Materials Discovery

This work discusses and tests the potential of reaction graphs for material synthesis, in which events consist of reaction steps (actions) and their outputs (observations). The importance comes from the requirement to synthesize technologically useful materials, especially those that are kinetically stabilized. Often, it is a science that follows years of trial and error, culminating in (published) successful recipes, but is truly driven by far more (unpublished) failures. The entry into the era of AI provides an opportunity to use learning algorithms to encode rules from multi-dimensional synthesis pathways, regardless of their technological usefulness, and to decode both forward prediction and inverse learning modes. The main incentive is to accelerate material discovery by generating a global knowledge base that can be shared among data agents and contributed to by them. We will focus on several scenarios in the common synthesis process during solid-state synthesis, primarily because these reactions are kinetic in nature and require closer monitoring and control of the reaction history.

Materials and chemical optimization must choose the next synthesis, characterization, or high-fidelity simulation from sequential observations under a limited budget. Large language models can use task knowledge to propose adjustments, but composing surrogates, acquisition functions, and search strategies is constrained by compatibility, parameter dependencies, and evidence requirements. We present Agentic-MatriBO, a capability-compiled agentic Bayesian optimization (BO) framework that represents BO components and selection conditions as composable capabilities. A language policy proposes BO recipes and candidate plans; a compiler checks proposals against the registered capability catalog; and a deterministic execution layer validates and commits candidates. Oracle observations are stored in research memory and inform later rounds. We compare Agentic-MatriBO with eight baselines on four offline finite candidate pools---COF, PCE10, Buchwald--Hartwig (BH), and Suzuki--Miyaura---using five seeds per condition; results are reported descriptively. Across the four tasks, Agentic-MatriBO has the best mean endpoint quality after orienting each objective so that higher is better. On COF, it reaches the tabulated optimum in all five seeds both in the end-to-end comparison and after shared initialization, where it also retains an advantage in cumulative quality. Its normalized area under the best-so-far quality curve during the BO stage (nAUC-BO) is substantially higher on COF, near parity with the best baseline on PCE10 and BH, and lower on Suzuki. COF ablations show that removing the capability compiler or evidence gate coincides with lower cumulative quality and fewer exact-optimum hits. The framework provides an inspectable interface for evidence-conditioned BO adaptation.

Generative models have the potential to accelerate inorganic materials discovery by enabling inverse design, but generating experimentally realisable crystals remains challenging. Oxidation states are widely used to assess the compositional validity of crystals and guide inorganic materials discovery. While existing generative models for crystals can generate materials with charge-neutral oxidation-state assignments, they poorly reproduce the distributions of oxidation states observed in synthesised materials. To address this limitation, we propose OxiGen, an oxidation-state-aware crystal diffusion model that explicitly represents oxidation states during generation. OxiGen enforces global charge neutrality by construction using a structured output layer with exact inference over a finite-state automaton. Empirically, OxiGen substantially improves oxidation-state fidelity, generates the highest rate of stable, unique, and novel crystals among evaluated methods, and maintains high compositional validity even under property conditioning.

Atomistic foundation models screen hypothetical crystals by thresholding predicted energies, an output that states neither how likely a candidate is to be stable nor whether more computation would change the decision. CrystalJev reads one forward pass of a frozen potential on the unrelaxed structure and returns calibrated probabilities, conformal guarantees and a rule for escalating candidates to relaxation or density-functional theory (DFT). Across 65 Matbench Discovery models, threshold calls hide cost assumptions, and ordering slower computation by its value for the decision, rather than by probability, recovers most of its benefit at a tenth of its cost. In a registered prospective test with 2,100 DFT calculations on ionic substitutions, forecasts calibrated on existing data over-stated the stable fraction of new candidates by 0.9--2.2 percentage points, because the population had shifted, not the labelling protocol; a few hundred labels from the new pool removed this bias more reliably than label-free corrections.

