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In this study, an electrospinning method was used to produce highly conductive freestanding carbon nanofibers (CNFs). The freestanding CNFs are compatible with hierarchical growth techniques, such as hydrothermal processes, for the nanostructure engineering of supercapacitor electrodes with enhanced electrochemically active sites. Therefore, the flower-like FeMoO 4 @CNF nanosheets were investigated to improve the electrochemical performance using aqueous and neutral electrolytes (Na 2 SO 4 and K 2 SO 4). The optimized FeMoO 4 @CNF electrode exhibits areal capacitances of 252 and 220 mF·cm−2 at a high current density of 2.5 mA·cm−2 with Na 2 SO 4 and K 2 SO 4 electrolytes, respectively. The wide potential window (1.6 V) of the symmetric supercapacitor delivered maximum energy densities of 22.4 and 19.6 μWh·cm−2 at a power density of 2 mW·cm−2 for Na 2 SO 4 and K 2 SO 4 electrolytes, respectively. [ABSTRACT FROM AUTHOR]

Sub-fluorinated carbon nanofibers (F-CNFs) can be described as a non-fluorinated core surrounded by a fluorocarbon lattice. The core ensures the electron flux in the cathode during the electrochemical discharge in the primary lithium battery, which allows a high-power density to be reached. The ball-milling in an inert gas (Ar) of these F-CNFs adds a second level of conductive sp2 carbons, i.e., a dual sub-fluorination. The opening of the structure changes, from one initially similar multi-walled carbon nanotube to small lamellar nanoparticles after milling. The power densities are improved by the dual sub-fluorination, with values of 9693 W/kg (3192 W/kg for the starting material). Moreover, the over-potential of low depth of discharge, which is typical of covalent CFx, is suppressed thanks to the ball-milling. The energy density is still high during the ball-milling, i.e., 2011 and 2006 Wh/kg for raw and milled F-CNF, respectively. [ABSTRACT FROM AUTHOR]

[Display omitted] • 1D skin-core multilayer structure was fabricated by a facile template method. • Bicontinuous electron/ion transport during the charge/discharge process. • The large specific surface area and hollow hierarchical porous structure. • Adjusting active layers or sites can obviously improve the capacitive properties. • The maximum energy density of 8.77 Wh kg−1 at a power density of 0.25 kW kg−1. The fast transport of electrons and ions within electrodes is crucial to the final electrochemical properties. Herein, we have developed a unique ultra-long one-dimensional (1D) skin-core multilayer structure based on electrospun carbon nanofibers mainly through a facile Stöber method combined with resorcinol–formaldehyde resin, which not only achieves bicontinuous electron/ion transport during the charge/discharge process, but also provides large surface area for ion adsorption. Particularly, controlling the number of active layers as well as regulating the active sites in layer both can obviously improve capacitive properties. Benefiting from the synergistic effects of the desirable architecture, such the rational-designed skin-core structural carbon nanofibers as supercapacitor electrode can deliver a high specific capacitance up to 255 F g−1 at 0.5 A g−1, favorable rate capability with 89% capacitance retention of initial capacitance at 8 A g−1, and excellent cycling stability with nearly 93% capacity retention after 10,000 cycles at 2 A g−1. Furthermore, the as-assembled symmetric supercapacitor devices also present a maximum energy density of 8.77 Wh kg−1 at 0.25 kW kg−1 and a maximum power density of 3.70 kW kg−1 at 6.74 Wh kg−1. Such skin-core carbon nanofibers provide an effective strategy to design high-performance supercapacitor electrode for the next-generation energy storage devices. [ABSTRACT FROM AUTHOR]

Herein, MnO2 nanoflowers are electrodeposited on a self-supported and electroconductive electrode in which 2D Ti3C2Tx nanosheets are encased in carbon nanofibers (MnO2@Ti3C2Tx/CNFs). This improves the conductivity and hydrophilicity of the MnO2 composite electrode. The asymmetric supercapacitor shows a high energy density of 46.4 W h kg−1 and a power density of 4 kW kg−1. [ABSTRACT FROM AUTHOR]

Triple-layered boron-containing carbon nanofibers (CNFs) with hollow channels (PPMPB) are fabricated via step-by-step electrospinning for high-performance freestanding supercapacitors. Polyacrylonitrile (PAN)-based CNFs in the first layer are chosen as the support layer material because of their excellent chemical stability and electrospinnability. The well-developed hollow channels provided fast ion diffusion in the second layer of PAN/poly(methyl methacrylate) (PMMA)-based CNFs. The surface boron functional groups constituting the third layer contribute to the pseudo-capacitance. The symmetric supercapacitor of the PPMPB electrodes delivers a maximum specific capacitance of 180 Fg−1 at 1 mAcm−2, a high energy density of 22.38 Whkg−1 at a power density of 400 Wkg−1, and an excellent retention rate of 96% after 10,000 cycles in aqueous solution. The excellent electrochemical performance is attributed to the unique sandwich nanostructure with a three-layer structure, in which the factors representing the electrochemical properties of each layer do not interfere with each other. Therefore, a moderate amount of boron and the high surface area of the triple-layer structured PPMPB can be fully utilized as an excellent conductive network and electroactive sites, which is expected in a high-performance supercapacitor electrode. [Display omitted] • Triple-layered boron-containing CNFs were fabricated by step-by-step electrospinning. • The CNFs in the first layer provide active adsorption sites for EDLC. • Hollow core present in the interlayer serves as an excellent conductive network. • A moderate amount of boron in the third layer is utilized as the electroactive site. • Symmetric PPMPB(20) electrode showed good rate capability and long cycle life. [ABSTRACT FROM AUTHOR]

Highly graphitic porous carbon was derived from kelp biomass and prepared using KOH as the main activating agent with K2FeO4 as the assisting activated agent for supercapacitor applications. The optimum K2FeO4 mass in the total activating agent and temperature were investigated. The characterization results showed porous sheet carbon with a high specific surface area of 2868 m2 g−1 and a low ID/IG of 0.909. It delivered an excellent specific capacitance of 438 F g−1 at 0.5 A g−1. In addition, the assembled supercapacitor device reached the highest energy density of 19.9 W h kg−1 with a power density of 398 W kg−1. [ABSTRACT FROM AUTHOR]

[Display omitted] • • Developed pure Si anode for enhanced LIC power density and energy density. • • Functional layers with hydrophilic groups enhance electrode adhesion. • • Functional cover suppresses volume expansion of electrode. • • Functional cover forms stable inorganic-rich SEI reducing electrode degradation. • • Achieved high energy and power density with stable cycle stability in full-cell. A lithium–ion capacitor, comprising a capacitor–type cathode and battery–type anode, exhibits high power and energy density; however, the integration of different charge storage mechanisms in one cell naturally leads to a kinetic mismatch between the two electrodes, reducing the power density and cycle stability. To solve this problem, high–capacity anode materials with thinner electrodes are required. Silicon, with its high specific capacity, is considered a promising anode material with high energy and power density; however, pure Si anodes undergo rapid capacity fading and exhibit increased internal resistance owing to volume changes during cycling. In this study, both sides of the electrode are covered with functional layers consisting of functionalized herringbone–type carbon nanofibers to protect the Si electrode from degradation. The polar functional groups on the nanofibers weakly interact with the native oxide layer of the Si surface and the carboxyl groups of the binder, ensuring stable contact between electrode materials over repeated cycles. Moreover, the conductive functional cover promotes uniform lithium ion fluxes, aiding the formation of a stable solid electrolyte interphase layer. This study investigates the effects of this strategy on pure Si electrodes by surface morphology analysis, assessment of chemical interactions, and electrochemical testing. This approach has the potential to overcome the degradation of Si electrodes and significantly improve the power and energy density of lithium–ion capacitors. [ABSTRACT FROM AUTHOR]

The synthesis of Laser-Induced Graphene (LIG) through the laser ablation process of carbon-containing materials is a rapid and scalable process which enables the production of graphene in a cost-effective manner. In recent years, metal oxide – graphene composite electrodes have gained a lot of importance due to their use in various Energy Storage Devices (ESDs). In our investigation, we manufacture composite electrodes of manganese dioxide (MnO 2) and LIG through a hydrothermal process and use it as electrodes in Flexible Supercapacitors. This method deviates from traditional procedures as it eliminates the requirement for binders in creating composite electrodes, given that MnO 2 can be directly deposited onto the LIG electrodes. The assembled all-Flexible Supercapacitor (FSC), featuring unique LIG-MnO 2 composite electrodes, showcased a remarkable areal capacitance of 66.5 mF cm−2 at 5 mV s−1 scan rate. The device also exhibited a very high areal energy density (2.3 mWh cm−2) and power density (19.7 mW cm−2) at 0.2 mA cm−2 current density. Also, 82 % capacitance retention was observed at the end of 2000 cycles and the device also exhibited a good flexibility during bending tests, as evidenced by an 80 % capacitance retention after 100 bending cycles. [ABSTRACT FROM AUTHOR]

