Ultrafast Terahertz Photoconductivity of Photovoltaic Polymer-Fullerene Blends: A Comparative Study Correlated with Photovoltaic Device Performance

被引:54
作者
Jin, Zuanming [1 ]
Gehrig, Dominik [1 ]
Dyer-Smith, Clare [1 ]
Heilweil, Edwin J. [2 ]
Laquai, Frederic [1 ]
Bonn, Mischa [1 ]
Turchinovich, Dmitry [1 ]
机构
[1] Max Planck Inst Polymer Res, D-55128 Mainz, Germany
[2] NIST, Gaithersburg, MD 20899 USA
来源
JOURNAL OF PHYSICAL CHEMISTRY LETTERS | 2014年 / 5卷 / 21期
关键词
SOLAR-CELLS; CARRIER DYNAMICS; QUANTUM EFFICIENCY; SPECTROSCOPY; MOBILITIES; GENERATION; COPOLYMER;
D O I
10.1021/jz501890n
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
Ultrafast photoinduced carrier dynamics in prototypical low band gap polymer:fullerene photovoltaic blend films PTB7:PC70BM and P3HT:Pe(70)BM is investigated using ultrafast terahertz (THz) spectroscopy. The subpicosecond and fewpicosecond decays of THz-probed photoconductivities for both compounds are observed, attributed to the rapid formation of polaron pairs by exciton-exciton annihilation and subsequent polaron pair annihilation, respectively. The transient THz photoconductivity spectra of PTB7:PC70BM are well described by the Drude-Smith (DS) model, directly yielding the important charge transport parameters such as charge carrier density, momentum scattering time, and effective localization. By comparison with P3HT:PC70BM, we find that in PTB7:PC70BM the mobile charge carrier photoconductivity is significantly enhanced by a factor of 1.8 and prevails for longer times after charge formation, due to both improved mobile charge carrier yield and lower charge localization. In PTB7:PC70BM, a strong dependency of electron momentum scattering time on electron density was found, well parametrized by the empirical Caughey-Thomas model. The difference in ultrafast photoconductivities of both P3HT:PC70BM and PTB7:PC70BM is found to correlate very well with the performance of photovoltaic devices based on those materials.
引用
收藏
页码:3662 / 3668
页数:7
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