Electron spin resonance detection and identification of nitrogen centers in nanodiamonds

Individual nitrogen centers N0 and nitrogen pairs N 2 + have been detected and identified in natural diamond nanocrystals by means of the high-frequency electron spin resonance method. The N0 nitrogen centers have been observed in synthetic diamond nanocrystallites with a size of less than 10 nm produced by high-temperature high-pressure sintering of detonation nanodiamonds. Thus, the possibility of the stable state of impurity nitrogen atoms in diamond nanoparticles has been demonstrated. © 2009 Pleiades Publishing, Ltd

Nitrogen centers in nanodiamonds: EPR studies

Electron paramagnetic resonance (EPR) and electron spin echo (ESE) at X-band (9.4 GHz) and W-band (94 GHz) have been used to study defects in natural diamond nanocrystals, detonation nanodiamond (ND) with a size of ∼ 4.5 nm and detonation ND after high-pressure hightemperature (HTHP) sintering with a size of ∼ 8.5 nm. Based on identification of atomic nitrogen centers N0 and nitrogen pairs N2 + detected by means of the high frequency EPR and ESE in natural diamond nanocrystals, atomic nitrogen centers N0 have been discovered in nanodiamond core in detonation ND and detonation ND after sintering. In addition EPR signal of multi-vacancy centers with spin 3/2 seems to be observed in diamond core of detonation ND. © (2010) Trans Tech Publications

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. © 2013 Springer-Verlag Wien

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. © 2010 Pleiades Publishing, Ltd

Detection and identification of nitrogen centers in nanodiamond: EPR studies

Electron paramagnetic resonance (EPR) and electron spin echo (ESE) at X-band and at high-frequency W-band (95 GHz) have been used to study natural diamond nanocrystals, detonation nanodiamond (ND) with a size of ∼ 4.5 nm and detonation ND after high-temperature, high-pressure sintering with a size of ∼ 8.5 nm. Isolated nitrogen centers N 0 and nitrogen pairs N2+ have been detected and identified, and their structure has been unambiguously determined by means of the high frequency EPR and ESE in natural diamond nanocrystals. In detonation ND and detonation ND after sintering, isolated nitrogen centers N 0 have been discovered in nanodiamond core. In addition EPR signals of multivacancy centers with spin 3/2 seem to be observed in nanodiamond core of detonation ND. Copyright © Taylor & Francis Group, LLC