Characteristics of a Plasticized PVA-Based Polymer Electrolyte Membrane and H+ Conductor for an Electrical Double-Layer Capacitor: Structural, Morphological, and Ion Transport Properties.

Poly (vinyl alcohol) (PVA)-based solid polymer electrolytes doped with ammonium thiocyanate (NH4SCN) and glycerol were fabricated using a solution casting method. Lithium-based energy storage devices are not environmentally friendly materials, and they are toxic. Thus, proton-conducting materials were used in this work as they are harmless and are smaller than lithium. The interaction between PVA and the electrolyte elements was shown by FTIR analysis. The highest conductivity of 1.82 × 10-5 S cm-1 was obtained by the highest-conducting plasticized system (PSP_2) at room temperature. The mobility, diffusion coefficient, and number density of anions and cations were found to increase with increasing glycerol. FESEM was used to investigate the influence of glycerol on film morphology. TNM showed that the cations and anions were the main charge carriers. LSV showed that the electrochemical stability window of the PSP_2 system was 1.99 V. The PSP_2 system was applied in the preparation of an electrical double layer capacitor device. The shape of the cyclic voltammetry (CV) curve was nearly rectangular with no Faradaic peaks. From the galvanostatic charge-discharge analysis, the power density, energy density, and specific capacitance values were nearly constant beyond the first cycle at 318.73 W/Kg, 2.06 Wh/Kg, and 18.30 F g-1, respectively, for 450 cycles.

1. Introduction

There are two main kinds of electrochemical supercapacitors as categorized by the mechanism of energy storage: (1) electrical double-layer capacitor (EDLC) and (2) electrochemical pseudocapacitor (PSc) [1,2]. An EDLC can store charges in the double-layer at the interfaces between the electrolytes and electrode, while the PSc sustains a charge transfer reaction (Faradaic reaction) between the electrolytes and electrode in an appropriate potential window. Activated carbon (AC) electrode materials with a large surface area of 2500 m2/g have been used for EDLCs [3]. The large surface area of AC causes more electrosorption of NH4+ cations and SCN− anions, and this leads to a higher capacitance. Furthermore, AC porosity is imperative in the preparation of EDLCs with higher capacitance.

The use of solid polymer electrolytes (SPEs) as separators in electrochemical energy storage devices, such as supercapacitors and batteries, causes a decrease in reactivity and in leakage issues related to the liquid electrolyte. In addition, SPEs can provide desired shapes, better safety, and good flexibility. However, their low conductivity, poor interfacial stability between electrodes, and poor mechanical strength are still issues for researchers [4,5]. To provide better conductivity of SPEs, numerous methods have been used, such as the addition of ionic liquids and plasticizers and the blending of polymers to form blended and plasticized polymer electrolytes (PEs) [6,7], gel polymer electrolytes [8], and ionic liquid-based PEs.

