Identifying Charge-Transfer States in Polymer:Fullerene Heterojunctions by Their Emission Polarization Anisotropy

被引:7
|
作者
Arndt, Andreas P. [1 ]
Gerhard, Marina [2 ,3 ]
Koch, Martin [2 ,3 ]
Lemmer, Uli [1 ,4 ]
Howard, Ian A. [4 ]
机构
[1] Karlsruhe Inst Technol, Light Technol Inst, Kaiserstr 12, D-76131 Karlsruhe, Germany
[2] Philipps Univ Marburg, Fac Phys, Renthof 5, D-35032 Marburg, Germany
[3] Philipps Univ Marburg, Ctr Mat Sci, Renthof 5, D-35032 Marburg, Germany
[4] Karlsruhe Inst Technol, Inst Microstruct Technol, Hermann von Helmholtz Pl 1, D-76344 Eggenstein Leopoldshafen, Germany
来源
JOURNAL OF PHYSICAL CHEMISTRY C | 2017年 / 121卷 / 11期
关键词
EXCITON DISSOCIATION; ELECTRONIC-STRUCTURES; CONJUGATED POLYMER; SEPARATION; DYNAMICS; RECOMBINATION; GENERATION; EFFICIENT; ACCEPTOR; DONOR;
D O I
10.1021/acs.jpcc.6b12853
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 time-resolved photoluminescence (PL) polarization anisotropy of the organic photovoltaic model systems P3HT:PC61BM and PTB7:PC71BM, and their corresponding neat polymer films. Both blends show a strong emission from interfacial charge-transfer states (CTSs); the CTS emission can be uniquely identified by its negative polarization anisotropy, which is indicative of a significant rotation of the transition dipole moment upon charge transfer at the donor acceptor interface. We also observe a spectral region showing negative anisotropy in the PL of the neat PTB7 film; this spectral region is at slightly higher energy than the blend CTS emission. This negative anisotropy is not observed in the emission spectrum of the polymer in solution. This suggests that some emissive states in the pristine PTB7 film have transition dipole moments rotated relative to the absorbing states; we interpret these to be states with a significant interchain charge-transfer character.
引用
收藏
页码:6357 / 6364
页数:8
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