Mesoscale Interrogation Reveals Mechanistic Origins of Lithium Filaments along Grain Boundaries in Inorganic Solid Electrolytes

Bairav S. Vishnugopi, Marm B. Dixit, Feng Hao, Badri Shyam, John B. Cook, Kelsey B. Hatzell, Partha P. Mukherjee

Research output: Contribution to journalArticlepeer-review

49 Scopus citations

Abstract

Solid-state batteries (SSBs), utilizing a lithium metal anode, promise to deliver enhanced energy and power densities compared to conventional lithium-ion batteries. Penetration of lithium filaments through the solid-state electrolytes (SSEs) during electrodeposition poses major constraints on the safety and rate performance of SSBs. While microstructural attributes, especially grain boundaries (GBs) within the SSEs are considered preferential metal propagation pathways, the underlying mechanisms are not fully understood yet. Here, a comprehensive insight is presented into the mechanistic interactions at the mesoscale including the electrochemical-mechanical response of the GB-electrode junction and competing ion transport dynamics in the SSE. Depending on the GB transport characteristics, a highly non-uniform electrodeposition morphology consisting of either cavities or protrusions at the GB-electrode interface is identified. Mechanical stability analysis reveals localized strain ramps in the GB regions that can lead to brittle fracture of the SSE. For ionically less conductive GBs compared to the grains, a crack formation and void filling mechanism, triggered by the heterogeneous nature of electrochemical-mechanical interactions is delineated at the GB-electrode junction. Concurrently, in situ X-ray tomography of pristine and failed Li7La3Zr2O12 (LLZO) SSE samples confirm the presence of filamentous lithium penetration and validity of the proposed mesoscale failure mechanisms.

Original languageEnglish
Article number2102825
JournalAdvanced Energy Materials
Volume12
Issue number3
DOIs
StatePublished - Jan 20 2022
Externally publishedYes

Funding

P.P.M. acknowledges support in part from the National Science Foundation (award no.: 2041499) and the Alfred P. Sloan Foundation through a Scialog: Advanced Energy Storage award. K.B.H. and M.B.D. were supported by the National Science Foundation under grant No. 1727863 and 1847029. K.B.H. and M.B.D. acknowledge the Vanderbilt Institute of Nanoscience and Engineering (VINSE) for access to their shared characterization facilities. 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. P.P.M. acknowledges support in part from the National Science Foundation (award no.: 2041499) and the Alfred P. Sloan Foundation through a Scialog: Advanced Energy Storage award. K.B.H. and M.B.D. were supported by the National Science Foundation under grant No. 1727863 and 1847029. K.B.H. and M.B.D. acknowledge the Vanderbilt Institute of Nanoscience and Engineering (VINSE) for access to their shared characterization facilities. 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.

FundersFunder number
Vanderbilt Institute of Nanoscience and Engineering
National Science Foundation2041499
U.S. Department of Energy
Directorate for Engineering1847029, 1727863
Alfred P. Sloan Foundation
Office of Science
Argonne National LaboratoryDE‐AC02‐06CH11357

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