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Kenji Tamasaku

Publications and source records attributed to Kenji Tamasaku.

At least 19 recordsLinked to original sources

Electric-field-induced X-ray Nonreciprocal Dichroism in Hematite

Hematite (alpha-Fe2O3) is a prototypical room temperature antiferromagnet whose time-reversal-odd magnetic structure has recently attracted renewed attention. While such magnetic symmetry can be characterized in terms of higher-order multipoles beyond the magnetic dipole, their manifestation in measurable physical phenomena has remained largely elusive. In this work, we investigate x-ray absorption near the Fe K-edge of hematite under an applied electric field, which explicitly breaks space-inversion symmetry. We observe an electric-field-induced x-ray nonreciprocal linear dichroism (E-induced XNLD) that reflects the time-reversal-odd nature of the magnetic order. Numerical simulations based on ab-initio density functional theory reproduce the observed spectra, including their dependence on the antiferromagnetic domain and x-ray polarization. Furthermore, a symmetry-resolved multipole analysis reveals that this response originates from the magnetic quadrupole and the magnetic toroidal octupole induced by the applied electric field. These results demonstrate that electric-field-modulated x-ray absorption provides direct access to the antiferroic order of higher-order multipoles in time-reversal-odd antiferromagnets, thereby establishing a general framework to uncover hidden symmetry properties in magnetic materials.

cond-mat.mtrl-sci

Soft and hard x-ray orbital-resolved photoemission study of a strongly correlated Cd-Ce quasicrystal approximant

We have investigated the orbital-dependent electronic states of Cd6Ce, a prototype of strongly correlated rare-earth-based Tsai-type quasicrystals and approximants (ACs) by soft and hard x-ray photoemission spectroscopy. Our results reveal that the 4f orbitals are predominantly hybridized with the valence-band electrons far from the Fermi level (EF), in sharp contrast to the hybridization with conduction electrons at EF seen for the intermetallic Ce-based compounds. This anomalous hybridization should be taken into account in discussing the unresolved magnetic ground state in Cd6Ce. These findings suggest that Cd-based ACs, some of which show the multi-step magnetic transitions, could provide a new platform for investigating novel magnetic properties that cannot be understood within the conventional framework of hybridization at EF.

cond-mat.str-el

X-ray-induced quenching of the $^{229}$Th clock isomer in CaF$_2$

Thorium-229 has the lowest nuclear-excited state (an isomer state) at approximately 8.356 eV, making it excitable with tabletop vacuum-ultraviolet lasers. Despite the recent success of laser excitation, the isomer quenching inside the solid-state environment remains unresolved. In this letter, we present experiments investigating X-ray-induced isomer quenching in the CaF$_2$ host, focusing on the effects of X-ray flux and temperature on the lifetime and yield of the isomer state. Our studies reveal a correlation between isomer production, isomer lifetime during irradiation, and post-irradiation afterglow of the target crystal across different temperatures, highlighting a strong relationship between isomer quenching and color-center dynamics. We developed a model to interpret the isomer quenching and the crystal's luminescence.

cond-mat.mtrl-sci

X-ray Phase Measurements by Time-Energy Correlated Photon Pairs

The invention of X-ray interferometers has led to advanced phase-sensing devices that are invaluable in various applications. These include the precise measurement of universal constants, e.g. the Avogadro number, of lattice parameters of perfect crystals, and phase-contrast imaging, which resolves details that standard absorption imaging cannot capture. However, the sensitivity and robustness of conventional X-ray interferometers are constrained by factors, such as fabrication precision, beam quality, and, importantly, noise originating from external sources or the sample itself. In this work, we demonstrate a novel X-ray interferometric method of phase measurement with enhanced immunity to various types of noise, by extending, for the first time, the concept of the SU(1,1) interferometer into the X-ray regime. We use a monolithic silicon perfect crystal device with two thin lamellae to generate correlated photon pairs via spontaneous parametric down-conversion (SPDC). Arrival time coincidence and sum-energy filtration allow a high-precision separation of the correlated photon pairs, which carry the phase information from orders-of-magnitude larger uncorrelated photonic noise. The novel SPDC-based interferometric method presented here is anticipated to exhibit enhanced immunity to vibrations as well as to mechanical and photonic noise, compared to conventional X-ray interferometers. Therefore, this SU(1,1) X-ray interferometer should pave the way to unprecedented precision in phase measurements, with transformative implications for a wide range of applications.

