Fabrication and Characterization of Flexible Solid Polymers Electrolytes for Supercapacitor Application

In this work, solid flexible polymer blend electrolytes (PBE) composed of polyvinyl alcohol (PVA) and polyvinyl pyrrolidone (PVP) with different amounts of sodium thiocyanate (NaSCN) salt mixed in double-distilled water (solvent) are prepared via solution casting method. The obtained films are characterized using several techniques. The study of the surface morphology of the polymer blend salt complex films via the POM technique reveals the presence of amorphous regions due to the NaSCN effect. FTIR spectra studies confirm the complex formation between PVA, PVP, and NaSCN. The addition of 20 wt% NaSCN salt in the composition PVA: PVP (50:50 wt%) polymer blend matrix leads to an increase in the number of charge carriers and thus improves the ionic conductivity. The ionic conductivity of each polymer blend electrolyte was studied using the electrochemical impedance spectroscopy (EIS) method. The highest room temperature ionic conductivity of 8.1 × 10−5 S/cm S cm−1 is obtained for the composition of PVA: PVP (50:50 wt%) with 20 wt% NaSCN. LSV test shows the optimized ion-conducting polymer blend electrolyte is electrochemically stable up to 1.5 V. TNM analysis reveals that 99% of ions contribute for the conductivity against 1% of electrons only in the highly conductive polymer electrolyte PVA: PVP (50:50 wt%) + 20 wt% NaSCN. A supercapacitor device was fabricated using the optimized ion-conducting polymer blend film and graphene oxide (GO) coated electrodes. The GCD curve clearly reveals the behavior of an ideal capacitor with less Faradic process and low ESR value. The columbic efficiency of the GO-based system is found to be 100%, the GO-based electrode exhibits a specific capacitance of 12.15 F/g and the system delivers the charge for a long duration. The specific capacitance of the solid-state supercapacitor cell was found to be 13.28 F/g via the CV approach close to 14.25 F/g obtained with EIS data at low frequency.


Introduction
Solid polymer salt complexes are having great worth in diverse electrochemical devices such as fuel cells, supercapacitors, high-energy batteries, display devices, gas sensors, etc., [1][2][3][4]. Because of their excellent interface contact between the electrode and electrolyte, large range of content, and the facilitation of preparation, polymers are highly preferred over crystalline materials. Particularly, polyvinyl alcohol (PVA) is a promising polymer pure PVC-based PE (10 −7 S cm −1 ). Irfan et al. [21] developed SPE based on PVA and PVP doped with sodium fluoride (NaF). The salt incorporation into the polymer blend led to a reduced degree of crystallinity and thus increases its conductivity. The electrolyte system showed a predominance of ionic charges upon electrons and the optical properties of the electrolyte films relied on the content of NaF salt. New solid polymer blend electrolytes were fabricated by Deshmukh et al. [22] using PVA and PVP mixed with various weight percentages of lithium carbonate (Li 2 CO 3 ) salt via solution casting technique. As a result, the conductivity has increased with the variation of salt concentration and its maximum value was about 1.15 × 10 −5 S cm −1 for 20 wt% Li 2 CO 3 and also showed a strong dielectric dispersion due to the Li 2 CO 3 concentration increase. PVA/PVP/ Li 2 CO 3 systems seemed auspicious for solid-state batteries. Mohd and his colleagues [23] prepared ion conducting blend PEs based on PVA/PVP with sodium bicarbonate (NaHCO3). The polymer blend electrolytes showed a reduced degree of crystallinity due to an increase in NaHCO 3 concentration. The obtained films were free-standing with good flexibility and exhibited good mechanical properties. The blend of PVA and PVP expects to create an interchain hydrogen connection between the hydroxyl group of PVA and the carbonyl group of PVP [24].
By dissolving inorganic salt in the host lattice, high conductivity and stabilized electrochemical properties are to be obtained from the mixture of PEs. In this work, PVA with its good mechanical properties is mixed with PVP and NaSCN for film preparation. Solid ion-polymer blend electrolytes are developed with different salt contents for supercapacitor device fabrication.

Materials and Methods
Polyvinyl alcohol (PVA) (Mw 89,000-98,000 g mol −1 ) and polyvinyl propylene (PVP) (Mw: 40,000 g mol −1 ) are used both as host polymers to develop new flexible solid polymer blend electrolytes. Sodium thiocyanate (NaSCN) (Mw: 81.07 g mol −1 ) was utilized as an ion supplier and double-distilled water (DDW) as solvent. All the products were bought from Sigma-Aldrich, Bengaluru (India). The samples were characterized using the Motic (BA 310 model, California, USA) for carrying out the POM method, Perkin-Elmer FTIR spectrometer (model RX1) was used for FTIR measurements, and CH instruments CHI660D (Model 600 series electrochemical analyzer/workstation, USA) was used for EIS measurements.

