Relevant bibliographies by topics / Electrodes, Oxide

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Electrodes, Oxide'

Author: Grafiati
Published: 4 June 2021
Last updated: 27 January 2023

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Journal articles on the topic "Electrodes, Oxide"

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Tanumihardja, Esther, Douwe S. de Bruijn, Rolf H. Slaats, Wouter Olthuis, and Albert van den Berg. "Monitoring Contractile Cardiomyocytes via Impedance Using Multipurpose Thin Film Ruthenium Oxide Electrodes." Sensors 21, no. 4 (February 18, 2021): 1433. http://dx.doi.org/10.3390/s21041433.

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A ruthenium oxide (RuOx) electrode was used to monitor contractile events of human pluripotent stem cells-derived cardiomyocytes (hPSC-CMs) through electrical impedance spectroscopy (EIS). Using RuOx electrodes presents an advantage over standard thin film Pt electrodes because the RuOx electrodes can also be used as electrochemical sensor for pH, O2, and nitric oxide, providing multisensory functionality with the same electrode. First, the EIS signal was validated in an optically transparent well-plate setup using Pt wire electrodes. This way, visual data could be recorded simultaneously. Frequency analyses of both EIS and the visual data revealed almost identical frequency components. This suggests both the EIS and visual data captured the similar events of the beating of (an area of) hPSC-CMs. Similar EIS measurement was then performed using the RuOx electrode, which yielded comparable signal and periodicity. This mode of operation adds to the versatility of the RuOx electrode’s use in in vitro studies.
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HO, M. Y., P. S. KHIEW, D. ISA, T. K. TAN, W. S. CHIU, and C. H. CHIA. "A REVIEW OF METAL OXIDE COMPOSITE ELECTRODE MATERIALS FOR ELECTROCHEMICAL CAPACITORS." Nano 09, no. 06 (August 2014): 1430002. http://dx.doi.org/10.1142/s1793292014300023.

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With the emerging technology in the 21st century, which requires higher electrochemical performances, metal oxide composite electrodes in particular offer complementary properties of individual materials via the incorporation of both physical and chemical charge storage mechanism together in a single electrode. Numerous works reviewed herein have identified a wide variety of attractive metal oxide-based composite electrode material for symmetric and asymmetric electrochemical capacitors. The focus of the review is the detailed literature data and discussion regarding the electrochemical performance of various metal oxide composite electrodes fabricated from different configurations including binary and ternary composites. Additionally, projection of future development in hybrid capacitor coupling lithium metal oxides and carbonaceous materials are found to obtain significantly higher energy storage than currently available commercial electrochemical capacitors. This review describes the novel concept of lithium metal oxide electrode materials which are of value to researchers in developing high-energy and enhanced-cyclability electrochemical capacitors comparable to Li -ion batteries. In order to fully exploit the potential of metal oxide composite electrode materials, developing low cost, environment-friendly nanocomposite electrodes is certainly a research direction that should be extensively investigated in the future.
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Schlack, Sebastian, Hendrik Wulfmeier, and Holger Fritze. "Impact of electrode conductivity on mass sensitivity of piezoelectric resonators at high temperatures." Journal of Sensors and Sensor Systems 11, no. 2 (November 15, 2022): 299–313. http://dx.doi.org/10.5194/jsss-11-299-2022.

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Abstract. High-temperature stable piezoelectric Ca3TaGa3Si2O14 and La3Ga5SiO14 resonators with keyhole-shaped Pt electrodes are coated with metal oxide films such as TiO2−δ and SnO2 that overlap the Pt electrodes. The resonators are exposed to reducing atmospheres in order to increase the electrical conductivity of the oxide film and then act as extended oxide electrodes. The resulting increase in the effective electrode radius causes an increase in the mass sensitivity of the resonators and, thereby, resonance frequency shifts. In other words, the effective mass of the Pt electrode becomes higher. An electrical circuit model is presented to describe the increase in the effective electrode radius of the resonator, which is used to calculate the related resonance frequency shift. Additionally, an electromechanical model is presented, which subdivides the resonator into two coupled oscillators. One is representing the resonator volume underneath the Pt electrode and the other underneath the oxide electrode at increased electrical conductivity. The model reflects how the oxide electrodes affect the resonance frequency. Furthermore, the impact of increasing oxide electrode conductivity on the resonance frequency is discussed with respect to the application of oxide electrodes and for gas sensing.
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Ho, Mui Yen, Poi Sim Khiew, Dino Isa, and Wee Siong Chiu. "Electrochemical studies on nanometal oxide-activated carbon composite electrodes for aqueous supercapacitors." Functional Materials Letters 07, no. 06 (December 2014): 1440012. http://dx.doi.org/10.1142/s1793604714400128.

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In present study, the electrochemical performance of eco-friendly and cost-effective titanium oxide ( TiO 2)-based and zinc oxide-based nanocomposite electrodes were studied in neutral aqueous Na 2 SO 3 electrolyte, respectively. The electrochemical properties of these composite electrodes were studied using cyclic voltammetry (CV), galvanostatic charge–discharge (CD) and electrochemical impedance spectroscopy (EIS). The experimental results reveal that these two nanocomposite electrodes achieve the highest specific capacitance at fairly low oxide loading onto activated carbon (AC) electrodes, respectively. Considerable enhancement of the electrochemical properties of TiO 2/AC and ZnO /AC nanocomposite electrodes is achieved via synergistic effects contributed from the nanostructured metal oxides and the high surface area mesoporous AC. Cations and anions from metal oxides and aqueous electrolyte such as Ti 4+, Zn 2+, Na + and [Formula: see text] can occupy some pores within the high-surface-area AC electrodes, forming the electric double layer at the electrode–electrolyte interface. Additionally, both TiO 2 and ZnO nanoparticles can provide favourable surface adsorption sites for [Formula: see text] anions which subsequently facilitate the faradaic processes for pseudocapacitive effect. These two systems provide the low cost material electrodes and the low environmental impact electrolyte which offer the increased charge storage without compromising charge storage kinetics.
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Chuma, Takeshi, Haruhiko Toda, Morihiro Saito, Jun Kuwano, and Hidenobu Shiroishi. "Oxygen Reduction Electrode Properties of Perovskite-Related Oxides Sr(Fe,Co,Ru)O3-δ at Low Temperatures." Key Engineering Materials 320 (September 2006): 243–46. http://dx.doi.org/10.4028/www.scientific.net/kem.320.243.

