arXiv subjects

Keith A. Nelson

Publications and source records attributed to Keith A. Nelson.

At least 37 records · Page 2Linked to original sources

arXiv2024

Hard X-ray Generation and Detection of Nanometer-Scale Localized Coherent Acoustic Wave Packets in SrTiO$_3$ and KTaO$_3$

We demonstrate that the absorption of femtosecond x-ray pulses can excite quasi-spherical high-wavevector coherent acoustic phonon wavepackets using an all x-ray pump and probe scattering experiment. The time- and momentum-resolved diffuse scattering signal is consistent with strain pulses induced by the rapid electron cascade dynamics following photoionization at uncorrelated excitation centers. We quantify key parameters of this process, including the localization size of the strain wavepacket and the energy absorption efficiency, which are determined by the photoelectron and Auger electron cascade dynamics, as well as the electron-phonon interaction. In particular, we obtain the localization size of the observed strain wave packet to be 1.5 and 2.5 nm for bulk SrTiO$_3$ and KTaO$_3$ single crystals, even though there are no nanoscale structures or light-intensity patterns that would ordinarily be required to generate acoustic waves of wavelengths much shorter than the penetration depth. Whereas in GaAs and GaP we do not observe a signal above background. The results provide crucial information on x-ray matter interactions, which sheds light on the mechanism of x-ray energy deposition, and the study of high wavevector acoustic phonons and thermal transport at the nanoscale.

cond-mat.mtrl-sci↗

arXiv2023

Optical-pump terahertz-probe spectroscopy in high magnetic fields with kHz single-shot detection

We demonstrate optical pump/THz probe (OPTP) spectroscopy with a variable external magnetic field (0-9 T) in which the time-dependent THz signal is measured by echelon-based single-shot detection at a 1 kHz repetition rate. The method reduces data acquisition times by more than an order of magnitude compared to conventional electro-optic sampling using a scanning delay stage. The approach illustrates the wide applicability of the single-shot measurement approach to nonequilibrium systems that are studied through OPTP spectroscopy, especially in cases where parameters such as magnetic field strength (B) or other experimental parameters are varied. We demonstrate the capabilities of our measurement by performing cyclotron resonance experiments in bulk silicon, where we observe B-field dependent carrier relaxation and distinct relaxation rates for different carrier types. We use a pair of economical linear array detectors to measure 500 time points on each shot, offering equivalent performance to camera-based detection with possibilities for higher repetition rates.

physics.optics↗

arXiv2023

High-power laser beam shaping using a metasurface for shock excitation and focusing at the microscale

Achieving high repeatability and efficiency in laser-induced strong shock wave excitation remains a significant technical challenge, as evidenced by the extensive efforts undertaken at large-scale national laboratories to optimize the compression of light element pellets. In this study, we propose and model a novel optical design for generating strong shocks at a tabletop scale. Our approach leverages the spatial and temporal shaping of multiple laser pulses to form concentric laser rings on condensed matter samples. Each laser ring initiates a two-dimensional focusing shock wave that overlaps and converges with preceding shock waves at a central point within the ring. We present preliminary experimental results for a single ring configuration. To enable high-power laser focusing at the micron scale, we demonstrate experimentally the feasibility of employing dielectric metasurfaces with exceptional damage threshold, experimentally determined to be 1.1 J/cm2, as replacements for conventional optics. These metasurfaces enable the creation of pristine, high-fluence laser rings essential for launching stable shock waves in materials. Herein, we showcase results obtained using a water sample, achieving shock pressures in the gigapascal (GPa) range. Our findings provide a promising pathway towards the application of laser-induced strong shock compression in condensed matter at the microscale.

