An ordered mesoporous organosilica hybrid material with a crystal-like wall structure

被引:1190
作者
Inagaki, S [1 ]
Guan, S
Ohsuna, T
Terasaki, O
机构
[1] Toyota Cent Res & Dev Labs Inc, Aichi 4801192, Japan
[2] Tohoku Univ, Mat Res Inst, Sendai, Miyagi 9808577, Japan
[3] Tohoku Univ, Grad Sch Sci, JST, CREST, Sendai, Miyagi 9808578, Japan
[4] Tohoku Univ, Dept Phys, Sendai, Miyagi 9808578, Japan
关键词
D O I
10.1038/416304a
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Surfactant-mediated synthesis strategies are widely used to fabricate ordered mesoporous solids(1-6) in the form of metal oxides(7), metals(8), carbon(9) and hybrid organosilicas(10-14). These materials have amorphous pore walls, which could limit their practical utility. In the case of mesoporous metal oxides, efforts to crystallize the framework structure by thermal(15,16) and hydrothermal treatments(17) have resulted in crystallization of only a fraction of the pore walls. Here we report the surfactant-mediated synthesis of an ordered benzene-silica hybrid material; this material has an hexagonal array of mesopores with a lattice constant of 52.5 Angstrom, and crystal-like pore walls that exhibit structural periodicity with a spacing of 7.6 Angstrom along the channel direction. The periodic pore surface structure results from alternating hydrophilic and hydrophobic layers, composed of silica and benzene, respectively. We believe that this material is formed as a result of structure-directing interactions between the benzene-silica precursor molecules, and between the precursor molecules and the surfactants. We expect that other organosilicas and organo-metal oxides can be produced in a similar fashion, to yield a range of hierarchically ordered mesoporous solids with molecular-scale pore surface periodicity.
引用
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页码:304 / 307
页数:4
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