Please use this identifier to cite or link to this item: https://doi.org/10.1016/S0013-4686(01)00452-2
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dc.titleLithium nickel oxyfluoride (Li1-zNi1+zFyO2-y) and lithium magnesium nickel oxide (Li1-z(MgxNi1-x)1+zO2) cathodes for lithium rechargeable batteries: II. Electrochemical investigations
dc.contributor.authorNaghash, A.R.
dc.contributor.authorLee, J.Y.
dc.date.accessioned2014-10-09T09:55:38Z
dc.date.available2014-10-09T09:55:38Z
dc.date.issued2001-04-30
dc.identifier.citationNaghash, A.R., Lee, J.Y. (2001-04-30). Lithium nickel oxyfluoride (Li1-zNi1+zFyO2-y) and lithium magnesium nickel oxide (Li1-z(MgxNi1-x)1+zO2) cathodes for lithium rechargeable batteries: II. Electrochemical investigations. Electrochimica Acta 46 (15) : 2293-2304. ScholarBank@NUS Repository. https://doi.org/10.1016/S0013-4686(01)00452-2
dc.identifier.issn00134686
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/92091
dc.description.abstractTwo series of Mg substituted and F substituted nickelates were prepared, among them Li1-zNi1+zFyO2-y (y = 0.015, z = 0.06) and Li1-z(MgxNi1-x)1+zO2 (x = 0.05, z = 0.08) have shown improved cycling performance compared to un-substituted LiNiO2. Cyclic voltametry (CV), quasi open circuit voltage (QOCV) measurements, and X-ray diffraction all indicate that phase transitions in the charge and discharge reactions are partially suppressed after F or Mg substitution. Excessive substitution, however, results in reduced capacity and the lack of electrochemical activity. For Li1-zNi1+zFyO2-y this is explained by the increasing presence of divalent nickel ions at the lithium 3b sites. For Li1-z(MgxNi1-x)1+zO2, the presence of Mg ions at the lithium sites is more likely the reason. © 2001 Elsevier Science Ltd.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1016/S0013-4686(01)00452-2
dc.sourceScopus
dc.subjectAnion substitution
dc.subjectCation substitution
dc.subjectFluorine and magnesium
dc.subjectLithium nickel oxide
dc.subjectLithium-ion battery
dc.typeArticle
dc.contributor.departmentCHEMICAL & ENVIRONMENTAL ENGINEERING
dc.description.doi10.1016/S0013-4686(01)00452-2
dc.description.sourcetitleElectrochimica Acta
dc.description.volume46
dc.description.issue15
dc.description.page2293-2304
dc.description.codenELCAA
dc.identifier.isiut000168422900001
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