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.

CO2 separation is key for natural gas purification, but conventional techniques are high-emission processes. New research reveals a novel, doubly segmented, CO2-selective membrane that increases CO2 permeability and reduces emissions.

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.

A multi-institutional team of researchers systematically compared extraction techniques for characterizing plant litter composition that relies on organic matter extraction.

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 new database allows researchers to connect lattice parameters and composition in olivine.

New methodology can evaluate the potential for carbon storage and critical mineral recovery in undercharacterized geological settings.

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

Research identifies the mechanisms through which peptoids affect ions in solution and a mineral surface, increasing the rate of carbonate crystal growth.

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.