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Summary The growth of the internet of things (IoT) is creating a demand for convenient energy sources, like organic photovoltaics, to power various small IoT devices. Here, we report a highly crystalline small molecular acceptor (named FCC-Cl) with an optical band gap of 1.71 eV suitable for indoor applications. The important design rationale of FCC-Cl is the combination of a weak electron-donating core and a moderate electron-withdrawing end group, which leads to needed band gap and high crystallinity. The OPVs based on D18:FCC-Cl achieved a high external quantum efficiency up to 85% and a high fill factor of 80% due to the high absorption coefficient and strong crystallinity of FCC-Cl. Consequently, an impressive power conversion efficiency of 28.8% was achieved under a 2,600 K LED lamp at 500 lux. It was also demonstrated that PM6:FCC-Cl-based devices can achieve high efficiencies over a wide range of active-layer thicknesses, which is a feature necessary for large-scale roll-to-roll printing processes.

In this paper, we demonstrate a solution-processed MoSe2 quantum dots/PEDOT:PSS bilayer hole extraction layer (HEL) for non-fullerene organic solar cells (OSCs). It is found that the introduction of MoSe2 QDs can alter the work function and phase separation of PEDOT:PSS, thus affecting the morphology of the active layer and improving the performance of OSCs. The MoSe2 QDs/PEDOT:PSS bilayer HEL can improve the fill factor (FF), short-circuit current density (Jsc) and power conversion efficiency (PCE) of OSCs based on different active layers. The best PCE of up to 17.08% was achieved based on a recently reported active layer binary system named SZ2:N3, which is among the highest reported values to date for OSCs using 2D materials as an interface modifier. Our study indicates that this simple and solution-processed MoSe2 QDs/PEDOT:PSS bilayer thin film could be a potential alternative HEL to the commonly used PEDOT:PSS conducting polymers.

The field of organic solar cells has experienced paradigm-shifting changes in recent years because of the emergence of nonfullerene acceptors (NFAs). It is critically important to gain more insight...

Developing high-performance donor polymers is important for nonfullerene organic solar cells (NF-OSCs), as state-of-the-art nonfullerene acceptors can only perform well if they are coupled with a matching donor with suitable energy levels. However, there are very limited choices of donor polymers for NF-OSCs, and the most commonly used ones are polymers named PM6 and PM7, which suffer from several problems. First, the performance of these polymers (particularly PM7) relies on precise control of their molecular weights. Also, their optimal morphology is extremely sensitive to any structural modification. In this work, a family of donor polymers is developed based on a random polymerization strategy. These polymers can achieve well-controlled morphology and high-performance with a variety of chemical structures and molecular weights. The polymer donors are D-A1-D-A2-type random copolymers in which the D and A1 units are monomers originating from PM6 or PM7, while the A2 unit comprises an electron-deficient core flanked by two thiophene rings with branched alkyl chains. Consequently, multiple cases of highly efficient NF-OSCs are achieved with efficiencies between 16.0% and 17.1%. As the electron-deficient cores can be changed to many other structural units, the strategy can easily expand the choices of high-performance donor polymers for NF-OSCs.

Thiophene and its derivatives have been extensively used in organic electronics, particularly in the field of polymer solar cells (PSCs). Significant research efforts have been dedicated to modifying thiophene-based units by attaching electron-donating or withdrawing groups to tune the energy levels of conjugated materials. Herein, we report the design and synthesis of a novel thiophene derivative, FE-T, featuring a monothiophene functionalized with both an electron-withdrawing fluorine atom (F) and an ester group (E). The FE-T unit possesses distinctive advantages of both F and E groups, the synergistic effects of which enable significant downshifting of the energy levels and enhanced aggregation/crystallinity of the resulting organic materials. Shown in this work are a series of polymers obtained by incorporating the FE-T unit into a PM6 polymer to fine-tune the energetics and morphology of this high-performance PSC material. The optimal polymer in the series shows a downshifted HOMO and an improved morphology, leading to a high PCE of 16.4% with a small energy loss (0.53 eV) enabled by the reduced non-radiative energy loss (0.23 eV), which are among the best values reported for non-fullerene PSCs to date. This work shows that the FE-T unit is a promising building block to construct donor polymers for high-performance organic photovoltaic cells.