analiza aiqbench
EP-Flow introduces a novel generative framework capable of predicting disordered crystal structures from chemical formulas alone, eliminating the need for unavailable site-level annotations. By utilizing an Occupancy Distribution Matrix within a flow matching architecture, the model effectively unifies ordered and disordered systems while satisfying strict physical constraints like mass conservation. This advancement represents a significant step forward in materials informatics, enabling the discovery of functional materials with intrinsic disorder that were previously difficult to model computationally.
EP-Flow: Disordered Crystal Structure Prediction without Site-Level Annotations
arXiv:2610.01315v1 Announce Type: new Abstract: Generative models have made rapid progress in ordered crystal structure prediction, yet many functional materials are intrinsically disordered, with substitutional mixing, vacancies, or interstitial species controlling their properties. Existing crystal generators either assume deterministic site occupations or require site-level disorder annotations, which are often unavailable when the chemical formula is the primary input. We formulate disordered crystal structure prediction through an Occupancy Distribution Matrix (ODM), a continuous site-by-species representation that unifies ordered crystals, solid solutions, vacancy disorder, and interstitial occupancy. A valid ODM must satisfy coupled site-wise occupancy, mass-conservation, and non-negativity constraints, placing each sample on a formula-dependent transportation polytope. We propose Entropic Polytope Flow (EP-Flow), a marginal-constrained flow matching framework that canonicalizes heterogeneous polytopes into a shared double-centered space, learns a marginal-preserving flow, and recovers feasible occupancies through a Sinkhorn inverse map. By jointly generating occupancies, fractional coordinates, and lattice parameters, EP-Flow achieves state-of-the-art performance on formula-conditioned disordered CSP benchmarks derived from COD and MPDS, substantially outperforming adapted ordered-crystal generators. Analyses further show that EP-Flow recovers sparse and chemically meaningful local disorder patterns rather than merely matching global composition statistics.
Abstract:Generative models have made rapid progress in ordered crystal structure prediction, yet many functional materials are intrinsically disordered, with substitutional mixing, vacancies, or interstitial species controlling their properties. Existing crystal generators either assume deterministic site occupations or require site-level disorder annotations, which are often unavailable when the chemical formula is the primary input. We formulate disordered crystal structure prediction through an Occupancy Distribution Matrix (ODM), a continuous site-by-species representation that unifies ordered crystals, solid solutions, vacancy disorder, and interstitial occupancy. A valid ODM must satisfy coupled site-wise occupancy, mass-conservation, and non-negativity constraints, placing each sample on a formula-dependent transportation polytope. We propose Entropic Polytope Flow (EP-Flow), a marginal-constrained flow matching framework that canonicalizes heterogeneous polytopes into a shared double-centered space, learns a marginal-preserving flow, and recovers feasible occupancies through a Sinkhorn inverse map. By jointly generating occupancies, fractional coordinates, and lattice parameters, EP-Flow achieves state-of-the-art performance on formula-conditioned disordered CSP benchmarks derived from COD and MPDS, substantially outperforming adapted ordered-crystal generators. Analyses further show that EP-Flow recovers sparse and chemically meaningful local disorder patterns rather than merely matching global composition statistics.
Machine Learning (cs.LG); Disordered Systems and Neural Networks (cond-mat.dis-nn)
arXiv:2610.01315 [cs.LG]
(or arXiv:2610.01315v1 [cs.LG] for this version)
https://doi.org/10.48550/arXiv.2610.01315 Focus to learn more arXiv-issued DOI via DataCite (pending registration)
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