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Sökning: WFRF:(Ouyang Liangqi)

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1.
  • Ajjan, Fátima, et al. (författare)
  • Scalable Asymmetric Supercapacitors Based on Hybrid Organic/Biopolymer Electrodes
  • 2017
  • Ingår i: ADVANCED SUSTAINABLE SYSTEMS. - : WILEY-V C H VERLAG GMBH. - 2366-7486. ; 1:8
  • Tidskriftsartikel (refereegranskat)abstract
    • A trihybrid bioelectrode composed of lignin, poly(3,4-ethylenedioxythiophene) (PEDOT), and poly(aminoanthraquinone) (PAAQ) is prepared by a two-step galvanostatic electropolymerization, and characterized for supercapacitor applications. Using PEDOT/Lignin as a base layer, followed by the consecutive deposition of PAAQ, the hybrid electrode PEDOT/Lignin/PAAQ shows a high specific capacitance of 418 F g(-1) with small self-discharge. This trihybrid electrode material can be assembled into symmetric and asymmetric super-capacitors. The asymmetric supercapacitor uses PEDOT + Lignin/PAAQ as positive electrode and PEDOT/PAAQ as negative electrode, and exhibits superior electrochemical performance due to the synergistic effect of the two electrodes, which leads to a specific capacitance of 74 F g(-1). It can be reversibly cycled in the voltage range of 0-0.7 V. More than 80% capacitance is retained after 10 000 cycles. These remarkable features reveal the exciting potential of a full organic energy storage device with long cycle life.
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2.
  • Elfwing, Anders, et al. (författare)
  • Conducting Helical Structures from Celery Decorated with a Metallic Conjugated Polymer Give Resonances in the Terahertz Range
  • 2018
  • Ingår i: Advanced Functional Materials. - : WILEY-V C H VERLAG GMBH. - 1616-301X .- 1616-3028. ; 28:24
  • Tidskriftsartikel (refereegranskat)abstract
    • A method to decorate cellulose-based helices retrieved from the plant celery with a conductive polymer is proposed. Using a layer-by-layer method, the decoration of the polyanionic conducting polymer poly(4-(2,3-dihydrothieno [3,4-b]-[1,4]dioxin-2-yl-methoxy)-1-butanesulfonic acid (PEDOT-S) is enhanced after coating the negatively charged cellulose helix with a polycationic polyethyleneimine. Microscopy techniques and two-point probe are used to image the structure and measure the conductivity of the helix. Analysis of the optical and electrical properties of the coated helix in the terahertz (THz) frequency range shows a resonance close to 1 THz and a broad shoulder that extends to 3.5 THz, consistent with electromagnetic models. Moreover, as helical antennas, it is shown that both axial and normal modes are present, which are correlated to the orientation and antenna electrical lengths of the coated helices. This work opens the possibility of designing tunable terahertz antennas through simple control of their dimensions and orientation.
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3.
  • Elfwing, Anders, et al. (författare)
  • DNA Based Hybrid Material for Interface Engineering in Polymer Solar Cells
  • 2018
  • Ingår i: ACS Applied Materials and Interfaces. - : AMER CHEMICAL SOC. - 1944-8244 .- 1944-8252. ; 10:11, s. 9579-9586
  • Tidskriftsartikel (refereegranskat)abstract
    • A new solution processable electron transport material (ETM) is introduced for use in photovoltaic devices, which consists of a metallic conjugated polyelectrolyte, poly(4-(2,3-dihydrothieno[3,4-b]-[1,4]dioxin-2-yl-methoxy)-1-butanesulfonic acid (PEDOT-S), and surfactant-functionalized deoxyribonucleic acid (DNA) (named DNA:CTMA:PEDOT-S). This ETM is demonstrated to effectively work for bulk-heterojunction organic photovoltaic devices (OPV) based on different electron acceptor materials. The fill factor, the open circuit voltage, and the overall power conversion efficiency of the solar cells with a DNA:CTMA:PEDOT-S modified cathode are comparable to those of devices with a traditional lithium fluoride/aluminum cathode. The new electron transport layer has high optical transmittance, desired work function and selective electron transport. A dipole effect induced by the use of the surfactant cetyltrimethylammonium chloride (CTMA) is responsible for lowering the electrode work function. The DNA:CTMA complex works as an optical absorption dilutor, while PEDOT-S provides the conducting pathway for electron transport, and allows thicker layer to be used, enabling printing. This materials design opens a new pathway to harness and optimize the electronic and optical properties of printable interface materials.
