Cell Layer Research Articles

Histological Characteristics of Follicles, Reproductive Hormones and Transcriptomic Analysis of White King Pigeon Illuminated with Red Light.

Red light (RL) has been observed to enhance egg production in pigeons, yet the underlying histological characteristics and molecular mechanisms remain less understood. This study included fifty-four pigeons to assess follicular histology, reproductive hormones, and ovarian transcriptomics on the third day of the laying interval under RL and white light (WL). The results showed that the granulosa cell layer was significantly thicker under RL (p < 0.05), whereas the theca cell and connective tissue layers showed no significant differences (p > 0.05). Higher plasma estradiol (E2) levels were recorded in the RL group (p < 0.05), as well as follicle stimulating hormone (FSH), although progesterone (P4) levels were higher under WL (p < 0.05). Moreover, P4 concentrations in follicle yolk significantly decreased under RL (p < 0.01), with higher FSH and E2 levels in F1 yolk and similar increases in SF1 yolk (p < 0.01). Transcriptomic analysis revealed 4991 differentially expressed genes in the pigeon ovary. The protein-protein interaction network highlighted genes like HSD11B1, VEGFD, WNT6, SMAD6, and LGR5 as potential contributors to hierarchical follicle selection under RL. This research provides new insights into the molecular basis by which RL may promote hierarchical follicle selection and improve egg production in pigeons.

Effects of K, Rb, and Br doping on Cs3Bi2I9 perovskites: A design of experiments approach

This work presents the effect of doping with different species on the structural sites of lead-free halide perovskites, aiming to evaluate the potential of the produced materials as photoabsorbing layers in 3rd generation solar cells. Lead-free perovskite films of Cs3Sb2I9, CsCu2I3, Cs3Bi2I9, and CsPbI3 were synthesized via the spin-coating method and characterized using X-ray diffraction, scanning electron microscopy with chemical microanalysis (SEM-EDS), and Uv-Vis spectroscopy. Computational models based on Density Functional Theory (DFT) were used to simulate the structures and properties of some of the perovskites synthesized in this study, in order to validate the experimentally obtained data. The Cs3Bi2I6Br3 perovskite was subjected to modification through A-site doping with K and Rb and X-site doping with Br, with a comprehensive study on the effects of processing variables, anti-solvent quantity, and crystallization temperature using a 23 experimental design. The outcomes highlighted the critical role of the anti-solvent quantity in structure formation and electronic properties. Toluene, as an anti-solvent, produced unique morphologies not commonly reported. Computational studies were performed using Density Functional Theory (DFT) to complement the experimental findings. The optimization process revealed that Cs3Bi2I9 structures mainly constituted [CsI12] and [BrI6] clusters, with Cs–I and Bi–I average bond lengths consistent with experimental results. X-site Br doping induced slight distortion, while A-site Rb/K doping showed minimal lattice parameter changes. Notably, K-induced morphological alterations suggested potential electronic transformations. From an electronic structure perspective, Cs3Bi2I9 had a band gap of 2.07 eV, slightly increased to 2.10 eV with Br doping. Rb maintained Br-doped structure, while K significantly reduced the band gap to 1.96 eV. These computational results align well with our experimental data, showcasing the accuracy of our calculations in predicting material properties. The results confirmed that the perovskites selected through experimental design and validated by computational simulation are promising semiconductor materials for photovoltaic applications, as well as being a lead-free photoabsorbing material option.

Composites electron transport layer of PVA-regulated SnO2 for high-efficiency stable perovskite solar cells

As a new and efficient solar cell, perovskite solar cell has attracted wide attention due to its excellent performance. The electron transport layer in perovskite solar cells has a significant impact on device performance. SnO2 films that can be prepared by solution method have become the first choice for electron transport layer due to their simple process and excellent performance. However, the defects in SnO2 thin films and non-radiative recombination sites at the SnO2/Perovskite interface will lead to potential losses in the performance of photovoltaic devices. Therefore, in order to improve the interface loss and interface characteristics and prepare more efficient perovskite solar cells. In this work, a functional polymer, polyvinyl alcohol (PVA), is introduced to regulate the arrangement of SnO2 nanocrystals. The SnO2-PVA composite electron transport layer not only improves carrier transport, but also further affects the growth of perovskite films. PVA inhibits the agglomeration of tin dioxide particles by adding it to the aqueous solution of tin dioxide. Meanwhile, the oxygen vacancy defects in the SnO2 layer have also improved. Correspondingly, SnO2-PVA-based PSCs can be obtained a maximum efficiency of 23.73 %. Attributed to the strengthened interface binding and the improved perovskite crystallization process, the devices obtain good long-term stability, retaining 90 % of their initial performance after 1000 h operation at their maximum power point under 1 sun illumination.

