首页> 外文会议>European Photovoltaic Solar Energy Conference and Exhibition >ULTRAFAST ELECTRONIC AND VIBRATION DYNAMICS OF PHOTOVOLTAIC POLYMER P3HT IN NON-POLAR AND POLAR SOLVENTS
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ULTRAFAST ELECTRONIC AND VIBRATION DYNAMICS OF PHOTOVOLTAIC POLYMER P3HT IN NON-POLAR AND POLAR SOLVENTS

机译:超极性和极性溶剂光伏聚合物P3HT的超快电子和振动动力学

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In our previous work, ultrafast relaxation dynamics of photoexcitation in poly(3-hexylthiophene) (P3HT) film was studied to determine the defect concentration. The present work was performed to study ultrafast dynamics of the P3HT solutions in various solvents. The ultrafast dynamics was studied by using ultrashort sub-10fs pulse, which resolves not only the electronic dynamics but also the vibration dynamics. The electronic dynamics show fast and slow relaxations with time constants of ~200fs and ~3ps, respectively. The faster time constant (~200fs) is thought be the speed of intrachain charge transfer to form a bound polaron pair in the P3HT chain, and the time constant is longer when the dipole moment of the solvent is larger. The slower time constant (~3ps) reflects the relaxation of the polaron pair also showing similar dependence on the dipole moment of the solvent. Linear prediction singular value decomposition method was used to estimate life time of the vibration modes. The dependence on the dipole moment of the solvent was opposite in the vibration lifetime compared with that in the electronic state lifetime. It shows that the vibration mode has strong interaction with the electronic excited state when the dipole moment of the solvent is large.
机译:在我们之前的工作中,研究了聚(3-己基噻吩)(P3HT)膜中运动透析的超快放松动态,以确定缺陷浓度。对本作的工作进行了研究各种溶剂中P3HT溶液的超快动态。通过使用超短的SUB-10FS脉冲研究超快动态,这不仅可以解决电子动态,而且解决了振动动力学。电子动力学分别显示出快速和缓慢的放松,分别具有〜200fs和〜3ps的时间常数。较快的时间常数(〜200fs)被认为是颈内电荷转移的速度,以在P3HT链中形成结合的极性焦焦对,并且当溶剂的偶极力矩更大时,时间常数更长。较慢的时间常数(〜3ps)反映了极化子对的松弛,也显示出类似于溶剂的偶极力矩的类似依赖性。线性预测奇异值分解方法用于估计振动模式的寿命时间。与电子状态寿命相比,对溶剂的偶极力矩的依赖性在振动寿命中相反。它表明,当溶剂的偶极力矩大时,振动模式具有与电子激发态的强烈相互作用。

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