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The fabrication of the flexible devices with excellent photovoltaic performance and stability is critical for the commercialization of organic solar cells (OSCs). Herein, the conjugated dimer acceptor DY‐TVCl and the non‐conjugated dimer acceptor DY‐3T based on the monomer MY‐BO are synthesized to regulate the molecular glass transition temperatures (Tg) for improving the morphology stability of active layer films. And the crack onset strain values for the blend films based on dimer acceptors are superior than that of small molecule, which are beneficial for the preparation of flexible devices. Accordingly, the binary device based on PM6:DY‐TVCl achieves a maximum power conversion efficiency (PCE) of 18.01%. Meanwhile, the extrapolated T80 (time to reach 80% of initial PCE) lifetimes of the PM6:DY‐TVCl‐based device and PM6:DY‐3T‐based device are 3091 and 2227 h under 1‐sun illumination, respectively, which are better than that of the PM6:MY‐BO‐based device (809 h). Furthermore, the flexible devices based on DY‐TVCl and DY‐3T exhibit the efficiencies of 15.23% and 14.34%, respectively. This work affords a valid approach to improve the stability and mechanical robustness of OSCs, as well as ensuring the reproducibility of organic semiconductors during mass production. [ABSTRACT FROM AUTHOR]

Gallium oxide (Ga2O3), with an ultrawide bandgap corresponding to the deep ultraviolet (DUV) range, has attracted significant attention in optical filter‐free photodetectors. In practical terms, DUV photodetectors employed in extreme conditions, for example, flame detection and space exploration, face the challenges of performance degradation caused by high/low‐temperature transformation. Here, DUV photodetectors are tailored with high durability and stability by one‐step‐grown β‐Ga2O3 films via pulsed laser deposition. A high‐oxygen‐pressure scheme effectively addresses the issue of film‐free deposition at specifically high temperatures, facilitating the formation of polycrystalline high‐resistivity β‐Ga2O3 films. As a result, the devices exhibit outstanding performance, including a low dark current (4.4 pA @30 V), high photoresponsivity (147.36 A W−1), and fast response time (3.1/22.6 ms). Additionally, the photoresponse performance shows minimal degradation at high temperatures up to 300 °C and even improves at low temperatures down to −100 °C, ranking it among the most robust DUV photodetectors. The mechanism of photoresponse, involving the exciton formation, bandgap evolution, carrier‐phonon scatter, etc., is also elucidated in a wide temperature range. This work provides an efficient solution for developing robust Ga2O3 DUV photodetectors with excellent performance for extreme‐condition applications. [ABSTRACT FROM AUTHOR]

The work presented an electrochemical anode method with different electrolyte concentrations and heat posttreatment to control the stoichiometry and structure of Cu2−xS electrocatalysts. X‐ray diffraction, X‐ray photoelectron spectroscopy, and scanning electron microscopy were employed to characterize the composition and morphology, whereas the electrocatalytic activity was evaluated by linear scanning voltammetry and electrochemical impedance spectroscopy. The results showed that the electrochemical method successfully synthesized thin flake‐shaped Cu7S4, which exhibited optimal performance at the electrolyte concentration of 0.45 mol L1 with maximum turnover frequency of 0.786 s−1, maximum mass activity of 0.539 A g−1, minimum charge transfer resistance of 0.156 Ω cm−2, and minimum overpotential of 154 mV at a current density of 10 mA cm−2. In the Cu7S4 structure, Cu2+ and S2− were coordinated in a CuS4 tetrahedral structure, whereas Cu+ and S2− were coordinated in a CuS3 triangular structure. Heat posttreatment could change the stoichiometry from 1.75 to 1.8 and improve the electrochemical performance. In the Cu9S5 structure, the CuS3 triangular structure had disappeared. Under the same conditions, the overvoltage was only 128 mV. [ABSTRACT FROM AUTHOR]

Comprehensive Summary: As the third generation new battery, the power conversion efficiency (PCE) of metal halide perovskite solar cells (PSCs) has increased from 3.8% in 2009 to 25.8% currently certified, which fully shows that they have great research value and development prospect. As one of the main components of high‐efficiency PSCs, hole transport materials (HTMs) play an important role in extracting and transporting holes and inhibiting charge recombination. However, commonly used HTMs require doping, and the hygroscopicity and corrosiveness of the dopants will destroy the stability of PSCs and hinder their commercialization. Therefore, it is of great significance to develop dopant‐free HTMs. In this review, the dopant‐free HTMs in recent six years are reviewed and summarized systematically, including organic small molecules, polymers and cross‐linkable materials. We focus on the design of the molecular cores and discuss their structure–property correlation, conductivity, and photovoltaic performance. Finally, how to design an ideal HTM is summarized. We hope that this review can provide reference for the development of low‐cost and dopant‐free HTMs to prepare efficient and stable PSCs. [ABSTRACT FROM AUTHOR]

