Dynamic Covalent Oleogel with Mechanical Force-Induced Reversible Phase Transition for Self-Adaptive Lubrication

Substantial progress has been made in stimulus-responsive and performance-tunable hydrogels, yet endowing organogels with dynamic adaptive properties remains challenging. Especially, the development of adaptive functional oleogel materials is further constrained by weak interactions between the oil and the gel network, along with the high viscosity ofoil. Herein, the state self-adaptability ofoleogels is enabled by constructing mechanical responsive dynamic covalent networks via ring-opening polymerization ofthioctic acid (TA). Mechanically responsive breaking and rebuilding ofdisulfide bonds endow mechanical force-induced reversible phase transition ofpoly(TA) oleogels. Mechanical force-induced disulfide bond breakage disrupts the gel network, transforming the gel into a sol state. Once the mechanical force is removed, the rapid bonding ofsulfur radicals rebuilds the gel network. Furthermore, this highly generalizable strategy has the potential as a self-adaptive lubricant. Self-adaptive oleogels can exist in a gel or sol state that adapts to whether the machine is running or stopped. Systematic tribological tests confirm the excellent lubricating properties of poly(TA) oleogels and their outstanding performance stability in adapting to changing friction conditions. This adaptive poly(TA) oleogels provides insights for developing oleogel functional materials with dynamic properties, as well as a new strategy for the development ofsmart lubricating materials.