The vitrification of embryos is essential for animal reproduction and significantly contributes to assisted reproductive technologies, enabling fast cryopreservation without ice crystal formation. Mitochondria, vital organelles in cellular metabolism, are responsible for critical functions like ATP synthesis, calcium regulation, and apoptotic signaling. Preserving mitochondrial integrity is essential for ensuring embryonic strength. Studies demonstrate that vitrification, a widely used cryopreservation method, can markedly impair mitochondrial function in mammalian embryos. This study examines the efficacy of novel/modified antifreeze peptide as a biocompatible agent when used in an appropriate concentration with base vitrification media. Blastocysts vitrified in base media as well as supplemented with the peptide exhibited significantly enhanced post-thaw survival rates, attaining re-expansion and hatching rates of 96.89 ± 4.2% and 88.31 ± 1.3%, respectively, in contrast to 79.38 ± 3.7% and 52.57.9 ± 0.8% observed in the control group. Furthermore, peptide-treated BLs demonstrated elevated expression of PGC1α, BCL2, and Sirt-1, which are the key genes related to mitochondrial membrane potential and anti-apoptotic factors. The mitochondrial function was maintained, and the levels of reactive oxygen species (ROS) and the expression of genes such as Cyto-c, caspases 3, and caspase 9 were markedly diminished in the embryos vitrified with peptide. These findings highlight the ability of this modified peptide to preserve mitochondrial integrity and reduce oxidative stress, hence enhancing the survival of blastocysts post-vitrification.

The lactic acid bacteria, Lactiplantibacillus plantarum KU15149 and Levilactobacillus brevis KU15176 were verified through phenotypic and genotypic analyses. Safety evaluation was conducted using multiple assays, including minimum inhibitory concentration assay for nine antibiotics, hemolytic activity, mucin degradation, gelatin liquefaction, urease activity, indole production, β-glucuronidase activity, bile salt deconjugation, cell cytotoxicity, D-/L-lactic acid production, and biogenic amine formation. Genotypically L. plantarum KU15149 and L. brevis KU15176 lacked all virulence and antibiotic resistance genes investigated. Consistent with these results, phenotypic assays showed that both strains were susceptible according to EFSA cut-off values and tested negative for hemolysis, mucin degradation, gelatin liquefaction, urease activity, indole production, β-glucuronidase activity, and bile salt deconjugation. Furthermore, neither strain showed cytotoxicity toward Caco-2 cells at a multiplicity of infection of 250. Production of D-lactic acid and biogenic amines was negligible in both bacteria. Overall, L. plantarum KU15149 and L. brevis KU15176 demonstrated safety and beneficial characteristics and therefore could serve as probiotic strains.

Covalent organic framework (COF) membranes have emerged as promising candidates for hydrogen purification due to their tunable pore sizes and robust structures. However, achieving high selectivity and permeability simultaneously remains a challenge due to the inherent pore size distribution of COF materials. In this study, we fabricated two distinct COF membranes, TpPa-1 and TpTGCl, with pore sizes of 1.8 nm and 0.39 nm, respectively, using tailored synthesis methods. The TpTGCl membrane, synthesized via room temperature interfacial polymerization and vacuum-assisted filtration, exhibits an ultrathin nanosheet structure with an interlayer π–π stacking distance of 0.33 nm. This unique architecture, combined with its affinity for CO2 adsorption, enables exceptional hydrogen separation performance, achieving a H2/ CO2 selectivity of 52.5 and a H2 permeability of 3.49 × 10– 7 mol m− 2 s− 1 Pa− 1. Molecular dynamics simulations confirmed the steric hindrance effect as the primary mechanism for the selective permeation of hydrogen. The TpTGCl membrane effectively sieves larger gas molecules ( CO2, N2, CH4, etc.) without the need for material modification or excessive membrane thickness. This study demonstrates the potential of COF membranes with tailored pore sizes for high-performance hydrogen purification and offers valuable insights for the development of advanced separation technologies.

Currently, carbon nanotubes (CNTs) paper (also called Buckypaper, BP) is highly promising for application in flexible electronic materials. However, the lack of flexibility and durability of BP greatly affects the comprehensive performance. Here, we propose a simple method for manufacturing a waterborne polyurethane (WPU) toughened carbon nanotube paper (WPU-BP) with excellent overall performance through vacuum filtration. In WPU-BP, as the content of WPU increased from 0 to 48.3%, the tensile strength increased from 8.08 to 16.25 MPa, and the elongation at break increased from 2.14 to 225.04%, while the conductivity decreased from 41.34 to 20.33 S/cm. The WPU-BP with the WPU content of 18.9% (CNP8) demonstrated the optimum strain sensing performance. The gauge factor of CNP8 can reach 8.57 with a response time of 145 ms. It can detect a wide range of body movements from large joint movements to slight breathing, and exhibits high stability, maintaining high stability even after 1000 cycles. In addition, CNP8 shows excellent Joule heating performance, it can reach 186.1 °C at 5 V, with heating and cooling times of only 16 and 18 s, respectively, as well as with good reproducibility. In a word, the as-prepared WPU-BP exhibits excellent both strain sensing performance and Joule heating effect, and holds significant potential for applications in heating devices and wearable sensors.

