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Sample records for anodic oxide films

  1. Formation and Morphology of Anodic Oxide Films of Ti

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    The morphology and structure of the oxide films of Ti in H3PO4 were investigated by galvanostatic anodization, SEM and XRD. The oxide film grew from some pores in the grooves to layered microdomains as increasing anodizing voltage. The crystallinity of the oxide films decreased with the increase of the concentration of the electrolyte. The model has been proposed for the growth of the oxide films by two steps, i.e. by uniform thickening and by local deposition.

  2. Tunable structural color of anodic tantalum oxide films

    Institute of Scientific and Technical Information of China (English)

    Sheng Cui-Cui; Cai Yun-Yu; Dai En-Mei; Liang Chang-Hao

    2012-01-01

    Tantalum (Ta) oxide films with tunable structural color were fabricated easily using anodic oxidation.The structure,components,and surface valence states of the oxide filns were investigated by using gazing incidence X-ray diffractometry,X-ray photoelectron microscopy,and surface analytical techniques.Their thickness and optical properties were studied by using spectroscopic ellipsometry and total reflectance spectrum.Color was accurately defined using L*a*b* scale.The thickness of compact Ta2O5 films was linearly dependent on anodizing voltage.The film color was tunable by adjusting the anodic voltage.The difference in color appearance resulted from the interference behavior between the interfaces of air-oxide and oxide-metal.

  3. Synthesis of iridescent Ni-containing anodic aluminum oxide films by anodization in oxalic acid

    Science.gov (United States)

    Xu, Qin; Ma, Hong-Mei; Zhang, Yan-Jun; Li, Ru-Song; Sun, Hui-Yuan

    2016-02-01

    Ni-containing anodic aluminum oxide films with highly saturated colors were synthesized using an ac electrodeposition method, and the optical and magnetic characteristics of the films were characterized. Precisely controllable color tuning could be obtained using wet-chemical etching to thin and widen the anodic aluminum oxide films pores isotropically before Ni deposition. Magnetic measurements indicate that such colored composite films not exhibit obvious easy magnetization direction. The resulted short (200 nm in length) and wide (50 nm in diameter) Ni nanowires present only fcc phase. The magnetization reversal mechanism is in good agreement with the symmetric fanning reversal mode which is discussed in detail. Such films may find applications in decoration, display and multifunctional anti-counterfeiting applications.

  4. Structural transformation of nickel hydroxide films during anodic oxidation

    Energy Technology Data Exchange (ETDEWEB)

    Crocker, R.W.; Muller, R.H.

    1992-05-01

    The transformation of anodically formed nickel hydroxide/oxy-hydroxide electrodes has been investigated. A mechanism is proposed for the anodic oxidation reaction, in which the reaction interface between the reduced and oxidized phases of the electrode evolves in a nodular topography that leads to inefficient utilization of the active electrode material. In the proposed nodular transformation model for the anodic oxidation reaction, nickel hydroxide is oxidized to nickel oxy-hydroxide in the region near the metal substrate. Since the nickel oxy-hydroxide is considerably more conductive than the surrounding nickel hydroxide, as further oxidation occurs, nodular features grow rapidly to the film/electrolyte interface. Upon emerging at the electrolyte interface, the reaction boundary between the nickel hydroxide and oxy-hydroxide phases spreads laterally across the film/electrolyte interface, creating an overlayer of nickel oxy-hydroxide and trapping uncharged regions of nickel hydroxide within the film. The nickel oxy-hydroxide overlayer surface facilitates the oxygen evolution side reaction. Scanning tunneling microscopy of the electrode in its charged state revealed evidence of 80 {endash} 100 Angstrom nickel oxy-hydroxide nodules in the nickel hydroxide film. In situ spectroscopic ellipsometer measurements of films held at various constant potentials agree quantitatively with optical models appropriate to the nodular growth and subsequent overgrowth of the nickel oxy-hydroxide phase. A two-dimensional, numerical finite difference model was developed to simulate the current distribution along the phase boundary between the charged and uncharged material. The model was used to explore the effects of the physical parameters that govern the electrode behavior. The ratio of the conductivities of the nickel hydroxide and oxy-hydroxide phases was found to be the dominant parameter in the system.

  5. Submicron fabrication by local anodic oxidation of germanium thin films

    Science.gov (United States)

    Oliveira, A. B.; Medeiros-Ribeiro, G.; Azevedo, A.

    2009-08-01

    Here we describe a lithography scheme based on the local anodic oxidation of germanium film by a scanning atomic force microscope in a humidity-controlled atmosphere. The oxidation kinetics of the Ge film were investigated by a tapping mode, in which a pulsed bias voltage was synchronized and applied with the resonance frequency of the cantilever, and by a contact mode, in which a continuous voltage was applied. In the tapping mode we clearly identified two regimes of oxidation as a function of the applied voltage: the trench width increased linearly during the vertical growth and increased exponentially during the lateral growth. Both regimes of growth were interpreted taking into consideration the Cabrera-Mott mechanism of oxidation applied to the oxide/Ge interface. We also show the feasibility of the bottom-up fabrication process presented in this work by showing a Cu nanowire fabricated on top of a silicon substrate.

  6. Properties of thin anodic oxide films on zirconium alloys

    International Nuclear Information System (INIS)

    Thin (0.1-0.2 μm) anodic oxide films were formed on zirconium, Zircaloy-2 and Zr-2.5 wt% Nb alloy specimens and examined by AC impedance spectroscopy (using both metal and aqueous electrolyte contacts), UV/VIS interferometry, and scanning electron microscopy (SEM). The SEM studies showed that the extent of oxide cracking was a function of the particular alloy and the electrolyte in which the oxide was formed. AC impedance spectroscopy showed that with metallic contacts a Young impedance behaviour was observed as a result of local conduction paths in the oxide film, probably resulting from second phase particles. The extent of cracking in the oxide was identified best from SEM and AC impedance measurements in aqueous electrolytes, and did not appear to contribute to the results obtained with metallic contacts. Large discrepancies between the apparent oxide thicknesses measured from AC impedance data obtained from measurements with aqueous electrolyte and liquid metal contacts, respectively, were shown to result from surface roughness and inadequate wetting by the liquid metals. These discrepancies could be eliminated by using evaporated platinum contacts, which also showed evidence for local conduction in the oxides. UV/VIS interferometry results for the oxide refractive indices and oxide thicknesses gave much scatter because of the small number of fringes available for the analysis and the difficulties in establishing the positions of interference minima with the same accuracy as was possible for interference maxima. The use of this combination of techniques still appears to be the best method for investigating the presence of conducting paths in thick porous oxide films on these alloys. Preference should be given to using evaporated rather than liquid metal contacts when studying such oxides. The advantages of easy removal for the liquid metal contacts often, however, outweigh the errors introduced by surface roughness when using them for repetitive measurements

  7. Formation of Porous Anodic Oxide Film on Titanium in Phosphoric Acid Electrolyte

    Science.gov (United States)

    Liu, Z.; Thompson, G. E.

    2015-01-01

    A sequential breakdown anodizing conditions on cp-Ti in phosphoric acid has been investigated in the present study. Anodic oxide films were formed at 100, 150, and 200 V, examined by scanning electron microscopy, Raman spectroscopy, glow discharge optical emission spectrometry, and electrochemical impedance spectroscopy. A porous oxide texture was formed at each voltage. The thickness of anodic porous oxide increased with the increase of anodic voltage. Nano-particulates were formed around and within the pores, and the size of pores increased with increased voltage due to the expansion of particulates. The amorphous-to-crystalline transition was initiated during the film growth. The degree of crystallinity in the anodic oxide film fabricated at 200 V is more abundant than 150 and 100 V. Increased content of the phosphorus species was incorporated into the porous film with the increase of anodic voltage, stabilizing for the nanocrystals developed within the oxide.

  8. Anodic luminescence, structural, photoluminescent, and photocatalytic properties of anodic oxide films grown on niobium in phosphoric acid

    Science.gov (United States)

    Stojadinović, Stevan; Tadić, Nenad; Radić, Nenad; Stefanov, Plamen; Grbić, Boško; Vasilić, Rastko

    2015-11-01

    This article reports on properties of oxide films obtained by anodization of niobium in phosphoric acid before and after the dielectric breakdown. Weak anodic luminescence of barrier oxide films formed during the anodization of niobium is correlated to the existence of morphological defects in the oxide layer. Small sized sparks generated by dielectric breakdown of formed oxide film cause rapid increase of luminescence intensity. The luminescence spectrum of obtained films on niobium under spark discharging is composed of continuum radiation and spectral lines caused by electronic spark discharging transitions in oxygen and hydrogen atoms. Oxide films formed before the breakdown are amorphous, while after the breakdown oxide films are partly crystalline and mainly composed of Nb2O5 hexagonal phase. The photocatalytic activity of obtained oxide films after the breakdown was investigated by monitoring the degradation of methyl orange. Increase of the photocatalytic activity with time is related to an increase of oxygen vacancy defects in oxide films formed during the process. Also, higher concentration of oxygen vacancy defects in oxide films results in higher photoluminescence intensity.

  9. Luminescence properties of oxide films formed by anodization of aluminum in 12-tungstophosphoric acid

    International Nuclear Information System (INIS)

    In this paper, we have investigated luminescence properties of oxide films formed by anodization of aluminum in 12-tungstophosphoric acid. For the first time we have measured weak luminescence during anodization of aluminum in this electrolyte (so-called galvanoluminescence GL) and showed that there are wide GL bands in the visible region of the spectrum and observed two dominant spectral peaks. The first one is at about 425 nm, and the second one shifts with anodization voltage. As the anodization voltage approaches the breakdown voltage, a large number of sparks appear superimposed on the anodic GL. Several intensive band peaks were observed under breakdown caused by electron transitions in W, P, Al, O, H atoms. Furthermore, photoluminescence (PL) of anodic oxide films and anodic-spark formed oxide coatings were performed. In both cases wide PL bands in the range from 320 nm to 600 nm were observed.

  10. Photocatalytic activity of porous TiO2 films prepared by anodic oxidation

    Institute of Scientific and Technical Information of China (English)

    WANG Wei; TAO Jie; WANG Tao; WANG Ling

    2007-01-01

    Anatase titanium dioxide is an active photocatalyst, however, it is difficult to be immobilized on the substrate.The crystalline TiO2 porous film was prepared directly on the surface of pure titanium by anodic oxidation. The film was then used for photocatalysis via the methyl orange degradation method. The effects of anodization voltage, pH value, TiO2 film area and degradation time on the photocatalyst were investigated respectively by UV-visible spectrum. It was indicated that the TiO2 film prepared by anodic oxidation at 140 V had the best photocatalysis capability and the degradation of methyl orange was accelerated with acid addition.

  11. Electrophoretic deposition of PTFE particles on porous anodic aluminum oxide film and its tribological properties

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Dongya; Dong, Guangneng, E-mail: donggn@mail.xjtu.edu.cn; Chen, Yinjuan; Zeng, Qunfeng

    2014-01-30

    Polytetrafluoroethylene (PTFE) composite film was successfully fabricated by depositing PTFE particles into porous anodic aluminum oxide film using electrophoretic deposition (EPD) process. Firstly, porous anodic aluminum oxide film was synthesized by anodic oxidation process in sulphuric acid electrolyte. Then, PTFE particles in suspension were directionally deposited into the porous substrate. Finally, a heat treatment at 300 °C for 1 h was utilized to enhance PTFE particles adhesion to the substrate. The influence of anodic oxidation parameters on the morphology and micro-hardness of the porous anodic aluminum oxide film was studied and the PTFE particles deposited into the pores were authenticated using energy-dispersive spectrometer (EDS) and scanning electron microscopy (SEM). Tribological properties of the PTFE composite film were investigated under dry sliding. The experimental results showed that the composite film exhibit remarkable low friction. The composite film had friction coefficient of 0.20 which deposited in 15% PTFE emulsion at temperature of 15 °C and current density of 3 A/dm{sup 2} for 35 min. In addition, a control specimen of porous anodic aluminum oxide film and the PTFE composite film were carried out under the same test condition, friction coefficient of the PTFE composite film was reduced by 60% comparing with the control specimen at 380 MPa and 100 mm/s. The lubricating mechanism was that PTFE particles embedded in porous anodic aluminum oxide film smeared a transfer film on the sliding path and the micro-pores could support the supplement of solid lubricant during the sliding, which prolonged the lubrication life of the aluminum alloys.

  12. Electrophoretic deposition of PTFE particles on porous anodic aluminum oxide film and its tribological properties

    Science.gov (United States)

    Zhang, Dongya; Dong, Guangneng; Chen, Yinjuan; Zeng, Qunfeng

    2014-01-01

    Polytetrafluoroethylene (PTFE) composite film was successfully fabricated by depositing PTFE particles into porous anodic aluminum oxide film using electrophoretic deposition (EPD) process. Firstly, porous anodic aluminum oxide film was synthesized by anodic oxidation process in sulphuric acid electrolyte. Then, PTFE particles in suspension were directionally deposited into the porous substrate. Finally, a heat treatment at 300 °C for 1 h was utilized to enhance PTFE particles adhesion to the substrate. The influence of anodic oxidation parameters on the morphology and micro-hardness of the porous anodic aluminum oxide film was studied and the PTFE particles deposited into the pores were authenticated using energy-dispersive spectrometer (EDS) and scanning electron microscopy (SEM). Tribological properties of the PTFE composite film were investigated under dry sliding. The experimental results showed that the composite film exhibit remarkable low friction. The composite film had friction coefficient of 0.20 which deposited in 15% PTFE emulsion at temperature of 15 °C and current density of 3 A/dm2 for 35 min. In addition, a control specimen of porous anodic aluminum oxide film and the PTFE composite film were carried out under the same test condition, friction coefficient of the PTFE composite film was reduced by 60% comparing with the control specimen at 380 MPa and 100 mm/s. The lubricating mechanism was that PTFE particles embedded in porous anodic aluminum oxide film smeared a transfer film on the sliding path and the micro-pores could support the supplement of solid lubricant during the sliding, which prolonged the lubrication life of the aluminum alloys.

  13. Thin film fuel cells with vanadium oxide anodes: Strain and stoichiometry effects

    International Nuclear Information System (INIS)

    Highlights: • Vanadium oxides of varying stoichiometry have been studied as anodes in thin film solid oxide fuel cells. • V2O3 and V2O5 anodes show superior performance. • Calculated thermal strain and phase stability provide insights into experimental observations. - ABSTRACT: Thin film solid oxide fuel cells incorporating vanadium oxide anodes having open circuit potential of 1 V with hydrogen fuel have been realized. The as-deposited anode stoichiometry was varied by choice of growth conditions of vanadium oxide and a striking correlation to fuel cell performance (open circuit potential and peak power density) is observed. Possible mechanisms leading to the experimental observations based on calculated thermodynamic phase stability under fuel cell operating environments, spectroscopic analysis of the anodes and strain-related arguments are presented

  14. Anodic oxidation

    CERN Document Server

    Ross, Sidney D; Rudd, Eric J; Blomquist, Alfred T; Wasserman, Harry H

    2013-01-01

    Anodic Oxidation covers the application of the concept, principles, and methods of electrochemistry to organic reactions. This book is composed of two parts encompassing 12 chapters that consider the mechanism of anodic oxidation. Part I surveys the theory and methods of electrochemistry as applied to organic reactions. These parts also present the mathematical equations to describe the kinetics of electrode reactions using both polarographic and steady-state conditions. Part II examines the anodic oxidation of organic substrates by the functional group initially attacked. This part particular

  15. Formation of Al-Si Composite Oxide Film by Hydrolysis Precipitation and Anodizing

    Institute of Scientific and Technical Information of China (English)

    Zhe-Sheng Feng; Ying-Jie Xia; Jia Ding; Jin-Ju Chen

    2007-01-01

    This paper presents a new technique in the high dielectric constant composite oxide film preparation.On the basis of nanocompsite high dielectric constant aluminum oxide film growth technology, a new idea of adulterating Si oxide species into the aluminum composite film was proposed. As a result, the specific capacitance and withstanding voltage of the composite oxide film formed at the anodizing voltage of 20V are enhanced, and the leakage current of the aluminum composite oxide film is reduced through incorporation of Si oxide species.

  16. Anodic Oxidation in Aluminum Electrode by Using Hydrated Amorphous Aluminum Oxide Film as Solid Electrolyte under High Electric Field.

    Science.gov (United States)

    Yao, Manwen; Chen, Jianwen; Su, Zhen; Peng, Yong; Zou, Pei; Yao, Xi

    2016-05-01

    Dense and nonporous amorphous aluminum oxide (AmAO) film was deposited onto platinized silicon substrate by sol-gel and spin coating technology. The evaporated aluminum film was deposited onto the AmAO film as top electrode. The hydrated AmAO film was utilized as a solid electrolyte for anodic oxidation of the aluminum electrode (Al) film under high electric field. The hydrated AmAO film was a high efficiency electrolyte, where a 45 nm thick Al film was anodized completely on a 210 nm thick hydrated AmAO film. The current-voltage (I-V) characteristics and breakdown phenomena of a dry and hydrated 210 nm thick AmAO film with a 150 nm thick Al electrode pad were studied in this work. Breakdown voltage of the dry and hydrated 210 nm thick AmAO film were 85 ± 3 V (405 ± 14 MV m(-1)) and 160 ± 5 V (762 ± 24 MV m(-1)), respectively. The breakdown voltage of the hydrated AmAO film increased about twice, owing to the self-healing behavior (anodic oxidation reaction). As an intuitive phenomenon of the self-healing behavior, priority anodic oxidation phenomena was observed in a 210 nm thick hydrated AmAO film with a 65 nm thick Al electrode pad. The results suggested that self-healing behavior (anodic oxidation reaction) was occurring nearby the defect regions of the films during I-V test. It was an effective electrical self-healing method, which would be able to extend to many other simple and complex oxide dielectrics and various composite structures.

  17. The surface treatment on oxide film of pure titanium Part 1. The effect of Anodic oxidation

    Institute of Scientific and Technical Information of China (English)

    Ge Wang; Xiangrong Cheng

    2006-01-01

    目的:研究阳极氧化对纯钛种植材料氧化膜的影响.方法:5片直径9 mm厚2 mm的纯钛在升压速度为7~8 v/min、电流密度≤10 mA/cm2的条件下分别进行阳极氧化处理,(A)10 v 10 min,(B)24 v 10 min,(C) 40 v 10 min,(D)24 v 40 min,(E) 24 v 2 h.用potentiostat仪检测以上样品在生理盐水和人造海水中的电化学行为.结果:以上样品的颜色呈:A蓝色,B淡黄色,C粉红色,D金黄色,E深黄色.随着电压的升高和作用时间的延长,2.55峰渐渐强化,2.34峰弱化.在生理盐水中,阳极氧化膜的开路电势稳定于0 mV,而自然氧化膜则很快从-50上升到-40 mV,极化电流比自然氧化膜的低100倍.在人造海水中,阳极氧化膜的开路电势稳定在-90 mV,自然氧化膜则从-480 mV快速上升到-310 mV,且活化电流明显高于阳极氧化膜.结论:阳极氧化膜的颜色可能和膜的厚度有关,而颜色对种植体上的修复体有影响,因此,金黄色被选为理想的颜色.2.55和2.34峰的变化规律尚无法解释.阳极氧化膜的稳定性和耐腐蚀性远远高于自然氧化膜.因此,阳极氧化法是一种提高纯钛氧化膜耐腐蚀性的好方法.%Objectives: To study the oxide film of pure titanium implant material treated by anodic oxidation. Methods: Five commercially pure (CP) titanium sheets (9mm in diameter and 2mm thick) were treated by the speed of 7-8 v/min of potential, the current density ≤10mA/cm2 to (A) 10v for 10min, (B) 24v for 10min, (C) 40v for 10min, (D) 24v for 40min, (E) 24v for 2hr in Kawahara's electrochemical solution. The electro-chemical behavior of anodic oxide film and natural oxide film was studied using a potentiostat. Results: The samples color changed from white to the following sequence blue, light gold, pink, media gold and dark gold. Along with potential and time going on, XRD patterns showed that the peak 2.55 strengthened, and peak 2.34 weakened. The voltage-time curve in physiological salt solution (PSS) showed

  18. Preparation and crystalline phase of a TiO2 porous film by anodic oxidation

    Institute of Scientific and Technical Information of China (English)

    WANG Wei; TAO Jie; ZHANG Weiwei; TAO Haijun; WANG Ling

    2005-01-01

    Anatase titanium dioxide is an active photocatalyst, but it is difficult to immobilize on the substrate. A crystalline TiO2 porous film was prepared directly on the surface of pure titanium by anodic oxidation in this work. Constant voltage and constant current anodic oxidation were adopted with sulphuric acid used as the electrolyte, pure titanium as the anode and copper as the cathode. The morphology and structure of the porous film on the substrate were analyzed with the aid of Field Emission Scanning Electron Microscopy (FESEM) and X-ray Diffraction (XRD). The effects of the parameters of anodic oxidation (such as voltage, the concentration of sulphuric acid, anodization time and current density) on the aperture and the crystalline phase of the TiO2 porous film were systematically investigated. The results indicate that the increase of current density facilitates the augment of the aperture and the generation of anatase and rutile. In addition, the forming mechanism of anatase and rutile TiO2 porous films was discussed.

  19. Modelling the growth process of porous aluminum oxide film during anodization

    Science.gov (United States)

    Aryslanova, E. M.; Alfimov, A. V.; Chivilikhin, S. A.

    2015-11-01

    Currently it has become important for the development of metamaterials and nanotechnology to obtain regular self-assembled structures. One such structure is porous anodic alumina film that consists of hexagonally packed cylindrical pores. In this work we consider the anodization process, our model takes into account the influence of layers of aluminum and electrolyte on the rate of growth of aluminum oxide, as well as the effect of surface diffusion. In present work we consider those effects. And as a result of our model we obtain the minimum distance between centers of alumina pores in the beginning of anodizing process.

  20. Electrochromic Properties of Iridium Oxide Films Prepared by Pulsed Anodic Electrodeposition

    Science.gov (United States)

    Jung, Youngwoo; Tak, Yongsug; Lee, Jaeyoung

    2002-12-01

    Thin films of iridium oxide to be used as an electrochromic material were prepared by pulsed anodic current electrodeposition onto indium tin oxide (ITO) coated glass substrates. Before the pulsed electrodeposition, iridium oxide films formed by cyclic voltammetry (CV) played an important role in good adhesion as a seed layer. Iridium oxide films with light-blue color (100 mC/cm2) were deposited when anodic current of 0.07 mA/cm2 for 0.5 sec was superimposed on off-time of 0.5 sec (i.e., zero current) in each cycle. During CV experiment in phosphate buffered saline solution, electrodeposited iridium oxide films exhibited anodic electrochromism of blue and black color at two oxidation potentials (i.e., the ejection of H+) of +0.5 V and +0.9 V (vs. SCE), respectively, while on the cathodic scan, black thin film became colorless due to the injection of H+. When +0.9 V and -0.7 V were applied for coloring and bleaching observation in different pulse voltammetry, minimal times needed for each process are 9 sec and 5 sec, respectively.

  1. Electromechanical Breakdown of Barrier-Type Anodized Aluminum Oxide Thin Films Under High Electric Field Conditions

    Science.gov (United States)

    Chen, Jianwen; Yao, Manwen; Yao, Xi

    2016-02-01

    Barrier-type anodized aluminum oxide (AAO) thin films were formed on a polished aluminum substrate via electrochemical anodization in 0.1 mol/L aqueous solution of ammonium pentaborate. Electromechanical breakdown occurred under high electric field conditions as a result of the accumulation of mechanical stress in the film-substrate system by subjecting it to rapid thermal treatment. Before the breakdown event, the electricity of the films was transported in a highly nonlinear way. Immediately after the breakdown event, dramatic cracking of the films occurred, and the cracks expanded quickly to form a mesh-like dendrite network. The breakdown strength was significantly reduced because of the electromechanical coupling effect, and was only 34% of the self-healing breakdown strength of the AAO film.

  2. Synthesis and properties of iridescent Zn-containing anodic aluminum oxide films

    Energy Technology Data Exchange (ETDEWEB)

    Jia, Xiaoxuan; Sun, Huiyuan, E-mail: huiyuansun@126.com; Liu, Lihu; Hou, Xue; Liu, Huiyuan

    2015-07-01

    A simple method of fabricating Zn-containing anodic aluminum oxide films for multifunctional anticounterfeit technology is reported. The resulting membranes were characterized with UV–vis illumination studies, natural light illumination color experiments, and electron microscopy analysis. Deposition of Zn in the nanopore region can enhance the color saturation of the thin alumina film with different colors dramatically. Both the anodization time and etching time have great influence on the structural color. The mechanisms for the emergence of this phenomenon are discussed and theoretical analysis further demonstrates the experimental results. - Highlights: • Iridescent PAA@Zn nanocomposite films were successfully fabricated. • A simple organics-assisted method is applied to making a series of fancy and multicolor patterns. • The color varies with the angle of incidence of the light used to view the film as is expected with Bragg–Snell formula. • Such colored films could be used in multifunctional anti-counterfeiting applications.

  3. Characterization of native and anodic oxide films formed on commercial pure titanium using electrochemical properties and morphology techniques

    International Nuclear Information System (INIS)

    Potentiostatically anodized oxide films on the surface of commercial pure titanium (cp-Ti) formed in sulfuric (0.5 M H2SO4) and in phosphoric (1.4 M H3PO4) acid solutions under variables anodizing voltages were investigated and compared with the native oxide film. Potentiodynamic polarization and electrochemical impedance spectroscopy, EIS, were used to predicate the different in corrosion behavior of the oxide film samples. Scanning electron microscope, SEM, and electron diffraction X-ray analysis, EDX, were used to investigate the difference in the morphology between different types of oxide films. The electrochemical characteristics were examined in phosphate saline buffer solution, PSB (pH 7.4) at 25 deg. C. Results have been shown that the nature of the native oxide film is thin and amorphous, while the process of anodization of Ti in both acid solutions plays an important role in changing the properties of passive oxide films. Significant increase in the corrosion resistance of the anodized surface film was recorded after 3 h of electrode immersion in PSB. On the other side, the coverage (θ) of film formed on cp-Ti was differed by changing the anodized acid solution. Impedance results showed that both the native film and anodized film formed on cp-Ti consist of two layers. The resistance of the anodized film has reached to the highest value by anodization of cp-Ti in H3PO4 and the inner layer in the anodized film formed in both acid solutions is also porous.

  4. Properties of anodic oxides grown on a hafnium–tantalum–titanium thin film library

    International Nuclear Information System (INIS)

    A ternary thin film combinatorial materials library of the valve metal system Hf–Ta–Ti obtained by co-sputtering was studied. The microstructural and crystallographic analysis of the obtained compositions revealed a crystalline and textured surface, with the exception of compositions with Ta concentration above 48 at.% which are amorphous and show a flat surface. Electrochemical anodization of the composition spread thin films was used for analysing the growth of the mixed surface oxides. Oxide formation factors, obtained from the potentiodynamic anodization curves, as well as the dielectric constants and electrical resistances, obtained from electrochemical impedance spectroscopy, were mapped along two dimensions of the library using a scanning droplet cell microscope. The semiconducting properties of the anodic oxides were mapped using Mott–Schottky analysis. The degree of oxide mixing was analysed qualitatively using x-ray photoelectron spectroscopy depth profiling. A quantitative analysis of the surface oxides was performed and correlated to the as-deposited metal thin film compositions. In the concurrent transport of the three metal cations during oxide growth a clear speed order of Ti > Hf > Ta was proven. (paper)

  5. Operational characteristics of thin film solid oxide fuel cells with ruthenium anode in natural gas

    Science.gov (United States)

    Takagi, Yuto; Kerman, Kian; Ko, Changhyun; Ramanathan, Shriram

    2013-12-01

    Direct utilization of hydrocarbons in low temperature solid oxide fuel cells is of growing interest in the landscape of alternative energy technologies. Here, we report on performance of self-supported micro-solid oxide fuel cells (μSOFCs) with ruthenium (Ru) nano-porous thin film anodes operating in natural gas and methane. The μSOFCs consist of 8 mol% yttria-stabilized zirconia thin film electrolytes, porous platinum cathodes and porous Ru anodes, and were tested with dry natural gas and methane as fuels and air as the oxidant. At 500 °C, comparable power densities of 410 mW cm-2 and 440 mW cm-2 were obtained with dry natural gas and methane, respectively. In weakly humidified natural gas, open circuit voltage of 0.95 V at 530 °C with peak power density of 800 mW cm-2 was realized. The μSOFC was continuously operated at constant voltage of 0.7 V with methane, where quasi-periodic oscillatory behavior of the performance was observed. Through post-operation XPS studies it was found that the oxidation state of Ru anode surfaces significantly differs depending on the fuel used, oxidation being enhanced with methane or natural gas. The nature of the oscillation is discussed based on the transition in surface oxygen coverage states and electro-catalytic activity of Ru anodes.

  6. Calcination/acid-activation treatment of an anodic oxidation TiO2/Ti film catalyst

    Institute of Scientific and Technical Information of China (English)

    YAO Zhongping; JIANG Yanli; JIANG Zhaohua; ZHU Hongkui; BAI Xuefeng

    2009-01-01

    The aim of this work was to investigate the effects of calcination/acid-activation on the composition, structure, and photocatalytic (PC) re-duction property of an anodic oxidation TiO2/Ti film catalyst. The surface morphology and phase composition were examined by scanning electron microscopy and X-ray diffraction. The catalytic property of the film catalysts was evaluated through the removal rate of potassium chromate during the PC reduction process. The results showed that the film catalysts were composed of anatase and mtile TiO2 with a mi-cro-porous surface structure. The calcination treatment increased the content of TiO2 in the film, changed the relative ratio of anatase and rutile TiO2, and decreased the size of the micro pores of the film cat.a/ysts. The removal rate of potassium chromate was related to the tech-nique parameters of calcination/acid-activation treatment. When the anodic oxidation TiO2Ti film catalyst was calcined at 873 K for 30 min and then acid-activated in the concentrated H2SO4 for 60 min, it presented the highest catalytic property, with the removal rate of potassium chromate of 96.3% during the PC reduction process under the experimental conditions.

  7. Synthesis of Coral-Like Tantalum Oxide Films via Anodization in Mixed Organic-Inorganic Electrolytes

    Science.gov (United States)

    Yu, Hongbin; Zhu, Suiyi; Yang, Xia; Wang, Xinhong; Sun, Hongwei; Huo, Mingxin

    2013-01-01

    We report a simple method to fabricate nano-porous tantalum oxide films via anodization with Ta foils as the anode at room temperature. A mixture of ethylene glycol, phosphoric acid, NH4F and H2O was used as the electrolyte where the nano-porous tantalum oxide could be synthesized by anodizing a tantalum foil for 1 h at 20 V in a two–electrode configuration. The as-prepared porous film exhibited a continuous, uniform and coral-like morphology. The diameters of pores ranged from 30 nm to 50 nm. The pores interlaced each other and the depth was about 150 nm. After calcination, the as-synthesized amorphous tantalum oxide could be crystallized to the orthorhombic crystal system. As observed in photocatalytic experiments, the coral-like tantalum oxide exhibited a higher photocatalytic activity for the degradation of phenol than that with a compact surface morphology, and the elimination rate of phenol increased by 66.7%. PMID:23799106

  8. Synthesis of coral-like tantalum oxide films via anodization in mixed organic-inorganic electrolytes.

    Directory of Open Access Journals (Sweden)

    Hongbin Yu

    Full Text Available We report a simple method to fabricate nano-porous tantalum oxide films via anodization with Ta foils as the anode at room temperature. A mixture of ethylene glycol, phosphoric acid, NH4F and H2O was used as the electrolyte where the nano-porous tantalum oxide could be synthesized by anodizing a tantalum foil for 1 h at 20 V in a two-electrode configuration. The as-prepared porous film exhibited a continuous, uniform and coral-like morphology. The diameters of pores ranged from 30 nm to 50 nm. The pores interlaced each other and the depth was about 150 nm. After calcination, the as-synthesized amorphous tantalum oxide could be crystallized to the orthorhombic crystal system. As observed in photocatalytic experiments, the coral-like tantalum oxide exhibited a higher photocatalytic activity for the degradation of phenol than that with a compact surface morphology, and the elimination rate of phenol increased by 66.7%.

  9. Indium-Doped Zinc Oxide Thin Films as Effective Anodes of Organic Photovoltaic Devices

    Directory of Open Access Journals (Sweden)

    Ziyang Hu

    2011-01-01

    Full Text Available Indium-doped zinc oxide (IZO thin films were prepared by low-cost ultrasonic spray pyrolysis (USP. Both a low resistivity (3.13×10−3 Ω cm and an average direct transmittance (400∼1500 nm about 80% of the IZO films were achieved. The IZO films were investigated as anodes in bulk-heterojunction organic photovoltaic (OPV devices based on poly(3-hexylthiophene and [6,6]-phenyl C61-butyric acid methyl ester. The device fabricated on IZO film-coated glass substrate showed an open circuit voltage of 0.56 V, a short circuit current of 8.49 mA cm-2, a fill factor of 0.40, and a power conversion efficiency of 1.91%, demonstrating that the IZO films prepared by USP technique are promising low In content and transparent electrode candidates of low-cost OPV devices.

  10. Effect of UV radiation on the growth and breakdown voltage of anodic oxide films on niobium

    International Nuclear Information System (INIS)

    Formation rates of anodic Nb2O5 films grown under galvanostatic conditions decrease in the presence of UV radiation, unlike those grown in the absence of UV radiation. This may be due to the development of a positive space charge near the solution/oxide interface which is responsible for an increase in electronic current in the film during its formation. Value of breakdown voltage also increases in the presence of UV radiations. The effect of current density and resistivity of the solution upon the breakdown voltage, both in the presence and absence of UV radiation, is discussed in terms of Ikonopisov theory of breakdown voltage. (author). 19 refs., 6 figs

  11. Effect of anodic oxide films on low temperature mechanical behavior of niobium single crystals

    International Nuclear Information System (INIS)

    The effect of thin (less than or equal to 1500 A) anodic oxide films on the mechanical behavior of single crystals of niobium at low temperatures (T less than or equal to 0.15 T/sub M/) was investigated. Oxide films affect mechanical behavior in two ways: the yield stress is reduced and the stress-strain curves are serrated over an appreciable range of strains. When oxide-coated specimens are also prestrained into stage I at 3000K, the serrations observed at low temperatures disappear, the flow stress is further reduced, the ductility is increased, and a three-stage work hardening behavior occurs. A model involving generation and motion of nonscrew dislocations from the oxide-metal interface is used to explain the results

  12. Corrosion Behavior of Anodic Oxidized TiO2 Film in Seawater

    Institute of Scientific and Technical Information of China (English)

    WANG Min; WANG Wei; HE Benlin; SUN Mingliang; YIN Yansheng; LIU Lan; ZOU Wuyuan; XU Xuefei

    2010-01-01

    TiO2 films were formed on metallic titanium substrates by the anodic oxidation method in H2SO4 solution under the 80V D.C..Phase component and microstructure were characterized by X-ray diffraction(XRD)and scanning electron microscopy(SEM).Water contact angles on titanium oxide film surface were measured under both dark and sunlight illumination conditions.Corrosion tests were carried out in seawater under different illumination conditions by electrochemistry impedance spectrum(EIS)and polarization curves.The result showed that the TiO2 film prepared by the anodic oxidation method was anatase with a uniform structure and without obvious pores or cracks on its surface.The average water contact angle of the film was 116.4 ° in dark,in contrast to an angle of 42.7 ° under the UV illumination for 2 hours,which demonstrates good hydrophobic property.The anti-corrosion behavior of the TiO2 film was declining with the extended immersion time.Under dark conditions,however,the hydrophobic TiO2 film retarded the water infiltrating into the substrate.The impedance changed slowly and the corrosion current density was 2 orders of magnitude lower than that with the film illuminated by sunlight.All of those mentioned above indicate that the TiO2 film possesses much better performance under dark condition,and it can be applied as an engineering material under dark seawater environment.

  13. Heterogeneous growth of anodic oxide film on a polycrystalline titanium electrode observed with a scanning electrochemical microscope

    Energy Technology Data Exchange (ETDEWEB)

    Fushimi, Koji; Okawa, Tsuyoshi; Azumi, Kazuhisa; Seo, Masahiro

    2000-02-01

    A scanning electrochemical microscope (SECM) was applied to study anodic oxide film grown on a polycrystalline titanium electrode in deaerated pH 8.4 borate solution. The probe current images of SECM could detect the heterogeneous growth of anodic oxide film, depending on the substrate crystal grains. This heterogeneity increased with increasing the film formation potential at the potential higher than 3 V (SHE). The study of the dependence of film thickness on the substrate grain has been also supported with Raman microprobe spectroscopy.

  14. Impact of nanostructured anode on low-temperature performance of thin-film-based anode-supported solid oxide fuel cells

    Science.gov (United States)

    Park, Jung Hoon; Han, Seung Min; Yoon, Kyung Joong; Kim, Hyoungchul; Hong, Jongsup; Kim, Byung-Kook; Lee, Jong-Ho; Son, Ji-Won

    2016-05-01

    The impact of a nanostructured Ni-yttria-stabilized zirconia (Ni-YSZ) anode on low-temperature solid oxide fuel cell (LT-SOFC) performance is investigated. By modifying processing techniques for the anode support, anode-supported SOFCs based on thin-film (∼1 μm) electrolytes (TF-SOFCs) with and without the nanostructured Ni-YSZ (grain size ∼100 nm) anode are fabricated and a direct comparison of the TF-SOFCs to reveal the role of the nanostructured anode at low temperature is made. The cell performance of the nanostructured Ni-YSZ anode significantly increases as compared to that of the cell without it, especially at low temperatures (500 °C). The electrochemical analyses confirm that increasing the triple-phase boundary (TPB) density near the electrolyte and anode interface by the particle-size reduction of the anode increases the number of sites available for charge transfer. Thus, the nanostructured anode not only secures the structural integrity of the thin-film components over it, it is also essential for lowering the operating temperature of the TF-SOFC. Although it is widely considered that the cathode is the main factor that determines the performance of LT-SOFCs, this study directly proves that anode performance also significantly affects the low-temperature performance.

  15. An anode with aluminum doped on zinc oxide thin films for organic light emitting devices

    International Nuclear Information System (INIS)

    Doped zinc oxides are attractive alternative materials as transparent conducting electrode because they are nontoxic and inexpensive compared with indium tin oxide (ITO). Transparent conducting aluminum-doped zinc oxide (AZO) thin films have been deposited on glass substrates by DC reactive magnetron sputtering method. Films were deposited at a substrate temperature of 150-bar oC in 0.03 Pa of oxygen pressure. The electrical and optical properties of the film with the Al-doping amount of 2 wt% in the target were investigated. For the 300-nm thick AZO film deposited using a ZnO target with an Al content of 2 wt%, the lowest electrical resistivity was 4x10-4Ωcm and the average transmission in the visible range 400-700 nm was more than 90%. The AZO film was used as an anode contact to fabricate organic light-emitting diodes. The device performance was measured and the current efficiency of 2.9 cd/A was measured at a current density of 100 mA/cm2

  16. Surface enhanced Raman scattering of biospecies on anodized aluminum oxide films

    Science.gov (United States)

    Zhang, C.; Smirnov, A. I.; Hahn, D.; Grebel, H.

    2007-06-01

    Traditionally, aluminum and anodized aluminum oxide films (AAO) are not the platforms of choice for surface-enhanced raman scattering (SERS) experiments despite of the aluminum's large negative permittivity value. Here we examine the usefulness of aluminum and nanoporous alumina platforms for detecting soft biospecies ranging from bacterial spores to protein markers. We used these flat platforms to examine SERS of a model protein (cytochrome c from bovine heart tissue) and bacterial cells (spores of Bacillus subtilis ATCC13933 used as Anthrax simulant) and demonstrated clear Raman amplification.

  17. Electrodeposited porous metal oxide films with interconnected nanoparticles applied as anode of lithium ion battery

    Energy Technology Data Exchange (ETDEWEB)

    Xiao, Anguo, E-mail: hixiaoanguo@126.com; Zhou, Shibiao; Zuo, Chenggang; Zhuan, Yongbing; Ding, Xiang

    2014-12-15

    Highlights: • Highly porous NiO film is prepared by a co-electrodeposition method. • Porous NiO film is composed of interconnected nanoparticles. • Porous structure is favorable for fast ion/electron transfer. • Porous NiO film shows good lithium ion storage properties. - Abstract: Controllable synthesis of porous metal oxide films is highly desirable for high-performance electrochemical devices. In this work, a highly porous NiO film composed of interconnected nanoparticles is prepared by a simple co-electrodeposition method. The nanoparticles in the NiO film have a size ranging from 30 to 100 nm and construct large-quantity pores of 20–120 nm. As an anode material for lithium ion batteries, the highly porous NiO film electrode delivers a high discharge capacity of 700 mA h g{sup −1} at 0.2 C, as well as good high-rate performance. After 100 cycles at 0.2 C, a specific capacitance of 517 mA h g{sup −1} is attained. The good electrochemical performance is attributed to the interconnected porous structure, which facilitates the diffusion of ion and electron, and provides large reaction surface area leading to improved performance.

  18. Ellipsometry of anodic film growth

    Energy Technology Data Exchange (ETDEWEB)

    Smith, C.G.

    1978-08-01

    An automated computer interpretation of ellisometer measurements of anodic film growth was developed. Continuous mass and charge balances were used to utilize more fully the time dependence of the ellipsometer data and the current and potential measurements. A multiple-film model was used to characterize the growth of films which proceeds via a dissolution--precipitation mechanism; the model also applies to film growth by adsorption and nucleation mechanisms. The characteristic parameters for film growth describe homogeneous and heterogeneous crystallization rates, film porosities and degree of hydration, and the supersaturation of ionic species in the electrolyte. Additional descriptions which may be chosen are patchwise film formation, nonstoichiometry of the anodic film, and statistical variations in the size and orientation of secondary crystals. Theories were developed to describe the optical effects of these processes. An automatic, self-compensating ellipsometer was used to study the growth in alkaline solution of anodic films on silver, cadmium, and zinc. Mass-transport conditions included stagnant electrolyte and forced convection in a flow channel. Multiple films were needed to characterize the optical properties of these films. Anodic films grew from an electrolyte supersatuated in the solution-phase dissolution product. The degree of supersaturation depended on transport conditions and had a major effect on the structure of the film. Anodic reaction rates were limited by the transport of charge carriers through a primary surface layer. The primary layers on silver, zinc, and cadmium all appeared to be nonstoichiometric, containing excess metal. Diffusion coefficients, transference numbers, and the free energy of adsorption of zinc oxide were derived from ellipsometer measurements. 97 figures, 13 tables, 198 references.

  19. Band gap structure modification of amorphous anodic Al oxide film by Ti-alloying

    DEFF Research Database (Denmark)

    Canulescu, Stela; Rechendorff, K.; Borca, C. N.;

    2014-01-01

    The band structure of pure and Ti-alloyed anodic aluminum oxide has been examined as a function of Ti concentration varying from 2 to 20 at. %. The band gap energy of Ti-alloyed anodic Al oxide decreases with increasing Ti concentration. X-ray absorption spectroscopy reveals that Ti atoms...... are not located in a TiO2 unit in the oxide layer, but rather in a mixed Ti-Al oxide layer. The optical band gap energy of the anodic oxide layers was determined by vacuum ultraviolet spectroscopy in the energy range from 4.1 to 9.2 eV (300–135 nm). The results indicate that amorphous anodic Al2O3 has a direct...

  20. Study on the influences of reduction temperature on nickel-yttria-stabilized zirconia solid oxide fuel cell anode using nickel oxide-film electrode

    Science.gov (United States)

    Jiao, Zhenjun; Ueno, Ai; Suzuki, Yuji; Shikazono, Naoki

    2016-10-01

    In this study, the reduction processes of nickel oxide at different temperatures were investigated using nickel-film anode to study the influences of reduction temperature on the initial performances and stability of nickel-yttria-stabilized zirconia anode. Compared to conventional nickel-yttria-stabilized zirconia composite cermet anode, nickel-film anode has the advantage of direct observation at nickel-yttria-stabilized zirconia interface. The microstructural changes were characterized by scanning electron microscopy. The reduction process of nickel oxide is considered to be determined by the competition between the mechanisms of volume reduction in nickel oxide-nickel reaction and nickel sintering. Electrochemical impedance spectroscopy was applied to analyze the time variation of the nickel-film anode electrochemical characteristics. The anode performances and microstructural changes before and after 100 hours discharging and open circuit operations were analyzed. The degradation of nickel-film anode is considered to be determined by the co-effect between the nickel sintering and the change of nickel-yttria-stabilized zirconia interface bonding condition.

  1. Formation of niobium oxide film with duplex layers by galvanostatic anodization

    International Nuclear Information System (INIS)

    Studies on niobium anodization in the mixture of 1 M H3PO4 and 1 wt % HF at galvanostatic anodization are described here in detail. Interestingly, duplex niobium oxide consisting of thick barrier oxide and correspondingly thick porous oxide was prepared at a constant current density of higher than 0.3 mAcm-2, whereas simple porous type oxide was formed at a current density of lower than 0.3 mAcm-2. In addition, simple barrier or porous type oxide was obtained by galvanostatic anodization at a single electrolyte of either 1 M H3PO4 or 1 wt % HF, respectively. The formation mechanism of duplex type structures was ascribed to different forming voltages required for moving anions

  2. Fabrication and characterization of anodic oxide films on a Ti-10V-2Fe-3Al titanium alloy

    Institute of Scientific and Technical Information of China (English)

    Jian-hua Liu; Jun-lan Yi; Song-mei Li; Mei Yu; Yong-zhen Xu

    2009-01-01

    Anodic oxide films of the titanium alloy Ti-10V-2Fe-3Al in ammonium tartrate electrolyte without hydrofluoric acid or fluoride were fabricated.The morphology,components,and microstructure of the films were characterized by scanning electron mi-croscopy (SEM),X-ray photoelectron spectroscopy (XPS),X-ray diffraction (XRD),and Raman spectroscopy.The results showed that the films were thick,uniform,and nontransparent.Such films exhibited sedimentary morphology,with a thickness of about 3 μm,and the pore diameters of the deposits ranged from several hundred nanometers to 1.5 μm.The films were mainly titanium dioxide.Some coke-like deposits,which may contain or be changed by OH,NH,C-C,C-O,and C=O groups,were doped in the firms.The films were mainly amorphous with a small amount of anatase and rutile phase.

  3. FIB-SEM investigation of trapped intermetallic particles in anodic oxide films on AA1050 aluminium

    DEFF Research Database (Denmark)

    Jariyaboon, Manthana; Møller, Per; Dunin-Borkowski, Rafal E.;

    2011-01-01

    using focused ion beam-scanning electron microscopy (FIB-SEM), SEM, and EDX. Findings - The intermetallic particles in the substrate material consisted of Fe or both Fe and Si with two different structures: irregular and round shaped. FIB-SEM cross-sectioned images revealed that the irregular....../Si ratio of the intermetallic particles decreased after anodizing. Originality/value - This paper shows that dual beam FIB-SEM seems to be an easy, less time consuming and useful method to characterize the cross-sectioned intermetallic particles incorporated in anodic film on aluminium....

  4. Improving the stability of nanostructured silicon thin film lithium-ion battery anodes through their controlled oxidation.

    Science.gov (United States)

    Abel, Paul R; Lin, Yong-Mao; Celio, Hugo; Heller, Adam; Mullins, C Buddie

    2012-03-27

    Silicon and partially oxidized silicon thin films with nanocolumnar morphology were synthesized by evaporative deposition at a glancing angle, and their performance as lithium-ion battery anodes was evaluated. The incorporated oxygen concentration was controlled by varying the partial pressure of water during the deposition and monitored by quartz crystal microbalance, X-ray photoelectron spectroscopy. In addition to bulk oxygen content, surface oxidation and annealing at low temperature affected the cycling stability and lithium-storage capacity of the films. By simultaneously optimizing all three, films of ~2200 mAh/g capacity were synthesized. Coin cells made with the optimized films were reversibly cycled for ~120 cycles with virtually no capacity fade. After 300 cycles, 80% of the initial reversible capacity was retained. PMID:22372404

  5. Influence of voltage waveform on anodic film of AZ91 Mg alloy via plasma electrolytic oxidation: Microstructural characteristics and electrochemical responses

    Energy Technology Data Exchange (ETDEWEB)

    Ko, Young Gun [School of Materials Science and Engineering, Yeungnam University, Gyeongsan 712-749 (Korea, Republic of); Lee, Eung Seok [Department of Metallurgy and Materials Engineering, Hanyang University, Ansan 426-791 (Korea, Republic of); Shin, Dong Hyuk, E-mail: dhshin@hanyang.ac.kr [Department of Metallurgy and Materials Engineering, Hanyang University, Ansan 426-791 (Korea, Republic of)

    2014-02-15

    Highlights: • The effect of voltage waveform on the anodic film structure is significant. • The anodic film by asymmetric-sine wave is denser than that by half-sine wave. • Asymmetric-sine wave results in excellent electrochemical properties. -- Abstract: The present study investigated how the voltage waveform influenced the microstructural characteristics and electrochemical responses of the anodic film on AZ91 Mg alloy coated by plasma electrolytic oxidation (PEO). PEO coatings of AZ91 Mg alloy were performed for 600 s in an alkaline silicate electrolyte with respect to the voltage waveform such as half-sine and asymmetric-sine waveforms. Microstructural observations on cross section of the anodic film utilizing scanning electron microscope revealed that the anodic film formed via asymmetric-sine wave was much denser in structure than that via half-sine counterpart since the occurrence of the cathodic breakdown between the anodic pulses could effectively suppress the formation of the micro-pores and discharge channels in the anodic films. Thereby, the hardness and corrosion properties of the anodic film formed by asymmetric-sine wave were found to be superior to those by half-sine wave. In addition, electrochemical responses were interpreted in relation to the equivalent circuit model consisting of resistor and capacitor elements within an electrical cell.

  6. Electrical behaviour, characteristics and properties of anodic aluminium oxide films coloured by nickel electrodeposition

    OpenAIRE

    Arurault, Laurent; Zamora, Gaël; Vilar, Virginie; Winterton, Peter; Bes, René

    2010-01-01

    Porous anodic films on 1050 aluminium substrate were coloured by AC electrodeposition of nickel. Several experiments were performed at different deposition voltages and nickel concentrations in the electrolyte in order to correlate the applied electrical power to the electrical behaviour, as well as the characteristics and properties of the coatings. The content of nickel inside the coatings reached 1.67 g/m2, depending on the experimental conditions. According to the applied AC voltage in...

  7. Electron microscopic studies of anodic oxide films on the AZ91HP alloy

    Directory of Open Access Journals (Sweden)

    D. Peixoto Barbosa

    2003-01-01

    Full Text Available A Mg-9wt.Al-1wt.%Zn-alloy was anodized up to 90 V with constant current/constant voltage in an electrolyte which contained the compounds of the HAE-process (KOH, Al(OH3, KF, Na3PO4 and KMnO4. Electron microscopic examinations revealed a highly porous and irregular film structure. The distribution of the elements in the film was measured with energy dispersive spectrometry on specimens prepared in cross section for the transmission electron microscope. The main characteristic found was a fluoride-enriched zone of about 100 nm thickness at the metal / film interface. Practically no manganese from the permanganate was detected in this fluoride-enriched zone.

  8. The potential and challenges of thin-film electrolyte and nanostructured electrode for yttria-stabilized zirconia-base anode-supported solid oxide fuel cells

    Science.gov (United States)

    Noh, Ho-Sung; Yoon, Kyung Joong; Kim, Byung-Kook; Je, Hae-June; Lee, Hae-Weon; Lee, Jong-Ho; Son, Ji-Won

    2014-02-01

    Thin-film electrolytes and nanostructured electrodes are essential components for lowering the operation temperature of solid oxide fuel cells (SOFCs); however, reliably implementing thin-film electrolytes and nano-structure electrodes over a realistic SOFC platform, such as a porous anode-support, has been extremely difficult. If these components can be created reliably and reproducibly on porous substrates as anode supports, a more precise assessment of their impact on realistic SOFCs would be possible. In this work, structurally sound thin-film and nano-structured SOFC components consisting of a nano-composite NiO-yttria-stabilized zirconia (YSZ) anode interlayer, a thin YSZ and gadolinia-doped ceria (GDC) bi-layer electrolyte, and a nano-structure lanthanum strontium cobaltite (LSC)-base cathode, are sequentially fabricated on a porous NiO-YSZ anode support using thin-film technology. Using an optimized cell testing setup makes possible a more exact investigation of the potential and challenges of thin-film electrolyte and nanostructured electrode-based anode-supported SOFCs. Peak power densities obtained at 500 °C surpass 500 mW cm-2, which is an unprecedented low-temperature performance for the YSZ-based anode-supported SOFC. It is found that this critical, low-temperature performance for the anode-supported SOFC depends more on the electrode performance than the resistance of the thin-film electrolyte during lower temperature operation.

  9. Plasmon-induced optical switching of electrical conductivity in porous anodic aluminum oxide films encapsulated with silver nanoparticle arrays.

    Science.gov (United States)

    Huang, Chen-Han; Lin, Hsing-Ying; Lau, Ben-Chao; Liu, Chih-Yi; Chui, Hsiang-Chen; Tzeng, Yonhua

    2010-12-20

    We report on plasmon induced optical switching of electrical conductivity in two-dimensional (2D) arrays of silver (Ag) nanoparticles encapsulated inside nanochannels of porous anodic aluminum oxide (AAO) films. The reversible switching of photoconductivity greatly enhanced by an array of closely spaced Ag nanoparticles which are isolated from each other and from the ambient by thin aluminum oxide barrier layers are attributed to the improved electron transport due to the localized surface plasmon resonance and coupling among Ag nanoparticles. The photoconductivity is proportional to the power, and strongly dependent on the wavelength of light illumination. With Ag nanoparticles being isolated from the ambient environments by a thin layer of aluminum oxide barrier layer of controlled thickness in nanometers to tens of nanometers, deterioration of silver nanoparticles caused by environments is minimized. The electrochemically fabricated nanostructured Ag/AAO is inexpensive and promising for applications to integrated plasmonic circuits and sensors. PMID:21197062

  10. Highly transparent and conductive double-layer oxide thin films as anodes for organic light-emitting diodes

    International Nuclear Information System (INIS)

    Double-layer transparent conducting oxide thin film structures containing In-doped CdO (CIO) and Sn-doped In2O3 (ITO) layers were grown on glass by metal-organic chemical vapor deposition and ion-assisted deposition (IAD), respectively, and used as anodes for polymer light-emitting diodes (PLEDs). These films have a very low overall In content of 16 at. %. For 180-nm-thick CIO/ITO films, the sheet resistance is 5.6 Ω/□, and the average optical transmittance is 87.1% in the 400-700 nm region. The overall figure of merit (Φ=T10/Rsheet) of the double-layer CIO/ITO films is significantly greater than that of single-layer CIO, IAD-ITO, and commercial ITO films. CIO/ITO-based PLEDs exhibit comparable or superior device performance versus ITO-based control devices. CIO/ITO materials have a much lower sheet resistance than ITO, rendering them promising low In content electrode materials for large-area optoelectronic devices

  11. Nanoporous anodic aluminum oxide as a promising material for the electrostatically-controlled thin film interference filter

    International Nuclear Information System (INIS)

    This study presents the approach to implement the electrostatically-controlled thin film optical filter by using a nanoporous anodic aluminum oxide (np-AAO) layer as the key suspended micro structure. The bi-stable optical filter operates in the visible spectral range. In this work, the presented bi-stable optical filter has averaged reflectivity of 60%, and the central wavelengths are 580 and 690 nm respectively for on and off states. The presented np-AAO layer offers the following merits for the thin film optical filter: (1) material properties of np-AAO film, such as refractive index, elastic modulus and dielectric constant, can be easily changed by a low temperature pore-widening process, (2) in-use stiction of the suspended np-AAO structure can be reduced by the small contact area of nanoporous textures, (3) driving (pull-in) voltage can be reduced due to a large dielectric constant (εAAO is 7.05) and small stiffness of np-AAO film and (4) dielectric charging can be reduced by the np-AAO material; thus the offset voltage is small. The study reports the design, fabrication and experimental results of the bi-stable optical filter to demonstrate the advantages of the presented device. The np-AAO material also has the potential for applications of other electrostatic drive micro devices. (paper)

  12. Morphology and performances of the anodic oxide films on Ti6Al4V alloy formed in alkaline-silicate electrolyte with aminopropyl silane addition under low potential

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Jiali; Wang, Jinwei, E-mail: wangjw@ustb.edu.cn; Yuan, Hongye

    2013-11-01

    Oxide films on Ti6Al4V alloy are prepared using sodium hydroxide–sodium silicate as the base electrolyte with addition of aminopropyl trimethoxysilane (APS) as additive by potentiostatic anodizing under 10 V. APS is incorporated into the films during anodizing and the surface morphology of the oxide films is changed from particle stacked to honeycomb-like porous surfaces as shown by scanning electron microscopy (SEM) with Energy Disperse Spectroscopy (EDX). The surface roughness and aminopropyl existence on the oxide films result in their differences in wettability as tested by the surface profile topography and contact angle measurements. The anti-abrasive ability of the anodic films is improved with the addition of APS due to its toughening effects and serving as lubricants in the ceramic oxide films as measured by ball-on-disk friction test. Also, potentiodynamic corrosion test proves that their anticorrosive ability in 3.5 wt.% NaCl is greatly improved as reflected by their much lower corrosion current (I{sub corr}) and higher corrosion potential (E{sub corr}) than those of the substrate.

  13. Self-sealing of unsealed aluminium anodic oxide films in very different atmospheres

    Directory of Open Access Journals (Sweden)

    González, J. A.

    2003-12-01

    Full Text Available It is widely believed that the corrosion resistance behaviour of bare aluminium in natural environments is superior to that of unsealed anodised aluminium. However, results obtained in the exposure of unsealed anodised aluminium specimens with three different film thicknesses, in 9 atmospheres of Ibero-America with salinity levels between 3.9 and 517 mg.m-2.d-1 chloride, clearly shows the reverse to be true. After a sufficient time, which is shorter the higher the precipitation rate and the environmental relative humidity, a self-sealing process takes place, leading to coatings that surpass the quality standards demanded in industrial practice. Anodic films, sealed and unsealed, are protective coatings whose quality improves with ageing in most natural environments.

    Está muy difundida la idea de que el comportamiento del aluminio es superior al del aluminio anodizado y sin sellar, desde el punto de vista de la resistencia a la corrosión, en los ambientes naturales. Sin embargo, los resultados obtenidos en la exposición de anodizados sin sellar, de tres espesores diferentes, a 9 atmósferas de Iberoamérica, con salinidades comprendidas entre 3,9 y 517 mg.m-2.d-1 de cloruros, muestran, sin lugar a dudas, lo contrario. Con tiempo suficiente, tanto más rápidamente cuanto mayor sean las precipitaciones y la humedad relativa ambiental, tiene lugar un proceso de autosellado que conduce a recubrimientos que superan las normas de calidad exigidas en la práctica industrial. Los anodizados, sellados y sin sellar, son recubrimientos protectores que mejoran su calidad, en la mayoría de los ambientes naturales, con el envejecimiento.

  14. Influence of Nanowire Diameter on Structural and Optical Properties of cu Nanowire Synthesized in Anodic Aluminium Oxide Film

    Science.gov (United States)

    Cetinel, A.; Özcelik, Z.

    2016-11-01

    Copper (Cu) nanowire arrays embedded in anodic aluminium oxide films (AAO) on aluminium substrate have been synthesized by alternating current electrochemical deposition. Two-step anodization process has been performed to get the through-hole AAO with ordered nanochannels in 0.3M oxalic acids at DC voltages 30, 40, 50 and 60V, respectively. Structural characterization of the Cu nanowires has been analyzed by scanning electron microscopy (SEM) and X-ray diffraction (or) X-ray diffractometer (XRD). Our SEM analysis has revealed that the diameters of vertically oriented Cu nanowires are 15, 25, 45 and 60nm and the length of Cu nanowires having high packing density is about 15μm. XRD measurement has indicated that polycrystalline Cu nanowires prefer growth orientation along the (111) direction. Optical measurements show that reflection of the Cu nanowires/AAO on aluminium reduces with decreasing diameter of the Cu nanowires. This effect can be associated with increased light scattering from metal nanoparticles near their localized plasmon resonance frequency depending on the size and shape of the nanoparticles.

  15. Electrostatic layer-by-layer a of platinum-loaded multiwall carbon nanotube multilayer: A tunable catalyst film for anodic methanol oxidation

    International Nuclear Information System (INIS)

    A simple layer-by-layer (LBL) electrostatic adsorption technique was developed for deposition of films composed of alternating layers of positively charged poly(diallyldimethylammonium chloride) (PDDA) and negatively charged multiwall carbon nanotubes bearing platinum nanoparticles (Pt-CNTs). PDDA/Pt-CNT film structure and morphology up to six layers were characterized by scanning electron microscopy and ultraviolet-visible spectroscopy, showing the Pt-CNT layers to be porous and uniformly deposited within the multilayer films. Electrochemical properties of the PDDA/Pt-CNT films, as well as electrocatalytic activity toward methanol oxidation, were investigated with cyclic voltammetry. Significant activity toward anodic methanol oxidation was observed and is readily tunable through changing film thickness and/or platinum-nanoparticle loading. Overall, the observed properties of these PDDA/Pt-CNT multilayer films indicated unique potential for application in direct methanol fuel cell

  16. Facile fabrication of cuprous oxide nanocomposite anode films for flexible Li-ion batteries via thermal oxidation

    International Nuclear Information System (INIS)

    Graphical abstract: - Abstract: In the present work, nanostructured Cu2O films are directly grown from a Cu metal foil by means of a rapid thermal oxidation process. The structural characteristics of the films are investigated by field emission scanning electron microscopy, X-ray diffraction and attenuated total reflectance Fourier-transformed infrared spectroscopy. The electrochemical behaviour is investigated in both lithium (liquid electrolyte) and all-solid lithium polymer cells. At a discharge/charge rate of C/5, the films can provide a specific capacity greater than 220 mAh g−1 in the all-solid configuration, with excellent cycling stability and capacity retention after prolonged cycling. High surface area, short diffusion path and good conduction of the Cu2O films are considered to be responsible for the good electrochemical performance, along with the use of the polymeric electrolyte which is directly formed in situ on the electrode film surface. The present findings can provide a new and easy approach to fabricate nanocomposite films with interesting performance as negative electrode particularly for the next generation of flexible all-solid-state Li-ion microbatteries.

  17. Formation of complex anodic films on porous alumina matrices

    Indian Academy of Sciences (India)

    Alexander Zahariev; Assen Girginov

    2003-04-01

    The kinetics of growth of complex anodic alumina films was investigated. These films were formed by filling porous oxide films (matrices) having deep pores. The porous films (matrices) were obtained voltastatically in (COOH)2 aqueous solution under various voltages. The filling was done by re-anodization in an electrolyte solution not dissolving the film. Data about the kinetics of re-anodization depending on the porosity of the matrices were obtained. On the other hand, the slopes of the kinetic curves during reanodization were calculated by two equations expressing the dependence of these slopes on the ionic current density. A discrepancy was ascertained between the values of the calculated slopes and those experimentally found. For this discrepancy a possible explanation is proposed, related to the temperature increase in the film, because of that the real current density significantly increases during re-anodization.

  18. Self-assembly silicon/porous reduced graphene oxide composite film as a binder-free and flexible anode for lithium-ion batteries

    International Nuclear Information System (INIS)

    A Si/porous reduced graphene oxide (rGO) composite film synthesized by evaporation and leavening method are developed as a high-performance anode material for lithium ion batteries. The porous structure as buffer base can effectively release the volume expansion of the silicon particles, increase the electrical conductivity and reduce the transfer resistance of Li ions. The Si/porous rGO composite film presents high specific capacity and good cycling stability (1261 mA h g−1 at 50 mA g−1 up to 70 cycles), as well as enhanced rate capability. This approach to prepare such a unique structure is a low-cost and facile route for the silicon-based anode materials

  19. The passive film characterization and anodic polarization behavior of 11% Cr ferritic/martensitic and 15% Cr oxide dispersion strengthened steels in different electrolytic solutions

    International Nuclear Information System (INIS)

    The ferritic/martensitic (F/M) and oxide dispersion strengthened (ODS) steels are the most promising candidate materials for future nuclear power plants. In the present work, the passive film compositions and its correlation with anodic polarization behavior of 11% Cr F/M and 15% Cr ODS steels was examined in different electrolytic solutions of borate buffer, acidic, acidified chloride and in chloride solution. The X-ray photoelectron spectroscopy analysis of the passive film reveals the existence of the layers of Cr2O3 and Fe2O3 and in 15% Cr ODS steel along with Y2O3. The open circuit potential and potentiodynamic anodic polarization measurements show that pitting corrosion resistance is strongly dependent on electrolytic solutions and passive film compositions. The ODS steel indicated increased breakdown potential and wider passive range as compared to F/M steel in chloride containing media. In a non-chloride environment, this difference is not prominent. However, low pitting corrosion resistance of both steels in chloride solutions was attributable to Cl− and microstructural inhomogeneity. The SEM micrographs of surface morphology of corrosion attack showed severe pitting corrosion attack in chloride solutions. The anodic polarization behavior of F/M and ODS steels in different electrolytic solutions was studied for this work in relation to passive film compositions.

  20. 阳极氧化法制备多孔氧化铝膜的形成过程研究%Investigation on the growth sequence of porous anodic aluminum oxide films by two-step anodization

    Institute of Scientific and Technical Information of China (English)

    刘海凤; 路丙强; 梁冬林; 魏水强; 苟凯佩; 王凡; 文衍宣

    2012-01-01

    采用阳极氧化技术,研究了电压对多孔氧化铝膜生长过程的影响.使用扫描电镜( SEM)对在草酸-水-乙醇体系中形成的多孔氧化铝膜形貌进行观测.结果表明,在第二步氧化过程中,在40V氧化电压下,多孔氧化铝膜的有序度和孔径随反应时间延长而降低;在80 V下,经过长时间反应,AAO膜表面腐蚀严重,难以获得平整的多孔结构.预氧化过程所形成的薄氧化层有效保护了多孔氧化铝表面,同时对多孔结构具有短距离诱导作用.改变氧化电压、电解质浓度和反应时间,有序孔排列的结构参数也有所改变.高电场下,孔道的相互作用促进了其生长分化,形成了两种不同的孔道结构.%The detailed growth processes of porous anodic aluminum oxide films influenced by the applied voltage were studied via anodization method. The appearance of the porous anodic aluminum oxide films formed in oxalic acid-water-ethanol solution was studied by SEM. At the second anodization step, the ordering degree and pore size of oxide films decreased at 40 V, while the rough surface of AAO by severe corrosion was obtained at 80 V. Whereas, the surface oxide layer generated by pre-anodization provided effective protection at the early stage of high-voltage anodization, and guided the formation of ordered pores array in short range. The structural parameters of ordered pores array were dependent on the applied voltage, electrolyte concentration and reaction time. At high applied voltage, the cause of interaction forces between neighboring pores enhances the differentiation of pore growth, and hence two different pores growth behaviors in the internal and surface of AAO membrane are observed.

  1. Porous and mesh alumina formed by anodization of high purity aluminum films at low anodizing voltage

    Energy Technology Data Exchange (ETDEWEB)

    Abd-Elnaiem, Alaa M., E-mail: alaa.abd-elnaiem@science.au.edu.eg [KACST-Intel Consortium Center of Excellence in Nano-manufacturing Applications (CENA), Riyadh (Saudi Arabia); Physics Department, Faculty of Science, Assiut University, Assiut 71516 (Egypt); Mebed, A.M. [Physics Department, Faculty of Science, Assiut University, Assiut 71516 (Egypt); Department of Physics, Faculty of Science, Al-Jouf University, Sakaka 2014 (Saudi Arabia); El-Said, Waleed Ahmed [Department of Chemistry, Faculty of Science, Assiut University, Assiut 71516 (Egypt); Abdel-Rahim, M.A. [Physics Department, Faculty of Science, Assiut University, Assiut 71516 (Egypt)

    2014-11-03

    Electrochemical oxidation of high-purity aluminum (Al) films under low anodizing voltages (1–10) V has been conducted to obtain anodic aluminum oxide (AAO) with ultra-small pore size and inter-pore distance. Different structures of AAO have been obtained e.g. nanoporous and mesh structures. Highly regular pore arrays with small pore size and inter-pore distance have been formed in oxalic or sulfuric acids at different temperatures (22–50 °C). It is found that the pore diameter, inter-pore distance and the barrier layer thickness are independent of the anodizing parameters, which is very different from the rules of general AAO fabrication. The brand formation mechanism has been revealed by the scanning electron microscope study. Regular nanopores are formed under 10 V at the beginning of the anodization and then serve as a template layer dominating the formation of ultra-small nanopores. Anodization that is performed at voltages less than 5 V leads to mesh structured alumina. In addition, we have introduced a simple one-pot synthesis method to develop thin walls of oxide containing lithium (Li) ions that could be used for battery application based on anodization of Al films in a supersaturated mixture of lithium phosphate and phosphoric acid as matrix for Li-composite electrolyte. - Highlights: • We develop anodic aluminum oxide (AAO) with small pore size and inter-pore distance. • Applying low anodizing voltages onto aluminum film leads to form mesh structures. • The value of anodizing voltage (1–10 V) has no effect on pore size or inter-pore distance. • Applying anodizing voltage less than 5 V leads to mesh structured AAO. • AAO can be used as a matrix for Li-composite electrolytes.

  2. Corrosion Behaviour of Titanium Anodized Film in Different Corrosive Environments

    Directory of Open Access Journals (Sweden)

    Mr. Sunil D. Kahar

    2014-07-01

    Full Text Available Anodizing is an electrochemical process in which thickness of the natural oxide layer is increased and converted it into a decorative, durable, corrosion-resistant film. Titanium is used as a biocompatible material in human implants due to its excellent corrosion and wears resistance. Stable, continuous, highly adherent, and protective oxide films can be developed on titanium using various acid or alkaline baths. Anodizing of titanium generates a spectrum of different color without use of dyes. This spectrum of color dependent on the thickness of the oxide, voltage ranges, interference of light reflecting off the oxide surface and reflecting off the underlying metal surface. The anodized film of Titanium is mainly consists of TiO2 or mixtures of TiO2 & Ti2O3 etc. In the present work, Pure Titanium plate has been anodized using bath of Chromic Acid at different voltage range. The anodized film is characterized by visual observation, SEM & EDAX analysis & A.C Impedance Spectroscopy, while the corrosion studies were performed using Potentiodynamic studies were performed in 3.5% NaCl & 0.1N H2SO4. The Results show that the anodized film of Titanium show different spectrum of colors from Brown-Violet-Tea or Peacock. SEM & EDAX analyses show that the anodized film of Titanium is mainly made up of TiO2 and Ti2O3. Potentiodynamic study implies that the film developed on Titanium using the bath of Chromic Acid exhibits good corrosion resistance. The A.C. Impedance study shows that the film is more compact, adherent and more uniform in chromic acid bath.

  3. Enhancing low-field magnetoresistance of La0.67Ca0.33MnO3 films deposited on anodized aluminium-oxide membranes

    Institute of Scientific and Technical Information of China (English)

    Tang Wei-Hua; Li Pei-Gang; Lei Ming; Guo Yan-Feng; Chen Lei-Ming; Li Ling-Hong; Song Peng-Yun; Chen ChinPing

    2006-01-01

    In this paper we report a new method to fabricate nanostructured films.La0.67Ca0.33MnO3(LCMO)nanostructured films have been fabricated by using pulsed electron beam deposition (PED) on anodized aluminium oxide (AAO)membranes.The magnetic and electronic transport properties are investigated by using the Quantum Design physics properties measurement system (PPMS) and magnetic properties measurement system (MPMS).The resistance peak temperature (Tp) is about 85 K and the Curie temperature(Tc) is about 250 K for the LCMO film on an AAO membrane with a pore diameter of 20 nm.Large magnetoresistance ratio (MR) is observed near Tp.The MR is as high as 85 %under 1T magnetic field.The great enhancement of MR at low magnetic fields could be attributed to the lattice distortion and the grain boundary that are induced by the nanopores on the AAO membrane.

  4. Ultraviolet photoluminescence of porous anodic alumina films

    Institute of Scientific and Technical Information of China (English)

    2003-01-01

    Photoluminescence (PL) properties of porous anodic alumina (PAA) films prepared by using electrochemical anodization technique in a mixed solution of oxalic and sulfuric acid have been investigated. The PAA films have an intensive ultraviolet PL emission around 350 nm, of which a possible PL mechanism has been proposed. It was found that the incorporated oxalic ions, which could transform into PL centers and exist in the PAA films, are responsible for this ultraviolet PL emission.

