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Palladium Encapsulated by an Oxygen‐Saturated TiO 2 Overlayer for Low‐Temperature SO 2 ‐Tolerant Catalysis during CO Oxidation
The development of oxidation catalysts that are resistant to sulfur poisoning is crucial for extending the lifespan of catalysts in real‐working conditions. Herein, we describe the design and synthesis of oxide‐metal interaction (OMI) catalyst under oxidative atmospheres. By using organic coated TiO...
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Published in: | Angewandte Chemie International Edition 2023-12, Vol.62 (49) |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The development of oxidation catalysts that are resistant to sulfur poisoning is crucial for extending the lifespan of catalysts in real‐working conditions. Herein, we describe the design and synthesis of oxide‐metal interaction (OMI) catalyst under oxidative atmospheres. By using organic coated TiO
2
, an oxide/metal inverse catalyst with non‐classical oxygen‐saturated TiO
2
overlayers were obtained at relatively low temperature. These catalysts were found to incorporate ultra‐small Pd metal and support particles with exceptional reactivity and stability for CO oxidation (under 21 vol % O
2
and 10 vol % H
2
O). In particular, the core (Pd)‐shell (TiO
2
) structured OMI catalyst exhibited excellent resistance to SO
2
poisoning, yielding robust CO oxidation performance at 120 °C for 240 h (at 100 ppm SO
2
and 10 vol % H
2
O). The stability of this new OMI catalyst was explained through density functional theory (DFT) calculations that interfacial oxygen atoms at Pd−O−Ti sites (of oxygen‐saturated overlayers) serve as non‐metal active sites for low‐temperature CO oxidation, and change the SO
2
adsorption from metal(d)‐to‐SO
2
(π*) back‐bonding to much weaker σ(Ti−S) bonding. |
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ISSN: | 1433-7851 1521-3773 |
DOI: | 10.1002/anie.202310191 |