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Electronic structure of the Ni-Pd-P and Ni-Pt-P metallic glasses: A pulsed NMR study

Hines, W. A. and Glover, K. and Clark, W. G. and Kabacoff, L. T. and Modzelewski, C. U. and Hasegawa, R. and Duwez, P. (1980) Electronic structure of the Ni-Pd-P and Ni-Pt-P metallic glasses: A pulsed NMR study. Physical Review B, 21 (9). pp. 3771-3780. ISSN 0163-1829. doi:10.1103/PhysRevB.21.3771.

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A pulsed NMR and magnetic susceptibility study of the electronic structure is reported for the rapidly quenched metallic glass systems: (Ni0.50Pd0.50)100-xPx (where 16≦x≦26.5), (NiyPd1-y)80P20 (where 0.20≦y≦0.80), and (NiyPt1-y)75P25 (where 0.20≦y≦0.68). The 31P Knight shift and nuclear spin-lattice relaxation rate in all three systems depend only on the P concentration, x, and not the Ni concentration, y, nor whether the second transition metal is Pd or Pt. Both the shift and relaxation rate for 31P are attributed solely to the direct contact hyperfine interaction. The 195Pt Knight shift and magnetic susceptibility for (NiyPt1-y)75P25 do depend on both the Ni concentration and temperature, enabling a determination of the contributions to the shift arising from the direct contact hyperfine and core polarization interactions. The results are discussed in terms of a rigid two-band picture with estimates being made for the s- and d-band densities of states and hyperfine coupling constants. There is strong evidence for a transfer of charge from the P metalloid atoms (M) to the d states of the transition-metal atoms (T), which is consistent with the dense random packing model for T100-xMx metallic glasses.

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Additional Information:©1980 The American Physical Society Received 11 December 1979 One of us (W.A.H.) would like to express his deep appreciation to the Solid State Group, U.C.L.A., for the kind hospitality extended to him during his sabbatic leave visit. The pulsed NMR work at U.C.L.A. was supported by the NSF under Grant No. DMR 77-23577 and the UCLA Academic Senate Research Committee. The magnetic susceptibility work at the University of Connecticut was supported by both the AFOSR under Grant No. AFOSR 80-0030 and the University of Connecticut Research Foundation. Sample preparation and characterization at the California Institute of Technology was supported by the ERDA under Contract No. AT(04-3)-822.
Issue or Number:9
Record Number:CaltechAUTHORS:HINprb80
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Usage Policy:No commercial reproduction, distribution, display or performance rights in this work are provided.
ID Code:8541
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Deposited On:17 Aug 2007
Last Modified:08 Nov 2021 20:51

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