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Sample records for porous anodic oxide

  1. Morphological instability leading to formation of porous anodic oxide films

    NASA Astrophysics Data System (ADS)

    Hebert, Kurt R.; Albu, Sergiu P.; Paramasivam, Indhumati; Schmuki, Patrik

    2012-02-01

    Electrochemical oxidation of metals, in solutions where the oxide is somewhat soluble, produces anodic oxides with highly regular arrangements of pores. Although porous aluminium and titanium oxides have found extensive use in functional nanostructures, pore initiation and self-ordering are not yet understood. Here we present an analysis that examines the roles of oxide dissolution and ionic conduction in the morphological stability of anodic films. We show that patterns of pores with a minimum spacing are possible only within a narrow range of the oxide formation efficiency (the fraction of oxidized metal atoms retained in the film), which should exist when the metal ion charge exceeds two. Experimentally measured efficiencies, over diverse anodizing conditions on both aluminium and titanium, lie within the different ranges predicted for each metal. On the basis of these results, the relationship between dissolution chemistry and the conditions for pore initiation can now be understood in quantitative terms.

  2. Morphological instability leading to formation of porous anodic oxide films.

    PubMed

    Hebert, Kurt R; Albu, Sergiu P; Paramasivam, Indhumati; Schmuki, Patrik

    2012-02-01

    Electrochemical oxidation of metals, in solutions where the oxide is somewhat soluble, produces anodic oxides with highly regular arrangements of pores. Although porous aluminium and titanium oxides have found extensive use in functional nanostructures, pore initiation and self-ordering are not yet understood. Here we present an analysis that examines the roles of oxide dissolution and ionic conduction in the morphological stability of anodic films. We show that patterns of pores with a minimum spacing are possible only within a narrow range of the oxide formation efficiency (the fraction of oxidized metal atoms retained in the film), which should exist when the metal ion charge exceeds two. Experimentally measured efficiencies, over diverse anodizing conditions on both aluminium and titanium, lie within the different ranges predicted for each metal. On the basis of these results, the relationship between dissolution chemistry and the conditions for pore initiation can now be understood in quantitative terms. PMID:22138790

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

    NASA Astrophysics Data System (ADS)

    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.

  4. A Highly Controllable Electrochemical Anodization Process to Fabricate Porous Anodic Aluminum Oxide Membranes

    NASA Astrophysics Data System (ADS)

    Lin, Yuanjing; Lin, Qingfeng; Liu, Xue; Gao, Yuan; He, Jin; Wang, Wenli; Fan, Zhiyong

    2015-12-01

    Due to the broad applications of porous alumina nanostructures, research on fabrication of anodized aluminum oxide (AAO) with nanoporous structure has triggered enormous attention. While fabrication of highly ordered nanoporous AAO with tunable geometric features has been widely reported, it is known that its growth rate can be easily affected by the fluctuation of process conditions such as acid concentration and temperature during electrochemical anodization process. To fabricate AAO with various geometric parameters, particularly, to realize precise control over pore depth for scientific research and commercial applications, a controllable fabrication process is essential. In this work, we revealed a linear correlation between the integrated electric charge flow throughout the circuit in the stable anodization process and the growth thickness of AAO membranes. With this understanding, we developed a facile approach to precisely control the growth process of the membranes. It was found that this approach is applicable in a large voltage range, and it may be extended to anodization of other metal materials such as Ti as well.

  5. A Highly Controllable Electrochemical Anodization Process to Fabricate Porous Anodic Aluminum Oxide Membranes.

    PubMed

    Lin, Yuanjing; Lin, Qingfeng; Liu, Xue; Gao, Yuan; He, Jin; Wang, Wenli; Fan, Zhiyong

    2015-12-01

    Due to the broad applications of porous alumina nanostructures, research on fabrication of anodized aluminum oxide (AAO) with nanoporous structure has triggered enormous attention. While fabrication of highly ordered nanoporous AAO with tunable geometric features has been widely reported, it is known that its growth rate can be easily affected by the fluctuation of process conditions such as acid concentration and temperature during electrochemical anodization process. To fabricate AAO with various geometric parameters, particularly, to realize precise control over pore depth for scientific research and commercial applications, a controllable fabrication process is essential. In this work, we revealed a linear correlation between the integrated electric charge flow throughout the circuit in the stable anodization process and the growth thickness of AAO membranes. With this understanding, we developed a facile approach to precisely control the growth process of the membranes. It was found that this approach is applicable in a large voltage range, and it may be extended to anodization of other metal materials such as Ti as well. PMID:26706687

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

    NASA Astrophysics Data System (ADS)

    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.

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

    NASA Astrophysics Data System (ADS)

    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.

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

    NASA Astrophysics Data System (ADS)

    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.

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

    NASA Astrophysics Data System (ADS)

    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.

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

    SciTech Connect

    Xiao, Anguo 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.

  11. Model of porous aluminium oxide growth during initial stage of anodization

    NASA Astrophysics Data System (ADS)

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

    2014-10-01

    Currently, the development of nanotechnology and metamaterials requires the ability to obtain regular self-assembled structures with different parameters. One such structure is porous alumina in which the pores grow perpendicular to the substrate and are hexagonally packed. Pore size and the distance between them can be varied depending on the anodization voltage, the electrolyte and the anodization time (pore diameter - from 2 to 350 nm, the distance between the pores - from 5 to 50 nm). At the moment, there are different models describing the process of anodizing aluminum, in this paper we propose a model that takes into account the effect of layers of aluminum, aluminum oxide, and the electrolyte, as well as the influence of the effect of surface diffusion.

  12. Electrodeposition of cerium oxide on porous silicon via anodization and enhancement of photoluminescence

    NASA Astrophysics Data System (ADS)

    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.

  13. Design of capillary flows with functionally graded porous titanium oxide films fabricated by anodization instability.

    PubMed

    Joung, Young Soo; Figliuzzi, Bruno Michel; Buie, Cullen R

    2014-06-01

    We have developed an electrochemical fabrication method utilizing breakdown anodization (BDA) to yield capillary flows that can be expressed as functions of capillary height. This method uses anodization instability with high electric potentials and mildly acidic electrolytes that are maintained at low temperature. BDA produces highly porous micro- and nano-structured surfaces composed of amorphous titanium oxide on titanium substrates, resulting in high capillary pressure and capillary diffusivity. With this fabrication technique the capillary flow properties can be controlled by varying the applied electric field and electrolyte temperature. Furthermore, they can be expressed as functions of capillary height when customized electric fields are used in BDA. To predict capillary flows on BDA surfaces, we developed a conceptual model of highly wettable porous films, which are modeled as multiple layers of capillary tubes oriented in the flow direction. From the model, we derived a general capillary flow equation of motion in terms of capillary pressure and capillary diffusivity, both of which can be expressed as functions of capillary height. The theoretical model was verified by comparisons with experimental capillary flows, showing good agreement. From investigation of the surface morphology we found that the surface structures were also functionally graded with respect to the capillary height (i.e. applied electric field). The suggested fabrication method and the theoretical model offer novel design methodologies for microscale liquid transport devices requiring control over propagation speed. PMID:24703679

  14. The role of stress in self-ordered porous anodic oxide formation and corrosion of aluminum

    NASA Astrophysics Data System (ADS)

    Capraz, Omer Ozgur

    The phenomenon of plastic flow induced by electrochemical reactions near room temperature is significant in porous anodic oxide (PAO) films, charging of lithium batteries and stress-corrosion cracking (SCC). As this phenomenon is poorly understood, fundamental insight into flow from our work may provide useful information for these problems. In-situ monitoring of the stress state allows direct correlation between stress and the current or potential, thus providing fundamental insight into technologically important deformation and failure mechanisms induced by electrochemical reactions. A phase-shifting curvature interferometry was designed to investigate the stress generation mechanisms on different systems. Resolution of our curvature interferometry was found to be ten times more powerful than that obtained by state-of-art multiple deflectometry technique and the curvature interferometry helps to resolve the conflicting reports in the literature. During this work, formation of surface patterns during both aqueous corrosion of aluminum and formation of PAO films were investigated. Interestingly, for both cases, stress induced plastic flow controls the formation of surface patterns. Pore formation mechanisms during anodizing of the porous aluminum oxide films was investigated . PAO films are formed by the electrochemical oxidation of metals such as aluminum and titanium in a solution where oxide is moderately soluble. They have been used extensively to design numerous devices for optical, catalytic, and biological and energy related applications, due to their vertically aligned-geometry, high-specific surface area and tunable geometry by adjusting process variables. These structures have developed empirically, in the absence of understanding the process mechanism. Previous experimental studies of anodizing-induced stress have extensively focused on the measurement of average stress, however the measurement of stress evolution during anodizing does not provide

  15. Optical properties of one-dimensional photonic crystals based on porous films of anodic aluminum oxide

    NASA Astrophysics Data System (ADS)

    Gorelik, V. S.; Klimonsky, S. O.; Filatov, V. V.; Napolskii, K. S.

    2016-04-01

    The optical properties of one-dimensional photonic crystals based on porous anodic aluminum oxide films have been studied by measuring transmittance and specular reflectance spectra in the visible and UV spectral regions. Angular dependences of the spectral positions of optical stop bands are obtained. It is shown that the reflectance within the first stop band varies from point to point on the sample surface, reaching a level of 98-99% at some points. The dispersion relation for electromagnetic waves in the model of infinite periodic structure is calculated for the samples under study. The possibility of using models with an infinite or finite number of layers to calculate reflectance spectra near the first optical stop band is discussed.

  16. Short time proton dynamics in bulk ice and in porous anode solid oxide fuel cell materials

    SciTech Connect

    Basoli, Francesco; Senesi, Roberto; Kolesnikov, Alexander I; Licoccia, Silvia

    2014-01-01

    Oxygen reduction and incorporation into solid electrolytes and the reverse reaction of oxygen evolution play a cru-cial role in Solid Oxide Fuel Cell (SOFC) applications. However a detailed un derstanding of the kinetics of the cor-responding reactions, i.e. on reaction mechanisms, rate limiting steps, reaction paths, electrocatalytic role of materials, is still missing. These include a thorough characterization of the binding potentials experienced by protons in the lattice. We report results of Inelastic Neutron Scattering (INS) measurements of the vibrational state of the protons in Ni- YSZ highly porous composites (75% to 90% ), a ceramic-metal material showing a high electrical conductivity and ther mal stability, which is known to be most effectively used as anodes for solid ox ide fuel cells. The results are compared with INS and Deep Inelastic Neutron Scattering (DINS) experiments on the proton binding states in bulk ice.

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

    SciTech Connect

    Chai, Y.; Yam, F. K.; Hassan, Z.

    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.

  18. 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

    NASA Astrophysics Data System (ADS)

    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.

  19. Fabrication of super slippery sheet-layered and porous anodic aluminium oxide surfaces and its anticorrosion property

    NASA Astrophysics Data System (ADS)

    Song, Tingting; Liu, Qi; Liu, Jingyuan; Yang, Wanlu; Chen, Rongrong; Jing, Xiaoyan; Takahashi, Kazunobu; Wang, Jun

    2015-11-01

    Inspired by natural plants such as Nepenthes pitcher plants, super slippery surfaces have been developed to improve the attributes of repellent surfaces. In this report, super slippery porous anodic aluminium oxide (AAO) surfaces have fabricated by a simple and reproducible method. Firstly, the aluminium substrates were treated by an anodic process producing micro-nano structured sheet-layered pores, and then immersed in Methyl Silicone Oil, Fluororalkylsilane (FAS) and DuPont Krytox, respectively, generating super slippery surfaces. Such a good material with excellent anti-corrosion property through a simple and repeatable method may be potential candidates for metallic application in anti-corrosion and extreme environment.

  20. Study and characterization of porous copper oxide produced by electrochemical anodization for radiometric heat absorber

    PubMed Central

    2014-01-01

    The aim of this work is to optimize the different parameters for realization of an absorbing cavity to measure the incident absolute laser energy. Electrochemical oxidation is the background process that allowed the copper blackening. A study of the blackened surface quality was undertaken using atomic force microscopy (AFM) analysis and ultraviolet-visible-infrared spectrophotometry using a Shimadzu spectrophotometer. A two-dimensional and three-dimensional visualization by AFM of the formed oxide coating showed that the copper surfaces became porous after electrochemical etching with different roughness. This aspect is becoming more and more important with decreasing current density anodization. In a 2 mol L -1 of NaOH solution, at a temperature of 90°C, and using a 16 mA cm2 constant density current, the copper oxide formed has a reflectivity of around 3% in the spectral range between 300 and 1,800 nm. Using the ‘mirage effect’ technique, the obtained Cu2O diffusivity and thermal conductivity are respectively equal to (11.5 ± 0.5) 10 to 7 m2 s-1 and (370 ± 20) Wm-1 K-1. This allows us to consider that our Cu2O coating is a good thermal conductor. The results of the optical and thermal studies dictate the choice of the cavity design. The absorbing cavity is a hollow cylinder machined to its base at an angle of 30°. If the included angle of the plane is 30° and the interior surface gives specular reflection, an incoming ray parallel to the axis will undergo five reflections before exit. So the absorption of the surface becomes closely near 0.999999. PMID:25349555

  1. Study and characterization of porous copper oxide produced by electrochemical anodization for radiometric heat absorber.

    PubMed

    Ben Salem, Sonia; Achour, Zahra Ben; Thamri, Kamel; Touayar, Oualid

    2014-01-01

    The aim of this work is to optimize the different parameters for realization of an absorbing cavity to measure the incident absolute laser energy. Electrochemical oxidation is the background process that allowed the copper blackening. A study of the blackened surface quality was undertaken using atomic force microscopy (AFM) analysis and ultraviolet-visible-infrared spectrophotometry using a Shimadzu spectrophotometer. A two-dimensional and three-dimensional visualization by AFM of the formed oxide coating showed that the copper surfaces became porous after electrochemical etching with different roughness. This aspect is becoming more and more important with decreasing current density anodization. In a 2 mol L(-1) of NaOH solution, at a temperature of 90°C, and using a 16 mA cm(2) constant density current, the copper oxide formed has a reflectivity of around 3% in the spectral range between 300 and 1,800 nm. Using the 'mirage effect' technique, the obtained Cu2O diffusivity and thermal conductivity are respectively equal to (11.5 ± 0.5) 10 to 7 m(2) s(-1) and (370 ± 20) Wm(-1) K(-1). This allows us to consider that our Cu2O coating is a good thermal conductor. The results of the optical and thermal studies dictate the choice of the cavity design. The absorbing cavity is a hollow cylinder machined to its base at an angle of 30°. If the included angle of the plane is 30° and the interior surface gives specular reflection, an incoming ray parallel to the axis will undergo five reflections before exit. So the absorption of the surface becomes closely near 0.999999. PMID:25349555

  2. Study and characterization of porous copper oxide produced by electrochemical anodization for radiometric heat absorber

    NASA Astrophysics Data System (ADS)

    Ben Salem, Sonia; Achour, Zahra Ben; Thamri, Kamel; Touayar, Oualid

    2014-10-01

    The aim of this work is to optimize the different parameters for realization of an absorbing cavity to measure the incident absolute laser energy. Electrochemical oxidation is the background process that allowed the copper blackening. A study of the blackened surface quality was undertaken using atomic force microscopy (AFM) analysis and ultraviolet-visible-infrared spectrophotometry using a Shimadzu spectrophotometer. A two-dimensional and three-dimensional visualization by AFM of the formed oxide coating showed that the copper surfaces became porous after electrochemical etching with different roughness. This aspect is becoming more and more important with decreasing current density anodization. In a 2 mol L -1 of NaOH solution, at a temperature of 90°C, and using a 16 mA cm2 constant density current, the copper oxide formed has a reflectivity of around 3% in the spectral range between 300 and 1,800 nm. Using the `mirage effect' technique, the obtained Cu2O diffusivity and thermal conductivity are respectively equal to (11.5 ± 0.5) 10 to 7 m2 s-1 and (370 ± 20) Wm-1 K-1. This allows us to consider that our Cu2O coating is a good thermal conductor. The results of the optical and thermal studies dictate the choice of the cavity design. The absorbing cavity is a hollow cylinder machined to its base at an angle of 30°. If the included angle of the plane is 30° and the interior surface gives specular reflection, an incoming ray parallel to the axis will undergo five reflections before exit. So the absorption of the surface becomes closely near 0.999999.

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

    PubMed

    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

  4. Syntheses of rare-earth metal oxide nanotubes by the sol-gel method assisted with porous anodic aluminum oxide templates

    SciTech Connect

    Kuang Qin; Lin Zhiwei; Lian Wei; Jiang Zhiyuan; Xie Zhaoxiong Huang Rongbin; Zheng Lansun

    2007-04-15

    In this paper, we report a versatile synthetic method of ordered rare-earth metal (RE) oxide nanotubes. RE (RE=Y, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Yb) oxide nanotubes were successfully prepared from corresponding RE nitrate solution via the sol-gel method assisted with porous anodic aluminum oxide (AAO) templates. Scanning electron microscopy (SEM), transmission electron microscopy (TEM), high-resolution TEM, and X-ray diffraction (XRD) have been employed to characterize the morphology and composition of the as-prepared nanotubes. It is found that as-prepared RE oxides evolve into bamboo-like nanotubes and entirely hollow nanotubes. A new possible formation mechanism of RE oxide nanotubes in the AAO channels is proposed. These high-quantity RE oxide nanotubes are expected to have promising applications in many areas such as luminescent materials, catalysts, magnets, etc. - Graphical abstract: A versatile synthetic method for the preparation of ordered rare-earth (RE) oxide nanotubes is reported, by which RE (RE=Y, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Yb) oxide nanotubes were successfully prepared from corresponding RE nitrate solution via the sol-gel method assisted with porous anodic aluminum oxide (AAO) templates.

  5. Modelling the initial stage of porous alumina growth during anodization

    NASA Astrophysics Data System (ADS)

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

    2013-05-01

    Artificially on the surface of aluminum there may be build a thick layer of Al2O3, which has a porous structure. In this paper we present a model of growth of porous alumina in the initial stage of anodizing, identifying dependencies anodizing parameters on the rate of growth of the film and the distance between the pores and as a result of the created model equations were found for changes in the disturbance of alumina for the initial stage of anodizing aluminum oxide porous border aluminum-alumina and alumina-electrolyte, with the influence of surface diffusion of aluminum oxide.

  6. Fabrication of Pd Micro-Membrane Supported on Nano-Porous Anodized Aluminum Oxide for Hydrogen Separation.

    PubMed

    Kim, Taegyu

    2015-08-01

    In the present study, nano-porous anodized aluminum oxide (AAO) was used as a support of the Pd membrane. The AAO fabrication process consists of an electrochemical polishing, first/second anodizing, barrier layer dissolving and pores widening. The Pd membrane was deposited on the AAO support using an electroless plating with ethylenediaminetetraacetic acid (EDTA) as a plating agent. The AAO had the regular pore structure with the maximum pore diameter of ~100 nm so it had a large opening area but a small free standing area. The 2 µm-thick Pd layer was obtained by the electroless plating for 3 hours. The Pd layer thickness increased with increasing the plating time. However, the thickness was limited to ~5 µm in maximum. The H2 permeation flux was 0.454 mol/m2-s when the pressure difference of 66.36 kPa0.5 was applied at the Pd membrane under 400 °C. PMID:26369167

  7. Fabrication of SERS-active substrates using silver nanofilm-coated porous anodic aluminum oxide for detection of antibiotics.

    PubMed

    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. PMID:25736080

  8. Influence of wet etching time cycles on morphology features of thin porous Anodic Aluminum oxide (AAO) template for nanostructure's synthesis

    NASA Astrophysics Data System (ADS)

    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. Metallizing porous scaffolds as an alternative fabrication method for solid oxide fuel cell anodes

    NASA Astrophysics Data System (ADS)

    Ruiz-Trejo, Enrique; Atkinson, Alan; Brandon, Nigel P.

    2015-04-01

    A combination of electroless and electrolytic techniques is used to incorporate nickel into a porous Ce0.9Gd0.1O1.90 scaffold. First a porous backbone was screen printed into a YSZ electrolyte using an ink that contains sacrificial pore formers. Once sintered, the scaffold was coated with silver using Tollens' reaction followed by electrodeposition of nickel in a Watts bath. At high temperatures the silver forms droplets enabling direct contact between the gadolinia-doped ceria and nickel. Using impedance spectroscopy analysis in a symmetrical cell a total area specific resistance of 1 Ωcm2 at 700 °C in 97% H2 with 3% H2O was found, indicating the potential of this fabrication method for scaling up.

  10. Doped, porous iron oxide films and their optical functions and anodic photocurrents for solar water splitting

    SciTech Connect

    Kronawitter, Coleman X.; Mao, Samuel S.; Antoun, Bonnie R.

    2011-02-28

    The fabrication and morphological, optical, and photoelectrochemical characterization of doped iron oxide films is presented. The complex index of refraction and absorption coefficient of polycrystalline films are determined through measurement and modeling of spectral transmission and reflection data using appropriate dispersion relations. Photoelectrochemical characterization for water photo-oxidation reveals that the conversion efficiencies of electrodes are strongly influenced by substrate temperature during their oblique-angle physical vapor deposition. These results are discussed in terms of the films' morphological features and the known optoelectronic limitations of iron oxide films for application in solar water splitting devices.

  11. ZIRCONIUM OXIDE NANOSTRUCTURES PREPARED BY ANODIC OXIDATION

    SciTech Connect

    Dang, Y. Y.; Bhuiyan, M.S.; Paranthaman, M. P.

    2008-01-01

    Zirconium oxide is an advanced ceramic material highly useful for structural and electrical applications because of its high strength, fracture toughness, chemical and thermal stability, and biocompatibility. If highly-ordered porous zirconium oxide membranes can be successfully formed, this will expand its real-world applications, such as further enhancing solid-oxide fuel cell technology. Recent studies have achieved various morphologies of porous zirconium oxide via anodization, but they have yet to create a porous layer where nanoholes are formed in a highly ordered array. In this study, electrochemical methods were used for zirconium oxide synthesis due to its advantages over other coating techniques, and because the thickness and morphology of the ceramic fi lms can be easily tuned by the electrochemical parameters, such as electrolyte solutions and processing conditions, such as pH, voltage, and duration. The effects of additional steps such as pre-annealing and post-annealing were also examined. Results demonstrate the formation of anodic porous zirconium oxide with diverse morphologies, such as sponge-like layers, porous arrays with nanoholes ranging from 40 to 75 nm, and nanotube layers. X-ray powder diffraction analysis indicates a cubic crystallographic structure in the zirconium oxide. It was noted that increased voltage improved the ability of the membrane to stay adhered to the zirconium substrate, whereas lower voltages caused a propensity for the oxide fi lm to fl ake off. Further studies are needed to defi ne the parameters windows that create these morphologies and to investigate other important characteristics such as ionic conductivity.

  12. Zirconium Oxide Nanostructures Prepared by Anodic Oxidation

    SciTech Connect

    Dang, Ying Yi; Bhuiyan, Md S; Paranthaman, Mariappan Parans

    2008-01-01

    Zirconium oxide is an advanced ceramic material highly useful for structural and electrical applications because of its high strength, fracture toughness, chemical and thermal stability, and biocompatibility. If highly-ordered porous zirconium oxide membranes can be successfully formed, this will expand its real-world applications, such as further enhancing solid-oxide fuel cell technology. Recent studies have achieved various morphologies of porous zirconium oxide via anodization, but they have yet to create a porous layer where nanoholes are formed in a highly ordered array. In this study, electrochemical methods were used for zirconium oxide synthesis due to its advantages over other coating techniques, and because the thickness and morphology of the ceramic films can be easily tuned by the electrochemical parameters, such as electrolyte solutions and processing conditions, such as pH, voltage, and duration. The effects of additional steps such as pre-annealing and post-annealing were also examined. Results demonstrate the formation of anodic porous zirconium oxide with diverse morphologies, such as sponge-like layers, porous arrays with nanoholes ranging from 40 to 75 nm, and nanotube layers. X-ray powder diffraction analysis indicates a cubic crystallographic structure in the zirconium oxide. It was noted that increased voltage improved the ability of the membrane to stay adhered to the zirconium substrate, whereas lower voltages caused a propensity for the oxide film to flake off. Further studies are needed to define the parameters windows that create these morphologies and to investigate other important characteristics such as ionic conductivity.

  13. Growth behavior of anodic porous alumina formed in malic acid solution

    NASA Astrophysics Data System (ADS)

    Kikuchi, Tatsuya; Yamamoto, Tsuyoshi; Suzuki, Ryosuke O.

    2013-11-01

    The growth behavior of anodic porous alumina formed on aluminum by anodizing in malic acid solutions was investigated. High-purity aluminum plates were electropolished in CH3COOH/HClO4 solutions and then anodized in 0.5 M malic acid solutions at 293 K and constant cell voltages of 200-350 V. The anodic porous alumina grew on the aluminum substrate at voltages of 200-250 V, and a black, burned oxide film was formed at higher voltages. The nanopores of the anodic oxide were only formed at grain boundaries of the aluminum substrate during the initial stage of anodizing, and then the growth region extended to the entire aluminum surface as the anodizing time increased. The anodic porous alumina with several defects was formed by anodizing in malic acid solution at 250 V, and oxide cells were approximately 300-800 nm in diameter.

  14. Analysis of possibilities for carbon removal from porous anode of solid oxide fuel cells after different failure modes

    NASA Astrophysics Data System (ADS)

    Subotić, Vanja; Schluckner, Christoph; Schroettner, Hartmuth; Hochenauer, Christoph

    2016-01-01

    This study focuses on the investigation of possibilities for carbon removal from the fuel electrode of anode supported solid oxide fuel cells (ASC-SOFCs) after different degradation modes. To design the conditions which generally lead the cell in the range of carbon depositions the performed thermodynamic calculations show that the SOFC operating temperature range seems to be appropriate for formation of elemental carbon in various types. Concerning this the loaded large planar single SOFCs are fed with synthetic diesel reformate thus simulating realistic operating conditions and enabling the formation and deposition of carbon on the anode side. A mixture of hydrogen/water vapor/nitrogen is used to remove the detected carbon depositions in a cell-protecting manner. For the purpose of this investigation several failure modes are induced after which determination the already defined regeneration strategy is applied. The cathode degradation is first induced and secondly the fuel supply is interrupted to induce re-oxidation of nickel (Ni) on the anode side. The undertaken investigations determine that carbon can be fully removed from the anode surface after nickel oxidation, while cathode degradation disables the complete cell regeneration.

  15. Electrophoretic deposition of multi-walled carbon nanotubes on porous anodic aluminum oxide using ionic liquid as a dispersing agent

    NASA Astrophysics Data System (ADS)

    Hekmat, F.; Sohrabi, B.; Rahmanifar, M. S.; Jalali, A.

    2015-06-01

    Multi-wall carbon nanotubes (MW-CNTs) have been arranged in nanochannels of anodic aluminum oxide template (AAO) by electrophoretic deposition (EPD) to make a vertically-aligned carbon nanotube (VA-CNT) based electrode. Well ordered AAO templates were prepared by a two-step anodizing process by applying a constant voltage of 45 V in oxalic acid solution. The stabilized CNTs in a water-soluble room temperature ionic liquid (1-methyl-3-octadecylimidazolium bromide), were deposited in the pores of AAO templates which were conductive by deposition of Ni nanoparticles in the bottom of pores. In order to obtain ideal results, different EPD parameters, such as concentration of MWCNTs and ionic liquid on stability of MWCNT suspensions, deposition time and voltage which are applied in EPD process and also optimal conditions for anodizing of template were investigated. The capacitive performance of prepared electrodes was analyzed by measuring the specific capacitance from cyclic voltammograms and the charge-discharge curves. A maximum value of 50 Fg-1 at the scan rate of 20 mV s-1was achieved for the specific capacitance.

  16. Chemical synthesis, characterisation, and biocompatibility of nanometre scale porous anodic aluminium oxide membranes for use as a cell culture substrate for the vero cell line: a preliminary study.

    PubMed

    Poinern, Gérrard Eddy Jai; Le, Xuan Thi; O'Dea, Mark; Becker, Thomas; Fawcett, Derek

    2014-01-01

    In this preliminary study we investigate for the first time the biomedical potential of using porous anodic aluminium oxide (AAO) membranes as a cell substrate for culturing the Cercopithecus aethiops (African green monkey) Kidney (Vero) epithelial cell line. One advantage of using the inorganic AAO membrane is the presence of nanometre scale pore channels that allow the exchange of molecules and nutrients across the membrane. The size of the pore channels can be preselected by adjusting the controlling parameters of a temperature controlled two-step anodization process. The cellular interaction and response of the Vero cell line with an in-house synthesised AAO membrane, a commercially available membrane, and a glass control were assessed by investigating cell adhesion, morphology, and proliferation over a 72 h period. The number of viable cells proliferating over the respective membrane surfaces revealed that the locally produced in-house AAO membrane had cells numbers similar to the glass control. The study revealed evidence of focal adhesion sites over the surface of the nanoporous membranes and the penetration of cellular extensions into the pore structure as well. The outcome of the study has revealed that nanometre scale porous AAO membranes have the potential to become practical cell culture scaffold substrates with the capability to enhance adhesion and proliferation of Vero cells. PMID:24579077

  17. Chemical Synthesis, Characterisation, and Biocompatibility of Nanometre Scale Porous Anodic Aluminium Oxide Membranes for Use as a Cell Culture Substrate for the Vero Cell Line: A Preliminary Study

    PubMed Central

    Poinern, Gérrard Eddy Jai; Le, Xuan Thi; Becker, Thomas; Fawcett, Derek

    2014-01-01

    In this preliminary study we investigate for the first time the biomedical potential of using porous anodic aluminium oxide (AAO) membranes as a cell substrate for culturing the Cercopithecus aethiops (African green monkey) Kidney (Vero) epithelial cell line. One advantage of using the inorganic AAO membrane is the presence of nanometre scale pore channels that allow the exchange of molecules and nutrients across the membrane. The size of the pore channels can be preselected by adjusting the controlling parameters of a temperature controlled two-step anodization process. The cellular interaction and response of the Vero cell line with an in-house synthesised AAO membrane, a commercially available membrane, and a glass control were assessed by investigating cell adhesion, morphology, and proliferation over a 72 h period. The number of viable cells proliferating over the respective membrane surfaces revealed that the locally produced in-house AAO membrane had cells numbers similar to the glass control. The study revealed evidence of focal adhesion sites over the surface of the nanoporous membranes and the penetration of cellular extensions into the pore structure as well. The outcome of the study has revealed that nanometre scale porous AAO membranes have the potential to become practical cell culture scaffold substrates with the capability to enhance adhesion and proliferation of Vero cells. PMID:24579077

  18. Impedance spectroscopy of highly ordered nano-porous electrodes based on Au-AAO (anodic aluminum oxide) structure.

    PubMed

    Ahn, Jaehwan; Cho, Sungbo; Min, Junhong

    2013-11-01

    Electrochemical measurements using the microelectrodes are increasingly utilized for the label-free detection of the small amount of biological materials such as DNA, protein, and cells. However, the interfacial electrode impedance increases and may hinder the detection of weak signals as the size of electrode decreases. To enhance the measurement sensitivity while reducing the electrode size, in this study, microelectrodes employing a nanoporous structure were fabricated and characterized by using electrical impedance spectroscopy. We made the highly ordered honeycomb nanoporous structure of Anodic Aluminum Oxide (AAO) by electrochemical anodizing and formed Au layer on the surface of AAO (Au/AAO) by electroless Au plating method. The electrical characteristics of the fabricated Au/AAO electrodes were evaluated by using de Levie's model derived for the pore electrodes. As a result, the interfacial electrode impedance of the fabricated Au/AAO electrodes was 2-3 order lower than the value of the planar electrodes at frequencies below 1 kHz. It implies this nanoporous electrode could be directly applied to label free detection of biomaterials. PMID:24245278

  19. Lithium intercalation in porous carbon anodes

    SciTech Connect

    Tran, T.D.; Pekala, R.W.; Mayer, S.T.

    1994-11-23

    Carbon foams derived from the phase separation of polyacrylonitrile/solvent mixtures were investigated as lithium intercalation anodes for rechargeable lithium-ion batteries. The carbon foams have a bulk density of 0.35--0.5 g/cm{sup 3}, low surface area (< 50 m{sup 2}/g), and an average cell size of 5--10 {mu}m. Polyacrylonitrile-based carbon foams doped with phosphoric acid had capacity as high as 450 mAh/g. Carbon capacity increased with increasing phosphoric acid concentration in the doping solution. The doped porous carbon anodes exhibited good cyclability and excellent coulombic efficiency.

  20. Growth behavior of anodic oxide formed by aluminum anodizing in glutaric and its derivative acid electrolytes

    NASA Astrophysics Data System (ADS)

    Nakajima, Daiki; Kikuchi, Tatsuya; Natsui, Shungo; Suzuki, Ryosuke O.

    2014-12-01

    The growth behavior of anodic oxide films formed via anodizing in glutaric and its derivative acid solutions was investigated based on the acid dissociation constants of electrolytes. High-purity aluminum foils were anodized in glutaric, ketoglutaric, and acetonedicarboxylic acid solutions under various electrochemical conditions. A thin barrier anodic oxide film grew uniformly on the aluminum substrate by glutaric acid anodizing, and further anodizing caused the film to breakdown due to a high electric field. In contrast, an anodic porous alumina film with a submicrometer-scale cell diameter was successfully formed by ketoglutaric acid anodizing at 293 K. However, the increase and decrease in the temperature of the ketoglutaric acid resulted in non-uniform oxide growth and localized pitting corrosion of the aluminum substrate. An anodic porous alumina film could also be fabricated by acetonedicarboxylic acid anodizing due to the relatively low dissociation constants associated with the acid. Acid dissociation constants are an important factor for the fabrication of anodic porous alumina films.

  1. Fabrication of porous anodic alumina using normal anodization and pulse anodization

    NASA Astrophysics Data System (ADS)

    Chin, I. K.; Yam, F. K.; Hassan, Z.

    2015-05-01

    This article reports on the fabrication of porous anodic alumina (PAA) by two-step anodizing the low purity commercial aluminum sheets at room temperature. Different variations of the second-step anodization were conducted: normal anodization (NA) with direct current potential difference; pulse anodization (PA) alternate between potential differences of 10 V and 0 V; hybrid pulse anodization (HPA) alternate between potential differences of 10 V and -2 V. The method influenced the film homogeneity of the PAA and the most homogeneous structure was obtained via PA. The morphological properties are further elucidated using measured current-transient profiles. The absent of current rise profile in PA indicates the anodization temperature and dissolution of the PAA structure were greatly reduced by alternating potential differences.

  2. Anodic oxidation of benzoquinone using diamond anode.

    PubMed

    Panizza, Marco

    2014-01-01

    The anodic degradation of 1,4-benzoquinone (BQ), one of the most toxic xenobiotic, was investigated by electrochemical oxidation at boron-doped diamond anode. The electrolyses have been performed in a single-compartment flow cell in galvanostatic conditions. The influence of applied current (0.5-2 A), BQ concentration (1-2 g dm(-3)), temperature (20-45 °C) and flow rate (100-300 dm(3) h(-1)) has been studied. BQ decay kinetic, the evolution of its oxidation intermediates and the mineralization of the aqueous solutions were monitored during the electrolysis by high-performance liquid chromatograph (HPLC) and chemical oxygen demand (COD) measurements. The results obtained show that the use of diamond anode leads to total mineralization of BQ in any experimental conditions due to the production of oxidant hydroxyl radicals electrogenerated from water discharge. The decay kinetics of BQ removal follows a pseudo-first-order reaction, and the rate constant increases with rising current density. The COD removal rate was favoured by increasing of applied current, recirculating flow rate and it is almost unaffected by solution temperature. PMID:24710725

  3. Synthesis of aluminum oxy-hydroxide nanofibers from porous anodic alumina.

    PubMed

    Jha, Himendra; Kikuchi, Tatsuya; Sakairi, Masatoshi; Takahashi, Hideaki

    2008-10-01

    A novel method for the synthesis of aluminum oxy-hydroxide nanofibers from a porous anodic oxide film of aluminum is demonstrated. In the present method, the porous anodic alumina not only acts as a template, but also serves as the starting material for the synthesis. The porous anodic alumina film is hydrothermally treated for pore-sealing, which forms aluminum oxy-hydroxide inside the pores of the oxide film as well as on the surface of the film. The hydrothermally sealed porous oxide film is immersed in the sodium citrate solution, which selectively etches the porous aluminum oxide from the film, leaving the oxy-hydroxide intact. The method is simple and gives highly uniform aluminum oxy-hydroxide nanofibers. Moreover, the diameter of the nanofibers can be controlled by controlling the pore size of the porous anodic alumina film, which depends on the anodizing conditions. Nanofibers with diameters of about 38-85 nm, having uniform shape and size, were successfully synthesized using the present method. PMID:21832599

  4. Novel structure formation at the bottom surface of porous anodic alumina fabricated by single step anodization process.

    PubMed

    Ali, Ghafar; Ahmad, Maqsood; Akhter, Javed Iqbal; Maqbool, Muhammad; Cho, Sung Oh

    2010-08-01

    A simple approach for the growth of long-range highly ordered nanoporous anodic alumina film in H(2)SO(4) electrolyte through a single step anodization without any additional pre-anodizing procedure is reported. Free-standing porous anodic alumina film of 180 microm thickness with through hole morphology was obtained. A simple and single step process was used for the detachment of alumina from aluminum substrate. The effect of anodizing conditions, such as anodizing voltage and time on the pore diameter and pore ordering is discussed. The metal/oxide and oxide/electrolyte interfaces were examined by high resolution scanning transmission electron microscope. The arrangement of pores on metal/oxide interface was well ordered with smaller diameters than that of the oxide/electrolyte interface. The inter-pore distance was larger in metal/oxide interface as compared to the oxide/electrolyte interface. The size of the ordered domain was found to depend strongly upon anodizing voltage and time. PMID:20493719

  5. Controlling the anodizing conditions in preparation of an nanoporous anodic aluminium oxide template

    NASA Astrophysics Data System (ADS)

    Nazemi, Azadeh; Abolfazl, Seyed; Sadjadi, Seyed

    2014-12-01

    Porous anodic aluminium oxide (AAO) template is commonly used in the synthesis of one-dimensional nanostructures, such as nanowires and nanorods, due to its simple fabrication process. Controlling the anodizing conditions is important because of their direct influence on the size of AAO template pores; it affects the size of nanostructures that are fabricated in AAO template. In present study, several alumina templates were fabricated by a two-step electrochemical anodization in different conditions, such as the time of first process, its voltage, and electrolyte concentration. The effect of these factors on pore diameters of AAO templates was investigated using scanning electron microscopy (SEM).

  6. Impurity-defect structure of anodic aluminum oxide produced by two-sided anodizing in tartaric acid

    NASA Astrophysics Data System (ADS)

    Chernyakova, K. V.; Vrublevsky, I. A.; Ivanovskaya, M. I.; Kotsikau, D. A.

    2012-03-01

    Porous aluminum oxide is prepared in a 0.4 M aqueous solution of tartaric acid by two-sided anodizing. Fourier Transform IR spectroscopy (FTIR) data reveal the presence, in the alumina, of unoxidized tartarate ions, as well as products of their partial (radical organic products and CO) and complete (CO2) oxidation. Carboxylate ions and elemental carbon contained in the anodic oxide impart a gray color to the films.

  7. Photoluminescence structure, and composition of laterally anodized porous Si

    NASA Technical Reports Server (NTRS)

    Jung, K. H.; Shih, S.; Kwong, D. L.; George, T.; Lin, T. L.; Liu, H. Y.; Zavada, J.

    1992-01-01

    We have studied the photoluminescence (PL), structure, and composition of laterally anodized porous Si. Broad PL peaks were observed centered between about 620-720 nm with strong intensities measured from 500 to 860 nm. Macroscopic variations in PL intensities and peak positions are explained in terms of the structure and anodization process. Structural studies suggest that the PL appears to originate from a multilayered porous Si structure in which the top two layers are amorphous. X-ray diffraction spectra also suggest the presence of a significant amorphous phase. In addition to high concentrations of B and N, we have measured extremely high concentrations much greater than 10 exp 20 cu cm of H, C, O, and F. Our results indicate that laterally anodized porous Si does not fit the crystalline Si quantum wire model prevalent in the literature suggesting that some other structure is responsible for the observed luminescence.

  8. Ultrafast excited state deactivation of doped porous anodic alumina membranes

    NASA Astrophysics Data System (ADS)

    Makhal, Abhinandan; Sarkar, Soumik; Pal, Samir Kumar; Yan, Hongdan; Wulferding, Dirk; Cetin, Fatih; Lemmens, Peter

    2012-08-01

    Free-standing, bi-directionally permeable and ultra-thin anodic aluminum oxide (AAO) membranes establish attractive templates (host) for the synthesis of nano-dots and rods of various materials (guest). This is due to their chemical and structural integrity and high periodicity on length scales of 5-150 nm which are often used to host photoactive nano-materials for various device applications including dye-sensitized solar cells. In the present study, AAO membranes are synthesized by using electrochemical methods and a detailed structural characterization using FEG-SEM, XRD and TGA confirms the porosity and purity of the material. Defect-mediated photoluminescence quenching of the porous AAO membrane in the presence of an electron accepting guest organic molecule (benzoquinone) is studied by means of steady-state and picosecond/femtosecond-resolved luminescence measurements. Using time-resolved luminescence transients, we have also revealed light harvesting of complexes of porous alumina impregnated with inorganic quantum dots (Maple Red) or gold nanowires. Both the Förster resonance energy transfer and the nano-surface energy transfer techniques are employed to examine the observed quenching behavior as a function of the characteristic donor-acceptor distances. The experimental results will find their relevance in light harvesting devices based on AAOs combined with other materials involving a decisive energy/charge transfer dynamics.

  9. Porous aluminum room temperature anodizing process in a fluorinated-oxalic acid solution

    NASA Astrophysics Data System (ADS)

    Dhahri, S.; Fazio, E.; Barreca, F.; Neri, F.; Ezzaouia, H.

    2016-08-01

    Anodizing of aluminum is used for producing porous insulating films suitable for different applications in electronics and microelectronics. Porous-type aluminum films are most simply realized by galvanostatic anodizing in aqueous acidic solutions. The improvement in application of anodizing technique is associated with a substantial reduction of the anodizing voltage at appropriate current densities as well as to the possibility to carry out the synthesis process at room temperature in order to obtain a self-planarizing dielectric material incorporated in array of super-narrow metal lines. In this work, the anodizing of aluminum to obtain porous oxide was carried out, at room temperature, on three different substrates (glass, stainless steel and aluminum), using an oxalic acid-based electrolyte with the addition of a relatively low amount of 0.4 % of HF. Different surface morphologies, from nearly spherical to larger porous nanostructures with smooth edges, were observed by means of scanning electron microscopy. These evidences are explained by considering the formation, transport and adsorption of the fluorine species which react with the Al3+ ions. The behavior is also influenced by the nature of the original substrate.

  10. Formation of anodic aluminum oxide with serrated nanochannels.

    PubMed

    Li, Dongdong; Zhao, Liang; Jiang, Chuanhai; Lu, Jia G

    2010-08-11

    We report a simple and robust method to self-assemble porous anodic aluminum oxide membranes with serrated nanochannels by anodizing in phosphoric acid solution. Due to high field conduction and anionic incorporation, an increase of anodizing voltage leads to an increase of the impurity levels and also the field strength across barrier layer. On the basis of both experiment and simulation results, the initiation and formation of serrated channels are attributed to the evolution of oxygen gas bubbles followed by plastic deformation in the oxide film. Alternating anodization in oxalic and phosphoric acids is applied to construct multilayered membranes with smooth and serrated channels, demonstrating a unique way to design and construct a three-dimensional hierarchical system with controllable morphology and composition. PMID:20617804

  11. Inward Lithium-Ion Breathing of Hierarchically Porous Silicon Anodes

    DOE PAGESBeta

    Xiao, Qiangfeng; Gu, Meng; Yang, Hui; Li, Bing; Zhang, Cunman; Liu, Yang; Liu, Fang; Dai, Fang; Yang, Li; Liu, Zhongyi; et al

    2015-11-05

    Silicon has been identified as one of the most promising candidates as anode for high performance lithium-ion batteries. The key challenge for Si anodes is the large volume change induced chemomechanical fracture and subsequent rapid capacity fading upon cyclic charge and discharge. Improving capacity retention thus critically relies on smart accommodation of the volume changes through nanoscale structural design. In this work, we report a novel fabrication method for hierarchically porous Si nanospheres (hp-SiNSs), which consist of a porous shell and a hollow core. Upon charge/discharge cycling, the hp-SiNSs accommodate the volume change through reversible inward expansion/contraction with negligible particle-levelmore » outward expansion. Our mechanics analysis revealed that such a unique volume-change accommodation mechanism is enabled by the much stiffer modulus of the lithiated layer than the unlithiated porous layer and the low flow stress of the porous structure. Such inward expansion shields the hp-SiNSs from fracture, opposite to the outward expansion in solid Si during lithiation. Lithium ion battery assembled with this new nanoporous material exhibits high capacity, high power, long cycle life and high coulombic efficiency, which is superior to the current commercial Si-based anode materials. We find the low cost synthesis approach reported here provides a new avenue for the rational design of hierarchically porous structures with unique materials properties.« less

  12. Inward Lithium-Ion Breathing of Hierarchically Porous Silicon Anodes

    SciTech Connect

    Xiao, Qiangfeng; Gu, Meng; Yang, Hui; Li, Bing; Zhang, Cunman; Liu, Yang; Liu, Fang; Dai, Fang; Yang, Li; Liu, Zhongyi; Xiao, Xingcheng; Liu, Gao; Zhao, Peng; Zhang, Sulin; Wang, Chong M.; Lu, Yunfeng; Cai, Mei

    2015-11-05

    Silicon has been identified as one of the most promising candidates as anode for high performance lithium-ion batteries. The key challenge for Si anodes is the large volume change induced chemomechanical fracture and subsequent rapid capacity fading upon cyclic charge and discharge. Improving capacity retention thus critically relies on smart accommodation of the volume changes through nanoscale structural design. In this work, we report a novel fabrication method for hierarchically porous Si nanospheres (hp-SiNSs), which consist of a porous shell and a hollow core. Upon charge/discharge cycling, the hp-SiNSs accommodate the volume change through reversible inward expansion/contraction with negligible particle-level outward expansion. Our mechanics analysis revealed that such a unique volume-change accommodation mechanism is enabled by the much stiffer modulus of the lithiated layer than the unlithiated porous layer and the low flow stress of the porous structure. Such inward expansion shields the hp-SiNSs from fracture, opposite to the outward expansion in solid Si during lithiation. Lithium ion battery assembled with this new nanoporous material exhibits high capacity, high power, long cycle life and high coulombic efficiency, which is superior to the current commercial Si-based anode materials. The low cost synthesis approach reported here provides a new avenue for the rational design of hierarchically porous structures with unique materials properties.

  13. Inward Lithium-Ion Breathing of Hierarchically Porous Silicon Anodes

    SciTech Connect

    Xiao, Qiangfeng; Gu, Meng; Yang, Hui; Li, Bing; Zhang, Cunman; Liu, Yang; Liu, Fang; Dai, Fang; Yang, Li; Liu, Zhongyi; Xiao, Xingcheng; Liu, Gao; Zhao, Peng; Zhang, Sulin; Wang, Chong M.; Lu, Yunfeng; Cai, Mei

    2015-11-05

    Silicon has been identified as one of the most promising candidates as anode for high performance lithium-ion batteries. The key challenge for Si anodes is the large volume change induced chemomechanical fracture and subsequent rapid capacity fading upon cyclic charge and discharge. Improving capacity retention thus critically relies on smart accommodation of the volume changes through nanoscale structural design. In this work, we report a novel fabrication method for hierarchically porous Si nanospheres (hp-SiNSs), which consist of a porous shell and a hollow core. Upon charge/discharge cycling, the hp-SiNSs accommodate the volume change through reversible inward expansion/contraction with negligible particle-level outward expansion. Our mechanics analysis revealed that such a unique volume-change accommodation mechanism is enabled by the much stiffer modulus of the lithiated layer than the unlithiated porous layer and the low flow stress of the porous structure. Such inward expansion shields the hp-SiNSs from fracture, opposite to the outward expansion in solid Si during lithiation. Lithium ion battery assembled with this new nanoporous material exhibits high capacity, high power, long cycle life and high coulombic efficiency, which is superior to the current commercial Si-based anode materials. We find the low cost synthesis approach reported here provides a new avenue for the rational design of hierarchically porous structures with unique materials properties.

  14. Effect of the local electric field on the formation of an ordered structure in porous anodic alumina

    NASA Astrophysics Data System (ADS)

    Lazarouk, S. K.; Katsuba, P. S.; Leshok, A. A.; Vysotskii, V. B.

    2015-09-01

    Experimental data and a model are presented, and the electric field that appears in porous alumina during electrochemical anodic oxidation of aluminum in electrolytes based on an aqueous solution of oxalic acid at a voltage of 90-250 V is calculated. It is found that the electric field in the layers with a porosity of 1-10% in growing alumina reaches 109-1010 V/m, which exceeds the electric strength of the material and causes microplasma patterns emitting visible light at the pore bottom, the self-organization of the structure of porous alumina, and the anisotropy of local porous anodizing. Moreover, other new effects are to be expected during aluminum anodizing under the conditions that ensure a high electric field inside the barrier layer of porous oxide.

  15. Structural evolution and adhesion of titanium oxide film containing phosphorus and calcium on titanium by anodic oxidation.

    PubMed

    Lin, C S; Chen, M T; Liu, J H

    2008-05-01

    This study investigated the microstructure evolution and defects of the titanium oxide layer containing calcium (Ca) and phosphorus (P) formed by anodic oxidation in a solution containing Ca and P compounds. Results show that the anodic film exhibited a two-layer structure: a pore-containing amorphous titanium oxide layer dispersed with nano-sized crystallites formed prior to sparking, and a porous overlay dotted with craters formed after sparking. Ca and P were predominantly incorporated in the porous overlay, in which the amorphous region contained more Ca and P than the crystalline region regardless of the anodizing voltages. Moreover, the ratio of amorphous to crystalline regions in the porous overlay changed insignificantly with anodizing voltage. Increasing anodizing voltage enhanced the incorporation of Ca and P in the anodic film, but deteriorated the adhesion of the anodic film to the substrate. This deterioration was related to two inherent adhesive weaknesses: the aligned pores in the titanium oxide layer and the craters in the major overlay, signifying that a new anodic oxidation process that can produce high Ca- and P-containing oxide film at relatively-low anodizing voltages, i.e. approximately 200 V, is a necessity. PMID:17688247

  16. Inward lithium-ion breathing of hierarchically porous silicon anodes.

    PubMed

    Xiao, Qiangfeng; Gu, Meng; Yang, Hui; Li, Bing; Zhang, Cunman; Liu, Yang; Liu, Fang; Dai, Fang; Yang, Li; Liu, Zhongyi; Xiao, Xingcheng; Liu, Gao; Zhao, Peng; Zhang, Sulin; Wang, Chongmin; Lu, Yunfeng; Cai, Mei

    2015-01-01

    Silicon has been identified as a highly promising anode for next-generation lithium-ion batteries (LIBs). The key challenge for Si anodes is large volume change during the lithiation/delithiation cycle that results in chemomechanical degradation and subsequent rapid capacity fading. Here we report a novel fabrication method for hierarchically porous Si nanospheres (hp-SiNSs), which consist of a porous shell and a hollow core. On charge/discharge cycling, the hp-SiNSs accommodate the volume change through reversible inward Li breathing with negligible particle-level outward expansion. Our mechanics analysis revealed that such inward expansion is enabled by the much stiffer lithiated layer than the unlithiated porous layer. LIBs assembled with the hp-SiNSs exhibit high capacity, high power and long cycle life, which is superior to the current commercial Si-based anode materials. The low-cost synthesis approach provides a new avenue for the rational design of hierarchically porous structures with unique materials properties. PMID:26538181

  17. Inward lithium-ion breathing of hierarchically porous silicon anodes

    NASA Astrophysics Data System (ADS)

    Xiao, Qiangfeng; Gu, Meng; Yang, Hui; Li, Bing; Zhang, Cunman; Liu, Yang; Liu, Fang; Dai, Fang; Yang, Li; Liu, Zhongyi; Xiao, Xingcheng; Liu, Gao; Zhao, Peng; Zhang, Sulin; Wang, Chongmin; Lu, Yunfeng; Cai, Mei

    2015-11-01

    Silicon has been identified as a highly promising anode for next-generation lithium-ion batteries (LIBs). The key challenge for Si anodes is large volume change during the lithiation/delithiation cycle that results in chemomechanical degradation and subsequent rapid capacity fading. Here we report a novel fabrication method for hierarchically porous Si nanospheres (hp-SiNSs), which consist of a porous shell and a hollow core. On charge/discharge cycling, the hp-SiNSs accommodate the volume change through reversible inward Li breathing with negligible particle-level outward expansion. Our mechanics analysis revealed that such inward expansion is enabled by the much stiffer lithiated layer than the unlithiated porous layer. LIBs assembled with the hp-SiNSs exhibit high capacity, high power and long cycle life, which is superior to the current commercial Si-based anode materials. The low-cost synthesis approach provides a new avenue for the rational design of hierarchically porous structures with unique materials properties.

  18. Inward lithium-ion breathing of hierarchically porous silicon anodes

    PubMed Central

    Xiao, Qiangfeng; Gu, Meng; Yang, Hui; Li, Bing; Zhang, Cunman; Liu, Yang; Liu, Fang; Dai, Fang; Yang, Li; Liu, Zhongyi; Xiao, Xingcheng; Liu, Gao; Zhao, Peng; Zhang, Sulin; Wang, Chongmin; Lu, Yunfeng; Cai, Mei

    2015-01-01

    Silicon has been identified as a highly promising anode for next-generation lithium-ion batteries (LIBs). The key challenge for Si anodes is large volume change during the lithiation/delithiation cycle that results in chemomechanical degradation and subsequent rapid capacity fading. Here we report a novel fabrication method for hierarchically porous Si nanospheres (hp-SiNSs), which consist of a porous shell and a hollow core. On charge/discharge cycling, the hp-SiNSs accommodate the volume change through reversible inward Li breathing with negligible particle-level outward expansion. Our mechanics analysis revealed that such inward expansion is enabled by the much stiffer lithiated layer than the unlithiated porous layer. LIBs assembled with the hp-SiNSs exhibit high capacity, high power and long cycle life, which is superior to the current commercial Si-based anode materials. The low-cost synthesis approach provides a new avenue for the rational design of hierarchically porous structures with unique materials properties. PMID:26538181

  19. Preparation of porous nickel-titania cermets and their application to anode materials

    SciTech Connect

    Taimatsu, H.; Kudo, K.; Kaneko, H.; Matsukaze, N.; Iwata, T.

    1995-12-31

    Porous nickel-titania cermets have been prepared as new-type anode materials for solid oxide fuel cells using the solid-state displacement reaction method. The microstructures of the cermets were interwoven aggregate-type, differently from those of conventional nickel-YSZ cermets: nickel and titania phases three-dimensionally entangled each other. These cermets revealed good properties in compatibility of thermal expansion with YSZ, strength, gas permeation and electrical conduction.

  20. Fano resonance in anodic aluminum oxide based photonic crystals

    PubMed Central

    Shang, Guo Liang; Fei, Guang Tao; Zhang, Yao; Yan, Peng; Xu, Shao Hui; Ouyang, Hao Miao; De Zhang, Li

    2014-01-01

    Anodic aluminum oxide based photonic crystals with periodic porous structure have been prepared using voltage compensation method. The as-prepared sample showed an ultra-narrow photonic bandgap. Asymmetric line-shape profiles of the photonic bandgaps have been observed, which is attributed to Fano resonance between the photonic bandgap state of photonic crystal and continuum scattering state of porous structure. And the exhibited Fano resonance shows more clearly when the sample is saturated ethanol gas than air-filled. Further theoretical analysis by transfer matrix method verified these results. These findings provide a better understanding on the nature of photonic bandgaps of photonic crystals made up of porous materials, in which the porous structures not only exist as layers of effective-refractive-index material providing Bragg scattering, but also provide a continuum light scattering state to interact with Bragg scattering state to show an asymmetric line-shape profile. PMID:24398625

  1. Variation of nanopore diameter along porous anodic alumina channels by multi-step anodization.

    PubMed

    Lee, Kwang Hong; Lim, Xin Yuan; Wai, Kah Wing; Romanato, Filippo; Wong, Chee Cheong

    2011-02-01

    In order to form tapered nanocapillaries, we investigated a method to vary the nanopore diameter along the porous anodic alumina (PAA) channels using multi-step anodization. By anodizing the aluminum in either single acid (H3PO4) or multi-acid (H2SO4, oxalic acid and H3PO4) with increasing or decreasing voltage, the diameter of the nanopore along the PAA channel can be varied systematically corresponding to the applied voltages. The pore size along the channel can be enlarged or shrunken in the range of 20 nm to 200 nm. Structural engineering of the template along the film growth direction can be achieved by deliberately designing a suitable voltage and electrolyte together with anodization time. PMID:21456152

  2. Two-dimensional porous anodic alumina for optoelectronics and photocatalytic application

    NASA Astrophysics Data System (ADS)

    Khoroshko, L. S.

    2015-11-01

    Fabrication of porous anodic alumina film structures using anodizing, sol-gel synthesis and photolithography is reported. The structures receive interest as planar waveguides due to strong photoluminescence of the embedded trivalent lanthanides. Mesoporous structures comprising sol-gel derived titania in porous anodic alumina play a role of effective catalyst for water purification.

  3. Advanced morphological analysis of patterns of thin anodic porous alumina

    SciTech Connect

    Toccafondi, C.; Stępniowski, W.J.; Leoncini, M.; Salerno, M.

    2014-08-15

    Different conditions of fabrication of thin anodic porous alumina on glass substrates have been explored, obtaining two sets of samples with varying pore density and porosity, respectively. The patterns of pores have been imaged by high resolution scanning electron microscopy and analyzed by innovative methods. The regularity ratio has been extracted from radial profiles of the fast Fourier transforms of the images. Additionally, the Minkowski measures have been calculated. It was first observed that the regularity ratio averaged across all directions is properly corrected by the coefficient previously determined in the literature. Furthermore, the angularly averaged regularity ratio for the thin porous alumina made during short single-step anodizations is lower than that of hexagonal patterns of pores as for thick porous alumina from aluminum electropolishing and two-step anodization. Therefore, the regularity ratio represents a reliable measure of pattern order. At the same time, the lower angular spread of the regularity ratio shows that disordered porous alumina is more isotropic. Within each set, when changing either pore density or porosity, both regularity and isotropy remain rather constant, showing consistent fabrication quality of the experimental patterns. Minor deviations are tentatively discussed with the aid of the Minkowski measures, and the slight decrease in both regularity and isotropy for the final data-points of the porosity set is ascribed to excess pore opening and consequent pore merging. - Highlights: • Thin porous alumina is partly self-ordered and pattern analysis is required. • Regularity ratio is often misused: we fix the averaging and consider its spread. • We also apply the mathematical tool of Minkowski measures, new in this field. • Regularity ratio shows pattern isotropy and Minkowski helps in assessment. • General agreement with perfect artificial patterns confirms the good manufacturing.

  4. Electronic currents and the formation of nanopores in porous anodic alumina

    NASA Astrophysics Data System (ADS)

    Zhu, Xu-Fei; Song, Ye; Liu, Lin; Wang, Chen-Yu; Zheng, Jie; Jia, Hong-Bing; Wang, Xin-Long

    2009-11-01

    The formation processes of barrier anodic alumina (BAA) and porous anodic alumina (PAA) are discussed in detail. The anodizing current JT within the oxide includes ionic current jion and electronic current je during the anodizing process. The jion is used to form an oxide and the je is used to give rise to oxygen gas or sparking. The je results from the impurity centers within the oxide. For a given electrolyte, the je is dependent on the impurity centers and independent of the JT. The formation of nanopores can be ascribed to the oxygen evolution within the oxide. Oxygen gas will begin to be released at the critical thickness dc. The manner of the development of PAA is in accordance with that of BAA. The differences between PAA and BAA are the magnitude of je or the continuity of oxygen evolution. There are two competitive reactions, i.e. oxide growth (\\mathrm {2Al^{3+}+3O^{2-}} \\to \\mathrm {Al_{2}O_{3}} ) and oxygen evolution (\\mathrm {2O^{2-}} \\to \\mathrm {O_{2}} {\\uparrow } +4\\rme ). The former keeps the wall of the channel lengthened, the latter keeps the channel open. By controlling the release rate of oxygen gas under different pressures, the shape of the channels can be adjusted. The present results may open up some opportunities for fabricating special templates.

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

    PubMed

    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

  6. Cellular porous anodic alumina grown in neutral organic electrolyte. 1. Structure, composition, and properties of the films

    SciTech Connect

    Liu, Y.; Alwitt, R.S.; Shimizu, K.

