Femtosecond Laser Research Articles

Preparation of Large Wide Cross Sections of Electronic Devices with a Femtosecond Laser for SEM Imaging

Preparation of Large Wide Cross Sections of Electronic Devices with a Femtosecond Laser for SEM Imaging

Spectrum design of multimode fiber Bragg gratings based on suppression of mode coupling

The direct femtosecond laser inscription method is very competitive in the fabrication of fiber Bragg gratings, but its refractive index modification region is very limited and leads to low reflectivity and wide spectra of multimode fiber gratings. In this work, the relationship between the refractive index modification region, the coupling coefficient, and the spectrum of the multimode fiber grating is investigated based on the intrinsic mechanism of mode coupling; thus the annular and eccentric elliptic refractive index modification regions are accordingly proposed to suppress mode couplings in the multimode fiber Bragg grating, so as to achieve a highly discrete spectrum and narrow spectrum of the multimode fiber Bragg grating, respectively. This work can provide a solid theoretical foundation for the spectrum design of the multimode fiber Bragg grating, which can be utilized to customize the spectrum according to application scenarios such as optical communication, fiber lasers, filtering, and sensing.

Characterising Spatio-Temporal Coupling of Tightly Focused Femtosecond Laser Pulses in Micro-Structured Dispersive Materials

Characterising Spatio-Temporal Coupling of Tightly Focused Femtosecond Laser Pulses in Micro-Structured Dispersive Materials

Simulations of Femtosecond-Laser Near-Field Ablation Using Nanosphere under Dynamic Excitation

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.

Chemical and UV Durability of Hydrophobic and Icephobic Surface Layers on Femtosecond Laser Structured Stainless Steel

Femtosecond laser processing significantly alters the surface structure and chemical composition, impacting its wetting properties. Post-treatments such as immersion in a hydrocarbon liquid (petrol) or storage in a vacuum can significantly reduce ice adhesion, making the surfaces interesting for anti-ice applications. This study investigates their durability against acetone, ethylene glycol, and UV radiation. The laser-structured surfaces were immersed in the respective liquids for up to 48 h. The results indicate limited durability of the superhydrophobic and icephobic layers when submerged in acetone and ethylene glycol, with more favorable results for petrol treatment than vacuum treatment. Similar results were obtained after 100 h of UV exposure, showing a decrease in superhydrophobic properties and an increase in ice adhesion. However, repeated vacuum treatments conducted after the chemical durability tests revealed the potential for partial recovery of the hydrophobic and icephobic properties. XPS analysis was performed throughout the experiments to evaluate changes in surface chemistry resulting from the post-laser treatments and the durability tests.

Specificity of DNA damage formation induced by femtosecond near-infrared laser filamentation in water

We investigated the deoxyribonucleic acid (DNA) damage induced by laser filamentation, which was generated by focusing femtosecond near-infrared Ti:Sapphire laser light in water at several repetition rates ranging from 1000 Hz to 10 Hz. Using plasmid DNA (pUC19), the single-strand break, double-strand break, nucleobase lesions, and the fragmented DNA were analyzed and quantified by agarose gel electrophoresis. Additionally, the H2O2 concentration after irradiation was determined. We observed that (1) the DNA damage per laser shot and (2) the enzyme-sensitive base lesions per total DNA damage decreased as the laser repetition rate increased. Furthermore, (3) extraordinarily short DNA fragments were likely to be produced, compared with those produced using X-rays, and (4) most OH radicals could be eliminated by recombination to generate H2O2, preventing them from damaging the DNA. The Monte-Carlo simulation of the strand break formation implies that the observed dependency of strand break efficiency on the laser repetition rate is mainly due to diffusion of DNA molecules. These findings quantitatively and qualitatively revealed that an intense laser pulse induces a specific DNA damage profile that is not induced by X-rays, a sparsely ionizing radiation source.

High-Performance Sensing Platform Based on Morphology/Lattice Collaborative Control of Femtosecond-Laser-Induced MXene-Composited Graphene.

