Aqueous dispersions of carbon black and its hybrid with carbon nanofibers

The aqueous dispersions of a special type of carbon black (CB) in 1 M lithium bis(trifluoromethanesulfonimide) electrolyte is mainly controlled by the affinity of the aqueous electrolyte towards the CB particles rather than the particle size. In spite of its small particle size (30 nm), this type of CB forms a three-dimensional open network which is rheologically and electrically percolated at a relatively high threshold (2.0 wt%) with enhanced rheological and electrical properties. At this percolating threshold, replacing a trace amount of CB with equivalent carbon nanofibers (CNFs) produces hybrid dispersions with higher electrical conductivity and comparable rheological behavior to pure CB dispersions. This hybrid dispersion is dominated by a cooperatively supporting network, which is wired by the flexible filamentous nanofibers so that it is able to recover the conductivity loss under flow conditions due to flow-induced breaking up of the conductive pathways of CB and presumably sustain a higher load of active materials. This finding suggests hybrid dispersions as a promising precursor in the formulation of electrode suspensions for aqueous semi-solid redox flow cells.

Optimal hybrid dispersion of carbon black (CB) and nanofibers (CNFs) is formed at a critical content of CNFs before its aggregation concentration so that CNFs wire CB aggregates to recover the conductivity loss without increasing of CB rigidity.     

Pt-grown carbon nanofibers for detection of hydrogen peroxide

Removal of left-over catalyst particles from carbon nanomaterials is a significant scientific and technological problem. Here, we present the physical and electrochemical study of application-specific carbon nanofibers grown from Pt-catalyst layers. The use of Pt catalyst removes the requirement for any cleaning procedure as the remaining catalyst particles have a specific role in the end-application. Despite the relatively small amount of Pt in the samples (7.0 ± 0.2%), they show electrochemical features closely resembling those of polycrystalline Pt. In O₂-containing environment, the material shows two separate linear ranges for hydrogen peroxide reduction: 1–100 μM and 100–1000 μM with sensitivities of 0.432 μA μM⁻¹ cm⁻² and 0.257 μA μM⁻¹ cm⁻², respectively, with a 0.21 μM limit of detection. In deaerated solution, there is only one linear range with sensitivity 0.244 μA μM⁻¹ cm⁻² and 0.22 μM limit of detection. We suggest that the high sensitivity between 1 μM and 100 μM in solutions where O₂ is present is due to oxygen reduction reaction occurring on the CNFs producing a small additional cathodic contribution to the measured current. This has important implications when Pt-containing sensors are utilized to detect hydrogen peroxide reduction in biological, O₂-containing environment.

Application specific Pt-grown carbon nanofibers for H₂O₂ detection were characterized and the roles of dissolved oxygen and chloride ions on the electrochemical performance were assessed in detail.     

Flexible polypyrrolone-based microporous carbon nanofibers for high-performance supercapacitors

Flexible materials have drawn considerable attention due to the demand for wearable and flexible electronic products. Seeking new kinds of precursors for preparing carbon nanofibers with good flexibility for high-performance supercapacitors is a hot issue. In this work, a flexible polypyrrolone (BBB)/polyimide (PI) composite-based carbon nanofiber membrane (PBPICF) is prepared by a facile electrospinning and carbonization process. The PBPICF membranes exhibit a three-dimensional (3D) porous, fluffy and self-standing structure with good mechanical performance and flexibility, and can be arbitrarily bent and folded. PBPICF-65-35 (consisting of BBB (65 wt%) and PI (35 wt%)) exhibits a high specific capacitance of 172.44 F g⁻¹ in 6 M KOH aqueous solution, which is two-fold more than that of commercial polyacrylonitrile-based carbon nanofibers. In addition, PBPICF-65-35 also displays good power density (90 W kg⁻¹) and energy density (19.4 W h kg⁻¹), and the capacitance remains at 96% even after 10 000 cycles at 1.0 A g⁻¹. Therefore, the simple preparation and good capacitance performance of PBPICFs make them a promising binder-free electrode for wearable supercapacitors.

A flexible polypyrrolone (BBB)/polyimide (PI) composite-based carbon nanofiber membrane (PBPICF) has been prepared by a facile electrospinning and carbonization process.     

