4.8 Article

Boosting toluene oxidation by the regulation of Pd species on UiO-66: Synergistic effect of Pd species

Journal

JOURNAL OF CATALYSIS
Volume 413, Issue -, Pages 59-75

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcat.2022.06.015

Keywords

Single Pd atom; Restructuring; Pyridinic N; Pd1-N-1 structure; Synergistic effect

Funding

  1. National Natural Science Foundation of China [12175145]
  2. Shanghai Rising-Star Program [21QA1406600]
  3. Natural Science Foundation of Shanghai [19ZR1434900]

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Supported single-atoms and sub-nanometre clusters have shown excellent catalytic performance in many reactions, but they are prone to inactivation in complex reactive conditions. This study demonstrates that Pd-UiO-66 catalyst with ultra-low Pd loading contains active Pd species (isolated Pd atom, sub-nanometre Pd clusters, and Pd nanoparticles), and exhibits superb activity for toluene oxidation and water resistance.
Supported single-atoms and sub-nanometre clusters have exhibited superb catalytic performance toward many reactions. However, inactivation of single-atom or cluster catalysts in complex reactive conditions poses major challenge for their practical application. Herein, we demonstrate that the prepared Pd-UiO-66 with ultra-low Pd loading (0.05 wt%) contains three robust active Pd species, (isolated Pd atom (Pd1), sub-nanometre Pd clusters (Pdc) and Pd nanoparticles (Pdn)) and presents superb activity for toluene oxidation and water resistance (10.0 vol%). Experiments and theoretical calculations firstly confirm that con-secutive H-2-O-2 and reaction gas treatment (1000 ppm toluene in 20 vol.%O-2/Ar) induce residual N species from solvent N, N-dimethylformamide to enter UiO-66 skeleton forming Pd1-N1 structures. DFT calculations reveal that the synergistic effect of Pd species (namely, the enhanced activation of O-2 and H2O by Pd1 and the improved adsorption of toluene by Pdc and Pdn) is the main factor for the excellent activity of Pd-U-H-O-reused catalyst. (C) 2022 Elsevier Inc. All rights reserved.

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