Conducting Polymer Blend Electrolytes Research Articles

Chitosan as a suitable host for sustainable plasticized nanocomposite sodium ion conducting polymer electrolyte in EDLC applications: Structural, ion transport and electrochemical studies

The challenge in front of EDLC device is their low energy density compared to their battery counter parts. In the current study, a green plasticized nanocomposite sodium ion conducting polymer blend electrolytes (PNSPBE) was developed by incorporating plasticized Chitosan (CS) blended with polyvinyl alcohol (PVA), doped with NaBr salt with various concentration of CaTiO3 nanoparticles. The most optimized PNSPBE film was subsequently utilized in an EDLC device to evaluate its effectiveness both as an electrolyte and a separator. Structural and morphological changes were assessed using XRD and SEM techniques. The PNSPBE film demonstrated a peak ionic conductivity of 9.76×10−5 S/cm, as determined through EIS analysis. The dielectric and AC studies provided further confirmation of structural modifications within the sample. Both TNM and LSV analyses affirmed the suitability of the prepared electrolyte for energy device applications, evidenced by its adequate ion transference number and an electrochemical potential window of 2.86 V. Electrochemical properties were assessed via CV and GCD techniques, confirming non-Faradaic ion storage, indicated by the rectangular CV pattern at low scan rates. The parameters associated with the designed EDLC device including specific capacitance, ESR, power density (1950 W/kg) and energy density (12.3 Wh/kg) were determined over 1000 cycles.

The study of ion transport parameters using two models in plasticized sodium ion conducting polymer blend electrolytes

The study of ion transport parameters using two models in plasticized sodium ion conducting polymer blend electrolytes

Dielectric properties and ion transport studies from Trukhan, EIS, and Bandara-Mellander approaches for plasticized sodium ion conducting polymer blend electrolytes

Dielectric properties and ion transport studies from Trukhan, EIS, and Bandara-Mellander approaches for plasticized sodium ion conducting polymer blend electrolytes

Characterization of proton conducting polymer blend electrolyte based on gum tragacanth and polyvinyl alcohol

This paper discusses the development and characterisation of polymer electrolyte films made of gum tragacanth and polyvinyl alcohol that have been doped with ammonium thiocyanate. A minimum amount of PVA was added to improve mechanical stability. Free-standing films were obtained with different salt ratios through the solution casting technique. Physical characterisation methods such as X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FTIR) were used to investigate the structural characteristics and the interactions between the polymer and the salt. Electrochemical impedance spectroscopy was used to examine the produced membranes' electrical characteristics (EIS). The blend polymer complexes' dc conductivity was observed to rise with salt content, reaching a maximum of 5.61 × 10-3 Scm−1 at ambient temperature. The system GT-ATC was discovered to exhibit Arrhenius behaviour in its temperature dependency. The non-Debye character of the electrolytes was apparent in the dielectric spectra.

Microstructure and electrical properties of Li+ ion conducting polymer blend electrolyte films

Microstructure and electrical properties of Li+ ion conducting polymer blend electrolyte films

Synthesis of Solid Polymer Blend Electrolytes Based on PVP/PAN/Ammonium Thiocyanate: Structural, Electrical, Dielectric and Electrochemical Analysis

In this work, a solution casting technique was used to prepare stable and free-standing films of blend polymer electrolytes composed of polyvinyl pyrrolidone (PVP) and polyacrylonitrile (PAN) complexed with ammonium thiocyanate (NH4SCN) salt in various compositions. The physical characterization by X-ray diffraction (XRD) was performed to study the structural properties of the samples. Characteristics of these electrolytes were also examined using impedance technique, dielectric studies, transport number measurement (TNM) and linear sweep voltammetry (LSV). The results showed that cationic transport predominated in highly amorphous films. Impedance spectroscopy was utilized to determine the dependence of electrical properties on both composition and temperature. The temperature dependence of the electrical conductivity showed behaviour similar to that of Arrhenius type. It was found that the highest ion conducting polymer blend electrolyte led to lower activation energy.

