Illuminating Pathways to Dynamic Nanotribology: Light-Mediated Active Control of Interfacial Friction with Nanosuspensions.

Active control of nanotribological properties is a challenge. Materials responsive to external stimuli may catalyze this paradigm shift. Recently, the nanofriction of a thin film is modulated by light, ushering in phototribology. This frontier is expanded here, by investigating photoactive nanoparticles in lubricants to confer similar functionality to passive surfaces. Quartz-crystal microbalance (QCM) is employed to assess the phototribological behavior of aqueous suspensions of titanium dioxide nanoparticles. A comparison of dark and illuminated conditions provides the first demonstration of tuning the interfacial friction in solid-nanosuspension interfaces by light. Cyclic tests reveal reversible transitions between higher (dark) and lower friction (illuminated) regimes. These transitions are underpinned by transient states with surface charge variations, as confirmed by Zeta potential measurements. The accumulated surface charge increases repulsion within the system and favors sliding. Upon cessation of illumination, the system returns to its prior equilibrium state. These findings impact not only nanotribology but nanofluidics and nanorheology. Furthermore, the results underscore the need to consider light-induced effects in other scenarios, including the calculation of activity coefficients of photoactive suspensions. This multifaceted study introduces a new dimension to in operando frictional tuning, beckoning a myriad of applications and fundamental insights at the nanoscale.

Dynamics of Neutral and Charged Nanodiamonds in Aqueous Media Confined between Gold Surfaces under Normal and Shear Loading.

The dynamics of cubo-octahedral nanodiamonds (NDs) with three different surface treatments and confined in aqueous environments between gold surfaces under shear and normal loading conditions have been characterized via molecular dynamics (MD) simulations. The treatments consisted of carboxyl (-COO-) or amino (-NH3 +) groups attached to the NDs, producing either negatively or positively charged NDs, respectively, and hydrogen-terminated surfaces producing neutral NDs. Simulations were performed in the presence and absence of induced image charges to explore the impact of electrostatic interactions on friction and surface deformation. Significant deformation of the gold surfaces was observed for negatively charged NDs placed between gold surfaces under external loads that were sufficient to displace water from the contact. Rolling and relatively high friction levels were also observed for the negatively charged NDs under the same conditions. In contrast, the neutral and positively charged NDs exhibited sliding behavior with only minor deformation of the gold surfaces. The results suggest that the size of the surface functional group plays a major role in determining whether NDs slide or roll on solid contacts. Higher friction levels were also observed in conjunction with induced image charges in the gold contacts. The results demonstrate how surface functionalization and surface-induced charges can work in combination to profoundly influence tribological performance.

Interdependent Roles of Electrostatics and Surface Functionalization on the Adhesion Strengths of Nanodiamonds to Gold in Aqueous Environments Revealed by Molecular Dynamics Simulations.

Molecular dynamics simulations demonstrate that adhesion strengths as a function of charge for aqueous nanodiamonds (NDs) interacting with a gold substrate result from an interdependence of electrostatics and surface functionalization. The simulations reveal a water layer containing Na+ counterions between a negative ND with surface -COO- functional groups that is not present for a positively charged ND with -NH3+ functional groups. The closer proximity of the positive ND to the gold surface and the lack of cancelation of electrostatic interactions due to counterions and the water layer lead to an electrostatic adhesion force for the positive ND that is nearly three times larger than that of the negative ND. Prior interpretations of experimental tribological studies of ND-gold systems suggested that electrostatics or surface functionalization could be responsible for observed adhesion strength differences. The present work demonstrates how these two effects work together in determining adhesion for this system.

A comparative study of the nanoscale and macroscale tribological attributes of alumina and stainless steel surfaces immersed in aqueous suspensions of positively or negatively charged nanodiamonds.

This article reports a comparative study of the nanoscale and macroscale tribological attributes of alumina and stainless steel surfaces immersed in aqueous suspensions of positively (hydroxylated) or negatively (carboxylated) charged nanodiamonds (ND). Immersion in -ND suspensions resulted in a decrease in the macroscopic friction coefficients to values in the range 0.05-0.1 for both stainless steel and alumina, while +ND suspensions yielded an increase in friction for stainless steel contacts but little to no increase for alumina contacts. Quartz crystal microbalance (QCM), atomic force microscopy (AFM) and scanning electron microscopy (SEM) measurements were employed to assess nanoparticle uptake, surface polishing, and resistance to solid-liquid interfacial shear motion. The QCM studies revealed abrupt changes to the surfaces of both alumina and stainless steel upon injection of -ND into the surrounding water environment that are consistent with strong attachment of NDs and/or chemical changes to the surfaces. AFM images of the surfaces indicated slight increases in the surface roughness upon an exposure to both +ND and -ND suspensions. A suggested mechanism for these observations is that carboxylated -NDs from aqueous suspensions are forming robust lubricious deposits on stainless and alumina surfaces that enable gliding of the surfaces through the -ND suspensions with relatively low resistance to shear. In contrast, +ND suspensions are failing to improve tribological performance for either of the surfaces and may have abraded existing protective boundary layers in the case of stainless steel contacts. This study therefore reveals atomic scale details associated with systems that exhibit starkly different macroscale tribological properties, enabling future efforts to predict and design complex lubricant interfaces.

Quartz crystal microbalance apparatus for study of viscous liquids at high temperatures.

A design for a Quartz Crystal Microbalance (QCM) setup for use with viscous liquids at temperatures of up to 300 °C is reported. The system response for iron and gold coated QCM crystals to two common lubricant base oils, polyalphaolefin and halocarbon, is reported, yielding results that are consistent with theoretical predictions that incorporate electrode nanoscale surface roughness into their analysis.

Multiscale analysis of liquid lubrication trends from industrial machines to micro-electrical-mechanical systems.

An analytic multiscale expression is derived that yields conditions for effective liquid lubrication of oscillating contacts via surface flow over multiple time and length scales. The expression is a logistics function that depends on two quantities, the fraction of lubricant removed at each contact and a scaling parameter given by the logarithm of the ratio of the contact area to the product of the lubricant diffusion coefficient and the cycle time. For industrial machines the expression confirms the need for an oil mist. For magnetic disk drives, the expression predicts that existing lubricants are sufficient for next-generation data storage. For micro-electrical-mechanical systems, the expression predicts that a bound + mobile lubricant composed of tricresyl phosphate on an octadecyltrichlorosilane self-assembled monolayer will be effective only for temperatures greater than approximately 200 K and up to approximately MHz oscillation frequencies.