Femtosecond Laser Pulse Irradiation Research Articles

Effect of dopant concentration on femtosecond pulsed laser irradiation of yttria-stabilized zirconia for generating nanopores

Yttria-stabilized zirconia (YSZ) is a fine ceramics material that has been applied to dental implants and mechanical components. As YSZ is a hard, brittle, and chemically stable material, that undergoes phase transformation during mechanical loading, it is difficult to fabricate nanostructures using mechanical processing methods. In this study, a surface structuring method using a femtosecond pulsed laser was proposed, which is effective in suppressing the mechanical loading-induced phase transformation. As the material properties of YSZ vary with the concentration of yttria dopant, polycrystalline zirconia samples with different yttria concentrations (2, 3, 5, and 8 mol%) were used to investigate the effect of yttria concentrations on laser processing characteristics for nanostructuring. At all concentrations, nanopore generation in the surface grain was achieved by laser irradiation near the ablation threshold. In addition, there was no significant change in the crystal structure before and after laser irradiation, and no damage to the bulk occurred. At 2 mol%, intergranular cracks were generated around the pores. By increasing the dopant level to 5 mol%, the lens effect of the crystal grains became stronger due to enhanced grain growth, and the diameter and number of pores increased. In addition, pores formed preferentially on smaller grains at 5 mol%. However, for YSZ with 8 mol%, the pore formation phenomenon was different from that in the lower dopant level, as the area near the grain boundary was preferentially ablated, and microcracks formation and exfoliation of the surface also occurred. These results contribute to a deeper understanding of the laser ablation characteristics of zirconia with different dopant levels and to the development of surface structuring methods for fine ceramics materials.

Protector-free, non-plasmonic silver quantum clusters by femtosecond pulse laser irradiation: in situ binding on nanocellulose filaments for improved catalytic activity and cycling performance.

This study introduces a new, facile method to synthesize silver clusters from aqueous silver ion solution by using high intensity femtosecond pulse laser irradiation. The particles obtained in the absence of reducing or capping agents are 1-17 nm in size and presented quantum properties, as characterized by fluorescence, but did not exhibit plasmon signals, which is not a common characteristic of conventional silver nanoparticles. In a further development, small silver quantum clusters (∼1 nm) were bound in situ to wet-spun filaments of cellulose nanofibrils by pulsed laser irradiation. The obtained hybrid filaments as well as free silver quantum clusters revealed a catalytic activity remarkably higher than that of free gold quantum clusters; moreover, the hybrid filaments were found to show improved stability and cycling performance for silver-based catalysis. The present results indicate the potential of femtosecond laser irradiation to generate clusters as well as hybrid systems with excellent performance and reactivity.

Femtosecond Pulsed Laser Irradiation of Zirconia for Embedding Silver Nanoparticles in Surface Nanopores

Femtosecond pulsed laser irradiation was performed to investigate the feasibility and fundamental characteristics of embedding silver nanoparticles onto zirconia ceramic surfaces. By irradiating laser, nanopores were fabricated on the surface of the yttria-stabilized zirconia (YSZ) substrate, and silver nanoparticles were infiltrated and immobilized into the pores using a commercial nano-silver dispersion solution. Numerous nanopores embedded with silver nanoparticles were successfully obtained on the YSZ surface while keeping the grains’ shapes unchanged by controlling laser parameters. Optimizing laser fluence and scanning speed near the ablation threshold made it possible to remove only the excess dispersant that remained on the surface while keeping silver in the pores and without causing machining of the surface of the YSZ substrate. In addition, about 60% embedding in the nanopores was achieved. It was found that the shorter pulse width was suitable to avoid evaporating both dispersant and silver. Cross-sectional observation revealed that the silver nanoparticles were agglomerated to form clumps and were embedded without a gap at the bottom of the pores at a depth of about 600 nm. After laser irradiation, no significant laser-induced phase change was observed in the YSZ substrate, indicating that there was no in-process thermal damage to the bulk. These findings demonstrated the possibility of adding a metal nanoparticle to the zirconia surface by using only a laser process without damaging the properties of the base material during the process. New applications of zirconia, such as the generation of functional surfaces with antibacterial properties, are expected.

