Explore the vast range of titles available.

•Non-invasive mALPS-index was closely related to the classical detected glymphatic clearance function, providing an alternative method in researches on glymphatic system.•WMHs, lacunas, microbleeds and EPVS in basal ganglia were related to glymphatic clearance function.•Glymphatic clearance function was related to cognitive function in CSVD patients. Few studies have focused on the connection between glymphatic dysfunction and cerebral small vessel disease (CSVD), partially due to the lack of non-invasive methods to measure glymphatic function. We established modified index for diffusion tensor image analysis along the perivascular space (mALPS-index), which was calculated on diffusion tensor image (DTI), compared it with the classical detection of glymphatic clearance function calculated on Glymphatic MRI after intrathecal administration of gadolinium (study 1), and analyzed the relationship between CSVD imaging markers and mALPS-index in CSVD patients from the CIRCLE study (ClinicalTrials.gov ID: NCT03542734) (study 2). Among 39 patients included in study 1, mALPS-index were significantly related to glymphatic clearance function calculated on Glymphatic MRI ( r  = -0.772~-0.844, p < 0.001). A total of 330 CSVD patients were included in study 2. Severer periventricular and deep white matter hyperintensities (β = -0.332, p < 0.001; β = -0.293, p < 0.001), number of lacunas (β = -0.215, p < 0.001), number of microbleeds (β = -0.152, p = 0.005), and severer enlarged perivascular spaces in basal ganglia (β = -0.223, p < 0.001) were related to mALPS-index. Our results indicated that non-invasive mALPS-index might represent glymphatic clearance function, which could be applied in clinic in future. Glymphatic clearance function might play a role in the development of CSVD.

Perovskite solar cells with an inverted architecture provide a key pathway for commercializing this emerging photovoltaic technology because of the better power conversion efficiency and operational stability compared with the normal device structure. Specifically, power conversion efficiencies of the inverted perovskite solar cells have exceeded 25% owing to the development of improved self-assembled molecules 1 – 5 and passivation strategies 6 – 8 . However, poor wettability and agglomeration of self-assembled molecules 9 – 12 cause interfacial losses, impeding further improvement in the power conversion efficiency and stability. Here we report a molecular hybrid at the buried interface in inverted perovskite solar cells that co-assembled the popular self-assembled molecule [4-(3,6-dimethyl-9 H -carbazol-9-yl)butyl]phosphonic acid (Me-4PACz) with the multiple aromatic carboxylic acid 4,4′,4″-nitrilotribenzoic acid (NA) to improve the heterojunction interface. The molecular hybrid of Me-4PACz with NA could substantially improve the interfacial characteristics. The resulting inverted perovskite solar cells demonstrated a record certified steady-state efficiency of 26.54%. Crucially, this strategy aligns seamlessly with large-scale manufacturing, achieving one of the highest certified power conversion efficiencies for inverted mini-modules at 22.74% (aperture area 11.1 cm 2 ). Our device also maintained 96.1% of its initial power conversion efficiency after more than 2,400 h of 1-sun operation in ambient air. High efficiency in perovskite solar cells is achieved by using a molecular hybrid of a self-assembled monolayer with nitrilotribenzoic acid.

The long-term stability of perovskite solar cells remains one of the most important challenges for the commercialization of this emerging photovoltaic technology. Here, we adopt a non-noble metal/metal oxide/polymer multiple-barrier to suppress the halide consumption and gaseous perovskite decomposition products release with the chemically inert bismuth electrode and Al 2 O 3 /parylene thin-film encapsulation, as well as the tightly closed system created by the multiple-barrier to jointly suppress the degradation of perovskite solar cells, allowing the corresponding decomposition reactions to reach benign equilibria. The resulting encapsulated formamidinium cesium-based perovskite solar cells with multiple-barrier maintain 90% of their initial efficiencies after continuous operation at 45 °C for 5200 h and 93% of their initial efficiency after continuous operation at 75 °C for 1000 h under 1 sun equivalent white-light LED illumination. The long-term stability of perovskite solar cells remains a critical challenge for the commercialization of the technology. Here, the authors adopt a non-noble metal/metal oxide/polymer multiple-barrier to suppress device degradation, achieving long-term stability in encapsulated p-i-n devices.

