1996
DOI: 10.1006/jssc.1996.0067
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Chemical Extraction of Lithium from Layered LiCoO2

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Cited by 107 publications
(62 citation statements)
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(5 reference statements)
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“…This basal increment is a result of the increase in electrostatic repulsion between CoO 2 layers. [27] Such a slight lattice expansion upon acid treatment clearly demonstrates no intercalation of water molecules into the layered cobalt oxide lattice. This contrasts with the case of Na 0.7 CoO 2 , in which acid treatment leads to the formation of the BLH phase with expanded basal spacing (c = 10.08 ).…”
Section: Resultsmentioning
confidence: 98%
“…This basal increment is a result of the increase in electrostatic repulsion between CoO 2 layers. [27] Such a slight lattice expansion upon acid treatment clearly demonstrates no intercalation of water molecules into the layered cobalt oxide lattice. This contrasts with the case of Na 0.7 CoO 2 , in which acid treatment leads to the formation of the BLH phase with expanded basal spacing (c = 10.08 ).…”
Section: Resultsmentioning
confidence: 98%
“…The chemical extraction of lithium in aqueous medium was carried out at room temperature by stirring the oxide powders in 2.5 N H 2 SO 4 for 2 days, followed by filtering, washing with de-ionized water, and drying at 100 1C overnight in an air-oven. Extraction of lithium with aqueous acid is known to occur by a disproportionation of, for example, Mn 3+ into Mn 4+ (in solid) and Mn 2+ (into solution) in the spinel LiMn 2 O 4 [25] and Co 3+ into Co 4+ (in solid) and Co 2+ (into solution) in the layered LiCoO 2 [26].…”
Section: Methodsmentioning
confidence: 99%
“…The lithium atoms are located at the octahedral sites between the CoO 2 layers. After delithiation, lithium-deficient compounds Li x CoO 2 can be obtained [14][15][16]; this phase belongs to the same space group. It has also been found that the end member of these compounds, CoO 2, can be obtained by electrochemical de-intercalation [17][18][19].…”
Section: Introductionmentioning
confidence: 99%