No abstract

Organic photovoltaics (OPVs) have emerged as a promising renewable energy generation technology in past decades. However, the deep understanding of the details in exciton dissociation and carrier recombination in ternary organic solar cells (OSCs) is still lacking. Herein, a novel ternary OSC based on a PTB7‐Th:Y6:ITIC blend with a power conversion efficiency (PCE) enhancement of 29% is reported. A trade‐off is surprisingly found to exist between the exciton dissociation and carrier recombination process. The addition of nonfullerene acceptor Y6 in the ternary blend is found to create an efficient exciton dissociation process but accelerates the free carrier recombination process. Dielectric properties are also studied for ternary OSCs. The addition of Y6 into the binary blend is found to tune down the dielectric constant of the active layer and as a result accelerates the carrier recombination. The best performance is obtained for PTB7‐Th:Y6(5 wt%):ITIC(95 wt%)‐based ternary devices. In addition to its balanced charge carrier mobility and efficient charge extraction process, PTB7‐Th:Y6(5 wt%):ITIC(95 wt%)‐based ternary devices reach a balance in the trade‐off between the exciton dissociation and carrier recombination process and thus achieve the highest short‐circuit current density (Jsc) value.

Organic solar cells (OSCs) have again become a hot research topic in recent years. The record power conversion efficiency (PCE) of OSCs has boosted to over 17% in 2020. Apart from the high PCE, the stability of OSCs is also critical for their future applications and commercialization. Recently, many studies have proposed that burn-in degradation can be considered as an ineluctable barrier to long-term stable OSCs. However, there is still lack of studies to explain the detailed mechanism of this burn-in process. In this work, we first investigated the mechanism of the burn-in process in the high-efficiency PM6:N3-based nonfullerene OSCs. The PM6:N3-based device achieved a profound average PCE of 14.10% but also showed a significant performance loss after the burn-in degradation. Following characterizations such as dark J−V, photoluminescence (PL), time-resolved PL, Urbach energy estimation, and electrochemical impedance spectroscopy reveal that the burn-in degradation observed is closely related to the current extraction, energy transfer, nonradiative recombination, and charge transport process in the PM6:N3-based device. At the same time, it has small effects on the exciton dissociation process and energetic disorder in the PM6:N3-based device. Atomic force microscopy, scanning electron microscopy, transmission electron microscopy, and grazing incidence X-ray diffraction measurements gratifyingly found that the morphology of the PM6:N3 active layer is relatively stable during the burn-in degradation. Therefore, these observed degradations are suspected results from the instability of interfaces and electrodes. The atoms in carrier transport layers and electrodes may diffuse to the active layer during the degradation, which changes the energy levels of each layer and causes traps at the interface and in the active layer. Conquering the instability of interfaces and electrodes is proposed as the prior task for PM6:N3-based OSCs to achieve long-term stability. Our study provides insights into the mechanism behind the burn-in degradation of the PM6:N3-based OSCs, which takes the first step to conquer this barrier.

The inherently linear polypropylene suffers unsatisfying foaming behavior due to its low melt strength. To overcome this drawback, polypropylene‐/polypropylene‐grafted glycidyl methacrylate/thermoplastic polyester elastomer (PP/PP‐g‐GMA/TPEE) blending foam is prepared by the chemical foaming method in this study. The foaming mechanism of blending was studied from the aspects of the rheological behavior and the crystallization property. The results show that TPEE disperses in the PP matrix with fine particles and forms ideal interfaces, which provide a large number of nucleation sites for the foaming process of blending, inducing heterogeneous nucleation. Both of the 15 wt% and 20 wt% TPEE‐modified PP composites show higher shear viscosity and obvious strain hardening behavior. It has been proved that the cross‐linking network structure formed by TPEE and PP‐g‐GMA reaction improves the melt strength. The cell size decreases from 37.6 to 24.8 μm, and the cell density increases from 2.9 × 106 cells/cm3 to 2.5 × 107 cells/cm3. Compared with PP composites, the foaming window of the PP/PP‐g‐GMA/TPEE composites was widened.