From Multi- to Single-Hollow Trimetallic Nanocrystals by Ultrafast Heating.

Metal nanocrystals (NCs) display unique physicochemical features that are highly dependent on nanoparticle dimensions, anisotropy, structure, and composition. The development of synthesis methodologies that allow us to tune such parameters finely emerges as crucial for the application of metal NCs in catalysis, optical materials, or biomedicine. Here, we describe a synthetic methodology to fabricate hollow multimetallic heterostructures using a combination of seed-mediated growth routes and femtosecond-pulsed laser irradiation. The envisaged methodology relies on the coreduction of Ag and Pd ions on gold nanorods (Au NRs) to form Au@PdAg core-shell nanostructures containing small cavities at the Au-PdAg interface. The excitation of Au@PdAg NRs with low fluence femtosecond pulses was employed to induce the coalescence and growth of large cavities, forming multihollow anisotropic Au@PdAg nanostructures. Moreover, single-hollow alloy AuPdAg could be achieved in high yield by increasing the irradiation energy. Advanced electron microscopy techniques, energy-dispersive X-ray spectroscopy (EDX) tomography, X-ray absorption near-edge structure (XANES) spectroscopy, and finite differences in the time domain (FDTD) simulations allowed us to characterize the morphology, structure, and elemental distribution of the irradiated NCs in detail. The ability of the reported synthesis route to fabricate multimetallic NCs with unprecedented hollow nanostructures offers attractive prospects for the fabrication of tailored high-entropy alloy nanoparticles.

Study on the laser-induced damage characteristics and structure changes of fluorotellurite glass under femtosecond pulsed laser irradiation

TeO2-ZnF2-BaF2-Ta2O5 fluorotellurite glasses have excellent optical properties and stability which makes them promising candidates for mid-infrared (mid-IR) fiber applications. In this work, the properties and structure of fluorotellurite glasses with gradient change of BaF2 content were compared. Under the irradiation of femtosecond (fs) laser, the potential relationship between fs laser-induced damage characteristics, glass composition and structural property were systematically studied. The fs laser-induced damage threshold (FLIDT) of investigated fluorotellurite glass samples increased from 892.45 mJ/cm2 by more than one-third to 1223.84 mJ/cm2 and the attenuation coefficient of multi-pulse FLIDT increases from 7.69 to 25.29 with the increase of [TeO3] content from 0.312 to 0.565 induced by increasing BaF2 content. Further, structural transformation from TeO4 units to TeO3 units in the glass network triggered by fs laser irradiation is confirmed by Raman spectra measurements. This study provides theoretical guidance for tailoring the fs laser damage threshold through glass microstructural modulation by composition optimization, which is of great importance to improve the output power in mid-IR supercontinuum (SC) spectra and rare earth (RE) doped fiber laser systems.

Sub-nanometer scale depth patterning on sapphire crystal by femtosecond soft x-ray laser pulse irradiation.

Damage thresholds and structures on a metal aluminum and an aluminum oxide crystal induced by the soft x-ray free electron laser irradiations were evaluated. Distinctive differences in damage thresholds and structures were observed for these materials. On the aluminum oxide crystal surface, in particular, a novel, to the best of our knowledge, surface processing, which we suggest defining as "peeling," was recognized. Surface structures formed by peeling had extremely shallow patterning of sub-nanometer depth. For the newly observed peeling process, we proposed a scission of chemical bond, i.e., binding energy model, in the crystal.

Thermal dynamics of gold nanoshell dimers under femtosecond laser pulse irradiation: A numerical approach.

