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We present an integrated readout technique for interrogating the suspension height of micro-electro-mechanical systems (MEMS) structures. This readout technique is envisaged to be useful in applications such as MEMS-based biological and chemical sensing, where it is necessary to obtain the accurate position of a MEMS beam. The approach is based on the suspended MEMS structure modulating light transmission in an underlying optical waveguide via Fabry-Perrot phenomena. The performance of the technique is predicted via finite difference time domain (FDTD) simulations the results of which are confirmed by experimental measurements.
Cartilage is a complex biological tissue that exhibits gel-like behavior. Its primary biological function is providing compressive resistance to external loading and nearly frictionless lubrication of joints. In this study, we model cartilage extracellular matrix using a biomimetic system. We demonstrate that poly(vinyl) alcohol (PVA) hydrogels are robust biomaterials exhibiting mechanical and swelling properties similar to that of cartilage extracellular matrix. A comparison is made between the macroscopic behavior of PVA gels and literature data reported for cartilage.
The aim of the present study is to analyze interfacial adhesion and characterize the tensile properties of a FML elaborated from thin layers of an aluminum alloy and layers of maleic anhydride modified polypropylene (MAHPP) reinforced with an aramid woven fabric. For the analysis of interfacial adhesion, a microbond test is carried out on the MAHPP-aramid fiber system and a single lap joint test is performed on FML constituent materials, as well as the tensile characterization of the FML and its constituents is conducted accordingly. Microbond testing revealed an improvement in interfacial shear strength for the MAHPP-aramid fiber system in comparison with that of polypropylene-aramid fiber systems reported in the literature. The apparent shear strength between the FML constituent materials is comparable to that for bonding of aluminum with MAHPP. Tensile characterization of the FML and its constituents showed that the FML presented greater tensile strength than the aluminum alloy; and a more ductile behavior in comparison with its individual components due to the degree of adhesion between the constituents which allows the material to deform in unison.
Combining high resolution transmission electron spectroscopy, electron diffraction, and resonant Raman spectroscopy experiments on the same suspended (free-standing) individual carbon nanotubes is the ultimate approach to relate unambiguously the structure and the intrinsic phonon features of these nano-systems.
By using this approach, the effect of coupling between nanotubes on the phonons is investigated in two model nano-systems: (i) a bundle of two non-identical SWNTs (inhomogeneous dimer), (ii) double-walled carbon nanotubes.
Hydrogel actuators were prepared by combining ionoprinting technique with reversible metal ion coordination chemistry found in mussel adhesive proteins. Hydrogels were formulated with biomimetic dopamine moiety, which contains a catechol side chain that is capable of forming mono-, bis-, and tris-complexes with ferric (Fe3+) ions with increasing pH. Catechol-Fe3+ complexation increased local crosslinking density, which induced hydrogel bending at the site of Fe3+ ionoprinting. The effect of pH on the dynamic response of hydrogel actuation was tracked by following the radius of curvature at the ionoprinting site. Both the rate of change and the maximum radius of curvature increased when the pH with increasing pH (2.5-9.5), indicating that pH can be used to modulate hydrogel actuation. Additionally, hydrogels containing Fe3+ demonstrated higher extent of deswelling when equilibrated at a basic pH. Similarly, dynamic mechanical analysis in the compression mode revealed that both the storage and loss modulus values for Fe3+-containing hydrogels increased with increasing pH. These results indicated that bis- and tris-complexes formed at an elevated pH level contributed to a faster rate of actuation and a more condensed network architecture. Hydrogel actuation and deswelling were also observed at pH of 3.5 although to a lesser degree, potentially due to a stronger affinity between network-bound catechol and Fe3+ ions as compared to complexes formed in a dilute solution.
Drug delivery systems are becoming increasingly sophisticated, with the ability to target and penetrate specific tissues and release drugs based upon the local environment. While these advanced systems often offer advantages over their less sophisticated counterparts, the final product may be more complex and require additional manufacturing steps. In this article, we review a body of work based on genetically encoded elastin-like polypeptides (ELPs) that offer a route to modular, multifunctional delivery systems that are simple to manufacture. ELPs are temperature-sensitive biopolymers that can be designed on the genetic level and expressed in cell-based protein production systems. The tools of molecular biology and versatility of proteins are used to engineer polymers with precise composition and molecular weight that self-assemble to form drug delivery systems with an impressive variety of features and functions. Due to their versatility and ease of production, ELPs are likely to contribute to the goal of designing simple and effective “smart” delivery systems.
