Issue 10, 2014

Mesoporous-structure-tailored hydrothermal synthesis and mechanism of the SrTiO3 mesoporous spheres by controlling the silicate semipermeable membranes with the KOH concentrations

Abstract

Mesoporous structure-tailored SrTiO3 mesoporous spheres have been hydrothermally realized by controlling the silicate semipermeable membranes with KOH concentration. The phase and microstructures were investigated by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, high-resolution transmission electron microscopy, thermogravimetric analysis and N2-physisorption techniques, respectively. Because the high KOH concentration lowers the polymerization degree of the silicate anion species, the silicate semipermeable membranes become thinner with increasing KOH concentration. Whereas the attenuated silicate semipermeable membranes favour the penetration of the metal ions, the primary SrTiO3 nanocrystallites for the self-assembly of the SrTiO3 mesoporous spheres grow larger as the KOH concentration increases. As a consequence, the mesoporous structures of the self-assembled SrTiO3 mesoporous spheres can be simply tailored by adjusting the KOH concentration of the hydrothermal reaction system. Moreover, because the attenuation of the silicate membrane facilitates the orientation attachment of the primary nanocrystallites, the self-assembled SrTiO3 mesoporous spheres trend to single-crystal-like with the increasing KOH concentration.

Graphical abstract: Mesoporous-structure-tailored hydrothermal synthesis and mechanism of the SrTiO3 mesoporous spheres by controlling the silicate semipermeable membranes with the KOH concentrations

Article information

Article type
Paper
Submitted
08 Sep 2013
Accepted
26 Nov 2013
First published
27 Nov 2013

CrystEngComm, 2014,16, 2025-2031

Mesoporous-structure-tailored hydrothermal synthesis and mechanism of the SrTiO3 mesoporous spheres by controlling the silicate semipermeable membranes with the KOH concentrations

G. Xu, S. Deng, Y. Zhang, X. Wei, X. Yang, Y. Liu, G. Shen and G. Han, CrystEngComm, 2014, 16, 2025 DOI: 10.1039/C3CE41809J

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