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The single-line-of-sight time-resolved x-ray imager (SLOS-TRXI), a fast-gated x-ray imager used for capturing x-ray self-emission in inertial confinement fusion experiments on OMEGA, has been upgraded and characterized. SLOS-TRXI combines an electron-dilation imager and a hybrid complementary metal–oxide–semiconductor (hCMOS) sensor to capture multiple gated frames on a single line of sight with a temporal resolution of ∼40 ps and a spatial resolution of 10 µm. The original hCMOS sensor with four frames was replaced with a newer-generation hCMOS sensor having eight frames. Gate characterizations of both the sensor and the entire SLOS-TRXI diagnostic were performed using ∼10-ps FWHM visible (2ω) and UV (4ω) short-pulse lasers, respectively. A stepped echelon was used to generate a train of five UV laser pulses having an interpulse separation of 30 ± 3 ps. Characterization results of the hCMOS gating (2.28 ± 0.02-ns FWHM on average) and a temporal resolution of the upgraded SLOS-TRXI (34 ± 4-ps FWHM on average) are presented. A temporal magnification for the electron-dilation imager between 40 and 60 was inferred from the characterization results. The spatial resolution of the upgraded SLOS-TRXI remains the same in light of this work. [ABSTRACT FROM AUTHOR]

A long gas cell, filled with noble gas, is typically positioned between the undulator and the first mirror in the free-electron laser (FEL) beamline to attenuate the laser power as required by the end-stations. In addition to attenuation, the gas cell also serves important functions in various applications, such as spectrometer calibration, resolving power evaluation during beamline commissioning, and filtering of third harmonic in FEL operations. These functions of the gas cell have been successfully tested and implemented at the Dalian Coherent Light Source, a vacuum ultraviolet FEL facility located in Dalian, China. The resolving power of higher than 5000 has been obtained, and accurate calibration has been completed using the gas cell. During operation, the third harmonic of the FEL was attenuated by approximately one order of magnitude with almost the same power of the fundamental. This greatly improved the signal-to-noise ratio at the end-stations. [ABSTRACT FROM AUTHOR]

We present a detailed exposition of the design for time- and angle-resolved photoemission spectroscopy using a UV probe laser source that combines the nonlinear effects of β-BaB2O4 and KBe2BO3F2 optical crystals. The photon energy of the probe laser can be switched between 6.0 and 7.2 eV, with the flexibility to operate each photon energy setting under two distinct resolution configurations. Under the fully optimized energy resolution configuration, we achieve an energy resolution of 8.5 meV at 6.0 eV and 10 meV at 7.2 eV. Alternatively, switching to the other configuration enhances the temporal resolution, yielding a temporal resolution of 72 fs for 6.0 eV and 185 fs for 7.2 eV. We validated the performance and reliability of our system by applying it to measuring two typical materials: the topological insulator MnBi2Te4 and the excitonic insulator candidate Ta2NiSe5. [ABSTRACT FROM AUTHOR]

A newly developed instrument comprising a near ambient pressure (NAP) photoemission electron microscope (PEEM) and a tunable deep ultraviolet (DUV) laser source is described. This NAP-PEEM instrument enables dynamic imaging of solid surfaces in gases at pressures up to 1 mbar. A diode laser (976 nm) can illuminate a sample from the backside for in situ heating in gases up to 1200 K in minutes. The DUV laser with a tunable wavelength between 175 nm and 210 nm is perpendicularly incident onto the sample surface for PEEM imaging of a wide spectrum of solids with different surface work functions. Using this setup, we have first demonstrated spatiotemporal oscillation patterns of CO oxidation reaction on Pt(110) from high vacuum to NAPs and gas-induced restructuring of metal nanostructures in millibar gases. The new facility promises important applications in heterogeneous catalysis, electrochemical devices, and other surface processes under nearly working conditions. [ABSTRACT FROM AUTHOR]

A method of ultraviolet germicidal irradiation (UVGI) for water pathogen inactivation effectiveness using tunable, narrowband laser light is described. A transportable tunable UV (TTUV) laser system for providing a known irradiance (μW/cm2) or dose (mJ/cm2) suitable for irradiating water samples in Petri dishes over the wavelength range of 210 nm–300 nm was developed by the National Institute of Standards and Technology. The TTUV facility, consisting of a 1 kHz pulsed UV laser and light-tight enclosure containing the optics necessary to uniformly irradiate a water sample, was used in a microbiology laboratory to dose drinking water pathogens and surrogates as part of a Water Research Foundation study in the summer and fall of 2012. The approach demonstrated improved accuracy and simplified spectral analysis over conventional pathogen inactivation sources consisting of broadband UV sources and bandpass filters. In this work, the TTUV facility design and key components are described, including modifications in the field to provide the required irradiance levels. The irradiance and dose levels produced by the tunable UV laser during the project are also presented. The transportability of the TTUV system enabled it to be brought to a microbiology facility allowing the water samples (microbial suspensions) to be irradiated in a location with experienced staff and facilities for preparing, handling, analyzing, storing, and shipping the many samples studied. These results, published elsewhere, established that the tunable UV laser system provides unique UVGI capabilities for use with water pathogens and has applications for other pathogen experiments, for example, air-purification studies. [ABSTRACT FROM AUTHOR]

