Krisztian Kordas

Chip cooling with integrated carbon nanotube microfin architectures

Efficient cooling of silicon chips using microfin structures made of aligned multiwalled carbon nanotube arrays is achieved. The tiny cooling elements mounted on the back side of the chips enable power dissipation from the heated chips on the level of modern electronics demands. The nanotube fins are mechanically superior compared to other materials being ten times lighter, flexible, and stiff at the same time. These properties accompanied with the relative simplicity of the fabrication makes the nanotube structures strong candidates for future on-chip thermal management applications.

Low-temperature large-scale synthesis and electrical testing of ultralong copper nanowires.

Copper nanowires (NWs) with uniform diameters and lengths ranging from several hundreds of nanometers to several micrometers have been prepared with high yield by a simple hydrothermal procedure. The X-ray diffraction (XRD) and energy dispersive X-ray spectroscopy (EDS) analysis data indicate that the copper nanowires are free of any contamination, while the electron diffraction (ED) analysis has revealed the nanowires to be single crystals. The nanowire growth mechanism has also been discussed. Hexadecylamine is the surface stabilizing agent in our method, while glucose facilitates formation of single-crystalline seeds on which the copper nanowires grow. The electrical properties of the as-synthesized copper NWs have also been investigated.

Nitrogen-Doped Anatase Nanofibers Decorated with Noble Metal Nanoparticles for Photocatalytic Production of Hydrogen

We report the synthesis of N-doped TiO(2) nanofibers and high photocatalytic efficiency in generating hydrogen from ethanol-water mixtures under UV-A and UV-B irradiation. Titanate nanofibers synthesized by hydrothermal method are annealed in air and/or ammonia to achieve N-doped anatase fibers. Depending on the synthesis route, either interstitial N atoms or new N-Ti bonds appear in the lattice, resulting in slight lattice expansion as shown by XPS and HR-TEM analysis, respectively. These nanofibers were then used as support for Pd and Pt nanoparticles deposited with wet impregnation followed by calcination and reduction. In the hydrogen generation tests, the N-doped samples were clearly outperforming their undoped counterparts, showing remarkable efficiency not only under UV-B but also with UV-A illumination. When 100 mg of catalyst (N-doped TiO(2) nanofiber decorated with Pt nanoparticles) was applied to 1 L of water-ethanol mixture, the H(2) evolution rates were as high as 700 μmol/h (UV-A) and 2250 μmol/h (UV-B) corresponding to photo energy conversion percentages of ∼3.6 and ∼12.3%, respectively.

Thermal oxidation of porous silicon: Study on structure

The structural changes of porous silicon (PS) samples during oxidation are investigated and analyzed using various microscopy techniques and x-ray diffraction. It is found that the surface roughness of oxidized PS layers increases with the oxidation at 200–400°C and decreased at 600–800°C. At 800°C a partially fused surface is observed. The oxide formed on the wall of porous silicon skeleton is amorphous. The shifts of Si(400) peaks are observed in the x-ray diffraction patterns, which are correlated to the lattice deformation induced by thermal expansion coefficient mismatch between the grown SiO2 and the residual Si, and to the intrinsic stress caused by the Si–O bonds at the Si–SiO2 interface. These explanations are supported by thermomechanical modeling using three-dimensional finite element method.

Three-Dimensional Carbon Nanotube Scaffolds as Particulate Filters and Catalyst Support Membranes

Three-dimensional carbon nanotube scaffolds created using micromachined Si/SiO2 templates are used as nanoparticulate filters and support membranes for gas-phase heterogeneous catalysis. The filtering efficiency of better than 99% is shown for the scaffolds in filtering submicrometer particles from air. In the hydrogenation of propene to propane reaction low activation energy of E(a) approximately 27.8 +/- 0.6 kJ x mol(-1), a considerably high turnover rate of approximately 1.1 molecules x Pd site(-1) x s(-1) and durable activity for the reaction are observed with Pd decorated membranes. It is demonstrated that appropriate engineering of macroscopic-ordered nanotube architectures can lead to multifunctional applications.

Electrical Transport and Field-Effect Transistors Using Inkjet-Printed SWCNT Films Having Different Functional Side Groups

The electrical properties of random networks of single-wall carbon nanotubes (SWNTs) obtained by inkjet printing are studied. Water-based stable inks of functionalized SWNTs (carboxylic acid, amide, poly(ethylene glycol), and polyaminobenzene sulfonic acid) were prepared and applied to inkjet deposit microscopic patterns of nanotube films on lithographically defined silicon chips with a back-side gate arrangement. Source-drain transfer characteristics and gate-effect measurements confirm the important role of the chemical functional groups in the electrical behavior of carbon nanotube networks. Considerable nonlinear transport in conjunction with a high channel current on/off ratio of approximately 70 was observed with poly(ethylene glycol)-functionalized nanotubes. The positive temperature coefficient of channel resistance shows the nonmetallic behavior of the inkjet-printed films. Other inkjet-printed field-effect transistors using carboxyl-functionalized nanotubes as source, drain, and gate electrodes, poly(ethylene glycol)-functionalized nanotubes as the channel, and poly(ethylene glycol) as the gate dielectric were also tested and characterized.

