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With the best overall electronic and thermal properties, single crystal diamond (SCD) is the extreme wide bandgap material that is expected to revolutionize power electronics and radio-frequency electronics in the future. However, turning SCD into useful semiconductors requires overcoming doping challenges, as conventional substitutional doping techniques, such as thermal diffusion and ion implantation, are not easily applicable to SCD. Here we report a simple and easily accessible doping strategy demonstrating that electrically activated, substitutional doping in SCD without inducing graphitization transition or lattice damage can be readily realized with thermal diffusion at relatively low temperatures by using heavily doped Si nanomembranes as a unique dopant carrying medium. Atomistic simulations elucidate a vacancy exchange boron doping mechanism that occurs at the bonded interface between Si and diamond. We further demonstrate selectively doped high voltage diodes and halfwave rectifier circuits using such doped SCD. Our new doping strategy has established a reachable path toward using SCDs for future high voltage power conversion systems and for other novel diamond based electronic devices. The novel doping mechanism may find its critical use in other wide bandgap semiconductors. [ABSTRACT FROM AUTHOR]

This paper presents the experimental behavior of low-energy impact and quasi-static compression test of shifted-tri-axial structural wood-fiber-based composite panels made from laminated paper. The experimental results were analyzed based on design parameters and configurations of panels for the further design and optimization. The results showed that the face stiffness and strength was a significant factor to improve both impact performance and compressive performance. The panels made with additional carbon fiber fabric composite faces had higher energy absorption compared with the same panels made without it. The core configuration also affected the impact behavior of the panels, the foam filled core integrated with the shifted-tri-axial rib structure improved the impact load and absorbed more energy than the same panels without the foam. Further, the structure and size of the element in the core influenced the impact performance and energy absorption. The location for both compression and impact at the triangular lattice element center of the ribs had higher absorbed energy than the location at the hexagonal lattice element center of the ribs. A 3D contour surface map of maximum energy absorption was made based on the experimental data, the contour shows localized energy absorption based on the impact location on the core, the small triangular lattice element of the core had highest maximum energy absorption of panels. For both the quasi-static compression tests and the low-velocity impact tests, the panels with the same core configuration had similar compressive load-displacement trends during the early contact phase. However, the peak load was higher in compression than the peak load for the low-velocity impact for panels with the same configuration. [ABSTRACT FROM AUTHOR]

Digital image sensors in hemispherical geometries offer unique imaging advantages over their planar counterparts, such as wide field of view and low aberrations. Deforming miniature semiconductor-based sensors with high-spatial resolution into such format is challenging. Here we report a simple origami approach for fabricating single-crystalline silicon-based focal plane arrays and artificial compound eyes that have hemisphere-like structures. Convex isogonal polyhedral concepts allow certain combinations of polygons to fold into spherical formats. Using each polygon block as a sensor pixel, the silicon-based devices are shaped into maps of truncated icosahedron and fabricated on flexible sheets and further folded either into a concave or convex hemisphere. These two electronic eye prototypes represent simple and low-cost methods as well as flexible optimization parameters in terms of pixel density and design. Results demonstrated in this work combined with miniature size and simplicity of the design establish practical technology for integration with conventional electronic devices. [ABSTRACT FROM AUTHOR]

Photo detection of ultraviolet (UV) light remains a challenge since the penetration depth of UV light is limited to the nanometer scale. Therefore, the doping profile and electric field in the top nanometer range of the photo detection devices become critical. Traditional UV photodetectors usually use a constant doping profile near the semiconductor surface, resulting in a negligible electric field, which limits the photo-generated carrier collection efficiency of the photodetector. Here, we demonstrate, via the use of an optimized gradient boron doping technique, that the carrier collection efficiency and photo responsivity under the UV wavelength region have been enhanced. Furthermore, the ultrathin p+-i-n junction shows an avalanche gain of 2800 and an ultra-low junction capacitance (sub pico-farad), indicating potential applications in the low timing jitter single photon detection area. [ABSTRACT FROM AUTHOR]

This paper presents experimental results of both quasi-static compression and low-velocity impact behavior for tri-axial bio-composite structural panels using a spherical load head. Panels were made having different core and face configurations. The results showed that panels made having either carbon fiber fabric composite faces or a foam-filled core had significantly improved impact and compressive performance over panels without either. Different localized impact responses were observed based on the location of the compression or impact relative to the tri-axial structural core; the core with a smaller structural element had better impact performance. Furthermore, during the early contact phase for both quasi-static compression and low-velocity impact tests, the panels with the same configuration had similar load-displacement responses. The experimental results show basic compression data could be used for the future design and optimization of tri-axial bio-composite structural panels for potential impact applications. [ABSTRACT FROM AUTHOR]

