Search

Reasonably regulating electronic coupling to promote charge transfer and exciton separation has been regarded a promising approach in catalysis. The material engineering of van der Waals heterojunction (vdWsH) based on two-dimensional (2D) materials would be a potential way to optimize the as-prepared extrinsic physicochemical characteristics. However, it was still an almost uncultivated land waiting for exploration in catalysis. Herein, we introduced the inert h-boron nitride (h-BN) in non-metal reduced graphene oxide (GN) catalysts and constructed BN-GN vdWsH. The theoretical calculation demonstrated that the h-BN can effectively modify the electronic properties of graphene. With the introduction of h-BN, the BN-GN vdWsH can obviously enhance the catalytic activity of Li-CO2 battery. The existence of BN-GN vdWsH can reduce the overpotential more than 700 mV compared with reduced graphene oxide during the CO2 reduction reaction (CO2RR) and CO2 evolution reaction (CO2ER), and it extended cyclic stability more than three times, which was one of the most outstanding non-metallic catalysts. The reasonable structure design made it work as a high efficient electrocatalyst, which shed light on the development for functional treatment of catalytic materials.

Lithium-oxygen batteries have attracted considerable interest in the past a few years, because they have higher theoretical specific energy than Li-ion batteries. However, the available energy densities of the Li-O2 batteries are much less than expected. It is particularly urgent to find catalyst with high activity. Herein, a series of Co3O4 with different morphologies (ordered two-dimensional porous nanosheets, flowerlike and cuboidlike) were successfully prepared through facile hydrothermal and calcination methods. Ordered two-dimensional Co3O4 nanosheets show the best cycling stability. Detailed experimental results reveal that the superiority of the unique two-dimensional uniform porous structures is vital for Li-O2 batteries cathode catalysts. Due to the ordered structures with high surface areas and active sites, the catalysts indicate a high specific discharge capacity of about 10,417 mAh/g at a current density of 200 mA/g, and steadily cycle for more than 50 times with a limited capacity of 1,000 mAh/g.

Magnetic metals (Fe, Co, Ni) and alloys thereof are easily synthesized as nanoparticles, but obtaining highly dispersed graphene-based magnetic nanomaterials remains challenging. Here, three CoNi/graphene nanocomposites (CoNi/GN) are successfully assembled for the first time via a one-pot strategy without templating by manipulating the reaction time and solvents used for the same precursors. Moreover, the reduction of graphene oxide utilizing this method is more effective than that by conventional methods and the alloy particles are firmly embedded on the GN substrate. Compared to n- and p-CoNi/GN nanocomposites, o-CoNi/GN nanocomposites show the best electromagnetic wave absorption properties with the maximum reflection loss of −31.0 dB at 4.9 GHz for a thickness of 4 mm; the effective absorption bandwidth (< 10.0 dB) is 7.3 GHz (9.5–16.8 GHz) for a thickness of 2 mm. The structures and electromagnetic wave absorption mechanisms of the three composites were also investigated. This research provides a new platform for the development of magnetic alloy nanoparticles in the field of microwave-absorbing devices.

Lithium-rich manganese-based layered materials have been considered as the most promising cathode materials for future high-energy-density lithium-ion batteries. However, a great loss of irreversible capacity at the initial cycle, poor cycle stability, and rate performance severely restrict its application. Herein, we develop a new strategy to synthesize hierarchical hollow Li1.2Mn0.54Ni0.13Co0.13O2 microspheres using sucrose and cetyltrimethylammonium bromide as a soft template combined with hydrothermal assisted homogeneous precipitation method. The hollow microspheres are assembled by the primary particles with the size of 50 nm. As a result, the as-prepared material exhibits high reversible capacity, good cycling stability, and excellent rate property. It delivers a high initial discharge capacity of 305.9 mAh g−1 at 28 mA g−1 with coulombic efficiency of 80%. Even at high current density of 560 mA g−1, the sample also shows a stable discharge capacity of 215 mAh g−1. The enhanced electrochemical properties are attributed to the stable hierarchical hollow sphere structure and the appropriate contact area between electrode and electrolyte, thus effectively improve the lithium-ion intercalation and deintercalation kinetics.