Time-resolved Pump-probe Experiments Research Articles

Effect of photoexcitation on high-harmonic generation in semiconductors

Solid-state high-harmonic generation is intrinsically sensitive to band structure, carrier population, and carrier scattering. As such, solid-state high-harmonic generation is increasingly used as a probe for femtosecond time-resolved pump-probe experiments. So far, most experimental pump-probe studies have reported photoexcitation-induced amplitude suppression of high-harmonic generation in solid-state media, yet the origins of this phenomenon remain elusive. Through simulations based on the semiconductor Bloch equations, we identify the dephasing of the coherent carrier population as the primary mechanism driving this suppression. Furthermore, we find band gap renormalization to be a source for phase shifts of high harmonics. We introduce an analytical model, based on a semi-classical action, that supports our numerical outcomes.

Optimizing pump-probe reflectivity measurements of ultrafast photoacoustics with modulated asynchronous optical sampling.

Time-resolved optical pump-probe experiments enable the study of complex light-matter interactions on ultrafast timescales, provided that they reach sufficient sensitivity. For instance, with pump-induced ultrafast photoacoustics, probing the typically small changes in optical properties requires a high signal-to-noise ratio. Asynchronous optical sampling (ASOPS), using two separate pulsed lasers at slightly different repetition rates, can be effective at removing noise by averaging many rapidly acquired traces. However, the pump-probe delay scan with ASOPS is always as long as the pump pulse interval, which is inefficient if the delay-time range of interest is shorter. Here, we demonstrate two modified ASOPS schemes that optimize measurement efficiency by only scanning the range of interest. The modification based on frequency modulated ASOPS (MASOPS) is most efficient, especially in the presence of low-frequency flicker noise. We provide a proof-of-concept measurement of ultrafast photoacoustics in which we use MASOPS to scan a time delay of 1/20 of the pump pulse interval. The resulting noise floor is 20 times lower compared to conventional ASOPS, allowing for 20 times faster measurements. Furthermore, we show that by taking experimental noise characteristics into account, more traditional pump-probe methods can also be optimized.

Mapping extended reaction coordinates in photochemical dynamics

Laser-based experiments facilitate numerous strategies for interrogating the complex non-adiabatic dynamics operating in the excited states of molecules. Measurements may be broadly separated into frequency- and time-resolved variants, with a combination of different approaches (with different associated observables) typically being required to reveal a complete mechanistic picture. In the former category, quantum state-resolved information may often be obtained using narrow linewidth lasers. This provides detailed information relating to the starting point on the photochemical reaction coordinate (via the absorption spectrum) and the asymptotic endpoints (i.e. the photoproducts). Direct observation of the intermediate pathways connecting these two limits is often not possible, however, due to the inherently long temporal duration of the laser pulses relative to the typical timescales of non-adiabatic energy redistribution processes. It is therefore desirable to obtain complementary information that monitors real-time evolution along the reaction coordinate as excited state population traverses the potential energy landscape. This may be achieved in time-resolved pump–probe experiments conducted using ultrafast (i.e. sub-picosecond) laser pulses. The use of valence state photoionization for the probe step is a commonly employed methodology and has proved highly instructive in revealing subtle mechanistic details of key energy redistribution pathways operating in many different molecular systems. One frequent limitation here, however, is the restricted “view” along the reaction coordinate(s) connecting the initially prepared excited states to various photoproducts. Guided by examples drawn from recent work using time-resolved photoelectron imaging, this review will discuss such issues in detail and highlight some strategies that potentially help overcome them – with particular emphasis placed on the advantages of projecting as deeply as possible into the ionization continuum. The role of complementary measurements using other spectroscopic techniques and the importance of high-level supporting theory to guide data interpretation will also be reinforced.

Exciton polariton interactions in Van der Waals superlattices at room temperature

Monolayer transition-metal dichalcogenide (TMD) materials have attracted a great attention because of their unique properties and promising applications in integrated optoelectronic devices. Being layered materials, they can be stacked vertically to fabricate artificial van der Waals lattices, which offer unique opportunities to tailor the electronic and optical properties. The integration of TMD heterostructures in planar microcavities working in strong coupling regime is particularly important to control the light-matter interactions and form robust polaritons, highly sought for room temperature applications. Here, we demonstrate the systematic control of the coupling-strength by embedding multiple WS2 monolayers in a planar microcavity. The vacuum Rabi splitting is enhanced from 36 meV for one monolayer up to 72 meV for the four-monolayer microcavity. In addition, carrying out time-resolved pump-probe experiments at room temperature we demonstrate the nature of polariton interactions which are dominated by phase space filling effects. Furthermore, we also observe the presence of long-living dark excitations in the multiple monolayer superlattices. Our results pave the way for the realization of polaritonic devices based on planar microcavities embedding multiple monolayers and could potentially lead the way for future devices towards the exploitation of interaction-driven phenomena at room temperature.

