Photoinduced Dynamics of Charge Separation: From Photosynthesis to Polymer-Fullerene Bulk Heterojunctions

被引:49
作者
Niklas, Jens [1 ]
Beaupre, Serge [2 ]
Leclerc, Mario [2 ]
Xu, Tao [3 ,4 ]
Yu, Luping [3 ,4 ]
Sperlich, Andreas [5 ,6 ]
Dyakonov, Vladimir [5 ,6 ]
Poluektov, Oleg G. [1 ]
机构
[1] Argonne Natl Lab, Chem Sci & Engn Div, 9700 S Cass Ave, Argonne, IL 60439 USA
[2] Univ Laval, Dept Chem, Quebec City, PQ G1V 0A6, Canada
[3] Univ Chicago, Dept Chem, Chicago, IL 60637 USA
[4] Univ Chicago, James Franck Inst, Chicago, IL 60637 USA
[5] Univ Wurzburg, D-97074 Wurzburg, Germany
[6] Bavarian Ctr Appl Energy Res ZAE Bayern, D-97074 Wurzburg, Germany
基金
加拿大自然科学与工程研究理事会;
关键词
ELECTRON-SPIN POLARIZATION; CORRELATED RADICAL PAIRS; REACTION CENTERS; PARAMAGNETIC-RESONANCE; PULSED EPR; MULTIFREQUENCY EPR; PHOTOSYSTEM-I; TRIPLET-STATE; SPECTROSCOPY; DISTANCE;
D O I
10.1021/jp511021v
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Understanding charge separation and charge transport is crucial for improving the efficiency of organic solar cells. Their active media are based on organic molecules and polymers, serving as both light-absorbing and transport layers. The charge-transfer (CT) states play an important role, being intermediate for free carrier generation and charge recombination. Here, we use light-induced electron paramagnetic resonance spectroscopy to study the CT dynamics in blends of the polymers P3HT, PCDTBT, and PTB7 with the fullerene derivative C-60-PCBM. Time-resolved EPR measurements show strong spin-polarization patterns for all polymer-fullerene blends, confirming predominant generation of singlet CT states and partial orientation ordering near the donor-acceptor interface. These observations allow a comparison with charge separation processes in molecular donor-acceptor systems and in natural and artificial photosynthetic assemblies, and thus the elucidation of the initial steps of sequential CT in organic photovoltaic materials.
引用
收藏
页码:7407 / 7416
页数:10
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