Morphological Heterogeneity Impact of Film Solid-State Cathode on Utilization and Fracture Dynamics
- Creators
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Park, Se Hwan1
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Juarez-Yescas, Carlos2
- Naik, Kaustubh G.3
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Wang, Yingjin4
- Luo, Yuting2
- Puthusseri, Dhanya1
- Kwon, Patrick2
- Vishnugopi, Bairav S.3
- Shyam, Badri5
- Yang, Heng5
- Cook, John5
- Okasinski, John6
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Chuang, Andrew C.6
- Xiao, Xianghui7
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Greer, Julia R.4
- Mukherjee, Partha P.3
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Zahiri, Beniamin2
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Braun, Paul V.2
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Hatzell, Kelsey B.1
Abstract
Structural heterogeneity in solid-state batteries can impact the material utilization and fracture mechanisms. Crystallographically oriented LiCoO2 film cathodes serve as a model electrode system for exploring how void distribution contributes to stress relief and buildup during cycling. Real- and reciprocal-space operando and ex situ synchrotron-based experiments are utilized to understand structural changes across multiple length scales that contribute to stress generation and fracture. Nanotomography uncovers a depth-dependent porosity variation in the pristine electrode and highlights the preferential fracture in regions of lower porosity during delithiation. Energy-dispersive X-ray diffraction and three-dimensional (3D) X-ray absorption near-edge spectroscopy (XANES) reveal the underutilization of cathode material in these regions. 3D XANES also confirms preferential delithiation near the subgrain boundaries. Chemo-mechanical modeling coupled with site-specific mechanical characterization demonstrates how stress accumulation in dense regions of the electrode leads to fracture and underutilization of active material. Our findings reveal the importance of material design to alleviate stress in small-volume changing cathodes.
Copyright and License
© 2025 American Chemical Society.
Supplemental Material
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Unit cell volume changes; modeled voltage profile; tomography characterization; schematic representation of sample preparation; EDXRD variation; and load–displacement data (PDF): nn5c06799_si_001.pdf (9.77 MB)
Acknowledgement
This work was supported by the Defense Advanced Research Projects Agency (DARPA) HR00112220028. This research used resources of the Advanced Photon Source, a U.S. Department of Energy (DOE) Office of Science user facility operated for the DOE Office of Science by Argonne National Laboratory under Contract No. DE-AC02-06CH11357. This research used resources 18-ID of the National Synchrotron Light Source II, a U.S. Department of Energy Office of Science User Facility operated for the DOE Office of Science by Brookhaven National Laboratory under Contract No. DE-SC0012704.
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Additional details
- Defense Advanced Research Projects Agency
- HR00112220028
- Available
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2025-06-04Published online
- Caltech groups
- Division of Engineering and Applied Science (EAS), Kavli Nanoscience Institute
- Publication Status
- In Press