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<HTML> <HEAD> <META HTTP-EQUIV="Content-Type" CONTENT="text/html; charset=utf-8"> <META NAME="Generator" CONTENT="Microsoft Word 97"> <TITLE>Joint Semiconductors Surface Study group</TITLE> <META NAME="Template" CONTENT="C:\PROGRAM FILES\MICROSOFT OFFICE\OFFICE\html.dot"> </HEAD> <BODY LINK="#0000ff" VLINK="#800080" BACKGROUND="Background.jpg"> <FONT SIZE=4><P>L.V.Yashina, E.V.Tikhonov, V.S.Neudachina, T.S.Zyubina, A.N.Chaika, V.I.Shtanov, S.P.Kobeleva, Yu.A. Dobrovolsky. The oxidation of PbTe(100) surface in dry oxygen. <I>Surface and Interface Analysis, </I>2004 (in press)</P> <P>Abstract</P> <P>The oxidation of PbTe (100) surface in dry oxygen was studied by means of XPS. The appearance of a Te<SUP>4+ </SUP>component in Te3d spectra and an additional component shifted to 1 eV in Pb 4f spectra was observed. It was revealed that at exposures 10<SUP>11</SUP>-10<SUP>15</SUP>L the oxidation mechanism does not change. The oxidation product stoichiometry is close to PbTeO<SUB>3</SUB>. Quantum chemical modelling of the interaction of small cluster (PbTe)<SUB>4</SUB> with one oxygen molecule was performed in the frames of density functional theory (B3LYP). It was revealed that Pb-O (2.22-2.43Å) and Te-O (1.97Å) bonds are formed during the energetically favorable chemisorption process, this leading to the increase of Pb and Te effective Mulliken charges by +0.18-0.31e and +1.11e, respectively. These changes are in good correlation with the observed binding energies for additional components in the XPS spectra of the oxidized surface.</P></FONT></BODY> </HTML>
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