Facile synthesis of aqueous-dispersed luminescent nanosheets from non-layered lanthanum hexaboride

Two-dimensional nanosheets of non-layered materials have been considered as inaccessible through exfoliation techniques, due to their intrinsic three-dimensional lattice structure. Herein we report the successful synthesis of nanosheets from non-layered, lanthanum hexaboride through a facile, solution-assisted, surfactant-free, sonication. The morphological studies clearly show the presence of nanosheets having thickness of a few nanometers, and having lateral dimensions of several hundreds of nanometres. The as-fabricated nanosheets were found to be rich in hydroxyl groups, and hence exhibit excellent dispersion stability in water. The aqueous-dispersed nanosheets demonstrate excitation-wavelength dependent luminescence in the blue-cyan region, when excited with UV-light.

Nanosheets were synthesised by incorporating probe sonication and grinding of an aqueous dispersion of non-layered lanthanam hexaboride.     

Templated synthesis of microparticles with carbonaceous skeletal structures using polymer cubosomes as templates

Polymer cubosomes (PCs) are bicontinuous mesoporous colloidal particles that feature high surface areas and an extremely ordered crystalline pore network. PCs have attracted tremendous attention because of their potential applications in many fields. Herein, we obtained new microparticles with carbonaceous reticulated networks via templated synthesis using PCs as templates. The water-channel networks of the PCs were translated into a carbonaceous skeletal cubic structure. Carbon precursors were polymerized inside the water-channel networks of the PCs under acidic conditions without collapsing the internal crystalline mesophases. The carbonaceous interconnected networks created by the templated synthesis exhibited cubic crystalline skeletal networks similar to those of the PCs. These cubic-ordered mesoporous carbon (cOMC) microparticles exhibited several properties in electrochemical experiments. In addition, the nanoscopic structures and surfaces of these microparticles sustain electrochemically perturbing environments, and thus retain more than 90% capacitance after 1000 charge–discharge cycles.

Polymer cubosomes can be applied as templates for various mesoporous materials. By using polymer cubosomes, we have synthesized carbonaceous microparticles, which possess crystalline internal networks and exhibit electrochemical properties.     

Preparation and electrochemical studies of electrospun phosphorus doped porous carbon nanofibers

An ultra-facile fabrication process for the preparation of phosphorus doped porous carbon nanofibers (P-PCNFs) through the electrospinning and heat treatment method has been studied. The materials were characterized by X-ray diffraction, scanning electron microscopy, and X-ray photoelectron spectroscopy. Studies showed that fabricated P-PCNFs have unique porous fibers structures, large specific surface area (462.83 cm² g⁻¹), and abundant microporous and mesoporous structures. X-ray photoelectron spectroscopy analyses revealed that the contents of phosphorus and electrochemical properties in a series of P-PCNF samples can be tuned by controlling the polyphosphoric acid concentration. The electrochemical properties of the materials were evaluated using cyclic voltammetry, galvanostatic charge–discharge, and electrochemical impedance spectroscopy. Studies showed that the specific capacitance of the fabricated P-PCNFs using the ultra-facile process reached up to 228.7 F g⁻¹ at 0.5 A g⁻¹ in 1 M H₂SO₄. Over 84.37% of the initial capacitance remains as the current density increases from 0.5 to 10 A g⁻¹. Meanwhile, at a current density of 2 A g⁻¹, no capacitance loss was observed in 5000 charge/discharge cycles. The highest voltage windows of sample P-PCNFs-1.0 in 1 M H₂SO₄ aqueous electrolyte can reach 1.4 V. These properties suggest that the fabricated P-PCNFs exhibit excellent electrochemical properties. Conclusively, the surface of carbon nanofibers can be modified by heteroatom doping or surface activation which can improve the electrochemical performance of the materials.

Preparation of phosphorus-doped porous carbon nanofibers, with excellent capacitance properties, by electrospinning, using polyethylene glycol as a pore-making agent and polyphosphoric acid as a phosphorus source.     

