the spectrum, thermoplastics can deform and flow when heated above their melting temperature but remain rigid at room temperature. Thermoplastic elastomers (TPEs) that combine the processability of thermoplastics and the elasticity of elastomers are attractive as tough yet stretchable and reprocessible materials. [2] Nevertheless, many TPEs are not repairable and often require elaborate synthesis.Stretchability, self-healing, and reprocessability could be achieved together through the introduction of non-covalent interactions or dynamic covalent bonds (DCBs). The former involves hydrogen bonding, [3] Coulombic interactions, [4] chain entanglement, [5] and supramolecular interactions, [6] which feature weak bond energies (compared to covalent bonds), as well as long healing times, slow stress relaxations, and a dependence on external stimuli. [7] DCBs, on the other hand, offer structural stability yet can undergo debonding and rebonding when activated. Therefore, DCBs are attractive for self-healing and reusability. [8] Commonly studied DCBs include ester, [9] disulfide, [10] imine, [11] thiol-X, [12] boronic ester, [13] and silyl ether bond. [14] Most DCBs, however, require high temperatures, the use of catalysts, or external stimuli to achieve reversible bonding and debonding. [8] Among them, boronic esters are readily reversible at room temperature without any catalyst or external stimuli. [8] Previous efforts primarily employed hydrophobic boronic acid (phenyl boronic acid, PBA) and catechol groups as the dynamic covalent crosslinker, resulting in elongations at break varying from 1.1 to 10 times of its original length, l o . [2,15] Replacing PBA with boric acid (BA) allows hydrogels to achieve similar stretchability (λ = l/l o , ≈7.5) and instant self-healing (within a few seconds) in the presence of alginates. [16] Alternatively, double networks (DNs) of two physically entangled matrices have shown promise to address the brittleness of conventional single network hydrogels. A typical double network includes a flexible but weak network A with loosely crosslinked covalent or non-covalent interactions, and a brittle but strong network B with permanently crosslinked covalent bonds. [17] The resulting DNs exhibit high toughness (fracture energy up to 9000 J m −2 ) and good stretchability (10 to 20). [4,7a,18] However, DNs are typically not reprocessible.Here, we integrate both designs into a DN hydrogel with DCBs. Poly(vinyl alcohol) (PVA) is crosslinked by BA through the formation of boronic ester, a type of DCB, referred as AB hydrogel, while chitosan forms the second network through Cell engineering, soft robotics, and wearable electronics often desire soft materials that are easy to deform, self-heal readily, and can relax stress rapidly. Hydrogels, a type of hydrophilic networks, are such kind of materials that can be made responsive to environmental stimuli. However, conventional hydrogels often suffer from poor stretchability and repairability. Here, hydrogels consisting of boronic ester dynamic covale...