Lubricants 2013, 1(2), 22-47; doi:10.3390/lubricants1020022

Nanotribological Behavior of Carbon Based Thin Films: Friction and Lubricity Mechanisms at the Nanoscale
Costas A. Charitidis *, Elias P. Koumoulos and Dimitrios A. Dragatogiannis
Department of Chemical Engineering 9 Heroon, National Technical University of Athens, Polytechneiou Street, Zografos, Athens GR-15780, Greece; E-Mails: (E.P.K.); (D.A.D.)
Author to whom correspondence should be addressed; E-Mail:; Tel.: +30-2107-724-046; Fax: +30-2107-722-339.
Received: 31 December 2012; in revised form: 28 January 2013 / Accepted: 1 March 2013 /
Published: 2 April 2013


: The use of materials with very attractive friction and wear properties has raised much attention in research and industrial sectors. A wide range of tribological applications, including rolling and sliding bearings, machining, mechanical seals, biomedical implants and microelectromechanical systems (MEMS), require thin films with high mechanical strength, chemical inertness, broad optical transparency, high refractive index, wide bandgap excellent thermal conductivity and extremely low thermal expansion. Carbon based thin films like diamond, diamond-like carbon, carbon nitride and cubic boron nitride known as “super-hard” material have been studied thoroughly as the ideal candidate for tribological applications. In this study, the results of experimental and simulation works on the nanotribological behavior of carbon films and fundamental mechanisms of friction and lubricity at the nano-scale are reviewed. The study is focused on the nanomechanical properties and analysis of the nanoscratching processes at low loads to obtain quantitative analysis, the comparison obtain quantitative analysis, the comparison of their elastic/plastic deformation response, and nanotribological behavior of the a-C, ta-C, a-C:H, CNx, and a-C:M films. For ta-C and a-C:M films new data are presented and discussed.
amorphous carbon films; nanocomposites; nanoindentation; friction; nanotribology; lubricity; wear; molecular dynamics

1. Introduction

1.1. Definition

Carbon-based thin films possess unique and adjustable combination of properties such as high hardness, wear resistance, chemical resistance and good tribological performances. Among critical variables to tailor carbon thin film’s properties for specific application are the distribution of the carbon hybridization states (sp1, sp2, sp3 bonds), the atomic H content, the content in dopants such as Si, F, N, B and O. Several types of carbon and carbon-based thin films are mentioned [1]:


a-C and hydrogenated amorphous carbon (a-C:H) films with a mixture of sp2 and sp3 bonding, highly sp3-boned material (ta-C) and sp2-bonded carbon


Carbon nitride (a-CNx)


Metal/Amorphous carbon (a-C:M) composite films

Nanotribological and nanomechanics studies are essential in order to develop fundamental understanding of interfacial phenomena on a small scale in micro/nanostructures used in magnetic storage systems, micro/nanoelectromechanical systems (MEMS/NEMS), and other applications. In nanomanufacturing technology, many small-scale devices cannot be miniaturized further, because friction and wear appear to be exceedingly large in nanoscale machines. Many drawbacks seems to arise because the surface-to-volume ratio is large in small systems and thus surface forces such as friction become relatively large. The friction force at the nano-scale increases with the applied normal load and the tip size because of the increase in the contact area [2]. The friction at the nano-scale is governed mainly by its adhesive characteristics, but the friction at the micro-scale is greatly affected by the wear behavior since the asperity contacts are predominantly plastic and deformation is an important factor [2]. The lower frictional property of diamond-like carbon (DLC) at the nano-scale compared to that of Si-wafer is attributed to the smaller contact area and the lower adhesive force, which are affected by the lower interfacial energy.

The coefficient of friction (CoF) represents, in principle, the friction between the structural material and diamond indenter probe. It is, in perspective, a dynamic rather than static, friction coefficient. In the contact-area-based approach, the CoF is decomposed into two components: shear (CoFS) and plowing (CoFP) [3,4]. The shear contribution is related to surface chemistry, whereas the plowing contribution is related to plastic deformation of the sample. Many theoretical studies and, most recently, an increasing number of experiments indicate that shear forces can be tremendously small between two atomically flat surfaces. These findings spur the hope for new avenues to reduce friction in nanoscale applications [5]. The last two decades, the frictional behavior of a single-asperity contact can be studied due to the introduction of new experimental tools (Atomic Force Microscopy, Lateral Force Microscopes), which made the nanometer and atomic scales accessible to tribologists [6,7,8,9,10]. It is the hope that once the atomic-scale manifestations of friction at such a nanometer-sized single asperity have been clarified, macroscopic friction could be explained with the help of statistics, i.e., by the summation of the interactions of a large number of small individual contacts, which form the macroscopic roughness of the contact interface [10]. A unified and clear understanding behind the mechanism of nano-scale friction is yet to be achieved. Given the importance of this topic, driven by the development of nanotechnology, the need for continued research effort in nano-tribology remains.

1.2. Scientific Fundamentals

When two solid bodies contact each other and one body begins to slide against the other, a frictional phenomenon appears. The friction force is defined as the drag against sliding, appearing along the contacting surfaces. According to the relative motion of two bodies, the friction forces are classified into static and dynamic ones, having different physical origins. The static friction force is characterized by the maximum force necessary to begin to slide one body against the other, whereas the dynamic friction force is the force applied to continue to slide one body against the other with a finite velocity (the energy must be dissipated during sliding). Experimentally, it is known that the dynamic friction force depends less on the sliding velocity.

