Joerg Hermann

We discuss the use of a semi-empirical method to obtain the energy values of 391 energy levels and dipolar-electric radiative transition probabilities in neutral aluminium. A relativistic Hartree–Fock atomic structure code allowing superposition of configurations coupled with a least-square fit procedure has been used for this purpose. Einstein coefficients for spontaneous emission not yet tabulated by the NIST atomic spectra database are reported for several transitions.

The detection of impurities in diatomite is a critical issue during the silicon extraction process.

Elemental analyses of thin films with complex composition are challenging as the standard analytical techniques based on measurement calibration are difficult to apply. We show that calibration-free laser-induced breakdown spectroscopy (LIBS) presents a powerful solution, enabling quantitative analyses of multielemental thin films with analytical performances better than those obtained with other techniques. The demonstration is given for a nickel-chromium-molybdenum alloy film of 150 nm thickness that was produced by pulsed laser deposition. The LIBS spectra were recorded under experimental conditions that enable simple and accurate modeling of plasma emission. Thus, a calibration-free approach based on the calculation of the spectral radiance of a uniform plasma in local thermodynamic equilibrium was applied to deduce the elemental composition. Supported by analyses via Rutherford backscattering spectrometry and energy-dispersive X-ray spectroscopy, the LIBS measurements evidence nonstoichiometric mass transfer of the alloy during the thin-film deposition process. This technique could be used even for thinner films, provided that the film-composing elements are not present in the substrate.

Tritium detection poses a challenge because of the weak beta particle emission and absence of ionizing radiation. We demonstrate the isotopic analysis of deuterated water via laser-induced breakdown spectroscopy as a modality for measuring tritium.

Spatial segregation of species presents one of the main challenges in quantitative spectroscopy of laser-produced plasmas, as it may lead to overestimation of the concentration of the heavier species. Analytical capabilities can also be affected by excessive Stark broadening at atmospheric pressure, hindering the ability to spectrally resolve closely spaced spectral lines, such as those belonging to isotopes of the same element. We present an experimental and modeling study of the segregation of species and spectral line broadening in D₂O-H₂O plasma produced by single- and double-pulse nanosecond laser ablation in air. The ability to resolve Balmer spectral lines of hydrogen and deuterium is investigated by considering the effects of plume segregation. Transient plasma properties which lead to improvements in spectral line separation are discussed. While the plume segregation is found to be negligible in air regardless of the ablation scheme used, we observe a significant improvement in the separation of isotopic spectral lines by employing the double-pulse excitation. This study may lead to increased reliability of optical emission spectroscopy in deuterium-rich plasma environments and suggests the potential for sensitive detection of tritium in air via laser-induced breakdown spectroscopy.