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Open AccessLetter Switchable Two-Dimensional Liquid Crystal Grating in Blue Phase
Crystals 2017, 7(6), 182; doi:10.3390/cryst7060182
Received: 11 May 2017 / Revised: 18 June 2017 / Accepted: 19 June 2017 / Published: 21 June 2017
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Abstract
We demonstrate a switchable two-dimensional phase grating in blue phase liquid crystal (BPLC), which is fabricated by sawtooth in-plane-switch (IPS) electrodes. They are used to generate the horizontal electric field on a single indium-tin-oxide (ITO) glass substrate and, as a result, the 1-D
[...] Read more.
We demonstrate a switchable two-dimensional phase grating in blue phase liquid crystal (BPLC), which is fabricated by sawtooth in-plane-switch (IPS) electrodes. They are used to generate the horizontal electric field on a single indium-tin-oxide (ITO) glass substrate and, as a result, the 1-D and 2-D phase gratings can be mutual switched via different polarizations of incident light with an applied voltage. The first-order diffraction efficiency is up to 20% and 10% for the 1-D and 2-D phase grating at V = 150 V, respectively. Moreover, the rise and decay time is 0.9 and 1.1 ms, respectively, which is suitable for wide applications of high-speed optical manipulations. Full article
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Open AccessArticle Development of a Novel Transparent Flexible Capacitive Micromachined Ultrasonic Transducer
Sensors 2017, 17(6), 1443; doi:10.3390/s17061443
Received: 27 April 2017 / Revised: 5 June 2017 / Accepted: 15 June 2017 / Published: 20 June 2017
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Abstract
This paper presents the world’s first transparent flexible capacitive micromachined ultrasonic transducer (CMUT) that was fabricated through a roll-lamination technique. This polymer-based CMUT has advantages of transparency, flexibility, and non-contacting detection which provide unique functions in display panel applications. Comprising an indium tin
[...] Read more.
This paper presents the world’s first transparent flexible capacitive micromachined ultrasonic transducer (CMUT) that was fabricated through a roll-lamination technique. This polymer-based CMUT has advantages of transparency, flexibility, and non-contacting detection which provide unique functions in display panel applications. Comprising an indium tin oxide-polyethylene terephthalate (ITO-PET) substrate, SU-8 sidewall and vibrating membranes, and silver nanowire transparent electrode, the transducer has visible-light transmittance exceeding 80% and can operate on curved surfaces with a 40 mm radius of curvature. Unlike the traditional silicon-based high temperature process, the CMUT can be fabricated on a flexible substrate at a temperature below 100 °C to reduce residual stress introduced at high temperature. The CMUT on the curved surfaces can detect a flat target and finger at distances up to 50 mm and 40 mm, respectively. The transparent flexible CMUT provides a better human-machine interface than existing touch panels because it can be integrated with a display panel for non-contacting control in a health conscious environment and the flexible feature is critical for curved display and wearable electronics. Full article
(This article belongs to the Section Physical Sensors)
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Open AccessArticle Study of ZnS Nanostructures Based Electrochemical and Photoelectrochemical Biosensors for Uric Acid Detection
Sensors 2017, 17(6), 1235; doi:10.3390/s17061235
Received: 15 April 2017 / Revised: 14 May 2017 / Accepted: 18 May 2017 / Published: 28 May 2017
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Abstract
Uric acid (UA) is a kind of purine metabolism product and important in clinical diagnosis. In this work, we present a study of ZnS nanostructures-based electrochemical and photoelectrochemical biosensors for UA detection. Through a simple hydrothermal method and varying the ratio of reaction
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Uric acid (UA) is a kind of purine metabolism product and important in clinical diagnosis. In this work, we present a study of ZnS nanostructures-based electrochemical and photoelectrochemical biosensors for UA detection. Through a simple hydrothermal method and varying the ratio of reaction solvents, we obtained ZnS nanomaterials of one-dimensional to three-dimensional morphologies and they were characterized using field emission scanning electron microscopy (FESEM) and X-ray diffraction (XRD). To fabricate the UA biosensor and study the effect of material morphology on its performance, ZnS nanomaterials were deposited on indium tin oxide (ITO) conducting glass and then coated with uricase by physical absorption. Three kinds of working electrodes were characterized by cyclic voltammetry method. The effect of material morphology on performance of UA detection was investigated via amperometric response based electrochemical method based on enzymatic reaction. The ZnS urchin-like nanostructures electrode shows better sensitivity compared with those made of nanoparticles and nanoflakes because of its high surface-area-to-volume ratio. The photoelectrochemical method for detection of UA was also studied. The sensitivity was increased 5 times after irradiation of 300 nm UV light. These results indicate that ZnS nanostructures are good candidate materials for developing enzyme-based UA biosensors. Full article
(This article belongs to the Section Biosensors)
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Open AccessArticle Transparent Electrodes Based on Silver Nanowire Networks: From Physical Considerations towards Device Integration
Materials 2017, 10(6), 570; doi:10.3390/ma10060570
Received: 2 February 2017 / Revised: 13 May 2017 / Accepted: 16 May 2017 / Published: 24 May 2017
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Abstract
The past few years have seen a considerable amount of research devoted to nanostructured transparent conducting materials (TCM), which play a pivotal role in many modern devices such as solar cells, flexible light-emitting devices, touch screens, electromagnetic devices, and flexible transparent thin film
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The past few years have seen a considerable amount of research devoted to nanostructured transparent conducting materials (TCM), which play a pivotal role in many modern devices such as solar cells, flexible light-emitting devices, touch screens, electromagnetic devices, and flexible transparent thin film heaters. Currently, the most commonly used TCM for such applications (ITO: Indium Tin oxide) suffers from two major drawbacks: brittleness and indium scarcity. Among emerging transparent electrodes, silver nanowire (AgNW) networks appear to be a promising substitute to ITO since such electrically percolating networks exhibit excellent properties with sheet resistance lower than 10 Ω/sq and optical transparency of 90%, fulfilling the requirements of most applications. In addition, AgNW networks also exhibit very good mechanical flexibility. The fabrication of these electrodes involves low-temperature processing steps and scalable methods, thus making them appropriate for future use as low-cost transparent electrodes in flexible electronic devices. This contribution aims to briefly present the main properties of AgNW based transparent electrodes as well as some considerations relating to their efficient integration in devices. The influence of network density, nanowire sizes, and post treatments on the properties of AgNW networks will also be evaluated. In addition to a general overview of AgNW networks, we focus on two important aspects: (i) network instabilities as well as an efficient Atomic Layer Deposition (ALD) coating which clearly enhances AgNW network stability and (ii) modelling to better understand the physical properties of these networks. Full article
(This article belongs to the Special Issue Advances in Transparent Conducting Materials)
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Open AccessArticle The Investigation of High Quality PEDOT:PSS Film by Multilayer-Processing and Acid Treatment
Energies 2017, 10(5), 716; doi:10.3390/en10050716
Received: 29 March 2017 / Revised: 27 April 2017 / Accepted: 15 May 2017 / Published: 18 May 2017
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Abstract
In this study, we have investigated the performance of multilayer films of poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) treated with one of the perfluorinated carboxylic acids, named trifluoroacetic acid (TFA). According to the increased density of the PEDOT chain under unit area conditions, the sheet resistance (R
[...] Read more.
