Excessive Aggregation Research Articles

Whole milk protein powder separated by low-temperature nanofiltration membrane administration alleviates sepsis-induced myopathy

Sepsis-induced myopathy (SIM) has been recognized as a critical risk factor for the development of acquired muscle weakness among patients in the intensive care unit. These individuals frequently encounter inadequate dietary intake and malnutrition. With the aggravation of the severity of the person’s condition, leading to increased skeletal muscle protein breakdown and reduced synthesis, which is an urgent problem to be solved in clinical nutritional treatment. Whole milk protein powder (WMPP) has promising bioactive nutrients and holds promising potential for enhancing skeletal muscle mass. The study was designed to delve into the potential effects and mechanisms of WMPP intervention for increaseing skeletal muscle mass on SIM mice. Our results clearly show that the intervention with WMPP can significantly improve the exercise capacity and skeletal muscle mass in SIM mice. It significantly increases the diameter and cross-sectional area (CSA) of skeletal muscle fibers, while effectively reducing the excessive aggregation of collagen fibers and the abnormal accumulation of adipose tissue in the skeletal muscle of SIM mice. Moreover, WMPP intervention also significantly alleviated the oxidative stress status of mitochondria, which subsequently enhanced the expression of mitochondrial metabolic enzymes. The mechanism may be associated with decreased AMPK phosphorylation in skeletal muscle tissue and simultaneously increased phosphorylation of mTOR, p70S6K1, and 4EBP-1 in SIM mice. In summary, the WMPP intervention significantly enhances exercise capacity and skeletal muscle mass while mitigating the oxidative stress status of mitochondria. Furthermore, it regulates skeletal muscle anabolism via the AMPK/mTOR signaling pathway in SIM mice.

Biomass‐Derived Carbon Materials for Smart Electronics: Insights from Wood Pitch‐based Microsupercapacitors

AbstractWood pitch, derived from dry distillation of wood, is a promising carbon electrode material. A novel strategy is presented for fabricating honeycomb‐like porous carbon nanosheets using a template‐free approach. Wood pitch is pre‐treated with H₂O₂ to introduce oxygen‐containing functional groups selectively at the edges of polycyclic aromatic hydrocarbons, enhancing hydrophilicity and reactivity. Adding rosin groups to the oxidized wood pitch molecules helps to regulate intermolecular spacing and prevent excessive aggregation, facilitating subsequent KOH intercalation activation and the formation of a porous structure. The resulting rosin‐modified wood pitch‐based carbon material (RWPC‐0.2) features a high specific surface area (3521.5 m2 g−1). With a current density of 1 A g−1, the device has a specific capacitance of 376 F g−1. After 5000 cycles at 10 A g−1, it still has 83.8% of its initial specific capacitance. Using direct ink writing (DIW) technology in combination with poly(3,4‐ethylenedioxythiophene): polystyrene sulfonate/RWPC‐0.2 (PEDOT: PSS/RWPC‐0.2) as the electrode ink, microelectrodes are fabricated and microsupercapacitors are constructed with high areal capacitance (460 mF cm−2), excellent rate performance, and good cycling stability. This study offers new insights for developing printed micro‐energy storage devices based on wood pitch‐derived carbon materials and opens new possibilities for the application of biomass materials in smart electronics.

Potential cardiac-derived exosomal miRNAs involved in cardiac healing and remodeling after myocardial ischemia–reperfusion injury

Migratory cells exist in the heart, such as immune cells, fibroblasts, endothelial cells, etc. During myocardium injury, such as ischemia–reperfusion (MIRI), cells migrate to the site of injury to perform repair functions. However, excessive aggregation of these cells may exacerbate damage to the structure and function of the heart, such as acute myocarditis and myocardial fibrosis. Myocardial injury releases exosomes, which are a type of vesicle with signal transduction function and the miRNA carried by exosomes can control cell migration function. Therefore, regulating this migratory cell population through cardiac-derived exosomal miRNA is crucial for protecting and maintaining cardiac function. Through whole transcriptome RNA sequencing, exosomal miRNA sequencing and single-cell dataset analysis, we (1) determined the potential molecular regulatory role of the lncRNA‒miRNA‒mRNA axis in MIRI, (2) screened four important exosomal miRNAs that could be released by cardiac tissue, and (3) screened seven genes related to cell locomotion that are regulated by four miRNAs, among which Tradd and Ephb6 may be specific for promoting migration of different cells of myocardial tissue in myocardial infarct. We generated a core miRNA‒mRNA network based on the functions of the target genes, which may be not only a target for cardiac repair but also a potential diagnostic marker for interactions between the heart and other tissues or organs. In conclusion, we elucidated the potential mechanism of MIRI in cardiac remodeling from the perspective of cell migration, and inhibition of cellular overmigration based on this network may provide new therapeutic targets for MIRI and to prevent MIRI from developing into other diseases.