physics.optics↗

arXiv2023

Additive Laser Excitation of Giant Nonlinear Surface Acoustic Wave Pulses

The laser ultrasonics technique perfectly fits the needs for non-contact, non-invasive, non-destructive mechanical probing of samples of mm to nm sizes. This technique is however limited to the excitation of low-amplitude strains, below the threshold for optical damage of the sample. In the context of strain engineering of materials, alternative optical techniques enabling the excitation of high amplitude strains in a non-destructive optical regime are seeking. We introduce here a non-destructive method for laser-shock wave generation based on additive superposition of multiple laser-excited strain waves. This technique enables strain generation up to mechanical failure of a sample at pump laser fluences below optical ablation or melting thresholds. We demonstrate the ability to generate nonlinear surface acoustic waves (SAWs) in Nb:SrTiO$_3$ substrates, at typically 1 kHz repetition rate, with associated strains in the percent range and pressures close to 100 kbars. This study paves the way for the investigation of a host of high-strength SAW-induced phenomena, including phase transitions in conventional and quantum materials, plasticity and a myriad of material failure modes, chemistry and other effects in bulk samples, thin layers, or two-dimensional materials.

cond-mat.mtrl-sci↗

arXiv2023

Terahertz field-driven magnon upconversion in an antiferromagnet

Tailored light excitation and nonlinear control of lattice vibrations have emerged as powerful strategies to manipulate the properties of quantum materials out of equilibrium. Generalizing the use of coherent phonon-phonon interactions to nonlinear couplings among other types of collective modes would open unprecedented opportunities in the design of novel dynamic functionalities in solids. For example, the collective excitations of magnetic order -- magnons -- can carry information with little energy dissipation, and their coherent and nonlinear control would provide an attractive route to achieve collective-mode-based information processing and storage in forthcoming spintronics and magnonics. Here, we discover that intense terahertz (THz) fields can initiate processes of magnon upconversion mediated by an intermediate magnetic resonance. By using a suite of advanced spectroscopic tools, including a newly demonstrated two-dimensional (2D) THz polarimetry technique enabled by single-shot detection, we unveil the unidirectional nature of coupling between distinct magnon modes of a canted antiferromagnet. Calculations of spin dynamics further suggest that this coupling is a universal feature of antiferromagnets with canted magnetic moments. These results demonstrate a route to inducing desirable energy transfer pathways and THz-induced coupling between coherent magnons in solids and pave the way for a new era in the development of ultrafast control of magnetism.

cond-mat.mtrl-sci↗

arXiv2023

Discovery of enhanced lattice dynamics in a single-layered hybrid perovskite

Layered hybrid perovskites have attracted much attention in recent years due to their emergent physical properties and exceptional functional performances, but the coexistence of lattice order and structural disorder severely hinders our understanding of these materials. One unsolved problem regards how the lattice dynamics are affected by the dimensional engineering of the inorganic frameworks and the interaction with the molecular moieties. Here, we address this question by using a combination of high-resolution spontaneous Raman scattering, high-field terahertz spectroscopy, and molecular dynamics simulations. This approach enables us to reveal the structural vibrations and disorder in and out of equilibrium and provides surprising observables that differentiate single- and double-layered perovskites. While no distinct vibrational coherence is observed in double-layer perovskites, we discover that an off-resonant terahertz pulse can selectively drive a long-lived coherent phonon mode through a two-photon process in the single-layered system. This difference highlights the dramatic change in the lattice environment as the dimension is reduced. The present findings pave the way for the ultrafast structural engineering of hybrid lattices as well as for developing high-speed optical modulators based on layered perovskites.

cond-mat.mtrl-sci↗

arXiv2022

Intrinsic 1T' phase induced in atomically thin 2H-MoTe$_2$ by a single terahertz pulse

Polymorphic transitions in layered transition metal dichalcogenides provide an excellent platform for discovering exotic phenomena associated with metastable states, ranging from topological phase transitions to enhanced superconductivity. In particular, the transition from 2H to 1T'-MoTe$_2$, which was thought to be induced by high-energy photon irradiation among many other means, has been intensely studied for its technological relevance in nanoscale transistors. Despite the remarkable electrical performance arising from this 2H-to-1T' transition, it remains controversial whether a crystalline 1T' phase is produced because optical signatures of this putative transition are found to be associated with the formation of elemental Te clusters instead. Here, we demonstrate the creation of an intrinsic 1T' lattice after irradiating a mono- or few-layer 2H-MoTe$_2$ with a single field-enhanced terahertz pulse, whose low photon energy limits possible structural damage by optical pulses. To visualize the temporal evolution of this irreversible transition, we further develop a single-shot terahertz pump-second harmonic probe technique, and we find that the transition out of the 2H phase occurs within 10 ns after photoexcitation. Our results not only resolve the long-standing debate over the light-induced polymorphic transition in MoTe$_2$, they also highlight the unique capability of strong-field terahertz pulses in manipulating the structure of quantum materials.