In this work, a poly (vinyl alcohol) (PVA)-based SPE incorporated with ammonium thiocyanate (NH4SCN) and glycerol was successfully prepared, and the plasticized electrolyte was used for the preparation of an EDLC device. Ammonium salts are broadly used in proton-conducting PEs because they are good proton donors [9]. NH4SCN salt has a lattice energy of 605 kJ/mol and thus is easily dissociated into cations and anions when it is dissolved in the water solvent, therefore, NH4SCN delivers more ammonium ions to the polymer [9]. Hemalatha et al. [9] prepared PVA/amino acid proline doped with different concentrations of NH4SCN. The authors showed that the amorphous phase and conductivity increased by adding 0.4 and 0.5 Mwt% NH4SCN, while they decreased with 0.6 Mwt% NH4SCN. Hema et al. obtained the conductivity of 10−5 S cm−1 for the system of PVA/NH4Cl [10]. Asnawi et al. [11] prepared a PE system of chitosan/dextran-NaTf with different glycerol concentrations. The plasticized electrolyte with the highest conductance had a maximum direct current (DC) ionic conductivity of 6.10 × 10−5 S/cm. The author used the electrolyte for application in electrochemical energy storage devices. Dey et al. [12] fabricated polyethylene oxide (PEO)/potassium iodide (KI) PEs. The authors showed the effect of the filler of nanosized ceria (CeO2~10 nm) on ionic conductivity in the PE of PEO/KI. They showed that the addition of the nanoparticles (NPs) increased the conductivity by two orders of magnitude. The authors indicated that the ionic conductivity increased with the addition of KI salt. The conductivity was more increased by the incorporation of CeO2 NPs. The maximum conductivity of 2.15 × 10−3 S cm−1 was achieved for 20 wt. % of CeO2 doped-PE composite. PVA is biocompatible and biodegradable, and it is non-toxic. Shuhaimi et al. [13] documented that H+ ions are the conducting charges, which mobilize in the κ-carrageenan/chitosan/NH4NO3 system. It has been described that H+ ions in the PEO/NH4SCN system are the conducting charges [14]. In this research, glycerol was used to improve conductivity. Plasticizers can improve the amorphous structure of the PEs [3]. Pawlicka et al. [15] increased the conductivity from around 10−8 to 10−4 S cm−1 by the addition of glycerol in their electrolytes. Based on an elastic poly (acrylic acid) (PAA)-based gel electrolyte film, eutectic gallium-indium liquid metal (EGILM) anode, and carbon fiber yarn coated by a Pt nanoflower array as the cathode, Liu et al. [16] showed a cable-shaped, highly elastic, soft, discharge-current-controllable liquid metal–air battery with high flexibility, high discharge performance, and low operating temperature. The energy concerns and related environmental problems have made the study of energy fields and electrochemical energy storage devices a hot subject since the beginning of 21st century. Each year, thousands of scientific works on electrochemical energy storage devices are published. Through our research in this area, we intend to create commercially viable polymer electrolyte-based electrochemical energy storage devices. Attaining this aim requires testing of different polymer-based electrolyte systems, and improving various properties of the polymer electrolyte so as to reach the best solution. Using biodegradable polymer-based electrolytes, for example PVA, can have both economic and environmental benefits. Lithium-based electrochemical energy storage devices are not eco-friendly materials and they are poisonous. Instead, proton-conducting species are smaller than lithium and they are harmless. In this work, a proton-conducting PVA-based electrolyte is fabricated for the use in an EDLC device.

2. Materials and Methods

2.1. Materials

Glycerol with a molecular weight (Mw) of 92.09382 g/mol and PVA with an average Mw of 85,000–124,000 was purchased from Sigma-Aldrich. NH4SCN with a Mw of 76.12 g·mol−1, n-Methyl-2-pyrrolidone with a Mw of 99.13 g·mol−1, and carbon black with a Mw of 12.01 g·mol−1 were purchased from HmbG chemicals, EMPLURA, and Timcal, respectively (Kuala Lumpur, Malaysia). Activated carbon with a Mw of 12.01 g·mol−1 and polyvinylidene fluoride with an average Mw of ~534,000 by GPC were purchased from Magna value.

2.2. Electrolyte Preparation

First, 50. wt. % PVA was dissolved in 40 mL distilled water, and it was stirred with a magnetic stirrer at 85 °C for 65 min for the preparation of a PVA solution and was allowed to cool to room temperature (RT). The solutions of PVA were combined with 50 wt. % NH4SCN and stirred with a magnetic stirrer at RT until the NH4SCN in the solutions was dissolved. Lastly, PVA/NH4SCN was plasticized with 30 and 40 wt. % glycerol, and it was coded as PSP_1 and PSP_2, respectively. The elements of the solutions were stirred to prepare a homogeneous solution and then kept at RT in the plastic Petri dishes for drying. For more drying, the samples were kept in a desiccator with blue silica gel before characterization and preparation of the EDLC device.

2.3. Characterization Techniques

2.3.1. Fourier Transform Infrared Spectroscopy (FTIR)

To investigate the PSP_1, PSP_2, and PVA films, an FTIR Spectrophotometer (Malvern Panalytical Ltd., Malvern, UK) was used in the wavenumber range 4000 to 450 cm−1 using a resolution of 2 cm−1.

2.3.2. Field Emission Scanning Electron Microscopy (FESEM)

An Hitachi SU8220 (FEI Quanta 200 FESEM, FEI Company, Hillsboro, OR, USA) was used to conduct FESEM at a magnification of 500× to study the film’s morphology.

