Minipressure sensor using AlGaN/GaN high electron mobility transistors

AlGaN/GaN high electron mobility transistors (HEMTs) with polar and nonpolar ZnO nanowires modified gate exhibit significant changes in channel conductance upon expose to different concentration of carbon monoxide (CO) at room temperature. The ZnO nanowires, grown by chemical vapor deposition (CVD), with perfect crystal quality will attach CO molecule and release electrons, which will lead to a change of su rface charge in the gate region of the HEMTs, inducing a higher positive charge on the AlGaN surface, and increasin g the piezoinduced charge density in the HEMTs channel. These electrons create an image positive char ge on the gate region for the required neutrality, thus increasing the drain current of the HEMT s. The HEMTs source-drain current was highly dependent on the CO concentration. The limit of detection achieved was 400 ppm and 3200ppm in the open cavity with continuous gas flow using a 50 ™ 50 P m 2 gate sensing area for polar and nonpolar ZnO nanowire gated HEMTs sensor.

To obtain a better understanding of the short term reactions between sulfate and hydrous alumina the relationships between the amount of sulfate retained by the alumina and reaction time, concentration, ligands displaced by sulfate, and changes in surface charge were studied. Experimental conditions were 3 hours reaction time, 0.01 M NaCl medium, pH 5.0, 30°C, and nitrogen atmosphere. Sulfate adsorption was very rapid and about 90% of the reaction was over in 10 min. There was little change in adsorption after 3 hours. The adsorption increased with increasing final solution concentration up to about 6 µeq/ml after which it decreased. Sulfate adsorption resulted in the release of OH ‐ from, and the neutralization of positive charge on the surface. From the quantitative relationships between sulfate adsorbed, the ligands displaced, and the changes in surface charge it is proposed that sulfate is adsorbed on hydrous alumina as SO 4 2‐ bridging across two aluminum atoms, forming a six‐membered ring. At low concentrations sulfate preferentially displaces aquo groups (Al‐OH 2 ) from the positive sites. With increasing concentration, increasing proportions of hydroxo groups (Al‐OH) from the neutral sites are displaced. The decrease in adsorption above 6 µeq/ml of sulfate concentration is inexplicable at this stage.

The characteristics of Pt/GaN Schottky diodes and Sc/sub 2/O/sub 3//AlGaN/GaN metal-oxide semiconductor (MOS) diodes as hydrogen and ethylene gas sensors and of gateless AlGaN/GaN high-electron mobility transistors (HEMTs) as polar liquid sensors are reported. At 25/spl deg/C, a change in forward current of /spl sim/6 mA at a bias of 2 V was obtained in the MOS diodes in response to a change in ambient from pure N/sub 2/ to 10% H/sub 2// 90% N/sub 2/. This is approximately double the change in forward current obtained in Pt/GaN Schottky diodes measured under the same conditions. The mechanism appears to be formation of a dipole layer at the oxide/GaN interface that screens some of the piezo-induced channel charge. The MOS-diode response time is limited by the mass transport of gas into the test chamber and not by the diffusion of atomic hydrogen through the metal/oxide stack, even at 25/spl deg/C. Gateless AlGaN/GaN HEMT structures exhibit large changes in source-drain current upon exposing the gate region to various polar liquids, including block co-polymer solutions. The polar nature of some of these polymer chains lead to a change of surface charges in gate region on the HEMT, producing a change in surface potential at the semiconductor/liquid interface. The nitride sensors appear to be promising for a wide range of chemicals, combustion gases and liquids.

Large pressures can induce detrimental deformation in micro- and nanofluidic channels. Although this has been extensively studied for systems driven by pressure and/or capillary forces, deflection in electrokinetic systems due to internal pressure gradients caused by non-uniform electric fields has not been widely explored. For example, applying an axial electric field in a channel with a step change in conductivity and/or surface charge can lead to internally generated pressures large enough to cause cavitation, debonding, and/or channel collapse. Finite electric double layers within nanofluidic channels can further complicate the physics involved in the deformation process. In order to design devices and experimental procedures that avoid issues resulting from such deformation, it is imperative to be able to predict deformation for given system parameters. In this work, we numerically investigate pressures resulting from a step change in conductivity and/or surface charge in micro- and nanofluidic channels with both thin and thick double layers. We show an explicit relation of pressure dependence on concentration ratio and electric double layer thickness. Furthermore, we develop a numerical model to predict deformation in such systems and use the model to unearth trends in deformation for various electric double layer thicknesses and both glass and PDMS on glass channels. Our work is particularly impactful for the development and design of micro- and nanofluidic-based devices with gradients in surface charge and/or conductivity, fundamental study of electrokinetic-based cavitation, and other systems that exploit non-uniform electric fields.