    2000-04-01

    Anodic alumina films with cellular porous structure grow in neutral organic electrolytes with low water content and containing ethylene glycol and a large dicarboxylic acid. An Al carboxylate precipitates in the pore and is extruded from the coating. The porous structure develops even though the current efficiency for film formation is near 95%. The coating matrix contains substantial organic material, 15 wt % by thermal analysis. It is an oxide/organic composite with higher field strength and lower dielectric constant than pure anodic alumina.

  7. Evidence for electrohydrodynamic convection as a source of spontaneous self-ordering in porous anodic alumina films.

    PubMed

    Pashchanka, Mikhail; Schneider, Jörg J

    2016-03-01

    A comparative study of self-ordering behaviour of anodic alumina films fabricated in a series of diluted (down to 0.05 M) oxalic acid electrolytes allowed developing a relationship between the supporting electrolyte concentration and self-ordering voltages for the formation of porous oxide materials. Besides its practical importance, this work elucidates some fundamental principles of porous alumina formation, e.g. it suggests that the cell patterning arises from the electrohydrodynamic (EHD) convection process rather than the interfacial tension gradients near the anode surface (Marangoni-type instability). PMID:26881337

  8. Fabrication of Porous Anodic Alumina with Ultrasmall Nanopores

    NASA Astrophysics Data System (ADS)

    Ding, Gu Qiao; Yang, Rong; Ding, Jian Ning; Yuan, Ning Yi; Zhu, Yuan Yuan

    2010-08-01

    Anodization of Al foil under low voltages of 1-10 V was conducted to obtain porous anodic aluminas (PAAs) with ultrasmall nanopores. Regular nanopore arrays with pore diameter 6-10 nm were realized in four different electrolytes under 0-30°C according to the AFM, FESEM, TEM images and current evolution curves. It is found that the pore diameter and interpore distance, as well as the barrier layer thickness, are not sensitive to the applied potentials and electrolytes, which is totally different from the rules of general PAA fabrication. The brand-new formation mechanism has been revealed by the AFM study on the samples anodized for very short durations of 2-60 s. It is discovered for the first time that the regular nanoparticles come into being under 1-10 V at the beginning of the anodization and then serve as a template layer dominating the formation of ultrasmall nanopores. Under higher potentials from 10 to 40 V, the surface nanoparticles will be less and less and nanopores transform into general PAAs.

  9. Fabrication of Porous Anodic Alumina with Ultrasmall Nanopores

    PubMed Central

    2010-01-01

    Anodization of Al foil under low voltages of 1–10 V was conducted to obtain porous anodic aluminas (PAAs) with ultrasmall nanopores. Regular nanopore arrays with pore diameter 6–10 nm were realized in four different electrolytes under 0–30°C according to the AFM, FESEM, TEM images and current evolution curves. It is found that the pore diameter and interpore distance, as well as the barrier layer thickness, are not sensitive to the applied potentials and electrolytes, which is totally different from the rules of general PAA fabrication. The brand-new formation mechanism has been revealed by the AFM study on the samples anodized for very short durations of 2–60 s. It is discovered for the first time that the regular nanoparticles come into being under 1–10 V at the beginning of the anodization and then serve as a template layer dominating the formation of ultrasmall nanopores. Under higher potentials from 10 to 40 V, the surface nanoparticles will be less and less and nanopores transform into general PAAs. PMID:20676199

  10. Porous graphene for high capacity lithium ion battery anode material

    NASA Astrophysics Data System (ADS)

    Wang, Yusheng; Zhang, Qiaoli; Jia, Min; Yang, Dapeng; Wang, Jianjun; Li, Meng; Zhang, Jing; Sun, Qiang; Jia, Yu

    2016-02-01

    Based on density functional theory calculations, we studied the Li dispersed on porous graphene (PG) for its application as Li ion battery anode material. The hybridization of Li atoms and the carbon atoms enhanced the interaction between Li atoms and the PG. With holes of specific size, the PG can provide excellent mobility with moderate barriers of 0.37-0.39 eV. The highest Li storage composite can be LiC0.75H0.38 which corresponds to a specific capacity of 2857.7 mA h/g. Both specific capacity and binding energy are significantly larger than the corresponding value of graphite, this makes PG a promising candidate for the anode material in battery applications. The interactions between the Li atoms and PG can be easily tuned by an applied strain. Under biaxial strain of 16%, the binding energy of Li to PG is increased by 17% compared to its unstrained state.

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

    NASA Astrophysics Data System (ADS)

    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.

  12. Pilot demonstration of cerium oxide coated anodes

    SciTech Connect

    Gregg, J.S.; Frederick, M.S.; Shingler, M.J.; Alcorn, T.R.

    1992-10-01

    Cu cermet anodes were tested for 213 to 614 hours with an in-situ deposited CEROX coating in a pilot cell operated by Reynolds Manufacturing Technology Laboratory. At high bath ratio ([approximately]1.5) and low current density (0.5 A/cm[sup 2]), a [ge]1 mm thick dense CEROX coating was deposited on the anodes. At lower bath ratios and higher current density, the CEROX coating was thinner and less dense, but no change in corrosion rate was noted. Regions of low current density on the anodes and sides adjacent to the carbon anode sometimes had thin or absent CEROX coatings. Problems with cracking and oxidation of the cermet substrates led to higher corrosion rates in a pilot cell than would be anticipated from lab scale results.

  13. Functional optical devices using highly ordered hole array architectures of anodic porous alumina

    NASA Astrophysics Data System (ADS)

    Masuda, Hideki; Kondo, Toshiaki; Nishio, Kazuyuki

    2011-12-01

    The fabrication of highly ordered anodic porous alumina and its application to the fabrication of several types of functional optical devices are described. Highly ordered hole array structures of anodic porous alumina, which were formed under appropriate anodizing conditions, were applied as a starting structure in several processes for the fabrication of ordered structures used for the functional optical devices. On the basis of these processes, twodimensional photonic crystals and localized surface plasmonic devices were prepared.

  14. The thermomechanical stability of micro-solid oxide fuel cells fabricated on anodized aluminum oxide membranes

    NASA Astrophysics Data System (ADS)

    Kwon, Chang-Woo; Lee, Jae-Il; Kim, Ki-Bum; Lee, Hae-Weon; Lee, Jong-Ho; Son, Ji-Won

    2012-07-01

    The thermomechanical stability of micro-solid oxide fuel cells (micro-SOFCs) fabricated on an anodized aluminum oxide (AAO) membrane template is investigated. The full structure consists of the following layers: AAO membrane (600 nm)/Pt anode/YSZ electrolyte (900 nm)/porous Pt cathode. The utilization of a 600-nm-thick AAO membrane significantly improves the thermomechanical stability due to its well-known honeycomb-shaped nanopore structure. Moreover, the Pt anode layer deposited in between the AAO membrane and the YSZ electrolyte preserves its integrity in terms of maintaining the triple-phase boundary (TPB) and electrical conductivity during high-temperature operation. Both of these results guarantee thermomechanical stability of the micro-SOFC and extend the cell lifetime, which is one of the most critical issues in the fabrication of freestanding membrane-type micro-SOFCs.

  15. Use of Ionic Liquid in Fabrication, Characterization, and Processing of Anodic Porous Alumina

    PubMed Central

    2009-01-01

    Two different ionic liquids have been tested in the electrochemical fabrication of anodic porous alumina in an aqueous solution of oxalic acid. It was found that during galvanostatic anodization of the aluminum at a current density of 200 mA/cm2, addition of 0.5% relative volume concentration of 1-butyl-3-methylimidazolium tetrafluoborate resulted in a three-fold increase of the growth rate, as compared to the bare acidic solution with the same acid concentration. This ionic liquid was also used successfully for an assessment of the wettability of the outer surface of the alumina, by means of liquid contact angle measurements. The results have been discussed and interpreted with the aid of atomic force microscopy. The observed wetting property allowed to use the ionic liquid for protection of the pores during a test removal of the oxide barrier layer. PMID:20596395

  16. Impact of anode microstructure on solid oxide fuel cells.

    PubMed

    Suzuki, Toshio; Hasan, Zahir; Funahashi, Yoshihiro; Yamaguchi, Toshiaki; Fujishiro, Yoshinobu; Awano, Masanobu

    2009-08-14

    We report a correlation between the microstructure of the anode electrode of a solid oxide fuel cell (SOFC) and its electrochemical performance for a tubular design. It was shown that the electrochemical performance of the cell was extensively improved when the size of constituent particles was reduced so as to yield a highly porous microstructure. The SOFC had a power density of greater than 1 watt per square centimeter at an operating temperature as low as 600 degrees C with a conventional zirconia-based electrolyte, a nickel cermet anode, and a lanthanum ferrite perovskite cathode material. The effect of the hydrogen fuel flow rate (linear velocity) was also examined for the optimization of operating conditions. Higher linear fuel velocity led to better cell performance for the cell with higher anode porosity. A zirconia-based cell could be used for a low-temperature SOFC system under 600 degrees C just by optimizing the microstructure of the anode electrode and operating conditions. PMID:19679808

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

    NASA Astrophysics Data System (ADS)

    Pu, Lin; Chen, Zhi-Qiang; Tan, Chao; Yang, Zheng; Zou, Jian-Ping; Bao, Xi-Mao; Feng, Duan; Shi, Yi; Zheng, You-Dou

    2002-03-01

    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.

  18. Osseointegration of multiphase anodic spark deposition treated porous titanium implants in an ovine model.

    PubMed

    Bertollo, Nicky; Sandrini, Enrico; Dalla Pria, Paolo; Walsh, William R

    2015-03-01

    Modification of titanium oxide by multiphase anodic spark deposition (ASD) has the potential to increase bioactivity and hasten osseointegration and biological fixation in uncemented arthroplasty. This study assessed the in vivo performance of control (Ti), plasma-sprayed HA-coated (TiHA) and ASD (Biospark) treated (TiAn) porous titanium implants with a solid core using a standard uncemented implant fixation sheep model. Cortical interfacial shear-strength and bone ingrowth in cortical and cancellous sites were quantified following 12 weeks in situ. Ultimate shear-strength for the Ti, TiHA and TiAn coatings was 33±9.5, 35.4±8.4 and 33.8±7.8 MPa, respectively, which was limited by coating delamination. ASD treatment was associated with significantly higher mean bone ingrowth at both sites. These results support the osteoconductive potential of the BioSpark treatment of porous titanium. PMID:25540993

  19. Mathematical modeling of sustainability of porous Al2O3 growth during two-stage anodization process

    NASA Astrophysics Data System (ADS)

    Aryslanova, Elizaveta M.; Alfimov, Anton V.; Chivilikhin, Sergey A.

    2015-06-01

    Currently, due to the development of nanotechnology and metamaterials, it has become important to obtain regular nanoporous structures with different parameters, such as porous anodic alumina films that are used for synthesis of various nanocomposites. In this work we consider the motion of the interfaces between electrolyte and alumina layers, and between alumina and aluminum layers. We also took into account the dynamics of moving boundaries and the change of small perturbations of these boundaries. Each area under Laplace's equation is solved for the potential of the electric field. The growth of porous alumina is described with the theory of small perturbations. Small perturbations of the interface are considered, which lead to small changes in potential and current in the boundaries. As a result of the developed model we obtained the minimum distance between centers of aluminum oxide pores in the beginning of anodizing process and the wavelength of porous structure irregularities.

  20. Nanoscale Porous Lithium Titanate Anode for Superior High Temperature Performance.

    PubMed

    Alaboina, Pankaj K; Ge, Yeqian; Uddin, Md-Jamal; Liu, Yang; Lee, Dongsuek; Park, Seiung; Zhang, Xiangwu; Cho, Sung-Jin

    2016-05-18

    In this work, nanoscale porous lithium titanate (LTO) anode material was synthesized by using aqueous spray drying method after ball milling. The size of the LTO nanoparticles was optimized to 200 nm because of its considerable moisture absorption levels for stable performance and its cooperation to make good quality electrodes found with testing. The electrochemical performance of the synthesized LTO nanoparticles was found to be very stable at high operating temperature (50 °C) and high current rate (5 C) which was worth noticing than its usual unfavorable behaviors (gas generation and surface phase transitions) at higher temperatures. In the postanalysis on the aged LTO cells, high-resolution-transmission electron microscope (HRTEM) and fast Fourier transform (FFT) measurements reveal that the LTO phase transitions are maintained to very thin surface level (3-5 nm) even after 500 cycles at 50 °C. Moreover, the synthesized LTO material showed stable cycling with a high capacity of 138.74 mA h g(-1) at 1 C rate and 111.53 mA h g(-1) at 5 C rate. Furthermore, high columbic efficiency and excellent capacity retention over 500 cycles at 50 °C was achieved. The enhanced electrochemical properties can be attributed to the increase in surface area and shortened Li(+) diffusion lengths because of the nanoscale primary particles and porous structure of the synthesized LTO particles. PMID:27135524

  1. Confined Porous Graphene/SnOx Frameworks within Polyaniline-Derived Carbon as Highly Stable Lithium-Ion Battery Anodes.

    PubMed

    Zhou, Dan; Song, Wei-Li; Li, Xiaogang; Fan, Li-Zhen

    2016-06-01

    Tin oxides are promising anode materials for their high theoretical capacities in rechargeable lithium-ion batteries (LIBs). However, poor stability usually limits the practical application owing to the large volume variation during the cycling process. Herein, a novel carbon confined porous graphene/SnOx framework was designed using a silica template assisted nanocasting method followed by a polyaniline-derived carbon coating process. In this process, silica served as a template to anchor SnOx nanoparticles on porous framework and polyaniline was used as the carbon source for coating on the porous graphene/SnOx framework. The synthesized carbon confined porous graphene/SnOx frameworks demonstrate substantially improved rate capacities and enhanced cycling stability as the anode materials in LIBs, showing a high reversible capacity of 907 mAh g(-1) after 100 cycles at 100 mA g(-1) and 555 mAh g(-1) after 400 cycles at 1000 mA g(-1). The remarkably improved electrochemical performance could be assigned to the unique porous architecture, which effectively solves the drawbacks of SnOx including poor electrical conductivity and undesirable volume expansion during cycling process. Consequently, such design concept for promoting SnOx performance could provide a novel stage for improving anode stability in LIBs. PMID:27169479

  2. Fabrication of anodic aluminum oxide with incorporated chromate ions

    NASA Astrophysics Data System (ADS)

    Stępniowski, Wojciech J.; Norek, Małgorzata; Michalska-Domańska, Marta; Bombalska, Aneta; Nowak-Stępniowska, Agata; Kwaśny, Mirosław; Bojar, Zbigniew

    2012-10-01

    The anodization of aluminum in 0.3 M chromic acid is studied. The influence of operating conditions (like anodizing voltage and electrolyte's temperature) on the nanoporous anodic aluminum oxide geometry (including pore diameter, interpore distance, the oxide layer thickness and pores density) is thoroughly investigated. The results revealed typical correlations of the anodic alumina nanopore geometry with operating conditions, such as linear increase of pore diameter and interpore distance with anodizing voltage. The anodic aluminum oxide is characterized by a low pores arrangement, as determined by Fast Fourier transforms analyses of the FE-SEM images, which translates into a high concentration of oxygen vacancies. Moreover, an optimal experimental condition where chromate ions are being successfully incorporated into the anodic alumina walls, have been determined: the higher oxide growth rate the more chromate ions are being trapped. The trapped chromate ions and a high concentration of oxygen vacancies make the anodic aluminum oxide a promising luminescent material.

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

    PubMed

    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. Electrocatalysis of anodic oxidation of ethanol

    NASA Astrophysics Data System (ADS)

    Tarasevich, M. R.; Korchagin, O. V.; Kuzov, A. V.

    2013-11-01

    The results of fundamental and applied studies in the field of electrocatalysis of anodic oxidation of ethanol in fuel cells are considered. Features of the mechanism of ethanol electrooxidation are discussed as well as the structure and electrochemical properties of the most widely used catalysts of this process. The prospects of further studies of direct ethanol fuel cells with alkaline and acidic electrolytes are outlined. The bibliography includes 166 references.

  5. Numerical simulation of the baking of porous anode carbon in a vertical flue ring furnace

    SciTech Connect

    Jacobsen, M.; Melaaen, M.C.

    1998-11-13

    The interaction of pitch pyrolysis in porous anode carbon during heating and volatiles combustion in the flue gas channel has been analyzed to gain insight in the anode baking process. A two-dimensional geometry of a flue gas channel adjacent to a porous flue gas wall, packing coke, and an anode was used for studying the effect of heating rate on temperature gradients and internal gas pressure in the anodes. The mathematical model included porous heat and mass transfer, pitch pyrolysis, combustion of volatiles, radiation, and turbulent channel flow. The mathematical model was developed through source code modification of the computational fluid dynamics code FLUENT. The model was useful for studying the effects of heating rate, geometry, and anode properties.

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

    NASA Astrophysics Data System (ADS)

    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.

  7. Microstructural coarsening effects on redox instability and mechanical damage in solid oxide fuel cell anodes

    NASA Astrophysics Data System (ADS)

    Abdeljawad, F.; Haataja, M.

    2013-11-01

    In state-of-the-art high temperature solid oxide fuel cells (SOFCs), a porous composite of nickel and yttria stabilized zirconia (Ni/YSZ) is employed as the anode. The rapid oxidation of Ni into NiO is regarded as the main cause of the so-called reduction-oxidation (redox) instability in Ni/YSZ anodes, due to the presence of extensive bulk volume changes associated with this reaction. As a consequence, the development of internal stresses can lead to performance degradation and/or structural failure. In this study, we employ a recently developed continuum formalism to quantify the mechanical deformation behavior and evolution of internal stresses in Ni/YSZ porous anodes due to re-oxidation. In our approach, a local failure criterion is coupled to the continuum framework in order to account for the heterogeneous damage accumulation in the YSZ phase. The hallmark of our approach is the ability to track the spatial evolution of mechanical damage and capture the interaction of YSZ damaged regions with the local microstructure. Simulation results highlight the importance of the microstructure characterized by Ni to YSZ particle size ratio on the redox behavior and damage accumulation in as-synthesized SOFC anode systems. Moreover, a redox-strain-to-failure criterion is developed to quantify the degree by which coarsened anode microstructures become more susceptible to mechanical damage during re-oxidation.

  8. Analysis of gene expression on anodic porous alumina microarrays

    PubMed Central

    Nicolini, Claudio; Singh, Manjul; Spera, Rosanna; Felli, Lamberto

    2013-01-01

    This paper investigates the application of anodic porous alumina as an advancement on chip laboratory for gene expressions. The surface was prepared by a suitable electrolytic process to obtain a regular distribution of deep micrometric holes and printed bypen robot tips under standard conditions. The gene expression within the Nucleic Acid Programmable Protein Array (NAPPA) is realized in a confined environment of 16 spots, containing circular DNA plasmids expressed using rabbit reticulocyte lysate. Authors demonstrated the usefulness of APA in withholding the protein expression by detecting with a CCD microscope the photoluminescence signal emitted from the complex secondary antibody anchored to Cy3 and confined in the pores. Friction experiments proved the mechanical resistance under external stresses by the robot tip pens printing. So far, no attempts have been made to directly compare APA with any other surface/substrate; the rationale for pursuing APA as a potential surface coating is that it provides advantages over the simple functionalization of a glass slide, overcoming concerns about printing and its ability to generate viable arrays. PMID:23783000

  9. Stimulated emission from aluminium anode oxide films doped with rhodamine 6G

    NASA Astrophysics Data System (ADS)

    Ibrayev, N. Kh; Zeinidenov, A. K.; Aimukhanov, A. K.; Napolskii, K. S.

    2015-07-01

    The spectral and luminescent properties of the rhodamine 6G dye in a porous matrix of aluminium anode oxide are studied. The films with a highly-ordered porous structure are produced using the method of two-stage anodic oxidation. By means of raster electron microscopy it is found that the diameter of the pores amounts to nearly 50 nm and the separation between the adjacent channels is almost 105 nm. The thickness of the films is equal to 55 μm, and the specific surface area measured using the method of nitrogen capillary condensation is 15.3 m2 g-1. Fluorescence and absorption spectra of rhodamine 6G molecules injected into the pores of the aluminium anode oxide are measured. It is found that under the excitation of samples with the surface dye concentration 0.3 × 1014 molecules m-2 by the second harmonic of the Nd : YAG laser in the longitudinal scheme with the pumping intensity 0.4 MW cm-2, a narrow band of stimulated emission with the intensity maximum at the wavelength 572 nm appears against the background of the laser-induced fluorescence spectrum. A further increase in the pumping radiation intensity leads to the narrowing of the stimulated emission band and an increase in its intensity. The obtained results demonstrate the potential possibility of using the porous films of aluminium anode oxide, doped with laser dyes, in developing active elements for quantum electronics.

  10. Electrochemical reduction of UO2 in LiCl-Li2O molten salt using porous and nonporous anode shrouds

    NASA Astrophysics Data System (ADS)

    Choi, Eun-Young; Won, Chan Yeon; Cha, Ju-Sun; Park, Wooshin; Im, Hun Suk; Hong, Sun-Seok; Hur, Jin-Mok

    2014-01-01

    Electrochemical reductions of uranium oxide in a molten LiCl-Li2O electrolyte were carried out using porous and nonporous anode shrouds. The study focused on the effect of the type of anode shroud on the current density by running experiments with six anode shrouds. Dense ceramics, MgO, and MgO (3 wt%) stabilized ZrO2 (ZrO2-MgO) were used as nonporous shrouds. STS 20, 100, and 300 meshes and ZrO2-MgO coated STS 40 mesh were used as porous shrouds. The current densities (0.34-0.40 A cm-2) of the electrolysis runs using the nonporous anode shrouds were much lower than those (0.76-0.79 A cm-2) of the runs using the porous shrouds. The ZrO2-MgO shroud (600-700 MPa at 25 °C) showed better bending strength than that of MgO (170 MPa at 25 °C). The high current densities achieved in the electrolysis runs using the porous anode shrouds were attributed to the transport of O2- ions through the pores in meshes of the shroud wall. ZrO2-MgO coating on STS mesh was chemically unstable in a molten LiCl-Li2O electrolyte containing Li metal. The electrochemical reduction runs using STS 20, 100, and 300 meshes showed similar current densities in spite of their different opening sizes. The STS mesh shrouds which were immersed in a LiCl-Li2O electrolyte were stable without any damage or corrosion.

  11. Ordered three-dimensional interconnected nanoarchitectures in anodic porous alumina.

    PubMed

    Martín, Jaime; Martín-González, Marisol; Francisco Fernández, Jose; Caballero-Calero, Olga

    2014-01-01

    Three-dimensional (3D) nanostructures combine properties of nanoscale materials with the advantages of being macro-sized pieces when the time comes to manipulate, measure their properties or make a device. However, the amount of compounds with the ability to self-organize in ordered 3D nanostructures is limited. Therefore, template-based fabrication strategies become the key approach towards 3D nanostructures. Here we report the simple fabrication of a template based on anodic aluminium oxide, having a well-defined, ordered, tunable, homogeneous 3D nanotubular network in the sub 100-nm range. The 3D templates are then employed to achieve 3D, ordered nanowire networks in Bi2Te3 and polystyrene. Finally, we demonstrate the photonic crystal behaviour of both the template and the polystyrene 3D nanostructure. Our approach may establish the foundations for future high-throughput, cheap, photonic materials and devices made of simple commodity plastics, metals and semiconductors. PMID:25342247

  12. Enhanced hydrogen oxidation activity and H2S tolerance of Ni-infiltrated ceria solid oxide fuel cell anodes

    NASA Astrophysics Data System (ADS)

    Mirfakhraei, Behzad; Paulson, Scott; Thangadurai, Venkataraman; Birss, Viola

    2013-12-01

    The effect of Ni infiltration into porous Gd-doped ceria (GDC) anodes on their H2 oxidation performance, with and without added 10 ppm H2S, is reported here. Porous GDC anodes (ca. 10 μm thick) were deposited on yttria stabilized zirconia (YSZ) supports and then infiltrated with catalytic amounts of a Ni nitrate solution, followed by electrochemical testing in a 3-electrode half-cell setup at 500-800 °C. Infiltration of 3 wt.% Ni into the porous GDC anode lowered the polarization resistance by up to 85%, affecting mainly the low frequency impedance arc. When exposed to 10 ppm H2S, the Ni-infiltrated anodes exhibited a ca. 5 times higher tolerance toward sulfur poisoning compared to GDC anodes alone, also showing excellent long-term stability in 10 ppm H2S. In the presence of H2S, it is proposed that Ni, likely distributed as a nanophase, helps to maintain a clean GDC surface at the Ni/GDC interface at which the H2 oxidation reaction takes place. In turn, the GDC will readily supply oxygen anions to the adjacent Ni surfaces, thus helping to remove adsorbed sulfur.

  13. Electrochemical coating of dental implants with anodic porous titania for enhanced osteointegration

    PubMed Central

    Shayganpour, Amirreza; Rebaudi, Alberto; Cortella, Pierpaolo; Diaspro, Alberto

    2015-01-01

    Summary Clinical long-term osteointegration of titanium-based biomedical devices is the main goal for both dental and orthopedical implants. Both the surface morphology and the possible functionalization of the implant surface are important points. In the last decade, following the success of nanostructured anodic porous alumina, anodic porous titania has also attracted the interest of academic researchers. This material, investigated mainly for its photocatalytic properties and for applications in solar cells, is usually obtained from the anodization of ultrapure titanium. We anodized dental implants made of commercial grade titanium under different experimental conditions and characterized the resulting surface morphology with scanning electron microscopy equipped with an energy dispersive spectrometer. The appearance of nanopores on these implants confirm that anodic porous titania can be obtained not only on ultrapure and flat titanium but also as a conformal coating on curved surfaces of real objects made of industrial titanium alloys. Raman spectroscopy showed that the titania phase obtained is anatase. Furthermore, it was demonstrated that by carrying out the anodization in the presence of electrolyte additives such as magnesium, these can be incorporated into the porous coating. The proposed method for the surface nanostructuring of biomedical implants should allow for integration of conventional microscale treatments such as sandblasting with additive nanoscale patterning. Additional advantages are provided by this material when considering the possible loading of bioactive drugs in the porous cavities. PMID:26665091

  14. Effects of anodizing parameters and heat treatment on nanotopographical features, bioactivity, and cell culture response of additively manufactured porous titanium.

    PubMed

    Amin Yavari, S; Chai, Y C; Böttger, A J; Wauthle, R; Schrooten, J; Weinans, H; Zadpoor, A A

    2015-06-01

    Anodizing could be used for bio-functionalization of the surfaces of titanium alloys. In this study, we use anodizing for creating nanotubes on the surface of porous titanium alloy bone substitutes manufactured using selective laser melting. Different sets of anodizing parameters (voltage: 10 or 20V anodizing time: 30min to 3h) are used for anodizing porous titanium structures that were later heat treated at 500°C. The nanotopographical features are examined using electron microscopy while the bioactivity of anodized surfaces is measured using immersion tests in the simulated body fluid (SBF). Moreover, the effects of anodizing and heat treatment on the performance of one representative anodized porous titanium structures are evaluated using in vitro cell culture assays using human periosteum-derived cells (hPDCs). It has been shown that while anodizing with different anodizing parameters results in very different nanotopographical features, i.e. nanotubes in the range of 20 to 55nm, anodized surfaces have limited apatite-forming ability regardless of the applied anodizing parameters. The results of in vitro cell culture show that both anodizing, and thus generation of regular nanotopographical feature, and heat treatment improve the cell culture response of porous titanium. In particular, cell proliferation measured using metabolic activity and DNA content was improved for anodized and heat treated as well as for anodized but not heat-treated specimens. Heat treatment additionally improved the cell attachment of porous titanium surfaces and upregulated expression of osteogenic markers. Anodized but not heat-treated specimens showed some limited signs of upregulated expression of osteogenic markers. In conclusion, while varying the anodizing parameters creates different nanotube structure, it does not improve apatite-forming ability of porous titanium. However, both anodizing and heat treatment at 500°C improve the cell culture response of porous titanium. PMID

  15. Chemical Dealloying Derived 3D Porous Current Collector for Li Metal Anodes.

    PubMed

    Yun, Qinbai; He, Yan-Bing; Lv, Wei; Zhao, Yan; Li, Baohua; Kang, Feiyu; Yang, Quan-Hong

    2016-08-01

    A 3D porous Cu current collector is fabricated through chemical dealloying from a commerial Cu-Zn alloy tape. The interlinked porous framework naturally integrated can accommodate Li deposition, suppressing dendrite growth and alleviating the huge volume change during cycling. The Li metal anode combined with such a porous Cu collector demonstrates excellent performance and commerial potentials in Li-based secondary batteries. PMID:27219349

  16. Rapid fabrication of self-ordered porous alumina with 10-/sub-10-nm-scale nanostructures by selenic acid anodizing.

    PubMed

    Nishinaga, Osamu; Kikuchi, Tatsuya; Natsui, Shungo; Suzuki, Ryosuke O

    2013-01-01

    Anodic porous alumina has been widely investigated and used as a nanostructure template in various nanoapplications. The porous structure consists of numerous hexagonal cells perpendicular to the aluminum substrate and each cell has several tens or hundreds of nanoscale pores at its center. Because the nanomorphology of anodic porous alumina is limited by the electrolyte during anodizing, the discovery of additional electrolytes would expand the applicability of porous alumina. In this study, we report a new self-ordered nanoporous alumina formed by selenic acid (H2SeO4) anodizing. By optimizing the anodizing conditions, anodic alumina possessing 10-nm-scale pores was rapidly assembled (within 1 h) during selenic acid anodizing without any special electrochemical equipment. Novel sub-10-nm-scale spacing can also be achieved by selenic acid anodizing and metal sputter deposition. Our new nanoporous alumina can be used as a nanotemplate for various nanostructures in 10-/sub-10-nm-scale manufacturing. PMID:24067318

  17. Effects of the Use of Pore Formers on Performance of an Anode supported Solid Oxide Fuel Cell

    SciTech Connect

    Haslam, J J; Pham, A; Chung, B W; DiCarlo, J F; Glass, R S

    2003-12-04

    The effects of amount of pore former used to produce porosity in the anode of an anode supported planar solid oxide fuel cell were examined. The pore forming material utilized was rice starch. The reduction rate of the anode material was measured by Thermogravimetric Analysis (TGA) to qualitatively characterize the gas transport within the porous anode materials. Fuel cells with varying amounts of porosity produced by using rice starch as a pore former were tested. The performance of the fuel cell was the greatest with an optimum amount of pore former used to create porosity in the anode. This optimum is believed to be related to a trade off between increasing gas diffusion to the active three-phase boundary region of the anode and the loss of performance due to the replacement of active three-phase boundary regions of the anode with porosity.

  18. Highly porous nickel@carbon sponge as a novel type of three-dimensional anode with low cost for high catalytic performance of urea electro-oxidation in alkaline medium

    NASA Astrophysics Data System (ADS)

    Ye, Ke; Zhang, Dongming; Guo, Fen; Cheng, Kui; Wang, Guiling; Cao, Dianxue

    2015-06-01

    Highly porous nickel@carbon sponge electrode with low cost is synthesized via a facile sponge carbonization method coupled with a direct electrodeposition of Ni. The obtained electrodes are characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDX). The catalytic performances of urea electro-oxidation in alkaline medium are investigated by cyclic voltammetry (CV) and chronoamperometry (CA). The Ni@carbon sponge electrode exhibits three-dimensional open network structures with a large surface area. Remarkably, the Ni@carbon sponge electrode shows much higher electrocatalytic activity and lower onset oxidation potential towards urea electro-oxidation compared to a Ni/Ti flat electrode synthesized by the same procedure. The Ni@carbon sponge electrode achieves an onset oxidation potential of 0.24 V (vs. Ag/AgCl) and a peak current density of 290 mA cm-2 in 5 mol L-1 NaOH and 0.10 mol L-1 urea solutions accompanied with a desirable stability. The impressive electrocatalytic activity is largely attributed to the high intrinsic electronic conductivity, superior porous network structures and rich surface Ni active species, which can largely boost the interfacial electroactive sites and charge transfer rates for urea electro-oxidation in alkaline medium, indicating promising applications in fuel cells.

  19. Effects of Complex Structured Anodic Oxide Dielectric Layer Grown in Pore Matrix for Aluminum Capacitor.

    PubMed

    Shin, Jin-Ha; Yun, Sook Young; Lee, Chang Hyoung; Park, Hwa-Sun; Suh, Su-Jeong

    2015-11-01

    Anodization of aluminum is generally divided up into two types of anodic aluminum oxide structures depending on electrolyte type. In this study, an anodization process was carried out in two steps to obtain high dielectric strength and break down voltage. In the first step, evaporated high purity Al on Si wafer was anodized in oxalic acidic aqueous solution at various times at a constant temperature of 5 degrees C. In the second step, citric acidic aqueous solution was used to obtain a thickly grown sub-barrier layer. During the second anodization process, the anodizing potential of various ranges was applied at room temperature. An increased thickness of the sub-barrier layer in the porous matrix was obtained according to the increment of the applied anodizing potential. The microstructures and the growth of the sub-barrier layer were then observed with an increasing anodizing potential of 40 to 300 V by using a scanning electron microscope (SEM). An impedance analyzer was used to observe the change of electrical properties, including the capacitance, dissipation factor, impedance, and equivalent series resistance (ESR) depending on the thickness increase of the sub-barrier layer. In addition, the breakdown voltage was measured. The results revealed that dielectric strength was improved with the increase of sub-barrier layer thickness. PMID:26726615

  20. Ordered three-dimensional interconnected nanoarchitectures in anodic porous alumina

    PubMed Central

    Martín, Jaime; Martín-González, Marisol; Fernández, Jose Francisco; Caballero-Calero, Olga

    2014-01-01

    Three-dimensional nanostructures combine properties of nanoscale materials with the advantages of being macro-sized pieces when the time comes to manipulate, measure their properties, or make a device. However, the amount of compounds with the ability to self-organize in ordered three-dimensional nanostructures is limited. Therefore, template-based fabrication strategies become the key approach towards three-dimensional nanostructures. Here we report the simple fabrication of a template based on anodic aluminum oxide, having a well-defined, ordered, tunable, homogeneous 3D nanotubular network in the sub 100 nm range. The three-dimensional templates are then employed to achieve three-dimensional, ordered nanowire-networks in Bi2Te3 and polystyrene. Lastly, we demonstrate the photonic crystal behavior of both the template and the polystyrene three-dimensional nanostructure. Our approach may establish the foundations for future high-throughput, cheap, photonic materials and devices made of simple commodity plastics, metals, and semiconductors. PMID:25342247

  1. Electrochemical oxidation of phenol using graphite anodes

    SciTech Connect

    Awad, Y.M.; Abuzaid, N.S.

    1999-02-01

    The effects of current and pH on the electrochemical oxidation of phenol on graphite electrodes is investigated in this study. There was no sign of deterioration of the graphite bed after 5 months of operation. Phenol removal efficiency was a function of the current applied and was around 70% at a current of 2.2 A. The increase of phenol removal efficiency with current is attributed to the increase of ionic transport which increases the rate of electrode reactions responsible for the removal process. The percentage of complete oxidation of phenol increases with current, with a maximum value of about 50%. However, at pH 0.2 it is slightly higher than that at pH 0.5 at all currents. The phenol removal rate increases with increases of current and pH. While the current (CO{sub 2}) efficiency reaches a maximum value in the current range of 1.0--1.2 A, it increases with an increase of acid concentration. The findings of this study have important implications: while anodic oxidation of phenol on graphite can achieve acceptable removal of phenol, the extent of oxidation should not be overlooked.

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

    NASA Astrophysics Data System (ADS)

    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. Porous Si spheres encapsulated in carbon shells with enhanced anodic performance in lithium-ion batteries

    SciTech Connect

    Wang, Hui; Wu, Ping Shi, Huimin; Lou, Feijian; Tang, Yawen; Zhou, Tongge; Zhou, Yiming Lu, Tianhong

    2014-07-01

    Highlights: • In situ magnesiothermic reduction route for the formation of porous Si@C spheres. • Unique microstructural characteristics of both porous sphere and carbon matrix. • Enhanced anodic performance in term of cycling stability for lithium-ion batteries. - Abstract: A novel type of porous Si–C micro/nano-hybrids, i.e., porous Si spheres encapsulated in carbon shells (porous Si@C spheres), has been constructed through the pyrolysis of polyvinylidene fluoride (PVDF) and subsequent magnesiothermic reduction methodology by using SiO{sub 2} spheres as precursors. The as-synthesized porous Si@C spheres have been applied as anode materials for lithium-ion batteries (LIBs), and exhibit enhanced anodic performance in term of cycling stability compared with bare Si spheres. For example, the porous Si@C spheres are able to exhibit a high reversible capacity of 900.0 mA h g{sup −1} after 20 cycles at a current density of 0.05 C (1 C = 4200 mA g{sup −1}), which is much higher than that of bare Si spheres (430.7 mA h g{sup −1})

  4. Pore-Scale Investigation of Mass Transport and Electrochemistry in a Solid Oxide Fuel Cell Anode

    SciTech Connect

    Grew, Kyle N.; Joshi, Abhijit S.; Peracchio, Aldo A.; Chiu, Wilson K. S.

    2009-10-31

    The development and validation of a model for the study of pore-scale transport phenomena and electrochemistry in a Solid Oxide Fuel Cell (SOFC) anode are presented in this work. This model couples mass transport processes with a detailed reaction mechanism, which is used to model the electrochemical oxidation kinetics. Detailed electrochemical oxidation reaction kinetics, which is known to occur in the vicinity of the three-phase boundary (TPB) interfaces, is discretely considered in this work. The TPB regions connect percolating regions of electronic and ionic conducting phases of the anode, nickel (Ni) and yttria-stabilized zirconia (YSZ), respectively; with porous regions supporting mass transport of the fuel and product. A two-dimensional (2D), multi-species lattice Boltzmann method (LBM) is used to describe the diffusion process in complex pore structures that are representative of the SOFC anode. This diffusion model is discretely coupled to a kinetic electrochemical oxidation mechanism using localized flux boundary conditions. The details of the oxidation kinetics are prescribed as a function of applied activation overpotential and the localized hydrogen and water mole fractions. This development effort is aimed at understanding the effects of the anode microstructure within TPB regions. This work describes the methods used so that future studies can consider the details of SOFC anode microstructure.

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

    NASA Technical Reports Server (NTRS)

    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.

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

    NASA Technical Reports Server (NTRS)

    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.

  7. Highly Ordered Porous Anodic Alumina with Large Diameter Pores Fabricated by an Improved Two-Step Anodization Approach.

    PubMed

    Li, Xiaohong; Ni, Siyu; Zhou, Xingping

    2015-02-01

    The aim of this study is to prepare highly ordered porous anodic alumina (PAA) with large pore sizes (> 200 nm) by an improved two-step anodization approach which combines the first hard anodization in oxalic acid-water-ethanol system and second mild anodization in phosphoric acid-water-ethanol system. The surface morphology and elemental composition of PAA are characterized by field emission scanning electron microscopy (FESEM) and energy-dispersive X-ray spectrometer (EDS). The effects of matching of two-step anodizing voltages on the regularity of pore arrangement is evaluated and discussed. Moreover, the pore formation mechanism is also discussed. The results show that the nanopore arrays on all the PAA samples are in a highly regular arrangement and the pore size is adjustable in the range of 200-300 nm. EDS analysis suggests that the main elements of the as-prepared PAA are oxygen, aluminum and a small amount of phosphorus. Furthermore, the voltage in the first anodization must match well with that in the second anodization, which has significant influence on the PAA regularity. The addition of ethanol to the electrolytes effectively accelerates the diffusion of the heat that evolves from the sample, and decreases the steady current to keep the steady growth of PAA film. The improved two-step anodization approach in this study breaks through the restriction of small pore size in oxalic acid and overcomes the drawbacks of irregular pore morphology in phosphoric acid, and is an efficient way to fabricate large diameter ordered PAA. PMID:26353721

  8. Atomic force microscopy and anodic porous allumina of nucleic acid programmable protein arrays.

    PubMed

    Nicolini, Claudio; Correia, Tercio Bezerra; Stura, Enrico; Larosa, Claudio; Spera, Rosanna; Pechkova, Eugenia

    2013-08-01

    The methodological aspects are here presented for the NAPPA (Nucleic Acid Programmable Protein Arrays) characterization by atomic force microscopy and anodic porous alumina. Anodic Porous Alumina represents also an advanced on chip laboratory for gene expression contained in an engineered plasmid vector. The results obtained with CdK2, CDKN1A, p53 and Jun test genes expressed on NAPPA and the future developments are discussed in terms of our pertinent and recent Patents and of their possibility to overcome some limitations of present fluorescence detection in probing protein-protein interaction in both basic sciences and clinical studies. PMID:23848275

  9. Evolution of insoluble eutectic Si particles in anodic oxidation films during adipic-sulfuric acid anodizing processes of ZL114A aluminum alloys

    NASA Astrophysics Data System (ADS)

    Hua, Lei; Liu, Jian-hua; Li, Song-mei; Yu, Mei; Wang, Lei; Cui, Yong-xin

    2015-03-01

    The effects of insoluble eutectic Si particles on the growth of anodic oxide films on ZL114A aluminum alloy substrates were investigated by optical microscopy (OM) and scanning electron microscopy (SEM). The anodic oxidation was performed at 25°C and a constant voltage of 15 V in a solution containing 50 g/L sulfuric acid and 10 g/L adipic acid. The thickness of the formed anodic oxidation film was approximately 7.13 μm. The interpore distance and the diameters of the major pores in the porous layer of the film were within the approximate ranges of 10-20 nm and 5-10 nm, respectively. Insoluble eutectic Si particles strongly influenced the morphology of the anodic oxidation films. The anodic oxidation films exhibited minimal defects and a uniform thickness on the ZL114A substrates; in contrast, when the front of the oxide oxidation films encountered eutectic Si particles, defects such as pits and non-uniform thickness were observed, and pits were observed in the films.

  10. Simulation of Flow Through Porous Anode in Mfc at Higher Power Density

    NASA Astrophysics Data System (ADS)

    Su, W. W.; Xu, Y. S.; Yan, W. W.; Liu, Y.

    Microbial fuel cell (MFC) is a new environmental friendly energy device which has received greatly attention due to its technology for producing electricity directly from organic or inorganic matter using bacteria as catalyst. To date, many studies have been carried out on advective flow through porous anode in a continuous flow MFC. However, the precise mechanical mechanism of flow through porous anode and the quantified relationship between porous media and MFC performance are not yet clearly understood. It has been found experimentally the power density can be increased apparently at certain spacing configuration. Based on these available experimental data, we studied the effect of spacing between electrodes and the Darcy number of porous anode on the power generation performance of MFC using lattice Boltzmann method. The simulation results indicated that the spacing between electrodes significantly influence the flow velocity profile and residence time in the MFC. Moreover, it was found that the Darcy number of porous anode could regulate the output efficiency of MFC. Our results would be helpful to optimize MFC design.

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

    PubMed

    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

  12. The anodic oxidation of p-benzoquinone and maleic acid

    SciTech Connect

    Bock, C.; MacDougall, B.

    1999-08-01

    The oxidation of organics, in particular of p-benzoquinone and maleic acid, at high anodic potentials has been studied using a range of anode materials such as noble-metal-based oxides and antimony-doped tin oxides. The influence of the current density was also investigated showing that the oxidation rate of p-benzoquinone increased only slightly with increasing current density. The efficiency of the p-benzoquinone oxidation was found to depend on several properties of the anode material, not just its chemical nature. Furthermore, efficiencies for the partial oxidation of p-benzoquinone using specially prepared noble-metal-oxide-based anodes were found to be only somewhat smaller or even as high as those observed for PbO{sub 2} or antimony-doped tin oxide anodes, respectively. The anodic electrolysis of maleic acid solutions was found to decrease the activity of IrO{sub 2} for the oxidation of organic compounds. This was not observed when PbO{sup 2} was employed for the oxidation of maleic acid.

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

    PubMed Central

    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

  14. Characterization of Anodic Aluminum Oxide Membrane with Variation of Crystallizing Temperature for pH Sensor.

    PubMed

    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

  15. Understanding and Shaping the Morphology of the Barrier Layer of Supported Porous Anodized Alumina on Gold Underlayers.

    PubMed

    Berger, Nele; Es-Souni, Mohammed

    2016-07-12

    Large-area ordered nanorod (NR) arrays of various functional materials can be easily and cost-effectively processed using on-substrate anodized porous aluminum oxide (PAO) films as templates. However, reproducibility in the processing of PAO films is still an issue because they are prone to delamination, and control of fabrication parameters such as electrolyte type and concentration and anodizing time is critical for making robust templates and subsequently mechanically reliable NR arrays. In the present work, we systematically investigate the effects of the fabrication parameters on pore base morphology, devise a method to avoid delamination, and control void formation under the barrier layer of PAO films on gold underlayers. Via systematic control of the anodization parameters, particularly the anodization current density and time, we follow the different stages of void development and discuss their formation mechanisms. The practical aspect of this work demonstrates how void size can be controlled and how void formation can be utilized to control the shape of NR bases for improving the mechanical stability of the NRs. PMID:27315420

  16. Hollow/porous nanostructures derived from nanoscale metal-organic frameworks towards high performance anodes for lithium-ion batteries

    NASA Astrophysics Data System (ADS)

    Hu, Lin; Chen, Qianwang

    2014-01-01

    Lithium-ion batteries (LIBs), owing to their high energy density, light weight, and long cycle life, have shown considerable promise for storage devices. The successful utilization of LIBs depends strongly on the preparation of nanomaterials with outstanding lithium storage properties. Recent progress has demonstrated that hollow/porous nanostructured oxides are very attractive candidates for LIBs anodes due to their high storage capacities. Here, we aim to provide an overview of nanoscale metal-organic frameworks (NMOFs)-templated synthesis of hollow/porous nanostructured oxides and their LIBs applications. By choosing some typical NMOFs as examples, we present a comprehensive summary of synthetic procedures for nanostructured oxides, such as binary, ternary and composite oxides. Hollow/porous structures are readily obtained due to volume loss and release of internally generated gas molecules during the calcination of NMOFs in air. Interestingly, the NMOFs-derived hollow/porous structures possess several special features: pores generated from gas molecules release will connect to each other, which are distinct from ``dead pores'' pore size often appears to be <10 nm; in terms of surface chemistry, the pore surface is hydrophobic. These structural features are believed to be the most critical factors that determine LIBs' performance. Indeed, it has been shown that these NMOFs-derived hollow/porous oxides exhibit excellent electrochemical performance as anode materials for LIBs, including high storage capacity, good cycle stability, and so on. For example, a high charge capacity of 1465 mA h g-1 at a rate of 300 mA g-1 was observed after 50 cycles for NMOFs-derived Co3O4 porous nanocages, which corresponds to 94.09% of the initial capacity (1557 mA h g-1), indicating excellent stability. The capacity of NMOFs-derived Co3O4 is higher than that of other Co3O4 nanostructures obtained by a conventional two-step route, including nanosheets (1450 mA h g-1 at 50 mA g-1

  17. Cell Adhesion and Growth on the Anodized Aluminum Oxide Membrane.

    PubMed

    Park, Jeong Su; Moon, Dalnim; Kim, Jin-Seok; Lee, Jin Seok

    2016-03-01

    Nanotopological cues are popular tools for in vivo investigation of the extracellular matrix (ECM) and cellular microenvironments. The ECM is composed of multiple components and generates a complex microenvironment. The development of accurate in vivo methods for the investigation of ECM are important for disease diagnosis and therapy, as well as for studies on cell behavior. Here, we fabricated anodized aluminum oxide (AAO) membranes using sulfuric and oxalic acid under controlled voltage and temperature. The membranes were designed to possess three different pore and interpore sizes, AAO-1, AAO-2, and AAO-3 membranes, respectively. These membranes were used as tools to investigate nanotopology-signal induced cell behavior. Cancerous cells, specifically, the OVCAR-8 cell-line, were cultured on porous AAO membranes and the effects of these membranes on cell shape, proliferation, and viability were studied. AAO-1 membranes bearing small sized pores were found to maintain the spreading shape of the cultured cells. Cells cultured on AAO-2 and AAO-3 membranes, bearing large pore-sized AAO membranes, changed shape from spreading to rounding. Furthermore, cellular area decreased when cells were cultured on all three AAO membranes that confirmed decreased levels of focal adhesion kinase (FAK). Additionally, OVCAR-8 cells exhibited increased proliferation on AAO membranes possessing various pore sizes, indicating the importance of the nanosurface structure in regulating cell behaviors, such as cell proliferation. Our results suggest that porous-AAO membranes induced nanosurface regulated cell behavior as focal adhesion altered the intracellular organization of the cytoskeleton. Our results may find potential applications as tools in in vivo cancer research studies. PMID:27280255

  18. Porous silicon based anode material formed using metal reduction

    SciTech Connect

    Anguchamy, Yogesh Kumar; Masarapu, Charan; Deng, Haixia; Han, Yongbong; Venkatachalam, Subramanian; Kumar, Sujeet; Lopez, Herman A.

    2015-09-22

    A porous silicon based material comprising porous crystalline elemental silicon formed by reducing silicon dioxide with a reducing metal in a heating process followed by acid etching is used to construct negative electrode used in lithium ion batteries. Gradual temperature heating ramp(s) with optional temperature steps can be used to perform the heating process. The porous silicon formed has a high surface area from about 10 m.sup.2/g to about 200 m.sup.2/g and is substantially free of carbon. The negative electrode formed can have a discharge specific capacity of at least 1800 mAh/g at rate of C/3 discharged from 1.5V to 0.005V against lithium with in some embodiments loading levels ranging from about 1.4 mg/cm.sup.2 to about 3.5 mg/cm.sup.2. In some embodiments, the porous silicon can be coated with a carbon coating or blended with carbon nanofibers or other conductive carbon material.

  19. Fast fabrication of self-ordered anodic porous alumina on oriented aluminum grains by high acid concentration and high temperature anodization.

    PubMed

    Cheng, Chuan; Ngan, Alfonso H W

    2013-05-31

    Anodic porous alumina, which exhibits a characteristic nanohoneycomb structure, has been used in a wide range of nanotechnology applications. The conventional fabrication method of mild anodization (MA) requires a prolonged anodization time which is impractical for batch processing, and self-ordered porous structures can only be formed within narrow processing windows so that the dimensions of the resultant structures are extremely limited. The alternative hard anodization (HA) may easily result in macroscopic defects on the alumina surface. In this work, by systematically varying the anodization conditions including the substrate grain orientation, electrolyte concentration, temperature, voltage, and time, a new oxalic acid based anodization method, called high acid concentration and high temperature anodization (HHA), is found, which can result in far better self-ordering of the porous structures at rates 7-26 times faster than MA, under a continuous voltage range of 30-60 V on (001) oriented Al grains. Unlike HA, no macroscopic defects appear under the optimum self-ordered conditions of HHA at 40 V, even for pore channels grown up to high aspect ratios of more than 3000. Compared to MA and HA, HHA provides more choices of self-ordered nano-porous structures with fast and mechanically stable formation features for practical applications. PMID:23619572

  20. Effect of processing on structural features of anodic aluminum oxides

    NASA Astrophysics Data System (ADS)

    Erdogan, Pembe; Birol, Yucel

    2012-09-01

    Morphological features of the anodic aluminum oxide (AAO) templates fabricated by electrochemical oxidation under different processing conditions were investigated. The selection of the polishing parameters does not appear to be critical as long as the aluminum substrate is polished adequately prior to the anodization process. AAO layers with a highly ordered pore distribution are obtained after anodizing in 0.6 M oxalic acid at 20 °C under 40 V for 5 minutes suggesting that the desired pore features are attained once an oxide layer develops on the surface. While the pore features are not affected much, the thickness of the AAO template increases with increasing anodization treatment time. Pore features are better and the AAO growth rate is higher at 20 °C than at 5 °C; higher under 45 V than under 40 V; higher with 0.6 M than with 0.3 M oxalic acid.

  1. Recent anode advances in solid oxide fuel cells

    NASA Astrophysics Data System (ADS)

    Sun, Chunwen; Stimming, Ulrich

    Solid oxide fuel cells (SOFCs) are electrochemical reactors that can directly convert the chemical energy of a fuel gas into electrical energy with high efficiency and in an environment-friendly way. The recent trends in the research of solid oxide fuel cells concern the use of available hydrocarbon fuels, such as natural gas. The most commonly used anode material Ni/YSZ cermet exhibits some disadvantages when hydrocarbons were used as fuels. Thus it is necessary to develop alternative anode materials which display mixed conductivity under fuel conditions. This article reviews the recent developments of anode in SOFCs with principal emphasis on the material aspects. In addition, the mechanism and kinetics of fuel oxidation reactions are also addressed. Various processes used for the cost-effective fabrication of anode have also been summarized. Finally, this review will be concluded with personal perspectives on the future research directions of this area.

  2. Electrochemical fabrication and optical properties of porous tin oxide films with structural colors

    SciTech Connect

    Cheng, Hua; Shu, Shiwei; Lee, Chris; Zeng, Shanshan; Lu, Zhouguang; Lu, Jian E-mail: yangli@cityu.edu.hk; Li, Yang Yang E-mail: yangli@cityu.edu.hk

    2014-10-21

    Photonic crystals with porous features not only provide the capability to control light but also enable structural colors that are environmentally sensitive. Here, we report a novel kind of tin oxide-based photonic crystal featuring periodically arranged air pores fabricated by the periodic anodization of tin foil. The existence of a photonic band gap in the fabricated structure is verified by its vivid color, and its reflective spectra which are responsive to environmental stimuli. Furthermore, the sample colors (i.e., the photonic band gap positions) can be easily adjusted by manipulating the anodization parameters. The theoretical modeling results of these tin oxide photonic crystals agree well with the reported experimental ones.

  3. On the anodic aluminium oxide refractive index of nanoporous templates

    NASA Astrophysics Data System (ADS)

    Hierro-Rodriguez, A.; Rocha-Rodrigues, P.; Valdés-Bango, F.; Alameda, J. M.; Jorge, P. A. S.; Santos, J. L.; Araujo, J. P.; Teixeira, J. M.; Guerreiro, A.

    2015-11-01

    In the present study, we have determined the intrinsic refractive index of anodic aluminium oxide, which is originated by the formation of nanoporous alumina templates. Different templates have been fabricated by the conventional two-step anodization procedure in oxalic acid. Their porosities were modified by chemical wet etching allowing the tuning of their effective refractive indexes (air-filled nanopores  +  anodic aluminium oxide). By standard spectroscopic light transmission measurements, the effective refractive index for each different template was extracted in the VIS-NIR region. The determination of the intrinsic anodic aluminium oxide refractive index was performed by using the Maxwell-Garnett homogenization theory. The results are coincident for all the fabricated samples. The obtained refractive index (~1.55) is quite lower (~22%) than the commonly used Al2O3 handbook value (~1.75), showing that the amorphous nature of the anodic oxide structure strongly conditions its optical properties. This difference is critical for the correct design and modeling of optical plasmonic metamaterials based on anodic aluminium oxide nanoporous templates.

  4. Novel Carbon-Encapsulated Porous SnO2 Anode for Lithium-Ion Batteries with Much Improved Cyclic Stability.

    PubMed

    Huang, Bin; Li, Xinhai; Pei, Yi; Li, Shuang; Cao, Xi; Massé, Robert C; Cao, Guozhong

    2016-04-01

    Porous SnO2 submicrocubes (SMCs) are synthesized by annealing and HNO3 etching of CoSn(OH)6 SMCs. Bare SnO2 SMCs, as well as bare commercial SnO2 nanoparticles (NPs), show very high initial discharge capacity when used as anode material for lithium-ion batteries. However, during the following cycles most of the Li ions previously inserted cannot be extracted, resulting in considerable irreversibility. Porous SnO2 cubes have been proven to possess better electrochemical performance than the dense nanoparticles. After being encapsulated by carbon shell, the obtained yolk-shell SnO2 SMCs@C exhibits significantly enhanced reversibility for lithium-ions storage. The reversibility of the conversion between SnO2 and Sn, which is largely responsible for the enhanced capacity, has been discussed. The porous SnO2 SMCs@C shows much increased capacity and cycling stability, demonstrating that the porous SnO2 core is essential for better lithium-ion storage performance. The strategy introduced in this paper can be used as a versatile way to fabrication of various metal-oxide-based composites. PMID:26882498

  5. Growth control of carbon nanotubes using by anodic aluminum oxide nano templates.

    PubMed

    Park, Yong Seob; Choi, Won Seek; Yi, Junsin; Lee, Jaehyeong

    2014-05-01

    Anodic Aluminum Oxide (AAO) template prepared in acid electrolyte possess regular and highly anisotropic porous structure with pore diameter range from five to several hundred nanometers, and with a density of pores ranging from 10(9) to 10(11) cm(-2). AAO can be used as microfilters and templates for the growth of CNTs and metal or semiconductor nanowires. Varying anodizing conditions such as temperature, electrolyte, applied voltage, anodizing and widening time, one can control the diameter, the length, and the density of pores. In this work, we deposited Al thin film by radio frequency magnetron sputtering method to fabricate AAO nano template and synthesized multi-well carbon nanotubes on a glass substrate by microwave plasma-enhanced chemical vapor deposition (MPECVD). AAO nano-porous templates with various pore sizes and depths were introduced to control the dimension and density of CNT arrays. The AAO nano template was synthesize on glass by two-step anodization technique. The average diameter and interpore distance of AAO nano template are about 65 nm and 82 nm. The pore density and AAO nano template thickness are about 2.1 x 10(10) pores/cm2 and 1 microm, respectively. Aligned CNTs on the AAO nano template were synthesized by MPECVD at 650 degrees C with the Ni catalyst layer. The length and diameter of CNTs were grown 2 microm and 50 nm, respectively. PMID:24734654

  6. Model of the radial distribution function of pores in a layer of porous aluminum oxide

    NASA Astrophysics Data System (ADS)

    Cherkas, N. L.; Cherkas, S. L.

    2016-03-01

    An empirical formula is derived to describe the quasi-periodic structure of a layer of porous aluminum oxide obtained by anodization. The formula accounts for two mechanisms of the transition from the ordered state (2D crystal) to the amorphous state. The first mechanism infers that vacancy-type defects arise, but the crystal lattice remains undestroyed. The second mechanism describes the lattice destruction. The radial distribution function of the pores in porous aluminum oxide is obtained using the Bessel transform. Comparison with a real sample is performed.

  7. Fabrication of polymeric nano-batteries array using anodic aluminum oxide templates.

    PubMed

    Zhao, Qiang; Cui, Xiaoli; Chen, Ling; Liu, Ling; Sun, Zhenkun; Jiang, Zhiyu

    2009-02-01

    Rechargeable nano-batteries were fabricated in the array pores of anodic aluminum oxide (AAO) template, combining template method and electrochemical method. The battery consisted of electropolymerized PPy electrode, porous TiO2 separator, and chemically polymerized PAn electrode was fabricated in the array pores of two-step anodizing aluminum oxide (AAO) membrane, based on three-step assembling method. It performs typical electrochemical battery behavior with good charge-discharge ability, and presents a capacity of 25 nAs. AFM results show the hexagonal array of nano-batteries' top side. The nano-battery may be a promising device for the development of Micro-Electro-Mechanical Systems (MEMS), and Nano-Electro-Mechanical Systems (NEMS). PMID:19441424

  8. Long-term cycling stability of porous Sn anode for sodium-ion batteries

    NASA Astrophysics Data System (ADS)

    Kim, Changhyeon; Lee, Ki-Young; Kim, Icpyo; Park, Jinsoo; Cho, Gyubong; Kim, Ki-Won; Ahn, Jou-Hyeon; Ahn, Hyo-Jun

    2016-06-01

    A phase-inversion technique is introduced to produce a porous Sn anode for sodium batteries, which can accommodate volume changes during sodiation and desodiation. The Sn electrode shows two plateaus with a capacity of 1066 mAh g-1 during the first sodiation and four flat plateaus with a charge capacity of 674 mAh g-1 at the first desodiation process. During 500 cycles, the Sn electrode shows reversible capacity more than 519 mAh g-1 with Coulombic efficiency of nearly 99%. The Sn electrode with a porous structure is a possible solution to the electrode degradation.

  9. Efficient suppression of nanograss during porous anodic TiO2 nanotubes growth

    NASA Astrophysics Data System (ADS)

    Gui, Qunfang; Yu, Dongliang; Li, Dongdong; Song, Ye; Zhu, Xufei; Cao, Liu; Zhang, Shaoyu; Ma, Weihua; You, Shiyu

    2014-09-01

    When Ti foil was anodized in fluoride-containing electrolyte for a long time, undesired etching-induced “nanograss” would inevitably generate on the top of porous anodic TiO2 nanotubes (PATNTs). The nanograss will hinder the ions transport and in turn yield depressed (photo) electrochemical performance. In order to obtain nanograss-free nanotubes, a modified three-step anodization and two-layer nanostructure of PATNTs were designed to avoid the nanograss. The first layer (L1) nanotubes were obtained by the conventional two-step anodization. After washing and drying processes, the third-step anodization was carried out with the presence of L1 nanotubes. The L1 nanotubes, serving as a sacrificed layer, was etched and transformed into nanograss, while the ultralong nanotubes (L2) were maintained underneath the L1. The bi-layer nanostructure of the nanograss/nanotubes (L1/L2) was then ultrasonically rinsed in deionized water to remove the nanograss (L1 layer). Then much longer nanotubes (L2 layer) with intact nanotube mouths could be obtained. Using this novel approach, the ultralong nanotubes without nanograss can be rationally controlled by adjusting the anodizing times of two layers.