Sodium‐ion hybrid capacitors (SIHCs) have been regarded as one of the promising energy devices thanks to its low cost and compromise between energy density and power density, yet remain a challenge towards practical levels of mass loading (>10 mg cm−2). Herein, the fabrication of a 1D core–shell structure is reported with N‐doped porous carbon encapsulating ZnV2O4 nanofibers (ZnV2O4NFs@N‐PC), which features an open framework and favorable properties for facilitating ion diffusion, mass transportation, and electron transfer, enabling it to perform impressively for sodium ions storage. A 3D printed SIHC is conceptually proposed by coupling the 3D printed ZnV2O4NFs@N‐PC anode with a 3D printed active carbon cathode, which can deliver a high energy/power density of 145.07 Wh kg−1/3677.1 W kg−1 with a durable cycling lifespan. It is demonstrated that the 3D printed SIHC, even at a high mass loading of up to 16.25 mg cm−2, can release a high areal energy/power density of 1.67 mWh cm−2/38.96 mW cm−2, outperforming most of the SIHCs developed so far. The present work sheds light on the role of the design of electrode materials and verifies the promise of 3D‐printed technology for next‐generation electrochemical energy devices. [ABSTRACT FROM AUTHOR]

N/P dual-doped three-dimensional porous carbon was synthesized via nano-CaCO 3 template-assistant carbonization of intumescent flame retardants (IFRs) precursor. [Display omitted] Heteroatom-doped three-dimensional (3D) porous carbons possess great potential as promising electrodes for high-performance supercapacitors. Inspired by the inherent features of intumescent flame retardants (IFRs) with universal availability, rich heteroatoms and easy thermal-carbonization to form porous carbons, herein we proposed a self-assembling and template self-activation strategy to produce N/P dual-doped 3D porous carbons by nano-CaCO 3 template-assistant carbonization of IFRs. The IFRs-derived carbon exhibited large specific surface area, well-balanced hierarchical porosity, high N/P contents and interconnected 3D skeleton. Benefitting from these predominant characteristics on structure and composition, the assembled supercapacitive electrodes exhibited outstanding electrochemical performances. In three-electrode 6 M KOH system, it delivered high specific capacitances of 407 F g−1 at 0.5 A g−1, and good rate capability of 61.2% capacitance retention at 20 A g−1. In two-electrode organic EMIMBF 4 /PC system, its displayed high energy density of 62.8 Wh kg−1 at a power density of 748.4 W kg−1, meanwhile it had excellent cycling stability with 84.7% capacitance retention after 10,000 cycles. To our best knowledge, it is the first example to synthesize porous carbon from IFRs precursor. Thus, the current work paved a novel and low-cost way for the production of high-valued carbon material, and expanded its application for high-performance energy storage devices. [ABSTRACT FROM AUTHOR]

It is difficult for green sustainable lignin-based materials to simultaneously obtain efficient electromagnetic wave absorption (EMWA) and supercapacitive energy storage (SCES), which has not yet been reported. Herein, the light-weight lignin-based carbon nanofibers (LCNFs) with proper pore size, well graphitization degree, and heteroatom doping were tailored through electrospinning and carbonization processes. Interestingly, the graphitization degree and porous structure of LCNFs could be easily adjusted by changing the activating temperature, and the higher conductivity was achieved for preparing LCNFs at higher activating temperature due to the differences in the crystal size and activating degree of LCNFs. As a result, in the field of EMWA, the LCNFs-950 exhibited the minimum reflection loss (RL) value was −41.4 dB and the absorbing frequency was 9.05 GHz at 2.5 mm thickness, which meant this absorbent could absorb and/or dissipate more than 99.9% of incident electromagnetic wave (EMW). Furthermore, the LCNFs-950 also exhibited excellent SCES ability. In two-electrode system, the optimal LCNFs-950 symmetric supercapacitor specific capacitance reached 139.4 F/g at a current density of 0.5 A/g, meanwhile, the energy density was 41.4 Wh/kg at a power density of 3500 W/Kg. These multifunctional features of LCNFs will be highly promising for the next-generation environmental remediating materials. [Display omitted] • Increasing the activating temperature was an effective strategy for preparing renewable and low-cost multifunction LCNFs. • Multifunction LCNFs in both electromagnetic wave absorption and electrochemical energy storage were fabricated. • The minimum reflection loss was −41.4 dB and the absorbing frequency was 9.05 GHz at 2.5 mm thickness. • The specific capacitance, energy density and power density were up to 139.4 F/g, 41.4 Wh/kg and 3500 W/Kg, respectively. [ABSTRACT FROM AUTHOR]

Thin carbon nanofibers (TCNFs) hanging on branched carbon nanofibers (3D TCNF/CNF) with an N-doping level up to 8.7 at% for high-performance supercapacitors are designed and synthesized. TCNF/CNF shows a 3D hierarchical porous structure, a large surface area, abundant ionic-channels, and a great number of electrochemically active sites by N-doping. Because of the multiple synergistic effects of these features, the supercapacitors (SCs) based on TCNF/CNF show a remarkably excellent electrochemical behavior with a high specific capacitance of 224 F g−1. After 50 000 cycles of charge/discharge, 92% of the initial capacitance value is retained in 1.0 M H2SO4 electrolyte. Moreover, the TCNF/CNF-based SCs show low internal resistance, leading to a high power density with a relatively high energy density. [ABSTRACT FROM AUTHOR]

Prussian blue analogs, as a pseudo-capacitor electrode materials hold great potential due to their unique framework structure, excellent electrochemical activity and high specific capacity. Herein, a versatile method for the growth of series of metal hexacyanoferrates (MHCF) on carbon nanofiber with high conductivity and flexibility was proposed. By controlling the releasing rate of metal ions through acid modulation of solution, the series of MHCF nanocubes were successfully embedded on the carbon nanofibers with super stability. Different MHCF presented various loading density. Among the MHCFs, nickel hexacyanoferrate (NiHCF) is the most easily formed with high density and uniform distribution. The obtained self-supporting NiHCF@CNF, as a representative electrode, exhibited high specific capacitance (507 F g−1, 1 A g−1) and remarkable rate performance (67% retention at 10 A g−1). Moreover, the NiHCF@CNF-based hybrid supercapacitor cell delivered a high energy density of 60 Wh kg−1 at the power density of 810 W kg−1. Meanwhile, the capacitor showed extremely high stability due to tight anchoring of NiHCF on CNFs. This work provides a simple and versatile method to produce self-supporting MHCF@CNF composites for constructing high performance supercapacitor. [Display omitted] • A versatile method to produce various MHCF@CNF is demonstrated. • The self-supporting MHCF@CNF are extremely stable with excellent flexibility. • The MHCFs particles with small size and uniform distribution promote the charge transfer. • A super high specific capacitance of 507 F g−1 (1 A g−1) is achieved on NiHCF@CNF. • NiHCF@CNF//PCNF delivers energy density of 60 Wh kg−1 at a power density of 810 W kg−1 [ABSTRACT FROM AUTHOR]

Summary: The development of efficient methods to achieve a porous activated carbon nanostructures electrode for high‐performance electrochemical double‐layer capacitor (EDLC) is urgently needed at present. In this study, biomass‐based porous hollow carbon nanofiber/nanosheet with suitable micro/mesopores was successfully prepared using a low‐cost simple approach through chemical activation at direct pyrolysis. Biomass‐based porous carbon was performed in two different chemical activation of KOH and ZnCl2. The effects of the different KOH/ZnCl2 concentrations at high‐temperature pyrolysis on the morphological structure and porosity were investigated. The synthesized activated carbon possesses micro/mesopores hollow nanofiber/nanosheet, which enhanced specific surface area from 15.163 m2 g−1 to ultrahigh specific surface area of 1041.900 m2 g−1. These behaviors exhibit a high specific capacitance of 213 F g−1 in a two‐electrode system with excellent energy and power density of 29.6 Wh kg−1 and 106.6 W kg−1 at 1 M H2SO4 aqueous electrolyte. These results provided accurate information about a feasible approach to synthesize biomass‐based porous hollow carbon nanofiber/nanosheet to boost high‐performance energy storage devices. [ABSTRACT FROM AUTHOR]