Immp2l Deficiency Induced Granulosa Cell Senescence Through STAT1/ATF4 Mediated UPRmt and STAT1/(ATF4)/HIF1α/BNIP3 Mediated Mitophagy: Prevented by Enocyanin.

Dysfunctional mitochondria producing excessive ROS are the main factors that cause ovarian aging. Immp2l deficiency causes mitochondrial dysfunction and excessive ROS production, leading to ovarian aging, which is attributed to granulosa cell senescence. The pathway controlling mitochondrial proteostasis and mitochondrial homeostasis of the UPRmt and mitophagy are closely related with the ROS and cell senescence. Our results suggest that Immp2l knockout led to granulosa cell senescence, and enocyanin treatment alleviated Immp2l deficiency-induced granulosa cell senescence, which was accompanied by improvements in mitochondrial function and reduced ROS levels. Interestingly, redox-related protein modifications, including S-glutathionylation and S-nitrosylation, were markedly increased in Immp2l-knockout granulosa cells, and were markedly reduced by enocyanin treatment. Furthermore, STAT1 was significantly increased in Immp2l-knockout granulosa cells and reduced by enocyanin treatment. The co-IP results suggest that the expression of STAT1 was controlled by S-glutathionylation and S-nitrosylation, but not phosphorylation. The UPRmt was impaired in Immp2l-deficient granulosa cells, and unfolded and misfolded proteins aggregated in mitochondria. Then, the HIF1α/BNIP3-mediated mitophagy pathway was activated, but mitophagy was impaired due to the reduced fusion of mitophagosomes and lysosomes. The excessive aggregation of mitochondria increased ROS production, leading to senescence. Hence, Enocyanin treatment alleviated granulosa cell senescence through STAT1/ATF4-mediated UPRmt and STAT1/(ATF4)/HIF1α/BNIP3-mediated mitophagy.

Culinary properties, nutritional quality, and in vitro starch digestibility of innovative gluten-free and climate smart cowpea-based pasta

This study investigates the processability, culinary and rheological properties, biochemical composition and in-vitro starch digestibility of new gluten-free pasta formulated with whole cowpea flour alone or combined with teff and/or amaranth leaf flour(s). These pasta are compared with three wheat-based pasta with fiber content increasing from 4% to 16% g/100g, 16% g/100g being the average fiber content of cowpea-based pasta. The pasta were processed using low temperature extrusion and drying. The antioxidant properties of amaranth leaf flour facilitated extrusion by limiting excessive aggregation of the dough during hydration/mixing that is attributed to lipoxygenase activity of cowpea flour. The optimal cooking time and cooking losses of cowpea-based pasta were similar to wheat-based pasta with comparable fiber content, highlighting fiber as a key factor influencing culinary properties. Adding teff to cowpea-based pasta reduced cooking losses and firmness. Although some micronutrients were lost during pasta processing and cooking, the consumption of a cooked portion of 100 g of dry cowpea-based pasta still covered FAO nutritional recommendations for protein, fiber, iron, zinc, and vitamin B9 targeting adult women. Adding amaranth leaves helped meet recommended beta-carotene levels. The in vitro slowly digestible starch content of cowpea-based pasta is similar to or higher than that of wheat-based pasta.

Constraining the Excessive Aggregation of Non-Fullerene Acceptor Molecules Enables Organic Solar Modules with the Efficiency >16.

