Alloy nanoparticles on oxide supports are widely used as heterogeneous catalysts in reactions involving oxygen. Here we discuss the oxidation behavior of Pd-Rh alloy nanoparticles on MgAl2O4(001) supports with a particle diameter from 6-11 nm. As an In situ tool, we employed high energy grazing incidence X-ray diffraction at a photon energy of 85 keV. We find that physical vapor deposited Pd-Rh nanoparticles grow epitaxially on MgAl2O4(001) with a truncated octahedral shape over the whole concentration range. During our systematic oxidation experiments performed at 670 K in the pressure range from 10(-3) to 0.1 mbar, we observe for Rh containing nanoparticles the formation of two different Rh oxide phases, namely RhO2 and a spinel-like Rh3O4 phase. PdO formation is only observed for pure Pd nanoparticles. This oxidation induced segregation behavior is also reflected in the oxidation induced enlargement of the average nanoparticle lattice parameter towards to value for pure Pd. Our results have ramifications for the phase separation behavior of alloy nanocatalysts under varying reducing and oxidizing environments.
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http://dx.doi.org/10.1039/c4cp01271b | DOI Listing |
Nanomaterials (Basel)
December 2024
Dipartimento di Chimica "Ugo Schiff", Università degli Studi di Firenze, Via della Lastruccia 3, 50019 Sesto Fiorentino, Italy.
In this study, we investigate the electrodeposition of various metals on silicon. Mn, Co, Ni, Ru, Pd, Rh, and Pt were identified as promising candidates for controlled electrodeposition onto silicon. Electrochemical evaluations employing cyclic voltammetry, Scanning Electron Microscopy (SEM) associated with energy-dispersive X-Ray Spectroscopy (SEM-EDS), and X-Ray Photoelectron Spectroscopy (XPS) techniques confirmed the deposition of Pd, Rh, and Pt as nanoparticles.
View Article and Find Full Text PDFAdv Mater
December 2024
Department of Chemical Engineering and SUNCAT Center for Interface Science and Catalysis, Stanford University, 443 via Ortega, Stanford, CA, 94305, USA.
Encapsulation of metal nanoparticles within oxide materials has been shown as an effective strategy to improve activity, selectivity, and stability in several catalytic applications. Several approaches have been proposed to encapsulate nanoparticles, such as forming core-shell structures, growing ordered structures (zeolites or metal-organic frameworks) on nanoparticles, or directly depositing support materials on nanoparticles. Here, a general nanocasting method is demonstrated that can produce diverse encapsulated metal@oxide structures with different compositions (Pt, Pd, Rh) and multiple types of oxides (AlO, AlO-CeO, ZrO, ZnZrO, InO, MnO, TiO) while controlling the size and dispersion of nanoparticles and the porous structure of the oxide.
View Article and Find Full Text PDFTalanta
August 2024
State Key Laboratory of Electroanalytical Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun, Jilin, 130022, PR China; School of Applied Chemistry and Engineering, University of Science and Technology of China, Hefei, Anhui, 230026, PR China. Electronic address:
The rapid development of nanozymes has offered substantial opportunities for the fields of biomedicine, chemical sensing, and food safety. Among these applications, multichannel sensors, with the capability of simultaneously detecting multiple target analytes, hold promise for the practical application of nanozymes in chemical sensing with high detection efficiency. In this study, Rh-decorated Pd nanocubes (Pd-Rh nanocubes) with significantly enhanced peroxidase-like activity are synthesized through the mediation of underpotential deposition (UPD) and subsequently employed to develop a multichannel colorimetric sensor for discriminating tea polyphenols (TPs) and tea authentication.
View Article and Find Full Text PDFMorphology-controlled nanoparticles of high entropy intermetallic compounds are quickly becoming high-value targets for catalysis. Their ordered structures with multiple distinct crystallographic sites, coupled with the "cocktail effect" that emerges from randomly mixing a large number of elements, yield catalytic active sites capable of achieving advanced catalytic functions. Despite this growing interest, little is known about the pathways by which high entropy intermetallic nanoparticles form and grow in solution.
View Article and Find Full Text PDFMolecules
July 2023
Institute of Chemical Technology and Engineering, Faculty of Chemical Technology, Poznan University of Technology, ul. Berdychowo 4, 60-965 Poznan, Poland.
This article presents studies on the precipitation of Pt, Pd, Rh, and Ru nanoparticles (NPs) from model and real multicomponent solutions using sodium borohydride, ascorbic acid, sodium formate, and formic acid as reducing agents and polyvinylpyrrolidone as a stabilizing agent. As was expected, apart from PGMs, non-precious metals were coprecipitated. The influence of the addition of non-precious metal ions into the feed solution on the precipitation yield and catalytic properties of the obtained precipitates was studied.
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