4.6 Article

In Situ Observation of ZnO Nanoparticle Formation by a Combination of Time-Resolved X-ray Absorption Spectroscopy and X-ray Diffraction

Journal

MATERIALS
Volume 15, Issue 22, Pages -

Publisher

MDPI
DOI: 10.3390/ma15228186

Keywords

Zn-oxide synthesis; in situ investigation; solution chemistry; X-ray absorption spectroscopy; X-ray diffraction

Funding

  1. German Academic Exchange Service, DAAD [57514145]
  2. German Federal Ministry of Education and Research [05K19PXA]

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This study investigates the formation of ZnO nanomaterials from different Zn acetylacetonate precursor solutions under different temperature and solvent conditions using X-ray diffraction and X-ray absorption spectroscopy. The results show that the efficiency and crystal orientation of ZnO formation are strongly influenced by the reaction temperature and solvent type.
The formation of ZnO nanomaterials from different Zn acetylacetonate precursor solutions was studied in situ by employing simultaneous, time-resolved X-ray diffraction (XRD) and X-ray absorption spectroscopy (EXAFS) at the Zn K-edge. The precursor solutions were heated from room temperature to the desired reaction temperatures in a hermetically sealed cell dedicated to X-ray experiments. In general, the first indications for the formation of hexagonal ZnO were found for elevated temperatures of about 80 degrees C both by XRD and EXAFS, and the contributions increase with temperature and time. However, no reaction intermediates could be proved in addition to the Zn precursors and the formed hexagonal ZnO materials. Furthermore, the results show that the efficiency of the reaction, i.e., the conversion of the precursor material to the ZnO product, strongly depends on the solvent used and the reaction temperature. ZnO formation is accelerated by an increased temperature of 165 degrees C and the use of 1-octanol, with a conversion to ZnO of more than 80% after only a ca. 35 min reaction time according to a detailed analysis of the EXAFS data. For comparison, an identical concentration of Zn acetylacetonate in water or dilute alkaline NaOH solutions and a reaction temperature of around 90 degrees C leads to a smaller conversion of approximately 50% only, even after several hours of reaction. The particle size determined from XRD for different orientations shows a preferred orientation along the c-direction of the hexagonal crystal system, as well in accordance with scanning electron microscopy. The LaMer model explained this highly non-uniform growth of needle-like ZnO crystallites.

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