杀菌剂
介孔二氧化硅
纳米颗粒
介孔材料
材料科学
介孔有机硅
芯(光纤)
壳体(结构)
纳米技术
化学工程
化学
催化作用
有机化学
复合材料
工程类
生物
植物
作者
Leilei Luo,Yucang Liang,Egil S. Erichsen,Reiner Anwander
标识
DOI:10.1002/chem.201800135
摘要
Abstract A new class of hierarchically structured mesoporous silica core–shell nanoparticles (HSMSCSNs) with a periodic mesoporous organosilica (PMO) core and a mesoporous silica (MS) shell is reported. The applied one‐pot, two‐step strategy allows rational control over the core/shell chemical composition, topology, and pore/particle size, simply by adjusting the reaction conditions in the presence of cetyltrimethylammonium bromide (CTAB) as structure‐directing agent under basic conditions. The spherical, ethylene‐ or methylene‐bridged PMO cores feature hexagonal ( p 6 mm ) or cage‐like cubic symmetry ( Pm n ) depending on the organosilica precursor. The hexagonal MS shell was obtained by n ‐hexane‐induced controlled hydrolysis of TEOS followed by directional co‐assembly/condensation of silicate/CTAB composites at the PMO cores. The HSMSCSNs feature a hierarchical pore structure with pore diameters of about 2.7 and 5.6 nm in the core and shell domains, respectively. The core sizes and shell thicknesses are adjustable in the ranges of 90–275 and 15–50 nm, respectively, and the surface areas (max. 1300 m 2 g −1 ) and pore volumes (max. 1.83 cm 3 g −1 ) are among the highest reported for core–shell nanoparticles. The adsorption and controlled release of the fungicide propiconazole by the HSMSCSNs showed a three‐stage release profile.
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