Characterising Skin Electrical Impedance Using Tape Stripping Methods: A Bioelectrical Study of a Porcine Model.

Background Recent advancements in ultra-low power electronics and wireless devices have facilitated the widespread adoption of wearable technology for fitness and health monitoring, paving the way for personalized medicine. Microneedle-based devices, comprising small epidermal patches that penetrate the skin's stratum corneum to potentially access biomarkers in the extracellular fluid of the viable epidermis, represent a promising innovation in this field. Objectives This project aimed to develop and validate a novel method to evaluate microneedle engagement in the skin in real-time. To our knowledge, there are no studies published to date that have characterized the electrical impedance of stratum corneum and epidermis using the tape stripping method to selectively remove cell layers. Additionally, no studies have been published comparing the electrical impedance of fresh to frozen-thawed porcine skin. The objective of this study was to develop and validate a novel method to evaluate microneedle engagement in skin, in real-time, that does not require processing of the tissue. Methods A tape stripping technique was employed to selectively remove the stratum corneum from fresh and frozen-thawed porcine skin samples which were then electrically characterized using an excitation frequency of 5 kHz with a peak Voltage of 1 V. Results This study demonstrated a mean impedance reduction of 97.08 ± 1.3 % for fresh porcine skin, and 98.04 ± 0.3 % for frozen-thawed porcine skin when transitioning from the surface stratum corneum to the viable epidermis. The correlation between the reduction of impedance and the number of tape strips across all 18 test sites was significant (r = 0.98, p < 0.00001). However, comparing the skin impedance of the fresh and frozen-thawed specimens showed poor equivalence, with the frozen-thawed sites approximately 5.5 times the impedance of the fresh sites before any tape stripping, and 4.19 times greater after 30 tape strips. Conclusions These findings suggest that monitoring for an interelectrode impedance decrease of greater than 95% between two projections of a microneedle device could provide a rapid and effective evaluation of skin engagement, crucial for advancing the development and clinical application of microneedle-based technologies in personalized medicine. The study also underscores the impact of the freeze-thaw process on the mechanical and electrical properties of skin, which is crucial for standardizing testing protocols.

MicroRNA-based engineered mesenchymal stem cell extracellular vesicles to treat visual deficits after blast-induced trauma

Our previous studies have shown the benefit of intravitreal injection of a mesenchymal stem cell (MSC)- derived secretome to treat visual deficits in a mild traumatic brain injury (mTBI) mouse model. In this study, we have addressed whether MSC-derived extracellular vesicles (EV) overexpressing miR424, which particularly targets neuroinflammation, show similar benefits in the mTBI model. Adult C57BL/6 mice were subjected to a 50-psi air pulse on the left side, overlying the forebrain, resulting in mTBI. Sham-blast mice were controls. Within an hour of blast injury, 3 μl (∼7.5 × 108 particles) of miR424-EVs, native-EVs, or saline was delivered intravitreally. One month later, retinal morphology was observed through optical coherence tomography (OCT); visual function was assessed using optokinetic nystagmus (OKN) and electroretinogram (ERG), followed by immunohistological analysis. A separate study in adult mice tested the dose-response of EVs for safety. Blast injury mice with saline showed decreased visual acuity compared with the sham group (0.30 ± 0.03 vs. 0.39 ± 0.01 c/d, p < 0.02), improved with miR424-EVs (0.39 ± 0.02 c/d, p < 0.01) but not native-EVs (0.33 ± 0.04 c/d, p > 0.05). Contrast sensitivity thresholds of blast mice receiving saline increased compared with the sham group (85.3 ± 5.9 vs. 19.9 ± 4.8, %, p < 0.001), rescued by miR424-EVs (23.6 ± 7.3 %, p < 0.001) and native-EVs (45.6 ± 10.7 %, p < 0.01). Blast injury decreased “b” wave amplitude compared to sham mice (94.6 ± 24.0 vs. 279.2 ± 25.3 μV, p < 0.001), improved with miR424-EVs (173.0 ± 27.2 μV, p < 0.03) and native-EVs (230.2 ± 37.2 μV, p < 0.01) with a similar decrease in a-wave amplitude in blast mice improved with both miR424-EVs and native-EVs. Immunohistology showed increased GFAP and IBA1 in blast mice with saline compared with sham (GFAP: 11.9 ± 1.49 vs. 9.1 ± 0.8, mean intensity/100,000 μm2 area, p < 0.03; IBA1: 36.08 ± 4.3 vs. 24.0 ± 1.54, mean intensity/100,000 μm2 area, p < 0.01), with no changes with native-EVs (GFAP: 12.6 ± 0.79, p > 0.05; IBA1: 32.8 ± 2.9, p > 0.05), and miR424-EV (GFAP: 13.14 ± 0.76, p > 0.05; IBA1: 31.4 ± 2.7, p > 0.05). Both native-EVs and miR424-EVs exhibited vitreous aggregation, as evidenced by particulates in the vitreous by OCT, and increased vascular structures, as evidenced by αSMA and CD31 immunostainings. The number of capillary lumens in the ganglion cell layer increased with increased particles in the eye, with native EVs showing the worst effects. In conclusion, our study highlights the promise of EV-based therapies for treating visual dysfunction caused by mTBI, with miR424-EVs showing particularly strong neuroprotective benefits. Both miR424-EVs and native-EVs provided similar protection, but issues with EV aggregation and astrogliosis or microglial/macrophage activation at the current dosage call for improved delivery methods and dosage adjustments. Future research should investigate the mechanisms behind EVs' effects and optimize miR424 delivery strategies to enhance therapeutic outcomes and reduce complications.

