Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/72961
Type: Artigo de periódico
Title: X-ray photoelectron spectroscopic study of rare-earth-doped amorphous silicon-nitrogen films
Author: Zanatta, AR
Ribeiro, CTM
Alvarez, F
Abstract: Amorphous silicon-nitrogen (a-SiN) films independently doped with different rare-earth (RE) elements (Y, La, Pr, Nd, Sm, Gd, Tb, Dy, Ho, Er, Tm, Yb, and Lu) have been prepared by cosputtering. The films were investigated in detail by x-ray photoelectron spectroscopy employing 1486.6 eV photons. Additional information was also achieved by optical techniques and ion beam analyses. As a result of the deposition method and conditions, the films present similar contents of Si and N, and rare-earth concentrations below 1.0 at. %. In spite of this relatively low concentration, and taking advantage of the high photoionization cross section of the rare-earth elements at 1486.6 eV, the signal of several different core-levels and Auger transitions could be detected and analyzed. The electronic states at the top of the valence band of the RE-doped a-SiN films were also investigated with 1486.6 eV photons. Compared to the spectroscopic data of pure metals, the RE-related core levels of the present a-SiN films exhibit an energy shift typically in the 0.8-2.5 eV range, which is attributed to the presence of nitrogen atoms. According to the experimental data, most of the RE ions remain in the 3+ state. The only clear exception occurs in the Yb-doped a-SiN film, where a large fraction of Yb2+ coexisting with Yb3+ ions is evident. (C) 2003 American Institute of Physics.
Country: EUA
Editor: Amer Inst Physics
Rights: aberto
Identifier DOI: 10.1063/1.1536015
Date Issue: 2003
Appears in Collections:Artigos e Materiais de Revistas Científicas - Unicamp

Files in This Item:
File Description SizeFormat 
WOS000180702400016.pdf772.22 kBAdobe PDFView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.