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The O2-gas electrode (OGE) properties of the perovskite-related oxides SrFe1-x-yCoyRuxO3 (SFCR) were examined with the solid-state cells of the type (SFCR | Ba0.975Ce0.8Gd0.2O3 | SFCR) below 300°C. The SrFe0.7Co0.2Ru0.1O3 electrode showed the best OGE properties of the other SrFe1-x-yCoyRuxO3 (x0.2) electrodes prepared here. An oxide-ion current of 200 μA/cm2 was allowed to flow through the cell with the SFCR electrode at 225°C. The SFCR electrodes including some other compositions can be used instead of conventional Pt electrodes in solid-state cells at temperatures below 300°C.
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Gaire, Madhu, Najma Khatoon, and Douglas Chrisey. "Preparation of Cobalt Oxide–Reduced Graphitic Oxide Supercapacitor Electrode by Photothermal Processing." Nanomaterials 11, no. 3 (March 12, 2021): 717. http://dx.doi.org/10.3390/nano11030717.

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We report a photonic technique to instantaneously synthesize cobalt oxide reduced graphitic oxide (CoOx-rGO) supercapacitor electrodes. The electrode processing is achieved through rapidly heating the precursor material by irradiation of high-energy pulsed mostly visible light from a xenon lamp. Due to the short duration of the light pulse, we prepared the electrodes at room temperature instantaneously (ms), thus eliminating the several hours of processing times of the conventional techniques. The as-prepared electrodes exhibited a highly porous morphology, allowing for enhanced ionic transport during electrochemical interactions. The electrochemical properties of the CoOx-rGO electrodes were studied in 1 M KOH aqueous electrolyte. The non-rectangular cyclic voltammetry (CV) curves with characteristic redox peaks indicated the pseudocapacitive charge storage mechanism of the electrodes. From the discharge curves at 0.4 mA/cm2 and 1.6 A/g constant current densities, the electrode showed areal specific capacitance of 17 mF/cm2 and specific capacitance of 69 F/g, respectively. Cyclic stability was tested by performing 30,000 galvanostatic charge–discharge (GCD) cycles and the electrode exhibited 65% capacitance retention, showing its excellent electrochemical performance and ultra-long cycle life. The excellent electrochemical electrode properties are attributed to the unique processing technique, optimum processing parameters, improved conductivity due to the presence of rGO, and highly porous morphology which offers a high specific surface area. The novel photonic processing we report allows for high-temperature heating of the precursor films achieved via non-radiative recombination of photogenerated electron holes pairs during irradiation. Such extremely quick (ms) heating followed by instantaneous cooling results in the formation of a dense and robust bottom layer of the electrode, resulting in a long cycle life.
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Son, Seong Ho, Do Won Chung, and Won Sik Lee. "Development of Noble Metal Oxide Electrode for Low Oxygen Evolution." Advanced Materials Research 47-50 (June 2008): 750–53. http://dx.doi.org/10.4028/www.scientific.net/amr.47-50.750.

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In the electroplating and water treatment fields, as the demand and expectation on an electrode with high productivity and high efficiency are getting increased, various electrodes(DSE) with higher reactivity and durability are being developed. This study is intended to analyze the characteristics of the produced electrodes and to establish the optimum manufacturing conditions for electrode being used that we mentioned. For improving the durability, the changes of reactivity and corrosion resistance are observed as adding Tantalum and/or another components (hereafter stated as “α”) and surface treatment of substrate(Ti). As a result, increasing the amount of Iridium, the reactivity of electrode increased, and increasing amount of Tantalum, the durability of electrode increased. And thus, it is found out that Iridium and Tantalum have the opposite role each on the electrode’s reactivity and durability. And adding α and surface treatment substrate, an electrode with excellent reactivity and durability and low oxygen evolution can be manufactured. In the water treatment field like sterilizing in a swimming pool and power-plant cooling water, the high efficiency of sodium-hypochlorite generation is surely guaranteed.
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Cirocka, Anna, Dorota Zarzeczańska, and Anna Wcisło. "Good Choice of Electrode Material as the Key to Creating Electrochemical Sensors—Characteristics of Carbon Materials and Transparent Conductive Oxides (TCO)." Materials 14, no. 16 (August 22, 2021): 4743. http://dx.doi.org/10.3390/ma14164743.

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The search for new electrode materials has become one of the goals of modern electrochemistry. Obtaining electrodes with optimal properties gives a product with a wide application potential, both in analytics and various industries. The aim of this study was to select, from among the presented electrode materials (carbon and oxide), the one whose parameters will be optimal in the context of using them to create sensors. Electrochemical impedance spectroscopy and cyclic voltammetry techniques were used to determine the electrochemical properties of the materials. On the other hand, properties such as hydrophilicity/hydrophobicity and their topological structure were determined using contact angle measurements and confocal microscopy, respectively. Based on the research carried out on a wide group of electrode materials, it was found that transparent conductive oxides of the FTO (fluorine doped tin oxide) type exhibit optimal electrochemical parameters and offer great modification possibilities. These electrodes are characterized by a wide range of work and high chemical stability. In addition, the presence of a transparent oxide layer allows for the preservation of valuable optoelectronic properties. An important feature is also the high sensitivity of these electrodes compared to other tested materials. The combination of these properties made FTO electrodes selected for further research.
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Rossini, Matteo, Fabrizio Ganci, Claudio Zanca, Bernardo Patella, Giuseppe Aiello, and Rosalinda Inguanta. "Nanostructured Lead Electrodes with Reduced Graphene Oxide for High-Performance Lead–Acid Batteries." Batteries 8, no. 11 (November 3, 2022): 211. http://dx.doi.org/10.3390/batteries8110211.

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Nanostructured Pb electrodes consisting of nanowire arrays were obtained by electrodeposition, to be used as negative electrodes for lead–acid batteries. Reduced graphene oxide was added to improve their performances. This was achieved via the electrochemical reduction of graphene oxide directly on the surface of nanowire arrays. The electrodes with and without reduced graphene oxide were tested in a 5 M sulfuric acid solution using a commercial pasted positive plate and an absorbed glass mat separator in a zero-gap configuration. The electrodes were tested in deep cycling conditions with a very low cut-off potential. Charge–discharge tests were performed at 5C. The electrode with reduced graphene oxide outperformed the electrode without reduced graphene oxide, as it was able to work with a very high utilization of active mass and efficiency. A specific capacity of 258 mAhg−1–very close to the theoretical one–was achieved, and the electrode lasted for more than 1000 cycles. On the other hand, the electrode without reduced graphene oxide achieved a capacity close to 230 mAhg−1, which corresponds to a 90% of utilization of active mass.
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Barnett, Scott A. "(High-Temperature Energy, Materials, & Processes Division Outstanding Achievement Award Address) Mechanisms of Oxide Exsolution and Electrode Applications in Solid Oxide Cells." ECS Meeting Abstracts MA2022-02, no. 47 (October 9, 2022): 1769. http://dx.doi.org/10.1149/ma2022-02471769mtgabs.

