Remote Laser-Induced Breakdown Spectroscopy of Bacterial Growths in Carbonate Rocks in a Mars-like Atmosphere.

Understanding the past habitable environments of Mars increases the requirement to recognize and examine modern analogs and to evaluate the mechanisms that may preserve biosignatures in them. The phenomenon that originates and preserves possible microbial biosignatures in mineral phases is of particular interest in astrobiology. On Earth, the precipitation of carbonate matrices can be mediated by bacteria. Besides microbialites and other sedimentary structures, carbonate formations can be observed in certain karstic caves. The present work is focused on the remote laser-induced breakdown spectroscopy (LIBS) characterization of cyanobacteria, exploring the possibilities for identification and discrimination on carbonate substrates. For this purpose, the extremophile cyanobacterium Chroococcidiopsis sp. (collected from the Nerja Cave, Malaga, Spain) was analyzed under laboratory-simulated martian conditions in terms of chemical composition and gas pressure. LIBS results related to acquired molecular emission features allowed bacterial differentiation from the colonized mineral substrate. In addition, the limits of detection were estimated with a laboratory-grown culture of the cyanobacterium Microcystis aureginosa. Our results reveal LIBS's capability to detect biological traces under simulated martian conditions. Additionally, the time-resolved analysis of the biological samples demonstrates the selection of optimal temporal conditions as a critical parameter for the preferential acquisition of molecular species in organic material.

Ultrafast Laser Excitation Improves LIBS Performance for the Analysis of Optically Trapped Single Nanoparticles Owing to Characteristic Interaction Mechanisms.

Owing to the exceedingly small mass involved, complete elemental characterization of single nanoparticles demands a highly precise control of signal background and noise sources. LIBS has demonstrated remarkable merits for this task, providing a unique tool for the multielemental analysis of particles on the attogram-picogram mass scale. Despite this outstanding sensitivity, the air plasma acting as a heat source for particle dissociation and excitation is a meddling agent, often limiting the acquisition of an accurate sample signature. Although thermal effects associated with ultrashort laser pulses are known to be reduced when compared to the widely used nanosecond pulse duration regime, attempts to improve nanoinspection performance using ultrafast excitation have remained largely unexplored. Herein, picosecond laser pulses are used as a plasma excitation source for the elemental characterization of single nanoparticles isolated within optical traps in air at atmospheric pressure. Results for picosecond excitation of copper particles lead to a mass detection limit of 27 attogram, equivalent to single particles 18 nm in diameter. Temporally and wavelength-resolved plasma imaging reveals unique traits in the mechanism of atomic excitation in the picosecond regime, leading to a deeper understanding of the interactions occurring in single nanoparticle spectroscopy.

Optical Trapping as a Morphologically Selective Tool for In Situ LIBS Elemental Characterization of Single Nanoparticles Generated by Laser Ablation of Bulk Targets in Air.

In the present work, the authors introduce a shape-specific methodology for evaluating the full elemental composition of single micro- and nanoparticles fabricated by laser ablation of bulk targets. For this purpose, bronze samples were directly ablated within an ablation cell, originating dry aerosols consisting of multielemental particles. The in situ generated particles were first optically trapped using air at atmospheric pressure as medium and, then, probed by laser-induced breakdown spectroscopy (LIBS). A key aspect of this technology is the circumvention of possible material losses owing to transference into the inspection instrument while providing the high absolute sensitivity of single-particle LIBS analysis. From the results, we deepen the knowledge in laser-particle interaction, emphasizing fundamental aspects such as matrix effects and polydispersity during laser ablation. The dual role of air as the atomization and excitation source during the laser-particle interaction is discussed on the basis of spectral evidences. Fractionation was one of the main hindrances as it led to particle compositions differing from that of the bulk material. To address possible preferential ablation of some species in the laser-induced plasma, two fluence regimes were used for particle production, 23 and 110 J/cm2. LIBS analysis revealed a relationship between chemical composition of the individual particles and their sizes. At 110 J/cm2, 65% of the dislodged particles were distributed in the range of 100-500 nm, leading to a higher variability of the LIBS spectra among the inspected nanoparticles. In contrast, at 23 J/cm2, around 30% of the aerosolized particles were larger than 1 µm. At this regime, the composition better resembled the bulk material. Therefore, we present a pathway to evaluate how adequate the fabrication parameters are toward yielding particles of a specific morphology while preserving compositional resemblance to the parent bulk sample.

Subfemtogram Simultaneous Elemental Detection in Multicomponent Nanomatrices Using Laser-Induced Plasma Emission Spectroscopy within Atmospheric Pressure Optical Traps.

Simultaneous detection of multiple constituents in the characterization of state-of-the-art nanomaterials is an elusive topic to a majority of the analytical techniques covering the field of nanotechnology. Optical catapulting (OC) and optical trapping (OT) have recently been combined with laser-induced breakdown spectroscopy (LIBS) to provide single-nanoparticle resolution and attogram detection power. In the present work, the multielemental capabilities of this approach are demonstrated by subjecting two different types of nanometric ferrite particles to LIBS analysis. Up to three metallic elements in attogram quantities are consistently detected within single laser events. Individual excitation efficiency for each species is quantified from particle spectra showing an exponential correlation between photon production and the energy of the upper level of the monitored atomic line. Moreover, a new sampling strategy based in skimmer-like 3D printed cones that allows for thin dry nanoparticle aerosols to be formed via optical catapulting is introduced. Enhanced sampling resulted in an increase of the sampling throughput by facilitating stable atmospheric-pressure optical trapping of individual particles and spectroscopic chemical characterization within a short timeframe.