Translating high-performance organic solar cell (OSC) materials from spin-coating to scalable processing is imperative for advancing organic photovoltaics. For bridging the gap between laboratory research and industrialization, it is essential to understand the structural formation dynamics within the photoactive layer during printing processes. In this study, two typical printing-compatible solvents in the doctor-blading process are employed to explore the intricate mechanisms governing the thin-film formation in the state-of-the-art photovoltaic system PM6:L8-BO. Our findings highlight the synergistic influence of both the donor polymer PM6 and the solvent with a high boiling point on the structural dynamics of L8-BO within the photoactive layer, significantly influencing its morphological properties. The optimized processing strategy effectively suppresses the excessive aggregation of L8-BO during the slow drying process in doctor-blading, enhancing thin-film crystallization with preferential molecular orientation. These improvements facilitate more efficient charge transport, suppress thin-film defects and charge recombination, and finally enhance the upscaling potential. Consequently, the optimized PM6:L8-BO OSCs demonstrate power conversion efficiencies of 18.42% in small-area devices (0.064 cm2) and 16.02% in modules (11.70 cm2), respectively. Overall, this research provides valuable insights into the interplay among thin-film formation kinetics, structure dynamics, and device performance in scalable processing.

The natural flavonoid pinocembrin shows antithrombotic activity and suppresses septic thrombosis

Sepsis, an extreme host response to systemic infection, remains one of the leading causes of mortality worldwide. Platelets, which are integral to both thrombosis and inflammation, play a crucial role in the pathophysiology of sepsis. Excessive platelet activation and aggregation significantly increase the risk of thrombosis, thereby elevating mortality in septic patients. However, the etiology and treatment of this condition have not been comprehensively studied. This study identifies pinocembrin, a natural flavonoid compound derived from propolis, as a potential therapeutic agent for mitigating platelet activation and treating sepsis. In vivo, pinocembrin effectively inhibited FeCl3-induced carotid arterial occlusive thrombus formation and collagen/epinephrine-induced pulmonary thromboembolism in mouse models. In vitro, pinocembrin treatment suppressed multiple facets of platelet activation, including aggregation, secretion, and αIIbβ3-mediated signaling events. Mechanistically, pinocembrin repressed platelet functions by inhibiting Src/Syk/PLCγ2/MAPK signaling pathway. Using cecal ligation and puncture (CLP) mouse model to simulate human sepsis, pinocembrin reduced inflammatory cytokine release and septic thrombosis, thereby improving the survival rate of septic mice. Lipopolysaccharide (LPS)-induced model further substantiated these results. Overall, the inhibition of platelet activity by pinocembrin demonstrates significant therapeutic potential for managing life-threatening septic thrombosis.

Autophagy receptor-inspired chimeras: a novel approach to facilitate the removal of protein aggregates and organelle by autophagy degradation.

Neurodegenerative diseases (NDDs), mainly including Huntington's disease (HD), amyotrophic lateral sclerosis (ALS), and Alzheimer's disease (AD), are sporadic and rare genetic disorders of the central nervous system. A key feature of these conditions is the slow accumulation of misfolded protein deposits in brain neurons, the excessive aggregation of which leads to neurotoxicity and further disorders of the nervous system.

The dopaminergic system and Alzheimer's disease.

Alzheimer's disease is a common neurodegenerative disorder in older adults. Despite its prevalence, its pathogenesis remains unclear. In addition to the most widely accepted causes, which include excessive Aβ aggregation, tau hyperphosphorylation, and deficiency of the neurotransmitter acetylcholine, numerous studies have shown that the dopaminergic system is also closely associated with the occurrence and development of this condition. Dopamine is a crucial catecholaminergic neurotransmitter in the human body. Dopamine-associated treatments, such as drugs that target dopamine receptor D and dopamine analogs, can improve cognitive function and alleviate psychiatric symptoms as well as ameliorate other clinical manifestations. However, therapeutics targeting the dopaminergic system are associated with various adverse reactions, such as addiction and exacerbation of cognitive impairment. This review summarizes the role of the dopaminergic system in the pathology of Alzheimer's disease, focusing on currently available dopamine-based therapies for this disorder and the common side effects associated with dopamine-related drugs. The aim of this review is to provide insights into the potential connections between the dopaminergic system and Alzheimer's disease, thus helping to clarify the mechanisms underlying the condition and exploring more effective therapeutic options.

