ReviewAngewandte Chemie (International ed. in English)2026
Accelerating Catalyst Materials Discovery With Large Artificial Intelligence Models.
Review in Angewandte Chemie (International ed. in English), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
3 citing papers in PubMed.
- Materials Databases: Foundations of Modern Digital Materials.Precision chemistry · 2026Review
- Balanced Electron Donation Governs Adsorption Site Selection in CO2 Electroreduction to HCOOH on Transition Metal-Doped Magnesium Oxides.The journal of physical chemistry letters · 2026Article
- A unified descriptor framework for hydrogen storage capacity and equilibrium pressure in interstitial hydrides.Chemical science · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
8 authors.
Funding
Abstract
The integration of artificial intelligence (AI) into catalysis is fundamentally reshaping the research paradigm of catalyst discovery. Unlike traditional trial-and-error approaches, AI-empowered data-driven technologies, particularly large AI models such as universal machine learning interatomic potentials (MLIPs) and large language models (LLMs), offer unprecedented capabilities in exploring complex spaces, predicting catalytic performance, and accelerating rational design. Standing at the forefront of data-driven science, we underscore how databases, universal MLIPs, and LLMs are revolutionizing the traditional catalysis paradigm and bridging the ontology-concept-computation-experiment continuum. We then demonstrate significant recent progress, and discuss their potential and challenges in the catalytic field. By leveraging cutting-edge universal MLIPs and LLMs, researchers can conduct large-scale simulations, highly efficient data acquisition, training, and prediction, and even self-directed research in the field of catalysis. Looking ahead, these advantages enable the rapid development of target catalysts, which will be propelled by integrated universal MLIPs, multimodal LLMs, and automation systems. Developments in these domains will pave the way toward AI-empowered closed-loop platforms and cross-disciplinary Digital Materials Ecosystems that broaden the discovery landscape and foster cross-materials innovation, marking the dawn of a new era in which catalyst materials discovery is perpetually accelerating.
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Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.