A general synthesis approach for supported bimetallic nanoparticles via surface inorganometallic chemistry

Author:

Ding Kunlun1ORCID,Cullen David A.2ORCID,Zhang Laibao1ORCID,Cao Zhi34ORCID,Roy Amitava D.5ORCID,Ivanov Ilia N.6ORCID,Cao Dongmei7ORCID

Affiliation:

1. Department of Chemical Engineering, Louisiana State University, Baton Rouge, LA 70803, USA.

2. Materials Science and Technology Division, Oak Ridge National Laboratory, Oak Ridge, TN 37831, USA.

3. State Key Laboratory of Coal Conversion, Institute of Coal Chemistry, Chinese Academy of Sciences, Taiyuan, Shanxi 030001, People’s Republic of China.

4. Synfuels China Co., Ltd., Beijing 100195, People’s Republic of China.

5. Center for Advanced Microstructures and Devices, Louisiana State University, Baton Rouge, LA 70806, USA.

6. Center for Nanophase Materials Sciences, Oak Ridge National Laboratory, Oak Ridge, TN 37831, USA.

7. Shared Instrumentation Facility, Louisiana State University, Baton Rouge, LA 70803, USA.

Abstract

More alloying on silica Controlling the stoichiometry and achieving a high degree of alloying of metals at ultrasmall scales for catalysis can be difficult. Double complex salts, formed by a cation like Pd(NH 3 ) 4 2+ and an anion like IrCl 6 2− , should be excellent precursors but are poorly soluble and difficult to adsorb directly on metal oxide surfaces. Ding et al. show that sequentially adsorbing the cations and anions from organic solvents onto a silica surface, followed by heating in hydrogen, creates well-mixed nanoparticles, most less than 3 nanometers in diameter, for a variety of alloys. These materials were then tested as catalysts for acetylene hydrogenation to ethylene. Science , this issue p. 560

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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