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dc.contributor.authorMiao, Jinghui
dc.contributor.authorThompson, Carl Vernette
dc.date.accessioned2020-12-19T00:21:01Z
dc.date.available2020-12-19T00:21:01Z
dc.date.issued2018-03
dc.date.submitted2018-02
dc.identifier.issn1945-7111
dc.identifier.urihttps://hdl.handle.net/1721.1/128867
dc.description.abstractThe mechanisms and kinetics of lithiation and delithiation of amorphous silicon were investigated using potentiostatic techniques and thin films of different thickness, with a focus on the initial lithiation process that occurs in the first cycle. In potentiostatic tests, distinct kinks were observed in the current vs. time curves, and the time at which the kink occurred increased for thicker films. This behavior can be explained using a model in which a sharp interface between an amorphous LixSi phase and Li-saturated amorphous Si propagates through the film. Using this model, the rate-limiting process was determined to be diffusion of Li in the LixSi phase rather than reaction at the lithiation front. The Li diffusivity in the lithiated phase was determined to be in the 10−13 cm2/s range, independent of film thickness above 135 nm. The thin-film potentiostatic technique used in this study should prove useful in investigation of the mechanisms and rate parameters for other phase transitions that occur during lithiation of silicon and for kinetic studies of other electrode materials. ©2018 The Author(s)en_US
dc.language.isoen
dc.publisherThe Electrochemical Societyen_US
dc.relation.isversionofhttps://dx.doi.org/10.1149/2.1011803JESen_US
dc.rightsCreative Commons Attribution 4.0 International licenseen_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_US
dc.sourceElectrochemical Society (ECS)en_US
dc.titleKinetic Study of the Initial Lithiation of Amorphous Silicon Thin Film Anodesen_US
dc.typeArticleen_US
dc.identifier.citationMiao, Jinghui and Carl V. Thompson, "Kinetic Study of the Initial Lithiation of Amorphous Silicon Thin Film Anodes." Journal of the Electrochemical Society 165, 3 (March 2018): A650-A656 doi. 10.1149/2.1011803jes ©2018 Authorsen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Materials Science and Engineeringen_US
dc.relation.journalJournal of the Electrochemical Societyen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2019-09-24T16:59:41Z
dspace.date.submission2019-09-24T16:59:42Z
mit.journal.volume165en_US
mit.journal.issue3en_US
mit.metadata.statusComplete


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