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Objective: Cardiovascular disease (CVD) represents the primary cause of mortality in patients afflicted with end-stage renal disease and undergoing peritoneal dialysis (PD) treatment. Galectin-3 (Gal-3), a molecule known to exhibit a correlation with CVD mortality garners considerable interest. The objective of this study was to explore the potential association between serum Gal-3 levels and other CVD risk factors among PD patients. Methods: In this cross-sectional study, a total of 114 PD patients with a minimum of 3 months of PD treatment were enrolled. Serum Gal-3 levels were quantified using an enzyme-linked immunosorbent assay. The data of patients with Gal-3 levels higher and lower than 26.744 pg/ml were compared using Mann–Whitney U tests or t tests. Pearson's correlation or Spearman's correlation analysis and multivariate regression were used to assess the associations between the known risk factors for CVD and Gal-3. Results: In comparison to the inter-group baseline data, the low Gal-3 group exhibited a higher glomerular filtration rate (GFR). Gal-3 levels correlate positively with PD duration, B-type natriuretic peptide (BNP), growth differentiation factor 15 (GDF-15), interventricular septal thickness in diastolic (IVST), and left ventricular mass index (LVMI). Conversely, Gal-3 exhibited a negative correlation with albumin levels. Multivariate linear regression analysis demonstrated a positive correlation between Gal-3 levels and BNP, GDF-15, PD duration, IVST and LVMI. Gal-3 levels were negatively correlated with albumin levels. Conclusions: Gal-3 was strongly associated with BNP, GDF-15, IVST and LVMI in patients undergoing PD treatment. Prospective studies should be carried out to determine whether Gal-3 can be a promising biomarker in predicting increased risk of adverse cardiovascular events in PD patients. [ABSTRACT FROM AUTHOR]

The polymerization of fused-ring acceptors (FRAs) to afford their corresponding polymeric acceptors for high-performance all-polymer solar cells (all-PSCs) has achieved remarkable progress in the past few years. However, due to the high degree of synthetic complexity for the monomer, the high-cost of these polymeric acceptors may limit their commercial applications. Thus, it is urgent to develop inexpensive and high-performance polymeric acceptors for all-PSCs. Herein, two novel polymeric acceptors (PBTzO and PBTzO-2F) have been designed and synthesized by copolymerization of noncovalently fused ring acceptors (NFRAs), which were employed in all-PSCs for the first time. Upon introducing the "noncovalently conformational locks (NoCLs)" in the backbone and selective fluorination of the end-group, photophysical and electrical properties, and solid-state packing properties of the NFRAs have been rationally tuned. As a result, the PBDB-T:PBTzO-2F based devices presented an excellent power conversion efficiency (PCE) of 11.04%, much higher than that of PBTzO based ones due to the increased charge generation and extraction, improved hole transfer and carrier mobilities, and reduced energy loss. More importantly, PBTzO-2F exhibited a much lower synthetic complexity (SC) index and higher figure-of-merit (FOM) values than the highperformance fused-ring acceptor based polymer acceptors (FRA-PAs) due to the simpler structures and more effective synthesis. This contribution provided a novel idea to achieve low-cost and high-performance all-PSCs. [ABSTRACT FROM AUTHOR]

