Electronic module assembly

Electronics is the vital basis for innovations and the essential enabler for global trends like connectivity, electro mobility and renewable energies. These applications require high performance and reliability of the electronic modules. Their assembly combines very heterogeneous process chains like remarkable productive and diminutive surface mount technology (SMT), powerful and robust power electronic interconnection techniques, as well as pioneering reel-to-reel based organic electronic printing. After briefly outlining the enormous global economic impact of electronic modules, this paper presents the state of the art of electronic module assembly including substrate materials, electronic components, packaging and assembly processes as well as quality and reliability testing methods.     

Spatiotemporal Magnetocaloric Microenvironment for Guiding the Fate of Biodegradable Polymer Implants

The degradation behavior of implants is significantly important for bone repair. However, it is still unprocurable to spatiotemporally regulate the degradation of the implants to match bone ingrowth. In this paper, a magneto-controlled biodegradation model is established to explore the degradation behavior of magnetic scaffolds in a magnetothermal microenvironment generated by an alternating magnetic field (AMF). The results demonstrate that the scaffolds can be heated by magnetic nanoparticles (NPs) under AMF, which dramatically accelerated scaffold degradation. Especially, magnetic NPs modified by oleic acid with a better interface compatibility exhibit a greater heating efficiency to further facilitate the degradation. Furthermore, the molecular dynamics simulations reveal that the enhanced motion correlation between magnetic NPs and polymer matrix can accelerate the energy transfer. As a proof-of-concept, the feasibility of magneto-controlled degradation for implants is demonstrated, and an optimizing strategy for better heating efficiency of nanomaterials is provided, which may have great instructive significance for clinical medicine.     

Synthesis and characterization of Ce/SiOC nanocomposites through the polymer derived ceramic method and evaluation of their catalytic activity

Cerium oxide and silicon oxycarbide (Ce/SiOC) porous nanocomposites have been synthesized through the polymer derived ceramic route. In the synthesis of the preceramic precursors, the addition of urea facilitates the deposition of Cerium atoms on the surface of SiO₂ nanoparticles since it prevents the SiO₂ from agglomeration. Both Ce and urea affects the structural and textural parameters of the obtained ceramics. Less crosslinked structures are formed when the urea concentration increases and it also provokes a reduction of the carbon crystallite size. Cerium, on the other hand, induces an increase of the carbon size as well as the number of SiOC units. Pore anisotropy and smoothness of the surface are also dependent on the composition of the material. As expected, the better thermocatalytic behavior against CO₂ decomposition is found at the largest Ce amounts but also, smooth surfaces and low pore anisotropies favor the accessibility of the gases to the thermocatalytic centers.     

Effects of SO2 on selective catalytic reduction of NO with NH3 over a TiO2 photocatalyst

The effect of SO₂ gas was investigated on the activity of the photo-assisted selective catalytic reduction of nitrogen monoxide (NO) with ammonia (NH₃) over a TiO₂ photocatalyst in the presence of excess oxygen (photo-SCR). The introduction of SO₂ (300 ppm) greatly decreased the activity of the photo-SCR at 373 K. The increment of the reaction temperature enhanced the resistance to SO₂ gas, and at 553 K the conversion of NO was stable for at least 300 min of the reaction. X-ray diffraction, FTIR spectroscopy, thermogravimetry and differential thermal analysis, x-ray photoelectron spectroscopy (XPS), elemental analysis and N₂ adsorption measurement revealed that the ammonium sulfate species were generated after the reaction. There was a strong negative correlation between the deposition amount of the ammonium sulfate species and the specific surface area. Based on the above relationship, we concluded that the deposition of the ammonium sulfate species decreased the specific surface area by plugging the pore structure of the catalyst, and the decrease of the specific surface area resulted in the deactivation of the catalyst.     

