spectra as a function of polymer thickness and investigate strategies to obtain cleaner spectra, minimizing the contributions of water and gel electrolyte features

Electric-field-induced displacement of a charged spherical colloid embedded in an elastic Brinkman medium

When an electric field is applied to an electrolyte-saturated polymer gel embedded with charged colloidal particles, the force that must be exerted by the hydrogel on each particle reflects a delicate balance of electrical, hydrodynamic and elastic stresses. This paper examines the displacement of a single charged spherical inclusion embedded in an uncharged hydrogel. We present numerically exact solutions of coupled electrokinetic transport and elastic-deformation equations, where the gel is treated as an incompressible, elastic Brinkman medium. This model problem demonstrates how the displacement depends on the particle size and charge, the electrolyte ionic strength, and Young's modulus of the polymer skeleton. The numerics are verified, in part, with an analytical (boundary-layer) theory valid when the Debye length is much smaller than the particle radius. Further, we identify a close connection between the displacement when a colloid is immobilized in a gel and its velocity when dispersed in a Newtonian electrolyte. Finally, we describe an experiment where nanometer-scale displacements might be accurately measured using back-focal-plane interferometry. The purpose of such an experiment is to probe physicochemical and rheological characteristics of hydrogel composites, possibly during gelation

Partitioning of a polymer chain between a confining cavity and a gel

A lattice field theory approach to the statistical mechanics of charged polymers in electrolyte solutions [S. Tsonchev, R. D. Coalson, and A. Duncan, Phys. Rev. E 60, 4257, (1999)] is applied to the study of a polymer chain contained in a spherical cavity but able to diffuse into a surrounding gel. The distribution of the polymer chain between the cavity and the gel is described by its partition coefficient, which is computed as a function of the number of monomers in the chain, the monomer charge, and the ion concentrations in the solution.Comment: 17 pages, 6 figure

Polyacrylonitrile-Nanofiber-Based Gel Polymer Electrolyte for Novel Aqueous Sodium-Ion Battery Based on a Na4Mn9O18 Cathode and Zn Metal Anode

A gel polymer electrolyte was formed by trapping an optimized Na+/Zn2+ mixed-ion aqueous electrolyte in a polyacrylonitrile nanofiber polymer matrix. This electrolyte was used in a novel aqueous sodium-ion battery (ASIB) system, which was assembled by using a zinc anode and Na4Mn9O18 cathode. The nanorod-like Na4Mn9O18 was synthesized by a hydrothermal soft chemical reaction. The structural and morphological measurement confirmed that the highly crystalline Na4Mn9O18 nanorods are uniformly distributed. Electrochemical tests of Na4Mn9O18//Zn gel polymer battery demonstrated its high cycle stability along with a good rate of performance. The battery delivers an initial discharge capacity of 96 mAh g−1 , and 64 mAh g−1 after 200 cycles at a high cycling rate of 1 C. Our results demonstrate that the Na4Mn9O18//Zn gel polymer battery is a promising and safe high-performance battery

Investigation of polymers used in lithium oxygen batteries as electrolyte and cathode materials

