Materials Property Prediction

Developing ceramic glazes is a costly, time-consuming process of trial and error due to complex chemistry, placing a significant burden on independent artists. While recent advances in multimodal AI offer a modern solution, the field lacks the large-scale datasets required to train these models. We propose GlazyBench, the first dataset for AI-assisted glaze design. Comprising 23,148 real glaze formulations, GlazyBench supports two primary tasks: predicting post-firing surface properties, such as color and transparency, from raw materials, and generating accurate visual representations of the glaze based on these properties. We establish comprehensive baselines for property prediction using traditional machine learning and large language models, alongside image generation benchmarks using deep generative and large multimodal models. Our experiments demonstrate promising yet challenging results. GlazyBench pioneers a new research direction in AI-assisted material design, providing a standardized benchmark for systematic evaluation.

Long-range electrostatics and polarization remain central obstacles to extending machine learning interatomic potentials (MLIPs) to ionic, polar, and interfacial systems. Here we introduce a semi-local framework for learning electrostatics from energies and forces using polarizable atomic multipoles. Local equivariant descriptors predict environment-dependent latent monopoles, dipoles, and quadrupoles, while residual non-local charge transfer and polarization are captured by non-self-consistent linear response in induced charges and dipoles. Across four diverse benchmarks and four short-range MLIP architectures, the multipole hierarchy and response terms systematically improve potential energy surface accuracy, with the largest gains in systems where long-range effects are essential. More importantly, physically meaningful electrical responses emerge without direct supervision. The learned latent multipoles yield accurate Born effective charge tensors and infrared spectra in close agreement with experiments. The induced-dipole extension introduces new capabilities: it predicts polarizabilities and thereby enables semi-quantitative Raman spectra for bulk water and hybrid MAPbI$_3$ perovskite, as well as the essential features of the surface-specific vibrational sum-frequency generation spectrum at the water-air interface. In ferroelectric HfO$_2$, the predicted electrical response also captures LO-TO splitting and polarization switching. This systematically improvable, physically transparent framework enables MLIPs trained on standard energy and force labels to predict polarization-sensitive observables.

Materials science data collection can be expensive, making dataset reuse and long-term utility important for future discovery. In practice, data collection often prioritizes properties of current interest while other properties are excluded from the acquisition process. This can produce datasets that are well suited for current objectives but lose information needed for properties of future interest. Here, we present how to construct datasets that remain informative for both. We develop and evaluate acquisition frameworks that combine predictive disagreement with diversity in material features, predicted outcomes, or both. We test these approaches across four DFT datasets and an experimental thermoelectric dataset. Diversity inclusion in dataset construction can reduce present and future objectives trade-off by preserving a broader range of materials and property behavior during acquisition. Across all datasets, the Non-dominated Sorting Genetic Algorithm II with disagreements and feature diversity (NSGA-II Dis. + diversity) framework developed in this work provides the most robust balance between current and future objectives. It maintains prediction performance above random sampling for current objectives while mitigating bias on excluded properties and, in many cases, improving their performance beyond random sampling. This diversity-aware acquisition framework provides a practical route to building materials datasets with unbiased quality entries and mitigating cold-start limitations in subsequent modeling and discovery campaigns.

Shallow nanoindentation, needed for thin layers, individual phases and small volumes, gives hardness inflated by the indentation size effect (ISE). The Nix-Gao correction reduces this inflation but requires deep indentations of the same material, often impossible in such samples. We present a data-efficient workflow, trained on a few reference materials, that predicts a high-load reference hardness from a single shallow indentation. Seven models were trained on 703 indentations (5-350 mN) on three steels (2.0-6.5 GPa): Ridge regression, Random Forest, XGBoost, two feed-forward networks, and two physics-constrained neural networks (PCNNs) that apply a bounded learned correction q as H_app/sqrt(1+q). Over five seeds, models were tested on an external steel not used for training and indented at different loads, in leave-one-steel-out folds, and on fused silica, an out-of-domain material where all models failed. Random Forest and XGBoost, the best on the development set, transferred worst over all loads (MAPE 10.2 and 8.5%), whereas Ridge regression, the PCNNs and one feed-forward network reached 3.7-4.8%; with three training steels, development-set accuracy thus did not indicate accuracy on an unseen steel. From only the external steel's 3-15 mN indentations, the smooth (non-tree) models estimated the reference within 0.03-0.19 GPa on average. The PCNNs matched the linear baseline within the training hardness range and were the most accurate for a held-out steel softer than the training steels, but failed for a harder one. The workflow uses no steel-specific inputs and can be retrained for other material classes.