• MnO 2 /CNF/Ag nanofabric electrodes are developed for flexible supercapacitors. • The brittle issue in the CNF electrode is greatly improved by an Ag incorporation. • The optimized MnO 2 /CNF/Ag electrode has a specific capacitance of 184 F/g at 1 A/g. • An energy density of 16.3 Wh/kg and a power density of 400 W/kg was achieved. • A capacitance retention rate of 87 % was demonstrated when subjected to bending. Flexible supercapacitors are gaining increasing popularity due to their potential in powering portable, wearable, and lightweight electronic devices. In this study, we have successfully developed a high-performance flexible electrode for quasi-solid-state supercapacitors by incorporating Ag into carbon nanofibers (CNF) through electrospinning, and growing MnO 2 as an active material on the electrode using an in-situ redox method. The Ag and MnO 2 co-decorated CNF electrode offers several advantages over conventional CNF electrodes, including an enlarged reaction area, higher charge storage capacity, and improved resistance to brittleness issues. Among all the quasi-solid-state supercapacitors tested, the MnO 2 -decorated electrode with an optimized Ag incorporation exhibited the highest specific capacitance of 184 F/g at a current density of 1 A/g, representing a remarkable 17-fold increase compared to the reference CNF electrode. Furthermore, the Ag and MnO 2 co-decorated electrode demonstrated an energy density of 16.3 Wh/kg and a power density of 400 W/kg at the same current density. Notably, the electrode exhibited excellent flexibility, with a capacitance retention rate of 87 % when subjected to bending with a curvature ranging from 5 to 1.25 cm. Our results suggest that the Ag and MnO 2 co-decorated CNF electrode holds great promise for flexible energy storage applications. [Display omitted] [ABSTRACT FROM AUTHOR]

In this study, we have successfully developed a series of low-cost, environmentally friendly, and high-performance carbon-based conductive inks with a three-dimensional micro-nano structure through a simple dispersion and ball-milling process, offering an array of desirable characteristics. Significantly, the carbon-based conductive inks remained stable even after a 30-day settling period. Furthermore, the conductive film, produced using screen printing techniques, demonstrated an impressive conductivity of 1.99 × 103 S/m. This remarkable conductivity highlights the ability of the films to consistently maintain a robust conductivity network, even when subjected to 5000 mechanical bending/releasing tests. Expanding on the success of our carbon-based conductive inks, we harnessed their potential in the production of all-solid-state flexible Micro-supercapacitors (MSCs) with an interdigital structure, utilizing screen-printing technology. The resulting MSCs exhibited outstanding performance metrics, including a notable areal energy density of 1.47 µWh cm-2 and an area power density of 0.2 mW cm-2. Moreover, these MSCs demonstrated remarkable cycle stability, retaining 96.3% of their capacitance after 20,000 cycles. Additionally, their excellent mechanical flexibility was evident as they experienced only a minor 2.98% capacitance degradation after undergoing 5000 bending/releasing cycles. These findings highlight the enormous potential of our work in facilitating the scalable production of wearable and portable electronic products. • Synthesize a high-performance aqueous carbon-based ink. • Carbon black was attached to graphite flakes to construct an effective three-dimensional micro-nano structure. • The ink was applied in the field of planar micro-supercapacitors with screen printing technology, showing good electrochemical performances and excellent mechanical flexibility. [ABSTRACT FROM AUTHOR]

The increasing commercialization of flexible electronic products has sparked a rising interest in flexible wearable energy storage devices. Supercapacitors are positioned as one of the systems with the most potential due to their distinctive advantages: high power density, rapid charge and discharge rates, and long cycle life. However, electrode materials face challenges in providing excellent mechanical strength while ensuring sufficient energy density. This study presents a method for constructing a flexible composite electrode material with high capacitance and mechanical performance by electrochemically depositing high-quality manganese dioxide (MnO 2) onto the surface of a nanocellulose (CNF) and carbon nanotube (CNT) conductive film. In this electrode material, the CNF/CNT composite film serves as a flexible conductive substrate, offering excellent mechanical properties (modulus of 3.3 GPa), conductivity (55 S/cm), and numerous active sites. Furthermore, at the interface between MnO 2 and the CNF/CNT substrate, C-O-Mn bonds are formed, promoting a tight connection between the composite materials. The assembled symmetric flexible supercapacitor (FSC) demonstrates impressive performance, with an areal specific capacitance of 934 mF/cm2, an energy density of 43.10 Wh/kg, a power density of 166.67 W/kg and a long cycle life (85 % Capacitance retention after 10,000 cycles), suggesting that they hold promise for FSC applications. [Display omitted] [ABSTRACT FROM AUTHOR]

In this work, lignin-based carbon nanofibers (LCNFs) were for the first time served as substrate for in-situ electrodeposition of polyaniline (PANI) and tested as pseudocapacitor. Two LCNFs with different lignin ratios were designed to distinguish their morphology and structural properties. Next, PANI deposition mechanisms on both LCNFs were investigated and the electrochemical performance of the resulting LCNF/PANIs were evaluated. It was found although LCNF2 was composed of less uniform nanofibers due to more presence of lignin in precursor dope, it had higher tensile strength/modulus than LCNF1 (strength: 34.3MPa to 24.2 MPa; Modulus: 2.40 GPa to 1.45GPa) and was more cost-effective. Particularly, the beaded fibers on LCNF2 contributes to the deposition of PANI with higher specific mass capacitance (612.8 F g−1 to 547.0 F g−1). Upon assembling into solid-state supercapacitors, the C m of LCNF2/PANI device was determined to be 229 F g−1 and the maximum energy density was 11.13Wh kg−1 at a power density of 0.08 kW kg−1. This work showed LCNF produced from renewable and low-cost lignin could be directly used as substrate for PANI deposition. Moreover, the composition in spinning dope played an important role in determining the performances of resulting pseudocapacitors. • First attempt to electrochemically deposit polyaniline on Lignin-based carbon fibers. • LCNF/PANI electrodes showed competitive capacitance to other non-renewable carbon-based electrodes. • LCNF/PANIs derived from beaded/non-beaded LCNFs are compared and investigated. • Higher lignin content is a merit when using as pseudocapacitor electrodes. [ABSTRACT FROM AUTHOR]

We report the microstructure, electrical and electrochemical properties of hybrid nanofibers composed of polyacrylonitrile (PAN)/lignin-derived carbon nanofibers and LaMnO3-based inorganic nanofibers for advanced applications as free-standing and binder-free electrode materials of energy storage devices. For this purpose, hybrid nanofibers are fabricated via dual-electrospinning technique and following heat-treatment at different temperatures of 700–1000 °C for simultaneous carbonization and calcination. The SEM, EDS, and XPS analyses reveal that the carbon content in the hybrid nanofibers increases with increasing the heat-treatment temperature and that La and Mn elements are dispersed uniformly over the hybrid nanofibers. The hybrid nanofibers heat-treated at 900 and 1000 °C have a high electrical conductivity of ~ 0.22 S/cm and ~ 0.35 S/cm, respectively. Accordingly, a symmetric two-electrode supercapacitor based on hybrid nanofibers heat-treated at 1000 °C is characterized to have excellent electrochemical performance such as specific capacitance of ~ 95.2 F/g at 1 A/g, power density of 667 W/kg, energy density of 17.6 Wh/kg, and capacitance retention of ~ 97% after 2000 cycles. The results denote that PAN/lignin and LaMnO3-based hybrid nanofibers can be utilized as self-supporting high-performance electrode materials for advanced energy storage devices. [ABSTRACT FROM AUTHOR]

The N‐doped porous carbon (NPC) /carbon micro‐nanotubes (CMNT) /NixCoyOz nanosheets with rich mesopores and 1.37 wt% nitrogen doping are successfully synthesized by a pyrolysis‐ionization‐precipitation combination process, using coal‐based polyaniline and nickelocene as original materials. Therein, most of the CMNT are upright CMTs and worm‐like curved CNTs, and a few are bamboo‐like tubes or carbon nanofibers. Moreover, many flower‐like aggregates assembled by spinel NiCo2O4 nanosheets are anchored on the surface of the NPC and CMNT. The NPC/CMNT/NixCoyOz exhibits a high specific capacitance and cycling stability, attributed to the large BET specific surface area (485 m2/g), suitable BET average pore size (2.3 nm), good hydrophilicity and wettability, and synergistic effects among three components. The assembled NPC/CMNT/NixCoyOz//AC asymmetric supercapacitor also demonstres a high specific capacitance of 120 F g−1 at a current density of 1 A g−1 and a high energy density of 16.7 Wh kg−1 at a power density of 500 W kg−1. [ABSTRACT FROM AUTHOR]

Herein, this paper reports a facile method to prepare electrospun carbon nanofiber mats (ECNFMs) with high specific surface area and interconnected structure using polyacrylonitrile (PAN) as a precursor and novolac resin (NOC) as a polymer sacrificial pore‐making agent. Without additional treatment, the prepared ECNFMs have a highly porous structure because NOC decomposes in a wider temperature range than most polymer activators. The NOC content in the PAN nanofibers shows important effects on porosity. The BET specific surface area of ECNFMs reaches a maximum of 1468 m2 g−1 when the precursor nanofibers contained 30 wt% NOC (ECNFM‐3) after carbonization at 1000 °C. The supercapacitor device from ECNFM‐3 electrode and all‐solid‐state electrolyte shows excellent cycling durability and high specific capacitance: ≈99.72% capacitance retention after 10 000 charge/discharge cycles and ≈320 mF cm−2 at 0.25 mA cm−2. Furthermore, it shows a large energy density of ≈11.1 μWh cm−2 under the power density of 500 mW m−2. Activation of carbon nanofibers simply by the addition of NOC into precursor nanofibers can offer a handy way to prepare ECNFMs for high‐performance all‐solid‐state supercapacitors and other potential applications. [ABSTRACT FROM AUTHOR]

