Synthesis, electrochemistry and transition metal-doping of monoclinic Li4Ti5O12 and Na4Ti5O12
Field | Value | Language |
dc.contributor.author | Naeyaert, Pierre J P | |
dc.contributor.author | Avdeev, Maxim | |
dc.contributor.author | Ling, Chris D | |
dc.date.accessioned | 2022-07-20T05:59:07Z | |
dc.date.available | 2022-07-20T05:59:07Z | |
dc.date.issued | 2020 | en_AU |
dc.identifier.uri | https://hdl.handle.net/2123/29275 | |
dc.description.abstract | A new candidate Li-ion battery anode material, monoclinic M-Li4Ti5O12, has been prepared for the first time by ion-exchange from monoclinic M-Na4Ti5O12, and found to offer a stable electrochemical performance at rates of C/20 and 2C. The structural and electrochemical effects of transition metal M(III) doping of M-Na4Ti5O12 and Li4Ti5O12 have also been investigated. Doping was found to: facilitate the synthesis of the M-Na4Ti5O12 type structure, eliminating the need for strongly reducing conditions; increase the Na-ion content; and improve the stability in atmospheric conditions. Neutron powder diffraction and ex situ X-ray powder diffraction data collected at various points during electrochemical cycling reveal that phase changes in Li4Ti5O12 proceed via a two-phase mechanism, in contrast to M-Na4Ti5O12 which proceeds via a solid-solution mechanism. | en_AU |
dc.language.iso | en | en_AU |
dc.publisher | Elsevier | en_AU |
dc.relation.ispartof | Solid State Ionics | en_AU |
dc.rights | Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 | en_AU |
dc.title | Synthesis, electrochemistry and transition metal-doping of monoclinic Li4Ti5O12 and Na4Ti5O12 | en_AU |
dc.type | Article | en_AU |
dc.subject.asrc | 0302 Inorganic Chemistry | en_AU |
dc.identifier.doi | 10.1016/j.ssi.2020.115375 | |
dc.type.pubtype | Author accepted manuscript | en_AU |
dc.relation.arc | DP170100269 | |
usyd.faculty | SeS faculties schools::Faculty of Science::School of Chemistry | en_AU |
usyd.citation.volume | 353 | en_AU |
usyd.citation.spage | 115375 | en_AU |
workflow.metadata.only | No | en_AU |
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