arXiv subjects

Teruto Kanai

Publications and source records attributed to Teruto Kanai.

12 recordsLinked to original sources

arXiv2025

Distinct amplitude mode dynamics upon resonant and off-resonant excitation across the charge density wave energy gap in LaTe3 investigated by time- and angle-resolved photoemission spectroscopy

Non-equilibrium states generated by ultrafast laser pulses are characterized by specific phenomena that are not accessible in static measurements. Previous time- and angle-resolved photoemission spectroscopy (TARPES) studies on rare-earth tritelluride materials have revealed the laser-driven melting of the charge density wave order as well as its collective amplitude mode excitation. Variation of the excess energy deposited by optical pumping in the material promises pathways to control the dynamic material response. To this end, we use an optical parametric amplifier to generate a tunable pump photon energy. Studying LaTe3 we compare the dynamics driven by pumping resonantly across the charge density wave energy gap with the effect of pumping at a twice higher photon energy in a TARPES pump-probe experiment. We clearly identify a pump photon energy dependent behavior. At the larger pump photon energy, the excess electronic energy generates lattice heating mediated by e-ph coupling and softening of the amplitude mode frequency from 3 to 2 THz. Remarkably, the resonant pumping across the CDW gap results in a time-independent amplitude mode frequency. We conclude that the resonant excitation across the energy gap excites the amplitude mode selectively while additional electronic excess energy deposited at higher pump photon energy modifies the crystal properties transiently by incoherent dissipative processes.

cond-mat.str-el↗

arXiv2024

Unveiling van Hove singularity modulation and fluctuated charge order in kagome superconductor $\rm{CsV_3Sb_5}$ via time-resolved ARPES

Kagome superconductor CsV3Sb5, which exhibits intertwined unconventional charge density wave (CDW) and superconductivity, has garnered significant attention recently. Despite extensive static studies, the nature of these exotic electronic orders remains elusive. In this study, we investigate the non-equilibrium electronic structure of CsV3Sb5 via time- and angle-resolved photoemission spectroscopy. Our results reveal that upon laser excitation, the van Hove singularities immediately shift towards the Fermi level and subsequently oscillate in sync with a 1.3 THz coherent phonon mode. By analyzing the coherent intensity oscillations in the energy-momentum (E-k) map, we find that this coherent phonon is strongly coupled with electronic bands from both Sb and V orbitals. While typically observable only in the CDW state, remarkably, we find that the 1.3-THz coherent phonon mode can be persistently excited at temperatures above T_CDW, suggesting the potential existence of fluctuated CDW in CsV3Sb5. These findings enhance our understanding of the unconventional CDW control of kagome superconductivity.

cond-mat.mtrl-sci↗

arXiv2024

Time- and angle-resolved photoemission spectroscopy with wavelength-tunable pump and extreme ultraviolet probe enabled by twin synchronized amplifiers

We describe a setup for time- and angle-resolved photoemission spectroscopy with wavelength-tunable excitation and extreme ultraviolet probe. It is enabled by using the 10 kHz twin Ti:sapphire amplifiers seeded by the common Ti:sapphire oscillator. The typical probe energy is 21.7 eV, and the wavelength of the pump excitation is tuned between 2400 and 1200 nm by using the optical parametric amplifier. The total energy resolution of 133 meV is achieved, and the time resolution is dependent on the wavelength for the pump, typically better than 100 fs. This system enables the pump energy to be matched with a specific interband transition and to probe a wider energy-momentum space. We present the results for the prototypical materials of highly oriented pyrolytic graphite and Bi2Se3 to show the performance of our system.

