Aqueous processing of composite lithium ion electrode material

Energy Technology Data Exchange (ETDEWEB)

Li, Jianlin; Armstrong, Beth L.; Daniel, Claus; Wood, III, David L.

2017-06-20

A method of making a battery electrode includes the steps of dispersing an active electrode material and a conductive additive in water with at least one dispersant to create a mixed dispersion; treating a surface of a current collector to raise the surface energy of the surface to at least the surface tension of the mixed dispersion; depositing the dispersed active electrode material and conductive additive on a current collector; and heating the coated surface to remove water from the coating.

Polyanion-Type Electrode Materials for Sodium-Ion Batteries.

Science.gov (United States)

Ni, Qiao; Bai, Ying; Wu, Feng; Wu, Chuan

2017-03-01

Sodium-ion batteries, representative members of the post-lithium-battery club, are very attractive and promising for large-scale energy storage applications. The increasing technological improvements in sodium-ion batteries (Na-ion batteries) are being driven by the demand for Na-based electrode materials that are resource-abundant, cost-effective, and long lasting. Polyanion-type compounds are among the most promising electrode materials for Na-ion batteries due to their stability, safety, and suitable operating voltages. The most representative polyanion-type electrode materials are Na 3 V 2 (PO 4 ) 3 and NaTi 2 (PO 4 ) 3 for Na-based cathode and anode materials, respectively. Both show superior electrochemical properties and attractive prospects in terms of their development and application in Na-ion batteries. Carbonophosphate Na 3 MnCO 3 PO 4 and amorphous FePO 4 have also recently emerged and are contributing to further developing the research scope of polyanion-type Na-ion batteries. However, the typical low conductivity and relatively low capacity performance of such materials still restrict their development. This paper presents a brief review of the research progress of polyanion-type electrode materials for Na-ion batteries, summarizing recent accomplishments, highlighting emerging strategies, and discussing the remaining challenges of such systems.

Polyanion‐Type Electrode Materials for Sodium‐Ion Batteries

Science.gov (United States)

Ni, Qiao; Wu, Feng

2017-01-01

Sodium‐ion batteries, representative members of the post‐lithium‐battery club, are very attractive and promising for large‐scale energy storage applications. The increasing technological improvements in sodium‐ion batteries (Na‐ion batteries) are being driven by the demand for Na‐based electrode materials that are resource‐abundant, cost‐effective, and long lasting. Polyanion‐type compounds are among the most promising electrode materials for Na‐ion batteries due to their stability, safety, and suitable operating voltages. The most representative polyanion‐type electrode materials are Na3V2(PO4)3 and NaTi2(PO4)3 for Na‐based cathode and anode materials, respectively. Both show superior electrochemical properties and attractive prospects in terms of their development and application in Na‐ion batteries. Carbonophosphate Na3MnCO3PO4 and amorphous FePO4 have also recently emerged and are contributing to further developing the research scope of polyanion‐type Na‐ion batteries. However, the typical low conductivity and relatively low capacity performance of such materials still restrict their development. This paper presents a brief review of the research progress of polyanion‐type electrode materials for Na‐ion batteries, summarizing recent accomplishments, highlighting emerging strategies, and discussing the remaining challenges of such systems. PMID:28331782

Phosphate Framework Electrode Materials for Sodium Ion Batteries.

Science.gov (United States)

Fang, Yongjin; Zhang, Jiexin; Xiao, Lifen; Ai, Xinping; Cao, Yuliang; Yang, Hanxi

2017-05-01

Sodium ion batteries (SIBs) have been considered as a promising alternative for the next generation of electric storage systems due to their similar electrochemistry to Li-ion batteries and the low cost of sodium resources. Exploring appropriate electrode materials with decent electrochemical performance is the key issue for development of sodium ion batteries. Due to the high structural stability, facile reaction mechanism and rich structural diversity, phosphate framework materials have attracted increasing attention as promising electrode materials for sodium ion batteries. Herein, we review the latest advances and progresses in the exploration of phosphate framework materials especially related to single-phosphates, pyrophosphates and mixed-phosphates. We provide the detailed and comprehensive understanding of structure-composition-performance relationship of materials and try to show the advantages and disadvantages of the materials for use in SIBs. In addition, some new perspectives about phosphate framework materials for SIBs are also discussed. Phosphate framework materials will be a competitive and attractive choice for use as electrodes in the next-generation of energy storage devices.

Structure and Modification of Electrode Materials for Protein Electrochemistry.

Science.gov (United States)

Jeuken, Lars J C

The interactions between proteins and electrode surfaces are of fundamental importance in bioelectrochemistry, including photobioelectrochemistry. In order to optimise the interaction between electrode and redox protein, either the electrode or the protein can be engineered, with the former being the most adopted approach. This tutorial review provides a basic description of the most commonly used electrode materials in bioelectrochemistry and discusses approaches to modify these surfaces. Carbon, gold and transparent electrodes (e.g. indium tin oxide) are covered, while approaches to form meso- and macroporous structured electrodes are also described. Electrode modifications include the chemical modification with (self-assembled) monolayers and the use of conducting polymers in which the protein is imbedded. The proteins themselves can either be in solution, electrostatically adsorbed on the surface or covalently bound to the electrode. Drawbacks and benefits of each material and its modifications are discussed. Where examples exist of applications in photobioelectrochemistry, these are highlighted.

The rise of organic electrode materials for energy storage.

Science.gov (United States)

Schon, Tyler B; McAllister, Bryony T; Li, Peng-Fei; Seferos, Dwight S

2016-11-07

Organic electrode materials are very attractive for electrochemical energy storage devices because they can be flexible, lightweight, low cost, benign to the environment, and used in a variety of device architectures. They are not mere alternatives to more traditional energy storage materials, rather, they have the potential to lead to disruptive technologies. Although organic electrode materials for energy storage have progressed in recent years, there are still significant challenges to overcome before reaching large-scale commercialization. This review provides an overview of energy storage systems as a whole, the metrics that are used to quantify the performance of electrodes, recent strategies that have been investigated to overcome the challenges associated with organic electrode materials, and the use of computational chemistry to design and study new materials and their properties. Design strategies are examined to overcome issues with capacity/capacitance, device voltage, rate capability, and cycling stability in order to guide future work in the area. The use of low cost materials is highlighted as a direction towards commercial realization.

A polyoxovanadate as an advanced electrode material for supercapacitors.

Science.gov (United States)

Chen, Han-Yi; Wee, Grace; Al-Oweini, Rami; Friedl, Jochen; Tan, Kim Soon; Wang, Yuxi; Wong, Chui Ling; Kortz, Ulrich; Stimming, Ulrich; Srinivasan, Madhavi

2014-07-21

Polyoxovanadate Na(6)V(10)O(28) is investigated for the first time as electrode material for supercapacitors (SCs). The electrochemical properties of Na(6)V(10)O(28) electrodes are studied in Li(+) -containing organic electrolyte (1 M LiClO(4) in propylene carbonate) by galvanostatic charge/discharge and cyclic voltammetry in a three-electrode configuration. Na(6)V(10)O(28) electrodes exhibit high specific capacitances of up to 354 F g(-1). An asymmetric SC with activated carbon as positive electrode and Na(6)V(10)O(28) as negative electrode is fabricated and exhibits a high energy density of 73 Wh kg(-1) with a power density of 312 W kg(-1), which successfully demonstrates that Na(6)V(10)O(28) is a promising electrode material for high-energy SC applications. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Pseudocapacitive and hierarchically ordered porous electrode materials supercapacitors

Science.gov (United States)

Saruhan, B.; Gönüllü, Y.; Arndt, B.

2013-05-01

Commercially available double layer capacitors store energy in an electrostatic field. This forms in the form of a double layer by charged particles arranged on two electrodes consisting mostly of active carbon. Such double layer capacitors exhibit a low energy density, so that components with large capacity according to large electrode areas are required. Our research focuses on the development of new electrode materials to realize the production of electrical energy storage systems with high energy density and high power density. Metal oxide based electrodes increase the energy density and the capacitance by addition of pseudo capacitance to the static capacitance present by the double layer super-capacitor electrodes. The so-called hybrid asymmetric cell capacitors combine both types of energy storage in a single component. In this work, the production routes followed in our laboratories for synthesis of nano-porous and aligned metal oxide electrodes using the electrochemical and sputter deposition as well as anodization methods will be described. Our characterisation studies concentrate on electrodes having redox metal-oxides (e.g. MnOx and WOx) and hierarchically aligned nano-porous Li-doped TiO2-NTs. The material specific and electrochemical properties achieved with these electrodes will be presented.

A review of electrode materials for electrochemical supercapacitors.

Science.gov (United States)

Wang, Guoping; Zhang, Lei; Zhang, Jiujun

2012-01-21

In this critical review, metal oxides-based materials for electrochemical supercapacitor (ES) electrodes are reviewed in detail together with a brief review of carbon materials and conducting polymers. Their advantages, disadvantages, and performance in ES electrodes are discussed through extensive analysis of the literature, and new trends in material development are also reviewed. Two important future research directions are indicated and summarized, based on results published in the literature: the development of composite and nanostructured ES materials to overcome the major challenge posed by the low energy density of ES (476 references).

Advances in electrode materials for Li-based rechargeable batteries

Energy Technology Data Exchange (ETDEWEB)

Zhang, Hui [China Academy of Space Technology (CAST), Beijing (China); Mao, Chengyu [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Li, Jianlin [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Univ. of Tennessee, Knoxville, TN (United States); Chen, Ruiyong [Korea Inst. of Science and Technology (KIST), Saarbrucken (Germany); Saarland Univ., Saarbrucken (Germany)

2017-07-05

Rechargeable lithium-ion batteries store energy as chemical energy in electrode materials during charge and can convert the chemical energy into electrical energy when needed. Tremendous attention has been paid to screen electroactive materials, to evaluate their structural integrity and cycling reversibility, and to improve the performance of electrode materials. This review discusses recent advances in performance enhancement of both anode and cathode through nanoengineering active materials and applying surface coatings, in order to effectively deal with the challenges such as large volume variation, instable interface, limited cyclability and rate capability. We also introduce and discuss briefly the diversity and new tendencies in finding alternative lithium storage materials, safe operation enabled in aqueous electrolytes, and configuring novel symmetric electrodes and lithium-based flow batteries.

Electrode material comprising graphene-composite materials in a graphite network

Science.gov (United States)

Kung, Harold H.; Lee, Jung K.

2017-08-08

A durable electrode material suitable for use in Li ion batteries is provided. The material is comprised of a continuous network of graphite regions integrated with, and in good electrical contact with a composite comprising graphene sheets and an electrically active material, such as silicon, wherein the electrically active material is dispersed between, and supported by, the graphene sheets.

Functional materials in amperometric sensing polymeric, inorganic, and nanocomposite materials for modified electrodes

CERN Document Server

Seeber, Renato; Zanardi, Chiara

2014-01-01

Amperometric sensors, biosensors included, particularly rely on suitable electrode materials. Progress in material science has led to a wide variety of options that are available today. For the first time, these novel functional electrode coating materials are reviewed in this monograph, written by and for electroanalytical chemists. This includes intrinsically conducting, redox and ion-exchange polymers, metal and carbon nanostructures, silica based materials. Monolayers and relatively thick films are considered. The authors critically discuss preparation methods, in addition to chemical and

Unconventional supercapacitors from nanocarbon-based electrode materials to device configurations.

Science.gov (United States)

Liu, Lili; Niu, Zhiqiang; Chen, Jun

2016-07-25

As energy storage devices, supercapacitors that are also called electrochemical capacitors possess high power density, excellent reversibility and long cycle life. The recent boom in electronic devices with different functions in transparent LED displays, stretchable electronic systems and artificial skin has increased the demand for supercapacitors to move towards light, thin, integrated macro- and micro-devices with transparent, flexible, stretchable, compressible and/or wearable abilities. The successful fabrication of such supercapacitors depends mainly on the preparation of innovative electrode materials and the design of unconventional supercapacitor configurations. Tremendous research efforts have been recently made to design and construct innovative nanocarbon-based electrode materials and supercapacitors with unconventional configurations. We review here recent developments in supercapacitors from nanocarbon-based electrode materials to device configurations. The advances in nanocarbon-based electrode materials mainly include the assembly technologies of macroscopic nanostructured electrodes with different dimensions of carbon nanotubes/nanofibers, graphene, mesoporous carbon, activated carbon, and their composites. The electrodes with macroscopic nanostructured carbon-based materials overcome the issues of low conductivity, poor mechanical properties, and limited dimensions that are faced by conventional methods. The configurational design of advanced supercapacitor devices is presented with six types of unconventional supercapacitor devices: flexible, micro-, stretchable, compressible, transparent and fiber supercapacitors. Such supercapacitors display unique configurations and excellent electrochemical performance at different states such as bending, stretching, compressing and/or folding. For example, all-solid-state simplified supercapacitors that are based on nanostructured graphene composite paper are able to maintain 95% of the original capacity at

Electrode Materials for Lithium/Sodium-Ion Batteries

DEFF Research Database (Denmark)

Shen, Yanbin

2014-01-01

The synthesis of electrode materials for lithium/sodium ion batteries and their structural stability during lithium/sodium insertion/extraction are the two essential issues that have limited battery application in the fields requiring long cycle life and high safety. During her PhD studies, Yanbin...... Shen systematically investigated the controlled synthesis of electrode materials for lithium/sodium ion batteries. She also investigated their formation mechanisms and structural evolution during the operation of batteries using in situ/operando X-ray diffraction techniques. The research findings...... provide insights into formation mechanisms of Li4Ti5O12 anode material from both hydrothermal and solid-state reaction. The results also contribute to a thorough understanding of the intercalation and decay mechanisms of O3/P2 layered sodium cathode materials in sodium ion batteries....

Crystallic silver amalgam--a novel electrode material.

Science.gov (United States)

Danhel, Ales; Mansfeldova, Vera; Janda, Pavel; Vyskocil, Vlastimil; Barek, Jiri

2011-09-21

A crystallic silver amalgam was found to be a suitable working electrode material for voltammetric determination of electrochemically reducible organic nitro-compounds. Optimum conditions for crystal growth were found, the crystal surface was investigated by atomic force microscopy in tapping mode and single crystals were used for the preparation of quasi-cylindrical single crystal silver amalgam electrode (CAgAE). An electrochemical behavior of this alternative electrode material was investigated in aqueous media by direct current voltammetry, cyclic voltammetry (CV), differential pulse voltammetry (DPV) and adsorptive stripping voltammetry (AdSV) using 4-nitrophenol as a model compound. Applicable potential windows of the CAgAE were found comparable with those obtained at a hanging mercury drop electrode, providing high hydrogen overpotential, and polished silver solid amalgam electrode. Thanks to the smooth single crystal electrode surface, the effect of the passivation is not too pronounced, direct DPV determination of 100 μmol l(-1) of 4-nitrophenol at CAgAEs in 0.2 mol l(-1) acetate buffer pH 4.8 provides a RSD around 1.5% (n = 15). DPV calibration curves of 4-nitrophenol are linear in the whole concentration range 1-100 μmol l(-1) with a limit of quantification of 1.5 μmol l(-1). The attempt to increase sensitivity by application of AdSV was not successful. The mechanism of 4-nitrophenol reduction at CAgAE was investigated by CV.

Effect of oxidation of carbon material on suspension electrodes for flow electrode capacitive deionization.

Science.gov (United States)

Hatzell, Kelsey B; Hatzell, Marta C; Cook, Kevin M; Boota, Muhammad; Housel, Gabrielle M; McBride, Alexander; Kumbur, E Caglan; Gogotsi, Yury

2015-03-03

Flow electrode deionization (FCDI) is an emerging area for continuous and scalable deionization, but the electrochemical and flow properties of the flow electrode need to be improved to minimize energy consumption. Chemical oxidation of granular activated carbon (AC) was examined here to study the role of surface heteroatoms on rheology and electrochemical performance of a flow electrode (carbon slurry) for deionization processes. Moreover, it was demonstrated that higher mass densities could be used without increasing energy for pumping when using oxidized active material. High mass-loaded flow electrodes (28% carbon content) based on oxidized AC displayed similar viscosities (∼21 Pa s) to lower mass-loaded flow electrodes (20% carbon content) based on nonoxidized AC. The 40% increased mass loading (from 20% to 28%) resulted in a 25% increase in flow electrode gravimetric capacitance (from 65 to 83 F g(-1)) without sacrificing flowability (viscosity). The electrical energy required to remove ∼18% of the ions (desalt) from of the feed solution was observed to be significantly dependent on the mass loading and decreased (∼60%) from 92 ± 7 to 28 ± 2.7 J with increased mass densities from 5 to 23 wt %. It is shown that the surface chemistry of the active material in a flow electrode effects the electrical and pumping energy requirements of a FCDI system.

Fuel cell electrode interconnect contact material encapsulation and method

Science.gov (United States)

Derose, Anthony J.; Haltiner, Jr., Karl J.; Gudyka, Russell A.; Bonadies, Joseph V.; Silvis, Thomas W.

2016-05-31

A fuel cell stack includes a plurality of fuel cell cassettes each including a fuel cell with an anode and a cathode. Each fuel cell cassette also includes an electrode interconnect adjacent to the anode or the cathode for providing electrical communication between an adjacent fuel cell cassette and the anode or the cathode. The interconnect includes a plurality of electrode interconnect protrusions defining a flow passage along the anode or the cathode for communicating oxidant or fuel to the anode or the cathode. An electrically conductive material is disposed between at least one of the electrode interconnect protrusions and the anode or the cathode in order to provide a stable electrical contact between the electrode interconnect and the anode or cathode. An encapsulating arrangement segregates the electrically conductive material from the flow passage thereby, preventing volatilization of the electrically conductive material in use of the fuel cell stack.

Catoptric electrodes: transparent metal electrodes using shaped surfaces.

Science.gov (United States)

Kik, Pieter G

2014-09-01

An optical electrode design is presented that theoretically allows 100% optical transmission through an interdigitated metallic electrode at 50% metal areal coverage. This is achieved by redirection of light incident on embedded metal electrode lines to an angle beyond that required for total internal reflection. Full-field electromagnetic simulations using realistic material parameters demonstrate 84% frequency-averaged transmission for unpolarized illumination across the entire visible spectral range using a silver interdigitated electrode at 50% areal coverage. The redirection is achieved through specular reflection, making it nonresonant and arbitrarily broadband, provided the electrode width exceeds the optical wavelength. These findings could significantly improve the performance of photovoltaic devices and optical detectors that require high-conductivity top contacts.

Carbon materials modified by plasma treatment as electrodes for supercapacitors

Energy Technology Data Exchange (ETDEWEB)

Lota, Grzegorz; Frackowiak, Elzbieta [Institute of Chemistry and Technical Electrochemistry, Poznan University of Technology, Piotrowo 3, 60-965 Poznan (Poland); Tyczkowski, Jacek; Kapica, Ryszard [Technical University of Lodz, Faculty of Process and Environmental Engineering, Division of Molecular Engineering, Wolczanska 213, 90-924 Lodz (Poland); Lota, Katarzyna [Institute of Non-Ferrous Metals Branch in Poznan, Central Laboratory of Batteries and Cells, Forteczna 12, 61-362 Poznan (Poland)

2010-11-15

The carbon material was modified by RF plasma with various reactive gases: O{sub 2}, Ar and CO{sub 2}. Physicochemical properties of the final carbon products were characterized using different techniques such as gas adsorption method and XPS. Plasma modified materials enriched in oxygen functionalities were investigated as electrodes for supercapacitors in acidic medium. The electrochemical measurements have been carried out using cyclic voltammetry, galvanostatic charge/discharge and impedance spectroscopy. The electrochemical measurements have confirmed that capacity characteristics are closely connected with a type of plasma exposition. Modification processes have an influence on the kind and amount of surface functional groups in the carbon matrix. The moderate increase of capacity of carbon materials modified by plasma has been observed using symmetric two-electrode systems. Whereas investigations made in three-electrode system proved that the suitable selection of plasma modification parameters allows to obtain promising negative and positive electrode materials for supercapacitor application. (author)

Thick electrodes including nanoparticles having electroactive materials and methods of making same

Science.gov (United States)

Xiao, Jie; Lu, Dongping; Liu, Jun; Zhang, Jiguang; Graff, Gordon L.

2017-02-21

Electrodes having nanostructure and/or utilizing nanoparticles of active materials and having high mass loadings of the active materials can be made to be physically robust and free of cracks and pinholes. The electrodes include nanoparticles having electroactive material, which nanoparticles are aggregated with carbon into larger secondary particles. The secondary particles can be bound with a binder to form the electrode.

High Reversibility of Soft Electrode Materials in All-solid-state Batteries

Directory of Open Access Journals (Sweden)

Atsushi eSakuda

2016-05-01

Full Text Available All-solid-state batteries using inorganic solid electrolytes (SEs are considered to be ideal batteries for electric vehicles (EVs and plug-in hybrid electric vehicles (PHEVs because they are potentially safer than conventional lithium-ion batteries (LIBs. In addition, all-solid-state batteries are expected to have long battery lives owing to the inhibition of chemical side reactions because only lithium ions move through the typically used inorganic SEs. The development of high-energy (more than 300 Wh kg-1 secondary batteries has been eagerly anticipated for years. The application of high-capacity electrode active materials is essential for fabricating such batteries. Recently, we proposed metal polysulfides as new electrode materials. These materials show higher conductivity and density than sulfur, which is advantageous for fabricating batteries with relatively higher energy density. Lithium niobium sulfides, such as Li3NbS4, have relatively high density, conductivity, and rate capability among metal polysulfide materials, and batteries with these materials have capacities high enough to potentially exceed the gravimetric energy density of conventional LIBs.Favorable solid-solid contact between the electrode and electrolyte particles is a key factor for fabricating high performance all-solid-state batteries. Conventional oxide-based positive electrode materials tend to be given rise to cracks during fabrication and/or charge-discharge processes. Here we report all-solid-state cells using lithium niobium sulfide as a positive electrode material, where favorable solid-solid contact was established by using lithium sulfide electrode materials because of their high processability. Cracks were barely observed in the electrode particles in the all-solid-state cells before or after charging and discharging with a high capacity of approx. 400 mAh g-1, suggesting that the lithium niobium sulfide electrode charged and discharged without experiencing

Effect of top electrode material on radiation-induced degradation of ferroelectric thin film structures

Energy Technology Data Exchange (ETDEWEB)

Brewer, Steven J.; Bassiri-Gharb, Nazanin [G.W. Woodruff School of Mechanical Engineering, Georgia Institute of Technology, Atlanta, Georgia 30332 (United States); School of Materials Science and Engineering, Georgia Institute of Technology, Atlanta, Georgia 30332 (United States); Deng, Carmen Z.; Callaway, Connor P. [School of Materials Science and Engineering, Georgia Institute of Technology, Atlanta, Georgia 30332 (United States); Paul, McKinley K. [G.W. Woodruff School of Mechanical Engineering, Georgia Institute of Technology, Atlanta, Georgia 30332 (United States); Woodward Academy, College Park, Georgia 30337 (United States); Fisher, Kenzie J. [G.W. Woodruff School of Mechanical Engineering, Georgia Institute of Technology, Atlanta, Georgia 30332 (United States); Riverwood International Charter School, Atlanta, Georgia 30328 (United States); Guerrier, Jonathon E.; Jones, Jacob L. [Department of Materials Science and Engineering, North Carolina State University, Raleigh, North Carolina 27695 (United States); Rudy, Ryan Q.; Polcawich, Ronald G. [Army Research Laboratory, Adelphi, Maryland 20783 (United States); Glaser, Evan R.; Cress, Cory D. [Naval Research Laboratory, Washington, DC 20375 (United States)

2016-07-14

The effects of gamma irradiation on the dielectric and piezoelectric responses of Pb[Zr{sub 0.52}Ti{sub 0.48}]O{sub 3} (PZT) thin film stacks were investigated for structures with conductive oxide (IrO{sub 2}) and metallic (Pt) top electrodes. The samples showed, generally, degradation of various key dielectric, ferroelectric, and electromechanical responses when exposed to 2.5 Mrad (Si) {sup 60}Co gamma radiation. However, the low-field, relative dielectric permittivity, ε{sub r}, remained largely unaffected by irradiation in samples with both types of electrodes. Samples with Pt top electrodes showed substantial degradation of the remanent polarization and overall piezoelectric response, as well as pinching of the polarization hysteresis curves and creation of multiple peaks in the permittivity-electric field curves post irradiation. The samples with oxide electrodes, however, were largely impervious to the same radiation dose, with less than 5% change in any of the functional characteristics. The results suggest a radiation-induced change in the defect population or defect energy in PZT with metallic top electrodes, which substantially affects motion of internal interfaces such as domain walls. Additionally, the differences observed for stacks with different electrode materials implicate the ferroelectric–electrode interface as either the predominant source of radiation-induced effects (Pt electrodes) or the site of healing for radiation-induced defects (IrO{sub 2} electrodes).

Effects of Electrode Material on the Voltage of a Tree-Based Energy Generator.

Science.gov (United States)

Hao, Zhibin; Wang, Guozhu; Li, Wenbin; Zhang, Junguo; Kan, Jiangming

2015-01-01

The voltage between a standing tree and its surrounding soil is regarded as an innovative renewable energy source. This source is expected to provide a new power generation system for the low-power electrical equipment used in forestry. However, the voltage is weak, which has caused great difficulty in application. Consequently, the development of a method to increase the voltage is a key issue that must be addressed in this area of applied research. As the front-end component for energy harvesting, a metal electrode has a material effect on the level and stability of the voltage obtained. This study aimed to preliminarily ascertain the rules and mechanisms that underlie the effects of electrode material on voltage. Electrodes of different materials were used to measure the tree-source voltage, and the data were employed in a comparative analysis. The results indicate that the conductivity of the metal electrode significantly affects the contact resistance of the electrode-soil and electrode-trunk contact surfaces, thereby influencing the voltage level. The metal reactivity of the electrode has no significant effect on the voltage. However, passivation of the electrode materials markedly reduces the voltage. Suitable electrode materials are demonstrated and recommended.

Sulfur based electrode materials for secondary batteries

Science.gov (United States)

Hao, Yong

Developing next generation secondary batteries has attracted much attention in recent years due to the increasing demand of high energy and high power density energy storage for portable electronics, electric vehicles and renewable sources of energy. This dissertation investigates sulfur based advanced electrode materials in Lithium/Sodium batteries. The electrochemical performances of the electrode materials have been enhanced due to their unique nano structures as well as the formation of novel composites. First, a nitrogen-doped graphene nanosheets/sulfur (NGNSs/S) composite was synthesized via a facile chemical reaction deposition. In this composite, NGNSs were employed as a conductive host to entrap S/polysulfides in the cathode part. The NGNSs/S composite delivered an initial discharge capacity of 856.7 mAh g-1 and a reversible capacity of 319.3 mAh g-1 at 0.1C with good recoverable rate capability. Second, NGNS/S nanocomposites, synthesized using chemical reaction-deposition method and low temperature heat treatment, were further studied as active cathode materials for room temperature Na-S batteries. Both high loading composite with 86% gamma-S8 and low loading composite with 25% gamma-S8 have been electrochemically evaluated and compared with both NGNS and S control electrodes. It was found that low loading NGNS/S composite exhibited better electrochemical performance with specific capacity of 110 and 48 mAh g-1 at 0.1C at the 1st and 300th cycle, respectively. The Coulombic efficiency of 100% was obtained at the 300th cycle. Third, high purity rock-salt (RS), zinc-blende (ZB) and wurtzite (WZ) MnS nanocrystals with different morphologies were successfully synthesized via a facile solvothermal method. RS-, ZB- and WZ-MnS electrodes showed the capacities of 232.5 mAh g-1, 287.9 mAh g-1 and 79.8 mAh g-1 at the 600th cycle, respectively. ZB-MnS displayed the best performance in terms of specific capacity and cyclability. Interestingly, MnS electrodes

Nanostructured mesophase electrode materials: modulating charge-storage behavior by thermal treatment.

Science.gov (United States)

Kong, Hye Jeong; Kim, Saerona; Le, Thanh-Hai; Kim, Yukyung; Park, Geunsu; Park, Chul Soon; Kwon, Oh Seok; Yoon, Hyeonseok

2017-11-16

3D nanostructured carbonaceous electrode materials with tunable capacitive phases were successfully developed using graphene/particulate polypyrrole (PPy) nanohybrid (GPNH) precursors without a separate process for incorporating heterogeneous species. The electrode material, namely carbonized GPNHs (CGPNHs) featured a mesophase capacitance consisting of both electric double-layer (EDL) capacitive and pseudocapacitive elements at the molecular level. The ratio of EDL capacitive element to pseudocapacitive element (E-to-P) in the mesophase electrode materials was controlled by varying the PPy-to-graphite weight (P w /G w ) ratio and by heat treatment (T H ), which was demonstrated by characterizing the CGPNHs with elemental analysis, cyclic voltammetry, and a charge/discharge test. The concept of the E-to-P ratio (EPR) index was first proposed to easily identify the capacitive characteristics of the mesophase electrode using a numerical algorithm, which was reasonably consistent with the experimental findings. Finally, the CGPNHs were integrated into symmetric two-electrode capacitor cells, which rendered excellent energy and power densities in both aqueous and ionic liquid electrolytes. It is anticipated that our approach could be widely extended to fabricating versatile hybrid electrode materials with estimation of their capacitive characteristics.

Organic electrode materials for rechargeable lithium batteries

Energy Technology Data Exchange (ETDEWEB)

Liang, Yanliang; Tao, Zhanliang; Chen, Jun [Key Laboratory of Advanced Energy Materials Chemistry (Ministry of Education), Chemistry College, Nankai University, Tianjin (China)

2012-07-15

Organic compounds offer new possibilities for high energy/power density, cost-effective, environmentally friendly, and functional rechargeable lithium batteries. For a long time, they have not constituted an important class of electrode materials, partly because of the large success and rapid development of inorganic intercalation compounds. In recent years, however, exciting progress has been made, bringing organic electrodes to the attention of the energy storage community. Herein thirty years' research efforts in the field of organic compounds for rechargeable lithium batteries are summarized. The working principles, development history, and design strategies of these materials, including organosulfur compounds, organic free radical compounds, organic carbonyl compounds, conducting polymers, non-conjugated redox polymers, and layered organic compounds are presented. The cell performances of these materials are compared, providing a comprehensive overview of the area, and straightforwardly revealing the advantages/disadvantages of each class of materials. (Copyright copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

Electrode materials for an open-cycle MHD generator channel

International Nuclear Information System (INIS)

Telegin, G.P.; Romanov, A.I.; Akopov, F.A.; Gokhshtejn, Ya.P.; Rekov, A.I.

1983-01-01

The results of investigations, technological developments and tests of high temperature materials for MHD electrodes on the base of zirconium dioxide, stabilized with oxides of calcium, yttrium, neodymium, and dioxide of cerium, chromites, tamping masses from stabilized dioxide of zirconium, cermets are considered. It is established that binary and ternary solutions on the base of zirconium dioxide and alloyed chromites are the perspective materials for the MHD electrodes on pure fuel

Nickel-Tin Electrode Materials for Nonaqueous Li-Ion Cells

Science.gov (United States)

Ehrlich, Grant M.; Durand, Christopher

2005-01-01

Experimental materials made from mixtures of nickel and tin powders have shown promise for use as the negative electrodes of rechargeable lithium-ion electrochemical power cells. During charging (or discharging) of a lithium-ion cell, lithium ions are absorbed into (or desorbed from, respectively) the negative electrode, typically through an intercalation or alloying process. The negative electrodes (for this purpose, designated as anodes) in state-of-the-art Li-ion cells are made of graphite, in which intercalation occurs. Alternatively, the anodes can be made from metals, in which alloying can occur. For reasons having to do with the electrochemical potential of intercalated lithium, metallic anode materials (especially materials containing tin) are regarded as safer than graphite ones; in addition, such metallic anode materials have been investigated in the hope of obtaining reversible charge/discharge capacities greater than those of graphite anodes. However, until now, each of the tin-containing metallic anode formulations tested has been found to be inadequate in some respect.

Effects of Electrode Material on the Voltage of a Tree-Based Energy Generator.

Directory of Open Access Journals (Sweden)

Zhibin Hao

Full Text Available The voltage between a standing tree and its surrounding soil is regarded as an innovative renewable energy source. This source is expected to provide a new power generation system for the low-power electrical equipment used in forestry. However, the voltage is weak, which has caused great difficulty in application. Consequently, the development of a method to increase the voltage is a key issue that must be addressed in this area of applied research. As the front-end component for energy harvesting, a metal electrode has a material effect on the level and stability of the voltage obtained. This study aimed to preliminarily ascertain the rules and mechanisms that underlie the effects of electrode material on voltage. Electrodes of different materials were used to measure the tree-source voltage, and the data were employed in a comparative analysis. The results indicate that the conductivity of the metal electrode significantly affects the contact resistance of the electrode-soil and electrode-trunk contact surfaces, thereby influencing the voltage level. The metal reactivity of the electrode has no significant effect on the voltage. However, passivation of the electrode materials markedly reduces the voltage. Suitable electrode materials are demonstrated and recommended.

Sol-gel derived electrode materials for supercapacitor applications

Science.gov (United States)

Lin, Chuan

1998-12-01

Electrochemical capacitors have been receiving increasing interest in recent years for use in energy storage systems because of their high energy and power density and long cycle lifes. Possible applications of electrochemical capacitors include high power pulsed lasers, hybrid power system for electric vehicles, etc. In this dissertation, the preparation of electrode materials for use as electrochemical capacitors has been studied using the sol-gel process. The high surface area electrode materials explored in this work include a synthetic carbon xerogel for use in a double-layer capacitor, a cobalt oxide xerogel for use in a pseudocapacitor, and a carbon-ruthenium xerogel composite, which utilizes both double-layer and faradaic capacitances. The preparation conditions of these materials were investigated in detail to maximize the surface area and optimize the pore size so that more energy could be stored while minimizing mass transfer limitations. The microstructures of the materials were also correlated with their performance as electrochemical capacitors to improve their energy and power densities. Finally, an idealistic mathematical model, including both double-layer and faradaic processes, was developed and solved numerically. This model can be used to perform the parametric studies of an electrochemical capacitor so as to gain a better understanding of how the capacitor works and also how to improve cell operations and electrode materials design.

High Reversibility of “Soft” Electrode Materials in All-Solid-State Batteries

Energy Technology Data Exchange (ETDEWEB)

Sakuda, Atsushi, E-mail: a.sakuda@aist.go.jp; Takeuchi, Tomonari, E-mail: a.sakuda@aist.go.jp; Shikano, Masahiro; Sakaebe, Hikari; Kobayashi, Hironori [Department of Energy and Environment, Research Institute for Electrochemical Energy, National Institute of Advanced Industrial Science and Technology (AIST), Ikeda (Japan)

2016-05-10

All-solid-state batteries using inorganic solid electrolytes (SEs) are considered to be ideal batteries for electric vehicles and plug-in hybrid electric vehicles because they are potentially safer than conventional lithium-ion batteries (LIBs). In addition, all-solid-state batteries are expected to have long battery life owing to the inhibition of chemical side reactions because only lithium ions move through the typically used inorganic SEs. The development of high-energy density (more than 300 Wh kg{sup −1}) secondary batteries has been eagerly anticipated for years. The application of high-capacity electrode active materials is essential for fabricating such batteries. Recently, we proposed metal polysulfides as new electrode materials. These materials show higher conductivity and density than sulfur, which is advantageous for fabricating batteries with relatively higher energy density. Lithium niobium sulfides, such as Li{sub 3}NbS{sub 4}, have relatively high density, conductivity, and rate capability among metal polysulfide materials, and batteries with these materials have capacities high enough to potentially exceed the gravimetric-energy density of conventional LIBs. Favorable solid–solid contact between the electrode and electrolyte particles is a key factor for fabricating high performance all-solid-state batteries. Conventional oxide-based positive electrode materials tend to give rise to cracks during fabrication and/or charge–discharge processes. Here, we report all-solid-state cells using lithium niobium sulfide as a positive electrode material, where favorable solid–solid contact was established by using lithium sulfide electrode materials because of their high processability. Cracks were barely observed in the electrode particles in the all-solid-state cells before or after charging and discharging with a high capacity of approximately 400 mAh g{sup −1} suggesting that the lithium niobium sulfide electrode charged and discharged without

High Reversibility of “Soft” Electrode Materials in All-Solid-State Batteries

International Nuclear Information System (INIS)

Sakuda, Atsushi; Takeuchi, Tomonari; Shikano, Masahiro; Sakaebe, Hikari; Kobayashi, Hironori

2016-01-01

All-solid-state batteries using inorganic solid electrolytes (SEs) are considered to be ideal batteries for electric vehicles and plug-in hybrid electric vehicles because they are potentially safer than conventional lithium-ion batteries (LIBs). In addition, all-solid-state batteries are expected to have long battery life owing to the inhibition of chemical side reactions because only lithium ions move through the typically used inorganic SEs. The development of high-energy density (more than 300 Wh kg −1 ) secondary batteries has been eagerly anticipated for years. The application of high-capacity electrode active materials is essential for fabricating such batteries. Recently, we proposed metal polysulfides as new electrode materials. These materials show higher conductivity and density than sulfur, which is advantageous for fabricating batteries with relatively higher energy density. Lithium niobium sulfides, such as Li 3 NbS 4 , have relatively high density, conductivity, and rate capability among metal polysulfide materials, and batteries with these materials have capacities high enough to potentially exceed the gravimetric-energy density of conventional LIBs. Favorable solid–solid contact between the electrode and electrolyte particles is a key factor for fabricating high performance all-solid-state batteries. Conventional oxide-based positive electrode materials tend to give rise to cracks during fabrication and/or charge–discharge processes. Here, we report all-solid-state cells using lithium niobium sulfide as a positive electrode material, where favorable solid–solid contact was established by using lithium sulfide electrode materials because of their high processability. Cracks were barely observed in the electrode particles in the all-solid-state cells before or after charging and discharging with a high capacity of approximately 400 mAh g −1 suggesting that the lithium niobium sulfide electrode charged and discharged without experiencing

Towards Flexible Transparent Electrodes Based on Carbon and Metallic Materials

Directory of Open Access Journals (Sweden)

Minghui Luo

2017-01-01

Full Text Available Flexible transparent electrodes (FTEs with high stability and scalability are in high demand for the extremely widespread applications in flexible optoelectronic devices. Traditionally, thin films of indium thin oxide (ITO served the role of FTEs, but film brittleness and scarcity of materials limit its further application. This review provides a summary of recent advances in emerging transparent electrodes and related flexible devices (e.g., touch panels, organic light-emitting diodes, sensors, supercapacitors, and solar cells. Mainly focusing on the FTEs based on carbon nanomaterials (e.g., carbon nanotubes and graphene and metal materials (e.g., metal grid and metal nanowires, we discuss the fabrication techniques, the performance improvement, and the representative applications of these highly transparent and flexible electrodes. Finally, the challenges and prospects of flexible transparent electrodes will be summarized.