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4.
  • Ever Aguirre, Luis, et al. (författare)
  • Diatom frustules protect DNA from ultraviolet light
  • 2018
  • Ingår i: Scientific Reports. - : Springer Science and Business Media LLC. - 2045-2322. ; 8:1
  • Tidskriftsartikel (refereegranskat)abstract
    • The evolutionary causes for generation of nano and microstructured silica by photosynthetic algae are not yet deciphered. Diatoms are single photosynthetic algal cells populating the oceans and waters around the globe. They generate a considerable fraction (20-30%) of all oxygen from photosynthesis, and 45% of total primary production of organic material in the sea. There are more than 100,000 species of diatoms, classified by the shape of the glass cage in which they live, and which they build during algal growth. These glass structures have accumulated for the last 100 million of years, and left rich deposits of nano/microstructured silicon oxide in the form of diatomaceous earth around the globe. Here we show that reflection of ultraviolet light by nanostructured silica can protect the deoxyribonucleic acid (DNA) in the algal cells, and that this may be an evolutionary cause for the formation of glass cages. © 2018 The Author(s).
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5.
  • Khaliliazar, Shirin, et al. (författare)
  • Electrochemical Detection of Genomic DNA Utilizing Recombinase Polymerase Amplification and Stem-Loop Probe
  • 2020
  • Ingår i: ACS Omega. - : AMER CHEMICAL SOC. - 2470-1343. ; 5:21, s. 12103-12109
  • Tidskriftsartikel (refereegranskat)abstract
    • Nucleic acid tests integrated into digital point-of-care (POC) diagnostic systems have great potential for the future of health care. However, current methods of DNA amplification and detection require bulky and expensive equipment, many steps, and long process times, which complicate their integration into POC devices. We have combined an isothermal DNA amplification method, recombinase polymerase amplification, with an electrochemical stem-loop (S-L) probe DNA detection technique. By combining these methods, we have created a system that is able to specifically amplify and detect as few as 10 copies/mu L Staphylococcus epidermidis DNA with a total time to result of 70-75 min.
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6.
  • Khaliliazar, Shirin, et al. (författare)
  • Woven Electroanalytical Biosensor for Nucleic AcidAmplification Tests
  • 2021
  • Ingår i: Advanced Healthcare Materials. - : Wiley-VCH Verlagsgesellschaft. - 2192-2640 .- 2192-2659. ; 10:11, s. 2100034-
  • Tidskriftsartikel (refereegranskat)abstract
    • Fiber-based biosensors enable a new approach in analytical diagnosticdevices. The majority of textile-based biosensors, however, rely oncolorimetric detection. Here a woven biosensor that integrates microfluidicsstructures in combination with an electroanalytical readout based on athiol-self-assembled monolayer (SAM) for Nucleic Acid Amplification Testing,NAATs is shown. Two types of fiber-based electrodes are systematicallycharacterized: pure gold microwires (bond wire) and off-the-shelf plasmagold-coated polyester multifilament threads to evaluate their potential to formSAMs on their surface and their electrochemical performance in woven textile.A woven electrochemical DNA (E-DNA) sensor using a SAM-based stem-loopprobe-modified gold microwire is fabricated. These sensors can specificallydetect unpurified, isothermally amplified genomic DNA of Staphylococcusepidermidis (10 copies/μL) by recombinase polymerase amplification (RPA).This work demonstrates that textile-based biosensors have the potential forintegrating and being employed as automated, sample-to-answer analyticaldevices for point-of-care (POC) diagnostics.
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7.
