Lithium ion mobility in lithium intercalated interstitially stabilized yttrium monochloride, LizYClZx (Z = H, C, O)

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OriginalspracheEnglisch
Seiten (von - bis)265-271
Seitenumfang7
FachzeitschriftSOLID STATE IONICS
Jahrgang62
Ausgabenummer3-4
PublikationsstatusVeröffentlicht - Aug. 1993

Abstract

Regions of homogeneity were determined for the systems LizYClHx, LizYCLCx and LizYCLOx. Cell parameters for the different samples are given and trends, especially for the length of the c axis, are discussed. Temperature dependent Guinier-Simon investigations on different LizYClHx compounds show a shortening of the c axis at 480°C, which must be interpreted as a deintercalation of lithium. Y2Cl3 forms upon decomposition of LizYClHx at 1100°C. Conductivity measurements on a pellet of 7Li0.15YClD0.65 give a specific resistance of 2.2 × 10-1 ω·cm at 298 K which hints at electronic conductivity. Cell parameters, atomic positional parameters and occupation factors gained from a neutron powder diffraction experiment on 7Li0.15YClD0.65 are reported. The line shape of 7Li-NMR powder spectra is consistent with lithium at a definite lattice site. For all samples motional narrowing starts below room temperature. In the system LizYClC0.5 pronounced diffusion induced peaks of the spin-lattice relaxation rate T-11(T) of 7Li are observed above room temperature which exhibit the temperature dependence typical of disordered systems. In Li0.15YClD0.65 the 7Li spin-lattice relaxation rate, at the applied field of 4.7 T, does not show a significant peak but a continuous increase with temperature in the range from 150 K to 800 K.

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Lithium ion mobility in lithium intercalated interstitially stabilized yttrium monochloride, LizYClZx (Z = H, C, O). / Mattfeld, Heiner; Balzer-Jöllenbeck, Gert; Meyer, Gerd et al.
in: SOLID STATE IONICS, Jahrgang 62, Nr. 3-4, 08.1993, S. 265-271.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Mattfeld H, Balzer-Jöllenbeck G, Meyer G, Heitjans P. Lithium ion mobility in lithium intercalated interstitially stabilized yttrium monochloride, LizYClZx (Z = H, C, O). SOLID STATE IONICS. 1993 Aug;62(3-4):265-271. doi: 10.1016/0167-2738(93)90381-C
Mattfeld, Heiner ; Balzer-Jöllenbeck, Gert ; Meyer, Gerd et al. / Lithium ion mobility in lithium intercalated interstitially stabilized yttrium monochloride, LizYClZx (Z = H, C, O). in: SOLID STATE IONICS. 1993 ; Jahrgang 62, Nr. 3-4. S. 265-271.
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title = "Lithium ion mobility in lithium intercalated interstitially stabilized yttrium monochloride, LizYClZx (Z = H, C, O)",
abstract = "Regions of homogeneity were determined for the systems LizYClHx, LizYCLCx and LizYCLOx. Cell parameters for the different samples are given and trends, especially for the length of the c axis, are discussed. Temperature dependent Guinier-Simon investigations on different LizYClHx compounds show a shortening of the c axis at 480°C, which must be interpreted as a deintercalation of lithium. Y2Cl3 forms upon decomposition of LizYClHx at 1100°C. Conductivity measurements on a pellet of 7Li0.15YClD0.65 give a specific resistance of 2.2 × 10-1 ω·cm at 298 K which hints at electronic conductivity. Cell parameters, atomic positional parameters and occupation factors gained from a neutron powder diffraction experiment on 7Li0.15YClD0.65 are reported. The line shape of 7Li-NMR powder spectra is consistent with lithium at a definite lattice site. For all samples motional narrowing starts below room temperature. In the system LizYClC0.5 pronounced diffusion induced peaks of the spin-lattice relaxation rate T-11(T) of 7Li are observed above room temperature which exhibit the temperature dependence typical of disordered systems. In Li0.15YClD0.65 the 7Li spin-lattice relaxation rate, at the applied field of 4.7 T, does not show a significant peak but a continuous increase with temperature in the range from 150 K to 800 K.",
author = "Heiner Mattfeld and Gert Balzer-J{\"o}llenbeck and Gerd Meyer and Paul Heitjans",
note = "Funding Information: Financial support by the Deutsche Forschungs-gemeinschafBt,o nn (SFB 173 , TeilprojektA 17 ) and the Fond der Chemischen Industrie is greatfully acknowledged.",
year = "1993",
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doi = "10.1016/0167-2738(93)90381-C",
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issn = "0167-2738",
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TY - JOUR

T1 - Lithium ion mobility in lithium intercalated interstitially stabilized yttrium monochloride, LizYClZx (Z = H, C, O)

AU - Mattfeld, Heiner

AU - Balzer-Jöllenbeck, Gert

AU - Meyer, Gerd

AU - Heitjans, Paul

N1 - Funding Information: Financial support by the Deutsche Forschungs-gemeinschafBt,o nn (SFB 173 , TeilprojektA 17 ) and the Fond der Chemischen Industrie is greatfully acknowledged.

PY - 1993/8

Y1 - 1993/8

N2 - Regions of homogeneity were determined for the systems LizYClHx, LizYCLCx and LizYCLOx. Cell parameters for the different samples are given and trends, especially for the length of the c axis, are discussed. Temperature dependent Guinier-Simon investigations on different LizYClHx compounds show a shortening of the c axis at 480°C, which must be interpreted as a deintercalation of lithium. Y2Cl3 forms upon decomposition of LizYClHx at 1100°C. Conductivity measurements on a pellet of 7Li0.15YClD0.65 give a specific resistance of 2.2 × 10-1 ω·cm at 298 K which hints at electronic conductivity. Cell parameters, atomic positional parameters and occupation factors gained from a neutron powder diffraction experiment on 7Li0.15YClD0.65 are reported. The line shape of 7Li-NMR powder spectra is consistent with lithium at a definite lattice site. For all samples motional narrowing starts below room temperature. In the system LizYClC0.5 pronounced diffusion induced peaks of the spin-lattice relaxation rate T-11(T) of 7Li are observed above room temperature which exhibit the temperature dependence typical of disordered systems. In Li0.15YClD0.65 the 7Li spin-lattice relaxation rate, at the applied field of 4.7 T, does not show a significant peak but a continuous increase with temperature in the range from 150 K to 800 K.

AB - Regions of homogeneity were determined for the systems LizYClHx, LizYCLCx and LizYCLOx. Cell parameters for the different samples are given and trends, especially for the length of the c axis, are discussed. Temperature dependent Guinier-Simon investigations on different LizYClHx compounds show a shortening of the c axis at 480°C, which must be interpreted as a deintercalation of lithium. Y2Cl3 forms upon decomposition of LizYClHx at 1100°C. Conductivity measurements on a pellet of 7Li0.15YClD0.65 give a specific resistance of 2.2 × 10-1 ω·cm at 298 K which hints at electronic conductivity. Cell parameters, atomic positional parameters and occupation factors gained from a neutron powder diffraction experiment on 7Li0.15YClD0.65 are reported. The line shape of 7Li-NMR powder spectra is consistent with lithium at a definite lattice site. For all samples motional narrowing starts below room temperature. In the system LizYClC0.5 pronounced diffusion induced peaks of the spin-lattice relaxation rate T-11(T) of 7Li are observed above room temperature which exhibit the temperature dependence typical of disordered systems. In Li0.15YClD0.65 the 7Li spin-lattice relaxation rate, at the applied field of 4.7 T, does not show a significant peak but a continuous increase with temperature in the range from 150 K to 800 K.

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