The emerging solar desalination technology is considered as one of the most promising strategies to ensure water security. However, with the proceeding of solar desalination, salt crystallization on the surface of solar evaporators caused by increasing salinity of seawater will result in a decrease in the evaporation rate. Thus, it is still challenging to fabricate solar evaporators with superior salt resistance. In this work, elastic ceramic‐based nanofibrous aerogels with a cellular architecture are fabricated by the combination of electrospinning and fiber freeze‐shaping technologies, which are composed of vertically aligned vessels and porous vessel walls. Under the action of convection and diffusion promoted by this unique cellular architecture, the aerogels exhibit a superior salt‐resistance without any salt crystals on the surface of aerogels even in 20% brine and under 6‐sun irradiation. Moreover, by virtue of the synergistic effect of the promising structure and light absorbance of carbon nanotubes, aerogels possess a high light absorbance of up to 98% and excellent evaporation performance achieving 1.50 kg m−2 h−1 under 1‐sun irradiation. This work may provide a fascinating avenue for the desalination of seawater in a salt‐resistance and efficient manner.

Over the past several decades, we have witnessed significant progress in chitosan and chitin based nanostructured materials. The nanofibers from chitin and chitosan with appealing physical and biological features have attracted intense attention due to their excellent biological properties related to biodegradability, biocompatibility, antibacterial activity, low immunogenicity and wound healing capacity. Various methods, such as electrospinning, self-assembly, phase separation, mechanical treatment, printing, ultrasonication and chemical treatment were employed to prepare chitin and chitosan nanofibers. These nanofibrous materials have tremendous potential to be used as drug delivery systems, tissue engineering scaffolds, wound dressing materials, antimicrobial agents, and biosensors. This review article discusses the most recent progress in the preparation and application of chitin and chitosan based nanofibrous materials in biomedical fields.

The regeneration of bone tissue is regulated by both osteogenic and angiogenic growth factors which are expressed in a coordinated cascade of events. The aim of this study was to create a dual growth factor-release system that allows for time-controlled release to facilitate bone regeneration. We fabricated core−shell SF/PCL/PVA nanofibrous mats using coaxial electrospinning and layer-by-layer (LBL) techniques, where bone morphogenetic protein 2 (BMP2) was incorporated into the core of the nanofibers and connective tissue growth factor (CTGF) was attached onto the surface. Our study confirmed the sustained release of BMP2 and a rapid release of CTGF. Both in vitro and in vivo experiments demonstrated improvements in bone tissue recovery with the dual-drug release system. In vivo studies showed improvement in bone regeneration by 43% compared with single BMP2 release systems. Time-controlled release enabled by the core−shell nanofiber assembly provides a promising strategy to facilitate bone healing.

Complex structured soft matter may have important applications in the field of tissue engineering and biomedicine. However, the discovery of facile methods to exquisitely manipulate the structure of soft matter remains a challenge. In this report, a multilayer hydrogel is fabricated from the stimuli-responsive aminopolysaccharide chitosan by using spatially localized and temporally controlled sequences of electrical signals. By programming the imposed cathodic input signals, chitosan hydrogels with varying layer number and thickness can be fabricated. The inputs of electrical signals induce the formation of hydrogel layers while short interruptions create interfaces between each layer. The thickness of each layer is controlled by the charge transfer (Q = ∫idt) during the individual deposition step and the number of multilayers is controlled by the number of interruptions. Scanning electron micrographs (SEMs) reveal organized fibrous structures within each layer that are demarcated by compact orthogonal interlayer structures. This work demonstrates for the first time that an imposed sequence of electrical inputs can trigger the self-assembly of multilayered hydrogels and thus suggests the broader potential for creating an electrical "code" to generate complex structures in soft matter.

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Natural polymeric hydrogels with self-healing capability that can recover the functionalities and structures of gels after damage are extremely attractive due to their emerging applications in the biomedical field. Here we report a self-healable polymeric hydrogel by self-crosslinking two natural polymers acrylamide-modified chitin (AMC) containing amino groups and oxidized alginate containing dialdehyde groups. The generation of the self-crosslinked hydrogel relies on the dynamic covalent linkage through Schiff base between the polysaccharide chains. The self-healing capability of the crosslinked hydrogel depends on the molar ratio of AMC and oxidized alginate and the surrounding pH. Under certain circumstances, the damaged hydrogel shows a complete recovery and can be stretched to a favorable extent, which is seldom observed for polysaccharide self-healing hydrogel. Notably, we find that the self-healing ability can be "stored" by freeze-drying and "activated" by rehydration. In addition, we demonstrate that the hydrogel can be used as a soft template to guide the repair of inorganic materials like hydroxyapatite. We anticipate that this self-healable hydrogel consisting of biocompatible and biodegradable polysaccharides can be applied to various biomedical fields.

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Sufficient and clean freshwater is still out of reach for billions of people around the world. Solar desalination from brine is regarded as one of the most promising proposals to solve this severe crisis. However, most of the reported evaporators to date still suffer from the decreasing evaporation rate caused by salt crystallization accumulated on their surface. Here, inspired by the vascular tissue structure, transpiration, and antifouling function of reed leaves, we design biomimetic hierarchical nanofibrous aerogels with parallel-arranged vessels and hydrophobic surfaces for highly efficient and salt-resistant solar desalination. Foldable vessel walls and flexible silica nanofibers give the reed leaf-inspired nanofiber aerogels (R-NFAs) excellent mechanical properties and enable them to withstand repeated compression. Besides, the R-NFAs can efficiently absorb sunlight (light absorption efficiency: 94.8%) and evaporate the brine to vapor, similar to reed leaves (evaporation rate: 1.25 kg m −2 h −1 under 1 sun). More importantly, enabled by the hydrophobic surfaces and parallel-arranged vessels, the R-NFAs can work stably in high-concentration brine (saturated, 26.3 wt %) under high-intensity light (up to 6 sun), demonstrating potent salt resistance. It is expected that R-NFAs with combined antisalt pore and surface structures will provide a designed concept for salt-resistant solar desalination.