Pathway toward Large Two-Dimensional Hexagonally Patterned Colloidal Nanosheets in Solution

被引:74
作者
Ni, Bo [1 ]
Huang, Mingjun [1 ]
Chen, Ziran [1 ]
Chen, Yingchao [3 ]
Hsu, Chih-Hao [1 ]
Li, Yiwen [1 ]
Pochan, Darrin [3 ]
Zhang, Wen-Bin [1 ,2 ]
Cheng, Stephen Z. D. [1 ]
Dong, Xue-Hui [1 ]
机构
[1] Univ Akron, Dept Polymer Sci, Akron, OH 44325 USA
[2] Peking Univ, Coll Chem & Mol Engn, Ctr Soft Matter Sci & Engn, Key Lab Polymer Chem & Phys,Minist Educ, Beijing 100871, Peoples R China
[3] Univ Delaware, Dept Mat Sci & Engn, Newark, DE 19716 USA
基金
美国国家科学基金会;
关键词
BLOCK-COPOLYMERS; MOLECULAR NANOPARTICLES; DIBLOCK COPOLYMERS; SHAPE AMPHIPHILES; MICELLES; SURFACTANTS; ASSEMBLIES; MORPHOLOGIES; VESICLES; ORIGINS;
D O I
10.1021/ja511694a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We report the solution self-assembly of an ABC block terpolymer consisting of a polystyrene-block-poly(ethylene oxide) (PS-b-PEO) diblock copolymer tail tethered to a fluorinated polyhedral oligomeric silsesquioxane (FPOSS) cage in 1,4-dioxane/water. With increasing water content, abundant unconventional morphologies, including circular cylinders, two-dimensional hexagonally patterned colloidal nanosheets, and laterally patterned vesicles, are sequentially observed. The formation of toroids is dominated by two competing free energies: the end-cap energy of cylinders and the bending energy to form the circular structures. Incorporating the superhydrophobic FPOSS cages enhances the end-cap energy and promotes toroid formation. Lateral aggregation and fusion of the cylinders results in primitive nanosheets that are stabilized by the thicker rims to partially release the rim-cap energy. Rearrangement of the parallel-aligned FPOSS cylindrical cores generates hexagonally patterned nanosheets. Further increasing the water content induces the formation of vesicles with nanopatterned walls.
引用
收藏
页码:1392 / 1395
页数:4
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