Small Polaron Dynamics in Transition Metal Oxide Photoelectrodes

The transition metal oxides are widely used in many optoelectronic applications, such as working as charge-transporting layers in solar cells and photoelectrodes in light-driven water-splitting. Considering the ionic bonding nature, the lattice of these oxides can be polarized by the charge carriers due to the strong electron-phonon coupling, giving rise to lattice distortion that fosters a local potential well. This lattice distortion together with the trapped carrier is regarded as a quasi-particle, i.e., a polaron. Here, the photocarrier dynamics in transition metal oxides were investigated using the transient absorption and time-resolved terahertz spectroscopies. We identified the spectral features of small polarons, self-trapped excitons, and free carriers and extracted their dynamics independently. We proposed a molecular model that could successfully explain the non-barrier self-trapping and quantitatively describe the temperature-dependent recombination of self-trapped excitons and the dopant effect on the photocarrier dynamics. Our model also suggested that the recombination of self-trapped excitons at room temperature was dominated by nuclear quantum tunneling. This model also predicted the micro-heterogeneity of the self-trapped species, and thus be able to quantitatively describe the Auger annihilation dynamics of self-trapped excitons.

Exploring the Photoluminescence Characteristics of Nitrogen-Doped Carbon Dots

Carbon dots, or C-Dots, are graphitic particles below 10 nm that exhibit room temperature photoluminescence (PL). The specific PL mechanism of C-Dots varies with synthesis paths and remains unresolved. This study utilizes direct current microplasmas for reliable and reproducible synthesis, exploring precursor outcomes and the discharge current's impact on surface chemistry and optical properties. The nitrogen-doped C-Dots (N-CQDs) synthesized display crystalline structures with a graphitic core, nitrogen doping, and a functionalized surface. Luminescence, originating from both core and surface states, can be finely controlled by adjusting synthesis conditions. N-CQDs, with a high photoluminescence quantum yield, hold promise for next-gen solar cell applications. The N-CQDs exhibit intriguing quantum-confined optical properties dependent on the level of nitrogen incorporation. Notably, the band energy structure of the N-CQDs is clarified, and they are integrated into a photovoltaic device as the photoactive layer, achieving an extraordinary open-circuit voltage of 1.8 V corroborating well with energy gat of CQDs and PL properties [1, 2]. We specifically highlight the use of nitrogen-doped C-Dots as an active absorbing layer in solar cells and discuss how doping can engineer their electrical, optical, and chemical properties. Nitrogen doping mainly occurs in the graphitic core as a substituted type of doping (63–67 atomic%), with enough to create emissive states without impacting the core structure. The optical and chemical properties remain stable even with re-dispersion, suggesting easy applicability for cellular imaging or optoelectronics [3]. Highly stable nitrogen-doped graphite quantum dots, prepared by atmospheric pressure microplasma, without post-synthesis treatments, yields stable, water-dispersible, and non-toxic quantum dots with a high PL quantum yield of approximately 70%.

