Alexander A. Bol'shakov

Laser plasma spectrochemistry

An overview of laser plasma spectrochemistry is presented to demonstrate its wide range of capabilities. Laser plasmas offer the ability to perform elemental, isotopic, molecular, quantitative and qualitative sample analysis with sub-micron spatial resolution, and each feature can be measured at standoff distances. Obviously, these attributes are not all achievable at the same time, but they can be optimized for specific applications. This manuscript gives a sampling (pun intended) of the research in our group that has demonstrated each of these capabilities. Although the technology is commonly referred to as LIBS (laser-induced breakdown spectroscopy), the authors prefer to use laser plasma spectrometry to represent the underlying science.

Laser ablation molecular isotopic spectrometry (LAMIS): current state of the art

Laser Ablation Molecular Isotopic Spectrometry (LAMIS) is a direct and rapid technique that measures optical emission in laser-induced plasmas for isotopic analysis. LAMIS exploits relatively large isotope shifts in spectra of transient molecular isotopologues formed in laser ablation plasma. LAMIS can be performed without sample preparation at atmospheric pressure in open air or inert buffer gases. A spectrometer with modest spectral resolution can be suitable for both LIBS and LAMIS techniques, and thus elemental and isotopic measurements can be accomplished on the same instrument. To date, detection of several isotopes (H, B, C, N, O, Cl, Sr, and Zr) in laser ablation plumes was demonstrated. Precision of quantitative LAMIS measurements was within 9‰ for the 10B/11B ratio determined with confidence of 95% (2σ-interval). Simultaneous determination of isotopes of different elements was shown to be physically possible, while determination of several isotopes of the same element was successfully demonstrated (Sr, Zr). The studies on double-pulse LAMIS and femtosecond LAMIS indicated further prospects for improving accuracy and sensitivity in this technique. A possibility of semi-quantitative isotopic analysis at distances up to 7.8 m without using calibration standards was demonstrated. The latter technique was named as Femtosecond Filament-induced Laser Ablation Molecular Isotopic Spectrometry (F2-LAMIS). Application of LAMIS in industrial, laboratory, and field operations is possible; and such measurements can be realized at a standoff distance to the sample.

Electron temperature and radiative attachment continua in enclosed inductively coupled plasma in argon and chlorine

Inductively coupled plasma (ICP) discharges in chlorine, argon, and their mixtures sustained inside a spherical quartz container at atmospheric pressure have been investigated. Continua of radiative attachment of a free electron to a chlorine atom in ICP are elucidated and are utilized to derive a spatial profile of electron temperature. A qualitative picture of elementary processes in enclosed ICP is given. Differences between electron and gas temperatures are discussed. Electron temperature is maximum in a periphery layer near the induction coil that is chosen for impurity determination. Concentrations of carbon and metal impurities are estimated.

Laser-ablation optical-cavity isotopic spectrometer for Mars rovers

A concept of a compact device for analyzing key isotopic composition in surface materials without sample preparation is presented. This design is based on an advanced modification of Laser Induced Breakdown Spectroscopy (LIBS). First, we developed Laser Ablation Molecular Isotopic Spectrometry (LAMIS) that involves measuring isotope-resolved molecular emission, which exhibits significantly larger isotopic spectral shifts than those in atomic transitions. Second, we used laser ablation to vaporize the sample materials into a plume in which absorption spectra can be measured using a tunable diode laser. The intrinsically high spectral resolution of the diode lasers facilitates measurements of isotopic ratios. The absorption sensitivity can be boosted using cavity enhanced spectroscopy. Temporal behavior of species in a laser ablation plasma from solid samples with various isotopic composition was studied. Detection of key isotopes associated with signs of life (carbon, nitrogen, hydrogen) as well as strontium and boron in laser ablation plume was demonstrated; boron isotopes were quantified. Isotope-resolved spectra of many other molecular species were simulated. The experimental results demonstrate sensitivity to 86Sr, 87Sr, and 88Sr with spectrally resolved measurements for each of them. It is possible to measure strontium isotopes in rocks on Mars for radiogenic age determination. Requirements for spectral resolution of the optical measurement system can be significantly relaxed when the isotopic abundance ratio is determined using chemometric analysis of spectra.

Spectral emission enhancement by an electric pulse for LIBS and LAMIS

Enhancement of the emission intensity by a secondary electric pulse following a laser ablation pulse was investigated in application to the chemical analysis by Laser-Induced Breakdown Spectroscopy (LIBS) and Laser Ablation Molecular Isotopic Spectrometry (LAMIS). A stable reheating pulsed discharge presumably sustained in a diffuse glow regime at atmospheric pressure was demonstrated as a rational approach to increase the sensitivity of the optical emission analysis over the conventional single-pulse laser ablation techniques. The enhancement in the emission intensity was illustrated by several examples of both atomic (Ca, Na) and molecular (OH, AlO, CaF) emission in LIBS and LAMIS, respectively. Especially large emission enhancement was realized for isotopologues 16OH, 18OH and 16OD at the transition A2Σ+ → X2Πi (1–0) with clearly resolved lines of their rotational branches. An increase in rotational temperature from 3370 to 4560 K was measured subsequently to the reheating of plasma by a pulsed electric discharge. Such reheating can be especially useful for the minimally destructive analysis, chemical mapping and depth profiling by LIBS. Enhancement in the emission intensity of CaF can be used for further reduction of the detection limits in fluorine determination. A brief review of the earlier publications on the cross-excitation by an electric pulse after laser ablation is provided and a comparison is made to the similar reheating of the ablation plasma in double-pulse LIBS.

Laser ablation plasmas for diagnostics of structured electronic and optical materials during or after laser processing

Laser induced plasma can be used for rapid optical diagnostics of electronic, optical, electro-optical, electromechanical and other structures. Plasma monitoring and diagnostics can be realized during laser processing in real time by means of measuring optical emission that originates from the pulsed laser-material interaction. In post-process applications, e.g., quality assurance and quality control, surface raster scanning and depth profiling can be realized with high spatial resolution (~10 nm in depth and ~3 μm lateral). Commercial instruments based on laser induced breakdown spectrometry (LIBS) are available for these purposes. Since only a laser beam comes in direct contact with the sample, such diagnostics are sterile and non-disruptive, and can be performed at a distance, e.g. through a window. The technique enables rapid micro-localized chemical analysis without a need for sample preparation, dissolution or evacuation of samples, thus it is particularly beneficial in fabrication of thin films and structures, such as electronic, photovoltaic and electro-optical devices or circuits of devices. Spectrum acquisition from a single laser shot provides detection limits for metal traces of ~10 μg/g, which can be further improved by accumulating signal from multiple laser pulses. LIBS detection limit for Br in polyethylene is 90 μg/g using 50-shot spectral accumulation (halogen detection is a requirement for semiconductor package materials). Three to four orders of magnitude lower detection limits can be obtained with a femtosecond laser ablation - inductively coupled plasma mass spectrometer (LA-ICP-MS), which is also provided on commercial basis. Laser repetition rate is currently up to 20 Hz in LIBS instruments and up to 100 kHz in LA-ICP-MS.