Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

Owing to their vast chemical and structural flexibility, layered double hydroxides (LDHs) are among some of the most promising materials for many catalytic applications. Thermal decomposition below 700 °C leads to the formation of a complex semiamorphous mixed metal oxide (LDO). In this study, the product of calcination of aqueous miscible organic solvent-treated AMO-[Mg0.70Al0.30(OH)2]­(CO3)0.15·yH2O·zEtOH at 600 °C (AMO-Mg2.33Al LDO) has been investigated using a synergistic combination of high-resolution synchrotron X-ray and neutron scattering techniques, as well as high-angle annular dark-field scanning transmission electron microscopy (HAADF-STEM), solid-state NMR (ssNMR), and thermogravimetric analysis coupled with mass spectrometry (TGA-MS). The local and extended structure of AMO-Mg2.33Al LDO has been modeled by reciprocal and real space X-ray and neutron scattering analyses and is consistent with a modified rock salt structure consisting of octahedrally coordinated layers containing a small number of vacancies and the tetrahedrally coordinated Al3+ sites in contrast to previous reports.

More information Original publication

DOI

10.1021/acs.inorgchem.5c03754

Type

Journal article

Publisher

American Chemical Society

Publication Date

2025-11-10T00:00:00+00:00

Volume

64

Pages

22720 - 22728

Total pages

8