New Electrocatalyst with the Content of Ir

Introduction Proton exchange membrane (PEM) water electrolysis (WE) is a promising technology for hydrogen production. However, the local environment of the anode in PEMWE is highly acidic and high potential due to the oxygen evolution reaction (OER; 2H2O → O2 + 4H+ + 4e-), and the available anode materials are limited to precious metal elements such as Pt, Ru and Ir. In the current technology, Ir-based materials are the mainstream anode catalysts, and Ir loading of 1-2 mg/cm2 is necessary to achieve both activity and durability. On the other hand, the annual production of Ir is said to be only 5-7 tons. The demand for hydrogen is expected to increase to the GW scale in the future. For example, if water electrolysis is operated at 2 A/cm2 and 2 V with Ir loading of 2 mg/cm2 (0.5 mgIr/W), it is difficult to meet the demand with the existing Ir resources. Tosoh have been engaged in the electrolytic manganese dioxide (EMD) business. EMD is synthesized thorough anodic oxidation of Mn2+ ion (Mn2+ + 2H2O → MnO2 + 4H+ + 2e-) under acidic conditions, therefore it is potentially suitable for the anode environment of PEMWE. In this study, a very small amount of Ir (<0.1 mg/cm2) was successfully composited with EMD. The resulting composite consisting of Ir and EMD showed more active than commercial Ir oxide with the same Ir content, and operated stably for at least 1000 h. Experiment EMD thin film was electrodeposited anodically on Pt-coated Ti fibers (Pt/Ti) thorough electrolyzing a mixed solution of MnSO4 and H2SO4. The obtained EMD-coated Pt/Ti were immersed in an Ir-containing solution, and then annealed to obtain Ir-containing EMD (hereinafter referred to as "Ir-EMD"). The Pt-coated Ti fibers are used as a porous transport layer (PTL) in PEMWE cells, and our developed material serves as both an OER catalyst and a PTL. OER property was evaluated using a PEMWE cell at 80°C in a two-electrode system. Pt-supported carbon was used as the cathode catalyst and Nafion®-115 as the PEM. See Fig. 1 for PEMWE cell construction flow. Result and discussion The Ir content in Ir-EMD was determined to be 0.1 mg/cm2 by ICP-AES. This Ir content is 10-20 times lower than that used in current PEMWE electrolyzers. The OER activity of Ir-EMD was evaluated by linear sweep voltammetry (LSV) (Fig. 2). For comparison, EMD (with no Ir) and Ir oxide (commercial product) with an Ir content of 0.1 mg/cm2 were evaluated in the same way. The slow OER property of EMD was improved dramatically by introducing Ir into EMD. Also, at the same amount of Ir, Ir-EMD exhibited higher OER activity than that of Ir oxide. The inset in Fig. 2 shows Tafel plots corresponding to LSVs, and the slope of the linear region (Tafel slope) can be used to predict which elementary reaction is the rate-limiting step in the OER. The Tafel slope of Ir-EMD is 58 mV/dec., which is close to the Tafel slope of Ir oxide, 50 mV/dec. This suggests that OER on Ir-EMD proceeds by the same mechanism as Ir oxide. The durability of Ir-EMD and Ir oxide was tested at a current density of 2 A/cm2 (Fig. 3). Ir oxide was deactivated within only 8 days, and it is confirmed that Ir have disappeared after electrolysis. On the other hand, Ir-EMD has operated stably for more than 42 days (≈1000 h), with a degradation rate of only 13 μV/h. In other words, Ir-EMD has practical durability while reducing the amount of Ir by more than 10 times compared to current technology.Acknowledgements : This presentation is based on results obtained from a project, JPNP20003, subsidized by the New Energy and Industrial Technology Development Organization (NEDO). Figure 1

Development of a 4-in-1 Device to Measure Component Properties of Gas Diffusion Layer/Porous Transport Layer for Both Proton Exchange Membrane Fuel Cell and Water Electrolyzer

This work aims at developing a 4-in-1 device to simultaneously measure parameters under compression (UC), including thickness (TUC), resistivity (RUC, through-plane), and in-plane permeability (IPP-UC), and to separately measure through-plane permeability (TPP). The simultaneous measurement of TUC/RUC/IPP-UC is accomplished through an annulus sample by measuring the flow rate–pressure relationship in a radial flow [1]. By adding a two-piece adaptor, TPP can also be measured using a disk sample. Typical TUC/RUC/IPP-UC/TPP curves of a gas diffusion layer (GDL) are shown in Figure 1. Upon the design requirements, the TUC/RUC/IPP-UC/TPP tester is calibrated and validated.The 4-in-1 device was originally designed for the characterization of the GDL, a key component of the membrane electrode assembly (MEA) for a proton exchange membrane (PEM) fuel cell. The GDL properties are greatly associated with the cell performance, especially under compression. To ensure the quality of GDLs, it is of great importance to characterize GDL properties with respect to the component standardization and specification. The application of the 4-in-1 device was later extended for the characterization of the porous transport layer (PTL), a crucial component for the anode of PEM water electrolyzer in responding to the increased research and efforts made in the development of, mostly, Ti-based PTLs for PEM water electrolysis [2]-[4] , as commercially available PTLs are basically materials borrowed from other applications, e.g., filtration.The developed TUC/RUC/IPP-UC/TPP device has been proven to be a useful tool for the quality control (QC) of GDLs and PTLs, facilitating the component development, complementing the component supply chain, contributing to cell reliability, and thus reduction of cost, for both the PEM fuel cell and PEM water electrolysis technologies. Acknowledgements This work is financially supported by the Office of Energy Research and Development (OERD) and the Advanced Clean Energy (ACE) Program of the National Research Council Canada (project #NRC-23-140).

