The role of hydrogen on the friction mechanism of diamond-like carbon films

Abstract

The structure, properties and tribological behavior of DLC films are dependent on the deposition process, the hydrogen concentration and chemical bondings in the films. The present paper reports selected tribological experiments on model DLC films with different hydrogen contents. The experiments were performed in ultrahigh vacuum or in an atmosphere of pure hydrogen or argon in order to elucidate various friction mechanisms. Two typical friction regimes are identified. High steady-state friction in UHV (friction coefficient of 0.6) is observed for the lowest hydrogenated and mostly sp²-bonded DLC film. Superlow steady-state friction (friction coefficient in the millirange) is observed both for the highest hydrogenated film in UHV, and for the lowest hydrogenated film in an atmosphere of hydrogen (10 hPa). The high steady-state friction in UHV, observed for the lowest hydrogenated film with a dominant sp² carbon hybridization, is associated with a π–π^* sub-band overlap responsible for an increased across-the-plane chemical bonding with a high shear strength similar to what is observed with unintercalated graphite in the same UHV conditions. Superlow friction is correlated with a hydrogen saturation across the shearing plane through weak van der Waals interactions between the polymer-like hydrocarbon top layers. This regime is observed during the steady-state period if the film contains enough hydrogen incorporated during deposition. If this condition is not satisfied (i.e., for the film with the lowest hydrogen content), the limited diffusion of hydrogen from the film network towards the sliding surfaces seems to be responsible for a superlow running-in period. The superlow friction level can be reached over longer time periods by suitable combinations of temperature and molecular hydrogen present in the surrounding atmosphere during friction.