Dynamic boron-doping switched chitin-based single-atom Pt catalyst for chemo-selective hydrogenation

Biomass valorization is a way to promote the ‘waste-to-wealth’ concept, which is a pre-requisite condition for a future sustainable lifestyle. The direct utilization of natural polymer for value-added materials should be prioritized. With this object, we demonstrate a facile and economical method to...

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Published inNature communications Vol. 16; no. 1; pp. 2296 - 9
Main Authors Li, Yan, Lu, Lijun, Jiang, Xueyu, Yang, Dali, Chen, Jeng-Lung, Dutta Chowdhury, Abhishek, Li, Wu, Pei, Xianglin, Lei, Aiwen
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 07.03.2025
Nature Publishing Group
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Summary:Biomass valorization is a way to promote the ‘waste-to-wealth’ concept, which is a pre-requisite condition for a future sustainable lifestyle. The direct utilization of natural polymer for value-added materials should be prioritized. With this object, we demonstrate a facile and economical method to prepare chitin-derived supramolecular nanowires-stabilized single-atom sites Pt catalysts (SS-Pt-CSNs). A comprehensive characterization shows the structure of single-atom Pt coordinated with the organic supramolecular (ligand-type) entity, which is both flexible (like in homogenous catalyst) and robust (like in heterogenous catalyst). Such hybrid characteristics of these SS-Pt-CSNs materials exhibit excellent catalytic performance for chemo-selective hydrogenation of various unsaturated bonds with a selectivity of more than 90:1 and a high turnover number (TON) of 121,350. Mechanistic studies demonstrate that both empty coordination sites of Pt and dynamic B-doping are the key factors for exceptional efficiency and high selectivity. Biomass valorization is a way to promote the ‘waste-to-wealth’ concept, which is a prerequisite condition for a future sustainable lifestyle. Here, the authors demonstrate a methodology to prepare chitin-derived supramolecular nanowires-stabilized single-atom site platinum catalysts.
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ISSN:2041-1723
2041-1723
DOI:10.1038/s41467-025-57434-0