Polymer Blend Synthesis without Salt
Solid polymer blend electrolyte films were prepared using the solution casting method. An equal amount of 50 wt% PVA and 50 wt% PVP (wt% = weight percentage) are dissolved in DDW separately and placed on a magnetic stirrer for about 4 h. Both solutions were then mixed and stirred for more than 4 h.

Polymer Blend Synthesis with Salt
The blend solution (PVA-PVP) is then doped with the dissolved solutions of NaSCN with x concentrations (x = 5, 10, 15, 20, 25 wt%). The different mixtures were stirred for 6 h at 50 • C till homogeneous solutions are obtained for each NaSCN composition. All the solutions are poured into Petri dishes at room temperature and placed in a desiccator containing powder silica gels for 2 weeks to remove all the solvent molecules before characterization. After desiccation, solid flexible polymer blend electrolyte films obtained were transparent and were further investigated. The optimized sample is then used for the supercapacitor device as explained in the following sections.

Measurements
All the prepared films of pure PVA, pure PVP, blend PVA/PVP, and PVA/PVP: NaSCN electrolyte samples with different salt content were analyzed via several approaches. The electrochemical characterizations such as EIS, LSV, TNM, and CV analysis are performed using the electrochemical workstation CH-instrument (USA model) over the frequency range 1-0.05 MHz.

Polarized Optical Microscopy (POM)
The surface morphology of the samples was explored using optical microscopy by Motic (BA 310 model, California, USA) to check the impact of the NaSCN in the PVA: PVP blend.

Fourier Transform Infrared Spectroscopy (FTIR)
The different polymer-ion interactions and specific functional groups present in polymer blend electrolyte samples are determined over the range of 4000-650 cm −1 at room temperature using a Perkin-Elmer FTIR spectrometer (model RX1). This technique is also performed to check the complexation between PVA, PVP, and NaSCN.

Electrochemical Impedance Spectroscopy (EIS)
The electrochemical behavior of each sample was studied using the EIS approach which depends on AC potentials frequency. The EIS method is also used to measure the electrical resistance (impedance) between the PE/electrode. This resistance value depends upon the addition of different amounts of NaSCN to the PVA: PVP blend.

Conductivity Measurements
The conductivity (σ) was measured by sandwiching each PE film between two stainless steel electrodes using a sample holder as shown in Figure 1. The conductivity was calculated using the standard formula [25]: where R b is the bulk resistance, A is the section-area (1 × 1 cm 2 ) of the film, and t is the thickness of the sample measured with a screw gauge 0-25 mm.
percapacitor device as explained in the following sections.

Measurements
All the prepared films of pure PVA, pure PVP, blend PVA/PVP, and PVA/PVP: NaSCN electrolyte samples with different salt content were analyzed via several approaches. The electrochemical characterizations such as EIS, LSV, TNM, and CV analysis are performed using the electrochemical workstation CH-instrument (USA model) over the frequency range 1 MHz-0.05 mHz.

Polarized Optical Microscopy (POM)
The surface morphology of the samples was explored using optical microscopy by Motic (BA 310 model, California, USA) to check the impact of the NaSCN in the PVA: PVP blend.

Fourier Transform Infrared Spectroscopy (FTIR)
The different polymer-ion interactions and specific functional groups present in polymer blend electrolyte samples are determined over the range of 4000-650 cm −1 at room temperature using a Perkin-Elmer FTIR spectrometer (model RX1). This technique is also performed to check the complexation between PVA, PVP, and NaSCN.

Electrochemical Impedance Spectroscopy (EIS)
The electrochemical behavior of each sample was studied using the EIS approach which depends on AC potentials frequency. The EIS method is also used to measure the electrical resistance (impedance) between the PE/electrode. This resistance value depends upon the addition of different amounts of NaSCN to the PVA: PVP blend.

Conductivity Measurements
The conductivity ( ) was measured by sandwiching each PE film between two stainless steel electrodes using a sample holder as shown in Figure 1. The conductivity was calculated using the standard formula [25]: where is the bulk resistance, is the section-area (1 × 1 cm 2 ) of the film, and is the thickness of the sample measured with a screw gauge 0-25 mm.

Dielectric Constant
Dielectric constant (ε * ) was measured for each sample using Equation (2): The dielectric constant values are calculated from the complex impedance data at 1 kHz frequency.
The real part of the complex permittivity (ε ) is obtained from Equation (3): where Z and Z are real and imaginary part of impedance spectroscopy (Z * ), ω is the angular frequency (ω = 2π f ), C 0 = ε 0 A d is the capacitance of free space and ε 0 permittivity of free space.

Carrier Concentration and Mobility
Carrier concentration (n 0 ) and mobility (µ) can be determined using Equations (4) and (5) respectively [26]: where σ 0 is quasi dc conductivity, e elementary charge, K and T are Boltzmann constant and thermodynamic temperature respectively, and the effective dielectric constant is expressed as [26] ε (ω 10ε ) = 10ε s . The mobility is then calculated using the following Equation (5) [26]:

Linear Speed Voltammetry (LSV)
This approach was carried out to check the breakdown voltage of the optimized polymer blend electrolyte. The working electrode's current can also be measured using the LSV method as the potential difference between it and a reference electrode is linearly changed over time.

