Although earthquakes are one of the most notorious natural disasters, a full understanding of the underlying mechanisms is still lacking. Here, nanoscale friction measurements were performed by atomic force microscopy (AFM) on calcite single crystals with an oxidized silicon tip to investigate the influence of roughness, contact aging, and dry vs. aqueous environment. In dry environments, smooth and rough calcite surfaces yielding single- and multiasperity contacts, respectively, exhibit velocity-weakening ( β D ln V ) or neutral friction at slow sliding velocities and velocity-strengthening friction ( α D ln V ) at higher velocities, while the transition shifts to slower velocities with an increase in roughness. The origin of the velocity-weakening friction is determined to be contact aging resulting from atomic attrition of the crystalline surface. Friction measurements in aqueous environment show evidence of pressure solution at sufficiently slow sliding velocities, which not only significantly reduces friction on single-and multiasperity contacts but also, eliminates atomic attrition and thereby, velocity-weakening friction. Importantly, the friction scaling law evolves from logarithmic ( β D ln V ) into linear ( α P S V ), deviating from commonly accepted rate-and-state friction (RSF) laws; this behavior extends over a wider range of velocities with higher roughness. Above a transition velocity, the scaling law remains logarithmic ( α W ln V ). The friction rate parameters α D , β D , α P S , and α W decrease with load and depend on roughness in a nonmonotonic fashion, like the adhesion, suggesting the relevance of the contact area. The results also reveal that parameters and memory distance differ in dry and aqueous environments, with implications for the understanding of mechanisms underlying RSF laws and fault stability.
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The Effects of Humidity on the Velocity-Dependence and Frictional Ageing of Nanoscale Silica Contacts
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.
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- Award ID(s):
- 1951314
- PAR ID:
- 10534329
- Publisher / Repository:
- Springer Science + Business Media
- Date Published:
- Journal Name:
- Tribology Letters
- Volume:
- 72
- Issue:
- 4
- ISSN:
- 1023-8883
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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