Search Results (130)

A reflective in-fiber liquid microsphere whispering gallery mode (WGM) resonator based on a Y-waveguide coupler is proposed and experimentally demonstrated. The sphere resonator is introduced inside a single-mode fiber (SMF) by using femtosecond laser micromachining and fusion splicing. A Y-waveguide coupler is fabricated with femtosecond laser direct writing, which is used to simultaneously excite and collect the WGM field through evanescent field coupling. High-index liquids are filled into the sphere through a laser-drilled channel to form a liquid microsphere where the WGM resonation takes place. The WGM resonator is sensitive to the refractive index (RI) of the filled liquids, and a RI sensitivity of 439 nm/RIU is achieved in an index range from 1.672 to 1.692. The liquid microsphere resonator is also sensitive to temperature, with a sensitivity of −307.1 pm/°C obtained. The microsphere resonator is small in size and robust, which has broad application prospects in the field of food and the chemical industry. Full article

In this article, femtosecond laser scanning was used to create heterojunctions between silver nanowire (Ag NW) and graphene oxide (GO), resulting in a mechanical and electrical interconnection. Surface plasmon resonances (SPRs) were generated on the nanowire surface by using femtosecond laser irradiation, producing a periodically excited electric field along the Ag NWs. This electric field then interfered with the femtosecond laser field, creating strong localized heating effects, which melted the Ag NW and GO, leading to mechanical bonding between the two. The formation of these heterostructures was attributed to the transfer of plasmon energy from the Ag NW to the adjacent GO surface. Since the connection efficiency of the nanowires is closely related to the specific location and the polarization direction of the laser, FDTD simulations were conducted to model the electric field distribution on the surface of Ag NW and GO structures under different laser polarization directions, varying the lengths and diameters of the nanowires. Finally, the resistance changes of the printed Ag NW paths on the GO thin film after femtosecond laser irradiation were investigated. It was found that laser bonding could reduce the resistance of the Ag NW-GO heterostructures by two orders of magnitude, further confirming the formation of the junctions. Full article

This paper focuses on the switching and modulation techniques of terahertz waves, develops ${\mathrm{VO}}_2$ thin-film materials with an SPP structure, and uses terahertz time-domain spectroscopy (THz-TDS) to study the semiconductor–metal phase transition characteristics of ${\mathrm{VO}}_2$ thin films, especially the photoinduced semiconductor–metal phase transition characteristics of silicon-based ${\mathrm{VO}}_2$ thin films. The optical modulation characteristics of silicon-based ${\mathrm{VO}}_2$ thin films to terahertz waves under different light excitation modes, such as continuous light irradiation at different wavelengths and femtosecond pulsed laser irradiation, were analyzed. Combining the optical modulation characteristics of silicon-based ${\mathrm{VO}}_2$ thin films with the filtering characteristics of SPP structures, composite structures of ${\mathrm{VO}}_2$ thin films with metal hole arrays, composite structures of ${\mathrm{VO}}_2$ thin films with metal block arrays, and silicon-based ${\mathrm{VO}}_2$ microstructure arrays were designed. The characteristics of this dual-function device were tested experimentally. The experiment proves that the ${\mathrm{VO}}_2$ film material with an SPP structure has a transmission rate dropping sharply from 32% to 1% under light excitation; the resistivity changes by more than six orders of magnitude, and the modulation effect is remarkable. By applying the SPP structure to the ${\mathrm{VO}}_2$ material, the material can simultaneously possess modulation and filtering functions, enhancing its optical performance in the terahertz band. Full article

This study investigates near-infrared (NIR)-induced, Phyto-enhanced, second harmonic generation-mediated photodynamic therapy (Phyto-SHG-PDT) using barium titanate (BT)/rhein/polyethylene glycol 100 (PEG100) and BT/Yemenite “Etrog” leaf extract/PEG100 nanoconjugates. We compare continuous-wave (CW), multi-line Argon-ion laser illumination in the NIR range with high-peak-power femtosecond (fs) 800 nm pulses. Under CW NIR light, BT/rhein nanoconjugates reduced PC3 prostate cancer cell viability by 18% versus non-irradiated controls (p < 0.05), while BT/extract nanoconjugates exhibited 15% dark toxicity. The observed SHG signal matched theoretical predictions and previous CW laser studies. Reactive Oxygen Species (ROS) scavenger 1,3-diphenyl-isobenzofuran (DPBF) showed reduced absorbance at 410 nm upon NIR illumination, indirectly supporting SHG emission at 400 nm from nanoconjugates. Under fs-pulsed laser exposure, pronounced two-photon absorption (TPA) and SHG effects were observed in both nanoconjugate types. Our results demonstrate the effectiveness of BT/rhein nanoconjugates under both laser conditions, while the BT/extract nanoconjugates benefited from high-power pulsed excitation. These results highlight the potential of BT-based Phyto-SHG-PDT nanoconjugates for NIR and blue light applications, leveraging nonlinear optical effects for advanced photochemical cancer therapies. Full article

