Lin, Dong, Feng, Xiang, Xu, Yang, Lewis, Richard J., Chen, Xiao, Davies, Thomas E., Pattisson, Samuel, Douthwaite, Mark, Yin, Defu, He, Qiuming, Zheng, Xiuhui, Chen, De, Yang, Chaohe and Hutchings, Graham J. ![]() ![]() |
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Abstract
The development of titianosilicates is considered a major milestone in oxidative catalysis due to the ability of framework Ti sites to co-ordinate hydrogen peroxide/peroxy species. Herein, we demonstrate that interfacial Ti sites can be constructed through the vertical intergrowth of two MFI-type zeolite surfaces along [100] and [010] projections, with the assistance of UV-induced hydroxyl radicals. The application of these intergrown titanosilicalites as supports for Au species are observed to simultaneously offer a 2.1-fold and 3.0-fold increase in propene oxide (PO) formation rate and Au efficiency, respectively, when compared to standard Au/TS-1 catalysts. Mechanistic studies reveal that the intergrown interface Ti sites allow for lower-energy epoxidation pathways with more efficient activation of key oxygen-transfer intermediates. These results provide insights into the development of zeolite intergrown interface sites (e.g., titanosilicalite/silicalite-1/ZSM-5) and may allow for further advancements in the epoxidation of a range of key feedstocks.
Item Type: | Article |
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Date Type: | Published Online |
Status: | Published |
Schools: | Schools > Chemistry Research Institutes & Centres > Cardiff Catalysis Institute (CCI) |
Additional Information: | License information from Publisher: LICENSE 1: URL: http://creativecommons.org/licenses/by/4.0/, Type: open-access |
Publisher: | Nature Research |
ISSN: | 2041-1723 |
Date of First Compliant Deposit: | 7 July 2025 |
Date of Acceptance: | 30 May 2025 |
Last Modified: | 07 Jul 2025 13:15 |
URI: | https://orca.cardiff.ac.uk/id/eprint/179595 |
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