Electrodeposited mesoporous TiO2 thin films and their application as the scalable electron transport layer for perovskite solar modules

In this study, we present the utilization of electrodeposited TiO2 mesoporous film (ED-MS-TiO2) as the electron transport layer (ETL) for perovskite solar cells, especially marking the first report of its application in perovskite solar modules. In the first part of this paper, we refine the electrodeposition process to enhance the porosity of the ED-MS-TiO2 thin film by elevating the ED temperature from room temperature to a mild 60 °C. Notably, the ED-MS-TiO2 ETL fabricated at 60 °C demonstrates comparable charge extraction capability and conversion efficiency to the benchmark ETL produced via the widely adopted spin-coating technique, achieving a remarkable 20.5 %. Furthermore, we demonstrate the immense superiority of the ED process in achieving uniformity in the preparation of large-area ETLs. Our current findings reveal that ED-MS-TiO2 exhibits exceptional uniformity control, with a thickness distribution of 122.69 ± 8.39 nm on a 100 cm² substrate, while its spin-coated counterpart exhibits poor thickness control, measuring 135.72 ± 50.72 nm. Moreover, perovskite solar modules (5 cm × 5 cm) employing the optimized ED-MS-TiO2 ETL attain an impressive efficiency of 15.63 %, surpassing counterparts utilizing spin-coated TiO2 ETLs, which achieve only 9.70 %.

Solvent-Activated Transformation of Polymer Configurations for Advancing the Interfacial Reliability of Perovskite Photovoltaics.

Organic materials have been widely used as the charge transport layers in perovskite solar cells due to their structural versatility and solution processability. However, their low surface energy usually causes unsatisfactory thin-film wettability in contact with the perovskite solution, which limits the interfacial performance of the photovoltaic devices. Although solvent post-treatment could occasionally regulate the wetting behavior of organic films, the mechanism of the solid-liquid interaction is still unclear. Here, we present evidence of a possible correlation between the solvent and the wettability of a conventional polymer, poly[bis(4-phenyl) (2,4,6-trimethylphenyl) amine] (PTAA), and reveal the critical roles of Hansen solubility parameters (HSPs) of solvents in wetting mechanisms. Our results suggest that the conventional solvent N,N-dimethylformamide (DMF) improves the wettability of PTAA by the morphological disruption mechanism but negatively impacts interfacial charge collection and stability. In contrast, 2-methoxyethanol (2-Me) with an appropriate HSP value induces the transformation of the PTAA configuration in an orderly manner, which simultaneously improves the wetting property and maintains the film topography. After careful optimization of the surface conformation of the PTAA film, both perovskite crystallization and interfacial compatibility have been enhanced. Benefiting from superior interfacial properties, the perovskite solar cells based on 2-Me deliver a champion efficiency of 24.15% compared to 21.4% for DMF-based ones. More encouragingly, the use of 2-Me minimizes the perovskite buried interfacial defects, enabling the unencapsulated devices to maintain about 95% of their initial efficiencies after light illumination for 1100 h. The present study demonstrates the high effectiveness of solvent-polymer interaction for adjusting interfacial properties and strengthening the robustness of perovskite solar cells.