  5. Improving the direct electron transfer in monolithic bioelectrodes prepared by immobilization of FDH enzyme on carbon-coated anodic aluminum oxide films

    Directory of Open Access Journals (Sweden)

    Alberto eCastro-Muñiz

    2016-02-01

    Full Text Available The present work reports the preparation of binderless carbon-coated porous films and the study of their performance as monolithic bioanodes. The films were prepared by coating anodic aluminum oxide (AAO films with a thin layer of nitrogen-doped carbon by chemical vapor deposition. The films have cylindrical straight pores with controllable diameter and length. These monolithic films were used directly as bioelectrodes by loading the films with D-fructose dehydrogenase (FDH, an oxidoreductase enzyme that catalyzes the oxidation of D-fructose to 5-keto-D-fructose. The immobilization of the enzymes was carried out by physical adsorption in liquid phase and with an electrostatic attraction method. The latter method takes advantage of the fact that FDH is negatively charged during the catalytic oxidation of fructose. Thus the immobilization was performed under the application of a positive voltage to the CAAO film in a FDH-fructose solution in McIlvaine buffer (pH 5 at 25 ºC. As a result, the FDH modified electrodes with the latter method show much better electrochemical response than that with the conventional physical adsorption method. Due to the singular porous structure of the monolithic films, which consists of an array of straight and parallel nanochannels, it is possible to rule out the effect of the diffusion of the D-fructose into the pores. Thus the improvement in the performance upon using the electrostatic attraction method can be ascribed not only to a higher uptake, but also to a more appropriate molecule orientation of the enzyme units on the surface of the electrodes.

  6. Improving the direct electron transfer in monolithic bioelectrodes prepared by immobilization of FDH enzyme on carbon-coated anodic aluminum oxide films

    Science.gov (United States)

    Castro-Muñiz, Alberto; Hoshikawa, Yasuto; Komiyama, Hiroshi; Nakayama, Wataru; Itoh, Tetsuji; Kyotani, Takashi

    2016-02-01

    The present work reports the preparation of binderless carbon-coated porous films and the study of their performance as monolithic bioanodes. The films were prepared by coating anodic aluminum oxide (AAO) films with a thin layer of nitrogen-doped carbon by chemical vapor deposition. The films have cylindrical straight pores with controllable diameter and length. These monolithic films were used directly as bioelectrodes by loading the films with D-fructose dehydrogenase (FDH), an oxidoreductase enzyme that catalyzes the oxidation of D-fructose to 5-keto-D-fructose. The immobilization of the enzymes was carried out by physical adsorption in liquid phase and with an electrostatic attraction method. The latter method takes advantage of the fact that FDH is negatively charged during the catalytic oxidation of fructose. Thus the immobilization was performed under the application of a positive voltage to the CAAO film in a FDH-fructose solution in McIlvaine buffer (pH 5) at 25 ºC. As a result, the FDH modified electrodes with the latter method show much better electrochemical response than that with the conventional physical adsorption method. Due to the singular porous structure of the monolithic films, which consists of an array of straight and parallel nanochannels, it is possible to rule out the effect of the diffusion of the D-fructose into the pores. Thus the improvement in the performance upon using the electrostatic attraction method can be ascribed not only to a higher uptake, but also to a more appropriate molecule orientation of the enzyme units on the surface of the electrodes.

  7. Optical Anisotropy and Porosity of Anodic Aluminum Oxide Characterized by Spectroscopic Ellipsometry

    NARCIS (Netherlands)

    Kooij, E. Stefan; Wormeester, Herbert; Galca, Aurelian C.; Poelsema, Bene

    2003-01-01

    Anodic oxidation of aluminum results in a mesoporous oxide film. The thin-film geometry of our samples enables straightforward optical modeling of ellipsometry spectra of fully anodized films, using only three physically relevant parameters. The system of randomly distributed, but aligned cylindrica

  8. Effect of heat treatment on bioactivity of anodic titania films

    International Nuclear Information System (INIS)

    Anodic oxidation could be employed to produce crystalline titania films on Ti6Al4 V surfaces for inducing apatite formation in simulated body fluid (SBF). In this work, the effect of further heat treatment on the bioactivity of anodic titania films was researched. The surface constitution, morphology, crystal structure and apatite-forming ability of titania films were characterized by X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM) and X-ray diffraction (XRD). The results indicated the apatite formation on the Ti6Al4 V surfaces could be attributed to abundance of Ti-OH groups formed via anodic oxidation, but subsequent heat treatment would decrease the amount of surface hydroxyl (OH) groups and result in the loss of the apatite-forming ability.

  9. Porous anodic film formation on an Al-3.5wt% Cu alloy

    Energy Technology Data Exchange (ETDEWEB)

    Paez, M. A.; Skeldon, P.; Thompson, G. E.; Saez, M.; Bustos, O.; Monsalve, A.

    2003-07-01

    The morphological development of porous anodic films in the initial stages is examined during anodizing an Al-3,5 wt% Cu alloy in phosphoric acid. Using transmission electron microscopy a sequence of ultramicrotomed anodic sections reveals the dynamic evolution of numerous features in the thickening film in the initial stages of anodizing. The morphological changes in the anodic oxides in the initial stages of its formation appears related to the formation of bubbles during film growth. From Rutherford backscattering spectroscopy (RBS) analysis of the film, the formation of the bubbles is associated with the enrichment of copper in the alloy due to growth of the anodic oxide. On the other hand, during constant current anodizing of Al-Cu in phosphoric acid, the current efficiency is considerably less than that for anodizing super pure aluminium under similar conditions. >From the contrasting results between the charge consumed calculated from RBS and the real charge consumed during anodizing, oxygen gas bubbles generation and copper oxidation seem to be of less importance on the low efficiency for film formation. It is apparent that the main cause of losing efficiency for film growth on Al-Cu is associated with generation of oxygen ar residual second phase, with the development of stresses in the film and, the consequence of these effects on film cracking during film growth. (Author) 10 refs.

  10. Research of the photovoltaic properties of anodized films of Sn

    Science.gov (United States)

    Afanasyev, D. A.; Ibrayev, N. Kh; Omarova, G. S.; Smagulov, Zh K.

    2015-04-01

    The results of studies of photovoltaic properties of solar cells based on porous tin oxide films, sensitized with an organic dye are presented. Porous films were prepared by electrochemical anodization of tin in alkaline electrolytes based on aqueous solution of NaOH and aqueous ammonia NH4OH. It was found that the time of anodizing of the Sn films affects on conversion efficiency of light energy into electrical energy. Increasing of the sorption time leads to an increase of the number of molecules on the surface of the porous film. For the solar cell based on tin oxide there is a strong dark current, which significantly reduces the efficiency of conversion of light energy into electrical energy.

  11. Excitation of anodized alumina films with a light source

    DEFF Research Database (Denmark)

    Aggerbeck, Martin; Canulescu, Stela; Rechendorff, K.;

    Optical properties of anodized aluminium alloys were determined by optical diffuse reflectance spectroscopy of such films. Samples with different concentrations of dopants were excited with a white-light source combined with an integrating sphere for fast determination of diffuse reflectance. The......, with doping are discussed. Using the Kubelka-Munk model on the diffuse reflectance spectra of such films, the bandgap Eg of the oxide alloys can be determined....

  12. Characterization and corrosion resistance of anodic electrodeposited titanium oxide/phosphate films on Ti-20Nb-10Zr-5Ta bioalloy

    Energy Technology Data Exchange (ETDEWEB)

    Popa, Monica; Vasilescu, Cora; Drob, Silviu I.; Osiceanu, Petre; Anastasescu, Mihai; Calderon-Moreno, Jose M., E-mail: josecalderonmoreno@yahoo.com [Institute of Physical Chemistry ' Ilie Murgulescu' of the Romanian Academy, Bucharest (Romania)

    2013-07-15

    In this work, the anodic galvanostatic electrodeposition of an oxidation film containing phosphates on Ti-20Nb-10Zr-5Ta alloy from orthophosphoric acid solution is presented. Its composition was determined by X-ray diffractometry (XRD), Fourier transform infrared spectroscopy (FTIR) and Raman micro-spectroscopy, and its topography by atomic force microscopy (AFM). The corrosion resistance of the coated alloy in simulated human fluid (by linear polarization method and monitoring of open circuit potentials, corresponding open circuit potential gradients) as well as the characterization of the coating (by Raman spectroscopy and depth profile X-ray photoelectron spectroscopy (XPS)) deposited in a period of 300 h soaking in simulated human body fluid were studied. The electrodeposited film was composed of amorphous titanium dioxide and contained phosphate groups. The corrosion resistance of the coated Ti-20Nb-10Zr-5Ta alloy in neutral and alkaline Ringer's solutions was higher than that of the bare alloy due to the protective properties of the electrodeposited film. The corrosion parameters improved over time as result of the thickening of the surface film by the deposition from the physiological solution. The deposited coating presented a variable composition in depth: at the deeper layer nucleated nanocrystalline hydroxyapatite and at the outer layer amorphous calcium phosphate. (author)

  13. Characterization and corrosion resistance of anodic electrodeposited titanium oxide/phosphate films on Ti-20Nb-10Zr-5Ta bioalloy

    International Nuclear Information System (INIS)

    In this work, the anodic galvanostatic electrodeposition of an oxidation film containing phosphates on Ti-20Nb-10Zr-5Ta alloy from orthophosphoric acid solution is presented. Its composition was determined by X-ray diffractometry (XRD), Fourier transform infrared spectroscopy (FTIR) and Raman micro-spectroscopy, and its topography by atomic force microscopy (AFM). The corrosion resistance of the coated alloy in simulated human fluid (by linear polarization method and monitoring of open circuit potentials, corresponding open circuit potential gradients) as well as the characterization of the coating (by Raman spectroscopy and depth profile X-ray photoelectron spectroscopy (XPS)) deposited in a period of 300 h soaking in simulated human body fluid were studied. The electrodeposited film was composed of amorphous titanium dioxide and contained phosphate groups. The corrosion resistance of the coated Ti-20Nb-10Zr-5Ta alloy in neutral and alkaline Ringer's solutions was higher than that of the bare alloy due to the protective properties of the electrodeposited film. The corrosion parameters improved over time as result of the thickening of the surface film by the deposition from the physiological solution. The deposited coating presented a variable composition in depth: at the deeper layer nucleated nanocrystalline hydroxyapatite and at the outer layer amorphous calcium phosphate. (author)

  14. X-ray reflectivity study of formation of multilayer porous anodic oxides of silicon.

    Energy Technology Data Exchange (ETDEWEB)

    Chu, Y.; Fenollosa, R.; Parkhutik, V.; You, H.

    1999-07-21

    The paper reports data on the kinetics of anodic oxide films growth on silicon in aqueous solutions of phosphoric acids as well as a study of the morphology of the oxides grown in a special regime of the oscillating anodic potential. X-ray reflectivity measurements were performed on the samples of anodic oxides using an intense synchrotron radiation source. They have a multilayer structure as revealed by theoretical fitting of the reflectivity data. The oscillations of the anodic potential are explained in terms of synchronized oxidation/dissolution reactions at the silicon surface and accumulation of mechanic stress in the oxide film.

  15. Effect of Pore Size and Film Thickness on Gold-Coated Nanoporous Anodic Aluminum Oxide Substrates for Surface-Enhanced Raman Scattering Sensor.

    Science.gov (United States)

    Kassu, Aschalew; Farley, Carlton; Sharma, Anup; Kim, Wonkyu; Guo, Junpeng

    2015-11-30

    A sensitive surface enhanced Raman scattering chemical sensor is demonstrated by using inexpensive gold-coated nanoporous anodic aluminum oxide substrates. To optimize the performance of the substrates for sensing by the Surface-enhanced Raman scattering (SERS) technique, the size of the nanopores is varied from 18 nm to 150 nm and the gold film thickness is varied from 30 nm to 120 nm. The sensitivity of gold-coated nanoporous surface enhanced Raman scattering sensor is characterized by detecting low concentrations of Rhodamine 6G laser dye molecules. The morphology of the SERS substrates is characterized by atomic force microscopy. Optical properties of the nanoporous SERS substrates including transmittance, reflectance, and absorbance are also investigated. Relative signal enhancement is plotted for a range of substrate parameters and a detection limit of 10(-6) M is established.

  16. Effect of Pore Size and Film Thickness on Gold-Coated Nanoporous Anodic Aluminum Oxide Substrates for Surface-Enhanced Raman Scattering Sensor

    Directory of Open Access Journals (Sweden)

    Aschalew Kassu

    2015-11-01

    Full Text Available A sensitive surface enhanced Raman scattering chemical sensor is demonstrated by using inexpensive gold-coated nanoporous anodic aluminum oxide substrates. To optimize the performance of the substrates for sensing by the Surface-enhanced Raman scattering (SERS technique, the size of the nanopores is varied from 18 nm to 150 nm and the gold film thickness is varied from 30 nm to 120 nm. The sensitivity of gold-coated nanoporous surface enhanced Raman scattering sensor is characterized by detecting low concentrations of Rhodamine 6G laser dye molecules. The morphology of the SERS substrates is characterized by atomic force microscopy. Optical properties of the nanoporous SERS substrates including transmittance, reflectance, and absorbance are also investigated. Relative signal enhancement is plotted for a range of substrate parameters and a detection limit of 10−6 M is established.

  17. Preparation of anodic films of stabilized zirconium at ambient temperature

    International Nuclear Information System (INIS)

    It was prepared zirconium oxide films through the anodic oxidation of the zirconium at constant current density in phosphoric acid solution.The film growth is characterized, at the cronopotenciograms curves, by linear increase of the potential and region of film breakdown, with potential oscillations. The films were analysed by x-rays and SEM. It was observed the formation of zirconia films in the monoclinic phase in H3 P O4 solution. When H3 P O4 was use with Na2 [Ca(EDTA)] complex were detected the formation of zirconium oxide partiality stabilized in the tetragonal cubic form. It was also observed that varying the concentration of the complex and the applied current density it was possible to obtain different quantity of the stabilized phase. (author)

  18. Self-ordering behavior of nanoporous anodic aluminum oxide (AAO) in malonic acid anodization

    Energy Technology Data Exchange (ETDEWEB)

    Lee, W; Nielsch, K; Goesele, U [Max Planck Institute of Microstructure Physics, Weinberg 2, D-06120 Halle (Germany)

    2007-11-28

    The self-ordering behavior of anodic aluminum oxide (AAO) has been investigated for anodization of aluminum in malonic acid (H{sub 4}C{sub 3}O{sub 4}) solution. In the present study it is found that a porous oxide layer formed on the surface of aluminum can effectively suppress catastrophic local events (such as breakdown of the oxide film and plastic deformation of the aluminum substrate), and enables stable fast anodic oxidation under a high electric field of 110-140 V and {approx}100 mA cm{sup -2}. Studies on the self-ordering behavior of AAO indicated that the cell homogeneity of AAO increases dramatically as the anodization voltage gets higher than 120 V. Highly ordered AAO with a hexagonal arrangement of the nanopores could be obtained in a voltage range 125-140 V. The current density (i.e., the electric field strength (E) at the bottom of a pore) is an important parameter governing the self-ordering of the nanopores as well as the interpore distance (D{sub int}) for a given anodization potential (U) during malonic acid anodization.

  19. Barrier and porous anodic oxides on InSb

    Energy Technology Data Exchange (ETDEWEB)

    Suleiman, A.; Hashimoto, T. [Corrosion and Protection Centre, School of Materials, University of Manchester, P.O. Box 88, Manchester M60 1QD (United Kingdom); Skeldon, P. [Corrosion and Protection Centre, School of Materials, University of Manchester, P.O. Box 88, Manchester M60 1QD (United Kingdom)], E-mail: peter.skeldon@manchester.ac.uk; Thompson, G.E. [Corrosion and Protection Centre, School of Materials, University of Manchester, P.O. Box 88, Manchester M60 1QD (United Kingdom); Echeverria, F. [Dpto de Ing. Metalurgica y de Materiales, Universidad de Antioquia, Oficina 18-240, Calle 67 No. 53-108, A.A. 1226, Medellin (Colombia); Graham, M.J.; Sproule, G.I.; Moisa, S. [Institute for Microstructural Sciences, National Research Council of Canada, Montreal Road, Ottawa, K1A 0R6 (Canada); Habazaki, H. [Graduate Engineering School, Hokkaido University, N13 W8, Kita-ku, Sapporo 060-8628 (Japan); Bailey, P.; Noakes, T.C.Q. [Daresbury Laboratory, Daresbury, Warrington WA4 4AD (United Kingdom)

    2008-05-15

    Anodizing of InSb at 5 mA cm{sup -2} in sodium tungstate electrolyte is shown to produce barrier-type amorphous oxide at relatively low voltages, to about 40 V, and porous-type amorphous oxide at increased voltages. The barrier-type amorphous oxide, consisting of units of In{sub 2}O{sub 3} and Sb{sub 2}O{sub 3}, distributed relatively uniformly throughout the film, develops at a formation ratio of 2.2 {+-} 0.2 nm V{sup -1}. The outer 15-20% of the film also contains tungsten species. The relatively high efficiency of barrier film growth reduces significantly with transition to porous oxide, which is associated additionally with generation of oxygen at the film surface. The final oxide, at 65 V, comprises pores, of typical diameter 80 nm, orientated approximately normal to the substrate and extending from a barrier region to the film surface.

  20. Wetting and Photocatalytic Properties of TiO2 Nanotube Arrays Prepared via Anodic Oxidation of E-Beam Evaporated Ti Thin Films

    Directory of Open Access Journals (Sweden)

    Soon Wook Kim

    2015-01-01

    Full Text Available TiO2 nanotube arrays (TNAs are fabricated on quartz substrate by anodizing E-beam evaporated Ti films. E-beam evaporated Ti films are directly anodized at various anodizing voltages ranging from 20 to 45 V and their morphological, wetting, and photocatalytic properties are examined. The photocatalytic activity of the prepared TNAs is evaluated by the photodecomposition of methylene blue under UV illumination. The TNAs prepared at an anodizing voltage of 30 V have a high roughness of 30.1 nm and a low water contact angle of 7.5°, resulting in a high photocatalytic performance. The surface roughness of the TNAs is found to correlate inversely with the water contact angle. High roughness (i.e., high surface area, which leads to high hydrophilicity, is desirable for effective photocatalytic activity.

  1. Features of the formation of anodic niobium oxide in a potassium nitrate melt

    Energy Technology Data Exchange (ETDEWEB)

    Skatkov, L.I.; Malyuk, Yu.I.

    1988-07-10

    This work is a further development of the investigations of the processes of the anodization of niobium in nitrate melts of salts at temperatures allowing recrystallization of the oxide. The anodic films of niobium formed in a nitrate melt consist of sandwiches of phases of Nb/sub 2/O/sub 5/, NbO/sub 2/, and NbO (from the outer surface of the anodic oxide film toward the niobium substrate), and high anodization temperatures cause the intense dissolution of oxygen in the niobium substrate. During the formation of an anodic oxide film, it becomes saturated with the anionic and cationic components of the electrolyte. The uptake of the anions is most significant in the initial stages of growth of the oxide layer, while saturation with potassium occurs in the final stages of anodization.

  2. Effect of intermetallic phases on the anodic oxidation and corrosion of 5A06 aluminum alloy

    Science.gov (United States)

    Li, Song-mei; Li, Ying-dong; Zhang, You; Liu, Jian-hua; Yu, Mei

    2015-02-01

    Intermetallic phases were found to influence the anodic oxidation and corrosion behavior of 5A06 aluminum alloy. Scattered intermetallic particles were examined by scanning electron microscopy (SEM) and energy dispersive spectroscopy (EDS) after pretreatment. The anodic film was investigated by transmission electron microscopy (TEM), and its corrosion resistance was analyzed by electrochemical impedance spectroscopy (EIS) and Tafel polarization in NaCl solution. The results show that the size of Al-Fe-Mg-Mn particles gradually decreases with the iron content. During anodizing, these intermetallic particles are gradually dissolved, leading to the complex porosity in the anodic film beneath the particles. After anodizing, the residual particles are mainly silicon-containing phases, which are embedded in the anodic film. Electrochemical measurements indicate that the porous anodic film layer is easily penetrated, and the barrier plays a dominant role in the overall protection. Meanwhile, self-healing behavior is observed during the long immersion time.

  3. Formation of Nanoporous Tin Oxide Layers on Different Substrates during Anodic Oxidation in Oxalic Acid Electrolyte

    Directory of Open Access Journals (Sweden)

    Leszek Zaraska

    2015-01-01

    Full Text Available Nanoporous tin oxide layers were obtained on various Sn substrates including high- and low-purity foils and wire by one-step anodic oxidation carried out in a 0.3 M oxalic acid electrolyte at various anodizing potentials. In general, amorphous oxide layers with the atomic ratio of Sn : O (1 : 1 were grown during anodization, and a typical structure of the as-obtained film consists of the “outer” layer with less regular, interconnetted pores and the “inner” layer with much more uniform and regular channels formed as a result of vigorous gas evolution. It was found that the use of electrochemical cell with the sample placed horizontally on the metallic support and stabilized by the Teflon cover, instead of the typical two-electrode system with vertically arranged electrodes, can affect the morphology of as-obtained layers and allows fabrication of nanoporous oxides even at anodizing potentials up to 11 V. An average pore diameter in the “outer” oxide layer increases with increasing anodizing potential, and no significant effect of substrate purity on the structure of anodic film was proved, except better uniformity of the oxides grown on high-purity Sn. A strong linear relationship between the average steady-state current density and anodizing potential was also observed.

  4. Ultra-structural evaluation of an anodic oxidated titanium dental implant.

    Science.gov (United States)

    Yamagami, Akiyoshi; Nagaoka, Noriyuki; Yoshihara, Kumiko; Nakamura, Mariko; Shirai, Hajime; Matsumoto, Takuya; Suzuki, Kazuomi; Yoshida, Yasuhiro

    2014-01-01

    Anodic oxidation is used for the surface treatment of commercial implants to improve their functional properties for clinical success. Here we conducted ultrastructural and chemical investigations into the micro- and nanostructure of the anodic oxide film of a titanium implant. The anodic oxidized layer of a Ti6Al4V alloy implant was examined ultrastructurally by transmission electron microscopy (TEM) and scanning electron microscopy (SEM). They were also analyzed using energy dispersive X-ray spectrometry (EDS) and X-ray photoelectron spectroscopy (XPS). The TEM revealed that the oxide layer of the Ti6Al4V implant prepared through anodic oxidation was separated into two layers. Al and V were not present on the top surface of the anodic oxide. This can be attributed to the biocompatibility of the anodic oxidized Ti6Al4V alloy implant, because the release of harmful metal ions such as Al and V can be suppressed by the biocompatibility. PMID:25483382

  5. Anodic oxide growth on Zr in neutral aqueous solution

    Indian Academy of Sciences (India)

    Z Tun; J J Noël; D W Shoesmith

    2008-10-01

    Anodization and subsequent cathodic reactions on a thin-film sample of Zr were studied with in-situ neutron reflectometry (NR) and electrochemical impedance spectroscopy (EIS). The NR results during anodization showed the originally 485 Å thick Zr film generally behaved similar to a bulk electrode in neutral solution. The anodization ratio measured at applied potentials increased in steps of 0.5 V was somewhat higher than the value determined by coulometry, while the Pilling Bedworth ratio is in good agreement with published data. Thickening of the oxide layer, accelerated immediately after each potential increase, gradually decreased over several hours, but remained non-zero even after ∼ 12 h. The thickened oxide eventually cracked when its thickness reached ∼ 120 Å, causing loss of passivation. Surprisingly, neither the anodization ratio nor the Pilling Bedworth ratio showed any discontinuity at the time of oxide cracking, and the EIS behaviour remained qualitatively as before. This observation is taken as the evidence that the cracked and intact regions of the electrode behave more or less independently as parallel electrodes. When the potential was eventually switched to cathodic polarity, NR shows, as expected, that the effects of oxide cracking were irreversible. However, the electrode resistance recovered partially suggesting the cracks were rapidly plugged with newly formed oxide.

  6. Visible light photo response from N-doped anodic niobium oxide after annealing in ammonia atmosphere

    International Nuclear Information System (INIS)

    Niobium oxide films with a thickness of approximately 165 nm were prepared by electrochemical anodization. These anodic oxide layers were then treated in an ammonia atmosphere at different temperatures and durations, and characterized with XRD, XPS, ToF-SIMS and photoelectrochemical methods. Under optimized conditions nitrogen doping of the niobium oxide films takes place, resulting in a distinct photo response in the visible range of light.

  7. Formation of Anodic Aluminum Oxide with Branched and Meshed Pores.

    Science.gov (United States)

    Kim, Byeol; Lee, Jin Seok

    2016-06-01

    Anodic aluminum oxide (AAO), with a self-ordered hexagonal array, is important for various applications in nanofabrication including as the fabrication of nanotemplates and other nanostructures. With the consideration, there have been many efforts to control the characteristic parameters of porous anodic alumina by adjustment of the anodizing conditions such as the electrolyte, temperature, applied potential, and Al purity. In particular, impurities in Al are changing the morphology of an alumina film; however, the formation mechanism has not yet been explained. In this work, we anodized a high purity (99.999%, Al(high)) and low purity (99.8%, Al(low)) aluminum foil by a two-step anodization process in an oxalic acid solution or phosphoric acid. It was found that the purity of aluminum foil has influenced the morphology of the alumina film resulting in branched and meshed pores. Also, electrochemical analysis indicated that the branched and meshed pores in the low-purity Al foil formed by the presence of impurities. Impurities act as defects and change the general growth mechanism for pore formation by inducing an electric field imbalance during anodization. This work contributes to the research field of topographical chemistry and applied fields including nanofabrication. PMID:27427755

  8. Self-Organizing Evolution of Anodized Oxide Films on Ti-25Nb-3Mo-2Sn-3Zr Alloy and Hydrophilicity

    Institute of Scientific and Technical Information of China (English)

    何芳; 李立军; 陈利霞; 李凤娇; 黄远

    2014-01-01

    In the present work, hierarchical nanostructured titanium dioxide (TiO2) films were fabricated on Ti-25Nb-3Mo-2Sn-3Zr (TLM) alloy for biomedical applications via one-step anodization process in ethylene glycol-based electrolyte containing 0.5wt%NH4F. The nanostructured TiO2 films exhibited three distinct types depending on the anodization time:top irregular nanopores (INP)/beneath regular nanopores (RNP), top INP/middle regular nano-tubes (RNT)/bottom RNP and top RNT with underlying RNP. The evolution of the nanostructured TiO2 films with anodization time demonstrated that self-organizing nanopores formed at the very beginning and individual nanotubes originated from underlying nanopore dissolution. Furthermore, a modified two-stage self-organizing mechanism was introduced to illustrate the growth of the nanostructured TiO2 films. Compared with TLM titanium alloy matrix, the TiO2 films with special nano-structure hold better hydrophilicity and higher specific surface area, which lays the foun-dation for their biomedical applications.

  9. Preparation of self-organized porous anodic niobium oxide microcones and their surface wettability

    International Nuclear Information System (INIS)

    Porous anodic niobium oxide with a pore size of ∼10 nm was formed at 10 V in glycerol electrolyte containing 0.6 mol dm-3 K2HPO4 and 0.2 mol dm-3 K3PO4 at 433 K. After prolonged anodizing for 5.4 ks, niobium oxide microcones develop on the surface. X-ray diffraction patterns of the anodized specimens revealed that the initially formed anodic oxide is amorphous, but an amorphous-to-crystalline transition occurs during anodizing. As a consequence of the preferential chemical dissolution of the initially formed amorphous oxide, due to different solubility of the amorphous and crystalline oxides, crystalline oxide microcones appear on the film surface after prolonged anodizing. The surface is superhydrophilic. After coating with fluorinated alkylsilane, the surface becomes superhydrophobic with a contact angle of 158o for water. The surface is also oil repellent, with a contact angle as high as 140o for salad oil.

  10. Fabrication of superhydrophobic niobium pentoxide thin films by anodization

    International Nuclear Information System (INIS)

    We report a simple method to fabricate a niobium oxide film with a lotus-like micro–nano surface structure. Self-assembled niobium pentoxide (Nb2O5) films with superhydrophobic property were fabricated by an anodization and a hydrophobic treatment. This process has several advantages such as low cost, simplicity and easy coverage of a large area. The surface of fabricated Nb2O5 film was changed from hydrophilic to superhydrophobic surface by a treatment using fluoroaldyltrimethoxysilane (FAS) solution. This value is considered to be the lowest surface free energy of any solid, based on the alignment of -CF3 groups on the surface. In particular, among FAS coated surfaces, the micro–nano complex cone structured Nb2O5 film showed the highest water-repellent property with a static contact angle of ca. 162°. This study gives promising routes from biomimetic superhydrophobic surfaces.

  11. The Microstructure and Capacitance Characterizations of Anodic Titanium Based Alloy Oxide Nanotube

    OpenAIRE

    Po Chun Chen; Sheng Jen Hsieh; Chien Chon Chen; Jun Zou

    2013-01-01

    This paper presents a simple anodization process to fabricate ordered nanotubes (NTs) of titanium and its alloys (Ti-Mo and Ti-Ta). TiO2, MoO3, and Ta2O5 are high dielectric constant materials for ultracapacitor application. The anodic titanium oxide contains a compact layer on the NT film and a barrier layer under the NT film. However, the microstructure of oxide films formed by anodic Ti-Mo and Ti-Ta alloys contains six layers, including a continuous compact layer, a continuous partial poro...

  12. Investigation of anodic oxide coatings on zirconium after heat treatment

    International Nuclear Information System (INIS)

    Highlights: • Oxide layers prepared via PEO of zirconium were subjected to heat treatment. • Surface characteristics were determined for the obtained oxide coatings. • Heat treatment led to the partial destruction of the anodic oxide layer. • Pitting corrosion resistance of zirconium was improved after the modification. - Abstract: Herein, results of heat treatment of zirconium anodised under plasma electrolytic oxidation (PEO) conditions at 500–800 °C are presented. The obtained oxide films were investigated by means of SEM, XRD and Raman spectroscopy. The corrosion resistance of the zirconium specimens was evaluated in Ringer's solution. A bilayer oxide coatings generated in the course of PEO of zirconium were not observed after the heat treatment. The resulting oxide layers contained a new sublayer located at the metal/oxide interface is suggested to originate from the thermal oxidation of zirconium. The corrosion resistance of the anodised metal was improved after the heat treatment

  13. Accounting for the Dynamic Oxidative Behavior of Nickel Anodes.

    Science.gov (United States)

    Smith, Rodney D L; Berlinguette, Curtis P

    2016-02-10

    The dynamic behavior of the anodic peak for amorphous nickel oxy/hydroxide (a-NiOx) films in basic media was investigated. Chronocoulometry of films with known nickel concentrations reveals that a total of four electrons per nickel site comprise the signature anodic peak at 1.32 V during the first oxidative scan, and two electrons are passed through the associated cathodic peak on the reverse scan. The anodic and cathodic signals each contain two electrons on the successive scans. Catalytic oxygen evolution reaction (OER) was detected within the anodic peak, which is at a lower potential than is widely assumed. In order to rationalize these experimental results, we propose that the four-electron oxidation event is the conversion of the film from nickel(II) hydroxide ([Ni(II)-OH](-)) to a higher valent nickel peroxide species (e.g., Ni(IV)-OO or Ni(III)-OO·). The subsequent reduction of the nickel peroxide species is confined by a chemical step resulting in the accumulation of [Ni(II)-OOH](-), which is then oxidized by two electrons to form Ni(IV)-OO during the subsequent oxidative scan on the time scale of a cyclic voltammetric experiment. Our proposed mechanism and the experimental determination that each nickel site is oxidized by four electrons helps link the myriad of seemingly disparate literature data related to OER catalysis by nickel electrodes. The faster catalysis that occurs at higher oxidative potentials is derived from a minority species and is not elaborated here. PMID:26829375

  14. Fabrication of anode-supported zirconia thin film electrolyte based core-shell particle structure for intermediate temperature solid oxide fuel cells

    Institute of Scientific and Technical Information of China (English)

    Peng Li; John T.S.Irvinen

    2013-01-01

    With a view to produce intermediate temperature SOFCs, yttria and scandia doped zirconia with a core-shell structure was prepared, then an anode supported fuel cell was fabricated by a spray method. The influences of the scandia content in the electrolyte and atmosphere conditions used in the testing experiments on phase composition, microstructure and fuel cell performance were investigated. The electrolyte was composed of cubic and tetragonal phases and SEM pictures revealed very fine grain sizes and a smooth surface of the electrolyte film, though some defects were observed in samples with high Scandia content. Coating scandia on partially stabilized zirconium particles improves both ionic conductivity of the electrolyte and power density of the fuel cell distinctly below 750 1C. Anodes were pre-sintered at 1200 1C before co-sintering with the electrolyte film to ensure that the shrinkage percentage was close to that of the electrolyte during co-sintering, avoiding warping of cell.

  15. Temperature dependence of electric resistance of anodic oxide films on niobium base alloy NbTsU

    International Nuclear Information System (INIS)

    Electrical resistance of oxide coatings formed on the surface of the NbTsU niobium alloy in aqueous solutions of alkaline electrolytes is investigated. Some anomalies related to the conditions of coating formation are canceled in temperature dependences of electrical resistance. The values of activation energy of electroconducting processes for different temperature intervals are calculated

  16. Metal-insulator transition in nanocomposite VOx films formed by anodic electrodeposition

    OpenAIRE

    Tsui, Lok-kun; Hildebrand, Helga; Lu, Jiwei; Schmuki, Patrik; Zangari, Giovanni

    2014-01-01

    The ability to grow VO2 films by electrochemical methods would open a low-cost, easily scalable production route to a number of electronic devices. We have synthesized VOx films by anodic electrodeposition of V2O5, followed by partial reduction by annealing in Ar. The resulting films are heterogeneous, consisting of various metallic/oxide phases and including regions with VO2 stoichiometry. A gradual metal insulator transition with a nearly two order of magnitude change in film resistance is ...

  17. In situ scanning tunneling microscopy study of the structure of the hydroxylated anodic oxide film formed on Cr(110) single-crystal surfaces

    Energy Technology Data Exchange (ETDEWEB)

    Zuili, D.; Maurice, V.; Marcus, P. [Ecole Nationale Superieure de Chimie de Paris (France)

    1999-09-16

    The structure of hydroxylated oxide films (passive films) formed on Cr(110) in 0.5 M H{sub 2}SO{sub 4} at +0.35, +0.55, and +0.75 V/SHE has been investigated by in situ scanning tunneling microscopy (STM). Cathodic reduction pretreatments at {minus}0.54, {minus}0.64, and {minus}0.74 V/SHE destroy the well-defined topography of the single-crystal electrode and they have been excluded from the passivation procedure. Two different passive film structures have been observed, depending on the potential and time of passivation. At low potential (+0.35 V/SHE), the passive film, consisting mostly of chromium hydroxide, has a noncrystalline and granular structure whose roughness suggests local variations of thickness of ca. {+-} 0.5 nm. A similar structure is observed at higher potential (+0.55 V/SHE), but only for a short polarization time. For longer polarization at 0.55 V/SHE, and at higher potentials (+0.75 V/SHE), a crystalline structure is formed; the higher the potential, the faster the crystallization. It corresponds to the growth of a chromium oxide layer in the passive film. This chromium oxide layer is (0001) oriented. A structural model of the passive film is proposed, with termination of this oxide layer by a monolayer of hydroxyl groups or of chromium hydroxide in (1 {times} 1) epitaxy with the underlying oxide, and with surface steps resulting from the emergence of stacking faults of the Cr{sup 3+} planes in the oxide layer. Energy band models of the electronic structure of the semiconductive passive films show that the tunneling mechanism of the STM imaging involves empty electronic states located in the band gap of the passive film. The growth of the oxide layer in the passive film is governed by a combined reaction of dehydration of chromium hydroxide and oxidation of chromium: Cr(OH){sub 3} (film) + Cr (metal) {yields} Cr{sub 2}O{sub 3} (film) + 3 H{sup +} + 3 e{sup {minus}}.

  18. Study of oxide films on the surface of cadmium telluride

    International Nuclear Information System (INIS)

    Study of oxide films on surfaces of CdTe monocrystals is continued by methods of ellipsometry and by absorption in IR-spectral range. Index values of refruction of oxide films, produced by cadmium telluride oxidation in hydrogen peroxide solutions, in oxigen flow at 673 K and by anode oxidation, as a rule, differ essentially in dependence on method of production, that gives evidence of differences in these films composition. Oxide films, produced in oxygen flow, as opposed to films, produced by two other methods, have intensive absorption, characteristic for tellurite group. Film thickness, produced by oxidation in hydrogen peroxide and in oxygen flow, varies within rather wide limits with observance of externally similar conditions of production. By contrast to it, thickness of anode films is regulated reliably by anode potential

  19. An Analysis of Mechanical Properties of Anodized Aluminum Film at High Stress

    Science.gov (United States)

    Zhao, Xixi; Wei, Guoying; Yu, Yundan; Guo, Yuemei; Zhang, Ao

    2015-10-01

    In this paper, a new environmental-friendly electrolyte containing sulfuric acid and tartaric acid has been used as the substitute of chromic acid for anodization. The work discussed the influence of anodizing voltages on the fatigue life of anodized Al 2024-T3 by performing fatigue tests with 0.1 stress ratio (R) at 320 MPa. Meanwhile the fatigue cycles to failure, yield strength, tensile strength and fracture surface of anodic films at different conditions were investigated. The results showed that the fatigue life of anodized and sealed specimens reduced a lot compared to aluminum alloy, which can be attributed to the crack sites initiated at the oxide layer. The fracture surface analyses also revealed that the number of crack initiation sites enlarged with the increase of anodizing voltage.

  20. Improving high voltage stability of lithium cobalt oxide/graphite battery via forming protective films simultaneously on anode and cathode by using electrolyte additive

    International Nuclear Information System (INIS)

    Highlights: • The cyclic stability of LiCoO2/graphite battery in voltage range of 3.0-4.5 V is improved by VEC. • VEC inhibits dimension change of the battery after cycling at 4.5 V cutoff voltage. • The SEI formed by VEC on cathode is able to inhibit the cobalt dissolution. • The anodic SEI formed by VEC suppresses the cobalt deposition and the electrolyte decomposition. - Abstract: We report a new finding that high voltage stability of lithium cobalt oxide (LiCoO2)/graphite battery can be improved by using vinyl ethylene carbonate (VEC) as an electrolyte additive. Charge/discharge tests demonstrate that the battery using VEC exhibits significantly improved cyclic and dimensional stability of the 053048-type LiCoO2/graphite pouch cell up to 4.5 V. The capacity retention is 87.0% and the swell value in thickness is 3.1% for the cell with 2.0 wt.% VEC after 400 cycles between 3.0 V and 4.5 V, compared to the values of 38.4% and 38.6%, respectively, for the cell without additive. The characterizations from scanning electron spectroscopy and X-ray photoelectron spectroscopy demonstrate that VEC facilitates the formation of stable solid electrolyte interfaces simultaneously on anode and cathode of the LiCoO2/graphite battery, yielding effective protections for anode and cathode and preventions of the electrolyte decomposition on both electrodes

  1. Effects of the voltage and time of anodization on modulation of the pore dimensions of AAO films for nanomaterials synthesis

    Science.gov (United States)

    Chahrour, Khaled M.; Ahmed, Naser M.; Hashim, M. R.; Elfadill, Nezar G.; Maryam, W.; Ahmad, M. A.; Bououdina, M.

    2015-12-01

    Highly-ordered and hexagonal-shaped nanoporous anodic aluminum oxide (AAO) of 1 μm thickness of Al pre-deposited onto Si substrate using two-step anodization was successfully fabricated. The growth mechanism of the porous AAO film was investigated by anodization current-time behavior for different anodizing voltages and by visualizing the microstructural procedure of the fabrication of AAO film by two-step anodization using cross-sectional and top view of FESEM imaging. Optimum conditions of the process variables such as annealing time of the as-deposited Al thin film and pore widening time of porous AAO film were experimentally determined to obtain AAO films with uniformly distributed and vertically aligned porous microstructure. Pores with diameter ranging from 50 nm to 110 nm and thicknesses between 250 nm and 1400 nm, were obtained by controlling two main influential anodization parameters: the anodizing voltage and time of the second-step anodization. X-ray diffraction analysis reveals amorphous-to-crystalline phase transformation after annealing at temperatures above 800 °C. AFM images show optimum ordering of the porous AAO film anodized under low voltage condition. AAO films may be exploited as templates with desired size distribution for the fabrication of CuO nanorod arrays. Such nanostructured materials exhibit unique properties and hold high potential for nanotechnology devices.

  2. Anodic deposition of hydrous ruthenium oxide for supercapacitors

    Science.gov (United States)

    Hu, Chi-Chang; Liu, Ming-Jue; Chang, Kuo-Hsin

    This communication demonstrates the success in the anodic deposition of hydrous ruthenium oxide (denoted as RuO 2· xH 2O) from RuCl 3· xH 2O in aqueous media with/without adding acetate ions (CH 3COO -, AcO -) as the complex agent. The benefits of as-deposited RuO 2· xH 2O include the low electron-hopping resistance and the low contact resistance at the Ti-RuO 2· xH 2O interface which are clarified in electrochemical impedance spectroscopic (EIS) studies. The cycling stability, specific capacitance, and power performance of as-deposited RuO 2· xH 2O are further improved by annealing in air at 150 °C for 2 h. The morphologies of as-deposited and annealed RuO 2· xH 2O films, examined by scanning electron microscopy (SEM), are very similar to that of thermally decomposed RuO 2. The high onset frequencies of 660 and 1650 Hz obtained from EIS spectra for the as-deposited and annealed RuO 2· xH 2O films, respectively, definitely illustrate the high-power merits of both oxide films prepared by means of the anodic deposition without considering the advantages of its simplicity, one-step, reliability, low cost, and versatility for electrode preparation.

  3. Influence of a platinum functional layer on a Ni-Ce{sub 0.9}Gd{sub 0.1}O{sub 1.95} anode for thin-film solid oxide fuel cells

    Energy Technology Data Exchange (ETDEWEB)

    Kang, Sungmin; Cha, Suk Won, E-mail: ybkim@hanyang.ac.kr, E-mail: swcha@snu.ac.kr [Department of Mechanical and Aerospace Engineering, Seoul National University, Gwanak-ro 1, Gwanak-gu, Seoul 151-744 (Korea, Republic of); Chang, Ikwhang [Graduate School of Convergence Science and Technology, Seoul National University, 864-1, Iui-dong, Yeongtong-gu, Suwon, Gyeonggi-do 443-270 (Korea, Republic of); Kim, Young-Beom, E-mail: ybkim@hanyang.ac.kr, E-mail: swcha@snu.ac.kr [Department of Mechanical Engineering, Hanyang University, 222 Wangshimni-ro, Seongdong-gu, Seoul 133-791 (Korea, Republic of)

    2015-09-15

    A Pt functional layer was deposited between a Ni-Ce{sub 0.9}Gd{sub 0.1}O{sub 1.95} (50 wt. % Ni) anode and an 8 mol. % yttria-stabilized zirconia electrolyte in order to enhance the performance of a thin film solid oxide fuel cell. By inserting this ultrathin functional layer, the ohmic impedance of the single cell was significantly reduced, and the maximum power density was increased by a factor of ∼1.55. However, excessive deposition of the Pt functional layer caused ionic conduction pathway blocking between the yttria-stabilized zirconia and Ni-Gd{sub 0.1}Ce{sub 0.9}O{sub 1.95} (Ni-GDC), deactivating the Ni-GDC as a mixed ionic and electronic conducting anode. As a result, both the ohmic impedance and anodic faradaic impedance were increased after introduction of excessive Pt functional layer, and the maximum power density was also reduced.

  4. On some peculiarities of surface properties of niobium anodic oxide crystals

    OpenAIRE

    Gomozov, V.; Deribo, S.; Tulskiy, G.; Skatkov, L.

    2012-01-01

    Changes in surface properties of anodic crystal films Nb2O5 during the extraction of oxygen anions from near-surface layer are considered. It is shown that the anion extraction brings about a phase transition in oxide which is accompanied by a change in conductivity resulting from structure distortion occurring during disordering in oxide crystals.

  5. Fabrication of superhydrophobic niobium pentoxide thin films by anodization

    Energy Technology Data Exchange (ETDEWEB)

    Jeong, Bong-Yong [Future Convergence Ceramic Division, Korea Institute of Ceramic Engineering and Technology, Seoul 153-801 (Korea, Republic of); Jung, Eun-Hye [Future Convergence Ceramic Division, Korea Institute of Ceramic Engineering and Technology, Seoul 153-801 (Korea, Republic of); Department of Chemical Engineering, Inha University, Incheon 402-024 (Korea, Republic of); Kim, Jin-Ho, E-mail: jhkim@kicet.re.kr [Electronic and Optic Materials Division, Korea Institute of Ceramic Engineering and Technology, Seoul 153-801 (Korea, Republic of)

    2014-07-01

    We report a simple method to fabricate a niobium oxide film with a lotus-like micro–nano surface structure. Self-assembled niobium pentoxide (Nb{sub 2}O{sub 5}) films with superhydrophobic property were fabricated by an anodization and a hydrophobic treatment. This process has several advantages such as low cost, simplicity and easy coverage of a large area. The surface of fabricated Nb{sub 2}O{sub 5} film was changed from hydrophilic to superhydrophobic surface by a treatment using fluoroaldyltrimethoxysilane (FAS) solution. This value is considered to be the lowest surface free energy of any solid, based on the alignment of -CF{sub 3} groups on the surface. In particular, among FAS coated surfaces, the micro–nano complex cone structured Nb{sub 2}O{sub 5} film showed the highest water-repellent property with a static contact angle of ca. 162°. This study gives promising routes from biomimetic superhydrophobic surfaces.

  6. Electrochromism of amorphous ruthenium oxide thin films

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Se-Hee; Liu, Ping; Tracy, C. Edwin; Deb, Satyen K. [National Renewable Energy Laboratory, Center for Basic Sciences, 1617 Cole Boulevard, Golden, CO 80401 (United States); Cheong, Hyeonsik M. [Sogang University, Shinsoo-Dong, Seoul 121-742 (Korea, Republic of)

    2003-12-01

    We report on the electrochromic behavior of amorphous ruthenium oxide thin films and their electrochemical characteristics for use as counterelectrodes for electrochromic devices. Hydrous ruthenium oxide thin films were prepared by cyclic voltammetry on ITO coated glass substrates from an aqueous ruthenium chloride solution. The cyclic voltammograms of this material show the capacitive behavior including two redox reaction peaks in each cathodic and anodic scan. The ruthenium oxide thin film electrode exhibits a 50% modulation of optical transmittance at 670 nm wavelength with capacitor charge/discharge.

  7. Characterization of titanium thin films anodically grown in phosphoric acid; Caracterisation des films d'oxyde de titane obtenus anodiquement dans l'acide phosphorique

    Energy Technology Data Exchange (ETDEWEB)

    Khadiri, M.E.; Benyaich [Faculte des Sciences Semlalia, Lab. d' Electrochimie et Chimie Analytique, Marakech (Morocco); Oueriagli, A.; Outzourhit, A.; Ameziane, E.L. [Faculte des Sciences Semlalia, Lab. de Physique du Solide et des Couches Minces, Marakech (Morocco)

    2004-08-01

    Ti-Cu(2%) alloy was anodized in a 5 M phosphoric acid solution under various voltages ranging from 10 to 35 V. The composition, the structural and optical properties of the as-grown oxide films were studied. It was found that the color of the anodized substrates varied from yellow to blue depending on the anodizing voltage. The films formed on the alloy are amorphous and the oxidation state of Ti on their surface is mainly +4. On the other hand it was found that the thickness of the films increases linearly with anodization voltage at rate of 1.94 nm/V, while the refractive index at the wavelength corresponding to the reflectance minimum was practically constant. These films were also found to have excellent protective properties for the examined alloy. (authors)

  8. Surface characteristics and electrochemical corrosion behavior of a pre-anodized microarc oxidation coating on titanium alloy.

    Science.gov (United States)

    Cui, W F; Jin, L; Zhou, L

    2013-10-01

    A porous bioactive titania coating on biomedical β titanium alloy was prepared by pre-anodization followed by micro arc oxidation technology. The effects of pre-anodization on the phase constituent, morphology and electrochemical corrosion behavior of the microarc oxidation coating were investigated. The results show that pre-anodization has less influence on the phase constituent and the surface morphology of the microarc oxidation coating, but improves the inner layer density of the microarc oxidation coating. The decrease of plasma discharge strength due to the presence of the pre-anodized oxide film contributes to the formation of the compact inner layer. The pre-anodized microarc oxidation coating effectively inhibits the penetration of the electrolyte in 0.9% NaCl solution and thus increases the corrosion resistance of the coated titanium alloy in physiological solution.

  9. Ordered Nanomaterials Thin Films via Supported Anodized Alumina Templates

    OpenAIRE

    Mohammed eES-SOUNI; Salah ehabouti

    2014-01-01

    Supported anodized alumina template films with highly ordered porosity are best suited for fabricating large area ordered nanostructures with tunable dimensions and aspect ratios. In this paper we first discuss important issues for the generation of such templates, including required properties of the Al/Ti/Au/Ti thin film heterostructure on a substrate for high quality templates. We then show examples of anisotropic nanostructure films consisting of noble metals using these templates, discus...

  10. Ordered Nanomaterial Thin Films via Supported Anodized Alumina Templates

    OpenAIRE

    Es-Souni, Mohammed; Habouti, Salah

    2014-01-01

    Supported anodized alumina template films with highly ordered porosity are best suited for fabricating large-area ordered nanostructures with tunable dimensions and aspect ratios. In this paper, we first discuss important issues for the generation of such templates, including required properties of the Al/Ti/Au/Ti thin-film heterostructure on a substrate for high-quality templates. We then show examples of anisotropic nanostructure films consisting of noble metals using these templates, discu...

  11. Study on the Rare Earth Sealing Procedure of the Porous Film of Anodized 2024 Aluminum Alloy

    Institute of Scientific and Technical Information of China (English)

    2003-01-01

    The rare earth sealing procedure of the porous film of anodized aluminum alloy 2024 was studied with the fieldemission scanning electron microscope (SEM) and X-ray energy dispersive spectroscopy (EDS). The results show thatRE solution can form cerium oxide/hydroxides precipitation in the pores of the anodized coating at the beginning ofsealing. At the same time, the spherical deposits formed on the surface of the anodized coating created a barrierto the precipitation of RE solution in the pores. When the pore-structured anodizing film is covered all with thespherical deposits, RE conversion coating will form on the surface of the anodized coating. The reaction of thecoating formation was investigated by employing cyclic voltammetry. The results indicate that accelerator H2O2 actsas the source of O2 by carrying chemical reaction in course of coating formation. In the mean time, it maybe carrieselectrochemical reaction to generate alkaline condition to accelerate the coating formation. The porous structure ofthe film is beneficial to the precipitation of the cerium hydroxides film.

  12. Nano structured porous anodized aluminium oxide by using C2H2O4 for electronic applications: Study of the cell potential effects on formation of porous alumina

    International Nuclear Information System (INIS)

    In this research, a nano porous anodized aluminium oxide AAO thin film was successfully grown onto oxide layer on silicon substrate. The anodization of Si/ SiO2/ Al substrate was conducted in a vigorous stirring oxalic acid bath solution. The rate of growth, morphology and also the kinetic study of the AAO thin film were investigated. The resulting array, pores structure and pores density of AAO strongly depends on an applied voltage of the anodizing process. (author)

  13. Preparation and properties of antimony thin film anode materials

    Institute of Scientific and Technical Information of China (English)

    SU Shufa; CAO Gaoshao; ZHAO Xinbing

    2004-01-01

    Metallic antimony thin films were deposited by magnetron sputtering and electrodeposition. Electrochemical properties of the thin film as anode materials for lithium-ion batteries were investigated and compared with those of antimony powder. It was found that both magnetron sputtering and electrodeposition are easily controllable processes to deposit antimony films with fiat charge/discharge potential plateaus. The electrochemical performances of antimony thin films, especially those prepared with magnetron sputtering, are better than those of antimony powder. The reversible capacities of the magnetron sputtered antimony thin film are above 400 mA h g-1 in the first 15 cycles.

  14. Nanoporous of W/WO{sub 3} thin film electrode grown by electrochemical anodization applied in the photoelectrocatalytic oxidation of the basic red 51 used in hair dye

    Energy Technology Data Exchange (ETDEWEB)

    Fraga, Luciano E.; Zanoni, Maria Valnice B., E-mail: fraga@iq.unesp.b [Universidade Estadual Paulista (IQ/UNESP), Araraquara, SP (Brazil). Inst. de Quimica. Dept. de Quimica Analitica

    2011-07-01

    Self-organized W/WO{sub 3} nanoporous electrodes can be obtained by simple electrochemical anodization of W foil in 0.15 mol L{sup -1} NaF solution as the supporting electrolyte, applying a ramp potential of 0.2 V s{sup -1} until it reached 60 V, which was maintained for 2 h. The monoclinic form is majority in the highly ordered WO{sub 3} annealed at 450 deg C, obtaining a higher photoactivity when irradiated by visible light than by UV light. The electrode promotes complete discoloration of the investigated basic red 51 dye after 60 min of photoelectrocatalytic oxidation, on current density of 1.25 mA cm{sup -2} and irradiation on wavelength of 420-630 nm. In this condition it was obtained 63% of mineralization. Lower efficiency is obtained for the system irradiated by wavelength (280- 400 nm) when only 40% of total organic carbon removal is obtained and 120 min is required for complete discoloration. (author)

  15. Formation of Nanoporous Anodic Alumina by Anodization of Aluminum Films on Glass Substrates.

    Science.gov (United States)

    Lebyedyeva, Tetyana; Kryvyi, Serhii; Lytvyn, Petro; Skoryk, Mykola; Shpylovyy, Pavlo

    2016-12-01

    Our research was aimed at the study of aluminum films and porous anodic alumina (PAA) films in thin-film РАА/Al structures for optical sensors, based on metal-clad waveguides (MCWG). The results of the scanning electron microscopy (SEM) and atomic force microscopy (AFM) studies of the structure of Al films, deposited by DC magnetron sputtering, and of PAA films, formed on them, are presented in this work.The study showed that the structure of the Al films is defined by the deposition rate of aluminum and the thickness of the film. We saw that under anodization in 0.3 M aqueous oxalic acid solution at a voltage of 40 V, the PAA film with a disordered array of pores was formed on aluminum films 200-600 nm thick, which were deposited on glass substrates with an ultra-thin adhesive Nb layer. The research revealed the formation of two differently sized types of pores. The first type of pores is formed on the grain boundaries of aluminum film, and the pores are directed perpendicularly to the surface of aluminum. The second type of pores is formed directly on the grains of aluminum. They are directed perpendicularly to the grain plains. There is a clear tendency to self-ordering in this type of pores. PMID:27083584

  16. Formation of Ultrafine Metal Particles and Metal Oxide Precursor on Anodized Al by Electrolysis Deposition

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    Nickel was deposited by ac electrolysis deposition in the pores of the porous oxide film of Al produced by anodizing in phosphoric acid. Ultrafine rod-shaped Ni particles were formed in the pores. At the same time a film of Ni oxide precursor was developed on the surface of the porous oxide film. The Ni particles and the Ni oxide precursor were examined by SEM, TEM and X-ray diffraction. The thickness of the barrier layer of the porous oxide film was thin and it attributed to the formation of the metal particles, while the formation of the oxide precursor was associated with the surface pits which were developed in the pretreatment of Al.

  17. Redox Stable Anodes for Solid Oxide Fuel Cells

    Directory of Open Access Journals (Sweden)

    Guoliang eXiao

    2014-06-01

    Full Text Available Solid oxide fuel cells (SOFCs can convert chemical energy from the fuel directly to electrical energy with high efficiency and fuel flexibility. Ni-based cermets have been the most widely adopted anode for SOFCs. However, the conventional Ni-based anode has low tolerance to sulfur-contamination, is vulnerable to deactivation by carbon build-up (coking from direct oxidation of hydrocarbon fuels, and suffers volume instability upon redox cycling. Among these limitations, the redox instability of the anode is particularly important and has been intensively studied since the SOFC anode may experience redox cycling during fuel cell operations even with the ideal pure hydrogen as the fuel. This review aims to highlight recent progresses on improving redox stability of the conventional Ni-based anode through microstructure optimization and exploration of alternative ceramic-based anode materials.

  18. Air-Impregnated Nanoporous Anodic Aluminum Oxide Layers for Enhancing the Corrosion Resistance of Aluminum.

    Science.gov (United States)

    Jeong, Chanyoung; Lee, Junghoon; Sheppard, Keith; Choi, Chang-Hwan

    2015-10-13

    Nanoporous anodic aluminum oxide layers were fabricated on aluminum substrates with systematically varied pore diameters (20-80 nm) and oxide thicknesses (150-500 nm) by controlling the anodizing voltage and time and subsequent pore-widening process conditions. The porous nanostructures were then coated with a thin (only a couple of nanometers thick) Teflon film to make the surface hydrophobic and trap air in the pores. The corrosion resistance of the aluminum substrate was evaluated by a potentiodynamic polarization measurement in 3.5 wt % NaCl solution (saltwater). Results showed that the hydrophobic nanoporous anodic aluminum oxide layer significantly enhanced the corrosion resistance of the aluminum substrate compared to a hydrophilic oxide layer of the same nanostructures, to bare (nonanodized) aluminum with only a natural oxide layer on top, and to the latter coated with a thin Teflon film. The hydrophobic nanoporous anodic aluminum oxide layer with the largest pore diameter and the thickest oxide layer (i.e., the maximized air fraction) resulted in the best corrosion resistance with a corrosion inhibition efficiency of up to 99% for up to 7 days. The results demonstrate that the air impregnating the hydrophobic nanopores can effectively inhibit the penetration of corrosive media into the pores, leading to a significant improvement in corrosion resistance. PMID:26393523

  19. Air-Impregnated Nanoporous Anodic Aluminum Oxide Layers for Enhancing the Corrosion Resistance of Aluminum.

    Science.gov (United States)

    Jeong, Chanyoung; Lee, Junghoon; Sheppard, Keith; Choi, Chang-Hwan

    2015-10-13

    Nanoporous anodic aluminum oxide layers were fabricated on aluminum substrates with systematically varied pore diameters (20-80 nm) and oxide thicknesses (150-500 nm) by controlling the anodizing voltage and time and subsequent pore-widening process conditions. The porous nanostructures were then coated with a thin (only a couple of nanometers thick) Teflon film to make the surface hydrophobic and trap air in the pores. The corrosion resistance of the aluminum substrate was evaluated by a potentiodynamic polarization measurement in 3.5 wt % NaCl solution (saltwater). Results showed that the hydrophobic nanoporous anodic aluminum oxide layer significantly enhanced the corrosion resistance of the aluminum substrate compared to a hydrophilic oxide layer of the same nanostructures, to bare (nonanodized) aluminum with only a natural oxide layer on top, and to the latter coated with a thin Teflon film. The hydrophobic nanoporous anodic aluminum oxide layer with the largest pore diameter and the thickest oxide layer (i.e., the maximized air fraction) resulted in the best corrosion resistance with a corrosion inhibition efficiency of up to 99% for up to 7 days. The results demonstrate that the air impregnating the hydrophobic nanopores can effectively inhibit the penetration of corrosive media into the pores, leading to a significant improvement in corrosion resistance.

  20. Digital simulation of anodic stripping voltammetry from thin film electrodes

    International Nuclear Information System (INIS)

    The anodic stripping voltammetry (ASV) is routinely applied to control of Cu(II) in heavy water in the primary cooling loop of the Nuclear Power Reactor. The anodic stripping voltammetry (ASV) is a very well-known technique in electroanalytical chemistry. However, due to the complexity of the phenomena, it is practised with the fundamentals of empiric considerations. A geometric model for the anodic stripping voltammetry (ASV) from thin film electrodes which can be calculated by explicit digital simulation method is proposed as a possibility of solving the electrochemically reversible, cuasi-reversible and irreversible reactions under linear potential scan and multiple potential scans. (Until now the analytical mathematical method was applied to reversible reactions). All the results are compared with analytical solutions and experimental results and it permits to conclude that the anodic stripping voltammetry (ASV) can be studied with the simplicity and potentialities of explicit digital simulation methods. (M.E.L.)

  1. Fabrication of Nanostructured PLGA Scaffolds Using Anodic Aluminum Oxide Templates

    CERN Document Server

    Hsueh, Cheng-Chih; Hsu, Shan-Hui; Hung, Huey-Shan

    2008-01-01

    PLGA (poly(lactic-co-glycolic acid)) is one of the most used biodegradable and biocompatible materials. Nanostructured PLGA even has great application potentials in tissue engineering. In this research, a fabrication technique for nanostructured PLGA membrane was investigated and developed. In this novel fabrication approach, an anodic aluminum oxide (AAO) film was use as the template ; the PLGA solution was then cast on it ; the vacuum air-extraction process was applied to transfer the nano porous pattern from the AAO membrane to the PLGA membrane and form nanostures on it. The cell culture experiments of the bovine endothelial cells demonstrated that the nanostructured PLGA membrane can double the cell growing rate. Compared to the conventional chemical-etching process, the physical fabrication method proposed in this research not only is simpler but also does not alter the characteristics of the PLGA. The nanostructure of the PLGA membrane can be well controlled by the AAO temperate.

  2. CdSxSe1−x alloyed quantum dots-sensitized solar cells based on different architectures of anodic oxidation TiO2 film

    International Nuclear Information System (INIS)

    Nanostructured TiO2 translucent films with different architectures including TiO2 nanotube (NT), TiO2 nanowire (NW), and TiO2 nanowire/nanotube (NW/NT) have been produced by second electrochemical oxidization of TiO2 NT with diameter around 90–110 nm via modulation of applied voltage. These TiO2 architectures are sensitized with CdSxSe1−x alloyed quantum dots (QDs) in sizes of around 3–5 nm aiming to tune the response of the photoelectrochemical properties in the visible region. One-step hydrothermal method facilitates the deposition of CdSxSe1−x QDs onto TiO2 films. These CdSxSe1−x QDs exhibit a tunable range of light absorption with changing the feed molar ratio of S:Se in precursor solution, and inject electrons into TiO2 films upon excitation with visible light, enabling their application as photosensitizers in sensitized solar cells. Power conversion efficiency (PCE) of 2.00, 1.72, and 1.06 % are achieved with CdSxSe1−x (obtained with S:Se = 0:4) alloyed QDs sensitized solar cells based on TiO2 NW/NT, TiO2 NW, and TiO2 NT architectures, respectively. The significant enhancement of power conversion efficiency obtained with the CdSxSe1−x/TiO2 NW/NT solar cell can be attributed to the extended absorption of light region tuned by CdSxSe1−x alloyed QDs and enlarged deposition of QDs and efficient electrons transport provided by TiO2 NW/NT architecture

  3. Porous Anodic Aluminum Oxide with Serrated Nanochannels

    Science.gov (United States)

    Li, Dongdong; Zhao, Liang; Lu, Jia G.

    2010-03-01

    Self-assembled nanoporous anodic aluminum oxide (AAO) membrane with straight channels has long been an important tool in synthesizing highly ordered and vertically aligned quasi-1D nanostructures for various applications. Recently shape-selective nanomaterials have been achieved using AAO as a template. It is envisioned that nanowires with multi-branches will significantly increase the active functional sites for applications as sensors, catalysts, chemical cells, etc. Here AAO membranes with serrated nanochannels have been successfully fabricated via a two-step annodization method. The serrated channels with periodic intervals are aligned at an angle of ˜25^circ along the stem channels. The formation of the serrated channels is attributed to the evolution of oxygen gas bubbles and the resulted plastic deformation in oxide membrane. In order to reveal the inside channel structure, Platinum are electrodeposited into the AAO template. The as-synthesized serrated Pt nanowires demonstrate a superior electrocatalytic activity. This is attributed to the enhanced electric field strength around serrated tips as shown in the electric field simulation by COMOSL. Moreover, hierarchical serrated/straight hybrid structures can be constructed using this simple and novel self assembly technique.

  4. Surface of Alumina Films after Prolonged Breakdowns in Galvanostatic Anodization

    Directory of Open Access Journals (Sweden)

    Christian Girginov

    2011-01-01

    Full Text Available Breakdown phenomena are investigated at continuous isothermal (20∘C and galvanostatic (0.2–5 mA cm−2 anodizing of aluminum in ammonium salicylate in dimethylformamide (1 M AS/DMF electrolyte. From the kinetic (-curves, the breakdown voltage ( values are estimated, as well as the frequency and amplitude of oscillations of formation voltage ( at different current densities. The surface of the aluminum specimens was studied using atomic force microscopy (AFM. Data on topography and surface roughness parameters of the electrode after electric breakdowns are obtained as a function of anodization time. The electrode surface of anodic films, formed with different current densities until the same charge density has passed (2.5 C cm−2, was assessed. Results are discussed on the basis of perceptions of avalanche mechanism of the breakdown phenomena, due to the injection of electrons and their multiplication in the volume of the film.

  5. Electrocatalytic Materials and Techniques for the Anodic Oxidation of Various Organic Compounds

    Energy Technology Data Exchange (ETDEWEB)

    Stephen Everett Treimer

    2002-06-27

    The focus of this thesis was first to characterize and improve the applicability of Fe(III) and Bi(V) doped PbO{sub 2} film electrodes for use in anodic O-transfer reactions of toxic and waste organic compounds, e.g. phenol, aniline, benzene, and naphthalene. Further, they investigated the use of alternative solution/electrode interfacial excitation techniques to enhance the performance of these electrodes for remediation and electrosynthetic applications. Finally, they have attempted to identify a less toxic metal oxide film that may hold promise for future studies in the electrocatalysis and photoelectrocatalysis of O-transfer reactions using metal oxide film electrodes.

  6. Amperometric detection and electrochemical oxidation of aliphatic amines and ammonia on silver-lead oxide thin-film electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Ge, Jisheng

    1996-01-08

    This thesis comprises three parts: Electrocatalysis of anodic oxygen-transfer reactions: aliphatic amines at mixed Ag-Pb oxide thin-film electrodes; oxidation of ammonia at anodized Ag-Pb eutectic alloy electrodes; and temperature effects on oxidation of ethylamine, alanine, and aquated ammonia.

  7. Nanoporous anodic aluminum oxide with a long-range order and tunable cell sizes by phosphoric acid anodization on pre-patterned substrates

    Science.gov (United States)

    Surawathanawises, Krissada; Cheng, Xuanhong

    2014-01-01

    Nanoporous anodic aluminum oxide (AAO) has been explored for various applications due to its regular cell arrangement and relatively easy fabrication processes. However, conventional two-step anodization based on self-organization only allows the fabrication of a few discrete cell sizes and formation of small domains of hexagonally packed pores. Recent efforts to pre-pattern aluminum followed with anodization significantly improve the regularity and available pore geometries in AAO, while systematic study of the anodization condition, especially the impact of acid composition on pore formation guided by nanoindentation is still lacking. In this work, we pre-patterned aluminium thin films using ordered monolayers of silica beads and formed porous AAO in a single-step anodization in phosphoric acid. Controllable cell sizes ranging from 280 nm to 760 nm were obtained, matching the diameters of the silica nanobead molds used. This range of cell size is significantly greater than what has been reported for AAO formed in phosphoric acid in the literature. In addition, the relationships between the acid concentration, cell size, pore size, anodization voltage and film growth rate were studied quantitatively. The results are consistent with the theory of oxide formation through an electrochemical reaction. Not only does this study provide useful operational conditions of nanoindentation induced anodization in phosphoric acid, it also generates significant information for fundamental understanding of AAO formation. PMID:24535886

  8. Nanoporous anodic aluminum oxide with a long-range order and tunable cell sizes by phosphoric acid anodization on pre-patterned substrates.

    Science.gov (United States)

    Surawathanawises, Krissada; Cheng, Xuanhong

    2014-01-20

    Nanoporous anodic aluminum oxide (AAO) has been explored for various applications due to its regular cell arrangement and relatively easy fabrication processes. However, conventional two-step anodization based on self-organization only allows the fabrication of a few discrete cell sizes and formation of small domains of hexagonally packed pores. Recent efforts to pre-pattern aluminum followed with anodization significantly improve the regularity and available pore geometries in AAO, while systematic study of the anodization condition, especially the impact of acid composition on pore formation guided by nanoindentation is still lacking. In this work, we pre-patterned aluminium thin films using ordered monolayers of silica beads and formed porous AAO in a single-step anodization in phosphoric acid. Controllable cell sizes ranging from 280 nm to 760 nm were obtained, matching the diameters of the silica nanobead molds used. This range of cell size is significantly greater than what has been reported for AAO formed in phosphoric acid in the literature. In addition, the relationships between the acid concentration, cell size, pore size, anodization voltage and film growth rate were studied quantitatively. The results are consistent with the theory of oxide formation through an electrochemical reaction. Not only does this study provide useful operational conditions of nanoindentation induced anodization in phosphoric acid, it also generates significant information for fundamental understanding of AAO formation.

  9. Improvement of corrosion resistance of AZ31 Mg alloy by anodizing with co-precipitation of cerium oxide

    Institute of Scientific and Technical Information of China (English)

    Salah Abdelghany SALMAN; Ryoichi ICHINO; Masazumi OKIDO

    2009-01-01

    Anodizing of AZ31 Mg alloy in NaOH solution by co-precipitation of cerium oxide was investigated. The chemical composition and phase structure of the coating film were determined via optical microscopy, SEM and XRD. The corrosion properties of the anodic film were characterized by using potentiodynamic polarization curves in 17 mmol/L NaCl and 0.1 mol/L Na2SO4 solution at 298 K. The corrosion resistance of AZ31 magnesium alloy is significantly improved by adding cerium oxide to alkaline solution. In addition, the surface properties are enhanced and the film contains no crack.

  10. 二氧化钛纳米管阵列薄膜的超声辐射阳极氧化制备%Supersonic Anodization Preparation of Thin Titanium Oxide Nanotube Arrays Films

    Institute of Scientific and Technical Information of China (English)

    熊必涛; 朱志艳; 王长荣; 陈宝信; 骆钧炎

    2013-01-01

    通过使用铂片作为对电极在含有氢氟酸的二甲基亚砜溶液中,将金属钛片进行阳极氧化的方法制备得到二氧化钛纳米管阵列薄膜.在施加40 V偏压超声辐射作用下阳极氧化24 h条件下得到的二氧化钛纳米管长达到680nm,管内直径25 nm,管壁厚度约3~5 nm.采用了XRD和TEM等分析手段表征了二氧化钛纳米管阵列薄膜的微观结构和表面形貌,分别测试了薄膜的光吸收性能、循环伏安特性和光化学转换效率,并和碱性溶胶-凝胶方法制备的纳米晶二氧化钛薄膜作了对比研究.实验制备的二氧化钛纳米管阵列薄膜电极的光吸收率比纳米晶二氧化钛薄膜提高了40%,光电化学转换效率前者是后者的6倍,实验结果表明二氧化钛纳米管阵列薄膜结构有利于加快电子的传输,并能减少电荷复合,采用这种二氧化钛纳米管阵列薄膜结构的染料敏化太阳能电池光电极有望进一步提高太阳能电池的效率.本文还探讨了在超声波辐射作用下二氧化钛纳米管阵列薄膜的形成机理.%Thin titanium oxide nanotube arrays (TNAs) films were synthesized by supersonic anodization of titanium foil in an aqueous dimethyl sulfoxide solution containing HE After anodization, TNAs up to 680 nm in length, 25 nm inner pore diameter, and 3~5 nm wall thickness were obtained. Their microstructure and surface morphologies were characterized by XRD and TEM. The optical absorption performances, cyclic voltammograms characteristics and light chemical conversion efficiencies of these films were tested. The results implied that the TNAs films have an outstanding accelerated electronic transportation and compressed recombination rate. Electrodes applying such kind of titania nanotubes will have a potential to further enhance the TNAs-based dye-sensitized solar cells efficiencies. The sonoelectrochemical mechanism of TNAs films formation was discussed along with the characterization and

  11. Preparation and Properties of Al-Ni Composite Anodic Films on Aluminum Surface

    Institute of Scientific and Technical Information of China (English)

    ZHAO Xuhui; YE Hao; ZHANG Xiaofeng; ZUO Yu

    2012-01-01

    Ni element was introduced to aluminum surface by a simple chemical immersion method,and Al-Ni composite anodic films were obtained by following anodizing.The morphology,structure and composition of the Al-Ni anodic films were examined by scanning electron microscopy (SEM),energy disperse spectroscopy (EDS) and atomic force microscopy(AFM).The electrochemical behaviors of the films were studied by means of polarization measurement and electrochemical impedance spectroscopy (EIS).The experimental results show that the A1-Ni composite anodic film is more compact with smaller pore diameters than that of the Al anodic film.The introduction of nickel increases the impedances of both the barrier layer and the porous layer of the anodic films.In NaCl solutions,the Al-Ni composite anodic films show higher impedance values and better corrosion resistance.

