Tuning cluster size down to single atoms on Pt/γ-Al2O3 catalysts via surface organometallic chemistry

Abstract

Platinum catalysts supported on γ-Al2O3 are central to a variety of applications. The conditions controlling the formation of Pt single atoms and subnanometric clusters remain elusive. The present work based on surface organometallic chemistry (SOMC) unravels their formation under oxidative and reductive atmospheres. Following the grafting of MeCpPtMe3 as a molecular precursor to generate highly dispersed sites on alumina, the evolution upon thermal treatment under oxidative or reductive conditions is monitored by in situ FTIR, with the ultimate goal to access catalysts with different single atom over cluster ratio, comparing SOMC with a conventional preparation method. Under oxidative atmosphere, all ligands are removed to form CO2 in a multi-step process, while under reductive conditions, ligands likely decompose through hydrogenolysis/hydrogenation reactions. HAADF-STEM characterization and CO adsorption experiments reveal the presence of several states of Pt, depending on the Pt surface density and the treatment applied. Under reductive atmosphere, the size of platinum clusters remains relatively constant and lower than 0.8 nm, regardless of the Pt surface density (0.03-0.09-0.15 Pt/nm2). Under oxidative atmosphere, the Pt surface density is a key factor that drives the size of platinum clusters and the relative amount of single atoms, both significantly different from that of a reference conventional catalyst obtained by incipient wetness impregnation of Pt(NH3)4(NO3)2. Notably, the material at 0.03 Pt/nm² exhibits mainly Pt single atoms after calcination, while increasing Pt density favors cluster formation.