Vesicular mesoporous silica with well-defined multilamellar structures was prepared using didodecyldimethylammonium bromide (DDAB)/cetyltrimethylammonium bromide (CTAB) as a structure-directing agent. The number of vesicular silica layers can be tuned from 7 to 2 by changing the molar ratio of DDAB to CTAB.

An improved strategy to synthesize SiO2‐PMMA nanoparticles with tunable shell thickness is demonstrated, via iron (III) catalyst‐mediated activators generated by electron transfer for atom transfer radical polymerization (AGET ATRP). To investigate the effect of the content monomer and ligand on the PMMA shell thickness, hydrophobic PMMA‐PSt diblock copolymer brushes on the surface of the silica nanospheres are designed and synthesized by AGET ATRP. Transmission electron microscopy (TEM) and field‐emission scanning electron microscopy (FESEM) show that the product has a core‐shell‐like structure and that the average shell thickness of the PMMA can easily be tuned by simply adjusting the amount of monomer or ligand. In addition, the Mn of the PMMA can be tuned from 37 800 to 62 400 g mol−1 by changing the shell thickness, and the PDI is 1.213–1.473. These results confirm the living nature of the polymerization.

SiO₂-based composites have important applications in various technological fields. In this work, a tunablevoid SiO₂-TiO₂ core-shell structure was successfully prepared for the first time using SiO₂-polymethyl methacrylate (PMMA)-polyoligo(ethylene glycol)methyl ether methacrylate (PO(EO)nMA) (n = 2, 5, and 8). An amphiphilic copolymer was used as the template, and calcination was performed using tetrabutyl titanate (TBT) as the titanium source. SiO₂-PMMA-b-PO(EO)nMA microspheres were first synthesized through activators regenerated by electron transfer-atom transfer radical polymerization. Methyl methacrylate and O(EO)nMA were grafted with different EO unit numbers onto the surface of the halogen functional group of SiO₂. TBT was hydrolyzed along with the PO(EO)nMA chain through hydrogen bonding, and then the SiO₂-TiO₂ core-shell structure was acquired through calcination to remove the polymer. Simultaneously, amorphous TiO₂ crystallized during calcination. A series of characterizations indicated that the amphiphilic block copolymer was grafted onto SiO₂ mesoparticle surfaces, the titania samples existed only in the anatase phase, and the prepared SiO₂-TiO₂ had hierarchically nanoporous structures. The gradient hydrophilicity of the PMMA-b-PO(EO)nMA copolymer template facilitated the hydrolysis of TBT molecules along the PO(EO)nMA to PMMA segments, thereby tuning the space between the core and the shell. In addition, the space was about 6 nm when the EO number was 2, and the space was about 10 nm when the EO numbers were 5 and 8. The photocatalytic activities of the SiO₂-TiO₂ materials were tested on the photodegradation of methyl orange.

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