arXiv subjects

Fabio Priante

Publications and source records attributed to Fabio Priante.

3 recordsLinked to original sources

arXiv2026

A Pathway to General-Purpose Scientific AI: Multimodal Comprehension of Scientific Images

Scientific figures and tables encode essential experimental evidence, yet remain difficult for digital libraries and multimodal AI systems to retrieve and interpret. The ALD/E-ImageMiner benchmark and ICDAR 2026 Competition on Information Extraction from Atomic Layer Deposition/Etching Scientific Figures provide 1,951 figures from 205 publications, expert-annotated for classification, data table extraction, summarization, and visual question answering. In these companion proceedings, we present a forward-looking perspective on how the benchmark can guide future scientific-image challenges. We examine how its tasks probe capabilities from visual and quantitative reading to domain-grounded reasoning and evidential justification, and how Bloom-informed question design can support deeper scientific understanding. We propose "scientific conceptual understanding from images" as a long-term benchmark objective, with future directions including broader domains and figure types, contextual and cross-document synthesis, hypothesis evaluation, provenance, uncertainty, counterfactual grounding, and open-ended multimodal research. This perspective connects the ICDAR 2026 challenge to a broader agenda for machine-actionable scientific visual knowledge and verifiable multimodal scientific AI.

cs.AI↗

arXiv2025

Improving atomic force microscopy structure discovery via style-translation

Atomic force microscopy (AFM) is a key tool for characterising nanoscale structures, with functionalised tips now offering detailed images of the atomic structure. In parallel, AFM simulations using the particle probe model provide a cost-effective approach for rapid AFM image generation. Using state-of-the-art machine learning models and substantial simulated datasets, properties such as molecular structure, electrostatic potential, and molecular graph can be predicted from AFM images. However, transferring model performance from simulated to experimental AFM images poses challenges due to the subtle variations in real experimental data compared to the seemingly flawless simulations. In this study, we explore style translation to augment simulated images and improve the predictive performance of machine learning models in surface property analysis. We reduce the style gap between simulated and experimental AFM images and demonstrate the method's effectiveness in enhancing structure discovery models through local structural property distribution comparisons. This research presents a novel approach to improving the efficiency of machine learning models in the absence of labelled experimental data.

cond-mat.mtrl-sci↗

arXiv2023

Accelerated lignocellulosic molecule adsorption structure determination

Here, we present a study combining Bayesian optimisation structural inference with the machine learning interatomic potential NequIP to accelerate and enable the study of the adsorption of the conformationally flexible lignocellulosic molecules $β$-D-xylose and 1,4-$β$-D-xylotetraose on a copper surface. The number of structure evaluations needed to map out the relevant potential energy surfaces are reduced by Bayesian optimisation, while NequIP minimises the time spent on each evaluation, ultimately resulting in cost-efficient and reliable sampling of large systems and configurational spaces. Although the applicability of Bayesian optimisation for the conformational analysis of the more flexible xylotetraose molecule is restricted by the sample complexity bottleneck, the latter can be effectively bypassed with external conformer search tools, such as the Conformer-Rotamer Ensemble Sampling Tool, facilitating the subsequent lower dimensional global minimum adsorption structure determination. Finally, we demonstrate the applicability of the described approach to find adsorption structures practically equivalent to the density functional theory counterparts at a fraction of the computational cost.

physics.chem-ph↗