We present a numerical investigation of the photothermal response of gold nanoshell (AuNS) dimers when subjected to femtosecond laser pulse irradiation. The time-varying temperature fields for core-shell AuNS dimers are quantified by implementing finite element modeling, integrating the electromagnetic and thermal dual-physics simulations. Given the ultrafast nature of laser pulses, we employ a two-temperature model to accurately portray the energy transfer from excited electrons to the lattice system, a process typically completed post pulse-termination. The temporal analysis of the temperature in the AuNS and the surrounding medium, together with the spatial temperature distribution under different separation distances, elucidates the processes that drive the AuNS dimers' transient temperature distribution and heat dissipation. We report on the critical effects of geometrical parameters on the photothermal response, demonstrating that thinner shells maximize the total deposited energy per unit volume, resulting in increased temperature fields, while decreasing separation distances result in excessive field amplification due to plasmonic modes' production. Our robust numerical approach, enabling simulations with tunable material properties and configurations, may help design nanomaterials with desired features for photothermal cancer treatment and imaging.

Creating zinc-hyperdoped silicon with modulated conduction type by femtosecond laser irradiation

Silicon, as the earth-abundant semiconductor, has low cost and good compatibility with mature complementary metal-oxide-semiconductor technology. Therefore, instead of choosing the proper semiconductor with a specific bandgap energy, hyperdoping technique, which can introduce deep-level dopants and intermediate band into silicon, enable silicon to operate in infrared wavebands. Particularly, the hyperdoped silicon with transition metals, having low ionized impurity scatting, makes silicon a promising infrared detection material. In present work, zinc-hyperdoped silicon is fabricated by femtosecond pulsed laser irradiation. The doping concentration of zinc has exceeded 1019 cm−3, and even reached 1022 cm−3, which is about five orders of magnitude greater than the solid solubility of zinc in crystalline Si. The zinc-hyperdoped silicon shows sub-bandgap absorptance of 87.86 % at 1310 nm. Temperature-dependent Hall effect measurements prove that zinc doping results in acceptor energy level located at 0.520 eV above the valence band maximum. It is worth nothing that, zinc-oxygen related defect state results in donor energy level located at 0.252 eV below the conduction band minimum when lower laser fluence is used, which means the energy level of impurity is altered by the presence of undesignedly doped oxygen atoms, suggesting compound formation between the zinc atoms and oxygen atoms.

Emodin‐Based Nanoarchitectonics with Giant Two‐Photon Absorption for Enhanced Photodynamic Therapy

AbstractTwo‐photon‐excited photodynamic therapy (TPE‐PDT) has significant advantages over conventional photodynamic therapy (PDT). However, obtaining easily accessible TPE photosensitizers (PSs) with high efficiency remains a challenge. Herein, we demonstrate that emodin (Emo), a natural anthraquinone (NA) derivative, is a promising TPE PS with a large two‐photon absorption cross‐section (TPAC: 380.9 GM) and high singlet oxygen (1O2) quantum yield (31.9 %). When co‐assembled with human serum albumin (HSA), the formed Emo/HSA nanoparticles (E/H NPs) possess a giant TPAC (4.02×107 GM) and desirable 1O2 generation capability, thus showing outstanding TPE‐PDT properties against cancer cells. In vivo experiments reveal that E/H NPs exhibit improved retention time in tumors and can ablate tumors at an ultra‐low dosage (0.2 mg/kg) under an 800 nm femtosecond pulsed laser irradiation. This work is beneficial for the use of natural extracts NAs for high‐efficiency TPE‐PDT.

Emodin-Based Nanoarchitectonics with Giant Two-Photon Absorption for Enhanced Photodynamic Therapy.

