The Best of Both Catalytic Worlds

Catalysts are substances that speed up the rates of chemical reactions without themselves being chemically changed. Industrial catalysts come in two main types – heterogeneous, in which the catalyst is in a different phase from the reactants; and homogeneous, in which catalyst and the reactants are in the same phase. Heterogeneous catalysts are valued for their sustainability because they can be recycled. Homogeneous catalysts are valued for their product selectivity as their properties can be easily tuned through relatively simple chemistry.

Researchers with the U.S. Department of Energy (DOE)’s Lawrence Berkeley National Laboratory (Berkeley Lab) have combined the best properties of both types of industrial catalysts by encapsulating nanoclusters of a metallic heterogeneous catalyst within the branched arms of the molecules known as dendrimers.

The results are heterogenized homogeneous nanocatalysts that are sustainable and feature high reactivity and selectivity. Furthermore, these heterogenized homogeneous nanocrystals hold promise for bridging the gap between industrial catalysts, which carry out simple reactions, and a third type of catalyst, the proteins known as enzymes, that nature uses to carry out the complex reactions of biochemistry.

“Using cyclopropanation reactions catalyzed by dendrimer-encapsulated gold and other metal nanoclusters, including platinum, palladium and rhodium, we have demonstrated that changing the dendrimer properties allows catalytic reactivity in a heterogeneous catalyst to be tuned in a similar fashion to ligand modification in a homogeneous catalyst,” says world renowned catalysis chemist Gabor Somorjai, one of the leaders of this research. “Furthermore, we have shown that these heterogeneous catalysts employed in a fixed-bed flow reactor allow fine control over the residence time of the reactants and thus enable control over product distribution in a way that is not easily available for homogeneous catalysts.”

Somorjai is a senior scientist with Berkeley Lab’s Materials Sciences Division, where he directs the Surface Science and Catalysis Program, and a professor of chemistry with the Chemistry Department at the University of California Berkeley. He is the corresponding author along with chemist Dean Toste, who also holds joint appointments with Berkeley Lab and UC Berkeley, of a paper describing this research in the journal Nature Chemistry. The paper is titled “Control of selectivity in heterogeneous catalysis by tuning nanoparticle properties and reactor residence time.” Other authors were Elad Gross and Jack Hung-Chang Liu.

Catalysts are used to initiate virtually every industrial manufacturing process that involves chemistry. Metal catalysts have been the traditional workhorses, but in recent years nano-sized catalysts have surged in importance.

“From our work, it has become increasingly clear that at the molecular level, all catalysts – heterogeneous, homogeneous and enzymes – function the same,” Somorjai says. “We have now proven that working with metal nanoclusters, the same chemistry can be done with heterogeneous or homogeneous catalysts.”

Adds corresponding author Dean Toste, “It’s an exciting prospect that there may be universal design principles that can be applied to constructing 100-percent selective catalysts, whether they are homogeneous or heterogeneous. Ultimately, if these principles can be uncovered, it should be possible to design complex networks of selective catalysts that generate products with high efficiency.”

The key to the success of this latest research was the encapsulation of metal nanoparticles inside dendrimers. The term “dendrimer” comes from the Greek word for “tree,” an apt description for branching polymer molecules that resemble a worm’s eye view of a tree’s root system. Somorjai, Toste and their co-authors used gold nanoclusters and polyamidoamine (PAMAM), a common class of dendrimers suitable for numerous applications in materials and biotechnology. They successfully tested their dendrimer-encapsulated catalyst on cyclopropane, a biomolecule widely used in the pharmaceutical and chemical industries, and typically formed through homogeneous catalysis.

“By designing the molecular architecture of our catalyst to feature a highly crowded matrix, we greatly enhanced the product selectivity of our reaction, similar to the use of bulky ligands in a homogeneous catalyst,” says Elad Gross, the lead author of the Nature Chemistry paper and a member of Somorjai’s research group. “Product selectivity was further enhanced by employing the catalyst in a flow reactor and changing the flow rate of the reactants. This gave us a high degree of control over our secondary reactions, again similar to the role that ligand electronic properties play in tuning the chemical selectivity of homogeneous catalysts.”

Given that flow systems are widely used in industrial chemistry, the concept of replacing homogeneous catalysts with dendrimer-encapsulated heterogeneous catalysts whose product selectivity can be controlled should be a popular alternative. For example, the catalysis of cyclopropane could be tuned to favor the formation of cyclopropanes that are critical components of cancer and cholesterol medicines. The recyclability of these dendrimer-encapsulated heterogeneous catalysts is another major advantage.

“Highly selective catalysts, especially those that can be recycled readily, are vital for the development of sustainable chemical processes,” Gross says. “In the future, with our technique it should be possible to combine heterogeneous and homogeneous catalysts to get specific products with very high selectivity.”

This research was supported by the DOE Office of Science.