TY - JOUR
T1 - Stability of Colloidal Iron Oxide Nanoparticles on Titania and Silica Support
AU - Krans, Nynke A.
AU - Van Uunen, Dónal L.
AU - Versluis, Caroline
AU - Dugulan, Achim Iulian
AU - Chai, Jiachun
AU - Hofmann, Jan P.
AU - Hensen, Emiel J.M.
AU - Zečević, Jovana
AU - De Jong, Krijn P.
PY - 2020
Y1 - 2020
N2 - Using model catalysts with well-defined particle sizes and morphologies to elucidate questions regarding catalytic activity and stability has gained more interest, particularly utilizing colloidally prepared metal(oxide) particles. Here, colloidally synthesized iron oxide nanoparticles (FexOy-NPs, size ∼7 nm) on either a titania (FexOy/TiO2) or a silica (FexOy/SiO2) support were studied. These model catalyst systems showed excellent activity in the Fischer-Tropsch to olefin (FTO) reaction at high pressure. However, the FexOy/TiO2 catalyst deactivated more than the FexOy/SiO2 catalyst. After analyzing the used catalysts, it was evident that the FexOy-NP on titania had grown to 48 nm, while the FexOy-NP on silica was still 7 nm in size. STEM-EDX revealed that the growth of FexOy/TiO2 originated mainly from the hydrogen reduction step and only to a limited extent from catalysis. Quantitative STEM-EDX measurements indicated that at a reduction temperature of 350 °C, 80% of the initial iron had dispersed over and into the titania as iron species below imaging resolution. The Fe/Ti surface atomic ratios from XPS measurements indicated that the iron particles first spread over the support after a reduction temperature of 300 °C followed by iron oxide particle growth at 350 °C. Mössbauer spectroscopy showed that 70% of iron was present as Fe2+, specifically as amorphous iron titanates (FeTiO3), after reduction at 350 °C. The growth of iron nanoparticles on titania is hypothesized as an Ostwald ripening process where Fe2+ species diffuse over and through the titania support. Presynthesized nanoparticles on SiO2 displayed structural stability, as only ∼10% iron silicates were formed and particles kept the same size during in situ reduction, carburization, and FTO catalysis.
AB - Using model catalysts with well-defined particle sizes and morphologies to elucidate questions regarding catalytic activity and stability has gained more interest, particularly utilizing colloidally prepared metal(oxide) particles. Here, colloidally synthesized iron oxide nanoparticles (FexOy-NPs, size ∼7 nm) on either a titania (FexOy/TiO2) or a silica (FexOy/SiO2) support were studied. These model catalyst systems showed excellent activity in the Fischer-Tropsch to olefin (FTO) reaction at high pressure. However, the FexOy/TiO2 catalyst deactivated more than the FexOy/SiO2 catalyst. After analyzing the used catalysts, it was evident that the FexOy-NP on titania had grown to 48 nm, while the FexOy-NP on silica was still 7 nm in size. STEM-EDX revealed that the growth of FexOy/TiO2 originated mainly from the hydrogen reduction step and only to a limited extent from catalysis. Quantitative STEM-EDX measurements indicated that at a reduction temperature of 350 °C, 80% of the initial iron had dispersed over and into the titania as iron species below imaging resolution. The Fe/Ti surface atomic ratios from XPS measurements indicated that the iron particles first spread over the support after a reduction temperature of 300 °C followed by iron oxide particle growth at 350 °C. Mössbauer spectroscopy showed that 70% of iron was present as Fe2+, specifically as amorphous iron titanates (FeTiO3), after reduction at 350 °C. The growth of iron nanoparticles on titania is hypothesized as an Ostwald ripening process where Fe2+ species diffuse over and through the titania support. Presynthesized nanoparticles on SiO2 displayed structural stability, as only ∼10% iron silicates were formed and particles kept the same size during in situ reduction, carburization, and FTO catalysis.
UR - http://www.scopus.com/inward/record.url?scp=85087588482&partnerID=8YFLogxK
U2 - 10.1021/acs.chemmater.0c01352
DO - 10.1021/acs.chemmater.0c01352
M3 - Article
AN - SCOPUS:85087588482
SN - 0897-4756
VL - 32
SP - 5226
EP - 5235
JO - Chemistry of Materials
JF - Chemistry of Materials
IS - 12
ER -