Search Results (33)

The development of reproducible and stable plasmon-free substrates for surface-enhanced Raman scattering (SERS) is critical for practical applications in analytical chemistry. Transition metal dichalcogenides (TMDCs) have emerged as promising candidates due to their unique electronic properties, yet their performance is often constrained by the chemical inertness of their pristine basal planes. This work presents a systematic comparison of crystalline flakes and nanoparticles of tungsten diselenide (WSe₂) and tungsten ditelluride (WTe₂), prepared via liquid-phase ultrasonic exfoliation and non-equilibrium femtosecond pulsed laser ablation in liquid (PLAL), respectively. The results demonstrate that nanoparticle-based substrates consistently outperform their flake-based counterparts, achieving enhancement factors in the range of ${10}^4$. The superior performance of the nanoparticles is hypothesized to originate from the synthesis-induced defects and high-curvature regions in the nanoparticles shell which facilitates efficient, defect-mediated charge transfer between the substrate and the analyte. At the same time, the inner polycrystalline volume conserves the important characteristics of the bulk counterparts like excitons in semiconducting WSe₂ and broadband absorption in semimetallic WTe₂, which unblocks the tunable photothermal colloidal response. The study establishes morphology engineering through non-equilibrium synthesis as a powerful and generalizable strategy for designing high-performance, dual-function colloidal platforms, offering a pathway toward robust and reproducible analytical systems. Full article

Sensing represents one of the most rapidly developing areas of modern life sciences, spreading from the detection of pathogenic microorganisms in living systems, food, and beverages to hazardous substances in liquid and gaseous environments. However, the development of efficient and low-cost multimodal sensors with easy-to-read functionality is still very challenging. In this paper, stable aqueous colloidal suspensions (ζ-potential was between −30 and −40 mV) of ultrasmall (~7 nm) plasmonic Si-Au and SiC-Au nanocomposites were formed. Two variants of pulsed laser ablation in liquids (PLAL)—direct ablation and laser co-fragmentation—were used for this purpose. The co-fragmentation approach led to a considerable decrease in hydrodynamic diameter (~78 nm) and bandgap widening to approximately 1.6 eV. All plasmonic nanocomposites exhibited efficient multi-band blue emission peaking at ~430 nm upon Xe lamp excitation. Co-fragmentation route considerably (~1 order of magnitude) increased the PL efficiency of the nanocomposites in comparison with the laser-ablated ones, accompanied by a negligible amount of dangling bonds. These silicon-based nanostructures significantly affected the optical response of rhodamine 6G, depending on the synthesis route. In particular, directly ablated nanoparticles revealed a stronger influence on the optical response of dye molecules. The observed findings suggest using such types of semiconductor-plasmonic nanocomposites for multimodal plasmonic and colorimetric sensing integrated with luminescent detection capability. Full article

Pulsed liquid-based nanoparticle synthesis has emerged as a versatile and environmentally friendly approach for producing a wide range of nanomaterials with tunable properties. Unlike conventional chemical methods, pulsed techniques—such as pulsed laser ablation in liquids (PLAL), electrical discharge, and other energy-pulsing methods—enable the synthesis of high-purity nanoparticles without the need for toxic precursors or stabilizing agents. This review provides a comprehensive overview of the fundamental mechanisms driving nanoparticle formation under pulsed conditions, including plasma–liquid interactions, cavitation, and shockwave dynamics. We discuss the influence of key synthesis parameters, explore different pulsed energy sources, and highlight the resulting effects on nanoparticle size, shape, and composition. The review also surveys a broad spectrum of material systems and outlines advanced characterization techniques for analyzing synthesized nanostructures. Furthermore, we examine current and emerging applications in biomedicine, catalysis, sensing, energy, and environmental remediation. Finally, we address critical challenges such as scalability, reproducibility, and mechanistic complexity, and propose future directions for advancing the field through hybrid synthesis strategies, real-time diagnostics, and machine learning integration. By bridging mechanistic insights with practical applications, this review aims to guide researchers toward more controlled, sustainable, and innovative nanoparticle synthesis approaches. Full article