In this study, we have investigated the performance of multilayer films of poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) treated with one of the perfluorinated carboxylic acids, named trifluoroacetic acid (TFA). According to the increased density of the PEDOT chain under unit area conditions, the sheet resistance (Rsq) has improved from 300 to 65 Ω/sq through additional processing of PEDOT:PSS from single layer to multilayer. After the further treatment with TFA, however, the Rsq of the multilayer PEDOT:PSS was enhanced to 45 Ω/sq, leading to the decline of film thickness from 400 to 270 nm. Both conductivity and work function based on X-ray photoelectron spectroscopy results have built a breakthrough by double-processing because of the higher density of conductive PEDOT chains and the increase of 0.4 eV alternatives to typical indium tin oxide substrate, respectively. This improvement is contributed to the development of more effective transparent electrodes. Full article
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Open AccessArticle ITO-Free Transparent Organic Solar Cell with Distributed Bragg Reflector for Solar Harvesting Windows
Energies 2017, 10(5), 707; doi:10.3390/en10050707
Received: 30 March 2017 / Revised: 8 May 2017 / Accepted: 11 May 2017 / Published: 17 May 2017
Cited by 1 | Viewed by 444 | PDF Full-text (5288 KB) | HTML Full-text | XML Full-text
Abstract
We demonstrated an indium tin oxide (ITO)-free, highly transparent organic solar cell with the potential to be integrated into window panes for energy harvesting purposes. A transparent, conductive ZnO/Ag/ZnO multilayer electrode and a Ag:Ca thin film electrode were used in this transparent device
[...] Read more.
We demonstrated an indium tin oxide (ITO)-free, highly transparent organic solar cell with the potential to be integrated into window panes for energy harvesting purposes. A transparent, conductive ZnO/Ag/ZnO multilayer electrode and a Ag:Ca thin film electrode were used in this transparent device as the bottom and top electrode, respectively. To further improve the transmittance of the solar cell, the thickness of the top ZnO layer was investigated both experimentally and with simulations. An average visible transmittance of >60% was reached, with a maximum transmittance of 73% at 556 nm. Both top and bottom illumination of the solar cell generated comparable power conversion efficiencies, which indicates the wide application of this solar cell structure. In addition, we fabricated distributed Bragg reflector mirrors with sputtered SiO2 and TiO2, which efficiently increased the power conversion efficiency over 20% for the solar cells on glass and poly(ethylene terephthalate) (PET) substrates. Full article
(This article belongs to the Special Issue Solar Energy Application in Buildings)
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Open AccessArticle Transparent Conducting Film Fabricated by Metal Mesh Method with Ag and Cu@Ag Mixture Nanoparticle Pastes
Metals 2017, 7(5), 176; doi:10.3390/met7050176
Received: 7 March 2017 / Revised: 18 April 2017 / Accepted: 11 May 2017 / Published: 16 May 2017
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Abstract
Transparent conducting electrode film is highly desirable for application in touch screen panels (TSPs), flexible and wearable displays, sensors, and actuators. A sputtered film of indium tin oxide (ITO) shows high transmittance (90%) at low sheet resistance (50 Ω/cm2). However, ITO
[...] Read more.
Transparent conducting electrode film is highly desirable for application in touch screen panels (TSPs), flexible and wearable displays, sensors, and actuators. A sputtered film of indium tin oxide (ITO) shows high transmittance (90%) at low sheet resistance (50 Ω/cm2). However, ITO films lack mechanical flexibility, especially under bending stress, and have limitation in application to large-area TSPs (over 15 inches) due to the trade-off in high transmittance and low sheet resistance properties. One promising solution is to use metal mesh-type transparent conducting film, especially for touch panel application. In this work, we investigated such inter-related issues as UV imprinting process to make a trench layer pattern, the synthesis of core-shell-type Ag and Cu@Ag composite nanoparticles and their paste formulation, the filling of Ag and Cu@Ag mixture nanoparticle paste to the trench layer, and touch panel fabrication processes. Full article
(This article belongs to the Special Issue Metal Matrix Composites)
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Open AccessArticle Electrochemical Detection of Dopamine Using 3D Porous Graphene Oxide/Gold Nanoparticle Composites
Sensors 2017, 17(4), 861; doi:10.3390/s17040861
Received: 2 March 2017 / Revised: 6 April 2017 / Accepted: 11 April 2017 / Published: 14 April 2017
Cited by 1 | Viewed by 552 | PDF Full-text (2380 KB) | HTML Full-text | XML Full-text | Supplementary Files
Abstract
The detection of dopamine in a highly sensitive and selective manner is crucial for the early diagnosis of a number of neurological diseases/disorders. Here, a report on a new platform for the electrochemical detection of dopamine with a considerable accuracy that comprises a
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The detection of dopamine in a highly sensitive and selective manner is crucial for the early diagnosis of a number of neurological diseases/disorders. Here, a report on a new platform for the electrochemical detection of dopamine with a considerable accuracy that comprises a 3D porous graphene oxide (pGO)/gold nanoparticle (GNP)/pGO composite-modified indium tin oxide (ITO) is presented. The pGO was first synthesized and purified by ultrasonication and centrifugation, and it was then further functionalized on the surface of a GNP-immobilized ITO electrode. Remarkably, owing to the synergistic effects of the pGO and GNPs, the 3D pGO-GNP-pGO-modified ITO electrode showed a superior dopamine-detection performance compared with the other pGO- or GNP-modified ITO electrodes. The linear range of the newly developed sensing platform is from 0.1 μM to 30 μM with a limit of detection (LOD) of 1.28 μM, which is more precise than the other previously reported GO-functionalized electrodes. Moreover, the 3D pGO-GNP-pGO-modified ITO electrodes maintained their detection capability even in the presence of several interfering molecules (e.g., ascorbic acid, glucose). The proposed platform of the 3D pGO-GNP-pGO-modified ITO electrode could therefore serve as a competent candidate for the development of a dopamine-sensing platform that is potentially applicable for the early diagnosis of various neurological diseases/disorders. Full article
(This article belongs to the Special Issue Micro and Nanofabrication Technologies for Biosensors)
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Open AccessArticle A Urea Potentiometric Biosensor Based on a Thiophene Copolymer
Biosensors 2017, 7(1), 13; doi:10.3390/bios7010013
Received: 11 January 2017 / Revised: 23 February 2017 / Accepted: 27 February 2017 / Published: 3 March 2017
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Abstract
A potentiometric enzyme biosensor is a convenient detector for quantification of urea concentrations in industrial processes, or for monitoring patients with diabetes, kidney damage or liver malfunction. In this work, poly(3-hexylthiophene-co-3-thiopheneacetic acid) (P(3HT-co-3TAA)) was chemically synthesized, characterized and spin-coated
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A potentiometric enzyme biosensor is a convenient detector for quantification of urea concentrations in industrial processes, or for monitoring patients with diabetes, kidney damage or liver malfunction. In this work, poly(3-hexylthiophene-co-3-thiopheneacetic acid) (P(3HT-co-3TAA)) was chemically synthesized, characterized and spin-coated onto conductive indium tin oxide (ITO) glass electrodes. Urease (Urs) was covalently attached to the smooth surface of this copolymer via carbodiimide coupling. The electrochemical behavior and stability of the modified Urs/P(3HT-co-3TAA)/ITO glass electrode were investigated by cyclic voltammetry, and the bound enzyme activity was confirmed by spectrophotometry. Potentiometric response studies indicated that this electrode could determine the concentration of urea in aqueous solutions, with a quasi-Nernstian response up to about 5 mM. No attempt was made to optimize the response speed; full equilibration occurred after 10 min, but the half-time for response was typically <1 min. Full article
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Open AccessArticle Mechanical Properties of ZTO, ITO, and a-Si:H Multilayer Films for Flexible Thin Film Solar Cells
Materials 2017, 10(3), 245; doi:10.3390/ma10030245
Received: 10 January 2017 / Revised: 8 February 2017 / Accepted: 24 February 2017 / Published: 1 March 2017
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Abstract
The behavior of bi- and trilayer coating systems for flexible a-Si:H based solar cells consisting of a barrier, an electrode, and an absorption layer is studied under mechanical load. First, the film morphology, stress, Young’s modulus, and crack onset strain (COS) were analyzed
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The behavior of bi- and trilayer coating systems for flexible a-Si:H based solar cells consisting of a barrier, an electrode, and an absorption layer is studied under mechanical load. First, the film morphology, stress, Young’s modulus, and crack onset strain (COS) were analyzed for single film coatings of various thickness on polyethylene terephthalate (PET) substrates. In order to demonstrate the role of the microstructure of a single film on the mechanical behavior of the whole multilayer coating, two sets of InSnOx (indium tin oxide, ITO) conductive coatings were prepared. Whereas a characteristic grain–subgrain structure was observed in ITO-1 films, grain growth was suppressed in ITO-2 films. ITO-1 bilayer coatings showed two-step failure under tensile load with cracks propagating along the ITO-1/a-Si:H-interface, whereas channeling cracks in comparable bi- and trilayers based on amorphous ITO-2 run through all constituent layers. A two-step failure is preferable from an application point of view, as it may lead to only a degradation of the performance instead of the ultimate failure of the device. Hence, the results demonstrate the importance of a fine-tuning of film microstructure not only for excellent electrical properties, but also for a high mechanical performance of flexible devices (e.g., a-Si:H based solar cells) during fabrication in a roll-to-roll process or under service. Full article
(This article belongs to the Special Issue Stretchable and Flexible Electronic Materials & Devices)
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Open AccessArticle A Simple Interfacial Platform for Homogeneous Electrochemical Immunoassays Using a Poly(Vinylimidazole)-Modified Electrode
Sensors 2017, 17(1), 54; doi:10.3390/s17010054
Received: 4 November 2016 / Revised: 22 December 2016 / Accepted: 22 December 2016 / Published: 29 December 2016
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Abstract
In this study, a homogeneous method featuring simple, one-step detection was developed to analyze hippuric acid (HA), a major metabolite of toluene. High sensitivity was achieved with the facile immobilization of poly(vinylimidazole) (PVI) on an indium tin oxide (ITO) electrode. Using a previously
[...] Read more.