2.3.3. Electrochemical Impedance Spectroscopy (EIS)

The impedance data of PSP_1, PSP_2, and PVA films were taken using an EIS (3532-50 LCR HiTESTER (HIOKI), Nagano, Japan) between 50 Hz and 5 MHz. The films were cut into circles with a radius of 1 cm, and the films were inserted between two stainless steel (SS) electrodes by spring pressure. The imaginary and real parts (Z″ and Z′) of the complex impedance (Z*) data were measured by connecting the cell with a computer program.

2.4. Electrolyte Characterization

Transference Number Measurement (TNM) and Linear Sweep Voltammetry (LSV)

The TNM of ions (t) and TNM of electrons (t) were measured. The arrangement of the cell was SS|PSP_2|SS, and it was connected to a V&A Instrument DP3003 digital DC power supply and UNI-T UT803 multimeter. The applied voltage was 0.2 V at RT and the cell was polarized with time.

The electrochemical stability window (ESW) of the PSP_2 was measured using an LSV employing a DY2300 potentiostat at a scan rate of 10 mV s−1 and with a potential between 0 and 2.5 V.

2.5. Electrode Preparation

The preparation of the activated carbon electrodes was shown in our previous work in detail [3].

2.6. EDLC Characterization

The activated carbon (AC) electrode was cut into circles with an area of 2.01 cm2. The PSP_2 was inserted between the electrodes and then placed in a CR2032 coin cell. After that, the CR2032 was placed in a Teflon case as indicated in Figure 1.

Figure 1

Schematic diagram of the electrical double-layer capacitor (EDLC) setup.

3. Results and Discussion

3.1. FTIR Analysis

The FTIR for PVA/NH4SCN/glycerol and PVA are shown in Figure 2a,b. The modifications in the spectral features were seen when the PSP_1 and PSP_2 were compared with the PVA. The O–H stretching is the cause for the broad peak at 3303 cm−1 [17,18], while there were a shift and decrease in its intensity in the plasticized PVA due to the interaction between the elements of the electrolyte. Asymmetric stretching of C–H is associated with a peak at 2902 cm−1 [17], and its intensity is shifted and decreased in the case of plasticized PVA.

Figure 2

FTIR spectra for (i) pure poly (vinyl alcohol) (PVA), (ii) PSP_1, and (iii) PSP_2 from (a) 450 to 1900 cm−1 and (b) 1900 to 4000 cm−1.

The new intense and strong peak that emerged at 2043 cm−1 is related to aromatic S–C = n stretching of SCN− of the salt, while its intensity is shifted and falls with increasing glycerol by the interaction of the PVA with the electrolyte elements (see Figure 2b) [9,19]. As one of four H+ in the tetrahedral NH4+ connected to the nitrogen atom is weakly bound, H+ transfers to the coordination sites in PVA. The shift in the peak and the new peak in the plasticized PVA shows the interaction between the NH4SCN and the PVA [9]. The plasticizer can dissociate more salts to cations and anions and thus more ions are created to interact with the PVA [20].

C=O stretching of the acetate group is related to the absorption band at 1638 cm−1 in PVA [21], while it shifted to smaller wavenumbers in the plasticized PVA. The C–H bending of CH2 wagging is related to the band at 1412 cm−1 in PVA, and C–H deformation is related to the band at 1318 cm−1 in PVA (see Figure 2a,) [21]. The intensity of the two peaks was decreased and shifted in the plasticized PVA due to the interaction between the electrolyte elements.

In addition, the –C–O– stretching in PVA is the source for the band at 1080 cm−1 [22], which is decreased and shifted in its intensity in PSP_1 and PSP_2, as indicated in Figure 2a. C–H rocking in PVA is the cause for the band at 833 cm−1 (see Figure 2a,) [18]. In the plasticized PVA films, the intensity of the peak decreased and shifted, while a 40 wt. % glycerol addition caused a noticeable decrease in the intensity of the peak. These results are shown in Table 1.

Table 1

The FTIR results of PVA and plasticized systems.

