A specific type of buried defect in lamellar phase diblock copolymer was studied by experiments and simulations using self-consistent field theory (SCFT). The defects had 3-dimensional structures and created hexagonally arranged holes. They existed not only on the substrate with the guide structures but in fingerprints. The simulation results suggested that one of the causes of the defects is mismatch of the surface affinity of the neutral layer.

Since 2005 the West Houston Center for Science & Engineering (WHC) has provided opportunities for select cohorts of community college students to participate in summer research experiences. Participating research institutions include regional universities, NASA-JSC and Sandia National Laboratories (NM). Research activities cross numerous engineering, physical and biological sciences, and computational disciplines, and have been supported by federal agencies and corporate/educational foundations. These experiences have generated three important outcomes: (1) Providing significant motivation for students regarding university transfer and completion; (2) Generating realistic expectations for students regarding completion of their undergraduate degrees, and transitioning into the science and engineering workforce and/or graduate school; and, (3) Providing support for the creation of a formal materials science educational program at the West Houston Center. This paper describes the influence and impact that the Materials Research Society, through its members, conferences, and working committees, has contributed to the transition of the West Houston Center as it moves from a broad based science and engineering educational center to one with a concentration on materials science.

Field effect transistors with graphene channels were interfaced with arrays of semiconductor quantum dots (QD). The electrical characteristics of the elements were assessed. The channel response to white light illumination was also assessed as a function of drain-source and gate-source biases.

The effect of low energy implantation of P or C ions in 3C-SiC on the properties of Ti/Ni/Au contacts has been examined for doses in the range 1013-1015 ions/cm2. Measurements of specific contact resistance, ρc, were performed using the two-contact circular test structure. The magnitude of ρc for the Ti/Ni/Au contacts on unimplanted SiC was 1.29 x 10−6 Ω.cm2. The value of ρc increased significantly at an implant dose of 1 x 1015 ions/cm2. The dependence of ρc on ion dose has been measured using both C and P implant species.

In this study, the growth of LbL film of polyallylamine hydrochloride (PAH), polyvinyl sulfonic acid (PVS) and glucose oxidase (GOx) in porous anodic alumina substrate (PAA) was accompanied by total reflectance technique. The PAA substrate was synthesized with aluminum anodisation and sample morphology was characterized by scanning electron microscopy (SEM).

The emergence of 2-dimensional (2D) materials could herald numerous advanced scientific methodologies for both fundamental and applied research. These ultrathin materials can be functionalized and, thus, have the potential to make new devices and sensors that are both highly efficient and sensitive. In addition to being mechanically robust, the 2D materials can be engineered to provide sensor architectures that further increase their inherent high surface area by creating 3D geometries using layer by layer assembly to make stacked devices that could potentially be transparent. The increased sensor surface area would deliver increased signal-to-noise and sensitivity. Here highly sensitive and selective electrochemical detection of bio-analytes using some of engineered 2D materials such as graphene nano-ribbons, fluorinated graphene, and molybdenum disulfide is presented. It is found that surface moieties, defects and surface charges in these ultra-thin layers result in enhanced electron transfer kinetics between the electrodes and biomolecules. This in turn results in an oxidation or reduction of biomolecules with a high peak current, indicating the possible uses of 2D materials for various point-of-care devices. A novel stable 3D electrode geometry has been found to have enhanced heterogeneous electron transfer properties compared to 2D electrodes and provides evidence that electrode geometry and surface area could significantly impact the performance of biosensors.

Polymer-based therapeutic strategies require biomaterials with properties and functions tailored to the demands of specific applications leading to an increasing number of newly designed polymers. For the evaluation of those new materials, comprehensive biocompatibility studies including cyto-, tissue-, and immunocompatibility are essential. Recently, it could be demonstrated that star-shaped amino oligo(ethylene glycol)s (sOEG) with a number average molecular weight of 5 kDa and functionalized with the phenol-derived moieties desaminotyrosine (DAT) or desaminotyrosyl tyrosine (DATT) behave in aqueous solution like surfactants without inducing a substantial cytotoxicity, which may qualify them as solubilizer for hydrophobic drugs in aqueous solution. However, for biomedical applications the polymer solutions need to be free of immunogenic contaminations, which could result from inadequate laboratory environment or contaminated starting material. Furthermore, the materials should not induce uncontrolled or undesired immunological effects arising from material intrinsic properties. Therefore, a comprehensive immunological evaluation as perquisite for application of each biomaterial batch is required. This study investigated the immunological properties of sOEG-DAT(T) solutions, which were prepared using sOEG with number average molecular weights of 5 kDa, 10 kDa, and 20 kDa allowing analyzing the influence of the sOEG chain lengths on innate immune mechanisms. A macrophage-based assay was used to first demonstrate that all DAT(T)-sOEG solutions are free of endotoxins and other microbial contaminations such as fungal products. In the next step, the capacity of the different DAT(T)-functionalized sOEG solutions to induce cytokine secretion and generation of reactive oxygen species (ROS) was investigated using whole human blood. It was observed that low levels of the pro-inflammatory cytokines interleukin(IL)-1β and IL-6 were detected for all sOEG solutions but only when used at concentrations above 250 µg·mL-1. Furthermore, only the 20 kDa sOEG-DAT induced low amounts of ROS-producing monocytes. Conclusively, the data indicate that the materials were not contaminated with microbial products and do not induce substantial immunological adverse effects in vitro, which is a prerequisite for future biological applications.