Achieving targeted nanoparticle (NP) size and concentration combinations in Pulsed Laser Ablation in Liquid (PLAL) remains a challenge due to the highly nonlinear relationships between laser processing parameters and NP properties. Despite the promise of PLAL as a surfactant-free, scalable synthesis method, its industrial adoption is hindered by empirical trial-and-error approaches and the lack of predictive tools. The current literature offers limited application of machine learning (ML), particularly recommender systems, in PLAL optimization and automation. This study addresses this gap by introducing a ML-based recommender system trained on a 3 × 3 design of experiments with three replicates covering variables, such as fluence (1.83–1.91 J/cm²), ablation time (5–25 min), and laser scan speed (3000–3500 mm/s), in producing magnesium nanoparticles from powders. Multiple ML models were evaluated, including K-Nearest Neighbors (KNN), Extreme Gradient Boosting (XGBoost), Random Forest, and Decision trees. The DT model achieved the best performance for predicting the NP size with a mean percentage error (MPE) of 10%. The XGBoost model was optimal for predicting the NP concentration attaining a competitive MPE of 2%. KNN and Cosine similarity recommender systems were developed based on a database generated by the ML predictions. This intelligent, data-driven framework demonstrates the potential of ML-guided PLAL for scalable, precise NP fabrication in industrial applications. Full article

Introducing small-sized metal nanoparticles directly into biopolymers susceptible to thermal and chemical stimulations remains a significant challenge. Recently, we showed a novel approach to fabricating gold nanoparticles through pulsed laser ablation in liquid (PLAL) using a microchip laser (MCL). Despite its lower pulse energy compared to conventional lasers, this technique demonstrates high ablation efficiency, offering the potential to produce composites without compromising the distinctive structure of biopolymers. As a proof of concept, we successfully generated gelatin-stabilized gold nanoparticles with a smaller size (average diameter of approximately 4 nm), while preserving the unchanged circular dichroism (CD) spectra, indicating the retention of gelatin’s unique structure. Extending this technique to the preparation of type I collagen-stabilized gold nanoparticles yielded non-aggregated nanoparticles, although challenges in yield still persist. These results highlight the potential of the microchip laser ablation technique for producing metal nanoparticles within a vulnerable matrix. Full article

Titanium nitride (TiN) is a candidate material for several plasmonic applications, and pulsed laser ablation in liquids (PLAL) represents a rapid, scalable, and environmentally friendly approach for the large-scale production of nanomaterials with customized properties. In this work, the nanosecond PLAL process is developed, and we provide a concise understanding of the process parameters, such as the solvent and the laser fluence and pulse wavelength, to the size and structure of the produced TiN nanoparticles (NPs). TiN films of a 0.6 μm thickness developed by direct-current (DC) magnetron sputtering were used as the ablation targets. All laser process parameters lead to the fabrication of spherical NPs, while the laser pulse fluence was used to control the NPs’ size. High laser pulse fluence values result in larger TiN NPs (diameter around 42 nm for 5 mJ and 25 nm for 1 mJ), as measured from scanning electron microscopy (SEM). On the other hand, the wavelength of the laser pulse does not affect the mean size of the TiN NPs (24, 26, and 25 nm for 355, 532, and 1064 nm wavelengths, respectively). However, the wavelength plays a vital role in the quality of the produced TiN NPs. Shorter wavelengths result in NPs with fewer defects, as indicated by Raman spectra and XPS analysis. The solvent type also significantly affects the size of the NPs. In aqueous solutions, strong oxidation of the NPs is evident, while organic solvents such as acetone, carbides, and oxides cover the TiN NPs. Full article

The spread of antibiotic-resistant bacteria and the rise of emerging and re-emerging viruses in recent years constitute significant public health problems. Therefore, it is necessary to develop new antimicrobial strategies to overcome these challenges. Herein, we describe an innovative method to synthesize ligand-free silver nanoparticles by Pulsed Laser Ablation in Liquid (PLAL-AgNPs). Thus produced, nanoparticles were characterized by total X-ray fluorescence, zeta potential analysis, transmission electron microscopy (TEM), and nanoparticle tracking analysis (NTA). A 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay was performed to evaluate the nanoparticles’ cytotoxicity. Their potential was evaluated against the enveloped herpes simplex virus type 1 (HSV-1) and the naked poliovirus type 1 (PV-1) by plaque reduction assays and confirmed by real-time PCR and fluorescence microscopy, showing that nanoparticles interfered with the early stage of infection. Their action was also examined against different bacteria. We observed that the PLAL-AgNPs exerted a strong effect against both methicillin-resistant Staphylococcus aureus (S. aureus MRSA) and Escherichia coli (E. coli) producing extended-spectrum β-lactamase (ESBL). In detail, the PLAL-AgNPs exhibited a bacteriostatic action against S. aureus and a bactericidal activity against E. coli. Finally, we proved that the PLAL-AgNPs were able to inhibit/degrade the biofilm of S. aureus and E. coli. Full article

