17 research outputs found
Radiation-induced stable radicals in calcium phosphates: Results of multifrequency epr, ednmr, eseem, and endor studies
This article presents the results of a study of radiation-induced defects in various synthetic calcium phosphate (CP) powder materials (hydroxyapatite—HA and octacalcium phosphate—OCP) by electron paramagnetic resonance (EPR) spectroscopy at the X, Q, and W-bands (9, 34, 95 GHz for the microwave frequencies, respectively). Currently, CP materials are widely used in orthopedics and dentistry owing to their high biocompatibility and physico-chemical similarity with human hard tissue. It is shown that in addition to the classical EPR techniques, other experimental approaches such as ELDOR-detected NMR (EDNMR), electron spin echo envelope modulation (ESEEM), and electronnuclear double resonance (ENDOR) can be used to analyze the electron–nuclear interactions of CP powders. We demonstrated that the value and angular dependence of the quadrupole interaction for14 N nuclei of a nitrate radical can be determined by the EDNMR method at room temperature. The ESEEM technique has allowed for a rapid analysis of the nuclear environment and estimation of the structural positions of radiation-induced centers in various crystal matrices. ENDOR spectra can provide information about the distribution of the nitrate radicals in the OCP structure. © 2021 by the authors. Licensee MDPI, Basel, Switzerland. Published under the CC BY 4.0 license.Authors would like to thank the Russian Foundation for Basic Research, project no. 18-29-11086. Institute of Solid State Physics, University of Latvia as the Center of Excellence received funding from the European Union’s Horizon 2020 Framework Programme H2020-WIDESPREAD-01–2016-2017- TeamingPhase2 under grant agreement No. 739508, project CAMART2
HYSCORE Spectroscopy to Resolve Electron–Nuclear Structure of Vanadyl Porphyrins in Asphaltenes from the Athabasca Oil Sands In Situ Conditions
The purpose of this work is to analyze the electron–nuclear interactions of the vanadyl-porphyrin (VP) complexes in oil asphaltenes. Asphaltenes from the Athabasca oil sands were studied by HYperfine Sublevel CORrelation Spectroscopy (HYSCORE) electron paramagnetic resonance (EPR). It makes it possible to resolve and interpret complex hyperfine spectra of intrinsic VP with strong and weak hyperfine interactions between the electron magnetic moment and various nuclear spins (1H, 14N, 51V). The main parameters of spin-Hamiltonian for the VP spin system are determined. The axially symmetric structure of the VP complexes is revealed, and the local nuclear environment of the paramagnetic center is investigated. The results can be used for the study of asphaltene electron–nuclear structure and asphaltene aggregates with the aim of elucidating asphaltenes’ transformation(s) under the influence of external treatment
Incorporation of Manganese (II) in Beta-Tricalcium Phosphate from EPR and ENDOR Measurements for Powders
Powders of β-tricalcium phosphate (β-TCP, Ca3PO4) doped with manganese (Mn2+) are comprehensively analyzed with electron paramagnetic resonance (EPR) and electron-nuclear double resonance (ENDOR) techniques. The modeling of the spectra permitted to calculate the values of zero-field splitting (B20 = −904 MHz; B40 = −1.41 MHz and B43 = 195.2 MHz) and explain the origin of the low-field hyperfine structures as the allowed spin transitions of fine structure. Three structurally inequivalent positions for Mn2+ in the β-TCP crystal lattice are identified and their g-factors and hyperfine constants are quantified. The obtained results can serve as fundamental background to the study of structurally disordered matrices with high spin (S ≥ 1) impurities which are important for catalytic systems
Incorporation of Manganese (II) in Beta-Tricalcium Phosphate from EPR and ENDOR Measurements for Powders
Powders of β-tricalcium phosphate (β-TCP, Ca3PO4) doped with manganese (Mn2+) are comprehensively analyzed with electron paramagnetic resonance (EPR) and electron-nuclear double resonance (ENDOR) techniques. The modeling of the spectra permitted to calculate the values of zero-field splitting (B20 = −904 MHz; B40 = −1.41 MHz and B43 = 195.2 MHz) and explain the origin of the low-field hyperfine structures as the allowed spin transitions of fine structure. Three structurally inequivalent positions for Mn2+ in the β-TCP crystal lattice are identified and their g-factors and hyperfine constants are quantified. The obtained results can serve as fundamental background to the study of structurally disordered matrices with high spin (S ≥ 1) impurities which are important for catalytic systems
Study of Tricalcium Phosphate Ceramics Doped with Gadolinium Ions with Various EPR Techniques