Flexible sensors based on laser-induced graphene (LIG) are widely used in wearable personal devices, with the morphology and lattice arrangement of LIG the key factors affecting their performance in various applications. In this study, femtosecond-laser-induced MXene-composited graphene (LIMG) is used to improve the electrical conductivity of graphene by incorporating MXene, a 2D material with a high concentration of free electrons, into the LIG structure. By combining pump-probe detection, laser-induced breakdown spectroscopy (LIBS), and density functional theory (DFT) calculations, the morphogenesis and lattice structuring principles of LIMG is explored, with the results indicating that MXene materials are successfully embedded in the graphene lattice, altering both their morphology and electrical properties. The structural sparsity and electrical conductivity of LIMG composites (up to 3187 Sm-1) are significantly enhanced compared to those of LIG. Based on these findings, LIMG has been used in wearable electronics. LIMG electrodes are used to detect uric acid, with a minimum detection limit of 2.48µM. Additionally, LIMG-based pressure and bending sensors have been successfully used to monitor human limb movement and pulse. The direct in situ femtosecond laser patterning synthesis of LIMG has significant implications for developing flexible wearable electronic sensors.

Model of the Effects of Femtosecond Laser Pulse Energy on the Effective Z-Position of the Resulting Cut after Laser-Induced Optical Breakdown

Presented in this study is a validated semiempirical model of the effects of femtosecond laser pulse energy on the effective z-position of the resulting cut after laser-induced optical breakdown. Different energy levels (for the same spot spacings, i.e., different doses) running from 1.07 × (~60 nJ) to 3.8 × (~215 nJ) of the laser-induced optical breakdown (LIOB) threshold (~56 nJ) were used to perform flat cuts within flat poly(methyl methacrylate) (PMMA) samples at the same nominal focus position (depth within the material). The z-locations of the effective cut and the anterior surface of the PMMA were confocally determined. The difference (PMMA_surface—Cut_plane) was used as a surrogate for the effective shift in the z-position of the cut. A consistent and continuous shift towards less deep cuts was observed for increasing pulse energies. The z-shift spreads by up to 22 µm thinner cuts for the largest pulse energy (3.8× LIOBTh, ~215 nJ). Higher pulse energies seem to significantly reduce the cutting depth. The results for PMMA are in good agreement with the moving LIOB model.

Investigation of microchannels on K24 alloy by femtosecond laser considering the incubation of laser pulse

Investigation of microchannels on K24 alloy by femtosecond laser considering the incubation of laser pulse

Passively harmonic mode-locked GHz U-band femtosecond pulse generation based on soliton self-frequency shift

We demonstrate a GHz U-band fiber laser harnessing soliton self-frequency shift (SSFS). The seed source is a passively harmonic mode-locked (HML) fiber laser based on carbon nanotubes (CNTs) polymer film. By adjusting the pump power and polarization controller (PC) appropriately, the repetition rate can be tuned up to 1.104 GHz with a side mode suppression ratio (SMSR) of 42.5 dB. The seed source with different repetition rates can be frequency shifted from C-band to U-band in a piece of dispersion-shifted fiber (DSF) after amplification. We selected three repetition rates (457.8 MHz, 700.1 MHz, and 1104.1 MHz) and systematically studied the impact of different repetition rates on SSFS. The broad tuning range of wavelengths covering the entire U-band can be obtained by adjusting the pump power of the main amplifier. To the best of our knowledge, the demonstrated laser is the first U-band femtosecond fiber laser based on passively HML with a repetition rate over 1 GHz.

High-temperature boron partitioning and isotope fractionation between basaltic melt and fluid

