This article presents the results of experiments in which the 19 429.67-${\mathrm{cm}}^{\mathrm{\ensuremath{-}}1}$ emission of an
Ar+ laser is used to pump the
Z1,
4I9/2, \ensuremath{\mu}=(5/2\ensuremath{\rightarrow}
F1,
2G9/2, \ensuremath{\mu}=(1/2 transition of
Nd3+ ions dilutely substituted at
La3+ sites in
LaCl3 crystals in an \ensuremath{\sim}1.6-K bath of liquid He. In some of the work
Er3+ ions are also present. When an external magnetic field is applied electron paramagnetic resonance (EPR) absorption of microwave energy by either
Nd3+ or
Er3+ results in marked intensity changes of
Nd3+ fluorescence emissions. The essential new feature of this work is the observation of the importance of the effects of the heating of the crystal above the bath temperature by both optical and microwave absorption. The heating by phonons generated in the radiationless transitions associated with the optical pumping cycle results in the emission of 17 E and D
Nd3+ fluorescences not observed in previous work with the crystal at \ensuremath{\sim}1.6 K. Because of the encapsulation of the crystals in silica envelopes in these experiments, the heating effects are especially marked at higher laser powers.These new fluorescences result from the state population redistributions effected by the rise in temperature of the crystal. EPR microwave absorption by either
Nd3+ or
Er3+ accompanied by spin-lattice relaxation results in a further increase in crystal temperature and further
Nd3+ state population redistributions with concommitant changes in the intensities of the fluorescence emissions from these states of
Nd3+. This affords a new mechanism for optically detected magnetic resonance (ODMR) of these rare-earth ions. This new mechanism for ODMR produces optical signals strikingly different from those previously studied which result from the changes in the populations of the two components of the ground
Z1 doublet of
Nd3+ produced by
Z1 microwave absorption or by microwave absorption by the
Er3+ ground doublet with subsequent transfer of Zeeman quanta between
Er3+ and
Nd3+ and resultant changes in optical pumping rates and fluorescence emissions. The factors contributing to the new mechanism for ODMR also account for the observed changes with temperature in the characters of the decays of the ODMR signals when microwave irradiation is terminated. With constant intensity laser irradiation in the absence of external magnetic fields the 28 observed fluorescence emissions oscillate in synchrony at frequencies (1/2 to (1/3 Hz, when the laser irradiation intensity lies in a certain narrow range. Several mechanisms considered as explanations of this phenomenon have failed to account for its observed features. It is clear, however, that these oscillations of emission intensity are accompanied by oscillations in the temperature of the crystal and of the populations of the emitting states.
We report on optical detection of a single photostable Ce(3+) ion in an yttrium aluminium garnet (YAG) crystal and on its magneto-optical properties at room temperature. The spin quantum state of the emitting level of a single cerium ion in YAG can be initialized by a circularly polarized laser pulse. Coherent precession of the electron spin is read out by observing temporal behavior of circularly polarized fluorescence of the ion. This implies direct mapping of the spin quantum state of Ce(3+) ion onto the polarization state of the emitted photon and represents the quantum interface between a single spin and a single photon.
The spin relaxation dynamics of
Ce3+ ions in heavily cerium-doped YAG crystals is studied using pulse-electron paramagnetic resonance and time-resolved pump-probe Faraday rotation. Both techniques address the
4f ground state, while pump-probe Faraday rotation also provides access to the excited
5d state. We measure a millisecond spin-lattice relaxation time
T1, a microsecond spin coherence time
T2, and a $\ensuremath{\sim}10$ ns inhomogeneous spin dephasing time
T2∗ for the
Ce3+ ground state at low temperatures. The spin-lattice relaxation of
Ce3+ ions is due to modified Raman processes involving the optical phonon mode at $\ensuremath{\sim}\phantom{\rule{0.16em}{0ex}}125\phantom{\rule{0.16em}{0ex}}{\mathrm{cm}}^{\ensuremath{-}1}$. The relaxation at higher temperature goes through a first excited level of the
2F25 term at about $\ensuremath{\hbar}\ensuremath{\omega}\ensuremath{\approx}228\phantom{\rule{4pt}{0ex}}{\mathrm{cm}}^{\ensuremath{-}1}$. Effects provided by the hyperfine interaction of the
Ce3+ with the
27Al nuclei are observed.
The frequency-field and orientation dependences of the electron paramagnetic resonance (EPR) spectra are measured for impurity Tm 3+ ions in yttrium orthosilicate (Y 2 SiO 5 ) single crystals by stationary EPR spectroscopy in the frequency range of 50–100 GHz at 4.2 K. The position of the impurity ion in the crystal lattice and its magnetic characteristics are determined. The temperature dependences of the spin–lattice and phase relaxation times are measured by pulse EPR methods in the temperature range of 5–15 K and the high efficiency of the direct single-phonon mechanism of spin–lattice relaxation is established. This greatly shortens the spin–lattice relaxation time at low temperatures and makes impurity Tm 3+ ions in Y 2 SiO 5 a promising basis for the implementation of high-speed quantum memory based on rare-earth ions in dielectric crystals.
Electron paramagnetic resonance (EPR) spectroscopy of rare earth ions in crystals is a powerful tool to analyze the hyperfine structure of the rare earth ground state. This can be useful for coherent spectroscopy and quantum information applications where the hyperfine structure of the electronic levels is used. In this work, we give a detailed analysis of the hyperfine structure of the ground state
[4I15∕2(0)] of
Er3+ ions in
Y2SiO5. The electronic Zeeman, hyperfine, and quadrupole matrices are obtained from angular variations of the magnetic field in three orthogonal crystal planes. An excellent agreement is obtained between experimental and simulated magnetic field positions and relative intensities of EPR lines.
We report on a high-resolution optical and magneto-optical spectroscopy, luminescence, and electron paramagnetic resonance (EPR) studies of yttrium orthophosphate single crystals doped with erbium, which are promising telecom-wavelength materials for applications in quantum electronics and quantum information processing. An observation of the hyperfine structure in optical spectra of
167Er isotope in
Er:YPO4 is presented. Energies and symmetries of 40 crystal-field levels of
Er3+ in
Er:YPO4 and
g factors of some of them were determined and successfully modeled on the basis of crystal-field calculations. The obtained set of crystal-field parameters was used in modeling the hyperfine structure observed in the optical and EPR spectra of
Er:YPO4 single crystals.