Transference Number Measurements (TNM)
Wagner's polarization technique is used to evaluate the ionic and electronic contribution of the conductivity. A fixed voltage is given to the sample at a fixed scan rate and the current density is measured over a range of time. The contribution is evaluated by calculating both ion transference number (t ion ) and electronic transference number (t elec ) using the following expressions: where I ss and I t are the steady state and total currents, respectively.

Synthesis of Electrode Material
Graphene oxide (GO) as electrode material was developed via the exfoliation method [27]. A solution was prepared by mixing H 2 SO 4 with DDW in the ratio of 10:90 wt%. Platinum cable and graphite bar are connected with electric wires initially linked to a power supply and then placed in the prepared solution. The entire system was protected with a paraffin membrane and received a constant voltage of 4 V that was applied for 5 h to finalize the exfoliation process. The dark solution obtained was entirely ultrasonicated, cleaned, purified, desiccated, and collected. The final product was then placed in the oven at 80 • C. The highly conductive polymer blend electrolyte and two identical electrodes were used to make the supercapacitor device. The electrodes were prepared using two clean graphite sheets with an area of 1 × 1 cm 2 as current collectors and doped with an active material (GO). The active material was prepared by dissolving P (VDF-HFP) used as a binder in a small quantity of acetone (solvent) and mixed with GO in a proportion of 10:90 wt% and crushed to form a paste. The graphite sheets were then uniformly coated with the GO paste and further dried in the oven at 80 • C for the whole night.

Supercapacitor Device Assembly
Finally, the optimized flexible solid electrolyte was embedded between two identical electrodes to manufacture a supercapacitor. The different components of the supercapacitor device were assembled as shown in Figure 2.
The highly conductive polymer blend electrolyte and two identical electrodes were used to make the supercapacitor device. The electrodes were prepared using two clean graphite sheets with an area of 1 × 1 cm 2 as current collectors and doped with an active material (GO). The active material was prepared by dissolving P (VDF-HFP) used as a binder in a small quantity of acetone (solvent) and mixed with GO in a proportion of 10:90 wt% and crushed to form a paste. The graphite sheets were then uniformly coated with the GO paste and further dried in the oven at 80 °C for the whole night.

Supercapacitor Device Assembly
Finally, the optimized flexible solid electrolyte was embedded between two identical electrodes to manufacture a supercapacitor. The different components of the supercapacitor device were assembled as shown in Figure 2.

Characterization of the Supercapacitor Device
Cyclic Voltammetry This approach is used to check the electrochemical behavior of the supercapacitor cell at the electrolyte-electrode interface and its performance over a fixed voltage range. The specific capacitance ( ) value of the supercapacitor device is calculated from the graph using the following expression: where is the average current, is the scan rate, and is the capacitance of one electrode, and m is the mass of the electrode material.

Galvanostatic Charge-Discharge (GCV)
This experiment is experimentally opposite to cyclic voltammetry where the supercapacitor charges and discharges within a range of voltage at a constant applied current. This method reflects the real-world performance of the device. The coulombic efficiency was calculated by using the Equation (9): where indicates the discharging time and the charging time.

Characterization of the Supercapacitor Device Cyclic Voltammetry
This approach is used to check the electrochemical behavior of the supercapacitor cell at the electrolyte-electrode interface and its performance over a fixed voltage range. The specific capacitance (C sp ) value of the supercapacitor device is calculated from the graph using the following expression: where i is the average current, s is the scan rate, and C is the capacitance of one electrode, and m is the mass of the electrode material.

Galvanostatic Charge-Discharge (GCV)
This experiment is experimentally opposite to cyclic voltammetry where the supercapacitor charges and discharges within a range of voltage at a constant applied current. This method reflects the real-world performance of the device. The coulombic efficiency was calculated by using the Equation (9): where ∆t D indicates the discharging time and ∆t C the charging time.
The specific capacitance of the device was also calculated from the galvanostatic charge/discharge using the Equation (10): where I is the discharge current, dV/dt is the slope of the discharge curve, and m is the mass of the electrode material.

Low Frequency-Impedance Spectroscopy (IS)
This method is used to measure the specific capacitance at low frequency. The specific capacitance exhibited by the supercapacitor device is then calculated as follows (11): where Z is the low-frequency imaginary part of impedance, m is the active electrode material and f is the frequency.

