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dc.creatorGržetić, Ivan
dc.creatorŽunic, T.B.
dc.date.accessioned2018-11-22T00:00:39Z
dc.date.available2018-11-22T00:00:39Z
dc.date.issued1993
dc.identifier.issn0342-1791
dc.identifier.urihttp://cherry.chem.bg.ac.rs/handle/123456789/35
dc.description.abstractThe results of X-ray induced photoelectron spectroscopy (XPS) experiments on several phases of the ternary system Tl-Sb-S are reported. The binding energies of the inner S, Sb and Tl electrons increase with increasing quantities of Sb and decreasing amounts of Tl in these compounds. This is explained by the influences of the proportions of the bonded metals on the effective electron affinity of S. The higher proportions of the more electronegative element bonded to S cause the increase of its effective electron affinity. The results for Tl2S (carlinite), Tl3SbS3, TlSbS2 (weissbergite), TlAsS2 (lorandite) and Sb2S3 (antimonite) can be interpreted in this way. The results for Tl4S3 suggest a predominantly covalent character of bonding for both Tl(III) and Tl(I), which are present in this sulfide. From comparison with Tl3SbS4 it could be supposed that Tl(III)-S bond has a more covalent character than Sb(V)-S bond. The results for Tl3SbS4 are in agreement with crystal structure data and the results of Moessbauer spectroscopy. For AsS (realgar) the binding energies of the inner electrons of As and S significantly increase, showing that the electrons in molecular orbitals are less strongly bonded to individual atoms, as compared to pure elements. The results for the amorphous TlSb5S8 (corresponding in composition to parapierrotite) suggest that in amorphous compound the Tl-S bonding is stronger and the coordination of Tl more regular than in a crystalline one. © 1993 Springer-Verlag.en
dc.rightsrestrictedAccess
dc.sourcePhysics and Chemistry of Minerals
dc.titleThe photoelectron spectra of some Tl-Sb sulphosaltsen
dc.typearticle
dc.rights.licenseARR
dc.citation.volume20
dc.citation.issue4
dc.citation.spage285
dc.citation.epage296
dc.identifier.doi10.1007/BF00208142
dc.citation.other20(4): 285-296
dc.identifier.scopus2-s2.0-0027842371
dc.identifier.rcubKon_1016


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