Graphene oxide - Polyvinyl alcohol nanocomposite based electrode material for supercapacitors

Science.gov (United States)

Pawar, Pranav Bhagwan; Shukla, Shobha; Saxena, Sumit

2016-07-01

Supercapacitors are high capacitive energy storage devices and find applications where rapid bursts of power are required. Thus materials offering high specific capacitance are of fundamental interest in development of these electrochemical devices. Graphene oxide based nanocomposites are mechanically robust and have interesting electronic properties. These form potential electrode materials efficient for charge storage in supercapacitors. In this perspective, we investigate low cost graphene oxide based nanocomposites as electrode material for supercapacitor. Nanocomposites of graphene oxide and polyvinyl alcohol were synthesized in solution phase by integrating graphene oxide as filler in polyvinyl alcohol matrix. Structural and optical characterizations suggest the formation of graphene oxide and polyvinyl alcohol nanocomposites. These nanocomposites were found to have high specific capacitance, were cyclable, ecofriendly and economical. Our studies suggest that nanocomposites prepared by adding 0.5% wt/wt of graphene oxide in polyvinyl alcohol can be used an efficient electrode material for supercapacitors.

Coaxial fiber supercapacitor using all-carbon material electrodes.

Science.gov (United States)

Le, Viet Thong; Kim, Heetae; Ghosh, Arunabha; Kim, Jaesu; Chang, Jian; Vu, Quoc An; Pham, Duy Tho; Lee, Ju-Hyuck; Kim, Sang-Woo; Lee, Young Hee

2013-07-23

We report a coaxial fiber supercapacitor, which consists of carbon microfiber bundles coated with multiwalled carbon nanotubes as a core electrode and carbon nanofiber paper as an outer electrode. The ratio of electrode volumes was determined by a half-cell test of each electrode. The capacitance reached 6.3 mF cm(-1) (86.8 mF cm(-2)) at a core electrode diameter of 230 μm and the measured energy density was 0.7 μWh cm(-1) (9.8 μWh cm(-2)) at a power density of 13.7 μW cm(-1) (189.4 μW cm(-2)), which were much higher than the previous reports. The change in the cyclic voltammetry characteristics was negligible at 180° bending, with excellent cycling performance. The high capacitance, high energy density, and power density of the coaxial fiber supercapacitor are attributed to not only high effective surface area due to its coaxial structure and bundle of the core electrode, but also all-carbon materials electrodes which have high conductivity. Our coaxial fiber supercapacitor can promote the development of textile electronics in near future.

Material for electrodes of low temperature plasma generators

Science.gov (United States)

Caplan, Malcolm; Vinogradov, Sergel Evge'evich; Ribin, Valeri Vasil'evich; Shekalov, Valentin Ivanovich; Rutberg, Philip Grigor'evich; Safronov, Alexi Anatol'evich

2008-12-09

Material for electrodes of low temperature plasma generators. The material contains a porous metal matrix impregnated with a material emitting electrons. The material uses a mixture of copper and iron powders as a porous metal matrix and a Group IIIB metal component such as Y.sub.2O.sub.3 is used as a material emitting electrons at, for example, the proportion of the components, mass %: iron: 3-30; Y.sub.2O.sub.3:0.05-1; copper: the remainder. Copper provides a high level of heat conduction and electric conductance, iron decreases intensity of copper evaporation in the process of plasma creation providing increased strength and lifetime, Y.sub.2O.sub.3 provides decreasing of electronic work function and stability of arc burning. The material can be used for producing the electrodes of low temperature AC plasma generators used for destruction of liquid organic wastes, medical wastes, and municipal wastes as well as for decontamination of low level radioactive waste, the destruction of chemical weapons, warfare toxic agents, etc.

A Viable Electrode Material for Use in Microbial Fuel Cells for Tropical Regions

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Felix Offei

2016-01-01

Full Text Available Electrode materials are critical for microbial fuel cells (MFC since they influence the construction and operational costs. This study introduces a simple and efficient electrode material in the form of palm kernel shell activated carbon (AC obtained in tropical regions. The novel introduction of this material is also targeted at introducing an inexpensive and durable electrode material, which can be produced in rural communities to improve the viability of MFCs. The maximum voltage and power density obtained (under 1000 Ω load using an H-shaped MFC with AC as both anode and cathode electrode material was 0.66 V and 1.74 W/m3, respectively. The power generated by AC was as high as 86% of the value obtained with the extensively used carbon paper. Scanning electron microscopy and Denaturing Gradient Gel Electrophoresis (DGGE analysis of AC anode biofilms confirmed that electrogenic bacteria were present on the electrode surface for substrate oxidation and the formation of nanowires.

Carbonaceous electrode materials for supercapacitors.

Science.gov (United States)

Hao, Long; Li, Xianglong; Zhi, Linjie

2013-07-26

Supercapacitors have been widely studied around the world in recent years, due to their excellent power density and long cycle life. As the most frequently used electrode materials for supercapacitors, carbonaceous materials attract more and more attention. However, their relatively low energy density still holds back the widespread application. Up to now, various strategies have been developed to figure out this problem. This research news summarizes the recent advances in improving the supercapacitor performance of carbonaceous materials, including the incorporation of heteroatoms and the pore size effect (subnanopores' contribution). In addition, a new class of carbonaceous materials, porous organic networks (PONs) has been managed into the supercapacitor field, which promises great potential in not only improving the supercapacitor performances, but also unraveling the related mechanisms. Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Sustainable Materials for Sustainable Energy Storage: Organic Na Electrodes

Science.gov (United States)

Oltean, Viorica-Alina; Renault, Stéven; Valvo, Mario; Brandell, Daniel

2016-01-01

In this review, we summarize research efforts to realize Na-based organic materials for novel battery chemistries. Na is a more abundant element than Li, thereby contributing to less costly materials with limited to no geopolitical constraints while organic electrode materials harvested from biomass resources provide the possibility of achieving renewable battery components with low environmental impact during processing and recycling. Together, this can form the basis for truly sustainable electrochemical energy storage. We explore the efforts made on electrode materials of organic salts, primarily carbonyl compounds but also Schiff bases, unsaturated compounds, nitroxides and polymers. Moreover, sodiated carbonaceous materials derived from biomasses and waste products are surveyed. As a conclusion to the review, some shortcomings of the currently investigated materials are highlighted together with the major limitations for future development in this field. Finally, routes to move forward in this direction are suggested. PMID:28773272

Fabrication of a three-electrode battery using hydrogen-storage materials

Science.gov (United States)

Roh, Chi-Woo; Seo, Jung-Yong; Moon, Hyung-Seok; Park, Hyun-Young; Nam, Na-Yun; Cho, Sung Min; Yoo, Pil J.; Chung, Chan-Hwa

2015-04-01

In this study, an energy storage device using a three-electrode battery is fabricated. The charging process takes place during electrolysis of the alkaline electrolyte where hydrogen is stored at the palladium bifunctional electrode. Upon discharging, power is generated by operating the alkaline fuel cell using hydrogen which is accumulated in the palladium hydride bifunctional electrode during the charging process. The bifunctional palladium electrode is prepared by electrodeposition using a hydrogen bubble template followed by a galvanic displacement reaction of platinum in order to functionalize the electrode to work not only as a hydrogen storage material but also as an anode in a fuel cell. This bifunctional electrode has a sufficiently high surface area and the platinum catalyst populates at the surface of electrode to operate the fuel cell. The charging and discharging performance of the three-electrode battery are characterized. In addition, the cycle stability is investigated.

A Local Region of Interest Imaging Method for Electrical Impedance Tomography with Internal Electrodes

Directory of Open Access Journals (Sweden)

Hyeuknam Kwon

2013-01-01

Full Text Available Electrical Impedance Tomography (EIT is a very attractive functional imaging method despite the low sensitivity and resolution. The use of internal electrodes with the conventional reconstruction algorithms was not enough to enhance image resolution and accuracy in the region of interest (ROI. We propose a local ROI imaging method with internal electrodes developed from careful analysis of the sensitivity matrix that is designed to reduce the sensitivity of the voxels outside the local region and optimize the sensitivity of the voxel inside the local region. We perform numerical simulations and physical measurements to demonstrate the localized EIT imaging method. In preliminary results with multiple objects we show the benefits of using an internal electrode and the improved resolution due to the local ROI image reconstruction method. The sensitivity is further increased by allowing the surface electrodes to be unevenly spaced with a higher density of surface electrodes near the ROI. Also, we analyse how much the image quality is improved using several performance parameters for comparison. While these have not yet been studied in depth, it convincingly shows an improvement in local sensitivity in images obtained with an internal electrode in comparison to a standard reconstruction method.

Microwave synthesis of electrode materials for lithium batteries

Indian Academy of Sciences (India)

A novel microwave method is described for the preparation of electrode materials required for lithium batteries. The method is simple, fast and carried out in most cases with the same starting material as in conventional methods. Good crystallinity has been noted and lower temperatures of reaction has been inferred in ...

Addition of internal electrodes is beneficial for focused bioimpedance measurements in the lung.

Science.gov (United States)

Orschulik, Jakob; Hochhausen, Nadine; Czaplik, Michael; Teichmann, Daniel; Leonhardt, Steffen; Walter, Marian

2018-03-29

Bioimpedance measurements such as bioimpedance spectroscopy (BIS) or electrical impedance tomography (EIT) are used in many biomedical applications. While BIS measures and analyzes the impedance in a frequency range at constant electrode positions, EIT aims to reconstruct images of the conductivity distribution from multiple measurements at different electrode positions. Our aim is to add spatial information to tetrapolar BIS measurements by using electrode positions that focus measurements on desired regions of interest. In this paper, we aim to investigate, whether internal electrodes that can be integrated into breathing or gastroesophageal tubes, can improve the local sensitivity of bioimpedance spectroscopy measurements. We present the results of a simulation study, in which we investigated more than 4 M different electrode configurations on their ability to monitor specific regions of interest (ROI) in the lung. Based on the sensitivity, which describes the impact of a conductivity change on the measured impedance, we define three main criteria which we use to evaluate our simulation results: the selectivity [Formula: see text], which describes the impact of a conductivity change inside the region of interest compared to a conductivity change outside the ROI; the homogeneity [Formula: see text], which describes the distribution of the sensitivity inside the ROI; and the absolute impedance contribution ratio [Formula: see text], which describes the contribution of the ROI to the measured impedance. Depending on the region of interest, electrode configurations using internal electrodes are between 9.8 % and 90 % better with respect to these criteria than configurations using external electrodes only. The combination of internal and external electrodes improves the focusing ability of tetrapolar impedance measurements on specific lung regions, which may be especially beneficial for lung monitoring in intensive care.

Oxide materials as positive electrodes of lithium-ion batteries

International Nuclear Information System (INIS)

Makhonina, Elena V; Pervov, Vladislav S; Dubasova, Valeriya S

2004-01-01

The published data on oxide materials as positive electrodes for lithium-ion batteries are described systematically. The mechanisms of structural changes in cathode materials occurring during the operation of lithium-ion batteries and the problems concerned with their selection are discussed. Modern trends in optimising cathode materials and lithium-ion batteries on the whole are considered.

Mixed bi-material electrodes based on LiMn2O4 and activated carbon for hybrid electrochemical energy storage devices

International Nuclear Information System (INIS)

Cericola, Dario; Novak, Petr; Wokaun, Alexander; Koetz, Ruediger

2011-01-01

Highlights: → Bi-material electrodes for electrochemical hybrid devices were characterized. → Bi-material electrodes have higher specific charge than capacitor electrodes. → Bi-material electrodes have better rate capability than battery electrodes. → Bi-material systems outperform batteries and capacitors in pulsed applications. - Abstract: The performance of mixed bi-material electrodes composed of the battery material, LiMn 2 O 4 , and the electrochemical capacitor material, activated carbon, for hybrid electrochemical energy storage devices is investigated by galvanostatic charge/discharge and pulsed discharge experiments. Both, a high and a low conductivity lithium-containing electrolyte are used. The specific charge of the bi-material electrode is the linear combination of the specific charges of LiMn 2 O 4 and activated carbon according to the electrode composition at low discharge rates. Thus, the specific charge of the bi-material electrode falls between the specific charge of the activated carbon electrode and the LiMn 2 O 4 battery electrode. The bi-material electrodes have better rate capability than the LiMn 2 O 4 battery electrode. For high current pulsed applications the bi-material electrodes typically outperform both the battery and the capacitor electrode.

Nanostructured manganese oxide thin films as electrode material for supercapacitors

Science.gov (United States)

Xia, Hui; Lai, Man On; Lu, Li

2011-01-01

Electrochemical capacitors, also called supercapacitors, are alternative energy storage devices, particularly for applications requiring high power densities. Recently, manganese oxides have been extensively evaluated as electrode materials for supercapacitors due to their low cost, environmental benignity, and promising supercapacitive performance. In order to maximize the utilization of manganese oxides as the electrode material for the supercapacitors and improve their supercapacitive performance, the nanostructured manganese oxides have therefore been developed. This paper reviews the synthesis of the nanostructured manganese oxide thin films by different methods and the supercapacitive performance of different nanostructures.

Crystallic silver amalgam – a novel electrode material

Czech Academy of Sciences Publication Activity Database

Daňhel, A.; Mansfeldová, Věra; Janda, Pavel; Vyskočil, V.; Barek, J.

2011-01-01

Roč. 136, č. 118 (2011), s. 36563662 ISSN 0003-2654 Institutional research plan: CEZ:AV0Z40400503 Keywords : crystallic silver amalgam * electrode materials * electrochemistry Subject RIV: CG - Electrochemistry Impact factor: 4.230, year: 2011

Electrode stabilizing materials

Science.gov (United States)

Amine, Khalil; Abouimrane, Ali; Moore, Jeffrey S.; Odom, Susan A.

2015-11-03

An electrolyte includes a polar aprotic solvent; an alkali metal salt; and an electrode stabilizing compound that is a monomer, which when polymerized forms an electrically conductive polymer. The electrode stabilizing compound is a thiophene, a imidazole, a anilines, a benzene, a azulene, a carbazole, or a thiol. Electrochemical devices may incorporate such electrolytes.

Compliant Electrode and Composite Material for Piezoelectric Wind and Mechanical Energy Conversions

Science.gov (United States)

Chen, Bin (Inventor)

2015-01-01

A thin film device for harvesting energy from wind. The thin film device includes one or more layers of a compliant piezoelectric material formed from a composite of a polymer and an inorganic material, such as a ceramic. Electrodes are disposed on a first side and a second side of the piezoelectric material. The electrodes are formed from a compliant material, such as carbon nanotubes or graphene. The thin film device exhibits improved resistance to structural fatigue upon application of large strains and repeated cyclic loadings.

Molybdate Based Ceramic Negative-Electrode Materials for Solid Oxide Cells

DEFF Research Database (Denmark)

Graves, Christopher R.; Reddy Sudireddy, Bhaskar; Mogensen, Mogens Bjerg

2010-01-01

Novel molybdate materials with varying Mo valence were synthesized as possible negative-electrode materials for solid oxide cells. The phase, stability, microstructure and electrical conductivity were characterized. The electrochemical activity for H2O and CO2 reduction and H2 and CO oxidation...... enhanced the electrocatalytic activity and electronic conductivity. The polarization resistances of the best molybdates were two orders of magnitude lower than that of donor-doped strontium titanates. Many of the molybdate materials were significantly activated by cathodic polarization, and they exhibited...... higher performance for cathodic (electrolysis) polarization than for anodic (fuel cell) polarization, which makes them especially interesting for use in electrolysis electrodes. ©2010 COPYRIGHT ECS - The Electrochemical Society...

Ir-Ni oxide as a promising material for nerve and brain stimulating electrodes

Directory of Open Access Journals (Sweden)

Joan Stilling

2014-09-01

Full Text Available Tremendous potential for successful medical device development lies in both electrical stimulation therapies and neuronal prosthetic devices, which can be utilized in an extensive number of neurological disorders. These technologies rely on the successful electrical stimulation of biological tissue (i.e. neurons through the use of electrodes. However, this technology faces the principal problem of poor stimulus selectivity due to the currently available electrode’s large size relative to its targeted population of neurons. Irreversible damage to both the stimulated tissue and electrode are limiting factors in miniaturization of this technology, as charge density increases with decreasing electrode size. In an attempt to find an equilibrium between these two opposing constraints (electrode size and charge density, the objective of this work was to develop a novel iridium-nickel oxide (Ir0.2-Ni0.8-oxide coating that could intrinsically offer high charge storage capacity. Thermal decomposition was used to fabricate titanium oxide, iridium oxide, nickel oxide, and bimetallic iridium-nickel oxide coatings on titanium electrode substrates. The Ir0.2-Ni0.8-oxide coating yielded the highest intrinsic (material property and extrinsic (material property + surface area charge storage capacity (CSC among the investigated materials, exceeding the performance of the current state-of-the-art neural stimulating electrode, Ir-oxide. This indicates that the Ir0.2-Ni0.8-oxide material is a promising alternative to currently used Ir-oxide, Pt, Au and carbon-based stimulating electrodes.

Nitrogen Doped Macroporous Carbon as Electrode Materials for High Capacity of Supercapacitor

Directory of Open Access Journals (Sweden)

Yudong Li

2017-01-01

Full Text Available Nitrogen doped carbon materials as electrodes of supercapacitors have attracted abundant attention. Herein, we demonstrated a method to synthesize N-doped macroporous carbon materials (NMC with continuous channels and large size pores carbonized from polyaniline using multiporous silica beads as sacrificial templates to act as electrode materials in supercapacitors. By the nice carbonized process, i.e., pre-carbonization at 400 °C and then pyrolysis at 700/800/900/1000 °C, NMC replicas with high BET specific surface areas exhibit excellent stability and recyclability as well as superb capacitance behavior (~413 F ⋅ g−1 in alkaline electrolyte. This research may provide a method to synthesize macroporous materials with continuous channels and hierarchical pores to enhance the infiltration and mass transfer not only used as electrode, but also as catalyst somewhere micro- or mesopores do not work well.

Enhanced control of electrochemical response in metallic materials in neural stimulation electrode applications

Energy Technology Data Exchange (ETDEWEB)

Watkins, K.G.; Steen, W.M.; Manna, I. [Univ. of Liverpool (United Kingdom)] [and others

1996-12-31

New means have been investigated for the production of electrode devices (stimulation electrodes) which could be implanted in the human body in order to control pain, activate paralysed limbs or provide electrode arrays for cochlear implants for the deaf or for the relief of tinitus. To achieve this ion implantation and laser materials processing techniques were employed. Ir was ion implanted in Ti-6Al-4V alloy and the surface subsequently enriched in the noble metal by dissolution in sulphuric acid. For laser materials processing techniques, investigation has been carried out on the laser cladding and laser alloying of Ir in Ti wire. A particular aim has been the determination of conditions required for the formation of a two phase Ir, Ir-rich, and Ti-rich microstructure which would enable subsequent removal of the non-noble phase to leave a highly porous noble metal with large real surface area and hence improved charge carrying capacity compared with conventional non porous electrodes. Evaluation of the materials produced has been carried out using repetitive cyclic voltammetry, amongst other techniques. For laser alloyed Ir on Ti wire, it has been found that differences in the melting point and density of the materials makes control of the cladding or alloying process difficult. Investigation of laser process parameters for the control of alloying and cladding in this system was carried out and a set of conditions for the successful production of two phase Ir-rich and Ti-rich components in a coating layer with strong metallurgical bonding to the Ti alloy substrate was derived. The laser processed material displays excellent potential for further development in providing stimulation electrodes with the current carrying capacity of Ir but in a form which is malleable and hence capable of formation into smaller electrodes with improved spatial resolution compared with presently employed electrodes.

Method of preparation of carbon materials for use as electrodes in rechargeable batteries

Science.gov (United States)

Doddapaneni, Narayan; Wang, James C. F.; Crocker, Robert W.; Ingersoll, David; Firsich, David W.

1999-01-01

A method of producing carbon materials for use as electrodes in rechargeable batteries. Electrodes prepared from these carbon materials exhibit intercalation efficiencies of .apprxeq.80% for lithium, low irreversible loss of lithium, long cycle life, are capable of sustaining a high rates of discharge and are cheap and easy to manufacture. The method comprises a novel two-step stabilization process in which polymeric precursor materials are stabilized by first heating in an inert atmosphere and subsequently heating in air. During the stabilization process, the polymeric precursor material can be agitated to reduce particle fusion and promote mass transfer of oxygen and water vapor. The stabilized, polymeric precursor materials can then be converted to a synthetic carbon, suitable for fabricating electrodes for use in rechargeable batteries, by heating to a high temperature in a flowing inert atmosphere.

NiO nanosheet assembles for supercapacitor electrode materials

Directory of Open Access Journals (Sweden)

Huanhao Xiao

2016-06-01

Full Text Available In this paper, large scale hierarchically assembled NiO nanosheets have been favorably fabricated through a facile hydrothermal route. The as-prepared NiO nanosheet assembles were characterized in detail by various analytical techniques. The results showed these nanosheets present the thickness of about 30 nm and the surface area is 116.9 m2 g−1. These NiO nanosheet assembles were used as the working electrode materials in electrochemical tests, which demonstrated a specific capacitance value of 81.67 F g−1 at the current density of 0.5 A g−1 and excellent long cycle-life stability with 78.5% of its discharge specific capacitance retention after 3000 cycles at the current density of 0.5 A g−1, revealing the as-synthesized NiO nanosheet assembles might be a promising electrode material for supercapacitor applications.

Optimization of Inactive Material Content in Lithium Iron Phosphate Electrodes for High Power Applications

International Nuclear Information System (INIS)

Ha, Seonbaek; Ramani, Vijay K.; Lu, Wenquan; Prakash, Jai

2016-01-01

The electrochemical performance of lithium iron phosphate (LiFePO 4 ) electrodes has been studied to find the optimum content of inactive materials (carbon black + polyvinylidene difluoride [PVDF] polymer binder) and to better understand electrode performance with variation in electrode composition. Trade-offs between inactive material content and electrochemical performance have been characterized in terms of electrical resistance, rate-capability, area-specific impedance (ASI), pulse-power characterization, and energy density calculations. The ASI and electrical conductivity were found to correlate well with ohmic polarization. The results showed that a 80:10:10 (active material: binder: carbon agents) electrode had a higher pulse-power density and energy density at rates above 1C as compared to 90:5:5, 86:7:7 and 70:15:15 formulations, while the 70:15:15 electrode had the highest electrical conductivity of 0.79 S cm −1 . A CB/PVDF ratio of ca. 1.22 was found to be the optimum formulation of inactive material when the LiFePO 4 composition was 80 wt%.

Polyaniline (PANi based electrode materials for energy storage and conversion

Directory of Open Access Journals (Sweden)

Huanhuan Wang

2016-09-01

Full Text Available Polyaniline (PANi as one kind of conducting polymers has been playing a great role in the energy storage and conversion devices besides carbonaceous materials and metallic compounds. Due to high specific capacitance, high flexibility and low cost, PANi has shown great potential in supercapacitor. It alone can be used in fabricating an electrode. However, the inferior stability of PANi limits its application. The combination of PANi and other active materials (carbon materials, metal compounds or other polymers can surpass these intrinsic disadvantages of PANi. This review summarizes the recent progress in PANi based composites for energy storage/conversion, like application in supercapacitors, rechargeable batteries, fuel cells and water hydrolysis. Besides, PANi derived nitrogen-doped carbon materials, which have been widely employed as carbon based electrodes/catalysts, are also involved in this review. PANi as a promising material for energy storage/conversion is deserved for intensive study and further development.

Study on Electrochemical Performance of Carbonnanotubes/Fey 04 Composite Electrode Material

Directory of Open Access Journals (Sweden)

WANG Fang--yong

2017-02-01

Full Text Available For single super capacitor materials，each material has its own unique advantages and defects. In this paper, the synthesis of complex multi walled carbon nanotubes with Fe304 nanoparticles by simple hydrothermal method. Composite performance for Fe3 OQ nanoparticles adsorbed on carbon nano tube wall composed of reticular structure morphology. Synergy of two component，provides the binary nanometer compound larger specific capacity， excellent properties and good cycle stability. The experimental results proved that the improvement effects of CNT carbon materials on the electrochemical properties of pseudocapacitive electrode material，and CNT/Fe3 OQ nano- composites applied to supercapacitor electrode material.

High capacity electrode materials for batteries and process for their manufacture

Science.gov (United States)

Johnson, Christopher S.; Xiong, Hui; Rajh, Tijana; Shevchenko, Elena; Tepavcevic, Sanja

2018-04-03

The present invention provides a nanostructured metal oxide material for use as a component of an electrode in a lithium-ion or sodium-ion battery. The material comprises a nanostructured titanium oxide or vanadium oxide film on a metal foil substrate, produced by depositing or forming a nanostructured titanium dioxide or vanadium oxide material on the substrate, and then charging and discharging the material in an electrochemical cell from a high voltage in the range of about 2.8 to 3.8 V, to a low voltage in the range of about 0.8 to 1.4 V over a period of about 1/30 of an hour or less. Lithium-ion and sodium-ion electrochemical cells comprising electrodes formed from the nanostructured metal oxide materials, as well as batteries formed from the cells, also are provided.

Functional Biomass Carbons with Hierarchical Porous Structure for Supercapacitor Electrode Materials

International Nuclear Information System (INIS)

Chen, Hao; Liu, Duo; Shen, Zhehong; Bao, Binfu; Zhao, Shuyan; Wu, Limin

2015-01-01

Highlights: • We successfully prepared bamboo-derived porous carbon with B and N co-doping. • This novel carbon exhibits significantly enhanced specific capacitance and energy density. • The highest specific capacitance exceeds those of most similar carbon materials. • Asymmetric supercapacitor based on this carbon shows satisfactory capacitive performance. - Abstract: This paper presents nitrogen and boron co-doped KOH-activated bamboo-derived carbon as a porous biomass carbon with utility as a supercapacitor electrode material. Owing to the high electrochemical activity promoted by the hierarchical porous structure and further endowed by boron and nitrogen co-doping, electrodes based on the as-obtained material exhibit significantly enhanced specific capacitance and energy density relative to those based on most similar materials. An asymmetric supercapacitor based on this novel carbon material demonstrated satisfactory energy density and electrochemical cycling stability.

Recent Development of Advanced Electrode Materials by Atomic Layer Deposition for Electrochemical Energy Storage.

Science.gov (United States)

Guan, Cao; Wang, John

2016-10-01

Electrode materials play a decisive role in almost all electrochemical energy storage devices, determining their overall performance. Proper selection, design and fabrication of electrode materials have thus been regarded as one of the most critical steps in achieving high electrochemical energy storage performance. As an advanced nanotechnology for thin films and surfaces with conformal interfacial features and well controllable deposition thickness, atomic layer deposition (ALD) has been successfully developed for deposition and surface modification of electrode materials, where there are considerable issues of interfacial and surface chemistry at atomic and nanometer scale. In addition, ALD has shown great potential in construction of novel nanostructured active materials that otherwise can be hardly obtained by other processing techniques, such as those solution-based processing and chemical vapor deposition (CVD) techniques. This review focuses on the recent development of ALD for the design and delivery of advanced electrode materials in electrochemical energy storage devices, where typical examples will be highlighted and analyzed, and the merits and challenges of ALD for applications in energy storage will also be discussed.

Gallium Nitride Crystals: Novel Supercapacitor Electrode Materials.

Science.gov (United States)

Wang, Shouzhi; Zhang, Lei; Sun, Changlong; Shao, Yongliang; Wu, Yongzhong; Lv, Jiaxin; Hao, Xiaopeng

2016-05-01

A type of single-crystal gallium nitride mesoporous membrane is fabricated and its supercapacitor properties are demonstrated for the first time. The supercapacitors exhibit high-rate capability, stable cycling life at high rates, and ultrahigh power density. This study may expand the range of crystals as high-performance electrode materials in the field of energy storage. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Plasma-Assisted Synthesis and Surface Modification of Electrode Materials for Renewable Energy.

Science.gov (United States)

Dou, Shuo; Tao, Li; Wang, Ruilun; El Hankari, Samir; Chen, Ru; Wang, Shuangyin

2018-02-14

Renewable energy technology has been considered as a "MUST" option to lower the use of fossil fuels for industry and daily life. Designing critical and sophisticated materials is of great importance in order to realize high-performance energy technology. Typically, efficient synthesis and soft surface modification of nanomaterials are important for energy technology. Therefore, there are increasing demands on the rational design of efficient electrocatalysts or electrode materials, which are the key for scalable and practical electrochemical energy devices. Nevertheless, the development of versatile and cheap strategies is one of the main challenges to achieve the aforementioned goals. Accordingly, plasma technology has recently appeared as an extremely promising alternative for the synthesis and surface modification of nanomaterials for electrochemical devices. Here, the recent progress on the development of nonthermal plasma technology is highlighted for the synthesis and surface modification of advanced electrode materials for renewable energy technology including electrocatalysts for fuel cells, water splitting, metal-air batteries, and electrode materials for batteries and supercapacitors, etc. © 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

The impact of electrode materials on 1/f noise in piezoelectric AlN contour mode resonators

Science.gov (United States)

Kim, Hoe Joon; Jung, Soon In; Segovia-Fernandez, Jeronimo; Piazza, Gianluca

2018-05-01

This paper presents a detailed analysis on the impact of electrode materials and dimensions on flicker frequency (1/f) noise in piezoelectric aluminum nitride (AlN) contour mode resonators (CMRs). Flicker frequency noise is a fundamental noise mechanism present in any vibrating mechanical structure, whose sources are not generally well understood. 1 GHz AlN CMRs with three different top electrode materials (Al, Au, and Pt) along with various electrode lengths and widths are fabricated to control the overall damping acting on the device. Specifically, the use of different electrode materials allows control of thermoelastic damping (TED), which is the dominant damping mechanism for high frequency AlN CMRs and largely depends on the thermal properties (i.e. thermal diffusivities and expansion coefficients) of the metal electrode rather than the piezoelectric film. We have measured Q and 1/f noise of 68 resonators and the results show that 1/f noise decreases with increasing Q, with a power law dependence that is about 1/Q4. Interestingly, the noise level also depends on the type of electrode materials. Devices with Pt top electrode demonstrate the best noise performance. Our results help unveiling some of the sources of 1/f noise in these resonators, and indicate that a careful selection of the electrode material and dimensions could reduce 1/f noise not only in AlN-CMRs, but also in various classes of resonators, and thus enable ultra-low noise mechanical resonators for sensing and radio frequency applications.

Synchrotron x-ray diffraction studies of the structural properties of electrode materials in operating battery cells

International Nuclear Information System (INIS)

Thurston, T.R.; Jisrawi, N.M.; Mukerjee, S.; Yang, X.Q.; McBreen, J.; Daroux, M.L.; Xing, X.K.

1996-01-01

Hard x rays from a synchrotron source were utilized in diffraction experiments which probed the bulk of electrode materials while they were operating in situ in battery cells. Two technologically relevant electrode materials were examined; an AB 2 -type anode in a nickel endash metal endash hydride cell and a LiMn 2 O 4 cathode in a Li-ion open-quote open-quote rocking chair close-quote close-quote cell. Structural features such as lattice expansions and contractions, phase transitions, and the formation of multiple phases were easily observed as either hydrogen or lithium was electrochemically intercalated in and out of the electrode materials. The relevance of this technique for future studies of battery electrode materials is discussed. copyright 1996 American Institute of Physics

Method of preparing an electrode material of lithium-aluminum alloy

Science.gov (United States)

Settle, Jack L.; Myles, Kevin M.; Battles, James E.

1976-01-01

A solid compact having a uniform alloy composition of lithium and aluminum is prepared as a negative electrode for an electrochemical cell. Lithium losses during preparation are minimized by dissolving aluminum within a lithium-rich melt at temperatures near the liquidus temperatures. The desired alloy composition is then solidified and fragmented. The fragments are homogenized to a uniform composition by annealing at a temperature near the solidus temperature. After comminuting to fine particles, the alloy material can be blended with powdered electrolyte and pressed into a solid compact having the desired electrode shape. In the preparation of some electrodes, an electrically conductive metal mesh is embedded into the compact as a current collector.

Influence of various Activated Carbon based Electrode Materials in the Performance of Super Capacitor

Science.gov (United States)

Ajay, K. M.; Dinesh, M. N.

2018-02-01

Various activated carbon based electrode materials with different surface areas was prepared on stainless steel based refillable super capacitor model using spin coating. Bio Synthesized Activated Carbon (BSAC), Activated Carbon (AC) and Graphite powder are chosen as electrode materials in this paper. Electrode materials prepared using binder solution which is 6% by wt. polyvinylidene difluoride, 94% by wt. dimethyl fluoride. 3M concentrated KOH solution is used as aqueous electrolyte with PVDF thin film as separator. It is tested for electrochemical characterizations and material characterizations. It is observed that the Specific capacitance of Graphite, Biosynthesized active carbon and Commercially available activated carbon are 16.1F g-1, 53.4F g-1 and 107.6F g-1 respectively at 5mV s-1 scan rate.

Electrostatic Spectrograph with a Wide Range of Simultaneously Recorded Energies Composed of Two Coaxial Electrodes with Closed End Faces and a Discrete Combined External Electrode

Science.gov (United States)

Fishkova, T. Ya.

2018-01-01

An optimal set of geometric and electrical parameters of a high-aperture electrostatic charged-particle spectrograph with a range of simultaneously recorded energies of E/ E min = 1-50 has been found by computer simulation, which is especially important for the energy analysis of charged particles during fast processes in various materials. The spectrograph consists of two coaxial electrodes with end faces closed by flat electrodes. The external electrode with a conical-cylindrical form is cut into parts with potentials that increase linearly, except for the last cylindrical part, which is electrically connected to the rear end electrode. The internal cylindrical electrode and the front end electrode are grounded. In the entire energy range, the system is sharply focused on the internal cylindrical electrode, which provides an energy resolution of no worse than 3 × 10-3.

Nanostructured pseudocapacitive materials decorated 3D graphene foam electrodes for next generation supercapacitors.

Science.gov (United States)

Patil, Umakant; Lee, Su Chan; Kulkarni, Sachin; Sohn, Ji Soo; Nam, Min Sik; Han, Suhyun; Jun, Seong Chan

2015-04-28

Nowadays, advancement in performance of proficient multifarious electrode materials lies conclusively at the core of research concerning energy storage devices. To accomplish superior capacitance performance the requirements of high capacity, better cyclic stability and good rate capability can be expected from integration of electrochemical double layer capacitor based carbonaceous materials (high power density) and pseudocapacitive based metal hydroxides/oxides or conducting polymers (high energy density). The envisioned three dimensional (3D) graphene foams are predominantly advantageous to extend potential applicability by offering a large active surface area and a highly conductive continuous porous network for fast charge transfer with decoration of nanosized pseudocapacitive materials. In this article, we review the latest methodologies and performance evaluation for several 3D graphene based metal oxides/hydroxides and conducting polymer electrodes with improved electrochemical properties for next-generation supercapacitors. The most recent research advancements of our and other groups in the field of 3D graphene based electrode materials for supercapacitors are discussed. To assess the studied materials fully, a careful interpretation and rigorous scrutiny of their electrochemical characteristics is essential. Auspiciously, both nano-structuration as well as confinement of metal hydroxides/oxides and conducting polymers onto a conducting porous 3D graphene matrix play a great role in improving the performance of electrodes mainly due to: (i) active material access over large surface area with fast charge transportation; (ii) synergetic effect of electric double layer and pseudocapacitive based charge storing.

High performance lithium insertion negative electrode materials for electrochemical devices

Energy Technology Data Exchange (ETDEWEB)

Channu, V.S. Reddy, E-mail: chinares02@gmail.com [SMC Corporation, College Station, TX 77845 (United States); Rambabu, B. [Solid State Ionics and Surface Sciences Lab, Department of Physics, Southern University and A& M College, Baton Rouge, LA 70813 (United States); Kumari, Kusum [Department of Physics, National Institute of Technology, Warangal (India); Kalluru, Rajmohan R. [The University of Southern Mississippi, College of Science and Technology, 730 E Beach Blvd, Long Beach, MS 39560 (United States); Holze, Rudolf [Institut für Chemie, AG Elektrochemie, Technische Universität Chemnitz, D-09107 Chemnitz (Germany)

2016-11-30

Highlights: • LiCrTiO{sub 4} nanostructures were synthesized for electrochemical applications by soft chemical synthesis followed by annealing. • The presence of Cr and Ti elements are confirmed from the EDS spectrum. • Oxalic acid assisted LiCrTiO{sub 4} electrode shows higher specific capacity (mAh/g). - Abstract: Spinel LiCrTiO{sub 4} oxides to be used as electrode materials for a lithium ion battery and an asymmetric supercapacitor were synthesized using a soft-chemical method with and without chelating agents followed by calcination at 700 °C for 10 h. Structural and morphological properties were studied with powder X-ray diffraction, scanning electron and transmission electron microscopy. Particles of 50–10 nm in size are observed in the microscopic images. The presence of Cr and Ti is confirmed from the EDS spectrum. Electrochemical properties of LiCrTiO{sub 4} electrode were examined in a lithium ion battery. The electrode prepared with oxalic acid-assisted LiCrTiO{sub 4} shows higher specific capacity.This LiCrTiO{sub 4} is also used as anode material for an asymmetric hybrid supercapacitor. The cell exhibits a specific capacity of 65 mAh/g at 1 mA/cm{sup 2}. The specific capacity decreases with increasing current densities.

The impact of electrode materials on 1/f noise in piezoelectric AlN contour mode resonators

Directory of Open Access Journals (Sweden)

Hoe Joon Kim

2018-05-01

Full Text Available This paper presents a detailed analysis on the impact of electrode materials and dimensions on flicker frequency (1/f noise in piezoelectric aluminum nitride (AlN contour mode resonators (CMRs. Flicker frequency noise is a fundamental noise mechanism present in any vibrating mechanical structure, whose sources are not generally well understood. 1 GHz AlN CMRs with three different top electrode materials (Al, Au, and Pt along with various electrode lengths and widths are fabricated to control the overall damping acting on the device. Specifically, the use of different electrode materials allows control of thermoelastic damping (TED, which is the dominant damping mechanism for high frequency AlN CMRs and largely depends on the thermal properties (i.e. thermal diffusivities and expansion coefficients of the metal electrode rather than the piezoelectric film. We have measured Q and 1/f noise of 68 resonators and the results show that 1/f noise decreases with increasing Q, with a power law dependence that is about 1/Q4. Interestingly, the noise level also depends on the type of electrode materials. Devices with Pt top electrode demonstrate the best noise performance. Our results help unveiling some of the sources of 1/f noise in these resonators, and indicate that a careful selection of the electrode material and dimensions could reduce 1/f noise not only in AlN-CMRs, but also in various classes of resonators, and thus enable ultra-low noise mechanical resonators for sensing and radio frequency applications.

