AVS 59th Annual International Symposium and Exhibition
    Oxide Heterostructures-Interface Form & Function Focus Topic Monday Sessions
       Session OX+SS+TF+MI-MoA

Invited Paper OX+SS+TF+MI-MoA3
Catalyst Synthesis by Atomic Layer Deposition

Monday, October 29, 2012, 2:40 pm, Room 007

Session: Chemistry of Oxide Surfaces and Interfaces
Presenter: P.C. Stair, Northwestern University & Argonne National Laboratory
Correspondent: Click to Email

Atomic Layer Deposition (ALD) has enormous potential for the synthesis of advanced heterogeneous catalysts with control of composition and structure at the atomic scale. The ability of ALD to produce conformal oxide coatings on porous, high-surface area materials can provide completely new types of catalyst supports. At the same time ALD can achieve highly uniform catalytically active metal and oxide phases with (sub-) nanometer dimensions.

Vanadium oxide species supported on high surface area oxides are among the most important catalytic materials for the selective, oxidative conversion of hydrocarbons to useful chemicals. In our laboratory ALD has been used to synthesize both the catalytic vanadium oxide and the supporting oxide on both high surface powders and anodic aluminum oxide (AAO) nanoliths. These materials have been characterized by SEM, XRF, ICP, UV-Vis absorption spectroscopy, Raman spectroscopy and evaluated for the oxidative dehydrogenation (ODH) of cyclohexane.

More recently we have studied the synthesis of supported metal particles and developed what we call “ABC-type” ALD in which metal nanoparticles and support materials are grown sequentially in each ALD cycle. This method makes possible the synthesis exceptionally small particles, ca. 0.5 nm. Using additional ALD support layers at the conclusion of the growth, the metal particles can be stabilized against sintering while still remaining active at high temperatures and reaction conditions. Moreover, the catalysts resist coke formation which is a leading cause of catalyst deactivation. These properties are imparted as a result of anchoring step and edge atom sites while leaving facet sites open for catalysis.