Quantum phase transitions are a ubiquitous many-body phenomenon that occurs in a wide range of physical systems, including superconductors, quantum spin liquids, and topological materials. However, investigations of quantum critical systems also repr
esent one of the most challenging problems in physics, since highly correlated many-body systems rarely allow for an analytic and tractable description. Here we present a Lee-Yang theory of quantum phase transitions including a method to determine quantum critical points which readily can be implemented within the tensor network formalism and even in realistic experimental setups. We apply our method to a quantum Ising chain and the anisotropic quantum Heisenberg model and show how the critical behavior can be predicted by calculating or measuring the high cumulants of properly defined operators. Our approach provides a powerful formalism to analyze quantum phase transitions using tensor networks, and it paves the way for systematic investigations of quantum criticality in two-dimensional systems.
Quantum dots are one of the paradigmatic solid-state systems for quantum engineering, providing an outstanding tunability to explore fundamental quantum phenomena. Here we show that non-Hermitian many-body topological modes can be realized in a quant
um dot chain by utilizing a gate-tunable modulation of dissipation, and they emerge purely because of the non-Hermiticity. By exactly solving the non-Hermitian interacting description both with exact diagonalization and tensor-networks, we demonstrate that these topological modes are robust even in the presence strong interactions, leading to a strongly correlated topological many-particle state. Our results put forward quantum dot arrays as a platform for engineering non-Hermitian many-body topological modes, and highlight the resilience of non-Hermitian topology to electronic interactions.
Van der Waals materials can be easily combined in lateral and vertical heterostructures, providing an outstanding platform to engineer elusive quantum states of matter. However, a critical problem in material science is to establish tangible links be
tween real materials properties and terms that can be cooked up on the model Hamiltonian level to realize different exotic phenomena. Our review aims to do precisely this: we first discuss, in a way accessible to the materials community, what ingredients need to be included in the hybrid quantum materials recipe, and second, we elaborate on the specific materials that would possess the necessary qualities. We will review the well-established procedures for realizing 2D topological superconductors, quantum spin-liquids and flat bands systems, emphasizing the connection between well-known model Hamiltonians and real compounds. We will use the most recent experimental results to illustrate the power of the designer approach.
Van der Waals (VdW) materials have opened new directions in the study of low dimensional magnetism. A largely unexplored arena is the intrinsic tuning of VdW magnets toward new ground-states. The chromium trihalides provided the first such example wi
th a change of inter-layer magnetic coupling emerging upon exfoliation. Here, we take a different approach to engineer new ground-states, not by exfoliation, but by tuning the spin-orbit coupling (SOC) of the non-magnetic ligand atoms (Cl,Br,I). We synthesize a three-halide series, CrCl$_{3-x-y}$Br$_{x}$I$_{y}$, and map their magnetic properties as a function of Cl, Br, and I content. The resulting triangular phase diagrams unveil a frustrated regime near CrCl$_{3}$. First-principles calculations confirm that the frustration is driven by a competition between the chromium and halide SOCs. Furthermore, we reveal a field-induced change of inter-layer coupling in the bulk of CrCl$_{3-x-y}$Br$_{x}$I$_{y}$ crystals at the same field as in the exfoliation experiments.
Atomic defects have a significant impact in the low-energy properties of graphene systems. By means of first-principles calculations and tight-binding models we provide evidence that chemical impurities modify both the normal and the superconducting
states of twisted bilayer graphene. A single hydrogen atom attached to the bilayer surface yields a triple-point crossing, whereas self-doping and three-fold symmetry-breaking are created by a vacant site. Both types of defects lead to time-reversal symmetry-breaking and the creation of local magnetic moments. Hydrogen-induced magnetism is found to exist also at the doping levels where superconductivity appears in magic angle graphene superlattices. As a result, the coexistence of superconducting order and defect-induced magnetism yields in-gap Yu-Shiba-Rusinov excitations in magic angle twisted bilayer graphene.
Two-dimensional semiconducting materials are particularly appealing for many applications. Although theory predicts a large number of two-dimensional materials, experimentally only a few of these materials have been identified and characterized compr
ehensively in the ultrathin limit. Lead iodide, which belongs to the transition metal halides family and has a direct bandgap in the visible spectrum, has been known for a long time and has been well characterized in its bulk form. Nevertheless, studies of this material in the nanometer thickness regime are rather scarce. In this article we demonstrate an easy way to synthesize ultrathin, highly crystalline flakes of PbI2 by precipitation from a solution in water. We thoroughly characterize the produced thin flakes with different techniques ranging from optical and Raman spectros-copy to temperature-dependent photoluminescence and electron microscopy. We compare the results to ab initio calculations of the band structure of the material. Finally, we fabricate photodetectors based on PbI2 and study their optoelectronic properties.
