The Capacitive Behaviors of Manganese Dioxide Thin-Film Electrochemical Capacitor Prototypes

We have documented the fabrication of manganese dioxide (MnO2) thin-film electrochemical capacitor (EC) prototypes with dual-planar electrode configuration. These EC prototypes exhibited good capacitive behaviors in mild Na2SO4 aqueous electrolyte. Enhanced capacitive behaviors of EC prototypes were observed upon prolonged voltammetric cycling which could be associated with microstructural transformation of MnO2 thin-film electrodes from densely packed plate-like to irregular petal-like surface morphology. Effects of voltammetric scan rates, prolonged voltammetric cycling, electrolyte composition, and electrolyte concentration on the surface morphology of MnO2 thin-film electrodes, and associated capacitive behaviors of MnO2 thin-film EC prototypes were investigated by cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and galvanostatic charge/discharge (GCD) techniques. Results of both CV and EIS indicated that thin-film MnO2 EC prototypes exhibited the highest specific capacitance of 327 F/g in 0.2 M Na2SO4 aqueous electrolyte. Being environmentally benign and cheap, MnO2 thinfilm electrochemical capacitors have high potential utility as pulsed power sources, as well as load-leveling functions in various consumer electronic devices.


Introduction
The phenomenal increase in demands for electronic devices, power tools, and energy-intensive device applications necessitate the continual development of new generation energystorage systems of high rate capability and performances.Energy-storage devices particularly pseudocapacitive electrochemical capacitors (ECs) fabricated using various nanoparticulate transition metal oxides have gained increasing interest among research scientists worldwide due to their high energy and power densities.Among them, manganese dioxide-(MnO 2 -) based electrodes have been reported to exhibit high specific capacitance which ranged from 130 to 700 F/g in mild aqueous electrolytes [1][2][3].However, these capacitance values are still substantially lower than the theoretical value of 1,380 F/g which corresponds to the complete reduction of Mn 4+ to Mn 3+ .Low utilization of bulk MnO 2 electroactive material for electrical energy storage could be mainly attributed to microstructural factors associated with the electroactive material concerned.As such, microstructural control at the nanoscale has been one of the major focuses in the development of novel electroactive materials that exhibit both high energy and power densities.Electroactive materials of desired pore size distribution, microstructure, composition, particles size, as well as electrochemically active functional groups could be precisely architectured at nanoscale dimension [4].However, the manufacturing of such electroactive materials required rigorous and expensive processing steps, and hence economically not feasible for commercial energy storage applications.To date, various types of electroactive materials such as nanostructured MnO 2 of nanofibers [5,6], nanowires [7], sea urchin-like and clew-like shapes [8], carambola-like nanoflakes [9], and nanorods [10] have been synthesized by various approaches.However, none of these nanostructured MnO 2 materials could achieve the level of electrochemical performances close to the theoretical specific capacitance value of MnO 2 .
The microstructure and surface morphology of MnO 2 thin films are of particular interest since they influence the International Journal of Electrochemistry capacitive behaviors of MnO 2 EC prototypes.This study has focused on elucidating factors that affect the capacitive behaviors of MnO 2 -based thin-film EC prototypes.Nanostructured MnO 2 thin films were deposited directly onto nickel-coated poly(ethylene terephthalate) (Ni-PET) supporting substrate by the horizontal submersion deposition proc-ess without addition of any binder and conductive materials.The electrochemical properties of MnO 2 thin-film EC prototypes in mild Na 2 SO 4 aqueous electrolyte were evaluated using various established electrochemical characterization techniques.The effect of voltammetric scan rates, prolonged cycling, electrolyte composition, and concentration on the capacitive behaviors of MnO 2 thin-film EC prototypes were reported.

