4.8 Article

In situ total scattering experiments of nucleation and crystallisation of tantalum-based oxides: from highly dilute solutions via cluster formation to nanoparticles

Journal

NANOSCALE
Volume 13, Issue 1, Pages 150-162

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d0nr07871a

Keywords

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Funding

  1. International Max Planck Research School for Interface Controlled Materials for Energy Conversion (IMPRS-SurMat)
  2. MAXNET Energy consortium of Max Planck Society
  3. Alexander von Humboldt Foundation through Humboldt Research Fellowships
  4. Max Planck Society

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The structural evolution of tantalum-based oxides was studied from the formation of hydrolysed clusters to temperature-induced crystallisation processes, providing insight on the connectivity, arrangement, and size of clusters as well as the transformation into crystalline orthorhombic L-Ta2O5 without intermediate structures.
The exact formation mechanism of tantalum oxides (and in general, metal/mixed metal oxides) from alkoxide precursors is still not fully understood, particularly when forming cluster-like or amorphous materials. The structural evolution of Ta-based oxides was studied in detail using X-ray total scattering experiments along with subsequent pair distribution function (PDF) analyses. Starting from a tantalum alkoxide precursor (Ta-2(OEt)(10)), the formation of hydrolysed TaxOyHz clusters in highly diluted aqueous solution was analysed. From the PDF data, the connectivity and arrangement of TaxOy octahedra in the cluster could be deduced as well as the approximate size of the clusters (<1 nm). Construction of cluster models allowed for identification of common structural motifs in the TaxOyHz clusters, ruling out the formation of chain- or ring-like clusters. More likely, bulky clusters with a high number of corner-sharing octahedra are formed. After separation of the amorphous solid from the liquid, temperature-induced crystallisation processes were monitored via in situ total scattering experiments. Between room temperature and 600 degrees C, only small rearrangements of the amorphous structure are observed. At about 610 degrees C, amorphous TaxOyHz transforms directly into crystalline orthorhombic L-Ta2O5 without formation of any crystalline intermediate structures.

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