Accurate bandgap prediction is crucial for semiconductor applications, yet machine learning models trained on computational data often struggle to generalize to experimental bandgap measurements. Challenges related to data fidelity, domain generalization, and model interpretability remain insufficiently addressed in existing evaluation frameworks. To bridge this gap, we introduce RealMat-BaG, a benchmark for assessing model reliability under experimentally relevant conditions. We curate an open-access dataset of experimental bandgaps with aligned crystal structures and compare graph neural networks as well as classical machine learning baselines. Our framework evaluates performance across statistical and domain-based splits, examines transfer from DFT-computed to experimental bandgaps, and analyzes interpretability at both elemental-property and structural levels. Our results reveal the fundamental generalization limitations of current bandgap prediction models and establish a benchmark aligned with experimental measurements for developing more reliable learning strategies for materials discovery.

Accurately estimating friction coefficients between arbitrary material pairs is critical for robotics, digital fabrication, and physics-based simulation, but exhaustive pairwise testing scales quadratically with the number of materials. We introduce a proxy-based modeling framework that approximates any pairwise friction $f(A,B)$ from a small, fixed set of proxy materials $C=[c_1,\dots,c_k]$ by learning a per-material embedding $z_A = g(f(A,c1),\dots,f(A,ck))$ and a fusion function $p$ such that $f(A,B)\approx p\big(z_A,z_B\big)$. We present deterministic and probabilistic realizations of $g$ and $p$, procedures for selecting diverse proxy sets, and mechanisms for handling missing or noisy proxy measurements. The learned embeddings are compact, interpretable, and enable calibrated uncertainty estimates for downstream decision making. On simulated and measured friction datasets, our approach achieves high predictive accuracy, robust performance with partial observations, and substantial experimental savings by significantly reducing pairwise testing.

Artificial intelligence has accelerated materials discovery through high-throughput prediction and generation, yet the decision problem remains a formidable bottleneck. While current AI systems readily propose millions of candidates, navigating the decision regarding a viable experimental target requires resolving multi-dimensional judgments across atomic-scale numerical computation and high-level semantic reasoning. Here we present ElementsClaw, an agentic framework for materials discovery that orchestrates a suite of Large Atomic Model (LAM) tools finetuned from our proposed 1-billion-parameter model Elements for numerical computation, while leveraging Large Language Models (LLMs) for semantic reasoning. Applied to superconductors, ElementsClaw rediscovers 66 experimentally verified superconductors that are absent from the standard SuperCon3D database. Scaling to 2.4 million equilibrium crystals, ElementsClaw identifies 68,000 high-confidence candidates in just 28 GPU hours (https://developer.damo-academy.com/material), expanding known superconducting space by orders of magnitude compared to datasets curated over decades. Guided by the agent's reasoning, we experimentally synthesize and verify four novel superconductors: the motif-guided Zr$_3$ScRe$_8$ ($T_c$ = 6.5 K), the de novo generated HfZrRe$_4$ ($T_c$ = 5.9 K), the structurally reinterpreted Zr$_4$VRe$_7$ ($T_c$ = 3.5 K), and the database-latent Hf$_{21}$Re$_{25}$ ($T_c$ = 2.5 K). Together, our results establish a knowledge integrated, autonomously orchestrated, and experimentally grounded paradigm for materials discovery.

High-entropy alloys (HEAs) have attracted growing attention for their exceptional mechanical and thermal properties arising from complex atomic configurations. In this paper, we propose crystal fractional graph neural network for predicting the energy of high-entropy alloys by explicitly integrating both local atomic environments and global compositional information. The model consists of three components: a crystal graph neural network, which employs graph attention network layers to learn local interactions among 16 on-site atoms within the crystal lattice; fractional neural network, a fully connected network that embeds the global fraction of constituent elements; and feature fusion neural network, which fuses the outputs of the two submodels to predict the total crystal energy. We train the model on a dataset of 1,049 crystal structures and validate it on 198 quaternary structures, optimizing all hyperparameters via Optuna. Our results show that our model achieves an RMSE comparable to first-principles calculations and maintains high accuracy even for low-energy configurations. However, the model exhibits limitations in handling large crystal cells, which we aim to address in future work to extend its applicability to more complex systems.