N-Enriched carbon nanofibers for high energy density supercapacitors and Li-ion batteries

Nitrogen enriched carbon nanofibers have been obtained by one-step carbonization/activation of PAN-based nanofibers with various concentrations of melamine at 800 °C under a N₂ atmosphere. As synthesised carbon nanofibers were directly used as electrodes for symmetric supercapacitors. The obtained PAN-MEL fibers with 5% melamine stabilised at 280 °C and carbonized at 800 °C under a nitrogen atmosphere showed excellent electrochemical performance with a specific capacitance of up to 166 F g⁻¹ at a current density of 1A g⁻¹ using 6 M KOH electrolyte and a capacity retention of 109.7% after 3000 cycles. It shows a 48% increase as compared to pristine carbon nanofibers. Two electrode systems of the CNFM5 sample showed high energy densities of 23.72 to 12.50 W h kg⁻¹ at power densities from 400 to 30 000 W kg⁻¹. When used as an anode for Li-ion battery application the CNFM5 sample showed a high specific capacity up to 435.47 mA h g⁻¹ at 20 mA g⁻¹, good rate capacity and excellent cycling performance (365 mA h g⁻¹ specific capacity even after 200 cycles at 100 mA g⁻¹). The specific capacity obtained for these nitrogen enriched carbon nanofibers is higher than that for pristine carbon nano-fibers.

Nitrogen enriched carbon nanofibers have been obtained by one-step carbonization/activation of PAN-based nanofibers with various concentrations of melamine at 800 °C under a N₂ atmosphere.     

Co9S8 nanoparticle-decorated carbon nanofibers as high-performance supercapacitor electrodes

This work reported Co₉S₈ nanoparticle-decorated carbon nanofibers (CNF) as a supercapacitor electrode. By using a mild ion-exchange method, the cobalt oxide-based precursor nanoparticles were transformed to Co₉S₈ nanoparticles in a microwave hydrothermal process, and these nanoparticles were decorated onto a carbon nanofiber backbone. The composition of the nanofibers can be readily tuned by varying the Co acetate content in the precursor. The porous carbon nanofibers offered a fast electron transfer pathway while the well dispersed Co₉S₈ nanoparticles acted as the redox center for energy storage. As a result, high specific capacitance of 718 F g⁻¹ at 1 A g⁻¹ can be achieved with optimized Co₉S₈ loading. The assembled asymmetric supercapacitor with Co₉S₈/CNF as the cathode showed a high energy density of 23.8 W h kg⁻¹ at a power density of 0.75 kW kg⁻¹ and good cycling stability (16.9% loss over 10 000 cycles).

Through electrospinning and the ion-exchange method, Co₉S₈ nanoparticle-decorated carbon nanofibers (Co₉S₈/CNF) have been fabricated, and exhibit good supercapacitor performance.     

Pt-grown carbon nanofibers for enzymatic glutamate biosensors and assessment of their biocompatibility

Application-specific carbon nanofibers grown from Pt-catalyst layers have been shown to be a promising material for biosensor development. Here we demonstrate immobilization of glutamate oxidase on them and their use for amperometric detection of glutamate at two different potentials. At −0.15 V vs. Ag/AgCl at concentrations higher than 100 μM the oxygen reduction reaction severely interferes with the enzymatic production of H₂O₂ and consequently affects the detection of glutamate. On the other hand, at 0.6 V vs. Ag/AgCl enzyme saturation starts to affect the measurement above a glutamate concentration of 100 μM. Moreover, we suggest here that glutamate itself might foul Pt surfaces to some degree, which should be taken into account when designing Pt-based sensors operating at high anodic potentials. Finally, the Pt-grown and Ni-grown carbon nanofibers were shown to be biocompatible. However, the cells on Pt-grown carbon nanofibers had different morphology and formation of filopodia compared to those on Ni-grown carbon nanofibers. The effect was expected to be caused rather by the different fiber dimensions between the samples than the catalyst metal itself. Further experiments are required to find the optimal dimensions of CNFs for biological purposes.

Pt-grown carbon nanofibers were utilized for the fabrication of glutamate biosensors and in addition their biocompatibility was assessed.     

The preparation of liquefied bio-stalk carbon nanofibers and their application in supercapacitors

Carbon nanofibers (CNFs) have been widely used in electrochemical energy storage devices because of their excellent conductivity, extremely large surface area and structural stability. Herein, we obtained a viscous, liquefied bio-stalk carbon via the simple chemical treatment of biomass, and mixed it with polyacrylonitrile to prepare a spinning solution. Subsequent electrospinning and high temperature activation resulted in the successful preparation of liquefied lignin-based activated carbon nanofibers. The as-prepared liquefied bio-stalk carbon nanofibers exhibited an outstanding electrochemical performance (specific capacitance of 273 F g⁻¹ at 0.5 A g⁻¹ current density), and a capacitance retention of 210 F g⁻¹ even under a large current density of 10 A g⁻¹. Besides its high specific capacitance and outstanding rate capability, the symmetrical supercapacitor cell based on the liquefied carbon-based nanofiber electrodes also exhibited an excellent cycling performance with 92.76% capacitance retention after 5000 charge–discharge cycles. This study provides a new strategy for the future development of supercapacitor electrode materials and enhances the development of biomass energy.

