Compression of klockmannite, CuSe
dc.contributor.author | Peiris, Suhithi M. | en_US |
dc.contributor.author | Pearson, Tania T. | en_US |
dc.contributor.author | Heinz, Dion L. | en_US |
dc.date.accessioned | 2010-05-06T22:51:04Z | |
dc.date.available | 2010-05-06T22:51:04Z | |
dc.date.issued | 1998-07-08 | en_US |
dc.identifier.citation | Peiris, Suhithi M.; Pearson, Tania T.; Heinz, Dion L. (1998). "Compression of klockmannite, CuSe." The Journal of Chemical Physics 109(2): 634-636. <http://hdl.handle.net/2027.42/70875> | en_US |
dc.identifier.uri | https://hdl.handle.net/2027.42/70875 | |
dc.description.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 GPaK0=96.9±5.3GPa and K0′ = 4.1±0.5.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. © 1998 American Institute of Physics. | en_US |
dc.format.extent | 3102 bytes | |
dc.format.extent | 80184 bytes | |
dc.format.mimetype | text/plain | |
dc.format.mimetype | application/pdf | |
dc.publisher | The American Institute of Physics | en_US |
dc.rights | © The American Institute of Physics | en_US |
dc.title | Compression of klockmannite, CuSe | en_US |
dc.type | Article | en_US |
dc.subject.hlbsecondlevel | Physics | en_US |
dc.subject.hlbtoplevel | Science | en_US |
dc.description.peerreviewed | Peer Reviewed | en_US |
dc.contributor.affiliationum | Department of Chemistry, University of Michigan, Ann Arbor, Michigan 48109 | en_US |
dc.contributor.affiliationother | Department of Chemistry, University of Chicago, Chicago, Illinois 60637 | en_US |
dc.contributor.affiliationother | Department of Geophysical Sciences and James Franck Institute, University of Chicago, Chicago, Illinois 60637 | en_US |
dc.description.bitstreamurl | http://deepblue.lib.umich.edu/bitstream/2027.42/70875/2/JCPSA6-109-2-634-1.pdf | |
dc.identifier.doi | 10.1063/1.476601 | en_US |
dc.identifier.source | The Journal of Chemical Physics | en_US |
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dc.owningcollname | Physics, Department of |
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