Experimental
A stable manganese dioxide (MnO 2 ) sol was prepared based on method reported by Perez-Benito et al. [11].Typically, 5 mL of potassium permanganate (1.0 × 10 −1 M) and 10 mL of sodium thiosulfate (1.88 × 10 −2 M) were mixed in ultrapure water (18.2MΩ.cm) to form 50 mL of homogenous dark brown MnO 2 sol.MnO 2 thin films of uniform thickness were deposited directly onto nickel-coated PET substrate using the horizontal submersion deposition process developed by our research group [12].In this deposition process, a horizontally mounted nickel-coated PET substrate was being submerged completely in a measured volume of MnO 2 sol for a predetermined duration.The excess sol was then siphoned off and the deposited film on the substrate was air-dried at ambience temperature.This deposition process was repeated for the desired number of times in order to obtain different film thicknesses.Deposited MnO 2 thin films were heat treated at 200 • C in air for one hour and then used to fabricate MnO 2 thin-film EC prototypes of dualplanar configuration comprising interdigitated array (IDA) electrodes.
Well-dispersed MnO 2 nanoparticles and deposited MnO 2 thin films were characterized by a scanning electron microscope (SEM; JEOL JSM 6390LA) and a transmission electron microscope (TEM; JEOL JEM-1230).MnO 2 EC prototypes in 0.2 M Na 2 SO 4 aqueous electrolyte were characterized by cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and galvanostatic charge/discharge (GCD) which were operated on a computer interfaced and softwaredriven potentiostat/galvanostat (PARSTAT 2263).Effects of experimental parameters such as CV scan rates, electrolyte composition, and concentration on the capacitive behaviors of MnO 2 EC prototypes were investigated.The specific capacitances of MnO 2 EC prototypes were determined from both cyclic voltammograms, Nyquist plots, and constant current discharge curves based on the following equations, respectively where m is the mass of electroactive materials, ΔV is the scan potential window, and Iδt represents the instantaneous anodic charge at any given time where ω (= 2π f ) is the angular frequency, Z img is the imaginary impedance, and impedances at both frequencies of 100 mHz and 10 mHz were used where I is the discharge current density, t is the discharge time, and ΔV is the potential difference before and after discharge.The total electroactive mass loading, m, of the EC prototype was determined by atomic absorption spectroscopy (AAS) based on the stoichiometric formula weight of MnO 2 , at 86.94 g/mol.2(a)-2(d) shows SEM micrographs of the cross-sectional edge of MnO 2 thin-film electrode before and after voltammetric cycling.The heattreated MnO 2 thin-film electrode was observed initially to consist of densely packed block-like microstructure (Figure 2(a)).However, this densely packed microstructure was replaced by microsized spherical particles after 50 charge/discharge cycles.A magnified SEM micrograph of such a dispersed microsized spherical particles revealed very irregular and rough surface morphology (Figure 2(b), inset), which subsequently evolved into irregular petal-like structure (Figure 2(c), inset) upon cycling for 100 cycles.Upon further prolonged cycling, an interconnected petallike macroporous morphology was observed (Figure 2(d)).Lin and Chen had reported MnO 2 -coated graphite electrodes of similar surface morphology, which was attributed to the dissolution and redeposition of amorphous MnOOH, an electrochemically active product of MnO 2 [13].The porous microstructure is electrochemically favorable since it could provide substantially larger spatial clearance for electrode expansion and contraction during cycling, thereby preventing any physical degradation of electrode due to high internal stress [14].Wei   redeposition of manganese ions which led to the formation of petal-shaped nanosheet microstructure of MnO 2 electrode upon prolonged cycling [15].The morphological characteristics of the electroactive material could significantly affect the faradaic reactions associated with charge-transfer and/or cations/protons intercalation into the bulk phase of electroactive material.

