Paramagnetic impurity effects in NMR determinations of hydrogen diffusion and electronic structure in metal hydrides. Gd3+ in YH2 and LaH2.25

T. -T. Phua, B. J. Beaudry, D. T. Peterson, D. R. Torgeson, R. G. Barnes, M. Belhoul, G. A. Styles, and E. F. W. Seymour
Phys. Rev. B 28, 6227 – Published 1 December 1983
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Abstract

Measurements are reported of the temperature dependence of the proton spin-lattice and spin-spin relaxation times T1 and T2 in yttrium and lanthanum dihydrides containing controlled levels of gadolinium as low as 50 ppm. The results demonstrate unambiguously that paramagnetic ions in concentrations so low as to have heretofore been regarded as insignificant have marked effects on the magnitude, frequency dependence, and temperature dependence of T1 and to a lesser extent on T2, and on the electronic structure and hydrogen diffusion parameters derived therefrom. The Gd3+ ion contributes an additional spin-lattice relaxation rate T1p, which in these hydrides arises entirely from the dipolar coupling between impurity and proton moments. Proton magnetization is transported to the relaxation centers by spin diffusion at low temperatures and by hydrogen-atom diffusion at intermediate and high temperatures. The rate R1p is directly proportional to Gd-ion concentration at both low and high temperatures, but in the atom diffusion regime R1p is 20-25 times greater than for spin diffusion. The impurity-induced relaxation is shown to have profound effects on the apparent nuclear-nuclear dipolar relaxation rate R1d associated with hydrogen diffusion. At impurity levels as low as 10 ppm Gd, a secondary minimum appears in the temperature dependence of T1 which may be readily misinterpreted in terms of a second motional process with lower activation energy. Even lower impurity levels yield a characteristic "slope-change" effect, which may be construed as indicating a change in the activation energy for hydrogen diffusion. At low temperatures R1p interferes with the determination of the conduction-electron contribution R1e and the Korringa product T1eT. Separation of R1e and R1p is complicated by the fact the R1p is not temperature independent as has typically been assumed. Methods of achieving this separation are discussed, and it is shown experimentally that this difficulty can be circumvented by replacing the major part of the hydrogen with deuterium, thereby inhibiting spin diffusion. Measurement of T1 as a function of resonance frequency and of T2 can also be of value in separating the various sources of relaxation.

  • Received 6 June 1983

DOI:https://doi.org/10.1103/PhysRevB.28.6227

©1983 American Physical Society

Authors & Affiliations

T. -T. Phua, B. J. Beaudry, D. T. Peterson, and D. R. Torgeson

  • Ames Laboratory—U.S. Department of Energy and Department of Physics, and Department of Materials Science and Engineering, Iowa State University, Ames, Iowa 50011

R. G. Barnes

  • Ames Laboratory—U.S. Department of Energy and Department of Physics, Iowa State University, Ames, Iowa 50011 and Laboratory of Atomic and Solid State Physics and Materials Science Center, Cornell University, Ithaca, New York 14850

M. Belhoul, G. A. Styles, and E. F. W. Seymour

  • Physics Department, University of Warwick, Coventry CV4 7AL, England

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Issue

Vol. 28, Iss. 11 — 1 December 1983

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