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Power density vs. energy density plots at 2.7 V and at 3.2 V for electrochemical supercapacitors with ILs studied. Reproduced by permission of The Electrochemical Society from ref. 257.  

Power density vs. energy density plots at 2.7 V and at 3.2 V for electrochemical supercapacitors with ILs studied. Reproduced by permission of The Electrochemical Society from ref. 257.  

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Electrolytes have been identified as some of the most influential components in the performance of electrochemical supercapacitors (ESs), which include: electrical double-layer capacitors, pseudocapacitors and hybrid supercapacitors. This paper reviews recent progress in the research and development of ES electrolytes. The electrolytes are classifi...

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... The latter is higher for DMAc (0.89 mPa s vs. 0.33 mPa s for ACN) but similar to water (0.998 mPa s) and much lower than for propylene carbonate (2.4 mPa s), a widely used alternative for ACN in organic EDLCs. It is worth mentioning that the solvent's dielectric constant (ε) is inversely proportional to the interaction energy between ions with the opposite charge and, consequently, the ability of ion-pairs formation [35]. For the solvents with lower ε, the ion-pairing in the solution is privileged. ...
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The growing interest in hybrid (aqueous-organic) electrolytes for electrochemical energy storage is due to their wide stability window, improved safety, and ease of assembly that does not require a moisture-free atmosphere. When it comes to applications in electrochemical capacitors, hybrid electrolytes are expected to fill the gap between high-voltage organic systems and their high discharge rate aqueous counterparts. This article discusses the potential applicability of aqueous-organic electrolytes utilizing water/N,N-dimethylacetamide (DMAc) solvent mixture, and sodium perchlorate as a source of charge carriers. The hydrogen bond formation between H 2 O and DMAc (mole fraction x DMAc = 0.16) is shown to regulate the original water and cation solvation structure, thus reducing the electrochemical activity of the primary aqueous solution both in the hydrogen (HER) and oxygen (OER) evolution reactions region. As a result, an electrochemical stability window of 3.0 V can be achieved on titanium electrodes while providing reasonable ionic conductivity of 39 mS cm −1 along with the electrolyte's flame retardant and anti-freezing properties. Based on the diagnostic electrochemical studies, the operation conditions for carbon/carbon capacitors have been carefully optimized to adjust the potential ranges of the individual electrodes to the electrochemical stability region. The system with the appropriate electrode mass ratio (m + /m − = 1.51) was characterized by a wide operating voltage of 2.0 V, gravimetric energy of 13.2 Wh kg −1 , and practically a 100% capacitance retention after 10,000 charge-discharge cycles. This translates to a significant rise in the maximum energy of 76% when compared to the aqueous counterpart. Additionally, reasonable charge-discharge rates and antifreeze properties of the developed electrolyte enable application in a broad temperature range down to −20 • C, which is demonstrated as well.
... This allows for greater capacitance (more significant charge storage) than is feasible with ordinary capacitors. The main essential components of a SC include porous electrode material, current collector, separator, and electrolyte (6)(7)(8)(9). Recently, the materials utilized for these components have not been so environmentally friendly. ...
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... In contrast, an alternative subclass of supercapacitor, pseudo-capacitor, offers a route to store more charges than porous carbon through Faradaic reactions [4,5]. For example, common transition metal oxides [6][7][8] and conductive polymers [9,10] could theoretically provide specific capacity ranging from hundreds to over one thousand C g −1 via reversible surface redox reactions. However, low electrical conductivity and sluggish ion diffusion in the bulk active material have stifled power performance and limited the utilization of their theoretical storage capacity thus far [7,9]. ...
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... The graphite electrode (1x1 cm 2 area) was loaded with the resulting slurry with a dropper and placed in the oven to dry for 24 hr at 60 • C. After 24 hr, the graphite electrode containing slurry was immersed in aqueous 1 M H 2 SO 4 electrolytic solution [53,54]. All the studies of the samples were done in 1 M H 2 SO 4 electrolyte. ...