The immobilization of thiol-derivatized DNA on a Au (111) single crystal surface by self-assembly has been investigated by electrochemical scanning tunneling microscopy (EC-STM). Continuous potential-dependent orientation changes of double-stranded oligodeoxynucleotides (ODN) have been observed in a certain potential range from 200 to 600 mV (versus SCE). It is suggested that the DNA duplexes stand straight on the gold surface at potentials negative of the potential of zero charge (pzc) and then lay down on the surface when the potential shifts positively. These results are in agreement with the expectation based on the Coulombic interaction consideration between negatively charged DNA helices and gold surface. As the applied potential shifts positively, the surface charge changes from negative to positive, that is, the Coulombic force between negatively charged DNA helices and gold surfaces changes from repulsion to attraction. However, for the single-stranded oligodeoxynucleotides, no distinct changes in the surface structure were observed with the applied potential.

Lung cancer is the leading cause of cancer deaths in the world, among both men and women. It claims more lives each year than do colon, prostate, ovarian and breast cancers combined. Currently, diagnosis of lung cancer in stages I and II is very difficult and hence prognosis is delayed, leading to increased mortality rate. Carcinoembryonic antigen (CEA), is a common cancer biomarker and the expression of CEA above 5 ng/mL is suggestive of the presence of cancer. In this study, we utilize immunology, which is antibody/antigen reaction, with the combination of High Electron Mobility Transistor (HEMT) as the transducer, to develop a biosensor for detecting lung cancer biomarkers, electronically, as opposed to traditional ELISA techniques. HEMTs have already been demonstrated in gas, ion and biomolecule sensing purpose. When analytes accumulate on the gate area, the net charge on the HEMT surface changes. This electrical detection technique is simple, fast, and convenient. The detecting signal from the gate is amplified through the drain-source current, making the sensor very sensitive. Figure 1 (a) and (b) show the schematic of AlGaN/GaN HEMT and the top-view of the device. To create a high quality HEMT device, a 3 μm-thick undoped GaN buffer layer and a 150 Å-thick undoped Al0.25Ga0.75N layer were deposited by metal-organic chemical vapor deposition (MOCVD) on the substrate. Mesa isolation was formed by Inductively Coupled Plasma (ICP) etching system for 28 seconds. Ti, Al, Ni and Au were deposited by Electron Beam Evaporation and were annealed at 850 °C for 45 seconds under N2 flowing to form ohmic contacts. Passivation was provided by encapsulating the device with photoresist, with only the gate region open for antibody immobilization using photolithography. After sensor fabrication, surface functionalization is carried out by thiol binding on gold. We mixed bi-functional thio-carboxylate with the CEA antibody and let the antibody bind with the carboxyl functional group by EDC-sulfo NHS coupling reaction. Then the device is incubated in this solution for 12 hours at 4 ºC. BSA is used for surface blocking and as a protein dilution buffer. For the sensor measurement, source-drain bias is fixed at 0.5 V and the current change induced by binding of CEA was measured by applying a 0.5 V gate voltage. Figure 1 (c) shows the total charge accumulated for various concentrations of CEA. This can be used as an index to quantify the amount of CEA present in sample as it can distinguish various protein concentrations even in the physiological blood/serum concentration (1x PBS). The change in total charge with varying concentration of CEA can thus represent sensor calibration curve. Comparing to the conventional methods, the electronic detection of CEA using HEMT has the advantages of high sensitivity and low response time. We believe this method has the potential to further the research in the field of electronic biosensors. Figure 1

[This retracts the article DOI: 10.1021/acsomega.0c02518.].

: Stimulus-induced changes in surface properties of nanoassemblies have been of interest in a variety of applications. One such change involves change in surface charge. Changes in surface charge can be conveniently assayed using interaction of the nanoassemblies with cells. We have utilized the nanoassembly-cell interaction to investigate the pH-induced changes in surface properties. Similarly, surface functionalization of nanoparticles and host-guest properties of nanoassemblies are two critical features in the utilization of nanostructures in a variety of applications in materials, chemical, and biological nanotechnology. However, simultaneously incorporating these two features in one nanoparticle design is a rather challenging task. We were interested in developing a simple approach for functionalizable polymer nanoparticles, where we stipulated that: (i) the precursor polymer is based on a random copolymer, which is synthetically accessible; (ii) the polymer self-assembles in a solvent, which can then be converted to nanoparticle in one step without the need for any additional processing; (iii) the nanoparticle contains a surface functional group, which can be further manipulated easily; (iv) the size of the nanoparticle is tunable; and (iv) the interior of the nanoparticle is capable of sequestering guest molecules.