Two-dimensional Cu2Si sheet: a promising electrode material for nanoscale electronics

Science.gov (United States)

Meng Yam, Kah; Guo, Na; Zhang, Chun

2018-06-01

Building electronic devices on top of two-dimensional (2D) materials has recently become one of most interesting topics in nanoelectronics. Finding high-performance 2D electrode materials is one central issue in 2D nanoelectronics. In the current study, based on first-principles calculations, we compare the electronic and transport properties of two nanoscale devices. One device consists of two single-atom-thick planar Cu2Si electrodes, and a nickel phthalocyanine (NiPc) molecule in the middle. The other device is made of often-used graphene electrodes and a NiPc molecule. Planer Cu2Si is a new type of 2D material that was recently predicted to exist and be stable under room temperature [11]. We found that at low bias voltages, the electric current through the Cu2Si–NiPc–Cu2Si junction is about three orders higher than that through graphene–NiPc–graphene. Detailed analysis shows that the surprisingly high conductivity of Cu2Si–NiPc–Cu2Si originates from the mixing of the Cu2Si state near Fermi energy and the highest occupied molecular orbital of NiPc. These results suggest that 2D Cu2Si may be an excellent candidate for electrode materials for future nanoscale devices.

Materials Science of Electrodes and Interfaces for High-Performance Organic Photovoltaics

Energy Technology Data Exchange (ETDEWEB)

Marks, Tobin [Northwestern Univ., Evanston, IL (United States)

2016-11-18

The science of organic photovoltaic (OPV) cells has made dramatic advances over the past three years with power conversion efficiencies (PCEs) now reaching ~12%. The upper PCE limit of light-to-electrical power conversion for single-junction OPVs as predicted by theory is ~23%. With further basic research, the vision of such devices, composed of non-toxic, earth-abundant, readily easily processed materials replacing/supplementing current-generation inorganic solar cells may become a reality. Organic cells offer potentially low-cost, roll-to-roll manufacturable, and durable solar power for diverse in-door and out-door applications. Importantly, further gains in efficiency and durability, to that competitive with inorganic PVs, will require fundamental, understanding-based advances in transparent electrode and interfacial materials science and engineering. This team-science research effort brought together an experienced and highly collaborative interdisciplinary group with expertise in hard and soft matter materials chemistry, materials electronic structure theory, solar cell fabrication and characterization, microstructure characterization, and low temperature materials processing. We addressed in unconventional ways critical electrode-interfacial issues underlying OPV performance -- controlling band offsets between transparent electrodes and organic active-materials, addressing current loss/leakage phenomena at interfaces, and new techniques in cost-effective low temperature and large area cell fabrication. The research foci were: 1) Theory-guided design and synthesis of advanced crystalline and amorphous transparent conducting oxide (TCO) layers which test our basic understanding of TCO structure-transport property relationships, and have high conductivity, transparency, and tunable work functions but without (or minimizing) the dependence on indium. 2) Development of theory-based understanding of optimum configurations for the interfaces between oxide electrodes

The progress of the electrode materials development for lithium ion battery

International Nuclear Information System (INIS)

Kang Kai; Dai Shouhui; Wan Yuhua

2001-01-01

The structure and the charge-discharge principle of Li-ion battery are briefly discussed; the progress of electrode materials for Li-ion battery is reviewed in detail. Graphite has found wide applications in commercial Li-ion batteries, however, the hard carbon, especially the carbon with hydrogen is the most promising anode material for Li-ion battery owing to its high capacity, which has now become hot spot of investigation. Following the LiCoO 2 , LiMn 2 O 4 spinel compound becomes the most powerful contestant. On the basis of the authors' results, the synthesis methods of LiMn 2 O 4 and its characterizations are compared. Moreover, the structural properties of intercalation electrode materials that are related to the rechargeable capacity and stability during cycling of lithium ions are also discussed

Preparation of Reduced Graphene Oxides as Electrode Materials for Supercapacitors

KAUST Repository

Bai, Yaocai

2012-01-01

Reduced graphene oxide as outstanding candidate electrode material for supercapacitor has been investigated. This thesis includes two topics. One is that three kinds of reduced graphene oxides were prepared by hydrothermal reduction under different

LDHs as electrode materials for electrochemical detection and energy storage: supercapacitor, battery and (bio)-sensor.

Science.gov (United States)

Mousty, Christine; Leroux, Fabrice

2012-11-01

From an exhaustive overview based on applicative academic literature and patent domain, the relevance of Layered Double Hydroxide (LDHs) as electrode materials for electrochemical detection of organic molecules having environmental or health impact and energy storage is evaluated. Specifically the focus is driven on their application as supercapacitor, alkaline or lithium battery and (bio)-sensor. Inherent to the high versatility of their chemical composition, charge density, anion exchange capability, LDH-based materials are extensively studied and their performances for such applications are reported. Indeed the analytical characteristics (sensitivity and detection limit) of LDH-based electrodes are scrutinized, and their specific capacity or capacitance as electrode battery or supercapacitor materials, are detailed.

Layered double hydroxide materials coated carbon electrode: New challenge to future electrochemical power devices

International Nuclear Information System (INIS)

Djebbi, Mohamed Amine; Braiek, Mohamed; Namour, Philippe; Ben Haj Amara, Abdesslem; Jaffrezic-Renault, Nicole

2016-01-01

Highlights: • MgAl and ZnAl LDH nanosheets were chemically synthesized and deposited over carbon electrode materials. • Catalytic performance of both LDHs was investigated for Fe(II) reduction reaction. • Satisfactory results have been achieved with the MgAl LDH material. • MgAl and ZnAl LDH modified carbon felt were applied in MFC as an efficient anode catalyst. • The LDH-modified anode significantly increased power performance of MFC. - Abstract: Layered double hydroxides (LDHs) have been widely used in the past years due to their unique physicochemical properties and promising applications in electroanalytical chemistry. The present paper is going to focus exclusively on magnesium-aluminum and zinc-aluminum layered double hydroxides (MgAl & ZnAl LDHs) in order to investigate the property and structure of active cation sites located within the layer structure. The MgAl and ZnAl LDH nanosheets were prepared by the constant pH co-precipitation method and uniformly supported on carbon-based electrode materials to fabricate an LDH electrode. Characterization by powder x-ray diffraction, Fourier transform infrared spectroscopy, scanning electron microscopy and transmission electron microscopy revealed the LDH form and well-crystallized materials. Wetting surface properties (hydrophilicity and hydrophobicity) of both prepared LDHs were recorded by contact angle measurement show hydrophilic character and basic property. The electrochemical performance of these hybrid materials was investigated by mainly cyclic voltammetry, electrochemical impedance spectroscopy and chronoamperometry techniques to identify the oxidation/reduction processes at the electrode/electrolyte interface and the effect of the divalent metal cations in total reactivity. The hierarchy of the modified electrode proves that the electronic conductivity of the bulk material is considerably dependent on the divalent cation and affects the limiting parameter of the overall redox process. However

Layered double hydroxide materials coated carbon electrode: New challenge to future electrochemical power devices

Energy Technology Data Exchange (ETDEWEB)

Djebbi, Mohamed Amine, E-mail: mohamed.djebbi@etu.univ-lyon1.fr [Institut des Sciences Analytiques UMR CNRS 5280, Université Claude Bernard-Lyon 1, 5 rue de la Doua, 69100 Villeurbanne (France); Laboratoire de Physique des Matériaux Lamellaires et Nano-Matériaux Hybrides, Faculté des Sciences de Bizerte, Université de Carthage, 7021 Bizerte (Tunisia); Braiek, Mohamed [Institut des Sciences Analytiques UMR CNRS 5280, Université Claude Bernard-Lyon 1, 5 rue de la Doua, 69100 Villeurbanne (France); Namour, Philippe [Institut des Sciences Analytiques UMR CNRS 5280, Université Claude Bernard-Lyon 1, 5 rue de la Doua, 69100 Villeurbanne (France); Irstea, 5 rue de la Doua, 69100 Villeurbanne (France); Ben Haj Amara, Abdesslem [Laboratoire de Physique des Matériaux Lamellaires et Nano-Matériaux Hybrides, Faculté des Sciences de Bizerte, Université de Carthage, 7021 Bizerte (Tunisia); Jaffrezic-Renault, Nicole [Institut des Sciences Analytiques UMR CNRS 5280, Université Claude Bernard-Lyon 1, 5 rue de la Doua, 69100 Villeurbanne (France)

2016-11-15

Highlights: • MgAl and ZnAl LDH nanosheets were chemically synthesized and deposited over carbon electrode materials. • Catalytic performance of both LDHs was investigated for Fe(II) reduction reaction. • Satisfactory results have been achieved with the MgAl LDH material. • MgAl and ZnAl LDH modified carbon felt were applied in MFC as an efficient anode catalyst. • The LDH-modified anode significantly increased power performance of MFC. - Abstract: Layered double hydroxides (LDHs) have been widely used in the past years due to their unique physicochemical properties and promising applications in electroanalytical chemistry. The present paper is going to focus exclusively on magnesium-aluminum and zinc-aluminum layered double hydroxides (MgAl & ZnAl LDHs) in order to investigate the property and structure of active cation sites located within the layer structure. The MgAl and ZnAl LDH nanosheets were prepared by the constant pH co-precipitation method and uniformly supported on carbon-based electrode materials to fabricate an LDH electrode. Characterization by powder x-ray diffraction, Fourier transform infrared spectroscopy, scanning electron microscopy and transmission electron microscopy revealed the LDH form and well-crystallized materials. Wetting surface properties (hydrophilicity and hydrophobicity) of both prepared LDHs were recorded by contact angle measurement show hydrophilic character and basic property. The electrochemical performance of these hybrid materials was investigated by mainly cyclic voltammetry, electrochemical impedance spectroscopy and chronoamperometry techniques to identify the oxidation/reduction processes at the electrode/electrolyte interface and the effect of the divalent metal cations in total reactivity. The hierarchy of the modified electrode proves that the electronic conductivity of the bulk material is considerably dependent on the divalent cation and affects the limiting parameter of the overall redox process. However

A viable electrode material for use in microbial fuel cells for tropical regions

DEFF Research Database (Denmark)

Offei, Felix; Thygesen, Anders; Mensah, Moses

2016-01-01

of this material is also targeted at introducing an inexpensive and durable electrode material, which can be produced in rural communities to improve the viability of MFCs. The maximum voltage and power density obtained (under 1000 Ω load) using an H-shaped MFC with AC as both anode and cathode electrode material...... was 0.66 V and 1.74 W/m3, respectively. The power generated by AC was as high as 86% of the value obtained with the extensively used carbon paper. Scanning electron microscopy and Denaturing Gradient Gel Electrophoresis (DGGE) analysis of AC anode biofilms confirmed that electrogenic bacteria were...

Electrode materials for hydrobromic acid electrolysis in Texas Instruments' solar chemical converter

Energy Technology Data Exchange (ETDEWEB)

Luttmer, J.D.; Konrad, D.; Trachtenberg, I.

1985-05-01

Texas Instruments has developed a solar chemical converter (SCC) which converts solar energy into chemical energy via the electrolysis of hydrobromic acid. Various materials were evaluated as anodes and cathodes for the electrolysis of the acid. Emphasis was placed on obtaining low overvoltage electrodes with good long-term stability. Sputtered platinum-iridium thin films were identified as the best choice as the cathode material, and sputtered iridium and iridium oxide thin films were identified as the best choice as anode materials. Electrochemical measurements indicate that low overvoltage losses are encountered on these materials at operating current densitities in the SCC. Accelerated corrosion tests of the materials predict acceptable electrode stability for 20 years in an environment representative of onthe-roof service.

Amperometric Detection in Microchip Electrophoresis Devices: Effect of Electrode Material and Alignment on Analytical Performance

Science.gov (United States)

Fischer, David J.; Hulvey, Matthew K.; Regel, Anne R.; Lunte, Susan M.

2012-01-01

The fabrication and evaluation of different electrode materials and electrode alignments for microchip electrophoresis with electrochemical (EC) detection is described. The influences of electrode material, both metal and carbon-based, on sensitivity and limits of detection (LOD) were examined. In addition, the effects of working electrode alignment on analytical performance (in terms of peak shape, resolution, sensitivity, and LOD) were directly compared. Using dopamine (DA), norepinephrine (NE), and catechol (CAT) as test analytes, it was found that pyrolyzed photoresist electrodes with end-channel alignment yielded the lowest limit of detection (35 nM for DA). In addition to being easier to implement, end-channel alignment also offered better analytical performance than off-channel alignment for the detection of all three analytes. In-channel electrode alignment resulted in a 3.6-fold reduction in peak skew and reduced peak tailing by a factor of 2.1 for catechol in comparison to end-channel alignment. PMID:19802847

Improved Internal Reference Oxygen Sensors Using Composite Oxides as Electrodes

DEFF Research Database (Denmark)

Hu, Qiang

The thesis describes the research on and development of an internal reference oxygen sensor (IROS). The IROS is potentiometric and uses the equilibrium pO2of the binary mixture of Ni/NiO as the reference pO2. The sensing electrode of the IROS are made from metallic Pt or the composite of (La0.75S...... the application of IROSes are provided. Based on the concepts and fundamentals of the IROS, internal reference sensors that detect other gas species such as hydrogen, chlorine and bromine may be developed.......The thesis describes the research on and development of an internal reference oxygen sensor (IROS). The IROS is potentiometric and uses the equilibrium pO2of the binary mixture of Ni/NiO as the reference pO2. The sensing electrode of the IROS are made from metallic Pt or the composite of (La0.75Sr0...... from 8YSZ is evaluated quantitatively and figures that may be used to design the depletion period of an IROS due to the electronic leak of 8YSZ are provided. One dimensional numerical simulations are performed to study the variation in cell voltage during the process of gas mixing, and the asymmetric...

Alternate electrode materials for the SP100 reactor

International Nuclear Information System (INIS)

Randich, E.

1992-05-01

This work was performed in response to a request by the Astro-Space Division of the General Electric Co. to develop alternate electrodes materials for the electrodes of the PD2 modules to be used in the SP100 thermoelectric power conversion system. Initially, the project consisted of four tasks: (1) development of a ZrB 2 (C) CVD coating on SiMo substrates, (2) development of a ZrB 2 (C) CVD coating on SiGe substrates, (3) development of CVI W for porous graphite electrodes, and (4) technology transfer of pertinent developed processes. The project evolved initially into developing only ZrB 2 coatings on SiGe and graphite substrates, and later into developing ZrB 2 coatings only on graphite substrates. Several sizes of graphite and pyrolytic carbon-coated graphite substrates were coated with ZrB 2 during the project. For budgetary reasons, the project was terminated after half the allotted time had passed. Apart from the production of coated specimens for evaluation, the major accomplishment of the project was the development of the CVD processing to produce the desired coatings

Synergetic Hybrid Aerogels of Vanadia and Graphene as Electrode Materials of Supercapacitors

Directory of Open Access Journals (Sweden)

Xuewei Fu

2016-08-01

Full Text Available The performance of synergetic hybrid aerogel materials of vanadia and graphene as electrode materials in supercapacitors was evaluated. The hybrid materials were synthesized by two methods. In Method I, premade graphene oxide (GO hydrogel was first chemically reduced by L-ascorbic acid and then soaked in vanadium triisopropoxide solution to obtain V2O5 gel in the pores of the reduced graphene oxide (rGO hydrogel. The gel was supercritically dried to obtain the hybrid aerogel. In Method II, vanadium triisopropoxide was hydrolyzed from a solution in water with GO particles uniformly dispersed to obtain the hybrid gel. The hybrid aerogel was obtained by supercritical drying of the gel followed by thermal reduction of GO. The electrode materials were prepared by mixing 80 wt % hybrid aerogel with 10 wt % carbon black and 10 wt % polyvinylidene fluoride. The hybrid materials in Method II showed higher capacitance due to better interactions between vanadia and graphene oxide particles and more uniform vanadia particle distribution.

EDM Electrode for Internal Grooves

Science.gov (United States)

Ramani, V.; Werner, A.

1985-01-01

Electroerosive process inexpensive alternative to broaching. Hollow brass electrodes, soldered at one end to stainless-steel holding ring, held in grooves in mandrel. These electrodes used to machine grooves electrically in stainless-steel tube three-eights inch (9.5 millimeters) in diameter. Tool used on tubes already in place in equipment.

Emerging Prototype Sodium-Ion Full Cells with Nanostructured Electrode Materials.

Science.gov (United States)

Ren, Wenhao; Zhu, Zixuan; An, Qinyou; Mai, Liqiang

2017-06-01

Due to steadily increasing energy consumption, the demand of renewable energy sources is more urgent than ever. Sodium-ion batteries (SIBs) have emerged as a cost-effective alternative because of the earth abundance of Na resources and their competitive electrochemical behaviors. Before practical application, it is essential to establish a bridge between the sodium half-cell and the commercial battery from a full cell perspective. An overview of the major challenges, most recent advances, and outlooks of non-aqueous and aqueous sodium-ion full cells (SIFCs) is presented. Considering the intimate relationship between SIFCs and electrode materials, including structure, composition and mutual matching principle, both the advance of various prototype SIFCs and the electrochemistry development of nanostructured electrode materials are reviewed. It is noted that a series of SIFCs combined with layered oxides and hard carbon are capable of providing a high specific gravimetric energy above 200 Wh kg -1 , and an NaCrO 2 //hard carbon full cell is able to deliver a high rate capability over 100 C. To achieve industrialization of SIBs, more systematic work should focus on electrode construction, component compatibility, and battery technologies. © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Study of the collecting electrode material of an extrapolation chamber by Monte Carlo simulation

International Nuclear Information System (INIS)

Vedovato, Uly Pita; Santos, William S.; Perini, Ana Paula; Belinato, Walmir

2017-01-01

In this work, the influence of different materials of the collecting electrode on the response of an extrapolation ionization chamber, was evaluated. This ionization chamber was simulated with the MCNP-4C Monte Carlo code and the spectrum of a standard diagnostic radiology beam (RQR5) was utilized. The different results are due to interactions of photons with different materials of the collecting electrode contributing with different values of energy deposited in the sensitive volume of the ionization chamber, which depends on the atomic number of the evaluated materials. The material that presented the least influence was graphite, the original constituent of the ionization chamber. (author)

Estimation of cerium and lanthanum content in core material of high intensity carbon arc electrodes by x-ray fluorescence method

International Nuclear Information System (INIS)

Nagpal, K.C.; Bhavalkar, R.H.

1977-01-01

The X-ray fluorescence method has been used to determine the weight percentages of cerium and lanthanum in the core material of high intensity carbon arc electrodes from the calibration curves plotted between the weight percentages of these elements and the peak-intensity ratios of CeLsub(α1), and LaLsub(α1) peaks to the neighbouring peak SnLsub(α1) due to an internal standard element. (author)

Transition metal doped poly(aniline-co-pyrrole)/multi-walled carbon nanotubes nanocomposite for high performance supercapacitor electrode materials

Energy Technology Data Exchange (ETDEWEB)

Dhibar, Saptarshi; Bhattacharya, Pallab; Hatui, Goutam; Das, C.K., E-mail: chapal12@yahoo.co.in

2015-03-15

Highlights: • The CuCl{sub 2} doped copolymer (PANI and PPy)/MWCNTs nanocomposite was prepared. • The nanocomposite achieved highest specific capacitance of 383 F/g at a 0.5 A/g. • Nanocomposite exhibits better energy density as well as power density. • The nanocomposite also showed better electrical conductivity at room temperature. • The nanocomposite can be used as promising electrode materials for supercapacitor. - Abstract: In this present communication, copolymer of polyaniline (PANI) and polypyrrole (PPy) that is poly(aniline-co-pyrrole) [poly(An-co-Py)], copper chloride (CuCl{sub 2}) doped poly(aniline-co-pyrrole) [poly(An-co-Py) Cu], and CuCl{sub 2} doped poly(aniline-co-pyrrole)/multi walled carbon nanotubes (MWCNTs) [poly(An-co-Py) Cu CNT] nanocomposite have been prepared by a simple and inexpensive in-situ chemical oxidative polymerization method, using ammonium persulfate (APS) as oxidant and hydrochloric acid (HCl) as dopant and investigated as high performance supercapacitor electrode materials. The possible interaction between CuCl{sub 2} with copolymers and MWCNTs was investigated by Fourier transform infrared spectroscopy (FTIR) and UV–visible spectroscopy analysis. The morphological characteristic of all the electrode materials were analyzed by Field emission scanning electron microscopy (FESEM) and Transmission electron microscopy (TEM) study. The electrochemical characterizations of all the electrode materials were carried out by three electrode probe method where, standard calomel electrode and platinum were used as reference and counter electrodes, respectively. Among all the electrode materials, poly(An-co-Py) Cu CNT nanocomposite achieved highest specific capacitance value of 383 F/g at 0.5 A/g scan rate. The nanocomposite showed better electrical conductivity at room temperature and also attained nonlinear current–voltage characteristic. Based on the superior electrochemical as well as other properties the as prepared

Transition metal doped poly(aniline-co-pyrrole)/multi-walled carbon nanotubes nanocomposite for high performance supercapacitor electrode materials

International Nuclear Information System (INIS)

Dhibar, Saptarshi; Bhattacharya, Pallab; Hatui, Goutam; Das, C.K.

2015-01-01

Highlights: • The CuCl 2 doped copolymer (PANI and PPy)/MWCNTs nanocomposite was prepared. • The nanocomposite achieved highest specific capacitance of 383 F/g at a 0.5 A/g. • Nanocomposite exhibits better energy density as well as power density. • The nanocomposite also showed better electrical conductivity at room temperature. • The nanocomposite can be used as promising electrode materials for supercapacitor. - Abstract: In this present communication, copolymer of polyaniline (PANI) and polypyrrole (PPy) that is poly(aniline-co-pyrrole) [poly(An-co-Py)], copper chloride (CuCl 2 ) doped poly(aniline-co-pyrrole) [poly(An-co-Py) Cu], and CuCl 2 doped poly(aniline-co-pyrrole)/multi walled carbon nanotubes (MWCNTs) [poly(An-co-Py) Cu CNT] nanocomposite have been prepared by a simple and inexpensive in-situ chemical oxidative polymerization method, using ammonium persulfate (APS) as oxidant and hydrochloric acid (HCl) as dopant and investigated as high performance supercapacitor electrode materials. The possible interaction between CuCl 2 with copolymers and MWCNTs was investigated by Fourier transform infrared spectroscopy (FTIR) and UV–visible spectroscopy analysis. The morphological characteristic of all the electrode materials were analyzed by Field emission scanning electron microscopy (FESEM) and Transmission electron microscopy (TEM) study. The electrochemical characterizations of all the electrode materials were carried out by three electrode probe method where, standard calomel electrode and platinum were used as reference and counter electrodes, respectively. Among all the electrode materials, poly(An-co-Py) Cu CNT nanocomposite achieved highest specific capacitance value of 383 F/g at 0.5 A/g scan rate. The nanocomposite showed better electrical conductivity at room temperature and also attained nonlinear current–voltage characteristic. Based on the superior electrochemical as well as other properties the as prepared nanocomposite can be used

Development of materials for open-cycle magnetohydrodynamics (MHD): ceramic electrode. Final report

Energy Technology Data Exchange (ETDEWEB)

Bates, J.L.; Marchant, D.D.

1986-09-01

Pacific Northwest Laboratory, supported by the US Department of Energy, developed advanced materials for use in open-cycle, closed cycle magnetohydrodynamics (MHD) power generation, an advanced energy conversion system in which the flow of electrically conducting fluid interacts with an electric field to convert the energy directly into electricity. The purpose of the PNL work was to develop electrodes for the MHD channel. Such electrodes must have: (1) electrical conductivity above 0.01 (ohm-cm)/sup -1/ from near room temperature to 1900/sup 0/K, (2) resistance to both electrochemical and chemical corrosion by both slag and potassium seed, (3) resistance to erosion by high-velocity gases and particles, (4) resistance to thermal shock, (5) adequate thermal conductivity, (6) compatibility with other channel components, particularly the electrical insulators, (7) oxidation-reduction stability, and (8) adequate thermionic emission. This report describes the concept and development of high-temperature, graded ceramic composite electrode materials and their electrical and structural properties. 47 refs., 16 figs., 13 tabs.

Different types of pre-lithiated hard carbon as negative electrode material for lithium-ion capacitors

International Nuclear Information System (INIS)

Zhang, Jin; Liu, Xifeng; Wang, Jing; Shi, Jingli; Shi, Zhiqiang

2016-01-01

Highlights: • Two types of HC materials with different properties as negative electrode. • Lithium ion intercalation plateau of HC affects electrochemical performance of LIC. • The electrochemical performance of LIC is operated at different potential ranges. • The selection of HC and appropriate potential range of LIC have been proposed. - ABSTRACT: Lithium-ion capacitors (LICs) are assembled with activated carbon (AC) cathode and pre-lithiated hard carbon (HC) anode. Two kinds of HC materials with different physical and electrochemical behaviors have been investigated as the negative electrodes for LIC. Compared with spherical HC, the irregular HC shows a distinct lithium ion intercalation plateau in the charge–discharge process. The existence of lithium ion intercalation plateau for irregular HC greatly affects the electrochemical behavior of HC negative electrode and AC positive electrode. The effect of working potential range on the electrochemical performance of LIC-SH and LIC-IH is investigated by the galvanostatic charging–discharging, electrochemical impedance tests and cycle performance testing. The charge–discharge potential range of the irregular HC negative electrode is lower than the spherical HC electrode due to the existence of lithium ion intercalation plateau, which is conducive to the sufficient utilization of the AC positive electrode. The working potential range of LIC should be controlled to realize the optimization of electrochemical performance of LIC. LIC-IH at the working potential range of 2.0-4.0 V exhibits the optimal electrochemical performance, high energy density up to 85.7 Wh kg −1 and power density as high as 7.6 kW kg −1 (based on active material mass of two electrodes), excellent capacity retention about 96.0% after 5000 cycles.

Facile synthesis of polypyrrole nanowires for high-performance supercapacitor electrode materials

Directory of Open Access Journals (Sweden)

Junhong Zhao

2016-06-01

Full Text Available Polypyrrole nanowires are facile synthesized under a mild condition with FeCl3 as an oxidant. Polypyrrole nanowires with the width of 120 nm form many nanogaps or pores due to the intertwined nanostructures. More importantly, PPy nanowires were further applied for supercapacitor electrode materials. After electrochemical testing, it was observed that the PPy nanowire based electrode showed a large specific capacitance (420 F g−1, 1.5 A g−1 and good rate capability (272 F g−1, 18.0 A g−1, which is larger than that of most of published results. The as-prepared electrode can work well even after 8000 cycles at 1.5 A g−1.

Oriented Polyaniline Nanowire Arrays Grown on Dendrimer (PAMAM) Functionalized Multiwalled Carbon Nanotubes as Supercapacitor Electrode Materials.

Science.gov (United States)

Jin, Lin; Jiang, Yu; Zhang, Mengjie; Li, Honglong; Xiao, Linghan; Li, Ming; Ao, Yuhui

2018-04-19

At present, PANI/MWNT composites have been paid more attention as promising electrode materials in supercapacitors. Yet some shortcomings still limit the widely application of PANI/MWNT electrolytes. In this work, in order to improve capacitance ability and long-term stability of electrode, a multi-amino dendrimer (PAMAM) had been covalently linked onto multi-walled carbon nanotubes (MWNT) as a bridge to facilitating covalent graft of polyaniline (PANI), affording P-MWNT/PANI electrode composites for supercapacitor. Surprisingly, ordered arrays of PANI nanowires on MWNT (setaria-like morphology) had been observed by scanning electron microscopy (SEM). Electrochemical properties of P-MWNT/PANI electrode had been characterized by cyclic voltammetry (CV) and galvanostatic charge-discharge technique. The specific capacitance and long cycle life of P-MWNT-PANI electrode material were both much higher than MWNT/PANI. These interesting results indicate that multi-amino dendrimer, PAMAM, covalently linked on MWNT provides more reaction sites for in-situ polymerization of ordered PANI, which could efficiently shorten the ion diffusion length in electrolytes and lead to making fully use of conducting materials.

Novel synthesis of Ni-ferrite (NiFe2O4) electrode material for supercapacitor applications

International Nuclear Information System (INIS)

Venkatachalam, V.; Jayavel, R.

2015-01-01

Novel nanocrystalline NiFe 2 O 4 has been synthesized through combustion route using citric acid as a fuel. Phase of the synthesized material was analyzed using powder X-ray diffraction. The XRD study revealed the formation of spinel phase cubic NiFe 2 O 4 with high crystallinity. The average crystallite size of NiFe 2 O 4 nanomaterial was calculated from scherrer equation. The electrochemical properties were realized by cyclic voltammetry, chronopotentiometry and electrochemical impedance spectroscopy. The electrode material shows a maximum specific capacitance of 454 F/g with pseudocapacitive behavior. High capacitance retention of electrode material over 1000 continuous charging-discharging cycles suggests its excellent electrochemical stability. The results revealed that the nickel ferrite electrode is a potential candidate for energy storage applications in supercapacitor

Methods for making lithium vanadium oxide electrode materials

Science.gov (United States)

Schutts, Scott M.; Kinney, Robert J.

2000-01-01

A method of making vanadium oxide formulations is presented. In one method of preparing lithium vanadium oxide for use as an electrode material, the method involves: admixing a particulate form of a lithium compound and a particulate form of a vanadium compound; jet milling the particulate admixture of the lithium and vanadium compounds; and heating the jet milled particulate admixture at a temperature below the melting temperature of the admixture to form lithium vanadium oxide.

Development of powder diffraction anomalous fine structure method and applications to electrode materials for rechargeable batteries

International Nuclear Information System (INIS)

Kawaguchi, Tomoya; Fukuda, Katsutoshi; Oishi, Masatsugu; Ichitsubo, Tetsu; Matsubara, Eiichiro; Mizuki, Jun'ichiro

2015-01-01

A powder diffraction anomalous fine structure (P-DAFS) method is developed both in analytical and experimental techniques and applied to cathode materials for lithium ion batteries. The DAFS method, which is an absorption spectroscopic technique through a scattering measurement, enables us to analyze the chemical states and the local structures of a certain element at different sites, thanks to the nature of x-ray diffraction, where the contributions from each site are different at each diffraction. Electrode materials for rechargeable batteries frequently exhibit the interchange between Li and a transition metal, which is known as the cation mixing phenomena. This cation mixing significantly affects the whole electrode properties; therefore, the site-distinguished understanding of the roles of the transition metal is essential for further material design by controlling and positively utilizing this cation mixing phenomenon. However, the developments of the P-DAFS method are required for the applications to the practical materials such as the electrode materials. In the present study, a direct analysis technique to extract the absorption spectrum from the scattering without using the conventional iterative calculations, fast and accurate measurement techniques of the P-DAFS method, and applications to a typical electrode material of Li 1-x Ni 1+x O 2 , which exhibits the significant cation mixing, are described. (author)

Materials and fabrication of electrode scaffolds for deposition of MnO2 and their true performance in supercapacitors

Science.gov (United States)

Cao, Jianyun; Li, Xiaohong; Wang, Yaming; Walsh, Frank C.; Ouyang, Jia-Hu; Jia, Dechang; Zhou, Yu

2015-10-01

MnO2 is a promising electrode material for high energy supercapacitors because of its large pseudo-capacitance. However, MnO2 suffers from low electronic conductivity and poor cation diffusivity, which results in poor utilization and limited rate performance of traditional MnO2 powder electrodes, obtained by pressing a mixed paste of MnO2 powder, conductive additive and polymer binder onto metallic current collectors. Developing binder-free MnO2 electrodes by loading nanoscale MnO2 deposits on pre-fabricated device-ready electrode scaffolds is an effective way to achieve both high power and energy performance. These electrode scaffolds, with interconnected skeletons and pore structures, will not only provide mechanical support and electron collection as traditional current collectors but also fast ion transfer tunnels, leading to high MnO2 utilization and rate performance. This review covers design strategies, materials and fabrication methods for the electrode scaffolds. Rational evaluation of the true performance of these electrodes is carried out, which clarifies that some of the electrodes with as-claimed exceptional performances lack potential in practical applications due to poor mass loading of MnO2 and large dead volume of inert scaffold materials/void spaces in the electrode structure. Possible ways to meet this challenge and bring MnO2 electrodes from laboratory studies to real-world applications are considered.

An Ideal Electrode Material, 3D Surface-Microporous Graphene for Supercapacitors with Ultrahigh Areal Capacitance

International Nuclear Information System (INIS)

Chang, Liang; Stacchiola, Dario J.; Hu, Yun Hang

2017-01-01

The efficient charge accumulation of an ideal supercapacitor electrode requires abundant micropores and its fast electrolyte-ions transport prefers meso/macropores. But, current electrode materials cannot meet both requirements, resulting in poor performance. We creatively constructed three-dimensional cabbage-coral-like graphene as an ideal electrode material, in which meso/macro channels are formed by graphene walls and rich micropores are incorporated in the surface layer of the graphene walls. The unique 3D graphene material can achieve a high gravimetric capacitance of 200 F/g with aqueous electrolyte, 3 times larger than that of commercially used activated carbon (70.8 F/g). Furthermore, it can reach an ultrahigh areal capacitance of 1.28 F/cm"2 and excellent rate capability (83.5% from 0.5 to 10 A/g) as well as high cycling stability (86.2% retention after 5000 cycles). The excellent electric double-layer performance of the 3D graphene electrode can be attributed to the fast electrolyte ion transport in the meso/macro channels and the rapid and reversible charge adsorption with negligible transport distance in the surface micropores.

A study of nitroxide polyradical/activated carbon composite as the positive electrode material for electrochemical hybrid capacitor

Energy Technology Data Exchange (ETDEWEB)

Li, Hui-qiao; Zou, Ying; Xia, Yong-yao [Chemistry Department and Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Fudan University, Shanghai 200433 (China)

2007-01-01

We present a new concept of the hybrid electrochemical capacitor technology in which a poly(2,2,6,6-tetramethylpiperidinyloxy methacrylate) nitroxide polyradical/activated carbon composite (PTMA-AC) is used as the positive electrode material and activated carbon is used as the negative electrode material. On the positive electrode, both reversible reduction and oxidation of nitroxide polyradical and non-faradic ion sorption/de-sorption of activated carbon are involved during charge and discharge process. The capacity of the composite electrode is 30% larger than that of the pure activated carbon electrode. A hybrid capacitor fabricated by the PTMA-AC composite positive electrode and the activated carbon negative electrode shows a good cycling life, it can be charged/discharged for over 1000 cycles with slight capacity loss. The hybrid capacitor also has a good rate capability, it maintains 80% of the initial capacity even at the high discharge current of up to 20C. (author)

Facile synthesis of polypyrrole nanowires for high-performance supercapacitor electrode materials

OpenAIRE

Zhao, Junhong; Wu, Jinping; Li, Bing; Du, Weimin; Huang, Qingli; Zheng, Mingbo; Xue, Huaiguo; Pang, Huan

2016-01-01

Polypyrrole nanowires are facile synthesized under a mild condition with FeCl3 as an oxidant. Polypyrrole nanowires with the width of 120 nm form many nanogaps or pores due to the intertwined nanostructures. More importantly, PPy nanowires were further applied for supercapacitor electrode materials. After electrochemical testing, it was observed that the PPy nanowire based electrode showed a large specific capacitance (420 F g−1, 1.5 A g−1) and good rate capability (272 F g−1, 18.0 A g−1), wh...

Nanostructured Mo-based electrode materials for electrochemical energy storage.

Science.gov (United States)

Hu, Xianluo; Zhang, Wei; Liu, Xiaoxiao; Mei, Yueni; Huang, Yunhui

2015-04-21

The development of advanced energy storage devices is at the forefront of research geared towards a sustainable future. Nanostructured materials are advantageous in offering huge surface to volume ratios, favorable transport features, and attractive physicochemical properties. They have been extensively explored in various fields of energy storage and conversion. This review is focused largely on the recent progress in nanostructured Mo-based electrode materials including molybdenum oxides (MoO(x), 2 ≤ x ≤ 3), dichalconides (MoX2, X = S, Se), and oxysalts for rechargeable lithium/sodium-ion batteries, Mg batteries, and supercapacitors. Mo-based compounds including MoO2, MoO3, MoO(3-y) (0 energy storage systems because of their unique physicochemical properties, such as conductivity, mechanical and thermal stability, and cyclability. In this review, we aim to provide a systematic summary of the synthesis, modification, and electrochemical performance of nanostructured Mo-based compounds, as well as their energy storage applications in lithium/sodium-ion batteries, Mg batteries, and pseudocapacitors. The relationship between nanoarchitectures and electrochemical performances as well as the related charge-storage mechanism is discussed. Moreover, remarks on the challenges and perspectives of Mo-containing compounds for further development in electrochemical energy storage applications are proposed. This review sheds light on the sustainable development of advanced rechargeable batteries and supercapacitors with nanostructured Mo-based electrode materials.

High-Performance Supercapacitor Electrode Materials from Cellulose-Derived Carbon Nanofibers.

Science.gov (United States)

Cai, Jie; Niu, Haitao; Li, Zhenyu; Du, Yong; Cizek, Pavel; Xie, Zongli; Xiong, Hanguo; Lin, Tong

2015-07-15

Nitrogen-functionalized carbon nanofibers (N-CNFs) were prepared by carbonizing polypyrrole (PPy)-coated cellulose NFs, which were obtained by electrospinning, deacetylation of electrospun cellulose acetate NFs, and PPy polymerization. Supercapacitor electrodes prepared from N-CNFs and a mixture of N-CNFs and Ni(OH)2 showed specific capacitances of ∼236 and ∼1045 F g(-1), respectively. An asymmetric supercapacitor was further fabricated using N-CNFs/Ni(OH)2 and N-CNFs as positive and negative electrodes. The supercapacitor device had a working voltage of 1.6 V in aqueous KOH solution (6.0 M) with an energy density as high as ∼51 (W h) kg(-1) and a maximum power density of ∼117 kW kg(-1). The device had excellent cycle lifetime, which retained ∼84% specific capacitance after 5000 cycles of cyclic voltammetry scans. N-CNFs derived from electrospun cellulose may be useful as an electrode material for development of high-performance supercapacitors and other energy storage devices.

Research Progress in MnO2 -Carbon Based Supercapacitor Electrode Materials.

