structures to enhance the van der Waals interactions with the substrate. [5-7] Reversible and stimuli-responsive adhesives can also be fabricated based on stimuliresponsive polymers or polymer systems involving reversible and dynamic molecular interactions, such as the introduction of temperature or light isomerization groups, [8-10] dynamic covalent bonds [11,12] (e.g., Diels-Alder reaction, disulfide bonds) and reversible noncovalent interactions [13-20] (e.g., hydrogen bonds, metal-ligand and host-gust interactions). However, these adhesives were mostly reported to exhibit high-performance bonding with high-surface-energy substrates, such as glass and metal. The adhesion of inert low-surface-energy substrates, typically exampled by polytetrafluoretyhylene (PTFE), has been a long-standing challenge, because such substrates resist wetting and possess limited functional groups to form interfacial interactions with the adhesives. [21] Therefore, it is still highly desirable to develop substrate-independent, reversible and easyrelease temporal adhesives with high bonding strength. For the temporal adhesives that bond substrates based on their intrinsic viscoelastic properties, the bonding performance depends on both the adhesive and cohesive strength. [22-28] The adhesive strength is determined by the wetting ability of the adhesive and the interfacial interactions between the adhesive and substrates, whereas the cohesive strength depends on the mechanical rigidity of the adhesive. [26-28] Therefore, the adhesive with higher cohesive strength should be more solid-like with lower deformability, which, however, would prevent the wetting of the substrates by the adhesive and in turn may result in lower bonding performance. Conversely, the adhesives with higher adhesive strength should be more fluid-like with higher deformability, which would result in lower cohesive strength and thus may lower the bonding performance as well. Therefore, it is a big challenge to optimize the viscoelastic properties of a temporal adhesive to balance the adhesive and cohesive strength to maximize the bonding performance. Herein, taking advantages of the good wetting ability and nonvolatility of ionic liquids (IL), [29-31] ionogel adhesives are prepared by blending an imidazolium-based IL with a copolymer bearing charged quaternary amine groups. Homogeneous and stable ionogels can be obtained due to the electrostatic interactions between the charged moieties of the IL and the copolymer. The IL can promote the continuous contact between the