Tu Zeyi, Han Guangchao, Yi Yuanping
Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Organic Solids, CAS Research/Education Center for Excellence in Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China.
University of Chinese Academy Sciences, Beijing 100049, China.
J Phys Chem Lett. 2020 Apr 2;11(7):2585-2591. doi: 10.1021/acs.jpclett.0c00405. Epub 2020 Mar 18.
The separation of charge-transfer states into free charges at the donor/acceptor (D/A) interfaces plays a central role in organic solar cells (OSCs). Because of strong Coulomb attraction, the separation mechanisms are elusive, particularly for the high-efficiency non-fullerene (NF) OSCs with low exciton-dissociation driving forces. Here, we demonstrate that the Coulomb barriers can be substantially overcome by electronic polarization for OSCs based on a series of A-D-A acceptors (ITIC, IT-4F, and Y6). In contrast to fullerene-based D/A heterojunctions, the polarization energies for both donor holes and acceptor electrons are remarkably increased from the interfaces to pure regions in the NF heterojunctions because of strong stabilization on electrons but destabilization on holes by electrostatic interactions in the A-D-A acceptors. In particular, upon incorporation of fluorine substituents and electron-poor cores into ITIC, the increased polarization energies can completely compensate for the Coulomb attraction in the IT-4F- and Y6-based heterojunctions, leading to barrierless charge separation.
电荷转移态在供体/受体(D/A)界面处分离为自由电荷,这在有机太阳能电池(OSC)中起着核心作用。由于强烈的库仑吸引力,分离机制难以捉摸,特别是对于具有低激子解离驱动力的高效非富勒烯(NF)OSC。在这里,我们证明了基于一系列A-D-A受体(ITIC、IT-4F和Y6)的OSC,通过电子极化可以显著克服库仑势垒。与基于富勒烯的D/A异质结相比,由于A-D-A受体中的静电相互作用对电子有强烈的稳定作用,但对空穴有去稳定作用,NF异质结中供体空穴和受体电子的极化能从界面到纯区域都显著增加。特别是,在ITIC中引入氟取代基和缺电子核后,增加的极化能可以完全补偿基于IT-4F和Y6的异质结中的库仑吸引力,从而实现无势垒电荷分离。