Performing time- and angle-resolved photoemission (tr-ARPES) spectroscopy at high momenta necessitates extreme ultraviolet laser pulses, which are typically produced via high harmonic generation (HHG). Despite recent advances, HHG-based setups still require large pulse energies (from hundreds of μJ to mJ) and their energy resolution is limited to tens of meV. Here, we present a novel 11 eV tr-ARPES setup that generates a flux of 5 × 1010 photons/s and achieves an unprecedented energy resolution of 16 meV. It can be operated at high repetition rates (up to 250 kHz) while using input pulse energies down to 3 µJ. We demonstrate these unique capabilities by simultaneously capturing the energy and momentum resolved dynamics in two well-separated momentum space regions of a charge density wave material ErTe3. This novel setup offers the opportunity to study the non-equilibrium band structure of solids with exceptional energy and time resolutions at high repetition rates. [ABSTRACT FROM AUTHOR]

This paper describes an experimental technique for studying neutral metal complexes using infrared + vacuum ultraviolet (IR+VUV) two-color ionization spectroscopy based on a tunable VUV free-electron laser (VUV-FEL). The preliminary IR spectroscopy results of mass-selected nickel tetracarbonyl are reported in this work. The results demonstrate that the tunable VUV-FEL light allows the selective ionization of a given neutral cluster free of confinement along with the recording of well-resolved IR spectra. As the ionization energies of many neutral clusters are accessible by a broadly tunable VUV-FEL (50–150 nm) and near-threshold ionization can be readily achieved, the proposed experimental method offers unique possibilities for the size-specific study of a wide variety of confinement-free neutral clusters. [ABSTRACT FROM AUTHOR]

A method was developed with laser-irradiated Au planar foils to characterize the focal spot of UV laser beams on a target at full energy from soft x-ray emission. A pinhole camera with a back-thinned charge-coupled device detector and filtration with thin Be and Al foil filters provides images of the x-ray emission at photon energies <2 keV. This method requires a careful measurement of the relationship between the applied UV fluence and the x-ray signal, which can be described by a power-law dependence. The measured exponent γ ∼ 2 provides a dynamic range of ∼25 for the inferred UV fluence. UV fluence profiles of selected beams were measured for 100-ps and 1-ns laser pulses and were compared to directly measured profiles from an UV equivalent-target-plane diagnostic. The inferred spot size and super-Gaussian order from the x-ray technique agree within several percent with the values measured with the direct UV measurements. [ABSTRACT FROM AUTHOR]

We have developed an integrated instrument combining deep ultraviolet laser ionization mass spectrometry (DUV-LIMS) and infrared multiphoton dissociation (IR-MPD) spectroscopy, abbreviated as DUV-IR. The 177.3 nm DUV laser (7 eV single-photon energy) has short pulse duration (15 ps) and appropriate pulse energy (∼20 µJ), which is found to be highly efficient for low-fragment photoionization of neutral metal clusters and molecules. A home-made cluster source is designed with an adjustable formation channel suitable for the generation of different cluster series. The well-aligned components of the reflection time-of-flight mass spectrometer, as well as the coaxial design of DUV laser and molecular beam, bring forth high sensitivity and high resolution of the DUV-LIMS. Taking these advantages, well-resolved neutral Vn (n = 1–43) and (Benzene)n (n = 1–25) clusters have been generated free of fragmentation. In addition to the generation and detection of neutral clusters, a fast-flow reaction tube is also designed downstream of the cluster source allowing to study their reactivity. In particular, a broad-range tunable IR laser (1.3–16 µm) is coupled with the DUV laser to attain IR-MPD spectroscopic analysis. This integrated system offers a general protocol to prepare various clusters to study their gas-phase reactivity and to determine their structures. [ABSTRACT FROM AUTHOR]