  12. Microstructural Models of Alumina Nanotubes and Anodic Porous Alumina Film Formed in Sulphuric Acid

    Institute of Scientific and Technical Information of China (English)

    濮林; 陈志强; 谭超; 杨铮; 邹建平; 鲍希茂; 冯端; 施毅; 郑有蚪

    2002-01-01

    Electrochemical stepwise anodization of aluminium in dilute sulphuric acid results in the formation of alumina nanotubes (ANTs) due to the hexagonal split of the anodic porous alumina (APA) film along the cell boundaries containing many voids; that is, the ANTs are the completely detached cell of the APA film. The inner diameters of the ANTs are in the range of 10 - 20 nm, and the aspect ratio (inner diameter/length) of the ANTs can be about 80. The relations found for pore diameter, cell diameter and barrier layer thickness are around 1, 2.7 and 0.85 nm/V, respectively. Transmission electron microscopy (TEM) reveals that the ANT wall has a three-shell structure: an outer shell (metal/oxide interface) consisting of pure alumina oxide, a middle shell of the hydrated oxide or/and hydroxide and an inner shell (oxide/electrolyte interface) of anion incorporated oxide with the thickness ratio of 1:1:2. The structural change of ANTs induced by e-beam irradiation in TEM indicates that the thermal instability of the hydrated oxide or/and hydroxide within the cell wall might be an alternative origin contributing to the self-organization of the cells, leading to a densely packed triangular cell lattice of the APA film.

  13. Anodic oxides on InAlP formed in sodium tungstate electrolyte

    Energy Technology Data Exchange (ETDEWEB)

    Suleiman, A. [Corrosion and Protection Centre, School of Materials, University of Manchester, P.O. Box 88, Manchester M60 1QD (United Kingdom); Skeldon, P. [Corrosion and Protection Centre, School of Materials, University of Manchester, P.O. Box 88, Manchester M60 1QD (United Kingdom)], E-mail: p.skeldon@manchester.ac.uk; Thompson, G.E. [Corrosion and Protection Centre, School of Materials, University of Manchester, P.O. Box 88, Manchester M60 1QD (United Kingdom); Echeverria, F. [Corrosion and Protection Group, University of Antioquia, Medellin (Colombia); Graham, M.J.; Sproule, G.I.; Moisa, S.; Quance, T. [Institute for Microstructural Sciences, National Research Council of Canada, Montreal Road, Ottawa K1A 0R6 (Canada); Habazaki, H. [Graduate Engineering School, Hokkaido University, N13 W8, Kita-ku, Sapporo 060-8628 (Japan)

    2010-02-15

    Amorphous anodic oxide films on InAlP have been grown at high efficiency in sodium tungstate electrolyte. The films are shown to comprise an outer layer containing indium species, an intermediate layer containing indium and aluminium species and an inner layer containing indium, aluminium and phosphorus species{sub .} The layering correlates with the influence on cation migration rates of the energies of In{sup 3+}-O, Al{sup 3+}-O and P{sup 5+}-O bonds, which increase in this order. The film surface becomes increasingly rough with increase of the anodizing voltage as pores develop in the film, which appear to be associated with generation of oxygen gas.

  14. Metal-insulator transition in nanocomposite VOx films formed by anodic electrodeposition

    Science.gov (United States)

    Tsui, Lok-kun; Hildebrand, Helga; Lu, Jiwei; Schmuki, Patrik; Zangari, Giovanni

    2013-11-01

    The ability to grow VO2 films by electrochemical methods would open a low-cost, easily scalable production route to a number of electronic devices. We have synthesized VOx films by anodic electrodeposition of V2O5, followed by partial reduction by annealing in Ar. The resulting films are heterogeneous, consisting of various metallic/oxide phases and including regions with VO2 stoichiometry. A gradual metal insulator transition with a nearly two order of magnitude change in film resistance is observed between room temperature and 140 °C. In addition, the films exhibit a temperature coefficient of resistance of ˜ -2.4%/ °C from 20 to 140 °C.

  15. Metal-insulator transition in nanocomposite VO{sub x} films formed by anodic electrodeposition

    Energy Technology Data Exchange (ETDEWEB)

    Tsui, Lok-kun; Lu, Jiwei; Zangari, Giovanni, E-mail: gz3e@virginia.edu [Department of Materials Science and Engineering, University of Virginia, 395 McCormick Rd., Charlottesville, Virginia 22904 (United States); Hildebrand, Helga; Schmuki, Patrik [Department for Materials Science LKO, University of Erlangen-Nuremberg, Martensstr. 7, D-91058 Erlangen (Germany)

    2013-11-11

    The ability to grow VO{sub 2} films by electrochemical methods would open a low-cost, easily scalable production route to a number of electronic devices. We have synthesized VO{sub x} films by anodic electrodeposition of V{sub 2}O{sub 5}, followed by partial reduction by annealing in Ar. The resulting films are heterogeneous, consisting of various metallic/oxide phases and including regions with VO{sub 2} stoichiometry. A gradual metal insulator transition with a nearly two order of magnitude change in film resistance is observed between room temperature and 140 °C. In addition, the films exhibit a temperature coefficient of resistance of ∼ −2.4%/ °C from 20 to 140 °C.

  16. Interfacial phenomena in electric field-assisted anodic bonding of Kovar/Al film-glass

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    Anodic bonding of glass to Kovar alloy coated with Al film (Glass-Al film/Kovar) was performed in the temperature range of 513~713?K under the static electric voltage of 500?V in order to investigate the interfacial phenomena of Al-glass joint. The results reveal that Na and K ions within the glass are displaced by the applied field from the anode-side surface of the glass to form depletion layers of them. The K ion depletion layer is narrow and followed by a K pile-up layer, and both the two layers are formed within the Na depletion layer. The width of the Na and K depletion layers is increased with increasing bonding temperature and time. The activation energies for the growth of both depletion layers were close to that for Na diffusion in the glass. TEM observations reveal that Al film coated at the surface of Kovar alloy is oxidized to amorphous Al2O3 containing a few of Fe, Ni and Co by oxygen ions from the glass drifted by high electric field during bonding. The amount of Fe ions diffusing into the glass adjacent to the anode is significantly low due to the presence of Al film between Kovar alloy and the glass. As a result, the amorphous reaction layer of Fe-Si-O in the glass near the interface is avoided which is formed in Kovar-glass joints.

  17. Anodic formation of binary and ternary compound semiconductor films for photovoltaic cells

    Energy Technology Data Exchange (ETDEWEB)

    Schimmel, M.I.; Bottechia, O.L.; Wendt, H. [Technical University of Darmstadt (Germany). Institute of Chemical Technology

    1998-03-01

    By anodic oxidation of copper sheets in sulfide anion-containing electrolytes copper chalcogenide semiconductor films suitable for photovoltaic applications can be attained. Anodically chalcopyrite (Cu{sub 2}S) has been formed as pure, mechanically stable, homogeneous and adhesive polycrystalline films, consisting of well-developed large crystallites. Cu{sub 2}S coated copper sheets were produced with an area of 3 cm x 3 cm. P-n-junctions formed by evaporation of CdS onto the anodically formed Cu{sub 2}S films show an energy efficiency of 3.3%. The extension of this process to ternary systems, like copper/indium/sulfur, is likely to be possible. A mixture of Cu{sub 2}S and CuInS{sub 2} could be formed by codepositing In{sub 2}S{sub 3} together with Cu{sub 2}S. Cu{sub 2}Se-films with a thickness of up to 1 {mu}m were formed by chemical bath deposition. (author)

  18. Thin film metal-oxides

    CERN Document Server

    Ramanathan, Shriram

    2009-01-01

    Presents an account of the fundamental structure-property relations in oxide thin films. This title discusses the functional properties of thin film oxides in the context of applications in the electronics and renewable energy technologies.

  19. New roots to formation of nanostructures on glass surface through anodic oxidation of sputtered aluminum

    Directory of Open Access Journals (Sweden)

    Satoru Inoue, Song-Zhu Chu, Kenji Wada, Di Li and Hajime Haneda

    2003-01-01

    Full Text Available New processes for the preparation of nanostructure on glass surfaces have been developed through anodic oxidation of sputtered aluminum. Aluminum thin film sputtered on a tin doped indium oxide (ITO thin film on a glass surface was converted into alumina by anodic oxidation. The anodic alumina gave nanometer size pore array standing vertically on the glass surface. Kinds of acids used in the anodic oxidation changed the pore size drastically. The employment of phosphoric acid solution gave several tens nanometer size pores. Oxalic acid cases produced a few tens nanometer size pores and sulfuric acid solution provided a few nanometer size pores. The number of pores in a unit area could be changed with varying the applied voltage in the anodization and the pore sizes could be increased by phosphoric acid etching. The specimen consisting of a glass substrate with the alumina nanostructures on the surface could transmit UV and visible light. An etched specimen was dipped in a TiO2 sol solution, resulting in the impregnation of TiO2 sol into the pores of alumina layer. The TiO2 sol was heated at ~400 °C for 2 h, converting into anatase phase TiO2. The specimens possessing TiO2 film on the pore wall were transparent to the light in UV–Visible region. The electro deposition technique was applied to the introduction of Ni metal into pores, giving Ni nanorod array on the glass surface. The removal of the barrier layer alumina at the bottom of the pores was necessary to attain smooth electro deposition of Ni. The photo catalytic function of the specimens possessing TiO2 nanotube array was investigated in the decomposition of acetaldehyde gas under the irradiation of UV light, showing that the rate of the decomposition was quite large.

  20. Preparation of Porous Alumina Film on Aluminum Substrate by Anodization in Oxalic Acid

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    Self-ordering of the cell arrangement of the anodic porous alumina was prepared in oxalic acid solution at a constant potential of 40V and at a temperature of 20°C. The honeycomb structure made by one step anodization method and two step anodization method is different.Pores in the alumina film prepared by two step anodization method were more ordered than those by one step anodization method.

  1. Ordered Nanomaterials Thin Films via Supported Anodized Alumina Templates

    Directory of Open Access Journals (Sweden)

    Mohammed eES-SOUNI

    2014-10-01

    Full Text Available Supported anodized alumina template films with highly ordered porosity are best suited for fabricating large area ordered nanostructures with tunable dimensions and aspect ratios. In this paper we first discuss important issues for the generation of such templates, including required properties of the Al/Ti/Au/Ti thin film heterostructure on a substrate for high quality templates. We then show examples of anisotropic nanostructure films consisting of noble metals using these templates, discuss briefly their optical properties and their applications to molecular detection using surface enhanced Raman spectroscopy. Finally we briefly address the possibility to make nanocomposite films, exemplary shown on a plasmonic-thermochromic nanocomposite of VO2-capped Au-nanorods.

  2. TiO2 nanotube formation by Ti film anodization and their transport properties for dye-sensitized solar cells

    NARCIS (Netherlands)

    Iraj, M.; Kolahdouz, M.; Asl-Soleimani, E.; Esmaeili, E.; Kolahdouz Esfahani, Z.

    2016-01-01

    In this paper, we present the synthesis of TiO2 nanotube (NT) arrays formed by anodization of Ti film deposited on a fluorine-doped tin oxide-coated glass substrate by direct current magnetron sputtering. NH4F/ethylene glycol electrolyte was used to demonstrate the growth of stable nanotubes at room

  3. Role of aluminum doping on phase transformations in nanoporous titania anodic oxides

    Energy Technology Data Exchange (ETDEWEB)

    Bayata, Fatma [Istanbul Bilgi University, Department of Mechanical Engineering, 34060, Eyup, Istanbul (Turkey); Ürgen, Mustafa, E-mail: urgen@itu.edu.tr [Istanbul Technical University, Department of Metallurgical and Materials Engineering, 34469, Maslak, Istanbul (Turkey)

    2015-10-15

    The role of aluminium doping on anatase to rutile phase transformation of nanoporous titanium oxide films were investigated. For this purpose pure and aluminum doped metal films were deposited on alumina substrates by cathodic arc physical deposition. The nanoporous anodic oxides were prepared by porous anodizing of pure and aluminum doped titanium metallic films in an ethylene glycol + NH{sub 4}F based electrolyte. Nanoporous amorphous structures with 60–80 nm diameter and 2–4 μm length were formed on the surfaces of alumina substrates. The amorphous undoped and Al-doped TiO{sub 2} anodic oxides were heat-treated at different temperatures in the range of 280–720 °C for the investigation of their crystallization behavior. The combined effects of nanoporous structure and Al doping on crystallization behavior of titania were investigated using X-ray diffraction (XRD) and micro Raman analysis. The results indicated that both Al ions incorporated into the TiO{sub 2} structure and the nanoporous structure retarded the rutile formation. It was also revealed that presence or absence of metallic film underneath the nanopores has a major contribution to anatase-rutile transformation. - Highlights: • Al-doped TiO{sub 2} nanopores were grown on alumina substrates using anodization method. • The crystallization behavior of nanoporous Al-doped TiO{sub 2} were investigated. • Al doping into nanoporous TiO{sub 2} retarded the anatase-rutile transformation. • Nanostructuring has significant role in controlling rutile formation temperature. • The absence of the metallic film under the nanopores delayed the rutile formation.

  4. Progress in Nano-Engineered Anodic Aluminum Oxide Membrane Development

    Directory of Open Access Journals (Sweden)

    Gerrard Eddy Jai Poinern

    2011-02-01

    Full Text Available The anodization of aluminum is an electro-chemical process that changes the surface chemistry of the metal, via oxidation, to produce an anodic oxide layer. During this process a self organized, highly ordered array of cylindrical shaped pores can be produced with controllable pore diameters, periodicity and density distribution. This enables anodic aluminum oxide (AAO membranes to be used as templates in a variety of nanotechnology applications without the need for expensive lithographical techniques. This review article is an overview of the current state of research on AAO membranes and the various applications of nanotechnology that use them in the manufacture of nano-materials and devices or incorporate them into specific applications such as biological/chemical sensors, nano-electronic devices, filter membranes and medical scaffolds for tissue engineering.

  5. Decisive influence of colloidal suspension conductivity during electrophoretic impregnation of porous anodic film supported on 1050 aluminium substrate.

    Science.gov (United States)

    Fori, B; Taberna, P L; Arurault, L; Bonino, J P

    2014-01-01

    The present paper studies the influence of suspension conductivity on the electrophoretic deposition (EPD) of nanoparticles inside a porous anodic aluminium oxide film. It is shown that an increase in the suspension's conductivity enhances impregnation of the anodic film by the nanoparticles. Two mechanisms are seen to promote the migration of particles into the pores. Indeed an increase in the suspension conductivity leads on the one hand to a strengthening of the electric field in the anodic film and on the other hand to a thinning of the electric double layer on the pore walls. The results of our study confirm that colloidal suspension conductivity is a key parameter governing the electrophoretic impregnation depth.

  6. The Effect of Silane on the Microstructure, Corrosion, and Abrasion Resistances of the Anodic Films on Ti Alloy

    Science.gov (United States)

    Wang, Jinwei; Chen, Jiali

    2016-04-01

    Anodic oxide films on Ti-6Al-4V alloy are prepared using sodium hydroxide as the base electrolyte containing aminopropyl trimethoxysilane (APS) as an additive. Some APS undergo hydrolysis, adsorption, and chemical reaction with the TiO x to form Ti-O-Si bond as confirmed by ATR-FTIR and XPS spectra, and in turn their surface appearance and roughness are greatly changed with the addition of APS as observed by their SEM images. These amino anodic films possess much higher corrosive resistances since the formation of Ti-O-Si complex enhances the compactness of the anodic films and the existence of aminopropyl groups inside the pores provides additional blocking effects. Besides, their improvement in anti-abrasive capability is attributed to the toughening effect of the chemically bonded silanes and the lubrication functions from both the chemically bonded and physically absorbed silanes between the touched interfaces.

  7. Control of morphology and surface wettability of anodic niobium oxide microcones formed in hot phosphate-glycerol electrolytes

    International Nuclear Information System (INIS)

    Highlights: → Anodic niobium oxide microcones with nanofiber morphology are formed simply by anodizing. → The cone size and its tip angle are controlled by anodizing condition. → The surface shows extremely high contact angle for water after coating with a fluoroalkyl layer. - Abstract: We report the fabrication of superhydrophobic surfaces with a hierarchical morphology by self-organized anodizing process. Simply by anodizing of niobium metal in hot phosphate-glycerol electrolyte, niobium oxide microcones, consisting of highly branched oxide nanofibers, develop on the surface. The size of the microcones and their tip angles are controlled by changing the applied potential difference in anodizing and the water content in the electrolyte. Reduction of the water content increases the size of the microcones, with the nanofibers changing to nanoparticles. The size of microcones is also reduced by increasing the applied potential difference, without influencing the tip angle. The hierarchical oxide surfaces are superhydrophilic, with static contact angles close to 0o. Coating of the anodic oxide films with a monolayer of fluoroalkyl phosphate makes the surfaces superhydrophobic with a contact angle for water as high as 175o and a very small contact angle hysteresis of only 2o. The present results indicate that the larger microcones with smaller tip angles show the higher contact angle for water.

  8. Rare Earth Oxide Thin Films

    CERN Document Server

    Fanciulli, Marco

    2007-01-01

    Thin rare earth (RE) oxide films are emerging materials for microelectronic, nanoelectronic, and spintronic applications. The state-of-the-art of thin film deposition techniques as well as the structural, physical, chemical, and electrical properties of thin RE oxide films and of their interface with semiconducting substrates are discussed. The aim is to identify proper methodologies for the development of RE oxides thin films and to evaluate their effectiveness as innovative materials in different applications.

  9. Performance of laboratory polymer electrolyte membrane hydrogen generator with sputtered iridium oxide anode

    Science.gov (United States)

    Labou, D.; Slavcheva, E.; Schnakenberg, U.; Neophytides, S.

    The continuous improvement of the anode materials constitutes a major challenge for the future commercial use of polymer electrolyte membranes (PEM) electrolyzers for hydrogen production. In accordance to this direction, iridium/titanium films deposited directly on carbon substrates via magnetron sputtering are operated as electrodes for the oxygen evolution reaction interfaced with Nafion 115 electrolyte in a laboratory single cell PEM hydrogen generator. The anode with 0.2 mg cm -2 Ir catalyst loading was electrochemically activated by cycling its potential value between 0 and 1.2 V (vs. RHE). The water electrolysis cell was operated at 90 °C with current density 1 A cm -2 at 1.51 V without the ohmic contribution. The corresponding current density per mgr of Ir catalyst is 5 A mg -1. The achieved high efficiency is combined with sufficient electrode stability since the oxidation of the carbon substrate during the anodic polarization is almost negligible.

  10. Improved electrical properties of silicon-incorporated anodic niobium oxide formed on porous Nb-Si substrate

    International Nuclear Information System (INIS)

    In the present study, porous Nb-Si alloy films with isolated nano-column morphology have been successfully developed by oblique angle magnetron sputtering on to aluminum substrate with concave cell structure. The deposited films are amorphous with the 15 at% silicon supersaturated into niobium. The porous Nb-15 at% Si films, as well as niobium films with similar morphology, are anodized at several voltages up to 50 V in 0.1 mol dm-3 ammonium pentaborate electrolyte. Due to the presence of sufficient gaps between neighboring columns, the gaps are not filled with anodic oxide, despite the large Pilling-Bedworth ratio (for instance, 2.6 for Nb/Nb2O5) and hence, a linear correlation between the reciprocal of capacitance and formation voltage is obtained for the Nb-15 at% Si. From the comparison with the anodic films formed on porous niobium films, it has been found that silicon addition improves the thermal stability of anodic niobium oxide; the change in capacitance and increase in leakage current become small for the Nb-Si. The findings indicate the potential of oblique angle deposition to tailor porous non-equilibrium niobium alloy films for high performance niobium-base capacitor.

  11. Effect of Oxide Inclusions on Electrochemical Properties of Aluminium Sacrificial Anodes

    Institute of Scientific and Technical Information of China (English)

    M. Emamy; A. Keyvani; M. Mahta; J. Campbell

    2009-01-01

    Oxide films are incorporated into melts by an entrainment process, and are expected to be present in most metals, but particularly cast Al alloys. The oxides are necessarily present as folded-over double films (bifilms) that are effectively cracks. Their effect on the electrochemical behaviour of cast Al-5Zn-0.02ln sacrificial anodes was studied in 3 wt pct sodium chloride solution using the NACE efficiency evaluation. Three methods were employed to entrain progressive amounts of oxide in the alloy, including the addition of Al-Zn-ln maching chips to the charge, increasing the pouring height, and agitating the melt. The introduction of oxide bifilms in the cast alloy resulted in the deterioration of the electrochemical properties of the sacrificial anodes, such as current capacity and anode efficiency, and introduced increasing variability in these properties. The results suggest that corrosion behaviour is strongly related to the presence of bifilms suspended in the liquid alloy because bifilms provide crack paths allowing the corrodant to penetrate deeply into the metal matrix, and simultaneously provide localized galvanic cells because of the precipitation of Fe rich intermetallic compounds on their outer surfaces.

  12. Electrochemical and morphological analyses on the titanium surface modified by shot blasting and anodic oxidation processes

    International Nuclear Information System (INIS)

    In recent years, many surface modification processes have been developed in order to induce the osseointegration on titanium surface and thus to improve the implants' biocompatibility. In this work, Ti surface has been modified by shot blasting followed by anodic oxidation process in order to associate the good surface characteristics of both processes to obtain a rough and porous surface able to promote the titanium surface bioactivity. Commercially pure titanium (grade 2) plates were used on the surface treatments that were as follows: Shot blasting (SB) performed using alumina (Al2O3) particles, and anodic oxidation (AO) using NaOH electrolyte. The morphology, structural changes and the open-circuit potentials (OCP) of the surfaces were analyzed. It can be observed that an increase on the roughness of the blasted surface and a rough and porous surface happens after the AO process. The anodic film produced is thin and followed the blasted surface topography. It can be observed that there are small pores with regular shape covering the entire surface. X-ray diffraction results showed the presence of the anatase and rutile phases on the blasted and anodized surface after heat treatment at 600 °C/1 h. Concerning electrochemical measurements, when the different samples were submitted to open-circuit conditions in a physiological electrolyte, the protective effect increases with the oxidation process due to the oxide layer. When the surface was blasted, the OCP was more negative when compared with the Ti surface without surface treatments. - Highlights: ► A combination of shot blasting and anodic oxidation surface treatments is proposed. ► Both processes produced an increase in roughness compared to the polished surface. ► The combination of processes produced a rough and porous surface. ► Open circuit results show that the protective effect increases with oxidation process. ► The combination of processes presents the better results in this work

  13. Surfactant-assisted growth of anodic nanoporous niobium oxide with a grained surface

    International Nuclear Information System (INIS)

    Nanoporous niobium oxide film with a maximum thickness of 520 nm was prepared by anodizing niobium in a mixture of 1 wt% HF, 1 M H3PO4, and a small amount of Sodium Dodecyl Sulfate (SDS) surfactant. The porosity of the anodic niobium oxide prepared without SDS is irregular with the surface of the oxide suggesting a grained surface pattern rather than an ordered porous structure. A proper amount of SDS addition can prepare a pore arrangement with stripe patterns. The pore depth and surface pattern were strongly affected by the concentration of SDS and bath temperature. We found that the addition of SDS surfactant facilitated improvement in the chemical resistance of niobium oxide, leading to the formation of pores with a longer length compared to those prepared without a SDS surfactant. This can be in part ascribed to the protection of the surface by the physical adsorption of SDS on the surface due to a charge-charge interaction and be in part attributed to the formation of Nb=O bonding on the outermost oxide layer by SDS. When anodization was carried out for 4 h, the surface dissolution of niobium oxide was observed, which means that the maximum tolerance time against chemical dissolution was less than 4 h.

  14. High-performance anode-supported solid oxide fuel cell with impregnated electrodes

    Science.gov (United States)

    Osinkin, D. A.; Bogdanovich, N. M.; Beresnev, S. M.; Zhuravlev, V. D.

    2015-08-01

    The 61%NiO + 39%Zr0.84Y0.16O1.92 (NiO-YSZ) and 56%NiO + 44%Zr0.83Sc0.16Ce0.01O1.92 (NiO-CeSSZ) composite powders have been prepared using two-steps and one-step combustion synthesis, respectively. The Ni-YSZ anode substrate with a low level of electrical resistance (less than 1 mOhm cm) and porosity of about 53% in the reduced state was fabricated. The functional layer of the anode with the high level of electrochemical activity was made of NiO-CeSSZ. The single anode-supported solid oxide fuel cell with the bi-layer Ni-cermet anode, Zr0.84Sc0.16O1.92 film electrolyte and the Pt + 3% Zr0.84Y0.16O1.92 cathode was fabricated. The power density and the U-I curves of the fuel cell at initial state and after impregnation of the cathode and anode by praseodymium and cerium oxides, respectively, have been measured at different temperatures. The maximum of power density of the initial fuel cell was 0.35 W cm-2 at conditions of wet hydrogen (air) supply to the anode (cathode) at 900 °C. After the electrodes were impregnated, the value of power density increased by seven times and was approximately 2.4 W cm-2 at 0.6 V. It was suggested that after the electrodes impregnation the polarization resistance of the fuel cell was determined by the gas diffusion in the supported anode.

  15. Anodization of AZ91 magnesium alloy in alkaline solution containing silicate and corrosion properties of anodized films

    Institute of Scientific and Technical Information of China (English)

    LI Ling-ling; CHENG Ying-liang; WANG Hui-min; ZHANG Zhao

    2008-01-01

    The anodization of AZ91 magnesium alloy in an alkaline electrolyte of 100g/L NaOH+20g/L Na2B4O7·10H2O+50g/L C6H5Na3O7·2H2O+60g/L Na2SiO3·9H2O was studied.The corrosion resistance of the anodized films was studied by electrochemical impedance spectroscopy (EIS) and potentiodynamic polarization techniques.The microstructure of the films was examined with scanning electronic microscope (SEM) and X-ray diffractometer (XRD).The results show that,under the experimental conditions,the optimum anodizing time and the optimum anodizing current density are 40min and 20mA/cm2 respectively for obtaining the anodic film with high corrosion resistance.The XRD pattern shows that the components of the anodized film consist of MgO and Mg2 (SiO4).

  16. High Performance SLED Fabricated by Pulsed Anodic Oxidation

    Institute of Scientific and Technical Information of China (English)

    GAO Xin; BO Bao-xue; ZHANG Jing; LI Hui; QU Yi

    2009-01-01

    InGaAs/AlGaAs MQW superluminescent LED (SLED) is fabricated by using pulsed anodic oxidation and molecular beam epitaxy (MBE). The power and spectral output characteristics of three kinds of device structures are investigated. An output power above 10mW with FWHM of 18nm is demonstrated at a current of 150mA.

  17. A review of liquid metal anode solid oxide fuel cells

    Directory of Open Access Journals (Sweden)

    ALIYA TOLEUOVA

    2013-06-01

    Full Text Available This review discusses recent advances in a solid oxide fuel cell (SOFC variant that uses liquid metal electrodes (anodes with the advantage of greater fuel tolerance and the ability to operate on solid fuel. Key features of the approach are discussed along with the technological and research challenges that need to be overcome for scale-up and commercialisation.

  18. Spatial atomic layer deposition on flexible porous substrates: ZnO on anodic aluminum oxide films and Al{sub 2}O{sub 3} on Li ion battery electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Sharma, Kashish [Department of Chemistry and Biochemistry, University of Colorado, Boulder, Colorado 80309 (United States); Routkevitch, Dmitri; Varaksa, Natalia [InRedox, Longmont, Colorado 80544 (United States); George, Steven M., E-mail: Steven.George@Colorado.Edu [Department of Chemistry and Biochemistry, University of Colorado, Boulder, Colorado 80309 and Department of Mechanical Engineering, University of Colorado, Boulder, Colorado 80309 (United States)

    2016-01-15

    Spatial atomic layer deposition (S-ALD) was examined on flexible porous substrates utilizing a rotating cylinder reactor to perform the S-ALD. S-ALD was first explored on flexible polyethylene terephthalate polymer substrates to obtain S-ALD growth rates on flat surfaces. ZnO ALD with diethylzinc and ozone as the reactants at 50 °C was the model S-ALD system. ZnO S-ALD was then performed on nanoporous flexible anodic aluminum oxide (AAO) films. ZnO S-ALD in porous substrates depends on the pore diameter, pore aspect ratio, and reactant exposure time that define the gas transport. To evaluate these parameters, the Zn coverage profiles in the pores of the AAO films were measured using energy dispersive spectroscopy (EDS). EDS measurements were conducted for different reaction conditions and AAO pore geometries. Substrate speeds and reactant pulse durations were defined by rotating cylinder rates of 10, 100, and 200 revolutions per minute (RPM). AAO pore diameters of 10, 25, 50, and 100 nm were utilized with a pore length of 25 μm. Uniform Zn coverage profiles were obtained at 10 RPM and pore diameters of 100 nm. The Zn coverage was less uniform at higher RPM values and smaller pore diameters. These results indicate that S-ALD into porous substrates is feasible under certain reaction conditions. S-ALD was then performed on porous Li ion battery electrodes to test S-ALD on a technologically important porous substrate. Li{sub 0.20}Mn{sub 0.54}Ni{sub 0.13}Co{sub 0.13}O{sub 2} electrodes on flexible metal foil were coated with Al{sub 2}O{sub 3} using 2–5 Al{sub 2}O{sub 3} ALD cycles. The Al{sub 2}O{sub 3} ALD was performed in the S-ALD reactor at a rotating cylinder rate of 10 RPM using trimethylaluminum and ozone as the reactants at 50 °C. The capacity of the electrodes was then tested versus number of charge–discharge cycles. These measurements revealed that the Al{sub 2}O{sub 3} S-ALD coating on the electrodes enhanced the capacity stability. This S

  19. The preparation and corrosion resistance of Ce and Nd modified anodic films on aluminum

    Energy Technology Data Exchange (ETDEWEB)

    Li Qizheng; Tang Yuming [School of Materials Science and Engineering, Beijing University of Chemical Technology, Beijing 100029 (China); Zuo Yu, E-mail: zuoy@mail.buct.edu.cn [School of Materials Science and Engineering, Beijing University of Chemical Technology, Beijing 100029 (China)

    2010-04-15

    Rare earth element Ce and Nd modified anodic films were prepared on aluminum surface by a relatively simple method: the aluminum samples were first immersed in Ni(NO{sub 3}){sub 2} solutions containing Ce or Nd salts at 90 deg. C, then were dried and anodized. The contents of Ce or Nd in the anodic films were from 0.5% to 0.9%, and about 4-5% Ni was also introduced in the films. The modified anodic films were more compact with much smaller pores and increased hardness. In neutral, acidic and basic NaCl solutions, the rare earth modified films showed obviously improved corrosion resistance. The Ce modified films showed better corrosion resistance than Nd modified films. The cracking resistance of the films under heating was also improved.

  20. Anodic Aluminum Oxide Templates for Nano wires Array Fabrication

    International Nuclear Information System (INIS)

    This paper reports on the process developed to fabricate anodic aluminium oxide (AAO) templates suitable for the fabrication of nano wire arrays. Anodization process has been used to fabricate the AAO templates with pore diameters ranging from 15 nm to 30 nm. Electrodeposition of parallel arrays of high aspect ratio nickel nano wires were demonstrated using these fabricated AAO templates. The nano wires produced were characterized using X-ray diffraction (XRD) and scanning electron microscopy (SEM). It was found that the orientations of the electrodeposited nickel nano wires were governed by the deposition current and electrolyte conditions. (author)

  1. The Effects of Different Anodizing Voltages on the Nanoporous Titanium Oxide

    OpenAIRE

    DİKİİCİ, Tuncay; Toparli, Mustafa

    2014-01-01

    The purpose of this study was to invesitigate and analyze the nanoporous titanium oxide layers produced on titanium (Cp-Ti) by electrochemical anodization with different voltages (5, 10, 20, 40, 80 V). Titanium oxide (TiO2) layers were formed in a %1.5 HF solution using a dc power supply for 30 min. The effect of applied potential on the physical properties of nanoporous strucutre including pore diameter, wall thickness, interpore distance and film thickness was studied. The surface roughness...

  2. Anodes for Solid Oxide Fuel Cells Operating at Low Temperatures

    DEFF Research Database (Denmark)

    Abdul Jabbar, Mohammed Hussain

    . On the other hand, low-temperature operation poses serious challenges to the electrode performance. Effective catalysts, redox stable electrodes with improved microstructures are the prime requisite for the development of efficient SOFC anodes. The performance of Nb-doped SrT iO3 (STN) ceramic anodes......An important issue that has limited the potential of Solid Oxide Fuel Cells (SOFCs) for portable applications is its high operating temperatures (800-1000 ºC). Lowering the operating temperature of SOFCs to 400-600 ºC enable a wider material selection, reduced degradation and increased lifetime......, an investigation on the effect of application of cathodic polarization on Ni-YSZ anodes is described....

  3. Platinum thin film anodes for solid acid fuel cells

    OpenAIRE

    Louie, Mary W.; Haile, Sossina M.

    2011-01-01

    Hydrogen electro-oxidation kinetics at the Pt | CsH_2PO_4 interface have been evaluated. Thin films of nanocrystalline platinum 7.5–375 nm thick and 1–19 mm in diameter were sputtered atop polycrystalline discs of the proton-conducting electrolyte, CsH_2PO_4, by shadow-masking. The resulting Pt | CsH_2PO_4 | Pt symmetric cells were studied under uniform H_2-H_2O-Ar atmospheres at temperatures of 225–250 °C using AC impedance spectroscopy. For thick platinum films (>50 nm), electro-oxidation o...

  4. Blue luminescence in porous anodic alumina films: the role of the oxalic impurities

    CERN Document Server

    Gao Tao; Zhang Li

    2003-01-01

    Porous anodic alumina (PAA) films with ordered nanopore arrays have been prepared by electrochemically anodizing aluminium in oxalic acid solutions, and the role of the oxalic impurities in the optical properties of PAA films has been discussed. Photoluminescence (PL) measurements show that the PAA films obtained have a blue PL band with a peak position at around 470 nm; the oxalic impurities, incorporated in the PAA films during the anodization processes and already existing in them, could be being transformed into PL centres and hence responsible for this PL emission.

  5. Lateral V/VOx/V Tunnel Junctions Formed by Anodic Oxidation

    Science.gov (United States)

    Kirkwood, David; West, Kevin; Lu, Jiwei; Wolf, Stuart

    2008-03-01

    Anodization has been found to be a simple and cost effective technique to produce oxide films of many transition metals. In this work, we have used anodic oxidation as a means of fabricating lateral V/VOx/V junctions. Vanadium wires grown by ion beam deposition were patterned by lithography and an active working window was defined on the wire. VOx was then grown under galvanostatic control in a two electrode electrochemical micro-cell. A droplet of oxygen rich saturated Boric acid was used as the electrolyte to electrically connect the Vandium working electrode to a Platinum wire counter electrode. A constant current of approximately 100 μA/cm^2 was maintained through the cell for various amounts of time. Electrical measurements of the resulting V/VOx/V junctions indicate a metal to insulator transition (MIT) near 340 ^oK that is similar to the structural phase transition and accompanied MIT of VO2 which occurs at this temperature. A 4-fold change in resistance is observed in the junctions. Below this transition temperature a typical junction behavior is observed with a dramatic change in resistance state from high to low with increasing applied current. This non-linear IV characteristic on the junction with a size of 5 μm by 15 μm suggests that the anodized VOx film behaves like a tunneling barrier.

  6. Stability of the anodic growth porous tungsten oxide in different solutions

    Energy Technology Data Exchange (ETDEWEB)

    Chai, Y.; Yam, F. K.; Hassan, Z. [Nano-Optoelectronic Research and Technology Laboratory, School of Physics, Universiti Sains Malaysia, 11800 Penang (Malaysia)

    2015-05-15

    This article presents the study of the stability of the anodic growth porous tungsten oxide (WO{sub 3}) film in different solutions. As-anodized films are relatively stable in acidic electrolytes like sulphuric acid (H{sub 2}SO{sub 4}), hydrochloric acid (HCl) but not in oxalic acid. In higher pH solution, rate of dissolution of the WO{sub 3} film is higher. Annealing at 400 °C for 2 h transform the as-grown sample from amorphous phase to the crystalline phase and this significantly improve the stability of the film in high pH solution. Photocurrent measurements reveal that there is no significant difference of the electrolyte used (0.5 M H{sub 2}SO{sub 4}, 0.33 M H{sub 3}PO{sub 4}, 0.1 M sodium sulfate (Na{sub 2}SO{sub 4})) on the photocurrent. As-annealed films exhibit good stablility for the long photoelectrochemical (PEC) measurements (1700 s) in 0.5 M H{sub 2}SO{sub 4} and 0.1 M Na{sub 2}SO{sub 4}. There is no effect on the photocurrent for the variation of the concentration of the acidic solution (H{sub 2}SO{sub 4}). However, lower photocurrent was obtained as the concentration of Na{sub 2}SO{sub 4} was increased.

  7. Multi-metallic anodes for solid oxide fuel cell applications

    International Nuclear Information System (INIS)

    A new method for direct preparation of materials for solid oxide fuel cell anode - Ni- YSZ cermets - based on mechanical alloying (MA) of the original powders is developed, allowing to admix homogeneously any component. Additive metals are selected from thermodynamic criteria, leading to compacts consolidation through sintering by activated surface (SAS). The combined process MA-SSA can reduce the sintering temperature by 300 deg C, yielding porous anodes. Densification mechanisms are discussed from quasi-isothermal sintering kinetics results. Doping with Ag, W, Cu, Mo, Nb, Ta, in descending order, promotes the densification of pellets through liquid phase sintering and evaporation of metals and oxides, which allow reducing the sintering temperature. Powders and pellets characterization by electronic microscopy and X-ray diffraction completes the result analyses. (author)

  8. Exploding metal film active anode source experiments on the LION extractor ion diode

    International Nuclear Information System (INIS)

    In this paper the authors report results using an extractor geometry magnetically insulated ion diode on the 0.5 TW LION accelerator. Experiments with an exploding metal film active anode plasma source (EMFAAPS) have shown that intense beams with significantly improved turn-on time compared to epoxy-filled-groove anodes can be produced. A new geometry, in which a plasma switch is used to provide the current path that explodes the thin film anode, has improved the ion efficiency (to typically 70%) compared with the previous scheme in which an electron collector on the anode provided this current. Leakage electron current is reduced when no collector is used

  9. Alternative anode materials for solid oxide fuel cells

    Energy Technology Data Exchange (ETDEWEB)

    Goodenough, John B.; Huang, Yun-Hui [Texas Materials Institute, ETC 9.102, 1 University Station, C2200, The University of Texas at Austin, Austin, TX 78712 (United States)

    2007-11-08

    The electrolyte of a solid oxide fuel cell (SOFC) is an O{sup 2-}-ion conductor. The anode must oxidize the fuel with O{sup 2-} ions received from the electrolyte and it must deliver electrons of the fuel chemisorption reaction to a current collector. Cells operating on H{sub 2} and CO generally use a porous Ni/electrolyte cermet that supports a thin, dense electrolyte. Ni acts as both the electronic conductor and the catalyst for splitting the H{sub 2} bond; the oxidation of H{sub 2} to H{sub 2}O occurs at the Ni/electrolyte/H{sub 2} triple-phase boundary (TPB). The CO is oxidized at the oxide component of the cermet, which may be the electrolyte, yttria-stabilized zirconia, or a mixed oxide-ion/electron conductor (MIEC). The MIEC is commonly a Gd-doped ceria. The design and fabrication of these anodes are evaluated. Use of natural gas as the fuel requires another strategy, and MIECs are being explored for this application. The several constraints on these MIECs are outlined, and preliminary results of this on-going investigation are reviewed. (author)

  10. Anodic oxides on a beta type Nb-Ti alloy and their characterization by electrochemical impedance spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Woldemedhin, Michael Teka; Hassel, Achim Walter [Max Planck Institut fuer Eisenforschung GmbH, Duesseldorf (Germany); Institute for Chemical Technology of Inorganic Materials, Johannes Kepler University, Linz (Austria); Raabe, Dierk [Max Planck Institut fuer Eisenforschung GmbH, Duesseldorf (Germany)

    2010-04-15

    Anodic oxides were grown on the surface of an electropolished (Ti-30 at% Nb) beta-titanium ({beta}-Ti) alloy by cyclic voltammetry. The scan rate was 100 mV s{sup -1} between 0 and 8 V in increments of l V in an acetate buffer of pH 6.0. Electrochemical impedance spectroscopy was carried out right after each anodic oxide growth increment to study the electronic properties of the oxide/electrolyte interface in a wide frequency range from 100 kHz to 10 MHz with an AC perturbation voltage of 10 mV. A film formation factor of 2.4 nm V{sup -1} was found and a relative permittivity number (dielectric constant) of 42.4 was determined for the oxide film formed. Mott-Schottky analysis on a potentiostatically formed 7 nm thick oxide film was performed to assess the semiconducting properties of the mixed anodic oxide grown on the alloy. A flat band potential of -0.47 V (standard hydrogen electrode, SHE) was determined, connected to a donor density of 8.2 x 10{sup 17} cm{sup -3}. {beta}-Ti being highly isotropic in terms of mechanical properties should be superior to the stiffer {alpha}-Ti compound. Its application, however, requires a passivation behaviour comparable or better than {alpha}-Ti which in fact is found. (Abstract Copyright [2010], Wiley Periodicals, Inc.)

  11. Vanadium-based anode catalysts for solid oxide fuel cells

    Energy Technology Data Exchange (ETDEWEB)

    Fu, X.Z.; Luo, J.L.; Chuang, K.T.; Sanger, A.R. [Alberta Univ., Edmonton, AB (Canada). Dept. of Chemical and Materials Engineering; Tu, H.Y. [Shanghai Jiao Tong Univ., Shanghai (China). Inst. of Fuel Cell, School of Mechanical Engineering; Yang, Q.M. [Vale-Inco Ltd., Mississauga, ON (Canada)

    2010-07-01

    Solid oxide fuel cells (SOFCs) are considered as important electricity generators because they convert carbon-containing fuels from fossil sources to electricity without generating pollution. Syngas is more available and less expensive than highly purified hydrogen. However, when exposed to syngas at SOFC operating temperatures, conventional nickel anode catalysts result in carbon deposition, which compromises their performance. Syngas derived from conversion of hydrocarbon or coal resources normally also contain hydrogen sulphide, which poisons nickel anode catalysts. In order to use syngas, it is necessary to either stringently clean the feed, which is a costly process, or develop catalysts that can operate using impure feed and are not prone to carbon deposition. This paper discussed the development of a vanadium-based material (VOx) which is an active anode catalyst for SOFCs, that is not prone to coking and is sulfur resistant. The VOx material was obtained by decomposition and reduction of ammonium metavanadate (NH{sub 4}VO{sub 3}) at high temperature. Coking and sulfur resistance of as-prepared VOx and nickel were compared in hydrogen sulphide-containing syngas environments at 900 degrees Celsius. It was concluded that the VOx material had much higher coking resistance and sulfur tolerance than nickel. The SOFC with VOx anode catalyst demonstrated excellent performance using hydrogen sulphide-containing syngas as fuel. 3 refs.

  12. A Stability Study of Ni/Yttria-Stabilized Zirconia Anode for Direct Ammonia Solid Oxide Fuel Cells.

    Science.gov (United States)

    Yang, Jun; Molouk, Ahmed Fathi Salem; Okanishi, Takeou; Muroyama, Hiroki; Matsui, Toshiaki; Eguchi, Koichi

    2015-12-30

    In recent years, solid oxide fuel cells fueled with ammonia have been attracting intensive attention. In this work, ammonia fuel was supplied to the Ni/yttria-stabilized zirconia (YSZ) cermet anode at 600 and 700 °C, and the change of electrochemical performance and microstructure under the open-circuit state was studied in detail. The influence of ammonia exposure on the microstructure of Ni was also investigated by using Ni/YSZ powder and Ni film deposited on a YSZ disk. The obtained results demonstrated that Ni in the cermet anode was partially nitrided under an ammonia atmosphere, which considerably roughened the Ni surface. Moreover, the destruction of the anode support layer was confirmed for the anode-supported cell upon the temperature cycling test between 600 and 700 °C because of the nitriding phenomenon of Ni, resulting in severe performance degradation.

  13. Influence of ethanol content in the precursor solution on anodic electrodeposited CeO2 thin films

    International Nuclear Information System (INIS)

    Ceria thin films have been anodically deposited onto 316L stainless steel in bath solutions containing different volume ratios of ethanol (0, 10, 40, 70 and 100% v/v). The influence of ethanol content on the electroplating behavior, and the structural and corrosion properties of the cerium oxide films were studied with electrochemical impedance spectroscopy, scanning electron microscopy, ellipsometry, X-ray diffraction, and Raman and X-ray photoelectron spectroscopy. Results show that ethanol content plays a significant role on the properties of the deposited ceria films but negligible effect on their electroplating behavior. The as-deposited films are mostly in the Ce(IV) oxidation state and the stoichiometry is around CeO1.90 for all samples. With the increase of ethanol content from 0 to 100% v/v, the average grain diameter and film thickness of the obtained ceria film decrease from 16.8 nm to 11.1 nm and from 32.9 nm to 15.8 nm, respectively. Using a deposition bath solution containing 10% v/v ethanol, a layer of compacted yellowish gold ceria film with the minimum porosity of 19.9%, mean crystalline diameter of 15.4 nm, and maximum corrosion resistance of 3.31 × 10−5 Ω has been obtained. - Highlights: • Ethanol plays a negligible effect on ceria film anodic electroplating behavior. • Average grain diameter and thickness of the film decrease with the ethanol addition. • Appropriate amount of ethanol can markedly improve the film quality. • Film color changes gradually with increasing ethanol addition into deposition bath. • Nanocrystalline CeO1.90 films of golden yellowish have been obtained

  14. Effect of film thickness on electrochromic activity of spray deposited iridium oxide thin films

    International Nuclear Information System (INIS)

    Electrochromic iridium oxide thin films were deposited onto fluorine doped tin oxide (FTO) coated glass substrates from an aqueous iridium chloride solution using a spray pyrolysis process. The deposition temperature was 250 deg. C. The solution quantity was varied from 25 to 55 ml to obtain films with different thickness. The as-deposited samples were X-ray amorphous. The electrochromic properties were studied in proton containing electrolyte (0.5N, H2SO4) using cyclic voltammetry, chronoamperometry and spectrophotometry techniques. The films exhibit anodic electrochromism. The colouration efficiency at 630 nm was maximum for thicker sample, owing to its large charge storage capacity and hydration

  15. Effect of film thickness on electrochromic activity of spray deposited iridium oxide thin films

    Energy Technology Data Exchange (ETDEWEB)

    Patil, P.S. [Thin Film Materials Laboratory, Department of Physics, Shivaji University, Kolhapur 416004 (India)]. E-mail: psp_phy@unishivaji.ac.in; Mujawar, S.H. [Thin Film Materials Laboratory, Department of Physics, Shivaji University, Kolhapur 416004 (India); Sadale, S.B. [Thin Film Materials Laboratory, Department of Physics, Shivaji University, Kolhapur 416004 (India); Deshmukh, H.P. [Department of Physics, Bharati Vidyapeeth, Deemed University, Y.M. College, Pune (India); Inamdar, A.I. [Thin Film Materials Laboratory, Department of Physics, Shivaji University, Kolhapur 416004 (India)

    2006-10-10

    Electrochromic iridium oxide thin films were deposited onto fluorine doped tin oxide (FTO) coated glass substrates from an aqueous iridium chloride solution using a spray pyrolysis process. The deposition temperature was 250 deg. C. The solution quantity was varied from 25 to 55 ml to obtain films with different thickness. The as-deposited samples were X-ray amorphous. The electrochromic properties were studied in proton containing electrolyte (0.5N, H{sub 2}SO{sub 4}) using cyclic voltammetry, chronoamperometry and spectrophotometry techniques. The films exhibit anodic electrochromism. The colouration efficiency at 630 nm was maximum for thicker sample, owing to its large charge storage capacity and hydration.

  16. Anodized Nanoporous Titania Thin Films for Dental Application: Structure’ Effect on Corrosion Behavior

    Directory of Open Access Journals (Sweden)

    A. Boucheham

    2016-06-01

    Full Text Available Nanostructured Titania layers formed on the surface of titanium and titanium alloys by anodic oxidation play an important role in the enhancement of their biocompatibility and osseointegration in the human body. For this purpose, we aimed to study in the current work the structural and electrochemical properties of amorphous and crystallized nanostructured TiO2 thin films elaborated on Ti6Al4V substrate by electrochemical anodization in fluoride ions (F– containing electrolyte at 10 V during 15 min and heat treated in air at 550 °C for 2 h. The morphology, chemical composition and phase composition of synthesized layers were investigated using field emission scanning electron microscopy (FE-SEM and X-ray diffraction (XRD. The corrosion resistance improvement of both as-anodized and annealed titania layers was evaluated in 0.9 wt. % NaCl solution with pH = 6.4 at room temperature by means of open circuit potential (Eoc,potentiodynamic polarization (PDYN and electrochemical impedance spectroscopy (EIS.

  17. Porous anodic film formation on an Al-3.5 wt % Cu alloy

    Directory of Open Access Journals (Sweden)

    Páez, M. A.

    2003-12-01

    Full Text Available The morphological development of porous anodic films in the initial stages is examined during anodizing an Al-3.5 wt % Cu alloy in phosphoric acid. Using transmission electron microscopy a sequence of ultramicrotomed anodic sections reveals the dynamic evolution of numerous features in the thickening film in the initial stages of anodizing. The morphological changes in the anodic oxide in the initial stages of its formation appears related to the formation of bubbles during film growth. From Rutherford backscattering spectroscopy (RBS analysis of the film, the formation of the bubbles is associated with the enrichment of copper in the alloy due to growth of the anodic oxide. On the other hand, during constant current anodizing of Al-Cu in phosphoric acid, the current efficiency is considerably less than that for anodizing superpure aluminium under similar conditions. From the contrasting results between the charge consumed calculated from RBS and the real charge consumed during anodizing, oxygen gas bubbles generation and copper oxidation seem to be of less importance on the low efficiency for film formation. It is apparent that the main cause of losing efficiency for film growth on Al-Cu is associated with generation of oxygen at residual second phase, with the development of stresses in the film and, the consequence of these effects on film cracking during film growth.

    En este trabajo se examinó el desarrollo morfológico de películas anódicas porosas en los estados iniciales de la anodización de una aleación de aluminio Al-3,5 % p/p Cu. La observación de una secuencia de secciones ultramicrotomadas del metal y su película anódica, por microscopía electrónica de transmisión, revela la evolución dinámica de numerosos detalles morfológicos durante los inicios del crecimiento de la película anódica. Los cambios morfológicos en el óxido anódico, en los inicios de su formación, aparecen relacionados a la formación de

  18. SnO2-graphene nanocomposite free-standing film as anode in lithium-ion batteries

    Science.gov (United States)

    Choi, Eunmi; Kim, Daeun; Lee, Ilbok; Chae, Su Jin; Kim, Areum; Pyo, Sung Gyu; Yoon, Songhun

    2015-09-01

    SnO2-reduced graphene oxide nanocomposite in the form of a free-standing film was prepared by simple chemical synthesis. The homogeneous and compact formation of the nanocomposite of SnO2 and reduced graphene oxide was confirmed by various analysis methods. When incorporated as anode in lithium-ion batteries, a high capacity (503 mAh g-1) and very stable cycle life were observed. These favorable properties probably arise from the efficient relaxation of high mechanical stress by the reduced graphene-oxide layers during the lithiation-delithiation process within SnO2. [Figure not available: see fulltext.

  19. INFLUENCE OF MAGNETIC FIELD ON ACCURACY OF ECM BY CHANGING THE CONDUCTIVITY OF ANODE FILM

    Institute of Scientific and Technical Information of China (English)

    FAN Zhijian; ZHANG Lixin; TANG lin

    2008-01-01

    The change of conductivity, thickness and scanning electron microscopy (SEM) appearance of the anode film of CrWMn in 10( NaNO3 at different anode potential either with or without the magnetic field applied are investigated by testing film resistance, galvanostatic transient and using SEM to design magnetic circuit in magnetic assisted electrochemical machining (MAECM). The experiments show that the anode film has semi-conducting property. Compared with the situation without magnetic field applied, the resistance of the film formed at 1.8V (anode potential) increased and decreased at 4.0V while B=0.4T and the magnetic north pole points toward anode. The SEM photo demonstrates that the magnetic field will densify the film in the passivation area and quicken dissolution of the anode metal in over-passivation area. Based on the influence of magnetic field on electrochemical machining(ECM) due to the changes of the anode film conductivity behavior, the magnetic north pole should be designed to point towards the workpiece surface that has been machined. Process experiments agree with the results of test analysis.

  20. Hydrogenated amorphous silicon thin film anode for proton conducting batteries

    Science.gov (United States)

    Meng, Tiejun; Young, Kwo; Beglau, David; Yan, Shuli; Zeng, Peng; Cheng, Mark Ming-Cheng

    2016-01-01

    Hydrogenated amorphous Si (a-Si:H) thin films deposited by chemical vapor deposition were used as anode in a non-conventional nickel metal hydride battery using a proton-conducting ionic liquid based non-aqueous electrolyte instead of alkaline solution for the first time, which showed a high specific discharge capacity of 1418 mAh g-1 for the 38th cycle and retained 707 mAh g-1 after 500 cycles. A maximum discharge capacity of 3635 mAh g-1 was obtained at a lower discharge rate, 510 mA g-1. This electrochemical discharge capacity is equivalent to about 3.8 hydrogen atoms stored in each silicon atom. Cyclic voltammogram showed an improved stability 300 mV below the hydrogen evolution potential. Both Raman spectroscopy and Fourier transform infrared spectroscopy studies showed no difference to the pre-existing covalent Si-H bond after electrochemical cycling and charging, indicating a non-covalent nature of the Si-H bonding contributing to the reversible hydrogen storage of the current material. Another a-Si:H thin film was prepared by an rf-sputtering deposition followed by an ex-situ hydrogenation, which showed a discharge capacity of 2377 mAh g-1.

  1. Structured SiCu thin films in LiB as anodes

    International Nuclear Information System (INIS)

    Both helical and inclined columnar Si–10 at.% Cu structured thin films were deposited on Cu substrates using glancing angle deposition (GLAD) technique. In order to deposit Cu and Si two evaporation sources were used. Ion assistance was utilized in the first 5 min of the GLAD to enhance the adhesion and the density of the films. These films were characterized by thin film XRD, GDOES, SEM, and EDS. Electrochemical characterizations were made by testing the thin films as anodes in half-cells for 100 cycles. The results showed that the columnar SiCu thin film delivered 2200 mAh g−1, where the helical one exhibited 2600 mAh g−1, and, their initial coulombic efficiencies were found to be 38%–50% respectively. For the columnar and the helical thin film anodes, sustainable 520 and 800 mAh g−1 with 90% and 99% coulombic efficiencies were achieved for 100 cycles. These sustainable capacities showed the importance of the thin film structure having nano-sized crystals and amorphous particles. The higher surface area of the helices increases the capacity of the electrode because the contact area of the thin film anode with Li ions is increased, and the polarization which otherwise forms on the anode surface due to SEI formation is decreased. In addition, because of larger interspaces between the helices the ability of the anode to accommodate the volumetric changes is improved, which results in a higher coulombic efficiency and capacity retention during cycling test. - Highlights: • Cu and Si atoms were co-evaporated to form composite thin film. • GLAD is an alternative method to form new electrodes for LIB. • Uses of the composite helices and nanocolumns as anodes were shown experimentally. • IAD was used to improve the adhesion of the structured thin films. • High surface area, porosities and Cu presence improve the Si anode performance

  2. Unidirectional oxide hetero-interface thin-film diode

    International Nuclear Information System (INIS)

    The unidirectional thin-film diode based on oxide hetero-interface, which is well compatible with conventional thin-film fabrication process, is presented. With the metal anode/electron-transporting oxide (ETO)/electron-injecting oxide (EIO)/metal cathode structure, it exhibits that electrical currents ohmically flow at the ETO/EIO hetero-interfaces for only positive voltages showing current density (J)-rectifying ratio of ∼105 at 5 V. The electrical properties (ex, current levels, and working device yields) of the thin-film diode (TFD) are systematically controlled by changing oxide layer thickness. Moreover, we show that the oxide hetero-interface TFD clearly rectifies an AC input within frequency (f) range of 102 Hz < f < 106 Hz, providing a high feasibility for practical applications

  3. Unidirectional oxide hetero-interface thin-film diode

    Science.gov (United States)

    Park, Youngmin; Lee, Eungkyu; Lee, Jinwon; Lim, Keon-Hee; Kim, Youn Sang

    2015-10-01

    The unidirectional thin-film diode based on oxide hetero-interface, which is well compatible with conventional thin-film fabrication process, is presented. With the metal anode/electron-transporting oxide (ETO)/electron-injecting oxide (EIO)/metal cathode structure, it exhibits that electrical currents ohmically flow at the ETO/EIO hetero-interfaces for only positive voltages showing current density (J)-rectifying ratio of ˜105 at 5 V. The electrical properties (ex, current levels, and working device yields) of the thin-film diode (TFD) are systematically controlled by changing oxide layer thickness. Moreover, we show that the oxide hetero-interface TFD clearly rectifies an AC input within frequency (f) range of 102 Hz < f < 106 Hz, providing a high feasibility for practical applications.

  4. Unidirectional oxide hetero-interface thin-film diode

    Energy Technology Data Exchange (ETDEWEB)

    Park, Youngmin; Lee, Eungkyu; Lee, Jinwon; Lim, Keon-Hee [Program in Nano Science and Technology, Graduate School of Convergence Science and Technology, Seoul National University, Seoul 151-742 (Korea, Republic of); Kim, Youn Sang, E-mail: younskim@snu.ac.kr [Program in Nano Science and Technology, Graduate School of Convergence Science and Technology, Seoul National University, Seoul 151-742 (Korea, Republic of); Advanced Institute of Convergence Technology, Gyeonggi-do 443-270 (Korea, Republic of)

    2015-10-05

    The unidirectional thin-film diode based on oxide hetero-interface, which is well compatible with conventional thin-film fabrication process, is presented. With the metal anode/electron-transporting oxide (ETO)/electron-injecting oxide (EIO)/metal cathode structure, it exhibits that electrical currents ohmically flow at the ETO/EIO hetero-interfaces for only positive voltages showing current density (J)-rectifying ratio of ∼10{sup 5} at 5 V. The electrical properties (ex, current levels, and working device yields) of the thin-film diode (TFD) are systematically controlled by changing oxide layer thickness. Moreover, we show that the oxide hetero-interface TFD clearly rectifies an AC input within frequency (f) range of 10{sup 2} Hz < f < 10{sup 6} Hz, providing a high feasibility for practical applications.

  5. Aluminum/MoO3 anode thin films: an effective anode structure for highperformance flexible organic optoelectronics

    Institute of Scientific and Technical Information of China (English)

    Ding Lei; Zhang Fanghui; Ma Ying; Zhang Maili

    2012-01-01

    We report Al/MoO3 thin film used as a complex anode in high-performance OLEDs.The unique efficacy of the device was found to result from the enhanced injection of holes into the commonly used hole-transporting molecules due to a large reduction in the interface dipole at the anode/organic interface.The superior optical characteristics are attributed to a strong cavity effect,Due to the ease of processing Al/MoO3 we successfully demonstrated large-area flexible OLEDs on plastic substrates with uniform emission.

  6. Removal of organic contaminants from secondary effluent by anodic oxidation with a boron-doped diamond anode as tertiary treatment

    Energy Technology Data Exchange (ETDEWEB)

    Garcia-Segura, Sergi, E-mail: sergigarcia@ub.edu [Advanced Water Management Centre, The University of Queensland, Level 4, Gehrmann Bld. (60), St Lucia, QLD 072 (Australia); Laboratori d’Electroquímica dels Materials i del Medi Ambient, Departament de Química Física, Facultat de Química, Universitat de Barcelona, Martí i Franquès 1-11, 08028 Barcelona (Spain); Keller, Jürg [Advanced Water Management Centre, The University of Queensland, Level 4, Gehrmann Bld. (60), St Lucia, QLD 072 (Australia); Brillas, Enric [Laboratori d’Electroquímica dels Materials i del Medi Ambient, Departament de Química Física, Facultat de Química, Universitat de Barcelona, Martí i Franquès 1-11, 08028 Barcelona (Spain); Radjenovic, Jelena, E-mail: j.radjenovic@awmc.uq.edu.au [Advanced Water Management Centre, The University of Queensland, Level 4, Gehrmann Bld. (60), St Lucia, QLD 072 (Australia)

    2015-02-11

    Graphical abstract: - Highlights: • Mineralization of secondary effluent by anodic oxidation with BDD anode. • Complete removal of 29 pharmaceuticals and pesticides at trace level concentrations. • Organochlorine and organobromine byproducts were formed at low μM concentrations. • Chlorine species evolution assessed to evaluate the anodic oxidation applicability. - Abstract: Electrochemical advanced oxidation processes (EAOPs) have been widely investigated as promising technologies to remove trace organic contaminants from water, but have rarely been used for the treatment of real waste streams. Anodic oxidation with a boron-doped diamond (BDD) anode was applied for the treatment of secondary effluent from a municipal sewage treatment plant containing 29 target pharmaceuticals and pesticides. The effectiveness of the treatment was assessed from the contaminants decay, dissolved organic carbon and chemical oxygen demand removal. The effect of applied current and pH was evaluated. Almost complete mineralization of effluent organic matter and trace contaminants can be obtained by this EAOP primarily due to the action of hydroxyl radicals formed at the BDD surface. The oxidation of Cl{sup −} ions present in the wastewater at the BDD anode gave rise to active chlorine species (Cl{sub 2}/HClO/ClO{sup −}), which are competitive oxidizing agents yielding chloramines and organohalogen byproducts, quantified as adsorbable organic halogen. However, further anodic oxidation of HClO/ClO{sup −} species led to the production of ClO{sub 3}{sup −} and ClO{sub 4}{sup −} ions. The formation of these species hampers the application as a single-stage tertiary treatment, but posterior cathodic reduction of chlorate and perchlorate species may reduce the risks associated to their presence in the environment.

  7. Removal of organic contaminants from secondary effluent by anodic oxidation with a boron-doped diamond anode as tertiary treatment

    International Nuclear Information System (INIS)

    Graphical abstract: - Highlights: • Mineralization of secondary effluent by anodic oxidation with BDD anode. • Complete removal of 29 pharmaceuticals and pesticides at trace level concentrations. • Organochlorine and organobromine byproducts were formed at low μM concentrations. • Chlorine species evolution assessed to evaluate the anodic oxidation applicability. - Abstract: Electrochemical advanced oxidation processes (EAOPs) have been widely investigated as promising technologies to remove trace organic contaminants from water, but have rarely been used for the treatment of real waste streams. Anodic oxidation with a boron-doped diamond (BDD) anode was applied for the treatment of secondary effluent from a municipal sewage treatment plant containing 29 target pharmaceuticals and pesticides. The effectiveness of the treatment was assessed from the contaminants decay, dissolved organic carbon and chemical oxygen demand removal. The effect of applied current and pH was evaluated. Almost complete mineralization of effluent organic matter and trace contaminants can be obtained by this EAOP primarily due to the action of hydroxyl radicals formed at the BDD surface. The oxidation of Cl− ions present in the wastewater at the BDD anode gave rise to active chlorine species (Cl2/HClO/ClO−), which are competitive oxidizing agents yielding chloramines and organohalogen byproducts, quantified as adsorbable organic halogen. However, further anodic oxidation of HClO/ClO− species led to the production of ClO3− and ClO4− ions. The formation of these species hampers the application as a single-stage tertiary treatment, but posterior cathodic reduction of chlorate and perchlorate species may reduce the risks associated to their presence in the environment

  8. Surface Morphology and Growth of Anodic Titania Nanotubes Films: Photoelectrochemical Water Splitting Studies

    Directory of Open Access Journals (Sweden)

    Chin Wei Lai

    2015-01-01

    become the most studied material as they exhibit promising functional properties. In the present study, anodic TiO2 films with different surface morphologies can be synthesized in an organic electrolyte of ethylene glycol (EG by controlling an optimum content of ammonium fluoride (NH4F using electrochemical anodization technique. Based on the results obtained, well-aligned and bundle-free TiO2 nanotube arrays with diameter of 100 nm and length of 8 µm were successfully synthesized in EG electrolyte containing ≈5 wt% of NH4F for 1 h at 60 V. However, formation of nanoporous structure and compact oxide layer would be favored if the content of NH4F was less than 5 wt%. In the photoelectrochemical (PEC water splitting studies, well-aligned TiO2 nanotubular structure exhibited higher photocurrent density of ≈1 mA/cm2 with photoconversion efficiency of ≈2% as compared to the nanoporous and compact oxide layer due to the higher active surface area for the photon absorption to generate more photo-induced electrons during photoexcitation stage.

  9. Mechanical properties of anodic titanium films containing ions of Ca and P submitted to heat and hydrothermal treatment.

    Science.gov (United States)

    de Lima, Gabriel G; de Souza, Gelson B; Lepienski, Carlos M; Kuromoto, Neide K

    2016-12-01

    Anodic oxidation is a technique widely used to improve the bioactivity of Ti surface. In this study, micro-arc oxidation (MAO) was used to obtain an anodic film incorporating Ca and P ions to evaluate the effect of heat and hydrothermal treatment on the mechanical and in vitro bioactivity properties of these new layers. The MAO process was carried out using (CH3COO)2Ca·H2O and NaH2PO4·2H2O electrolytes under galvanostatic mode (150mA/cm(2)). The thermal treatments were made at 400°C and 600°C in air atmosphere while hydrothermal treatment was made in an alkaline water solution at 130°C. These surfaces presented desired mechanical properties for biomedical applications owing to the rutile and anatase phases in the anodic film that are more crystalline after thermal treatments; which provided an increase in hardness values and lower elastic modulus. The dry sliding wear resistance increased by performing thermal treatments on the surfaces with one condition still maintaining the film after the test. Bioactivity was investigated by immersion in simulated body fluid during 21 days and hydroxyapatite was formed on all samples. Finally, lower values of contact angle were obtained for heat treated samples. PMID:27479891

  10. Electrochemical degradation of clofibric acid in water by anodic oxidation

    Energy Technology Data Exchange (ETDEWEB)

    Sires, Ignasi [Laboratori de Ciencia i Tecnologia Electroquimica de Materials, Departament de Quimica Fisica, Facultat de Quimica, Universitat de Barcelona, Marti i Franques 1-11, 08028 Barcelona (Spain); Cabot, Pere Lluis [Laboratori de Ciencia i Tecnologia Electroquimica de Materials, Departament de Quimica Fisica, Facultat de Quimica, Universitat de Barcelona, Marti i Franques 1-11, 08028 Barcelona (Spain); Centellas, Francesc [Laboratori de Ciencia i Tecnologia Electroquimica de Materials, Departament de Quimica Fisica, Facultat de Quimica, Universitat de Barcelona, Marti i Franques 1-11, 08028 Barcelona (Spain); Garrido, Jose Antonio [Laboratori de Ciencia i Tecnologia Electroquimica de Materials, Departament de Quimica Fisica, Facultat de Quimica, Universitat de Barcelona, Marti i Franques 1-11, 08028 Barcelona (Spain); Rodriguez, Rosa Maria [Laboratori de Ciencia i Tecnologia Electroquimica de Materials, Departament de Quimica Fisica, Facultat de Quimica, Universitat de Barcelona, Marti i Franques 1-11, 08028 Barcelona (Spain); Arias, Conchita [Laboratori de Ciencia i Tecnologia Electroquimica de Materials, Departament de Quimica Fisica, Facultat de Quimica, Universitat de Barcelona, Marti i Franques 1-11, 08028 Barcelona (Spain); Brillas, Enric [Laboratori de Ciencia i Tecnologia Electroquimica de Materials, Departament de Quimica Fisica, Facultat de Quimica, Universitat de Barcelona, Marti i Franques 1-11, 08028 Barcelona (Spain)]. E-mail: brillas@ub.edu

    2006-10-05

    Aqueous solutions containing the metabolite clofibric acid (2-(4-chlorophenoxy)-2-methylpropionic acid) up to close to saturation in the pH range 2.0-12.0 have been degraded by anodic oxidation with Pt and boron-doped diamond (BDD) as anodes. The use of BDD leads to total mineralization in all media due to the efficient production of oxidant hydroxyl radical ({center_dot}OH). This procedure is then viable for the treatment of wastewaters containing this compound. The effect of pH, apparent current density, temperature and metabolite concentration on the degradation rate, consumed specific charge and mineralization current efficiency has been investigated. Comparative treatment with Pt yields poor decontamination with complete release of stable chloride ion. When BDD is used, this ion is oxidized to Cl{sub 2}. Clofibric acid is more rapidly destroyed on Pt than on BDD, indicating that it is more strongly adsorbed on the Pt surface enhancing its reaction with {center_dot}OH. Its decay kinetics always follows a pseudo-first-order reaction and the rate constant for each anode increases with increasing apparent current density, being practically independent of pH and metabolite concentration. Aromatic products such as 4-chlorophenol, 4-chlorocatechol, 4-chlororesorcinol, hydroquinone, p-benzoquinone and 1,2,4-benzenetriol are detected by gas chromatography-mass spectrometry (GC-MS) and reversed-phase chromatography. Tartronic, maleic, fumaric, formic, 2-hydroxyisobutyric, pyruvic and oxalic acids are identified as generated carboxylic acids by ion-exclusion chromatography. These acids remain stable in solution using Pt, but they are completely converted into CO{sub 2} with BDD. A reaction pathway for clofibric acid degradation involving all these intermediates is proposed.

  11. The key factor determining the anodic deposition of vanadium oxides

    International Nuclear Information System (INIS)

    This work demonstrates that anodic deposition of vanadium oxide (denoted as VOx.nH2O) can be considered as the chemical co-precipitation of V5+ and V4+ oxy-/hydroxyl species and the accumulation of V5+ species at the vicinity of electrode surface is the key factor for the successful anodic deposition of VOx.nH2O at a potential much more negative than the equilibrium potential of the oxygen evolution reaction (OER). The results of in situ UV-vis spectra show that the V4+/V5+ ratio near the electrode surface can be controlled by varying the applied potential, leading to different, three-dimensional (3D) nanostructures of VOx.nH2O. The accumulation of V5+ species due to V4+ oxidation at potentials ≥0.4 V (vs. Ag/AgCl) has been found to be very similar to the phenomenon by adding H2O2 in the deposition solution. The X-ray photoelectron spectroscopic (XPS) results show that all VOx.nH2O deposits can be considered as aggregates consisting of mixed V5+ and V4+ oxy-/hydroxyl species with the mean oxidation state significantly increasing with the applied electrode potential.

  12. Composite anodes based on nanotube titanium oxide from electro-oxidation of Ti metal substrate

    Science.gov (United States)

    Pozio, A.; Carewska, M.; Mura, F.; D'Amato, R.; Falconieri, M.; De Francesco, M.; Appetecchi, G. B.

    2014-02-01

    In this manuscript is reported an investigation on lithium-ion battery composite anodes based on nanotube titanium oxide active material obtained from electrochemical oxidation of titanium metal substrates. Nanotube TiO2 showed a good nominal capacity, particularly taking into account that no electronic conductive additive as well as no binder was incorporated into the TiO2 material. The performance of nanotube titanium oxide anode tapes was compared with that of electrodes based on TiO2 both commercially available and obtained from laser pyrolysis. Cycling tests have indicated that the anodes based on electrosynthesized nanotube TiO2 exhibit the best performance in terms of capacity values and rate capability in combination with very good capacity retention and coulombic efficiency leveling 100% even at high rates.

  13. Fabrication of TiO2 Crystalline Coatings by Combining Ti-6Al-4V Anodic Oxidation and Heat Treatments

    Directory of Open Access Journals (Sweden)

    María Laura Vera

    2015-01-01

    Full Text Available The bio- and hemocompatibility of titanium alloys are due to the formation of a TiO2 layer. This natural oxide may have fissures which are detrimental to its properties. Anodic oxidation is used to obtain thicker films. By means of this technique, at low voltages oxidation, amorphous and low roughness coatings are obtained, while, above a certain voltage, crystalline and porous coatings are obtained. According to the literature, the crystalline phases of TiO2, anatase, and rutile would present greater biocompatibility than the amorphous phase. On the other hand, for hemocompatible applications, smooth and homogeneous surfaces are required. One way to obtain crystalline and homogeneous coatings is by heat treatments after anodic oxidation. The aim of this study is to evaluate the influence of heat treatments on the thickness, morphology, and crystalline structure of the TiO2 anodic coatings. The characterization was performed by optical and scanning electron microscopy, X-ray diffraction, and X-ray reflectometry. Coatings with different colors of interference were obtained. There were no significant changes in the surface morphology and roughness after heat treatment of 500°C. Heat treated coatings have different proportions of the crystalline phases, depending on the voltage of anodic oxidation and the temperature of the heat treatment.