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Solid oxide cell fuel electrodes based on perovskite oxides are desirable to avoid problems with Ni-based anodes, including coking in hydrocarbon fuels and degradation due to fuel impurities or redox cycling. However, oxide anode electrochemical performance is often lacking, limited by surface processes such as the dissociative adsorption of hydrogen. One way to improve such anodes is by the addition of a reducible cation in the oxide formulation, resulting in cation exsolution and nucleation of metallic nanoparticles on oxide surfaces during cell startup and operation. For example, substitution of small amounts of Ni or Ru on the B-site of Sr(Ti,Fe)O3 results in the formation of Ni-Fe or Ru-Fe nanoparticles, respectively, during exposure of the electrode to fuel during cell operation. This talk will examine the microstructural evolution of these exsolution anodes, making use of in situ x-ray diffraction measurements to detect formation of exsolved metal alloys and oxide phase changes. Exsolved metal nanoparticles enhance electrochemical performance, usually by promoting hydrogen dissociation on electrode surfaces. Changes in perovskite stoichiometry resulting from B-site exsolution can also impact the phase stability of the oxide, in some cases resulting in the formation of Ruddlesden-Popper phases that deleteriously affect electrochemical performance. The application of exsolution in fuel electrodes in novel thin-electrolyte oxygen-electrode-supported cells is discussed; the results indicate that performance in H2/H2O fuel is superior to Ni-YSZ in both electrolysis and fuel cell modes. Electrochemical characteristics of the exsolution electrodes are especially superior to Ni-YSZ when operated in CO/CO2 fuel.
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Dissertations / Theses on the topic "Electrodes, Oxide"

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Nwosu, Nkem O. E. "Optimisation of electroless co-deposited solid oxide fuel cell electrodes." Thesis, Edinburgh Napier University, 2013. http://researchrepository.napier.ac.uk/Output/6448.

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Research already carried out on the use of the recently patented electroless nickel ceramic codeposition technique as a method of manufacturing solid oxide fuel cell (SOFC) electrodes has thus far indicated that, while functional electrodes can be manufactured by the technique, for optimum performance of the cell, amplification of the ceramic content of the coatings is still required. By mainly employing external agents such as surface active agents (surfactants) and magnetic fields (in a bid to aid ceramic particle stability), this research focused on the prospect of increasing the ceramic content of cermets co-deposited for use as SOFC electrodes. A total of 137 co-deposited samples were produced from different bath compositions. As a prelude to the study, the interactions between the ceramic powders used (yttria stabilised zirconia (YSZ) / lanthanum strontium manganate (LSM)) and the medium for the deposition process – the electroless nickel solution, were investigated by zeta potentiometry and ultraviolet-visible spectroscopy techniques. The results obtained from the studies led to a variation of a series of fundamental plating factors such as the ceramic bath loading and particle size of the powders. While the former was found to yield the highest ceramic content in the coating at a bath loading of 50 g/l, variation of latter notably produced mixed results. With the introduction of surfactants, it was noted that above the surfactant's (sodium dodecyl sulphate) critical micelle concentration, the incorporation of ceramic particles (YSZ) into the nickel matrix steadily increased to as much as 60 volume %. An inverse relationship was though found to exist between the coating thickness and the surfactant's bath concentration. Uniform coatings were found to be associated with low magnetic field strengths while although increased magnetic field strengths positively resulted in the amplification of particle incorporation into the coating, a lack of cohesion between the coating and the substrate – as indicated by coating flake-off, was observed at such strengths. It is suggested that because the magnetic flux was more dominant than the normally ionic plating mechanism, the particles co-deposited under the influence of a high magnetic field were relatively unstable after the coating process. Since LSM is alkaline in nature this work confirms that future research on the application of electroless nickel ceramic co-deposition as a method of manufacturing SOFC cathodes, be focused on the use of alkaline electroless nickel baths rather than the acidic solutions, which better suite YSZ particles.
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Astuti, Yeni. "Bio-functionalised nanostructured metal oxide electrodes." Thesis, Imperial College London, 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.429459.

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Makgae, Mosidi Elizabeth. "Environmental electrochemistry of organic compounds at metal oxide electrodes." Thesis, Stellenbosch : Stellenbosch University, 2004. http://hdl.handle.net/10019.1/49947.

