All-solid-state supercapacitors using a highly-conductive neutral gum electrolyte

Recently, the development of safe, stable, and long-life supercapacitors has attracted considerable interest driven by the fast-growth of flexible wearable devices. Herein, we report an MnO₂-based symmetric all-solid-state supercapacitor, using a neutral gum electrolyte that was prepared by embedding aqueous sodium sulfate solution in a biopolymer xanthan gum. Resulting from the high ion conductivity 1.12 S m⁻¹, good water retention, and high structure adaption of such gum electrolyte, the presently described supercapacitor showed high electrochemical performance with a specific capacitance of 347 F g⁻¹ at 1 A g⁻¹ and an energy density of 24 μW h cm⁻² The flexible supercapacitor possesses excellent reliability and achieves a retaining capacitance of 82% after 5000 cycles. In addition, the as-prepared supercapacitor demonstrated outstanding electrochemical stability at temperatures between −15 °C to 100 °C.

A highly-conductive neutral gum electrolyte was used for all-solid-state supercapacitors with outstanding electrochemical performance at temperatures between −15 °C to 100 °C.     

N/O co-enriched graphene hydrogels as high-performance electrodes for aqueous symmetric supercapacitors

In this study, an easy one-pot hydrothermal strategy was used to prepare N/O co-enriched graphene hydrogels (NOGHs) using graphene oxide (GO) solution and n-propylamine as a reactant. The n-propylamine can be used not only as a reductant, nitrogen dopant and structure regulator, but also as a spacer to inhibit the agglomeration of graphene sheets. Benefiting from the synergistic effect between the heteroatoms (N, O), 3D porous structures and high specific surface area, the as-prepared NOGH samples present excellent electrochemical properties. Remarkably, the NOGH-140 based binder-free symmetric supercapacitor shows a high specific capacitance of 268.1 F g⁻¹ at the current density of 0.3 A g⁻¹ and retains 222.5 F g⁻¹ (82.9% of its initial value) at 10.0 A g⁻¹ in 6 M KOH electrolyte. Furthermore, the assembled device also displays a notable energy density (9.3 W h kg⁻¹) and outstanding cycling performance (1.8% increase of its initial specific capacitance after 10 000 cycles at 10 A g⁻¹). The simple preparation method and excellent electrochemical properties indicate that NOGHs can be used as electrode materials for commercial supercapacitors.

N/O co-enriched graphene hydrogel based supercapacitors were assembled. Owing to the synergistic effect between the heteroatoms (N, O), 3D porous structures and high specific surface area, they present excellent electrochemical properties.     

Cu-MOF derived Cu–C nanocomposites towards high performance electrochemical supercapacitors

For the development of asymmetric supercapacitors with higher energy density, the study of new electrode materials with high capacitance is a priority. Herein, the electrochemical behavior of nano copper in alkaline electrolyte is first discovered. It is found that there are two obvious reversible redox symmetric peaks in the range of −0.8–0.2 V in the alkaline electrolyte, corresponding to the conversion of copper into cuprous ions, and then converting cuprous ions into copper ions, indicating that the nanocomposite electrode has the characteristics of a pseudocapacitive reaction. It has a specific capacitance of up to 318 F g⁻¹ at a current density of 1 A g⁻¹, which remains at nearly 100% after 10 000 cycles at the same current density. When assembled with a Ni(OH)₂-based electrode into an asymmetric supercapacitor, the device shows excellent capacitive behavior and good reaction reversibility. At 0.4 A g⁻¹, the supercapacitor delivers a reversible capacity of 8.33 F g⁻¹ with an energy density of 13.5 mW h g⁻¹. This study first discovers the electrochemical behavior of nano copper, which can provide a new research idea for further expanding the negative electrodes of supercapacitors with higher energy density.

A new Cu–C nanocomposite derived from Cu-based metal–organic framework exhibits greatly improved electrochemical performance.     