The static and fatigue bending behavior of wood-fiber-based tri-axial engineered sandwich composite panels (ESCP) has been investigated by four-point bending tests. Fatigue panels and weakened panels (wESCP) with an initial interface defect were manufactured for the fatigue tests. Stress s vs. number of cycles curves (S-N) were recorded under the different stress levels. The primary failure mode in the fatigue tests was observed in the shear zone (epoxy debonding), which was different from face failure in the pure bending zone for the static bending test. For residual bending (RB) test, epoxy debonding failure occurred between the pure bending zone and shear zone. Macro cracks along the core/face interface developed as the number of cycles increased during the fatigue life. The crack propagation or damage for the panels submitted to fatigue test can be described as a three-stage damage process of first non-linear portion, followed by linear damage accumulation, and lastly nonlinear accelerated damage. Bending stiffness degradation at the higher load level had faster degradation during fatigue life. The dissipated energy of the panels was small due to the high stiffness of the materials. [ABSTRACT FROM AUTHOR]

Wafer-scale strained bilayer graphene is demonstrated by employing a silicon nitride (Si3N4) stressor layer. Different magnitudes of compressive stress up to 840 MPa were engineered by adjusting the Si3N4 deposition recipes, and different strain conditions were analyzed using Raman spectroscopy. The strained graphene displayed significant G peak shifts and G peak splitting with 16.2 cm–1 and 23.0 cm–1 of the G band and two-dimensional band shift, which corresponds to 0.26% of strain. Raman mapping of large regions of the graphene films found that the largest shifts/splitting occurred near the bilayer regions of the graphene films. The significance of our approach lies in the fact that it can be performed in a conventional microfabrication process, i.e., the plasma enhanced chemical vapor deposition system, and thus easily implemented for large scale production. [ABSTRACT FROM AUTHOR]

In this paper, we demonstrate microwave flexible thin-film transistors (TFTs) on biodegradable substrates towards potential green portable devices. The combination of cellulose nanofibrillated fiber (CNF) substrate, which is a biobased and biodegradable platform, with transferrable single crystalline Si nanomembrane (Si NM), enables the realization of truly biodegradable, flexible, and high performance devices. Double-gate flexible Si NM TFTs built on a CNF substrate have shown an electron mobility of 160 cm²/Vs and fT and fmax of 4.9GHz and 10.6 GHz, respectively. This demonstration proves the microwave frequency capability and, considering today's wide spread use of wireless devices, thus indicates the much wider utility of CNF substrates than that has been demonstrated before. The demonstration may also pave the way toward portable green devices that would generate less persistent waste and save more valuable resources. [ABSTRACT FROM AUTHOR]

In this paper, we demonstrate microwave flexible thin-film transistors (TFTs) on biodegradable substrates towards potential green portable devices. The combination of cellulose nanofibrillated fiber (CNF) substrate, which is a biobased and biodegradable platform, with transferrable single crystalline Si nanomembrane (Si NM), enables the realization of truly biodegradable, flexible, and high performance devices. Double-gate flexible Si NM TFTs built on a CNF substrate have shown an electron mobility of 160 cm²/V.s and fT and fmax of 4.9GHz and 10.6 GHz, respectively. This demonstration proves the microwave frequency capability and, considering today's wide spread use of wireless devices, thus indicates the much wider utility of CNF substrates than that has been demonstrated before. The demonstration may also pave the way toward portable green devices that would generate less persistent waste and save more valuable resources. [ABSTRACT FROM AUTHOR]

A method of creating tunable and programmable biaxial compressive strain in silicon nanomembranes (Si NMs) transferred onto a Kapton® HN polyimide film has been demonstrated. The programmable biaxial compressive strain (up to 0.54%) was generated utilizing a unique thermal property exhibited by the Kapton HN film, namely, it shrinks from its original size when exposed to elevated temperatures. The correlation between the strain and the annealing temperature was carefully investigated using Raman spectroscopy and high resolution X-ray diffraction. It was found that various amounts of compressive strains can be obtained by controlling the thermal annealing temperatures. In addition, a numerical model was used to evaluate the strain distribution in the Si NM. This technique provides a viable approach to forming in-plane compressive strain in NMs and offers a practical platform for further studies in strain engineering. [ABSTRACT FROM AUTHOR]

