Local near field assisted ablation of fused silica

In this contribution we present recent experimental and theoretical results on local near-field assisted laser ablation. Along these lines, we have generated sub-diffraction sized nanostructures on fused silica substrates, exploiting the local near fields of highly ordered triangular gold nanoparticle arrays generated by nanosphere lithography. After preparation, the nanoparticle arrays were irradiated with a single 35 fs long laser pulse with a central wavelength of λ=790 nm. The pulse energy was set to E=3.9 μJ, resulting in a fluence well below the ablation threshold of the fused silica substrates. In addition, 3D electromagnetic simulations using a finite integration technique in time domain have been performed. The simulations demonstrate that indeed the local field in the vicinity of the tips of the triangular nanoparticles overcome the ablation threshold and easily explain the generated nanostructures. Most importantly, the simulations show, that higher order modes contribute to the ablation process. These modes cause ablation along the side edges of the nanoparticles. Finally, we demonstrate, that the optical properties of the triangular nanoparticles, which can be tuned by their morphology, are crucial parameters for the generation of the ablation structures.     

Laser sintering of silver nanoparticle thin films: microstructure and optical properties

We present a method for the sintering of silver (Ag) nanoparticle thin films by millisecond pulsed laser irradiation. The microstructure of sintered thin films and sintering behaviors of nanoparticles were systematically investigated in this paper. Absorption spectra of sintered thin films showed blue-shifted surface plasmon resonances (SPR) from 500 nm to 480 nm and red-shifted from 480 nm to 550 nm when laser power was varied from 100 W to 140 W and from 140 W to 200 W, respectively. This indicates a new technique to control light absorption through joining nanoparticles with laser sintering. According to theoretical calculations based on a heat diffusion model, the melting temperature of these Ag nanoparticles was estimated to be 440 °C during laser irradiation.     

Silver nanoparticles produced by PLD in vacuum: role of the laser wavelength used

In this work we report the results of investigation of silver (Ag) nanoparticles prepared on a silica substrate by laser ablation. Our attention was focused on the mean diameter, size distribution and optical absorption properties of nanoparticles prepared in vacuum by using different laser wavelengths. The fundamental wavelength and the second, third, and fourth harmonics of a nanosecond Nd:YAG laser were used for nanoparticles fabrication. The corresponding values of the laser fluence for each wavelength were: 0.6 J/cm² at 266 nm, 0.8 J/cm² at 355 nm, 2.8 J/cm² at 532 nm, and 2 J/cm² at 1064 nm. The Ag nanoparticles produced have mean diameters in the range from 2 nm to 12 nm as the nanoparticles’ size decreases with the decrease of the wavelength used. The presence of the Ag nanoparticles was also evidenced by the appearance of a strong optical absorption band in the measured UV-VIS spectra associated with surface plasmon resonance (SPR). A redshift and widening of the absorption peak were observed as the laser wavelength was increased. Some additional investigations were performed in order to clarify the structure of the Ag nanoparticles.     

Two-dimensional imaging of atomic and nanoparticle components in copper plasma plume produced by ultrafast laser ablation

We report on the spatial and temporal evolution of the plume generated during ultrafast laser ablation of a pure copper target with 800 nm, ≈50 fs, Ti: Sapphire laser pulses. Time-gated imaging was used to record 2-dimensional images of plume populations. The temporal evolution of neutral (Cu*), and ionic (Cu⁺) components of the plume are separately imaged by exploiting bandpass interference filters, while nanoparticles are investigated by collecting their characteristic broadband emission. The ionic component of the plume moves two to three times faster than the neutral component, with a velocity which is almost independent of laser fluence. Plume emission intensity variations at different fluences and delay times are studied for both atomic and nanoparticle components.     

Synthesis of nanosized particles during laser ablation of gold in water

In this paper we report the formation of gold nanoparticles during laser ablation of gold target in water in the absence of any additives. The experiments were carried out by using the radiation of the pulsed Nd:YAG laser, operating at the second (532 nm, 10 ns, 10 Hz), or the fourth harmonic (266 nm) wavelengths. The properties of the nanoparticles were found to be susceptible to the additional 532 and 266 nm laser irradiation. It has been established that both the mean size of the nanoparticles and their stability could be varied by proper selection of the parameters of laser ablation and postirradiation such as laser fluence and wavelength combinations.     

