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Directional freeze-drying is considered to regulate the structure of nanocellulose aerogels with special performances. In this work, TEMPO-oxidized cellulose nanofiber aerogels with high porosity (> 99.5%) and low density (~ 7 mg/cm3) were produced by different freeze-drying methods. The effects of temperature, freezing reagents and freezing methods on the structure and properties of aerogels were investigated. Among them, an anisotropic cellulose aerogel was obtained using a simple and flexible directional freezing in ethanol of − 30 °C by a self-made directional freezer. Our results demonstrated that it could present honeycomb-like pores in the transverse direction and regular directional tunnels in the longitudinal direction, and some attractive features, such as high water adsorption (120 g/g) and stability in water. Compared with other aerogels, this anisotropic structure also provided the aerogel with excellent compressive property (15.2 kPa) and faster liquid transport (4.95 mm/s) in the longitudinal direction than in other directions. The distinctive aerogels based on nanocellulose by directional freeze-drying are also expected to be combined with multifunctional materials to achieve directional applications to meet the requirements of different fields. [ABSTRACT FROM AUTHOR]

Nanocellulose, as a nanoscale polymer material, has garnered significant attention worldwide due to its numerous advantages including excellent biocompatibility, thermal stability, non-toxicity, large specific surface area, and good hydrophilicity. Various methods can be employed for the preparation of nanocellulose. Traditional approaches such as mechanical, chemical, and biological methods possess their own distinct characteristics and limitations. However, with the growing deterioration of our living environment, several green and environmentally friendly preparation techniques have emerged. These novel approaches adopt eco-friendly technologies or employ green reagents to achieve environmental sustainability. Simultaneously, there is a current research focus on optimizing traditional nanocellulose preparation methods while addressing their inherent drawbacks. The combination of mechanical and chemical methods compensates for the limitations associated with using either method alone. Nanocellulose is widely used in wound dressings owing to its exceptional properties, which can accelerate the wound healing process and reduce patient discomfort. In this paper, the principle, advantages and disadvantages of each preparation method of nanocellulose and the research findings in recent years are introduced Moreover, this review provides an overview of the utilization of nanocellulose in wound dressing applications. Finally, the prospective trends in its development alongside corresponding preparation techniques are discussed. [ABSTRACT FROM AUTHOR]

Stretchable electroluminescent (EL) devices show great potential for wearable displays. However, the integration of stretchability, flexibility, temperature-tolerance, waterproofness and biocompatibility into a single EL device remains a challenge. Herein, we report a facile full solution-process method for a novel EL device consisting of a dielectric luminescent layer sandwiched between two silver nanowires-cellulose nanocrystals with II crystalline allomorphs/polydopamine-polydimethylsiloxane (CNC II-AgNWs/PDA-PDMS) electrodes. CNC II is used as a green dispersant, film-forming agent and antioxidant to improve the optical, electrical, mechanical and antioxidant properties of the electrodes. The electrodes exhibit a smooth surface, low sheet resistance (~11 Ω sq−1), high transparency (~79.2 %), ideal stretchability (~100 % strain) and excellent inoxidizability. The assembled EL devices with outstanding tensile stability and fatigue resistance demonstrate excellent luminance, flexibility and stretchability underwater and at extreme temperatures, as well as intrinsic biocompatibility. Our multifunctional EL devices with outstanding integrated properties provide new insights for the next-generation flexible electronics. [Display omitted] [ABSTRACT FROM AUTHOR]