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.

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OSCs have mainly employed bulk heterojunction (BHJ) structures in the photoactive layers, in which the blend casting (BC) of donor (D) and acceptor (A) materials can form interpenetrating networks with a large D/A interface area for exciton dissociation. However, it is challenging to delicately balance the self-aggregation and miscibility of the two components during the one-step deposition, involving complicated dynamic and kinetic processes. [12] Accordingly, the photovoltaic performances of BC devices depend strongly on the conditions of host solvents, [13] blending ratio of D:A, [14][15][16][17][18] processing additives, [19][20][21][22] and post-treatment. [23] Thus, it is difficult to control the film morphologies, especially the D/A distribution in the vertical direction of BC films, [12] which is closely related to the charge transport and collection.To tailor vertical phase distribution efficiently, the two-step deposition of D and A materials in a sequence, namely, the sequential deposition (SD) method, is considered as an alternative to the BC process. [24][25][26][27][28][29][30][31][32][33] Since the deposition of D and A can be performed independently, the SD OSCs offer unique advantages, including a favored vertical phase distribution and improved film morphology, which provides sufficient D/A interface area, and direct transport pathways for charge carriers. [34][35][36] Obviously, it is beneficial to exciton dissociation and chargeThe variation of the vertical component distribution can significantly influence the photovoltaic performance of organic solar cells (OSCs), mainly due to its impact on exciton dissociation and charge-carrier transport and recombination. Herein, binary devices are fabricated via sequential deposition (SD) of D18 and L8-BO materials in a two-step process. Upon independently regulating the spin-coating speeds of each layer deposition, the optimal SD device shows a record power conversion efficiency (PCE) of 19.05% for binary singlejunction OSCs, much higher than that of the corresponding blend casting (BC) device (18.14%). Impressively, this strategy presents excellent universality in boosting the photovoltaic performance of SD devices, exemplified by several nonfullerene acceptor systems. The mechanism studies reveal that the SD device with preferred vertical components distribution possesses high crystallinity, efficient exciton splitting, low energy loss, and balanced charge transport, resulting in all-around enhancement of photovoltaic performances. This work provides a valuable approach for high-efficiency OSCs, shedding light on understanding the relationship between photovoltaic performance and vertical component distribution.

The Visual Object Tracking challenge VOT2019 is the seventh annual tracker benchmarking activity organized by the VOT initiative. Results of 81 trackers are presented; many are state-of-the-art trackers published at major computer vision conferences or in journals in the recent years. The evaluation included the standard VOT and other popular methodologies for short-term tracking analysis as well as the standard VOT methodology for long-term tracking analysis. The VOT2019 challenge was composed of five challenges focusing on different tracking domains: (i) VOT-ST2019 challenge focused on short-term tracking in RGB, (ii) VOT-RT2019 challenge focused on "real-time" shortterm tracking in RGB, (iii) VOT-LT2019 focused on longterm tracking namely coping with target disappearance and reappearance. Two new challenges have been introduced: (iv) VOT-RGBT2019 challenge focused on short-term tracking in RGB and thermal imagery and (v) VOT-RGBD2019 challenge focused on long-term tracking in RGB and depth imagery. The VOT-ST2019, VOT-RT2019 and VOT-LT2019 datasets were refreshed while new datasets were introduced for VOT-RGBT2019 and VOT-RGBD2019. The VOT toolkit has been updated to support both standard shortterm, long-term tracking and tracking with multi-channel imagery. Performance of the tested trackers typically by far exceeds standard baselines. The source code for most of the trackers is publicly available from the VOT page. The dataset, the evaluation kit and the results are publicly available at the challenge website 1 .

The ternary strategy, introducing a third component into a binary blend, opens a simple and promising avenue to improve the power conversion efficiency (PCE) of organic solar cells (OSCs). The judicious selection of an appropriate third component, without sacrificing the photocurrent and voltage output of the OSC, is of significant importance in ternary devices. Herein, highly efficient OSCs fabricated using a ternary approach are demonstrated, wherein a novel non‐fullerene acceptor L8‐BO‐F is designed and incorporated into the PM6:BTP‐eC9 blend. The three components show complementary absorption spectra and cascade energy alignment. L8‐BO‐F and BTP‐eC9 are found to form a homogeneous mixed phase, which improves the molecular packing of both the donor and acceptor materials, and optimizes the ternary blend morphology. Moreover, the addition of L8‐BO‐F into the binary blend suppresses the non‐radiative recombination, thus leading to a reduced voltage loss. Consequently, concurrent increases in open‐circuit voltage, short‐circuit current, and fill factor are realized, resulting in an unprecedented PCE of 18.66% (certified value of 18.2%), which represents the highest efficiency values reported for both single‐junction and tandem OSCs so far.

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.

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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).