Results and Discussion
During electrochemical characterization, the cathodic current generated for the scan cycle from +0.9 V to 0.0 V was attributed to the reduction of Mn 4+ to Mn 2+ whereas Mn 2+ ions would be oxidized to MnO 2 during the reverse scan cycle, and subsequently deposited as the petal-shaped surface morphology of the electrode.Since these pseudocapacitive reactions occurred almost exclusively at the outermost layer of the MnO 2 electrode, petal-shaped microstructures was formed initially on the surface of electrode, but gradually extended into the bulk phase of electroactive material upon prolonged voltammetric cycling.Instead of being confined to the first few nanometers of electrode surface, electroactive material of higher porosity should lead to enhanced utilization by facilitating faradaic reactions through intercalation of protons/electrolyte cations into the bulk phase of the MnO 2 electrode [16].The penetration depth of electrolyte cations depends greatly on the porosity of the electrode matrix [17].Besides, such surface morphological transformation could lead to improved capacitive behaviors of MnO 2 electrode due to reduction in the interparticle contact resistance and hence higher electrical conductivity.
Figure 3(a) shows the cyclic voltammograms (CVs) of MnO 2 thin-film EC prototype in 0.2 M Na 2 SO 4 aqueous electrolyte.MnO 2 thin-film EC prototypes exhibited good capacitive behaviors within the potential window of −0.9 V to +0.9 V at a scan rate of 50 mV/s, as evidenced by the near rectangular shape of CV curves.The specific capacitance of MnO 2 EC prototype, as determined by integrating the area of CV curve, was substantially larger than values reported for carbon-based systems of similar weight or volume [18].For carbon-based systems, charges are normally stored electrostatically at the electrolyte/electrode interfacial region, and is therefore dependent upon the total specific surface area of electroactive material being exposed to the electrolyte.In contrast, the capacitance of MnO 2 -based EC prototype arises from rapid and reversible faradaic reactions between electrolyte ions and the electroactive material.No redox peaks were discernible from these rectangular CV curves even after prolonged charge/discharge cycling for up to 300 International Journal of Electrochemistry cycles.This could be attributed to the excellent phase stability and reversibility of MnO 2 thin films.According to Conway, the capacitance of metal-oxide electrodes is mainly attributed to pseudocapacitance, and supplemented by approximately 5% or less of electrostatic double-layer capacitance [18].As such, the contribution of double-layer capacitance was deemed negligible, and was therefore excluded in calculating total specific capacitance of MnO 2 EC prototypes.

Cyclic Voltammetry (CV).
The integrated areas within the CV curves were observed to increase substantially after the morphological transformation from the initial agglomerated plate-like to interconnected petal-like porous morphology.This morphological characteristic of MnO 2 films resembled the "sand-rose-" like structure of MnO 2 films synthesized by Beaudrouet et al. via the reduction of KMnO 4 or NaMnO 4 in acidic medium [19].The intercalation of cations into the bulk electroactive material was facilitated by MnO 2 film of high specific surface area.The specific capacitance of MnO 2 thin-film EC prototypes was observed to increase substantially from 124 F/g to 230 F/g after 300 charge/discharge cycles (Figure 3(b)).The enhanced electrochemical performance associated with morphological changes could be attributed to increased surface-to-volume ratio of the MnO 2 thin film as shown in Figures 2(a)-2(d) and discussed in the preceding section.MnO 2 thin films of highly porosity and specific surface area would enable easy accessibility of cations and/or protons during charge/discharge cycles.The diffusion pathway could be significantly shortened for films of macroporous structure as compared to that of densely packed block-like structure [20].The lower specific capacitance observed during initial cycles prior to any morphological transformation could be attributed to limited cationic diffusion and/or low electrolyte penetration into the bulk of electrode material.the nickel current collector and MnO 2 electrode, contact resistance between MnO 2 nanoparticles, and the intrinsic resistance of MnO 2 electroactive material.

Electrochemical Impedance Spectroscopy (EIS)
Figure 5 shows the impedance data of the MnO 2 EC prototype which was being fitted to the equivalent cir- . This model comprises basic electronic components such as R Ω , uncompensated electrolyte resistance, R ct , charge-transfer resistance, R W , Warburg resistance, and CPE, constant phase element.Two additional electronic components, CPE l and R l were added for taking into account the formation of an ionically conductive passivative layer on the MnO 2 electrode, as was commonly observed in battery electrodes [21].
The R ct values obtained by simulating the experimental results using the equivalent circuit model were observed to be rather consistent throughout the charge/discharge cycles (Figure 6(a)).This is expected because charge transfer is not affected by the electrode morphology but is affected by the oxidation states of manganese and active hopping sites within the electrode [2,22].Likewise, the R w value which represented proton/cation diffusion was also quite consistent and varied slightly between 0.12 mΩ and 0.14 mΩ (Figure 6(a)).The consistent ratio of R ct to R w indicated   excellent electrochemical stability of MnO 2 thin films.The reversibility of redox reaction had been reported to increase with the amount of hydrates presence within the electroactive material by providing electrochemically facile sites for charge-transfer reaction and cation diffusion [22].A similar equivalent circuit model has been reported by Xu et al. [23] to study the charge storage mechanism of manganese dioxide electrode in various neutral electrolytes [23].
Under the finite diffusion condition, the capacitive behavior was attributed to the accumulation of cations at the impermeable interface of the electrode [24].Since the wide range of dispersion in pore sizes of electrode gave rise to nonideal capacitive behavior, the capacitance in the equivalent circuit model was represented by the frequencydependent constant phase element (CPE).In the lowfrequency region (10 mHz or below), the impedance phase shifted along the real impedance axis to almost π/2 which was indicative of excellent capacitive behavior (Figure 4) [24].The frequency power, n, representing phase angle n * π/2 was observed to be closed to one throughout the cycling, and thus further substantiated the outstanding capacitive behavior of the MnO 2 EC prototypes.As shown in Figure 6(b), the constant phase element was directly affected by the porosity or specific surface area of the electroactive materials and was observed to increase gradually with increasing number of charge/discharge cycles.The improved capacitive behaviors of the MnO 2 EC prototypes upon prolonged cycling could be attributed to the morphological transformation of MnO 2 thin-film electrodes as discussed in the preceding sections.

