An official website of the United States government
The friction and wear behavior of materials are not intrinsic properties, but extrinsic properties; in other words, they can drastically vary depending on test and environmental conditions. In ambient air, humidity is one such extrinsic parameter. This paper reviews the effects of humidity on macro- and nano-scale friction and wear of various types of materials. The materials included in this review are graphite and graphene, diamond-like carbon (DLC) films, ultrananocrystalline diamond (UNCD), transition metal dichalcogenides (TMDs), hexagonal boron nitride (h-BN), boric acid, silicon, silicon oxide, silicates, advanced ceramics, and metals. Details of underlying mechanisms governing friction and wear behaviors vary depending on materials and humidity; nonetheless, a comparison of various material cases revealed an overarching trend. Tribochemical reactions between the tribo-materials and the adsorbed water molecules play significant roles; such reactions can occur at defect sites in the case of two-dimensionally layered materials and carbon-based materials, or even on low energy surfaces in the case of metals and oxide materials. It is extremely important to consider the effects of adsorbed water layer thickness and structure for a full understanding of tribological properties of materials in ambient air.
more »
« less
Switchable Slippery Surfaces Controlled by a Humidity‐Induced Glass Transition of Polyelectrolyte‐Grafted Brushes
Abstract Polymer brushes have found extensive applications as nano‐scale surface coatings with responsive properties, particularly in achieving tunable friction in solvent environments. Here, a special property of hygroscopic polyelectrolyte‐grafted brushes, where the friction forces change by over two orders of magnitude within a narrow range in humidity is reported. Using mechanical measurements of nano‐scale modulus and water absorption coupled with friction and surface‐sensitive spectroscopy, this sharp change in friction is controlled by a humidity‐induced glass transition that abruptly shifts the mode of sliding is demonstrated. Contrary to expectations based on conventional thinking regarding brush lubrication, friction remains large and humidity‐independent below the glass transition even for systems that absorb as much as 30–40% water by volume. This results in an abrupt change in friction past the glass transition humidity. Tuning the chemistry of brushes and their humidity‐induced glass transition offers the tunability to control the on/off friction (or slipperiness) for nanoactuators, ratchets, and catheters, without the need for externally applied lubricating liquids.
more »
« less
- Award ID(s):
- 2208464
- PAR ID:
- 10505152
- Publisher / Repository:
- Wiley Blackwell (John Wiley & Sons)
- Date Published:
- Journal Name:
- Advanced Materials Interfaces
- Volume:
- 11
- Issue:
- 13
- ISSN:
- 2196-7350
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
More Like this
-
-
Abstract This work examines the effect of environmental humidity on rate-and-state friction behavior of nanoscale silica-silica nanoscale contacts in an atomic force microscope, particularly, its effect on frictional ageing and velocity-weakening vs. strengthening friction from 10 nm/s to 100 μm/s sliding velocities. At extremely low humidities ($$\ll 1\% RH$$ ), ageing is nearly absent for up to 100 s of nominally stationary contact, and friction is strongly velocity-strengthening. This is consistent with dry interfacial friction, where thermal excitations help overcome static friction at low sliding velocities. At higher humidity levels (10–40% RH), ageing becomes pronounced and is accompanied by much higher kinetic friction and velocity-weakening behavior. This is attributed to water-catalyzed interfacial Si–O-Si bond formation. At the highest humidities examined (> 40% RH), ageing subsides, kinetic friction drops to low levels, and friction is velocity-strengthening again. These responses are attributed to intercalated water separating the interfaces, which precludes interfacial bonding. The trends in velocity-dependent friction are reproduced and explained using a computational multi-bond model. Our model explicitly simulates bond formation and bond-breaking, and the passivation and reactivation of reaction sites across the interface during sliding, where the activation energies for interfacial chemical reactions are dependent on humidity. These results provide potential insights into nanoscale mechanisms that may contribute to the humidity dependence observed in prior macroscale rock friction studies. They also provide a possible microphysical foundation to understand the role of water in interfacial systems with water-catalyzed bonding reactions, and demonstrate a profound change in the interfacial physics near and above saturated humidity conditions.more » « less
-
Abstract Block copolymer brushes are of great interest due to their rich phase behavior and value‐added properties compared to homopolymer brushes. Traditional synthesis involves grafting‐to and grafting‐from methods. In this work, a recently developed “polymer‐single‐crystal‐assisted‐grafting‐to” method is applied for the preparation of block copolymer brushes on flat glass surfaces. Triblock copolymer poly(ethylene oxide)‐b‐poly(l‐lactide)‐b‐poly(3‐(triethoxysilyl)propyl methacrylate) (PEO‐b‐PLLA‐b‐PTESPMA) is synthesized with PLLA as the brush morphology‐directing component and PTESPMA as the anchoring block. PEO‐b‐PLLA block copolymer brushes are obtained by chemical grafting of the triblock copolymer single crystals onto a glass surface. The tethering point and overall brush pattern are determined by the single crystal morphology. The grafting density is calculated to be ≈0.36 nm−2from the atomic force microscopy results and is consistent with the theoretic calculation based on the PLLA crystalline lattice. This work provides a new strategy to synthesize well‐defined block copolymer brushes.more » « less
-
Accumulated dust on solar cover glass reduces transmittance, leading to decreased energy efficiency of photovoltaic (PV) modules. Hydrophobic coatings on solar cover glass have been shown to provide anti-soiling properties when exposed to a condensing environment (e.g. dew). The addition of hydrophilic features along the top edge of the hydrophobic coated glass enhances condensation rates and can be used to achieve self-cleaning of the surfaces. However, to date, relatively long times have been required to clean the surfaces. In this study, we developed a new design for hydrophilic features that reduce the time required to clean the surface in laboratory tests as measured by laser scanning microscopy, optical photographs and UV–vis spectroscopy. The dagger-shaped features improve self-cleaning performance by a combination of three factors: a silica nanoparticle (NP) hydrophilic coating which enhances condensation rate due to a low water contact angle (WCA) and nano-scale porosity; the stepwise transition from the low WCA silica NP region to the high WCA silanized hydrophobic region via a bare glass transition zone; and the pointed shape of the hydrophobic dagger features which further minimizes the barrier for transport of droplets from the condensing region to the high-mobility, hydrophobic, region of the surface. The hydrophilic silica nanoparticle-coated dagger features not only improve the self-cleaning efficiency of the hydrophobic surfaces but also increase the overall amount of water harvested. Such coating designs provide an effective approach to reducing maintenance costs as well as increasing the overall energy output of PV panels.more » « less
-
Abstract A constant angle of twist was applied to silica glass rods in order to produce a torsional shear strain and a reduction in torque representative of the stress state in the glass was measured as a function of time when rods were heat‐treated in air at temperatures, 550‐700°C, far below the glass transition temperature. The monotonic decrease of torque with time was explained by surface stress relaxation, which can be described by a relaxation of stress at the surface of glass which is promoted by water. The obtained surface stress relaxation diffusion coefficients were consistent with those obtained earlier from silica glass fiber bending under a similar water vapor pressure. The observed relaxation in torsion supports the mechanism of surface stress relaxation over the swelling‐based mechanism for applications including glass fiber strengthening.more » « less
