Coherent ultrafast charge transfer in an organic photovoltaic blend

被引:472
作者
Falke, Sarah Maria [1 ,2 ]
Rozzi, Carlo Andrea [3 ]
Brida, Daniele [4 ,5 ,6 ]
Maiuri, Margherita [4 ]
Amato, Michele [7 ]
Sommer, Ephraim [1 ,2 ]
De Sio, Antonietta [1 ,2 ]
Rubio, Angel [8 ,9 ,10 ,11 ]
Cerullo, Giulio [4 ]
Molinari, Elisa [3 ,12 ]
Lienau, Christoph [1 ,2 ]
机构
[1] Carl von Ossietzky Univ Oldenburg, Inst Phys, D-26129 Oldenburg, Germany
[2] Carl von Ossietzky Univ Oldenburg, Ctr Interface Sci, D-26129 Oldenburg, Germany
[3] CNR, Ist Nanosci, Ctr S3, Via Campi 213a, I-41125 Modena, Italy
[4] Politecn Milan, CNR, Dipartimento Fis, Ist Foton & Nanotecnol, I-20133 Milan, Italy
[5] Univ Konstanz, Dept Phys, D-78457 Constance, Germany
[6] Univ Konstanz, Ctr Appl Photon, D-78457 Constance, Germany
[7] Univ Paris Sud, CNRS, UMR8622, Inst Elect Fondamentale, F-91405 Orsay, France
[8] Univ Basque Country, Euskal Herriko Unibertsitatea, Ctr Phys Mat, CSIC,Nanobio Spect Grp, San Sebastian 20018, Spain
[9] Univ Basque Country, Euskal Herriko Unibertsitatea, European Theoret Spect Facil Sci Dev Ctr, CSIC,Nanobio Spect Grp,Dept Fis Mat,Mat Phys Ctr, San Sebastian 20018, Spain
[10] Donostia Int Phys Ctr, San Sebastian 20018, Spain
[11] Max Planck Gesell, Fritz Haber Inst, D-14195 Berlin, Germany
[12] Univ Modena & Reggio Emilia, Dipartimento Sci Fis Informat & Matemat, I-41125 Modena, Italy
基金
欧洲研究理事会;
关键词
PHOTOINDUCED ELECTRON-TRANSFER; EXCITON DISSOCIATION; CARRIER GENERATION; SOLAR-CELLS; POLYMER; SEPARATION; DYNAMICS; P3HT/PCBM; NETWORK; ENERGY;
D O I
10.1126/science.1249771
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
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.
引用
收藏
页码:1001 / 1005
页数:5
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