Spectral Identification in the Attogram Regime through Laser-Induced Emission of Single Optically Trapped Nanoparticles in Air.

Current trends in nanoengineering are bringing along new structures of diverse chemical compositions that need to be meticulously defined in order to ensure their correct operation. Few methods can provide the sensitivity required to carry out measurements on individual nano-objects without tedious sample pre-treatment or data analysis. In the present study, we introduce a pathway for the elemental identification of single nanoparticles (NPs) that avoids suspension in liquid media by means of optical trapping and laser-induced plasma spectroscopy. We demonstrate spectroscopic detection and identification of individual 25(±3.7) to 70(±10.5) nm in diameter Cu NPs stably trapped in air featuring masses down to 73±35 attograms. We found an increase in the absolute number of photons produced as size of the particles decreased; pointing towards a more efficient excitation of ensembles of only ca. 7×105 Cu atoms in the onset plasma.

Multi-Pulse Excitation for Underwater Analysis of Copper-Based Alloys Using a Novel Remote Laser-Induced Breakdown Spectroscopy (LIBS) System.

In this work, the use of multi-pulse excitation has been evaluated as an effective solution to mitigate the preferential ablation of the most volatile elements, namely Sn, Pb, and Zn, observed during laser-induced breakdown spectroscopy (LIBS) analysis of copper-based alloys. The novel remote LIBS prototype used in this experiments featured both single-pulse (SP-LIBS) and multi-pulse excitation (MP-LIBS). The remote instrument is capable of performing chemical analysis of submersed materials up to a depth of 50 m. Laser-induced breakdown spectroscopy analysis was performed at air pressure settings simulating the conditions during a real subsea analysis. A set of five certified bronze standards with variable concentration of Cu, As, Sn, Pb, and Zn were used. In SP-LIBS, signal emission is strongly sensitive to ambient pressure. In this case, fractionation effect was observed. Multi-pulse excitation circumvents the effect of pressure over the quantitative analysis, thus avoiding the fractionation phenomena observed in single pulse LIBS. The use of copper as internal standard minimizes matrix effects and discrepancies due to variation in ablated mass.

Elemental analysis of materials in an underwater archeological shipwreck using a novel remote laser-induced breakdown spectroscopy system.

LIBS analysis of submerged materials in an underwater archeological site has been performed for the first time. A fiber-optics-based remote instrument was designed for the recognition and identification of archeological assets in the wreck of the Bucentaure (Bay of Cadiz, South of Spain). The LIBS prototype featured both single-pulse (SP-LIBS) and multi-pulse excitation (MP-LIBS). The use of multi-pulse excitation allowed an increased laser beam energy (up to 95 mJ) transmitted through the optical fiber. This excitation mode results in an improved performance of the equipment in terms of extended range of analysis (to a depth of 50 m) and a broader variety of samples to be analyzed (i.e., rocks, marble, ceramics and concrete). Compared to single-pulse, an intensity enhancement factor of 15× was observed at the same irradiance value, 1.89 GW/cm(2). Thus, a longer pulse duration promotes the heating and melting of the sample, resulting in a greater mass ablated. As a consequence of the optimization of experimental conditions performed in laboratory, underwater characterization of ancient pottery was achieved.

Spatial distribution analysis of strontium in human teeth by laser-induced breakdown spectroscopy: application to diagnosis of seawater drowning.

The diagnosis of drowning can be extremely difficult, especially when the typical morphological signs of drowning are not present, or when the body is in an advanced stage of putrefaction. The main aim of this work is to demonstrate the applicability of laser-induced breakdown spectroscopy (LIBS) to the diagnosis of seawater drowning. Ten teeth samples were selected from eight medico-legal autopsies. A Nd:YAG laser operating at its fundamental wavelength (1,064 nm) was used to generate microplasmas at the sample surface. Strontium (Sr) concentration in tooth samples has been found to be a key factor for the diagnosis of seawater drowning. Spectral differences between the dentin and the enamel were observed. Greater Sr abundance was located in the dentin, with relative standard deviations in the range of 30 to 35%. In addition, chemical images were generated to study the spatial distribution of Sr along the piece. In all cases, Sr content was higher when the cause of the individual death was drowning. A blind experiment was performed to exclude the possibility that the increase of Sr is due to passive diffusion in the blood. The detection of Sr as well as the determination of its distribution by LIBS in dentin seems to be a promising complementary tool for the diagnosis of death by seawater drowning.

Effect of pulse duration in multi-pulse excitation of silicon in laser-induced breakdown spectroscopy (LIBS).

The aim of this study is to investigate the mechanisms responsible for the increase in ablated mass and signal enhancement observed on multi-pulse excitation. Several experiments were designed to obtain evidence that confirms the laser-sample and/or laser-plasma interaction, with special attention to the role of the pulse width on these effects. A train of pulses, with a separation of a few microseconds between pulses, was used for laser-induced breakdown spectroscopy (LIBS) analysis. The signal emission of Si was improved by an enhancement factor of about 60 compared to conventional single-pulse LIBS (SP-LIBS). The number of spikes, their amplitude, and their pulse duration were found to be variable for different Q-switch delays. A temporal study was performed to determine whether or not a laser-plasma interaction took place. The effect of pulse width (as responsible of laser-sample interaction) was also evaluated. The results demonstrate that, although both interactions contribute to the observed effect, the process is predominantly governed by the pulse width.