Pengjie Wang

Nanophotonic quantum memory is a vital component for scalable quantum information processing for quantum computing, networking, and sensing applications. We store single-photon-level telecom-band optical pulses for more than 1 μs using an atomic frequency comb in erbium-doped thin-film lithium niobate (TFLN), well beyond what is practically feasible via propagation in even the best nanophotonic devices due to propagation losses. We verify the quantum nature of this storage by demonstrating the phase coherence and subsingle-photon noise upon retrieval. We also show the flexibility of our platform by storing up to 20 temporal modes and demonstrating an acceptance bandwidth of up to 2.2 GHz. These results establish erbium-doped TFLN as a practical platform for on-chip quantum memory at telecom wavelengths, a key missing element for photonic quantum computing and quantum networking.

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 ~ 3^o. 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.

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 ∼43 mK and a sample electron temperature of ∼450 mK. Possible experiments and potential future upgrades of this versatile instrumental platform are envisioned.

Two-dimensional (2D) material research is rapidly evolving to broaden the spectrum of emergent 2D systems. Here, we review recent advances in the theory, synthesis, characterization, device, and quantum physics of 2D materials and their heterostructures. First, we shed insight into modeling of defects and intercalants, focusing on their formation pathways and strategic functionalities. We also review machine learning for synthesis and sensing applications of 2D materials. In addition, we highlight important development in the synthesis, processing, and characterization of various 2D materials (e.g., MXnenes, magnetic compounds, epitaxial layers, low-symmetry crystals, etc.) and discuss oxidation and strain gradient engineering in 2D materials. Next, we discuss the optical and phonon properties of 2D materials controlled by material inhomogeneity and give examples of multidimensional imaging and biosensing equipped with machine learning analysis based on 2D platforms. We then provide updates on mix-dimensional heterostructures using 2D building blocks for next-generation logic/memory devices and the quantum anomalous Hall devices of high-quality magnetic topological insulators, followed by advances in small twist-angle homojunctions and their exciting quantum transport. Finally, we provide the perspectives and future work on several topics mentioned in this review.

The Luttinger liquid (LL) model of one-dimensional (1D) electronic systems provides a powerful tool for understanding strongly correlated physics, including phenomena such as spin–charge separation¹. Substantial theoretical efforts have attempted to extend the LL phenomenology to two dimensions, especially in models of closely packed arrays of 1D quantum wires^{2,3,4,5,6,7,8,9,10,11,12,13}, each being described as a LL. Such coupled-wire models have been successfully used to construct two-dimensional (2D) anisotropic non-Fermi liquids^2,3,4,5,6, quantum Hall states^7,8,9, topological phases^10,11 and quantum spin liquids^12,13. However, an experimental demonstration of high-quality arrays of 1D LLs suitable for realizing these models remains absent. Here we report the experimental realization of 2D arrays of 1D LLs with crystalline quality in a moiré superlattice made of twisted bilayer tungsten ditelluride (tWTe₂). Originating from the anisotropic lattice of the monolayer, the moiré pattern of tWTe₂ hosts identical, parallel 1D electronic channels, separated by a fixed nanoscale distance, which is tuneable by the interlayer twist angle. At a twist angle of approximately 5 degrees, we find that hole-doped tWTe₂ exhibits exceptionally large transport anisotropy with a resistance ratio of around 1,000 between two orthogonal in-plane directions. The across-wire conductance exhibits power-law scaling behaviours, consistent with the formation of a 2D anisotropic phase that resembles an array of LLs. Our results open the door for realizing a variety of correlated and topological quantum phases based on coupled-wire models and LL physics.

The phenomenon of group motion is common in nature, ranging from the schools of fish, birds and insects, to avalanches, landslides and sand drift. If we treat objects as collectively moving particles, such phenomena can be studied from a physical point of view, and the research on many-body systems has proved that marvelous effects can arise from the simplest individuals. The motion of numerous individuals presents different dynamic phases related to the ordering of the system. However, it is usually difficult to study the dynamic ordering and its transitions through experiments. Electron bubble states formed in a two-dimensional electron gas, as a type of electron solids, can be driven by an external electric field and provide a platform to study the dynamic collective behaviors. Here, we demonstrate that the noise spectrum is a powerful method to investigate the dynamics of bubble states. We observed not only the phenomena of dynamically ordered and disordered structures, but also unexpected alternations between them. Our results show that a dissipative system can convert between chaotic structures and ordered structures when tuning global parameters, which is concealed in conventional transport measurements of resistance or conductance. Moreover, charging the objects to study the electrical noise spectrum in collective motions can be an additional approach to revealing dynamic ordering transitions.