Pathological evaluation of predictors for delayed endothelial coverage after currently available drug-eluting stent implantation in coronary arteries: Impact of lesions with acute and chronic coronary syndromes

BackgroundThe optimal duration of dual antiplatelet therapy after currently available drug-eluting stent (DES) implantation to prevent stent thrombosis (ST) remains controversial. Delayed healing is frequently identified as a leading cause of ST in the early phase. However, a thorough pathological investigation into strut coverage after currently available DES implantation is lacking—a gap addressed in the current study. MethodsFrom our autopsy registry of 199 stented lesions, 4,713 struts from 66 currently available DES-stented lesions with an implant duration ≤370 days were histologically evaluated. Endothelial coverage was defined as the presence of luminal endothelial cells overlying struts and an underlying smooth muscle cell layer. The stented lesions were classified into acute coronary syndrome (ACS) (n = 40) and chronic coronary syndrome (CCS) (n = 26) groups and were compared. Endothelial coverage predictors were identified through logistic analysis. ResultsAlthough ACS and CCS lesions presented comparable clinical characteristics, including age, sex, and cause of death, the latter exhibited a significantly higher prevalence of chronic kidney disease and hemodialysis than the former (33.3% vs. 65.2%; p = 0.02, 7.7% vs. 30.4%; p = 0.02). The poststent implant median duration was significantly shorter in ACS lesions than in CCS lesions (13 [IQR 5–26 days] vs. 40 [IQR 16–233 days]; p < 0.01). The endothelial coverage percentage was 3.5% at 30 days and 27.7% at 90 days after currently available DES implantation. Multivariable logistic regression analysis implicated implant duration of ≤90 days [odds ratio (OR), 0.009; 95% confidence interval (CI), 0.006–0.012; p < 0.01], superficial calcification (OR, 0.11; 95% CI, 0.07–0.17; p < 0.01), ACS culprit site (OR, 0.29; 95% CI, 0.09–0.94; p = 0.039), and circumferentially durable polymer-coated DES (OR, 0.32; 95% CI, 0.24–0.41; p < 0.01) as delayed endothelial coverage predictors. ConclusionsEndothelial coverage was limited at 90 days after currently available DES implantation, and the ACS culprit site and circumferentially durable polymer-coated DES were identified as independent predictors of delayed endothelial coverage. Our findings suggest the importance of underlying plaque morphology and stent technology for vessel healing after such implantation.

Efficiency improvement of antimony selenide solar cells based on S-doped SnO2 buffer layer

Antimony Selenide (Sb2Se3) exhibits potential as a solar energy material owing to its optimal bandgap, lack of toxicity, and abundance of earth abundant elements. Currently, cadmium sulfide (CdS) serves as the predominant buffer layer for Sb2Se3 solar cells. However, the use of CdS hinders environmentally friendly advancement due to the toxic properties of the element cadmium. Hence, the quest for non-toxic buffer layers poses a significant challenge to the further advancement of Sb2Se3 solar cells. In prior research, tin oxide (SnO2) has been explored as a buffer layer. Nonetheless, the efficiency of SnO2/Sb2Se3 solar cells was hampered by the rough surface of SnO2 films and the poor crystallinity of Sb2Se3 films. In this investigation, we enhanced device efficiency by improving the uniformity of the SnO2 surface and enhancing the crystallinity of Sb2Se3 through spin-coating sulfur (S) onto the SnO2 film. Detailed examinations were conducted on the structure, optical, and electrical properties of the respective SnO2 and Sb2Se3 thin films. Ultimately, an efficiency of 3.38% was achieved using the spin-coated S:SnO2 film, marking an 85% enhancement compared to the baseline device.

A Mouse Model for Conditional Expression of Activated β-Catenin in Epidermal Keratinocytes.

We report the generation and characterization of the K5: CAT bigenic mouse in which the constitutively activated form of β-catenin (ΔN89 β-catenin) is conditionally expressed in cytokeratin-5 (K5) positive epidermal keratinocytes. Following short-term doxycycline intake during the telogen resting phase, the adult K5: CAT bigenic develops enlarged pilosebaceous units that expand deep into the dermis, an expansion usually observed during the anagen growth phase. Prolonged doxycycline treatment results in significant thickening and folding of the K5: CAT epidermis. During this persistent induction period, there is clear evidence of increased keratinocyte proliferation, particularly in the epidermal basal cell layer and the outer root sheath of the hair follicle. This unscheduled increase in cellular proliferation likely explains the decrease in hair density observed in the K5: CAT mouse following persistent doxycycline intake. Numerous hyperplastic endometrioid cysts, which display cornification toward their lumens, are also observed during this treatment period. Remarkably, de-induction of ΔN89 β-catenin expression through doxycycline withdrawal results in a marked reversal of the skin phenotype, suggesting that these morphological changes are dependent on continued signaling by β-catenin and/or its downstream molecular mediators. Joining a small group of mouse models for conditional β-catenin signaling, our K5: CAT mouse model will be particularly useful in identifying those molecular mediators of β-catenin that are responsible for initiating and maintaining these phenotypic responses in the K5: CAT skin. Such studies are predicted to shed more light on β-catenin signaling in epidermal epithelial morphogenesis, hair follicle cycling, and hair growth pathologies.

