人工知能によりX線分光法を5倍高速化・高精度化(Artificial intelligence makes X-ray spectroscopy five times faster, smarter and less prone to human error)

2026-03-02 アルゴンヌ国立研究所(ANL)

米国のArgonne National Laboratoryの研究チームは、人工知能(AI)を用いてX線分光法の実験プロセスを大幅に高速化・高精度化する新手法を開発した。従来のX線分光では測定やデータ解釈に熟練技術者の介入が必要であったが、このAI駆動型アプローチは必要な測定数を最大80%削減しつつ、ヒューマンエラーを低減し、全体の処理速度を約5倍に向上させることに成功した。AIモデルはスペクトルデータの取得と分析をリアルタイムで補助し、ノイズや不要なデータに対する頑健性も高めるため、複雑な試料評価や物質特性解析の効率を格段に上げる。これにより、材料科学・化学・物質解析など幅広い分野でのX線分光技術の実用性とスループットが飛躍的に向上すると期待されている。こうした自動化・AI統合は、研究と産業の両面で実験時間とコストの削減に寄与する。

人工知能によりX線分光法を5倍高速化・高精度化(Artificial intelligence makes X-ray spectroscopy five times faster, smarter and less prone to human error)
Artistic rendering shows new AI-guided approach capturing absorption edge from atomic structure of material analyzed by XANES at a light source. (Image by Argonne National Laboratory.)

<関連情報>

動的X線分光法のためのAI駆動型ワークフローのデモンストレーション Demonstration of an AI-driven workflow for dynamic x-ray spectroscopy

Ming Du,Mark Wolfman,Chengjun Sun,Shelly D. Kelly & Mathew J. Cherukara
npj Computational Materials  27 October 2025
DOI:https://doi.org/10.1038/s41524-025-01771-7

Abstract

X-ray absorption near edge structure (XANES) spectroscopy is a powerful technique for characterizing the chemical state and symmetry of individual elements within materials, but requires collecting data at many energy points which can be time-consuming. While adaptive sampling methods exist for efficiently collecting spectroscopic data, they often lack domain-specific knowledge about the structure of XANES spectra. Here we demonstrate a knowledge-injected Bayesian optimization approach for adaptive XANES data collection that incorporates understanding of spectral features like absorption edges and pre-edge peaks. We show this method accurately reconstructs the absorption edge of XANES spectra using only 15–20% of the measurement points typically needed for conventional sampling, while maintaining the ability to determine the x-ray energy of the sharp peak after the absorption edge with errors less than 0.03 eV, the absorption edge with errors less than 0.1 eV; and overall root-mean-square errors less than 0.005 compared to traditionally sampled spectra. Our experiments on battery materials and catalysts demonstrate the method’s effectiveness for both static and dynamic XANES measurements, improving data collection efficiency and enabling better time resolution for tracking chemical changes. This approach advances the degree of automation in XANES experiments, reducing the common errors of under- or over-sampling points near the absorption edge and enabling dynamic experiments that require high temporal resolution or limited measurement time.

1701物理及び化学
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