Ultrafast Transition from State-Blocking Dynamics to Electron Localization in Transition Metal β-Tungsten.

We describe an ultrafast transition of the electronic response of optically excited transition metal β-tungsten with few-femtosecond time resolution. The response moves from a regime where state filling of the excited carrier population around the Fermi level dominates towards localization of carriers onto the outer d orbitals. This is in contrast to previous measurements using ultrafast element-specific core-level spectroscopy enabled by attosecond transient absorption spectroscopy on transition metals such as titanium and around the transition metal atom in transition metal dichalchogenides MoTe_{2} and MoSe_{2}.

Ultrafast electron localization and screening in a transition metal dichalcogenide.

The coupling of light to electrical charge carriers in semiconductors is the foundation of many technological applications. Attosecond transient absorption spectroscopy measures simultaneously how excited electrons and the vacancies they leave behind dynamically react to the applied optical fields. In compound semiconductors, these dynamics can be probed via any of their atomic constituents with core-level transitions into valence and conduction band.

Water-window high harmonic generation with 0.8-µm and 2.2-µm OPCPAs at 100 kHz.

We compare the generation of high-order harmonics in the water window (283-543 eV) with 0.8-µm and 2.2-µm few-cycle lasers at a pulse repetition rate of 100 kHz.

High-power few-cycle near-infrared OPCPA for soft X-ray generation at 100 kHz.

We present a near-infrared optical parametric chirped-pulse amplifier (OPCPA) and soft X-ray (SXR) high-harmonic generation system. The OPCPA produces few-cycle pulses at a center wavelength of 800 nm and operates at a high repetition rate of 100 kHz. It is seeded by fully programmable amplitude and phase controlled ultra-broadband pulses from a Ti:sapphire oscillator.

Phase stabilization of an attosecond beamline combining two IR colors.

We present a phase-stabilized attosecond pump-probe beamline involving two separate infrared wavelengths for high-harmonic generation (HHG) and pump or probe. The output of a Ti:sapphire laser is partly used to generate attosecond pulses via HHG and partly to pump an optical parametric amplifier (OPA) that converts the primary Ti:sapphire radiation to a longer wavelength. The attosecond pulse and down-converted infrared are recombined after a more than 20-m-long Mach-Zehnder interferometer that spans across two laboratories and separate optical tables.

Ultrafast nuclear dynamics of the acetylene cation CH and its impact on the infrared probe pulse induced C-H bond breaking efficiency.

The ultrafast nuclear dynamics of the acetylene cation C2H2+ following photoionization of the neutral molecule is investigated using an extreme-ultraviolet pump/infrared probe setup. The observed modulation of the C2H+ fragment ion yield with pump-probe delay is related to structural changes induced by the extreme-ultraviolet pump pulse taking place on the femtosecond timescale. High-level simulations suggest that the trans-bending and C-C bond stretching motion of the C2H2+ cation govern the observed interaction with the infrared pulse.

Reduction of laser-intensity-correlated noise in high-harmonic generation.

We present a scheme for correcting the spectral fluctuations of high-harmonic radiation. We show that the fluctuations of the extreme-ultraviolet (XUV) spectral power density can be predicted solely by monitoring the generating laser pulses; this method is in contrast with traditional balanced detection used in optical spectroscopy, where a replica of the signal is monitored. Such possibility emerges from a detailed investigation of high-harmonic generation (HHG) noise.

High-power OPCPA generating 1.7 cycle pulses at 2.5 µm.

We present a high-power mid-infrared (mid-IR) optical parametric chirped-pulse amplifier (OPCPA) generating 14.4 fs pulses centered at 2.5 µm with an average power of 12.

Decoupling phase-matching bandwidth and interaction geometry using non-collinear quasi-phase-matching gratings.

In optical parametric amplification (OPA) of broadband pulses, a non-collinear angle between the interacting waves is typically introduced in order to achieve broadband phase-matching. Consequently, bandwidth and beam geometry are closely linked. This coupling restricts the geometrical layout of an OPA system.

Anisotropic photoemission time delays close to a Fano resonance.

Electron correlation and multielectron effects are fundamental interactions that govern many physical and chemical processes in atomic, molecular and solid state systems. The process of autoionization, induced by resonant excitation of electrons into discrete states present in the spectral continuum of atomic and molecular targets, is mediated by electron correlation. Here we investigate the attosecond photoemission dynamics in argon in the 20-40 eV spectral range, in the vicinity of the 3snp autoionizing resonances.

Strong field transient manipulation of electronic states and bands.

In the present review, laser fields are so strong that they become part of the electronic potential, and sometimes even dominate the Coulomb contribution. This manipulation of atomic potentials and of the associated states and bands finds fascinating applications in gases and solids, both in the bulk and at the surface. We present some recent spectacular examples obtained within the NCCR MUST in Switzerland.

Photoemission and photoionization time delays and rates.

Ionization and, in particular, ionization through the interaction with light play an important role in fundamental processes in physics, chemistry, and biology. In recent years, we have seen tremendous advances in our ability to measure the dynamics of photo-induced ionization in various systems in the gas, liquid, or solid phase. In this review, we will define the parameters used for quantifying these dynamics.

Erratum: Resonance Effects in Photoemission Time Delays [Phys. Rev. Lett. 115, 133001 (2015)].

This corrects the article DOI: 10.1103/PhysRevLett.115.

Gouy phase shift for annular beam profiles in attosecond experiments.