Alumina-silicone hybrid nanolaminate films were synthesized by plasma enhanced chemical vapor deposition (PECVD) process. PECVD allows digital control over nanolaminate construction, and may be performed at low temperature for compatibility with flexible substrates. These materials are being considered as dielectrics for application such as capacitors in thin film transistors and memory devices. Temperature dependent electrical and dielectric properties of the nanolaminate dielectric films in metal-insulator-metal structures are taken in the range of 200- 340 K to better asses their potential applications for different devices. It is observed that the frequency dependent dielectric constant (εr) and ac conductivity (σac) increase with the temperature. Both quadratic (α) and linear (β) voltage coefficient of capacitance (VCC) increases as the temperature increases. The temperature co-efficient of capacitance (TCC) decreases from 894 to 374 ppm/K as the Al2O3 composition increases in the alumina/silicone nanolaminates. Activation energy (Ea) for hopping conduction mechanism varies from 0.011 eV to 0.008 eV as the alumina composition increases from 50 to 83.3%.
Spent nuclear fuel from TVO's (Teollisuuden Voima Oy) and Fortum's nuclear power plants will be deposited deep in the crystalline bedrock in Olkiluoto, Western Finland. The bedrock needs to be well characterized to assess the risks inherent to the waste disposal at the site. If radionuclides (RN) are transported, it happens via water conducting fractures. Retardation may occur either by diffusion into stagnant pore water or by immobilization on mineral surfaces of the rock matrix.
RN’s retardation from flowing water is linked to parameters defining porosity and microscopic rock pore structure, such as pore size distribution, connectivity, tortuosity and constrictivity, and by the mineralogy and chemical nature of the minerals and charge of the pore surfaces.
In this work, centimeter scale rock cores from Olkiluoto were investigated. The work is part of the in situ project REPRO (Experiments to investigate Rock Matrix Retention Properties) where the diffusion and sorption of RN are studied experimentally. Porosity and pore structures were characterized with the PMMA autoradiography method and polarized microscopy, which was used also to ascertain the mineralogy of the samples.
The results show that the rock from the REPRO site has low porosity with a mean value of 0.5% and a range of 0.1-1.5%. Rock heterogeneity explains the variation of porosity values. Correlation between the porosity and the mineralogy was found. Areas of high porosity correspond to areas of altered minerals, such as cordierite, biotite and plagioclase, which cover spatially between 10 and 20% of the rock volume
Modern polypropylene film power capacitors are state of the art for power factor correction and many DC link applications, but their long-term commercial use is limited to temperatures of less than 85°C. The temperature limit is given by the dielectric polypropylene which has a melting point in the range of 140 to 170°C, while glass is much higher. Thus, the temperature limit could potentially be overcome by use of thin, alkali-free glass as dielectric. “Glass capacitors” employing ultra-thin and high purity glass layers are promising devices for high temperature applications in oil, gas, aerospace, hybrid electric vehicles, DC transmission, and pulsed power systems. This includes emerging power electronic systems using silicon carbide switches and diodes.
This work analyzes and compares various glasses with a thickness of less than 50 µm by dielectric spectroscopy and elemental analysis. It is demonstrated that glass is attractive as dielectric for a wide frequency range up to 200°C. It argues that the dielectric losses are currently too great for thin glass to be used within a commercial power capacitor.
While high temperature prototypes already exist, we demonstrate through our analysis that further developments are required to integrate this promising device into commercial systems. It is seen that even trace amounts of alkali materials can have an impact on losses. These losses must be further reduced through fundamental research into polarization/conduction mechanisms of various glass components.
