{"id":{"repo_id":"waikato-masters","oai_identifier":"oai:researchcommons.waikato.ac.nz:10289/14790"},"canonical_url":"https://search.dev.ndltd.org/etd/waikato-masters/oai:researchcommons.waikato.ac.nz:10289/14790","repository":{"repo_id":"waikato-masters","name":"University Waikato","base_url":"https://researchcommons.waikato.ac.nz/server/oai/request"},"display":{"title":"Synthesis and properties of some doped lithium transition-metal phosphates","abstract":"Four structurally related materials; LiNiPO₄, LiCoPO₄, Li₃Fe₂(PO₄)₃ and Li₃V₂(PO₄)₃, were synthesised, characterised and evaluated as potential cathode materials for lithium secondary batteries. The materials were synthesized using mainly solid-state techniques. Structural characterisation was performed using powder XRD with Rietveld refinement and Raman spectroscopy. Results showed that the pure forms of LiNiPO₄, LiCoPO₄ and Li₃Fe₂(PO₄)₃ could be synthesised in air at various temperatures. Li₃V₂(PO₄)₃ required a reducing atmosphere of 2%H₂/98%N₂ to achieve phase purity. Attempts were made to substitute all four materials with aliovalent dopants. Li₃Fe₂(PO₄)₃ and Li₃V₂(PO₄)₃ underwent a phase change depending on dopant content to a higher ionic conducting phase. AC impedance spectroscopy was used to determine conductivity of the materials. In general the phosphates are poor conductors. There was a significant increase in conductivity when substituting the transition metal Ti⁴⁺ for M³⁺ in Li₃Fe₂(PO₄)₃ and Li₃V₂(PO₄)₃, and V³⁺ for Co²⁺ in LiCoPO₄. The four materials and their highest conducting doped analogues were evaluated as cathodes in coin type lithium cells to determine their viability in Li secondary batteries. LiCoPO₄ showed a first discharge capacity of 130 mAh/g at 4.6V, but could be cycled over only a limited number of charge-discharge cycles owing to electrolyte instability at the high oxidation potentials (>5V) required for full charge. LiNiPO₄ could not be charged at all to accessible voltages. Ti doped Li₃Fe₂(PO₄)₃ had a relatively low discharge capacity of 60 mAh/g. Li₃V₂(PO₄)₃ and Ti doped Li₃V₂(PO₄)₃ showed a discharge capacity of 130 and 110 mAh/g respectively, although the Ti doped Li₃V₂(PO₄)₃ showed better cycling characteristics. Therefore, although aliovalent doping could increase the total conductivity of the phosphate materials, the accessible capacities of these materials remained limited.","abstract_html":"Four structurally related materials; LiNiPO₄, LiCoPO₄, Li₃Fe₂(PO₄)₃ and Li₃V₂(PO₄)₃, were synthesised, characterised and evaluated as potential cathode materials for lithium secondary batteries. The materials were synthesized using mainly solid-state techniques. Structural characterisation was performed using powder XRD with Rietveld refinement and Raman spectroscopy. Results showed that the pure forms of LiNiPO₄, LiCoPO₄ and Li₃Fe₂(PO₄)₃ could be synthesised in air at various temperatures. Li₃V₂(PO₄)₃ required a reducing atmosphere of 2%H₂/98%N₂ to achieve phase purity. Attempts were made to substitute all four materials with aliovalent dopants. Li₃Fe₂(PO₄)₃ and Li₃V₂(PO₄)₃ underwent a phase change depending on dopant content to a higher ionic conducting phase. AC impedance spectroscopy was used to determine conductivity of the materials. In general the phosphates are poor conductors. There was a significant increase in conductivity when substituting the transition metal Ti⁴⁺ for M³⁺ in Li₃Fe₂(PO₄)₃ and Li₃V₂(PO₄)₃, and V³⁺ for Co²⁺ in LiCoPO₄. The four materials and their highest conducting doped analogues were evaluated as cathodes in coin type lithium cells to determine their viability in Li secondary batteries. LiCoPO₄ showed a first discharge capacity of 130 mAh/g at 4.6V, but could be cycled over only a limited number of charge-discharge cycles owing to electrolyte instability at the high oxidation potentials (>5V) required for