Science.gov (United States)

Zhang, Qun-Zheng; Zhang, Dian; Miao, Zong-Cheng; Zhang, Xun-Li; Chou, Shu-Lei

2018-04-30

With the serious impact of fossil fuels on the environment and the rapid development of the global economy, the development of clean and usable energy storage devices has become one of the most important themes of sustainable development in the world today. Supercapacitors are a new type of green energy storage device, with high power density, long cycle life, wide temperature range, and both economic and environmental advantages. In many industries, they have enormous application prospects. Electrode materials are an important factor affecting the performance of supercapacitors. MnO 2 -based materials are widely investigated for supercapacitors because of their high theoretical capacitance, good chemical stability, low cost, and environmental friendliness. To achieve high specific capacitance and high rate capability, the current best solution is to use MnO 2 and carbon composite materials. Herein, MnO 2 -carbon composite as supercapacitor electrode materials is reviewed including the synthesis method and research status in recent years. Finally, the challenges and future development directions of an MnO 2 -carbon based supercapacitor are summarized. © 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Few-layered CoHPO4.3H2O ultrathin nanosheets for high performance of electrode materials for supercapacitors

Science.gov (United States)

Pang, Huan; Wang, Shaomei; Shao, Weifang; Zhao, Shanshan; Yan, Bo; Li, Xinran; Li, Sujuan; Chen, Jing; Du, Weimin

2013-06-01

Ultrathin cobalt phosphate (CoHPO4.3H2O) nanosheets are successfully synthesized by a one pot hydrothermal method. Novel CoHPO4.3H2O ultrathin nanosheets are assembled for constructing the electrodes of supercapacitors. Benefiting from the nanostructures, the as-prepared electrode shows a specific capacitance of 413 F g-1, and no obvious decay even after 3000 charge-discharge cycles. Such a quasi-two-dimensional material is a new kind of supercapacitor electrode material with high performance.Ultrathin cobalt phosphate (CoHPO4.3H2O) nanosheets are successfully synthesized by a one pot hydrothermal method. Novel CoHPO4.3H2O ultrathin nanosheets are assembled for constructing the electrodes of supercapacitors. Benefiting from the nanostructures, the as-prepared electrode shows a specific capacitance of 413 F g-1, and no obvious decay even after 3000 charge-discharge cycles. Such a quasi-two-dimensional material is a new kind of supercapacitor electrode material with high performance. Electronic supplementary information (ESI) available. See DOI: 10.1039/c3nr01460f

A MEMS platform for in situ, real-time monitoring of electrochemically induced mechanical changes in lithium-ion battery electrodes

International Nuclear Information System (INIS)

Pomerantseva, Ekaterina; Jung, Hyun; Gnerlich, Markus; Baron, Sergio; Gerasopoulos, Konstantinos; Ghodssi, Reza

2013-01-01

We report the first successful demonstration of an optical microelectromechanical systems (MEMS) sensing platform for the in situ characterization of electrochemically induced reversible mechanical changes in lithium-ion battery (LIB) electrodes. The platform consists of an array of flexible membranes with a reflective surface on one side and a thin-film LIB electrode on the other side. The membranes deflect due to the active battery material volume change caused by lithium intercalation (expansion) and extraction (contraction). This deflection is monitored using the Fabry–Perot optical interferometry principle. The active material volume change causes high internal stresses and mechanical degradation of the electrodes. The stress evolution observed in a silicon thin-film electrode incorporated into this MEMS platform follows a ‘first elastic, then plastic’ deformation scheme. Understanding of the internal stresses in battery electrodes during discharge/charge is important for improving the reliability and cycle lifetime of LIBs. The developed MEMS platform presents a new method for in situ diagnostics of thin-film LIB electrodes to aid the development of new materials, optimization of electrode performance, and prevention of battery failure. (paper)

Two-dimensional hierarchical porous carbon composites derived from corn stalks for electrode materials with high performance

International Nuclear Information System (INIS)

Xu, Haitao; Zhang, Huijuan; Ouyang, Ya; Liu, Li; Wang, Yu

2016-01-01

Highlights: • Novel 2D porous carbon sheets from cornstalks are obtained for the first time. • The hierarchical porous carbon nansheets are gained by chemical activation. • The porous structure facilitates ion transfer and Li-ion absorption. • The strategy are applied to both cathode and anode electrode materials. • The porous nanocomposites exhibit excellent electrochemical performance. - Abstract: Herein, we propose a novel and green strategy to convert crop stalks waste into hierarchical porous carbon composites for electrode materials of lithium-ion batteries. In the method, the sustainable crop stalks, an abundant agricultural byproduct, is recycled and treated by a simple and clean chemical activation process. Afterwards, the obtained porous template is adopted for large-scale production of high-performance anode and cathode materials for lithium-ion batteries. Due to the large surface area, hierarchical porous structures and subsize of the functional particles, the electrode materials manifest excellent electrochemical performance. In particular, the prepared TiO 2 /C composite presents a reversible specific capacity of 203 mAh g −1 after 200 cycles. Our results demonstrate that the sheetlike composites show remarkable cycling stability, high specific capacity and excellent rate ability, and thus hold promise for commercializing the high-performance electrode materials as the advanced lithium-ion batteries.

Porphyrin doped vanadium pentoxide xerogel as electrode material

Energy Technology Data Exchange (ETDEWEB)

Anaissi, F.J.; Engelmann, F.M.; Araki, K.; Toma, H.E. [Sao Paulo Univ., SP (Brazil). Inst. de Quimica

2003-04-01

The lamellar composite material, VXG-TMPyP, obtained from the combination of cationic, water-soluble meso-(tetra-4-methyl-pyridinium)porphyrin (TMPyP) and vanadium pentoxide gel was investigated and employed as electrode modifying material. This material was isolated as a xerogel and characterized by X-ray diffraction, UV-Vis spectroscopy, cyclic voltammetry, spectro-electrochemistry and TG analysis. According to the X-ray diffraction data, the original VXG lamellar matrix framework is kept in the composite, evidencing a topotatic reaction. UV-Vis spectra indicated a strong interaction between VXG and TMPyP leading to the protonation of the porphyrin ring. In contrast with the vanadium oxide xerogel the new material is stable in water. The presence of the cationic porphyrin species in its structure turns it able to incorporate negatively charged ions, such as ferrocyanide and I{sup -}. The presence of the I{sub 2}/I{sup -} couple gives rise to a dramatic increase in the reversibility of the V{sup V/IV} process and in the charge capacity of the material. (authors)

Surface modification of positive electrode materials for lithium-ion batteries

Energy Technology Data Exchange (ETDEWEB)

Julien, C.M., E-mail: Christian.Julien@upmc.fr [Sorbonne Universités, UPMC Univ. Paris 6, Physicochimie des Electrolytes et Nanosystèmes Interfaciaux (PHENIX), UMR 8234, 75005 Paris (France); Mauger, A. [Institut de Minéralogie de Physique des Matériaux et de Cosmochimie (IMPMC), UPMC Univ. Paris 6, 4 place Jussieu, 75005 Paris (France); Groult, H. [Sorbonne Universités, UPMC Univ. Paris 6, Physicochimie des Electrolytes et Nanosystèmes Interfaciaux (PHENIX), UMR 8234, 75005 Paris (France); Zaghib, K. [Energy Storage and Conversion, Research Institute of Hydro-Québec, Varennes, Québec J3X 1S1 (Canada)

2014-12-01

The advanced lithium-ion batteries are critically important for a wide range of applications, from portable electronics to electric vehicles. The research on their electrodes aims to increase the energy density and the power density, improve the calendar and the cycling life, without sacrificing the safety issues. A constant progress through the years has been obtained owing to the surface treatment of the particles, in particular the coating of the nanoparticles with a layer that protects the core region from side reactions with the electrolyte, prevents the loss of oxygen, and the dissolution of the metal ions in the electrolyte, or simply improve the conductivity of the powder. The purpose of the present work is to present the different surface modifications that have been tried for three families of positive electrodes: layered, spinel and olivine frameworks that are currently considered as promising materials. The role of the different coats used to improve either the surface conductivity, or the thermal stability, or the structural integrity is discussed. - Highlights: • Report the various surface modifications tried for the positive electrodes of Li-ion batteries. • The role of different coats used to improve the conductivity, or the thermal stability, or the structural integrity. • Improvement of electrochemical properties of electrodes after coating or surface treatment.

Graphene/MnO2 hybrid nanosheets as high performance electrode materials for supercapacitors

International Nuclear Information System (INIS)

Mondal, Anjon Kumar; Wang, Bei; Su, Dawei; Wang, Ying; Chen, Shuangqiang; Zhang, Xiaogang; Wang, Guoxiu

2014-01-01

Graphene/MnO 2 hybrid nanosheets were prepared by incorporating graphene and MnO 2 nanosheets in ethylene glycol. Scanning electron microscopy and transmission electron microscopy analyses confirmed nanosheet morphology of the hybrid materials. Graphene/MnO 2 hybrid nanosheets with different ratios were investigated as electrode materials for supercapacitors by cyclic voltammetry (CV) and galvanostatic charge–discharge in 1 M Na 2 SO 4 electrolyte. We found that the graphene/MnO 2 hybrid nanosheets with a weight ratio of 1:4 (graphene:MnO 2 ) delivered the highest specific capacitance of 320 F g −1 . Graphene/MnO 2 hybrid nanosheets also exhibited good capacitance retention on 2000 cycles. - Highlights: • Graphene/MnO 2 hybrid nanosheets with different ratios were fabricated. • The specific capacitance is strongly dependent on graphene/MnO 2 ratios. • The graphene/MnO 2 hybrid electrode (1:4) exhibited high specific capacitance. • The electrode retained 84% of the initial specific capacitance after 2000 cycles

NiO nanosheet assembles for supercapacitor electrode materials

OpenAIRE

Huanhao Xiao; Shunyu Yao; Hongda Liu; Fengyu Qu; Xu Zhang; Xiang Wu

2016-01-01

In this paper, large scale hierarchically assembled NiO nanosheets have been favorably fabricated through a facile hydrothermal route. The as-prepared NiO nanosheet assembles were characterized in detail by various analytical techniques. The results showed these nanosheets present the thickness of about 30 nm and the surface area is 116.9 m2 g−1. These NiO nanosheet assembles were used as the working electrode materials in electrochemical tests, which demonstrated a specific capacitance value...

Synthesis and characterization of NiCo_2O_4 nanoplates as efficient electrode materials for electrochemical supercapacitors

International Nuclear Information System (INIS)

Kim, Taehyun; Ramadoss, Ananthakumar; Saravanakumar, Balasubramaniam; Veerasubramani, Ganesh Kumar; Kim, Sang Jae

2016-01-01

Highlights: • NiCo_2O_4 nanoplates were synthesized through a facile approach. • The NiCo_2O_4 nanoplates electrode material exhibit a specific capacitance of 332 F g"−"1 at 5 mV s"−"1. • The fabricated NiCo_2O_4 electrode reveals 86% retention of initial capacitance after 2000 cycles. - Abstract: In the present work, NiCo_2O_4 nanoplates were prepared by a facile, low temperature, hydrothermal method, followed by thermal annealing and used supercapacitor applications. The physico-chemical characterization of as-prepared materials were investigated by means of X-ray diffraction (XRD), Fourier transform infra-red spectroscopy (FT-IR) and field emission scanning electron microscopy (FE-SEM). The electrochemical measurements demonstrate that the NiCo_2O_4 nanoplates electrode (NC-5) exhibits a high specific capacitance of 332 F g"−"1 at a scan rate of 5 mV s"−"1 and also retained about 86% of the initial specific capacitance value even after 2000 cycles at a current density of 2.5 A g"−"1. These results suggest that the fabricated electrode material has huge potential as a novel electrode material for electrochemical capacitors.

Environmental Screening of Electrode Materials for a Rechargeable Aluminum Battery with an AlCl3/EMIMCl Electrolyte

Directory of Open Access Journals (Sweden)

Linda Ager-Wick Ellingsen

2018-06-01

Full Text Available Recently, rechargeable aluminum batteries have received much attention due to their low cost, easy operation, and high safety. As the research into rechargeable aluminum batteries with a room-temperature ionic liquid electrolyte is relatively new, research efforts have focused on finding suitable electrode materials. An understanding of the environmental aspects of electrode materials is essential to make informed and conscious decisions in aluminum battery development. The purpose of this study was to evaluate and compare the relative environmental performance of electrode material candidates for rechargeable aluminum batteries with an AlCl3/EMIMCl (1-ethyl-3-methylimidazolium chloride room-temperature ionic liquid electrolyte. To this end, we used a lifecycle environmental screening framework to evaluate 12 candidate electrode materials. We found that all of the studied materials are associated with one or more drawbacks and therefore do not represent a “silver bullet” for the aluminum battery. Even so, some materials appeared more promising than others did. We also found that aluminum battery technology is likely to face some of the same environmental challenges as Li-ion technology but also offers an opportunity to avoid others. The insights provided here can aid aluminum battery development in an environmentally sustainable direction.

Impedance spectroscopic analysis of composite electrode from activated carbon/conductive materials/ruthenium oxide for supercapacitor applications

Energy Technology Data Exchange (ETDEWEB)

Taer, E.; Awitdrus,; Farma, R. [School of Applied Physics, Faculty of Science and Technology, Universiti Kebangsaan Malaysia, 43600 Bangi, Selangor (Malaysia); Department of Physics, Faculty of Mathematics and Natural Sciences, University of Riau, 28293 Pekanbaru, Riau (Indonesia); Deraman, M., E-mail: madra@ukm.my; Talib, I. A.; Ishak, M. M.; Omar, R.; Dolah, B. N. M.; Basri, N. H.; Othman, M. A. R. [School of Applied Physics, Faculty of Science and Technology, Universiti Kebangsaan Malaysia, 43600 Bangi, Selangor (Malaysia); Kanwal, S. [ICCBS, H.E.J. Research Institute of Chemistry, University of Karachi, 75270 Karachi (Pakistan)

2015-04-16

Activated carbon powders (ACP) were produced from the KOH treated pre-carbonized rubber wood sawdust. Different conductive materials (graphite, carbon black and carbon nanotubes (CNTs)) were added with a binder (polivinylidene fluoride (PVDF)) into ACP to improve the supercapacitive performance of the activated carbon (AC) electrodes. Symmetric supercapacitor cells, fabricated using these AC electrodes and 1 molar H{sub 2}SO{sub 4} electrolyte, were analyzed using a standard electrochemical impedance spectroscopy technique. The addition of graphite, carbon black and CNTs was found effective in reducing the cell resistance from 165 to 68, 23 and 49 Ohm respectively, and increasing the specific capacitance of the AC electrodes from 3 to 7, 17, 32 F g{sup −1} respectively. Since the addition of CNTs can produce the highest specific capacitance, CNTs were chosen as a conductive material to produce AC composite electrodes that were added with 2.5 %, 5 % and 10 % (by weight) electro-active material namely ruthenium oxide; PVDF binder and CNTs contents were kept at 5 % by weight in each AC composite produced. The highest specific capacitance of the cells obtained in this study was 86 F g{sup −1}, i.e. for the cell with the resistance of 15 Ohm and composite electrode consists of 5 % ruthenium oxide.

Effect of Start-Up Strategies and Electrode Materials on Carbon Dioxide Reduction on Biocathodes.

Science.gov (United States)

Saheb-Alam, Soroush; Singh, Abhijeet; Hermansson, Malte; Persson, Frank; Schnürer, Anna; Wilén, Britt-Marie; Modin, Oskar

2018-02-15

The enrichment of CO 2 -reducing microbial biocathodes is challenging. Previous research has shown that a promising approach could be to first enrich bioanodes and then lower the potential so the electrodes are converted into biocathodes. However, the effect of such a transition on the microbial community on the electrode has not been studied. The goal of this study was thus to compare the start-up of biocathodes from preenriched anodes with direct start-up from bare electrodes and to investigate changes in microbial community composition. The effect of three electrode materials on the long-term performance of the biocathodes was also investigated. In this study, preenrichment of acetate-oxidizing bioanodes did not facilitate the start-up of biocathodes. It took about 170 days for the preenriched electrodes to generate substantial cathodic current, compared to 83 days for the bare electrodes. Graphite foil and carbon felt cathodes produced higher current at the beginning of the experiment than did graphite rods. However, all electrodes produced similar current densities at the end of the over 1-year-long study (2.5 A/m 2 ). Methane was the only product detected during operation of the biocathodes. Acetate was the only product detected after inhibition of the methanogens. Microbial community analysis showed that Geobacter sp. dominated the bioanodes. On the biocathodes, the Geobacter sp. was succeeded by Methanobacterium spp., which made up more than 80% of the population. After inhibition of the methanogens, Acetobacterium sp. became dominant on the electrodes (40% relative abundance). The results suggested that bioelectrochemically generated H 2 acted as an electron donor for CO 2 reduction. IMPORTANCE In microbial electrochemical systems, living microorganisms function as catalysts for reactions on the anode and/or the cathode. There is a variety of potential applications, ranging from wastewater treatment and biogas generation to production of chemicals. Systems

Role of material properties and mechanical constraint on stress-assisted diffusion in plate electrodes of lithium ion batteries

International Nuclear Information System (INIS)

Song Yicheng; Zhang Junqian; Shao Xianjun; Guo Zhansheng

2013-01-01

This work investigates the stress-assisted diffusion of lithium ions in layered electrodes of Li-ion batteries. Decoupled diffusion governing equations are obtained. Material properties, which are characterized by a single dimensionless parameter, and mechanical constraint between a current collector and an active layer, which is characterized by the elastic modulus ratio and thickness ratio between the layers, are identified as key factors that govern the stress-assisted diffusion. For a symmetric plate electrode, stress is induced by the Li-ion concentration gradient, and stress-assisted diffusion therefore depends only on the material properties. For an asymmetric bilayer electrode, mechanical constraint plays a very important role in the diffusion via generation of bending stress. Diffusion may be facilitated, or inversely impeded, according to the constraint. By summarizing the coupling factors of common active materials and investigating the concentration variation induced by stress-assisted diffusion in various electrodes, this work provides insights on stress-assisted diffusion in a layered electrode, as well as suggestions for relevant modelling works on whether the stress-assisted diffusion should be taken into account according to the selection of material and structure. (paper)

International handling of fissionable material

International Nuclear Information System (INIS)

1975-01-01

The opinion of the ministry for foreign affairs on international handling of fissionable materials is given. As an introduction a survey is given of the possibilities to produce nuclear weapons from materials used in or produced by power reactors. Principles for international control of fissionable materials are given. International agreements against proliferation of nuclear weapons are surveyed and methods to improve them are proposed. (K.K.)

Selective observation of charge storing ions in supercapacitor electrode materials.

Science.gov (United States)

Forse, Alexander C; Griffin, John M; Grey, Clare P

2018-02-01

Nuclear magnetic resonance (NMR) spectroscopy has emerged as a useful technique for probing the structure and dynamics of the electrode-electrolyte interface in supercapacitors, as ions inside the pores of the carbon electrodes can be studied separately from bulk electrolyte. However, in some cases spectral resolution can limit the information that can be obtained. In this study we address this issue by showing how cross polarisation (CP) NMR experiments can be used to selectively observe the in-pore ions in supercapacitor electrode materials. We do this by transferring magnetisation from 13 C nuclei in porous carbons to nearby nuclei in the cations ( 1 H) or anions ( 19 F) of an ionic liquid. Two-dimensional NMR experiments and CP kinetics measurements confirm that in-pore ions are located within Ångströms of sp 2 -hybridised carbon surfaces. Multinuclear NMR experiments hold promise for future NMR studies of supercapacitor systems where spectral resolution is limited. Copyright © 2017 University of Cambridge. Published by Elsevier Inc. All rights reserved.

CAPACITANCE OF SUPERCAPACITORS WITH ELECTRODES BASED ON CARBON NANOCOMPOSITE MATERIAL

OpenAIRE

S.L Revo; B.I Rachiy; S Hamamda; T.G Avramenko; K.O Ivanenko

2012-01-01

This work presents the results of our research of the structure and practically important characteristics of a nanocomposite material on the basis of nanoporous carbon and thermally exfoliated graphite. This work shows that the use of the abovementioned composition in electrodes for supercapacitors allows to attain the level of their specific electrical capacitance at (155...160) F/g.

Electrochemical properties of high-power supercapacitors using ordered NiO coated Si nanowire array electrodes

Science.gov (United States)

Lu, Fang; Qiu, Mengchun; Qi, Xiang; Yang, Liwen; Yin, Jinjie; Hao, Guolin; Feng, Xiang; Li, Jun; Zhong, Jianxin

2011-08-01

Highly ordered NiO coated Si nanowire arrays are fabricated as electrode materials for electrochemical supercapacitors (ES) via depositing Ni on electroless-etched Si nanowires and subsequently annealing. The electrochemical tests reveal that the constructed electrode has superior electrical conductibility and more active sites per unit area for chemical reaction processes, thereby possessing good cycle stability, high specific capacity, and low internal resistance. The specific capacity is up to 787.5 F g-1 at a discharge current of 2.5 mA and decreases slightly with 4.039% loss after 500 cycles, while the equivalent internal resistance is ˜3.067 Ω. Owing to its favorable electrochemical performance, this ordered hybrid array nanostructure is a promising electrode material in future commercial ES.

Synthesis and characterization of high performance electrode materials for lithium ion batteries

Science.gov (United States)

Hong, Jian

Lithium-ion batteries have revolutionized portable electronics. Electrode reactions in these electrochemical systems are based on reversible intercalation of Li+ ions into the host electrode material with a concomitant addition/removal of electrons into the host. If such batteries are to find a wider market such as the automotive industry, less expensive and higher capacity electrode materials will be required. The olivine phase lithium iron phosphate has attracted the most attention because of its low cost and safety (high thermal and chemical stability). However, it is an intriguing fundamental problem to understand the fast electrochemical response from the poorly electronic conducting two-phase LiFePO4/FePO 4 system. This thesis focuses on determining the rate-limit step of LiFePO4. First, a LiFePO4 material, with vanadium substituting on the P-site, was synthesized, and found that the crystal structure change may cause high lithium diffusivity. Since an accurate Li diffusion coefficient cannot be measured by traditional electrochemical method in a three-electrode cell due to the phase transformation during measurement, a new method to measure the intrinsic electronic and ionic conductivity of mixed conductive LiFePO 4 was developed. This was based on the conductivity measurements of mixed conductive solid electrolyte using electrochemical impedance spectroscopy (EIS) and blocking electrode. The effects of ionic/electronic conductivity and phase transformation on the rate performance of LiFePO4 were also first investigated by EIS and other electrochemical technologies. Based on the above fundamental kinetics studies, an optimized LiFePO4 was used as a target to deposit 1mum LiFePO4 thin film at Oak Ridge National Laboratory using radio frequency (RF) magnetron sputtering. Similar to the carbon coated LiFePO4 powder electrode, the carbon-contained RF LiFePO4 film with no preferential orientation showed excellent capacity and rate capability both at 25°C and -20

Nanostructured Electrode Materials for Electrochemical Capacitor Applications.

Science.gov (United States)

Choi, Hojin; Yoon, Hyeonseok

2015-06-02

The advent of novel organic and inorganic nanomaterials in recent years, particularly nanostructured carbons, conducting polymers, and metal oxides, has enabled the fabrication of various energy devices with enhanced performance. In this paper, we review in detail different nanomaterials used in the fabrication of electrochemical capacitor electrodes and also give a brief overview of electric double-layer capacitors, pseudocapacitors, and hybrid capacitors. From a materials point of view, the latest trends in electrochemical capacitor research are also discussed through extensive analysis of the literature and by highlighting notable research examples (published mostly since 2013). Finally, a perspective on next-generation capacitor technology is also given, including the challenges that lie ahead.

Physics of electron and lithium-ion transport in electrode materials for Li-ion batteries

International Nuclear Information System (INIS)

Wu Musheng; Xu Bo; Ouyang Chuying

2016-01-01

The physics of ionic and electrical conduction at electrode materials of lithium-ion batteries (LIBs) are briefly summarized here, besides, we review the current research on ionic and electrical conduction in electrode material incorporating experimental and simulation studies. Commercial LIBs have been widely used in portable electronic devices and are now developed for large-scale applications in hybrid electric vehicles (HEV) and stationary distributed power stations. However, due to the physical limits of the materials, the overall performance of today’s LIBs does not meet all the requirements for future applications, and the transport problem has been one of the main barriers to further improvement. The electron and Li-ion transport behaviors are important in determining the rate capacity of LIBs. (topical review)

Electrocolorimetry of electrochromic materials on flexible ITO electrodes

Energy Technology Data Exchange (ETDEWEB)

Pinheiro, Carlos [Requimte, Dep. Quimica, FCT, Universidade Nova de Lisboa, 2829-516 Caparica (Portugal); YDreams, Madan Parque, Quinta da Torre, 2829-516 Caparica (Portugal); Parola, A.J.; Pina, F. [Requimte, Dep. Quimica, FCT, Universidade Nova de Lisboa, 2829-516 Caparica (Portugal); Fonseca, J.; Freire, C. [Requimte, Dep. Quimica, Faculdade de Ciencias, Universidade do Porto, Rua do Campo Alegre, 4169-007 Porto (Portugal)

2008-08-15

Electrochromic materials are characterized by their colour changes upon applied voltage. Colour can mean many things: a certain kind of light, its effect on the human eye, or the result of this effect in the mind of the viewer. Since the electrochromic materials are developed towards real life applications it is relevant to characterize them with the usual commercial colour standards. A colorimetric study of electrogenerated Prussian blue and electrogenerated polymers based on salen-type complexes of Cu(II), Ni(II) and Pd(II) deposited over transparent flexible electrodes of polyethylene terephthalate coated with indium tin oxide (PET/ITO electrodes) was carried out using the CIELAB coordinates. A cuvette with a designed adapter to allow potentiostatic control was placed on an integrating sphere installed in the sample compartment of a spectrophotometer to run the colorimetric measurements. The colour evolution in situ was measured through the transmittance of the films by potentiostatic control. Chronocoulometry/chronoabsorptometry was used to evaluate maximum coloration efficiencies for the coloration step: 184 (Pd), 161 (Cu) and 83 cm{sup 2}/C (Ni) and for bleaching: 199 (Pd), 212 (Cu) and 173 cm{sup 2}/C (Ni) of the Pd, Cu and Ni polymer films, respectively. The Prussian Blue/Prussian White states over the PET/ITO films were relatively reversible while the reversibility and stability of the polymers based on the metals salen-type complexes depends on the metal, Pd being the most stable. (author)

Electrosynthesis and catalytic activity of polymer-nickel particles composite electrode materials

International Nuclear Information System (INIS)

Melki, Tahar; Zouaoui, Ahmed; Bendemagh, Barkahoum; Oliveira, Ione M.F. de; Oliveira, Gilver F. de; Lepretre, Jean-Claude; Bucher, Christophe; Mou tet, Jean-Claude

2009-01-01

Nickel-polymer composite electrode materials have been synthesized using various strategies, all comprising the electrochemical reduction of nickel(II) cations or complexes, incorporated by either ion-exchange or complexation into various poly(pyrrole-carboxylate) thin films coated by oxidative electropolymerization onto carbon electrodes. The electrocatalytic activity and the stability of the different composites have been then evaluated in the course of the electrocatalytic hydrogenation of ketones and enones in aqueous electrolytes. The best results were obtained using nickel-polymer composites synthesized by electroreduction of nickel(II) ions complexed into polycarboxylate films, which are characterized by a high catalytic activity and a good operational stability. (author)

Electrosynthesis and catalytic activity of polymer-nickel particles composite electrode materials

Energy Technology Data Exchange (ETDEWEB)

Melki, Tahar; Zouaoui, Ahmed; Bendemagh, Barkahoum [Universite Ferhat Abbas, Setif (Algeria). Faculte des Sciences de l' Ingenieur. Dept. du Tronc Commun; Oliveira, Ione M.F. de; Oliveira, Gilver F. de [Universidade Federal de Minas Gerais (UFMG), Belo Horizonte, MG (Brazil). Dept. de Quimica; Lepretre, Jean-Claude [UMR-5631 CNRS-INPG-UJF, St. Martin d' Heres Cedex (France). Lab. d' Electrochimie et de Physicochimie des Materiaux et Interfaces; Bucher, Christophe; Mou tet, Jean-Claude [Universite Joseph Fourier Grenoble 1 (France). Dept. de Chimie Moleculaire], e-mail: Jean-Claude.Moutet@ujf-grenoble.fr

2009-07-01

Nickel-polymer composite electrode materials have been synthesized using various strategies, all comprising the electrochemical reduction of nickel(II) cations or complexes, incorporated by either ion-exchange or complexation into various poly(pyrrole-carboxylate) thin films coated by oxidative electropolymerization onto carbon electrodes. The electrocatalytic activity and the stability of the different composites have been then evaluated in the course of the electrocatalytic hydrogenation of ketones and enones in aqueous electrolytes. The best results were obtained using nickel-polymer composites synthesized by electroreduction of nickel(II) ions complexed into polycarboxylate films, which are characterized by a high catalytic activity and a good operational stability. (author)

Carbon Paste Electrodes Made from Different Carbonaceous Materials: Application in the Study of Antioxidants

Science.gov (United States)

Apetrei, Constantin; Apetrei, Irina Mirela; De Saja, Jose Antonio; Rodriguez-Mendez, Maria Luz

2011-01-01

This work describes the sensing properties of carbon paste electrodes (CPEs) prepared from three different types of carbonaceous materials: graphite, carbon microspheres and carbon nanotubes. The electrochemical responses towards antioxidants including vanillic acid, catechol, gallic acid, l-ascorbic acid and l-glutathione have been analyzed and compared. It has been demonstrated that the electrodes based on carbon microspheres show the best performances in terms of kinetics and stability, whereas G-CPEs presented the smallest detection limit for all the antioxidants analyzed. An array of electrodes has been constructed using the three types of electrodes. As demonstrated by means of Principal Component Analysis, the system is able to discriminate among antioxidants as a function of their chemical structure and reactivity. PMID:22319354

Molecular Engineering with Organic Carbonyl Electrode Materials for Advanced Stationary and Redox Flow Rechargeable Batteries.

Science.gov (United States)

Zhao, Qing; Zhu, Zhiqiang; Chen, Jun

2017-12-01

Organic carbonyl electrode materials that have the advantages of high capacity, low cost and being environmentally friendly, are regarded as powerful candidates for next-generation stationary and redox flow rechargeable batteries (RFBs). However, low carbonyl utilization, poor electronic conductivity and undesired dissolution in electrolyte are urgent issues to be solved. Here, we summarize a molecular engineering approach for tuning the capacity, working potential, concentration of active species, kinetics, and stability of stationary and redox flow batteries, which well resolves the problems of organic carbonyl electrode materials. As an example, in stationary batteries, 9,10-anthraquinone (AQ) with two carbonyls delivers a capacity of 257 mAh g -1 (2.27 V vs Li + /Li), while increasing the number of carbonyls to four with the formation of 5,7,12,14-pentacenetetrone results in a higher capacity of 317 mAh g -1 (2.60 V vs Li + /Li). In RFBs, AQ, which is less soluble in aqueous electrolyte, reaches 1 M by grafting -SO 3 H with the formation of 9,10-anthraquinone-2,7-disulphonic acid, resulting in a power density exceeding 0.6 W cm -2 with long cycling life. Therefore, through regulating substituent groups, conjugated structures, Coulomb interactions, and the molecular weight, the electrochemical performance of carbonyl electrode materials can be rationally optimized. This review offers fundamental principles and insight into designing advanced carbonyl materials for the electrodes of next-generation rechargeable batteries. © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Latest advances in supercapacitors: from new electrode materials to novel device designs.

Science.gov (United States)

Wang, Faxing; Wu, Xiongwei; Yuan, Xinhai; Liu, Zaichun; Zhang, Yi; Fu, Lijun; Zhu, Yusong; Zhou, Qingming; Wu, Yuping; Huang, Wei

2017-11-13

Notably, many significant breakthroughs for a new generation of supercapacitors have been reported in recent years, related to theoretical understanding, material synthesis and device designs. Herein, we summarize the state-of-the-art progress toward mechanisms, new materials, and novel device designs for supercapacitors. Firstly, fundamental understanding of the mechanism is mainly focused on the relationship between the structural properties of electrode materials and their electrochemical performances based on some in situ characterization techniques and simulations. Secondly, some emerging electrode materials are discussed, including metal-organic frameworks (MOFs), covalent organic frameworks (COFs), MXenes, metal nitrides, black phosphorus, LaMnO 3 , and RbAg 4 I 5 /graphite. Thirdly, the device innovations for the next generation of supercapacitors are provided successively, mainly emphasizing flow supercapacitors, alternating current (AC) line-filtering supercapacitors, redox electrolyte enhanced supercapacitors, metal ion hybrid supercapacitors, micro-supercapacitors (fiber, plane and three-dimensional) and multifunctional supercapacitors including electrochromic supercapacitors, self-healing supercapacitors, piezoelectric supercapacitors, shape-memory supercapacitors, thermal self-protective supercapacitors, thermal self-charging supercapacitors, and photo self-charging supercapacitors. Finally, the future developments and key technical challenges are highlighted regarding further research in this thriving field.

The use of selective electrodes for the control of nuclear materials

International Nuclear Information System (INIS)

Pires, M.A.F.; Abrao, A.

1984-01-01

The use of ion selective electrodes is discussed for the determination of nitrate, chloride and fluoride in several materials used in the fuel cycle. The determination of nitrate and chloride in thorium compounds, the analysis of fluoride and chloride in uranium compounds and the determination of fluoride in crude phosphoric acid are described. The control of fluoride in urine of individuals that handle materials containing fluor and its compounds is also described. (C.L.B.) [pt

Integration of Microchip Electrophoresis with Electrochemical Detection Using an Epoxy-Based Molding Method to Embed Multiple Electrode Materials

Science.gov (United States)

Johnson, Alicia S.; Selimovic, Asmira; Martin, R. Scott

2012-01-01

This paper describes the use of epoxy-encapsulated electrodes to integrate microchip-based electrophoresis with electrochemical detection. Devices with various electrode combinations can easily be developed. This includes a palladium decoupler with a downstream working electrode material of either gold, mercury/gold, platinum, glassy carbon, or a carbon fiber bundle. Additional device components such as the platinum wires for the electrophoresis separation and the counter electrode for detection can also be integrated into the epoxy base. The effect of the decoupler configuration was studied in terms of the separation performance, detector noise, and the ability to analyze samples of a high ionic strength. The ability of both glassy carbon and carbon fiber bundle electrodes to analyze a complex mixture was demonstrated. It was also shown that a PDMS-based valving microchip can be used along with the epoxy embedded electrodes to integrate microdialysis sampling with microchip electrophoresis and electrochemical detection, with the microdialysis tubing also being embedded in the epoxy substrate. This approach enables one to vary the detection electrode material as desired in a manner where the electrodes can be polished and modified in a similar fashion to electrochemical flow cells used in liquid chromatography. PMID:22038707

Interconnecting Carbon Fibers with the In-situ Electrochemically Exfoliated Graphene as Advanced Binder-free Electrode Materials for Flexible Supercapacitor.

Science.gov (United States)

Zou, Yuqin; Wang, Shuangyin

2015-07-07

Flexible energy storage devices are highly demanded for various applications. Carbon cloth (CC) woven by carbon fibers (CFs) is typically used as electrode or current collector for flexible devices. The low surface area of CC and the presence of big gaps (ca. micro-size) between individual CFs lead to poor performance. Herein, we interconnect individual CFs through the in-situ exfoliated graphene with high surface area by the electrochemical intercalation method. The interconnected CFs are used as both current collector and electrode materials for flexible supercapacitors, in which the in-situ exfoliated graphene act as active materials and conductive "binders". The in-situ electrochemical intercalation technique ensures the low contact resistance between electrode (graphene) and current collector (carbon cloth) with enhanced conductivity. The as-prepared electrode materials show significantly improved performance for flexible supercapacitors.

Carbon nanotube-coated macroporous sponge for microbial fuel cell electrodes

KAUST Repository

Xie, Xing; Ye, Meng; Hu, Liangbing; Liu, Nian; McDonough, James R.; Chen, Wei; Alshareef, Husam N.; Criddle, Craig S.; Cui, Yi

2012-01-01

The materials that are used to make electrodes and their internal structures significantly affect microbial fuel cell (MFC) performance. In this study, we describe a carbon nanotube (CNT)-sponge composite prepared by coating a sponge with CNTs

Nanostructured Electrode Materials for Electrochemical Capacitor Applications

Directory of Open Access Journals (Sweden)

Hojin Choi

2015-06-01

Full Text Available The advent of novel organic and inorganic nanomaterials in recent years, particularly nanostructured carbons, conducting polymers, and metal oxides, has enabled the fabrication of various energy devices with enhanced performance. In this paper, we review in detail different nanomaterials used in the fabrication of electrochemical capacitor electrodes and also give a brief overview of electric double-layer capacitors, pseudocapacitors, and hybrid capacitors. From a materials point of view, the latest trends in electrochemical capacitor research are also discussed through extensive analysis of the literature and by highlighting notable research examples (published mostly since 2013. Finally, a perspective on next-generation capacitor technology is also given, including the challenges that lie ahead.

Edge-riched graphene nanoribbon for high capacity electrode materials

International Nuclear Information System (INIS)

Ping, Yunjie; Zhang, Yupeng; Gong, Youning; Cao, Bing; Fu, Qiang; Pan, Chunxu

2017-01-01

Highlights: •The graphene nanoribbon has been successfully synthesized by longitudinal unzipping of carbon nanotubes with oxidants KMnO 4 . •Compared with graphene oxide and carbon nanotubes, graphene nanoribbon shows the largest capacitance up to ∼202F/g at a scan rate of 5 mV/s. •The importance of the location of functional groups and the importance of the edge structure. •The pseudo-capacitance material should have high electron transfer and rapid ion diffusion. -- Abstract: Carbon materials have attracted great attention for their diversified applications in supercapacitors, and different structures of carbon have been reported to exhibit dissimilar electrochemical properties. In the past, activated carbons, carbon nanotubes (CNTs), carbon nanofibers and graphene have been shown to have excellent electrochemical performances, but it still remains a problem on how to improve the capacitance of carbon-based materials effectively from the viewpoint of their giant commercial potential. Noticing that connecting chemical groups to carbon can provide large pseudo-capacitance, we hereby demonstrated that the position of the chemical groups also plays an important role in the pseudo-capacitance. In our work, we synthesized graphene nanoribbon (GNR), graphene oxide (GO) and functional MWCNTs and showed that GNR has larger capacitance (calculated to be 202 F/g at a scan rate of 5 mV/s) and energy density compared to CNTs and GO when using as electrode materials. Furthermore, the supercapacitor device based on as-synthesized GNR exhibits excellent cycle stability and rate capability which evident is potential in high performance supercapacitor. Revealing the source of the capacitance, we found that though GNR has less oxygen-containing groups, it has larger pseudo-capacitance than GO and CNTs due to the remarkable edge-riched structure with high activity in electrochemical reactions. This finding highlights the importance of edge structure in carbon-based pseudo

Rubber-based carbon electrode materials derived from dumped tires for efficient sodium-ion storage.

Science.gov (United States)

Wu, Zhen-Yue; Ma, Chao; Bai, Yu-Lin; Liu, Yu-Si; Wang, Shi-Feng; Wei, Xiao; Wang, Kai-Xue; Chen, Jie-Sheng

2018-04-03

The development of sustainable and low cost electrode materials for sodium-ion batteries has attracted considerable attention. In this work, a carbon composite material decorated with in situ generated ZnS nanoparticles has been prepared via a simple pyrolysis of the rubber powder from dumped tires. Upon being used as an anode material for sodium-ion batteries, the carbon composite shows a high reversible capacity and rate capability. A capacity as high as 267 mA h g-1 is still retained after 100 cycles at a current density of 50 mA g-1. The well dispersed ZnS nanoparticles in carbon significantly enhance the electrochemical performance. The carbon composites derived from the rubber powder are proposed as promising electrode materials for low-cost, large-scale energy storage devices. This work provides a new and effective method for the reuse of dumped tires, contributing to the recycling of valuable waste resources.

Recent advancements in the cobalt oxides, manganese oxides and their composite as an electrode material for supercapacitor: a review

Science.gov (United States)

Uke, Santosh J.; Akhare, Vijay P.; Bambole, Devidas R.; Bodade, Anjali B.; Chaudhari, Gajanan N.