  14. Tracer studies of anodic films formed on aluminium in malonic and oxalic acids

    Energy Technology Data Exchange (ETDEWEB)

    Garcia-Vergara, S.J. [Corrosion and Protection Centre, School of Materials, The University of Manchester, P.O. Box 88, Manchester M60 1QD (United Kingdom)], E-mail: s.garcia-vergara@manchester.ac.uk; Skeldon, P.; Thompson, G.E. [Corrosion and Protection Centre, School of Materials, The University of Manchester, P.O. Box 88, Manchester M60 1QD (United Kingdom); Habakaki, H. [Graduate School of Engineering, Hokkaido University, N13-W8, Sapporo 060-8628 (Japan)

    2007-12-30

    Using a tungsten-containing layer, incorporated into sputtering-deposited aluminium, as a tracer, the growth of porous anodic films in malonic and oxalic acid electrolytes has been investigated using transmission electron microscopy, Rutherford backscattering spectroscopy and nuclear reaction analysis. Comparisons were also made with films formed in phosphoric acid electrolyte, which have been studied previously. The findings reveal a distortion of the tracer layer within the barrier region of the porous films, evident as a lagging of the tracer beneath the pores relative to that in the adjacent cell wall region. Further, the films are significantly thicker than the layer of metal consumed during anodizing and display smooth-sided pores. The anodizing behaviours are consistent with a major role for field-assisted flow of film material within the barrier layer in the development of the pores.

  15. Science Letters:Anodic oxidation of salicylic acid at Ta/BDD electrode

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    Boron-doped diamond (BDD) film electrodes using Ta as substrates were employed for anodic oxidation of salicylic acid (SA). The effects of operational variables including initial concentration, current density, temperature and pH were examined.The results showed that BDD films deposited on the Ta substrates had high electrocatalytic activity for SA degradation. There was little effect of pH on SA degradation. The current efficiency (CE) was found to be dependent mainly on the initial SA concentration,current density and temperature. Chemical oxygen demand (COD) was reduced from 830 mg/L to 42 mg/L under a current density of 200 A/m2 at 30 ℃.

  16. Solid oxide fuel cell power plant with an anode recycle loop turbocharger

    Energy Technology Data Exchange (ETDEWEB)

    Saito, Kazuo; Skiba, Tommy; Patel, Kirtikumar H.

    2016-09-27

    An anode exhaust recycle turbocharger (100) has a turbocharger turbine (102) secured in fluid communication with a compressed oxidant stream within an oxidant inlet line (218) downstream from a compressed oxidant supply (104), and the anode exhaust recycle turbocharger (100) also includes a turbocharger compressor (106) mechanically linked to the turbocharger turbine (102) and secured in fluid communication with a flow of anode exhaust passing through an anode exhaust recycle loop (238) of the solid oxide fuel cell power plant (200). All or a portion of compressed oxidant within an oxidant inlet line (218) drives the turbocharger turbine (102) to thereby compress the anode exhaust stream in the recycle loop (238). A high-temperature, automotive-type turbocharger (100) replaces a recycle loop blower-compressor (52).

  17. Solid oxide fuel cell power plant with an anode recycle loop turbocharger

    Science.gov (United States)

    Saito, Kazuo; Skiba, Tommy; Patel, Kirtikumar H.

    2015-07-14

    An anode exhaust recycle turbocharger (100) has a turbocharger turbine (102) secured in fluid communication with a compressed oxidant stream within an oxidant inlet line (218) downstream from a compressed oxidant supply (104), and the anode exhaust recycle turbocharger (100) also includes a turbocharger compressor (106) mechanically linked to the turbocharger turbine (102) and secured in fluid communication with a flow of anode exhaust passing through an anode exhaust recycle loop (238) of the solid oxide fuel cell power plant (200). All or a portion of compressed oxidant within an oxidant inlet line (218) drives the turbocharger turbine (102) to thereby compress the anode exhaust stream in the recycle loop (238). A high-temperature, automotive-type turbocharger (100) replaces a recycle loop blower-compressor (52).

  18. Fabrication and optical properties of platinum nanowire arrays on anodic aluminium oxide templates

    Institute of Scientific and Technical Information of China (English)

    高铁仁; 陈子瑜; 彭勇; 李发伸

    2002-01-01

    Arrays of Pt nanowires, fabricated by electrodepositing Pt metal into nanoporous anodic aluminium oxide (AAO)templates, exhibit a preferable optical absorption band in the ultraviolet-visible (UV-VIS) spectra and present a blueshift as the wire aspect ratio increases or its radius decreases. This type of optical property of Pt nanowire/porous alumina composites has been theoretically explored using Maxwell-Garnett (MG) effective medium theory. The MG theory,however, is only applicable to nanowires with an infinitesimally small radius relative to the wavelength of an incident light. The nanowire radius is controlled by the pore radius of the host alumina, which depends on anodizing conditions such as the selected electrolyte, anodizing time, temperature and voltage. The nanowire aspect ratios depend on the amount of Pt deposited into the nanopores of AAO films. The optical absorption properties of the arrays of Pt nanowires with diameters of 24, 55 and 90nm have been investigated by the UV-VIS spectra, which show that the extinction maximum (λmax) shifts to shorter wavelength side as the wire aspect ratio increases or its radius decreases.The results are qualitatively consistent with those calculated based on the MG theory.

  19. Luminescence of oxide films during the electrolytic oxidation of tantalum

    International Nuclear Information System (INIS)

    Highlights: • Electrolytic oxidation of tantalum in phosphoric acid and oxalic acid. • Galvanoluminescence (GL) is related to the existence of flaws in oxide coating. • GL is more intense for higher current density and higher electrolyte temperature. • GL shows wide bands mostly in the visible and near infrared spectral region. • Spectrum under spark discharging reveals only oxygen and hydrogen lines. - Abstract: Luminescence during a constant current electrolytic oxidation of tantalum in phosphoric acid and oxalic acid is investigated. Weak anodic luminescence (galvanoluminescence) of barrier oxide films during the electrolytic oxidation is correlated to the existence of surface imperfections. Galvanoluminescence is more intense for rougher tantalum samples, higher current density, and higher electrolyte temperature. Spectral characterization of galvanoluminescence showed that there are wide luminescence bands mostly in the visible and near infrared spectral region. Small sized sparks generated by dielectric breakdown cause rapidly increasing luminescence intensity. The luminescence spectrum under spark discharging has several intensive peaks caused by electronic transitions in oxygen and hydrogen atoms

  20. OXIDATION OF DRY HYDROCARBONS AT HIGH-POWER DENSITY ANODES

    Energy Technology Data Exchange (ETDEWEB)

    K.Krist; O. Spaldon-Stewart; R. Remick

    2004-03-01

    This work builds upon discoveries by the University of Pennsylvania and others pertaining to the oxidation of dry hydrocarbon fuels in high temperature solid oxide fuel cells. The work reported here was restricted primarily to dry methane and confirms that YSZ-based cells, having ceria in the anode as a catalyst and copper in the anode as a current collector, can operate on dry methane for extended periods. Thirty-three lab-scale cells of various designs were fabricated and operated under a variety of conditions. The longest-lived cell gave stable performance on dry methane at 800 C for over 305 hours. Only slight carbon deposition was noted at the completion of the test. A corresponding nickel/YSZ-based anode would have lasted for less than an hour under these test conditions (which included open circuit potential measurements) before carbon fouling essentially destroyed the cell. The best performing cell achieved 112 mW/cm{sub 2} on dry methane at 800 C. Several problems were encountered with carbon fouling and declining open circuit voltages in many of the test cells after switching from operation on hydrogen to dry methane. Although not rigorously confirmed by experimentation, the results suggested that air infiltration through less than perfect perimeter seals or pinholes in the electrolytes, or both gave rise to conditions that caused the carbon fouling and OCV decline. Small amounts of air reacting with methane in a partial oxidation reaction could produce carbon monoxide that, in turn, would deposit the carbon. If this mechanism is confirmed, it implies that near perfect hardware is required for extended operation. Some evidence was also found for the formation of electrical shorts, probably from carbon deposits bridging the electrolyte. Work with odorized methane and with methane containing 100-ppm hydrogen sulfide confirmed that copper is stable at 800 C in dry hydrocarbon fuels in the presence of sulfur. In a number of cases, but not exclusively, the

  1. AFM based anodic oxidation and its application to oxidative cutting and welding of CNT

    Institute of Scientific and Technical Information of China (English)

    2009-01-01

    Probe anodic oxidation by atomic force microscope (AFM) is one of the most important techniques in fabricating nano structures and devices. The technique was further studied in this paper. By analyzing the distribution of the electric field on substrate surface the dependence of oxide characters on field was discussed. The impacts of various parameters on oxide fabrication were experimentally studied. Based on these studies, we realized the oxidative cutting and welding of carbon nanotube (CNT) by the AFM based oxidation technique and provided a novel technique for the assembly and fabrication of CNT based nano devices.

  2. Solution processed nickel oxide anodes for organic photovoltaic devices

    Energy Technology Data Exchange (ETDEWEB)

    Mustafa, Bestoon; Griffin, Jonathan; Alsulami, Abdullah S.; Lidzey, David G.; Buckley, Alastair R., E-mail: alastair.buckley@sheffield.ac.uk [Department of Physics and Astronomy, Hicks Building, Hounsfield Road, University of Sheffield, Sheffield S3 7RH (United Kingdom)

    2014-02-10

    Nickel oxide thin films have been prepared from a nickel acetylacetonate (Ni(acac)) precursor for use in bulk heterojunction organic photovoltaic devices. The conversion of Ni(acac) to NiO{sub x} has been investigated. Oxygen plasma treatment of the NiO layer after annealing at 400 °C affords solar cell efficiencies of 5.2%. Photoelectron spectroscopy shows that high temperature annealing converts the Ni(acac) to a reduced form of nickel oxide. Additional oxygen plasma treatment further oxidizes the surface layers and deepens the NiO work function from 4.7 eV for the annealed film, to 5.0 eV allowing for efficient hole extraction at the organic interface.

  3. Fabrication of Sn-Ni alloy film anode for Li-ion batteries by electrochemical deposition

    Institute of Scientific and Technical Information of China (English)

    ZHANG Da-wei; YANG Chen-ge; DAI Jun; WEN Jian-wu; WANG Long; CHEN Chun-hua

    2009-01-01

    Sn-Ni alloy films for Li-ion batteries were fabricated by electrochemical deposition with rough copper foils as current collectors.The influence of electrochemical-deposition temperature and heat treatment were also investigated.By galvanostatic cell cycling the film anodes can deliver a steady specific capacity.The morphological changes cause the differences in capacity retention.After farther heat treatment,the film anodes present a better cycle performance,with a specific capacity of 314 mA-h/g after 100 cycles.This high capacity retention can be due to its smooth,compact surface formed in the heat treatment process.

  4. Characterization and Tribological Properties of Hard Anodized and Micro Arc Oxidized 5754 Quality Aluminum Alloy

    Directory of Open Access Journals (Sweden)

    M. Ovundur

    2015-03-01

    Full Text Available This study was initiated to compare the tribological performances of a 5754 quality aluminum alloy after hard anodic oxidation and micro arc oxidation processes. The structural analyses of the coatings were performed using XRD and SEM techniques. The hardness of the coatings was determined using a Vickers micro-indentation tester. Tribological performances of the hard anodized and micro arc oxidized samples were compared on a reciprocating wear tester under dry sliding conditions. The dry sliding wear tests showed that the wear resistance of the oxide coating generated by micro arc oxidation is remarkably higher than that of the hard anodized alloy.

  5. Effect of various de-anodizing techniques on the surface stability of non-colored and colored nanoporous AAO films in acidic solution

    Science.gov (United States)

    Awad, Ahmed M.; Shehata, Omnia S.; Heakal, Fakiha El-Taib

    2015-12-01

    Anodic aluminum oxide (AAO) is well known as an important nanostructured material, and a useful template in the fabrication of nanostructures. Nanoporous anodic alumina (PAA) with high open porosity was prepared by adopting three de-anodizing regimes following the first anodizing step and preceding the second one. The de-anodizing methods include electrolytic etching (EE) and chemical etching using either phosphoric acid (PE) or sodium hydroxide (HE) solutions. Three of the obtained AAO samples were black colored by electrodeposition of copper nanoparticles in their pores. Electrochemical impedance spectroscopy (EIS) and potentiodynamic polarization techniques were used to characterize the electrochemical performance of the two sets of the prepared samples. In general, the data obtained in aggressive aerated 0.5 M HCl solution demonstrated dissimilar behavior for the three prepared samples despite that the second anodizing step was the same for all of them. The data indicated that the resistance and thickness of the inner barrier part of nano-PAA film, are the main controlling factors determining its stability. On the other hand, coloring the film decreased its stability due to the galvanic effect. The difference in the electrochemical behavior of the three colored samples was discussed based on the difference in both the pore size and thickness of the outer porous part of PAA film as supported by SEM, TEM and cross-sectional micrographs. These results can thus contribute for better engineering applications of nanoporous AAO.

  6. Functionalizing Aluminum Oxide by Ag Dendrite Deposition at the Anode during Simultaneous Electrochemical Oxidation of Al.

    Science.gov (United States)

    Rafailović, Lidija D; Gammer, Christoph; Rentenberger, Christian; Trišović, Tomislav; Kleber, Christoph; Karnthaler, Hans Peter

    2015-11-01

    A novel synthesis strategy is presented for depositing metallic Ag at the anode during simultaneous electrochemical oxidation of Al. This unexpected result is achieved based on galvanic coupling. Metallic dendritic nanostructures well-anchored in a high surface area supporting matrix are envisioned to open up a new avenue of applications. PMID:26398487

  7. Anode materials for sour natural gas solid oxide fuel cells

    Science.gov (United States)

    Danilovic, Nemanja

    Novel anode catalysts have been developed for sour natural gas solid oxide fuel cell (SOFC) applications. Sour natural gas comprises light hydrocarbons, and typically also contains H2S. An alternative fuel SOFC that operates directly on sour natural gas would reduce the overall cost of plant construction and operation for fuel cell power generation. The anode for such a fuel cell must have good catalytic and electrocatalytic activity for hydrocarbon conversion, sulfur-tolerance, resistance to coking, and good electronic and ionic conductivity. The catalytic activity and stability of ABO3 (A= La, Ce and/or Sr, B=Cr and one or more of Ti, V, Cr, Fe, Mn, or Co) perovskites as SOFC anode materials depends on both A and B, and are modified by substituents. The materials have been prepared by both solid state and wet-chemical methods. The physical and chemical characteristics of the materials have been fully characterized using electron microscopy, XRD, calorimetry, dilatometry, particle size and area, using XPS and TGA-DSC-MS. Electrochemical performance was determined using potentiodynamic and potentiostatic cell testing, electrochemical impedance analysis, and conductivity measurements. Neither Ce0.9Sr0.1VO3 nor Ce0.9 Sr0.1Cr0.5V0.5O3 was an active anode for oxidation of H2 and CH4 fuels. However, active catalysts comprising Ce0:9Sr0:1V(O,S)3 and Ce0.9Sr 0.1Cr0.5V0.5(O,S)3 were formed when small concentrations of H2S were present in the fuels. The oxysulfides formed in-situ were very active for conversion of H2S. The maximum performance improved from 50 mW cm-2 to 85 mW cm -2 in 0.5% H2S/CH4 at 850°C with partial substitution of V by Cr in Ce0.9Sr0.1V(O,S)3. Selective conversion of H2S offers potential for sweetening of sour gas without affecting the hydrocarbons. Perovskites La0.75Sr0.25Cr0.5X 0.5O3--delta, (henceforth referred to as LSCX, X=Ti, Mn, Fe, Co) are active for conversion of H2, CH4 and 0.5% H2S/CH4. The order of activity in the different fuels depends on

  8. Repassivation behavior of 316L stainless steel in borate buffer solution: Kinetics analysis of anodic dissolution and film formation

    Science.gov (United States)

    Xu, Haisong; Sun, Dongbai; Yu, Hongying

    2015-12-01

    The repassivation behavior of metals or alloys after oxide film damage determines the development of local corrosion and corrosion resistance. In this work, the repassivation kinetics of 316L stainless steel (316L SS) are investigated in borate buffer solution (pH 9.1) by using the abrading electrode technique. The current densities flowing from bare 316L SS surface are measured by potentiostatic method and analyzed to characterize repassivation kinetics. The initial stages of current decay (t Avrami kinetics. Then the two independent components are analyzed individually. The film formation rate and the thickness of film are compared in different applied potential. It is shown that anodic dissolution dominates the repassivation for a short time during the early times, and a higher applied potential will promote the anodic dissolution of metal. The film growth rate increases slightly with increasing in potential. Correspondingly, increase in applied potential from 0 VSCE to 0.8 VSCE results in thicker monolayer, which covers the whole bare surface at the time of θ = 1. The electric field strengths through the thin passive film could reach 3.97 × 106 V cm-1.

  9. Metal-induced crystallization of highly corrugated silicon thick films as potential anodes for Li-ion batteries.

    Science.gov (United States)

    Qu, Fei; Li, Chilin; Wang, Zumin; Strunk, Horst P; Maier, Joachim

    2014-06-11

    Silicon has turned into one of the most promising anodes for high energy rechargeable Li-ion batteries. However, a huge volume expansion during alloying with Li always induces serious pulverization/delamination for microsized electrodes as well as undesired accumulation of solid electrolyte interphase (SEI). Many efforts have focused on various nanoengineering and binding strategies to construct integrated, robust ionic/electronic wiring networks but with a trade-off between active/inactive material ratio and performance retention. Here, we first apply a metal-induced crystallization (AIC) principle for immiscible metal/semiconductor systems (Si/Al bilayers in this work) to prepare microthick Si films consisting of a high density of isolated nanocolumns. This method furthermore brings about low temperature crystallization of initial amorphous Si and conformal coating of ion-conductive oxide to enhance the Li transport kinetics of bulk and interface. Both highly satisfactory capacity retention (1650 mAh/g after 500 cycles) and rate performance (∼1000 mAh/g at 8C) are achieved for such thick Si film anodes. This methodology can be used to prepare thick film samples with well-defined nanostructures but free of extra binder and conductive additives. It enables much higher area specific capacity than for inactive-component contained slurry samples and thin film samples. This postdeposition pore-creating can be extended to more alloying or conversion electrodes of thick films for high capacity Li/Na ion batteries. PMID:24797020

  10. Electrode Reaction Pathway in Oxide Anode for Solid Oxide Fuel Cells

    Science.gov (United States)

    Li, Wenyuan

    Oxide anodes for solid oxide fuel cells (SOFC) with the advantage of fuel flexibility, resistance to coarsening, small chemical expansion and etc. have been attracting increasing interest. Good performance has been reported with a few of perovskite structure anodes, such as (LaSr)(CrMn)O3. However, more improvements need to be made before meeting the application requirement. Understanding the oxidation mechanism is crucial for a directed optimization, but it is still on the early stage of investigation. In this study, reaction mechanism of oxide anodes is investigated on doped YCrO 3 with H2 fuel, in terms of the origin of electrochemical activity, rate-determining steps (RDS), extension of reactive zone, and the impact from overpotential under service condition to those properties. H2 oxidation on the YCs anodes is found to be limited by charge transfer and H surface diffusion. A model is presented to describe the elementary steps in H2 oxidation. From the reaction order results, it is suggested that any models without taking H into the charge transfer step are invalid. The nature of B site element determines the H2 oxidation kinetics primarily. Ni displays better adsorption ability than Co. However, H adsorption ability of such oxide anode is inferior to that of Ni metal anode. In addition, the charge transfer step is directly associated with the activity of electrons in the anode; therefore it can be significantly promoted by enhancement of the electron activity. It is found that A site Ca doping improves the polarization resistance about 10 times, by increasing the activity of electrons to promote the charge transfer process. For the active area in the oxide anode, besides the traditional three-phase boundary (3PB), the internal anode surface as two-phase boundary (2PB) is proven to be capable of catalytically oxidizing the H2 fuel also when the bulk lattice is activated depending on the B site elements. The contribution from each part is estimated by switching

  11. Preparation and Characterization of Anode-Supported YSZ Thin Film Electrolyte by Co-Tape Casting and Co-Sintering Process

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Q L; Fu, C J; Chan, S H [School of Mechanical and Aerospace Engineering, Nanyang Technological University (Singapore); Pasciak, G, E-mail: qlliu@ntu.edu.s [Electrotechnical Institute Division of Electrotechnology and Materials Science (Poland)

    2011-06-15

    In this study, a co-tape casting and co-sintering process has been developed to prepare yttria-stabilized zirconia (YSZ) electrolyte films supported on Ni-YSZ anode substrates in order to substantially reduce the fabrication cost of solid oxide fuel cells (SOFC). Through proper control of the process, the anode/electrolyte bilayer structures with a size of 7.8cm x 7.8cm were achieved with good flatness. Scanning electron microscopy (SEM) observation indicated that the YSZ electrolyte film was about 16 {mu}m in thickness, highly dense, crack free and well-bonded to the anode support. The electrochemical properties of the prepared anode-supported electrolyte film was evaluated in a button cell mode incorporating a (LaSr)MnO{sub 3}-YSZ composite cathode. With humidified hydrogen as the fuel and stationary air as the oxidant, the cell demonstrated an open-circuit voltage of 1.081 V and a maximum power density of 1.01 W/cm{sup 2} at 800 deg. C. The obtained results represent the important progress in the development of anode-supported intermediate temperature SOFC with reduced fabrication cost.

  12. Fabrication of YBCO nanowires with anodic aluminum oxide (AAO) template

    Energy Technology Data Exchange (ETDEWEB)

    Dadras, Sedigheh, E-mail: dadras@alzahra.ac.ir; Aawani, Elaheh

    2015-10-15

    We have fabricated YBCO nanowires by using anodic aluminum oxide (AAO) template and sol–gel method, to investigate the fundamental properties of the one-dimensional nanostructure YBCO high-temperature superconductor and enhance its applications. The field-emission scanning electron microscopy and X-ray diffraction pattern results have shown forming of Y-123 nanowires in the template. As an outcome, the YBCO nanowires, prepared by dipping AAO template into YBCO sol method, have average diameter of about 38 nm and length of 1 μm; this is an optimum nanowire sample with larger diameter and length. The resistance–temperature measurement indicates that the onset critical temperature of these samples occurs at 91 K, and the resistance of the optimum sample at onset transition is 10 times lower than the other sample.

  13. Studies of an extractor geometry magnetically insulated ion diode with an exploding metal film anode plasma

    International Nuclear Information System (INIS)

    Magnetically insulated diodes (MIDs) are of interest as ion sources for inertial confinement fusion. The authors examined several issues that are of concern with MIDs, including ion turn-on delay and anode plasma production, and diode impedance history and particle current scaling with the applied magnetic field and gas spacing. The LION pulsed power generator (1.5 MV, 4 Ω, 40 ns pulse length) was used to power an extractor geometry magnetically insulated (radical magnetic field) ion beam diode. The diode was studied with three anode configurations. In the first, with epoxy-filled-groove (epoxy) anodes, scaling of the ion and electron currents with the gap and the magnetic field was examined. He found that the observed ion current is consistent with a diode model that has been successful with barrel geometry MIDs. The electron leakage current scaled proportionally to 1/Bd2, where d is the anode-cathode gap spacing and B is the magnetic field strength. Studies of ion beam propagation in vacuum showed that space charge non-neutrality near the magnetic field coils caused the beam to expand initially. Later in the ion pulse (20 to 30 ns), the beam expansion became much less severe. The second anode configuration utilized an electron collector protruding above an epoxy anode surface. With the collector, he observed less bremsstrahlung across the active anode region. The last anode configuration studied was the exploding metal film active anode plasma source (EMFAAPS). Current from the accelerator was directed by an electron collector or a plasma opening switch through a thin aluminum film, which exploded to form the anode plasma

  14. Investigation of top-emitting OLEDs using molybdenum oxide as anode buffer layer

    Institute of Scientific and Technical Information of China (English)

    LIN Hui; YU Jun-sheng; ZHANG Wei

    2012-01-01

    A high-effective bottom anode is essential for high-performance top-emitting organic light-emitting devices (OLEDs).In this paper,Ag-based top-emitting OLEDs are investigated.Ag has the highest reflectivity for visible light among all metals,yet its hole-injection properties are not ideal for anodes of top-emitting OLED.The performance of the devices is significantly improved using the molybdenum oxide as anode buffer layer at the surface of Ag.By introducing the molybdenum oxide,the hole injection from Ag anodes into top-emitting OLED is largely enhanced with rather high reflectivity retained.

  15. Lithium cobalt oxide thin film and its electrochromism

    Science.gov (United States)

    Wei, Guang; Haas, Terry E.; Goldner, Ronald B.

    1989-06-01

    Thin films of lithium cobalt oxide have been prepared by RF-sputtering from powdered LiCoO2. These films permit reversible electrolytic removal of lithium ions upon application of an anodic voltage in a propylene carbonate-lithium perchlorate electrolyte, the films changing in color from a pale amber transparent state to a dark brown. A polycrystalline columnar film structure was revealed with SEM and TEM. X ray examination of the films suggests that the layered rhombohedral LiCoO2 structure is the major crystalline phase present. Oxidation-reduction titration and atomic absorption were used for the determination of the film stoichiometry. The results show that the as deposited-films on glass slides are lithium deficient (relative to the starting material) and show a high average cobalt oxidation state near +3.5. The measurements of dc conductivity suggest a band to band conduction at high temperature (300 to 430 K) and hopping conduction in localized states at low temperature (4 to 270 K). The thermoelectric power data show that the films behave as p-type semiconductors. Transmission and reflectance measurements from 400 nm to 2500 nm show significant near-IR reflectivity.

  16. Macrokinetic relationships between anodic processes in chlorine electrolysis on ruthenium-titanium oxide anodes

    International Nuclear Information System (INIS)

    Effect of porosity on kinetics of the main (chlorine evolution) and side (oxygen evolution and anodic dissolution of ruthenium dioxide) reactions for chlorine electrolysis conditions has been analyzed. Making allowance for chlorine hydrolysis secondary reaction, the distribution of chlorine concentration, solution pH and current densities of the main and side processes over the porous anode depth, have been found. It is shown that solution acidification in the anode pores due to chlorine hydrolysis can bring about replacement of oxygen evolution and ruthenium dioxide dissolution side reactions toward the porous anode external sides thus affecting its selectivity and corrosion resistance

  17. Fundamental problems with conducting oxides used as anodes

    International Nuclear Information System (INIS)

    Some problems encountered with conducting oxides when used for oxygen and chlorine anodic evolution are outlined and discussed. Also described are the classes of oxides under investigation, their applications and the immediate interests in relation to the technological demands; the preparation procedure is reviewed with emphasis on the more significant parameters for the surface characterization. These include BET surface area, morphology, chemical composition, conductivity, response to pH, point of zero charge, proton exchange ability, electrochemical 'spectrum' and electrochemical active surface area. Examples are given for RuO2, IrO2, NiCo2O4 and Co3O4. The electrocatalytic activity is also discussed by illustrating the effect of morphology and porosity, the anomalies in the determination of the reaction orders, the retarding effect of acidity in Cl2 evolution, the misleading Tafel slope due to diffusion of products with active electrodes. A review on the present understanding of the factors determining the effect of the nature of the oxides on the electrocatalytic activity is then made. (C.L.B.)

  18. Passivation of surface states by ALD-grown TiO2 overlayers on Ta3N5 anodes for photoelectrochemical water oxidation.

    Science.gov (United States)

    Zhang, Peng; Wang, Tuo; Gong, Jinlong

    2016-07-01

    This paper describes the fabrication of TiO2 overlayers by atomic layer deposition to passivate the surface states on Ta3N5 thin film anodes for photoelectrochemical water oxidation. The removal of surface states reduces the overpotential and decreases the density of surface recombination centers, resulting in enhanced activity through effective utilization of photogenerated charge carriers. PMID:27292872

  19. Characterizations of photoconductivity of graphene oxide thin films

    Directory of Open Access Journals (Sweden)

    Shiang-Kuo Chang-Jian

    2012-06-01

    Full Text Available Characterizations of photoresponse of a graphene oxide (GO thin film to a near infrared laser light were studied. Results showed the photocurrent in the GO thin film was cathodic, always flowing in an opposite direction to the initial current generated by the preset bias voltage that shows a fundamental discrepancy from the photocurrent in the reduced graphene oxide thin film. Light illumination on the GO thin film thus results in more free electrons that offset the initial current. By examining GO thin films reduced at different temperatures, the critical temperature for reversing the photocurrent from cathodic to anodic was found around 187°C. The dynamic photoresponse for the GO thin film was further characterized through the response time constants within the laser on and off durations, denoted as τon and τoff, respectively. τon for the GO thin film was comparable to the other carbon-based thin films such as carbon nanotubes and graphenes. τoff was, however, much larger than that of the other's. This discrepancy was attributable to the retardation of exciton recombination rate thanks to the existing oxygen functional groups and defects in the GO thin films.

  20. Synthesis and tribological properties of diamond-like carbon films by electrochemical anode deposition

    Science.gov (United States)

    Li, Yang; Zhang, GuiFeng; Hou, XiaoDuo; Deng, DeWei

    2012-06-01

    Diamond-like carbon films (DLC) are deposited on Ti substrate by electrochemical anodic deposition at room temperature in pure methanol solution using a pulsed DC voltage at a range from 200 V to 2000 V. Raman spectroscopy analysis of the films reveals two broaden characteristic absorption peaks centred at ˜1350 cm-1 and 1580 cm-1, relating to D- and G-band of typical DLC films, respectively. A broad peak centred at 1325-1330 cm-1 is observed when an applied potential is 1200 V, which can confirm that the deposited films contained diamond structure phase. Tribological properties of the coated Ti substrates have been measured by means of a ball-on-plate wear test machine. A related growth mechanism of DLC films by the anodic deposition mode has also been discussed.

  1. Direct methanol utilization in intermediate temperature liquid-tin anode solid oxide fuel cells

    International Nuclear Information System (INIS)

    Highlights: • Modification of Sn-based anode with Cu/SDC improves power density. • Cu and SDC improve wetting of Sn on YSZ and reduce anode polarization resistance. • Carbon formation has not been observed in SOFCs containing tin-based anodes. • Micro-channel structure in the anode reduces gas conversion resistance. - Abstract: Direct utilization of methanol in liquid tin anode solid oxide fuel cells has been experimentally demonstrated at 1023 K. A Cu and SDC modified Sn anode solid oxide fuel cell had a maximum power density of 259.2 mW/cm2 during operation on methanol. Carbon deposition was not observed in the Raman spectra of the post-test anodes. Electrochemical impedance spectroscopy indicated that gas conversion resistance increased when using methanol instead of hydrogen. The micro-channel architecture of the electrode mitigated the increase. Scanning electron microscopy images showed that addition of Cu and Sn improved wetting of Sn on YSZ and reduced anode polarization resistance. The anode gases were analyzed by mass spectroscopy and a mechanism for electrochemical oxidation of methanol has been proposed

  2. Influence of Nano-Al2O3 Powder on Micro-arc Anodic Oxidation Film of Magnesium Alloy%Al2O3纳米粉体对镁合金微弧氧化陶瓷膜性能的影响

    Institute of Scientific and Technical Information of China (English)

    包晗; 邵忠财; 刘鹏

    2013-01-01

    Nano-Al2O3 powder are added into magnesium alloy during melting process,then the prepared composite material are treated by micro-arc oxidation; also the magnesium alloy are treated by micro-arc oxidation with nano-Al2O3 powder in the electrolyte.Scanning electron microscope (SEM),X-ray diffraction (XRD) and electrochemical tests are used to analyze the influence of nano-Al2O3 powder on micro-arc anodic oxidation film.Results show that both of the two methods of adding Al2O3 powder can improve the corrosion resistance of magnesium alloy micro-arc oxidation ceramic film,but the first one is better.%在熔炼镁合金过程中加入Al2O3纳米粉体的复合材料进行微弧氧化处理;在微弧氧化电解液中加入Al2O3粉体并对镁合金基体进行微弧氧化.采用扫描电镜、X-射线衍射和电化学测试分析Al2O3粉体对镁合金微弧氧化膜层耐蚀性的影响.结果表明,两种方式加入Al2O3粉体都会提高镁合金微弧氧化陶瓷膜的耐蚀性,而熔炼过程中加入效果更佳.

  3. Fabrication of independent nickel microstructures with anodizing of aluminum,laser irradiation, and electrodeposition

    Institute of Scientific and Technical Information of China (English)

    T. Kikuchi; M. Sakairi; H. Takahashi

    2003-01-01

    Independent microstructures made of Ni metal were fabricated by five sequential processes: porous anodic oxide film for-mation, pore sealing, laser irradiation, Ni electroplating, and removal of the aluminum substrate and anodic oxide films. Aluminumplates and rods were anodized in an oxalic acid solution to form porous type anodic oxide films, and then immersed in boiling dis-tilled water for pore sealing. The anodized and pore-sealed specimens were irradiated with a pulsed neodymium-doped yttrium alu-minum garnet (Nd-YAG) laser beam in a Ni plating solution to remove anodic oxide film locally by rotating and moving up / downwith an XYZθ-stage. Nickel was deposited at the area where film had been removed by cathodic polarization in the solution beforeremoving the aluminum substrate and anodic oxide films in NaOH solutions. Cylindrical or plain network structures were fabricated successfully.

  4. Characterization of anodic SiO{sub 2} films on P-type 4H-SiC

    Energy Technology Data Exchange (ETDEWEB)

    Woon, W.S.; Hutagalung, S.D. [Electronic Materials Research Group, School of Materials and Mineral Resources Engineering, Universiti Sains Malaysia, 14300 Nibong Tebal, Penang (Malaysia); Cheong, K.Y. [Electronic Materials Research Group, School of Materials and Mineral Resources Engineering, Universiti Sains Malaysia, 14300 Nibong Tebal, Penang (Malaysia)], E-mail: cheong@eng.usm.my

    2009-02-27

    The physical and electronic properties of 100-120-nm thick anodic silicon dioxide film grown on p-type 4H-SiC wafer and annealed at different temperatures (500, 600, 700, and 800 deg. C ) have been investigated and reported. Chemical bonding of the films has been analyzed by Fourier transform infra red spectroscopy. Smooth and defect-free film surface has been revealed under field emission scanning electron microscope. Atomic force microscope has been used to study topography and surface roughness of the films. Electronic properties of the film have been investigated by high frequency capacitance-voltage and current-voltage measurements. As the annealing temperature increased, refractive index, dielectric constant, film density, SiC surface roughness, effective oxide charge, and leakage current density have been reduced until 700 deg. C . An increment of these parameters has been observed after this temperature. However, a reversed trend has been demonstrated in porosity of the film and barrier height between conduction band edge of SiO{sub 2} and SiC.

  5. Lithium alloys and metal oxides as high-capacity anode materials for lithium-ion batteries

    International Nuclear Information System (INIS)

    Highlights: •Progress in lithium alloys and metal oxides as anode materials for lithium-ion batteries is reviewed. •Electrochemical characteristics and lithium storage mechanisms of lithium alloys and metal oxides are summarized. •Strategies for improving electrochemical lithium storage properties of lithium alloys and metal oxides are discussed. •Challenges in developing lithium alloys and metal oxides as commercial anodes for lithium-ion batteries are pointed out. -- Abstract: Lithium alloys and metal oxides have been widely recognized as the next-generation anode materials for lithium-ion batteries with high energy density and high power density. A variety of lithium alloys and metal oxides have been explored as alternatives to the commercial carbonaceous anodes. The electrochemical characteristics of silicon, tin, tin oxide, iron oxides, cobalt oxides, copper oxides, and so on are systematically summarized. In this review, it is not the scope to retrace the overall studies, but rather to highlight the electrochemical performances, the lithium storage mechanism and the strategies in improving the electrochemical properties of lithium alloys and metal oxides. The challenges and new directions in developing lithium alloys and metal oxides as commercial anodes for the next-generation lithium-ion batteries are also discussed

  6. Nickel/Yttria-stabilised zirconia cermet anodes for solid oxide fuel cells

    NARCIS (Netherlands)

    Primdahl, Søren

    1999-01-01

    This thesis deals with the porous Ni/yttria-stabilized zirconia (YSZ) cermet anode on a YSZ electrolyte for solid oxide fuel cells (SOFC). Such anodes are predominantly operated in moist hydrogen at 700°C to 1000°C, and the most important technological parameters are the polarization resistance and

  7. Microstructure and optical appearance of anodized friction stir processed Al - Metal oxide surface composites

    DEFF Research Database (Denmark)

    Gudla, Visweswara Chakravarthy; Jensen, Flemming; Bordo, Kirill;

    2014-01-01

    Multiple-pass friction stir processing (FSP) was employed to impregnate Ti, Y and Ce oxide powders into the surface of an Aluminium alloy. The FSP processed surface composite was subsequently anodized with an aim to develop optical effects in the anodized layer owing to the presence of incorporated...

  8. Ni modified ceramic anodes for direct-methane solid oxide fuel cells

    Science.gov (United States)

    Xiao, Guoliang; Chen, Fanglin

    2016-01-19

    In accordance with certain embodiments of the present disclosure, a method for fabricating a solid oxide fuel cell is described. The method includes synthesizing a composition having a perovskite present therein. The method further includes applying the composition on an electrolyte support to form an anode and applying Ni to the composition on the anode.

  9. Friction stir processed Al - Metal oxide surface composites: Anodization and optical appearance

    DEFF Research Database (Denmark)

    Gudla, Visweswara Chakravarthy; Jensen, Flemming; Canulescu, Stela;

    2014-01-01

    Multiple-pass friction stir processing (FSP) was employed to impregnate metal oxide (TiO2, Y2O3 and CeO2) particles into the surface of an Aluminium alloy. The surface composites were then anodized in a sulphuric acid electrolyte. The effect of anodizing parameters on the resulting optical...

  10. Electrodeposition of Fe₃O₄ Thin Film and Its Application as Anode for Lithium Ion Batteries.

    Science.gov (United States)

    Zhao, Chongchong; Ma, Ying; Shen, Cai; Han, Weiqiang

    2016-01-01

    Fe₃O₄ films were prepared by electrodeposition under varying preparation conditions (current density, temperature, and time). The electrodeposited Fe₃O₄ were characterized in terms of morphology and composition using scanning electron microscopy (SEM) and X-ray diffraction (XRD). The electrodeposited films were also tested as anode in coin cell systems. Fluoroethylene carbonate (FEC) electrolyte was found to improve the battery performance due to formation of a better solid electrolyte interface (SEI). Conducting polymer of polypyrrole (PPY) was coated on the surface of Fe₃O₄ films for the first time with the aim to improve the electric conductivity and to buffer volume expansion of Fe₃O₄ films. PMID:27398552

  11. Cycling behaviour of sponge-like nanostructured ZnO as thin-film Li-ion battery anodes

    Energy Technology Data Exchange (ETDEWEB)

    Garino, Nadia, E-mail: nadia.garino@iit.it [Center for Space Human Robotics @Polito, Istituto Italiano di Tecnologia, Corso Trento, 21, 10129 Turin (Italy); Lamberti, Andrea; Gazia, Rossana; Chiodoni, Angelica [Center for Space Human Robotics @Polito, Istituto Italiano di Tecnologia, Corso Trento, 21, 10129 Turin (Italy); Gerbaldi, Claudio, E-mail: claudio.gerbaldi@polito.it [Center for Space Human Robotics @Polito, Istituto Italiano di Tecnologia, Corso Trento, 21, 10129 Turin (Italy); GAME Lab, Department of Applied Science and Technology – DISAT, Politecnico di Torino, C.so Duca degli Abruzzi 24, 10129 Turin (Italy)

    2014-12-05

    Highlights: • Zn is thermally oxidized in ambient air to obtain sponge-like ZnO film. • Polycrystalline, transparent, porous thin film is obtained. • Film exhibits stabile specific capacity (∼300 mAh g{sup −1}) after prolonged cycling. • Sponge-like ZnO film shows promising prospects as Li-ion battery anode. - Abstract: Single phase wurtzitic porous ZnO thin films are obtained by a simple two-step method, involving the sputtering deposition of a sponge-like metallic Zn layer, followed by a moderately low temperature treatment for the complete zinc oxidation. Thanks to its 3D nanostructuration, the superimposition of small branches able to grow in length almost isotropically and forming a complex topography, sponge-like ZnO can combine the fast transport properties of one dimensional material and the high surface area usually provided by nanocrystalline electrodes. When galvanostatically tested in lithium cell, after the initial decay, it can provide an almost stable specific capacity higher than 50 μAh cm{sup −2} after prolonged cycling at estimated 0.7 C, with very high Coulombic efficiency.

  12. Cycling behaviour of sponge-like nanostructured ZnO as thin-film Li-ion battery anodes

    International Nuclear Information System (INIS)

    Highlights: • Zn is thermally oxidized in ambient air to obtain sponge-like ZnO film. • Polycrystalline, transparent, porous thin film is obtained. • Film exhibits stabile specific capacity (∼300 mAh g−1) after prolonged cycling. • Sponge-like ZnO film shows promising prospects as Li-ion battery anode. - Abstract: Single phase wurtzitic porous ZnO thin films are obtained by a simple two-step method, involving the sputtering deposition of a sponge-like metallic Zn layer, followed by a moderately low temperature treatment for the complete zinc oxidation. Thanks to its 3D nanostructuration, the superimposition of small branches able to grow in length almost isotropically and forming a complex topography, sponge-like ZnO can combine the fast transport properties of one dimensional material and the high surface area usually provided by nanocrystalline electrodes. When galvanostatically tested in lithium cell, after the initial decay, it can provide an almost stable specific capacity higher than 50 μAh cm−2 after prolonged cycling at estimated 0.7 C, with very high Coulombic efficiency

  13. A flexible freestanding Si/rGO hybrid film anode for stable Li-ion batteries

    Science.gov (United States)

    Zhang, Haoxuan; Jing, Shilong; Hu, Yanjie; Jiang, Hao; Li, Chunzhong

    2016-03-01

    The fabrication of flexible freestanding electrodes with superior electrochemical performance is challenging now in consumer electronics miniaturization. Herein, we demonstrate a simple and scalable synthesis of hollow silicon nanosheets, which then hybridizes with rGO into flexible films by layer-by-layer assembly process. The resulting Si/rGO films, when applied as a free-standing LIBs anode, exhibit a high reversible specific capacity of 904 mAh g-1 at 200 mA g-1 (about 2 times higher than theoretical value of graphite anode), and meanwhile maintain a long cycle life (650 mAh g-1 after 150 cycles). In addition, a flexible full battery has also been assembled based on the flexible film as an anode and the commercial LiCoO2 as a cathode, which impressively delivers a high specific capacity of 700 and 613 mAh g-1 at 50 mA g-1 after 15 cycles in flat and bent state, respectively. Such intriguing electrochemical performances can be mainly attributed to the two-dimensional hollow nanostructure of silicon and their strong synergistic effect with rGO. It is reckoned that our Si/rGO films are a promising anode for advanced flexible LIBs.

  14. Anodic and air oxidation of niobium studied by ion beam analysis with implanted Xe marker

    International Nuclear Information System (INIS)

    Xe marker implantation and backscattering analysis were used to study the growth mechanism of anodic oxides on niobium. In 5 wt% aqueous ammonium citrate solution, analysis of the Xe marker movement demonstrated that the oxide was formed mainly within the existing oxide through the transport of both niobium cations and oxygen anions from each side when the anodic oxidation was carried out with a constant current density of 1.0 mA cm-2 and a limiting oxidation potential from 60 to 100 V. During anodization, the transport numbers of niobium increased with the elevation of potential. The air oxidation behavior of niobium and the profile of Xe ions at the temperature of 200-500 C were also studied. The growth law of niobium oxide was obtained and no movement of the peak position of Xe ions was observed when the temperature was below 350 C. (orig.)

  15. Spark counting technique with an aluminium oxide film

    International Nuclear Information System (INIS)

    Automatic spark counting of etch-pits on a polycarbonate film produced by nuclear fission fragments is now used for neutron monitoring in several countries. A method was developed using an aluminium oxide film instead of a polycarbonate as the neutron detector. Aluminium oxide films were prepared as follows: A cleaned aluminium plate as an anode and a nickel plate as a cathode were immersed in dilute sulfuric acid solution and electric current flowed between the electrodes at 12degC for 10-30 minutes. Electric current density was about 10 mA/cm2. The aluminium plate was then kept in boiling water for 10-30 minutes for sealing. The thickness of the aluminium oxide layer formed was about 1μm. The aluminium plate attached to a plate of suitable fissionable material, such as uranium or thorium, was irradiated with neutrons and set in a usual spark counter for fission track counting. One electrode was the aluminium plate and the other was an aluminized polyester sheet. Sparked pulses were counted with a usual scaler. The advantage of using spark counting with an aluminium oxide film for neutron monitoring is rapid measurement of neutron exposure, since chemical etching which is indispensable for spark counting with a polycarbonate detector film, is not needed. (H.K.)

  16. CNTs tuning and vertical alignment in anodic aluminium oxide membrane

    Institute of Scientific and Technical Information of China (English)

    Maria Sarno; Diana Sannino; Caterina Leone; Paolo Ciambelli

    2012-01-01

    Anodic aluminium oxide (AAOM) membranes were used for template growth of carbon nanotubes (CNT) inside their pores by chemical vapour deposition (CVD) of different hydrocarbons,in the absence of transition metal catalyst.A composite material,containing one nanotube for each channel,having the same length as the membrane thickness and the external diameter close to the diameter of the membrane holes,was obtained.Yield,selectivity,and quality of CNTs in terms of diameter (up to very thin CNT),carbon order,length,arrangement (i.e.number of tubes for each channel),purity,that are critical requisites for several applications were optimized by investigating the effect of changing the hydrocarbon feedstock gas,also in the presence of hydrogen.The samples produced using methane as a feedstock have a well ordered structure.The role of the alumina channels surface during the CNT growth has been investigated and its catalytic activity has been proved for the first time.

  17. Nanoporous Pirani sensor based on anodic aluminum oxide

    Science.gov (United States)

    Jeon, Gwang-Jae; Kim, Woo Young; Shim, Hyun Bin; Lee, Hee Chul

    2016-09-01

    A nanoporous Pirani sensor based on anodic aluminum oxide (AAO) is proposed, and the quantitative relationship between the performance of the sensor and the porosity of the AAO membrane is characterized with a theoretical model. The proposed Pirani sensor is composed of a metallic resistor on a suspended nanoporous membrane, which simultaneously serves as the sensing area and the supporting structure. The AAO membrane has numerous vertically-tufted nanopores, resulting in a lower measurable pressure limit due to both the increased effective sensing area and the decreased effective thermal loss through the supporting structure. Additionally, the suspended AAO membrane structure, with its outer periphery anchored to the substrate, known as a closed-type design, is demonstrated using nanopores of AAO as an etch hole without a bulk micromachining process used on the substrate. In a CMOS-compatible process, a 200 μm × 200 μm nanoporous Pirani sensor with porosity of 25% was capable of measuring the pressure from 0.1 mTorr to 760 Torr. With adjustment of the porosity of the AAO, the measurable range could be extended toward lower pressures of more than one decade compared to a non-porous membrane with an identical footprint.

  18. Anodic oxidation of oxytetracycline: Influence of the experimental conditions on the degradation rate and mechanism

    OpenAIRE

    Annabel Fernandes; Catarina Oliveira; MARIA J PACHECO; Lurdes Ciríaco; Ana Lopes

    2014-01-01

    The anodic oxidation of oxytetracycline was performed with success using as anode a boron-doped diamond electrode. The experiments were conducted in batch mode, using two different electrochemical cells: an up-flow cell, with recirculation, that was used to evaluate the influence of recirculation flow rate; and a stirred cell, used to determine the influence of the applied current density. Besides oxytetracyclin electrodegradation rate and mineralization extent, oxidation by-products were als...

  19. CdS{sub x}Se{sub 1−x} alloyed quantum dots-sensitized solar cells based on different architectures of anodic oxidation TiO{sub 2} film

    Energy Technology Data Exchange (ETDEWEB)

    Li, Zhen; Yu, Libo; Liu, Yingbo; Sun, Shuqing, E-mail: sunshuqing@tju.edu.cn [Tianjin University, Department of Chemistry (China)

    2014-12-15

    Nanostructured TiO{sub 2} translucent films with different architectures including TiO{sub 2} nanotube (NT), TiO{sub 2} nanowire (NW), and TiO{sub 2} nanowire/nanotube (NW/NT) have been produced by second electrochemical oxidization of TiO{sub 2} NT with diameter around 90–110 nm via modulation of applied voltage. These TiO{sub 2} architectures are sensitized with CdS{sub x}Se{sub 1−x} alloyed quantum dots (QDs) in sizes of around 3–5 nm aiming to tune the response of the photoelectrochemical properties in the visible region. One-step hydrothermal method facilitates the deposition of CdS{sub x}Se{sub 1−x} QDs onto TiO{sub 2} films. These CdS{sub x}Se{sub 1−x} QDs exhibit a tunable range of light absorption with changing the feed molar ratio of S:Se in precursor solution, and inject electrons into TiO{sub 2} films upon excitation with visible light, enabling their application as photosensitizers in sensitized solar cells. Power conversion efficiency (PCE) of 2.00, 1.72, and 1.06 % are achieved with CdS{sub x}Se{sub 1−x} (obtained with S:Se = 0:4) alloyed QDs sensitized solar cells based on TiO{sub 2} NW/NT, TiO{sub 2} NW, and TiO{sub 2} NT architectures, respectively. The significant enhancement of power conversion efficiency obtained with the CdS{sub x}Se{sub 1−x}/TiO{sub 2} NW/NT solar cell can be attributed to the extended absorption of light region tuned by CdS{sub x}Se{sub 1−x} alloyed QDs and enlarged deposition of QDs and efficient electrons transport provided by TiO{sub 2} NW/NT architecture.

  20. Intermediate-Temperature Solid-Oxide Fuel Cells with a Gadolinium-Doped Ceria Anodic Functional Layer Deposited via Radio-Frequency Sputtering.

    Science.gov (United States)

    Tanveer, Waqas Hassan; Ji, Sanghoon; Yu, Wonjong; Cho, Gu Young; Lee, Yoon Ho; Cha, Suk Won

    2015-11-01

    We investigated the effects of the insertion of a gadolinium-doped ceria (GDC) anodic functional layer (AFL) on the electrochemical performance of intermediate-temperature solid-oxide fuel cells (SOFCs). Fully stabilized yttria-stabilized zirconia (YSZ) was used as an oxygen-ion-conducting and support material. Nickel-Samaria-doped ceriathin film was used as an anode material, while screen-printed lanthanum strontium magnetite served as a cathode material. In order to enhance the interfacial reaction on the anode side, a GDC-AFL with a thickness of about 140 nm, deposited via radio-frequency sputtering, was inserted into the anode-electrolyte interface. SOFCs with and without a GDC-AFL were electrochemically characterized. In an intermediate temperature range of about 700 - 800 degrees C, the application of the GDC-AFL led to an increase in the peak power density of approximately 16%.

  1. Low temperature solid oxide fuel cells with proton-conducting Y:BaZrO3 electrolyte on porous anodic aluminum oxide substrate

    International Nuclear Information System (INIS)

    This paper presents the architecture of a nano thin-film yttrium-doped barium zirconate (BYZ) solid-oxide fuel cell that uses nanoporous anodic aluminum oxide (AAO) as a supporting and gas-permeable substrate. The anode was fabricated by sputtering 300 nm platinum thin film that partially covered the AAO surface pores, followed by an additional conformal platinum coating to tune the pore size by atomic layer deposition. Two different nano-porous anode structures with a pore size of 10 nm or 50 nm were deposited. Proton-conducting BYZ ceramic electrolyte with increasing thicknesses of 300, 600, and 900 nm was deposited on top of the platinum anode by pulsed laser deposition, followed by a 200 nm layer of porous Pt sputtered on BYZ electrolyte as a cathode. The open circuit voltage (OCV) of the fuel cells was characterized at 250 °C with 1:1 volumetric stoichiometry of a methanol/water vapor mixture as the fuel. The OCVs were 0.17 V with a 900 nm-thick BYZ electrolyte on 50 nm pores and 0.3 V with a 600 nm-thick BYZ electrolyte on 10 nm pores, respectively, but it increased to 0.8 V for a 900 nm-thick BYZ electrolyte on 10 nm pores, indicating that increasing the film thickness and decreasing a surface pore size help to reduce the number of electrolyte pinholes and the gas leakage through the electrolyte. A maximum power density of 5.6 mW/cm2 at 250 °C was obtained from the fuel cell with 900 nm of BYZ electrolyte using methanol vapor as a fuel. - Highlights: • A low temperature ceramic fuel cell on nano-porous substrate was demonstrated. • A thin-film yttrium doped barium zirconate (BYZ) was deposited as an electrolyte. • An open circuit voltage (OCV) was measured to verify the BYZ film quality. • An OCV increased by increasing BYZ film thickness and decreasing pore size of anode. • The current–voltage performance was measured using vaporized methanol fuel at 250 °C

  2. Low temperature solid oxide fuel cells with proton-conducting Y:BaZrO{sub 3} electrolyte on porous anodic aluminum oxide substrate

    Energy Technology Data Exchange (ETDEWEB)

    Ha, Seungbum [School of Mechanical and Aerospace Engineering, Nanyang Technological University, 50 Nanyang Avenue, Singapore 639798 (Singapore); School of Mechanical and Aerospace Engineering, Seoul National University, Daehak-dong, Gwanak-gu, Seoul 151–742 (Korea, Republic of); Su, Pei-Chen [School of Mechanical and Aerospace Engineering, Nanyang Technological University, 50 Nanyang Avenue, Singapore 639798 (Singapore); Ji, Sanghoon [Graduate School of Convergence Science and Technology, Seoul National University, Daehak-dong, Gwanak-gu, Seoul 151–742 (Korea, Republic of); Cha, Suk Won, E-mail: swcha@snu.ac.kr [School of Mechanical and Aerospace Engineering, Seoul National University, Daehak-dong, Gwanak-gu, Seoul 151–742 (Korea, Republic of)

    2013-10-01

    This paper presents the architecture of a nano thin-film yttrium-doped barium zirconate (BYZ) solid-oxide fuel cell that uses nanoporous anodic aluminum oxide (AAO) as a supporting and gas-permeable substrate. The anode was fabricated by sputtering 300 nm platinum thin film that partially covered the AAO surface pores, followed by an additional conformal platinum coating to tune the pore size by atomic layer deposition. Two different nano-porous anode structures with a pore size of 10 nm or 50 nm were deposited. Proton-conducting BYZ ceramic electrolyte with increasing thicknesses of 300, 600, and 900 nm was deposited on top of the platinum anode by pulsed laser deposition, followed by a 200 nm layer of porous Pt sputtered on BYZ electrolyte as a cathode. The open circuit voltage (OCV) of the fuel cells was characterized at 250 °C with 1:1 volumetric stoichiometry of a methanol/water vapor mixture as the fuel. The OCVs were 0.17 V with a 900 nm-thick BYZ electrolyte on 50 nm pores and 0.3 V with a 600 nm-thick BYZ electrolyte on 10 nm pores, respectively, but it increased to 0.8 V for a 900 nm-thick BYZ electrolyte on 10 nm pores, indicating that increasing the film thickness and decreasing a surface pore size help to reduce the number of electrolyte pinholes and the gas leakage through the electrolyte. A maximum power density of 5.6 mW/cm{sup 2} at 250 °C was obtained from the fuel cell with 900 nm of BYZ electrolyte using methanol vapor as a fuel. - Highlights: • A low temperature ceramic fuel cell on nano-porous substrate was demonstrated. • A thin-film yttrium doped barium zirconate (BYZ) was deposited as an electrolyte. • An open circuit voltage (OCV) was measured to verify the BYZ film quality. • An OCV increased by increasing BYZ film thickness and decreasing pore size of anode. • The current–voltage performance was measured using vaporized methanol fuel at 250 °C.

  3. Conversion Reaction-Based Oxide Nanomaterials for Lithium Ion Battery Anodes.

    Science.gov (United States)

    Yu, Seung-Ho; Lee, Soo Hong; Lee, Dong Jun; Sung, Yung-Eun; Hyeon, Taeghwan

    2016-04-01

    Developing high-energy-density electrodes for lithium ion batteries (LIBs) is of primary importance to meet the challenges in electronics and automobile industries in the near future. Conversion reaction-based transition metal oxides are attractive candidates for LIB anodes because of their high theoretical capacities. This review summarizes recent advances on the development of nanostructured transition metal oxides for use in lithium ion battery anodes based on conversion reactions. The oxide materials covered in this review include oxides of iron, manganese, cobalt, copper, nickel, molybdenum, zinc, ruthenium, chromium, and tungsten, and mixed metal oxides. Various kinds of nanostructured materials including nanowires, nanosheets, hollow structures, porous structures, and oxide/carbon nanocomposites are discussed in terms of their LIB anode applications. PMID:26627913

  4. Performance of alternative oxide anodes for the electrochemical oxidation of hydrogen and methane in solid oxide fuel cells

    Energy Technology Data Exchange (ETDEWEB)

    Tu, H.; Apfel, H.; Stimming, U. [Department of Physics E19, Technical University of Munich, James-Franck-Strasse 1, D-85748 Garching (Germany)

    2006-07-15

    The electrode performances of the alternative oxides: La{sub 0.05}Ca{sub 0.95}Cr{sub 0.05}Ti{sub 0.95}O{sub 3-{delta}}-8YSZ and Ce{sub 0.8}TM{sub 0.2}O{sub 2-{delta}}(TM=Mn, Co) for the direct electrochemical oxidation of methane are investigated to assess their potential as anode materials for efficient methane conversion in a SOFC. The electrochemical oxidation of hydrogen was also studied, for comparison. The oxides are characterised electrochemically with impedance spectroscopy in the frequency range from 10 mHz to 1MHz, using a three-electrode geometry. They are compared to a standard Ni/8YSZ anode for the electrochemical oxidation of hydrogen. It is found that La{sub 0.05}Ca{sub 0.95}Cr{sub 0.05}Ti{sub 0.95}O{sub 3-{delta}}-8YSZ demonstrates a poor electrochemical activity in both hydrogen and methane. However, the electrochemical activity of Ce{sub 0.8}Mn{sub 0.2}O{sub 2-{delta}} is promising, but the electronic conductivity needs to be increased, e.g., by adding a conducting oxide, before it can be used as an anode material in a SOFC. (Abstract Copyright [2006], Wiley Periodicals, Inc.)

  5. Effects of Anodic Voltages on Microstructure and Properties of Plasma Electrolytic Oxidation Coatings on Biomedical NiTi Alloy

    Institute of Scientific and Technical Information of China (English)

    Jilin Xu; Fu Liu; Junming Luo; Liancheng Zhao

    2013-01-01

    Plasma electrolytic oxidation (PEO) coatings,formed under various anodic voltages (320-440 V) on biomedical NiTi alloy,are mainly composed of γ-Al2O3 crystal phase.The evolution of discharging sparks during the PEO process under different anodic voltages was observed.The surface and cross-sectional morphologies,composition,bonding strength,wear resistance and corrosion resistance of the coatings were investigated by scanning electron microscopy (SEM),thin-film X-ray diffraction (TF-XRD),energy dispersive X-ray spectrometry (EDS),surface roughness,direct pull-off test,ball-on-disk friction and wear test and potentiodynamic polarization test,respectively.The results showed that the evolution of discharging sparks during the PEO process directly influenced the microstructure of the PEO coatings and further influences the properties.When the anodic voltage increased from 320 V to 400 V,the corrosion resistance and wear resistance of the coatings slowly increased,and all the bonding strength was higher than 60 MPa; further increasing the anodic voltages,especially up to 440 V,although the thickness and γ-Al2O3 crystallinity of the coatings further increased,the microstructure and properties of the coatings were obviously deteriorated.

  6. UV-treated graphene oxide as anode interfacial layers for P3HT : PCBM solar cells

    Science.gov (United States)

    Cheng, Cheng-En; Tsai, Cheng-Wei; Pei, Zingway; Lin, Tsung-Wu; Chang, Chen-Shiung; Shih-Sen Chien, Forest

    2015-06-01

    Solution-processable graphene oxide (GO) ultrathin films were introduced as anode interfacial layers (AILs) for polymer solar cells (PSCs). The photovoltaic performance of PSCs containing thermal- and UV-treated GO was comparable to that of PSCs with conventional poly(3,4-ethyledioxythiphene):poly(styrenesulfonate) AILs. UV treatment induced the surface activation of GO; an increase in the work function of UV-treated GO improved the energy band alignment at the GO/poly(3-hexylthiophene) interface, which accounted for the efficient hole collection and photovoltaic performance of PSCs with treated GO.

  7. Electrochemical Impedance Spectroscopy Illuminating Performance Evolution of Porous Core–Shell Structured Nickel/Nickel Oxide Anode Materials

    International Nuclear Information System (INIS)

    Highlights: • The electrochemical reaction kinetics of the Ni/NiO anode was studied for the first time. • Charge transfer resistance is main contribution to total resistance during discharge process. • The slow growth of the SEI film is responsible for the capacity fading upon cycling. • Some promising strategies to optimize NiO anode performance were summarized. - Abstract: The electrochemical reaction kinetics of the porous core–shell structured Ni/NiO anode for Li ion battery application is systematically investigated by monitoring the electrochemical impedance evolution for the first time. The electrochemical impedance under prescribed condition is measured by using impedance spectroscopy in equilibrium conditions at various depths of discharge (DOD) during charge–discharge cycles. The Nyquist plots of the binder-free porous Ni/NiO electrode are interpreted with a selective equivalent circuit composed of solution resistance, solid electrolyte interphase (SEI) film, charge transfer and solid state diffusion. The impedance analysis shows that the change of charge transfer resistance is the main contribution to the total resistance change during discharge, and the surface configuration of the obtained electrode may experience significant change during the first two cycles. Meanwhile, the increase of internal resistance reduced the utilization efficiency of the active material may be another convincing factor to increase the irreversible capacity. In addition, the impedance evolution of the as-prepared electrode during charge–discharge cycles reveals that the slow growth of the SEI film is responsible for the capacity fading after long term cycling. As a result, several strategies are summarized to optimize the electrochemical performances of transition metal oxide anodes for lithium ion batteries

  8. Influence of silicon on the growth of barrier-type anodic films on titanium

    OpenAIRE

    Tanvir, M. Tauseef; Fushimi, K; Shimizu, K.; Nagata, S; Skeldon, P; Thompson, G.E.; Habazaki, H.

    2007-01-01

    Amorphous anodic titania, stabilised by incorporation of silicon species, is shown to grow to high voltages on sputter-deposited, single-phase Ti–Si alloys during anodizing at a constant current density in ammonium pentaborate electrolyte. The films comprise two main layers, with silicon species confined to the inner layers. An amorphous-to-crystalline transition occurs at 60 V on the Ti–6 at.% Si alloy, while the transition is suppressed to voltages above 140 V on alloys with 12 and 26 at.% ...

  9. Effects of anodic passivation on the constitution, stability and resistance to corrosion of passive film formed on an Fe-24Mn-4Al-5Cr alloy

    International Nuclear Information System (INIS)

    The effects of anodic aging time and potential on the corrosion resistance, stability and constitution of the passive film formed on an Fe-24Mn-4Al-5Cr alloy in 50% HNO3 solution were studied by using combined electrochemical measurements and Auger electron spectroscopic (AES)/X-ray photoelectron spectroscopic (XPS) analysis. In the anodic passive region, prolonged anodic aging time or increased passivating potential can induce better protective and stable properties of the passive film and better resistance to corrosion. With increasing aging time from 15 min to 5 h, the time required for the potential decay from the passive to active state increases from about 300 up to above 12,000 s, and the corrosion resistance in 1 mol l-1 Na2SO4 solution of Fe-24Mn-4Al-5Cr alloy, characterized by polarization curves, is superior to that of Fe-13% Cr-0.1% C stainless steel. AES and XPS analyses of the aging passive film show that these improvements of properties are related to modifications of the passive layer with time. The increase of resistance to corrosion is attributed to Al2O3 and Cr2O3 enrichment and oxides of Fe and Mn depletion in the passive film and a thickening of the effective barrier layer of oxides

  10. Electro-Oxidation of Concentrated Ce(Ⅲ) at Carbon Felt Anode in Nitric Acid Media

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    Electro-oxidation of Ce( Ⅲ) to Ce( Ⅳ ) in parallel plate flow type electrolyzer divided with cation exchange membrane was carried out in nitric acid media at carbon felt anode under galvanostatic conditions. Carbon felt was used as an anode for its high specific surface area and high oxygen evolution overpotential. Pt coated Ti plates were used as cathcurrent efficiency (92%) until about 80% of Ce( Ⅲ) was oxidized. Then, oxygen evolution, accompanied by terminal voltage jump, took place, lowering current efficiency. Ce( Ⅲ ) was oxidized up to 90% with current efficiency of 62%. In this mode, strong carbon felt anode oxidation was observed. The wear out of carbon felt was 46% in six consequent runs (6 h of operation). After each run, carbon felt surface had to be renewed with slightly alkaline solution to remove carbon oxidation products and ensure regular operational conditions. When anode surface was blocked, oxygen evolution took place from the beginning of electrolysis due to higher actual current density. The wear out of carbon felt anode could be minimized by means of oxygen evolution prevention. In the case when electrolysis had been stopped before oxygen evolution started (at Ce( Ⅳ ) conversion of about 80% ), the wear out of anode was less than 2% during 6 consequent runs (4 h of operation).

  11. Effect of Solution Temperature for Al Alloy Anodizing on Cavitation Characteristics

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Seung-Jun [Kunsan National University, Kunsan (Korea, Republic of); Lee, Jung Hyung; Kim, Seong Jong [Mokpo National Maritime University, Haeyangdaehak-ro 91, Mokpo (Korea, Republic of)

    2015-06-15

    The commercialization of aluminum had been delayed than other metals because of its high oxygen affinity. Anodizing is a process in which oxide film is formed on the surface of a valve metal in an electrolyte solution by anodic oxidation reaction. Aluminum has thin oxide film on surface but the oxide film is inhomogeneous having a thickness only in the range of several nanometers. Anodizing process increases the thickness of the oxide film significantly. In this study, porous type oxide film was produced on the surface of aluminum in sulfuric acid as a function of electrolyte temperature, and the optimum condition were determined for anodizing film to exhibit excellent cavitation resistance in seawater environment. The result revealed that the oxide film formed at 10 ℃ represented the highest cavitation resistance, while the oxide film formed at 15 ℃ showed the lowest resistance to cavitation in spite of its high hardness.

  12. Comparison of Anodic Community in Microbial Fuel Cells with Iron Oxide-Reducing Community.

    Science.gov (United States)

    Yokoyama, Hiroshi; Ishida, Mitsuyoshi; Yamashita, Takahiro

    2016-04-28

    The group of Fe(III) oxide-reducing bacteria includes exoelectrogenic bacteria, and they possess similar properties of transferring electrons to extracellular insoluble-electron acceptors. The exoelectrogenic bacteria can use the anode in microbial fuel cells (MFCs) as the terminal electron acceptor in anaerobic acetate oxidation. In the present study, the anodic community was compared with the community using Fe(III) oxide (ferrihydrite) as the electron acceptor coupled with acetate oxidation. To precisely analyze the structures, the community was established by enrichment cultures using the same inoculum used for the MFCs. High-throughput sequencing of the 16S rRNA gene revealed considerable differences between the structure of the anodic communities and that of the Fe(III) oxide-reducing community. Geobacter species were predominantly detected (>46%) in the anodic communities. In contrast, Pseudomonas (70%) and Desulfosporosinus (16%) were predominant in the Fe(III) oxide-reducing community. These results demonstrated that Geobacter species are the most specialized among Fe(III)-reducing bacteria for electron transfer to the anode in MFCs. In addition, the present study indicates the presence of a novel lineage of bacteria in the genus Pseudomonas that highly prefers ferrihydrite as the terminal electron acceptor in acetate oxidation. PMID:26767577

  13. Efficient processing of reaction-sintered silicon carbide by anodically oxidation-assisted polishing

    Science.gov (United States)

    Tu, Qunzhang; Shen, Xinmin; Zhou, Jianzhao; He, Xiaohui; Yamamura, Kazuya

    2015-10-01

    Reaction-sintered silicon carbide (RS-SiC) is a promising optical material for the space telescope systems. Anodically oxidation-assisted polishing is a method to machine RS-SiC. The electrolyte used in this study is a mixture of hydrogen peroxide (H2O2) and hydrochloric acid (HCl), and the oxidation potential has two modes: constant potential and high-frequency-square-wave potential. Oxide morphologies are compared by scanning electron microscope/energy dispersive x-ray spectroscopy and scanning white-light interferometer. The results indicate that anodic oxidation under constant potential can not only obtain a relatively smooth surface but also be propitious to obtain high material removal rate. The oxidation depth in anodic oxidation under constant potential is calculated by comparing surface morphologies before and after hydrofluoric acid etching. The theoretical oxidation rate is 5.3 nm/s based on the linear Deal-Grove model. Polishing of the oxidized RS-SiC is conducted to validate the machinability of the oxide layer. The obtained surface roughness root-mean-square is around 4.5 nm. Thus, anodically oxidation-assisted polishing can be considered as an efficient method, which can fill the performance gap between the rough figuring and fine finishing of RS-SiC. It can improve the machining quality of RS-SiC parts and promote the application of RS-SiC products.

  14. Effects of Oxide Film on the Corrosion Resistance of Titanium Grade 7 in Fluoride-Containing NaCl Brines

    Energy Technology Data Exchange (ETDEWEB)

    Lian, T; Whalen, M T; Wong, L

    2004-11-30

    The effects of oxide film on the corrosion behavior of Titanium Grade 7 (0.12-0.25% Pd) in fluoride-containing NaCl brines have been investigated. With the presence of a 0.6 {micro}m thick oxide layer, the annealed Ti grade 7 exhibited a significant improvement on the anodic polarization behavior. However, the oxide film did not demonstrate sustainable corrosion resistance in fluoride-containing solutions.

  15. Facile synthesis of a mechanically robust and highly porous NiO film with excellent electrocatalytic activity towards methanol oxidation

    Science.gov (United States)

    Wang, Luoyuan; Zhang, Guoge; Liu, Yan; Li, Wenfang; Lu, Wei; Huang, Haitao

    2016-05-01

    Considerable research is being conducted in searching for effective anode catalysts in alkaline direct methanol fuel cells (DMFCs). Although significant progress has been achieved, it is still challenging to prepare non-Pt catalysts with both excellent activity and good durability. Herein, a highly porous NiO film is developed by a facile and fast anodization approach. The anodic NiO film demonstrates a high surface area, large mesopore volume and small crystallite size, leading to facilitated adsorption of reaction species, easy electrolyte penetration and fast reaction kinetics. Furthermore, as anodic NiO is grown in situ on a metallic substrate with strong adhesion strength and good electrical contact, it can be used directly as an anode catalyst for methanol oxidation without the need to add any binder or conducting agent. Such an additive-free approach greatly expedites the catalyst preparation process. The anodic NiO shows lower methanol oxidation potential, higher oxidation current and better catalytic durability than most of the state-of-the-art Ni-based catalysts reported elsewhere. As anodization is a simple, low cost and easily scaled up method, the work described here provides an exciting direction to speed up the practical application of alkaline DMFCs.Considerable research is being conducted in searching for effective anode catalysts in alkaline direct methanol fuel cells (DMFCs). Although significant progress has been achieved, it is still challenging to prepare non-Pt catalysts with both excellent activity and good durability. Herein, a highly porous NiO film is developed by a facile and fast anodization approach. The anodic NiO film demonstrates a high surface area, large mesopore volume and small crystallite size, leading to facilitated adsorption of reaction species, easy electrolyte penetration and fast reaction kinetics. Furthermore, as anodic NiO is grown in situ on a metallic substrate with strong adhesion strength and good electrical contact

  16. Facile synthesis of reduced graphene oxide-porous silicon composite as superior anode material for lithium-ion battery anodes

    Science.gov (United States)

    Jiao, Lian-Sheng; Liu, Jin-Yu; Li, Hong-Yan; Wu, Tong-Shun; Li, Fenghua; Wang, Hao-Yu; Niu, Li

    2016-05-01

    We report a new method for synthesizing reduced graphene oxide (rGO)-porous silicon composite for lithium-ion battery anodes. Rice husks were used as a as a raw material source for the synthesis of porous Si through magnesiothermic reduction process. The as-obtained composite exhibits good rate and cycling performance taking advantage of the porous structure of silicon inheriting from rice husks and the outstanding characteristic of graphene. A considerably high delithiation capacity of 907 mA h g-1 can be retained even at a rate of 16 A g-1. A discharge capacity of 830 mA h g-1 at a current density of 1 A g-1 was delivered after 200 cycles. This may contribute to the further advancement of Si-based composite anode design.