Assignments	Wavenumber (cm−1)
	PVA	PSP_1	PSP_2
O–H stretching	3303	3305	3309
C–H stretching	2902	2914	2909
Aromatic S–C = n stretching	-	2043	2042
C=O stretching	1638	1609	1605
C–H bending of CH2	1412	1407	1413
C–H deformation	1318	1310	1309
–C–O– stretching	1080	1029	1038
C–H rocking	833	831	822

3.2. Impedance Analysis

Figure 3a–c shows the Nyquist plot for each film of plasticized PVA and PVA at ambient temperature. The bulk resistance (R) is measured using the intersection of the line with a real axis. The R reduces as the glycerol is increased to 40 wt. % owing to the increase of the mobility of carriers, and thus the conductivity increases [23].

Figure 3

EIS for (a) PVA, (b) PSP_1, and (c) PSP_2at room temperature (RT).

The model of an electrical equivalent circuit (EEC) is used to fit the EIS data because it is a simple method [24]. The R is measured by the intersection between the semicircle and the horizontal axis at the low frequency region. The pure PVA consists of only a semicircle, while with the addition of 30 and 40 wt. % glycerol (PSP_1 and PSP_2), the EIS consists of a tail and one semicircle at the regions of low and high frequencies, respectively as shown in Figure 3a–c. The semicircle is associated with the anions and cations conduction at the bulk of the system [25]. It has been reported that the bulk conductivity is related to the parallel connection of bulk capacitance and R of the electrolyte [26]. The spike line is due to the migration of ions at the electrolyte and electrode interfaces [27].

The Nyquist plots for the pure PVA are interpreted as a combination of a constant phase element (CPE1) and R for the carriers in the electrolytes, while the PSP_1 and PSP_2 systems are interpreted as a combination of R and two CPEs (CPE1 and CPE2), as indicated in the insets of Figure 3a–c [28].

The impedance of Z is shown as [29,30]: where ω, C, and p are the angular frequency, capacitance of CPE, and deviation of the Cole–Cole plots from the vertical axis, respectively.

The imaginary and real parts (Z and Z) of the impedance related to the EEC (inset of Figure 3a) are interpreted as:

The Z and Z associated with the EEC as presented in the inset of Figure 3b,c are interpreted as: where C1 is the bulk capacitance of CPE1 and C2 is the capacitance of CPE2 at the interface between the electrode and the electrolyte. The EEC fitting parameters are indicated in Table 2.

Table 2

The EEC fitting parameters for PVA, PSP_1, and PSP_2 at RT.

Sample	P1 (rad)	P2 (rad)	K1 (F−1)	K2 (F−1)	C1 (F)	C2 (F)
PVA	0.79	-	3.6 × 1010	-	2.78 × 10−11	-
PSP_1	0.86	0.40	2.2 × 109	1.6 × 105	4.55 × 10−10	6.25 × 10−6
PSP_2	0.87	0.69	3.8 × 108	1.09 × 105	2.63 × 10−9	9.17 × 10−6

By taking R and the electrolyte dimensions, the DC conductivity (σ) is measured using the Equation (6) [31,32], where A and t are the area of the SS electrodes and thickness of the electrolyte, respectively. The electrolytes’ conductivities are shown in Table 3. Based on the previous study, the conductivity of 10−5 S cm−1 is reasonable for use in energy storage devices [11,33].

Table 3

The conductivity of the films at RT.

Symbol	PVA (wt. %)/NH4SCN (wt. %)/Glycerol (wt. %)	σdc (S cm−1)
Pure PVA	50:00:00	2.87 × 10−11
PSP_1	50:50:30	5.45 × 10−7
PSP_2	50:50:40	1.82 × 10−5

It was previously shown that the incorporation of NH4NO3 (30 wt. %) into a potato starch/methyl cellulose blend system improved the conductivity to (4.37 ± 0.16) × 10−5 S cm−1 [34]. In this study with 40 wt. % of glycerol, the DC conductivity increased to 1.82 × 10−5 S cm−1. Plasticization causes an increase in the dissociation and forms salt-conducting pathways for the transportation of mobile cations and anions, which increase the conductivity [35]. The large dielectric constant of glycerol can decrease the electrostatic force between anions and cations of the salt and thus deliver more mobile ions. The existence of plasticizer can increase the amorphous nature of the PE and thus increase the ionic conductivity [29]. Hamsan et al. [29] documented that the decrease of conductivity by the addition of 50 wt. % glycerol is attributed to the arrangement of self-linkages of plasticizer, causing recrystallization of the salt, which causes a decrease in conductivity.