2017-08-01

In this smart edge, there is an intense demand of portable electronic devices such as mobile phones, laptops, smart watches etc. That demands the use of such components which has light weight, flexible, cheap and environmental friendly. So that needs an evolution in technology. Supercapacitors are energy storage devices emerging as one of the promising energy storage devices in the future energy technology. Electrode material is the important part of supercapacitor. There is much new advancement in types of electrode materials as for supercapacitor. In this review, we focused on the recent advancements in the cobalt oxides, manganese oxides and their composites as an electrodes material for supercapacitor.

Hierarchical structured Sm2O3 modified CuO nanoflowers as electrode materials for high performance supercapacitors

Science.gov (United States)

Zhang, Xiaojuan; He, Mingqian; He, Ping; Liu, Hongtao; Bai, Hongmei; Chen, Jingchao; He, Shaoying; Zhang, Xingquan; Dong, Faqing; Chen, Yang

2017-12-01

By a simple and cost effective chemical precipitation-hydrothermal method, novel hierarchical structured Sm2O3 modified CuO nanoflowers are prepared and investigated as electrode materials for supercapacitors. The physical properties of prepared materials are characterized by XRD, FE-SEM, EDX and FTIR techniques. Furthermore, electrochemical performances of prepared materials are investigated by cyclic voltammetry, galvanostatic charge/discharge and electrochemical impedance spectrum in 1.0 M KOH electrolyte. The resulting Sm2O3 modified CuO based electrodes exhibit obviously enhanced capacitive properties owing to the unique nanostructures and strong synergistic effects. It is worth noting that the optimized SC-3 based electrode exhibits the best electrochemical performances in all prepared electrodes, including higher specific capacitance (383.4 F g-1 at 0.5 A g-1) and good rate capability (393.2 F g-1 and 246.3 F g-1 at 0.3 A g-1 and 3.0 A g-1, respectively), as well as excellent cycling stability (84.6% capacitance retention after 2000 cycles at 1.0 A g-1). The present results show that Sm2O3 is used as a promising modifier to change the morphology and improve electrochemical performances of CuO materials.

Synthesis and electrochemical characterization of Ni-B/ZIF-8 as electrode materials for supercapacitors

Science.gov (United States)

Li, Zhen; Gao, Yilong; Wu, Jianxiang; Zhang, Wei; Tan, Yueyue; Tang, Bohejin

2016-09-01

Ni-B/Zeolitic Imidazolate Frameworks-8 (Ni-B/ZIF-8) is synthesized via a series of solvothermal, incipient wetness impregnation and chemical reduction methods. The ZIF-8 serves as the host for the growth of Ni-B forming a Ni-B/ZIF-8 composite. Characterization by X-ray diffraction and Transmission electron microscope reveals the dispersion of Ni-B in ZIF-8. As electrode materials for supercapacitors, ZIF-8, Ni-B and Ni-B/ZIF-8 electrodes exhibit specific capacitances of 147, 563 and 866 F g-1, respectively at a scan rate of 5 mV s-1 and good stability over 500 cycles. In particular, Ni-B/ZIF-8 is a promising material for supercapacitors.

Cooperation of micro- and meso-porous carbon electrode materials in electric double-layer capacitors

Energy Technology Data Exchange (ETDEWEB)

Zheng, Cheng [State Key Laboratory of Electroanalytical Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, 5625 Renmin Street, Changchun 130022, Jilin Province (China); Graduate University of Chinese Academy of Sciences, Beijing 100039 (China); Qi, Li; Wang, Hongyu [State Key Laboratory of Electroanalytical Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, 5625 Renmin Street, Changchun 130022, Jilin Province (China); Yoshio, Masaki [Advanced Research Center, Saga University, 1341 Yoga-machi, Saga 840-0047 (Japan)

2010-07-01

The capacitive characteristics of micro- and meso-porous carbon materials have been compared in cyclic voltammetric studies and galvanostatic charge-discharge tests. Meso-porous carbon can keep certain high capacitance values at high scan rates, whereas micro-porous carbon possesses very high capacitance values at low scan rates but fades quickly as the scan rate rises up. For better performance of electric double-layer capacitors (EDLCs), the cooperative application of both kinds of carbon materials has been proposed in the following two ways: mixing both kinds of carbons in the same electrode or using the asymmetric configuration of carbon electrodes in the same EDLC. The cooperative effect on the electrochemical performance has also been addressed. (author)

Electrode Materials, Thermal Annealing Sequences, and Lateral/Vertical Phase Separation of Polymer Solar Cells from Multiscale Molecular Simulations

KAUST Repository

Lee, Cheng-Kuang

2014-12-10

© 2014 American Chemical Society. The nanomorphologies of the bulk heterojunction (BHJ) layer of polymer solar cells are extremely sensitive to the electrode materials and thermal annealing conditions. In this work, the correlations of electrode materials, thermal annealing sequences, and resultant BHJ nanomorphological details of P3HT:PCBM BHJ polymer solar cell are studied by a series of large-scale, coarse-grained (CG) molecular simulations of system comprised of PEDOT:PSS/P3HT:PCBM/Al layers. Simulations are performed for various configurations of electrode materials as well as processing temperature. The complex CG molecular data are characterized using a novel extension of our graph-based framework to quantify morphology and establish a link between morphology and processing conditions. Our analysis indicates that vertical phase segregation of P3HT:PCBM blend strongly depends on the electrode material and thermal annealing schedule. A thin P3HT-rich film is formed on the top, regardless of bottom electrode material, when the BHJ layer is exposed to the free surface during thermal annealing. In addition, preferential segregation of P3HT chains and PCBM molecules toward PEDOT:PSS and Al electrodes, respectively, is observed. Detailed morphology analysis indicated that, surprisingly, vertical phase segregation does not affect the connectivity of donor/acceptor domains with respective electrodes. However, the formation of P3HT/PCBM depletion zones next to the P3HT/PCBM-rich zones can be a potential bottleneck for electron/hole transport due to increase in transport pathway length. Analysis in terms of fraction of intra- and interchain charge transports revealed that processing schedule affects the average vertical orientation of polymer chains, which may be crucial for enhanced charge transport, nongeminate recombination, and charge collection. The present study establishes a more detailed link between processing and morphology by combining multiscale molecular

Influence of carbon electrode material on energy recovery from winery wastewater using a dual-chamber microbial fuel cell.

Science.gov (United States)

Penteado, Eduardo D; Fernandez-Marchante, Carmen M; Zaiat, Marcelo; Gonzalez, Ernesto R; Rodrigo, Manuel A

2017-06-01

The aim of this work was to evaluate three carbon materials as anodes in microbial fuel cells (MFCs), clarifying their influence on the generation of electricity and on the treatability of winery wastewater, a highly organic-loaded waste. The electrode materials tested were carbon felt, carbon cloth and carbon paper and they were used at the same time as anode and cathode in the tests. The MFC equipped with carbon felt reached the highest voltage and power (72 mV and 420 mW m -2 , respectively), while the lowest values were observed when carbon paper was used as electrode (0.2 mV and 8.37·10 -6  mW m -2 , respectively). Chemical oxygen demand (COD) removal from the wastewater was observed to depend on the electrode material, as well. When carbon felt was used, the MFC showed the highest average organic matter consumption rate (650 mg COD L -1  d -1 ), whereas by using carbon paper the rate decreased to 270 mg COD L -1  d -1 . Therefore, both electricity generation and organic matter removal are strongly related not to the chemical composition of the electrode (which was graphite carbon in the three electrodes), but to its surface features and, consequently, to the amount of biomass adhered to the electrode surface.

Carbonized chicken eggshell membranes with 3D architectures as high-performance electrode materials for supercapacitors

Energy Technology Data Exchange (ETDEWEB)

Li, Zhi; Zhang, Li; Amirkhiz, Babak Shalchi; Tan, Xuehai; Xu, Zhanwei; Wang, Huanlei; Olsen, Brian C.; Holt, Chris M.B.; Mitlin, David [Chemical and Materials Engineering, University of Alberta, Edmonton, AB (Canada); National Institute for Nanotechnology (NINT), NRC, Edmonton, AB (Canada)

2012-04-15

Supercapacitor electrode materials are synthesized by carbonizing a common livestock biowaste in the form of chicken eggshell membranes. The carbonized eggshell membrane (CESM) is a three-dimensional macroporous carbon film composed of interwoven connected carbon fibers containing around 10 wt% oxygen and 8 wt% nitrogen. Despite a relatively low surface area of 221 m{sup 2} g{sup -1}, exceptional specific capacitances of 297 F g{sup -1} and 284 F g{sup -1} are achieved in basic and acidic electrolytes, respectively, in a 3-electrode system. Furthermore, the electrodes demonstrate excellent cycling stability: only 3% capacitance fading is observed after 10 000 cycles at a current density of 4 A g{sup -1}. These very attractive electrochemical properties are discussed in the context of the unique structure and chemistry of the material. (Copyright copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

Speci﬿c contact resistance of phase change materials to metal electrode

NARCIS (Netherlands)

Roy, Deepu; in 't Zandt, Micha A.A.; Wolters, Robertus A.M.

2010-01-01

For phase change random access memory (PCRAM) cells, it is important to know the contact resistance of phase change materials (PCMs) to metal electrodes at the contacts. In this letter, we report the systematic determination of the speci﬿c contact resistance (Ͽc ) of doped Sb2Te and Ge2Sb2Te5 to TiW

Niobium Nitride Nb4N5 as a New High-Performance Electrode Material for Supercapacitors.

Science.gov (United States)

Cui, Houlei; Zhu, Guilian; Liu, Xiangye; Liu, Fengxin; Xie, Yian; Yang, Chongyin; Lin, Tianquan; Gu, Hui; Huang, Fuqiang

2015-12-01

Supercapacitors suffer either from low capacitance for carbon or derivate electrodes or from poor electrical conductivity and electrochemical stability for metal oxide or conducting polymer electrodes. Transition metal nitrides possess fair electrical conductivity but superior chemical stability, which may be desirable candidates for supercapacitors. Herein, niobium nitride, Nb 4 N 5 , is explored to be an excellent capacitive material for the first time. An areal capacitance of 225.8 mF cm -2 , with a reasonable rate capability (60.8% retention from 0.5 to 10 mA cm -2 ) and cycling stability (70.9% retention after 2000 cycles), is achieved in Nb 4 N 5 nanochannels electrode with prominent electrical conductivity and electrochemical activity. Faradaic pseudocapacitance is confirmed by the mechanistic studies, deriving from the proton incorporation/chemisorption reaction owing to the copious +5 valence Nb ions in Nb 4 N 5 . Moreover, this Nb 4 N 5 nanochannels electrode with an ultrathin carbon coating exhibits nearly 100% capacitance retention after 2000 CV cycles, which is an excellent cycling stability for metal nitride materials. Thus, the Nb 4 N 5 nanochannels are qualified for a candidate for supercapacitors and other energy storage applications.

Niobium Nitride Nb4N5 as a New High‐Performance Electrode Material for Supercapacitors

Science.gov (United States)

Cui, Houlei; Zhu, Guilian; Liu, Xiangye; Liu, Fengxin; Xie, Yian; Yang, Chongyin; Lin, Tianquan; Gu, Hui

2015-01-01

Supercapacitors suffer either from low capacitance for carbon or derivate electrodes or from poor electrical conductivity and electrochemical stability for metal oxide or conducting polymer electrodes. Transition metal nitrides possess fair electrical conductivity but superior chemical stability, which may be desirable candidates for supercapacitors. Herein, niobium nitride, Nb4N5, is explored to be an excellent capacitive material for the first time. An areal capacitance of 225.8 mF cm−2, with a reasonable rate capability (60.8% retention from 0.5 to 10 mA cm−2) and cycling stability (70.9% retention after 2000 cycles), is achieved in Nb4N5 nanochannels electrode with prominent electrical conductivity and electrochemical activity. Faradaic pseudocapacitance is confirmed by the mechanistic studies, deriving from the proton incorporation/chemisorption reaction owing to the copious +5 valence Nb ions in Nb4N5. Moreover, this Nb4N5 nanochannels electrode with an ultrathin carbon coating exhibits nearly 100% capacitance retention after 2000 CV cycles, which is an excellent cycling stability for metal nitride materials. Thus, the Nb4N5 nanochannels are qualified for a candidate for supercapacitors and other energy storage applications. PMID:27980920

Effective dose in the manufacturing process of rutile covered welding electrodes.

Science.gov (United States)

Herranz, M; Rozas, S; Pérez, C; Idoeta, R; Núñez-Lagos, R; Legarda, F

2013-03-01

Shielded metal arc welding using covered electrodes is the most common welding process. Sometimes the covering contains naturally occurring radioactive materials (NORMs). In Spain the most used electrodes are those covered with rutile mixed with other materials. Rutile contains some detectable natural radionuclides, so it can be considered a NORM. This paper mainly focuses on the use of MCNP (Monte Carlo N-Particle Transport Code) as a predictive tool to obtain doses in a factory which produces this type of electrode and assess the radiological impact in a specific facility after estimating the internal dose.To do this, in the facility, areas of highest radiation and positions of workers were identified, radioactive content of rutile and rutile covered electrodes was measured, and, considering a worst possible scenario, external dose at working points has been calculated using MCNP. This procedure has been validated comparing the results obtained with those from a pressurised ionisation chamber and TLD dosimeters. The internal dose has been calculated using DCAL (dose and risk calculation). The doses range between 8.8 and 394 μSv yr(-1), always lower than the effective dose limit for the public, 1 mSv yr(-1). The highest dose corresponds to the mixing area.

Potential electrode materials for symmetrical Solid Oxide Fuel Cells

Directory of Open Access Journals (Sweden)

Ruiz Morales, J. C.

2008-08-01

Full Text Available Chromites, titanates and Pt-YSZ-CeO₂ cermets have been investigated as potential electrode materials for an alternative concept of Solid Oxide Fuel Cell (SOFC, the symmetrical SOFCs (SFC. In this configuration, the same electrode material is used simultaneously as anode and cathode. Interconnector materials, such as chromites, could be considered as potential SFC electrodes, at least under pure hydrogen-fed at relatively high temperatures, as they do not exhibit significant catalytic activity towards hydrocarbon oxidation. This may be overcome by partially substituting Cr in the perovskite B-sites by other transition metal cations such as Mn. La_0.75Sr_0.25Cr_0.5Mn_0.5O_3-δ (LSCM is a good candidate for such SFCs, rendering fuel cell performances in excess of 500 and 300mW/cm² using pure H₂ and CH₄ as fuel, at 950 ^oC. Similarly, typical n-type electronic conductors traditionally regarded as anode materials, such as strontium titanates, may also operate under oxidising conditions as cathodes by substituting some Ti content for Fe to introduce p-type conductivity. Preliminary electrochemical experiments on La₄Sr₈Ti_12-xFe_xO_38-δ-based SFCs show that they perform reasonably well under humidified H₂, at high temperatures. A third group of materials is the support material of any typical cermet anode, i.e. YSZ, CeO₂ plus a current collector. It has been found that this combination could be optimised to operate as SFC electrodes, rendering performances of 400mW/cm² under humidified pure H₂ at 950^oC.

Cromitas, titanatos y cermets de Pt-YSZ-CeO₂ han sido investigados como potenciales materiales de electrodo para un concepto alternativo de Pilas de Combustible de Óxidos Sólidos (SOFC, las pilas SOFC simétricas (SFC. En

Nanostructured MnO₂ as Electrode Materials for Energy Storage.

Science.gov (United States)

Julien, Christian M; Mauger, Alain

2017-11-17

Manganese dioxides, inorganic materials which have been used in industry for more than a century, now find great renewal of interest for storage and conversion of energy applications. In this review article, we report the properties of MnO₂ nanomaterials with different morphologies. Techniques used for the synthesis, structural, physical properties, and electrochemical performances of periodic and aperiodic frameworks are discussed. The effect of the morphology of nanosized MnO₂ particles on their fundamental features is evidenced. Applications as electrodes in lithium batteries and supercapacitors are examined.

Graphene/MnO{sub 2} hybrid nanosheets as high performance electrode materials for supercapacitors

Energy Technology Data Exchange (ETDEWEB)

Mondal, Anjon Kumar, E-mail: Anjon.K.Mondal@student.uts.edu.au [Centre for Clean Energy Technology, School of Chemistry and Forensic Science, University of Technology, Sydney, Broadway, Sydney, NSW 2007 (Australia); Wang, Bei; Su, Dawei; Wang, Ying; Chen, Shuangqiang [Centre for Clean Energy Technology, School of Chemistry and Forensic Science, University of Technology, Sydney, Broadway, Sydney, NSW 2007 (Australia); Zhang, Xiaogang [College of Materials Science and Engineering, Nanjing University of Aeronautics and Astronautics, Nanjing (China); Wang, Guoxiu, E-mail: Guoxiu.wang@uts.edu.au [Centre for Clean Energy Technology, School of Chemistry and Forensic Science, University of Technology, Sydney, Broadway, Sydney, NSW 2007 (Australia)

2014-01-15

Graphene/MnO{sub 2} hybrid nanosheets were prepared by incorporating graphene and MnO{sub 2} nanosheets in ethylene glycol. Scanning electron microscopy and transmission electron microscopy analyses confirmed nanosheet morphology of the hybrid materials. Graphene/MnO{sub 2} hybrid nanosheets with different ratios were investigated as electrode materials for supercapacitors by cyclic voltammetry (CV) and galvanostatic charge–discharge in 1 M Na{sub 2}SO{sub 4} electrolyte. We found that the graphene/MnO{sub 2} hybrid nanosheets with a weight ratio of 1:4 (graphene:MnO{sub 2}) delivered the highest specific capacitance of 320 F g{sup −1}. Graphene/MnO{sub 2} hybrid nanosheets also exhibited good capacitance retention on 2000 cycles. - Highlights: • Graphene/MnO{sub 2} hybrid nanosheets with different ratios were fabricated. • The specific capacitance is strongly dependent on graphene/MnO{sub 2} ratios. • The graphene/MnO{sub 2} hybrid electrode (1:4) exhibited high specific capacitance. • The electrode retained 84% of the initial specific capacitance after 2000 cycles.

Recent Advancements in the Cobalt Oxides, Manganese Oxides, and Their Composite As an Electrode Material for Supercapacitor: A Review

Directory of Open Access Journals (Sweden)

Santosh J. Uke

2017-08-01

Full Text Available Recently, our modern society demands the portable electronic devices such as mobile phones, laptops, smart watches, etc. Such devices demand light weight, flexible, and low-cost energy storage systems. Among different energy storage systems, supercapacitor has been considered as one of the most potential energy storage systems. This has several significant merits such as high power density, light weight, eco-friendly, etc. The electrode material is the important part of the supercapacitor. Recent studies have shown that there are many new advancement in electrode materials for supercapacitors. In this review, we focused on the recent advancements in the cobalt oxides, manganese oxides, and their composites as an electrode material for supercapacitor.

Operando XRD studies as a tool for determination of transport parameters of mobile ions in electrode materials

Science.gov (United States)

Kondracki, Łukasz; Kulka, Andrzej; Świerczek, Konrad; Ziąbka, Magdalena; Molenda, Janina

2017-11-01

In this work a detailed operando XRD investigations of structural properties of LixMn2O4 manganese spinel are shown to be a complementary, successful method of determination of diffusion coefficient D and surface exchange coefficient k in the working electrode. Kinetics of lithium ions transport are estimated on the basis of rate of structural changes of the cathode material during a relaxation stage after a high current charge, i.e. during structural relaxation of the material. The presented approach seems to be applicable as a complementary method of determination of transport coefficients for all intercalation-type electrode materials.

Synthesis of nitrogen-doped porous carbon nanofibers as an efficient electrode material for supercapacitors.

Science.gov (United States)

Chen, Li-Feng; Zhang, Xu-Dong; Liang, Hai-Wei; Kong, Mingguang; Guan, Qing-Fang; Chen, Ping; Wu, Zhen-Yu; Yu, Shu-Hong

2012-08-28

Supercapacitors (also known as ultracapacitors) are considered to be the most promising approach to meet the pressing requirements of energy storage. Supercapacitive electrode materials, which are closely related to the high-efficiency storage of energy, have provoked more interest. Herein, we present a high-capacity supercapacitor material based on the nitrogen-doped porous carbon nanofibers synthesized by carbonization of macroscopic-scale carbonaceous nanofibers (CNFs) coated with polypyrrole (CNFs@polypyrrole) at an appropriate temperature. The composite nanofibers exhibit a reversible specific capacitance of 202.0 F g(-1) at the current density of 1.0 A g(-1) in 6.0 mol L(-1) aqueous KOH electrolyte, meanwhile maintaining a high-class capacitance retention capability and a maximum power density of 89.57 kW kg(-1). This kind of nitrogen-doped carbon nanofiber represents an alternative promising candidate for an efficient electrode material for supercapacitors.

Graphene-Wrapped Ni(OH)2 Hollow Spheres as Novel Electrode Material for Supercapacitors.

Science.gov (United States)

Sun, Jinfeng; Wang, Jinqing; Li, Zhangpeng; Ou, Junfei; Niu, Lengyuan; Wang, Honggang; Yang, Shengrong

2015-09-01

Graphene-wrapped Ni(OH)2 hollow spheres were prepared via electrostatic interaction between poly(diallyldimethylammonium chloride) (PDDA) modified Ni(OH)2 and graphene oxide (GO) in an aqueous dispersion, followed by the reduction of GO. Morphological and structural analysis by field-emission scanning electron microscopy, X-ray diffraction, Raman spectroscopy, X-ray photoelectron spectroscopy and thermogravimetric analysis confirmed the successful coating of graphene on Ni(OH)2 hollow spheres with a content of 3.8 wt%. And then its application as electrode material for supercapacitor has been investigated by cyclic voltammetry (CV) and galvanostatic charge-discharge tests. Results show that the sample displays a high capacitance of 1368 F g(-1) at a current density of 1 A g(-1), much better than that of pure Ni(OH)2, illustrating that such composite is a promising candidate as electrode material for supercapacitors.

Robust high temperature oxygen sensor electrodes

DEFF Research Database (Denmark)

Lund, Anders

Platinum is the most widely used material in high temperature oxygen sensor electrodes. However, platinum is expensive and the platinum electrode may, under certain conditions, suffer from poisoning, which is detrimental for an oxygen sensor. The objective of this thesis is to evaluate electrode...... materials as candidates for robust oxygen sensor electrodes. The present work focuses on characterising the electrochemical properties of a few electrode materials to understand which oxygen electrode processes are limiting for the response time of the sensor electrode. Three types of porous platinum......-Dansensor. The electrochemical properties of the electrodes were characterised by electrochemical impedance spectroscopy (EIS), and the structures were characterised by x-ray diffraction and electron microscopy. At an oxygen partial pressures of 0.2 bar, the response time of the sensor electrode was determined by oxygen...

Nitrogen-doped carbon based on peptides of hair as electrode materials for surpercapacitors

International Nuclear Information System (INIS)

Guo, Zihan; Zhou, Qingwen; Wu, Zhaojun; Zhang, Zhiguo; Zhang, Wen; Zhang, Yao; Li, Lijun; Cao, Zhenzhu; Wang, Hong; Gao, Yanfang

2013-01-01

Highlights: • Hair was directly carbonized by environmental and energy-saving methods. • Hair was utilized to prepare nitrogen-doped carbon materials for supercapacitor. • A new approache for preparing nitrogen-rich active carbon from biomass waste of hair-like precursor. • Hair-based carbon having a non-crystalline layered structure and excellent capacitive performance. -- Abstract: Hair, a high-nitrogen energetic material, is utilized as a precursor for nitrogen-doped porous carbon. The preparation procedures for obtaining carbon from hair are very simple, namely, reductant or deionized water activation process followed by hair carbonization under argon atmosphere at 800 °C for 2 h. The samples are characterized through scanning electron microscopy, transmission electron microscopy, X-ray diffraction, nitrogen adsorption, and X-ray photoelectron microscopy. The carbon samples are tested as electrode materials in supercapacitors in a three-electrode system. The carbon (soaked in deionized water at 80 °C) presents relatively low specific surface areas (441.34 m 2 g −1 ) and shows higher capacitance (154.5 F g −1 ) compared with nitrogen-free commercial activated carbons (134.5 F g −1 ) at 5 A g −1 . The capacitance remains at 130.5 F g −1 even when the current load is increased to 15 A g −1 . The capacitance loss is only 5% in 6 M KOH after 10,000 charge and discharge cycles at 5 A g −1 . It is the unique microstructure after activation processing and electroactive nitrogen functionalities that enable the carbon obtained through a simple, ecological, and economical process to be utilized as a potential electrode material for electrical double-layer capacitors

Recent Advances in Polymeric Materials Used as Electron Mediators and Immobilizing Matrices in Developing Enzyme Electrodes

Directory of Open Access Journals (Sweden)

Mambo Moyo

2012-01-01

Full Text Available Different classes of polymeric materials such as nanomaterials, sol-gel materials, conducting polymers, functional polymers and biomaterials have been used in the design of sensors and biosensors. Various methods have been used, for example from direct adsorption, covalent bonding, crossing-linking with glutaraldehyde on composites to mixing the enzymes or use of functionalized beads for the design of sensors and biosensors using these polymeric materials in recent years. It is widely acknowledged that analytical sensing at electrodes modified with polymeric materials results in low detection limits, high sensitivities, lower applied potential, good stability, efficient electron transfer and easier immobilization of enzymes on electrodes such that sensing and biosensing of environmental pollutants is made easier. However, there are a number of challenges to be addressed in order to fulfill the applications of polymeric based polymers such as cost and shortening the long laboratory synthetic pathways involved in sensor preparation. Furthermore, the toxicological effects on flora and fauna of some of these polymeric materials have not been well studied. Given these disadvantages, efforts are now geared towards introducing low cost biomaterials that can serve as alternatives for the development of novel electrochemical sensors and biosensors. This review highlights recent contributions in the development of the electrochemical sensors and biosensors based on different polymeric material. The synergistic action of some of these polymeric materials and nanocomposites imposed when combined on electrode during sensing is discussed.

Few-layer MoS2-anchored graphene aerogel paper for free-standing electrode materials.

Science.gov (United States)

Lee, Wee Siang Vincent; Peng, Erwin; Loh, Tamie Ai Jia; Huang, Xiaolei; Xue, Jun Min

2016-04-21

To reduce the reliance on polymeric binders, conductive additives, and metallic current collectors during the electrode preparation process, as well as to assess the true performance of lithium ion battery (LIB) anodes, a free-standing electrode has to be meticulously designed. Graphene aerogel is a popular scaffolding material that has been widely used with embedded nanoparticles for application in LIB anodes. However, the current graphene aerogel/nanoparticle composite systems still involve decomposition into powder and the addition of additives during electrode preparation because of the thick aerogel structure. To further enhance the capacity of the system, MoS2 was anchored onto a graphene aerogel paper and the composite was used directly as an LIB anode. The resultant additive-free MoS2/graphene aerogel paper composite exhibited long cyclic performance with 101.1% retention after 700 cycles, which demonstrates the importance of free-standing electrodes in enhancing cyclic stability.

The preparation and performance of calcium carbide-derived carbon/polyaniline composite electrode material for supercapacitors

Energy Technology Data Exchange (ETDEWEB)

Zheng, Liping; Wang, Xianyou; Li, Na; An, Hongfang; Chen, Huajie [School of Chemistry, Key Laboratory of Environmentally Friendly Chemistry and Applications of Minister of Education, Xiangtan University, Hunan 411105 (China); Wang, Ying; Guo, Jia [School of Chemical Engineering and Pharmacy, Wuhan Institute of Technology, Hubei 430073 (China)

2010-03-15

Calcium carbide (CaC{sub 2})-derived carbon (CCDC)/polyaniline (PANI) composite materials are prepared by in situ chemical oxidation polymerization of an aniline solution containing well-dispersed CCDC. The structure and morphology of CCDC/PANI composite are characterized by Fourier infrared spectroscopy (FTIR), scanning electron microscope (SEM), transmission electron microscopy (TEM) and N{sub 2} sorption isotherms. It has been found that PANI was uniformly deposited on the surface and the inner pores of CCDC. The supercapacitive behaviors of the CCDC/PANI composite materials are investigated with cyclic voltammetry (CV), galvanostatic charge/discharge and cycle life measurements. The results show that the CCDC/PANI composite electrodes have higher specific capacitances than the as grown CCDC electrodes and higher stability than the conducting polymers. The capacitance of CCDC/PANI composite electrode is as high as 713.4 F g{sup -1} measured by cyclic voltammetry at 1 mV s{sup -1}. Besides, the capacitance retention of coin supercapacitor remained 80.1% after 1000 cycles. (author)

Chitin based heteroatom-doped porous carbon as electrode materials for supercapacitors.

Science.gov (United States)

Zhou, Jie; Bao, Li; Wu, Shengji; Yang, Wei; Wang, Hui

2017-10-01

Chitin biomass has received much attention as an amino-functional polysaccharide precursor for synthesis of carbon materials. Rich nitrogen and oxygen dual-doped porous carbon derived from cicada slough (CS), a renewable biomass mainly composed of chitin, was synthesized and employed as electrode materials for electrochemical capacitors, for the first time ever. The cicada slough-derived carbon (CSC) was prepared by a facile process via pre-carbonization in air, followed by KOH activation. The weight ratio of KOH and char plays an important role in fabricating the microporous structure and tuning the surface chemistry of CSC. The obtained CSC had a large specific surface area (1243-2217m 2 g -1 ), fairly high oxygen content (28.95-33.78 at%) and moderate nitrogen content (1.47-4.35 at%). The electrochemical performance of the CS char and CSC as electrodes for capacitors was evaluated in a three-electrode cell configuration with 6M KOH as the electrolyte. Electrochemical studies showed that the as-prepared CSC activated at the KOH-to-char weight ratio of 2 exhibited the highest specific capacitance (266.5Fg -1 at a current density of 0.5Ag -1 ) and excellent rate capability (196.2Fg -1 remained at 20Ag -1 ) and cycle durability. In addition, the CSC-2-based symmetrical device possessed the desirable energy density and power density of about 15.97Whkg -1 and 5000Wkg -1 at 5Ag -1 , respectively. Copyright © 2017 Elsevier Ltd. All rights reserved.

Carbon nanotube-coated macroporous sponge for microbial fuel cell electrodes

KAUST Repository

Xie, Xing

2012-01-01

The materials that are used to make electrodes and their internal structures significantly affect microbial fuel cell (MFC) performance. In this study, we describe a carbon nanotube (CNT)-sponge composite prepared by coating a sponge with CNTs. Compared to the CNT-coated textile electrodes evaluated in prior studies, CNT-sponge electrodes had lower internal resistance, greater stability, more tunable and uniform macroporous structure (pores up to 1 mm in diameter), and improved mechanical properties. The CNT-sponge composite also provided a three-dimensional scaffold that was favorable for microbial colonization and catalytic decoration. Using a batch-fed H-shaped MFC outfitted with CNT-sponge electrodes, an areal power density of 1.24 W m -2 was achieved when treating domestic wastewater. The maximum volumetric power density of a continuously fed plate-shaped MFC was 182 W m -3. To our knowledge, these are the highest values obtained to date for MFCs fed domestic wastewater: 2.5 times the previously reported maximum areal power density and 12 times the previously reported maximum volumetric power density. © 2011 The Royal Society of Chemistry.

Importance of Electrode Material in the Electrochemical Treatment of Wastewater Containing Organic Pollutants

Science.gov (United States)

Panizza, Marco

Electrochemical oxidation is a promising method for the treatment of wastewaters containing organic compounds. As a general rule, the electrochemical incineration of organics at a given electrode can take place at satisfactory rates and without electrode deactivation only at high anodic potentials in the region of the water discharge due to the participation of the intermediates of oxygen evolution. The nature of the electrode material strongly influences both the selectivity and the efficiency of the process. In particular, anodes with low oxygen evolution overpotential (i.e., good catalysts for oxygen evolution reactions), such as graphite, IrO2, RuO2, and Pt only permit the partial oxidation of organics, while anodes with high oxygen evolution overpotential (i.e., anodes that are poor catalysts for oxygen evolution reactions), such as SnO2, PbO2, and boron-doped diamond (BDD) favor the complete oxidation of organics to CO2 and so are ideal electrodes for wastewater treatment.However, the application of SnO2 and PbO2 anodes may be limited by their short service life and the risk of lead contamination, while BDD electrodes exhibit good chemical and electrochemical stability, a long life, and a wide potential window for water discharge, and are thus promising anodes for industrial-scale wastewater treatment.

The modification of glassy carbon and gold electrodes with aryl diazonium salt: The impact of the electrode materials on the rate of heterogeneous electron transfer

International Nuclear Information System (INIS)

Liu Guozhen; Liu Jingquan; Boecking, Till; Eggers, Paul K.; Gooding, J. Justin

2005-01-01

The heterogeneous electron-transfer properties of ferrocenemethylamine coupled to a series of mixed 4-carboxyphenyl/phenyl monolayers on glassy carbon (GC) and gold electrodes were investigated, by cyclic voltammetry, in aqueous buffer solutions. The electrodes were derivatized in a step-wise process. Electrochemical reduction of mixtures of 4-carboxyphenyl and phenyl diazonium salts on the electrode surfaces yielded stable monolayers. The introduction of carboxylic acid moieties onto the surfaces was verified by X-ray photoelectron spectroscopy. Subsequently the 4-carboxyphenyl moieties were activated using water-soluble carbodiimide and N-hydroxysuccinimide and reacted with ferrocenemethylamine. The rate constants of electron transfer through the monolayer systems were determined from cyclic voltammograms using the Marcus theory for electron transfer and were found to be an order of magnitude higher for the ferrocene-modified monolayer systems on gold than those on GC electrodes. The results suggest the electrode material has an important influence on the rate of electron transfer

Studies on two classes of positive electrode materials for lithium-ion batteries

Energy Technology Data Exchange (ETDEWEB)

Wilcox, James Douglas [Univ. of California, Berkeley, CA (United States)

2008-12-01

The development of advanced lithium-ion batteries is key to the success of many technologies, and in particular, hybrid electric vehicles. In addition to finding materials with higher energy and power densities, improvements in other factors such as cost, toxicity, lifetime, and safety are also required. Lithium transition metal oxide and LiFePO₄/C composite materials offer several distinct advantages in achieving many of these goals and are the focus of this report. Two series of layered lithium transition metal oxides, namely LiNi_1/3Co_1/3-yM_yMn_1/3O₂ (M=Al, Co, Fe, Ti) and LiNi_0.4Co_0.2-yM_yMn_0.4O₂ (M = Al, Co, Fe), have been synthesized. The effect of substitution on the crystal structure is related to shifts in transport properties and ultimately to the electrochemical performance. Partial aluminum substitution creates a high-rate positive electrode material capable of delivering twice the discharge capacity of unsubstituted materials. Iron substituted materials suffer from limited electrochemical performance and poor cycling stability due to the degradation of the layered structure. Titanium substitution creates a very high rate positive electrode material due to a decrease in the anti-site defect concentration. LiFePO₄ is a very promising electrode material but suffers from poor electronic and ionic conductivity. To overcome this, two new techniques have been developed to synthesize high performance LiFePO₄/C composite materials. The use of graphitization catalysts in conjunction with pyromellitic acid leads to a highly graphitic carbon coating on the surface of LiFePO₄ particles. Under the proper conditions, the room temperature electronic conductivity can be improved by nearly five orders of magnitude over untreated materials. Using Raman spectroscopy, the improvement in conductivity and rate performance of

Synthesis and characterization of NiCo{sub 2}O{sub 4} nanoplates as efficient electrode materials for electrochemical supercapacitors

Energy Technology Data Exchange (ETDEWEB)

Kim, Taehyun [Nanomaterials and System Lab, Department of Mechatronics Engineering, Engineering College, Jeju National University, Jeju 690-756 (Korea, Republic of); Ramadoss, Ananthakumar [Nanomaterials and System Lab, Faculty of Applied Energy System, Science and Engineering College, Jeju National University, Jeju 690-756 (Korea, Republic of); Saravanakumar, Balasubramaniam; Veerasubramani, Ganesh Kumar [Nanomaterials and System Lab, Department of Mechatronics Engineering, Engineering College, Jeju National University, Jeju 690-756 (Korea, Republic of); Kim, Sang Jae, E-mail: kimsangj@jejunu.ac.kr [Nanomaterials and System Lab, Department of Mechatronics Engineering, Engineering College, Jeju National University, Jeju 690-756 (Korea, Republic of); Nanomaterials and System Lab, Faculty of Applied Energy System, Science and Engineering College, Jeju National University, Jeju 690-756 (Korea, Republic of)

2016-05-01

Highlights: • NiCo{sub 2}O{sub 4} nanoplates were synthesized through a facile approach. • The NiCo{sub 2}O{sub 4} nanoplates electrode material exhibit a specific capacitance of 332 F g{sup −1} at 5 mV s{sup −1}. • The fabricated NiCo{sub 2}O{sub 4} electrode reveals 86% retention of initial capacitance after 2000 cycles. - Abstract: In the present work, NiCo{sub 2}O{sub 4} nanoplates were prepared by a facile, low temperature, hydrothermal method, followed by thermal annealing and used supercapacitor applications. The physico-chemical characterization of as-prepared materials were investigated by means of X-ray diffraction (XRD), Fourier transform infra-red spectroscopy (FT-IR) and field emission scanning electron microscopy (FE-SEM). The electrochemical measurements demonstrate that the NiCo{sub 2}O{sub 4} nanoplates electrode (NC-5) exhibits a high specific capacitance of 332 F g{sup −1} at a scan rate of 5 mV s{sup −1} and also retained about 86% of the initial specific capacitance value even after 2000 cycles at a current density of 2.5 A g{sup −1}. These results suggest that the fabricated electrode material has huge potential as a novel electrode material for electrochemical capacitors.

Highly Flexible Freestanding Porous Carbon Nanofibers for Electrodes Materials of High-Performance All-Carbon Supercapacitors.

Science.gov (United States)

Liu, Ying; Zhou, Jinyuan; Chen, Lulu; Zhang, Peng; Fu, Wenbin; Zhao, Hao; Ma, Yufang; Pan, Xiaojun; Zhang, Zhenxing; Han, Weihua; Xie, Erqing

2015-10-28

Highly flexible porous carbon nanofibers (P-CNFs) were fabricated by electrospining technique combining with metal ion-assistant acid corrosion process. The resultant fibers display high conductivity and outstanding mechanical flexibility, whereas little change in their resistance can be observed under repeatedly bending, even to 180°. Further results indicate that the improved flexibility of P-CNFs can be due to the high graphitization degree caused by Co ions. In view of electrode materials for high-performance supercapacitors, this type of porous nanostructure and high graphitization degree could synergistically facilitate the electrolyte ion diffusion and electron transportation. In the three electrodes testing system, the resultant P-CNFs electrodes can exhibit a specific capacitance of 104.5 F g(-1) (0.2 A g(-1)), high rate capability (remain 56.5% at 10 A g(-1)), and capacitance retention of ∼94% after 2000 cycles. Furthermore, the assembled symmetric supercapacitors showed a high flexibility and can deliver an energy density of 3.22 Wh kg(-1) at power density of 600 W kg(-1). This work might open a way to improve the mechanical properties of carbon fibers and suggests that this type of freestanding P-CNFs be used as effective electrode materials for flexible all-carbon supercapacitors.

