Improving power conversion efficiency (PCE) is important for broadening the applications of organic photovoltaic (OPV) cells. Here, a maximum PCE of 19.0% (certified value of 18.7%) is achieved in single‐junction OPV cells by combining material design with a ternary blending strategy. An active layer comprising a new wide‐bandgap polymer donor named PBQx‐TF and a new low‐bandgap non‐fullerene acceptor (NFA) named eC9‐2Cl is rationally designed. With optimized light utilization, the resulting binary cell exhibits a good PCE of 17.7%. An NFA F‐BTA3 is then added to the active layer as a third component to simultaneously improve the photovoltaic parameters. The improved light unitization, cascaded energy level alignment, and enhanced intermolecular packing result in open‐circuit voltage of 0.879 V, short‐circuit current density of 26.7 mA cm−2, and fill factor of 0.809. This study demonstrates that further improvement of PCEs of high‐performance OPV cells requires fine tuning of the electronic structures and morphologies of the active layers.

As a promising strategy for enhancing light utilization, constructing cell with tandem structure exhibits great potential in achieving high efficiency, which encourages the field of organic solar cells. Here, we develop an advanced interconnecting layer for tandem organic solar cell, which is composed of electron beam evaporated TiO x and PEDOT:PSS. By using electron beam evaporation, a sharp, smooth, and dense TiO x /PEDOT:PSS interface is obtained. By exquisite controlling the O 2 flux during evaporation, efficient electron extraction and low Schottky barrier are obtained in PBDB-TF:GS-ISO/TiO 1.76 and TiO 1.76 /PEDOT:PSS, which guarantee the charge recombination between two subcells. The tandem cell with interconnecting layer of TiO 1.76 /PEDOT:PSS shows 20.27% efficiency, which is certified as 20.0% by National Institute of Metrology, China. Therefore, our result marks the arrival of 20% era in the field of organic solar cells.

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The development of organic photoactive materials, especially the newly emerging non-fullerene electron acceptors (NFAs), has enabled rapid progress in organic photovoltaic (OPV) cells in recent years. Although the power conversion efficiencies (PCEs) of the top-performance OPV cells have surpassed 16%, the devices are usually fabricated via a spin-coating method and are not suitable for large-area production. Here, we demonstrate that the fine-modification of the flexible side chains of NFAs can yield 17% PCE for OPV cells. More crucially, as the optimal NFA has a suitable solubility and thus a desirable morphology, the high efficiencies of spin-coated devices can be maintained when using scalable blade-coating processing technology. Our results suggest that optimization of the chemical structures of the OPV materials can improve device performance. This has great significance in larger-area production technologies that provide important scientific insights for the commercialization of OPV cells.

The advantage in low cost makes P3HT one of the most attractive electron donors for photovoltaic applications, but the power conversion efficiency (PCE) of the P3HT-based organic solar cells (OSCs)...

The development of polymerized small‐molecule acceptors has boosted the power conversion efficiencies (PCEs) of all‐polymer organic photovoltaic (OPV) cells to 17%. However, the polymer donors suitable for all‐polymer OPV cells are still lacking, restricting the further improvement of their PCEs. Herein, a new polymer donor named PQM‐Cl is designed and its photovoltaic performance is explored. The negative electrostatic potential and low average local ionization energy distribution of the PQM‐Cl surface enable efficient charge generation and transfer process. When blending with a well‐used polymer acceptor, PY‐IT, the PQM‐Cl‐based devices deliver an impressive PCE of 18.0% with a superior fill factor of 80.7%, both of which are the highest values for all‐polymer OPV cells. The relevant measurements demonstrate that PQM‐Cl‐based films possess excellent mechanical and flexible properties. As such, PQM‐Cl‐based flexible photovoltaic cells are fabricated and an excellent PCE of 16.5% with high mechanical stability is displayed. These results demonstrate that PQM‐Cl is a potential candidate for all‐polymer OPV cells and provide insights into the design of polymer donors for high‐efficient all‐polymer OPV cells.

Ternary organic solar cells are promising alternatives to the binary counterpart due to their potential in achieving high performance. Although a growing number of ternary organic solar cells are recently reported, less effort is devoted to morphology control. Here, ternary organic solar cells are fabricated using a wide-bandgap polymer PBT1-C as the donor, a crystalline fused-ring electron acceptor ITIC-2Cl, and an amorphous fullerene derivative indene-C bisadduct (ICBA) as the acceptor. It is found that ICBA can disturb π-π interactions of the crystalline ITIC-2Cl molecules in ternary blends and then help to form more uniform morphology. As a result, incorporation of 20% ICBA in the PBT1-C:ITIC-2Cl blend enables efficient charge dissociation, negligible bimolecular recombination, and balanced charge carrier mobilities. An impressive power conversion efficiency (PCE) of 13.4%, with a high fill factor (FF) of 76.8%, is eventually achieved, which represents one of the highest PCEs reported so far for organic solar cells. The results manifest that the adoption of amorphous fullerene acceptor is an effective approach to optimizing the ternary blend morphology and thereby increases the solar cell performance.

By constructing a ternary cell with a B1:BO-2Cl:BO-4Cl donor:acceptors combination, an outstanding power conversion efficiency (PCE) of 17.0% (certified to be 16.9%) has been realized for all-small-molecule organic solar cells (ASM-OSCs).