Superhyperfine interactions in Ce3+ doped LiYF4 crystal: ENDOR measurements

The first observation of the resolved Mims electron-nuclear double resonance (ENDOR) spectra from the nearby and remote nuclei of 19F and 7Li nuclei on impurity Ce3+ ions in LiYF4 crystal is reported. It shows that LiYF4:Ce3+ system can be exploited as a convenient matrix for performing spin manipulations and adjusting quantum computation protocols while ENDOR technique could be used for the investigation of electron-nuclear interaction with all the nuclei of the system and exploited for the electron-nuclear spin manipulations.Comment: 4 pages, 2 figures, 1 Table. Reported on Theor-2017 (Kazan, Russia) Conferenc

Spatial distribution of Nd3+ dopant ions in vitreous silica: A pulsed electron paramagnetic resonance spectroscopic study

The structural aspects of clustering of Nd3+ ions in Nd2O3-doped SiO2 glasses and the effect of Al3+ codoping on these clusters have been investigated with pulsed electron paramagnetic resonance (EPR) techniques over a temperature range of 1.5-4 K. The Nd2O3 concentrations in these glasses range between 700 and 2400 ppm by weight. The Nd3+ echo-detected EPR (EDEPR) spectra of the Al-free glasses show indications of weak exchange coupling between Nd3+ ions due to clustering. The EDEPR spectra also suggest that the local coordination environment of Nd3+ ions is affected by codoping with Al. The electronic spin-lattice relaxation rates are found to be not sensitive to the spatial distribution of Nd3+ ions over the entire temperature range of measurements. On the other hand, the concentration dependence of phase relaxation rates show clear evidence of clustering of Nd3+ ions in Al-free glasses, even at the lowest Nd2O3 doping levels. These Nd3+ clusters are found to break up and homogenize with an increase in the average Nd-Nd distance on codoping with Al. Analyses of the hyperfine sublevel correlation spectrum of a Nd and Al codoped glass indicate that the homogenization of Nd3+ clusters is possibly a consequence of the formation of Nd-O-Al linkages. © 2001 American Institute of Physics

Identification of Fe3+-Li+ complexes in ZnO by means of high-frequency EPR/ENDOR spectroscopy

Theoretical prediction of a high Curie temperature in ZnO doped with Mn, Fe, and other transition metals has stimulated the investigation of these materials by many research groups. Although charge-compensated Fe3+ centers in ZnO:Fe have been observed by means of EPR and have been known for decades, conclusions on the chemical nature of these defects are still contradictory. Originally, these centers were treated as Fe3+-Li + complexes with both ions occupying adjacent cationic sites. Recently, however, the centers were interpreted as a substitutional Fe 3+ ion with a vacancy at an adjacent zinc or oxygen site (Fe-V Zn or Fe-VO). In order to determine the chemical nature of the impurity associated with Fe3+, electron-nuclear double resonance (ENDOR) spectroscopy was used. ENDOR measurements reveal NMR transitions corresponding to nuclei with g-factor gN = 2.171 and spin I = 3/2. This unambiguously shows presence of Li as a charge compensator and also resolves contradictions with the theoretical prediction of the Fe-VO formation energy. The electric field gradients at the 7Li nuclei (within the Fe3+-Li+ complexes) were estimated to be significantly lower than the gradient at undistorted Zn sites. © 2013 Elsevier Inc. All rights reserved

High-frequency pulsed ENDOR spectroscopy of the NV- centre in the commercial HPHT diamond

© 2015 Elsevier Inc. All rights reserved. This work reports direct 94 GHz ENDOR spectroscopy of the 14N nuclei in the NV- centre in single-crystal diamond. Roadmaps of ENDOR frequencies were measured and hyperfine/quadrupole interaction parameters were obtained, with AX,Y = -2.7 MHz, AZ = -2.2 MHz and P = -4.8 MHz. The sign and value of each parameter was calculated using spin Hamiltonian matrix diagonalization, first and second order perturbation theory and confirmed experimentally. Magnetic field magnitude was measured by 13C ENDOR signal with 0.02% precision or 0.5 mT. The orientation of quadrupole, hyperfine and fine structure tensors are the same within error of experiment, g-factor is isotropic

Rural investment climate and business activities of agro-enterprise: Evidence from northern area of Vietnam

2013東京農業大

Application of Q-band electron spin echo spectrometer to investigation of glasses doped with rare earth ions

The Q-band electron spin echo (ESE) spectrometer which was created using modern microwave components is described. This simple incoherent apparatus was used with the X-band one for the study of phosphate and silicate glasses doped with non-Kramers rare earth Tb3+ ions. the EPR spectra measured by the ESE method have frequency independent peaks. The experimental results presumably show the existence of several types of paramagnetic centers in studied systems. © 1992 Springer

Spectroscopic study of the effect of N and F codoping on the spatial distribution of Er3+ dopant ions in vitreous SiO2

Pulsed electron paramagnetic resonance (EPR) spectroscopy has been used to study the influence of codoping with N and/or F on the clustering of Er 3+ ions in vitreous SiO2. Measurements of echo-detected EPR, spin-lattice and phase memory relaxation times, and electron spin-echo envelope modulation (ESEEM) were made in the X band. Er-N, Er-F, and Er-N-F codoped glasses show clear evidence of clustering of Er3+ ions at concentration levels ranging between 6.67 × 1018 cm -3 and 6.67 × 1019 cm-3. However, the relatively long phase memory relaxation time and the observability of ESEEM in the Er-N-F codoped glass strongly indicate that combined codoping with N and F is more effective in homogenization of the spatial distribution of Er 3+ ions in vitreous SiO2, although, the structural mechanism remains unclear. The ESEEM results provide evidence in favor of the presence of N in the vicinity of the Er3+ ions in Er-N-F codoped vitreous SiO2. © 2007 American Institute of Physics

Conventional electron paramagnetic resonance of Mn²⁺ in synthetic hydroxyapatite at different concentrations of the doped manganese

© 2018 Institute of Physics Publishing. All rights reserved. Powders of synthetic hydroxyapatite doped with Mn2+ ions in concentrations from 0.05 till 5 wt. % were investigated by conventional electron paramagnetic resonance (EPR). The parameters of the spin-Hamiltonian are derived. Partially resolved hyperfine structure in the magnetic fields corresponding to g ≈ 4.3 and g ≈ 9.4 is observed. The narrowing of the central peak with concentration is reported. A possibility to use the linewidth and intensity of the central peak for concentration measurements are discussed. The results could be used for the identification and qualification of Mn2+ in oil, mining and ore formations

ヨーロッパの総合医制度

Coherent spin dynamics of impurity Yb3+ ions in the CaWO4 single crystal has been studied using X - and W -band EPR. Rabi oscillations of the sample magnetization with damping times comparable to their period, driven by pulses of the microwave field with duration up to 5μs, were observed. The largest value of the single-qubit figure of merit (∼6400) is obtained for the high-field component in the Y 171 b X -band EPR spectrum. The spin-lattice relaxation time of the Yb3+ ions shortens with the increasing resonance frequency while the phase memory time, in contrast, grows noticeably. Variations of the phase memory times are interpreted in terms of spectral and instantaneous diffusions. The increase of the coherence time at the W band can be used for the application of rare-earth ions as qubits in quantum computing as it has been proposed recently. © 2009 The American Physical Society