The discovery and development of advanced materials is a challenging process constrained by the high time and monetary costs of synthesis, processing, and characterization. The underlying design spaces can be enormous, often with multiple competing objectives. Bayesian optimization (BO) provides a principled approach for efficiently navigating such spaces, but most workflows rely on fixed exploration-exploitation policies that lack the capacity to adapt to shifting constraints in dynamic campaigns typical of self-driving laboratories. In this work, we develop a multi-objective BO framework for alloy design under resource constraints, benchmarking strategies for adaptive policy tuning at each iteration. Our evaluation covers a septenary refractory high-entropy alloy (RHEA) system focused on maximizing melting temperature and minimizing density, and an Fe-Co-Ni-based soft magnetic alloy system targeting saturation magnetization, coercivity, and hardness. We compare an exploitation-focused strategy, a fixed mixed exploratory/exploitative policy, and two distinct LLM-based adaptive strategies with different approaches to batch allocation and campaign signal interpretation, evaluated across baseline and mid-campaign resource event conditions including budget reductions, timeline cuts, and combined disruptions. Our results show that mixed allocation strategies accumulate substantially more mutual information than the exploitation-focused baseline at a proportionally smaller cost to hypervolume and optimization speed, with adaptive strategies outperforming a fixed-mixed allocation policy by adjusting their allocation in response to both evolving campaign statistics and resource constraints. These findings suggest that adaptive resource allocation offers a favorable tradeoff for materials discovery campaigns in reducing predictive uncertainty on Pareto-optimal compositions.

The discovery of novel inorganic materials drives technological breakthroughs in critical fields such as computing and energy storage. Generative AI has promised to accelerate the materials discovery pipeline, but state-of-the-art flow and diffusion models remain bottlenecked by the cost of proposing candidate materials. To address this, we introduce OMatG-flash, an all-atom flow map for inorganic crystal structure prediction (CSP) and de novo generation (DNG). OMatG-flash is a Pareto-optimal inference engine for materials, sampling candidate materials with an order of magnitude fewer inference steps and less wall-clock time than existing flow and diffusion models while demonstrating benchmark performance on par with the state-of-the-art. To enable post-training fine-tuning we apply Reinforce Adjoint Matching to flow maps, further improving match rates and RMSE on the unconditional CSP task. OMatG-flash showcases the potential of flow maps to accelerate generation of high-quality candidate inorganic materials and demonstrates a step forward in sample throughput necessary for data-hungry materials discovery workflows.

Scientific literature contains latent knowledge about materials behavior, but much of this knowledge is expressed through words, contexts, and recurring associations rather than explicit design principles. This raises a central question: how can large-scale scientific corpora be used for practical problems in materials discovery? Here, we present a literature-guided descriptor-based filtering framework for reducing composition search spaces. For a given performance metric, the framework selects two descriptors from a filtered vocabulary in a literature-trained word embedding model and uses the selected descriptors to construct a Pareto-based filter for candidate compositions. Across the evaluated performance metrics and composition search spaces, the framework filters out an average of 74.27% of the candidate compositions, with an average best-value error of 1.93% relative to experimental measurements. Compared with expert-chosen and random descriptors, our performance metric-dependent descriptors provide a more controlled balance between retained fraction and best-value error. These results show that literature-derived embeddings can support intuitive and reproducible filters for narrowing candidate composition spaces while preserving high-performing compositions.

Energy systems face converging pressures for security, affordability, resilience, and sustainability, creating a need for faster discovery of deployable energy materials. Here we introduce SCALE (Simulation-Calibrated Amortized Learning for Energy Materials), a physics-grounded, real-world-data-calibrated learning architecture that connects deterministic scientific operators, experimental calibration, expanded calibrated label generation, and transformer-scale inference. SCALE converts selected high-cost mechanistic computation and measured evidence into reusable models for rapid screening, ranking, inverse design, and active learning. We formulate the framework, identify ten method-based application regimes, and demonstrate SCALE for solid-state metal-hydride hydrogen-storage capacity prediction. In this implementation, a hydride phase-equilibrium capacity operator is calibrated against 381 measured ML-HydPARK capacity anchors and used to generate 5,000 candidate-condition-prototype teacher labels. A crystallographically anchored periodic-graph representation preserves atomic sites, periodic neighbor relationships, and local metal environments absent from formula-only encodings. An edge-biased graph transformer with 2.90 million parameters reproduces calibrated teacher labels with five-fold surrogate fidelity of MAE 0.0582 wt% H2, RMSE 0.0833 wt% H2, R2 = 0.9927, and Pearson r = 0.9963. Post hoc attention analysis suggests that SCALE learns chemically organized element groupings and metal-metal relationships consistent with established hydride chemistry, without chemistry-group labels as supervision. Once trained, SCALE shifts million-candidate evaluation from repeated deterministic workflow execution to batched learned inference, reducing per-candidate screening cost by approximately 10^7-10^8 while retaining links to simulation and experimental evidence.

