Synthesis of ordered mesoporous Fe3O4 and γ-Fe2O3 with crystalline walls using post-template reduction/oxidation

被引:311
作者
Jiao, Feng
Jumas, Jean-Claude
Womes, Manfred
Chadwick, Alan V.
Harrison, Andrew
Bruce, Peter G. [1 ]
机构
[1] Univ St Andrews, Sch Chem, St Andrews KY16 9ST, Fife, Scotland
[2] Univ St Andrews, EaStChem, St Andrews KY16 9ST, Fife, Scotland
[3] Univ Montpellier 2, Lab Agregats Mol & Mat Inorgan, UMR 5072, F-34095 Montpellier 5, France
[4] Univ Kent, Sch Phys Sci, Ctr Mat Res, Canterbury CT2 7NR, Kent, England
[5] Univ Edinburgh, Sch Chem, Edinburgh EH9 3JJ, Midlothian, Scotland
[6] Univ Edinburgh, EaStChem, Edinburgh EH9 3JJ, Midlothian, Scotland
关键词
D O I
10.1021/ja063662i
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Ordered mesoporous Fe3O4 with crystalline walls (inverse spinel structure) has been synthesized for the first time, representing to the best of our knowledge, the first synthesis of a reduced mesoporous iron oxide. Synthesis was achieved by reducing ordered mesoporous alpha-Fe2O3 (corundum structure) to Fe3O4 spinel then to gamma-Fe2O3 by oxidation, while preserving the ordered mesostructure and crystalline walls throughout. Such solid/solid transformations demonstrate the stability of the mesostructure to structural phase transitions from the hexagonal close packed oxide subarray of alpha-Fe2O3 (corundum structure) to the cubic close packed subarray of Fe3O4 spinel and gamma-Fe2O3. Preliminary magnetic measurements reveal that the spins in both Fe3O4 and gamma-Fe2O3 are frozen at 295 K, despite the wall thickness (7 nm) being less than the lower limit for such freezing in corresponding nanoparticles (> 8 nm).
引用
收藏
页码:12905 / 12909
页数:5
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