N/S co-doped coal-based porous carbon spheres as electrode materials for high performance supercapacitors

N/S co-doped porous carbon spheres (NSPCSs) were prepared by a simple ultrasonic spray pyrolysis (USP) using the mixed solution of coal oxide and l-cysteine, and without a subsequent activation process. The surface properties of carbon materials have been successfully modified by the concurrent incorporation of N and S. So the capacitive performance of NSPCSs was greatly enhanced. It is used as a supercapacitor electrode to achieve a high specific capacitance of 308 F g⁻¹ at a current density of 1 A g⁻¹ and 90.2% capacitance retention even after 10 000 cycles at 5 A g⁻¹. These numerical results show that the supercapacitors based on coal-based carbon materials have great potential in high performance electrochemical energy storage.

N/S co-doped porous carbon spheres were prepared using one step strategy for high performance supercapacitors.     

Facile preparation of flexible binder-free graphene electrodes for high-performance supercapacitors

A facile two-step strategy to prepare flexible graphene electrodes has been developed for supercapacitors using thermal reduction of graphene oxide (GO) and thermally reduced graphene oxide (TRGO) composite films. The tunable porous structure of the GO/TRGO film provided channels to release the high pressure generated by CO₂ gas. The graphene electrode obtained from reduced-GO/TRGO (1 : 1 in mass ratio) film showed great flexibility and high film density (0.52 g cm⁻³). Using the EMI-BF₄ electrolyte with a working voltage of 3.7 V, the as-fabricated free-standing reduced-GO/TRGO (1 : 1) film achieved a great gravimetric capacitance of 180 F g⁻¹ (delivering a gravimetric energy density of 85.6 W h kg⁻¹), a volumetric capacitance of 94 F cm⁻³ (delivering a volumetric energy density of 44.7 W h L⁻¹), and a 92% retention after 10 000 charge/discharge cycles. In addition, the solid state flexible supercapacitor with the free-standing reduced-GO/TRGO (1 : 1) film as the electrodes and the EMI-BF₄/poly (vinylidene fluoride hexafluopropylene) (PVDF-HFP) gel as the electrolyte also demonstrated a high gravimetric capacitance of 146 F g⁻¹ with excellent mechanical flexibility, bending stability, and electrochemical stability. The strategy developed in this study provides great potentials for the synthesis of flexible graphene electrodes for supercapacitors.

A supercapacitor electrode is developed with a free-standing graphene film by a facile two-step strategy. The graphene electrode achieved a gravimetric capacitance of 180 F g⁻¹ and a volumetric capacitance of 94 F cm⁻³.     

Hierarchical porous carbons from carboxylated coal-tar pitch functional poly(acrylic acid) hydrogel networks for supercapacitor electrodes

A gel carbonization strategy for the synthesis of hierarchical porous carbons (HPCs) from carboxylated coal-tar pitches (CCP) functional poly(acrylic acid) (PAA) hydrogel networks for advanced supercapacitor electrodes was reported. The amphiphilic CCP and PAA polymer could be easily self-assembled to gel by the major driving force of hydrogen bonding and π–π stacking. The HPCs containing interconnected macro-/meso-/micropores were fabricated by direct carbonization of the dried hydrogels. The resultant HPCs with a high specific surface area and total pore volume of 1294.6 m² g⁻¹ and 1.34 cm³ g⁻¹ respectively, as a supercapacitor electrode exhibit a high specific capacitance of 292 F g⁻¹ at 1.0 A g⁻¹ in two-electrode system. The electrode also exhibits ultra-long cycle life with a capacitance retention as high as 94.2% after 10 000 cycles, indicating the good electrochemical stability. Furthermore, the concept of such hierarchical architecture and synthesis strategy would expand to other materials for advanced energy storage systems, such as Na-ion batteries and metal oxides for supercapacitors.

As a supercapacitor electrode exhibit a high specific capacitance of 292 F g⁻¹ at 1.0 A g⁻¹.     

An ultrasonic-assisted synthesis of rice-straw-based porous carbon with high performance symmetric supercapacitors

Biomass porous carbon materials are ideal supercapacitor electrode materials due to their low price, rich source of raw materials and environmental friendliness. In this study, an ultrasonic-assisted method was applied to synthesize the rice-straw-based porous carbon (UPC). The obtained UPC exhibited a two-dimensional structure and high specific surface area. In addition, the electrochemical test results showed that the UPC with a 1 hour ultrasonic treatment and lower activation temperature of 600 °C (UPC-600) demonstrated optimal performance: high specific capacitances of 420 F g⁻¹ at 1.0 A g⁻¹ and 314 F g⁻¹ at a high current of 10 A g⁻¹. Significantly, the symmetric supercapacitors showed a high energy density of 11.1 W h kg⁻¹ and power density of 500 W kg⁻¹. After 10 000 cycles, 99.8% of the specific capacitance was retained at 20 A g⁻¹. These results indicate that UPC-600 is a promising candidate for supercapacitor electrode materials.

