Ultraviolet Pulses Research Articles

Circular dichroism in multiphoton ionization of resonantly excited helium ions near channel closing

The circular dichroism (CD) of photoelectrons generated by near-infrared (NIR) laser pulses using multiphoton ionization of excited He+ ions in the 3p(m= +1) state is investigated. The ions were prepared by circularly polarized extreme ultraviolet (XUV) pulses. For circularly polarized NIR pulses co- and counter-rotating relative to the polarization of the XUV pulse, a complex variation of the CD is observed as a result of intensity- and polarization-dependent Freeman resonances, with and without additional dichroic AC-Stark shifts. The experimental results are compared with numerical solutions of the time-dependent Schrödinger equation to identify and interpret the pronounced variation of the experimentally observed CD.

Few-femtosecond time-resolved study of the UV-induced dissociative dynamics of iodomethane

Ultraviolet (UV) light that penetrates our atmosphere initiates various photochemical and photobiological processes. However, the absence of extremely short UV pulses has so far hindered our ability to fully capture the mechanisms at the very early stages of such processes. This is important because the concerted motion of electrons and nuclei in the first few femtoseconds often determines molecular reactivity. Here we investigate the dissociative dynamics of iodomethane following UV photoexcitation, utilizing mass spectrometry with a 5 fs time resolution. The short duration of the UV pump pulse (4.2 fs) allows the ultrafast dynamics to be investigated in the absence of any external field, from well before any significant vibrational displacement occurs until dissociation has taken place. The experimental results combined with semi-classical trajectory calculations provide the identification of the main dissociation channels and indirectly reveal the signature of a conical intersection in the time-dependent yield of the iodine ion. Furthermore, we demonstrate that the UV-induced breakage of the C-I bond can be prevented when the molecule is ionized by the probe pulse within 5 fs after the UV excitation, showcasing an ultrafast stabilization scheme against dissociation.

Inline UV pulse synthesizer

We demonstrated an inline synthesizer for generating ultrashort pulses in the ultraviolet (UV) range. The inline UV pulse synthesizer comprised three nonlinear crystals located in the propagation path of the fundamental driving laser pulse. Second-harmonic signals with central wavelengths of 420, 375, and 345 nm were generated in turn in the three BBO crystals, resulting in a synthesized UV pulse subsequent to the final nonlinear crystal. Its temporal amplitude and phase could be manipulated easily by changing the relative positions of the crystals, allowing for flexibility of the waveform. The minimum pulse duration of the synthesized UV pulse was 4.7 fs, which was close to the Fourier-transform-limited pulse duration. This ultrashort UV pulse with 19 μ\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$\\upmu$$\\end{document}J energy can be utilized in various applications such as high harmonic generation and frustrated tunneling ionization.

Advances in timing and control of ultrafast molecular dynamics: from XUV to infrared

Abstract With the availability of modern laser and detection technologies, the investigation of ultrafast molecular dynamics induced by intense laser pulses has become a routine practice. In this Topical Review, we present a survey of recent progress in the timing and control of ultrafast molecular dynamics, encompassing processes initiated by both extreme ultraviolet and near infrared pulses. Prospects and perspectives of this field are given. This Review underscores the remarkable potential for further advances in understanding and harnessing ultrafast molecular processes.

Elliptically polarized high-order harmonic generation from N[formula omitted]-CO mixed gases

We theoretically study the elliptically polarized high-order harmonic generation from N2-CO mixed gases. Our simulations show that the polarization of HHG is highly sensitive to both the mixing ratio and molecular alignment angle. In particular, even a small addition of CO gas results in a significant enhancement of harmonic ellipticity compared to pure N2 gas. Under a proper mixing ratio and molecular alignment angle, a large ellipticity of HHG is observed, which is larger than that in reported N2-Ar mixture. Furthermore, when considering the molecular alignment effect, the dependence of ellipticity of HHG on mixing ratio exhibits slight variations. These findings pave the way for generating elliptically polarized extreme ultraviolet pulses.

Scheme for generation of spatiotemporal optical vortex attosecond pulse trains

The realization of spatiotemporal vortex structure of various physical fields with transverse orbital angular momentum (OAM) has attracted much attention and is expected to expand the research scope and open new opportunities in their respective fields. Here we present theoretically the first, to the best of our knowledge, study on the generation of attosecond pulse trains featuring a spatiotemporal optical vortex (STOV) structure by a two-color femtosecond light field, with each color carrying transverse OAM. Through careful optimization of relative phase and intensity ratio, we validate the efficient upconversion of the infrared pulse into its tens of order harmonics, showing that each harmonic preserves a corresponding intact topological charge. This unique characteristic enables the synthesis of an extreme ultraviolet attosecond pulse train with transverse OAM. In addition, we reveal that ionization depletion plays an outsize role therein. Our studies pave the way for the generation and utilization of light fields with STOV in the attosecond regime.

