Herein we report the synthesis of a novel A-D-A-D-A non-fullerene small-molecule acceptor (NFSMA) bearing a diketopyrrolopyrrole (DPP) acceptor central core coupled to terminal rhodanine acceptors via a thiophene donor linker (denoted as MPU1) for use in non-fullerene polymer solar cells (PSCs). This NFSMA exhibits a narrow optical band gap (1.48 eV), strong absorption in the 600-800 nm wavelength region of the solar spectrum, and a lowest unoccupied energy level of -3.99 eV. When the mixture of a medium band gap D-A copolymer P (1.75 eV) was used as donor and MPU1 as acceptor, the blend film showed a broad absorption profile from 400 to 850 nm, beneficial for light harvesting efficiency of the resulted polymer solar cell. After optimization of the donor-to-acceptor weight ratios and concentration of solvent additive, the P-MPU1-based PSC exhibited a power conversion efficiency of 7.52% (J= 12.37 mA/cm, V = 0.98 V, and fill factor = 0.62), which is much higher than that for a P3HT-MPU1-based device (2.16%) prepared under identical conditions. The higher value for the P-MPU1-based device relative to the P3HT-MPU1-based one is related to the low energy loss and more balanced charge transport in the device based on the P donor. These results indicate that alteration of the absorption spectra and electrochemical energy levels of non-fullerene acceptors, and appropriate selection of the polymer donor with complementary absorption profile, is a promising means to further boost the performance of PSCs.

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Donor–acceptor–acceptor (D–A–A) type 1,8-naphthalimide based small molecules SM1 and SM2 functionalized with tetracyanobutadiene (TCBD) and dicyanoquino-dimethane (DCNQ) modules, showing strong absorption in the visible and near-infrared (NIR) region are reported.

Two small molecules composed of 1,1,4,4-tetracyanobuta-1,3-diene substituted diketopyrrolopyrroles (DPPs) denoted as DPP5 and DPP6 were synthesized and their photophysical and electrochemical properties were investigated. The frontier molecular orbitals based on empirical relation between cyclic voltammetry redox potentials, experimental IP, and EA energies indicate that these two small molecules can be used as an electron acceptor for the polymer bulk heterojunction solar cells. The BHJ solar cells combined with a low band gap D–A copolymer P as an electron donor exhibits promising power conversion efficiency of 3.90% and 4.95%, with DPP5 and DPP6, respectively, after the optimization of active layers, indicating that these small molecules based on DPPs can be the alternative as an electron acceptor to replace fullerene, leading to the low-cost solution-processed polymer solar cells.

Hybrid organic/inorganic perovskites are promising candidate materials for use in photovoltaic applications. More recently, they have also become highly attractive as active materials for other optoelectronic devices, including lasers, light-emitting diodes, and photodetectors. Nevertheless, difficulties in forming continuous and uniform films and the existence of a charge-injection barrier between the perovskite layer and the electrodes have hindered the development of high-performance perovskite light-emitting diodes (PeLEDs). In this study, a cross-linked hole-transport layer (HTL) is introduced to improve the hole-injection efficiency of PeLEDs. Furthermore, this layer simultaneously facilitates the formation of smooth perovskite layers, presumably because of the different surface energies. More interestingly, the HTL also exhibits strong solvent effects on the device performance. When the processing solvent for fabricating the HTLs is changed from chlorobenzene to N,N-dimethylformamide (DMF), the perovskite layer becomes more uniform and continuous, leading to better surface coverage and higher device efficiency, presumably because DMF has strong affinity toward the perovskite precursors. The approach presented herein could become a general method for decreasing the hole-injection barrier of PeLEDs and, eventually, lead to higher device performance.

Non-fullerene molecular acceptors in combination with a polymeric donor gave well performing BHJSCs with energy losses below 0.4 eV concomitant with outstanding external quantum efficiencies in the NIR-regime.

Two D–A copolymers, F1 and F2, with fluorene and thiazole units were substituted, respectively, on a thiadiazoloquinoxaline (TDQ) unit to enhance the electron-accepting strength of TDQ.

Herein, we investigated the photovoltaic properties of carbazole-based diketopyrrolopyrroles with tetracyanobutadiene acceptor units as highly efficient non-fullerene acceptors together with a D–A conjugated polymer, P, as a donor for polymer solar cells.