cond-mat.mtrl-sci↗

arXiv2022

Photo-induced nonlinear band shift and valence transition in SmS

The photo-induced band structure variation of a rare-earth-based semiconductor, samarium monosulfide (SmS), was investigated using high-harmonic-generation laser-based time-resolved photoelectron spectroscopy. A nonlinear photo-induced band shift of the Sm 4f multiplets was observed. The first one is a shift to the high-binding-energy side due to a large surface photovoltage (SPV) effect of approximately 93 meV, comparable to the size of the bulk band gap, with a much longer relaxation time than 0.1 ms. The second one is an ultrafast band shift to the low binding energy side, which is in the opposite direction to the SPV shift, suggesting an ultrafast valence transition from divalent to trivalent Sm ions due to photo-excitation. The latter energy shift was approximately 58 meV, which is consistent with the energy gap shift from ambient pressure to the boundary between the black insulator and golden metallic phase with the application of pressure. This suggests that the photo-induced valence transition can reach the phase boundary, but other effects are necessary to realize the golden metallic phase.

cond-mat.mtrl-sci↗

arXiv2022

Direct observation of multiple conduction-band minima in high-performance thermoelectric SnSe

We report time- and angle-resolved photoemission spectroscopy on SnSe which currently attracts great interest due to its extremely high thermoelectric performance. Laser-assisted photoemission signals are observed within $\pm$20 fs of the pump pulse arrival. Around 30-50 fs after the photoexcitation, the conduction band minima are not populated by the photoexcited electrons while the valence bands are considerably broadened. In going from 90 fs to 550 fs after the photoexcitation, the photoexcited carriers are decayed into the multiple conduction band minima. The observed conduction bands are consistent with the band structure calculations. The multiple conduction minima suggest possibility of high and anisotropic thermoelectric performance of n-type SnSe single crystal if it is realized.

cond-mat.mtrl-sci↗

arXiv2020

Photo-excitation band-structure engineering of 2H-NbSe$_2$ probed by time- and angle-resolved photoemission spectroscopy

We investigated the nonequilibrium electronic structure of 2H-NbSe$_2$ by time- and angle-resolved photoemission spectroscopy. We find that the band structure is distinctively modulated by strong photo-excitation, as indicated by the unusual increase in the photoelectron intensities around E$_F$. In order to gain insight into the observed photo-induced electronic state, we performed DFT calculations with modulated lattice structures, and found that the variation of the Se height from the Nb layer results in a significant change in the effective mass and band gap energy. We further study the momentum-dependent carrier dynamics. The results suggest that the relaxation is faster at the K-centered Fermi surface than at the $Γ$-centered Fermi surface, which can be attributed to the stronger electron-lattice coupling at the K-centered Fermi surface. Our demonstration of band structure engineering suggests a new role for light as a tool for controlling the functionalities of solid-state materials.

cond-mat.str-el↗

arXiv2020

Detecting electron-phonon couplings during photo-induced phase transition

Photo-induced phase transitions have been intensively studied owing to the ability to control a material of interest in the ultrafast manner, which can induce exotic phases unable to be attained at equilibrium. However, the key mechanisms are still under debate, and it has currently been a central issue how the couplings between the electron, lattice, and spin degrees of freedom are evolving during photo-induced phase transitions. Here, we develop a new analysis method, frequency-domain angle-resolved photoemission spectroscopy, to gain precise insight into electron-phonon couplings during photo-induced insulator-to-metal transitions for Ta$_2$NiSe$_5$. We demonstrate that multiple coherent phonons generated by displacive excitations show band-selective coupling to the electrons. Furthermore, we find that the lattice modulation corresponding to the 2 THz phonon mode, where Ta lattice is sheared along the a-axis, is the most relevant for the photo-induced semimetallic state.

cond-mat.str-el↗

arXiv2020

High-harmonic generation in GaAs beyond the perturbative regime

We experimentally study the field-intensity dependence of high-harmonic generation in bulk gallium arsenide in reflection geometry. We find the oscillatory behavior at high fields where a perturbative scaling law no longer holds. By constructing a theoretical framework based on the Luttinger-Kohn model, we succeed in reproducing the observed oscillatory behavior. The qualitative agreement between the experiment and theory indicates that field-induced dynamic band modification is crucial in the nonperturbative regime. We consider the origin of the oscillatory behavior in terms of dynamical localization based on the Floquet subband picture.