Experiment and theory elucidate the pathways for H3+formation in the ultrafast double ionization in methanol

Experiment and theory elucidate the pathways for H₃⁺formation in the ultrafast double ionization in methanol

Lattice dynamics of the excitonic insulator Ta2Ni(Se1−xSx)5

Recently, we employed electronic polarization-resolved Raman spectroscopy to reveal the strongly correlated excitonic insulator (EI) nature of Ta2NiSe5, Volkov et al. [arXiv:2007.07344], and also showed that for Ta$_2$Ni(Se$_{1-x}$S$_x$)$_5$ alloys the critical excitonic fluctuations diminish with sulfur concentration x exposing a cooperating lattice instability that takes over for large x, Volkov et al. [arXiv:2104.07032]. Here we focus on the lattice dynamics of this EI family. We identify all Raman-active optical phonons of fully symmetric and ac-quadrupole-like symmetries and study their evolution with temperature and sulfur concentration. We demonstrate the change of selection rules at temperatures below the orthorhombic-to-monoclinic transition at Tc(x) that is related to the EI phase. We find that Tc(x) decrease monotonically from 328 K for Ta2NiSe5 to 120 K for Ta2NiS5 and that the magnitude of lattice distortion also decreases with the sulfur concentration x. For x < 0.7, the two lowest-frequency B2g phonon modes show strongly asymmetric lineshapes at high temperatures due to Fano interference with the broad excitonic continuum present in a semimetallic state. Within the framework of extended Fano model, we develop a quantitative description of the interacting exciton-phonon excitation lineshape, enabling us to derive the intrinsic phonon parameters and determine the exciton-phonon interaction strength, that affects the transition temperature Tc(x). We also observe signatures of the acoustic mode scattered assisted by the structural domain walls formed below Tc. Based on our results, we additionally present a consistent interpretation of the origin of oscillations observed in time-resolved pump-probe experiments.

A novel free-electron laser single-pulse Wollaston polarimeter for magneto-dynamical studies.

Here, we report on the conceptual design, the hardware realization, and the first experimental results of a novel and compact x-ray polarimeter capable of a single-pulse linear polarization angle detection in the extreme ultraviolet photon energy range. The polarimeter is tested by performing time resolved pump–probe experiments on a Ni80Fe20 Permalloy film at the M2,3 Ni edge at an externally seeded free-electron laser source. Comparison with similar experiments reported in the literature shows the advantages of our approach also in view of future experiments.

Real-time observation of ultrafast molecular rotation in weakly bound dimers

The fragmentation dynamics of dicationic dimers of acetylene molecules initiated upon strong-field laser ionization is studied. Time-resolved pump-probe experiments with femtosecond laser pulses, accompanied by ab initio dynamical calculations, allow us to evaluate the detailed behavior of molecular ions during the dissociation process. The dynamical properties of the intermediate C2H2+⋯C2H2+ state created by the pump pulse are probed by a second pulse which causes further ionization. The time-dependent yield of a coincident C2H2+ + C2H22+ ion pair exhibits an oscillation feature with a periodicity of 240 ± 30 fs. Our studies demonstrate that this is caused by an ultrafast rotation of C2H2+ cations driven by intermolecular Coulomb force together with the orientation-dependent ionization rate. We suggest that the present observation of ultrafast molecular rotation can be a general phenomenon occurring in a wide variety of systems.Received 14 September 2020Accepted 31 March 2021DOI:https://doi.org/10.1103/PhysRevResearch.3.023050Published by the American Physical Society under the terms of the Creative Commons Attribution 4.0 International license. Further distribution of this work must maintain attribution to the author(s) and the published article's title, journal citation, and DOI. Open access publication funded by the Max Planck Society.Published by the American Physical SocietyPhysics Subject Headings (PhySH)Research AreasLaser-cluster interactionUltrafast phenomenaVan der Waals interactionAtomic, Molecular & Optical

Generation of ultrashort keV Ar+ ion pulses via femtosecond laser photoionization