Metal-organic frameworks (MOFs) are a major target of machine-learning-based property prediction, yet most models assume that a single framework representation maps to a single property value. This assumption becomes problematic for experimental MOFs, where samples reported as the same framework can exhibit different properties because of differences in crystallinity, phase purity, defects, and other sample-dependent factors. Here we introduce Experimental X-ray Diffraction Integrated Transformer (EXIT), a multimodal transformer for sample-aware prediction of MOF properties that combines MOFid with X-ray diffraction (XRD). In EXIT, MOFid encodes MOF identity, whereas XRD provides complementary information about the experimentally realized sample state. EXIT is pre-trained on one million hypothetical MOFs with simulated XRD to learn transferable representations, leading to improved downstream performance relative to existing approaches. EXIT is fine-tuned on literature-derived experimental datasets for surface area and pore volume prediction. Incorporating experimental XRD improves predictive performance relative to models without experimental XRD, and attention analysis and sample-level case studies further show that EXIT assigns different predictions to samples sharing the same MOF identity when their XRD patterns differ. These results establish a practical step from framework-aware to sample-aware MOF property prediction and highlight the value of incorporating experimental characterization into porous materials informatics.

Accurate methane sorption prediction across heterogeneous coal ranks requires models that combine thermodynamic consistency, efficient knowledge transfer across data-scarce geological systems, and calibrated uncertainty estimates, capabilities that are rarely addressed together in existing frameworks. We present a physics-informed transfer learning framework that adapts a hydrogen sorption PINN to methane sorption prediction via Elastic Weight Consolidation, coal-specific feature engineering, and a three-phase curriculum that progressively balances transfer preservation with thermodynamic fine-tuning. Trained on 993 equilibrium measurements from 114 independent coal experiments spanning lignite to anthracite, the framework achieves R2 = 0.932 on held-out coal samples, a 227% improvement over pressure-only classical isotherms, while hydrogen pre-training delivers 18.9% lower RMSE and 19.4% faster convergence than random initialization. Five Bayesian uncertainty quantification approaches reveal a systematic divergence in performance across physics-constrained architectures. Monte Carlo Dropout achieves well-calibrated uncertainty at minimal overhead, while deep ensembles, regardless of architectural diversity or initialization strategy, exhibit performance degradation because shared physics constraints narrow the admissible solution manifold. SHAP and ALE analyses confirm that learned representations remain physically interpretable and aligned with established coal sorption mechanisms: moisture-volatile interactions are most influential, pressure-temperature coupling captures thermodynamic co-dependence, and features exhibit non-monotonic effects. These results identify Monte Carlo Dropout as the best-performing UQ method in this physics-constrained transfer learning framework, and demonstrate cross-gas transfer learning as a data-efficient strategy for geological material modeling.

We present XANE(3), a physics-based E(3)-equivariant graph neural network for predicting X-ray absorption near-edge structure (XANES) spectra directly from atomic structures. The model combines tensor-product message passing with spherical harmonic edge features, absorber-query attention pooling, custom equivariant layer normalization, adaptive gated residual connections, and a spectral readout based on a multi-scale Gaussian basis with an optional sigmoidal background term. To improve line-shape fidelity, training is performed with a composite objective that includes pointwise spectral reconstruction together with first- and second-derivative matching terms. We evaluate the model on a dataset of 5,941 FDMNES simulations of iron oxide surface facets and obtain a spectrum mean squared error of $1.0 \times 10^{-3}$ on the test set. The model accurately reproduces the main edge structure, relative peak intensities, pre-edge features, and post-edge oscillations. Ablation studies show that the derivative-aware objective, custom equivariant normalization, absorber-conditioned attention pooling, adaptive gated residual mixing, and global background term each improve performance. Interestingly, a capacity-matched scalar-only variant achieves comparable pointwise reconstruction error but reduced derivative-level fidelity, indicating that explicit tensorial channels are not strictly required for low intensity error on this dataset, although they remain beneficial for capturing finer spectral structure. These results establish XANE(3) as an accurate and efficient surrogate for XANES simulation and offer a promising route toward accelerated spectral prediction, ML-assisted spectroscopy, and data-driven materials discovery.

Accurate material recognition is a fundamental capability for intelligent perception systems to interact safely and effectively with the physical world. For instance, distinguishing visually similar objects like glass and plastic cups is critical for safety but challenging for vision-based methods due to specular reflections, transparency, and visual deception. While millimeter-wave (mmWave) radar offers robust material sensing regardless of lighting, existing camera-radar fusion methods are limited to closed-set categories and lack semantic interpretability. In this paper, we introduce VLMaterial, a training-free framework that fuses vision-language models (VLMs) with domain-specific radar knowledge for physics-grounded material identification. First, we propose a dual-pipeline architecture: an optical pipeline uses the segment anything model and VLM for material candidate proposals, while an electromagnetic characterization pipeline extracts the intrinsic dielectric constant from radar signals via an effective peak reflection cell area (PRCA) method and weighted vector synthesis. Second, we employ a context-augmented generation (CAG) strategy to equip the VLM with radar-specific physical knowledge, enabling it to interpret electromagnetic parameters as stable references. Third, an adaptive fusion mechanism is introduced to intelligently integrate outputs from both sensors by resolving cross-modal conflicts based on uncertainty estimation. We evaluated VLMaterial in over 120 real-world experiments involving 41 diverse everyday objects and 4 typical visually deceptive counterfeits across varying environments. Experimental results demonstrate that VLMaterial achieves a recognition accuracy of 96.08%, delivering performance on par with state-of-the-art closed-set benchmarks while eliminating the need for extensive task-specific data collection and training.

