Evidence map›Paper›PMID 40959384›Full record

ReviewChemical science2025

Machine learning for nonadiabatic molecular dynamics: best practices and recent progress.

Carolin Müller, Štěpán Sršeň, Brigitta Bachmair, Rachel Crespo-Otero, Jingbai Li, Sascha Mausenberger, Max Pinheiro, Graham Worth, Steven A Lopez, Julia Westermayr

Abstract readReview
In one paragraph

Review in Chemical science, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. The Newton-X platform for mixed quantum-classical dynamics.Physical chemistry chemical physics : PCCP · 2026
    Article
  2. Article
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Carolin MüllerComputer-Chemistry-Center, Friedrich-Alexander-Universität Erlangen-Nürnberg Nägelsbachstraße 25 91052 Erlangen Germany.ORCID https://orcid.org/0000-0002-5968-2216
Štěpán SršeňInstitute of Theoretical Chemistry, Faculty of Chemistry, University of Vienna Währinger Straße 17 1090 Wien Austria.ORCID https://orcid.org/0000-0001-7723-4540
Brigitta BachmairResearch Platform on Accelerating Photoreaction Discovery (ViRAPID), University of Vienna Währinger Straße 17 1090 Vienna Austria.ORCID https://orcid.org/0000-0002-2346-7995
Rachel Crespo-OteroDepartment of Chemistry, University College London 20 Gordon Street London WC1H 0AJ UK.ORCID https://orcid.org/0000-0002-8725-5350
Jingbai LiHoffmann Institute of Advanced Materials, Shenzhen Polytechnic University 7098 Liuxian Boulevard Shenzhen Guangdong 518055 P. R. China.ORCID https://orcid.org/0000-0003-4743-0318
Sascha MausenbergerInstitute of Theoretical Chemistry, Faculty of Chemistry, University of Vienna Währinger Straße 17 1090 Wien Austria.ORCID https://orcid.org/0009-0003-8136-8770
Max PinheiroAix Marseille University, CNRS, ICR Marseille France.ORCID https://orcid.org/0000-0002-5120-4172
Graham WorthDepartment of Chemistry, University College London 20 Gordon Street London WC1H 0AJ UK.ORCID https://orcid.org/0000-0002-2044-4499
Steven A LopezDepartment of Chemistry & Chemical Biology, Northeastern University 805 Columbus Avenue Boston MA 02120 USA s.lopez@northeastern.edu.ORCID https://orcid.org/0000-0002-8418-3638
Julia WestermayrWilhelm-Ostwald Institute, Leipzig Universityy Linnéstraße 2 04103 Leipzig Germany julia.westermayr@uni-leipzig.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Exploring molecular excited states holds immense significance across organic chemistry, chemical biology, and materials science. Understanding the photophysical properties of molecular chromophores is crucial for designing nature-inspired functional molecules, with applications ranging from photosynthesis to pharmaceuticals. Non-adiabatic molecular dynamics simulations are powerful tools to investigate the photochemistry of molecules and materials, but demand extensive computing resources, especially for complex molecules and environments. To address these challenges, the integration of machine learning has emerged. Machine learning algorithms can be used to analyse vast datasets and accelerate discoveries by identifying relationships between geometrical features and ground as well as excited-state properties. However, challenges persist, including the acquisition of accurate excited-state data and managing the complexity of the data. This article provides an overview of recent and best practices in machine learning for non-adiabatic molecular dynamics, focusing on pre-processing, surface fitting, and post-processing of data.

Identifiers

PMID40959384
PMCPMC12434613

What OpenQuestion holds

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Registered trials

None linked

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.