Subpicosecond excimer laser ablation of thick gold films of ultra-fine particles generated by a gas deposition technique

The results of UV laser ablation of gold nanoparticle films on glass substrates using femtosecond pulses are presented. Films of ultra-fine gold particles were prepared by an inert gas evaporation and deposition technique, resulting in a well-defined log-normal particle size distribution of (7ǃ) nm. The pulse length of the laser was 500 fs at a wavelength of 248 nm. Ablation thresholds, ablation rates at different fluxes, and the morphology of the ablated structures are presented. For the nanoparticle films studied an ablation rate five times higher than that of gold films prepared by the conventional evaporation technique was found. The ablation thresholds and rates are supposed to depend on the particle size and also on the evaporation pressure. These results are explained by taking into account the energy transport properties of nanocrystalline and conventionally evaporated gold films.     

Properties of pulsed laser deposited nanocomposite NiO:Au thin films for gas sensing applications

Nanocomposite thin films formed by gold nanoparticles embedded in a nickel oxide matrix have been synthesized by a new variation of the pulsed laser deposition technique. Two actively synchronized laser sources, a KrF excimer laser at 248 nm and an Nd:YAG laser at 355 nm, were used for the simultaneous ablation of nickel and gold targets in oxygen ambient. The structural, morphological, and electrical properties of the obtained nanocomposite films were investigated in relation to the fluence of the laser irradiating the gold target. The nanocomposite thin films were tested as electrochemical hydrogen sensors. It was found that the addition of the gold nanoparticles increased the sensor sensitivity significantly.     

Laser-assisted generation of gold nanoparticles and nanostructures in liquid and their plasmonic luminescence

Nanoparticles (NPs) and surface nanostructures (NS) are produced via laser ablation of a bulk gold target in liquid using second harmonics of 10 ps Nd:YAG laser (532 nm) with repetition rate of 50 kHz. The morphology and plasmon photoluminescence (PL) properties of obtained nanoscale objects are described. Transmission electron microscopy and field emission scanning electron microscopy are used for morphology characterization of NPs and NS, respectively. Plasmon PL of both gold NPs and NS is experimentally studied using the third harmonics of the Nd:YAG picosecond laser (355 nm) as a pump. The wavelength of intensity maximum of PL of Au NPs colloidal solution virtually coincides with the position of Au NPs plasmon absorption peak. Real-time excitation of both plasmon PL and Raman scattering of surrounding liquid by picosecond laser pulses in aqueous colloidal solution is also investigated. The efficient cross section of plasmon PL of Au NPs colloid is evaluated using Raman scattering of water as a comparative parameter. The results are in good agreement with values obtained in previous works. Plasmon PL from self-organized NS on the Au surface produced via laser ablation is observed for the first time. Its spectrum is compared to PL spectra of both aqueous colloidal solutions of NPs and of NPs deposited on a Si wafer. The obtained experimental data are discussed with reference to the band structure of bulk Au.     

Fabrication of gold nanoparticles in water by laser ablation technique and their characterization

A colloidal solution of gold nanoparticles in deionized nanopure water was produced by laser ablation technique without the use of any chemical/surfactant. Spectral characterization and morphological studies of these nanoparticles were carried out by UV-Vis Spectroscopy and Scanning Electron Microscopy, respectively. A number of variables of the ablating laser pulse have been used to control the size of the fabricated nanoparticles. Excellent correlation between ablating laser pulse parameter and optical and morphological parameters of the gold colloids were obtained. The peak of the extinction spectra shows a monotonic blue shift for laser fluence of 410 J/cm² and above. Below this the extinction peak remains fairly constant in wavelength. Blue shifts of the extinction spectra were also observed with increasing re-ablation time of previously ablated gold colloids. Possible explanations of all these observations are discussed.     

Effect of pulse duration on plasmonic enhanced ultrafast laser-induced bubble generation in water

Bubbles generated in water by focusing femtosecond and picosecond laser pulses in the presence of 100 nm gold nanoparticles have been investigated in the fluence range usually used for efficient cell transfection (100–200 mJ/cm²). Since resulting bubbles are at the nanoscale, direct observation using optical microscopy is not possible. An optical in-situ method has been developed to monitor the time-resolved variation in the extinction cross-section of an irradiated nanoparticle solution sample. This method is used to measure the bubbles lifetime and deduce their average diameter. We show that bubbles generated with femtosecond pulses (40–500 fs) last two times longer and are larger in average than those generated with picosecond pulses (0.5–5 ps). Controlling those bubble properties is necessary for optimizing off-resonance plasmonic enhanced ultrafast laser cell transfection.     

