Room Temperature High-Field Spin Dynamics of NV Defects in Sintered Diamonds

Sintered oriented nanodiamond arrays with the extremely high concentrations of the nitrogen-vacancy (NV) centers (up to 10³ ppm) were investigated by the W-band (94 GHz) electron spin echo electron paramagnetic resonance techniques. The NV centers were fabricated by the high-pressure high-temperature sintering of detonation nanodiamonds (DND) without the post or prior irradiation of the samples. The processes of polarization and recovery of the equilibrium population of the spin sublevels by optical and microwave pulses have been examined at room temperature in high magnetic fields corresponding to the fine-structure transitions for the NV defects at 94 GHz (3,250–3,450 mT). A long spin coherence time of 1.6 μs and spin–lattice relaxation time of 1.7 ms were measured. The results were compared with those obtained on the NV centers fabricated by the irradiation and subsequent annealing of the commercially available bulk diamonds. It was shown that the relaxation characteristics of the NV defects were similar in the both types of the samples despite the extremely high concentrations of NV defects and isolated nitrogen donors in the sintered DND.     

Electron paramagnetic resonance detection of the giant concentration of nitrogen vacancy defects in sintered detonation nanodiamonds

A giant concentration of nitrogen vacancy defects has been revealed by the electron paramagnetic resonance (EPR) method in a detonation nanodiamond sintered at high pressure and temperature. A high coherence of the electron spins at room temperature has been observed and the angular dependences of the EPR spectra indicate the complete orientation of the diamond system.     

Electron paramagnetic resonance in YbNiAl<Subscript>2</Subscript> single crystals with strong magnetic anisotropy

Anisotropy in the magnetic properties of YbNiAl₂ intermetallide has been studied. Electron paramagnetic resonance (EPR) signals assigned to the localized magnetic moments of trivalent ytterbium have been detected at temperatures below 20 K. Spin–lattice relaxation processes like the Orbach–Aminov process with participation of the first excited Stark sublevel of the Yb³⁺ ion with an energy of 96 K govern electron–spin dynamics and the disappearance of spectrum lines with a further increase in temperature. Strong magnetic anisotropy effects are discussed as a main reason for the appearance of electron paramagnetic resonance.     

Pb3+ radiation defects in Ca9Pb(PO4)6(OH)2 hydroxyapatite nanoparticles studied by high-field (W-band) EPR and ENDOR

W-band pulsed EPR and ENDOR investigations of X-ray irradiated nanoparticles of synthetic hydroxyapatite Ca(9)Pb(PO(4))(6)(OH)(2) are performed. It is shown that in the investigated species lead ions probably replace the Ca(1) position in the hydroxyapatite structure.     

Nitrogen-containing species in the structure of the synthesized nano-hydroxyapatite

Synthesized by the wet chemical precipitation technique, hydroxyapatite (HAp) powders with the sizes of the crystallites of 20–50 nm and 1 μm were analyzed by different analytical methods. By means of electron paramagnetic resonance (EPR) it is shown that during the synthesis process nitrate anions from the reagents (byproducts) could incorporate into the HAp structure. The relaxation times and EPR parameters of the stable axially symmetric NO ₃ ^2? paramagnetic centers detected after X-ray irradiation are measured with high accuracy. Analyses of high-frequency (95 GHz) electron-nuclear double resonance spectra from ¹H and ³¹P nuclei and ab initio density functional theory calculations allow suggesting that the paramagnetic centers and nitrate anions as the precursors of NO ₃ ^2? radicals preferably occupy PO ₄ ^3? site in the HAp structure.     

A study of hydroxyapatite nanocrystals by the multifrequency EPR and ENDOR spectroscopy methods

Specimens of powders of hydroxyapatite (Ca₁₀(PO₄)₆(OH)₂) with average crystallite sizes in the range of 20–50 nm synthesized by the wet precipitation method have been investigated by the multifrequency (9 and 94 GHz) electron paramagnetic resonance (EPR) and electron-nuclear double resonance (ENDOR) methods. In specimens subjected to X-ray irradiation at room temperature, EPR signals that are caused by nitrogen compounds have been observed. Numerical calculations performed in terms of the density functional theory show that the observed EPR signal is caused by the occurrence of paramagnetic centers, the structure of which is NO ₃ ^2? and which replace the positions of PO ₄ ^3? in the hydroxyapatite structure.     

Defects in Nanodiamonds: Application of High-Frequency cw and Pulse EPR,ODMR

Different aspects of applications of electron paramagnetic resonance (EPR) based techniques including high frequency (HF) electron spin echo (ESE), electron-nuclear double resonance (ENDOR) and optically detected magnetic resonance (ODMR) approaches to study diamond nanostructures are examined.