Delafossite-type mixed oxides A(I)B(III)O 2 prove to be thermally stable in inert or oxidizing atmospheres, but are easily degraded under reducing conditions, i.e. in molecular hydrogen. The nature of the products as well as the reaction temperatures directly depend on the metals present in the initial materials. By thermal analysis, X-ray and electron diffraction as well as electron microscopy it is shown that from selected ternary delafossites MRhO 2 (M=Cu, Ag, Pd) monophasic microcrystalline intermetallic compounds MRh can be generated at temperatures as low as ≈450 K. Similar reduction experiments are presented using novel quaternary delafossite phases CuRh x Al 1− x O 2 resp. CuRh x Cr 1− x O 2 as parent materials. A s reduction products, Cu-Rh-alloys and alumina or chromia are formed. The stoichiometry of the intermetallic products and the reduction temperatures are a function of x, where 0< x<1. The thermal stability of the intermetallic phases is characterized in inert atmosphere (N 2). By reoxidation experiments in O 2 the reversibility of the thermal reduction is studied. In addition, the thermal reactivity of the quaternary delafossite CuNi(II) 0.5Ti(IV) 0.5O 2 is described. As reduction products, metallic phases on titania are obtained.
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