Stepwise assembly of the active site of [NiFe]-hydrogenase
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The selective incorporation of isolated framework Lewis acid sites in specific crystallographic positions in high-silica zeolites was achieved successfully by applying a rationalized post-synthetic grafting methodology.
The reactivity and reaction mechanism of a Pt single atom supported on ceria can be tuned by changing its local electronic and atomic structure through Gd doping.
A structural and functional biomimetic Ni( ii )N 3 O complex, capable of O 2 mediated dioxygenase like C–C bond cleavage, via a putative high-valent Ni intermediate.
Neutron crystallography revealed protonation states in Tth SHMT-FA complex. Glu53 is protonated but other residues maintain protonation states upon FA binding. Structural analyses support key roles of Glu53 and gating loop dynamics in SHMT function.
Completely or partially ordered intermetallic compounds possess unique geometric ensembles, electronic structure and chemical bonding scenarios, establishing them as an emergent class of catalytic materials for selective hydrogenation reactions.
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Adopting low-index single-crystal surfaces as models for metal nanoparticle catalysts has been questioned by the experimental findings of adsorbate-induced formation of subnanometer clusters on several single-crystal surfaces. Here we used density functional theory calculations to elucidate the conditions that lead to cluster formation and show how adatom formation energies enable efficient screening of the conditions required for adsorbate-induced cluster formation. We studied a combination of eight face-centered cubic transition metals and 18 common surface intermediates and identified systems relevant to catalytic reactions, such as carbon monoxide (CO) oxidation and ammonia (NH 3 ) oxidation. We used kinetic Monte Carlo simulations to elucidate the CO-induced cluster formation process on a copper surface. Scanning tunneling microscopy of CO on a nickel (111) surface that contains steps and dislocations points to the structure sensitivity of this phenomenon. Metal-metal bond breaking that leads to the evolution of catalyst structures under realistic reaction conditions occurs much more broadly than previously thought.
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The goals of this project are to design and develop tailored dual-functional materials (DFMs) and the accompanying pressure-swing process for the reactive capture and conversion (RCC) of CO 2 to methanol, a vital product in the chemical market and a versatile precursor to fuels. Throughout this project, NREL researcher team has successfully developed 2 groups of DFM and associated cyclic RCC procedure to selectivity produce either methanol or CO, which is a major intermediate for methanol synthesis with commercially available technologies.
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