介孔二氧化硅
胶束
小角中子散射
中子散射
纳米颗粒
肺表面活性物质
介孔材料
化学工程
粒子(生态学)
吸附
化学物理
化学
粒径
纳米技术
材料科学
散射
有机化学
物理化学
催化作用
光学
物理
工程类
地质学
水溶液
海洋学
作者
Martin J. Hollamby,Dimitriya Borisova,Paul D. Brown,Julian Eastoe,Isabelle Grillo,Dmitry G. Shchukin
出处
期刊:Langmuir
[American Chemical Society]
日期:2011-11-01
卷期号:28 (9): 4425-4433
被引量:63
摘要
Since the first development of surfactant-templated mesoporous silicas, the underlying mechanisms behind the formation of their structures have been under debate. Here, for the first time, time-resolved small-angle neutron scattering (tr-SANS) is applied to study the complete formation of mesoporous silica nanoparticles. A distinct advantage of this technique is the ability to detect contributions from the whole system, enabling the visualization not only of particle genesis and growth but also the concurrent changes to the coexistent micelle population. In addition, using contrast-matching tr-SANS, it is possible to highlight the individual contributions from the silica and surfactant. An analysis of the data agrees well with the previously proposed "current bun" model describing particle growth: Condensing silica oligomers adsorb to micelles, reducing intermicellar repulsion and resulting in aggregation to form initial particle nuclei. From this point, the growth occurs in a cooperative manner, with condensing silica filling the gaps between further aggregating micelles. The mechanistic results are discussed with respect to different reaction conditions by changing either the concentration of the silica precursor or the temperature. In doing so the importance of in situ techniques is highlighted, in particular, tr-SANS, for mechanism elucidation in the broad field of materials science.
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