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International Journal of Electrochemistry
Volume 2011 (2011), Article ID 397685, 10 pages
The Capacitive Behaviors of Manganese Dioxide Thin-Film Electrochemical Capacitor Prototypes
Department of Chemistry, Faculty of Resource Science and Technology, Universiti Malaysia Sarawak, Kota Samarahan 94300, Sarawak, Malaysia
Received 31 May 2011; Revised 21 July 2011; Accepted 18 August 2011
Academic Editor: Kenneth I. Ozoemena
Copyright © 2011 Suh Cem Pang et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
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 thin-film electrochemical capacitors have high potential utility as pulsed power sources, as well as load-leveling functions in various consumer electronic devices.
The phenomenal increase in demands for electronic devices, power tools, and energy-intensive device applications necessitate the continual development of new generation energy-storage 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- (MnO2-) based electrodes have been reported to exhibit high specific capacitance which ranged from 130 to 700 F/g in mild aqueous electrolytes [1–3]. However, these capacitance values are still substantially lower than the theoretical value of 1,380 F/g which corresponds to the complete reduction of Mn4+ to Mn3+. Low utilization of bulk MnO2 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 . 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 MnO2 of nanofibers [5, 6], nanowires , sea urchin-like and clew-like shapes , carambola-like nanoflakes , and nanorods  have been synthesized by various approaches. However, none of these nanostructured MnO2 materials could achieve the level of electrochemical performances close to the theoretical specific capacitance value of MnO2.
The microstructure and surface morphology of MnO2 thin films are of particular interest since they influence the capacitive behaviors of MnO2 EC prototypes. This study has focused on elucidating factors that affect the capacitive behaviors of MnO2-based thin-film EC prototypes. Nanostructured MnO2 thin films were deposited directly onto nickel-coated poly(ethylene terephthalate) (Ni-PET) supporting substrate by the horizontal submersion deposition process without addition of any binder and conductive materials. The electrochemical properties of MnO2 thin-film EC prototypes in mild Na2SO4 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 MnO2 thin-film EC prototypes were reported.
A stable manganese dioxide (MnO2) sol was prepared based on method reported by Perez-Benito et al. . 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 (18.2 M.cm) to form 50 mL of homogenous dark brown MnO2 sol. MnO2 thin films of uniform thickness were deposited directly onto nickel-coated PET substrate using the horizontal submersion deposition process developed by our research group . In this deposition process, a horizontally mounted nickel-coated PET substrate was being submerged completely in a measured volume of MnO2 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 MnO2 thin films were heat treated at 200°C in air for one hour and then used to fabricate MnO2 thin-film EC prototypes of dual-planar configuration comprising interdigitated array (IDA) electrodes.
Well-dispersed MnO2 nanoparticles and deposited MnO2 thin films were characterized by a scanning electron microscope (SEM; JEOL JSM 6390LA) and a transmission electron microscope (TEM; JEOL JEM-1230). MnO2 EC prototypes in 0.2 M Na2SO4 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 software-driven potentiostat/galvanostat (PARSTAT 2263). Effects of experimental parameters such as CV scan rates, electrolyte composition, and concentration on the capacitive behaviors of MnO2 EC prototypes were investigated. The specific capacitances of MnO2 EC prototypes were determined from both cyclic voltammograms, Nyquist plots, and constant current discharge curves based on the following equations, respectively where is the mass of electroactive materials, is the scan potential window, and represents the instantaneous anodic charge at any given time where is the angular frequency, is the imaginary impedance, and impedances at both frequencies of 100 mHz and 10 mHz were used where is the discharge current density, is the discharge time, and is the potential difference before and after discharge. The total electroactive mass loading, , of the EC prototype was determined by atomic absorption spectroscopy (AAS) based on the stoichiometric formula weight of MnO2, at 86.94 g/mol.
3. Results and Discussion
3.1. Microstructural Characterization of MnO2 Thin Films
MnO2 sol synthesized in this study consisted of uniform-sized MnO2 nanoparticles (20–40 nm in diameter) with aggregated nanofibrillar structures radiating outwards from the centre of each nanoparticle (Figure 1(a) and inset). MnO2 nanoparticles were observed to aggregate into clusters initially, which subsequently reorganized into longitudinal bundles of particle clusters (Figures 1(b) and 1(c)). Alignment and association of these longitudinal bundles of loosely packed MnO2 nanoparticles led to the formation of MnO2 thin films with highly porous microstructure.
