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A series of core-triple-shelled GCNF/PANI/NCO nanostructures have been fabricated via a facile strategy. Taking full advantage of the free-standing architecture of graphene-coated electrospun carbon nanofibers (GCNF), high conductivity and flexibility of the polyaniline (PANI) layers, and abundant active sites of nickel carbonate hydroxide (Ni 2 (CO 3)(OH) 2) nanosheets, the optimal electrode exhibits a high specific capacitance of 1565F g−1 at 1 A/g, which exceeds almost all of the reported nickel carbonate hydroxide-based electrodes in literatures. A hybrid supercapacitor delivers a high energy density of 35.4 Wh kg−1@750 W kg−1 and a long cycle lifespan. This strategy enables the controllable synthesis of core-triple-shelled hierarchical materials applicable to diverse electrochemical applications. [Display omitted] • We prepared the core-triple-shelled GCNF/PANI/NCO fiber-based films via a new route. • The optimal electrode exhibits high electrochemical properties via joint actions. • A hybrid supercapacitor displays large specific capacities and high energy density. • This strategy provides a new way to synthesize other core-triple-shelled materials. Designing novel efficient electrode materials with controlled hierarchical structure and composition for advanced supercapacitors remains a great challenge. Herein, a core-triple-shelled hierarchical GCNF/PANI/NCO nanostructure has been designed and fabricated by sequential growth of the conductive polyaniline (PANI) layers and nickel carbonate hydroxide (Ni 2 (CO 3)(OH) 2) nanosheets on the graphene-coated electrospun carbon nanofibers (GCNF) via a facile wet-chemical strategy. Taking full advantage of the free-standing architecture of graphene-coated electrospun carbon nanofibers, high conductivity and flexibility of the PANI layers, and abundant active sites of Ni 2 (CO 3)(OH) 2 nanosheets, the optimal GCNF/PANI/NCO (2 h) electrode exhibits a high specific capacitance of 1565F g−1 at 1 A/g and enhanced rate capability, which are higher than those of the GCNF, GCNF/PANI, and GCNF/NCO (2 h) electrodes at the same situation, and also exceeds most of the reported nickel carbonate hydroxide-based electrodes in literature. The superior performance should be mainly ascribed to the collaborative contribution of each component. Moreover, a self-assembled GCNF/PANI/NCO//AC hybrid supercapacitor delivers a high energy density of 35.4 Wh kg−1@750 W kg−1 and a long cycle lifespan. This strategy enables the controllable synthesis of core-triple-shelled hierarchical materials applicable to advanced electrochemical applications. [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]

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]