Li, X. ; Wei, Y. J. ; Ehrenberg, Helmut ; Du, F. ; Wang, C. Z. ; Chen, G. (2008)
Characterizations on the structural and electrochemical properties of LiNi1/3Mn1/3Co1/3O2 prepared by a wet-chemical process.
In: Solid State Ionics, 178 (39-40)
doi: 10.1016/j.ssi.2008.01.048
Artikel, Bibliographie
Kurzbeschreibung (Abstract)
LiNi1/3Mn1/3Co1/3O2 compounds were prepared at 700 (sample-A) and 900 °C (sample-B) by a simple wet-chemical process. X-ray diffraction showed the sample-A had a larger Li/Ni site exchange (9.9%) than that of the sample-B (4.4%). Raman scattering analysis suggests strong structural disorder within the octahedral [MO6] units due to different masses and bonding of the M–O bonds, as well as the Li/Ni site exchange in the crystals. The weakening of the Eg band was correlated with the Li/Ni site exchange. XPS analysis indicates that a lower annealing temperature than 900 °C leads to the formation of oxygen deficient LiNi1/3Mn1/3Co1/3O2 − δ. The electrochemical properties of the materials were investigated by charge–discharge experiments and electrochemical impedance spectroscopy. The drastic capacity fading of the sample-A was attributed to its structural properties. The sample-B showed satisfying cycling performance. But the capacity fading in the potential region of 2.5–4.6 V was larger than that in 2.5–4.4 V, which was attributed to the large charge transfer resistance at potentials above 4.4 V.
Typ des Eintrags: | Artikel |
---|---|
Erschienen: | 2008 |
Autor(en): | Li, X. ; Wei, Y. J. ; Ehrenberg, Helmut ; Du, F. ; Wang, C. Z. ; Chen, G. |
Art des Eintrags: | Bibliographie |
Titel: | Characterizations on the structural and electrochemical properties of LiNi1/3Mn1/3Co1/3O2 prepared by a wet-chemical process |
Sprache: | Englisch |
Publikationsjahr: | März 2008 |
Titel der Zeitschrift, Zeitung oder Schriftenreihe: | Solid State Ionics |
Jahrgang/Volume einer Zeitschrift: | 178 |
(Heft-)Nummer: | 39-40 |
DOI: | 10.1016/j.ssi.2008.01.048 |
Kurzbeschreibung (Abstract): | LiNi1/3Mn1/3Co1/3O2 compounds were prepared at 700 (sample-A) and 900 °C (sample-B) by a simple wet-chemical process. X-ray diffraction showed the sample-A had a larger Li/Ni site exchange (9.9%) than that of the sample-B (4.4%). Raman scattering analysis suggests strong structural disorder within the octahedral [MO6] units due to different masses and bonding of the M–O bonds, as well as the Li/Ni site exchange in the crystals. The weakening of the Eg band was correlated with the Li/Ni site exchange. XPS analysis indicates that a lower annealing temperature than 900 °C leads to the formation of oxygen deficient LiNi1/3Mn1/3Co1/3O2 − δ. The electrochemical properties of the materials were investigated by charge–discharge experiments and electrochemical impedance spectroscopy. The drastic capacity fading of the sample-A was attributed to its structural properties. The sample-B showed satisfying cycling performance. But the capacity fading in the potential region of 2.5–4.6 V was larger than that in 2.5–4.4 V, which was attributed to the large charge transfer resistance at potentials above 4.4 V. |
Freie Schlagworte: | Lithium–ion batteries; LiNi1/3Mn1/3Co1/3O2; X-ray diffraction; Raman scattering; Electrochemical properties |
Zusätzliche Informationen: | SFB 595 B4 |
Fachbereich(e)/-gebiet(e): | DFG-Sonderforschungsbereiche (inkl. Transregio) > Sonderforschungsbereiche > SFB 595: Elektrische Ermüdung > B - Charakterisierung > Teilprojekt B4: In situ Untersuchungen der Degradation von Interkalationsbatterien und deren Modellierung DFG-Sonderforschungsbereiche (inkl. Transregio) > Sonderforschungsbereiche > SFB 595: Elektrische Ermüdung > B - Charakterisierung DFG-Sonderforschungsbereiche (inkl. Transregio) > Sonderforschungsbereiche > SFB 595: Elektrische Ermüdung Zentrale Einrichtungen DFG-Sonderforschungsbereiche (inkl. Transregio) > Sonderforschungsbereiche DFG-Sonderforschungsbereiche (inkl. Transregio) |
Hinterlegungsdatum: | 15 Aug 2011 10:44 |
Letzte Änderung: | 05 Mär 2013 09:51 |
PPN: | |
Export: | |
Suche nach Titel in: | TUfind oder in Google |
Frage zum Eintrag |
Optionen (nur für Redakteure)
Redaktionelle Details anzeigen |