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Local structure and electronic-charge distribution at the rare-earth site of compounds (Gd[sub 1[minus][ital x]R[ital x]])[sub 2]CuO[sub 4], [ital R]=Pr, Nd, Sm, and Eu

Journal Article · · Physical Review, B: Condensed Matter; (United States)
; ;  [1]
  1. Kernforschungszentrum Karlsruhe, Institut fuer Nukleare Festkoerperphysik, P.O. Box 3640, W-7500 Karlsruhe (Germany)

Mixed compounds (Gd[sub 1[minus][ital x]R[ital x]])[sub 2]CuO[sub 4], [ital R]=Pr, Nd, Sm, and Eu, with [ital T][prime] structure, were studied by x-ray diffraction and by [sup 155]Gd Moessbauer spectroscopy. Structural parameters (unit cell volume, [ital c]/3[ital a]) differ considerably for compounds with different rare earths. In contrast, the variation of the isomer shift [delta][sub [ital I][ital S]] and of the electric-field gradient [ital V][sub [ital z][ital z]] at [sup 155]Gd nuclei with Gd concentration is practically identical in the systems with Pr, Nd, and Sm. These results demonstrate that [delta][sub [ital I][ital S]] and [ital V][sub [ital z][ital z]] in the compounds [ital R][sub 2]CuO[sub 4] are primarily determined by contributions of the local electronic-charge distribution at the rare-earth site, which depends weakly upon the positions of the ions as determined by the structural parameters. Furthermore, our results indicate the possibility of an influence of the degree of covalency upon the transition temperature [ital T][sub [ital c]] achieved in Ce-doped compounds.

OSTI ID:
5528536
Journal Information:
Physical Review, B: Condensed Matter; (United States), Journal Name: Physical Review, B: Condensed Matter; (United States) Vol. 48:1; ISSN PRBMDO; ISSN 0163-1829
Country of Publication:
United States
Language:
English

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