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In this paper, the new approach for Laser Induced Breakdown Spectroscopy (LIBS) based on nanoparticle deposition on the sample surface is reviewed from both fundamental and application points of view. The case of Nanoparticle-Enhanced LIBS (NELIBS) of metal samples is used for describing and discussing the main causes of the emission signal enhancement. A set of test cases is presented, which shows enhancements up to 1–2 orders of magnitude obtained using NELIBS with respect to LIBS. The feasibility and potential of NELIBS are also discussed for several analytical applications, including analysis of metallic samples, transparent samples and aqueous solutions. [ABSTRACT FROM AUTHOR]

In the last decade Pulsed Laser Ablation in Liquids (PLAL) has been widely investigated from the fundamental point of view, and various theories have been proposed. Although many important achievements have been obtained by the scientific community, many aspects still need to be clarified and many contradictions arise when comparing the interpretation of similar experiments carried out by different authors. In this paper we have reconsidered previous works focused on specific processes and stages of the PLAL, in order to outline a modern and comprehensive point of view of the overall physical aspects of PLAL. With this aim, several simultaneous diagnostic methods have been applied during the production of metallic nanoparticles (NPs), i.e. optical emission spectroscopy and fast imaging for the investigation of the laser-induced plasma, shadowgraph for the study of the cavitation bubble, and Double Pulse Laser Ablation in Liquid (DP-LAL) and laser scattering for the investigation of NPs location and mechanisms of release in solution. The connection between the various stages of the DP-LAL allows understanding the main characteristics of the produced NPs and the typical timescales of the basic mechanisms involved in PLAL. [ABSTRACT FROM AUTHOR]

In this article, an increase of 1-2 orders of magnitude in laser-induced breakdown spectroscopy (LIBS) signals was obtained by depositing silver nanoparticles on metal samples. Nanoparticle-enhanced LIBS (NELIBS) was found to be a robust and flexible tool for the chemical analysis of metals because the sample emission signal did not appear to be affected much by the size and concentration of deposited nanoparticles (NPs) within the ranges of 10 nm for diameter and 1 order of magnitude for concentration. On the other hand, preliminary NELIBS tests on insulators and semiconductors did not show any significant enhancement with respect to conventional LIBS. In this article, we present a detailed investigation of the fundamental features of NELIBS spectra, in addition to some examples of analytical applications to the quantitative analysis of metal alloys. [ABSTRACT FROM AUTHOR]

Abstract: A self-calibrated analytical technique, based on plasmas induced by either 250fs or 7ns laser pulses, is presented. This approach is comparable to other calibration-free methods based on LTE assumption. In order to apply this method to very different laser pulse durations, the partial-local thermodynamic equilibrium (p-LTE) has been considered within the energy range of 30,000–50,000cm−1. In order to obtain the neutral species densities, the detected plasma species emission lines intensities have been treated together with the experimental evaluated background black-body Planck-like emission distribution. For validating the followed method, three certified copper-based-alloys standards were employed and their minor components (Ni, Pb and Sn) amounts were determined. As a result, it arises, that this standardless method, independently from the laser source pulse durations, provides good quantitative analysis, and, consequently, that the composition of the plasma plume emitting species induced is not affected by the laser pulse time width. [Copyright &y& Elsevier]

