Mechanically tunable organogels from highly charged polyoxometalate clusters loaded with fluorescent dyes

Abstract Inorganic nanowires-based organogel, a class of emerging organogel with convenient preparation, recyclability, and excellent mechanical properties, is in its infancy. Solidifying and functionalizing nanowires-based organogels by designing the gelator structure remains challenging. Here, we fabricate Ca 2 -P 2 W 16 and Ca 2 -P 2 W 15 M nanowires utilizing highly charged [Ca 2 P 2 W 16 O 60 ] 10 − and [Ca 2 P 2 W 15 MO 60 ] 14 − /13 − cluster units, respectively, which are then employed for preparing organogels. The mechanical performance and stability of prepared organogels are improved due to the enhanced interactions between nanowires and locked organic molecules. Compressive stress and tensile stress of Ca 2 -P 2 W 16 nanowires-based organogel reach 34.5 and 29.0 kPa, respectively. The critical gel concentration of Ca 2 -P 2 W 16 nanowires is as low as 0.28%. Single-molecule force spectroscopy confirms that the connections between cluster units and linkers can regulate the flexibility of nanowires. Furthermore, the incorporation of fluorophores into the organogels adds fluorescence properties. This work reveals the relationships between the microstructures of inorganic gelators and the properties of organogels, guiding the synthesis of high-performance and functional organogels.