Tricalcium phosphate (TCP)-based materials, such as β-Ca3(PO4)2 doped with rare earth ions (RE), have shown applications as biomaterials, lighting emitting materials, scintillating materials, in vivo imaging probes, and thermoluminescent dosimeters. Their properties are found to be dependent on the distribution of RE3+ on Ca2+ sites that can be controlled by pulsed electron paramagnetic resonance (EPR) and electron spin echo envelop modulation (ESEEM) experiments. The main spectroscopic parameters (spin Hamiltonian values) of Gd3+ and nitrogen impurity centers are quantitatively determined (g-factor, the fine structure parameters D and E, the hyperfine constants A) as well as dynamic characteristics: spin–lattice T1 and spin–spin T2 relaxation times. Based on the analysis of the EPR datasets, the interatomic distance between Gd3+ and 31P was estimated in the dipole–dipole approximation. Two structurally nonequivalent Gd3+ positions in the β-TCP structure have been identified. The obtained valuable results demonstrate applicability of modern EPR techniques to characterize Gd-TCP systems despite the powder structure of the material and high electron spin S = 7/2 of Gd3+ ions
Exploring the Properties of the V_B^- Defect in hBN: Optical Spin Polarization, Rabi Oscillations, and Coherent Nuclei Modulation
Optically active point defects in semiconductors have received great
attention in the field of solid-state quantum technologies. Hexagonal boron
nitride, with an ultra-wide band gap E_g = 6 eV, containing a negatively
charged boron vacancy (V_B^-) with unique spin, optical, and coherent
properties presents a new two-dimensional platform for the implementation of
quantum technologies. This work establishes the value of V_B^ - spin
polarization under optical pumping with {\lambda}ext = 532 nm laser using
high-frequency ({\nu}mw = 94 GHz) electron paramagnetic resonance (EPR)
spectroscopy. In optimal conditions polarization was found to be P = 38.4 %.
Our study reveals that Rabi oscillations induced on polarized spin states
persist for up to 30-40 microseconds, which is nearly two orders of magnitude
longer than what was previously reported. Analysis of the coherent
electron-nuclear interaction through the observed electron spin echo envelope
modulation (ESEEM) made it possible to detect signals from remote nitrogen and
boron nuclei, and to establish a corresponding quadrupole coupling constant Cq
= 180 kHz related to nuclear quadrupole moment of 14N. These results have
fundamental importance for understanding spin properties of boron vacancy
Polyvinylpyrrolidone—Alginate—Carbonate Hydroxyapatite Porous Composites for Dental Applications
An alternative approach for the currently used replacement therapy in dentistry is to apply materials that restore tooth tissue. Among them, composites, based on biopolymers with calcium phosphates, and cells can be applied. In the present work, a composite based on polyvinylpyrrolidone (PVP) and alginate (Alg) with carbonate hydroxyapatite (CHA) was prepared and characterized. The composite was investigated by X-ray diffraction, infrared spectroscopy, electron paramagnetic resonance (EPR) and scanning electron microscopy methods, and the microstructure, porosity, and swelling properties of the material were described. In vitro studies included the MTT test using mouse fibroblasts, and adhesion and survivability tests with human dental pulp stem cells (DPSC). The mineral component of the composite corresponded to CHA with an admixture of amorphous calcium phosphate. The presence of a bond between the polymer matrix and CHA particles was shown by EPR. The structure of the material was represented by micro- (30–190 μm) and nano-pores (average 8.71 ± 4.15 nm). The swelling measurements attested that CHA addition increased the polymer matrix hydrophilicity by 200%. In vitro studies demonstrated the biocompatibility of PVP-Alg-CHA (95 ± 5% cell viability), and DPSC located inside the pores. It was concluded that the PVP-Alg-CHA porous composite is promising for dentistry applications
Quantitative Analysis of Lewis Acid Centers of γ‑Alumina by Using EPR of the Adsorbed Anthraquinone as a Probe Molecule: Comparison with the Pyridine, Carbon Monoxide IR, and TPD of Ammonia
Quantitative
electron paramagnetic resonance (EPR) measurements
were done on the alumina oxide surface by using 9,10-anthraquinone
probe (AQ) with the AQ amount in the range of (0.5–20) wt %.
The nature of three paramagnetic centers observed simultaneously is
ascribed to the strong, medium, and weak Al Lewis acid sites on the
basis of combined EPR study/infrared (IR) spectroscopy of the adsorbed
CO and pyridine/temperature-programmed desorption (TPD) of ammonia.
It is shown how the optimal concentration of AQ probe molecule for
the exhaustive quantitative examination of alumina surface can be
determined directly from EPR. A possibility to characterize the surface
distribution of Lewis acid centers by AQ molecules is discussed