23 research outputs found

    Low-Temperature Photochemically Activated Amorphous Indium-Gallium-Zinc Oxide for Highly Stable Room-Temperature Gas Sensors

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    We report on highly stable amorphous indium-gallium-zinc oxide (IGZO) gas sensors for ultraviolet (UV)-activated room-temperature detection of volatile organic compounds (VOCs). The IGZO sensors fabricated by a low-temperature photochemical activation process and exhibiting two orders higher photocurrent compared to conventional zinc oxide sensors, allowed high gas sensitivity against various VOCs even at room temperature. From a systematic analysis, it was found that by increasing the UV intensity, the gas sensitivity, response time, and recovery behavior of an IGZO sensor were strongly enhanced. In particular, under an UV intensity of 30 mW cm<sup>–2</sup>, the IGZO sensor exhibited gas sensitivity, response time and recovery time of 37%, 37 and 53 s, respectively, against 750 ppm concentration of acetone gas. Moreover, the IGZO gas sensor had an excellent long-term stability showing around 6% variation in gas sensitivity over 70 days. These results strongly support a conclusion that a low-temperature solution-processed amorphous IGZO film can serve as a good candidate for room-temperature VOCs sensors for emerging wearable electronics

    High-Mobility and Hysteresis-Free Flexible Oxide Thin-Film Transistors and Circuits by Using Bilayer Sol–Gel Gate Dielectrics

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    In this paper, we demonstrate high-performance and hysteresis-free solution-processed indium–gallium–zinc oxide (IGZO) thin-film transistors (TFTs) and high-frequency-operating seven-stage ring oscillators using a low-temperature photochemically activated Al<sub>2</sub>O<sub>3</sub>/ZrO<sub>2</sub> bilayer gate dielectric. It was found that the IGZO TFTs with single-layer gate dielectrics such as Al<sub>2</sub>O<sub>3</sub>, ZrO<sub>2</sub>, or sodium-doped Al<sub>2</sub>O<sub>3</sub> exhibited large hysteresis, low field-effect mobility, or unstable device operation owing to the interfacial/bulk trap states, insufficient band offset, or a substantial number of mobile ions present in the gate dielectric layer, respectively. To resolve these issues and to explain the underlying physical mechanisms, a series of electrical analyses for various single- and bilayer gate dielectrics was carried out. It is shown that compared to single-layer gate dielectrics, the Al<sub>2</sub>O<sub>3</sub>/ZrO<sub>2</sub> gate dielectric exhibited a high dielectric constant of 8.53, low leakage current density (∼10<sup>–9</sup> A cm<sup>–2</sup> at 1 MV cm<sup>–1</sup>), and stable operation at high frequencies. Using the photochemically activated Al<sub>2</sub>O<sub>3</sub>/ZrO<sub>2</sub> gate dielectric, the seven-stage ring oscillators operating at an oscillation frequency of ∼334 kHz with a propagation delay of <216 ns per stage were successfully demonstrated on a polymeric substrate

    Static and Dynamic Water Motion-Induced Instability in Oxide Thin-Film Transistors and Its Suppression by Using Low‑<i>k</i> Fluoropolymer Passivation

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    Here, we report static and dynamic water motion-induced instability in indium–gallium–zinc-oxide (IGZO) thin-film transistors (TFTs) and its effective suppression with the use of a simple, solution-processed low-<i>k</i> (ε ∼ 1.9) fluoroplastic resin (FPR) passivation layer. The liquid-contact electrification effect, in which an undesirable drain current modulation is induced by a dynamic motion of a charged liquid such as water, can cause a significant instability in IGZO TFTs. It was found that by adopting a thin (∼44 nm) FPR passivation layer for IGZO TFTs, the current modulation induced by the water-contact electrification was greatly reduced in both off- and on-states of the device. In addition, the FPR-passivated IGZO TFTs exhibited an excellent stability to static water exposure (a threshold voltage shift of +0.8 V upon 3600 s of water soaking), which is attributed to the hydrophobicity of the FPR passivation layer. Here, we discuss the origin of the current instability caused by the liquid-contact electrification as well as various static and dynamic stability tests for IGZO TFTs. On the basis of our findings, we believe that the use of a thin, solution-processed FPR passivation layer is effective in suppressing the static and dynamic water motion-induced instabilities, which may enable the realization of high-performance and environment-stable oxide TFTs for emerging wearable and skin-like electronics