Carbon nanofibers (CNFs) have been widely used in electrochemical energy storage devices because of their excellent conductivity, extremely large surface area and structural stability.     

Li–fluorine codoped electrospun carbon nanofibers for enhanced hydrogen storage

Carbon materials have attracted increasing attention for hydrogen storage due to their great specific surface areas, low weights, and excellent mechanical properties. However, the performance of carbon materials for hydrogen absorption is hindered by weak physisorption. To improve the hydrogen absorption performance of carbon materials, nanoporous structures, doped heteroatoms, and decorated metal nanoparticles, among other strategies, are adopted to increase the specific surface area, number of hydrogen storage sites, and metal catalytic activity. Herein, Li–fluorine codoped porous carbon nanofibers (Li–F–PCNFs) were synthesized to enhance hydrogen storage performance. Especially, perfluorinated sulfonic acid (PFSA) polymers not only served as a fluorine precursor, but also inhibited the agglomeration of lithium nanoparticles during the carbonization process. Li–F–PCNFs showed an excellent hydrogen storage capacity, up to 2.4 wt% at 0 °C and 10 MPa, which is almost 24 times higher than that of the pure porous carbon nanofibers. It is noted that the high electronegativity gap between fluorine and lithium facilitates the electrons of the hydrogen molecules being attracted to the PCNFs, which enhanced the hydrogen adsorption capacity. In addition, Li–F–PCNFs may have huge potential for application in fuel cells.

We developed a facile, yet general, approach for preparing Li–fluorine codoped porous carbon nanofiber (Li–F–PCNF) composites, which showed excellent hydrogen storage performance.     

Growth of narrow-bandgap Cl-doped carbon nitride nanofibers on carbon nitride nanosheets for high-efficiency photocatalytic H2O2 generation

Heterojunction construction has been proved to be an effective way to enhance photocatalysis performance. In this work, Cl-doped carbon nitride nanofibers (Cl–CNF) with broadband light harvesting capacity were in situ grown on carbon nitride nanosheets (CNS) by a facile hydrothermal method to construct a type II heterojunction. Benefiting from the joint effect of the improved charge carriers separation efficiency and a broadened visible light absorption range, the optimal heterostructure of Cl–CNF/CNS exhibits a H₂O₂ evolution rate of 247.5 μmol g⁻¹ h⁻¹ under visible light irradiation, which is 3.4 and 3.1 times as much as those of Cl–CNF (72.2 μmol g⁻¹ h⁻¹) and CNS (80.2 μmol g⁻¹ h⁻¹), respectively. Particularly, the heterojunction nanostructure displays an apparent quantum efficiency of 23.67% at 420 nm. Photoluminescence spectra and photocurrent measurements both verified the enhanced charge carriers separation ability. Our work provides a green and environmentally friendly strategy for H₂O₂ production by elaborate nanostructure design.

The Cl-CNF/CNS heterostructure can efficiently boost the photocatalytic H₂O₂ generation activity.     

Enhanced microwave absorption performance of light weight N-doped carbon nanoparticles

Microwave absorbents with specific morphology and structure have fundamental significance for tuning microwave absorption (MA). Herein, N-doped carbon sphere nanoparticles and hollow capsules were successfully fabricated via oxidative polymerization of dopamine in different mixed solutions, without any template preparation or etching process. Compared to solid particles, the microwave absorbents consisting of N-doped carbon with a hollow structure showed enormously enhanced MA performance, exhibiting a broad effective absorption bandwidth (from 12.7 GHz to 17.9 GHz) and a minimum reflection loss of −27.2 dB with a sample thickness of 2.0 mm. This work paves an attractive way for simple and eco-friendly preparation of advanced light weight microwave absorbents.

N-doped carbon particles were prepared through environmentally friendly and convenient methods. N-doped carbon capsules exhibit the best microwave absorption ability compared to their spherical counterparts.     