Effect of Scan Rate.
The effect of scan rates was investigated in order to elucidate the underlying charge-storage mechanisms of MnO 2 thin-film EC prototypes.The rate of cation diffusion into the bulk electroactive material could be controlled by applying different scan rates during the CV test.Figure 7 shows CV curves of MnO 2 thin-film EC prototypes at various scan rates between 10 mV/s and 300 mV/s.Our findings concurred with results reported by Roberts and Slade [25].Based on the proposed charge-storage mechanisms of MnO 2 EC prototypes, the rate of intercalation/ deintercalation of protons and/or cations into/out of the bulk MnO 2 thin films would be affected by the scan rate [2,26].As the scan rate was increased, a clear deviation from the rectangular CV curve was observed.At low scan rate, the diffusion controlled intercalation/deintercalation of cations could access almost all available pores, resulting in an almost rectangular CV curve which was indicative of an ideal capacitive behavior.As the scan rate was increased, a deviation from the rectangular shape of CV curve was observed (Figure 7).At high scan rate, the diffusion of cations into the MnO 2 matrix was reduced due to diminished interactions of cations with the MnO 2 electrode surface.
Nevertheless, a significant portion of the bulk electroactive material was shown to be inaccessible by cations even at a very low scan rate as the pore size of MnO 2 thin film could be too small for cations to penetrate, especially for cations with some degree of solvation [15].According to Toupin et al. the faradaic reactions were confined to the surface of MnO 2 films due to the limited rate of proton/cations diffusion into the bulk of the film.The high internal resistance of the MnO 2 thin-film electrode could have also contributed towards the limiting rate of proton/cations diffusion into the MnO 2 lattice [27,28].This could plausibly explain the low specific capacitance values of MnO 2 thin films as compared to its theoretical value.The rate of diffusion of protons/cations into the bulk of MnO 2 nanoparticulate matrix was observed to be inversely related to the scan rate, with diminution of specific capacitance as the scan rate was increased (Figure 8).Hence, plots of specific capacitance versus inverse of scan rate should provide a good representation of the electrochemical characteristics of MnO 2 -based EC prototypes.The observed inverse correlation could be attributed to the activation and concentration polarization at high scan rates [29].The higher the scan rate, the lower the diffusivity of protons/cations into the bulk of electroactive material.Henceforth, only the outer surface of MnO 2 thin films would be utilized to generate pseudocapacitance [30].
Table 1 shows the substantial decrease in specific capacitance values from 327 F/g to 119 F/g as determined by CV at scan rates of 10 mV/s and 300 mV/s, respectively.However, further decrease in the scan rate would lead to insignificant increase in the specific capacitance when the threshold level had been reached.Besides, the inherent thickness and microstructure of MnO 2 films could have impeded further penetration of protons or cations.The voltammetric charge on the outer surface of the electroactive material could be inferred by extrapolation of an expected linear correlation between the specific capacitance and the inverse of scan rate [30].Nevertheless, such a linear correlation was not obtained in the present study, and the extrapolated specific capacitance value at infinite scan rate was very small.This observation was in consonance with the proposed pseudocapacitive charge-storage mechanism due to faradaic reactions which were sensitive to diffusion phenomena of electroactive species into the bulk porous electrode materials [19,31].
All MnO 2 EC prototypes were further evaluated with electrochemical impedance spectroscopy (EIS) immediately after every CV test at various scan rates, as well as the galvanostatic charge/discharge (GCD) technique.Specific capacitance values of MnO 2 thin-film electrochemical capacitor prototypes as determined by various techniques are as shown in Table 1, and they are comparable under specific experimental conditions.Changes in specific capacitance values of EC prototypes as determined by EIS were negligible.On the contrary, specific capacitance values of EC prototypes as determined by CV were observed to decrease by about 63% when the scan rate was increased from 10 mV/s to 300 mV/s.These results further substantiated our earlier findings that a higher scan rate would significantly attenuate the capacitive performance of the EC prototypes.Our findings concurred with results reported by several previous studies, all of which had indicated logarithmic reduction of specific capacitance values with increment of scan rate [19,29,32,33].

