V. Indovina et al., The surface composition of CuOx/ZrO2 catalysts as determined by FTIR, XPS,ESR spectroscopies and volumetric CO adsorption, J PHYS CH B, 103(45), 1999, pp. 9967-9977
CuOx/ZrO2 samples prepared by adsorption from copper solutions or by impreg
nation were characterized by means of FTIR, XPS, ESR, DRS, volumetric CO ad
sorption, and redox cycles with H-2 and O-2. In samples prepared by adsorpt
ion, the maximum copper uptake corresponded to an extended plateau at 2.5 a
toms nm(-2). In as-prepared samples, isolated Cu-II species were in a disto
rted octahedral configuration, and in samples heated in dry O-2 at 773 K, i
n a square-pyramidal configuration. Water vapor adsorption transformed the
latter species into distorted octahedral complexes. In all samples, heating
in O-2 at 773 K anchored copper to the zirconia surface. All copper was pr
esent as Cu-II. Evacuation of these samples at 773 K caused no copper reduc
tion, whereas heating with H-2 above 450 K reversibly reduced Cu-II to meta
l copper. Evacuation of as-prepared samples differed according to how sampl
es were prepared. In particular, evacuation of samples prepared from Cu-ace
tylacetonate or Cu-acetate reduced Cu-II to Cu-I at 473 K and to copper met
al at higher temperature. Evacuation reduced copper because acetylacetonate
s and acetates underwent oxidation during desorption. Evacuation up to 773
K of samples prepared from Cu-nitrate caused no copper reduction. In sample
s heated in O-2 at 773 K, CO adsorption at RT yielded Cu-I-CO and carbonate
s. Volumetric CO adsorption combined with FTIR showed that copper was highl
y dispersed on the ZrO2 surface up to 2.5 atoms nm(-2).