Learning materials properties from scarce labels and unlabeled crystals is a central challenge for data-driven materials discovery. We present SemiMat, a controlled benchmark for semi-supervised materials property regression, and MatRank, a reliability-weighted objective for continuous pseudo-label uncertainty. SemiMat fixes labeled and unlabeled crystal inputs, graph-backbone interfaces, validation-only checkpoint selection, held-out test reporting, normalized MAE (NMAE), and method-rank summaries across six scarce-label tasks, four graph backbones, and five predefined split runs. MatRank builds pseudo-targets from labeled anchors, weights them by local reliability and weak-prediction agreement, trains weak and strong graph views consistently, and adds ranking signals so that unlabeled crystals shape both values and candidate order. Across the retained 24 backbone-task blocks, one fixed MatRank objective gives the lowest aggregate held-out test NMAE (0.896) and best average method rank (2.208). The component, OOD, and generated-pool diagnostics identify where the gain is reliable and where further screening evaluation remains necessary. Code is available at https://github.com/littlepeachs/SemiMat.

Early discovery of at least one valid design satisfying a target requirement is a central objective in failure-prone closed-loop inverse design. A natural batch baseline ranks candidates by a product-form marginal valid-hit score, but selecting the highest-ranked candidates independently can produce redundant recommendations under predictive uncertainty and waste the experiment budget. We introduce ARC-SC(Anchored Risk-Constrained Scenario Coverage), a batch acquisition method that preserves strong marginal candidates as anchors and allocates the remaining batch positions by maximizing complementary coverage over predictive target scenarios under a risk-support constraint. In frozen-oracle closed-loop simulations on superconductivity and JARVIS materials-property benchmarks, ARC-SC yields a statistically supported improvement in first-hit discovery and remains competitive with directionally favorable first-hit performance on more challenging design space. These results establish ARC-SC as a POF-anchored, scenario-aware batch strategy for improving early valid-target discovery under structured experimental failure.

The coordination of multi-scale tasks is an effective strategy for computational materials discovery, yet the repeated application of diverse algorithms and tools renders it challenging. We report MAESTRO, a large language model (LLM) agent system capable of executing the entire screening pipeline for metal-organic frameworks (MOFs). It processes a large body of MOF literature, links relevant publications to their crystal structures, and curates the results into a computation-ready database, which is then screened through a strategy of progressively increasing computational cost. The promising candidates identified for separation under wet flue gas conditions all originate from unrelated studies. By connecting the heterogeneous stages of computational materials discovery, the LLM-based agents of MAESTRO can operate across application domains and uncover high-performance materials that conventional screening approaches would be unlikely to consider.

Data-driven materials discovery interpolates more reliably than it extrapolates and seldom reaches new structure types. We present MatEvolve, an agentic-AI framework designing crystals, proposing each candidate with a stated rationale and testing it. The agent reasons in an interpretable language of motifs, writing each crystal as a motif profile that describes the recurring geometric patterns---the motifs---composing it. The motif profile serves not merely as a description of a material but as the medium for material design: the agent edits the profile and constructs a crystal from the modified one, and the most promising candidates are validated by first-principles calculation. Applied to the design of rare-earth-lean permanent magnets, MatEvolve---built on the state-of-the-art language model Claude Fable~5 without fine-tuning---reaches new structural prototypes more than three times as often as generative models under an equal validation budget, at a comparable on-target-magnet rate. Beyond design, analysing the discovered crystals' human-readable profiles reveals structure--property relationships.

