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New Insight on Photoisomerization Kinetics of Photo-Switchable Thin Films Based on Azobenzene/Graphene Hybrid Additives in Polyethylene Oxide

机译:基于聚环氧乙烷/石墨烯杂交添加剂的光学切换薄膜光致硅化动力学的新见解

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摘要

In this work, we reported a new insight on the kinetics of photoisomerization and time evolution of hybrid thin films considering the azo-dye methyl red (MR) incorporated with graphene accommodated in polyethylene oxide (PEO). The kinetics of photoisomerization and time-evolution of hybrid thin films were investigated using UV-Vis s and FTIR spectroscopies, as well as appropriate models developed with new analytical methods. The existence of azo-dye MR in the complex is crucial for the resource action of the trans↔cis cycles through UV-illumination ↔ Visible-illumination relaxations. The results of the UV–Vis and the FTIR investigations prove the cyclical trans ↔ cis-states. Consequently, PEO-(MR-Graphene) hybrid composite thin films can be introduced as possible applicants for photochromic molecular switches, light-gated transistors, and molecular solar thermal energy storage media.
机译:在这项工作中,考虑到包含在聚环氧烯(PEO)中的石墨烯的偶氮染料甲基红色(MR),对杂交薄膜的光学薄膜的动力学和时间演化的新见解。使用UV-Vis S和FTIR光谱研究了杂交薄膜的光致硅化和时间演化的动力学,以及用新的分析方法开发的适当模型。复杂中的偶氮染料的存在对于跨域的资源行为至关重要↔通过紫外线照明的顺式循环↔可见光放松。 UV-Vis和FTIR调查的结果证明了周期性的反式↔CIS-国家。因此,可以将PEO-(MR-石墨烯)混合复合薄膜作为光致变色分子开关,光门控晶体管和分子太阳能热能存储介质引入可能的申请人。

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