Raman spectroscopy of gold nanoparticles in polycrystalline LiF film

Results of the Raman spectroscopy analysis of a new composite material based on a thin polycrystalline LiF film containing gold nanoparticles are presented. The formation of spherical gold nanoparticles in the film has been confirmed by the X-ray structural analysis and observation of the optical plasmon resonance absorption spectrum with a maximum at 534 nm. The obtained composite layers have been subjected to annealing by ruby laser (λ = 694 nm) in the spectral region on a descending long-wavelength wing of the plasmon absorption band of gold nanoparticles. Raman spectroscopy has been applied for the first time to the investigation of the modification of the shape of gold nanoparticles in LiF during laser annealing. The experimental Raman spectra are compared with calculated modes of in-phase bending vibrations generated in gold nanoparticles.     

Influence of processing time on nanoparticle generation during picosecond-pulsed fundamental and second harmonic laser ablation of metals in tetrahydrofuran

The influence of fundamental and second harmonic wavelength on ablation efficiency and nanoparticle properties is studied during picosecond laser ablation of silver, zinc, and magnesium in polymer-doped tetrahydrofuran. Laser ablation in stationary liquid involves simultaneously the fabrication of nanoparticles by ablation of the target material and fragmentation of dispersed nanoparticles by post irradiation. The ratio in which the laser pulse energy contributes to these processes depends on laser wavelength and colloidal properties. For plasmon absorbers (silver), using the second harmonic wavelength leads to a decrease of the nanoparticle productivity over process time along with exponential decrease in particle diameter, while using the fundamental wavelength results in a constant ablation rate and linear decrease in particle diameter. For colloids made of materials without plasmon absorption (zinc, magnesium), laser scattering is the colloidal property that limits nanoparticle productivity by Mie-scattering of dispersed nanoparticle clusters.     

Luminescence Enhancement from Silica-Coated Gold Nanoparticle Agglomerates Following Multi-photon Excitation

Multi-photon absorption induced luminescence (MAIL) from bare gold nanoparticles, silica-coated particles, as well as silica-coated agglomerated gold nanoparticles suspended in aqueous solution was studied by using time-resolved and steady-state luminescence spectroscopy. The nanoparticles were excited by femtosecond pulses of wavelengths ranging from 630 nm to 900 nm. The luminescence from the particles exhibits a broad spectrum in the UV and VIS region. The time-resolved measurements indicate a luminescence lifetime of a few ps, limited by the response of the experimental system. The studied dependence of the MAIL efficiency on the excitation wavelength showed that the luminescence from silica-coated agglomerates was enhanced over the whole range of excitation wavelengths, when compared to the luminescence from individual gold nanoparticles. The agglomerates show an almost excitation wavelength independent efficiency of the MAIL, while for individual nanoparticles a rapid decrease of the MAIL efficiency was observed with increasing excitation wavelength. The observed enhancement of the MAIL from the agglomerated nanostructures can be attributed to the presence of localized surface plasmon resonances in the spectral region corresponding to the excitation wavelengths. The high MAIL efficiency from the agglomerated nanoparticle structures in the near-infrared could be an advantage in the expanding field of luminescence-based-imaging, as well as in biosensor technology.     

激光烧蚀法制备的纳米金属胶体及表面的特性研究

本文利用Nd∶YAG激光器1064nm激发光照射金、银等贵金属,通过改变激发光的照射时间,制备出各种金、银胶体。对上述胶体进行了透射电镜(TEM)测量金属粒子的尺寸大小及形态表明这些胶体为粒径介于5～25nm的纳米体系,并对该体系进行了紫外—可见—近红外吸收光谱的研究;在制备胶体的同时还获得了纳米级粗糙金属表面,对该表面进行了扫描电镜(SEM)的测量。     

Prism-based Spectral Imaging of Four Species of Single-molecule Fluorophores by Using One Excitation Laser

