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The development of portable X‐ray detectors is necessary for diagnosing fractures in unconscious patients in emergency situations. However, this is quite challenging because of the heavy weight of the scintillator and silicon photodetectors. The weight and thickness of X‐ray detectors can be reduced by replacing the silicon layer with an organic photodetectors. This study presents a novel bithienopyrroledione‐based polymer donor that exhibits excellent photodetection properties even in a thick photoactive layer (~700 nm), owing to the symmetric backbone and highly soluble molecular structure of bithienopyrroledione. The ability of bithienopyrroledione‐based polymer donor to strongly suppress the dark current density (Jd ~ 10−10 A cm−2) at a negative bias (−2.0 V) while maintaining high responsivity (R = 0.29 A W−1) even at a thickness of 700 nm results in a maximum shot‐noise‐limited specific detectivity of Dsh* = 2.18 × 1013 Jones in the organic photodetectors. Printed organic photodetectors are developed by slot‐die coating for use in X‐ray detectors, which exhibit Dsh* = 2.73 × 1012 Jones with clear rising (0.26 s) and falling (0.29 s) response times upon X‐ray irradiation. Detection reliability is also proven by linear response of the X‐ray detector, and the X‐ray detection limit is 3 mA. [ABSTRACT FROM AUTHOR]

With the drive toward the development of large‐area organic solar cells (OSCs), there is a critical need for advanced fabrication techniques that ensure both their efficiency and scalability. In particular, a shift from toxic halogenated solvents to safer non‐halogenated alternatives such as o‐xylene, which have lower environmental and health impacts, is required. However, transitioning to non‐halogenated solvents can lead to serious problems, including aggregation within the active layer, which compromises film morphology and the resulting efficiency of OSCs. To address this aggregation, in the present study, the 2‐ethylhexyl (EH) groups in L8‐BO(EH‐EH) are replaced with longer chains (2‐heptylundecyl [HU], 2‐decyltetradecyl [DT], and 2‐dodecylhexadecyl [DH] groups) to synthesize the non‐fullerene acceptors (NFAs) of L8‐BO(HU‐HU), L8‐BO(HU‐DT), and L8‐BO(HU‐DH). The NFAs with the longer alkyl chains are highly soluble in o‐xylene and produce highly uniform films, making them more suitable for use in large‐area OSCs. Using the NFAs, slot‐die‐coated organic solar modules with an active area of 200 cm2 are fabricated; the L8‐BO(HU‐DT)‐based module exhibits an impressive power conversion efficiency of 11.44%. This work thus underscores the asymmetrical elongation of alkyl chains in the NFAs to mitigate severe NFA phase separation and improve film printability in the practical production of organic solar modules. [ABSTRACT FROM AUTHOR]

Photoelectrochemical (PEC) cells offer a promising method for producing green hydrogen through the splitting of water using solar energy. However, the cost‐effective synthesis of highly crystalline p‐type semiconductor materials for PEC cells remains a significant challenge for industrial applications. Herein, a CuInS2 photoelectrode is fabricated using a scalable and economical wet chemical spin‐coating technique. To enhance the crystallinity and photoelectrochemical activity of the photoelectrode, the grain size is precisely controlled by adjusting the atomic ratio, thickness, morphology, and Ag doping. Evaluating a novel growth mechanism of CuInS2 from Cu–In–O reveals that Ag doping significantly promotes grain growth. Consequently, the CuInS2 photocathode achieves one of the highest photoelectrochemical activities (−9.8 mA cm−2 at 0 VRHE) reported for CuInS2 photoelectrodes synthesized via wet chemical methods. Bias‐free water splitting is achieved using a CuInS2‐based photoelectrode in a photovoltaic–PEC cell configuration. These results highlight the potential of CuInS2, prepared through wet chemical methods, for cost‐effective photoelectrochemical water splitting. [ABSTRACT FROM AUTHOR]

