Ultraviolet versus infrared: Effects of ablation laser wavelength on the expansion of laser-induced plasma into one-atmosphere argon gas

Laser-induced plasma from an aluminum target in one-atmosphere argon background has been investigated with ablation using nanosecond ultraviolet (UV: 355 nm) or infrared (IR: 1064 nm) laser pulses. Time- and space-resolved emission spectroscopy was used as a diagnostics tool to have access to the plasma parameters during its propagation into the background, such as optical emission intensity, electron density, and temperature. The specific feature of nanosecond laser ablation is that the pulse duration is significantly longer than the initiation time of the plasma. Laser-supported absorption wave due to post-ablation absorption of the laser radiation by the vapor plume and the shocked background gas plays a dominant role in the propagation and subsequently the behavior of the plasma. We demonstrate that the difference in absorption rate between UV and IR radiations leads to different propagation behaviors of the plasma produced with these radiations. The consequence is that higher electron density and temperature are observed for UV ablation. While for IR ablation, the plasma is found with lower electron density and temperature in a larger and more homogenous axial profile. The difference is also that for UV ablation, the background gas is principally evacuated by the expansion of the vapor plume as predicted by the standard piston model. While for IR ablation, the background gas is effectively mixed to the ejected vapor at least hundreds of nanoseconds after the initiation of the plasma. Our observations suggest a description by laser-supported combustion wave for the propagation of the plasma produced by UV laser, while that by laser-supported detonation wave for the propagation of the plasma produced by IR laser. Finally, practical consequences of specific expansion behavior for UV or IR ablation are discussed in terms of analytical performance promised by corresponding plasmas for application with laser-induced breakdown spectroscopy.