Recent progress of MOF-derived porous carbon materials for microwave absorption

Microwave absorbing materials (MAM) have attracted considerable attention over the years in stealth and information technologies. Metal–organic framework (MOF) with a unique microstructure and electronic state has become an attractive focus as self-sacrificing precursors of microwave absorbers. The MOF-derived porous carbon (PC) materials exhibit a high absorbing performance due to the stable three-dimensional structure and homogeneous distribution of metal particles. MOF-derived PC materials are promising for ideal MAM via tuning of the structure and composition, resulting in appropriate impedance matching and the synergistic effect between magnetic and dielectric loss. In this review, the MOF-derived PC materials and their basic absorption mechanisms (dielectric loss, magnetic loss and impedance matching) are introduced, as well as the characters of various MOF-derived PC materials. In addition, this review provides a comprehensive introduction and tabulates the recent progress based on the classification of the MOF-derived metallic state, such as pure PC (without reduced metals), mono-metal/PC, multi-metal/PC, metal oxides/PC and other derived PC composites. Finally, the challenges faced by MOF-derived PC materials are overviewed, and their further development is mentioned.

MOF-derived PC materials with unique characteristic have been widely concerned as microwave absorbers over the years.     

The carbonization of polyacrylonitrile-derived electrospun carbon nanofibers studied by in situ transmission electron microscopy

Cathode structures derived from carbonized electrospun polyacrylonitrile (PAN) nanofibers are a current line of development for improvement of gas diffusion electrodes for metal–air batteries and fuel cells. Diameter, surface morphology, carbon structure and chemical composition of the carbon based fibers play a crucial role for the functionality of the resulting cathodes, especially with respect to oxygen adsorption properties, electrolyte wetting and electronic conductivity. These functionalities of the carbon fibers are strongly influenced by the carbonization process. Hitherto, fibers were mostly characterized by ex situ methods, which require great effort for statistical analysis in the case of microscopy. Here, we show the morphological and structural evolution of nanofibers during their carbonization at up to 1000 °C by in situ transmission electron microscopy (TEM). Changes in fiber diameter and surface morphology of individual nanofibers were observed at 250 °C, 600 °C, 800 °C and 1000 °C in imaging mode. The structural evolution was studied by concomitant high resolution TEM and electron diffraction. The results show with comparatively little effort shrinkage of the nanofiber diameter, roughening of the surface morphology and formation of turbostratic carbon with increasing carbonization temperature at identical locations.

The carbonization of polyacrylonitrile (PAN) nanofibers is observed in situ up to 1000 °C by transmission electron microscopy (TEM).     

Role of alkan-1-ol solvents in the synthesis of yellow luminescent carbon quantum dots (CQDs): van der Waals force-caused aggregation and agglomeration

Carbon quantum dots (CQDs; luminescent carbon nanoparticles, size < 10 nm) have attracted much attention with respect to their eco-friendliness and multi-functionality. The solvent-dependent photoluminescence of CQDs has been well investigated to optimize the synthesis process and homogeneous dispersion. Although some alkan-1-ol solvents, such as ethanol, have been well utilized empirically as good solvents when synthesizing highly photoluminescent CQDs, the role of alkan-1-ol solvents, particularly long-chain alkan-1-ols (e.g., 1-nonanol, 1-decanol), has not yet been clarified. Herein, we demonstrate a method for the synthesis of strongly yellow emitting CQDs using solvothermal treatment and elucidate the role of alkan-1-ol solvents in the photoluminescence of CQDs. These CQDs have been characterized using theoretical calculations, ex situ morphological observations using transmission electron microscopy (TEM) and dynamic light scattering (DLS), and 500 MHz ¹H nuclear magnetic resonance (NMR) and ¹³C NMR spectroscopy. A comparative study of alkan-1-ol solvents suggests a mechanism for the agglomeration and aggregation of carbon precursors, intermediates, and CQDs, which is expected to lead to further synthesis studies on highly luminescent CQDs.

Carbon quantum dots (CQDs; luminescent carbon nanoparticles, size < 10 nm) have attracted much attention with respect to their eco-friendliness and multi-functionality.     

