Georg Wachter

Electron rescattering at metal nanotips induced by ultrashort laser pulses

We report on the first investigation of plateau and cut-off structures in photoelectron spectra from nano-scale metal tips interacting with few-cycle near-infrared laser pulses. These hallmarks of electron rescattering, well-known from atom-laser interaction in the strong-field regime, appear at remarkably low laser intensities with nominal Keldysh parameters of the order of

Interaction of ultrashort laser pulses with metal nanotips: a model system for strong-field phenomena

\gtrsim 10

Ab initio simulation of electrical currents induced by ultrafast laser excitation of dielectric materials.

. Quantum and quasi-classical simulations reveal that a large field enhancement near the tip and the increased backscattering probability at a solid-state target play a key role. Plateau electrons are by an order of magnitude more abundant than in comparable atomic spectra, reflecting the high density of target atoms at the surface. The position of the cut-off serves as an in-situ probe for the locally enhanced electric field at the tip apex.

Large optical field enhancement for nanotips with large opening angles

We discuss the interaction of ultrashort near-infrared laser pulses with sharp metal tips at moderate nominal intensities (I0 10 11 Wcm 2 ). As external electric fields are strongly enhanced at such tips (enhancement factor 10) our system turns out to be an ideal miniature laboratory to investigate strong-field effects at solid surfaces. We analyse the electron-energy spectra as a function of the strength of the laser field and the static extraction field and present an intuitive model for their interpretation. The size of the effective field acting on the metal electrons can be determined from the electron spectra. The latter are also reproduced by time-dependent density functional theory (TDDFT) simulations.

Ab initio multiscale simulation of high-order harmonic generation in solids

We theoretically investigate the generation of ultrafast currents in insulators induced by strong few-cycle laser pulses. Ab initio simulations based on time-dependent density functional theory give insight into the atomic-scale properties of the induced current signifying a femtosecond-scale insulator-metal transition. We observe the transition from nonlinear polarization currents during the laser pulse at low intensities to tunnelinglike excitation into the conduction band at higher laser intensities. At high intensities, the current persists after the conclusion of the laser pulse considered to be the precursor of the dielectric breakdown on the femtosecond scale. We show that the transferred charge sensitively depends on the orientation of the polarization axis relative to the crystal axis, suggesting that the induced charge separation reflects the anisotropic electronic structure. We find good agreement with very recent experimental data on the intensity and carrier-envelope phase dependence [A. Schiffrin et al., Nature (London) 493, 70 (2013).

Observation of molecular dipole excitations by attosecond self-streaking

We theoretically investigate the dependence of the enhancement of optical near-fields at nanometric tips on the shape, size, and material of the tip. We confirm a strong dependence of the field enhancement factor on the radius of curvature. In addition, we find a surprisingly strong increase of field enhancement with increasing opening angle of the nanotips. For gold and tungsten nanotips in the experimentally relevant parameter range (radius of curvature

Controlling ultrafast currents by the nonlinear photogalvanic effect

\geq 5\,

Modelling surface restructuring by slow highly charged ions

nm at

Geometrical model fitting for interferometric data: GEM-FIND

800\,

Simulation of High Harmonic Generation in Solids

nm laser wavelength), we obtain field enhancement factors of up to