Imaging ice microstructures formed by water freezing with atomic resolution for the first time.

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

Tailored assemblies mimic natural enzyme activity with significantly higher stability.

In high-entropy oxides, chromium tends to segregate during growth due to oxidation-induced migration of smaller, high-valence cations.

Researchers at PNNL shared advances in artificial intelligence, cybersecurity, advanced imaging, and more at the Department of Homeland Security Research, Development, Test, and Evaluation Summit.

Researchers developed a way to precisely control dopant structures and locations in carbon-based materials.

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

Researchers developed a pathway for the solution synthesis of core–crown heterostructures with controlled electronic properties.

Under an optical field, nanoparticle attachment in a model system heavily depends on surface roughness.

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.

A team from PNNL contributed several articles to the Domestic Preparedness Journal showcasing recent efforts to explore the emergency management and artificial intelligence research and development landscape.

RemPlex and IAEA convene international leaders to tackle recruitment and retention in complex environmental cleanup efforts.

Chromium cations better adapt to changes in oxygen stoichiometry than iron cations.

Using interfacial charge transfer to control cation charges in oxide superlattices offers insights for designing functional heterostructures.

Calcium carbonate mineralization occurs through a multi-step process that begins with a dense liquid phase.

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

A newly funded project will develop the fundamental understanding of phenomena that underpin material properties important for quantum applications.

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.