A graphene transistor with a bottom-gate coplanar structure and an atomic layer deposition (ALD) aluminum oxide (Al2O3) gate dielectric is demonstrated. Wetting properties of ALD Al2O3 under different deposition conditions are investigated by measuring the surface contact angle. It is observed that the relatively hydrophobic surface is suitable for adhesion between graphene and ALD Al2O3. To achieve hydrophobic surface of ALD Al2O3, a methyl group (CH3)-terminated deposition method has been developed and compared with a hydroxyl group (OH)-terminated deposition. Based on this approach, bottom-gate coplanar graphene field-effect transistors are fabricated and characterized. A post-thermal annealing process improves the performance of the transistors by enhancing the contacts between the source/drain metal and graphene. The fabricated transistor shows an Ion/Ioff ratio, maximum transconductance, and field-effect mobility of 4.04, 20.1 μS at VD = 0.1 V, and 249.5 cm²/V·s, respectively. [ABSTRACT FROM AUTHOR]

Mechanical analysis is presented for new high-strength sandwich panels made from wood-based phenolic impregnated laminated paper assembled with an interlocking tri-axial ribbed core. Four different panel configurations were tested, including panels with fiberglass fabric bonded to both outside faces with self-expanding urethane foam used to fill the ribbed core. The mechanical behaviors of the sandwich panels were strength tested via flatwise compression, edgewise compression, and third-point load bending. Panels with fiberglass exhibited significantly increased strength and apparent MOE in edgewise compression and bending, but there were no noticeable effects in flatwise compression. The foam provided improved support that resisted both rib buckling and face buckling for both compression and bending tests. Post-failure observation indicated that core buckling dominated the failures for all configurations used. It is believed that using stiffer foam or optimizing the dimension of the core might further improve the mechanical performance of wood-based sandwich panels. [ABSTRACT FROM AUTHOR]

Poly(ethylene terephthalate) (PET) resin is one of the most widely used thermoplastics, especially in packaging. Because thermal and hydrolytic degradations, recycled PET (RPET) exhibits poor mechanical properties and lacks moldability. The effects of adding elastomeric modifiers, chain extenders (CE), and poly(butylene adipate- co-terephthalate), PBAT, as a toughener to RPET on its moldability and mechanical property were investigated. Melt blending of RPET with CE, thermoplastic elastomer (TPE), and/or PBAT was performed in a thermokinetic mixer (K-mixer). The blended materials were then injection molded to produce tensile specimens. Various techniques were used to study the mechanical properties, rheological properties, compatibility, and crystallization behavior of the RPET blends. By melt blending with proper additives, recycled PET regained its moldability, thereby enabling the recycling of RPET. Furthermore, the addition of CE greatly enhanced the mechanical properties of RPET. While the RPET and TPE blends also showed improved mechanical properties, the improvement was less significant and the blends were often immiscible due to the difference in polarities between RPET and TPE. Finally, it was found that the mechanical properties of RPET blends depended on the prior thermal history of the material and could be improved with an extra annealing step that increased the degree of crystallinity. POLYM. ENG. SCI., 2011. © 2011 Society of Plastics Engineers [ABSTRACT FROM AUTHOR]

The article presents a study on the chemical and mechanical characteristics of the mixture of poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) and poly(butylene adipate-co-terephthalate) (PBAT). The study, which used three different weight ratios prepared via conventional and microcellular injection molding process, revealed better miscibility for solid specimens compared to its microcellular counterpart. It was also found that the PHBV cystallinity decreased with an increasing PBAT content for both solid and microcellular samples.

