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This paper presents experimental investigations to actively modulate the nanoscale friction properties of a selfassembled monolayer (SAM) assembly using an external electric field that drives conformational changes in the SAM. Such "friction switches" have widespread implications in interfacial energy control in micro/ nanoscale devices. Friction response of a low-density mercaptocarboxylic acid SAM is evaluated using an atomic force microscope (AFM) in the presence of a DC bias applied between the sample and the AFM probe under a nitrogen (dry) environment. The low density allows reorientation of individual SAM molecules to accommodate the attractive force between the −COOH terminal group and a positively biased surface. This enables the surface to present a hydrophilic group or a hydrophobic backbone to the contacting AFM probe depending upon the direction of the field (bias). Synthesis and deposition of the low-density SAM (LD-SAM) is reported. Results from AFM experiments show an increased friction response (up to 300%) of the LD-SAM system in the presence of a positive bias compared to the friction response in the presence of a negative bias. The difference in the friction response is attributed to the change in the structural and crystalline order of the film in addition to the interfacial surface chemistry and composition presented upon application of the bias. Keywords Chemistry DisciplinesChemistry | Mechanical Engineering | Nanoscience and Nanotechnology CommentsReprinted with permission from Langmuir 25 (2009) This paper presents experimental investigations to actively modulate the nanoscale friction properties of a selfassembled monolayer (SAM) assembly using an external electric field that drives conformational changes in the SAM. Such "friction switches" have widespread implications in interfacial energy control in micro/nanoscale devices. Friction response of a low-density mercaptocarboxylic acid SAM is evaluated using an atomic force microscope (AFM) in the presence of a DC bias applied between the sample and the AFM probe under a nitrogen (dry) environment. The low density allows reorientation of individual SAM molecules to accommodate the attractive force between the -COOH terminal group and a positively biased surface. This enables the surface to present a hydrophilic group or a hydrophobic backbone to the contacting AFM probe depending upon the direction of the field (bias). Synthesis and deposition of the low-density SAM (LD-SAM) is reported. Results from AFM experiments show an increased friction response (up to 300%) of the LD-SAM system in the presence of a positive bias compared to the friction response in the presence of a negative bias. The difference in the friction response is attributed to the change in the structural and crystalline order of the film in addition to the interfacial surface chemistry and composition presented upon application of the bias.

In this study the friction and wear behavior of medical grade ultra-high molecular weight polyethylene (UHMWPE) (GUR 1050 resin) were evaluated as a function of polymer crystallinity. Crystallinity was controlled by heating UHMWPE samples to a temperature above its melting point and varying the hold time and cooling rates. Degree of crystallinity of the samples was evaluated using differential scanning calorimetry (DSC). Quantitative friction experiments were conducted at two different scales. A custom-made microtribometer with commercially available spherical Si3N4 probes in dry conditions was used to test friction at the microscale. An atomic force microscope with commercially available Si3N4 probes under dry conditions was used for nanoscale experiments. A higher degree of crystallinity in the UHMWPE resulted in lower friction force and an increase in scratch resistance at both scales. Reciprocating wear tests preformed using the tribometer show that higher crystallinity also results in lower friction, as well as lower wear depth and width.

Medical-grade UHMWPE samples with two different surface finishing treatments, milling and melting/reforming were exposed to 10% bovine serum albumin solution and their friction responses were quantified using atomic force microscopy. The observed friction increase upon exposure to proteins was attributed to the formation of a layer of denatured proteins on the surface. Changing the crystallinity and surface energy of UHMWPE affected the protein adsorption mechanism and the resulting increase in friction behavior.

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In this study, the friction and wear behavior of ultrahigh molecular weight polyethylene (UHMWPE) were evaluated as a function of polymer crystallinity in the presence of the phospholipid dipalmitoyl phosphatidylcholine (DPPC) dissolved in ethanol. Samples of UHMWPE were separately heat treated to get high and low crystallinity samples. Degree of crystallinity was evaluated using differential scanning calorimetry. Quantitative friction and wear experiments were conducted using a custom-made microtribometer with commercially available spherical Si(3)N(4) probes in controlled and phospholipid-dissolved lubricants. The higher crystallinity sample exhibited slightly lower friction than the lower crystallinity in the control and decreased significantly when phospholipids were present. The higher crystallinity sample showed a higher wear resistance than the lower crystallinity sample during all reciprocating wear tests. DPPC acting as a lubricant had a marginal effect on the wear resistance of high crystallinity UHMWPE, whereas the low crystallinity sample became more prone to wear. Atomic force microscopy topography images and contact angle measurements of both samples before and after phospholipid exposure indicate that the higher crystallinity sample absorbed a greater density of DPPC. Increasing crystallinity is a way of escalating adsorption of surface active phospholipids onto UHMWPE to make it a more wear-resistant load-bearing material for total joint replacements.

Tribological properties of materials used in biomedical implants critically affect the performance of the implant. A UHMWPE cup paired with a ceramic ball is a popular combination for implants due to its relatively low wear rate. In this study we investigate the effect of surface roughness of UHMWPE on the friction behavior and onset of wear in a UHMWPE/silicon nitride interface in both dry air and bovine serum environments. Microscale multi-asperity contact is examined using a ball-on-flat reciprocating microtribometer. Nanoscale single-asperity contact and surface topography are examined using atomic force microscopy. Friction was found to increase with a decrease in surface roughness of the UHMWPE sample in air, which is due to an increase in real area of contact. This trend was seen to disappear or even reverse in serum. This is due to an increase in the interfacial shear stress of the UHMWPE surface when exposed to the serum. This increase is believed to be caused by an adhered layer of protein on the UHMWPE surface.

The friction behavior of two different materials, mica and ultra-high molecular weight polyethylene (UHMWPE), was evaluated at the nanoscale with an atomic force microscope and with a custom-built ball-on-flat microtribometer at the microscale. The same counterface (Si 3 N 4 probe), environmental conditions (25°C, RH \ 10%), and similar load ranges were maintained for all experiments. The friction-force data obtained were analyzed for contact-area dependence. Friction force between silicon nitride and mica at the nanoscale showed initial non-linearity with normal load up to a certain load, beyond which surface damage was observed resulting in a linear dependence of friction force on normal load. At the microscale, the friction force of the mica-silicon nitride interface exhibited linear dependence on normal load. Friction force between silicon nitride and UHMWPE exhibited non-linearity with normal load at both the length scales, for the applied load ranges of our experiment. An appropriate contact mechanics theory was applied to calculate an interfacial shear strength value for the material pair at both the scales. The values at both the scales were similar, when the conditions were carefully maintained to be the same across scales.