“…Luminescent metallo-supramolecular polymers derived from the coordination between ditopic ligands and lanthanide ions (Ln 3+ ) have been reported to exhibit superior self-healing behavior. − Unfortunately, their mechanical strength is insufficient for processing into self-standing films, which hinders their practical implementation in self-healing light-converting films. − The combination of dense coordination bonds and hydrogen bonds (H-bonds) within the polymer chain can endow the final products with intriguing self-healing properties and satisfactory mechanical strength. − Transition metal ions such as Zn 2+ , Cu 2+ , and Fe 3+ are commonly employed to coordinate with ligands attached to polymer chains, forming robust self-healing polymers. − Motivated by this concept, our group recently reported luminescent polymers through the coordination bonds between Ln 3+ and polymer ligands containing terpyridine as well as H-bonds among the polymer chains. These polymers exhibit high luminescence characteristics typical of lanthanide complexes, resulting from energy transfer from ligands to Ln 3+ , and promising mechanical strength alongside remarkable self-healing abilities due to the reversibility of the coordination bonds and H-bonds within these systems. , Furthermore, stimulus-responsive luminescence has been simultaneously achieved in certain instances. , In addition, the luminescence, self-healing, mechanical properties, and stimulus-responsiveness of these polymers can be conveniently modulated by altering the ligand moieties capable of coordinating with Ln 3+ and the structure of the polymer chain to which the ligands are tethered. , However, most luminescent polymers tend to lose their exceptional mechanical properties under high humidity as polymers with polar groups can absorb water and become easily plasticized. − Moreover, the transmittance of such polymers significantly decreases due to the presence of absorbed water, impeding their application in optical and display devices .…”