physics.optics

A simple method to find temporal overlap between THz and X-ray pulses using X-ray-induced carrier dynamics in semiconductors

X-ray-induced carrier dynamics in silicon and gallium arsenide were investigated through intensity variations of transmitted terahertz (THz) pulses in the pico to microsecond time scale with X-ray free-electron laser and synchrotron radiation. We observed a steep reduction in THz transmission with a picosecond scale due to the X-ray-induced carrier generation, followed by a recovery on a nano to microsecond scale caused by the recombination of carriers. The rapid response in the former process is applicable to a direct determination of temporal overlap between THz and X-ray pulses for THz pump-X-ray probe experiments with an accuracy of a few picoseconds.

cond-mat.mtrl-sci

Photo-induced phase transition on black samarium monosulfide

To investigate the role of the excitons for the origin of the pressure-induced phase transition (BGT) from the black-colored insulator (BI) to the golden-yellow-colored metal (GM) of samarium monosulfide (SmS), optical reflectivity, Sm $3d$ X-ray absorption spectroscopy (XAS), and X-ray diffraction (XRD) with the creation of excitons by photoexcitation (PE) are reported. In the pump-probe reflectivity measurement, following a huge reflectivity change of about 22 %, three different relaxation times with a vibration component were observed. The fast component with the relaxation time ($\tau$) of less than 1 ps is due to the excitation and relaxation of electrons into the conduction band, and the slowest one with $\tau > {\rm several} 100$ ps originates from the appearance of the photo-induced (PI) state. The components with $\tau \sim 10$ ps and vibration originate from the appearance of the PI state and the interference between the reflection lights at the sample surface and the boundary between the BI and PI states, suggesting that the electronic structure of the PI phase is different from that of the BI state. XAS spectra indicate that the Sm mean valence is shifted from the Sm$^{2+}$ dominant to the intermediate between Sm$^{2+}$ and Sm$^{3+}$ by PE but did not change to that of the GM phase across BGT, consistent with the reflectivity data. The XRD result after PE shows that the PI state has much less lattice contraction than the GM phase. These results suggest that the BGT cannot be achieved solely by creating excitons after PE but requires other effects, such as a lattice contraction.

cond-mat.str-el

Controlling $^{229}$Th isomeric state population in a VUV transparent crystal

The radioisotope Th-229 is renowned for its extraordinarily low-energy, long-lived nuclear first-excited state. This isomeric state can be excited by VUV lasers and the transition from the ground state has been proposed as a reference transition for ultra-precise nuclear clocks. Such nuclear clocks will find multiple applications, ranging from fundamental physics studies to practical implementations. Recent investigations extracted valuable constraints on the nuclear transition energy and lifetime, populating the isomer in stochastic nuclear decay of U-233 or Ac-229. However, to assess the feasibility and performance of the (solid-state) nuclear clock concept, time-controlled excitation and depopulation of the $^{229}$Th isomer together with time-resolved monitoring of the radiative decay are imperative. Here we report the population of the $^{229}$Th isomeric state through resonant X-ray pumping and detection of the radiative decay in a VUV transparent $^{229}$Th-doped CaF$_2$ crystal. The decay half-life is measured to $447\pm 25$ s, with a transition wavelength of $148.18 \pm 0.42$ nm and a radiative decay fraction consistent with unity. Furthermore, we report a new ``X-ray quenching'' effect which allows to de-populate the isomer on demand and effectively reduce the half-life by at least a factor 50. Such controlled quenching can be used to significantly speed up the interrogation cycle in future nuclear clock schemes. Our results show that full control over the $^{229}$Th nuclear isomer population can be achieved in a crystal environment. In particular, non-radiative decay processes that might lead to a broadening of the isomer transition linewidth are negligible, paving the way for the development of a compact and robust solid-state nuclear clock. Further studies are needed to reveal the underlying physical mechanism of the X-ray quenching effect.

nucl-ex

Non-equilibrium pathways to emergent polar supertextures

Ultrafast stimuli can stabilize metastable states of matter inaccessible by equilibrium means. Establishing the spatiotemporal link between ultrafast excitation and metastability is crucial to understanding these phenomena. Here, we use single-shot optical-pump, X-ray-probe measurements to provide snapshots of the emergence of a persistent polar vortex supercrystal in a heterostructure that hosts a fine balance between built-in electrostatic and elastic frustrations by design. By perturbing this balance with photoinduced charges, a starting heterogenous mixture of polar phases disorders within a few picoseconds, resulting in a soup state composed of disordered ferroelectric and suppressed vortex orders. On the pico-to-nanosecond timescales, transient labyrinthine fluctuations form in this soup along with a recovering vortex order. On longer timescales, these fluctuations are progressively quenched by dynamical strain modulations, which drive the collective emergence of a single supercrystal phase. Our results, corroborated by dynamical phase-field modeling, reveal how ultrafast excitation of designer systems generates pathways for persistent metastability.

