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Revealing Local Structures through Machine-Learning-Fused Multimodal Spectroscopy

  • Haili Jia
  • , Yiming Chen
  • , Gi Hyeok Lee
  • , Jacob Smith
  • , Miaofang Chi
  • , Wanli Yang
  • , Maria K.Y. Chan

Research output: Contribution to journalArticlepeer-review

Abstract

Atomistic structures of materials offer valuable insights into their functionality. Determining these structures remains a fundamental challenge in materials science, especially for systems with defects. While both experimental and computational methods exist, each has limitations in resolving nanoscale structures. Core-level spectroscopies, such as X-ray absorption (XAS) or electron energy-loss spectroscopies (EELS), have been used to determine the local bonding environment and structure of materials. Recently, machine learning (ML) methods have been applied to extract structural and bonding information from XAS/EELS data. However, frameworks relying solely on a single data stream, defined as characterization data derived from a single element using one technique, are often insufficient because multiple local environments can yield similar spectral features, making it challenging to differentiate between competing structural hypotheses. In this work, we address this challenge by integrating multimodal ab initio simulations, experimental data acquisition, and ML techniques for structure characterization. Our goal is to determine local structures and properties using EELS and XAS data from multiple elements and edges. To showcase our approach, we use various lithium nickel manganese cobalt (NMC) oxide compounds which are used for lithium ion batteries, including those with oxygen vacancies and antisite defects, as the sample material system. We successfully inferred local element content, ranging from lithium to transition metals, with quantitative agreement with experimental data. Beyond local element inference, we find that ML model based on multimodal spectroscopic data is able to determine whether local defects such as oxygen vacancy and antisites are present, a task which is impossible for single mode spectra or other experimental techniques. Furthermore, our framework is able to provide physical interpretability, bridging spectroscopy with the local atomic and electronic structures.

Original languageEnglish
Pages (from-to)4228-4240
Number of pages13
JournalACS Nano
Volume20
Issue number5
DOIs
StatePublished - Feb 10 2026

Funding

This work is funded by the Energy Storage Research Alliance “ESRA” (DE-AC02-06CH11357), an Energy Innovation Hub funded by the U.S. Department of Energy, Office of Science, Basic Energy Sciences. M.K.Y.C. acknowledges the support from the BES SUFD Early Career award. Work performed at the Center for Nanoscale Materials, a U.S. Department of Energy Office of Science User Facility, was supported by the U.S. DOE, Office of Basic Energy Sciences, under Contract No. DE-AC02-06CH11357. This research used resources of the National Energy Research Scientific Computing Center, a DOE Office of Science User Facility supported by the Office of Science of the U.S. Department of Energy under Contract No. DE-AC02-05CH11231. We gratefully acknowledge the computing resources provided on Bebop, a high-performance computing cluster operated by the Laboratory Computing Resource Center at Argonne National Laboratory. Soft X-ray experiments were performed at BL8.0.1 of the Advanced Light Source (ALS), a DOE Office of Science User Facility, under contract no. DE-AC02-05CH11231. G.H.L. acknowledge the support from the U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences program under Award Number DE-SC0024404.

Keywords

  • battery
  • core-level spectroscopy
  • defect
  • density functional theory
  • electron energy-loss spectroscopy
  • machine learning
  • multimodal

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