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Abstract This study examines burst laser-induced pitting (BLIP), an understudied surface modification phenomenon driven by ultrafast laser bursts with sub-picosecond to picosecond inter-pulse delays. Through SEM and AFM analysis, we characterize BLIP as sub-micron pits with polarizationdependent oval shapes, alongside high-fluence melting zones and localized ripple-like structures. Unlike conventional LIPSS, BLIP demonstrates exceptional energy coupling efficiency, evidenced by 10× greater damage areas and a steeper fluence-scaling expansion rate than LIPSS, attributed to transient carrier-mediated processes. Pit density decays exponentially with delay (τ ≈ 6.6-8.9 ps), matching the timescale of self-trapped exciton (STE) relaxation, while spatial statistics reveal a delay-driven transition from field-guided ordering (1-5 ps) to randomized distributions (>10 ps). The resonant-like angular distributions and delay-dependent ellipticity reduction indicate competing mechanisms: optical field enhancement dominates at short delays, while energy dissipation and structure disordering prevail at longer delays. Simulation of nanoplasma excitation reveals near-field optical field enhancements responsible for the ellipticity and ripple-like structures. Beyond their fundamental significance, these BLIP nanostructures offer practical functionalities, including use as anti-reflection coatings and hydrophobic surfaces. These findings establish BLIP as a new paradigm in ultrafast laser-material interactions, where burst parameters selectively activate defect-mediated or field-driven modification pathways in dielectrics. 

Abstract The creation of localized bulk modification using femtosecond pulses inside semiconductors like silicon (Si) is quite challenging, whereas it is not difficult to achieve it for dielectric materials like fused silica (FS). This report addresses the fundamental origin of this issue. By taking a simple numerical approach, it has been found that in FS we can deliver stronger fluence due to self-focusing at higher power levels compared to Si. The origin for the above lies in the spatio-temporal pulse-splitting behavior, which is dominant in the case of FS at the focus, whereas, for Si, it is only effective after focus. We have also considered the influence of plasma and Kerr terms to elucidate the reason behind these nonlinearities. For the FS case, omission of Kerr term dominates, whereas, for Si, the influence of each term does not significantly create self-focusing like FS under a similar focusing condition. This study could provide an important guideline for researchers to understand the complexity of laser-matter interaction in transparent materials specifically being studied by many laser-processing industries. 

The nature of structural changes of nanosecond laser modification inside silicon is investigated. Raman spectroscopy and transmission electron microscopy measurements of cross sections of the modified channels reveal highly localized crystal deformation. Raman spectroscopy measurements prove the existence of amorphous silicon inside nanosecond laser induced modifications, and the percentage of amorphous silicon is calculated based on the Raman spectrum. For the first time, the high-resolution transmission electron microscopy images directly show the appearance of amorphous silicon inside nanosecond laser induced modifications, which corroborates the indirect measurements from Raman spectroscopy. The laser modified channel consists of a small amount of amorphous silicon embedded in a disturbed crystal structure accompanied by strain. This finding may explain the origin of the positive refractive index change associated with the written channels that may serve as optical waveguides. 

A mathematical model is derived to predict the maximum speed of a focused laser beam in the laser cutting of thin materials. This model contains only two material parameters and is used to obtain an explicit relationship between the cutting speed and laser parameters. The model shows that there exists an optimal focal spot radius with which cutting speed is maximized for a given laser power. We compare the modeling results with experiments and find a good agreement after correcting laser fluence. This work is useful for the practical application of lasers in processing thin materials such as sheets and panels. 

Helical structures exhibit novel optical and mechanical properties and are commonly used in different fields such as metamaterials and microfluidics. A few methods exist for fabricating helical microstructures, but none of them has the throughput or flexibility required for patterning a large surface area with tunable pitch. In this paper, we report a method for fabricating helical structures with adjustable forms over large areas based on multiphoton polymerization (MPP) using single-exposure, three dimensionally structured, self-accelerating, axially tunable light fields. The light fields are generated as a superposition of high-order Bessel modes and have a closed-form expression relating the design of the phase mask to the rotation rate of the beam. The method is used to fabricate helices with different pitches and handedness in the material SU-8. Compared to point-by-point scanning, the method reported here can be used to reduce fabrication time by two orders of magnitude, paving the way for adopting MPP in many industrial applications. 

Bursts of 16 femtosecond laser pulses are generated in a fourfold Michelson interferometer with a tunable delay and envelope. Solutions are given to solve the “forward problem” (bursts from a given parameter set) and “inverse problem” (obtain parameter set from a given burst). Three types of bursts are generated experimentally with envelopes suitable for applications in laser materials processing and the generation of terahertz radiation.