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Degradation‐Restructuring Induced Anisotropic Epitaxial Growth for Fabrication of Asymmetric Diblock and Triblock Mesoporous Nanocomposites
Author(s) -
Li Xiaomin,
Zhao Tiancong,
Lu Yang,
Wang Peiyuan,
ElToni Ahmed Mohamed,
Zhang Fan,
Zhao Dongyuan
Publication year - 2017
Publication title -
advanced materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 10.707
H-Index - 527
eISSN - 1521-4095
pISSN - 0935-9648
DOI - 10.1002/adma.201701652
Subject(s) - materials science , nanorod , mesoporous material , mesoporous silica , nanocomposite , mesoporous organosilica , nanotechnology , fabrication , chemical engineering , organic chemistry , catalysis , medicine , chemistry , alternative medicine , pathology , engineering
A novel degradation‐restructuring induced anisotropic epitaxial growth strategy is demonstrated for the synthesis of uniform 1D diblock and triblock silica mesoporous asymmetric nanorods with controllable rod length (50 nm to 2 µm) and very high surface area of 1200 m 2 g −1 . The asymmetric diblock mesoporous silica nanocomposites are composed of a 1D mesoporous organosilicate nanorod with highly ordered hexagonal mesostructure, and a closely connected dense SiO 2 nanosphere located only on one side of the nanorods. Furthermore, the triblock mesoporous silica nanocomposites constituted by a cubic mesostructured nanocube, a nanosphere with radial mesopores, and a hexagonal mesostructured nanorod can also be fabricated with the anisotropic growth of mesopores. Owing to the ultrahigh surface area, unique 1D mesochannels, and functionality asymmetry, the obtained match‐like asymmetric Au‐NR@SiO 2 &EPMO (EPMO = ethane bridged periodic mesoporous organosilica) mesoporous nanorods can be used as an ideal nanocarrier for the near‐infrared photothermal triggered controllable releasing of drug molecules.