arXiv subjects

Takahiko Masuda

Publications and source records attributed to Takahiko Masuda.

17 recordsLinked to original sources

arXiv2026

A cryogenic buffer gas beam source with in-situ ablation target replacement

The design and performance of a cryogenic buffer gas beam (CBGB) source with a load-lock system is presented. The ACME III electron electric dipole moment (eEDM) search experiment uses this source to produce a beam of cold, slow thorium monoxide (ThO) molecules. A key feature of the apparatus is its capability to replace ablation targets without interrupting vacuum or cryogenic conditions, increasing the average signal in the eEDM search. The source produces approximately $1.3 \times 10^{11}$ ground-state ThO molecules per pulse, with a rotational temperature of $4.8$ K, molecular beam solid angle of $0.31$ sr, and forward velocity of $200$ m/s. These parameters match the performance of traditional sources that require time-consuming thermal cycles for target replacement. A long-term yield improvement of about 40% is achieved when the load-lock system is used to replace targets biweekly.

physics.atom-ph↗

arXiv2025

Analytical study of birefringent cavities for axion-like dark matter search

Light polarization plays a crucial role in optical-cavity experiments; however, mirror birefringence presents a significant challenge that must be addressed carefully. In this study, a rigorous, nonperturbative framework is developed to quantify birefringence effects by incorporating variations in reflectance and polarization misalignment. We analyze the impact of this framework on the sensitivity of axion-like particle (ALP) dark-matter searches. The results show that both birefringence and misalignment contribute to sensitivity degradation in the low-mass regime; however, the adverse effects of misalignment can be mitigated by selecting a postselection angle greater than the misalignment angle. Furthermore, birefringence produces an additional resonance peak in the high-mass region, which remains largely unaffected by misalignment and postselection variations. This rigorous framework underscores the importance of considering birefringence in high-precision optical-cavity experiments for ALP detection.

hep-ph↗

arXiv2025

Laser Mössbauer spectroscopy of ^{229}Th

Mössbauer spectroscopy is widely used in biochemistry, geology, and solid-state physics to obtain structural information on materials. Here, we extend this technique into the optical range using a vacuum ultraviolet laser to probe the low-energy nuclear transitions of thorium-229, doped in calcium fluoride crystals. We discover four distinct doping sites for the thorium ions, determine the characteristic electric field gradients emerging in the interaction with the host crystal, and identify the microscopic structure of the two dominant configurations. Site-selective laser excitation allows to study the isomeric state lifetime and laser-induced quenching for all sites. This laser-based Mössbauer spectroscopy provides a powerful probe of the nuclear environment, yielding foundational data for designing future solid-state nuclear clocks.

nucl-ex↗

arXiv2025

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↗

arXiv2025

A method to detect the VUV photons from cooled $^{229}$Th:CaF$_2$ crystals

Thorium-229, with its exceptionally low-energy nuclear excited state, is a key candidate for developing nuclear clocks. $^{229}$Th-doped CaF$_2$ crystals, benefiting from calcium fluoride's wide band gap, show great promise as solid-state nuclear clock materials. These crystals are excited by vacuum ultraviolet (VUV) lasers, which over time cause radiation damage. Cooling the crystals can mitigate this damage but introduces a challenge: photoabsorption. This occurs when residual gas molecules condense on the crystal surface, absorbing VUV photons and deteriorating detection efficiency. To solve this, we developed a cooling technique using a copper shield to surround the crystal, acting as a cold trap. This prevents ice-layer formation, even at temperatures below $-100\,^\circ$C, preserving high VUV photon detection efficiency. Our study detailed the experimental cooling setup and demonstrated the effectiveness of the copper shield in maintaining crystal performance, a critical improvement for future solid-state nuclear clocks operating at cryogenic temperatures.

physics.ins-det↗

arXiv2024

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↗

arXiv2022

High-sensitivity low-noise photodetector using large-area silicon photomultiplier

The application of silicon photomultiplier (SiPM) technology for weak-light detection at a single photon level has expanded thanks to its better photon detection efficiency in comparison to a conventional photomultiplier tube (PMT). SiPMs with large detection area have recently become commercially available, enabling applications where the photon flux is low both temporarily and spatially. On the other hand, several drawbacks exist in the usage of SiPMs such as a higher dark count rate, many readout channels, slow response time, and optical crosstalk; therefore, users need to carefully consider the trade-offs. This work presents a SiPM-embedded compact large-area photon detection module. Various techniques are adopted to overcome the disadvantages of SiPMs so that it can be generally utilized as an upgrade from a PMT. A simple cooling component and recently developed optical crosstalk suppression method are adopted to reduce the noise which is more serious for larger-area SiPMs. A dedicated readout circuit increases the response frequency and reduces the number of readout channels. We favorably compare this design with a conventional PMT and obtain both higher photon detection efficiency and larger-area acceptance.

physics.ins-det↗

arXiv2021

Suppression of the optical crosstalk in a multi-channel silicon photomultiplier array

We propose and study a method of optical crosstalk suppression for silicon photomultipliers (SiPMs) using optical filters. We demonstrate that attaching absorptive visible bandpass filters to the SiPM can substantially reduce the optical crosstalk. Measurements suggest that the absorption of near infrared light is important to achieve this suppression. The proposed technique can be easily applied to suppress the optical crosstalk in SiPMs in cases where filtering near infrared light is compatible with the application.