Pulsed laser ablation in liquids (PLAL) is a versatile technique to produce high-purity colloidal nanoparticles. Despite considerable recent progress in increasing the productivity of the technique, there is still significant demand for a practical, cost-effective method for upscaling PLAL synthesis. Here we employ and unveil the fundamentals of multi-beam (MB) PLAL. The MB-PLAL upscaling approach can bypass the cavitation bubble, the main limiting factor of PLAL efficiency, by splitting the laser beam into several beams using static diffractive optical elements (DOEs). A multimetallic high-entropy alloy CrFeCoNiMn was used as a model material and the productivity of its nanoparticles in the MB-PLAL setup was investigated and compared with that in the standard single-beam PLAL. We demonstrate that the proposed multi-beam method helps to bypass the cavitation bubble both temporally (lower pulse repetition rates can be used while keeping the optimum processing fluence) and spatially (lower beam scanning speeds are needed) and thus dramatically increases the nanoparticle yield. Time-resolved imaging of the cavitation bubble was performed to correlate the observed production efficiencies with the bubble bypassing. The results suggest that nanoparticle PLAL productivity at the level of g/h can be achieved by the proposed multi-beam strategy using compact kW-class lasers and simple inexpensive scanning systems. Full article

Pulsed laser ablation in liquids (PLAL) is a colloidal synthesis technique attracting significant interest from the scientific community due to the quality of the nanoparticles being produced. In this type of synthesis protocol, the cavitation bubble plays a vital role during the synthesis of nanoparticles. This work studied the effect of the laser beam power on cavitation bubble lifetime. Three different laser beam power values (5.8 W, 7.5 W and 10.5 W) were used to irradiate a pure nickel target in de-ionized (DI) water to synthesize nickel-based nanoparticles. The optimal repetition rate maximizing the production of nanoparticles was determined by atomic emission spectroscopy for each laser beam power. It was determined that the optimal repetition rate increased exponentially with laser beam power, while the cavitation bubble lifetime decreased logarithmically with the laser beam power. Moreover, the effect of the laser beam power on the cavitation bubble lifetime also had an effect on the size distribution of the nanoparticles being produced; the smallest size distribution was obtained at the highest laser beam power. Full article

The utilization of pulsed laser ablation in liquids (PLALs) for preparing gold nanoparticles (Au NPs) in organic solvents holds immense potential across diverse applications. This study introduces a compact and low-power microchip laser (MCL) system (average power 50 mW; pulse energy 0.5 mJ). Due to its compactness, an MCL is advantageous for easy manipulation in organic laboratories during the production of metal nanoparticles (NPs) for research and development purposes. In this research, poly(N-vinyl-2-pyrrolidone) (PVP) is used as a stabilizing agent for the preparation of Au NPs in organic solvents (CH₂Cl₂, CHCl₃, 2-PrOH, MeCN, DMF, EtOH, NMP, and DMSO). Our experimental results demonstrate that the particle size remains consistent across all the organic solvents. This study explores the productivity of Au NPs in different organic solvents, revealing the necessity of multiple laser pulses to generate Au NPs successfully. This phenomenon, known as the ‘incubation effect,’ is linked to the lower pulse energy in the experimental condition and the thermal conductivity of the solvents. The findings emphasize the crucial role of solvent properties in determining the Au NPs productivity in PLAL. Full article

Bismuth titanate (BTO) nanoparticles were obtained by pulsed laser ablation in liquid media (PLAL). Distilled water, ethanol, isopropanol, and acetone were used as media for laser ablation experiments, in which the colloidal solutions were obtained. Laser ablation was carried out using the second harmonic and fundamental wavelength of a pulsed Nd:YAG laser (532 nm and 1064 nm, respectively) with laser fluences of 25 and 12 mJ/cm², respectively. Transmission electron microscopy was utilized for morphological characterization. BTO nanoparticles obtained have spherical shapes with orthorhombic structure and the average size distribution depended on the liquid media nature. In alcohols, BTO NPs were spherical with a carbon layer around them. X-ray diffraction, UV-Vis absorption spectra, and X-ray photoelectron spectroscopy were used to confirm the structural, optical, and elemental properties of the ablated products. The presented results show that PLAL is a viable technique for the synthesis of high-quality BTO nanoparticles with enhanced optical properties for possible applications in photocatalysis. Full article

