Structural,Electrical and Optical Characterization of Pure and Doped Poly (Vinyl Alcohol) (PVA) Polymer Electrolyte Films

A sodium ion conducting polymer electrolyte based on Poly (Vinyl Alcohol) (PVA) complexed with Sodium Iodide (NaI) was prepared using solution cast technique. The structural properties of composite PVA polymer electrolyte films were examined by XRD. The XRD results revealed that the amorphous domains of PVA polymer matrix increased in size with the increase of NaI salt concentration. The variation in film morphology was examined by scanning electron microscopy. FT-IR spectra studies for pure PVA and complexed films revealed the vibrational changes that occurred due to the effect of dopant salt in the polymer. DC conductivity was measured in the temperature range of 303–373° K and the conductivity was found to increase with the increase of dopant concentration as well as temperature. Optical absorption studies were made in the wavelength range 200–600 nm. The absorption edge, direct band gap, and indirect band gap values were evaluated.     

Characterization of poly(vinyl alcohol)/potassium chloride polymer electrolytes for electrochemical cell applications

A solid polymer electrolyte system based on poly(vinyl alcohol) (PVA) complexed with potassium chloride (KCl) salt was prepared by using solution cast technique. The complexation of KCl salt with the polymer was confirmed by X‐ray diffractrometer and Fourier transform infrared spectroscopy. Differential scanning calorimetry was used to determine the melting temperatures and crystallinity of the pure PVA and complexed films. Ionic conductivities of the electrolytes have been determined by AC impedance studies in the temperature range 303–373 K. The conductivity was found to increase with the increase in dopant concentration and temperature. Transference number data suggests that the charge transport in this polymer electrolyte system is mainly due to ions. Optical absorption studies were made in the wavelength range 200–800 nm on pure and KCl doped PVA films. The absorption edge, direct band, and indirect band gap values were evaluated. It was found that the energy gaps and band edge values shifted to lower energies on doping. Electrochemical cells were fabricated with the configuration of K/(PVA + KCl)/(I₂ + C + electrolyte) and discharge characteristics were studied under a constant load of 100 kΩ. Various cell parameters, such as open circuit voltage, short circuit current, power density, and energy density were determined. POLYM. ENG. SCI., 2012. © 2012 Society of Plastics Engineers     

Optical and electrical characterization of (PEO+methyl violet) polymer electrolytes

Optical properties and electrical conductivity of polyethylene oxide (PEO) with methyl violet dopant film have studied. The complexation of the methyl violet dopant with PEO was confirmed by X‐ray diffraction (XRD) and Fourier transform infrared (FTIR) spectroscopic studies. The microstructure morphology have been analyzed by scanning electron microscope (SEM) for pure and dopant films. The UV‐absorption studies were made in the wavelength range 190–1100 nm for pure and doped films. The dc electrical conductivity data was collected using two probe technique in the temperature range 303–333 K. The UV–visible spectra showed the absorption band at 190 nm for pure PEO and doped from 208–224 nm region with different absorption intensities. The absorption edge, direct and indirect band gap were estimated using Mott and Davis Model. The optical activation energy can be determined using the Urbach rule, for pure PEO it was found 2.38 eV and 1.28–4.08 eV for doped films. The absorption band was shifted toward the higher frequency, the direct and indirect band gap decreases with increasing of dopant concentration, corresponds to the allowed inter band transition of electron. The dc electrical conductivity results shows that it increases with increasing dopant weight percentage and temperature which corresponds to the enhancement of charge mobility in these dye doped polymers. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Optical, electrical and discharge profiles for (PVC + NaIO4) polymer electrolytes

A sodium ion conducting polymer electrolyte based on poly (vinyl chloride) (PVC) complexed with NaIO₄ was prepared using a solution-cast technique. Optical properties such as direct and indirect optical energy gap, and optical absorption edge were investigated in pure and doped PVC films from their optical absorption spectra in the 200–600 nm wavelength region. The direct optical energy gap for pure PVC lies at 3.14 eV while it ranges from 2.60 to 3.45 eV for different composition doped films. Similar behavior was observed for the indirect optical energy gap and absorption edge. It was found that the energy gaps and band edge values shifted to higher energies on doping with NaIO₄ up to a dopant concentration of 10 wt%. Measurements of ionic conductivity and transference number were made to investigate the order of conductivity and charge transport in this polymer electrolyte. Transference number values show that the charge transport in this polymer electrolyte is predominantly due to ions (t _ion = 0.93). The conductivity increases with increase in concentration of the salt and with temperature. Using this electrolyte, cells were fabricated and their discharge profiles were studied under constant load. Miscibility studies were performed using X-ray diffraction (XRD) and Fourier Transform Infrared analysis (FT-IR) measurements.     

