肺表面活性物质
反离子
介孔材料
材料科学
化学工程
纳米技术
阳离子聚合
电解质
氧化物
化学
金属
复合数
离子
复合材料
高分子化学
有机化学
催化作用
物理化学
工程类
电极
冶金
作者
Qisheng Huo,David I. Margolese,Ulrike Ciesla,Pingyun Feng,Thurman E. Gier,Peter Sieger,Rosa Leon,Pierre M. Petroff,Ferdi Schüth,Galen D. Stucky
出处
期刊:Nature
[Springer Nature]
日期:1994-03-01
卷期号:368 (6469): 317-321
被引量:2045
摘要
THE recent synthesis of silica-based mesoporous materials1,2 by the cooperative assembly of periodic inorganic and surfactant-based structures has attracted great interest because it extends the range of molecular-sieve materials into the very-large-pore regime. If the synthetic approach can be generalized to transition-metal oxide mesostructures, the resulting nanocomposite materials might find applications in electrochromic or solid-electrolyte devices3,4, as high-surface-area redox catalysts5 and as substrates for biochemical separations. We have proposed recently6 that the matching of charge density at the surfactant/inorganic interfaces governs the assembly process; such co-organization of organic and inorganic phases is thought to be a key aspect of biomineralization7. Here we report a generalized approach to the synthesis of periodic mesophases of metal oxides and cationic or anionic surfactants under a range of pH conditions. We suggest that the assembly process is controlled by electrostatic complementarity between the inorganic ions in solution, the charged surfactant head groups and—when these charges both have the same sign—inorganic counterions. We identify a number of different general strategies for obtaining a variety of ordered composite materials.
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