Always cite the published version, so the author(s) will receive recognition through services that track citation counts, e.g. Scopus. If you need to cite the page number of the author manuscript from TSpace because you cannot access the published version, then cite the TSpace version in addition to the published version using the permanent URI (handle) found on the record page. Abstract. Thermoelectric effect is defined as the revisable translation between thermal and electrical energy. In this paper, we investigate the properties of p-type poly(vinylidene fluoride) (PVDF) based polymer composite foams that can be used in next generation energy harvesting applications. The composites were created via continuous melt blending method. Multi-walled carbon nanotubes (MWCNTs) and graphene nano-platelets (GNPs) were used as secondary phases to strengthen the electrical conductivity of the composites. Foam structures were later generated via super-critical carbon dioxide saturation method. We study the material properties between solid and foam samples; the results indicate a dramatic increase in overall thermoelectric properties for GNP foamed samples. We also report at least an order decreased in thermal conductivity which is in favor of thermoelectric effect. An unexpected drop in electrical conductivity was observed after the foaming process and can be explained by large volumetric expansion of the foam. Finally we report the Seebeck coefficient for both types of composite foams: 11 μV/K for 5 wt% MWCNT/PVDF foam and 58 μV/K for 15 wt% GNP/PVDF foam. IntroductionThermoelectric (TE) effect is known as the direct conversion between electrical and thermal energy and such effect can be explained by three different phenomena: Seebeck effect, Peliter effect, and Thomson effect. When a temperature gradient is applied to a circuit that consists of two different electric conductors, a small current can be observed which is called the Seebeck effect. The opposite phenomenon is called the Peliter effect, of which the junctions of the two conductors may either absorb or release heat when a voltage is supplied to the circuit. Lastly, the Thomson Effect states that when an electric current is passing through a conductor, certain amount of heat (Thomson heat) would be released or absorbed by the material and such heat is does not include the non-reversible Joule heating which is generated from the electric resistance nature of the material [1]. Seebeck effect is currently being implemented in verity types of temperature sensors or thermocouples [2] while the Peliter effect can be applied in different types of heat engines and coolers [3]. Other than temperature sensors, Seebeck effect also being widely researched for energy harvesting

Overcoming the inhibitory effects of excess environmental ammonium on nitrogenase synthesis or activity and preventing ammonium assimilation have been considered strategies to increase the amount of fixed nitrogen transferred from bacterial to plant partners in associative or symbiotic plant-diazotroph relationships. The GlnE adenylyltransferase/adenylyl-removing enzyme catalyzes reversible adenylylation of glutamine synthetase (GS), thereby affecting the posttranslational regulation of ammonium assimilation that is critical for the appropriate coordination of carbon and nitrogen assimilation. Since GS is key to the sole ammonium assimilation pathway of Azotobacter vinelandii, attempts to obtain deletion mutants in the gene encoding GS (glnA) have been unsuccessful. We have generated a glnE deletion strain, thus preventing posttranslational regulation of GS. The resultant strain containing constitutively active GS is unable to grow well on ammonium-containing medium, as previously observed in other organisms, and can be cultured only at low ammonium concentrations. This phenotype is caused by the lack of downregulation of GS activity, resulting in high intracellular glutamine levels and severe perturbation of the ratio of glutamine to 2-oxoglutarate under excess-nitrogen conditions. Interestingly, the mutant can grow diazotrophically at rates comparable to those of the wild type. This observation suggests that the control of nitrogen fixation-specific gene expression at the transcriptional level in response to 2-oxoglutarate via NifA is sufficiently tight to alone regulate ammonium production at levels appropriate for optimal carbon and nitrogen balance.IMPORTANCE In this study, the characterization of the glnE knockout mutant of the model diazotroph Azotobacter vinelandii provides significant insights into the integration of the regulatory mechanisms of ammonium production and ammonium assimilation during nitrogen fixation. The work reveals the profound fidelity of nitrogen fixation regulation in providing ammonium sufficient for maximal growth but constraining energetically costly excess production. A detailed fundamental understanding of the interplay between the regulation of ammonium production and assimilation is of paramount importance in exploiting existing and potentially engineering new plant-diazotroph relationships for improved agriculture.KEYWORDS Azotobacter vinelandii, glnE, ammonium assimilation, nitrogen fixation, regulation, glutamine synthetase T he most common pathways of ammonium assimilation in bacteria are known to be mediated by two major pathways (1, 2): the glutamate dehydrogenase (GDH) pathway when the extracellular concentration of ammonium is high, and the glutamine synthetase (GS) and glutamate synthase (GOGAT) pathway at low ammonium concentrations. In addition, the alanine dehydrogenase (ADH) enzyme has also been suggested to be involved in ammonium assimilation in most methylotrophs (3). The GDH