  10. High-performance anode based on porous Co3O4 nanodiscs

    SciTech Connect

    Pan, Anqiang; Wang, Yaping; Xu, Wu; Nie, Zhiwei; Liang, Shuquan; Nie, Zimin; Wang, Chong M.; Cao, Guozhong; Zhang, Jiguang

    2014-06-01

    In this article, two-dimensional, Co3O4 hexagonal nanodiscs are prepared using a hydrothermal method without surfactants. X-ray diffraction (XRD), scanning electron microscopy (SEM), and transmission electron microscopy (TEM) have been employed to characterize the structural properties. As revealed by the SEM and TEM experiments, the thickness of our as-fabricated Co3O4 hexagonal nanodiscs is about 20 nm, and the pore diameters range from several nanometers to 30 nm. As an anode for lithium-ion batteries, porous Co3O4 nanodiscs exhibit an average discharge voltage of ~1 V (Vs. Li/Li+) and a high specific charge capacity of 1161 mAh g-1 after 100 cycles. They also demonstrate excellent rate performance and high Coloumbic efficiency at various rates. These results indicate that porous Co3O4 nanodiscs are good candidates as anode materials for lithium-ion batteries.

  11. A Microsystem Based on Porous Silicon-Glass Anodic Bonding for Gas and Liquid Optical Sensing

    PubMed Central

    De Stefano, Luca; Malecki, Krzysztof; Della Corte, Francesco G.; Moretti, Luigi; Rea, Ilaria; Rotiroti, Lucia; Rendina, Ivo

    2006-01-01

    We have recently presented an integrated silicon-glass opto-chemical sensor for lab-on-chip applications, based on porous silicon and anodic bonding technologies. In this work, we have optically characterized the sensor response on exposure to vapors of several organic compounds by means of reflectivity measurements. The interaction between the porous silicon, which acts as transducer layer, and the organic vapors fluxed into the glass sealed microchamber, is preserved by the fabrication process, resulting in optical path increase, due to the capillary condensation of the vapors into the pores. Using the Bruggemann theory, we have calculated the filled pores volume for each substance. The sensor dynamic has been described by time-resolved measurements: due to the analysis chamber miniaturization, the response time is only of 2 s. All these results have been compared with data acquired on the same PSi structure before the anodic bonding process.

  12. Superstructured Carbon Nanotube/Porous Silicon Hybrid Materials for Lithium-Ion Battery Anodes

    NASA Astrophysics Data System (ADS)

    Lee, Jun-Ki; Kang, Shin-Hyun; Choi, Sung-Min

    2015-03-01

    High energy Li-ion batteries (LIBs) are in great demand for electronics, electric-vehicles, and grid-scale energy storage. To further increase the energy and power densities of LIBs, Si anodes have been intensively explored due to their high capacity, and high abundance compared with traditional carbon anodes. However, the poor cycle-life caused by large volume expansion during charge/discharge process has been an impediment to its applications. Recently, superstructured Si materials were received attentions to solve above mentioned problem in excellent mechanical properties, large surface area, and fast Li and electron transportation aspects, but applying superstructures to anode is in early stage yet. Here, we synthesized superstructured carbon nanotubes (CNTs)/porous Si hybrid materials and its particular electrochemical properties will be presented. Department of Nuclear and Quantum Engineering

  13. Rapid fabrication of self-ordered porous alumina with 10-/sub-10-nm-scale nanostructures by selenic acid anodizing

    PubMed Central

    Nishinaga, Osamu; Kikuchi, Tatsuya; Natsui, Shungo; Suzuki, Ryosuke O.

    2013-01-01

    Anodic porous alumina has been widely investigated and used as a nanostructure template in various nanoapplications. The porous structure consists of numerous hexagonal cells perpendicular to the aluminum substrate and each cell has several tens or hundreds of nanoscale pores at its center. Because the nanomorphology of anodic porous alumina is limited by the electrolyte during anodizing, the discovery of additional electrolytes would expand the applicability of porous alumina. In this study, we report a new self-ordered nanoporous alumina formed by selenic acid (H2SeO4) anodizing. By optimizing the anodizing conditions, anodic alumina possessing 10-nm-scale pores was rapidly assembled (within 1 h) during selenic acid anodizing without any special electrochemical equipment. Novel sub-10-nm-scale spacing can also be achieved by selenic acid anodizing and metal sputter deposition. Our new nanoporous alumina can be used as a nanotemplate for various nanostructures in 10-/sub-10-nm-scale manufacturing. PMID:24067318

  14. Model anodes and anode models for understanding the mechanism of hydrogen oxidation in solid oxide fuel cells.

    PubMed

    Bessler, Wolfgang G; Vogler, Marcel; Störmer, Heike; Gerthsen, Dagmar; Utz, Annika; Weber, André; Ivers-Tiffée, Ellen

    2010-11-14

    This article presents a literature review and new results on experimental and theoretical investigations of the electrochemistry of solid oxide fuel cell (SOFC) model anodes, focusing on the nickel/yttria-stabilized zirconia (Ni/YSZ) materials system with operation under H(2)/H(2)O atmospheres. Micropatterned model anodes were used for electrochemical characterization under well-defined operating conditions. Structural and chemical integrity was confirmed by ex situ pre-test and post-test microstructural and chemical analysis. Elementary kinetic models of reaction and transport processes were used to assess reaction pathways and rate-determining steps. The comparison of experimental and simulated electrochemical behaviors of pattern anodes shows quantitative agreement over a wide range of operating conditions (p(H(2)) = 8×10(2) - 9×10(4) Pa, p(H(2)O) = 2×10(1) - 6×10(4) Pa, T = 400-800 °C). Previously published experimental data on model anodes show a strong scatter in electrochemical performance. Furthermore, model anodes exhibit a pronounced dynamics on multiple time scales which is not reproduced in state-of-the-art models and which is also not observed in technical cermet anodes. Potential origin of these effects as well as consequences for further steps in model anode and anode model studies are discussed. PMID:20820576

  15. Adhesion and proliferation of osteoblast-like cells on anodic porous alumina substrates with different morphology.

    PubMed

    Salerno, Marco; Caneva-Soumetz, Federico; Pastorino, Laura; Patra, Niranjan; Diaspro, Alberto; Ruggiero, Carmelina

    2013-06-01

    We have fabricated nanoporous alumina surfaces by means of anodization in oxalic acid in different conditions and used them as the substrates for the growth of cells from a human osteoblast-like cell line. The rough nanoporous alumina substrates have been compared both with smooth standard Petri dishes used as the control and with commercial substrates of similar material. The viability of the cells has been assessed at different culture times of 4, 11, 18, and 25 days in vitro. It turned out that the porous side of the galvanostatically fabricated alumina performed similar to the control and better than the commercial porous alumina, whereas the potentiostatically fabricated porous alumina performed better than all the other substrates at all times, and in particular at the two shortest time periods of 4 and 11 days in vitro. The best performance of the substrates is associated with intermediate surface roughness and feature spacing. PMID:23722279

  16. Water Decontamination With New Porous Oxide Photocatalysts

    NASA Astrophysics Data System (ADS)

    Zarei Chaleshtori, M.; Saupe, G. B.

    2008-12-01

    Water pollution is major environmental problem worldwide. Many common industrial organic compounds that make their way into water systems can be carcinogenic at trace levels and are difficult and costly to remove completely with conventional technologies. Heterogeneous photocatalysts like titanium dioxide have the potential to completely mineralize organic compounds in water under ultraviolet light. We are proposing to develop new porous oxide semiconductor materials made up of titanium and niobium mixed oxide nanocomposites. The porous catalysts retain high catalytic activity while being easy to handle and filter out of product streams. New synthetic methods are to be developed that optimize physical properties and the catalyst's ability to photo-degrade organic contaminants in water.

  17. Anodic oxidation of titanium: from technical aspects to biomedical applications.

    PubMed

    Diamanti, Maria Vittoria; Del Curto, Barbara; Pedeferri, Mariapia

    2011-01-01

    Titanium biomaterials are widely employed to produce medical components, such as hip and knee-joint prostheses, bone plates and screws, dental implants, pacemaker cases, surgical equipment, etc. Their diffusion is ascribed to the broad spectrum of optimal mechanical and surface properties, such as the corrosion resistance and correlated low ionic release, the biocompatibility, and especially, the enhanced osseointegration that can be achieved by surface modifications, particularly by suitable anodizing treatments. This review is intended to provide a survey of the wide class of anodic oxidation treatments on titanium, focusing on the oxide structures, morphologies, and compositions that best apply to the variegated fields of titanium applications. PMID:21607937

  18. Review on anode material development in solid oxide fuel cells

    NASA Astrophysics Data System (ADS)

    Siong @ Mahmud, Lily; Muchtar, Andanastuti; Somalu, Mahendra Rao

    2015-05-01

    New developments in technology require highly efficient, affordable, and green electrical energy. The materials to be used must also be reusable and environment friendly. These characteristics are among the major factors that may lead to the production of new and highly efficient power generation systems. Solid oxide fuel cells (SOFCs) have become major devices in producing electricity that emphasize the advance usage of material science and technological development. As part of the key elements of SOFCs, anodes have the primary function of stimulating the electrochemical oxidation of fuel. In this review, the progress in developing anode materials for SOFCs is briefly discussed.

  19. Lithium ion battery application of porous composite oxide microcubes prepared via metal-organic frameworks

    NASA Astrophysics Data System (ADS)

    Yang, Xia; Tang, Yong-Bing; Huang, Xing; Xue, Hong Tao; Kang, Wen Pei; Li, Wen Yue; Ng, Tsz-Wai; Lee, Chun-Sing

    2015-06-01

    Prussian Blue (PB, Fe4[Fe(CN)6]3) is utilized to synthesize bimetallic metal-organic frameworks (MOFs) (Fe4[Fe(CN)6]3/Mx[Fe(CN)6], M = Cu, Ni, Co, etc.) by cation exchange, driven by differences in solubility product constant (Ksp) of monometallic MOFs. Upon decomposition, the bimetallic MOFs convert to porous composite metal oxides (Fe2O3/MOx, M = Cu, Ni, Co, etc.) while keeping the original cubic morphology. This study demonstrates a general approach for preparing bimetallic MOFs and porous composite oxides. We also demonstrate the good electrochemical performance (specific capacity of 774 mAh g-1 after 120 cycles at 500 mA g-1) of the synthesized porous Fe2O3-CuO composite as an anode material for lithium ion batteries. And according to references, this composite exhibit better or comparable rate capability and cycle stability compared with other hybrid transition metal oxides.

  20. An alternative route for the synthesis of silicon nanowires via porous anodic alumina masks

    PubMed Central

    2011-01-01

    Amorphous Si nanowires have been directly synthesized by a thermal processing of Si substrates. This method involves the deposition of an anodic aluminum oxide mask on a crystalline Si (100) substrate. Fe, Au, and Pt thin films with thicknesses of ca. 30 nm deposited on the anodic aluminum oxide-Si substrates have been used as catalysts. During the thermal treatment of the samples, thin films of the metal catalysts are transformed in small nanoparticles incorporated within the pore structure of the anodic aluminum oxide mask, directly in contact with the Si substrate. These homogeneously distributed metal nanoparticles are responsible for the growth of Si nanowires with regular diameter by a simple heating process at 800°C in an Ar-H2 atmosphere and without an additional Si source. The synthesized Si nanowires have been characterized by field emission scanning electron microscopy, high-resolution transmission electron microscopy, X-ray photoelectron spectroscopy, and Raman. PMID:21849077

  1. Outstanding supercapacitive properties of Mn-doped TiO2 micro/nanostructure porous film prepared by anodization method

    NASA Astrophysics Data System (ADS)

    Ning, Xuewen; Wang, Xixin; Yu, Xiaofei; Zhao, Jianling; Wang, Mingli; Li, Haoran; Yang, Yang

    2016-03-01

    Mn-doped TiO2 micro/nanostructure porous film was prepared by anodizing a Ti-Mn alloy. The film annealed at 300 °C yields the highest areal capacitance of 1451.3 mF/cm2 at a current density of 3 mA/cm2 when used as a high-performance supercapacitor electrode. Areal capacitance retention is 63.7% when the current density increases from 3 to 20 mA/cm2, and the capacitance retention is 88.1% after 5,000 cycles. The superior areal capacitance of the porous film is derived from the brush-like metal substrate, which could greatly increase the contact area, improve the charge transport ability at the oxide layer/metal substrate interface, and thereby significantly enhance the electrochemical activities toward high performance energy storage. Additionally, the effects of manganese content and specific surface area of the porous film on the supercapacitive performance were also investigated in this work.

  2. Outstanding supercapacitive properties of Mn-doped TiO2 micro/nanostructure porous film prepared by anodization method.

    PubMed

    Ning, Xuewen; Wang, Xixin; Yu, Xiaofei; Zhao, Jianling; Wang, Mingli; Li, Haoran; Yang, Yang

    2016-01-01

    Mn-doped TiO2 micro/nanostructure porous film was prepared by anodizing a Ti-Mn alloy. The film annealed at 300 °C yields the highest areal capacitance of 1451.3 mF/cm(2) at a current density of 3 mA/cm(2) when used as a high-performance supercapacitor electrode. Areal capacitance retention is 63.7% when the current density increases from 3 to 20 mA/cm(2), and the capacitance retention is 88.1% after 5,000 cycles. The superior areal capacitance of the porous film is derived from the brush-like metal substrate, which could greatly increase the contact area, improve the charge transport ability at the oxide layer/metal substrate interface, and thereby significantly enhance the electrochemical activities toward high performance energy storage. Additionally, the effects of manganese content and specific surface area of the porous film on the supercapacitive performance were also investigated in this work. PMID:26940546

  3. Non-aqueous electrodeposition of porous tin-based film as an anode for lithium-ion battery

    NASA Astrophysics Data System (ADS)

    Gu, C. D.; Mai, Y. J.; Zhou, J. P.; You, Y. H.; Tu, J. P.

    2012-09-01

    Porous tin-based films are electrodeposited on copper foils from a choline chloride/ethylene glycol based electrolyte containing SnCl2·2H2O without any complexing agent or additive. Increasing the deposition time and voltage produces thicker films. The initially deposited Sn grains are relatively uniform with an average size of 200-300 nm and a kind of self-assembly distribution constructing an open and bicontinuous porous network. The architecture of these films possesses a double-layer structure, i.e. SnO2 (superficial layer)/Sn-Cu alloy (bottom layer), which is revealed by X-ray diffractometer and X-ray photoelectron spectroscopy. The electrochemical performance of the porous tin-based films as anode for lithium-ion batteries is measured. Although the capacity fades gradually with repeated cycling, a reversible capacity of 300-350 mAh g-1 is maintained for more than 50 cycles, which suggests that the in situ formed Sn--Cu alloy could provide an interlocking interface between active materials and current collector. Therefore, the tin's shedding from the current collector can be restrained. Moreover, the inactive materials, such as the oxide in the superficial layer and the Cu in the bottom layer, could also act as buffers to relieve the induced volume expansion of Sn during the repeated lithiathion/delithiation process, thus giving the good cycle performances.

  4. Outstanding supercapacitive properties of Mn-doped TiO2 micro/nanostructure porous film prepared by anodization method

    PubMed Central

    Ning, Xuewen; Wang, Xixin; Yu, Xiaofei; Zhao, Jianling; Wang, Mingli; Li, Haoran; Yang, Yang

    2016-01-01

    Mn-doped TiO2 micro/nanostructure porous film was prepared by anodizing a Ti-Mn alloy. The film annealed at 300 °C yields the highest areal capacitance of 1451.3 mF/cm2 at a current density of 3 mA/cm2 when used as a high-performance supercapacitor electrode. Areal capacitance retention is 63.7% when the current density increases from 3 to 20 mA/cm2, and the capacitance retention is 88.1% after 5,000 cycles. The superior areal capacitance of the porous film is derived from the brush-like metal substrate, which could greatly increase the contact area, improve the charge transport ability at the oxide layer/metal substrate interface, and thereby significantly enhance the electrochemical activities toward high performance energy storage. Additionally, the effects of manganese content and specific surface area of the porous film on the supercapacitive performance were also investigated in this work. PMID:26940546

  5. The experimental dielectric function of porous anodic alumina in the infrared region; a comparison with the Maxwell-Garnett model

    NASA Astrophysics Data System (ADS)

    Wäckelgård, Ewa

    1996-06-01

    The infrared reflectance from thin alumina films on metal substrates has a deep minimum for p-polarized light at oblique incidence. This originates from absorption when light couples with a longitudinal optical (LO) phonon mode with k-vector zero. The absorption band is wide for amorphous alumina and is shifted to longer wavelengths for porous oxides compared to non-porous ones. Anodic alumina, prepared in phosphoric acid, with a pore volume fraction of 0.3, has been investigated. The s- and p-polarized reflectance has been measured for selected angles of incidence between 0953-8984/8/23/019/img1 and 0953-8984/8/23/019/img2, and the dielectric function has been determined from these measurements. The effective dielectric function has been calculated using Maxwell-Garnett effective-medium theory for a two-component anisotropic medium consisting of air-filled cylindrical pores perpendicular to the surface in an alumina matrix with optical constants of non-porous evaporated alumina. The theoretical and experimental results are in good agreement, which shows that the redshift of the LO mode absorption for p-polarized light can be explained by the presence of pores.

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

    NASA Astrophysics Data System (ADS)

    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

  7. Effect of anodizing voltage on the sorption of water molecules on porous alumina

    NASA Astrophysics Data System (ADS)

    Vrublevsky, I.; Chernyakova, K.; Bund, A.; Ispas, A.; Schmidt, U.

    2012-05-01

    The amount of water adsorbed on different centers on the surface of oxalic acid alumina films is a function of the anodizing voltage. It is decreased with increasing the anodizing voltage from 20 up to 50 V, came up to maximum value at 20-30 V and slightly increased at voltages above 50 V. Water adsorption by oxide films formed at voltages below 50 V can be due to the negative surface charge that is present on the alumina surface. The negative surface charge disappears in the films formed at voltages higher than 50 V, and thus, the water is adsorbed on aluminum ions in a tetrahedral and octahedral environment. The correlation between anodizing conditions of aluminum in oxalic acid and the structure and composition of anodic alumina was established by Fourier transform infrared spectroscopy (FTIR) and scanning electron microscopy (SEM), thermogravimetric and differential thermal analyses (TG/DTA).

  8. Fabrication of canonical nanoporous templates by variational anodic oxidation of aluminum

    NASA Astrophysics Data System (ADS)

    Chowdhury, Ataur; Wallace, Patrick

    2013-03-01

    The interesting effects of quantum confinement critically depend on the shape and size of the nanocrystals. Preliminary results of an experimental study of production of templates with conical profiles are presented here. These templates will be ideal for fabrication of nanocrytals with the same profile. Templates were fabricated in aluminum with the anodic oxidation process by carefully controlling the anodization parameters to control the shape of the resulting templates. Different combinations of theses parameters such as electrolyte, pH of the solution, applied voltage, and current density were studied to ascertain the right condition of growth for conically porous templates. The most dominant parameter was the applied voltage and the voltage was continuously changed slowly during the process of growth. Attempt was made to control the pore diameter to a size less than 20 nm with an aspect ratio of about 1.0. Structural and morphological studies were done with AFM and SEM. The details of the results will be presented.

  9. Adsorption on ordered and disordered duplex layers of porous anodic alumina.

    PubMed

    Bruschi, Lorenzo; Mistura, Giampaolo; Phadungbut, Poomiwat; Do, D D; Nicholson, D; Mayamei, Yashar; Lee, Woo

    2015-05-01

    We have carried out systematic experiments and numerical simulations of the adsorption on porous anodic aluminum oxide (AAO) duplex layers presenting either an ordered or a disordered interconnecting interface between the large (cavity) and small (constriction) sections of the structured pores. Selective blocking of the pore openings resulted in three different pore topologies: open structured pores, funnel pores, and ink-bottle pores. In the case of the structured pores having an ordered interface, the adsorption isotherms present a rich phenomenology characterized by the presence of two steps in the condensation branch and the opening of one (two) hysteresis loops during evaporation for the ink-bottle (open and funnel) pores. The isotherms can be obtained by summing the isotherms measured on uniform pores having the dimensions of the constrictions or of the cavities. The numerical analysis of the three different pore topologies indicates that the shape of the junction between the two pore sections is only important for the adsorption branch. In particular, a conic junction which resembles that of the AAO pores represents the experimental isotherms for the open and funnel pores better, but the shape of the junction in the ink bottle pores does not matter. The isotherms for the duplex layers with a disordered interface display the same general features found for the ordered duplex layers. In both cases, the adsorption branches coincide and have two steps which are shifted to lower relative pressures compared to those for the ordered duplex. Furthermore, the desorption branches comprise hysteresis loops much wider than those of the ordered duplex layers. Overall, this study highlights the important role played by morphologies where there are interconnections between large and small pores. PMID:25871845

  10. Highly regular anatase nanotubule arrays fabricated in porous anodic templates

    NASA Astrophysics Data System (ADS)

    Michailowski, Alexej; AlMawlawi, Diyaa; Cheng, Guosheng; Moskovits, Martin

    2001-11-01

    Compact, continuous and uniform anatase nanotubules with diameters in the range 50-70 nm were produced inside PAO nano-templates by pressure impregnating the PAO pores with titanium isopropoxide then oxidatively decomposing the reagent at 500 °C. Cleaning the surface of the template and repeating the process several times produced titania nanotubules with a wall thickness ˜3 nm per impregnation. The tube exteriors appeared to be faithful replicas of the pores in which they were formed. The crystallinity and form (anatase) of the titania were determined using XRD and Raman spectroscopy. Tubules in this low diameter range could not be produced using sol-gel.

  11. Solid oxide fuel cells having porous cathodes infiltrated with oxygen-reducing catalysts

    SciTech Connect

    Liu, Meilin; Liu, Ze; Liu, Mingfei; Nie, Lifang; Mebane, David Spencer; Wilson, Lane Curtis; Surdoval, Wayne

    2014-08-12

    Solid-oxide fuel cells include an electrolyte and an anode electrically coupled to a first surface of the electrolyte. A cathode is provided, which is electrically coupled to a second surface of the electrolyte. The cathode includes a porous backbone having a porosity in a range from about 20% to about 70%. The porous backbone contains a mixed ionic-electronic conductor (MIEC) of a first material infiltrated with an oxygen-reducing catalyst of a second material different from the first material.

  12. High-speed growth and photoluminescence of porous anodic alumina films with controllable interpore distances over a large range

    NASA Astrophysics Data System (ADS)

    Li, Y. B.; Zheng, M. J.; Ma, L.

    2007-08-01

    Highly ordered porous anodic alumina (PAA) films are fabricated with high efficiency by stable high-field anodization in oxalic acid/ethanol/water electrolytes at 100-180V and sulfuric acid/oxalic acid/ethanol/water electrolytes at 30-80V, giving interpore distances in the range of 225-450nm and 70-140nm, respectively. The photoluminescence of PAA films prepared by high-field anodization shows remarkable redshift of the peak position and decrease of the intensity compared to that of PAA films formed by conventional low-field anodization.

  13. Monodisperse Porous Silicon Spheres as Anode Materials for Lithium Ion Batteries

    NASA Astrophysics Data System (ADS)

    Wang, Wei; Favors, Zachary; Ionescu, Robert; Ye, Rachel; Bay, Hamed Hosseini; Ozkan, Mihrimah; Ozkan, Cengiz S.

    2015-03-01

    Highly monodisperse porous silicon nanospheres (MPSSs) are synthesized via a simple and scalable hydrolysis process with subsequent surface-protected magnesiothermic reduction. The spherical nature of the MPSSs allows for a homogenous stress-strain distribution within the structure during lithiation and delithiation, which dramatically improves the electrochemical stability. To fully extract the real performance of the MPSSs, carbon nanotubes (CNTs) were added to enhance the electronic conductivity within the composite electrode structure, which has been verified to be an effective way to improve the rate and cycling performance of anodes based on nano-Si. The Li-ion battery (LIB) anodes based on MPSSs demonstrate a high reversible capacity of 3105 mAh g-1. In particular, reversible Li storage capacities above 1500 mAh g-1 were maintained after 500 cycles at a high rate of C/2. We believe this innovative approach for synthesizing porous Si-based LIB anode materials by using surface-protected magnesiothermic reduction can be readily applied to other types of SiOx nano/microstructures.

  14. Monodisperse porous silicon spheres as anode materials for lithium ion batteries.

    PubMed

    Wang, Wei; Favors, Zachary; Ionescu, Robert; Ye, Rachel; Bay, Hamed Hosseini; Ozkan, Mihrimah; Ozkan, Cengiz S

    2015-01-01

    Highly monodisperse porous silicon nanospheres (MPSSs) are synthesized via a simple and scalable hydrolysis process with subsequent surface-protected magnesiothermic reduction. The spherical nature of the MPSSs allows for a homogenous stress-strain distribution within the structure during lithiation and delithiation, which dramatically improves the electrochemical stability. To fully extract the real performance of the MPSSs, carbon nanotubes (CNTs) were added to enhance the electronic conductivity within the composite electrode structure, which has been verified to be an effective way to improve the rate and cycling performance of anodes based on nano-Si. The Li-ion battery (LIB) anodes based on MPSSs demonstrate a high reversible capacity of 3105 mAh g(-1). In particular, reversible Li storage capacities above 1500 mAh g(-1) were maintained after 500 cycles at a high rate of C/2. We believe this innovative approach for synthesizing porous Si-based LIB anode materials by using surface-protected magnesiothermic reduction can be readily applied to other types of SiOx nano/microstructures. PMID:25740298

  15. Monodisperse Porous Silicon Spheres as Anode Materials for Lithium Ion Batteries

    PubMed Central

    Wang, Wei; Favors, Zachary; Ionescu, Robert; Ye, Rachel; Bay, Hamed Hosseini; Ozkan, Mihrimah; Ozkan, Cengiz S.

    2015-01-01

    Highly monodisperse porous silicon nanospheres (MPSSs) are synthesized via a simple and scalable hydrolysis process with subsequent surface-protected magnesiothermic reduction. The spherical nature of the MPSSs allows for a homogenous stress-strain distribution within the structure during lithiation and delithiation, which dramatically improves the electrochemical stability. To fully extract the real performance of the MPSSs, carbon nanotubes (CNTs) were added to enhance the electronic conductivity within the composite electrode structure, which has been verified to be an effective way to improve the rate and cycling performance of anodes based on nano-Si. The Li-ion battery (LIB) anodes based on MPSSs demonstrate a high reversible capacity of 3105 mAh g−1. In particular, reversible Li storage capacities above 1500 mAh g−1 were maintained after 500 cycles at a high rate of C/2. We believe this innovative approach for synthesizing porous Si-based LIB anode materials by using surface-protected magnesiothermic reduction can be readily applied to other types of SiOx nano/microstructures. PMID:25740298

  16. Three-dimensional porous carbon nanotube sponges for high-performance anodes of microbial fuel cells

    NASA Astrophysics Data System (ADS)

    Erbay, Celal; Yang, Gang; de Figueiredo, Paul; Sadr, Reza; Yu, Choongho; Han, Arum

    2015-12-01

    Highly-porous, light-weight, and inexpensive three-dimensional (3D) sponges consisting of interconnected carbon nanotubes (CNTs) without base materials are synthesized with a facile and scalable one-step chemical vapor deposition process as anode of microbial fuel cells (MFCs). The MFCs generates higher power densities of 2150 W m-3 (per anode volume) or 170 W m-3 (per anode chamber volume), comparable to those of commercial 3D carbon felt electrodes under the same conditions. The high performances are due to excellent charge transfer between CNTs and microbes owing to 13 times lower charge transfer resistance compared to that of carbon felt. The material cost of producing these CNT sponge estimates to be ∼0.1/gCNT, significantly lower than that of other methods. In addition, the high production rate of about 3.6 g h-1 compared to typical production rate of 0.02 g h-1 of other CNT-based materials makes this process economically viable. The one-step synthesis method allowing self-assembly of 3D CNT sponges as they grow is low cost and scalable, making this a promising method for manufacturing high-performance anodes of MFCs, with broad applicability to microbial electrochemical systems in general.

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

    NASA Astrophysics Data System (ADS)

    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.

  18. Vertical single- and double-walled carbon nanotubes grown from modified porous anodic alumina templates

    NASA Astrophysics Data System (ADS)

    Maschmann, Matthew R.; Franklin, Aaron D.; Amama, Placidus B.; Zakharov, Dmitri N.; Stach, Eric A.; Sands, Timothy D.; Fisher, Timothy S.

    2006-08-01

    Vertical single-walled and double-walled carbon nanotube (SWNT and DWNT) arrays have been grown using a catalyst embedded within the pore walls of a porous anodic alumina (PAA) template. The initial film structure consisted of a SiOx adhesion layer, a Ti layer, a bottom Al layer, a Fe layer, and a top Al layer deposited on a Si wafer. The Al and Fe layers were subsequently anodized to create a vertically oriented pore structure through the film stack. CNTs were synthesized from the catalyst layer by plasma-enhanced chemical vapour deposition (PECVD). The resulting structure is expected to form the basis for development of vertically oriented CNT-based electronics and sensors.

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

    NASA Astrophysics Data System (ADS)

    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

  20. Fabrication of Crystalline Indium Tin Oxide Nanobasket Electrodes using Aluminum Anodic Oxide Template

    NASA Astrophysics Data System (ADS)

    Wang, Gou-Jen; Chen, He-Tsing; Yang, Hsihang

    2008-07-01

    Fabrication of crystalline indium tin oxide (ITO) nanobasket electrodes shaped by an anodic aluminum oxide (AAO) template for better electron conductivity is presented. ITO films were deposited on porous AAO templates by RF magnetron sputtering. The sputter-coated ITO films were characterized by field-emission scanning electron microscopy (FESEM) to illustrate the nanobasket morphologies. The compositions of the ITO films were characterized by energy-dispersive X-ray (EDS) analysis. X-ray diffraction (XRD) analysis was conducted to evaluate the crystallinity. The crystallinity can be enhanced by annealing at 300 °C. Although the conductivity of the ITO nanobasket film is larger than that of the conventional ITO thin film, the harvest efficiency can be markedly increased due to the nanobasket structure which enables most of the photoexcited electrons to reach their nearest electrode before losing their momentum. The presented ITO nanobasket films can be further used as a more effective electrode material for photovoltaics such as dye-sensitized solar cells (DSSCs).

  1. Synthesis of nanoporous activated iridium oxide films by anodized aluminum oxide templated atomic layer deposition.

    SciTech Connect

    Comstock, D. J.; Christensen, S. T.; Elam, J. W.; Pellin, M. J.; Hersam, M. C.

    2010-08-01

    Iridium oxide (IrOx) has been widely studied due to its applications in electrochromic devices, pH sensing, and neural stimulation. Previous work has demonstrated that both Ir and IrOx films with porous morphologies prepared by sputtering exhibit significantly enhanced charge storage capacities. However, sputtering provides only limited control over film porosity. In this work, we demonstrate an alternative scheme for synthesizing nanoporous Ir and activated IrOx films (AIROFs). This scheme utilizes atomic layer deposition to deposit a thin conformal Ir film within a nanoporous anodized aluminum oxide template. The Ir film is then activated by potential cycling in 0.1 M H{sub 2}SO{sub 4} to form a nanoporous AIROF. The morphologies and electrochemical properties of the films are characterized by scanning electron microscopy and cyclic voltammetry, respectively. The resulting nanoporous AIROFs exhibit a nanoporous morphology and enhanced cathodal charge storage capacities as large as 311 mC/cm{sup 2}.

  2. Luminescence of Terbium and Neodymium Ions in Yttrium Aluminum Garnet Xerogels on Porous Anodic Alumina

    NASA Astrophysics Data System (ADS)

    Rudenko, M. V.; Gaponenko, N. V.; Mudryi, A. V.; Orekhovskaya, T. I.

    2016-03-01

    Luminescent structures of yttrium aluminum garnet doped with rare-earth elements Tb and Nd (YAG:Tb3+ and YAG:Nd3+) were formed by the sol-gel route on films of porous anodic alumina. The morphology, phase composition, and luminescence of the fabricated structures were investigated. Photoluminescence spectra of the YAG:Tb3+ and YAG:Nd3+ structures revealed emission bands due to electronic transitions of the relevant rare-earth elements. Fine structure was observed in the luminescence bands of all fabricated samples and was associated with the manifestation of a Stark effect.

  3. Collimated microfiber spectroscopy for optical characterization of disordered porous anodic alumina

    NASA Astrophysics Data System (ADS)

    Yoneda, Satoshi; Kimura, Saho; Yamaguchi, Akira; Kimura, Daiki; Ohkoshi, Yutaka; Yamanaka, Shigeru; Usami, Hisanao

    2016-02-01

    A novel collimated microfiber spectroscopy technique using an optical fiber probe with microball lens was developed to observe the photonic crystalline characteristics of porous anodized alumina (PAA) slabs with disordered arrays of holes. Transmittance spectra of the PAA slab observed by the microfiber probe with ball lens showed a broad valley at ∼410 nm; conversely, no significant valley was observed by an ordinary microfiber spectroscope without ball lens. The broad valley was comparable with that observed in a spectrum simulated for a model based on a scanning electron microscopy image of the PAA slab by using the finite-difference time-domain method.

  4. Organic solar cells on indium tin oxide and aluminum doped zinc oxide anodes

    NASA Astrophysics Data System (ADS)

    Schulze, Kerstin; Maennig, Bert; Leo, Karl; Tomita, Yuto; May, Christian; Hüpkes, Jürgen; Brier, Eduard; Reinold, Egon; Bäuerle, Peter

    2007-08-01

    The authors compare organic solar cells using two different transparent conductive oxides as anode: indium tin oxide (ITO) and three kinds of aluminum doped zinc oxide (ZAO). These anodes with different work functions are used for small molecule photovoltaic devices based on an oligothiophene derivative as donor and fullerene C60 as acceptor molecule. It turns out that cells on ITO and ZAO have virtually identical properties. In particular, the authors demonstrate that the work function of the anode does not influence the Voc of the photovoltaic device due to the use of doped transport layers.

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

    PubMed

    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

  6. Designed construction and validation of carbon-free porous MnO spheres with hybrid architecture as anodes for lithium-ion batteries.

    PubMed

    Remith, Pongilat; Kalaiselvi, Nallathamby

    2016-06-21

    Porous micro/nanostructures of earth abundant and ecobenign metals are emerging as advanced green materials for use in electrochemical energy storage devices. We present here the custom designed construction of a hybrid architecture containing porous MnO microspheres, formed out of hierarchically assembled nanoparticles using a template-free co-precipitation method, wherein the sacrificial template growth of porous spheres has been obtained by a solution mediated and time dependent oxidation strategy. The nanoporous channels in the MnO microspheres and the nanosized primary particles of MnO anodes in synergy increase the electrolyte percolation, resulting in a discharge capacity of 1200 mA h g(-1) at a current density of 50 mA g(-1) and a capacity as high as 450 mA h g(-1) under the 1000 mA g(-1) condition. The study assumes importance based on the fact that engineering of electrode materials is typically challenging, wherein design, preparation and fabrication of tailor-made electrodes with a desirable micro/nanocrystalline assembly play a critical role, especially when recommended for high capacity and high-rate applications in electrochemical energy storage devices. Further, this communication elaborates the designed construction and validation of porous MnO microspheres engineered through a time dependent process protocol as economically viable and environmentally benign anodes for lithium-ion batteries. PMID:27233053

  7. Effect of Sulfuric Acid Concentration on Electrochemical Characteristics of Nano Porous Structure Formed by Anodizing Process.

    PubMed

    Lee, Jung-Hyung; Lee, Seung-Jun; Kim, Seong-Jong

    2016-02-01

    Aluminum alloy is a very strong reactivity material, but it has excellent corrosion resistance due to protective oxide film created in air. However, it is not practical because the film thickness is uneven and varies depending on the generation condition. Therefore, aluminum anodizing was performed to form film with commercially applicable hardness, corrosion resistance, and wear resistance. This offers such advantages as commercial applicability to large areas and low prices. In this study, the electrochemical characteristics with concentration of sulfuric acid electrolyte were compared with the two-step anodizing method which is widely used. A surface observation revealed regular structures and pores with the size of several tens of nm, and the anodized film presented excellent corrosion resistance with considerably low corrosion current density in sea water. PMID:27433656

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

    NASA Astrophysics Data System (ADS)

    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. 3D Non-destructive morphological analysis of a solid oxide fuel cell anode using full-field X-ray nano-tomography

    NASA Astrophysics Data System (ADS)

    Karen Chen-Wiegart, Yu-chen; Cronin, J. Scott; Yuan, Qingxi; Yakal-Kremski, Kyle J.; Barnett, Scott A.; Wang, Jun

    2012-11-01

    An accurate 3D morphological analysis is critically needed to study the process-structure-property relationship in many application fields such as battery electrodes, fuel cells and porous materials for sensing and actuating. Here we present the application of a newly developed full field X-ray nano-scale transmission microscopy (TXM) imaging for a non-destructive, comprehensive 3D morphology analysis of a porous Ni-YSZ solid oxide fuel cell anode. A unique combination of improved 3D resolution and large analyzed volume (˜3600 μm3) yields structural data with excellent statistical accuracy. 3D morphological parameters quantified include phase volume fractions, surface and interfacial area densities, phase size distribution, directional connectivity, tortuosity, and electrochemically active triple phase boundary density. A prediction of electrochemical anode polarization resistance based on this microstructural data yielded good agreement with a measured anode resistance via electrochemical impedance spectroscopy. The Mclachlan model is used to estimate the anode electrical conductivity.

  10. X-Ray-, Cathodo-, and Photoluminescence of Yttrium-Aluminum Composites on Porous Anodic Alumina Films

    NASA Astrophysics Data System (ADS)

    Khoroshko, L. S.; Kortov, V. S.; Gaponenko, N. V.; Raichyonok, T. F.; Tikhomirov, S. A.; Pustovarov, V. A.

    2016-07-01

    Yttrium-aluminum composites doped with terbium were synthesized by precipitation on porous anodic alumina fi lms grown on silicon substrates. The fabricated structures demonstrated x-ray-, cathodo-, and photoluminescence with characteristic bands of trivalent terbium upon excitation by Cu Kα x-rays of energy 8.86 keV, a 180-keV electron beam, and optical UV radiation, respectively. The terbium luminescence bands increased in intensity as the terbium concentration increased from 0.01 to 0.25 mol%. The intensity of a broad band in the blue spectral region with a maximum at 410 nm that was due to photoluminescence of the porous anodic alumina fi lm increased as the excitation wavelength increased from 260 to 340 nm. Simultaneously, the intensities of luminescence bands in the range 480-650 nm associated with Tb 3 + 5 D 4 - 7 F j ( j = 3, 4, 5, 6) transitions decreased. The possibility of practical application of the synthesized luminescent structures was discussed.

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

    PubMed

    Vera, María Laura; Rosenberger, Mario Roberto; Schvezov, Carlos Enrique; Ares, Alicia Esther

    2015-01-01

    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. PMID:25784939

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

    PubMed Central

    Schvezov, Carlos Enrique; Ares, Alicia Esther

    2015-01-01

    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. PMID:25784939

  13. Electrocatalyst for alcohol oxidation at fuel cell anodes

    DOEpatents

    Adzic, Radoslav; Kowal, Andrzej

    2011-11-02

    In some embodiments a ternary electrocatalyst is provided. The electrocatalyst can be used in an anode for oxidizing alcohol in a fuel cell. In some embodiments, the ternary electrocatalyst may include a noble metal particle having a surface decorated with clusters of SnO.sub.2 and Rh. The noble metal particles may include platinum, palladium, ruthenium, iridium, gold, and combinations thereof. In some embodiments, the ternary electrocatalyst includes SnO.sub.2 particles having a surface decorated with clusters of a noble metal and Rh. Some ternary electrocatalysts include noble metal particles with clusters of SnO.sub.2 and Rh at their surfaces. In some embodiments the electrocatalyst particle cores are nanoparticles. Some embodiments of the invention provide a fuel cell including an anode incorporating the ternary electrocatalyst. In some aspects a method of using ternary electrocatalysts of Pt, Rh, and SnO.sub.2 to oxidize an alcohol in a fuel cell is described.

  14. Bio-Derived, Binderless, Hierarchically Porous Carbon Anodes for Li-ion Batteries

    NASA Astrophysics Data System (ADS)

    Campbell, Brennan; Ionescu, Robert; Favors, Zachary; Ozkan, Cengiz S.; Ozkan, Mihrimah

    2015-09-01

    Here we explore the electrochemical performance of pyrolyzed skins from the species A. bisporus, also known as the Portobello mushroom, as free-standing, binder-free, and current collector-free Li-ion battery anodes. At temperatures above 900 °C, the biomass-derived carbon nanoribbon-like architectures undergo unique processes to become hierarchically porous. During heat-treatment, the oxygen and heteroatom-rich organics and potassium compounds naturally present in the mushroom skins play a mutual role in creating inner void spaces throughout the resulting carbon nanoribbons, which is a process analogous to KOH-activation of carbon materials seen in literature. The pores formed in the pyrolytic carbon nanoribbons range in size from sub-nanometer to tens of nanometers, making the nanoribbons micro, meso, and macroporous. Detailed studies were conducted on the carbon nanoribbons using SEM and TEM to study morphology, as well as XRD and EDS to study composition. The self-supporting nanoribbon anodes demonstrate significant capacity increase as they undergo additional charge/discharge cycles. After a pyrolysis temperature of 1100 °C, the pristine anodes achieve over 260 mAh/g after 700 cycles and a Coulombic efficiency of 101.1%, without the use of harmful solvents or chemical activation agents.

  15. Bio-Derived, Binderless, Hierarchically Porous Carbon Anodes for Li-ion Batteries

    PubMed Central

    Campbell, Brennan; Ionescu, Robert; Favors, Zachary; Ozkan, Cengiz S.; Ozkan, Mihrimah

    2015-01-01

    Here we explore the electrochemical performance of pyrolyzed skins from the species A. bisporus, also known as the Portobello mushroom, as free-standing, binder-free, and current collector-free Li-ion battery anodes. At temperatures above 900 °C, the biomass-derived carbon nanoribbon-like architectures undergo unique processes to become hierarchically porous. During heat-treatment, the oxygen and heteroatom-rich organics and potassium compounds naturally present in the mushroom skins play a mutual role in creating inner void spaces throughout the resulting carbon nanoribbons, which is a process analogous to KOH-activation of carbon materials seen in literature. The pores formed in the pyrolytic carbon nanoribbons range in size from sub-nanometer to tens of nanometers, making the nanoribbons micro, meso, and macroporous. Detailed studies were conducted on the carbon nanoribbons using SEM and TEM to study morphology, as well as XRD and EDS to study composition. The self-supporting nanoribbon anodes demonstrate significant capacity increase as they undergo additional charge/discharge cycles. After a pyrolysis temperature of 1100 °C, the pristine anodes achieve over 260 mAh/g after 700 cycles and a Coulombic efficiency of 101.1%, without the use of harmful solvents or chemical activation agents. PMID:26415917

  16. Bio-Derived, Binderless, Hierarchically Porous Carbon Anodes for Li-ion Batteries.

    PubMed

    Campbell, Brennan; Ionescu, Robert; Favors, Zachary; Ozkan, Cengiz S; Ozkan, Mihrimah

    2015-01-01

    Here we explore the electrochemical performance of pyrolyzed skins from the species A. bisporus, also known as the Portobello mushroom, as free-standing, binder-free, and current collector-free Li-ion battery anodes. At temperatures above 900 °C, the biomass-derived carbon nanoribbon-like architectures undergo unique processes to become hierarchically porous. During heat-treatment, the oxygen and heteroatom-rich organics and potassium compounds naturally present in the mushroom skins play a mutual role in creating inner void spaces throughout the resulting carbon nanoribbons, which is a process analogous to KOH-activation of carbon materials seen in literature. The pores formed in the pyrolytic carbon nanoribbons range in size from sub-nanometer to tens of nanometers, making the nanoribbons micro, meso, and macroporous. Detailed studies were conducted on the carbon nanoribbons using SEM and TEM to study morphology, as well as XRD and EDS to study composition. The self-supporting nanoribbon anodes demonstrate significant capacity increase as they undergo additional charge/discharge cycles. After a pyrolysis temperature of 1100 °C, the pristine anodes achieve over 260 mAh/g after 700 cycles and a Coulombic efficiency of 101.1%, without the use of harmful solvents or chemical activation agents. PMID:26415917

  17. Tin nanoparticle-loaded porous carbon nanofiber composite anodes for high current lithium-ion batteries

    NASA Astrophysics Data System (ADS)

    Shen, Zhen; Hu, Yi; Chen, Yanli; Zhang, Xiangwu; Wang, Kehao; Chen, Renzhong

    2015-03-01

    Metallic Sn is a promising high-capacity anode material for use in lithium-ion batteries (LIBs), but its huge volume variation during lithium ion insertion/extraction typically results in poor cycling stability. To address this, we demonstrate the fabrication of Sn nanoparticle-loaded porous carbon nanofiber (Sn-PCNF) composites via the electrospinning of Sn(II) acetate/mineral oil/polyacrylonitrile precursors in N,N-dimethylformamide solvent and their subsequent carbonization at 700 °C under an argon atmosphere. This is shown to result in an even distribution of pores on the surface of the nanofibers, allowing the Sn-PCNF composite to be used directly as an anode in lithium-ion batteries without the need to add non-active materials such as polymer binders or electrical conductors. With a discharge capacity of around 774 mA h g-1 achieved at a high current of 0.8 A g-1 over 200 cycles, this material clearly has a high rate capability and excellent cyclic stability, and thanks to its unique structure and properties, is an excellent candidate for use as an anode material in high-current rechargeable lithium-ion batteries.

  18. Novel light-weight, high-performance anode-supported microtubular solid oxide fuel cells with an active anode functional layer

    NASA Astrophysics Data System (ADS)

    Liu, Tong; Wang, Yao; Ren, Cong; Fang, Shumin; Mao, Yating; Chen, Fanglin

    2015-10-01

    Influence of the air-gap, the distance from the tube-in-orifice spinneret to the upper surface of the external coagulant bath during the extrusion/phase-inversion process, on the microstructure of nickel - yttria-stabilized zirconia (Ni-YSZ) hollow fibers has been systematically studied. When the air-gap is 0 cm, the obtained Ni-YSZ hollow fiber has a sandwich microstructure. However, when the air-gap is increased to 15 cm, a bi-layer Ni-YSZ hollow fiber consisting of a thin layer with small pores and a thick support with highly porous fingerlike macrovoids has been achieved. The output power density of microtubular solid oxide fuel cells (MT-SOFCs) with a cell configuration of Ni-YSZ/YSZ/YSZ-LSM increases from 594 mW cm-2 for the cells with the Ni-YSZ anode of sandwich microstructure to 832 mW cm-2 for the cells with the Ni-YSZ anode of bi-layer microstructure at 750 °C, implying that to achieve the same output power density, the weight of the cells with the bi-layer anode support can be reduced to 41.5% compared with that of the cells with the sandwich anode support. Thermal-cycling test shows no obvious degradation on the open-circuit-voltage (OCV), indicating that the MT-SOFCs have robust resistance to thermal cycling.

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

    NASA Astrophysics Data System (ADS)

    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.

  20. Synthesis and characterization of anodized titanium-oxide nanotube arrays

    SciTech Connect

    Hu, Michael Z.; Lai, Peng; Bhuiyan, Md S; Tsouris, Costas; Gu, Baohua; Paranthaman, Mariappan Parans; Gabitto, Jorge; Harrison, L. D.

    2009-01-01

    Anodized titanium-oxide containing highly ordered, vertically oriented TiO2 nanotube arrays is a nanomaterial architecture that shows promise for diverse applications. In this paper, an anodization synthesis using HF-free aqueous solution is described. The anodized TiO2 film samples (amorphous, anatase, and rutile) on titanium foils were characterized with scanning electron microscopy, X-ray diffraction, and Raman spectroscopy. Additional characterization in terms of photocurrent generated by an anode consisting of a titanium foil coated by TiO2 nanotubes was performed using an electrochemical cell. A platinum cathode was used in the electrochemical cell. Results were analyzed in terms of the efficiency of the current generated, defined as the ratio of the difference between the electrical energy output and the electrical energy input divided by the input radiation energy, with the goal of determining which phase of TiO2 nanotubes leads to more efficient hydrogen production. It was determined that the anatase crystalline structure converts light into current more efficiently and is therefore a better photocatalytic material for hydrogen production via photoelectrochemical splitting of water.

  1. Chemical compatibility and properties of suspension plasma-sprayed SrTiO3-based anodes for intermediate-temperature solid oxide fuel cells

    NASA Astrophysics Data System (ADS)

    Zhang, Shan-Lin; Li, Cheng-Xin; Li, Chang-Jiu

    2014-10-01

    La-doped strontium titanate (LST) is a promising, redox-stable perovskite material for direct hydrocarbon oxidation anodes in intermediate-temperature solid oxide fuel cells (IT-SOFCs). In this study, nano-sized LST and Sm-doped ceria (SDC) powders are produced by the sol-gel and glycine-nitrate processes, respectively. The chemical compatibility between LST and electrolyte materials is studied. A LST-SDC composite anode is prepared by suspension plasma spraying (SPS). The effects of annealing conditions on the phase structure, microstructure, and chemical stability of the LST-SDC composite anode are investigated. The results indicate that the suspension plasma-sprayed LST-SDC anode has the same phase structure as the original powders. LST exhibits a good chemical compatibility with SDC and Mg/Sr-doped lanthanum gallate (LSGM). The anode has a porosity of ∼40% with a finely porous structure that provides high gas permeability and a long three-phase boundary for the anode reaction. Single cells assembled with the LST-SDC anode, La0.8Sr0.2Ga0.8Mg0.2O3 electrolyte, and La0.8Sr0.2CoO3-SDC cathode show a good performance at 650-800 °C. The annealing reduces the impedances due to the enhancement in the bonding between the particles in the anode and interface of anode and LSGM electrolyte, thus improving the output performance of the cell.

  2. LOW-TEMPERATURE, ANODE-SUPPORTED HIGH POWER DENSITY SOLID OXIDE FUEL CELLS WITH NANOSTRUCTURED ELECTRODES

    SciTech Connect

    Anil V. Virkar

    2001-09-26

    Anode-supported solid oxide fuel cells with Ni + yttria-stabilized zirconia (YSZ) anode, YSZ-samaria-doped ceria (SDC) bi-layer electrolyte and Sr-doped LaCoO{sub 3} (LSC) + SDC cathode were fabricated. Fuel used consisted of H{sub 2} diluted with He, N{sub 2}, H{sub 2}O or CO{sub 2}, mixtures of H{sub 2} and CO, and mixtures of CO and CO{sub 2}. Cell performance was measured at 800 C with above-mentioned fuel gas mixtures and air as oxidant. For a given concentration of the diluent, the cell performance was higher with He as the diluent than with N{sub 2} as the diluent. Mass transport through porous Ni-YSZ anode for H{sub 2}-H{sub 2}O, CO-CO{sub 2} binary systems and H{sub 2}-H{sub 2}O-diluent gas ternary systems was analyzed using multicomponent gas diffusion theory. At high concentrations of the diluent, the maximum achievable current density was limited by the anodic concentration polarization. From this measured limiting current density, the corresponding effective gas diffusivity was estimated. Highest effective diffusivity was estimated for fuel gas mixtures containing H{sub 2}-H{sub 2}O-He mixtures ({approx}0.34 cm{sup 2}/s), and the lowest for CO-CO{sub 2} mixtures ({approx}0.07 cm{sup 2}/s). The lowest performance was observed with CO-CO{sub 2} mixture as a fuel, which in part was attributed to the lowest effective diffusivity of the fuels tested.

  3. Direct oxidation solid oxide fuel cell: Aspects of anode performance optimization

    NASA Astrophysics Data System (ADS)

    Costa-Nunes, Olga

    I have examined the impact of high fuel utilization and anode catalyst stability for Cu-based anodes in solid oxide fuel cells (SOFC). First, the performance of SOFC with Cu-ceria-YSZ anodes was studied in n-butane at 973 K as a function of fuel conversion. Conversion led to dilution of the fuel which resulted in a significant decrease in performance at higher fuel conversions. I demonstrated that the inclusion of a steam-reforming catalyst within the anode compartment of direct-oxidation SOFC improved performance at high fuel utilization. The performance of a Cu-CeO2-YSZ SOFC was compared to a conventional SOFC with Ni-YSZ anode while operating on H2, CO, and syngas fuels. Cells with Cu-CeO2-YSZ anodes exhibit similar performance when operating on H2 or CO fuels, while cells with Ni-YSZ anodes exhibited substantially lower performance when operating on CO compared to H2. My work demonstrated that dilution of H2 by H2O has little effect on the kinetics of H2 oxidation on both the Cu-CeO 2-YSZ and Ni-YSZ anodes. In addition, I have investigated the thermal stability of the anode catalyst, ceria, was using thin ceria films supported on YSZ. Special attention was given to the interactions between ceria and YSZ under high temperature treatments in reducing and oxidizing environments. My results have shown that ceria films on YSZ are highly mobile at relatively moderate temperatures and their morphology depends on the gas environment to which they have been exposed. Studies with alpha-Al2O3 assisted in clarifying the role of the substrate in the treatment effects on ceria.

  4. Porous Nickel Oxide Film Sensor for Formaldehyde

    NASA Astrophysics Data System (ADS)

    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.

  5. Nitric oxide-releasing porous silicon nanoparticles

    NASA Astrophysics Data System (ADS)

    Kafshgari, Morteza Hasanzadeh; Cavallaro, Alex; Delalat, Bahman; Harding, Frances J.; McInnes, Steven JP; Mäkilä, Ermei; Salonen, Jarno; Vasilev, Krasimir; Voelcker, Nicolas H.

    2014-07-01

    In this study, the ability of porous silicon nanoparticles (PSi NPs) to entrap and deliver nitric oxide (NO) as an effective antibacterial agent is tested against different Gram-positive and Gram-negative bacteria. NO was entrapped inside PSi NPs functionalized by means of the thermal hydrocarbonization (THC) process. Subsequent reduction of nitrite in the presence of d-glucose led to the production of large NO payloads without reducing the biocompatibility of the PSi NPs with mammalian cells. The resulting PSi NPs demonstrated sustained release of NO and showed remarkable antibacterial efficiency and anti-biofilm-forming properties. These results will set the stage to develop antimicrobial nanoparticle formulations for applications in chronic wound treatment.

  6. Nitric oxide-releasing porous silicon nanoparticles

    PubMed Central

    2014-01-01

    In this study, the ability of porous silicon nanoparticles (PSi NPs) to entrap and deliver nitric oxide (NO) as an effective antibacterial agent is tested against different Gram-positive and Gram-negative bacteria. NO was entrapped inside PSi NPs functionalized by means of the thermal hydrocarbonization (THC) process. Subsequent reduction of nitrite in the presence of d-glucose led to the production of large NO payloads without reducing the biocompatibility of the PSi NPs with mammalian cells. The resulting PSi NPs demonstrated sustained release of NO and showed remarkable antibacterial efficiency and anti-biofilm-forming properties. These results will set the stage to develop antimicrobial nanoparticle formulations for applications in chronic wound treatment. PMID:25114633

  7. Structural transformation of nickel hydroxide films during anodic oxidation

    SciTech Connect

    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.

  8. Eutectic Nano-Droplet Template Injection into Bulk Silicon to Construct Porous Frameworks with Concomitant Conformal Coating as Anodes for Li-Ion Batteries

    NASA Astrophysics Data System (ADS)

    Qu, Fei; Li, Chilin; Wang, Zumin; Wen, Yuren; Richter, Gunther; Strunk, Horst P.

    2015-05-01

    Building porosity in monolithic materials is highly desired to design 3D electrodes, however ex-situ introduction or in-situ generation of nano-scale sacrificial template is still a great challenge. Here Al-Si eutectic droplet templates are uniformly injected into bulk Si through Al-induced solid-solid convection to construct a highly porous Si framework. This process is concomitant with process-inherent conformal coating of ion-conductive oxide. Such an all-in-one method has generated a (continuously processed) high-capacity Si anode integrating longevity and stable electrolyte-anode diaphragm for Li-ion batteries (e.g. a reversible capacity as large as ~1800 mAh/g or ~350 μAh/cm2-μm with a CE of ~99% at 0.1 C after long-term 400 cycles).

  9. Eutectic Nano-Droplet Template Injection into Bulk Silicon to Construct Porous Frameworks with Concomitant Conformal Coating as Anodes for Li-Ion Batteries

    PubMed Central

    Qu, Fei; Li, Chilin; Wang, Zumin; Wen, Yuren; Richter, Gunther; Strunk, Horst P.

    2015-01-01

    Building porosity in monolithic materials is highly desired to design 3D electrodes, however ex-situ introduction or in-situ generation of nano-scale sacrificial template is still a great challenge. Here Al-Si eutectic droplet templates are uniformly injected into bulk Si through Al-induced solid-solid convection to construct a highly porous Si framework. This process is concomitant with process-inherent conformal coating of ion-conductive oxide. Such an all-in-one method has generated a (continuously processed) high-capacity Si anode integrating longevity and stable electrolyte-anode diaphragm for Li-ion batteries (e.g. a reversible capacity as large as ~1800 mAh/g or ~350 μAh/cm2-μm with a CE of ~99% at 0.1 C after long-term 400 cycles). PMID:25988370

  10. Eutectic nano-droplet template injection into bulk silicon to construct porous frameworks with concomitant conformal coating as anodes for Li-ion batteries.

    PubMed

    Qu, Fei; Li, Chilin; Wang, Zumin; Wen, Yuren; Richter, Gunther; Strunk, Horst P

    2015-01-01

    Building porosity in monolithic materials is highly desired to design 3D electrodes, however ex-situ introduction or in-situ generation of nano-scale sacrificial template is still a great challenge. Here Al-Si eutectic droplet templates are uniformly injected into bulk Si through Al-induced solid-solid convection to construct a highly porous Si framework. This process is concomitant with process-inherent conformal coating of ion-conductive oxide. Such an all-in-one method has generated a (continuously processed) high-capacity Si anode integrating longevity and stable electrolyte-anode diaphragm for Li-ion batteries (e.g. a reversible capacity as large as ~1800 mAh/g or ~350 μAh/cm(2)-μm with a CE of ~99% at 0.1 C after long-term 400 cycles). PMID:25988370

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

    PubMed

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

    2016-06-01

    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. PMID:27189412

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

    PubMed

    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

  13. LOW-TEMPERATURE, ANODE-SUPPORTED HIGH POWER DENSITY SOLID OXIDE FUEL CELLS WITH NANOSTRUCTURED ELECTRODES

    SciTech Connect

    Professor Anil V. Virkar

    2003-05-23

    This report summarizes the work done during the entire project period, between October 1, 1999 and March 31, 2003, which includes a six-month no-cost extension. During the project, eight research papers have, either been, published, accepted for publication, or submitted for publication. In addition, several presentations have been made in technical meetings and workshops. The project also has provided support for four graduate students working towards advanced degrees. The principal technical objective of the project was to analyze the role of electrode microstructure on solid oxide fuel cell performance. Prior theoretical work conducted in our laboratory demonstrated that the particle size of composite electrodes has a profound effect on cell performance; the finer the particle size, the lower the activation polarization, the better the performance. The composite cathodes examined consisted of electronically conducting perovskites such as Sr-doped LaMnO{sub 3} (LSM) or Sr-doped LaCoO{sub 3} (LSC), which is also a mixed conductor, as the electrocatalyst, and yttria-stabilized zirconia (YSZ) or rare earth oxide doped CeO{sub 2} as the ionic conductor. The composite anodes examined were mixtures of Ni and YSZ. A procedure was developed for the synthesis of nanosize YSZ by molecular decomposition, in which unwanted species were removed by leaching, leaving behind nanosize YSZ. Anode-supported cells were made using the as-synthesized powders, or using commercially acquired powders. The electrolyte was usually a thin ({approx}10 microns), dense layer of YSZ, supported on a thick ({approx}1 mm), porous Ni + YSZ anode. The cathode was a porous mixture of electrocatalyst and an ionic conductor. Most of the cell testing was done at 800 C with hydrogen as fuel and air as the oxidant. Maximum power densities as high as 1.8 W/cm{sup 2} were demonstrated. Polarization behavior of the cells was theoretically analyzed. A limited amount of cell testing was done using liquid

  14. Porous mixed metal oxides: design, formation mechanism, and application in lithium-ion batteries

    NASA Astrophysics Data System (ADS)

    Wu, Fangfang; Bai, Jing; Feng, Jinkui; Xiong, Shenglin

    2015-10-01

    The relentless pursuit of new electrode materials for lithium ion batteries (LIBs) has been conducted for decades. Structures with either porous or nanostructure configurations have been confirmed as advantageous candidates for energy storage/conversion applications. The integration of the two features into one structure can provide another chance to improve the electroactivities. Recently, single-phased mixed metal oxides (MMOs) containing different metal cations, in particular, have confirmed high electrochemical activities because of their complex chemical composition, interfacial effects, and the synergic effects of the multiple metal species. In this review, we will focus on recent research advances of MMOs with porous architectures as anode materials in the matter of structural arrangement and compositional manipulation. Moreover, the application of self-supported MMO-based porous structures as LIB anodes is also explained herein. More importantly, investigations on the synthetic system and formation mechanism of porous MMOs will be highlighted. Some future trends for the innovative design of new electrode materials are also discussed in this review. The challenges and prospects will draw many researchers' attention.