Rice-straw-based porous carbon was successfully prepared via an ultrasonic-assisted method to lower activation temperature and for ultra-stable electrode materials of symmetric supercapacitors.     

Facile synthesis of bio-based nitrogen- and oxygen-doped porous carbon derived from cotton for supercapacitors

Biomass-derived O- and N-doped porous carbon has become the most competitive supercapacitor electrode material because of its renewability and sustainability. We herein presented a facile approach to prepare O/N-doped porous carbon with cotton as the starting material. Absorbent cotton immersed in diammonium hydrogen phosphate (DAP) was activated at 800 °C (CDAP800s) and then was oxidized in a temperature range of 300–400 °C. The electrochemical capacitance of the impregnated cotton was significantly improved by doping with O and N, and the yield was improved from 13% to 38%. The sample oxidation at 350 °C (CDAP800-350) demonstrated superior electrical properties. CDAP800-350 showed the highest BET surface area (1022 m² g⁻¹) and a relatively high pore volume (0.53 cm³ g⁻¹). In a three-electrode system, the CDAP800-350 electrodes had high specific capacitances of 292 F g⁻¹ in 6 M KOH electrolyte at a current density of 0.5 A g⁻¹. In the two-electrode system, CDAP800-350 electrode displayed a specific capacitance of 270 F g⁻¹ at 0.5 A g⁻¹ and 212 F g⁻¹ at 10 A in KOH electrolyte. In addition, the CDAP800-350-based symmetric supercapacitor achieved a high stability with 87% of capacitance retained after 5000 cycles at 5 A g⁻¹, as well as a high volumetric energy density (18 W h kg⁻¹ at 250 W kg⁻¹).

Biomass-derived O- and N-doped porous carbon has become one of the most competitive supercapacitor electrode material because of its renewability and sustainability.     

One-pot mechanochemical exfoliation of graphite and in situ polymerization of aniline for the production of graphene/polyaniline composites for high-performance supercapacitors

Graphene/polyaniline composites have attracted considerable attention as high-performance supercapacitor electrode materials; however, there are still numerous challenges for their practical applications, such as the complex preparation process, high cost, and disequilibrium between energy density and power density. Herein, we report an efficient method to produce graphene/polyaniline composites via a one-pot ball-milling process, in which aniline molecules act as both the intercalator for the exfoliation of graphite and the monomer for mechanochemical polymerization into polyaniline clusters on the in situ exfoliated graphene sheets. The graphene/polyaniline composite electrode delivered a large specific capacitance of 886 F g⁻¹ at 5 mV s⁻¹ with a high retention of 73.4% at 100 mV s⁻¹. The high capacitance and rate capability of the graphene/polyaniline composite can contribute to the fast electron/ion transfer and dominantly capacitive contribution because of the synergistic effects between the conductive graphene and pseudocapacitive polyaniline. In addition, a high energy density of 40.9 W h kg⁻¹ was achieved by the graphene/polyaniline-based symmetric supercapacitor at a power density of 0.25 kW kg⁻¹, and the supercapacitor also maintained 89.1% of the initial capacitance over 10 000 cycles.

Efficient ball-milling production of graphene/polyaniline composites as supercapacitor electrodes with enhanced capacitive contribution, rate capability, and specific capacitance.     