University of Technology, Sydney. Faculty of Science.It has been well established that the electrolytes and cathodes have a significant effect on the electrochemical performance of lithium oxygen batteries. In this Master project, polymers were employed as electrolyte and cathode materials due to their unique superior properties. Using different methods, we synthesized suitable gel polymer electrolytes and conducting polymer catalysts for lithium oxygen batteries. Techniques such as field emission gun scanning electron microscopy, X-ray diffraction, and Fourier transform infrared spectroscopy were used to characterize the physical properties. Electrochemical analyses including the galvanostatic discharge and charge method, the cyclic voltammetry, the linear sweep voltammetry and the impedance spectra were conducted to determine the electrochemical performance for the as-prepared materials. Gel polymer electrolytes based on low molecular weight polyethylene glycol were prepared and used as electrolyte in lithium oxygen batteries. The as-prepared polymer electrolytes showed improved stability compared with liquid electrolytes and exhibited good performance in lithium oxygen batteries. Additionally, the addition of ceramic filler SiO₂ was found to reduce the stability of polymer electrolyte towards oxygen reduction reaction although higher ionic conductivity was obtained. Polyethylene glycol based gel polymer electrolyte without SiO₂ addition exhibited excellent cycling performance and it could be used for achieving long-life lithium oxygen batteries. Poly(vinylidene fluoride-co-hexafluoropropylene) based gel polymer electrolytes were prepared by solvent casting and employed as electrolytes in lithium oxygen batteries. The stability of the gelled electrolyte with tetraethylene glycol dimethyl ether has been greatly increased than the liquid one. The as-prepared polymer electrolyte was demonstrated excellent cycling performances. This thesis also investigated the effect of different plasticizers on the performance of lithium oxygen batteries. The reason could lie on the interactions among the components when the gelled structure was set. The tetraethylene glycol dimethyl ether based gel polymer electrolyte showed the best electrochemical performance and can be used for long-life lithium oxygen batteries. Polypyrrole conducting polymers with different dopants have been synthesized and applied as the cathode catalysts in lithium oxygen batteries. Polypyrrole polymers exhibited an effective catalytic activity for oxygen reduction in lithium oxygen batteries. It was discovered that dopant significantly influenced the electrochemical performance of polypyrrole. The polypyrrole doped with Cl⁻ demonstrated higher capactity and more stable cyclability than that doped with ClO₄⁻. Polypyrrole conducting polymers also exhibited higher capacity and better cycling performance than that of carbon catalyst. Conducting polymer coated carbon nanotubes were synthesized and used as catalysts in lithium oxygen batteries. It was found that both polypyrrole and poly(3,4-ethylenedioxythiophene) coated carbon nanotubes could provide high cycling performance while polypyrrole based one exhibited higher capacities. The ratio of conducting polymer coating also affected the electrochemical performance of lithium oxygen batteries. The conducting polymer coated carbon nanotubes also showed better performance than the bare carbon nanotubes

Poly(vinylidene fluoride-hexafluoropropylene) polymer electrolyte for paper-based and flexible battery applications

Paper-based batteries represent a new frontier in battery technology. However, low-flexibility and poor ionic conductivity of solid electrolytes have been major impediments in achieving practical mechanically flexible batteries. This work discuss new highly ionic conductive polymer gel electrolytes for paper-based battery applications. In this paper, we present a poly(vinylidene fluoride-hexafluoropropylene) (PVDH-HFP) porous membrane electrolyte enhanced with lithium bis(trifluoromethane sulphone)imide (LiTFSI) and lithium aluminum titanium phosphate (LATP), with an ionic conductivity of 2.1 × 10−3 S cm−1. Combining ceramic (LATP) with the gel structure of PVDF-HFP and LiTFSI ionic liquid harnesses benefits of ceramic and gel electrolytes in providing flexible electrolytes with a high ionic conductivity. In a flexibility test experiment, bending the polymer electrolyte at 90° for 20 times resulted in 14% decrease in ionic conductivity. Efforts to further improving the flexibility of the presented electrolyte are ongoing. Using this electrolyte, full-cell batteries with lithium titanium oxide (LTO) and lithium cobalt oxide (LCO) electrodes and (i) standard metallic current collectors and (ii) paper-based current collectors were fabricated and tested. The achieved specific capacities were (i) 123 mAh g−1 for standard metallic current collectors and (ii) 99.5 mAh g−1 for paper-based current collectors. Thus, the presented electrolyte has potential to become a viable candidate in paper-based and flexible battery applications. Fabrication methods, experimental procedures, and test results for the polymer gel electrolyte and batteries are presented and discussed

Synthesis and Characterization of PMMA based polymer gel electrolyte

PMMA based Polymer Gel Electrolytes have been prepared with different concentrations of salt (NaI) by gelation method. This study has been carried out to understand the effect of salt concentration on conductivity of polymer gel electrolyte. The prepared samples are characterized by XRD, optical microscopy, FTIR and Dielectric spectroscopy. The XRD studies revealed that the prepared polymer gel electrolyte samples are semi-crystalline in nature. Optical Microscopy study confirmed the results obtained from the XRD analysis. FTIR Spectroscopy study indicated the bands present in the samples were not affected for different salt concentration, which indicates that the polymer does not participate in the complexation process. The dielectric and electrical properties of the material were studied by the dielectric spectroscopic technique in a wide frequency range at room temperature. The d. c. conductivity of samples was calculated using complex impedance plots