Unlocking Low-Temperature Ammonia Decomposition via an Iron Metal-Organic Framework-Derived Catalyst Under Photo-Thermal Conditions.

Photo-thermal catalysis, leveraging both thermal and non-thermal solar contributions, emerges as a sustainable approach for fuel and chemical synthesis. In this study, an Fe-based catalyst derived from a metal-organic framework is presented for efficient photo-thermal ammonia (NH) decomposition. Optimal conditions, under light irradiation without external heating, result in a notable 55% NH conversion.

Highly Efficient and Stable Methane Dry Reforming Enabled by a Single-Site Cationic Ni Catalyst.

Zeolite-supported nickel (Ni) catalysts have been extensively studied for the dry reforming of methane (DRM). It is generally believed that prior to or during the reaction, Ni is reduced to a metallic state to act as the catalytic site. Here, we employed a ligand-protected synthesis method to achieve a high degree of Ni incorporation into the framework of the MFI zeolite.

Single-Site Molybdenum on Solid Support Materials for Catalytic Hydrogenation of N -into-NH.

Very stable in operando and low-loaded atomic molybdenum on solid-support materials have been prepared and tested to be catalytically active for N -into-NH hydrogenation. Ammonia synthesis is reported at atmospheric pressure and 400 °C with NH rates of approximately 1.3×10  μmol h  g using a well-defined Mo-hydride grafted on silica (SiO ).

Unearthing a Well-Defined Highly Active Bimetallic W/Ti Precatalyst Anchored on a Single Silica Surface for Metathesis of Propane.

Two compatible organometallic complexes, W(Me) (1) and TiNp (2), were successively anchored on a highly dehydroxylated single silica support (SiO) to synthesize the well-defined bimetallic precatalyst [(≡Si-O-)W(Me)(≡Si-O-)Ti(Np)] (4). Precatalyst 4 was characterized at the molecular level using advanced surface organometallic chemistry (SOMC) characterization techniques. The strong autocorrelation observed between methyl of W and Ti in H-H multiple-quantum NMR spectra demonstrates that W and Ti species are in close proximity to each other.

Immobilization of a molecular cobalt electrocatalyst by hydrophobic interaction with a hematite photoanode for highly stable oxygen evolution.

A unique modification of a hematite photoanode with perfluorinated Co-phthalocyanine (CoFPc) by strong binding associated with hydrophobic interaction is demonstrated. The resultant molecular electrocatalyst - a hematite photoanode hybrid material showed a significant onset shift and high stability for the photoelectrochemical oxidation evolution reaction (OER).