Degradation-Restructuring Induced Anisotropic Epitaxial Growth for Fabrication of Asymmetric Diblock and Triblock Mesoporous Nanocomposites

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 m² 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 SiO₂ 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@SiO₂&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.

A novel degradation-restructuring induced anisotropic epitaxial growth strategy is demonstrated for the synthesis of uniform 1D asymmetric diblock and triblock mesoporous nanorods.

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