Structure,electrical and optical properties of (PVA/LiAsF6) polymer composite electrolyte films

In this work, Li⁺ ion conducting polymer composite electrolyte films (PECs) were prepared based on poly (vinyl alcohol) (PVA), lithium hexafluoro arsenate (LiAsF₆), and ceramic filler TiO₂ using solution cast technique. The XRD and FTIR spectra were used to determine the complexation of the PVA polymer with LiAsF₆ salt. The ionic conductivities of the (PVA + LiAsF₆) and (PVA + LiAsF₆ + TiO₂) films have been determined by the A.C. impedance measurements in the temperature range 320–440 K. The maximum conductivity was found to be 5.10 × 10^?4 S cm^?1 for PVA:LiAsF₆ (75:25) + 5 wt% TiO₂ polymer composite film at 320 K. The calculation of Li⁺ ion transference number was carried out by the combination of A.C. impedance and D.C. polarization methods and is found to be 0.52 for PVA:LiAsF₆ (75:25) + 5 wt% TiO₂ film. Optical properties such as direct energy gap, indirect energy gap, and optical absorption edge values were investigated in pure PVA and salt complexed PVA films from their optical absorption spectra in the wavelength range of 200–600 nm. The absorption edge was found at 5.76 eV for undoped film, while it is observed at 4.87 and 4.70 eV for 20 and 25 wt% LiAsF₆ doped films, respectively. The direct band gaps for these undoped and salt doped PVA films were found to be 5.40, 5.12, and 4.87 eV, respectively, whereas the indirect band gaps were determined as 4.75, 4.45, and 4.30 eV. POLYM. ENG. SCI., 2010. © 2009 Society of Plastics Engineers     

Preparation and characterization of PVP-based polymer electrolytes for solid-state battery applications

Sodium ion conducting polymer electrolyte films based on poly(vinyl pyrrolidone) (PVP) were prepared using solution casting technique. Structural characterization was performed using X-ray diffraction (XRD) technique. Increase in amorphous phase with the increase of dopant concentration was observed. Temperature dependence of electrical conductivity was performed using AC impedance analyzing technique in the frequency range of 0.1?KHz to 1?MHz. Activation energy values were evaluated, as well. Optical absorption studies were carried out in the wavelength range 200?C600?nm. Absorption edge, direct band gap, and indirect band gap values were also evaluated. Optical absorption edge and optical band gap (both direct and indirect) showed decreasing trend with increasing the concentration of the dopant. Dominant conducting species in the present electrolyte system was determined using Wagner polarization technique and dominant conducting species were found to be ions rather than electrons. Solid-state batteries were developed using the present solid polymer electrolyte system and discharge characteristics over the load of 100?k??. Cell parameters, e.g., open circuit voltage, short circuit current, current density, power density were evaluated, too. Among these cells, the cell made up of PVP/NaI (70/30) ratio for electrolyte was found to be more stable than the other two cells PVP/NaI (90/10) and (80/20) ratios and the obtained results were comparable with the results achieved by other studies.     

Structural,electrical and optical properties of pure and NaLaF<Subscript>4</Subscript> doped PEO polymer electrolyte films

A Sodium ion conducting polymer electrolyte based on Polyethylene oxide (PEO) complexed with Sodium lanthanum tetra fluoride (NaLaF₄) was prepared using solution cast technique. The complexation of the salt with PEO was confirmed by X-ray diffraction (XRD) and Fourier Transform Infrared spectroscopic (FTIR) studies. Differential Scanning Calorimetry (DSC) is carried out to determine the melting temperature of these electrolyte films. Electrical conductivity was measured in the temperature range 300–370 K as a function of dopant concentration as well as temperature. Optical absorption studies were made in the wavelength range 200–600 nm on pure and NaLaF₄ doped PEO film. The absorption edge was observed at 4.62 eV for undoped PEO while it ranged from 3.16 to 3.5 eV for NaLaF₄ doped films. The direct band gaps for undoped and NaLaF₄ doped PEO films were found to be, respectively, 4.54 and 3.44, 3.24 and 3.12 eV while the indirect band gaps were 4.43 and 3.25, 3.05 and 2.9 eV, respectively. It was found that the energy gaps and band edge values shifted to lower energies on doping with NaLaF₄ salt.     