Utilization of Polycyclic Aromatic Solid Additives for Morphology and Thermal Stability Enhancement in Photoactive Layers of Organic Solar Cells.

Volatile solid additives have emerged as a promising strategy for enhancing film morphology and promoting the power conversion efficiency (PCE) of organic solar cells (OSCs). Herein, a series of novel polycyclic aromatic additives with analogous chemical structures, including fluorene (FL), dibenzothiophene (DBT), and dibenzofuran (DBF) derived from crude oils, are presented and incorporated into OSCs. All these additives exhibit strong interactions with the electron-deficient terminal groups of L8-BO within thebulk-heterojunction OSCs. Moreover, they demonstrate significant sublimation during thermal annealing, leading to increase free volumes for the rearrangement and recrystallization of L8-BO. This phenomenon leads to an improved film morphology and an elevated glass-transition temperature of the photoactive layers. Consequently, the PCE of the PM6:L8-BO blend has been boosted from 16.60% to 18.60% with 40 wt% DBF additives, with a champion PCE of 19.11% achieved for ternary PM6:L8-BO:BTP-eC9 OSCs. Furthermore, the prolonged shelf and thermal stability have been observed in OSCs with these additives. This study emphasizes the synergic effect of volatile solid additives on the performance and thermal stability of OSCs, highlighting their potential for advancing the field of photovoltaics.

Aggregation Regulation of Acceptor via Thiophene‐Substituted Alkyl Chains Enables High‐Performance Toluene‐Processed Organic Solar Cells without Additive and Post‐Treatment

AbstractDue to the mismatched aggregation behavior and limited compatibility between the donor and acceptor, it is a challenge for the active layer of organic solar cells (OSCs) to spontaneously realize well‐developed morphology in nonhalogenated solvents. In this contribution, an aggregation regulation strategy for acceptors with strong aggregation is developed via thiophene‐substituted alkyl chain engineering to fabricate high‐performance nonhalogenated solvent‐processed OSCs without an additive or post‐treatment. With the replacement of alkyl chains with steric conjugated thiophene‐substituted alkyl chains, the resulting acceptor (namely BTP‐2T, BTP‐T, and BTP‐T‐BO) shows reduced aggregation to match the polymer donor D18‐Cl using toluene as a processing solvent, enabling ordered molecular arrangement and uniform phase separation morphology. Especially, the combined modification of the asymmetric thiophene‐substituted inner chain and branched outer side chains for BTP‐T‐BO enables the formation of a superior nanoscale bi‐continuous interpenetrating network along with ordered and compact molecular packing in the D18‐Cl:BTP‐T‐BO blend. As a result, an excellent PCE of 18.05% is achieved in the D18‐Cl:BTP‐T‐BO‐based device using toluene as the processing solvent without any extra treatment, which is the highest value for nonhalogenated solvent‐processed OSCs without any extra treatment.

The Macular Pigment Optical Density (MPOD) Decrease in Chinese Primary Angle Closure Glaucoma Using the One-Wavelength Reflectometry Method

Purpose The objective of this study was to observe the macular pigment optical density (MPOD) and the relationship between MPOD and retinal thickness in Chinese primary angle-closure glaucoma (PACG) patients by the one-wavelength reflectometry method. Methods This study was a prospective comparative observational study, including 39 eyes from 39 PACG patients (15 men and 24 women, mean age 61.89 ± 12.30) and 41 eyes from 41 controls (20 men and 21 women, mean age 63.24 ± 14.02). We measured the MPOD 7-degree area by the one-wavelength reflectometry method and analyzed both the max and mean optical density (OD). The central retinal thickness (CRT) and the total thickness of the macular ganglion cell layer (GCL), and inner plexiform layer (IPL)were measured by spectral-domain-optical coherence tomography (SD-OCT). Statistical methods such as Shapiro–Wilk test, Fisher’s exact test, chi-square test, two independent samples test and Spearman’s correlation coefficient were used to observe the differences in the MPOD between normal subjects and PACG patients and the correlation between the MPOD and retinal thickness. Results The max optical density (Max OD) (PACG group: 0.302 ± 0.067d.u, control group: 0.372 ± 0.059d.u., p < .001) and mean optical density (Mean OD) (PACG group: 0.124 ± 0.035d.u., control group: 0.141 ± 0.028d.u., p < 0.05) were significantly reduced in PACG patients compared with control subjects. Significant decreases in GCL + IPL thickness (PACG group: 74.71 ± 39.56 μm, control group:113.61 ± 8.14 μm, p < 0.001) and CRT (PACG group: 254.49 ± 41.47 μm, control group:329.10 ± 18.57 μm, p < 0.001) were also observed in PACG eyes. There was no statistically significant correlation between the MPOD and GCL + IPL thickness (p = .639, p = .828). Conclusions MPOD was significantly lower in Chinese PACG patients than in the control group, potentially due to thinning of the GCL + IPL thickness. This study provides insights for the pathophysiology, assessment of PACG and potential guidance for lifestyle modifications.

