Search arXiv⌕ Search

arXiv · 2609.37058

Linear-Scaling Quantum Transport from Machine-Learning Density Functional Theory Hamiltonians

Abstract

Quantum transport simulations that combine density functional theory (DFT) with the nonequilibrium Green's function formalism (DFT-NEGF) are important to modern technology, yet their unfavorable scaling has long confined predictive simulations to small, idealized systems far below the ten-thousand-atom scale of realistic devices. Here, we introduce HamGNN-NEGF, a linear-scaling framework with DFT-level fidelity. An E(3)-equivariant graph neural network trained on conventional DFT Hamiltonians of small structures predicts Hamiltonians for large devices, avoiding costly DFT-NEGF training data. The predicted Hamiltonians are integrated with DFT-derived electrode self-energies, a nonorthogonal kernel polynomial method for Fermi-level determination, and a recursive Green's function algorithm, yielding a computational cost that scales linearly with device length at fixed cross section. Even for devices containing fewer than 500 atoms, HamGNN-NEGF achieves speedups exceeding three orders of magnitude over fully self-consistent DFT-NEGF, with the advantage increasing further with system size. Benchmarks on pristine Pt-Si-Pt, doped Pt-Si:P-Pt, and Pt-molecule-Pt junctions demonstrate meV-level Hamiltonian accuracy, faithful transmission spectra, and predictive simulations beyond 10,000 atoms. Eliminating transport self-consistency also enables hybrid functionals such as HSE06 without additional NEGF overhead, while a zero-bias Hamiltonian approximation extends the framework to finite-bias transport in weakly nonlinear regimes. HamGNN-NEGF thus bridges first-principles accuracy and device-scale simulation, providing a practical route toward predictive modeling of realistic nanoelectronic and quantum devices.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Bang Liu, Yang Zhong, Zhi-Xin Guo, Xin-Gao Gong, Hongjun Xiang. 2026-09-29. Linear-Scaling Quantum Transport from Machine-Learning Density Functional Theory Hamiltonians. https://arxiv.org/abs/2609.37058

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related papers

Crystal Dislocations as Atomic Scale Ratchets

The symmetry of a system's response to external stimuli is a fundamental concept in physics and materials science. At the microscopic scale, breaking this symmetry to achieve a rectified response is exceptionally difficult to engineer and remains rare in nature. Conventional micromechanics models of crystalline solids often assume a symmetric response to applied stress, where reversing the load simply inverts the direction of defect velocity without altering its magnitude. In this work, we report an atomic-scale, geometry-rooted mechanism that breaks this symmetry. Molecular dynamics simulations of face-centered cubic nickel reveal that dislocations containing atomic-scale jogs exhibit asymmetric mobility under opposite applied stresses: reversing the loading direction triggers significantly higher drag. This asymmetry arises from the coupling of two internal variables with different transformation parity: a non-affine displacement of an atom at the jog core, and a strain-like tensor associated with the advance of the dislocation. Because jogs are ubiquitous structures in plastic deformation, this discovery challenges classical descriptions of plastic deformation mechanisms, with direct implications for cyclic creep, and opens new pathways for defect engineering to enhance fatigue resistance.

cond-mat.mtrl-sci↗

The WEST code for large-scale excited-state materials simulations

We present WEST, an open-source plane-wave pseudopotential code for large-scale excited-state materials simulations, and describe its theoretical foundations, software architecture, and capabilities. WEST implements full-frequency GW, quantum defect embedding theory, the Bethe-Salpeter equation, and time-dependent density functional theory within a common algorithmic framework that avoids the explicit computation of virtual electronic states. By combining density functional and density matrix perturbation theory, low-rank representations of the dielectric screening and exact exchange, and localization techniques, WEST achieves favorable computational scaling with system size. The code supports the calculation of quasi-particle and neutral excitation energies, optical and photoluminescence spectra, excited-state forces, and non-adiabatic couplings, with interoperable workflows connecting to quantum chemistry, vibronic coupling, and quantum computing packages. A hierarchical parallelization strategy and GPU acceleration deliver near-ideal strong scaling to thousands of GPUs, enabling accurate excited-state simulations of systems with more than a thousand atoms. Representative applications, spanning the full optical cycle of solid-state spin defects, self-trapped excitons in metal-halide perovskites, and the optical response of liquid water and ice, demonstrate the accuracy and versatility of the code across diverse material classes. The capabilities implemented in WEST establish the code as a scalable platform for predictive excited-state simulations, high-throughput materials discovery, and the generation of high-fidelity datasets for machine learning in computational materials science.

cond-mat.mtrl-sci↗

Symmetry-Based Design Rules for Second-Harmonic Generation in Stacked and Twisted MoS2 Bilayers

Understanding how stacking controls the nonlinear optical response of two-dimensional materials is key to designing van der Waals heterostructures with tailored functionalities. Here, we establish a comprehensive symmetry-based framework mapping the structural configuration of MoS2 bilayers across four point groups (D3h, D3d, C3v, C3) to their second-order susceptibility tensor chi^(2). Using group-theory arguments benchmarked against first-principles response-function calculations, we demonstrate how symmetry breaking controls the activation and suppression of individual tensor elements in these systems. We show that the emergence of the in-plane component chi_xxx in twisted configurations (C3 group) induces a rigid azimuthal rotation of the second-harmonic generation polar lobes, which remains frequency-independent across the entire optical spectrum, locking to half of the structural twist angle. Our findings establish a direct, wavelength-independent optical route for twist-angle determination and provide a clear roadmap for engineering nonlinear optical responses in two-dimensional materials.

cond-mat.mtrl-sci↗