Summary: With the increasing challenge of energy, resource, and environment, it is highly desired to develop renewable energy and corresponding efficient energy storage technologies basing on reproducible materials. Recently, using biomass and biotechnology to prepare electrode material for energy storage devices is gaining growing attention. Here, we use biomass, celery, as a material source and developed a new way to prepare highly qualified graphitized porous carbon. Besides, instead of direct carbonization, the celery is first freeze‐dried to protect the original elements and structure of biomass. Furthermore, to sculpture more nanoscale pores in the produced material, the following carbonization process is also greatly modified by investigating proper carbonization temperature and time. Therefore, the interconnected hierarchical porous structure can be formed based on the protected original pores with size of micrometers and the newly formed pores with size of nanometers. The resulted interconnected hierarchical porous carbon is used to prepare supercapacitor electrode and exhibit excellent energy storage properties. Without any extra activating or doping process, the specific capacitance of the resulted electrode reached 350.0 F g−1 at 1 A g−1, which is 5.28 times of that of directly carbonized material. And the power density reached 8.0 kW kg−1 with the energy density maintaining 16.3 Wh kg−1. [ABSTRACT FROM AUTHOR]

• Average diameter of SU8 polymer-derived CNF is within the range of 60–140 nm. • SU8 polymer-derived pattern CNF anodes show ultra-high capacity (3450 mA h g−1). • GED and GPDs of Li/CNF cells from DFT studies are 26.96 kW h g−1 and 26.96 kW g−1. • Average, oxidation and reduction potential of CNF/LMNC cell are 4.4, 2.44 and 2.64 V. • GED and GPDs of pattern CNF/LMNC cells are 43.18 kW h kg−1 and 51.82 kW kg−1. This study provides a novel and sustainable protocol for the synthesis of SU8 polymer-based pattern, un-pattern carbon nanofibers (CNF) using an electrospinning process followed by a photolithography technique. Scanning electron microscopy (SEM) analysis of pattern, un-pattern CNFs shows that the average diameter of CNF is within the range of 60–140 nm. Transmission electron microscopy (TEM) studies disclose the average size of CNF exists within the range of 40–150 nm. The first-principle calculations predict that the gravimetric energy and power densities of Li/CNF half cells are 26.96 kW h g−1 and 26.96 kW g−1, respectively. The corresponding theoretical volumetric energy and power densities are 0.07 W h cm−3 and 0.07 W cm−3, respectively. Electrochemical analysis demonstrates the initial discharge capacities of pattern, un-pattern Li/CNF half cells at 100 mA g−1 are 3450 and 2429.8 mA h g−1, respectively. The gravimetric energy density of pattern, un-pattern Li/CNF half cells are within the range of 1800–1366.76 W h kg−1, and subsequent power densities are in the span of 519.63–434.22 kW g−1. The theoretical gravimetric energy and power densities of CNF/LiMn 0.33 Ni 0.33 Co 0.33 (LMNC) full cells are 2.9 kWh kg−1 and ∼ 2.9 kW kg−1, respectively. Their theoretical volumetric energy and power densities are 1.96 W h cm−3 and 1.96 W cm−3, respectively. Electrochemical analysis discloses that the gravimetric energy and power densities of pattern CNF/LMNC full cells are in the range of 43.18–42.4 kW h kg−1 and 51.82–50.90 kW kg−1, respectively. The gravimetric energy and power densities of un-pattern CNF/LMNC full cells are 42.07–41.59 W h kg−1 and 50.48–49.92 kW kg−1, respectively. [ABSTRACT FROM AUTHOR]

Lithium-ion supercapacitors (LICs) have received widespread interests because of their high power density, high energy and long life characteristics. The electrodes for LICs play a significant role in enhancing their performance. Therefore, it is of great significance to design and develop high-performance electrode materials for LIC through integrating various materials to make up for each other's disadvantages. Herein, a bimetallic composite nanomaterial with hierarchical structures (CoSn X /CNFM) and a porous carbon nanomaterial with high specific surface area (PCNFM) were obtained through combining electrospinning, anion exchange or alkali etching and subsequent high-temperature carbonization, respectively. The LIC assembled with the pre-lithiated CoSn X /CNFM as anode and the PCNFM as cathode exhibited a high energy density of 41.48 Wh/kg at a power density of 1500 W/kg, and still had an energy density of 28.13 Wh/kg at a high power density of 7500 W/kg, illustrating its high power density and high energy density. Thus, this paper proposes an effective method for designing and manufacturing high-performance LICs. • Nanofibers with uniformly distributed ZIF-67 NPs were prepared in batches by EMAI. • Hierarchical-structured CoSn X /CNFM was prepared by anion exchange and carbonization. • PCNFM with high specific surface area was prepared by etching and carbonization. • A LIC with pre-lithiated CoSn X /CNFM as anode and PCNFM as cathode was assembled. • The assembled LIC had high power density and high energy density. [ABSTRACT FROM AUTHOR]

SnS is an ideal material for supercapacitors because of its unique layered structure and excellent electrochemical performance, but the research of SnS based electrode materials of flexible self-supporting supercapacitors has been rarely exploited. In this study, microsphere like Co doped SnS grown on carbon nanofibers (Co-SnS@CNF) was prepared by electrospinning, hydrothermal method and annealing treatment. Co-SnS@CNF has great flexibility, high specific capacitance, excellent rate performance and cycle stability. Specifically, the specific capacitance is 750 F g−1 at the current density of 1 A g−1. The special microsphere structure with more electrochemical active sites and lower resistance of ion and charge transfer by Co doping are responsible for the superior electrochemical performances. Furthermore, when assembled Co-SnS@CNF as the symmetrical supercapacitor device, the energy density of 20.89 Wh Kg−1 and the power density of 376 W Kg−1 are achieved at the current density of 1 A g−1, while showing ultra-high cycle stability. Therefore, the Co-SnS@CNF offers excellent application potential for flexible self-supporting supercapacitors. • Revealing reasons for the high-performance of the microspherical Co-doped SnS. • The specific capacitance is 750 F g−1 at the current density of 1 A g−1. • The assembled symmetrical device exhibits the ultra-high cycle stability. [ABSTRACT FROM AUTHOR]

Hierarchical MnO 2 -based fiber-in-tube and particle-in-tube nanostructures with unique chemical compositions and gradient pores have been rationally designed and constructed using a simple self-template method for high-performance asymmetric supercapacitors, which deliver extraordinarily excellent energy density. • MnO 2 -based fiber-in-tube and particle-in-tube nanostructures are designed. • The hierarchical architectures are fabricated via a simple self-template approach. • The novel nanotubes yield superior specific capacity as supercapacitor electrodes. • The asymmetric supercapacitors deliver extraordinarily excellent energy density. Manganese dioxide (MnO 2) promises for high-performance asymmetric suprecapacitors, owing to its high theoretical capacity, abundant source, and low cost. However, insufficient practically-achievable capacity and relatively narrow voltage window in alkaline electrolyte are blocking high energy density of MnO 2 -based supercapacitors, where strategies for activating its capacitive performance and widening voltage window are the top priorities to solve the bottleneck problems. Herein, both the fiber-in-tube (NCCM-FiT) and particle-in-tube (NCCM-PiT) nanostructures coulping active NiCoO x nanoparticles and conductive carbon with MnO 2 tubes have been purposely fabricated, using the electrospun nickel cobalt oxides/carbon nanofibers (NCO/CNFs) as the self-template agents for enhanced energy density of MnO 2 -based supercapacitors. These hierarchical hollow nanotubes with gradient pores and unique compositions yield excellent capacitive properties, in terms of a competitive capacity (431.7 F g−1 or 431.7 C g−1, 0.5 A g−1), which is 2.7 times that of the MnO 2 nanotubes-based electrodes. A maximum energy density of 46.4 Wh kg−1 is obtained at the power density of 400 W kg−1 for the asymmetric device assembled with the NCCM-PiT-based positive electrode and the electrospun CNFs-based negative electrode. The remarkable energy density demonstrated by these hierarchical hollow nanotubes exemplifies a novel and effective design in electrode materials for the asymmetric supercapacitors (ASCs) with superior performance. [ABSTRACT FROM AUTHOR]

In this paper, we proposed the synthesis of CoFe nanoparticles (NPs) which have been deposited on carbon nanofibers (CNFs) with a facile electrospinning route followed by thermal reduction. The performance of obtained CNF supercapacitors are improved from 51 to 190 F/g (247 mF/cm2) at 0.5 A/g with the combination of CoFe NPs and graphitized carbon layers The device possessed an energy and power density of 6.6 Wh/kg and 125 W/kg, respectively. Furthermore, the capacitance retention can still maintain about 96.6% after 10,000 cycle test and it is worth noting that the cycling stability is ultrahigh. This research proves that bimetallic nanoparticles embedded in CNFs can elucidate new insights into the development new nanofiber electrode materials for the next generation of symmetric supercapacitors. [ABSTRACT FROM AUTHOR]

