期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 126, 期 25, 页码 7940-7945出版社
AMER CHEMICAL SOC
DOI: 10.1021/ja049453k
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资金
- NCI NIH HHS [N01-CO-17016-32] Funding Source: Medline
- NIGMS NIH HHS [GM58821] Funding Source: Medline
We developed a process to fabricate 150-700 nm monodisperse polymer particles with 100500 nm hollow cores. These hollow particles were fabricated via dispersion polymerization to synthesize a polymer shell around monodisperse SiO2 particles. The SiO2 cores were then removed by HF etching to produce monodisperse hollow polymeric particle shells. The hollow core size and the polymer shell thickness, can be easily varied over significant size ranges. These hollow polymeric particles are sufficiently monodisperse that upon centrifugation from ethanol they form well-ordered close-packed colloidal crystals that diffract light. After the surfaces are functionalized with sulfonates, these particles self-assemble into crystalline colloidal arrays in deionized water. This synthetic method can also be used to create monodisperse particles with complex and unusual morphologies. For example, we synthesized hollow particles containing two concentric-independent, spherical polymer shells, and hollow silica particles which contain a central spherical silica core. In addition, these hollow spheres can be used as template microreactors. For example, we were able to fabricate monodisperse polymer spheres containing high concentrations of magnetic nanospheres formed by direct precipitation within the hollow cores.
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