    Synthesis of Vertical MoO<sub>2</sub>/MoS<sub>2</sub> Core–Shell Structures on an Amorphous Substrate via Chemical Vapor Deposition

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    Vertical MoO<sub>2</sub>/MoS<sub>2</sub> core–shell structures were synthesized on an amorphous surface (SiO<sub>2</sub>) by chemical vapor deposition at a high heating rate using a configuration in which the vapor phase was confined. The confined reaction configuration was achieved by partially covering the MoO<sub>3</sub>-containing boat with a substrate, which allowed rapid buildup of the partially reduced MoO<sub>3–<i>x</i></sub> crystals in an early stage (below 680 °C). Rapid temperature ramping to 780 °C enabled spontaneous transition of the reaction environment from sulfur-poor to sulfur-rich, which induced a sequential phase transition from MoO<sub>3–<i>x</i></sub> to intermediate MoO<sub>2</sub> and finally to MoO<sub>2</sub>/MoS<sub>2</sub> core–shell structures. The orthorhombic crystal structure of MoO<sub>3–<i>x</i></sub> contributed to the formation of vertical crystals on the amorphous substrate, whereas the nonvolatility of the subsequently formed MoO<sub>2</sub> enabled layer-by-layer sulfurization to form MoS<sub>2</sub> on the oxide surface with minimal resublimation loss of MoO<sub>2</sub>. By adjustment of the sulfurization temperature and time, excellent control over the thickness of the MoS<sub>2</sub> shell was achieved through the proposed synthesis method

    Ultrasensitive Room-Temperature Operable Gas Sensors Using p‑Type Na:ZnO Nanoflowers for Diabetes Detection

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    Ultrasensitive room-temperature operable gas sensors utilizing the photocatalytic activity of Na-doped p-type ZnO (Na:ZnO) nanoflowers (NFs) are demonstrated as a promising candidate for diabetes detection. The flowerlike Na:ZnO nanoparticles possessing ultrathin hierarchical nanosheets were synthesized by a facile solution route at a low processing temperature of 40 °C. It was found that the Na element acting as a p-type dopant was successfully incorporated in the ZnO lattice. On the basis of the synthesized p-type Na:ZnO NFs, room-temperature operable chemiresistive-type gas sensors were realized, activated by ultraviolet (UV) illumination. The Na:ZnO NF gas sensors exhibited high gas response (<i>S</i> of 3.35) and fast response time (∼18 s) and recovery time (∼63 s) to acetone gas (100 ppm, UV intensity of 5 mW cm<sup>–2</sup>), and furthermore, subppm level (0.2 ppm) detection was achieved at room temperature, which enables the diagnosis of various diseases including diabetes from exhaled breath

    Monolithic Metal Oxide Transistors

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    We devised a simple transparent metal oxide thin film transistor architecture composed of only two component materials, an amorphous metal oxide and ion gel gate dielectric, which could be entirely assembled using room-temperature processes on a plastic substrate. The geometry cleverly takes advantage of the unique characteristics of the two components. An oxide layer is metallized upon exposure to plasma, leading to the formation of a monolithic source–channel–drain oxide layer, and the ion gel gate dielectric is used to gate the transistor channel effectively at low voltages through a coplanar gate. We confirmed that the method is generally applicable to a variety of sol–gel-processed amorphous metal oxides, including indium oxide, indium zinc oxide, and indium gallium zinc oxide. An inverter NOT logic device was assembled using the resulting devices as a proof of concept demonstration of the applicability of the devices to logic circuits. The favorable characteristics of these devices, including (i) the simplicity of the device structure with only two components, (ii) the benign fabrication processes at room temperature, (iii) the low-voltage operation under 2 V, and (iv) the excellent and stable electrical performances, together support the application of these devices to low-cost portable gadgets, <i>i.e</i>., cheap electronics

    Insight into the Microenvironments of the Metal–Ionic Liquid Interface during Electrochemical CO<sub>2</sub> Reduction

