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None-fullerene solar cells with ternary architecture have attracted much attention because it is an effective approach for boosting the device power conversion efficiency. Here, the crystalline polymer N2200 as the third component is integrated into J71:ITIC bulk heterojunction. A series of characterizations indicate that N2200 could increase photo-harvesting, balanced hole and electron mobilities, enhanced exciton dissociation, and suppressed charge recombination, which result in the comprehensive improvement of open circuit voltage, short circuit current and fill factor in the device. Moreover, after introduction of N2200, the morphology of the ternary active layer is optimized, and the film crystallinity is improved. This work demonstrates that adding a small quantity of high crystallization acceptor into non-fullerene donor: acceptor mixture is a promising strategy toward developing high-performance organic solar cells. Image 1 • The effect of the crystalline polymer N2200 as the third component into J71:ITIC bulk heterojunction was investigated. • The enhanced device efficiency was attributed to balanced charge mobilities, and enhanced exciton dissociation. • The morphology and crystallization of the ternary active layer were optimized. [ABSTRACT FROM AUTHOR]

Abstract Interfacial compatibility between the electrode and organic semiconductor plays a critical role in controlling the charge transport and hence efficiency of organic solar cell. Here, we introduce a novel small-molecule zwitterionic electrolyte (S1) combined with ZnO as electron transporting interlayer employed for the inverted PTB7:PC 71 BM bulk heterojunction solar cell. The resulting device with the S1/ZnO stacked interlayer achieves a high PCE of 8.59%, obtaining a 16.2% improvement over the control device performance of 7.4% without the S1 attributed to the significant increased short-circuit current density and fill factor. The interfacial properties are investigated. It is found that the S1/ZnO interlayer possess an ultralow work function of 3.6 eV, which originates from the interfacial double dipole step induced by the zwitterionic side chain electrostatic realignment at interface. The S1/ZnO interlayer exhibits the excellent charge extraction ability, suppresses the charge recombination loss and decreases the series resistance at the active layer/electrode contact. Graphical abstract Image 1 Highlights • S1 coated ZnO layer is employed as electron transporting layer for inverted organic solar cell. • S1/ZnO stacked interlayer exhibits the excellent charge extraction ability. • ZnO/S1 stacked interlayer has an ultralow work function of 3.6 eV. • The efficiency of the device with the S1/ZnO interlayer constitutes a 16.2% improvement over that of the controlled device. [ABSTRACT FROM AUTHOR]