Real-time analysis of fine ash in volcanic plumes, which represent magma fragments expelled from the crater during explosive eruptions, is a valuable tool for volcano monitoring and hazard assessment. To obtain the chemical characterization of the juvenile pyroclastic material emitted in volcanic plumes, many analytical techniques can be used. Among them, laser-induced breakdown spectroscopy (LIBS) is the one that can most easily be adapted to advanced applications in extreme environments. In this paper, LIBS experiments based on self-calibrated approaches are used to determine the elemental composition of suspended volcanic ash. To simulate the conditions of dispersed volcanic ash in the atmosphere, different sizes of volcanic ash samples are suspended in the air by laser-induced shockwaves in a dedicated chamber, and a parametric study is carried out to establish the optimal experimental conditions for recording usable plasma emission spectra for each ash size. The quantitative analysis is performed using a self-calibrated analytical method, including calibration-free LIBS, which is based on the calculation of the spectral radiance of a uniform plasma in local thermodynamic equilibrium. The method accounts intrinsically for self-absorption since it modifies the intensity of spectral lines and thus leads to an underestimation of the elemental fraction. An intensity calibration of the spectra based on the measurements of Fe lines intensities was also used in this work to deduce the apparatus response from the spectrum itself and avoid the use of standard calibration lamps. Results demonstrate the potential of real-time measurements of elemental fractions in volcanic ash with good agreement with the literature composition., Competing Interests: Declaration of Conflicting InterestsThe authors declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Nanoparticle-enhanced laser-induced breakdown spectroscopy (NELIBS) is an optical emission technique based on the laser-induced plasma (LIP) on a sample after the deposition of plasmonic nanoparticles (NPs) on its surface. The employment of the NPs allows an enhancement of the signal with respect to the one obtained with the conventional laser-induced breakdown spectroscopy (LIBS) enabling an extremely high sensitivity and very low limits of detection compared with the LIBS performance. Recently, NELIBS was used for monitoring the NP protein corona formation. As a matter of fact, the NPs in the presence of proteins adsorbed on the surface change their surface properties, therefore the sensing of protein corona formation was possible because of the strong dependence of NELIBS effects on the NP organization on the substrate, which in turn is deeply affected by the surface properties of the NPs. A correlation was found between NELIBS enhancement and the structure of the NP-protein conjugate in terms of protein content absorbed on the NP surface. An interesting question that was not yet exploited regards the role of LIP during the NELIBS when the NPs are covered with proteins. Since the presence of organic matter can strongly quench the LIP emission, the study of the LIP properties during protein corona sensing by NELIBS is of interest for two main reasons: (i) to understand whether the plasma parameters can vary in the presence of proteins adsorbed on the NP surface and (ii) to investigate how and if the plasma parameters themselves can influence the NELIBS processes. With this aim, the study of plasma parameters, i.e., electron densities and temperatures, during the sensing of NP protein corona by NELIBS is presented and discussed. The NPs used during these experiments were ultrapure gold NPs (AuNPs) produced by pulsed laser ablation in liquid, which are stable without any stabilizer. The human serum albumin protein is used to form AuNP-protein conjugates further deposited on a titanium target in NELIBS measurements. Dynamic light scattering, surface plasmon resonance spectroscopy, and laser Doppler electrophoresis for ζ-potential determination were employed to monitor the protein coverage of NP surface in the conjugate solutions before the NELIBS measurements., Competing Interests: Declaration of Conflicting InterestsThe authors declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Gulf War illness (GWI) is a chronic illness with no known validated biomarkers that affects the lives of hundreds of thousands of people. As a result, there is an urgent need for the development of an untargeted and unbiased method to distinguish GWI patients from non-GWI patients. We report on the application of laser-induced breakdown spectroscopy (LIBS) to distinguish blood plasma samples from a group of subjects with GWI and from subjects with chronic low back pain as controls. We initially obtained LIBS data from blood plasma samples of four GWI patients and four non-GWI patients. We used an analytical method based on taking the difference between a mean LIBS spectrum obtained with those of GWI patients from the mean LIBS spectrum of those of the control group, to generate a "difference" spectrum for our classification model. This model was cross-validated using different numbers of differential LIBS emission peaks. A subset of 17 of the 82 atomic and ionic transitions that provided 70% of correct diagnosis was selected test in a blinded fashion using 10 additional samples and was found to yield 90% classification accuracy, 100% sensitivity, and 83.3% specificity. Of the 17 atomic and ionic transitions, eight could be assigned unambiguously to species of Na, K, and Fe.

Alzheimer's disease (AD) is a progressive incurable neurodegenerative disease and a major health problem in aging population. We show that the combined use of Laser-Induced Breakdown Spectroscopy (LIBS) and machine learning applied for the analysis of micro-drops of plasma samples of AD and healthy controls (HC) yields robust classification. Following the acquisition of LIBS spectra of 67 plasma samples from a cohort of 31 AD patients and 36 healthy controls (HC), we successfully diagnose late-onset AD (> 65 years old), with a total classification accuracy of 80%, a specificity of 75% and a sensitivity of 85%., Competing Interests: Declaration of Competing Interest The authors declare no conflicts of interest. The views expressed in this article are those of the authors and do not represent the views of the US Department of Veterans Affairs or the US Government.