In this study, a heterotrophic/biofilm‐electrode autotrophic denitrification reactor (HAD‐BER) was constructed and nano‐ɑ‐Fe2O3 was coated on granular activated carbon (GAC) as a third electrode to enhance the nitrate removal performance. The introduction of nano‐ɑ‐Fe2O3 could stimulate microorganisms to secrete more extracellular polymeric substances (EPS), accelerating the electron transfer. Moreover, more denitrification bacteria were enriched on the particle electrodes, especially Pseudomonas and Thermomonas, which played a significant role in denitrification. The denitrification performance at different COD/N ratios (0.65–3.23) and current intensities (0–150 mA) was investigated in depth. When the nitrate concentration of the influent was 60 mg/L, nitrate was almost completely removed at the optimal current intensity (60 mA) and COD/N ratio (1.29). At the same time, there was almost no nitrite (<0.10 mg/L) and ammonia nitrogen (0 mg/L) accumulation in the effluent. This study provided a new direction for the advancement of HAD‐BER and accelerated its implementation. Practitioner Points: By introducing nano‐a‐Fe2O3 into HAD‐BER, more denitrification bacteria were enriched on the particle electrodes.The increased contents of polysaccharide and protein content could accelerate the electron transfer.Almost completely denitrification could be achieved at current = 60 mA and COD/N = 1.29.The study provided a new direction for the further development of HAD‐BERs. [ABSTRACT FROM AUTHOR]

Wine‐processed Angelica Sinensis is a widely used Chinese medicinal decoction piece in China. However, there are hardly any robust markers indicating the processing procedure of wine‐processed Angelica Sinensis, including the amount of rice wine and processing degree. A strategy integrating untargeted metabolomics and chemometric analysis for deducing robust markers was provided and applied to the discrimination of processing procedure. First, 86 compounds were tentatively identified in wine‐processed Angelica Sinensis by ultra‐high‐performance liquid chromatography coupled with quadrupole‐time of flight mass spectrometry. Second, 93 potential chemical markers were selected using multivariate analysis, among which nine robust chemical markers were selected by verification with commercial samples. Finally, the effects of processing temperature, time, and amount of rice wine on the three selected chemical markers were investigated through a rapid analytical method. It was demonstrated that both m/z 258.1097 and 238.1189 were positively correlated with the amount of rice wine and processing degree. In summary, this study introduced two candidate processing markers as robust markers for discriminating the processing procedures of wine‐processed Angelica sinensis. It also proposed a strategy to provide the reference for the research of other decoction pieces. [ABSTRACT FROM AUTHOR]

Fish coloration, evolved from selection and adaptation, is a prominent feature of remarkable aquaculture merits. Fish possess more pigment cell types than any other vertebrates and are an excellent model for the study of mechanisms underlying skin coloration and pigmentation at levels from molecular genetics to system biology. How to effectively improve skin colour in ornamental and aquaculture fish has long been a focus on selective breeding programmes. In this review article, we introduce different types of chromatophore and early development of pigmentation, describe cellular mechanisms related to morphological and physiological changes of body colour and demonstrate applications of single‐sex control and molecular marker–assisted breeding in body colour selection. We also reviewed genes that have been found involving in neural crest migration and development, as well as those involved in melanin‐based coloration and other types of pigmentation, and explored how to use transgenic technology for enhancing fish body colour. The applications of genome editing and other omics technologies in relation to fish coloration are also illustrated. Finally, we present our perspectives about future fish coloration research and practice in aquaculture. Taken together, this review is expected to provide an update on cellular and molecular mechanisms in fish coloration and pigmentation, which will likely promote body colour–based molecular breeding programmes in aquaculture. [ABSTRACT FROM AUTHOR]

The cover image is based on the Review Article Fish pigmentation and coloration: molecular mechanisms and aquaculture perspectives by Zaijie Dong et al., https://doi.org/10.1111/raq.12583. [ABSTRACT FROM AUTHOR]

The excessive electric field gives rise to droplet non‐coalescence and droplet chains in the electric dehydrator, which severely deteriorates oil–water separation efficiency and even leads to short circuit. To reveal the underlying mechanism of droplet non‐coalescence, dynamic behavior of two neutral droplets in silicone oil under a direct current electric field is investigated by using high‐speed photography. The experimental results show that there exists a critical electric field strength above which two droplets will bounce off after the contact. The critical electric field strength of droplet non‐coalescence is affected by the initial separation distance between droplets, the radius of droplet, and the surfactant concentration. Whether the non‐coalescence behavior occurs in the electric field is determined by the competition of electric force and capillary force, which dominates the evolution of tiny connection channel. [ABSTRACT FROM AUTHOR]

Comprehensive Summary: As the third generation new battery, the power conversion efficiency (PCE) of metal halide perovskite solar cells (PSCs) has increased from 3.8% in 2009 to 25.8% currently certified, which fully shows that they have great research value and development prospect. As one of the main components of high‐efficiency PSCs, hole transport materials (HTMs) play an important role in extracting and transporting holes and inhibiting charge recombination. However, commonly used HTMs require doping, and the hygroscopicity and corrosiveness of the dopants will destroy the stability of PSCs and hinder their commercialization. Therefore, it is of great significance to develop dopant‐free HTMs. In this review, the dopant‐free HTMs in recent six years are reviewed and summarized systematically, including organic small molecules, polymers and cross‐linkable materials. We focus on the design of the molecular cores and discuss their structure–property correlation, conductivity, and photovoltaic performance. Finally, how to design an ideal HTM is summarized. We hope that this review can provide reference for the development of low‐cost and dopant‐free HTMs to prepare efficient and stable PSCs. [ABSTRACT FROM AUTHOR]