Ultraviolet laser-induced fragmentation of hydrocarbon fuel droplets

The present study aims to understand droplet fragmentation due to instabilities from the radiative heating process. We focus on the plasma-induced breakup mechanism of iso-octane and n-hexane droplets from the nucleation of holes through sheets and instabilities. The plasma generation inside the droplets leads to an intense explosion followed by fragmentation of the droplets. A droplet is suspended in the air using an acoustic levitator and exposed to ultraviolet nanosecond laser pulses. The droplet sizes used are in the range of 0.5–2 mm in diameter, and laser energies are 10–20 mJ per pulse. Initially, plasma formation followed by shock wave emission is observed during the impact of the laser pulse. Afterward, the droplet opens at one side and is stretched vertically to form a liquid sheet. The hole formation and its rapid growth result in the breaking of the thin liquid sheet. Small droplets and ligaments emerge from the circular edge of the sheet, which follows the well-known ligament distribution. This study reveals the detailed analysis of expansion dynamics, evolution of single and multiple holes, and instabilities associated with the liquid sheet. The results observed are categorized into four different mechanisms: (1) plasma formation followed by shock wave propagation, (2) droplet deformation, (3) sheet breakup through nucleation of holes followed by rapid growth, and (4) complete atomization.

Versatile Papertronics: Photo-Induced Synapse and Security Applications on Papers.

Paper is a readily available material in nature. Its recyclability, eco-friendliness, portability, flexibility, and affordability make it a favored substrate for researchers seeking cost-effective solutions. Electronic devices based on solution process are fabricated on paper and banknotes using PVK and SnO2 nanoparticles. The devices manufactured on paper substrates exhibit photosynaptic behavior under ultraviolet pulse illumination, stemming from numerous interactions on the surface of the SnO2 nanoparticles. A light-modulated artificial synapse device is realized on a paper at a low voltage bias of -0.01V, with an average recognition rate of 91.7% based on the Yale Face Database. As a security device on a banknote, 400 devices in a 20 × 20 array configuration exhibited random electrical characteristics owing to the local morphology of the SnO2 nanoparticles and differences in the depletion layer width at the SnO2/PVK interface. The security Physically Unclonable Functions (PUF) key based on the current distribution extracted at -1V show unpredictable reproducibility with 50% uniformity, 48.7% inter-Hamming distance, and 50.1% bit-aliasing rates. Moreover, the device maintained its properties for more than 210 days under a curvature radius of 8.75mm and bias and UV irradiation stress conditions.

Characterization of ZnWO4, MgWO4, and CaWO4 Ceramics Synthesized in the Field of a Powerful Radiation Flux

This paper presents the results of a study on the morphology, structure, and luminescent properties of ceramics synthesized in the radiation field of MeWO4 compositions (where Me is Mg, Ca, and Zn). The synthesis of ceramics was carried out by the direct action of the electron flux on an initial mixture of powders of the given stoichiometric composition. WO3, ZnO, MgO, and CaO powders with particle sizes in the range of 1–50 microns were used for the synthesis of the samples. It was found that the yield of the radiation synthesis reaction (the ratio of the mass of the sample and the charge used), when treated with an electron flux with an energy of 1.4 MeV and a flux power density of 15–18 kW/cm2, was in the range of 75–99%. The synthesis of all compositions was carried out under the same radiation treatment modes, although the melting temperatures of the starting materials varied significantly and ranged from 1473 °C (WO3) to 2825 °C (MgO). The study of the ceramic structure showed that under the radiation effect of powerful radiation fluxes on the charge, a crystalline phase of the appropriate composition formed, regardless of the synthesis modes. The results of XRD studies show that during the radiation treatment of the charge, ceramics are formed mainly with the crystalline phases ZnWO4, MgWO4, and CaWO4. These resulting MeWO4 ceramics can be used for the same purposes as crystals. Photoluminescence (PL) and cathodoluminescence (CL) were studied under excitation using stationary ultraviolet radiation and nanosecond pulses of electron flux. In general, the PL and CL of synthesized ceramic samples ZnWO4, MgWO4, and CaWO4 showed that their luminescent properties are similar to those of luminescence in corresponding crystalline materials. This indicates the formation of a crystalline phase in synthesized ceramic samples.

