Abstract:Abstract.-In order to understand the participation of electrical double layer and pseudocapacitance to the overall behavior of supercapacitors, a new approach to the analysis of the electrochemical data is proposed. Both the variation of the specific capacitance values and the dependence of these values with the operating voltage window (varying from 0-0.2 V to 0-1 V) were evaluated and used to quantify the contribution arising from each mechanism of energy storage to the total capacitance of the system. The s… Show more
“…The cell was able to store 80, 75, 70 and 64 F g À1 at 0.8, 1.0, 1.6 and 2.0 V, respectively, at the second cycle. According to Ruiz and colleagues [56], CV is inadequate to quantitatively isolate the contributions of double layer and pseudocapacitance in carbon based EDLC. Thus, galvanostatic charge-discharge (GCD) curves in Fig.…”
“…The cell was able to store 80, 75, 70 and 64 F g À1 at 0.8, 1.0, 1.6 and 2.0 V, respectively, at the second cycle. According to Ruiz and colleagues [56], CV is inadequate to quantitatively isolate the contributions of double layer and pseudocapacitance in carbon based EDLC. Thus, galvanostatic charge-discharge (GCD) curves in Fig.…”
“…As expected, limited double-layer charging is observed on the bare Pt electrode, indicating that the pseudocapacitive behavior observed on IFGO is a property of the hybrid material. already in previous reports [50,51]. Ruiz and co-workers did develop an empirical model in an attempt to decouple double-layer and pseudocapacitive contributions in carbon-based supercapacitor electrodes [51], but the general applicability of that method to our system is questionable.…”
“…already in previous reports [50,51]. Ruiz and co-workers did develop an empirical model in an attempt to decouple double-layer and pseudocapacitive contributions in carbon-based supercapacitor electrodes [51], but the general applicability of that method to our system is questionable. In our case, the double-layer formation is voltagedependent, as evidenced by the cyclic voltammograms of the unmodified GO and IFGO electrodes, likely a result of the microporous structure of the GO and IFGO composite sheets.…”
“…3B and 3D it can be inferred that the operating cell voltage could be extended to at least 1.5 V. When the applied cell voltage is 1.0 V, the negative electrode is working at around 0.2 V versus the reference electrode (Fig. 3D), but it is well known that this activated carbon can work at much more negative potentials without provoking the hydrogen evolution reaction [17,36]. Consequently, it can be predicted that, if the operating cell voltage is increased, the positive electrode will remain within the potential of the Ce 3+ /Ce 4+ reactions, while the negative electrode will shift to more negative potentials.…”
The energy density of carbon based supercapacitors (CBSCs) was significantly increased by the addition of an inorganic redox species [Ce 2 (SO 4 ) 3 ] to an aqueous electrolyte (H 2 SO 4 ). The development of the faradaic processes on the positive electrode not only significantly increased the capacitance but also the operational cell voltage of these devices (up to 1.5 V) due to the high redox potentials at which the Ce 3+ /Ce 4+ reactions occur. Therefore, in asymmetric CBSCs assembled using an activated carbon as negative electrode and MWCNTs as the positive one, the addition of Ce 2 (SO 4 ) 3 moderately increases the energy density of the device (from 1.24 W h kg -1 to 5.08 W h kg -1 ). When a modified graphite felt is used as positive electrode the energy density of the cell reaches values as high as 13.84 W h kg -1 . The resultant systems become asymmetric hybrid devices where energy is stored due to double layer formation in the negative electrode and the development of the faradaic process in the positive electrode, which acts as a battery-type electrode.
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