The Dynamic Compression Sector (DCS) laser is a 100-J ultraviolet Nd:glass system designed and built by the Laboratory for Laser Energetics for experimental research at the DCS located at the Advanced Photon Source (Argonne National Laboratory). Its purpose is to serve as a shock driver to study materials under extreme dynamic pressures. It was designed to deposit energy within a uniformly illuminated 500-μm spot on target, with additional optics provided to implement spot sizes of 250 and 1000 μm. Designed after larger-scale glass lasers such as OMEGA and the National Ignition Facility, the laser consists of a fiber front end with interferometer-based pulse shaping, a Nd:glass regenerative amplifier, a four-pass rod amplifier, and a 15-cm glass disk amplifier, through which six passes are made in a bowtie geometry. The output is frequency tripled from 1053 to 351 nm by using a pair of type-II phase-matched KDP crystals, with a third to increase conversion bandwidth. The super-Gaussian spot in the far field is achieved with a distributed phase plate and a 1-m aspherical focusing lens. Beam smoothing is achieved by smoothing by spectral dispersion and polarization smoothing, resulting in a root-mean-square variation in intensity on target of ±8.7%. [ABSTRACT FROM AUTHOR]

We present studies on monoisotopic Hg+ ions generation and trapping at room temperature. An ultraviolet laser system, including a frequency-controlled 194 nm laser and a 254 nm laser, is constructed. Mercury atoms are isotope-selectively excited by the 254 nm laser. The spectrum of the 6s2–6s6p transition lines for natural mercury isotopes is measured, and the uncertainty is less than 100 MHz. Then, the selected mercury isotopes are ionized by the 194 nm laser and trapped in a linear Paul trap. The fluorescence of the ion crystal at 194 nm is detected, and the temperature of the ions is estimated to be less than 10 mK. [ABSTRACT FROM AUTHOR]

In order to supplement manufacturers’ information, this Department will welcome the submission by our readers of brief communications reporting measurements on the physical properties of materials which supersede earlier data or suggest new research applications. [ABSTRACT FROM AUTHOR]

Mass spectrometry imaging (MSI) has important applications in material research, biology, and medicine. The MSI method based on UV laser desorption/ionization (UVLDI) can obtain images of intact samples, but has a high level of molecular fragmentation. In this work, we report a new MSI instrument that uses a VUV laser (125.3 nm) as a desorption/ionization source to exploit its advantages of high single photon energy and small focus size. The new instrument was tested by the mass spectra of Nile red and FGB (Fibrinogen beta chain) samples and mass spectrometric images of a fly brain section. For the tested samples, the VUVDI method offers lower levels of molecular fragmentations and higher sensitivities than those of the UVLDI method and second ion mass spectrometry imaging method using a Bi3+ beam. The ablation crater produced by the focused VUV laser on a quartz plate has an area of 10 μm2. The VUV laser is prepared based on the four-wave mixing method using three collimated laser beams and a heated Hg cell. [ABSTRACT FROM AUTHOR]

To realize an ultraviolet laser with high beam quality and high output power, we are developing a master oscillator power amplifier system for a longitudinally excited gas laser. In this system, high beam quality is produced by an oscillator stage, and high output power is produced by an amplifier stage. Here, the beam profile of the longitudinally excited gas N2 laser had a quasi-Gaussian shape when using a large-diameter discharge tube, which enabled the use of the amplifier stage. The discharge tube consisted of a dielectric pipe with an inner diameter of 14 mm and a length of 30 cm. The discharge tube was covered with a metallic tube for pre-ionization. The strength and spatial distribution of pre-ionization were optimized by adjusting the gap between the metallic tube and the discharge tube. The uniform discharge achieved by controlling the pre-ionization produced a quasi-Gaussian laser beam profile with a correlation factor of 0.99513, a laser pulse energy of 343 μJ, and an input energy of 2.95 J. [ABSTRACT FROM AUTHOR]

A non-destructive diagnostic method for the characterization of circularly polarized, ultraintense, short wavelength free-electron laser (FEL) light is presented. The recently installed Delta undulator at the LCLS (Linac Coherent Light Source) at SLAC National Accelerator Laboratory (USA) was used as showcase for this diagnostic scheme. By applying a combined two-color, multi-photon experiment with polarization control, the degree of circular polarization of the Delta undulator has been determined. Towards this goal, an oriented electronic state in the continuum was created by non-resonant ionization of the O2 1s core shell with circularly polarized FEL pulses at hν ≃ 700 eV. An also circularly polarized, highly intense UV laser pulse with hν ≃ 3.1 eV was temporally and spatially overlapped, causing the photoelectrons to redistribute into so-called sidebands that are energetically separated by the photon energy of the UV laser. By determining the circular dichroism of these redistributed electrons using angle resolving electron spectroscopy and modeling the results with the strong-field approximation, this scheme allows to unambiguously determine the absolute degree of circular polarization of any pulsed, ultraintense XUV or X-ray laser source. [ABSTRACT FROM AUTHOR]

