TY - CONF

T1 - Nanoscale interfacial interactions of graphene with polar and non-polar liquids

AU - Robinson, Benjamin

AU - Kay, Nicholas

AU - Kolosov, Oleg

PY - 2014

Y1 - 2014

N2 - Graphene’s nanomechanical behaviour in liquids, vital for its operation in rechargeable batteries, super-capacitors, and sensors, is still largely unexplored. Here we will discuss the results of recent studies investigating the nanomechanics of normal (adhesive and elastic) and tangential (friction) forces between a stationary, moving and ultrasonically excited nanoscale atomic force microscope (AFM) tip and exfoliated few layer graphene (FLG) on SiO2 substrate as a function of surrounding media – air, polar (water) and non-polar (dodecane) liquids.We find that while the friction coefficient is significantly reduced in liquids, and is always lower for FLG than SiO2, it is higher for graphene in non-polar dodecane than highly polar water. We also confirm that in ambient environment the water meniscus dominates high adhesion for both hydrophobic FLG and the more hydrophilic SiO2 surface. By using nanomechanical probing via ultrasonic force microscopy (UFM) we observed profound reduction of graphene rippling and increase of graphene-substrate contact area in liquid environment. Friction force dependence on ultrasonic modulation amplitude suggests that dodecane at the graphene interface produces a solid-like “cushion” of approximately 2 nm thickness, whereas in water immersion, the same dependence shows remarkable similarity with ambient environment, confirming the presence of water meniscus in air, and suggesting negligible thickness of a similar water “cushion” on graphene.

AB - Graphene’s nanomechanical behaviour in liquids, vital for its operation in rechargeable batteries, super-capacitors, and sensors, is still largely unexplored. Here we will discuss the results of recent studies investigating the nanomechanics of normal (adhesive and elastic) and tangential (friction) forces between a stationary, moving and ultrasonically excited nanoscale atomic force microscope (AFM) tip and exfoliated few layer graphene (FLG) on SiO2 substrate as a function of surrounding media – air, polar (water) and non-polar (dodecane) liquids.We find that while the friction coefficient is significantly reduced in liquids, and is always lower for FLG than SiO2, it is higher for graphene in non-polar dodecane than highly polar water. We also confirm that in ambient environment the water meniscus dominates high adhesion for both hydrophobic FLG and the more hydrophilic SiO2 surface. By using nanomechanical probing via ultrasonic force microscopy (UFM) we observed profound reduction of graphene rippling and increase of graphene-substrate contact area in liquid environment. Friction force dependence on ultrasonic modulation amplitude suggests that dodecane at the graphene interface produces a solid-like “cushion” of approximately 2 nm thickness, whereas in water immersion, the same dependence shows remarkable similarity with ambient environment, confirming the presence of water meniscus in air, and suggesting negligible thickness of a similar water “cushion” on graphene.

M3 - Abstract

T2 - EMRS 2014, Spring Meeting

Y2 - 26 May 2014 through 30 May 2014

ER -