Incorporation of Silicon and Manganese into Mesoporous Aluminophosphate Thin Film with Cubic Pore Arrangement

S. CECOWSKI; N. NOVAK TUSAR; M. RANGUS; G. MALI; G. J. A. A. SOLER ILLIA; V. KAUCIC

MICROPOROUS AND MESOPOROUS MATERIALS

ELSEVIER SCIENCE BV

Año: 2010 vol. 135 p. 161 - 169

1387-1811

Mesoporous aluminophosphate thin films and xerogels with ordered three-dimensional pore arrangement, modified by silicon or silicon and manganese, were synthesized. Aluminophosphate reaction mixtures were templated with non ionic polymer surfactant Pluronic F127 and deposited as thin layers of precursor solution on Petri dishes for xerogels and on glass substrates for thin films. Surfactant removal was investigated by thermal analysis. Small Angle X-ray Scattering measurements showed that calcined silicoaluminophosphate (SAPO) and manganese silicoaluminophosphate (MnSAPO) thin films have highly ordered mesostructures, which remain stable up to at least 400ºC. The mesostructures exhibit cubic symmetry described by an Im3m space group. Cubic mesostructure was confirmed also by TEM, SEM and AFM microscopy. Incorporation of silicon and manganese into the aluminophosphate framework was studied by solid-state NMR and X-ray absorption spectroscopy. Silicon-rich domainswere detected in calcined SAPO and MnSAPO xerogels and in MnSAPO thin films. The observation of Si(OSi)3(OAl) framework units at the border of such domains suggests that acid sites might be included within silicoaluminophosphate walls. Mn3+ and Mn2+ cations are present in the MnSAPO frameworks of calcined xerogels and thin films in the molar ratio of 40%/60%. Manganese cations are coordinated to four oxygen atoms, suggesting that they are incorporated within the framework and that they can act as framework redox sites.