Panagopoulou Anna, Rodríguez-Tinoco Cristian, White Ronald P, Lipson Jane E G, Napolitano Simone
Laboratory of Polymer and Soft Matter Dynamics, Experimental Soft Matter and Thermal Physics (EST), Faculté des Sciences, Université libre de Bruxelles (ULB), Boulevard du Triomphe, Bruxelles 1050, Belgium.
Department of Chemistry, Dartmouth College, Hanover, New Hampshire 03755, USA.
Phys Rev Lett. 2020 Jan 17;124(2):027802. doi: 10.1103/PhysRevLett.124.027802.
We show that the segmental mobility of thin films of poly(4-chlorostyrene) prepared under nonequilibrium conditions gets enhanced in the proximity of rough substrates. This trend is in contrast to existing treatments of roughness which conclude it is a source of slower dynamics, and to measurements of thin films of poly(2-vinylpiridine), whose dynamics is roughness invariant. Our experimental evidence indicates the faster interfacial dynamics originate from a reduction in interfacial density, due to the noncomplete filling of substrate asperities. Importantly, our results agree with the same scaling that describes the density dependence of bulk materials, correlating segmental mobility to a term exponential in the specific volume, and with empirical relations linking an increase in glass transition temperature to larger interfacial energy.
我们表明,在非平衡条件下制备的聚(4-氯苯乙烯)薄膜的链段迁移率在粗糙基底附近会增强。这一趋势与现有关于粗糙度的理论相反,现有理论认为粗糙度是动力学变慢的一个原因,同时也与聚(2-乙烯基吡啶)薄膜的测量结果相反,后者的动力学与粗糙度无关。我们的实验证据表明,较快的界面动力学源于界面密度的降低,这是由于基底粗糙处未被完全填满所致。重要的是,我们的结果与描述块状材料密度依赖性的相同标度关系一致,即将链段迁移率与比容的指数项相关联,并且与将玻璃化转变温度升高与更大界面能联系起来的经验关系一致。