Peptides have become attractive molecules for fabricating biomaterials. Studies of peptide structure, assembly properties, and dynamic behavior in response to external parameters have led to rational novel design of peptide biomaterials. One model sequence selected was a β-spiral motif of spider flagelliform silk protein, [GPGGX]n (X = any amino acid). Modifying the X residue can change the quantity of secondary structure and the stability of this spider silk motif. Glycine provides flexible properties, and proline influences the secondary structure and mechanical properties. Another model sequence was GXGXDXUX (U = hydrophobic residue), a Ca2+ binding domain of lipase Lip A from Serratia marcescens, in which aspartate residue is required for ion binding. Combining with [GPGGX]n, we rationally designed peptide as GPGGDGPGGD (eD2). The Ca2+ binding sequence was hidden in the first eight residues of eD2. As expected, this peptide can assemble into nanofibrils triggered by Ca2+ ions. Using the segment FLIVIGSII (h9) from the third trans-membrane segment of subunit IV in the dihydropyridine sensitive human muscle L-type calcium channel as the hydrophobic motif, we obtained FLIVIGSIIGPGGDGPGGD (h9e) peptide. The h9e self-assembled into nanofibrils and further formed shear-thinning and rapid recovery hydrogel in neutral pH range from 6.0 to 8.0 with a large working range of temperature. NMR study showed that amphiphilic structure of h9e peptide tended to adopt a more helical structure during hydrogel formation. The h9e peptide has great potential for biomedical applications. MCF-7 cells were successfully grown as colony-like clusters (reminiscent of real tumors) in h9e hydrogel system. The drug response test of cisplatin further demonstrated the capability of h9e system for drug screen. Moreover, h9e hydrogel showed a promising adjuvanticity by enhancing the vaccine efficacy for killed H1N1 swine influenza virus and PRRS modified live virus.
The sensor team at the Los Alamos National Laboratory is an integrated multidisciplinary group that develops both core technologies as well as accessory tools for efficient biodetection. We have developed a waveguide-based optical biosensor for the efficient and ultra-sensitive, rapid detection of biological agents. We have previously demonstrated the use of this technology for the detection of biomarkers associated with many diseases. Herein, we present the preliminary data demonstrating the extension of this technology to the discovery and detection of Traumatic Brain Injury (TBI). TBI afflicts a significant percentage of US troops deployed in Iraq and Afghanistan, but is difficult to diagnose efficiently. Currently, only neuropsychological questionnaires are being used for the diagnosis of this condition, which can range from mild concussion to severe brain damage. The ultimate goal of this project is to develop a rapid biomarker-based diagnostic for TBI in blood. However, this cannot be accomplished until a comprehensive repertoire of biomarkers secreted during brain injury is established. This requires an integrated biomarker discovery and detection approach that is sampled directly from human serum and cerebrospinal fluid.
The results reported here are preliminary steps in that direction wherein we aim to develop two different methods for the discovery of novel biomarkers of TBI in blood and cerebrospinal fluid, as well as develop assays for two biomarkers on an ultra-sensitive waveguide-based platform that was developed at LANL. We were able to evaluate two different methods for biomarker discovery: Matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) and two dimensional gel electrophoresis (2-DE) in serum samples. In addition to development of depletion protocols to remove abundant proteins in serum, we were also able to detect spiked TBI biomarkers using both methods. However, the results clearly show that for protein biomarkers, MALDI MS is much more sensitive than 2-DE. We also developed a sandwich immunoassay on a waveguide-based platform for a TBI biomarker, procalcitonin, using commercially available antibodies. We show with our methods that we were able to directly detect procalcitonin from human serum. While our discovery and detection methods show promising results, these methods need to be further optimized before we can apply it to clinically relevant samples.
We have investigated the photon-energy dependence of nonlinear optical absorption in graphene in the near infrared (NIR) and visible range (1.13 – 3.1 eV). Two nonlinear processes, namely one-photon interband absorption saturation and two-photon absorption (2PA), have been unambiguously determined in high-quality, CVD-grown, multilayer graphene films with using femtosecond Z-scan technique. The absorption saturation is found to have a square dependence on the photon energy. The 2PA spectrum is measured to be close to the theoretical prediction of ω-4 dependence at NIR wavelengths. In the visible range, however, the photon-energy dependence of 2PA is dominated by the excitonic Fano resonance.