Unravel the Distinctive Roles of Liquid and Solid Additives in Blade‐Coated Active Layer for Organic Solar Cell Modules

AbstractAlthough encouraging progress in spin‐coated small‐area organic solar cells (OSCs), reducing efficiency loss caused by differences in film uniformity and morphology when up‐scaled to large‐area modules through meniscus‐guided coating is an important but unsolved issue. In this work, in‐depth research is conducted on the influence of both liquid and solid additives on the film uniformity and morphology of active layer in blade‐coated PM6:L8‐BO binary system. The study reveals that high boiling point liquid additives like 1,8‐diiodooctane (DIO) used in blade‐coating not only delay the volatilization of the solvent but also trigger the Marangoni flow in the same direction as capillary flow, causing excessive aggregation of acceptors, therefore destroying device performance. On the contrary, the solid additive 2‐Iododiphenyl ether (IDPE), which is first reported in this work, can preserve the mechanism for improving device performance while effectively suppressing the excessive aggregation of acceptors during the film‐forming process in blade‐coating from halogen‐free solvent of toluene, resulting in highly homogeneous large‐area active layer films. Consequently, organic solar modules with an impressive efficiency of 15.34% with a total module area of 18.90 cm2 via blade‐coating based on PM6:L8‐BO are achieved. This study not only provides a deep understanding on the effect of liquid and solid additives during blade‐coating from the perspective of fluid mechanisms but also gives a pathway for the development of green solvent printed high‐efficiency OSCs.

Colloidal Stabilizer‐Mediated Crystal Growth Regulation and Defect Healing for High‐Quality Perovskite Solar Cells

AbstractHigh‐quality perovskite (PVK) films is essential for the fabrication of efficient and stable perovskite solar cells (PSCs). However, unstable colloidal particles in PVK suspensions often hinder the formation of crystalline films with low defect densities. Herein, ethylenediaminetetraacetic acid (EDTA) as a colloidal stabilizer into lead iodide (PbI2) is introduced colloidal solutions. EDTA forms chelated complexes with Pb2+, enhancing the electrostatic repulsion and steric hindrance between colloidal particles. This stabilizes the particles and inhibits disordered motion (Brownian motion) and excessive aggregation. As a result, PbI2 films with a uniform hole distribution are formed, providing ample pathways for subsequent PVK film growth and sufficient space. During the film formation process, the replacement of molecules by formamidinium iodide (FAI) and EDTA slows down crystallization, ultimately leading to PVK films with large grain sizes and low defect density. By using this approach, champion power conversion efficiencies (PCEs) of 24.05% for FA0.97Cs0.03PbI3 PSC, 11.08% for CsPbBr3 PSC, and 25.19% for FA0.945MA0.025Cs0.03Pb(I0.975Br0.025)3 PSC are achieved. Moreover, the EDTA‐based FA0.97Cs0.03PbI3 device retains over 90% of its initial PCE after 1000 h at the maximum power point (MPP) under continuous illumination.

Dipole Moment Modulation of Terminal Groups Enables Asymmetric Acceptors Featuring Medium Bandgap for Efficient and Stable Ternary Organic Solar Cells.

This study puts forth a novelterminal groupdesign todevelopmedium-bandgap Y-series acceptors beyond conventional side-chain engineering.We focused onthe strategical integration of an electron-donating methoxy group and an electron-withdrawing halogen atomatbenzene-fusedterminal groups. This combination preciselymodulatedthedipole moment and electron density of terminal groups, effectively attenuating intramolecular charge transfereffect, and widening the bandgap ofacceptors. The incorporation of theseterminalgroups yielded two asymmetric acceptors, named BTP-2FClO and BTP-2FBrO, both of which exhibited open-circuit voltage (VOC) as high as 0.96 V in binary devices, representing thehighestVOCs among the asymmetric Y-seriessmall molecule acceptors. More importantly, both BTP-2FClO and BTP-2FBrO exhibitmodestaggregation behaviorsandmolecular crystallinity,making themsuitable as a third component to mitigate excess aggregation of the PM6: BTP-eC9 blend and optimize thedevices'morphology.As a result,the optimized BTP-2FClO-based ternary organic solar cells (OSCs) achieved a remarkable power conversionefficiency (PCE)of 19.34%, positioning it among the highest-performing OSCs.Ourstudyhighlights themolecular designimportance on manipulating dipole moments and electron densityindevelopingmedium-bandgap acceptors,andoffersa highly efficient third component forhigh-performance ternary OSCs.