  15. Porous anodic alumina on galvanically grown PtSi layer for application in template-assisted Si nanowire growth

    NASA Astrophysics Data System (ADS)

    Michelakaki, Irini; Nassiopoulou, Androula G.; Stavrinidou, Eleni; Breza, Katerina; Frangis, Nikos

    2011-06-01

    We report on the fabrication and morphology/structural characterization of a porous anodic alumina (PAA)/PtSi nano-template for use as matrix in template-assisted Si nanowire growth on a Si substrate. The PtSi layer was formed by electroless deposition from an aqueous solution containing the metal salt and HF, while the PAA membrane by anodizing an Al film deposited on the PtSi layer. The morphology and structure of the PtSi layer and of the alumina membrane on top were studied by Scanning and High Resolution Transmission Electron Microscopies (SEM, HRTEM). Cross sectional HRTEM images combined with electron diffraction (ED) were used to characterize the different interfaces between Si, PtSi and porous anodic alumina.

  16. Application of 8YSZ Nanopowder Synthesized by the Modified Solvothermal Process for Anode Supported Solid Oxide Fuel Cells.

    PubMed

    Meepho, Malinee; Wattanasiriwech, Suthee; Angkavatana, Pavadee; Wattanasiriwech, Darunee

    2015-03-01

    Thin electrolyte yttria-stabilized zirconia (8YSZ) films were coated on the porous solid oxide fuel cell (SOFC) anode substrates for the use at an intermediate temperature range. Nano-8YSZ powder with a particle size of about 5 nm was synthesized using the modified solvothermal process. The electrolyte suspension was prepared by dispersion the synthesized 8YSZ nanopowder in ethanol, with PVB and 1,3-propanediol as a binder and a charging agent respectively. The 8YSZ suspension was subsequently deposited on the pre-sintered NiO-YSZ porous substrates by the electrophoretic deposition (EPD) technique. In order to obtain high quality electrolyte films, preparation process was optimized through two strategic approaches; (i) adjustment of suspension's rheological property and (ii) compatibility of anode-electrolyte sintering shrinkage. Rheological property of the suspension was improved with an addition of 1,3-propanediol. The zeta potential of this suspension was increased and reached the value of +24 mV so the well-dispersed slurry was finally obtained. The second approach was achieved by using a proper composite anode powders. Dense and uniform 8YSZ electrolyte films with a thickness of about 1 thickness successfully be formed on the NiO-YSZ porous substrates after co-sintering at 1400 °C for 2 h. PMID:26413707

  17. Properties and composition of anodic oxide layers of indium antimonide

    SciTech Connect

    Sorokin, I.N.; Gat'ko, L.E.; Nikitina, N.G.

    1985-09-01

    In recent years a number of optoelectronic devices based on narrowgap semiconductors of the AIIIBV type have been developed. One of the factors preventing widespread production of such devices is the inadequate study of the effect of the technology on the properties of insulator-semiconductor systems, of which anodic oxide films (AOF)--indium antimonide--are most promising. In this work the authors studied the dielectric properties and chemical composition of indium antimonide AOF as a function of their thicknesses and conditions of formation. It is determined that anodic indium antimonide oxide layers 90-110nm thick have high dielectric properties. It is also determined that an increase of the film thickness above 80100nm is accompanied by a decrease in the relative antimony content. The ratio of indium and antimony in oxide layers depends on the electrical conditions of oxidation of the semiconductor: the relative antimony content increases as a result of a decrease in the field intensity under conditions of constant voltage.

  18. Terbium luminescence in alumina xerogel fabricated in porous anodic alumina matrix under various excitation conditions

    SciTech Connect

    Gaponenko, N. V.; Kortov, V. S.; Orekhovskaya, T. I.; Nikolaenko, I. A.; Pustovarov, V. A.; Zvonarev, S. V.; Slesarev, A. I.; Prislopski, S. Ya.

    2011-07-15

    Terbium-doped alumina xerogel layers are synthesized by the sol-gel method in pores of a porous anodic alumina film 1 {mu}m thick with a pore diameter of 150-180 nm; the film is grown on a silicon substrate. The fabricated structures exhibit terbium photoluminescence with bands typical of trivalent terbium terms. Terbium X-ray luminescence with the most intense band at 542 nm is observed for the first time for such a structure. Morphological analysis of the structure by scanning electron microscopy shows the presence of xerogel clusters in pore channels, while the main pore volume remains unfilled and pore mouths remain open. The data obtained confirm the promising applications of fabricated structures for developing matrix converters of X-rays and other ionizing radiations into visible light. The possibilities of increasing luminescence intensity in the matrix converter are discussed.

  19. Structural and wetting properties of porous anodic alumina templates prepared by different electrolytes

    NASA Astrophysics Data System (ADS)

    Suchitra S., M.; Reddy, P. Ramana; Udayashankar, N. K.

    2016-05-01

    Porous anodic alumina (PAA) has been extensively studied in recent years due to their unique properties and applications for manufacturing nanostructured materials. In this article, we report our studies on structural and wetting properties of PAA membranes prepared using different electrolytes such as sulphuric, oxalic and phosphoric acids. The morphological parameters such as pore diameter and porosity were measured using SEM and analysed using image-J software. The structural investigation of PAA membranes was carried out through X-ray diffraction analysis and it was confirmed that PAA membranes were amorphous in nature. The wetting behaviour of PAA membranes were measured using contact angle measurement technique. The results show that PAA membranes were hydrophilic in nature with contact angles 26.03°, 35.21° and 42.0° for sulphuric, oxalic and phosphoric acids respectively.

  20. Electrochemical fabrication of 2D and 3D nickel nanowires using porous anodic alumina templates

    NASA Astrophysics Data System (ADS)

    Mebed, A. M.; Abd-Elnaiem, Alaa M.; Al-Hosiny, Najm M.

    2016-06-01

    Mechanically stable nickel (Ni) nanowires array and nanowires network were synthesized by pulse electrochemical deposition using 2D and 3D porous anodic alumina (PAA) templates. The structures and morphologies of as-prepared films were characterized by X-ray diffraction and scanning electron microscopy, respectively. The grown Ni nanowire using 3D PAA revealed more strength and larger surface area than has grown Ni use 2D PAA template. The prepared nanowires have a face-centered cubic crystal structure with average grain size 15 nm, and the preferred orientation of the nucleation of the nanowires is (111). The diameter of the nanowires is about 50-70 nm with length 3 µm. The resulting 3D Ni nanowire lattice, which provides enhanced mechanical stability and an increased surface area, benefits energy storage and many other applications which utilize the large surface area.

  1. Fabrication and optical property of metal nanowire arrays embedded in anodic porous alumina membrane

    NASA Astrophysics Data System (ADS)

    Takase, Kouichi; Shimizu, Tomohiro; Sugawa, Kosuke; Aono, Takashige; Shirai, Yuma; Nishida, Tomohiko; Shingubara, Shoso

    2016-06-01

    Nanowires embedded in nanopores are potentially tough against surface scraping and agglomeration. In this study, we have fabricated Au and Ni nanowires embedded into anodic porous alumina (APA) and investigated their reflectance to study the effects of surface plasmon absorption properties and conversion from solar energy to thermal energy. Au nanowires embedded into APA show typical gold surface plasmon absorption at approximately 530 nm. On the other hand, Ni nanowires show quite a low reflectance under 600 nm. In the temperature elevation test, both Au and Ni nanowire samples present the same capability to warm up water. It means that Ni nanowires embedded into APA have almost the same photothermal activity as Au nanowires.

  2. Formation and disruption of current paths of anodic porous alumina films by conducting atomic force microscopy

    NASA Astrophysics Data System (ADS)

    Oyoshi, K.; Nigo, S.; Inoue, J.; Sakai, O.; Kitazawa, H.; Kido, G.

    2010-11-01

    Anodic porous alumina (APA) films have a honeycomb cell structure of pores and a voltage-induced bi-stable switching effect. We have applied conducting atomic force microscopy (CAFM) as a method to form and to disrupt current paths in the APA films. A bi-polar switching operation was confirmed. We have firstly observed terminals of current paths as spots or areas typically on the center of the triangle formed by three pores. In addition, though a part of the current path showed repetitive switching, most of them were not observed again at the same position after one cycle of switching operations in the present experiments. This suggests that a part of alumina structure and/or composition along the current paths is modified during the switching operations.

  3. Electrolytic LiCl precipitation from LiCl-KCl melt in porous Li-Al anodes

    NASA Astrophysics Data System (ADS)

    Vallet, C. E.; Heatherly, D. E.; Heatherly, L., Jr.; Braunstein, J.

    1983-12-01

    Composition gradients such as those predicted to occur during discharge of porous Li-Al negative electrodes of Li/S batteries with LiCl-KCl eutectic electrolyte were generated and measured in the LiCl-KCl anolyte of an electrolysis cell with Li-Al electrodes. Precipitation of lithium chloride during electrolysis was observed by two-dimensional scanning of electrolyte composition in the front part of quenched porous Li-Al anode sections using SEM/EDX. The distribution of sites of increased or decreased LiCl concentration, LiCl saturation and precipitation was mapped. Cathodic regions were observed near the cell walls. Preliminary results of analysis by Auger spectroscopy confirm LiCl precipitation in the porous anode.

  4. Porous cubes constructed by cobalt oxide nanocrystals with graphene sheet coatings for enhanced lithium storage properties.

    PubMed

    Geng, Hongbo; Guo, Yuanyuan; Ding, Xianguang; Wang, Huangwen; Zhang, Yufei; Wu, Xinglong; Jiang, Jiang; Zheng, Junwei; Yang, Yonggang; Gu, Hongwei

    2016-04-14

    In this manuscript, graphene-encapsulated porous cobalt oxide cubes (Co3O4@G) are fabricated through a facile precipitation reaction with subsequent calcination and a self-assembly process. The synthesized porous Co3O4 cubes anchored in the conductive graphene network can realize superior electrical conductivity, withstand volume variation upon prolonged cycling and shorten the diffusion path of lithium ions. When evaluated as anode materials, the Co3O4@G electrode shows excellent electrochemical properties in terms of both stable cycling performance and good rate capabilities. For example, a reversible discharge capacity of 980 mA h g(-1) is delivered after 80 cycles at a current density of 200 mA g(-1). Introducing a conductive graphene network to modify other metal oxides with poor electric conductivity and large volume excursions is of great interest in the development of lithium ion battery technologies. PMID:26997536

  5. Image measurements of unsteady pressure fluctuation by a pressure-sensitive coating on porous anodized aluminium

    NASA Astrophysics Data System (ADS)

    Kameda, M.; Tabei, T.; Nakakita, K.; Sakaue, H.; Asai, K.

    2005-12-01

    Pressure-sensitive luminescent coating on porous anodized aluminium (AA-PSP) was applied to measure non-periodic unsteady pressure distribution on a wind-tunnel model. A high-speed digital video camera was used to capture the PSP signal. The pressure-sensitive dye was tris(4,7-diphenylphenanthroline) ruthenium(II) ([Ru(dpp)3]2+). The coating has a short response time of O(10 µs), although it exhibits temperature and humidity sensitivities. A hydrophobic coating was applied on the anodized aluminium surface to suppress the humidity sensitivity. A temperature sensitive paint was used to obtain the temperature distribution instantaneously with the pressure. The temperature data were used to correct the PSP response. An appropriate data acquisition procedure as well as digital image processing algorithm was established to compensate for the error from the temperature and humidity sensitivities. The present system was applied to measure the pressure distribution on a delta wing at a high angle of attack in transonic flow, whose flow is unsteady due to the interaction between shock waves and leading edge vortices. The non-periodic unsteady pressure distribution on the delta wing was successfully measured with the sampling rate of 1 kHz and within a few per cent error in absolute pressure level.

  6. In vitro apatite formation on porous anodic alumina induced by a phosphorylation treatment.

    PubMed

    Li, Xiaohong; Ni, Siyu; Webster, Thomas J

    2014-09-01

    In this study, a phosphorylation treatment of porous anodic alumina (PAA) was performed by wet impregnation in phosphoric acid and a subsequent heat treatment. The PAA and phosphorylated PAA specimens were analyzed using a field emission scanning electron microscope, an energy-dispersive X-ray spectrometer, and Fourier transform infrared spectroscopy. The apatite-forming ability of the phosphorylated PAA was evaluated by soaking the specimens in simulated body fluid for 1, 3, and 7 days. The surface microstructures and chemical property changes after soaking in simulated body fluid were again characterized by field emission scanning electron microscope, energy-dispersive X-ray spectrometer, and Fourier transform infrared spectroscopy. Results of this study demonstrated that the functional -PO4 groups introduced onto the PAA surface dramatically promoted the deposition of bone-like apatite on PAA. The results from this study indicated that the phosphorylation treatment of anodic alumina is an effective method for inducing bone-like apatite formation, and this phosphorylated PAA can be a promising candidate to be used as bioactive surface coatings on implant metals and alloys for orthopedic and dental applications. PMID:24598060

  7. Solid oxide fuel cell bi-layer anode with gadolinia-doped ceria for utilization of solid carbon fuel

    NASA Astrophysics Data System (ADS)

    Kellogg, Isaiah D.; Koylu, Umit O.; Dogan, Fatih

    Pyrolytic carbon was used as fuel in a solid oxide fuel cell (SOFC) with a yttria-stabilized zirconia (YSZ) electrolyte and a bi-layer anode composed of nickel oxide gadolinia-doped ceria (NiO-GDC) and NiO-YSZ. The common problems of bulk shrinkage and emergent porosity in the YSZ layer adjacent to the GDC/YSZ interface were avoided by using an interlayer of porous NiO-YSZ as a buffer anode layer between the electrolyte and the NiO-GDC primary anode. Cells were fabricated from commercially available component powders so that unconventional production methods suggested in the literature were avoided, that is, the necessity of glycine-nitrate combustion synthesis, specialty multicomponent oxide powders, sputtering, or chemical vapor deposition. The easily-fabricated cell was successfully utilized with hydrogen and propane fuels as well as carbon deposited on the anode during the cyclic operation with the propane. A cell of similar construction could be used in the exhaust stream of a diesel engine to capture and utilize soot for secondary power generation and decreased particulate pollution without the need for filter regeneration.

  8. Infiltrated lanthanum strontium chromite anodes for solid oxide fuel cells: Structural and catalytic aspects

    NASA Astrophysics Data System (ADS)

    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.

  9. Steam reforming of methanol over copper loaded anodized aluminum oxide (AAO) prepared through electrodeposition

    NASA Astrophysics Data System (ADS)

    Linga Reddy, E.; Karuppiah, J.; Lee, Hyun Chan; Kim, Dong Hyun

    2014-12-01

    In order to study the steam reforming of methanol (SRM) to produce hydrogen for fuel cells, porous γ-alumina support is developed on Al substrate using anodic oxidation process and copper catalyst particles are deposited homogeneously over anodic aluminum oxide (AAO) surface by electrodeposition method. We investigated the effect of electrodeposition time and hot water treatment (HWT) on the activity of catalysts for SRM reaction in the temperature range between 160 and 360 °C. The experimental results indicate that the SRM activity, CO2 and dimethyl ether (DME) selectivity's over Cu catalysts increased as the electrodeposition time increased from 30 to 120 s, further increment in deposition time of Cu have no significant effect on it. The rates of SRM conversion are found to be higher for the catalysts made from the supports obtained after HWT, which may be due to the enhancement in the surface area of AAO support. It is found that the SRM activity and CO2 selectivity strongly depended upon the free exposed copper sites available for methanol adsorption and reaction, and DME in products is mainly observed in the reaction temperature range between 300 and 350 °C and it is higher for the catalysts with low Cu content.

  10. Anodic aluminum oxide with fine pore size control for selective and effective particulate matter filtering

    NASA Astrophysics Data System (ADS)

    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. Analysis of nanopore arrangement of porous alumina layers formed by anodizing in oxalic acid at relatively high temperatures

    NASA Astrophysics Data System (ADS)

    Zaraska, Leszek; Stępniowski, Wojciech J.; Jaskuła, Marian; Sulka, Grzegorz D.

    2014-06-01

    Anodic aluminum oxide (AAO) layers were formed by a simple two-step anodization in 0.3 M oxalic acid at relatively high temperatures (20-30 °C) and various anodizing potentials (30-65 V). The effect of anodizing conditions on structural features of as-obtained oxides was carefully investigated. A linear and exponential relationships between cell diameter, pore density and anodizing potential were confirmed, respectively. On the other hand, no effect of temperature and duration of anodization on pore spacing and pore density was found. Detailed quantitative and qualitative analyses of hexagonal arrangement of nanopore arrays were performed for all studied samples. The nanopore arrangement was evaluated using various methods based on the fast Fourier transform (FFT) images, Delaunay triangulations (defect maps), pair distribution functions (PDF), and angular distribution functions (ADF). It was found that for short anodizations performed at relatively high temperatures, the optimal anodizing potential that results in formation of nanostructures with the highest degree of pore order is 45 V. No direct effect of temperature and time of anodization on the nanopore arrangement was observed.

  12. Porous cubes constructed by cobalt oxide nanocrystals with graphene sheet coatings for enhanced lithium storage properties

    NASA Astrophysics Data System (ADS)

    Geng, Hongbo; Guo, Yuanyuan; Ding, Xianguang; Wang, Huangwen; Zhang, Yufei; Wu, Xinglong; Jiang, Jiang; Zheng, Junwei; Yang, Yonggang; Gu, Hongwei

    2016-03-01

    In this manuscript, graphene-encapsulated porous cobalt oxide cubes (Co3O4@G) are fabricated through a facile precipitation reaction with subsequent calcination and a self-assembly process. The synthesized porous Co3O4 cubes anchored in the conductive graphene network can realize superior electrical conductivity, withstand volume variation upon prolonged cycling and shorten the diffusion path of lithium ions. When evaluated as anode materials, the Co3O4@G electrode shows excellent electrochemical properties in terms of both stable cycling performance and good rate capabilities. For example, a reversible discharge capacity of 980 mA h g-1 is delivered after 80 cycles at a current density of 200 mA g-1. Introducing a conductive graphene network to modify other metal oxides with poor electric conductivity and large volume excursions is of great interest in the development of lithium ion battery technologies.In this manuscript, graphene-encapsulated porous cobalt oxide cubes (Co3O4@G) are fabricated through a facile precipitation reaction with subsequent calcination and a self-assembly process. The synthesized porous Co3O4 cubes anchored in the conductive graphene network can realize superior electrical conductivity, withstand volume variation upon prolonged cycling and shorten the diffusion path of lithium ions. When evaluated as anode materials, the Co3O4@G electrode shows excellent electrochemical properties in terms of both stable cycling performance and good rate capabilities. For example, a reversible discharge capacity of 980 mA h g-1 is delivered after 80 cycles at a current density of 200 mA g-1. Introducing a conductive graphene network to modify other metal oxides with poor electric conductivity and large volume excursions is of great interest in the development of lithium ion battery technologies. Electronic supplementary information (ESI) available. See DOI: 10.1039/c6nr01024e

  13. Graphene-Assisted Chemical Etching of Silicon Using Anodic Aluminum Oxides as Patterning Templates.

    PubMed

    Kim, Jungkil; Lee, Dae Hun; Kim, Ju Hwan; Choi, Suk-Ho

    2015-11-01

    We first report graphene-assisted chemical etching (GaCE) of silicon by using patterned graphene as an etching catalyst. Chemical-vapor-deposition-grown graphene transferred on a silicon substrate is patterned to a mesh with nanohole arrays by oxygen plasma etching using an anodic- aluminum-oxide etching mask. The prepared graphene mesh/silicon is immersed in a mixture solution of hydrofluoric acid and hydro peroxide with various molecular fractions at optimized temperatures. The silicon underneath graphene mesh is then selectively etched to form aligned nanopillar arrays. The morphology of the nanostructured silicon can be controlled to be smooth or porous depending on the etching conditions. The experimental results are systematically discussed based on possible mechanisms for GaCE of Si. PMID:26473800

  14. Hierarchical Sandwich-Like Structure of Ultrafine N-Rich Porous Carbon Nanospheres Grown on Graphene Sheets as Superior Lithium-Ion Battery Anodes.

    PubMed

    Xie, Zhiqiang; He, Ziyang; Feng, Xuhui; Xu, Wangwang; Cui, Xiaodan; Zhang, Jiuhong; Yan, Cheng; Carreon, Moises A; Liu, Zheng; Wang, Ying

    2016-04-27

    A sandwich-like, graphene-based porous nitrogen-doped carbon (PNCs@Gr) has been prepared through facile pyrolysis of zeolitic imidazolate framework nanoparticles in situ grown on graphene oxide (GO) (ZIF-8@GO). Such sandwich-like nanostructure can be used as anode material in lithium ion batteries, exhibiting remarkable capacities, outstanding rate capability, and cycling performances that are some of the best results among carbonaceous electrode materials and exceed most metal oxide-based anode materials derived from metal orgainc frameworks (MOFs). Apart from a high initial capacity of 1378 mAh g(-1) at 100 mA g(-1), this PNCs@Gr electrode can be cycled at high specific currents of 500 and 1000 mA g(-1) with very stable reversible capacities of 1070 and 948 mAh g(-1) to 100 and 200 cycles, respectively. At a higher specific current of 5000 mA g(-1), the electrode still delivers a reversible capacity of over 530 mAh g(-1) after 400 cycles, showing a capacity retention of as high as 84.4%. Such an impressive electrochemical performance is ascribed to the ideal combination of hierarchically porous structure, a highly conductive graphene platform, and high-level nitrogen doping in the sandwich-like PNCs@Gr electrode obtained via in situ synthesis. PMID:27071473

  15. Kinetic features of the oxide formation on {111} polar planes upon anode treatment of n-GaAs

    NASA Astrophysics Data System (ADS)

    Orlov, A. M.; Yavtushenko, I. O.; Makhmud-Akhunov, M. Yu.

    2016-04-01

    The mechanism and kinetics of anode destruction of {111} polar planes of n-GaAs and morphological features of forming oxide films in the potentiostatic mode of polarization in weakly acid solutions of electrolytes have been studied. It has been found that anode polarization of the gallium plane (111) Ga provides the formation of a porous structure of both the single-crystal matrix and oxide film, which has a planar topology. In this case, the pore density is always commensurable with the surface dope concentration. In contrast to the gallium plane, the anode polarization of the arsenic plane overline {( {111} )} As provides the tangential mechanism of destruction of the semiconductor matrix and the island-type morphology of the oxide. Equal crystallographic orientation of islands is determined by the directive action of the family of oxidized planes { {1overline {11} } } GaAs. However, regardless of the crystallographic orientation of the polar plane, the forming oxide is represented by polycrystalline As2O3 and amorphous Ga2O3.

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

    NASA Astrophysics Data System (ADS)

    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.

  17. Hierarchical porous nickel oxide-carbon nanotubes as advanced pseudocapacitor materials for supercapacitors

    NASA Astrophysics Data System (ADS)

    Su, Aldwin D.; Zhang, Xiang; Rinaldi, Ali; Nguyen, Son T.; Liu, Huihui; Lei, Zhibin; Lu, Li; Duong, Hai M.

    2013-03-01

    Hierarchical porous carbon anode and metal oxide cathode are promising for supercapacitor with both high energy density and high power density. This Letter uses NiO and commercial carbon nanotubes (CNTs) as electrode materials for electrochemical capacitors with high energy storage capacities. Experimental results show that the specific capacitance of the electrode materials for 10%, 30% and 50% CNTs are 279, 242 and 112 F/g, respectively in an aqueous 1 M KOH electrolyte at a charge rate of 0.56 A/g. The maximum specific capacitance is 328 F/g at a charge rate of 0.33 A/g.

  18. Oxidation behaviors of porous Haynes 214 alloy at high temperatures

    SciTech Connect

    Wang, Yan; Liu, Yong; Tang, Huiping; Li, Weijie

    2015-09-15

    The oxidation behaviors of porous Haynes 214 alloy at temperatures from 850 to 1000 °C were investigated. The porous alloys before and after the oxidation were examined by optical microscopy, scanning electron microscopy (SEM) and energy dispersive spectroscopy (EDS), X-ray diffraction (XRD) analyses, and X-ray photoelectron spectroscopy (XPS). The oxidation kinetics of the porous alloy approximately follows a parabolic rate law and exhibits two stages controlled by different oxidation courses. Complex oxide scales composed of Cr{sub 2}O{sub 3}, NiCr{sub 2}O{sub 4} and Al{sub 2}O{sub 3} are formed on the oxidized porous alloys, and the formation of Cr{sub 2}O{sub 3} on its outer layer is promoted with the oxidation proceeding. The rough surface as well as the micropores in the microstructures of the porous alloy caused by the manufacturing process provides fast diffusion paths for oxygen so as to affect the formation of the oxide layers. Both the maximum pore size and the permeability of the porous alloys decrease with the increase of oxidation temperature and exposure time, which may limit its applications. - Highlights: • Two-stage oxidation kinetics controlled by different oxidation courses is showed. • Oxide scale mainly consists of Cr{sub 2}O{sub 3}, NiCr{sub 2}O{sub 4} and Al{sub 2}O{sub 3}. • Rough surface and micropores lead to the formation of uneven oxide structure. • Content of Cr{sub 2}O{sub 3} in the outer layer of the scale increases with time at 1000 °C. • Maximum pore size and permeability decrease with increasing temperature and time.

  19. Comparative study on ammonia oxidation over Ni-based cermet anodes for solid oxide fuel cells

    NASA Astrophysics Data System (ADS)

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

    2016-02-01

    In the current work, we investigate the performance of solid oxide fuel cells (SOFCs) with Ni‒yttria-stabilized zirconia (Ni-YSZ) and Ni‒gadolinia-dope ceria (Ni-GDC) cermet anodes fueled with H2 or NH3 in terms of the catalytic activity of ammonia decomposition. The cermet of Ni-GDC shows higher catalytic activity for ammonia decomposition than Ni-YSZ. In response to this, the performance of direct NH3-fueled SOFC improved by using Ni-GDC anode. Moreover, we observe further enhancement in the cell performance and the catalytic activity for ammonia decomposition with applying Ni-GDC anode synthesised by the glycine-nitrate combustion process. These results reveal that the high performance of Ni-GDC anode for the direct NH3-fueled SOFC results from its mixed ionic-electronic conductivity as well as high catalytic activity for ammonia decomposition.

  20. Anodic deposition of hydrous ruthenium oxide for supercapacitors

    NASA Astrophysics Data System (ADS)

    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.

  1. Ultra-high density single nanometer-scale anodic alumina nanofibers fabricated by pyrophosphoric acid anodizing.

    PubMed

    Kikuchi, Tatsuya; Nishinaga, Osamu; Nakajima, Daiki; Kawashima, Jun; Natsui, Shungo; Sakaguchi, Norihito; Suzuki, Ryosuke O

    2014-01-01

    Anodic oxide fabricated by anodizing has been widely used for nanostructural engineering, but the nanomorphology is limited to only two oxides: anodic barrier and porous oxides. Therefore, the discovery of an additional anodic oxide with a unique nanofeature would expand the applicability of anodizing. Here we demonstrate the fabrication of a third-generation anodic oxide, specifically, anodic alumina nanofibers, by anodizing in a new electrolyte, pyrophosphoric acid. Ultra-high density single nanometer-scale anodic alumina nanofibers (10(10) nanofibers/cm(2)) consisting of an amorphous, pure aluminum oxide were successfully fabricated via pyrophosphoric acid anodizing. The nanomorphologies of the anodic nanofibers can be controlled by the electrochemical conditions. Anodic tungsten oxide nanofibers can also be fabricated by pyrophosphoric acid anodizing. The aluminum surface covered by the anodic alumina nanofibers exhibited ultra-fast superhydrophilic behavior, with a contact angle of less than 1°, within 1 second. Such ultra-narrow nanofibers can be used for various nanoapplications including catalysts, wettability control, and electronic devices. PMID:25491282

  2. Ultra-High Density Single Nanometer-Scale Anodic Alumina Nanofibers Fabricated by Pyrophosphoric Acid Anodizing

    NASA Astrophysics Data System (ADS)

    Kikuchi, Tatsuya; Nishinaga, Osamu; Nakajima, Daiki; Kawashima, Jun; Natsui, Shungo; Sakaguchi, Norihito; Suzuki, Ryosuke O.

    2014-12-01

    Anodic oxide fabricated by anodizing has been widely used for nanostructural engineering, but the nanomorphology is limited to only two oxides: anodic barrier and porous oxides. Therefore, the discovery of an additional anodic oxide with a unique nanofeature would expand the applicability of anodizing. Here we demonstrate the fabrication of a third-generation anodic oxide, specifically, anodic alumina nanofibers, by anodizing in a new electrolyte, pyrophosphoric acid. Ultra-high density single nanometer-scale anodic alumina nanofibers (1010 nanofibers/cm2) consisting of an amorphous, pure aluminum oxide were successfully fabricated via pyrophosphoric acid anodizing. The nanomorphologies of the anodic nanofibers can be controlled by the electrochemical conditions. Anodic tungsten oxide nanofibers can also be fabricated by pyrophosphoric acid anodizing. The aluminum surface covered by the anodic alumina nanofibers exhibited ultra-fast superhydrophilic behavior, with a contact angle of less than 1°, within 1 second. Such ultra-narrow nanofibers can be used for various nanoapplications including catalysts, wettability control, and electronic devices.

  3. Ultra-High Density Single Nanometer-Scale Anodic Alumina Nanofibers Fabricated by Pyrophosphoric Acid Anodizing

    PubMed Central

    Kikuchi, Tatsuya; Nishinaga, Osamu; Nakajima, Daiki; Kawashima, Jun; Natsui, Shungo; Sakaguchi, Norihito; Suzuki, Ryosuke O.

    2014-01-01

    Anodic oxide fabricated by anodizing has been widely used for nanostructural engineering, but the nanomorphology is limited to only two oxides: anodic barrier and porous oxides. Therefore, the discovery of an additional anodic oxide with a unique nanofeature would expand the applicability of anodizing. Here we demonstrate the fabrication of a third-generation anodic oxide, specifically, anodic alumina nanofibers, by anodizing in a new electrolyte, pyrophosphoric acid. Ultra-high density single nanometer-scale anodic alumina nanofibers (1010 nanofibers/cm2) consisting of an amorphous, pure aluminum oxide were successfully fabricated via pyrophosphoric acid anodizing. The nanomorphologies of the anodic nanofibers can be controlled by the electrochemical conditions. Anodic tungsten oxide nanofibers can also be fabricated by pyrophosphoric acid anodizing. The aluminum surface covered by the anodic alumina nanofibers exhibited ultra-fast superhydrophilic behavior, with a contact angle of less than 1°, within 1 second. Such ultra-narrow nanofibers can be used for various nanoapplications including catalysts, wettability control, and electronic devices. PMID:25491282

  4. Performance studies of copper-iron/ceria-yttria stabilized zirconia anode for electro-oxidation of butane in solid oxide fuel cells

    NASA Astrophysics Data System (ADS)

    Kaur, Gurpreet; Basu, Suddhasatwa

    2013-11-01

    Addition of second metal to Cu is useful for electro-oxidation of hydrocarbons in solid oxide fuel cells (SOFC). In this work, electro-catalysts based on Cu-Fe bimetallic anode for use of both H2 and n-C4H10 in SOFC is prepared by wet impregnation method into a porous CeO2-YSZ matrix. The prepared Cu-Fe/CeO2-YSZ anodes are then characterized by thermo-gravimetric analysis (TGA), X-ray diffraction (XRD), elemental dispersive X-ray (EDX) and scanning electron microscopy (SEM). Carbonaceous deposits formed on Cu-Fe/CeO2-YSZ anodes after exposure to n-C4H10 are studied using a combination of i-V characteristics and TGA measurements. It is observed that the addition of Fe to Cu in CeO2-YSZ cermet anode enhance the performance in H2 and n-C4H10 fuels. The performance of cell having molar ratio of Cu-Fe of 1:1 in Cu-Fe/CeO2-YSZ anode shows power density of 240 mW cm-2 and 260 mW cm-2 in n-C4H10 and in H2 after n-C4H10 flow at 800 °C. The i-V curve shows that the conductivity of the anode improves after exposure to n-C4H10. No apparent degradation in performance is observed after n-C4H10 flow except for carbon fibre formation indicating Cu-Fe bimetallic is worth considering as an anode for direct butane SOFC.

  5. Preparation of Aluminum Nanomesh Thin Films from an Anodic Aluminum Oxide Template as Transparent Conductive Electrodes

    NASA Astrophysics Data System (ADS)

    Li, Yiwen; Chen, Yulong; Qiu, Mingxia; Yu, Hongyu; Zhang, Xinhai; Sun, Xiao Wei; Chen, Rui

    2016-02-01

    We have employed anodic aluminum oxide as a template to prepare ultrathin, transparent, and conducting Al films with a unique nanomesh structure for transparent conductive electrodes. The anodic aluminum oxide template is obtained through direct anodization of a sputtered Al layer on a glass substrate, and subsequent wet etching creates the nanomesh metallic film. The optical and conductive properties are greatly influenced by experimental conditions. By tuning the anodizing time, transparent electrodes with appropriate optical transmittance and sheet resistance have been obtained. The results demonstrate that our proposed strategy can serve as a potential method to fabricate low-cost TCEs to replace conventional indium tin oxide materials.

  6. Preparation of Aluminum Nanomesh Thin Films from an Anodic Aluminum Oxide Template as Transparent Conductive Electrodes.

    PubMed

    Li, Yiwen; Chen, Yulong; Qiu, Mingxia; Yu, Hongyu; Zhang, Xinhai; Sun, Xiao Wei; Chen, Rui

    2016-01-01

    We have employed anodic aluminum oxide as a template to prepare ultrathin, transparent, and conducting Al films with a unique nanomesh structure for transparent conductive electrodes. The anodic aluminum oxide template is obtained through direct anodization of a sputtered Al layer on a glass substrate, and subsequent wet etching creates the nanomesh metallic film. The optical and conductive properties are greatly influenced by experimental conditions. By tuning the anodizing time, transparent electrodes with appropriate optical transmittance and sheet resistance have been obtained. The results demonstrate that our proposed strategy can serve as a potential method to fabricate low-cost TCEs to replace conventional indium tin oxide materials. PMID:26831759

  7. Preparation of Aluminum Nanomesh Thin Films from an Anodic Aluminum Oxide Template as Transparent Conductive Electrodes

    PubMed Central

    Li, Yiwen; Chen, Yulong; Qiu, Mingxia; Yu, Hongyu; Zhang, Xinhai; Sun, Xiao Wei; Chen, Rui

    2016-01-01

    We have employed anodic aluminum oxide as a template to prepare ultrathin, transparent, and conducting Al films with a unique nanomesh structure for transparent conductive electrodes. The anodic aluminum oxide template is obtained through direct anodization of a sputtered Al layer on a glass substrate, and subsequent wet etching creates the nanomesh metallic film. The optical and conductive properties are greatly influenced by experimental conditions. By tuning the anodizing time, transparent electrodes with appropriate optical transmittance and sheet resistance have been obtained. The results demonstrate that our proposed strategy can serve as a potential method to fabricate low-cost TCEs to replace conventional indium tin oxide materials. PMID:26831759

  8. Crystal structure and nanotopographical features on the surface of heat-treated and anodized porous titanium biomaterials produced using selective laser melting

    NASA Astrophysics Data System (ADS)

    Amin Yavari, S.; Wauthle, R.; Böttger, A. J.; Schrooten, J.; Weinans, H.; Zadpoor, A. A.

    2014-01-01

    Porous titanium biomaterials manufactured using additive manufacturing techniques such as selective laser melting are considered promising materials for orthopedic applications where the biomaterial needs to mimic the properties of bone. Despite their appropriate mechanical properties and the ample pore space they provide for bone ingrowth and osseointegration, porous titanium structures have an intrinsically bioinert surface and need to be subjected to surface bio-functionalizing procedures to enhance their in vivo performance. In this study, we used a specific anodizing process to build a hierarchical oxide layer on the surface of porous titanium structures made by selective laser melting of Ti6Al4V ELI powder. The hierarchical structure included both nanotopographical features (nanotubes) and micro-features (micropits). After anodizing, the biomaterial was heat treated in Argon at different temperatures ranging between 400 and 600 °C for either 1 or 2 h to improve its bioactivity. The effects of applied heat treatment on the crystal structure of TiO2 nanotubes and the nanotopographical features of the surface were studied using scanning electron microscopy and X-ray diffraction. It was shown that the transition from the initial crystal structure, i.e. anatase, to rutile occurs between 500 and 600 °C and that after 2 h of heat treatment at 600 °C the crystal structure is predominantly rutile. The nanotopographical features of the surface were found to be largely unchanged for heat treatments carried out at 500 °C or below, whereas they were partially or largely disrupted after heat treatment at 600 °C. The possible implications of these findings for the bioactivity of porous titanium structures are discussed.

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

    DOEpatents

    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).

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

    SciTech Connect

    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

  11. Effect of annealing on photoluminescence and optical properties of porous anodic alumina films formed in sulfuric acid for solar energy applications

    NASA Astrophysics Data System (ADS)

    Ghrib, Mondher; Ouertani, Rachid; Gaidi, Monir; Khedher, Najoua; Salem, Mohamed Ben; Ezzaouia, Hatem

    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 °C. Photoluminescence (PL) measurements show two PL peaks in the emission and excitation spectra. The first emission peak is centered at 460 nm (α-band) and the second (β-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.

  12. An unexpected large capacity of ultrafine manganese oxide as a sodium-ion battery anode.

    PubMed

    Weng, Yu-Ting; Huang, Tzu-Yang; Lim, Chek-Hai; Shao, Pei-Sian; Hy, Sunny; Kuo, Chao-Yen; Cheng, Ju-Hsiang; Hwang, Bing-Joe; Lee, Jyh-Fu; Wu, Nae-Lih

    2015-12-21

    MnO2 is shown for the first time to be electrochemically active as a conversion anode for Na-ion batteries (NIBs). Space-confined ultrafine (UF)-MnO2, with an average crystal size of 4 nm, synthesized using a porous silicon dioxide templated hydrothermal process exhibits a high reversible sodiation capacity of 567 mA h g(-1), in contrast to the negligible activity shown by the aggregates of larger (14 nm) MnO2 nanocrystallites. The remarkably enhanced sodiation activity of the UF-MnO2 is attributable to its greatly reduced crystal size, which facilitates diffusion of Na ions, along with high surface energy arising from extensive heterogeneous interfacial bonding with the SiO2 surrounding. The UF-MnO2 anode exhibits an exceptional rate and cycle performance, exhibiting >70% capacity retention after 500 cycles. In operando synchrotron X-ray absorption near-edge structural analysis reveals combined charge-storage mechanisms involving conversion reaction between Mn(III) and Mn(II) oxides, Mn(III)-O1.5 + Na(+) + e(-)- ↔ 1/2Na2O + Mn(II)-O, and non-Mn-centered redox reactions. The finding suggests a new strategy for "activating" the potential electrochemical electrode materials that appear inactive in the bulk form. PMID:26567463

  13. Porous Ni0.14Mn0.86O1.43 hollow microspheres as high-performing anodes for lithium-ion batteries

    NASA Astrophysics Data System (ADS)

    Ma, Zhong; Yuan, Xianxia; Li, Lin; Ma, Zi-Feng; Zhang, Lei; Mai, Liqiang; Zhang, Jiujun

    2015-09-01

    A uniformly dispersed bi-component nanocompotise of transition metal oxide (Mn2O3)/mixed transition metal oxide (NiMn2O4) with a porous and hollow microspheric sructure has been successfully prepared with a facile method based on the complexation between Ni2+ and NH3. The obtained nanocomposite of 0.29 Mn2O3/0.14 NiMn2O4, expressed as Ni0.14Mn0.86O1.43, with nanometer-sized building blocks exhibits a high reversible capacity of 615 mA h g-1, which is about 90% of theoretical value at the current density of 800 mA h g-1, and long lifespan with retained capacities of 553 and 408 mA h g-1 after 150 cycles at 200 and 800 mA g-1, respectively, as an anode material for lithium-ion batteries.

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

    NASA Astrophysics Data System (ADS)

    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.

  15. [Preparation of anodic oxidation layer on the surface of pure titanium and its biological activity study].

    PubMed

    Gao, Shuchun; Zhai, Yuchun; Hu, Jinling

    2010-09-01

    This paper introduces how TiO2 film was prepared on pure titanium by anodic oxidation. Surface morphology and composition of the oxide film were analyzed by SEM coupled with EDAX. The deposition ability of hydroxyapatite of the anodized titanium in simulated body fluid (SBF) at 37 degrees C was evaluated. The results indicated that the oxide film was rough and honeycomb holes, connecting with each other, could be found on the surface. The holes with the diameter of 1-2 microm were distributed uniformly, which was typical for anodic oxidation. After alkaline treatment, hydroxyapatite deposition on the oxidized specimens in SBF was improved significantly. PMID:21179705

  16. Influence of sodium borate concentration on properties of anodic coatings obtained by micro arc oxidation on magnesium alloys

    NASA Astrophysics Data System (ADS)

    Zhang, R. F.; Zhang, S. F.; Shen, Y. L.; Zhang, L. H.; Liu, T. Z.; Zhang, Y. Q.; Guo, S. B.

    2012-06-01

    The influence of sodium borate concentration on the formation and properties of anodic coatings obtained by micro arc oxidation (MAO) on magnesium alloys was systematically studied in an alkaline solution with addition of 0-40 g/L sodium borate. It is shown that sodium borate can decrease the solution conductivity, take part in the coating formation and increase the coating thickness. With the increase of sodium borate concentration, the boron content in the coatings increases in the range of 10-20 g/L but decreases within the range of 20-40 g/L. Sodium borate cannot further improve the corrosion resistance attributed to the development of porous or rough anodic coatings.

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

    PubMed

    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

  18. Fabrication of silica moth-eye structures by photo-nanoimprinting using ordered anodic porous alumina molds

    NASA Astrophysics Data System (ADS)

    Yanagishita, Takashi; Endo, Takahide; Nishio, Kazuyuki; Masuda, Hideki

    2014-01-01

    Moth-eye structures composed of an ordered array of tapered SiO2 pillars were fabricated by photo-nanoimprinting using anodic porous alumina as a mold. The formation of SiO2 moth-eye structures was carried out using a photosensitive polysilane solution as a precursor of silica. The SiO2 moth-eye structures formed on the surface of a glass plate effectively suppressed the reflection of incident light.

  19. Nitrogen-doped porous carbon nanosheets as low-cost, high-performance anode material for sodium-ion batteries.

    PubMed

    Wang, Heng-guo; Wu, Zhong; Meng, Fan-lu; Ma, De-long; Huang, Xiao-lei; Wang, Li-min; Zhang, Xin-bo

    2013-01-01

    Between the sheets: Sodium-ion batteries are an attractive, low-cost alternative to lithium-ion batteries. Nitrogen-doped porous carbon sheets are prepared by chemical activation of polypyrrole-functionalized graphene sheets. When using the sheets as anode material in sodium-ion batteries, their unique compositional and structural features result in high reversible capacity, good cycling stability, and high rate capability. PMID:23225752

  20. Scalable synthesis of interconnected porous silicon/carbon composites by the Rochow reaction as high-performance anodes of lithium ion batteries.

    PubMed

    Zhang, Zailei; Wang, Yanhong; Ren, Wenfeng; Tan, Qiangqiang; Chen, Yunfa; Li, Hong; Zhong, Ziyi; Su, Fabing

    2014-05-12

    Despite the promising application of porous Si-based anodes in future Li ion batteries, the large-scale synthesis of these materials is still a great challenge. A scalable synthesis of porous Si materials is presented by the Rochow reaction, which is commonly used to produce organosilane monomers for synthesizing organosilane products in chemical industry. Commercial Si microparticles reacted with gas CH3 Cl over various Cu-based catalyst particles to substantially create macropores within the unreacted Si accompanying with carbon deposition to generate porous Si/C composites. Taking advantage of the interconnected porous structure and conductive carbon-coated layer after simple post treatment, these composites as anodes exhibit high reversible capacity and long cycle life. It is expected that by integrating the organosilane synthesis process and controlling reaction conditions, the manufacture of porous Si-based anodes on an industrial scale is highly possible. PMID:24700513

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

    PubMed

    Garcia-Segura, Sergi; Keller, Jürg; Brillas, Enric; Radjenovic, Jelena

    2015-01-01

    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. PMID:25464295

  2. Carbon-Confined SnO2-Electrodeposited Porous Carbon Nanofiber Composite as High-Capacity Sodium-Ion Battery Anode Material.

    PubMed

    Dirican, Mahmut; Lu, Yao; Ge, Yeqian; Yildiz, Ozkan; Zhang, Xiangwu

    2015-08-26

    Sodium resources are inexpensive and abundant, and hence, sodium-ion batteries are promising alternative to lithium-ion batteries. However, lower energy density and poor cycling stability of current sodium-ion batteries prevent their practical implementation for future smart power grid and stationary storage applications. Tin oxides (SnO2) can be potentially used as a high-capacity anode material for future sodium-ion batteries, and they have the advantages of high sodium storage capacity, high abundance, and low toxicity. However, SnO2-based anodes still cannot be used in practical sodium-ion batteries because they experience large volume changes during repetitive charge and discharge cycles. Such large volume changes lead to severe pulverization of the active material and loss of electrical contact between the SnO2 and carbon conductor, which in turn result in rapid capacity loss during cycling. Here, we introduce a new amorphous carbon-coated SnO2-electrodeposited porous carbon nanofiber (PCNF@SnO2@C) composite that not only has high sodium storage capability, but also maintains its structural integrity while ongoing repetitive cycles. Electrochemical results revealed that this SnO2-containing nanofiber composite anode had excellent electrochemical performance including high-capacity (374 mAh g(-1)), good capacity retention (82.7%), and large Coulombic efficiency (98.9% after 100th cycle). PMID:26252051

  3. Oxide-dispersion strengthening of porous powder metalurgy parts

    DOEpatents

    Judkins, Roddie R.

    2002-01-01

    Oxide dispersion strengthening of porous metal articles includes the incorporation of dispersoids of metallic oxides in elemental metal powder particles. Porous metal articles, such as filters, are fabricated using conventional techniques (extrusion, casting, isostatic pressing, etc.) of forming followed by sintering and heat treatments that induce recrystallization and grain growth within powder grains and across the sintered grain contact points. The result is so-called "oxide dispersion strengthening" which imparts, especially, large increases in creep (deformation under constant load) strength to the metal articles.

  4. Studies of porous anodic alumina using spin echo scattering angle measurement

    NASA Astrophysics Data System (ADS)

    Stonaha, Paul

    The properties of a neutron make it a useful tool for use in scattering experiments. We have developed a method, dubbed SESAME, in which specially designed magnetic fields encode the scattering signal of a neutron beam into the beam's average Larmor phase. A geometry is presented that delivers the correct Larmor phase (to first order), and it is shown that reasonable variations of the geometry do not significantly affect the net Larmor phase. The solenoids are designed using an analytic approximation. Comparison of this approximate function with finite element calculations and Hall probe measurements confirm its validity, allowing for fast computation of the magnetic fields. The coils were built and tested in-house on the NBL-4 instrument, a polarized neutron reflectometer whose construction is another major portion of this work. Neutron scattering experiments using the solenoids are presented, and the scattering signal from porous anodic alumina is investigated in detail. A model using the Born Approximation is developed and compared against the scattering measurements. Using the model, we define the necessary degree of alignment of such samples in a SESAME measurement, and we show how the signal retrieved using SESAME is sensitive to range of detectable momentum transfer.

  5. Study of fluid and transport properties of porous anodic aluminum membranes by dynamic atomic force microscopy.

    PubMed

    Wu, Chu; Leese, Hannah S; Mattia, Davide; Dagastine, Raymond R; Chan, Derek Y C; Tabor, Rico F

    2013-07-16

    Recent work on carbon nanotubes (CNT) has focused on their potential application in water treatment as a result of their predicted and observed enhanced flow rates. Recent work on the lesser-known porous anodic alumina membranes (PAAMs) has also shown flow enhancement, albeit at only a fraction of what has been observed in CNTs. Despite their potential applications, little research has been conducted on PAAMs' hydrodynamic properties, and in this Article we present experimental results and theoretical models that explore the fluid flow behavior around and through these membranes. The experiments were conducted using an atomic force microscope (AFM) that pushed a solid silica particle against PAAMs that were characterized with different pore diameters. Furthermore, the PAAMs were classified as either closed or open, with the latter allowing fluid to pass through. The theoretical model developed to describe the experimental data incorporates Derjaguin-Landau-Verwey-Overbeek (DLVO) effects, cantilever drag, and hydrodynamic forces. By using the slip boundary condition for the hydrodynamic forces, we were able to fit the model to experimental findings and also demonstrate that the difference between closed and open PAAMs was negligible. The slip lengths did not correspond to any physical feature of the PAAMs, but our model does provide a simple yet effective means of describing the hydrodynamics for not only PAAMs but for membranes in general. PMID:23750974

  6. Optical properties of ordered carbon nanotube arrays grown in porous anodic alumina templates.

    PubMed

    Zuidema, John; Ruan, Xiulin; Fisher, Timothy S

    2013-09-23

    We have synthesized ordered carbon nanotube (CNT) arrays in porous anodic alumina (PAA) matrix, and have characterized their total optical reflectance and bi-directional reflectance distribution function after each processing step of the microwave plasma chemical vapor deposition process (MPCVD). For a PAA sample without CNT growth, the reflectance shows an oscillating pattern with wavelength that agrees reasonably with a multilayer model. During the MPCVD process, heating the sample significantly reduces the reflectance by 30-40%, the plasma treatment reduces the reflectance by another 5-10%, and the CNT growth further reduces the reflectance by 2-3%. After an atomic layer deposition (ALD) process, the reflectance increases to the embedded CNT arrays. After etching and exposure of CNT tips, the reflectance almost returns to the original pattern with slightly higher reflectance. Bi-directional reflectance distribution function (BRDF) measurements show that the CNT-PAA surface is quite specular as indicated by a large lobe at the specular angle, while the secondary lobe can be attributed to surface roughness. PMID:24104097

  7. Thermally Engineered Blue Photoluminescence of Porous Anodic Alumina Membranes for Promising Optical Biosensors

    NASA Astrophysics Data System (ADS)

    Bu, Sang Don; Cho, Sam Yeon; Choi, Yong Chan; Kim, Jin Woo; Han, Jin Kyu; Kwak, Jin Ho; Yang, Sun A.

    Optical biosensors based on porous anodic alumina membranes (PAAMs) have shown to be an effective device because of their unique optical properties and biocompatibility. Among various optical properties, photoluminescence (PL) emission derived from PAAMs is one of the most suitable characteristics. However, the origin of PL from PAA is unclear and still in doubt. Therefore, it is essential for further potential practical applications to understand the origin of PL and PL variations. Here, we investigate the effects of post-annealing temperatures on the blue PL of amorphous PAAMs fabricated in oxalic acid. We find that the blue PL emission is strongly dependent on the thermal properties. A strong blue PL at a peak of ~460 nm is observed from the initial PAAM (not annealed PAAM) and this PL band can be divided into two Gaussian components at 458 ~ +/- ~ 4 nm (P1 band) and 517 ~ +/- 7nm (P2 band). As the temperature increases to 600 ° C , the intensities of two PL bands gradually increase. During temperature increases from 600 to 700 ° C , the P2 band increases but the P1 band decreases. The analyses of electron paramagnetic resonance, Fourier transform infrared spectroscopy, and ultraviolet-visible absorption spectroscopy show that the P1 and P2 bands originate from the unstable carboxylates and the stable carboxylates, respectively.

  8. Additional Electrochemical Treatment Effects on the Switching Characteristics of Anodic Porous Alumina Resistive Switching Memory

    NASA Astrophysics Data System (ADS)

    Otsuka, Shintaro; Takeda, Ryouta; Furuya, Saeko; Shimizu, Tomohiro; Shingubara, Shouso; Iwata, Nobuyuki; Watanabe, Tadataka; Takano, Yoshiki; Takase, Kouichi

    2012-06-01

    We have investigated the current-voltage characteristics of a resistive switching memory (ReRAM), especially the reproducibility of the switching voltage between an insulating state and a metallic state. The poor reproducibility hinders the practical use of this memory. According to a filament model, the variation of the switching voltage may be understood in terms of the random choice of filaments with different conductivities and lengths at each switching. A limitation of the number of conductive paths is expected to lead to the suppression of the variation of switching voltage. In this study, two strategies for the limitation have been proposed using an anodic porous alumina (APA). The first is the reduction of the number of conductive paths by restriction of the contact area between the top electrodes and the insulator. The second is the lowering of the resistivity of the insulator, which makes it possible to grow filaments with the same characteristics by electrochemical treatments using a pulse-electroplating technique.

  9. Ceria-Based Anodes for Next Generation Solid Oxide Fuel Cells

    NASA Astrophysics Data System (ADS)

    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

  10. Poly L-lysine (PLL)-mediated porous hematite clusters as anode materials for improved Li-ion batteries

    NASA Astrophysics Data System (ADS)

    Kim, Kun-Woo; Lee, Sang-Wha

    2015-09-01

    Porous hematite clusters were prepared as anode materials for improved Li-ion batteries. First, poly-L-lysine (PLL)-linked Fe3O4 was facilely prepared via cross-linking between the positive amine groups of PLL and carboxylate-bound Fe3O4. The subsequent calcination transformed the PLL-linked Fe3O4 into porous hematite clusters (Fe2O3@PLL) consisting of spherical α-Fe2O3 particles. Compared with standard Fe2O3, Fe3O4@PLL exhibited improved electrochemical performance as anode materials. The discharge capacity of Fe2O3@PLL was retained at 814.7 mAh g-1 after 30 cycles, which is equivalent to 80.4% of the second discharge capacity, whereas standard Fe2O3 exhibited a retention capacity of 352.3 mAh g-1. The improved electrochemical performance of Fe2O3@PLL was mainly attributed to the porous hematite clusters with mesoporosity (20-40 nm), which was beneficial for facilitating ion transport, suggesting a useful guideline for the design of porous architectures with higher retention capacity. [Figure not available: see fulltext.

  11. Porous carbon nanotubes decorated with nanosized cobalt ferrite as anode materials for high-performance lithium-ion batteries

    NASA Astrophysics Data System (ADS)

    Wang, Lingyan; Zhuo, Linhai; Cheng, Haiyang; Zhang, Chao; Zhao, Fengyu

    2015-06-01

    Generally, the fast ion/electron transport and structural stability dominate the superiority in lithium-storage applications. In this work, porous carbon nanotubes decorated with nanosized CoFe2O4 particles (p-CNTs@CFO) have been rationally designed and synthesized by the assistance of supercritical carbon dioxide (scCO2). When tested as anode materials for lithium-ion batteries, the p-CNTs@CFO composite exhibits outstanding electrochemical behavior with high lithium-storage capacity (1077 mAh g-1 after 100 cycles) and rate capability (694 mAh g-1 at 3 A g-1). These outstanding electrochemical performances are attributed to the synergistic effect of porous p-CNTs and nanosized CFO. Compared to pristine CNTs, the p-CNTs with substantial pores in the tubes possess largely increased specific surface area and rich oxygen-containing functional groups. The porous structure can not only accommodate the volume change during lithiation/delithiation processes, but also provide bicontinuous electron/ion pathways and large electrode/electrolyte interface, which facilitate the ion diffusion kinetics, improving the rate performance. Moreover, the CFO particles are bonded strongly to the p-CNTs through metal-oxygen bridges, which facilitate the electron fast capture from p-CNTs to CFO, and thus resulting in a high reversible capacity and excellent rate performance. Overall, the porous p-CNTs provide an efficient way for ion diffusion and continuous electron transport as anode materials.

  12. Micro-tubular solid oxide fuel cell based on a porous yttria-stabilized zirconia support

    PubMed Central

    Panthi, Dhruba; Tsutsumi, Atsushi

    2014-01-01

    Solid oxide fuel cells (SOFCs) are promising electrochemical energy conversion devices owing to their high power generation efficiency and environmentally benign operation. Micro-tubular SOFCs, which have diameters ranging from a few millimeters to the sub-millimeter scale, offer several advantages over competing SOFCs such as high volumetric power density, good endurance against thermal cycling, and flexible sealing between fuel and oxidant streams. Herein, we successfully realized a novel micro-tubular SOFC design based on a porous yttria-stabilized zirconia (YSZ) support using multi-step dip coating and co-sintering methods. The micro-tubular SOFC consisted of Ni-YSZ, YSZ, and strontium-doped lanthanum manganite (LSM)–YSZ as the anode, electrolyte, and cathode, respectively. In addition, to facilitate current collection from the anode and cathode, Ni and LSM were applied as an anode current collector and cathode current collector, respectively. Micro-crystalline cellulose was selected as a pore former to achieve better shrinkage behavior of the YSZ support so that the electrolyte layer could be densified at a co-sintering temperature of 1300°C. The developed micro-tubular design showed a promising electrochemical performance with maximum power densities of 525, 442, and 354 mW cm−2 at 850, 800, and 750°C, respectively. PMID:25169166

  13. Micro-tubular solid oxide fuel cell based on a porous yttria-stabilized zirconia support

    NASA Astrophysics Data System (ADS)

    Panthi, Dhruba; Tsutsumi, Atsushi

    2014-08-01

    Solid oxide fuel cells (SOFCs) are promising electrochemical energy conversion devices owing to their high power generation efficiency and environmentally benign operation. Micro-tubular SOFCs, which have diameters ranging from a few millimeters to the sub-millimeter scale, offer several advantages over competing SOFCs such as high volumetric power density, good endurance against thermal cycling, and flexible sealing between fuel and oxidant streams. Herein, we successfully realized a novel micro-tubular SOFC design based on a porous yttria-stabilized zirconia (YSZ) support using multi-step dip coating and co-sintering methods. The micro-tubular SOFC consisted of Ni-YSZ, YSZ, and strontium-doped lanthanum manganite (LSM)-YSZ as the anode, electrolyte, and cathode, respectively. In addition, to facilitate current collection from the anode and cathode, Ni and LSM were applied as an anode current collector and cathode current collector, respectively. Micro-crystalline cellulose was selected as a pore former to achieve better shrinkage behavior of the YSZ support so that the electrolyte layer could be densified at a co-sintering temperature of 1300°C. The developed micro-tubular design showed a promising electrochemical performance with maximum power densities of 525, 442, and 354 mW cm-2 at 850, 800, and 750°C, respectively.

  14. Porous Co{sub 3}O{sub 4} nanorods as anode for lithium-ion battery with excellent electrochemical performance

    SciTech Connect

    Guo, Jinxue; Chen, Lei; Zhang, Xiao Chen, Haoxin

    2014-05-01

    In this manuscript, porous Co{sub 3}O{sub 4} nanorods are prepared through a two-step approach which is composed of hydrothermal process and heating treatment as high performance anode for lithium-ion battery. Benefiting from the porous structure and 1-dimensional features, the product becomes robust and exhibits high reversible capability, good cycling performance, and excellent rate performance. - Graphical abstract: 1D porous Co{sub 3}O{sub 4} nanostructure as anode for lithium-ion battery with excellent electrochemical performance. - Highlights: • A two-step route has been applied to prepare 1D porous Co{sub 3}O{sub 4} nanostructure. • Its porous feature facilitates the fast transport of electron and lithium ion. • Its porous structure endows it with capacities higher than its theoretical capacity. • 1D nanostructure can tolerate volume changes during lithation/delithiation cycles. • It exhibits high capacity, good cyclability and excellent rate performance.

  15. Thermal investigation of an electrical high-current arc with porous gas-cooled anode

    NASA Technical Reports Server (NTRS)

    Eckert, E. R. G.; Schoeck, P. A.; Winter, E. R. F.

    1984-01-01

    The following guantities were measured on a high-intensity electric arc with tungsten cathode and transpiration-cooled graphite anode burning in argon: electric current and voltage, cooling gas flow rate (argon), surface temperature of the anode and of the anode holder, and temperature profile in three cross-sections of the arc are column. The last mentioned values were obtained from spectroscopic photographs. From the measured quantities, the following values were calculated: the heat flux into the anode surface, the heat loss of the anode by radiation and conduction, and the heat which was regeneratively transported by the cooling gas back into the arc space. Heat balances for the anode were also obtained. The anode losses (which are approximately 80% of the total arc power for free burning arcs) were reduced by transpiration cooling to 20%. The physical processes of the energy transfer from the arc to the anode are discussed qualitatively.

