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Synthesis and Characterization of Silica Nanotubes with Radially Oriented Mesopores

Hierarchical silica nanotubes with radially oriented mesoporous channels perpendicular to the central axis of the tube were synthesized by using self‐assembled chiral anionic surfactant, co‐structure directing agent (CSDA) and silica precursor. The average inner diameter and the wall thickness were...

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Bibliographic Details
Published in:Advanced functional materials 2008-02, Vol.18 (4), p.541-550
Main Authors: Yu, Yatao, Qiu, Huibin, Wu, Xiaowei, Li, Huachun, Li, Yongsheng, Sakamoto, Yasuhiro, Inoue, Yoshihisa, Sakamoto, Kazutami, Terasaki, Osamu, Che, Shunai
Format: Article
Language:English
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Summary:Hierarchical silica nanotubes with radially oriented mesoporous channels perpendicular to the central axis of the tube were synthesized by using self‐assembled chiral anionic surfactant, co‐structure directing agent (CSDA) and silica precursor. The average inner diameter and the wall thickness were ∼94, ∼62, and ∼62 nm and to ∼27, ∼33, and ∼45 nm, respectively, by manipulating the synthesis gel composition, while the diameter of the wall mesopores was kept constant at ∼4 nm. These materials with such a unique structure were produced only with chiral surfactant and achiral or racemic surfactant did not give rise to mesoporous silica nanotubes. The existence of helicity in the lipid bilayer template was confirmed by means of circular dichroism spectroscopy. The mesoporous penetrating from outside to inside of silica nanotubes are thought to originate from the initial formation of self‐assembled lipid tubes with helical bilayers, which in turn re‐assemble to form the mesopores in the wall of the nanotubes upon addition of co‐structure directing agent and silica source. Hierarchical silica nanotubes with radially oriented mesoporous channels, with different average inner diameter, wall thickness and with a similar mesopore size of ∼4 nm were synthesized based on the re‐assembly of lipid nanotubes, co‐structure directing agent and inorganic silica precursor.
ISSN:1616-301X
1616-3028
1616-3028
DOI:10.1002/adfm.200700593