Current large language models require hundreds of billions of parameters yet struggle with domain-specific reasoning and tool coordination in materials science. Here, we present MatBrain, a lightweight collaborative agent system with two synergistic models specialization for crystal materials research. MatBrain employs a dual-model architecture: Mat-R1 (30B parameters) as the analytical model providing expert-level domain reasoning, and Mat-T1 (14B parameters) as the executive model orchestrating tool-based actions. Entropy analysis confirms that this architecture resolves the conflict between tool planning and analytical reasoning by decoupling their distinct entropy dynamics. Enabled by this dual-model architecture and structural efficiency, MatBrain significantly outperforms larger general-purpose models while reducing the hardware deployment barrier by over 95%. MatBrain exhibits versatility across structure generation, property prediction, and synthesis planning tasks. Applied to catalyst design, MatBrain generated 30,000 candidate structures and identified 38 promising materials within 48 hours, achieving approximately 100-fold acceleration over traditional approaches. These results demonstrate the potential of lightweight collaborative intelligence for advancing materials research capabilities.

Systematic chemical names, such as IUPAC-style nomenclature for metal-organic frameworks (MOFs), contain rich structural and compositional information in a standardized textual format. Here we introduce ReadMOF, which is, to our knowledge, the first nomenclature-free machine learning framework that leverages these names to model structure-property relationships without requiring atomic coordinates or connectivity graphs. By employing pretrained language models, ReadMOF converts systematic MOF names from the Cambridge Structural Database (CSD) into vector embeddings that closely represent traditional structure-based descriptors. These embeddings enable applications in materials informatics, including property prediction, similarity retrieval, and clustering, with performance comparable to geometry-dependent methods. When combined with large language models, ReadMOF also establishes chemically meaningful reasoning ability with textual input only. Our results show that structured chemical language, interpreted through modern natural language processing techniques, can provide a scalable, interpretable, and geometry-independent alternative to conventional molecular representations. This approach opens new opportunities for language-driven discovery in materials science.

Magnetic point-group analysis classifies altermagnets but returns only a binary symmetry verdict, leaving spin-splitting energy (SSE) inaccessible without spin-polarized density functional theory (DFT). This binary ceiling is not fundamental. Sublattice symmetry breaking is promoted here to a continuous, DFT-free scalar -- the Motif Symmetry-Breaking Index (MSBI) -- that quantifies $\mathcal{PT}$-symmetry breaking between antiparallel magnetic motifs directly from crystal coordinates. SHAP analysis of an XGBoost surrogate trained on 3,851 DFT-labeled binary structures identifies three dominant descriptors: MSBI (symmetry-breaking axis), motif packing fraction MPF (superexchange axis), and the $p/d$ electron ratio (covalency axis), each mapping onto a directly tunable experimental handle. A controlled VO--CrSb comparison within the same P$6_3$/mmc host lattice demonstrates that composition alone boosts SSE sevenfold. Bayesian optimization over this three-axis space, followed by independent DFT validation, recovers $α$-NiS (SSE $= 0.823$,eV) as cross-validation against an independent symmetry-based prediction and identifies three previously unrecognized high-SSE candidates -- square-planar FeS (1.297,eV), octahedral CoS (1.103,eV), and FeAs (1.089,eV) -- all matching or exceeding CrSb. Square-planar Fe--S is proposed as a transferable coordination motif for giant altermagnetic spin splitting, advancing altermagnet design from symmetry classification to continuous quantitative optimization.

The past few years have witnessed vibrant efforts in discovering new two-dimensional (2D) semiconductor materials from both academia and the industry, due to their promising potential in resolving the severe performance deterioration of traditional semiconductors resulting from condensed silicon thickness. However, existing methods (e.g., Density Functional Theory (DFT) or machine-learning-based approaches) suffer from various challenges such as small datasets, and reliability and trustworthiness issues. To bridge this gap, we propose SemiConLens, a visual analytics approach to combine human expertise with the power of ML to enable effective and reliable 2D semiconductor discovery. Specifically, we first develop a new Correlation Aware Multivariate Imputation (CAMI) method and use ML models like autoencoder, which can better learn from limited data and reveal uncertainty, to address the challenge of sparse data in semiconductivity prediction. Built upon this, our visualization module, consisting of three visualization views with linked interactions, allows material researchers to interactively filter, discover and compare 2D semiconductor candidates. A novel circular glyph design and a new cluster-aware layout optimization approach are proposed to effectively display all the user-configurable key attributes and possible prediction uncertainties of each semiconductor candidate, ensuring a reliable and trustable 2D semiconductor discovery. We assess SemiConLens through quantitative evaluations, expert interviews, and use cases. The results demonstrate SemiConLens's capability to help material researchers conduct effective discovery of desirable 2D semiconductors.