Boron nitride nanotubes (BNNTs) are predicted to be promising one-dimensional nonlinear optical materials, but to date, only one experimental observation has been made using individual nanotubes. In this work, second harmonic generation (SHG) was achieved from free-standing bulk BNNT sheets and BNNT coatings on silica substrates. Focusing femtosecond infrared (fs-IR) laser pulses with a wavelength of 800 nm onto the BNNT assemblies resulted in strong SHG at a wavelength of 400 nm. It was observed that due to the thickness variation of the BNNT assemblies and orientational alignment of BNNTs in the assemblies, the intensity of the second-harmonic (SH) radiation changed dramatically when different locations on the samples were investigated. Among all the BNNT assemblies tested, the localized SH response and its dependence on the polarization of the excitation fs-IR pulses were the strongest in BNNT coatings produced by a dip-coating process. By measuring the SH response, the uniformity, reproducibility, and efficiency of BNNT deposition processes could be assessed. For applications requiring a high SH response from BNNT assemblies, the process of dip coating is preferred. Full article

In this report, the nonlinear optical (NLO) properties of titanium dioxide nanoparticles (TiO₂ NPs) have been explored experimentally using femtosecond laser light along with the Z-scan approach. The synthesis of TiO₂ NPs was carried out in distilled water through nanosecond second harmonic Nd:YAG laser ablation. Characterization of the TiO₂ NPs colloids was conducted using UV-visible absorption spectroscopy, transmission electron microscopy (TEM), inductively coupled plasma (ICP), and energy-dispersive X-ray spectroscopy (EDX). The TEM analysis indicated that the size distribution and average particle size of the TiO₂ NPs varied from 8.3 nm to 19.1 nm, depending on the laser ablation duration. The third-order NLO properties of the synthesized TiO₂ NPs were examined at different excitation laser wavelengths and incident powers through both open- and closed-aperture Z-scan techniques, utilizing a laser pulse duration of 100 fs and a high repetition rate of 80 MHz. The nonlinear absorption (NLA) coefficient and nonlinear refractive (NLR) index of the TiO₂ NPs colloidal solutions were found to be influenced by the incident power, excitation wavelength, average size, and concentration of TiO₂ NPs. Maximum values of 4.93 × 10⁻⁹ cm/W for the NLA coefficient and 15.39 × 10⁻¹⁵ cm²/W for the NLR index were observed at an excitation wavelength of 800 nm, an incident power of 0.6 W, and an ablation time of 15 min. The optical limiting (OL) effects of the TiO₂ NPs solution at different ablation times were investigated and revealed to be concentration and average size dependent. An increase in concentration results in a more limiting effect. Full article

Biosensors operating in the terahertz (THz) region are gaining substantial interest in biomedical analysis due to their significant potential for high-sensitivity trace-amount solution detection. However, progress in compact, high-sensitivity chips and methods for simple, rapid and trace-level measurements is limited by the spatial resolution of THz waves and their strong absorption in polar solvents. In this work, a compact nonlinear optical crystal (NLOC)-based reflective THz biosensor with a few arrays of asymmetrical meta-atoms was developed. A near-field point THz source was locally generated at a femtosecond-laser-irradiation spot via optical rectification, exciting only the single central meta-atom, thereby inducing Fano resonance. The reflective resonance response demonstrated dependence on several aspects, including structure asymmetricity, geometrical size, excitation point position, thickness and array-period arrangement. DNA samples were examined using 1 μL applied to an effective sensing area of 0.234 mm² (484 μm × 484 μm) for performance evaluation. The developed Fano resonance sensor exhibited nearly double sensitivity compared to that of symmetrical sensors and one-gap split ring resonators. Thus, this study advances liquid-based sensing by enabling easy, rapid and trace-level measurements while also driving the development of compact and highly sensitive THz sensors for biological samples. Full article

This study presents the development of highly efficient Surface-Enhanced Raman Scattering (SERS) substrates through femtosecond (fs) laser processing of crystalline silicon (Si), resulting in mountain-like microstructures. These microstructures, when decorated with gold nanoparticles (Au NPs), exhibit remarkable SERS performance due to the creation of concentrated hotspots. The enhanced Raman signals originate from the excitation of localized surface plasmon resonance (LSPR) of the Au NPs and the multi-scale rough morphology of the Si substrates. Finite-element method simulations confirm the electromagnetic field enhancement in narrow gaps, supporting the experimental observations. The fabricated substrates show high uniformity, oxidation resistance, long-term stability, and exceptional reproducibility, making them ideal for molecular detection, especially in food safety applications. A remarkable enhancement factor (EF) of 10¹⁰ is attained in the detection of Malachite Green (MG), boasting a limit of detection (LoD) as low as 10⁻¹⁴ M. This underscores the immense potential of this technique for achieving highly sensitive and dependable SERS-based sensing capabilities. Full article

