† Key Laboratory of Large-Format Battery Materials and Systems of the Ministry of Education, School of Chemistry and Chemical Engineering, Huazhong University of Science and Technology, Wuhan 430074, P. R. China
‡ State Key Laboratory of Polymer Physics and Chemistry, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, P. R. China
Macromolecules, 2013, 46 (17), pp 7012–7017
DOI: 10.1021/ma401398h
Section:Abstract
A reversible transformation of overall shape and internal structure as well as surface composition of nanostructured block copolymer particles is demonstrated by solvent-adsorption annealing. Polystyrene--poly(4-vinylpyridine) (PS--P4VP) pupa-like particles with PS and P4VP lamellar domains alternatively stacked can be obtained by self-assembly of the block copolymer under 3D soft confinement. Chloroform, a good solvent for both blocks, is selected to swell and anneal the pupa-like particles suspended in aqueous media. Reversible transformation between pupa-like and onion-like structures of the particles can be readily tuned by simply adjusting the particle/aqueous solution interfacial property. Interestingly, poly(vinyl alcohol) (PVA) concentration in the aqueous media plays a critical role in determining the particle morphology. High level of PVA concentration is favorable for pupa-like morphology, while extremely low concentration of PVA is favorable for the formation of onion-like particles. Moreover, the stimuli-response behavior of the particles can be highly suppressed through selective growth of Au nanoparticles within the P4VP domains. This strategy provides a new concept for the reversible transformation of nanostructured polymer particles, which will find potential applications in the field of sensing, detection, optical devices, drug delivery, and smart materials fabrication.
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