1.8 V Aqueous Symmetric Carbon-Based Supercapacitors with Agarose-Bound Activated Carbons in an Acidic Electrolyte.
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ABSTRACT:
SUBMITTER: Lai CC
PROVIDER: S-EPMC8308127 | biostudies-literature |
REPOSITORIES: biostudies-literature
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Project description:Aqueous symmetric carbon-based supercapacitors (CSCs) are always the research focus for energy storage devices because of the virtue of low cost, inherent safety, and encouraging electrochemical stability. As is well-known, so far most aqueous symmetric CSCs are subjected to low energy densities. Here, a symmetric supercapacitor comprising electrodes from biomass-derived activated carbon and alkaline-acidic electrolyte is reported. This aqueous symmetric CSC demonstrates exceptional electrochemical performance with high stable working voltage of 2 V and attractive cycling stability of no capacitance loss over 10 000 cycles. Impressively, it shows a remarkable energy density of 36.9 W h kg-1 at 248 W kg-1 based on the total mass of the active materials, which is much higher than traditional aqueous symmetric CSCs, and a power density of 4083 W kg-1 with an energy density of 8.8 W h kg-1. The use of stable alkaline-acidic electrolyte provides an innovative technique to enhance the energy density of aqueous supercapacitors.
| S-EPMC6325591 | biostudies-literature
Project description:The synthesis of biomass-derived porous carbons (PCs) for supercapacitors by conventional two-steps method (chemical activation after carbonization) is complicated and time-consuming. In this study, we present a one-step microwave activation strategy to prepare hierarchically PCs from waste palm boosted by activated carbons (ACs). ACs with various specific surface areas (14, 642, and 1344 m²·g-1) were used for the first time to fast absorb microwave energy for converting waste palm into hierarchically PCs, that is, PC1, PC2, and PC3, respectively. The morphological and structural characterizations of PCs were studied. Also, the electrochemical performances of supercapacitors based on PCs as electrodes were further investigated. The results showed that the PC (PC1) boosted by AC with the lowest specific surface area possessed a porous structure (containing micro-, meso-, and macro- pores) with the largest specific surface area (1573 m²·g-1) and the highest micropore volume (0.573 cm³·g-1), as well as the suitable mesoporosity (29.69%). The as-prepared PC1 supercapacitor even in a gel electrolyte (PVA/LiCl) exhibited a high specific capacitance of 226.0 F·g-1 at 0.5 A·g-1 and presented excellent charge-discharge performance with an energy density of 72.3 Wh·kg-1 at a power density of 1.4 kW·kg-1 and 50.0 Wh·kg-1 at 28.8 kW·kg-1. Moreover, this promising method exhibited a simple, rapid, and cost-effective preparation of carbon materials from renewable biomass for energy storage applications.
| S-EPMC6473988 | biostudies-literature
Project description:The recyclable utilization of waste biomass is increasingly important for the development of a sustainable society. Here, the sawdust-derived activated carbon (SD-AC) has been prepared via a convenient H3PO4-based activation method and further trialed as an electrode for use as a high-performance symmetric supercapacitor. The as-prepared SD-AC possesses a hierarchically porous structure with micropores (0.55 nm) and mesopores (2.58 nm), accounting for its high specific surface area of 621 m2 g-1, with a pore volume of 0.35 cm3 g-1. Such a hierarchically porous structure can offer a favorable pathway for fast ion penetration and transportation, enhancing its electrochemical performance. As a result, the SD-AC electrode exhibits a maximum specific capacitance of up to 244.1 F g-1 at 1.0 A g-1, a high rate capability (129.06 F g-1 at 20 A g-1), and an excellent cycling performance, with 87% retention over 10,000 cycles at 10 A g-1. Of particular note is that the SD-AC-based symmetric supercapacitor achieves a maximum energy density of 19.9 Wh kg-1 at the power density of 650 W kg-1, with a long-term cycle lifespan. This work showcases the recyclable utilization of waste biomass for the preparation of high-value activated carbon for efficient energy storage.