Proton conducting polymer blend electrolytes based on MC: FTIR, ion transport and electrochemical studies

In this work, the free-standing plasticized solid polymer electrolyte films were made utilizing methylcellulose (MC) and dextran (DN) doped with ammonium fluoride (NH 4 F) and plasticized with glycerol by a typical solution casting approach. Based on the characterizations, MC-DN-NH 4 F electrolyte has been shown to improve the structural, electrical, and electrochemical properties resulting from the dispersion of glycerol plasticizer. The electrochemical impedance spectroscopy (EIS) measurement for the highest inclusion of plasticizer revealed a conductivity of 2.25 × 10 -3 S/cm. The electrical equivalent circuit (EEC) model has established the circuit elements for each electrolyte. The variation trend of dielectric constant and DC conductivity was matched and confirmed by the EIS data. The fourier transform infrared (FTIR) analysis displayed credible confirmation of polymers-ion-plasticizer interactions. The dielectric study is extra highlighted the conductivity behavior. The dielectric constant and loss (ε′ and ε″) quantities were reported to be high at low frequencies. On the other hand, the irregular shape of the imaginary part of modulus (M“) spectra denotes the non-Debye behaviors of relaxation. The ion transference number (t ion ) value for the maximum plasticized system is 0.944, where the ions are the primary components for the charge transfer process. Stability of the highest conducting sample is determined to be 1.6 V, using linear sweep voltammetry (LSV).

Polysiloxane‐Based Single‐Ion Conducting Polymer Blend Electrolyte Comprising Small‐Molecule Organic Carbonates for High‐Energy and High‐Power Lithium‐Metal Batteries

AbstractSingle‐ion conducting polymer electrolytes are considered particularly attractive for realizing high‐performance solid‐state lithium‐metal batteries. Herein, a polysiloxane‐based single‐ion conductor (PSiO) is investigated. The synthesis is performed via a simple thiol‐ene reaction, yielding flexible and self‐standing polymer electrolyte membranes (PSiOM) when blended with poly(vinylidene fluoride‐co‐hexafluoropropylene) (PVdF‐HFP). When incorporating 57 wt% of organic carbonates, these polymer membranes provide a Li+ conductivity of >0.4 mS cm−1 at 20 °C and a wide electrochemical stability window of more than 4.8 V. This excellent electrochemical stability allows for the highly reversible cycling of symmetric Li||Li cells as well as high‐energy Li||LiNi0.6Mn0.2Co0.2O2 (NMC622) and Li||LiNi0.8Mn0.1Co0.1O2 (NMC811) cells for several hundred cycles at relatively high discharge and charge rates. Remarkably, Li||NMC811 cells with high mass loading cathodes provide more than 76% capacity retention at a high current density of 1.44 mA cm−2, thus rendering this polymer electrolyte suitable for high‐performance battery applications.

Development of Flexible Plasticized Ion Conducting Polymer Blend Electrolytes Based on Polyvinyl Alcohol (PVA): Chitosan (CS) with High Ion Transport Parameters Close to Gel Based Electrolytes.

