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Understanding the dynamic evolution of heterogeneous catalysts is crucial yet challenging for elucidating the structure-performance relationships and enabling rational catalyst design. Herein, we reveal that PtIn alloy clusters gradually evolve into PtIn intermetallic in response to propylene, the product of propane dehydrogenation (PDH) reaction. Specifically, a PtIn/SiO catalyst has been fabricated, comprising sub-nanometric PtIn alloy clusters covered by an In overlayer, with In species locating at the metal-support interface. During the PDH reaction propylene induces the evaporation of the In overlayer, thereby exposing Pt sites. After an induction period, the evolved PtIn intermetallic (average size ~1.3 nm) exhibits a CH productivity of 145 mol g h. The alloyed In species effectively dilute Pt-Pt ensembles, enhancing propylene selectivity, while the interfacial In species inhibit aggregation of PtIn intermetallic, ensuring excellent catalytic stability. These findings underscore the critical role of product molecules in shaping active site evolution at the atomic scale.
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http://dx.doi.org/10.1038/s41467-025-60153-1 | DOI Listing |
Nat Commun
June 2025
Hefei National Research Center for Physical Sciences at the Microscale, University of Science and Technology of China, Hefei, Anhui, P. R. China.
Understanding the dynamic evolution of heterogeneous catalysts is crucial yet challenging for elucidating the structure-performance relationships and enabling rational catalyst design. Herein, we reveal that PtIn alloy clusters gradually evolve into PtIn intermetallic in response to propylene, the product of propane dehydrogenation (PDH) reaction. Specifically, a PtIn/SiO catalyst has been fabricated, comprising sub-nanometric PtIn alloy clusters covered by an In overlayer, with In species locating at the metal-support interface.
View Article and Find Full Text PDFAdv Sci (Weinh)
March 2024
Department of Chemistry, Graduate School of Science, Kyoto University, Gokasho, Uji, Kyoto, 611-0011, Japan.
Materials that intrinsically exhibit localized surface plasmon resonance (LSPR) in the visible region have been predominantly researched on nanoparticles (NPs) composed of coinage metals, namely Au, Ag, and Cu. Here, as a coinage metal-free intermetallic NPs, colloidal PtIn NPs with a C1 (CaF -type) crystal structure are synthesized by the liquid phase method, which evidently exhibit LSPR at wavelengths similar to face-centered cubic (fcc)-Au NPs. Computational simulations pointed out differences in the electronic structure and photo-excited electron dynamics between C1-PtIn and fcc-Au NPs; reduces interband transition and stronger screening with smaller number of bound d-electrons compare with fcc-Au are unique origins of the visible plasmonic nature of C1-PtIn NPs.
View Article and Find Full Text PDFDalton Trans
August 2019
Inorganic Chemistry Department, Ivan Franko National University of Lviv, Kyryla and Mephodiya Street 6, 79005 Lviv, Ukraine.
The new intermetallic phase SrPtIn was synthesized by induction-melting of the elements in a sealed tantalum ampoule followed by long-term annealing for crystal growth. The SrPtIn structure was refined from single crystal X-ray diffraction data: Imma, a = 1674.7(6), b = 921.
View Article and Find Full Text PDFInorg Chem
December 2017
High Pressure and Synchrotron Radiation Physics Division, Bhabha Atomic Research Centre, Trombay, Mumbai 400085, India.
A study of the bonding and electronic properties of intermetallics under pressure is crucial in the design and development of novel materials for useful applications. These properties are largely controlled by the underlying crystal structures. Here we investigated the high-pressure structural behavior of PtIn using crystal structure search calculations, which efficiently combine evolutionary algorithms and state-of-the-art density functional theory.
View Article and Find Full Text PDFJ Am Chem Soc
March 2004
Department of Chemistry & Chemical Biology, Baker Laboratory, Cornell University, Ithaca, New York 14853-1301, USA.
The electrocatalytic activities of a wide range of ordered intermetallic phases toward a variety of potential fuels have been studied, and results have been compared to those of a pure polycrystalline platinum (Pt(pc)) electrode. A significant number of the ordered intermetallic phases exhibited enhanced electrocatalytic activity when compared to that of Pt, in terms of both oxidation onset potential and current density. The PtBi, PtIn, and PtPb ordered intermetallic phases appeared to be the most promising electrocatalysts tested thus far for fuel cell applications.
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