| Literature DB >> 31545533 |
Aisulu Aitbekova1, Emmett D Goodman1, Liheng Wu1,2, Alexey Boubnov2, Adam S Hoffman2, Arda Genc3, Huikai Cheng3, Lee Casalena3, Simon R Bare2, Matteo Cargnello1.
Abstract
Catalytic CO2 reduction to fuels and chemicals is a major pursuit in reducing greenhouse gas emissions. One approach utilizes the reverse water-gas shift reaction, followed by Fischer-Tropsch synthesis, and iron is a well-known candidate for this process. Some attempts have been made to modify and improve its reactivity, but resulted in limited success. Now, using ruthenium-iron oxide colloidal heterodimers, close contact between the two phases promotes the reduction of iron oxide via a proximal hydrogen spillover effect, leading to the formation of ruthenium-iron core-shell structures active for the reaction at significantly lower temperatures than in bare iron catalysts. Furthermore, by engineering the iron oxide shell thickness, a fourfold increase in hydrocarbon yield is achieved compared to the heterodimers. This work shows how rational design of colloidal heterostructures can result in materials with significantly improved catalytic performance in CO2 conversion processes.Entities:
Keywords: CO2 hydrogenation; hydrocarbons; hydrogen spillover; iron; ruthenium
Year: 2019 PMID: 31545533 DOI: 10.1002/anie.201910579
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336