Zeolite Synthesis in the Presence of Metallosiloxanes for the Quantitative Encapsulation of Metal Species for the Selective Catalytic Reduction (SCR) of NOx

Abstract Metal encapsulation in zeolitic materials through one‐pot hydrothermal synthesis (HTS) is an attractive technique to prepare zeolites with a high metal dispersion. Due to its simplicity and the excellent catalytic performance observed for several catalytic systems, this method has gained a great deal of attention over the last few years. While most studies apply synthetic methods involving different organic ligands to stabilize the metal under synthesis conditions, here we report the use of metallosiloxanes as an alternative metal precursor. Metallosiloxanes can be synthesized from simple and cost‐affordable chemicals and, when used in combination with zeolite building blocks under standard synthesis conditions, lead to quantitative metal loading and high dispersion. Thanks to the structural analogy of siloxane with TEOS, the synthesis gel stabilizes by forming siloxane bridges that prevent metal precipitation and clustering. When focusing on Fe‐encapsulation, we demonstrate that Fe‐MFI zeolites obtained by this method exhibit high catalytic activity in the NH 3 ‐mediated selective catalytic reduction (SCR) of NO x along with a good H 2 O/SO 2 tolerance. This synthetic approach opens a new synthetic route for the encapsulation of transition metals within zeolite structures.