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It has been a long-standing challenge to produce air-stable few-layer black phosphorus (BP) because BP degrade rapidly in ambient atmosphere. Here we demonstrate that the pristine BP with ten layers or more possesses a strong stability and can be stored in air for two weeks. The physical mechanism can be ascribed to the native phosphorus oxide formed on the surface, which act as a stable and protective capping layer and prevent the underlying layer from further oxidation. The pristine 10-layer BP FET device can maintain a high mobility value of around 220 cm2 V-1s−1 in air for 2 weeks. By contrast, the plasma-induced phosphorus oxide is not dense or robust enough to protect the underlying sample from oxidation. These results suggest that the density of the oxide layer on the surface plays a vital role in the stability of BP flakes. This work offers new perspectives for probing the stability of BP based electronic and optoelectronic devices.

Recent years have witnessed successful applications of non-thermal plasmas (NTPs) as efficient and flexible tools for direct conversion of liquid alcohols into higher-value energy carriers at mild or even near-room-temperature conditions. Better understanding of the fundamental physical properties of the liquid alcohol discharges is needed for development and optimization of NTP-based applications. Here we investigate the discharge characteristics of a plasma-based liquid ethanol conversion under different process parameters and reveal the general trends of the discharge behavior. Two discharge modes, namely the self-pulsed and direct current (DC) modes, are sustained during the in-liquid discharge. These two modes can be easily interchanged and flexibly controlled by adjusting the processing parameters. The behavior of the bubbles generated during the discharge plays an important role in the transition between the discharge modes. When the discharge is sustained with the diffusion and floating of the bubbles, the DC mode is observed. Otherwise, the discharge develops into the pulse mode. The production rates and composition of the gaseous products are also shown to depend on the discharge modes.

Highly size-controllable synthesis of free-standing perfectly crystalline silicon carbide nanocrystals has been achieved for the first time through a plasma-based bottom-up process. This low-cost, scalable, ligand-free atmospheric pressure technique allows fabrication of ultra-small (down to 1.5 nm) nanocrystals with very low level of surface contamination, leading to fundamental insights into optical properties of the nanocrystals. This is also confirmed by their exceptional photoluminescence emission yield enhanced by more than 5 times by reducing the nanocrystals sizes in the range of 1-5 nm, which is attributed to quantum confinement in ultra-small nanocrystals. This method is potentially scalable and readily extendable to a wide range of other classes of materials. Moreover, this ligand-free process can produce colloidal nanocrystals by direct deposition into liquid, onto biological materials or onto the substrate of choice to form nanocrystal films. Our simple but efficient approach based on non-equilibrium plasma environment is a response to the need of most efficient bottom-up processes in nanosynthesis and nanotechnology., Funding Agencies|Royal Society International Exchange Scheme [IE120884]; Leverhulme International Network [IN-2012-136]; EPSRC [EP/K022237/1, EP/M024938/1]; EU-FP7 [606889]; University of Ulster Vice-Chancellor Studentship; EU [606889]; CSIRO; Australian Research Council; School of Chemistry, Physics and Mechanical Engineering, Science and Engineering Faculty, Queensland University of Technology