  • Müller, Christian, 1980, et al. (författare)
  • From Single Molecules to Thin Film Electronics, Nanofibers, e-Textiles and Power Cables : Bridging Length Scales with Organic Semiconductors
  • 2019
  • Ingår i: Advanced Materials. - : Wiley-VCH Verlag. - 0935-9648 .- 1521-4095.
  • Tidskriftsartikel (refereegranskat)abstract
    • Organic semiconductors are the centerpiece of several vibrant research fields from single-molecule to organic electronics, and they are finding increasing use in bioelectronics and even classical polymer technology. The versatile chemistry and broad range of electronic functionalities of conjugated materials enable the bridging of length scales 15 orders of magnitude apart, ranging from a single nanometer (10 −9 m) to the size of continents (10 6 m). This work provides a taste of the diverse applications that can be realized with organic semiconductors. The reader will embark on a journey from single molecular junctions to thin film organic electronics, supramolecular assemblies, biomaterials such as amyloid fibrils and nanofibrillated cellulose, conducting fibers and yarns for e-textiles, and finally to power cables that shuffle power across thousands of kilometers.
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8.
  • Musumeci, Chiara, et al. (författare)
  • Organic electrochemical transistors from supramolecular complexes of conjugated polyelectrolyte PEDOTS
  • 2019
  • Ingår i: Journal of Materials Chemistry C. - : ROYAL SOC CHEMISTRY. - 2050-7526 .- 2050-7534. ; 7:10, s. 2987-2993
  • Tidskriftsartikel (refereegranskat)abstract
    • Counterion exchange strategies are used to modify the hydrophilic character of the self-doped conjugated polyelectrolyte PEDOTS. The supramolecular complexes, soluble in organic solvents, are suitable to fabricate finely performing thin active layers in organic electrochemical transistors (OECTs). We demonstrate that ionic transport in these PEDOTS based complexes, thus their performance in OECT devices, is governed by a delicate balance among degree of doping, wettability and porosity, which can be controlled by a precise tuning of the polyelectrolyte/hydrophobic counterion ratio. We also show that the device operation can be modulated by varying the composition of the aqueous electrolyte in a range compatible with biological processes, making these materials suitable candidates to be interfaced with living cells.
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9.
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10.
  • Ouyang, Liangqi, et al. (författare)
  • Enhanced PEDOT adhesion on solid substrates with electrografted P(EDOT-NH2)
  • 2017
  • Ingår i: Science Advances. - : American Association for the Advancement of Science. - 2375-2548. ; 3:3
  • Tidskriftsartikel (refereegranskat)abstract
    • Conjugated polymers, such as poly(3,4-ethylene dioxythiophene) (PEDOT), have emerged as promising materials for interfacing biomedical devices with tissue because of their relatively soft mechanical properties, versatile organic chemistry, and inherent ability to conduct both ions and electrons. However, their limited adhesion to substrates is a concern for in vivo applications. We report an electrografting method to create covalently bonded PEDOT on solid substrates. An amine-functionalized EDOT derivative (2,3-dihydrothieno[3,4-b][1,4]dioxin-2-yl)methanamine (EDOT-NH2), was synthesized and then electrografted onto conducting substrates including platinum, iridium, and indium tin oxide. The electrografting process was performed under slightly basic conditions with an overpotential of ~2 to 3 V. A nonconjugated, cross-linked, and well-adherent P(EDOT-NH2)–based polymer coating was obtained. We found that the P(EDOT-NH2) polymer coating did not block the charge transport through the interface. Subsequent PEDOT electrochemical deposition onto P(EDOT-NH2)–modified electrodes showed comparable electroactivity to pristine PEDOT coating. With P(EDOT-NH2) as an anchoring layer, PEDOT coating showed greatly enhanced adhesion. The modified coating could withstand extensive ultrasonication (1 hour) without significant cracking or delamination, whereas PEDOT typically delaminated after seconds of sonication. Therefore, this is an effective means to selectively modify microelectrodes with highly adherent and highly conductive polymer coatings as direct neural interfaces. © 2017 The Authors, some rights reserved.
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