Extended Charge Carrier Lifetimes in Hierarchical Donor Acceptor Supramolecular Polymer Films

被引:25
|
作者
Guzman, Carmen X. [1 ]
Calderon, Rafael M. Krick [1 ]
Li, Zhong [1 ]
Yamazaki, Shiori [1 ]
Peurifoy, Samuel R. [1 ]
Guo, Chengchen [2 ]
Davidowski, Stephen K. [2 ]
Mazza, Mercedes M. A. [1 ]
Han, Xu [1 ]
Holland, Gregory [3 ]
Scott, Amy M. [1 ]
Braunschweig, Adam B. [1 ]
机构
[1] Univ Miami, Dept Chem, Coral Gables, FL 33146 USA
[2] Arizona State Univ, Dept Chem & Biochem, Magnet Resonance Res Ctr, Tempe, AZ 85287 USA
[3] San Diego State Univ, Dept Chem & Biochem, San Diego, CA 92182 USA
来源
JOURNAL OF PHYSICAL CHEMISTRY C | 2015年 / 119卷 / 34期
基金
美国国家科学基金会;
关键词
PHOTOINDUCED ELECTRON-TRANSFER; MOLECULE SOLAR-CELLS; ARTIFICIAL PHOTOSYNTHESIS; PI STACKING; SEPARATION; RECOMBINATION; ENERGY; PERYLENEDIIMIDE; SUPERSTRUCTURES; SEMICONDUCTORS;
D O I
10.1021/acs.jpcc.5b03713
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 report that supramolecular polymer films composed of a 2:1 mixture of monodiamidopyridine diketopyrrolopyrrole (DPP) electron donors and perylene bisdiimide (PDI) electron acceptors undergo photoinduced charge transfer in the solid state. Film formation is guided by complementary noncovalent interactions programmed into the molecular components, resulting in a film architecture comprised of polymer wires with order across the molecular-to-macroscopic continuum. Using ultrafast transient absorption spectroscopy, we show that recombination lifetimes increase 1000-fold compared to the same supramolecular polymers in solution. Supramolecular donor-acceptor polymer films, such as these, that are designed by considering structure and electron transfer dynamics synergistically could lead to breakthroughs in organic optoelectronics.
引用
收藏
页码:19584 / 19589
页数:6
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