Advanced materials discovery increasingly relies on machine learning and Bayesian optimization to explore large discrete design spaces under limited evaluation budgets. However, conventional Bayesian optimization (BO) can become inefficient as candidate spaces grow, often evaluating low-value regions before reaching informative areas. We propose an active-learning (AL)-guided adaptive search-space refinement framework combined with multi-objective BO to accelerate materials optimization while preserving Pareto-relevant regions. We evaluate the approach on CH4/N2 separation in covalent-organic frameworks and pressure-vessel design with material-direction stress components and thickness objectives. Results show that the AL-guided refinement reduces the candidate space by approximately half while preserving more than 99 percent of the original hypervolume. The reduced-space strategy improves early convergence and cumulative Pareto-front discovery from the BO, demonstrating efficient large-scale materials optimization across constrained autonomous materials discovery settings.

Autonomous laboratories automate experimental execution, but a campaign must also decide which recovery pathway merits optimization. We formulate this as a sequential decision problem with a discrete pathway-identification stage and a continuous within-pathway optimization stage under heterogeneous experimental costs. Our implementation, Coactive learning, combines a cost-sensitive Bayesian hypothesis-discrimination policy motivated by EC2 (Golovin et al., 2010) with Gaussian-process Bayesian optimization (Srinivas et al., 2010). Under explicitly stated assumptions, the expected spend of one fixed-budget campaign attempt is bounded by the expected pathway-identification cost plus the capped within-pathway optimization budget. We evaluate the method on synthetic benchmarks constrained by selected results reported for PNNL's CICERO selective-precipitation study (Ritchhart et al., 2026). The method performs comparably to an oracle-pathway Bayesian-optimization reference and to a strong split-plate baseline that discriminates pathways with its first plate, without receiving an oracle label for the correct pathway. It is given a candidate hypothesis space and a diagnostic likelihood model. On an NdFeB-inspired instance, it avoids the simulated penalty of a commit-first baseline that initially selects a plausible but inferior hydroxide pathway. This hypothetical wrong-first-commitment scenario is motivated by the hydroxide-oxalate performance contrast reported by CICERO. We characterize the sensitivity of these conclusions to the assumed cost model. The code and benchmark are open source.

Driven by high-throughput experimentation, computational modeling, and artificial intelligence (AI), materials data has expanded at an unprecedented rate. Conventional materials databases function only as passive repositories, archiving raw experimental records indiscriminately including both successful and failed data, without systematic value filtering or asset management. This creates a critical gap between massive data accumulation and actionable innovation, hindering the identification of high-potential materials and industrial translation. To address this bottleneck, we propose an industrialization-oriented Materials Bank, a dedicated valuefiltering and assetization layer that operates beyond traditional databases. It does not merely curate high-quality data but systematically elevates qualified candidates into standardized, upgradable materials assets via a multi-dimensional BankCard framework covering scientific validity, synthesis feasibility, application readiness, and industrial value. By unifying databases, AI models, automated experimentation, and multi-criteria assessment into a cohesive closed-loop ecosystem, the Materials Bank establishes a clear trajectory from data to knowledge, candidate, asset, and product. It serves not as an enhanced database or screening tool, but as a decision infrastructure bridging academic discovery and industrial demand, offering a scalable paradigm to accelerate AI-driven materials innovation and deliver tangible real-world impact.

