The interaction of ultrashort pulsed laser radiation with intensities of 1013 W cm−2 and above with materials often results in an unexpected high X-ray photon flux. It has been shown so far, on the one hand, that X-ray photon emissions increase proportionally with higher laser power and the accumulated X-ray dose rates can cause serious health risks for the laser operators. On the other hand, there is clear evidence that little variations of the operational conditions can considerably affect the spectral X-ray photon flux and X-ray emissions dose. In order to enhance the knowledge in this field, four ultrashort pulse laser systems for providing different complementary beam characteristics were employed in this study on laser-induced X-ray emissions, including peak intensities between 8 × 1012 W∙cm−2 < I0 < 5.2 × 1016 W∙cm−2, up to 72.2 W average laser power as well as burst/bi-burst processing mode. By the example of AISI 304 stainless steel, it was verified that X-ray emission dose rates as high as > 45 mSv h−1 can be produced when low-intensity ultrashort pulses irradiate at a small 1 µm intra-line pulse distance during laser beam scanning and megahertz pulse repetition frequencies. For burst and bi-burst pulses, the second intra-burst pulse was found to significantly enhance the X-ray emission potentially induced by laser pulse and plasma interaction.
We report on photoionization of ultracold magnetically trapped Rb atoms on an atom chip. The atoms are trapped at in a strongly anisotropic trap. Through a hole in the chip with a diameter of , two laser beams are focused onto a fraction of the atomic cloud. A first laser beam with a wavelength of excites the atoms via a two-photon transition to the level. With a fiber laser at the excited atoms are photoionized. Ionization leads to depletion of the atomic density distribution observed by absorption imaging. The resonant ionization spectrum is reported. The setup used in this experiment is suitable not only to investigate mixtures of Bose-Einstein condensates and ions but also for single-atom detection on an atom chip.
We report on novel observations of directed re-deposition of ablation debris during the ultrafast laser micro-structuring of stainless steel in the air with multi-beams in close proximity on the surface. This interesting phenomenon is observed with both 10 ps and 600 fs NIR laser pulses at 5 kHz repetition rate. Ablation spot geometries could be altered with the use of beam splitting optics or a phase-only Spatial Light modulator. At low fluence (F ~ 1.0 J cm−2) and pulse exposure of a few hundred pulses, the debris appears as concentrated narrow “filaments” connecting the ablation spots, while at higher fluence, (F ~ 5.0 J cm−2) energetic jets of material emanated symmetrically along the axes of symmetry, depositing debris well beyond the typical re-deposition radius with a single spot. Patterns of backward re-deposition of debris to the surface are likely connected with the colliding shock waves and plasma plumes with the ambient air causing stagnation when the spots are in close proximity. The 2D surface debris patterns are indicative of the complex 3D interactions involved over wide timescales during ablation from picoseconds to microseconds.
The ongoing trend in the development of powerful ultrashort pulse lasers has attracted increasing attention for this technology to be applied in large-scale surface engineering and modern microfabrication. However, the emission of undesired X-ray photon radiation was recently reported even for industrially relevant laser irradiation regimes, causing serious health risks for laser operators. In the meantime, more than twenty influencing factors have been identified with substantial effects on X-ray photon emission released by ultrashort pulse laser processes. The presented study on enhanced X-ray emission arising from high pulse repetition frequency ultrashort pulse laser processing provides new insights into the interrelation of the highest-contributing parameters. It is verified by the example of AISI 304 substrates that X-ray photon emission can considerably exceed the legal dose rate limit when ultrashort laser pulses with peak intensities below 1 × 1013 W/cm² irradiate at a 0.5 MHz pulse repetition frequency. The peak intensity threshold value for X-ray emissions decreases with larger laser spot sizes and longer pulse durations. Another key finding of this study is that the suction flow conditions in the laser processing area can affect the released X-ray emission dose rate. The presented results support the development of effective X-ray protection strategies for safe and risk-free ultrashort pulse laser operation in industrial and academic research applications.
A pump–probe setup including a Robert-cell-type delay stage is calculated and built in the presented study. The goal is to visualize laser beam material interactions upon highly repetitive ultrashort pulse irradiations by shadowgraph imaging, which makes a valuable contribution to clarify the occurring interaction phenomena in this field. Ultrashort laser pulses ( ; ) are irradiated onto a bright-rolled stainless steel metal plate (AISI 316). The high-speed shadowgraph sequences are captured for the time-resolved imaging of plasma and shockwave evolution during material ablation. The captured time frame ranges from the time just before the next pulse irradiates the interaction zone until 2 µs after pulse irradiation. The first part of the experimental study features the shockwave dynamics and evolution of the laser plasma/ablation plume as induced upon single-pulse irradiations. It is shown that the expansion velocity of the shockwave decreases from 10 km/s shortly after pulse irradiation to 6.1 km/s at 41 ns after pulse irradiation. The second part deals with laser pulse trains by irradiating up to 10 pulses at 500 kHz pulse repetition frequency to the substrate. For increasing pulse numbers, the shadowgraphs show a steady increase in height and width of the laser plasma/ablation plume that were measured at 2.4 mm in height and 1.2 mm in width after the 10th pulse.