Department of Chemical and Biomolecular Engineering, Korea Advanced Institute of Science and Technology (KAIST), Daejeon 305-701, Republic of Korea.
ACS Nano. 2012 Mar 27;6(3):2750-7. doi: 10.1021/nn300194z. Epub 2012 Mar 6.
Gold-decorated block copolymer microspheres (BCP-microspheres) displaying various surface morphologies were prepared by the infiltration of Au precursors into polystyrene-b-poly(4-vinylpyridine) (PS-b-P4VP) microspheres. The microspheres were fabricated by emulsifying the PS-b-P4VP polymers in chloroform into a surfactant solution in water, followed by the evaporation of chloroform. The selective swelling of the P4VP domains in the microspheres by the Au precursor under acidic conditions resulted in the formation of Au-decorated BCP-microspheres with various surface nanostructures. As evidenced by transmission electron microscopy (TEM) and scanning electron microscopy (SEM) measurements, dotted surface patterns were formed when microspheres smaller than 800 nm were synthesized, whereas fingerprint-like surface patterns were observed with microspheres larger than 800 nm. Au nanoparticles (NPs) were located inside P4VP domains near the surfaces of the prepared microspheres, as confirmed by TEM. The optical properties of the BCP-microspheres were characterized using UV-vis absorption spectroscopy and fluorescence lifetime measurements. A maximum absorption peak was observed at approximately 580 nm, indicating that Au NPs are densely packed into P4VP domains on the microspheres. Our approach for creating Au-NP-hybrid BCP-microspheres can be extended to other NP systems such as iron-oxide or platinum NPs. These precursors can also be selectively incorporated into P4VP domains and induce the formation of hybrid BCP-microspheres with controlled surface nanostructures.
金修饰的嵌段共聚物微球(BCP-微球)展示了各种表面形态,是通过将金前体渗透到聚苯乙烯-聚(4-乙烯基吡啶)(PS-b-P4VP)微球中制备的。微球是通过将 PS-b-P4VP 聚合物在氯仿中乳化到水中的表面活性剂溶液中,然后蒸发氯仿来制备的。在酸性条件下,P4VP 畴对金前体的选择性溶胀导致形成具有各种表面纳米结构的 Au 修饰的 BCP-微球。正如透射电子显微镜(TEM)和扫描电子显微镜(SEM)测量所证明的那样,当合成小于 800nm 的微球时,形成点状表面图案,而大于 800nm 的微球则观察到指纹状表面图案。TEM 证实,Au 纳米颗粒(NPs)位于制备的微球表面附近的 P4VP 畴内。使用紫外-可见吸收光谱和荧光寿命测量来表征 BCP-微球的光学性质。在大约 580nm 处观察到最大吸收峰,表明 Au NPs 被密集地填充到微球上的 P4VP 畴中。我们用于创建 Au-NP-杂化 BCP-微球的方法可以扩展到其他 NP 系统,例如氧化铁或铂 NPs。这些前体也可以选择性地掺入 P4VP 畴中,并诱导具有受控表面纳米结构的杂化 BCP-微球的形成。