Closed-loop materials discovery iterates between proposing candidate structures and evaluating their properties, and property evaluation dominates the cost. In the generative variant, a learned prior proposes candidate crystals and a property oracle scores them; we ask whether a cheap probabilistic surrogate can triage the generator's output, and what such a surrogate must do well. Across three architecturally distinct pretrained diffusion priors (MatterGen, CrystalFlow, ADiT) and two targets (room-temperature heat capacity and bulk modulus), we insert a Gaussian process acquisition gate between structure generation and the oracle in an RL-steered generative workflow. The gate matches or exceeds ungated fine-tuning of the generative model while capping oracle calls at a fixed per-cycle budget. Budget-matched ablations isolate the mechanism. At an identical four-call budget, ranking-based selection outperforms arbitrary selection, confirming that the gain comes from the surrogate's choice; the gate comes within $\sim$9% of exhaustive oracle spending at roughly one-fifth of the calls. A density-functional-theory check of the bulk-modulus discoveries confirms the learned oracle to within 2.5% on average and the surrogate's ranking of the generated structures at Spearman $ρ= 0.94$. A cross-factorial benchmark of surrogate performance spanning mechanical, electronic, and vibrational properties identifies pretrained ORB embeddings with a Gaussian process as the most reliable combination, which we adopt as the building blocks of the proposed workflow. The complete pipeline is released as open-source software.

Machine-learned interatomic potentials now enable efficient atomistic evaluation for interactive materials discovery, yet closed-loop crystal search methods remain fragmented across bespoke pipelines for editing, relaxation, scoring, constraints, and bookkeeping. We introduce SciVerseGym, a Gymnasium-compatible environment for sequential crystal discovery that frames crystal design as a Markov decision process. Agents observe an atomistic structure, apply chemically meaningful edits, and receive feedback from a configurable evaluator. SciVerseGym supports local and global actions, including elemental substitution, lattice perturbation, atomic displacement, vacancy creation, and atom insertion, along with configurable chemical spaces, structure pools, atomistic and graph-based observations, custom rewards, optional relaxation, and stability or phonon-related diagnostics. Each step applies an edit, evaluates the candidate using a machine-learned interatomic potential or any ASE-compatible calculator, and returns the standard (obs, reward, terminated, truncated, info) tuple. By decoupling agent logic from materials infrastructure, SciVerseGym provides an open, reproducible, and extensible testbed for reinforcement learning, Bayesian optimization, evolutionary search, and language-agent workflows in closed-loop crystal discovery. Code is available at: https://github.com/Bin-Cao/SciVerseGym.

Inverse materials design starts from target functionality and searches for structures that can realize it. Its value in closed-loop discovery depends not only on prediction performance, but also on whether expensive first-principles results are independently validated, provenance-recorded, and admitted as feedback only when evidence is sufficient. This is especially important for composite properties such as carrier mobility, where a final scalar value hides intermediate quantities, fit quality, convergence history, and workflow assumptions. Here we present InvDesMobility, a reliability-gated first-principles feedback framework that integrates multi-agent automated DFT, evidence stratification, generative structure proposal, acquisition ranking, and auditable release. Using 516 2DMatPedia-derived candidates, the workflow produced 280 QC-passed materials and 573 retained carrier-direction seed channels after channel-level reliability gating. These records were split into two feedback objects: relaxed structures updated the generative model, while retained mobility channels trained the acquisition model and set validation priority. Over multiple iterations, InvDesMobility screened 2.4 x 10^6 structures, submitted 102 candidates for DFT validation, and retained 86 reliability-gated generated channels across 41 formulas. Overall, the main contribution is not a fixed list of high-mobility materials, but a transferable feedback contract that makes closed-loop inverse design both useful and auditable when learning from expensive calculated properties. All source data, retained feedback records, and workflows are available at https://github.com/DreamLufei/invDesMobility, with an accompanying evidence website at https://dreamlufei.github.io/invDesMobility/.