  16. Structural micro-porous carbon anode for rechargeable lithium-ion batteries

    DOEpatents

    Delnick, Frank M.; Even, Jr., William R.; Sylwester, Alan P.; Wang, James C. F.; Zifer, Thomas

    1995-01-01

    A secondary battery having a rechargeable lithium-containing anode, a cathode and a separator positioned between the cathode and anode with an organic electrolyte solution absorbed therein is provided. The anode comprises three-dimensional microporous carbon structures synthesized from polymeric high internal phase emulsions or materials derived from this emulsion source, i.e., granules, powders, etc.

  17. Structural micro-porous carbon anode for rechargeable lithium-ion batteries

    DOEpatents

    Delnick, F.M.; Even, W.R. Jr.; Sylwester, A.P.; Wang, J.C.F.; Zifer, T.

    1995-06-20

    A secondary battery having a rechargeable lithium-containing anode, a cathode and a separator positioned between the cathode and anode with an organic electrolyte solution absorbed therein is provided. The anode comprises three-dimensional microporous carbon structures synthesized from polymeric high internal phase emulsions or materials derived from this emulsion source, i.e., granules, powders, etc. 6 figs.

  18. Anodic Aluminum Oxide (AAO) Membranes for Cellular Devices

    NASA Astrophysics Data System (ADS)

    Ventura, Anthony P.

    Anodic Aluminum Oxide (AAO) membranes can be fabricated with a highly tunable pore structure making them a suitable candidate for cellular hybrid devices with single-molecule selectivity. The objective of this study was to characterize the cellular response of AAO membranes with varying pore sizes to serve as a proof-of-concept for an artificial material/cell synapse system. AAO membranes with pore diameters ranging from 34-117 nm were achieved via anodization at a temperature of -1°C in a 2.7% oxalic acid electrolyte. An operating window was established for this setup to create membranes with through-pore and disordered pore morphologies. C17.2 neural stem cells were seeded onto the membranes and differentiated via serum withdrawal. The data suggests a highly tunable correlation between AAO pore diameter and differentiated cell populations. Analysis of membranes before and after cell culture indicated no breakdown of the through-pore structure. Immunocytochemistry (ICC) showed that AAO membranes had increased neurite outgrowth when compared to tissue culture treated (TCT) glass, and neurite outgrowth varied with pore diameter. Additionally, lower neuronal percentages were found on AAO as compared to TCT glass; however, neuronal population was also found to vary with pore diameter. Scanning electron microscopy (SEM) and ICC images suggested the presence of a tissue-like layer with a mixed-phenotype population. AAO membranes appear to be an excellent candidate for cellular devices, but more work must be completed to understand the surface chemistry of the AAO membranes as it relates to cellular response.

  19. Transition metal oxide as anode interface buffer for impedance spectroscopy

    NASA Astrophysics Data System (ADS)

    Xu, Hui; Tang, Chao; Wang, Xu-Liang; Zhai, Wen-Juan; Liu, Rui-Lan; Rong, Zhou; Pang, Zong-Qiang; Jiang, Bing; Fan, Qu-Li; Huang, Wei

    2015-12-01

    Impedance spectroscopy is a strong method in electric measurement, which also shows powerful function in research of carrier dynamics in organic semiconductors when suitable mathematical physical models are used. Apart from this, another requirement is that the contact interface between the electrode and materials should at least be quasi-ohmic contact. So in this report, three different transitional metal oxides, V2O5, MoO3 and WO3 were used as hole injection buffer for interface of ITO/NPB. Through the impedance spectroscopy and PSO algorithm, the carrier mobilities and I-V characteristics of the NPB in different devices were measured. Then the data curves were compared with the single layer device without the interface layer in order to investigate the influence of transitional metal oxides on the carrier mobility. The careful research showed that when the work function (WF) of the buffer material was just between the work function of anode and the HOMO of the organic material, such interface material could work as a good bridge for carrier injection. Under such condition, the carrier mobility measured through impedance spectroscopy should be close to the intrinsic value. Considering that the HOMO (or LUMO) of most organic semiconductors did not match with the work function of the electrode, this report also provides a method for wide application of impedance spectroscopy to the research of carrier dynamics.

  20. Structure of triglycine sulfate embedded in porous aluminum oxide

    NASA Astrophysics Data System (ADS)

    Golitsyna, O. M.; Drozhdin, S. N.; Zanin, I. E.; Gridnev, A. E.

    2012-11-01

    The X-ray diffraction investigations have been performed for nanocomposite materials based on porous aluminum oxide with inclusions of TGS and TGS, which is doped with L,α-alanine (ATGS). The presence of the TGS and ATGS textures in pores of Al2O3 films has been found. It has been established that, under conditions of confined geometry, the broadening of diffraction maxima of the reflection is caused by the size effect. The temperature dependences of the order parameter for porous aluminum oxide with TGS inclusions have been constructed.

  1. Porous tungsten oxide nanoflakes for highly alcohol sensitive performance

    NASA Astrophysics Data System (ADS)

    Xiao, J.; Liu, P.; Liang, Y.; Li, H. B.; Yang, G. W.

    2012-10-01

    Porous tungsten oxide (WO3) nanoflakes have been synthesized by a simple and green approach in an ambient environment. As a precursor solution a polycrystalline hydrated tungstite (H2WO4.H2O) nanoparticles colloid was first prepared by pulsed-laser ablation of a tungsten target in water. The H2WO4.H2O nanoflakes were produced by 72 h aging treatment at room temperature. Finally, porous WO3 nanoflakes were synthesized by annealing at 800 °C for 4 h. Considering the large surface-to-volume ratio of porous nanoflakes, a porous WO3 nanoflake gas sensor was fabricated, which exhibits an excellent sensor response performance to alcohol concentrations in the range of 20 to 600 ppm under low working temperature. This high response was attributed to the highly crystalline and porous flake-like morphology, which leads to effective adsorption and desorption, and provides more active sites for the gas molecules' reaction. These findings showed that the porous tungsten oxide nanoflake has great potential in gas-sensing performance.

  2. Numerical Simulation of Capillary Channels Growth in Heterogeneous Porous Anode in Aluminum Electrolysis Cells by Lattice Boltzmann Method

    NASA Astrophysics Data System (ADS)

    Diop, Mouhamadou; Wang, Moran

    2014-11-01

    This paper presents results obtained from three-dimensional numerical simulations of multiphase reactive flows in porous anode block in aluminum cells controlling a great extent of mass, heat and chemical balance in the anode-cathode region. A lattice Boltzmann method based on thermal reactive multiphase flows, is developed to simulate the spatial and temporal distribution of fluids, the effects of gas rate and capillary instabilities in the cryolite. A new model, which involves eighteen lattice particles for the first and second derivative, is proposed to achieve accurate simulations at high fluid density ratio. The effects of the dissolution of gas and the capillary number on the flow field induced by gas bubbles evolution are investigated. It is found that capillary channels in the limit of small Stefan, the radial transport of reactant out of the capillary channel decay exponentially with the height of penetration in the porous anode. Several examples are solved by the proposed method to demonstrate the accuracy and robustness of the method.

  3. Nanomechanical humidity detection through porous alumina cantilevers

    PubMed Central

    Klimenko, Alexey; Lebedev, Vasiliy; Lukashin, Alexey; Eliseev, Andrey

    2015-01-01

    Summary We present here the behavior of the resonance frequency of porous anodic alumina cantilever arrays during water vapor adsorption and emphasize their possible use in the micromechanical sensing of humidity levels at least in the range of 10–22%. The sensitivity of porous anodic aluminium oxide cantilevers (Δf/Δm) and the humidity sensitivity equal about 56 Hz/pg and about 100 Hz/%, respectively. The approach presented here for the design of anodic alumina cantilever arrays by the combination of anodic oxidation and photolithography enables easy control over porosity, surface area, geometric and mechanical characteristics of the cantilever arrays for micromechanical sensing. PMID:26199836

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

    DOEpatents

    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.

  5. Hollow Porous SiO2 Nanocubes Towards High-performance Anodes for Lithium-ion Batteries

    PubMed Central

    Yan, Nan; Wang, Fang; Zhong, Hao; Li, Yan; Wang, Yu; Hu, Lin; Chen, Qianwang

    2013-01-01

    The high theoretical capacity and low discharge potential of silicon have attracted much attention on Si-based anodes. Herein, hollow porous SiO2 nanocubes have been prepared via a two-step hard-template process and evaluated as electrode materials for lithium-ion batteries. The hollow porous SiO2 nanocubes exhibited a reversible capacity of 919 mAhg−1 over 30 cycles. The reasonable property could be attributed to the unique hollow nanostructure with large volume interior and numerous crevices in the shell, which could accommodate the volume change and alleviate the structural strain during Li ions' insertion and extraction, as well as allow rapid access of Li ions during charge/discharge cycling. It is found that the formation of irreversible or reversible lithium silicates in the anodes determines the capacity of a deep-cycle battery, fast transportation of Li ions in hollow porous SiO2 nanocubes is beneficial to the formation of Li2O and Si, contributing to the high reversible capacity. PMID:23535780

  6. Photoluminescence emission of nanoporous anodic aluminum oxide films prepared in phosphoric acid

    PubMed Central

    2012-01-01

    The photoluminescence emission of nanoporous anodic aluminum oxide films formed in phosphoric acid is studied in order to explore their defect-based subband electronic structure. Different excitation wavelengths are used to identify most of the details of the subband states. The films are produced under different anodizing conditions to optimize their emission in the visible range. Scanning electron microscopy investigations confirm pore formation in the produced layers. Gaussian analysis of the emission data indicates that subband states change with anodizing parameters, and various point defects can be formed both in the bulk and on the surface of these nanoporous layers during anodizing. PMID:23272786

  7. Photoluminescence emission of nanoporous anodic aluminum oxide films prepared in phosphoric acid.

    PubMed

    Nourmohammadi, Abolghasem; Asadabadi, Saeid Jalali; Yousefi, Mohammad Hasan; Ghasemzadeh, Majid

    2012-01-01

    The photoluminescence emission of nanoporous anodic aluminum oxide films formed in phosphoric acid is studied in order to explore their defect-based subband electronic structure. Different excitation wavelengths are used to identify most of the details of the subband states. The films are produced under different anodizing conditions to optimize their emission in the visible range. Scanning electron microscopy investigations confirm pore formation in the produced layers. Gaussian analysis of the emission data indicates that subband states change with anodizing parameters, and various point defects can be formed both in the bulk and on the surface of these nanoporous layers during anodizing. PMID:23272786

  8. Photoluminescence emission of nanoporous anodic aluminum oxide films prepared in phosphoric acid

    NASA Astrophysics Data System (ADS)

    Nourmohammadi, Abolghasem; Asadabadi, Saeid Jalali; Yousefi, Mohammad Hasan; Ghasemzadeh, Majid

    2012-12-01

    The photoluminescence emission of nanoporous anodic aluminum oxide films formed in phosphoric acid is studied in order to explore their defect-based subband electronic structure. Different excitation wavelengths are used to identify most of the details of the subband states. The films are produced under different anodizing conditions to optimize their emission in the visible range. Scanning electron microscopy investigations confirm pore formation in the produced layers. Gaussian analysis of the emission data indicates that subband states change with anodizing parameters, and various point defects can be formed both in the bulk and on the surface of these nanoporous layers during anodizing.

  9. Gasoline-fueled solid oxide fuel cell using MoO2-Based Anode

    NASA Astrophysics Data System (ADS)

    Hou, Xiaoxue; Marin-Flores, Oscar; Kwon, Byeong Wan; Kim, Jinsoo; Norton, M. Grant; Ha, Su

    2014-12-01

    This short communication describes the performance of a solid oxide fuel cell (SOFC) fueled by directly feeding premium gasoline to the anode without using external reforming. The novel component of the fuel cell that enables such operation is the mixed conductivity of MoO2-based anode. Using this anode, a fuel cell demonstrating a maximum power density of 31 mW/cm2 at 0.45 V was successfully fabricated. Over a 24 h period of operation, the open cell voltage remained stable at ∼0.92 V. Scanning electron microscopy (SEM) examination of the anode surface pre- and post-testing showed no evidence of coking.

  10. Characterization of 430L porous supports obtained by powder extrusion moulding for their application in solid oxide fuel cells

    SciTech Connect

    Sotomayor, María Eugenia Ospina, Liliana María Levenfeld, Belén Várez, Alejandro

    2013-12-15

    The characterization of 430L stainless steel planar porous supports obtained by powder extrusion moulding was performed in this work. A thermoplastic multicomponent binder based on high density polyethylene and paraffin wax was selected for the process. Green supports were shaped by extrusion moulding, and subsequently the binder was removed by a thermal cycle previously optimized. Sintering was carried out at different temperatures in low vacuum. Density of sintered parts was measured by Archimedes' method and porosity was also evaluated through a microstructural analysis by optical microscopy. The porosity degree of samples sintered at low temperature was close to 35% which is a very suitable value for their application in SOFCs. Tensile tests were carried out in order to determine mechanical strength as a function of porosity degree. Based on these results, the best feedstock composition and processing parameters were selected. The oxidation behaviour in static air at high temperature was studied, and formed oxides were characterized in a scanning electron microscope equipped with energy dispersive analysis of X-rays. X-ray diffraction experiments were performed in order to identify the formed oxides based on formula Fe{sub 2−x}Cr{sub x}O{sub 3}. The results of these studies showed that this kind of ferritic stainless steel would be more suitable to be used as anodic supports where a rich hydrogen atmosphere is employed. Preliminary deposition tests allowed obtaining a homogeneous Ni–YSZ anode layer with a thickness of 10 μm on the porous metallic substrates. - Highlights: • 430L stainless steel porous supports were obtained by powder extrusion moulding. • Porosity degree was controlled sintering at different temperatures in low vacuum. • Tensile tests allowed determining mechanical strength of porous supports. • A study about its oxidation behaviour in static air at high temperature was realized. • After oxidation, formed oxides were

  11. Electrochemical performance of a solid oxide fuel cell with an anode based on Cu-Ni/CeO2 for methane direct oxidation

    NASA Astrophysics Data System (ADS)

    Hornés, Aitor; Escudero, María J.; Daza, Loreto; Martínez-Arias, Arturo

    2014-03-01

    A CuNi-CeO2/YSZ/LSF solid oxide fuel cell has been fabricated and tested with respect to its electrochemical activity for direct oxidation of dry methane. The electrodes have been prepared by impregnation of corresponding porous YSZ layers, using reverse microemulsions as impregnating medium for the anode (constituted by Cu-Ni at 1:1 atomic ratio in combination with CeO2). On the basis of I-V electrochemical testing complemented by impedance spectroscopy (IS) measurements it is shown the ability of the SOFC for direct oxidation of methane in a rather stable way. Differences in the behavior as a function of operating temperature (1023-1073 K) are also revealed and examined on the basis of analysis of IS spectra.

  12. Theoretical analysis of hydrogen oxidation reaction in solid oxide fuel cell anode based on species territory adsorption model

    NASA Astrophysics Data System (ADS)

    Nagasawa, Tsuyoshi; Hanamura, Katsunori

    2015-09-01

    A modified reaction model of hydrogen oxidation around a triple phase boundary (TPB) is proposed for solid oxide fuel cells (SOFCs) with a Ni/oxide ion conductor cermet anode containing proton conductor particles in order to describe the mechanism of anode overpotential reduction. In this model, three kinds of TPBs consisting of nickel metal, oxide ion conductors, proton conductors, and gas phases were considered. It was assumed that the chemical species could be adsorbed within a finite narrow area on each material around the TPB. The reaction rate in the anode was controlled by the surface reaction between the adsorbed hydrogen and adsorbed oxygen; all other reactions took place under chemical equilibrium. Based on the reaction model, analytical expressions of current density with oxygen activity and anode overpotential with current density could be obtained. The latter could combine the anode overpotential at low- and high-current-density regions, which were conventionally expressed independently. The analytical results were in good agreement with the experimental results for both the conventional anode and the new anode incorporating a proton conductor. Especially, the anode overpotential reduction could be explained by the additional supply of adsorbed hydrogen from the proton conductor to the TPB.

  13. Enhancement of direct urea-hydrogen peroxide fuel cell performance by three-dimensional porous nickel-cobalt anode

    NASA Astrophysics Data System (ADS)

    Guo, Fen; Cao, Dianxue; Du, Mengmeng; Ye, Ke; Wang, Guiling; Zhang, Wenping; Gao, Yinyi; Cheng, Kui

    2016-03-01

    A novel three-dimensional (3D) porous nickel-cobalt (Ni-Co) film on nickel foam is successfully prepared and further used as an efficient anode for direct urea-hydrogen peroxide fuel cell (DUHPFC). By varying the cobalt/nickel mole ratios into 0%, 20%, 50%, 80% and 100%, the optimized Ni-Co/Ni foam anode with a ratio of 80% is obtained in terms of the best cell performance among five anodes. Effects of the KOH and urea concentrations, the flow rate and operation temperature on the fuel cell performance are investigated. Results show DUHPFC with the 3D Ni-Co/Ni foam anode exhibits a higher performance than those reported direct urea fuel cells. The cell gives an open circuit voltage of 0.83 V and a peak power density as high as 17.4 and 31.5 mW cm-2 at 20 °C and 70 °C, respectively, when operating on 7.0 mol L-1 KOH and 0.5 mol L-1 urea as the fuel at a flow rate of 15 mL min-1. Besides, when the human urine is directly fed as the fuel, direct urine-hydrogen peroxide fuel cell reaches a maximum power density of 7.5 mW cm-2 with an open circuit voltage of 0.80 V at 20 °C, showing a good application prospect in wastewater treatment.

  14. An unexpected large capacity of ultrafine manganese oxide as a sodium-ion battery anode

    NASA Astrophysics Data System (ADS)

    Weng, Yu-Ting; Huang, Tzu-Yang; Lim, Chek-Hai; Shao, Pei-Sian; Hy, Sunny; Kuo, Chao-Yen; Cheng, Ju-Hsiang; Hwang, Bing-Joe; Lee, Jyh-Fu; Wu, Nae-Lih

    2015-11-01

    MnO2 is shown for the first time to be electrochemically active as a conversion anode for Na-ion batteries (NIBs). Space-confined ultrafine (UF)-MnO2, with an average crystal size of 4 nm, synthesized using a porous silicon dioxide templated hydrothermal process exhibits a high reversible sodiation capacity of 567 mA h g-1, in contrast to the negligible activity shown by the aggregates of larger (14 nm) MnO2 nanocrystallites. The remarkably enhanced sodiation activity of the UF-MnO2 is attributable to its greatly reduced crystal size, which facilitates diffusion of Na ions, along with high surface energy arising from extensive heterogeneous interfacial bonding with the SiO2 surrounding. The UF-MnO2 anode exhibits an exceptional rate and cycle performance, exhibiting >70% capacity retention after 500 cycles. In operando synchrotron X-ray absorption near-edge structural analysis reveals combined charge-storage mechanisms involving conversion reaction between Mn(iii) and Mn(ii) oxides, Mn(iii)-O1.5 + Na+ + e-- <--> 1/2Na2O + Mn(ii)-O, and non-Mn-centered redox reactions. The finding suggests a new strategy for ``activating'' the potential electrochemical electrode materials that appear inactive in the bulk form.MnO2 is shown for the first time to be electrochemically active as a conversion anode for Na-ion batteries (NIBs). Space-confined ultrafine (UF)-MnO2, with an average crystal size of 4 nm, synthesized using a porous silicon dioxide templated hydrothermal process exhibits a high reversible sodiation capacity of 567 mA h g-1, in contrast to the negligible activity shown by the aggregates of larger (14 nm) MnO2 nanocrystallites. The remarkably enhanced sodiation activity of the UF-MnO2 is attributable to its greatly reduced crystal size, which facilitates diffusion of Na ions, along with high surface energy arising from extensive heterogeneous interfacial bonding with the SiO2 surrounding. The UF-MnO2 anode exhibits an exceptional rate and cycle performance

  15. Study on degradation of solid oxide fuel cell anode by using pure nickel electrode

    NASA Astrophysics Data System (ADS)

    Jiao, Zhenjun; Shikazono, Naoki; Kasagi, Nobuhide

    2011-10-01

    In this study, the interactions between Ni and YSZ in solid oxide fuel cell anode and the influence of glass seal to anode performances have been investigated by pure Ni anode sintered on YSZ pellet. The evolution of Ni-YSZ interface in 100 h galvanostatic polarization in hydrogen is studied with different humidities in hydrogen. Electrochemical impedance spectroscopy was applied to analyze the time variation of the anode electrochemical characteristics. The interface microstructural changes were characterized by scanning electron microscopy. The influence of bulk gas humidity, gas-sealing material and Ni coarsening on anode durability was studied. The degradation of pure Ni anode is considered to be determined by the competition among the mechanisms of silicon deposition, YSZ interface morphological change and Ni coarsening.

  16. Preparation and application of a titanium dioxide/graphene oxide anode material for lithium-ion batteries

    NASA Astrophysics Data System (ADS)

    Siwińska-Stefańska, Katarzyna; Kurc, Beata

    2015-12-01

    This paper describes the synthesis and physicochemical properties of a new type of titania/graphene oxide (TA/GO) composite. Titania powder was synthesized via the sol-gel method, and its surface was functionalized with N-2-(aminoethyl)-3-aminopropyltrimethoxysilane (AAPTS) to increase its adhesion to graphene oxide. Transmission electron microscopy (TEM), non-invasive back scattering (NIBS), porous structure parameters (low-temperature nitrogen sorption), degree of modification of titania and TA/GO determined by Fourier-transform infrared spectroscopy (FT-IR), impedance analysis, charging/discharging and cyclic voltammetry were carried out. At a current density of 50 mA g-1, the good cyclability exhibited by the TA/GO anode can be readily retained at 370 mAh g-1 after 50 cycles, which is outstanding among the TiO2 composites reported in the literature.

  17. Bismuth Oxide: A New Lithium-Ion Battery Anode

    PubMed Central

    Li, Yuling; Trujillo, Matthias A.; Fu, Engang; Patterson, Brian; Fei, Ling; Xu, Yun; Deng, Shuguang; Smirnov, Sergei; Luo, Hongmei

    2013-01-01

    Bismuth oxide directly grown on nickel foam (p-Bi2O3/Ni) was prepared by a facile polymer-assisted solution approach and was used directly as a lithium-ion battery anode for the first time. The Bi2O3 particles were covered with thin carbon layers, forming network-like sheets on the surface of the Ni foam. The binder-free p-Bi2O3/Ni shows superior electrochemical properties with a capacity of 668 mAh/g at a current density of 800 mA/g, which is much higher than that of commercial Bi2O3 powder (c-Bi2O3) and Bi2O3 powder prepared by the polymer-assisted solution method (p-Bi2O3). The good performance of p-Bi2O3/Ni can be attributed to higher volumetric utilization efficiency, better connection of active materials to the current collector, and shorter lithium ion diffusion path. PMID:24416506

  18. Luminescence of europium-doped anode oxide films on titanium-aluminum composites

    NASA Astrophysics Data System (ADS)

    Sokol, V. A.; Pinaeva, M. M.; Gurskaya, E. A.; Stekol'Nikov, A. A.

    2000-03-01

    The luminescence of europium in anode oxide films (AOF) on titanium-aluminum film composites is investigated. It is shown that the intensity distribution in the continuous and line luminescence spectra of europium introduced into the AOF directly in the process of anodic oxidation essentially depends on the sequence of arrangement of the layers of metal films and on the temperature of their heat treatment preceding the process of anodic oxidation. It is established that the nature of the luminescence spectrum of the AOF correlates with the chronovoltammetry diagrams of anodic oxidation. Composites with a high degree of europium doping are found and methods of searching for composites for creating new materials of electronic technology are outlined.

  19. Anode shroud for off-gas capture and removal from electrolytic oxide reduction system

    SciTech Connect

    Bailey, James L.; Barnes, Laurel A.; Wiedmeyer, Stanley G.; Williamson, Mark A.; Willit, James L.

    2014-07-08

    An electrolytic oxide reduction system according to a non-limiting embodiment of the present invention may include a plurality of anode assemblies and an anode shroud for each of the anode assemblies. The anode shroud may be used to dilute, cool, and/or remove off-gas from the electrolytic oxide reduction system. The anode shroud may include a body portion having a tapered upper section that includes an apex. The body portion may have an inner wall that defines an off-gas collection cavity. A chimney structure may extend from the apex of the upper section and be connected to the off-gas collection cavity of the body portion. The chimney structure may include an inner tube within an outer tube. Accordingly, a sweep gas/cooling gas may be supplied down the annular space between the inner and outer tubes, while the off-gas may be removed through an exit path defined by the inner tube.

  20. Growth and Filling Regularities of Filamentary Channels in Non-Metallic Inorganic Coatings Under Anodic Oxidation of Valve Metals. Mathematical Modeling

    NASA Astrophysics Data System (ADS)

    Mamaev, A. I.; Mamaeva, V. A.; Kolenchin, N. F.; Chubenko, A. K.; Kovalskaya, Ya. B.; Dolgova, Yu. N.; Beletskaya, E. Yu.

    2015-12-01

    Theoretical models are developed for growth and filling processes in filamentary channels of nanostructured non-metallic coatings produced by anodizing and microplasma oxidation. Graphical concentration distributions are obtained for channel-reacting anions, cations, and sparingly soluble reaction products depending on the time of electric current transmission and the length of the filamentary channel. Graphical distributions of the front moving velocity for the sparingly soluble compound are presented. The resulting model representation increases the understanding of the anodic process nature and can be used for a description and prediction of porous anodic film growth and filling. It is shown that the character of the filamentary channel growth and filling causes a variety of processes determining the textured metal - nonmetallic inorganic coating phase boundary formation.

  1. On-demand supply of slurry fuels to a porous anode of a direct carbon fuel cell: Attempts to increase fuel-anode contact and realize long-term operation

    NASA Astrophysics Data System (ADS)

    Li, Chengguo; Yi, Hakgyu; Lee, Donggeun

    2016-03-01

    In this paper, we propose a novel idea that might allow resolution of the two biggest challenges that hinder practical use of direct carbon fuel cells (DCFC). This work involved 1) the use of three types of porous Ni anode with different pore sizes, 2) size matching between the anode pores and solid fuel particles in a molten-carbonate (MC) slurry, and 3) provision of a continuous supply of fuel-MC slurry through the porous Ni anode. As a result, larger numbers of smaller pores in the anode were preferred for extending the triple phase boundary (TPB), as long as the fuel particles were sufficiently small to have full access to the inner pore spaces of the anode. For example, the maximal power density achieved in the case of optimal size matching, reached 645 mW cm-2, which is 14-times greater than that for the case of poorest size-matching and 64-times larger than that for a non-porous anode, and lasted for more than 20 h. After 20 h of steady operation at a fixed current density (700 mA cm-2), the electric potential slightly decreased due to partial consumption of the fuel. The cell performance readily recovered after restarting the supply of MC-fuel slurry.

  2. Vertical devices from single-walled carbon nanotubes templated in porous anodic alumina

    NASA Astrophysics Data System (ADS)

    Franklin, Aaron D.

    Over the past decade, tremendous progress has been realized in the fabrication and characterization of single-walled carbon nanotube (CNT) electronic devices. For example, with advantages such as ballistic transport and the absence of surface states, CNTs have been proposed as an ideal 1D channel material for next generation field-effect transistors (FETs). However, the literature is replete with reports of individual high-performance devices that lack the demonstration or feasibility of being fabricated at a large scale. One of the primary obstacles to fabricating highly integrated CNT devices is the placement of the nanotubes at a defined spacing and in precise locations. Nearly all CNT devices to date have been configured in a planar geometry (with the CNT supported horizontally on a substrate) and have primarily relied on random processes for dispersing/growing and contacting the CNTs. Ideally, a high-performance CNTFET would consist of multiple, densely packed CNTs that are aligned, having surround gates, low-barrier contacts, and a sub-100 nm channel length. Such multi-nanotube CNTFETs should further be fabricated in a manner that can be scaled for high-level integration and that is compatible with modern CMOS processing. This dissertation describes the development of a platform based on vertically aligned CNTs templated in porous anodic alumina (PAA) for the scalable fabrication of multi-nanotube CNTFETs with surround gates as well as several other nanoelectronic devices. PAA is a template consisting of hexagonally ordered pores that result from the anodization of an Al film. By embedding a catalyst layer within PAA, single-walled CNTs are synthesized from the nanoscale vertical pores (pore diameter ≈20 nm, spacing ≈100 nm) at a yield of no more than one nanotube per pore. After synthesis, the CNTs are contacted within the pores by electrodepositing Pd, a known low-barrier contact metal for CNTs, to form nanowires that electrically address the CNTs near

  3. Fabrication and characterization of all-ceramic solid oxide fuel cells based on composite oxide anode

    NASA Astrophysics Data System (ADS)

    Kim, Jeonghee; Shin, Dongwook; Son, Ji-Won; Lee, Jong-Ho; Kim, Byung-Kook; Je, Hae-June; Lee, Hae-Weon; Yoon, Kyung Joong

    2013-11-01

    All-ceramic solid oxide fuel cells (SOFCs), which offer advantages in carbon tolerance, sulfur resistance and redox stability, are fabricated and evaluated. The electrolyte-supported cells are composed of a La0.75Sr0.25Cr0.5Mn0.5O3-δ (LSCM)-Ce0.9Gd0.1O1.95-δ (GDC) anode, an Y2O3-stabilized ZrO2 (YSZ) electrolyte, a GDC interdiffusion barrier layer, and a La0.8Sr0.2Co0.2Fe0.8O3-δ (LSCF)-GDC cathode. A particle-dispersed glycine-nitrate process is developed to synthesize extremely fine and homogeneous LSCM-GDC ceramic composite powders. The electrochemical performance of the LSCM-GDC anode is comparable to that of conventional Ni-based anodes. The impedance spectra of the all-ceramic SOFCs are successfully interpreted by the independent characterization of the individual electrodes via half-cell measurements. The impedance of the LSCM-GDC anode is dominated by a low-frequency arc originating from the “chemical capacitance”, which is associated with the variation of the oxygen nonstoichiometry in the mixed conducting ceramic electrode. In addition, the impedance arc associated with the electrode-gas interaction is observed in the LSCM-GDC anode. The rate-limiting processes for the LSCF-GDC cathode are observed to be solid-state oxygen diffusion and surface chemical exchange. Herein, the reaction mechanisms and rate-limiting processes of the all-ceramic SOFCs are discussed in detail and compared with those of conventional Ni-based SOFCs.

  4. Interpreting the shock response of porous oxide systems

    NASA Astrophysics Data System (ADS)

    Fredenburg, David; Koller, Darcie

    2013-06-01

    Oxide powders subjected to varying levels of shock loading can exhibit a complex response that differs significantly from that which is commonly observed in metals. As much of the early model development for particulates has been focused on metallic systems, the current state of the art in compaction and equation of state modeling is often unable to capture the wide range of compression responses observed in porous oxides. Specifically, the possibility of polymorphic phase transformations requires additional considerations in the development of compaction and equation of state models for these systems. In the present work, the shock response of several porous oxide systems is critically examined with respect to the equilibrium phase boundaries to identify the existence and extent of transformations under shock loading, and the influence of intrinsic and extrinsic properties on the onset of transformation.

  5. Growth of porous anodized alumina on the sputtered aluminum films with 2D-3D morphology for high specific surface area

    NASA Astrophysics Data System (ADS)

    Liao, M. W.; Chung, C. K.

    2014-08-01

    The porous anodic aluminum oxide (AAO) with high-aspect-ratio pore channels is widely used as a template for fabricating nanowires or other one-dimensional (1D) nanostructures. The high specific surface area of AAO can also be applied to the super capacitor and the supporting substrate for catalysis. The rough surface could be helpful to enhance specific surface area but it generally results in electrical field concentration even to ruin AAO. In this article, the aluminum (Al) films with the varied 2D-3D morphology on Si substrates were prepared using magnetron sputtering at a power of 50 W-185 W for 1 h at a working pressure of 2.5 × 10-1 Pa. Then, AAO was fabricated from the different Al films by means of one-step hybrid pulse anodizing (HPA) between the positive 40 V and the negative -2 V (1 s:1 s) for 3 min in 0.3 M oxalic acid at a room temperature. The microstructure and morphology of Al films were characterized by X-ray diffraction, scanning electron microscope and atomic force microscope, respectively. Some hillocks formed at the high target power could be attributed to the grain texture growth in the normal orientation of Al(1 1 1). The 3D porous AAO structure which is different from the conventional 2D planar one has been successfully demonstrated using HPA on the film with greatly rough hillock-surface formed at the highest power of 185 W. It offers a potential application of the new 3D AAO to high specific surface area devices.

  6. Quantitative analysis methods for three-dimensional microstructure of the solid-oxide fuel cell anode

    NASA Astrophysics Data System (ADS)

    Song, X.; Guan, Y.; Liu, G.; Chen, L.; Xiong, Y.; Zhang, X.; Tian, Y.

    2013-10-01

    The electrochemical performance is closely related to three-dimensional microstructure of the Ni-YSZ anode. X-ray nano-tomography combined with quantitative analysis methods has been applied to non-destructively study the internal microstructure of the porous Ni-YSZ anode. In this paper, the methods for calculating some critical structural parameters, such as phase volume fraction, connectivity and active triple phase boundary (TPB) density were demonstrated. These structural parameters help us to optimize electrodes and improve the performance.

  7. Conductive polycrystalline diamond probes for local anodic oxidation lithography

    NASA Astrophysics Data System (ADS)

    Ulrich, A. J.; Radadia, A. D.

    2015-11-01

    This is the first report characterizing local anodic oxidation (LAO) lithography performed using conductive monolithic polycrystalline diamond (MD) and conductive polycrystalline diamond-coated (DC) tips and comparing it to the diamond-like carbon-coated and metal-coated silicon tips. The range and the rate of increase in the lithographic linewidth and height with tip bias (dw/dV and dh/dV) differed based on the tip material. The DC tips resulted in wider and taller lines and a higher dw/dV and dh/dV compared to metal-coated tips with a similar force constant (k Avg). The metal-coated and the DC tips with comparable k Avg showed comparable threshold voltages, whereas the MD tips with similar k Avg showed a higher threshold voltage. The MD tips exhibited less than half the height and nearly half the dw/dV and dh/dV obtained with the metal-coated tips with similar k Avg, thus also resulting in a smaller width at -10 V. The linewidths were found to be proportional to the inverse of the log of write speed (v) for all the tips; however, the proportionality constant varied with tip material; the DC tips had larger values, and the MD and the metal-coated tips had comparable values. When varying the speed, the height was found to be a sigmoidal function of width, with the MD probes achieving lower height compared to the metal-coated and the DC tips with comparable k Avg. This study expands the application of monolithic conductive polycrystalline diamond (PCD) probes with outstanding wear resistance to fine LAO lithography.

  8. Conductive polycrystalline diamond probes for local anodic oxidation lithography.

    PubMed

    Ulrich, A J; Radadia, A D

    2015-11-20

    This is the first report characterizing local anodic oxidation (LAO) lithography performed using conductive monolithic polycrystalline diamond (MD) and conductive polycrystalline diamond-coated (DC) tips and comparing it to the diamond-like carbon-coated and metal-coated silicon tips. The range and the rate of increase in the lithographic linewidth and height with tip bias (dw/dV and dh/dV) differed based on the tip material. The DC tips resulted in wider and taller lines and a higher dw/dV and dh/dV compared to metal-coated tips with a similar force constant (k(Avg)). The metal-coated and the DC tips with comparable k(Avg) showed comparable threshold voltages, whereas the MD tips with similar k(Avg) showed a higher threshold voltage. The MD tips exhibited less than half the height and nearly half the dw/dV and dh/dV obtained with the metal-coated tips with similar k Avg, thus also resulting in a smaller width at -10 V. The linewidths were found to be proportional to the inverse of the log of write speed(v) for all the tips; however, the proportionality constant varied with tip material; the DC tips had larger values, and the MD and the metal-coated tips had comparable values. When varying the speed, the height was found to be a sigmoidal function of width, with the MD probes achieving lower height compared to the metal-coated and the DC tips with comparable k(Avg). This study expands the application of monolithic conductive polycrystalline diamond (PCD) probes with outstanding wear resistance to fine LAO lithography. PMID:26501841

  9. Preparation of a porous Sn@C nanocomposite as a high-performance anode material for lithium-ion batteries

    NASA Astrophysics Data System (ADS)

    Zhang, Yanjun; Jiang, Li; Wang, Chunru

    2015-07-01

    A porous Sn@C nanocomposite was prepared via a facile hydrothermal method combined with a simple post-calcination process, using stannous octoate as the Sn source and glucose as the C source. The as-prepared Sn@C nanocomposite exhibited excellent electrochemical behavior with a high reversible capacity, long cycle life and good rate capability when used as an anode material for lithium ion batteries.A porous Sn@C nanocomposite was prepared via a facile hydrothermal method combined with a simple post-calcination process, using stannous octoate as the Sn source and glucose as the C source. The as-prepared Sn@C nanocomposite exhibited excellent electrochemical behavior with a high reversible capacity, long cycle life and good rate capability when used as an anode material for lithium ion batteries. Electronic supplementary information (ESI) available: Detailed experimental procedure and additional characterization, including a Raman spectrum, TGA curve, N2 adsorption-desorption isotherm, TEM images and SEM images. See DOI: 10.1039/c5nr03093e

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

    PubMed

    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

  11. Simulation, optimization and testing of a novel high spatial resolution X-ray imager based on Zinc Oxide nanowires in Anodic Aluminium Oxide membrane using Geant4

    NASA Astrophysics Data System (ADS)

    Esfandi, F.; Saramad, S.

    2015-07-01

    In this work, a new generation of scintillator based X-ray imagers based on ZnO nanowires in Anodized Aluminum Oxide (AAO) nanoporous template is characterized. The optical response of ordered ZnO nanowire arrays in porous AAO template under low energy X-ray illumination is simulated by the Geant4 Monte Carlo code and compared with experimental results. The results show that for 10 keV X-ray photons, by considering the light guiding properties of zinc oxide inside the AAO template and suitable selection of detector thickness and pore diameter, the spatial resolution less than one micrometer and the detector detection efficiency of 66% are accessible. This novel nano scintillator detector can have many advantages for medical applications in the future.

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

    NASA Astrophysics Data System (ADS)

    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.

  13. Porous metal oxide microspheres from ion exchange resin

    NASA Astrophysics Data System (ADS)

    Picart, S.; Parant, P.; Caisso, M.; Remy, E.; Mokhtari, H.; Jobelin, I.; Bayle, J. P.; Martin, C. L.; Blanchart, P.; Ayral, A.; Delahaye, T.

    2015-07-01

    This study is devoted to the synthesis and the characterization of porous metal oxide microsphere from metal loaded ion exchange resin. Their application concerns the fabrication of uranium-americium oxide pellets using the powder-free process called Calcined Resin Microsphere Pelletization (CRMP). Those mixed oxide ceramics are one of the materials envisaged for americium transmutation in sodium fast neutron reactors. The advantage of such microsphere precursor compared to classical oxide powder is the diminution of the risk of fine dissemination which can be critical for the handling of highly radioactive powders such as americium based oxides and the improvement of flowability for the filling of compaction chamber. Those millimetric oxide microspheres incorporating uranium and americium were synthesized and characterizations showed a very porous microstructure very brittle in nature which occurred to be adapted to shaping by compaction. Studies allowed to determine an optimal heat treatment with calcination temperature comprised between 700-800 °C and temperature rate lower than 2 °C/min. Oxide Precursors were die-pressed into pellets and then sintered under air to form regular ceramic pellets of 95% of theoretical density (TD) and of homogeneous microstructure. This study validated thus the scientific feasibility of the CRMP process to prepare bearing americium target in a powder free manner.

  14. A colorimetric sensor based on anodized aluminum oxide (AAO) substrate for the detection of nitroaromatics.

    SciTech Connect

    Liu, Y.; Wang, H. H.; Indacochea, J. E.; Wang, M. L.

    2011-12-15

    Simple and low cost colorimetric sensors for explosives detection were explored and developed. Anodized aluminum oxide (AAO) with large surface area through its porous structure and light background color was utilized as the substrate for colorimetric sensors. Fabricated thin AAO films with thickness less than {approx} 500 nm allowed us to observe interference colors which were used as the background color for colorimetric detection. AAO thin films with various thickness and pore-to-pore distance were prepared through anodizing aluminum foils at different voltages and times in dilute sulfuric acid. Various interference colors were observed on these samples due to their difference in structures. Accordingly, suitable anodization conditions that produce AAO samples with desired light background colors for optical applications were obtained. Thin film interference model was applied to analyze the UV-vis reflectance spectra and to estimate the thickness of the AAO membranes. We found that the thickness of produced AAO films increased linearly with anodization time in sulfuric acid. In addition, the growth rate was higher for AAO anodized using higher voltages. The thin film interference formulism was further validated with a well established layer by layer deposition technique. Coating poly(styrene sulfonate) sodium salt (PSS) and poly(allylamine hydrochloride) (PAH) layer by layer on AAO thin film consistently shifted its surface color toward red due to the increase in thickness. The red shift of UV-vis reflectance was correlated quantitatively to the number of layers been assembled. This sensitive red shift due to molecular attachment (increase in thickness) on AAO substrate was applied toward nitroaromatics detection. Aminopropyltrimethoxysilane (APTS) which can be attached onto AAO nanowells covalently through silanization and attract TNT molecules was coated and applied for TNT detection. UV-vis spectra of AAO with APTS shifted to the longer wavelength side due to

  15. Performance and durability of anode-supported flat-tubular solid oxide fuel cells with Ag-infiltrated cathodes.

    PubMed

    Pi, Seuk-Hoon; Lee, Jong-Won; Lee, Seung-Bok; Lim, Tak-Hyoung; Park, Seok-Joo; Park, Chong-Ook; Song, Rak-Hyun

    2014-10-01

    An anode-supported flat-tubular solid oxide fuel cell is an advanced cell design, which offers many advantages including a high volumetric power density, a minimized sealing area and a high resistance to thermal cycling. Infiltration of nano-sized noble metal catalysts into a porous cathode is known to be an effective method to improve cathode performances at reduced temperatures, but the cathode stability is of potential concern. This study addresses the performance and durability of anode-supported flat-tubular solid oxide fuel cells with Ag-infiltrated cathodes. Uniformly dispersed Ag nanoparticles on the cathode are formed via a wet infiltration technique combined with subsequent heat-treatment. Although the Ag infiltration results in improved cell performance, the durability tests indicate that the cell performance degrades over time and that the degradation rate increases with increasing Ag loading in the cathode. The observed performance degradation is mainly attributed to formation of large-scale Ag agglomerates. A strategy based on an inter-dispersed composite of Ag and CeO2 nanoparticles is proposed to mitigate the performance degradation. PMID:25942845

  16. Partial oxidation of dimethyl ether using the structured catalyst Rh/Al2O3/Al prepared through the anodic oxidation of aluminum.

    PubMed

    Yu, B Y; Lee, K H; Kim, K; Byun, D J; Ha, H P; Byun, J Y

    2011-07-01

    The partial oxidation of dimethyl ether (DME) was investigated using the structured catalyst Rh/Al2O3/Al. The porous Al2O3 layer was synthesized on the aluminum plate through anodic oxidation in an oxalic-acid solution. It was observed that about 20 nm nanopores were well developed in the Al2O3 layer. The thickness of Al2O3 layer can be adjusted by controlling the anodizing time and current density. After pore-widening and hot-water treatment, the Al2O3/Al plate was calcined at 500 degrees C for 3 h. The obtained delta-Al2O3 had a specific surface area of 160 m2/g, making it fit to be used as a catalyst support. A microchannel reactor was designed and fabricated to evaluate the catalytic activity of Rh/Al2O3/Al in the partial oxidation of DME. The structured catalyst showed an 86% maximum hydrogen yield at 450 degrees C. On the other hand, the maximum syngas yield by a pack-bed-type catalyst could be attained by using a more than fivefold Rh amount compared to that used in the structured Rh/Al2O3/Al catalyst. PMID:22121705

  17. Uranium Oxide Aerosol Transport in Porous Graphite

    SciTech Connect

    Blanchard, Jeremy; Gerlach, David C.; Scheele, Randall D.; Stewart, Mark L.; Reid, Bruce D.; Gauglitz, Phillip A.; Bagaasen, Larry M.; Brown, Charles C.; Iovin, Cristian; Delegard, Calvin H.; Zelenyuk, Alla; Buck, Edgar C.; Riley, Brian J.; Burns, Carolyn A.

    2012-01-23

    The objective of this paper is to investigate the transport of uranium oxide particles that may be present in carbon dioxide (CO2) gas coolant, into the graphite blocks of gas-cooled, graphite moderated reactors. The transport of uranium oxide in the coolant system, and subsequent deposition of this material in the graphite, of such reactors is of interest because it has the potential to influence the application of the Graphite Isotope Ratio Method (GIRM). The GIRM is a technology that has been developed to validate the declared operation of graphite moderated reactors. GIRM exploits isotopic ratio changes that occur in the impurity elements present in the graphite to infer cumulative exposure and hence the reactor’s lifetime cumulative plutonium production. Reference Gesh, et. al., for a more complete discussion on the GIRM technology.

  18. Inert anode containing oxides of nickel iron and cobalt useful for the electrolytic production of metals

    DOEpatents

    Ray, Siba P.; Liu, Xinghua; Weirauch, Jr., Douglas A.

    2002-01-01

    An inert anode for the electrolytic production of metals such as aluminum is disclosed. The inert anode includes a ceramic oxide material preferably made from NiO, Fe.sub.2 O.sub.3 and CoO. The inert anode composition may comprise the following mole fractions of NiO, Fe.sub.2 O.sub.3 and CoO: 0.15 to 0.99 NiO; 0.0001 to 0.85 Fe.sub.2 O.sub.3 ; and 0.0001 to 0.45 CoO. The inert anode may optionally include other oxides and/or at least one metal phase, such as Cu, Ag, Pd, Pt, Au, Rh, Ru, Ir and/or Os. The Ni--Fe--Co--O ceramic material exhibits very low solubility in Hall cell baths used to produce aluminum.

  19. Anode protection system for shutdown of solid oxide fuel cell system

    SciTech Connect

    Li, Bob X; Grieves, Malcolm J; Kelly, Sean M

    2014-12-30

    An Anode Protection Systems for a SOFC system, having a Reductant Supply and safety subsystem, a SOFC anode protection subsystem, and a Post Combustion and slip stream control subsystem. The Reductant Supply and safety subsystem includes means for generating a reducing gas or vapor to prevent re-oxidation of the Ni in the anode layer during the course of shut down of the SOFC stack. The underlying ammonia or hydrogen based material used to generate a reducing gas or vapor to prevent the re-oxidation of the Ni can be in either a solid or liquid stored inside a portable container. The SOFC anode protection subsystem provides an internal pressure of 0.2 to 10 kPa to prevent air from entering into the SOFC system. The Post Combustion and slip stream control subsystem provides a catalyst converter configured to treat any residual reducing gas in the slip stream gas exiting from SOFC stack.

  20. Nanopatterning of Crystalline Silicon Using Anodized Aluminum Oxide Templates for Photovoltaics

    NASA Astrophysics Data System (ADS)

    Chao, Tsu-An

    A novel thin film anodized aluminum oxide templating process was developed and applied to make nanopatterns on crystalline silicon to enhance the optical properties of silicon. The thin film anodized aluminum oxide was created to improve the conventional thick aluminum templating method with the aim for potential large scale fabrication. A unique two-step anodizing method was introduced to create high quality nanopatterns and it was demonstrated that this process is superior over the original one-step approach. Optical characterization of the nanopatterned silicon showed up to 10% reduction in reflection in the short wavelength range. Scanning electron microscopy was also used to analyze the nanopatterned surface structure and it was found that interpore spacing and pore density can be tuned by changing the anodizing potential.

  1. Inert anode containing oxides of nickel, iron and zinc useful for the electrolytic production of metals

    DOEpatents

    Ray, Siba P.; Weirauch, Jr., Douglas A.; Liu, Xinghua

    2002-01-01

    An inert anode for the electrolytic production of metals such as aluminum is disclosed. The inert anode includes a ceramic oxide material preferably made from NiO, Fe.sub.2 O.sub.3 and ZnO. The inert anode composition may comprise the following mole fractions of NiO, Fe.sub.2 O.sub.3 and ZnO: 0.2 to 0.99 NiO; 0.0001 to 0.8 Fe.sub.2 O.sub.3 ; and 0.0001 to 0.3 ZnO. The inert anode may optionally include other oxides and/or at least one metal phase, such as Cu, Ag, Pd, Pt, Au, Rh, Ru, Ir and/or Os. The Ni--Fe--Co--O ceramic material exhibits very low solubility in Hall cell baths used to produce aluminum.

  2. Dimensions of luminescent oxidized and porous silicon structures

    SciTech Connect

    Schuppler, S.; Friedman, S.L.; Marcus, M.A.; Adler, D.L.; Xie, Y.; Ross, F.M.; Harris, T.D.; Brown, W.L.; Chabal, Y.J.; Brus, L.E.; Citrin, P.H. National Center for Electron Microscopy, Lawrence Berkeley Laboratory, Berkeley, California 94720 )

    1994-04-18

    X-ray absorption measurements from H-passivated porous Si and from oxidized Si nanocrystals, combined with electron microscopy, ir absorption, [alpha] recoil, and luminescence emission data, provide a consistent structural picture of the species responsible for the visible luminescence observed in these samples. The mass-weighted average structures in por-Si are particles, not wires, with dimensions significantly smaller than previously reported or proposed.

  3. Temperature evolution of copper oxide nanoparticles in porous glasses

    SciTech Connect

    Golosovsky, I. V.; Naberezhnov, A. A.; Kurdyukov, D. A.; Mirebeau, I.; Andre, G.

    2011-01-15

    The temperature evolution of copper oxide nanoparticles in the temperature range of 1.5-250 K has been investigated by thermal-neutron diffraction. CuO particles were obtained by Cu(NO{sub 3}){sub 2} {center_dot} 3H{sub 2}O decomposition directly in the pores of porous glass with an average pore diameter of 7 nm. The characteristic nanoparticle size and linear thermal expansion coefficients have been determined.

  4. Study of Sodium Ion Selective Electrodes and Differential Structures with Anodized Indium Tin Oxide

    PubMed Central

    Lin, Jyh-Ling; Hsu, Hsiang-Yi

    2010-01-01

    The objective of this work is the study and characterization of anodized indium tin oxide (anodized-ITO) as a sodium ion selective electrode and differential structures including a sodium-selective-membrane/anodized-ITO as sensor 1, an anodized-ITO membrane as the contrast sensor 2, and an ITO as the reference electrode. Anodized-ITO was fabricated by anodic oxidation at room temperature, a low cost and simple manufacture process that makes it easy to control the variation in film resistance. The anodized-ITO based on EGFET structure has good linear pH sensitivity, approximately 54.44 mV/pH from pH 2 to pH 12. The proposed sodium electrodes prepared by PVC-COOH, DOS embedding colloid, and complex Na-TFBD and ionophore B12C4, show good sensitivity at 52.48 mV/decade for 10−4 M to 1 M, and 29.96 mV/decade for 10−7 M to 10−4 M. The sodium sensitivity of the differential sodium-sensing device is 58.65 mV/decade between 10−4 M and 1 M, with a corresponding linearity of 0.998; and 19.17 mV/decade between 10−5 M and 10−4 M. PMID:22294900

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

    NASA Astrophysics Data System (ADS)

    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.

  6. Porous platinum mesoflowers with enhanced activity for methanol oxidation reaction

    SciTech Connect

    Zhuang Lina; Wang Wenjin; Hong Feng; Yang Shengchun; You Hongjun; Fang Jixiang; Ding Bingjun

    2012-07-15

    Porous Pt and Pt-Ag alloy mesoflowers (MFs) with about 2 {mu}m in diameter and high porosity were synthesized using Ag mesoflowers as sacrificial template by galvanic reaction. The silver content in Pt-Ag alloys can be facilely controlled by nitric acid treatment. And the pure Pt MFs can be obtained by selective removal of silver element from Pt{sub 72}Ag{sub 28} MFs electrochemically. Both Pt{sub 45}Ag{sub 55}, Pt{sub 72}Ag{sub 28} and pure Pt show a high catalytic performance in methanol oxidation reaction (MOR). Especially, pure Pt MFs exhibited a 2 to 3 times current density enhancement in MOR compared with the commercial used Pt black, which can be attributed to their porous nanostructure with 3-dimentional nature and small crystal sizes. - Graphical Abstract: The CVs of MOR on Pt (red) and Pt black (green) catalysts in 0.1 M HClO{sub 4} and 0.5 M CH{sub 3}OH for specific mass current. The insert shows the SEM images of two porous Pt MFs. Platinum mesoflowers (MFs) with about 2 {mu}m in diameter and high porosity were synthesised with Ag mesoflowers as sacrificial template by galvanic replacement. The porous Pt MFs exhibited a more than 3 times enhancement in electrocatalytic performance for methanol oxidation reaction compared the commercial used Pt black. Highlights: Black-Right-Pointing-Pointer Porous Pt and Pt-Ag mesoflowers (MFs) were synthesized using Ag MFs sacrifical template. Black-Right-Pointing-Pointer Pt MFs presents an improved catalytic activity in MOR compared with Pt black. Black-Right-Pointing-Pointer We provided a facile approach for the development of high performance Pt electrocatalysts for fuel cells.

  7. Novel Sulfur-Tolerant Anodes for Solid Oxide Fuel Cells

    SciTech Connect

    Lei Yang; Meilin Liu

    2008-12-31

    One of the unique advantages of SOFCs over other types of fuel cells is the potential for direct utilization of hydrocarbon fuels (it may involve internal reforming). Unfortunately, most hydrocarbon fuels contain sulfur, which would dramatically degrade SOFC performance at parts-per-million (ppm) levels. Low concentration of sulfur (ppm or below) is difficult to remove efficiently and cost-effectively. Therefore, knowing the exact poisoning process for state-of-the-art anode-supported SOFCs with Ni-YSZ cermet anodes, understanding the detailed anode poisoning mechanism, and developing new sulfur-tolerant anodes are essential to the promotion of SOFCs that run on hydrocarbon fuels. The effect of cell operating conditions (including temperature, H{sub 2}S concentration, cell voltage/current density, etc.) on sulfur poisoning and recovery of nickel-based anode in SOFCs was investigated. It was found that sulfur poisoning is more severe at lower temperature, higher H{sub 2}S concentration or lower cell current density (higher cell voltage). In-situ Raman spectroscopy identified the nickel sulfide formation process on the surface of a Ni-YSZ electrode and the corresponding morphology change as the sample was cooled in H{sub 2}S-containing fuel. Quantum chemical calculations predicted a new S-Ni phase diagram with a region of sulfur adsorption on Ni surfaces, corresponding to sulfur poisoning of Ni-YSZ anodes under typical SOFC operating conditions. Further, quantum chemical calculations were used to predict the adsorption energy and bond length for sulfur and hydrogen atoms on various metal surfaces. Surface modification of Ni-YSZ anode by thin Nb{sub 2}O{sub 5} coating was utilized to enhance the sulfur tolerance. A multi-cell testing system was designed and constructed which is capable of simultaneously performing electrochemical tests of 12 button cells in fuels with four different concentrations of H{sub 2}S. Through systematical study of state-of-the-art anode

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

    PubMed

    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

  9. Novel synthesis of holey reduced graphene oxide (HRGO) by microwave irradiation method for anode in lithium-ion batteries.

    PubMed

    Alsharaeh, Edreese; Ahmed, Faheem; Aldawsari, Yazeed; Khasawneh, Majdi; Abuhimd, Hatem; Alshahrani, Mohammad

    2016-01-01

    In this work, holey reduced graphene oxide (HRGO) was synthesized by the deposition of silver (Ag) nanoparticles onto the reduced graphene oxide (RGO) sheets followed by nitric acid treatment to remove Ag nanoparticles by microwave irradiation to form a porous structure. The HRGO were characterized by X-ray diffraction (XRD), field-emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), ultra violet-visible spectroscopy (UV-Vis), thermogravimetric analysis (TGA), and Raman spectroscopy. These novel HRGO exhibited high rate capability with excellent cycling stability as an anode material for lithium-ion batteries. The results have shown an excellent electrochemical response in terms of charge/discharge capacity (423 mAh/g at 100 mA/g). The cyclic performance was also exceptional as a high reversible capacity (400 mAh/g at 100 mA/g) was retained for 100 charge/discharge cycles. This fascinating electrochemical performance can be ascribed to their specific porous structure (2-5 nm pores) and high surface area (457 m(2)/g), providing numerous active sites for Li(+) insertion, high electrical conductivity, low charge-transfer resistance across the electrolyte-electrode interface, and improved structural stability against the local volume change during Li(+) insertion-extraction. Such electrodes are envisioned to be mass scalable with relatively simple and low-cost fabrication procedures, thereby providing a clear pathway toward commercialization. PMID:27457356

  10. Novel synthesis of holey reduced graphene oxide (HRGO) by microwave irradiation method for anode in lithium-ion batteries

    NASA Astrophysics Data System (ADS)

    Alsharaeh, Edreese; Ahmed, Faheem; Aldawsari, Yazeed; Khasawneh, Majdi; Abuhimd, Hatem; Alshahrani, Mohammad

    2016-07-01

    In this work, holey reduced graphene oxide (HRGO) was synthesized by the deposition of silver (Ag) nanoparticles onto the reduced graphene oxide (RGO) sheets followed by nitric acid treatment to remove Ag nanoparticles by microwave irradiation to form a porous structure. The HRGO were characterized by X-ray diffraction (XRD), field-emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), ultra violet-visible spectroscopy (UV-Vis), thermogravimetric analysis (TGA), and Raman spectroscopy. These novel HRGO exhibited high rate capability with excellent cycling stability as an anode material for lithium-ion batteries. The results have shown an excellent electrochemical response in terms of charge/discharge capacity (423 mAh/g at 100 mA/g). The cyclic performance was also exceptional as a high reversible capacity (400 mAh/g at 100 mA/g) was retained for 100 charge/discharge cycles. This fascinating electrochemical performance can be ascribed to their specific porous structure (2–5 nm pores) and high surface area (457 m2/g), providing numerous active sites for Li+ insertion, high electrical conductivity, low charge-transfer resistance across the electrolyte–electrode interface, and improved structural stability against the local volume change during Li+ insertion–extraction. Such electrodes are envisioned to be mass scalable with relatively simple and low-cost fabrication procedures, thereby providing a clear pathway toward commercialization.

  11. Novel synthesis of holey reduced graphene oxide (HRGO) by microwave irradiation method for anode in lithium-ion batteries

    PubMed Central

    Alsharaeh, Edreese; Ahmed, Faheem; Aldawsari, Yazeed; Khasawneh, Majdi; Abuhimd, Hatem; Alshahrani, Mohammad

    2016-01-01

    In this work, holey reduced graphene oxide (HRGO) was synthesized by the deposition of silver (Ag) nanoparticles onto the reduced graphene oxide (RGO) sheets followed by nitric acid treatment to remove Ag nanoparticles by microwave irradiation to form a porous structure. The HRGO were characterized by X-ray diffraction (XRD), field-emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), ultra violet-visible spectroscopy (UV-Vis), thermogravimetric analysis (TGA), and Raman spectroscopy. These novel HRGO exhibited high rate capability with excellent cycling stability as an anode material for lithium-ion batteries. The results have shown an excellent electrochemical response in terms of charge/discharge capacity (423 mAh/g at 100 mA/g). The cyclic performance was also exceptional as a high reversible capacity (400 mAh/g at 100 mA/g) was retained for 100 charge/discharge cycles. This fascinating electrochemical performance can be ascribed to their specific porous structure (2–5 nm pores) and high surface area (457 m2/g), providing numerous active sites for Li+ insertion, high electrical conductivity, low charge-transfer resistance across the electrolyte–electrode interface, and improved structural stability against the local volume change during Li+ insertion–extraction. Such electrodes are envisioned to be mass scalable with relatively simple and low-cost fabrication procedures, thereby providing a clear pathway toward commercialization. PMID:27457356

  12. Magnesiothermically reduced diatomaceous earth as a porous silicon anode material for lithium ion batteries

    NASA Astrophysics Data System (ADS)

    Shen, Lanyao; Guo, Xianwei; Fang, Xiangpeng; Wang, Zhaoxiang; Chen, Liquan

    2012-09-01

    Three-dimensional porous silicon has been prepared by magnesiothermically reducing diatomaceous earth. BET surface area analysis shows that the specific surface area of the obtained porous silicon is about 96 m2 g-1, much higher than that of the diatomaceous earth (6 m2 g-1). The silicon products after HCl immersion have a porous structure similar to that of the diatomaceous earth, with pore sizes around 200 nm. Galvanostatic cycling tests show that the initial charge and discharge capacities of the porous silicon are 1321 mAh g-1 and 1818 mAh g-1, respectively. A reversible capacity of 633 mAh g-1 is retained after 30 cycles.

