XAS characterization of the RuO2-Ta2O5 system local (crystal) structure

Autor(es)

Ribeiro, Josimar ^{[1, 2]} ; Tremiliosi-Filho, Germano ^[3] ; Olivi, Paulo ^[1] ; de Andrade, Adalgisa R. ^[1]

Afiliação do(s) autor(es)

^[1] Univ Sao Paulo, Fac Filosofia Ciencias & Letras Ribeirao Preto, Dept Quim, BR-14040901 Ribeirao Preto, SP - Brazil

^[2] Univ Fed Espirito Santo, Ctr Ciencias Exatas, Dept Quim, BR-29075910 Vitoria, ES - Brazil

^[3] USP, Inst Quim Sao Carlos, Sao Carlos, SP - Brazil

• Tipo de documento: Artigo Científico
• Fonte: Materials Chemistry and Physics; v. 125, n. 3, p. 449-460, FEB 15 2011.
• Citações Web of Science: 9

Resumo

The influence of the preparation method on the structural properties of the RuO(2)-Ta(2)O(5) system was investigated. Both thin films on Ti substrates and powder samples of nominal composition Ti/RuO(2)-Ta(2)O(5) (Ru:Ta = 100:0, 90:10, 80:20, 30:70, and 0:100 at.%) were prepared through thermal decomposition of polymeric precursors (DPP). The thin films and powder samples were investigated using X-ray absorption spectroscopy (XAS). XANES analyses showed that Ru and Ta are present in the Ru(IV) and Ta(V) oxidation states. EXAFS signals of all the samples were analyzed, to obtain the average bond length (r), coordination number, and the Debye-Waller factor (sigma(2)) for each Ru-O, Ru-Ru, Ta-O nearest-neighbor. The first shell Ru-O distance was found at 1.91-1.92 angstrom with coordination number of 1.8-2.1, and at 2.01-2.02 angstrom with coordination number of 3.9-4.1. The Ta-O distance obtained for all the samples and in both modes (transmission and fluorescence) had significantly different values from the theoretical ones. The results revealed that the local structure around both the Ru and Ta sites are similar, and that they consist of distorted M-O(6) octahedra (where M = Ru or Ta). (C) 2010 Elsevier B.V. All rights reserved. (AU)

• Processo FAPESP: 02/06465-0 - Estudo de eletrodos óxidos binários de decomposição RuO2-Ta2O5: investigação da oxidação de etanol e ácido acético em meio ácido como reações modelo da quebra da ligação C-C
• Beneficiário: Josimar Ribeiro
• Modalidade de apoio: Bolsas no Brasil - Doutorado