These gels represent a class of soft materials with unique properties resembling soft biological tissues, such as tendons, ligaments, cartilage, muscles, and skin. [6] Hydrogels, obtained by cross-linking hydrophilic polymer chains in aqueous solutions, [7] possess the intrinsic lowmodulus nature and tissue-like properties, which make them applicable to tissue engineering, [8] optical devices, [9] biomedicine [10] and actuators. [11] In the pursuit of high performance, most research in the field of polymer gels has been focused on the chemical nature and polymer network architectures and their interactions, [12] such as ideal polymer networks, [13] interpenetrating polymer networks, [14] nano/micro composite polymer networks, [10,15] and hierarchically structured polymer networks. [16] The small molecule solvent is the second component of gels and is often considered to be a nonfunctional liquid that impregnates and expands a functional polymer network. Recently, ionic liquids have been used to replace water in hydrogels, [17] resulting in soft materials with long-term stability. [18] Multicomponent solvent systems, in which water is mixed with organic solvents (such as glycerol, [19] ethylene glycol [20] and sorbitol [21] ), were introduced into gel networks to maintain the performance of materials in harsh environments. However, because of the low molecular weight of solvents used and weak interactions with polymer networks, the reported Polymer gels, such as hydrogels, have been widely used in biomedical applications, flexible electronics, and soft machines. Polymer network design and its contribution to the performance of gels has been extensively studied. In this study, the critical influence of the solvent nature on the mechanical properties and performance of soft polymer gels is demonstrated. A polymer gel platform based on poly(ethylene glycol) (PEG) as solvent is reported (PEGgel). Compared to the corresponding hydrogel or ethylene glycol gel, the PEGgel with physically cross-linked poly(hydroxyethyl methacrylate-co-acrylic acid) demonstrates high stretchability and toughness, rapid self-healing, and long-term stability. Depending on the molecular weight and fraction of PEG, the tensile strength of the PEGgels varies from 0.22 to 41.3 MPa, fracture strain from 12% to 4336%, modulus from 0.08 to 352 MPa, and toughness from 2.89 to 56.23 MJ m -3 . Finally, rapid self-healing of the PEGgel is demonstrated and a self-healing pneumatic actuator is fabricated by 3D-printing. The enhanced mechanical properties of the PEGgel system may be extended to other polymer networks (both chemically and physically cross-linked). Such a simple 3D-printable, self-healing, and tough soft material holds promise for broad applications in wearable electronics, soft actuators and robotics.

Herein, we report the design of styrene-based poly(ethylene oxide) (PEO) side-chain block copolymers featuring a microphase separation and their application as solid polymer electrolytes in high-voltage lithium-metal batteries. A straightforward synthesis was established, overcoming typical drawbacks of PEO block copolymers prepared by anionic polymerization or ester-based PEO side-chain copolymers. Both the PEO side-chain length and the LiTFSI content were varied, and the underlying relationships were elucidated in view of polymer compositions with high ionic conductivity. Subsequently, a selected composition was subjected to further analyses, including phase-separated morphology, providing not only excellent self-standing films with intrinsic mechanical stability but also the ability to suppress lithium dendrite growth as well as good flexibility, wettability, and good contacts with the electrodes. Furthermore, good thermal and electrochemical stability was demonstrated. To do so, linear sweep and cyclic voltammetry, lithium plating/stripping tests, and galvanostatic overcharging using high-voltage cathodes were conducted, demonstrating stable lithium-metal interfaces and a high oxidative stability of around 4.75 V. Consequently, cycling of Li||NMC622 cells did not exhibit commonly observed rapid cell failure or voltage noise associated with PEO-based electrolytes in Li||NMC622 cells, attributed to the high mechanical stability. A comprehensive view is provided, highlighting that the combination of PEO and high-voltage cathodes is not impossible per se.

Potassium-ion batteries are an emerging post-lithium technology that are considered ecologically and economically benign in terms of raw materials' abundance and cost. Conventional cell configurations employ flammable liquid electrolytes that impose safety concerns, as well as considerable degrees of irreversible side reactions at the reactive electrode interfaces (especially against potassium metal), resulting in a rapid capacity fade. While being inherently safer, solid polymer electrolytes may present a solution to capacity losses owing to their broad electrochemical stability window. Herein, we present for the first time a stable solid-state potassium battery composed of a potassium metal negative electrode, a Prussian blue analogue K 2 Fe[Fe(CN) 6 ] positive electrode, and a poly(ethylene oxide)-potassium bis(trifluoromethanesulfonyl)imide polymer electrolyte. At an elevated operating temperature of 55 °C, the solid-state battery achieved a superior capacity retention of 90% over 50 cycles in direct comparison to a conventional carbonatebased liquid electrolyte operated at ambient temperature with a capacity retention of only 66% over the same cycle number interval.

No abstract

The inverse vulcanization produces high sulfur content polymers from alkenes and elemental sulfur. Control over properties such as the molar mass or the solubility of polymers is not well established, and existing strategies lack predictability or require large variations of the composition. Systematic design principles are sought to allow for a targeted design of materials. Herein, we report on the inverse vulcanization of norbornenylsilanes (NBS), with a different number of hydrolysable groups at the silicon atom. Inverse vulcanization of mixtures of NBS followed by polycondensation yielded soluble high sulfur content copolymers (50 wt % S) with controllable weight average molar mass (M W ), polydispersity (Đ), glass transition temperature (T G ), or zero-shear viscosity (η 0 ). Polycondensation was conducted in the melt with HCl as a catalyst, abolishing the need for a solvent. Purification by precipitation afforded polymers with a greatly reduced amount of low molar mass species.