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Dissertation (PhD)--Stellenbosch University, 2004.
ENGLISH ABSTRACT: This study investigates the electrochemical oxidation of phenol. Phenol is a major toxin and water pollutant. In addition, during water treatment it reacts with chlorine to produce carcinogenic chlorophenols. lts treatment down to trace levels is therefore of increasing concern. For this purpose, dynamically stable anodes for the breakdown of phenols to carbon dioxide or other less harmful substances were developed and characterized. The anodes were prepared from mixed oxides of tin (Sn) and the precious metals ruthenium (Ru), tantalum (Ta) and iridium (Ir), which in tum were prepared using sol-gel techniques. This involved dip-coating the aqueous salts of the respective metals onto titanium substrates and heating to temperatures of several hundreds of degree Celsius. The properties of these mixed oxide thin films were investigated and characterized using thermal gravimetric analysis (TGA), scanning electron microscopy (SEM), atomic force microscopy (AFM), elemental dispersive energy X-ray analysis (EDX), X-ray diffraction (XRD), Rutherford backscattering spectrometry (RBS), particle induced X-ray emission (PIXE) and electrochemical measurements. A variety of different electrode materials including Til Sn02-Ru02-Ir02, Ti/Ta20s-Ir02 and Ti/RhOx-Ir02 were developed and tested for their potential as oxidation catalysts for organic pollutants in wastewaters. Depending on the anode type, phenol was found to be electrochemically degraded, to different extents, on these surfaces during electrolysis. It was however found that the oxidation rate not only depended on the chemical composition but also on the oxide morphology revealed, resulting from the preparation procedure. The Ti/SnOz-Ru02-Ir02 film was found to be the most efficient surface for the electrolytic breakdown of phenol. This film oxidized phenol at a potential of 200 mV vs Ag/AgC!. The activity of the catalytic systems was evaluated both on the basis of phenol removal efficiency as well as the kinetics of these reactions. Phenol removal efficiency was more than 90% for all the film surfaces prepared and the rate of the reaction followed first order kinetics. A pathway for the electrochemical degradation of phenol was derived using techniques such as HPLC to identify the breakdown products. These pathway products included the formation of benzoquinone and the further oxidation of benzoquinone to the carboxylic acids malic, malonic and oxalic.
AFRIKAANSE OPSOMMING: Die onderwerp van hierdie studie is die elektrochemiese oksidasie van fenol deur nuwe gemengde-oksied elektrodes. Fenol is 'n belangrike gifstof en besoedelingsmiddel in water. Daarbenewens kan fenolook met chloor reageer tydens waterbehandeling om sodoende karsinogeniese chlorofenole te vorm. Dit is dus belangrik dat metodes ondersoek word wat die konsentrasie van fenol in water verminder. Hierdie studie behels die bereiding en karakterisering van nuwe dinamiese stabiele anodes (DSA) vir die afbreek van fenol tot koolstofdioksied en ander minder gevaarlike verbindings. Hierdie nuwe anodes is berei vanaf die gemengde-okside van die edelmetale tin (Sn), ruthenium (Ru), tantalum (Ta) en iridium (Ir), met behulp van sol-gel tegnieke. Die finale stap in die bereiding behels kalsinering van die oksides by temperature van "n paar honderd grade Celsius. Hierdie nuwe elektrodes is later gebruik om die oksidasie van fenol te evalueer. Die gemengde-oksied dunlae/anodes IS d.m.v. die volgende analitiesetegnieke gekarakteriseer: termiese-gravimetriese analise (TGA), skandeerelektronmikroskopie (SEM), atoomkragmikroskopie (AFM), elementverstrooiingsenergie- X-straalanalise (EDX), X-straaldiffraksie (XRD), Rutherford terug-verstrooiingspektroskopie (RBS), partikel-geinduseerde X-straal emissie (PIXE), en elektrochemiese metings. 'n Verskeidenheid elektrodes van verskillende materiale is berei en hul potensiaal as oksidasie-kataliste vir organiese besoedelingsmiddels in afloopwater bepaal. Hierdie elektrodes het die volgende ingesluit: Ti/Sn02-Ru02-Ir02, Ti/Ta20s-Ir02 en Ti/RhOx-Ir02. Gedurende elektrolise is fenol elektrochemies afgebreek tot verskillende vlakke, afhangende van die tipe elektrode. Die oksidasietempo het egter nie alleen van die chemiese samestelling van die elektrode afgehang nie, maar ook van die morfologie van die okside, wat op hulle beurt van die voorbereidingsprosedure afgehang het. Daar is bevind dat die Ti/Sn02-Ru02-Ir02 elektrode die mees effektiewe oppervlakke vir die afbreek van fenol is. Hier het die oksidasie van fenol by 'n potensiaal van 200 mV plaasgevind. Die aktiwiteite van die katalitiese sisteme IS bepaal op grond van hulle fenolverwyderingsdoeltreffendheid. Die kinetika van die reaksies is ook bepaal. Al die elektrodes het >90% fenolverwyderingsdoeltreffendheid getoon en die reaksietempos was van die eerste-orde. Deur van analitiese tegnieke soos hoëdrukvloeistofchromatografie (HPLC) gebruik te maak is die afbreekprodukte van fenol geïdentifiseer en 'n skema vir die elektrochemiese afbreek van fenol uitgewerk. Daar is bevind dat bensokinoon gevorm het, wat later oksidasie ondergaan het om karboksielsure te vorm.
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Hernández, Rodríguez Elba María. "Solid Oxide Electrolysis Cells electrodes based on mesoporous materials." Doctoral thesis, Universitat de Barcelona, 2018. http://hdl.handle.net/10803/665269.

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The need of substituting the current energetic model by a system based on clean Renewable Energy Sources (RES) have gained more importance in the last decades due to the environmental issues related to the use of fossil fuels. These energy sources are site-specific and intermittent, what makes essential the development of Energy Storage Systems (ESS) that allows the storage of the electricity generated by renewable energies. Among the technologies under development for the storage of electrical energy, Solid Oxide Electrolysis Cells (SOECs) have been proposed in the last decades as a promising technology. Achieving efficiencies higher than 85%, SOEC technology is able to convert electrical energy into chemical energy through the reduction of H2O, CO2 or the combination of both; generating H2, CO or syngas (H2 +CO). The implementation of this technology based on renewable electrical energy, combined with fuel cells would allow closing the carbon cycle. The work presented in this thesis has been devoted to enhance the performance of SOEC. The approach that is presented for that propose is based on the implementation of high surface area and thermally stable mesoporous metal oxide materials on the fabrication of SOEC electrodes. High performance and stability of the electrodes was expected during its characterization. Structural and electrochemical characterization techniques have been applied during the development of this thesis for this purpose. The thesis is organized in eight chapters briefly described in the following: Chapter 1 briefly analyses the current energy scenario presenting electrolysers as a promising technology for the storage of electrical energy. Besides, basic principles of SOECs operation and the state-of-the-art materials of SOECs are reviewed. Chapter 2 describes all the experimental methods and techniques employed in this thesis for the synthesis and characterization of synthesised materials and fabricated cells. Chapter 3 presents the results obtained from the structural characterization of the mesoporous materials and fabricated electrodes, revealing the successful implantation of the hard-template method for obtaining Sm0.2Ce0.8O1.9 (SDC), Ce0.8Gd0.2O1.9 (CGO) and NiO mesoporous powders, and the fabrication of SDC-SSC (Sm0.5Sr0.5CoO3-δ), CGO- LSCF (La0.6Sr0.4Co0.2Fe0.8O3) and NiO-SDC electrodes based on mesoporous materials. The attachment of the mesoporous scaffold for the fabrication of oxygen electrodes has been optimized at 900 °C. Chapter 4 compares electrolyte- and fuel electrode-supported cell configurations based on the same oxygen electrode. The electrochemical performance and the microstructural characterization of these cells are considered for that purpose. Showing a maximum current density of -0.83 and -0.81 A/cm2 on electrolysis and co- electrolysis modes respectively, fuel electrode-supported cells are considered more suitable for SOEC fabrication. Chapter 5 presents a study focused on analysing the influence of the oxygen electrode interface on the SOEC performance. The electrochemical and microstructural characterization of barrier layers and oxygen electrodes fabricated applying different methods are discussed in this chapter. The combination of a barrier layer fabricated by Pulsed Laser Deposition (PLD) with an oxygen electrode based on mesoporous materials resulted on the injection of up to -1 A/cm2, what allows concluding that this interface microstructure is directed related with the best performing SOECs in this thesis. Chapter 6 shows the performance of SOEC cells on co-electrolysis mode containing the optimized oxygen electrode, fabricated by infiltration of mesoporous scaffolds. The long-term stability of infiltrated mesoporous composites have been demonstrated during 1400 h, registering degradation rates of 2%/kh and <1%/kh when current densities of -0.5 A/cm2 and -0.75 A/cm2 are injected, respectively. Chapter 7 shows results of the scale-up of the mesoporous-based electrodes for the fabrication of large area cells. Their electrochemical performance shows high fuel flexibility, injecting -0.82 A/cm2 on co-electrolysis mode; and long-term stability injecting -0.5 A/cm2 for 600 h. The conclusions of this thesis are presented in Chapter 8.
Una de las principales desventajas de las fuentes de energías renovables es que producen energía eléctrica de forma discontinua. Los electrolizadores de alta temperatura basados en óxidos sólidos (SOEC) se presentan como una tecnología prometedora para el almacenamiento de energía eléctrica. Alcanzando eficiencias mayores de un 85%, los electrolizadores SOEC permite convertir energía eléctrica en energía química mediante la reducción de las moléculas de agua (H2O), dióxido de carbono (CO2), o la combinación de ambas; generándose hidrógeno (H2), monóxido de carbono (CO) o gas de síntesis (H2 +CO) como producto. El trabajo que se presenta en esta tesis tiene como objetico mejorar el rendimiento de los electrolizadores SOEC mediante la utilización de óxidos metálicos mesoporosos, caracterizados por poseer alta área superficial y ser estables a altas temperaturas. Esta tesis está organizada en ocho capítulos. Los capítulos 3, 4, 5, 6 y 7 presentan los resultados alcanzados: El capítulo 3 presenta la caracterización estructural de los materiales mesoporosos y de los electrodos fabricados. Además, la temperatura de adhesión del material mesoporoso ha sido optimizada y se ha fijado a 900 °C. El capítulo 4 compara electrolizadores fabricados soportados por el electrodo de combustible y por el electrolito. Los resultados muestran que las densidades de corriente más altas fueron inyectadas en los electrolizadores soportados por el electrodo de combustible, considerándose esta configuración la más apropiada. El capítulo 5 presenta la influencia de la microstructura de la intercara del electrodo de oxígeno en el rendimiento de los electrolizadores SOEC. La caracterización electroquímica, apoyada por la caracterización microestructural, ha demostrado que la máxima densidad de corriente ha sido inyectada por el electrolizador cuya barrera de difusión ha sido depositado por láser pulsado (PLD) y la capa funcional del electrodo de oxígeno mediante infiltración de materiales mesoporosos. El capítulo 6 estudia el electrodo de oxígeno optimizado. Durante 1400 h de operación continua y caracterización microstructural, se ha demostrado la estabilidad de este electrodo. Por último, el capítulo 7 muestra los resultados obtenidos del escalado de los electrodos mesoporosos en celdas de mayor área (25 cm2). La caracterización electroquímica muestra alta flexibilidad ante las composiciones de gases utilizadas, y estabilidad de los electrodos mesoporosos propuestos.
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Koep, Erik Kenneth. "A Quantitative Determination of Electrode Kinetics using Micropatterned Electrodes." Diss., Georgia Institute of Technology, 2006. http://hdl.handle.net/1853/10524.

