ABSTRACT
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.
ABSTRACT
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.
ABSTRACT
Interacting electrons in one dimension (1D) are governed by the Luttinger liquid (LL) theory in which excitations are fractionalized. Can a LL-like state emerge in a 2D system as a stable zero-temperature phase? This question is crucial in the study of non-Fermi liquids. A recent experiment identified twisted bilayer tungsten ditelluride (tWTe2) as a 2D host of LL-like physics at a few kelvins. Here we report evidence for a 2D anisotropic LL state down to 50 mK, spontaneously formed in tWTe2 with a twist angle of ~ 3o. While the system is metallic-like and nearly isotropic above 2 K, a dramatically enhanced electronic anisotropy develops in the millikelvin regime. In the anisotropic phase, we observe characteristics of a 2D LL phase including a power-law across-wire conductance and a zero-bias dip in the along-wire differential resistance. Our results represent a step forward in the search for stable LL physics beyond 1D.
ABSTRACT
Optical spectroscopy of quantum materials at ultralow temperatures is rarely explored, yet it may provide critical characterizations of quantum phases not possible using other approaches. We describe the development of a novel experimental platform that enables optical spectroscopic studies, together with standard electronic transport, of materials at millikelvin temperatures inside a dilution refrigerator. The instrument is capable of measuring both bulk crystals and micrometer-sized two-dimensional van der Waals materials and devices. We demonstrate its performance by implementing photocurrent-based Fourier transform infrared spectroscopy on a monolayer WTe2 device and a multilayer 1T-TaS2 crystal, with a spectral range available from the near-infrared to the terahertz regime and in magnetic fields up to 5 T. In the far-infrared regime, we achieve spectroscopic measurements at a base temperature as low as â¼43 mK and a sample electron temperature of â¼450 mK. Possible experiments and potential future upgrades of this versatile instrumental platform are envisioned.
