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dc.contributor.author | Hirvonen M. | |
dc.contributor.author | Katila T. | |
dc.contributor.author | Riski K. | |
dc.contributor.author | Teplov M. | |
dc.contributor.author | Malkin B. | |
dc.contributor.author | Phillips N. | |
dc.contributor.author | Wun M. | |
dc.date.accessioned | 2018-09-14T20:47:53Z | |
dc.date.available | 2018-09-14T20:47:53Z | |
dc.date.issued | 1975 | |
dc.identifier.issn | 0163-1829 | |
dc.identifier.uri | https://dspace.kpfu.ru/xmlui/handle/net/132731 | |
dc.description.abstract | The magnetic properties of terbium ethyl sulphate, a singlet crystal-field ground-state system with predominantly dipolar interactions between the magnetic ions, have been studied theoretically and experimentally at low temperatures. The susceptibilities parallel and perpendicular to the hexagonal c axis were measured in the temperature range 0.03-4 K by a superconducting-quantum-interference-device magnetometer in connection with a dilution refrigerator. In addition, the heat capacity of a powdered sample was measured. The results indicate a cooperative transition at 0.24 K. The data give indirect information on the value of the crystal-field splitting, which has not been measured before. The behavior of the longitudinal susceptibility is consistent with a picture of a ferromagnetic transition into long and thin domains along the c axis. The much smaller transverse susceptibility shows an unexpected abrupt change at 0.24 K. Theoretical calculations on the magnetic properties are presented. The molecular-field approximation, two- and three-particle "cluster" models and high-temperature expansion are considered in turn. The predictions of the three-particle cluster model are closest to the experimental data. © 1975 The American Physical Society. | |
dc.relation.ispartofseries | Physical Review B | |
dc.title | Magnetic ordering in terbium ethyl sulphate | |
dc.type | Article | |
dc.relation.ispartofseries-issue | 11 | |
dc.relation.ispartofseries-volume | 11 | |
dc.collection | Публикации сотрудников КФУ | |
dc.relation.startpage | 4652 | |
dc.source.id | SCOPUS01631829-1975-11-11-SID34447538834 |