English
 
Help Privacy Policy Disclaimer
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT

Released

Journal Article

TbO+ in a calcium apatite matrix featuring a triple trigger-type relaxation of magnetization

MPS-Authors
/persons/resource/persons126838

Schnelle,  Walter
Walter Schnelle, Inorganic Chemistry, Max Planck Institute for Chemical Physics of Solids, Max Planck Society;

/persons/resource/persons126601

Felser,  Claudia
Claudia Felser, Inorganic Chemistry, Max Planck Institute for Chemical Physics of Solids, Max Planck Society;

/persons/resource/persons126670

Jansen,  Martin
Inorganic Chemistry, Max Planck Institute for Chemical Physics of Solids, Max Planck Society;

External Resource
No external resources are shared
Fulltext (restricted access)
There are currently no full texts shared for your IP range.
Fulltext (public)
There are no public fulltexts stored in PuRe
Supplementary Material (public)
There is no public supplementary material available
Citation

Kazin, P. E., Zykin, M. A., Magdysyuk, O. V., Utochnikova, V. V., Gorbachev, E. A., Kremer, R. K., et al. (2019). TbO+ in a calcium apatite matrix featuring a triple trigger-type relaxation of magnetization. Dalton Transactions, 48(16), 5299-5307. doi:10.1039/c9dt01120j.


Cite as: https://hdl.handle.net/21.11116/0000-0003-91D8-5
Abstract
Tb for Ca substituted hydroxyapatite ceramic samples with composition Ca10-xTbx(PO4)(6)(OH1-x/2-)(2), where x = 0.1, 0.5, were synthesized by solid-state reaction at 1300 degrees C in air, and their crystal structure, vibrational spectra, luminescence, and magnetic properties were studied. Implanting Tb3+ into the calcium apatite crystal lattice results in formation of an effective TbO+ ion which displays a short terbium-oxygen bond of 2.15 angstrom and a stretching vibration at 534 cm(-1). The Tb3+ electronic structure has been revealed by analyzing the luminescence spectra and dc/ac magnetization data. Accordingly, the ground state represents a pseudo doublet with M-J = +/- 6 and the first exited level is by 112 cm(-1) higher in energy. The ion exhibits field induced magnetic bistability with the magnetization reversing over the first exited state. Three paths of magnetization relaxation with field-temperature controlled switching between the paths have been identified.