In this paper, nanoparticle enhanced laser-induced breakdown spectroscopy (NELIBS) was applied to the elemental chemical analysis of microdrops of solutions with analyte concentration at subppm level. The effect on laser ablation of the strong local enhancement of the electromagnetic field allows enhancing the optical emission signal up to more than 1 order of magnitude, enabling LIBS to quantify ppb concentration and notably decreasing the limit of detection (LOD) of the technique. At optimized conditions, it was demonstrated that NELIBS can reach an absolute LOD of few picograms for Pb and 0.2 pg for Ag. The effect of field enhancement in NELIBS was tested on biological solutions such as protein solutions and human serum, in order to improve the sensitivity of LIBS with samples where the formation and excitation of the plasma are not as efficient as with metals. Even in these difficult cases, a significant improvement with respect to conventional LIBS was observed.

Experiments of collinear Double Pulse Laser Ablation in Liquid (DP-LAL) were carried out for studying the production mechanisms of nanoparticles (NPs) in water, which revealed the fundamental role of the cavitation bubble dynamics in the formation of aqueous colloidal dispersions. In this work, DP-LAL was used to generate silver nanoparticles (AgNPs) from a silver target submerged in water at atmospheric pressure and room temperature, by using the second harmonic (532 nm) of two Nd:YAG lasers. The second laser pulse was shot at different delay times (i.e. interpulse delay) during the bubble temporal evolution of the first laser induced bubble. Optical Emission Spectroscopy, Shadowgraph Images, Surface Plasmon Resonance absorption spectroscopy and Dynamic Light Scattering were carried out to study the behaviour of laser-induced plasma and cavitation bubbles during the laser ablation in liquid, to monitor the generation of AgNPs under different conditions, and for characterization of NPs. The results of DP-LAL were always compared with the corresponding ones obtained with Single Pulse Laser Ablation in Liquid (SP-LAL), so as to highlight the peculiarities of the two different techniques.

Although the first nanoseconds to microseconds rule the resulting process yield of laser ablation in liquid, a comprehensive view involving combination of time-resolved measurement techniques is still lacking. In this paper, fundamental aspects of laser ablation of metals in water during the production of nanoparticles are discussed. Three fast diagnostic methods have been applied simultaneously. These are Optical Emission Spectroscopy for the plasma characterization, fast shadowgraph for plasma and cavitation bubble dynamics and laser scattering for the mechanisms of delivery of the produced materials in the liquid. Moreover, in order to validate the discussion, the effect on cavitation dynamics of the ablation of bulk and wire-shaped targets has been investigated together with the relative nanoparticles production yield. Unusual arrow-bow ejection phenomena between the cavitation bubble and the wire result in suppressed material back-deposition, causing efficient ejection of ablated matter into the liquid. The presented nanosecond and microsecond-resolved analysis allows estimating the timescale and role of the basic mechanisms involved in laser ablation in liquids as well as the thermodynamic characteristics of the processes.

Laser Induced Breakdown Spectroscopy (LIBS) is a fast and multi-elemental analytical technique particularly suitable for the qualitative and quantitative analysis of heavy metals in solid samples, including environmental ones. Although LIBS is often recognised in the literature as a well-established analytical technique, results about quantitative analysis of elements in chemically complex matrices such as soils are quite contrasting. In this work, soil samples of various origins have been analyzed by LIBS and data compared to those obtained by Inductively Coupled Plasma-Optical Emission Spectroscopy (ICP-OES). The emission intensities of one selected line for each of the five analytes (i.e., Cr, Cu, Pb, V, and Zn) were normalized to the background signal, and plotted as a function of the concentration values previously determined by ICP-OES. Data showed a good linearity for all calibration lines drawn, and the correlation between ICP-OES and LIBS was confirmed by the satisfactory agreement obtained between the corresponding values. Consequently, LIBS method can be used at least for metal monitoring in soils. In this respect, a simple method for the estimation of the soil pollution degree by heavy metals, based on the determination of an anthropogenic index, was proposed and determined for Cr and Zn.

Analytical applications of Laser Induced Breakdown Spectroscopy (LIBS), namely optical emission spectroscopy of laser-induced plasmas, have been constantly growing thanks to its intrinsic conceptual simplicity and versatility. Qualitative and quantitative analysis can be performed by LIBS both by drawing calibration lines and by using calibration-free methods and some of its features, so as fast multi-elemental response, micro-destructiveness, instrumentation portability, have rendered it particularly suitable for analytical applications in the field of environmental science, space exploration and cultural heritage. This review reports and discusses LIBS achievements in these areas and results obtained for soils and aqueous samples, meteorites and terrestrial samples simulating extraterrestrial planets, and cultural heritage samples, including buildings and objects of various kinds.