The discovery of new energetic materials is critical for advancing technologies from defense to private industry. However, experimental approaches remain slow and expensive while computational alternatives require accurate material property inputs that are often costly to obtain, limiting their ability to efficiently predict detonation performance across a vast chemical space. We address this challenge through an active learning strategy that integrates density functional theory calculations, thermochemical modeling, message-passing neural networks, and Bayesian optimization. The resulting high-throughput workflow iteratively expands the training dataset by selecting new molecules in a targeted manner that balances the exploration of broad chemical space with the exploitation of promising high-performing candidates. This approach yields the largest publicly available database of potential CHNO explosives drawn from an initial pool of more than 70 billion candidates and a generalizable surrogate model capable of accurately predicting detonation performance (R$^2$ > 0.98). Feature importance analysis on this largest-to-date dataset reveals that oxygen balance is the dominant driver of detonation performance, complemented by contributions from local electronic structure, density, and the presence of specific functional groups. Cheminformatics analysis highlights how energetic materials with similar performance metrics tend to cluster in distinct chemical spaces offering a clearer direction for future synthesis studies. Together, the surrogate model, database, and resulting chemical insights provide a valuable foundation for high-throughput screening and targeted discovery of new energetic materials spanning diverse and previously unexplored regions of chemical space.

Characterizing crystalline energy landscapes is essential to predicting thermodynamic stability, electronic structure, and functional behavior. While machine learning (ML) enables rapid property predictions, the "black-box" nature of most models limits their utility for generating new scientific insights. Here, we introduce Kolmogorov-Arnold Networks (KANs) as an interpretable framework to bridge this gap. Unlike conventional neural networks with fixed activation functions, KANs employ learnable functions that reveal underlying physical relationships. We developed the Element-Weighted KAN, a composition-only model that achieves state-of-the-art accuracy in predicting formation energy, band gap, and work function across large-scale datasets. Crucially, without any explicit physical constraints, KANs uncover interpretable chemical trends aligned with the periodic table and quantum mechanical principles through embedding analysis, correlation studies, and principal component analysis. These results demonstrate that KANs provide a powerful framework with high predictive performance and scientific interpretability, establishing a new paradigm for transparent, chemistry-based materials informatics.

All-atom molecular dynamics (MD) simulations can predict polymer properties from molecular structure, yet their execution requires specialized expertise in force field selection, system construction, equilibration, and property extraction. We present PolyJarvis, a platform in which a planning agent produces a validated run plan that deterministic stage scripts execute through established simulation toolkits, Enhanced Monte Carlo (EMC) for system construction and LAMMPS for molecular dynamics, exposed as Model Context Protocol (MCP) servers, with a recovery agent consulted only on structured failures and within a fixed decision budget. Given a repeat-unit SMILES string and target properties, PolyJarvis constructs the amorphous cell, equilibrates it under a mechanized convergence gate, and computes target properties. Validation is conducted on seven amorphous homopolymers, each run as three replicates that share a protocol frozen per system and use independent random seeds, namely polyethylene (PE), atactic polystyrene (aPS), syndiotactic poly(vinyl chloride) (sPVC), poly(L-lactic acid) (PLLA), poly(ethylene glycol) (PEG), poly(ether ether ketone) (PEEK), and polysulfone (PSU). Against experimental references, 13 of 19 graded comparisons meet the acceptance criteria (density 5 of 7, glass transition 4 of 7, bulk modulus 4 of 5). The failures are concentrated in the PCFF systems: under-density of aPS and PEG, overestimated glass transitions of the stiff PLLA and PEEK backbones, and an overstiff PEG bulk modulus.

