Laser-induced breakdown spectroscopy at a water/gas interface: A study of bath gas-dependent molecular species

Abstract

Single-pulse laser-induced breakdown spectroscopy has been performed on the surface of a bulk water sample in an air, argon, and nitrogen gas environment to investigate emissions from hydrogen-containing molecules. A microplasma was formed at the gas/liquid interface by focusing a Nd:YAG laser beam operating at 1064 nm onto the surface of an ultra-pure water sample. A broadband Echelle spectrometer with a time-gated intensified charge-coupled device was used to analyze the plasma at various delay times (1.0–40.0 μs) and for incident laser pulse energies ranging from 20–200 mJ. In this configuration, the dominant atomic spectral features at short delay times are the hydrogen H-alpha and H-beta emission lines at 656 and 486 nm, respectively, as well as emissions from atomic oxygen liberated from the water and air and nitrogen emission lines from the air bath gas. For delay times exceeding approximately 8 μs the emission from molecular species (particularly OH and NH) created after the ablation process dominates the spectrum. Molecular emissions are found to be much less sensitive to variations in pulse energy and exhibit a temporal decay an order of magnitude slower than the atomic emission. The dependence of both atomic hydrogen and OH emission on the bath gas above the surface of the water was studied by performing the experiment at standard pressure in an atmospheric purge box. Electron densities calculated from the Stark broadening of the H-beta and H-gamma lines and plasma excitation temperatures calculated from the ratio of H-beta to H-gamma emission were measured for ablation in the three bath gases.