Electric Double Layer Capacitors Research Articles

Tetraethylammonium Perfluorobutanesulfonate as an Alternative Salt for Electric Double Layer Capacitors

AbstractThe utilization of tetraethylammonium perfluorobutane sulfonate as a promising alternative salt for electrolyte solutions in electrochemical double layer capacitors is introduced in this study. A thorough analysis of the physical and electrochemical characteristics of tetraethylammonium perfluorobutane sulfonate was conducted, including the assessment of its ionic conductivity, viscosity, and thermal behavior, using a 1 M solution in acetonitrile. Comparative assessments were made between the performance of this novel electrolyte and two well‐studied electrolytes: 1 M tetraethylammonium tetrafluoroborate and 1 M tetraethylammonium bis(trifluoromethanesulfonyl)imide in acetonitrile, focusing on electrochemical performance and long‐term stability. Furthermore, an investigation into the impact of tetraethylammonium perfluorobutane sulfonate on the anodic dissolution of aluminum current collectors was conducted. The results highlight the potential of tetraethylammonium perfluorobutane sulfonate as an effective replacement for bis(trifluoromethanesulfonyl)imide‐based electrolytes.

Electrochemical Performance of Supercapacitor Using Plasticised Corn Starch Polymer Electrolyte Incorporated with Lithium Iodide

An electrical double-layer capacitor (EDLC) is a supercapacitor type that offers higher energy density and capacitance than an electrolytic capacitor. EDLC bridges the energy or power gap between the batteries, fuel cells, and dielectric capacitors. Most EDLCs are fabricated using electrolytic solutions, many of which are highly corrosive, leading to heavy, bulky, and leaky devices. This research assembled an EDLC employing a plasticised solid polymer electrolyte based on lithium iodide (LiI) doped corn starch. Glycerol was used as the plasticiser. The fabricated EDLC was characterised using cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and galvanostatic charge-discharge (GCD) techniques. The specific capacitance obtained from EIS was 1.74 F g–1. By analysing the Nyquist plot obtained from EIS, charge transfer resistance (Rct) and equivalent series resistance (ESR) were determined. CV of the EDLC was carried out at various sweep rates. The highest specific capacitance of 4.66 F g–1 was obtained at a 50 mV s–1 sweep rate. The EDLC was charged and discharged ten times at 1 mA constant current. From GCD, the specific capacitance was found to be in the 4.36 – 5.57 F g-1 range. From these results, starch-LiI-glycerol showed potential as a candidate for electrolyte material for energy device applications.Keywords: Electrolyte, electrical double-layer capacitor, glycerol, lithium iodide, solid polymer, starch, specific capacitance

A Binary Ionogel Electrolyte for the Realization of an All Solid-State Electrical Double-Layer Capacitor Performing at Low Temperature.

Over the last years, solid-state electrolytes made of an ionic liquid (IL) confined in a solid (inorganic or polymer) matrix, also known as ionogels, have been proposed to solve the leakage problems occurring at high temperatures in classical electrical double-layer capacitors (EDLCs) with an organic electrolyte, and thereof improve the safety. However, making ionogel-based EDLCs perform with reasonable power at low temperature is still a major challenge due to the high melting point of the confined IL. To overcome these limitations, the present contribution discloses ionogel films prepared in a totally oxygen/moisture-free atmosphere by encapsulating 70 wt % of an equimolar mixture of 1-ethyl-3-methylimidazolium bis(fluorosulfonyl)imide and 1-ethyl-3-methylimidazolium tetrafluoroborate - [EMIm][BF4]0.5[FSI]0.5 - into a poly(vinylidene fluoride-co-hexafluoropropylene) (PVdF-HFP) network. The further called "binary ionogel" films demonstrated a high flexibility and a good ionic conductivity of 5.8 mS cm-1 at 20 °C. Contrary to the ionogels prepared from either [EMIm][FSI] or [EMIm][BF4], displaying melting at Tm=-16 °C and -7 °C, respectively, the crystallization of confined [EMIm][BF4]0.5[FSI]0.5 is quenched in the binary ionogel, which shows only a glass transition at -101 °C. This quenching enables an increased ionicity and ionic diffusion at the interface with the PVdF host network, leading the binary ionogel membrane to display higher ionic conductivity below -20 °C than the parent binary [EMIm][BF4]0.5[FSI]0.5 liquid. Laminate EDLCs were built with a 100 μm thick binary ionogel separator and electrodes made from a hierarchical micro-/mesoporous MgO-templated carbon containing a reasonable proportion of mesopores to enhance the mass transport of ions, especially at low temperature where the ionic diffusion noticeably decreases. The EDLCs operated up to 3.0 V with ideal EDL characteristics from -40 °C to room temperature. Their output specific energy under a discharge power of 1 kW kg-1 is ca. 4 times larger than with a cell implementing the same carbon electrodes together with the binary [EMIm][BF4]0.5[FSI]0.5 liquid. Hence, this binary ionogel electrolyte concept paves the road for developing safe and flexible solid-state energy storage devices operating at subambient temperatures in extreme environments.

