posted on 2018-02-13, 00:00authored byRuohong Sui, John M. H. Lo, Christopher B. Lavery, Connor E. Deering, Kyle G. Wynnyk, Nancy Chou, Robert A. Marriott
Two-dimensional (2D) metal oxide
nanostructures have generated a great deal of attention in material
science for their prospective wide-ranging applications; therefore,
a scalable and economical method for producing these structures is
an asset. In this research, a simple procedure for the preparation
of 2D aluminum hydroxide acetate macromolecules ([Al(OH)(OAc)2]m) has been developed via a nonaqueous
sol–gel route at a mild reaction temperature and ambient pressure.
To gain a greater understanding of the mechanism for how the self-assembly
of these 2D structures occurs, a combination of in situ Fourier transform
infrared (FTIR) measurements and density functional theory (DFT) calculations
were utilized. It was found that the bridging OH–1 and coordination modes of the organic ligands guide the assembly
of the planar nanostructures. The theoretical calculation results
show that the structures of the [Al(OH)(OAc)2]8 oligomer can be either a linear or a planar structure, and the
latter is more thermodynamically favorable than its linear counterpart.
The simple synthesis method described herein could possibly open a
new avenue for designing 2D nanostructures via ligand-directed anisotropic
condensation reactions.