Structure Sensitivity of Acetylene Semi-Hydrogenation on Pt Single Atoms and Subnanometer Clusters

Journal Article (Journal Article)

Oxide-supported Pt-group single atoms and clusters in the subnanometer size regime maximize the metal utilization and have shown extraordinary catalytic properties for many reactions including selective hydrogenation. Establishing relations between the metal nuclearity and electronic and catalytic properties is crucial for catalyst design. Here, we varied the nuclearity of Pt supported on TiO from single atoms to subnanometer clusters to larger nanoparticles to develop such relations for acetylene hydrogenation. We show that, in contrast to the low selectivity on large Pt nanoparticles, in the subnanometer size regime, Pt exhibits remarkably high selectivity to ethylene. Through a combination of X-ray photoelectron spectroscopy and calorimetry, we demonstrate that the origin of high selectivity is the decreased electron density on Pt and destabilization of C H as the Pt nuclearity decreases. However, as the Pt nuclearity decreased, the activity for H activation and acetylene hydrogenation decreased, indicating a trade-off between activity and selectivity. The results show that, while different properties emerge in the subnanometer regime, Pt supported on TiO appears to be bound by similar scaling and Brønsted-Evans-Polanyi relationships as on metal surfaces. 2 2 4 2 2

Full Text

Duke Authors

Cited Authors

  • Kuo, CT; Lu, Y; Kovarik, L; Engelhard, M; Karim, AM

Published Date

  • January 1, 2019

Published In

Start / End Page

  • 11030 - 11041

Electronic International Standard Serial Number (EISSN)

  • 2155-5435

Digital Object Identifier (DOI)

  • 10.1021/acscatal.9b02840

Citation Source

  • Scopus