cond-mat.mtrl-sci

Ultrafast Control of Crystal Structure in a Topological Charge-Density-Wave Material

Optical control of crystal structures is a promising route to change physical properties including topological nature of a targeting material. Time-resolved X-ray diffraction measurements using the X-ray free-electron laser are performed to study the ultrafast lattice dynamics of VTe$_2$, which shows a unique charge-density-wave (CDW) ordering coupled to the topological surface states as a first-order phase transition. A significant oscillation of the CDW amplitude mode is observed at a superlattice reflection as well as Bragg reflections. The frequency of the oscillation is independent of the fluence of the pumping laser, which is prominent to the CDW ordering of the first-order phase transition. Furthermore, the timescale of the photoinduced 1$T^{\prime\prime}$ to 1$T$ phase transition is independent of the period of the CDW amplitude mode.

cond-mat.str-el

Observation of a Critical Charge Mode in a Strange Metal

Quantum electronic matter has long been understood in terms of two limiting behaviors of electrons: one of delocalized metallic states, and the other of localized magnetic states. Understanding the strange metallic behavior which develops at the brink of localization demands new probes of the underlying electronic charge dynamics. Using a state-of-the-art technique, synchrotron-radiation-based Mossbauer spectroscopy, we have studied the longitudinal charge fluctuations of the strange metal phase of beta-YbAlB4 as a function of temperature and pressure. We find that the usual single absorption peak in the Fermi-liquid regime splits into two peaks upon entering the critical regime. This spectrum is naturally interpreted as a single nuclear transition, modulated by nearby electronic valence fluctuations whose long time-scales are further enhanced, due to the formation of charged polarons. Our results represent a direct observation of critical charge fluctuations as a new signature of strange metals.

cond-mat.str-el

Shortening X-ray Pulse Duration via Saturable Absorption

To shorten the duration of x-ray pulses, we present a nonlinear optical technique using atoms with core-hole vacancies (core-hole atoms) generated by inner-shell photoionization. The weak Coulomb screening in the core-hole atoms results in decreased absorption at photon energies immediately above the absorption edge. By employing this phenomenon, referred to as saturable absorption, we successfully reduce the duration of x-ray free-electron laser pulses (photon energy: 9.000 keV, duration: 6-7 fs, fluence: 2.0-3.5$\times$10$^5$ J/cm$^2$) by $\sim$35%. This finding that core-hole atoms are applicable to nonlinear x-ray optics is an essential stepping stone for extending nonlinear technologies commonplace at optical wavelengths to the hard x-ray region.

physics.optics

Absolute X-ray energy measurement using a high-accuracy angle encoder

This paper presents an absolute X-ray photon energy measurement method that uses a Bond diffractometer. The proposed system enables the prompt and rapid in-situ measurement of photon energies in a wide energy range. The diffractometer uses a reference silicon single crystal plate and a highly accurate angle encoder called SelfA. We evaluate the performance of the system by repeatedly measuring the energy of the first excited state of the potassium-40 nuclide. The excitation energy is determined as 29829.39(6) eV. It is one order of magnitude more precise than the previous measurement. The estimated uncertainty of the photon energy measurement was 0.7 ppm as a standard deviation and the maximum observed deviation was 2 ppm.

physics.ins-det

Nonlinear resonant X-ray Raman scattering

We report the observation of a novel nonlinear effect in the hard x-ray range. Upon illuminating Fe and Cu metal foils with intense x-ray pulses tuned near their respective K edges, photons at nearly twice the incoming photon energy are emitted. The signal rises quadratically with the incoming intensity, consistent with two-photon excitation. The spectrum of emitted high-energy photons comprises multiple Raman lines that disperse with the incident photon energy. Upon reaching the double K-shell ionization threshold, the signal strength undergoes a marked rise. Above this threshold, the lines cease dispersing, turning into orescence lines with energies much greater than obtainable by single electron transitions, and additional Raman lines appear. We attribute these processes to electron-correlation mediated multielectron transitions involving double-core hole excitation and various two-electron de-excitation processes to a final state involving one or more L and M core-holes.