Characterization of Lithium Ion-Conducting Blend Biopolymer Electrolyte Based on CH–MC Doped with LiBF<Subscript>4</Subscript>

Lithium ion-conducting polymer blend electrolytes based on chitosan and methylcellulose complexed with lithium tetrafluoroborate (LiBF₄) were prepared by a solution-casting method. The features of complexation of the solid polymer electrolytes were studied using X-ray diffraction techniques. Electrical conductivity of the prepared films was measured as a function of frequency at a different temperature. The increased trend of the electrical conductivity with increasing temperature and salt concentration can be attributed to increasing the mobility and number of lithium ions, respectively. The polymer electrolyte system exhibited Arrhenius-type, temperature-dependence ion conductivity behavior. Optical properties such as optical band gap, tail due to localized states and complex refractive index were estimated for present polymer electrolyte system from optical absorption measurement in the wavelength region 190–1100 nm. It was found that the optical direct band gap values shifted to lower energies upon addition of LiBF₄ salt up to 40 wt% dopant concentration, and showed an increasing tendency for a further increase in dopant concentration. The high refractive index for this composition (2.44–2.63) at visible wavelengths eminently suitable for optical applications.     

Evolution in the Electronic Structure of Polymer‐derived Amorphous Silicon Carbide

The electronic structure of polymer‐derived amorphous silicon carbide pyrolyzed at different temperatures was investigated by combining measurements of their temperature‐dependent conductivity and optical absorption. By comparing the experimental results with theoretical models, the parameters such as conduction band, band‐tail, defect energy, and Fermi energy were determined. The results revealed that band gap and band‐tail width decreased with increasing pyrolysis temperature. Furthermore, it was found that electrons transport followed a band‐tail hopping mechanism, rather than variable range hopping. These results were discussed in accordance with the microstructural evolutions of the material.     

Electrical and mechanical properties of multi‐walled carbon nanotubes reinforced PMMA and PS composites

The use of multi‐walled carbon nanotubes (MWCNT) as reinforcing material for thermoplastic polymer matrices, polymethyl methacrylate (PMMA), and polystyrene (PS) has been studied. MWCNT were synthesized by chemical vapor deposition (CVD) technique using ferrocene‐toluene mixture. As‐prepared nanotubes were ultrasonically dispersed in toluene and subsequently dispersed in PMMA and PS. Thin polymer composite films were fabricated by solvent casting. The effect of nanotube content on the electrical and mechanical properties of the nanocomposites was investigated. An improvement in electrical conductivity from insulating to conducting with increasing MWCNT content was observed. The carbon nanotube network showed a classical percolating network behavior with a low percolation threshold. Electromagnetic interference (EMI) shielding effectiveness value of about 18 dB was obtained in the frequency range 8.0–12 GHz (X‐band), for a 10 vol% CNT loading. An improved composite fabrication process using casting followed by compression molding and use of functionalized MWCNT resulted in increased composites strength. POLYM. COMPOS., 2008. © 2008 Society of Plastics Engineers     

Thiophene‐based copolymers synthesized by electropolymerization for application as hole transport layer in organic solar cells

Electrically conducting thiophene‐based copolymers were synthesized by electropolymerization. The potential range used has a strong influence on the film structure and properties. The extent of oxidation of the copolymers was determined from the ratio of the oxidation to reduction charge, Q_ox/Q_red. The use of wide potential range leads to reduced films, whereas the narrow range leads to partially oxidized films. The copolymers exhibit a characteristic band in UV–vis spectra at ～ 410 nm, which shifts to higher wavelengths for the more doped material. The electrical conductivity of the copolymers was correlated to their morphology and their structure. The copolymer with higher conductivity is partially reduced, has compact morphology and higher ratio of quinoid to benzenoid rings. The energy gap of the copolymers is reversely proportional to their electrical conductivity. The optical and electrical properties of the copolymers make them very well suited for use as hole transport layers (HTL) in organic opto‐electronic devices. We prepared polymer : fullerene solar cells with copolymer HTLs. The solar cell performance was tested with very encouraging initial results. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