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Interfacial polarization resistances limit the performance of many thin film solid-state devices, especially at low temperatures. To improve performance, a fundamental understanding of the electrode kinetics that govern interfacial reaction rates must be developed. The goal of this work is to determine site-specific reaction mechanisms and the relative significance of various reactions in order to quantify optimum structural parameters within the cathode microstructure. Key parameters include the length of triple phase boundary (TPB), the quantity of exposed electrolyte/electrode surface, and the ratio of electrolyte to electrode material. These parameters, when studied in a specific system, can be incorporated into broader models, which will encompass the specific conductivity of each component to develop an optimized three-dimensional network. The emphasis of this work is the systematic control and manipulation of potential cathodic reaction sites in order to develop an understanding of the relative importance of specific reaction sites. Since the physical dimensions of reaction sites are relatively small, an approach has been developed that utilizes micro-fabrication (similar to that used in integrated-circuit fabrication) to produce small and highly controlled microstructures. Investigations were made into the nature and reactivity of Triple Phase Boundaries (hereafter TPB) through the use of patterned platinum electrodes since only the TPBs are active in these electrodes. After the processing details of micro-fabrication were established for the platinum electrodes, patterned Mixed-Ionic/Electronic Conducting (MIEC) electrodes were fabricated and studied using impedance spectroscopy to determine the contributions from the MIEC surface versus the TPB. Systematically changing the geometry of the MIEC electrodes (thickness and line width) allowed for the determination of the effect of ambipolar transport within the MIEC on the activity of MIEC surfaces versus the TPB. This information is critical to rational design of functionally graded electrodes (with optimal particle size, shape, porosity and conductivity). In addition to experimental studies, representative patterned electrode samples were made available for collaborative studies with surface scientists at other institutions to provide additional techniques (such as Raman Spectroscopy) on the carefully designed and controlled cathode surfaces.
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Baez, Baez Victor Antonio. "Metal oxide coated electrodes for oxygen reduction." Thesis, University of Southampton, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.241271.

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Graves, John Edward. "The electrochemistry of titanium oxide ceramic electrodes." Thesis, University of Southampton, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.305486.

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MacDonald, Gordon Alex. "Nanoscale Characterization of the Electrical Properties of Oxide Electrodes at the Organic Semiconductor-Oxide Electrode Interface in Organic Solar Cells." Diss., The University of Arizona, 2015. http://hdl.handle.net/10150/347338.

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This dissertation focuses on characterizing the nanoscale and surface averaged electrical properties of transparent conducting oxide (TCO) electrodes such as indium tin oxide (ITO) and transparent metal-oxide (MO) electron selective interlayers (ESLs), such as zinc oxide (ZnO), the ability of these materials to rapidly extract photogenerated charges from organic semiconductors (OSCs) used in organic photovoltaic (OPV) cells, and evaluating their impact on the power conversion efficiency (PCE) of OPV devices. In Chapter 1, we will introduce the fundamental principles regarding the need for low cost power generation, the benefits of OPV technologies, as well as the key principles that govern the operation of OPV devices and the key innovations that have advanced this technology. In Chapter 2 of this dissertation, we demonstrate an innovative application of conductive probe atomic force microscopy (CAFM) to map the nanoscale electrical heterogeneity at the interface between an electrode, such as ITO, and an OSC such as the p-type OSC copper phthalocyanine (CuPc).(MacDonald et al. (2012) ACS Nano, 6, p. 9623) In this work we collected arrays of J-V curves, using a CAFM probe as the top contact of CuPc/ITO systems, to map the local J-V responses. By comparing J-V responses to known models for charge transport, we were able to determine if the local rate-limiting step for charge transport is through the OSC (ohmic) or the CuPc/ITO interface (nonohmic). These results strongly correlate with device PCE, as demonstrated through the controlled addition of insulating alkylphosphonic acid self-assembled monolayers (SAMs) at the ITO/CuPc interface. Subsequent chapters focus on the electrical property characterization of RF-magnetron sputtered ZnO (sp-ZnO) ESL films on ITO substrates. We have shown that the energetic alignment of ESLs and the organic semiconducting (OSC) active materials plays a critical role in determining the PCE of OPV devices and the appearance of, or lack thereof, UV light soaking sensitivity. For ZnO and fullerene interfaces, we have shown that either minimizing the oxygen partial pressure during ZnO deposition or exposure of ZnO to UV light minimizes the energetic offset at this interface and maximizes device PCE. We have used a combination of device testing, device modeling, and impedance spectroscopy to fully characterize the effects that energetic alignment has on the charge carrier transport and charge carrier distribution within the OPV device. This work can be found in Chapter 3 of this dissertation and is in preparation for publication. We have also shown that the local properties of sp-ZnO films varies as a function of the underlying ITO crystal face. We show that the local ITO crystal face determines the local nucleation and growth of the sp-ZnO films. We demonstrate that this effects the morphology, the chemical resistance to etching as well as the surface electrical properties of the sp-ZnO films. This is likely due to differences in the surface mobility of sputtered Zn and O atoms on these crystal faces during film nucleation. This affects the nanoscale distribution of electrical and chemical properties. As a result we demonstrate that the PCE, and UV sensitivity of the J-V response of OPVs using sp-ZnO ESLs are strongly impacted by the distribution of ITO crystal faces at the surface of the substrate. This work can be found in Chapter 4 of this dissertation and is in preparation for publication. These studies have contributed to a detailed understanding of the role that electrical heterogeneity, insulating barriers and energetic alignment at the MO/OSC interface play in OPV PCE.
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Liu, Yujing. "Nanostructured transparent conducting oxide electrodes through nanoparticle assembly." Diss., lmu, 2012. http://nbn-resolving.de/urn:nbn:de:bvb:19-149076.

