Monodisperse mesoporous silica nanoparticles of distinct topology

被引:30
作者
Luo, Leilei [1 ]
Liang, Yucang [1 ]
Erichsen, Egil Sev. [2 ]
Anwander, Reiner [1 ]
机构
[1] Univ Tubingen, Inst Anorgan Chem, Morgenstelle 18, D-72076 Tubingen, Germany
[2] Univ Bergen, Electron Microscopy Lab, Allegaten 41, N-5007 Bergen, Norway
关键词
Mesoporous silica; Nanoparticles; Morphology; Topology; Monodispersity; MCM-48; PARTICLE-SIZE CONTROL; IN-SITU; MOLECULAR-SIEVES; X-RAY; FACILE SYNTHESIS; FORMATION MECHANISM; CONTROLLED-RELEASE; MCM-48; PHASE; ALCOHOL;
D O I
10.1016/j.jcis.2017.01.107
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Monodisperse and uniform high-quality MCM(Mobil Composition of Matter)-48-type CMSNs (Cubic Mesoporous Silica Nanoparticles) are readily prepared by simply optimizing the molar ratio of ethanol and surfactant in the system TEOS-CTAB-NaOH-H2O-EtOH (TEOS = tetraethyl orthosilicate, CTAB = cetyltrimethylammonium bromide, EtOH = ethanol). In the absence of ethanol only hexagonal mesoporous silica with ellipsoidal and spherical morphology are obtained. The presence of ethanol drives a mesophase transformation from hexagonal to mixed hexagonal/cubic, further to purely cubic, and finally to a mixed cubic/lamellar. This is accompanied by a morphology evolution involving a mixture of ellipses/spheres, regular rods, uniform spheres, and finally a mixture of spheres/flakes. Preserving the three-dimensional (3D) cubic MCM-48 structure, use of a small amount of ethanol is beneficial to the improvement of the monodispersity of the CMSNs. Moreover, the quality of the CMSNs can also be controlled by changing the surfactant concentration or adjusting the stirring rate. All MSNs were characterized using powder X-ray diffraction, transmission electron microscopy, scanning electron microscopy, and N-2 physisorption, indicating highly long-range ordered pore arrays, high specific surface areas (max. 1173 m(2) g(-1)) as well as high pore volumes (max. 1.14 cm(3) g(-1)). The monodispersity of the CMSNs was verified by statistical particle size distribution from SEM (scanning electron microscopy)/TEM (transmission electron microscopy) images and DLS (dynamic light scattering). The mesophase transformation can be rationalized on the basis of an ethanol-driven change of the surfactant packing structure and charge matching at the surfactant/silicate interface. The corresponding morphology evolution can be elucidated by an ethanol-controlled hydrolysis rate of TEOS and degree of condensation of oligomeric silicate species via a nucleation and growth process. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:84 / 93
页数:10
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