{
  "abstract": "Machine-learned interatomic potentials (MLIPs) deliver near-quantum-mechanical accuracy at a fraction of the computational cost. Their performance depends on the quality and composition of the training data: the training set must cover the range of atomic environments the model will encounter, yet unnecessary redundancy increases training cost without improving accuracy and can inadvertently introduce training biases. Dataset pruning (i.e., selecting a compact, representative subset from a larger collection) has emerged as a practical strategy for building high-quality training sets. Recently, methods based on informationtheoretic diversity measures such as QUESTS (Quick Uncertainty and Entropy from STructural Similarity) have shown significant promise, however, QUESTS requires specification of a lengthscale parameter (kernel bandwidth) that controls how similar two atomic environments must be before one is considered redundant. We show that operationally useful values of this parameter vary across structurally distinct phases, making naive automated pruning of heterogeneous datasets challenging. We present a pruning framework that addresses this problem by adapting the bandwidth independently for distinct thermodynamic subsets of the training dataset using an automatable elbow criterion applied to QUESTS informationentropy metrics. Farthest-point sampling (FPS) is then applied within each group to select maximally diverse atomic environments. Using the Small Carbon ChIMES 2.0 dataset comprising diamond, graphite, and liquid carbon spanning a broad range of thermodynamic conditions, we show that use of a single global bandwidth yields pruned datasets that can be strongly dominated by a single phase, particularly when the distribution of environments varies significantly between phases (e.g., liquid vs crystalline).1,2 Relative to global pruning at the same retained fraction, group-aware adaptive pruning reduces test force-MAE by up to 37% for diamond and 26% for graphite for models trained on only 5% of the original training data, with corresponding improvements in radial distribution function (RDF) fidelity. Benefits are smaller in structurally heterogeneous conditions where a single thermodynamic label encompasses multiple distinct local bonding environments with different characteristic length scales, indicating that finer grouping is the natural remedy in such regimes. Across crystalline conditions, the elbow-selected bandwidth aligns with the onset of rapid error growth as the dataset is pruned, providing a practical, model-agnostic guide for pruning decisions that requires no model training.",
  "abstract_shown": true,
  "affiliations": [
    "Department of Chemical Engineering, University of Michigan, 500 S State St, Ann Arbor, MI, USA, 48109",
    "Materials Science Division",
    "Lawrence Livermore National Laboratory"
  ],
  "article_type": null,
  "arxiv": null,
  "author_total": 6,
  "authors": [
    {
      "affs": [
        0
      ],
      "name": "Benjamin R. Laubach",
      "orcid": "0009-0005-6862-958X"
    },
    {
      "affs": [
        1,
        2
      ],
      "name": "Joshua A. Vita"
    },
    {
      "affs": [
        1,
        2
      ],
      "name": "Kyle Bushick",
      "orcid": "0000-0003-2089-1296"
    },
    {
      "affs": [
        1,
        2
      ],
      "name": "Logan Williams",
      "orcid": "0000-0002-9062-8293"
    },
    {
      "affs": [
        1,
        2
      ],
      "name": "Vincenzo Lordi",
      "orcid": "0000-0003-2415-4656"
    },
    {
      "affs": [
        0
      ],
      "name": "Rebecca K. Lindsey",
      "orcid": "0000-0002-3438-9064"
    }
  ],
  "bibtex": "https://research.draconitic.com/paper/anzaqcerdx69y.bib",
  "cited_by": 0,
  "doi": "10.26434/chemrxiv.15008542/v1",
  "fulltext_url": null,
  "id": "anzaqcerdx69y",
  "issns": [],
  "landing_url": "https://chemrxiv.org/doi/full/10.26434/chemrxiv.15008542/v1",
  "language": null,
  "licence": "CC-BY",
  "licence_label": "CC BY",
  "licence_source": "journal",
  "licence_url": "https://creativecommons.org/licenses/by/4.0/",
  "metadata_licence": null,
  "native_subjects": [
    [
      "openalex",
      "2505|Machine Learning in Materials Science"
    ]
  ],
  "openalex": "W7212017246",
  "pdf_url": "https://chemrxiv.org/doi/pdf/10.26434/chemrxiv.15008542/v1",
  "pmcid": null,
  "pmid": null,
  "published": "2026-09-09",
  "publisher": "American Chemical Society (ACS)",
  "ris": "https://research.draconitic.com/paper/anzaqcerdx69y.ris",
  "sources": [
    {
      "first_seen": "2026-10-30T12:17:19Z",
      "native_id": "10.26434/chemrxiv.15008542",
      "source": "chemrxiv",
      "url": "https://chemrxiv.org/doi/full/10.26434/chemrxiv.15008542/v1"
    }
  ],
  "subjects": [
    {
      "field": "chemistry",
      "origin": "openalex:2505|Machine Learning in Materials Science",
      "subfield": "materials-polymers"
    }
  ],
  "title": "Entropy-Guided Dataset Reduction for Machine-Learned Interatomic Potentials",
  "title_text": "Entropy-Guided Dataset Reduction for Machine-Learned Interatomic Potentials",
  "type": "preprint",
  "updated_at": "2026-10-30T12:17:19Z",
  "url": "https://research.draconitic.com/paper/anzaqcerdx69y",
  "venue": "ChemRxiv",
  "versions": []
}