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P. Baum

Publications and source records attributed to P. Baum.

8 recordsLinked to original sources

Quantum tomography of free electrons

Determining the quantum state of a given quantum-mechanical system is a fundamental task in physics. Quantum-state tomography has been pivotal for establishing quantum optics [1-4] and for revealing the properties of bound charges in materials [5-7]. An emerging other object for studying and utilizing quantum effects are free electrons, elementary particles that are central to high-resolution microscopy [8,9], electron-based quantum optics [10-17], ul-trafast electron microscopy [18-24] and particle accelerators [25-27]. However, free electrons are intrinsically incoherent, and we lack a broadly applicable method to measure and control their quantum state beyond special cases with discrete energy sidebands [28,29]. Here, we report a universal approach to measure arbitrary free-electron quantum states in continuous variables. Two monochromatic but spectrally shifted laser waves produce interfering quan-tum paths that directly reveal the density matrix and thus all essential properties of the pure wavepackets, the ensemble, and their interlinks. As a first application, we show how the quantum state of a single electron is modified by many-body Coulomb interactions of a sur-rounding electron gas. The reported concepts and results provide insight into otherwise hid-den correlations in electron beams and enable the controlled optimization of exceptional quantum states for free-electron quantum optics or quantum electron microscopy.

quant-ph

Electron modulation and ultrafast near-field imaging with vectorial laser fields

Controlled interaction of laser light with electron beams is fundamental for ultrafast electron microscopy and electron-based quantum optics, yet their direct coupling is forbidden in free space. Here we use longitudinally polarized light at a thin membrane and show that the emerging focal fields can modulate the electron beam in a direct, coherent and linear way, without the need for nanostructured materials or slanted interaction geometries. Also, we use vectorial polarizations to excite and probe three-dimensional nanophotonic near-fields in metallic mesocrystals by coherent electron energy gain and loss. We find that longitudinal electric fields excite axial near-fields in a direct way while longitudinal magnetic fields excite oscillating ring currents via azimuthal electric fields. These possibilities enable tilt-free, collinear generation of attosecond electron pulses or free-electron qubits and provide novel imaging modes in ultrafast electron microscopy and metamaterial tomography.

physics.optics

Deciphering the dynamics of the light-induced phase transition in VO$_2$

Vanadium dioxide (VO$_2$) is central in the study of ultrafast photoinduced insulator-to-metal phase transitions in strongly correlated materials, and a primary candidate for next-generation light-driven devices. However, the physical mechanism underlying its phase transition remains unresolved. Here, we use single-cycle light transients to perform phase-resolved ultrafast spectroscopy on VO$_2$ crystals. Our experiments reveal two processes: a structural transformation from the insulating monoclinic M1-VO$_2$ phase to the excited metallic rutile R*-VO$_2$ phase, followed by electron thermalization and relaxation dynamics intrinsic to the newly formed excited metallic phase.

cond-mat.str-el

Stronger femtosecond excitation causes slower electron-phonon coupling in silicon

Electron-hole pairs in semiconductors are essential for solar cells and fast electronic circuitry, but the competition between carrier transport and relaxation into heat limits the efficiency and speed. Here we use ultrafast electron diffraction with terahertz pulse compression to measure the electron-phonon decay rate in single-crystal silicon as a function of laser excitation strength. We find that the excited electrons relax slower into phonons for higher carrier densities. The electron-phonon scattering rate changes in a nonlinear way from 400 fs at ~$2 \times 10^{20} \text{ cm}^{-3}$ to 1.2 ps at ~$4 \times 10^{20} \text{ cm}^{-3}$. These results indicate that a hot electron gas quenches the scattering into phonons in a temperature-dependent way. Ultrafast electronic circuitry of silicon therefore should work faster and provide higher bandwidths at lower carrier densities.