The emergence of Y6 and its derivatives has significantly advanced organic photovoltaics (OPVs). However, the limited design strategies for Y6-based non-fullerene acceptors (NFAs) in absorbing visible light restrict their application in indoor OPVs (IOPVs). Furthermore, the reliance on additive-assisted chlorinated solvents for processing photoactive layers poses a significant barrier to IOPV commercialization. Herein, we synthesized two IPC-ended NFAs (IPC-BBO-IC2F and IPC-BBO-IC2Cl) and two IPC1CF3-ended NFAs (IPC1CF3-BBO-IC2F and IPC1CF3-BBO-IC2Cl). These asymmetric NFAs, featuring two distinct groups at the molecular ends, demonstrated blue-shifted absorption and elevated energy levels compared to Y6, offering a promising approach to harness indoor light and achieve higher open-circuit voltages more effectively. IOPVs processed without additives and using o-xylene, based on PM6:IPC1CF3-BBO-IC2F and PM6:IPC1CF3-BBO-IC2Cl, showed high efficiencies of 26.5% and 24.2%, respectively, under 1000-lux light-emitting diode (LED) illumination. These efficiencies surpass those of IOPVs that employ IPC-ended NFAs or Y6. Moreover, ternary IOPVs based on PM6:Y6:IPC1CF3-BBO-IC2F and PM6:Y6:IPC1CF3-BBO-IC2Cl achieved notable efficiencies of 26.9% and 27.1% under 1000 lux-LED illumination and 30.2% and 29.2% under 1000 lux-fluorescent light (FL) illumination, respectively. These findings underscore the potential of the IPC1CF3 end group in the asymmetric structural modification of Y6 to enhance the performance of IOPVs using additive-free and environmentally benign solvents. [ABSTRACT FROM AUTHOR]

Metal–organic frameworks (MOFs) have emerged as promising materials for triboelectric nanogenerators (TENGs), but the effects of ligand choice on triboelectric charge remain underexplored. Hence, this paper demonstrates the effect of single, binary, and ternary ligands on TENG performance of cobalt/cerium‐based (Co─Ce) bimetallic MOFs utilizing 2‐methylimidazole (2Melm), terephthalic acid (BDC), and benzene tricarboxylic acid (BTC) as ligands. The detailed structural characterization revealed that varying ligand chemistries led to distinct MOF features affecting TENG performance. Single ligand bimetallic MOFs (designated as CoCe‐2MeIm, CoCe‐BDC, CoCe‐BTC) has lower performance than binary ligand (designated as CoCe‐2MeIm‐BDC, CoCe‐2MeIm‐BTC, CoCe‐BDC‐BTC) and ternary ligand MOFs (designated as CoCe‐2MeIm‐BDC‐BTC). Among all, the binary ligand MOF, CoCe‐2MeIm‐BTC, shows the best results (598 V, 26.7 µA) due to the combined effect of imidazole ring and (─COO─) groups. This is attributed to lone pairs on nitrogen atoms and a delocalized π‐electron system in imidazole system in this material. CoCe‐BTC has the lowest results (31 V, 3.2 µA) due to the bulkier nature of the electron‐withdrawing (─COO─) groups and their impact on the π‐electron system of the benzene ring. This study showcases the potential of ligand chemistry manipulation to control triboelectric charge and thereby enhance MOF‐based TENG performance. [ABSTRACT FROM AUTHOR]

It remains challenging to fabricate efficient, scalable large-area organic solar cells (OSCs) owing to the unfavorable morphology of photoactive blend films. To address this challenge, two asymmetric nonfullerene acceptors (NFAs) IPC1CN-BBO-IC2F and IPC1CN-BBO-IC2Cl are synthesized, where 12,13-bis(2-butyloctyl)-3,9-diundecyl-12,13-dihydro-[1,2,5]thiadiazolo[3,4- e]thieno[2'",3'":4',5']thieno[2',3':4,5]pyrrolo[3,2-g]thieno[2',3':4,5]thieno-[3,2- b]indole (BBO) is the molecular core, and two types of end groups are appended to its ends, namely the 9H-indeno[1,2-fe]pyrazine-2,3,8-tricarbonitrile (IPC1CN) end group and one of 2-(5,6-dihalo-3-oxo-2,3-dihydro-1H-inden-1-ylidene)malononitrile end groups (IC2F or IC2Cl). These NFAs facilitate effective tuning of light absorption and energy levels, offer high carrier mobilities, and allow for the formation of appropriate morphologies. Note that these benefits apply even to large-area devices, unlike typical Y6-based NFAs. In addition, a random copolymer PM6-PBDBT(55) is synthesized and its energy levels are optimally matched with those of the asymmetric NFAs. The blade-coated 1 cm2-area OSCs based on PM6-PBDBT(55):IPC1CN-BBO-IC2Cl exhibit a PCE of 14.12%, which is higher than that of PM6-PBDBT(55)-IPC1CN-BBO-IC2F-based OSCs. More importantly, the PM6-PBDBT(55):IPC1CN-BBO-IC2Cl-based large-area (58.50 cm2) modules yield an impressive PCE of 11.28% with a small cell-to-module loss in fill factor. These results suggest that a combination of the asymmetric molecular design using the IPC1CN group and the terpolymer strategy will pave a new path for fabricating highly efficient and scalable large-area OSCs. [ABSTRACT FROM AUTHOR]