Effect of Electrolytes.
Figure 9 shows the cyclic voltammograms of EC prototypes evaluated in different aqueous electrolytes at a scan rate of 50 mV/s.Near-rectangular shape of CV curves were observed for all electrolytes except for ZnCl 2 electrolyte indicating the excellent capacitive behavior and high cycling reversibility of MnO 2 EC prototypes.MnO 2 EC prototypes were observed to exhibit a higher specific capacitance value of 354 F/g in (NH 4 ) 2 SO 4 aqueous electrolyte as compared with prototypes in aqueous electrolytes containing alkaline cations such as Li + , Na + , and K + ions (253-325 F/g).This could be attributed to aqueous electrolyte containing nonmetallic cations such as NH 4 + ions which possessed higher proton diffusion and ionic conductivity [29].However, MnO 2 EC prototypes in aqueous electrolyte containing NH 4 + ions showed lower cycling reversibility during electrochemical charge/discharge as evidenced by their CV curves of distorted rectangular shape [29].Aqueous electrolyte containing Zn 2+ ions appeared to be unsuitable for MnO 2 EC prototypes as exemplified by the distorted CV curve of distinctive redox peaks at both anodic and cathodic scans.
Table 2 shows specific capacitances values of MnO 2 EC prototypes as determined from both CV curves and EIS plots, which were found to be in agreement with each other.No pronounced correlation between specific capacitance of MnO 2 EC prototype and different electrolyte cations was observed despite substantial differences in their hydration sphere radii.Results from both CV and EIS tests showed that MnO 2 EC prototypes in aqueous electrolyte containing Mg 2+ ions exhibited the highest specific capacitance value.Since Mg 2+ ions did not undergo intense solvation which would have led to larger Stokes radius, and consequently lower ionic mobility in the porous region of electrode material [34].Neither the large ionic radius of hydrated Mg 2+ ions nor its higher oxidation state as compared to other hydrated cations constituted the limiting factors for the charge/discharge rate [35].Although the highest specific capacitance value of EC prototypes was obtained in aqueous electrolyte containing Mg 2+ ions, a slightly distorted CV curve was observed due to redox reactions that occurred during both anodic and cathodic scans.
The presence of appropriate cationic species in the electrolyte is essential for optimizing the pseudocapacitive performances of EC prototypes based on intercalation/ deintercalation processes that occur at the electrolyte/ electrode interfacial region.Selection of cationic species in the electrolyte should take into account the size of cations and their hydration spheres, as well as the chemical compatibility between electrode material and electrolyte.For instance, the high mobility of protons (H + ) (36.24 × 10 −8 m 2 s/V in H 2 O) and their small ionic radii (9 Å) would enable rapid charging/discharging rate and higher specific capacitance.Unfortunately, few electrode materials (especially MnO 2 ) are electrochemically inert in strong acidic electrolyte.Long-term cycling stability (>10,000 charge/discharge cycles) was reported for MnO 2 -based electrode in electrolytes containing sulphate-based salts only [36].

