Large magnetoresistance in non-magnetic silver chalcogenides

R. Xu, A. Husmann, T. F. Rosenbaum (), M.-L. Saboungi, J. E. Enderby and P. B. Littlewood
Additional contact information
R. Xu: The University of Chicago
A. Husmann: The University of Chicago
T. F. Rosenbaum: The University of Chicago
M.-L. Saboungi: Argonne National Laboratory
J. E. Enderby: Argonne National Laboratory
P. B. Littlewood: Bell Laboratories, Lucent Technologies

Nature, 1997, vol. 390, issue 6655, 57-60

Abstract: Abstract Several materials have been identified over the past few years as promising candidates for the development of new generations of magnetoresistive devices. These range from artificially engineered magnetic multilayers1 and granular alloys2,3, in which the magnetic-field response of interfacial spins modulates electron transport to give rise to ‘giant’ magnetoresistance4, to the manganite perovskites5,6,7, in which metal–insulator transitions driven by a magnetic field give rise to a ‘colossal’ magnetoresistive response (albeit at very high fields). Here we describe a hitherto unexplored class of magnetoresistive compounds, the silver chalcogenides. At high temperatures, the compounds Ag2S, Ag2Se and Ag2Te are superionic conductors; below ∼400 K, ion migration is effectively frozen and the compounds are non-magnetic semiconductors8,9 that exhibit no appreciable magnetoresistance10. We show that slightly altering the stoichiometry can lead to a marked increase in the magnetic response. At room temperature and in a magnetic field of ∼55 kOe, Ag2+δSe and Ag2+δTe show resistance increases of up to 200%, which are comparable with the colossal-magnetoresistance materials. Moreover, the resistance of our most responsive samples exhibits an unusual linear dependence on magnetic field, indicating both a potentially useful response down to fields of practical importance and a peculiarly long length scale associated with the underlying mechanism.

Date: 1997
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DOI: 10.1038/36306

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