Shear of confined perfluorinated molecules: Effect of side branching

Abstract

To understand the dependence of nanorheology on molecular architecture for perfluorinated molecules, studies were performed using two lubricants commonly used in the magnetic storage industry. Experiments mimicked a single asperity by confining liquids to molecular spacings between atomically smooth mica and applying oscillatory shear forces. The force-distance profiles were compared. Large differences were obtained for the linear shear response. The elastic and dissipative shear moduli of a branched perfluoropolymer (Krytox-AZ) were comparable even at high loads, signifying that the fluid remained fluid-like over experimental frequencies. However, linear perfluoropolymer (Demmim S-20) was easily solidified. The nonlinear responses were also surprising. Previously, we (G. Reiter et al., Science 263 (1994) 1741) reported that the shear-induced transition from an elastic state (at rest) to a dissipative state (during sliding) was discontinuous and hysteric for various hydrocarbon fluids but not for the perfluorinated chain, perfluoroheptaglyme. However, the stick-slip transition was discontinuous, and even more hysteretic for the linear perfluoropolymer (Demnum S-20).