Abstract

One of the key factors for producing highly dispersed controlled nanoparticles is the method used for metal deposition. The decomposition of metal-organic precursors is a good method for deposition of metal nanoparticles with very small sizes and narrow size distributions on the surface of various supports. The preparation process of Pd and bimetallic Pd-Sn nanoparticles supported onto γ-Al2O3 is considered. The samples were prepared by diffusional co-impregnation of the γ-Al2O3 support by using organometallic Pd(acac)2 and Sn(acac)2Cl2 precursors. To achieve the formation of Pd and bimetallic Pd-Sn nanoparticles on the support surface, the synthesized samples were then subjected to thermal decomposition under Ar (to decompose the organometallic bound to the surface while keeping the formed nanoparticles small) followed by an oxidation in O2 (to eliminate the organic compounds remaining on the surface) and a reduction in H2 (to reduce the nanoparticles oxidized during the previous step). A combination of methods (ICP-OES, TPR-H2, XPS, TEM/EDX) was used to compare the physical-chemical properties of the synthesized Pd and bimetallic Pd-Sn nanoparticles supported on the γ-Al2O3. The three samples exhibit narrow size distribution with a majority on nanoparticles between 3 and 5 nm. Local EDX measurements clearly showed that the nanoparticles are bimetallic with the expected chemical composition and the measured global composition by ICP-OES. The surface composition and electronic properties of Pd and Sn on the γ-Al2O3 support were investigated by XPS, in particular the chemical state of palladium and tin after each step of thermal decomposition treatments (oxidation, reduction) by the XPS method has been carried out. The reducibility of the prepared bimetallic nanoparticles was measured by hydrogen temperature programmed reduction (TPR-H2). The temperature programmed reduction TPR-H2 experiments have confirmed the existence of strong surface interactions between Pd and Sn, as evidenced by hydrogen spillover of Pd to Sn (Pd-assisted reduction of oxygen precovered Sn). These results lead us to propose a mechanism for the formation of the bimetallic nanoparticles.

Highlights

  • The Transmission electron microscopy (TEM)-energy dispersive X-ray (EDX) study confirms that co-impregnation is an efficient and simple method to produce bimetallic

  • Morphology analysis of obtained samples by TEM showed for both Pd and bimetallic Pd-Sn samples that the supported nanoparticles have a small size with rather narrow uniform size distribution over the support surface

  • The results shown for both bimetallic Pd-Sn sample clearly reveal that these individual nanoparticles are bimetallic and establish the validity of the local EDX measurements performed over small collections of nanoparticles

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Summary

Introduction

In the field of catalysis [13,15], the addition of a second metal to an already active metal may improve its catalytic performance increasing its activity and/or selectivity allowing allowing to work at lower temperatures and to form as a small amount as possible of unwanted products. Formation of a bimetallic may give the possibility of modulating the activity ( a very active phase may lead to strong deactivation) and the selectivity being able to change the orientation of the products of a selective reaction following the needs. It can provide better stability of the active phase and better resistance to poisoning. If we add to the previous points the possibility of diluting the active sites of, often, expensive metals with low-cost metals we have a set of factors that will lead to lower costs of operation and materials

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