Here, we report the presence of ferromagnetism in hybrid nickel–boron nitride nanotubes (BNNTs) with an ordered structure, synthesized by chemical vapor deposition using elemental boron, nickel oxide as the catalyst, and ammonia gas as the source for nitrogen. In previous studies, the nanotubes were synthesized with two metal oxide catalysts, whereas here, only a single catalyst was used. The nanotube’s structure was determined by X-ray diffraction, scanning electron microscopy, and high-resolution transmission electron microscopy. Purity of the nanotubes synthesized at 1150 °C was exceptional and this was determined by Raman spectroscopy. The average diameter of the nanotubes was 63 nm. Based on the magnetic studies carried out, it can be confirmed that the synthesized hybrid material is ferromagnetic at room temperature. Cyclic voltammetry was carried out to confirm the dielectric nature of the nanotubes. These materials could pave ways to nanoscale devices. The well-known thermal stability of BNNTs would play a vital role in preventing thermal failures in such small-scale devices where overheating is a major concern. The presence of semiconducting and magnetic properties in a single material could be confirmed, which might be highly significant in the field of spintronics.

Doping of heteroatom into well-structured mesoporous carbon architecture can significantly augment the capacitive performance. In this work, we report P-doped graphitic hollow carbon spheres (P-GHCS) grown over Fe-KIT-6 through the in situ approach using the catalytic CVD technique. The obtained P-GHCS possesses a relatively high surface area with uniform mesoporous structure, good graphitization with tunable P-doping contents. The highly favorable structure and desirable heteroatom doping were taken into account to evaluate the P-GHCS as a modified electrode material towards high-performance supercapacitor. The optimized P-GHCS-800 sample exhibits superior specific capacitance (Csp) 321 F g−1 at 0.2 A g−1 with outstanding cycling stability with 2.9% loss of its initial capacitance after 2000 cycles in 6 M KOH electrolyte background in the three-electrode computerized system. More importantly, the fabricated P-GHCS-800 symmetric supercapacitor device can withstand at a wide potential width of 2.0 V, together with remarkable cyclic stability (89.09%) after 2000 cycles at a current density of 1 A g−1 in aqueous 1 M Na2SO4 as electrolyte providing a relatively high energy density of 10.83 Wh kg−1 with a power density of 222.78 W kg−1. Additionally, we demonstrated the single symmetric supercapacitor cell which provided sufficient energy to turn on a red LED of 20 mW and emit light over a certain period of time opens up possible realistic applications.

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