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dc.contributor.advisorIrvine, John T. S.
dc.contributor.authorAzad, Atia
dc.coverage.spatial153en_US
dc.date.accessioned2023-12-12T16:17:19Z
dc.date.available2023-12-12T16:17:19Z
dc.date.issued2024-06-13
dc.identifier.urihttps://hdl.handle.net/10023/28857
dc.description.abstractSilicon is a promising negative electrode material for lithium-ion batteries because of its high specific capacity which is ten times higher than graphite. Lithium silicides are also the negative electrode material for thermal batteries. As a result, lithium silicides are of significant interest to the battery community. There are four thermodynamically stable phases in the lithium-silicon system: Li₂₁Si₅, Li₁₃Si₄, Li₇Si₃, Li₁₂Si₇ and this was determined electrochemically. The coulometric titration curve for lithium silicides was obtained at 415°C by Wen and Huggins. This work collected electrochemical data on lithium silicides as the negative electrode materials for thermal batteries before carrying out neutron diffraction on lithium-silicon phases. Galvanostatic discharges of FeS₂/LiCl-KCl/Li-Si cells were carried out to identify the voltage plateaux. Payne et al observed that no new lithium-silicon phases formed during the discharge of the thermal batteries with NiS₂/Li₁₃Si₄ and CoS₂/Li₁₃Si₄ chemistries. The question remained if a loss in crystallinity occurred due to Li₁₃Si₄ becoming amorphous during lithium removal at high temperature. This work studied if high temperature amorphisation occurs in Li₁₃Si₄ and Li₇Si₃ phases because electrochemically driven amorphisation was seen in the silicon electrode in lithium-ion cells at room temperature. The Li-Si phases were probed at room temperature and at high temperature (500°C). The thermal expansion coefficients were obtained from the neutron data. The samples retained crystallinity and did not become amorphous at high temperature. Both phases were remarkably stable at high temperature. The second part of this work studied the silicon clusters that exist within lithium silicides. The silicon clusters, which behave like molecules, likely control the electrochemistry of the batteries. Structural, magnetic and electronic transitions of the lithium silicides were investigated to find which temperature points to collect longer and good quality structural information with total scattering neutron diffraction.en_US
dc.description.sponsorshipThis work was supported by AWE. This work was also supported by the EPSRC Light Element Analysis Facility Grant EP/T019298/1 and the EPSRC Strategic Equipment Resource Grant EP/R023751/1 for funding the scanning electron microscopy instruments. —Funding
dc.language.isoenen_US
dc.relationStudies of Lithium-Silicon Negative Electrode Materials for Batteries (Thesis data). Azad, A. & Irvine, J. T. S., University of St Andrews. https://doi.org/10.17630/e44eae73-ca6e-4562-a9f6-0e06865174c1
dc.relation.urihttps://doi.org/10.17630/e44eae73-ca6e-4562-a9f6-0e06865174c1
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivatives 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectBatteryen_US
dc.subjectAnodeen_US
dc.subjectSiliconen_US
dc.subjectNegative electrodeen_US
dc.subjectLithium-siliconen_US
dc.subjectNeutron diffractionen_US
dc.subjectLithiumen_US
dc.subjectLithium silicideen_US
dc.subject.lccTK2945.L58A8
dc.subject.lcshLithium ion batteriesen
dc.subject.lcshSilicon--Electric propertiesen
dc.subject.lcshLithium silicatesen
dc.subject.lcshElectrodes--Materialsen
dc.subject.lcshNeutrons--Diffractionen
dc.titleStudies of lithium-silicon negative electrode materials for batteriesen_US
dc.typeThesisen_US
dc.contributor.sponsorAWEen_US
dc.contributor.sponsorEngineering and Physical Sciences Research Council (EPSRC)en_US
dc.type.qualificationlevelDoctoralen_US
dc.type.qualificationnamePhD Doctor of Philosophyen_US
dc.publisher.institutionThe University of St Andrewsen_US
dc.rights.embargodate2026-12-08
dc.rights.embargoreasonThesis restricted in accordance with University regulations. Restricted until 8 December 2026
dc.identifier.doihttps://doi.org/10.17630/sta/675
dc.identifier.grantnumberEP/T019298/1en_US
dc.identifier.grantnumberEP/R023751/1en_US


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    Except where otherwise noted within the work, this item's licence for re-use is described as Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International