Self-assembling chitosan based injectable and expandable sponge with antimicrobial property for hemostasis and wound healing

Chitosan and chitosan derivative are widely used in hemostasis, antibiosis and wound repair for its good biocompatibility and unique effect. However, the preparation of chitosan based hemostatic materials or wound dressings generally involves chemical crosslinking agent introduction, acid residue or complicated preparation process, which limits its clinical application. In this study, an injectable and expandable chitosan sponge was constructed by chitosan (CS) and quaternized chitosan (QCS) self-assembly without acid retention and chemical crosslinker introduction. In the neutral condition, the hydrogen bond of CS molecules can act as the driving force to form cross-linking network, and the QCS was introduced to regulate the hydrogen bond of CS to avoid the excessive aggregation. The porous QCS/CS sponge was obtained by freeze-drying of the self-assembly QCS/CS hydrogel. The sponge exhibited high expansibility, injectability and water/blood triggered shape memory property. Due to the introduction of QCS, the sponge showed good antibacterial properties, which can protect the wound from bacterial invasion. The convenient and green preparation method of injectable and expandable QCS/CS sponge is a potential method for the treatment of hemostasis and wound healing.

Effects of the main media of wind and water on the biodiversity pattern of grassland and its driving mechanism in Poyang Lake

AbstractAs important media for species diffusion, water and wind are two important factors for grassland biodiversity conservation in lake areas. Exploring their driving mechanism on grassland biodiversity is crucial for maintaining the lake ecosystem's equilibrium. Our study utilizes the data of wind velocity and water level, which are significant performance factors for wind and water respectively in Poyang Lake from 2000 to 2020 to reveal their interannual time‐series fluctuation characteristics and their influence mechanism on the grassland biodiversity pattern. Landscape pattern indices and biodiversity indicators, such as the number of patches (NP), patch density (PD), landscape spreading index (CI), landscape fragmentation index (LSD), landscape aggregation index (AI), Simpson diversity index (MSIDI) and Simpson evenness index (MSIEI) were analysed, trend analysis, redundancy analysis and structural equation modelling were applied in this study. The main results were: (1) From 2000 to 2020, Poyang Lake's wind velocity decreased gradually, and the water level first decreased and then rose. NP in Poyang Lake fluctuated substantially, LSD fluctuated frequently and obvious temporal heterogeneity existed. (2) CI and AI increased from low to high value, facilitating species dispersal and migration. The dominant species with high aggregation gradually established stronger connectivity. Moderate spreading degree and aggregation degree maintained high biodiversity and evenness, whereas excessive spreading degree and aggregation degree led to homogenization of species, decrease in biodiversity, reduction in species evenness, and increase in dominance. (3) As the landscape transformed from having no obvious dominant species to being dominated by several dominant species, MSIEI and landscape dominance changed from high to low and low to high respectively. Moreover, the biodiversity shifted from high to low, and species distribution in the landscape shifted from balanced to unbalanced. (4) The effect of water level on PD, AI, LSD, MSIDI and MSIET was significantly higher than that of wind velocity. LSD was mainly regulated by the minimum wind velocity affecting the maximum and average water levels. MSIDI and MSIET were primarily governed by the minimum wind velocity affecting the minimum water level. The minimum water level decreased as the minimum wind velocity increased, and MSIDI and MSIET weakened as the minimum water level decreased.