Laser synthesis of polyyne molecules C${}_{2n}$H${}_2$ (n > 2) in liquid hydrocarbons is a complex process in which intense pulsed radiation decomposes the initial carbon-containing substance (the hydrocarbon solvent itself or the solid carbon particles in a suspension). Notwithstanding the fact that the mechanism of pulsed laser ablation in liquids (PLAL) is widely accepted, the effect of the laser parameters on laser-driven polyyne formation is still not understood in detail. Here, we report a study of the polyyne yield as a function of the laser field intensity and exposure dose. Several carbon-containing liquids, including pure n-hexane, pure ethanol, and graphite powder suspended in ethanol, were treated with tightly focused picosecond IR radiation (wavelength of 1064 nm, pulse duration of 10 ps). The synthesis rate was characterized by UV-vis optical absorption spectroscopy. The yields of the polyynes were found to vary in exact accordance with the value of the absorbed laser energy, following specific nonlinear or linear laws. The influence of the laser intensity on the partial concentration of polyynes in the solution was analyzed. Full article

The production of non-toxic and homogeneous colloidal solutions of nanoparticles (NPs) for biomedical applications is of extreme importance nowadays. Among the various methods for generation of NPs, pulsed laser ablation in liquids (PLAL) has proven itself as a powerful and efficient tool in biomedical fields, allowing chemically pure silicon nanoparticles to be obtained. For example, laser-synthesized silicon nanoparticles (Si NPs) are widely used as contrast agents for bio visualization, as effective sensitizers of radiofrequency hyperthermia for cancer theranostics, in photodynamic therapy, as carriers of therapeutic radionuclides in nuclear nanomedicine, etc. Due to a number of complex and interrelated processes involved in the laser ablation phenomenon, however, the final characteristics of the resulting particles are difficult to control, and the obtained colloidal solutions frequently have broad and multimodal size distribution. Therefore, the subsequent fragmentation of the obtained NPs in the colloidal solutions due to pulsed laser irradiation can be utilized. The resulting NPs’ characteristics, however, depend on the parameters of laser irradiation as well as on the irradiated material and surrounding media properties. Thus, reliable knowledge of the mechanism of NP fragmentation is necessary for generation of a colloidal solution with NPs of predesigned properties. To investigate the mechanism of a laser-assisted NP fragmentation process, in this work, we perform a large-scale molecular dynamics (MD) modeling of FS laser interaction with colloidal solution of Si NPs. The obtained NPs are then characterized by their shape and morphological properties. The corresponding conclusion about the relative input of the properties of different laser-induced processes and materials to the mechanism of NP generation is drawn. Full article

Spherical copper oxide nanoparticles (CuO/Cu₂O NPs) were synthesized by pulsed laser ablation in liquids (PLAL). The copper target was totally submerged in deionized (DI) water and irradiated by an infrared laser beam at 1064 nm for 30 min. The NPs were then characterized by dynamic light scattering (DLS) and atomic emission spectroscopy (AES) to determine their size distribution and concentration, respectively. The phases of copper oxide were identified by Raman spectroscopy. Then, the antibacterial activity of CuO/Cu₂O NPs against foodborne pathogens, such as Salmonella enterica subsp. enterica serotype Typhimurium DT7, Escherichia coli O157:H7, Shigella sonnei ATCC 9290, Yersinia enterocolitica ATCC 27729, Vibrio parahaemolyticus ATCC 49398, Bacillus cereus ATCC 11778, and Listeria monocytogenes EGD, was tested. At a 3 ppm concentration, the CuO/Cu₂O NPs exhibited an outstanding antimicrobial effect by killing most bacteria after 5 h incubation at 25 °C. Field emission scanning electron microscope (FESEM) confirmed that the CuO/Cu₂O NPs destructed the bacterial cell wall. Full article

We report the design, fabrication, and testing of a humidity sensor based on an optical fiber-based evanescent wave probe. The fiber was bent into a U-shape and de-cladded at the location of the bending. The de-cladded section was coated either with Au or with ZnO nanoparticles. Humidity is detected based on the interaction in the surface plasmon resonance of the Au/ZnO nanoparticles excited by an evanescent wave of light passing through the optical fiber. The response of the U-bent fibers to humidity was investigated using a specifically designed low-voltage portable interrogation box. We found that the fibers coated with ZnO nanoparticles were able to detect a minimum 0.1% change in humidity with an average sensitivity of 143 µV/%RH and 95% linearity over the 10% to 80% humidity range. In comparison, samples coated with Au and Au + ZnO nanoparticles demonstrated a minimum change detection of 0.3% RH and 2% RH respectively. The response and recovery time of the sensor were measured to be 3 s and 4 s, respectively, for a 60% change in humidity from 20% to 80%. The entire measurement system was operated by consuming an electrical power of 1.62 W at an input voltage of 12 Vdc. Full article