Yadavalli Nataraja Sekhar, Loebner Sarah, Papke Thomas, Sava Elena, Hurduc Nicolae, Santer Svetlana
Department of Experimental Physics, Institute of Physics and Astronomy, University of Potsdam, 14476 Potsdam, Germany.
Department of Natural and Synthetic Polymers, Gheorghe Asachi Technical University of Iasi, Prof. Dimitrie Mangeron Street, 73, 700050-Iasi, Romania.
Soft Matter. 2016 Mar 7;12(9):2593-603. doi: 10.1039/c6sm00029k.
In this paper two groups supporting different views on the mechanism of light induced polymer deformation argue about the respective underlying theoretical conceptions, in order to bring this interesting debate to the attention of the scientific community. The group of Prof. Nicolae Hurduc supports the model claiming that the cyclic isomerization of azobenzenes may cause an athermal transition of the glassy azobenzene containing polymer into a fluid state, the so-called photo-fluidization concept. This concept is quite convenient for an intuitive understanding of the deformation process as an anisotropic flow of the polymer material. The group of Prof. Svetlana Santer supports the re-orientational model where the mass-transport of the polymer material accomplished during polymer deformation is stated to be generated by the light-induced re-orientation of the azobenzene side chains and as a consequence of the polymer backbone that in turn results in local mechanical stress, which is enough to irreversibly deform an azobenzene containing material even in the glassy state. For the debate we chose three polymers differing in the glass transition temperature, 32 °C, 87 °C and 95 °C, representing extreme cases of flexible and rigid materials. Polymer film deformation occurring during irradiation with different interference patterns is recorded using a homemade set-up combining an optical part for the generation of interference patterns and an atomic force microscope for acquiring the kinetics of film deformation. We also demonstrated the unique behaviour of azobenzene containing polymeric films to switch the topography in situ and reversibly by changing the irradiation conditions. We discuss the results of reversible deformation of three polymers induced by irradiation with intensity (IIP) and polarization (PIP) interference patterns, and the light of homogeneous intensity in terms of two approaches: the re-orientational and the photo-fluidization concepts. Both agree in that the formation of opto-mechanically induced stresses is a necessary prerequisite for the process of deformation. Using this argument, the deformation process can be characterized either as a flow or mass transport.
在本文中,两组对光致聚合物变形机制持有不同观点的人员就各自潜在的理论概念展开了争论,以便让科学界关注这场有趣的辩论。尼古拉·胡尔杜克教授所在的团队支持这样一种模型,即认为偶氮苯的循环异构化可能会导致含偶氮苯的玻璃态聚合物发生非热转变,进入流体状态,即所谓的光流化概念。这个概念对于直观理解作为聚合物材料各向异性流动的变形过程相当便利。斯韦特兰娜·桑特教授所在的团队支持重定向模型,该模型指出,聚合物变形过程中聚合物材料的质量传输是由偶氮苯侧链的光致重定向以及聚合物主链的重定向所产生的,这进而会导致局部机械应力,这种应力足以使含偶氮苯的材料即使在玻璃态下也发生不可逆变形。为了这场辩论,我们选择了三种玻璃化转变温度不同的聚合物,分别为32℃、87℃和95℃,它们代表了柔性材料和刚性材料的极端情况。使用一种自制装置记录在不同干涉图案照射下聚合物薄膜的变形情况,该装置结合了用于产生干涉图案的光学部件和用于获取薄膜变形动力学的原子力显微镜。我们还展示了含偶氮苯聚合物薄膜通过改变照射条件原位且可逆地切换形貌的独特行为。我们从两种方法,即重定向概念和光流化概念,来讨论由强度(IIP)和偏振(PIP)干涉图案以及均匀强度光照射引发的三种聚合物的可逆变形结果。两者都认同光机械诱导应力的形成是变形过程的必要前提。基于这一观点,变形过程既可以被描述为流动,也可以被描述为质量传输。