High–energy density lithium (Li) metal batteries (LMBs) are promising for energy storage applications but suffer from uncontrollable electrolyte degradation and the consequently formed unstable solid-electrolyte interphase (SEI). In this study, we designed self-assembled monolayers (SAMs) with high-density and long-range–ordered polar carboxyl groups linked to an aluminum oxide–coated separator to provide strong dipole moments, thus offering excess electrons to accelerate the degradation dynamics of carbon-fluorine bond cleavage in Li bis(trifluoromethanesulfonyl)imide. Hence, an SEI with enriched lithium fluoride (LiF) nanocrystals is generated, facilitating rapid Li + transfer and suppressing dendritic Li growth. In particular, the SAMs endow the full cells with substantially enhanced cyclability under high cathode loading, limited Li excess, and lean electrolyte conditions. As such, our work extends the long-established SAMs technology into a platform to control electrolyte degradation and SEI formation toward LMBs with ultralong life spans.

Traditional hydrogels always lose their flexibility and functions in dry environments because the internal water inevitably undergoes evaporation. In this study, a skin-inspired, facile, and versatile strategy for developing encapsulated hydrogels with excellent water retention capacity through a double-hydrophobic coating is proposed. The robust double-layer coating, which integrates a hydrophobic polymer coating with a hydrophobic oil layer simultaneously, can provide a barrier to prevent the evaporation of water. To overcome the weak interfacial strength between the hydrophilic hydrogel surface and the double-hydrophobic coating, (3-aminopropyl) triethoxysilane (APTES) is utilized as a chemical binding agent. Furthermore, the overall mechanical properties of the bulk hydrogel are not significantly affected, because the coating is only anchored to the surface and its thickness is much lower than that of the native hydrogel. Moreover, it is demonstrated that this proposed strategy particularly holds the capability of encapsulating various types and different shapes of hydrogels, leading to enhanced stability and a prolonged lifetime in air. Therefore, the proposed technology provides new insights for multifarious surface functionalization of hydrogel and broadens the range of hydrogel applications.

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Based on the host–guest interaction between anchored Noria and the amine monomer, high-performance nanofiltration membranes with nanostrand-hybrid morphology were fabricated.