In the current study, flexible films of polyvinyl alcohol (PVA): chitosan (CS) solid polymer blend electrolytes (PBEs) with high ion transport property close enough to gel based electrolytes were prepared with the aid of casting methodology. Glycerol (GL) as a plasticizer and sodium bromide (NaBr) as an ionic source provider are added to PBEs. The flexible films have been examined for their structural and electrical properties. The GL content changed the brittle and solid behavior of the films to a soft manner. X-ray diffraction (XRD) and Fourier transform infrared (FTIR) methods were used to examine the structural behavior of the electrolyte films. X-ray diffraction investigation revealed that the crystalline character of PVA:CS:NaBr declined with increasing GL concentration. The FTIR investigation hypothesized the interaction between polymer mix salt systems and added plasticizer. Infrared (FTIR) band shifts and fluctuations in intensity have been found. The ion transport characteristics such as mobility, carrier density, and diffusion were successfully calculated using the experimental impedance data that had been fitted with EEC components and dielectric parameters. CS:PVA at ambient temperature has the highest ionic conductivity of 3.8 × 10 S/cm for 35 wt.% of NaBr loaded with 55 wt.% of GL. The high ionic conductivity and improved transport properties revealed the suitableness of the films for energy storage device applications. The dielectric constant and dielectric loss were higher at lower frequencies. The relaxation nature of the samples was investigated using loss tangent and electric modulus plots. The peak detected in the spectra of tanδ and M” plots and the distribution of data points are asymmetric besides the peak positions. The movements of ions are not free from the polymer chain dynamics due to viscoelastic relaxation being dominant. The distorted arcs in the Argand plot have confirmed the viscoelastic relaxation in all the prepared films.

Preparation and characterization of proton conducting polymer blend electrolytes (PVC/PMMA/NH4SCN)

Preparation and characterization of proton conducting polymer blend electrolytes (PVC/PMMA/NH4SCN)

Promising biodegradable polymer blend electrolytes based on cornstarch:PVP for electrochemical cell applications

Higher proton conducting polymer blend electrolytes (HPCPBEs) of cornstarch:poly vinyl pyrrolidone (PVP):ammonium thiocyanate (NH4SCN) have been prepared by solution casting technique. Enhancement of amorphous nature of the polymer blend electrolytes have confirmed by X-ray diffraction analysis. The presence of functional groups in Fourier transform infrared spectrum shows the complexation between salt and host polymer matrix. At ambient temperature, 70 wt% NH4SCN mixed composition has obtained the maximum conductivity (1.36 × 10–4 S cm–1). The dielectric properties of the prepared samples have been analysed. The dielectric spectra and modulus spectra reveal the non-Debye behaviour of the polymer electrolytes. Low activation energy (0.14 eV) with regression value of 0.98 has been revealed from temperature dependence of ionic conductivity studies. Wagner’s polarization technique is used to confirm the conductivity due to the ions. Electrochemical behaviour of HPCPBE has been analysed by cyclic voltammetry. An electrochemical cell has fabricated using the HPCPBE and the observed open circuit voltage is 1.15 V.

The Study of Plasticized Sodium Ion Conducting Polymer Blend Electrolyte Membranes Based on Chitosan/Dextran Biopolymers: Ion Transport, Structural, Morphological and Potential Stability.

The polymer electrolyte system of chitosan/dextran-NaTf with various glycerol concentrations is prepared in this study. The electrical impedance spectroscopy (EIS) study shows that the addition of glycerol increases the ionic conductivity of the electrolyte at room temperature. The highest conducting plasticized electrolyte shows the maximum DC ionic conductivity of 6.10 × 10−5 S/cm. Field emission scanning electron microscopy (FESEM) is used to investigate the effect of plasticizer on film morphology. The interaction between the electrolyte components is confirmed from the existence of the O–H, C–H, carboxamide, and amine groups. The XRD study is used to determine the degree of crystallinity. The transport parameters of number density (n), ionic mobility (µ), and diffusion coefficient (D) of ions are determined using the percentage of free ions, due to the asymmetric vibration (υas(SO3)) and symmetric vibration (υs(SO3)) bands. The dielectric property and relaxation time are proved the non-Debye behavior of the electrolyte system. This behavior model is further verified by the existence of the incomplete semicircle arc from the Argand plot. Transference numbers of ion (tion) and electron (te) for the highest conducting plasticized electrolyte are identified to be 0.988 and 0.012, respectively, confirming that the ions are the dominant charge carriers. The tion value are used to further examine the contribution of ions in the values of the diffusion coefficient and mobility of ions. Linear sweep voltammetry (LSV) shows the potential window for the electrolyte is 2.55 V, indicating it to be a promising electrolyte for application in electrochemical energy storage devices.