Surface Morphology Investigations of Polymer Blend Electrolyte films (POM Analysis)
The surface morphologies of pristine PVA, pristine PVP, NaSCN, polymer blend PVA-PVP film, and the optimized PVA-PVP: NaSCN PE samples were recorded and studied ( Figure 3). The micrographs of the prepared films appeared to be almost homogeneous and uniform. The surface morphology of pristine PVA film ( Figure 3a) and PVP film (Figure 3b) have both a uniform surface morphology with a rather smooth surface. In addition, no features are attributed to a crystalline morphology. Figure 3c shows the NaSCN sample used as a dopant to make a complex system with the polymer blend PVA/PVP. The surface morphology of the pure polymer blend PVA-PVP film and the optimized PVA-PVP: NaSCN film are shown in Figure 3d,e respectively. Both micrographs of polymer blend PVA/PVP films show the degree of homogeneity due to the impact of salt distribution through the blend matrix. The morphology surface of the pure PVA-PVP blend matrix looks uniform and also PVA and PVP are completely miscible. The surface morphology of the pure polymer blend reveals the presence of interconnected micropores. The porosity of the structure is related to the high degree of porosity of PVA which enables adsorption of a large quantity of water while its network structure remains unchanged. PVA can be used as highly porous hydrogels because of the network architecture of interconnected polymer chains that drives molecular diffusion [29]. The porous interconnected structure not only promotes the diffusion of molecules and ions as well within the matrix but also plays the role of filter for the pure PVA-PVP blend which only allows molecules and ions with sizes lesser than the pore size. However, the highly interconnected porous structure of the PVA-PVP blend is favorable for ion transport due to the increase of the O-H and C=O bonds and the amorphous structure of PVP which acts as a plasticizer in the system to enhance the conductivity of the membrane. It is observed that the addition of 20 wt% NaSCN to pure polymer blend has changed the surface morphology due to the salt distribution through the matrix. It can be noticed that the pore size was shrunk due to the penetration of the NaSCN in the cross-linked blend structure ( Figure 3e). This reduction in pore size may be related to the salt penetration which promotes better conductivity of Na + . However, the crystalline phase remains in the polymer blend matrix.

FTIR Analysis
The complex formation between the PVA-PVP polymer blend and the NaSCN salt was investigated by FTIR spectroscopy. Figure 4 shows the IR spectra of salt, polymer blend, and the optimized polymer blend electrolyte. Figure 4(a) reveals the IR spectrum of NaSCN. Some vibration peaks can be clearly observed: at 2821, 2072, 1760, 1438, 1406,

FTIR Analysis
The complex formation between the PVA-PVP polymer blend and the NaSCN salt was investigated by FTIR spectroscopy. Figure 4 shows the IR spectra of salt, polymer blend, and the optimized polymer blend electrolyte. Figure

AC Impedance Analysis
The electrical behavior of the solid flexible polymer blend electrolytes was investigated via the AC impedance method. Figure 5 shows the Nyquist plots of pure PVA-PVP and PVA-PVP-NaSCN polymer blend electrolytes with different concentrations (5, 10, 15, 20, 25%wt NaSCN) at room temperature. The graph shows a semicircle in the high-frequency region and a spike in the low-frequency region. The presence of the semi-circle is due to the volume effect of the electrolyte and the spike is caused by the blocking effect of the electrodes [30]. The bulk electrolyte resistance of each sample was determined by the

AC Impedance Analysis
The electrical behavior of the solid flexible polymer blend electrolytes was investigated via the AC impedance method. Figure 5 shows the Nyquist plots of pure PVA-PVP and PVA-PVP-NaSCN polymer blend electrolytes with different concentrations (5, 10, 15, 20, 25 wt% NaSCN) at room temperature. The graph shows a semicircle in the high-frequency region and a spike in the low-frequency region. The presence of the semi-circle is due to the volume effect of the electrolyte and the spike is caused by the blocking effect of the electrodes [30]. The bulk electrolyte resistance of each sample was determined by the intercept between the semi-circle and the spike. The addition of 5 wt% NaSCN to PVA: PVP (50:50 wt%) has considerably shrunk the diameter of the semi-circle which suggests a decrease in bulk resistance in NaSCN-based polymer blend electrolyte. This reduction may be related to the increase in the number of ionic charges upon the addition of NaSCN. The addition of more salt indicates the appearance of a spike only, which suggests that the PEs' resistive component exists [31].

Conductivity
The conductivity of each sample was calculated at room temperature using Equation (1) and it is summarized in Table 1. These values are calculated using data obtained in Figure 5. It should be noted that the conductivity polymer blend (PVA-PVP) is shown to be superior to that of the pristine polymers. The maximum conductivity was obtained with the composition of PVA: PVP (50:50 wt%) + 20 wt% NaSCN and found to be 8.1 × 10 −5 S/cm with the lowest bulk resistance. The NaSCN concentration-dependent conductivity is shown in Figure 6.

