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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]

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]

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]

To develop economical and high-performance supercapacitor electrodes in an aqueous electrolyte, polyacrylonitrile (PAN)/pitch/lignin-based carbon nanofibers (CNFs) with ZnO (PPL-Zn) are successfully fabricated by one-step electrospinning of PAN, pitch, lignin, and zinc acetate. The oxygen-rich lignin in the PPL-Zn electrodes induces porosity on the fiber surface by eliminating many functional groups such carboxylic, carbonyl, hydroxyl and ketone and organic moieties in the simple heat treatment without any activation agent/activation process. Moreover, the many aromatic components, high carbon content, and low glass transition temperature of lignin are excellent precursors to CNF composites. In addition to lignin, pitch is used as a precursor to CNF to reduce the cost and increase the carbon yield and electrical conductivity of the CNFs. These characteristics afford PPL-Zn(5) (5 wt% of zinc acetate relative to PAN and lignin) with good capacitive behavior for application as supercapacitor electrodes with a maximum specific capacitance of 165 Fg-1 at 1 mAcm−2 with a capacitance retention of 88%, high energy densities of 22–18 Whkg−1 in the power density range of 400 to 10,000 Wkg-1, and excellent cycling performance reduced by only ∼6% after 3000 cycles of charge/discharge due to the synergistic effect of the electrical double layer and the pseudocapacitive effect. Image 107 [ABSTRACT FROM AUTHOR]