Blood compatibility of La2O3 doped diamond-like carbon films

La₂O₃ doped diamond-like carbon films (DLC) with different concentration were deposited by using Radio-Frequency magnetron sputtering. The microstructure and surface properties of DLC films were characterized by Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), and contact angle test. The blood compatibility of the samples was evaluated by tests of platelet adhesion. Results show the sp²-bonded C content increases with increasing of La₂O₃ concentration doped. A remarkable decrease of platelet adhered on the surface of the La₂O₃ doped DLC films was observed comparing to the Chrono flex used in clinical application, suggesting that La₂O₃ doped DLC is able to enhance its blood compatibility. The mechanism of hemocompatibility of doped films was discussed. Our results demonstrate that La₂O₃ doped DLC films are potentially useful biomaterials with good blood compatibility.     

Microstructure and mechanical properties of CeO2 doped diamond-like carbon films

A kind of rare earth oxide, CeO₂, was doped into the diamond-like carbon (DLC) films with thickness of 180–200 nm, using unbalanced magnetron sputtering. All the adhesion strength of CeO₂ doped DLC films is increased, while the residual compressive stress is obviously decreased compared to pure DLC film. Specially, the residual compressive stress of the deposited films are reduced by 90%, when the CeO₂ content is in the range of 5–7%, from a value of about 4.1 GPa to 0.5 GPa. When the CeO₂ content is increased to 10%, the deposited films possess the highest adhesion strength of 85 mN, 37% higher than that of pure DLC film. The nanohardness and elastic modulus exist a transition point at 8% of CeO₂ content within the DLC film. Before this value, nanohardness and elastic modulus of CeO₂ doped DLC films are lower than those of pure DLC film, and after this value, they are higher or adjacent to those of pure DLC film. Auger electron spectroscopy shows a more widened interface of 6% CeO₂ doped DLC film compared to pure DLC film. The enhancement of adhesion strength is mainly attributed to the widening of the film-substrate interface, as well as the decrease of residual compressive stress.     

Structure and mechanical properties of oxygen doped diamond-like carbon thin films

In this study, structure and mechanical properties of doped diamond-like carbon (DLC) films with oxygen were investigated. A mixture of methane (CH₄), argon (Ar) and oxygen (O₂) was used as feeding gas, and the RF-PECVD technique was used as a deposition method. The thin films were characterized by X-ray photoelectron spectroscopy (XPS), Raman spectroscopy (RS), attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FTIR) and a combination of elastic recoil detection analysis and Rutherford backscattering (ERDA-RBS). Nano-indentation tests were performed to measure hardness. Also, the residual stress of the films was calculated by Stoney equation. The XPS and ERDA-RBS results indicated that by increasing the oxygen in the feeding gas up to 5.6 vol.%, the incorporation of oxygen into the films' structure was increased. The ratio of sp² to sp³ sites was changed by the variation of oxygen content in the film structure. The sp²/sp³ ratios are 0.43 and 1.04 for un-doped and doped DLC films with 5.6 vol.% oxygen in the feeding gas, respectively. The Raman spectroscopy (RS) results showed that by increasing the oxygen content in doped DLC films, the amount of sp² CC aromatic bonds was raised and the hydrogen content reduced in the structure. The attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FTIR) confirmed the decrease of hydrogen content and the increase the ratio of CC aromatic to olefinic bonds. Hardness and residual stress of the films were raised by increasing the oxygen content within the films' structure. The maximum hardness (19.6 GPa) and residual stress (0.29 GPa) were obtained for doped DLC films, which had the maximum content of oxygen in structure, while the minimum hardness (7.1 GPa) and residual stress (0.16 GPa) were obtained for un-doped DLC films. The increase of sp³ CC bonds between clusters and the decrease of the hydrogen content, with a simultaneous increase of oxygen in the films' structure is the reason for increase of hardness and residual stress.     

Influence of nickel oxide nanolayer and doping in organic light-emitting devices

Here we report the effect of introducing nickel oxide (NiO) on the performance of organic light-emitting devices (OLEDs) based on small molecules. For the purpose of aligning the NiO deposition with the conventional OLED process, we employed a thermal evaporation method using the NiO powders. To understand the influence of the NiO introduction, we fabricated two types of devices: (1) OLED with the NiO nanolayer and (2) OLED with the NiO-doped hole transport layer. Results show that the NiO introduction improved the hole injection in both types of OLED. However, the device with the NiO nanolayer exhibited greatly improved efficiency, whereas the efficiency was significantly lowered for the device with the NiO-doped hole transport layer.     