Ion accumulation-induced capacitance elevation in a microporous graphene-based supercapacitor

High-performance porous 3D graphene-based supercapacitors are one of the most promising and challenging directions for future energy technologies. Microporous graphene has been synthesized by the pyrolysis method. The fabricated lightweight graphene with a few layers (FLG) has an ultra-high surface area of 2266 m² g⁻¹ along with various-sized micropores. The defect-induced morphology and pore size distribution of the fabricated graphene are examined, and the results show that the micropores vary from 0.85 to 1.9 nm and the 1.02 nm pores contribute 30% of the total surface area. The electrochemical behaviour of the electrode fabricated using this graphene has been studied with various concentrations of the KOH electrolyte. The highest specific capacitance of the graphene electrode of 540 F g⁻¹ (close to the theoretical value, ∼550 F g⁻¹) can be achieved by using the 1 M KOH electrolyte. This high specific capacitance contribution involves the counter ion adsorption, co-ion desorption, and ion permutation mechanisms. The formation of a Helmholtz layer, as well as the diffusion of the electrolyte ions, confirms this phenomenon. The symmetrical solid-state supercapacitor fabricated with the graphene electrodes and PVA–KOH gel as the electrolyte exhibits excellent energy and power densities of 18 W h kg⁻¹ and 10.2 kW kg⁻¹, respectively. This supercapacitor also shows a superior 100% coulombic efficiency after 6000 cycles.

High-performance porous 3D graphene-based supercapacitors are one of the most promising and challenging directions for future energy technologies.     

“Water-in-salt” electrolyte enhanced high voltage aqueous supercapacitor with carbon electrodes derived from biomass waste-ground grain hulls

To design high specific surface area and optimize the pore size distribution of materials, we employ a combination of carbonization and KOH activation to prepare activated carbon derived from ground grain hulls. The resulting carbon material at lower temperature (800, BSAC-A-800) exhibits a porous structure with a high specific surface area of 1037.6 m² g⁻¹ and a pore volume of 0.57 m³ g⁻¹. Due to the synergistic structural characteristics, BSAC-A-800 reveals preferable capacitive performance, showing a specific capacitance as high as 313.3 F g⁻¹ at 0.5 A g⁻¹, good rate performance (above 73%), and particularly stable cycling performance (99.1% capacitance retention after 10 000 cycles at a current density of 10 A g⁻¹). More importantly, the assembled symmetric supercapacitor using a water-in-salt electrolyte (17 m NaClO₄) with high discharge specific capacitance (59 F g⁻¹ at 0.5 A g⁻¹), high energy density (47.2 W h kg⁻¹) and high voltage (2.4 V) represents significant progress towards performance comparable to that of commercial salt-in-water electrolyte supercapacitors (with discharge specific capacitance of 50 F g⁻¹, energy densities of ∼28.1 W h kg⁻¹ and voltages of 2.0 V).

To design high specific surface area and optimize the pore size distribution of materials, we employ a combination of carbonization and KOH activation to prepare activated carbon derived from ground grain hulls.     

Electrochemical performance of graphene-coated activated mesocarbon microbeads as a supercapacitor electrode

Hybrid activated carbon/graphene materials are prospective candidates for use as high performance supercapacitor electrode materials, since they have the superior characteristics of high surface area, abundant micro/mesoporous structure due to the presence of activated carbon and good electrical conductivity as a result of the presence of graphene. In this work, the electrochemical performance of facile and low-cost graphene-coated activated mesocarbon microbeads (g-AM) is carefully studied. The results show that g-AM can only be formed at a very high temperature over a long activation time, resulting in the formation of a large pore size and low specific surface area, further resulting in poor electrochemical performance (110 F g⁻¹ at 0.1 A g⁻¹ in 6 M KOH solution). Ball milling for a short time is an effective way to improve the electrochemical performance (191 F g⁻¹ at 0.1 A g⁻¹ in 6 M KOH solution). Moreover, due to the strong resistance to aggregation and good electrical conductivity of graphene flowers, the g-AM had nearly 100% rate capability when increasing the current density from 5 to 50 A g⁻¹. The as-assembled two-electrode symmetric supercapacitor exhibits a high energy and power density (5.28 W h kg⁻¹ at 10 000 W kg⁻¹) in organic LiPF₆ electrolyte, due to its better electrical conductivity. It is expected that this type of hybrid structure holds great potential for scalable industrial manufacture as supercapacitor electrodes.

Activated carbon/graphene materials are prospective candidates as high performance supercapacitor electrodes, due to the presence of aggregation resisted graphene on the surface of activated carbon.     