In this study, a homogeneous method featuring simple, one-step detection was developed to analyze hippuric acid (HA), a major metabolite of toluene. High sensitivity was achieved with the facile immobilization of poly(vinylimidazole) (PVI) on an indium tin oxide (ITO) electrode. Using a previously developed approach, pentacyanoferrate was coordinated with pyridyl-N ligands, and the redox-active Fe(II/III) centers were bound to Ni(II) ions on the electrode via electrostatic cyanide bridges. The detection was accomplished by the competitive binding of free HA and pentacyanoferrate-(4-aminomethylpyridine-hippuric acid) (Fe-HA, the electron transfer mediator) to the HA antibody on the Ni(II) ions-modified PVI-ITO (Ni-PVI-ITO) electrode. The electrical and physicochemical characterization of the electrode was carried out by cyclic voltammetry, differential pulse voltammetry, field emission scanning electron microscopy, and X-ray photoelectron spectroscopy. At low mediator concentrations, the electrical signals were proportional to the HA concentration between 0.1 µg/mL and 1.0 mg/mL. The same method may be extended to other small organic molecules. Full article
(This article belongs to the Special Issue Electrochemical Immunosensors)
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Open AccessArticle Electrical Impedance Monitoring of C2C12 Myoblast Differentiation on an Indium Tin Oxide Electrode
Sensors 2016, 16(12), 2068; doi:10.3390/s16122068
Received: 31 October 2016 / Revised: 29 November 2016 / Accepted: 30 November 2016 / Published: 5 December 2016
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Abstract
Electrical cell-substrate impedance sensing is increasingly being used for label-free and real-time monitoring of changes in cell morphology and number during cell growth, drug screening, and differentiation. In this study, we evaluated the feasibility of using ECIS to monitor C2C12 myoblast differentiation using
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Electrical cell-substrate impedance sensing is increasingly being used for label-free and real-time monitoring of changes in cell morphology and number during cell growth, drug screening, and differentiation. In this study, we evaluated the feasibility of using ECIS to monitor C2C12 myoblast differentiation using a fabricated indium tin oxide (ITO) electrode-based chip. C2C12 myoblast differentiation on the ITO electrode was validated based on decreases in the mRNA level of MyoD and increases in the mRNA levels of myogenin and myosin heavy chain (MHC). Additionally, MHC expression and morphological changes in myoblasts differentiated on the ITO electrode were comparable to those in cells in the control culture dish. From the monitoring the integration of the resistance change at 21.5 kHz, the cell differentiation was label-free and real-time detectable in 30 h of differentiation (p < 0.05). Full article
(This article belongs to the Special Issue Whole Cell-Based Biosensors and Application)
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Open AccessArticle Enhanced Optoelectronic Properties of PFO/Fluorol 7GA Hybrid Light Emitting Diodes via Additions of TiO2 Nanoparticles
Polymers 2016, 8(9), 334; doi:10.3390/polym8090334
Received: 2 August 2016 / Revised: 21 August 2016 / Accepted: 31 August 2016 / Published: 6 September 2016
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Abstract
The effect of TiO2 nanoparticle (NP) content on the improvement of poly(9,9′-di-n-octylfluorenyl-2,7-diyl) (PFO)/Fluorol 7GA organic light emitting diode (OLED) performance is demonstrated here. The PFO/Fluorol 7GA blend with specific ratios of TiO2 NPs was prepared via a solution blending
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The effect of TiO2 nanoparticle (NP) content on the improvement of poly(9,9′-di-n-octylfluorenyl-2,7-diyl) (PFO)/Fluorol 7GA organic light emitting diode (OLED) performance is demonstrated here. The PFO/Fluorol 7GA blend with specific ratios of TiO2 NPs was prepared via a solution blending method before being spin-coated onto an indium tin oxide (ITO) substrate to act as an emissive layer in OLEDs. A thin aluminum layer as top electrode was deposited onto the emissive layer using the electron beam chamber. Improvement electron injection from the cathode was achieved upon incorporation of TiO2 NPs into the PFO/Fluorol 7GA blend, thus producing devices with intense luminance and lower turn-on voltage. The ITO/(PFO/Fluorol 7GA/TiO2)/Al OLED device exhibited maximum electroluminescence intensity and luminance at 25 wt % of TiO2 NPs, while maximum luminance efficiency was achieved with 15 wt % TiO2 NP content. In addition, this work proved that the performance of the devices was strongly affected by the surface morphology, which in turn depended on the TiO2 NP content. Full article
(This article belongs to the Special Issue Nanocomposites of Polymers and Inorganic Particles 2016)
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Open AccessFeature PaperArticle Optical and Electrical Performance of MOS-Structure Silicon Solar Cells with Antireflective Transparent ITO and Plasmonic Indium Nanoparticles under Applied Bias Voltage
Materials 2016, 9(8), 682; doi:10.3390/ma9080682
Received: 31 May 2016 / Revised: 27 July 2016 / Accepted: 5 August 2016 / Published: 10 August 2016
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Abstract
This paper reports impressive improvements in the optical and electrical performance of metal-oxide-semiconductor (MOS)-structure silicon solar cells through the incorporation of plasmonic indium nanoparticles (In-NPs) and an indium-tin-oxide (ITO) electrode with periodic holes (perforations) under applied bias voltage. Samples were prepared using a
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This paper reports impressive improvements in the optical and electrical performance of metal-oxide-semiconductor (MOS)-structure silicon solar cells through the incorporation of plasmonic indium nanoparticles (In-NPs) and an indium-tin-oxide (ITO) electrode with periodic holes (perforations) under applied bias voltage. Samples were prepared using a plain ITO electrode or perforated ITO electrode with and without In-NPs. The samples were characterized according to optical reflectance, dark current voltage, induced capacitance voltage, external quantum efficiency, and photovoltaic current voltage. Our results indicate that induced capacitance voltage and photovoltaic current voltage both depend on bias voltage, regardless of the type of ITO electrode. Under a bias voltage of 4.0 V, MOS cells with perforated ITO and plain ITO, respectively, presented conversion efficiencies of 17.53% and 15.80%. Under a bias voltage of 4.0 V, the inclusion of In-NPs increased the efficiency of cells with perforated ITO and plain ITO to 17.80% and 16.87%, respectively. Full article
(This article belongs to the Special Issue Selected Papers from ICASI 2016)
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Open AccessArticle Electrochemical Detection of Hydrazine Using Poly(dopamine)-Modified Electrodes
Sensors 2016, 16(5), 647; doi:10.3390/s16050647
Received: 5 March 2016 / Revised: 22 April 2016 / Accepted: 3 May 2016 / Published: 5 May 2016
Cited by 3 | Viewed by 839 | PDF Full-text (2478 KB) | HTML Full-text | XML Full-text | Supplementary Files
Abstract
We have developed a simple and selective method for the electrochemical detection of hydrazine (HZ) using poly(dopamine) (pDA)-modified indium tin oxide (ITO) electrodes. Modification with pDA was easily achieved by submerging the ITO electrode in a DA solution for 30 min. The electrocatalytic
[...] Read more.
