1991
DOI: 10.1103/physrevlett.66.477
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Isotope structure in optical spectra of LiYF_{4}:Ho^{3+}

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Cited by 82 publications
(39 citation statements)
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“…Their different zero-point motion might cause a site-random distortion of the crystal-field Hamiltonian, and isotope shifts in the optical transitions of dilute LiHo x Y 1−x F 4 have been reported. 37 We found that T c = 1.53± 0.03 in a crystal prepared exclusively with the 7 Li isotope, exactly the same as in natural Li samples. This result will be supplemented with a study of the critical field as a function of temperature.…”
Section: Discussionsupporting
confidence: 73%
“…Their different zero-point motion might cause a site-random distortion of the crystal-field Hamiltonian, and isotope shifts in the optical transitions of dilute LiHo x Y 1−x F 4 have been reported. 37 We found that T c = 1.53± 0.03 in a crystal prepared exclusively with the 7 Li isotope, exactly the same as in natural Li samples. This result will be supplemented with a study of the critical field as a function of temperature.…”
Section: Discussionsupporting
confidence: 73%
“…There is only one holmium isotope, 165 Ho, with nuclear spin I = 7/2. The free ion ground state, the 5 I 8 multiplet, is split by the tetragonal crystal field into 13 sublevels with a Γ 34 doublet ground state and the first excited Γ 2 singlet at 6.85 cm -1 higher energy (here Γ is the corresponding irreducible representation of the S 4 point symmetry group) [26,27]. The electronic and nuclear states are mixed mainly by the magnetic hyperfine interaction H hf =A (A = 0.795 GHz [26]).…”
Section: Methodsmentioning
confidence: 99%
“…In Fig. 3c the 9 K optical absorption spectrum for the Ho the interactions between the electronic dipole moment and the holmium nuclear moment has been exploited as a very sensitive tool to monitor the magnetic field at the nucleus and the RE electronic states coupling to the lattice [26,27]. The crystal field analysis previously described now includes in the Hamiltonian a contribution in the form V = A J J⋅I, where Ι is the nuclear total spin (for Ho 3+ I = 7/2); it should be remarked that such a contribution, without adding new free parameters in the fitting (the value of the hyperfine interaction constant A J can be found in [28]), accounts for most of the observed hyperfine split- tings.…”
mentioning
confidence: 99%