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Baker, Priscilla G. L. "Sol-gel preparation, characterisation and electrochemistry of mixed metal tin oxide electrodes." Thesis, Stellenbosch : Stellenbosch University, 2004. http://hdl.handle.net/10019.1/50096.

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Books on the topic "Electrodes, Oxide"

1

Sato, Norio. Electrochemistry at metal and semiconductor electrodes. Amsterdam: Elsevier, 1998.

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Haschke, Sandra. Electrochemical Water Oxidation at Iron(III) Oxide Electrodes. Wiesbaden: Springer Fachmedien Wiesbaden, 2015. http://dx.doi.org/10.1007/978-3-658-09287-0.

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International Conference on Oxide Materials for Electronic Engineering--Fabrication, Properties and Applications (2012 Lʹviv, Ukraine). Oxide materials for electronic engineering: Fabrication, properties and applications : selected, peer reviewed papers from the International Scientific Conference on Oxide Materials for Electronic Engineering - Fabrication, Properties and Applications (OMEE 2012), September 3-7, 2012, Lviv, Ukraine. Durnten-Zurich, Switzerland: TTP, Trans Tech Publications Ltd, 2013.

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S, Licht, ed. Semiconductor electrodes and photoelectrochemistry. Weinheim: Wiley-VCH, 2002.

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Jacek, Lipkowski, and Ross P. N, eds. Adsorption of molecules at metal electrodes. New York, NY: VCH, 1992.

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International Symposium on Solid Oxide Fuel Cells (10th 2007 Nara, Japan). Solid oxide fuel cells 10: (SOFC-X). Edited by Eguchi K and Electrochemical Society. Pennington, N.J: Electrochemical Society, 2007.

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International Symposium on Solid Oxide Fuel Cells (6th 1999 Honolulu, Hawaii). Solid oxide fuel cells: (SOFC VI) : proceedings of the Sixth International Symposium. Edited by Singhal Subhash C, Dokiya M, Electrochemical Society. High Temperature Materials Division., Electrochemical Society Battery Division, and SOFC Society of Japan. Pennington, NJ: Electrochemical Society, 1999.

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Szklarczyk, Marek. Fotokataliza na elektrodach półprzewodnikowych. Warszawa: Wydawnictwa Uniwersytetu Warszawskiego, 1990.

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Lluís, Miribel-Català Pere, and SpringerLink (Online service), eds. A CMOS Self-Powered Front-End Architecture for Subcutaneous Event-Detector Devices: Three-Electrodes Amperometric Biosensor Approach. Dordrecht: Springer Science+Business Media B.V., 2011.

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Ama, Onoyivwe Monday, and Suprakas Sinha Ray, eds. Nanostructured Metal-Oxide Electrode Materials for Water Purification. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-43346-8.

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Book chapters on the topic "Electrodes, Oxide"

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Chiku, Masanobu. "Nickel Oxide Electrodes." In Encyclopedia of Applied Electrochemistry, 1366–68. New York, NY: Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4419-6996-5_512.

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Wirtz, G. P., and H. S. Isaacs. "Oxide Electrodes at High Temperatures." In Solid State Batteries, 483–87. Dordrecht: Springer Netherlands, 1985. http://dx.doi.org/10.1007/978-94-009-5167-9_36.

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Trasatti, Sergio. "Hydrogen Evolution on Oxide Electrodes." In Modern Chlor-Alkali Technology, 281–94. Dordrecht: Springer Netherlands, 1992. http://dx.doi.org/10.1007/978-94-011-2880-3_24.

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Ihlefeld, Jon F., Mark D. Losego, and Jon-Paul Maria. "Base Metal Bottom Electrodes." In Chemical Solution Deposition of Functional Oxide Thin Films, 571–92. Vienna: Springer Vienna, 2013. http://dx.doi.org/10.1007/978-3-211-99311-8_23.

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Kaur, Gurbinder. "Interaction of Glass Seals/Electrodes and Electrolytes." In Solid Oxide Fuel Cell Components, 315–74. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-25598-9_8.

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Mogensen, Mogens, and Peter Holtappels. "Ni-Based Solid Oxide Cell Electrodes." In Solid Oxide Fuels Cells: Facts and Figures, 25–45. London: Springer London, 2012. http://dx.doi.org/10.1007/978-1-4471-4456-4_2.

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Wroblowa, Halina S. "Rechargeable Manganese Oxide Electrodes and Cells." In Electrochemistry in Transition, 147–59. Boston, MA: Springer US, 1992. http://dx.doi.org/10.1007/978-1-4615-9576-2_11.

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Chukwuneke, Chikaodili, Joshua O. Madu, Feyisayo V. Adams, and Oluwagbenga T. Johnson. "Application of Metal Oxides Electrodes." In Nanostructured Metal-Oxide Electrode Materials for Water Purification, 127–49. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-43346-8_8.

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Niwa, Koichi, Jeffrey S. Cross, Mineharu Tsukada, Kazuaki Kurihara, and Nobuo Kamehara. "Properties of Fram Capacitors with Oxide Electrodes." In Ceramic Transactions Series, 311–17. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2012. http://dx.doi.org/10.1002/9781118408186.ch28.

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Fourcade, Julien, and Olivier Citti. "New Tin Oxide Electrodes for Glass Melting." In 73rd Conference on Glass Problems, 183–99. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118710838.ch14.