Template-assisted synthesis of NiCoO2 nanocages/reduced graphene oxide composites as high-performance electrodes for supercapacitors

Here we reported a coordinating etching and precipitating method to synthesize a complex binary metal oxides hollow cubic structure. A novel NiCoO₂/rGO composite with a structure of NiCoO₂ nanocages anchored on layers of reduced graphene oxide (rGO) were synthesized via a simple template-assisted method and the electrochemical performance was investigated by cyclic voltammetry, galvanostatic charge–discharge and electrochemical impedance spectroscopy tests as a faradaic electrode for supercapacitors at a graphene weight ratio of 1 wt% (1%). When used as electrode materials for electrochemical capacitors, the NiCoO₂/rGO composites achieved a specific capacity of 1375 F g⁻¹ at the current density of 1 A g⁻¹ and maintained 742 F g⁻¹ at 10 A g⁻¹. After 3000 cycles, the supercapacitor based on these nanocage structures shows long-term cycling performance with a high capacity of 778 F g⁻¹ at a current density of 1 A g⁻¹. These outstanding electrochemical performances are primarily attributed to the special morphological structure and the combination of mixed transition metal oxides and rGO, which not only maintains a high electrical conductivity for the overall electrode but also prevents the aggregation and volume expansion of electrochemical materials during the cycling processes.

Here we reported a coordinating etching and precipitating method to synthesize a complex binary metal oxides hollow cubic structure.     

Synthesis of 1,3-dicarbonyl-functionalized reduced graphene oxide/MnO2 composites and their electrochemical properties as supercapacitors

A novel 1,3-dicarbonyl-functionalized reduced graphene oxide (rDGO) was prepared by N-(4-aminophenyl)-3-oxobutanamide interacting with the epoxy and carboxyl groups of graphene oxide. The high-performance composite supercapacitor electrode material based on MnO₂ nanoparticles deposited onto the rDGO sheet (DGM) was fabricated by a hydrothermal method. The morphology and microstructure of the composites were characterized by field-emission scanning electron microscopy, transmission electron microscopy, Raman microscopy and X-ray photoelectron spectroscopy. The obtained results indicated that MnO₂ was successfully deposited on rDGO surfaces. The formed composite electrode materials exhibit excellent electrochemical properties. A specific capacitance of 267.4 F g⁻¹ was obtained at a current density of 0.5 A g⁻¹ in 1 mol L⁻¹ H₂SO₄, while maintaining high cycling stability with 97.7% of its initial capacitance after 1000 cycles at a current density of 3 A g⁻¹. These encouraging results are useful for potential energy storage device applications in high-performance supercapacitors.

A novel functionalized reduced graphene oxide and MnO₂ composite was prepared as a supercapacitor electrode material.     

Fe3O4 hard templating to assemble highly wrinkled graphene sheets into hierarchical porous film for compact capacitive energy storage

Highly wrinkled graphene film (HWGF) with high packing density was synthesized by combining an electrostatically self-assembling process, a vacuum filtration-induced film assembling process and capillary compression. Fe₃O₄ nanoparticles were used as a low-cost and environment-friendly hard template. Hierarchical porosity and high packing density were achieved with the aid of capillary compression in the presence of Fe₃O₄ nanoparticles. This strategy enables integration of highly wrinkled graphene sheets to form highly compact carbon electrodes with a continuous ion transport network. The generated HWGF exhibited a high packing density of 1.53 g cm⁻³, a high specific surface area of 383 m² g⁻¹ and a hierarchically porous structure. The HWGF delivered a high capacitance of 242 F g⁻¹ and 370 F cm⁻³ at 0.2 A g⁻¹ in 6 M KOH aqueous electrolyte system with excellent rate capability (202 F g⁻¹ and 309 F cm⁻³ retained at 20 A g⁻¹). The capacity retention rate reached 97% after 10 000 cycles at 1 A g⁻¹. The HWGF-based supercapacitor exhibited a high energy density of 17 W h kg⁻¹ at the power density of 49 W kg⁻¹. Such high capacitive performances could be attributed to the highly dense but porous graphene assemblies composed of highly wrinkled graphene sheets.

A facile strategy was reported to synthesize highly wrinkled graphene film, exhibiting high packing density and excellent capacitive performance.     

