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Louis Primeau

Publications and source records attributed to Louis Primeau.

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Compact Spin-Charge Separated Neural Quantum States for Valence-Bond States

Neural-network quantum states (NQS) provide a flexible nonlinear representation of quantum many-body wavefunctions, but their efficiency depends sensitively on whether the architecture reflects the sign structure and constrained Hilbert space of the target state. In this work, we propose a solvable-point-guided strategy: design the architecture at an exactly solvable point where the correct local rules can be read off, then refine to the non-exact regime by enlarging only the kernel size and hidden dimension. The strategy is built from four physics-motivated designs: a stride-matched local-rule convolution, geometric pooling, a sign-resolving $\tanh(x^{2k+1})$ activation, and explicit spin-hole sector separation. We test this approach on quasi-one-dimensional valence-bond-solid (VBS) states and their doped soliton variants (sVBS), the exact ground states of a $t$-$J$-like model with a single mobile hole. In finite-size benchmarks, this architecture reaches high fidelity for the exact sVBS state with substantially fewer parameters than generic fully connected, convolutional, and transformer baselines tested under the same setup. For the spin sector, the learned local rule transfers from small to larger systems without retraining. Away from the solvable point, increasing kernel size and hidden dimension systematically improves accuracy, and the model shows approximately $L^2$ parameter scaling in the gapless regime for system size $L$, compared with approximately $L^4$ for matrix-product states in the same regime. Our work establishes a recipe for compact NQS in sign-structured, constrained Hilbert spaces and paves the pathway to physics-informed architectures for the broader $t$-$J$ and Hubbard families.

cond-mat.str-el

Non-covalent Interactions at cm$^{-1}$ Accuracy: Data Efficient Physics-Informed Distillation for Machine Learning Interatomic Potentials

Foundation models in atomistic machine learning encode interaction physics across diverse atomic environments, but whether that structure can be transferred when building specialist potentials at quantum-chemical accuracy remains open. Here we show that knowledge distillation from a pretrained universal machine-learning interatomic potential (MLIP), followed by coupled-cluster fine-tuning with single and double excitations and perturbative triples [CCSD(T)], transfers not only low-cost labels but a physically meaningful prior on interaction length scales, anisotropy, and the repulsive-dispersive balance, which CCSD(T) data then sharpens to quantum-chemical accuracy. For He--benzene, fine-tuning with 30% of the CCSD(T) data outperforms direct training using the full 80%; a 60% reduction in the high-fidelity compute budget. A symmetry-adapted perturbation theory (SAPT)-informed adaptive short-range/long-range architecture further lowers the validation MAE from 0.75 1/cm to 0.49 1/cm. Across a circumarene series of polycyclic aromatic hydrocarbons (PAHs), swapping the MLIP teacher under an otherwise identical pipeline changes the coronene error by an order of magnitude while leaving the larger PAHs stable, direct evidence that distillation transfers physical structure, not labels alone. Together, these results identify the choice of pretrained teacher as a primary design axis for data-efficient quantum-chemical-accuracy potentials, alongside architecture and training protocol.

physics.chem-ph

Angle-Resolved Berry Curvature via Nonlinear Hall Effect of Ballistic Electrons

Berry curvature fundamentally dictates the topological ground state, anomalous transport and optical properties of quantum materials. However, directly mapping its momentum-space distribution in real materials remains an outstanding experimental challenge. Here, we present an inverse method for reconstructing the abelian Berry curvature of a single band using angle-resolved measurements of the transverse conductance. Our inversion relies on a symmetry-constrained statistical model with two hyperparameters that can be inferred directly from the nonlinear Hall conductance, yielding a parameter-free inversion method. We demonstrate the feasibility of our method using simulated measurements of tight-binding models of WSe$_2$ and $ABC$-stacked trilayer graphene.

cond-mat.str-el

Modeling Quantum Geometry for Fractional Chern Insulators with unsupervised learning

