Electrochemical Stability of Li10GeP2S12 and Li7La3Zr2O12 Solid Electrolytes
Abstract
The electrochemical stability window of solid electrolyte is overestimated by the conventional experimental method using a Li/electrolyte/inert metal semiblocking electrode because of the limited contact area between solid electrolyte and inert metal. Since the battery is cycled in the overestimated stability window, the decomposition of the solid electrolyte at the interfaces occurs but has been ignored as a cause for high interfacial resistances in previous studies, limiting the performance improvement of the bulk-type solid-state battery despite the decades of research efforts. Thus, there is an urgent need to identify the intrinsic stability window of the solid electrolyte. The thermodynamic electrochemical stability window of solid electrolytes is calculated using first principles computation methods, and an experimental method is developed to measure the intrinsic electrochemical stability window of solid electrolytes using a Li/electrolyte/electrolyte-carbon cell. The most promising solid electrolytes, Li10GeP2S12 and cubic Li-garnet Li7La3Zr2O12, are chosen as the model materials for sulfide and oxide solid electrolytes, respectively. The results provide valuable insights to address the most challenging problems of the interfacial stability and resistance in high-performance solid-state batteries.
- Authors:
-
- Univ. of Maryland, College Park, MD (United States). Dept. of Chemical and Biomolecular Engineering
- Univ. of Maryland, College Park, MD (United States). Dept. of Materials Science and Engineering
- Publication Date:
- Research Org.:
- Univ. of Maryland, College Park, MD (United States)
- Sponsoring Org.:
- USDOE Office of Energy Efficiency and Renewable Energy (EERE), Vehicle Technologies Office (EE-3V); National Science Foundation (NSF); US Army Research Office (ARO)
- OSTI Identifier:
- 1433676
- Alternate Identifier(s):
- OSTI ID: 1433674
- Grant/Contract Number:
- EE0006860; 1235719; TG-DMR130142; W911NF1510187
- Resource Type:
- Accepted Manuscript
- Journal Name:
- Advanced Energy Materials
- Additional Journal Information:
- Journal Volume: 6; Journal Issue: 8; Journal ID: ISSN 1614-6832
- Publisher:
- Wiley
- Country of Publication:
- United States
- Language:
- English
- Subject:
- 25 ENERGY STORAGE; all-solid-state batteries; electrochemical stability windows; first-principles computation; interfaces; solid electrolytes
Citation Formats
Han, Fudong, Zhu, Yizhou, He, Xingfeng, Mo, Yifei, and Wang, Chunsheng. Electrochemical Stability of Li10GeP2S12 and Li7La3Zr2O12 Solid Electrolytes. United States: N. p., 2016.
Web. doi:10.1002/aenm.201501590.
Han, Fudong, Zhu, Yizhou, He, Xingfeng, Mo, Yifei, & Wang, Chunsheng. Electrochemical Stability of Li10GeP2S12 and Li7La3Zr2O12 Solid Electrolytes. United States. https://doi.org/10.1002/aenm.201501590
Han, Fudong, Zhu, Yizhou, He, Xingfeng, Mo, Yifei, and Wang, Chunsheng. Thu .
"Electrochemical Stability of Li10GeP2S12 and Li7La3Zr2O12 Solid Electrolytes". United States. https://doi.org/10.1002/aenm.201501590. https://www.osti.gov/servlets/purl/1433676.
@article{osti_1433676,
title = {Electrochemical Stability of Li10GeP2S12 and Li7La3Zr2O12 Solid Electrolytes},
author = {Han, Fudong and Zhu, Yizhou and He, Xingfeng and Mo, Yifei and Wang, Chunsheng},
abstractNote = {The electrochemical stability window of solid electrolyte is overestimated by the conventional experimental method using a Li/electrolyte/inert metal semiblocking electrode because of the limited contact area between solid electrolyte and inert metal. Since the battery is cycled in the overestimated stability window, the decomposition of the solid electrolyte at the interfaces occurs but has been ignored as a cause for high interfacial resistances in previous studies, limiting the performance improvement of the bulk-type solid-state battery despite the decades of research efforts. Thus, there is an urgent need to identify the intrinsic stability window of the solid electrolyte. The thermodynamic electrochemical stability window of solid electrolytes is calculated using first principles computation methods, and an experimental method is developed to measure the intrinsic electrochemical stability window of solid electrolytes using a Li/electrolyte/electrolyte-carbon cell. The most promising solid electrolytes, Li10GeP2S12 and cubic Li-garnet Li7La3Zr2O12, are chosen as the model materials for sulfide and oxide solid electrolytes, respectively. The results provide valuable insights to address the most challenging problems of the interfacial stability and resistance in high-performance solid-state batteries.},
doi = {10.1002/aenm.201501590},
journal = {Advanced Energy Materials},
number = 8,
volume = 6,
place = {United States},
year = {Thu Jan 21 00:00:00 EST 2016},
month = {Thu Jan 21 00:00:00 EST 2016}
}
Web of Science
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Sulfur Redox Reactions at Working Interfaces in Lithium-Sulfur Batteries: A Perspective
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Engineering the conductive carbon/PEO interface to stabilize solid polymer electrolytes for all-solid-state high voltage LiCoO 2 batteries
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Strategies Based on Nitride Materials Chemistry to Stabilize Li Metal Anode
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A Crosslinked Polyethyleneglycol Solid Electrolyte Dissolving Lithium Bis(trifluoromethylsulfonyl)imide for Rechargeable Lithium Batteries
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