Anmar Karmush

Pavlo Melnyk, Anmar Karmush, Mårten Wadenbäck et al.

Merging first-principles calculations with machine learning (ML), we aim to accelerate the exploration of catalytic behaviour in novel materials. We focus on two-dimensional (2D) Ti$_2$CT$_y$ MXenes, whose versatile surface chemistry makes them particularly compelling candidates for catalysis. Resolving their composition and structure under realistic conditions exceeds the reach of standard density functional theory (DFT) due to computational cost. To address this challenge, we generate a comprehensive dataset of 50,000 DFT calculations for training and 10,000 for testing, encompassing both Ti$_2$CT$_y$ MXene configurations and molecular systems, along with an additional test dataset with 1000 genuinely new, larger systems to investigate how well models generalise. We train and validate widely used and competitive machine learning interatomic potential (MLIP) models, including EquiformerV2, MACE, MatRIS, and UPET, that accurately predict atomic forces and formation energies -- quantities that DFT must repeatedly compute for structural and catalytic investigations -- for these 2D materials. This combined DFT-ML framework achieves computational acceleration on the order of approximately $1-4 \cdot 10^3$ (on a CPU) while maintaining desired-level accuracy (approximately +/- $10$ meV/A for forces and approximately +/- $1$ meV for per-atom energies), paving the way for more efficient investigations of MXene catalytic behaviour. Moreover, we perform an extensive qualitative evaluation of the trained models, showcasing the importance of comprehensive simulation-based comparison beyond benchmark metrics. The dataset and the trained models with the code are available at https://huggingface.co/datasets/CatalystAnonymous/catalyst_mxenes.

Ioannis Athanasiadis, Anmar Karmush, Michael Felsberg

In deep learning, functional similarity evaluation quantifies the extent to which independently trained models learn similar input--output relationships. In model stitching, functional similarity is framed as representation forward compatibility, i.e., whether the representations of two models can be aligned to solve a given task. Recent studies, however, highlight a critical limitation: models relying on different information cues can still produce compatible representations, making them appear misleadingly similar (Smith et al., 2025). We attribute this failure to standard model stitching being inherently blind to the invariance properties of the stitched models. To address this limitation, we introduce the forward--backward compatibility requirement under which we formulate the invariance-aware model stitching. Through analyzing key stitching configurations, we study the interplay between forward and backward compatibility, showing that invariance-aware model stitching provides a more principled approach to functional similarity evaluation while revealing functional discrepancies previously obscured.

Anmar Karmush, Cedric Mathieu Brandenburg, Soheil Ershadrad et al.

Tackling the task of materials generation, we aim to enhance the previously proposed All-atom Diffusion Transformer (ADiT) by introducing SymADiT, a symmetry-aware variant. To do so, we use a representation of materials based on Wyckoff positions. We follow ADiT and perform generative modelling in latent space, adapted to our symmetry-aware representation. By forcing the output of the generative model to adhere to the symmetry restrictions imposed by the generated crystal's space group and each atom's Wyckoff-position, the generated materials exhibit more realistic symmetry properties. We benchmark our method against both symmetry-aware and symmetry-agnostic models for materials generation and show competitive performance, generating stable, symmetric materials with a simple Transformer architecture.