Accurate prediction of hydrogen sorption in fine-grained geological materials is essential for evaluating underground hydrogen storage capacity, assessing caprock integrity, and characterizing hydrogen migration in subsurface energy systems. Classical isotherm models perform well at the individual-sample level but fail when generalized across heterogeneous populations, with the coefficient of determination collapsing from 0.80-0.90 for single-sample fits to 0.09-0.38 for aggregated multi-sample datasets. We present a multi-scale physics-informed neural network framework that addresses this limitation by embedding classical adsorption theory and thermodynamic constraints directly into the learning process. The framework utilizes 1,987 hydrogen sorption isotherm measurements across clays, shales, coals, supplemented by 224 characteristic uptake measurements. A seven-category physics-informed feature engineering scheme generates 62 thermodynamically meaningful descriptors from raw material characterization data. The loss function enforces saturation limits, a monotonic pressure response, and Van't Hoff temperature dependence via penalty weighting, while a three-phase curriculum-based training strategy ensures stable integration of competing physical constraints. An architecture-diverse ensemble of ten members provides calibrated uncertainty quantification, with post-hoc temperature scaling achieving target prediction interval coverage. The optimized PINN achieves R2 = 0.9544, RMSE = 0.0484 mmol/g, and MAE = 0.0231 mmol/g on the held-out test set, with 98.6% monotonicity satisfaction and zero non-physical negative predictions. Physics-informed regularization yields a 10-15% cross-lithology generalization advantage over a well-tuned random forest under leave-one-lithology-out validation, confirming that thermodynamic constraints transfer meaningfully across geological boundaries.

Machine learning offers powerful tools to support experimental techniques, particularly for extracting latent features from large datasets. In magnetic materials, accurately estimating the interfacial Dzyaloshinskii-Moriya interaction strength remains challenging, as existing experimental methods often rely on indirect measurements and can yield inconsistent results across techniques. Because this interaction is often extracted experimentally from bubble domain expansion, we investigate whether bubble textures alone contain sufficient and reliable information for data driven DMI inference. We therefore develop a compact convolutional neural network trained on a comprehensive micromagnetic dataset of magnetic bubble domains designed to emulate magneto optical Kerr effect imaging, including structural non uniformity, additive noise, and image pixelation. The proposed network demonstrates strong robustness against sample inhomogeneities, noise, and reduced spatial resolution. Furthermore, it exhibits reliable generalization by accurately predicting DMI values outside the trained interval. These results support the use of machine learning as a fast and quantitative tool to characterize magnetic textures with interfacial DMI.

Estimating the material property field of 3D assets is critical for physics-based simulation, robotics, and digital twin generation. Existing vision-based approaches are either too expensive and slow or rely on 3D information. We present SLAT-Phys, an end-to-end method that predicts spatially varying material property fields of 3D assets directly from a single RGB image without explicit 3D reconstruction. Our approach leverages spatially organised latent features from a pretrained 3D asset generation model that encodes rich geometry and semantic prior, and trains a lightweight neural decoder to estimate Young's modulus, density, and Poisson's ratio. The coarse volumetric layout and semantic cues of the latent representation about object geometry and appearance enable accurate material estimation. Our experiments demonstrate that our method provides competitive accuracy in predicting continuous material parameters when compared against prior approaches, while significantly reducing computation time. In particular, SLAT-Phys requires only 9.9 seconds per object on an NVIDIA RTXA5000 GPU and avoids reconstruction and voxelization preprocessing. This results in 120x speedup compared to prior methods and enables faster material property estimation from a single image.

Accurate prediction of mechanical properties of steel during hot rolling processes, such as Thin Slab Direct Rolling (TSDR), remains challenging due to complex interactions among chemical compositions, processing parameters, and resultant microstructures. Traditional empirical and experimental methodologies, while effective, are often resource-intensive and lack adaptability to varied production conditions. Moreover, most existing approaches do not explicitly leverage the strong correlations among key mechanical properties, missing an opportunity to improve predictive accuracy through multitask learning. To address this, we present a multitask learning framework that injects multitask awareness into the prior of TabPFN--a transformer-based foundation model for in-context learning on tabular data--through novel fine-tuning strategies. Originally designed for single-target regression or classification, we augment TabPFN's prior with two complementary approaches: (i) target averaging, which provides a unified scalar signal compatible with TabPFN's single-target architecture, and (ii) task-specific adapters, which introduce task-specific supervision during fine-tuning. These strategies jointly guide the model toward a multitask-informed prior that captures cross-property relationships among key mechanical metrics. Extensive experiments on an industrial TSDR dataset demonstrate that our multitask adaptations outperform classical machine learning methods and recent state-of-the-art tabular learning models across multiple evaluation metrics. Notably, our approach enhances both predictive accuracy and computational efficiency compared to task-specific fine-tuning, demonstrating that multitask-aware prior adaptation enables foundation models for tabular data to deliver scalable, rapid, and reliable deployment for automated industrial quality control and process optimization in TSDR.