Conducting Carbon Black Nano‐Filler Doped Polymer Electrolyte for Electrochemical Application

AbstractThis study provides a development of polymer electrolytes with an emphasis on their use in electrochemical devices. In present study we develop a new conducting carbon black (CB) powder dispersed into polyethylene oxide (PEO) polymer electrolyte using solution cast method. Various characterization techniques such as Impedance spectroscopy technique (EIS), Fourier transform infrared spectroscopy (FTIR), and Window stability (LSV) Linear sweep voltammetry has been studied in detail. The maximum ionic conductivity polymer electrolyte was at 0.05 wt%. of CB with σ value 1.20×10−5 S/cm. Finally the prepared CB dispersed polymer electrolyte using maximum conductivity sample is sandwiched between electrodes to fabricate an Electric double layer capacitor and Dye‐sensitized solar cell which show highest electrical capacity value of 68.5 F/gm at 5 mV/s respectively and 2.97 % efficiency shown by solar cell at 1 sun condition.

Pecan Shell-Derived Activated Carbon for High-Electrochemical Performance Supercapacitor Electrode.

Carbon nanomaterials-based electric double-layer capacitors (EDLCs) are reliable and appealing energy-storage systems offering high power density and long cycling stability. However, these energy storage devices are plagued with critical shortcomings, such as low specific capacitance, inefficient physical/chemical activation process, and self-discharge of electrode materials, hindering their future application. In this work, we use a self-activation process, an environmentally benign and low-cost process, to produce high-performance activated carbon (AC). Novel activated carbon from pecan shells (PS) was successfully synthesized through a single-step self-activation process, which combines the carbonization and activation processes. The as-synthesized pecan shell-derived activated carbon (PSAC) provides a high-porosity, low-resistance, and ordered pore structure with a specific pore volume of 0.744 cm3/g and BET surface area of 1554 m2/g. The supercapacitors fabricated from PSAC demonstrate a specific capacitance of 269 F/g at 2 A/g, excellent cycling stability over 15,000 cycles, and energy and power density of 37.4 Wh/kg and of 2.1 kW/kg, respectively. It is believed that the high-efficiency PSAC synthesized from the novel self-activation method could provide a practical route to environmentally friendly and easily scalable supercapacitors.

Investigation of ion desolvation in aqueous electrolyte with carbon electrode via electrochemical in-situ Raman

Energy storage is an essential means to stabilize the fluctuation of renewable energy generation. Based on desolvation of electrolyte ions, high density charge storage in nanoporous electrodes has attracted widespread attention. The mechanism of ion transport within nanopores is currently under exploration. In this work, electric double layer capacitor was established using porous carbon electrode. Electrolytes with different hydrated/desolvatd ion radii were selected. The ion desolvation process was observed indirectly and concisely by using electrochemical in situ Raman technique on the carbon electrode. It was found that for ion with bigger solvation shells, its Raman intensity fluctuated with the cell charging voltage, which was caused by the desolvation of electrolyte ions. The desolvated ion has a strong polarization effect on the electron cloud of carbon. The influence of electrolyte concentrations on desolvation was also explored. High concentration electrolyte exhibits greater increase in Raman peak intensity. Our approach provides a way to study the physical mechanism and interface behavior of ion desolvation in electrochemical devices.