Carboxymethylcellulose and rare earth metal cation self-assembly: Tunable encapsulation of carbon dots in a multifunctional transparent film

Due to their unique properties, carbon dots have attracted significant interest across diverse fields. However, obstacles such as uneven size distribution in the course of synthesis and excessive aggregation lead to fluorescence quenching during solidification process. Moreover, conventional doping procedures frequently yield carbon dot films with constrained functionality, inferior durability, and harsh environments, thereby restricting their practical applications. To address these issues, this study fabricates N-doped carbon dots via a straightforward hydrothermal approach and incorporates them into CMC films by metathesis with CeCl3·7H2O, resulting in a unique carbon dot-encapsulated film. This film overcomes the problem of fluorescence quenching caused by excessive aggregation of carbon dots and allows for size control by adjusting the concentration of Ce(III). The resulting film achieves extreme transparency and superior performance compared to existing UV-blocking films. In addition, the film exhibits exceptional resistance to acids and bases, bleaching, excellent mechanical properties, and good thermal and water stability. Based on these properties, the film achieves size-controlled in-situ photoluminescence, full UV shielding, Cu2+ ion detection, anti-counterfeiting, and information encryption. The water-processable and water-adhesive characteristics of CMC enable its use in real-life situations, opening the door to wider use of solid-state carbon dots for multifunctional and intelligent applications.

Fluorinated Naphthalene Diimides as Buried Electron Transport Materials Achieve Over 23% Efficient Perovskite Solar Cells.

Naphthalene diimides (NDI) are widely serving as the skeleton to construct electron transport materials (ETMs) for optoelectronic devices. However, most of the reported NDI-based ETMs suffer from poor interfaces with the perovskite which deteriorates the carrier extraction and device stability. Here, a representative design concept for editing the peripheral groups of NDI molecules to achieve multifunctional properties is introduced. The resulting molecule 2,7-bis(2,2,3,3,4,4,4-heptafluorobutyl)benzo[lmn][3,8]phenanthroline-1,3,6,8(2H,7H)-tetraone (NDI-C4F) incorporated with hydrophobic fluorine units contributes to the prevention of excessive molecular aggregation, the improvement of surface wettability and the formation of strong chemical coordination with perovskite precursors. All these features favor retarding the perovskite crystallization and achieving superior buried interfaces, which subsequently promote charge collection and improve the structural compatibility between perovskite and ETMs. The corresponding PSCs based on low-temperature processed NDI-C4F yield a record efficiency of 23.21%, which is the highest reported value for organic ETMs in n-i-p PSCs. More encouragingly, the unencapsulated devices with NDI-C4F demonstrate extraordinary stability by retaining over 90% of their initial PCEs after 2600 h in air. This work provides an alternative molecular strategy to engineer the buried interfaces and can trigger further development of organic ETMs toward reliable PSCs.

Leveraging Compatible Iridium(III) Complexes to Boost Performance of Green Solvent‐Processed Non‐Fullerene Organic Solar Cells

AbstractIn organic solar cells (OSCs), the short exciton lifetime poses a significant limitation to exciton diffusion and dissociation. Extending exciton lifetime and suppressing recombination are crucial strategies for improving the OSC performance. Herein, an effective approach is proposed by introducing the phosphorescent emitter, tris(2‐(4‐(tert‐butyl)phenyl)‐5‐fluoropyridine)Iridium(III), with long‐lived triplet exciton lifetime in OSCs. This research reveals that the steric structure of fac‐Ir(tBufppy)3 exhibits excellent compatibility with both the donor PM6 and acceptor BTP‐eC9, maintaining efficiencies of over 90% even with a 30% third component loading. Moreover, a 10% addition of fac‐Ir(tBufppy)3 mitigates excessive aggregation in the acceptor BTP‐eC9, optimizing the active layer morphology and improving the fill factor. Transient absorption spectroscopy and transient photoluminescence measurements demonstrate that the introduction of fac‐Ir(tBufppy)3 significantly extends exciton lifetimes and suppresses recombination, which increases the short‐circuit current (JSC). Ultimately, employing the non‐halogenated solvent o‐xylene for processing, an impressive power conversion efficiency (PCE) of 18.54% is achieved in devices based on PM6:10%fac‐Ir(tBufppy)3:BTP‐eC9, surpassing the efficiency of binary PM6:BTP‐eC9 devices (17.41%). This work provides a promising approach to further improve the PCEs in binary OSCs by introducing a phosphorescent iridium(III) complex as the third component.