Self-driving laboratories (SDLs), where artificial intelligence proposes subsequent experiments and robotic systems execute them, are rapidly becoming the vanguard of materials discovery. A critical bottleneck, however, lies in seamlessly bridging diverse AI algorithms tailored for specific exploration goals with the heterogeneous robotic hardware found across different laboratories. Here, we present NIMO, an open-source software platform designed to dissolve this barrier through three core paradigms: a modular AI-robot decoupling mediated via simple CSV file exchange, a discrete candidate-pool architecture that seamlessly absorbs domain knowledge, and a unified Python interface pre-loaded with twelve distinct AI algorithms. In this Perspective, we review the operational principles of each algorithm alongside six diverse SDL implementations driven by NIMO, covering electrolyte discovery, organic synthesis, thin-film exploration, fuel-cell process informatics, coffee-ring phase exploration, and legacy liquid-handling automation. One of these also demonstrates NIMO's seamless interoperability with the IvoryOS orchestration framework. To democratize autonomous science, we also introduce a no-code desktop application that enables intuitive, human-in-the-loop exploration for non-programmers. NIMO is freely available at https://github.com/NIMS-DA/nimo, offering a versatile, plug-and-play foundation to accelerate autonomous materials exploration across diverse experimental landscapes.

Autonomous labs enable the integration of automated experiment execution, data analysis and decision making. The main challenge remains the integration of diverse data streams from multiple instruments, where the data is often heterogeneous and unsynchronized. The standard learning process of undetermined synthesis-process-structure-property relationships (SPSPR) usually relies on post-experiment analysis after data is fully collected, not during live experiments, and decision making is carried out independently across characterization equipment. Here, we demonstrate the Multi-instrument Autonomous Discovery (MAD) framework -- combining structural property mapping and functional property optimization simultaneously in a closed-loop manner. As an example, we applied MAD to phase change memory (PCM) materials, and, in particular on the Mn-Sb-Te ternary, a previously unexplored materials system for PCM. A multi-output model is employed to merge data from x-ray diffraction (XRD) and electrical resistance measurements simultaneously through a co-regionalization kernel that models the relationship between them. The output probabilistic posterior and uncertainty quantification facilitate decision making with shared knowledge, while the goals are different across tasks. We aimed to maximize the knowledge of crystal structure distribution using non-negative matrix factorization (NMF), while in parallel, we find the composition with the maximum resistance value, an important figure of merit for PCM. Leveraging MAD, we found promising electrical PCMs and identified the SPSPR within 25 closed-loop iterations, corresponding to a seven-fold speed-up. The framework opens a new path of study in large-scale autonomous facilities, where future experiments can be run in parallel together, not independently.

Rapid identification of candidate materials with target properties has become a key task in materials science. Machine learning has emerged as an alternative to physics-based simulation, offering a faster and cheaper way to filter materials based on their stability and other target properties, reducing the number of candidates that reach the costly synthesis stage. Recently, Large Language Models (LLMs) have been applied to this role, but these models are parameter-heavy and computationally expensive both during training and at inference time, making them unsuitable for high-throughput tasks. This inefficiency stems from both the large over-parameterization of language models and the difficulty of framing material generation as a sequence learning problem. In this paper, we present PRISMat, a cost-effective, permutation-invariant model, which addresses these limitations. We show that PRISMat, despite taking less time for inference, is able to outperform LLMs in generating crystal slabs conditioned on critical materials' surface properties. In targeted material discovery, we achieve mean absolute errors of 0.188 eV/A$^2$ and 2.79 eV for cleavage energy and work function tasks, respectively, reducing the error of the next best model by 4$\times$.

De novo crystal generation, a central task in materials discovery, aims to generate crystals that are simultaneously valid, stable, unique, and novel. Existing methods mainly rely on black-box stochastic sampling, providing limited control over how generated structures move beyond the observed distribution. In this paper, we introduce a concept-based compositional framework for crystal generation. We train a vector-quantized variational autoencoder to automatically discover a shared set of reusable crystal concepts, which serve as building blocks for guided generation. These learned concepts naturally exhibit interpretability from both local atomic environments and global symmetry patterns, and generalize to crystals from different distributions. By recombining such concepts, our framework enables controllable exploration of novel crystals beyond the training distribution, rather than relying solely on unconstrained random sampling. To further improve composition efficiency, we introduce a composition generator and iteratively refine it using high-quality samples generated by the model itself. The resulting concept compositions are then used to condition downstream crystal generation. Numerical experiments on MP-20 and Alex-MP-20 show that compositing concepts separately increase base model up to 53.2% and 51.7% on V.S.U.N metric, with particular gains in novelty.