... ). nc/4.0/ -http://creativecommons.org/licenses/by ( The performance of the double electrolytic capacitor using them is not high [50]. Many studies conducted by recent researchers include that flexible supercapacitors, in which the electrolyte is in the solid state, have an important role in many applications, especially folding, because they are resistant to leakage, inexpensive, easy to pack, and have good mechanical stability. ...
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... In the present case, the rapid increase in peak current beyond 2.5 V is associated with the electrolyte decomposition, oxidation of the electrode surface, and evolution of gases at higher potentials. [74,75] The EIS plot of the device in the frequency range of 100 kHz to 100 mHz exhibited a small semicircle at higher frequencies (lower R ct ) and a linear response at lower frequencies attributed to the capacitive behavior of the electrode ( Figure S6). The GCD measurements were performed up to a 2 and 2.2 V voltage limit, as shown in Figure 4b, to evaluate the actual capacitance performance. ...
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... These methods generally help characterize the total solutes in solutions. Still, they cannot differentiate between the contributing ionic sources of these measurements-for example, the ionic conductivity of Na + (50.11 S cm 2 mol À1 ) versus Mg 2+ (106.12 S cm 2 mol À1 ; Zhong et al., 2015). Consequently, the reduction or loss of features critical to maintaining ecosystem integrity, such as biodiversity and microbe-mediated resource cycling, that are often attributed to the masking generic term 'salinization', may be more accurately described by an increase in a specific ionic component (Berger et al., 2019;Bogart et al., 2019;Cañedo-Argüelles et al., 2013;Clements & Kotalik, 2016;Griffith, 2014;Lo Nostro et al., 2005;Schuler & Relyea, 2018). ...
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The degradation of freshwater systems by salt pollution is a threat to global freshwater resources. Salinization is commonly identified by increased specific conductance (conductivity), a proxy for salt concentrations. However, conductivity fails to account for the diversity of salts entering freshwaters and the potential implications this has on microbial communities and functions. We tested 4 types of salt pollution—MgCl 2 , MgSO 4 , NaCl, and Na 2 SO 4 —on bacterial taxonomic and functional α‐, β‐diversity of communities originating from streams in two distinct localities (Nebraska [NE] and Ohio [OH], USA). Community responses depended on the site of origin, with NE and OH exhibiting more pronounced decreases in community diversity in response to Na 2 SO 4 and MgCl 2 than other salt amendments. A closer examination of taxonomic and functional diversity metrics suggests that core features of communities are more resistant to induced salt stress and that marginal features at both a population and functional level are more likely to exhibit significant structural shifts based on salt specificity. The lack of uniformity in community response highlights the need to consider the compositional complexities of salinization to accurately identify the ecological consequences of instances of salt pollution.
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Novel flake-like Ni1−xSnxO2 particles were successfully prepared by template-free hydrothermal synthesis. The prepared samples were investigated for their properties by different characterization techniques. Scanning micrographs showed that the obtained particles consisted of nanoflakes. The X-ray diffraction results of the Ni1−xSnxO2 revealed the formation of mixed-phase Ni/SnO2 having the typical tetragonal structure of SnO2, and the cubic structure of Ni in a nanocrystalline nature. The doping with Ni had a certain influence on the host’s lattice structure of SnO2 at different doping concentrations. Confirmation of the functional groups and the elements in the nanomaterials was accomplished using FTIR and EDS analyses. The electrochemical performance analysis of the prepared nanomaterials were carried out with the help of the CV, GCD, and EIS techniques. The specific capacitance of the synthesized nanomaterials with different concentrations of Ni dopant in SnO2 was analyzed at different scanning rates. Interestingly, a 5% Ni-doped SnO2 nanocomposite exhibited a maximum specific capacitance of 841.85 F g−1 at 5 mV s−1 in a 6 M KOH electrolyte. Further, to boost the electrochemical performance, a redox additive electrolyte was utilized, which exhibited a maximum specific capacitance of 2130.33 at 5 mV s−1 and an excellent capacitance retention of 93.22% after 10,000 GCD cycles. These excellent electrochemical characteristics suggest that the Ni/SnO2 nanocomposite could be utilized as an electrode material for high-performance supercapacitors.