Conductivity
The conductivity of each sample was calculated at room temperature using Equation (1) and it is summarized in Table 1. These values are calculated using data obtained in Figure 5. It should be noted that the conductivity polymer blend (PVA-PVP) is shown to be superior to that of the pristine polymers. The maximum conductivity was obtained with the composition of PVA: PVP (50:50 wt%) + 20 wt% NaSCN and found to be 8.1 × 10 −5 S/cm with the lowest bulk resistance. The NaSCN concentration-dependent conductivity is shown in Figure 6. It is evident that as the amount of NaSCN salt in the polymer blend increases, the conductivity rises. A slight increase in conductivity is observed after doping 15 wt% NaSCN. The addition of salt up to 20 wt% NaSCN has significantly increased the conductivity and further decreases at a higher amount of salt. This strong increase in conductivity is associated with an increase in the number of charge carriers in the PVA-PVP (50:50 wt%) blend matrix and the amorphous nature of the PVA-PVP blend PE which could be due to the interaction between Na + ions and C=O stretching bonds present in pure PVA and PVP. The further decrease in conductivity can be assigned to the increased number of ion aggregates (clusters) in the polymer blend matrix reducing the mobility of charge carriers [32]. The use of NaSCN as an additive material in the PVA: PVP (50:50 wt%) matrix has promoted the transport of Na + and favors the formation of ion-pair complexes. This led to reduced bulk resistance and thus improves the conductivity.
To sum up, the results obtained with the EIS plots and conductivity plots are wellcorrelated. EIS data revealed that the addition of NaSCN up to 5 wt% NaSCN showed a significant change in the conductivity trend due to the impact of salt in the polymer blend matrix which influences the conductivity. The incorporation of the salt between 5 and 20 wt% showed a significant reduction of the bulk electrolyte resistance due to NaSCN which improves the conductivity. This result was also confirmed by the data obtained with the conductivity plot, which shows a crucial increase in conductivity between 0 and 20 wt% NaSCN. In addition, the maximum value of the conductivity obtained with the composition 20 wt%NaSCN is also confirmed with the EIS data which indicates the lowest value of the bulk resistance. Finally, the shrinking effect of the semicircle observed in the EIS plot was due to the salt addition and this is confirmed by the increase in conductivity observed in the conductivity plot.

Dielectric Constant
The variation of the dielectric constant (ℇ) with the content of NaSCN in PVA-PVP PE is shown in Figure 7. The initial rise in the dielectric constant is brought on by an increase in charge carriers, and the subsequent fall is brought on by the blocking effect of the layer due to the accumulation of ion clusters in the PE. It is seen that the relative permittivity and the conductivity increase with the addition of salt which is correlated to the It is evident that as the amount of NaSCN salt in the polymer blend increases, the conductivity rises. A slight increase in conductivity is observed after doping 15 wt% NaSCN. The addition of salt up to 20 wt% NaSCN has significantly increased the conductivity and further decreases at a higher amount of salt. This strong increase in conductivity is associated with an increase in the number of charge carriers in the PVA-PVP (50:50 wt%) blend matrix and the amorphous nature of the PVA-PVP blend PE which could be due to the interaction between Na + ions and C=O stretching bonds present in pure PVA and PVP. The further decrease in conductivity can be assigned to the increased number of ion aggregates (clusters) in the polymer blend matrix reducing the mobility of charge carriers [32]. The use of NaSCN as an additive material in the PVA: PVP (50:50 wt%) matrix has promoted the transport of Na + and favors the formation of ion-pair complexes. This led to reduced bulk resistance and thus improves the conductivity.
To sum up, the results obtained with the EIS plots and conductivity plots are wellcorrelated. EIS data revealed that the addition of NaSCN up to 5 wt% NaSCN showed a significant change in the conductivity trend due to the impact of salt in the polymer blend matrix which influences the conductivity. The incorporation of the salt between 5 and 20 wt% showed a significant reduction of the bulk electrolyte resistance due to NaSCN which improves the conductivity. This result was also confirmed by the data obtained with the conductivity plot, which shows a crucial increase in conductivity between 0 and 20 wt% NaSCN. In addition, the maximum value of the conductivity obtained with the composition 20 wt%NaSCN is also confirmed with the EIS data which indicates the lowest value of the bulk resistance. Finally, the shrinking effect of the semicircle observed in the EIS plot was due to the salt addition and this is confirmed by the increase in conductivity observed in the conductivity plot.