Ion beams with energies in the keV regime are widely utilized in solid-state physics, but the ultrafast dynamics triggered by an ion impact onto a solid surface is to date exclusively accessible via simulations based on many untested assumptions and model parameters. A possible experimental access rests on the availability of a laser-synchronized ion source delivering sufficiently short ion pulses for time resolved pump–probe experiments. Here, we demonstrate a new miniaturized ion optical bunching setup for the creation of rare gas ion pulses using strong-field femtosecond laser photoionization. Neutral Ar gas atoms at room temperature are intercepted by a 50 fs, 800 nm laser pulse focused to ∼10 μm spot size. We demonstrate the generation of monoenergetic 2 keV Ar+ ion pulses with 180 ps duration (FWHM) at laser peak intensities around 1014 W cm−2 and of multiply charged Ar q+ ions (q = 1–5) at higher laser intensities. The results are in good agreement with detailed ion trajectory simulations, which show that the temporal resolution is essentially limited by the initial (thermal) velocity spread of the generated photo-ions, indicating the possibility to achieve even better time resolution by cooling the gas prior to ionization.

Nanoparticle-Fluid Interactions at Ultrahigh Acoustic Vibration Frequencies Studied by Femtosecond Time-Resolved Microscopy.

Liquid viscous and viscoelastic properties are very important parameters in determining rheological phenomena. Mechanical resonators with extremely high vibrational frequencies interacting with simple liquids present a wide range of applications from mass sensing to biomechanics. However, a lack of understanding of fluid viscoelasticity greatly hinders the utilization of mechanical resonators. In this paper, the high frequency acoustic vibrations of Au nanoplates with large quality factors were used to probe fluid properties (water, glycerol, and their mixtures) through time-resolved pump-probe microscopy experiments. For water, viscous damping was clearly observed, where an inviscid effect was only detected previously. Adding glycerol to the water increases the fluid viscosity and leads to a bulk viscoelastic response in the system. The experimental results are in excellent agreement with a continuum mechanics model for the damping of nanoplate breathing modes in liquids, confirming the experimental observation of viscoelastic effects. In addition to the breathing modes of the nanoplates, Brillouin oscillations are observed in the experiments. Analysis of the frequency of the Brillouin oscillations also shows the presence of viscoelastic effects in the high-viscosity solvents. The detection and analysis of viscous damping in liquids is important not only for understanding the energy dissipation mechanisms and providing the mechanical relaxation times of the liquids but also for developing applications of nanomechanical resonators for fluid environments.

Ultrafast strain engineering and coherent structural dynamics from resonantly driven optical phonons in LaAlO3

Strain engineering has been extended recently to the picosecond timescales, driving ultrafast metal–insulator phase transitions and the propagation of ultrasonic demagnetization fronts. However, the nonlinear lattice dynamics underpinning interfacial optoelectronic phase switching have not yet been addressed. Here we perform time-resolved all-optical pump-probe experiments to study ultrafast lattice dynamics initiated by impulsive light excitation tuned in resonance with a polar lattice vibration in LaAlO3 single crystals, one of the most widely utilized substrates for oxide electronics. We show that ionic Raman scattering drives coherent rotations of the oxygen octahedra around a high-symmetry crystal axis. By means of DFT calculations we identify the underlying nonlinear phonon–phonon coupling channel. Resonant lattice excitation is also shown to generate longitudinal and transverse acoustic wave packets, enabled by anisotropic optically induced strain. Importantly, shear strain wave packets are found to be generated with high efficiency at the phonon resonance, opening exciting perspectives for ultrafast material control.

Time-resolved ultrafast dynamics in triple degenerate topological semimetal molybdenum phosphide

We employ the time resolved pump probe experiment to investigate the ultrafast dynamics in a topological semimetal molybdenum phosphide (MoP), which exhibits triple degenerate points in the momentum space. Two relaxation processes with the lifetime of 0.3 and 150 ps have been observed. We attribute the fast component to the electron-phonon scattering and the slow component to the phonon-phonon scattering, respectively. Temperature dependence investigation shows that both the lifetimes of the fast and slow components enhance slightly with increasing temperature. We also successfully generate and detect a thermal-stress-induced coherent acoustic phonon mode with a frequency of 0.033 THz, which does not vary with temperature. Our ultrafast spectroscopy investigation of the quasiparticle dynamics and the coherent phonon in MoP provides useful experimental facts and information about the overall excited state dynamics and the temperature dependence of electron-phonon coupling.