The aim of this study is to develop the templateless fabrication of hierarchical porous carbon nanofiber (CNF)/MnO 2 composites (PMnCD) derived from polyacrylonitrile (PAN)/cyclodextrin (CD) and investigate their morphological and electrochemical properties to determine the different capabilities of inclusion complexes (ICs) formed by α-CD, β-CD and γ-CD. Among the three CD phases, the PMnCD(β) composite using β-CD exhibits a hierarchical porous structure with large specific surface area of 499 m2g-1, and total pore volume of 0.32 cm3g-1, which helps with adsorption efficiency and accumulation of hydrated molecules for double-layer formation. In addition, the numerous mesopores and nitrogen functionalities of the PMnCD(β) composite provide fast diffusion channels for electrolyte ions and higher attractive interactions with electrolyte ions through the pseudocapacitive character. As a result, the PMnCD(β) electrode has a high specific capacitance of 228 Fg-1 at 1 mAcm−2, maximum energy density of 25.3–16.0 Whkg−1 in the power density range of 400-10,000 Wkg-1, and excellent cycling stability of more than 94% after 10000 cycles in aqueous solution, thereby offering potential applications for supercapacitors. Image 1 • Hierarchical porous PMnCD is fabricated by electrospinning without a template. • β-CD stabilizes and encapsulates MnCl 2 through the good size match of β-CD and MnCl 2. • PMnCD(β) shows a large specific surface area for accumulation of ions. • Many mesopores and nitrogen groups of PMnCD(β) provide fast ion diffusion. • Hierarchical porous PMnCD(β) is applied to high-performance supercapacitors. [ABSTRACT FROM AUTHOR]

The preparation of electrode materials with superior electrochemical performance and excellent mechanical properties are essential for the fabrication of flexible supercapacitors. However, the compatibility of the porosity and flexibility for the electrode materials remains challenging. Herein, free-standing porous coaxial carbon nanofiber (PCCNF) membranes with large specific surface area (648 m2 g−1) and suitable pore size distribution were fabricated by a facile coaxial electrospinning technique and template method. PCCNF possesses superb capacitance of 261 and 48 F g−1 (1 A g−1) in three-electrode and two-electrode system, respectively, result in remarkable energy density (48.6 ± 3 Wh kg−1) and power density (67.5 ± 1 Wh kg−1). Moreover, supercapacitor devices based on PCCNF show superb flexibility as well as excellent electrochemical and mechanical stability. PCCNF-based high performance supercapacitors may be suitable for flexible electronic energy storage devices. Porous coaxial carbon nanofibers (PCCNF) with large specific surface area, well-balanced pore size distribution, and remarkable flexibility are fabricated by a facile coaxial electrospinning technique and template method. Flexible supercapacitors fabricated with the as-prepared PCCNF display superb electrochemical and mechanical stability. This work provides exciting opportunities for the preparation and application of flexible energy storage devices. Image 1 [ABSTRACT FROM AUTHOR]

Flexible supercapacitors have drawn tremendous attention resulting from the rapid development of wearable electronic devices. Herein, we develop an effective and facile two-step approach to prepare high content nitrogen, sulfur co-doped porous carbon nanofibers film as electrodes of flexible supercapacitors. Benefiting from the high specific surface area and rich nitrogen/sulfur content, nitrogen and sulfur co-doped porous carbon fibers film (N, S co-doped PCFF) electrodes exhibit a high mass specific capacitance of 307.8 F g−1, and the capacitance retains 98% of initial capacitance after 5000 cycles in a three-electrode system. The as-assembled flexible supercapacitor devices with polyvinyl alcohol/KOH gel electrolyte demonstrate a highest mass specific capacitance of single electrode of 183.9 F g-1 at the scan rate of 2 mV s-1, which is better than that of other heteroatom doping carbon materials. In addition, the energy density reaches as high as 16.35 Wh kg−1 with the power density of 147 W kg−1 and retains as 5.34 Wh kg−1 with higher power density of 2402 W kg−1. Furthermore, the flexible devices show good cycling stability, superior flexibility and stable electrochemical performance. Schematic demonstration of Nitrogen, Sulfur co-doped PCFF electrodes, and schematic structure of flexible all-solid-state supercapacitor. Image 1 [ABSTRACT FROM AUTHOR]

• α-Ni(OH) 2 nanobristles on HPCNFs are achieved by bio-mediated synthesis method. • Eggshell membrane-mediated method is beneficial to ion diffusion. • The Ni(OH) 2 /HPCNFs composites exhibit a superior capacity performance. • The Ni(OH) 2 /HPCNFs//AC ASC device possesses high energy and power density. Nickel hydroxide nanobristles were fabricated on the surface of hollow carbon nanofibers (HPCNFs) through a low cost and effective bio-mediated technology, where the eggshells with eggshell membrane were selected as multifunctional reactors to separate the precursor solution to control OH− ion diffusion in order to form α-Ni(OH) 2 instead of β-Ni(OH) 2. The as prepared Ni(OH) 2 /HPCNFs displays high capacity (283 mAh/g) and a remarkable cycle life (82% specific capacity retained after 5000 cycle numbers) in 1M KOH aqueous solution. Compared with literature reports, in which Ni(OH) 2 are often considered for pseudocapacitors, we suggest our electrodes are good for rechargeable alkaline secondary batteries or as battery electrodes in hybrid supercapacitors, based on battery behavior observed in our electrochemical measurements. As battery electrodes in hybrid supercapacitors, an asymmetric supercapacitor was fabricated, in which Ni(OH) 2 /HPCNFs and activated carbon as positive and negative electrode, respectively (Ni(OH) 2 /HPCNFs//AC ASC), which displays intriguing electrochemical performances with a high energy density (31.3 Wh /kg at 300.5 W/ kg). The results demonstrate that the bio-mediated method for achieving Ni(OH) 2 /HPCNFs nanomaterials is becoming a promising technology in alkaline batteries. [ABSTRACT FROM AUTHOR]

Recently, Li-ion capacitor as a kind of novel energy storage device with high energy density and power density have caused wide concern. In this study, the porous carbon nanofiber/molybdenum disulfide nanoflake-flowerballs composite material is successfully prepared via hydrothermal method using the three-dimensional porous carbon nanofibers as a carrier. The molybdenum disulfide nanoflake-flowerballs are uniformly distributed and fill in three-dimensional porous carbon nanofibers skeleton, and the clear composite material with nanofiber morphology is formed. This material presents moderate specific surface area (81.67 m2 g−1) and good electrical conductivity (22.32 S cm−1) and is used as the anode in the Li-ion capacitor, and the big energy density at high power density (the energy density could reach 75.5 Wh kg−1 and 22.5 Wh kg−1 at power densities of 0.075 kW kg−1 at 30 kW kg−1, respectively) are achieved, which has broad application prospect in the energy storage field. • The three-dimensional PCNF loading MoS 2 nanoflake-flowerballs was constructed. • The MoS 2 nanoflake-flowerballs inner nanofibers provide the large reaction area. • The three-dimensional PCNF skeleton offers conductive path. • The 3D-PCNF/MoS 2 -NFFBs used as the anodes of LICs exhibit excellent properties. [ABSTRACT FROM AUTHOR]

The dramatic development of wearable electronics has led to extensive research into flexible supercapacitors as wearable energy storage devices. The practical application of supercapacitors to wearable electronics requires improved temperature tolerance and high energy density. Herein, we report the fabrication of a high-voltage flexible aqueous supercapacitor featuring high energy density and a wide operating temperature range. This is achieved by the strategy of simultaneously utilizing asymmetric electrodes and water-in-salt gel electrolyte (WISGE). Using NaClO 4 -based WISGE and asymmetric electrodes consisting of Na-inserted MnO 2 and N-doped carbon nanofibers, we obtain excellent electrochemical performance, including a gravimetric capacitance of 97.2 F g−1, energy density of 90 Wh kg−1, power density of 28.1 kW kg−1, operation voltage window of 2.6 V, and capacitance retention of 85.2% over 10,000 charge/discharge cycles. The fabricated flexible supercapacitor is stable under repeated temperature changes between − 20 and 80 °C, regardless of bending deformation. After three cycles of cooling and heating, the initial capacitance at room temperature is 95.1% recovered. This study demonstrates the potential application of our high-performance flexible aqueous supercapacitors to wearable devices, given their resistance to changes in environmental temperature and mechanical deformation. [Display omitted] • Supercapacitor consists of the asymmetric electrode and water-in-salt gel electrolyte. • Supercapacitor exhibits wide voltage window (2.6 V) and temperature range (−20 to 80 ℃). • The initial performance was maintained even after repeated temperature changes. • Performance is stable under repeated bending deformation over wide temperature ranges. [ABSTRACT FROM AUTHOR]

