Deformation and Chemomechanical Degradation at Solid Electrolyte–Electrode Interfaces
Source abstract
Abstract
Solid electrolytes in batteries are inevitably subjected to mechanical strains when the active materials undergo chemically induced volume changes. It is difficult to probe these effects in complex battery structures. Thus, we developed a new in situ method to monitor mechanical deformation during electrochemical cycling, using simplified thin-film structures. This approach was applied to polymer electrolytes on V 2 O 5– x thin-film electrodes. Analysis of these deflection measurements was performed with a finite element model. The results indicate that the electrolyte compliance is rate-dependent and that it varies with the polymer molecular weight. Our approach was also employed to investigate interactions between chemical and mechanical changes at the solid electrolyte–electrode interface. Here, in situ stress studies were combined with impedance spectroscopy and ex situ peel tests. These results show that interfacial chemistry changes during electrochemical cycling lead to a significant decrease in the electrolyte–electrode adhesion energy.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advancements in Battery Materials · Advanced Battery Materials and Technologies · Conducting polymers and applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Engineering, Brown University, Providence, Rhode Island 02912, United States
Chemical Science and Engineering Division, Argonne National Laboratory, 9700 South Cass Avenue, Argonne, Illinois 60439-4837, United States
Medtronic Energy and Component Center, 6700 Shingle Creek Parkway, Brooklyn Center, Minnesota 55430, United States
Funding
Medtronic · Division of Materials Research
References (29)
Show source-provided references
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