First-Principles Calculations of the Effect of γ-Alumina Surface Hydroxyl Structures on the Location and Dechlorination of a Platinum Precursor.

Abstract

The interaction between Pt precursors and alumina support is an important step in synthesizing Pt/Al2O3 catalysts, while an in-depth understanding of the interaction is still lacking. Herein, density functional theory (DFT) calculations were performed to simulate the coordination of H2PtCl6 with different surface hydroxyl groups, revealing the influence of the γ-Al2O3 surface hydroxyl structure on the position of the Pt precursor and the removal of Cl ligands. After drying, the interaction mechanism between [PtCl6]2- and alumina support involves hydrogen bonds and van der Waals forces, which are the main driving forces for the structural transformation from [PtCl6]2- coordinated with the surface hydroxyl group into the PtClx(OH)y species (OH is the γ-Al2O3 surface group). HO-μ1-AlVI and H2O-μ1-AlVI on the (100) surface with electrophilicity facilitate hauling and activating the electron-rich [PtCl6]2-, but the nucleophilic (110) surface has a weaker interaction with [PtCl6]2-. Combining free energy and electronic property analysis, the stable structures on the (100) surface after drying treatment are PtCl4(OH)2 and PtCl3(OH)3, while only PtCl4(OH)2 structures can be formed on the (110) surface. This study can deepen our understanding of the interaction mechanism between Al-hydroxyl groups and Pt precursors, providing a theoretical reference for the precise placement of Pt active phases and the construction of metal-support interfaces.