Pronounced changes were observed in the surface morphology of MnO2 thin-film electrodes after prolonged voltammetric cycling. Figures 2(a)–2(d) shows SEM micrographs of the cross-sectional edge of MnO2 thin-film electrode before and after voltammetric cycling. The heat-treated MnO2 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 petal-like macroporous morphology was observed (Figure 2(d)). Lin and Chen had reported MnO2-coated graphite electrodes of similar surface morphology, which was attributed to the dissolution and redeposition of amorphous MnOOH, an electrochemically active product of MnO2 . 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 . Wei et al. had proposed a more comprehensive mechanism involving the dissolution and redeposition of manganese ions which led to the formation of petal-shaped nanosheet microstructure of MnO2 electrode upon prolonged cycling . 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.
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 Mn4+ to Mn2+ whereas Mn2+ ions would be oxidized to MnO2 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 MnO2 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 MnO2 electrode . The penetration depth of electrolyte cations depends greatly on the porosity of the electrode matrix . Besides, such surface morphological transformation could lead to improved capacitive behaviors of MnO2 electrode due to reduction in the interparticle contact resistance and hence higher electrical conductivity.
Figure 3(a) shows the cyclic voltammograms (CVs) of MnO2 thin-film EC prototype in 0.2 M Na2SO4 aqueous electrolyte. MnO2 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 MnO2 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 . 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 MnO2-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 cycles. This could be attributed to the excellent phase stability and reversibility of MnO2 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 . As such, the contribution of double-layer capacitance was deemed negligible, and was therefore excluded in calculating total specific capacitance of MnO2 EC prototypes.
3.2. 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 MnO2 films resembled the “sand-rose-” like structure of MnO2 films synthesized by Beaudrouet et al. via the reduction of KMnO4 or NaMnO4 in acidic medium . The intercalation of cations into the bulk electroactive material was facilitated by MnO2 film of high specific surface area. The specific capacitance of MnO2 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 MnO2 thin film as shown in Figures 2(a)–2(d) and discussed in the preceding section. MnO2 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 . 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.
3.3. Electrochemical Impedance Spectroscopy (EIS)
Figure 4 shows the Nyquist plots of MnO2 EC prototype after different charge/discharge cycles and the proposed equivalent circuit model. The capacitive behavior of MnO2 EC prototype was represented by the almost vertical line at the low frequency region. Pronounced shift of impedance plots upon cycling was observed in the low frequency region indicating substantial reduction in the total impedance (summation of real and imaginary impedances) of EC prototypes. The total impedance or equivalent series resistance (ESR) of the EC prototype could be separated into constituent impedances such as electrolyte resistance, contact resistance between the nickel current collector and MnO2 electrode, contact resistance between MnO2 nanoparticles, and the intrinsic resistance of MnO2 electroactive material.
Figure 5 shows the impedance data of the MnO2 EC prototype which was being fitted to the equivalent circuit model . This model comprises basic electronic components such as , uncompensated electrolyte resistance, , charge-transfer resistance, , Warburg resistance, and CPE, constant phase element. Two additional electronic components, and were added for taking into account the formation of an ionically conductive passivative layer on the MnO2 electrode, as was commonly observed in battery electrodes .
The 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 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 to indicated excellent electrochemical stability of MnO2 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 . A similar equivalent circuit model has been reported by Xu et al.  to study the charge storage mechanism of manganese dioxide electrode in various neutral electrolytes .
Under the finite diffusion condition, the capacitive behavior was attributed to the accumulation of cations at the impermeable interface of the electrode . 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 frequency-dependent constant phase element (CPE). In the low-frequency region (10 mHz or below), the impedance phase shifted along the real impedance axis to almost /2 which was indicative of excellent capacitive behavior (Figure 4) . The frequency power, n, representing phase angle n*/2 was observed to be closed to one throughout the cycling, and thus further substantiated the outstanding capacitive behavior of the MnO2 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 MnO2 EC prototypes upon prolonged cycling could be attributed to the morphological transformation of MnO2 thin-film electrodes as discussed in the preceding sections.