| S-EPMC8912637 | biostudies-literature
Project description:Supercapacitors are increasingly in demand among energy storage devices. Due to their abundant porosity and low cost, activated carbons are the most promising electrode materials and have been commercialized in supercapacitors for many years. However, their low packing density leads to an unsatisfactory volumetric performance, which is a big obstacle for their practical use where a high volumetric energy density is necessary. Inspired by the dense structure of irregular pomegranate grains, a simple yet effective approach to pack activated carbons into a compact graphene network with graphene as the "peels" is reported here. The capillary shrinkage of the graphene network sharply reduces the voids between the activated carbon particles through the microcosmic rearrangement while retaining their inner porosity. As a result, the electrode density increases from 0.41 to 0.76 g cm-3. When used as additive-free electrodes for supercapacitors in an ionic liquid electrolyte, this porous yet dense electrode delivers a volumetric capacitance of up to 138 F cm-3, achieving high gravimetric and volumetric energy densities of 101 Wh kg-1 and 77 Wh L-1, respectively. Such a graphene-assisted densification strategy can be extended to the densification of other carbon or noncarbon particles for energy devices requiring a high volumetric performance.
| S-EPMC6661934 | biostudies-literature
Project description:Here, we present a facile and low-cost method to produce hierarchically porous graphene-based carbons from a biomass source. Three-dimensional (3D) graphene-based carbons were produced through continuous sequential steps such as the formation and transformation of glucose-based polymers into 3D foam-like structures and their subsequent carbonization to form the corresponding macroporous carbons with thin graphene-based carbon walls of macropores and intersectional carbon skeletons. Physical and chemical activation was then performed on this carbon to create micro- and meso-pores, thereby producing hierarchically porous biomass-derived graphene-based carbons with a high Brunauer-Emmett-Teller specific surface area of 3,657?m2?g-1. Owing to its exceptionally high surface area, interconnected hierarchical pore networks, and a high degree of graphitization, this carbon exhibited a high specific capacitance of 175?F?g-1 in ionic liquid electrolyte. A supercapacitor constructed with this carbon yielded a maximum energy density of 74?Wh?kg-1 and a maximum power density of 408?kW?kg-1, based on the total mass of electrodes, which is comparable to those of the state-of-the-art graphene-based carbons. This approach holds promise for the low-cost and readily scalable production of high performance electrode materials for supercapacitors.
| S-EPMC5789836 | biostudies-other
Project description:Amongst the materials being investigated for supercapacitor electrodes, carbon based materials are most investigated. However, pure carbon materials suffer from inherent physical processes which limit the maximum specific energy and power that can be achieved in an energy storage device. Therefore, use of carbon-based composites with suitable nano-materials is attaining prominence. The synergistic effect between the pseudocapacitive nanomaterials (high specific energy) and carbon (high specific power) is expected to deliver the desired improvements. We report the fabrication of high capacitance asymmetric supercapacitor based on electrodes of composites of SnO2 and V2O5 with multiwall carbon nanotubes and neutral 0.5 M Li2SO4 aqueous electrolyte. The advantages of the fabricated asymmetric supercapacitors are compared with the results published in the literature. The widened operating voltage window is due to the higher over-potential of electrolyte decomposition and a large difference in the work functions of the used metal oxides. The charge balanced device returns the specific capacitance of ~198 F g(-1) with corresponding specific energy of ~89 Wh kg(-1) at 1 A g(-1). The proposed composite systems have shown great potential in fabricating high performance supercapacitors.
| S-EPMC4616038 | biostudies-literature
Project description:Facing the increasing demand for various renewable energy storage devices and wearable and portable energy storage systems, the research on electrode materials with low costs and high energy densities has attracted great attention. Herein, free-standing rGO-CNT nanocomposites have been successfully synthesized by a facile hydrothermal method, in which the hierarchical porous network nanostructure is synergistically assembled by rGO nanosheets and CNT with interlaced network distribution. The rGO-CNT composite electrodes with synergistic enhancement of rGO and CNT exhibit high specific capacitance, excellent rate capability, exceptional conductivity and outstanding long-term cycling stability, especially for the optimal rGO-CNT30 electrode. Applied to a symmetric supercapacitor systems (SSS) assembled with an rGO-CNT30 electrode and with 1 M Na2SO4 aqueous solution as the electrolyte, the SSS possesses a high energy density of 12.29 W h kg-1 and an outstanding cycling stability, with 91.42% of initial specific capacitance after 18,000 cycles. Results from these electrochemical properties suggest that the rGO-CNT30 nanocomposite electrode is a promising candidate for the development of flexible and lightweight high-performance supercapacitors.