Few-layered CoHPO4 · 3H2O ultrathin nanosheets for high performance of electrode materials for supercapacitors.

Science.gov (United States)

Pang, Huan; Wang, Shaomei; Shao, Weifang; Zhao, Shanshan; Yan, Bo; Li, Xinran; Li, Sujuan; Chen, Jing; Du, Weimin

2013-07-07

Ultrathin cobalt phosphate (CoHPO4 · 3H2O) nanosheets are successfully synthesized by a one pot hydrothermal method. Novel CoHPO4 · 3H2O ultrathin nanosheets are assembled for constructing the electrodes of supercapacitors. Benefiting from the nanostructures, the as-prepared electrode shows a specific capacitance of 413 F g(-1), and no obvious decay even after 3000 charge-discharge cycles. Such a quasi-two-dimensional material is a new kind of supercapacitor electrode material with high performance.

Porous nickel hydroxide-manganese dioxide-reduced graphene oxide ternary hybrid spheres as excellent supercapacitor electrode materials.

Science.gov (United States)

Chen, Hao; Zhou, Shuxue; Wu, Limin

2014-06-11

This paper reports the first nickel hydroxide-manganese dioxide-reduced graphene oxide (Ni(OH)2-MnO2-RGO) ternary hybrid sphere powders as supercapacitor electrode materials. Due to the abundant porous nanostructure, relatively high specific surface area, well-defined spherical morphology, and the synergetic effect of Ni(OH)2, MnO2, and RGO, the electrodes with the as-obtained Ni(OH)2-MnO2-RGO ternary hybrid spheres as active materials exhibited significantly enhanced specific capacitance (1985 F·g(-1)) and energy density (54.0 Wh·kg(-1)), based on the total mass of active materials. In addition, the Ni(OH)2-MnO2-RGO hybrid spheres-based asymmetric supercapacitor also showed satisfying energy density and electrochemical cycling stability.

Nanocomposite of cobalt oxide and ordered mesoporous carbon as the electrode materials for supercapacitor

Energy Technology Data Exchange (ETDEWEB)

Xu, J.; Liu, P.; Zhao, J.; Feng, J.; Tang, B. [Shanghai Univ. of Engineering Science (China). College of Chemistry and Chemical Engineering

2010-07-01

An incipient wetness impregnation method was used to prepare a cobalt oxide ordered mesoporous carbon composite for use as an electrode in supercapacitor applications. The composite was then incorporated inside periodic nanoholes in the ordered mesoporous carbon (OMC). X-ray diffraction (XRD), transmission electron microscopy (TEM) and N{sub 2} adsorption-desorption isotherm analyses were used to characterize the structures of the samples. The specific capacitance of the synthesized materials was estimated using cyclic voltammetric (CV) analyses. The study showed that composites prepared using the new method exhibited a higher reversible specific capacitance of 594.8 F per g at a scan rate of 5 mV per second. The composite also showed good cyclic stability. Results suggested that the composite can be used as an electrode material in supercapacitors.

Template-free synthesis of renewable macroporous carbon via yeast cells for high-performance supercapacitor electrode materials.

Science.gov (United States)

Sun, Hongmei; He, Wenhui; Zong, Chenghua; Lu, Lehui

2013-03-01

The urgent need for sustainable development has forced material scientists to explore novel materials for next-generation energy storage devices through a green and facile strategy. In this context, yeast, which is a large group of single cell fungi widely distributed in nature environments, will be an ideal candidate for developing effective electrode materials with fascinating structures for high-performance supercapacitors. With this in mind, herein, we present the first example of creating three-dimensional (3D) interpenetrating macroporous carbon materials via a template-free method, using the green, renewable, and widespread yeast cells as the precursors. Remarkably, when the as-prepared materials are used as the electrode materials for supercapacitors, they exhibit outstanding performance with high specific capacitance of 330 F g(-1) at a current density of 1 A g(-1), and good stability, even after 1000 charge/discharge cycles. The approach developed in this work provides a new view of making full use of sustainable resources endowed by nature, opening the avenue to designing and producing robust materials with great promising applications in high-performance energy-storage devices.

Effect of Surface Treatment on Performance of Electrode Material Based on Carbon Fiber Cloth

Directory of Open Access Journals (Sweden)

XU Jian

2018-01-01

Full Text Available The carbon fiber cloth was treated by surface treatment, and then it was used as the electrode substrate. The electrode material based on carbon fibers was synthesized by a galvanostatic electrodeposition method. The interface resistivity, electrochemical property and corrosion resistance of the CF/β-PbO2 electrode were characterized by four-probe method and electrochemical workstation, respectively. The results show that the surface roughness and chemical activity of the carbon fibers can be significantly improved through surface treatment. The carbon fibers possess the best chemical activity on the surface at the hot-air oxidation temperature of 400℃. Joint hot-air and liquid-phase oxidations show that the chemical activity of the carbon fibers on the surface is further improved, the grooves and pits on the surface of the carbon fibers are more obvious, after this treatment, the interface resistivity of the CF/β-PbO2 electrode reaches the minimum value of 6.19×10-5Ω·m, meanwhile, the conductivity and the electrochemical property of the CF/β-PbO2 electrode reaches the best, and with the best corrosion resistance, the corrosion rate is only 1.44×10-3g·cm-2·h-1.Thus, the interface resistivity, electrochemical property and corrosion resistance of the CF/β-PbO2 electrode depend on the the interface structure of the CF/β-PbO2 electrode obtained under different surface treatments.

Comparative study of graphene and its derivative materials as an electrode in OLEDs

Science.gov (United States)

Srivastava, Anshika; Kumar, Brijesh

2018-04-01

In current scenario, the organic materials have given a revolutionary evolution in the electronics industry. As, the organic light emitting diodes (OLEDs) have almost replaced the conventional technologies due to the use of organic based materials. However, the next generations OLEDs are intensively desired nowadays for high definition display technology. There are various concern involved in the successful design of OLEDs. Electrodes are one of the electrical conductors, which play a vital role in the construction of OLEDs. The performance of OLED is majorly affected by the material used for electrodes. Due to the requirement of transparent, flexible and inexpensive anodes in bottom emissive OLEDs, ITO was replaced by graphene material. Graphene is a single layer 2-dimensional transparent carbon allotrope which showed prodigious potential to escalate the device performance. Although graphene demonstrated impressive characteristics in various applications, it showed unfavorable work function for many other devices. Thus, derivative materials of graphene such as graphene oxide, graphane and β - graphdiyne were synthesized by several researchers. By comparing graphene and its derivatives as an anode of OLEDs, it has been found that graphene oxide showed the preeminent performance among all. In this paper, all the comparisons are investigated by using a standard device constructed by piling layers of anode/ m_MTDATA/ NPB/ Alq3: QAD/ Alq3/ cathode in TCAD ATLAS device simulator.

Coated carbon nanotube array electrodes

Science.gov (United States)

Ren, Zhifeng [Newton, MA; Wen, Jian [Newton, MA; Chen, Jinghua [Chestnut Hill, MA; Huang, Zhongping [Belmont, MA; Wang, Dezhi [Wellesley, MA

2008-10-28

The present invention provides conductive carbon nanotube (CNT) electrode materials comprising aligned CNT substrates coated with an electrically conducting polymer, and the fabrication of electrodes for use in high performance electrical energy storage devices. In particular, the present invention provides conductive CNTs electrode material whose electrical properties render them especially suitable for use in high efficiency rechargeable batteries. The present invention also provides methods for obtaining surface modified conductive CNT electrode materials comprising an array of individual linear, aligned CNTs having a uniform surface coating of an electrically conductive polymer such as polypyrrole, and their use in electrical energy storage devices.

Determination of equilibration kinetics of oxide electrode materials using a manometric method

International Nuclear Information System (INIS)

Badwal, S.P.S.; Jiang, S.P.; Love, J.; Nowotny, J.; Rekas, M.

1998-01-01

The gas/solid equilibration kinetics for electrode oxide materials, such as (La 0.8 Sr 0.2 )MnO 3 , using a manometric method, was determined. The reaction kinetics between oxygen and the oxide material was monitored using the measurements of the P(O 2 ) changes during isothermic experiments of oxidation and reduction. The procedure of the determination will be described and relevant kinetic equations was derived. The equilibration kinetic data obtained can be used to determine the chemical diffusion coefficient. Copyright (1998) Australasian Ceramic Society

Beyond Slurry-Cast Supercapacitor Electrodes: PAN/MWNT Heteromat-Mediated Ultrahigh Capacitance Electrode Sheets

Science.gov (United States)

Lee, Jung Han; Kim, Jeong A.; Kim, Ju-Myung; Lee, Sun-Young; Yeon, Sun-Hwa; Lee, Sang-Young

2017-01-01

Supercapacitors (SCs) have garnered considerable attention as an appealing power source for forthcoming smart energy era. An ultimate challenge facing the SCs is the acquisition of higher energy density without impairing their other electrochemical properties. Herein, we demonstrate a new class of polyacrylonitrile (PAN)/multi-walled carbon tube (MWNT) heteromat-mediated ultrahigh capacitance electrode sheets as an unusual electrode architecture strategy to address the aforementioned issue. Vanadium pentoxide (V2O5) is chosen as a model electrode material to explore the feasibility of the suggested concept. The heteromat V2O5 electrode sheets are produced through one-pot fabrication based on concurrent electrospraying (for V2O5 precursor/MWNT) and electrospinning (for PAN nanofiber) followed by calcination, leading to compact packing of V2O5 materials in intimate contact with MWNTs and PAN nanofibers. As a consequence, the heteromat V2O5 electrode sheets offer three-dimensionally bicontinuous electron (arising from MWNT networks)/ion (from spatially reticulated interstitial voids to be filled with liquid electrolytes) conduction pathways, thereby facilitating redox reaction kinetics of V2O5 materials. In addition, elimination of heavy metallic foil current collectors, in combination with the dense packing of V2O5 materials, significantly increases (electrode sheet-based) specific capacitances far beyond those accessible with conventional slurry-cast electrodes.

Polyaniline silver nanoparticle coffee waste extracted porous graphene oxide nanocomposite structures as novel electrode material for rechargeable batteries

Science.gov (United States)

Sundriyal, Poonam; Bhattacharya, Shantanu

2017-03-01

The exploration of new and advanced electrode materials are required in electronic and electrical devices for power storage applications. Also, there has been a continuous endeavour to formulate strategies for extraction of high performance electrode materials from naturally obtained waste products. In this work, we have developed an in situ hybrid nanocomposite from coffee waste extracted porous graphene oxide (CEPG), polyaniline (PANI) and silver nanoparticles (Ag) and have found this novel composite to serve as an efficient electrode material for batteries. The successful interaction among the three phases of the nano-composite i.e. CEPG-PANI-Ag have been thoroughly understood through RAMAN, Fourier transform infrared and x-ray diffraction spectroscopy, morphological studies through field emission scanning electron microscope and transmission electron microscope. Thermo-gravimetric analysis of the nano-composite demonstrates higher thermal stability up-to a temperature of 495 °C. Further BET studies through nitrogen adsorption-desorption isotherms confirm the presence of micro/meso and macro-pores in the nanocomposite sample. The cyclic-voltammetry (CV) analysis performed on CEPG-PANI-Ag nanocomposite exhibits a purely faradic behaviour using nickel foam as a current collector thus suggests the prepared nanocomposite as a battery electrode material. The nanocomposite reports a maximum specific capacity of 1428 C g-1 and excellent cyclic stability up-to 5000 cycles.

Mn2C sheet as an electrode material for lithium-ion battery: A first-principles prediction

International Nuclear Information System (INIS)

Zhou, Yungang; Zu, Xiaotao

2017-01-01

Graphical abstract: Combined with strong Li bond, low Li diffusion barrier, superior electrical conductivity and high theoretical capacity, Mn 2 C Sheet is found to be a new promising electrode material for Lithium-Ion Battery. - Highlights: • Li atom bind strongly with Mn 2 C sheet with a very low adsorption energy. • Pristine Mn 2 C sheet exhibits metallic character. • Li atom can easily and freely migrate on the Mn 2 C sheet. • Lithiation to a high content is feasible. • Theoretical capacity of Mn 2 C sheet arrives at 879 mAhg −1 . - Abstract: A search for high-efficiency electrode materials is crucial for the application of Li-ion batteries (LIBs). Using density functional theory (DFT), we assess the Mn 2 C sheet, a new MXene, as a suitable electrode material. Our studies show that Li atoms can bind strongly to the Mn 2 C sheet, with low adsorption energy of −1.93 eV. A pristine Mn 2 C sheet exhibits metallic characteristic, offering an intrinsic advantage for the transportation of electrons in material. A very low energy barrier of 0.05 eV is predicted, showing that Li ion can easily and freely migrate on the Mn 2 C sheet. In addition, with the increase of Li content, adsorption energy varies minimally within a range of energy that spans only 0.27 eV, showing that lithiation to a high content is feasible. Furthermore, we found that, because of the bilayer adsorptions on both sides of the Mn 2 C sheet, the theoretical capacity of the Mn 2 C sheet is 879 mAhg −1 , which is greater than that of most two-dimentional (2D) electrode materials. All these results reveal a new promising MXene material for LIBs. We also studied the effects of oxidation and fluorination on the electrochemical properties of the Mn 2 C sheet and found that oxidation and fluorination will fade the electrochemical properties of the Mn 2 C sheet in general.

Compressed multiwall carbon nanotube composite electrodes provide enhanced electroanalytical performance for determination of serotonin

International Nuclear Information System (INIS)

Fagan-Murphy, Aidan; Patel, Bhavik Anil

2014-01-01

Serotonin (5-HT) is an important neurochemical that is present in high concentrations within the intestinal tract. Carbon fibre and boron-doped diamond based electrodes have been widely used to date for monitoring 5-HT, however these electrodes are prone to fouling and are difficult to fabricate in certain sizes and geometries. Carbon nanotubes have shown potential as a suitable material for electroanalytical monitoring of 5-HT but can be difficult to manipulate into a suitable form. The fabrication of composite electrodes is an approach that can shape conductive materials into practical electrode geometries suitable for biological environments. This work investigated how compression of multiwall carbon nanotubes (MWCNTs) epoxy composite electrodes can influence their electroanalytical performance. Highly compressed composite electrodes displayed significant improvements in their electrochemical properties along with decreased internal and charge transfer resistance, reproducible behaviour and improved batch to batch variability when compared to non-compressed composite electrodes. Compression of MWCNT epoxy composite electrodes resulted in an increased current response for potassium ferricyanide, ruthenium hexaammine and dopamine, by preferentially removing the epoxy during compression and increasing the electrochemical active surface of the final electrode. For the detection of serotonin, compressed electrodes have a lower limit of detection and improved sensitivity compared to non-compressed electrodes. Fouling studies were carried out in 10 μM serotonin where the MWCNT compressed electrodes were shown to be less prone to fouling than non-compressed electrodes. This work indicates that the compression of MWCNT carbon-epoxy can result in a highly conductive material that can be moulded to various geometries, thus providing scope for electroanalytical measurements and the production of a wide range of analytical devices for a variety of systems

Investigation of Ir-modified carbon felt as the positive electrode of an all-vanadium redox flow battery

International Nuclear Information System (INIS)

Wang, W.H.; Wang, X.D.

2007-01-01

Porous graphite felts have been used as electrode materials for all-vanadium redox flow batteries due to their wide operating potential range, stability as both an anode and a cathode, and availability in high surface area. In this paper, the carbon felt was modified by pyrolysis of Ir reduced from H 2 IrCl 6 . ac impedance and steady-state polarization measurements showed that the Ir-modified materials have improved activity and lowered overpotential of the desired V(IV)/V(V) redox process. Ir-modification of carbon felt enhanced the electro-conductivity of electrode materials. The Ir-material, when coated on the graphite felt electrode surface, lowered the cell internal resistance. A test cell was assembled with the Ir-modified carbon felt as the activation layer of the positive electrode, the unmodified raw felt as the activation layer of the negative electrode. At an operating current density of 20 mA cm -2 , a voltage efficiency of 87.5% was achieved. The resistance of the cell using Ir-modified felt decreased 25% compared to the cell using non-modified felt

Investigation on Electrochemical Properties of Polythiophene Nanocomposite with Graphite Derivatives as Supercapacitor Material on Breath Figure-Decorated PMMA Electrode

Science.gov (United States)

Azimi, Mona; Abbaspour, Mohsen; Fazli, Ali; Setoodeh, Hamideh; Pourabbas, Behzad

2018-03-01

Breath figures have been formed by the direct breath figure method on polymethyl methacrylate electrode sand hexagonal oriented holes with 0.5- to 10- μm2 surface area have been created. Deposition of materials on the electrodes has been performed by the spray-coating method. polythiophene (PTh) nanoparticles, polythiophene-graphene oxide (PTh-GO) and polythiophene-reduced graphene oxide (PTh-G) nanocomposites were synthesized by emulsion polymerization, while characterization of synthetic materials have been carried out by Fourier transform infrared, Χ-ray diffraction, transmission electron microscopy, UV-Vis spectroscopy and field emission scanning electron microscopy techniques. Also, the electrochemical properties of the designed electrodes were investigated by cyclic voltammetry, galvanostatic charge-discharge and electrochemical impedance spectroscopy techniques. Specific capacitance of porous electrodes coated by PTh nanoparticles, PTh-GO and PTh-G nanocomposites were calculated from cyclic voltammetry curves at 5 mV/s scan rate, andthe values are 3.5 F/g, 16.39 F/g, and 28.68 F/g, respectively. Also, the energy density of each electrode at 5 mV/s scan rate has been calculated and the results show that incorporation of GO and G nanolayers with PTh nanoparticles enhances the electrochemical properties of electrodes.

Synthesis and characterization of prospective polyanionic electrode materials for high performance energy storage applications

Science.gov (United States)

Jayachandran, M.; Durai, G.; Vijayakumar, T.

2018-04-01

In the present study, Polyanionic compound (SO4)-group based on Li2Ni(SO4)2 (Lithium Nickel Sulphate) composite electrodes materials were prepared by a ball-milling method and solid-state reaction route. X-ray diffraction analysis confirmed the formation of a polycrystalline orthorhombic phase of composite Li2Ni(SO4)2 with an average crystallite size of about 50.16 nm. Field Emission Scanning electron microscopy investigation reveals the spherical shape particles with the particle size of around 200–500 nm. Raman and FTIR analysis confirms the structural and functional groups of the synthesized materials and also the formation of Li2Ni(SO4)2. The electrochemical measurements using cyclic voltammetry (CV) and galvanostatic charging-discharging (GCD) techniques were carried out to study the electrochemical supercapacitive performance of the composite Li2Ni (SO4)2 electrodes. From the CV investigations, an areal capacitance of 508 mF cm‑2 was obtained at 10 mV s‑1. The galvanostatic charge-discharge (GCD) measurements exhibited the areal capacitance of 101 mF cm‑2 at a constant current density of 2 mA cm‑2 in 2 M KOH. These GCD profiles were linear and also symmetric in nature with the maximum columbic efficiency of about 85%. The electrochemical performance of the composite Li2Ni(SO4)2 electrode material shows excellent performance for supercapacitor applications.

IrOx-carbon nanotube hybrids: a nanostructured material for electrodes with increased charge capacity in neural systems.

Science.gov (United States)

Carretero, Nina M; Lichtenstein, Mathieu P; Pérez, Estela; Cabana, Laura; Suñol, Cristina; Casañ-Pastor, Nieves

2014-10-01

Nanostructured iridium oxide-carbon nanotube hybrids (IrOx-CNT) deposited as thin films by dynamic electrochemical methods are suggested as novel materials for neural electrodes. Single-walled carbon nanotubes (SWCNT) serve as scaffolds for growing the oxide, yielding a tridimensional structure with improved physical, chemical and electrical properties, in addition to high biocompatibility. In biological environments, SWCNT encapsulation by IrOx makes more resistant electrodes and prevents the nanotube release to the media, preventing cellular toxicity. Chemical, electrochemical, structural and surface characterization of the hybrids has been accomplished. The high performance of the material in electrochemical measurements and the significant increase in cathodal charge storage capacity obtained for the hybrid in comparison with bare IrOx represent a significant advance in electric field application in biosystems, while its cyclability is also an order of magnitude greater than pure IrOx. Moreover, experiments using in vitro neuronal cultures suggest high biocompatibility for IrOx-CNT coatings and full functionality of neurons, validating this material for use in neural electrodes. Copyright © 2014 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.

Development of Novel Electrode Materials for the Electrocatalysis of Oxygen-Transfer and Hydrogen-Transfer Reactions

Energy Technology Data Exchange (ETDEWEB)

Simpson, Brett Kimball [Iowa State Univ., Ames, IA (United States)

2002-01-01

Throughout this thesis, the fundamental aspects involved in the electrocatalysis of anodic O-transfer reactions and cathodic H-transfer reactions have been studied. The investigation into anodic O-transfer reactions at undoped and Fe(III)[doped MnO₂ films] revealed that MnO₂ film electrodes prepared by a cycling voltammetry deposition show improved response for DMSO oxidation at the film electrodes vs. the Au substrate. Doping of the MnO₂ films with Fe(III) further enhanced electrode activity. Reasons for this increase are believed to involve the adsorption of DMSO by the Fe(III) sites. The investigation into anodic O-transfer reactions at undoped and Fe(III)-doped RuO₂ films showed that the Fe(III)-doped RuO₂-film electrodes are applicable for anodic detection of sulfur compounds. The Fe(III) sites in the Fe-RuO₂ films are speculated to act as adsorption sites for the sulfur species while the Ru(IV) sites function for anodic discharge of H₂O to generate the adsorbed OH species. The investigation into cathodic H-transfer reactions, specifically nitrate reduction, at various pure metals and their alloys demonstrated that the incorporation of metals into alloy materials can create a material that exhibits bifunctional properties for the various steps involved in the overall nitrate reduction reaction. The Sb₁₀Sn₂₀Ti₇₀, Cu₆₃Ni₃₇ and Cu₂₅Ni₇₅ alloy electrodes exhibited improved activity for nitrate reduction as compared to their pure component metals. The Cu₆₃Ni₃₇ alloy displayed the highest activity for nitrate reduction. The final investigation was a detailed study of the electrocatalytic activity of cathodic H-transfer reactions (nitrate reduction) at various compositions of Cu-Ni alloy electrodes. Voltammetric response for NO₃^- at the Cu-Ni alloy electrode is superior to

MXene–2D layered electrode materials for energy storage

Directory of Open Access Journals (Sweden)

Hao Tang

2018-04-01

Full Text Available As promising candidates of power resources, electrochemical energy storage (EES devices have drawn more and more attention due to their ease of use, environmental friendliness, and high transformation efficiency. The performances of EES devices, such as lithium-ion batteries, sodium-ion batteries, and supercapacitors, depend largely on the inherent properties of electrode materials. On account of the outstanding properties of graphene, a lot of studies have been carried out on two-dimensional (2D materials. Over the past few years, a new exfoliation method has been utilized to successfully prepare a new family of 2D transition metal carbides, nitrides, and carbonitrides, termed MXene, from layered precursors. Moreover, some unique EES properties of MXene have been discovered. With rapid research progress on this field, a timely account about the applications of MXene in the EES fields is highly necessary. In this article, the research progress on the preparation, electrochemical performance, and mechanism analysis of MXene is summarized and discussed. We also propose some personal prospects for the further development of this field. Keywords: MXene, 2D materials, Electrochemistry, Battery, Supercapacitor

Graphite electrode DC arc furnace system for treatment of environmentally undesirable solid waste

International Nuclear Information System (INIS)

Titus, C.H.

1993-01-01

A gas tight DC arc furnace system using graphite electrodes is ideally suited for destruction of organic materials, compaction of metallic materials, and vitrification of inorganic waste materials. A graphite electrode DC arc furnace system which was developed by Electro-Pyrolysis, Inc. has been used to demonstrate that iron basalt soil containing various surrogate nonradioactive materials found on Department of Energy's Atomic Energy Sites and hospital waste can be reduced to a compact, vitrified, solid material which is environmentally acceptable and will pass TCLP leachate tests. A second graphite electrode DC arc furnace system is presently under construction and will be in operation at MIT during the second quarter of 1993. This furnace system is designed for demonstration of waste treatment and stabilization at a rate of 500 pounds per hour and will also be used for development and performance evaluation of diagnostic techniques and equipment for measuring and understanding internal furnace temperature profiles, gas entrained particulate composition, and particulate size distribution in various locations in the furnace during operation

Development of Hydrogen Electrodes for Alkaline Water Electrolysis

DEFF Research Database (Denmark)

Kjartansdóttir, Cecilía Kristín

, production of electricity via fuel cells, fuel for internal combustion engines or gas turbines, or as a raw material for the production of synthetic fuels via Sabatier or Fischer - Tropsch process. In some situations it may be suitable to simply inject hydrogen into the existing natural gas based...... will be needed. Producing hydrogen via water electrolysis using surplus, low cost, power from renewables offers the possibility of increased production capacity and load management with no greenhouse emissions. Hydrogen is a valuable energy carrier, which is able to contribute to various forms of energy, such as...... infrastructure. Alkaline water electrolysis (AWE) is the current standard (stat of the art) for industrial large-scale water electrolysis systems. One of the main criteria for industrial AWE is efficient and durable electrodes. The aim of the present PhD study was to develop electrode materials for hydrogen...

MgO-templated carbon as a negative electrode material for Na-ion capacitors

Science.gov (United States)

Kado, Yuya; Soneda, Yasushi

2016-12-01

In this study, MgO-templated carbon with different pore structures was investigated as a negative electrode material for Na-ion capacitors. With increasing the Brunauer-Emmett-Teller surface area, the irreversible capacity increased, and the coulombic efficiency of the 1st cycle decreased because of the formation of solid electrolyte interface layers. MgO-templated carbon annealed at 1000 °C exhibited the highest capacity and best rate performance, suggesting that an appropriate balance between surface area and crystallinity is imperative for fast Na-ion storage, attributed to the storage mechanism: combination of non-faradaic electric double-layer capacitance and faradaic Na intercalation in the carbon layers. Finally, a Na-ion capacitor cell using MgO-templated carbon and activated carbon as the negative and positive electrodes, respectively, exhibited an energy density at high power density significantly greater than that exhibited by the cell using a commercial hard carbon negative electrode.

Intercalated Water and Organic Molecules for Electrode Materials of Rechargeable Batteries.

Science.gov (United States)

Lee, Hyeon Jeong; Shin, Jaeho; Choi, Jang Wook

2018-03-24

The intrinsic limitations of lithium-ion batteries (LIBs) with regard to safety, cost, and the availability of raw materials have promoted research on so-called "post-LIBs". The recent intense research of post-LIBs provides an invaluable lesson that existing electrode materials used in LIBs may not perform as well in post-LIBs, calling for new material designs compliant with emerging batteries based on new chemistries. One promising approach in this direction is the development of materials with intercalated water or organic molecules, as these materials demonstrate superior electrochemical performance in emerging battery systems. The enlarged ionic channel dimensions and effective shielding of the electrostatic interaction between carrier ions and the lattice host are the origins of the observed electrochemical performance. Moreover, these intercalants serve as interlayer pillars to sustain the framework for prolonged cycles. Representative examples of such intercalated materials applied to batteries based on Li + , Na + , Mg 2+ , and Zn 2+ ions and supercapacitors are considered, along with their impact in materials research. © 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Investigation of positive electrode materials based on MnO2 for lithium batteries

International Nuclear Information System (INIS)

Le, My Loan Phung; Lam, Thi Xuan Binh; Pham, Quoc Trung; Nguyen, Thi Phuong Thoa

2011-01-01

Various composite materials of MnO 2 /C have been synthesized by electrochemical deposition and then used for the synthesis of lithium manganese oxide (LiMn 2 O 4 ) spinel as a cathode material for lithium ion batteries. The structure and electrochemical properties of electrode materials based on MnO 2 /C, spinel LiMn 2 O 4 and doped spinel LiNi 0.5 Mn 1.5 O 4 have been studied. The influence of synthesis conditions on the structural and electrochemical properties of synthesized materials was investigated by x-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electronic microscopy (TEM) and charge–discharge experiments. Some of the studied materials exhibit good performance of cycling and discharge capacity

Arcing time analysis of liquid nitrogen with respect to electrode materials

Science.gov (United States)

Junaid, Muhammad; Yang, Kun; Ge, Hanming; Wang, Jianhua

2018-03-01

Unlike sulphur hexafluoride (SF6), liquid nitrogen (LN2) is cost effective, environment friendly and cryogenic dielectric. It has astounding insulating properties with the potential to decrease power loss in switchgear applications due to its remarkably low temperatures. The basic research is however a necessity to observe the performance of LN2 subjected to high luminance arcs. So far, there are no findings that refer to the arcing time inside the LN2 environment. The objective of this work was to investigate the arcing times in LN2 and compare the results with open air conditions using different electrode materials. Experiments were conducted on different DC voltages and their arcing times were measured. Three different kinds of electrode materials, namely: pure copper (Cu), stainless used steel (SUS) and aluminium alloy (Al 6061) were tested under 1 atmospheric pressure. The results revealed that LN2 extinguishes arc in almost half the amount of time required by the open air insulation. With Al 6061 has the shortest arcing time, whilst Cu, the second best choice and SUS places last in the evaluation. It was encapsulated from the findings that LN2 is a better choice than air insulation in terms of arc quenching and a better alternative to SF6 when environment is the priority.

Hemi-ordered nanoporous carbon electrode material for highly selective determination of nitrite in physiological and environmental systems

Energy Technology Data Exchange (ETDEWEB)

Zhou, Shenghai; Wu, Hongmin; Wu, Ying; Shi, Hongyan; Feng, Xun; Jiang, Shang; Chen, Jian; Song, Wenbo, E-mail: wbsong@jlu.edu.cn

2014-08-01

Hemi-ordered nanoporous carbon (HONC) was obtained from a mesoporous silica template through a nano-replication method using furfuryl alcohol as the carbon source. The structure and morphology of HONC were characterized and analyzed in detail by X-ray diffraction, N{sub 2}-sorption, Raman spectroscopy and transmission electron microscopy. HONC was then demonstrated as active electrode material for selective determination of nitrite in either physiological or environmental system. Well separated oxidation peaks of ascorbic acid, dopamine, uric acid and nitrite were observed in physiological system, and simultaneous discrimination of catechol, hydroquinone, resorcinol and nitrite in environmental system was also accomplished. Distinctly improved performances for selective determination of nitrite (such as significantly fast and sensitive current response with especially high selectivity) coexisted with ascorbic acid, dopamine and uric acid in the physiological system, as well as with catechol, hydroquinone and resorcinol in the environmental system were achieved at HONC electrode material. The excellent discriminating ability and high selectivity for NO{sub 2}{sup −} determination were ascribed to the good electronic conductivity, unique hemi-ordered porous structure, large surface area and large number of edge plane defect sites contained on the surface of nanopore walls of HONC. Results in this work demonstrated that HONC is one of the promising catalytic electrode materials for nitrite sensor fabrication. - Highlights: • Hemi-ordered nanoporous carbon as an active electrode material • Good discriminating ability towards NO{sub 2}{sup −} from physiological or environmental system • Highly selective determination of nitrite with fast and sensitive current response.

Layer by Layer Ex-Situ Deposited Cobalt-Manganese Oxide as Composite Electrode Material for Electrochemical Capacitor.

Science.gov (United States)

Rusi; Chan, P Y; Majid, S R

2015-01-01

The composite metal oxide electrode films were fabricated using ex situ electrodeposition method with further heating treatment at 300°C. The obtained composite metal oxide film had a spherical structure with mass loading from 0.13 to 0.21 mg cm(-2). The structure and elements of the composite was investigated using X-ray diffraction (XRD) and energy dispersive X-ray (EDX). The electrochemical performance of different composite metal oxides was studied by cyclic voltammetry (CV) and galvanostatic charge-discharge (CD). As an active electrode material for a supercapacitor, the Co-Mn composite electrode exhibits a specific capacitance of 285 Fg(-1) at current density of 1.85 Ag(-1) in 0.5 M Na2SO4 electrolyte. The best composite electrode, Co-Mn electrode was then further studied in various electrolytes (i.e., 0.5 M KOH and 0.5 M KOH/0.04 M K3Fe(CN) 6 electrolytes). The pseudocapacitive nature of the material of Co-Mn lead to a high specific capacitance of 2.2 x 10(3) Fg(-1) and an energy density of 309 Whkg(-1) in a 0.5 M KOH/0.04 M K3Fe(CN) 6 electrolyte at a current density of 10 Ag(-1). The specific capacitance retention obtained 67% of its initial value after 750 cycles. The results indicate that the ex situ deposited composite metal oxide nanoparticles have promising potential in future practical applications.

International control of nuclear materials

International Nuclear Information System (INIS)

Koponen, Hannu

1989-01-01

Nuclear materials are subject to both national and international safeguards control. The International Atomic Energy Agency (IAEA) takes care of the international safeguards control. The control activities, which are discussed in this article, are carried out according to the agreements between various countries and the IAEA

Near-Electrode Imager

Energy Technology Data Exchange (ETDEWEB)

Rathke, Jerome W.; Klingler, Robert J.; Woelk, Klaus; Gerald, Rex E.,II

1999-05-01

An apparatus, near-electrode imager, for employing nuclear magnetic resonance imaging to provide in situ measurements of electrochemical properties of a sample as a function of distance from a working electrode. The near-electrode imager use the radio frequency field gradient within a cylindrical toroid cavity resonator to provide high-resolution nuclear magnetic resonance spectral information on electrolyte materials.

Contribution of tin in electrochemical properties of zinc antimonate nanostructures: An electrode material for supercapacitors

Science.gov (United States)

Balasubramaniam, M.; Balakumar, S.

2018-04-01

Tin (Sn) doped ZnSb2O6 nanostructures was synthesized by chemical precipitation method and was used as an electrode material for supercapacitors to explore its electrochemical stability and potentiality as energy storage materials. Their characteristic structural, morphological and compositional features were investigated through XRD, FESEM and XPS analysis. Results showed that the nanostructures have well ordered crystalline features with spherical particle morphology. As the size and morphology are the vital parameters in exhibiting better electrochemical properties, the prepared nanostructures exhibited a significant specific capacitance of 222 F/g at a current density of 0.5 A/g respectively. While charging and discharging for 1000 cycles, the capacitance retention was enhanced to 105.0% which depicts the stability and activeness of electrochemical sites present in the Sn doped ZnSb2O6 nanostructures even after cycling. Hence, the inclusion of Sn into ZnSb2O6 has contributed in improving the electrochemical properties thereby it represents itself as a potential electrode material for supercapacitors.

Band Gap Engineering of Boron Nitride by Graphene and Its Application as Positive Electrode Material in Asymmetric Supercapacitor Device.

Science.gov (United States)

Saha, Sanjit; Jana, Milan; Khanra, Partha; Samanta, Pranab; Koo, Hyeyoung; Murmu, Naresh Chandra; Kuila, Tapas

2015-07-08

Nanostructured hexagonal boron nitride (h-BN)/reduced graphene oxide (RGO) composite is prepared by insertion of h-BN into the graphene oxide through hydrothermal reaction. Formation of the super lattice is confirmed by the existence of two separate UV-visible absorption edges corresponding to two different band gaps. The composite materials show enhanced electrical conductivity as compared to the bulk h-BN. A high specific capacitance of ∼824 F g(-1) is achieved at a current density of 4 A g(-1) for the composite in three-electrode electrochemical measurement. The potential window of the composite electrode lies in the range from -0.1 to 0.5 V in 6 M aqueous KOH electrolyte. The operating voltage is increased to 1.4 V in asymmetric supercapacitor (ASC) device where the thermally reduced graphene oxide is used as the negative electrode and the h-BN/RGO composite as the positive electrode. The ASC exhibits a specific capacitance of 145.7 F g(-1) at a current density of 6 A g(-1) and high energy density of 39.6 W h kg(-1) corresponding to a large power density of ∼4200 W kg(-1). Therefore, a facile hydrothermal route is demonstrated for the first time to utilize h-BN-based composite materials as energy storage electrode materials for supercapacitor applications.

Anionic Redox Chemistry in Polysulfide Electrode Materials for Rechargeable Batteries.

Science.gov (United States)

Grayfer, Ekaterina D; Pazhetnov, Egor M; Kozlova, Mariia N; Artemkina, Sofya B; Fedorov, Vladimir E

2017-12-22

Classical Li-ion battery technology is based on the insertion of lithium ions into cathode materials involving metal (cationic) redox reactions. However, this vision is now being reconsidered, as many new-generation electrode materials with enhanced reversible capacities operate through combined cationic and anionic (non-metal) reversible redox processes or even exclusively through anionic redox transformations. Anionic participation in the redox reactions is observed in materials with more pronounced covalency, which is less typical for oxides, but quite common for phosphides or chalcogenides. In this Concept, we would like to draw the reader's attention to this new idea, especially, as it applies to transition-metal polychalcogenides, such as FeS 2 , VS 4 , TiS 3 , NbS 3 , TiS 4 , MoS 3 , etc., in which the key role is played by the (S-S) 2- /2 S 2- redox reaction. The exploration and better understanding of the anion-driven chemistry is important for designing advanced materials for battery and other energy-related applications. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Nanostructured MnO2 as Electrode Materials for Energy Storage

Science.gov (United States)

Mauger, Alain

2017-01-01

Manganese dioxides, inorganic materials which have been used in industry for more than a century, now find great renewal of interest for storage and conversion of energy applications. In this review article, we report the properties of MnO2 nanomaterials with different morphologies. Techniques used for the synthesis, structural, physical properties, and electrochemical performances of periodic and aperiodic frameworks are discussed. The effect of the morphology of nanosized MnO2 particles on their fundamental features is evidenced. Applications as electrodes in lithium batteries and supercapacitors are examined. PMID:29149066

Nanostructured MnO2 as Electrode Materials for Energy Storage

Directory of Open Access Journals (Sweden)

Christian M. Julien

2017-11-01

Full Text Available Manganese dioxides, inorganic materials which have been used in industry for more than a century, now find great renewal of interest for storage and conversion of energy applications. In this review article, we report the properties of MnO2 nanomaterials with different morphologies. Techniques used for the synthesis, structural, physical properties, and electrochemical performances of periodic and aperiodic frameworks are discussed. The effect of the morphology of nanosized MnO2 particles on their fundamental features is evidenced. Applications as electrodes in lithium batteries and supercapacitors are examined.

