Atomic structure of plate-shaped nanodiamonds synthesized from chloroadamantane was identified with application of large-Qpowder diffraction data. Both reciprocal and real space methods of experimental data analysis were applied. Theoretical atomistic models of nanodiamonds were obtained with application of molecular dynamics (MD) simulations. It was found that examined nanodiamond samples with average grain size from 1.2 up to 2.5 nm are plates build from only six hexagonal carbon layers and they are terminated by (111)B surfaces with three dangling bonds. MD simulations showed that as a result of relaxation of surface stresses there appears a complex system of compressive and tensile strains across and parallel to the surface of the plate-nanodiamonds. Identification of the internal structure of nanodiamond was performed based on the analysis of differential interatomic distance diagrams derived from pair distribution functionsG(r). Based on MD simulations an atomic model of plate-grains of diamond was elaborated. Usefulness of lattice parameters determined in a routine diffraction data analysis for characterization of nanodiamonds is questioned. As an alternative the application of the apparent lattice parameter is recommended. A dependence of the overall apparent lattice parameter 〈alp〉 on the size and shape of nanodiamond grains terminated by low index crystal faces is presented.
Keywords: MD simulation; PDF analysis; high pressure synthesis; nanodiamond.
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