  13. Detailed impedance characterization of a well performing and durable Ni:CGO infiltrated cermet anode for metal-supported solid oxide fuel cells

    NASA Astrophysics Data System (ADS)

    Nielsen, Jimmi; Klemensø, Trine; Blennow, Peter

    2012-12-01

    Further knowledge of the novel, well performing and durable Ni:CGO infiltrated cermet anode for metal supported fuel cells has been acquired by means of a detailed impedance spectroscopy study. The anode impedance was shown to consist of three arcs. Porous electrode theory (PET) represented as a transmission line response could account for the intermediate frequency arc. The PET model enabled a detailed insight into the effect of adding minor amounts of Ni into the infiltrated CGO and allowed an estimation of important characteristics such as the electrochemical utilization thickness of the anode. Furthermore, the study also revealed that the observed high frequency impedance arc cannot solely be a consequence of the grain boundaries within the electrolyte as previous studies have assumed. Instead, the results pointed towards an oxide ion charge transfer resistance between the electrolyte and the infiltrated anode. The low frequency impedance arc was in accordance with previous studies interpreted to be associated with the gas concentration. Finally, the robustness of the infiltration towards sintering and/or agglomeration at elevated temperature was studied. The results showed that the performance of the infiltrated submicron sized particles was surprisingly robust. TEM analysis revealed the nano sized Ni particles to be trapped within the CGO matrix, which along the self limiting grain growth of the CGO seem to be able to stabilize the submicron structured anode.

  14. LOW-TEMPERATURE, ANODE-SUPPORTED HIGH POWER DENSITY SOLID OXIDE FUEL CELLS WITH NANOSTRUCTURED ELECTRODES

    SciTech Connect

    Anil V. Virkar

    2001-06-21

    A simple, approximate analysis of the effect of differing cathode and anode areas on the measurement of cell performance on anode-supported solid oxide fuel cells, wherein the cathode area is smaller than the anode area, is presented. It is shown that the effect of cathode area on cathode polarization, on electrolyte contribution, and on anode resistance, as normalized on the basis of the cathode area, is negligible. There is a small but measurable effect on anode polarization, which results from concentration polarization. Effectively, it is the result of a greater amount of fuel transported to the anode/electrolyte interface in cases wherein the anode area is larger than the cathode area. Experiments were performed on cells made with differing cathode areas and geometries. Cathodic and anodic overpotentials measured using reference electrodes, and the measured ohmic area specific resistances by current interruption, were in good agreement with expectations based on the analysis presented. At 800 C, the maximum power density measured with a cathode area of {approx}1.1 cm{sup 2} was {approx}1.65 W/cm{sup 2} compared to {approx}1.45 W/cm{sup 2} for cathode area of {approx}2 cm{sup 2}, for anode thickness of {approx}1.3 mm, with hydrogen as the fuel and air as the oxidant. At 750 C, the measured maximum power densities were {approx}1.3 W/cm{sup 2} for the cell with cathode area {approx}1.1 cm{sup 2}, and {approx}1.25 W/cm{sup 2} for the cell with cathode area {approx}2 cm{sup 2}.

  15. Porous reduced graphene oxide membrane with enhanced gauge factor

    NASA Astrophysics Data System (ADS)

    Li, Jen-Chieh; Weng, Cheng-Hsi; Tsai, Fu-Cheng; Shih, Wen-Pin; Chang, Pei-Zen

    2016-01-01

    This paper shows that a porous structure for a reduced graphene oxide (rGO) membrane effectively enhances its gauge factor. A porous graphene-based membrane was synthesized in a liquid phase by combining a GO sheet with copper hydroxide nanostrands (CHNs). A chemical reduction treatment using L-ascorbic acid was utilized to simultaneously improve the conductivity of GO and remove the CHNs from each GO sheet. The intrinsic gauge factors of the porous rGO membrane with varying applied tensile strains were obtained and found to increase monotonically with the increased porosity of the rGO membrane. For a membrane porosity of 15.78%, the maximum gauge factor is 46.1 under an applied strain of less than 1%. The main mechanism behind the enhanced gauge factor is attributed to the structure of the porous rGO membrane. The relationships between the initial electrical resistance, tunneling distance, and gauge factor of the rGO membrane were found by adjusting the membrane porosity and the results completely confirmed the physical phenomena.

  16. Hierarchical porous anatase TiO2 derived from a titanium metal-organic framework as a superior anode material for lithium ion batteries.

    PubMed

    Xiu, Zhiliang; Alfaruqi, Muhammad Hilmy; Gim, Jihyeon; Song, Jinju; Kim, Sungjin; Vu Thi, Trang; Duong, Pham Tung; Baboo, Joseph Paul; Mathew, Vinod; Kim, Jaekook

    2015-08-01

    Hierarchical meso-/macroporous anatase TiO2 was synthesized by the hydrolysis of a titanium metal-organic framework precursor followed by calcination in air. This unique porous feature enables the superior rate capability and excellent cycling stability of anatase TiO2 as an anode for rechargeable lithium-ion batteries. PMID:26137998

  17. A hierarchical Zn2Mo3O8 nanodots-porous carbon composite as a superior anode for lithium-ion batteries.

    PubMed

    Zhu, Yanping; Zhong, Yijun; Chen, Gao; Deng, Xiang; Cai, Rui; Li, Li; Shao, Zongping

    2016-08-01

    A hierarchical Zn2Mo3O8 nanodots-porous carbon composite has been successfully synthesized via the ingenious combination of ion exchange and molten salt strategies, and the composite exhibits remarkable performance as an anode material for lithium-ion batteries. PMID:27374699

  18. Porous carbon particles derived from natural peanut shells as lithium ion battery anode and its electrochemical properties

    NASA Astrophysics Data System (ADS)

    Cao, Xiaoyu; Chen, Shuangqiang; Wang, Guoxiu

    2014-07-01

    Abandoned peanut shells, a common farm waste, have caused tremendous environmental pollution and huge waste deposits through burned and buried disposal approaches. In targeting to enhance the potential value of peanut shells and discover a new alternative candidate for lithium ion batteries, we adopted an easy to scale-up and highly repeated method to treat fresh and dry peanut shells via acid-treatment and pyrolysis, making porous structures on carbonized peanut shells. The pyrolysis process transformed the peanut shells to porous carbon (PC) materials in a quartz tube furnace at a series of temperatures from 500°C to 700°C in N2 under the condition of 40°C gradient temperatures with a heating rate of 2°C min-1. Scanning electron microscopy (SEM) images show that the irregular porous structures and hundreds of micropores are distributed on the PC materials. The cyclic voltammogram (CV) test and particle size analysis are employed to investigate their characteristics of voltammetry and particle size distribution. PC material obtained at 620°C (PC-620) exhibited good particle distribution, porous structure and less agglomerated particles. When applied as anode materials in lithium ion batteries, the PC-620 electrode displayed the high reversible capacity of 608 mAh g-1. Moreover, the cycling performance of PC-620 was the most stable, with a high Coulombic efficiency of 98.9% at the 20th cycle, demonstrating a reversible capacity of 418 mAh g-1, which is higher than the theoretical capacity of graphite. Most importantly, the PC materials harvested from the wastes of natural resources are turned into valuable electrode materials for the high demand energy storage devices, which can significantly reduce severe environmental pollution and alleviate an energy shortage. [Figure not available: see fulltext.

  19. Determination of sulfuric acid concentration for anti-cavitation characteristics of Al alloy by two step anodizing process to forming nano porous.

    PubMed

    Lee, Seung-Jun; Kim, Seong-Kweon; Jeong, Jae-Yong; Kim, Seong-Jong

    2014-12-01

    Al alloy is a highly active metal but forms a protective oxide film having high corrosion resistance in atmosphere environment. However, the oxide film is not suitable for practical use, since the thickness of the film is not uniform and it is severly altered with formation conditions. This study focused on developing an aluminum anodizing layer having hardness, corrosion resistance and abrasion resistance equivalent to a commercial grade protective layer. Aluminum anodizing layer was produced by two-step aluminum anodizing oxide (AAO) process with different sulfuric acid concentrations, and the cavitation characteristics of the anodized coating layer was investigated. In hardness measurement, the anodized coating layer produced with 15 vol.% of sulfuric acid condition had the highest value of hardness but exhibited poor cavitation resistance due to being more brittle than those with other conditions. The 10 vol.% of sulfuric acid condition was thus considered to be the optimum condition as it had the lowest weight loss and damage depth. PMID:25971100

  20. Acidity and aluminum toxicity caused by iron oxidation around anode bars

    SciTech Connect

    Shen, S.; Pepper, G.E.; Hassett, J.J.; Stucki, J.W.

    1998-08-01

    Soil acidity and aluminum toxicity are serious environmental problems often found in humid temperate and tropical regions or in areas with acid rain. Iron oxidation in soils can also cause high concentrations of H{sup +}, which, in turn, causes an increase of Al{sup 3+} in the soil solution. To examine this problem, a study was undertaken to discover the cause of crop damage in crops planted over buried anode bars. Anode bars are part of an impressed current cathodic protection system for pipelines near Decatur, Illinois. Soil samples were collected from the problem site and from a non-problem site for comparison. Results showed that Fe oxidation around anode bars at the problem site is stimulated by electric current, a situation that results in high concentrations of H{sup +} and reduces soil pH to less than 3.0. Under the low pH condition, the content of available Al is very high, and therefore, the soil solution becomes toxic for soybean roots. Exchangeable Al was 360 to 700 ppm in soil immediately adjacent to anode bars but only 3 ppm in the soil midway between anode bars. The damage to the plants, such as reduced vegetative growth and lowered seed yield, developed in a circular pattern over the anode bars. Factors contributing to the problem were soil Fe content, rectifier voltage, and soil drainage.

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

    PubMed

    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

  2. For cermet inert anode containing oxide and metal phases useful for the electrolytic production of metals

    DOEpatents

    Ray, Siba P.; Liu, Xinghua; Weirauch, Douglas A.

    2002-01-01

    A cermet inert anode for the electrolytic production of metals such as aluminum is disclosed. The inert anode comprises a ceramic phase including an oxide of Ni, Fe and M, where M is at least one metal selected from Zn, Co, Al, Li, Cu, Ti, V, Cr, Zr, Nb, Ta, W, Mo, Hf and rare earths, preferably Zn and/or Co. Preferred ceramic compositions comprise Fe.sub.2 O.sub.3, NiO and ZnO or CoO. The cermet inert anode also comprises a metal phase such as Cu, Ag, Pd, Pt, Au, Rh, Ru, Ir and/or Os. A preferred metal phase comprises Cu and Ag. The cermet inert anodes may be used in electrolytic reduction cells for the production of commercial purity aluminum as well as other metals.

  3. Pilot demonstration of cerium oxide coated anodes. Final report, April 1990--October 1992

    SciTech Connect

    Gregg, J.S.; Frederick, M.S.; Shingler, M.J.; Alcorn, T.R.

    1992-10-01

    Cu cermet anodes were tested for 213 to 614 hours with an in-situ deposited CEROX coating in a pilot cell operated by Reynolds Manufacturing Technology Laboratory. At high bath ratio ({approximately}1.5) and low current density (0.5 A/cm{sup 2}), a {ge}1 mm thick dense CEROX coating was deposited on the anodes. At lower bath ratios and higher current density, the CEROX coating was thinner and less dense, but no change in corrosion rate was noted. Regions of low current density on the anodes and sides adjacent to the carbon anode sometimes had thin or absent CEROX coatings. Problems with cracking and oxidation of the cermet substrates led to higher corrosion rates in a pilot cell than would be anticipated from lab scale results.

  4. Tailoring morphology in free-standing anodic aluminium oxide: control of barrier layer opening down to the sub-10 nm diameter.

    PubMed

    Gong, Jie; Butler, William H; Zangari, Giovanni

    2010-05-01

    Free-standing, highly ordered porous aluminium oxide templates were fabricated by three-step anodization in oxalic, sulfuric or phosphoric acid solutions, followed by dissolution of the aluminium substrate in HgCl(2). Opening of the pore bottoms on the barrier layer side of these templates was carried out by using chemical or ion beam etching. Chemical etching is capable of achieving full pore opening, but partial pore opening occurs inhomogeneously. On the contrary, ion beam etching enables homogeneous and reproducible partial pore opening, with the pore size controlled through the etching time. By this method, pore openings as small as 5 nm can reliably be obtained. PMID:20648324

  5. Effect of Anodic Alumina Oxide Pore Diameter on the Crystallization of Poly(butylene adipate).

    PubMed

    Sun, Xiaoli; Fang, Qunqun; Li, Huihui; Ren, Zhongjie; Yan, Shouke

    2016-04-01

    Poly(butylene adipate) (PBA) was infiltrated into the anodic alumina oxide (AAO) templates with the pore diameter of around 30, 70, and 100 nm and PBA nanotubes with different diameters were prepared. The crystallization and phase transition behavior of the obtained PBA nanotubes capped in the nanopores have been explored by using X-ray diffraction and differential scanning calorimetry. Only α-PBA crystals form in the bulk sample during nonisothermal crystallization. By contrast, predominant β-PBA crystals form in the AAO templates. The β-PBA crystals formed in the nanopores with pore diameter less than 70 nm prefer to adopt an orientation with their b-axis parallel to the long axis of the pore. During the melt recrystallization, it was found that the critical temperature (Tβ), below which pure β-crystals form, is 20 °C for bulk PBA. It drops down significantly with the pore diameter for the PBA in the AAO template. Moreover, the β-crystals in the porous template exhibit larger lattice parameters compared with the bulk crystals. By monitoring the change of β-crystals in the heating process, it was found that β-crystals in the AAO template with the pore diameter of 30 nm (D30) melt directly while the β-crystals transform to α-crystals in the template with the pore diameter of 100 nm (D100). The intensity of (020) Bragg peak of β-crystals decreases at a similar rate in both D30 and D100 but disappears at a relatively lower temperature in D30. On the other hand, the β(110) peak intensity of β-PBA crystals formed in the D100 template decreases first at slower rate before α crystals appear, and then at a faster rate once the β to α phase transition takes place. PMID:27008378

  6. Effect of Natural Gas Fuel Addition on the Oxidation of Fuel Cell Anode Gas

    SciTech Connect

    Randall S. Gemmen; Edward H. Robey, Jr.

    1999-11-01

    The anode exhaust gas from a fuel cell commonly has a fuel energy density between 15 and 25% that of the fuel supply, due to the incomplete oxidation of the input fuel. This exhaust gas is subsequently oxidized (catalytically or non-catalytically), and the resultant thermal energy is often used elsewhere in the fuel cell process. Alternatively, additional fuel can be added to this stream to enhance the oxidation of the stream, for improved thermal control of the power plant, or to adjust the temperature of the exhaust gas as may be required in other specialty co-generation applications. Regardless of the application, the cost of a fuel cell system can be reduced if the exhaust gas oxidation can be accomplished through direct gas phase oxidation, rather than the usual catalytic oxidation approach. Before gas phase oxidation can be relied upon however, combustor design requirements need to be understood. The work reported here examines the issue of fuel addition, primarily as related to molten-carbonate fuel cell technology. It is shown experimentally that without proper combustor design, the addition of natural gas can readily quench the anode gas oxidation. The Chemkin software routines were used to resolve the mechanisms controlling the chemical quenching. It is found that addition of natural gas to the anode exhaust increases the amount of CH3 radicals, which reduces the concentration of H and O radicals and results in decreased rates of overall fuel oxidation.

  7. Hierarchical porous nitrogen-doped carbon nanosheets derived from silk for ultrahigh-capacity battery anodes and supercapacitors.

    PubMed

    Hou, Jianhua; Cao, Chuanbao; Idrees, Faryal; Ma, Xilan

    2015-03-24

    Hierarchical porous nitrogen-doped carbon (HPNC) nanosheets (NS) have been prepared via simultaneous activation and graphitization of biomass-derived natural silk. The as-obtained HPNC-NS show favorable features for electrochemical energy storage such as high specific surface area (SBET: 2494 m(2)/g), high volume of hierarchical pores (2.28 cm(3)/g), nanosheet structures, rich N-doping (4.7%), and defects. With respect to the multiple synergistic effects of these features, a lithium-ion battery anode and a two-electrode-based supercapacitor have been prepared. A reversible lithium storage capacity of 1865 mA h/g has been reported, which is the highest for N-doped carbon anode materials to the best of our knowledge. The HPNC-NS supercapacitor's electrode in ionic liquid electrolytes exhibit a capacitance of 242 F/g and energy density of 102 W h/kg (48 W h/L), with high cycling life stability (9% loss after 10,000 cycles). Thus, a high-performance Li-ion battery and supercapacitors were successfully assembled for the same electrode material, which was obtained through a one-step and facile large-scale synthesis route. It is promising for next-generation hybrid energy storage and renewable delivery devices. PMID:25703427

  8. Self-assembled porous MoO2/graphene microspheres towards high performance anodes for lithium ion batteries

    NASA Astrophysics Data System (ADS)

    Palanisamy, Kowsalya; Kim, Yunok; Kim, Hansu; Kim, Ji Man; Yoon, Won-Sub

    2015-02-01

    Three dimensional (3D) porous self-assembled MoO2/graphene microspheres are successfully synthesized via microwave-assisted hydrothermal process in a short reaction time followed by thermal annealing. Such rationally designed multifunctional hybrid nanostructure is constructed from interconnected MoO2 nanoparticles (3-5 nm), which is self-assembled into ordered nanoporous microspheres via strong electrostatic attraction between graphene sheets and MoO2 nanoparticles. The MoO2/graphene hybrid structure delivers a high reversible capacity with significantly enhanced cycling stability (∼1300 mAh g-1 after 80 cycles at C/10 rate) and excellent rate capability (913 and 390 mAh g-1 at 2C and 5C rates, respectively), when used as an anode material. The microspheres are interconnected and well encapsulated by the flexible graphene sheets, which not only accommodates large volume change but also increases the electrical conductivity of the hybrid structure. Moreover, nanoporous voids present in the 3D framework facilitate effective electrolyte penetration and make a direct contact with the active MoO2 nanoparticles, thereby greatly enhancing lithium ion transport. The strategic combination of self-assembly, nanoporous voids, 3D network and intriguing properties of graphene sheets provides excellent electrochemical performance as anode materials for Lithium ion battery applications.

  9. Label-Free Detection of Telomerase Activity in Urine Using Telomerase-Responsive Porous Anodic Alumina Nanochannels.

    PubMed

    Liu, Xu; Wei, Min; Liu, Yuanjian; Lv, Bingjing; Wei, Wei; Zhang, Yuanjian; Liu, Songqin

    2016-08-16

    Telomerase is closely related to cancers, which makes it one of the most widely known tumor marker. Recently, many methods have been reported for telomerase activity measurement in which complex label procedures were commonly used. In this paper, a label-free method for detection of telomerase activity in urine based on steric hindrance changes induced by confinement geometry in the porous anodic alumina (PAA) nanochannels was proposed. Telomerase substrate (TS) primer was first assembled on the inside wall of PAA nanochannels by Schiff reaction under mild conditions. Then, under the action of telomerase, TS primer was amplified and extended to repeating G-rich sequences (TTAGGG)x, which formed multiplex G-quadruplex in the presence of potassium ions (K(+)). This configurational change led to the increment of steric hindrance in the nanochannels, resulting in the decrement of anodic current of potassium ferricyanide (K3[Fe(CN)6]). Compared with previously reported methods based on PAA nanochannels (usually one G-quadruplex formed), multiplex repeating G-quadruplex formed on one TS primer in this work. As a result, large current drop (∼3.6 μA, 36%) was obtained, which gave facility to improve the detection sensitivity. The decreased ratio of anodic current has a linear correlation with the logarithm of HeLa cell number in the range of 10-5000 cells, with the detection limit of seven cells. The method is simple, reliable, and has been successfully applied in the detection of telomerase in urine with good accuracy, selectivity and reproducibility. In addition, the method is nondestructive test compared to blood analysis and pathology tests, which is significant for cancer discovery, development, and prognosis. PMID:27420905

  10. Fabrication of a Ni nano-imprint stamp for an anti-reflective layer using an anodic aluminum oxide template.

    PubMed

    Park, Eun-Mi; Lim, Seung-Kyu; Ra, Senug-Hyun; Suh, Su-Jung

    2013-11-01

    Aluminum anodizing can alter pore diameter, density distribution, periodicity and layer thickness in a controlled way. Because of this property, porous type anodic aluminum oxide (AAO) was used as a template for nano-structure fabrication. The alumina layer generated at a constant voltage increased the pore size from 120 nm to 205 nm according to an increasing process time from 60 min to 150 min. The resulting fabricated AAO templates had pore diameters at or less than 200 nm. Ni was sputtered as a conductive layer onto this AAO template and electroplated using DC and pulse power. Comparing these Ni stamps, those generated from electroplating using on/reverse/off pulsing had an ordered pillar array and maintained the AAO template morphology. This stamp was used for nano-imprinting on UV curable resin coated glass wafer. Surface observations via electron microscopy showed that the nano-imprinted patterned had the same shape as the AAO template. A soft mold was subsequently fabricated and nano-imprinted to form a moth-eye structure on the glass wafer. An analysis of the substrate transmittance using UV-VIS/NIR spectroscopy showed that the transmittance of the substrate with the moth-eye structure was 5% greater that the non-patterned substrate. PMID:24245297

  11. Characterization of thin hydroxyapatite layers formed on anodic titanium oxide films containing Ca and P by hydrothermal treatment.

    PubMed

    Ishizawa, H; Ogino, M

    1995-09-01

    An anodic titanium oxide film containing Ca and P (AOFCP) was formed on commercially pure titanium which was anodized in an electrolytic solution of dissolved beta-glycerophosphate (beta-GP) and calcium acetate (CA). Hydroxyapatite (HA) crystals were precipitated by hydrothermally heating the AOFCP at 300 degrees C. After hydrothermal treatment, the film was characterized by scanning electron microscopy (SEM), energy-dispersive X-ray microanalysis (EDX), and tensile tests. The morphology, composition, and amount of HA crystals precipitated were significantly affected by the composition of the electrolytes. Near-stoichiometric HA crystals with high crystallinity were precipitated completely covering the AOFCP surface at specific electrolyte concentrations. The HA layers were thin at 1-2 microns in thickness. The adhesive strength of the film increased with decreasing electrolyte concentration and the maximum value was about 40 MPa. In vitro tests for 300 days suggested that the stability of the film was high. The high adhesive strength may result from the AOFCP existing as an intermediate layer between the HA layer and a titanium substrate. The intervention of the AOFCP may have prevented abrupt changes in Ca and P content at an HA coating-titanium interface as seen in a plasma-sprayed one. The porous TiO2 matrix of the AOFCP may be suitable for nucleation sites of HA crystals, as well as SiO2 matrix of silicate bioactive glasses or glass ceramics. PMID:8567705

  12. Preparation and analysis of anodic aluminum oxide films with continuously tunable interpore distances

    NASA Astrophysics Data System (ADS)

    Qin, Xiufang; Zhang, Jinqiong; Meng, Xiaojuan; Deng, Chenhua; Zhang, Lifang; Ding, Guqiao; Zeng, Hao; Xu, Xiaohong

    2015-02-01

    Nanoporous anodic aluminum oxides are often used as templates for preparation of nanostructures such as nanodot, nanowire and nanotube arrays. The interpore distance of anodic aluminum oxide is the most important parameter in controlling the periodicity of these nanostructures. Herein we demonstrate a simple and yet powerful method to fabricate ordered anodic aluminum oxides with continuously tunable interpore distances. By using mixed solution of citric and oxalic acids with different molar ratio, the range of anodizing voltages within which self-ordered films can be formed were extended to between 40 and 300 V, resulting in the interpore distances change from 100 to 750 nm. Our work realized very broad range of interpore distances in a continuously tunable fashion and the experiment processes are easily controllable and reproducible. The dependence of the interpore distances on acid ratios in mixed solutions was discussed through analysis of anodizing current and it was found that the effective dissociation constant of the mixed acids is of great importance. The interpore distances achieved are comparable to wavelengths ranging from UV to near IR, and may have potential applications in optical meta-materials for photovoltaics and optical sensing.

  13. Fabrication of free standing anodic titanium oxide membranes with clean surface using recycling process.

    PubMed

    Meng, Xianhui; Lee, Tae-Young; Chen, Huiyu; Shin, Dong-Wook; Kwon, Kee-Won; Kwon, Sang Jik; Yoo, Ji-Beom

    2010-07-01

    Large area of self-organized, free standing anodic titanium oxide (ATO) nanotube membranes with clean surfaces were facilely prepared to desired lengths via electrochemical anodization of highly pure Ti sheets in an ethylene glycol electrolyte, with a small amount of NH4F and H2O at 50 V, followed by self-detachment of the ATO membrane from the Ti substrate using recycling processes. In the first anodization step, the nanowire oxide layer existed over the well-arranged ATO nanotube. After sufficiently rinsing with water, the whole ATO layer was removed from the Ti sheet by high pressure N2 gas, and a well-patterned dimple layer with a thickness of about 30 nm existed on the Ti substrate. By using these naturally formed nano-scale pits as templates, in the second and third anodization process, highly ordered, vertically aligned, and free standing ATO membranes with the anodic aluminum oxide (AAO)-like clean surface were obtained. The inter-pore distance and diameter was 154 +/- 2 nm and 91+/- 2 nm, the tube arrays lengths for 25 and 46 hours were 44 and 70 microm, respectively. The present study demonstrates a simple approach to producing high quality, length controllable, large area TiO2 membrane. PMID:21128409

  14. Development of an Inert Anode for Electrowinning in Calcium Chloride-Calcium Oxide Melts

    NASA Astrophysics Data System (ADS)

    Jiao, Shuqiang; Fray, Derek J.

    2010-02-01

    Studies were performed investigating the anodic testing of calcium ruthenate for electrowinning in calcium chloride-calcium oxide melts. The results showed that calcium ruthenate may be suitable as an inert anode in calcium chloride containing melts as it exhibited a low rate of corrosion in melts containing a small amount of calcium oxide, capable of producing oxygen on its surface, and did not contaminate the melt. To reduce the amount of ruthenium in the anode, solid solutions of calcium ruthenate in calcium titanate were investigated. At low concentrations, the solid solution is a semiconductor with a relatively low conductivity at room temperature, but at the temperature of operation, 1173 K, the material is an excellent electronic conductor. The other way of reducing the amount of ruthenium is to coat the solid solution onto a substrate. In this way, the substrate would give the mechanical strength while the coating would give the electrical conductivity and corrosion protection. Calcium ruthenate-based anodes can endure long-term use in the laboratory under an applied electrical field with oxygen being liberated on the anode indicating that these materials are candidates for the electrowining in calcium chloride-calcium oxide melts.

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

    PubMed

    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

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

    SciTech Connect

    Canulescu, S. Schou, J.; Rechendorff, K.; Pleth Nielsen, L.; Borca, C. N.; Jones, N. C.; Hoffmann, S. V.; Bordo, K.; Ambat, R.

    2014-03-24

    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 TiO{sub 2} 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 Al{sub 2}O{sub 3} has a direct band gap of 7.3 eV, which is about ∼1.4 eV lower than its crystalline counterpart (single-crystal Al{sub 2}O{sub 3}). Upon Ti-alloying, extra bands appear within the band gap of amorphous Al{sub 2}O{sub 3}, mainly caused by Ti 3d orbitals localized at the Ti site.

  17. Porous hollow carbon spheres decorated with molybdenum diselenide nanosheets as anodes for highly reversible lithium and sodium storage

    NASA Astrophysics Data System (ADS)

    Yang, Xing; Zhang, Zhian; Fu, Yun; Li, Qiang

    2015-05-01

    Porous hollow carbon spheres (PHCS) decorated with MoSe2 nanosheets (MoSe2@ PHCS) are synthesized via a three-step process. Uniform and conformal MoSe2 nanosheets are firmly attached to PHCS according to the characterization of scanning electron microscopy (SEM), transmission electron microscopy (TEM) and nitrogen adsorption/desorption measurements. Enhanced electrochemical performance of MoSe2@PHCS is investigated in lithium-ion and sodium-ion storage. The MoSe2@PHCS deliver a reversible lithium storage capacity of 681 mA h g-1 for 100 discharge/charge cycles. In Na-ion batteries, it manifests a reversible sodium capacity of 580 mA h g-1 after 100 cycles. Three synergic effects can be attributed to the enhanced electrochemical performance of MoSe2@PHCS: (1) both the sheet structure of the MoSe2 and the mechanically robust carbon sphere supporter can accommodate stress from cycling; (2) the porous hollow carbon spheres matrix in the MoSe2@PHCS offers a beneficial conductivity environment; (3) uniform and conformal MoSe2 nanosheets attachment shortens the electronic lithium-ion and sodium-ion pathway during cycling. The MoSe2@PHCS have a great potential as an anode for lithium and sodium batteries.Porous hollow carbon spheres (PHCS) decorated with MoSe2 nanosheets (MoSe2@ PHCS) are synthesized via a three-step process. Uniform and conformal MoSe2 nanosheets are firmly attached to PHCS according to the characterization of scanning electron microscopy (SEM), transmission electron microscopy (TEM) and nitrogen adsorption/desorption measurements. Enhanced electrochemical performance of MoSe2@PHCS is investigated in lithium-ion and sodium-ion storage. The MoSe2@PHCS deliver a reversible lithium storage capacity of 681 mA h g-1 for 100 discharge/charge cycles. In Na-ion batteries, it manifests a reversible sodium capacity of 580 mA h g-1 after 100 cycles. Three synergic effects can be attributed to the enhanced electrochemical performance of MoSe2@PHCS: (1) both the sheet

  18. Photo-oxidation effects of light-emitting porous Si

    NASA Astrophysics Data System (ADS)

    Tamura, Tomoyuki; Adachi, Sadao

    2009-06-01

    The effects of light illumination on porous silicon (PSi) properties have been studied using photoluminescence (PL), PL excitation (PLE), and x-ray photoelectron spectroscopy (XPS) measurements. The PL spectrum evolution in PSi sample under light illumination at various wavelengths indicates that the photo-oxidation occurs and causes a decrease in its intensity with increasing illumination time t. The decrease in the PL intensity IPL can be written as logarithmic expression, namely, the Elovich equation IPL∝-α ln t, where α is the quenching rate of the PL intensity associated with the native oxide growth. The α value is dependent on the illuminated photon energy Epo in a manner α =0.050Epo. Each PL spectrum can be deconvoluted into four Gaussian peaks. The higher the PL peak energy, the larger its photo-oxidation-induced blueshift. This fact and XPS results support that the light emission in a porous sample is due to the quantum-size effect, i.e., relaxation of the momentum conservation at and above the indirect absorption edge (supra-indirect-gap emission). The PLE spectra suggest that the surface hydrogen termination should influence the highly excited carrier dynamics in nanocrystalline PSi materials.

  19. Synthesis and microstructure of porous Mn-oxides

    NASA Astrophysics Data System (ADS)

    Musić, Svetozar; Ristić, Mira; Popović, Stanko

    2009-04-01

    Porous Mn-oxide particles were synthesized by urea processing in combination with the thermal treatment of the precursor precipitated. The samples were characterized by XRD, FT-IR, DTA, FE-SEM and EDS. Upon heating of the precursor at 600 °C, α-Mn 2O 3 particles containing nanopores (cheese-like) were obtained. Most nanopores varied from ˜20 to 60 nm, and some were close to ˜100 nm in size. The α-Mn 2O 3 particles showed a strong twinning effect. At 1100 °C, Mn 3O 4 particles, obtained as a single crystal phase, formed a microporous 3D structure.

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

    NASA Astrophysics Data System (ADS)

    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.

  1. Reduced graphene oxide anodes for potential application in algae biophotovoltaic platforms.

    PubMed

    Ng, Fong-Lee; Jaafar, Muhammad Musoddiq; Phang, Siew-Moi; Chan, Zhijian; Salleh, Nurul Anati; Azmi, Siti Zulfikriyah; Yunus, Kamran; Fisher, Adrian C; Periasamy, Vengadesh

    2014-01-01

    The search for renewable energy sources has become challenging in the current era, as conventional fuel sources are of finite origins. Recent research interest has focused on various biophotovoltaic (BPV) platforms utilizing algae, which are then used to harvest solar energy and generate electrical power. The majority of BPV platforms incorporate indium tin oxide (ITO) anodes for the purpose of charge transfer due to its inherent optical and electrical properties. However, other materials such as reduced graphene oxide (RGO) could provide higher efficiency due to their intrinsic electrical properties and biological compatibility. In this work, the performance of algae biofilms grown on RGO and ITO anodes were measured and discussed. Results indicate improved peak power of 0.1481 mWm(-2) using the RGO electrode and an increase in efficiency of 119%, illustrating the potential of RGO as an anode material for applications in biofilm derived devices and systems. PMID:25531093

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

    PubMed Central

    2007-01-01

    Self-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

    PubMed Central

    Faes, Antonin; Hessler-Wyser, Aïcha; Zryd, Amédée; Van Herle, Jan

    2012-01-01

    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. PMID:24958298

  4. The application of the barrier-type anodic oxidation method to thickness testing of aluminum films.

    PubMed

    Chen, Jianwen; Yao, Manwen; Xiao, Ruihua; Yang, Pengfei; Hu, Baofu; Yao, Xi

    2014-09-01

    The thickness of the active metal oxide film formed from a barrier-type anodizing process is directly proportional to its formation voltage. The thickness of the consumed portion of the metal film is also corresponding to the formation voltage. This principle can be applied to the thickness test of the metal films. If the metal film is growing on a dielectric substrate, when the metal film is exhausted in an anodizing process, because of the high electrical resistance of the formed oxide film, a sudden increase of the recorded voltage during the anodizing process would occur. Then, the thickness of the metal film can be determined from this voltage. As an example, aluminum films are tested and discussed in this work. This method is quite simple and is easy to perform with high precision. PMID:25273741

  5. The application of the barrier-type anodic oxidation method to thickness testing of aluminum films

    NASA Astrophysics Data System (ADS)

    Chen, Jianwen; Yao, Manwen; Xiao, Ruihua; Yang, Pengfei; Hu, Baofu; Yao, Xi

    2014-09-01

    The thickness of the active metal oxide film formed from a barrier-type anodizing process is directly proportional to its formation voltage. The thickness of the consumed portion of the metal film is also corresponding to the formation voltage. This principle can be applied to the thickness test of the metal films. If the metal film is growing on a dielectric substrate, when the metal film is exhausted in an anodizing process, because of the high electrical resistance of the formed oxide film, a sudden increase of the recorded voltage during the anodizing process would occur. Then, the thickness of the metal film can be determined from this voltage. As an example, aluminum films are tested and discussed in this work. This method is quite simple and is easy to perform with high precision.

  6. Reduced Graphene Oxide Anodes for Potential Application in Algae Biophotovoltaic Platforms

    PubMed Central

    Ng, Fong-Lee; Jaafar, Muhammad Musoddiq; Phang, Siew-Moi; Chan, Zhijian; Salleh, Nurul Anati; Azmi, Siti Zulfikriyah; Yunus, Kamran; Fisher, Adrian C.; Periasamy, Vengadesh

    2014-01-01

    The search for renewable energy sources has become challenging in the current era, as conventional fuel sources are of finite origins. Recent research interest has focused on various biophotovoltaic (BPV) platforms utilizing algae, which are then used to harvest solar energy and generate electrical power. The majority of BPV platforms incorporate indium tin oxide (ITO) anodes for the purpose of charge transfer due to its inherent optical and electrical properties. However, other materials such as reduced graphene oxide (RGO) could provide higher efficiency due to their intrinsic electrical properties and biological compatibility. In this work, the performance of algae biofilms grown on RGO and ITO anodes were measured and discussed. Results indicate improved peak power of 0.1481 mWm−2 using the RGO electrode and an increase in efficiency of 119%, illustrating the potential of RGO as an anode material for applications in biofilm derived devices and systems. PMID:25531093

  7. Acid blue 29 decolorization and mineralization by anodic oxidation with a cold gas spray synthesized Sn-Cu-Sb alloy anode.

    PubMed

    do Vale-Júnior, Edilson; Dosta, Sergi; Cano, Irene Garcia; Guilemany, Josep Maria; Garcia-Segura, Sergi; Martínez-Huitle, Carlos Alberto

    2016-04-01

    The elevated cost of anodic materials used in the anodic oxidation for water treatment of effluents undermines the real application of these technologies. The study of novel alternative materials more affordable is required. In this work, we report the application of Sn-Cu-Sb alloys as cheap anodic material to decolorize azo dye Acid Blue 29 solutions. These anodes have been synthesized by cold gas spray technologies. Almost complete decolorization and COD abatement were attained after 300 and 600 min of electrochemical treatment, respectively. The influence of several variables such as supporting electrolyte, pH, current density and initial pollutant concentration has been investigated. Furthermore, the release and evolution of by-products was followed by HPLC to better understand the oxidative power of Sn-Cu-Sb electrodes. PMID:26802262

  8. Effects of anode fabrication parameters on the performance and redox behavior of solid oxide fuel cells

    NASA Astrophysics Data System (ADS)

    Timurkutluk, Bora; Mat, Mahmut D.

    2014-07-01

    Anode supported solid oxide fuel cells (SOFCs) having various anode support porosities and electrolyte thicknesses are developed and their effects on the cell performance and redox behavior of the cell are investigated experimentally. An yttria stabilized zirconia based anode supported membrane electrode group (MEG) is developed with the tape casting, co-sintering and screen printing methodologies. For comparison, various anode supported cells with different electrolyte thickness and anode support porosities are also fabricated. An experimental setup is devised for the performance measurement of the cells before and after redox cycling. The mechanical performance of the cell before and after redox cycling is also measured via three point bending tests. Experimental results reveal that the porosity of the anode support and the thickness of the electrolyte should be carefully decided by considering not only the cell performances but also the redox stability. In addition, after single redox cycle the decrease in the mechanical properties of the cell is found to be around 50% while the same cell shows only around 10% electrochemical performance loss.

  9. Improved microstructure and performance of Ni-based anode for intermediate temperature solid oxide fuel cells

    NASA Astrophysics Data System (ADS)

    Hua, Bin; Zhang, Wenying; Li, Meng; Wang, Xin; Chi, Bo; Pu, Jian; Li, Jian

    2014-02-01

    Three kinds of anodes prepared by NiO impregnation, (Ni, Mg)O impregnation and conventional sintering methods are investigated under the conditions of anodic current polarization and redox cycling. The optimized NiO loading in the NiO-impregnated anode is 40 wt%; and the minimum polarization resistance is 1.40, 0.71 and 0.60 Ω cm2 at 700, 750 and 800 °C, respectively, due to the increased triple phase boundary and conductivity that promote the charge-transfer process of H2 oxidation reaction. The conventional Ni-YSZ cermet anode is less sensitive to the current polarization at 200 mA cm-2; however, its polarization resistance is much higher than those of the impregnated anodes. (Ni, Mg)O impregnation improves the performance durability and redox-ability at 800 °C, with a low polarization resistance of 0.93 Ω cm2 after 48 h of current polarization and of 0.71 Ω cm2 after 10 redox cycles. The addition of Mg lowers the reducibility of (Ni, Mg)O particles; and its improved electrochemical performance and redox cycling resistance are attributed to its stabilized microstructure consisting of nano-scale Ni particles distributed on the surface of the pre-sintered YSZ scaffold. The agglomeration of fine Ni particles is suppressed by the unreduced (Ni, Mg)O in the anode.

  10. Solid oxide fuel cell anode degradation by the effect of siloxanes

    NASA Astrophysics Data System (ADS)

    Madi, Hossein; Lanzini, Andrea; Diethelm, Stefan; Papurello, Davide; Van herle, Jan; Lualdi, Matteo; Gutzon Larsen, Jørgen; Santarelli, Massimo

    2015-04-01

    Lifetime and durability issues connected with Solid Oxide Fuel Cell (SOFC) technology are strongly related to the amount of contaminants that reach the stack. In this study the focus is on organic silicon compounds (siloxanes) and their highly detrimental effects on the performance of SOFC Ni-YSZ anodes. The involved mechanism of degradation is clarified and quantified through several test runs and subsequent post-mortem analysis on tested samples. In particular, experiments on both Ni anode-supported single cells and 11-cell- stacks are performed, co-feeding D4-siloxane (octamethylcyclotetrasiloxane, C8H24O4Si4) as model compound for the organic silicon species which are generally found in sewage biogas. High degradation rates are observed already at ppb(v) level of contaminant in the fuel stream. Post-test analysis revealed that Si (as silica) is mostly deposited at the inlet of the fuel channel on both the interconnect and the anode side of the cell suggesting a relatively fast condensation-type process. Deposition of the Si was found on the interconnect and on the anode contact layer, throughout the anode support and the three phase boundary in the anode, correlating with the observed increase of polarization losses from the EIS analysis of tested cells.

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

    NASA Technical Reports Server (NTRS)

    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.

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

    NASA Astrophysics Data System (ADS)

    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.

  13. The cooperative electrochemical oxidation of chlorophenols in anode-cathode compartments.

    PubMed

    Wang, Hui; Wang, Jian Long

    2008-06-15

    By using a self-made carbon/polytetrafluoroethylene (C/PTFE) O2-fed as the cathode and Ti/IrO2/RuO2 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 (H2O2) was 8.3 mg/L, and hydroxyl radical (HO) 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 H2O2, HO 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 H2O2, HO 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. PMID:17996367

  14. A redox-stable efficient anode for solid-oxide fuel cells.

    PubMed

    Tao, Shanwen; Irvine, John T S

    2003-05-01

    Solid-oxide fuel cells (SOFCs) promise high efficiencies in a range of fuels. Unlike lower temperature variants, carbon monoxide is a fuel rather than a poison, and so hydrocarbon fuels can be used directly, through internal reforming or even direct oxidation. This provides a key entry strategy for fuel-cell technology into the current energy economy. Present development is mainly based on the yttria-stabilized zirconia (YSZ) electrolyte. The most commonly used anode materials are Ni/YSZ cermets, which display excellent catalytic properties for fuel oxidation and good current collection, but do exhibit disadvantages, such as low tolerance to sulphur and carbon deposition when using hydrocarbon fuels, and poor redox cycling causing volume instability. Here, we report a nickel-free SOFC anode, La0.75Sr0.25Cr0.5Mn0.5O3, with comparable electrochemical performance to Ni/YSZ cermets. The electrode polarization resistance approaches 0.2 Omega cm2 at 900 degrees C in 97% H2/3% H2O. Very good performance is achieved for methane oxidation without using excess steam. The anode is stable in both fuel and air conditions, and shows stable electrode performance in methane. Thus both redox stability and operation in low steam hydrocarbons have been demonstrated, overcoming two of the major limitations of the current generation of nickel zirconia cermet SOFC anodes. PMID:12692533

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

    Technology Transfer Automated Retrieval System (TEKTRAN)

    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...

  16. A Comparison of Molten Sn and Bi for Solid Oxide Fuel Cell Anodes

    SciTech Connect

    Jayakumar, A.; Lee, Sang Bok; Hornés, A.; Vohs, J. M.; Gorte, R. J.

    2010-01-01

    Molten Sn and Bi were examined at 973 and 1073 K for use as anodes in solid oxide fuel cells with yttria-stabilized zirconia (YSZ) electrolytes. Cells were operated under “battery” conditions, with dry He flow in the anode compartment, to characterize the electrochemical oxidation of the metals at the YSZ interface. For both metals, the open-circuit voltages (OCVs) were close to that expected based on their oxidation thermodynamics, ~0.93 V for Sn and ~0.48 V for Bi. With Sn, the cell performance degraded rapidly after the transfer of approximately 0.5-1.5 Ccm{sup 2} of charge due to the formation of a SnO{sub 2} layer at the YSZ interface. At 973 K, the anode impedance at OCV for freshly reduced Sn was approximately 3 {ohm}cm{sup 2} but this increased to well over 250 {ohm}cm{sup 2} after the transfer of of charge. Following the transfer of 8.2 Ccm{sup 2} at 1073 K, the formation of a 10{micro}m thick SnO{sub 2} layer was confirmed by scanning electron microscopy. With Bi, the OCV anode impedance at 973 K was less than 0.25 {ohm}cm{sup 2} and remained constant until essentially all of the Bi had been oxidized to BiO{sub 2}. Some implications of these results for direct carbon fuel cells are discussed.

  17. First Introduction of NiSe2 to Anode Material for Sodium-Ion Batteries: A Hybrid of Graphene-Wrapped NiSe2/C Porous Nanofiber

    PubMed Central

    Cho, Jung Sang; Lee, Seung Yeon; Kang, Yun Chan

    2016-01-01

    The first-ever study of nickel selenide materials as efficient anode materials for Na-ion rechargeable batteries is conducted using the electrospinning process. NiSe2-reduced graphene oxide (rGO)-C composite nanofibers are successfully prepared via electrospinning and a subsequent selenization process. The electrospun nanofibers giving rise to these porous-structured composite nanofibers with optimum amount of amorphous C are obtained from the polystyrene to polyacrylonitrile ratio of 1/4. These composite nanofibers also consist of uniformly distributed single-crystalline NiSe2 nanocrystals that have a mean size of 27 nm. In contrast, the densely structured bare NiSe2 nanofibers formed via selenization of the pure NiO nanofibers consist of large crystallites. The initial discharge capacities of the NiSe2-rGO-C composite and bare NiSe2 nanofibers at a current density of 200 mA g−1 are 717 and 755 mA h g−1, respectively. However, the respective 100th-cycle discharge capacities of the former and latter are 468 and 35 mA h g−1. Electrochemical impedance spectroscopy measurements reveal the structural stability of the composite nanofibers during repeated Na-ion insertion and extraction processes. The excellent Na-ion storage properties of these nanofibers are attributed to this structural stability. PMID:26997350

  18. First Introduction of NiSe2 to Anode Material for Sodium-Ion Batteries: A Hybrid of Graphene-Wrapped NiSe2/C Porous Nanofiber

    NASA Astrophysics Data System (ADS)

    Cho, Jung Sang; Lee, Seung Yeon; Kang, Yun Chan

    2016-03-01

    The first-ever study of nickel selenide materials as efficient anode materials for Na-ion rechargeable batteries is conducted using the electrospinning process. NiSe2-reduced graphene oxide (rGO)-C composite nanofibers are successfully prepared via electrospinning and a subsequent selenization process. The electrospun nanofibers giving rise to these porous-structured composite nanofibers with optimum amount of amorphous C are obtained from the polystyrene to polyacrylonitrile ratio of 1/4. These composite nanofibers also consist of uniformly distributed single-crystalline NiSe2 nanocrystals that have a mean size of 27 nm. In contrast, the densely structured bare NiSe2 nanofibers formed via selenization of the pure NiO nanofibers consist of large crystallites. The initial discharge capacities of the NiSe2-rGO-C composite and bare NiSe2 nanofibers at a current density of 200 mA g‑1 are 717 and 755 mA h g‑1, respectively. However, the respective 100th-cycle discharge capacities of the former and latter are 468 and 35 mA h g‑1. Electrochemical impedance spectroscopy measurements reveal the structural stability of the composite nanofibers during repeated Na-ion insertion and extraction processes. The excellent Na-ion storage properties of these nanofibers are attributed to this structural stability.

  19. First Introduction of NiSe2 to Anode Material for Sodium-Ion Batteries: A Hybrid of Graphene-Wrapped NiSe2/C Porous Nanofiber.

    PubMed

    Cho, Jung Sang; Lee, Seung Yeon; Kang, Yun Chan

    2016-01-01

    The first-ever study of nickel selenide materials as efficient anode materials for Na-ion rechargeable batteries is conducted using the electrospinning process. NiSe2-reduced graphene oxide (rGO)-C composite nanofibers are successfully prepared via electrospinning and a subsequent selenization process. The electrospun nanofibers giving rise to these porous-structured composite nanofibers with optimum amount of amorphous C are obtained from the polystyrene to polyacrylonitrile ratio of 1/4. These composite nanofibers also consist of uniformly distributed single-crystalline NiSe2 nanocrystals that have a mean size of 27 nm. In contrast, the densely structured bare NiSe2 nanofibers formed via selenization of the pure NiO nanofibers consist of large crystallites. The initial discharge capacities of the NiSe2-rGO-C composite and bare NiSe2 nanofibers at a current density of 200 mA g(-1) are 717 and 755 mA h g(-1), respectively. However, the respective 100(th)-cycle discharge capacities of the former and latter are 468 and 35 mA h g(-1). Electrochemical impedance spectroscopy measurements reveal the structural stability of the composite nanofibers during repeated Na-ion insertion and extraction processes. The excellent Na-ion storage properties of these nanofibers are attributed to this structural stability. PMID:26997350

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

    NASA Astrophysics Data System (ADS)

    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.

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

    PubMed

    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. PMID:27070754

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

    NASA Astrophysics Data System (ADS)

    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.

  3. X-ray absorption spectroscopy from H-passivated porous Si and oxidized Si nanocrystals

    SciTech Connect

    Schuppler, S.; Marcus, M.A.; Friedman, S.L.

    1994-11-01

    Quantum confinement in nanoscale Si structures is widely believed to be responsible for the visible luminescence observed from anodically etched porous silicon (por-Si), but little is known about the actual size or shape of these structures. Extended x-ray absorption fine structure data from a wide variety of por-Si samples show significantly reduced average Si coordination numbers due to the sizable contribution of surface-coordinated H. (The IUSI ratios, as large as 1.2, were independently confirmed by ir-absorption and {alpha}-recoil measurements.) The Si coordinations imply very large surface/volume ratios, enabling the average Si structures to be identified as crystalline particles (not wires) whose dimensions are typically <15 {Angstrom}. Comparison of the size-dependent peak luminescence energies with those of oxidized Si nanocrystals, whose shapes are known, shows remarkable agreement. Furthermore, near-edge x-ray absorption fine structure measurements of the nanocrystals shows the outer oxide and interfacial suboxide layers to be constant over a wide range of nanocrystal sizes. The combination of these results effectively rules out surface species as being responsible for the observed visible luminescence in por-Si, and strongly supports quantum confinement as the dominant mechanism occurring in Si particles which are substantially smaller than previously reported or proposed.

  4. A three-dimensional porous MoP@C hybrid as a high-capacity, long-cycle life anode material for lithium-ion batteries.

    PubMed

    Wang, Xia; Sun, Pingping; Qin, Jinwen; Wang, Jianqiang; Xiao, Ying; Cao, Minhua

    2016-05-21

    Metal phosphides are great promising anode materials for lithium-ion batteries with a high gravimetric capacity. However, significant challenges such as low capacity, fast capacity fading and poor cycle stability must be addressed for their practical applications. Herein, we demonstrate a versatile strategy for the synthesis of a novel three-dimensional porous molybdenum phosphide@carbon hybrid (3D porous MoP@C hybrid) by a template sol-gel method followed by an annealing treatment. The resultant hybrid exhibits a 3D interconnected ordered porous structure with a relatively high surface area. Benefiting from its advantages of microstructure and composition, the 3D porous MoP@C hybrid displays excellent lithium storage performance as an anode material for lithium-ion batteries in terms of specific capacity, cycling stability and long-cycle life. It presents stable cycling performance with a high reversible capacity up to 1028 mA h g(-1) at a current density of 100 mA g(-1) after 100 cycles. By ex situ XRD, HRTEM, SAED and XPS analyses, the 3D porous MoP@C hybrid was found to follow the Li-intercalation reaction mechanism (MoP + xLi(+) + e(-)↔ LixMoP), which was further confirmed by ab initio calculations based on density functional theory. PMID:27136974

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

    NASA Astrophysics Data System (ADS)

    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.

  6. Synthesis and characterization of nanoporous anodic oxide film on aluminum in H3PO4 + KMnO4 electrolyte mixture at different anodization conditions

    NASA Astrophysics Data System (ADS)

    Verma, Naveen; Jindal, Jitender; Singh, Krishan Chander; Mari, Bernabe

    2016-04-01

    The micro structural properties of nanoporous anodic oxide film formed in H3PO4 were highly influenced by addition of a low concentration of KMnO4 (0.0005 M) in 1 M H3PO4 solution. The KMnO4 as additive enhanced the growth rate of oxide film formation as well as thickness of pore walls. Furthermore the growth rate was found increased with increase in applied current density. The increase in temperature and lack of stirring during anodization causes the thinness of pore wall which leads to increase in pore volume. With the decrease in concentration of H3PO4 in anodizing electrolyte from 1M to 0.3 M, keeping all other conditions constant, the decrease in porosity was observed. This might be due to the dissolution of aluminium oxide film in highly concentrated acidic solution.

  7. Ti-doped molybdenum-based perovskites as anodes for solid oxide fuel cells

    NASA Astrophysics Data System (ADS)

    He, Beibei; Wang, Zhenbin; Zhao, Ling; Pan, Xin; Wu, Xiaojun; Xia, Changrong

    2013-11-01

    Ti doping is found to increase the stability of Sr2NiMoO6 perovskite oxides in reducing atmosphere. The composition Sr2TiNi0.5Mo0.5O6 (STNM) is further evaluated as a potential oxide anode for solid oxide fuel cells (SOFCs). Electrical conductivity, thermal expansion coefficient, surface exchange coefficient, chemical diffusion coefficient, and its electrochemical performance in single cells with La0.8Sr0.2Ga0.8Mg0.2O3-δ (LSGM) electrolytes are investigated. STNM exhibits a high conductivity of 17.5 S cm-1 at 800 °C at anodic atmosphere. The material shows good chemical and thermal expansion compatibilities with LSGM. To investigate the effect of Ti doping on the conduction properties, first-principle calculations are performed using the Vienna Ab initio Simulation. The strong Ti-O bond is held responsible for the enhanced structural stability of STNM under humidified H2 atmospheres, relative to that of the undoped system. The remarkable cell performance with both H2 and dry CH4 as the fuel indicates the potential ability of STNM to be used as SOFC anodes. These results obtained indicate that Sr2TiNi0.5Mo0.5O6 is a promising material for use as anode for intermediate temperature SOFCs.

  8. Fabrication, Characterization and Application of Metal-oxide Tunnel Junctions by Anodization

    NASA Astrophysics Data System (ADS)

    Fan, Wenbin

    Metal oxides have become of significant interest due to their wide range of electrical properties showing potential applications to next generation memory and logic devices. Recent advances in oxide growth technology and the discovery of some unique properties of metal oxides have led to a renewed potential for novel device functionality. Electrochemical anodization offers an effective means to produce oxides in terms of cost, convenience and purity. In this dissertation, Reactive Bias Target Ion Beam Deposition (RBTIBD) system and electrochemical anodization have been used to fabricate granular nano-structured metal-oxide lateral junctions based on the transition metals, particularly, vanadium (V) and tantalum (Ta). The electrical transport properties of anodized V and Ta metal-oxide junctions were investigated at various temperatures. The results turned out that these junctions all had very non-linear I-V characteristics indicating tunneling-like behaviors. Anodized Ta junction shown an appreciable non- linear behavior of the temperature-dependent I-V characteristic with a resistance change of nearly two orders of magnitude at T-300K at currents between 0 and 0.1 mA (˜ 1.3x104 A/cm2 or 104 V/cm). The metal-insulator-transition (MIT) was observed in both wire and bulk V junctions at ˜ 80°C. The microstructure of these anodized transition metal films was characterized by Transmission Electron Microscope (TEM), which was consistent with metallic grains embedded in an oxide matrix. Therefore an anodized granular metal film could be treated as a tunnel junction network. Two dominant electron conduction mechanisms were clearly identified by fitting the I(V, T) data of a Ta oxide- metal junction. The first mechanism was a temperature-independent tunneling including F-N and direct tunneling. The second mechanism was the modified temperature-dependent 2-dimentional Mott's variable-range hopping (VRH) model. The classical Simmons' equation was used to quantify the

  9. Electrodeposited three-dimensional porous Si-O-C/Ni thick film as high performance anode for lithium-ion batteries

    NASA Astrophysics Data System (ADS)

    Qian, Xin; Hang, Tao; Nara, Hiroki; Yokoshima, Tokihiko; Li, Ming; Osaka, Tetsuya

    2014-12-01

    A novel 3D porous Si-O-C/Ni thick film anode is successfully prepared by electrodeposition of porous Ni on Cu substrate and galvanostatical electrodeposition of Si-O-C composite on porous Ni substrate. The 3D porous Si-O-C/Ni thick film is electrochemically activated at a current density of 50 μA cm-2 for the first cycle and 200 μA cm-2 (0.5 C) for the subsequent cycles, it displays superior electrochemical performance with discharge capacity of 706.3 mAh g-1 of Si after 100 cycles. The properties of this thick film is analyzed by field emission scanning electron microscopy (FESEM) and scanning transmission electron microscopy with energy dispersive X-ray analyzer (STEM-EDX). The results show that Si-O-C composite not only covers the surface area of porous Ni but also attaches to the highly porous dendritic walls, along with the porous structure of Ni which provides proper accommodation for the volume change of silicon during the lithiation/delithiation processes, are believed to result in the high capacity and excellent cyclability.

  10. Growth of aluminum-free porous oxide layers on titanium and its alloys Ti-6Al-4V and Ti-6Al-7Nb by micro-arc oxidation.

    PubMed

    Duarte, Laís T; Bolfarini, Claudemiro; Biaggio, Sonia R; Rocha-Filho, Romeu C; Nascente, Pedro A P

    2014-08-01

    The growth of oxides on the surfaces of pure Ti and two of its ternary alloys, Ti-6Al-4V and Ti-6Al-7Nb, by micro-arc oxidation (MAO) in a pH 5 phosphate buffer was investigated. The primary aim was to form thick, porous, and aluminum-free oxide layers, because these characteristics favor bonding between bone and metal when the latter is implanted in the human body. On Ti, Ti-6Al-4 V, and Ti-6Al-7Nb, the oxides exhibited breakdown potentials of about 200 V, 130 V, and 140 V, respectively, indicating that the oxide formed on the pure metal is the most stable. The use of the MAO procedure led to the formation of highly porous oxides, with a uniform distribution of pores; the pores varied in size, depending on the anodizing applied voltage and time. Irrespective of the material being anodized, Raman analyses allowed us to determine that the oxide films consisted mainly of the anatase phase of TiO2, and XPS results indicated that this oxide is free of Al and any other alloying element. PMID:24907769

  11. A new anode material for oxygen evolution in molten oxide electrolysis.

    PubMed

    Allanore, Antoine; Yin, Lan; Sadoway, Donald R

    2013-05-16

    Molten oxide electrolysis (MOE) is an electrometallurgical technique that enables the direct production of metal in the liquid state from oxide feedstock, and compared with traditional methods of extractive metallurgy offers both a substantial simplification of the process and a significant reduction in energy consumption. MOE is also considered a promising route for mitigation of CO2 emissions in steelmaking, production of metals free of carbon, and generation of oxygen for extra-terrestrial exploration. Until now, MOE has been demonstrated using anode materials that are consumable (graphite for use with ferro-alloys and titanium) or unaffordable for terrestrial applications (iridium for use with iron). To enable metal production without process carbon, MOE requires an anode material that resists depletion while sustaining oxygen evolution. The challenges for iron production are threefold. First, the process temperature is in excess of 1,538 degrees Celsius (ref. 10). Second, under anodic polarization most metals inevitably corrode in such conditions. Third, iron oxide undergoes spontaneous reduction on contact with most refractory metals and even carbon. Here we show that anodes comprising chromium-based alloys exhibit limited consumption during iron extraction and oxygen evolution by MOE. The anode stability is due to the formation of an electronically conductive solid solution of chromium(iii) and aluminium oxides in the corundum structure. These findings make practicable larger-scale evaluation of MOE for the production of steel, and potentially provide a key material component enabling mitigation of greenhouse-gas emissions while producing metal of superior metallurgical quality. PMID:23657254

  12. Cerium-modified doped strontium titanate compositions for solid oxide fuel cell anodes and electrodes for other electrochemical devices

    DOEpatents

    Marina, Olga A [Richland, WA; Stevenson, Jeffry W [Richland, WA

    2010-03-02

    The present invention provides novel compositions that find advantageous use in making electrodes for electrochemical cells and electrochemical devices such as solid oxide fuel cells, electrolyzers, sensors, pumps and the like, the compositions comprising cerium-modified doped strontium titanate. The invention also provides novel methods for making and using anode material compositions and solid oxide fuel cells and solid oxide fuel cell assemblies having anodes comprising the compositions.

  13. Cerium-modified doped strontium titanate compositions for solid oxide fuel cell anodes and electrodes for other electrochemical devices

    DOEpatents

    Marina, Olga A [Richland, WA; Stevenson, Jeffry W [Richland, WA

    2010-11-23

    The present invention provides novel compositions that find advantageous use in making electrodes for electrochemical cells and electrochemical devices such as solid oxide fuel cells, electrolyzers, sensors, pumps and the like, the compositions comprising cerium-modified doped strontium titanate. The invention also provides novel methods for making and using anode material compositions and solid oxide fuel cells and solid oxide fuel cell assemblies having anodes comprising the compositions.

  14. An ultra-fast fabrication technique for anode support solid oxide fuel cells by microwave

    NASA Astrophysics Data System (ADS)

    Jiao, Zhenjun; Shikazono, Naoki; Kasagi, Nobuhide

    An effective and facile technique has been developed for high temperature anode-electrolyte co-sintering of anode support solid oxide fuel cells by using microwave activated sparking plasma. A high sintering temperature of 1600 °C can be achieved in a few minutes time by discharging effect. Anode support substrate pellet is uniaxially pressed, and then dip-coated with a 10 μm yttria stabilized zirconia electrolyte layer. After the microwave co-sintering, La 0.8Sr 0.2MnO x cathode is screen-printed onto electrolyte and sintered by conventional thermal method. The cell has stably operated in 3% humidified hydrogen for more than 130 h.