Power conversion efficiencies of inverted perovskite solar cells (PSCs) based on methylammonium- and bromide-free formamidinium lead triiodide (FAPbI 3 ) perovskites still lag behind PSCs with a regular configuration. Here we improve the quality of both the bulk and surface of FA 0.98 Cs 0.02 PbI 3 perovskite films to reduce the efficiency gap. First, we use dibutyl sulfoxide, a Lewis base additive, to improve the crystallinity and reduce the defect density and internal residual stress of the perovskite bulk. Then, we treat the surface of the perovskite film with trifluorocarbon-modified phenethylammonium iodide to optimize the energy levels, passivate defects and protect the film against moisture. The inverted PSCs simultaneously achieve 25.1% efficiency (24.5% from the reverse current–voltage scan measured by a third-party institution) and improved stability. The devices maintained 97.4% and 98.2% of their initial power conversion efficiencies after operating under continuous 1-sun air mass 1.5 G illumination for 1,800 h and under damp heat conditions (85 °C and 85% relative humidity) for 1,000 h, respectively. The efficiency and stability of methylammonium- and bromide-free perovskite inverted solar cells need improvement. Now, Chen et al. combine a Lewis-based additive with a fluorocarbon-modified ammonium salt to reduce defects in the perovskite, increasing the device performance.

Hyperactivation of hypothalamic–pituitary–adrenal (HPA) axis and hypothalamic–pituitary–thyroid (HPT) axis were found in acute high altitude challenge, but the role of gut microbiota and metabolites is unknown. We utilized adult male Sprague–Dawley rats at a simulated altitude of 5500 m for 3 days in a hypobaric-hypoxic chamber. ELISA and metabolomic analyses of serum and 16S rRNA and metabolomic analyses of fecal samples were then performed. Compared with the normoxic group, serum corticotropin-releasing hormone (CRH), adrenocorticotropic hormone (ACTH), corticosterone (CORT), and thyroxine (tT 4 ) were increased in the hypoxia group, whereas thyrotropin-releasing hormone (TRH) was decreased. Bacteroides , Lactobacillus, Parabacteroides, Butyricimonas, SMB53, Akkermansia, Phascolarctobacterium, and Aerococcus were enriched in hypoxia group, whereas [ Prevotella ], Prevotella, Kaistobacter, Salinibacterium, and Vogesella were enriched in normoxic group. Metabolomic analysis indicated that acute hypoxia significantly affected fecal and serum lipid metabolism. In addition, we found five fecal metabolites may mediate the cross-talk between TRH, tT 4 , and CORT with [ Prevotella ], Kaistobacter, Parabacteroides, and Aerococcus , and 6 serum metabolites may mediate the effect of TRH and tT 4 on [ Prevotella ] and Kaistobacter by causal mediation analysis. In conclusion, this study provides new evidence that key metabolites mediate the cross-talk between gut microbiota with HPA and HPT axis under acute hypobaric hypoxia challenge.

All-perovskite tandem solar cells have shown great promise in breaking the Shockley–Queisser limit of single-junction solar cells. However, the efficiency improvement of all-perovskite tandem solar cells is largely hindered by the surface defects induced non-radiative recombination loss in Sn–Pb mixed narrow bandgap perovskite films. Here, we report a surface reconstruction strategy utilizing a surface polishing agent, 1,4-butanediamine, together with a surface passivator, ethylenediammonium diiodide, to eliminate Sn-related defects and passivate organic cation and halide vacancy defects on the surface of Sn–Pb mixed perovskite films. Our strategy not only delivers high-quality Sn–Pb mixed perovskite films with a close-to-ideal stoichiometric ratio surface but also minimizes the non-radiative energy loss at the perovskite/electron transport layer interface. As a result, our Sn–Pb mixed perovskite solar cells with bandgaps of 1.32 and 1.25 eV realize power conversion efficiencies of 22.65% and 23.32%, respectively. Additionally, we further obtain a certified power conversion efficiency of 28.49% of two-junction all-perovskite tandem solar cells. The efficiency of all-perovskite tandem solar cells is impacted by the nonradiative recombination loss in Sn–Pb mixed narrow bandgap perovskite films. Here, the authors utilize a surface polishing agent with surface passivator to deliver films with a close-to-ideal stoichiometric ratio surface.