Improved Capacitive Performance of High‐Voltage Electric Double‐Layer Capacitors by Electrolyte Optimization Using Hierarchically Porous Carbon Electrodes

Advancement of the voltage window with stringent safety concerns is an imperative strategy to enhance the energy densities and output power delivery of electrical double‐layer capacitors (EDLCs). Solid‐state, water‐in‐salt (WIS), and ionic liquid‐based electrolytes are attractive and ideal choices for high‐voltage EDLCs due to their superior voltage window, electrochemical performance, and predominant safety aspects. Mindful of this, the current report demonstrates the electrochemical performance of new nanoporous carbon electrodes derived from waste dry leaves of Swietenia macrophylla with a high specific surface area (SSA) (1834 m2 g−1) in polymer–gel, WIS, and ionic liquids‐based electrolytes. Symmetric EDLC devices are fabricated using polymer gel solid‐state (PVA–Na2SO4), ionic liquids (EMIMBF4), and WIS (21 m LiTFSI) electrolytes with the electrochemical stability windows of (ESW) 2, 2.5, and 2 V, respectively. The assembled devices with Na2SO4/PVA, EMIMBF4, and 21 m LiTFSI (WIS) electrolytes‐based devices exhibit high energy densities of 40, 31, and 25 Wh kg−1 at 0.5 A g−1 and good output power delivery of 5, 6.23, and 3 kW kg−1 at 5 A g−1 with better cyclability features. Self‐discharging studies and systematic evaluation of high‐voltage EDLCs offer a sustainable method to develop high‐performance aqueous and diverse electrolyte‐based supercapacitors.

Plasticised chitosan: Dextran polymer blend electrolyte for energy harvesting application: Tuning the ion transport and EDLC charge storage capacity through TiO2 dispersion

This study investigates the performance of biopolymer electrolytes based on chitosan and dextran for energy storage applications. The optimization of ion transport and performance of electric double-layer capacitors EDCL using these electrolytes, incorporating different concentrations of glycerol as a plasticizer and TiO2 as nanoparticles, is explored. Impedance measurements indicate a notable reduction in charge transfer resistance with the addition of TiO2. DC conductivity estimates from AC spectra plateau regions reach up to 5.6 × 10−4 S/cm. The electric bulk resistance Rb obtained from the Nyquist plots exhibits a substantial decrease with increasing plasticizer concentration, further enhanced by the addition of the nanoparticles. Specifically, Rb decreases from ∼20 kΩ to 287 Ω when glycerol concentration increases from 10 % to 40 % and further drops to 30 Ω with the introduction of TiO2. Specific capacitance obtained from cyclic voltammetry shows a notable increase as the scan rate decreases, indicating improved efficiency and stability of ion transport. The TiO2-enriched EDCL achieves 12.3 F/g specific capacitance at 20 mV/s scan rate, with high ion conductivity and extended electrochemical stability. These results suggest the great potential of plasticizer and TiO2 with biopolymers in improving the performance of energy storage systems.

Advances in Carbon Xerogels: Structural Optimization for Enhanced EDLC Performance.

This review explores the recent progress on carbon xerogels (CXs) and highlights their development and use as efficient electrodes in organic electric double-layer capacitors (EDLCs). In addition, this work examines how the adjustment of synthesis parameters, such as pH, polymerization duration, and the reactant-to-catalyst ratio, crucially affects the structure and electrochemical properties of xerogels. The adaptability of xerogels in terms of modification of their porosity and structure plays a vital role in the improvement of EDLC applications as it directly influences the interaction between electrolyte ions and the electrode surface, which is a key factor in determining EDLC performance. The review further discusses the substantial effects of chemical activation with KOH on the improvement of the porous structure and specific surface area, which leads to notable electrochemical enhancements. This structural control facilitates improvement in ion transport and storage, which are essential for efficient EDLC charge-discharge (C-D) cycles. Compared with commercial activated carbons for EDLC electrodes, CXs attract interest for their superior surface area, lower electrical resistance, and stable performance across diverse C-D rates, which underscore their promising potential in EDLC applications. This in-depth review not only summarizes the advancements in CX research but also highlights their potential to expand and improve EDLC applications and demonstrate the critical role of their tunable porosity and structure in the evolution of next-generation energy storage systems.

Study of dielectric and interfacial properties of functional biopolymer-based electrolyte with enhanced conductivity for energy storage application

This study investigates sodium (Na+) ion-conductive biopolymer blend electrolytes with glycerol as a plasticizer for energy storage. Through FTIR, impedance spectroscopy, transference number measurement (TNM), and linear sweep voltammetry (LSV), we identify an optimal film for electric double layer capacitor (EDLC) application. Glycerol induces notable changes in polymer-salt interaction, evidenced by FTIR band shifts reflecting increased free ions. Impedance measurements show reduced bulk resistance with optimal plasticizer content, emphasizing the system's suitability for energy storage. The system exhibits high real permittivity relative to imaginary at lower frequencies, attributing to glycerol's dielectric constant and small bulk resistance. Loss tangent (tanδ) and Argand plots reveal the dominant ion conduction mechanism. Electrochemical assessments support the suitability of the film for EDLC applications, featuring a favorable transference number (tion = 0.94) and high decomposition voltage (2.6V). Cyclic voltammetry (CV) curves demonstrate effective EDLC device design with significant capacitance adaptability across varying scan rates (5.946 F/g to 24.074 F/g).