We have developed a simple and selective method for the electrochemical detection of hydrazine (HZ) using poly(dopamine) (pDA)-modified indium tin oxide (ITO) electrodes. Modification with pDA was easily achieved by submerging the ITO electrode in a DA solution for 30 min. The electrocatalytic oxidation of HZ on the pDA-modified ITO electrode was measured by cyclic voltammetry. In buffer solution, the concentration range for linear HZ detection was 100 µM–10 mM, and the detection limit was 1 µM. The proposed method was finally used to determine HZ in tap water to simulate the analysis of real samples. This method showed good recovery (94%–115%) and was not affected by the other species present in the tap water samples. Full article
(This article belongs to the Section Chemical Sensors)
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Open AccessArticle Investigations on the Cosputtered ITO-ZnO Transparent Electrode Ohmic Contacts to n-GaN
Appl. Sci. 2016, 6(2), 60; doi:10.3390/app6020060
Received: 29 December 2015 / Revised: 13 February 2016 / Accepted: 16 February 2016 / Published: 22 February 2016
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Abstract
Transparent indium tin oxide (ITO) and cosputtered ITO-zinc oxide (ZnO) films’ contacts to an n-GaN epilayer were investigated. Both of these electrodes’ contact to the n-GaN epilayer showed Schottky behavior, although the contact resistance of the ITO-ZnO/n-GaN system was
[...] Read more.
Transparent indium tin oxide (ITO) and cosputtered ITO-zinc oxide (ZnO) films’ contacts to an n-GaN epilayer were investigated. Both of these electrodes’ contact to the n-GaN epilayer showed Schottky behavior, although the contact resistance of the ITO-ZnO/n-GaN system was lower than that of the ITO/n-GaN system. By placing a thin Ti interlayer between the ITO-ZnO/n-GaN interface, nonalloyed ohmic contact was achieved. The inset Ti interlayer was both beneficial both for enhancing the outdiffusion of the nitrogen atoms at the surface of the n-GaN and suppressing the indiffusion of oxygen atoms from the surface of the ITO-ZnO to n-GaN. The figure-of-merit (FOM), evaluated from the specific contact resistance and optical property of the Ti/ITO-ZnO system’s contact to the n-GaN epilayer, was optimized further at an adequate thickness of the Ti interlayer. Full article
(This article belongs to the Special Issue Selected Papers from the 2015 International Conference on Inventions)
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Open AccessArticle A Novel Photoelectrochemical Biosensor for Tyrosinase and Thrombin Detection
Sensors 2016, 16(1), 135; doi:10.3390/s16010135
Received: 16 December 2015 / Revised: 14 January 2016 / Accepted: 16 January 2016 / Published: 21 January 2016
Cited by 6 | Viewed by 1047 | PDF Full-text (903 KB) | HTML Full-text | XML Full-text
Abstract
A novel photoelectrochemical biosensor for step-by-step assay of tyrosinase and thrombin was fabricated based on the specific interactions between the designed peptide and the target enzymes. A peptide chain with a special sequence which contains a positively charged lysine-labeled terminal, tyrosine at the
[...] Read more.
A novel photoelectrochemical biosensor for step-by-step assay of tyrosinase and thrombin was fabricated based on the specific interactions between the designed peptide and the target enzymes. A peptide chain with a special sequence which contains a positively charged lysine-labeled terminal, tyrosine at the other end and a cleavage site recognized by thrombin between them was designed. The designed peptide can be fixed on surface of the CdTe quantum dots (QDs)-modified indium-tin oxide (ITO) electrode through electrostatic attraction to construct the photoelectrochemical biosensor. The tyrosinase target can catalyze the oxidization of tyrosine by oxygen into ortho-benzoquinone residues, which results in a decrease in the sensor photocurrent. Subsequently, the cleavage site could be recognized and cut off by another thrombin target, restoring the sensor photocurrent. The decrease or increase of photocurrent in the sensor enables us to assay tyrosinase and thrombin. Thus, the detection of tyrosinase and thrombin can be achieved in the linear range from 2.6 to 32 μg/mL and from 4.5 to 100 μg/mL with detection limits of 1.5 μg/mL and 1.9 μg/mL, respectively. Most importantly, this strategy shall allow us to detect different classes of enzymes simultaneously by designing various enzyme-specific peptide substrates. Full article
(This article belongs to the Special Issue Microbial and Enzymatic Biosensors)
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Open AccessArticle Influence of Oxygen Concentration on the Performance of Ultra-Thin RF Magnetron Sputter Deposited Indium Tin Oxide Films as a Top Electrode for Photovoltaic Devices
Materials 2016, 9(1), 63; doi:10.3390/ma9010063
Received: 17 December 2015 / Revised: 6 January 2016 / Accepted: 14 January 2016 / Published: 20 January 2016
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Abstract
The opportunity for substantial efficiency enhancements of thin film hydrogenated amorphous silicon (a-Si:H) solar photovoltaic (PV) cells using plasmonic absorbers requires ultra-thin transparent conducting oxide top electrodes with low resistivity and high transmittances in the visible range of the electromagnetic spectrum. Fabricating ultra-thin
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The opportunity for substantial efficiency enhancements of thin film hydrogenated amorphous silicon (a-Si:H) solar photovoltaic (PV) cells using plasmonic absorbers requires ultra-thin transparent conducting oxide top electrodes with low resistivity and high transmittances in the visible range of the electromagnetic spectrum. Fabricating ultra-thin indium tin oxide (ITO) films (sub-50 nm) using conventional methods has presented a number of challenges; however, a novel method involving chemical shaving of thicker (greater than 80 nm) RF sputter deposited high-quality ITO films has been demonstrated. This study investigates the effect of oxygen concentration on the etch rates of RF sputter deposited ITO films to provide a detailed understanding of the interaction of all critical experimental parameters to help create even thinner layers to allow for more finely tune plasmonic resonances. ITO films were deposited on silicon substrates with a 98-nm, thermally grown oxide using RF magnetron sputtering with oxygen concentrations of 0, 0.4 and 1.0 sccm and annealed at 300 °C air ambient. Then the films were etched using a combination of water and hydrochloric and nitric acids for 1, 3, 5 and 8 min at room temperature. In-between each etching process cycle, the films were characterized by X-ray diffraction, atomic force microscopy, Raman Spectroscopy, 4-point probe (electrical conductivity), and variable angle spectroscopic ellipsometry. All the films were polycrystalline in nature and highly oriented along the (222) reflection. Ultra-thin ITO films with record low resistivity values (as low as 5.83 × 10−4 Ω·cm) were obtained and high optical transparency is exhibited in the 300–1000 nm wavelength region for all the ITO films. The etch rate, preferred crystal lattice growth plane, d-spacing and lattice distortion were also observed to be highly dependent on the nature of growth environment for RF sputter deposited ITO films. The structural, electrical, and optical properties of the ITO films are discussed with respect to the oxygen ambient nature and etching time in detail to provide guidance for plasmonic enhanced a-Si:H solar PV cell fabrication. Full article
(This article belongs to the Special Issue Photovoltaic Materials and Electronic Devices) Printed Edition available
Open AccessArticle Formation of High-Purity Indium Oxide Nanoparticles and Their Application to Sensitive Detection of Ammonia
Sensors 2015, 15(12), 31930-31938; doi:10.3390/s151229895
Received: 22 October 2015 / Revised: 7 December 2015 / Accepted: 11 December 2015 / Published: 17 December 2015
Cited by 2 | Viewed by 954 | PDF Full-text (3984 KB) | HTML Full-text | XML Full-text
Abstract
