Nanosecond laser shock detonation of nanodiamonds:from laser-matter interaction to graphite-to-diamond phase transition

Nanodiamonds(NDs)have been widely explored for applications in drug delivery,optical bioimaging,sensors,quantum computing,and others.Room-temperature nanomanufacturing of NDs in open air using confined laser shock detonation(CLSD)emerges as a novel manufacturing strategy for ND fabrication.However,the fundamental process mechanism remains unclear.This work investigates the underlying mechanisms responsible for nanomanufacturing of NDs during CLSD with a focus on the laser-matter interaction,the role of the confining effect,and the graphite-to-diamond transition.Specifically,a first-principles model is integrated with a molecular dynamics simulation to describe the laser-induced thermo-hydrodynamic phenomena and the graphite-to-diamond phase transition during CLSD.The simulation results elucidate the confining effect in determining the material’s responses to laser irradiation in terms of the temporal and spatial evolutions of temperature,pressure,electron number density,and particle velocity.The integrated model demonstrates the capability of predicting the laser energy threshold for ND synthesis and the efficiency of ND nucleation under varying processing parameters.This research will provide significant insights into CLSD and advance this nanomanufacturing strategy for the fabrication of NDs and other high-temperature-high-pressure synthesized nanomaterials towards extensive applications.

Crossed Beam Study on the F+D2→DF+D Reaction at Hyperthermal Collision Energy of 23.84 kJ/mol

We presented an experimental apparatus combining the H-atom Rydberg tagging time-of-flight technique and the laser detonation source for studying crossed beam reactions at hyperthermal collision energies. The preliminary study of the F+D2→DF+D reaction at hyperthermal collision energy of 23.84 kJ/mol was performed. Two beam sources were used in this study: one is the hyperthermal F beam source produced by a laser detonation process, and the other is D2 beam source generated by liquid-N2 cooled pulsed valve. Vibrational state-resolved di erential cross sections (DCSs) of product for the title reaction were determined. From the product vibrational state-resolved DCS, it can be concluded that products DF(v'=0, 1, 2, 3) are predominantly distributed in the sideway and backward scattering directions at this collision energy. However, the highest vibrational excited product DF(v'=4), is clearly peaked in the forward direction. The probable dynamical origins for these forward scattering products were analyzed and discussed.