| S-EPMC8229913 | biostudies-literature
Project description:PurposePer- and polyfluoroalkyl substances (PFAS) have been found to be widespread, extremely persistent and bioaccumulative with toxicity tendencies. Pre-synthesized nanocomposite-activated carbons, referred to, as physically activated maize tassel silver (PAMTAg) and chemically activated maize tassel silver (CAMTAg) were utilized in the present study. They were used for the removal of 10 PFAS from aqueous solutions.MethodsThe nanocomposite-activated carbons were characterized via scanning electron microscopy (SEM), Fourier transform infrared (FTIR) spectroscopy, Brunauer Emmett Teller (BET) and other techniques. Batch equilibrium experiments were conducted in order to investigate the effects of solution pH, adsorbent dosage, initial PFAS concentration and temperature on the removal of PFAS using PAMTAg and CAMTAg. Langmuir and Freundlich adsorption isotherm models were used to analyse the equilibrium data obtained.ResultsMaximum adsorption capacities of 454.1 mg/g (0.91 mmol/g) and 321.2 mg/g (0.78 mmol/g) were recorded for perfluorooctanesulfonate (PFOS) and perfluorooctanoate (PFOA), respectively using CAMTAg. The values recorded for the Gibbs' free energy (ΔG°) for the adsorption of PFOS and PFOA onto PAMTAg and CAMTAg were negative; PFOS (-9.61, -9.99 and - 10.39), PFOA (-8.77, -9.76 and - 10.21) using PAMTAg; and PFOS (-13.70, -12.70 and - 12.37), PFOA (-12.86, -12.21 and - 11.17) using CAMTAg. Therefore, the adsorption processes were spontaneous and feasible. The values recorded for enthalpy (ΔH°) (kJ/mol) for the adsorption of PFOS (-26.15) and PFOA (-35.86) onto CAMTAg were negative, indicating that the adsorption mechanism is exothermic in nature. Positive values were recorded for ΔH° for the adsorption of PFOS (2.32) and PFOA (12.69) onto PAMTAg, indicative of an endothermic adsorption mechanism. Positive entropy (ΔS°) values (0.04 and 0.07) were recorded for PFOS and PFOA using PAMTAg; whereas negative values (-0.04 and - 0.08) were recorded for ΔS° using CAMTAg. A positive ΔS° indicates an increase in randomness of the adsorbate at the solid-solution interface and the reverse is the case for a negative ΔS°.ConclusionThe interplay of electrostatic attraction and hydrophobic interactions enabled the removal of PFAS using PAMTAg and CAMTAg. Findings suggest that PAMTAg and CAMTAg are effective for the removal of PFAS from aqueous media and are good alternatives to commercially available activated carbons.Graphical abstractSupplementary informationThe online version contains supplementary material available at 10.1007/s40201-020-00597-3.
| S-EPMC8172664 | biostudies-literature
Project description:Rational design and development of the electrodes with high-mass loading yet maintaining the excellent electrochemical properties are significant for a variety of electrochemical energy storage applications. In comparison with the slurry-casted electrode, herein, a hierarchically porous activated carbon (HPAC) electrode with higher mass loading (8.3 ± 0.2 mg/cm2) is successfully prepared. The pouch-type symmetric device (1 cell) with the propylene carbonate-based electrolyte shows the rate capability (7.1 F at 1 mA/cm2 and 4.8 F at 10 mA/cm2) and the cycling stability (83% at 12,000 cycles). On the other hand, an initial discharge capacitance of 32.4 F and the capacitance retention of 96% after 30,000 cycles are delivered from a pouch-type symmetric supercapacitor (five cells). The corresponding electrochemical performances are attributed to the fascinating properties of the HPAC and the synergistic features of the resulting electrode.
| S-EPMC8003487 | biostudies-literature
Project description:Easy regenerability of core components such as electrode and electrolyte is highly required in advanced electrochemical devices. This work reports a reliable, regenerable, and stretchable hydrogel electrolyte based on ionic bonds between polyacrylic acid (PAA) and polyallylamine (PAH). PAA-PAH electrolyte (1M LiCl addition) exhibits high ionic conductivity (0.050 S·cm-1) and excellent mechanical property (fracture strain of 1,688%). Notably, the electrolyte can be regenerated to any desired shape under mild conditions and remains 96% and 90% of the initial ionic conductivity after the first and second regeneration, respectively. PAA-PAH/LiCl-based supercapacitor exhibits nearly 100% capacitance retention upon rolling, stretching, and 5,000 charge-discharge cycles, whereas the regenerated device holds 97.6% capacitance of the initial device and 90.9% after 5,000 cycles. This low-cost, high-efficiency, and regenerable hydrogel electrolyte reveals very promising use in solid-state/flexible supercapacitors and possibly becomes a standard commercial hydrogel electrolyte for sustainable electrochemical energy devices.
| S-EPMC7490843 | biostudies-literature