In the last two decades, boron has gained significance as a geochemical tracer in mantle studies, particularly related to fluid-mediated processes. In our investigation, we explore how boron and its stable isotopes distribute between basaltic melt and hydrous fluid under conditions relevant to magmatic degassing in the shallow crust (1000–1250 °C, 150–250 MPa). We utilized a synthetic MORB-like composition with added boric-acid isotope standard (NIST-SRM951a) and additional trace elements, subjecting it to varying pressure, temperature, and melt-fluid ratios using an internally heated pressure vessel. The B isotope composition in the quenched glasses were determined through femtosecond laser ablation coupled to a multi-collector inductively-coupled-plasma mass spectrometer. Our experiments revealed that, even at the highest temperatures, boron strongly partitions into the fluid phase, accompanied by significant B isotope fractionation. This leads to an enrichment of the heavy B isotope in the fluid, with a constrained Δ11Bmelt-fluid range of -1.7 ± 0.9‰, consistent with ab-initio modeling results. These findings highlight the potential of B isotopes to trace geochemical processes at elevated temperatures with \\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$${\\Delta}^{11}{{B}}_{melt-fluid}=2.913-9.693\\frac{{10}^{6}}{{{T}}^{2}}$$\\end{document}. Our results have implications for predicting the δ11B of degassed, water-bearing basaltic magmas and estimating the B isotope composition of their mantle source.

Investigation of the Replication Quality of Microstructures on Injection Moulded Specimens Made from Recycled Polypropylene Composites Reinforced with Carbon Nanotubes

During the research, functional microstructures were created on the cavity surface of the injection moulding tool using femtosecond laser technology. Automotive-grade polypropylene (PP), as well as its recycled and carbon nanotube-reinforced composites, were used as the raw materials. The replicated structures were examined using confocal microscopy. It is expected that by optimizing the process parameters, the filling of the structured cavity surface with nanocomposite materials can reach a quality level comparable to plastic specimens made from non-reinforced raw materials. The aim is to provide results of scientific and industrial value to demonstrate the influence of the modified mould surface on the flow of the polymer melt and thus on the filling of the injection moulded products.

Terahertz Radiation from Water Molecules Rotated by Femtosecond Laser Field

Terahertz Radiation from Water Molecules Rotated by Femtosecond Laser Field

Photodissociation spectra of single trapped CaOH+ molecular ions.

Molecular ions that are generated by chemical reactions with trapped atomic ions can serve as an accessible testbed for developing molecular quantum technologies. On the other hand, they are also a hindrance to scaling up quantum computers based on atomic ions, as unavoidable reactions with background gases destroy the information carriers. Here, we investigate the single- and two-photon dissociation processes of single CaOH+ molecular ions co-trapped in Ca+ ion crystals using a femtosecond laser system. We report the photodissociation cross section spectra of CaOH+ for single-photon processes at λ = 245-275 nm and for two-photon processes at λ = 500-540 nm. Measurements are interpreted with quantum-chemical calculations, which predict the photodissociation threshold for CaOH+ → Ca+ + OH at 265nm. This result can serve as a basis for dissociation-based spectroscopy for studying the internal structure of CaOH+. The result also gives a prescription for recycling Ca+ ions in large-scale trapped Ca+ quantum experiments from undesired CaOH+ ions formed in the presence of background water vapor.

Peltier-based temperature regulation: A method for performance optimization in solid-state lasers

This article presents a direct method for temperature control in solid-state lasers, where temperature stability is crucial for optimizing the performance and reliability of such lasers. The proposed method utilizes Peltier chips for both cooling and heating the laser crystal to achieve precise temperature regulation.The system design is based on the step response of the open-loop thermal system and employs a proportional-integral (PI) controller for closed-loop temperature control. Comprehensive testing on a femtosecond Titanium-Sapphire Laser (Ti:Sapphire laser) demonstrated that the system is capable of maintaining the desired operating temperature with remarkable stability and efficiency, highlighting its practicality for real-world applications.Method Outline:•Utilization of Peltier chips for precise temperature control.•Estimation of first-order transfer function based on step response.•Implementation of a proportional-integral (PI) controller for closed-loop temperature regulation.

Micro-to-Nanoscale Characterization of Femtosecond Laser Photo-Inscribed Microvoids.

Fiber Bragg gratings are key components for optical fiber sensing applications in harsh environments. This paper investigates the structural and chemical characteristics of femtosecond laser photo-inscribed microvoids. These voids are at the base of type III fs-gratings consisting of a periodic array of microvoids inscribed at the core of an optical fiber. Using high-resolution techniques such as quantitative phase microscopy, electron transmission microscopy, and scattering-type scanning near-field IR optical microscopy, we examined the structure of the microvoids and the densified shells around them. We also investigated the high-temperature behavior of the voids, revealing their evolution in size and shape under step isochronal annealing conditions up to 1250 °C.

