RESUMO
Ever since its discovery1, the notion of the Berry phase has permeated all branches of physics and plays an important part in a variety of quantum phenomena2. However, so far all its realizations have been based on a continuous evolution of the quantum state, following a cyclic path. Here we introduce and demonstrate a conceptually new manifestation of the Berry phase in light-driven crystals, in which the electronic wavefunction accumulates a geometric phase during a discrete evolution between different bands, while preserving the coherence of the process. We experimentally reveal this phase by using a strong laser field to engineer an internal interferometer, induced during less than one cycle of the driving field, which maps the phase onto the emission of higher-order harmonics. Our work provides an opportunity for the study of geometric phases, leading to a variety of observations in light-driven topological phenomena and attosecond solid-state physics.
RESUMO
Symmetries are ubiquitous in condensed matter physics, playing an important role in the appearance of different phases of matter. Nonlinear light matter interactions serve as a coherent probe for resolving symmetries and symmetry breaking via their link to selection rules of the interaction. In the extreme nonlinear regime, high harmonic generation (HHG) spectroscopy offers a unique spectroscopic approach to study this link, probing the crystal spatial properties with high sensitivity while opening new paths for selection rules in the XUV regime. In this Letter we establish an advanced HHG polarimetry scheme, driven by a multicolor strong laser field, to observe the structural symmetries of solids and their interplay with the HHG selection rules. By controlling the crystal symmetries, we resolve nontrivial polarization states associated with new spectral features in the HHG spectrum. Our scheme opens new opportunities in resolving the symmetries of quantum materials, as well as ultrafast light driven symmetries in condensed matter systems.
