Centre de Recherche sur la Matière Divisée, CNRS/Université d'Orléans , 1b rue de la Férollerie, 45 071 Orléans Cedex 02, France.
ACS Appl Mater Interfaces. 2014 Aug 13;6(15):12146-52. doi: 10.1021/am504086x. Epub 2014 Jul 16.
Successive structural transitions in thin films of asymmetric poly(styrene)-block-poly(lactide) (PS-PLA) block copolymer samples upon exposure to tetrahydrofuran (THF) vapors have been monitored using atomic force microscopy (AFM) and both in situ and ex situ grazing incidence small-angle X-ray scattering (GISAXS). A direct link was established between the structure in the swollen state and the morphology formed in the dried state post solvent evaporation. This was related to the high incompatibility between the constituting blocks of the copolymer that thwarted the system from reaching the homogeneous disordered state in the swollen state under the specific conditions utilized in this study. Upon rapid solvent removal, the morphologies formed in the swollen state were trapped due the fast evaporation kinetics. This work provides a better understanding of the mechanisms associated with block copolymer thin film morphology changes induced by solvent vapor annealing.
使用原子力显微镜(AFM)和原位及非原位掠入射小角 X 射线散射(GISAXS)监测了不对称聚(苯乙烯)-嵌段-聚(丙交酯)(PS-PLA)嵌段共聚物样品在暴露于四氢呋喃(THF)蒸气时的薄膜中连续结构转变。在溶胀状态下的结构和在溶剂蒸发后的干燥状态下形成的形态之间建立了直接联系。这与共聚物组成嵌段之间的高不相容性有关,这种不相容性阻止了体系在本研究中使用的特定条件下溶胀状态下达到均匀无序状态。在快速去除溶剂后,由于快速的蒸发动力学,溶胀状态下形成的形态被捕获。这项工作提供了对溶剂蒸气退火诱导嵌段共聚物薄膜形态变化相关机制的更好理解。