1H NMR,thermal, and conductivity studies on PVAc based gel polymer electrolytes

The lithium‐ion conducting gel polymer electrolytes (GPE), PVAc‐DMF‐LiClO₄ of various compositions have been prepared by solution casting technique. ¹H NMR results reveal the existence of DMF in the gel polymer electrolytes at ambient temperature. Structure and surface morphology characterization have been studied by X‐ray diffraction analysis (XRD) and scanning electron microscopy (SEM) measurements. Thermal and conductivity behavior of polymer‐ and plasticizer‐salt complexes have been studied by differential scanning calorimetry (DSC), TG/DTA, and impedance spectroscopy results. XRD and SEM analyses indicate the amorphous nature of the gel polymer‐salt complex. DSC measurements show a decrease in T_g with the increase in DMF concentrations. The thermal stability of the PVAc : DMF : LiClO₄ gel polymer electrolytes has been found to be in the range of (30–60°C). The dc conductivity of gel polymer electrolytes, obtained from impedance spectra, has been found to vary between 7.6 × 10^?7 and 4.1 × 10^?4 S cm^?1 at 303 K depending on the concentration of DMF (10–20 wt %) in the polymer electrolytes. The temperature dependence of conductivity of the polymer electrolyte complexes appears to obey the VTF behavior. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Uniaxially aligned poly[(9,9‐dioctylfluorenyl‐2,7‐diyl)‐co‐bithiophene] thin films characterized by the X‐ray diffraction pole figure technique

Aligned thin films of the liquid‐crystalline polymer poly[(9,9‐dioctylfluorenyl‐2,7‐diyl)‐co‐bithiophene] were prepared, and the correlation between the optical anisotropy and the structural properties was shown. A series of samples with different thicknesses were prepared via a spin‐casting process on rubbed polyimide surfaces. The alignment of the polymer chains was obtained by a temperature treatment just below the clearing temperature. The degree of alignment was investigated with ultraviolet–visible absorption spectroscopy and in‐plane X‐ray diffraction. Independently, each technique revealed Hermans orientation functions in the range of 0.75–0.8. Surprisingly, a layer‐thickness dependence was not observed. In addition, the X‐ray diffraction pole figure technique revealed that the polymer chains were uniaxially aligned along the rubbing direction. The aligned films were in the nematic state, with the director elongated along the rubbing direction. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Dielectric relaxation and optical properties of polyvinyl chloride/lead monoxide nanocomposites

Sol–gel synthesized lead monoxide (PbO) nanoparticles were mixed with polyvinyl chloride (PVC). The dielectric characteristics of PVC/PbO nancomposite films were studied in the temperature range 303–408 K and frequency range 30 kHz–3 MHz. There is a sharp increase in the dielectric constant (ε′), after the glass transition temperature. According to the temperature and frequency dependence of the dielectric loss modulus (M″), the observed α_a‐relaxation peak is due to the micro‐Brownian motion of the polymer main chains. The behavior of σ_ac (f) for the composite films indicate that the homogenous distribution of PbO nanoparticles allows the formation of conductive three‐dimensional networks throughout the nanocomposite films which assisting the charge carriers to hop from conducting clusters to neighbors. The influences of PbO content on the direct optical band gap and the refractive index of the films are also discussed and compared with those of previous studies of PVC composites. POLYM. COMPOS., 34:2031–2039, 2013. © 2013 Society of Plastics Engineers     

Synthesis and characterization of polyaniline films using Fenton reagent

The chemical oxidation of aniline to form polyaniline (PANI) films and powder samples was made using Fenton reagent as an oxidizing agent in aqueous sulfuric acid medium. The PANI films were monitored by using the quartz crystal microbalance and the electronic absorption techniques. The optimum concentration was determined and the results were justified by measuring the UV–vis absorption spectra for the in situ PANI films. The conductivity for the PANI films and powder samples, prepared in different conditions, was measured. Also, the IR spectra, X‐ray and the thermogravimetric analysis for the PANI powder formed in the bulk were measured and compared with the polymer prepared using ammonium peroxydisulfate. A preliminary investigation to the dielectric properties of the polymer powder was measured and discussed. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Spectroscopic and electrochemical studies on block‐polymer/PMMA blend based composite polymer electrolytes

Poly(methylmethacrylate)(PMMA)/oxymethylene‐linked polyoxyethylene multi‐block polymer(Om‐POE_n, where n represents number of unit  CH₂CH₂O ) blend based composite electrolyte films containing different lithium salt concentration and nanofillers' content are prepared using solvent evaporation technique. The interaction of polymer–salt complex has been confirmed using FTIR spectral studies. The figuration of CPE was studied by XRD. Ionic conductivity and thermal behavior of the CPEs were studied with various salt concentrations, temperature, and nanofillers' content. The surface structure of the CPE is also investigated using scanning electron microscopy. The high room temperature ionic conductivity, transmittivity in the visible region, and thermal stability make these CPEs potential candidates as solid‐like electrolytes for electrochemical devices. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2007     

