A facile route to synthesize a new type of multifunctional nanocomposites is reported. Here, PDMAEMA （poly[2- （dimethylamino）ethyl] methacrylate） is a key macromolecule serving as a bridge between magnetic FeaO3 nanoparticles and luminescent quantum dots. Both Fe203 nanoparticles and II-VI semiconductor quantum dots with a narrow size distribution are synthesized through a two-phase thermal approach. Subsequently, the atom transfer radical polymerization （ATRP） technique was applied to prepare magnetic Fe203@PDMAEMA core-shell nanoparticles. The thickness of PDMAEMA shell can be easily controlled by adjusting the reaction time. Finally, the ligand exchange method was exploited to modify II-VI quantum dot with amine-containing polymer of PDMAEMA, which led to quantum dot securely bound by Fe203@PDMAEMA core-shell nanoparticle to form a multifunctional nanocomposite. The resulting nanocomposite remains variable emission by tuning the II-VI semiconductor type and particle size and shows/arc at 49 kA/m and Tb at 16 K from Fe2O3 nanoparticles. The self-assembled behavior for the resulting samples is also discussed.
In this work, monodisperse giant polymersomes are fabricated by dewetting of water-in-oil-in-water double emulsion droplets which are assembled by amphiphilic block copolymer molecules in a microfluidic device. The dewetting process can be tuned by solvation between solvent and amphiphilic block copolymer to get polymersomes with controllable morphology. Good solvent （chloroform and toluene） hinders dewetting process of double emulsion droplets and gets acornlike polymersomes or patched polymersomes. On the other hand, poor solvent （hexane） accelerates the dewetting process and achieves complete separation of inner water phase from oil phase to form complete bilayer polymersomes. In addition, twin polymersomes with bilayer membrane structure are formed by this facile method. The formation mechanism for different polymersomes is discussed in detail.
