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Wound healing is a long-term and complex biological process that involves multiple hemostasis, inflammation, proliferation, and remodeling stages. In order to realize comprehensive and systematic wound management, appropriate wound treatment bio-adhesives are urgently needed. Hydrogel bio-adhesives have excellent properties and show unique and remarkable advantages in the field of wound management. This review begins with a detailed description of the design criteria and functionalities of ideal hydrogel bio-adhesives for wound healing. Then, recent advances in polysaccharide-based multifunctional hydrogel bio-adhesives, which involve chitosan, hyaluronic acid, alginate, cellulose, dextran, konjac glucomannan, chondroitin sulfate, and other polysaccharides, are comprehensively discussed. Finally, the current challenges and future research directions of polysaccharide-based hydrogel bio-adhesives for wound healing are proposed to stimulate further exploration by researchers.

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This study presents large-scale fabrication of singlecrystal SiC nanowire (SiC nw ) sponges through a carbothermal reduction approach using agricultural residue loofah, which is believed to be a perfect alternative to traditional petrochemical materials as the carbon source in industrial fabrication of SiC nanowires, without additional chemical C sources or catalysts. The single-crystal ultralong SiC nw are observed to have diverse morphologies with diameters of 50−400 nm, which possess a significant anisotropic and hierarchical microstructure with planaraligned bamboo joints. A roughly 2 nm thick amorphous SiO 2 layer is identified wrapping the crystalline 3C-SiC. The underlying vapor−solid mechanism is systematically investigated via thermodynamic calculations on the formation and interactions of SiO, CO, and SiC. Noteworthily, the fabricated loofah-based SiC nw sponge exhibits prominent high-temperature performance after thermal insulation tests of alcohol lamp flame and butane blowtorch flame, which is attributed to the stacking faults, SiO 2 layer, SiC/ SiO 2 interface of the nanowires, and the overlength pathway in the porous aerogel−sponge domain synergetically acting as a phonon barrier to enhance phonon scattering, prolong phonon diffusion, and eventually reduce solid thermal conductivity in the sponge architecture. Our current work has great potential to be applied in the eco-friendly industrial preparation of high-performing SiC nw as thermal protection materials in harsh environments.

A series of aggregation-induced emission (AIE)-featured phenylmethylene pyridineacetonitrile derivatives named o-DBCNPy ((Z)-3-(4-(di-p-tolylamino)phenyl)-2-(pyridin-2-yl)acrylonitrile), m-DBCNPy ((Z)-3-(4-(di-p-tolylamino)phenyl)-2-(pyridin-3-yl)acrylonitrile), and p-DBCNPy ((Z)-3-(4-(di-p-tolylamino)phenyl)-2-(pyridin-4-yl)acrylonitrile) have been synthesized by tuning the substitution position of the pyridine ring. The linkage manner of the pyridine ring had influences on the molecular configuration and conjugation, thus leading to different photophysical properties. The absorption and fluorescence emission peak showed a bathochromic shift when the linking position of the pyridine ring changed from the meta to the ortho and para position. Meanwhile, o-DBCNPy exhibited the highest fluorescence quantum yield of 0.81 and the longest fluorescence lifetime of 7.96 ns as a neat film among all three isomers. Moreover, non-doped organic light-emitting diodes (OLEDs) were assembled in which the molecules acted as the light-emitting layer. Due to the relatively prominent emission properties, the electroluminescence (EL) performance of the o-DBCNPy-based OLED was superior to those of the devices based on the other two isomers with an external quantum efficiency (EQE) of 4.31%. The results indicate that delicate molecular modulation of AIE molecules could endow them with improved photophysical properties, making them potential candidates for organic photoelectronic devices.

Using bulk metals as catalysts to get high efficiency in electro-reduction of CO 2 is ideal but challenging. Here, we report the coupling of bulk metal electrodes and a ternary ionic-liquid-based electrolyte, 1-butyl-3-methylimidazolium tetrafluoroborate/1-dodecyl-3-methylimidazolium tetrafluoroborate/MeCN to realize highly efficient electro-reduction of CO 2 to CO. Over various bulk metal electrodes, the ternary electrolyte not only increases the current density but also suppresses the hydrogen evolution reaction to obtain a high Faradaic efficiency (FE) toward CO. FE CO could maintain ∼100% over a wide potential range, and metal electrodes showed very high stability in the ternary electrolyte. It is demonstrated that the aggregation behavior of the ternary electrolyte and the arrangement of two kinds of IL cations with different chain lengths in the electrochemical double layer not only increase the wettability to electrode and CO 2 adsorption but also extend the diffusion channel of H + , rendering the high current density and FE CO .

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