cond-mat.mes-hall↗

arXiv2022

Enhanced thermalization of exciton-polaritons in optically generated potentials

Equilibrium Bose-Einstein condensation of exciton-polaritons, demonstrated with a long-lifetime microcavity [Phys. Rev. Lett. 118, 016602 (2017)], has proven that driven-dissipative systems can undergo thermodynamic phase transitions in the limit where the quasiparticle lifetime exceeds the thermalization time. Here, we identify the role of dimensionality and polariton interactions in determining the degree of thermalization in optically generated traps. To distinguish the effect of trapping from interactions and lifetimes, we measured the polariton distribution under four nonresonant Gaussian pumps in a square geometry and compared it with polariton distributions measured with each pump individually. We found that significant redistribution of polaritons arises by trapping and modification of the density of states. Surprisingly efficient polariton-polariton scattering below the condensation threshold is evidenced by the depletion of the inflection-point polaritons. Our work provides a deeper understanding of polariton distributions and their interactions under various geometries of optically generated potentials.

cond-mat.quant-gas↗

arXiv2022

Nonlinear optical absorption in nanoscale films revealed through ultrafast acoustics

Herein we describe a novel spinning pump-probe photoacoustic technique developed to study nonlinear absorption in thin films. As a test case, an organic polycrystalline thin film of quinacridone, a well-known pigment, with a thickness in the tens of nanometers range, is excited by a femtosecond laser pulse which generates a time-domain Brillouin scattering signal. This signal is directly related to the strain wave launched from the film into the substrate and can be used to quantitatively extract the nonlinear optical absorption properties of the film itself. Quinacridone exhibits both quadratic and cubic laser fluence dependence regimes which we show to correspond to two- and three-photon absorption processes. This technique can be broadly applied to materials that are difficult or impossible to characterize with conventional transmittance-based measurements including materials at the nanoscale, prone to laser damage, with very weak nonlinear properties, opaque or highly scattering.

physics.optics↗

arXiv2022

Snapshots of a light-induced metastable hidden phase driven by the collapse of charge order

Nonequilibrium hidden states, both transient and long-lived, provide a unique window into thermally inaccessible regimes of strong coupling between microscopic degrees of freedom in quantum materials. Understanding the physical origin of these states is of both fundamental and practical significance, allowing the exploration of far-from-equilibrium thermodynamics and the development of optoelectronic devices with on-demand photoresponses. However, mapping the ultrafast formation of a long-lived hidden phase remains a long-standing challenge in physics since the initial state of the system is not recovered rapidly and conventional pump-probe methods are thus not applicable. Here, using a suite of state-of-the-art single-shot spectroscopy techniques, we present a direct ultrafast visualization of the photoinduced phase transition to both transient and long-lived hidden states in an electronic crystal, 1T-TaS2. Capturing the dynamics of this complex phase transformation in a single-shot fashion demonstrates a commonality in microscopic pathways, driven by the collapse of charge order, that the system undergoes to enter the hidden state and provides unambiguous spectral fingerprints that distinguish such state from thermally accessible phases. We present a theory of fluctuation-dominated process that explains both the dynamics and the nature of the metastable state. Our results settle the debate around the origin of this elusive metastable state and pave the way for the discovery of new quantum phases of matter.

cond-mat.str-el↗

arXiv2021

Terahertz Field-Induced Reemergence of Quenched Photoluminescence in Quantum Dots