Water-soluble, doxorubicin (DOX) conjugated gold nanoparticles (DOX conjugated Au NPs) exhibiting a significant pH-responsive drug release profile have been prepared and characterized in this study. The Au NPs were stabilized by thiolated methoxy polyethylene glycol (MPEG-SH) and methyl thioglycolate (MTG) at an equal molar ratio. The anticancer drug DOX was conjugated to the MTG segments of the thiol-stabilized Au NPs using hydrazine as the linker. The resulting hydrazone bonds formed between the DOX molecules and the MTG segments of the thiol-stabilized Au NPs are acid cleavable, thereby providing a strong pH-responsive drug release profile. The MPEG segments attached to the Au NPs provide the Au NPs with excellent solubility and stability in an aqueous medium while potentially enhancing the circulation time. The DOX loading level was determined to be 23 wt.%. The DOX release rate from the DOX conjugated Au NPs in an acid medium (i.e., pH 5.3) was dramatically higher than that in physiological conditions (i.e., pH 7.4). The DOX conjugated Au NPs and/or the DOX released from them were found both at the perinuclear regions and the nuclei of 4T1 tumor cells after incubation in a DOX conjugated Au NPs solution for 28 h. These novel DOX conjugated Au NPs have the potential to simultaneously enhance CT imaging contrast and facilitate photothermal cancer therapy while delivering anticancer drugs to their target sites. [ABSTRACT FROM AUTHOR]

The article examines the material properties of biobased and biodegradable polylactide (PLA)-pine wood flour (PWF) composites, prepared using a kinetic-mixer and an injection molding machine. According to the authors, the PWF composites treated with silane exhibited higher storage modulus than those without the silane treatment and the degree of crystallinity of the PLA-PWF composites increased significantly with the PWF content. The authors also add that PWF with silane had a positive effect on its nucleating ability.

New amphiphilic polymer networks were synthesized by the free‐radical copolymerization of α,ω‐diacryl polycaprolactone (DAPCL) and N‐vinylpyrrolidone (NVP), which was initiated by 0.5% azobisisobutyronitrile at 70°C. The chemical structures of the networks were characterized by proton nuclear magnetic resonance spectrometry. The NVP/DAPCL feed ratio played an important role in the crosslinking process. The synthesized amphiphilic polymer networks exhibited controlled swelling properties in water and organic solvents (ethanol, acetones, and toluene). A porous structure was observed for the amphiphilic polymer networks under a scanning electron microscope. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007 [ABSTRACT FROM AUTHOR]

This article presents the development and characterization of transparent poly(styrene‐r‐maleic anhydride) (SMA)/alumina nanocomposites for potential use in optical applications. Chemically treated spherical alumina nanoparticles were dispersed in an SMA matrix polymer via the solution and melt‐compounding methods to produce 2 wt % nanocomposites. Field emission scanning electron microscopy was used to examine the nanoparticle dispersion. When the solution method was used, nanoparticle reagglomeration occurred, despite the fairly good polymer wetting. However, through the coating of the alumina nanoparticles with a thin layer (ca. 20 nm) of low‐molecular‐weight SMA, reagglomeration was absent in the melt‐compounded samples, and this resulted in excellent nanoparticle dispersion. The resultant nanocomposites were semitransparent to visible light at a 2‐mm thickness with improved UV‐barrier properties. Their impact strengths, tensile strengths, and strains at break were slightly reduced compared with those of their neat resin counterpart, whereas a small enhancement in their moduli was achieved. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007 [ABSTRACT FROM AUTHOR]

The article investigates the possibility of formulating high performance polylactic acid (PLA) composites using rubber and nanoclay simultaneously. Identification of the appropriate types of core-shell rubber and nanoclay for PLA separately was first conducted. The effects of adding core-shell rubber and nanoclay on the mechanical and thermal properties of PLA were then examined.

Studies the effects of submicron core-shell rubber (CSR) particles, nanoclay fillers, and molding parameters on the mechanical properties and cell structure of injection-molded microcellular polyamide-6 (PA6) composites. Comparison between experimental results of PA6 nanocomposites with 5.0 and 7.5 weight percent clay loadings and of CSR-modified PA6 composites with 0.5 and 3.1 weight percent CSR loadings; Effectiveness of the nanoclay in promoting a smaller cell size, larger cell density, and higher tensile strength for microcellular injection molding parts; Effect of a higher CSR loading on the process and on the properties of the parts.