full charge. LiNiPO₄ could not be charged at all to accessible voltages. Ti doped Li₃Fe₂(PO₄)₃ had a relatively low discharge capacity of 60 mAh/g. Li₃V₂(PO₄)₃ and Ti doped Li₃V₂(PO₄)₃ showed a discharge capacity of 130 and 110 mAh/g respectively, although the Ti doped Li₃V₂(PO₄)₃ showed better cycling characteristics. Therefore, although aliovalent doping could increase the total conductivity of the phosphate materials, the accessible capacities of these materials remained limited.","abstract_has_math":false,"creators":["Butt, Garrett Phillip"],"institution":"The University of Waikato","degree_name":null,"degree_level":null,"degree_discipline":null,"degree_department":null,"school":null,"contributors":[],"advisors":["Sammes, Nigel","Swan, Janis E."],"committee_chairs":[],"committee_members":[],"year":2000,"date_issued":"2000","date_published":"2000","updated_at":"2026-07-24T05:57:18Z","subjects":[],"languages":[],"rights":["All items in Research Commons are provided for private study and research purposes and are protected by copyright with all rights reserved unless otherwise indicated."],"rights_urls":["https://researchcommons.waikato.ac.nz/bitstreams/27a38715-f324-49b1-b7dc-0cf62217dd16/download"],"identifier_entries":[]},"links":{"outbound_url":null,"outbound_label":null,"outbound_source":null},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor.advisor","label":"Advisor","values":["Sammes, Nigel","Swan, Janis E."]},{"key":"dc:creator","label":"Author","values":["Butt, Garrett Phillip"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date.issued","label":"Date","values":["2000"]},{"key":"dc:publisher.institution","label":"Dc Publisher Institution","values":["The University of Waikato"]},{"key":"dc:relation.isreferencedby","label":"Dc Relation Isreferencedby","values":["https://hdl.handle.net/10289/14790"]},{"key":"dc:type","label":"Dc Type","values":["Thesis"]}]},{"id":"language_rights","label":"Language and Rights","entries":[{"key":"dc:rights","label":"Dc Rights","values":["https://researchcommons.waikato.ac.nz/bitstreams/27a38715-f324-49b1-b7dc-0cf62217dd16/download","All items in Research Commons are provided for private study and research purposes and are protected by copyright with all rights reserved unless otherwise indicated."]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier.uri","label":"Identifier URI","values":["https://researchcommons.waikato.ac.nz/bitstreams/e8048aa0-f5d6-412b-b807-3b16a44b43d9/download"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description.abstract","label":"Abstract","values":["Four structurally related materials; LiNiPO₄, LiCoPO₄, Li₃Fe₂(PO₄)₃ and Li₃V₂(PO₄)₃, were synthesised, characterised and evaluated as potential cathode materials for lithium secondary batteries. The materials were synthesized using mainly solid-state techniques. Structural characterisation was performed using powder XRD with Rietveld refinement and Raman spectroscopy. Results showed that the pure forms of LiNiPO₄, LiCoPO₄ and Li₃Fe₂(PO₄)₃ could be synthesised in air at various temperatures. Li₃V₂(PO₄)₃ required a reducing atmosphere of 2%H₂/98%N₂ to achieve phase purity. Attempts were made to substitute all four materials with aliovalent dopants. Li₃Fe₂(PO₄)₃ and Li₃V₂(PO₄)₃ underwent a phase change depending on dopant content to a higher ionic conducting phase. AC impedance spectroscopy was used to determine conductivity of the materials. In general the phosphates are poor conductors. There was a significant increase in conductivity when substituting the transition metal Ti⁴⁺ for M³⁺ in Li₃Fe₂(PO₄)₃ and Li₃V₂(PO₄)₃, and V³⁺ for Co²⁺ in LiCoPO₄. The four materials and their highest conducting doped analogues were evaluated as cathodes in coin type lithium cells to determine their viability in Li secondary batteries. LiCoPO₄ showed a first discharge capacity of 130 mAh/g at 