Charge-Transfer State Dynamics Following Hole and Electron Transfer in Organic Photovoltaic Devices

被引:120
作者
Bakulin, Artem A. [1 ,2 ]
Dimitrov, Stoichko D. [3 ]
Rao, Akshay [2 ]
Chow, Philip C. Y. [2 ]
Nielsen, Christian B. [3 ]
Schroeder, Bob C. [3 ]
McCulloch, Iain [3 ]
Bakker, Huib J. [1 ]
Durrant, James R. [3 ]
Friend, Richard H. [2 ]
机构
[1] FOM Inst AMOLF, Amsterdam, Netherlands
[2] Univ Cambridge, Cavendish Lab, Cambridge CB3 0HE, England
[3] Univ London Imperial Coll Sci Technol & Med, Ctr Plast Elect, Dept Chem, London SW7 2AZ, England
来源
JOURNAL OF PHYSICAL CHEMISTRY LETTERS | 2013年 / 4卷 / 01期
基金
英国工程与自然科学研究理事会;
关键词
HOT EXCITON DISSOCIATION; CARRIER PHOTOGENERATION; SOLAR-CELLS; RECOMBINATION; POLYMER; BLENDS; SEPARATION; DEPENDENCE; EFFICIENT; ENERGY;
D O I
10.1021/jz301883y
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
The formation of bound electron-hole pairs, also called charge-transfer (CT) states, in organic-based photovoltaic devices is one of the dominant loss mechanisms hindering performance. Whereas CT state dynamics following electron transfer from donor to acceptor have been widely studied, there is not much known about the dynamics of bound CT states produced by hole transfer from the acceptor to the donor. In this letter, we compare the dynamics of CT states formed in the different charge-transfer pathways in a range of model systems. We show that the nature and dynamics of the generated CT states are similar in the case of electron and hole transfer. However the yield of bound and free charges is observed to be strongly dependent on the HOMOD-HOMOA and LUMOD-LUMOA energy differences of the material system. We propose a qualitative model in which the effects of static disorder and sampling of states during the relaxation determine the probability of accessing CT states favorable for charge separation.
引用
收藏
页码:209 / 215
页数:7
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