掺杂聚乙烯基咔唑的螺噁嗪光致变色的性能

将PVK(聚乙烯基咔唑)以不同的比例掺杂至螺噁嗪光致变色化合物的体系中,通过对螺噁嗪开环体紫外-可见光谱和聚乙基咔唑荧光光谱的分析可以得出,掺杂体系中聚乙烯基咔唑中的电子空穴可容纳螺噁嗪光致变色过程中迁移的电子,从而提高了螺噁嗪开环的效率。     

Electrodeposition mechanism of hydrogen-free diamond-like carbon films from organic electrolytes

A brief introduction on the development of electrodeposition of diamond-like carbon (DLC) films was given, and our experiments were done, emphasizing on how to deposit hydrogen-free DLC films. Methanol, acetonitrile and N,N-dimethyl formamide (DMF) were chosen as electrolytes, while Si and conductive glass were used as substrates. The sample deposited on Si through methanol was the only one in this comparative research that produced hydrogen-free DLC film as it was indicated by the FTIR spectroscopy. Two explanations, based on reaction mechanism, were proposed to explain this fact. It was believed that the reaction rate and the effect of hydroxyl groups in the molecules of the electrolytes played important roles in the deposition of hydrogen-free DLC films.     

Encapsulation of organic light-emitting devices by means of photopolymerized polyacrylate films

For encapsulation of organic light-emitting devices (OLEDs) built on glass substrate, photopolymerizable blend consists of pentaerythritol triacrylate (PETIA) and HSP188 (photoinitiator) was spin-coated onto an OLED and then cured to form a cross-linked passivation layer. The electroluminescence (EL) and the rate of degradation were examined to compare the electrical and the emissive properties of the device before and after forming the passivation layer. In this case, wet process encapsulation, which did not influence the EL characteristic of the device, enhanced the lifetime of the device in air.     

Formation of diamond-like carbon by fs laser irradiation of organic liquids

The high intensities generated in femtosecond (fs) laser interactions offers the possibility of novel formation routes for diamond and diamond-like carbon materials. Coulomb explosion, a common phenomenon in intensive fs irradiation, has recently been shown to lead to a direct graphite–diamond phase transition on the surface of graphite. In this paper we report the results of fs irradiation of a variety of liquid organic compounds at intensities in the Coulomb explosion regime. The products of laser-induced chemistry under these conditions have been studied using visual/surface enhanced Raman and transmission electron microscopy (TEM). Surface enhanced Raman spectra/TEM show that an intermediate diamond phase, trans-polyacetylene chains and amorphous carbon are present after fs irradiation of liquid alkanes. We also find that the diamond component can be enhanced by irradiation in the presence of certain transition metals; however the origin of this effect is still uncertain. Diamond films deposited in this way are found to exhibit a nano-assembled structure involving individual nanodiamonds extending over an area of about 1 cm². This process represents a wet chemical method for room temperature formation of diamond-like carbon films     

Surface energy,wettability, and blood compatibility phosphorus doped diamond-like carbon films

There is an increasing interest in developing novel coatings to improve the biocompatibility of cardiovascular implants. In this work, we fabricated phosphorus-doped (P-doped) diamond-like carbon (DLC) films by plasma immersion ion implantation and deposition (PIII and D) and the structure, physicochemical characteristics, electrical properties, as well as surface biomedical compatibility, were evaluated using different characterization techniques. Microstructures manifesting as dots are visible under optical microscopy while atomic force micrographs disclose that these round and flat islands are distributed evenly on the film surface. Auger electron spectroscopy (AES) and X-ray photoelectron spectroscopy (XPS) results show that they are composed of C, P and O while only C and O can be found in the areas away from the islands. Attenuated total-reflection Fourier transform infrared spectroscopy (ATR-FTIR) spectroscopy indicates the presence of many PO_x and CP_xO_x species. In the Raman spectra, the G peak of the P-doped sample shifts to a lower wave-number suggesting that the film is more disordered. The P-doped DLC film exhibits excellent wettability (16.9° water contact angle). In vitro platelet adhesion and coagulation factor experiments were conducted to examine the blood compatibility. Scanning electron microscopy (SEM) and optical microscopy reveal a significant decrease of the number as well as activation of platelets on the P-doped DLC film.     

