LAUSR

HYPOTHESIS One of the main drawbacks of metal-supported materials, traditionally prepared by the impregnation of metal salts onto pre-synthesized porous supports, is the formation of large and unevenly dispersed particles. Generally, the larger are the particles, the lower is the number of catalytic sites. Maximum atom exposure can be reached within single-atom materials, which appear therefore as the next generation of porous catalysts. EXPERIMENTS Herein, we designed single iron atom-supported silica materials through sol-gel hydrothermal treatment using mixtures of a non-ionic surfactant (Pluronic P123) and a metallosurfactant (cetyltrimethylammoniumtrichloromonobromoferrate, CTAF) as porogens. The ratio between the Pluronic P123 and the CTAF enables to control the silica structural and textural properties. More importantly, CTAF acts as an iron source, which amount could be simply tuned by varying the non-ionic/metallo surfactants molar ratio. FINDINGS The fine distribution of iron atoms onto the silica mesopores results from the iron distribution within the mixed micelles, which serve as templates for the polymerization of the silica matrix. Several characterization methods were used to determine the structural and textural properties of the silica material (XRD, N2 sorption isotherms and TEM) and the homogeneous distribution and lack of clustering of iron atoms in the resulting materials (elemental analysis, magnetic measurements, pair distribution function (PDF), MAS-NMR and TEM mapping). The oxidation and spin state of single-iron atoms determined from their magnetic properties were confirmed by DFT calculations. This strategy might find straightforward applications in preparing versatile single atom catalysts, with improved efficiency compared to nanosized ones.