  17. Fabrication and Characterization of Graded Anodes for Anode-Supported Solid Oxide Fuel Cells by Tape Casting and Lamination

    DEFF Research Database (Denmark)

    Beltran-Lopez, J.F.; Laguna-Bercero, M.A.; Gurauskis, Jonas;

    2014-01-01

    Graded anodes for anode-supported solid oxide fuel cells (SOFCs) are fabricated by tape casting and subsequent cold lamination of plates using different compositions. Rheological parameters are adjusted to obtain stable suspensions for tape casting. The conditions for the tape casting...... and homogeneous distribution of nickel, zirconia, and pores. The laminated samples showed a total porosity of 18.7%(in vol%) and a bimodal pore size distribution centered in 20 and 150 nm, and the measured electrical resistivity of this sample was 120±12 μΩ cm. The novelty of the present work is the lamination...... of tapes at room temperature without using plasticizers. This is made by the combination of two different binders with varying Tg (glass transition temperature) which resulted in plastic deformation at room temperature. Those results indicate that the proposed process is a cost-effective method...

  18. Morphology, structural and optical properties of iron oxide thin film photoanodes in photoelectrochemical cell: Effect of electrochemical oxidation

    Science.gov (United States)

    Maabong, Kelebogile; Machatine, Augusto G.; Hu, Yelin; Braun, Artur; Nambala, Fred J.; Diale, Mmantsae

    2016-01-01

    Hematite (α-Fe2O3) is a promising semiconductor as photoanode in solar hydrogen production from photoelectrolysis of water due to its appropriate band gap, low cost and high electrochemical stability in aqueous caustic electrolytes. Operation of such photoanode in a biased photoelectrochemical cell constitutes an anodization with consequent redox reactions at the electrode surface. α-Fe2O3 thin film photoanodes were prepared by simple and inexpensive dip coating method on fluorine doped tin oxide (FTO) glass substrate, annealed in air at 500 °C for 2 h, then electrochemically oxidized (anodized) in 1 M KOH at 500 mV for 1 min in dark and light conditions. Changes in structural properties and morphology of α-Fe2O3 nanoparticles films were investigated by XRD, Raman spectroscopy and a high resolution FE-SEM. The average grain size was observed to increase from ~57 nm for pristine samples to 73 and 77 nm for anodized samples in dark and light respectively. Broadening and red shift in Raman spectra in anodized samples may be attributed to lattice expansion upon oxidation. The UV-visible measurements revealed enhanced absorption in the photoanodes after the treatment. The findings suggest that the anodization of the photoelectrode in a biased cell causes not only changes of the molecular structure at the surface, but also changes in the crystallographic structure which can be detected with x-ray diffractometry.

  19. Semi-transparent ordered TiO2 nanostructures prepared by anodization of titanium thin films deposited onto the FTO substrate

    Science.gov (United States)

    Szkoda, Mariusz; Lisowska-Oleksiak, Anna; Grochowska, Katarzyna; Skowroński, Łukasz; Karczewski, Jakub; Siuzdak, Katarzyna

    2016-09-01

    In a significant amount of cases, the highly ordered TiO2 nanotube arrays grow through anodic oxidation of a titanium metal plate immersed in electrolyte containing fluoride ions. However, for some practical applications, e.g. solar cells or electrochromic windows, the semi-transparent TiO2 formed directly on the transparent, conductive substrate is very much desired. This work shows that high-quality Ti coating could be formed at room temperature using an industrial magnetron sputtering system within 50 min. Under optimized conditions, the anodization process was performed on 2 μm titanium films deposited onto the FTO (fluorine-tin-oxide) support. Depending on the electrolyte type, highly ordered tubular or porous titania layers were obtained. The fabricated samples, after their thermal annealing, were investigated using scanning electron microscopy, Raman spectroscopy and UV-vis spectroscopy in order to investigate their morphology, crystallinity and absorbance ability. The photocurrent response curves indicate that materials are resistant to the photocorrosion process and their activity is strongly connected to optical properties. The most transparent TiO2 films were fabricated when Ti was anodized in water electrolyte, whereas the highest photocurrent densities (12 μA cm-2) were registered for titania received after Ti anodization in ethylene glycol solution. The obtained results are of significant importance in the production of thin, semi-transparent titania nanostructures on a commercial scale.

  20. Tricolor microcavity OLEDs based on P-nc-Si:H films as the complex anodes

    Institute of Scientific and Technical Information of China (English)

    Li Yang; Liu Xingyuan; Wu Chunya; Meng Zhiguo; Wang Yi; Xiong Shaozhen

    2009-01-01

    A P+-nc-Si:H film (boron-doped nc-Si:H thin film) was used as a complex anode of an OLED. As an ideal candidate for the composite anode, the P+-nc-Si:H thin film has a good conductivity with a high work function (~5.7 eV) and outstanding optical properties of high reflectivity, transmission, and a very low absorption. As a result, the combination of the relatively high reflectivity of a P+-nc-Si:H film/ITO complex anode with the very high reflectivity of an Al cathode could form a micro-cavity structure with a certain Q to improve the efficiency of the OLED fabricated on it. An RGB pixel generated by microcavity OLEDs is beneficial for both the reduction of the light loss and the improvement of the color purity and the efficiency. The small molecule Alq would be useful for the emitting light layer (EML) of the MOLED, and the P+-nc-Si film would be used as a complex anode of the MOLED, whose configuration can be constructed as Glass/LTO/P+-nc-Si:H/ITO/MoO3/NPB/Alq/LiF/Al. By adjusting the thickness of the organic layer NPB/Alq, the optical length of the microcavity and the REB colors of the device can be obtained. The peak wavelengths of an OLED are located at 486, 550, and 608 nm, respectively.The CIE coordinates are (0.21,0.45), (0.33,0.63), and (0.54,0.54), and the full widths at half maximum (FWHM)are 35, 32, and 39 nm for red, green, and blue, respectively.

  1. Fluorine-Doped Tin Oxide Nanocrystal/Reduced Graphene Oxide Composites as Lithium Ion Battery Anode Material with High Capacity and Cycling Stability.

    Science.gov (United States)

    Xu, Haiping; Shi, Liyi; Wang, Zhuyi; Liu, Jia; Zhu, Jiefang; Zhao, Yin; Zhang, Meihong; Yuan, Shuai

    2015-12-16

    Tin oxide (SnO2) is a kind of anode material with high theoretical capacity. However, the volume expansion and fast capability fading during cycling have prevented its practical application in lithium ion batteries. Herein, we report that the nanocomposite of fluorine-doped tin oxide (FTO) and reduced graphene oxide (RGO) is an ideal anode material with high capacity, high rate capability, and high stability. The FTO conductive nanocrystals were successfully anchored on RGO nanosheets from an FTO nanocrystals colloid and RGO suspension by hydrothermal treatment. As the anode material, the FTO/RGO composite showed high structural stability during the lithiation and delithiation processes. The conductive FTO nanocrystals favor the formation of stable and thin solid electrolyte interface films. Significantly, the FTO/RGO composite retains a discharge capacity as high as 1439 mAhg(-1) after 200 cycles at a current density of 100 mAg(-1). Moreover, its rate capacity displays 1148 mAhg(-1) at a current density of 1000 mAg(-1).

  2. Studies on electrochromic properties of nickel oxide thin films prepared by spray pyrolysis technique

    Energy Technology Data Exchange (ETDEWEB)

    Kadam, L.D.; Patil, P.S. [Thin film physics laboratory, Department of Physics, Shivaji University, - 416 004 Kolhapur (India)

    2001-11-01

    Electrochromic nickel oxide thin films were prepared by using a simple and inexpensive spray pyrolysis technique (SPT) onto fluorine-doped tin oxide (FTO) coated glass substrates from nickel chloride solution. Transparent NiO-thin films were obtained at a substrate temperature 350C. The films were cubic NiO with preferred orientation in the (111) direction. Infrared spectroscopy results show presence of free hydroxyl ion and water in nickel oxide thin films. The electrochromic properties of the thin films were studied in an aqueous alkaline electrolyte (0.1M KOH) using cyclic voltammetry (CV), chronoamperometry (CA) and spectrophotometry. The films exhibit anodic electrochromism, changing colour from transparent to black. The colouration efficiency at 630nm was calculated to be 37cm{sup 2}/C.

  3. Oxide ultrathin films science and technology

    CERN Document Server

    Pacchioni, Gianfranco

    2012-01-01

    A wealth of information in one accessible book. Written by international experts from multidisciplinary fields, this in-depth exploration of oxide ultrathin films covers all aspects of these systems, starting with preparation and characterization, and going on to geometrical and electronic structure, as well as applications in current and future systems and devices. From the Contents: Synthesis and Preparation of Oxide Ultrathin FilmsCharacterization Tools of Oxide Ultrathin FilmsOrdered Oxide Nanostructures on Metal SurfacesUnusual Properties of Oxides and Other Insulators in the Ultrathin Li

  4. The simulation of the temperature effects on the microhardness of anodic alumina oxide layers

    Directory of Open Access Journals (Sweden)

    M. Gombár

    2014-01-01

    Full Text Available In order to improve the mechanical properties of the layer deposited by anodic oxidation of aluminum on the material EN AW-1050 H24, in the contribution was investigated the microhardness of the deposited layer as a function of the physic-chemical factors affecting in the process of anodic oxidation at the constant anodic current density J = 3 A.dm-2 in electrolyte formed by sulfuric acid and oxalic acid, with the emphasis on the influence of electrolyte temperature in the range – 1,78 °C to 45,78 °C. The model of the studied dependence was compiled based on mathematical and statistical analysis of matrix from experimental obtained data from composite rotation plan of experiment with five independent variable factors (amount of sulfuric acid in the electrolyte, the amount of oxalic acid in the electrolyte, electrolyte, anodizing time and applied voltage.

  5. The electrochemical oxidation of H{sub 2} and CO at patterned Ni anodes of SOFCs

    Energy Technology Data Exchange (ETDEWEB)

    Utz, Annika

    2011-07-01

    In this work, a deeper understanding of the electrochemical oxidation at SOFC anodes was gained by the experimental characterization of patterned Ni anodes in H{sub 2}-H{sub 2}O and CO-CO{sub 2} atmosphere. By high resolution data analysis, the Line Specific Resistance attributed to charge transfer and its dependencies on gas composition, temperature and polarization voltage were identified. Furthermore, the comparison of the performance of patterned and cermet anodes was enabled using a transmission line model. (orig.)

  6. Effect of substrate temperature on electrochromic properties of spray-deposited Ir-oxide thin films

    Science.gov (United States)

    Patil, P. S.; Kawar, R. K.; Sadale, S. B.

    2005-08-01

    Electrochromic iridium oxide thin films were prepared by using a simple and inexpensive spray pyrolysis technique onto fluorine doped tin oxide (FTO)-coated glass substrates, from iridium chloride solution. The substrate temperature was varied between 250 and 400 °C. The as-deposited samples were amorphous. The electrochromic properties of thin films were studied in aqueous electrolyte (0.5N H 2SO 4) using cyclic voltammetry (CV), chronoamperometry (CA) and spectroelectrochemical techniques. The films exhibit anodic electrochromism upon intercalation and deintercalation of H + ions. The colouration efficiency at 630 nm was calculated and found maximum for I 250 sample, owing its hydration.

  7. Growth of anodic films on compound semiconductor electrodes: InP in aqueous (NH sub 4) sub 2 S

    CERN Document Server

    Buckley, D N

    2002-01-01

    Film formation on compound semiconductors under anodic conditions is discussed. The surface properties of InP electrodes were examined following anodization in a (NH sub 4) sub 2 S electrolyte. The observation of a current peak in the cyclic voltammetric curve was attributed to selective etching of the substrate and a film formation process. AFM images of samples anodized in the sulfide solution revealed surface pitting. Thicker films formed at higher potentials exhibited extensive cracking as observed by optical and electron microscopy, and this was explicitly demonstrated to occur ex situ rather than during the electrochemical treatment. The composition of the thick film was identified as In sub 2 S sub 3 by EDX and XPS. The measured film thickness varies linearly with the charge passed, and comparison between experimental thickness measurements and theoretical estimates for the thickness indicate a porosity of over 70 %. Cracking is attributed to shrinkage during drying of the highly porous film and does n...

  8. Biocatalytic anode for glucose oxidation utilizing carbon nanotubes for direct electron transfer with glucose oxidase

    Energy Technology Data Exchange (ETDEWEB)

    Vaze, Abhay; Hussain, Nighat; Tang, Chi [Department of Chemistry, University of Connecticut, Storrs, CT 06269-3060 (United States); Leech, Donal [School of Chemistry, National University of Ireland, Galway (Ireland); Rusling, James [Department of Chemistry, University of Connecticut, Storrs, CT 06269-3060 (United States); Department of Cell Biology, University of Connecticut Health Center, Farmington, CT 06032 (United States); School of Chemistry, National University of Ireland, Galway (Ireland)

    2009-10-15

    Covalently linked layers of glucose oxidase, single-wall carbon nanotubes and poly-L-lysine on pyrolytic graphite resulted in a stable biofuel cell anode featuring direct electron transfer from the enzyme. Catalytic response observed upon addition of glucose was due to electrochemical oxidation of FADH{sub 2} under aerobic conditions. The electrode potential depended on glucose concentration. This system has essential attributes of an anode in a mediator-free biocatalytic fuel cell. (author)

  9. Enhanced in vitro biological activity generated by surface characteristics of anodically oxidized titanium – the contribution of the oxidation effect

    Directory of Open Access Journals (Sweden)

    Wurihan

    2015-05-01

    Full Text Available Anodically oxidized titanium surfaces, prepared by spark discharge, have micro-submicron surface topography and nano-scale surface chemistry, such as hydrophilic functional groups or hydroxyl radicals in parallel. The complexity of the surface characteristics makes it difficult to draw a clear conclusion as to which surface characteristic, of anodically oxidized titanium, is critical in each biological event. This study examined the in vitro biological changes, induced by various surface characteristics of anodically oxidized titanium with, or without, release of hydroxyl radicals onto the surface. Anodically oxidized titanium enhanced the expression of genes associated with differentiating osteoblasts and increased the degree of matrix mineralization by these cells in vitro. The phenotypes of cells on the anodically oxidized titanium were the same with, or without, release of hydroxyl radicals. However, the nanomechanical properties of this in vitro mineralized tissue were significantly enhanced on surfaces, with release of hydroxyl radicals by oxidation effects. In addition, the mineralized tissue, produced in the presence of bone morphogenetic protein-2 on bare titanium, had significantly weaker nanomechanical properties, despite there being higher osteogenic gene expression levels. We show that enhanced osteogenic cell differentiation on modified titanium is not a sufficient indicator of enhanced in vitro mineralization. This is based on the inferior mechanical properties of mineralized tissues, without either being cultured on a titanium surface with release of hydroxyl radicals, or being supplemented with lysyl oxidase family members.

  10. Structural, optical and electrochromic properties of nickel oxide thin films grown from electrodeposited nickel sulphide

    International Nuclear Information System (INIS)

    Nickel oxide thin films were grown onto FTO-coated glass substrates by a two-step process: electrodeposition of nickel sulphide and their thermal oxidation at 425, 475 and 525 deg. C. The influence of thermal oxidation temperature on structural, optical, morphological and electrochromic properties was studied. The structural properties undoubtedly revealed NiO formation. The electrochromic properties were studied by means of cyclic voltammetry. The films exhibited anodic electrochromism, changing from a transparent state to a coloured state at +0.75 V versus SCE, i.e. by simultaneous ion and electron ejection. The transmittance in the coloured and bleached states was recorded to access electrochromic quality of the films. Colouration efficiency and electrochromic reversibility were found to be maximum (21 mC/cm2 and 89%, respectively) for the films oxidized at 425 deg. C. The optical band gap energy of nickel oxide slightly varies with increase in annealing temperature

  11. Structural, optical and electrochromic properties of nickel oxide thin films grown from electrodeposited nickel sulphide

    Energy Technology Data Exchange (ETDEWEB)

    Uplane, M.M.; Mujawar, S.H.; Inamdar, A.I.; Shinde, P.S.; Sonavane, A.C. [Thin Film Materials Laboratory, Department of Physics, Shivaji University, Kolhapur 416004, Maharashtra (India); Patil, P.S. [Thin Film Materials Laboratory, Department of Physics, Shivaji University, Kolhapur 416004, Maharashtra (India)], E-mail: psp_phy@unishivaji.ac.in

    2007-10-15

    Nickel oxide thin films were grown onto FTO-coated glass substrates by a two-step process: electrodeposition of nickel sulphide and their thermal oxidation at 425, 475 and 525 deg. C. The influence of thermal oxidation temperature on structural, optical, morphological and electrochromic properties was studied. The structural properties undoubtedly revealed NiO formation. The electrochromic properties were studied by means of cyclic voltammetry. The films exhibited anodic electrochromism, changing from a transparent state to a coloured state at +0.75 V versus SCE, i.e. by simultaneous ion and electron ejection. The transmittance in the coloured and bleached states was recorded to access electrochromic quality of the films. Colouration efficiency and electrochromic reversibility were found to be maximum (21 mC/cm{sup 2} and 89%, respectively) for the films oxidized at 425 deg. C. The optical band gap energy of nickel oxide slightly varies with increase in annealing temperature.

  12. Structural, optical and electrochromic properties of nickel oxide thin films grown from electrodeposited nickel sulphide

    Science.gov (United States)

    Uplane, M. M.; Mujawar, S. H.; Inamdar, A. I.; Shinde, P. S.; Sonavane, A. C.; Patil, P. S.

    2007-10-01

    Nickel oxide thin films were grown onto FTO-coated glass substrates by a two-step process: electrodeposition of nickel sulphide and their thermal oxidation at 425, 475 and 525 °C. The influence of thermal oxidation temperature on structural, optical, morphological and electrochromic properties was studied. The structural properties undoubtedly revealed NiO formation. The electrochromic properties were studied by means of cyclic voltammetry. The films exhibited anodic electrochromism, changing from a transparent state to a coloured state at +0.75 V versus SCE, i.e. by simultaneous ion and electron ejection. The transmittance in the coloured and bleached states was recorded to access electrochromic quality of the films. Colouration efficiency and electrochromic reversibility were found to be maximum (21 mC/cm 2 and 89%, respectively) for the films oxidized at 425 °C. The optical band gap energy of nickel oxide slightly varies with increase in annealing temperature.

  13. MoOx thin films deposited by magnetron sputtering as an anode for aqueous micro-supercapacitors

    Directory of Open Access Journals (Sweden)

    Can Liu

    2013-11-01

    Full Text Available In order to examine the potential application of non-stoichiometric molybdenum oxide as anode materials for aqueous micro-supercapacitors, conductive MoOx films (2 ≤ x ≤ 2.3 deposited via RF magnetron sputtering at different temperatures were systematically studied for composition, structure and electrochemical properties in an aqueous solution of Li2SO4. The MoOx (x ≈ 2.3 film deposited at 150 °C exhibited a higher areal capacitance (31 mF cm−2 measured at 5 mV s−1, best rate capability and excellent stability at potentials below −0.1 V versus saturated calomel electrode, compared to the films deposited at room temperature and at higher temperatures. These superior properties were attributed to the multi-valence composition and mixed-phase microstructure, i.e., the coexistence of MoO2 nanocrystals and amorphous MoOx (2.3 < x ≤ 3. A mechanism combining Mo(IV oxidation/reduction on the hydrated MoO2 grain surfaces and cation intercalation/extrusion is proposed to illustrate the pseudo-capacitive process.

  14. Improvement of biological properties of titanium by anodic oxidation and ultraviolet irradiation

    Energy Technology Data Exchange (ETDEWEB)

    Li, Baoe [School of Materials Science and Engineering, Hebei University of Technology, Tianjin 300130 (China); Shanghai Institute of Ceramics, Chinese Academy of Sciences, 1295 Dingxi Road, Shanghai 200050 (China); Li, Ying [Stomatological Hospital, Tianjin Medical University, Tianjin 300070 (China); Li, Jun [School of Materials Science and Engineering, Hebei University of Technology, Tianjin 300130 (China); Fu, Xiaolong; Li, Changyi [Stomatological Hospital, Tianjin Medical University, Tianjin 300070 (China); Wang, Hongshui [School of Materials Science and Engineering, Hebei University of Technology, Tianjin 300130 (China); Liu, Shimin [Business School, Tianjin University of Commerce, Tianjin 300134 (China); Guo, Litong [China University of Mining and Technology, Xuzhou 221116 (China); Xin, Shigang [Shanghai Institute of Ceramics, Chinese Academy of Sciences, 1295 Dingxi Road, Shanghai 200050 (China); Liang, Chunyong, E-mail: liangchunyong@126.com [School of Materials Science and Engineering, Hebei University of Technology, Tianjin 300130 (China); Li, Haipeng, E-mail: lhpcx@163.com [School of Materials Science and Engineering, Hebei University of Technology, Tianjin 300130 (China)

    2014-07-01

    Anodic oxidation was applied to produce a homogeneous and uniform array of nanotubes of about 70 nm on the titanium (Ti) surface, and then, the nanotubes were irradiated by ultraviolet. The bioactivity of the Ti surface was evaluated by simulated body fluid soaking test. The biocompatibility was investigated by in vitro cell culture test. The results showed that bone-like apatite was formed on the anodic oxidized and UV irradiated Ti surface, but not on the as-polished Ti surface after immersion in simulated body fluid for two weeks. Cells cultured on the anodic oxidized Ti surface showed enhanced cell adhesion and proliferation, also presented an up-regulated gene expression of osteogenic markers OPG, compared to those cultured on the as-polished Ti surface. After UV irradiation, the cell behaviors were further improved, indicating better biocompatibility of Ti surface. Based on these results, it can be concluded that anodic oxidation improved the biological properties (bioactivity and biocompatibility) of Ti surface, while UV irradiation improved the biocompatibility to a better extent. The improved biological properties were attributed to the nanostructures as well as the enhanced hydrophilicity. Therefore, anodic oxidation combined with UV irradiation can be used to enhance the biological properties of Ti-based implants.

  15. Electro-oxidation of perfluorooctanoic acid by carbon nanotube sponge anode and the mechanism.

    Science.gov (United States)

    Xue, An; Yuan, Zi-Wen; Sun, Yan; Cao, An-Yuan; Zhao, Hua-Zhang

    2015-12-01

    As an emerging persistent organic pollutant (POPs), perfluorooctanoic acid (PFOA) exists widely in natural environment. It is of particular significance to develop efficient techniques to remove low-concentration PFOA from the contaminated waters. In this work, we adopted a new material, carbon nanotube (CNT) sponge, as electrode to enhance electro-oxidation and achieve high removal efficiency of low-concentration (100μgL(-1)) PFOA from water. CNT sponge was pretreated by mixed acids to improve the surface morphology, hydrophilicity and the content of carbonyl groups on the surface. The highest removal efficiencies for low-concentration PFOA electrolyzed by acid-treated CNT sponge anode proved higher than 90%. The electro-oxidation mechanism of PFOA on CNT sponge anode was also discussed. PFOA is adsorbed on the CNT sponge rapidly increasing the concentration of PFOA on anode surface. When the potential on the anode is adjusted to more than 3.5V, the adsorbed PFOA undergoes electrochemically oxidation and hydrolysis to produce shorter-chain perfluorocarboxylic acids with less CF2 unit. The efficient electro-oxidation of PFOA by CNT sponge anode is due to the combined effect of adsorption and electrochemical oxidation. These findings provide an efficient method to remove actual concentration PFOA from water. PMID:26172515

  16. Development and Testing of High Surface Area Iridium Anodes for Molten Oxide Electrolysis

    Science.gov (United States)

    Shchetkovskiy, Anatoliy; McKechnie, Timothy; Sadoway, Donald R.; Paramore, James; Melendez, Orlando; Curreri, Peter A.

    2010-01-01

    Processing of lunar regolith into oxygen for habitat and propulsion is needed to support future space missions. Direct electrochemical reduction of molten regolith is an attractive method of processing, because no additional chemical reagents are needed. The electrochemical processing of molten oxides requires high surface area, inert anodes. Such electrodes need to be structurally robust at elevated temperatures (1400-1600?C), be resistant to thermal shock, have good electrical conductivity, be resistant to attack by molten oxide (silicate), be electrochemically stable and support high current density. Iridium with its high melting point, good oxidation resistance, superior high temperature strength and ductility is the most promising candidate for anodes in high temperature electrochemical processes. Several innovative concepts for manufacturing such anodes by electrodeposition of iridium from molten salt electrolyte (EL-Form? process) were evaluated. Iridium electrodeposition to form of complex shape components and coating was investigated. Iridium coated graphite, porous iridium structure and solid iridium anodes were fabricated. Testing of electroformed iridium anodes shows no visible degradation. The result of development, manufacturing and testing of high surface, inert iridium anodes will be presented.

  17. Lithium insertion in sputtered vanadium oxide film

    DEFF Research Database (Denmark)

    West, K.; Zachau-Christiansen, B.; Skaarup, S.V.;

    1992-01-01

    were oxygen deficient compared to V2O5. Films prepared in pure argon were reduced to V(4) or lower. The vanadium oxide films were tested in solid-state lithium cells. Films sputtered in oxygen showed electrochemical properties similar to crystalline V2O5. The main differences are a decreased capacity...

  18. Electrochemical quartz crystal microbalance study of polyelectrolyte film growth under anodic conditions

    OpenAIRE

    Nilsson, Sara; Björefors, Fredrik; Robinson, Nathaniel D

    2013-01-01

    Coating hard materials such as Pt with soft polymers like poly-l-lysine is a well-established technique for increasing electrode biocompatibility. We have combined quartz crystal microgravimetry with dissipation with electrochemistry (EQCM-D) to study the deposition of PLL onto Pt electrodes under anodic potentials. Our results confirm the change in film growth over time previously reported by others. However, the dissipation data suggest that, after the short initial phase of the process, th...

  19. Microstructural evolution of tungsten oxide thin films

    International Nuclear Information System (INIS)

    Tungsten oxide thin films are of great interest due to their promising applications in various optoelectronic thin film devices. We have investigated the microstructural evolution of tungsten oxide thin films grown by DC magnetron sputtering on silicon substrate. The structural characterization and surface morphology were carried out using X-ray diffraction and Scanning Electron Microscopy (SEM). The as deposited films were amorphous, where as, the films annealed above 400 deg. were crystalline. In order to explain the microstructural changes due to annealing, we have proposed a 'instability wheel' model for the evolution of the microstructure. This model explains the transformation of mater into various geometries within them selves, followed by external perturbation.

  20. Silicon nitride coated silicon thin film on three dimensions current collector for lithium ion battery anode

    Science.gov (United States)

    Wu, Cheng-Yu; Chang, Chun-Chi; Duh, Jenq-Gong

    2016-09-01

    Silicon nitride coated silicon (N-Si) has been synthesized by two-step DC sputtering on Cu Micro-cone arrays (CMAs) at ambient temperature. The electrochemical properties of N-Si anodes with various thickness of nitride layer are investigated. From the potential window of 1.2 V-0.05 V, high rate charge-discharge and long cycle test have been executed to investigate the electrochemical performances of various N-Si coated Si-based lithium ion batteries anode materials. Higher specific capacity can be obtained after 200 cycles. The cycling stability is enhanced via thinner nitride layer coating as silicon nitride films are converted to Li3N with covered Si thin films. These N-Si anodes can be cycled under high rates up to 10 C due to low charge transfer resistance resulted from silicon nitride films. This indicates that the combination of silicon nitride and silicon can effectively endure high current and thus enhance the cycling stability. It is expected that N-Si is a potential candidate for batteries that can work effectively under high power.

  1. Anode Supported Solid Oxide Fuel Cells - Deconvolution of Degradation into Cathode and Anode Contributions

    DEFF Research Database (Denmark)

    Hagen, Anke; Liu, Yi-Lin; Barfod, Rasmus;

    2007-01-01

    of the cathode were strongly dependent on the pO(2); they were significantly smaller when testing in oxygen compared to air. Microstructural analysis of the cathode/electrolyte interface of a not-tested reference cell carried out after removal of the cathode showed sharp craters on the electrolyte surface where...... the LSM particles had been located. After testing in air, these craters flattened out and decreased in size, indicating the decrease of three phase boundary length. In contrast, they remained almost unchanged after testing in oxygen giving an explanation for the observed smaller - mainly anode related...

  2. Influence of anodization parameters on the volume expansion of anodic aluminum oxide formed in mixed solution of phosphoric and oxalic acids

    Science.gov (United States)

    Kao, Tzung-Ta; Chang, Yao-Chung

    2014-01-01

    The growth of anodic alumina oxide was conducted in the mixed solution of phosphoric and oxalic acids. The influence of anodizing voltage, electrolyte temperature, and concentration of phosphoric and oxalic acids on the volume expansion of anodic aluminum oxide has been investigated. Either anodizing parameter is chosen to its full extent of range that allows the anodization process to be conducted without electric breakdown and to explore the highest possible volume expansion factor. The volume expansion factors were found to vary between 1.25 and 1.9 depending on the anodizing parameters. The variation is explained in connection with electric field, ion transport number, temperature effect, concentration, and activity of acids. The formation of anodic porous alumina at anodizing voltage 160 V in 1.1 M phosphoric acid mixed with 0.14 M oxalic acid at 2 °C showed the peak volume expansion factor of 1.9 and the corresponding moderate growth rate of 168 nm/min.

  3. Mechanical and Abrasive Wear Properties of Anodic Oxide Layers Formed on Aluminium

    Institute of Scientific and Technical Information of China (English)

    W.Bensalah; K.Elleuch; M.Feki; M.Wery; H.F.Ayedi

    2009-01-01

    Aluminium oxide coatings were formed on aluminium substrates in oxalic acid-sulphuric acid bath. Abrasion tests of the obtained anodic layers were carried out on a pin-on-disc machine in accordance with the ISO/DP 825 specifications. The Vickers microhardness, D (HV0.2). and the abrasion weight loss, Wa (mg) were measured. Influence of oxalic acid concentration (Cox), bath temperature (T) and anodic current density (J) on D and Wa has been examined, and the sulphuric acid concentration (Caul) was maintained at 160 g.L-1. It was found that high microhardness and abrasive wear resistance of oxide layers were produced under low temperatures and high current densities with the addition of oxalic acid. The morphology and the composition of the anodic oxide layer were examined by scanning electron microscopy (SEM), atomic force microscopy (AFM), optical microscopy and glow-discharge optical emission spectroscopy (GDOES). It was found that the chemistry of the anodizing electrolyte, temperature, and current density are the controlling factors of the mechanical properties of the anodic oxide layer.

  4. Formation of unidirectional nanoporous structures in thickly anodized aluminum oxide layer

    Institute of Scientific and Technical Information of China (English)

    Hyun-Chae NA; Taek-Jin SUNG; Seok-Heon YOON; Seung-Kyoun HYUN; Mok-Soon KIM; Young-Gi LEE; Sang-Hyun SHIN; Seok-Moon CHOI; Sung YI

    2009-01-01

    A series of anodic aluminum oxide(AAO) was grown on the commercially pure 1050 aluminum sheet by controlling electrolyte temperature (2-15 ℃) and anodizing time (0.5-6 h), using a fixed applied current density of 3 A/dm2 in diluted sulfuric acid electrolyte. A crack-free thick AAO with the thickness of 105-120 ìm and containing unidirectional nano sized pores (average pore diameter of 5-7 nm) is successfully achieved in the specimens anodized for 2 h, irrespective of electrolyte temperature. When anodizing time reaches 6 h, very thick AAO with the thickness of 230-284 ìm is grown, and average diameter of unidirectional pores is in the range of 6-24 nm. The higher values in both the AAO thickness and pore diameter are attained for the specimens anodized at higher temperatures of 10-15 ℃. A crack is observed to exist in the AAO after anodizing up to 4 h and more. A higher fraction (more than 9%) of the crack is shown in the specimens anodized at higher temperatures of 10-15 ℃ for 6 h and a considerable amount of giant cracks are contained.

  5. A novel Ni/ceria-based anode for metal-supported solid oxide fuel cells

    Science.gov (United States)

    Rojek-Wöckner, Veronika A.; Opitz, Alexander K.; Brandner, Marco; Mathé, Jörg; Bram, Martin

    2016-10-01

    For optimization of ageing behavior, electrochemical performance, and sulfur tolerance of metal-supported solid oxide fuel cells a new anode concept is introduced, which is based on a Ni/GDC cermet replacing the established Ni/YSZ anodes. In the present work optimized processing parameters compatible with MSC substrates are specified by doing sintering studies on pressed bulk specimen and on real porous anode structures. The electrochemical performance of the Ni/GDC anodes was characterized by means of symmetrical electrolyte supported model-type cells. In this study, three main objectives are pursued. Firstly, the effective technical realization of the Ni/GDC concept is demonstrated. Secondly, the electrochemical behavior of Ni/GDC porous anodes is characterized by impedance spectroscopy and compared with the current standard Ni/YSZ anode. Further, a qualitative comparison of the sulfur poisoning behavior of both anode types is presented. Thirdly, preliminary results of a successful implementation of the Ni/GDC cermet into a metal-supported single cell are presented.

  6. Conductivity and thermoelectric properties of nanostructure tin oxide thin films

    Directory of Open Access Journals (Sweden)

    M.A. Batal

    2014-04-01

    Full Text Available Tin oxide thin films doped with iron or copper were deposited on glass and porous alumina substrates, using the co-deposition dip coating sol–gel technique. Alumina substrate was prepared by the anodizing technique. Samples were sintered for 2 h at temperature 600 °C. The XRD spectrum of deposited samples shows a polycrystalline structure with a clear characteristic peak of SnO2 cassiterite phase. From (I–V characteristics measured at different temperatures for samples prepared on glass substrates, the density of states at the Fermi level was calculated. Thermoelectric effect was measured with a change of temperature for prepared samples under low pressure 1 mbar. Seebeck coefficient, the carrier concentration, the charge carrier mobility and the figure merit were determined for prepared samples under low pressure 1 mbar. Seebeck coefficient was improved when films were deposited on porous Alumina substrates.

  7. The iron and cerium oxide influence on the electric conductivity and the corrosion resistance of anodized aluminium; A influencia do ferro e do oxido de cerio sobre a condutividade eletrica e a resistencia a corrosao do aluminio anodizado

    Energy Technology Data Exchange (ETDEWEB)

    Souza, Kellie Provazi de

    2006-07-01

    The influence of different treatments on the aluminum system covered with aluminum oxide is investigated. The aluminum anodization in sulphuric media and in mixed sulphuric and phosphoric media was used to alter the corrosion resistance, thickness, coverage degree and microhardness of the anodic oxide. Iron electrodeposition inside the anodic oxide was used to change its electric conductivity and corrosion resistance. Direct and pulsed current were used for iron electrodeposition and the Fe(SO{sub 4}){sub 2}(NH{sub 4}){sub 2}.6H{sub 2}O electrolyte composition was changed with the addition of boric and ascorbic acids. To the sealing treatment the CeCl{sub 3} composition was varied. The energy dispersive x-ray (EDS), the x-ray fluorescence spectroscopy (FRX) and the morphologic analysis by scanning electronic microscopy (SEM) allowed to verify that, the pulsed current increase the iron content inside the anodic layer and that the use of the additives inhibits the iron oxidation. The chronopotentiometric curves obtained during iron electrodeposition indicated that the boric and ascorbic acids mixture increased the electrodeposition process efficiency. The electrochemical impedance spectroscopy (EIE), the Vickers (Hv) microhardness measurements and morphologic analysis evidenced that the sealing treatment improves the corrosion resistance of the anodic film modified with iron. The electrical impedance (EI) technique allowed to prove the electric conductivity increase of the anodized aluminum with iron electrodeposited even after the cerium low concentration treatment. Iron nanowires were prepared by using the anodic oxide pores as template. (author)

  8. Changes in the morphology of porous anodic films formed on aluminium in natural and artificial ageing

    Directory of Open Access Journals (Sweden)

    López, V.

    2003-12-01

    Full Text Available Transmission electron microscopy and electrochemical impedance spectroscopy are used to demonstrate that the water retained in porous anodic aluminium oxide films is the main reason for their reactivity under electron beam irradiation in the TEM, accelerated ageing in an oven at 100 °C, or natural ageing over months and years in an outdoor atmosphere. Though the kinetics in each medium is highly different, there is a clear similarity between the structural and physical-chemical transformations that take place. Unsealed layers, practically free of water, hardly change their structure under the effect of electron beams and show the same impedance plots after hours at 100 °C or after years at environmental temperature in dry atmospheres.

    La microscopía electrónica de transmisión, por una parte, y la espectroscopia de impedancia electroquímica, por otra, demuestran que el agua retenida en las películas anódicas porosas de óxido de aluminio es la principal responsable de su reactividad bajo la irradiación del haz de electrones en el MET, en el envejecimiento acelerado en la estufa a 100 ºC o en el envejecimiento natural de meses y años en la atmósfera a temperatura ambiente. Aunque, de cinéticas muy diferentes, existe una indudable semejanza entre las transformaciones estructurales y físico-químicas que tienen lugar en los tres medios. Las capas sin sellar, prácticamente exentas de agua, apenas cambian su estructura por efecto del haz de electrones y muestran los mismos diagramas de impedancia después de horas a 100 ºC o de años a temperatura ambiente en atmósferas secas.

  9. Building one-dimensional oxide nanostructure arrays on conductive metal substrates for lithium-ion battery anodes.

    Science.gov (United States)

    Jiang, Jian; Li, Yuanyuan; Liu, Jinping; Huang, Xintang

    2011-01-01

    Lithium ion battery (LIB) is potentially one of the most attractive energy storage devices. To meet the demands of future high-power and high-energy density requirements in both thin-film microbatteries and conventional batteries, it is challenging to explore novel nanostructured anode materials instead of conventional graphite. Compared to traditional electrodes based on nanostructure powder paste, directly grown ordered nanostructure array electrodes not only simplify the electrode processing, but also offer remarkable advantages such as fast electron transport/collection and ion diffusion, sufficient electrochemical reaction of individual nanostructures, enhanced material-electrolyte contact area and facile accommodation of the strains caused by lithium intercalation and de-intercalation. This article provides a brief overview of the present status in the area of LIB anodes based on one-dimensional nanostructure arrays growing directly on conductive inert metal substrates, with particular attention to metal oxides synthesized by an anodized alumina membrane (AAM)-free solution-based or hydrothermal methods. Both the scientific developments and the techniques and challenges are critically analyzed.

  10. Performance evaluation of a liquid tin anode solid oxide fuel cell operating under hydrogen, argon and coal

    Science.gov (United States)

    Khurana, Sanchit; LaBarbera, Mark; Fedkin, Mark V.; Lvov, Serguei N.; Abernathy, Harry; Gerdes, Kirk

    2015-01-01

    A liquid tin anode solid oxide fuel cell is constructed and investigated under different operating conditions. Electrochemical Impedance Spectroscopy (EIS) is used to reflect the effect of fuel feed as the EIS spectra changes significantly on switching the fuel from argon to hydrogen. A cathode symmetric cell is used to separate the impedance from the two electrodes, and the results indicate that a major contribution to the charge-transfer and mass-transfer impedance arises from the anode. The OCP of 0.841 V for the cell operating under argon as a metal-air battery indicates the formation of a SnO2 layer at the electrolyte/anode interface. The increase in the OCP to 1.1 V for the hydrogen fueled cell shows that H2 reduces the SnO2 film effectively. The effective diffusion coefficients are calculated using the Warburg element in the equivalent circuit model for the experimental EIS data, and the values of 1.9 10-3 cm2 s-1 at 700 °C, 2.3 10-3 cm2 s-1 at 800 °C and 3.5 10-3 cm2 s-1 at 900 °C indicate the system was influenced by diffusion of hydrogen in the system. Further, the performance degradation over time is attributed to the irreversible conversion of Sn to SnO2 resulting from galvanic polarization.

  11. Studies on anodic oxide coating with low absorptance and high emittance on aluminum alloy 2024

    Energy Technology Data Exchange (ETDEWEB)

    Siva Kumar, C. [Department of Post-graduate studies in Chemistry, Central College, Bangalore (India); Sharma, A.K. [Thermal Process Section, ISRO Satellite Centre, Vimanapura Post, Bangalore (India); Mahendra, K.N.; Mayanna, S.M. [Department of Post-graduate studies in Chemistry, Central College, Bangalore (India)

    2000-01-01

    Anodization of AA 2024 in sulfuric acid bath containing glycerol, lactic acid and ammonium metavenadate has been studied to develop white anodic oxide coating. Investigation on the influence of various operating parameters - coating thickness, current density and ammonium metavenadate concentration on the optical properties was carried out to optimize the process. Infrared, atomic absorption spectroscopic techniques and scanning electron micrograph were used to characterize the coating. The obtained oxide coating provides a ratio of solar absorptance ({alpha}) to infrared emittance ({epsilon}), as low as 0.2. The optical properties and hardness values measured under optimum experimental conditions support its use as a thermal control coating.

  12. Route of electrochemical oxidation of the antibiotic sulfamethoxazole on a mixed oxide anode.

    Science.gov (United States)

    Hussain, Sajjad; Gul, Saima; Steter, Juliana R; Miwa, Douglas W; Motheo, Artur J

    2015-10-01

    The appearance of pharmaceutical compounds and their bioactive transformation products in aquatic environments is becoming an issue of increasing concern. In this study, the electrochemical oxidation of the widely used antibiotic sulfamethoxazole (SMX) was investigated using a commercial mixed oxide anode (Ti/Ru0.3Ti0.7O2) and a single compartment filter press-type flow reactor. The kinetics of SMX degradation was determined as a function of electrolyte composition, applied current density, and initial pH. Almost complete (98 %) degradation of SMX could be achieved within 30 min of electrolysis in 0.1 mol L(-1) NaCl solution at pH 3 with applied current densities ≥20 mA cm(-2). Nine major intermediates of the reaction were identified by LC-ESI-Q-TOF-MS (e.g., C6H9NO2S (m/z = 179), C6H4NOCl (m/z = 141), and C6H6O2 (m/z = 110)). The degradation followed various routes involving cleavage of the oxazole and benzene rings by hydroxyl and/or chlorine radicals, processes that could occur before or after rupture of the N-S bond, followed by oxidation of the remaining moieties. Analysis of the total organic carbon content revealed that the antibiotic was partially mineralized under the conditions employed and some inorganic ions, including NO3 (-) and SO4 (2-), could be identified. The results presented herein demonstrate the efficacy of the electrochemical process using a Ti/Ru0.3Ti0.7O2 anode for the remediation of wastewater containing the antibiotic SMX. PMID:26002364

  13. Novel Combination of Efficient Perovskite Solar Cells with Low Temperature Processed Compact TiO2 Layer via Anodic Oxidation.

    Science.gov (United States)

    Du, Yangyang; Cai, Hongkun; Wen, Hongbin; Wu, Yuxiang; Huang, Like; Ni, Jian; Li, Juan; Zhang, Jianjun

    2016-05-25

    In this work, a facile and low temperature processed anodic oxidation approach is proposed for fabricating compact and homogeneous titanium dioxide film (AO-TiO2). In order to realize morphology and thickness control of AO-TiO2, the theory concerning anodic oxidation (AO) is unveiled and the influence of relevant parameters during the process of AO such as electrolyte ingredient and oxidation voltage on AO-TiO2 formation is observed as well. Meanwhile, we demonstrate that the planar perovskite solar cells (p-PSCs) fabricated in ambient air and utilizing optimized AO-TiO2 as electron transport layer (ETL) can deliver repeatable power conversion efficiency (PCE) over 13%, which possess superior open-circuit voltage (Voc) and higher fill factor (FF) compared to its counterpart utilizing conventional high temperature processed compact TiO2 (c-TiO2) as ETL. Through a further comparative study, it is indicated that the improvement of device performance should be attributed to more effective electron collection from perovskite layer to AO-TiO2 and the decrease of device series resistance. Furthermore, hysteresis effect about current density-voltage (J-V) curves in TiO2-based p-PSCs is also unveiled. PMID:27150310

  14. Durability Prediction of Solid Oxide Fuel Cell Anode Material under Thermo-Mechanical and Fuel Gas Contaminants Effects

    Energy Technology Data Exchange (ETDEWEB)

    Iqbal, Gulfam; Guo, Hua; Kang , Bruce S.; Marina, Olga A.

    2011-01-10

    Solid Oxide Fuel Cells (SOFCs) operate under harsh environments, which cause deterioration of anode material properties and service life. In addition to electrochemical performance, structural integrity of the SOFC anode is essential for successful long-term operation. The SOFC anode is subjected to stresses at high temperature, thermal/redox cycles, and fuel gas contaminants effects during long-term operation. These mechanisms can alter the anode microstructure and affect its electrochemical and structural properties. In this research, anode material degradation mechanisms are briefly reviewed and an anode material durability model is developed and implemented in finite element analysis. The model takes into account thermo-mechanical and fuel gas contaminants degradation mechanisms for prediction of long-term structural integrity of the SOFC anode. The proposed model is validated experimentally using a NexTech ProbostatTM SOFC button cell test apparatus integrated with a Sagnac optical setup for simultaneously measuring electrochemical performance and in-situ anode surface deformation.

  15. Electrochemical combustion of indigo at ternary oxide coated titanium anodes

    Directory of Open Access Journals (Sweden)

    María I. León

    2014-12-01

    Full Text Available The film of iridium and tin dioxides doped with antimony (IrO2-SnO2–Sb2O5 deposited on a Ti substrate (mesh obtained by Pechini method was used for the formation of ·OH radicals by water discharge. Detection of ·OH radicals was followed by the use of the N,N-dimethyl-p-nitrosoaniline (RNO as a spin trap. The electrode surface morphology and composition was characterized by SEM-EDS. The ternary oxide coating was used for the electrochemical combustion of indigo textile dye as a model organic compound in chloride medium. Bulk electrolyses were then carried out at different volumetric flow rates under galvanostatic conditions using a filter-press flow cell. The galvanostatic tests using RNO confirmed that Ti/IrO2-SnO2-Sb2O5 favor the hydroxyl radical formation at current densities between 5 and 7 mA cm-2, while at current density of 10 mA cm-2 the oxygen evolution reaction occurs. The indigo was totally decolorized and mineralized via reactive oxygen species, such as (·OH, H2O2, O3 and active chlorine formed in-situ at the Ti/IrO2-SnO2-Sb2O5 surface at volumetric flow rates between 0.1-0.4 L min-1 and at fixed current density of 7 mA cm-2. The mineralization of indigo carried out at 0.2 L min-1 achieved values of 100 %, with current efficiencies of 80 % and energy consumption of 1.78 KWh m-3.

  16. Liquid crystal alignment in nanoporous anodic aluminum oxide layer for LCD panel applications.

    Science.gov (United States)

    Hong, Chitsung; Tang, Tsung-Ta; Hung, Chi-Yu; Pan, Ru-Pin; Fang, Weileun

    2010-07-16

    This paper reports the implementation and integration of a self-assembled nanoporous anodic aluminum oxide (np-AAO) film and liquid crystal (LC) on an ITO-glass substrate for liquid crystal display (LCD) panel applications. An np-AAO layer with a nanopore array acts as the vertical alignment layer to easily and uniformly align the LC molecules. Moreover, the np-AAO nanoalignment layer provides outstanding material properties, such as being inorganic with good transmittance, and colorless on ITO-glass substrates. In this application, an LCD panel, with the LC on the np-AAO nanoalignment layer, is successfully implemented on an ITO-glass substrate, and its performance is demonstrated. The measurements show that the LCD panel, consisting of an ITO-glass substrate and an np-AAO layer, has a transmittance of 60-80%. In addition, the LCD panel switches from a black state to a bright state at 3 V(rms), with a response time of 62.5 ms. In summary, this paper demonstrates the alignment of LC on an np-AAO layer for LCD applications.

  17. Electrically conducting polymer nanostructures confined in anodized aluminum oxide templates (AAO

    Directory of Open Access Journals (Sweden)

    I. Blaszczyk-Lezak

    2016-03-01

    Full Text Available Intrinsically or extrinsically conducting polymers are considered good candidates for replacement of metals in specific applications. In order to further expand their applications, it seems necessary to examine the influence of confinement effects on the electric properties of nanostructured conducting polymers in comparison to the bulk. The present study reports a novel way to fabricate and characterize high quality and controllable one-dimensional (1D polymer nanostructures with promising electrical properties, with the aid of two examples polyaniline (PANI and poly(vinylidene fluoride with multiwall carbon nanotubes (PVDF-MWCNT as representative of intrinsically and extrinsically conducting polymers, respectively. In this work, porous anodic aluminum oxide (AAO templates have been used both as a nanoreactor to synthesize 1D PANI nanostructures by polymerization of the ANI monomer and as a nanomold to prepare 1D PVDFMWCNT nanorods by melt infiltration of the precursor PVDF-MWCNT film. The obtained polymer nanostructures were morphologically and chemically characterized by SEM and Confocal Raman Spectroscopy, respectively, and the electrical properties determined by Broadband Dielectric Spectroscopy (BDS in a non-destructive way. SEM study allowed to establish the final nanostructure of PANI and PVDF-MWCNT and confirmed, in both cases, the well-aligned and uniform rodlike polymer nanostructures. Confocal Raman Microscopy has been performed to study the formation of the conducting emeraldine salt of PANI through all the length of AAO nanocavities. Finally, the electrical conductivity of both types of polymer nanostructures was easily evaluated by means of Dielectric Spectroscopy.

  18. Preparation of thin hexagonal highly-ordered anodic aluminum oxide (AAO) template onto silicon substrate and growth ZnO nanorod arrays by electrodeposition

    Science.gov (United States)

    Chahrour, Khaled M.; Ahmed, Naser M.; Hashim, M. R.; Elfadill, Nezar G.; Qaeed, M. A.; Bououdina, M.

    2014-12-01

    In this study, anodic aluminum oxide (AAO) templates of Aluminum thin films onto Ti-coated silicon substrates were prepared for growth of nanostructure materials. Hexagonally highly ordered thin AAO templates were fabricated under controllable conditions by using a two-step anodization. The obtained thin AAO templates were approximately 70 nm in pore diameter and 250 nm in length with 110 nm interpore distances within an area of 3 cm2. The difference between first and second anodization was investigated in details by in situ monitoring of current-time curve. A bottom barrier layer of the AAO templates was removed during dropping the voltage in the last period of the anodization process followed by a wet etching using phosphoric acid (5 wt%) for several minutes at ambient temperature. As an application, Zn nanorod arrays embedded in anodic alumina (AAO) template were fabricated by electrodeposition. Oxygen was used to oxidize the electrodeposited Zn nanorods in the AAO template at 700 °C. The morphology, structure and photoluminescence properties of ZnO/AAO assembly were analyzed using Field-emission scanning electron microscope (FESEM), Energy dispersive X-ray spectroscopy (EDX), Atomic force microscope (AFM), X-ray diffraction (XRD) and photoluminescence (PL).

  19. Synthesis, Characterization, and Optimization of Novel Solid Oxide Fuel Cell Anodes

    Science.gov (United States)

    Miller, Elizabeth C.

    This dissertation presents research on the development of novel materials and fabrication procedures for solid oxide fuel cell (SOFC) anodes. The work discussed here is divided into three main categories: all-oxide anodes, catalyst exsolution oxide anodes, and Ni-infiltrated anodes. The all-oxide and catalyst exsolution anodes presented here are further classi?ed as Ni-free anodes operating at the standard 700-800°C SOFC temperature while the Ni-infiltrated anodes operate at intermediate temperatures (≤650°C). Compared with the current state-of-the-art Ni-based cermets, all-oxide, Ni-free SOFC anodes offer fewer coking issues in carbon-containing fuels, reduced degradation due to fuel contaminants, and improved stability during redox cycling. However, electrochemical performance has proven inferior to Ni-based anodes. The perovskite oxide Fe-substituted strontium titanate (STF) has shown potential as an anode material both as a single phase electrode and when combined with Gd-doped ceria (GDC) in a composite electrode. In this work, STF is synthesized using a modified Pechini processes with the aim of reducing STF particle size and increasing the electrochemically active area in the anode. The Pechini method produced particles ? 750 nm in diameter, which is signi°Cantly smaller than the typically micron-sized solid state reaction powder. In the first iteration of anode fabrication with the Pechini powder, issues with over-sintering of the small STF particles limited gas di?usion in the anode. However, after modifying the anode firing temperature, the Pechini cells produced power density comparable to solid state reaction based cells from previous work by Cho et al. Catalyst exsolution anodes, in which metal cations exsolve out of the lattice under reducing conditions and form nanoparticles on the oxide surface, are another Ni-free option for standard operating temperature SOFCs. Little information is known about the onset of nanoparticle formation, which

  20. Application of infiltrated LSCM-GDC oxide anode in direct carbon/coal fuel cells.

    Science.gov (United States)

    Yue, Xiangling; Arenillas, Ana; Irvine, John T S

    2016-08-15

    Hybrid direct carbon/coal fuel cells (HDCFCs) utilise an anode based upon a molten carbonate salt with an oxide conducting solid electrolyte for direct carbon/coal conversion. They can be fuelled by a wide range of carbon sources, and offer higher potential chemical to electrical energy conversion efficiency and have the potential to decrease CO2 emissions compared to coal-fired power plants. In this study, the application of (La, Sr)(Cr, Mn)O3 (LSCM) and (Gd, Ce)O2 (GDC) oxide anodes was explored in a HDCFC system running with two different carbon fuels, an organic xerogel and a raw bituminous coal. The electrochemical performance of the HDCFC based on a 1-2 mm thick 8 mol% yttria stabilised zirconia (YSZ) electrolyte and the GDC-LSCM anode fabricated by wet impregnation procedures was characterized and discussed. The infiltrated oxide anode showed a significantly higher performance than the conventional Ni-YSZ anode, without suffering from impurity formation under HDCFC operation conditions. Total polarisation resistance (Rp) reached 0.8-0.9 Ω cm(2) from DCFC with an oxide anode on xerogel and bituminous coal at 750 °C, with open circuit voltage (OCV) values in the range 1.1-1.2 V on both carbon forms. These indicated the potential application of LSCM-GDC oxide anode in HDCFCs. The chemical compatibility of LSCM/GDC with carbon/carbonate investigation revealed the emergence of an A2BO4 type oxide in place of an ABO3 perovskite structure in the LSCM in a reducing environment, due to Li attack as a result of intimate contact between the LSCM and Li2CO3, with GDC being stable under identical conditions. Such reaction between LSCM and Li2CO3 was not observed on a LSCM-YSZ pellet treated with Li-K carbonate in 5% H2/Ar at 700 °C, nor on a GDC-LSCM anode after HDCFC operation. The HDCFC durability tests of GDC-LSCM oxide on a xerogel and on raw bituminous coal were performed under potentiostatic operation at 0.7 V at 750 °C. The degradation mechanisms were

  1. Oxidation of phenol and chlorophenols on platinized titanium anodes in an acidic medium

    Science.gov (United States)

    Mokbel, Saleh Mohammed; Kolosov, E. N.; Mikhalenko, I. I.

    2016-06-01

    A comparative study of oxidation of phenol, 3-chlorophenol, 4-chlorophenol, and 2,4-dichlorophenol on Pt/Ti and Ce,Pt/Ti electrocatalysts is performed via cyclic voltammetry. It is shown that the surface morphology and roughness of the anode do not change after modification with cerium. The formal kinetic orders of electrooxidation of all compounds are found to be less than one. It is shown that the β temperature coefficients of the rate of oxidation of chlorophenols grow by 10 to 50% when the Ce,Pt/Ti anode is used at a substrate concentration of 1 mM. A tenfold increase in concentration reduces the effect of cerium additive, except for 3-chlorophenol: the latter exhibits a 250% increase in the β value, compared to the Pt/Ti anode.

  2. Influence of Anodic Conditions on Self-ordered Growth of Highly Aligned Titanium Oxide Nanopores

    Directory of Open Access Journals (Sweden)

    Hernández-Vélez M

    2007-01-01

    Full Text Available AbstractSelf-aligned nanoporous TiO2templates synthesized via dc current electrochemical anodization have been carefully analyzed. The influence of environmental temperature during the anodization, ranging from 2 °C to ambient, on the structure and morphology of the nanoporous oxide formation has been investigated, as well as that of the HF electrolyte chemical composition, its concentration and their mixtures with other acids employed for the anodization. Arrays of self-assembled titania nanopores with inner pores diameter ranging between 50 and 100 nm, wall thickness around 20–60 nm and 300 nm in length, are grown in amorphous phase, vertical to the Ti substrate, parallel aligned to each other and uniformly disordering distributed over all the sample surface. Additional remarks about the photoluminiscence properties of the titania nanoporous templates and the magnetic behavior of the Ni filled nanoporous semiconductor Ti oxide template are also included.

  3. A Review of RedOx Cycling of Solid Oxide Fuel Cells Anode

    Directory of Open Access Journals (Sweden)

    Jan Van herle

    2012-08-01

    Full Text Available Solid oxide fuel cells are able to convert fuels, including hydrocarbons, to electricity with an unbeatable efficiency even for small systems. One of the main limitations for long-term utilization is the reduction-oxidation cycling (RedOx cycles of the nickel-based anodes. This paper will review the effects and parameters influencing RedOx cycles of the Ni-ceramic anode. Second, solutions for RedOx instability are reviewed in the patent and open scientific literature. The solutions are described from the point of view of the system, stack design, cell design, new materials and microstructure optimization. Finally, a brief synthesis on RedOx cycling of Ni-based anode supports for standard and optimized microstructures is depicted.

  4. Anode properties of silicon-rich amorphous silicon suboxide films in all-solid-state lithium batteries

    Science.gov (United States)

    Miyazaki, Reona; Ohta, Narumi; Ohnishi, Tsuyoshi; Takada, Kazunori

    2016-10-01

    This paper reports the effects of introducing oxygen into amorphous silicon films on their anode properties in all-solid-state lithium batteries. Although poor cycling performance is a critical issue in silicon anodes, it has been effectively improved by introducing even a small amount of oxygen, that is, even in Si-rich amorphous silicon suboxide (a-SiOx) films. Because of the small amount of oxygen in the films, high cycling performance has been achieved without lowering the capacity and power density: an a-Si film delivers discharge capacity of 2500 mAh g-1 under high discharge current density of 10 mA cm-2 (35 C). These results demonstrate that a-SiOx is a promising candidate for high-capacity anode materials in solid-state batteries.

  5. Sn–Al core–shell nanocomposite as thin film anode for lithium-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Wei, Lin; Zhang, Kai; Tao, Zhanliang, E-mail: taozhl@nankai.edu.cn; Chen, Jun

    2015-09-25

    Highlights: • Sn (core)–Al (shell) nanocomposite thin film is prepared by magnetron sputtering method. • The effect of Al on the structure and electrochemical performance has been investigated. • Improved electrochemical performance is obtained. - Abstract: In this paper, we report on the preparation of Sn (core)–Al (shell) nanocomposite thin films by co-sputtering Sn target and Al target, and their application as anode of lithium-ion batteries. Instrumental analyses of X-ray diffraction, energy dispersive X-ray analysis, scanning electron microscopy, and transmission electron microscope have been used to characterize the structure and morphology. The results reveal that the thin film is composed of core–shell structure with Sn nanoparticle core and Al amorphous shell. Furthermore, measurements of charge–discharge, cyclic voltammetry and electrochemical impedance spectroscopy have been employed to characterize the electrochemical performance of Sn–Al film. The Sn–Al thin film with 18 wt% Al delivers high capacities of 822, 460 and 313 mA h g{sup −1} in the second 2nd, 60th and 200th cycles, respectively. Meanwhile, a discharge capacity of 420 mA h g{sup −1} is obtained at 3000 mA g{sup −1}. The excellent electrochemistry performance is owing to the core–shell structure in which Al shell can alleviate the expansion of volume of Sn particles and restrain the aggregation of Sn particles. The results indicate that Sn–Al thin film is a promising anode for lithium-ion batteries.

  6. Electrochemical Impedance Modeling of a Solid Oxide Fuel Cell Anode

    DEFF Research Database (Denmark)

    Mohammadi, R.; Søgaard, Martin; Ramos, Tania;

    2014-01-01

    A simulation package for the impedance response of SOFC anodes is presented here. The model couples the gas transport in gas channels and within a porous electrode with the electrochemical kinetics. The gas phase mass transport is modeled using mass conservation equations. A transmission line model...... (TLM), which is suitably modified to account for the electrode microstructural details, is used for modeling the impedance arising from the electrochemical reactions. In order to solve the system of nonlinear equations, an in-house code based on the finite difference method was developed. Some...

  7. Preparation and Evaluation of Multi-Layer Anodes of Solid Oxide Fuel Cell

    Science.gov (United States)

    Santiago, Diana; Farmer, Serene C.; Setlock, John A.

    2012-01-01

    The development of an energy device with abundant energy generation, ultra-high specific power density, high stability and long life is critical for enabling longer missions and for reducing mission costs. Of all different types of fuel cells, the solid oxide fuel cells (SOFC) is a promising high temperature device that can generate electricity as a byproduct of a chemical reaction in a clean way and produce high quality heat that can be used for other purposes. For aerospace applications, a power-to-weight of (is) greater than 1.0 kW/kg is required. NASA has a patented fuel cell technology under development, capable of achieving the 1.0 kW/kg figure of merit. The first step toward achieving these goals is increasing anode durability. The catalyst plays an important role in the fuel cells for power generation, stability, efficiency and long life. Not only the anode composition, but its preparation and reduction are key to achieving better cell performance. In this research, multi-layer anodes were prepared varying the chemistry of each layer to optimize the performance of the cells. Microstructure analyses were done to the new anodes before and after fuel cell operation. The cells' durability and performance were evaluated in 200 hrs life tests in hydrogen at 850 C. The chemistry of the standard nickel anode was modified successfully reducing the anode degradation from 40% to 8.4% in 1000 hrs and retaining its microstructure.

  8. Fracture toughness of solid oxide fuel cell anode substrates determined by a double-torsion technique

    Science.gov (United States)

    Pećanac, G.; Wei, J.; Malzbender, J.

    2016-09-01

    Planar solid oxide fuel cell anode substrates are exposed to high mechanical loads during assembly, start-up, steady-state operation and thermal cycling. Hence, characterization of mechanical stability of anode substrates under different oxidation states and at relevant temperatures is essential to warrant a reliable operation of solid oxide fuel cells. As a basis for mechanical assessment of brittle supports, two most common anode substrate material variants, NiO-3YSZ and NiO-8YSZ, were analyzed in this study with respect to their fracture toughness at room temperature and at a typical stack operation temperature of 800 °C. The study considered both, oxidized and reduced materials' states, where also an outlook is given on the behavior of the re-oxidized state that might be induced by malfunctions of sealants or other functional components. Aiming at the improvement of material's production, different types of warm pressed and tape cast NiO-8YSZ substrates were characterized in oxidized and reduced states. Overall, the results confirmed superior fracture toughness of 3YSZ compared to 8YSZ based composites in the oxidized state, whereas in the reduced state 3YSZ based composites showed similar fracture toughness at room temperature, but a higher value at 800 °C compared to 8YSZ based composites. Complementary microstructural analysis aided the interpretation of mechanical characterization.

  9. Bacterial nanometric amorphous Fe-based oxide: a potential lithium-ion battery anode material.

    Science.gov (United States)

    Hashimoto, Hideki; Kobayashi, Genki; Sakuma, Ryo; Fujii, Tatsuo; Hayashi, Naoaki; Suzuki, Tomoko; Kanno, Ryoji; Takano, Mikio; Takada, Jun

    2014-04-23

    Amorphous Fe(3+)-based oxide nanoparticles produced by Leptothrix ochracea, aquatic bacteria living worldwide, show a potential as an Fe(3+)/Fe(0) conversion anode material for lithium-ion batteries. The presence of minor components, Si and P, in the original nanoparticles leads to a specific electrode architecture with Fe-based electrochemical centers embedded in a Si, P-based amorphous matrix.

  10. Fabrication, structural characterization and sensing properties of polydiacetylene nanofibers templated from anodized aluminum oxide

    Science.gov (United States)

    Polydiacetylene (PDA), a unique conjugated polymer, has shown its potential in the application of chem/bio-sensors and optoelectronics. In this work, we first infiltrated PDA monomer (10, 12-pentacosadiynoic acid, PCDA) melted into the anodized aluminum oxide template, and then illuminated the infil...

  11. Physical Properties of Mixed Conductor Solid Oxide Fuel Cell Anodes of Doped CeO2

    DEFF Research Database (Denmark)

    Mogensen, Mogens Bjerg; Lindegaard, Thomas; Hansen, Uffe Rud;

    1994-01-01

    conductivity vs. oxygen partial pressure. For both typesof conductivity a dependence on dopant valency was observed. The electronic conductivity was independent of dopantradius in contrast to the ionic which was highly dependent. These measured physical properties are compared with the idealrequirements...... for solid oxide fuel cell anodes. Not all requirements are fulfilled. Measures to compensate for this arediscussed....

  12. Effects of ultrasound on electrochemical oxidation mechanisms of p-substituted phenols at BDD and PbO2 anodes

    International Nuclear Information System (INIS)

    The effects of low-frequency (40 kHz) ultrasound are investigated with regard to the effectiveness and mechanisms of electrochemical oxidation of p-substituted phenols (p-nitrophenol, p-hydroxybenzaldehyde, phenol, p-cresol, and p-methoxyphenol) at BDD (boron-doped diamond) and PbO2 anodes. Although ultrasound improved the disappearance rates of p-substituted phenols at both the BDD and PbO2 anodes, the degree of enhancement varied according to the type of p-substituted phenol and type of anode under consideration. At the BDD anode, the %Increase values were in the range 73-83% for p-substituted phenol disappearance and in the range 60-70% for COD removal. However, at the PbO2 anode, the corresponding %Increase values were in the range 50-70% for disappearance of p-substituted phenols and only 5-25% for COD removal, much lower values than obtained at the BDD anode. Further investigations on the influence of ultrasound on the electrochemical oxidation mechanisms at BDD and PbO2 anodes revealed that the different increase extent were due to the specialized electrochemical oxidation mechanisms at these two anodes. The hydroxyl radicals were mainly free at the BDD electrodes with a larger reaction zone, but adsorbed at the PbO2 electrodes with a smaller reaction zone. Therefore, the enhancement due to ultrasound was greater at the BDD anode than at the PbO2 anode.

  13. Anodic oxidation of oxytetracycline: Influence of the experimental conditions on the degradation rate and mechanism

    Directory of Open Access Journals (Sweden)

    Annabel Fernandes

    2014-12-01

    Full Text Available The anodic oxidation of oxytetracycline was performed with success using as anode a boron-doped diamond electrode. The experiments were conducted in batch mode, using two different electrochemical cells: an up-flow cell, with recirculation, that was used to evaluate the influence of recirculation flow rate; and a stirred cell, used to determine the influence of the applied current density. Besides oxytetracyclin electrodegradation rate and mineralization extent, oxidation by-products were also assessed. Both the flow rate and the applied current density have shown positive influence on the oxytetracycline oxidation rate. On the other hand, the mineralization degree presented the highest values at the lowest flow rate and the lowest current density tested. The main oxidation by-products detected were oxalic, oxamic and maleic acids.

  14. Auto-inhibition effects in anodic oxidation of phenols for electrochemical waste-water purification

    OpenAIRE

    Conway, B. E.; H. AL-MAZNAI

    2001-01-01

    Removal or modification of noxious organic impurities in waste-waters is a major challenge for environmental science. Pollutants such as phenols and their derivatives, as well as PCBs, have attracted special attention. In recent years, the possibilities of effecting direct electrocatalytic oxidations at high-area electrodes such as supported Pt or RuO2 have been investigated. However, in a number of cases, especially with phenolic impurities, application of anodic oxidation fails to lead to c...

  15. Anodic destruction of abamectin acaricide solution by BDD-anodic oxidation

    OpenAIRE

    M. Errami; R. Salghi; Ebenso, Eno E.; Messali, M.; Al-Deyab, S.S.; B. Hammouti

    2014-01-01

    This paper presents the study of the electrochemical oxidation of the pesticide Abamectin at a boron-doped diamond (BDD). The effect of using different supporting electrolytes (NaCl, K2SO4, Na2CO3 and Na2SO4) during the galvanostatic electrolysis of Abamectin was investigated.The influence of several operating parameters, such as applied current density, effect of electrolytes (NaCl), was investigated. UV spectroscopy and chemical oxygen demand measurements were conducted t...

  16. Feed-forward control of a solid oxide fuel cell system with anode offgas recycle

    Science.gov (United States)

    Carré, Maxime; Brandenburger, Ralf; Friede, Wolfgang; Lapicque, François; Limbeck, Uwe; da Silva, Pedro

    2015-05-01

    In this work a combined heat and power unit (CHP unit) based on the solid oxide fuel cell (SOFC) technology is analysed. This unit has a special feature: the anode offgas is partially recycled to the anode inlet. Thus it is possible to increase the electrical efficiency and the system can be operated without external water feeding. A feed-forward control concept which allows secure operating conditions of the CHP unit as well as a maximization of its electrical efficiency is introduced and validated experimentally. The control algorithm requires a limited number of measurement values and few deterministic relations for its description.

  17. Salicylic acid electrooxidation. A surface film formation

    Energy Technology Data Exchange (ETDEWEB)

    Baturova, M.D.; Vedenjapin, A.; Baturova, M.M. [N.D. Zelinsky Inst. of Organic Chemistry, Russian Academy of Sciences, Moscow (Russian Federation); Weichgrebe, D.; Danilova, E.; Rosenwinkel, K.H. [Univ. of Hannover, Inst. of Water Quality and Waste Management Hannover (Germany); Skundin, A. [A.N. Frumkin Inst. of Electrochemistry, Russian Academy of Sciences, Moscow (Russian Federation)

    2003-07-01

    A possibility to use electrochemical treatment for salicylic acid (SA) removal from waste water was studied. It was found that SA can be oxidized at platinum anode with formation of harmless products. Features of anodic process, in particular, formation of solid film on anode surface as well as properties of the film were investigated. (orig.)

  18. Water clustering on nanostructured iron oxide films

    DEFF Research Database (Denmark)

    Merte, Lindsay Richard; Bechstein, Ralf; Peng, G.;

    2014-01-01

    , but it is not well-understood how these hydroxyl groups and their distribution on a surface affect the molecular-scale structure at the interface. Here we report a study of water clustering on a moire-structured iron oxide thin film with a controlled density of hydroxyl groups. While large amorphous monolayer...... islands form on the bare film, the hydroxylated iron oxide film acts as a hydrophilic nanotemplate, causing the formation of a regular array of ice-like hexameric nanoclusters. The formation of this ordered phase is localized at the nanometre scale; with increasing water coverage, ordered and amorphous...

  19. Anodic oxidation of o-nitrophenol on BDD electrode: Variable effects and mechanisms of degradation

    Energy Technology Data Exchange (ETDEWEB)

    Rabaaoui, Nejmeddine, E-mail: chimie_tunisie@yahoo.fr [Materials, Environment and Energy Laboratory (06/UR/12-01), Science Faculty of Gafsa, 2112, University of Gafsa (Tunisia); Saad, Mohamed El Khames [Materials, Environment and Energy Laboratory (06/UR/12-01), Science Faculty of Gafsa, 2112, University of Gafsa (Tunisia); Moussaoui, Younes [Materials, Environment and Energy Laboratory (06/UR/12-01), Science Faculty of Gafsa, 2112, University of Gafsa (Tunisia); Physical Organic Chemistry Laboratory, Science Faculty of Sfax, University of Sfax (Tunisia); Allagui, Mohamed Salah [Science Faculty of Gafsa, University of Gafsa (Tunisia); Bedoui, Ahmed [Materials, Environment and Energy Laboratory (06/UR/12-01), Science Faculty of Gafsa, 2112, University of Gafsa (Tunisia); Science Faculty of Gabes, 6072, University of Gabes (Tunisia); Elaloui, Elimame [Materials, Environment and Energy Laboratory (06/UR/12-01), Science Faculty of Gafsa, 2112, University of Gafsa (Tunisia); Science Faculty of Gafsa, University of Gafsa (Tunisia)

    2013-04-15

    Highlights: ► Anodic oxidation is an effective method for degrading o-nitrophenol. ► The effect of operating parameters on the degradation was investigated. ► The main intermediate products were determined by HPLC technique. ► A plausible degradation pathway of o-nitrophenol was proposed. -- Abstract: The electrochemical oxidation of pesticide, o-nitrophenol (ONP) as one kind of pesticide that is potentially dangerous and biorefractory, was studied by galvanostatic electrolysis using boron-doped diamond (BDD) as anode. The influence of several operating parameters, such as applied current density, supporting electrolyte, and initial pH value, was investigated. The best degradation occurred in the presence of Na{sub 2}SO{sub 4} (0.05 M) as conductive electrolyte. After 8 h, nearly complete degradation of o-nitrophenol was achieved (92%) using BDD electrodes at pH 3 and at current density equals 60 mA cm{sup −2}. The decay kinetics of o-nitrophenol follows a pseudo-first-order reaction. Aromatic intermediates such as catechol, resorcinol, 1,2,4-trihydroxybenzene, hydroquinone and benzoquinone and carboxylic acids such as maleic glycolic, malonic, glyoxilic and oxalic, have been identified and followed during the ONP treatment by chromatographic techniques. From these anodic oxidation by-products, a plausible reaction sequence for ONP mineralization on BDD anodes is proposed.

