Researches

■ Three-Dimensional Coating of a-C:H Films using Bipolar PBII&D (Inner surfaces of the trench, slit, hole, pipe....)

Bipolar plasma-based ion implantation and deposition (bipolar PBII&D) has been recognized as a promising technique for coating deposition on complex three-dimensional targets. As the target is fully immersed in the plasma throughout the process, the plasma sheath can be formed with a quite high conformability around the target. In this study, a-C:H film was deposited on a micro-trench pattern by using bipolar PBII&D, and the structure of the a-C:H film across the overall surface region of the trench was examined by making use of their corresponding Raman spectra. The two types of negative high voltage pulses were applied to the targets for comparison: -0.5 and -15 kV. The scale of micro-trench used in the study is much smaller than that of plasma sheath produced under these negative voltages (about 1cm and 14cm for -0.5kV and -15kV, respectively). The plasma behavior (i.e., ion flux, impact angle and energy) in the surrounding of the micro-trench was calculated with Particle-In-Cell Monte Carlo Collision Method (PIC-MCCM). As a result, a-C:H film was successfully coated on the overall surface of the trench. When the applied negative voltage was -0.5 kV, the structure of a-C:H film coated on the sidewall of the trench became more polymer-like carbon (PLC) than those of the top and bottom surfaces did. This, as indicated by the simulation results, is because the ions, which strike the sidewall, tend to have less incident energy. Whereas in the case of -15 kV, the a-C:H film on the sidewall was more graphite-like carbon (GLC) film, despite of its smaller incident ion energy in comparison to those of the top and bottom surfaces. This phenomenon is attributed to the sputtering effect from the bottom surface of the trench, as evidenced by the plasma simulation.

 Schematic of PBII and a-C:H coating on a 3D target

 a-C:H coating on a micro-scale mold

■ DLC-Based TENG (Triboelectric Nanogenerator)

Modern electronic systems are smarter and compact, yet highly efficient at greater speeds. These systems require just a minimal amount of power which have indeed encouraged new technologies to scavenge energy from the surrounding environment. Triboelectric nanogenerator (TENG) is one such device which has demonstrated a cost-effective, reliable and efficient technology for harvesting natural mechanical energy. However, the durability and stability of TENG is a critical attribute for the high output efficiency at a consistent rate and strongly depends on the frictional characteristics of triboelectric materials. In the first of its kind, a detailed investigation is done on the ability of diamond-like carbon (DLC) film to be a potential triboelectric material for TENG applications. DLC film was deposited on the substrate (electrode) of a contact-separation based TENG (CS-TENG) using plasma-based ion implantation and deposition (PBII&D) technique. The performance evaluation of TENG consisting of DLC film - polymer as the triboelectric pairs revealed some very interesting results. Hydrogenated DLC (H-DLC) and PTFE (Polytetrafluoroethylene) based TENG produced the highest output with a peak current of 3.5 μA and a power density of up to 57 mW/m2 over other conventional dielectric pairs like Al-PTFE, Polyimide (Kapton®)-PTFE, and Kapton-Al. Furthermore, fluorine doped DLC (F-DLC) film produced a moderate output with Kapton, and PTFE, indicating its benefits for TENG applications. In the durability assessment, the DLC deposited rotary sliding-TENG exhibited excellent durability by producing a stable output current for 3 h at a reduced friction coefficient. This study serves as a noteworthy beginning towards the understanding of the triboelectric behavior of DLC films from TENGs perspective and could significantly contribute to designing of a highly durable, cost-effective, low friction and efficient sliding-TENG.

■ Tribological Properties of a-C:H Films

The tribological properties of a-C:H films were investigated from a microstructural point of view. The microstructures of a-C:H films (i.e., diamond-like, polymer-like, and graphite-like structure) were analyzed by Raman spectroscopy. Friction tests were conducted under controlled relative humidity. At low humidity condition, diamond-like-structured film having a high hardness shows a high friction coefficient due to the surface chemistry dominated by iron oxides from the counterface, and the friction coefficient decreases as the structure of a-C:H film becomes more polymer-like or graphite-like. At a higher humidity condition, the friction behavior of a-C:H film against steel ball is a trade-off of the effects of iron oxide formation and water lubrication. The friction coefficient increases by the formation of abundant iron oxides and simultaneously decreases by the water lubrication, resulting in an almost constant friction coefficient except for the highly polymer-like carbon film, whose friction coefficient increased with increasing relative humidity.

■ Structural Analysis of a-C:H Films

In the present study, a-C:H films were prepared by bipolar plasma based ion implantation and deposition (PBII&D), and the structural and mechanical properties of the a-C:H films deposited on Si substrates were evaluated by Raman spectroscopy. In the PBII&D processing, the positive and negative pulse voltages were varied from 1 to 3 kV and from −1 to −15 kV, respectively. With an increase in the pulse voltages, the Raman G-peak position and I(D) / I(G) ratio increased, and the G-peak full width at half maximum (FWHM(G)) decreased, indicating graphitization of the a-C:H films. In the low wavenumber regime, the FWHM(G) increases when the G-peak shifts to higher wavenumbers, reaching a maximum value at around 1540 cm−1, and then decreases. This behavior was due to the structural changes occurring in the a-C:H films with an increase in the wavenumber. Diamond-like carbon (DLC) to polymer-like carbon (PLC) transition occurred in the low wavenumber regime, and DLC to graphite-like carbon (GLC) transition occurred in the high wavenumber regime. Further, two different trends were observed in the relationship between the mechanical properties (hardness, elastic modulus, and internal stress) of the DLC films and the FWHM(G), originating from the structural change from DLC to GLC and PLC.

■ Superhydrophobicity of Hard Solid Surface

■ Ultra-Low Friction Properties of Graphene Films

■ Self-Assembled Monolayers (SAM) on a-C:H Films

Self-assembled monolayers (SAMs) of 1H,1H,2H,2H-perfluorodecyltriethoxysilane were deposited on the magnetic hard disk surface by immersion. SAM formation was confirmed by contact angle measurement, ellipsometry, and x-ray photoelectron spectroscopy. The friction of unlubricated, SAM-coated and perfluoropolyether(PFPE)-coated disk surfaces was measured with lateral force microscopy, spin-stand tester and scratch tester. The SAM-coated disk surfaces had lower friction as compared to the unlubricated disk surfaces. This result is in agreement with the hydrophobic nature of the SAM-coated surface. On the other hand, the friction of the SAM-coated surface was larger than the 2-nm-thick PFPE-coated surface, even though the hydrophobicity of the SAM-coated surface was higher than that of the PFPE-coated surface. This would be attributed to the mobility of the multilayered PFPE lubricant, whereas the friction of SAM-coated surface showed comparable or even better compared to that of 1.1-nm-thick PFPE-coated surface which had a small mobile portion.