Abstract

The understanding of friction on soft sliding biological surfaces at the nanoscale is poorly understood as hard interfaces are frequently used as model systems. Herein, we studied the influence of elastic modulus on the frictional properties of model surfaces at the nanoscale for the first time. We prepared model silicone-based elastomer surfaces with tuneable modulus ranging from hundreds of kPa to a few MPa, similar to those found in real biological surfaces, and employed atomic force microscopy to characterize their modulus, adhesion, and surface morphology. Consequently, we used friction force microscopy to investigate nanoscale friction in hard-soft and soft-soft contacts using spherical colloidal probes covered by adsorbed protein films. Unprecedented results from this study reveal that modulus of a surface can have a significant impact on the frictional properties of protein-coated surfaces with higher deformability leading to lower contact pressure and, consequently, decreased friction. These important results pave the way forward for designing new functional surfaces for serving as models of appropriate deformability to replicate the mechanical properties of the biological structures and processes for accurate friction measurements at nanoscale.

Highlights

  • A plethora of soft sliding interfaces exist in the human body as well as in technological applications where low friction is often a requirement to ensure proper functioning

  • We utilised friction force microscopy to study the impact of elastic modulus on the frictional properties of soft surfaces coated with protein films at the nanoscale

  • We built model silicone-based elastomer surfaces with tuneable elasticity that can be used as model systems in the nanoscale to replicate biointerfaces such as those found in the oral cavity or the synovial joints

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Summary

Introduction

A plethora of soft sliding interfaces exist in the human body as well as in technological applications where low friction is often a requirement to ensure proper functioning. The differences in frictional properties in hard–hard versus hard–soft or soft–soft contacts could arise due to deformation and adhesion forces changing the contact area, smoothing surface nanometric roughness, or due to molecular arrangement effects such as dissipation, entanglement or rapid adsorption/desorption Another factor that needs to be considered is that biological surfaces are often coated with a proteinaceous film that mediates friction and, the mechanical properties as well as the surface chemistry of the model surface can have a great impact in dictating the adhesion and friction of proteins on those surfaces. We report a clear dependency of friction on the Young’s modulus of the substrate To date, this is the first study that sheds light on the impact of elasticity on the frictional properties of protein-coated soft surfaces, which is anticipated to have an impact on designing new functional model surfaces for studying soft–soft contact friction in nanoscale for various biophysical and technological applications

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