physics.atom-ph

Transient quantum isolation and critical behavior in the magnetization dynamics of half-metallic manganites

We combine time resolved pump-probe Magneto-Optical Kerr Effect and Photoelectron Spectroscopy experiments supported by theoretical analysis to determine the relaxation dynamics of delocalized electrons in half-metallic ferromagnetic manganite $La_{1-x}Sr_{x}MnO_{3}$. We observe that the half-metallic character of $La_{1-x}Sr_{x}MnO_{3}$ determines the timescale of both the electronic phase transition and the quenching of magnetization, revealing a quantum isolation of the spin system in double exchange ferromagnets extending up to hundreds of picoseconds. We demonstrate the use of time-resolved hard X-ray photoelectron spectroscopy (TR-HAXPES) as a unique tool to single out the evolution of strongly correlated electronic states across a second-order phase transition in a complex material.

cond-mat.str-el

Scientific Opportunities with an X-ray Free-Electron Laser Oscillator

An X-ray free-electron laser oscillator (XFELO) is a new type of hard X-ray source that would produce fully coherent pulses with meV bandwidth and stable intensity. The XFELO complements existing sources based on self-amplified spontaneous emission (SASE) from high-gain X-ray free-electron lasers (XFEL) that produce ultra-short pulses with broad-band chaotic spectra. This report is based on discussions of scientific opportunities enabled by an XFELO during a workshop held at SLAC on June 29 - July 1, 2016

physics.ins-det

X-ray pumping of the Th-229 nuclear clock isomer

Thorium-229 is a unique case in nuclear physics: it presents a metastable first excited state Th-229m, just a few electronvolts above the nuclear ground state. This so-called isomer is accessible by VUV lasers, which allows transferring the amazing precision of atomic laser spectroscopy to nuclear physics. Being able to manipulate the Th-229 nuclear states at will opens up a multitude of prospects, from studies of the fundamental interactions in physics to applications as a compact and robust nuclear clock. However, direct optical excitation of the isomer or its radiative decay back to the ground state has not yet been observed, and a series of key nuclear structure parameters such as the exact energies and half-lives of the low-lying nuclear levels of Th-229 are yet unknown. Here we present the first active optical pumping into Th-229m. Our scheme employs narrow-band 29 keV synchrotron radiation to resonantly excite the second excited state, which then predominantly decays into the isomer. We determine the resonance energy with 0.07 eV accuracy, measure a half-life of 82.2 ps, an excitation linewidth of 1.70 neV, and extract the branching ratio of the second excited state into the ground and isomeric state respectively. These measurements allow us to re-evaluate gamma spectroscopy data that have been collected over 40~years.

nucl-ex

Effect of Anisotropic Hybridization in YbAlB$_4$ Probed by Linear Dichroism in Core-Level Hard X-ray Photoemission Spectroscopy

We have probed the crystalline electric-field ground states of pure $|J = 7/2, J_z = \pm 5/2\rangle$ as well as the anisotropic $c$-$f$ hybridization in both valence fluctuating systems $α$- and $β$-YbAlB$_4$ by linear polarization dependence of angle-resolved core level photoemission spectroscopy. Interestingly, the small but distinct difference between \abyb was found in the polar angle dependence of linear dichroism, indicating the difference in the anisotropy of $c$-$f$ hybridization which may be essential to a heavy Fermi liquid state in $α$-YbAlB$_4$ and a quantum critical state in $β$-YbAlB$_4$.

cond-mat.str-el

Ultrafast demagnetization of Pt magnetic moment in L1${}_0$-FePt probed by hard x-ray free electron laser

We demonstrate ultrafast magnetization dynamics in a 5d transition metal using circularly-polarized x-ray free electron laser in the hard x-ray region. A decay time of light-induced demagnetization of L1${}_0$-FePt was determined to be $τ_\textrm{Pt} = 0.6\ \textrm{ps}$ using time-resolved x-ray magnetic circular dichroism at the Pt L${}_3$ edge, whereas magneto-optical Kerr measurements indicated the decay time for total magnetization as $τ_\textrm{total} = 0.1\ \textrm{ps}$. A transient magnetic state with the photo-modulated magnetic coupling between the 3d and 5d elements is firstly demonstrated.

cond-mat.mtrl-sci