Carbon-based thin films possess unique and adjustable combination of properties such as high hardness (H) and elastic modulus (E), wear resistance, chemical resistance and good tribological performances. Among critical variables to tailor a-C film’s properties for specific application are the distribution of the carbon hybridization states (sp1, sp2, sp3 bonds), the atomic H content, and the content in dopants such as Si, F, N, B and O.

Diamond related materials (i.e., carbon nitride and cubic boron nitride [c-BN]) are some of the harder materials known and provide advantageous properties (e.g., high mechanical strength, chemical inertness, and very attractive friction and wear properties). Most of these superhard materials provide optical transparency, enhanced refractive index and excellent thermal conductivity, to name a few. All the aforementioned qualities make diamond, DLC, and other related materials ideal candidate materials in the industrial field [1,11,12].

Carbon-based thin films have been developed to address a broad range of film applications, including one that demands outstanding tribological performance in a wide variety of operating environments. Carbon can adopt a large number of stable forms because of its ability to hybridize in multiple stable bonding states and to bond strongly with many other atoms. In addition to tailoring the hybridization state and the atomic H content, various dopants, such as Si, N, B, F, O, can be used to modify the surface energy, electrical, and mechanical properties. Amorphous carbon (a-C) is a disordered material with short range order, which is directly related to the optical and electric properties. The interatomic distances and interbonding angles can significantly deviate from those of the crystalline fully sp2-(sp3-) bonded graphite (diamond) lattice, since a-C contains mixtures of hybrid bonding states (sp1, sp2, sp3). Amorphous carbon (a-C) films possess a unique and adjustable combination of properties such as high hardness, wear resistance, chemical resistance and good tribological performances. They have low CoFs and provide protection for the counterparts [11,12,13,14,15,16].

Hydrogenated amorphous carbon (a-C: H), also called DLC (in literature some definitions of DLC can be found, i.e., a-C:H including sp3 bonds -even very few-, a-C:H which is predominantly sp3 bonded etc.), is an amorphous network composed of carbon and hydrogen. This network consists of strongly cross-linked carbon atoms with mainly sp2 (graphitic-like) and sp3 (diamond-like) bonds.

The properties of these films depend strongly on the hydrogen content and the sp3/sp2 ratio, which in turn, depend on the deposition process and its parameters. Another subclass of DLC, the tetrahedral amorphous carbon films (ta-C), are hydrogen free and the carbon atoms are mostly (>80%) carbon sp3 hybridized. The ta-C films are mainly produced from pure carbon targets by filtered vacuum arc or by pulsed laser deposition. Considerable research effort has been dedicated to the study of tribology, over many decades. This has been driven by the importance of mechanical devices in an array of modern era applications. A readily observable technological trend is toward miniaturization and there has been a lot of discussion about the possibility of producing mechanical devices with dimensions measured at the micro/nano-scale [17]. There has been a clear trend toward smaller electronic devices, which has driven the development of techniques for micro-fabricating Si and the production of MEMS (e.g., data recording head and accelerometer). Nevertheless, the further development of MEMS and particularly moving mechanical arrays (MMA) has been restricted due to the poor tribological properties of Si. It is essential for many MEMS components to have a low friction and low wear surface. Until recently, little work has been devoted to nanotribology and this is perhaps partially due to the lack of effective test methods that are relevant to the operational conditions of proposed MEMS devices, in which case loads of a few micro/milli-Newtons are typical at contact areas and moving distances of a few microns, contact pressures of tens to hundreds of MPa with wear depths limited to nm [18,19,20]. There is a limited relevance to the use of macro-scale testing for predicting nanoscale behavior [21]. Advances of microelectromechanical system technology in the past decade render the understanding of scale effects in tribology especially important, because surface to volume ratio grows with miniaturization and surface phenomena dominate. Microscale and nanoscale friction force measurements can be obtained with various instruments, such as friction force microscope, atomic force microscopy, and scratch test with apparatus able to make finely controlled low-load scratches (in the range of nN–μΝ) [22,23,24,25,26]. In Figure 1, the compositions of the various forms of amorphous C-H alloys on a ternary phase diagram with a hardness map are presented [11].

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Figure 1. Different compositions of common carbon-based materials in correspondence with hardness and coefficient of friction [1,11].

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Figure 1. Different compositions of common carbon-based materials in correspondence with hardness and coefficient of friction [1,11].
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In many studies, continuum mechanics appears to provide an accurate description of the nanometer-scale contact area and other contact properties of carbon based thin films. Homogeneity, isotropy, linearity, and elasticity of the materials are important parameters to consider (several modified continuum contact mechanical models describing other cases have been applied). On the other hand, the current experimental testing systems exhibit significant difficulties in providing results in nanoscale (at a few nm). The difficulties with experimental methods at very small depths can, in general, be easily resolved by using atomistic simulations to solve a variety of problems at the nano scale and to simulate experiments. Defining contact area is one of the major challenges for understanding friction in nanoscale contacts of carbon based structures. Widely in the literature, friction laws are established in nanoscale contacts by large-scale Molecular Dynamics (MD) simulations with realistic force fields (absence—or not—of van der Waals forces). Many challenges can be overcome by MD simulations in order to identify atomistic phenomena underlying friction. By understanding friction at the atomic level, it is possible to build a useful design strategy for the development of low-friction technology. For instance, as reported by MD simulations, adhesion between the probe and the carbon film increases the calculated friction, while tribochemical reactions within the film led to a restructuring of the film and a reduction in friction [27,28]. In addition, there is actually no standard that relates adhesion and friction, which means that range of expected reduction in friction per unit reduction of adhesion, is not known.