Nowadays, materials that possess high activity and natural oxygen vacancy have garnered significant attention as potential electrode materials for supercapacitors. In this study, we successfully prepared the Hf 6 Ta 2 O 17 (HTO) nanofibres (NFs) with an orthorhombic superlattice structure using the electrospinning technique and sintering process. The characterization results indicate that the HTO NFs synthesized at 750 °C show good micro nanostructures and outstanding electrochemical properties. To enhance its energy storage performance, additional oxygen vacancies (OVs) were introduced through a carbothermal treatment under an Ar atmosphere. Although longer reduction reaction times can produce more OVs, the integration of grain boundaries and the growth of grain size caused by large annealing times may limit its electrochemical performance. Therefore, the HTO NFs treated for 1 h (HTO/C-1) exhibited the maximum C s of 925 F·g−1 at 1 A·g−1 with a larger voltage window of 2.1 V. Furthermore, a symmetric supercapacitor fabricated by two reduced HTO NFs electrodes and 1 M Na 2 SO 4 solution, recorded as r-HTO NFs//r-HTO NFs. The device demonstrated excellent energy density of 73.3 Wh·kg−1 (at power density of 1050 W·kg−1) and a long cycling life (81.8% retained after 5000 cycles). These results suggest that the optimized reduction process can provide appropriate oxygen vacancies in HTO NFs, thereby effectively enhancing its performance. [Display omitted] • The Hf 6 Ta 2 O 17 (HTO) nanofibres (NFs) are synthesized by electrospinning method. • The micro nanostructures and electrochemical property of HTO NFs can be designed by controlling the synthesis temperature. • The carbothermal treatment carried under Ar atmosphere is used to improve the amount of oxygen vacancies of HTO NFs. • The HTO NFs treated of 1 h (HTO/C-1) presents excellent capacitance of 925 F·g−1 at 1 A·g−1. • The r-HTO NFs//r-HTO NFs device shows high energy density of 73.3 Wh·kg−1 at power density of 1050 W·kg−1. [ABSTRACT FROM AUTHOR]

ZIF derived selenides have become a promising battery-type electrode material, but pure ZIF derived materials tend to agglomerate, averting active sites from full exposure. Herein, a hierarchical Co doped Ni 3 Se 4 on carbon nanofibers modified by ZIF-67 was fabricated by co-electrospinning, calcination and solvothermal synthesis, whose mass ratio of ZIF-67 to PAN and the type of chalcogenides were regulated. Among them, CNF-Co(1:1)@NiSe, with the feature of battery-type materials, displayed the large specific capacitance of 749.27 F g−1 at 0.5 A g−1 and superb rate performance when the current density increased from 0.5 to 10 A g−1, owing to its unique hierarchical structure along with synergistic effect of Co-doped Ni 3 Se 4 , Co-N-C, and CNF. Notably, a solid-state hybrid supercapacitor (CNF-Co(1:1)@NiSe//active carbon) was build, and delivered the maximum energy density of 32.36 Wh kg−1 at 1 A g−1 along with the maximum power density of 7999.99 W kg−1 at 10 A g−1. In addition, the supercapacitor exhibited excellent cycle stability during 5000 cycles and was successfully used for the luminescence of LED, revealing a good application prospect for CNF-Co(1:1)@NiSe. [ABSTRACT FROM AUTHOR]

[Display omitted] • Hollow N -rich multilayered CNFs are prepared by sequential electrospinning. • The top-layer PAN/urea-based CNF acts as charge storage and pseudocapacitance. • The interlayer PMMA-based CNFs with tubular structure promote charge transport. • The bottom layer of PAN-based CNFs with numerous micropores provides charge storage. N -rich multilayered carbon nanofibers with hollow channels (PPMPN) are fabricated to fully utilize the mesopores, micropores, and nitrogen-functional groups of carbon nanofibers (CNFs) for superior electrochemical properties. Among all composites, the PPMPN(10) exhibits high specific surface area (570 m2g−1) with mesopore volume fraction (42%) and rich surface functionalities (∼7.25at% nitrogen and ∼ 16.1at% oxygen), helping to improve electrochemical performance. The performance of the symmetric supercapacitor of the PPMPN was significantly improved in terms of its specific capacitance of 189 Fg−1 at 1 mAcm−2, good retention of 80% (when the current density is increased from 1 to 20 mAcm−2), energy density of 23.5 Whkg−1 at a power density of 400 Wkg−1, and cycling stability of 94% for 10,000 cycles. The top layer plays a role in charge storage/transport by increasing electrical conductivity due to N -functional groups. The intermediate layer with tubular 1D nanostructures enhances the diffusion of electrolyte ions even at higher current densities. The bottom layer composed of numerous micropores serves as a charge storage layer. Therefore, in the multilayer CNF, the micropores/mesopores and N -functional properties of each layer do not interfere with each other, and the advantages of the factors of each layer are maximized in the electrochemical properties. [ABSTRACT FROM AUTHOR]

• LrGO/Co/CoO interdigital electrodes for MSCs were prepared via laser direct writing. • The specific capacitance of LrGO/Co/CoO-based MSCs increases with decreasing laser writing speed. • LrGO/Co/CoO-based MSCs exhibit excellent electrochemical performance. • LrGO/Co/CoO-based MSCs exhibit good mechanical flexibility. Graphene/CoO nanocomposites have excellent electrochemical performance and are extensively applied to microsupercapacitors (MSCs). Herein, we propose a simple and efficient method for laser direct writing on a graphene oxide/Co(CH 3 COO) 2 precursor to process graphene/Co/CoO nanocomposite interdigital electrodes for MSCs. This work investigates the structural defects, crystal structure, sheet resistance, elemental composition, and bond characteristics of graphene/Co/CoO nanocomposites synthesized at different laser writing speeds. The specific capacitance, power density, and energy density of the prepared MSC based on PVA/H 3 PO 4 electrolyte and graphene/Co/CoO interdigital electrodes reach 420.23 mF cm−2 (48.31 F cm−3), 1.97 mW cm−2 (226.43 mW cm−3), and 58.37 μWh cm−2 (6.71 mWh cm−3), respectively. Moreover, the Coulombic efficiency and capacitance retention rate of the prepared MSC after 10,000 cycles are 97.97% and 86.56%, respectively. The charge storage of the prepared MSC is mainly achieved through diffusion-controlled intercalation reactions. In addition, the prepared MSC shows good mechanical flexibility. [ABSTRACT FROM AUTHOR]

Flexible electrode materials have achieved great breakthroughs during the past decades. However, many challenges remain such as how to overcome the frangibility and enhance the flexibility, and advance the high specific capacitance. We fabricated a free-standing, foldable, and conductive cellulose acetate (CA)-based metal-organic framework (MOF) composites by facile electrospinning carbonization and co-precipitation method. The sustainable cellulose derivative provides a flexible matrix, which contains hierarchically porous and ample redox activities. The intermolecular interaction is enhanced for coordination between exposed hydroxyl on deacetylated CA and metal ions, thus reduce the fracture of the CA nanofibers. Importantly, multi-layer heterojunction structure and honeycomb-like MOF nanosheets with reversibly flexible deformation create interlamellar pathways to improve the bending resistance of nanofibers. The controlled Co/Zn ion concentration could effectively modulate spatial distribution of Co/Zn MOF to thus generate different conductive channels. The asymmetric flexible supercapacitor based on Ni/Co LDH@ Co/Zn NC@CDCP-N electrode material gives high specific capacitance (175.2 F g−1 at 1 A g−1) and outstanding energy density (54.8 W h kg−1) at high power density (985.5W kg−1). Our work paves a way to facile fabrication of flexible and free-standing electrode materials for practical flexible energy storage, such as artificial electronic skin and soft wearable electronics. [Display omitted] • Electrospun CA-based MOF derivative possess hierarchical and hollow structure. • The CA-based MOF derivative possesses high active sites and specific surface area. • The CA-based MOF derivative exists high multiple folding ability and flexibility. • The CA-based MOF derivative is utilized as free-standing electrode material. • The FASCs delivers remarkable energy density and power density. [ABSTRACT FROM AUTHOR]

This work constructs a 1D hollow particle-based carbon nanofibers (HCNFs) derived from Zn-based metal-organic-frameworks (MOFs) particles embedded in biomass-based electrospinning nanofibers as high-performance supercapacitor (SC) electrodes. Abundant mesopores are introduced by the pyrolysis of MOFs, which generates uniformly distributed electrolyte storage pools for a fast electrolyte ions channel. Owing to its uniquely hierarchical pore structure, the derived HCNFs exhibit much enhanced supercapacitive performance. The prepared HCNF-1000 electrode has not only a high specific capacitance (229.6 F g−1 at a current density of 2 A g−1) but also good rate performance (176.8 F g−1 at 10 A g−1, 99.1 F g−1 at 30 A g−1). The two-electrode symmetrical system HCNF-SC has an energy density of 5.1 Wh kg−1 when the power density is 0.5 kW kg−1. HCNF-1000-based solid-state supercapacitor HCNF-FSC shows good electrochemical performance even in different folded states, displaying the potential application value for the development of portable wearable devices. [Display omitted] • The hollow lignin-derived carbon fibers (HCNFs) enhance electrolyte ion transfer. • The rate capability is improved by the abundantly hierarchical pores of HCNFs. • The flexible HCNF-FSC shows promising potential in powering wearable electronics. [ABSTRACT FROM AUTHOR]

