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 |
|