We report physical processes responsible for the periodic nanostructure formation in femtosecond-laser ablation of thin film surfaces. It has been found that an initial random distribution of nanoscale ablation traces is periodically structured with an increase in superimposed laser pulses or fluence on diamond-like carbon film used as the target. The results show that the formation of periodicity can be attributed to the excitation of surface plasmon polaritons to induce the periodic enhancement of local fields in the surface layer. The estimated field period is in good agreement with the observed size of nanostructures.

We investigated an Laguerre-Gaussian (LG) beam that can carry an orbital angular momentum and has a doughnut-shaped intensity pattern. We developed a multilevel spiral phase plate (SPP) that generates an LG beam by applying the wave surface of a spiral structure directly to a Gaussian beam for application to microscopic laser material processing.We experimentally demonstrate, for the first time, that it is possible to generate an LG beam with the multilevel SPP that allows the use in high intensity laser pulses.

Focused on silicon surface in water, superimposed multiple shots of linearly polarized 800-nm, 100-fs, 10-Hz laser pulses at lower fluence than the single-pulse ablation threshold are shown to produce two kinds of periodic nanostructures with almost constant periods of 150 nm and 400 nm. Surface plasmon polaritons excited in the surface layer illustrates well the formation of nanostructures and its dynamic properties observed. Pump and probe measurements of the ultrafast change in surface reflectivity during the interaction have demonstrated that the multiple low-fluence fs pulses are crucial to the nanostructuring through the accumulation of non-thermal bonding structure change and the subsequent nanoscale ablation.

High-order harmonic generation is demonstrated to provide a sensitive way for an extensive study of dynamic processes in the field-free alignment of strong-field-induced molecular rotational wave packets. The time-dependent harmonic signal observed from field-free-aligned N2, O2, and CO2 has been found to include two sets of beat frequency for pairs of coherently populated rotational states. One of them is the well-known frequency component characterizing the field-free alignment of molecules, and the other is ascribed to the beat that arises from coherence embedded in the wave packet. We discuss the effect of each frequency component on the revival signal observed with the harmonic generation.

Structure of diamondlike carbon films deposited by femtosecond and nanosecond pulsed laser ablation