Searcharxiv⌕ Search

arXiv · 2610.11742

Can end-to-end learning from raw electronic structure explain magnetic anisotropy?

Abstract

Machine-learning models trained directly on electronic spectra can predict spin--orbit-driven properties, yet models with comparable predictive accuracy may learn different electronic dependencies. We examine this problem using magnetic anisotropy in atomic-scale magnets and a validation strategy designed to assess the physical relevance of learned spectral relationships. We compare a bidirectional gated recurrent unit and a one-dimensional convolutional neural network, both trained to predict magnetic anisotropy energy (MAE) from spin- and orbital-resolved scalar-relativistic densities of states (SR-DOS). Despite comparable in-domain (ID) accuracy, the architectures learn only partly overlapping spectral dependencies. Shapley additive explanations identify spectral features shared between the two architectures that can be associated with plausible spin--orbit-coupling pathways consistent with second-order perturbation theory (PT2). Adding PT2-derived MAE contributions to the model inputs has little effect on ID performance but can improve transfer beyond the training domain, with gains differing between architectures. Controlled spectral perturbations further demonstrate that similar attribution patterns do not imply the same functional dependence of the predicted MAE on spectral weight. The contrasting responses provide a functional context for architecture-dependent out-of-domain transfer. End-to-end learning can identify candidate electronic signatures of magnetic anisotropy. Their credible microscopic interpretation, however, rests on convergent evidence from predictive performance, model comparison, physical theory, controlled spectral interventions, and evaluation under distribution shift.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Rafał Topolnicki, Jan Navrátil, Piotr Błoński. 2026-10-08. Can end-to-end learning from raw electronic structure explain magnetic anisotropy?. https://arxiv.org/abs/2610.11742

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

KEEP EXPLORING

Related papers

Partially reactive force field for the UiO-66 metal-organic framework

UiO-66 is the most widely studied metal-organic framework, on account of its structural tunability given by its capacity of sustaining high amounts of point defects in its structure. Its synthesis mechanism is largely unknown, with only a few works mostly focused on the formation of the Zr-oxide cluster. In this work, a partially reactive force field to model UiO-66, nb-UiO-FF, is introduced. This force field incorporates node--ligand reactivity via a Morse potential and the introduction of dummy atoms to reproduce the anisotropic charge distribution of the Zr atoms in the node. nb-UiO-FF reproduces structural features of both UiO-66 and its isoreticular analog UiO-67 as well as framework stability with or without defects, activated or filled with N,N-dimethylformamide or ethanol. Defect generation and node--ligand binding energies are comparable with density functional theory values. The force field is further employed within a molecular dynamics scheme to study the early stages of solvothermal node--ligand binding. Species with structures corresponding to motifs present in UiO-66 are observed, along with other metastable species. This force field enables studying the self-assembly of UiO-66, as well as the formation of its point defects.

cond-mat.mtrl-sci↗

Electronic Properties of Ladder-Type Phenylenes Studied by Thermally-Assisted-Occupation Density Functional Theory

Accurate prediction of the electronic properties of extended $π$-conjugated systems with radical character remains a major theoretical challenge. To overcome this challenge, thermally-assisted-occupation density functional theory (TAO-DFT) has been developed in recent years. In this study, we employ TAO-DFT to systematically explore the electronic properties of ladder-type phenylenes ($n$-LPs), containing $n$ linearly fused four-membered carbon rings. Our calculations reveal that all investigated $n$-LPs (with $n$ = 1 ~ 40) possess singlet ground states. With increasing $n$-LP length, we observe a transition from the nonradical character of shorter $n$-LPs to the polyradical character of longer $n$-LPs. Notably, we identify a distinct damped periodic oscillation in the radical character of $n$-LPs, featuring highly correlated hotspots at specific lengths ($n = 3k - 1$, where $k$ are positive integers). The real-space representation of active orbitals confirms this global electronic behavior is governed by the intrinsic structural periodicity and completely delocalized nature of the active orbitals along the central ladder framework. These findings provide fundamental insights into the size-dependent electronic properties of $n$-LPs, guiding their rational design for future nanomaterial applications.

cond-mat.mtrl-sci↗

Knowledge-Guided Construction of Machine Learning Potentials for Reactive Behavior in Energetic Materials

Energetic materials involve multiple interactions, making reliable machine-learning potentials (MLPs) difficult to construct without extensive datasets. Here, we enhance the ability of the neural network interatomic potential (NNAP) to describe molecular systems using sphmulti, a refined spherical-harmonic basis set that combines extra radial basis with element-specific chemical weighting in each radial channel. We further integrate hyperactive learning, farthest-point sampling, and iterative sufficiency criteria with knowledge-guided key events, enabling the NNAP to retain essential information for describing the material system. For 3,3'-diamino-4,4'-azoxyfurazan, the resulting NNAP is trained on only 13,680 configurations yet captures key properties, including the isomerization barrier, pyrolysis activation energy, and shock Hugoniot behavior. NNAP-driven molecular dynamics simulations further reveal that pyrolysis proceeds through furazan-ring opening followed by chain reactions, whereas shock loading induces anisotropic hydrogen transfer driven by interlayer structural deformations. This work enables efficient and reliable MLPs for energetic materials.

cond-mat.mtrl-sci↗