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Two-dimensional (2D) Dion-Jacobson (DJ) perovskite solar cells (PSCs), despite their advantage in versatility of n-layer variation, are subject to poor photovoltaic efficiency, particularly in the fill factor (FF), compared to their three-dimensional counterparts. To enhance the performance of DJ PSCs, the process of growing crystals and hence the corresponding morphology of DJ perovskites are of prime importance. Herein, we report the fast nonisothermal (NIT) crystallization protocol that is previously unrecognized for 2D perovskites to significantly improve the morphology, orientation, and charge transport of the DJ perovskite films. Comprehensive mechanistic studies reveal that the NIT effect leads to the secondary crystallization stage, forming network-like channels that play a vital role in the FF's leap-forward improvement and hence the DJ PSC's performance. As a whole, the NIT crystallized PSCs demonstrate a high power conversion efficiency and an FF of up to 19.87 and 86.16%, respectively. This research thus provides new perspectives to achieve highly efficient DJ PSCs.

Efficient control of the perovskite crystallization and passivation of the defects at the surface and grain boundaries of perovskite films have turned into the most important strategies to restrain charge recombination toward high-performance and long-term stability of perovskite solar cells (PSCs). In this paper, we employed a small amount of natural vitamin B (carnitine) with dual functional groups in the MAPbI3 precursor solution to simultaneously passivate the positive- and negative-charged ionic defects, which would be beneficial for charge transport in the PSCs. In addition, such methodology can efficiently ameliorate crystallinity with texture, better film morphology, high surface coverage, and longer charge carrier lifetime, as well as induce preferable energy level alignment. Benefiting from these advantages, the power conversion efficiency of PSCs significantly increases from 16.43 to 20.12% along with not only a higher open-circuit voltage of 1.12 V but also an outstanding fill factor of 82.78%.

Inverted perovskite solar cells (PSCs) have attracted intense attention because of their insignificant hysteresis and low-temperature fabrication process. However, the efficiencies of inverted PSCs are still inferior to those of commercialized silicon solar cells. Also, the poor stability of PSCs is one of the major impedances to commercialization. Herein, we rationally designed and synthesized a new series of electron donor (

A series of tailor-made highly efficient and near-infrared (NIR) porphyrin-based acceptors is designed and synthesized for fullerene-free bulk-heterojunction (BHJ) organic solar cells. Constructing BHJ active layers using a PTB7-Th donor and porphyrin acceptors (P-x), which have complementary absorption, accomplishes panchromatic photon-to-current conversion from 300 to 950 nm. Our study shows that side chains of the porphyrin acceptors fairly influence the molecular ordering and nanomorphology of the BHJ active layers. Significantly, the porphyrin acceptor with four dodecoxyl side chains (P-2) achieves an open-circuit voltage (VOC) of 0.80 V, short-circuit current density (JSC) of 13.94 mA cm-2, fill factor of 64.8%, and overall power conversion efficiency of 7.23%. This great performance is attributable to the ascendant light-harvesting capability in the visible and near-infrared region, a high-lying LUMO energy level, a relatively high and more balanced carrier mobilities, and more ordered face-on molecular packing, which is beneficial for obtaining high VOC and JSC.

Two new asymmetric D−π−A1−A2 configured small molecules named PTP and TTP bearing thieno[3,4-b]pyrazine (TP) unit as the A1 group have been designed and synthesized for solution-processed bulk-heterojunction organic solar cells (OSCs). These new dipolar molecular donors not only exhibit strong near-IR absorption but pack into antiparallel dimers, in which PTP shows a coexistence of coplanar and cofacial antiparallel dimers configuration, while TTP reveals a coplanar centrosymmetric dimer structure. Solution-processed OSCs for PTP blended with pristine C70 achieves a promising power conversion efficiency (PCE) of 3.40% along with an open-circuit voltage (VOC) of 0.64 V, a short-circuit current density (JSC) of 9.83 mA cm−2 and a fill factor (FF) of 54.0%, which is the highest efficiency to date among the TP-based materials. Conversely, the optimized TTP:C70 solar cell delivers a VOC of 0.48 V, a JSC of 6.02 mA cm−2 and a FF of 43.3%, corresponding to a moderate PCE of 1.25%.

Detection of blood clotting by ultrasound has been widely explored. Many ultrasonic quantitative parameters have been demonstrated to have the ability to characterize clot. This study proposes the ultrasound Nakagami image as a tool to visually characterize the properties of blood clot. Whole blood samples with a hematocrit of 40% were made. A 10-mL whole blood was placed in a tube and 1 mL of 0.2 mol/L CaCl2 solution was added to induce clotting. A 35-MHz focused transducer was used to scan the tube filled with blood before and after blood clot formation for Nakagami imaging. The results showed that whole blood and clot have similar textures in their B-scans, but the Nakagami image behaved well in distinguishing between blood and clot. The Nakagami image before clot formation is based on red-blue-interlaced shading, corresponding to Rayleigh distribution (the Nakagami parameter m approaches 1). However, the clot has more blue shadings in the Nakagami image, representing that the backscattered statistics ...