Utilization of self‐healing chemistry to develop synthetic polymer materials that can heal themselves with restored mechanical performance and functionality is of great interest. Self‐healable polymer elastomers with tunable mechanical properties are especially attractive for a variety of applications. Herein, a series of urea functionalized poly(dimethyl siloxane)‐based elastomers (U‐PDMS‐Es) are reported with extremely high stretchability, self‐healing mechanical properties, and recoverable gas‐separation performance. Tailoring the molecular weights of poly(dimethyl siloxane) or weight ratio of elastic cross‐linker offers tunable mechanical properties of the obtained U‐PDMS‐Es, such as ultimate elongation (from 984% to 5600%), Young's modulus, ultimate tensile strength, toughness, and elastic recovery. The U‐PDMS‐Es can serve as excellent acoustic and vibration damping materials over a broad range of temperature (over 100 °C). The strain‐dependent elastic recovery behavior of U‐PDMS‐Es is also studied. After mechanical damage, the U‐PDMS‐Es can be healed in 120 min at ambient temperature or in 20 min at 40 °C with completely restored mechanical performance. The U‐PDMS‐Es are also demonstrated to exhibit recoverable gas‐separation functionality with retained permeability/selectivity after being damaged.

Efficiency, cost, and lifetime are the primary challenges for stationary energy storage with vanadium-redox flow and sodium-sulfur batteries as promising options. In particular, room temperature sodium-sulfur battery systems offer the potential for safe, simple, low-cost and high energy density storage, but the high reactivity or solubility of sodium polysulfides in common liquid electrolytes for carbonates or glycols, respectively, leads to rapid performance loss on cycling. Herein, we demonstrate a robust route to mostly inhibit reactivity of the sulfides with carbonate electrolytes (and also inhibit the diffusion of polysulfides

A nitrogen-doped carbonized metal–organic framework was utilized for room temperature sodium sulfur batteries. The cZIF-8/S composite electrode exhibited good cyclability over 250 cycles at 0.2C with a specific capacity of 500 mA h g−1.

One challenge associated with the utilization of block copolymers in nanotechnology is the difficulties associated with alignment and orientation of the self-assembled nanostructure on macroscopic length scales. Here we demonstrate a simple method to generate unidirectional alignment of the cylindrical domains of polystyrene-block-polyisoprene-block-polystyrene, SIS, based on a modification of the commonly utilized solvent vapor annealing (SVA) process. In this modification, cross-linked poly(dimethylsiloxane) (PDMS) is physically adhered to the SIS film during SVA; differential swelling of the PDMS and SIS produces a shear force to align the ordered domains of SIS in the areas covered by PDMS. This method is termed solvent vapor annealing with soft shear (SVA-SS). The alignment direction can be readily controlled by the shape and placement of the PDMS with the alignment angle equal to the diagonal across the rectangular PDMS pad due to a propagating deswelling front from directional drying of the PDMS by a dry air stream. Herman’s (second order) orientational parameter, S, can quantify the quality of the alignment over large areas with S > 0.94 obtainable using SVA-SS.

Stretchable conductive hydrogels with simultaneous high mechanical strength/modulus, and ultrahigh, stable electrical conductivity are ideal for applications in soft robots, artificial skin, and bioelectronics, but to date, they are still very challenging to fabricate. Herein, sandwich‐structured hybrid hydrogels based on layers of aramid nanofibers (ANFs) reinforced polyvinyl alcohol (PVA) hydrogels and a layer of silver nanowires (AgNWs)/PVA are fabricated by electrospinning combined with vacuum‐assisted filtration. The hybrid ANF‐PVA hydrogels exhibit excellent mechanical properties with the tensile modulus of 10.7–15.4 MPa, tensile strength of 3.3–5.5 MPa, and fracture energy up to 5.7 kJ m−2, primarily attributed to the strong hydrogen bonding interactions between PVA and ANFs and in‐plane alignment of the fibrous structure. Rational design of heterogeneous structure endows the hydrogels with ultrahigh apparent electrical conductivity of 1.66 × 104 S m−1, among the highest electrical conductivities ever reported so far for conductive hydrogels. More importantly, this ultrahigh conductivity remains constant upon a broad range of applied strains from 0–90% and over 500 stretching cycles. Furthermore, the hydrogels exhibit excellent Joule heating and electromagnetic interference shielding performances due to the ultrahigh electrical conductivity. These mechanically strong, hybrid hydrogels with ultrahigh and strain‐invariant electrical conductivity represent great promises for many important applications such as flexible electronics.