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    Recently, many experimental and theoretical efforts are being intensified to develop high-performance catalysts for electrochemical CO<sub>2</sub> conversion. Beyond the catalyst material screening, it is also critical to optimize the surrounding reaction medium. From vast experiments, inclusion of room-temperature ionic liquid (RTIL) in the electrolyte is found to be beneficial for CO<sub>2</sub> conversion; however, there is no unified picture of the role of RTIL, prohibiting further optimization of the reaction medium. Using a state-of-the-art multiscale simulation, we here unveil the atomic origin of the catalytic promotion effect of RTIL during CO<sub>2</sub> conversion. Unlike the conventional belief, which assumes a specific intermolecular coordination by the RTIL component, we find that the promotion effect is collectively manifested by tuning the reaction microenvironment. This mechanism suggests the critical importance of the bulk properties (e.g., resistance, gas solubility and diffusivity, viscosity, etc.) over the detailed chemical variations of the RTIL components in designing the optimal electrolyte components, which is further supported by our experiments. This fundamental understanding of complex electrochemical interfaces will help in the development of more advanced electrochemical CO<sub>2</sub> conversion catalytic systems in the future

    Low-Temperature Postfunctionalization of Highly Conductive Oxide Thin-Films toward Solution-Based Large-Scale Electronics

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    Although transparent conducting oxides (TCOs) have played a key role in a wide range of solid-state electronics from conventional optoelectronics to emerging electronic systems, the processing temperature and conductivity of solution-processed materials seem to be far exceeding the thermal limitations of soft materials and insufficient for high-perfomance large-area systems, respectively. Here, we report a strategy to form highly conductive and scalable solution-processed oxide materials and their successful translation into large-area electronic applications, which is enabled by photoassisted postfunctionalization at low temperature. The low-temperature fabrication of indium–tin-oxide (ITO) thin films was achieved by using photoignited combustion synthesis combined with photoassisted reduction process under hydrogen atmosphere. It was noteworthy that the photochemically activated hydrogens on ITO surface could be triggered to facilitate highly crystalline oxygen deficient structure allowing significant increase of carrier concentration and mobility through film microstructure modifications. The low-temperature postfunctionalized ITO films demonstrated conductivity of >1607 S/cm and sheet resistance of <104 Ω/□ under the process temperature of less than 300 °C, which are comparable to those of vacuum-deposited and high-temperature annealed ITO films. Based on the photoassisted postfunctionalization route, all-solution-processed transparent metal-oxide thin-film-transistors and large-area integrated circuits with the ITO bus lines were demonstrated, showing field-effect mobilities of >6.5 cm<sup>2</sup> V<sup>–1</sup> s<sup>–1</sup> with relatively good operational stability and oscillation frequency of more than 1 MHz in 7-stage ring oscillators, respectively

    Highly Sensitive Textile Strain Sensors and Wireless User-Interface Devices Using All-Polymeric Conducting Fibers

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    Emulation of diverse electronic devices on textile platform is considered as a promising approach for implementing wearable smart electronics. Of particular, the development of multifunctional polymeric fibers and their integration in common fabrics have been extensively researched for human friendly wearable platforms. Here we report a successful emulation of multifunctional body-motion sensors and user-interface (UI) devices in textile platform by using in situ polymerized poly­(3,4-ethylenedioxythiophene) (PEDOT)-coated fibers. With the integration of PEDOT fibers in a fabric, via an optimization of the fiber pattern design, multifunctional textile sensors such as highly sensitive and reliable strain sensors (with maximum gauge factor of ∼1), body-motion monitoring sensors, touch sensors, and multilevel strain recognition UI devices were successfully emulated. We demonstrate the facile utilization of the textile-based multifunctional sensors and UI devices by implementing in a wireless system that is capable of expressing American Sign Language through predefined hand gestures

    Transcriptional regulation of bile acid enzyme genes by <i>Crebh.</i>

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    <p>(<b>A</b>) Mice (n = 5) or primary human hepatocytes (n = 3) were infected with indicated adenoviruses for 96 hrs. Liver tissues were obtained and protein and total RNA was extracted for western blot and qPCR analyses, respectively. *<i>p</i><0.05 vs. Ad-GFP group. (<b>B</b>) HepG2 cells were co-transfected with CREBH-N and different CYP7A1-Luc and CYP27A1-Luc promoter constructs, and luciferase assay was performed. (<b>C–D</b>) HepG2 cells were transfected with wild type (wt) or CREBH-mutant (mut) constructs of CYP7A1-Luc or CYP27A1-Luc followed by 2-AG-ether treatment for 12 hrs and luciferase assay was performed (D) or immunoprecipitation of HepG2 chromatin from cells exposed to DMSO (control) or 2-AG-ether was performed with IgG or Crebh antibody (E). Promoter regions were amplified by PCR, as depicted. Percentage of DNA immunoprecipitated with Crebh antibody relative to input chromatin was quantified by qPCR. *<i>p</i><0.05 vs. control. Data represents mean ± SE.</p
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