We have measured the pressure and temperature dependence of 57 Co diffusion in structurally relaxed Co 81 Zr 19 glass. The activation enthalpy and the preexponential factor are 1.4 eV and 8.4 3 10 29 m 2 s 21 . The pressure dependence is extremely small and yields an activation volume of V act ͑0.08 6 0, 1͒V, where V is the mean atomic volume. These results allow us to rule out that diffusion at this alloy composition is mediated by vacancylike thermal defects, as recently suggested for Zr-rich metal-metal glasses [A. Grandjean et al., Phys. Rev. Lett. 78, 697 (1997)]. The validity of the Keyes relationship is critically discussed. [S0031-9007(98)05821-9]
Bulk polytetrafluoroethylene (PTFE) possesses excellent chemical stability and dielectric properties. Indeed, thin films with these same characteristics would be ideal for electret applications. Previously, the electret properties of PTFE-like thin films produced by rf sputtering or plasma enhanced chemical vapor deposition were found to deteriorate due to structural changes and surface oxidation. In this article, the technique of initiated chemical vapor deposition (iCVD) is evaluated for electret applications for the first time. The iCVD method is known for its solvent-free deposition of conformal, pinhole-free polymer thin films in mild process conditions. It is shown that PTFE thin films prepared in this way, show excellent agreement to commercial bulk PTFE with regard to chemical properties and dielectric dissipation factors. After ion irradiation in a corona discharge the iCVD PTFE thin films exhibit stable electret properties, which can be tailored by the process parameters. Due to the mild deposition conditions, the iCVD technique is suitable for deposition on flexible organic substrates for the next-generation electret devices. It is also compatible with state-of-the-art microelectronic processing lines due to the characteristics of conformal growth and easy scaling up to larger size substrates.
In this work, we demonstrate the first synthesis of photochromic polymer thin films via initiated chemical vapor deposition (iCVD) using bifunctional, crystalline styrenediazocine as a photochromic unit. Since it represents a solid compound, an innovative custom-made sublimation unit is introduced, which allows the sublimation of the chromophore as well as its transport inside the reactor chamber, maintaining the functionality of the photoswitch. Styrenediazocine was co-polymerized with 1,3,5trivinyl-1,3,5-trimethylcyclotrisiloxane (V 3 D 3 ), a heterocycle with triple vinyl functionality, in a radical polymerization reaction from the gas phase. The structural as well as functional properties of the resulting films were characterized by various methods, including X-ray photoelectron spectroscopy (XPS), Fourier-transform infrared (FT-IR) spectroscopy, and UV−vis spectroscopy. It could be confirmed that, via iCVD, photoswitchable polymer thin films have been obtained. The polymer is based on a copolymer structure where all photoswitchable molecules are covalently bonded in the main polymer chain. Our approach could pave the way for a completely new class of high-quality, photochromic thin films that are basically applicable on almost every kind of substrate for novel, interdisciplinary application fields, where particularly classical wet chemistry methods cannot be applied.
A radio frequency (RF) hollow discharge configuration is presented, which makes use of a combination of RF plasma generation and the hollow cathode effect. The system was especially designed for the treatment of nanoparticles, plasma polymerization, and nanocomposite fabrication. The process gas streams through the plasma in the inner of the cylindrical electrode system. In the here presented measurements, pure argon and argon with oxygen admixtures are exemplarily used. The discharge is characterized by probe measurements in the effluent, electrical measurements of the discharge parameters, and visual observations of the plasma glow. It is found that the RF fluctuations of the plasma potential are weak. The plasma potential resembles the one of a DC hollow cathode discharge, the RF hollow electrode acts as a cathode due to the self-bias, and a high voltage sheath forms in its inner cylinder.
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