“…The ability to remotely modulate ion and/or charge transport using light not only is essential for neurological activity in nature but also enables the fabrication of multifunctional smart materials including photoswitchable organic light-emitting transistors, supramolecular hydrogels, metal organic frameworks, and semiconductors . By introducing light-responsive functional groups into these materials, the optical and/or electrical properties can be noninvasively tuned with excellent spatial and temporal resolution, making them pivotal components for emerging optoelectronics applications such as smart displays, photodetectors, and logic circuits. ,− Among these materials, polymer electrolytes are an attractive platform due to their high ionic conductivity, tunable polymeric scaffold, and robust mechanical properties. , Importantly, ion mobility and conductivity in these materials are highly dependent on different types of weak interactions, such as cation–anion, polymer–ion, and Lewis acid–base interactions. , The rational and noninvasive modulation of these weak interactions by integrating light-responsive moieties into the structure of polymer electrolytes provides an elegant way to tune the ion mobility and conductivity in situ. , Huang and co-workers reported supramolecular ion-conducting hydrogels using azobenzene to mediate reversible changes in conductivity by competitive guest–host interactions. ,, We recently developed a photoswitchable polymeric ionic liquid based on imidazolium-containing diarylethene (DAE) cations and observed that ionic conductivity can be reversibly modulated by tuning the positive charge distribution and cation–anion interaction upon light irradiation . However, current light-responsive ion-conducting polymer electrolytes have relatively poor solid-like mechanical properties, because they are either viscous liquids with a low glass-transition temperature ( T g ≪ 20 °C) or solvent-containing hydrogels. , Consequently, the materials are difficult to integrate into devices. − The development of light-responsive, ion-conducting polymers that are mechanically robust, capable of self-healing, and inherently tunable remains a major challenge.…”