  20. Numerical modeling of the failure mechanisms in silicon thin film anode for lithium-ion batteries

    Science.gov (United States)

    Patel, Siddharth H.

    2011-12-01

    In recent times, the demand for the storage of electrical energy has grown rapidly for both static applications and the portable electronics enforcing the substantial improvement in battery systems, and Li-ion batteries have been proven to have maximum energy storage density in all rechargeable batteries. However, major breakthroughs are required to consummate the requirement of higher energy density with lower cost to penetrate new markets. Graphite anode having limited capacity has become a bottle neck in the process of developing next generation batteries and can be replaced by higher capacity metals such as Silicon. In the present study we are focusing on the mechanical behavior of the Si-thin film anode under various operating conditions. A numerical model is developed to simulate the intercalation induced stress and the failure mechanism of the complex anode structure. Effect of the various physical phenomena such as diffusion induced stress, plasticity and the crack propagation are investigated to predict better performance parameters for improved design.

  1. Oxide films in high temperature aqueous environments

    International Nuclear Information System (INIS)

    The evaluation of modified water chemistries as well as of the effects of increased power output in nuclear power plants is associated with a need to understand their effect on occupational dose rates and on environmentally assisted cracking as well as other types of corrosion of structural materials. Occupational dose rates are due to activity build-up on the primary circuit components, which in turn depends on the dissolution, transport, deposition and incorporation of the activated corrosion products in the oxide films formed on material surfaces. Accordingly, activity build-up is influenced by the electrochemical and electric properties of the oxide films and by the water chemistry of the coolant. Concerning different types of corrosion, it can with good reason be assumed that both the oxidation reaction related to corrosion (e.g. crack growth) as well as the coupled cathodic reaction involve steps in which charged species are transported through the oxide films formed on material surfaces either within the crack or on surfaces exposed to the bulk coolant. It can also be stated that a sufficient characterisation and a satisfactory model for the electrochemical behaviour and electric properties of the oxide films formed in nuclear power plants are not available. More experimental support is needed concerning especially the preferential paths and driving forces for ion transport as well as the nature of mobile species or defects. The lack of sufficient understanding has complicated the assessment of the applicability and possible side-effects of e.g. noble metal water chemistry and the injection of zinc as a means to prevent the uptake of activated corrosion products into corrosion films. The long-term aim of the work performed within the present research program is to minimise the risk of activity build-up, environmentally assisted cracking (EAC) and other types of corrosion, as well as to be prepared for the evaluation and introduction of modified water

  2. In Situ Carbonized Cellulose-Based Hybrid Film as Flexible Paper Anode for Lithium-Ion Batteries.

    Science.gov (United States)

    Cao, Shaomei; Feng, Xin; Song, Yuanyuan; Liu, Hongjiang; Miao, Miao; Fang, Jianhui; Shi, Liyi

    2016-01-20

    Flexible free-standing carbonized cellulose-based hybrid film is integrately designed and served both as paper anode and as lightweight current collector for lithium-ion batteries. The well-supported heterogeneous nanoarchitecture is constructed from Li4Ti5O12 (LTO), carbonized cellulose nanofiber (C-CNF) and carbon nanotubes (CNTs) using by a pressured extrusion papermaking method followed by in situ carbonization under argon atmospheres. The in situ carbonization of CNF/CNT hybrid film immobilized with uniform-dispersed LTO results in a dramatic improvement in the electrical conductivity and specific surface area, so that the carbonized paper anode exhibits extraordinary rate and cycling performance compared to the paper anode without carbonization. The flexible, lightweight, single-layer cellulose-based hybrid films after carbonization can be utilized as promising electrode materials for high-performance, low-cost, and environmentally friendly lithium-ion batteries. PMID:26727586

  3. Microstructural evolution of tungsten oxide thin films

    Science.gov (United States)

    Hembram, K. P. S. S.; Thomas, Rajesh; Rao, G. Mohan

    2009-10-01

    Tungsten oxide thin films are of great interest due to their promising applications in various optoelectronic thin film devices. We have investigated the microstructural evolution of tungsten oxide thin films grown by DC magnetron sputtering on silicon substrate. The structural characterization and surface morphology were carried out using X-ray diffraction and Scanning Electron Microscopy (SEM). The as deposited films were amorphous, where as, the films annealed above 400 °C were crystalline. In order to explain the microstructural changes due to annealing, we have proposed a "instability wheel" model for the evolution of the microstructure. This model explains the transformation of mater into various geometries within them selves, followed by external perturbation.

  4. Microstructural evolution of tungsten oxide thin films

    Energy Technology Data Exchange (ETDEWEB)

    Hembram, K.P.S.S., E-mail: hembram@isu.iisc.ernet.in [Department of Instrumentation, Indian Institute of Science, Bangalore - 560 012 (India); Theoretical Science Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Jakkur, Bangalore - 560064 (India); Thomas, Rajesh; Rao, G. Mohan [Department of Instrumentation, Indian Institute of Science, Bangalore - 560 012 (India)

    2009-10-30

    Tungsten oxide thin films are of great interest due to their promising applications in various optoelectronic thin film devices. We have investigated the microstructural evolution of tungsten oxide thin films grown by DC magnetron sputtering on silicon substrate. The structural characterization and surface morphology were carried out using X-ray diffraction and Scanning Electron Microscopy (SEM). The as deposited films were amorphous, where as, the films annealed above 400 deg. were crystalline. In order to explain the microstructural changes due to annealing, we have proposed a 'instability wheel' model for the evolution of the microstructure. This model explains the transformation of mater into various geometries within them selves, followed by external perturbation.

  5. Reduced Graphene Oxide/Tin-Antimony Nanocomposites as Anode Materials for Advanced Sodium-Ion Batteries.

    Science.gov (United States)

    Ji, Liwen; Zhou, Weidong; Chabot, Victor; Yu, Aiping; Xiao, Xingcheng

    2015-11-11

    Reduced graphene oxides loaded with tin-antimony alloy (RGO-SnSb) nanocomposites were synthesized through a hydrothermal reaction and the subsequent thermal reduction treatments. Transmission electron microscope images confirm that SnSb nanoparticles with an average size of about 20-30 nm are uniformly dispersed on the RGO surfaces. When they were used as anodes for rechargeable sodium (Na)-ion batteries, these as-synthesized RGO-SnSb nanocomposite anodes delivered a high initial reversible capacity of 407 mAh g(-1), stable cyclic retention for more than 80 cycles and excellent cycle stability at ultra high charge/discharge rates up to 30C. The significantly improved performance of the synthesized RGO-SnSb nanocomposites as Na-ion battery anodes can be attributed to the synergetic effects of RGO-based flexible framework and the nanoscale dimension of the SnSb alloy particles (batteries.

  6. Optimization of dry reforming of methane over Ni/YSZ anodes for solid oxide fuel cells

    Science.gov (United States)

    Guerra, Cosimo; Lanzini, Andrea; Leone, Pierluigi; Santarelli, Massimo; Brandon, Nigel P.

    2014-01-01

    This work investigates the catalytic properties of Ni/YSZ anodes as electrodes of Solid Oxide Fuel Cells (SOFCs) to be operated under direct dry reforming of methane. The experimental test rig consists of a micro-reactor, where anode samples are characterized. The gas composition at the reactor outlet is monitored using a mass spectrometer. The kinetics of the reactions occurring over the anode is investigated by means of Isotherm reactions and Temperature-programmed reactions. The effect of the variation of temperature, gas residence time and inlet carbon dioxide-methane volumetric ratio is analyzed. At 800 °C, the best catalytic performance (in the carbon safe region) is obtained for 1.5 reactions, respectively. In other ranges, dry reforming and reverse water gas shift are the dominant reactions and the inlet feed reaches almost the equilibrium condition provided that a sufficient gas residence time is obtained.

  7. Preparation via an electrochemical method of graphene films coated on both sides with NiO nanoparticles for use as high-performance lithium ion anodes

    International Nuclear Information System (INIS)

    We report on a simple strategy for the direct synthesis of a thin film comprising interconnected NiO nanoparticles deposited on both sides of a graphene sheet via cathodic deposition. For the co-electrodeposition, graphene oxide (GO) is treated with water-soluble cationic poly(ethyleneimine) (PEI) which acts as a stabilizer and trapping agent to form complexes of GO and Ni2+. The positively charged complexes migrate toward the stainless steel substrate, resulting in the electrochemical deposition of PEI-modified GO/Ni(OH)2 at the electrode surface under an applied electric field. The as-synthesized film is then converted to graphene/NiO after annealing at 350 ° C. The interconnected NiO nanoparticles are uniformly deposited on both sides of the graphene surface, as evidenced by field emission scanning electron microscopy, transmission electron microscopy and energy dispersive spectrometry. This graphene/NiO structure shows enhanced electrochemical performance with a large reversible capacity, good cyclic performance and improved electronic conductivity as an anode material for lithium ion batteries. A reversible capacity is retained above 586 mA h g−1 after 50 cycles. The findings reported herein suggest that this strategy can be effectively used to overcome a bottleneck problem associated with the electrochemical production of graphene/metal oxide films for lithium ion battery anodes. (paper)

  8. Mineralization of bisphenol A (BPA) by anodic oxidation with boron-doped diamond (BDD) electrode

    Energy Technology Data Exchange (ETDEWEB)

    Murugananthan, M. [Satellite Venture Business Laboratory, Utsunomiya University, 7-1-2 Yoto, Utsunomiya, Tochigi 321-8585 (Japan)], E-mail: muruga.chem@gmail.com; Yoshihara, S. [Department of Energy and Environmental Science, Graduate School of Engineering, Utsunomiya University, 7-1-2 Yoto, Utsunomiya, Tochigi 321-8585 (Japan)], E-mail: sachioy@cc.utsunomiya-u.ac.jp; Rakuma, T.; Shirakashi, T. [Department of Energy and Environmental Science, Graduate School of Engineering, Utsunomiya University, 7-1-2 Yoto, Utsunomiya, Tochigi 321-8585 (Japan)

    2008-06-15

    Anodic oxidation of bisphenol A (BPA), a representative endocrine disrupting chemical, was carried out using boron-doped diamond (BDD) electrode at galvanostatic mode. The electro-oxidation behavior of BPA at BDD electrode was investigated by means of cyclic voltammetric technique. The extent of degradation and mineralization of BPA were monitored by HPLC and total organic carbon (TOC) value, respectively. The results obtained, indicate that the BPA removal at BDD depends on the applied current density (I{sub appl}), initial concentration of BPA, pH of electrolyte and supporting medium. Galvanostatic electrolysis at BDD anode cause concomitant generation of hydroxyl radical that leads to the BPA destruction. The kinetics for the BPA degradation follows a pseudo-first order reaction with a higher rate constant 12.8 x 10{sup -5} s{sup -1} for higher I{sub appl} value 35.7 mA cm{sup -2}, indicating that the oxidation reaction is limited by I{sub appl} control. Complete mineralization of BPA was achieved regardless of the variables and accordingly the mineralization current efficiency was calculated from the TOC removal measurements. Considering global oxidation process, the effect of supporting electrolytes has been discussed in terms of the electro generated inorganic oxidants. The better performance of BDD anode was proved on a comparative study with Pt and glassy carbon under similar experimental conditions. A possible reaction mechanism for BPA degradation involving three main aromatic intermediates, identified by GC-MS analysis, was proposed.

  9. Mineralization of bisphenol A (BPA) by anodic oxidation with boron-doped diamond (BDD) electrode

    International Nuclear Information System (INIS)

    Anodic oxidation of bisphenol A (BPA), a representative endocrine disrupting chemical, was carried out using boron-doped diamond (BDD) electrode at galvanostatic mode. The electro-oxidation behavior of BPA at BDD electrode was investigated by means of cyclic voltammetric technique. The extent of degradation and mineralization of BPA were monitored by HPLC and total organic carbon (TOC) value, respectively. The results obtained, indicate that the BPA removal at BDD depends on the applied current density (Iappl), initial concentration of BPA, pH of electrolyte and supporting medium. Galvanostatic electrolysis at BDD anode cause concomitant generation of hydroxyl radical that leads to the BPA destruction. The kinetics for the BPA degradation follows a pseudo-first order reaction with a higher rate constant 12.8 x 10-5 s-1 for higher Iappl value 35.7 mA cm-2, indicating that the oxidation reaction is limited by Iappl control. Complete mineralization of BPA was achieved regardless of the variables and accordingly the mineralization current efficiency was calculated from the TOC removal measurements. Considering global oxidation process, the effect of supporting electrolytes has been discussed in terms of the electro generated inorganic oxidants. The better performance of BDD anode was proved on a comparative study with Pt and glassy carbon under similar experimental conditions. A possible reaction mechanism for BPA degradation involving three main aromatic intermediates, identified by GC-MS analysis, was proposed

  10. Light-Weight Free-Standing Carbon Nanotube-Silicon Films for Anodes of Lithium Ion Batteries

    KAUST Repository

    Cui, Li-Feng

    2010-07-27

    Silicon is an attractive alloy-type anode material because of its highest known capacity (4200 mAh/g). However, lithium insertion into and extraction from silicon are accompanied by a huge volume change, up to 300%, which induces a strong strain on silicon and causes pulverization and rapid capacity fading due to the loss of the electrical contact between part of silicon and current collector. Si nanostructures such as nanowires, which are chemically and electrically bonded to the current collector, can overcome the pulverization problem, however, the heavy metal current collectors in these systems are larger in weight than Si active material. Herein we report a novel anode structure free of heavy metal current collectors by integrating a flexible, conductive carbon nanotube (CNT) network into a Si anode. The composite film is free-standing and has a structure similar to the steel bar reinforced concrete, where the infiltrated CNT network functions as both mechanical support and electrical conductor and Si as a high capacity anode material for Li-ion battery. Such free-standing film has a low sheet resistance of ∼30 Ohm/sq. It shows a high specific charge storage capacity (∼2000 mAh/g) and a good cycling life, superior to pure sputtered-on silicon films with similar thicknesses. Scanning electron micrographs show that Si is still connected by the CNT network even when small breaking or cracks appear in the film after cycling. The film can also "ripple up" to release the strain of a large volume change during lithium intercalation. The conductive composite film can function as both anode active material and current collector. It offers ∼10 times improvement in specific capacity compared with widely used graphite/copper anode sheets. © 2010 American Chemical Society.

  11. Light-weight free-standing carbon nanotube-silicon films for anodes of lithium ion batteries.

    Science.gov (United States)

    Cui, Li-Feng; Hu, Liangbing; Choi, Jang Wook; Cui, Yi

    2010-07-27

    Silicon is an attractive alloy-type anode material because of its highest known capacity (4200 mAh/g). However, lithium insertion into and extraction from silicon are accompanied by a huge volume change, up to 300%, which induces a strong strain on silicon and causes pulverization and rapid capacity fading due to the loss of the electrical contact between part of silicon and current collector. Si nanostructures such as nanowires, which are chemically and electrically bonded to the current collector, can overcome the pulverization problem, however, the heavy metal current collectors in these systems are larger in weight than Si active material. Herein we report a novel anode structure free of heavy metal current collectors by integrating a flexible, conductive carbon nanotube (CNT) network into a Si anode. The composite film is free-standing and has a structure similar to the steel bar reinforced concrete, where the infiltrated CNT network functions as both mechanical support and electrical conductor and Si as a high capacity anode material for Li-ion battery. Such free-standing film has a low sheet resistance of approximately 30 Ohm/sq. It shows a high specific charge storage capacity (approximately 2000 mAh/g) and a good cycling life, superior to pure sputtered-on silicon films with similar thicknesses. Scanning electron micrographs show that Si is still connected by the CNT network even when small breaking or cracks appear in the film after cycling. The film can also "ripple up" to release the strain of a large volume change during lithium intercalation. The conductive composite film can function as both anode active material and current collector. It offers approximately 10 times improvement in specific capacity compared with widely used graphite/copper anode sheets. PMID:20518567

  12. Microstructure, mechanical and electrical properties of Ni-YSZ anode supported solid oxide fuel cells

    Directory of Open Access Journals (Sweden)

    G. Matula

    2008-07-01

    Full Text Available Purpose: Investigation of the Ni-YSZ cermets for anode supported solid oxide fuel cells (SOFC prepared byuniaxial pressure, sintered and reduced pellets of NiO-YSZ.Design/methodology/approach: Density examination, shrinkage examination, transverse rupture strengthtests, microstructure examination.Findings: Basing on the investigations of the anode Ni-YSZ type fabricated with powder metallurgy it wasfound of that density of sintered samples depends on NiO portion, temperature of sintering and reducing. Increaseof sintering temperature causes increase of density. Moreover increase of NiO portion and reducing temperaturecauses decrease of density and linear contraction of anode.Practical implications: The Ni-YSZ cermets fabricated using of powder metallurgy are characterized by verygood properties and can be used as SOFC anode. Powder metallurgy gives the possibility to manufacturing cermetused as an anode for SOFC on the basis of Ni-YSZ.Originality/value: Investigations of compacted, sintered and reduced samples with different amount of NiOgives information about optimal manufacturing conditions and volume fraction of NiO/YSZ components. Thisinformation is especially important at production process of extruded tubes.

  13. Layered reduced graphene oxide with nanoscale interlayer gaps as a stable host for lithium metal anodes

    Science.gov (United States)

    Lin, Dingchang; Liu, Yayuan; Liang, Zheng; Lee, Hyun-Wook; Sun, Jie; Wang, Haotian; Yan, Kai; Xie, Jin; Cui, Yi

    2016-07-01

    Metallic lithium is a promising anode candidate for future high-energy-density lithium batteries. It is a light-weight material, and has the highest theoretical capacity (3,860 mAh g–1) and the lowest electrochemical potential of all candidates. There are, however, at least three major hurdles before lithium metal anodes can become a viable technology: uneven and dendritic lithium deposition, unstable solid electrolyte interphase and almost infinite relative dimension change during cycling. Previous research has tackled the first two issues, but the last is still mostly unsolved. Here we report a composite lithium metal anode that exhibits low dimension variation (∼20%) during cycling and good mechanical flexibility. The anode is composed of 7 wt% ‘lithiophilic’ layered reduced graphene oxide with nanoscale gaps that can host metallic lithium. The anode retains up to ∼3,390 mAh g–1 of capacity, exhibits low overpotential (∼80 mV at 3 mA cm–2) and a flat voltage profile in a carbonate electrolyte. A full-cell battery with a LiCoO2 cathode shows good rate capability and flat voltage profiles.

  14. Layered reduced graphene oxide with nanoscale interlayer gaps as a stable host for lithium metal anodes

    Science.gov (United States)

    Lin, Dingchang; Liu, Yayuan; Liang, Zheng; Lee, Hyun-Wook; Sun, Jie; Wang, Haotian; Yan, Kai; Xie, Jin; Cui, Yi

    2016-07-01

    Metallic lithium is a promising anode candidate for future high-energy-density lithium batteries. It is a light-weight material, and has the highest theoretical capacity (3,860 mAh g-1) and the lowest electrochemical potential of all candidates. There are, however, at least three major hurdles before lithium metal anodes can become a viable technology: uneven and dendritic lithium deposition, unstable solid electrolyte interphase and almost infinite relative dimension change during cycling. Previous research has tackled the first two issues, but the last is still mostly unsolved. Here we report a composite lithium metal anode that exhibits low dimension variation (˜20%) during cycling and good mechanical flexibility. The anode is composed of 7 wt% ‘lithiophilic’ layered reduced graphene oxide with nanoscale gaps that can host metallic lithium. The anode retains up to ˜3,390 mAh g-1 of capacity, exhibits low overpotential (˜80 mV at 3 mA cm-2) and a flat voltage profile in a carbonate electrolyte. A full-cell battery with a LiCoO2 cathode shows good rate capability and flat voltage profiles.

  15. Large Scale Inert Anode for Molten Oxide Electrolysis Project

    Data.gov (United States)

    National Aeronautics and Space Administration — Molten oxide electrolysis is a demonstrated laboratory-scale process for producing oxygen from the JSC-1a lunar simulant; however, critical subsystems necessary for...

  16. Metal oxide films on glass and steel substrates

    International Nuclear Information System (INIS)

    A variety of thin (10-1000nm) metal oxide films have been deposited on flat glass substrates by the pyrolysis of an aerosol of metal acetylacetonates in a suitable carrier. The optical characteristics and thickness of the films have been measured and particular interest has centered on the use of a novel pin on disc apparatus to measure the physical durability of such thin films. Characteristic friction/penetration force traces have been established for 1st Series transition metal oxide films and some ranking in terms of 'hardness' established. The use of SnO2 - coated glass for electrodes in a light modulator cell has been examined. The electrochromic behaviour of a silver matrix in DMSO electrolyte has been observed in a small glass cell and by cyclic voltammetry on a vitreous carbon electrode. Optimum conditions for practical light-shutter have been established and electrode processes elucidated. A corrosion study of mild steel in two different water/organic electrolytes of industrial importance has been carried out. Mechanisms to account for the corrosion observed have been presented. Support for the usual anodic reaction is presented Fe → Fe2+ + 2e but in the electrolyte operated at low pH film formation of a water soluble organic 'tar' has been confirmed and the proposed reaction Fe2+ + H2O → FeOH+ + H+ leads to a local increase in [H+] which accounts for the observed corrosion rate. In contrast, corrosion behaviour in the pH8 electrolyte supports the view that the rate limiting reduction reaction is possibly oxygen (or water) reduction although some contribution from an organic 'impurity' cannot be ruled out. Coatings of Fe3O4 on mild steel have been prepared by CVD using pneumatic spraying techniques and the corrosion behaviour of coated electrodes in organic-phosphate electrolyte (pH8) has been examined. (author)

  17. A photoemission study of the effectiveness of nickel, manganese, and cobalt based corrosion barriers for silicon photo-anodes during water oxidation

    Science.gov (United States)

    O'Connor, Robert; Bogan, Justin; McCoy, Anthony; Byrne, Conor; Hughes, Greg

    2016-05-01

    Silicon is an attractive material for solar water splitting applications due to its abundance and its capacity to absorb a large fraction of incident solar radiation. However, it has not received as much attention as other materials due to its tendency to oxidize very quickly in aqueous environments, particularly when it is employed as the anode where it drives the oxygen evolution reaction. In recent years, several works have appeared in the literature examining the suitability of thin transition metal oxide films grown on top of the silicon to act as a corrosion barrier. The film should be transparent to solar radiation, allow hole transport from the silicon surface to the electrolyte, and stop the diffusion of oxygen from the electrolyte back to the silicon. In this work, we compare Mn-oxide, Co-oxide, and Ni-oxide thin films grown using physical vapor deposition in order to evaluate which material offers the best combination of photocurrent and corrosion protection. In addition to the electrochemical data, we also present a detailed before-and-after study of the surface chemistry of the films using x-ray photoelectron spectroscopy. This approach allows for a comprehensive analysis of the mechanisms by which the corrosion barriers protect the underlying silicon, and how they degrade during the water oxidation reaction.

  18. Electrochemical Characteristics of Tin Oxide-Graphite as Anode Material for Lithium-ion Cells

    Science.gov (United States)

    Hasanaly, Siti Munirah

    2010-03-01

    Tin oxide anode materials used in lithium-ion cells experience large volume changes during charging and discharging which cause substantial losses in capacity. In this work, the tin oxide-graphite composite is proposed as an alternative anode material to overcome this problem. The composite was synthesised from a solution of tin chloride dihydrate and graphite powders with citric acid as the chelating agent. In this sol-gel method, a solid phase is formed through a chemical reaction in a liquid phase at moderate temperature. The technique offers several advantages compared to the solid state synthesis technique such as the ability to maintain the homogeneous mixture of precursors during synthesis and to produce small particles. The electrochemical behaviour of the anode material was investigated by means of galvanostatic charge discharge technique. An initial reversible capacity of 748 mAh/g is obtained and nearly 600 mAh/g was retained upon the reaching the fifth cycle. This study shows that the presence of graphite is able to minimise the agglomeration of tin particles that causes large volume changes during cycling, thereby improving cyclability of the anode material.

  19. Electrochemical oxidation of polyethylene glycol in electroplating solution using paraffin composite copper hexacyanoferrate modified (PCCHM) anode

    Institute of Scientific and Technical Information of China (English)

    Rajesh S. Bejankiwar; Abir Basu; Max Cementi

    2004-01-01

    Electrochemical oxidation of polyethylene glycol(PEG) in an acidic(pH 0.18 to 0.42) and high ionic strength electroplating solution was investigated. The electroplating solution is a major source of wastewater in the printing wiring board industry. A paraffin composite copper hexacyanoferrate modified(PCCHM) electrode was used as the anode and a bare graphite electrode was used as the cathode. The changes in PEG and total organic carbon(TOC) concentrations during the course of the reaction were monitored. The efficiency of the PCCHM anode was compared with bare graphite anode and it was found that the former showed significant electrocatalytic property for PEG and TOC removal. Chlorides present in the solution were found to contribute significantly in the overall organic removal process. Short chain organic compounds like acetic acid, oxalic acid, formic acid and ethylene glycol formed during electrolysis were identified by HPLC method. Anode surface area and applied current density were found to influence the electro-oxidation process, in which the former was found to be dominating. Investigations of the kinetics for the present electrochemical reaction suggested that the two stage first-order kinetic model provides a much better representation of the overall mechanism of the process if compared to the generalized kinetic model.

  20. Facile synthesis of multilayer-like Si thin film as high-performance anode materials for lithium-ion batteries

    Science.gov (United States)

    Wang, Mingxu; Geng, Zhongrong

    2016-05-01

    For the silicon anodes in lithium-ion batteries, it is well known that the enormous volumetric expansion/contraction is also the mainly reason for the capacity fading. In this manuscript, a new kind of Si thin films was prepared with a radio frequency magnetron sputtering method. By using a periodic modulation negative bias on the substrate, a density-modulated multilayer-like silicon thin films with different layer densities were used as anode materials of lithium-ion batteries, and which displayed a high capacity and stable cycling performances. The reason for the charming electrochemical performances may be owned to the particular density modulated microstructure of the Si thin films. It is conjectured that the lower density can as compliant layers and which provided the volume for the higher-density layer expansion in the process of the lithiation/delithiation. In contrast to the conventional silicon anodes, the density modulated microstructure in this work could exploit a new approach to silicon thin-film anode materials with outstanding electrochemical properties and mechanical stability. And these reports may be provide a new way to prepare the Si thin films for the high-energy, safe, and low-cost batteries.

  1. The contribution of mediated oxidation mechanisms in the electrolytic degradation of cyanuric acid using diamond anodes.

    Science.gov (United States)

    Bensalah, Nasr; Dbira, Sondos; Bedoui, Ahmed

    2016-07-01

    In this work, the contribution of mediated oxidation mechanisms in the electrolytic degradation of cyanuric acid using boron-doped diamond (BDD) anodes was investigated in different electrolytes. A complete mineralization of cyanuric acid was obtained in NaCl; however lower degrees of mineralization of 70% and 40% were obtained in Na2SO4 and NaClO4, respectively. This can be explained by the nature of the oxidants electrogenerated in each electrolyte. It is clear that the contribution of active chlorine (Cl2, HClO, ClO(-)) electrogenerated from oxidation of chlorides on BDD is much more important in the electrolytic degradation of cyanuric acid than the persulfate and hydroxyl radicals produced by electro-oxidation of sulfate and water on BDD anodes. This could be explained by the high affinity of active chlorine towards nitrogen compounds. No organic intermediates were detected during the electrolytic degradation of cyanuric acid in any the electrolytes, which can be explained by their immediate depletion by hydroxyl radicals produced on the BDD surface. Nitrates and ammonium were the final products of electrolytic degradation of cyanuric acid on BDD anodes in all electrolytes. In addition, small amounts of chloramines were formed in the chloride medium. Low current density (≤10mA/cm(2)) and neutral medium (pH in the range 6-9) should be used for high efficiency electrolytic degradation and negligible formation of hazardous chlorate and perchlorate. PMID:27372125

  2. Electrochemically induced oxidative removal of As(III) from groundwater in a dual-anode sand column.

    Science.gov (United States)

    Tong, Man; Yuan, Songhu; Wang, Zimeng; Luo, Mingsen; Wang, Yanxin

    2016-03-15

    In situ treatment of high-arsenic groundwater cost-effectively is still challenging. We proposed an in situ treatment approach which utilizes O2 produced from groundwater electrolysis to increase the redox potential for oxidative removal of arsenic. A sand column was configured to simulate groundwater flow in an aquifer, and a stable anode, a stable cathode and an iron anode were arrayed in an upward mode in the column to evaluate the performance on arsenic removal from the groundwater induced by the oxidative precipitation of Fe(2+) by O2. As(III) at 500μg/L was efficiently oxidized to As(V) by the stable anode followed by the reactive oxidants produced from Fe(II)-O2, and total As were completely removed by the newly formed amorphous iron hydroxides. Quantitative models for the dependence of As(III) oxidation, total As removal and Fe(II) oxidative precipitation on the flow rate and the current density applied to Fe anode were developed. The presence of humic substance promoted the oxidation of As(III) on the stable anode but inhibited the oxidation and removal induced by Fe(II) oxidative precipitation. A stable performance on As(III) oxidation and removal was observed in a 10-day continuous operation. Results from this study prove that groundwater electrolysis could be applicable for oxidative removal of As(III) in porous media, with a controllable and lasting treatment efficiency. PMID:26642445

  3. The effect of porosity gradient in a Nickel/Yttria Stabilized Zirconia anode for an anode-supported planar solid oxide fuel cell

    Energy Technology Data Exchange (ETDEWEB)

    An, Chung Min; Sammes, Nigel [Department of Metallurgical and Materials Engineering, Colorado School of Mines, Golden, CO (United States); Song, Jung-Hoon [RIST, Pohang (Korea); Kang, Inyong [Department of Chemical Engineering, Colorado School of Mines, Golden, CO (United States)

    2010-02-01

    In this paper, a graded Ni/YSZ cermet anode, an 8 mol.%YSZ electrolyte, and a lanthanum strontium manganite (LSM) cathode were used to fabricate a solid oxide fuel cell (SOFC) unit. An anode-supported cell was prepared using a tape casting technique followed by hot pressing lamination and a single step co-firing process, allowing for the creation of a thin layer of dense electrolyte on a porous anode support. To reduce activation and concentration overpotential in the unit cell, a porosity gradient was developed in the anode using different percentages of pore former to a number of different tape-slurries, followed by tape casting and lamination of the tapes. The unit cell demonstrated that a concentration distribution of porosity in the anode increases the power in the unit cell from 76 mW cm{sup -2} to 101 mW cm{sup -2} at 600 C in humidified hydrogen. Although the results have not been optimized for good performance, the effect of the porosity gradient is quite apparent and has potential in developing superior anode systems. (author)

  4. Scale-up of B-doped diamond anode system for electrochemical oxidation of phenol simulated wastewater in batch mode

    Energy Technology Data Exchange (ETDEWEB)

    Zhu Xiuping [Department of Environmental Engineering, Peking University, Key Laboratory of Water and Sediment Sciences, Ministry of Education, Beijing 100871 (China); Ni Jinren, E-mail: nijinren@iee.pku.edu.cn [Department of Environmental Engineering, Peking University, Key Laboratory of Water and Sediment Sciences, Ministry of Education, Beijing 100871 (China); Wei Junjun; Chen Pan [Department of Environmental Engineering, Peking University, Key Laboratory of Water and Sediment Sciences, Ministry of Education, Beijing 100871 (China)

    2011-10-30

    Scale-up of boron-doped diamond (BDD) anode system is critical to the practical application of electrochemical oxidation in bio-refractory organic wastewater treatment. In this study, the scale-up of BDD anode system was investigated on batch-mode electrochemical oxidation of phenol simulated wastewater. It was demonstrated that BDD anode system was successfully scaled up by 121 times without performance deterioration based on the COD and specific energy consumption (E{sub sp}) models in bath mode. The COD removal rate and E{sub sp} for the scaled-up BDD anode system through enlarging the total anode area while keeping similar configuration, remained at the similar level as those before being scaled up, under the same area/volume value, current density, retention time and wastewater characteristics. The COD and E{sub sp} models used to describe the smaller BDD anode system satisfactorily predicted the performance of the scaled-up BDD anode system. Under the suitable operating conditions, the COD of phenol simulated wastewater was reduced from 540 mg l{sup -1} to 130 mg l{sup -1} within 3 h with an E{sub sp} of only 34.76 kWh m{sup -3} in the scaled-up BDD anode system. These results demonstrate that BDD anode system is very promising in practical bio-refractory organic wastewater treatment.

  5. Dependence of Performance of Organic Light-emitting Devices on Sheet Resistance of Indium-tin-oxide Anodes

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    The dependence of the performance of organic light-emitting devices(OLEDs) on the sheet resistance of indium-tin-oxide(ITO) anodes was investigated by measuring the steady state current density brightness voltage characteristics and the electroluminescent spectra. The device with a higher sheet resistance anode shows a lower current density, a lower brightness level, and a higher operation voltage. The electroluminescence(EL) efficiencies of the devices with the same structure but different ITO anodes show more complicated differences. Furthermore, the shift of the light-emitting zone toward the anode was found when an anode with a higher sheet resistance was used. These performance differences are discussed and attributed to the reduction of hole injection and the increase in voltage drop over ITO anode with the increase in sheet resistance.

  6. Optical Properties of Au Nanoparticles Coated on Surface of Glass or Anodic Aluminum Oxide Template

    Institute of Scientific and Technical Information of China (English)

    FENG Jinyang; WU Can; MA Xiao; ZHANG Hongquan; ZHAO Xiujian

    2012-01-01

    Au nanoparticles coated on the surface of glass (Sample A) or on anodic aluminum oxide template surface (Sample B) were prepared using titanium dioxide sol-gel doped with chloroauric acid and with a reduction process.FE-SEM,UV-Vis spectrum and Fluorescence spectrum tests show that Au nanoparticles have been distributed randomly on the surface of glass,while deposition occurs on the surface of regular hollows for anodic aluminum oxide template.A sharp absorption peak appears at the wavelength of 536 nm for sample B,while there is a red shift,with a broader peak for sample A.A distinct fluorescence emission at the wavelength of 633 nm is detected for sample A,but no noticeable fluorescence emission has been found for Sample B.The results indicate that the microstructure and optical properties of Au nanoparticles can be modulated by different substrate.

  7. A solid oxide fuel cell with a gadolinia-doped ceria anode: Preparation and performance

    DEFF Research Database (Denmark)

    Marina, O.A.; Bagger, C.; Primdahl, S.;

    1999-01-01

    The application of doped ceria as an anode material in high-temperature solid oxide fuel cells (SOFC) is described. Deposition of an anchoring layer of YSZ particles was used to obtain sufficient adhesion between a porous Ce0.6Gd0.4O1.8 (CG4) anode and an yrttria-stabilised zirconia (YSZ...... internal resistance of 0.39 Ohm cm(2) at 0.71 V cell voltage and a power density of 470 mW/cm(2) was obtained at 1000 degrees C using H-2/H2O/N-2 = 9/1.2/89.8 as the fuel and air as oxidant. A current density of 0.25 A/cm(2) at an area specific internal resistance of 2 Ohm cm(2) was obtained with CH4/H2O...

  8. Bioactive titanium metal surfaces with antimicrobial properties prepared by anodic oxidation treatment

    Institute of Scientific and Technical Information of China (English)

    YUE ChongXia; YANG BangCheng; ZHANG XingDong

    2009-01-01

    In order to endow titanium metals with bioactivity and antimicrobial properties,titanium plates were subjected to anodic oxidation treatment in NaCI solutions in this study.The treated titanium metals could induce apatite formation in the fast calcification solution,and osteoblasts on the treated titanium surfaces proliferated well as those on the untreated titanium metal surfaces.The treated metals could inhibit S.aureus growth in the microbial culture experiments.It was assumed that Ti-OH groups and Ti-CI groups formed on the treated titanium surface were responsible for the bioactivity and antimicrobial properties of the metals.The anodic oxidation treatment was an effective way to prepare bioactive titanium surfaces with antimicrobial properties.

  9. Bioactive titanium metal surfaces with antimicrobial properties prepared by anodic oxidation treatment

    Institute of Scientific and Technical Information of China (English)

    2009-01-01

    In order to endow titanium metals with bioactivity and antimicrobial properties, titanium plates were subjected to anodic oxidation treatment in NaCl solutions in this study. The treated titanium metals could induce apatite formation in the fast calcification solution, and osteoblasts on the treated titanium surfaces proliferated well as those on the untreated titanium metal surfaces. The treated metals could inhibit S. aureus growth in the microbial culture experiments. It was assumed that Ti-OH groups and Ti-Cl groups formed on the treated titanium surface were responsible for the bioactivity and antimicrobial properties of the metals. The anodic oxidation treatment was an effective way to prepare bioactive titanium surfaces with antimicrobial properties.

  10. A mixed proton-oxide ion-electron conducting anode for highly coking-resistant solid oxide fuel cells

    International Nuclear Information System (INIS)

    Highlights: • A multi-phase mixed proton-oxide ion-electron conducting anode was employed. • BaO/Ni interfaces facilitate water-mediated carbon removal. • Fast oxygen ions flux and formed water are favorable for hydrocarbon reformation. - Abstract: A multi-phase mixed proton-oxide ion-electron conducting composite is employed as a new anode material for a coking-resistant solid oxide fuel cell (SOFC) based on oxide ion conducting electrolyte, operated in methane and ethanol. The formation of BaO/Ni interfaces can effectively readily adsorb water and facilitate water-mediated carbon removal. The fast oxygen ions flux and formed steam at anode side are also found to be favorable for hydrocarbon reformation to promote the cell performance and long term stability. At 700 °C, maximum power densities of 580 and 368 mW cm−2 are achieved in methane and ethanol, respectively. The resistance against carbon deposition is significantly improved, showing stable voltage in 120 h durability test

  11. Transformation and removal of arsenic in groundwater by sequential anodic oxidation and electrocoagulation

    Science.gov (United States)

    Zhang, Peng; Tong, Man; Yuan, Songhu; Liao, Peng

    2014-08-01

    Oxidation of As(III) to As(V) is generally essential for the efficient remediation of As(III)-contaminated groundwater. The performance and mechanisms of As(III) oxidation by an as-synthesized active anode, SnO2 loaded onto Ti-based TiO2 nanotubes (Ti/TiO2NTs/Sb-SnO2), were investigated. The subsequent removal of total arsenic by electrocoagulation (EC) was further tested. The Ti/TiO2NTs/Sb-SnO2 anode showed a high and lasting electrochemical activity for As(III) oxidation. 6.67 μM As(III) in synthetic groundwater was completely oxidized to As(V) within 60 min at 50 mA. Direct electron transfer was mainly responsible at the current below 30 mA, while hydroxyl radicals contributed increasingly with the increase in the current above 30 mA. As(III) oxidation was moderately inhibited by the presence of bicarbonate (20 mM), while was dramatically increased with increasing the concentration of chloride (0-10 mM). After the complete oxidation of As(III) to As(V), total arsenic was efficiently removed by EC in the same reactor by reversing electrode polarity. The removal efficiency increased with increasing the current but decreased by the presence of phosphate and silica. Anodic oxidation represents an effective pretreatment approach to increasing EC removal of As(III) in groundwater under O2-limited conditions.

  12. Polymer Photovoltaic Cells with Rhenium Oxide as Anode Interlayer.

    Directory of Open Access Journals (Sweden)

    Jinyu Wei

    Full Text Available The effect of a new transition metal oxide, rhenium oxide (ReO3, on the performance of polymer solar cells based on regioregular poly(3-hexylthiophene (P3HT and methanofullerene [6,6]-phenyl C61-butyric acid methyl ester (PCBM blend as buffer layer was investigated. The effect of the thickness of ReO3 layer on electrical characteristics of the polymer solar cells was studied. It is found that insertion of ReO3 interfacial layer results in the decreased performance for P3HT: PCBM based solar cells. In order to further explore the mechanism of the decreasing of the open-circuit voltage (Voc, the X-ray photoelectron spectroscopy (XPS is used to investigate the ReO3 oxidation states. Kelvin Probe method showed that the work function of the ReO3 is estimated to be 5.13eV after thermal evaporation. The results indicated the fact that a portion of ReO3 decomposed during thermal evaporation process, resulting in the formation of a buffer layer with a lower work function. As a consequence, a higher energy barrier was generated between the ITO and the active layer.

  13. The cooperative electrochemical oxidation of chlorophenols in anode-cathode compartments

    Energy Technology Data Exchange (ETDEWEB)

    Wang Hui [Laboratory of Environmental Technology, INET, Tsinghua University, Beijing 100084 (China); Wang Jianlong [Laboratory of Environmental Technology, INET, Tsinghua University, Beijing 100084 (China)], E-mail: wangjl@tsinghua.edu.cn

    2008-06-15

    By using a self-made carbon/polytetrafluoroethylene (C/PTFE) O{sub 2}-fed as the cathode and Ti/IrO{sub 2}/RuO{sub 2} as the anode, the degradation of three organic compounds (phenol, 4-chlorophenol, and 2,4-dichlorophenol) was investigated in the diaphragm (with terylene as diaphragm material) electrolysis device by electrochemical oxidation process. The result indicated that the concentration of hydrogen peroxide (H{sub 2}O{sub 2}) was 8.3 mg/L, and hydroxyl radical (HO{center_dot}) was determined in the cathodic compartment by electron spin resonance spectrum (ESR). The removal efficiency for organic compounds reached about 90% after 120 min, conforming to the sequence of phenol, 4-chlorophenol, and 2,4-dichlorophenol. And the dechlorination degree of 4-chlorophenol exceeded 90% after 80 min. For H{sub 2}O{sub 2}, HO{center_dot} existed in the catholyte and reduction dechlorination at the cathode, the mineralization of organics in the cathodic compartment was better than that in the anodic compartment. The degradation of organics was supposed to be cooperative oxidation by direct or indirect electrochemical oxidation at the anode and H{sub 2}O{sub 2}, HO{center_dot} produced by oxygen reduction at the cathode. High-performance liquid chromatography (HPLC) allowed identifying phenol as the dechlorination product of 4-chlorophenol in the cathodic compartment, and hydroquinone, 4-chlorocatechol, benzoquinone, maleic, fumaric, oxalic, and formic acids as the main oxidation intermediates in the cathodic and anodic compartments. A reaction scheme involving all these intermediates was proposed.

  14. Electrochemical Oxidation Using BDD Anodes Combined with Biological Aerated Filter for Biotreated Coking Wastewater Treatment

    OpenAIRE

    Wang, C.R.; Hou, Z. F.; M. R. Zhang; J. Qi; Wang, J.

    2015-01-01

    Coking wastewater is characterized by poor biodegradability and high microorganism toxicity. Thus, it is difficult to meet Grade I of Integrated Wastewater Discharge Standard of China by biological treatment technology; specifically, COD cannot meet above standard due to containing refractory organics. A novel coupling reactor, electrochemical oxidation using BDD anodes and biological aerated filter (BAF), has been developed for carbon and nitrogen removal from biotreated coking wastewater, f...

  15. Electrodeposition of cerium oxide on porous silicon via anodization and enhancement of photoluminescence

    Science.gov (United States)

    Mizuhata, Minoru; Kubo, Yohei; Maki, Hideshi

    2016-02-01

    A porous Si/cerium oxide composite (PSi/CeO2) was synthesized by electrodeposition of CeO2 via anodic oxidation on PSi. The PSi photoluminescence (PL) was enhanced. The anodically oxidized PSi substrates in HF solution had macropores (diameter 2 μm), mesopores (diameter 15 nm), and micropores (diameter less than 4 nm). Emission at 700 nm from microporous PSi (microPSi) was observed under ultraviolet irradiation. Transmission electron microscopy showed that in microPSi/CeO2, the oxide was infiltrated into microPSi by anodization. The deposited amount of CeO2 depended on the reaction time, applied voltage, temperature, and reaction species concentrations in anodization. Emission by microPSi/CeO2 at 650 nm was observed; the PL intensity was higher (about 10-30 times) than that of PSi because of energy transfer from CeO2 to nanosized Si in porous layers produced by HF etching. The lifetime of the PL of microPSi/CeO2 was longer than that of microPSi. Excitation spectra of microPSi/CeO2 at 650 nm and diffuse-reflectance spectra showed that the excitation peak for microPSi/CeO2 was similar to the absorbance of CeO2, and excitation of microPSi/CeO2 gave two peaks, at 3.7 and 4.4 eV; these peaks originated from the absorptions of CeO2 and Si nanocrystals. The PL of PSi was enhanced in microPSi/CeO2 because of efficient energy transfer from CeO2 to the Si nanocrystal.

  16. Graphene oxide film as solid lubricant.

    Science.gov (United States)

    Liang, Hongyu; Bu, Yongfeng; Zhang, Junyan; Cao, Zhongyue; Liang, Aimin

    2013-07-10

    As a layered material, graphene oxide (GO) film is a good candidate for improving friction and antiwear performance of silicon-based MEMS devices. Via a green electrophoretic deposition (EPD) approach, GO films with tunable thickness in nanoscale are fabricated onto silicon wafer in a water solution. The morphology, microstructure, and mechanical properties as well as the friction coefficient and wear resistance of the films were investigated. The results indicated that the friction coefficient of silicon wafer was reduced to 1/6 its value, and the wear volume was reduced to 1/24 when using GO film as solid lubricant. These distinguished tribology performances suggest that GO films are expected to be good solid lubricants for silicon-based MEMS/NEMS devices. PMID:23786494

  17. Photo-electrochemical Oxidation of Organic C1 Molecules over WO3 Films in Aqueous Electrolyte: Competition Between Water Oxidation and C1 Oxidation.

    Science.gov (United States)

    Reichert, Robert; Zambrzycki, Christian; Jusys, Zenonas; Behm, R Jürgen

    2015-11-01

    To better understand organic-molecule-assisted photo-electrochemical water splitting, photo-electrochemistry and on-line mass spectrometry measurements are used to investigate the photo-electrochemical oxidation of the C1 molecules methanol, formaldehyde, and formic acid over WO3 film anodes in aqueous solution and its competition with O2 evolution from water oxidation O2 (+) and CO2 (+) ion currents show that water oxidation is strongly suppressed by the organic species. Photo-electro-oxidation of formic acid is dominated by formation of CO2 , whereas incomplete oxidation of formaldehyde and methanol prevails, with the selectivity for CO2 formation increasing with increasing potential and light intensity. The mechanistic implications for the photo-electro-oxidation of the organic molecules and its competition with water oxidation, which could be derived from this novel approach, are discussed.

  18. Photo-electrochemical Oxidation of Organic C1 Molecules over WO3 Films in Aqueous Electrolyte: Competition Between Water Oxidation and C1 Oxidation.

    Science.gov (United States)

    Reichert, Robert; Zambrzycki, Christian; Jusys, Zenonas; Behm, R Jürgen

    2015-11-01

    To better understand organic-molecule-assisted photo-electrochemical water splitting, photo-electrochemistry and on-line mass spectrometry measurements are used to investigate the photo-electrochemical oxidation of the C1 molecules methanol, formaldehyde, and formic acid over WO3 film anodes in aqueous solution and its competition with O2 evolution from water oxidation O2 (+) and CO2 (+) ion currents show that water oxidation is strongly suppressed by the organic species. Photo-electro-oxidation of formic acid is dominated by formation of CO2 , whereas incomplete oxidation of formaldehyde and methanol prevails, with the selectivity for CO2 formation increasing with increasing potential and light intensity. The mechanistic implications for the photo-electro-oxidation of the organic molecules and its competition with water oxidation, which could be derived from this novel approach, are discussed. PMID:26382643

  19. Growth characterization of anodic film on AZ91D magnesium alloy in an electrolyte of Na2SiO3 and KF

    Institute of Scientific and Technical Information of China (English)

    Weiping Li; Liqun Zhu; Yihong Li; Bo Zhao

    2006-01-01

    Anodization of AZ91D magnesium alloy in the electrolyte solution of 0.5 mol/L of sodium silicate and 1.0 mol/L of potassium fluoride was investigated. The anodic films were characterized using optical microscopy (OM), scanning electron microscopy (SEM), and X-ray diffraction (XRD). The corrosion resistance of the various anodized alloys was evaluated by a fast corrosion test using the solution of hydrochloric acid and potassium dichromate. The results showed that the addition of KF resulted in the presence of NaF in the anodic film. The thickness of the anodic film formed under a constant current density of 20 mA/cm2 for 16 min at 60℃ exceeded 100 μm. The growth of the anodic film could be divided into three stages based on the anodizing time; the growth rate was much faster during stage Ⅱ than in stages Ⅰ and Ⅲ. The anodic film exhibited the highest corrosion resistance for the AZ91 alloy,which is attributed to the fact that the anodization was maintained until the end of stage Ⅱ.

  20. Aluminum oxide as a dual-functional modifier of Ni-based anodes of solid oxide fuel cells for operation on simulated biogas

    Science.gov (United States)

    Wang, Feng; Wang, Wei; Ran, Ran; Tade, Moses O.; Shao, Zongping

    2014-12-01

    Al2O3 and SnO2 additives are introduced into the Ni-YSZ cermet anode of solid oxide fuel cells (SOFCs) for operation on simulated biogas. The effects of incorporating Al2O3/SnO2 on the electrical conductivity, morphology, coking resistance and catalytic activity for biogas reforming of the cermet anode are systematically studied. The electrochemical performance of the internal reforming SOFC is enhanced by introducing an appropriate amount of Al2O3 into the anode, but it becomes worse with excess alumina addition. For SnO2, a negative effect on the electrochemical performance is demonstrated, although the coking resistance of the anode is improved. For fuel cells operating on biogas, stable operation under a polarization current for 130 h at 750 °C is achieved for a cell with an Al2O3-modified anode, while cells with unmodified or SnO2-modified Ni-YSZ anodes show much poorer stability under the same conditions. The improved performance of the cell with the Al2O3-modified anode mainly results from the suppressed coking and sintering of the anode and from the formation of NiAl2O4 in the unreduced anode. In sum, modifying the anode with Al2O3 may be a useful and facile way to improve the coking resistance and electrochemical performance of the nickel-based cermet anodes for SOFCs.

  1. ANODIC STRIPPING VOLTAMMETRY AT A MERCURY FILM ELECTRODE: BASELINE CONCENTRATIONS OF CADMIUM, LEAD, AND COPPER IN SELECTED NATURAL WATERS

    Science.gov (United States)

    A simple, rapid, and inexpensive anodic stripping voltammetric method with a mercury thin film electrode is reported for the establishment of baseline concentrations of cadmium, lead, and copper in natural waters. The procedure for routine surface preparation of wax-impregnated g...

  2. Olive mill wastewater treatment by anodic oxidation with parallel plate electrodes.

    Science.gov (United States)

    Panizza, Marco; Cerisola, Giacomo

    2006-03-01

    Olive mill wastewater is characterized by very high chemical oxygen demand (COD) values and contains high concentrations of polyphenols that inhibit the activity of micro-organisms during biological oxidations. In this paper, the applicability of electrochemical oxidation of a real olive-mill wastewater was studied by performing galvanostatic electrolysis using parallel plate electrodes. A mixed titanium and ruthenium oxide (Ti/TiRuO2) was used as anode and stainless steel as cathode. The effect of chloride concentration and applied current on the removal of COD, aromatic content and colour was investigated. The experimental results showed that an effective electrochemical oxidation was achieved in which the wastewater was decolourised and the COD and aromatic content completely eliminated. In particular, the mineralisation took place by indirect oxidation, mediated by active chlorine, and the COD removal rate was enhanced by the addition of 5 g L(-1) of NaCl to the wastewater and by increasing the applied current. PMID:16510168

  3. An artificial photosynthesis anode electrode composed of a nanoparticulate photocatalyst film in a visible light responsive GaN-ZnO solid solution system

    Science.gov (United States)

    Imanaka, Yoshihiko; Anazawa, Toshihisa; Manabe, Toshio; Amada, Hideyuki; Ido, Sachio; Kumasaka, Fumiaki; Awaji, Naoki; Sánchez-Santolino, Gabriel; Ishikawa, Ryo; Ikuhara, Yuichi

    2016-01-01

    The artificial photosynthesis technology known as the Honda-Fujishima effect, which produces oxygen and hydrogen or organic energy from sunlight, water, and carbon dioxide, is an effective energy and environmental technology. The key component for the higher efficiency of this reaction system is the anode electrode, generally composed of a photocatalyst formed on a glass substrate from electrically conductive fluorine-doped tin oxide (FTO). To obtain a highly efficient electrode, a dense film composed of a nanoparticulate visible light responsive photocatalyst that usually has a complicated multi-element composition needs to be deposited and adhered onto the FTO. In this study, we discovered a method for controlling the electronic structure of a film by controlling the aerosol-type nanoparticle deposition (NPD) condition and thereby forming films of materials with a band gap smaller than that of the prepared raw material powder, and we succeeded in extracting a higher current from the anode electrode. As a result, we confirmed that a current approximately 100 times larger than those produced by conventional processes could be obtained using the same material. This effect can be expected not only from the materials discussed (GaN-ZnO) in this paper but also from any photocatalyst, particularly materials of solid solution compositions. PMID:27759108

  4. Oxidation of H2 and CO in a fuel cell with a Platinum-tin Anode

    Directory of Open Access Journals (Sweden)

    Javier González

    2010-06-01

    Full Text Available This report describes the construction and evolution of a fuel cell with a bi-metallic anode of Pt-Sn supported on carbon, as catalysts for oxidation of pure hydrogen, pure CO and a 2% CO in H2 mixture. Both, cathode and anode were made with a structure composed by a diffusive layer and a catalytic layer. The diffusive layer was made with a carbon cloth while the catalytic layer contained the platinum and tin supported on carbon. To test the performance of the catalytic mixture, a proton exchange membrane fuel cell (PEMFC was developed with an original design for the gas distributation plates. The reactants were feed to ambient temperature and 3 psig in the anode side, while 5 psig pure oxygen was used in the cathode. The anode catalytic load was 0.57 mg/cm2 of platinum and 0.08 mg/cm2 of tin. The catalytic load in cathode was 0.85 mg/cm2 of pure platinum. It was found that this caralytic mixture is tolerant to CO presence.

  5. Highly durable anode supported solid oxide fuel cell with an infiltrated cathode

    DEFF Research Database (Denmark)

    Samson, Alfred Junio; Hjalmarsson, Per; Søgaard, Martin;

    2012-01-01

    An anode supported solid oxide fuel cell with an La0.6Sr0.4Co1.05O3_δ (LSC) infiltrated-Ce0.9Gd0.1O1.95 (CGO) cathode that shows a stable performance has been developed. The cathode was prepared by screen printing a porous CGO backbone on top of a laminated and co-fired anode supported half cell......, consisting of a Nieyttria stabilized zirconia (YSZ) anode support, a Niescandia-doped yttria-stabilized zirconia (ScYSZ) anode, a ScYSZ electrolyte, and a CGO barrier layer. LSC was introduced into the CGO backbone by multiple infiltrations of an aqueous nitrate solution followed by firing. The cell...... in the resistance from the recorded impedance was observed during long term testing. The power density reached 0.79Wcm-2 at a cell voltage of 0.6 V at 750 deg. C. Post test analysis of the LSC infiltrated-CGO cathode by scanning electron microscopy revealed no significant micro-structural difference...

  6. Photoelectrode thin film of dye-sensitized solar cell fabricated by anodizing method and spin coating and electrochemical impedance properties of DSSC

    Energy Technology Data Exchange (ETDEWEB)

    Chang, Ho, E-mail: f10381@ntut.edu.tw [Graduate Institute of Manufacturing Technology, National Taipei University of Technology, Taipei 10608, Taiwan (China); Chen, Chih-Hao [Department of Thoracic Surgery, Mackay Memorial Hospital, Taipei 10419, Taiwan (China); Graduate Institute of Mechanical and Electrical Engineering, National Taipei University of Technology, Taipei 10608, Taiwan (China); Kao, Mu-Jung [Department of Vehicle Engineering, National Taipei University of Technology, Taipei 10608, Taiwan (China); Chien, Shu-Hua [Institute of Chemistry, Academia Sinica, Taipei 115, Taiwan (China); Chou, Cheng-Yi [Graduate Institute of Manufacturing Technology, National Taipei University of Technology, Taipei 10608, Taiwan (China)

    2013-06-15

    The paper studies the photoelectrode thin film of dye-sensitized solar cell (DSSC) fabricated by anodizing method, explores the structure and properties of the fabricated photoelectrode thin film, measures the photoelectric conversion efficiency of DSSC, and finds the electrochemical impedance properties of DSSCs assembled by photoelectrode thin films in different thicknesses. Besides, in order to increase the specific surface area of nanotubes, this paper deposits TiO{sub 2} nanoparticles (TNP) on the surface of titanium oxide nanotube (TNT). As shown in experimental results, the photoelectric conversion efficiency of the DSSC fabricated by the study rises to 6.5% from the original 5.43% without TnB treatment, with an increase of photoelectric conversion efficiency by 19.7%. In addition, when the photoelectrode thin film is fabricated with mixture of TNTs and TNP in an optimal proportion of 2:8 and the photoelectrode thin film thickness is 15.5 μm, the photoelectric conversion efficiency can reach 7.4%, with an increase of 36.7% from the original photoelectric conversion efficiency at 5.43%. Besides, as found in the results of electrochemical impedance analysis, the DSSC with photoelectrode thin film thickness at 15.5 μm has the lowest charge-conduction resistance (R{sub k}) value 9.276 Ω of recombined electron and conduction resistance (R{sub w}) value 3.25 Ω of electrons in TiO{sub 2}.

  7. Stable solar-driven oxidation of water by semiconducting photoanodes protected by transparent catalytic nickel oxide films

    KAUST Repository

    Sun, Ke

    2015-03-11

    Reactively sputtered nickel oxide (NiOx) films provide transparent, antireflective, electrically conductive, chemically stable coatings that also are highly active electrocatalysts for the oxidation of water to O2(g). These NiOx coatings provide protective layers on a variety of technologically important semiconducting photoanodes, including textured crystalline Si passivated by amorphous silicon, crystalline n-type cadmium telluride, and hydrogenated amorphous silicon. Under anodic operation in 1.0 M aqueous potassium hydroxide (pH 14) in the presence of simulated sunlight, the NiOx films stabilized all of these self-passivating, high-efficiency semiconducting photoelectrodes for >100 h of sustained, quantitative solar-driven oxidation of water to O2(g). © 2015, National Academy of Sciences. All rights reserved.

  8. Facile Synthesis of Porous-Structured Nickel Oxide Thin Film by Pulsed Laser Deposition

    Directory of Open Access Journals (Sweden)

    Siamak Pilban Jahromi

    2012-01-01

    Full Text Available Porous-structured nickel oxide (PsNiO was obtained through the oxidization of a nickel thin film. The nickel thin film was deposited using the pulsed laser deposition (PLD method on a nickel foil as a substrate. The results show uniform PsNiO after the oxidization of the nickel thin film at 750∘C for 1 h. X-ray diffraction (XRD indicates formation of the NiO crystalline structure. Field emission scanning electron microscopy (FESEM reveals different morphology on the surface of the nickel foil (sample A and on the nickel thin film (sample B. Comparison of the FESEM results after oxidization shows that the PsNiO on the nickel thin film was more regular and controllable than the NiO layer on the nickel foil. The FESEM images also show that the thickness of the nickel thin film affected the PsNiO size obtained after oxidization. This resulted from the growth of the porous structure at grain boundaries and from the grain sizes. The electrochemical properties of the PsNiO as an electrode are investigated by cyclic voltammetry (CV. These results show the effect of PsNiO size on the current of anodic peak.

  9. Monitoring Volumetric Changes in Silicon Thin-Film Anodes through In Situ Optical Diffraction Microscopy.

    Science.gov (United States)

    Duay, Jonathon; Schroder, Kjell W; Murugesan, Sankaran; Stevenson, Keith J

    2016-07-13

    A high-resolution in situ spectroelectrochemical optical diffraction experiment has been developed to understand the volume expansion/contraction process of amorphous silicon (a-Si) thin-film anodes. Electrodes consisting of 1D transmissive gratings of silicon have been produced through photolithographic methods. After glovebox assembly in a home-built Teflon cell, monitoring of the diffraction efficiency of these gratings during the lithiation/delithiation process is performed using an optical microscope equipped with a Bertrand lens. When the diffraction efficiency along with optical constants obtained from in situ spectroscopic ellipsometry is utilized, volume changes of the active materials can be deduced. Unlike transmission electron microscopy and atomic force microscopy characterization methods of observing silicon's volume expansion, this experiment allows for real-time monitoring of the volume change at charge/discharge cycles greater than just the first few along with an experimental environment that directly mimics that of a real battery. This technique shows promising results that provide needed insight into understanding the lithium alloying reaction and subsequent induced capacity fade during the cycling of alloying anodes in lithium-ion batteries. PMID:27311132

  10. High quality transparent conducting oxide thin films

    Science.gov (United States)

    Gessert, Timothy A.; Duenow, Joel N.; Barnes, Teresa; Coutts, Timothy J.

    2012-08-28

    A transparent conducting oxide (TCO) film comprising: a TCO layer, and dopants selected from the elements consisting of Vanadium, Molybdenum, Tantalum, Niobium, Antimony, Titanium, Zirconium, and Hafnium, wherein the elements are n-type dopants; and wherein the transparent conducting oxide is characterized by an improved electron mobility of about 42 cm.sup.2/V-sec while simultaneously maintaining a high carrier density of .about.4.4e.times.10.sup.20 cm.sup.-3.

  11. Nanosegregated bimetallic oxide anode catalyst for proton exchange membrane electrolyzer

    Energy Technology Data Exchange (ETDEWEB)

    Danilovic, Nemanja; Kang, Yijin; Markovic, Nenad; Stamenkovic, Vojislav; Myers, Deborah J.; Subbaraman, Ram

    2016-08-23

    A surface segregated bimetallic composition of the formula Ru.sub.1-xIr.sub.x wherein 0.1.ltoreq.x.ltoreq.0.75, wherein a surface of the material has an Ir concentration that is greater than an Ir concentration of the material as a whole is provided. The surface segregated material may be produced by a method including heating a bimetallic composition of the formula Ru.sub.1-xIr.sub.x, wherein 0.1.ltoreq.x.ltoreq.0.75, at a first temperature in a reducing environment, and heating the composition at a second temperature in an oxidizing environment. The surface segregated material may be utilized in electrochemical devices.

  12. Fabrication of CoPd alloy nanowire arrays on an anodic aluminum oxide/Ti/Si substrate and their enhanced magnetic properties

    International Nuclear Information System (INIS)

    An anodic aluminum oxide/Ti/Si substrate was successfully synthesized by the anodization of an aluminum film on a Ti/Si substrate and then used as a template to grow 10 nm diameter CoPd alloy nanowires. X-ray diffraction and energy-dispersed X-ray patterns indicated that Co0.97Pd0.03 nanowire arrays with a preferential orientation of (0 0 2) were formed during electrodeposition. High coercivity (about 1700 Oe) and squareness (about 0.85) were obtained in the samples when the magnetic field was applied parallel to the axis of the nanowires; these values are much larger than those of pure Co nanowire arrays with the same diameters

  13. Synthesis by anodic-spark deposition of Ca- and P-containing films on pure titanium and their biological response

    Science.gov (United States)

    Banakh, Oksana; Journot, Tony; Gay, Pierre-Antoine; Matthey, Joël; Csefalvay, Catherine; Kalinichenko, Oleg; Sereda, Olha; Moussa, Mira; Durual, Stéphane; Snizhko, Lyubov

    2016-08-01

    The purpose of this work is to characterize the anodized layers formed on titanium by anodic-spark deposition in an electrolyte containing Ca and P ions, Ca3(PO4)2, studied for the first time. The oxidation experiments were performed at different periods of time and using different concentrations of electrolyte. The influence of the process parameters (time of electrolysis and electrolyte concentration) on the surface morphology and chemical composition of the anodized layers was studied. It has been found that it is possible to incorporate Ca and P into the growing layer. A response of the anodized layers in a biological medium was evaluated by their immersion in a simulated body fluid. An enrichment of titanium and a simultaneous loss of calcium and phosphorus in the layer after immersion tests indicate that these coatings should be bioresorbable in a biological medium. Preliminary biological assays were performed on some anodized layers in order to assess their biocompatibility with osteoblast cells. The cell proliferation on one selected anodized sample was assessed up to 21 days after seeding. The preliminary results suggest excellent biocompatibility properties of anodized coatings.

  14. Electrochemical Oxidation of Ammonia on Ir Anode in Potential Fixed Electrochemical Sensor

    Institute of Scientific and Technical Information of China (English)

    HAN Yi-ping; LUO Peng; CAI Chen-xin; XIE Lei; LU Tian-hong

    2008-01-01

    Ir catalyst possesses a good electrocatalytic activity and selectivity for the oxidation of NH3 and/or NH4OH at Ir anode in the potential fixed electrochemical sensor with the neutral solution.Owing to the same electrochemical behavior of NH3 and NH4OH in a NaCIO4 solution,NH4OH can be used instead of NH3 for the experimental convenience.It was found that the potential of the oxidation peak of NH4OH at the Ir/GC electrode in NaCIO4 solutions is at about 0.85 V,and the current density of the oxidation peak of NH4OH is linearly proportional to the concentration of NH4OH.The electrocatalytic oxidation of NH4OH is diffusion-controlled.Especially,Ir has no electrocatalytic activity for the CO oxidation,illustrating that CO does not interfere in the measurement of NH4OH and the potential fixed electrochemical NH3 sensor with the neutral solution,and the anodic Ir catalyst possesses a good selectivity.Therefore,lr may have practical application in the potential fixed electrochemical NH3 sensor with the neutral solution.

  15. Graphite coated with manganese oxide/multiwall carbon nanotubes composites as anodes in marine benthic microbial fuel cells

    Energy Technology Data Exchange (ETDEWEB)

    Fu, Yubin, E-mail: ffyybb@ouc.edu.cn; Yu, Jian; Zhang, Yelong; Meng, Yao

    2014-10-30

    Highlights: • MnO{sub 2}/MWCNTs composites anode exhibits faster reaction kinetics. • The surfaces of MnO{sub 2}/MWCNTs composites anode exhibits better wettability. • A BMFC using the modified anode have excellent power output. - Abstract: Improving anode performance is of great significance to scale up benthic microbial fuel cells (BMFCs) for its marine application to drive oceanography instruments. In this study, manganese oxide (MnO{sub 2})/multiwall carbon nanotubes (MWCNTs) composites are prepared to be as novel anodes in the BMFCs via a direct redox reaction between permanganate ions (MnO{sub 4}{sup −}) and MWCNTs. The results indicate that the MnO{sub 2}/MWCNTs anode has a better wettability, greater kinetic activity and higher power density than that of the plain graphite (PG) anode. It is noted that the MnO{sub 2} (50% weight percent)/MWCNTs anode shows the highest electrochemical performance among them and will be a promising material for improving bioelectricity production of the BMFCs. Finally, a synergistic mechanism of electron transfer shuttle of Mn ions and their redox reactions in the interface between modified anode and bacteria biofilm are proposed to explain its excellent electrochemical performance.

  16. Transition metal oxide-carbon composites as conversion anodes for sodium-ion battery

    International Nuclear Information System (INIS)

    Herein, we characterize various metal oxide-carbon composites, i.e. CuO-MCMB (mesocarbon microbeads), Fe2O3–MCMB and NiO-MCMB, as anode materials for application in sodium-ion battery. The electrodes, supposed to react through a conversion mechanism, are studied in terms of structure, morphology and electrochemical behavior in sodium cell. The results demonstrate a specific capacity of the order of 100 mAh g−1 for Fe2O3–MCMB and NiO-MCMB, and of about 300 mAh g−1 for CuO-MCMB. The remarkable performance of the latter suggests the copper oxide-based electrode as the preferred anode material for battery application. Indeed, further study aimed to clarify the Na/CuO-MCMB reaction mechanism is performed by ex-situ X-ray diffraction on electrode material cast onto aluminum support. The study suggests a partial conversion reaction for CuO-based anode that is considered suitable candidate in replacement of sodium metal, in efficient and safe Na-ion battery

  17. OBTENTION OF POROUS TITANIUM DIOXIDE COATINGS BY ANODIC OXIDATION FOR PHOTOCATALYTIC APPLICATIONS

    Directory of Open Access Journals (Sweden)

    Hernán D. Traid

    2016-03-01

    Full Text Available Titanium dioxide is one of the most used materials in heterogeneous photocatalysis process due its low cost, low toxicity and high photocatalytic activity. In the present work, porous TiO2 coatings are obtained by anodic oxidation, starting at constant current density and continuing at constant potential of 120 V in spark discharge conditions. After the oxidation, the coatings received a thermal treatment. The studied variable was the current density. The curves of current density and potential showed characteristics fluctuations of spark discharge. Micrographs of the oxides showed an average pore diameter of 100 nm. Diffractograms showed, in all cases, the presence of the anatase and rutile phases of TiO2, showing an increase of the rutile fraction when the current density was higher. The synthesized oxides showed favorable characteristics as potential materials for heterogeneous catalysis processes for water treatment.

  18. Auto-inhibition effects in anodic oxidation of phenols for electrochemical waste-water purification

    Directory of Open Access Journals (Sweden)

    B. E. CONWAY

    2001-12-01

    Full Text Available Removal or modification of noxious organic impurities in waste-waters is a major challenge for environmental science. Pollutants such as phenols and their derivatives, as well as PCBs, have attracted special attention. In recent years, the possibilities of effecting direct electrocatalytic oxidations at high-area electrodes such as supported Pt or RuO2 have been investigated. However, in a number of cases, especially with phenolic impurities, application of anodic oxidation fails to lead to continuous Faradaic oxidation currents owing to the electrode surfaces becoming blocked with polymeric oxidation products leading to auto-inhibition (“passivation” of the desired electrode process. Examples of such effects with phenols and related compounds are examined comparatively in the present paper by means of cyclic volatammetry and chronoamperometry.

  19. Rational design of metal oxide nanocomposite anodes for advanced lithium ion batteries

    Science.gov (United States)

    Li, Yong; Yu, Shenglan; Yuan, Tianzhi; Yan, Mi; Jiang, Yinzhu

    2015-05-01

    Metal-oxide anodes represent a significant future direction for advanced lithium ion batteries. However, their practical applications are still seriously hampered by electrode disintegration and capacity fading during cycling. Here, we report a rational design of 3D-staggered metal-oxide nanocomposite electrode directly fabricated by pulsed spray evaporation chemical vapor deposition, where various oxide nanocomponents are in a staggered distribution uniformly along three dimensions and across the whole electrode. Such a special design of nanoarchitecture combines the advantages of nanoscale materials in volume change and Li+/electron conduction as well as uniformly staggered and compact structure in atom migration during lithiation/delithiation, which exhibits high specific capacity, good cycling stability and excellent rate capability. The rational design of metal-oxide nanocomposite electrode opens up new possibilities for high performance lithium ion batteries.

  20. Effect of annealing on photoluminescence and optical properties of porous anodic alumina films formed in sulfuric acid for solar energy applications

    Energy Technology Data Exchange (ETDEWEB)

    Ghrib, Mondher, E-mail: mondherghrib@yahoo.fr [Photovoltaic Laboratory Research and Technology Centre of Energy, Borj-Cedria Science and Technology Park, BP 95, 2050 Hammam-Lif (Tunisia); Ouertani, Rachid, E-mail: rachid.ouertani@crten.rnrt.tn [Photovoltaic Laboratory Research and Technology Centre of Energy, Borj-Cedria Science and Technology Park, BP 95, 2050 Hammam-Lif (Tunisia); Gaidi, Monir; Khedher, Najoua [Photovoltaic Laboratory Research and Technology Centre of Energy, Borj-Cedria Science and Technology Park, BP 95, 2050 Hammam-Lif (Tunisia); Salem, Mohamed Ben [L3M, Department of Physics, Faculty of Sciences of Bizerte, 7021 Zarzouna (Tunisia); Ezzaouia, Hatem [Photovoltaic Laboratory Research and Technology Centre of Energy, Borj-Cedria Science and Technology Park, BP 95, 2050 Hammam-Lif (Tunisia)

    2012-04-01

    Photoluminescence and optical properties of porous oxide films formed by two-step aluminum anodization at a fixed current 200 mA have been investigated. It was found that the crystallographic structure depend strongly on the annealing temperature. X-ray diffraction (XRD) reveals an amorphisation of the porous oxide films after annealing. This evolution has been confirmed by Raman spectroscopy measurement. Spectroscopic ellipsometry (SE) in the UV-vis and near infra red (IR) spectra shows that refraction index n increases and the extinction coefficient k decreases with annealing temperature. This observation has been confirmed with reflectivity measurements. As a consequence the reflectivity reaches 97% when porous alumina films were annealed at 650 Degree-Sign C. Photoluminescence (PL) measurements show two PL peaks in the emission and excitation spectra. The first emission peak is centered at 460 nm ({alpha}-band) and the second ({beta}-band) shifts from 500 to 525 nm, depending on excitation wavelength. For excitation spectra, one spectral peak is located at 271 nm and the second shifts to longer wavelengths with increasing emission wavelength. The results indicate the existence of two PL centers. One is associated with oxygen adsorption at the pore wall and oxygen vacancies inside the alumina. The other is related to the adsorption of water and/or OH groups at the surface of the pore wall and to structure defects and sulfur inclusion inside the films.