Two-photon-excited photodynamic therapy (TPE-PDT) has significant advantages over conventional photodynamic therapy (PDT). However, obtaining easily accessible TPE photosensitizers (PSs) with high efficiency remains a challenge. Herein, we demonstrate that emodin (Emo), a natural anthraquinone (NA) derivative, is a promising TPE PS with a large two-photon absorption cross-section (TPAC: 380.9 GM) and high singlet oxygen (1 O2 ) quantum yield (31.9 %). When co-assembled with human serum albumin (HSA), the formed Emo/HSA nanoparticles (E/H NPs) possess a giant TPAC (4.02×107 GM) and desirable 1 O2 generation capability, thus showing outstanding TPE-PDT properties against cancer cells. In vivo experiments reveal that E/H NPs exhibit improved retention time in tumors and can ablate tumors at an ultra-low dosage (0.2 mg/kg) under an 800 nm femtosecond pulsed laser irradiation. This work is beneficial for the use of natural extracts NAs for high-efficiency TPE-PDT.

GHz bursts in MHz burst (BiBurst) enabling high-speed femtosecond laser ablation of silicon due to prevention of air ionization

For the practical use of femtosecond laser ablation, inputs of higher laser intensity are preferred to attain high-throughput material removal. However, the use of higher laser intensities for increasing ablation rates can have detrimental effects on ablation quality due to excess heat generation and air ionization. This paper employs ablation using BiBurst femtosecond laser pulses, which consist of multiple bursts (2 and 5 bursts) at a repetition rate of 64 MHz, each containing multiple intra-pulses (2–20 pulses) at an ultrafast repetition rate of 4.88 GHz, to overcome these conflicting conditions. Ablation of silicon substrates using the BiBurst mode with 5 burst pulses and 20 intra-pulses successfully prevents air breakdown at packet energies higher than the pulse energy inducing the air ionization by the conventional femtosecond laser pulse irradiation (single-pulse mode). As a result, ablation speed can be enhanced by a factor of 23 without deteriorating the ablation quality compared to that by the single-pulse mode ablation under the conditions where the air ionization is avoided.

Nanoscale local modification of PMMA refractive index by tip-enhanced femtosecond pulsed laser irradiation

Tip-enhanced optical effects have enabled a wide palette of nanoscale investigation techniques and recently they were successfully used to modify and manipulate matter with nanoscale spatial resolution. We contribute to this latter area by reporting a viable method to modify the refractive index of polymethyl methacrylate (PMMA). Local surface changes of the refractive index are accomplished by focusing a femtosecond pulsed near-infrared laser beam on the apex of a metalized nanosized tip, traditionally used in scanning probe microscopy (SPM). The refractive index is changed over a circular area with diameter <200 nm under 790 nm illumination, representing a four-fold increase in resolution compared to the current state-of-the-art. These results are obtained at low laser pulse energies (<0.5 nJ), which represents a two orders of magnitude advantage over previously reported methods. Besides enabling modifications of the refractive index with high lateral resolution, this method can pave the way towards other important applications such the fabrication of photonic crystal lattices and surface waveguides.

Formation of Laser-Induced Periodic Surface Structures on Reaction-Bonded Silicon Carbide by Femtosecond Pulsed Laser Irradiation

Reaction-bonded silicon carbide (RB-SiC) is an excellent engineering material with high hardness, stiffness, and resistance to chemical wear. However, its widespread use is hindered due to the properties mentioned above, making it difficult to machine functional surface structures through mechanical and chemical methods. This study investigated the fundamental characteristics of laser-induced periodic surface structures (LIPSSs) on RB-SiC via femtosecond pulsed laser irradiation at a wavelength of 1028 nm. Low-spatial-frequency LIPSS (LSFL) and high-spatial-frequency LIPSS (HSFL) formed on the surface along directions perpendicular to the laser polarization. SiC grains surrounded by a large amount of Si show a reduced threshold for LIPSS formation. By varying laser fluence and scanning speed, HSFL–LSFL hybrid structures were generated on the SiC grains. Transmission electron microscopy observations and Raman spectroscopy were carried out to understand the formation mechanism of the hybrid LIPSS. A possible mechanism based on the generation of multiple surface electromagnetic waves due to the nonlinear response of SiC was proposed to explain the hybrid structure formation. Furthermore, the direction of laser scanning with respect to laser polarization affects the uniformity of the generated LIPSS.

