Diamond is the hardest material on Earth. Nevertheless, polishing diamond is possible with a process that has remained unaltered for centuries and is still used for jewellery and coatings: the diamond is pressed against a rotating disc with embedded diamond grit. When polishing polycrystalline diamond, surface topographies become non-uniform because wear rates depend on crystal orientations. This anisotropy is not fully understood and impedes diamond's widespread use in applications that require planar polycrystalline films, ranging from cutting tools to confinement fusion. Here, we use molecular dynamics to show that polished diamond undergoes an sp(3)-sp(2) order-disorder transition resulting in an amorphous adlayer with a growth rate that strongly depends on surface orientation and sliding direction, in excellent correlation with experimental wear rates. This anisotropy originates in mechanically steered dissociation of individual crystal bonds. Similarly to other planarization processes, the diamond surface is chemically activated by mechanical means. Final removal of the amorphous interlayer proceeds either mechanically or through etching by ambient oxygen.

The tribological performance of hydrogenated diamond-like carbon (DLC) coatings is studied by molecular dynamics simulations employing a screened reactive bond-order potential that has been adjusted to reliably describe bond-breaking under shear. Two types of DLC films are grown by CH2 deposition on an amorphous substrate with 45 and 60 eV impact energy resulting in 45 and 30% H content as well as 50 and 30% sp(3) hybridization of the final films, respectively. By combining two equivalent realizations for both impact energies, a hydrogen-depleted and a hydrogen-rich tribo-contact is formed and studied for a realistic sliding speed of 20 m s(-1) and loads of 1 and 5 GPa. While the hydrogen-rich system shows a pronounced drop of the friction coefficient for both loads, the hydrogen-depleted system exhibits such kind of running-in for 1 GPa, only. Chemical passivation of the DLC/DLC interface explains this running-in behavior. Fluctuations in the friction coefficient occurring at the higher load can be traced back to a cold welding of the DLC/DLC tribo-surfaces, leading to the formation of a transfer film (transferred from one DLC partner to the other) and the establishment of a new tribo-interface with a low friction coefficient. The presence of a hexadecane lubricant leads to low friction coefficients without any running-in for low loads. At 10 GPa load, the lubricant starts to degenerate resulting in enhanced friction

Amorphous hydrocarbon (a-C : H) films have enormous potential as low friction, wear resistant coatings. Here, we present a plasma assisted chemical vapour deposition process for a-C : H that exhibits growth rates of 100 nm min -1 and higher. The tribological performance of the resulting a-C : H films has been studied experimentally by reciprocating sliding of an a-C : H-coated Si 3 N 4 ball on an a-C : Hcoated 100Cr6 steel substrate and by subsequent micro Raman spectroscopy of the wear track. Running-in of the coatings is observed and characterised by a rapid decrease in the friction coefficient accompanied by a significant increase in sp 2 hybridisation in the wear track. In order to gain a deeper understanding of the underlying running-in mechanisms, the sliding of two a-C : H films under a load of 5 GPa has been studied by classical molecular dynamics employing a range-corrected Brenner bond-order potential. The simulations reproduce the experimental trends and explain the running-in by a combination of smoothing and chemical passivation of both tribosurfaces. Consequently, both mechanisms should be controlled in order to produce tribological coatings for applications with optimum energy-efficiency.

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