Nitrogen-doped graphene nanoribbon (N-GNR) nanomaterials with different nitrogen contents have been facilely prepared via high temperature pyrolysis of graphene nanoribbons (GNR)/polyaniline (PANI) composites. Here, the GNRs with excellent surface integration were prepared by longitudinally unzipping the multiwalled carbon nanotubes. With a high length-to-width ratio, the GNR sheets are prone to form a conductive network by connecting end-to-end to facilitate the transfer of electrons. Different amounts of PANI acting as a N source were deposited on the surface of GNRs via a layer-by-layer approach, resulting in the formation of N-GNR nanomaterials with different N contents after being pyrolyzed. Electrochemical characterizations reveal that the obtained N8.3-GNR nanomaterial has excellent catalytic activity toward an oxygen reduction reaction (ORR) in an alkaline electrolyte, including large kinetic-limiting current density and long-term stability as well as a desirable four-electron pathway for the formation of water. These superior properties make the N-GNR nanomaterials a promising kind of cathode catalyst for alkaline fuel cell applications.

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Anisotropic electrically conductive films (PI-GNR/CNT) consisting of highly aligned polyimide (PI) composite fibers with graphene nanoribbon (GNR) and carbon nanotube (CNT) (GNR/CNT) hybrids as nanofillers have been prepared by electrospinning. The GNR/CNT hybrids used here were prepared by one-step partial unzipping of multi-walled CNTs, in which, with the residual CNTs bonded on the randomly arranged GNR sheets, not only the aggregation of GNR sheets was greatly prevented but also an electrically conductive pathway with good conductivity was effectively formed with the CNTs acting as linking bridges between different GNRs. Due to the three-dimensional (3D) conductive network structure of the GNR/CNT hybrid and fine dispersion and alignment inside the PI fibers, as well as the good interfacial interaction between the GNR/CNT hybrid and the PI matrix, PI-GNR/CNT composite films exhibit a unique property of anisotropic electrical conductivity of 8.3 × 10(-2) S cm(-1) in the parallel direction along the fibers and 7.2 × 10(-8) S cm(-1) in the perpendicular direction, which may open the way for wide potential applications of anisotropic conductive nanomaterials in practical production and scientific research fields.

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Three-dimensional carbon nanoparticles (CPs)/Ni-Al layered double hydroxide (NiAl-LDH) (CP/LDH) hybrids with hierarchical nanostructures have been facilely prepared with NiAl -LDH nanosheets homogeneously located on the surface of CPs through an in -situ hydrothermal growth process. Eco-friendly synthesized from the fallen ginkgo leaves, CPs with mesoporous architecture are chemically activated and used as building blocks for the construction of hierarchical CP/LDH hybrids. Mesoporous CPs coupled with the NiAl-LDH nanosheets are favorable to improve the mass transfer, adsorption/desorption of ions, as well as the electrochemical performance of the electrodes. The electrochemical measurements show that CP/LDH hybrid exhibits a remarkably enhanced specific capacitance of 1355 F g -1 at 5 mV s -1 , compared with 121 F g -1 of CPs and 405 F g -1 of pure NiAl-LDHs, as a result of the synergistic effect from electrochemical double layer capacitance of CPs and pseudocapacitance of NiAl-LDHs. Furthermore, the CP/LDH hybrid shows excellent rate capability and good long-term cycling performance with 90% capacitance retained after 2000 cycles. Therefore, the facilely prepared CP/LDH hybrids are promising electrode materials for potential applications in energy storage devices.