Modern concrete must simultaneously satisfy evolving demands for mechanical performance, workability, durability, and sustainability, making mix designs increasingly complex. Recent studies leveraging Artificial Intelligence (AI) and Machine Learning (ML) models show promise for predicting compressive strength and guiding mix optimization, but most existing efforts are based on proprietary industrial datasets and closed-source implementations. Here we introduce BOxCrete, an open-source probabilistic modeling and optimization framework trained on a new open-access dataset of over 500 strength measurements (1-15 ksi) from 123 mixtures - 69 mortar and 54 concrete mixes tested at five curing ages (1, 3, 5, 14, and 28 days). BOxCrete leverages Gaussian Process (GP) regression to predict strength development, achieving average R$^2$ = 0.94 and RMSE = 0.69 ksi, quantify uncertainty, and carry out multi-objective optimization of compressive strength and embodied carbon. The dataset and model establish a reproducible open-source foundation for data-driven development of AI-based optimized mix designs.

Geotechnical site characterisation relies on sparse, heterogeneous borehole data, where uncertainty quantification and interpretability matter as much as predictive accuracy. We evaluate TabPFN~\citep{Hollmann2025}, a tabular foundation model, and its tabpfn-extensions library on two geotechnical tasks: (1) soil-type classification from N-value and shear-wave velocity data as a controlled illustrative case, and (2) iterative imputation of five mechanical parameters ($s_\mathrm{u}$, $E_{\mathrm{u}}$, ${σ'}_\mathrm{p}$, $C_\mathrm{c}$, $C_\mathrm{v}$) in BM/AirportSoilProperties/2/2025. Without retraining, we apply cosine-similarity analysis to TabPFN embeddings, visualise predictive distributions, and compute SHAP attributions. On the regression benchmark we compare TabPFN with mean imputation, linear regression, random forests, XGBoost, and HBM; introduce a proxy decomposition of predictive uncertainty across context-perturbation classes; and propagate marginal $C_\mathrm{c}$ and ${σ'}_\mathrm{p}$ distributions through a one-dimensional consolidation model to obtain the reliability index $β$ and serviceability exceedance probability $P_\mathrm{f}$. Embeddings exhibit label-consistent Clay/Sand grouping; iterative imputation reduces RMSE for all five targets, with TabPFN lowest on four; SHAP attributions are consistent with the Skempton compression-index correlation and the inverse preconsolidation-pressure-water-content dependence; the within-posterior component is largest in the proxy decomposition. We position the contribution as a worked evaluation workflow that may complement established methods for data-scarce geotechnics, not as algorithmic innovation.

Accurate prediction of permeability tensors from pore-scale microstructure images is essential for subsurface flow modeling, yet direct numerical simulation requires hours per sample, fundamentally limiting large-scale uncertainty quantification and reservoir optimization workflows. A physics-informed deep learning framework is presented that resolves this bottleneck by combining a MaxViT hybrid CNN-Transformer architecture with progressive transfer learning and differentiable physical constraints. MaxViT's multi-axis attention mechanism simultaneously resolves grain-scale pore-throat geometry via block-local operations and REV-scale connectivity statistics through grid-global operations, providing the spatial hierarchy that permeability tensor prediction physically requires. Training on 20000 synthetic porous media samples spanning three orders of magnitude in permeability, a three-phase progressive curriculum advances from an ImageNet-pretrained baseline with D4-equivariant augmentation and tensor transformation, through component-weighted loss prioritizing off-diagonal coupling, to frozen-backbone transfer learning with porosity conditioning via Feature-wise Linear Modulation (FiLM). Onsager reciprocity and positive definiteness are enforced via differentiable penalty terms. On a held-out test set of 4000 samples, the framework achieves variance-weighted R2 = 0.9960 (R2_Kxx = 0.9967, R2_Kxy = 0.9758), a 33% reduction in unexplained variance over the supervised baseline. The results offer three transferable principles for physics-informed scientific machine learning: large-scale visual pretraining transfers effectively across domain boundaries; physical constraints are most robustly integrated as differentiable architectural components; and progressive training guided by diagnostic failure-mode analysis enables unambiguous attribution of performance gains across methodological stages.