Li-ion capacitor as a kind of new-style energy storage devices has attracted growing attention due to its high power and energy density. In this study, the stereoscopic honeycomb-like porous carbon nanofiber (PCNF) was used as a carrier of TiO 2 nanoparticles via simple immersion and calcination. The equally distributed anatase TiO 2 nanoparticles filling in the stereoscopic honeycomb-like PCNF skeleton provided large reaction sites, and the stereoscopic honeycomb-like PCNFs acting as support materials offered shorter electrical paths. The composite material presented unique fiber morphology, high specific surface area (268.32 m2g-1) and preferable electrical conductivity (1.31 S cm−1) which was used as an anode in Li-ion capacitor, and the large energy density versus power density (69.46 Wh kg−1 at 0.15 kW kg−1, 18.33 Wh kg−1 at 30 kW kg−1) and good cycle stability (retains 79.4% after 4000 cycles at 1 A g−1) were achieved, which had broad application prospect in the energy storage field. • A stereoscopic honeycomb-like PCNF loading TiO 2 nanoparticles material is designed. • The TiO 2 nanoparticles uniformly distribute and fill in stereoscopic carbon skeleton. • The stereoscopic honeycomb-like PCNF skeleton offers electrical conductivity to TiO 2. • The LIC with TiO 2 @PCNF anode exhibits good electrochemical properties. [ABSTRACT FROM AUTHOR]

Graphical abstract Highlights • Hyperporous carbon nanofibers are obtained from hypercross-linked polymers. • Arrays of porous 2D copper cobalt oxide is prepared by hydrothermal method. • Aforesaid electrode materials is used for asymmetric supercapacitor (ASC) assembly. • Assembled CCO-NS//HCP-CNF ASC device showed an ultra-high energy and power density. • The novel ASC device showed a good stability with 91.1% retention after 5000 cycles. Abstract This paper reports the fabrication of an ultra-high energy and power density asymmetric supercapacitor (ASC) containing a novel porous carbon nanofiber derived from hypercross-linked polymers (HCP-CNF) and two-dimensional copper cobalt oxide nanosheets (CCO-NS) as the negative and positive electrodes, respectively. The micropore-enriched HCP-CNF is obtained from a facile Friedel-Crafts reaction with naphthalene and α, α′-dichloro- p -xylene as the starting material. The CCO-NS have been prepared by a simple and inexpensive hydrothermal synthesis using polyvinylpyrrolidone (PVP) as a shape controlling agent. The fabricated CCO-NS//HCP-CNF ASC device exhibit a high specific capacitance, 244 F g−1 at a current density of 1 A g−1, owing to the unique porous architecture of CCO-NS and the interconnected microporous carbon skeleton with a high surface area of HCP-CNF. Furthermore, the assembled ASC device show an ultra-high energy density of 25.1 Wh kg−1 at a power density of 400 W kg−1 with maximum operating voltage of 1.60 V. The electrode shows good capacitance retention (91.1%) after 5000 cycles in a 3 M aqueous KOH solution. In addition, two ASC devices are connected in series powered a 5 mm diameter LED indicator for approximately 30 min, highlighting its efficient power supply. [ABSTRACT FROM AUTHOR]

α-MnO 2 nanorods have been grown on the surface of carbon nanofibers (CNFs) for enhancing the electrical conductivity of MnO 2. We have synthesized α-MnO 2 /CNF (0–5 wt%) nanocomposites using a co-precipitation method. The x-ray diffraction results confirm the formation of a single phase α-MnO 2 and SEM/TEM images reveal the formation of α-MnO 2 nanorods, whose size depends on the amount of CNF in the nanocomposite. Both the surface area and electrical conductivity of nanocomposites are found to be strongly influenced by the presence of CNF. While α-MnO 2 /CNF(1.25 wt%) exhibits the largest surface area (381 m2/g) and only a modest increase in the electrical conductivity compared to pure α-MnO 2 nanorods, the α-MnO 2 /CNF(5 wt%) shows the least surface area (131 m2/g) but an order of magnitude higher electrical conductivity (0.67 S/cm). Cyclic voltammetry measurements show improved performance (higher specific capacitance and better cyclic stability) in all α-MnO 2 /CNF supercapacitors compared to that of pure α-MnO 2. Ragone plot shows that although α-MnO 2 /CNF(1.25 wt%) exhibits the highest specific capacitance (313 F/g at 1 A/g) and hence the highest energy density of 32.8 Wh/kg, it has the least power density of 4250 W/kg. On the other hand, α-MnO 2 /CNF(5 wt%) shows the least energy density of 7.9 Wh/kg but with a higher power density of 8478 W/kg compared to α-MnO 2 /CNF(1.25 wt%). Our studies demonstrate that one can optimize both energy and power densities by controlling the amount of CNF in the nanocomposites. Image 1 • Crystalline α-MnO 2 nanorods were grown on the surface of carbon nanofibers (CNF). • α-MnO2 nanorods size depends on the amount of CNF in nanocomposite. • α-MnO2/CNF supercapacitors showed improved performance than α-MnO 2. • Energy and power densities can be optimized by controlling the amount of CNF. [ABSTRACT FROM AUTHOR]

3D hierarchical nanocomposites always lead to excellent electrochemical properties. In this research, we have successfully designed and synthesized a hierarchical three-dimensional cobalt sulfide encapsulated carbon nanotube/carbon nanofiber (Co9S8@CNT/CNF) composite, resulting in a high-performance supercapacitor with an unrivalled capacitance of ≈1580 F g−1 at a current density of 1 A g−1. An asymmetric supercapacitor (ASC) based on these 3D hierarchical Co9S8@CNT/CNF composites exhibits a maximum energy density of 58 W h kg−1 at a power density of 1000 W kg−1 and maintains it at 38 W h kg−1 at a higher power density of 16.7 kW kg−1. Even after 10 000 charge/discharge cycles, the ASC still retains 93% of the initial capacitance at a current density of 5 A g−1. A large number of aligned CNF nanochannels combined with the synergistic effects of cobalt sulfide nanowires encapsulated in CNTs obviously accelerates the ion transfer speed and shortens the ion transfer distance, thereby boosting both power density and energy density. [ABSTRACT FROM AUTHOR]

[Display omitted] • The active sites-rich Ni-Co-P@C/Ni-B material enables fast transfer of electron/ion. • DFT results verify stable OH* adsorption energy and metallic nature of the hybrid. • The Ni-Co-P@C/Ni-B shows a high specific capacity of 306 mAh g−1 at 3 mA cm−2. • Highly porous N-doped C nanofibers with nanocages was made as negative electrode. • The hybrid supercapacitor device shows 68.3 Wh kg−1 energy density at 472 W kg−1. In recent times, a lot of research effort has been performed to develop hybrid supercapacitors (HSCs) because of their ability to produce high energy density as well as superb power density. The key issue for realizing high-performance HSCs is to minimize the kinetic mismatch between rapid capacitor-type anode and sluggish battery-type cathode. Optimizing the interface, morphology and microstructure of the electrode material is a favorable approach to surmount kinetic imbalance. Herein, a core–shell nanoarrays of ultrathin carbon layer-coated crystalline Ni-Co-phosphide (Ni-Co-P@C) and amorphous Ni-boride (Ni-B) is fabricated on a nickel foam substrate as a positive electrode material (Ni-Co-P@C/Ni-B). Theoretical analyses validate the best metallic characteristic and most stable OH* absorption energy for Ni-Co-P@C/Ni-B, which enhance its charge storage performance than analogous Ni-Co-P and Ni-Co-P/Ni-B. The porous nitrogen (N)-doped carbon (C) nanofibers consisting of tightly embedded metal–organic framework (ZIF-8)-derived interconnected N-C nanocages (HP-N-CFs) showed excellent charge storage kinetics as a negative electrode. The battery-type Ni-Co-P@C/Ni-B electrode revealed a specific capacity of 306.2 mA h g−1 at 3 mA cm−2, while highly porous capacitive HP-N-CFs electrode showed the highest capacity of 56 mA h g−1 at 2.5 mA cm−2. In addition, the assembled quasi-solid-state (Ni-Co-P@C/Ni-B//HP-N-CFs) HSCs exhibited the highest energy density of 68.3 W h kg−1 at a power density of 472 W kg−1 with a superb rate capability (68% at 50 mA cm−2) and decent cyclic durability (90% retention over 10,000 cycles). [ABSTRACT FROM AUTHOR]