A flexible and highly sensitive pressure sensor based on three-dimensional electrospun carbon nanofibers

High-performance flexible pressure sensors with high sensitivity are important components of the systems for healthcare monitoring, human–machine interaction, and electronic skin. Herein, a flexible and highly sensitive pressure sensor composed of ferrosoferric oxide (Fe₃O₄)/carbon nanofibers (FeOCN) was fabricated using three-dimensional electrospinning and further heat treatment methods. The obtained pressure sensor demonstrates a wide working range (0–4.9 kPa) and a high sensitivity of 0.545 kPa⁻¹ as well as an ultralow detection limit of 6 Pa. Additionally, the pressure sensor exhibits a rapid response time, good stability, high hydrophobicity, and excellent flexibility. These merits endow the pressure sensor with the ability to precisely detect wrist pulse, phonation, breathing, and finger bending in real-time. Therefore, the FeOCN pressure sensor presents a promising application in real-time healthcare monitoring.

A three-dimensional electrospun carbon nanofiber network was used to measure press strains with high sensitivity.     

Simultaneous ultraviolet and first near-infrared window absorption of luminescent carbon dots/PVA composite film

Liquid Carbon Dots (CDs) were successfully synthesized by hydrothermal method using urea and citric acid as raw materials. TEM images confirmed that the CDs have a spherical shape with a homogeneous distribution. The as-prepared liquid CDs could absorb ultraviolet (UV) and first near infra-red (NIR) window simultaneously. However, the photoluminescence (PL) of the liquid CDs was damaged by their quenching effect. To overcome this issue, the liquid CDs were dispersed in poly(vinyl) alcohol (PVA) to fabricate the composite film. Herein, the dual-peak absorption properties of the CDs/PVA composite films were investigated for the first time. The composite films could maintain the simultaneous UV and first NIR window absorption property even after being preheated up to 200 °C, implying that the structure of CDs was well retained during the transition from the liquid to films. Daylight treatment for seven days produced minimum changes in the UV-vis and PL spectra, which indicates that the CDs/PVA film has more stable optical properties than the liquid CDs.

The simultaneous UV and first NIR absorption of the CDs/PVA composite could be maintained up to 200 °C, with minimum PL changes.     

Simplifying the synthesis of carbon inverse opals

Carbon inverse opals (IOs) were prepared via a facile synthesis approach using a sucrose-based precursor and polystyrene (PS) spheres as a sacrificial template. During IO preparation, polymer spheres are typically removed by dispersion in organic solvents, such as toluene or tetrahydrofuran. In this study, carbon IOs are prepared with and without removal of PS spheres by toluene to determine the influence of template removal prior to high-temperature treatment on the morphology and chemistry of the resulting carbons. Properties of samples are compared through a systematic investigation by electron microscopy, Fourier-transform infrared spectroscopy and Raman spectroscopy. We demonstrate that a commonly used processing step—polymer sphere template chemical removal—does not make any significant difference to the IO morphology. A correlation of Raman spectroscopy with SEM imaging and TGA analysis indicates that carbon IOs prepared without the solvent-treatment step are more ordered than samples prepared with this processing step. The key finding of this report is the simplified IO synthesis procedure, which can be adapted to the preparation of IOs of other materials besides carbon.

A simplified synthesis method to prepare carbon inverse opals is presented, which is applicable to other inverse opal materials.     

Bacterial cellulose-derived carbon nanofibers as both anode and cathode for hybrid sodium ion capacitor

Hybrid ion capacitors (HICs) based on insertion reactions have attracted considerable attention due to their energy density being much higher than that of the electrical double-layer capacitors (EDLCs). However, the development of hybrid ion capacitors with high energy density at high power density is a big challenge due to the mismatch of charge storage capacities and electrode kinetics between the battery-type anode and capacitor-type cathode. In this work, N and O dual doped carbon nanofibers (N,O-CNFs) were combined with carbon nanotubes (CNTs) to compose a complex carbon anode. N,O dual doping effectively tuned the functional group and surface activity of the CNFs while the integration of CNTs increased the extent of graphitization and electrical conductivity. The carbon cathode with high specific surface area and high capacity was obtained by the activation of CNFs (A-CNFs). Finally, a hybrid sodium ion capacitor was constructed by the double carbon electrode, which showed a superior electrochemical capacitive performance. The as-assembled HIC device delivers a maximum energy density of 59.2 W h kg⁻¹ at a power density of 275 W kg⁻¹, with a high energy density of 38.7 W h kg⁻¹ at a power density of 5500 W kg⁻¹.

A hybrid sodium ion capacitor is constructed by the double carbon electrode, whose precursors are both from nanofibers of bacterial cellulose, showing a superior electrochemical capacitive performance.