Effect of Electrolyte Concentration.
The effect of Na 2 SO 4 electrolyte concentration on the specific capacitance of MnO 2 EC prototypes was studied.Figure 10(a) shows cyclic voltammograms of MnO 2 EC prototypes in different Na 2 SO 4 electrolyte concentrations between 0.025 and 1.000 M at a fixed scan rate of 50 mV/s.Specific capacitance values of MnO 2 EC prototypes were observed to increase nonlinearly with increase in Na 2 SO 4 electrolyte concentration.The highest specific capacitance value of approximately 200 F/g was obtained at electrolyte concentrations above 0.5 M. At high electrolyte concentration, the presence of excessive Na + ions could either saturate electroactive sites or hinder access into the bulk of MnO 2 electroactive material [28].Figure 10(b) shows the relationship between specific capacitance and the cation concentration or cation activity, pNa a , which can be calculated by the following equation: Cation activity, Na a = f i c, ( 4 ) where f i is activity coefficient and c is the cation concentration.The activity coefficient, f i can be calculated according to the Debye-Hückel equation: where A and B are coefficients, which, in this case, A = 0.5115 and B = 0.3291, z i is the ion charge, I is the ionic strength, and å is the hydrated ion size of the cation.The cation activity was used instead of cation concentration in order to reflect the actual cation concentration involved in the electrochemical reactions.A linear plot of the specific capacitance of MnO 2 versus the cation activity (R 2 = 0.96) was obtained (Figure 10(b)), indicating that the charging process of MnO 2 was a first-order reaction with respect to the cation activity with a slope of −11.46.The linear relationship implied that the charge/discharge process was mainly controlled by the intercalation/deintercalation of cations within the MnO 2 electrode [23,37].

Conclusions
Both electrochemical impedance spectroscopy and cyclic voltammetry had provided complimentary information on the capacitive behaviors of the MnO 2 thin-film EC prototypes in a mild aqueous electrolyte.The capacitive behaviors of MnO 2 thin-film EC prototypes were mainly attributed to the intercalation/deintercalation of protons and/or electrolyte cations into the electroactive material.The improved capacitive performance of the EC prototypes upon prolong charge/discharge cycling was associated with the morphological changes of MnO 2 thin-film electrodes.Though the capacitive behaviors of the MnO 2 EC prototypes were affected by electrolyte cations of different solvated sphere sizes, no pronounced correlation between them was evidenced.The specific capacitance of MnO 2 EC prototypes decreased with increased CV scan rates within the range of 10 mV/s to 300 mV/s.MnO 2 thin-film EC prototypes fabricated in this study exhibited the highest specific capacitance of 327 F/g at a slow CV scan rate of 10 mV/s.

Figure 3 :
Figure 3: (a) Cyclic voltammograms of MnO 2 thin-film EC prototypes evaluated in 0.2 M Na 2 SO 4 aqueous electrolyte cycled for up to 300 cycles, and (b) specific capacitance of MnO 2 thin-film EC prototypes (F/g) as a function of cycle number.

Figure 4 :Figure 5 :
Figure 4: (a) Equivalent circuit model of MnO 2 thin-film EC prototypes, (b) impedance plots of electrochemical capacitors (EC) at different charge/discharge cycle (inset shows the high-frequency regions of impedance plots).

Figure 6 :
Figure 6: (a) Charge-transfer and Warburg resistances, and (b) constant phase element (CPE) and frequency power (n), at different charge/discharge cycle.

Figure 7 :
Figure 7: Effect of scan rates on the shape of cyclic voltammograms.Only the 50th cycle of each cyclic voltammogram is shown.

Figure 8 :
Figure 8: The specific capacitance (F/g) of the MnO 2 thin-film EC prototypes versus the inverse of scan rate (1/scan rate).

Figure 9 :
Figure 9: Effect of electrolyte composition on the shape of cyclic voltammograms at a scan rate of 50 mV/s.Inset shows a magnified portion of various CV curves.

Figure 10 :
Figure 10: (a) Cyclic voltammograms in different Na 2 SO 4 electrolyte concentration at a scan rate of 50 mV/s, (b) specific capacitance (F/g) of the MnO 2 EC prototypes at different electrolyte concentration, [Na 2 SO 4 ], and cation activity, pNa a .
et al. had proposed a more comprehensive mechanism involving the dissolution and

Table 1 :
Specific capacitance (F/g) of MnO 2 thin-film electrochemical capacitor prototypes calculated from cyclic voltammograms (CVs) at different scan rates, and electrochemical impedance spectroscopy (EIS) at the frequency of 10 mHz.
a The scan rate was applicable for CV only.b EIS was conducted on the same electrode immediately after each CV test.c Galvanostatic charge/discharge conducted at a current density of 0.08 mA.

Table 2 :
Specific capacitance (F/g) of MnO 2 -based electrochemical capacitors in different aqueous electrolytes calculated from cyclic voltammograms (CVs) at scan rate of 50 mV/s and electrochemical impedance spectroscopy (EIS) at the frequency of 10 mHz.