cond-mat.mtrl-sci

Electron matter waves with internal torque

Angular momentum and torque are important principles for basic and applied physics on any spatial scales, for example, in elementary particles, cold gases, optical tweezers, quantum information technology, metamaterials, gyroscopes or astrophysical entities. Investigating or controlling angular momentum in atoms or sub-atomic structures requires torque on femtosecond and picometer scales, far below the capabilities of laser light. Here we shape the electrons in an electron microscope into wave packets with a time-dependent chirality and internal torque. We intersect the electron beam with chiral laser light to create discrete energy sidebands by multiple helical photon absorptions that create a correlation between orbital angular momentum and kinetic energy. Dispersion of these partial waves due to the electron rest mass then converts each single electron into a wave function with internal torque. Under our control, a left-handed matter wave becomes right-handed in femtosecond times. Such quantum objects will facilitate research on angular momentum and chirality on atomic and sub-atomic scales.

physics.optics

Comment on 'Attosecond electron microscopy and diffraction'

A recent paper by Hui et al. (Ref. [1], Sci. Adv. 10, eadp5805 (2024)) claims the demonstration of 'Attosecond electron microscopy and diffraction' with laser-gated electron pulses. In this comment, we point out a series of physical and technical inconsistencies of the experiment and results. Beyond failing to show any microscopy, the reported concept does not produce properly gated electrons. Furthermore, the noise and signal levels of the presented data are statistically and quantitatively incompatible with the work's interpretation and attosecond dynamics in graphite. These inconsistencies render the claims and conclusions of Ref. [1] unsubstantiated and suggest that the data primarily show an interferometric artifact.

cond-mat.mtrl-sci

Terahertz control in a transmission electron microscope

Ultrafast electron microscopy provides a movie-like access to structural dynamics of materials in space and time, but fundamental atomic motions or electron dynamics are, so far, too quick to be resolved. Here we report the all-optical control, compression and characterization of electron pulses in a transmission electron microscope by the single optical cycles of laser-generated terahertz light. This concept provides isolated electron pulses and merges the spatial resolution of a transmission electron microscope with the temporal resolution that is offered by a single cycle of laser light. Central to these achievements is a perforated parallel-plate metallic waveguide in which transverse velocity mismatch and magnetic forces are mitigated by electrically constructive and magnetically destructive interferences of incoming and reflected terahertz half-cycles from a displaced waveguide termination. Measurements of spatial chirp via energy-filtered imaging reveal flat pulses with no transversal deflection or temporal aberrations at the specimen. We also report the all-optical control of multi-electron states and discover a substantial two-electron and three-electron anti-correlation in the time domain. These results open up the possibility to visualize atomic and electronic motions together with their quantum correlations on fundamental dimensions in space and time.

physics.optics

Polarized phonons carry the missing angular momentum in femtosecond demagnetization

Magnetic phenomena are ubiquitous in our surroundings and indispensable for modern science and technology, but it is notoriously difficult to change the magnetic order of a material in a rapid way. However, if a thin nickel film is subjected to ultrashort laser pulses, it can lose its magnetic order almost completely within merely femtosecond times. This phenomenon, in the meantime also observed in many other materials, has connected magnetism with femtosecond optics in an efficient, ultrafast and complex way, offering opportunities for rapid information processing or ultrafast spintronics at frequencies approaching those of light. Consequently, the physics of ultrafast demagnetization is central to modern material research, but a crucial question has remained elusive: If a material loses its magnetization within only femtoseconds, where is the missing angular momentum in such short time? Here we use ultrafast electron diffraction to reveal in nickel an almost instantaneous, long-lasting, non-equilibrium population of anisotropic high-frequency phonons that appear as quickly as the magnetic order is lost. The anisotropy plane is perpendicular to the direction of the initial magnetization and the atomic oscillation amplitude is 2 pm. We explain these observations by means of circularly polarized phonons that quickly absorb the missing angular momentum of the spin system before the slower onset of a macroscopic sample rotation. The time that is needed for demagnetization is related to the time it takes to accelerate the atoms. These results provide an atomistic picture of ultrafast demagnetization under adherence to all conservation laws but also demonstrate the general importance of polarized phonons for non-equilibrium dynamics and provide innovative ways for controlling materials on atomic dimensions.

cond-mat.mtrl-sci