Efficient Ternary Polymer Solar Cells with Tunable Crystallinity and Phase Separation of Active Layers via Incorporating GHK-Cu.

Abstract

The crystallinity of a nonfullerene small-molecule acceptor plays an important function in the bimolecular recombination and carrier transfer of polymer solar cells (PSCs). However, because of the competition between the donor (PBDB-T) and acceptor (ITIC) in processes of phase separation and crystallization, the PBDB-T preferentially forms a crystalline network, which limits the molecular diffusion of ITIC and leads to the weak crystallinity of ITIC, eventually restricting the photoelectric conversion efficiency (PCE) of PSCs. Therefore, in our work, a small-molecule biomaterial, Gly-His-Lys-Cu (SMBM GHK-Cu), is incorporated into binary PBDB-T:ITIC to construct a PBDB-T:ITIC:GHK-Cu ternary system. The addition of GHK-Cu increases ITIC crystallinity and promotes the formation in continuous single-phase domains of PBDB-T and ITIC, which creates an optimized bicontinuous network path to increase and balance charge transmission in PSCs. Meanwhile, GHK-Cu makes energy transfer from GHK-Cu to PBDB-T appreciably efficient, improving the photon capture and exciton-generation rate of PBDB-T. Moreover, it can form a complementary absorption spectrum with PBDB-T and ITIC, which enhances the PCE of ternary devices. Excitingly, the PCE of PSC-based PBDB-T:ITIC is enhanced from 10.28% to 12.07% via incorporating 0.1 wt % GHK-Cu into PBDB-T:ITIC, in which the enhanced open voltage (VOC) is 0.92 V, the short-circuit current (JSC) is 17.87 mA/cm2, and the fill factor (FF) is 73.4%. Meanwhile, the PCE of PSC-based PM6:Y6 is also enhanced from 15.21% for a binary PSC to 17.11% for ternary PSC-based PM6:Y6:0.1 wt % GHK-Cu. This work shows that the cheap and environmentally friendly GHK-Cu has great potential for application in tuning the crystallinity and phase separation of the active layer.