De novo crystal generation seeks to discover materials that are not merely realistic, but also stable and novel. However, most existing generative models are trained to maximize the likelihood of observed crystals, which encourages samples to stay close to known materials yet not necessarily align with the criteria that matter in discovery. Our empirical analysis shows that current crystal generative models exhibit a clear conflict between stability and novelty: samples near the observed distribution tend to retain stability but offer limited novelty, whereas samples farther from it often lose stability rapidly. This suggests that the useful region for discovering crystals that are both stable and novel is extremely narrow. To move beyond this limitation, we introduce Crys-JEPA, a joint embedding predictive architecture for crystals that learns an energy-aware latent space preserving formation-energy differences. In this space, stability assessment can be reformulated as an embedding-based comparison against accessible training crystals, reducing the reliance on expensive energy evaluation and task-specific external references. Building on Crys-JEPA, we further develop a screening-and-refinement pipeline that identifies promising generated crystals and reintroduces them to refine the generative model. On MP-20 and Alex-MP-20 datasets, we achieve improvements over baselines up to 53.8% and 72.7% on V.S.U.N. metric, respectively.

The most technologically consequential materials are often the rarest: they occupy narrow regions of chemical space, obey competing physical constraints, and appear only sparsely in existing databases. High-kappa dielectrics, high-Tc superconductors, and ferromagnetic insulators are to name a few. This scarcity fundamentally limits today's data-driven materials discovery, where machine-learning models excel at interpolation but struggle to generate genuinely new candidates. Here, we introduce DielecMIND, an artificial intelligence framework that reframes materials discovery as a reasoning-driven exploration instead of a database-screening problem. Using high-kappa dielectrics as a data-scarce and technologically stringent test case, DielecMIND combines large-language-model hypothesis generation for the first time with physics validated first-principles calculation to navigate chemical space beyond known compounds. Prior to our work, only 14 experimentally or computationally validated materials with kappa > 150 were known. Our framework discovers and validates 5 new such compounds, expanding this rare-materials class by a remarkable = 35% in a single study. Among them, we find that Ba2TiHfO6 exhibits a dielectric constant of 637, minimal loss at low optical frequencies, and stability up to 800 K. Beyond dielectrics, this work demonstrates a new paradigm for artificial-intelligence-guided discovery: one that generates a small number of physically grounded, experimentally plausible candidates yet measurably expands sparsely populated functional materials spaces. Thus, DielecMIND points toward a general strategy for discovering rare, high-impact functional materials where data scarcity has long constrained progress.

CO2 reduction requires efficient catalysts, yet materials discovery remains bottlenecked by 10-20 year development cycles requiring deep domain expertise. This paper demonstrates how large language models can assist the catalyst discovery process by helping researchers explore chemical spaces and interpret results when augmented with retrieval-based grounding. We introduce a retrieval-augmented generation framework that enables GPT-4 to navigate chemical space by accessing a database of 50,000+ known materials, adapting general-purpose language understanding for high-throughput materials design. Our approach generated over 250 catalyst candidates with an 82% thermodynamic stability rate while addressing multi-objective constraints: 68% achieved <$100/kg cost with metallic conductivity (band gap<0.1eV) and mechanical stability (B/G>1.75). The best-performing Fe0.2Co0.2Ni0.2Ir0.1Ru0.3 achieves 0.285V limiting potential (25$18/kg. Volcano plot analysis confirms that 78% of LLM-generated catalysts cluster near the theoretical activity optimum, while our system achieves 200x computational efficiency compared to traditional high-throughput screening. By demonstrating that retrieval-augmented generation can ground AI creativity in physical constraints without sacrificing exploration, this work demonstrates an approach where natural language interfaces can streamline materials discovery workflows, enabling researchers to explore chemical spaces more efficiently while the LLM assists in result interpretation and hypothesis generation.