Diimide nanoclusters play hole trapping and electron injection roles in organic light-emitting devices

We report thermally stable diimide nanoclusters that could potentially replace the conventional thick electron transport layer (ETL) in organic light-emitting devices (OLEDs). Bis-[1,10]phenanthrolin-5-yl-bicyclo[2.2.2]oct-7-ene-2,3,5,6-tetracarboxylic diimide (Bphen-BCDI) was synthesized from the corresponding dianhydride and amine moieties, and its purified product exhibited a high glass transition temperature (232 °C) and a wide band gap (3.8 eV). The Bphen-BCDI subnanolayers deposited on substrates were found to form organic nanoclusters, not a conventional layer. The OLED made with a subnanolayer of Bphen-BCDI nanoclusters, instead of a conventional ETL, showed greatly improved efficiency (about 2-fold) compared with an OLED without the diimide nanoclusters. The role of the BPhen-BCDI nanoclusters was assigned to hole trapping and electron injection in the present OLED structure.     

Characteristics of nitrogen doped diamond-like carbon thin films grown by microwave surface-wave plasma CVD

Nitrogen doped diamond-like carbon (DLC:N) thin films were deposited on p-type silicon (p-Si) and quartz substrates by microwave (MW) surface-wave plasma (SWP) chemical vapor deposition (CVD) at low temperature (< 100 °C). For films deposition, argon (Ar: 200 sccm), acetylene (C₂H₂:10 sccm) and nitrogen (N: 5 sccm) were used as carrier, source and doping gases respectively. DLC:N thin films were deposited at 1000 W microwave power where as gas composition pressures were ranged from 110 Pa to 50 Pa. Analytical methods such as X-ray photoelectron spectroscopy (XPS), UV-visible spectroscopy, FTIR and Raman spectroscopy were employed to investigate the chemical, optical and structural properties of the DLC:N films respectively. The lowest optical gap of the film was found to be 1.6 eV at 50 Pa gas composition pressure.     

White light emission obtained by direct color mixing in multi-layer organic light-emitting devices

Three different structures of multi-layer organic light-emitting devices, which consisted of two emitting layers separated by a carrier blocking layer, were investigated. Since the emitting layers are constructed to emit different colors, the colors emitted from the structures are mixed. It was found that the colors were directly mixed in the structures of this study due to the carrier blocking layer sandwiched by the two emissive layers. The blocking layer splits the carrier recombination zone, and with the emission color is controlled by balancing the split. For the white light the CIE coordinate of (0.30, 0.33) is obtained at an applied voltage of 14 V. The luminance is measured to be 1,000 cd/m² at 14 V. with the power efficiency of 0.4 lm/W. For a luminance of 100 cd/m² at 11 V., the CIE coordinate is found to be (0.31, 0.34) and the power efficiency was as high as 0.53 lm/W.     

Effects of environmental conditions on fluorinated diamond-like carbon tribology

The effects of environmental conditions and fluorine content on friction of diamond-like carbon (DLC) films are determined and discussed. Relative humidity (RH) has a considerable effect on friction values, modifying them up to a factor 2. Two regions of RH are found, depending on its effect over friction. From 20% to 60% of RH, friction decreases probably due to a better substitution of superficial atoms by hydrogen. From 60% to 80% friction remains stable and equal for almost all samples. A possible explanation would be the formation of a physisorbed layer of water on the surface, which would mask the relatively small chemical and structural variations of the films. Moreover, the different components of surface free energy (SFE) are determined using Van Oss–Chaudury–Good model. The results clearly indicate the importance of Lifshitz–Van der Waals component on SFE and the small correction that supposes acid-base interactions. According to this model, the studied DLC is a monopolar basic material. The basic component is reduced when F content is increased.     

