| Literature DB >> 30311342 |
Luis Miguel Azofra1, Natalia Morlanés1, Albert Poater2, Manoja K Samantaray1, Balamurugan Vidjayacoumar3, Khalid Albahily3, Luigi Cavallo1, Jean-Marie Basset1.
Abstract
Very stable in operando and low-loaded atomic molybdenum on solid-support materials have been prepared and tested to be catalytically active for N2 -into-NH3 hydrogenation. Ammonia synthesis is reported at atmospheric pressure and 400 °C with NH3 rates of approximately 1.3×103 μmol h-1 gMo -1 using a well-defined Mo-hydride grafted on silica (SiO2-700 ). DFT modelling on the reaction mechanism suggests that N2 spontaneously binds on monopodal [(≡Si-O-)MoH3 ]. Based on calculations, the fourth hydrogenation step involving the release of the first NH3 molecule represents the rate-limiting step of the whole reaction. The inclusion of cobalt co-catalyst and an alkali caesium additive impregnated on a mesoporous SBA-15 support increases the formation of NH3 with rates of circa 3.5×103 μmol h-1 gMo -1 under similar operating conditions and maximum yield of 29×103 μmol h-1 gMo -1 when the pressure is increased to 30 atm.Entities:
Keywords: N2 fixation; NH3 synthesis; heterogeneous catalysis; in silico design; molybdenum
Year: 2018 PMID: 30311342 DOI: 10.1002/anie.201810409
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336