In situ hydrothermal synthesis of nickel cobalt sulfide nanoparticles embedded on nitrogen and sulfur dual doped graphene for a high performance supercapacitor electrode

Nickel cobalt sulfide nanoparticles (NCS) embedded onto a nitrogen and sulfur dual doped graphene (NS-G) surface are successfully synthesized via a two-step facile hydrothermal process. The electrical double-layer capacitor of NS-G acts as a supporting host for the growth of pseudocapacitance NCS nanoparticles, thus enhancing the synergistic electrochemical performance. The specific capacitance values of 1420.2 F g⁻¹ at 10 mV s⁻¹ and 630.6 F g⁻¹ at 1 A g⁻¹ are achieved with an impressive capability rate of 76.6% preservation at 10 A g⁻¹. Furthermore, the integrating NiCo₂S₄ nanoparticles embedding onto the NS-G surface also present a surprising improvement in the cycle performance, maintaining 110% retention after 10 000 cycles. Owing to the unique morphology an impressive energy density of 19.35 W h kg⁻¹ at a power density of 235.0 W kg⁻¹ suggests its potential application in high-performance supercapacitors.

Newly developed in situ hydrothermal synthesis governs morphology of Ni–Co–S embedded on N–S doped graphene thus providing exceptional capacitive behavior.     

Solvothermal synthesis of NiWO4 nanostructure and its application as a cathode material for asymmetric supercapacitors

This study proposes a facile solvothermal synthesis of nickel tungstate (NiWO₄) nanowires for application as a novel cathode material for supercapacitors. The structure, morphology, surface area and pore distribution were characterized and their capacitive performances were investigated. The results showed that the NiWO₄ nanowires synthesized in ethylene glycol solvent could offer a high specific capacitance of 1190 F g⁻¹ at a current density of 0.5 A g⁻¹ and a capacitance retaining ratio of 61.5% within 0.5–10 A g⁻¹. When used as a cathodic electrode of an asymmetric supercapacitor (ASC), the NiWO₄ nanowire based device can be cycled reversibly in a high-voltage region of 0–1.7 V with a high specific capacitance of 160 F g⁻¹ at 0.5 A g⁻¹, which therefore contributed to an energy density of 64.2 W h kg⁻¹ at a power density of 425 W kg⁻¹. Moreover, 92.8% of its initial specific capacitance can be maintained after 5000 consecutive cycles (5 A g⁻¹). These excellent capacitive properties make NiWO₄ a credible electrode material for high-performance supercapacitors.

This study proposes a facile solvothermal synthesis of nickel tungstate (NiWO₄) nanowires for application as a novel cathode material for supercapacitors.     

Pentafluoropyridine functionalized novel heteroatom-doped with hierarchical porous 3D cross-linked graphene for supercapacitor applications

The fabrication with high energy density and superior electrical/electrochemical properties of hierarchical porous 3D cross-linked graphene-based supercapacitors is one of the most urgent challenges for developing high-power energy supplies. We facilely synthesized a simple, eco-friendly, cost-effective heteroatoms (nitrogen, phosphorus, and fluorine) co-doped graphene oxide (NPFG) reduced by hydrothermal functionalization and freeze-drying approach with high specific surface areas and hierarchical pore structures. The effect of different heteroatoms doping on the energy storage performance of the synthesized reduced graphene oxide is investigated extensively. The electrochemical analysis performed in a three-electrode system via cyclic voltammetry (CV), galvanostatic charging–discharging (GCD), and electrochemical impedance spectroscopy (EIS) demonstrates that the nitrogen, phosphorous, and fluorine co-doped graphene (NPFG-0.3) synthesized with the optimum amount of pentafluoropyridine and phytic acid (PA) exhibits a notably enhanced specific capacitance (319 F g⁻¹ at 0.5 A g⁻¹), good rate capability, short relaxation time constant (τ = 28.4 ms), and higher diffusion coefficient of electrolytic cations (Dk⁺ = 8.8261 × 10⁻⁹ cm² s⁻¹) in 6 M KOH aqueous electrolyte. The density functional theory (DFT) calculation result indicates that the N, F, and P atomic replacement within the rGO model could increase the energy value (G_T) from −673.79 eV to −643.26 eV, demonstrating how the atomic level energy could improve the electrochemical reactivity with the electrolyte. The improved performance of NPFG-0.3 over NFG, PG, and pure rGO is mainly ascribed to the fast-kinetic process owing to the well-balanced electron/ion transport phenomenon. A symmetric coin cell supercapacitor device fabricated using NPFG-0.3 as the anode and cathode material with 6 M KOH aqueous electrolyte exhibits maximum specific energy of 38 W h kg⁻¹, a maximum specific power of 716 W kg⁻¹, and ∼88.2% capacitance retention after 10 000 cycles. The facile synthesis approach and promising electrochemical results suggest this synthesized NPFG-0.3 material has high potential for future supercapacitor application.