Dual Doping of Sulfur and Nitrogen Induces Hierarchical Porous Carbon from Wastes Medical Masks for Supercapacitor Electrodes

Demand for battery and supercapacitor materials rapidly increases as energy storage deployments accelerate. Waste-based supercapacitors have become a point of interest to accommodate growing demand and awareness of environmentally friendly products. This work aims to examine how doping with sulfur and nitrogen affects the morphology and structure of porous carbon synthesized from waste medical masks and the electrochemical performances of the prepared electrodes. Nitrogen- and sulfur-doped porous carbon (a-C:NS) is successfully obtained by solvothermal and hydrothermal processes in an autoclave followed by chemical activation using potassium hydroxide (KOH) and a carbonization procedure. Sulfur- and nitrogen-doping increase the yield compared to the directly carbonized process of the waste medical mask. The a-C:NS sample has a porous feature, showing the presence of S, N, O, and dominant C elements and the formation of C-S and C-N bonds. The supercapacitor electrode prepared from a-C:NS shows an electric double layer capacitor (EDLC)-like characteristic with a high specific capacitance (CS) of 300 F/g at the scanning rate of 5 mV/s. This study shows a possible route to transform polypropylene waste into functional materials for supercapacitor electrodes.

Electrode wettability and capacitance of electrical double layer capacitor: a classical density functional theory study

We suggest a coarse-grained water model for use in classical density functional theory (cDFT) to describe aqueous inorganic salt solutions that act as working electrolytes in electrical double-layer capacitors (EDLCs) with electrodes comprising two face-to-face doped carbon monolayers. Focus of the cDFT calculations lies on the influence of solvent electrode wettability (SEW) on capacitance and energy storage behaviors, while also considering its interaction with factors like electrolyte bulk concentration, pore size, electrode voltage, and temperature. New phenomena are disclosed theoretically. Remarkably, this study challenges the traditional notion that energy storage is consistently boosted by enhancing the electrode’s ionophobicity. Contrarily, the SEW effect reduces energy storage below the standard aqueous electrochemical window voltage (around 1.2 V) and only enhances the energy storage as the voltage surpasses a certain threshold up to the optimal window voltage (2 V–2.5 V). Furthermore, a non-monotonic SEW effect on energy storage is demonstrated under appropriate conditions, shedding new light on the complex relationship between ionophobicity and energy storage. Moreover, the present coarse-grained water model enables the prediction of the experimentally observed inverse relationship between temperature and capacitance. In contrast, the widely used electrolyte primitive model predicts the existence of a maximum value. The decisive factor for the impact of SEW on capacitance and energy storage is identified as congestion within the electrode pore, while other factors contribute by affecting this congestion. The present research offers valuable insights, highlighting the significance of SEW in the innovative and strategic design of aqueous inorganic EDLC devices.

Electrodeposition of polyaniline on reduced graphene oxide/cotton yarn with tunable electrochemical performance for flexible textile supercapacitors

Graphene/cotton fibers show significant promise in wearable energy storage due to their low cost, porous structure, and exceptional integration ability into wearable systems. However, the eco-unfriendly reductants and standalone electric double-layer capacitor hindered their application. Herein, a green and rapid hydrothermal-electrodeposition method was proposed to fabricate polyaniline (PANI) decorated reduced graphene oxide (rGO)/cotton yarns without using any chemical reductants and oxidants. The PANI/rGO/cotton (PRC) yarn exhibited porous conductive network, structural controllability, and mechanical flexibility. Additionally, the PRC yarn electrode delivers a fast electron transport and ion migration, synergistic energy storage contribution, and a controllable capacitance (up to 81.2 mF cm−1 at 0.2 mA cm−1). The assembled yarn supercapacitor shows a good capacitance (19.8 mF cm−1 at 0.08 mA cm−1), excellent energy-power density (2.7 μWh cm−1 at 40 μW cm−1), and great capacitance retention. This green fabrication of PRC yarns brings new insights into the development of wearable energy storage.

Zinc-Carbon Battery Recycling for Investigating Carbon Materials for Supercapacitor Applications.