Fractional Chern insulators (FCIs) in moire materials present a unique platform for exploring strongly correlated topological phases beyond the paradigm of ideal quantum geometry. While analytical approaches to FCIs and fractional quantum Hall states (FQHS) often rely on idealized Bloch wavefunctions, realistic moire models lack direct tunability of quantum metric and Berry curvature, limiting theoretical and numerical exploration. Here, we introduce an unsupervised machine learning framework to model interacting Hamiltonians directly through the distribution of single-particle form factors. Using a variational autoencoder (VAE), we show that unsupervised learning can not only distinguish FCI and non-FCI states, but also generate new form factors with distinct topological character, not present in the training set. This latent space enables the generation and interpolation of form factors for topological flatbands with Chern number $|C|=1$, enabling the discovery of unobserved many-body states such as charge density waves. Principal component analysis (PCA) further reveals that the dominant patterns in the form factors-reflecting correlations across the Brillouin zone-can be decomposed into components with approximately quantized Chern numbers, providing new insights into the global and topological structure of quantum geometry. Our results highlight the ability of machine learning to generalize and model topological quantum systems, paving the way for the inverse design of form factors with tailored quantum geometry and many-body phases in flatband materials.

cond-mat.str-el

Interaction-Driven Topological Transitions in Monolayer TaIrTe$_4$

Discovering materials that combine topological phenomena with correlated electron behavior is a central pursuit in quantum materials research. Monolayer TaIrTe$_4$ has recently emerged as a promising platform in this context, hosting robust quantum spin Hall insulator (QSHI) phases both within a single-particle gap and within a correlation-induced gap arising from van Hove singularities (vHSs), accessed via electrostatic doping. Its intrinsic monolayer nature offers exceptional tunability and the potential to realize a versatile array of interaction-driven topological phases. In this work, we combine theory and experiment to map the phase landscape of monolayer TaIrTe$_4$. Using Hartree-Fock calculations, we investigate the interaction-driven phase diagram near the vHSs under commensurate filling conditions. By systematically tuning the dielectric screening and strain, we uncover a rich set of ground states--including QSHI, trivial insulator, higher-order topological insulator, and metallic phase--among which are interaction-driven topological phase transitions. Experimentally, we perform both local and nonlocal transport measurements across a broad set of devices, which--due to unavoidable strain variations during fabrication-realize several phases consistent with theoretical predictions. Together, our results lay the groundwork for understanding correlation-driven topological phenomena in TaIrTe$_4$ and open new directions for engineering exotic quantum phases in low-dimensional materials beyond the limitations of moir\'e superlattices.

cond-mat.str-el

Direct observation of a photoinduced topological phase transition in Bi-doped (Pb,Sn)Se

Ultrafast photoexcitation offers a novel approach to manipulating quantum materials. One of the long-standing goals in this field is to achieve optical control over topological properties. However, the impact on their electronic structures, which host gapless surface states, has yet to be directly observed. Here, using time- and angle-resolved photoemission spectroscopy, we visualize the photo-induced evolution of the band structure in Biy(Pb1-xSnx)1-ySe(111) films from topological to trivial insulators. Following near-infrared ultrafast laser excitation, we observe that the topological surface state opens a substantial gap of up to 0.1 eV. Considering the topological phase diagram associated with lattice distortion and atomic displacement, we show that a uniaxial strain generated by the ultrafast optical pulse is sufficiently effective and strong for the observed topological phase transition. Our study highlights the potential of optical tuning of materials through laser excitation to control topological properties on ultrafast timescales.

cond-mat.mtrl-sci

Nonlinear photocurrent in quantum materials for broadband photodetection

Unlocking the vast potential of optical sensing technology has long been hindered by the challenges of achieving fast, sensitive, and broadband photodetection at ambient temperatures. In this review, we summarize recent progress in the study of nonlinear photocurrent in topological quantum materials, and its application in broadband photodetection without the use of p-n junction based semiconductor diodes. The intrinsic quadratic transverse current-input voltage relation is used to rectify the alternating electric field from incident radio, terahertz or infrared waves into a direct current, without a bias voltage and at zero magnetic field. We review novel photocurrents in several material systems, including topological Weyl semimetals, chiral crystals, ferroelectric materials, and low dimensional topological insulators. These quantum materials hold tremendous promise for broadband high-frequency rectification and photodetection, featuring substantial responsivity and detectivity.

cond-mat.mes-hall

SDEX: Monte Carlo Simulation of Stochastic Differential Equations on Memristor Crossbars

Here we present stochastic differential equations (SDEs) on a memristor crossbar, where the source of gaussian noise is derived from the random conductance due to ion drift in the devices during programming. We examine the effects of line resistance on the generation of normal random vectors, showing the skew and kurtosis are within acceptable bounds. We then show the implementation of a stochastic differential equation solver for the Black-Scholes SDE, and compare the distribution with the analytic solution. We determine that the random number generation works as intended, and calculate the energy cost of the simulation.

cs.ET