Simultaneous laser locking of infrared (IR) and ultraviolet lasers to a visible stabilized reference laser is demonstrated via a Fabry-Perot (FP) cavity. LabVIEW is used to analyze the input, and an internal proportional-integral-derivative algorithm converts the FP signal to an analog locking feedback signal. The locking program stabilized both lasers to a long term stability of better than 9 MHz, with a custom-built IR laser undergoing significant improvement in frequency stabilization. The results of this study demonstrate the viability of a simple, computer-controlled, non-temperature-stabilized FP locking scheme for our applications, laser cooling of Ca+ ions, and its use in other applications with similar modest frequency stabilization requirements. [ABSTRACT FROM AUTHOR]

A timing system is demonstrated for the OMEGA Laser System that guarantees all 60 beams will arrive on target simultaneously with a root mean square variability of 4 ps. The system relies on placing a scattering sphere at the target position to couple the ultraviolet light from each beam into a single photodetector. [ABSTRACT FROM AUTHOR]

We developed a table-top vacuum ultraviolet (VUV) laser with 113 778 nm wavelength (10.897 eV) . and demonstrated its viability as a photon source for high resolution angle-resolved photoemission spectroscopy (ARPES). This sub-nanosecond pulsed VUV laser operates at a repetition rate of 10 MHz, provides a flux of 2 x 1012 photons/s, and enables photoemission with energy and momentum resolutions better than 2 meV and 0.012 Å-1, respectively. Space-charge induced energy shifts and spectral broadenings can be reduced below 2 meV. The setup reaches electron momenta up to 1.2 Å11, granting full access to the first Brillouin zone of most materials. Control over the linear polarization, repetition rate, and photon flux of the VUV source facilitates ARPES investigations of a broad range of quantum materials, bridging the application gap between contemporary low energy laser-based ARPES and synchrotron-based ARPES. We describe the principles and operational characteristics of this source and showcase its performance for rare earth metal tritellurides, high temperature cuprate superconductors, and iron-based superconductors. [ABSTRACT FROM AUTHOR]

We report on the development and characterization of continuous, narrow-band, and tunable laser systems that use direct second-harmonic generation from blue and green diode lasers with an output power level of up to 11.1 mW in the mid-ultraviolet. One of our laser systems was tuned to the mercury 6¹S0 → 6³P1 intercombination line at 253.7 nm. We could perform Doppler-free saturation spectroscopy on this line and were able to lock our laser to the transition frequency on long time scales. [ABSTRACT FROM AUTHOR]

We report the first experiments carried out on a new chemical and magnetic imaging system, which combines the high spatial resolution of a photoemission electron microscope (PEEM) with a continuous-wave deep-ultraviolet laser. Threshold photoemission is sensitive to the chemical and magnetic structures of the surface of materials. The spatial resolution of PEEM is limited by space charging when using pulsed photon sources as well as aberrations in the electron optics. We show that the use of a continuous-wave laser enabled us to overcome such a limit by suppressing the space-charge effect, allowing us to obtain a resolution of approximately 2.6 nm. With this system, we demonstrated the imaging of surface reconstruction domains on Si(001) by linear dichroism with normal incidence of the laser beam. We also succeeded in magnetic imaging of thin films with the use of magnetic circular dichroism near the Fermi level. The unique features of the ultraviolet laser will give us fast switching of the incident angles and polarizations of the photon source, which will be useful for the characterization of antiferromagnetic materials as well as ferromagnetic materials. [ABSTRACT FROM AUTHOR]

We generate high-order harmonics at high pulse repetition rates using a turnkey laser. High-order harmonics at 400 kHz are observed when argon is used as target gas. In neon, we achieve generation of photons with energies exceeding 90 eV (~13 nm) at 20 kHz. We measure a photon flux of up to 4.4 x 1010 photons per second per harmonic in argon at 100 kHz. Many experiments employing high-order harmonics would benefit from higher repetition rates, and the user-friendly operation opens up for applications of coherent extreme ultra-violet pulses in new research areas. [ABSTRACT FROM AUTHOR]

We have developed an angle-resolved photoemission spectrometer with tunable vacuum ultraviolet laser as a photon source. The photon source is based on the fourth harmonic generation of a near IR beam from a Ti:sapphire laser pumped by a CW green laser and tunable between 5.3 eV and 7 eV. The most important part of the set-up is a compact, vacuum enclosed fourth harmonic generator based on potassium beryllium fluoroborate crystals, grown hydrothermally in the US. This source can deliver a photon flux of over 1014 photon/s. We demonstrate that this energy range is sufficient to measure the kz dispersion in an iron arsenic high temperature superconductor, which was previously only possible at synchrotron facilities. [ABSTRACT FROM AUTHOR]