In this paper, carbon materials, including graphene nanosheets and carbon nanoparticles, were prepared from spent zinc-carbon batteries by the following two simple methods: electrochemical exfoliation and ultrasonication. Here, graphene nanosheets were synthesized by electrochemical exfoliation in 0.5 M H2SO4 by using a direct current power supply with two carbon rods from spent zinc-carbon batteries. Carbon nanoparticles were prepared by fast ultrasonication in a low-cost, green solution of DI water and ethanol. Graphene nanosheets in this study have high quality, large scale, and good electrochemical ability, while carbon nanoparticles have a unique nanosize and a good specific surface area. These carbon materials were applied for electrochemical measurements for supercapacitor studies and showed excellent stability at different temperatures. Moreover, electric double-layer capacitor devices based on graphene nanosheets and carbon nanoparticles were also used in electrochemical studies with strong stability and good electrochemical capability.

High Volumetric Energy Density Supercapacitor of Additive-Free Quantum Dot Hierarchical Nanopore Structure.

The high surface-area-to-volume ratio of colloidal quantum dots (QDs) positions them as promising materials for high-performance supercapacitor electrodes. However, the challenge lies in achieving a highly accessible surface area, while maintaining good electrical conductivity. An efficient supercapacitor demands a dense yet highly porous structure that facilitates efficient ion-surface interactions and supports fast charge mobility. Here we demonstrate the successful development of additive-free ultrahigh energy density electric double-layer capacitors based on quantum dot hierarchical nanopore (QDHN) structures. Lead sulfide QDs are assembled into QDHN structures that strike a balance between electrical conductivity and efficient ion diffusion by employing meticulous control over inter-QD distances without any additives. Using ionic liquid as the electrolyte, the high-voltage ultrathin-film microsupercapacitors achieve a remarkable combination of volumetric energy density (95.6 mWh cm-3) and power density (13.5 W cm-3). This achievement is attributed to the intrinsic capability of QDHN structures to accumulate charge carriers efficiently. These findings introduce innovative concepts for leveraging colloidal nanomaterials in the advancement of high-performance energy storage devices.

Metal oxide-based nanocomposites as advanced electrode materials for enhancing electrochemical performance of Supercapacitors: A comprehensive review

In recent years, the escalating use of nonrenewable fossil fuels has emerged as a significant threat to global sustainability, prompting the need for renewable, cost-effective, and eco-friendly energy storage solutions. Supercapacitors (SCs) are notable for their high power density (PD), cycle stability, and swift charge/discharge rates, although they fall short in energy density (ED) compared to traditional batteries. The performance of SCs is greatly influenced by the electrode materials used, highlighting the importance of material innovation in tackling the challenges posed by increasing fossil fuel consumption. Transition metal oxides (TMOs), known for their redox activity in energy storage, have been thoroughly investigated for their exceptional specific capacitance, which ranges from 100 to 2000F g−1, surpassing that of electrical double-layer capacitors (EDLCs). TMOs such as ruthenium oxide (RuO2), manganese oxide (MnO2), nickel oxide (NiO), cobalt oxide (Co3O4), tin oxide (SnO2), zinc oxide (ZnO), tungsten oxide (WO3), and vanadium pentoxide (V2O5) are widely researched for their high theoretical capacitance, affordability, and longevity. This review emphasizes the groundbreaking potential of metal oxide nanocomposites (NCs) formed by combining them with graphene, carbon nanotubes (CNTs), and polymers, leading to synergistic enhancements in electrical conductivity, surface area, and charge storage capacity. This thorough review not only presents an in-depth analysis of current research but also sheds light on potential future developments, contributing to the ongoing progress in the field of advanced electrode materials for energy storage.

Stroboscopic time-of-flight neutron diffraction in long pulsed magnetic fields

We present proof-of-principle experiments of stroboscopic time-of-flight (TOF) neutron diffraction in long pulsed magnetic fields. By utilizing electric double-layer capacitors, we developed a long pulsed magnet for neutron diffraction measurements, which generates pulsed magnetic fields with the full widths at half maximum of >102 ms. The field variation is slow enough to be approximated as a steady field within the time scale of a polychromatic neutron pulse passing through a sample placed in a distance of the order of 101 m from the neutron source. This enables us to efficiently explore the reciprocal space using a wide range of neutron wavelength in high magnetic fields. We applied this technique to investigate field-induced magnetic phases in the triangular lattice antiferromagnets CuFe1−xGaxO2 (x=0,0.035). Published by the American Physical Society 2024