  1. Sulfur Poisoning of the Water Gas Shift Reaction on Anode Supported Solid Oxide Fuel Cells

    DEFF Research Database (Denmark)

    Hagen, Anke

    2013-01-01

    Investigation of fuels containing sulfur impurities is important regarding durability of solid oxide fuel cells (SOFC) because they are present in various potential fuels for SOFC applications. The effect of H2S in the ppm range on the performance of state-of-the-art anode supported SOFC at 850...... and 750°C is evaluated in either hydrogen/steam or hydrogen/steam/CO fuel. It was found that the poisoning effect is more severe in H2/H2O/CO vs. H2/H2O fuel. Only ∼8 ppm H2S can be allowed in the CO containing fuel without risking damage to the anode, whereas 90 ppm (or even more) is possible in H2/H2O...

  2. Methane Steam Reforming over an Ni-YSZ Solid Oxide Fuel Cell Anode in Stack Configuration

    Directory of Open Access Journals (Sweden)

    D. Mogensen

    2014-01-01

    Full Text Available The kinetics of catalytic steam reforming of methane over an Ni-YSZ anode of a solid oxide fuel cell (SOFC have been investigated with the cell placed in a stack configuration. In order to decrease the degree of conversion, a single cell stack with reduced area was used. Measurements were performed in the temperature range 600–800°C and the partial pressures of all reactants and products were varied. The obtained rates could be well fitted with a power law expression (r ∝PCH40.7. A simple model is presented which is capable of predicting the methane conversion in a stack configuration from intrinsic kinetics of the anode support material. The predictions are compared with the stack measurements presented here, and good agreement is observed.

  3. Characterization of Anodic Aluminum Oxide Membrane with Variation of Crystallizing Temperature for pH Sensor.

    Science.gov (United States)

    Yeo, Jin-Ho; Lee, Sung-Gap; Jo, Ye-Won; Jung, Hye-Rin

    2015-11-01

    We fabricated electrolyte-dielectric-metal (EDM) device incorporating a high-k Al2O3 sensing membrane from a porous anodic aluminum oxide (AAO) using a two step anodizing process for pH sensors. In order to change the properties of the AAO template, the crystallizing temperature was varied from 400 degrees C to 700 degrees C over 2 hours. The structural properties were observed by field emission scanning electron microscopy (FE-SEM). The pH sensitivity increased with an increase in the crystallizing temperature from 400 degrees C to 600 degrees C. However at 700 degrees C, deformation occurred. The porous AAO sensor with a crystallizing temperature of 600 degrees C displayed the good sensitivity and long-term stability and the values were 55.7 mV/pH and 0.16 mV/h, respectively. PMID:26726567

  4. Effects of laminating and co-firing conditions on the performance of anode-supported Ce0.8Sm0.201.9 film electrolyte

    Directory of Open Access Journals (Sweden)

    Li X.

    2011-01-01

    Full Text Available In order to evaluate the laminating and co-firing technique on the performance of anode-supported Ce0.8Sm0.2O1.9 (SDC film electrolyte and its single cell, NiO-YSZ and NiOSDC anode-supported SDC film electrolytes were fabricated by laminating 24 sheets of anode plus one sheet of electrolyte and co-firing. La0.4Sr0.6Co0.2Fe0.8O3-δ (LSCF-SDC cathode was coated on the SDC electrolytes to form a single cell. The lamination was tried at different laminating temperatures and pressures and the co-firing was carried out at different temperatures. The results showed that the laminating temperature should above the glass transition temperature (Tg of the binder. The laminating pressure of 70 MPa resulted in warp of the samples. The best co-firing temperature of the anode-supported SDC film electrolyte was 1400°C. The SDC film electrolyte formed well adherence to the anode. The NiO-YSZ anode had larger flexural strength than the NiO-SDC anode. The NiO-YSZ anode-supported SDC film electrolyte single cell had an open circuit voltage of 0.803 V and a maximum power density of 93.03 mW/cm2 with hydrogen as fuel at 800°C.

  5. Sputtered tin oxide and titanium oxide thin films as alternative transparent conductive oxides

    Energy Technology Data Exchange (ETDEWEB)

    Boltz, Janika

    2011-12-12

    Alternative transparent conductive oxides to tin doped indium oxide have been investigated. In this work, antimony doped tin oxide and niobium doped titanium oxide have been studied with the aim to prepare transparent and conductive films. Antimony doped tin oxide and niobium doped titanium oxide belong to different groups of oxides; tin oxide is a soft oxide, while titanium oxide is a hard oxide. Both oxides are isolating materials, in case the stoichiometry is SnO{sub 2} and TiO{sub 2}. In order to achieve transparent and conductive films free carriers have to be generated by oxygen vacancies, by metal ions at interstitial positions in the crystal lattice or by cation doping with Sb or Nb, respectively. Antimony doped tin oxide and niobium doped titanium oxide films have been prepared by reactive direct current magnetron sputtering (dc MS) from metallic targets. The process parameters and the doping concentration in the films have been varied. The films have been electrically, optically and structurally analysed in order to analyse the influence of the process parameters and the doping concentration on the film properties. Post-deposition treatments of the films have been performed in order to improve the film properties. For the deposition of transparent and conductive tin oxide, the dominant parameter during the deposition is the oxygen content in the sputtering gas. The Sb incorporation as doping atoms has a minor influence on the electrical, optical and structural properties. Within a narrow oxygen content in the sputtering gas highly transparent and conductive tin oxide films have been prepared. In this study, the lowest resistivity in the as deposited state is 2.9 m{omega} cm for undoped tin oxide without any postdeposition treatment. The minimum resistivity is related to a transition to crystalline films with the stoichiometry of SnO{sub 2}. At higher oxygen content the films turn out to have a higher resistivity due to an oxygen excess. After post

  6. Hollow carbon nanospheres/silicon/alumina core-shell film as an anode for lithium-ion batteries

    OpenAIRE

    Li, Bing; Yao, Fei; Bae, Jung Jun; Chang, Jian; Zamfir, Mihai Robert; Le, Duc Toan; Pham, Duy Tho; Yue, Hongyan; Lee, Young Hee

    2015-01-01

    Hollow carbon nanospheres/silicon/alumina (CNS/Si/Al2O3) core-shell films obtained by the deposition of Si and Al2O3 on hollow CNS interconnected films are used as the anode materials for lithium-ion batteries. The hollow CNS film acts as a three dimensional conductive substrate and provides void space for silicon volume expansion during electrochemical cycling. The Al2O3 thin layer is beneficial to the reduction of solid-electrolyte interphase (SEI) formation. Moreover, as-designed structure...

  7. Damp heat stable doped zinc oxide films

    Energy Technology Data Exchange (ETDEWEB)

    Hüpkes, J., E-mail: j.huepkes@fz-juelich.de [IEK5–Photovoltaik, Forschungszentrum Jülich GmbH, 52425 Jülich (Germany); Owen, J.I. [IEK5–Photovoltaik, Forschungszentrum Jülich GmbH, 52425 Jülich (Germany); Wimmer, M.; Ruske, F. [Institute of Silicon Photovoltaics, Helmholtz-Zentrum Berlin für Materialien und Energie, Kekuléstraße 5, 12489 Berlin (Germany); Greiner, D.; Klenk, R. [Institute for Heterogeneous Materials Systems, Helmholtz-Zentrum Berlin für Materialien und Energie, Hahn-Meitner-Platz 1, 14109 Berlin (Germany); Zastrow, U. [IEK5–Photovoltaik, Forschungszentrum Jülich GmbH, 52425 Jülich (Germany); Hotovy, J. [IEK5–Photovoltaik, Forschungszentrum Jülich GmbH, 52425 Jülich (Germany); Faculty of Electrical Engineering and Information Technology, Slovak University of Technology, Ilkovicova 3, 812 19 Bratislava (Slovakia)

    2014-03-31

    Zinc oxide is widely used as transparent contact in thin film solar cells. We investigate the damp heat stability of aluminum doped ZnO (ZnO:Al) films sputter deposited at different conditions. Increase in resistivity upon damp heat exposure was observed for as-deposited ZnO:Al films and the water penetration was directly linked to this degradation. Deuterium was used as isotopic marker to identify the amount of water taken up by the films. Finally, we applied a special annealing step to prepare highly stable ZnO:Al films with charge carrier mobility of 70 cm{sup 2}/Vs after 1000 h of damp heat treatment. A grain boundary reconstruction model is proposed to explain the high stability of ZnO:Al films after annealing. - Highlights: • Study of damp heat degradation on electrical properties of ZnO:Al • Demonstration of fast water penetration and replacement mechanism • Damp heat stable ZnO:Al films with high mobility after damp heat treatment.

  8. Characterization and quantification of oxides generated by anodization on titanium for implantation purposes

    Science.gov (United States)

    Aloia Games, L.; Pastore, J.; Bouchet, A.; Ballarre, J.

    2011-12-01

    The use of titanium as implant material is widely known in the surgery field. The formation of natural or artificial compact and protective oxide is a convenient tool for metal protection and a good way to generate phosphate deposits to enhance biocompatibility and bone fixation with the existing tissue. The present work has the aim of superficially modify commercially pure titanium sheets used in orthopedics and odontology, with a potencistatic anodization process with an ammonium phosphate and ammonium fluoride solution as electrolyte. The objective is to generate titanium oxides doped with phosphorous on the surface, to promote bioactivity. The characterization and quantification of the generated deposits is presented as a starting point for the future application of these materials. The applied characterization methods are X ray diffraction, micro-Raman spectroscopy analysis for evaluating the chemical and phase composition on the modified surface and PDI image analysis techniques that allow the segmentation of SEM images and the measurement and quantification of the oxides generated by the anodization process. The samples with polished treated surface at 30V have the deposit of a phosphate rich thick layer covering almost all the surface and spherical-shaped titanium oxide crystals randomly placed (covering more than 20% of the surface area).

  9. Characterization and quantification of oxides generated by anodization on titanium for implantation purposes

    International Nuclear Information System (INIS)

    The use of titanium as implant material is widely known in the surgery field. The formation of natural or artificial compact and protective oxide is a convenient tool for metal protection and a good way to generate phosphate deposits to enhance biocompatibility and bone fixation with the existing tissue. The present work has the aim of superficially modify commercially pure titanium sheets used in orthopedics and odontology, with a potencistatic anodization process with an ammonium phosphate and ammonium fluoride solution as electrolyte. The objective is to generate titanium oxides doped with phosphorous on the surface, to promote bioactivity. The characterization and quantification of the generated deposits is presented as a starting point for the future application of these materials. The applied characterization methods are X ray diffraction, micro-Raman spectroscopy analysis for evaluating the chemical and phase composition on the modified surface and PDI image analysis techniques that allow the segmentation of SEM images and the measurement and quantification of the oxides generated by the anodization process. The samples with polished treated surface at 30V have the deposit of a phosphate rich thick layer covering almost all the surface and spherical-shaped titanium oxide crystals randomly placed (covering more than 20% of the surface area).

  10. Anodic oxidation of salicylic acid on BDD electrode: Variable effects and mechanisms of degradation

    International Nuclear Information System (INIS)

    Highlights: ► Oxidation with BDD is a powerful electrochemical method able to mineralize. ► SA is oxidized to aromatic compounds then CO2 and H2O. ► Polymeric intermediate products were formed. - Abstract: The degradation of 100 mL of solution with salicylic acid (SA) in the pH range 3.0–10.0 has been studied by anodic oxidation in a cell with a boron-doped diamond (BDD) anode and a stainless steel cathode, both of 3 cm2 area, by applying a current of 100, 300 and 450 mA at 25 °C. Completed mineralization is always achieved due to the great concentration of hydroxyl radical (·OH) generated at the BDD surface. The mineralization rate increases with increasing applied current, but decreases when drug concentration rises from 200 mg L−1. Nevertheless, the pH effect was not significant. During oxidation it was observed that catechol, 2,5-dihydroxylated benzoic acid, 2,3-dihydroxylated benzoic acid and hydroquinone were formed as aromatic intermediates. In addition, ion-exclusion chromatography allowed the detection of fumaric, maleic, oxalic and formic as the ultimate carboxylic acid.

  11. Novel Size and Surface Oxide Effects in Silicon Nanowires as Lithium Battery Anodes

    KAUST Repository

    McDowell, Matthew T.

    2011-09-14

    With its high specific capacity, silicon is a promising anode material for high-energy lithium-ion batteries, but volume expansion and fracture during lithium reaction have prevented implementation. Si nanostructures have shown resistance to fracture during cycling, but the critical effects of nanostructure size and native surface oxide on volume expansion and cycling performance are not understood. Here, we use an ex situ transmission electron microscopy technique to observe the same Si nanowires before and after lithiation and have discovered the impacts of size and surface oxide on volume expansion. For nanowires with native SiO2, the surface oxide can suppress the volume expansion during lithiation for nanowires with diameters <∼50 nm. Finite element modeling shows that the oxide layer can induce compressive hydrostatic stress that could act to limit the extent of lithiation. The understanding developed herein of how volume expansion and extent of lithiation can depend on nanomaterial structure is important for the improvement of Si-based anodes. © 2011 American Chemical Society.

  12. Anodic oxidation of salicylic acid on BDD electrode: Variable effects and mechanisms of degradation

    Energy Technology Data Exchange (ETDEWEB)

    Rabaaoui, Nejmeddine, E-mail: chimie_tunisie@yahoo.fr [Faculte des Sciences de Sfax, Departement de Chimie, 3038 Sfax (Tunisia); Allagui, Mohamed Salah [Faculte des Sciences de Gafsa, Campus Universitaire Sidi Ahmed Zarrouk, 2112 Gafsa (Tunisia)

    2012-12-15

    Highlights: Black-Right-Pointing-Pointer Oxidation with BDD is a powerful electrochemical method able to mineralize. Black-Right-Pointing-Pointer SA is oxidized to aromatic compounds then CO{sub 2} and H{sub 2}O. Black-Right-Pointing-Pointer Polymeric intermediate products were formed. - Abstract: The degradation of 100 mL of solution with salicylic acid (SA) in the pH range 3.0-10.0 has been studied by anodic oxidation in a cell with a boron-doped diamond (BDD) anode and a stainless steel cathode, both of 3 cm{sup 2} area, by applying a current of 100, 300 and 450 mA at 25 Degree-Sign C. Completed mineralization is always achieved due to the great concentration of hydroxyl radical ({center_dot}OH) generated at the BDD surface. The mineralization rate increases with increasing applied current, but decreases when drug concentration rises from 200 mg L{sup -1}. Nevertheless, the pH effect was not significant. During oxidation it was observed that catechol, 2,5-dihydroxylated benzoic acid, 2,3-dihydroxylated benzoic acid and hydroquinone were formed as aromatic intermediates. In addition, ion-exclusion chromatography allowed the detection of fumaric, maleic, oxalic and formic as the ultimate carboxylic acid.

  13. PEALD YSZ-based bilayer electrolyte for thin film-solid oxide fuel cells

    Science.gov (United States)

    Yu, Wonjong; Cho, Gu Young; Hong, Soonwook; Lee, Yeageun; Kim, Young Beom; An, Jihwan; Cha, Suk Won

    2016-10-01

    Yttria-stabilized zirconia (YSZ) thin film electrolyte deposited by plasma enhanced atomic layer deposition (PEALD) was investigated. PEALD YSZ-based bi-layered thin film electrolyte was employed for thin film solid oxide fuel cells on nanoporous anodic aluminum oxide substrates, whose electrochemical performance was compared to the cell with sputtered YSZ-based electrolyte. The cell with PEALD YSZ electrolyte showed higher open circuit voltage (OCV) of 1.0 V and peak power density of 182 mW cm-2 at 450 °C compared to the one with sputtered YSZ electrolyte(0.88 V(OCV), 70 mW cm-2(peak power density)). High OCV and high power density of the cell with PEALD YSZ-based electrolyte is due to the reduction in ohmic and activation losses as well as the gas and electrical current tightness.

  14. Electrical analysis of niobium oxide thin films

    Energy Technology Data Exchange (ETDEWEB)

    Graça, M.P.F., E-mail: mpfg@ua.pt [I3N & Physics Department, Aveiro University, Campus Universitário de Santiago, 3810-193 Aveiro (Portugal); Saraiva, M. [I3N & Physics Department, Aveiro University, Campus Universitário de Santiago, 3810-193 Aveiro (Portugal); Freire, F.N.A. [Mechanics Engineering Department, Ceará Federal University, Fortaleza (Brazil); Valente, M.A.; Costa, L.C. [I3N & Physics Department, Aveiro University, Campus Universitário de Santiago, 3810-193 Aveiro (Portugal)

    2015-06-30

    In this work, a series of niobium oxide thin films was deposited by reactive magnetron sputtering. The total pressure of Ar/O{sub 2} was kept constant at 1 Pa, while the O{sub 2} partial pressure was varied up to 0.2 Pa. The depositions were performed in a grounded and non-intentionally heated substrate, resulting in as-deposited amorphous thin films. Raman spectroscopy confirmed the absence of crystallinity. Dielectric measurements as a function of frequency (40 Hz–110 MHz) and temperature (100 K–360 K) were performed. The dielectric constant for the film samples with thickness (d) lower than 650 nm decreases with the decrease of d. The same behaviour was observed for the conductivity. These results show a dependence of the dielectric permittivity with the thin film thickness. The electrical behaviour was also related with the oxygen partial pressure, whose increment promotes an increase of the Nb{sub 2}O{sub 5} stoichiometry units. - Highlights: • Niobium oxide thin films were deposited by reactive magnetron sputtering. • XRD showed a phase change with the increase of the P(O{sub 2}). • Raman showed that increasing P(O{sub 2}), Nb{sub 2}O{sub 5} amorphous increases. • Conductivity tends to decrease with the increase of P(O{sub 2}). • Dielectric analysis indicates the inexistence of preferential grow direction.

  15. Electrical analysis of niobium oxide thin films

    International Nuclear Information System (INIS)

    In this work, a series of niobium oxide thin films was deposited by reactive magnetron sputtering. The total pressure of Ar/O2 was kept constant at 1 Pa, while the O2 partial pressure was varied up to 0.2 Pa. The depositions were performed in a grounded and non-intentionally heated substrate, resulting in as-deposited amorphous thin films. Raman spectroscopy confirmed the absence of crystallinity. Dielectric measurements as a function of frequency (40 Hz–110 MHz) and temperature (100 K–360 K) were performed. The dielectric constant for the film samples with thickness (d) lower than 650 nm decreases with the decrease of d. The same behaviour was observed for the conductivity. These results show a dependence of the dielectric permittivity with the thin film thickness. The electrical behaviour was also related with the oxygen partial pressure, whose increment promotes an increase of the Nb2O5 stoichiometry units. - Highlights: • Niobium oxide thin films were deposited by reactive magnetron sputtering. • XRD showed a phase change with the increase of the P(O2). • Raman showed that increasing P(O2), Nb2O5 amorphous increases. • Conductivity tends to decrease with the increase of P(O2). • Dielectric analysis indicates the inexistence of preferential grow direction

  16. Electrochromic performance, wettability and optical study of copper manganese oxide thin films: Effect of annealing temperature

    International Nuclear Information System (INIS)

    In the present work, the nanostructured copper manganese oxide (CMO) thin films were prepared from acetate based sol–gel precursors and deposited on glass and indium tin oxide (ITO) substrates by dip-coating technique. The films were annealed at 300, 400 and 500 °C in ambient atmosphere. The effects of annealing temperature on structural, morphological, wettability, electrochromic and optical properties of CMO thin films were characterized by X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), energy dispersive spectroscopy (EDX), water contact angle measurement (WCA), cyclic voltammetry (CV) measurements and ultraviolet–visible (UV–vis) spectrophotometery. The presence of mixed oxide phases comprising of copper manganese oxide (CuMn2O4) and manganese oxide at different annealing temperature was confirmed by XRD patterns. The results showed that the Mn3O4 phase has been changed to Mn2O3 when the annealing temperature is increased from 300 to 500 °C. The FESEM images indicated that the granular surface morphology was sensitive to annealing temperature. EDX studies indicated that the thin films contained O, Mn and Cu species. Wettability studies showed that the water contact angle of the nanostructured CMO thin films coated on glass substrates was influenced by the variation of annealing temperature and the surface nature of thin films was changed from hydrophilic to hydrophobic. The results of CVs measurement indicated that the anodic and cathodic charge density and capacitance of all CMO samples decreased with increasing scan rate in potential range of −1–1 eV. Also, the annealed CMO thin film at 500 °C showed better electrochromic performance with respect to other samples at lower scan rate. The thickness, refractive index, extinction coefficient and optical band gap of thin films coated on glass substrates were calculated from reflectance and transmittance spectra using an iterative numerical method. The optical band gap of

  17. Production of planar copper-based anode supported intermediate temperature solid oxide fuel cells cosintered at 950 °C

    Science.gov (United States)

    De Marco, Vincenzo; Grazioli, Alberto; Sglavo, Vincenzo M.

    2016-10-01

    Copper-based anode supported planar Intermediate Temperature Solid Oxide Fuel Cells are produced and characterized in the present work. The most important advancement is related to the use of copper within the anodic layer, this giving promising results for feeding Intermediate Temperature Solid Oxide Fuel Cells with carbon and sulphur containing fuels. Both anode and Li2O containing-Gadolinia Doped Ceria based electrolyte are produced by water based tape casting process. The supporting anode is coupled to the electrolyte by thermopressing, the cathode being obtained by screen printing. A 3 h isotherm at 950 °C allows to obtain the cosintering of the three layers. The electrochemical test performed on such cells reveals a 0.8 V open circuit voltage and a power density higher than 26 mW cm-2 at 650 °C.

  18. Interfacial Assembly of Graphene Oxide Films

    Science.gov (United States)

    Valtierrez, Cain; Ismail, Issam; Macosko, Christopher; Stottrup, Benjamin

    Controlled assembly of monolayer graphene-oxide (GO) films at the air/water interface is of interest for the development of transparent conductive thin films of chemically-derived graphene. We present experimental results from investigations of the assembly of polydisperse GO sheets at the air-water interface. GO nanosheets with lateral dimensions of greater than 10 microns were created using a modified Tour synthesis (Dimiev and Tour, 2014). GO films were generated with conventional Langmuir trough techniques to control lateral packing density. Film morphology was characterized in situ with Brewster angle microscopy. Films were transferred unto a substrate via the Langmuir-Blodgett deposition technique and imaged with fluorescence quenching microscopy. Through pH modulation of the aqueous subphase, it was found that GO's intrinsic surface activity to the interface increased with increasing subphase acidity. Finally, we found a dominant elastic contribution during uniaxial film deformation as measured by anisotropic pressure measurements. A. M. Dimiev, and J. M. Tour, ``Mechanism of GO Formation,'' ACS Nano, 8, (2014)

  19. Influence of electropolishing and anodic oxidation on morphology, chemical composition and corrosion resistance of niobium

    International Nuclear Information System (INIS)

    The work presents results of the studies performed on electropolishing of pure niobium in a bath that contained: sulphuric acid, hydrofluoric acid, ethylene glycol and acetanilide. After the electropolishing, the specimens were subjected to anodic passivation in a 1 mol dm−3 phosphoric acid solution at various voltages. The surface morphology, thickness, roughness and chemical composition of the resulting oxide layers were analysed. Thusly prepared niobium samples were additionally investigated in terms of their corrosion resistance in Ringer's solution. The electropolished niobium surface was determined to be smooth and lustrous. The anodisation led to the growth of barrier-like oxide layers, which were enriched in phosphorus species. - Highlights: • Pure niobium was electropolished and subsequently anodised in a H3PO4 solution. • Phosphorus was successfully introduced into the oxide layers after the treatment. • Corrosion resistance of niobium in Ringer's solution was improved after anodising

  20. Morphology of Platinum Nanowire Array Electrodeposited Within Anodic Aluminium Oxide Template Characterized by Atomic Force Microscopy

    Institute of Scientific and Technical Information of China (English)

    孔令斌; 陆梅; 李梦轲; 郭新勇; 力虎林

    2003-01-01

    Uniform platinum nanowires were synthesized by electrodepositing the platinum under a very low altering current frequency (20Hz) and increasing voltage (5-15 V) in the pores of anodic aluminium oxide (AAO) template.Atomic force microscopy observation indicates that the template membranes we obtained have hexagonally closepacked nanochannels. The platinum nanowires have highly ordered arrays after partially dissolving the aluminium oxide membrane. With the increasing dissolving time, the platinum nanowire array collapsed. A concave topography of the aluminium substrate was observed after the aluminium oxide membrane was dissolved completely and the platinum nanowires were released from the template. Platinum nanowires were also characterized by transmission electron microscopy and the phase structure of the Al/AAO/Pt composite was proven by x-ray diffraction.

  1. Production of nickel oxide thin films by magnetron sputtering

    International Nuclear Information System (INIS)

    Discrepancies between short-circuit diffusion data derived from nickel oxide bicrystals and specimens produced by the oxidation of nickel has led to a requirement for thin film nickel oxide specimens of controlled microstructure and impurity level that can be produced independently of the oxidation process. RF magnetron sputtering of nickel oxide has been used to produce thin films intended for this application. The as-deposited films contain excess oxygen compared to stoichiometric nickel oxide and exhibit strong preferred orientation. Annealing in argon leads to oxygen deficient films. The reduction in porosity which accompanies the annealing leads to the formation of through-thickness cracks in the films. Subsequent oxygen tracer studies demonstrate that the cracks give rise to excessive oxygen transport through the films compared to that expected for thermally oxidised scales. The microstructural anomalies produced by the annealing process mean that the required microstructures were not achieved and these films are not useful analogues of thermal nickel oxide scales. (author)

  2. Direct Growth of Bismuth Film as Anode for Aqueous Rechargeable Batteries in LiOH, NaOH and KOH Electrolytes

    Directory of Open Access Journals (Sweden)

    Wenhua Zuo

    2015-10-01

    Full Text Available As promising candidates for next-generation energy storage devices, aqueous rechargeable batteries are safer and cheaper than organic Li ion batteries. But due to the narrow voltage window of aqueous electrolytes, proper anode materials with low redox potential and high capacity are quite rare. In this work, bismuth electrode film was directly grown by a facile hydrothermal route and tested in LiOH, NaOH and KOH electrolytes. With low redox potential (reduction/oxidation potentials at ca. −0.85/−0.52 V vs. SCE, respectively and high specific capacity (170 mAh·g−1 at current density of 0.5 A·g−1 in KOH electrolyte, Bi was demonstrated as a suitable anode material for aqueous batteries. Furthermore, by electrochemical impedance spectroscopy (EIS analysis, we found that with smaller Rs and faster ion diffusion coefficient, Bi electrode film in KOH electrolyte exhibited better electrochemical performance than in LiOH and NaOH electrolytes.

  3. Marker behaviour of implanted xenon during the anodic oxidation of aluminium: evidence and interpretation of dose dependant splitting effect

    International Nuclear Information System (INIS)

    Using 2 MeV lithium ions backscattering and transmission electron microscopy techniques, a part of xenon atoms introduced by implantation in aluminium metal under the initial oxide layer is shown to be tranported by the moving metal-oxide interface during anodic oxidation. From specific anodization conditions (V sup(ct), T = 900C) this splitting of the initial xenon distribution is interpreted in terms of bubble formation and growth above a given local concentration threshold. A schematic model for this behaviour evolution is proposed. This dose dependance is of practical interest in the determination of transport numbers. Although unambiguously measured they may be subject to significant systematic uncertainties which are discussed

  4. Reduced Graphene Oxide Thin Film on Conductive Substrates by Bipolar Electrochemistry

    Science.gov (United States)

    Anis, Allagui; Mohammad, Ali Abdelkareem; Hussain, Alawadhi; Ahmed, S. Elwakil

    2016-01-01

    Recent years have shown an increased interest in developing manufacturing processes for graphene and its derivatives that consider the environmental impact and large scale cost-effectiveness. However, today’s most commonly used synthesis routes still suffer from their excessive use of harsh chemicals and/or the complexity and financial cost of the process. Furthermore, the subsequent transfer of the material onto a substrate makes the overall process even more intricate and time-consuming. Here we describe a single-step, single-cell preparation procedure of metal-supported reduced graphene oxide (rGO) using the principle of bipolar electrochemistry of graphite in deionized water. Under the effect of an electric field between two stainless steel feeder electrodes, grapheme layers at the anodic pole of the wireless graphite were oxidized into colloidal dispersion of GO, which migrated electrophoretically towards the anodic side of the cell, and deposited in the form of rGO (d(002) = 0.395 nm) by van der Waals forces. For substrates chemically more susceptible to the high anodic voltage, we show that the electrochemical setup can be adapted by placing the latter between the wireless graphite and the stainless steel feeder anode. This method is straightforward, inexpensive, environmentally-friendly, and could be easily scaled up for high yield and large area production of rGO thin films. PMID:26883173

  5. Reduced Graphene Oxide Thin Film on Conductive Substrates by Bipolar Electrochemistry

    Science.gov (United States)

    Anis, Allagui; Mohammad, Ali Abdelkareem; Hussain, Alawadhi; Ahmed, S. Elwakil

    2016-02-01

    Recent years have shown an increased interest in developing manufacturing processes for graphene and its derivatives that consider the environmental impact and large scale cost-effectiveness. However, today’s most commonly used synthesis routes still suffer from their excessive use of harsh chemicals and/or the complexity and financial cost of the process. Furthermore, the subsequent transfer of the material onto a substrate makes the overall process even more intricate and time-consuming. Here we describe a single-step, single-cell preparation procedure of metal-supported reduced graphene oxide (rGO) using the principle of bipolar electrochemistry of graphite in deionized water. Under the effect of an electric field between two stainless steel feeder electrodes, grapheme layers at the anodic pole of the wireless graphite were oxidized into colloidal dispersion of GO, which migrated electrophoretically towards the anodic side of the cell, and deposited in the form of rGO (d(002) = 0.395 nm) by van der Waals forces. For substrates chemically more susceptible to the high anodic voltage, we show that the electrochemical setup can be adapted by placing the latter between the wireless graphite and the stainless steel feeder anode. This method is straightforward, inexpensive, environmentally-friendly, and could be easily scaled up for high yield and large area production of rGO thin films.

  6. Cycle Life of Commercial Lithium-Ion Batteries with Lithium Titanium Oxide Anodes in Electric Vehicles

    Directory of Open Access Journals (Sweden)

    Xuebing Han

    2014-07-01

    Full Text Available The lithium titanium oxide (LTO anode is widely accepted as one of the best anodes for the future lithium ion batteries in electric vehicles (EVs, especially since its cycle life is very long. In this paper, three different commercial LTO cells from different manufacturers were studied in accelerated cycle life tests and their capacity fades were compared. The result indicates that under 55 °C, the LTO battery still shows a high capacity fade rate. The battery aging processes of all the commercial LTO cells clearly include two stages. Using the incremental capacity (IC analysis, it could be judged that in the first stage, the battery capacity decreases mainly due to the loss of anode material and the degradation rate is lower. In the second stage, the battery capacity decreases much faster, mainly due to the degradation of the cathode material. The result is important for the state of health (SOH estimation and remaining useful life (RUL prediction of battery management system (BMS for LTO batteries in EVs.

  7. Accelerated creep in solid oxide fuel cell anode supports during reduction

    Science.gov (United States)

    Frandsen, H. L.; Makowska, M.; Greco, F.; Chatzichristodoulou, C.; Ni, D. W.; Curran, D. J.; Strobl, M.; Kuhn, L. T.; Hendriksen, P. V.

    2016-08-01

    To evaluate the reliability of solid oxide fuel cell (SOFC) stacks during operation, the stress field in the stack must be known. During operation the stress field will depend on time as creep processes relax stresses. The creep of reduced Ni-YSZ anode support at operating conditions has been studied previously. In this work a newly discovered creep phenomenon taking place during the reduction is reported. This relaxes stresses at a much higher rate (∼×104) than creep during operation. The phenomenon was studied both in three-point bending and uniaxial tension. Differences between the two measurements could be explained by newly observed stress promoted reduction. Finally, samples exposed to a small tensile stress (∼0.004 MPa) were observed to expand during reduction, which is in contradiction to previous literature. These observations suggest that release of internal residual stresses between the NiO and the YSZ phases occurs during reduction. The accelerated creep should practically eliminate any residual stress in the anode support in an SOFC stack, as has previously been indirectly observed. This phenomenon has to be taken into account both in the production of stacks and in the simulation of the stress field in a stack based on anode supported SOFCs.

  8. Vanadium Sulfide on Reduced Graphene Oxide Layer as a Promising Anode for Sodium Ion Battery.

    Science.gov (United States)

    Sun, Ruimin; Wei, Qiulong; Li, Qidong; Luo, Wen; An, Qinyou; Sheng, Jinzhi; Wang, Di; Chen, Wei; Mai, Liqiang

    2015-09-23

    As an alternative system of rechargeable lithium ion batteries, sodium ion batteries revitalize researchers' interest due to the low cost, abundant sodium resources, and similar storage mechanism to lithium ion batteries. VS4 has emerged as a promising anode material for SIBs due to low cost and its unique linear chains structure that can offer potential sites for sodium storage. Herein, we present the growth of VS4 on reduced graphene oxide (rGO) as SIBs anode for the first time. The VS4/rGO anode exhibits promising performance in SIBs. It delivers a reversible capacity of 362 mAh g(-1) at 100 mA g(-1) and a good rate performance. We also investigate the sodium storage behavior of the VS4/rGO. Different than most transition metal sulfides, the VS4/rGO composite experiences a three-step separation mechanism during the sodiation process (VS4 to metallic V and Na2S, then the electrochemical mechanism is akin to Na-S). The VS4/rGO composite proves to be a promising material for rechargeable SIBs.

  9. Fabrication of High power, High-Efficiency Linear Array Diode Lasers by Pulse Anodic Oxidation

    Science.gov (United States)

    Gao, Xin; Zhang, Jing; Li, Hui; Qu, Yi; Bo, Baoxue

    2006-09-01

    InGaAlAs/AlGaAs/GaAs double-quantum-well (DQW) linear array diode lasers with asymmetric wide waveguide have been successfully fabricated by pulse anodic oxidation upon molecular beam epitaxy material growth. High-efficiency and high-power quasi-continuous-wave (QCW) output has been realized at 808 nm wavelength. The threshold current and slope efficiency of the prepared high-fill-factor QCW devices are 24 A and 1.25 A/W, respectively, and a maximum wall-plug efficiency of 51% has been achieved.

  10. Preparation and Characterization of Fe Nanowire Arrays Embedded in Porous Anodic Aluminum Oxide Templates

    Institute of Scientific and Technical Information of China (English)

    迟广俊; 姚素薇

    2004-01-01

    Fe nanowire arrays are prepared by electrodeposition in porous anodic aluminum oxide template from a composite electrolyte solution. These nanowires have an uniform diameter of approximate 25 nm and a length in excess of 2.5μm.The micrographs and crystal structures of Fe nanowlres are studied by transmission electron microscopy (TEM), selected-area electron diffraction (SAED), and X-ray diffraction(XRD). It is found that each nanowire is essentially a single crystal and has a different orientation in each array. Hysteresis loops of Fe nanowire array show that its easy magnetization direction is perpendicular to the sample plane.

  11. Methane Steam Reforming over an Ni-YSZ Solid Oxide Fuel Cell Anode in Stack Configuration

    DEFF Research Database (Denmark)

    Mogensen, David; Grunwaldt, Jan-Dierk; Hendriksen, Peter Vang;

    2014-01-01

    The kinetics of catalytic steam reforming of methane over an Ni-YSZ anode of a solid oxide fuel cell (SOFC) have been investigated with the cell placed in a stack configuration. In order to decrease the degree of conversion, a single cell stack with reduced area was used. Measurements were...... performed in the temperature range 600-800 degrees C and the partial pressures of all reactants and products were varied. The obtained rates could be well fitted with a power law expression (r proportional to P-CH4(0.7)). A simple model is presented which is capable of predicting the methane conversion...

  12. Methane Steam Reforming over an Ni-YSZ Solid Oxide Fuel Cell Anode in Stack Configuration

    OpenAIRE

    Mogensen, D.; J.-D. Grunwaldt; Hendriksen, P. V.; J. U. Nielsen; K. Dam-Johansen

    2014-01-01

    The kinetics of catalytic steam reforming of methane over an Ni-YSZ anode of a solid oxide fuel cell (SOFC) have been investigated with the cell placed in a stack configuration. In order to decrease the degree of conversion, a single cell stack with reduced area was used. Measurements were performed in the temperature range 600-800 degrees C and the partial pressures of all reactants and products were varied. The obtained rates could be well fitted with a power law expression (r proportional ...

  13. Accelerated creep in solid oxide fuel cell anode supports during reduction

    DEFF Research Database (Denmark)

    Frandsen, Henrik Lund; Makowska, Malgorzata Grazyna; Greco, Fabio;

    2016-01-01

    To evaluate the reliability of solid oxide fuel cell (SOFC) stacks during operation, the stress field in the stack must be known. During operation the stress field will depend on time as creep processes relax stresses. The creep of reduced Ni-YSZ anode support at operating conditions has been...... studied previously. In this work a newly discovered creep phenomenon taking place during the reduction is reported. This relaxes stresses at a much higher rate (∼ x104) than creep during operation. The phenomenon was studied both in three-point bending and uniaxial tension. Differences between the two...

  14. The beneficial effect of nanocrystalline and amorphous nature on the anode performance of manganese oxide for lithium ion batteries

    International Nuclear Information System (INIS)

    Highlights: • A soft-chemical redox reaction yields efficient anode material of amorphous MnO2 nanocrystal. • Amorphous MnO2 nanocrystal shows better anode performance than well-crystalline homologue. • This result highlights the merit of nanocrystalline nature for the electrode performance of MnO2. • The present redox reaction provides a scalable and economic route to efficient anode material. - Abstract: The effect of the amorphous structure and nanocrystalline nature of metal oxide on its anode performance in lithium ion batteries is investigated with two nanocrystalline and one well-crystallized layered manganese oxides. X-ray amorphous manganese oxide nanocrystals are synthesized by soft-chemical redox reactions using reducing agents of KBH4 and LiI at room temperature, whereas well-crystallized layered manganese oxide is obtained by solid state reaction at elevated temperature. Although both of the amorphous manganese oxides lack a long-range structural order, they are crystallized with a layered MnO2-type local structure, which is nearly identical to the crystal structure of the well-crystallized K0.45MnO2. In comparison with the well-crystallized K0.45MnO2, both the amorphous manganese oxides commonly possess smaller particle sizes with larger surface areas and better homogeneity of composite structure. The amorphous manganese oxide nanocrystals show better anode performance with greater discharge capacity for lithium ion batteries than does the well-crystallized K0.45MnO2, which is attributable to the greater surface area, higher structural and electrochemical stability, more homogeneous composite structure, and better charge-transfer characteristics of the amorphous materials. This result highlights the merit of the nanocrystalline and amorphous nature for optimizing the electrode performance of manganese oxide. The present solution-based redox reaction can provide a facile, economic, and scalable route for synthesizing efficient manganese

  15. Porous Nickel Oxide Film Sensor for Formaldehyde

    Science.gov (United States)

    Cindemir, U.; Topalian, Z.; Österlund, L.; Granqvist, C. G.; Niklasson, G. A.

    2014-11-01

    Formaldehyde is a volatile organic compound and a harmful indoor pollutant contributing to the "sick building syndrome". We used advanced gas deposition to fabricate highly porous nickel oxide (NiO) thin films for formaldehyde sensing. The films were deposited on Al2O3 substrates with prefabricated comb-structured electrodes and a resistive heater at the opposite face. The morphology and structure of the films were investigated with scanning electron microscopy and X-ray diffraction. Porosity was determined by nitrogen adsorption isotherms with the Brunauer-Emmett-Teller method. Gas sensing measurements were performed to demonstrate the resistive response of the sensors with respect to different concentrations of formaldehyde at 150 °C.

  16. Bacteria Absorption-Based Mn2P2O7-Carbon@Reduced Graphene Oxides for High-Performance Lithium-Ion Battery Anodes.

    Science.gov (United States)

    Yang, Yuhua; Wang, Bin; Zhu, Jingyi; Zhou, Jun; Xu, Zhi; Fan, Ling; Zhu, Jian; Podila, Ramakrishna; Rao, Apparao M; Lu, Bingan

    2016-05-24

    The development of freestanding flexible electrodes with high capacity and long cycle-life is a central issue for lithium-ion batteries (LIBs). Here, we use bacteria absorption of metallic Mn(2+) ions to in situ synthesize natural micro-yolk-shell-structure Mn2P2O7-carbon, followed by the use of vacuum filtration to obtain Mn2P2O7-carbon@reduced graphene oxides (RGO) papers for LIBs anodes. The Mn2P2O7 particles are completely encapsulated within the carbon film, which was obtained by carbonizing the bacterial wall. The resulting carbon microstructure reduces the electrode-electrolyte contact area, yielding high Coulombic efficiency. In addition, the yolk-shell structure with its internal void spaces is ideal for sustaining volume expansion of Mn2P2O7 during charge/discharge processes, and the carbon shells act as an ideal barrier, limiting most solid-electrolyte interphase formation on the surface of the carbon films (instead of forming on individual particles). Notably, the RGO films have high conductivity and robust mechanical flexibility. As a result of our combined strategies delineated in this article, our binder-free flexible anodes exhibit high capacities, long cycle-life, and excellent rate performance.

  17. Bacteria Absorption-Based Mn2P2O7-Carbon@Reduced Graphene Oxides for High-Performance Lithium-Ion Battery Anodes.

    Science.gov (United States)

    Yang, Yuhua; Wang, Bin; Zhu, Jingyi; Zhou, Jun; Xu, Zhi; Fan, Ling; Zhu, Jian; Podila, Ramakrishna; Rao, Apparao M; Lu, Bingan

    2016-05-24

    The development of freestanding flexible electrodes with high capacity and long cycle-life is a central issue for lithium-ion batteries (LIBs). Here, we use bacteria absorption of metallic Mn(2+) ions to in situ synthesize natural micro-yolk-shell-structure Mn2P2O7-carbon, followed by the use of vacuum filtration to obtain Mn2P2O7-carbon@reduced graphene oxides (RGO) papers for LIBs anodes. The Mn2P2O7 particles are completely encapsulated within the carbon film, which was obtained by carbonizing the bacterial wall. The resulting carbon microstructure reduces the electrode-electrolyte contact area, yielding high Coulombic efficiency. In addition, the yolk-shell structure with its internal void spaces is ideal for sustaining volume expansion of Mn2P2O7 during charge/discharge processes, and the carbon shells act as an ideal barrier, limiting most solid-electrolyte interphase formation on the surface of the carbon films (instead of forming on individual particles). Notably, the RGO films have high conductivity and robust mechanical flexibility. As a result of our combined strategies delineated in this article, our binder-free flexible anodes exhibit high capacities, long cycle-life, and excellent rate performance. PMID:27139149

  18. Facile Fabrication of Anodic Alumina Rod-Capped Nanopore Films with Condensate Microdrop Self-Propelling Function.

    Science.gov (United States)

    Li, Juan; Zhang, Wenjing; Luo, Yuting; Zhu, Jie; Gao, Xuefeng

    2015-08-26

    We report that aluminum surfaces can be endowed with condensate microdrop self-propelling (CMDSP) function by one-step voltage-rising mild anodization in hot phosphoric acid solution followed by fluorosilane modification. Via regulating reaction parameters, we can achieve anodic alumina self-standing rod-capped nanopore films and minimize their solid-liquid interface adhesion. Such low-adhesive nanostructured film owns remarkable CMDSP function, especially to condensate microdrops with sizes below 50 μm, differing from usual gravity-driven dropwise condensation on flat aluminum surfaces. Clearly, this work offers a facile, efficient, and industry-compatible approach to processing CMDSP aluminum materials, which is significant for developing innovative energy-saving air-conditioner heat exchangers.

  19. Photo-induced properties of non-annealed anatase TiO2 mesoporous film prepared by anodizing in the hot phosphate/glycerol electrolyte

    International Nuclear Information System (INIS)

    Highlights: ► The TiO2 mesoporous film can be formed by anodizing of titanium specimens in the hot phosphate/glycerol electrolyte. ► The mesoporous film formed at 20 V without annealing was a mixture of amorphous phase and nanograined anatase, which clearly showed strong 〈0 0 1〉 preferred orientation. ► Even without annealing, the as-anodized anatase TiO2 mesoporous film showed high photocatalytic activities for decomposition of water and methylene blue. ► The as-anodized anatase TiO2 mesoporous film also showed superhydrophilicity with UV light irradiation. - Abstract: In this study, anatase crystalline TiO2 mesoporous film was formed by anodizing of titanium specimens without annealing procedures. The specimens were anodized at 3 and 20 V in 0.6 mol dm−3 K2HPO4 and 0.2 mol dm−3 K3PO4/glycerol electrolyte at 433 K. The obtained films had mesoporous structures with pore diameters as small as ∼10 nm. The mesoporous film formed at 20 V without annealing (MP-20V) was a mixture of amorphous phase and nanograined anatase, which clearly showed strong 〈0 0 1〉 preferred orientation, whereas that at 3 V was completely amorphous. Even without annealing, the MP-20V showed high photocatalytic activities for decomposition of water and methylene blue. In contrast, the anodic TiO2 nanotube film formed in NH4F/ethylene glycol electrolyte revealed photocatalytic activities only after annealing at 723 K, because of the amorphous nature of the as-anodized nanotube film. The MP-20V film also showed superhydrophilicity with UV light irradiation.

  20. Water Clustering on Nanostructured Iron Oxide Films

    Energy Technology Data Exchange (ETDEWEB)

    Merte, L. R.; Bechstein, Ralf; Peng, Guowen; Rieboldt, Felix; Farberow, Carrie A.; Zeuthen, Helene; Knudsen, Jan; Laegsgaard, E.; Wendt, Stefen; Mavrikakis, Manos; Besenbacher, Fleming

    2014-06-30

    The adhesion of water to solid surfaces is characterized by the tendency to balance competing molecule–molecule and molecule–surface interactions. Hydroxyl groups form strong hydrogen bonds to water molecules and are known to substantially influence the wetting behaviour of oxide surfaces, but it is not well-understood how these hydroxyl groups and their distribution on a surface affect the molecular-scale structure at the interface. Here we report a study of water clustering on a moire´-structured iron oxide thin film with a controlled density of hydroxyl groups. While large amorphous monolayer islands form on the are film, the hydroxylated iron oxide film acts as a hydrophilic nanotemplate, causing the formation of a regular array of ice-like hexameric nanoclusters. The formation of this ordered phase is localized at the nanometre scale; with increasing water coverage, ordered and amorphous water are found to coexist at adjacent hydroxylated and hydroxyl-free domains of the moire´ structure.

  1. Water clustering on nanostructured iron oxide films

    Science.gov (United States)

    Merte, Lindsay R.; Bechstein, Ralf; Peng, Guowen; Rieboldt, Felix; Farberow, Carrie A.; Zeuthen, Helene; Knudsen, Jan; Lægsgaard, Erik; Wendt, Stefan; Mavrikakis, Manos; Besenbacher, Flemming

    2014-06-01

    The adhesion of water to solid surfaces is characterized by the tendency to balance competing molecule-molecule and molecule-surface interactions. Hydroxyl groups form strong hydrogen bonds to water molecules and are known to substantially influence the wetting behaviour of oxide surfaces, but it is not well-understood how these hydroxyl groups and their distribution on a surface affect the molecular-scale structure at the interface. Here we report a study of water clustering on a moiré-structured iron oxide thin film with a controlled density of hydroxyl groups. While large amorphous monolayer islands form on the bare film, the hydroxylated iron oxide film acts as a hydrophilic nanotemplate, causing the formation of a regular array of ice-like hexameric nanoclusters. The formation of this ordered phase is localized at the nanometre scale; with increasing water coverage, ordered and amorphous water are found to coexist at adjacent hydroxylated and hydroxyl-free domains of the moiré structure.

  2. Embedment of anodized p-type Cu₂O thin films with CuO nanowires for improvement in photoelectrochemical stability.

    Science.gov (United States)

    Wang, Peng; Ng, Yun Hau; Amal, Rose

    2013-04-01

    A highly stable p-type cuprous oxide (Cu2O) photoelectrode has been fabricated by direct anodization of the Cu foil, followed by a thermal treatment to introduce a protective layer of copper oxide (CuO) nanowires penetrating the surface of the Cu2O layer. The anodized Cu2O served as the seeding sites for the growth of CuO nanowires. The embedment of CuO nanowires within the Cu2O matrix enhanced the adhesion of the nanowires onto the Cu substrate. In addition, the presence of CuO nanowires on the outer layer of the composite film, in turn stabilized the Cu2O layer by passivating the redox activities of Cu2O when exposed to the environment. This nanostructured p-type Cu2O photoelectrode generated 360 μA cm(-2) of photocathodic current density upon visible light illumination and managed to retain its photocathodic current density after being used and kept for one month. The improvement in photoelectrochemical (PEC) stability by introducing a passive layer of CuO nanowires provides useful insights into the development of a Cu2O photoelectrode, as its stability remained as the main challenge.

  3. Degradation of 1-hydroxy-2,4-dinitrobenzene from aqueous solutions by electrochemical oxidation: role of anodic material.

    Science.gov (United States)

    Quiroz, Marco A; Sánchez-Salas, José L; Reyna, Silvia; Bandala, Erick R; Peralta-Hernández, Juan M; Martínez-Huitle, Carlos A

    2014-03-15

    Electrochemical oxidation (ECOx) of 1-hydroxy-2,4-dinitrobenzene (or 2,4-dinitrophenol: 2,4-DNP) in aqueous solutions by electrolysis under galvanostatic control was studied at Pb/PbO2, Ti/SnO2, Ti/IrxRuySnO2 and Si/BDD anodes as a function of current density applied. Oxidative degradation of 2,4-DNP has clearly shown that electrode material and the current density applied were important parameters to optimize the oxidation process. It was observed that 2,4-DNP was oxidized at few substrates to CO2 with different results, obtaining good removal efficiencies at Pb/PbO2, Ti/SnO2 and Si/BDD anodes. Trends in degradation way depend on the production of hydroxyl radicals (OH) on these anodic materials, as confirmed in this study. Furthermore, HPLC results suggested that two kinds of intermediates were generated, polyhydroxylated intermediates and carboxylic acids. The formation of these polyhydroxylated intermediates seems to be associated with the denitration step and substitution by OH radicals on aromatic rings, this being the first proposed step in the reaction mechanism. These compounds were successively oxidized, followed by the opening of aromatic rings and the formation of a series of carboxylic acids which were at the end oxidized into CO2 and H2O. On the basis of these information, a reaction scheme was proposed for each type of anode used for 2,4-D oxidation.

  4. Pulsed laser deposited Cr2O3 nanostructured thin film on graphene as anode material for lithium-ion batteries

    International Nuclear Information System (INIS)

    Graphical abstract: A different approach for the fabrication of an anode material system that comprises pulsed laser-deposited (PLD) Cr2O3 grown on few layer graphene (FLG) by chemical vapor deposition (CVD) was used. The electrochemical performance of Cr2O3 nanostructured thin film was improved by FLG, which make it a promising candidate for future lithium-ion batteries application. - Highlights: • Pulsed laser deposition technique was used to deposit Cr2O3 on few-layer graphene (FLG). • FLG improved the electrochemical performance of Cr2O3 nanostructured thin film. • Good stable cycle of Cr2O3/FLG/Ni electrode make it one of the promise anode materials for future lithium-ion batteries. - Abstract: Pulsed laser deposition technique was used to deposit Cr2O3 nanostructured thin film on a chemical vapor deposited few-layer graphene (FLG) on nickel (Ni) substrate for application as anode material for lithium-ion batteries. The experimental results show that graphene can effectively enhance the electrochemical property of Cr2O3. For Cr2O3 thin film deposited on Ni (Cr2O3/Ni), a discharge capacity of 747.8 mA h g−1 can be delivered during the first lithiation process. After growing Cr2O3 thin film on FLG/Ni, the initial discharge capacity of Cr2O3/FLG/Ni was improved to 1234.5 mA h g−1. The reversible lithium storage capacity of the as-grown material is 692.2 mA h g−1 after 100 cycles, which is much higher than that of Cr2O3/Ni (111.3 mA h g−1). This study reveals the differences between the two material systems and emphasizes the role of the graphene layers in improving the electrochemical stability of the Cr2O3 nanostructured thin film

  5. Anode materials for hydrogen sulfide containing feeds in a solid oxide fuel cell

    Science.gov (United States)

    Roushanafshar, Milad

    SOFCs which can directly operate under high concentration of H2S would be economically beneficial as this reduces the cost of gas purification. H2S is highly reactive gas specie which can poison most of the conventional catalysts. As a result, developing anode materials which can tolerate high concentrations of H2S and also display high activity toward electrochemical oxidation of feed is crucial and challenging for this application. The performance of La0.4Sr0.6TiO3+/-delta -Y0.2Ce0.8O2-delta (LST-YDC) composite anodes in solid oxide fuel cells significantly improved when 0.5% H2 S was present in syngas (40% H2, 60% CO) or hydrogen. Gas chromatography and mass spectrometry analyses revealed that the rate of electrochemical oxidation of all fuel components improved when H2S containing syngas was present in the fuel. Electrochemical stability tests performed under potentiostatic condition showed that there was no power degradation for different feeds, and that there was power enhancement when 0.5% H2S was present in various feeds. The mechanism of performance improvement by H2S was discussed. Active anodes were synthesized via wet chemical impregnation of different amounts of La0.4Ce0.6O1.8 (LDC) and La 0.4Sr0.6TiO3 (L4ST) into porous yttria-stabilized zirconia (YSZ). Co-impregnation of LDC with LS4T significantly improved the performance of the cell from 48 mW.cm-2 (L4ST) to 161 mW.cm -2 (LDC-L4ST) using hydrogen as fuel at 900 °C. The contribution of LDC to this improvement was investigated using electrochemical impedance spectroscopy (EIS), scanning electron microscopy (SEM) as well as transmission electron microscopy (TEM). EIS measurements using symmetrical cells showed that the polarization resistance decreased from 3.1¦O.cm 2 to 0.5 O.cm2 when LDC was co-impregnated with LST, characterized in humidified H2 (3% H2O) at 900 °C. In addition, the microstructure of the cell was modified when LDC was impregnated prior to L4ST into the porous YSZ. TEM and SEM

  6. Study on the mechanism of the anodization of niobium by using ion-implanting Xe+ markers and RBS analysis

    International Nuclear Information System (INIS)

    The mechanism of anodic oxidation on niobium in the solution of aqueous ammonium citrate (w = 5%) was studied with the layers of ion-implanted Xe atom markers in different depth and analysed by the methods of RBS, X-ray and AES and the ions migration numbers under different anodic potentials were calculated. The main reason for the forming of oxide films is the migration of both metal cations and oxygen anions in contrary directions and the area in which the oxide film formed is nearer the sample surface, which is connected with the solution, with the higher anodic potential. The composition of the oxide film is Nb2O5

  7. Cytocompatibility of titanium metal injection molding with various anodic oxidation post-treatments

    International Nuclear Information System (INIS)

    Metal injection molding (MIM) is a near net shape manufacturing method that allows for the production of components of small to moderate size and complex shape. MIM is a cost-effective and flexible manufacturing technique that provides a large innovative potential over existing methods for the industry of implantable devices. Commercially pure titanium (CP-Ti) samples were machined to the same shape as a composite feedstock with titanium and polyoxymethylene, and these metals were injected, debinded and sintered to assess comparative biological properties. Moreover, we treated MIM-Ti parts with BIOCOAT®, BIODIZE® and BIOCER®, three different anodic oxidation techniques that treat titanium using acid, alkaline and anion enriched electrolytes, respectively. Cytocompatibility as well as morphological and chemical features of surfaces was comparatively assessed on each sample, and the results revealed that MIM-Ti compared to CP-Ti demonstrated a specific surface topography with a higher roughness. MIM-Ti and BIOCER® samples significantly enhanced cell proliferation, cell adhesion and cell differentiation compared to CP-Ti. Interestingly, in the anodization post-treatment established in this study, we demonstrated the ability to improve osseointegration through anionic modification treatment. The excellent biological response we observed with MIM parts using the injection molding process represents a promising manufacturing method for the future implantable devices in direct contact with bones. - Highlights: ► Metal injection molding technique gives titanium a specific surface roughness. It enhances the biological response. ► Anodic oxidation method adds Ca, P, and Mg ions on the surface, promoting the cell adhesion. ► Cytocompatibility analyses show an increased cell adhesion and proliferation on MIM-Ti compared to pure titanium.

  8. Investigation into the diffusion and oxidation behavior of the interface between a plasma-sprayed anode and a porous steel support for solid oxide fuel cells

    Science.gov (United States)

    Zhang, Shan-Lin; Li, Cheng-Xin; Li, Chang-Jiu; Liu, Meilin; Yang, Guan-Jun

    2016-08-01

    Porous metal-supported solid oxide fuel cells (SOFCs) have attracted much attention because their potential to dramatically reduce the cost while enhancing the robustness and manufacturability. In particular, 430 ferritic steel (430L) is one of the popular choice for SOFC support because of its superior performance and low cost. In this study, we investigate the oxidation and diffusion behavior of the interface between a Ni-based anode and porous 430L support exposed to a humidified (3% H2O) hydrogen atmosphere at 700 °C. The Ni-GDC (Ce0.8Gd0.2O2-δ) cermet anodes are deposited on the porous 430L support by atmospheric plasma spraying (APS). The effect of exposure time on the microstructure and phase structure of the anode and the supports is studied and the element diffusion across the support/anode interface is characterized. Results indicate that the main oxidation product of the 430L support is Cr2O3, and that Cr and Fe will diffuse to the anode and the diffusion thickness increases with the exposure time. The diffusion thickness of Cr and Fe reach about 5 and 2 μm, respectively, after 1000 h exposure. However, the element diffusion and oxidation has little influence on the area-specific resistance, indicating that the porous 430L steel and plasma sprayed Ni-GDC anode are promising for durable SOFCs.

  9. Epitaxial copper oxide thin films deposited on cubic oxide substrates

    International Nuclear Information System (INIS)

    We study the growth conditions of Cu2O thin films deposited on MgO (0 0 1) and SrTiO3 (0 0 1) substrates by pulsed laser ablation, in order to explore the compatibility between semiconducting p-type Cu2O and other perovskite oxides in view of the fabrication of oxide electronics heterostructures. We find that in both cases perfect epitaxy, high crystalline quality and good out-of-plane orientation are achieved. In this context, epitaxy plays a major role in driving the phase formation. On the other hand, in films deposited at temperatures higher than 700 deg. C transport is inhibited by poor grain connectivity, which is an inevitable consequence of the necessity for the crystal to release the lattice strain. Instead, better connectivity and bulk-like values of resistivity, as well as good crystallinity and orientation, are obtained for films deposited at 650 deg. C. This should be kept in mind for the fabrication of stacked layer oxide heterostructures, where deep grooves between adjacent grains would be a serious drawback both for vertical and planar transport

  10. Anodic aluminum oxide with fine pore size control for selective and effective particulate matter filtering

    Science.gov (United States)

    Zhang, Su; Wang, Yang; Tan, Yingling; Zhu, Jianfeng; Liu, Kai; Zhu, Jia

    2016-07-01

    Air pollution is widely considered as one of the most pressing environmental health issues. Particularly, atmospheric particulate matters (PM), a complex mixture of solid or liquid matter suspended in the atmosphere, are a harmful form of air pollution due to its ability to penetrate deep into the lungs and blood streams, causing permanent damages such as DNA mutations and premature death. Therefore, porous materials which can effectively filter out particulate matters are highly desirable. Here, for the first time, we demonstrate that anodic aluminum oxide with fine pore size control fabricated through a scalable process can serve as effective and selective filtering materials for different types of particulate matters (such as PM2.5, PM10). Combining selective and dramatic filtering effect, fine pore size control and a scalable process, this type of anodic aluminum oxide templates can potentially serve as a novel selective filter for different kinds of particulate matters, and a promising and complementary solution to tackle this serious environmental issue.

  11. Electrochemical oxidation of biological pretreated and membrane separated landfill leachate concentrates on boron doped diamond anode

    Science.gov (United States)

    Zhou, Bo; Yu, Zhiming; Wei, Qiuping; Long, HangYu; Xie, Youneng; Wang, Yijia

    2016-07-01

    In the present study, the high quality boron-doped diamond (BDD) electrodes with excellent electrochemical properties were deposited on niobium (Nb) substrates by hot filament chemical vapor deposition (HFCVD) method. The electrochemical oxidation of landfill leachate concentrates from disc tube reverse osmosis (DTRO) process over a BDD anode was investigated. The effects of varying operating parameters, such as current density, initial pH, flow velocity and cathode material on degradation efficiency were also evaluated following changes in chemical oxygen demand (COD) and ammonium nitrogen (NH3sbnd N). The instantaneous current efficiency (ICE) was used to appraise different operating conditions. As a result, the best conditions obtained were as follows, current density 50 mA cm-2, pH 5.16, flow velocity 6 L h-1. Under these conditions, 87.5% COD and 74.06% NH3sbnd N removal were achieved after 6 h treatment, with specific energy consumption of 223.2 kWh m-3. In short, these results indicated that the electrochemical oxidation with BDD/Nb anode is an effective method for the treatment of landfill leachate concentrates.

  12. Infiltrated lanthanum strontium chromite anodes for solid oxide fuel cells: Structural and catalytic aspects

    Science.gov (United States)

    Oh, Tae-Sik; Yu, Anthony S.; Adijanto, Lawrence; Gorte, Raymond J.; Vohs, John M.

    2014-09-01

    Infiltration is a widely used fabrication method for solid oxide fuel cell (SOFC) composite electrodes. Here we report a study of the structure and electrocatalytic properties of SOFC anodes composed of a layer of lanthanum, strontium chromite (La0.8Sr0.2CrO3, LSCr), both with and without added transition metal dopants, infiltrated into a porous yttria-stabilized zirconia (YSZ) matrix. The structural evolution of the electrode upon reduction and under typical SOFC operating conditions is compared to that reported previously for La0.8Sr0.2Cr0.5Mn0.5O3-YSZ composite anodes. For the transition metal doped materials, a portion of the metal dopants were found to be exsolved from the LSCr lattice upon reduction and to be effective in promoting electro-oxidation of hydrogen. Exsolved cobalt particles were also found to be relatively stable when exposed to hydrocarbon fuels with low activity for the formation of carbon deposits.

  13. Understanding the interfacial phenomena of a 4.7 V and 55 °C Li-ion battery with Li-rich layered oxide cathode and grap2hite anode and its correlation to high-energy cycling performance

    Science.gov (United States)

    Pham, Hieu Quang; Hwang, Eui-Hyung; Kwon, Young-Gil; Song, Seung-Wan

    2016-08-01

    Research progress of high-energy performance and interfacial phenomena of Li1.13Mn0.463Ni0.203Co0.203O2 cathode and graphite anode in a 55 °C full-cell under an aggressive charge cut-off voltage to 4.7 V (4.75 V vs. Li/Li+) is reported. Although anodic instability of conventional electrolyte is the critical issue on high-voltage and high-temperature cell operation, interfacial phenomena and the solution to performance improvement have not been reported. Surface spectroscopic evidence revealed that structural degradation of both cathode and anode materials, instability of surface film at cathode, and metal-dissolution from cathode and -deposition at anode, and a rise of interfacial resistance with high-voltage cycling in 55 °C conventional electrolyte are resolved by the formation of a stable surface film with organic/inorganic mixtures at cathode and solid electrolyte interphase (SEI) at anode using blended additives of fluorinated linear carbonate and vinylene carbonate. As a result, significantly improved cycling stability of 77% capacity retention delivering 227-174 mAhg-1 after 50 cycles is obtained, corresponding to 819-609 Wh per kg of cathode active material. Interfacial stabilization approach would pave the way of controlling the performance and safety, and widening the practical application of Li-rich layered oxide cathode materials and high-voltage electrolyte materials in various high-energy density Li-ion batteries.

  14. Simultaneous Use Of Zr And Mg Anodes In XPS

    Science.gov (United States)

    Allgeyer, D. F.; Pratz, E. H.

    1996-01-01

    Improved x-ray source for x-ray photoelectron spectroscopy (XPS) contains both zirconium anode with beryllium window and magnesium anode with aluminum window. Previously unresolvable peaks of electron-energy spectrum become resolvable. Developed specifically for use in analyzing distributions of chemical constituents in surface layers of specimens of 2219 aluminum alloy and in determining the depths of surface oxide layers and relative proportions of aluminum and oxide in layers. Also used to study chemical constituents of surface layers in other material systems - for example, thin oxide films on silicon-based semiconductor devices, oxide films on alloys, and surface layers affecting adhesion of paints or bonding materials.

  15. Effect of electrolyte temperature on the thickness of anodic aluminium oxide (AAO layer

    Directory of Open Access Journals (Sweden)

    P. Michal

    2016-07-01

    Full Text Available Effect of electrolyte temperature on the thickness of resulting oxide layer has been studied. Unlike previous published studies this article was aimed to monitor the relationship between electrolyte temperature and resulting AAO layer thickness in interaction with other input factors affecting during anodizing process under special process condition, i.e. lower concentration of sulphuric acid, oxalic acid, boric acid and sodium chloride. According to Design of Experiments (DOE 80 individual test runs of experiment were carried out. Using statistical analysis and artificial intelligence for evaluation, the computational model predicting the thickness of oxide layer in the range from 5 / μm to 15 / μm with tolerance ± 0,5 / μm was developed.

  16. Titanium oxide layers on aluminium substrates produced by the anodic spark deposition process

    International Nuclear Information System (INIS)

    Titanium oxide layers were prepared on pure aluminium substrates by the anodic spark deposition method. The formed crystalline titania (TiO2) phases rutile and anatase and the sodium titanium oxide (Na0.23TiO2) were identified. The corresponding crystallite size values were obtained from X-ray diffraction data by means of the Rietveld method. The crystallite size of each of these phases continuously increases with rising current density. Furthermore, the two-dimensional distribution of the titania phases on the sample surface was determined by Raman spectroscopy. It was found that the rutile/anatase ratio is inhomogeneous distributed on an observed area of 400 x 400 μm2.

  17. Effects of sodium tartrate anodizing on fatigue life of TA15 titanium alloy

    Directory of Open Access Journals (Sweden)

    Fu Chunjuan

    2015-08-01

    Full Text Available Anodizing is always used as an effective surface modification method to improve the corrosion resistance and wear resistance of titanium alloy. The sodium tartrate anodizing is a new kind of environmental anodizing method. In this work, the effects of sodium tartrate anodizing on mechanical property were studied. The oxide film was performed on the TA15 titanium alloy using sodium tartrate as the film former. The effects of this anodizing and the traditional acid anodizing on the fatigue life of TA15 alloy were compared. The results show that the sodium tartrate anodizing just caused a slight increase of hydrogen content in the alloy, and had a slight effect on the fatigue life. While, the traditional acid anodizing caused a significant increase of hydrogen content in the substrate and reduced the fatigue life of the alloy significantly.

  18. Performance Factors and Sulfur Tolerance of Metal Supported Solid Oxide Fuel Cells with Nanostructured Ni:GDC Infiltrated Anodes

    DEFF Research Database (Denmark)

    Nielsen, Jimmi; Sudireddy, Bhaskar Reddy; Hagen, Anke;

    2015-01-01

    Two metal supported solid oxide fuel cells (active area 16 cm2) with nanostructured Ni:GDC infiltrated anodes, but different anode and support microstructures were studied in respect to sulfur tolerance at the aimed operating temperature of 650ºC. The studied MS-SOFCs are based on ferretic stainl...... anode is significantly more sulfur tolerant than the conventional Ni/YSZ cermet anode. © 2015 ECS - The Electrochemical Society......Two metal supported solid oxide fuel cells (active area 16 cm2) with nanostructured Ni:GDC infiltrated anodes, but different anode and support microstructures were studied in respect to sulfur tolerance at the aimed operating temperature of 650ºC. The studied MS-SOFCs are based on ferretic...... stainless steel (FeCr) and showed excellent performance characteristics at 650ºC with area specific resistances (ASR) of 0.35 Ωcm2 and 0.7 Ωcm2 respectively. The sulfur tolerance testing was performed by addition/removal of 2, 5, and 10 ppm H2S in hydrogen based fuel under galvanostatic operation...

  19. Performance Factors and Sulfur Tolerance of Metal Supported Solid Oxide Fuel Cells with Nanostructured Ni:GDC Infiltrated Anodes

    DEFF Research Database (Denmark)

    Nielsen, Jimmi; Sudireddy, Bhaskar Reddy; Hagen, Anke;

    2016-01-01

    Two metal supported solid oxide fuel cells (active area 16 cm2) with nanostructured Ni:GDC infiltrated anodes, possessing different anode and support microstructures were studied in respect to sulfur tolerance at an operating temperature of 650°C. The studied MS-SOFCs are based on ferretic...... stainless steel (FeCr) and showed excellent performance characteristics at 650°C with fuel utilization corrected area specific resistances of 0.35 Ωcm2 and 0.7 Ωcm2 respectively. The sulfur tolerance testing was performed by periodic addition of 2, 5, and 10 ppm H2S in hydrogen based fuel under...... galvanostatic operation at a current load of 0.25 Acm−2. The results were compared with literature on the sulfur tolerance of conventional SOFC Ni/YSZ cermet anode. The comparison in terms of absolute cell resistance increase and relative anode polarization resistance increase indicates, that the nanostructured...

  20. Ni coarsening in the three-phase solid oxide fuel cell anode - a phase-field simulation study

    CERN Document Server

    Chen, Hsun-Yi; Cronin, J Scott; Wilson, James R; Barnett, Scott A; Thornton, Katsuyo

    2012-01-01

    Ni coarsening in Ni-yttria stabilized zirconia (YSZ) solid oxide fuel cell anodes is considered a major reason for anode degradation. We present a predictive, quantative modeling framework based on the phase-field approach to systematically examine coarsening kinetics in such anodes. The initial structures for simulations are experimentally acquired functional layers of anodes. Sample size effects and error analysis of contact angles are examined. Three phase boundary (TPB) lengths and Ni surface areas are quantatively identified on the basis of the active, dead-end, and isolated phase clusters throughout coarsening. Tortuosity evolution of the pores is also investigated. We find that phase clusters with larger characteristic length evolve slower than those with smaller length scales. As a result, coarsening has small positive effects on transport, and impacts less on the active Ni surface area than the total counter part. TPBs, however, are found to be sensitive to local morphological features and are only i...

  1. Highly Transparent and Flexible Triboelectric Nanogenerators with Subwavelength-Architectured Polydimethylsiloxane by a Nanoporous Anodic Aluminum Oxide Template.

