In Situ Incorporation of Atomically Precise Au Nanoclusters within Zeolites for Ambient Temperature CO Oxidation

Author:

Tesana Siriluck123,Kennedy John V.23ORCID,Yip Alex C. K.24ORCID,Golovko Vladimir B.12ORCID

Affiliation:

1. School of Physical and Chemical Sciences, University of Canterbury, Christchurch 8041, New Zealand

2. The MacDiarmid Institute for Advanced Materials and Nanotechnology, Wellington 6140, New Zealand

3. National Isotope Centre, GNS Science, Lower Hutt 5010, New Zealand

4. Department of Chemical and Process Engineering, University of Canterbury, Christchurch 8041, New Zealand

Abstract

Preserving ultrasmall sizes of metal particles is a key challenge in the study of heterogeneous metal-based catalysis. Confining the ultrasmall metal clusters in a well-defined crystalline porous zeolite has emerged as a promising approach to stabilize these metal species. Successful encapsulation can be achieved by the addition of ligated metal complexes to zeolite synthesis gel before hydrothermal synthesis. However, controlling the metal particle size during post-reduction treatment remains a major challenge in this approach. Herein, an in situ incorporation strategy of pre-made atomically precise gold clusters within Na-LTA zeolite was established for the first time. With the assistance of mercaptosilane ligands, the gold clusters were successfully incorporated within the Na-LTA without premature precipitation and metal aggregation during the synthesis. We have demonstrated that the confinement of gold clusters within the zeolite framework offers high stability against sintering, leading to superior CO oxidation catalytic performance (up to 12 h at 30 °C, with a space velocity of 3000 mL g−1 h−1).

Funder

University of Canterbury

MacDiarmid Institute for Advanced Materials and Nanotechnology

Publisher

MDPI AG

Subject

General Materials Science,General Chemical Engineering

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