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Individual nitrogen centers N0 and nitrogen pairs N 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. [ABSTRACT FROM AUTHOR]

We report on a nuclear magnetic resonance (NMR) study of ultrananocrystalline diamond (UNCD) materials produced by detonation technique. Analysis of the 13C and 1H NMR spectra, spin-spin and spin-lattice relaxation times in purified UNCD samples is presented. Our measurements show that UNCD particles consist of a diamond core that is partially covered by a sp 2-carbon fullerene-like shell. The uncovered part of outer diamond surface comprises a number of hydrocarbon groups that saturate the dangling bonds. Our findings are discussed along with recent calculations of the UNCD structure. Significant increase in the spin-lattice relaxation rate (in comparison with that of natural diamond), as well as stretched exponential character of the magnetization recovery, are attributed to the interaction of nuclear spins with paramagnetic centers which are likely fabrication-driven dangling bonds with unpaired electrons. We show that these centers are located mainly at the interface between the diamond core and shell. [ABSTRACT FROM AUTHOR]

We used X-ray diffraction, small-angle X-ray scattering, and scanning electron microscopy (SEM) to study the diamond graphite phase transition in detonation nanodiamond (ND) intercalated with Cu, Ni, Co and Fe for the first time. The study has been made before and after annealing in hydrogen and argon. The SEM data obtained support the idea of the hierarchic structure of ND with a size of primary cluster of about 5 nm. There are several levels of aggregation of primary clusters. We have shown that all the samples of ND are surface fractals. It means the structure can be characterized by three parameters: coherent scattering region (CSR), the size of scatterer A and fractal dimensionality D.The transition degree was identified by X-ray diffractometry from the peaks of bulk nanographite. Scanning electron microscopy was used to determine the sizes of metallic and carbon aggregates. We have found from the CRS, A and D data that the intercalation does not practically change the diamond core at annealing in hydrogen and its size is similar to that reported earlier. However the changes of the scatterer size and fractal dimensionality depend on type of intercalated metals in hydrogen annealing. [Copyright &y& Elsevier]

Porous silicon layers with introduced carbon-containing substances (fullerenes, ultradisperse diamond, carbohydrates) have been studied. It was found that high-temperature annealing of such layers in a hydrogen atmosphere leads to substantial transformation of the photoluminescence spectra. It is assumed that this results from the formation of cubic silicon carbide crystallites and the occurrence of the quantum-confinement effect in these crystallites. [ABSTRACT FROM AUTHOR]

Nanodiamond (ND) is one of the most attractive allotropic modification of carbon due to their unique physical and chemical properties. In the present review the current state of science and technology in the field of NDs is analyzed. ND can be used in various application and in different form e.g. as a dispersion phase in suspension, as a filler in composites, etc., so the sedimentation stability of ND in different media are under scrutiny. Thus, theoretical aspects of ND suspension coagulation mechanisms and the methods avoiding it were considered. The dependence of rheological behavior on particles modification was discussed as well. Various methods for the preparation and modification of NDs to obtain particles of various sizes on a nanometer scale with different physicochemical properties were reviewed. The area of practical application for NDs was considered on the example of polymer composites. The various manufacturing methods, mechanical properties and medical aspects for thermosetting, thermoplastic and elastomer ND composites were summarized., (Copyright © 2019. Published by Elsevier B.V.)

Ultrathin graphene films find their use as advantageous support for nano- and biomaterials investigations. Thin film causes a very slight deterioration to measured signals, thus providing more details of the object's structure at nanoscale. The ultimate thinness of graphene works in the best way for this purpose. However, obtaining suspended thin film of a large-area, which is convenient for applications, is often a relatively complicated and time-consuming task. Here we present a one-step 1-min technique for synthesis of an extremely thin (about 1-2 nm) continuous film suspended over cells of a conventional copper grid (50-400 μm mesh). This technique enables us to acquire a large-area film which is water-resistant, stable in organic solvents and can act as a support when studying nanoparticles or biomaterials. Moreover, the very mechanism of the film formation can be interesting from the point of view of other applications of ultrathin graphene oxide papers., (Copyright © 2014 Elsevier Ltd. All rights reserved.)

Intrinsic paramagnetic defects in ∼5 nm sized nanodiamonds, produced by various dynamic synthesis (DySND) techniques (detonation, shock-wave, pulsed laser ablation of solid carbon containing targets), have been studied by multi-frequency electron paramagnetic resonance (EPR). X-band (9-10 GHz) EPR spectra of DySND, in addition to the main intensive singlet Lorentzian-like EPR signal, reveal a low intensity doublet pattern within the half-field (HF) region (g ∼ 4). On transferring spectra to the Q-band (34 GHz) the shape of the HF pattern changes and splitting between doublet components is reduced from 10.4 to 2.6 mT. The HF patterns observed are attributed to the 'forbidden' ΔM(S) = 2 transitions between the Zeeman levels of some spin-triplet (S = 1) centers. The model of two triplet centers with g ∼ 2.003 and zero-field splitting parameters D(1) = 0.095 cm(-1) (TR1) and D(2) = 0.030 cm(-1) (TR2) satisfactorily describes experimental results at both microwave frequencies. The spin-triplet-type defects are observed in a wide variety of DySND samples irrespective of industrial supplier, cooling and carbon soot refinement methods, initial purity, disintegration, or subsequent targeted chemical modification. This indicates that the intrinsic defects with S = 1 in DySND systems are of universal origin.

We have developed a colloidal crystal templating method for preparation of diamond films with 2D and 3D ordered porous structures. The technological process involved breaks down into (a) impregnation into the pores of silica colloidal crystal (opal) films of detonation nanodiamond (DND) particles from their hydrosol; (b) microwave plasma-enhanced chemical vapor deposition (MWPECVD) regrowth with diamond of pores with high DND filling; (c) Ar(+) ion dry etching of fragments of shells of coalesced diamond crystallites which form in the course of MWPECVD on the surface of the SiO(2) beads making up the outer surface of a film and (d) wet etching of the SiO(2) template in aqueous HF solution. The final samples are either connected to the substrate or free-standing films of various thicknesses having 2D or 3D ordered porous structures. The morphology of the diamond films fabricated by this method replicates the pore network of the opal template. Raman measurements confirm the diamond structure of the synthesized ordered porous material.