Waste utilization is not only a way to protect the environment and realize green chemistry, but also a means to create novel materials. In this study, based on waste grape seeds as the biowaste-derived carbon dots (G-BCDs), a straightforward one-pot green method was employed for the rapid detection of folic acid (FA). Owing to the internal filter effect and the static mixing quenching mechanism, the sensing principle of G-BCDs was effectively quenched by FA. The results showed fluorescence at an emission wavelength of 415 nm upon excitation at 330 nm with a quantum yield of 1.5%. Particularly, the FA sensing assay obtained a broad linear range of 2–220 μM and the limit of detection was 0.48 μM. In addition, the fluorescence probe was successfully utilized for detecting FA in tablets, blood, and urine samples, yielding desirable results, which indicated promising applications in the fields of biological and pharmaceutical analysis.

Manganese dioxide, functioning as a cathode material for aqueous zinc-ion batteries (AZIBs), demonstrates a variety of benefits, such as elevated theoretical specific capacity, outstanding electrochemical performance, environmental compatibility, ample resource availability, and facile modification. These advantages make MnO2 one of the cathode materials that have attracted much attention for AZIBs. Nevertheless, manganese dioxide cathode in practical applications suffers from structural instability during the cycling process because of sluggish electrochemical kinetics and volume expansion, which hinder their large-scale application. Doping and compositing with conducting frameworks is an effective strategy for improving structural stability. Herein, homogeneously in situ growth of Yttrium-doped MnO2 nanorods on conductive reduced graphene oxide (Y-MnO2/rGO), were synthesized through a straightforward hydrothermal method. The Y-MnO2/rGO electrodes have an ultra-long cycle life of 179.2 mA h g− 1 after 2000 cycles at 1 A g− 1 without degradation. The excellent structural stability is attributed to the cooperative effect of yttrium doping and compositing with rGO, which is an effective approach to enhance the stability and mitigate the Jahn–Teller distortion associated with Mn ions.

To optimize the electrochemical properties of Ni-rich cathode materials, CPAN@SC-NCM811 is prepared via surface modification of single-crystalline LiNi0.8Co0.1Mn0.1O2 cathode material by adding 1, 2 and 3 wt.% of polyacrylonitrile, respectively. Significantly, the results obtained from X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), field emission scanning electron microscopy (FESEM), and transmission electron microscopy (TEM) verify the successful synthesis of CPAN@SC-NCM811 cathode, which exhibits better electrochemical properties compared to SC-NMC811. After thorough milling and calcination of 2 wt.% polyacrylonitrile with SC-NCM811, the initial discharge specific capacity of prepared S2 sample is 197.7 mAh g− 1 and the capacity retention reached 89.2% after 100 cycles at a rate of 1.0 C. Furthermore, the S2 sample exhibits superior rate performance compared to the other three samples, in which these superior electrochemical properties are largely attributed to the optimal ratio of conductive cyclized polyacrylonitrile coatings. Overall, this work offers guidelines for modifying the surface of SC-NCM811 cathode materials for lithium-ion batteries with exceptional cycling and rate performance.

In recent years, there has been growing interest in the potential applications of carbon-based non-metallic catalysts in various fields, such as electrochemical energy storage, electrocatalysis, thermal catalysis, and photocatalysis, owing to their unique physical and chemical properties. Modifying carbon catalyst surfaces or incorporating non-metallic heteroatoms, such as nitrogen (N), phosphorus (P), boron (B), and sulfur (S), into the carbon structure has emerged as a promising approach to improve the catalytic performance. This method enables the adjustment of the electronic structure of the carbon catalyst's surface, leading to the formation of new active sites or the reduction of side reactions, ultimately enhancing the catalyst's performance. Here, the preparation methods for doped non-metallic heteroatom carbon catalysts have been systematically explored, encompassing techniques, such as impregnation, pyrolysis, chemical vapor deposition (CVD), and templating. Finally, the existing challenges in the application of non-metallic atomic catalysts have been discussed, insights into potential future development opportunities and new preparation methods of carbon catalysts in the future have been offered.