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

    NASA Astrophysics Data System (ADS)

    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.

  16. Long-term testing of in-situ cerium oxide coated anodes for aluminum electrowinning

    SciTech Connect

    King, H.L.

    1989-10-01

    The ELTECH Anode Phase 2 Project (Contract Number AC07-86ID12655), as supported by the Department of Energy (DOE) from December 1988 through April 1989, focused on long-term testing of in-situ anodically deposited cerium oxide (CEROX) coatings on nickel ferrite/Cu cermets. The specific objective of this research was to determine the effectiveness of the CEROX coating in reducing the transfer of cermet components to the produced aluminum. A dosing regimen was first established for the minimum addition of cerium to the cell necessary to produce targeted CEROX coatings on the cermet anode and the periodic additions necessary to maintain coating thicknesses. The effects of the addition of CeF{sub 3} on CEROX coating formation was evaluated for targeted coating thicknesses at three different current densities. Analytical procedures were identified for determining alumina concentrations and the cryolite bath ratio for quasi-commercial baths.

  17. Electro-oxidation of As(III) with dimensionally-stable and conductive-diamond anodes.

    PubMed

    Lacasa, Engracia; Cañizares, Pablo; Rodrigo, Manuel A; Fernández, Francisco J

    2012-02-15

    In this work, arsenic oxidation by an electrochemical process was studied in a batch bench-scale electrolysis plant equipped with mono- and bi-compartment cells, dimensionally-stable anodes (DSAs) and conductive-diamond anodes (CDAs). The results demonstrate that the electrolysis is an adequate technology to transform As(III) into As(V) species, which is an important pre-treatment stage for removing of arsenic from water using technologies such as coagulation or electro-coagulation. The process requires large current densities in non-divided cells to obtain a good As(V)/As(III) ratio, but it can be more efficiently performed at low current densities in cells divided by cationic membranes. The presence of chlorides or sulphates can significantly affect the results due to the formation of powerful oxidants that contribute to the net oxidation process. PMID:22188787

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

    PubMed

    Murugananthan, M; Yoshihara, S; Rakuma, T; Shirakashi, T

    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 (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 12.8x10(-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. PMID:18023975

  19. Binder-free graphene and manganese oxide coated carbon felt anode for high-performance microbial fuel cell.

    PubMed

    Zhang, Changyong; Liang, Peng; Yang, Xufei; Jiang, Yong; Bian, Yanhong; Chen, Chengmeng; Zhang, Xiaoyuan; Huang, Xia

    2016-07-15

    A novel anode was developed by coating reduced graphene oxide (rGO) and manganese oxide (MnO2) composite on the carbon felt (CF) surface. With a large surface area and excellent electrical conductivity, this binder-free anode was found to effectively enhance the enrichment and growth of electrochemically active bacteria and facilitate the extracellular electron transfer from the bacteria to the anode. A microbial fuel cell (MFC) equipped with the rGO/MnO2/CF anode delivered a maximum power density of 2065mWm(-2), 154% higher than that with a bare CF anode. The internal resistance of the MFC with this novel anode was 79Ω, 66% lower than the regular one's (234Ω). Cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) analyses affirmed that the rGO/MnO2 composite significantly increased the anodic reaction rates and facilitated the electron transfer from the bacteria to the anode. The findings from this study suggest that the rGO/MnO2/CF anode, fabricated via a simple dip-coating and electro-deposition process, could be a promising anode material for high-performance MFC applications. PMID:26918615

  20. Nonfilling carbon coating of porous silicon micrometer-sized particles for high-performance lithium battery anodes.

    PubMed

    Lu, Zhenda; Liu, Nian; Lee, Hyun-Wook; Zhao, Jie; Li, Weiyang; Li, Yuzhang; Cui, Yi

    2015-03-24

    Silicon is widely recognized as one of the most promising anode materials for lithium-ion batteries due to its 10 times higher specific capacity than graphite. Unfortunately, the large volume change of Si materials during their lithiation/delithiation process results in severe pulverization, loss of electrical contact, unstable solid-electrolyte interphase (SEI), and eventual capacity fading. Although there has been tremendous progress to overcome these issues through nanoscale materials design, improved volumetric capacity and reduced cost are still needed for practical application. To address these issues, we design a nonfilling carbon-coated porous silicon microparticle (nC-pSiMP). In this structure, porous silicon microparticles (pSiMPs) consist of many interconnected primary silicon nanoparticles; only the outer surface of the pSiMPs was coated with carbon, leaving the interior pore structures unfilled. Nonfilling carbon coating hinders electrolyte penetration into the nC-pSiMPs, minimizes the electrode-electrolyte contact area, and retains the internal pore space for Si expansion. SEI formation is mostly limited to the outside of the microparticles. As a result, the composite structure demonstrates excellent cycling stability with high reversible specific capacity (∼1500 mAh g(-1), 1000 cycles) at the rate of C/4. The nC-pSiMPs contain accurate void space to accommodate Si expansion while not losing packing density, which allows for a high volumetric capacity (∼1000 mAh cm(-3)). The areal capacity can reach over 3 mAh cm(-2) with the mass loading 2.01 mg cm(-2). Moreover, the production of nC-pSiMP is simple and scalable using a low-cost silicon monoxide microparticle starting material. PMID:25738223

  1. A novel porous coral-like Zn0.5Ni0.5Co2O4 as an anode material for lithium ion batteries with excellent rate performance

    NASA Astrophysics Data System (ADS)

    Song, Xiong; Ru, Qiang; Mo, Yudi; Guo, Lingyun; Hu, Shejun; An, Bonan

    2014-12-01

    A novel porous coral-like Zn0.5Ni0.5Co2O4 (ZNCO) is prepared by a facile co-precipitation method using oxalic acid as complex agent, and the ZnCo2O4 (ZCO) nanospheres and NiCo2O4 (NCO) nanoflakes are also prepared for comparison. The obtained products are systematically characterized by powder X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), and X-ray photoelectron spectroscopy (XPS). The results demonstrate that the controlled metallic elements doping has significant effects on the nanostructure and electrochemical performance of the samples. Compared with the ZCO nanospheres and NCO nanoflakes, the coral-like ZNCO materials with enough free space as anodes in lithium ion batteries (LIBs) exhibit a high initial coulombic efficiency of 84%, a high specific capacity of ∼1445 mAh g-1 at a current rate of 100 mA g-1 after 50 cycles, and ∼730 mAh g-1 at a current rate of 1500 mA g-1 after 200 cycles, as well as an excellent rate capability at elevated current rates, such as, ∼1080 and ∼425 mAh g-1 at current rates of 500 and 6000 mA g-1, respectively. This work presents a meaningful way for the preparation of mixed metal oxides with porous nanostructure as superior anodes for lithium ion batteries.

  2. Metal-organic framework derived porous CuO/Cu2O composite hollow octahedrons as high performance anode materials for sodium ion batteries.

    PubMed

    Zhang, Xiaojie; Qin, Wei; Li, Dongsheng; Yan, Dong; Hu, Bingwen; Sun, Zhuo; Pan, Likun

    2015-11-25

    Porous CuO/Cu2O composite hollow octahedrons were synthesized simply by annealing Cu-based metal-organic framework templates. When evaluated as anode materials for sodium ion batteries, they exhibit a high maximum reversible capacity of 415 mA h g(-1) after 50 cycles at 50 mA g(-1) with excellent cycling stability and good rate capability. PMID:26412211

  3. Optimization of Ni-YSZ solid oxide fuel cell anodes by surface laser melting

    NASA Astrophysics Data System (ADS)

    Cubero, A.; Peña, J. I.; Laguna-Bercero, M. A.

    2015-04-01

    A cermet composed of a metallic component (nickel) and a ceramic matrix (yttria stabilized zirconia) is commonly used as the anode for solid oxide fuel cells (SOFC). In the present work we intend to improve the performance of Ni-YSZ anodes by surface laser melting. Symmetrical cells, consisting of two NiO-YSZ anodes (∼20 μm thickness) separated by a relatively thin YSZ electrolyte (∼500 μm) were fabricated by convectional ceramic techniques. Subsequently, laser melting treatments of both anodes were performed using a CO2 laser system, producing a NiO-YSZ eutectic lamellar microstructure. Laser power of 100 W and processing rates of 1 mm s-1 were determined as the optimum processing conditions. Symmetrical processed plates (eutectic sample) were electrically characterized by impedance spectroscopy (EIS), and the results were compared with non-processed plates (ceramic sample). Preliminary EIS results showed that the polarization resistance at higher temperatures (in the range of 900 °C) is about 0.5 Ω cm2 for both the eutectic and the ceramic sample. However, at lower temperatures (in the range of 800 °C) the polarization resistance for both samples differs considerably (2.9 and 1.6 Ω cm2 for the ceramic and eutectic sample, respectively). These experiments confirmed that optimization of the microstructure by laser surface treatment plays a crucial role in the electrochemical properties of the anode cermets.

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

    PubMed

    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. PMID:26999479

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

    NASA Astrophysics Data System (ADS)

    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.

  6. Ceramic Lithium Ion Conductor to Solve the Anode Coking Problem of Practical Solid Oxide Fuel Cells.

    PubMed

    Wang, Wei; Wang, Feng; Chen, Yubo; Qu, Jifa; Tadé, Moses O; Shao, Zongping

    2015-09-01

    For practical solid oxide fuel cells (SOFCs) operated on hydrocarbon fuels, the facile coke formation over Ni-based anodes has become a key factor that limits their widespread application. Modification of the anodes with basic elements may effectively improve their coking resistance in the short term; however, the easy loss of basic elements by thermal evaporation at high temperatures is a new emerging problem. Herein, we propose a new design to develop coking-resistant and stable SOFCs using Li(+) -conducting Li0.33 La0.56 TiO3 (LLTO) as an anode component. In the Ni/LLTO composite, any loss of surface lithium can be efficiently compensated by lithium diffused from the LLTO bulk under operation. Therefore, the SOFC with the Ni/LLTO anode catalyst layer yields excellent power outputs and operational stability. Our results suggest that the simple adoption of a Li(+) conductor as a modifier for Ni-based anodes is a practical and easy way to solve the coking problem of SOFCs that operate on hydrocarbons. PMID:25925556

  7. Building robust architectures of carbon and metal oxide nanocrystals toward high-performance anodes for lithium-ion batteries.

    PubMed

    Jia, Xilai; Chen, Zheng; Cui, Xia; Peng, Yiting; Wang, Xiaolei; Wang, Ge; Wei, Fei; Lu, Yunfeng

    2012-11-27

    Design and fabrication of effective electrode structure is essential but is still a challenge for current lithium-ion battery technology. Herein we report the design and fabrication of a class of high-performance robust nanocomposites based on iron oxide spheres and carbon nanotubes (CNTs). An efficient aerosol spray process combined with vacuum filtration was used to synthesize such composite architecture, where oxide nanocrystals were assembled into a continuous carbon skeleton and entangled in porous CNT networks. This material architecture offers many critical features that are required for high-performance anodes, including efficient ion transport, high conductivity, and structure durability, therefore enabling an electrode with outstanding lithium storage performance. For example, such an electrode with a thickness of ∼35 μm could deliver a specific capacity of 994 mA h g(-1) (based on total electrode weight) and high recharging rates. This effective strategy can be extended to construct many other composite electrodes for high-performance lithium-ion batteries. PMID:23046380

  8. Nitrogen-Enriched Porous Carbon Coating for Manganese Oxide Nanostructures toward High-Performance Lithium-Ion Batteries.

    PubMed

    Wang, Jiangan; Zhang, Cunbao; Kang, Feiyu

    2015-05-01

    Manganese oxides are promising high-capacity anode materials for lithium-ion batteries (LIBs) yet suffer from short cycle life and poor rate capability. Herein, we demonstrate a facile in situ interfacial synthesis of core-shell heterostructures comprising nitrogen-enriched porous carbon (pN-C) nanocoating and manganese oxide (MnOx) nanotubes. When MnOx/pN-C serves as an anode material for LIBs, the pN-C coating plays multiple roles in substantially improving the lithium storage performance. In combination with the nanosized structure and nanotubular architecture, the MnOx/pN-C nanocomposites exhibit an impressive reversible capacity of 1068 mAh g(-1) at 100 mA g(-1), a high-rate delivery of 361 mAh g(-1) at 8 A g(-1), and a stable cycling retention up to 300 cycles. The surface pN-C coating strategy can be extended to design and fabricate various metal oxide nanostructures for high-performance LIBs. PMID:25871883

  9. Invariance of the mobility edge in anodic titanium oxides

    NASA Astrophysics Data System (ADS)

    Tit, N.; Halley, J. W.; Shore, H. B.

    1992-05-01

    A theoretical investigation to explain the electronic and optical properties of anodic rutile TiO2 thin films of different thicknesses (ranging from 5nm to 20nm) is described. There is experimental evidence that the observed gap state at 0.7eV below the edge of conduction-band is due to an oxygen vacancy. For this reason, oxygen vacancies are used as defects in our model. A comparison of the calculated bulk-photoconductivity to photospectroscopy experiment reveals that the films have bulk-like transport properties with a bandgap E(sub g) = 3.0 eV. On the other hand, a fit of the surface density of states to the scanning tunneling microscopy (STM) experiment on the (001) surfaces has suggested a surface defect density of 5% of oxygen vacancies. To resolve this discrepancy, the dc-conductivity where localization effects are included was calculated. Our results show an impurity band formation at about p(sub c) = 9% of oxygen vacancies. It was concluded that the studied films have defect densities below the threshold of impurity band formation. As a consequence the gap states seen in STM are localized (i.e. the oxygen vacancies are playing the role of trapping centers, deep levels) and the mobility edge is invariant.

  10. Invariance of the Mobility Edge in Anodic Titanium Oxides

    NASA Astrophysics Data System (ADS)

    Tit, Nacir; Halley, J. W.; Shore, H. B.

    We present a theoretical investigation to explain the electronic and optical properties of anodic rutile TiO2 thin films of different thicknesses (ranging from 5nm to 20nm). There is experimental evidence that the observed gap state at 0.7eV below the edge of conduction-band is due to an oxygen vacancy. For this reason, oxygen vacancies are used as defects in our model. A comparison of the calculated bulk-photoconductivity to photospectroscopy experiment reveals that the films have bulk-like transport properties with a bandgap Eg = 3.0eV. On the other hand, a fit of the surface density of states to the scanning tunneling microscopy (STM) experiment on the (001) surfaces has suggested a surface defect density of 5% of oxygen vacancies. To resolve this discrepancy, we calculated the dc-conductivity where localization effects are included. Our results show an impurity band formation at about pc = 9% of oxygen vacancies. We concluded that the studied films have defect densities below the threshold of impurity band formation. As a consequence the gap states seen in STM are localized (i.e: the oxygen vacancies are playing the role of trapping centers, deep levels) and the mobility edge is invariant.

  11. Effect of Graphene Oxide on the Properties of Porous Silicon.

    PubMed

    Olenych, Igor B; Aksimentyeva, Olena I; Monastyrskii, Liubomyr S; Horbenko, Yulia Yu; Partyka, Maryan V; Luchechko, Andriy P; Yarytska, Lidia I

    2016-12-01

    We studied an effect of the graphene oxide (GO) layer on the optical and electrical properties of porous silicon (PS) in hybrid PS-GO structure created by electrochemical etching of silicon wafer and deposition of GO from water dispersion on PS. With the help of scanning electron microscopy (SEM), atomic-force microscopy (AFM), and Fourier transform infrared (FTIR) spectroscopy, it was established that GO formed a thin film on the PS surface and is partly embedded in the pores of PS. A comparative analysis of the FTIR spectra for the PS and PS-GO structures confirms the passivation of the PS surface by the GO film. This film has a sufficient transparency for excitation and emission of photoluminescence (PL). Moreover, GO modifies PL spectrum of PS, shifting the PL maximum by 25 nm towards lower energies. GO deposition on the surface of the porous silicon leads to the change in the electrical parameters of PS in AC and DC modes. By means of current-voltage characteristics (CVC) and impedance spectroscopy, it is shown that the impact of GO on electrical characteristics of PS manifests in reduced capacitance and lower internal resistance of hybrid structures. PMID:26831681

  12. Effect of Graphene Oxide on the Properties of Porous Silicon

    NASA Astrophysics Data System (ADS)

    Olenych, Igor B.; Aksimentyeva, Olena I.; Monastyrskii, Liubomyr S.; Horbenko, Yulia Yu.; Partyka, Maryan V.; Luchechko, Andriy P.; Yarytska, Lidia I.

    2016-02-01

    We studied an effect of the graphene oxide (GO) layer on the optical and electrical properties of porous silicon (PS) in hybrid PS-GO structure created by electrochemical etching of silicon wafer and deposition of GO from water dispersion on PS. With the help of scanning electron microscopy (SEM), atomic-force microscopy (AFM), and Fourier transform infrared (FTIR) spectroscopy, it was established that GO formed a thin film on the PS surface and is partly embedded in the pores of PS. A comparative analysis of the FTIR spectra for the PS and PS-GO structures confirms the passivation of the PS surface by the GO film. This film has a sufficient transparency for excitation and emission of photoluminescence (PL). Moreover, GO modifies PL spectrum of PS, shifting the PL maximum by 25 nm towards lower energies. GO deposition on the surface of the porous silicon leads to the change in the electrical parameters of PS in AC and DC modes. By means of current-voltage characteristics (CVC) and impedance spectroscopy, it is shown that the impact of GO on electrical characteristics of PS manifests in reduced capacitance and lower internal resistance of hybrid structures.

  13. Air Flow and Pressure Drop Measurements Across Porous Oxides

    NASA Technical Reports Server (NTRS)

    Fox, Dennis S.; Cuy, Michael D.; Werner, Roger A.

    2008-01-01

    This report summarizes the results of air flow tests across eight porous, open cell ceramic oxide samples. During ceramic specimen processing, the porosity was formed using the sacrificial template technique, with two different sizes of polystyrene beads used for the template. The samples were initially supplied with thicknesses ranging from 0.14 to 0.20 in. (0.35 to 0.50 cm) and nonuniform backside morphology (some areas dense, some porous). Samples were therefore ground to a thickness of 0.12 to 0.14 in. (0.30 to 0.35 cm) using dry 120 grit SiC paper. Pressure drop versus air flow is reported. Comparisons of samples with thickness variations are made, as are pressure drop estimates. As the density of the ceramic material increases the maximum corrected flow decreases rapidly. Future sample sets should be supplied with samples of similar thickness and having uniform surface morphology. This would allow a more consistent determination of air flow versus processing parameters and the resulting porosity size and distribution.

  14. Uniform Incorporation of Flocculent Molybdenum Disulfide Nanostructure into Three-Dimensional Porous Graphene as an Anode for High-Performance Lithium Ion Batteries and Hybrid Supercapacitors.

    PubMed

    Zhang, Fan; Tang, Yongbing; Liu, Hui; Ji, Hongyi; Jiang, Chunlei; Zhang, Jing; Zhang, Xiaolong; Lee, Chun-Sing

    2016-02-01

    Hybrid supercapacitors (HSCs) with lithium-ion battery-type anodes and electric double layer capacitor-type cathodes are attracting extensive attention and under wide investigation because of their combined merits of both high power and energy density. However, the performance of most HSCs is limited by low kinetics of the battery-type anode which cannot match the fast kinetics of the capacitor-type cathode. In this study, we have synthesized a three-dimensional (3D) porous composite with uniformly incorporated MoS2 flocculent nanostructure onto 3D graphene via a facile solution-processed method as an anode for high-performance HSCs. This composite shows significantly enhanced electrochemical performance due to the synergistic effects of the conductive graphene sheets and the interconnected porous structure, which exhibits a high rate capability of 688 mAh/g even at a high current density of 8 A/g and a stable cycling performance (997 mAh/g after 700 cycles at 2 A/g). Furthermore, by using this composite as the anode for HSCs, the HSC shows a high energy density of 156 Wh/kg at 197 W/kg, which also remains at 97 Wh/kg even at a high power density of 8314 W/kg with a stable cycling life, among the best results of the reported HSCs thus far. PMID:26808826

  15. Photoactivation of the processes of formation of nanostructures by local anodic oxidation of a titanium film

    SciTech Connect

    Ageev, O. A.; Alyab'eva, N. I.; Konoplev, B. G. Polyakov, V. V.; Smirnov, V. A.

    2010-12-15

    Experimental results on the conditions of activation of probe nanolithography of a thin titanium film by means of local anodic oxidation are reported. It is established that ultraviolet stimulation reduces the geometric dimensions of nanometric oxide structures. The stimulation is accompanied by an increase in the amplitude and duration of the threshold voltage pulse, correspondingly, from 6 to 7 V and from 50 to 100 ms at the relative humidity 50%. The experimental data on the effect of the cantilever coating material and substrate temperature on the geometric dimensions of nanometric oxide structures are reported.

  16. Solution processed nickel oxide anodes for organic photovoltaic devices

    SciTech Connect

    Mustafa, Bestoon; Griffin, Jonathan; Alsulami, Abdullah S.; Lidzey, David G.; Buckley, Alastair R.

    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.

  17. Electric field control of magnetization in Cu2O/porous anodic alumina hybrid structures at room temperature

    NASA Astrophysics Data System (ADS)

    Qi, L. Q.; Liu, H. Y.; Sun, H. Y.; Liu, L. H.; Han, R. S.

    2016-04-01

    Cu2O nanoporous films are deposited on porous anodic alumina (PAA) substrates by DC-reactive magnetron sputtering. This paper focuses on voltage driven magnetization switching in Cu2O/PAA (CP) composite films prepared by DC-reactive magnetron sputtering. By applying a dc electric field, the magnetization of the CP composite films can be controlled in a reversible and reproducible way and shows an analogous on-off behavior. The magnitude of the change in the magnetization was about 75 emu/cm3 as the electric field was switched on and off. Resistive switching behavior was also observed in as-prepared CP composite films. Further analysis indicated that the formation/rupture of conducting filaments composed of oxygen vacancies is likely responsible for the changes in the magnetization as well as in the resistivity. Such reversible change of magnetization controlled by an electric field at room temperature may have applications in spintronics and power efficient data storage technologies.

  18. Si nanopatterning by reactive ion etching through an on-chip self-assembled porous anodic alumina mask

    PubMed Central

    2013-01-01

    Abstract We report on Si nanopatterning through an on-chip self-assembled porous anodic alumina (PAA) masking layer using reactive ion etching based on fluorine chemistry. Three different gases/gas mixtures were investigated: pure SF6, SF6/O2, and SF6/CHF3. For the first time, a systematic investigation of the etch rate and process anisotropy was performed. It was found that in all cases, the etch rate through the PAA mask was 2 to 3 times lower than that on non-masked areas. With SF6, the etching process is, as expected, isotropic. By the addition of O2, the etch rate does not significantly change, while anisotropy is slightly improved. The lowest etch rate and the best anisotropy were obtained with the SF6/CHF3 gas mixture. The pattern of the hexagonally arranged pores of the alumina film is, in this case, perfectly transferred to the Si surface. This is possible both on large areas and on restricted pre-defined areas on the Si wafer. PACS 78.67.Rb, 81.07.-b, 61.46.-w PMID:23402551

  19. A NiFeCu alloy anode catalyst for direct-methane solid oxide fuel cells

    NASA Astrophysics Data System (ADS)

    Wang, Wei; Zhu, Huaiyu; Yang, Guangming; Park, Hee Jung; Jung, Doh Won; Kwak, Chan; Shao, Zongping

    2014-07-01

    In this study, a new anode catalyst based on a NiFeCu alloy is investigated for use in direct-methane solid oxide fuel cells (SOFCs). The influence of the conductive copper introduced into the anode catalyst layer on the performance of the SOFCs is systematically studied. The catalytic activity for partial oxidation of methane and coking resistance tests are proposed with various anode catalyst layer materials prepared using different methods, including glycine nitrate process (GNP), physical mixing (PM) and impregnation (IMP). The surface conductivity tests indicate that the conductivities of the NiFe-ZrO2/Cu (PM) and NiFe-ZrO2/Cu (IMP) catalysts are considerably greater than that of NiFe-ZrO2/Cu (GNP), which is consistent with the SEM results. Among the three preparation methods, the cell containing the NiFe-ZrO2/Cu (IMP) catalyst layer performs best on CH4-O2 fuel, especially under reduced temperatures, because the coking resistance should be considered in real fuel cell conditions. The cell containing the NiFe-ZrO2/Cu (IMP) catalyst layer also delivers an excellent operational stability using CH4-O2 fuel for 100 h without any signs of decay. In summary, this work provides new alternative anode catalytic materials to accelerate the commercialization of SOFC technology.

  20. Anodic Oxidative Modification of Egg White for Heat Treatment.

    PubMed

    Takahashi, Masahito; Handa, Akihiro; Yamaguchi, Yusuke; Kodama, Risa; Chiba, Kazuhiro

    2016-08-31

    A new functionalization of egg white was achieved by an electrochemical reaction. The method involves electron transfer from thiol groups of egg white protein to form disulfide bonds. The oxidized egg white produced less hydrogen sulfide during heat treatment; with sufficient application of electricity, almost no hydrogen sulfide was produced. In addition, gels formed by heating electrochemically oxidized egg white exhibited unique properties, such as a lower gelation temperature and a softened texture, presumably due to protein aggregation and electrochemically mediated intramolecular disulfide bond formation. PMID:27518910

  1. Passivation and anodic oxidation of duplex TiN coating on stainless steel

    SciTech Connect

    Rudenja, S.; Pan, J.; Wallinder, I.O.; Leygraf, C.; Kulu, P.

    1999-11-01

    The passivation and anodic oxidation of duplex TiN coatings deposited by arc ion plating onto prenitrided AISI 304 stainless steel have been studied by potentiodynamic polarization, electrochemical impedance spectroscopy, and Mott-Schottky measurements in 0.1 M H{sub 2}SO{sub 4} + 0.05 M HCl. The chemical composition of the oxidized surface film atop TiN was analyzed by X-ray photoelectron spectroscopy. Up to 1.2 V/SHE the TiN coating exhibits passive behavior, which is attributed to the formation of a TiO{sub 2}-like film of nanometer thickness which grows linearly with anodic potential at a rate of 2.4 nm/V. Above 1.2 V/SHE enhanced anodic oxidation of TiN is observed at a rate of 17.7 nm/V, and the overall corrosion performance is governed both by the oxidized TiN coating and by a metallic Ti interlayer atop the nitrided stainless steel substrate. At all potentials the TiO{sub 2} film is characterized by relatively high donor densities and is, furthermore, terminated by a hydroxylated surface.

  2. Treatment of methyl orange dye wastewater by cooperative electrochemical oxidation in anodic-cathodic compartment.

    PubMed

    Pang, L; Wang, H; Bian, Z Y

    2013-01-01

    Electrochemical oxidation of methyl orange wastewater was studied using Ti/IrO(2)/RuO(2) anode and a self-made Pd/C O(2)-fed cathode in the divided cell with a terylene diaphragm. The result indicated that the appropriate rate of feeding air improved the methyl orange removal efficiency. The discoloration efficiency of methyl orange in the divided cell increased with increasing current density. The initial pH value had some effect on the discoloration of methyl orange, which became not obvious when the pH ranged from 2 to 10. However, the average removal efficiency of methyl orange wastewater in terms of total organic carbon (TOC) can reach 89.3%. The methyl orange structure had changed in the electrolytic process, and the characteristic absorption peak of methyl orange was about 470 nm. With the extension of electrolysis time, the concentration of methyl orange gradually reduced; wastewater discoloration rate increased gradually. The degradation of methyl orange was assumed to be cooperative oxidation by direct or indirect electrochemical oxidation at the anode and H(2)O(2), ·OH, O(2)(-)· produced by oxygen reduction at the cathode in the divided cell. Therefore, the cooperative electrochemical oxidation of methyl orange wastewater in the anodic-cathodic compartment had better degradation effects. PMID:23202555

  3. Composite solid oxide fuel cell anode based on ceria and strontium titanate

    DOEpatents

    Marina, Olga A.; Pederson, Larry R.

    2008-12-23

    An anode and method of making the same wherein the anode consists of two separate phases, one consisting of a doped strontium titanate phase and one consisting of a doped cerium oxide phase. The strontium titanate phase consists of Sr.sub.1-xM.sub.xTiO.sub.3-.delta., where M is either yttrium (Y), scandium (Sc), or lanthanum (La), where "x" may vary typically from about 0.01 to about 0.5, and where .delta. is indicative of some degree of oxygen non-stoichiometry. A small quantity of cerium may also substitute for titanium in the strontium titanate lattice. The cerium oxide consists of N.sub.yCe.sub.1-yO.sub.2-.delta., where N is either niobium (Nb), vanadium (V), antimony (Sb) or tantalum (Ta) and where "y" may vary typically from about 0.001 to about 0.1 and wherein the ratio of Ti in said first phase to the sum of Ce and N in the second phase is between about 0.2 to about 0.75. Small quantities of strontium, yttrium, and/or lanthanum may additionally substitute into the cerium oxide lattice. The combination of these two phases results in better performance than either phase used separately as an anode for solid oxide fuel cell or other electrochemical device.

  4. The contribution of mediated oxidation mechanisms in the electrolytic degradation of cyanuric acid using diamond anodes.

    PubMed

    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

  5. Fabrication and applications of nanocomposite structures using anodized aluminum oxide membranes

    NASA Astrophysics Data System (ADS)

    Gapin, Andrew Isaac

    As the field of nanotechnology continues to advance and device feature sizes scale down to ever smaller dimensions, it is becoming increasingly important to develop quick and efficient methods for large-scale production at the nanoscale. Creating such a template would have widespread uses in areas such as magnetic data storage, chemical sensors, and mask technology. One promising approach to realizing this goal may lie in utilizing the self-ordering behavior found in porous anodized aluminum oxide (AAO). This material offers many advantages such as the ability to customize the pore diameter and spacing and easy device integration based on its compatibility with silicon substrates. The pores of the AAO templates can be filled with many different materials via electrochemical deposition or other methods to produce numerous potential devices. In this work, current research results detailing the fabrication of AAO templates and their use in creating ˜100 nm tall CoPt, Ni, and composite Ni/CoPt nanowires is demonstrated. The synthesis of such nanostructures may ultimately be advantageous for new types of patterned magnetic recording media. The Ni nanowires exhibit relatively soft magnetic coercivity of 242 Oe, while the CoPt nanowires show a very high coercivity of at least 10.97 kOe, measured in the perpendicular direction along the nanowires axis. The composite soft magnet/hard magnet Ni/CoPt nanowires exhibit intermediate perpendicular coercivities depending on the relative amounts of Ni and CoPt. The Ni 80nm/CoPt20nm nanowires showed a coercivity of 1.96 kOe, the Ni50nm/CoPt50nm nanowires had a coercivity of 3.59 kOe, and the Ni20nm/CoPt80nm nanowires had a coercivity of 5.10 kOe. This marked decrease in the coercivity is significant because it could facilitate easier magnetic data writing. Analysis of the magnetic properties of the various nanowire structures and their dependence on the processing parameters is presented. A method for utilizing the AAO structure

  6. Facile Synthesis of Mn-Doped ZnO Porous Nanosheets as Anode Materials for Lithium Ion Batteries with a Better Cycle Durability

    NASA Astrophysics Data System (ADS)

    Wang, Linlin; Tang, Kaibin; Zhang, Min; Xu, Jingli

    2015-07-01

    Porous Zn1 - x Mn x O ( x = 0.1, 0.2, 0.44) nanosheets were prepared by a low-cost, large-scale production and simple approach, and the applications of these nanosheets as an anode material for Li-ion batteries (LIBs) were explored. Electrochemical measurements showed that the porous Zn0.8Mn0.2O nanosheets still delivered a stable reversible capacity of 210 mA h g-1 at a current rate of 120 mA g-1 up to 300 cycles. These results suggest that the facile synthetic method of producing porous Zn0.8Mn0.2O nanostructure can realize a better cycle durability with stable reversible capacity.

  7. Facile Synthesis of Mn-Doped ZnO Porous Nanosheets as Anode Materials for Lithium Ion Batteries with a Better Cycle Durability.

    PubMed

    Wang, Linlin; Tang, Kaibin; Zhang, Min; Xu, Jingli

    2015-12-01

    Porous Zn1 - x Mn x O (x = 0.1, 0.2, 0.44) nanosheets were prepared by a low-cost, large-scale production and simple approach, and the applications of these nanosheets as an anode material for Li-ion batteries (LIBs) were explored. Electrochemical measurements showed that the porous Zn0.8Mn0.2O nanosheets still delivered a stable reversible capacity of 210 mA h g(-1) at a current rate of 120 mA g(-1) up to 300 cycles. These results suggest that the facile synthetic method of producing porous Zn0.8Mn0.2O nanostructure can realize a better cycle durability with stable reversible capacity. PMID:26138451

  8. Increasing the Thermal Stability of Aluminum Titanate for Solid Oxide Fuel Cell Anodes

    NASA Technical Reports Server (NTRS)

    Bender, Jeffrey B.

    2004-01-01

    Solid-oxide fuel cells (SOFCs) show great potential as a power source for future space exploration missions. Because SOFCs operate at temperatures significantly higher than other types of fuel cells, they can reach overall efficiencies of up to 60% and are able to utilize fossil fuels. The SOFC team at GRC is leading NASA's effort to develop a solid oxide fuel cell with a power density high enough to be used for aeronautics and space applications, which is approximately ten times higher than ground transport targets. layers must be able to operate as a single unit at temperatures upwards of 900'C for at least 40,000 hours with less than ten percent degradation. One key challenge to meeting this goal arises from the thermal expansion mismatch between different layers. The amount a material expands upon heating is expressed by its coefficient of thermal expansion (CTE). If the CTEs of adjacent layers are substantially different, thermal stresses will arise during the cell's fabrication and operation. These stresses, accompanied by thermal cycling, can fracture and destroy the cell. While this is not an issue at the electrolyte-cathode interface, it is a major concern at the electrolyte-anode interface, especially in high power anode-supported systems. electrolyte are nearly identical. Conventionally, this has been accomplished by varying the composition of the anode to match the CTE of the yittria-stabilized zirconia (YSZ) electrolyte (approx.10.8x10(exp -6/degC). A Ni/YSZ composite is typically used as a base material for the anode due to its excellent electrochemical properties, but its CTE is about 13.4x10(exp -6/degC). One potential way to lower the CTE of this anode is to add a small percentage of polycrystalline Al2TiO5, with a CTE of 0.68x10(exp -6/degC, to the Ni/YSZ base. However, Al2TiO5 is thermally unstable and loses its effectiveness as it decomposes to Al2O3 and TiO2 between 750 C and 1280 C. be used as additives to increase the thermal stability of Al2

  9. Improving dielectric performance in anodic aluminum oxide via detection and passivation of defect states

    SciTech Connect

    Mibus, M.; Zangari, G.; Jensen, C.; Hu, X.; Reed, M. L.; Knospe, C.

    2014-06-16

    The electronic and ionic transports in 32–56 nm thick anodic aluminum oxide films are investigated before and after a 1-h anneal at 200–400 °C in argon. Results are correlated to their defect density as measured by the Mott-Schottky technique. Solid state measurements show that electronic conduction upon annealing is hindered by an increase in the Schottky emission barrier, induced by a reduction in dopant density. Using an electrochemical contact, the films fail rapidly under cathodic polarization, unless defect density is decreased down to 10{sup 17} cm{sup −3}, resulting in a three order of magnitude reduction in current and no visible gas evolution. Under anodic polarization, the decrease in defect density delays the onset of ionic conduction as well as further oxide growth and failure.

  10. NANOSTRUCTURED METAL OXIDES FOR ANODES OF LI-ION RECHARGEABLE BATTERIES

    SciTech Connect

    Au, M.

    2009-12-04

    The aligned nanorods of Co{sub 3}O{sub 4} and nanoporous hollow spheres (NHS) of SnO{sub 2} and Mn{sub 2}O{sub 3} were investigated as the anodes for Li-ion rechargeable batteries. The Co{sub 3}O{sub 4} nanorods demonstrated 1433 mAh/g reversible capacity. The NHS of SnO{sub 2} and Mn{sub 2}O{sub 3} delivered 400 mAh/g and 250 mAh/g capacities respectively in multiple galvonastatic discharge-charge cycles. It was found that high capacity of NHS of metal oxides is sustainable attributed to their unique structure that maintains material integrity during cycling. The nanostructured metal oxides exhibit great potential as the new anode materials for Li-ion rechargeable batteries with high energy density, low cost and inherent safety.

  11. Assessment of perovskite-type La0.8Sr0.2ScxMn1-xO3-δ oxides as anodes for intermediate-temperature solid oxide fuel cells using hydrocarbon fuels

    NASA Astrophysics Data System (ADS)

    Sengodan, S.; Yeo, H. J.; Shin, J. Y.; Kim, G.

    2011-03-01

    Composites formed by the infiltration of 40 wt% La0.8Sr0.2ScxMn1-xO3-δ (LSSM) oxides (x = 0.1, 0.2, 0.3) into 65% porous yttria-stabilized zirconia (YSZ) are investigated as anode materials for intermediate-temperature solid oxide fuel cells for hydrocarbon oxidation. The oxygen non-stoichiometry and electrical conductivity of each LSSM-YSZ composite are determined by coulometric titration. As the concentration of Sc increases, the composites show higher phase stability and the electrical conductivity of LSSM is significantly affected by the Sc doping, the non-stoichiometric oxygen content, and oxygen partial pressure (p(O2)). To achieve better electrochemical performance, it is necessary to add ceria-supported palladium catalyst for operation with humidified CH4. Anode polarization resistance increases with Sc doping due to a decrease in electrical conductivity. An electrolyte-supported cell with a LSSM-YSZ composite anode delivers peak power densities of 395 and 340 mW cm-2 at 923 K in humidified (3% H2O) H2 and CH4, respectively, at a flow rate of 20 mL min-1.

  12. Polymer Photovoltaic Cells with Rhenium Oxide as Anode Interlayer

    PubMed Central

    Wei, Jinyu; Bai, Dongdong; Yang, Liying

    2015-01-01

    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. PMID:26226439

  13. Polymer Photovoltaic Cells with Rhenium Oxide as Anode Interlayer.

    PubMed

    Wei, Jinyu; Bai, Dongdong; Yang, Liying

    2015-01-01

    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. PMID:26226439

  14. A facile synthesis of zinc oxide/multiwalled carbon nanotube nanocomposite lithium ion battery anodes by sol-gel method

    NASA Astrophysics Data System (ADS)

    Köse, Hilal; Karaal, Şeyma; Aydın, Ali Osman; Akbulut, Hatem

    2015-11-01

    Free standing zinc oxide (ZnO) and multiwalled carbon nanotube (MWCNT) nanocomposite materials are prepared by a sol gel technique giving a new high capacity anode material for lithium ion batteries. Free-standing ZnO/MWCNT nanocomposite anodes with two different chelating agent additives, triethanolamine (TEA) and glycerin (GLY), yield different electrochemical performances. Field emission gun scanning electron microscopy (FEG-SEM), energy dispersive X-ray spectrometer (EDS), high resolution transmission electron microscopy (HRTEM) and X-ray diffraction (XRD) analyses reveal the produced anode electrodes exhibit a unique structure of ZnO coating on the MWCNT surfaces. Li-ion cell assembly using a ZnO/MWCNT/GLY free-standing anode and Li metal cathode possesses the best discharge capacity, remaining as high as 460 mAh g-1 after 100 cycles. This core-shell structured anode can offer increased energy storage and performance over conventional anodes in Li-ion batteries.

  15. Graphite coated with manganese oxide/multiwall carbon nanotubes composites as anodes in marine benthic microbial fuel cells

    NASA Astrophysics Data System (ADS)

    Fu, Yubin; Yu, Jian; Zhang, Yelong; Meng, Yao

    2014-10-01

    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 (MnO2)/multiwall carbon nanotubes (MWCNTs) composites are prepared to be as novel anodes in the BMFCs via a direct redox reaction between permanganate ions (MnO4-) and MWCNTs. The results indicate that the MnO2/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 MnO2 (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. Nanoparticle Decorated Ultrathin Porous Nanosheets as Hierarchical Co3O4 Nanostructures for Lithium Ion Battery Anode Materials.

    PubMed

    Mujtaba, Jawayria; Sun, Hongyu; Huang, Guoyong; Mølhave, Kristian; Liu, Yanguo; Zhao, Yanyan; Wang, Xun; Xu, Shengming; Zhu, Jing

    2016-01-01

    We report a facile synthesis of a novel cobalt oxide (Co3O4) hierarchical nanostructure, in which crystalline core-amorphous shell Co3O4 nanoparticles with a bimodal size distribution are uniformly dispersed on ultrathin Co3O4 nanosheets. When tested as anode materials for lithium ion batteries, the as-prepared Co3O4 hierarchical electrodes delivered high lithium storage properties comparing to the other Co3O4 nanostructures, including a high reversible capacity of 1053.1 mAhg(-1) after 50 cycles at a current density of 0.2 C (1 C = 890 mAg(-1)), good cycling stability and rate capability. PMID:26846434

  17. Nanoparticle Decorated Ultrathin Porous Nanosheets as Hierarchical Co3O4 Nanostructures for Lithium Ion Battery Anode Materials

    PubMed Central

    Mujtaba, Jawayria; Sun, Hongyu; Huang, Guoyong; Mølhave, Kristian; Liu, Yanguo; Zhao, Yanyan; Wang, Xun; Xu, Shengming; Zhu, Jing

    2016-01-01

    We report a facile synthesis of a novel cobalt oxide (Co3O4) hierarchical nanostructure, in which crystalline core-amorphous shell Co3O4 nanoparticles with a bimodal size distribution are uniformly dispersed on ultrathin Co3O4 nanosheets. When tested as anode materials for lithium ion batteries, the as-prepared Co3O4 hierarchical electrodes delivered high lithium storage properties comparing to the other Co3O4 nanostructures, including a high reversible capacity of 1053.1 mAhg−1 after 50 cycles at a current density of 0.2 C (1 C = 890 mAg−1), good cycling stability and rate capability. PMID:26846434

  18. Nanoparticle Decorated Ultrathin Porous Nanosheets as Hierarchical Co3O4 Nanostructures for Lithium Ion Battery Anode Materials

    NASA Astrophysics Data System (ADS)

    Mujtaba, Jawayria; Sun, Hongyu; Huang, Guoyong; Mølhave, Kristian; Liu, Yanguo; Zhao, Yanyan; Wang, Xun; Xu, Shengming; Zhu, Jing

    2016-02-01

    We report a facile synthesis of a novel cobalt oxide (Co3O4) hierarchical nanostructure, in which crystalline core-amorphous shell Co3O4 nanoparticles with a bimodal size distribution are uniformly dispersed on ultrathin Co3O4 nanosheets. When tested as anode materials for lithium ion batteries, the as-prepared Co3O4 hierarchical electrodes delivered high lithium storage properties comparing to the other Co3O4 nanostructures, including a high reversible capacity of 1053.1 mAhg-1 after 50 cycles at a current density of 0.2 C (1 C = 890 mAg-1), good cycling stability and rate capability.

  19. Porous Pt Nanotubes with High Methanol Oxidation Electrocatalytic Activity Based on Original Bamboo-Shaped Te Nanotubes.

    PubMed

    Lou, Yue; Li, Chunguang; Gao, Xuedong; Bai, Tianyu; Chen, Cailing; Huang, He; Liang, Chen; Shi, Zhan; Feng, Shouhua

    2016-06-29

    In this report, a facile and general strategy was developed to synthesize original bamboo-shaped Te nanotubes (NTs) with well-controlled size and morphology. On the basis of the as-prepared Te NTs, porous Pt nanotubes (NTs) with excellent property and structural stability have been designed and manufactured. Importantly, we avoided the use of surface stabilizing agents, which may affect the catalytic properties during the templated synthesis process. Furthermore, Pt NTs with different morphology were successfully prepared by tuning the experimental parameters. As a result, transmission electron microscopy (TEM) study shows that both Te NTs and Pt NTs have uniform size and morphology. Following cyclic voltammogram (CV) testing, the as-prepared porous Pt NTs and macroporous Pt NTs exhibited excellent catalytic activities toward electrochemical methanol oxidation reactions due to their tubiform structure with nanoporous framework. Thus, the as-prepared Pt NTs with specific porous structure hold potential usage as alternative anode catalysts for direct methanol fuel cells (DMFCs). PMID:27310183

  20. Transformation and removal of arsenic in groundwater by sequential anodic oxidation and electrocoagulation

    NASA Astrophysics Data System (ADS)

    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.

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

    PubMed

    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. PMID:24689687

  2. Improved biological performance of low modulus Ti-24Nb-4Zr-7.9Sn implants due to surface modification by anodic oxidation

    NASA Astrophysics Data System (ADS)

    Gao, Y.; Gao, B.; Wang, R.; Wu, J.; Zhang, L. J.; Hao, Y. L.; Tao, X. J.

    2009-02-01

    Dental implants are usually made from commercially pure titanium or titanium alloys. The purpose of this study was to evaluate the influence of surface treatment to low modulus Ti-24Nb-4Zr-7.9Sn (TNZS) on cell and bone responses. The TNZS alloy samples were modified using anodic oxidation (AD). Surface oxide properties were characterized by using various surface analytic techniques, involving scanning electron microscopy (SEM) equipped with energy dispersive spectrometer (EDS), X-ray diffractometry (XRD) and surface profilometer. During the AD treatment, porous titanium oxide layer was formed and Ca ions were incorporated into the oxide layer. The viability and morphology of osteoblasts on Ca-incorporated TNZS were studied. The bone responses of Ca-incorporated TNZS were evaluated by pull-out tests and morphological analysis after implantation in rabbit tibiae. The non-treated Ti and TNZS samples were used as the control. Significant increases in cell viability and pull-out forces ( p < 0.05) were observed for Ca-incorporated TNZS implants compared with those for the control groups. Porous structures supplied positive guidance cues for osteoblasts to attach. The enhanced cell and bone responses to Ca-incorporated TNZS implants could be explained by the surface chemistry and microtopography.

  3. Novel enhancement of thin-form-factor galvanic cells: Probing halogenated organic oxidizers and metal anodes

    NASA Astrophysics Data System (ADS)

    Cardenas-Valencia, Andres M.; Adornato, Lori; Short, R. Timothy; Langebrake, Larry

    The work reported herein demonstrates a novel method to improve the overall performance of thin-form-factor galvanic cells, fabricated via micro-electromechanical systems (MEMS) processes. Use of solid, low cost, cyclic-halogenated, organic catholyte materials permits water activation of cells consisting of metal anode and catalytic platinum positive electrodes. Similar cells, employing aluminum and zinc anodes, have been activated using sodium hypochlorite (NaClO) solutions, i.e. bleach, in the past. The oxidizers chosen for this study (bromo-, chloro- and iodo-succinimides, and sodium dichloroisocyanuric acid) supply the cathode's oxy-halogenated ions when in contact with water. Zinc, magnesium and aluminum anodes are utilized to fabricate galvanic cells. A comparison between these anodes, coupled with various oxidizers, is included herein. Results using aluminum anode cells show that, even though the utilization efficiency of the catholyte reagents is low (faradic efficiencies between 16 and 19%), the performance of the new water-activated cells (6 cm × 6 cm × 0.25 cm) is superior when compared to those activated with bleach. For instance, operational lives of 6 h (activation with 10% NaClO solution) increase to more than 30 h using the new approach, with a 100-ohm-load. It is also shown that specific energies of 90-110 Wh kg -1 (calculated to include both reagent and packaging mass) could be obtained using the described approach with current draws between 10 and 20 mA. The specific energies obtained suggest that novel MEMS-type cells could have much broader application than low-current, bleach-activated cells.

  4. Retarding of electrochemical oxidation of formate on the platinum anode by a coat of Nafion membrane

    NASA Astrophysics Data System (ADS)

    Zhang, Rui; Lv, Weixin; Li, Guanghua; Mezaal, Mohammed Adnan; Li, Xiaojing; Lei, Lixu

    2014-12-01

    It has been found that the faradaic efficiency is decreasing with the electrolysis time for electrochemical reduction of CO2 to formate on a Sn cathode with a Pt anode in an undivided electrolytic cell, because the oxidation of formed formate takes place on the Pt anode, which also limits seriously the highest concentration of formate in the system. Here, we report that a coat of Nafion membrane on the Pt anode can retard the oxidation of formate: even if the concentration of the formate in the electrolyte reaches to 0.12 mol L-1, the faradaic efficiency still maintains above 61.3%; in contrast, the oxidation reaction of the formate on the naked Pt electrode is very fast, when the concentration of the formate in the electrolyte reaches to 0.023 mol L-1, the faradaic efficiency decreases to 35.3%. This is very important because the separation of formic acid could not be economical when its concentration is not high enough, and it is also costly if the depleted solution allows too less of its concentration because the solution has to be reused in the electrochemical process.

  5. Characterization of calcium phosphate deposited on valve metal by anodic oxidation with polarity inversion.

    PubMed

    Okawa, Seigo; Homma, Kikuo; Kanatani, Mitsugu; Watanabe, Kouichi

    2009-07-01

    Electrochemical deposition of calcium phosphate (CAP) on valve metals such as Ta, Nb, and Zr, was performed by anodic oxidation with alternate polarity inversion at an applied 20 VDC. A saturated hydroxyapatite(HAP)-phosphoric acid solution (pH 3) was used as the electrolyte. FTIR, XRD, and XPS were employed to investigate the detailed characteristics of the deposition. HAP was precipitated on Ta; HAP including brushite and monetite on Nb; and HAP and monetite on Zr. The Ca/P atomic ratios were 1.3-1.5 by XPS, and HPO(4)(2- )bands were detected on Ta by FTIR. Therefore, the HAP precipitated on Ta was a Ca-deficient HAP. In addition, the XPS spectra of the specimens showed that phosphate ions were incorporated into the anodic oxide film. Deposits with nano-grain size were observed by AFM. The results confirmed that CAP with nano-grain size was deposited on valve metals by the anodic oxidation with polarity inversion. PMID:19721291

  6. Plasma-enhanced atomic layer deposition of nanoscale yttria-stabilized zirconia electrolyte for solid oxide fuel cells with porous substrate.

    PubMed

    Ji, Sanghoon; Cho, Gu Young; Yu, Wonjong; Su, Pei-Chen; Lee, Min Hwan; Cha, Suk Won

    2015-02-11

    Nanoscale yttria-stabilized zirconia (YSZ) electrolyte film was deposited by plasma-enhanced atomic layer deposition (PEALD) on a porous anodic aluminum oxide supporting substrate for solid oxide fuel cells. The minimum thickness of PEALD-YSZ electrolyte required for a consistently high open circuit voltage of 1.17 V at 500 °C is 70 nm, which is much thinner than the reported thickness of 180 nm using nonplasmatic ALD and is also the thinnest attainable value reported in the literatures on a porous supporting substrate. By further reducing the electrolyte thickness, the grain size reduction resulted in high surface grain boundary density at the cathode/electrolyte interface. PMID:25625537

  7. Local anodic oxidation patterning of Au deposited Si surfaces.

    PubMed

    Vijaykumar, T; Kulkarni, G U

    2009-09-01

    Nanopatterning of Si(100) surfaces deposited with Au films from physical and chemical methods, has been carried out using a AFM set up mounted with a conducting tip. At a tip bias of -12 V, the LAO patterns drawn on various Au/SiOx surfaces have been compared with those on bare Si. The height of the oxide patterns is several times higher in the case of Au covered Si surfaces compared to patterns on bare Si surface. The enhancement in LAO is related to the catalytic activity of Au nanoparticulates at SiOx interface. PMID:19928226

  8. Formation of self-organized Zircaloy-4 oxide nanotubes in organic viscous electrolyte via anodization

    PubMed Central

    2014-01-01

    This work reports the formation of self-organized Zircaloy-4 (Zr-4) oxide nanotubes in viscous organic ethylene glycol (EG) electrolyte containing a small amount of fluoride salt and deionized (DI) water via an electrochemical anodization. The structure, morphology, and composition of the Zr-4 oxide nanotubes were studied using X-ray diffraction (XRD), scanning electron microscope (SEM), transmission electron microscope (TEM), EDX, and XPS. SEM results showed that the length of the nanotubes is approximately 13 μm, and TEM results showed that the inner diameter of the Zr-4 oxide nanotubes is approximately 20 nm with average wall thickness of approximately 7 nm. XRD and selected area electron diffraction pattern (SAED) results confirmed that the as-anodized Zr-4 oxide nanotubes have cubic crystalline structure. Both cubic and monoclinic phases were found after annealing of Zr-4 oxide nanotubes. The tubular structure morphology of Zr-4 oxide nanotubes did not remain intact after annealing which is attributed to the elimination of F species from the annealed nanotubes. PMID:25328503

  9. Aluminum oxide as a dual-functional modifier of Ni-based anodes of solid oxide fuel cells for operation on simulated biogas

    NASA Astrophysics Data System (ADS)

    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.

  10. Olive mill wastewater treatment by anodic oxidation with parallel plate electrodes.

    PubMed

    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

  11. Study of the processes of carbonization and oxidation of porous silicon by Raman and IR spectroscopy

    SciTech Connect

    Vasin, A. V.; Okholin, P. N.; Verovsky, I. N.; Nazarov, A. N.; Lysenko, V. S.; Kholostov, K. I. Bondarenko, V. P.; Ishikawa, Y.

    2011-03-15

    Porous silicon layers were produced by electrochemical etching of single-crystal silicon wafers with the resistivity 10 {Omega} cm in the aqueous-alcohol solution of hydrofluoric acid. Raman spectroscopy and infrared absorption spectroscopy are used to study the processes of interaction of porous silicon with undiluted acetylene at low temperatures and the processes of oxidation of carbonized porous silicon by water vapors. It is established that, even at the temperature 550 Degree-Sign C, the silicon-carbon bonds are formed at the pore surface and the graphite-like carbon condensate emerges. It is shown that the carbon condensate inhibits oxidation of porous silicon by water vapors and contributes to quenching of white photoluminescence in the oxidized carbonized porous silicon nanocomposite layer.

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

    NASA Astrophysics Data System (ADS)

    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 < carbon dioxide/methane ratio < 2, which is an interesting result for prospective direct biogas fueled SOFCs. Conversion is stable over a period of 70 h. Both for temperatures lower than 450 °C and for carbon dioxide-methane ratios lower than equi-molar at 800 °C, conversion is poor due to low activity of the anode toward dry reforming and cracking 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.

  13. Nanosegregated bimetallic oxide anode catalyst for proton exchange membrane electrolyzer

    DOEpatents

    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.

  14. Degradation of anti-inflammatory drug ketoprofen by electro-oxidation: comparison of electro-Fenton and anodic oxidation processes.

    PubMed

    Feng, Ling; Oturan, Nihal; van Hullebusch, Eric D; Esposito, Giovanni; Oturan, Mehmet A

    2014-01-01

    The electrochemical degradation of the nonsteroidal anti-inflammatory drug ketoprofen in tap water has been studied using electro-Fenton (EF) and anodic oxidation (AO) processes with platinium (Pt) and boron-doped diamond (BDD) anodes and carbon felt cathode. Fast degradation of the parent drug molecule and its degradation intermediates leading to complete mineralization was achieved by BDD/carbon felt, Pt/carbon felt, and AO with BDD anode. The obtained results showed that oxidative degradation rate of ketoprofen and mineralization of its aqueous solution increased by increasing applied current. Degradation kinetics fitted well to a pseudo-first-order reaction. Absolute rate constant of the oxidation of ketoprofen by electrochemically generated hydroxyl radicals was determined to be (2.8 ± 0.1) × 10(9) M(-1) s(-1) by using competition kinetic method. Several reaction intermediates such as 3-hydroxybenzoic acid, pyrogallol, catechol, benzophenone, benzoic acid, and hydroquinone were identified by high-performance liquid chromatography (HPLC) analyses. The formation, identification, and evolution of short-chain aliphatic carboxylic acids like formic, acetic, oxalic, glycolic, and glyoxylic acids were monitored with ion exclusion chromatography. Based on the identified aromatic/cyclic intermediates and carboxylic acids as end products before mineralization, a plausible mineralization pathway was proposed. The evolution of the toxicity during treatments was also monitored using Microtox method, showing a faster detoxification with higher applied current values. PMID:24756667

  15. Influence of electropolishing and anodic oxidation on morphology, chemical composition and corrosion resistance of niobium.

    PubMed

    Sowa, Maciej; Greń, Katarzyna; Kukharenko, Andrey I; Korotin, Danila M; Michalska, Joanna; Szyk-Warszyńska, Lilianna; Mosiałek, Michał; Zak, Jerzy; Pamuła, Elżbieta; Kurmaev, Ernst Z; Cholakh, Seif O; Simka, Wojciech

    2014-09-01

    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 1moldm(-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. PMID:25063150

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

    SciTech Connect

    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.

  17. Angle selective light management in photovoltaics using self-assembled anodized aluminum oxide nanopatterns

    NASA Astrophysics Data System (ADS)

    Roberts, Brian; Ku, P.-C.

    2015-03-01

    Semitransparent photovoltaics are of interest for building integration and window coatings, though demonstrate an intrinsic tradeoff between transparency and absorption / efficiency. We propose alleviating this tradeoff using light management nanostructures which selectively scatter light based on incident wavelength and angle, allowing transmission of normally incident light for window visibility and absorption of light at elevated angles. Two structures of interest are proposed and described: metal nanorods which scatter light via their localized surface plasmon resonance properties, and arrays of subwavelength nanopores in a dielectric which demonstrate coherent multiple scattering. Both structures can potentially be patterned over large areas by electrochemical oxidation of aluminum into self assembled nanoporous anodized aluminum oxide (AAO) films.

  18. Porous Iron Cobaltate Nanoneedles Array on Nickel Foam as Anode Materials for Lithium-Ion Batteries with Enhanced Electrochemical Performance.

    PubMed

    Liu, Li; Zhang, Huijuan; Mu, Yanping; Yang, Jiao; Wang, Yu

    2016-01-20

    A monocrystalline and porous FeCo2O4 nanoneedles array growing directly on a nickel foam substrate was obtained by a hydrothermal technique accompanying with combustion of the one-dimensional precursor. The average length of the FeCo2O4 nanoneedles is approximately 2 μm, while the diameter of the root segment of the nanoneedle can be estimated to be around 100 nm, which gradually reduces to only several nanometers at the top. When the as-prepared porous FeCo2O4 nanoneedles array with a high surface area of 58.49 m(2) g(-1) was applied as binder-free electrode in lithium-ion batteries, it exhibited satisfactory electrochemical performance, such as outstanding reversibility (Coulombic efficiency of approximately 92-95%), high specific capacity (1962 mAh g(-1) at the current density of 100 mA g(-1)), and excellent rate performance (discharge capacity of 875 mAh g(-1) at the current density of 2000 mA g(-1)), due to the various favorable conditions. Undoubtedly, the simple but effective strategy can be expanded to other high-performance binary metal-oxide materials. PMID:26713359

  19. Post-annealing of thin-film yttria stabilized zirconia electrolytes for anode-supported low-temperature solid oxide fuel cells.

