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Silicon nano- and microparticles obtained using electric-spark dispersion of silicon electrodes and granules in 40 wt% solution of methyl alcohol in water were investigated by ultrasoft X-ray emission spectroscopy, X-ray photoelectron spectroscopy, X-ray diffraction, scanning and transmission electron microscopies. In addition, the SiLα spectra of obtained silicon particles were modeled by superimposing the spectra of pure silicon and silicon oxide taken in certain weight ratios. It was found that the surfaces of Si nano- and microparticles obtained in 40 wt% solution of methyl alcohol in water are covered with silicon oxide and chemisorbents, while the core consists of crystalline silicon with a cubic face-centered lattice. The silicon nano- and microparticles show potential as an anode material to replace commonly used graphite electrodes. The charge capacity of the electrode based on mixture of Si nano- and microparticles with graphite powder was about 1272 mAh/g after ten cycles. [ABSTRACT FROM AUTHOR]

Hollow graphitic carbon nanoparticles (HGCNs) obtained by catalytic graphitization of acetylene carbon black (ACB) were investigated using ultra-soft X-ray emission spectroscopy. The electronic structures of the ACB HGCNs were compared with those of HGCNs obtained from iron carbide-filled carbon nanocapsules (Fe3C@CNCs) and Q-graphenes. The occupation of the π sub-band decreased in the following sequence: Fe3C@CNC HGCNs > ACB HGCNs > Q-graphenes. This sequence can be explained by changes in the occupations of the C2p states due to the formation of bonds between carbon and residual metal atoms within the HGCNs. It was also found that the contribution of the overlapping ofppπ+ppσ-states in the ACB HGCN walls toward the spectra of the HGNCs was greater in comparison with the reference Q-graphenes. It was established that ACB was not fully transformed into the HGCNs. Scanning and transmission electron microscopy methods were used to study the spatial structures and morphologies of the fabricated HGCNs. [ABSTRACT FROM PUBLISHER]

Investigations of the electronic structure of graphene nanosheets synthesized by the reduction of oxidized graphene nanosheets were carried out using ultra-soft X-ray emission spectroscopy (USXES). Oxidized graphene nanosheets were produced from carbon nanofiber starting material using a modified Hummers method. X-ray diffraction, and scanning and transmission electron microscopy investigations were used in addition to USXES to study the electronic structure evolution from carbon nanofibers to graphene nanosheets. The effect of the degree of corrugation of the graphene nanosheets on the fine structure of the CK(alpha)-emission bands was revealed by USXES. It was found that corrugation of the graphene nanosheets is caused by overlapping of the pi-orbitals and formation of mixed (sigma + pi)-states.