Switching a pendant nitrogen to phosphorous leads to an accelerated rate of carbon dioxide hydrogenation to methanol.

Ketene generated from surface acetate can desorb, migrate through interparticle voids, and react on titanium dioxide nanoparticles to form acetone.

Titanium dioxide surface structure exhibits water inhibition by forming distinct water–alkanol complexes.

Yong Wang’s joint appointment connects PNNL, WSU, and the next generation of scientists.

Demonstrated that cathodic potential accelerates aqueous phase benzaldehyde hydrogenation.

Global exercise advances nuclear forensic science and investigative capabilities.

PNNL experts trained Armenian engineers in ultrasonic testing, advancing local expertise for nuclear power plant inspections.

Research provided definitive spectroscopic characterization, reactivity, and deactivation of a reactive monomeric diphosphine-copper hydride intermediate.

Developed a method for selectively anchoring diverse divalent metal cations in zeolites, important for precise control over catalytic materials.

Developed a simple kinetic framework for evaluating catalyst hydride transfer ability.

PNNL has formed a partnership with the Orlando-based firm Refinity, which has licensed a key process from PNNL that will help the company convert mixed plastic waste into valuable industrial products like chemicals, plastics, and fuels.

A low-temperature, single-stage catalytic process converts PVC and polyolefin into valuable alkanes.

A comprehensive investigation provides quantitative data on the interaction between zeolite pores and linear alcohols, with hydroxyl group interactions playing the largest role.

After isolating copper hydride monomers, researchers identified the mechanistic details of catalyst aggregation and cluster formation.

The low-temperature breakdown of polyolefins is driven by carbenium ions generated from chloroaluminate ionic liquids.

PNNL chemical engineer Mariefel Olarte shares passion for mentoring students and the next-generation workforce.

Tuning the environment of supported palladium atoms with hydrogen treatment enhances their catalytic activity.

A switchable single-atom catalyst is activated in the presence of surface intermediates and reverts to its stable inactive form when the reaction is completed.

Increasing the concentration of ions in zeolite micropores leads to a significant increase in the rate of acid catalyzed reactions.

Electronic modifications from hydrogen spillover onto the oxide support increase the activity of single-atom rhodium catalysts.