Magnon-induced phononic Chern insulator

From butterfly wings to remnants of nuclear detonation, aperiodic order repeatedly emerges in nature, often exhibiting reduced sensitivity to boundaries and symmetry constraints. Inspired by this principle, a paradigm shift is introduced in nanomechanical resonator design from periodic to aperiodic structures, focusing on a special class: quasicrystals (QCs). Although soft clamping enabled by phononic stopbands has become a central strategy for achieving high-$Q_m$ nanomechanical resonators, its practical realization has been largely confined to periodic phononic crystals, where band structure engineering is well established. The potential of aperiodic architectures, however, has remained largely unexplored, owing to their intrinsic complexity and the lack of systematic approaches to identifying and exploiting stopband behavior. Here we demonstrate that soft clamping can be realized in quasicrystal architectures and that high-$Q_m$ nanomechanical resonators can be systematically predicted through a data-driven design framework. As a representative demonstration, the 12-fold QC-based resonator obtained numerically a quality factor $Q_m \sim 10^7$ and an effective mass of sub-nanograms at MHz frequencies, corresponding to an exceptional force sensitivity of $26.4$~aN/$\sqrt{\text{Hz}}$ compared to previous 2D phononic crystals. These results establish QCs as a robust platform for next-generation nanomechanical resonators and open a new design regime beyond periodic order.

A two-dimensional electron gas in a uniform neutralizing background forms a triangular Wigner crystal at low density. In a strongly mass-asymmetric electron-hole bilayer, localized heavy holes instead provide a nonuniform positive background that supports an electron crystal at densities two orders of magnitude higher than for a homogeneous electron gas in the same material. Here we show that correlated mobile electrons can overturn the preference for triangular order, stabilizing a honeycomb electron-hole crystal. Using the powerful real-space neural-network variational Monte Carlo in the Born-Oppenheimer limit with fixed holes, we find that increasing the density drives a transition from a triangular electron-hole crystal to a honeycomb crystal, which eventually melts into itinerant electrons coexisting with the honeycomb or the triangular hole lattice at fixed interlayer separation. Relative to triangular order, honeycomb order emerges when gains in electronic kinetic energy and electron-hole attraction outweigh its higher intralayer Coulomb repulsion, a threshold never reached in the rigid point-dipole model. Moreover, the honeycomb hole lattice supports paramagnetic, antiferromagnetic, and stripe-ordered spin states. Complex polarization indicates a metal-insulator transition, while the states on the honeycomb hole lattice are consistent with a stripe-ordered Dirac semimetal and paramagnetic or antiferromagnetic Mott insulators via mapping to the half-filled Hubbard model. We further propose a BLG/hBN/WS$_2$-WSe$_2$ heterostructure as a platform for the predicted honeycomb crystal, at an experimentally feasible density $n\sim10^{11}~\text{cm}^{-2}$.

Discovering materials that must simultaneously satisfy multiple competing constraints remains a central challenge in computational materials design, particularly in data-scarce regimes where conventional data-driven approaches are least effective. Magnetic insulators represent a stringent example: the electronic conditions that favor magnetic order often also promote metallicity, while insulating behavior suppresses the interactions that stabilize magnetism. As a result, experimentally viable magnetic insulators are rare and difficult to identify through conventional screening. Here, we introduce MagMatLLM, a constraint-guided generative discovery framework that integrates language-model-based crystal generation with evolutionary selection, surrogate screening, and first-principles validation to target simultaneous stability, magnetism, and insulating behavior. Unlike stability-first approaches, the framework enforces functional constraints during generation and selection, steering the search toward sparsely populated regions of materials space defined by competing physical requirements. Using this workflow, we identify twelve previously unreported candidate magnetic insulators, including Tm$_4$Co$_2$Cr$_2$O$_{12}$ and Cr$_4$Nb$_2$O$_{12}$. Of these, ten are dynamically stable by phonon analysis and exhibit finite band gaps and nonzero magnetic moments in spin-polarized density functional theory calculations. Beyond the specific compounds identified here, this work establishes a general constraint-guided paradigm for multi-objective materials discovery in sparse chemical spaces and provides a transferable strategy for the design of quantum materials under competing physical constraints.