Influence of the laser pulse duration on spectrochemical analysis of solids by laser-induced plasma spectroscopy.

Quantitative analysis of aluminum and copper alloys by means of laser-induced plasma spectroscopy (LIPS) has been investigated for three representative laser pulse durations (80 fs, 2 ps, and 270 ps). The experiments were carried out in air at atmospheric pressure with a constant energy density of 20 J/cm2. Because the decay rate of the spectral emission depends on the laser pulse duration, the optimum detection requires an optimization of the temporal gating acquisition parameters. LIPS calibration (sensitivity and nonlinearity) and the limit of detection (LOD) are discussed in detail. While the LOD of minor elements embedded in alloy samples obtained by sub-picosecond or sub-nanosecond laser pulses are both time and element dependent, provided an appropriate temporal window is chosen, the optimum LODs (several parts per million (ppm)) prove to be independent of the laser pulse duration. Finally, it is found that for elements such as those detected here, gated LIPS spectra using picosecond or sub-picosecond laser pulses provide much better LOD values than non-gated spectra.

Fluid modeling of the laser ablation depth as a function of the pulse duration for conductors.

Laser ablation of an aluminum target as a function of the pulse duration, for fluences up to 30 J/cm(2) and a wavelength of 0.8 microm, is investigated by means of a fluid code. For a given fluence, the ablation depth shows a minimum for a pulse duration of approximately 10 ps between a maximum obtained for pulses shorter than approximately 1 ps and a lower maximum obtained for pulses in the nanosecond range, in qualitative agreement with published experimental results. The decrease in ablation depth with increase in pulse duration observed between 1 and 10 ps results from the reduced temperature rise near the surface due to increased inward heat transport. The increase in the ablation depth above approximately 10 ps is due to the increase in electron density gradient length while the laser pulse intensity is close to maximum, which thus enables the plasma to absorb more of the laser pulse energy for increased ablation.

Critical-point phase separation in laser ablation of conductors.

Laser ablation due to an ultrashort laser pulse on a massive aluminum target was investigated by means of a one-dimensional fluid code. Clear separation between the ablated matter and the unablated target is seen to occur through spinodal decomposition involving thermodynamic instabilities near the critical point of aluminum. The code also shows that the end of the ablation process is preceded by the ejection of droplets, which form about 15% of the total ejected mass.