Change in surface charge density and membrane potential of intact mitochondria during energization

The luminal plasmalemma of regenerating mesothelial cells was examined by transmission electron microscopy and the concentration of microvilli at various stages of healing was quantified. Charged tracer and lectin binding techniques were also employed to investigate electrostatic and chemical changes in mesothelial glycocalyx. In uninjured mesothelium and at all stages of healing, the concentration of microvilli at the cellular periphery was greater than over the main cell mass (P < 0.05). Furthermore, there was an increase in the concentration of microvilli in all regions by day 4, which reached a maximum at day 6, then at days 10-15 returned to values closer to uninjured mesothelium (P < 0.01). These changes were associated with an alteration in surface charge. In all lesions, the surface charge on microvillar membranes was greater than for flat membranes, but the difference was only significant at days 4, 6, and 15 (P < 0.001). The changes in surface charge may reflect a differential expression of mucopolysaccharides on the surface membrane. In addition, concanavalin A bound avidly to mesothelial surface membranes, suggesting the presence of alpha-methyl-D-mannoside residues. These findings suggest an association between microvillar formation and surface charge, the former protecting the healing mesothelium by enhancing entrapment of serosal fluid and its contents.

Modelling of PFAS-surface interactions: Effect of surface charge and solution ions

ABSTRACTAu-gated AlGaN/GaN High Electron Mobility Transistor (HEMT) structures were functionalized in the gate region with label free 3′-thiol modified oligonucleotides. This serves as a binding layer to the AlGaN surface for hybridization of matched target Deoxyribonucleic Acid (DNA). X-ray photoelectron spectroscopy (XPS) shows that immobilization of thiol modified DNA covalently bonded with gold on the gated region. Hybridization between probe DNA and matched or mismatched target DNA on the Au-gated HEMT was detected by electrical measurements. The HEMT drain-source current showed a clear decrease of 115 μA as this matched target DNA was introduced to the probe DNA on the surface, showing the promise of the DNA sequence detection approach for biological sensing.

The drain current fluctuation of ungated AlGaN/GaN high electron mobility transistors (HEMTs) measured in different fluids at a drain-source voltage of 0.5 V was investigated. The HEMTs with metal on the gate region showed good current stability in deionized water, while a large fluctuation in drain current was observed for HEMTs without gate metal. The fluctuation in drain current for the HEMTs without gate metal was observed and calculated as standard deviation from a real-time measurement in air, deionized water, ethanol, dimethyl sulfoxide, ethylene glycol, 1,2-butanediol, and glycerol. At room temperature, the fluctuation in drain current for the HEMTs without gate metal was found to be relevant to the dipole moment and the viscosity of the liquids. A liquid with a larger viscosity showed a smaller fluctuation in drain current. The viscosity-dependent fluctuation of the drain current was ascribed to the Brownian motions of the liquid molecules, which induced a variation in the surface dipole of the gate region. This study uncovers the causes of the fluctuation in drain current of HEMTs in fluids. The results show that the AlGaN/GaN HEMTs may be used as sensors to measure the viscosity of liquids within a certain range of viscosity.

AlGaN/GaN HEMT based hydrogen sensor with platinum nanonetwork gate electrode

Concentration polarization-enhanced radical graft polymerization, a facile surface modification technique, was examined as an approach to reduce bacterial deposition onto RO membranes and thus contribute to mitigation of biofouling. For this purpose an RO membrane ESPA-1 was surface-grafted with a zwitterionic and negatively and positively charged monomers. The low monomer concentrations and low degrees of grafting employed in modifications moderately reduced flux (by 20-40%) and did not affect salt rejection, yet produced substantial changes in surface chemistry, charge and hydrophilicity. The propensity to bacterial attachment of original and modified membranes was assessed using bacterial deposition tests carried out in a parallel plate flow setup using a fluorescent strain of Pseudomonas fluorescens. Compared to unmodified ESPA-1 the deposition (mass transfer) coefficient was significantly increased for modification with the positively charged monomer. On the other hand, a substantial reduction in bacterial deposition rates was observed for membranes modified with zwitterionic monomer and, still more, with very hydrophilic negatively charged monomers. This trend is well explained by the effects of surface charge (as measured by ζ-potential) and hydrophilicity (contact angle). It also well correlated with force distance measurements by AFM using surrogate spherical probes with a negative surface charge mimicking the bacterial surface. The positively charged surface showed a strong hysteresis with a large adhesion force, which was weaker for unmodified ESPA-1 and still weaker for zwitterionic surface, while negatively charged surface showed a long-range repulsion and negligible hysteresis. These results demonstrate the potential of using the proposed surface- modification approach for varying surface characteristics, charge and hydrophilicity, and thus minimizing bacterial deposition and potentially reducing propensity biofouling.