As the impedance data of the PSP_1 and PSP_2 systems consist of a spike and one semicircle, the number density (n), diffusion coefficient (D), and mobility (μ) of ions are obtained using the relations below [36,37,38]:

The D of the plasticized systems is measured using Equation (7). where ε and ε are the dielectric constant and the permittivity of the vacuum, respectively. τ is the reciprocal of ω corresponding to the smallest value in Z.

The mobility (µ) of the plasticized systems is measured using the equation of Nernst–Einstein, where T and k refer to the absolute temperature and Boltzmann constant, respectively.

Conductivity is indicated by

Hence, the number density of ions (n) is measured by Equation (10):

Table 4 lists the transport parameters of ions for the systems.

Table 4

The transport parameters of ions at RT.

Sample	D (cm2 s−1)	µ (cm2 V−1s)	n (cm−3)	D+ (cm2 s−1)	D− (cm2 s−1)	µ+ (cm2 V−1s)	µ− (cm2 V−1s)
PSP_1	7.27 × 10−9	2.83 × 10−7	1.20 × 1019	6.55 × 10−9	7.12 × 10−10	2.55 × 10−7	2.77 × 10−8
PSP_2	2.59 × 10−8	1.01 × 10−6	1.12 × 1020	2.34 × 10−8	2.54 × 10−9	9.11 × 10−7	9.9 × 10−8

As seen in Table 4, the D increased as the glycerol increased from 30 to 40 wt. %. A similar trend was noted for μ, as see in Table 4. The D and μ increments are related to the development of chain flexibility due to glycerol. The values of n, μ, and D increased with glycerol, which causes to increase in the conductivity, as more glycerol incorporation can dissociate further salts to free ions, and hence raise the n of ions [3].

3.3. Field Emission Scanning Electron Microscopy (FESEM)

Field emission scanning electron micrographs were taken at a 500× magnification for plasticized systems to support the EIS, and the micrographs for the systems are shown in Figure 4a,b. The white structures show the protruding salts within the sample’s surface in Figure 4a,b. When there is an addition of 30 wt. % glycerol into the system, a few salts emerged on the sample surface, as shown in Figure 4a. It is seen from the field emission scanning electron micrograph in Figure 4b that protruding salt structures were not obviously seen as the glycerol increased to 40 wt. % (PSP_2 system) compared with that seen for the PSP_1 electrolyte system. The glycerol plasticizer dissociates more salts into anions and cations and thus improves the value of the conductivity [29]. The PSP_2 film has a uniform and smooth surface morphology and has no phase separation. The field emission scanning electron micrographs are in good agreement with the EIS. The white structures decreased in the PSP_2 system and the R decreased as shown in the EIS plot, while conductivity increased. It has been reported that the smooth surface morphology is related to the amorphous structure development of the systems [39]. The smooth surface electrolyte can help conduct ions and allow them to migrate easily, and thus increase the DC ionic conductivity [39].

Figure 4

FESEM for (a) PSP_1 and (b) PSP_2 electrolyte systems at RT.

3.4. Dielectric Studies

The trend of conductivity is explained further using a dielectric study. The dialectic constant (ε) and dielectric loss (ε) are obtained using Equations (11) and (12) [40,41,42]: where ω and C are the radial frequency and the capacitance in a vacuum, respectively.

The influence of glycerol on dielectric parameters (ε and ε) is revealed in Figure 5a,b. The dielectric parameters at the low frequency region increase as the glycerol increases to 40 wt. %. More plasticizer increases the dissociation of ions, and thus provides more mobile ions and increases the conductivity [20].

Figure 5

Dielectric plot of (a) ε v log(f) and (b) ε v log(f) for pure PVA, PSP_1, and PSP_2 electrolyte systems at RT.

The agreement between conductivity () and the dielectric constant () was shown in previous studies [43,44,45,46,47,48,49,50,51,52,53]. In plasticized systems, ε and ε are low at the high frequency region owing to the swift periodic reversal of the electric field, while both parameters are high at the low frequency region as the blocking electrodes accumulate charges at the electrode/electrolyte interfaces [54,55].