2. Discussion

2.1. Surface Chemistry

The low macroscopic friction of diamond in air (μ = 0.05–0.1) has been attributed to the passivation of the surface by –H and –OH groups and/or by the production of lubricious sp2-bonded species. Nanotribology studies put these ideas to the test, and a significant recent success has been the clear demonstration that –H termination reduces nanoscale friction dramatically [29]. Removal of the H from the surface causes an increase in the average CoF by more than two orders of magnitude compared with the H-terminated surface; dangling bonds can bridge an interface and increase the contribution of adhesion to friction, and passivation of those reactive bonds can reduce those forces in a dramatic way.

Comparing many other a-C:H thin films from Plasma Enhanced Chemical Vapor Deposition (PECVD), High-Density Plasma (HDP) and other Ultra High Vacuum (UHV) processes, a threshold (not constant) in hydrogen content can be evidenced for each process between superlow friction, at high hydrogen content, and high friction, at low hydrogen content, attributed to differences in the structure of the films, especially different amounts of hydrogen unbounded to carbon and the presence of aromatic clusters. Hydrogen amount on the surface has an effect on the interactions between contacting surfaces. In the film, it will have an effect on the cross-linking of the random network of carbon atoms. Increase of hydrogen content usually leads to more “polymer-like” structures, with high fraction of C-H sp3 bonds, but such tendency is also strongly dependent on deposition process. Adhesion results in loss of superlow friction, probably due to interactions between the π-orbitals of sp2 carbon atoms. Essentially, in order to achieve superlow friction, one has to control the composition of the sliding surfaces as well as the rheology of the transfer film [30]. Either the hydrogen content of the pristine a-C:H film is sufficient to avoid sp2 carbon interactions, providing also a viscoplastic character to the film which probably helps in transfer film growth, or one has to feed the a-C:H and transfer film surface with hydrogen to avoid adhesive interactions and to modify the interfacial material, in order to allow a “healing” effect on the damaged surfaces. Oxygen might act in a selective removal process of sp2 carbon atoms. However, at higher pressures of oxygen, the removal of the transfer film is almost complete, leading to CoF in the 0.2–0.3 range (role of the transfer film on friction reduction) [31].

The tribological behavior of carbon-based thin films is strongly affected by their chemical composition, polycrystalline structure and surface morphology [32]. In all environments, the tribological behavior of carbon thin films is controlled by an interfacial transfer layer formed during friction. The aforementioned layer is formed by a friction-induced modification of the top layer of the film into a material of low shear strength. Despite this comprehension at a macroscopic scale, very little is reported on the mechanisms that control friction at a nanoscopic level. In addition, it has been demonstrated that for graphite and hydrogenated carbon films the macro-tribological behavior is not directly comparable with the nanotribological one, due to dependence of wear, plastic deformation and delamination on the contact area [32]. For the case of a-CNx films, higher CoF is attributed to the fact that N atoms change the polycrystalline structure of the carbon films and thus the number of phonon modes available for excitation. The improved properties of the a-CNx films are attributed to a “fullerene-like” microstructure with curved and intersecting basal planes. The determination of this “fullerene-like” microstructure being responsible of a lower CoF at a nanoscopic scale, could be performed through molecular dynamics calculations.

2.2. Bulk Chemistry—Additives

The changes in the structure, composition and mechanical properties of the film with increasing additive content may take important positions in controlling the film friction and wear behavior. Especially, the bonding ratio of film among several factors, which might take important positions in controlling the wear behavior, would be the main reasons for its low CoF and better wear resistance [33]. It is generally believed that an increase of bonding ratio (sp3/sp2) might increase wear resistance, but separate study is difficult since it is difficult to grow films that vary one of these independently of the other [34]. While the amount of H and the sp3/sp2 bonding ratio influence nanotribology, detailed comprehensive studies necessarily involve varying these parameters independently to elucidate their individual contributions to the mechanical and tribological behavior.

In need of superhard and yet tough ceramic films, a-C-based films prove to be good candidates [35]. Bias graded deposition creates a graded bonding structure such that the sp2 hybridization become more intense towards the substrate-film interface to provide better toughness and adhesion while sp3 bonding gets more intense towards the surface of the film to render higher H for tribological performance. Co-sputtering of Al with graphite embeds elemental Al into a-C to form a-C(Al) film which is reported to greatly reduce growth-induced stresses acquired during deposition, at the expense of H because of the reduction in the amount of sp3 bonding. Co-sputtering of Ti and Al with graphite produces nc-TiC to embed in a-C(Al) matrix, while formation of nc-TiC helps partially restore the hardness lost due to doping of Al. Comparing with a-C film deposited under constant substrate bias, the bias-graded deposition leads to less friction and improves adhesion of amorphous carbon by twofolds [35]. Nanocrystalline TiC embedding in amorphous carbon results in an increase of adhesion up to four times with a slight increase in CoF. The incorporation of Al in the amorphous carbon matrix results in an increase of adhesion strength and reduces the CoF by 20% [35]. Under ambient condition, the nanocomposite films exhibit higher friction than a-C films while under oil lubrication the nanocomposite films experience less friction. For nc-TiC/a-C(Al) film, a low CoF of only 0.04 is revealed. The incorporation of F has been found to alter the hydrophobicity of DLC films, and this also influences the frictional characteristics. Using a Chemical Vapor Deposition (CVD) process, increasing the F concentration increases the water contact angle (from 72–95°, as F content is increased from 0%–35%) [36]. In literature, adhesion and friction measured by Atomic Force Microscopy (AFM) in air decreases with increasing contact angle. The reduced adhesion is attributed to the reduction of capillary interactions, but the presence of a capillary has not been observed directly. Regardless, this demonstrates the important effect that adhesion forces have on nanoscale friction. Numerous significant studies of literature have lead to new perspectives, indicating that for hard carbon systems, surface chemistry dominates the tribology in the wearless regime, while bulk chemistry matters more after the wear threshold has been reached.