Continuous and concerted development of colloidal quantum-dot light-emitting diodes over the past two decades has established them as a bedrock technology for the next generation of displays. However, a fundamental issue that limits the performance of these devices is the quenching of photoluminescence due to excess charges from conductive charge transport layers. Although device designs have leveraged various workarounds, doing so often comes at the cost of limiting efficient charge injection. Here we demonstrate that high-field terahertz (THz) pulses can dramatically brighten quenched QDs on metallic surfaces, an effect which persists for minutes after THz irradiation. This phenomenon is attributed to the ability of the THz field to remove excess charges, thereby reducing trion and non-radiative Auger recombination. Our findings show that THz technologies can be used to suppress and control such undesired non-radiative decay, potentially in a variety of luminescent materials for future device applications.

cond-mat.mes-hall↗

arXiv2021

Green's Functions of the Boltzmann Transport Equation with the Full Scattering Matrix for Phonon Nanoscale Transport beyond the Relaxation Time Approximation

The phonon Boltzmann transport equation (BTE) has been widely utilized to study thermal transport in solids. While for a number of materials the exact solution to the BTE has been obtained for a uniform heat flow, problems arising in micro/nanoscale heat transport have been analyzed within the relaxation time approximation (RTA). Since the RTA breaks down at temperatures low compared to the Debye temperature, this approximation prevents the study of an important class of high Debye temperature materials such as diamond, graphite, graphene and some other 2D materials. We present a full scattering matrix formalism that goes beyond the RTA approximation and obtain a Green's function solution for the linearized BTE, which leads to an explicit expression for the phonon distribution and temperature field produced by an arbitrary spatio-temporal distribution of heat sources in an unbounded medium. The presented formalism is capable of describing a wide range of phenomena, from heat dissipation by nanoscale hot spots to the propagation of second sound waves. We provide numerical results for graphene for a spatially sinusoidal heating profile and discuss the importance of using the full scattering matrix compared to the RTA.

cond-mat.mes-hall↗

arXiv2021

All-optical fluorescence blinking control in quantum dots with ultrafast mid-infrared pulses

Photoluminescence (PL) intermittency is a ubiquitous phenomenon detrimentally reducing the temporal emission intensity stability of single colloidal quantum dots (CQDs) and the emission quantum yield of their ensembles. Despite efforts for blinking reduction via chemical engineering of the QD architecture and its environment, blinking still poses barriers to the application of QDs, particularly in single-particle tracking in biology or in single-photon sources. Here, we demonstrate the first deterministic all-optical suppression of quantum dot blinking using a compound technique of visible and mid-infrared (MIR) excitation. We show that moderate-field ultrafast MIR pulses (5.5 $μ$m, 150 fs) can switch the emission from a charged, low quantum yield 'grey' trion state to the 'bright' exciton state in CdSe/CdS core-shell quantum dots resulting in a significant reduction of the QD intensity flicker. Quantum-tunneling simulations suggest that the MIR fields remove the excess charge from trions with reduced emission quantum yield to restore higher brightness exciton emission. Our approach can be integrated with existing single-particle tracking or super-resolution microscopy techniques without any modification to the sample and translates to other emitters presenting charging-induced PL intermittencies, such as single-photon emissive defects in diamond and two-dimensional materials.

cond-mat.mes-hall↗

arXiv2021

Hard X-ray Transient Grating Spectroscopy on Bismuth Germanate

Optical-domain Transient Grating (TG) spectroscopy is a versatile background-free four-wave-mixing technique used to probe vibrational, magnetic and electronic degrees of freedom in the time domain. The newly developed coherent X-ray Free Electron Laser sources allow its extension to the X-ray regime. Xrays offer multiple advantages for TG: their large penetration depth allows probing the bulk properties of materials, their element-specificity can address core-excited states, and their short wavelengths create excitation gratings with unprecedented momentum transfer and spatial resolution. We demonstrate for the first time TG excitation in the hard X-ray range at 7.1 keV. In Bismuth Germanate (BGO), the nonresonant TG excitation generates coherent optical phonons detected as a function of time by diffraction of an optical probe pulse. This experiment demonstrates the ability to probe bulk properties of materials and paves the way for ultrafast coherent four-wave-mixing techniques using X-ray probes and involving nanoscale TG spatial periods.