The success of large-scale pretraining in NLP and computer vision has catalyzed growing efforts to develop analogous foundation models for the physical sciences. However, pretraining strategies using atomistic data remain underexplored. To date, large-scale supervised pretraining on DFT force-energy labels has provided the strongest performance gains to downstream property prediction, out-performing existing methods of self-supervised learning (SSL) which remain limited to ground-state geometries, and/or single domains of atomistic data. We address these shortcomings with Self-Conditioned Denoising (SCD), a backbone-agnostic reconstruction objective that utilizes self-embeddings for conditional denoising across any domain of atomistic data, including small molecules, proteins, periodic materials, and 'non-equilibrium' geometries. When controlled for backbone architecture and pretraining dataset, SCD significantly outperforms previous SSL methods on downstream benchmarks and matches or exceeds the performance of supervised force-energy pretraining. We show that a small, fast GNN pretrained by SCD can achieve competitive or superior performance to larger models pretrained on significantly larger labeled or unlabeled datasets, across tasks in multiple domains. Our code is available at: https://github.com/TyJPerez/SelfConditionedDenoisingAtoms

Four-dimensional scanning transmission electron microscopy (4D-STEM) provides rich, atomic-scale insights into materials structures. However, extracting specific physical properties - such as polarization directions essential for understanding functional properties of ferroelectrics - remains a significant challenge. In this study, we systematically benchmark multiple machine learning models, namely ResNet, VGG, a custom convolutional neural network, and PCA-informed k-Nearest Neighbors, to automate the detection of polarization directions from 4D-STEM diffraction patterns in ferroelectric potassium sodium niobate. While models trained on synthetic data achieve high accuracy on idealized synthetic diffraction patterns of equivalent thickness, the domain gap between simulation and experiment remains a critical barrier to real-world deployment. In this context, a custom made prototype representation training regime and PCA-based methods, combined with data augmentation and filtering, can better bridge this gap. Error analysis reveals periodic missclassification patterns, indicating that not all diffraction patterns carry enough information for a successful classification. Additionally, our qualitative analysis demonstrates that irregularities in the model's prediction patterns correlate with defects in the crystal structure, suggesting that supervised models could be used for detecting structural defects. These findings guide the development of robust, transferable machine learning tools for electron microscopy analysis.

Predicting the stress-strain behaviors of additively manufactured materials is crucial for part qualification in additive manufacturing (AM). Conventional physics-based constitutive models often oversimplify material properties, while data-driven machine learning (ML) models often lack physical consistency and interpretability. To address these issues, we propose a physics-informed machine learning (PIML) framework to improve the predictive performance and physical consistency for predicting the stress-strain curves of additively manufactured polymers and metals. A polynomial regression model is used to predict the yield point from AM process parameters, then stress-strain curves are segmented into elastic and plastic regions. Two long short-term memory (LSTM) models are trained to predict two regions separately. For the elastic region, Hooke's law is embedded into the LSTM model for both polymer and metal. For the plastic region, Voce hardening law and Hollomon's law are embedded into the LSTM model for polymer and metal, respectively. The loss-based and activation-based PIML architectures are developed by embedding the physical laws into the loss and activation functions, respectively. The performance of the two PIML architectures are compared with two LSTM-based ML models, three additional ML models, and a physics-based constitutive model. These models are built on experimental data collected from two additively manufactured polymers (i.e., Nylon and carbon fiber-acrylonitrile butadiene styrene) and two additively manufactured metals (i.e., AlSi10Mg and Ti6Al4V). Experimental results demonstrate that two PIML architectures consistently outperform the other models. The segmental predictive model with activation-based PIML architecture achieves the lowest MAPE of 10.46+/-0.81% and the highest R^2 of 0.82+/-0.05 arocss four datasets.

Predicting the mechanical properties of polysulfone (PSF) membranes from structural descriptors remains challenging due to extreme data scarcity typical of experimental studies. To investigate this issue, this study benchmarked knowledge-driven inference using four large language models (LLMs) (DeepSeek-V3, DeepSeek-R1, ChatGPT-4o, and GPT-5) against partial least squares (PLS) regression for predicting Young's modulus (E), tensile strength (TS), and elongation at break (EL) based on pore diameter (PD), contact angle (CA), thickness (T), and porosity (P) measurements. These knowledge-driven approaches demonstrated property-specific advantages over the chemometric baseline. For EL, LLMs achieved statistically significant improvements, with DeepSeek-R1 and GPT-5 delivering 40.5% and 40.3% of Root Mean Square Error reductions, respectively, reducing mean absolute errors from $11.63\pm5.34$% to $5.18\pm0.17$%. Run-to-run variability was markedly compressed for LLMs ($\leq$3%) compared to PLS (up to 47%). E and TS predictions showed statistical parity between approaches ($q\geq0.05$), indicating sufficient performance of linear methods for properties with strong structure-property correlations. Error topology analysis revealed systematic regression-to-the-mean behavior dominated by data-regime effects rather than model-family limitations. These findings establish that LLMs excel for non-linear, constraint-sensitive properties under bootstrap instability, while PLS remains competitive for linear relationships requiring interpretable latent-variable decompositions. The demonstrated complementarity suggests hybrid architectures leveraging LLM-encoded knowledge within interpretable frameworks may optimise small-data materials discovery.