With a series of widespread applications, resistive gas sensors are considered to be promising candidates for gas detection, benefiting from their small size, ease-of-fabrication, low power consumption and outstanding maintenance properties. One-dimensional (1-D) nanomaterials, which have large specific surface areas, abundant exposed active sites and high length-to-diameter ratios, enable fast charge transfers and gas-sensitive reactions. They can also significantly enhance the sensitivity and response speed of resistive gas sensors. The features and sensing mechanism of current resistive gas sensors and the potential advantages of 1-D nanomaterials in resistive gas sensors are firstly reviewed. This review systematically summarizes the design and optimization strategies of 1-D nanomaterials for high-performance resistive gas sensors, including doping, heterostructures and composites. Based on the monitoring requirements of various characteristic gases, the available applications of this type of gas sensors are also classified and reviewed in the three categories of environment, safety and health. The direction and priorities for the future development of resistive gas sensors are laid out.

This study proposes a novel method to address the instability issues in multi-target bearing-only tracking for passive sonar systems. Utilizing a particle filter-guided on-site training mechanism, the complex multi-classification task is simplified into binary classification (target vs. non-target) by assigning an independent tracker to each target. This enables simultaneous on-site training and deployment of the neural network for tracking. A hybrid CNN-BiLSTM network is constructed: the Convolutional Neural Network (CNN) enhances target feature extraction and non-target discrimination, while the Bidirectional Long Short-Term Memory (BiLSTM) models spatiotemporal dependencies. Their synergy improves trajectory continuity and smoothness. Under simulated conditions, the proposed method reduces the minimum required SNR for stable tracking to −31.78 dB, a significant improvement over the −29.69 dB required by pure particle filtering methods. The average tracking error is also reduced from 0.61° to 0.34°. Both simulations and sea trial data demonstrate that the method maintains stable tracking even during target trajectory crossings, significantly enhancing multi-target tracking accuracy in complex underwater acoustic environments.

β-catenin is an important regulator of malignant progression. 17β-Estradiol (E2), an important sex hormone in women, promotes the growth and metastasis of triple-negative breast cancer (TNBC). However, whether β-catenin is involved in E2-induced metastasis of TNBC remains unknown. In this study, we show that E2 induces the proliferation, migration, invasion, and metastasis of TNBC cells. E2 induces β-catenin protein expression and nuclear translocation, thereby regulating the expression of target genes such as Cyclin D1 and MMP-9. The inhibition of β-catenin reversed the E2-induced cell malignant behaviors. Additionally, E2 activated Calpain by increasing intracellular Ca 2+ levels and reducing calpastatin levels. When Calpain was inhibited, E2 did not induce the proliferation, migration, invasion, or metastasis of TNBC cells. In addition, E2 promoted translocation of YAP into the nucleus by inhibiting its phosphorylation. Calpain inhibition reversed the E2-induced YAP dephosphorylation. Inhibition of YAP transcriptional activity reversed the effects of E2 on the proliferation, migration, invasion, and β-catenin of TNBC cells. In conclusion, we demonstrated that E2 induced metastasis-related behaviors in TNBC cells and this effect was mediated through the Calpain/YAP/β-catenin signaling pathway.

The employment of self-assembled molecular hybrid could improve buried interface in perovskite solar cells (PSCs). However, the interplay among hybrid self-assembled monolayers (SAMs) during the deposition process has not been well-studied. Herein, we study the interaction between co-adsorbents and commonly used SAM material, [4-(3,6-dimethyl-9 H -carbazol-9-yl)butyl]phosphonic acid (Me-4PACz) for wide-bandgap (WBG) PSCs. It is found that the co-adsorbent, 6-aminohexane-1-sulfonic acid (SA) tends to fill the uncovered sites without interference with Me-4PACz, ensuring the formation of a dense hole selective layer. Moreover, the use of SA/Me-4PACz mixed SAMs could effectively reduce the interfacial non-radiative recombination loss, optimize the energy alignment at the buried interface and regulate the crystallization of WBG perovskite. As a result, the 1.77 eV WBG PSCs deliver a power conversion efficiency (PCE) of 20.67% (20.21% certified) and an impressive open-circuit voltage ( V OC ) of 1.332 V (1.313 V certified). By combining with a 1.26 eV narrow-bandgap (NBG) PSC, we further fabricate 2-terminal all-perovskite tandem solar cells (TSCs) with a PCE of 28.94% (28.78% certified) for 0.087 cm 2 and 23.92% for mini-module with an aperture area of 11.3 cm 2 . The interplay among hybrid self-assembled monolayers (SAMs) during deposition has not been well studied. Here, authors mix co-adsorbents with carbazole-based SAM material to improve the buried interface, achieving efficiency of 20.67% for wide-bandgap solar cells and 28.94% for all-perovskite tandem devices.