Creation of NV centers over a millimeter-sized region by intense single-shot ultrashort laser irradiation

Recently, ultrashort laser processing has attracted attention for creating nitrogen-vacancy (NV) centers because this method can create single NV centers in spatially-controlled positions, which is an advantage for quantum information devices. On the other hand, creating high-density NV centers in a wide region is also important for quantum sensing because the sensitivity is directly enhanced by increasing the number of NV centers. A recent study demonstrated the creation of high-density NV centers by irradiating femtosecond laser pulses, but the created region was limited to micrometer size, and this technique required many laser pulses to avoid graphitization of diamond. Here, we demonstrate the creation of NV centers in a wide region using only an intense single femtosecond laser pulse irradiation. We irradiated a diamond sample with a femtosecond laser with a focal spot size of 41 µm and a laser fluence of up to 54 J/cm2, which is much higher than the typical graphitization threshold in multi-pulse processing. We found that single-pulse irradiation created NV centers without post-annealing for a laser fluence higher than 1.8 J/cm2, and the region containing NV centers expanded with increasing laser fluence. The diameter of the area was larger than the focal spot size and reached over 100 µm at a fluence of 54 J/cm2. Furthermore, we demonstrated the NV centers’ creation in a millimeter-sized region by a single-shot defocused laser pulse over 1100 µm with a fluence of 33 J/cm2. The demonstrated technique will bring interest in the fundamentals and applications of fabricating ultrahigh-sensitivity quantum sensors.

Surface Nanotexturing of Boron-Doped Diamond Films by Ultrashort Laser Pulses.

Polycrystalline boron-doped diamond (BDD) films were surface nanotextured by femtosecond pulsed laser irradiation (100 fs duration, 800 nm wavelength, 1.44 J cm-2 single pulse fluence) to analyse the evolution of induced alterations on the surface morphology and structural properties. The aim was to identify the occurrence of laser-induced periodic surface structures (LIPSS) as a function of the number of pulses released on the unit area. Micro-Raman spectroscopy pointed out an increase in the graphite surface content of the films following the laser irradiation due to the formation of ordered carbon sites with respect to the pristine sample. SEM and AFM surface morphology studies allowed the determination of two different types of surface patterning: narrow but highly irregular ripples without a definite spatial periodicity or long-range order for irradiations with relatively low accumulated fluences (<14.4 J cm-2) and coarse but highly regular LIPSS with a spatial periodicity of approximately 630 nm ± 30 nm for higher fluences up to 230.4 J cm-2.

Generation of nanopore structures in yttria-stabilized zirconia by femtosecond pulsed laser irradiation

Femtosecond pulsed laser irradiation of yttria-stabilized zirconia (YSZ) was performed to investigate the feasibility and fundamental characteristics of nanopore structure fabrication. Numerous nanopores were successfully generated on the YSZ surface with only a single laser pulse shot by controlling laser power near the ablation threshold. The nanopore generation mechanism involves light focusing by the convex shape of a crystal grain and ablation inside the grain. By increasing laser power, the number of nanopores increased. Cross-sectional observation revealed that the depth of nanopores was about 500 nm, and nanopores were generated inside the YSZ grains of the top layer while keeping the grains' shapes unchanged. It was found that higher scanning speed and a small number of scans enabled nanopores fabrication without changing the original surface shape, avoiding the removal of the surface layer. Laser-irradiated surfaces of YSZ were characterized by Raman spectroscopy, and it was found that there was no significant phase change in the specimen after nanopore generation compared with the original YSZ surface, confirming that there was no thermal damage to the bulk material. The surface with nanopores showed an enhancement in surface hydrophilicity. These findings demonstrated the possibility of selectively generating nanopores in the top surface of YSZ for use in functional surfaces without serious thermal damage to the workpiece. It is expected that the nanopore generation will lead to new applications of YSZ.