In Figure 2 a schematic representation of the CoF ranges for a-C, ta-C, a-CNx and various DLC films along with chemical structure embedded. Data presented in Figure 2 are based on Table 1, where tribological properties of carbon-based thin films deposited by various methods are presented according to literature studies.

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Figure 2. Schematic representation of the CoF ranges for a-C, ta-C, a-CNx and DLC films along with chemical structure embedded, according to Table 1.

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Figure 2. Schematic representation of the CoF ranges for a-C, ta-C, a-CNx and DLC films along with chemical structure embedded, according to Table 1.
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Table 1. Tribological properties of carbon-based thin films deposited by various methods.

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Table 1. Tribological properties of carbon-based thin films deposited by various methods.
Carbon Thin Film TypeDeposition methodThickness (nm)H3/E2 (GPa)H/ECoF at Load (mN)
a-C sp3 rich multilayer [37]MS900.2350.0930.25
a-C multilayer [38]MS1150.3830.1263
a-C sp3 rich [37]MS300.17040.0973
a-C sp2 rich [37]MS300.03030.06150.350.35
a-C sp2 rich [37]EB300.010.05
a-C [37]UBMS0.40870.11480.250.25
a-C:H [39]PECVD11400.22440.125
ta-C [1]S-bend0.6490.1230.05
ta-C [1]FCVA700.37040.1110.1
ta-C:H [40]EC701.3891.1670.01–0.121–20
a-CNx [38]MS2220.21420.1090.1–0.31–20
ta-C [41]FCVA760.89350.10570.1–0.151–20
ta-C [42]PLD1200.07
DLC:Ti [41]CFUMS10000.29440.10560.1–0.41–80
DLC:Mo [43]MS6500.22030.1192
DLC:Silver [44]PECVD5000.17–0.241–20
ta-C [45]FCVA500.25180.070.08–0.141–5
ta-C [46]OPBD-FCVA0.8610.1071
a-CNx [45]MS2800.02740.07
ta-C multilayer [46]OPBD-FCVA0.81370.1440.12
a-C [47]CFUBMS2000.34560.120.1
a-C:H [48]PIII700–0.60–14
a-C:Ti [49]PCVD5000.05–0.11–200
ta-C:Si [46]FCVA50.23
a-CNx [50]FCVA1003.5020.232
a-C [51]Sputtering292.1850.2360.15–0.2525–300
DLC:9Cr18Vacuum Magnetic-Filtering Arc Plasma Deposition5000.1210.0590.15–200–180
DLC:40CrNiMo [52]5000.1850.0640.15–400–84
a-CNx [53]PACVD0.1–0.180.1
a-CNxRF Sputtering PECVD250–4000.1–0.180.1
DLC [54]0.3150.108
DLC:Al2O3-TiC ceramic (AlTiC), DLC:Si (1 0 0),PECVD2500.0990.0620.06150
DLC:fused silica andPECVD0.6870.16250.052
DLC:SU8 photoresist [55]PECVD4.880.43330.045
a-C:F:N:H [56]RF-PECVD0.0470.0790.13
DLC:c-Si [57]PECVD0.2/0.3
a-C (H: 28.1 GPa)DC Magnetron Sputtering1 to 1.6 μm0.15
bias-graded a-C (H: 25.1 GPa)0.14
nc-TiC/a-C (H: 27.4 GPa)0.22
nc-TiC/a-C(Al) (H: 19.6 GPa) [29]0.18
Si-DLC (0 at.%)RFPACVD10001.66322000
Si-DLC (1.0 at.%)10001.0189
Si-DLC (2.0 at.%) [33]10000.5895
Cr/a-C [58]Unbalanced Magnetron Sputter20000.17660.097 0.111
DLC/Ni 50% CrPVD-CVD0.11000
DLC/Al2O3-13% TiO2PVD-CVD0.65
DLC/WC-Co [59]PVD-CVD0.1
DLC [60]Linear Ion Beam2.20.02220.06660.2–12.8
nc-Ti (N,C)/a-C:HPulsed DC 400
31.1 H at.%magnetron0.1370.0990.21
42.6 H at.%Sputtering0.07740.09570.25
47.3 H at.% [61]0.03590.08470.35
Ti-DLC/aluminaClosefieldUnbalanced MS10000.29440.10560.12–0.255–10
Ti-DLC/steel [43]
a-CNx-TiNx/G/Ti ratioPLD1200
Pure Ti0.16130.08720.34
0.5 0.15870.08210.24
1 0.19680.086510.19980
Pure graphite [62]0.20210.08580.11
a-C:H polymerlikeECR-CVD630–11500.0070.05–0.080.4900–2000
a-C:H fullerenelike [63]0.0120.06–0.120.1
aCNx/TiN [64]Pulsed laser depositionaCNx TiN
25 280.26360.09380.28
33 210.19240.08770.16
42 120.17990.08840.13
a-CNx on Ti-TiN/CNx gradient underlayerDirect Current Magnetron Sputtering180500–8500
a-CNx on Ti interlayer0.224010.099560.223
M4 [65]
DLC:silicon [66]0.130.1