The Study of Structural, Impedance and Energy Storage Behavior of Plasticized PVA:MC Based Proton Conducting Polymer Blend Electrolytes.

In this study, structural characterization, electrical properties and energy storage performance of plasticized polymer electrolytes based on polyvinyl alcohol/methylcellulose/ammonium thiocyanate (PVA/MC-NH4SCN) were carried out. An X-ray diffraction (XRD) study displayed that the plasticized electrolyte system with the uppermost value of direct current (DC) ionic conductivity was the most amorphous system. The electrolyte in the present work realized an ionic conductivity of 2.903 × 10−3 Scm−1 at room temperature. The main charge carrier in the electrolyte was found to be the ions with the ionic transference number (tion) of 0.912, compared to only 0.088 for the electronic transference number (telec). The electrochemical stability potential window of the electrolyte is 2.1 V. The specific capacitance was found to reduce from 102.88 F/g to 28.58 F/g as the scan rate increased in cyclic voltammetry (CV) analysis. The fabricated electrochemical double layer capacitor (EDLC) was stable up to 200 cycles with high efficiency. The specific capacitance obtained for the EDLC by using charge–discharge analysis was 132.7 F/g at the first cycle, which is slightly higher compared to the CV plot. The equivalent series resistance (ESR) increased from 58 to 171 throughout the cycles, which indicates a good electrolyte/electrode contact. Ions in the electrolyte were considered to have almost the same amount of energy during the conduction process as the energy density is approximately at 14.0 Wh/kg throughout the 200 cycles. The power density is stabilized at the range of 1444.3 to 467.6 W/kg as the EDLC completed the cycles.

Proton conducting polymer electrolyte based on cornstarch, PVP, and NH4Br for energy storage applications

Proton conducting polymer blend electrolytes based on cornstarch and polyvinyl pyrrolidone (PVP) with ammonium bromide (NH4Br) were prepared by the technique of solution casting. Enhancement of amorphous nature by the addition of NH4Br has confirmed by XRD. In FTIR,by the addition of NH4Br salt in the optimized blend system, there occurs a change like altering the peak intensity, peak shape, and position. This reveals the appearance of complex formation between the polymer and salt. At 358 K, 30 wt.% of NH4Br added system shows the maximum conductivity (1.31 × 10−4 S cm−1). The conduction mechanism of higher conducting polymer blend electrolytes follows the quantum mechanical tunneling (QMT) at mid-frequency and overlapping large polaron tunneling (OLPT) at higher frequency. High dielectric constant and low relaxation time of ions in polymer chain are obtained for 30 wt.% of NH4Br added polymer blend electrolyte. From Wagner’s polarization technique, it is established that conduction present in the polymer electrolytes is predominately due to ions. Faradaic pseudo capacity behaviour has observed in higher conducting sample by cyclic voltammetry. The electrochemical cell has prepared by the higher conducting polymer electrolyte and the open circuit potential (OCP) of 1.24 V has achieved from prepared electrochemical cell.

Synthesis of Porous Proton Ion Conducting Solid Polymer Blend Electrolytes Based on PVA: CS Polymers: Structural, Morphological and Electrochemical Properties.

In this study, porous cationic hydrogen (H+) conducting polymer blend electrolytes with an amorphous structure were prepared using a casting technique. Poly(vinyl alcohol) (PVA), chitosan (CS), and NH4SCN were used as raw materials. The peak broadening and drop in intensity of the X-ray diffraction (XRD) pattern of the electrolyte systems established the growth of the amorphous phase. The porous structure is associated with the amorphous nature, which was visualized through the field-emission scanning electron microscope (FESEM) images. The enhancement of DC ionic conductivity with increasing salt content was observed up to 40 wt.% of the added salt. The dielectric and electric modulus results were helpful in understanding the ionic conductivity behavior. The transfer number measurement (TNM) technique was used to determine the ion (tion) and electron (telec) transference numbers. The high electrochemical stability up to 2.25 V was recorded using the linear sweep voltammetry (LSV) technique.