Amplifying High‐Performance Organic Solar Cells Through Differencing Interactions of Solid Additive with Donor/Acceptor Materials Processed from Non‐Halogenated Solvent

AbstractDeveloping non‐halogenated solvent‐processed organic solar cells (OSCs) demands precise control over the bulk‐heterojunction (BHJ) morphology of the photoactive layer. However, the limited solubility of halogen‐free solvents to photoactive materials hinders microstructure morphology fine‐tuning for boosting photovoltaic performance. This study not only examines the debated intermolecular interactions between the DBrDIB solid additive and photoactive materials but also analyzes the substantial influence of volatile solid additive on the BHJ morphological properties. The DBrDIB effectively restricts the excessive aggregation of Y6‐BO and regulates the phase separation, which is attributed to strong intermolecular interactions with Y6‐BO and rapid quenching during morphology formation. It then achieves a well‐mixed D/A phase with favorable domain size, resulting in a balanced aggregation and dispersion of D/A, ultimately leading to markedly enhanced charge transfer and transport as well as suppressed charge recombination. The transformative use of the o‐xylene/DBrDIB solvent system propels PM6:Y6‐BO and PM6:Y6‐HU OSCs to impressive efficiencies of 17.9% and 19.1%, respectively, outperforming those of the control devices. These findings provide crucial insights into theoretical and experimental areas, offering actionable guidelines for designing high‐performance OSCs processed from halogen‐free solvent.

A triple-benefit strategy of microstructure, electronic property and active site modulation on ZnIn2S4 photocatalyst by Sn atom doping

To overcome the high cost and complex preparation of cocatalysts in photocatalytic H₂ production, this study pioneers a triple-benefit strategy in visible-light-absorbing semiconductors through microstructure optimization, electronic property modulation, and active site modification in two-dimensional (2D) hexagonal ZnIn₂S₄ (ZIS) via Sn atom doping. Facilely synthesized through a one-step hydrothermal method without surfactants, 4–6 nm thick Sn-doped ZIS nanosheets exhibit reduced charge recombination by preventing excessive self-assembly and aggregation. Density Functional Theory (DFT) and X-ray Absorption Fine Structure (XAFS) confirm Sn’s substitution for Zn on (001) surface, shifting the Fermi level into the conduction band to facilitate electron migration and charge separation. This adjustment also modulates the electronic properties of adjacent S atoms, triggering the inert basal plane for an enhanced H₂ evolution reaction kinetics. Consequently, Sn-ZIS achieves a H₂ evolution rate of 62.18 μmol h−1 under visible light, significantly outperforming pure ZIS and Pt@ZIS by 6.7 and 3.5 times, respectively.

Er2O3 doped ZnO–Cr2O3-based varistors with high voltage gradient

ZnO varistors are widely used in modern intelligent electrical equipment, and the preparation of miniaturized varistors with high voltage gradient has become a top priority. This work investigated the preparation of high voltage gradient ZnO–Cr2O3-based varistors doped with Er2O3 and analyzed the relationship between their microstructure and electrical properties. As the doping amount of Er2O3 increases from 0.00 to 0.75 mol%, Er2O3 phase obviously dissolving element Co distributed at the trigeminal grain boundaries increases, leading to the grain size d decreases from 3.16 to 1.70 μm, the nonlinear coefficient α increases from 6.22 to 50.48, the voltage gradient E1mA increases from 428.37 to 1616.76 V/mm, and the leakage current density JL decreases from 375.75 to 0.79 μA/cm2, achieving optimal comprehensive electrical performance of the sample with Er2O3 doping of 0.75 mol%, for which, the residual voltage ratios K reaches the minimum value of 1.14 under the impulse current density Jp of 63.7 A/cm2. When the doping amount of Er2O3 further increases to 1.00 mol%, the excessive Er2O3 phase aggregates at the trigeminal grain boundaries and distributes unevenly, leading to the growth of ZnO grains and performance deterioration of the samples. The ZnO–Cr2O3-based varistors have the advantages of much easier doping, and there is no dopant volatilization during the sintering process. This research provides an important reference for the development of high-performance, miniaturized ZnO–Cr2O3-based varistors.