Perspective: towards real-time extreme ultraviolet to x-ray imaging and spectroscopy of laser-driven materials

Abstract Optical manipulation of light is a highly relevant concept in modern solid-state physics and its microscopic mechanisms are widely investigated. From this perspective, we discuss how x-ray and extreme ultraviolet pulses that probe a material during the time it is driven by optical light can deliver valuable microscopic details about electron dynamics.

A flexible beamline combining XUV attosecond pulses with few-femtosecond UV and near-infrared pulses for time-resolved experiments.

We describe a beamline where few-femtosecond ultraviolet (UV) pulses are generated and synchronized to few-cycle near-infrared (NIR) and extreme ultraviolet (XUV) attosecond pulses. The UV light is obtained via third-harmonic generation in argon or neon gas when focusing a phase-stabilized NIR driving field inside a glass cell that was designed to support high pressures for enhanced conversion efficiency. A recirculation system allows reducing the large gas consumption required for the nonlinear process. Isolated attosecond pulses are generated using the polarization gating technique, and the photon spectrometer employed to characterize the XUV radiation consists of a new design based on the combination of a spherical varied-line-space grating and a cylindrical mirror. This design allows for compactness while providing a long entrance arm for integrating different experimental chambers. The entire interferometer is built under vacuum to prevent both absorption of the XUV light and dispersion of the UV pulses, and it is actively stabilized to ensure an attosecond delay stability during experiments. This table-top source has been realized with the aim of investigating UV-induced electron dynamics in neutral states of bio-relevant molecules, but it also offers the possibility to implement a manifold of novel time-resolved experiments based on photo-ionization/excitation of gaseous and liquid targets by ultraviolet radiation. UV pump-XUV probe measurements in ethyl-iodide showcase the capabilities of the attosecond beamline.

Fast spectroscopic imaging using extreme ultraviolet interferometry.

Extreme ultraviolet pulses as generated by high harmonic generation (HHG) are a powerful tool for both time-resolved spectroscopy and coherent diffractive imaging. However, the integration of spectroscopy and microscopy to harness the unique broadband spectra provided by HHG is hardly explored due to the challenge to decouple spectroscopic and microscopic information. Here, we present an interferometric approach to this problem that combines Fourier transform spectroscopy (FTS) with Fourier transform holography (FTH). This is made possible by the generation of phase-locked pulses using a pair of HHG sources. Crucially, in our geometry the number of interferometric measurements required is at most equal to the number of high-harmonics in the illumination, and can be further reduced by incorporating prior knowledge about the structure of the FTH sample. Compared to conventional FTS, this approach achieves over an order of magnitude increase in acquisition speed for full spectro-microscopic data, and furthermore allows high-resolution computational imaging.

Structured illumination microscopy with extreme ultraviolet pulses

Structured illumination microscopy with extreme ultraviolet pulses

All-photonic artificial synapses based on photochromic perovskites for noncontact neuromorphic visual perception

Recently optoelectronic synapses generating light-driven electrical memories have played a vital role in the neuromorphic computing of visual perception. However, all the optoelectronic synapses demonstrate photoelectric conversion. Peripheral circuits are used for contact photocurrent measurement, leading to significant energy consumption and impeding the evolution of optical wireless communication. It is crucial to develop noncontact neuromorphic visual perception based on light-driven photonic memories. Herein, we report all-photonic artificial synapses based on photochromic perovskites. Triggered by ultraviolet and visible light pulses, cesium lead iodide bromine induces a structural disorder. Optical transmittance changes induced by the disorder last after the pulses are gone. Next, the photonic memories are propagated in the air and processed by a recurrent neural network. The accuracy of binary image recognition is instantly stabilized at 1.0, and accuracy above 0.8 after 7 epochs is achieved in the recognition of digitals from 0 to 9. The all-photonic synapses realize remote perception with zero in-situ energy consumption and enable artificial sensory systems with low-power computation, remote control, and ultrahigh propagation speed.

High-density nanodot structures on silicon solar cell surfaces irradiated by ultraviolet laser pulses below the melting threshold fluence

The surface morphology of silicon solar cells irradiated with KrF excimer laser pulses (λ = 248 nm, τ = 20 ns) was investigated below the experimentally observed melting threshold fluence (F th) of 0.47 J cm−2 (±20%). At laser fluences of 0.23–0.48 J cm−2 (equivalent to 0.49F th to 1.0F th), nanodot structures with a height and width of approximately 60–120 nm were periodically formed with an interdot spacing similar to the laser wavelength. The observed nanodot density (29 dots μm2) was higher than that previously obtained at longer wavelengths. Furthermore, crystallinity analysis by micro-Raman spectroscopy revealed a Raman shift of 519.56 cm−1 after irradiation (N= 1500 pulses), compared with 518.27 cm−1 prior to irradiation. A laser fluence of 0.41 J cm−2 ( = 0.87F th) was found to induce compressive stress on the silicon solar cell surface.