Novel Synthesis of 3D Graphene-CNF Electrode Architectures for Supercapacitor Applications

Science.gov (United States)

2013-06-01

executed the program detailed in Table 3. The software suite collected the diffracted data and compared the results to the database of the International ...collector with the active material facing upward. Following the electrode insertion, a Celgard 3501 2 µm microporous monolayer membrane (surfactant...K. S. Subrahmanyam and A. Govindaraj, “Graphene: The New Two-Dimensional Nanomaterial,” Angewandte Chemie- International Edition, vol. 48, pp. 7752

Aging Mechanisms of Electrode Materials in Lithium-Ion Batteries for Electric Vehicles

Directory of Open Access Journals (Sweden)

Cheng Lin

2015-01-01

Full Text Available Electrode material aging leads to a decrease in capacity and/or a rise in resistance of the whole cell and thus can dramatically affect the performance of lithium-ion batteries. Furthermore, the aging phenomena are extremely complicated to describe due to the coupling of various factors. In this review, we give an interpretation of capacity/power fading of electrode-oriented aging mechanisms under cycling and various storage conditions for metallic oxide-based cathodes and carbon-based anodes. For the cathode of lithium-ion batteries, the mechanical stress and strain resulting from the lithium ions insertion and extraction predominantly lead to structural disordering. Another important aging mechanism is the metal dissolution from the cathode and the subsequent deposition on the anode. For the anode, the main aging mechanisms are the loss of recyclable lithium ions caused by the formation and increasing growth of a solid electrolyte interphase (SEI and the mechanical fatigue caused by the diffusion-induced stress on the carbon anode particles. Additionally, electrode aging largely depends on the electrochemical behaviour under cycling and storage conditions and results from both structural/morphological changes and side reactions aggravated by decomposition products and protic impurities in the electrolyte.

Dielectric elastomers with novel highly-conducting electrodes

Science.gov (United States)

Böse, Holger; Uhl, Detlev

2013-04-01

Beside the characteristics of the elastomer material itself, the performance of dielectric elastomers in actuator, sensor as well as generator applications depends also on the properties of the electrode material. Various electrode materials based on metallic particles dispersed in a silicone matrix were manufactured and investigated. Anisotropic particles such as silver-coated copper flakes and silver-coated glass flakes were used for the preparation of the electrodes. The concentration of the metallic particles and the thickness of the electrode layers were varied. Specific conductivities derived from resistance measurements reached about 100 S/cm and surmount those of the reference materials based on graphite and carbon black by up to three orders of magnitude. The high conductivities of the new electrode materials can be maintained even at very large stretch deformations up to 200 %.

Negative electrodes for Na-ion batteries.

Science.gov (United States)

Dahbi, Mouad; Yabuuchi, Naoaki; Kubota, Kei; Tokiwa, Kazuyasu; Komaba, Shinichi

2014-08-07

Research interest in Na-ion batteries has increased rapidly because of the environmental friendliness of sodium compared to lithium. Throughout this Perspective paper, we report and review recent scientific advances in the field of negative electrode materials used for Na-ion batteries. This paper sheds light on negative electrode materials for Na-ion batteries: carbonaceous materials, oxides/phosphates (as sodium insertion materials), sodium alloy/compounds and so on. These electrode materials have different reaction mechanisms for electrochemical sodiation/desodiation processes. Moreover, not only sodiation-active materials but also binders, current collectors, electrolytes and electrode/electrolyte interphase and its stabilization are essential for long cycle life Na-ion batteries. This paper also addresses the prospect of Na-ion batteries as low-cost and long-life batteries with relatively high-energy density as their potential competitive edge over the commercialized Li-ion batteries.

NdFeB alloy as a magnetic electrode material for lithium-ion batteries

International Nuclear Information System (INIS)

Zhang, J.; Shui, J.L.; Zhang, S.L.; Wei, X.; Xiang, Y.J.; Xie, S.; Zhu, C.F.; Chen, C.H.

2005-01-01

The search for a reliable indicator of state of charge and even the remaining energy of a lithium-ion cell is of great importance for various applications. This study was an exploratory effort to use magnetic susceptibility as the indicator. In this work, for the first time the change of ac susceptibility of cells was in situ monitored during charge-discharge process. A strong permanent magnetic material, NdFeB alloy, was investigated as an anode material for rechargeable lithium batteries. Both original and partially oxidized NdFeB powders were made into electrodes. Structural characterization was performed on the NdFeB electrodes by means of X-ray diffraction (XRD) and scanning electron microscopy (SEM) analysis. An alloy (core)-oxide (shell) structure was found for those partially oxidized samples. The electrochemical cycling of cells made of the NdFeB electrodes against lithium was measured. The first lithium intercalation capacity of a treated NdFeB can be up to about 831 mAh/g, while a rather reversible capacity of up to 352 mAh/g can be obtained. With a specially designed cell, we were able to monitor in situ the change of relative ac susceptibility during charge and/or discharge steps. A clearly monotonous relationship is found between the ac susceptibility of a cell and its depth-of-discharge (DOD). A mechanism based on skin effect and eddy current change is proposed to explain this susceptibility versus DOD relationship

NdFeB alloy as a magnetic electrode material for lithium-ion batteries

Energy Technology Data Exchange (ETDEWEB)

Zhang, J. [Department of Materials Science and Engineering, University of Science and Technology of China, Anhui Hefei 230026 (China); Shui, J.L. [Department of Materials Science and Engineering, University of Science and Technology of China, Anhui Hefei 230026 (China); Zhang, S.L. [Department of Materials Science and Engineering, University of Science and Technology of China, Anhui Hefei 230026 (China); Wei, X. [Department of Materials Science and Engineering, University of Science and Technology of China, Anhui Hefei 230026 (China); Xiang, Y.J. [Department of Materials Science and Engineering, University of Science and Technology of China, Anhui Hefei 230026 (China); Xie, S. [Department of Materials Science and Engineering, University of Science and Technology of China, Anhui Hefei 230026 (China); Zhu, C.F. [Department of Materials Science and Engineering, University of Science and Technology of China, Anhui Hefei 230026 (China); Chen, C.H. [Department of Materials Science and Engineering, University of Science and Technology of China, Anhui Hefei 230026 (China)]. E-mail: cchchen@ustc.edu.cn

2005-04-05

The search for a reliable indicator of state of charge and even the remaining energy of a lithium-ion cell is of great importance for various applications. This study was an exploratory effort to use magnetic susceptibility as the indicator. In this work, for the first time the change of ac susceptibility of cells was in situ monitored during charge-discharge process. A strong permanent magnetic material, NdFeB alloy, was investigated as an anode material for rechargeable lithium batteries. Both original and partially oxidized NdFeB powders were made into electrodes. Structural characterization was performed on the NdFeB electrodes by means of X-ray diffraction (XRD) and scanning electron microscopy (SEM) analysis. An alloy (core)-oxide (shell) structure was found for those partially oxidized samples. The electrochemical cycling of cells made of the NdFeB electrodes against lithium was measured. The first lithium intercalation capacity of a treated NdFeB can be up to about 831 mAh/g, while a rather reversible capacity of up to 352 mAh/g can be obtained. With a specially designed cell, we were able to monitor in situ the change of relative ac susceptibility during charge and/or discharge steps. A clearly monotonous relationship is found between the ac susceptibility of a cell and its depth-of-discharge (DOD). A mechanism based on skin effect and eddy current change is proposed to explain this susceptibility versus DOD relationship.

Rapid synthesis of monodispersed highly porous spinel nickel cobaltite (NiCo{sub 2}O{sub 4}) electrode material for supercapacitors

Energy Technology Data Exchange (ETDEWEB)

Naveen, A. Nirmalesh, E-mail: nirmalesh.naveen@gmail.com; Selladurai, S. [Ionics Laboratory, Department of Physics, Anna University, Chennai-600025 (India)

2015-06-24

Monodispersed highly porous spinel nickel cobaltite electrode material was successfully synthesized in a short time using combustion technique. Single phase cubic nature of the spinel nickel cobaltite with average crystallite size of 24 nm was determined from X-ray diffraction study. Functional groups present in the compound were determined from FTIR study and it further confirms the spinel formation. FESEM images reveal the porous nature of the prepared material and uniform size distribution of the particles. Electrochemical evaluation was performed using Cyclic Voltammetry (CV) technique, Chronopotentiometry (CP) and Electrochemical Impedance Spectroscopy (EIS). Results reveal the typical pseudocapacitive behaviour of the material. Maximum capacitance of 754 F/g was calculated at the scan rate of 5 mV/s, high capacitance was due to the unique porous morphology of the electrode. Nyquist plot depicts the low resistance and good electrical conductivity of nickel cobaltite. It has been found that nickel cobaltite prepared by this typical method will be a potential electrode material for supercapcitor application.

Extended abstracts of the 8. international symposium on new materials and nano-materials for electrochemical systems : emerging trends and challenges in new materials development for sustainable energy and environment

International Nuclear Information System (INIS)

Savadogo, O.; Ma, Z.F.

2010-01-01

This conference provided a forum to highlight the advances made in the development of new materials and nano-materials for electrochemical systems, including fuel cells. Electrochemical energy system devices have the potential to provide new applications for high power mobile systems as an alternative to internal combustion engines. They also have the potential for applications in hand-held personal electronic devices, uninterrupted power supply and auxiliary power supply. However, additional advances in unit cell material and design are still needed before mass production of fuel cells can begin. Cost, reliability, service life, electrode performance and power density are among the technical challenges facing commercialization. In addition to a plenary and general session, the sessions of the conference were entitled: low temperature fuel cells; high temperature fuel cells; advanced secondary rechargeable batteries; hydrogen production and storage; electrochemical supercapacitors; and poster session. All 166 presentations at this conference have been catalogued separately for inclusion in this database

Reliability of electrode wear compensation based on material removal per discharge in micro EDM milling

DEFF Research Database (Denmark)

Bissacco, Giuliano; Tristo, G.; Hansen, Hans Nørgaard

2013-01-01

This paper investigates the reliability of workpiece material removal per discharge (MRD) estimation for application in electrode wear compensation based on workpiece material removal. An experimental investigation involving discharge counting and automatic on the machine measurement of removed...... material volume was carried out in a range of process parameters settings from fine finishing to roughing. MRD showed a decreasing trend with the progress of the machining operation, reaching stabilization after a number of machined layers. Using the information on MRD and discharge counting, a material...

Facile Synthesis of MnPO4·H2O Nanowire/Graphene Oxide Composite Material and Its Application as Electrode Material for High Performance Supercapacitors

Directory of Open Access Journals (Sweden)

Bo Yan

2016-12-01

Full Text Available In this work, we reported a facile one-pot hydrothermal method to synthesize MnPO4·H2O nanowire/graphene oxide composite material with coated graphene oxide. Transmission electron microscopy and scanning electron microscope were employed to study its morphology information, and X-ray diffraction was used to study the phase and structure of the material. Additionally, X-ray photoelectron spectroscopy was used to study the elements information. To measure electrochemical performances of electrode materials and the symmetry cell, cyclic voltammetry, chronopotentiometry and electrochemical impedance spectrometry were conducted on electrochemical workstation using 3 M KOH electrolytes. Importantly, electrochemical results showed that the as-prepared MnPO4·H2O nanowire/graphene oxide composite material exhibited high specific capacitance (287.9 F·g−1 at 0.625 A·g−1 and specific power (1.5 × 105 W·kg−1 at 2.271 Wh·kg−1, which is expected to have promising applications as supercapacitor electrode material.

Development and characterisation of a novel composite electrode material consisting of poly(3,4-ethylenedioxythiophene) including Au nanoparticles

International Nuclear Information System (INIS)

Zanardi, C.; Terzi, F.; Pigani, L.; Heras, A.; Colina, A.; Lopez-Palacios, J.; Seeber, R.

2008-01-01

Composite material consisting of poly(3,4-ethylenedioxythiophene) (PEDOT), including Au nanoparticles encapsulated by N-dodecyl-N,N-dimethyl-3-ammonium-1-propanesulphonate (SB12) is synthesised by constant-current method on ITO glass, in aqueous medium, leading to an electrode coating. The synthesis process is followed by UV-vis spectroelectrochemistry, both in normal-beam and in parallel-beam configurations. Under the same experimental conditions PEDOT is also synthesised by electropolymerisation only in the presence of LiClO 4 supporting electrolyte, as well in solutions also containing SB12. The data relative to the electrosynthesis of the three materials are compared. The composite material based on the conductive polymer matrix including Au nanoparticles has been characterised by SEM, TEM, ICP, Raman and UV-vis spectroscopies. The behaviour of the three different electrode coatings with respect to p-doping process has been studied by conventional electrochemical techniques and by potentiostatic and potentiodynamic UV-vis spectroelectrochemical methods. Conclusions are drawn out about the effect of the presence of the surfactant and of Au nanoparticles on the electrochemical properties of the electrode system

Nickel cobalt oxide nanowire-reduced graphite oxide composite material and its application for high performance supercapacitor electrode material.

Science.gov (United States)

Wang, Xu; Yan, Chaoyi; Sumboja, Afriyanti; Lee, Pooi See

2014-09-01

In this paper, we report a facile synthesis method of mesoporous nickel cobalt oxide (NiCo2O4) nanowire-reduced graphite oxide (rGO) composite material by urea induced hydrolysis reaction, followed by sintering at 300 degrees C. P123 was used to stabilize the GO during synthesis, which resulted in a uniform coating of NiCo2O4 nanowire on rGO sheet. The growth mechanism of the composite material is discussed in detail. The NiCo2O4-rGO composite material showed an outstanding electrochemical performance of 873 F g(-1) at 0.5 A g(-1) and 512 F g(-1) at 40 A g(-1). This method provides a promising approach towards low cost and large scale production of supercapacitor electrode material.

Hierarchical Co3O4/PANI hollow nanocages: Synthesis and application for electrode materials of supercapacitors

Science.gov (United States)

Ren, Xiaohu; Fan, Huiqing; Ma, Jiangwei; Wang, Chao; Zhang, Mingchang; Zhao, Nan

2018-05-01

Hierarchically hollow Co3O4/polyaniline nanocages (Co3O4/PANI NCs) with enhanced specific capacitance and cycle performance for electrode material of supercapacitors are fabricated by combining self-sacrificing template and in situ polymerization route. Benefiting from the good conductivity of PANI improving an electron transport rate as well as high specific surface area from such a hollow structure, the electrode made of Co3O4/PANI NCs exhibits a large specific capacitance of 1301 F/g at the current density of 1 A/g, a much enhancement is obtained as compared with the pristine Co3O4 NCs electrode. The contact resistance (Re), charge-transfer (Rct) and Warburg resistance of Co3O4/PANI NCs electrode is significantly lower than that of the pristine Co3O4 NCs electrode, indicating the enhanced electrical conductivity. In addition, the Co3O4/PANI NCs electrode also displays superior cycling stability with 90 % capacitance retention after 2000 cycles. Moreover, an aqueous asymmetric supercapacitor was successfully assembled using Co3O4/PANI NCs as the positive electrode and activated carbon (AC) as the negative electrode, the assembled device exhibits a superior energy density of 41.5 Wh/kg at 0.8 kW/kg, outstanding power density of 15.9 kW/kg at 18.4 Wh/kg, which significantly transcending those of most previously reported. These results demonstrate that the hierarchically hollow Co3O4/PANI NCs composites have a potential for fabricating electrode of supercapacitors.

Graphene-based materials for supercapacitor electrodes – A review

Directory of Open Access Journals (Sweden)

Qingqing Ke

2016-03-01

Full Text Available The graphene-based materials are promising for applications in supercapacitors and other energy storage devices due to the intriguing properties, i.e., highly tunable surface area, outstanding electrical conductivity, good chemical stability and excellent mechanical behavior. This review summarizes recent development on graphene-based materials for supercapacitor electrodes, based on their macrostructural complexity, i.e., zero-dimensional (0D (e.g. free-standing graphene dots and particles, one-dimensional (1D (e.g. fiber-type and yarn-type structures, two-dimensional (2D (e.g. graphenes and graphene-based nanocomposite films, and three-dimensional (3D (e.g. graphene foam and hydrogel-based nanocomposites. There are extensive and on-going researches on the rationalization of their structures at varying scales and dimensions, development of effective and low cost synthesis techniques, design and architecturing of graphene-based materials, as well as clarification of their electrochemical performance. It is indicated that future studies should focus on the overall device performance in energy storage devices and large-scale process in low costs for the promising applications in portable and wearable electronic, transport, electrical and hybrid vehicles.

Stable switching of resistive random access memory on the nanotip array electrodes

KAUST Repository

Tsai, Kun-Tong

2016-09-13

The formation/rupture of conducting filaments (CFs) in resistive random access memory (ReRAM) materials tune the electrical conductivities non-volatilely and are largely affected by its material composition [1], internal configurations [2] and external environments [3,4]. Therefore, controlling repetitive formation/rupture of CF as well as the spatial uniformity of formed CF are fundamentally important for improving the resistive switching (RS) performance. In this context, we have shown that by adding a field initiator, typically a textured electrode, both performance and switching uniformity of ReRAMs can be improved dramatically [5]. In addition, despite its promising characteristics, the scalable fabrication and structural homogeneity of such nanostructured electrodes are still lacking or unattainable, making miniaturization of ReRAM devices an exceeding challenge. Here, we employ nanostructured electrode (nanotip arrays, extremely uniform) formed spontaneously via a self-organized process to improve the ZnO ReRAM switching characteristics.

Hierarchical Heterostructures of NiCo2O4@XMoO4 (X = Ni, Co) as an Electrode Material for High-Performance Supercapacitors.

Science.gov (United States)

Hu, Jiyu; Qian, Feng; Song, Guosheng; Wang, Linlin

2016-12-01

Hierarchical heterostructures of NiCo2O4@XMoO4 (X = Ni, Co) were developed as an electrode material for supercapacitor with improved pseudocapacitive performance. Within these hierarchical heterostructures, the mesoporous NiCo2O4 nanosheet arrays directly grown on the Ni foam can not only act as an excellent pseudocapacitive material but also serve as a hierarchical scaffold for growing NiMoO4 or CoMoO4 electroactive materials (nanosheets). The electrode made of NiCo2O4@NiMoO4 presented a highest areal capacitance of 3.74 F/cm(2) at 2 mA/cm(2), which was much higher than the electrodes made of NiCo2O4@CoMoO4 (2.452 F/cm(2)) and NiCo2O4 (0.456 F/cm(2)), respectively. Meanwhile, the NiCo2O4@NiMoO4 electrode exhibited good rate capability. It suggested the potential of the hierarchical heterostructures of NiCo2O4@CoMoO4 as an electrode material in supercapacitors.

Positive electrode for lithium secondary battery of the next generation. Part 3. Positive electrode active material synthesized by soft chemistry; 3 sofutokemisutori de gosei sareru seikyoku katsubusshitsu

Energy Technology Data Exchange (ETDEWEB)

Kumagai, N.; Jo, A [Iwate Univ., Morioka (Japan). Faculty of Engineering

1997-10-05

Synthesis of high performance positive electrode material for the lithium secondary battery using soft chemistry methods such as sol-gel method, precipitation method, and ion exchange method as well as the electrochemical properties and the positive electrode material for the metal oxides synthesized by soft chemistry methods are introduced. V2O5 gel is obtained by acidifying aqueous solution of vanadate such as NaVO3. MnO2 exists in various crystalline forms, and the characteristics of the electrode depend strongly on the crystal structure, chemical composition, water content, conditions of powder, and density, which can be controlled by the methods of synthesis and heat treatment. Sol-gel method is applied to the synthesis of MnO2 related compounds. LiCoO2 is synthesized by the precipitation method of the aqueous solution of the mixture of lithium hydroxide and ammonium hydroxide. Tungsten trioxide hydrate and molybdenum trioxide hydrate are obtained as precipitation by adding strong acid for acidification to tungstate or molybdate A2MO4 aqueous solution. 31 refs., 8 figs.

Computational modelling of internally cooled wet (ICW) electrodes for radiofrequency ablation: impact of rehydration, thermal convection and electrical conductivity.

Science.gov (United States)

Trujillo, Macarena; Bon, Jose; Berjano, Enrique

2017-09-01

(1) To analyse rehydration, thermal convection and increased electrical conductivity as the three phenomena which distinguish the performance of internally cooled electrodes (IC) and internally cooled wet (ICW) electrodes during radiofrequency ablation (RFA), (2) Implement a RFA computer model with an ICW which includes these phenomena and (3) Assess their relative influence on the thermal and electrical tissue response and on the coagulation zone size. A 12-min RFA in liver was modelled using an ICW electrode (17 G, 3 cm tip) by an impedance-control pulsing protocol with a constant current of 1.5 A. A model of an IC electrode was used to compare the ICW electrode performance and the computational results with the experimental results. Rehydration and increased electrical conductivity were responsible for an increase in coagulation zone size and a delay (or absence) in the occurrence of abrupt increases in electrical impedance (roll-off). While the increased electrical conductivity had a remarkable effect on enlarging the coagulation zone (an increase of 0.74 cm for differences in electrical conductivity of 0.31 S/m), rehydration considerably affected the delay in roll-off, which, in fact, was absent with a sufficiently high rehydration level. In contrast, thermal convection had an insignificant effect for the flow rates considered (0.05 and 1 mL/min). Computer results suggest that rehydration and increased electrical conductivity were mainly responsible for the absence of roll-off and increased size of the coagulation zone, respectively, and in combination allow the thermal and electrical performance of ICW electrodes to be modelled during RFA.

Improved Manufacturing Performance of Screen Printed Carbon Electrodes through Material Formulation.

Science.gov (United States)

Jewell, Eifion; Philip, Bruce; Greenwood, Peter

2016-06-27

Printed carbon graphite materials are the primary common component in the majority of screen printed sensors. Screen printing allows a scalable manufacturing solution, accelerating the means by which novel sensing materials can make the transition from laboratory material to commercial product. A common bottleneck in any thick film printing process is the controlled drying of the carbon paste material. A study has been undertaken which examines the interaction between material solvent, printed film conductivity and process consistency. The study illustrates that it is possible to reduce the solvent boiling point to significantly increase process productivity while maintaining process consistency. The lower boiling point solvent also has a beneficial effect on the conductivity of the film, reducing the sheet resistance. It is proposed that this is a result of greater film stressing increasing charge percolation through greater inter particle contact. Simulations of material performance and drying illustrate that a multi layered printing provides a more time efficient manufacturing method. The findings have implications for the volume manufacturing of the carbon sensor electrodes but also have implications for other applications where conductive carbon is used, such as electrical circuits and photovoltaic devices.

Hydrothermal synthesis of Mn-doped ZnCo2O4 electrode material for high-performance supercapacitor

Science.gov (United States)

Mary, A. Juliet Christina; Bose, A. Chandra

2017-12-01

Mn-doped ZnCo2O4 nanoparticle has been synthesized by hydrothermal method without adding any surfactants. Structural, morphological and electrochemical performances have been studied for the pure and various concentration of Mn-doped ZnCo2O4 nanoparticles. XRD and Raman studies demonstrate the crystalline structure of the material. Specific capacitance of the 10 wt% Mn doped ZnCo2O4 nanomaterial is analysed using the three-electrode system. 10 wt% Mn-doped ZnCo2O4 has a maximum capacitance of 707.4 F g-1 at a current density of 0.5 A g-1. Coulombic efficiency of the material is 96.3% for 500 cycles in the KOH electrolyte medium. A two-electrode device using 10 wt% Mn-doped ZnCo2O4 exhibits the highest specific capacitance of 6.5 F g-1 at a current density of 0.03 A g-1 which is the suitable material for supercapacitor application.

Facile synthesis of birnessite-type manganese oxide nanoparticles as supercapacitor electrode materials.

Science.gov (United States)

Liu, Lihu; Luo, Yao; Tan, Wenfeng; Zhang, Yashan; Liu, Fan; Qiu, Guohong

2016-11-15

Manganese oxides are environmentally benign supercapacitor electrode materials and, in particular, birnessite-type structure shows very promising electrochemical performance. In this work, nanostructured birnessite was facilely prepared by adding dropwise NH2OH·HCl to KMnO4 solution under ambient temperature and pressure. In order to fully exploit the potential of birnessite-type manganese oxide electrode materials, the effects of specific surface area, pore size, content of K(+), and manganese average oxidation state (Mn AOS) on their electrochemical performance were studied. The results showed that with the increase of NH2OH·HCl, the Mn AOS decreased and the corresponding pore sizes and specific surface area of birnessite increased. The synthesized nanostructured birnessite showed the highest specific capacitance of 245Fg(-1) at a current density of 0.1Ag(-1) within a potential range of 0-0.9V, and excellent cycle stability with a capacitance retention rate of 92% after 3000 cycles at a current density of 1.0Ag(-1). The present work implies that specific capacitance is mainly affected by specific surface area and pore volume, and provides a new method for the facile preparation of birnessite-type manganese oxide with excellent capacitive performance. Copyright © 2016 Elsevier Inc. All rights reserved.

Electrochemical investigation of thermically treated graphene oxides as electrode materials for vanadium redox flow battery

International Nuclear Information System (INIS)

Di Blasi, O.; Briguglio, N.; Busacca, C.; Ferraro, M.; Antonucci, V.; Di Blasi, A.

2015-01-01

Highlights: • Graphene oxide is synthesized at high temperatures in a reducing environment. • Treated graphene oxide-based electrodes are prepared by the wet impregnation method. • Electrochemical performance is evaluated as a function of the physico-chemical properties. - Abstract: Thermically treated graphene oxides (TT-GOs) are synthesized at different temperatures, 100 °C, 150 °C, 200 °C and 300 °C in a reducing environment (20% H 2 /He) and investigated as electrode materials for vanadium redox flow battery (VRFB) applications. The treated graphene oxide-based electrodes are prepared by the wet impregnation method using carbon felt (CF) as support. The main aim is to achieve a suitable distribution of the dispersed graphene oxides on the CF surface in order to investigate the electrocatalytic activity for the VO 2+ /VO 2 + and V 2+ /V 3+ redox reactions in the perspective of a feasible large area electrodes scale-up for battery configuration of practical interest. Cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) are carried out in a three electrode half-cell to characterize the electrochemical properties of the TT-GO-based electrodes. Physico-chemical characterizations are carried out to corroborate the electrochemical results. The TT-GO sample treated at 100 °C (TT-GO-100) shows the highest electrocatalytic activity in terms of peak to peak separation (ΔE = 0.03 V) and current density intensity (∼0.24 A cm −2 at 30 mV/s) both toward the VO 2+ /VO 2 + and V 2+ /V 3+ redox reactions. This result is correlated to the presence of hydroxyl (−OH) and carboxyl (−COOH) species that act as active sites. A valid candidate is individuated as effective anode and cathode electrode in the perspective of electrodes scale-up for battery configuration of practical interest

Catalyst Stability Benchmarking for the Oxygen Evolution Reaction: The Importance of Backing Electrode Material and Dissolution in Accelerated Aging Studies.

Science.gov (United States)

Geiger, Simon; Kasian, Olga; Mingers, Andrea M; Nicley, Shannon S; Haenen, Ken; Mayrhofer, Karl J J; Cherevko, Serhiy

2017-09-18

In searching for alternative oxygen evolution reaction (OER) catalysts for acidic water splitting, fast screening of the material intrinsic activity and stability in half-cell tests is of vital importance. The screening process significantly accelerates the discovery of new promising materials without the need of time-consuming real-cell analysis. In commonly employed tests, a conclusion on the catalyst stability is drawn solely on the basis of electrochemical data, for example, by evaluating potential-versus-time profiles. Herein important limitations of such approaches, which are related to the degradation of the backing electrode material, are demonstrated. State-of-the-art Ir-black powder is investigated for OER activity and for dissolution as a function of the backing electrode material. Even at very short time intervals materials like glassy carbon passivate, increasing the contact resistance and concealing the degradation phenomena of the electrocatalyst itself. Alternative backing electrodes like gold and boron-doped diamond show better stability and are thus recommended for short accelerated aging investigations. Moreover, parallel quantification of dissolution products in the electrolyte is shown to be of great importance for comparing OER catalyst feasibility. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Film of lignocellulosic carbon material for self-supporting electrodes in electric double-layer capacitors

Directory of Open Access Journals (Sweden)

Tsubasa Funabashi

2013-09-01

Full Text Available A novel thin, wood-based carbon material with heterogeneous pores, film of lignocellulosic carbon material (FLCM, was successfully fabricated by carbonizing softwood samples of Picea jezoensis (Jezo spruce. Simultaneous increase in the specific surface area of FLCM and its affinity for electrolyte solvents in an electric double-layer capacitor (EDLC were achieved by the vacuum ultraviolet/ozone (VUV/O3 treatment. This treatment increased the specific surface area of FLCM by 50% over that of original FLCM. The results obtained in this study confirmed that FLCM is an appropriate self-supporting EDLC electrode material without any warps and cracks.

Transparent Electrodes for Efficient Optoelectronics

KAUST Repository

Morales-Masis, Monica

2017-03-30

With the development of new generations of optoelectronic devices that combine high performance and novel functionalities (e.g., flexibility/bendability, adaptability, semi or full transparency), several classes of transparent electrodes have been developed in recent years. These range from optimized transparent conductive oxides (TCOs), which are historically the most commonly used transparent electrodes, to new electrodes made from nano- and 2D materials (e.g., metal nanowire networks and graphene), and to hybrid electrodes that integrate TCOs or dielectrics with nanowires, metal grids, or ultrathin metal films. Here, the most relevant transparent electrodes developed to date are introduced, their fundamental properties are described, and their materials are classified according to specific application requirements in high efficiency solar cells and flexible organic light-emitting diodes (OLEDs). This information serves as a guideline for selecting and developing appropriate transparent electrodes according to intended application requirements and functionality.

Transparent Electrodes for Efficient Optoelectronics

KAUST Repository

Morales-Masis, Monica; De Wolf, Stefaan; Woods-Robinson, Rachel; Ager, Joel W.; Ballif, Christophe

2017-01-01

With the development of new generations of optoelectronic devices that combine high performance and novel functionalities (e.g., flexibility/bendability, adaptability, semi or full transparency), several classes of transparent electrodes have been developed in recent years. These range from optimized transparent conductive oxides (TCOs), which are historically the most commonly used transparent electrodes, to new electrodes made from nano- and 2D materials (e.g., metal nanowire networks and graphene), and to hybrid electrodes that integrate TCOs or dielectrics with nanowires, metal grids, or ultrathin metal films. Here, the most relevant transparent electrodes developed to date are introduced, their fundamental properties are described, and their materials are classified according to specific application requirements in high efficiency solar cells and flexible organic light-emitting diodes (OLEDs). This information serves as a guideline for selecting and developing appropriate transparent electrodes according to intended application requirements and functionality.

Advanced screening of electrode couples

Science.gov (United States)

Giner, J. D.; Cahill, K.

1980-01-01

The chromium (Cr(3+)/Cr(2+)) redox couple (electrolyte and electrode) was investigated to determine its suitability as negative electrode for the iron (Fe(3+)/Fe(2+))-chromium (Cr(3+)/Cr(2+)) redox flow battery. Literature search and laboratory investigation established that the solubility and stability of aqueous acidic solutions of chromium(3) chloride and chromium(2) chloride are sufficient for redox battery application. Four categories of electrode materials were tested; namely, metals and metalloid materials (elements and compounds), alloys, plated materials, and Teflon-bonded materials. In all, the relative performance of 26 candidate electrode materials was evaluated on the basis of slow scan rate linear sweep voltammetry in stirred solution. No single material tested gave both acceptable anodic an acceptable cathodic performance. However, the identification of lead as a good cathodic electrocatalyst and gold as a good anodic electrocatalyst led to the invention of the lead/gold combination electrocatalyst. This type of catalyst can be fabricated in several ways and appears to offer the advantages of each metal without the disadvantages associated with their use as single materials. This lead/gold electrocatalyst was tested by NASA-Lewis Research Center in complete, flowing, redox batteries comprising a stack of several cells. A large improvement in the battery's coulombic and energy efficiency was observed.

Improved electrochemical performance of polyindole/carbon nanotubes composite as electrode material for supercapacitors

Science.gov (United States)

Cai, Zhi-Jiang; Zhang, Qin; Song, Xian-You

2016-09-01

Polyindole/carbon nanotubes (PIN/CNTs) composite was prepared by an in-situ chemical oxidative polymerization of indole monomer with CNTs using ammonium persulfate as oxidant. The obtained composite material was characterized by SEM, TEM, FT-IR, Raman spectroscopy, XPS, XRD and BET surface areas measurements. It was found that the CNTs were incorporated into the PIN matrix and nanoporous structure was formed. Spectroscopy results showed that interfacial interaction bonds might be formed between the polyindole chains and CNTs during the in-situ polymerization. PIN/CNTs composite was evaluated by electrochemical impedance spectroscopy, cyclic voltammetry and charge/discharge tests to determine electrode performances in relation to supercapacitors properties in both aqueous and non-aqueous system. A maximum specific capacitance and specific volumetric capacitance of 555.6 F/g and 222.2 F/cm3 can be achieved at 0.5 A/g in non-aqueous system. It also displayed good rate performance and cycling stability. The specific capacitance retention is over 60% at 10 A/g and 91.3% after 5000 cycles at 2 A/g, respectively. These characteristics point to its promising applications in the electrode material for supercapacitors.

Electrode systems for in situ vitrification

Science.gov (United States)

Buelt, James L.; Carter, John G.; Eschbach, Eugene A.; FitzPatrick, Vincent F.; Koehmstedt, Paul L.; Morgan, William C.; Oma, Kenton H.; Timmerman, Craig L.

1990-01-01

An electrode comprising a molybdenum rod is received within a conductive collar formed of graphite. The molybdenum rod and the graphite collar may be physically joined at the bottom. A pair of such electrodes are placed in soil containing buried waste material and an electric current is passed therebetween for vitrifying the soil. The graphite collar enhances the thermal conductivity of the combination, bringing heat to the surface, and preventing formation of a cold cap of material above the ground surface. The annulus between the molybdenum rod electrode and the graphite collar is suitably filled with a conductive ceramic powder that sinters upon the molybdenum rod, protecting the same from oxidation as graphite material is consumed, or a metal powder which liquefies at operating temperatures. The center of the molybdenum rod, used with a collar of separately, can be hollow and filled with a powdered metal, such as copper, which liquefies at operating temperatures. Connection to electrodes can be provided below ground level to avoid open circuit due to electrode deterioration, or sacrificial electrodes may be employed when operation is started. Outboard electrodes cna be utilized to square up a vitrified area.

Graphene electrodes for stimulation of neuronal cells

International Nuclear Information System (INIS)

Koerbitzer, Berit; Nick, Christoph; Thielemann, Christiane; Krauss, Peter; Yadav, Sandeep; Schneider, Joerg J

2016-01-01

Graphene has the ability to improve the electrical interface between neuronal cells and electrodes used for recording and stimulation purposes. It provides a biocompatible coating for common electrode materials such as gold and improves the electrode properties. Graphene electrodes are also prepared on SiO 2 substrate to benefit from its optical properties like transparency. We perform electrochemical and Raman characterization of gold electrodes with graphene coating and compare them with graphene on SiO 2 substrate. It was found that the substrate plays an important role in the performance of graphene and show that graphene on SiO 2 substrate is a very promising material combination for stimulation electrodes. (paper)

Erosion on spark plug electrodes; Funkenerosion an Zuendkerzenelektroden

Energy Technology Data Exchange (ETDEWEB)

Rager, J.

2006-07-01

Durability of spark plugs is mainly determined by spark gap widening, caused by electrode wear. Knowledge about the erosion mechanisms of spark plug materials is of fundamental interest for the development of materials with a high resistance against electrode erosion. It is therefore crucial to identify those parameters which significantly influence the erosion behaviour of a material. In this work, a reliable and reproducible testing method is presented which produces and characterizes electrode wear under well-defined conditions and which is capable of altering parameters specifically. Endurance tests were carried out to study the dependence of the wear behaviour of pure nickel and platinum on the electrode temperature, gas, electrode gap, electrode diameter, atmospheric pressure, and partial pressure of oxygen. It was shown that erosion under nitrogen is negligible, irrespective of the material. This disproves all common mechanism discussed in the literature explaining material loss of spark plug electrodes. Based on this observation and the variation of the mentioned parameters a new erosion model was deduced. This relies on an oxidation of the electrode material and describes the erosion of nickel and platinum separately. For nickel, electrode wear is caused by the removal of an oxide layer by the spark. In the case of platinum, material loss occurs due to the plasma-assisted formation and subsequent evaporation of volatile oxides in the cathode spot. On the basis of this mechanism a new composite material was developed whose erosion resistance is superior to pure platinum. Oxidation resistant metal oxide particles were added to a platinum matrix, thus leading to a higher erosion resistance of the composite. However, this can be decreased by a side reaction, the separation of oxygen from the metal oxides, which effectively assists the oxidation of the matrix. This reaction can be suppressed by using highly stable oxides, characterized by a large negative Gibbs

New, Efficient, and Reliable Air Electrode Material for Proton-Conducting Reversible Solid Oxide Cells.

Science.gov (United States)

Huan, Daoming; Shi, Nai; Zhang, Lu; Tan, Wenzhou; Xie, Yun; Wang, Wanhua; Xia, Changrong; Peng, Ranran; Lu, Yalin

2018-01-17

Driven by the demand to minimize fluctuation in common renewable energies, reversible solid oxide cells (RSOCs) have drawn increasing attention for they can operate either as fuel cells to produce electricity or as electrolysis cells to store electricity. Unfortunately, development of proton-conducting RSOCs (P-RSOCs) faces a major challenge of poor reliability because of the high content of steam involved in air electrode reactions, which could seriously decay the lifetime of air electrode materials. In this work, a very stable and efficient air electrode, SrEu 2 Fe 1.8 Co 0.2 O 7-δ (SEFC) with layer structure, is designed and deployed in P-RSOCs. X-ray diffraction analysis and High-angle annular dark-filed scanning transmission electron microscopy images of SEFC reveal that Sr atoms occupy the center of perovskite slabs, whereas Eu atoms arrange orderly in the rock-salt layer. Such a special structure of SEFC largely depresses its Lewis basicity and therefore its reactivity with steam. Applying the SEFC air electrode, our button switches smoothly between both fuel cell and electrolysis cell (EC) modes with no obvious degradation over a 135 h long-term test under wet H 2 (∼3% H 2 O) and 10% H 2 O-air atmospheres. A record of over 230 h is achieved in the long-term stability test in the EC mode, doubling the longest test that had been previously reported. Besides good stability, SEFC demonstrates great catalytic activity toward air electrode reactions when compared with traditional La 0.6 Sr 0.4 Co 0.2 Fe 0.8 O 3-δ air electrodes. This research highlights the potential of stable and efficient P-RSOCs as an important part in a sustainable new energy power system.

Application of internal electrodes to the oesophageal and tracheal tube in an animal trial: evaluation of its clinical and technical potentiality in electrical impedance tomography.

Science.gov (United States)

Czaplik, Michael; Antink, Christoph Hoog; Rossaint, Rolf; Leonhardt, Steffen

2014-06-01

Electrical impedance tomography (EIT) is of potential medical interest e.g., to optimize ventilator settings during mechanical ventilation. Nevertheless there are still several challenges. Although electrode belts are commonly used and promoted, they are not necessarily adequate for the long-term monitoring of patients in intensive-care units (ICU). ICU patients are usually equipped with breathing tubes and feeding tubes, ideal surfaces to attach EIT electrodes to. The aim of our study was therefore to examine the potentiality of internal electrodes in a porcine animal trial. Following an animal trial protocol studying acute lung injury, additional EIT measurements were obtained both with conventional electrodes set upon a rubber belt and after having moved the electrodes internally in seven pigs. For this reason the two most dorsally located electrodes were selected. An adjacent stimulation and measurement pattern was used, and resulting voltages in the time and frequency domains as well as within reconstructed images were examined to compare perfusion and ventilation data qualitatively and quantitatively. Particularly, lung morphology as well as signal strength for both the mediastinal and lung region were studied. All animals were submitted to the additional protocol without any adverse events. Distinguishability of lungs was improved in reconstructed frames. The resulting sensitivity of measured electrical impedance was enhanced around the mediastinal region and even cardiac-related activity was significantly increased by a factor of up to 6. In conclusion the application of internal electrodes appears to be beneficial for diverse clinical purposes and should be addressed in further studies.

