Uncalcined TS‐2 immobilized Au nanoparticles as a bifunctional catalyst to boost direct propylene epoxidation with H2 and O2

Abstract

Developing stable yet efficient Au–Ti bifunctional catalysts is important but challenging for direct propylene epoxidation with H2 and O2. This work describes a novel strategy of employing uncalcined titanium silicalite‐2 (TS‐2‐B) to immobilize Au nanoparticles as a bifunctional catalyst for the reaction. Under no promoter effects, the Au/TS‐2‐B catalyst compared to the referenced Au/TS‐1‐B catalyst delivers outstanding catalytic performance, that is, exceptionally high stability over 100 hr, propylene oxide (PO) formation rate of 118 gPO·hr−1·kgcat−1, PO selectivity of 90% and hydrogen efficiency of 35%. The plausible relationship of catalyst structure and performance is established by using multiple techniques, such as UV–vis, high‐angle annular dark‐field scanning transmission electron microscopy, thermogravimetric analysis, and X‐ray photoelectron spectroscopy. A unique synergy of Au–Ti4+–Ti3+ triple sites is proposed for our developed Au/TS‐2‐B catalyst with the higher stable PO formation rate and hydrogen efficiency. The insights reported here could shed new light on the rational design of highly stable and efficient Au–Ti bifunctional catalysts for the reaction.