Nonvolatile ionogels are promising soft electrolyte materials for flexible electronics, but it is challenging to fabricate stable electrolytes with mechanical robustness. Here, through rationally optimizing the chemical structure of polymer matrix and ionic liquids, the high-performance ionogel electrolytes with mechanical robustness and stability were fabricated. There are double hydrogen bonding networks in the as-prepared ionogel electrolytes, one of which exists between the polymer chains while the other one existing between the polymer chains and ionic liquid molecules. By adjusting the content of the ionic liquid and the ratio of the two hydrogen bonding networks, the prepared ionogel electrolytes exhibit tunable properties with an elasticity of 1.3–30 kPa, a stretchability of more than 1800%, a fracture energy of 125.8–548.3 KJ m–3, and a coordinated self-healing efficiency of 6.2–37.9% to satisfy the needs of different application scenarios. The assembled wearable sensors based on the high-performance ionogel electrolytes can be attached to a part of the human body, detecting various motions and body temperature. Benefiting from the nonvolatile and hydrophobic properties of the ionogel electrolytes, the wearable sensors can be operated under extreme environments including high/low temperature (−15–100 °C) and high humidity (100% relative humidity). It is believed that this work provides prospects for the application of wearable electronic devices.
To reach global carbon neutralization, the use of clean energy and biomaterials has become a trend to reduce CO 2 emission. With the increasing concerns about freshwater shortage and crude oil pollution, water purification and sewage treatment have become particularly urgent. Solar energy is an environment-friendly energy to mitigate freshwater shortage stress and reduce crude oil pollution. However, how to make solar energy applied to effectively drive freshwater generation and crude oil pollution remedy is crucial. Herein, the electrospun membrane was explored as sustainable matrix with desirable solar-to-thermal performance. The strategy of spectrum-tailoring was proposed to tailor bandgap energy of vanadium disulfide (VS 2 ) for photothermal conversion promotion and interfacial evaporation efficiency. Inspired by mussel, dopamine was polymerized on surface of VS 2 (VS 2 @PDA) for spectrum tailoring (Solar absorptance, α, is 89.34 %). Bandgap energy of the complex favorably decreased from 2.06 to 1.41 eV. Combining the dual H-bonding networks, water evaporation enthalpy of the membranes dramatically decreased from 2370 to 1990.2 J/g and the resulted evaporators showed excellent salt resistance, with evaporation rate of 1.40 kg m -2 h −1 (enhancement factor is 2.032) and extraordinary cyclic evaporation performance. Additionally, sunflower-inspired tilting model was architectured to eliminate disturbance of sun irradiation incident angles for effective solar-driven interfacial generation. The resulted membrane effectively treated the seawater and decreased high viscosity of the super-viscous crude oil under the sun irradiation, thus showing great potential in seawater treatment and crude oil pollution remedy. The designs maximized utilization of solar energy and evaporation rates by treating seawater and reducing crude oil pollution without consuming additional energy, thus contributing to carbon neutralization. Therefore, the integration of dual H-bonding networks and spectrum-tailoring strategies would facilitate the structure-functional unification and desirable photothermal capabilities, and bring about an application potential in the development of composite evaporators for carbon neutralization.
危险品化学品经营许可证（带存储）