Laser-assisted metal deposition from liquid-phase precursors on polymers

Abstract In this work, a short review is presented for results utilizing the technique of laser-assisted metallization of dielectrics. Experimental efforts and results related to the metal (palladium (Pd), copper (Cu) and silver (Ag)) deposition on polymeric materials (polyimide (PI), mylar) are reported. These polymers and metals are chosen due to their growing importance in the rapidly-developing microelectronics packaging industry. The method of laser-induced chemical liquid-phase deposition (LCLD) offers many advantages compared to other techniques such as laser-induced forward transfer (LIFT), pulsed-laser deposition (PLD) and laser-assisted chemical vapor-phase deposition (LCVD). The LCLD is time and cost effective because vacuum tools and special pre-treatments are not required. The consumed chemicals used in precursors are non-harmful and easy to handle due to the liquid phase. For the optimal physical and chemical properties of deposits, the laser and solution parameters are varied. XeCl and KrF excimer and Ar + lasers are employed for executing the palladium, Ag and/or Cu formation on the polymer substrates. Chemical and physical analyses of the formed metal patterns are performed by EDX, XRD, FESEM, SEM, resistance and adhesion measurements.

Field Emission with Ultralow Turn On Voltage from Metal Decorated Carbon Nanotubes

A simple and scalable method of decorating 3D-carbon nanotube (CNT) forest with metal particles has been developed. The results observed in aluminum (Al) decorated CNTs and copper (Cu) decorated CNTs on silicon (Si) and Inconel are compared with undecorated samples. A significant improvement in the field emission characteristics of the cold cathode was observed with ultralow turn on voltage (Eto ∼ 0.1 V/μm) due to decoration of CNTs with metal nanoparticles. Contact resistance between the CNTs and the substrate has also been reduced to a large extent, allowing us to get stable emission for longer duration without any current degradation, thereby providing a possibility of their use in vacuum microelectronic devices.

Laser direct writing of copper on polyimide surfaces from solution

Conductive copper patterns were deposited on polyimide (PI) substrates by using a focused, scanned continuous wave (cw) Ar+ laser beam at 488 nm wavelength. The deposition process was initiated by a photothermal reaction of a tartarate-complex solution of Cu2+ ions in an alkaline and reducing environment. Deposits were characterised by Field Emission Scanning Electron Microscope (FESEM), Energy Dispersive X-ray (EDX) Spectrometry, DEKTAK profilometer and resistance measurements. The dependence of the characteristics of laser direct written patterns on the scanning speed of the laser beam, number of scans and laser power was examined. Uniform copper lines covered with copper-oxide (line width from 30 to 60 μm and height from 2 to 20 μm) with high conductivity and adhesion were achieved under optimised conditions.

“Double‐Peak” Catalytic Activity of Nanosized Gold Supported on Titania in Gas‐Phase Selective Oxidation of Ethanol

Recent years have seen a growing amount of fundamental research dealing with selective oxidation of alcohols and polyols using molecular oxygen (air) as a cheap and clean oxidant in the presence of solid catalysts. In this respect, supported gold nanoparticles have attracted great attention owing to their unique catalytic properties under mild conditions. Moreover, gold catalysts are becoming increasingly important for the conversion of biomass-derived alcohols, such as ethanol and glycerol, into other useful chemicals. Bioethanol, in particular, is an example of a promising renewable feedstock to obtain corresponding products of oxidation and concurrent reactions; acetaldehyde, 1,1-diethoxyethane, ethyl acetate and acetic acid, which are normally formed one by one with increase of temperature. As a result, more or less complex mixtures of these products or a predominant individual product can be obtained depending on the reaction conditions and the nature of the catalyst (gold particle size, support, preparation procedure). Notably, exactly the same spectrum of products, for example, aldehydes, acetals, esters and carboxylic acids, is typically produced in the presence of other supported metals (e.g. , Pt, Pd, Ru) or metal oxide catalysts (e.g. , V2O5, NbMoVOx), although generally under harsher conditions. Therefore, it seems quite possible that all reactions indicated above have similar mechanistic aspects. However, no generally accepted mechanism has, to date, been formulated for these reactions (see, however, Refs. [8–11]), as it has been for gold-catalyzed reactions of CO, O2, H2, and other small molecules. [12–13] During our monitoring of a gas-phase oxidation of ethanol, a large variety of solid catalysts, such as supported noble metals, metal oxides, and multicomponent systems have been tested. Among them, about thirty different supported gold catalysts were examined. Herein we report an unusual catalytic behavior of Au/TiO2, which was the only tested catalyst to give rise to a second low-temperature peak of activity. The most active gold catalysts are known to be those that contain small particles of gold (<10 nm in diameter), especially on reducible supports such as titania or ceria. 14] Taking this into account, several samples of 2 wt % Au/TiO2 were prepared according to a direct ion-exchange procedure 15] using ammonia as a washing agent to give an average gold particles size close to 2 nm (Figure 1; see also the Supporting Information). The catalytic performance of Au/TiO2 (d = 1.9 1 nm) sample