The crystallization behaviors of polyamide-6 (PA-6) and its nanocomposites undergoing the microcellular injection molding process are studied using Transmission Electron Microscopy (TEM), X-ray Diffractometer (XRD), Polarized Optical Microscopy (POM), and Differential Scanning Calorimetry (DSC). The relationships among the morphology, the mechanical property of the molded parts, and the crystallization behavior are investigated. With the addition of nanoclays in microcellular injection molded parts, the growth of the α-form crystal is suppressed and the formation of γ-form crystals is promoted. Both nanoclay and dissolved gas have a big influence on PA-6 crystalline structures. The existence of nanoclay increases the initial crystallization rate. But with extra addition of nanoclays in the polymer matrix, the increase of crystallization rate is reduced. Microcellular injection molded nanocomposites with proper amount of nanoclays possess the maximum crystallization activation energy and produce a finer and denser microcell structure which leads to better mechanical properties. [ABSTRACT FROM AUTHOR]

This paper presents the effects of processing parameters and submicron core-shell rubber particle filler on the mechanical properties and cell morphology of microcellular injection molded polyamide-6 (PA-6) composites. Three types of materials are studied, namely, neat PA-6 resin, and 0.5 wt% and 3.1 wt% core-shell rubber polybutylacrylate-polymethylmethacrylate-filled PA-6 composites. This study shows that the addition of a small amount (0.5%) of core-shell rubber particles improved the ductility and impact strength of microcellular injection molded PA-6 samples. In comparison to the microcellular injection molded PA-6 polymer-clay nanocomposite, the samples with a small amount (0.5%) of core-shell rubber had much higher impact strength and ductility. The small addition of core-shell rubber also reduced cell size and increased cell density of the microcellular injection molded PA-6 parts, in comparison to their neat resin counterparts. On the other hand, at higher core-shell rubber loading, the cell size and density were found to be similar to that of the neat resin. [ABSTRACT FROM AUTHOR]

The effects of nanoclay addition into polyamide-6 (PA-6) neat resin and processing parameters on cell density and size in microcellular injection molded components are investigated. The analyses are performed on the sprue section of standard ASTM D 638-02 tensile bars molded based on a fractional four-factorial, three-level, L9 Taguchi design of experiments (DOE) with varying melt temperature, injection speed, super critical fluid (SCF) concentration, and shot size. It is found that the presence of nanoclay greatly reduced the cell size and increased the cell density when compared to neat resin processed under identical molding conditions. In addition, cell size distribution at the sprite center was, in general, the largest, gradually decreasing toward the skin for both the neat resin and the nanocomposite. Finally, in contrast to neat resin, in which shot size and injection speed were important to cell density and all molding parameters affected cell growth, the cell size and density for nanocomposite only depended strongly on shot size. [ABSTRACT FROM AUTHOR]

From large industrial computers to non-portable home appliances and finally to light-weight portable gadgets, the rapid evolution of electronics has facilitated our daily pursuits and increased our life comforts. However, these rapid advances have led to a significant decrease in the lifetime of consumer electronics. The serious environmental threat that comes from electronic waste not only involves materials like plastics and heavy metals, but also includes toxic materials like mercury, cadmium, arsenic, and lead, which can leak into the ground and contaminate the water we drink, the food we eat, and the animals that live around us. Furthermore, most electronics are comprised of non-renewable, non-biodegradable, and potentially toxic materials. Difficulties in recycling the increasing amount of electronic waste could eventually lead to permanent environmental pollution. As such, discarded electronics that can naturally degrade over time would reduce recycling challenges and minimize their threat to the environment. This review provides a snapshot of the current developments and challenges of green electronics at the semiconductor device level. It looks at the developments that have been made in an effort to help reduce the accumulation of electronic waste by utilizing unconventional, biodegradable materials as components. While many semiconductors are classified as non-biodegradable, a few biodegradable semiconducting materials exist and are used as electrical components. This review begins with a discussion of biodegradable materials for electronics, followed by designs and processes for the manufacturing of green electronics using different techniques and designs. In the later sections of the review, various examples of biodegradable electrical components, such as sensors, circuits, and batteries, that together can form a functional electronic device, are discussed and new applications using green electronics are reviewed. [ABSTRACT FROM AUTHOR]

Polycrystalline GeSn thin films on Si substrates with a Sn composition up to 4.5% have been fabricated and characterized. The crystalline structure, surface morphology, and infrared (IR) absorption coefficient of the annealed GeSn thin films were carefully investigated. It was found that the GeSn thin films with a Sn composition of 4.5% annealed at 450 °C possessed a desirable polycrystalline structure according to X-ray diffraction (XRD) analyses and Raman spectroscopy analyses. In addition, the absorption coefficient of the polycrystalline GeSn thin films in the IR region was significantly better than that of the single crystalline bulk Ge. [ABSTRACT FROM AUTHOR]