A low‐bandgap PBDTDTPD polymer is synthesized. It is a donor‐acceptor‐type polymer that consists of dialkylthiophenyl benzodithiophene (BDT) donor unit and N‐octyl‐2,7‐dithia‐5‐aza‐cyclopenta[a]pentalene‐4,6‐dione (DTPD) acceptor unit. The thienothiophene‐fused strong‐electron‐withdrawing DTPD effectively reduces the bandgap of the resulting polymer and keeps its highest occupied molecular orbital low. Moreover, PBDTDTPD is thermally stable and dissolves well in typical organic solvents. PBDTDTPD:PC71BM(1:1) blend film showed a power conversion efficiency of 3.18% and a largely elevated open‐circuit voltage of 0.75 V compared to that of well‐known P3HT:PC61BM blend film. In this work, we prove that the DTPD moiety can be utilized to develop a future low‐bandgap material that can absorb a broad wavelength of light and have high thermal stability, which are important characteristics for next‐generation high‐performance organic solar cells. [ABSTRACT FROM AUTHOR]

In this paper, we propose an ultrahigh‐resolution organic light‐emitting diodes (OLEDs) pixels patterned by conventional photolithography through by incorporating silicone into phosphorescent small‐molecule networks. This silicone‐integrated phosphorescent organic light‐emitting diode (SI‐phOLED), in which silicone molecules are homogeneously crosslinked with small‐molecule light‐emitting materials, can effortlessly achieve to 3,000 PPI ultrahigh‐resolution patterns using the photolithography process. [ABSTRACT FROM AUTHOR]

White light is attained by combining different‐colored emissions. White organic light‐emitting diodes, therefore, should be fabricated to obtain mixed emissions from different organic luminophores while suppressing energy transfer between each other. Here, the authors present a simple means to realize this goal by forming two‐color strip‐patterns of light‐emitting polymer (orange) and an iridium complex (sky‐blue) luminophores entirely through solution processes. The formation of the two‐color patterns is facilitated by i) the use of a highly efficient crosslinker permitting the construction of structurally robust orange primary strip‐patterns and ii) the contrast in the surface energy allowing selective wetting of the secondary sky‐blue patterns between the orange primary patterns. The emissive layer comprising the two‐color strip ‐patterns allows for the mixing ratio of the two colors to be adjusted by simply varying the areal ratio of the two patterns, which in turn, controls the white emission color‐temperature from 2119 to 7994 K. [ABSTRACT FROM AUTHOR]

The photovoltaic performance of inverted perovskite solar cells (PSCs) relies on effectively managing the interface between the hole extraction layer and the light‐absorbing perovskite layer. In this study, we have synthesised (4‐(3,6‐bis(methylthio)‐9H‐carbazol‐9‐yl)butyl)phosphonic acid (MeS‐4PACz), which forms a self‐assembled monolayer (SAM) on the fluorine‐doped tin oxide (FTO) electrode. The molecule‘s methylthio substituents generate a favourable interfacial dipole moment and interact with the perovskite layer. This interaction results in well‐aligned energy levels among the FTO/SAM/perovskite layers, promoting efficient hole extraction and significantly reducing carrier recombination losses. Additionally, the methylthio groups passivate iodide vacancies and interact with Pb2+ ions of the perovskite, reducing defect‐induced trap states and enhancing the crystalline growth of the perovskite layer. Consequently, inverted PSCs incorporating MeS‐4PACz achieve a power conversion efficiency of 25.13 %, along with outstanding photostability. [ABSTRACT FROM AUTHOR]

Organic optoelectronic devices that can be fabricated at low cost have attracted considerable attention because they can absorb light over a wide frequency range and have high conversion efficiency, as well as being lightweight and flexible. Moreover, their performance can be significantly affected by the choice of the charge-selective interlayer material. Nonstoichiometric nickel oxide (NiO x ) is an excellent material for the hole-transporting layer (HTL) of organic optoelectronic devices because of the good alignment of its valence band position with the highest occupied molecular orbital level of many p-type polymers. Herein, we report a simple low-temperature process for the synthesis of NiO x nanoparticles (NPs) that can be well dispersed in solution for long-term storage and easily used to form thin NiO x NP layers. NiO x NP-based organic photodiode (OPD) devices demonstrated high specific detectivity ( D *) values of 10 12 -10 13 jones under various light intensities and negative biases. The D * value of the NiO x NP-based OPD device was 4 times higher than that of a conventional poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS)-based device, an enhancement that originated mainly from the 16 times decreased leakage current. The NiO x NP-based OPD device demonstrated better reliability over a wide range of light intensities and operational biases in comparison to a device with a conventional sol-gel-processed NiO x film. More importantly, the NiO x NP-based OPD showed long-term device stability superior to those of the PEDOT:PSS and sol-gel-processed NiO x -based devices. We highlight that our low-temperature solution-processable NiO x NP-based HTL could become a crucial component in the fabrication of stable high-performance OPDs.