New research finds that reaction rates for cyclic alcohol dehydration increase as ionic strength increases, independent of reaction mechanism.

Theoretical work shows that an important natural iron source can be described as a nanoscale composite of different, but experimentally indistinguishable, structures.

IDREAM study characterizes chemical species and mechanisms that control aluminum salt and mineral crystallization for nuclear waste retrieval, processing.

New study elucidates the complex relaxation kinetics of supercooled water using a pulsed laser heating technique at previously inaccessible temperatures.

Local ionic strength within zeolite pores tailors the chemical potential of reacting molecules, leading to high cyclohexanol dehydration activity

Spectroscopic experiments reveal significant variations in the electronic structures of actinide tetrafluorides despite their nearly identical crystal structures.

Tetranuclear molybdenum sulfide clusters encaged in zeolites mimic the FeMo-cofactor of nitrogenase, offering a new opportunity for improving industrial hydrotreatment processes.

New research uncovers the mechanism of carbon dioxide reduction by metal-O-Fe bonds of single-metal atoms and metal nanoparticles supported by oxidic surfaces.

Researchers gained insight into the interfacial radiation chemistry of radioactive waste sludge through studies of surface functional groups on model aluminum-containing solids

IDREAM researchers have discovered the chemical processes that underpin gibbsite solubility in sodium hydroxide, including sodium nitrate and sodium nitrite interactions.

A new study connects microscopic molecular-level descriptions with properties of a liquid at the macroscopic scale.

Combining transition state theory with Marcus theory provides insight into the fundamental processes of proton transfer in water.

Characterizing the electron redistribution that allows the binding of molecular nitrogen to the catalytic core of nitrogenase.

A new approach uses CO₂ to favorably co-produce methanol and glycols in a simple one-pot reaction.

PNNL researchers have developed a new class of chemistry focused on carbon capture technology and made incremental strides in driving down costs.

The structure-directing agent directly interacts with framework components during material formation.

A nanosized metal catalyst directly bonded to a metal-organic framework is active in converting carbon dioxide to methanol.

Artificial structuring in carefully designed (SrNiO3)1/(LaFeO3)n superlattices stabilized Ni4+ cations that would otherwise be unstable

Contributions from researchers across Pacific Northwest National Laboratory (PNNL) were recently recognized in the preliminary findings of a Secretary of Energy Advisory Board (SEAB) report.

This research addresses two topics that are not well understood in literature: the interplay between organic linkers and substrates during MOF crystallization, as well as the mechanisms that control heterostructure formation in solutions.