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.

PNNL recently hosted a training exercise that immersed the U.S. Coast Guard 2013 Cyber Protection Team in a lifelike simulation of a cyberattack on a U.S. port terminal.

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

CESER and PNNL convened a three-day summit with more than 100 state officials, cybersecurity experts, and industry leaders across 35 states to advance energy security planning, cyber risk assessment, and fortify protections against attacks.

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.

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

The Testing Risks of AI for National Security Taskforce will address critical safety and security concerns related to artificial intelligence.

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.

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

ChemReasoner combines decades of chemistry knowledge with large language models to propose strategies for effective new catalysts.

Fully identifying what controls nanocrystal assembly requires incorporating non-traditional forces into models.