Unveiling the Atomic and Electronic Structure of Stacked-Cup Carbon Nanofibers

Abstract

We report results of comprehensive experimental exploration (X-ray photoemission, Raman and optical spectroscopy) of carbon nanofibers (CNFs) in combination with first-principles modeling. Core-level spectra demonstrate prevalence of sp2 hybridization of carbon atoms in CNF with a trace amount of carbon–oxygen bonds. The density functional theory (DFT)-based calculations demonstrated no visible difference between mono- and bilayers because σ-orbitals are related to in-plane covalent bonds. The influence of the distortions on π-peak is found to be significant only for bilayers as a result of π–π interlayer bonds formation. These results are supported by both experimental Raman and XPS valence band spectra. The combination of optical measurements with a theoretical modeling indicates the formation of optically active graphene quantum dots (GQDs) in the CNF matrix, with a radiative relaxation of the excited π* state. The calculated electronic structure of these GQDs is in quantitative agreement with the measured optical transitions and provides an explanation of the absence of visible contribution from these GQDs to the measured valence bands spectra.

Characterization of Carbon Nanostructures by Photoelectron Spectroscopies

“…In another study [281], the C 1s high-resolution core line revealed neglectable heteroatoms (O/C ratio is 0.019), confirming the purity of the sp 2 graphitic phases in the CNF. Optical measurements exhibit an absorption peak located in the UV region at 270 nm, while the emission spectra display a peak at 420 nm.…”