2.3. Applied Load Effect

Several single asperity nanotribological studies of carbon-based materials have been performed in the literature [30]. In case of carbon-based measurements, tip selection is mandatory. However, commercial tips are typically composed of diamond, Si or Si3N4, with only a few other coated tips available. Several coated tips are reported in literature; the benefit of film tip with the same material as the sample is the matching of the interface that would be found in an actual device composed entirely of that material. In this case, further modeling and experimental work is required to clarify the exact role that contact area plays at the nanoscale. Despite the important insight into the tribological properties of carbon-based films derived from previous studies, relatively less attention has been paid on the friction behavior and films deformation mode dependence on the applied normal load, especially in the case of carbon-based thin films subjected to low normal loads [67]. The influence of the normal load (from 2 to 20 mN) on the friction of amorphous carbon nitride (CNx) films grown on Si (100) substrates by reactive ion sputtering and energetic ion bombardment during deposition (IBD) is studied in [68]. In Figure 3 the nanotribological performance of carbon-based thin films (dependence of CoF on the applied load), according to Table 1, is presented.

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Figure 3. Dependence of CoF on the applied load for carbon-based thin films, according to Table 1.

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Figure 3. Dependence of CoF on the applied load for carbon-based thin films, according to Table 1.
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The mechanical and tribological properties of ta-C films are closer to those of bulk diamond than the a-C coatings. Hydrogenated a-C films in principle show a higher coefficient of friction than the a-C and ta-C materials due to the significant amount of hydrogen and differentiation of sp3 bonding structures.

The tribological characteristics of interface strongly depend on orientation, topography, chemical composition, bonding structure, elastic/plastic properties, and environment. In case of physical origins of friction and energy dissipation determination, precise measurements of these factors must be considered [32].

Applications involving sliding and/or contacting surfaces require certain properties of film, such as resistance to fracture, low friction and low wear properties, which are determined through measurement of key physical properties such as H, E and surface roughness due to the relationships between these physical and the desired tribological properties. Film adhesion and fracture susceptibility of the film-substrate couple is commonly determined through scratch test for critical load investigation.

2.4. Orientation Effect in Crystalline Diamond

At the macroscopic scale, diamond single crystals show strong orientation effects (friction and wear depend on both the surface orientation and the sliding direction), whereas at the nanoscale the findings are considerably different (attributed in part to wear avoidance, but it may also be as a result of an enhanced influence of local atomic interactions). In several studies performed on single-crystal, H-terminated diamond (111) and (001) surfaces with a quite low diamond tip radius, no difference in average friction force values was observed between the two surfaces except for qualitative differences in the friction images, attributable to the different lattice spacing and orientations [69,70].

The high CoFs of rough diamond films with (111) orientation can be attributed to the abrasive cutting and plowing effects of sharp surface asperities on the softer counterface pins. If a favorable (100) growth orientation is present, such films can also afford low CoFs to sliding surfaces, despite relatively higher measured surface roughness. In general, previous studies confirmed that regardless of the grain size, diamond films with a smooth surface finish provide very low friction to sliding counterfaces. Apart from physical roughness and chemical passivation effects, phase transformation or structural changes can also play a major role in the friction and wear performance of carbon thin films. The extent of such changes can be dominated by environmental species or by ambient temperature. Phase transformation can readily occur even in natural diamond [71] when extreme contact pressures and/or high frictional heating are present at local asperity levels. Real contact occurs first between these asperities, and their tips can either fracture or undergo phase transformation because of the extreme pressures and high frictional heating. Thermodynamically, graphite is the most stable form of C, whereas diamond is metastable. It is also known that when excited thermally or by ion bombardment, diamond can transform to a graphitic form [72,73]. The graphitic debris particles can gradually accumulate at the sliding contact interface and then begin to dominate the long-term sliding friction and wear performance of these films. Most of the debris particles derived from sliding diamond surfaces exhibit a graphitic microstructure [39,40]. Raman Spectroscopy, Electron Diffraction, Electron Energy Loss Spectroscopy, and Transmission Electron Microscopy have concurrently confirmed the presence of highly disordered graphitic debris particles at sliding contact interfaces [39].

2.5. Film Thickness Effect

The wear rate reduces with increasing applied load and more significantly with reducing carbon based thin film thickness. In certain cases a clear exponential reduction of specific wear rate with reducing film thickness over the range of 2000–10 nm occurs. The initial film thickness is of importance, since wear rate of thick films is not reported to decrease exponentially as the substrate approaches [74]. While a little change in film H and E with film thickness is revealed, the main mechanism of wear operating is ascribed to three-body abrasion, although fatigue fracture is thought to significantly contribute.

