RESUMO
Nanoscale zinc-oxide doped with aluminum ZnO:Al is studied by different techniques targeting surface changes induced by the conditions at which ZnO:Al is used as support material in the catalysis of methanol. While it is well established that a variety of 1H and 27Al resonances can be found by solid-state NMR for this material, it was not clear yet which signals are related to species located close to the surface of the material and which to species located in the bulk. To this end, a method is suggested that makes use of a paramagnetically impregnated material to suppress NMR signals close to the particle surface in the blind sphere around the paramagnetic metal atoms. It is shown that it is important to use conditions that guarantee a stable reference system relative to which it can be established whether the coating procedure is conserving the original structure or not. This method, called paramagnetically assisted surface peak assignment, helped to assign the 1H and 27Al NMR peaks to the bulk and the surface layer defined by the blind sphere of the paramagnetic atoms. The assignment results are further corroborated by the results from heteronuclear 27Al{1H} dipolar dephasing experiments, which indicate that the hydrogen atoms are preferentially located in the surface layer and not in the particle core.
RESUMO
The preparation of Al-doped ZnO via thermal decomposition of crystalline precursors, with a particular emphasis on kinetic effects on the solubility limits, was studied. The promoting effect of Al3+ on the catalyst system is discussed for methanol synthesis where ZnO:Al is employed as a support material for copper nanoparticles. The synthesis of the Al-doped zinc oxides in this study was inspired by the industrial synthesis of the methanol synthesis catalyst via a co-precipitated crystalline precursor, here: hydrozincite Zn5(OH)6(CO3)2. To determine the aluminium speciation and the solubility limit of the aluminium cation on zinc positions, a series of zinc oxides with varying aluminium contents was synthesized by calcination of the precursors. Short precipitate ageing time, low ageing temperature and aluminium contents below 3 mol% metal were advantageous to suppress crystalline side-phases in the precursor, which caused an aluminium segregation and non-uniform aluminium distribution in the solid. Even if zinc oxide was the only crystalline phase, TEM revealed such segregation in samples calcined at 320 °C. Only at very low aluminium contents, the dopant was found preferably on the zinc sites of the zinc oxide structure based on the signal dominating the 27Al NMR spectra. The solubility limit regarding this species was determined to be approximately xAl = 0.013 or 1.3% of all metal cations. Annealing experiments showed that aluminium was kinetically trapped on the site and segregated into ZnAl2O4 upon further heating. This shows that lower calcination temperatures such as applied in catalyst synthesis conserve a higher aluminium doping concentration on that specific site than is expected thermodynamically.