    PubMed

    Bae, Jiwoong; Chang, Ikwhang; Kang, Sungmin; Hong, Soonwook; Cha, Suk Won; Kim, Young Beom

    2014-12-01

    The effects of a post-annealing treatment on the performance of low-temperature solid oxide fuel cells (LT-SOFCs) were investigated. Nickel oxide-samarium doped ceria (NiO-SDC) anodes and yttria stabilized zirconia (YSZ) electrolytes were deposited on anodized aluminum oxide (AAO) membranes by RF sputtering and DC reactive sputtering, respectively. The half-cell of YSZ/NiO-SDC was then heat-treated at 600 degrees C for 10 h, and a porous platinum (Pt) cathode was deposited on the annealed YSZ/NiO-SDC structure by DC magnetron sputtering. Electrochemical impedance spectroscopy (EIS) analysis revealed a significant decrease in the ohmic resistance and a slight increase in the cathodic impedance. Such a result may be attributed to the increased grain size and enhanced crystallinity of the YSZ electrolyte after the heat treatment. The maximum power density observed for the heat-treated cell was 35 mW/cm2 at 450 degrees C, more than three times higher than the 10 mW/cm2 value obtained for the as-deposited cell. PMID:25971054

  20. Effects of Nanoporous Anodic Alumina Oxide on the Crystallization and Melting Behavior of Poly(vinylidene fluoride).

    PubMed

    Dai, Xiying; Niu, Jiali; Ren, Zhongjie; Sun, Xiaoli; Yan, Shouke

    2016-02-01

    Poly(vinylidene fluoride) (PVDF) nanotubes were fabricated by melt-wetting into porous anodic aluminum oxide (AAO) templates with two different interfacial properties: one is pristine AAO, and the other is modified by FOTS (AAO-F). Their crystallization and melting behaviors are compared with those of a bulk sample. For the PVDF in AAO-F, the nonisothermal crystallization temperature is slightly lower than that of bulk, and the melting temperature is similar to that of bulk. For the PVDF in pristine AAO, when the pore diameter is 200 nm, the crystallization is induced by two kinds of nucleation: heterogeneous nucleation and interface-induced nucleation. On the contrary, in the AAO template with pore diameter smaller than 200 nm, only interface-induced nucleation occurs. The melting temperature of PVDF crystals in the pristine AAO is much higher than that of bulk which can be attributed to the presence of an interfacial layer of PVDF on the template inner surface. The interaction between PVDF and AAO template produces the interfacial layer. Such an interfacial layer plays an important role in enhancing the melting temperature of PVDF crystals. The higher melting peak is always observed when the PVDF is nonisothermally crystallized in the AAO template irrespective of the thermal erasing temperature suggesting the interfacial layer is very stable on the AAO template surface. If the PVDF nanostructures are released from AAO template, the higher melting peak disappears with the enhancement of thermal erasing temperature. PMID:26745857

  1. Anodized Steel Electrodes for Supercapacitors.

    PubMed

    Sagu, Jagdeep S; Wijayantha, K G Upul; Bohm, Mallika; Bohm, Siva; Kumar Rout, Tapan

    2016-03-01

    Steel was anodized in 10 M NaOH to enhance its surface texture and internal surface area for application as an electrode in supercapacitors. A mechanism was proposed for the anodization process. Field-emission gun scanning electron microscopy (FEGSEM) studies of anodized steel revealed that it contains a highly porous sponge like structure ideal for supercapacitor electrodes. X-ray photoelectron spectroscopy (XPS) measurements showed that the surface of the anodized steel was Fe2O3, whereas X-ray diffraction (XRD) measurements indicated that the bulk remained as metallic Fe. The supercapacitor performance of the anodized steel was tested in 1 M NaOH and a capacitance of 18 mF cm(-2) was obtained. Cyclic voltammetry measurements showed that there was a large psueudocapacitive contribution which was due to oxidation of Fe to Fe(OH)2 and then further oxidation to FeOOH, and the respective reduction of these species back to metallic Fe. These redox processes were found to be remarkably reversible as the electrode showed no loss in capacitance after 10000 cycles. The results demonstrate that anodization of steel is a suitable method to produce high-surface-area electrodes for supercapacitors with excellent cycling lifetime. PMID:26891093

  2. A three-dimensional porous MoP@C hybrid as a high-capacity, long-cycle life anode material for lithium-ion batteries

    NASA Astrophysics Data System (ADS)

    Wang, Xia; Sun, Pingping; Qin, Jinwen; Wang, Jianqiang; Xiao, Ying; Cao, Minhua

    2016-05-01

    Metal phosphides are great promising anode materials for lithium-ion batteries with a high gravimetric capacity. However, significant challenges such as low capacity, fast capacity fading and poor cycle stability must be addressed for their practical applications. Herein, we demonstrate a versatile strategy for the synthesis of a novel three-dimensional porous molybdenum phosphide@carbon hybrid (3D porous MoP@C hybrid) by a template sol-gel method followed by an annealing treatment. The resultant hybrid exhibits a 3D interconnected ordered porous structure with a relatively high surface area. Benefiting from its advantages of microstructure and composition, the 3D porous MoP@C hybrid displays excellent lithium storage performance as an anode material for lithium-ion batteries in terms of specific capacity, cycling stability and long-cycle life. It presents stable cycling performance with a high reversible capacity up to 1028 mA h g-1 at a current density of 100 mA g-1 after 100 cycles. By ex situ XRD, HRTEM, SAED and XPS analyses, the 3D porous MoP@C hybrid was found to follow the Li-intercalation reaction mechanism (MoP + xLi+ + e- <--> LixMoP), which was further confirmed by ab initio calculations based on density functional theory.Metal phosphides are great promising anode materials for lithium-ion batteries with a high gravimetric capacity. However, significant challenges such as low capacity, fast capacity fading and poor cycle stability must be addressed for their practical applications. Herein, we demonstrate a versatile strategy for the synthesis of a novel three-dimensional porous molybdenum phosphide@carbon hybrid (3D porous MoP@C hybrid) by a template sol-gel method followed by an annealing treatment. The resultant hybrid exhibits a 3D interconnected ordered porous structure with a relatively high surface area. Benefiting from its advantages of microstructure and composition, the 3D porous MoP@C hybrid displays excellent lithium storage performance as an

  3. Formation of the Microstructure of TiO2 Film Through Anodic Oxidation of Titanium

    NASA Astrophysics Data System (ADS)

    Yokogawa, Y.; Yasuki, T.; Hirotomi, T.; Nakamura, A.; Kishida, I.

    2011-04-01

    Recent titanium oxide nanotube arrays have attracted attention for their applications. Titanium oxide nanotubes were prepared under potentiostat conditions (10 - 60 V) for various times (1 min - 3 hr). SEM observations revealed that the pore sizes of the nanotubes have a tendency to increase with an increase in the applied potential in the NH4F-glycerol-H2O electrolyte. Some corrosive pores were observed on the surface of titanium substrate at 40 V for 1 minute at 40°C. The pores covered the surface of the titanium substrate after 10 minutes, and some small pores were observed in the inner part of the pores, which should correspond to the combining of some small adjacent pores into a large one. The combining of the tubes were observed after 2 h and 3 h anodization times, and the nanotube arrays seem to be formed upward from the SEM side-views. The photocatalytic activity of the titanium oxide nanotubes was evaluated according to the JIS standard (JIS R 1703-2). The R factor of the titanium oxide nanotube arrays formed at 40 V and 40°C for a 3h the anodization time was 9.71 n mol/l·min, which was twice that of the titanium oxide thin film obtained by the rf-sputtering method.

  4. Investigation on the Oxidation and Reduction of Titanium in Molten Salt with the Soluble TiC Anode

    NASA Astrophysics Data System (ADS)

    Wang, Shulan; Wan, Chaopin; Liu, Xuan; Li, Li

    2015-12-01

    To reveal the oxidation process of titanium from TiC anode and the reduction mechanism of titanium ions in molten NaCl-KCl, the polarization curve of TiC anode in molten NaCl-KCl and cyclic voltammograms of the molten salt after polarization were studied. Investigation on the polarization curve shows that titanium can be oxidized and dissociated from the TiC anode at very low potential. The cyclic voltammograms demonstrated that the reduction reaction of titanium ions in the molten salt is a one-step process. By potentiostatic electrolysis, dendritic titanium is obtained on the steel plate. The work promotes the understanding on the process of electrochemical oxidization/dissociation of titanium from TiC anode and the reduction mechanism of titanium ions in molten salt.

  5. Adhesive strength of medical polymer on anodic oxide nanostructures fabricated on biomedical β-type titanium alloy.

    PubMed

    Hieda, Junko; Niinomi, Mitsuo; Nakai, Masaaki; Cho, Ken; Mohri, Tomoyoshi; Hanawa, Takao

    2014-03-01

    Anodic oxide nanostructures (nanopores and nanotubes) were fabricated on a biomedical β-type titanium alloy, Ti-29Nb-13Ta-4.6Zr alloy (TNTZ), by anodization in order to improve the adhesive strength of a medical polymer, segmented polyurethane (SPU), to TNTZ. TNTZ was anodized in 1.0M H3PO4 solution with 0.5 mass% NaF using a direct-current power supply at a voltage of 20V. A nanoporous structure is formed on TNTZ in the first stage of anodization, and the formation of a nanotube structure occurs subsequently beneath the nanoporous structure. The nanostructures formed on TNTZ by anodization for less than 3,600s exhibit higher adhesive strengths than those formed at longer anodization times. The adhesive strength of the SPU coating on the nanoporous structure formed on top of TNTZ by anodization for 1,200s improves by 144% compared to that of the SPU coating on as-polished TNTZ with a mirror surface. The adhesive strength of the SPU coating on the nanotube structure formed on TNTZ by anodization for 3,600s increases by 50%. These improvements in the adhesive strength of SPU are the result of an anchor effect introduced by the nanostructures formed by anodization. Fracture occurs at the interface of the nanoporous structure and the SPU coating layer. In contrast, in the case that SPU coating has been performed on the nanotube structure, fracture occurs inside the nanotubes. PMID:24433910

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

    NASA Astrophysics Data System (ADS)

    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.

  7. Improved electrochemical performance of yolk-shell structured SnO2@void@C porous nanowires as anode for lithium and sodium batteries

    NASA Astrophysics Data System (ADS)

    Li, H. Z.; Yang, L. Y.; Liu, J.; Li, S. T.; Fang, L. B.; Lu, Y. K.; Yang, H. R.; Liu, S. L.; Lei, M.

    2016-08-01

    Various yolk-shell structured particles designed for large volume expansion materials for lithium-ion storage have been reported, the cycle stability and coulombic efficiency can be effectively improved through such structure design. SnO2 has high theoretical capacity of 1494 mA h g-1 and 1378 mA h g-1 for lithium and sodium storage, respectively. The large volume expansion problem of SnO2 has long been considered as the primary reason for the capacity fading of SnO2 based anode materials. In this paper, the yolk-shell structured SnO2 porous nanowire has been designed, and this unique yolk-shell structure is reported as anode materials for lithium and sodium-ion storage for the first time. The yolk-shell structured porous nanowires deliver significantly improved cycle stability and coulombic efficiency as active material for both lithium and sodium-ion storage compared with that of pure SnO2 porous nanowires. It exhibits a high and stable capacity of 1150 mA h g-1 at current density of 200 mA g-1 for lithium-ion storage, and a capacity of 401 mA h g-1 at current density of 50 mA g-1 after 50 cycles for sodium-ion storage.

  8. Scalable Synthesis of Few-Layer MoS2 Incorporated into Hierarchical Porous Carbon Nanosheets for High-Performance Li- and Na-Ion Battery Anodes.

    PubMed

    Park, Seung-Keun; Lee, Jeongyeon; Bong, Sungyool; Jang, Byungchul; Seong, Kwang-Dong; Piao, Yuanzhe

    2016-08-01

    It is still a challenging task to develop a facile and scalable process to synthesize porous hybrid materials with high electrochemical performance. Herein, a scalable strategy is developed for the synthesis of few-layer MoS2 incorporated into hierarchical porous carbon (MHPC) nanosheet composites as anode materials for both Li- (LIB) and Na-ion battery (SIB). An inexpensive oleylamine (OA) is introduced to not only serve as a hinder the stacking of MoS2 nanosheets but also to provide a conductive carbon, allowing large scale production. In addition, a SiO2 template is adopted to direct the growth of both carbon and MoS2 nanosheets, resulting in the formation of hierarchical porous structures with interconnected networks. Due to these unique features, the as-obtained MHPC shows substantial reversible capacity and very long cycling performance when used as an anode material for LIBs and SIBs, even at high current density. Indeed, this material delivers reversible capacities of 732 and 280 mA h g(-1) after 300 cycles at 1 A g(-1) in LIBs and SIBs, respectively. The results suggest that these MHPC composites also have tremendous potential for applications in other fields. PMID:27406553

  9. Improved electrochemical performance of yolk-shell structured SnO2@void@C porous nanowires as anode for lithium and sodium batteries

    NASA Astrophysics Data System (ADS)

    Li, H. Z.; Yang, L. Y.; Liu, J.; Li, S. T.; Fang, L. B.; Lu, Y. K.; Yang, H. R.; Liu, S. L.; Lei, M.

    2016-08-01

    Various yolk-shell structured particles designed for large volume expansion materials for lithium-ion storage have been reported, the cycle stability and coulombic efficiency can be effectively improved through such structure design. SnO2 has high theoretical capacity of 1494 mA h g-1 and 1378 mA h g-1 for lithium and sodium storage, respectively. The large volume expansion problem of SnO2 has long been considered as the primary reason for the capacity fading of SnO2 based anode materials. In this paper, the yolk-shell structured SnO2 porous nanowire has been designed, and this unique yolk-shell structure is reported as anode materials for lithium and sodium-ion storage for the first time. The yolk-shell structured porous nanowires deliver significantly improved cycle stability and coulombic efficiency as active material for both lithium and sodium-ion storage compared with that of pure SnO2 porous nanowires. It exhibits a high and stable capacity of 1150 mA h g-1 at current density of 200 mA g-1 for lithium-ion storage, and a capacity of 401 mA h g-1 at current density of 50 mA g-1 after 50 cycles for sodium-ion storage.

  10. Rational design of metal oxide nanocomposite anodes for advanced lithium ion batteries

    NASA Astrophysics Data System (ADS)

    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.

  11. Microstructure and polarization characteristics of anode supported tubular solid oxide fuel cell with co-precipitated and mechanically mixed Ni-YSZ anodes

    NASA Astrophysics Data System (ADS)

    Shikazono, Naoki; Sakamoto, Yusuke; Yamaguchi, Yu; Kasagi, Nobuhide

    An anode support tubular solid oxide fuel cell (SOFC) is fabricated and the dependence of its polarization resistance on anode microstructural parameters is investigated by means of stereology and concept of contiguity (c-c) theory. Nickel yttria-stabilized zirconia (Ni-YSZ) anode supported cell with YSZ electrolyte, lanthanum-strontium-manganite (LSM)-YSZ composite cathode, and LSM cathode layers is fabricated by dip coating. Submicrometer resolution images of anode microstructure are successfully obtained by low voltage SEM-EDX and quantified by stereological analysis. Cell voltage measurements and impedance spectroscopy are performed at temperatures of 650 and 750 °C with hydrogen and nitrogen mixture gas as a fuel. A quantitative relationship between polarization resistance and microstructural parameters such as circularity, three-phase boundary length, contiguity, etc. is investigated using the concept of contiguity (c-c) theory. The effectiveness of correlating polarization resistance of anode supported tubular SOFC using stereology and c-c theory is evaluated.

  12. Surface Characterization and Osteoconductivity Evaluation of Micro/Nano Surface Formed on Titanium Using Anodic Oxidation Combined with H2O2 Etching and Hydrothermal Treatment.

    PubMed

    Park, Eun-Jin; Song, Yo-Han; Hwang, Moon-Jin; Song, Ho-Jun; Park, Yeong-Joon

    2015-08-01

    In this study, surface characteristics and osteoconductivity were investigated for the micro/nanostructured oxide layers fabricated on titanium using anodic oxidation (ANO), chemical etching (Et), and hydrothermal treatment (HT). Commercially pure titanium (CP-Ti) disks were anodic-oxidized using DC-type power supply in 1 M phosphoric acid electrolyte (P-ANO group). These specimens were further chemically etched using 30% H2O2 solution at 60 °C for 10 min (P-ANO-Et group). The P-ANO-Et-HT group was fabricated by hydrothermally treating the P-ANO-Et specimens in phosphorus-containing alkaline solution at 190 °C for 8 hrs. The P-ANO group showed a porous surface that was evenly covered with micro- and sub-micro pores. The size of these pores was decreased in the P-ANO-Et group. The P-ANO-Et-HT group showed a porous surface that was covered with nano-sized crystallites. Anatase TiO2 structure was observed in P-ANO-Et-HT group. The results of XPS demonstrated that the P-ANO-Et-HT group had a well-crystallized TiC2 structure, while the P-ANO and P-ANO-Et groups had an amorphous and phosphate-containing structure. Hydrophilicity of the P-ANO-Et-HT group was the highest. After MG63 osteoblast-like cells were cultured on the specimens for 3 hrs, SEM images of the cells cultured on P-ANO-Et-HT group specimens showed low initial adhesion. However, the osteoconductivity of these specimens increased more rapidly compared to that of the micro-structured surfaces. These results could be applied to fabricate titanium implants with an optimum micro/nano-surface for enhancing their osteoconductivity. PMID:26369213

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

    NASA Astrophysics Data System (ADS)

    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.

  14. Fabrication of Chemically Tunable, Hierarchically Branched Polymeric Nanostructures by Multi-branched Anodic Aluminum Oxide Templates.

    PubMed

    Jo, Hanju; Haberkorn, Niko; Pan, Jia-Ahn; Vakili, Mohammad; Nielsch, Kornelius; Theato, Patrick

    2016-06-28

    In this paper, a template-assisted replication method is demonstrated for the fabrication of hierarchically branched polymeric nanostructures composed of post-modifiable poly(pentafluorophenyl acrylate). Anodic aluminum oxide templates with various shapes of hierarchically branched pores are fabricated by an asymmetric two-step anodization process. The hierarchical polymeric nanostructures are obtained by infiltration of pentafluorophenyl acrylate with a cross-linker and photoinitiator, followed by polymerization and selective removal of the template. Furthermore, the nanostructures containing reactive pentafluorophenyl ester are modified with spiropyran amine via post-polymerization modification to fabricate ultraviolet-responsive nanostructures. This method can be readily extended to other amines and offers a generalized strategy for controlling functionality and wettability of surfaces. PMID:27243550

  15. Influences of the main anodic electroplating parameters on cerium oxide films

    NASA Astrophysics Data System (ADS)

    Yang, Yang; Yang, Yumeng; Du, Xiaoqing; Chen, Yu; Zhang, Zhao; Zhang, Jianqing

    2014-06-01

    Cerium oxide thin films were fabricated onto 316 L stainless steel via a potentiostatically anodic electrodeposition approach in the solutions containing cerium(III) nitrate (0.05 M), ammonia acetate (0.1 M) and ethanol (10% V/V). The electrochemical behaviors and deposition parameters (applied potential, bath temperature, dissolving O2 and bath pH) have been investigated. Results show that, the electrochemical oxidation of Ce3+ goes through one electrochemical step, which is under charge transfer control. The optimum applied potential for film deposition is 0.8 V. Bath temperature plays a significant effect on the deposition rate, composition (different colors of the film) and surface morphology of the deposits. Due to the hydrolysis of Ce3+, cerous hydroxide is facility to form when the bath temperature is higher than 60 °C. The electroplating bath pH is another key role for the anodic deposition of cerium oxide thin films, and the best bath pH is around 6.20. N2 or O2 purged into the bath will result in film porosities and O2 favors cerium oxide particles and film generation.

  16. Characterization and quantification of oxides generated by anodization on titanium for implantation purposes

    NASA Astrophysics Data System (ADS)

    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).

  17. Synthesis and characterization of porous Mo-W oxide nanostructures.

    PubMed

    Paraguay-Delgado, F; Verde, Y; Cizniega, E; Lumbreras, J A; Alonso-Nuñez, G

    2008-12-01

    The present study reports the synthesis method, microstructure characterization, and thermal stability of nanostructured porous mixed oxide (MoO3-WO3) at 550 and 900 degrees C of annealing. The material was synthesized using a hydrothermal method. The precursor was prepared by aqueous solution using ammonium heptamolibdate and ammonium metatungstate, with an atomic ratio of Mo/W = 1. The pH was adjusted to 5, and then the solution was transferred to a teflon-lined stainless steel autoclave and heated at 200 degrees C for 48 h. The resultant material was washed using deionized water. The specific surface area, morphology, composition, and microstructure before and after annealing were studied by N2 physisorption, scanning electron microscopy (SEM), analytical transmission electron microscopy (TEM), and X-Ray diffraction (XRD). The initial synthesized materials showed low crystallinity and high specific surface area around (141 m2/g). After thermal annealing the material showed higher crystallinity and diminished its specific surface area drastically. PMID:19205219

  18. Porous graphene oxide-chitosan aerogel for tetracycline removal

    NASA Astrophysics Data System (ADS)

    Zhao, Lianqin; Dong, Pingjiang; Xie, Jingru; Li, Jiayan; Wu, Lixiang; Yang, Sheng-Tao; Luo, Jianbin

    2014-03-01

    Nanotechnology has brought new approaches for the treatment of antibiotics, which are potent pollutants to water. In this study, we reported that a porous graphene oxide-chitosan aerogel (PGO-CS) could be used as a recyclable adsorbent for tetracycline removal. PGO-CS adsorbed tetracycline with a capacity of around 1.47 × 103 mg g-1, ranking it among the most effective adsorbents for tetracycline. The adsorption equilibrium was well fitted to the Temkin model with a b value of 2.83 × 10-3 kJ mol-1. The adsorption kinetics was described by the pseudo-first-order model, giving a k1 value of -2.37 × 10-3 (1 min-1). The intraparticle model fitting suggested that the adsorption involved intraparticle diffusion and surface diffusion. In the thermodynamics investigation, the negative ΔG implied that the adsorption was spontaneous and physisorption in nature. The positive ΔH demonstrated that the adsorption process was endothermic and the adsorption was mainly driven by the increased randomness. Higher pH and ionic strength facilitated the adsorption significantly. In addition, PGO-CS was easily regenerated by washing with HCl aqueous solution.

  19. Porous structured vanadium oxide electrode material for electrochemical capacitors

    NASA Astrophysics Data System (ADS)

    Reddy, Ravinder N.; Reddy, Ramana G.

    A nano porous vanadium oxide (V 2O 5) was prepared by sol-gel method. The preparation involved elutriation of aqueous sodium meta vanadate over a cation exchange resin. The product was characterized using X-ray diffraction, scanning electron microscopy, energy dispersive spectroscopy, surface area analysis and thermogravimetric analysis. Electrochemical characterization was done using cyclic voltammetry in a three electrode system consisting of a saturated calomel electrode as reference electrode, platinum mesh as a counter electrode, and V 2O 5 mounted on Ti mesh as the working electrode. Two molars of aqueous KCl, NaCl and LiCl were used as electrolytes. A maximum capacitance of 214 F g -1 was obtained at a scan rate of 5 mV s -1 in 2 M KCl. The effect of different electrolytes and the effect of concentration of KCl on the specific capacitance of V 2O 5 were studied. Specific capacitance faded rapidly over 100 cycles in 2 M KCl at a 5 mV s -1 scan rate.

  20. Comparative study of metal or oxide capped indium-tin oxide anodes for organic light-emitting diodes

    NASA Astrophysics Data System (ADS)

    Qiu, Chengfeng; Xie, Zhilang; Chen, Haiying; Wong, Man; Kwok, Hoi Sing

    2003-03-01

    Indium-tin oxide capped with a variety of nanometer-thick metal or oxide buffer layers has been investigated as anodes in organic light-emitting diodes based on N,N'-diphenyl-N,N' bis(3-methyl-phenyl-1,1'-biphenyl-4,4'-diamine/tris-8-hydroxyquinoline aluminum. Although high work-function metal buffer layers led to enhancement in hole-injection efficiency, none of the metals investigated gave rise to improvement in current or power efficiency. On the other hand, diodes with some of the oxide buffer layers exhibited improvement not only in hole injection but also in power efficiency. In particular, when 1 nm thick praseodymium oxide was used as the cap layer, more than double the power efficiency was obtained.

  1. Synthesis and photocatalytic property of porous metal oxides nanowires based on carbon nanofiber template

    NASA Astrophysics Data System (ADS)

    Fan, Weiqiang; Li, Meng; Xu, Jinfu; Bai, Hongye; Zhang, Rongxian; Chen, Chao

    2015-11-01

    A series of porous metal oxides nanowires (Fe2O3, Co3O4, NiO and CuO) have been successfully synthesized, where commercial carbon nanofibers were used as the template. The obtained samples were systematically characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), UV-Vis diffuse reflectance (UV-Vis DR) spectra and transmission electron microscope (TEM). According to the photodegradation data, the porous metal oxides nanowires exhibit significantly photocatalytic activity for degrading tetracycline (TC). Furthermore, the porous Fe2O3 nanowires show the best photocatalytic performance among all the samples.

  2. Characteristics of Molten Alloys as Anodes in Solid Oxide Fuel Cells

    SciTech Connect

    Javadekar, Ashay; Jayakumar, Abhimanyu; Gorte, R. J.; Vohs, J. M.; Buttrey, D. J.

    2011-11-01

    Molten alloys with 50-mol% In-Sb, Sn-Sb, Sb-Bi, and Sb-Pb were examined as anodes for solid oxide fuel cells at 973 K. The cells were operated in the battery mode, without added fuel, in order to understand the oxidation characteristics of these alloys at electrolyte interfaces. Cells using 50-mol% In-Sb and Sn-Sb mixtures exhibited open-circuit voltages (OCV) of 1.0 and 0.93 V, values that are identical to that of cell with pure In and Sn respectively. Also similar to the pure In and Sn anodes, the impedances of these cells were initially low but increased dramatically after drawing a small amount of charge, implying formation of In₂O₃ and SnO₂ layers at the electrolyte interface. The 50-mol% Sb-Bi cell had an OCV of 0.73 V initially, close to the OCV observed with pure Sb. The OCV remained constant until a charge identical to that required for oxidation of all the Sb had been passed, after which the OCV dropped to 0.43 V, similar to the value for pure Bi. SEM analysis of the cell after conversion of the Sb showed two distinct phases, with metallic Bi at the bottom and Sb₂O₃ at the top. The electrochemical oxidation of 50-mol% Sb-Pb alloys exhibited an OCV that changed continuously with conversion, from 0.73 V initially to 0.67 V following the addition of charge corresponding to oxidation of 120% the Sb. The total cell impedance remained low for this entire period. EDS measurements on the sectioned Sb-Pb cell suggested that both Sb and Pb were oxidized simultaneously to form a mixed oxide of Pb and Sb.

  3. Cerium oxide coated anodes for aluminum electrowinning: Topical report, October 1, 1986-June 30, 1987

    SciTech Connect

    Walker, J. K.

    1987-12-01

    Because of the cost of building and maintaining a carbon anode plant and the energy penalties associated with the use of carbon anodes in the production of aluminum, the use of inert anodes has long been proposed. Various cermet anodes have been investigated. In this paper, tests on a material, cerium oxyfluoride (CEROX), deposited in situ as an anode, are reported. (JDH)

  4. Investigation of humidity-dependent size control of local anodic oxidation on graphene by using atomic force microscopy

    NASA Astrophysics Data System (ADS)

    Ko, Seoknam; Lee, Seong jun; Son, Maengho; Ahn, Doyeol; Lee, Seung-Woong

    2015-02-01

    We demonstrate nanoscale local anodic oxidation (LAO) patterning on few-layer graphene by using an atomic force microscope (AFM) at room temperature under a normal atmosphere. We focus on the humidity dependency of nanoscale oxidation of graphene. The relations between the oxidation size and the setting values of the AFM, such as the set point, tip speed, and the humidity, are observed. By changing these values, proper parameters were found to produce features with on-demand size. This technique provides an easy way for graphene oxide lithography without any chemical resists. We obtained oxidation sizes down to 50 nm with a 6-nm-high oxide barrier line by using a 0.1- μm/s tip scanning speed. We also obtained micrometer-sized symbols on a graphene flake. We attribute the bumps of oxidized graphene in the graphene layer to local anodic oxidation on graphenes surface and to an incorporation of oxygen ions into the graphene lattice.

  5. Tin nanoparticles encapsulated in porous multichannel carbon microtubes: preparation by single-nozzle electrospinning and application as anode material for high-performance Li-based batteries.

    PubMed

    Yu, Yan; Gu, Lin; Zhu, Changbao; van Aken, Peter A; Maier, Joachim

    2009-11-11

    Tin nanoparticles encapsulated in porous multichannel carbon microtubes (denoted as SPMCTs) were prepared by carbonization of electrospun PAN-PMMA-tin octoate nanofibers fabricated using a single-nozzle electrospinning technique. This material exhibited excellent characteristics for lithium ion battery anode applications in terms of reversible capacities, cycling performance, and rate capability. Undertaking such a production configuration allows the long-existing problem of obtaining a high packing density of tin particles while retaining sufficient spare space to buffer the volume variation during lithium alloying and dealloying processes to be properly addressed. Furthermore, the porous carbon shell preserves both the mechanical and chemical stability of the function-active Sn metal, which also serves as a highly conductive medium allowing Li(+) to access. PMID:19886691

  6. Anodic Deposition of a Robust Iridium-Based Water-Oxidation Catalyst from Organometallic Precursors

    SciTech Connect

    Blakemore, James D; Schley, Nathan D; Olack, G.; Incarvito, Christopher D; Brudvig, Gary W; Crabtree, Robert H

    2011-01-01

    Artificial photosynthesis, modeled on natural light-driven oxidation of water in Photosystem II, holds promise as a sustainable source of reducing equivalents for producing fuels. Few robust water-oxidation catalysts capable of mediating this difficult four-electron, four-proton reaction have yet been described. We report a new method for generating an amorphous electrodeposited material, principally consisting of iridium and oxygen, which is a robust and long-lived catalyst for water oxidation, when driven electrochemically. The catalyst material is generated by a simple anodic deposition from Cp*Ir aqua or hydroxo complexes in aqueous solution. This work suggests that organometallic precursors may be useful in electrodeposition of inorganic heterogeneous catalysts.

  7. The impact of NiO on microstructure and electrical property of solid oxide fuel cell anode

    PubMed Central

    Li, Yan; Luo, Zhong-yang; Yu, Chun-jiang; Luo, Dan; Xu, Zhu-an; Cen, Ke-fa

    2005-01-01

    Ni-Ce0.8Sm0.2O1.9 (Ni-SDC) cermet was selected as anode material for reduced temperature (800 °C) solid oxide fuel cells in this study. The influence of NiO powder fabrication methods for Ni-SDC cermets on the electrode performance was investigated so that the result obtained can be applied to make high-quality anode. Three kinds of NiO powder were synthesized with a fourth kind being available in the market. Four types of anode precursors were fabricated with these NiO powders and Ce0.8Sm0.2O1.9 (SDC), and then were reduced to anode wafers for sequencing measurement. The electrical conductivity of the anodes was measured and the effect of microstructure was investigated. It was found that the anode electrical conductivity depends strongly on the NiO powder morphologies, microstructure of the cermet anode and particle sizes, which are decided by NiO powder preparation technique. The highest electrical conductivity is obtained for anode cermets with NiO powder synthesized by NiCO3·2Ni(OH)2·4H2O or Ni(NO3)2·6H2O decomposition technique. PMID:16252348

  8. The impact of NiO on microstructure and electrical property of solid oxide fuel cell anode.

    PubMed

    Li, Yan; Luo, Zhong-yang; Yu, Chun-jiang; Luo, Dan; Xu, Zhu-an; Cen, Ke-fa

    2005-11-01

    Ni-Ce(0.8)Sm(0.2)O(1.9) (Ni-SDC) cermet was selected as anode material for reduced temperature (800 degrees C) solid oxide fuel cells in this study. The influence of NiO powder fabrication methods for Ni-SDC cermets on the electrode performance was investigated so that the result obtained can be applied to make high-quality anode. Three kinds of NiO powder were synthesized with a fourth kind being available in the market. Four types of anode precursors were fabricated with these NiO powders and Ce(0.8)Sm(0.2)O(1.9) (SDC), and then were reduced to anode wafers for sequencing measurement. The electrical conductivity of the anodes was measured and the effect of microstructure was investigated. It was found that the anode electrical conductivity depends strongly on the NiO powder morphologies, microstructure of the cermet anode and particle sizes, which are decided by NiO powder preparation technique. The highest electrical conductivity is obtained for anode cermets with NiO powder synthesized by NiCO(3).2Ni(OH)(2).4H(2)O or Ni(NO(3))(2).6H(2)O decomposition technique. PMID:16252348

  9. Anodization control for barrier-oxide thinning and 3D interconnected pores and direct electrodeposition of nanowire networks on native aluminium substrates.

    PubMed

    Gillette, Eleanor; Wittenberg, Stefanie; Graham, Lauren; Lee, Kwijong; Rubloff, Gary; Banerjee, Parag; Lee, Sang Bok

    2015-02-01

    Here we report a strategy for combining techniques for pore branching and barrier layer thinning to produce 3D porous anodized aluminum oxide films with direct ohmic contact to the native aluminum. This method provides an example of a rationally designed template which need not be removed from the aluminum, but which is also not constrained to traditional 2D pore geometry. We first demonstrate the barrier layer removal and pore branching techniques independently, and then combine them to produce free standing arrays of interconnected Ni nanostructures. Nickel nanostructures are deposited directly onto the aluminum to demonstrate the success of the structural modification, and showcase the potential for these films to be used as templates. This approach is the first to demonstrate the design and execution of multiple pore modification techniques in the same membrane, and demonstrates the first directly deposited 3D structures on aluminum substrates. PMID:25562070

  10. Porous silicon as a substrate material for potentiometric biosensors

    NASA Astrophysics Data System (ADS)

    Thust, Marion; Schöning, M. J.; Frohnhoff, S.; Arens-Fischer, R.; Kordos, P.; Lüth, H.

    1996-01-01

    For the first time porous silicon has been investigated for the purpose of application as a substrate material for potentiometric biosensors operating in aqueous solutions. Porous silicon was prepared from differently doped silicon substrates by a standard anodic etching process. After oxidation, penicillinase, an enzyme sensitive to penicillin, was bound to the porous structure by physical adsorption. To characterize the electrochemical properties of the so build up penicillin biosensor, capacitance - voltage (C - V) measurements were performed on these field-effect structures.

  11. Simulation of the reduction process of solid oxide fuel cell composite anode based on phase field method

    NASA Astrophysics Data System (ADS)

    Jiao, Zhenjun; Shikazono, Naoki

    2016-02-01

    It is known that the reduction process influences the initial performances and durability of nickel-yttria-stabilized zirconia composite anode of the solid oxide fuel cell. In the present study, the reduction process of nickel-yttria stabilized zirconia composite anode is simulated based on the phase field method. An three-dimensional reconstructed microstructure of nickel oxide-yttria stabilized zirconia composite obtained by focused ion beam-scanning electron microscopy is used as the initial microstructure for the simulation. Both reduction of nickel oxide and nickel sintering mechanisms are considered in the model. The reduction rates of nickel oxide at different interfaces are defined based on the literature data. Simulation results are qualitatively compared to the experimental anode microstructures with different reduction temperatures.

  12. Quantitative analysis of solid oxide fuel cell anode microstructure change during redox cycles

    NASA Astrophysics Data System (ADS)

    Shimura, Takaaki; Jiao, Zhenjun; Hara, Shotaro; Shikazono, Naoki

    2014-12-01

    In the present study, correlation between solid oxide fuel cell anode microstructure and electrochemical performance during redox cycles was investigated. Electrolyte-support cell with nickel/yttria stabilized zirconia composite anode was prepared and tested under discharge process with redox cycles. Redox treatment was basically conducted every 20 h during discharge process. Polarization resistance decreased just after redox treatment and increased during discharge process. Enhancement of cell performance after every redox cycles and faster degradation in the following discharge process were observed. Polarization resistance gradually increased as redox cycles were repeated. Focused ion beam-scanning electron microscopy (FIB-SEM) observation was conducted for reconstructing the three dimensional microstructures of the tested samples. From the three dimensional microstructure reconstruction, it is found that the shape of nickel particle got thinner and complicated after redox cycles. Triple phase boundary (TPB) length increased after redox treatment and decreased after discharge process. This TPB change was highly associated with Ni connectivity and Ni specific surface area. These microstructure changes are consistent with the change of cell performance enhancement after redox treatment and degradation after discharge process. However, TPB length density kept on increasing as redox cycles are repeated, which is inconsistent with the gradual degradation of anode performance.

  13. Ru nanostructure fabrication using an anodic aluminum oxide nanotemplate and highly conformal Ru atomic layer deposition.

    PubMed

    Kim, Woo-Hee; Park, Sang-Joon; Son, Jong-Yeog; Kim, Hyungjun

    2008-01-30

    We fabricated metallic nanostructures directly on Si substrates through a hybrid nanoprocess combining atomic layer deposition (ALD) and a self-assembled anodic aluminum oxide (AAO) nanotemplate. ALD Ru films with Ru(DMPD)(EtCp) as a precursor and O(2) as a reactant exhibited high purity and low resistivity with negligible nucleation delay and low roughness. These good growth characteristics resulted in the excellent conformality for nanometer-scale vias and trenches. Additionally, AAO nanotemplates were fabricated directly on Si and Ti/Si substrates through a multiple anodization process. AAO nanotemplates with various hole sizes (30-100 nm) and aspect ratios (2:1-20:1) were fabricated by controlling the anodizing process parameters. The barrier layers between AAO nanotemplates and Si substrates were completely removed by reactive ion etching (RIE) using BCl(3) plasma. By combining the ALD Ru and the AAO nanotemplate, Ru nanostructures with controllable sizes and shapes were prepared on Si and Ti/Si substrates. The Ru nanowire array devices as a platform for sensor devices exhibited befitting properties of good ohmic contact and high surface/volume ratio. PMID:21817499

  14. Origin of the bottlenecks in preparing anodized aluminum oxide (AAO) templates on ITO glass.

    PubMed

    Foong, Thelese R B; Sellinger, Alan; Hu, Xiao

    2008-11-25

    Nanoporous anodic alumina (AAO) templates are routinely created with ease on substrates, particularly Si wafers. However, the inability to stabilize Al anodization on indium tin oxide (ITO) glass is a key stumbling block that has prevented AAO-assisted deposition of nanomaterial arrays extending from ITO that are attractive for a range of opto-electronic applications (e.g., solar cells and photonic devices). We report on the processing of stable AAO templates directly on ITO substrates by utilizing an ultrathin (0.3 nm) adhesion/passivation layer of Ti between ITO and Al. Precise control of the Ti layer thickness to within the subnanometer (0.2-0.5 nm) range is essential for the anodization process for two factors: (1) to prevent the delamination of Al and destruction of ITO; and (2) to prevent the formation of thick barrier layers at the bottom of the pore channels, which prevent pore connectivity to the conductive ITO substrate. We explore the complex correlation between the electrical properties of substrates (and interlayers) and barrier layer formation and further highlight the criteria for successful barrier layer removal. PMID:19206390

  15. Improved coking resistance of direct ethanol solid oxide fuel cells with a Ni-Sx anode

    NASA Astrophysics Data System (ADS)

    Yan, Ning; Luo, Jing-Li; Chuang, Karl T.

    2014-03-01

    In this study, the coking resistance of anode supported direct ethanol solid oxide fuel cell with a Ni-Sx anode was investigated comparatively with the conventional cell using pure Ni catalyst. The surface catalytic properties of Ni were manipulated via depositing a layer of S atoms. It was confirmed that on the surface of Ni, a combination of S monolayer and elemental S was formed without producing Ni3S2 phase. The developed Ni-Sx cell exhibited a significantly improved coke resistivity in ethanol feed while maintaining an adequately high performance. The S species on Ni enabled the suppression of the coke formation as well as the alleviation of the metal dusting effect of the anode structure. After operating in ethanol fuel for identical period of time at 850 °C, a maximum power density of 400 mW cm-2 was sustained whereas the conventional cell performance decreased to less than 40 mW cm-2 from the original 704 mW cm-2. In an optimized stability test, the Ni-Sx cell operated at 750 °C for more than 22 h until the fuel drained without any degradation.

  16. Effect of Processing Parameters on Pore Structure and Thickness of Anodic Aluminum Oxide (AAO) Tubular Membranes.

    PubMed

    Belwalkar, A; Grasing, E; Van Geertruyden, W; Huang, Z; Misiolek, W Z

    2008-07-01

    Nanoporous anodic aluminum oxide (AAO) tubular membranes were fabricated from aluminum alloy tubes in sulfuric and oxalic acid electrolytes using a two-step anodization process. The membranes were investigated for characteristics such as pore size, interpore distance and thickness by varying applied voltage and electrolyte concentration. Morphology of the membranes was examined using light optical and scanning electron microscopy and characterized using ImageJ software. Results showed that membranes having narrow pore size and uniform pore distribution with parallel channel arrays were obtained. The pore sizes were ranging from 14 to 24 nm and the wall thicknesses as high as 76 microm. It was found that the pore size increased in direct proportion with the applied voltage and inversely with the electrolyte concentration while the interpore distance increased linearly with the applied voltage. It was also observed that increase in acid concentration increased tubular membrane wall thickness that improved mechanical handling. By using anodic alumina technology, robust ceramic tubes with uniformly distributed pore-structure and parallel nano-channels of lengths and sizes practical for industrial applications were reliably produced in quantity. PMID:19578471

  17. Accelerated creep in solid oxide fuel cell anode supports during reduction

    NASA Astrophysics Data System (ADS)

    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.

  18. Effect of Processing Parameters on Pore Structure and Thickness of Anodic Aluminum Oxide (AAO) Tubular Membranes

    PubMed Central

    Belwalkar, A.; Grasing, E.; Huang, Z.; Misiolek, W.Z.

    2008-01-01

    Nanoporous anodic aluminum oxide (AAO) tubular membranes were fabricated from aluminum alloy tubes in sulfuric and oxalic acid electrolytes using a two-step anodization process. The membranes were investigated for characteristics such as pore size, interpore distance and thickness by varying applied voltage and electrolyte concentration. Morphology of the membranes was examined using light optical and scanning electron microscopy and characterized using ImageJ software. Results showed that membranes having narrow pore size and uniform pore distribution with parallel channel arrays were obtained. The pore sizes were ranging from 14 to 24 nm and the wall thicknesses as high as 76 µm. It was found that the pore size increased in direct proportion with the applied voltage and inversely with the electrolyte concentration while the interpore distance increased linearly with the applied voltage. It was also observed that increase in acid concentration increased tubular membrane wall thickness that improved mechanical handling. By using anodic alumina technology, robust ceramic tubes with uniformly distributed pore-structure and parallel nano-channels of lengths and sizes practical for industrial applications were reliably produced in quantity. PMID:19578471

  19. Vanadium Sulfide on Reduced Graphene Oxide Layer as a Promising Anode for Sodium Ion Battery.

    PubMed

    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. PMID:26328897

  20. Porous Iron Oxide Ribbons Grown on Graphene for High-Performance Lithium Storage

    PubMed Central

    Yang, Shubin; Sun, Yi; Chen, Long; Hernandez, Yenny; Feng, Xinliang; Müllen, Klaus

    2012-01-01

    A well-designed nanostructure of transition metal oxides has been regarded as a key to solve their problems of large volume changes during lithium insertion-desertion processes which are associated with pulverization of the electrodes and rapid capacity decay. Here we report an effective approach for the fabrication of porous iron oxide ribbons by controlling the nucleation and growth of iron precursor onto the graphene surface and followed by an annealing treatment. The resultant iron oxide ribbons possess large aspect ratio, porous structure, thin feature and enhanced open-edges. These characteristics are favorable for the fast diffusion of lithium ions and electrons, and meanwhile can effectively accommodate the volume change of iron oxides during the cycling processes. As a consequence, the graphene-induced porous iron oxide ribbons exhibit a high reversible capacity and excellent cycle stability for lithium storage. PMID:22645643

  1. Metal-organic framework derived Fe2O3@NiCo2O4 porous nanocages as anode materials for Li-ion batteries.

    PubMed

    Huang, Gang; Zhang, Leilei; Zhang, Feifei; Wang, Limin

    2014-05-21

    Metal-organic frameworks (MOFs) with high surface areas and uniform microporous structures have shown potential application in many fields. Here we report a facial strategy to synthesize Fe2O3@NiCo2O4 porous nanocages by annealing core-shell Co3[Fe(CN)6]2@Ni3[Co(CN)6]2 nanocubes in air. The obtained samples have been systematically characterized by XRD, SEM, TEM and N2 adsorption-desorption analysis. The results show that the Fe2O3@NiCo2O4 porous nanocages have an average diameter of 213 nm and a shell thickness of about 30 nm. As anode materials for Li-ion batteries, the Fe2O3@NiCo2O4 porous nanocages exhibit a high initial discharge capacity of 1311.4 mA h g(-1) at a current density of 100 mA g(-1) (about 0.1 C). The capacity is retained at 1079.6 mA h g(-1) after 100 cycles. The synergistic effect of the different components and the porous hollow structure contributes to the outstanding performance of the composite electrode. PMID:24730026

  2. A 3D Porous Architecture of Si/graphene Nanocomposite as High-performance Anode Materials for Li-ion Batteries

    SciTech Connect

    Xin X.; Zhu Y.; Zhou, X.; Wang, F.; Yao, X.; Xu, X.; Liu, Z.

    2012-04-28

    A 3D porous architecture of Si/graphene nanocomposite has been rationally designed and constructed through a series of controlled chemical processes. In contrast to random mixture of Si nanoparticles and graphene nanosheets, the porous nanoarchitectured composite has superior electrochemical stability because the Si nanoparticles are firmly riveted on the graphene nanosheets through a thin SiO{sub x} layer. The 3D graphene network enhances electrical conductivity, and improves rate performance, demonstrating a superior rate capability over the 2D nanostructure. This 3D porous architecture can deliver a reversible capacity of {approx}900 mA h g{sup -1} with very little fading when the charge rates change from 100 mA g{sup -1} to 1 A g{sup -1}. Furthermore, the 3D nanoarchitechture of Si/graphene can be cycled at extremely high Li{sup +} extraction rates, such as 5 A g{sup -1} and 10 A g{sup -1}, for over than 100 times. Both the highly conductive graphene network and porous architecture are considered to contribute to the remarkable rate capability and cycling stability, thereby pointing to a new synthesis route to improving the electrochemical performances of the Si-based anode materials for advanced Li-ion batteries.

  3. Aptamer-modified anodized aluminum oxide-based capacitive sensor for the detection of bisphenol A

    NASA Astrophysics Data System (ADS)

    Kang, Bongkeun; Kim, Joo Hyoung; Kim, Soyoun; Yoo, Kyung-Hwa

    2011-02-01

    We describe a rapid, sensitive, and low-cost method to detect bisphenol A (BPA) using an anodized aluminum oxide-based capacitive sensor. BPA is detected by measuring the change in capacitance caused by the biospecific binding of BPA with a BPA aptamer that is immobilized on the electrode surface. For a solution containing 100 pM BPA, the capacitance decreased by approximately 3%. In addition, we fabricated a capacitive sensor array and demonstrated that BPA in environmental samples can be measured using our capacitive sensor.

  4. Fabrication of High power, High-Efficiency Linear Array Diode Lasers by Pulse Anodic Oxidation

    NASA Astrophysics Data System (ADS)

    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.

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

    NASA Astrophysics Data System (ADS)

    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.

  6. Surface and interface analysis of poly-hydroxyethylmethacrylate-coated anodic aluminium oxide membranes

    NASA Astrophysics Data System (ADS)

    Ali, Nurshahidah; Duan, Xiaofei; Jiang, Zhong-Tao; Goh, Bee Min; Lamb, Robert; Tadich, Anton; Poinern, Gérrard Eddy Jai; Fawcett, Derek; Chapman, Peter; Singh, Pritam

    2014-01-01

    The surface and interface of poly (2-hydroxyethylmethacrylate) (PHEMA) and anodic aluminium oxide (AAO) membranes were comprehensively investigated using Near Edge X-ray Absorption Fine Structure (NEXAFS) spectroscopy. It was found that 1s→π* (Cdbnd O) and 1s→σ* (Csbnd O) transitions were dominant on the surface of both bulk PHEMA polymer and PHEMA-surface coated AAO (AAO-PHEMA) composite. Findings from NEXAFS, Fourier-Transform Infrared (FTIR) and X-ray Photoelectron Spectroscopy (XPS) analyses suggest the possibility of chemical interaction between carbon from the ester group of polymer and AAO membrane.

  7. Rayleigh instability in polymer thin films coated in the nanopores of anodic aluminum oxide templates.

    PubMed

    Tsai, Chia-Chan; Chen, Jiun-Tai

    2014-01-14

    We study the Rayleigh instability of polystyrene (PS) thin films coated in the nanopores of anodic aluminum oxide (AAO) templates. After thermal annealing, the surface of the PS thin films undulates and the nanostructures transform from nanotubes to Rayleigh-instability-induced nanostructures (short nanorods with encapsulated air bubbles). With longer annealing times, the nanostructures further transform to nanorods with longer lengths. PS samples with two different molecular weights (24 and 100 kg/mol) are used, and their instability transformation processes are compared. The morphology diagrams of the nanostructures at different stages are also constructed to elucidate the mechanism of the morphology transformation. PMID:24380368

  8. Impedance spectroscopy study of anodic growth of zirconium oxide film in NaOH medium

    NASA Astrophysics Data System (ADS)

    Pauporté, T.; Finne, J.; Lincot, D.

    2005-06-01

    The growth of anodic oxide films on zirconium metal has been followed up to 300 V by electrochemical impedance spectroscopy and scanning electron microscopy. The maximum layer thickness is 720 nm, the dielectric constant of the film is measured at 19.5 and the growth constant is 2.4 nm V-1. Above 50 V, the presence of two impedance relaxations between 1 Hz and 200 kHz reveals a bilayered structure. This may be a consequence of a lower resistivity of the outer layer induced by some electrolytic solution infiltration into film defects.

  9. Anodized Ti3SiC2 As an Anode Material for Li-ion Microbatteries.

    PubMed

    Tesfaye, Alexander T; Mashtalir, Olha; Naguib, Michael; Barsoum, Michel W; Gogotsi, Yury; Djenizian, Thierry

    2016-07-01

    We report on the synthesis of an anode material for Li-ion batteries by anodization of a common MAX phase, Ti3SiC2, in an aqueous electrolyte containing hydrofluoric acid (HF). The anodization led to the formation of a porous film containing anatase, a small quantity of free carbon, and silica. By varying the anodization parameters, various oxide morphologies were produced. The highest areal capacity was achieved by anodization at 60 V in an aqueous electrolyte containing 0.1 v/v HF for 3 h at room temperature. After 140 cycles performed at multiple applied current densities, an areal capacity of 380 μAh·cm(-2) (200 μA·cm(-2)) has been obtained, making this new material, free of additives and binders, a promising candidate as a negative electrode for Li-ion microbatteries. PMID:27282275

  10. Stability of Chromium Carbide/Chromium Oxide Based Porous Ceramics in Supercritical Water

    NASA Astrophysics Data System (ADS)

    Dong, Ziqiang

    This research was aimed at developing porous ceramics as well as ceramic-metal composites that can be potentially used in Gen-IV supercritical water reactors (SCWR). The research mainly includes two parts: 1) fabricating and engineering the porous ceramics and porous ceramic-metal composite; 2) Evaluating the stability of the porous ceramics in SCW environments. Reactive sintering in carbonaceous environments was used to fabricate porous Cr3C2/Cr2O3-based ceramic. A new process consisting of freeze casting and reactive sintering has also been successfully developed to fabricate highly porous Cr3C 2 ceramics with multiple interconnected pores. Various amounts of cobalt powders were mixed with ceramic oxides in order to modify the porous structure and property of the porous carbide obtained by reactive sintering. The hardness of the M(Cr,Co)7C3-Co composite has been evaluated and rationalized based on the solid solution of cobalt in the ceramic phase, the composite effect of soft Co metal and the porous structure of the ceramic materials. Efforts have also been made in fabricating and evaluating interpenetrating Cr3C2-Cu composites formed by infiltrating liquid copper into porous Cr3C2. The corrosion evaluation mainly focused on assessing the stability of porous Cr3C2 and Cr2O3 under various SCW conditions. The corrosion tests showed that the porous Cr3C 2 is stable in SCW at temperatures below 425°C. However, cracking and disintegrating of the porous Cr3C2 occurred when the SCW temperature increased above 425°C. Mechanisms of the corrosion attack were also investigated. The porous Cr2O3 obtained by oxidizing the porous Cr3C2 was exposed to various SCW environments. It was found that the stability of Cr 2O 3 was dependent on its morphology and the SCW testing conditions. Increasing SCW temperature increased the dissociation rate of the Cr2O 3. Adding proper amount of Y2O3 can increase the stability of the porous Cr2O3 in SCW. It was also concluded that decreasing

  11. Device performances of organic light-emitting diodes with indium tin oxide, gallium zinc oxide, and indium zinc tin oxide anodes deposited at room temperature.

    PubMed

    Lee, Changhun; Ko, Yoonduk; Kim, Youngsung

    2013-12-01

    Thin films of Indium tin oxide (ITO), Gallium zinc oxide (GZO), and Indium zinc tin oxide (IZTO) were deposited on glass substrates by pulsed direct current magnetron sputtering at room temperature. The structural, optical, and electrical properties of the films were investigated towards evaluating their applications as flexible anodes. IZTO films exhibited the lowest resistivity (6.3 x 10(-4) Omega cm). Organic light-emitting diodes (OLEDs) were fabricated using the ITO, GZO, and IZTO films as anode layers. The turn-on voltages at a current density of 4.5 mA/cm2, 5.5 mA/cm2, 6.5 mA/cm2 were 5.5 V, 13.7 V, and 4.7 V for the devices with ITO, GZO, and IZTO anodes, respectively. The best performance was observed with the IZTO film, indicating its suitability as an alternative material for conventional ITO anodes used in OLEDs and flexible displays. PMID:24266182

  12. Degradation of 1-hydroxy-2,4-dinitrobenzene from aqueous solutions by electrochemical oxidation: role of anodic material.

    PubMed

    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. PMID:24462986

  13. One-step through-mask electrodeposition of a porous structure composed of manganese oxide nanosheets with electrocatalytic activity for oxygen reduction

    SciTech Connect

    Fukuda, Masaki; Iida, Chihiro; Nakayama, Masaharu

    2009-06-03

    Potentiostatic electrolysis of a mixed aqueous solution of Bu{sub 4}NBr and MnSO{sub 4} at +1.0 V (vs. Ag/AgCl) on Pt electrode led to the oxidation of Br{sup -} and Mn{sup 2+} ions. X-ray photoelectron spectroscopy (XPS), atomic force microscopy (AFM), and X-ray diffraction (XRD) revealed that this anodic process was followed by the deposition of insulating crystals of bromide salt of Bu{sub 4}N{sup +} and the subsequent formation of layered manganese oxide in the interstitial spaces of the bromide grains already grown. Dissolution of the bromide crystals in water left a well-dispersed porous texture composed of manganese oxide nanosheets. The resulting MnO{sub x}-modified electrode exhibited a larger catalytic current for the reduction of oxygen in alkaline solution, compared to the bare Pt electrode.

  14. MOF-derived ultrafine MnO nanocrystals embedded in a porous carbon matrix as high-performance anodes for lithium-ion batteries.

    PubMed

    Zheng, Fangcai; Xia, Guoliang; Yang, Yang; Chen, Qianwang

    2015-06-01

    Although MnO has been demonstrated to be a promising anode material for lithium-ion batteries (LIBs) in terms of its high theoretical capacity (755 mA h g(-1)), comparatively low voltage hysteresis (<0.8 V), low cost, and environmental benignity, the application of MnO as a practical electrode material is still hindered by many obstacles, including poor cycling stability and huge volume expansion during the charge/discharge process. Herein, we report a facile and scalable metal-organic framework-derived route for the in situ fabrication of ultrafine MnO nanocrystals encapsulated in a porous carbon matrix, where nanopores increase active sites to store redox ions and enhance ionic diffusivity to encapsulated MnO nanocrystals. As an anode material for lithium-ion batteries (LIBs), these MnO@C composites exhibited a high reversible specific capacity of 1221 mA h g(-1) after 100 cycles at a current density of 100 mA g(-1). The excellent electrochemical performance can be attributed to their unique structure with MnO nanocrystals dispersed uniformly inside a porous carbon matrix, which can largely enhance the electrical conductivity and effectively avoid the aggregation of MnO nanocrystals, and relieve the strain caused by the volumetric change during the charge/discharge process. This facile and economical strategy will extend the scope of metal-organic framework-derived synthesis for other materials in energy storage applications. PMID:25955439

  15. Treatment of synthetic urine by electrochemical oxidation using conductive-diamond anodes.

    PubMed

    Dbira, Sondos; Bensalah, Nasr; Bedoui, Ahmed; Cañizares, Pablo; Rodrigo, Manuel A

    2015-04-01

    In this work, the electrochemical oxidation of synthetic urine by anodic oxidation using boron-doped diamond as anode and stainless steel as cathode was investigated. Results show that complete depletion of chemical oxygen demand (COD) and total organic carbon (TOC) can be attained regardless of the current density applied in the range 20-100 mA cm(-2). Oxalic and oxamic acids, and, in lower concentrations, creatol and guanidine were identified as the main intermediates. Chloride ions play a very important role as mediators and contribute not only to obtain a high efficiency in the removal of the organics but also to obtain an efficient removal of nitrogen by the transformation of the various raw nitrogen species into gaseous nitrogen through chloramine formation. The main drawback of the technology is the formation of chlorates and perchlorates as final chlorine products. The increase of current density from 20 to 60 mA cm(-2) led to an increase in the rate of COD and TOC removals although the process becomes less efficient in terms of energy consumption (removals of COD and TOC after applying 18 Ah dm(-3) were 93.94 and 94.94 %, respectively, at 20 mA cm(-2) and 89.17 and 86.72 %, respectively, at 60 mA cm(-2)). The most efficient conditions are low current densities and high temperature reaching total mineralization at an applied charge as low as 20 kAh m(-3). This result confirmed that the electrolysis using diamond anodes is a very interesting technology for the treatment of urine. PMID:25399531

  16. Porous graphene oxide/carboxymethyl cellulose monoliths, with high metal ion adsorption.

    PubMed

    Zhang, Yongli; Liu, Yue; Wang, Xinrui; Sun, Zhiming; Ma, Junkui; Wu, Tao; Xing, Fubao; Gao, Jianping

    2014-01-30

    Orderly porous graphene oxide/carboxymethyl cellulose (GO/CMC) monoliths were prepared by a unidirectional freeze-drying method. The porous monoliths were characterized by Fourier transform infrared spectra, X-ray diffraction and scanning electron microscopy. Their properties including compressive strength and moisture adsorption were measured. The incorporation of GO changed the porous structure of the GO/CMC monoliths and significantly increased their compressive strength. The porous GO/CMC monoliths exhibited a strong ability to adsorb metal ions, and the Ni(2+) ions adsorbed on GO/CMC monolith were reduced by NaBH4 to obtain Ni GO/CMC monolith which could be used as catalyst in the reduction of 4-nitrophenol to 4-aminophenol. Since CMC is biodegradable and non-toxic, the porous GO/CMC monoliths are potential environmental adsorbents. PMID:24299788

  17. Preparation and electrochemical properties of multiwalled carbon nanotubes-nickel oxide porous composite for supercapacitors

    SciTech Connect

    Zheng Yanzhen; Zhang Milin . E-mail: dhyzyz@yahoo.com.cn; Gao Peng

    2007-09-04

    Porous nickel oxide/multiwalled carbon nanotubes (NiO/MWNTs) composite material was synthesized using sodium dodecyl phenyl sulfate as a soft template and urea as hydrolysis-controlling agent. Scanning electron microscopy (SEM) results show that the as-prepared nickel oxide nanoflakes aggregate to form a submicron ball shape with a porous structure, and the MWNTs with entangled and cross-linked morphology are well dispersed in the porous nickel oxide. The composite shows an excellent cycle performance at a high current of 2 A g{sup -1} and keeps a capacitance retention of about 89% over 200 charge/discharge cycles. A specific capacitance approximate to 206 F g{sup -1} has been achieved with NiO/MWNTs (10 wt.%) in 2 M KOH electrolyte. The electrical conductivity and the active sites for redox reaction of nickel oxide are significantly improved due to the connection of nickel nanoflakes by the long entangled MWNTs.

  18. Fuel cell anode configuration for CO tolerance

    DOEpatents

    Uribe, Francisco A.; Zawodzinski, Thomas A.

    2004-11-16

    A polymer electrolyte fuel cell (PEFC) is designed to operate on a reformate fuel stream containing oxygen and diluted hydrogen fuel with CO impurities. A polymer electrolyte membrane has an electrocatalytic surface formed from an electrocatalyst mixed with the polymer and bonded on an anode side of the membrane. An anode backing is formed of a porous electrically conductive material and has a first surface abutting the electrocatalytic surface and a second surface facing away from the membrane. The second surface has an oxidation catalyst layer effective to catalyze the oxidation of CO by oxygen present in the fuel stream where at least the layer of oxidation catalyst is formed of a non-precious metal oxidation catalyst selected from the group consisting of Cu, Fe, Co, Tb, W, Mo, Sn, and oxides thereof, and other metals having at least two low oxidation states.

  19. Electrochemical oxidation of biological pretreated and membrane separated landfill leachate concentrates on boron doped diamond anode

    NASA Astrophysics Data System (ADS)

    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.

  20. Degradation of thiamethoxam by the synergetic effect between anodic oxidation and Fenton reactions.

    PubMed

    Meijide, J; Gómez, J; Pazos, M; Sanromán, M A

    2016-12-01

    In this work, a comparative study using anodic oxidation, Fenton and electro-Fenton treatments was performed in order to determine the synergic effect for the removal of thiamethoxan. The results determined that electro-Fenton process showed high efficiency in comparison with Fenton or anodic oxidation. After that, this hybrid process was optimized and the influence of iron catalyst concentration and applied current intensity on the degradation and mineralization were evaluated. Degradation profiles were monitored by high performance liquid chromatography (HPLC) being satisfactorily described by pseudo-first order kinetic model. At the optimal experimental conditions (300mA and 0.2mM Fe(+2)), the complete degradation of thiamethoxam was achieved after 10min. On the other hand, mineralization of thiamethoxam was monitored by total organic carbon (TOC) decay reaching more than 92% of TOC removal after 8h. Furthermore, a plausible mineralization pathway for the thiamethoxam degradation was proposed based on the identification of by-products such as aromatic intermediates, carboxylic acids and inorganic ions released throughout electro-Fenton process. PMID:26968996