3.5. Electrical Modulus Studies

The imaginary and real (M and M) parts of the complex electrical modulus (M) are measured using Equations (13) and (14) [56,57,58,59,60,61].

Figure 6a and Figure 7a show M against frequency for the pure PVA, PSP_1, and PSP_2 at RT. As seen in the diagram, dispersion is not seen at the low frequency region owing to polarization, and thus the M values are close to zero, while dispersion exists at the high frequency region [62]. The long tail at the region of low frequency is associated with the big value of capacitance at the interfaces of the electrodes and electrolytes [63]. Figure 6b and Figure 7b show M against frequency for the pure PVA and plasticized systems. In general, the M diagram is divided into two regions, which are low and high frequency regions. The low frequency is due to the mechanism of conduction, whereas the high frequency shows the relaxation process [64,65]. It can be seen that in the PSP_1 and PSP_2, the conductivity relaxation peaks appear.

Figure 6

Electric modulus of (a) M v log(f) and (b) M v log(f) for pure PVA film at RT.

Figure 7

Electric modulus of (a) M v log(f) and (b) M v log(f) for PSP_1 and PSP_2 electrolyte samples at RT.

3.6. EDLC Characteristics

3.6.1. Transference Number Measurement (TNM)

TNM for the ion (t) and TNM for the electron (t) for the PSP_2 sample were measured using the DC polarization method [3]. In this technique, DC voltage is used and the currents are measured against time, as shown in Figure 8. The PSP_2 film was placed between two SS electrodes and the t and t were measured using Equations (15) and (16) [3,29,66,67,68,69,70]: where steady state and initial current are referred to by I and I, respectively.

Figure 8

Polarization current vs. time for the highest plasticized sample (PSP_2) at RT.

The cell is polarized when the cell reaches the stationary state, and the transport of the remaining current is only owing to electrons as the SS electrodes block the cations and anions and allow the electrons to pass through it [71]. In the present study, t was 0.902, which is near to an ideal value, meaning that the transport mechanism is dominated by ions in the plasticized films. Shukur and Kadir [72] determined t values are in the range of 0.91 and 0.98 for the NH4Cl glycerol-based polymer electrolytes.

From the t and conductivity values, the mobility and diffusion coefficient of anions and cations of each plasticized system were measured using Equations (17)–(22) [73]. where k, T, σ, D, D+, μ+, and μ− are Boltzmann constant, absolute temperature, conductivity, electron charge, anion diffusion coefficient, cation diffusion coefficient, cation mobility, and anion mobility, respectively. The cations are smaller than the anions, and thus the μ is higher than the μ−. Table 4 reveals that the μ+ and D+ are higher than the μ− and D−. Once the conductivity is enhanced, the μ− and μ+ are increased. The same pattern was observed for D− and D+. So, the TNM shows that the conductivity is impacted by diffusion coefficient and mobility. The PSP_2 has the highest mobility and diffusion coefficient compared with those of the PSP_1 electrolytes.

3.6.2. Electrochemical Stability Study

In order to measure the electrochemical stability window (ESW) of PSP_2, linear sweep voltammetry (LSV) was used. The ESW of the electrolyte is composed of the working voltage limits in which the electrolyte can work safely without decomposing in a device. As shown in Figure 9, the ESW for the SPE film was 1.99 V, which is adequate for the application of the SPE in electrochemical energy storage devices [74,75,76], for example, in a supercapacitor. Hamsan et al. [29] found the ESW of 1.88 V for the system of potato starch/methyl cellulose/NH4NO3/glycerol and used the electrolyte for an EDLC application.

Figure 9

LSV for the highest plasticized sample (PSP_2) at RT.

3.6.3. Cyclic Voltammetry Study

The capacitive behavior was examined with the cyclic voltammetry (CV) technique for the cell. Figure 10 indicates the CV response for the EDLC at different scan rates, and the CV curves show a rectangular shape at a lower scan rate. Lack of electron contribution is confirmed by the lack of redox peaks, meaning that the EDLC shows a non-Faradic process [77].

Figure 10

Cyclic voltammetry (CV) curve for the highest plasticized sample (PSP_2) at RT.

The CV shapes move from a leaf shape to a rectangular one at lower scan rates. The move to a leaf-like shape of the CV curve from a rectangular one is due to carbon porosity and internal resistance, which form current and voltage dependence [78].

