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Register a new userLaser-assisted generation of elongated Au nanoparticles and subsequent dynamics of their morphology under pulsed irradiation in water and calcium chloride solutions
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One-step laser generation of Au elongated nanoparticles (NPs) and their successive fragmentation and agglomeration are experimentally studied for the first time. In the present work, laser-assisted formation of Au elongated nanoparticles by ablation of a solid Au (99.99%) target in water was done using a ytterbium-doped fiber laser sources with pulse duration of 200 ns and pulse energy of 1mJ. Extinction spectrum correlating with TEM shows the appearance of absorption signal in red region and near IR-spectrum that corresponds to longitudinal plasmon resonance of electrons in elongated Au NPs. In addition, generated elongated Au nanoparticles were exposed to pulsed laser beam with various pulse energy and laser exposure time. It was found that at early stages of irradiation NPs agglomerate as the NPs chains with size of order of 1 micrometer long. Further laser exposure results in fragmentation of these chains. Possible processes of laser-assisted formation of elongated Au NPs in aqueous solutions of calcium chloride and their subsequent interaction with pulsed laser irradiation are discussed.
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We report the generation of molecular hydrogen from water by laser irradiation, without any electrodes and photocatalysts. A near infrared pulsed nanosecond laser is used for exposure of colloidal solution of Au nanoparticles suspended in water. Laser exposure of the colloidal solution results in formation of plasma of laser breakdown of liquid and emission of H2. The rate of H2 emission depends critically on the energy of laser pulses. There is a certain threshold in laser fluence in liquid (around 50 J/cm2) below which plasma disappears and H2 emission stops. H2 emission from colloidal solution of Au nanoparticles in ethanol is higher than that from similar water colloid. It is found that formation of plasma and emission of H2 or D2 can be induced by laser exposure of pure liquids, either H2O or D2O, respectively. The results are interpreted as water molecules splitting by direct electron impact from breakdown plasma.
Influence of permanent magnetic field up to 7.5 T on plasma emission and laser-assisted Au nanoparticles fragmentation in water is experimentally studied. It is found that presence of magnetic field causes the breakdown plasma emission to start earlier regarding to laser pulse. Field presence also accelerates the fragmentation of nanoparticles down to a few nanometers. Dependence of Au NPs fragmentation rate in water on magnetic field intensity is investigated. The results are discussed on the basis of laser-induced plasma interaction with magnetic field.
Formation of molecular H2 and O2 is experimentally studied under laser exposure of water colloidal solution to radiation of a Nd:YAG laser at pulse duration of 10 ns and laser fluence in the liquid of order of 100 J/cm2. It is found the partial pressure of both H2 and O2 first increases with laser exposure time and saturates at exposures of order of 1 hour. The balance between O2 and H2 content depends on the laser energy fluence in the solution and is shifted towards H2 at high fluences. Possible mechanisms of formation of the dissociation products are discussed, from direct dissociation of H2O molecules by electrons of plasma breakdown to emission of laser-induced plasma in liquid.
The heating effect of terahertz pulse with various frequencies and intensities on the heavy water solution is investigated using the molecular dynamics simulation. Resonant absorptions are found for both heavy water and light water, but at a different resonant frequency which is about 16 THz for heavy water and 21 THz for light water. This resonant phenomenon can be explained perfectly by the collective rotational modes that may release water molecules from hydrogen bonding. The findings not only illustrate the heating mechanism of heavy water solution under the terahertz pulse irradiation, but also demonstrate a novel difference between light water and heavy water that could have potential applications.
The dynamic processes in the surface layers of metals subjected activity of a pulsing laser irradiation, which destroyed not the crystalline structure in details surveyed. The procedure of calculation of a dislocation density generated in bulk of metal during the relaxation processes and at repeated pulse laser action is presented. The results of evaluations coincide with high accuracy with transmission electron microscopy dates. The dislocation-interstitial mechanism of laser-stimulated mass-transfer in real crystals is presented on the basis of the ideas of the interaction of structure defects in dynamically deforming medium. The good compliance of theoretical and experimental results approves a defining role of the presented mechanism of mass transfer at pulse laser action on metals. The possible implementation this dislocation-interstitial mechanism of mass transfer in metals to other cases of pulsing influences is justified
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