AI Article Synopsis
- An in situ method has been developed for growing ZnO nanocrystals on Zn/Al mixed metal oxide surfaces, utilizing thermal treatment of layered double hydroxides (LDHs) with nitrate ions.
- The process involves the partial separation of the LDH structure, allowing ZnO crystals to form on the MMO layers, which was confirmed through various analytical techniques including thermogravimetry, mass spectrometry, and X-ray diffraction.
- Different fractions of nitrate and external sources like ammonium nitrate influence the size and quantity of ZnO nanoparticles, enabling customization of their characteristics during the synthesis process.
Article Abstract
An in situ method for the growth of ZnO nanocrystals on Zn/Al mixed metal oxide (MMO) surfaces is presented. The key to this method is the thermal treatment of Zn/Al layered double hydroxides (Zn/Al LDHs) in the presence of nitrate anions, which results in partial demixing of the LDH/MMO structure and the subsequent crystallization of ZnO crystals on the surface of the forming MMO layers. In a first experimental series, thermal treatment of Zn/Al LDHs with different fractions of nitrate and carbonate in the interlayer space was examined by thermogravimetry coupled with mass spectrometry (TG-MS) and in situ XRD. In a second experimental series, Zn/Al LDHs with only carbonate in the interlayer space were thermally treated in the presence of different amounts of an external nitrate source (NH4NO3). All obtained Zn/Al MMO samples were analysed by electron microscopy, nitrogen physisorption and powder X-ray diffraction. The gas phase formed during nitrate decomposition turned out to be responsible for the formation of crystalline ZnO nanoparticles. Accordingly, both interlayer nitrate and the presence of ammonium nitrate led to the formation of supported ZnO nanocrystals with mean diameters between 100 and 400 nm, and both methods offer the possibility to tailor the amount and size of the ZnO crystals by means of the amount of nitrate.
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| http://dx.doi.org/10.1002/chem.201304484 | DOI Listing |
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