Recombination Dynamics of Charge Pairs in a Push-Pull Polyfluorene-Derivative

被引:29
|
作者
Gelinas, Simon [1 ,2 ,3 ]
Kirkpatrick, James [4 ]
Howard, Ian A. [5 ]
Johnson, Kerr [3 ]
Wilson, Mark W. B. [3 ]
Pace, Giuseppina [3 ]
Friend, Richard H. [3 ]
Silva, Carlos [1 ,2 ]
机构
[1] Univ Montreal, Dept Phys, Montreal, PQ H3C 3J7, Canada
[2] Univ Montreal, Regrp Quebecois Mat Pointe, Montreal, PQ H3C 3J7, Canada
[3] Univ Cambridge, Cavendish Lab, Cambridge CB3 0HE, England
[4] Univ Oxford, Oxford Martin Sch, Oxford OX1 2JD, England
[5] Max Planck Inst Polymer Res, D-55128 Mainz, Germany
来源
JOURNAL OF PHYSICAL CHEMISTRY B | 2013年 / 117卷 / 16期
基金
加拿大创新基金会; 加拿大自然科学与工程研究理事会; 英国工程与自然科学研究理事会;
关键词
TRANSPORT PROPERTIES; SOLAR-CELLS; SPECTROSCOPY; ULTRAFAST; FILMS; HETEROJUNCTIONS; ABSORPTION; INTERFACES; EFFICIENCY; COPOLYMER;
D O I
10.1021/jp3089963
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
We investigate the properties of long-lived species in F8BT films through time-resolved photoluminescence (PL) measurements at room temperature and 10 K. The kinetics consist of an initial exponential decay (tau = 2.26 ns) followed by a weak power-law decay (I(t) alpha t(-1)) up to at least 1 ms, both of which depend weakly on temperature. From fluence-dependent PL and ultrafast transient absorption (TA) measurements, we confirm that this emission arises from the recombination of geminate charge-pairs generated through singlet-singlet annihilation. This behavior is a consequence of the donor-acceptor nature of this polymer, which enhances singlet-singlet annihilation and facilitates the formation of long-lived geminate-pairs from energetic singlet states.
引用
收藏
页码:4649 / 4653
页数:5
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