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Title:
Compression of klockmannite, CuSe
Authors:
Peiris, Suhithi M.; Pearson, Tania T.; Heinz, Dion L.
Affiliation:
AA(Department of Chemistry, University of Chicago, Chicago, Illinois 60637), AB(Department of Chemistry, University of Michigan, Ann Arbor, Michigan 48109), AC(Department of Geophysical Sciences and James Franck Institute, University of Chicago, Chicago, Illinois 60637)
Publication:
Journal of Chemical Physics, Volume 109, Issue 2, pp. 634-636 (1998). (JChPh Homepage)
Publication Date:
07/1998
Origin:
AIP
PACS Keywords:
High-pressure and shock wave effects in solids and liquids, Solid-solid transitions, Other nonmetallic inorganics, Disordered solids, Equations of state of specific substances, Crystal binding; cohesive energy, Deformation and plasticity, Deformation, plasticity, and creep
Abstract Copyright:
(c) 1998: American Institute of Physics.
DOI:
10.1063/1.476601
Bibliographic Code:
1998JChPh.109..634P

Abstract

Copper selenide (CuSe) was compressed in a diamond anvil cell at room temperature up to a pressure of 52 GPa and studied using energy dispersive x-ray diffraction and Raman spectroscopy. CuSe is nearly isostructural with copper sulfide (CuS), and a previous study indicates that copper sulfide undergoes reversible pressure-induced amorphization at 18 GPa. The intensity of the x-ray diffraction peaks for CuSe decrease slowly, however, they never completely disappear up to a pressure of 52 GPa. The third-order Birch-Murnaghan equation of state fit to the data yields K0=96.9+/-5.3 GPa and K0'=4.1+/-0.5. Vinet's universal equation of state yields essentially identical parameters. Raman spectroscopy demonstrates that upon compression, the S-S bond in CuS compresses differently than the Se-Se bond in CuSe, possibly accounting for the different high pressure behavior of these two very similar compounds.
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