Solid-state refrigeration based on the caloric effect is viewed as a promising efficient and clean refrigeration technology. Barocaloric materials were developed rapidly but have since encountered a general obstacle: the prominent caloric effect cannot be utilized reversibly under moderate pressure. Here, we report a mechanism of an emergent large, reversible barocaloric effect (BCE) under low pressure in the hybrid organic–inorganic layered perovskite (CH3–(CH2)n−1–NH3)2MnCl4 (n = 9,10), which show the reversible barocaloric entropy change as high as ΔSr ∼ 218, 230 J kg−1 K−1 at 0.08 GPa around the transition temperature (Ts ∼ 294, 311.5 K). To reveal the mechanism, single-crystal (CH3–(CH2)n−1–NH3)2MnCl4 (n = 10) was successfully synthesized, and high-resolution single-crystal X-ray diffraction (SC-XRD) was carried out. Then, the underlying mechanism was determined by combining infrared (IR) spectroscopy and density function theory (DFT) calculations. The colossal reversible BCE and the very small hysteresis of 2.6 K (0.1 K/min) and 4.0 K (1 K/min) are closely related to the specific hybrid organic–inorganic structure and single-crystal nature. The drastic transformation of organic chains confined to the metallic frame from ordered rigidity to disordered flexibility is responsible for the large phase-transition entropy comparable to the melting entropy of organic chains. This study provides new insights into the design of novel barocaloric materials by utilizing the advantages of specific organic–inorganic hybrid characteristics.Solid-state coolants: Hybrid crystals deliver big chills at low pressures Materials that can absorb and release heat under low mechanical pressure hold promise for high-efficiency refrigeration technology. Recent studies have shown that significant compression-induced cooling effects at low pressures can be achieved using crystals known as perovskites containing layers of organic chains and metal cations. Yihong Gao from the Chinese Academy of Sciences in Beijing and colleagues have now uncovered the mechanism underlying the thermal response of layered perovskites. Using a combination of x-rays, spectroscopy and theoretical calculations, the team discovered how the crystal structure changes at different temperatures. Their experiments revealed a low-energy phase transition where organic chains transform from rigid states to highly flexible conformations held in place by metallic layers. The large entropy change associated with this transition and its reversible nature could aid in the design of other organic–inorganic solid-state coolants.For the emergent colossal, reversible barocaloric effect in organic–inorganic perovskite hybrids (CH3–(CH2)n−1–NH3)2MnCl4 (n = 9, 10), we successfully grew a single crystal, and the underlying mechanism was determined by high-resolution SC-XRD, IR spectroscopy and DFT calculations. The drastic transformation of organic chains confined to the metallic frame from ordered rigidity to disordered flexibility is responsible for the large phase-transition entropy, which is comparable to the melting entropy of organic chains. The result provides new insights into designing novel barocaloric materials by utilizing the disordering of organic chains of organic–inorganic hybrid materials. [ABSTRACT FROM AUTHOR]

In recent years, power conversion efficiency (PCE) of organic solar cells (OSCs) has made significant improvement. A large number of studies were reported to achieve high PCEs through exploring new active layer materials, especially the high efficiency fused ring acceptors (FRAs). Compared with FRAs, another type of so-called unfused-ring acceptors (UFAs), possessing some advantages such as simple synthesis and low cost, have attracted a lot of attention. Herein, a new UFA BTzO-4F, incorporating with a benzotriazole moiety and S⋯O intramolecular noncovalent interactions, has been successfully synthesized. The photovoltaic device based on PBDB-T:BTzO-4F achieved a record PCE of 13.8% for UFAs, which indicates that introducing the benzotriazole moiety is an effective strategy for high quality acceptors. Thus, these findings of this work demonstrate the great potential of UFAs for high performance OSCs. [ABSTRACT FROM AUTHOR]

AgWO/g-CN composites with different AgWO concentration and calcination temperature were synthesized via a mixing and heating approach. Various techniques were used to investigate the characters of the as-prepared samples, such as thermogravimetric analysis, X-ray diffraction, Fourier transform infrared spectroscopy, UV-Vis diffuse reflectance spectroscopy, X-ray photoelectron spectroscopy, scanning electron microscopy, transmission electron microscopy and photoluminescence spectroscopy. The degradation of rhodamine B (20 ppm) under visible light was performed to investigate the photocatalytic activity of AgWO/g-CN composites. Results indicate that the AgWO/g-CN is actually Ag/AgWO/g-CN ternary system. 7.5 wt% AgWO/g-CN prepared at 300 °C presented the best photocatalytic performance in rhodamine B degradation. The degradation rate reaches 0.0679 min, which is 3.25 times higher than the value of pure g-CN. The enhanced activity is attributed to the synergetic effect of AgWO, g-CN and metal Ag. Additionally, cycling experiments also proved that the AgWO/g-CN photocatalyst has good stability. [ABSTRACT FROM AUTHOR]