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dc.contributor.advisorBruce, Peter G.
dc.contributor.authorLyness, Christopher
dc.coverage.spatial238en_US
dc.date.accessioned2011-07-19T13:37:02Z
dc.date.available2011-07-19T13:37:02Z
dc.date.issued2011-06-22
dc.identifieruk.bl.ethos.552506
dc.identifier.urihttp://hdl.handle.net/10023/1921
dc.description.abstractTwo novel lithium host materials were investigated using structural and electrochemical analysis; the cathode material Li₂CoSiO₄ and the LiMO₂ class of anodes (where M is a transition metal ion). Li₂CoSiO₄ materials were produced utilising a combination of solid state and hydrothermal synthesis conditions. Three Li₂CoSiO₄ polymorphs were synthesised; β[subscript(I)], β[subscript(II)] and γ₀. The Li₂CoSiO₄ polymorphs formed structures based around a distorted Li₃PO₄ structure. The β[subscript(II)] material was indexed to a Pmn2₁ space group, the β[subscript(I)] polymorph to Pbn2₁ and the γ₀ material was indexed to the P2₁/n space group. A varying degree of cation mixing between lithium and cobalt sites was observed across the polymorphs. The β[subscript(II)] polymorph produced 210mAh/g of capacity on first charge, with a first discharge capacity of 67mAh/g. It was found that the β[subscript(I)] material converted to the β[subscript(II)] polymorph during first charge. The γ₀ polymorph showed almost negligible electrochemical performance. Capacity retention of all polymorphs was poor, diminishing significantly by the tenth cycle. The effect of mechanical milling and carbon coating upon β[subscript(II)], β[subscript(I)] and γ₀ materials was also investigated. Various Li[subscript(1+x)]V[subscript(1-x)]O₂ materials (where 0≤X≤0.2) were produced through solid state synthesis. LiVO₂ was found to convert to Li₂VO₂ on discharge, this process was found to be strongly dependent on the amount of excess lithium in the system. The Li₁.₀₈V₀.₉₂O₂ material had the highest first discharge capacity at 310mAh/g. It was found that the initial discharge consisted of several distinct electrochemical processes, connected by a complicated relationship, with significant irreversible capacity on first discharge. Several other LiMO₂ systems were investigated for their ability to convert to layered Li₂MO₂ structures on low voltage discharge. While LiCoO₂ failed to convert to a Li₂CoO₂ structure, LiMn₀.₅Ni₀.₅O₂ underwent an addition type reaction to form Li₂Mn₀.₅Ni₀.₅O₂. A previously unknown Li₂Ni[subscript(X)]Co[subscript(1-X)]O₂ structure was observed, identified during the discharge of LiNi₀.₃₃Co₀.₆₆O₂.en_US
dc.language.isoenen_US
dc.publisherUniversity of St Andrews
dc.subjectLithium-ionen_US
dc.subjectSilicate cathodeen_US
dc.subjectLiVO₂en_US
dc.subjectLi₂CoSiO₄en_US
dc.subjectTransition metal oxide anodeen_US
dc.subject.lccTK2945.L58L8
dc.subject.lccTK2945.L58L8
dc.subject.lcshLithium ion batteriesen_US
dc.subject.lcshCathodes--Materialsen_US
dc.subject.lcshAnodes--Materialsen_US
dc.subject.lcshLithium compoundsen_US
dc.subject.lcshTransition metal oxidesen_US
dc.titleNovel lithium-ion host materials for electrode applicationsen_US
dc.typeThesisen_US
dc.type.qualificationlevelDoctoralen_US
dc.type.qualificationnamePhD Doctor of Philosophyen_US
dc.publisher.institutionThe University of St Andrewsen_US


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