A highly sensitive optical fiber gas pressure sensor with temperature monitoring is proposed and demonstrated. It is based on a slightly tapered fiber with an inner micro-cavity forming an in-fiber Mach–Zehnder interferometer (MZI), and a micro-channel is drilled into the lateral wall of the in-fiber micro-cavity using a femtosecond laser to allow gas to flow in. Due to the dependence of the refractive index (RI) of air inside the micro-cavity on its gas pressure and the high RI sensitivity of the MZI, the device is extremely sensitive to gas pressure. To prevent fiber breakage, the MZI is housed in a silicate capillary tube with an air inlet. Multiple modes are excited by slightly tapering the inner micro-cavity, and the resonance dips in the sensor’s transmission spectrum feature different linear gas pressure and temperature responses, so a sensitivity matrix algorithm can be used to achieve simultaneous demodulation of two parameters, thus resolving the temperature crosstalk. As expected, the experimental results demonstrated the reliability of the matrix algorithm, with pressure sensitivity reaching up to ~−12.967 nm/MPa and temperature sensitivity of ~89 pm/°C. The features of robust mechanical strength and high air pressure sensitivity with temperature monitoring imply that the proposed sensor has good practical and application prospects. Full article

Metallic nanoparticles have gained attention in technological fields, particularly photonics. The creation of silver/gold (Ag/Au) alloy NPs upon laser exposure of an assembly of these NPs was described. First, using the Nd: YAG pulsed laser ablation’s second harmonic at the same average power and exposure time, Ag and Au NPs in distilled water were created individually. Next, the assembly of Ag and Au NP colloids was exposed again to the pulsed laser, and the effects were examined at different average powers and exposure times. Furthermore, Ag/Au alloy nanoparticles were synthesized with by raising the average power and exposure time. The absorption spectrum, average size, and shape of alloy NPs were obtained by using an ultraviolet-visible (UV–Vis) spectrophotometer and transmission electron microscope instrument. Ag/Au alloy NPs have been obtained in the limit of quantum dots (<10 nm). The optical band gap energies of the Ag/Au alloy colloidal solutions were assessed for different Ag/Au alloy NP concentrations and NP sizes as a function of the exposure time and average power. The experimental data showed a trend toward an increasing bandgap with decreasing nanoparticle size. The nonlinear optical characteristics of Ag/Au NPs were evaluated and measured by the Z-scan technique using high repetition rate (80 MHz), femtosecond (100 fs), and near-infrared (NIR) (750–850 nm) laser pulses. In open aperture (OA) Z-scan measurements, Ag, Au, and Ag/AuNPs present reverse saturation absorption (RSA) behavior, indicating a positive nonlinear absorption (NLA) coefficient. In the close-aperture (CA) measurements, the nonlinear refractive (NLR) indices (n₂) of the Ag, Au, and Ag/Au NP samples were ascribed to the self-defocusing effect, indicating an effective negative nonlinearity for the nanoparticles. The NLA and NLR characteristics of the Ag/Au NPs colloids were found to be influenced by the incident power and excitation wavelength. The optical limiting (OL) effects of the Ag/Au alloy solution at various excitation wavelengths were studied. The OL effect of alloy NPs is greater than that of monometallic NPs. The Ag/Au bimetallic nanoparticles were found to be more suitable for optical-limiting applications. Full article

Femtosecond lasers have garnered widespread attention owing to their subdiffraction processing capabilities. However, their intricate natures, involving intrapulse feedbacks between transient material excitation and laser propagation, often present significant challenges for near-field ablation predictions and simulations. To address these challenges, the current study introduces an improved finite-difference time-domain method (FDTD)–plasma model (plasma)–two-temperature model (TTM) framework for simulating the ablation processes of various nanospheres on diverse substrates, particularly in scenarios wherein dynamic and heterogeneous excitations significantly influence optical-field distributions. Initially, FDTD simulations of a single Au nanosphere on a Si substrate reveal that, with transitions in the excitation states of the substrate, the field-intensity distribution transforms from a profile with a single central peak to a bimodal structure, consistent with experimental reports. Subsequently, simulations of a polystyrene nanosphere array on a SiO₂ substrate reveal that different excitation states of the nanospheres yield two distinct modes, namely near-field enhancement and masking. These modes cannot be adequately modeled in the FDTD simulations. Our combined model also considers the intrapulse feedback between the electromagnetic-field distribution resulting from near-field effects and material excitations. Furthermore, the model can quantitatively analyze subsequent electron–phonon coupling and material removal processes resulting from thermal-phase transitions. Consequently, our model facilitates predictions of the femtosecond-laser ablation of single nanospheres or nanosphere arrays with varying sizes and materials placed on substrates subjected to near-field effects. Full article