physics.optics↗

arXiv2021

High-velocity micro-projectile impact testing

High-velocity microparticle impacts are relevant to many fields from space exploration to additive manufacturing and can be used to help understand the physical and chemical behaviors of materials under extreme dynamic conditions. Recent advances in experimental techniques for single microparticle impacts have allowed fundamental investigations of dynamical responses of wide-ranging samples including soft materials, nano-composites, and metals, under strain rates up to 108 s-1. Here we review experimental methods for high-velocity impacts spanning 15 orders of magnitude in projectile mass and compare method performances. This review aims to present a comprehensive overview of high-velocity microparticle impact techniques to provide a reference for researchers in different materials testing fields and facilitate experimental design in dynamic testing for a wide range of impactor sizes, geometries, and velocities. Next, we review recent studies using the laser-induced particle impact test platform comprising target, projectile, and synergistic target-particle impact response, hence demonstrating the versatility of the method with applications in impact protection and additive manufacturing. We conclude by presenting the future perspectives in the field of high-velocity impact.

cond-mat.mtrl-sci↗

arXiv2020

Enantioselective Orientation of Chiral Molecules Induced by Terahertz Pulses with Twisted Polarization

Chirality and chiral molecules are key elements in modern chemical and biochemical industries. Individual addressing, and the eventual separation of chiral enantiomers has been and still is an important elusive task in molecular physics and chemistry, and a variety of methods has been introduced over the years to achieve this goal. Here, we theoretically demonstrate that a pair of cross-polarized THz pulses interacting with chiral molecules through their permanent dipole moments induces an enantioselective orientation of these molecules. This orientation persists for a long time, exceeding the duration of the THz pulses by several orders of magnitude, and its dependency on temperature and pulses' parameters is investigated. The persistent orientation may enhance the deflection of the molecules in inhomogeneous electromagnetic fields, potentially leading to viable separation techniques.

physics.optics↗

arXiv2020

Thermal transport in nanoporous holey silicon membranes investigated with optically-induced transient thermal gratings

In this study, we use the transient thermal grating optical technique \textemdash a non-contact, laser-based thermal metrology technique with intrinsically high accuracy \textemdash to investigate room-temperature phonon-mediated thermal transport in two nanoporous holey silicon membranes with limiting dimensions of 100 nm and 250 nm respectively. We compare the experimental results to ab initio calculations of phonon-mediated thermal transport according to the phonon Boltzmann transport equation (BTE) using two different computational techniques. We find that the calculations conducted within the Casimir framework, i.e. based on the BTE with the bulk phonon dispersion and diffuse scattering from surfaces, are in quantitative agreement with the experimental data, and thus conclude that this framework is adequate for describing phonon-mediated thermal transport through holey silicon membranes with feature sizes on the order of 100 nm.

cond-mat.mes-hall↗

arXiv2020

Nonlinear rotational spectroscopy reveals many-body interactions in water molecules

Because of their central importance in chemistry and biology, water molecules have been the subject of decades of intense spectroscopic investigations. Rotational spectroscopy of water vapor has yielded detailed information about the structure and dynamics of isolated water molecules as well as water dimers and clusters. Nonlinear rotational spectroscopy in the terahertz regime has been developed recently to investigate the rotational dynamics of linear and symmetric-top molecules whose rotational energy levels are regularly spaced, but it has not previously been applied to water or other lower-symmetry molecules with irregularly spaced levels. We report the use of recently developed two-dimensional terahertz rotational spectroscopy to observe high-order rotational coherences and correlations between rotational transitions that could not be observed previously. The results include two-quantum (2Q) peaks at frequencies that are shifted slightly from the sums of distinct rotational transitions on two molecules, which directly reveal the presence of previously unseen metastable water complexes with lifetimes of 100 ps or longer. Several such peaks observed at distinct 2Q frequencies indicate that the complexes have multiple preferred bimolecular geometries. Our results demonstrate sensitivity of rotational correlations measured in 2D THz spectroscopy to molecular interactions and complexation in the gas phase.

physics.chem-ph↗