The Study of Electrical and Electrochemical Properties of Magnesium Ion Conducting CS: PVA Based Polymer Blend Electrolytes: Role of Lattice Energy of Magnesium Salts on EDLC Performance.

Plasticized magnesium ion conducting polymer blend electrolytes based on chitosan (CS): polyvinyl alcohol (PVA) was synthesized with a casting technique. The source of ions is magnesium triflate Mg(CF3SO3)2, and glycerol was used as a plasticizer. The electrical and electrochemical characteristics were examined. The outcome from X-ray diffraction (XRD) examination illustrates that the electrolyte with highest conductivity exhibits the minimum degree of crystallinity. The study of the dielectric relaxation has shown that the peak appearance obeys the non-Debye type of relaxation process. An enhancement in conductivity of ions of the electrolyte system was achieved by insertion of glycerol. The total conductivity is essentially ascribed to ions instead of electrons. The maximum DC ionic conductivity was measured to be 1.016 × 10−5 S cm−1 when 42 wt.% of plasticizer was added. Potential stability of the highest conducting electrolyte was found to be 2.4 V. The cyclic voltammetry (CV) response shows the behavior of the capacitor is non-Faradaic where no redox peaks appear. The shape of the CV response and EDLC specific capacitance are influenced by the scan rate. The specific capacitance values were 7.41 F/g and 32.69 F/g at 100 mV/s and 10 mV/s, respectively. Finally, the electrolyte with maximum conductivity value is obtained and used as electrodes separator in the electrochemical double-layer capacitor (EDLC) applications. The role of lattice energy of magnesium salts in energy storage performance is discussed in detail.

Structural, electrical and electrochemical studies of sodium ion conducting blend polymer electrolytes

In the present study sodium ion conducting polymer blend electrolytes has been prepared using poly (vinylidene fluoride – hexafluoro – propylene) (PVdF-HFP), poly (methyl methacrylate) (PMMA), and sodium thiocyanate (NaSCN) salt by solution-cast technique. The highest ionic conductivity of the optimized blend polymer electrolyte system [PVdF(HFP)-PMMA (4:1)] (20 wt%)-[NaSCN (1 M)] (80 wt%) has been found to be 4.54 × 10−2 S cm−1 at room temperature. The temperature dependence conductivity plot shows the Arrhenius behaviour and its activation energy calculated from the plot were found to be 0.13 eV. The structural and morphological studies of polymer blend electrolyte were investigated by XRD, SEM and FTIR spectroscopy. Complex formation between polymer and salt has been confirmed by these studies. The thermal properties of optimized electrolyte system were examined by differential scanning calorimetry (DSC) techniques. The ionic transport number was calculated using d.c polarization techniques and was found to be 0.92, which shows that electrolyte system is predominantly ionic in nature. The electrochemical potential window of optimized polymer blend electrolyte was tested and observed to be ∼2.8 V.

Investigations of lithium ion conducting polymer blend electrolytes using biodegradable cornstarch and PVP

Solid polymer electrolytes used in energy storage devices based on Cornstarch and Poly (vinyl Pyrrolidone) blend incorporated with lithium acetate was prepared using the solution casting method. XRD results confirmed that the amorphous nature of the as-prepared polymer electrolyte was increased by addition of salt. 80 wt % Cornstarch/20 wt % PVP/60 wt % lithium acetate added polymer blend system attains better amorphous nature than others. At ambient temperature, 60 wt % of lithium acetate added system has better bulk conductivity of 3.52 × 10−5Scm−1 over the frequency range of 42 Hz to 1 MHz using AC impedance spectroscopy studies. The dielectric analysis is confirmed that the higher conducting sample was having high dielectric constant and low relaxation time for enhancing ions dynamic behaviour. The conduction mechanism of the higher conducting polymer electrolyte is explained by small polaron hopping and overlapping large polaron tunnelling conduction mechanism. From the argand plot, it is confirmed that higher conducting sample has low relaxation time.