2.6. Film Roughness Effect—Lubricant Use

Although RMS surface roughness does not carry any information about slopes, sizes or frequencies of asperities, it is still an important parameter for predicting and understanding the properties of tribological systems [75]. Previous investigations with carbon films indicated that CoF increases with increase of roughness [76,77]. Extensive studies of friction dependence on the surface roughness report an increase, over a wide range of surface roughness, in the CoF with very smooth or very rough surfaces. Friction coefficient increase is attributed to real contact area excessive growing, whereas in the latter it is due to the need to lift one surface over the asperities of the other. In intermediate ranges of roughness, friction is at its minimum and does not depend on the roughness. In a ratchetting mechanism, relative motion between two surfaces is achieved by asperities riding over each other (asperities slope angle increase), leading to increase of CoF with increasing roughness [76]. In energy-loss mechanism, asperities push each other, resulting in increased CoF with roughness. In case of film surface polishing for roughness reduction, the film does not contain any such carbonaceous layer to transfer (friction coefficient does not vary with addition of lubricant). Additives are easily adsorbed on the surface of the film and able to form boundary lubrication, which is independent of the quality of the additives as the film is nanocrystalline and contains an exceptionally high amount of surface atoms. In case of higher temperature, adsorbed additives diffuse to the bulk of the film. In this case, presence of high amount of grain boundary and higher temperature augment the process of diffusion. The characteristic of the adsorbed boundary layer is altered and its functional structure and lubrication abilities are lost. When contact temperature is low, less diffusion of additives of the lubricant occurs to the bulk of the film and boundary lubrication forming with line contact is easier. If temperature rises at the contact point with ball contact, additives tend to diffuse to the bulk of the film due to high amount of grain boundary in nanocrystalline film. Thus, formation of boundary lubrication becomes difficult giving rise to increase in friction coefficient [78].

Figure 4 shows that ta-C films have ultra-low roughness (RMS roughness ~0.12 nm) and that are independent of the film’s thickness, thus providing films equally smooth when 11 or 60 nm thick. These are unique properties since films usually form through a series of stages of nucleation, coalescence and possible roughening which, in general, lead to island formation for the thinnest films.

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Figure 4. Correlation of roughness and thickness of ta-C films deposited with HCA and FCVA.

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Figure 4. Correlation of roughness and thickness of ta-C films deposited with HCA and FCVA.
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2.7. Graphite—Superlubricity Effect

When a tip is sheared over the surface of a crystal lattice, it often moves in an unstable “stick-slip” pattern that matches the lattice. This was first observed on graphite and has since been reported on many other materials including diamond [79], and it is attributed to energy storing of the compliance of the system (cantilever, tip, and contact zone) as shear is applied. When the lateral force (gradient in the sliding direction) drops below the net system stiffness, the essence of mechanical instability leads to sudden energy release. As lateral interaction force is necessarily periodic by virtue of the symmetry of the crystal surface, stick-slip behavior repeats once every lattice site, creating stunning images that match the lattice periodicity. In this case, the remaining frictional dissipation [70,80,81,82] is below recordable values and the phenomenon has been labeled (perhaps misleadingly) “superlubricity” (friction is dramatically lower). A key to achieve this transition to instability-free low friction is to obliterate the periodicity of the lateral potential by making the interface incommensurate. When deposited on atomically smooth or highly polished substrates (such as Si wafers or cleaved sapphire or mica surfaces), carbon films can attain the kinds of smoothness that are needed for eliminating the deleterious effects of surface roughness on friction. At thicknesses as low as 2–5 nm, they provide very uniform coverage and mimic the original surface roughness of the underlying substrates. If necessary, the sliding surfaces of carbon films can be polished after the deposition. As for achieving a high degree of chemical inertness on sliding carbon surfaces, researchers have pursued two complementary or closely-related approaches. Specifically, they have either used a hydrogen-rich gas discharge plasma during film deposition [70,79,81,82,83,84,85,86,87,88] or they have introduced hydrogen gas into the test chamber during tribological testing [88,89,90,91,92,93]. The control of surface chemistry or chemical interactions at sliding DLC interfaces is extremely important for the friction and wear behavior of carbon-based thin films. Specifically, by controlling or effectively eliminating the intrinsic and extrinsic sources of friction in carbon films, one should be able to achieve ultra- and superlow CoF under both dry and lubricated sliding conditions [94].

2.8. Effect of Environment

Tribochemical reactions do occur, but physisorption of environmental species also plays a role [30]. An understanding of humidity effect of these materials nanoscopically is only beginning to emerge. Adhesion shows no dependence on relative humidity (RH), indicating that the conventional picture of meniscus formation leading to higher friction and adhesion does not represent the mechanism at play in this system, as the adhesion should change with RH. Using hydrocarbon-coated tips, the frictional properties of diamond and amorphous carbon are found to differ between air (at 40%–60% RH) and dry Ar environments. Interfacial shear strengths are reported to be highest for a-C in air, followed by diamond in air, then a-C in dry Ar, and finally diamond in dry Ar (adhesive forces are also lower subjected dry Ar environment). Higher friction in ambient conditions is attributed to the presence of water on the surface of the samples [30]. Wear and frictional behavior of carbon-based films rubbed against brass in water are reported to be affected by the water temperature and dissolved ions. Elevated temperature with frictional heat generation prevents the formation of intact and lubricious tribo-layer leading to higher friction and wear [95]. When adsorbed gases are removed from sliding diamond surfaces, friction increases rapidly because the dangling surface bonds are free and highly activated to form strong bonds across the sliding contact interface. Despite a large discrepancy in time and length scales, molecular dynamics simulation has provided significant insight into the extent of physical, chemical, and mechanical interactions that occur at sliding diamond interfaces on the atomic scale [1].

Sliding friction forces at nanometer scale are determined by two competitive processes. The first process is the thermally activated stick and slip behavior when friction is attributed to the adhesive forces between the two surfaces in contact. Additionally, capillary effects due to water vapor condensation must be taken into consideration, especially for tests performed in air.

