Bandgap Shrinkage and Charge Transfer in 2D Layered SnS2 Doped with V for Photocatalytic Efficiency Improvement

Effects of electronic and atomic structures of V-doped 2D layered SnS2 are studied using X-ray spectroscopy for the development of photocatalytic/photovoltaic applications. Extended X-ray absorption fine structure measurements at V K-edge reveal the presence of V-O and V-S bonds which form the intercalation of tetrahedral O-V-S sites in the van der Waals (vdW) gap of SnS2 layers. X-ray absorption near-edge structure (XANES) reveals not only valence state of V dopant in SnS2 is approximate to 4(+) but also the charge transfer (CT) from V to ligands, supported by V L-alpha,L-beta resonant inelastic X-ray scattering. These results suggest V doping produces extra interlayer covalent interactions and additional conducting channels, which increase the electronic conductivity and CT. This gives rapid transport of photo-excited electrons and effective carrier separation in layered SnS2. Additionally, valence-band photoemission spectra and S K-edge XANES indicate that the density of states near/at valence-band maximum is shifted to lower binding energy in V-doped SnS2 compare to pristine SnS2 and exhibits band gap shrinkage. These findings support first-principles density functional theory calculations of the interstitially tetrahedral O-V-S site intercalated in the vdW gap, highlighting the CT from V to ligands in V-doped SnS2.

Automated summary

The effects of electronic and atomic structures of V-doped 2D layered SnS2 were studied using X-ray spectroscopy for the development of photocatalytic/photovoltaic applications. The results showed that V doping enhances interlayer covalent interactions and additional conducting channels, leading to increased electronic conductivity and charge transfer, facilitating rapid transport of photo-excited electrons and effective carrier separation. Moreover, valence-band photoemission spectra and XANES indicated band gap shrinkage in V-doped SnS2 compared to pristine SnS2, supporting first-principles density functional theory calculations.