Demonstration of the effect of Gibbs free energy (G_T = −643.26 eV) on N, P, F co-doped graphene, simulated via density functional theory (DFT).     

Nitrogen and sulfur co-doped graphene aerogel for high performance supercapacitors

The development of high energy density and power density supercapacitors is very necessary in energy storage and application fields. A key factor of such devices is high-performance electrode materials. In this work, nitrogen and sulfur co-doped graphene aerogels (N/S-GA) were synthesized using graphene oxide as the precursor and 2-mercapto-1-methylimidazole as both the reducing agent and the N/S doping agent. The pore size distribution of the as-prepared N/S-GA was measured and the N/S-GA possesses a hierarchical porous structure. As an electrode material of supercapacitors, the N/S-GA could provide a suitable structure for charge accommodation and a short distance for ion transport. When 1-ethyl-3-methylimidazolium tetrafluoroborate ([Emim]BF₄) ionic liquid was used as the electrolyte, the specific capacitance of the N/S-GA electrode material reached 212 F g⁻¹ and 162 F g⁻¹ at the current densities of 1 A g⁻¹ and 10 A g⁻¹, respectively. And the energy density and average power density of the N/S-GA based supercapacitor could reach 117 W h kg⁻¹ and 1.0 kW kg⁻¹ at 1 A g⁻¹, 82 W h kg⁻¹ and 9.5 kW kg⁻¹ at 10 A g⁻¹, respectively. It is believed that the N/S-GA material can be used in high-performance supercapacitors.

A nitrogen and sulfur co-doped graphene aerogel (N/S-GA) was synthesised in one step, and N/S-GA based supercapacitors exhibited high performance.     

Nitrogen doped hierarchical activated carbons derived from polyacrylonitrile fibers for CO2 adsorption and supercapacitor electrodes

Nitrogen doped hierarchical activated carbons with high surface areas and different pore structures are prepared form polyacrylonitrile fibers through KOH activation by two steps. It is found that the specific surface area and porosity of the activated carbons depend strongly on the activation temperatures. The specific surface area increases from 607 m² g⁻¹ to 3797 m² g⁻¹ when the activation temperature increases from 600 °C to 800 °C, and then decreases to 3379 m² g⁻¹ at 900 °C. It shows that the hierarchical activated carbon prepared at a moderate activation temperature of 700 °C exhibits the largest CO₂ capture amount, i.e., 5.25 and 3.63 mmol g⁻¹ at 273 and 298 K, respectively, under the pressure of 1 bar. The excellent CO₂ capture properties are due to the high specific surface area of 2146 m² g⁻¹ and high nitrogen content (5.2 wt%) of the obtained sample. On the other hand, when used as supercapacitor electrodes, the sample with the activation temperature at 800 °C shows the largest specific capacitance of 302 F g⁻¹ at a current density of 1 A g⁻¹ in 6 M KOH aqueous electrolyte, with an excellent rate capability of 231 F g⁻¹ at 10 A g⁻¹. Furthermore, a nearly linear relationship between nitrogen content in the nitrogen doped activated carbons and specific CO₂ uptake as well as the specific capacitance were first established, indicating nitrogen doping was playing key roles in improving CO₂ adsorption and supercapacitor performance. The experimental results indicate that the thus obtained nitrogen doped hierarchical activated carbons are very promising for reducing CO₂ green house gas by adsorption as well as storing energy as utilized in supercapacitors.

Nitrogen doped activated carbons with high surface area up to 3797 m₂ g⁻¹ exhibit specific capacitance of 231 F g⁻¹ at a current density of 10 A g⁻¹.