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Conference papers on the topic "Electrodes, Oxide"

1

Jadhav, S. L., A. L. Jadhav, V. S. Jamdade, K. R. Kharat, A. A. Deshmane, and A. V. Kadam. "Controlled Synthesis of Cobalt Oxide Electrode by Electrodeposition for Supercapacitor Application." In National Conference on Relevance of Engineering and Science for Environment and Society. AIJR Publisher, 2021. http://dx.doi.org/10.21467/proceedings.118.56.

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Cobalt oxide (Co3O4) electrodes were prepared on conductive stainless still (SS) substrate using cobalt nitrate as a cobalt source by implementing simple and cost-effective chemical electrodeposition method and here, characterized for structural and electrochemical analysis for supercapacitor applications. The effect of different deposition potential on capacitance and charging-discharging stability of cobalt oxide electrode were studied. X-ray diffractions confirms the face centered cubic crystal structure of Co3O4 electrodes. Electrochemical capacitive analysis of cobalt oxide electrode was studied in 1MKOH aqueous electrolyte solution. The observed maximum specific capacitance attained with cobalt oxide was 273.3 F/g at scan rate 5mV/s. The observed specific power, specific energy and coulomb efficiency were 12.12W/kg, 74.75 Wh/kg, and 99.63%, respectively. The cycling stability of the cobalt oxides shows 62% up to 500 cycles.
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Greene, Eric S., and Wilson K. S. Chiu. "Mass Transfer in Functionally Graded Solid Oxide Fuel Cell Electrodes." In ASME 2005 International Mechanical Engineering Congress and Exposition. ASMEDC, 2005. http://dx.doi.org/10.1115/imece2005-82531.

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A 1-D computational model is presented in which performance of a solid oxide fuel cell with functionally graded electrodes can be predicted. The model calculates operational cell voltages with varying geometric and operational parameters. The model accounts for losses from mass transport through the porous electrodes, ohmic losses from current flow through the electrodes and electrolyte, and activation polarization. It also includes a model for the full or partial internal reforming of methane. The model was applied to investigate the effect of electrode porosity distribution on performance. Specifically the physical phenomena that occur when the electrode is designed with a change in microstructure along its thickness is studied. The general trends that occur are investigated to find the arrangement for which the minimal polarization occurs. Both diluted hydrogen fuel and partially reformed methane streams are investigated. It is concluded that performance benefits are seen when the electrodes are given an increase in porosity near the electrolyte interface.
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Recknagle, Kurtis P., Emily M. Ryan, and Moe A. Khaleel. "Numerical Modeling of the Distributed Electrochemistry and Performance of Solid Oxide Fuels Cells." In ASME 2011 International Mechanical Engineering Congress and Exposition. ASMEDC, 2011. http://dx.doi.org/10.1115/imece2011-64232.

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A cell-level distributed electrochemistry (DEC) modeling tool has been developed to enable predicting trends in solid oxide fuel cell performance by considering the coupled and spatially varying multi-physics that occur within the tri-layer. The approach calculates the distributed electrochemistry within the electrodes, which includes the charge transfer and electric potential fields, ion transport throughout the tri-layer, and gas distributions within the composite and porous electrodes. The thickness of the electrochemically active regions within the electrodes is calculated along with the distributions of charge transfer. The DEC modeling tool can examine the overall SOFC performance based on electrode microstructural parameters, such as particle size, pore size, porosity, electrolyte- and electrode-phase volume fractions, and triple-phase-boundary length. Recent developments in electrode fabrication methods have lead to increased interest in using graded and nano-structured electrodes to improve the electrochemical performance of SOFCs. This paper demonstrates how the DEC modeling tool can be used to help design novel electrode microstructures by optimizing a graded anode for high electrochemical performance.
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Sohal, M. S., J. E. O’Brien, C. M. Stoots, V. I. Sharma, B. Yildiz, and A. Virkar. "Degradation Issues in Solid Oxide Cells During High Temperature Electrolysis." In ASME 2010 8th International Conference on Fuel Cell Science, Engineering and Technology. ASMEDC, 2010. http://dx.doi.org/10.1115/fuelcell2010-33332.

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Idaho National Laboratory (INL) is performing high-temperature electrolysis (HTE) research to generate hydrogen using solid oxide electrolysis cells (SOECs). The project goals are to address the technical and degradation issues associated with the SOECs. This paper provides a summary of ongoing INL and INL-sponsored activities aimed at addressing SOEC degradation. These activities include stack testing, post-test examination, degradation modeling, and issues that need to be addressed in the future. Major degradation issues relating to solid oxide fuel cells (SOFC) are relatively better understood than those for SOECs. Some of the degradation mechanisms in SOFCs include contact problems between adjacent cell components, microstructural deterioration (coarsening) of the porous electrodes, and blocking of the reaction sites within the electrodes. Contact problems include delamination of an electrode from the electrolyte, growth of a poorly (electronically) conducting oxide layer between the metallic interconnect plates and the electrodes, and lack of contact between the interconnect and the electrode. INL’s test results on HTE using solid oxide cells do not provide clear evidence as to whether different events lead to similar or drastically different electrochemical degradation mechanisms. Post-test examination of the SOECs showed that the hydrogen electrode and interconnect get partially oxidized and become nonconductive. This is most likely caused by the hydrogen stream composition and flow rate during cooldown. The oxygen electrode side of the stacks seemed to be responsible for the observed degradation because of large areas of electrode delamination. Based on the oxygen electrode appearance, the degradation of these stacks was largely controlled by the oxygen electrode delamination rate. Virkar et al. [19–22] have developed a SOEC model based on concepts in local thermodynamic equilibrium in systems otherwise in global thermodynamic nonequilibrium. This model is under continued development. It shows that electronic conduction through the electrolyte, however small, must be taken into account for determining local oxygen chemical potential within the electrolyte. The chemical potential within the electrolyte may lie out of bounds in relation to values at the electrodes in the electrolyzer mode. Under certain conditions, high pressures can develop in the electrolyte just under the oxygen electrode (anode)/electrolyte interface, leading to electrode delamination. This theory is being further refined and tested by introducing some electronic conduction in the electrolyte.
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Dias, N. S., A. F. Silva, P. M. Mendes, and J. H. Correia. "Non-invasive iridium oxide biopotential electrodes." In IECON 2009 - 35th Annual Conference of IEEE Industrial Electronics (IECON). IEEE, 2009. http://dx.doi.org/10.1109/iecon.2009.5414851.

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Chu, Sangwook, Konstantinos Gerasopoulos, and Reza Ghodssi. "Biotemplated hierarchical nickel oxide supercapacitor electrodes." In 2015 28th IEEE International Conference on Micro Electro Mechanical Systems (MEMS). IEEE, 2015. http://dx.doi.org/10.1109/memsys.2015.7051160.