Effects of pulse duration in laser processing of diamond-like carbon films

Experimental studies of the interaction between amorphous hydrogenated carbon (a-C:H) film and short and ultrashort laser pulses in the near-infrared and visible spectral ranges (150 ns and 1064 nm, 10 ns and 1078 nm, 300 ps and 1078 nm, 220 ps and 539 nm, 100 fs and 800 nm.) are reported. The influence of the irradiation conditions (pulse duration, wavelength, laser intensity and the number of laser shots) on the structure and thickness of the laser-induced graphitized layer has been investigated. The effects of heat dissipation on the annealing duration and on the graphitized layer thickness are discussed for the case of laser processing with short pulses. It was found that the resulting morphology of the irradiated a-C:H film surface was determined by the concurrence of three processes: change of the mass density induced by structural transformations, multiple spallations of thin layers, and material evaporation. The laser-induced spallation is asserted to be the main factor limiting the laser microprocessing reproducibility for the examined a-C:H film; its effects were found to increase dramatically for longer (150 ns) laser pulses. The ablation (evaporation) rates of the a-C:H films and glassy carbon were revealed to be similar for femtosecond and picosecond pulses, but they essentially differed for nanosecond pulses. The ablation process demonstrated the same main features for both materials: (i) increase of the ablation rate with the pulse duration, and (ii) saturation of the ablation rate with fluence for picosecond and nanosecond pulses.     

Surface acoustic waves in diamond-like carbon films on LiNbO3

Diamond-like carbon (DLC) films have been reliably deposited on YZ LiNbO_3, and surface acoustic wave (SAW) velocity change has been observed. These relatively thin films increase the SAW velocity sufficiently, and they can be used for SAW devices. The cut-off behavior was observed at approximately 538 MHz in a 2-μm-thick DLC film on the LiNbO₃ substrate.     

Stresses in diamond-like carbon films

Internal stresses have been measured in diamond-like carbon (DLC) films deposited by d.c. plasma assisted chemical vapor deposition from methane, acetylene, or cyclohexane, and in nitrogen containing DLC films deposited from acetylene, or cyclohexane and nitrogen. The total hydrogen content in the films and the fraction of bound hydrogen have been analyzed by forward recoil elastic scattering and Fourier transform infrared spectroscopy respectively. It was found that in pure DLC films the stresses increase with increasing fraction of unbound hydrogen. The highest compressive stresses were obtained in the films deposited from methane and the lowest stresses in films deposited from cyclohexane. In the nitrogen containing DLC films the stresses decrease with increasing nitrogen content in the films. Stresses as low as 0.22 GPa were obtained in the films deposited from cyclohexane and nitrogen at a ratio of 1/15 in the plasma.     

Lubrication performance of diamond-like carbon and fluorinated diamond-like carbon coatings for intravascular guidewires

Diamond-like carbon (DLC) and fluorinated DLC (F-DLC) films were deposited on SUS316L guidewires using radio frequency (RF) plasma enhanced chemical vapor deposition (CVD), and the lubrication performance of DLC- or F-DLC-coated guidewires was then evaluated under in vitro conditions using a novel friction simulator developed for this study. Scanning electron microscopy (SEM) demonstrated that DLC or F-DLC film completely coated the specimens (SUS316L guidewires) and that polishing scars were substantially reduced. In the torturous vessel model, DLC- or F-DLC-coated guidewires exhibited significantly improved lubrication performance (by approximately 30% over that of uncoated wires). DLC and F-DLC films are thus promising candidates for lubricious coating of intravascular guidewires.     

Novel carbazole/pyridine-based host material for solution-processed blue phosphorescent organic light-emitting devices

3,6-Bis(3,5-di(pyridin-3-yl)phenyl)-9-phenyl-9H-carbazole, a novel host material for solution-processed blue phosphorescent organic light-emitting devices was synthesized by a Suzuki coupling reaction. The optical, electrochemical and thermal properties of this novel crabazole have been characterized. The compound exhibits a high glass-transition temperature (Tg = 161 °C) and high triplet energy (E_T = 2.76 eV). Additionally, atomic force microscopy measurements indicate that high-quality amorphous films of this novel compound can be prepared by spin-coating. Solution-processed blue phosphorescent organic light-emitting devices were obtained using the carbazole as the host material for the phosphorescence emitter iridium(III) bis(4,6-difluorophenylpyridinato)- picolinate and their electroluminescence properties were evaluated.