In this study, we investigated the influence of line defects consisting of pentagon-heptagon (5-7) pairs on the electronic transport properties of zigzag-edged and armchair-edged graphene nanoribbons (GNRs). Using the first-principles density functional theory, we study their electronic properties. To investigate their current-voltage (I-V) characteristics at low bias voltage (∼ 1 meV), we use the nonequilibrium Green’s function method. As a result, we found that the conductance of the GNRs having a connected line defect between source and drain shows better performance than that of the ideal zigzag-edged GNRs (ZGNRs). A detailed investigation of the transmission spectra and the wave function around the Fermi level reveals that the line defects arranged along the transport direction work similar to an edge state of the ZGNRs and can be an additional conduction channel. Our results suggest that such a line defect can be effective for low-resistance GNR interconnects.

In this work we examine the electrical characteristics and the memory properties of metal-alumina-nitride-oxide-silicon (MANOS) devices as a function of the post deposition annealing conditions. Post deposition annealing of the samples was performed at 850 or 1050 °C in nitrogen ambient using two different processes: (1) Furnace annealing for 15 min and (2) rapid thermal annealing for 1 or 5 min. The capacitance equivalent thickness as extracted from the capacitance voltage characteristics depends strongly on the annealing process, being smallest for the furnace annealing. Furthermore, the experimental results indicate that the type of the annealing determines the defect state density of the Al2O3 layer, via which the undesired effect of gate electrode electron injection takes place in the negative voltage regime. For inert ambient annealing the furnace process appears more efficient as compared to RTA.

Three methacrylic polymers bearing (phenylene)azobenzene moieties in the side-chain were synthesized via free-radical polymerization of monomer (E)-6-(4-((3’-cyano-4’-(hexyloxy) -[1,1’- biphenyl]-4-yl) diazenyl) phenoxy) hexyl methacrylate using 1, 5 and 10 mol% of 1,1’-azobis(cyclohexanecarbonitrile) (ABCN) as initiator. The chemical structures of monomer and polymers were confirmed by 1H NMR and FT-IR spectroscopies. Analysis by gel permeation chromatography (GPC) showed average molecular weights (Mw) of 1.0x105, 7.3x104, and 4.5x104 g/mol for polymers P1%, P5%, and P10%, respectively. These results indicate a clear dependence of the Mw on the amount of initiator used; the higher the amount of ABCN, the lowest the molecular mass. Thermotropic liquid-crystalline properties were analyzed by differential scanning calorimetry (DSC) and polarized optical microscopy (POM). All polymers showed a liquid-crystalline behavior over a wide range of temperatures (>100°C) displaying smectic type mesophases. A small shift (around 8°C) upwards in the clearing temperature was observed on increasing the molecular masses from P10% to P1%. The trans-cis photo-isomerization of polymers was studied in solution and in thin films by UV-Vis spectroscopy. High cis-isomer contents in solution (>90%) were reached in relative short irradiation times.

Mass spectrometry is one of the primary analysis techniques for biological analysis but there are technological barriers in sampling scale that must be overcome for it to be used to its full potential on the size scale of single cells. Current mass spectrometry imaging methods are limited in spatial resolution when analyzing large biomolecules. The goal of this project is to use atomic force microscope (AFM) tip enhanced laser ablation to remove material from cells and tissue and capture it for subsequent mass spectrometry analysis. The laser ablation sample transfer system uses an AFM stage to hold the metal-coated tip at a distance of approximately 10 nm from a sample surface. The metal tip acts as an antenna for the electromagnetic radiation and enables the ablation of the sample with a spot size much smaller than a laser focused with a conventional lens system. A pulsed nanosecond UV or visible wavelength laser is focused onto the gold-coated silicon tip at an angle nearly parallel with the surface, which results in the removal of material from a spot between 500 nm and 1 µm in diameter and 200 and 500 nm deep. This corresponds to a few picograms of ablated material, which can be captured on a metal surface for MALDI analysis. We have used this approach to transfer small peptides and proteins from a thin film for analysis by mass spectrometry as a first step toward high spatial resolution imaging.