A prism-based imaging system for simultaneously detecting four species of single-molecule (SM) fluorophores was developed. As for the detection method, four spectrally distinct species of BigDye fluorophores were bound to 50-nm-diameter gold nanoparticles (AuNPs) to form AuNP/BigDye complexes. Four species of complexes were randomly immobilized on different fused-silica slides. BigDyes were excited by an argon-ion-laser (excitation wavelengths: 488 and 514.5 nm) beam through total internal reflection on the slide surface. SM fluorescence emitted from a complex was spectrally dispersed through a prism to form an SM spot elongated in the spectral direction on a charge-coupled device. A scattered light spot generated by the AuNP of the same complex under 594-nm laser illumination was used as a wavelength reference, and the SM fluorescence spectrum was obtained from the pixel-intensity pattern of the elongated SM spot. Peak locations of fluorescence spectra of all the observed SM spots were obtained, and their histograms were distinctly separated according to species. SM spots can thus be classified as one of four species according to their peak locations. By statistically analyzing the histograms, the classification accuracy was estimated to be above 93.8 %. The number of pixels in the spectral direction required for classifying four species of SM fluorophores was estimated to be 10. As for the conventional system (which uses two excitation lasers), 15 pixels are required. Using BigDyes as the four fluorophores (which consist of donors linked to acceptors and can be excited by just an argon-ion laser) is the reason that such a small number of pixels was achieved. The developed system can thus detect 1.5 times more SM fluorophores per field of view; that is, its throughput is 1.5 times higher. The approach taken in this study, namely, using BigDye with a prism-type system, is effective for increasing the throughput of DNA microarray-chip analysis and SM real-time DNA sequencing.     

Elaboration and characterization of bimetallic nanoparticles obtained by laser ablation of Ni75Pd25 and Au75Ag25 targets in water

A YAG laser operating at the second harmonic wavelength (532 nm, 10 Hz, 8 ns and 40 mJ) was used to elaborate bimetallic nanoparticles by laser ablation of Ni₇₅Pd₂₅ and Au₇₅Ag₂₅ targets in water. TEM–EDX, UV–Vis spectroscopy and PIXE measurements were performed to obtain information on their mean sizes, size distributions and chemical composition as a function of the time of laser ablation. The surface of the laser impacted regions of the targets were characterized by RBS in order to check their composition after the laser ablation. The so-obtained bimetallic nanoparticles always show a homogeneous composition. However, while the composition of Au–Ag nanoparticles was found to be very similar to the one of the alloy target, the composition of the Ni–Pd nanoparticles can be different from the nominal composition of the alloy target. Segregation phenomena can be invoked to explain the difference between the Ni–Pd nanoparticles and the Au–Ag nanoparticles compositions obtained in the same conditions. However, an influence of chemical reactions occurring in the high pressure plasma created locally at liquid–solid interface (called ‘reactive quenching’) cannot be completely ruled out.     

Optical and nonlinear optical characteristics of the Ge and GaAs nanoparticle suspensions prepared by laser ablation

The laser ablation of Ge and GaAs targets placed in water and ethanol was carried out using the fundamental radiation of nanosecond Nd:YLF laser. The results of preparation and the optical and nonlinear optical characterization of the Ge and GaAs nanoparticle suspensions are presented. The considerable shift of the band gap energy of the nanoparticles compared to the bulk semiconductors was observed. The distribution of nanoparticle sizes was estimated in the range of 1.5-10 nm on the basis of the TEM and spectral measurements. The nonlinear refractive indices and nonlinear absorption coefficients of Ge and GaAs nanoparticles were defined by the z-scan technique using second harmonic radiation of picosecond Nd:YAG laser (λ = 532 nm).     

The effect of laser wavelength on the ablation rate of carbon

The ablation of graphite is studied as a function of laser fluence for 355, 532 and 1,064 nm wavelength generated by a nanosecond Nd:YAG laser. It has been found that in the case of lower wavelengths, the transition from the thermal ablation to the phase explosion takes place at lower laser fluences. The change of crater shape due to the effect of deep drilling in the proximity of the phase explosion threshold was observed. The calculations of plasma radiation flux to the target surface were made, and the considerable increase of absorbed energy density was found in the case of 355 nm wavelength.     

Soft picosecond X-ray laser nanomodification of gold and aluminum surfaces

Experimental and theoretical investigations of aluminum (Al) and gold (Au) surface modification by soft X-ray laser pulse are presented. Well-polished samples of Al and Au are irradiated by ps-duration pulse with wavelength of 13.9 nm at the energy range of 24–72 nJ. Differences in the melting and the ablation processes for those materials are observed. It is shown that at low laser pulse energy, the nanoscale ripples on the surface may be induced by melting without following ablation. In that case, the nanoscale changes in the surface are caused by splash of molten metal under gradient of fluence. At higher laser pulse energy, the ablation process occurs and craters are formed on the surface. However, the melting determines the size of the modified surface at all ranges of the laser energies. For interpretation of experimental results, the atomistic simulations of melting and ablation processes in Al and Au are provided. The calculated threshold fluencies for melting and ablation are well consistent with measured ones.