Formation of NV centers in diamond by a femtosecond laser single pulse.

The NV centers in a diamond were successfully created by the femtosecond laser single pulse. We also investigated the effect on the diamond lattice induced by the different laser pulse widths from both experimental and theoretical perspectives. Interestingly, in spite of the high thermal conductivity of a diamond, we found that there is a suitable pulse repetition rate of several tens kHz for the formation of NV center ensembles by the femtosecond laser pulse irradiation.

Ultrafast control of conductivity with femtosecond lasers - INVITED

Femtosecond laser pulse irradiation enables precise control of conductivity in materials, revolutioniz-ing fields like nanoelectronics and materials science. It offers rapid modulation within femtosecond timescales, facilitating advancements in ultrafast electronics and high-speed data processing. In this talk, we will focus on the photoinduced reduction of conductivity in incommensurate crystals through excitation of electrons into localized states, revealing potential applications in optoelectronics, ultrafast switches, and photonic devices.

Influence of film thickness and substrate roughness on the formation of laser induced periodic surface structures in poly(ethylene terephthalate) films deposited over gold substrates

A study of the formation of Laser Induced Periodic Surface Structures (LIPSS) using near-infrared femtosecond pulsed laser irradiation on poly(ethylene terephthalate) (PET) films deposited over gold substrates has been carried out. We report the influence of the gold substrate roughness and the PET film thickness on LIPSS formation and analyze it in terms of the features of the electric field distribution obtained by computer simulations using COMSOLTM. We obtain LIPSS with periods close to the irradiation wavelength as long as the aforementioned substrate and film parameters remain below certain threshold values, in particular for polymer thicknesses below 200 nm and substrate roughness of few nm. However, experiments show the impossibility of LIPSS formation for rough substrates as well as thick films above these threshold values. In our numerical simulations, we notice the generation of Surface Plasmon Polariton (SPP) in the film-substrate interface that gives rise to a periodical field pattern on the surface of the thin film. This periodicity is broken for a certain level of substrate roughness or film thickness. Moreover, the evolution of the period of the SPP as the substrate roughness and film thickness change for given laser parameters is qualitatively in good agreement with the experimental LIPSS period (below but close to the irradiation laser wavelength). In conclusion, the experimental findings are explained by the formation and behavior of SPP in the thin film-substrate interface. On these grounds, we propose that, for our case of study, this SPP formation and the subsequent inhomogeneous rise in temperature induced by the periodic field on the surface of the sample is the leading mechanism contributing to LIPSS formation.

Ultrafast Temporal-Spatial Dynamics of Phase Transition in N-Doped Ge2Sb2Te5 Film Induced by Femtosecond Laser Pulse Irradiation.

Element-doped phase change material (PCM) could improve the performances, e.g., better thermal stability, higher electrical resistance, and faster crystallization speed; thus, the influence of the doping element needs to be further investigated. In this paper, a femtosecond laser, which could realize the ultrafast phase transition rate of PCM between amorphization and crystallization, was used to explore the properties of nitrogen-doped Ge2Sb2Te5 (GST), and a bond effect was proposed. The pure GST and different nitrogen contents of doped GST films were investigated by femtosecond laser pulse excitation through a pump-probe shadowgraph imaging technique. The results showed that the element-doped films could change photon absorption because of the increase in free carriers. This caused the faster rate of reflectivity to change in the irradiated area by the laser beam as the more nitrogen doped. When the nitrogen content increased, the crystallization evolution became harder because it enhanced the bond effect, which suppressed crystalline grain growth and improved the thermal stability. Based on the analysis in the paper, the desired performances of PCMs, e.g., ultrafast dynamics, crystallization evolution, and thermal stability, could be controlled according to the demands by modifying the bond effect.