Although electrospinning (e-spinning) has witnessed rapid development in recent years, it has also been criticized by environmentalists due to the use of organic solvents. Therefore, aqueous e-spinning (green e-spinning) is considered a more attractive technique. However, considering the poor water resistance and mechanical properties of electrospun (e-spun) nanofibers, cross-linking is a perfect solution. In this review, we systematically discuss the cross-linking e-spinning system for the first time, including cross-linking strategies (in situ, liquid immersion, vapor, and spray cross-linking), cross-linking mechanism (physical and chemical cross-linking) of e-spun nanofibers, and the various applications (e.g., tissue engineering, drug delivery, water treatment, food packaging, and sensors) of cross-linked e-spun nanofibers. Among them, we highlight several cross-linking methods, including UV light cross-linking, electron beam cross-linking, glutaraldehyde (and other commonly used cross-linking agents) chemical cross-linking, thermal cross-linking, and enzymatic cross-linking. Finally, we confirm the significance of cross-linking e-spinning and reveal the problems in the construction of this system.

This review addresses the applications of electrospinning in the thermal management of polymer matrix composites, mainly involving enhanced thermal conductivity, thermal insulation, and passive daytime radiative cooling.

A novel core–shell-type electrorheological (ER) composite material was fabricated via using polyaniline as an insulating layer to the outer surface of the core conductive metal–organic framework (MIL-125) with controlled size and morphology. MIL-125 was firstly synthesized by a solvothermal method, and then polyaniline was synthesized in a polar solvent and a tight coating was successfully achieved to form a MIL-125@PANI core–shell nanocomposite. This core–shell structure greatly enhances the polarization ability of dispersed particles, thereby improving their rheological properties. The morphology of pure MIL-125 and MIL-125@PANI has been characterized by transmission electron microscopy (TEM) and scanning electron microscopy (SEM). Their structure was characterized by X-ray powder diffraction. Moreover, the ER activity of MIL-125-based and MIL-125@PANI-based ER fluids by dispersing the particles into silicone oil was studied using a rotational rheometer. The results show that the MIL-125@PANI composite particles have higher ER properties.