Synthesis,characterization, and photophysics of a novel conjugated polymer with 1,3,4‐oxadiazole,carbazole, and naphthalene units

A polymer containing 1,3,4‐oxadiazole and carbazole units in the main chain and naphthalene moieties as side groups (P‐OCN) was synthesized by the Wittig reaction of [2,5‐bis(3‐tolylene)1′,3′,4‐oxadiazole]‐9‐(α‐naphthyl)‐carbazole polymer (P‐OCN). The optical properties were investigated with ultraviolet–visible absorption and fluorescence emission spectra. The results showed that the luminescence quantum yield of P‐OCN was 0.673 in chloroform, and it emitted blue and blue‐green light with a band gap of 3.49 eV estimated from the onset absorption. Thermogravimetric analysis and differential scanning calorimetry showed that the polymer exhibited good thermal stability up to 354°C with a glass‐transition temperature higher than 110°C. To investigate the donating and accepting capacities of P‐OCN, the fluorescent quenching technique was used to determinate the interactions between the polymer and the electron donor and electron acceptor. The results showed that the light emission could be quenched by both the electron donor (N,N‐dimethylaniline) and electron acceptor (dimethylterephthalate). Furthermore, the interaction between P‐OCN and fullerene was also studied with fluorescent quenching, and the processes followed the Stern–Volmer equation. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Conducting ferromagnetic copolymer of aniline and 3,4‐ethylenedioxythiophene containing nanocrystalline barium ferrite particles

This article reports the synthesis of conducting ferromagnetic complex of 3,4‐ethylenedioxythiophene (EDOT) and aniline (An) containing M‐type hexagonal barium ferrite (BaFe₁₂O₁₉) particles using in situ emulsion polymerization and electrochemical oxidative polymerization. Magnetic and conductivity studies reveal that the conducting ferromagnetic complex possesses high‐saturation magnetization (M_s) value of 29.2 emu/g and conductivity of the order of 0.256 S/cm determined through vibrating sample magnetometer and four‐probe method. Microwave measurement has shown the reflection loss (R_L) of ?12.1 dB in Ku‐band that can be used as a microwave absorbing material. The polymer complex was further characterized by techniques like X‐ray diffraction, Fourier transform infrared, UV–visible, cyclic voltammetry, and thermal analysis with thermogravimetric analysis. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci 2008     

Investigations on the electrical and structural properties of PVA doped with (NH4)2SO4

Solid polymer electrolytes based on poly(vinyl alcohol) (PVA) complexed with ammonium sulfate (NH₄)₂SO₄ at different weight percent ratios were prepared using solution cast technique. The structural properties of these electrolyte films were examined by X‐ray diffraction (XRD) studies. The XRD data revealed that the amorphous domains of PVA polymer matrix increased with the increase of ammonium sulfate added up to 5 wt %, after which the degree of crystallinity increases. The complexation of the salt with the polymer was confirmed by Fourier transform infrared (FTIR) spectroscopy. Electrical conductivity was measured in the temperature range of 303–373 K. The conductivity was found to obey Arrhenius formula. The dielectric permittivity ε′ was studied as function of temperature and frequency, respectively.The data showed increasing in ε′ values with the increase in temperature while decreased with increase in frequency for polymer electrolyte system up to 10% of ammonium sulfate added. For values of addition greater than 10%, ε′ is independent of both temperature and frequency. The ac conductivity is found to obey the power relation. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Plasma‐polymerized elastomer/conducting polymer composite: Structural and optical characterization

Plasma polymerization is an excellent and inexpensive tool for growing uniform, ultrathin amorphous and pinhole‐free polymer layer on different substrates and also for forming polymer composites. This work reports the synthesis and characterization of Styrene Butadiene Co‐polymer (SBR) based conducting polymer composites by plasma polymerization using a home built DC plasma polymerization setup. Optical, morphological, and cyclic voltammetric studies reveal an effective formation of composite structure containing SBR and Polyaniline (Pani). The chemical structure of the composite film is studied using FTIR spectroscopy. The films prepared are highly cross‐linked, amorphous in nature and have band gap of 2.8 eV. Moreover, it is found that I₂ doping of the composites enhances their conductivity to a desirable value. The band gap energy of the composite film decreases from 2.8 eV to 2 eV by iodine doping. SEM and AFM images show the uniformity in film morphology. The refractive index of the film is found to be 1.87 and dielectric constant is 3.4 at a wavelength 620 nm in the visible region. POLYM. COMPOS., 34:1091–1098, 2013. © 2013 Society of Plastics Engineers