Abstract
Probing the solid/liquid interface of batteries operando/in situ with ambient pressure X-ray photoelectron spectroscopy (APXPS) using the dip-and-pull method remains a challenging endeavor due to spatial and temporal variations in liquid layer shape, thickness, and composition. Monitoring the electrochemical and topographical nature of the liquid edge where the interface is accessed is essential to correctly interpret interfacial spectra. In this work, a methodology combining experimental design and software-based data processing for interface probing is reported. This experimental methodology utilizes continuous motion during fixed-mode APXPS measurements by periodically scanning across the dry electrode and thick electrolyte regions to capture the transitional interface. Two software-based approaches for retrieving the interface spectra are evaluated. In an analysis of the intensity attenuation pattern of a unique electrode signal, interface spectra are recognized at the edge of the intensity transition from electrode to electrolyte. The second method utilizes peak positions for interface identification. Selected spectra with the same peak energies also exhibit the same chemical features, indicating the close correlations between the interface energetics and local chemical compositions. Further, topographical information can be extracted using scanning APXPS by translating spectral intensities into liquid thickness, creating a spectro-microscopic 3D image of the liquid edge region. In the examined systems, the thickness of a propylene carbonate electrolyte edge on both lithium cobalt oxide and gold WE surfaces exhibits a step-jump transition from the thin to thick liquid region. The liquid distribution is also shown to depend on the morphological and chemical nature of the electrode. The imaging provides a better understanding of the relationship between liquid distribution and probed interface features while validating the functionality of the setup.
| Original language | English |
|---|---|
| Pages (from-to) | 18460-18474 |
| Number of pages | 15 |
| Journal | ACS Applied Materials and Interfaces |
| Volume | 18 |
| Issue number | 12 |
| DOIs | |
| State | Published - Apr 1 2026 |
Funding
We thank Swedish Research Council (2020-04512, 2022-06076), STandUP for energy, EU Horizon 2020 innovation program (875527─HYDRA project), VINNOVA (2022-01173─SUSTBAT), and Compel initiative for funding the presented research. We acknowledge MAX IV Laboratory for the APXPS measurements conducted at the HIPPIE beamline under proposals 20250151, 20250875, 20231495, 20230767, and 20230036. Research conducted at MAX IV, a Swedish national user facility, is supported by the Swedish Research Council under contract 2018-07152, the Swedish Governmental Agency for Innovation Systems under contract 2018-04969, and Formas under contract 2019-02496. The LCO thin film WEs were made by KLB and GMV and supported by the US Department of Energy’s Energy Efficiency and Renewable Energy Program, Vehicle Technologies Office, under the United States-Germany research program led by Tien Duong and Simon Thompson. L.D. thanks the German Research Foundation (DFG) for funding under Project ID 390874152 (POLiS Cluster of Excellence). We acknowledge Myfab Uppsala for providing facilities and experimental support. Myfab is funded by the Swedish Research Council (2020-00207) as a national research infrastructure.
Keywords
- Li-ion batteries
- ambient pressure X-ray photoelectron spectroscopy
- data processing
- dip-and-pull
- operando
- solid/liquid interface
- spectro-microscopic imaging
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