Recent advances in deep learning inspired neural network-based approaches to computational materials discovery (CMD). A plethora of problems in this field involve finding materials that optimize a target property. Nevertheless, the increasingly popular generative modeling methods are ineffective at boldly exploring attractive regions of the materials space due to their maximum likelihood training. In this work, we offer an alternative CMD technique based on offline model-based optimization (MBO) that fuses direct optimization of a target material property into generation. To that end, we introduce a domain-specific model, dubbed CliqueFlowmer, that incorporates recent advances of clique-based MBO into transformer and flow generation. We validate this model's optimization abilities and show that materials it produces strongly outperform those from generative baselines. To support specialized materials discovery applications and broader interdisciplinary research, we release our code, model weights, and additional project resources at https://github.com/znowu/CliqueFlowmer, https://colab.research.google.com/drive/1usUg7zezFkcYHlm2MdYwZUNJXf_YkWnY?usp=sharing, and https://x.com/kuba_AI/status/2033382617442345321.

Machine learning can accelerate materials discovery. Models perform impressively on many benchmarks. However, strong benchmark performance does not imply that a model learned chemistry. I test a concrete alternative hypothesis: that property prediction can be driven by bibliographic confounding. Across five tasks spanning MOFs (thermal and solvent stability), perovskite solar cells (efficiency), batteries (capacity), and TADF emitters (emission wavelength), models trained on standard chemical descriptors predict author, journal, and publication year well above chance. When these predicted metadata ("bibliographic fingerprints") are used as the sole input to a second model, performance is sometimes competitive with conventional descriptor-based predictors. These results show that many datasets do not rule out non-chemical explanations of success. Progress requires routine falsification tests (e.g., group/time splits and metadata ablations), datasets designed to resist spurious correlations, and explicit separation of two goals: predictive utility versus evidence of chemical understanding.

Predicting which hypothetical inorganic crystals can be experimentally realized remains a central challenge in accelerating materials discovery. SyntheFormer is a positive-unlabeled framework that learns synthesizability directly from crystal structure, combining Fourier-transformed crystal properties (FTCP) representation with structure-aware feature extraction, Random-Forest feature selection, and a compact deep MLP classifier. The model is trained on historical data from 2011 through 2018 and evaluated prospectively on future years from 2019 to 2025, where the positive class constitutes only 1.02 percent of samples. Under this temporally separated evaluation, SyntheFormer achieves a test AUC of 0.735, AUPRC of 0.099 and 97.6 percent recall at 94.2 percent coverage with dual-threshold calibration. Direct prospective validation supports this result as two materials that were unlabeled at the time of data curation, Y6Fe(SiS7)2 and BaYb2F8, were assigned high SyntheFormer scores (0.961 and 0.753, respectively) and were subsequently reported experimentally. Crucially, the model recovers experimentally confirmed metastable compounds that lie far from the convex hull and simultaneously assigns low scores to many thermodynamically stable yet unsynthesized candidates, demonstrating that stability alone is insufficient to predict experimental attainability.

Novelty search (NS) aims to uncover diverse system behaviors through simulation or experiment without requiring a pre-specified scalar objective. This capability is especially relevant to modern discovery problems in chemistry, materials science, and molecular design, where researchers often seek broad coverage of attainable property space rather than a single optimum and where each evaluation may require a costly computation or experiment. For such expensive black-box settings, we propose BEACON, a sample-efficient NS strategy inspired by Bayesian optimization principles. BEACON models the input-to-outcome mapping using multi-output Gaussian processes and selects new inputs by scoring how far plausible posterior outcomes lie from a denoised archive of previously observed outcomes. This gives a distance-based novelty acquisition that accounts for predictive uncertainty and observational noise while operating directly in continuous outcome space, rather than requiring direct optimization over a discretized partition of behaviors. By leveraging efficient posterior sampling together with scalable high-dimensional Gaussian process models, the proposed framework can be extended to settings with large data sets and high-dimensional design variables. We demonstrate BEACON on established benchmark problems together with real-world case studies in materials and molecular discovery. Across these settings, BEACON consistently discovers broader sets of distinct behaviors than several competing baselines under limited evaluation budgets.