High-purity In2O3 nanoparticles were recovered from scrap indium tin oxide substrates in a stepwise process involving acidic leaching, liquid-liquid extraction with a phosphine oxide extractant, and combustion of the organic phase. The morphological and structural parameters of the recovered nanoparticles
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High-purity In2O3 nanoparticles were recovered from scrap indium tin oxide substrates in a stepwise process involving acidic leaching, liquid-liquid extraction with a phosphine oxide extractant, and combustion of the organic phase. The morphological and structural parameters of the recovered nanoparticles were investigated to support the formation of the desired products. These In2O3 nanoparticles were used for sensitive sensing of ammonia gas using a four-probe electrode device. The proposed sensor offered very quick response time (around 10 s) and highly sensitive detection of ammonia (at a detection limit of 1 ppm). Full article
(This article belongs to the Special Issue The Use of New and/or Improved Materials for Sensing Applications)
Open AccessArticle Effects of Electrodes on the Switching Behavior of Strontium Titanate Nickelate Resistive Random Access Memory
Materials 2015, 8(10), 7191-7198; doi:10.3390/ma8105374
Received: 30 August 2015 / Revised: 11 October 2015 / Accepted: 19 October 2015 / Published: 26 October 2015
Cited by 10 | Viewed by 1031 | PDF Full-text (3811 KB) | HTML Full-text | XML Full-text
Abstract
Strontium titanate nickelate (STN) thin films on indium tin oxide (ITO)/glass substrate were synthesized using the sol-gel method for resistive random access memory (RRAM) applications. Aluminum (Al), titanium (Ti), tungsten (W), gold (Au) and platinum (Pt) were used as top electrodes in the
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Strontium titanate nickelate (STN) thin films on indium tin oxide (ITO)/glass substrate were synthesized using the sol-gel method for resistive random access memory (RRAM) applications. Aluminum (Al), titanium (Ti), tungsten (W), gold (Au) and platinum (Pt) were used as top electrodes in the STN-based RRAM to probe the switching behavior. The bipolar resistive switching behavior of the set and reset voltages is in opposite bias in the Al/STN/ITO and Pt/STN/ITO RRAMs, which can be partly ascribed to the different work functions of top electrodes in the ITO. Analyses of the fitting results and temperature-dependent performances showed that the Al/STN/ITO switching was mainly attributed to the absorption/release of oxygen-based functional groups, whereas the Pt/STN/ITO switching can be associated with the diffusion of metal electrode ions. The Al/STN/ITO RRAM demonstrated a high resistance ratio of >106 between the high-resistance state (HRS) and the low-resistance state (LRS), as well as a retention ability of >105 s. Furthermore, the Pt/STN/ITO RRAM displayed a HRS/LRS resistance ratio of >103 and a retention ability of >105 s. Full article
(This article belongs to the Special Issue Selected Papers from ICASI 2015)
Open AccessArticle An Electrochemical Glucose Sensor Based on Zinc Oxide Nanorods
Sensors 2015, 15(8), 18714-18723; doi:10.3390/s150818714
Received: 13 May 2015 / Revised: 29 June 2015 / Accepted: 22 July 2015 / Published: 30 July 2015
Cited by 14 | Viewed by 1957 | PDF Full-text (1445 KB) | HTML Full-text | XML Full-text
Abstract
A glucose electrochemical sensor based on zinc oxide (ZnO) nanorods was investigated. The hydrothermal sol–gel growth method was utilized to grow ZnO nanorods on indium tin oxide-coated glass substrates. The total active area of the working electrode was 0.3 × 0.3 cm2
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A glucose electrochemical sensor based on zinc oxide (ZnO) nanorods was investigated. The hydrothermal sol–gel growth method was utilized to grow ZnO nanorods on indium tin oxide-coated glass substrates. The total active area of the working electrode was 0.3 × 0.3 cm2 where titanium metal was deposited to enhance the contact. Well aligned hexagonal structured ZnO nanorods with a diameter from 68 to 116 nm were obtained. The excitonic peak obtained from the absorbance spectroscopy was observed at ~370 nm. The dominant peak of Raman spectroscopy measurement was at 440 cm−1, matching with the lattice vibration of ZnO. The uniform distribution of the GOx and Nafion membrane that has been done using spin coating technique at 4000 rotations per minute helps in enhancing the ion exchange and increasing the sensitivity of the fabricated electrochemical sensor. The amperometric response of the fabricated electrochemical sensor was 3 s. The obtained sensitivity of the fabricated ZnO electrochemical sensor was 10.911 mA/mM·cm2 and the lower limit of detection was 0.22 µM. Full article
Open AccessReview Functionalized Solid Electrodes for Electrochemical Biosensing of Purine Nucleobases and Their Analogues: A Review
Sensors 2015, 15(1), 1564-1600; doi:10.3390/s150101564
Received: 27 November 2014 / Accepted: 4 January 2015 / Published: 14 January 2015
Cited by 14 | Viewed by 1493 | PDF Full-text (1997 KB) | HTML Full-text | XML Full-text
Abstract
Interest in electrochemical analysis of purine nucleobases and few other important purine derivatives has been growing rapidly. Over the period of the past decade, the design of electrochemical biosensors has been focused on achieving high sensitivity and efficiency. The range of existing electrochemical
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Interest in electrochemical analysis of purine nucleobases and few other important purine derivatives has been growing rapidly. Over the period of the past decade, the design of electrochemical biosensors has been focused on achieving high sensitivity and efficiency. The range of existing electrochemical methods with carbon electrode displays the highest rate in the development of biosensors. Moreover, modification of electrode surfaces based on nanomaterials is frequently used due to their extraordinary conductivity and surface to volume ratio. Different strategies for modifying electrode surfaces facilitate electron transport between the electrode surface and biomolecules, including DNA, oligonucleotides and their components. This review aims to summarize recent developments in the electrochemical analysis of purine derivatives, as well as discuss different applications. Full article
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Open AccessArticle Development of a Photosynthetic Microbial Electrochemical Cell (PMEC) Reactor Coupled with Dark Fermentation of Organic Wastes: Medium Term Perspectives
Energies 2015, 8(1), 399-429; doi:10.3390/en8010399
Received: 29 August 2014 / Accepted: 16 December 2014 / Published: 13 January 2015
Cited by 2 | Viewed by 1840 | PDF Full-text (1311 KB) | HTML Full-text | XML Full-text
Abstract
In this article the concept, the materials and the exploitation potential of a photosynthetic microbial electrochemical cell for the production of hydrogen driven by solar power are investigated. In a photosynthetic microbial electrochemical cell, which is based on photosynthetic microorganisms confined to an
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In this article the concept, the materials and the exploitation potential of a photosynthetic microbial electrochemical cell for the production of hydrogen driven by solar power are investigated. In a photosynthetic microbial electrochemical cell, which is based on photosynthetic microorganisms confined to an anode and heterotrophic bacteria confined to a cathode, water is split by bacteria hosted in the anode bioactive film. The generated electrons are conveyed through external “bio-appendages” developed by the bacteria to transparent nano-pillars made of indium tin oxide (ITO), Fluorine-doped tin oxide (FTO) or other conducting materials, and then transferred to the cathode. On the other hand, the generated protons diffuse to the cathode via a polymer electrolyte membrane, where they are reduced by the electrons by heterotrophic bacteria growing attached to a similar pillared structure as that envisaged for the anode and supplemented with a specific low cost substrate (e.g., organic waste, anaerobic digestion outlet). The generated oxygen is released to the atmosphere or stored, while the produced pure hydrogen leaves the electrode through the porous layers. In addition, the integration of the photosynthetic microbial electrochemical cell system with dark fermentation as acidogenic step of anaerobic digester, which is able to produce additional H2, and the use of microbial fuel cell, feed with the residues of dark fermentation (mainly volatile fatty acids), to produce the necessary extra-bias for the photosynthetic microbial electrochemical cell is here analyzed to reveal the potential benefits to this novel integrated technology. Full article
