Femtosecond laser-induced optical breakdown in liquids results in filamentation, which involves the formation and collapse of bubbles. In the present work, we elucidate spatio-temporal evolution, interaction, and dynamics of the filamentation-induced bubbles in a liquid pool as a function of a broad spectrum of laser pulse energies (∼1 to 800 µJ), liquid media (water, ethanol, and glycerol), and the number of laser pulses. Filament attributes such as length and diameter have been demarcated and accurately measured by employing multiple laser pulses and were observed to have a logarithmic dependence on laser energy, irrespective of the medium. The size distribution of persisting microbubbles is controlled by varying the pulse energy and the number of pulses. Our experimental results reveal that introducing consecutive pulses leads to strong interaction and coalescence of the pulsating bubbles via Bjerknes force due to laser-induced acoustic field generation. The successive pulses also influence the population density and size distribution of the micro-bubbles. We also explore the size, shape, and agglomeration of bubbles near the focal region by controlling the laser energy for different liquids. The insights from this work on filamentation-induced bubble dynamics can be of importance in diverse applications such as surface cleaning, fluid mixing and emulsification, and biomedical engineering.
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http://dx.doi.org/10.1038/s41598-022-20066-1 | DOI Listing |
Talanta
December 2024
Institute of Atomic and Molecular Physics, Jilin University, Changchun, 130012, China. Electronic address:
Laser-induced breakdown spectroscopy (LIBS) is a rapidly evolving in-situ multi-element analysis technique that has significantly advanced the field of liquid analysis. This study employs a femtosecond laser for quantitative analysis of heavy metals in flowing liquids, exploring its detection sensitivity and accuracy. Femtosecond pulsed laser excitation of water in a dynamic environment generates plasma while effectively preventing liquid splashing.
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December 2024
Institute of Physics and Center for Interdisciplinary Nanostructure Science and Technology (CINSaT), University of Kassel, Heinrich-Plett-Strasse 40, 34132, Kassel, Germany.
The ultrafast ionic dynamics in solids induced by intense femtosecond laser excitation are controlled by two fundamentally different yet interrelated phenomena. First, the substantial generation of hot electron-hole pairs by the laser pulse modifies the interatomic bonding strength and characteristics, inducing nonthermal ionic motion. Second, incoherent electron-ion collisions facilitate thermal equilibration between electrons and ions, achieving a uniform temperature on a picosecond timescale.
View Article and Find Full Text PDFACS Appl Mater Interfaces
December 2024
Institute of Materials Science and Engineering, Chemnitz University of Technology, Erfenschlager Straße 73, Chemnitz 09125, Germany.
The generation of laser-induced periodic surface structures (LIPSS) using femtosecond lasers facilitates the engineering of material surfaces with tailored functional properties. Numerous aspects of their complex formation process are still under debate, despite intensive theoretical and experimental research in recent decades. This particularly concerns the challenge of verifying approaches based on electromagnetic effects or hydrodynamic processes by experiment.
View Article and Find Full Text PDFMicromodification in bulk undoped polymethylmethacrylate (PMMA) by single focused (numerical aperture (NA) = 0.25), 1030-nm 250-fs laser pump pulses was explored by pump self-transmittance; optical, 3D-scanning confocal photoluminescence (PL); Raman micro-spectroscopy; and optical polarimetric and interferometric microscopy. Starting from the threshold pulse energy = 0.
View Article and Find Full Text PDFACS Appl Mater Interfaces
December 2024
Université de Bordeaux, CNRS, Bordeaux INP, ICMCB, UMR 5026, Pessac F-33600, France.
Femtosecond laser inscription in a ytterbium-doped silver-containing phosphate glass is demonstrated by achieving 3D highly localized laser-induced silver photochemistry. The produced fluorescent silver nanoclusters lead to high optical contrast in the visible range, showing that the coinsertion of Yb ions is not detrimental to the silver-based photochemistry. We demonstrate efficient energy transfer from these silver nanoclusters to the rare-earth Yb ions, leading to near-IR background-free fluorescence emission.
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