富勒烯
飞秒
离域电子
化学物理
电荷(物理)
振动耦合
材料科学
超短脉冲
电子转移
激发
有机太阳能电池
电子受体
女性化学
接受者
电子
光化学
聚合物
化学
原子物理学
激发态
物理
激光器
光学
有机化学
凝聚态物理
量子力学
复合材料
作者
Sarah M. Falke,Carlo Andrea Rozzi,Daniele Brida,Margherita Maiuri,Michele Amato,Ephraim Sommer,Antonietta De Sio,Ángel Rubio,Giulio Cerullo,Elisa Molinari,Christoph Lienau
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2014-05-29
卷期号:344 (6187): 1001-1005
被引量:505
标识
DOI:10.1126/science.1249771
摘要
Blends of conjugated polymers and fullerene derivatives are prototype systems for organic photovoltaic devices. The primary charge-generation mechanism involves a light-induced ultrafast electron transfer from the light-absorbing and electron-donating polymer to the fullerene electron acceptor. Here, we elucidate the initial quantum dynamics of this process. Experimentally, we observed coherent vibrational motion of the fullerene moiety after impulsive optical excitation of the polymer donor. Comparison with first-principle theoretical simulations evidences coherent electron transfer between donor and acceptor and oscillations of the transferred charge with a 25-femtosecond period matching that of the observed vibrational modes. Our results show that coherent vibronic coupling between electronic and nuclear degrees of freedom is of key importance in triggering charge delocalization and transfer in a noncovalently bound reference system.
科研通智能强力驱动
Strongly Powered by AbleSci AI