The binder-free supercapacitors were fabricated from polyaniline (PANI)@MnO 2 @flexible carbon nanofibers (CNFs) composite flexible electrodes. The flexible electrodes were constructed using a layer-by-layer synthetic strategy: a large-area MnO 2 ultrathin nanosheets firstly grew onto the surface of CNFs by self-decomposition of KMnO 4 , and then the PANI was in-situ coated on MnO 2 ultrathin nanosheets in turn through a dilute-solution polymerization to form PANI@MnO 2 @CNFs ternary electrode. In PANI@MnO 2 @CNFs electrode, the two-dimensional sheet-like structure provided by the PANI@MnO 2 nanosheets could be served as a high specific surface area and electrically conductive network for fast transport of electrolyte ions and electrons in the reaction, where PANI and MnO 2 were high-performance supercapacitor electrode materials. The specific capacitance of single PANI@MnO 2 @CNFs electrode was 654 F/g at the scan rate of 10 mV/s in Na 2 SO 4 electrolyte, and the capacitance retention was about 88.8% after 1000 cycles. Furthermore, the as-prepared symmetric supercapacitor with a PVA/Na 2 SO 4 gel electrolyte exhibited the maximum energy density of 27.9 Wh/kg at the power density of 400 W/kg, which was superior or similar to previously reported values of PANI-based supercapacitor. The as-prepared supercapacitors exhibited good electrochemical performance and high flexibility, which was a meaningful exploration for the application of flexible electrodes in the production of multi-element electrode materials for supercapacitors. The binder-free supercapacitors were fabricated from polyaniline(PANI)@MnO 2 nanosheets@flexible carbon nanofibers (CNFs) composite electrodes. The specific capacitance of single PANI@MnO 2 @CNFs electrode was about 654 F/g at scan rate of 10 mV/s in Na 2 SO 4 electrolyte, and the capacitance retention was about 88.8% after 1000 cycles. Furthermore, the as-prepared symmetric supercapacitor with a PVA/Na 2 SO 4 gel electrolyte exhibited the maximum energy density of 27.9 Wh/kg at the power density of 400 W/kg. [Display omitted] [ABSTRACT FROM AUTHOR]

Low-cost, high-performance electrodes are highly attractive for practical supercapacitor applications. MnO 2 -deposited carbon nanofiber mats (MnO 2 -CNFMs) are prepared for use as binder-free supercapacitor electrodes. MnO 2 is deposited on the mats in situ by hydrothermally decomposing aqueous KMnO 4 , leading to the formation of nanocrystals of MnO 2 . The MnO 2 -CNFM electrode produced with 38.0 μmol KMnO 4 (this electrode) shows a high specific capacitance of ~171.6 F·g −1 at a scan rate of 5 mV·s −1 . Moreover, a symmetric supercapacitor with the electrode exhibits a specific capacitance of 67.0 F·g −1 , an energy density of 6.0 Wh·kg −1 and a power density of 160 W·kg −1 at a special current of 0.1 A·g −1 . Further, the symmetric supercapacitor displays excellent cycling stability, retains approximately 99% of the capacitance after 1000 cycles. The simplicity and ease of preparation of the MnO 2 -CNFMs as well as their suitability for use in coin-type supercapacitor cells make them ideal for application in cost-effective and high-performance electrodes for supercapacitors. [ABSTRACT FROM AUTHOR]

Here, core-shell supercapacitor electrodes with high performance were prepared using electrospinning, carbonation, nitrogen-doping and chemical polymerization. The core of the electrode was a N-doped porous carbon nanofiber skeleton, its shell was a conductive polymer loaded on it. The effects of pore-forming agent content, N-doped amount, and polymerization temperature on the morphologies, structures and electrochemical performance of products in each stage were characterized, and the optimum parameters were obtained. As a freestanding electrode, the SC of core-shell composite reached 342.13 F g−1 at 1 A g−1, and its SC attenuation was only 4.6 % after 1000 cycles, indicating its good charge storage performance and cycle stability. Then a symmetric supercapacitor fabricated with the best electrode displayed an energy density of 3.10 Wh kg−1 at a power density of 50 W kg−1. Therefore, this paper proposed an effective method for developing multifunctional electrode materials of supercapacitors. [Display omitted] • A core-shell composite for high-performance supercapacitor electrode was prepared. • The core layer of the composite was the N-doped porous carbon nanofiber skeleton. • The shell layer of the composite was the polypyrrole loaded on the skeleton. • The core-shell composite electrode showed excellent electrochemical performances. • An asymmetric supercapacitor device was fabricated using the core-shell electrode. [ABSTRACT FROM AUTHOR]

The composites of transition metal oxide and carbon nanofibers (CNF) are promising electrode materials for supercapacitors in alkali solutions. However, the weak binding and unsatisfactory rate performance limit their application. To improve the weak binding, this study prepared the SiO 2 -modified carbon nanofibers (Si 1 -C) via electrospinning. Then the fully encapsulated CoO-NiO (NiCo@Si 1 -C) was fabricated on Si 1 -C by solvent-thermal and calcination. As is revealed, CNF containing SiO 2 is conducive to forming a full coverage of CoO-NiO coating with a stacked petal structure. More importantly, nano-SiO 2 plays the anchoring role of NiO-CoO and CNF, making the combination more firmly. The NiCo@Si 1 -C delivers a specific capacitance of 518.1 F g−1 at 0.5 A g−1, almost 2.25 times that of NiCo@Si 0 -C (229.9 F g−1 at 0.5 A g−1). When the current density increases to 50 A g−1, it is only 3.9 % lower than the capacitance (497.9 F g−1), which means a high rate performance. Moreover, asymmetric supercapacitor devices are assembled with activated carbon (NiCo@Si 1 -C//AC) with an energy density of 11.7 Wh kg−1, even at a high power density of 14,000.7 W kg−1. [Display omitted] • Nano-SiO 2 plays the anchoring role of NiO-CoO and CNF, making the combination more firmly. • The NiCo@Si 1 -C has a unique all-encapsulated CoO-NiO with a stacked petals structure. • The NiCo@Si 1 -C has ultra-high rate performance. [ABSTRACT FROM AUTHOR]

[Display omitted] • Mn-doped PAN nanofibers were decorated with ZIF-67. • Oriented attachment of PVP/ZIF-67 occurred on Mn-doped PAN-2MI nanofibers. • PVP/ZIF-67/Mn-fibers carbonized at 900 ℃ resulted in flexible C/Co-CoO x /Mn-CNF. • The areal capacitance of 1263 mF·cm−2 was obtained at a current density of 0.25 mA·cm−2. • The energy density of 0.18 mWh·cm−2 was obtained at a power density of 0.5 mW·cm−2. Electrodes for flexible supercapacitors were fabricated from manganese-doped carbon nanofibers (Mn-CNF) decorated with carbon-coated Co-CoO x (C/Co-CoO x) nanotubes. The Mn-doped polyacrylonitrile (PAN)–2-methylimidazole (2MI) solution was electrospun using optimized Mn concentrations and ZIF-67 was then surface loaded by wet impregnation with added polyvinylpyrrolidone (PVP). These ZIF-67 loaded Mn-fibers, when annealed, resulted in carbon-coated C/Co-CoO x nanotubes on the Mn-CNF surface. In the presence of PVP, ZIF-67 oriented attachment occurs, forming evenly dispersed CoO x particles even after high temperature annealing. XRD spectra exhibit the formation of metallic Co nanoparticles (NPs), whereas Raman spectra and XPS indicate Co particle oxidation. A carbon coating limits the oxidation of Co; thus, the particles are called C/Co-CoO x. A symmetric supercapacitor cell prepared using the CNFs decorated with C/Co-CoO x using an aqueous electrolyte has a capacitance of 1263 mF⋅cm−2 at a current density of 0.25 mA⋅cm−2 and a wide potential window of 1.4 V for the optimal case. Long-term cycling showed 110 % capacitance retention after 10,000 cycles. Moreover, bending tests and powering LEDs demonstrated the flexibility and improved charge storage of the prepared nanofiber electrodes. [ABSTRACT FROM AUTHOR]

Designing cathode and anode materials that can accommodate capacity and rate performance is a significant challenge in developing lithium-ion capacitors (LICs). Herein, we synthesize a unique N/S dual-doped hierarchical porous carbon (NSC) under the effect of pore distribution modification and heteroatom doping. The nanosheet shape and pore distribution of NSC are highly adjustable, while it demonstrates a reversible capacity that is tens of times more than that of unaltered pristine active carbon. Meanwhile, the prepared glycerol-engineered polyacrylonitrile nanofiber (GPN) form a fast conducting network in the presence of glycerol and carbon nanotubes (CNTs) and exhibit a 300% higher capacity compared to pure polyacrylonitrile nanofibers at 5 A g−1. On this premise, the constructed highly stable LIC (NSC//GPN x @CNTs) can achieve an energy density of 131.48 Wh kg−1 and have an excellent capacity retention rate (93.5%) over 10,000 cycles at a high current density (5 A g−1). This work may lead to new avenues for the preparation of heteroatom-doped porous carbon and redefine the electrode matching of highly stable LICs. [Display omitted] • Highly tunable pore distribution and nanosheet shape of porous carbon. • The cathode nanofibers exhibit high electrical conductivity. • The LIC achieves high energy density and high power density simultaneously. [ABSTRACT FROM AUTHOR]