Origin of Broad Emission Spectra in InP Quantum Dots: Contributions from Structural and Electronic Disorder.

The ensemble emission spectra of colloidal InP quantum dots are broader than achievable spectra of cadmium- and lead-based quantum dots, despite similar single-particle line widths and significant efforts invested in the improvement of synthetic protocols. We seek to explain the origin of persistently broad ensemble emission spectra of colloidal InP quantum dots by investigating the nature of the electronic states responsible for luminescence. We identify a correlation between red-shifted emission spectra and anomalous broadening of the excitation spectra of luminescent InP colloids, suggesting a trap-associated emission pathway in highly emissive core-shell quantum dots. Time-resolved pump-probe experiments find that electrons are largely untrapped on photoluminescence relevant time scales pointing to emission from recombination of localized holes with free electrons. Two-dimensional electronic spectroscopy on InP quantum dots reveals multiple emissive states and increased electron-phonon coupling associated with hole localization. These localized hole states near the valence band edge are hypothesized to arise from incomplete surface passivation and structural disorder associated with lattice defects. We confirm the presence and effect of lattice disorder by X-ray absorption spectroscopy and Raman scattering measurements. Participation of localized electronic states that are associated with various classes of lattice defects gives rise to phonon-coupled defect related emission. These findings explain the origins of the persistently broad emission spectra of colloidal InP quantum dots and suggest future strategies to narrow ensemble emission lines comparable to what is observed for cadmium-based materials.

Crystallography on a chip - without the chip: sheet-on-sheet sandwich.

Crystallography chips are fixed-target supports consisting of a film (for example Kapton) or wafer (for example silicon) that is processed using semiconductor-microfabrication techniques to yield an array of wells or through-holes in which single microcrystals can be lodged for raster-scan probing. Although relatively expensive to fabricate, chips offer an efficient means of high-throughput sample presentation for serial diffraction data collection at synchrotron or X-ray free-electron laser (XFEL) sources. Truly efficient loading of a chip (one microcrystal per well and no wastage during loading) is nonetheless challenging. The wells or holes must match the microcrystal size of interest, requiring that a large stock of chips be maintained. Raster scanning requires special mechanical drives to step the chip rapidly and with micrometre precision from well to well. Here, a `chip-less' adaptation is described that essentially eliminates the challenges of loading and precision scanning, albeit with increased, yet still relatively frugal, sample usage. The device consists simply of two sheets of Mylar with the crystal solution sandwiched between them. This sheet-on-sheet (SOS) sandwich structure has been employed for serial femtosecond crystallography data collection with micrometre-sized crystals at an XFEL. The approach is also well suited to time-resolved pump-probe experiments, in particular for long time delays. The SOS sandwich enables measurements under XFEL beam conditions that would damage conventional chips, as documented here. The SOS sheets hermetically seal the sample, avoiding desiccation of the sample provided that the X-ray beam does not puncture the sheets. This is the case with a synchrotron beam but not with an XFEL beam. In the latter case, desiccation, setting radially outwards from each punched hole, sets lower limits on the speed and line spacing of the raster scan. It is shown that these constraints are easily accommodated.

Carrier-Induced Coherent Phonon Softening in Bismuth

With performing time-resolved pump-probe experiments with ultrashort pulses from a mode-locked Ti:sapphire laser, we report on the carrier-induced softening and dephasing of coherent phonon oscillations in the bismuth crystal. As the lattice displacement becomes severe at high pump power, a frequency shift can occur due to the lattice anharmonicity term. We clarified from the measurements done by varying the pulse duration that the phonon softening at high pump intensity in bismuth originates from the electron-interaction of photoexcited carriers not from the phonon anharmonicity. We also find that the coherent phonon dephasing is accelerated at high carrier densities.

Role of geminate electron-hole pairs in the time-resolved terahertz spectroscopy of organic semiconductors

Losses of the terahertz (THz) radiation energy transmitted through an organic semiconductor are examined for the time-resolved pump-probe experiments, in which electrons and holes are produced by the pump femtosecond laser pulse followed by the action of the THz probe pulse with duration of the order of 1 ps. Non-stationary electric polarization of electron-hole pairs by the electric field of THz probe pulse is considered to be responsible for the THz energy losses. The relative decrease of the THz energy density is found as a function of the sum of the electron – hole mobilities and delay time of the probe pulse with respect to the pump one.