In this study, we develop a Na +-sensitive thin-film transistor (TFT) for a biocompatible ion sensor and investigate its cytotoxicity. A transparent amorphous oxide semiconductor composed of amorphous In-Ga-Zn-oxide (a-InGaZnO) is utilized as a channel of the Na +-sensitive TFT, which includes an indium tin oxide (ITO) film as the source and drain electrodes and a Ta 2 O 5 thin-film gate, onto which a Na +-sensitive membrane is coated. As one of the Na +sensitive membranes, the polyvinyl chloride (PVC) membrane with bis(12-crown-4) as the ionophore used on the TFT sensors shows good sensitivity and selectivity to changes in Na + concentration but has high cytotoxicity owing to the leaching of its plasticizer to the solution; the plasticizer is added to solve and entrap the ionophore in the PVC membrane. On the other hand, a plasticizer-free Na +-sensitive membrane, the fluoropolysilicone (FPS) membrane with the bis(12-crown-4) ionophore, also reduces cell viability owing to the leaching of the ionophore. However, the FPS membrane with calix[4]arene as the ionophore on the gate of TFT sensors exhibits not only favorable electrical properties but also the lack of cytotoxicity. Thus, considering structural flexibility of TFTs, a platform based on TFT sensors coated with the Na +-sensitive FPS membrane containing calix[4]arene is suitable as a biocompatible Na + sensing system for the continuous monitoring of ionic components in biological fluids such as sweat and tears.

Nanowire-based field-effect transistors (FETs) have demonstrated considerable promise for a new generation of chemical and biological sensors. Indium arsenide (InAs), by virtue of its high electron mobility and intrinsic surface accumulation layer of electrons, holds properties beneficial for creating high performance sensors that can be used in applications such as point-of-care testing for patients diagnosed with chronic diseases. Here, we propose devices based on a parallel configuration of InAs nanowires and investigate sensor responses from measurements of conductance over time and FET characteristics. The devices were tested in controlled concentrations of vapour containing acetic acid, 2-butanone and methanol. After adsorption of analyte molecules, trends in the transient current and transfer curves are correlated with the nature of the surface interaction. Specifically, we observed proportionality between acetic acid concentration and relative conductance change, off current and surface charge density extracted from subthreshold behaviour. We suggest the origin of the sensing response to acetic acid as a two-part, reversible acid-base and redox reaction between acetic acid, InAs and its native oxide that forms slow, donor-like states at the nanowire surface. We further describe a simple model that is able to distinguish the occurrence of physical versus chemical adsorption by comparing the values of the extracted surface charge density. These studies demonstrate that InAs nanowires can produce a multitude of sensor responses for the purpose of developing next generation, multi-dimensional sensor applications.

Much recent attention has been focused on the development of field-effect transistors based on low-dimensional nanostructures for the detection and manipulation of molecules. Because of their extraordinarily high charge sensitivity, InAs nanowires present an excellent material system in which to probe and study the behavior of molecules on their surfaces and elucidate the underlying mechanisms dictating the sensor response. So far, chemical sensors have relied on slow, activated processes restricting their applicability to high temperatures and macroscopic adsorbate coverages. Here, we identify the transition into a highly sensitive regime of chemical sensing at ultralow concentrations (<1 ppm) via physisorption at room temperature using field-effect transistors with channels composed of several thousand InAs nanowires and ethanol as a simple analyte molecule. In this regime, the nanowire conductivity is dictated by a local gating effect from individual dipoles, leading to a nonlinear enhancement of the sensitivity. At higher concentrations (>1 ppm), the nanowire channel is globally gated by a uniform dipole layer at the nanowire surface. The former leads to a dramatic increase in sensitivity due to weakened screening and the one-dimensional geometry of the nanowire. In this regime, we detect concentrations of ethanol vapor as low as 10 ppb, 100 times below the lowest concentrations previously reported. Furthermore, we demonstrate electrostatic control of the sensitivity and dynamic range of the InAs nanowire-based sensor and construct a unified model that accurately describes and predicts the sensor response over the tested concentration range (10 ppb to 10 ppm).