4.7 Article

XPS study of iodine and tin doped Sb2S3 nanostructures affected by non-uniform charging

Journal

APPLIED SURFACE SCIENCE
Volume 567, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.apsusc.2021.150822

Keywords

X-ray photoelectron spectroscopy (XPS); Non-uniform charging; Sb2S3; Semiconductor; Energy material

Funding

  1. Ministry of Education, Science and Technological Development of the Republic of Serbia
  2. Portuguese National Funding Agency for Science, Research and Technology [UID/FIS/00068/2019]

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The study investigates the incorporation of iodine and tin into the stibnite lattice using X-ray diffraction and X-ray photoelectron spectroscopy, revealing significant effects on the surface composition and structure of the samples. The presence of different phases at the surface, such as Sb2O3 and SnS2, suggests strong segregation of antimony and surface oxidation in doped samples.
X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) measurements are used for investigating incorporation of iodine and tin into the stibnite (Sb2S3) lattice, as well as for determining surface composition and structure, respectively. The XRD analysis revealed the visible presence of a single phase, that of pure orthorhombic Sb2S3 structure. XPS survey spectra confirmed the presence of expected elements (Sb, S, Sn and I) at the surface of corresponding samples. Since the bonding identification was hindered by non-uniform charging of samples during acquiring the photoelectron spectra, a novel approach for the analysis of high resolution spectra was proposed and successfully implemented. XPS results showed that surface composition of the nondoped sample coincides with that of the bulk, while doping strongly affects surface of the samples. Sn-doped sample appears to be prone to surface oxidation. The presence of Sb2S3, Sb2O3, SnS2 and Sn(0) phases at the surface was revealed. Strong segregation of antimony was observed in the I-doped Sb2S3 sample. Iodine is also present at the surface in the form of the SbI3 phase, while the detected sulphur signal most probably corresponds to S atoms from unaltered deeper layers.

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