Optic Atrophy From Retrograde Transsynaptic Axonal Degeneration Following Pediatric Brain Injury.

The patterns of optic atrophy due to retrograde transsynaptic degeneration (RTSD) have not been well characterized in children. This study aimed to characterize optic atrophy in pediatric patients with focal intracerebral lesions. A retrospective review of children with optic atrophy and focal intracerebral lesions was conducted. Ophthalmic data were recorded, including visual acuity, color vision, formal automated visual fields and optical coherence tomography (OCT) of the peripapillary retinal nerve fiber layer (pRNFL) and ganglion cell layer. Six patients (83.33% male) were included. The mean visual acuity (VA) of all eyes was 0.30 logMAR (20/40 Snellen), with no significant difference in the mean logMAR VA in the ipsilateral eye to the location of the lesion compared with the contralateral eye (0.30 vs 0.30, P = 1.000). Color vision (available in 5 patients) was normal in 2, mildly reduced in one and markedly reduced in 2. Bitemporal optic disc pallor was observed in 5 out of 6 patients. OCT data revealed that pRNFL thickness was most significantly diminished in the temporal (95% CI: -44.71 to -14.18 µm, P = 0.0021), inferotemporal (95% CI: -75.06 to -5.17 µm, P = 0.0294), and superotemporal (95% CI: -76.82 to -18.51 µm, P = 0.0055) sectors. Average pRNFL thickness was significantly reduced compared with normative data in both the ipsilateral (95% CI: -40.76 to -11.69 µm, P = 0.0003) and the contralateral eye (95% CI: -38.46 to -5.83 µm, P = 0.0063). When only nasal and temporal data were analyzed, mean pRNFL thickness was still diminished compared with normative data (95% CI: -33.01 to -9.77 µm, P = 0.0012). Children presenting with optic atrophy, particularly with bitemporal optic atrophy, should have neuroimaging to exclude any underlying serious intracranial pathology.

Stearic acid as a potential interlayer at the FAPI/hole transport layer interface

In this study, we explore the potential of using an ultra-thin film of stearic acid (SA) as an interlayer at the interface between the active material and the hole transport layer (HTL) in perovskite solar cells (PSCs). The FAPbI3 active material thin film was fabricated under ambient conditions using the antisolvent method, followed by the deposition of stearic acid overlayers of varying coverages/thicknesses. By adjusting the coverage/thickness of the SA overlayer, the electronic structure of the perovskite surface can be finely tuned, which may potentially lead to favorable energy level alignment at the perovskite/HTL interface. The interaction between the perovskite thin film and the stearic acid overlayer is expected to involve coordination between defects on the perovskite surface and the carboxyl group of stearic acid. The presence of the nonpolar alkyl chain of stearic acid on the perovskite surface enhances material stability by preventing water and oxygen ingress. Our findings suggest that introduction of SA interlayer at the perovskite/HTL interface may enhance operational stability and efficiency of PSCs by improving the charge transfer across the interface through optimization of energy level alignment and reduction of recombination sites, and protect the absorber from environmental factors like water and oxygen.

Synergistically Regulating CBD‐SnO2/Perovskite Buried Interface for Efficient FAPbI3 Perovskite Solar Cells

AbstractTin oxide (SnO2) based on chemical bath deposition method (CBD‐SnO2) is considered as an ideal electron transporting layer for perovskite solar cells (PSCs), however, the research on precise regulation toward CBD‐SnO2 layer is lacking. Here, the study introduces a multifunctional molecule, potassium 2‐(N‐morpholino)ethanesulfonate (MES‐K), on the surface of CBD‐SnO2 layer to synergistically modify the buried interface between the SnO2 and perovskite. It is found that MES‐K introduction can passivate interfacial defects, favor the perovskite crystal growth, and improve carrier transportation. 25.14% efficiency of small‐size perovskite solar cells has been achieved with 24.45% efficiency of 1 cm2 perovskite devices, with negligible hysteresis. Besides, unencapsulated devices based on CBD‐SnO2 can maintain &gt; 95% of its initial efficiency after 2000 h storage at ambient environment, and &gt; 90% after 1000 h LED illumination.