Novel approach: Simultaneous application of ionic liquid doped polymer electrolyte in supercapacitor and dye-sensitized solar cells

The present study reports the synthesis, characterization, and application as energy devices of an ionic liquid blended polymer electrolyte film in which the host polymer polyvinyl alcohol (PVA) is mixed with low viscosity ionic liquid (IL) 1-ethyl-3-methylimidazolium thiocyanate. Various characterization tools have been used further to elaborate electrical, structural, and photoelectrochemical properties. X-ray diffraction (XRD) and polarized optical microscope (POM) affirm the reduction of crystallinity of polymer, while Fourier transform infrared spectroscopy (FTIR) shows complexation and composite nature. Electrochemical impedance spectroscopy shows an enhancement in ionic conductivity by IL doping, where the highest conductivity is achieved at 60 wt% of IL concentration with a conductivity value of 6.21 × 10⁻⁴ S/cm. The ionic transference number (tion) and electrochemical stability measurement show the film's predominantly ionic nature and a reasonable stability window. Using maximum conducting film sandwiched between electrodes, we have successfully fabricated two devices, i.e., an electrical double-layer capacitor (EDLC) and a dye-sensitized solar cell (DSSC). The fabricated EDLC capacitor shows a specific capacitance of 125 F/g, while DSSC shows an efficiency of 1.1 % at one sun condition.

Holistic Processing of Sawdust to Enable Sustainable Hybrid Li-Ion Capacitors

Activated carbon has long been recognized as a promising electrode material for energy storage devices. The extraordinarily high specific area makes it challenging to replace in supercapacitors since electrical double-layer capacitors need such surfaces but also porous networks to enable electrolyte penetration. As a raw material for synthesizing activated carbon, sawdust offers key benefits, such as its renewability, abundance, favorable physical attributes for energy storage, and a more environmentally friendly synthesis process compared to mined alternative sources. In this work, electrochemical characterization is carried out which highlights the critical role of pelletization in enhancing the capacitive performance of sawdust-derived activated carbon, in addition to the implicit handling and logistical benefits. Subsequently, a Li-ion capacitor is assembled with an organic solvent-based electrolyte, sawdust-derived activated carbon serving as the positive electrode, and an Al-based foil negative electrode, potentially combining high energy and power density materials into a hybrid device. Despite commendable electrochemical performance and the use of a sustainable waste-derived positive electrode with a commoditized negative electrode, challenges remain regarding the ability to mitigate the role of surface functional groups that are stabilized by bio-carbon thermal treatments. Nevertheless, this distinctive architecture holds promise as an alternative high-power energy storage technology for a future filled with renewable energy, electric vehicles, and portable electronic devices.

The NaClO4-water eutectic electrolyte for environmentally friendly electrical double-layer capacitors operating at low temperature

Herein, owing to its remarkable ionic conductivity, the 8.84 mol kg−1 NaClO4 water-in-salt (WIS) eutectic electrolyte is suggested for the low temperature operation of electrical double-layer capacitors down to -35 °C. Molecular dynamic simulations reveal that the local structure of the solution remains relatively stable from RT to -35 °C, with distinct channel-like domains formed by hydrogen-bonded water molecules, which facilitate the ionic diffusion within the bulk of the electrolyte. Interestingly, on activated carbon (AC) electrodes, the electrolyte demonstrates an electrochemical stability window (ESW) increasing from 1.8 V to 2.1 V as temperature decreases from 25 °C to -35 °C. The high ESW of this electrolyte is due to i) pH close to neutrality enabling high overpotential of water reduction on porous AC electrodes; ii) WIS characteristics with a reduced amount of free water in the Stern layer under positive polarization of AC; iii) higher oxidation potential at low temperature ascribed to the enhanced immobilization of the ClO4− anions in the Stern layer as well as reduced diffusion of water molecules in the AC electrode porosity. The electrochemical investigations on laminate AC//AC cells in the NaClO4-water electrolyte demonstrate low values of their resistive components down to -30 °C, while the devices can operate with rated voltage of 2.0 V and 1.7 V at -30 °C and RT, respectively. At -30 °C and under discharge power as high as 10 kW kg−1, the AC//AC capacitor in the NaClO4-water electrolyte outperforms the specific output energy of a traditional AC//AC cell in the 1 M TEABF4/ACN electrolyte. Hence, for sub-ambient temperatures, the presented environmentally friendly EDLC holds promise to compete with traditional devices implementing an organic electrolyte.