Laser-induced fluorescence spectroscopy (LIFS) is actively used for remote sensing of atmospheric aerosols and is currently one of the most sensitive and selective techniques for determining small concentrations of substances inside particles. The use of high-power femtosecond laser sources for LIFS-based remote sensing of aerosols contributes to the development of new-generation fluorescence atmospheric lidars since it makes it possible to overcome the energy threshold for the nonlinear-optical effects of multiphoton absorption in particles and receive the emission signal at long distances in the atmosphere. Our study is aimed at the development and experimental demonstration of the technique of nonlinear laser-induced fluorescence spectroscopy (NLIFS) based on the remote excitation of aerosol fluorescent emission stimulated by a spatially structured high-power femtosecond laser pulse. Importantly, for the first time to our knowledge, we demonstrate the advances in using stochastically structured plasma-free intense light channels (postfilaments) specially formed by the propagation of femtosecond laser radiation through a turbulent air layer to improve NLIFS efficiency. A multiple increase in the received signal of two-photon-excited fluorescence of polydisperse-dyed aqueous aerosols by the structured postfilaments is reported. Full article

Femtosecond high-intensity laser pulses at intensities surpassing 10¹⁴ W/cm² can generate a diverse range of functional surface nanostructures. Achieving precise control over the production of these functional structures necessitates a thorough understanding of the surface morphology dynamics with nanometer-scale spatial resolution and picosecond-scale temporal resolution. In this study, we show that single XFEL pulses can elucidate structural changes on surfaces induced by laser-generated plasmas using grazing-incidence small-angle X-ray scattering (GISAXS). Using aluminium-coated multilayer samples we distinguish between sub-picosecond (ps) surface morphology dynamics and subsequent multi-ps subsurface density dynamics with nanometer-depth sensitivity. The observed subsurface density dynamics serve to validate advanced simulation models representing matter under extreme conditions. Our findings promise to open new avenues for laser material-nanoprocessing and high-energy-density science. Full article

Luminescent carbon dots (CDs) were locally synthesized in the core of CYTOP fibers using IR femtosecond laser direct writing (FLDW), a one-step simple method serving as a post-treatment of the pristine fiber. This approach enables the creation of several types of modifications such as ellipsoid voids. The CDs and photoluminescence (PL) distribute at the periphery of the voids. The PL spectral properties were studied through the excitation/emission matrix in the visible range and excitation/emission spectra in the UV/visible range. Our findings reveal the presence of at least three distinct luminescent species, facilitating a broad excitation range extending from UV to green, and light emission spanning from blue to red. The average laser power and dose influence the quantity and ratio of these luminescent CD species. Additionally, we measured the spatially resolved lifetime of the luminescence during and after the irradiation. We found longer lifetimes at the periphery of the laser-induced modified regions and shorter ones closer to the center, with a dominant lifetime ~2 ns. Notably, unlike many other luminophores, these laser-induced CDs are insensitive to oxygen, enhancing their potential for display or data storage applications. Full article

The ability to study chemical dynamics on ultrafast timescales has greatly advanced with the introduction of X-ray free electron lasers (XFELs) providing short pulses of intense X-rays tailored to probe atomic structure and electronic configuration. Fully exploiting the full potential of XFELs requires specialized experimental endstations along with the development of techniques and methods to successfully carry out experiments. The liquid jet endstation (LJE) at the Linac Coherent Light Source (LCLS) has been developed to study photochemistry and biochemistry in solution systems using a combination of X-ray solution scattering (XSS), X-ray absorption spectroscopy (XAS), and X-ray emission spectroscopy (XES). The pump–probe setup utilizes an optical laser to excite the sample, which is subsequently probed by a hard X-ray pulse to resolve structural and electronic dynamics at their intrinsic femtosecond timescales. The LJE ensures reliable sample delivery to the X-ray interaction point via various liquid jets, enabling rapid replenishment of thin samples with millimolar concentrations and low sample volumes at the 120 Hz repetition rate of the LCLS beam. This paper provides a detailed description of the LJE design and of the techniques it enables, with an emphasis on the diagnostics required for real-time monitoring of the liquid jet and on the spatiotemporal overlap methods used to optimize the signal. Additionally, various scientific examples are discussed, highlighting the versatility of the LJE. Full article