Extending Long-lived Charge Separation Between Donor and Acceptor Blocks in Novel Copolymer Architectures Featuring a Sensitizer Core

被引:17
作者
Schroot, Robert [1 ,2 ]
Schlotthauer, Tina [1 ,2 ]
Dietzek, Benjamin [2 ,3 ,4 ,5 ]
Jaeger, Michael [1 ,2 ]
Schubert, Ulrich S. [1 ,2 ]
机构
[1] Friedrich Schiller Univ Jena, Lab Organ & Macromol Chem IOMC, Humboldtstr 10, D-07743 Jena, Germany
[2] Friedrich Schiller Univ Jena, Ctr Energy & Environm Chem Jena, Philosophenweg 7a, D-07743 Jena, Germany
[3] Friedrich Schiller Univ Jena, Inst Phys Chem, Helmholtzweg 4, D-07743 Jena, Germany
[4] Friedrich Schiller Univ Jena, Abbe Ctr Photon, Helmholtzweg 4, D-07743 Jena, Germany
[5] Leibniz Inst Photon Technol IPHT, Albert Einstein Str 9, D-07743 Jena, Germany
关键词
complex chemistry; donor-acceptor systems; electron transfer; ruthenium; time-resolved spectroscopy; SOLAR-ENERGY CONVERSION; ELECTRON-TRANSFER; ARTIFICIAL PHOTOSYNTHESIS; END FUNCTIONALIZATION; POLYMER; LIGHT; SEMICONDUCTORS; TRIARYLAMINES; TRANSISTORS; COMPLEX;
D O I
10.1002/chem.201704180
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A bifunctional Ru-II photosensitizer unit was decorated with one n- and one p-type polymer chain to form precisely controlled hierarchical copolymer-type architectures for light-induced charge separation. The applied modular chemistry-on-the-complex strategy benefits from separately prepared building blocks and their orthogonal linkage in the two final assembly steps. Upon visible light absorption, electron transfer is initiated between the conjugated poly(3,6-carbazole) chain and the styrenic poly(naphthalene diimide) segments. Steady-state and time-resolved spectroscopy show complete charge separation within a few nanoseconds (> 95% efficiency) persisting several tens of microseconds. The recombination is significantly reduced in comparison to low-molecular model systems or to non-conjugated congeners, reflecting the higher charge mobility in conjugated polymers. In summary, the modularity of the presented approach is expected to serve as a versatile platform to tailor the interface between the charge transport domains in a systematic fashion.
引用
收藏
页码:16484 / 16490
页数:7
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