Fe-Co-B was identified as a potential candidate for the development of high-frequency sensors and high-frequency actuators. To fabricate high-frequency magnetostrictive resonators, Fe-Co-B magetostrictive thin films were prepared by combining electrochemical deposition and microfabrication processes. It is crucial to obtain thin films with proper microstructure and composition. Results showed that Fe-rich Fe-Co-B thin films exhibited better resonance behavior than those with Co-rich and equiatomic Fe and Co compositions. It is also found that the deposition condition plays an important role on the performance of the films. Fe55Co28B17 thin films were fabricated under the same current density for different times. The films exhibited nanocrystalline structure, circular nodules as surface morphology and good resonance behavior. Fe/Co ratio on surface and cross section slightly decreased with increasing the deposition time. The resonance frequency slightly increased and the Q value was found to decrease with increasing deposition time.

Lithographically fabricated gold nanowires are optically excited with 532nm CW laser and the local temperature change is measured in air, pure water and various concentration aqueous solutions of ionic solutes NaCl, Na2SO4 and MgSO4 using the thermal sensor film of Al0.94Ga0.06N embedded with Er3+ ions. The interface thermal resistance for heat transfer from the excited nanowires into the surrounding liquid is determined from the slopes of the temperature change versus laser intensity plots obtained for the nanowire excitation under various solutions. Addition of ionic solute molecules into the solution decreases the interface thermal resistance and hence leads to increased heat dissipation into the surrounding liquid. Interface thermal resistance decreases exponentially with the ionic strength of solution and saturates around zero for solution ionic strength of 0.3M and higher.

One of the main areas of improvement in capacitive deionization technologies is the materials used for electrodes which have very specific requirements. In the present work, a wide range of material characterization techniques are employed to determine the suitability of a multiwall carbon nanostructure thin film as electrode material. The electrical, mechanical, surface and wetting characteristics are studied proving the membrane highly conductive (σ=7.25 103 S/m), having competitive electro-sorption capacity (11.7 F/g at 10 mV/s) and surface area (149 m2/g), strain rate dependent mechanical properties and hydrophobic wetting behavior.

We herein report the optical and cytotoxicity properties of highly luminescent water soluble mercaptopropanoic acid (MPA) capped CdTe/CdSe core shell nanoparticles (NPs). The synthesis of the CdTe/CdSe NPs was carried out via a simple, one pot and economical route, involving the use of greener materials under ambient environment in the absence of an inert atmosphere. The temporal evolution of the size and optical properties of the nanomaterials was investigated by varying the reaction time and stability of the as-synthesised material at pH 12. The as-synthesised nanomaterials were characterised using UV-vis absorption and photoluminescence (PL) spectroscopy. The nanoparticles obtained were of high quality with high absorption and emission features. Addition of Se precursor to produce CdSe layer on the CdTe NPs core surface resulted in significant red shirt of both the absorption and emission maxima. The stability study showed that the emission maximum peak positions and FWHM remain the same with increase in emission intensity for all the NPs during the aging period. The cytotoxicity assay showed very high cell viability for the CdTe/CdSe NPs produced at 7 h compared with those produced at 30 mins as the concentration increased from 0.1 to 60 ug/ml. The lower cytotoxicity at the higher reaction time was attributed to the higher stability of the material and hence lower release of Cd2+.

Here we report our study of the electronic properties of [100]-textured gadolinium nitride (GdN) thin films synthesized using a chemical vapor deposition (CVD) method. The electronic properties of the films were investigated using photoemission and inverse photoemission spectroscopy coupled with computational modeling. Our density functional theory (DFT) calculations suggest that the theoretically predicted half-metallic electronic structure of GdN is likely due to its low density of states (DOS) at the Fermi level. These calculations are supported by our photoemission and inverse photoemission spectroscopic measurements which show a band gap for the prepared films of a few milli-electron volts, seemingly consistent with the predicted electronic structure. Additionally, the use of a CVD gallium nitride capping layer was found to decelerate the surface oxidation of our GdN samples.