Silver thin films are used as a functional layer in many applications such as low-emissivity and solar control coatings on glass for insulating windows, as well as transparent conducting electrodes for OLEDs and PV. For these applications, the conductivity of the film is critical; it is linked to the crystallinity and the grain size of silver layers which thickness ranges from 5 to 15nm. Such coatings often undergo thermal treatments up to 700°C aimed at toughening the glass substrate or improving the coating itself by promoting grain growth and curing point defects. This treatment can however dramatically damage the silver layer by inducing the formation of defects in the layer, such as holes or silver domes, decreasing both conductivity and light transmission of the coatings. Because of the extreme thinness of the films (less than 15 nm), the investigation of these phenomena requires in situ imaging at the nanoscale. In this study, grain growth and defects formation were observed in 15 nm-thick Ag films encapsulated with zinc oxide and silicon nitride using Transmission Electron Microscopy with in-situ heating from ambient temperature to 600°C. Significant grain growth was found to occur only from 400°C, and from 500°C holes in the silver layer started to form and grow, as well as thick silver domes formed by dewetting. Irradiation by the electron beam was also found to cause grain growth.
Electrical and Optical measurements were carried out on permalloy oxide (PyO) thin films made by reactive dual ion beam sputtering at room temperature. VSM measurements at room temperature and 15 Kelvin did not reveal any magnetic moment in 120 nm thick films. The optical refraction and extinction spectra from 200-1000 nm were determined from ellipsometry measurements using a Cody-Lorentz model and provided in a reproducible method to determine the film thickness of PyO films on different substrate materials. PyO is transparent above 700 nm and is strongly absorbing below 500 nm. The resistivity values of PyO samples sputtered at room temperature depend on the oxygen flow rate and is approximately 4E3 Ohm cm for films prepared at 10 sccm. The resistivity of PyO decreases as a function of temperature. The dielectric constant is strongly frequency dependent, decreasing from 500 at 500 Hz to 10 at 1 MHz.
Recent experimental evidence on nano-particle and nano-wire silicon anodes showed an initial rapid velocity of reaction front at the initial stage of lithiation, followed by an apparent slowing or even halting of the reaction front propagation. This intriguing phenomenon is attributed to the lithiation-induced mechanical stresses across the reaction front which is believed to play an important role in the kinetics of reaction at the front. Here, through theoretical formulation, we presented a comprehensive study on lithiation-induced stress field and its contribution to the driving force of lithiation in hollow spherical anodes with different boundary conditions at the inner surface of the particle. Our results reveal that hollow spherical silicon anodes can be lithiated more easily than solid spherical silicon particles and thus may serve as an optimal design of high performance anodes of lithium-ion battery.
We present preliminary results on a processing protocol by chemical activation that transforms organic waste product such as coconut husk into high surface area activated carbon. Dried raw materials of the coconut husk were carbonized anaerobically into char. The char was impregnated with KOH of different ratios and were activated at 800°C and 900°C. The transmission electron microscope was used to acquire structural and morphological information of the activated carbon, and the surface area and porosity analysis were performed using Micromeritics ASAP 2020 analyzer. The activated carbons show both micropores and mesopores with specific surface area as high as 2900m2/g.
The migration behavior of plutonium is expected to be affected by the corrosion products of carbon steel in compacted bentonite at high-level waste repositories. Electrochemical experiments were carried out to simulate the reducing environment created by ferrous iron ions in equilibrium with anoxic corrosion products of iron. The concentration profiles of plutonium could be described by the convection -dispersion equation to obtain two migration parameters: apparent migration velocity Va and apparent dispersion coefficient Da. The apparent migration velocity was evaluated within 1 nm/s and was found to be independent of the experiment duration and the dry density of bentonite in the interval 0.8-1.4 Mg/m3. The apparent dispersion coefficient increased with the experiment duration at a dry density of 1.4 Mg/m3. The results for other dry densities also showed the same trend. These findings indicate that plutonium migration likely starts after ferrous ions reach the plutonium, in other words, the reducing environment due to ferrous ions could change the chemical form of plutonium and/or the characteristics of compacted bentonite. The apparent diffusion coefficient was estimated to be around 0.5 to 2.2 µm2/s and increased with decreasing the dry density of bentonite.