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非富勒烯有机太阳能电池中的超快长程电荷分离。

Ultrafast Long-Range Charge Separation in Nonfullerene Organic Solar Cells.

机构信息

Cavendish Laboratory, Department of Physics, University of Cambridge , Cambridge CB3 0HE, United Kingdom.

Center for Organic Photonics and Electronics and School of Chemistry and Biochemistry, Georgia Institute of Technology , Atlanta, Georgia 30332-0400, United States.

出版信息

ACS Nano. 2017 Dec 26;11(12):12473-12481. doi: 10.1021/acsnano.7b06575. Epub 2017 Nov 17.

Abstract

Rapid, long-range charge separation in polymer-fullerene organic solar cells (OSCs) enables electrons and holes to move beyond their Coulomb capture radius and overcome geminate recombination. Understanding the nature of charge generation and recombination mechanisms in efficient, nonfullerene-acceptor-based OSCs are critical to further improve device performance. Here we report charge dynamics in an OSC using a perylene diimide (PDI) dimer acceptor. We use transient absorption spectroscopy to track the time evolution of electroabsorption caused by the dipolar electric field generated between electron-hole pairs as they separate after ionization at the donor-acceptor interface. We show that charges separate rapidly (<1 ps) and that free charge carriers are generated very efficiently (∼90% quantum yield). However, in the PDI-based OSC, external charge extraction is impaired by faster nongeminate decay to the ground state and to lower-lying triplet states.

摘要

聚合物-富勒烯有机太阳能电池(OSCs)中的快速、长程电荷分离使电子和空穴能够超越库仑捕获半径并克服复合。了解高效、非富勒烯受体基 OSCs 中电荷产生和复合机制的本质对于进一步提高器件性能至关重要。在这里,我们报告了使用苝二酰亚胺(PDI)二聚体受体的 OSC 中的电荷动力学。我们使用瞬态吸收光谱来跟踪在施主-受体界面处离化后,由于电子-空穴对之间产生的偶极电场引起的电吸收的时间演化。我们表明电荷分离非常迅速(<1 ps),并且自由电荷载流子的产生非常有效(∼90%的量子产率)。然而,在基于 PDI 的 OSC 中,外部电荷提取受到更快的非复合衰减到基态和较低的三重态的影响。

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