Australia’s ARENA opens $70M hydrogen deployment funding round
Volkswagen to offer refreshed Tiguan with new plug-in hybrid powertrain in Europe

BNL, U Delaware team develops catalytic strategy for C-O bond activation; upgrading biomass to fuels and chemicals

Researchers at Brookhaven National Laboratory (BNL) and the University of Delaware have developed a catalytic strategy to promote the selective breaking of a carbon-oxygen bond—an essential step the conversion of lignocellulsoic biomass via hydrodeoxygenation to fuels and chemicals.

To demonstrate their principle, the team created a catalyst with highly dispersed Pt anchored onto TiO2 to convert furfuryl alcohol to 2-methylfuran, a potential biofuel. Their strategy—described in a paper published in Nature Catalysis—could be applied to design stable, active, and selective catalysts based on a wide range of metals supported on metal oxides to produce industrially useful chemicals and fuels from biomass-derived molecules.

Graphical-abstract-hr

The researchers loaded single atoms of platinum (yellow) on top of titania, a compound containing titanium (grey) and oxygen (red). This catalyst selectively breaks a bond between a carbon and oxygen in furfuryl alcohol, a five-member ring-shaped molecule with an attached side group (structure in black).


For a molecule to generate a particular product, the reaction has to be directed along a certain pathway because many side reactions that are not selective for the desired product are possible. To convert furfuryl alcohol into biofuel, the bond between carbon and oxygen atoms on the side group attached to the ring-shaped part of the molecule must be broken, without producing any reactions in the ring. Typically, the metal catalyst that breaks this bond also activates ring-related reactions. However, the catalyst designed in this study only breaks the side group carbon-oxygen bond.

—co-author Anibal Boscoboinik, BNL

Aromatic rings are structures with atoms connected through single or double bonds. In molecules derived from plant waste, aromatic rings often have oxygen-containing side groups. Transforming plant waste derivatives into useful products requires the removal of oxygen from these side groups by breaking specific carbon-oxygen bonds.

Biomass contains a lot of oxygen, which needs to be partially removed to leave behind more useful molecules for the production of renewable fuels, plastics, and high-performance lubricants. Hydrodeoxygenation, a reaction in which hydrogen is used as a reactant to remove oxygen from a molecule, is useful for converting biomass into value-added products.

—co-first author Jiayi Fu, a graduate student at the Catalysis Center for Energy Innovation (CCEI) at the University of Delaware (UD)

In this study, the scientists hypothesized that adding noble metals to the surfaces of moderately reducible metal oxides—those that can lose and gain oxygen atoms—would promote hydrodeoxygenation.

Removing oxygen from the oxide surface forms an anchoring site where molecules can be held in place so the necessary bonds can be broken and formed. Previous studies in the catalysis and semiconductor communities have shown how much impurities can influence the surface.

—co-first author and UD CCEI graduate student Jonathan Lym

To test their hypothesis, the team selected platinum as the noble metal and titanium dioxide (titania) as the metal oxide. Theoretical calculations and modeling indicated that the formation of oxygen vacancies is more energetically favorable when single atoms of platinum are introduced onto the surface of titania.

After synthesizing the platinum-titania catalyst at UD, they performed various structural and chemical characterization studies using facilities at Brookhaven and Argonne National Labs. At the CFN Electron Microscopy Facility, they imaged the catalyst at high resolution with a scanning transmission electron microscope. At Brookhaven’s National Synchrotron Light Source II (NSLS-II), they used the In situ and Operando Soft X-ray Spectroscopy (IOS) beamline and the Quick X-ray Absorption and Scattering (QAS) beamline to track the chemical (oxidation) state of platinum. Through complementary x-ray spectroscopy studies at Argonne’s Advanced Photon Source (APS), they determined the distance between atoms in the catalyst.

Back at Delaware, the team performed reactivity studies in which they put the catalyst and furfuryl alcohol in a reactor and detected the products through gas chromatography. In addition to these experiments, they theoretically calculated the amount of energy required for different steps of the reaction to proceed. On the basis of these calculations, they ran computer simulations to determine the preferable reaction pathways. The simulated and experimental product distributions both indicated that negligible ring-reaction products are generated when a low concentration of platinum is present. As this concentration is increased, the platinum atoms begin to aggregate into larger clusters that incite ring reactions.

The complementary experimental and computational framework allows for a detailed understanding of what is happening on the surface of a very complex material in a way that we can generalize concepts for the rational design of catalysts. These concepts can help in predicting suitable combinations of metals and metal oxides to carry out desired reactions for converting other molecules into valuable products.

—Anibal Boscoboinik

Resources

  • Fu, J., Lym, J., Zheng, W. et al. (2020) “C–O bond activation using ultralow loading of noble metal catalysts on moderately reducible oxides.” Nat Catal doi: 10.1038/s41929-020-0445-x

Comments

The comments to this entry are closed.