Vibrational and electronic structures of tin selenide nanowires confined inside carbon nanotubes.

We study vibrational and electronic properties of tin selenide (SnSe) nanowires encapsulated in single walled carbon nanotubes (SWCNT) by combining experimental Raman spectroscopy and density functional theory (DFT) calculations at the Heyd-Scuseria-Ernzerhof (HSE) level. The theoretically investigated standalone SnSe nanowires are Sn 4 Se 4 with square (2 × 2) atomic arrangement and Sn 6 Se 6 with a repeating hexagonal Mo 6 S 6 -like structure. Raman data support the theoretical prediction that the square (2 × 2) nanowires possess specific modes at 151 and 185 cm−1, whereas the hexagonal Sn 6 Se 6 structure is characterized by a mode appearing at ~ 235 cm−1. Calculations predict that the (2 × 2) nanowire has an electronic gap of 1.5 eV and the Sn 6 Se 6 nanowire presents a semi-metallic character. Raman spectra of composite SnSe@SWCNT samples show that the radial breathing mode of the nanotubes is strongly suppressed indicating interaction between SWCNT and the encapsulated SnSe nanowire while the Fano asymmetry parameter of the G band is increased. [Display omitted] • Raman spectra of extreme SnSe 1D crystals embedded in carbon nanotubes. • First use of HSE functional for predicting phonons and band structures in these nanowires. • Presence of encapsulated SnSe modifies the vibrational and electronic properties of the nanotube walls. • SnSe 1D embedded crystals disclose drastic changes in electronic properties with respect to the bulk phase. [ABSTRACT FROM AUTHOR]