Improved optical and structural properties of cadmium sulfide nanostructures for optoelectronic applications

In this study, the effect of ZnO seed layer on the growth of uniform CdS nanostructures was investigated using chemical bath deposition technique. Besides, the influence of molar concentration of reagents on the surface morphology, structural and optoelectrical properties of the deposited CdS thin films were examined. The CdS nanostructures were grown on bare glass and ZnO/glass substrates with different reagent molar concentrations. The results indicated an improvement in the homogeneity and uniformity of the grown CdS nanostructures on ZnO seed layer which can be due to the low lattice mismatch between ZnO and CdS structures. The CdS/ZnO samples were optimized by changing the molar concentration of reagents. A three–dimensional intersecting vertical nanosheet morphology with hexagonal structure was obtained when modified chemical concentration of 0.5 M was applied. The XRD pattern of CdS nanosheets indicated the hexagonal phase of CdS which were strongly orientated along (002) plane. The elevated intensity of dominant peak related to this sample confirmed the improved crystal quality of this CdS nanostructure comparing to the other samples. The UV–Vis spectrum demonstrated a high absorption coefficient for CdS intersecting nanosheets which might be due to the high specific surface area and light trapping behavior of this sample. The photoluminescence study also showed an improvement in optical properties of optimized CdS nanostructures. In order to study the optoelectrical properties of CdS nanostructures, metal–semiconductor–metal photodetectors were fabricated with different CdS samples and their current–voltage characteristics were analyzed. The results indicated an enhancement in photosensitivity, responsivity, and speed of photodetectors based on optimized CdS nanostructures.     

Cover Picture: UV‐Light‐Induced Swelling and Visible‐Light‐Induced Shrinking of a TiO2‐Containing Redox Gel (Adv. Mater. 9/2007)

Polyacrylate gels containing Ag⁺ and TiO₂ nanoparticles are shown to swell under UV light and shrink under visible light in water. In work reported by Tetsu Tatsuma and co‐workers on p. 1249, the TiO₂ absorbs UV light and reduces the Ag⁺, whereas the deposited Ag absorbs visible light and dissolves itself. These redox reactions change the interactions between the polymer chains and eventually the volume of the gel, as shown on the cover.     

Linear and non-linear conductive spectra of polyethylene oxide/salt complex

A new experimental system has been developed, which enables measurements of linear as well as non-linear complex conductivities to be made. The frequency dependence of linear to fifth-order non-linear complex conductivities at different temperatures in a polyethylene oxide/salt complex can then be measured. A characteristic conduction relaxation phenomenon was observed in the spectra, which suggested the existence of different ion-conduction mechanisms between the high- and low-frequency regions. It was also found that the ratio of linear to non-linear conductivities was closely related to the elementary process of ionic transport. Furthermore, this ratio obtained from non-linear measurements allowed an estimate of the important parameters which characterized ionic transport in ion-conducting polymers, such as the hopping distance of an ion or the size of a connected cluster of the site capable of ion hopping, without the need for any additional assumptions. Thus, it was found that in a polyethylene oxide/salt complex, the typical size of a connected cluster of the effective sites capable of ion hopping was approximately 4 nm.     

An updated correlation for crack-arrest fracture toughness for nuclear reactor pressure vessel steels

An updated and statistically-rigorous correlation is provided for crack-arrest toughness values versus normalized temperature for light-water nuclear reactor pressure vessel (RPV) steels. The database used in this effort is larger than applied heretofore and includes results from tests of laboratory-size specimens and from tests of large-scale specimens, which contain features prototypical of operating RPVs. The mathematical methodology used is based on a lognormal distribution, with its parameters calculated by orthogonal distance regression. This correlation was developed as one of several items updated for use in the US Nuclear Regulatory Commission's extensive program to evaluate and potentially revise its rule for ensuring structural integrity of operating RPVs when subjected to pressurized thermal-shock transients.     

Tight upper bound on the number of edges in a bipartite K3,3-free or K5-free graph with an application

We show that an n-vertex bipartite K_3,3-free graph with n?3 has at most 2n−4 edges and that an n-vertex bipartite K₅-free graph with n?5 has at most 3n−9 edges. These bounds are also tight. We then use the bound on the number of edges in a K_3,3-free graph to extend two known NC algorithms for planar graphs to K_3,3-free graphs.     

Hot carrier magnetophonon spectroscopy of semiconductors in high magnetic fields up to 40 T

Hot carrier magnetophonon resonances of n-type Si, short channel InP and p-type InSb were investigated in pulsed high magnetic fields up to 40 T. Using a recently developed high resolution technique in pulsed high fields, many new features of the hot carrier-phonon interactions in high magnetic fields were found.