physics.ins-det↗

arXiv2020

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↗

arXiv2019

Development of a measurement system enabling the reconstruction of gamma-ray time spectra by simultaneous recording of energy and time information

We developed a measurement system that enables the reconstruction of γ-ray time spectra in cascade decay schemes. As this system records all the time and energy information of γ-rays, reconstruction is possible after the measurement. Therefore, the energy regions for the γ-ray identification can be optimized in complicated cascade decay schemes. Moreover, in this system we can record data with time-dependent parameters of external perturbations, such as applied magnetic fields, and consequently we can investigate the correlations and responses of γ-rays to the perturbation. This property fulfills the demands required for quantum information research with γ-rays.

physics.ins-det↗

arXiv2019

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↗

arXiv2019

Coherent two-photon emission from hydrogen molecules excited by counter-propagating laser pulses

We observed two-photon emission signals from the first vibrationally excited state of parahydrogen gas excited coherently by counter-propagating laser pulses. A single narrow-linewidth laser source was used to excite the parahydrogen molecules and induce the two-photon emission process. We measured how the signal energy depended on the detuning, target gas pressure, and input pulse energies. These results are qualitatively consistent with those obtained by numerical simulations based on the Maxwell-Bloch equations with one spatial dimension and one temporal dimension. This study of two-photon emission with counter-propagating injection is an important step toward neutrino mass spectroscopy.

physics.atom-ph↗

arXiv2018

Geometry-dependent spectra and coherent-transient measurement of nearly degenerate four-wave mixing using two-photon resonance

We study nearly degenerate four-wave mixing using a two-photon-allowed vibrational transition of parahydrogen. A signal photon is generated by a trigger photon and coherence among parahydrogen, which is prepared by two counterpropagating pump pulses. The dependence of the signal pulse energy on the trigger frequency are investigated. The measured spectra vary depending on the geometry. They shift depending on the direction of the signal pulse and on the small angle formed by the counterpropagating pump pulses. Furthermore, the dependence of signal pulse energy on the incident time of the trigger pulse is investigated. The measured signal pulse energy is high if the trigger pulse is slightly delayed with respect to the pump pulses. We demonstrate that these geometry-dependent spectra and coherent-transient response can be explained by using simple models.

physics.atom-ph↗

arXiv2017

Injection seeded tunable mid-infrared pulses by difference frequency mixing

We report on the generation of nanosecond mid-infrared pulses having frequency tunability, a narrow linewidth, and a high pulse energy. These pulses are obtained by frequency mixing between injection-seeded near-infrared pulses in potassium titanyl arsenate crystals. A continuous-wave external cavity laser diode or a Ti:sapphire ring laser is used as a tunable seeding source for the near-infrared pulses. The typical energy of the generated mid-infrared pulses is in the range of 0.4-1 mJ/pulse. The tuning wavelength ranges from 3142 to 4806 nm. A narrow linewidth of 1.4 GHz and good frequency reproducibility of the mid-infrared pulses are confirmed by observing a rovibrational absorption line of gaseous carbon monoxide at 4587 nm.

physics.optics↗

arXiv2016

Vibrational two-photon emission from coherently excited solid parahydrogen

We report observation of two-photon emission from coherently excited vibrational state of solid parahydrogen, known as one of quantum solids. The coherent state between the ground and the excited states is prepared by stimulated Raman scattering using two visible laser pulses. The two-photon emission is triggered by another mid-infrared laser pulse. The observed two-photon emission persists even when the trigger pulse is injected long after the excitation. The observed phenomenon is due to a long decoherence time of the vibrational states of solid parahydrogen, which is attributed to special nature as quantum solid. Dependence of the decoherence on target temperature and residual orthohydrogen concentration are studied along with its time evolution. It is found that the emission intensity increases even after the excitation pulses pass through the target completely. The coherence development is highly suppressed at high target temperature and high residual orthohydrogen concentration. Effects of target annealing and laser-induced damage on the target are also observed.

physics.chem-ph↗

arXiv2015

Externally triggered coherent two-photon emission from hydrogen molecules

We report coherent enhancement of two-photon emission from the excited vibrational state of molecular hydrogen triggered by irradiating mid-infrared pulses externally. We previously observed the two-photon emission triggered by the internally generated fourth Stokes photons. By injecting independent mid-infrared pulses externally, it is possible to control experimental parameters and investigate the mechanism in more detail. In this article, we describe the two-photon emission using the external trigger pulses. Its spectrum and dependence on the energy and timing of the trigger pulse are presented along with numerical simulations based on the Maxwell-Bloch equations. The measured number of emitted photons is 6 10^11 photons/pulse and the resulting enhancement factor from the spontaneous emission is more than 10^18. This value is three orders of magnitude higher than that of the previous experiment. External control of emission process is expected to be essential for observation of weaker process of radiative emission of neutrino pair.

physics.atom-ph↗

arXiv2014

Observation of coherent two-photon emission from the first vibrationally-excited state of hydrogen molecules

In this paper, we describe an experiment which was conducted to explore the macro-coherent amplification mechanism using a two-photon emission process from the first vibrationally-excited state of para-hydrogen molecule. Large coherence in the initial state was prepared by the adiabatic Raman population transfer method, and the lowest Stokes sideband was used as a trigger field. We observed the coherent two-photon emission consistent with the expectation of the paired super-radiance master equation.

physics.atom-ph↗