The specific capacitance from the CV curve (C) is determined using Equation (23) [33]: where ∫I(V)dV, a, m, V and V are the area of CV curve, scan rate, activate material mass, final (0.9 V), and initial voltages (0 V), respectively.

The values of C are seen in Table 5 in which the C increases at lower scan rates. Ions can fill the vacant sites inside the electrodes as the ions have enough time for the mechanism of diffusion at low scan rates, and thus the C is higher [79]. The C in this work (Table 5) is higher than those of previous works, for example, Hamsan et al. [29] used potato starch/methyl cellulose/NH4NO3/glycerol for an EDLC and measured a C of 20 F g−1 by the CV curve at 2 mV s−1. The CV profile in our study is similar to that indicated by Hamsan et al. [29].

Table 5

Capacitance from CV curves.

Scan Rate (mVs−1)	CCV (F g−1)
100	19.43
50	29.26
20	40.00
10	44.58
5	45.72

3.7. Galvanostatic Charge-Discharge (GCD) Analysis

Figure 11 reveals the GCD profiles at 0.5 mA cm−2 with potential from 0 to 1 V. The discharge profiles with nearly linear slope show the capacitive behavior of the EDLC [79], and thus the process of charge storage is based on the development of charges at the electrode/electrolyte interfaces.

Figure 11

GCD curve at 0.5 mA/cm2 for the EDLC at RT.

The initial voltage drop in the charge-discharge curves is primarily attributed to the internal resistance of the cell. The equivalent series resistance (ESR) is measured from the voltage drop, and it is presented in Figure 12. For the 450 cycles, ESR ranged from 245 to 278 Ω. A good contact among electrodes and SPEs is ensured by a small ESR, signifying that the journey of cations and anions toward the pore at the electrode’s surface will be easier [80]. Table 6 shows the comparison of the ESR of the EDLC with previous reports.

Figure 12

Equivalent series resistance (ESR) of the EDLC device for 450 cycles at RT.

Table 6

EDLC parameters using different polymer electrolytes at RT.

Electrolyte Systems	Specific Capacitance (F/g)	Energy Density (Wh/kg)	Power Density (W/kg)	ESR (Ω)	Cycle Number	Ref.
Chitosan/methyl cellulose (MC)/NH4I/glycerol	9.70	1.1	578.55	136–155	100	[86]
Chitosan-κ-carrageenan/NH4NO3	18.5	-	-	-	20	[13]
MC/NH4NO3/poly(ethylene glycol)	25	2.5	130	109	-	[28]
PVA/chitosan/NH4I/glycerol	19.4	5.48	380	75–330	250	[87]
MC/potato starch (PS)/NH4NO3/glycerol	31	3.1	910–385	29–64	1000	[29]
Chitosan/PS/NH4F	4.1	0.57	155	550	100	[88]
PVA/NH4SCN/glycerol	18.3	2.06	318.73	245–278	450	This work

The ESR of the EDLC is measure using Equation (24) [3]: where i and V are the working current and drop voltage before the discharging process, respectively.

The specific capacitance (C) from the galvanostatic charge-discharge (GCD) is measured using Equation (25) [3]: where x and i are the discharge gradient and working current, respectively. The C from the CV curve and C from GCD are compared. The C up to 450 cycles is shown in Figure 13. For the first cycle, the C value, measured by Equation (25), is obtained as 7.45 F g−1. The C value is increased and keeps nearly constant with the average value of ∼18.3 F g−1 for 450 cycles beyond the first cycle. This is because most of the cations and anions at the bulk of the electrolyte move gradually in opposite directions toward the surface of the electrodes to create a proper double layer. However, the C patterns have slightly dipped after the first cycle, which might be related to the contact between the electrode and electrolyte interfaces and an increase of the internal resistance at higher cycles. The long life cycle with stable capacitance is essential for an EDLC. Table 6 shows the comparison of the C of the EDLC with previous reports.

Figure 13

Specific capacitance of the EDLC device for the 450 cycles at RT.