Dielectric Constant
The variation of the dielectric constant (ε) with the content of NaSCN in PVA-PVP PE is shown in Figure 7. The initial rise in the dielectric constant is brought on by an increase in charge carriers, and the subsequent fall is brought on by the blocking effect of the layer due to the accumulation of ion clusters in the PE. It is seen that the relative permittivity and the conductivity increase with the addition of salt which is correlated to the carrier's concentration. The value of the relative permittivity with the salt content in PVA-PVP-NaSCN PE was calculated using Equations (2) and (3) Figure 8 depicts the number of charge carriers and mobility in the PVA-PVP polymer blend system at room temperature as a function of salt concentration. It is observed that the carrier concentration and mobility are opposed to each other. The initial rise in the number of charge carriers upon the addition of 5 wt% NaSCN and further increase up to 20 wt% are due to the augmentation of ion-pair complexes in the polymer-salt complex which increases the conductivity. The dip at 15 wt% is related to the ion agglomerations which do not contribute to the conductivity. A decrease in carrier density at the high content of NaSCN is due to the excess amount of ion clusters in the polymer blend matrix. At a lower amount of salt, the small number of charge carriers in the matrix allows the polymer chain to move more easily, increasing its mobility. At high content, salt in the PVA-PVP (50:50 wt%) matrix acts as an ion source and behaves as a plasticizer at a lower amount improving the chain mobility. However, conductivity is monitored by the carrier concentration. The density of charge carriers and mobility are calculated for different amounts of NaSCN in PE systems at room temperature using Equations (4) and (5) and given in Table 3.   Figure 8 depicts the number of charge carriers and mobility in the PVA-PVP polymer blend system at room temperature as a function of salt concentration. It is observed that the carrier concentration and mobility are opposed to each other. The initial rise in the number of charge carriers upon the addition of 5 wt% NaSCN and further increase up to 20 wt% are due to the augmentation of ion-pair complexes in the polymer-salt complex which increases the conductivity. The dip at 15 wt% is related to the ion agglomerations which do not contribute to the conductivity. A decrease in carrier density at the high content of NaSCN is due to the excess amount of ion clusters in the polymer blend matrix. At a lower amount of salt, the small number of charge carriers in the matrix allows the polymer chain to move more easily, increasing its mobility. At high content, salt in the PVA-PVP (50:50 wt%) matrix acts as an ion source and behaves as a plasticizer at a lower amount improving the chain mobility. However, conductivity is monitored by the carrier concentration. The density of charge carriers and mobility are calculated for different amounts of NaSCN in PE systems at room temperature using Equations (4) and (5) and given in Table 3.

Linear Speed Voltammetry (LSV)
The decomposition voltage was determined using the prepared solid flexible PE embedded within two stainless steels (SS). Figure 9 shows the LSV plot of the optimized SPE: PVA-PVP (50:50 wt%) + 20 wt% NaCN performed at the scan of 100 mV/s over the range 0-2.5 V. It is clear that no significant current appears over the range 0-1.475 V. Beyond 1.5 V, there is a sharp increase in the current density which is assigned to the decomposition of PE [33]. This assumes that the optimized electrolyte film is stable up to 1.5 V. It is wellknown that the typical value of the electrochemical stability potential window (ESPW) for protonic devices is around 1.0 V [34]. Therefore, the optimized PVA-PVP-NaSCN film can be suited for protonic devices.

Linear Speed Voltammetry (LSV)
The decomposition voltage was determined using the prepared solid flexible PE embedded within two stainless steels (SS). Figure 9 shows the LSV plot of the optimized SPE: PVA-PVP (50:50 wt%) + 20 wt% NaCN performed at the scan of 100 mV/s over the range 0-2.5 V. It is clear that no significant current appears over the range 0-1.475 V. Beyond 1.5 V, there is a sharp increase in the current density which is assigned to the decomposition of PE [33]. This assumes that the optimized electrolyte film is stable up to 1.5 V. It is well-known that the typical value of the electrochemical stability potential window (ESPW) for protonic devices is around 1.0 V [34]. Therefore, the optimized PVA-PVP-NaSCN film can be suited for protonic devices.

Transference Number Measurements
The Wagner's polarization method was used to assess how ions and electrons contributed to the total conductivity of the optimized PE. An applied voltage of 0.8 V was given to polarize the cell containing the optimized PE film: PVA-PVP (50:50 wt%) + 20 wt% NaCN. The current was recorded as a function of the time as shown in Figure 10. The curve shows a gradual decrease till its reaches a steady-state current (I ss = 5.34 × 10 −9 A). The total current (I t = 2.92 × 10 −7 A) takes into consideration both ions and electrons at the interface between SS and SPE. The steady-state current confirms the polarization of the cell due to the blocking effect of SS electrodes; however, it allows only the electrons to migrate through [35][36][37]. The ion contribution (t ion ) and electron contribution (t elec ) were calculated using Equations (6) and (7) and found to be 0.99 and 0.01 respectively. This result clearly indicates that the conductivity is monitored by ions as the contribution of electrons is very low.

Transference Number Measurements
The Wagner's polarization method was used to assess how ions and electrons contributed to the total conductivity of the optimized PE. An applied voltage of 0.8 V was given to polarize the cell containing the optimized PE film: PVA-PVP (50:50 wt%) + 20 wt% NaCN. The current was recorded as a function of the time as shown in Figure 10. The curve shows a gradual decrease till its reaches a steady-state current ( = 5.34 × 10 ).
The total current ( = 2.92 × 10 ) takes into consideration both ions and electrons at the interface between SS and SPE. The steady-state current confirms the polarization of the cell due to the blocking effect of SS electrodes; however, it allows only the electrons to migrate through [35][36][37]. The ion contribution ( ) and electron contribution ( ) were calculated using Equations (6) and (7) and found to be 0.99 and 0.01 respectively. This result clearly indicates that the conductivity is monitored by ions as the contribution of electrons is very low.