cond-mat.mes-hall↗

arXiv2019

Real-time observation of electronic, vibrational, and rotational dynamics in nitric oxide with attosecond soft X-ray pulses at 400 eV

Photoinduced quantum dynamics in molecules have hierarchical temporal structures with different energy scales that are associated with electron and nuclear motions. Femtosecond-to-attosecond transient absorption spectroscopy (TAS) using high-harmonic generation (HHG) with a photon energy below 300 eV has been a powerful tool to observe such electron and nuclear dynamics in a table-top manner. However, comprehensive measurements of the electronic, vibrational, and rotational molecular dynamics have not yet been achieved. Here, we demonstrate HHG-based TAS at the nitrogen K-edge (400 eV) for the first time, and observe all the electronic, vibrational, and rotational degrees of freedom in a nitric oxide molecule at attosecond to sub-picosecond time scales. This method of employing core-to-valence transitions offers an all-optical approach to reveal complete molecular dynamics in photochemical reactions with element and electronic state specificity.

physics.atom-ph↗

arXiv2019

Photo-induced Superconducting State with Long-lived Disproportionate Band Filling in FeSe

Photo-excitation is a very powerful way to instantaneously drive a material into a novel quantum state without any fabrication, and variable ultrafast techniques have been developed to observe how electron-, lattice-, and spin-degrees of freedom change. One of the most spectacular phenomena is photo-induced superconductivity, and it has been suggested in cuprates that the transition temperature Tc can be enhanced from original Tc with significant lattice modulations. Here we show another photo-induced high-Tc superconducting state in the iron-based superconductor FeSe with semi-metallic hole and electron bands. The transient electronic state in the entire Brillouin zone is directly observed by the time- and angle-resolved photoemission spectroscopy using extreme ultraviolet pulses obtained from high harmonic generation. Our results of dynamical behaviors on timescales from 50 fs to 800 ps consistently support the favorable superconducting state after photo-excitation well above Tc. This finding demonstrates that multiband iron-based superconductors emerge as an alternative candidate for photo-induced superconductors.

cond-mat.supr-con↗

arXiv2018

Photo-induced semimetallic states realised in electron-hole coupled insulators

Using light to manipulate materials into desired states is one of the goals in condensed matter physics, since light control can provide ultrafast and environmentally-friendly photonics devices. However, it is generally difficult to realise a photo-induced phase which is not merely a higher entropy phase corresponding to a high-temperature phase at equilibrium. Here, we report realization of photo-induced insulator-to-metal transitions in Ta2Ni(Se1-xSx)5 including the excitonic insulator phase using time- and angle-resolved photoemission spectroscopy. From the dynamic properties of the system, we determine that screening of excitonic correlations plays a key role in the timescale of the transition to the metallic phase, which supports the existence of an excitonic-insulator phase at equilibrium. The non-equilibrium metallic state observed unexpectedly in the direct-gap excitonic insulator opens up a new avenue to optical band engineering in electron-hole coupled systems.

cond-mat.mtrl-sci↗

arXiv2018

Antiphase Fermi-surface modulations accompanying displacement excitation in a parent compound of iron-based superconductors

We investigate the transient electronic structure of BaFe2As2, a parent compound of iron-based superconductors, by time- and angle-resolved photoemission spectroscopy. In order to probe the entire Brillouin zone, we utilize extreme ultraviolet photons and observe photoemission intensity oscillation with the frequency of the A1g phonon which is antiphase between the zone-centered hole Fermi surfaces (FSs) and zone-cornered electron FSs. We attribute the antiphase behavior to the warping in one of the zone-centered hole FSs accompanying the displacement of the pnictogen height, and find that this displacement is the same direction as that induced by substitution of P for As, where superconductivity is induced by a structural modification without carrier doping in this system.

cond-mat.supr-con↗