Attosecond pump-probe measurements are typically performed by combining attosecond pulses with more intense femtosecond, phase-locked infrared (IR) pulses because of the low average photon flux of attosecond light sources based on high-harmonic generation (HHG). Furthermore, the strong absorption of materials at the extreme ultraviolet (XUV) wavelengths of the attosecond pulses typically prevents the use of transmissive optics. As a result, pump and probe beams are typically recombined geometrically with a center-hole mirror that reflects the larger IR beam and transmits the smaller XUV, which leads to an annular beam profile of the IR.

Comparison of attosecond streaking and RABBITT.

Recent progress in the generation of ultra-short laser pulses has enabled the measurement of photoionization time delays with attosecond precision. For single photoemission time delays the most common techniques are based on attosecond streaking and the reconstruction of attosecond beating by interference of two-photon transitions (RABBITT). These are pump-probe techniques employing an extreme-ultraviolet (XUV) single attosecond pump pulse for streaking or an attosecond pump pulse train for RABBITT, and a phase-locked infrared (IR) probe pulse.

Delayed electron emission in strong-field driven tunnelling from a metallic nanotip in the multi-electron regime.

Illuminating a nano-sized metallic tip with ultrashort laser pulses leads to the emission of electrons due to multiphoton excitations. As optical fields become stronger, tunnelling emission directly from the Fermi level becomes prevalent. This can generate coherent electron waves in vacuum leading to a variety of attosecond phenomena.

Attosecond dynamical Franz-Keldysh effect in polycrystalline diamond.

Short, intense laser pulses can be used to access the transition regime between classical and quantum optical responses in dielectrics. In this regime, the relative roles of inter- and intraband light-driven electronic transitions remain uncertain. We applied attosecond transient absorption spectroscopy to investigate the interaction between polycrystalline diamond and a few-femtosecond infrared pulse with intensity below the critical intensity of optical breakdown.

Frequency-domain nonlinear optics in two-dimensionally patterned quasi-phase-matching media.

Advances in the amplification and manipulation of ultrashort laser pulses have led to revolutions in several areas. Examples include chirped pulse amplification for generating high peak-power lasers, power-scalable amplification techniques, pulse shaping via modulation of spatially-dispersed laser pulses, and efficient frequency-mixing in quasi-phase-matched nonlinear crystals to access new spectral regions. In this work, we introduce and demonstrate a new platform for nonlinear optics which has the potential to combine these separate functionalities (pulse amplification, frequency transfer, and pulse shaping) into a single monolithic device that is bandwidth- and power-scalable.

Ultrafast Relaxation Dynamics of the Ethylene Cation C(2)H(4)+.

We present a combined experimental and computational study of the relaxation dynamics of the ethylene cation. In the experiment, we apply an extreme-ultraviolet-pump/infrared-probe scheme that permits us to resolve time scales on the order of 10 fs. The photoionization of ethylene followed by an infrared (IR) probe pulse leads to a rich structure in the fragment ion yields reflecting the fast response of the molecule and its nuclei.

Ptychographic reconstruction of attosecond pulses.

We demonstrate a new attosecond pulse reconstruction modality which uses an algorithm that is derived from ptychography. In contrast to other methods, energy and delay sampling are not correlated, and as a result, the number of electron spectra to record is considerably smaller. Together with the robust algorithm, this leads to a more precise and fast convergence of the reconstruction.

Light-Matter Interaction at Surfaces in the Spatiotemporal Limit of Macroscopic Models.

What is the spatiotemporal limit of a macroscopic model that describes the optoelectronic interaction at the interface between different media? This fundamental question has become relevant for time-dependent photoemission from solid surfaces using probes that resolve attosecond electron dynamics on an atomic length scale. We address this fundamental question by investigating how ultrafast electron screening affects the infrared field distribution for a noble metal such as Cu(111) at the solid-vacuum interface. Attosecond photoemission delay measurements performed at different angles of incidence of the light allow us to study the detailed spatiotemporal dependence of the electromagnetic field distribution.

Resonance Effects in Photoemission Time Delays.

We present measurements of single-photon ionization time delays between the outermost valence electrons of argon and neon using a coincidence detection technique that allows for the simultaneous measurement of both species under identical conditions. The analysis of the measured traces reveals energy-dependent time delays of a few tens of attoseconds with high energy resolution. In contrast to photoelectrons ejected through tunneling, single-photon ionization can be well described in the framework of Wigner time delays.

Semi-classical approach to compute RABBITT traces in multi-dimensional complex field distributions.

We present a semi-classical model to calculate RABBITT (Reconstruction of Attosecond Beating By Interference of Two-photon Transitions) traces in the presence of a reference infrared field with a complex two-dimensional (2D) spatial distribution. The evolution of the electron spectra as a function of the pump-probe delay is evaluated starting from the solution of the classical equation of motion and incorporating the quantum phase acquired by the electron during the interaction with the infrared field. The total response to an attosecond pulse train is then evaluated by a coherent sum of the contributions generated by each individual attosecond pulse in the train.

Breakdown of the dipole approximation in strong-field ionization.

We report the breakdown of the electric dipole approximation in the long-wavelength limit in strong-field ionization with linearly polarized few-cycle mid-infrared laser pulses at intensities on the order of 10¹³ W/cm². Photoelectron momentum distributions were recorded by velocity map imaging and projected onto the beam propagation axis. We observe an increasing shift of the peak of this projection opposite to the beam propagation direction with increasing laser intensities.

Revealing the time-dependent polarization of ultrashort pulses with sub-cycle resolution.

We report on the first experiments characterizing the complete time-dependent 2D vector potential of a few-cycle laser pulse. The instantaneous amplitude and orientation of the electric field is determined with sub-cycle resolution, directly giving access to the polarization state of the pulse at any instant in time. This is achieved by performing an attosecond streaking experiment using a reaction microscope, where the full pulse characterization is performed directly in the target region.