2.9. Effect of Substrate Material, Thickness and Roughness

Other important factors are film thickness, substrate roughness, and substrate stiffness, as reported in literature [55,96,97,98,99]. For hard carbon films on substrates, of particular interest for hard-disk applications, numerous groups have reported that a critical film thickness (usually >5 nm) needs to be achieved for the film to exhibit the exceptional nanoscale friction and wear properties known to these materials [94]. Furthermore, the roughness and E of the substrate can affect film properties. Consequently, according to the conformal way in which carbon films coat a substrate, substrate roughness is transferred to the film. Lower E of the substrate can lead to bending under applied loads, which in turn may increase contact area and thus friction [55]. When film thickness reaches a practical lower limit, determining the intrinsic properties and likewise the functionality of the films for wear- and corrosion-resistant applications poses a challenge. The final film roughness of carbon films strongly depends on the surface roughness of the substrate. The films deposited on substrates with relatively low surface roughness showed an increase in the final film roughness values, due to the higher deposition rate at the peaks and the lower lateral growth at the valleys [100]. It has been observed that the formation of radial cracks precedes ring cracks in carbon films on the rougher steel substrates. Ring crack formation was delayed, and happened at higher loads for the rougher samples, due to the early formation of the radial cracks at the film-substrate interface, coupled with the plastic deformation of asperities on the surface of the film. The population of radial cracks at the interface of film and substrate is proportional to the relative substrate surface roughness, i.e., on the distribution of interfacial asperities.

2.10. Tribological Properties: The Significance of Ratio H/E

It is known that many of the mechanisms of film failure begin with or directly involve plastic deformation. Consequently, a particular concern in the usefulness of a-C films as protective overcoat materials in hard disk and/or wear-resistant applications is that these films must be highly resistant to plastic deformation during contact events [1]. The film has to undergo a high proportion of elastic deformation occurring when indenting, resulting in high values of H (which reflect the small amounts of plastic deformation occurring), and not only high H as is generally held. One possible way to extract the elasticity can occur via Johnson analysis for solids of revolution [101,102], taking into account the Tresca criterion (p0 = 1.6Y, where Y is the yield stress) and the Tabor relation (H = 3Y), the load (Py) to initiate the yield (plastic deformation) is proportional to the term (H3/E2): Py = K(H3/E2). The term H3/E2 combines the H and E values of a material and sets the amount of elasticity exhibited by the film [1,102]. In Figure 5 and Figure 6 schematic representations of the H3/E2 (1.0 for diamond) and H/E (0.1 for diamond) correlated with CoF are presented (according to Table 1), respectively.

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Figure 5. Schematic representation of the H3/E2 correlated with CoF for four types of carbon thin films.

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Figure 5. Schematic representation of the H3/E2 correlated with CoF for four types of carbon thin films.
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Figure 6. Schematic representation of the H/E correlated with CoF for four types of carbon thin films. Line is guide to the eye.

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Figure 6. Schematic representation of the H/E correlated with CoF for four types of carbon thin films. Line is guide to the eye.
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Ranking of materials according to their H/E ratio can provide extremely close agreement to their ranking in terms of wear, as reported in literature [103]. Whilst many researchers have, over the years, confirmed the importance of high H in mitigating wear, the case for a reciprocal relationship between wear resistance and E is less well-proven. Despite the lack of conclusive evidence for a need to enhance elasticity (i.e., to reduce E) in order to improve wear resistance, the intuitive logic of this route has remained, returning to the H/E ratio as a ranking parameter [103]. The ratio of H to E appears in the so-called “plasticity index”, which is widely quoted as a valuable measure in determining the limit of elastic behavior in a surface contact, which is clearly important for the avoidance of wear [103]. The H/E as an indicator of film durability is related to the elastic strain to failure capability (and resilience) of a candidate material [104], regarding the need for tribological films to accommodate some degree of substrate deformation.

2.11. Nanoscale Contact Mechanisms Using Atomistic Simulations

All factors presented above (see 2.1–2.10), which determine nanotribological behavior of carbon based thin films, have been studied extensively during the last decade using atomistic simulations [105,106,107,108,109,110,111,112,113,114]. Atomistic simulations based on MD have immersed as alternative in order to explain friction and transitions between different mechanisms of carbon based films, since analytical models based on continuum mechanics fail to explain friction behavior at the nanoscale. In addition, main computational parts of multiscale tribological calculations for friction and lubricity are based on MD simulations [105].

The definition of the contact edge becomes ambiguous when the atomistic nature of the interface dominates its physical behavior [106,107,108].

The cohesive energies and chemical reactions of hydrocarbon systems as well as the elastic constants of solid carbon-based materials are accurately described by the Reactive Empirical Bond-Order (REBO) potential [109]. The range of the REBO potential extends as far as the chemical interactions and does not include dispersive forces. The van der Waals interactions are therefore integrated with REBO using an analytical switching function in the regime where the two potentials overlap.

