Diffusion processes in solid Li-Mg and Li-Ag alloys and the spin-lattice relaxation of 8Li

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Autoren

  • A. Korblein
  • P. Heitjans
  • H.-J. Stockmann
  • F. Fujara
  • H. Ackermann
  • W. Buttler
  • K. Dorr
  • H. Grupp

Externe Organisationen

  • Philipps-Universität Marburg
Forschungs-netzwerk anzeigen

Details

OriginalspracheEnglisch
Aufsatznummer011
Seiten (von - bis)561-577
Seitenumfang17
FachzeitschriftJournal of Physics F: Metal Physics
Jahrgang15
Ausgabenummer3
PublikationsstatusVeröffentlicht - 1985
Extern publiziertJa

Abstract

The spin-lattice relaxation (SLR) of polarised radioactive 8Li nuclei in solid Li-based alloys containing 2-11 at.% Mg and 1.6-10 at.% Ag was measured via their asymmetric beta -decay radiation. For temperatures T<200K SLR is due to conduction electrons only, and the Korringa relation is found to hold in the concentration range covered. For T=200-450K, SLR is additionally influenced by atomic diffusion. The diffusional contribution consists of a dipolar part as in pure Li and a quadrupolar part induced by the solute ions. The analysis is based on the concept of two-exponential SLR for spin I=2. In Li-Mg the self-diffusion of Li and the diffusion of the solute ions are found to be slowed down on alloying. The ratio of the jump rates of Li and Mg appears to be determined simply by their atomic masses. In the case of the dilute alloy Li-1.6 at.% Ag, which is amenable to theoretical diffusion models, comparison with tracer results favours an interstitial-vacancy pair mechanism. In the framework of this model Ag is found to diffuse faster than Li.

ASJC Scopus Sachgebiete

Zitieren

Diffusion processes in solid Li-Mg and Li-Ag alloys and the spin-lattice relaxation of 8Li. / Korblein, A.; Heitjans, P.; Stockmann, H.-J. et al.
in: Journal of Physics F: Metal Physics, Jahrgang 15, Nr. 3, 011, 1985, S. 561-577.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Korblein, A, Heitjans, P, Stockmann, H-J, Fujara, F, Ackermann, H, Buttler, W, Dorr, K & Grupp, H 1985, 'Diffusion processes in solid Li-Mg and Li-Ag alloys and the spin-lattice relaxation of 8Li', Journal of Physics F: Metal Physics, Jg. 15, Nr. 3, 011, S. 561-577. https://doi.org/10.1088/0305-4608/15/3/011
Korblein, A., Heitjans, P., Stockmann, H.-J., Fujara, F., Ackermann, H., Buttler, W., Dorr, K., & Grupp, H. (1985). Diffusion processes in solid Li-Mg and Li-Ag alloys and the spin-lattice relaxation of 8Li. Journal of Physics F: Metal Physics, 15(3), 561-577. Artikel 011. https://doi.org/10.1088/0305-4608/15/3/011
Korblein A, Heitjans P, Stockmann HJ, Fujara F, Ackermann H, Buttler W et al. Diffusion processes in solid Li-Mg and Li-Ag alloys and the spin-lattice relaxation of 8Li. Journal of Physics F: Metal Physics. 1985;15(3):561-577. 011. doi: 10.1088/0305-4608/15/3/011
Korblein, A. ; Heitjans, P. ; Stockmann, H.-J. et al. / Diffusion processes in solid Li-Mg and Li-Ag alloys and the spin-lattice relaxation of 8Li. in: Journal of Physics F: Metal Physics. 1985 ; Jahrgang 15, Nr. 3. S. 561-577.
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abstract = "The spin-lattice relaxation (SLR) of polarised radioactive 8Li nuclei in solid Li-based alloys containing 2-11 at.% Mg and 1.6-10 at.% Ag was measured via their asymmetric beta -decay radiation. For temperatures T<200K SLR is due to conduction electrons only, and the Korringa relation is found to hold in the concentration range covered. For T=200-450K, SLR is additionally influenced by atomic diffusion. The diffusional contribution consists of a dipolar part as in pure Li and a quadrupolar part induced by the solute ions. The analysis is based on the concept of two-exponential SLR for spin I=2. In Li-Mg the self-diffusion of Li and the diffusion of the solute ions are found to be slowed down on alloying. The ratio of the jump rates of Li and Mg appears to be determined simply by their atomic masses. In the case of the dilute alloy Li-1.6 at.% Ag, which is amenable to theoretical diffusion models, comparison with tracer results favours an interstitial-vacancy pair mechanism. In the framework of this model Ag is found to diffuse faster than Li.",
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Download

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T1 - Diffusion processes in solid Li-Mg and Li-Ag alloys and the spin-lattice relaxation of 8Li

AU - Korblein, A.

AU - Heitjans, P.

AU - Stockmann, H.-J.

AU - Fujara, F.

AU - Ackermann, H.

AU - Buttler, W.

AU - Dorr, K.

AU - Grupp, H.

PY - 1985

Y1 - 1985

N2 - The spin-lattice relaxation (SLR) of polarised radioactive 8Li nuclei in solid Li-based alloys containing 2-11 at.% Mg and 1.6-10 at.% Ag was measured via their asymmetric beta -decay radiation. For temperatures T<200K SLR is due to conduction electrons only, and the Korringa relation is found to hold in the concentration range covered. For T=200-450K, SLR is additionally influenced by atomic diffusion. The diffusional contribution consists of a dipolar part as in pure Li and a quadrupolar part induced by the solute ions. The analysis is based on the concept of two-exponential SLR for spin I=2. In Li-Mg the self-diffusion of Li and the diffusion of the solute ions are found to be slowed down on alloying. The ratio of the jump rates of Li and Mg appears to be determined simply by their atomic masses. In the case of the dilute alloy Li-1.6 at.% Ag, which is amenable to theoretical diffusion models, comparison with tracer results favours an interstitial-vacancy pair mechanism. In the framework of this model Ag is found to diffuse faster than Li.

AB - The spin-lattice relaxation (SLR) of polarised radioactive 8Li nuclei in solid Li-based alloys containing 2-11 at.% Mg and 1.6-10 at.% Ag was measured via their asymmetric beta -decay radiation. For temperatures T<200K SLR is due to conduction electrons only, and the Korringa relation is found to hold in the concentration range covered. For T=200-450K, SLR is additionally influenced by atomic diffusion. The diffusional contribution consists of a dipolar part as in pure Li and a quadrupolar part induced by the solute ions. The analysis is based on the concept of two-exponential SLR for spin I=2. In Li-Mg the self-diffusion of Li and the diffusion of the solute ions are found to be slowed down on alloying. The ratio of the jump rates of Li and Mg appears to be determined simply by their atomic masses. In the case of the dilute alloy Li-1.6 at.% Ag, which is amenable to theoretical diffusion models, comparison with tracer results favours an interstitial-vacancy pair mechanism. In the framework of this model Ag is found to diffuse faster than Li.

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