Study of the structure of niobium oxide by X-ray absorption fine structure and surface science techniques

Abstract

The structure of niobium oxides was investigated by using XAFS and surface science techniques. The origin of acidic property and catalysis of niobium oxide is discussed by these results. From the EXAFS analysis, the structure of highly acidic hydrated niobium oxide is different from those of T-Nb 2O 5 and K 8Nb 6O 19, which has been previously demonstrated as the structure of hydrated niobium oxide, because NbNb and NbO distances are significantly different from each other. There are at least two types of NbO bonds, a tetrahedral form and an octahedral form are existing for hydrated niobium oxide. The excess of negative charge is present for NbO bond by applying Tanabe's hypothesis to single metal oxide consisting of at least two metal-O forms with different coordination number. That seems to be the origin of the acidity of hydrated niobium oxide. The ordered niobium oxides thin film on Pt(111) and their defect face were prepared by using UHV surface analysis apparatus. The oxygen vacancies of niobium oxide on Pt(111) were created by Ar +ion bombardment. H 2O and CH 3OH exhibit associated adsorption on the ordered NbO x and Nb 2O 5 surface and dissociative adsorption on the defect Nb 2O 5 surface at room temperature. On the ordered NbO x and Nb 2O 5 surface, no evidence of ethene adsorption at 200 K is found by HREELS, although ethene adsorbs molecularly on the defect Nb 2O 5 surface with a π-complex formation. These results imply that oxygen vacancies of NbO x surface play an important role on the adsorption of the molecules.