    Science.gov (United States)

    Dudem, Bhaskar; Ko, Yeong Hwan; Leem, Jung Woo; Lee, Soo Hyun; Yu, Jae Su

    2015-09-23

    Highly transparent and flexible triboelectric nanogenerators (TENGs) were fabricated using the subwavelength-architectured (SWA) polydimethylsiloxane (PDMS) with a nanoporous anodic aluminum oxide (AAO) template as a replica mold. The SWA PDMS could be utilized as a multifunctional film for a triboelectric layer, an antireflection coating, and a self-cleaning surface. The nanopore arrays of AAO were formed by a simple, fast, and cost-effective electrochemical oxidation process of aluminum, which is relatively impressive for fabrication of the TENG device. For electrical contacts, the SWA PDMS was laminated on the indium tin oxide (ITO)-coated polyethylene terephthalate (PET) as a bottom electrode, and the bare ITO-coated PET (i.e., ITO/PET) was used for the top electrode. Compared to the ITO/PET, the SWA PDMS on the ITO/PET improved the transmittance from 80.5 to 83% in the visible wavelength region and also had high transmittances of >85% at wavelengths of 430-455 nm. The SWA PDMS also exhibited the hydrophobic surface with a water contact angle (θCA) of ∼115°, which can be useful for self-cleaning applications. The average transmittance (Tavg) of the entire TENG device was observed to be ∼70% over a broad wavelength range. At an external pushing frequency of 0.5 Hz, for the TENG device with the ITO top electrode, open-circuit voltage (VOC) and short-circuit current (ISC) values of ∼3.8 V and ∼0.8 μA were obtained instantaneously, respectively, which were higher than those (i.e., VOC ≈ 2.2 V, and ISC ≈ 0.4 μA) of the TENG device with a gold top electrode. The effect of external pushing force and frequency on the output device performance of the TENGs was investigated, including the device robustness. A theoretical optical analysis of SWA PDMS was also performed. PMID:26301328

  2. Nickel oxide sol-gel films from nickel diacetate for electrochromic applications

    International Nuclear Information System (INIS)

    Nickel diacetate tetrahydrate, [Ni(acetate)2·4H2O] and nickel diacetate dimethylaminoethanol, [Ni(acetate)2(dmaeH)2] were successfully used to deposit NiOx thin films on conductive glass substrates by sol-gel techniques for large area electrochromic applications. Homogeneous one layer films 100 nm thick were deposited by spin coating 0.5 M [Ni(acetate)2·4H2O] in dmaeH at 1000 rpm and by dip coating methods. The NiOx films were characterised by X-ray diffraction, transmission electron microscopy and atomic force microscopy. The thin film electrochromic performances were characterised by means of optical (transmittance) and electrochemical (cyclic voltammetry) methods. On early cycling NiOx thin films present an activation period, related to an increase in capacity. The electro-optical data show an increase in the electrochromic response (i.e. an increase in contrast and colouration efficiency) upon cycling. Following this initial activation period a steady state is reached in which the thin films reversibly switch from transparent to brown. The anodically coloured NiOx thin films are therefore suitable for use in a complete electrochromic cell with tungsten oxide as the cathodic colouring layer. However, the films are not fully stable with long cycling

  3. Nickel oxide sol-gel films from nickel diacetate for electrochromic applications

    Energy Technology Data Exchange (ETDEWEB)

    Garcia-Miquel, J.L.; Zhang, Q.; Allen, S.J.; Rougier, A.; Blyr, A.; Davies, H.O.; Jones, A.C.; Leedham, T.J.; Williams, P.A.; Impey, S.A

    2003-01-31

    Nickel diacetate tetrahydrate, [Ni(acetate){sub 2}{center_dot}4H{sub 2}O] and nickel diacetate dimethylaminoethanol, [Ni(acetate){sub 2}(dmaeH){sub 2}] were successfully used to deposit NiO{sub x} thin films on conductive glass substrates by sol-gel techniques for large area electrochromic applications. Homogeneous one layer films 100 nm thick were deposited by spin coating 0.5 M [Ni(acetate){sub 2}{center_dot}4H{sub 2}O] in dmaeH at 1000 rpm and by dip coating methods. The NiO{sub x} films were characterised by X-ray diffraction, transmission electron microscopy and atomic force microscopy. The thin film electrochromic performances were characterised by means of optical (transmittance) and electrochemical (cyclic voltammetry) methods. On early cycling NiO{sub x} thin films present an activation period, related to an increase in capacity. The electro-optical data show an increase in the electrochromic response (i.e. an increase in contrast and colouration efficiency) upon cycling. Following this initial activation period a steady state is reached in which the thin films reversibly switch from transparent to brown. The anodically coloured NiO{sub x} thin films are therefore suitable for use in a complete electrochromic cell with tungsten oxide as the cathodic colouring layer. However, the films are not fully stable with long cycling.

  4. Ceria-Based Anodes for Next Generation Solid Oxide Fuel Cells

    Science.gov (United States)

    Mirfakhraei, Behzad

    Mixed ionic and electronic conducting materials (MIECs) have been suggested to represent the next generation of solid oxide fuel cell (SOFC) anodes, primarily due to their significantly enhanced active surface area and their tolerance to fuel components. In this thesis, the main focus has been on determining and tuning the physicochemical and electrochemical properties of ceria-based MIECs in the versatile perovskite or fluorite crystal structures. In one direction, BaZr0.1Ce0.7Y0.1 M0.1O3-delta (M = Fe, Ni, Co and Yb) (BZCY-M) perovskites were synthesized using solid-state or wet citric acid combustion methods and the effect of various transition metal dopants on the sintering behavior, crystal structure, chemical stability under CO2 and H 2S, and electrical conductivity, was investigated. BZCY-Ni, synthesized using the wet combustion method, was the best performing anode, giving a polarization resistance (RP) of 0.4 O.cm2 at 800 °C. Scanning electron microscopy and X-ray diffraction analysis showed that this was due to the exsolution of catalytic Ni nanoparticles onto the oxide surface. Evolving from this promising result, the effect of Mo-doped CeO 2 (nCMO) or Ni nanoparticle infiltration into a porous Gd-doped CeO 2 (GDC) anode (in the fluorite structure) was studied. While 3 wt. % Ni infiltration lowered RP by up to 90 %, giving 0.09 O.cm2 at 800 °C and exhibiting a ca. 5 times higher tolerance towards 10 ppm H2, nCMO infiltration enhanced the H2 stability by ca. 3 times, but had no influence on RP. In parallel work, a first-time study of the Ce3+ and Ce 4+ redox process (pseudocapacitance) within GDC anode materials was carried out using cyclic voltammetry (CV) in wet H2 at high temperatures. It was concluded that, at 500-600 °C, the Ce3+/Ce 4+ reaction is diffusion controlled, probably due to O2- transport limitations in the outer 5-10 layers of the GDC particles, giving a very high capacitance of ca. 70 F/g. Increasing the temperature ultimately

  5. Flame oxidation of stainless steel felt enhances anodic biofilm formation and current output in bioelectrochemical systems.

    Science.gov (United States)

    Guo, Kun; Donose, Bogdan C; Soeriyadi, Alexander H; Prévoteau, Antonin; Patil, Sunil A; Freguia, Stefano; Gooding, J Justin; Rabaey, Korneel

    2014-06-17

    Stainless steel (SS) can be an attractive material to create large electrodes for microbial bioelectrochemical systems (BESs), due to its low cost and high conductivity. However, poor biocompatibility limits its successful application today. Here we report a simple and effective method to make SS electrodes biocompatible by means of flame oxidation. Physicochemical characterization of electrode surface indicated that iron oxide nanoparticles (IONPs) were generated in situ on an SS felt surface by flame oxidation. IONPs-coating dramatically enhanced the biocompatibility of SS felt and consequently resulted in a robust electroactive biofilm formation at its surface in BESs. The maximum current densities reached at IONPs-coated SS felt electrodes were 16.5 times and 4.8 times higher than the untreated SS felts and carbon felts, respectively. Furthermore, the maximum current density achieved with the IONPs-coated SS felt (1.92 mA/cm(2), 27.42 mA/cm(3)) is one of the highest current densities reported thus far. These results demonstrate for the first time that flame oxidized SS felts could be a good alternative to carbon-based electrodes for achieving high current densities in BESs. Most importantly, high conductivity, excellent mechanical strength, strong chemical stability, large specific surface area, and comparatively low cost of flame oxidized SS felts offer exciting opportunities for scaling-up of the anodes for BESs.

  6. Tin doped indium oxide anodes with artificially controlled nano-scale roughness using segregated Ag nanoparticles for organic solar cells.

    Science.gov (United States)

    Kim, Hyo-Joong; Ko, Eun-Hye; Noh, Yong-Jin; Na, Seok-In; Kim, Han-Ki

    2016-01-01

    Nano-scale surface roughness in transparent ITO films was artificially formed by sputtering a mixed Ag and ITO layer and wet etching of segregated Ag nanoparticles from the surface of the ITO film. Effective removal of self-segregated Ag particles from the grain boundaries and surface of the crystalline ITO film led to a change in only the nano-scale surface morphology of ITO film without changes in the sheet resistance and optical transmittance. A nano-scale rough surface of the ITO film led to an increase in contact area between the hole transport layer and the ITO anode, and eventually increased the hole extraction efficiency in the organic solar cells (OSCs). The heterojunction OSCs fabricated on the ITO anode with a nano-scale surface roughness exhibited a higher power conversion efficiency of 3.320%, than that (2.938%) of OSCs made with the reference ITO/glass. The results here introduce a new method to improve the performance of OSCs by simply modifying the surface morphology of the ITO anodes. PMID:27640723

  7. Fabrication of SERS-active substrates using silver nanofilm-coated porous anodic aluminum oxide for detection of antibiotics.

    Science.gov (United States)

    Chen, Jing; Feng, Shaolong; Gao, Fang; Grant, Edward; Xu, Jie; Wang, Shuo; Huang, Qian; Lu, Xiaonan

    2015-04-01

    We have developed a silver nanofilm-coated porous anodic aluminum oxide (AAO) as a surface-enhanced Raman scattering (SERS)-active substrate for the detection of trace level of chloramphenicol, a representative antibiotic in food systems. The ordered aluminum template generated during the synthesis of AAO serves as a patterned matrix on which a coated silver film replicates the patterned AAO matrix to form a 2-dimensional ordered nanostructure. We used atomic force microscopy and scanning electron microscopy images to determine the morphology of this nanosubstrate, and characterized its localized surface plasmon resonance by ultraviolet-visible reflection. We gauged the SERS effect of this nanosubstrate by confocal micro-Raman spectroscopy (782-nm laser), finding a satisfactory and consistent performance with enhancement factors of approximately 2 × 10(4) and a limit of detection for chloramphenicol of 7.5 ppb. We applied principal component analysis to determine the limit of quantification for chloramphenicol of 10 ppb. Using electromagnetic field theory, we developed a detailed mathematical model to explain the mechanism of Raman signal enhancement of this nanosubstrate. With simple sample pretreatment and separation steps, this silver nanofilm-coated AAO substrate could detect 50 ppb chloramphenicol in milk, indicating good potential as a reliable SERS-active substrate for rapid detection of chemical contaminants in agricultural and food products.

  8. Influence of wet etching time cycles on morphology features of thin porous Anodic Aluminum oxide (AAO) template for nanostructure's synthesis

    Science.gov (United States)

    Chahrour, Khaled M.; Ahmed, Naser M.; Hashim, M. R.; Elfadill, Nezar G.; Al-Diabat, Ahmad M.; Bououdina, M.

    2015-12-01

    This study examines the influence of chemical wet etching time cycles on the morphological features of thin porous AAO template. Pore widening via wet-etching treatment at room temperature was found to modify the pore quality of AAO template and reduces the barrier layer on the bottom of AAO pore array in order to facilitate uniform electrodeposition of nanostructures onto AAO template. High quality AAO pore arrays with different mean pore diameters (64, 70, and 87 nm) were prepared under controllable pore-widening time cycles of 10, 30 and 45 min at room temperature, respectively. The AAO templates and the produced Cu nanorods were characterized using FESEM, EDX, XRD and AFM. The results indicate that the morphology of the aligned arrays of Cu nanorods is strongly affected by the duration of etching and the removal of AAO template. This study showed that the optimum etching duration required to maintain the aligned nanorods without any fracture is approximately 5 min. In addition, the regular hemispherical concave Al surface ensuring the self-ordering of AAO pore can be established when striping is employed for 45 min. Thus, it can be inferred that the duration of wet etching treatment (striping) of Al oxide film performed after the first-step anodization plays a vital role in the final arrangement of nanopores.

  9. A Macroporous TiO2 Oxygen Sensor Fabricated Using Anodic Aluminium Oxide as an Etching Mask

    Directory of Open Access Journals (Sweden)

    Sheng-Po Wu

    2010-01-01

    Full Text Available An innovative fabrication method to produce a macroporous Si surface by employing an anodic aluminium oxide (AAO nanopore array layer as an etching template is presented. Combining AAO with a reactive ion etching (RIE processes, a homogeneous and macroporous silicon surface can be effectively configured by modulating AAO process parameters and alumina film thickness, thus hopefully replacing conventional photolithography and electrochemical etch methods. The hybrid process integration is considered fully CMOS compatible thanks to the low-temperature AAO and CMOS processes. The gas-sensing characteristics of 50 nm TiO2 nanofilms deposited on the macroporous surface are compared with those of conventional plain (or non-porous nanofilms to verify reduced response noise and improved sensitivity as a result of their macroporosity. Our experimental results reveal that macroporous geometry of the TiO2 chemoresistive gas sensor demonstrates 2-fold higher (~33% improved sensitivity than a non-porous sensor at different levels of oxygen exposure. In addition, the macroporous device exhibits excellent discrimination capability and significantly lessened response noise at 500 °C. Experimental results indicate that the hybrid process of such miniature and macroporous devices are compatible as well as applicable to integrated next generation bio-chemical sensors.

  10. Effective improvement of interface modified strontium titanate based solid oxide fuel cell anodes by infiltration with nano-sized palladium and gadolinium-doped cerium oxide

    DEFF Research Database (Denmark)

    Abdul Jabbar, Mohammed Hussain; Høgh, Jens Valdemar Thorvald; Zhang, Wei;

    2013-01-01

    The development of low temperature solid oxide fuel cell (SOFC) anodes by infiltration of Pd/Gd-doped cerium oxide (CGO) electrocatalysts in Nb-doped SrTiO3 (STN) backbones has been investigated. Modification of the electrode/electrolyte interface by thin layer of spin-coated CGO (400-500 nm) con...

  11. An investigation of oxide composite anode materials for lithium ion batteries

    Science.gov (United States)

    Liu, Bo

    This thesis is aimed to develop high-capacity, inexpensive, long cycle life and environmentally benign anode for lithium-ion batteries. With those goals in mind, a novel oxide alloy composite materials MO-Sn xCoyCz (MO=GeO2, SnO2, SiO and SiO2) have been proposed and investigated. Mechanical alloying method has been used to synthesize oxide alloy composite anode material. The MO-SnxCo yCz composite has the potential to combine the advantageous properties of both Sn-Co-C (long cycle life) and MO (high capacity) and, thereby, improve the overall electrochemical performance. The as-milled materials were studied by BET, laser particle analyzer, X-ray diffraction (XRD), scanning electron microscope (SEM), pair distribution function (PDF), extended X-ray absorption fine structure (EXAFS). Evaluating from electrochemical performance, tap density, and cost, GeO2 and SiO are the most promising candidates alloyed with Sn-Co-C system. The GeO 2 composite anode shows a reversible capacity over 800 mAh/g with good capacity retention. Furthermore, the 1st cycle coulombic efficiency has been improved up to 80%. Compared with GeO2, SiO has an advantage on the price. A series of composite anode materials of xSiO * (1-x)SnxCoyC z were studied by electrochemical method. The composition of 50 wt.%SiO-50 wt.%Sn30Co30C40 shows the best electrochemical performance. Two different milling methods (ultra high-energy milling and SPEX milling) were employed to prepare the samples. Ultra high-energy milling sample exhibited superior electrochemical performance. Stabilized lithium metallic powder technique is employed on this anode to improve the first cycle coulombic efficiency. Full-cell configuration (Li1.2Ni 0.15Co0.10Mn0.55O2 vs. 50 wt.%SiO-50 wt.% Sn30Co30C40) has been cycled over 200 cycles successfully. The SiO-SnxFeyC z (x : y: z molar ratio) composite has been milled in different compositions. Metallic iron was employed instead of cobalt, which cuts the cost significantly but does not

  12. Copper oxide thin films for ethanol sensing

    Science.gov (United States)

    Lamri Zeggar, M.; Bourfaa, F.; Adjimi, A.; Aida, M. S.; Attaf, N.

    2016-03-01

    The present is a study of a new active layer for ethanol (C2H5OH) vapour sensing devices based on copper oxide (CuO). CuO films were prepared by spray ultrasonic pyrolysis at a substrate temperature of 350 °C. Films microstructure was examined by X-ray diffraction and atomic force microscopy. Vapour-sensing testing was conducted using static vapour-sensing system, at different operating temperatures in the range of 100°C to 175°C for the vapour concentration of 300 ppm. The results show a high response of 45% at relatively low operating temperatures of 150°C towards ethanol vapour.

  13. Effect of Samarium Oxide on the Electrical Conductivity of Plasma-Sprayed SOFC Anodes

    Science.gov (United States)

    Panahi, S. N.; Samadi, H.; Nemati, A.

    2016-05-01

    Solid oxide fuel cells (SOFCs) are rapidly becoming recognized as a new alternative to traditional energy conversion systems because of their high energy efficiency. From an ecological perspective, this environmentally friendly technology, which produces clean energy, is likely to be implemented more frequently in the future. However, the current SOFC technology still cannot meet the demands of commercial applications due to temperature constraints and high cost. To develop a marketable SOFC, suppliers have tended to reduce the operating temperatures by a few hundred degrees. The overall trend for SOFC materials is to reduce their service temperature of electrolyte. Meanwhile, it is important that the other components perform at the same temperature. Currently, the anodes of SOFCs are being studied in depth. Research has indicated that anodes based on a perovskite structure are a more promising candidate in SOFCs than the traditional system because they possess more favorable electrical properties. Among the perovskite-type oxides, SrTiO3 is one of the most promising compositions, with studies demonstrating that SrTiO3 exhibits particularly favorable electrical properties in contrast with other perovskite-type oxides. The main purpose of this article is to describe our study of the effect of rare-earth dopants with a perovskite structure on the electrical behavior of anodes in SOFCs. Sm2O3-doped SrTiO3 synthesized by a solid-state reaction was coated on substrate by atmospheric plasma spray. To compare the effect of the dopant on the electrical conductivity of strontium titanate, different concentrations of Sm2O3 were used. The samples were then investigated by x-ray diffraction, four-point probe at various temperatures (to determine the electrical conductivity), and a scanning electron microscope. The study showed that at room temperature, nondoped samples have a higher electrical resistance than doped samples. As the temperature was increased, the electrical

  14. Effect of Samarium Oxide on the Electrical Conductivity of Plasma-Sprayed SOFC Anodes

    Science.gov (United States)

    Panahi, S. N.; Samadi, H.; Nemati, A.

    2016-10-01

    Solid oxide fuel cells (SOFCs) are rapidly becoming recognized as a new alternative to traditional energy conversion systems because of their high energy efficiency. From an ecological perspective, this environmentally friendly technology, which produces clean energy, is likely to be implemented more frequently in the future. However, the current SOFC technology still cannot meet the demands of commercial applications due to temperature constraints and high cost. To develop a marketable SOFC, suppliers have tended to reduce the operating temperatures by a few hundred degrees. The overall trend for SOFC materials is to reduce their service temperature of electrolyte. Meanwhile, it is important that the other components perform at the same temperature. Currently, the anodes of SOFCs are being studied in depth. Research has indicated that anodes based on a perovskite structure are a more promising candidate in SOFCs than the traditional system because they possess more favorable electrical properties. Among the perovskite-type oxides, SrTiO3 is one of the most promising compositions, with studies demonstrating that SrTiO3 exhibits particularly favorable electrical properties in contrast with other perovskite-type oxides. The main purpose of this article is to describe our study of the effect of rare-earth dopants with a perovskite structure on the electrical behavior of anodes in SOFCs. Sm2O3-doped SrTiO3 synthesized by a solid-state reaction was coated on substrate by atmospheric plasma spray. To compare the effect of the dopant on the electrical conductivity of strontium titanate, different concentrations of Sm2O3 were used. The samples were then investigated by x-ray diffraction, four-point probe at various temperatures (to determine the electrical conductivity), and a scanning electron microscope. The study showed that at room temperature, nondoped samples have a higher electrical resistance than doped samples. As the temperature was increased, the electrical

  15. Realization of tin oxide like anode for the manufacture of the organic solar cells

    Directory of Open Access Journals (Sweden)

    Khelil A.

    2012-06-01

    Full Text Available The transparent oxides such as SnO2, In2O3 and ZnO continue to arouse a private interest for their various applications. The objective of the various studies being to carry out the layers which are simultaneously most transparent and most conducting possible. Thus in the field of the solar spectrum, the transmission of the layers must be higher than 80% and their conductivity exceeding 103 (Ohm.cm-1. Their transparency which is related to the value of their forbidden band must be higher than 3.7 e V. Their electric properties as for them depend on the composition of the layers and a possible doping. In this work, one characterized layers of SnO2 deposited by chemical pulverization, one carried out measurements by, electronic scan microscopy, diffraction of x-rays and also of the optical measurements and electronic. It results from it that the layers are conducting and transparent in the visible one but they are relatively rough, following its characterizations, one carried out organic photovoltaic cells using these layers of SnO2 and also of the commercial ITO like anode in these components. More particularly one was interested in the influence of the presence of a fine layer of gold between the anode and organic material.

  16. Electrochemical incineration of dimethyl phthalate by anodic oxidation with boron-doped diamond electrode

    Institute of Scientific and Technical Information of China (English)

    HOU Yining; QU Jiuhui; ZHAO Xu; LIU Huijuan

    2009-01-01

    The anodic oxidation of aqueous solutions containing dimethyl phthalate (DMP) up to 125 mg/L with sodium sulfate (Na2SO4) as supporting electrolyte within the pH range 2.0-10.0 was studied using a one-compartment batch reactor employing a boron-doped diamond (BDD) as anode. Electrolyses were carried out at constant current density (1.5-4.5 mA/cm2). Complete mineralization was always achieved owing to the great concentration of hydroxyl radical (·OH) generated at the BDD surface. The effect of pH, apparent current density and initial DMP concentration on the degradation rate of DMP, the specific charge required for its total mineralization and mineralization current efficiency was investigated systematically. The mineralization rate of DMP was found to be pH-independent and to increase with increasing applied current density. Results indicated that this electrochemical process was subjected, at least partially, to the mass transfer of organics onto the BDD surface. Kinetic analysis of the temporal change of DMP concentration during electrolysis determined by High Performance Liquid Chromatography (HPLC) revealed that DMP decay under all tested conditions followed a pseudo first-order reaction. Aromatic intermediates and generated carboxylic acids were identified by Gas Chromatography-Mass Spectrometry (GC-MS) and a general pathway for the electrochemical incineration of DMP on BDD was proposed.

  17. Oxygen effect of transparent conducting amorphous Indium Zinc Tin Oxide films on Polyimide substrate for flexible electrode

    International Nuclear Information System (INIS)

    This paper discusses the effect of oxygen on the transparent conducting properties and mechanical durability of the amorphous indium zinc tin oxide (IZTO) films. IZTO films deposited on flexible clear polyimide (PI) substrate using pulsed direct current (DC) magnetron sputtering at room temperature under various oxygen partial pressures. All IZTO films deposited at room temperature exhibit an amorphous structure. The electrical and optical properties of the IZTO films were sensitively influenced by oxygen partial pressures. At optimized deposition condition of 3.0% oxygen partial pressure, the IZTO film shows the lowest resistivity of 6.4 × 10−4 Ωcm, high transmittance of over 80% in the visible range, and figure of merit value of 3.6 × 10−3 Ω−1 without any heat controls. In addition, high work function and good mechanical flexibility of amorphous IZTO films are beneficial to flexible applications. It is proven that the proper oxygen partial pressure is important parameter to enhance the transparent conducting properties of IZTO films on PI substrate deposited at room temperature. - Highlights: • Indium zinc tin oxide (IZTO) films were deposited on polyimide at room temperature. • Transparent conducting properties of IZTO were influenced with oxygen partial pressure. • The smooth surface and high work function of IZTO were beneficial to anode layer. • The mechanical reliability of IZTO shows better performance to indium tin oxide film

  18. Electrochromism: from oxide thin films to devices

    Science.gov (United States)

    Rougier, A.; Danine, A.; Faure, C.; Buffière, S.

    2014-03-01

    In respect of their adaptability and performance, electrochromic devices, ECDs, which are able to change their optical properties under an applied voltage, have received significant attention. Target applications are multifold both in the visible region (automotive sunroofs, smart windows, ophthalmic lenses, and domestic appliances (oven, fridge…)) and in the infrared region (Satellites Thermal Control, IR furtivity). In our group, focusing on oxide thin films grown preferentially at room temperature, optimization of ECDs performances have been achieved by tuning the microstructure, the stoichiometry and the cationic composition of the various layers. Herein, our approach for optimized ECDs is illustrated through the example of WO3 electrochromic layer in the visible and in the IR domain as well as ZnO based transparent conducting oxide layer. Targeting the field of printed electronics, simplification of the device architecture for low power ECDs is also reported.

  19. Polyaniline-Coated Carbon Nanotube Ultrafiltration Membranes: Enhanced Anodic Stability for In Situ Cleaning and Electro-Oxidation Processes.

    Science.gov (United States)

    Duan, Wenyan; Ronen, Avner; Walker, Sharon; Jassby, David

    2016-08-31

    Electrically conducting membranes (ECMs) have been reported to be efficient in fouling prevention and destruction of aqueous chemical compounds. In the current study, highly conductive and anodically stable composite polyaniline-carbon nanotube (PANI-CNT) ultrafiltration (UF) ECMs were fabricated through a process of electropolymerization of aniline on a CNT substrate under acidic conditions. The resulting PANI-CNT UF ECMs were characterized by scanning electron microscopy, atomic force microscopy, a four-point conductivity probe, cyclic voltammetry, and contact angle goniometry. The utilization of the PANI-CNT material led to significant advantages, including: (1) increased electrical conductivity by nearly an order of magnitude; (2) increased surface hydrophilicity while not impacting membrane selectivity or permeability; and (3) greatly improved stability under anodic conditions. The membrane's anodic stability was evaluated in a pH-controlled aqueous environment under a wide range of anodic potentials using a three-electrode cell. Results indicate a significantly reduced degradation rate in comparison to a CNT-poly(vinyl alcohol) ECM under high anodic potentials. Fouling experiments conducted with bovine serum albumin demonstrated the capacity of the PANI-CNT ECMs for in situ oxidative cleaning, with membrane flux restored to its initial value under an applied potential of 3 V. Additionally, a model organic compound (methylene blue) was electrochemically transformed at high efficiency (90%) in a single pass through the anodically charged ECM. PMID:27525344

  20. Electrochromism of the electroless deposited cuprous oxide films

    International Nuclear Information System (INIS)

    Thin cuprous oxide films were prepared by a low cost, chemical deposition (electroless) method onto glass substrates pre-coated with fluorine doped tin oxide. The X-ray diffraction pattern confirmed the Cu2O composition of the films. Visible transmittance spectra of the cuprous oxide films were studied for the as-prepared, colored and bleached films. The cyclic voltammetry study showed that those films exhibited cathode coloring electrochromism, i.e. the films showed change of color from yellowish to black upon application of an electric field. The transmittance across the films for laser light of 670 nm was found to change due to the voltage change for about 50%. The coloration memory of those films was also studied during 6 h, ex-situ. The coloration efficiency at 670 nm was calculated to be 37 cm2/C

  1. Electrochromism of the electroless deposited cuprous oxide films

    Energy Technology Data Exchange (ETDEWEB)

    Neskovska, R. [Faculty of Technical Sciences, University ' St. Clement Ohridski' , Bitola (Macedonia, The Former Yugoslav Republic of); Ristova, M. [Faculty of Natural Sciences and Mathematics, Institute of Physics, P.O. Box 162, Skopje (Macedonia, The Former Yugoslav Republic of)]. E-mail: mristova@iunona.pmf.ukim.edu.mk; Velevska, J. [Faculty of Natural Sciences and Mathematics, Institute of Physics, P.O. Box 162, Skopje (Macedonia, The Former Yugoslav Republic of); Ristov, M. [Macedonian Academy of Sciences and Arts, Skopje, Bul. Krste Misirkov bb, Skopje (Macedonia, The Former Yugoslav Republic of)

    2007-04-09

    Thin cuprous oxide films were prepared by a low cost, chemical deposition (electroless) method onto glass substrates pre-coated with fluorine doped tin oxide. The X-ray diffraction pattern confirmed the Cu{sub 2}O composition of the films. Visible transmittance spectra of the cuprous oxide films were studied for the as-prepared, colored and bleached films. The cyclic voltammetry study showed that those films exhibited cathode coloring electrochromism, i.e. the films showed change of color from yellowish to black upon application of an electric field. The transmittance across the films for laser light of 670 nm was found to change due to the voltage change for about 50%. The coloration memory of those films was also studied during 6 h, ex-situ. The coloration efficiency at 670 nm was calculated to be 37 cm{sup 2}/C.

  2. Zinc oxide nanostructures by chemical vapour deposition as anodes for Li-ion batteries

    International Nuclear Information System (INIS)

    Highlights: • ZnO nanostructures are grown by simple chemical vapour deposition. • Polycrystalline nanostructured porous thin film is obtained. • Film exhibits stable specific capacity (∼400 mA h g−1) after prolonged cycling. • CVD-grown ZnO nanostructures show promising prospects as Li-ion battery anode. - Abstract: ZnO nanostructures are grown by a simple chemical vapour deposition method directly on a stainless steel disc current collector and successfully tested in lithium cells. The structural/morphological characterization points out the presence of well-defined polycrystalline nanostructures having different shapes and a preferential orientation along the c-axis direction. In addition, the high active surface of the ZnO nanostructures, which accounts for a large electrode/electrolyte contact area, and the complete wetting with the electrolyte solution are considered to be responsible for the good electrical transport properties and the adequate electrochemical behaviour, as confirmed by cyclic voltammetry and galvanostatic charge/discharge cycling. Indeed, despite no binder or conducting additives are used, when galvanostatically tested in lithium cells, after an initial decay, the ZnO nanostructures can provide a rather stable specific capacity approaching 70 μA h cm−2 (i.e., around 400 mA h g−1) after prolonged cycling at 1 C, with very high Coulombic efficiency and an overall capacity retention exceeding 62%

  3. Zinc oxide nanostructures by chemical vapour deposition as anodes for Li-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Laurenti, M., E-mail: marco.laurenti@iit.it [Center for Space Human Robotics @Polito, Istituto Italiano di Tecnologia, Corso Trento, 21, 10129 Turin (Italy); Department of Applied Science and Technology – DISAT, Politecnico di Torino, Corso Duca degli Abruzzi 24, 10129 Turin (Italy); Garino, N. [Center for Space Human Robotics @Polito, Istituto Italiano di Tecnologia, Corso Trento, 21, 10129 Turin (Italy); Porro, S.; Fontana, M. [Center for Space Human Robotics @Polito, Istituto Italiano di Tecnologia, Corso Trento, 21, 10129 Turin (Italy); Department of Applied Science and Technology – DISAT, Politecnico di Torino, Corso Duca degli Abruzzi 24, 10129 Turin (Italy); Gerbaldi, C., E-mail: claudio.gerbaldi@polito.it [Center for Space Human Robotics @Polito, Istituto Italiano di Tecnologia, Corso Trento, 21, 10129 Turin (Italy); Department of Applied Science and Technology – DISAT, Politecnico di Torino, Corso Duca degli Abruzzi 24, 10129 Turin (Italy)

    2015-08-15

    Highlights: • ZnO nanostructures are grown by simple chemical vapour deposition. • Polycrystalline nanostructured porous thin film is obtained. • Film exhibits stable specific capacity (∼400 mA h g{sup −1}) after prolonged cycling. • CVD-grown ZnO nanostructures show promising prospects as Li-ion battery anode. - Abstract: ZnO nanostructures are grown by a simple chemical vapour deposition method directly on a stainless steel disc current collector and successfully tested in lithium cells. The structural/morphological characterization points out the presence of well-defined polycrystalline nanostructures having different shapes and a preferential orientation along the c-axis direction. In addition, the high active surface of the ZnO nanostructures, which accounts for a large electrode/electrolyte contact area, and the complete wetting with the electrolyte solution are considered to be responsible for the good electrical transport properties and the adequate electrochemical behaviour, as confirmed by cyclic voltammetry and galvanostatic charge/discharge cycling. Indeed, despite no binder or conducting additives are used, when galvanostatically tested in lithium cells, after an initial decay, the ZnO nanostructures can provide a rather stable specific capacity approaching 70 μA h cm{sup −2} (i.e., around 400 mA h g{sup −1}) after prolonged cycling at 1 C, with very high Coulombic efficiency and an overall capacity retention exceeding 62%.

  4. Titania nanotubes from weak organic acid electrolyte: fabrication, characterization and oxide film properties.

    Science.gov (United States)

    Munirathinam, Balakrishnan; Neelakantan, Lakshman

    2015-04-01

    In this study, TiO2 nanotubes were fabricated using anodic oxidation in fluoride containing weak organic acid for different durations (0.5h, 1h, 2h and 3h). Scanning electron microscope (SEM) micrographs reveal that the morphology of titanium oxide varies with anodization time. Raman spectroscopy and X-ray diffraction (XRD) results indicate that the as-formed oxide nanotubes were amorphous in nature, yet transform into crystalline phases (anatase and rutile) upon annealing at 600°C. Wettability measurements show that both as-formed and annealed nanotubes exhibited hydrophilic behavior. The electrochemical behavior was ascertained by DC polarization and AC electrochemical impedance spectroscopy (EIS) measurements in 0.9% NaCl solution. The results suggest that the annealed nanotubes showed higher impedance (10(5)-10(6)Ωcm(2)) and lower passive current density (10(-7)Acm(-2)) than the as-formed nanotubes. In addition, we investigated the influence of post heat treatment on the semiconducting properties of the oxides by capacitance measurements. In vitro bioactivity test in simulated body fluid (SBF) showed that precipitation of Ca/P is easier in crystallized nanotubes than the amorphous structure. Our study uses a simple strategy to prepare nano-structured titania films and hints the feasibility of tailoring the oxide properties by thermal treatment, producing surfaces with better bioactivity. PMID:25686985

  5. Synthesis, characterization and performance of robust poison-resistant ultrathin film yttria stabilized zirconia - nickel anodes for application in solid electrolyte fuel cells

    Science.gov (United States)

    Garcia-Garcia, F. J.; Yubero, F.; Espinós, J. P.; González-Elipe, A. R.; Lambert, R. M.

    2016-08-01

    We report on the synthesis of undoped ∼5 μm YSZ-Ni porous thin films prepared by reactive pulsed DC magnetron sputtering at an oblique angle of incidence. Pre-calcination of the amorphous unmodified precursor layers followed by reduction produces a film consisting of uniformly distributed tilted columnar aggregates having extensive three-phase boundaries and favorable gas diffusion characteristics. Similarly prepared films doped with 1.2 at.% Au are also porous and contain highly dispersed gold present as Ni-Au alloy particles whose surfaces are strongly enriched with Au. With hydrogen as fuel, the performance of the undoped thin film anodes is comparable to that of 10-20 times thicker typical commercial anodes. With a 1:1 steam/carbon feed, the un-doped anode cell current rapidly falls to zero after 60 h. In striking contrast, the initial performance of the Au-doped anode is much higher and remains unaffected after 170 h. Under deliberately harsh conditions the performance of the Au-doped anodes decreases progressively, almost certainly due to carbon deposition. Even so, the cell maintains some activity after 3 days operation in dramatic contrast with the un-doped anode, which stops working after only three hours of use. The implications and possible practical application of these findings are discussed.

  6. Combining adsorption with anodic oxidation as an innovative technique for removal and destruction of organics.

    Science.gov (United States)

    Brown, N W; Roberts, E P L

    2013-01-01

    Coupling of adsorption with electrochemical oxidation is a novel approach to the treatment of aqueous organics that has demonstrated a number of key benefits over the individual application of these processes. This is based on a highly conducting adsorbent material, developed under the trade name Nyex™, that is able to rapidly adsorb the organics and anodically oxidise them within a single treatment unit. Successful scale up of the process (in both continuous and batch operation) has been achieved for the polishing of two separate groundwaters (one containing relatively simple petrol, diesel and their degradation products and the other with a range of more complex organics). Treatment showed that low discharge consents can be achieved, including the removal of more complex and difficult to treat compounds to below the limits of detection. Energy consumption for electrochemical regeneration was relatively low (down to 0.5 kWh/m(3)) suggesting that the process could be a practical alternative approach for effluent polishing.

  7. Synthesis of ordered Sinanowire arrays in porous anodic aluminum oxide templates

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    Highly ordered polycrystalline Si nanowire arrays were synthesized in porous anodic aluminum oxide (AAO) templates by the chemical vapor deposition (CVD)method. The morphological structure, the crystal character of Si nanowire arrays and the individual nanowire were analyzed by the transmission electron microscopy (TEM),scanning electron microscopy (SEM), atom force microscopy (AFM) and the X-ray diffraction spectrum (XRD), respectively. It is shown that most fabricated silicon nanowires (SiNWs) tend to be assembled parallelly in bundles and constructed with highly orientated arrays. This method provides a simple and low cost fabricating craftwork and the diameters and lengths of SiNWs can be controlled, the large area Si nanowire arrays can be achieved easily under such a way.The curling and twisting SiNWs are fewer than those by other synthesis methods.

  8. Solid oxide fuel cell anode image segmentation based on a novel quantum-inspired fuzzy clustering

    Science.gov (United States)

    Fu, Xiaowei; Xiang, Yuhan; Chen, Li; Xu, Xin; Li, Xi

    2015-12-01

    High quality microstructure modeling can optimize the design of fuel cells. For three-phase accurate identification of Solid Oxide Fuel Cell (SOFC) microstructure, this paper proposes a novel image segmentation method on YSZ/Ni anode Optical Microscopic (OM) images. According to Quantum Signal Processing (QSP), the proposed approach exploits a quantum-inspired adaptive fuzziness factor to adaptively estimate the energy function in the fuzzy system based on Markov Random Filed (MRF). Before defuzzification, a quantum-inspired probability distribution based on distance and gray correction is proposed, which can adaptively adjust the inaccurate probability estimation of uncertain points caused by noises and edge points. In this study, the proposed method improves accuracy and effectiveness of three-phase identification on the micro-investigation. It provides firm foundation to investigate the microstructural evolution and its related properties.

  9. Oxidation phase growth diagram of vanadium oxides film fabricated by rapid thermal annealing

    Institute of Scientific and Technical Information of China (English)

    Tamura KOZO; Zheng-cao LI; Yu-quan WANG; Jie NI; Yin HU; Zheng-jun ZHANG

    2009-01-01

    Thermal evaporation deposited vanadium oxide films were annealed in air by rapid thermal annealing (RTP). By adjusting the annealing temperature and time, a series of vanadium oxide films with various oxidation phases and surface morphologies were fabricated, and an oxidation phase growth diagram was established. It was observed that different oxidation phases appear at a limited and continuous annealing condition range, and the morphologic changes are related to the oxidation process.

  10. Dysprosium oxide and dysprosium-oxide-doped titanium oxide thin films grown by atomic layer deposition

    Energy Technology Data Exchange (ETDEWEB)

    Tamm, Aile, E-mail: aile.tamm@ut.ee; Kozlova, Jekaterina; Aarik, Lauri; Aarik, Jaan [Institute of Physics, University of Tartu, Ravila 14c, EE-50411 Tartu (Estonia); Kukli, Kaupo [University of Helsinki, FI-00014 Helsinki (Finland); Link, Joosep; Stern, Raivo [National Institute of Chemical Physics and Biophysics, Akadeemia tee 23, EE-12618 Tallinn (Estonia)

    2015-01-15

    Dysprosium oxide and dysprosium-oxide-doped titanium oxide thin films were grown by atomic layer deposition on silicon substrates. For depositing dysprosium and titanium oxides Dy(thd){sub 3}-O{sub 3} and TiCl{sub 4}-O{sub 3} were used as precursors combinations. Appropriate parameters for Dy(thd){sub 3}-O{sub 3} growth process were obtained by using a quartz crystal microbalance system. The Dy{sub 2}O{sub 3} films were deposited on planar substrates and on three-dimensional substrates with aspect ratio 1:20. The Dy/Ti ratio of Dy{sub 2}O{sub 3}-doped TiO{sub 2} films deposited on a planar silicon substrate ranged from 0.04 to 0.06. Magnetometry studies revealed that saturation of magnetization could not be observed in planar Dy{sub 2}O{sub 3} films, but it was observable in Dy{sub 2}O{sub 3} films on 3D substrates and in doped TiO{sub 2} films with a Dy/Ti atomic ratio of 0.06. The latter films exhibited saturation magnetization 10{sup −6} A cm{sup 2} and coercivity 11 kA/m at room temperature.

  11. Boron-doped diamond anodic oxidation of ethidium bromide: Process optimization by response surface methodology

    International Nuclear Information System (INIS)

    Highlights: ► Boron-doped diamond was used to degrade ethidium bromide. ► The process was optimized by a central composite rotatable design coupled with response surface methodology. ► Applied current is proved to be the most significant variable. ► A possible reaction sequence involving all the detected byproducts was proposed. - Abstract: The degradation of ethidium bromide (EtBr), a DNA intercalating pollutant, had been studied by anodic oxidation on boron-doped diamond (BDD) electrode under galvanostatic conditions. A central composite rotatable design coupled with response surface methodology was implemented to optimize the various operating parameters involved, among initial pH, flow rate, applied current and supporting electrolyte concentration, on the treatment efficiency; the latter was assessed in terms of color removal, COD removal, specific energy consumption and general current efficiency. Of the four parameters involved, applied current had a considerable effect on all the response factors. Optimum EtBr degradation was achieved by applying a current of 0.90 A, 9.0 mM Na2SO4, flow rate of 400 ml min−1 and pH 6.2 at 60 min of electrolysis, being reduced color by 80.2% and COD by 29.7%, with an energy consumption of 398.32 kW h (kg COD)−1 and a general current efficiency of 10.1%. Under these optimized conditions, EtBr decays followed pseudo first-order kinetics. Moreover, HPLC analysis of the BDD-treated solution allowed the detection of a number of reaction intermediates, and a possible reaction sequence involving all the detected byproducts was proposed for the electrochemical oxidation of EtBr on BDD anode.

  12. Anodic oxidation of coke oven wastewater: Multiparameter optimization for simultaneous removal of cyanide, COD and phenol.

    Science.gov (United States)

    Sasidharan Pillai, Indu M; Gupta, Ashok K

    2016-07-01

    Anodic oxidation of industrial wastewater from a coke oven plant having cyanide including thiocyanate (280 mg L(-1)), chemical oxygen demand (COD - 1520 mg L(-1)) and phenol (900 mg L(-1)) was carried out using a novel PbO2 anode. From univariate optimization study, low NaCl concentration, acidic pH, high current density and temperature were found beneficial for the oxidation. Multivariate optimization was performed with cyanide including thiocyanate, COD and phenol removal efficiencies as a function of changes in initial pH, NaCl concentration and current density using Box-Behnken experimental design. Optimization was performed for maximizing the removal efficiencies of these three parameters simultaneously. The optimum condition was obtained as initial pH 3.95, NaCl as 1 g L(-1) and current density of 6.7 mA cm(-2), for which the predicted removal efficiencies were 99.6%, 86.7% and 99.7% for cyanide including thiocyanate, COD and phenol respectively. It was in agreement with the values obtained experimentally as 99.1%, 85.2% and 99.7% respectively for these parameters. The optimum conditions with initial pH constrained to a range of 6-8 was initial pH 6, NaCl as 1.31 g L(-1) and current density as 6.7 mA cm(-2). The predicted removal efficiencies were 99%, 86.7% and 99.6% for the three parameters. The efficiencies obtained experimentally were in agreement at 99%, 87.8% and 99.6% respectively. The cost of operation for degradation at optimum conditions was calculated as 21.4 USD m(-3). PMID:27039363

  13. Surface characteristics of hydroxyapatite films deposited on anodized titanium by an electrochemical method

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Kang [Research Institute, Kuwotech, 970–88, Wolchul-dong, Buk-ku, Gwangju (Korea, Republic of); Department of Dental Materials and Research Center of Nano-Interface Activation for Biomaterials, School of Dentistry, Chosun University, Gwangju (Korea, Republic of); Jeong, Yong-Hoon; Brantley, William A. [Division of Restorative, Prosthetic and Primary Care Dentistry, College of Dentistry, The Ohio State, University, Columbus, OH (United States); Choe, Han-Cheol, E-mail: hcchoe@chosun.ac.kr [Department of Dental Materials and Research Center of Nano-Interface Activation for Biomaterials, School of Dentistry, Chosun University, Gwangju (Korea, Republic of)

    2013-11-01

    The biocompatibility of anodized titanium (Ti) was improved by an electrochemically deposited calcium phosphate (CaP) layer. The CaP layer was grown on the anodized Ti surface in modified simulated body fluid (M-SBF) at 85 °C. The phases and morphologies for the CaP layers were influenced by the electrolyte concentration. Nano flake-like precipitates that formed under low M-SBF concentrations were identified as hydroxyapatite (HAp) crystals orientated in the c-axis direction. In high M-SBF concentrations, the CaP layer formed micro plate-like precipitates on anodized Ti, and micropores were covered with HAp. Proliferation of murine preosteoblast cell (MC3T3-E1) on the HAp/anodized Ti surfaces was significantly higher than for untreated Ti and anodized Ti surfaces. - Highlights: • CaP layers were grown on anodized Ti surfaces by an electrochemical deposition process. • Phases and morphologies of layers were influenced by the electrolyte concentration. • Superior cell proliferation was observed on hydroxyapatite-coated anodized surfaces.

  14. Surface characteristics of hydroxyapatite films deposited on anodized titanium by an electrochemical method

    International Nuclear Information System (INIS)

    The biocompatibility of anodized titanium (Ti) was improved by an electrochemically deposited calcium phosphate (CaP) layer. The CaP layer was grown on the anodized Ti surface in modified simulated body fluid (M-SBF) at 85 °C. The phases and morphologies for the CaP layers were influenced by the electrolyte concentration. Nano flake-like precipitates that formed under low M-SBF concentrations were identified as hydroxyapatite (HAp) crystals orientated in the c-axis direction. In high M-SBF concentrations, the CaP layer formed micro plate-like precipitates on anodized Ti, and micropores were covered with HAp. Proliferation of murine preosteoblast cell (MC3T3-E1) on the HAp/anodized Ti surfaces was significantly higher than for untreated Ti and anodized Ti surfaces. - Highlights: • CaP layers were grown on anodized Ti surfaces by an electrochemical deposition process. • Phases and morphologies of layers were influenced by the electrolyte concentration. • Superior cell proliferation was observed on hydroxyapatite-coated anodized surfaces

  15. Electrocatalytic Oxidation of Cellulose to Gluconate on Carbon Aerogel Supported Gold Nanoparticles Anode in Alkaline Medium

    Directory of Open Access Journals (Sweden)

    Hanshuang Xiao

    2015-12-01

    Full Text Available The development of high efficient and low energy consumption approaches for the transformation of cellulose is of high significance for a sustainable production of high value-added feedstocks. Herein, electrocatalytic oxidation technique was employed for the selective conversion of cellulose to gluconate in alkaline medium by using concentrated HNO3 pretreated carbon aerogel (CA supported Au nanoparticles as anode. Results show that a high gluconate yield of 67.8% and sum salts yield of 88.9% can be obtained after 18 h of electrolysis. The high conversion of cellulose and high selectivity to gluconate could be attributed to the good dissolution of cellulose in NaOH solution which promotes its hydrolysis, the surface oxidized CA support and Au nanoparticles catalyst which possesses high amount of active sites. Moreover, the bubbled air also plays important role in the enhancement of cellulose electrocatalytic conversion efficiency. Lastly, a probable mechanism for electrocatalytic oxidation of cellulose to gluconate in alkaline medium was also proposed.

  16. Fabrication and formation of bioactive anodic zirconium oxide nanotubes containing presynthesized hydroxyapatite via alternative immersion method

    International Nuclear Information System (INIS)

    Hydroxyapatite (HA) coating has been widely applied on metallic biomedical implants to enhance their biocompatibility. It has been reported that HA coating can be formed on annealed zirconium with anodic zirconium oxide nanotubular arrays after immersion in simulated biological fluid (SBF) for about 14 days. In the present study, we apply an alternative immersion method (AIM) to form presynthesized HA on ZrO2 nanotubes. The AIM-treated specimen was then moved to the SBF to evaluate the capability for the formation of HA on it. The HA coating formed after only 2 days immersion and thickened after 5 days in the SBF. The HA coating is the carbonated HA with a ratio of Ca to P of about 1.4, similar to the physiological HA containing other minor elements such as Mg and Na. The results demonstrate that the AIM treatment is indeed suitable for the zirconium oxide nanotubes and highly accelerates the formation of HA coating in comparison with the existing methods, i.e. the annealing of the as-formed zirconium oxide nanotubular arrays.

  17. The role of subsurface oxygen in the local oxidation of zirconium and zirconium nitride thin films

    Energy Technology Data Exchange (ETDEWEB)

    Farkas, N.; Zhang, G.; Donnelly, K.M.; Evans, E.A.; Ramsier, R.D.; Dagata, J.A

    2004-01-30

    This paper discusses the growth kinetics of nanometer scale oxide structures grown by atomic force microscope (AFM) assisted lithography. The addition of nitrogen into the sputtering gas during zirconium deposition results in a crystalline ZrN material with oxygen held in solid solution. The diffusion rate of oxygen is high through the crystalline material, allowing it to participate in local anodization and resulting in tall oxide features at low relative humidity. These nanostructures are, in some cases, an order of magnitude higher than previously seen in other material systems. Higher nitrogen content in the plasma results in a crystalline to amorphous transition in the films, and the height enhancement of the AFM-grown features disappears. We propose that mass transport of subsurface oxygen has an influence on surface oxidation kinetics in this material system.

  18. Physics of thin films advances in research and development, v.6

    CERN Document Server

    Francombe, Maurice H

    1971-01-01

    Physics of Thin Films: Advances in Research and Development, Volume 6 reviews the rapid progress that has been made in research and development concerning the physics of thin films, with emphasis on metallic films. Topics covered include anodic oxide films, thin metal films and wires, and multilayer magnetic films. This volume is comprised of five chapters and begins with a discussion on the dielectric properties and the technique of plasma anodization which are relevant to the applications of anodic oxide films in electronic devices. Conduction, polarization, and dielectric breakdown effects

  19. Rational Design of Photonic Dust from Nanoporous Anodic Alumina Films: A Versatile Photonic Nanotool for Visual Sensing

    Science.gov (United States)

    Chen, Yuting; Santos, Abel; Wang, Ye; Kumeria, Tushar; Ho, Daena; Li, Junsheng; Wang, Changhai; Losic, Dusan

    2015-08-01

    Herein, we present a systematic study on the development, optimisation and applicability of interferometrically coloured distributed Bragg reflectors based on nanoporous anodic alumina (NAA-DBRs) in the form of films and nanoporous microparticles as visual/colorimetric analytical tools. Firstly, we synthesise a complete palette of NAA-DBRs by galvanostatic pulse anodisation approach, in which the current density is altered in a periodic fashion in order to engineer the effective medium of the resulting photonic films in depth. NAA-DBR photonic films feature vivid colours that can be tuned across the UV-visible-NIR spectrum by structural engineering. Secondly, the effective medium of the resulting photonic films is assessed systematically by visual analysis and reflectometric interference spectroscopy (RIfS) in order to establish the most optimal nanoporous platforms to develop visual/colorimetric tools. Then, we demonstrate the applicability of NAA-DBR photonic films as a chemically selective sensing platform for visual detection of mercury(II) ions. Finally, we generate a new nanomaterial, so-called photonic dust, by breaking down NAA-DBRs films into nanoporous microparticles. The resulting microparticles (μP-NAA-DBRs) display vivid colours and are sensitive towards changes in their effective medium, opening new opportunities for developing advanced photonic nanotools for a broad range of applications.

  20. Optical and vibrational spectra analysis of CVD - mixed oxide films: Optimization of the films electrochromic performance

    Energy Technology Data Exchange (ETDEWEB)

    Ivanova, T; Gesheva, K A [Central Laboratory of Solar Energy and New Energy Sources, Bulgarian Academy of Sciences, 72 Tzarigradsko Chaussee, 1784 Sofia (Bulgaria); Abrashev, M [Faculty of Physics, St. Kl. Ohridski University of Sofia, 5 J. Bourchier Blvd., 1164 Sofia (Bulgaria); Sharlandjiev, P; Nazarova, D, E-mail: kagesh@phys.bas.b [Central Laboratory of Optical Storage and Processing of Information, Bulgarian Academy of Sciences, Acad. G. Bonchev Str., Bl. 101, 1113 Sofia (Bulgaria)

    2010-04-01

    Mixed oxide films based on Mo and W were successfully prepared by atmospheric pressure CVD at the low substrate temperature of 200{sup o}C. High amount of oxygen was used to ensure a high degree of oxidation resulting in more stoichiometric oxide films. The structural transformations under different thermal treatments were studied by Raman spectroscopy and FTIR spectroscopy analysis. The films were characterized electrochemically by cyclic voltammetry using different electrolytes, scan rates, etc. The mixed oxide films exhibited a strong electrochromic (EC) effect.

  1. Optical and vibrational spectra analysis of CVD - mixed oxide films: Optimization of the films electrochromic performance

    International Nuclear Information System (INIS)

    Mixed oxide films based on Mo and W were successfully prepared by atmospheric pressure CVD at the low substrate temperature of 200oC. High amount of oxygen was used to ensure a high degree of oxidation resulting in more stoichiometric oxide films. The structural transformations under different thermal treatments were studied by Raman spectroscopy and FTIR spectroscopy analysis. The films were characterized electrochemically by cyclic voltammetry using different electrolytes, scan rates, etc. The mixed oxide films exhibited a strong electrochromic (EC) effect.

  2. Growth and Characterization of Epitaxial Oxide Thin Films

    OpenAIRE

    Garg, Ashish

    2001-01-01

    Epitaxial oxide thin films are used in many technologically important device applications. This work deals with the deposition and characterization of epitaxial WO3 and SrBi2Ta2O9 (SBT) thin films on single crystal oxide substrates. WO3 thin films were chosen as a subject of study because of recent findings of superconductivity at surfaces and twin boundaries in the bulk form of this oxide. Highly epitaxial thin films would be desirable in order to be able to create a device withi...

  3. Chitosan–silver oxide nanocomposite film: Preparation and antimicrobial activity

    Indian Academy of Sciences (India)

    Shipra Tripathi; G K Mehrotra; P K Dutta

    2011-02-01

    The chitosan–silver oxide encapsulated nanocomposite film was prepared by solution casting method. The prepared film was characterized by FTIR, scanning electron microscopy (SEM), thermal studies, and UV-Vis spectroscopy. The elemental composition of the film was studied by energy dispersive X-ray analysis (EDAX). The antibacterial activity of the composite film against pathogenic bacteria viz. Escherichia coli, Staphylococcus aureus, Bacillus subtilis and Pseudomonas aeruginosa was measured by agar diffusion method. Our observations suggest that chitosan as biomaterial based nanocomposite film containing silver oxide has an excellent antibacterial ability for food packaging applications.

  4. Highly Ordered Zinc Oxide Nanotubules Synthesized within the Anodic Aluminum Oxide Template

    Institute of Scientific and Technical Information of China (English)

    WANG Zhen; LI HuLin

    2001-01-01

    @@ Zinc oxide (ZnO) is a wide-band-gap semiconductor, which has a broad range of applications, e.g., in pigment, rubber additives, gas sensors, varistors and transducers1. It has recently been demonstrated that nanophase zinc oxide can be used in photocells of the Gatzel type2, which results in improved current generation efficiency. The properties of high aspect ratios and small sizes of zinc oxide nanotubules or nanowires are expected to improve the luminescence efficiency of the electro-optical devices and the sensitivity of the chemical sensors3.

  5. Highly Ordered Zinc Oxide Nanotubules Synthesized within the Anodic Aluminum Oxide Template

    Institute of Scientific and Technical Information of China (English)

    WANG; Zhen

    2001-01-01

    Zinc oxide (ZnO) is a wide-band-gap semiconductor, which has a broad range of applications, e.g., in pigment, rubber additives, gas sensors, varistors and transducers1. It has recently been demonstrated that nanophase zinc oxide can be used in photocells of the Gatzel type2, which results in improved current generation efficiency. The properties of high aspect ratios and small sizes of zinc oxide nanotubules or nanowires are expected to improve the luminescence efficiency of the electro-optical devices and the sensitivity of the chemical sensors3.  ……

  6. Determination of Soil Base—Soluble Se by Anodic Stripping Voltammetry with Aurum Thin—Film Electrode

    Institute of Scientific and Technical Information of China (English)

    YANGZENG; HEYING; 等

    1994-01-01

    Determination of soil Se by anodic stripping voltammetry(ASV) with aurum thin-film electrode(ATFE)overcomes the interference of gold peak with selenium peak,and thus has a higher sensitivity with the miniumum detectable concentration being 0.017μg/mL,the standard deviation of the measured results leww than 0.012μg/g,the coefficient of variation lwoer than 10% ,and the recovery rate between 86% to 103%.Besides the measurement conditions,the digestion of soil sample was also studied in detail.

  7. Modelo predictivo del espesor de la capa de óxido y microdureza en aluminio Al3003-B14 y Al6063-T6 anodizado usando análisis multifactorial Oxide film thickness and microhardness prediction model of Al3003-B14 and Al6063-T6 anodized aluminum using multifactorial analysis

    Directory of Open Access Journals (Sweden)

    Leonardo Eladio Vergara Guillén

    2011-08-01

    Full Text Available En esta investigación se modela a partir de los parámetros del proceso el espesor de la capa de óxido y la microdureza de los aluminios Al3003 y Al6063 anodizados. Para ello se realizaron estudios de la microdureza y espesor de capa de la superficie anodizada, utilizando técnicas de análisis multifactorial y diseño robusto. Se establecieron los siguientes niveles de los parámetros del proceso: temperatura [15 °C, 25 °C], tiempo [30 min; 60 min], concentración de electrolito [1,2 M; 2 M], densidad de corriente [1 Amp/dm²; 3 Amp/dm²], aluminio [Al3003,Al6063] y como variable de ruido, la deformación plástica [0%, 10%, 20%, 30%]. Se propuso un diseño fraccionado 2(7-2 mixto, con el cual se efectuó un total de 48 pruebas usando soluciones electrolíticas de ácido sulfúrico. La medición de microdureza se realizó con un indentador Vickers con carga de 400 g; el espesor de la capa de óxido se captó mediante microscopia electrónica. A los resultados se les realizó un análisis de varianza (ANOVA, para determinar los factores significativos y la robustez de los efectos. Se encontraron resultados de microdureza [HV] [85,74-308,87]; y espesor de óxido [µm] [12,82- 94,69]. Finalmente, se muestran los modelos de predicción de cada una de las respuestas en función de los factores significativos estas ecuaciones permitirán seleccionar la microdureza y espesor de la capa de óxido para cumplir los requerimientos de un producto particular mediante una selección apropiada de los parámetros del proceso.In this research, the thickness of the oxide layer and the microhardness of anodized aluminum Al3003 and Al6063 are modeled based on process parameters. To this end, studies of the microhardness and the thickness layer of the anodized surface were made, via techniques of multifactorial analysis and robust design. The following levels of the process parameters were established: temperature [15°C, 25°C], time [30min; 60min

  8. Anode gas recirculation for improving the performance and cost of a 5-kW solid oxide fuel cell system

    Science.gov (United States)

    Torii, Ryohei; Tachikawa, Yuya; Sasaki, Kazunari; Ito, Kohei

    2016-09-01

    Solid oxide fuel cells (SOFCs) have the potential to efficiently convert chemical energy into electricity and heat and are expected to be implemented in stationary combined heat and power (CHP) systems. This paper presents the heat balance analysis for a 5-kW medium-sized integrated SOFC system and the evaluation of the effect of anode gas recirculation on the system performance. The risk of carbon deposition on an SOFC anode due to anode gas recirculation is also assessed using the C-H-O diagram obtained from thermodynamic equilibrium calculations. These results suggest that a higher recirculation ratio increases net fuel utilization and improves the electrical efficiency of the SOFC system. Furthermore, cost simulation of the SOFC system and comparison with the cost of electricity supply by a power grid indicates that the capital cost is sufficiently low to popularize the SOFC system in terms of the total cost over one decade.

  9. A modified anode/electrolyte structure for a solid oxide electrochemical cell and a method for making said structure

    DEFF Research Database (Denmark)

    2013-01-01

    -stabilised zirconium oxide electrolyte and (c) a metallic and/or a ceramic electrocatalyst in the shape of interlayers incorporated in the interface between the anode and the electrolyte. This assembly is first sintered at a given temperature and then at a lower temperature in reducing gas mixtures. These heat...... steps (a) and (b), (d) applying a layer of the selected anode backbone onto the electrolyte with applied interlayers, (e) sintering the raw assembly and (f) infiltrating the electrocatalyst precursor into the sintered assembly and heat treating the assembly to incorporate additional electrocatalyst into...... treatments resulted in a distribution of the metallic and/or ceramic interlayers in the electrolyte/anode backbone junction taking place. The structure is prepared by (a) depositing a ceramic interlayer onto one side of the electrolyte, (b) optionally applying a metallic interlayer thereon, (c) repeating...

  10. Degradation behavior of anode-supported solid oxide fuel cell using LNF cathode as function of current load

    Energy Technology Data Exchange (ETDEWEB)

    Komatsu, Takeshi; Yoshida, Yoshiteru; Watanabe, Kimitaka; Chiba, Reiichi; Taguchi, Hiroaki; Orui, Himeko; Arai, Hajime [NTT Energy and Environment Systems Laboratories, Atsugi-shi, Kanagawa 243-0198 (Japan)

    2010-09-01

    We investigated the effect of current loading on the degradation behavior of an anode-supported solid oxide fuel cell (SOFC). The cell consisted of LaNi{sub 0.6}Fe{sub 0.4}O{sub 3} (LNF), alumina-doped scandia stabilized zirconia (SASZ), and a Ni-SASZ cermet as the cathode, electrolyte, and anode, respectively. The test was carried out at 1073 K with constant loads of 0.3, 1.0, 1.5, and 2.3 A cm{sup -2}. The degradation rate, defined by the voltage loss during a fixed period (about 1000 h), was faster at higher current densities. From an impedance analysis, the degradation depended mainly on increases in the cathodic resistance, while the anodic and ohmic resistances contributed very little. The cathode microstructures were observed using scanning electron microscopy (SEM) and transmission electron microscopy (TEM). (author)

  11. Three-Dimensional Crumpled Reduced Graphene Oxide/MoS2 Nanoflowers: A Stable Anode for Lithium-Ion Batteries.

    Science.gov (United States)

    Xiong, Fangyu; Cai, Zhengyang; Qu, Longbing; Zhang, Pengfei; Yuan, Zefang; Asare, Owusu Kwadwo; Xu, Wangwang; Lin, Chao; Mai, Liqiang

    2015-06-17

    Recently, layered transition-metal dichalcogenides (TMDs) have gained great attention for their analogous graphite structure and high theoretical capacity. However, it has suffered from rapid capacity fading. Herein, we present the crumpled reduced graphene oxide (RGO) decorated MoS2 nanoflowers on carbon fiber cloth. The three-dimensional framework of interconnected crumpled RGO and carbon fibers provides good electronic conductivity and facile strain release during electrochemical reaction, which is in favor of the cycling stability of MoS2. The crumpled RGO decorated MoS2 nanoflowers anode exhibits high specific capacity (1225 mAh/g) and excellent cycling performance (680 mAh/g after 250 cycles). Our results demonstrate that the three-dimensional crumpled RGO/MoS2 nanoflowers anode is one of the attractive anodes for lithium-ion batteries.

  12. Investigation of Metal Oxide/Carbon Nano Material as Anode for High Capacity Lithium-ion Cells

    Science.gov (United States)

    Wu, James Jianjun; Hong, Haiping

    2014-01-01

    NASA is developing high specific energy and high specific capacity lithium-ion battery (LIB) technology for future NASA missions. Current state-of-art LIBs have issues in terms of safety and thermal stability, and are reaching limits in specific energy capability based on the electrochemical materials selected. For example, the graphite anode has a limited capability to store Li since the theoretical capacity of graphite is 372 mAh/g. To achieve higher specific capacity and energy density, and to improve safety for current LIBs, alternative advanced anode, cathode, and electrolyte materials are pursued under the NASA Advanced Space Power System Project. In this study, the nanostructed metal oxide, such as Fe2O3 on carbon nanotubes (CNT) composite as an LIB anode has been investigated.

  13. Degradation mechanisms in solid oxide electrolysis anodes: Cr poisoning and cation interdiffusion

    International Nuclear Information System (INIS)

    High temperature steam electrolysis is one of the most efficient processes for hydrogen generation from water with no CO2 emissions using electricity and heat from nuclear or concentrated solar plants. Solid Oxide Electrolytic Cells (SOEC) are the proposed technology being researched and developed for this purpose. Over a long period of operation of the cells, various sources for degradation in the cells' electrochemical performance prevail, and hence the cell resistance increases and the process becomes inefficient. Our research is aimed at identifying the mechanisms for the loss in the electrochemical performance of the cell, particularly of the oxygen electrode, namely the anode. We are performing post-mortem analysis of the anode materials from SOEC stacks that were subject to demonstration tests over 2000 hours. We are focusing on two mechanisms of degradation: i) on the diffusion and reaction of chromium from the stainless steel interconnects onto the bond layer (cobaltite) and electrode (manganite) surface; ii) inter-diffusion of electrode and composite cations dissociating the anode composition. Chromium penetrates into the electrode microstructure through vapour-phase or solid state transport and reacts with the electrode material to form secondary and inactive phases which block the active sites. We have employed Raman Spectroscopy and identified the secondary phases, on the surface of the bong layer, that include mainly Cr2O3, LaCrO3, La2O3 and Co3O4, which have much lower conductivity than the original perovskite structure. We used scanning Auger Electron Nano-spectroscopy (AES) to study the local variations in the air electrode and the bond layer microchemistry and microstructure on a nano-to-micron scale. Chromium was clearly seen to be present in the cobaltite bond layer, and the chromium content was observed to monotonically decrease along the thickness of the bond layer. The manganite and manganite/zirconia composite electrode layers did not

  14. Novel Mg-Doped SrMoO3 Perovskites Designed as Anode Materials for Solid Oxide Fuel Cells

    Directory of Open Access Journals (Sweden)

    Vanessa Cascos

    2016-07-01

    Full Text Available SrMo1−xMxO3−δ (M = Fe and Cr, x = 0.1 and 0.2 oxides have been recently described as excellent anode materials for solid oxide fuel cells at intermediate temperatures (IT-SOFC with LSGM as the electrolyte. In this work, we have improved their properties by doping with aliovalent Mg ions at the B-site of the parent SrMoO3 perovskite. SrMo1−xMgxO3−δ (x = 0.1, 0.2 oxides have been prepared, characterized and tested as anode materials in single solid-oxide fuel cells, yielding output powers near 900 mW/cm−2 at 850 °C using pure H2 as fuel. We have studied its crystal structure with an “in situ” neutron power diffraction (NPD experiment at temperatures as high as 800 °C, emulating the working conditions of an SOFC. Adequately high oxygen deficiencies, observed by NPD, together with elevated disk-shaped anisotropic displacement factors suggest a high ionic conductivity at the working temperatures. Furthermore, thermal expansion measurements, chemical compatibility with the LSGM electrolyte, electronic conductivity and reversibility upon cycling in oxidizing-reducing atmospheres have been carried out to find out the correlation between the excellent performance as an anode and the structural features.

  15. Kinetics of the electrolytic Fe+2/Fe+3 oxidation on various anode materials

    Directory of Open Access Journals (Sweden)

    Cifuentes, L.

    2003-08-01

    Full Text Available The kinetics of the electrolytic Fe+2/Fe+3 oxidation, relevant to hydro-electrometallurgical processing, have been studied on lead, platinum, ruthenium oxide, iridium oxide and graphite anodes in ferrous sulfate-sulfuric acid solutions. The oxidation rate depends on ferrous sulfate concentration, solution temperature and degree of agitation. Potentiodynamic studies show that: a the highest oxidation rate is obtained on platinum; b lead is unsuitable as anodic material for the said reaction; c the remaining anode materials show a similar and satisfactory performance.

    Se ha estudiado la cinética de la oxidación electrolítica Fe+2/Fe+3 -relevante para el procesamiento hidroelectrometalúrgico- sobre plomo, platino, óxido de rutenio, óxido de iridio y grafito en soluciones de sulfato ferroso en ácido sulfúrico. La velocidad de oxidación depende de la concentración de sulfato ferroso, la temperatura de la solución y el grado de agitación. Estudios potenciodinámicos demuestran que: a las mayores velocidades de oxidación se obtienen sobre platino; b el plomo es inadecuado como material anódico para la reacción mencionada; c los materiales anódicos restantes exhiben un desempeño similar y satisfactorio.

  16. Chemical Liquid Phase Deposition of Thin Aluminum Oxide Films

    OpenAIRE

    Sun, Jie; Sun, Yingchun

    2007-01-01

    Thin aluminum oxide films were deposited by a new and simple physicochemical method called chemical liquid phase deposition (CLD) on semiconductor materials. Aluminum sulfate with crystallized water and sodium bicarbonate were used as precursors for film growth, and the control of the system pH value played an important role in this experiment. The growth rate is 12 nm/h at room temperature. Post-growth annealing not only densifies and purifies the films, but results in film crystallization a...

  17. Mild oxidation treatment of graphite anode for Li-ion batteries

    Institute of Scientific and Technical Information of China (English)

    GUO Hua-jun; LI Xin-hai; WANG Zhi-xing; PENG Wen-jie; GUO Yong-xing

    2005-01-01

    The graphite was modified by mild oxidation, and the effects of modification temperature and soaking time on the characteristics of graphite were investigated. The structure and characteristics of the graphite were determined by X-ray diffraction, scanning electron microscopy, BET surface area, particle size analysis and electrochemical measurements. The results show that the modified graphite has a better-developed crystallite structure, larger average particle diameter, smaller surface area, and better electrochemical characteristics than the untrented graphite. The sample mild-oxidized at 600 ℃ for 3 h has the best electrochemical performances with a reversible capacity of 304.5 mA·h/g, a irreversible capacity of 66.4 mA·h/g, and a initial coulombic efficiency of 82.1%. The charge/discharge properties and a cycling stability of the prototype lithium ion batteries with modified graphite as anodes are improved. Its capacity retention ratio at the 200th cycle is enhanced from 66.75% to 90.15%.

  18. The effect of H2S on the performance of Ni-YSZ anodes in solid oxide fuel cells

    DEFF Research Database (Denmark)

    Rasmussen, Jens Foldager Bregnballe; Hagen, Anke

    2009-01-01

    Biomass-derived fuel, e.g. biogas, is a potential fuel for solid oxide fuel cells (SOFCs). At operating temperature (850 °C) reforming of the carbon-containing biogas takes place over the Ni-containing anode. However, impurities in the biogas, e.g. H2S, can poison both the reforming...... and the electrochemical activity of the anode. Tests of single anode-supported planar SOFCs were carried out in the presence of H2S under current load at 850 °C. The cell voltage dropped as we periodically added 2–100 ppm H2S to an H2-containing fuel in 24 h intervals, but it regenerated to the initial value after we...... turned off the H2S. Evaluation of the changes of the cell voltage suggests that saturation coverage was reached at approximately 40 ppm H2S. A front-like movement of S-poisoning over the anode was seen by monitoring the in-plane voltage in the anode. Furthermore, impedance spectra showed that mainly...

  19. Electrochemical, structural and surface characterization of nickel/zirconia solid oxide fuel cell anodes in coal gas containing antimony

    Science.gov (United States)

    Marina, Olga A.; Pederson, Larry R.; Coyle, Christopher A.; Thomsen, Edwin C.; Nachimuthu, Ponnusamy; Edwards, Danny J.

    The interactions of antimony with the nickel-zirconia anode in solid oxide fuel cells (SOFCs) have been investigated. Tests with both anode-supported and electrolyte-supported button cells were performed at 700 and 800 °C in synthetic coal gas containing 100 ppb to 9 ppm antimony. Minor performance loss was observed immediately after Sb introduction to coal gas resulting in ca. 5% power output drop. While no further degradation was observed during the following several hundred hours of testing, cells abruptly and irreversibly failed after 800-1600 h depending on Sb concentration and test temperature. Antimony was found to interact strongly with nickel resulting in extensive alteration phase formation, consistent with expectations based on thermodynamic properties. Nickel antimonide phases, NiSb and Ni 5Sb 2, were partially coalesced into large grains and eventually affected electronic percolation through the anode support. Initial degradation was attributed to diffusion of antimony to the active anode/electrolyte interface to form an adsorption layer, while the late stage degradation was due the Ni-Sb phase formation. Assuming an average Sb concentration in coal gas of 0.07 ppmv, a 500 μm thick Ni/zirconia anode-supported cell is not expected to fail within 7 years when operated at a power output of 0.5 W cm -2 and fuel utilization above 50%.

  20. Synthesis of zinc oxide porous structures by anodization with water as an electrolyte

    Energy Technology Data Exchange (ETDEWEB)

    Shetty, Amitha; Nanda, Karuna Kar [Indian Institute of Science, Materials Research Centre, Bangalore (India)

    2012-10-15

    We report a simple, reliable and one-step method of synthesizing ZnO porous structures at room temperature by anodization of zinc (Zn) sheet with water as an electrolyte and graphite as a counter electrode. We observed that the de-ionized (DI) water used in the experiment is slightly acidic (pH=5.8), which is due to the dissolution of carbon dioxide from the atmosphere forming carbonic acid. Porous ZnO is characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), Raman spectroscopy and photoluminescence (PL) studies. The current-transient measurement is carried out using a Gamry Instruments Reference 3000 and the thickness of the deposited films is measured using a Dektak surface profilometer. The PL, Raman and X-ray photoelectron spectroscopy are used to confirm the presence of ZnO phase. We have demonstrated that the hybrid structures of ZnO and poly (3,4-ethylenedioxythiophene):poly (styrene sulfonate) (PEDOT:PSS) exhibit good rectifying characteristics. The evaluated barrier height and the ideality factor are 0.45 eV and 3.6, respectively. (orig.)