首页> 外文期刊>The journal of physical chemistry, C. Nanomaterials and interfaces >Optical absorption of poly(thienylene vinylene)-conjugated polymers: Experiment and first principle theory
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Optical absorption of poly(thienylene vinylene)-conjugated polymers: Experiment and first principle theory

机译:聚(噻吩亚乙烯撑)共轭聚合物的光吸收:实验和第一原理理论

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摘要

Optical absorption spectra of poly(thienylene vinylene) (PTV)-conjugated polymers have been studied at room temperature in the spectral range of 450-800 nm. A dominant peak located at 577 nm and a prominent shoulder at 619 nm are observed. Another shoulder located at 685 nm is observed at high concentration and after additional treatment (heat, sonification) only. Equilibrium atomic geometries and optical absorption of PTV conjugated polymers have also been studied by first principles density functional theory. For PTV in solvent, the theoretical calculations predict two equilibrium geometries with different interchain distances. By comparative analysis of the experimental and theoretical data, it is demonstrated that the new measured long-wavelength optical absorption shoulder is consistent with new optical absorption peak predicted for most energetically favorable PTV phase in the solvent. This shoulder is interpreted as a direct indication of increased interchain interaction in the solvent which has caused additional electronic energy structure transformations.
机译:已经在室温下在450-800nm的光谱范围内研究了聚(噻吩亚乙烯基)(PTV)-共轭聚合物的光吸收光谱。观察到位于577 nm处的主要峰和位于619 nm处的突出峰。在高浓度下并且仅在进行其他处理(加热,超声处理)后,才能观察到位于685 nm处的另一个肩。还通过第一原理密度泛函理论研究了PTV共轭聚合物的平衡原子几何形状和光吸收。对于溶剂中的PTV,理论计算预测了链间距离不同的两个平衡几何。通过对实验数据和理论数据的比较分析,表明新测得的长波长光吸收肩峰与溶剂中能量最有利的PTV相预测的新光吸收峰一致。该肩峰被解释为溶剂中链间相互作用增加的直接指示,这导致了额外的电子能量结构转变。

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