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Open AccessArticle Characterization of Piezoresistive PEDOT:PSS Pressure Sensors with Inter-Digitated and Cross-Point Electrode Structures
Sensors 2015, 15(1), 818-831; doi:10.3390/s150100818
Received: 11 November 2014 / Accepted: 25 December 2014 / Published: 5 January 2015
Cited by 5 | Viewed by 1485 | PDF Full-text (3456 KB) | HTML Full-text | XML Full-text
Abstract
The piezoresistive characteristics of poly(3,4-ethylenedioxythiophene):polystyrene sulfonate (PEDOT:PSS) pressure sensors with inter-digitated (IDE) and cross-point electrode (CPE) structures have been investigated. A small variation of the resistance of the pressure sensors with IDE without bottom indium-tin-oxide (b-ITO) film and with CPE structures was observed
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The piezoresistive characteristics of poly(3,4-ethylenedioxythiophene):polystyrene sulfonate (PEDOT:PSS) pressure sensors with inter-digitated (IDE) and cross-point electrode (CPE) structures have been investigated. A small variation of the resistance of the pressure sensors with IDE without bottom indium-tin-oxide (b-ITO) film and with CPE structures was observed owing to the single carrier-conducting pathway. For the IDE pressure sensors with b-ITO, the piezoresistive characteristics at low and high pressure were similar to those of the pressure sensors with IDE without b-ITO and with CPE structures, respectively, leading to increased piezoresistive pressure sensitivity as the PEDOT:PSS film thickness decreased. A maximum sensitivity of more than 42 kΩ/Pa was achieved. When the normal pressure was applied, the increased number of conducting points or the reduced distance between the PEDOT oligomers within the PEDOT:PSS film resulted in a decrease of the resistance. The piezoresistive pressure sensors with a single carrier-conducting pathway, i.e., IDE without b-ITO and CPE structures, exhibited a small relaxation time and a superior reversible operation, which can be advantageous for fast piezoresistive response applications. Full article
(This article belongs to the Section Physical Sensors)
Open AccessReview Emerging Transparent Conducting Electrodes for Organic Light Emitting Diodes
Electronics 2014, 3(1), 190-204; doi:10.3390/electronics3010190
Received: 21 January 2014 / Revised: 1 March 2014 / Accepted: 12 March 2014 / Published: 21 March 2014
Cited by 16 | Viewed by 2693 | PDF Full-text (2674 KB) | HTML Full-text | XML Full-text
Abstract
Organic light emitting diodes (OLEDs) have attracted much attention in recent years as next generation lighting and displays, due to their many advantages, including superb performance, mechanical flexibility, ease of fabrication, chemical versatility, etc. In order to fully realize the highly flexible
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Organic light emitting diodes (OLEDs) have attracted much attention in recent years as next generation lighting and displays, due to their many advantages, including superb performance, mechanical flexibility, ease of fabrication, chemical versatility, etc. In order to fully realize the highly flexible features, reduce the cost and further improve the performance of OLED devices, replacing the conventional indium tin oxide with better alternative transparent conducting electrodes (TCEs) is a crucial step. In this review, we focus on the emerging alternative TCE materials for OLED applications, including carbon nanotubes (CNTs), metallic nanowires, conductive polymers and graphene. These materials are selected, because they have been applied as transparent electrodes for OLED devices and achieved reasonably good performance or even higher device performance than that of indium tin oxide (ITO) glass. Various electrode modification techniques and their effects on the device performance are presented. The effects of new TCEs on light extraction, device performance and reliability are discussed. Highly flexible, stretchable and efficient OLED devices are achieved based on these alternative TCEs. These results are summarized for each material. The advantages and current challenges of these TCE materials are also identified. Full article
(This article belongs to the Special Issue Organic Semiconductors) Printed Edition available
Open AccessArticle Evaluation of Biofuel Cells with Hemoglobin as Cathodic Electrocatalysts for Hydrogen Peroxide Reduction on Bare Indium-Tin-Oxide Electrodes
Energies 2014, 7(1), 1-12; doi:10.3390/en7010001
Received: 1 November 2013 / Revised: 9 December 2013 / Accepted: 13 December 2013 / Published: 20 December 2013
Cited by 3 | Viewed by 2205 | PDF Full-text (967 KB) | HTML Full-text | XML Full-text
Abstract
A biofuel cell (BFC) cathode has been developed based on direct electron transfer (DET) of hemoglobin (Hb) molecules with an indium-tin-oxide (ITO) electrode and their electrocatalysis for reduction of hydrogen peroxide (H2O2). In this study, the ITO-coated glass plates
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A biofuel cell (BFC) cathode has been developed based on direct electron transfer (DET) of hemoglobin (Hb) molecules with an indium-tin-oxide (ITO) electrode and their electrocatalysis for reduction of hydrogen peroxide (H2O2). In this study, the ITO-coated glass plates or porous glasses were prepared by using a chemical vapor deposition (CVD) method and examined the electrochemical characteristics of the formed ITO in pH 7.4 of phosphate buffered saline (PBS) solutions containing and not containing Hb. In half-cell measurements, the reduction current of H2O2 due to the electrocatalytic activity of Hb increased with decreasing electrode potential from around 0.1 V versus Ag|AgCl|KCl(satd.) in the PBS solution. The practical open-circuit voltage (OCV) on BFCs utilizing H2O2 reduction at the Hb-ITO cathode with a hydrogen (H2) oxidation anode at a platinum (Pt) electrode was expected to be at least 0.74 V from the theoretical H2 oxidation potential of −0.64 V versus Ag|AgCl|KCl(satd.) in pH 7.4. The assembled single cell using the ITO-coated glass plate showed the OCV of 0.72 V and the maximum power density of 3.1 µW cm−2. The maximum power per single cell was recorded at 21.5 µW by using the ITO-coated porous glass. Full article
(This article belongs to the Special Issue Biomass and Biofuels 2013)
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Open AccessArticle Poly(lactic acid)/Carbon Nanotube Fibers as Novel Platforms for Glucose Biosensors
Biosensors 2012, 2(1), 70-82; doi:10.3390/bios2010070
Received: 16 January 2012 / Revised: 11 February 2012 / Accepted: 24 February 2012 / Published: 27 February 2012
Cited by 12 | Viewed by 3179 | PDF Full-text (293 KB) | HTML Full-text | XML Full-text
Abstract
The focus of this paper is the development and investigation of properties of new nanostructured architecture for biosensors applications. Highly porous nanocomposite fibers were developed for use as active materials in biosensors. The nanocomposites comprised poly(lactic acid)(PLA)/multi-walled carbon nanotube (MWCNT) fibers obtained via
