MIL-101(Cr) entrapped polyol-synthesized iron promoted platinum bimetallic nanoparticles system for synergistic selective hydrogenation of cinnamaldehyde

The interfacial characteristics of platinum (Pt) metal catalysts can be systematically regulated by interacting them with electropositive metals, leading to synergistic interactions for extensive catalytic applications. In this study, an evenly dispersed polyol-synthesized iron (Fe)-promoted Pt bimetallic nanoparticle (BNPs) system was embedded in MIL-101(Cr). The PtFe₂@MIL-101(Cr) catalyst unveiled remarkable activity (86%) and selectivity (89%) for the superior hydrogenation of the targeted C[dbnd]O bond of cinnamaldehyde (CAL). The exceptional hydrogenation performance can be credited to the interplay of the geometric and electronic properties arising from charge shuttling between Fe and Pt within the homogenously distributed Pt–Fe bimetallic nanoparticle system. The experimental results indicate enhanced valence electrons in the Pt d-band through the mutual synergetic interface between the Pt and Fe BNPs. Consequently, these Fe–Pt sites functioned as interfacial electrophilic and nucleophilic (Lewis acid-base) sites, enhancing H₂ activation and facilitating C[dbnd]O bond conversion to yield unsaturated cinnamal alcohols (COL). Additionally, the narrow pores of MIL-101(Cr) encapsulating the Pt–Fe BNPs induced steric hindrance, allowing only C[dbnd]O bond hydrogenation. Furthermore, the PtFe₂@MIL-101(Cr) catalyst maintained its optimal hydrogenation performance over five cycles, demonstrating no substantial loss in either CAL conversion or COL yield, thus endorsing the universal practical applicability of the catalyst.