Data-efficient machine learning for molecular crystal structure prediction. Issue 12 (18th February 2021)

• Record Type: Journal Article
• Authors: Wengert, Simon; Csányi, Gábor; Reuter, Karsten; Margraf, Johannes T.
• Is Part Of: Chemical science. Volume 12:Issue 12(2021)
• Page Start: 4536
• Page End: 4546
• Publication Date: 2021-02-18
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/d0sc05765g
• Languages: English
• ISSNs: 2041-6520

Abstract

Abstract : Using a cluster-based training scheme and a physical baseline, data efficient machine-learning models for crystal structure prediction are developed, enabling accurate structural relaxations of molecular crystals with unprecedented efficiency. Abstract : The combination of modern machine learning (ML) approaches with high-quality data from quantum mechanical (QM) calculations can yield models with an unrivalled accuracy/cost ratio. However, such methods are ultimately limited by the computational effort required to produce the reference data. In particular, reference calculations for periodic systems with many atoms can become prohibitively expensive for higher levels of theory. This trade-off is critical in the context of organic crystal structure prediction (CSP). Here, a data-efficient ML approach would be highly desirable, since screening a huge space of possible polymorphs in a narrow energy range requires the assessment of a large number of trial structures with high accuracy. In this contribution, we present tailored Δ-ML models that allow screening a wide range of crystal candidates while adequately describing the subtle interplay between intermolecular interactions such as H-bonding and many-body dispersion effects. This is achieved by enhancing a physics-based description of long-range interactions at the density functional tight binding (DFTB) level—for which an efficient implementation is available—with a short-range ML model trained on high-quality first-principles reference data. The presented workflow is broadly applicable to different molecular materials, without the need for a single periodic calculation at the reference level of theory. We show that this even allows the use of wavefunction methods in CSP.