Photo-excited dynamics in the excitonic insulator Ta2NiSe5

The excitonic insulator is an intriguing correlated electron phase formed of condensed excitons. A promising candidate is the small band gap semiconductor Ta2NiSe5. Here we investigate the quasiparticle and coherent phonon dynamics in Ta2NiSe5 in a time resolved pump probe experiment. Using the models originally developed by Kabanov et al for superconductors (Kabanov et al 1999 Phys. Rev. B 59 1497), we show that the material’s intrinsic gap can be described as almost temperature independent for temperatures up to about 250 K to 275 K. This behavior supports the existence of the excitonic insulator state in Ta2NiSe5. The onset of an additional temperature dependent component to the gap above these temperatures suggests that the material is located in the BEC-BCS crossover regime. Furthermore, we show that this state is very stable against strong photoexcitation, which reveals that the free charge carriers are unable to effectively screen the attractive Coulomb interaction between electrons and holes, likely due to the quasi 1D structure of Ta2NiSe5.

All-optical in-depth detection of the acoustic wave emitted by a single gold nanorod

Asingle gold nanorod dropped on the surface of a silica substrate is used as a transient optoacoustic source of gigahertz hypersounds.We demonstrate the all-optical detection of the as-generated acousticwave front propagating in the silica substrate. For this purpose, time-resolved femtosecond pump-probe experiments are performed in a reflection configuration. The fundamental breathing mode of the nanorod is detected at 23 GHz by interferometry, and the longitudinal acousticwave radiated in the silica substrate is detected by time-resolved Brillouin scattering. By tuning the optical probe wavelength from 750 to 900 nm, hypersounds with wavelengths of 260–315 nm are detected in the silica substrate, with corresponding acoustic frequencies in the range of 19–23 GHz. To confirm the origin of these hypersounds, we theoretically analyze the influence of the acoustic excitation spectrum on the temporal envelope of the transient reflectivity. This analysis proves that the acoustic wave detected in the silica substrate results from the excitation of the breathing mode of the nanorod. These results pave the way for performing local in-depth elastic nanoscopy.

Excited-state dissociation dynamics of phenol studied by a new time-resolved technique

Phenol is an important model molecule for the theoretical and experimental investigation of dissociation in the multistate potential energy surfaces. Recent theoretical calculations [X. Xu et al., J. Am. Chem. Soc. 136, 16378 (2014)] suggest that the phenoxyl radical produced in both the X and A states from the O-H bond fission in phenol can contribute substantially to the slow component of photofragment translational energy distribution. However, current experimental techniques struggle to separate the contributions from different dissociation pathways. A new type of time-resolved pump-probe experiment is described that enables the selection of the products generated from a specific time window after molecules are excited by a pump laser pulse and can quantitatively characterize the translational energy distribution and branching ratio of each dissociation pathway. This method modifies conventional photofragment translational spectroscopy by reducing the acceptance angles of the detection region and changing the interaction region of the pump laser beam and the molecular beam along the molecular beam axis. The translational energy distributions and branching ratios of the phenoxyl radicals produced in the X, A, and B states from the photodissociation of phenol at 213 and 193 nm are reported. Unlike other techniques, this method has no interference from the undissociated hot molecules. It can ultimately become a standard pump-probe technique for the study of large molecule photodissociation in multistates.

Instrumental development of a quasi-relativistic ultrashort electron beam source for electron diffractions and spectroscopies.

A stable femtosecond electron beam system has been configured for time-resolved pump-probe experiments. The ultrafast electron diffraction (UED) system is designed with a sub-MeV photoelectron beam source pulsed by a femtosecond UV laser and nondispersive beamline components, including a bunch compressor-a pulsed S-band klystron is installed and fully commissioned with 5.5 MW peak power in a 2.5 μs pulse length. A single-cell RF photo-gun is designed to produce 1.6-16 pC electron bunches in a photoemission mode with 150 fs pulse duration at 0.5-1 MeV. The measured RF system jitters are within 1% in magnitude and 0.2° in phase, which would induce 3.4 keV and 0.25 keV of ΔE, corresponding to 80 fs and 5 fs of Δt, respectively. Our particle-in-cell simulations indicate that the designed bunch compressor reduces the time-of-arrival jitter by about an order of magnitude. The transport and focusing optics of the designed beamline with the bunch compressor enables an energy spread within 10-4 and a bunch length (electron probe) within <500 fs. In this paper, the design analysis and instrumental test results are presented along with the development of the quasi-relativistic UED system.