Mylvaganam et al. [110] conducted MD simulations to study the behavior of carbon-diamond, graphite and carbon nanotube-on contact sliding against a diamond asperity vacuum. It was found that, on the nanoscale, graphite and carbon nanotubes exhibit low coefficients of friction, while carbon nanotubes act as a better solid lubricant with a friction coefficient of only about 0.03 in vacuum on the nano/micro scales. The mechanisms of the difference in frictional properties of the three forms of carbon at different dimensional scales were due to the difference in their atomic structures [110]. Gao et al. [27] used MD simulations in order to explore film thickness, counterface termination, and long-range interactions on tribological properties, identifying detailed tribochemical reactions and their effect on friction and wear. Τhe thickness of the amorphous films had no influence on the calculated friction, proving that the structure of the film near the interface is what is dominating the friction. Additionally, the simulation results suggested that the structure of the film, especially the sp3-to-sp2 ratio, could profoundly affect the tribological properties of the film. Films that contain a larger fraction of surface sp2-hybridized carbon will exhibit higher levels of friction than those films with more surface sp3-hybridized carbon; this increase in friction is attributed to the increased adhesion from tribochemistry. It should also be noted that changing the sp3-to-sp2 ratio within a carbon film will also change its hardness and may also change the film’s phonon frequencies. Adhesion, due to the bonding between a carbon on the counterface and a carbon in the film, contributes significantly to the friction. While adhesion between the probe and the film increases the calculated friction; tribochemical reactions within the film lead to a restructuring of the film and a reduction in friction [27]. In addition, there is actually no standard that relates adhesion and friction, which means that range of expected reduction in friction per unit reduction of adhesion is not known [28]. Recently, the first analytical model that can describe the interplay between adhesive forces at the interface and subsurface plastic deformation for single-asperity sliding contacts has been developed by Maneesh Mishra et al. [111]. As it is referred by Bhushan et al. [112] adhesion is the main contribution to the friction for nanoscale experiments.

MD simulation studies conducted by Zhang et al. [113] on hydrogenated carbon (CHx) films showed the reduction of friction coefficient with surface hydrogenation. These results suggest that pulsed DC magnetron sputtering can produce CHx films with friction properties similar to those obtained by plasma-enhanced CVD [113].

The hydrogen concentration is crucial for the running-in behavior and the resulting steady-state friction coefficient of a-C: H tribo-contacts [114]. Similar observations on running-in have been made previously by Gao et al. [27]. Two passivation mechanisms and an explanation of the observed sp3 to sp2 transformation, which is seen under dry as well as lubricated sliding can be extracted from MD simulations performed by Pastewka et al. [114]. An obvious strategy for reducing friction is to reduce the strength of interatomic interaction between the surfaces, which can be done by surface treatment with the intention of reducing the free surface energies, for example, or by deliberately choosing weakly adhering materials. This is not unlike the macroscopic strategy of lowering friction by selecting metallurgically incompatible materials [28]. MD simulation methods are useful to gain insight for nano-scale interactions and obtain quantitative results for various system models and operating conditions. However, there are still several problems that need to be tackled to obtain simulation results that are closer to the real world [6].

3. Conclusions

Due to very unique structures, attractive properties and performance characteristics of carbon based thin films, both the scientific and industrial communities are drawing significant attention to their synthesis, processing and functionalization. Dedicated scientific studies on carbon-based thin films in recent years have led to the development of more exotic versions consisting of unique nanophases and/or structures. Tetrahedral amorphous carbon films are good candidates, among other types of carbon-based films, in terms of the best combination of high H and E values, lower CoF, highly elastic deformation under static nanoindentation testing and nanoscratching up to relatively high normal loads and plastic deformation for high normal loads, however without evidence of film failure. Table 1 summarizes the results of experimental techniques on nanotribological properties of carbon based films.

Connection of the nano-, micro- and macro-scale tribological behavior in terms of experiments (better control and accurate description of the nanoidentation and atomic force microscopy tips) and computational techniques of the tribological interaction of the carbon-based materials remains a challenge. Studies on origin of friction, adhesion, wear and other tribological features at the atomic scale, since they are highly dependent on the surface interactions, using sophisticated experimental and computational tools should be continued in order to provide a deeper understanding of friction in nanoscale. MD simulation methods are useful to gain insight for nano-scale interactions and obtain quantitative results for various system models and operating conditions. However, there are still several problems that need to be tackled to obtain simulation results that are closer to the real world. Table 2 summarizes simulation conditions, used material and results from molecular dynamics techniques applied on carbon based thin film structures in order to study mechanisms of friction and lubricity.

Table 2. Summary of molecular dynamic simulations of carbon based films nanotribological systems.

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Table 2. Summary of molecular dynamic simulations of carbon based films nanotribological systems.
YearSimulation conditionUsed materialsResults
1999 Cagin et al. [115]Brenner’s potentialBare diamond hydrogenated diamondDangling bond of surface caused higher friction force
2002 Gao et al. [27]Brenner’s reactive empirical bond-order potential (REBO)Hydrogen-terminated diamond (111) counterfaces are in sliding contact with diamond (111) surfaces coated with amorphous, hydrogen-free carbon filmsEffects of film thickness, adhesion, and long-range interactions
2004 Sulin Zhang et al. [113]Tersoff-Brenner formHydrogenated carbon films (CHx)Determine how surface hydrogenation affects friction coefficient
2010 Pastewka et al. [114]Modified Brenner’s reactive empirical bond-order potential (REBO)Diamond-like carbon (DLC) coatingsAtomistic insights into the running-in, lubrication, and failure of hydrogenated diamond-like carbon coatings
2010 Mylvaganam et al. [110]Many-body Tersoff-Brenner potentialCarbon-diamond, graphite and carbon nanotubeNanotubes are the best solid lubricant as it has a low coefficient of friction that can be maintained across any dimensional scales from nano to macro scales due to the large aspect ratio of length to diameter
2012 Bucholz et al. [116]Brenner’s reactive empirical bond-order potential (REBO) coupled with a Lennard-Jones (LJ) potentialCarbon nano-onionsThe ability of the nano-onions to roll is inhibited both by increased contact pressure and the presence of a diamond core within the nanoparticles that enhances the formation of interfacial bonds during friction


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