Pulsed laser ablation and plasma chemistry of a carbon–carbon composite in vacuum, air, and oxygen

• Published in: Journal of applied physics 2023-07, Vol.134 (1)
• Main Authors: Radhakrishnan, G., Adams, P. M., Bernstein, L. S.
• Format: Article
• Language: English
• Subjects: Ablation; Absorption spectra; Atmospheric pressure; Carbon; Carbon dioxide; Chemical reactions; Emission spectra; Laser ablation; Lasers; Oxygen; Plasma chemistry; Pulsed lasers; Time measurement
• ISSN: 0021-8979; 1089-7550
• DOI: 10.1063/5.0153331

This work describes the plume chemistry of laser-ablated carbon–carbon (C–C) composite samples in vacuum, a range of air pressures, and in pure oxygen. Time-resolved spectra were measured from a plasma plume generated by laser-ablation at 248 nm. The focus of this work was on the detection of three chemical species, C2, CN, and CO in pressures from near vacuum (10−7 Torr) to air at atmospheric pressure (760 Torr). Emission from atomic carbon C I was predominant at 10−7 Torr, while molecular C2 Swan Band emission was observed at 10−7 Torr, at all air pressures, as well as in pure oxygen. Emission from the CN violet bands was observed only when ablating in air, but not in vacuum or pure O2, indicating that CN was the product of a chemical reaction between an ablated carbon species and N2 present in air, and not intrinsically present in the C–C composite targets. High-resolution emission spectra from C2 and CN were measured and fitted to vibrational and rotational temperatures. Time-resolved emission measurements of both these molecules were used to estimate their respective velocities as a function of pressure. No emission from excited state CO could be detected from 180–900 nm, even in pure O2. However, neutral and ground state CO and CO2 were both detected by measuring FTIR absorption spectra following the ablation of a composite target at 248 nm, in dry air at atmospheric pressure. The HITRAN database was used to calculate the concentrations of CO and CO2 produced per laser pulse.