Effect of monolayer ratio on single-shot all-optical switching in Gd/Fe multilayers

Ultrafast thermally induced magnetization switching (TIMS) with femtosecond lasers has attracted much attention due to its ability to trigger a single switching on the picosecond time scale. Currently, most of the studies on TIMS have focused on various ferrimagnetic alloys. In this paper, TIMS of Gd/Fe multilayers in different monolayer ratios is investigated by atomic spin dynamics. The results show that an increase in the monolayer Gd ratio narrows the energy density window of the switching. Further studies found that a lower damping ratio decreases the laser energy density threshold for magnetization reversal. Moreover, reducing the ratio of Gd in the monolayer at the appropriate energy density can shorten the duration of the transient ferromagnetic-like state, which can lead to faster realization of TIMS. Our simulation results provide new insights to explore the physical mechanism of TIMS in Gd/Fe multilayers.

Evaluation of In Vitro Serotonin-Induced Electrochemical Fouling Performance of Boron Doped Diamond Microelectrode Using Fast-Scan Cyclic Voltammetry.

Fast-scan cyclic voltammetry (FSCV) is an electrochemical sensing technique that can be used for neurochemical sensing with high spatiotemporal resolution. Carbon fiber microelectrodes (CFMEs) are traditionally used as FSCV sensors. However, CFMEs are prone to electrochemical fouling caused by oxidative byproducts of repeated serotonin (5-HT) exposure, which makes them less suitable as chronic 5-HT sensors. Our team is developing a boron-doped diamond microelectrode (BDDME) that has previously been shown to be relatively resistant to fouling caused by protein adsorption (biofouling). We sought to determine if this BDDME exhibits resistance to electrochemical fouling, which we explored on electrodes fabricated with either femtosecond laser cutting or physical cleaving. We recorded the oxidation current response after 25 repeated injections of 5-HT in a flow-injection cell and compared the current drop from the first with the last injection. The 5-HT responses were compared with dopamine (DA), a neurochemical that is known to produce minimal fouling oxidative byproducts and has a stable repeated response. Physical cleaving of the BDDME yielded a reduction in fouling due to 5-HT compared with the CFME and the femtosecond laser cut BDDME. However, the femtosecond laser cut BDDME exhibited a large increase in sensitivity over the cleaved BDDME. An extended stability analysis was conducted for all device types following 5-HT fouling tests. This analysis demonstrated an improvement in the long-term stability of boron-doped diamond over CFMEs, as well as a diminishing sensitivity of the laser-cut BDDME over time. This work reports the electrochemical fouling performance of the BDDME when it is repeatedly exposed to DA or 5-HT, which informs the development of a chronic, diamond-based electrochemical sensor for long-term neurotransmitter measurements in vivo.

Transient features of graphitization and nitrogen-vacancy color centers in a diamond fabricated by localization femtosecond laser direct writing

Transient features of graphitization and nitrogen-vacancy color centers in a diamond fabricated by localization femtosecond laser direct writing

Direct lithography of CsPbCl3, CsPbBrxCl3−x and CsCdxPb1−xBr3 perovskite nanocrystals in organic media

The in-situ generation of perovskite nanocrystals within organic media using a femtosecond laser can greatly simplify the sample preparation process and save pulse energy. In this work, three perovskite nanocrystals (PNCs), CsPbCl3, CsPbBrxCl3−x, and CsCdxPb1−xBr3, were generated in situ within organic media using a femtosecond laser. These three perovskite nanocrystals emitted pure blue or blue-green fluorescence under ultraviolet (UV) irradiation. It was also found that by controlling the laser pulse energy, the CsCdxPb1-xBr3 nanocrystals transitioned from green to blue-green fluorescence. Furthermore, we have successfully realized the patterning of these three perovskite nanocrystals in organic media.