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Konstantin S. Jakob

Publications and source records attributed to Konstantin S. Jakob.

2 recordsLinked to original sources

General-purpose LLMs as Constrained Crystal Composition Generators

The targeted discovery of inorganic materials remains challenging due to the vastness of compositional design spaces and the high cost of exhaustive screening. Task-specific generative artificial intelligence represents a particularly efficient alternative to screening, yet demands tedious collection of training data before providing real benefit. General-purpose large language models (LLMs) have recently shown tremendous potential for the targeted generation of single, optimal materials compositions without the need for task-specific fine-tuning. However, it is unclear whether LLMs generally pose an advantage compared to specialized generative models, in particular in large design spaces. Here, we demonstrate that such models are capable of covering entire regions of the targeted property space effectively and systematically. Using Elpasolite materials as an established benchmark for generative tasks in large chemical spaces, we find that an iterative prompt-and-response framework is able to recover on average 96% of all low-energy Elpasolites in the target region. This performance, driven mainly by iterative in-context learning, surpasses the generative abilities of previous, task-specific models. Our results establish general-purpose LLMs as flexible and accessible components for inverse materials design workflows.

cond-mat.mtrl-sci↗

A foundation model for atomistic materials chemistry

Atomistic simulations of matter, especially those that leverage first-principles (ab initio) electronic structure theory, provide a microscopic view of the world, underpinning much of our understanding of chemistry and materials science. Over the last decade or so, machine-learned force fields have transformed atomistic modeling by enabling simulations of ab initio quality over unprecedented time and length scales. However, early ML force fields have largely been limited by: (i) the substantial computational and human effort of developing and validating potentials for each particular system of interest; and (ii) a general lack of transferability from one chemical system to the next. Here we show that it is possible to create a general-purpose atomistic ML model, trained on a public dataset of moderate size, that is capable of running stable molecular dynamics for a wide range of molecules and materials. We demonstrate the power of the MACE-MP-0 model - and its qualitative and at times quantitative accuracy - on a diverse set of problems in the physical sciences, including properties of solids, liquids, gases, chemical reactions, interfaces and even the dynamics of a small protein. The model can be applied out of the box as a starting or "foundation" model for any atomistic system of interest and, when desired, can be fine-tuned on just a handful of application-specific data points to reach ab initio accuracy. Establishing that a stable force-field model can cover almost all materials changes atomistic modeling in a fundamental way: experienced users get reliable results much faster, and beginners face a lower barrier to entry. Foundation models thus represent a step towards democratising the revolution in atomic-scale modeling that has been brought about by ML force fields.

physics.chem-ph↗