3.4. Effect of Scan Rate
The effect of scan rates was investigated in order to elucidate the underlying charge-storage mechanisms of MnO2 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 MnO2 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 . Based on the proposed charge-storage mechanisms of MnO2 EC prototypes, the rate of intercalation/deintercalation of protons and/or cations into/out of the bulk MnO2 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 MnO2 matrix was reduced due to diminished interactions of cations with the MnO2 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 MnO2 thin film could be too small for cations to penetrate, especially for cations with some degree of solvation . According to Toupin et al. the faradaic reactions were confined to the surface of MnO2 films due to the limited rate of proton/cations diffusion into the bulk of the film. The high internal resistance of the MnO2 thin-film electrode could have also contributed towards the limiting rate of proton/cations diffusion into the MnO2 lattice [27, 28]. This could plausibly explain the low specific capacitance values of MnO2 thin films as compared to its theoretical value.
The rate of diffusion of protons/cations into the bulk of MnO2 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 MnO2-based EC prototypes. The observed inverse correlation could be attributed to the activation and concentration polarization at high scan rates . The higher the scan rate, the lower the diffusivity of protons/cations into the bulk of electroactive material. Henceforth, only the outer surface of MnO2 thin films would be utilized to generate pseudocapacitance .
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 MnO2 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 . 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 MnO2 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 MnO2 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].
3.5. 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 ZnCl2 electrolyte indicating the excellent capacitive behavior and high cycling reversibility of MnO2 EC prototypes. MnO2 EC prototypes were observed to exhibit a higher specific capacitance value of 354 F/g in (NH4)2SO4 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 ions which possessed higher proton diffusion and ionic conductivity . However, MnO2 EC prototypes in aqueous electrolyte containing ions showed lower cycling reversibility during electrochemical charge/discharge as evidenced by their CV curves of distorted rectangular shape . Aqueous electrolyte containing Zn2+ ions appeared to be unsuitable for MnO2 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 MnO2 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 MnO2 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 MnO2 EC prototypes in aqueous electrolyte containing Mg2+ ions exhibited the highest specific capacitance value. Since Mg2+ 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 . Neither the large ionic radius of hydrated Mg2+ ions nor its higher oxidation state as compared to other hydrated cations constituted the limiting factors for the charge/discharge rate . Although the highest specific capacitance value of EC prototypes was obtained in aqueous electrolyte containing Mg2+ 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 m2s/V in H2O) and their small ionic radii (9 Å) would enable rapid charging/discharging rate and higher specific capacitance. Unfortunately, few electrode materials (especially MnO2) are electrochemically inert in strong acidic electrolyte. Long-term cycling stability (>10,000 charge/discharge cycles) was reported for MnO2-based electrode in electrolytes containing sulphate-based salts only .
3.6. Effect of Electrolyte Concentration
The effect of Na2SO4 electrolyte concentration on the specific capacitance of MnO2 EC prototypes was studied. Figure 10(a) shows cyclic voltammograms of MnO2 EC prototypes in different Na2SO4 electrolyte concentrations between 0.025 and 1.000 M at a fixed scan rate of 50 mV/s. Specific capacitance values of MnO2 EC prototypes were observed to increase nonlinearly with increase in Na2SO4 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 MnO2 electroactive material . Figure 10(b) shows the relationship between specific capacitance and the cation concentration or cation activity, pNaa, which can be calculated by the following equation: where is activity coefficient and is the cation concentration. The activity coefficient, can be calculated according to the Debye-Hückel equation: where and are coefficients, which, in this case, and , is the ion charge, is the ionic strength, and 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 MnO2 versus the cation activity () was obtained (Figure 10(b)), indicating that the charging process of MnO2 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 MnO2 electrode [23, 37].
Both electrochemical impedance spectroscopy and cyclic voltammetry had provided complimentary information on the capacitive behaviors of the MnO2 thin-film EC prototypes in a mild aqueous electrolyte. The capacitive behaviors of MnO2 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 MnO2 thin-film electrodes. Though the capacitive behaviors of the MnO2 EC prototypes were affected by electrolyte cations of different solvated sphere sizes, no pronounced correlation between them was evidenced. The specific capacitance of MnO2 EC prototypes decreased with increased CV scan rates within the range of 10 mV/s to 300 mV/s. MnO2 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.
This paper was partially funded by Universiti Malaysia Sarawak (UNIMAS) through the award of a special fundamental research Grant 01(K03)/557/2005(56).
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