TY - JOUR
T1 - Mixed silica titania materials prepared from a single-source sol-gel precursor: A time-resolved SAXS study of the gelation, aging, supercritical drying, and calcination processes
AU - Torma, Viktoria
AU - Peterlik, Herwig
AU - Bauer, Ulrike
AU - Rupp, Wolfgang
AU - Hüsing, Nicola
AU - Bernstorff, Sigrid
AU - Steinhart, Milos
AU - Goerigk, Günter
AU - Schubert, Ulrich
N1 - DOI: 10.1021/cm047996n
Coden: CMATE
Affiliations: Institute of Materials Chemistry, Vienna University of Technology, Getreidemarkt 9, A-1060 Wien, Austria; Institute of Materials Physics, University of Vienna, Boltzmanngasse 5, A-1090 Wien, Austria; Sincrotrone Trieste S.C.p.A, Strada Statale 14, I-34012 Trieste, Italy; Institut für Festkörperforschung, Forschungszentrum Jülich, D-52425 Jülich, Germany
Adressen: Schubert, U.; Institute of Materials Chemistry; Vienna University of Technology; Getreidemarkt 9 A-1060 Wien, Austria; email: [email protected]
Import aus Scopus: 2-s2.0-20744436846
17.12.2007: Datenanforderung 2031 (Import Sachbearbeiter)
PY - 2005
Y1 - 2005
N2 - The morphology of gels prepared from a silica/titania single-source precursor (1), obtained by reaction of 3-oxoethyl-6-trimethoxysilyl-hexan-2-one with Ti(OiPr)4, was investigated by small-angle X-ray scattering (SAXS) through all stages of the preparation process, that is, gelation, aging, drying, and calcination. The same investigations were performed for mixtures of 1 and Si(OEt)4. Immediately after the start of the reaction small primary particles are formed, the size of which (r = 0.5 ‘ 0.1 nm) remains constant through the gelation and aging process. Anomalous small-angle X-ray scattering (ASAXS) measurements strongly indicate that the primary particles are formed by hydrolysis and condensation of the titanium alkoxide moiety of 1. Condensation proceeds by a slower aggregation of the primary particles. Additional Si/O from Si(OEt)4 is incorporated between the clusters. The size of the mass fractal secondary particles formed by aggregation of the primary particles increases approximately exponentially with the time. Drying by either solvent evaporation or supercritical extraction with CO2 results in a decrease of the primary particle size to r = 0.4 nm, and the secondary particles also become smaller. The primary particles disappear during calcination in air, that is, when the organic groups tethering the silicon and titanium atoms are destroyed. However, the general structure of the network is maintained. Œ 2005 American Chemical Society.
AB - The morphology of gels prepared from a silica/titania single-source precursor (1), obtained by reaction of 3-oxoethyl-6-trimethoxysilyl-hexan-2-one with Ti(OiPr)4, was investigated by small-angle X-ray scattering (SAXS) through all stages of the preparation process, that is, gelation, aging, drying, and calcination. The same investigations were performed for mixtures of 1 and Si(OEt)4. Immediately after the start of the reaction small primary particles are formed, the size of which (r = 0.5 ‘ 0.1 nm) remains constant through the gelation and aging process. Anomalous small-angle X-ray scattering (ASAXS) measurements strongly indicate that the primary particles are formed by hydrolysis and condensation of the titanium alkoxide moiety of 1. Condensation proceeds by a slower aggregation of the primary particles. Additional Si/O from Si(OEt)4 is incorporated between the clusters. The size of the mass fractal secondary particles formed by aggregation of the primary particles increases approximately exponentially with the time. Drying by either solvent evaporation or supercritical extraction with CO2 results in a decrease of the primary particle size to r = 0.4 nm, and the secondary particles also become smaller. The primary particles disappear during calcination in air, that is, when the organic groups tethering the silicon and titanium atoms are destroyed. However, the general structure of the network is maintained. Œ 2005 American Chemical Society.
U2 - 10.1021/cm047996n
DO - 10.1021/cm047996n
M3 - Article
SN - 0897-4756
VL - 17
SP - 3146
EP - 3153
JO - Chemistry of Materials
JF - Chemistry of Materials
IS - 12
ER -