De Rosa Claudio, Di Girolamo Rocco, Cicolella Alessandra, Talarico Giovanni, Scoti Miriam
Dipartimento di Scienze Chimiche, Università di Napoli Federico II, Complesso Monte S. Angelo, Via Cintia, I-80126 Naples, Italy.
Polymers (Basel). 2021 Aug 4;13(16):2589. doi: 10.3390/polym13162589.
Crystallization and phase separation in the melt in semicrystalline block copolymers (BCPs) compete in defining the final solid state structure and morphology. In crystalline-crystalline di-block copolymers the sequence of crystallization of the two blocks plays a definitive role. In this work we show that the use of epitaxial crystallization on selected crystalline substrates allows achieving of a control over the crystallization of the blocks by inducing crystal orientations of the different crystalline phases and a final control over the global morphology. A sample of polyethylene--syndiotactic polypropylene (PE--sPP) block copolymers has been synthesized with a stereoselective living organometallic catalyst and epitaxially crystallized onto crystals of two different crystalline substrates, p-terphenyl (3Ph) and benzoic acid (BA). The epitaxial crystallization on both substrates produces formation of highly ordered morphologies with crystalline lamellae of sPP and PE highly oriented along one direction. However, the epitaxial crystallization onto 3Ph should generate a single orientation of sPP crystalline lamellae highly aligned along one direction and a double orientation of PE lamellae, whereas BA crystals should induce high orientation of only PE crystalline lamellae. Thanks to the use of the two selective substrates, the final morphology reveals the sequence of crystallization events during cooling from the melt and what is the dominant event that drives the final morphology. The observed single orientation of both crystalline PE and sPP phases on both substrates, indeed, indicates that sPP crystallizes first onto 3Ph defining the overall morphology and PE crystallizes after sPP in the confined interlamellar sPP regions. Instead, PE crystallizes first onto BA defining the overall morphology and sPP crystallizes after PE in the confined interlamellar PE regions. This allows for discriminating between the different crystalline phases and defining the final morphology, which depends on which polymer block crystallizes first on the substrate. This work also shows that the use of epitaxial crystallization and the choice of suitable substrate offer a means to produce oriented nanostructures and morphologies of block copolymers depending on the composition and the substrates.
半结晶嵌段共聚物(BCP)熔体中的结晶和相分离在决定最终固态结构和形态方面相互竞争。在结晶-结晶二嵌段共聚物中,两个嵌段的结晶顺序起着决定性作用。在这项工作中,我们表明,在选定的结晶基底上使用外延结晶,能够通过诱导不同结晶相的晶体取向来控制嵌段的结晶,并最终控制整体形态。使用立体选择性活性有机金属催化剂合成了聚乙烯-间同立构聚丙烯(PE-sPP)嵌段共聚物样品,并将其外延结晶到两种不同结晶基底——对三联苯(3Ph)和苯甲酸(BA)的晶体上。在这两种基底上的外延结晶都产生了高度有序的形态,其中sPP和PE的结晶片层沿一个方向高度取向。然而,在3Ph上的外延结晶应产生沿一个方向高度排列的sPP结晶片层的单一取向和PE片层的双重取向,而BA晶体应仅诱导PE结晶片层的高度取向。由于使用了这两种选择性基底,最终形态揭示了从熔体冷却过程中的结晶事件顺序以及驱动最终形态的主要事件。实际上,在两种基底上观察到的结晶PE和sPP相的单一取向表明,sPP首先在3Ph上结晶,确定了整体形态,而PE在受限的层间sPP区域中在sPP之后结晶。相反,PE首先在BA上结晶,确定了整体形态,而sPP在受限的层间PE区域中在PE之后结晶。这使得能够区分不同的结晶相并确定最终形态,最终形态取决于哪种聚合物嵌段首先在基底上结晶。这项工作还表明,使用外延结晶和选择合适的基底提供了一种手段,可根据组成和基底制备取向的嵌段共聚物纳米结构和形态。