Wei et al. [81] reported that polyethylene oxide (PEO)-based SPEs have large applications in all-solid-state Li-ion batteries. The authors used a simple and effective press-rolling method to decrease the crystallinity of the electrolyte. With the rolled PEO-based SPE, the LiFePO4/SPE/Li all-solid Li-ion battery provided a large rechargeable specific capacity of 162.6 mAhg−1 with a charge-discharge voltage gap of 60 mV at a current density of 0.2 C with a smaller capacity decay rate. They mentioned that the enhancement of the electrochemical properties was attributed to the method of press-rolling, resulting in a decreased activation energy and also a doubling of conductivity in comparison with those of the electrolyte fabricated by a traditional cast technique. Yu et al. [82] reported that in a fiber-shaped zinc-polyaniline battery (FZPB), the cathode with plasma-treated carbon fibers and a polyaniline loading of 0.158 mg mgCF−1 (i.e., 2.36 mg cmCF−1) showed a capacity retention of 95.39% after 200 cycles at 100 mA g−1 and a discharge capacity of 83.96 mA h g−1 at a large current density of 2000 mA g−1, which are ∼1.67 and 1.24 times those of the pure carbon-fiber-based battery, respectively. They also mentioned that the FZPB showed large flexibility with a capacity retention of 86.4% after bending to a radius of 2.5 mm for 100 cycles as a wearable energy device [82].

The other parameters (power density (P) and energy density (E)) are measured using Equations (26) and (27) [3,29]: where V is the applied voltage.

From Figure 14, the E is 0.84 Wh/kg for the first cycle and becomes more constant at 2.06 Wh/kg beyond the first cycle, meaning that a similar energy barrier is seen by cations and anions when they transport to the surface of the electrodes for the cycles. The E has a similar pattern to that of the C in Figure 13. The slight decrease in E through the cycles is due to the increase of ESR, and thus the energy loss increases through the mechanism of charging-discharging cycles [78,83]. The P value measured in this work is shown in Figure 15. The P shows a slight drop beyond the 100th cycle within charge-discharge for 450 cycles, and this might be due to the electrolyte depletion. Ion agglomerations after the swift charge and discharge mechanism block the transportation of ions to the electrode surface, and thus the ion adsorption decreases at the electrode-electrolyte interfaces [84]. Table 6 indicates the comparison of the P and E of the EDLC with those of previous reports. Shim et al. [85] developed a dual anion-doped PVA gel electrolyte with Methanesulfonic acid (MSA) as a multi-functional additive to improve the electrochemical performance and wearability of quasi-solid-state fiber-shaped Zn-polyaniline batteries (Fs-ZPBs). The MSA-based Fs-ZPB revealed a great rate capability, showing long cycling stability (capacity retention = 88.1% after 2000 cycles), a specific capacity of 100.3 mAh g−1 at 5 A g−1, and high power and energy densities of 9135.4 W kg−1 and 115.4 Wh kg−1, respectively. Furthermore, the prepared Fs-ZPBs showed high flexibility with a capacity retention of 92.7% after 500 cycles at a bending radius of 2.5 mm [85].

Figure 14

Energy density of the EDLC device for the 450 cycles at RT.

Figure 15

Power density of the EDLC device for the 450 cycles at RT.

4. Conclusions

PVA/NH4SCN/glycerol-based electrolytes were formed by the solution casting method. Using FTIR, the interaction of the elements of the electrolyte was established at 40 wt. % glycerol. The 40 wt. % glycerol addition increased the DC conductivity to 1.82 × 10−5 S cm−1. It was shown that when the glycerol increased, the number density (n), mobility (μ), and diffusion coefficient (D) of the ions improved. It was shown by the FESEM that the PSP_2 has a smooth surface morphology. The conductivity trend was further verified by dielectric examination. TNM showed that the majority of carriers were cations and anions, and the tion and te for the PSP_2 were measured to be 0.902 and 0.097, respectively. LSV showed that the SEW for the PSP_2 was at 1.99 V, showing the eligibility of the SPE in the EDLC application. The profile of CV indicates a rectangle with the absence of redox peaks, which confirms the ELDC capacitive behavior. The Cd, Ed, and Pd obtained for the EDLC were 18.3 F g−1, 2.06 Wh/kg, and 318.73 W/kg, respectively. The ESR of the EDLC throughout 450 cycles varied from 245 to 278 Ω.