Cyclic Voltammetry
The performance of the supercapacitor has been evaluated via the CV approach at a scan rate of 50 mV/s over the range of 0-0.8 V for three cycles. Figure 11 shows the capacitive behavior of the fabricated device, which reveals the hysteresis buckle of a supercapacitor. The existence of the supercapacitor was asserted by the presence of no redox peak which suggests the non-faradaic process implied during the charge storage [38]. The CV graph indicates that the total capacitance in the optimal sample is spread over 0-0.8 V and this denotes the importance of the surface area and narrow pore distribution. The supercapacitor gets charged at the electrical double layer due to the induced electric field which holds the ions from the electrolyte and polarizes electrons from the electrode. The CV graph has been recorded to check the device's performance. The specific capacitance of the supercapacitor device was calculated from the CV graph using Equation (8) and found to be 13.28 F/g.

Cyclic Voltammetry
The performance of the supercapacitor has been evaluated via the CV approach at a scan rate of 50 mV/s over the range of 0-0.8 V for three cycles. Figure 11 shows the capacitive behavior of the fabricated device, which reveals the hysteresis buckle of a supercapacitor. The existence of the supercapacitor was asserted by the presence of no redox peak which suggests the non-faradaic process implied during the charge storage [38]. The CV graph indicates that the total capacitance in the optimal sample is spread over 0-0.8 V and this denotes the importance of the surface area and narrow pore distribution. The supercapacitor gets charged at the electrical double layer due to the induced electric field which holds the ions from the electrolyte and polarizes electrons from the electrode. The CV graph has been recorded to check the device's performance. The specific capacitance of the supercapacitor device was calculated from the CV graph using Equation (8) and found to be 13.28 F/g.  Figure 12 shows a galvanostatic charge-discharge curve of a supercapacitor made with GO coated on graphene electrodes. Potential is measured with respect to time by applying a fixed current density of 0.5 A g −1 . It is observed a voltage drop, indicating the presence of internal resistance in the structure. The linear charge/discharge curve clearly reveals the capacitor behavior of the structure with less Faradic process and low ESR value. The coulombic efficiency of the GO-based system is calculated using Equation (9) and found to be 100%, the system delivers the charge for a long duration. The specific capacitance of the device was also calculated from the galvanostatic charge/discharge curve shown in Figure 12 using Equation (10). The calculated specific capacitance value was 12.15 F/g at 0.5 A g −1 . Figure 11. CV plot of the supercapacitor based on the optimized polymer-salt blend electrolyte film recorded at a scan rate 50 mV/s over the potential range 0-0.8 V for the three first cycles. Figure 12 shows a galvanostatic charge-discharge curve of a supercapacitor made with GO coated on graphene electrodes. Potential is measured with respect to time by applying a fixed current density of 0.5 A g −1 . It is observed a voltage drop, indicating the presence of internal resistance in the structure. The linear charge/discharge curve clearly reveals the capacitor behavior of the structure with less Faradic process and low ESR value. The coulombic efficiency of the GO-based system is calculated using Equation (9) and found to be 100%, the system delivers the charge for a long duration. The specific capacitance of the device was also calculated from the galvanostatic charge/discharge curve shown in Figure 12 using Equation (10). The calculated specific capacitance value was 12.15 F/g at 0.5 A g −1 .

Low Frequency-Impedance Spectroscopy (IS)
The supercapacitor device's performance was also evaluated via IS approach at the low-frequency region, described by a capacitive spike indicating the formation of the ca-

