Alginate based films integrated with nitrogen-functionalized carbon dots and layered clay for active food packaging applications.

The applications of alginate derived from seaweed polysaccharide in food packaging are restricted due to their inherent deficient antibacterial, antioxidant and UV barrier properties. In this study, nitrogen-functionalized carbon dots (NCDs) with active functions (0.5-3 %) and layered clay (1 %) with barrier property were introduced to construct alginate based active films via solution casting method. The results showed that the synthesized spherical NCDs had a particle size of 2-3 nm, and the internal structure of NCDs was similar to graphene, with a large number of active groups (-NH2, -OH, etc.) on the surface. Infrared analysis revealed that NCDs could form strong hydrogen bonds with alginate matrix, which slowed down the deterioration of mechanical properties and reduced the surface wettability. With the addition of NCDs, active functions and surface hydrophobicity of the active films were enhanced significantly (P < 0.05). When the amount of NCDs reached 3 %, UV barrier, antioxidant and antibacterial properties of the active films were increased by 50.0 %, 61.1 % and 70.1 %, respectively. The addition of NCDs could enhance the anti-browning ability of alginate based coatings and extend the shelf life of banana significantly. Therefore, a suitable amount of NCDs (1-2 %) and layered clay (1 %) can synergistically improve comprehensive performance of alginate based films and promote their food packaging application used as active films/inner coatings.

MAVI1, an endoplasmic reticulum-localized microprotein, suppresses antiviral innate immune response by targeting MAVS on mitochondrion.

Pattern recognition receptor-mediated innate immunity is critical for host defense against viruses. A growing number of coding and noncoding genes are found to encode microproteins. However, the landscape and functions of microproteins in responsive to virus infection remain uncharacterized. Here, we systematically identified microproteins that are responsive to vesicular stomatitis virus infection. A conserved and endoplasmic reticulum-localized membrane microprotein, MAVI1 (microprotein in antiviral immunity 1), was found to interact with mitochondrion-localized MAVS protein and inhibit MAVS aggregation and type I interferon signaling activation. The importance of MAVI1 was highlighted that viral infection was attenuated and survival rate was increased in Mavi1-knockout mice. A peptide inhibitor targeting the interaction between MAVI1 and MAVS activated the type I interferon signaling to defend viral infection. Our findings uncovered that microproteins play critical roles in regulating antiviral innate immune responses, and targeting microproteins might represent a therapeutic avenue for treating viral infection.

Metal-organic framework derived bimetal oxide CuCoO2 as efficient electrocatalyst for the oxygen evolution reaction.

Metal-organic framework (MOF) materials with tunable porous morphology, controlled crystalline structure, various compositions, and high specific surface area are widely used as precursors to synthesize electrocatalysts for water splitting, which is beneficial for improving their oxygen evolution reaction (OER) performance. Using ZIF-67 as a Co source and Cu-BTC as a Cu source, hexagonal MOF-derived CuCoO2 (MOF-CCO) nanocrystals with the size of ∼288 nm were prepared through a one-step solvothermal method. The influence of the content of the precursor solvents (absolute ethanol and deionized water), reaction temperature, mass ratio of reactants, NaOH addition, and reactant concentration of precursors on the structure and morphology of the products was investigated. The optimal CuCoO2 nanocrystals (MOF-CCO1) around 288 nm present the highest OER activity, such as a low overpotential of 364.7 mV at 10 mA cm-2, a small Tafel slope of 64.1 mV dec-1, and attractive durability in 1.0 M KOH solution. The XPS results showed that the higher catalytic efficiency of MOF-CCO1 nanocrystals could be due to the oxygen vacancies caused by lattice oxygen loss, the increase of OH- content on the surface, and the synergistic effect of Cu2+/Cu+ and Co2+/Co3+ redox pairs. Finally, a possible OER mechanism for MOF-CCO nanocrystals of water splitting was proposed. This study provides a new approach for the preparation of delafossite nanomaterials and for the improvement of their OER performances.

Hydrothermal synthesized delafossite CuGaO2 as an electrocatalyst for water oxidation.

Hydrogen production from water splitting provides an effective method to alleviate the ever-growing global energy crisis. In this work, delafossite CuGaO2 (CGO) crystal was synthesized through hydrothermal routes with Cu(NO3)2·3H2O and Ga(NO3)3·xH2O used as reactants. The addition of cetyltrimethylammonium bromide (CTAB) was found to play an important role in modifying the morphology of CuGaO2 (CGO-CTAB). With the addition of CTAB, the morphology of CGO-CTAB samples changed from irregular flake to typical hexagonal sheet microstructure, with an average size of 1-2 µm and a thickness of around 100 nm. Furthermore, the electrocatalytic activity of CGO-CTAB crystals for oxygen evolution reaction (OER) was also studied and compared with that of CGO crystals. CGO-CTAB samples exhibited better activity than CGO. An overpotential of 391.5 mV was shown to be able to generate a current density of 10 mA/cm2. The as-prepared samples also demonstrate good stability for water oxidation and relatively fast OER kinetics with a Tafel slope of 56.4 mV/dec. This work highlights the significant role of modification of CTAB surfactants in preparing CGO related crystals, and the introduction of CTAB was found to help to improve their electrocatalytic activity for OER.