High Proton Conducting Polymer Blend Electrolytes Based on Chitosan:Dextran with Constant Specific Capacitance and Energy Density.

Polymer blend electrolytes based on chitosan: dextran (CS:Dext) incorporated with various amounts of ammonium fluoride (NH4F) with constant specific capacitance (12.4 F/g) and energy density over 100 cycles were prepared using a solution cast technique. The blend electrolyte samples exhibit broader amorphous humps in X-ray diffraction (XRD) spectra compared to pure CS:Dext film. The Fourier transform infrared (FTIR) study indicates the complex formation of the added ammonium salt with the polymer blend functional groups through the shifting and decrease in the intensity of FTIR bands. The impedance plots were used to determine the conductivity of the samples. The field emission scanning electron microscopy (FESEM) images support the conductivity behavior of the samples. The impedance plots were applied in the determination of the conductivity of the samples in which the relatively highest conductivity was gained to be 1 × 10−3 S/cm. The transference number measurement (TNM) of the conducting electrolyte was 0.88, which portrays the dominancy of ion in the conduction process. Linear sweep voltammetry (LSV) verified the chemical stability and showed it to be 1.7 V and an effective electrical double layer capacitor (EDLC) that is applicable in electrochemical devices. The performance of the EDLC cell was examined using both cyclic voltammetry and constant current charge–discharge techniques at ambient temperature. The semi-rectangular shape of the cyclic voltammetry (CV) plot and no redox peak was observed. The charge-discharge process of the fabricated EDLC is durable over 100 cycles with an equivalent circuit resistance and power density of 194.5 Ω and 428 W/kg, respectively. Two main outcomes, the specific capacitance and energy densities of 12.4 Farad/g and 1.4 Wh/kg, respectively, are almost constant over 100 cycles.

Influence of 1-ethyl-3-methylimidazolium bis (trifluoromethyl sulfonyl) imide plasticization on zinc-ion conducting PEO/PVdF blend gel polymer electrolyte

The influence in terms of plasticizer on zinc-ion conducting polymer blend electrolyte system, [PEO (90 wt%)/PVdF (10 wt%)]-15 wt% Zn (CF3SO3)2] with various concentrations of 1-ethyl-3-methylimidazolium bis (trifluoromethylsulfonyl) imide (EMIMTFSI) was investigated. The freshly-prepared thin films of [PEO (90 wt%)/PVdF (10 wt%)]-15 wt% Zn (CF3SO3)2) + x wt% EMIMTFSI, where x = 1, 3, 5, 7, and 10 wt%] were characterized by means of X-ray diffraction (XRD), Fourier transformed infrared (FTIR), scanning electron microscopy (SEM), differential scanning calorimetry (DSC) and impedance analysis techniques. The room temperature XRD patterns tend to support the enhanced amorphous phase as a result of deducing the degree of crystallinity of the polymer blend–salt system by the addition of 7 wt% EMIMTFSI. The relevant SEM images of 7 wt% EMIMTFSI incorporated gel polymer electrolyte exhibit a minimised spheurilite structure when compared to that of the polymer blend–salt system. Unusually, the highest ionic conductivity realized in the case of the typical gel polymer electrolyte system, [PEO/PVdF-Zn (CF3SO3)2 + 7 wt% EMIMTFSI] is found to be 1.63 × 10−4 S cm−1 at room temperature. The temperature dependence of conductivity has been examined based on the Vogel–Tammann–Fulcher (VTF) equation, thereby suggesting the segmental chain motion and free volume changes. The occurrence of ion dynamics and dielectric relaxation behaviour in the chosen system has been analysed in a detailed fashion at room temperature using frequency response impedance formalisms involving electric modulus and dielectric permittivity features.