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The focus of this paper is the development and investigation of properties of new nanostructured architecture for biosensors applications. Highly porous nanocomposite fibers were developed for use as active materials in biosensors. The nanocomposites comprised poly(lactic acid)(PLA)/multi-walled carbon nanotube (MWCNT) fibers obtained via solution-blow spinning onto indium tin oxide (ITO) electrodes. The electrocatalytic properties of nanocomposite-modified ITO electrodes were investigated toward hydrogen peroxide (H2O2) detection. We investigated the effect of carbon nanotube concentration and the time deposition of fibers on the sensors properties, viz., sensitivity and limit of detection. Cyclic voltammetry experiments revealed that the nanocomposite-modified electrodes displayed enhanced activity in the electrochemical reduction of H2O2, which offers a number of attractive features to be explored in development of an amperometric biosensor. Glucose oxidase (GOD) was further immobilized by drop coating on an optimized ITO electrode covered by poly(lactic acid)/carbon nanotube nanofibrous mats. The optimum biosensor response was linear up to 800 mM of glucose with a sensitivity of 358 nA·mM−1 and a Michaelis-Menten constant (KM) of 4.3 mM. These results demonstrate that the solution blow spun nanocomposite fibers have great potential for application as amperometric biosensors due to their high surface to volume ratio, high porosity and permeability of the substrate. The latter features may significantly enhance the field of glucose biosensors. Full article
(This article belongs to the Special Issue Electrochemical Based Biosensors)
Open AccessTechnical Note Effect of Counter Electrode in Electroformation of Giant Vesicles
Membranes 2011, 1(4), 345-353; doi:10.3390/membranes1040345
Received: 14 September 2011 / Revised: 10 October 2011 / Accepted: 17 November 2011 / Published: 24 November 2011
Cited by 3 | Viewed by 2308 | PDF Full-text (2245 KB) | HTML Full-text | XML Full-text
Abstract
Electroformation of cell-sized lipid membrane vesicles (giant vesicles, GVs), from egg yolk phosphatidylcholine, was examined varying the shape of the counter electrode. Instead of a planar ITO (indium tin oxide) electrode commonly used, platinum wire mesh was employed as a counter electrode facing
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Electroformation of cell-sized lipid membrane vesicles (giant vesicles, GVs), from egg yolk phosphatidylcholine, was examined varying the shape of the counter electrode. Instead of a planar ITO (indium tin oxide) electrode commonly used, platinum wire mesh was employed as a counter electrode facing lipid deposit on a planar formation electrode. The modification did not significantly alter GV formation, and many GVs of 30–50 µm, some as large as 100 µm, formed as with the standard setup, indicating that a counter electrode does not have to be a complete plane. When the counter electrode was reduced to a set of two parallel platinum wires, GV formation deteriorated. Some GVs formed, but only in close proximity to the counter electrode. Lower electric voltage with this setup no longer yielded GVs. Instead, a large onion-like multilamellar structure was observed. The deteriorated GV formation and the formation of a multilamellar structure seemed to indicate the weakened effect of the electric field on lipid deposit due to insufficient coverage with a small counter electrode. Irregular membranous objects formed by spontaneous swelling of lipid without electric voltage gradually turned into multilamellar structure upon following application of voltage. No particular enhancement of GV formation was observed when lipid deposit on a wire formation electrode was used in combination with a large planar counter electrode. Full article
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Open AccessArticle Electroformation of Giant Vesicles on Indium Tin Oxide (ITO)-Coated Poly(ethylene terephthalate) (PET) Electrodes
Membranes 2011, 1(2), 109-118; doi:10.3390/membranes1020109
Received: 12 April 2011 / Revised: 17 May 2011 / Accepted: 19 May 2011 / Published: 26 May 2011
Cited by 4 | Viewed by 2576 | PDF Full-text (672 KB) | HTML Full-text | XML Full-text | Supplementary Files
Abstract
Electroformation of cell-sized lipid membrane vesicles (giant vesicles, GVs) from egg yolk phosphatidylcholine was examined using a poly(ethylene terephthalate) sheet coated with indium tin oxide (ITO-PET) as the electrode material. With sinusoidal ac voltage, GV formation occurred in a similar manner to that
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Electroformation of cell-sized lipid membrane vesicles (giant vesicles, GVs) from egg yolk phosphatidylcholine was examined using a poly(ethylene terephthalate) sheet coated with indium tin oxide (ITO-PET) as the electrode material. With sinusoidal ac voltage, GV formation occurred in a similar manner to that on an ITO-glass electrode widely used in electroformation. Difference in the specific electrical resistance of ITO-PET did not significantly affect electroformation. The present results indicate that ITO-PET may be used as more flexible and less expensive electrode material in electroformation. In order to obtain insights into electroformation, other electric voltage forms, static dc and dc pulses, were also tested in place of commonly used sinusoidal ac. Under the present conditions, the best GV formation was observed with dc pulses of negative polarity. The result with static dc demonstrated that the mechanical vibration of swelling lipid seen with sinusoidal ac voltage was not essential for GV formation. On the positive electrode, the electroswelling of lipid mainly yielded non-spherical membranous objects. Pre-application of positive dc voltage on lipid hindered GV formation in electroswelling of the lipid with ac. Full article
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Open AccessArticle Study of Sodium Ion Selective Electrodes and Differential Structures with Anodized Indium Tin Oxide
Sensors 2010, 10(3), 1798-1809; doi:10.3390/s100301798
Received: 23 December 2009 / Revised: 20 January 2010 / Accepted: 2 February 2010 / Published: 4 March 2010
Cited by 15 | Viewed by 4869 | PDF Full-text (230 KB) | HTML Full-text | XML Full-text
Abstract
The objective of this work is the study and characterization of anodized indium tin oxide (anodized-ITO) as a sodium ion selective electrode and differential structures including a sodium-selective-membrane/anodized-ITO as sensor 1, an anodized-ITO membrane as the contrast sensor 2, and an ITO as
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The objective of this work is the study and characterization of anodized indium tin oxide (anodized-ITO) as a sodium ion selective electrode and differential structures including a sodium-selective-membrane/anodized-ITO as sensor 1, an anodized-ITO membrane as the contrast sensor 2, and an ITO as the reference electrode. Anodized-ITO was fabricated by anodic oxidation at room temperature, a low cost and simple manufacture process that makes it easy to control the variation in film resistance. The anodized-ITO based on EGFET structure has good linear pH sensitivity, approximately 54.44 mV/pH from pH 2 to pH 12. The proposed sodium electrodes prepared by PVC-COOH, DOS embedding colloid, and complex Na-TFBD and ionophore B12C4, show good sensitivity at 52.48 mV/decade for 10−4 M to 1 M, and 29.96 mV/decade for 107 M to 104 M. The sodium sensitivity of the differential sodium-sensing device is 58.65 mV/decade between 10−4 M and 1 M, with a corresponding linearity of 0.998; and 19.17 mV/decade between 105 M and 104 M. Full article
(This article belongs to the Special Issue ISFET Sensors)
Open AccessArticle Fabrication of a Multi-Walled Nanotube (MWNT) Ionic Liquid Electrode and Its Application for Sensing Phenolics in Red Wines
Sensors 2009, 9(9), 6701-6714; doi:10.3390/s90906701
Received: 16 June 2009 / Revised: 14 July 2009 / Accepted: 18 August 2009 / Published: 26 August 2009
Cited by 19 | Viewed by 7887 | PDF Full-text (889 KB) | HTML Full-text | XML Full-text
Abstract
A multi-walled nanotube (MWNT) ionic liquid was prepared by the immobilization of 1-butylimidazole bromide onto an epoxy group on a poly(glycidyl methacrylate)-grafted MWNT, which was synthesized by radiation-induced graft polymerization of glycidyl methacrylate onto MWNT in an aqueous solution. Subsequently, a MWNT ionic