4.6V, but could be cycled over only a limited number of charge-discharge cycles owing to electrolyte instability at the high oxidation potentials (>5V) required for full charge. LiNiPO₄ could not be charged at all to accessible voltages. Ti doped Li₃Fe₂(PO₄)₃ had a relatively low discharge capacity of 60 mAh/g. Li₃V₂(PO₄)₃ and Ti doped Li₃V₂(PO₄)₃ showed a discharge capacity of 130 and 110 mAh/g respectively, although the Ti doped Li₃V₂(PO₄)₃ showed better cycling characteristics. Therefore, although aliovalent doping could increase the total conductivity of the phosphate materials, the accessible capacities of these materials remained limited."]},{"key":"dc:format.checksum.md5","label":"Dc Format Checksum Md5","values":["027077e19b5f8f3d43774ce84fb0a7f9","e14202ab27e47ddb00d33097327ba050","25de946e681900301919654c01d731b5"]},{"key":"dc:title","label":"Title","values":["Synthesis and properties of some doped lithium transition-metal phosphates"]}]}],"canonical_facts":{"dc:contributor.advisor":["Sammes, Nigel","Swan, Janis E."],"dc:creator":["Butt, Garrett Phillip"],"dc:date.issued":["2000"],"dc:description.abstract":["Four structurally related materials; LiNiPO₄, LiCoPO₄, Li₃Fe₂(PO₄)₃ and Li₃V₂(PO₄)₃, were synthesised, characterised and evaluated as potential cathode materials for lithium secondary batteries. The materials were synthesized using mainly solid-state techniques. Structural characterisation was performed using powder XRD with Rietveld refinement and Raman spectroscopy. Results showed that the pure forms of LiNiPO₄, LiCoPO₄ and Li₃Fe₂(PO₄)₃ could be synthesised in air at various temperatures. Li₃V₂(PO₄)₃ required a reducing atmosphere of 2%H₂/98%N₂ to achieve phase purity. Attempts were made to substitute all four materials with aliovalent dopants. Li₃Fe₂(PO₄)₃ and Li₃V₂(PO₄)₃ underwent a phase change depending on dopant content to a higher ionic conducting phase. AC impedance spectroscopy was used to determine conductivity of the materials. In general the phosphates are poor conductors. There was a significant increase in conductivity when substituting the transition metal Ti⁴⁺ for M³⁺ in Li₃Fe₂(PO₄)₃ and Li₃V₂(PO₄)₃, and V³⁺ for Co²⁺ in LiCoPO₄. The four materials and their highest conducting doped analogues were evaluated as cathodes in coin type lithium cells to determine their viability in Li secondary batteries. LiCoPO₄ showed a first discharge capacity of 130 mAh/g at 4.6V, but could be cycled over only a limited number of charge-discharge cycles owing to electrolyte instability at the high oxidation potentials (>5V) required for full charge. LiNiPO₄ could not be charged at all to accessible voltages. Ti doped Li₃Fe₂(PO₄)₃ had a relatively low discharge capacity of 60 mAh/g. Li₃V₂(PO₄)₃ and Ti doped Li₃V₂(PO₄)₃ showed a discharge capacity of 130 and 110 mAh/g respectively, although the Ti doped Li₃V₂(PO₄)₃ showed better cycling characteristics. Therefore, although aliovalent doping could increase the total conductivity of the phosphate materials, the accessible capacities of these materials remained limited."],"dc:format.checksum.md5":["027077e19b5f8f3d43774ce84fb0a7f9","e14202ab27e47ddb00d33097327ba050","25de946e681900301919654c01d731b5"],"dc:identifier.uri":["https://researchcommons.waikato.ac.nz/bitstreams/e8048aa0-f5d6-412b-b807-3b16a44b43d9/download"],"dc:publisher.institution":["The University of Waikato"],"dc:relation.isreferencedby":["https://hdl.handle.net/10289/14790"],"dc:rights":["https://researchcommons.waikato.ac.nz/bitstreams/27a38715-f324-49b1-b7dc-0cf62217dd16/download","All items in Research Commons are provided for private study and research purposes and are protected by copyright with all rights reserved unless otherwise indicated."],"dc:title":["Synthesis and properties of some doped lithium transition-metal phosphates"],"dc:type":["Thesis"]},"updated_at":"2026-07-24T05:57:18Z"}