Low Frequency-Impedance Spectroscopy (IS)
The supercapacitor device's performance was also evaluated via IS approach at the low-frequency region, described by a capacitive spike indicating the formation of the capacitance double layer and charge accumulation at the contact between the electrode and electrolyte. Figure 13 shows the low-frequency experimental impedance spectroscopy graph of the supercapacitor cell using the maximum solid flexible ion-conducting PE: PVA-PVP (50:50 wt%) + 20 wt% NaCN over the frequency range 1 MHz to 0.05 mHz. The fitting plot was obtained by simulation of the modified Randal's equivalent circuit [39,40], involving the resistance at high frequency (R HFR ), the diameter of the first semi-circle (R 1 ), which is assigned to the contact resistance between cathode and electrolyte, the diameter of the second semi-circle (R 2 ) refers to the charge transfer resistance, Q 1 and Q 2 are the constant phase elements associated to R 1 and R 2 respectively. R HFR and R 1 take into consideration the bulk and transport properties. R 2 , Q 1 , Q 2 feature the insulating and dielectric properties at the electrode and the electrolyte. It is clearly observed that the fitting plot overlaps slightly with the experimental impedance curve. The specific capacitance was calculated at low frequencies (f = 0.03 mHz) using Equation (11), and was found to be 14.25 F/g which is almost close to 13.28 F/g obtained with the CV graph. Table 4 summarizes the value of the different parameters obtained via the EIS data fitted with the equivalent electrical circuit (EEC).  This calculated capacitance value was found to be higher than 1.41 F/g obtained at a rate scan of 10 mV/s with the system PVA: Mg (CF3SO3)2 prepared by Francis et al. [41]. This demonstrates the role of the amorphous structure of PVP in polymer blend electrolyte (PVA-PVP-NaSCN) which could have reinforced the contact between the electrolyte and the active material, limiting the interface resistance and the capacity loss. The low  This calculated capacitance value was found to be higher than 1.41 F/g obtained at a rate scan of 10 mV/s with the system PVA: Mg (CF 3 SO 3 ) 2 prepared by Francis et al. [41]. This demonstrates the role of the amorphous structure of PVP in polymer blend electrolyte (PVA-PVP-NaSCN) which could have reinforced the contact between the electrolyte and the active material, limiting the interface resistance and the capacity loss. The low specific capacitance obtained is related to the PE properties although exhibiting good conductivity. However, the specific capacitance strongly depends on the surface area of the electrode material used and also the interface resistance between the active material and the PE. Tough, the specific capacitance can be enhanced by intercalating solidified chemicals into stacked GO sheets to improve the surface area of the electrode as reported by Yi Zhao and his co-workers [42], this study was rather focused on improving the performance of the PE instead of electrode material (GO).
To sum up, the incorporation of PVP and NaSCN into the PVA matrix has not only improved the specific capacitance of the supercapacitor but also significantly increased the number of charge carriers and mobility for the PVA: PVP: NaSCN polymer blend electrolyte. The conductivity of the optimal system: PVA: PVP (50:50 wt%) + 20 wt% NaSCN was found to be one order of magnitude higher than that of the PVA: CS: LiClO 4 polymer blend system reported by Rathod et al. [43] who obtained a maximum value of 3 × 10 −6 S/cm for 20 wt%LiCO4 at room temperature without PVP and NaSCN. In another study, the PVA: CS: NH 4 I system exhibited a maximum conductivity of 7.69 × 10 −7 S/cm for the optimal salt concentration of 40 wt% of NH 4 I [44], which is found to be lower by two orders of magnitude as compared to the PVA: PVP: NaSCN system. This suggests that insertion of NaSCN into the PVA: PVP matrix is favorable for the formation of more ion-dipole interactions and the increase of the amorphous phase due to complexation between Na + cations and the reactive functional groups of PVA: PVP blend present in the PE which augmented the number of mobile species and thus enhances the conductivity. Table 5 shows the ionic conductivity and t ion values obtained for the recently prepared solid polymer electrolytes and the presently used polymer electrolytes. Table 5. Summary of the ionic conductivities and t ion values for some recent solid electrolyte systems and the optimized solid flexible polymer electrolyte (PVA: PVP + 20 wt% NaSCN) prepared in this work.

Samples
Ionic Conductivity (S cm −1 ) t ion TNM References

Conclusions
New solid flexible polymer blend electrolytes based on PVA, PVP, and NaSCN salt as an additive material to improve the conductivity, have been successfully developed via the casting method, and the optimized solid flexible electrolyte was used in a supercapacitor device. FTIR data confirmed the formation of a complex between PVA, PVP, and NaSCN upon the addition of salt (NaSCN) which changed the chemical structure of the whole electrolyte. This result was also verified with POM data which showed a modification of the surface morphology of the matrix due to the salt effect and the formation of the amorphous phase. Impedance spectra demonstrated a significant diminution in bulk resistance due to the salt dispersion which increased the conductivity. The optimized solid flexible polymer blend electrolyte was found to be 8.1 × 10 −5 S/cm with a concentration of charge carriers of 1.94 × 10 17 and mobility of 2.61 × 10 −1 m 2 /Vs. The highly conductive PE is electrochemically stable up to 1.5 V which was prominent for protonic devices since the conventional potential value is 1 V. The conductivity was controlled by ions as the ion transference number was approximately 0.99 for the high ion-conducting polymer blend system: PVA: PVP (50:50 wt%) + 20 wt% NaSCN. The supercapacitor device was fabricated with the optimized PE film and tested. GCD curve reveals an ideal linear charge/discharge behavior with a coulombic efficiency of 100%, and the system delivers the charge for a long duration. The supercapacitor demonstrated a specific capacitance of 13.28 F/g via the CV approach which was close to 14.25 F·g −1 obtained with impedance data at low frequency.

Data Availability Statement:
The data presented in this study are available on request from the corresponding author.