AUTHOR=Hu Mingzhen , Jin Lei , Dang Yanliu , Suib Steven L. , He Jie , Liu Ben 

TITLE=Supported Pt Nanoparticles on Mesoporous Titania for Selective Hydrogenation of Phenylacetylene

JOURNAL=Frontiers in Chemistry

VOLUME=8

YEAR=2020

URL=https://www.frontiersin.org/journals/chemistry/articles/10.3389/fchem.2020.581512

DOI=10.3389/fchem.2020.581512

ISSN=2296-2646

ABSTRACT=<p>Semi-hydrogenation of alkynes to alkenes is one of the most important industrial reactions. However, it remains technically challenging to obtain high alkene selectivity especially at a high alkyne conversion because of kinetically favorable over hydrogenation. In this contribution, we show that supported ultrasmall Pt nanoparticles (2.5 nm) on mesoporous TiO<sub>2</sub> (Pt@mTiO<sub>2</sub>) remarkably improve catalytic performance toward semi-hydrogenation of phenylacetylene. Pt@mTiO<sub>2</sub> is prepared by co-assembly of Pt and Ti precursors with silica colloidal templates <italic>via</italic> an evaporation-induced self-assembly process, followed by further calcination for thermal decomposition of Pt precursors and crystallization of mTiO<sub>2</sub> simultaneously. As-resultant Pt@mTiO<sub>2</sub> discloses a high hydrogenation activity of phenylacetylene, which is 2.5 times higher than that of commercial Pt/C. More interestingly, styrene selectivity over Pt@mTiO<sub>2</sub> remains 100% in a wide phenylacetylene conversion window (20–75%). The styrene selectivity is &gt;80% even at 100% phenylacetylene conversion while that of the commercial Pt/C is 0%. The remarkable styrene selectivity of the Pt@mTiO<sub>2</sub> is derived from the weakened styrene adsorption strength on the atop Pt sites as observed by diffuse reflectance infrared Fourier transform spectroscopy with CO as a probe molecule (CO-DRIFTS). Our strategy provides a new avenue for promoting alkyne to alkene transformation in the kinetically unfavorable region through novel catalyst preparation.</p>