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A multi-walled nanotube (MWNT) ionic liquid was prepared by the immobilization of 1-butylimidazole bromide onto an epoxy group on a poly(glycidyl methacrylate)-grafted MWNT, which was synthesized by radiation-induced graft polymerization of glycidyl methacrylate onto MWNT in an aqueous solution. Subsequently, a MWNT ionic liquid electrode was fabricated by hand-casting MWNT ionic liquid, tyrosinase, and chitosan solution as a binder on indium tin oxide (ITO) glass. The sensing ranges of the MWNT ionic liquid electrode with immobilized tyrosinase was in the range of 0.01-0.08 mM in a phosphate buffer solution. The optimal conditions such as pH, temperature, and effects of different phenolic compounds were determined. The total phenolic compounds of three commercial red wines were also determined on the tyrosinase-immobilized biosensor. Full article
(This article belongs to the Section Chemical Sensors)
Open AccessCommunication Development of Amperometric Hydrogen Peroxide Sensor Based on Horseradish Peroxidase-Immobilized Poly(Thiophene-co-EpoxyThiophene)
Sensors 2008, 8(7), 4110-4118; doi:10.3390/s8074110
Received: 26 March 2008 / Revised: 3 June 2008 / Accepted: 12 June 2008 / Published: 9 July 2008
Cited by 8 | Viewed by 5325 | PDF Full-text (734 KB) | HTML Full-text | XML Full-text
Abstract
A modified electrode for hydrogen peroxide (H2O2) sensing was prepared via thiophene (Th) with epoxy group. Thiophene (EpoxyTh) with epoxy group was synthesized by reaction of 3-bromothiophene and glycidyl methacrylate (GMA) in acetonitrile according to Heck Reaction. The electrocopolymerization
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A modified electrode for hydrogen peroxide (H2O2) sensing was prepared via thiophene (Th) with epoxy group. Thiophene (EpoxyTh) with epoxy group was synthesized by reaction of 3-bromothiophene and glycidyl methacrylate (GMA) in acetonitrile according to Heck Reaction. The electrocopolymerization of Th and EpoxyTh was performed on the surface of indium tin oxide (ITO) electrode by cycling the potential between -1.0 and +2.5 V in mixture of thiophene (Th) and EpoxyTh. Poly(Th-co- EpoxyTh) grown onto the ITO electrode was successfully confirmed by SEM, AFM, and water contact angle analysis, respectively. Finally, the HRP was immobilized on the surface of poly(Th-co-EpoxyTh) electrode by covalent binding. The amperometric response of the HRP-immobilized poly(Th-co-EpoxyTh) electrode for H2O2 was examined by cyclic voltammetry (CV). The HRP-immobilized poly(Th-co-EpoxyTh) electrode showed linearity from 0.1 to 30 mM H2O2, good reproducibility, and long life time. Full article
Open AccessArticle Opto-Electric Cellular Biosensor Using Optically Transparent Indium Tin Oxide (ITO) Electrodes
Sensors 2008, 8(5), 3257-3270; doi:10.3390/s8053257
Received: 26 January 2008 / Accepted: 16 May 2008 / Published: 19 May 2008
Cited by 22 | Viewed by 5843 | PDF Full-text (3935 KB) | HTML Full-text | XML Full-text
Abstract
Indium tin oxide (ITO) biosensors are used to perform simultaneous optical and electrical measurements in order to examine the dynamic cellular attachment, spreading, and proliferation of endothelial cells (ECs) as well as cytotoxic effects when exposed to cytochalasin D. A detailed description of
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Indium tin oxide (ITO) biosensors are used to perform simultaneous optical and electrical measurements in order to examine the dynamic cellular attachment, spreading, and proliferation of endothelial cells (ECs) as well as cytotoxic effects when exposed to cytochalasin D. A detailed description of the fabrication of these sensors is provided and their superior optical characteristics are qualitatively shown using four different microscopic images. Differential interference contrast microscopy (DICM) images were acquired simultaneously with micro-impedance measurements as a function of frequency and time. A digital image processing algorithm quantified the cell-covered electrode area as a function of time. In addition, cytotoxicity effects, produced by the toxic agent cytochalasin D, were examined using micro-impedance measurements, confocal microscopy images of stained actin-filaments, and interference reflection contrast microscopy (IRCM) capable of examining the bottom morphology of a cell. The results of this study show (1) the dynamic optical and electrical cellular characteristics using optically thin ITO biosensors; (2) qualitative agreement between cell-covered electrode area and electrical impedance during cellular attachment; (3) in vitro cytotoxicity detection of ECs due to 3 mM cytochalasin D. The present opto-electric biosensor system is unique in that a simultaneous and integrated cellular analysis is possible for a variety of living cells. Full article
(This article belongs to the Special Issue Optical Biosensors)
Open AccessArticle Development of a Molecularly Imprinted Biomimetic Electrode
Sensors 2007, 7(8), 1630-1642; doi:10.3390/s7081630
Received: 30 April 2007 / Accepted: 23 August 2007 / Published: 27 August 2007
Cited by 11 | Viewed by 4792 | PDF Full-text (439 KB) | HTML Full-text | XML Full-text
Abstract
The technique of molecular imprinting produces artificial receptor sites in apolymer that can be used in a biomimetic sensor. This research extends previous studies ofa molecularly imprinted polymer (MIP) biomimetic sensor for the small drug theophylline.The presence of theophylline in the biomimetic sensor
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The technique of molecular imprinting produces artificial receptor sites in apolymer that can be used in a biomimetic sensor. This research extends previous studies ofa molecularly imprinted polymer (MIP) biomimetic sensor for the small drug theophylline.The presence of theophylline in the biomimetic sensor was monitored by analyzing thepeak currents from cyclic voltammetry experiments. The functional working range of theMIP modified electrode was 2 - 4 mM theophylline. The concentration of theophyllinethat resulted in the best signal was 3 mM. The MIP sensor showed no response to thestructurally related molecule caffeine, and therefore was selective to the target analytetheophylline. This research will provide the foundation for future studies that will result indurable biomimetic sensors that can offer a viable alternative to current sensors. Full article
(This article belongs to the Special Issue Physiological Sensing)
Open AccessArticle A Novel Supramolecular Assembly Film of Porphyrin Bound DNA: Characterization and Catalytic Behaviors Towards Nitric Oxide
Sensors 2005, 5(4), 171-184; doi:10.3390/s5040171
Received: 28 May 2004 / Accepted: 29 September 2004 / Published: 26 April 2005
Cited by 5 | Viewed by 3722 | PDF Full-text (235 KB) | HTML Full-text | XML Full-text
Abstract
A stable Fe(4-TMPyP)-DNA-PADDA (FePyDP) film was characterized onpyrolytic graphite electrode (PGE) or an indium-tin oxide (ITO) electrode through thesupramolecular interaction between water-soluble iron porphyrin (Fe(4-TMPyP)) and DNAtemplate, where PADDA (poly(acrylamide-co-diallyldimethylammonium chloride) isemployed as a co-immobilizing polymer. Cyclic voltammetry of FePyDP film showed a
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A stable Fe(4-TMPyP)-DNA-PADDA (FePyDP) film was characterized onpyrolytic graphite electrode (PGE) or an indium-tin oxide (ITO) electrode through thesupramolecular interaction between water-soluble iron porphyrin (Fe(4-TMPyP)) and DNAtemplate, where PADDA (poly(acrylamide-co-diallyldimethylammonium chloride) isemployed as a co-immobilizing polymer. Cyclic voltammetry of FePyDP film showed a pairof reversible FeIII/FeII redox peaks and an irreversible FeIV/FeIII peak at –0.13 V and 0.89vs. Ag|AgCl in pH 7.4 PBS, respectively. An excellent catalytic reduction of NO wasdisplayed at –0.61 V vs. Ag|AgCl at a FePyDP film modified electrode.Chronoamperometric experiments demonstrated a rapid response to the reduction of NOwith a linear range from 0.1 to 90 μM and a detection limit of 30 nM at a signal-to-noiseratio of 3. On the other hand, it is the first time to apply high-valent iron porphyrin ascatalyst at modified electrode for NO catalytic oxidation at 0.89 vs. Ag|AgCl. The sensorshows a high selectivity of some endogenous electroactive substances in biological systems.The mechanism of response of the sensors to NO is preliminary studied. Full article
(This article belongs to the Special Issue Papers presented at I3S2004, Nanjing)

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