UV 30 fs laser pulse generation using a multi-pass cell.

Ultrashort ultraviolet (UV) pulses are pivotal for resolving ultrafast electron dynamics. However, their efficient generation is strongly impeded by material dispersion and two-photon absorption, in particular, if pulse durations around a few tens of femtoseconds or below are targeted. Here, we present a new (to our knowledge) approach to ultrashort UV pulse generation: using the fourth-harmonic generation output of a commercial ytterbium laser system delivering 220 fs UV pulses, we implement a multi-pass cell (MPC) providing 5.6 µJ pulses at 256 nm, compressed to 30.5 fs. Our results set a short-wavelength record for MPC post-compression while offering attractive options to navigate the trade-off between upconversion efficiency and acceptance bandwidth for UV pulse production.

Generation of sub-10-fs deep and extreme ultraviolet pulses for time-resolved photoemission spectroscopy.

We present a light source capable of generating sub-10-fs deep UV (DUV) and extreme UV (EUV) pulses for use in time-resolved photoemission spectroscopy. The fundamental output of a Ti:sapphire laser was compressed using the multi-plate method and mixed with the uncompressed second harmonic in a filamentation four-wave mixing process to generate sub-10-fs DUV pulses. Sub-10-fs EUV pulses were generated via high-order harmonic generation driven by the second harmonic pulses that were compressed using Ar gas and chirped mirrors. The minimum cross correlation time between 267 and 57 nm (corresponding to 21.7 eV) was measured to be 10.6 ± 0.4 fs.

Coherent modulation of intense XUV pulses by ground-state coupling

We present and validate a method to modify the interaction between laser fields and an atomic three-level system based on the control of the ground state, which is interpreted with a direct analytical formula. Coherent modulation of intense extreme Ultraviolet (XUV) pulses is achieved by using near-infrared (NIR) lasers as control pulses interacting with the atomic systems, i.e. quantum transition paths are manipulated in light-matter interactions caused by the laser. We analyze the feasibility of realizing the phase reversal of the dipole response in the three-level system by controlling the interaction between the ground state and another excited state. The discussion of the modulation of intense XUV pulses complements recent studies relying on perturbative excitation. These observations provide new insights for achieving pulse shaping of the XUV frequency range by using the NIR pulse as a control pulse.

Highly flexible liquid metal/photocurable polymer electrodes via direct laser patterning

A highly flexible electrode was fabricated using eutectic gallium-indium (eGaIn) liquid metal combined with an ultraviolet (UV)-curable polyurethane acrylate (PUA) polymer. The eGaIn liquid metal electrodes prepared by a negative-type direct patterning technique using a UV pulse laser can eliminate the need for complex photolithography masks. The optimal UV pulsed laser peak fluence was ∼1.43 J/cm2 to pattern and sinter the eGaIn/PUA composite electrode simultaneously. The laser-patterned eGaIn/PUA composite electrode under the optimal laser condition exhibited a remarkable electrical conductivity of 6.33 × 105 S/m with a patterning resolution of ∼40 μm. Moreover, the resistance of the electrode only deteriorated by 0.95% after 50,000 cycles of severe cyclic folding at a peak strain of 2.5% with a bending radius of 1 mm, demonstrating its exceptional flexibility and durability. These easily patterned eGaIn flexible electrodes via direct laser patterning techniques hold great promise for applications in wearable and flexible electronic devices that require extreme flexibility.

88‐2: The Characteristics Analysis for Laser Cutting Process of Multilayers Display Panels

In this study, we analyzed the laser cutting characteristics of pulse transverse electrical discharge in gas at atmospheric pressure (TEA) CO2 and ultraviolet (UV) pulse laser processing in a multilayer display panels. First, the numerical calculation for was performed to confirm the thermal characteristics of each materials and optical field distribution at the interface of different material layers. Also, processing characteristics were experimentally confirmed by measuring cutting profile and adhesion characteristics of layer interface. Experimental results show that the characteristics of multi layers polymer cutting have different trend from those in a single‐layer because of the optical and thermal properties of each layer. In particular, the interface of layers had a substantial affect due to optical field distributions and thermal characteristic difference. Also, the optical absorbance of layers affect adhesion at the interface. The result suggests proper processing condition to enhance the laser ablation processing quality of multilayer display panel. In conclusion, understanding the characteristics of multilayer laser cutting processing is important for determining the optimal conditions for display panel micromachining and enhancing the quality of laser cutting for the cutting edge technology.