Published March 2022 | Version Supplemental Material
Journal Article Open

Mesoporous silica stabilized MOF nanoreactor for highly selective semi-hydrogenation of phenylacetylene via synergistic effect of Pd and Ru single site

  • 1. ROR icon China University of Petroleum, Beijing
  • 2. ROR icon Shanghai University
  • 3. ROR icon California Institute of Technology

Abstract

Selective semi-hydrogenation of phenylacetylene to styrene is a crucial step in the polystyrene industry. Although Pd-based catalysts are widely used in this reaction due to their excellent hydrogenation activity, the selectivity for styrene remains a great challenge. Herein, we designed a mesoporous silica stabilized Pd-Ru@ZIF-8 (MS Pd-Ru@ZIF-8) nanoreactor with novel Pd and Ru single site synergistic catalytical system for semi-hydrogenation of phenylacetylene. The nanoreactor exhibited a superior performance, achieving 98% conversion of phenylacetylene and 96% selectivity to styrene. Turnover frequency (TOF) of nanoreactor was up to as high as 2,188 h⁻¹, which was 25 times and 5 times more than the single metal species catalysts, mesoporous silica stabilized Pd@ZIF-8 nanoreactor (MS Pd@ZIF-8), and mesoporous silica stabilized Ru@ZIF-8 nanoreactor (MS Ru@ZIF-8). This catalytic activity was attributed to the synergistic effect of Pd and Ru single site anchored strongly into the framework of ZIF-8, which reduced the desorption energy of styrene and increased the hydrogenation energy barrier of styrene. Importantly, since the ordered mesoporous silica was introduced into the nanoreactor shell to stabilize ZIF-8, MS Pd-Ru@ZIF-8 showed excellent reusability and stability. After the five cycles, the catalytical activity and selectivity still remained. This work provides insights for a synergistic catalytic system based on single-site active sites for selective hydrogenation reactions.

Additional Information

© Tsinghua University Press and Springer-Verlag GmbH Germany, part of Springer Nature 2021. Received 17 May 2021; Revised 27 August 2021; Accepted 30 August 2021; Published 30 September 2021. We gratefully acknowledge the financial support from the Beijing Natural Science Foundation (No. 2182061) and Science Foundation of China University of Petroleum, Beijing (No. 2462019BJRC001).

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Additional details

Identifiers

Eprint ID
112069
DOI
10.1007/s12274-021-3849-2
Resolver ID
CaltechAUTHORS:20211129-203859601

Related works

Funding

Beijing Natural Science Foundation
2182061
Science Foundation of China University of Petroleum
2462019BJRC001

Dates

Created
2021-11-29
Created from EPrint's datestamp field
Updated
2022-03-02
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