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Ahmad, Mahmoud Al, and Shereen Hasan. "Stretchable ruthenium oxide nanoparticles coated electrodes." In 2016 18th Mediterranean Electrotechnical Conference (MELECON). IEEE, 2016. http://dx.doi.org/10.1109/melcon.2016.7495449.

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Chakraborty, Bitan, Alexandra Joshi-Imre, and Stuart F. Cogan. "Sputtered Ruthenium Oxide Neural Stimulation Electrodes." In 2021 43rd Annual International Conference of the IEEE Engineering in Medicine & Biology Society (EMBC). IEEE, 2021. http://dx.doi.org/10.1109/embc46164.2021.9630483.

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Kim-Lohsoontorn, P., H. B. Yim, and J. M. Bae. "Electrochemical Performance of Ni-YSZ, Ni/Ru-GDC, LSM-YSZ, LSCF and LSF Electrodes for Solid Oxide Electrolysis Cells." In ASME 2010 8th International Conference on Fuel Cell Science, Engineering and Technology. ASMEDC, 2010. http://dx.doi.org/10.1115/fuelcell2010-33017.

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The electrochemical performance of solid oxide electrolysis cells (SOECs) having nickel – yttria stabilized zirconia (Ni-YSZ) hydrogen electrode and a composite lanthanum strontium manganite – YSZ (La0.8Sr0.2MnO3−δ – YSZ) oxygen electrodes has been studied over a range of operating conditions temperature (700 to 900°C). Increasing temperature significantly increased electrochemical performance and hydrogen generation efficiency. Durability studies of the cell in electrolysis mode were made over 200 h periods (0.1 A/cm2, 800°C, and H2O/H2 = 70/30). The cell significantly degraded over the time (2.5 mV/h). Overpotentials of various SOEC electrodes were evaluated. Ni-YSZ as a hydrogen electrode exhibited higher activity in SOFC mode than SOEC mode while Ni/Ru-GDC presented symmetrical behavior between fuel cell and electrolysis mode and gave lower losses when compared to the Ni-YSZ electrode. All the oxygen electrodes gave higher activity for the cathodic reaction than the anodic reaction. Among the oxygen electrodes in this study, LSM-YSZ exhibited nearest to symmetrical behavior between cathodic and anodic reaction. Durability studies of the electrodes in electrolysis mode were made over 20–70 h periods. Performance degradations of the oxygen electrodes were observed (3.4, 12.6 and 17.6 mV/h for LSM-YSZ, LSCF and LSF, respectively). The Ni-YSZ hydrogen electrode exhibited rather stable performance while the performance of Ni/Ru-GDC decreased (3.4 mV/h) over the time. This was likely a result of the reduction of ceria component at high operating voltage.
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Ju, W. T., and S. H. Hong. "Development of Fabrication Processes for Tubular Solid Oxide Fuel Cell (SOFC) by Plasma Spraying." In ITSC 1998, edited by Christian Coddet. ASM International, 1998. http://dx.doi.org/10.31399/asm.cp.itsc1998p1067.

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Abstract The atmospheric pressure plasma spray processes for functional layers of the tubular solid oxide fuel cell are developed to build a fuel cell structure consisting of air electrode, ceramic electrolyte, and fuel electrode. Further more the characteristics of each film are also investigated. The layers of LSM (La0.65Sr0.35MnO3) air electrode and Ni/8YSZ fuel electrode have porosities of 23 ~32 % sufficient for supplying fuel and oxidant gases efficiently to electrochemical reaction interfaces. The measured electrical conductivities of the electrodes are higher than 90 S/cm at 1000 °C, which satisfy the requirement as the current collecting electrodes. The YSZ electrolyte film has a high ionic conductivity of 0.07 S/cm at 1000 °C, but shows a bit too porous to block the oxygen molecule penetration through it. A unit tubular SOFC is fabricated by the optimized plasma spray processes for depositing each functional film and forming a porous cylindrical supporting tube of the cell, and turns out to have a promising capability of electricity generation.
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Reports on the topic "Electrodes, Oxide"

1

Sholklapper, Tal Zvi. Nanostructured Solid Oxide Fuel Cell Electrodes. Office of Scientific and Technical Information (OSTI), January 2007. http://dx.doi.org/10.2172/926313.

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Worrell, W. L. Zirconia-based electrodes for solid oxide fuel cells. Office of Scientific and Technical Information (OSTI), December 1989. http://dx.doi.org/10.2172/7022625.

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Gorte, Raymond J., and John M. Vohs. The Development of Nano-Composite Electrodes for Solid Oxide Electrolyzers. Office of Scientific and Technical Information (OSTI), March 2014. http://dx.doi.org/10.2172/1124583.

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Ritter, James A. Supercapacitors and Batteries from Sol-Gel Derived Carbon - Metal Oxide Electrodes. Fort Belvoir, VA: Defense Technical Information Center, February 2001. http://dx.doi.org/10.21236/ada392659.

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Gopalan, Srikanth, and Ben Levitas. Core-Shell Heterostructures as Functional Materials for Solid Oxide Fuel Cell (SOFC) Electrodes. Office of Scientific and Technical Information (OSTI), June 2022. http://dx.doi.org/10.2172/1872369.

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Prof. Anil V. Virkar. LOW-TEMPERATURE, ANODE-SUPPORTED HIGH POWER DENSITY SOLID OXIDE FUEL CELLS WITH NANOSTRUCTURED ELECTRODES. Office of Scientific and Technical Information (OSTI), April 2000. http://dx.doi.org/10.2172/784599.

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Virkar, Anil V. LOW-TEMPERATURE, ANODE-SUPPORTED HIGH POWER DENSITY SOLID OXIDE FUEL CELLS WITH NANOSTRUCTURED ELECTRODES. Office of Scientific and Technical Information (OSTI), April 2000. http://dx.doi.org/10.2172/788101.

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Anil V. Virkar. LOW-TEMPERATURE, ANODE-SUPPORTED HIGH POWER DENSITY SOLID OXIDE FUEL CELLS WITH NANOSTRUCTURED ELECTRODES. Office of Scientific and Technical Information (OSTI), September 2001. http://dx.doi.org/10.2172/833838.

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Anil V. Virkar. LOW-TEMPERATURE, ANODE-SUPPORTED HIGH POWER DENSITY SOLID OXIDE FUEL CELLS WITH NANOSTRUCTURED ELECTRODES. Office of Scientific and Technical Information (OSTI), March 2002. http://dx.doi.org/10.2172/833840.

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Anil V. Virkar. LOW-TEMPERATURE, ANODE-SUPPORTED HIGH POWER DENSITY SOLID OXIDE FUEL CELLS WITH NANOSTRUCTURED ELECTRODES. Office of Scientific and Technical Information (OSTI), June 2001. http://dx.doi.org/10.2172/833876.

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