1997
DOI: 10.1006/jssc.1997.7546
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Structural and Local Environment Modifications in a Chemically Lithiated Iron Thiospinel

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Cited by 10 publications
(8 citation statements)
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“…Similar behavior has been observed chemical lithium insertion (8). the Mo¨ssbauer results showing no reduction of Fe>, seems to indicate that the incoming electrons during the insertion process do not cause a net reduction of cations but an increase in covalency of the network (as deduced from Fe Mo¨ssbauer spectroscopy), the electrons being incorporated into the delocalized band structure.…”
Section: Structural Analysissupporting
confidence: 73%
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“…Similar behavior has been observed chemical lithium insertion (8). the Mo¨ssbauer results showing no reduction of Fe>, seems to indicate that the incoming electrons during the insertion process do not cause a net reduction of cations but an increase in covalency of the network (as deduced from Fe Mo¨ssbauer spectroscopy), the electrons being incorporated into the delocalized band structure.…”
Section: Structural Analysissupporting
confidence: 73%
“…Since these sites are close to each other (8a to 16c and 8b to 16d), an increase in electrostatic repulsions is expected. Other different cation distributions are possible, as we have recently shown (8), by occupying simultaneously 8a, 8b, 16c, and 16d sites. In all cases, the cations can be redistributed to minimize the repulsive interactions up to 8 Li/mol.…”
Section: Electrochemical Behaviormentioning
confidence: 94%
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“…However, there are very few reports on silver-based spinels. Among these, Ag 0.5 In 2.5 S 4 has been previously studied as a host lattice for lithium insertion by both chemical and electrochemical methods [13]. The quaternary silver-based spinel Ag 2 FeSn 3 S 8 has been earlier reported in the literature [14] and is isostructural with the copper analogue, Cu 2 FeSn 3 S 8 [15].…”
Section: Introductionmentioning
confidence: 97%