A porous carbon material from pyrolysis of fructus cannabis’s shells for supercapacitor electrode application

Science.gov (United States)

Li, Kai; Zhang, Wei-Bin; Zhao, Zhi-Yun; Zhao, Yue; Chen, Xi-Wen; Kong, Ling-Bin

2018-02-01

The porous carbon material is obtained via pyrolysis and activation of fructus cannabis’s shells, an easy-to-get biomass source, and is used as an active electrode material for supercapacitors. The obtained carbon exhibit a high specific surface area of 2389 m2 g-1. And the result of x-ray photoelectron spectroscopy (XPS) shows that the obtained porous carbon possess numerous oxygen groups, which can facilitate the wettability of the electrode. The prepared porous carbon also exhibit remarkable electrochemical properties, such as high specific capacitance of 357 F g-1 at a current density of 0.5 A g-1 in 6 mol L-1 aqueous KOH electrolyte, good rate capability of 77% capacitance retention as the current density increase from 0.5 A g-1 to 10 A g-1. In addition, it also presents a superior cycling stability of 100% capacitance retention after 10 000 cycles at the current density of 1 A g-1.

Preparation and property study of MnO2/CNPs as electrode materials of electrochemical supercapacitors

Directory of Open Access Journals (Sweden)

JIANG Chao

2016-12-01

Full Text Available MnO2 nanorods deposited on carbon nanospheres (MnO2/CNPs as electrode materials of electrochemical supercapacitors have been synthesized via a hydrothermal synthesis.The micro morphologies and phases of the as-prepared MnO2/CNPs were characterized by field emission scanning electro microscopy(FESEM and X-ray diffraction(XRD.The electrochemical properties of nanomaterials were tested by cyclic voltammetry and galvanostatic charge-discharge.At a current density of 0.1 A/g using 1 mol/L Na2SO4 as electrolyte,the as-prepared MnO2/CNPs exhibit excellent specific capacitance of 305.6 F/g,far larger than carbon nanospheres (49.3 F/g.At a current density of 5 A/g,the specific capacitance of MnO2/CNPs is 235 F/g,which is 76.9% of the specific capacitance under 1 A/g current density.These results demonstrated that MnO2/CNPs may show potential application for electrode materials in electrochemical supercapacitors.

International safeguards of fissionable material

International Nuclear Information System (INIS)

Tempus, P.

1991-01-01

From the very beginning nuclear fissile materials have been subject to state and - outside nuclear weapon states - also to international monitoring. The latter was a principal task of the International Atomic Energy Agency, a UN affiliated organisation formed in 1957 based in Vienna. The legal, technical and political aspects of its monitoring activity are explained

Atomic Layer Deposition on Porous Materials: Problems with Conventional Approaches to Catalyst and Fuel Cell Electrode Preparation

Directory of Open Access Journals (Sweden)

Tzia Ming Onn

2018-03-01

Full Text Available Atomic layer deposition (ALD offers exciting possibilities for controlling the structure and composition of surfaces on the atomic scale in heterogeneous catalysts and solid oxide fuel cell (SOFC electrodes. However, while ALD procedures and equipment are well developed for applications involving flat surfaces, the conditions required for ALD in porous materials with a large surface area need to be very different. The materials (e.g., rare earths and other functional oxides that are of interest for catalytic applications will also be different. For flat surfaces, rapid cycling, enabled by high carrier-gas flow rates, is necessary in order to rapidly grow thicker films. By contrast, ALD films in porous materials rarely need to be more than 1 nm thick. The elimination of diffusion gradients, efficient use of precursors, and ligand removal with less reactive precursors are the major factors that need to be controlled. In this review, criteria will be outlined for the successful use of ALD in porous materials. Examples of opportunities for using ALD to modify heterogeneous catalysts and SOFC electrodes will be given.

Accelerating rate calorimetry studies of the reactions between ionic liquids and charged lithium ion battery electrode materials

International Nuclear Information System (INIS)

Wang, Yadong; Zaghib, K.; Guerfi, A.; Bazito, Fernanda F.C.; Torresi, Roberto M.; Dahn, J.R.

2007-01-01

Using accelerating rate calorimetry (ARC), the reactivity between six ionic liquids (with and without added LiPF 6 ) and charged electrode materials is compared to the reactivity of standard carbonate-based solvents and electrolytes with the same electrode materials. The charged electrode materials used were Li 1 Si, Li 7 Ti 4 O 12 and Li 0.45 CoO 2 . The experiments showed that not all ionic liquids are safer than conventional electrolytes/solvents. Of the six ionic liquids tested, 1-ethyl-3-methylimidazolium bis(fluorosulfonyl)imide (EMI-FSI) shows the worst safety properties, and is much worse than conventional electrolyte. 1-Ethyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide (EMI-TFSI) and 1-propyl-1-methylpyrrolidinium bis(fluorosulfonyl)imide (Py13-FSI) show similar reactivity to carbonate-based electrolyte. The three ionic liquids 1-butyl-2,3-dimethylimidazolium bis(trifluoromethanesulfonyl)imide (BMMI-TFSI), 1-butyl-1-methylpiperidinium bis(trifluoromethanesulfonyl)imide (Pp14-TFSI) and N-trimethyl-N-butylammonium bis(trifluoromethanesulfonyl)imide (TMBA-TFSI) show similar reactivity and are much safer than the conventional carbonate-based electrolyte. A comparison of the reactivity of ionic liquids with common anions and cations shows that ionic liquids with TFSI - are safer than those with FSI - , and liquids with EMI + are worse than those with BMMI + , Py13 + , Pp14 + and TMBA +

Preparation and photoelectrocatalytic performance of N-doped TiO2/NaY zeolite membrane composite electrode material.

Science.gov (United States)

Cheng, Zhi-Lin; Han, Shuai

2016-01-01

A novel composite electrode material based on a N-doped TiO2-loaded NaY zeolite membrane (N-doped TiO2/NaY zeolite membrane) for photoelectrocatalysis was presented. X-ray diffraction (XRD), scanning electron microscopy (SEM), UV-visible (UV-vis) and X-ray photoelectron spectroscopy (XPS) characterization techniques were used to analyze the structure of the N-doped TiO2/NaY zeolite membrane. The XRD and SEM results verified that the N-doped TiO2 nanoparticles with the size of ca. 20 nm have been successfully loaded on the porous stainless steel-supported NaY zeolite membrane. The UV-vis result showed that the N-doped TiO2/NaY zeolite membrane exhibited a more obvious red-shift than that of N-TiO2 nanoparticles. The XPS characterization revealed that the doping of N element into TiO2 was successfully achieved. The photoelectrocatalysis performance of the N-doped TiO2/NaY zeolite membrane composite electrode material was evaluated by phenol removal and also the effects of reaction conditions on the catalytic performance were investigated. Owing to exhibiting an excellent catalytic activity and good recycling stability, the N-doped TiO2/NaY zeolite membrane composite electrode material was of promising application for photoelectrocatalysis in wastewater treatment.

Role of the Material Electrodes on Resistive Behaviour of Carbon Nanotube-Based Gas Sensors for H2S Detection

Directory of Open Access Journals (Sweden)

M. Lucci

2012-01-01

Full Text Available Miniaturized gas-sensing devices that use single-walled carbon nanotubes as active material have been fabricated using two different electrode materials, namely, Au/Cr and NbN. The resistive sensors have been assembled aligning by dielectrophoresis the nanotube bundles between 40 μm spaced Au/Cr or NbN multifinger electrodes. The sensing devices have been tested for detection of the H2S gas, in the concentration range 10–100 ppm, using N2 as carrier gas. No resistance changes were detected using sensor fabricated with NbN electrodes, whereas the response of the sensor fabricated with Au/Cr electrodes was characterized by an increase of the resistance upon gas exposure. The main performances of this sensor are a detection limit for H2S of 10 ppm and a recovery time of few minutes. The present study suggests that the mechanism involved in H2S gas detection is not a direct charge transfer between molecules and nanotubes. The hypothesis is that detection occurs through passivation of the Au surfaces by H2S molecules and modification of the contact resistance at the Au/nanotube interface.

Low-temperature self-assembled vertically aligned carbon nanofibers as counter-electrode material for dye-sensitized solar cells

International Nuclear Information System (INIS)

Mahpeykar, S M; Tabatabaei, M K; Ghafoori-fard, H; Habibiyan, H; Koohsorkhi, J

2013-01-01

Low-temperature AC–DC PECVD is employed for direct growth of vertically aligned carbon nanofibers (VACNFs) on ordinary transparent conductive glass as counter-electrode material for dye-sensitized solar cells (DSSCs). To the best of our knowledge, this is the first report on utilization of VACNFs grown directly on ordinary FTO-coated glass as a cost-effective catalyst material in DSSCs. According to the FESEM images, the as-grown arrays are well aligned and dense, and offer uniform coverage on the surface of the substrate. In-plane and out-of-plane conductivity measurements reveal their good electrical conductivity, and Raman spectroscopy suggests a high number of electrocatalytic active sites, favoring charge transport at the electrolyte/electrode interface. Hybrid VACNF/Pt electrodes are also fabricated for performance comparison with Pt and VACNF electrodes. X-ray diffraction results verify the crystallization of Pt in hybrid electrodes and further confirm the vertical alignment of carbon nanofibers. Electrochemical characterization indicates that VACNFs provide both high catalytic and good charge transfer capability, which can be attributed to their high surface area, defect-rich and one-dimensional structure, vertical alignment and low contact resistance. As a result, VACNF cells can achieve a comparable performance (∼5.6%) to that of the reference Pt cells (∼6.5%). Moreover, by combination of the excellent charge transport and catalytic ability of VACNFs and the high conductivity of Pt nanoparticles, hybrid VACNF/Pt cells can deliver a performance superior to that of the Pt cells (∼7.2%), despite having a much smaller amount of Pt loading, which raises hopes for low-cost large-scale production of DSSCs in the future. (paper)

One-dimensional nanostructured materials for lithium-ion battery and supercapacitor electrodes

Science.gov (United States)

Chan, Candace Kay

The need for improved electrochemical storage devices has necessitated research on new and advanced electrode materials. One-dimensional nanomaterials such as nanowires, nanotubes, and nanoribbons, can provide a unique opportunity to engineer electrochemical devices to have improved electronic and ionic conductivity as well as electrochemical and structural transformations. Silicon and germanium nanowires (NWs) were studied as negative electrode materials for lithiumion batteries because of their ability to alloy with large amounts of lithium, leading to 4-10 times higher specific capacities than the graphite standard. These nanowires could be grown vertically off of metallic current collector substrates using the gold-catalyzed vapor-liquid-solid synthesis. Electrochemical measurements of the SiNWs showed that capacities greater than 3,500 mAh/g could be obtained for tens of cycles, while hundreds of cycles could be obtained at lower capacities. As opposed to bulk Si, the SiNWs were observed to maintain their morphology during cycling and did not pulverize due to the large volume changes. Detailed TEM and XRD characterization showed that the SiNWs became amorphous during the first lithiation (charge) and formed a two-phase region between crystalline Si and amorphous Li xSi. Afterwards, the SiNWs remained amorphous and subsequent reaction was through a single-phase cycling of amorphous Si. The good cycling behavior compared to bulk and micron-sized Si particles was attributed to the nanowire morphology and electrode design. The surface chemistry and solid-electrolyte interphase (SEI) were studied using XPS as a function of charge and discharge potential. The common reduction productions expected in the electrolyte (1 M LiPF6 in 1:1 EC/DEC) were observed, with the main component being Li2CO3. The morphology of the SEI was found to change at different potentials, indicating a dynamic process involving deposition, dissolution, and re-deposition on the SiNWs. Longterm

Arc plasma assisted rotating electrode process for preparation of metal pebbles

International Nuclear Information System (INIS)

Mohanty, T.; Tripathi, B.M.; Mahata, T.; Sinha, P.K.

2014-01-01

Spherical beryllium pebbles of size ranging from 0.2-2 mm are required as neutron multiplying material in solid Test Blanket Module (TBM) of International Thermonuclear Experimental Reactor (ITER). Rotating electrode process (REP) has been identified as a suitable technique for preparation of beryllium pebbles. In REP, arc plasma generated between non-consumable electrode (cathode) and rotating metal electrode (anode) plays a major role for continuous consumption of metal electrode and preparation of spherical metal pebbles. This paper focuses on description of the process, selection of sub-systems for development of REP experimental set up and optimization of arc parameters, such as, cathode geometry, arc current, arc voltage, arc gap and carrier gas flow rate for preparation of required size spherical metal pebbles. Other parameters which affect the pebbles sizes are rotational speed, metal electrode diameter and physical properties of the metal. As beryllium is toxic in nature its surrogate metals such as stainless steel (SS) and Titanium (Ti) were selected to evaluate the performance of the REP equipment. Several experiments were carried out using SS and Ti electrode and process parameters have been optimized for preparation of pebbles of different sizes. (author)

Synthesis of a highly efficient 3D graphene-CNT-MnO2-PANI nanocomposite as a binder free electrode material for supercapacitors.

Science.gov (United States)

Asif, Muhammad; Tan, Yi; Pan, Lujun; Rashad, Muhammad; Li, Jiayan; Fu, Xin; Cui, Ruixue

2016-09-29

Graphene based nanocomposites have been investigated intensively, as electrode materials for energy storage applications. In the current work, a graphene-CNT-MnO 2 -PANI (GCM@PANI) nanocomposite has been synthesized on 3D graphene grown on nickel foam, as a highly efficient binder free electrode material for supercapacitors. Interestingly, the specific capacitance of the synthesized electrode increases up to the first 1500 charge-discharge cycles, and is thus referred to as an electrode activation process. The activated GCM@PANI nanocomposite electrode exhibits an extraordinary galvanostatic specific capacitance of 3037 F g -1 at a current density of 8 A g -1 . The synthesized nanocomposite exhibits an excellent cyclic stability with a capacitance retention of 83% over 12 000 charge-discharge cycles, and a high rate capability by retaining a specific capacitance of 84.6% at a current density of 20 A g -1 . The structural and electrochemical analysis of the synthesized nanocomposite suggests that the astonishing electrochemical performance might be attributed to the growth of a novel PANI nanoparticle layer and the synergistic effect of CNT/MnO 2 nanostructures.

The Influence of Materials of Electrodes of Sensitized Solar Cells on Their Capacitive and Electrical Characteristics

Science.gov (United States)

Lazarenko, P. I.; Kozyukhin, S. A.; Mokshina, A. I.; Sherchenkov, A. A.; Patrusheva, T. N.; Irgashev, R. A.; Lebedev, E. A.; Kozik, V. V.

2018-05-01

An estimation is made of the internal capacitance of sensitized solar cells (SSCs) manufactured by the method of extraction pyrolysis. The structures under study are characterized by a hysteresis in the current-voltage characteristic obtained in the direct and reverse modes of voltage variation. The investigations of SSCs demonstrate a high inertness of the parameters under connection and disconnection of the light source. The use of a transparent conductive ITO-electrode, manufactured by the extraction pyrolysis, increases the external capacitance of the cell and decelerates the processes of current decay after the light source connection compared to the commercial FTO-electrode. The values of charges, capacitances, and SSC charge conservation efficiencies are calculated and the internal resistance of the SSCs under study is estimated. According to the estimations performed, the specimen with an ITO-layer possesses a capacitance equal to C1 = 1.23·10-3 F, which is by two orders of magnitude higher than that of the specimen with a FTO-layer (C2 = 2.06·10-5 F).

Ion-selective electrode reviews

CERN Document Server

Thomas, J D R

1982-01-01

Ion-Selective Electrode Reviews, Volume 3, provides a review of articles on ion-selective electrodes (ISEs). The volume begins with an article on methods based on titration procedures for surfactant analysis, which have been developed for discrete batch operation and for continuous AutoAnalyser use. Separate chapters deal with detection limits of ion-selective electrodes; the possibility of using inorganic ion-exchange materials as ion-sensors; and the effect of solvent on potentials of cells with ion-selective electrodes. Also included is a chapter on advances in calibration procedures, the d

The effects of electrode materials on the conversion efficiency of a direct converter used in neutral beam injection systems

International Nuclear Information System (INIS)

Noda, Shunichi; Nagae, Hiroshi; Yano, Hidenobu; Masuda, Mitsuharu; Akazaki, Masanori

1986-01-01

The injection of fast neutral beams into plasmas is thought to be the most promising way for the fusion plasma heating. Fast neutral beams are obtained by injecting fast ions into a neutralizer cell, in which ions are neutralized through charge exchange collisions with the ambient gas. However, the neutralization efficiency in the neutralizer cell is so low that the net power may not be extracted from a fusion reactor unless the energy of the ions being not neutralized in the cell is recovered. The present paper describes some problems associated with the electrostatic direct energy recovery of fast ion beams for this purpose. The titanium and molybdenum were tested as the direct converter electrode materials, and it was found that the conversion efficiency and the conditioning process of the converter electrode depended strongly on the electrode material. The effect of secondary electrons emitted from the electron repeller on the conversion efficiency was also made clear in the present experiments. (author)

Accounting for Interference, Scattering, and Electrode Absorption to Make Accurate Internal Quantum Efficiency Measurements in Organic and Other Thin Solar Cells

KAUST Repository

Burkhard, George F.; Hoke, Eric T.; McGehee, Michael D.

2010-01-01

Accurately measuring internal quantum efficiency requires knowledge of absorption in the active layer of a solar cell. The experimentally accessible total absorption includes significant contributions from the electrodes and other nonactive layers. We suggest a straightforward method for calculating the active layer contribution that minimizes error by subtracting optically-modeled electrode absorption from experimentally measured total absorption. (Figure Presented) © 2010 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Accounting for Interference, Scattering, and Electrode Absorption to Make Accurate Internal Quantum Efficiency Measurements in Organic and Other Thin Solar Cells

KAUST Repository

Burkhard, George F.

2010-05-31

Accurately measuring internal quantum efficiency requires knowledge of absorption in the active layer of a solar cell. The experimentally accessible total absorption includes significant contributions from the electrodes and other nonactive layers. We suggest a straightforward method for calculating the active layer contribution that minimizes error by subtracting optically-modeled electrode absorption from experimentally measured total absorption. (Figure Presented) © 2010 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Characterization of Electrode Materials for Lithium Ion and Sodium Ion Batteries using Synchrotron Radiation Techniques

Energy Technology Data Exchange (ETDEWEB)

Mehta, Apurva; Stanford Synchrotron Radiation Lightsource; Doeff, Marca M.; Chen, Guoying; Cabana, Jordi; Richardson, Thomas J.; Mehta, Apurva; Shirpour, Mona; Duncan, Hugues; Kim, Chunjoong; Kam, Kinson C.; Conry, Thomas

2013-04-30

We describe the use of synchrotron X-ray absorption spectroscopy (XAS) and X-ray diffraction (XRD) techniques to probe details of intercalation/deintercalation processes in electrode materials for Li ion and Na ion batteries. Both in situ and ex situ experiments are used to understand structural behavior relevant to the operation of devices.

Perovskite electrodes and method of making the same

Science.gov (United States)

Seabaugh, Matthew M.; Swartz, Scott L.

2005-09-20

The invention relates to perovskite oxide electrode materials in which one or more of the elements Mg, Ni, Cu, and Zn are present as minority components that enhance electrochemical performance, as well as electrode products with these compositions and methods of making the electrode materials. Such electrodes are useful in electrochemical system applications such as solid oxide fuel cells, ceramic oxygen generation systems, gas sensors, ceramic membrane reactors, and ceramic electrochemical gas separation systems.

Cell with scrolled electrodes. Uzumaki jo denkyokutai wo sonaeta denchi

Energy Technology Data Exchange (ETDEWEB)

Kamibayashi, M.; Morioka, Y. (Sanyo Electric Co. Ltd., Osaka (Japan))

1990-10-03

Non-sintered electrode plates produced by direct filling of paste state active materials in metal fiber felt type porous body are proposed recently for use as electrode plates for alkali cells and the like. Although this type of electrode plates can be produced with a simple facility because sintering process is not required, it has a shorcoming of internal short circuiting because metal fibers pass through the separator due to fuzzing of metal fiber. According to this invention, a sheet comprising metallic fibers oriented at right angles against the scrolled direction of the electrode plate is stacked on the surface of the metal fiber felt type porous body sheet when it is scrolled with the interposed separator. As the result, fibers are not bent and does not protrude from the surface of sheet to pass through the separator because each metallic fiber comprising the metallic sheet on the surface are arranged at a right angle against the direction of scrolling of the porous sheet. 2 figs., 1 tab.

Design and synthesis of porous nano-sized Sn@C/graphene electrode material with 3D carbon network for high-performance lithium-ion batteries

Energy Technology Data Exchange (ETDEWEB)

Lian, Peichao, E-mail: lianpeichao@126.com [Faculty of Chemical Engineering, Kunming University of Science and Technology, Kunming 650500 (China); Wang, Jingyi [Faculty of Chemical Engineering, Kunming University of Science and Technology, Kunming 650500 (China); Cai, Dandan; Liu, Guoxue [School of Chemistry and Chemical Engineering, South China University of Technology, Guangzhou 510640 (China); Wang, Yingying [Faculty of Chemical Engineering, Kunming University of Science and Technology, Kunming 650500 (China); Wang, Haihui, E-mail: hhwang@scut.edu.cn [School of Chemistry and Chemical Engineering, South China University of Technology, Guangzhou 510640 (China)

2014-08-01

Highlights: • Porous nano-sized Sn@C/graphene electrode material was designed and prepared. • The preparation method presented here can avoid the agglomeration of nanoparticles. • The prepared Sn@C/graphene electrode material exhibits outstanding cyclability. - Abstract: Tin is a promising high-capacity anode material for lithium-ion batteries, but it usually suffers from the problem of poor cycling stability due to the large volume change during the charge–discharge process. In this article, porous nano-sized Sn@C/graphene electrode material with three-dimensional carbon network was designed and prepared. Reducing the size of the Sn particles to nanoscale can mitigate the absolute strain induced by the large volume change during lithiation–delithiation process, and retard particle pulverization. The porous structure can provide a void space, which helps to accommodate the volume changes of the Sn nanoparticles during the lithium uptake-release process. The carbon shell can avoid the aggregation of the Sn nanoparticles on the same piece of graphene and detachment of the pulverized Sn particles during the charge–discharge process. The 3D carbon network consisted of graphene sheets and carbon shells can not only play a structural buffering role in minimizing the mechanical stress caused by the volume change of Sn, but also keep the overall electrode highly conductive during the lithium uptake-release process. As a result, the as-prepared Sn@C/graphene nanocomposite as an anode material for lithium-ion batteries exhibited outstanding cyclability. The reversible specific capacity is almost constant from the tenth cycle to the fiftieth cycle, which is about 600 mA h g{sup −1}. The strategy presented in this work may be extended to improve the cycle performances of other high-capacity electrode materials with large volume variations during charge–discharge processes.

Facilely synthesized Fe2O3–graphene nanocomposite as novel electrode materials for supercapacitors with high performance

International Nuclear Information System (INIS)

Wang, Zhuo; Ma, Chunyan; Wang, Hailin; Liu, Zonghuai; Hao, Zhengping

2013-01-01

Graphical abstract: Fe 2 O 3 Graphene nanocomposite was synthesized in a simple hydrothermal way by using urea to adjust the system pH value, by this method the reduction of graphite oxide and the formation of Fe 2 O 3 nanocomposite are finished in one step. The specific capacitance of the Fe 2 O 3 Graphene electrode reached 226 F/g at a discharge current density of 1 A g –1 . Highlights: ► The Fe 2 O 3 –graphene nanocomposite was obtained by friendly method with urea in one step. ► The addition of Fe 2 O 3 composites has positive effect on the electrical performance of the graphene nanosheets. ► The specific capacitance of the Fe 2 O 3 –graphene electrode was 226 F/g at a discharge current density of 1 A g −1 . -- Abstract: Fe 2 O 3 –graphene nanocomposite with high capacitive properties had been prepared friendly and facilely by hydrothermal method in one-step. The morphology and structure of the obtained material were examined by X-ray diffraction (XRD), Brunauer–Emmett–Teller (BET) and transmission electron microscope (TEM) techniques. It was revealed by TEM images that Fe 2 O 3 nanoparticles grow well on the surface of graphene and the formation of Fe 2 O 3 nanoparticles hinders the aggregation of graphene (reduced graphene oxide, namely, RGO). Electrochemical properties of the synthesized materials were characterized by serials of electrochemical measurements in 1 M Na 2 SO 4 electrolyte. Fe 2 O 3 –graphene nanocomposite electrode show higher specific capacitance than graphene, indicating an accelerative effect of Fe 2 O 3 and graphene on improving the electrochemical performance of the electrode. The specific capacitance of Fe 2 O 3 –graphene nanocomposite is 226 F/g at a current density of 1 A/g. These attractive results indicate it is possible to seek and develop the promising, environmentally benign and commercial electrodes material based on Fe 2 O 3 and graphene

Manufacturing process for electrodes for ionizing radiation detectors

International Nuclear Information System (INIS)

Tirelli, M.G.; Hecquet, R.

1987-01-01

A manufacturing proces for electrodes for ionizing radiation detectors, particularly electrodes for X-ray multidetectors, is proposed. It consists of electrodepositing at least one layer of an electrically conducting material on at least one side of a relatively flat plate. A ductile material is used to form the conducting layer. The assembly formed by the plate covered by the ductile conducting material is subjected to pressing to crush the ductile conducting material at least in the zones where the assembly formed by the plate and the covering material has a total thickness superior to a constant thickness desired for the electrode [fr

Dilute NiO/carbon nanofiber composites derived from metal organic framework fibers as electrode materials for supercapacitors

Energy Technology Data Exchange (ETDEWEB)

Yang, Ying; Yang, Feng; Hu, Hongru; Lee, Sungsik; Wang, Yue; Zhao, Hairui; Zeng, Dehong; Zhou, Biao; Hao, Shijie

2017-01-01

A new type of carbon nanofiber (CNF) dominated electrode materials decorated with dilute NiO particles (NiO/CNF) has been in situ fabricated by direct pyrolysis of Ni, Zn-containing metal organic framework fibers, which are skillfully constructed by assembling different proportional NiCl2·6H2O and Zn(Ac)2·2H2O with trimesic acid in the presence of N,N-dimethylformamide. With elegant combination of advantages of CNF and evenly dispersed NiO particles, as well as successful modulation of conductivity and porosity of final composites, our NiO/CNF composites display well-defined capacitive features. A high capacitance of 14926 F g–1 was obtained in 6 M KOH electrolyte when the contribution from 0.43 wt% NiO was considered alone, contributing to over 35% of the total capacitance (234 F g–1 ). This significantly exceeds its theoretical specific capacitance of 2584 F g–1. It has been established from the Ragone plot that a largest energy density of 33.4 Wh kg–1 was obtained at the current density of 0.25 A g–1. Furthermore, such composite electrode materials show good rate capability and outstanding cycling stability up to 5000 times (only 10% loss). The present study provides a brand-new approach to design a high capacitance and stable supercapacitor electrode and the concept is extendable to other composite materials. Keywords: Metal organic framework; Nickel oxide; Carbon nanofiber; In situ synthesis; Capacitance

Lithium-aluminum-magnesium electrode composition

Science.gov (United States)

Melendres, Carlos A.; Siegel, Stanley

1978-01-01

A negative electrode composition is presented for use in a secondary, high-temperature electrochemical cell. The cell also includes a molten salt electrolyte of alkali metal halides or alkaline earth metal halides and a positive electrode including a chalcogen or a metal chalcogenide as the active electrode material. The negative electrode composition includes up to 50 atom percent lithium as the active electrode constituent and a magnesium-aluminum alloy as a structural matrix. Various binary and ternary intermetallic phases of lithium, magnesium, and aluminum are formed but the electrode composition in both its charged and discharged state remains substantially free of the alpha lithium-aluminum phase and exhibits good structural integrity.

Recovery of fluoride ion selective electrode

International Nuclear Information System (INIS)

Monteiro, R.P.G.

1988-01-01

A recovery procedure of fluoride ion selective electrode based upon the body radiography of inactive electrode and introduction of suitable internal regeneration solution, is developed. The recovered electrode was tested in standard solutions of fluoride ions (10 sup5) to 10 -1M showing as good performance as the new one. The fluor determination by potentiometric measurements with selective electrode is used in nuclear fuel cycle for quality control of thorium and uranium mixed oxide pellets and pellets of uranium dioxides. (author) [pt

Method of making electrodes for electrochemical cell. [Li-Al alloy

Science.gov (United States)

Kaun, T.D.; Kilsdonk, D.J.

1981-07-29

A method is described for making an electrode for an electrochemical cell in which particulate electrode-active material is mixed with a liquid organic carrier chemically inert with respect to the electrode-active material, mixing the liquid carrier to form an extrudable slurry. The liquid carrier is present in an amount of from about 10 to about 50% by volume of the slurry, and then the carrier is removed from the slurry leaving the electrode-active material. The method is particularly suited for making a lithium-aluminum alloy negative electrode for a high-temperature cell.

Decreasing redox voltage of terephthalate-based electrode material for Li-ion battery using substituent effect

Science.gov (United States)

Lakraychi, A. E.; Dolhem, F.; Djedaïni-Pilard, F.; Thiam, A.; Frayret, C.; Becuwe, M.

2017-08-01

The preparation and assessment versus lithium of a functionalized terephthalate-based as a potential new negative electrode material for Li-ion battery is presented. Inspired from molecular modelling, a decrease in redox potential is achieved through the symmetrical adjunction of electron-donating fragments (-CH3) on the aromatic ring. While the electrochemical activity of this organic material was maximized when used as nanocomposite and without any binder, the potential is furthermore lowered by 110 mV upon functionalization, consistently with predicted value gained from DFT calculations.

Water Treatment Using Plasma Discharge with Variation of Electrode Materials

Science.gov (United States)

Chanan, N.; Kusumandari; Saraswati, T. E.

2018-03-01

This research studied water treatment using plasma discharge. Plasma generated in this study produced active species that played a role in organic compound decomposition. The plasma reactor consisted of two needle electrodes made from stainless steel, tungsten, aluminium and grafit. It placed approximately 2 mm above the solution and connected with high-AC voltage. A solution of methylene blue used as an organic solution model. Plasma treatment times were 2, 4, 6, 8 and 10 min. The absorbance, temperature and pH of the solution were measured before and after treatment using various electrodes. The best electrode used in plasma discharging for methylene blue absorbance reduction was the graphite electrode, which provided the highest degradation efficiency of 98% at 6 min of treatment time.

Solvothermal synthesis of NiAl double hydroxide microspheres on a nickel foam-graphene as an electrode material for pseudo-capacitors

International Nuclear Information System (INIS)

Momodu, Damilola; Bello, Abdulhakeem; Dangbegnon, Julien; Barzeger, Farshad; Taghizadeh, Fatimeh; Fabiane, Mopeli; Manyala, Ncholu; Johnson, A. T. Charlie

2014-01-01

In this paper, we demonstrate excellent pseudo-capacitance behavior of nickel-aluminum double hydroxide microspheres (NiAl DHM) synthesized by a facile solvothermal technique using tertbutanol as a structure-directing agent on nickel foam-graphene (NF-G) current collector as compared to use of nickel foam current collector alone. The structure and surface morphology were studied by X-ray diffraction analysis, Raman spectroscopy and scanning and transmission electron microscopies respectively. NF-G current collector was fabricated by chemical vapor deposition followed by an ex situ coating method of NiAl DHM active material which forms a composite electrode. The pseudocapacitive performance of the composite electrode was investigated by cyclic voltammetry, constant charge–discharge and electrochemical impedance spectroscopy measurements. The composite electrode with the NF-G current collector exhibits an enhanced electrochemical performance due to the presence of the conductive graphene layer on the nickel foam and gives a specific capacitance of 1252 F g −1 at a current density of 1 A g −1 and a capacitive retention of about 97% after 1000 charge–discharge cycles. This shows that these composites are promising electrode materials for energy storage devices

Facile construction of 3D graphene/MoS2 composites as advanced electrode materials for supercapacitors

Science.gov (United States)

Sun, Tianhua; Li, Zhangpeng; Liu, Xiaohong; Ma, Limin; Wang, Jinqing; Yang, Shengrong

2016-11-01

Flower-like molybdenum disulfide (MoS2) microstructures are synthesized based on three-dimensional graphene (3DG) skeleton via a simple and facile one-step hydrothermal method, aiming at constructing series of novel composite electrode materials of 3DG/MoS2 with high electrochemical performances for supercapacitors. The electrochemical properties of the samples are evaluated by cyclic voltammetry and galvanostatic charge/discharge tests. Specifically, the optimal 3DG/MoS2 composite exhibits remarkable performances with a high specific capacitance of 410 F g-1 at a current density of 1 A g-1 and an excellent cycling stability with ca. 80.3% capacitance retention after 10,000 continuous charge-discharge cycles at a high current density of 2 A g-1, making it adaptive for high-performance supercapacitors. The enhanced electrochemical performances can be ascribed to the combination of 3DG and flower-like MoS2, which provides excellent charge transfer network and electrolyte diffusion channels while effectively prevents the collapse, aggregation and morphology change of active materials during charge-discharge process. The results demonstrate that 3DG/MoS2 composite is one of the attractive electrode materials for supercapacitors.

Investigations on the effects of electrode materials on the device characteristics of ferroelectric memory thin film transistors fabricated on flexible substrates

Science.gov (United States)

Yang, Ji-Hee; Yun, Da-Jeong; Seo, Gi-Ho; Kim, Seong-Min; Yoon, Myung-Han; Yoon, Sung-Min

2018-03-01

For flexible memory device applications, we propose memory thin-film transistors using an organic ferroelectric poly(vinylidene fluoride-trifluoroethylene) [P(VDF-TrFE)] gate insulator and an amorphous In-Ga-Zn-O (a-IGZO) active channel. The effects of electrode materials and their deposition methods on the characteristics of memory devices exploiting the ferroelectric field effect were investigated for the proposed ferroelectric memory thin-film transistors (Fe-MTFTs) at flat and bending states. It was found that the plasma-induced sputtering deposition and mechanical brittleness of the indium-tin oxide (ITO) markedly degraded the ferroelectric-field-effect-driven memory window and bending characteristics of the Fe-MTFTs. The replacement of ITO electrodes with metal aluminum (Al) electrodes prepared by plasma-free thermal evaporation greatly enhanced the memory device characteristics even under bending conditions owing to their mechanical ductility. Furthermore, poly(3,4-ethylenedioxythiophene)-poly(styrene sulfonate) (PEDOT:PSS) was introduced to achieve robust bending performance under extreme mechanical stress. The Fe-MTFTs using PEDOT:PSS source/drain electrodes were successfully fabricated and showed the potential for use as flexible memory devices. The suitable choice of electrode materials employed for the Fe-MTFTs is concluded to be one of the most important control parameters for highly functional flexible Fe-MTFTs.

Bacterial-cellulose-derived carbon nanofiber@MnO₂ and nitrogen-doped carbon nanofiber electrode materials: an asymmetric supercapacitor with high energy and power density.

Science.gov (United States)

Chen, Li-Feng; Huang, Zhi-Hong; Liang, Hai-Wei; Guan, Qing-Fang; Yu, Shu-Hong

2013-09-14

A new kind of high-performance asymmetric supercapacitor is designed with pyrolyzed bacterial cellulose (p-BC)-coated MnO₂ as a positive electrode material and nitrogen-doped p-BC as a negative electrode material via an easy, efficient, large-scale, and green fabrication approach. The optimal asymmetric device possesses an excellent supercapacitive behavior with quite high energy and power density. Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Biomimetic synthesis and characterization of the positive electrode material LiFePO4

International Nuclear Information System (INIS)

Li Peng; He Wen; Zhao Hongshi; Wang Shaopeng

2009-01-01

The biosurfactant is used as the template to synthesize lithium iron phosphate (LiFePO 4 ) precursor with the co-precipitation method and the microwave sintering method is used to prepare positive electrode material LiFePO 4 for the lithium ion battery. By using the Brunauer-Emmett-Teller (BET) surface areas, X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR) and conductometer, the authors explored the influence of the microwave power on the structure and performance of the materials. The results the authors got have proved that good crystal and high conductivity values can be obtained from the LiFePO 4 powders which are processed 10 min under the microwave power of 300 W

Electrode materials: a challenge for the exploitation of protonic solid oxide fuel cells

Directory of Open Access Journals (Sweden)

Emiliana Fabbri, Daniele Pergolesi and Enrico Traversa

2010-01-01

Full Text Available High temperature proton conductor (HTPC oxides are attracting extensive attention as electrolyte materials alternative to oxygen-ion conductors for use in solid oxide fuel cells (SOFCs operating at intermediate temperatures (400–700 °C. The need to lower the operating temperature is dictated by cost reduction for SOFC pervasive use. The major stake for the deployment of this technology is the availability of electrodes able to limit polarization losses at the reduced operation temperature. This review aims to comprehensively describe the state-of-the-art anode and cathode materials that have so far been tested with HTPC oxide electrolytes, offering guidelines and possible strategies to speed up the development of protonic SOFCs.

Electrode materials: a challenge for the exploitation of protonic solid oxide fuel cells

International Nuclear Information System (INIS)

Fabbri, Emiliana; Pergolesi, Daniele; Traversa, Enrico

2010-01-01

High temperature proton conductor (HTPC) oxides are attracting extensive attention as electrolyte materials alternative to oxygen-ion conductors for use in solid oxide fuel cells (SOFCs) operating at intermediate temperatures (400-700 0 C). The need to lower the operating temperature is dictated by cost reduction for SOFC pervasive use. The major stake for the deployment of this technology is the availability of electrodes able to limit polarization losses at the reduced operation temperature. This review aims to comprehensively describe the state-of-the-art anode and cathode materials that have so far been tested with HTPC oxide electrolytes, offering guidelines and possible strategies to speed up the development of protonic SOFCs. (topical review)

S-functionalized MXenes as electrode materials for Li-ion batteries

KAUST Repository

Zhu, Jiajie

2016-09-03

MXenes are promising electrode materials for Li-ion batteries because of their high Li capacities and cycling rates. We use density functional theory to investigate the structural and energy storage properties of Li decorated Zr2C and Zr2CX2 (X = F, O and S). We find for Zr2C and Zr2CS2 high Li specific capacities and low diffusion barriers. To overcome the critical drawbacks of the OH, F, and O groups introduced during the synthesis we propose substitution by S groups and demonstrate that an exchange reaction is indeed possible. Zr2CS2 shows a similar Li specific capacity as Zr2CO2 but a substantially reduced diffusion barrier. © 2016 Elsevier Ltd

Results of the research on electrode and insulation wall material in fiscal 1977. Large scale technological development 'R and D on magneto hydrodynamic generation'; 1977 nendo denkyoku oyobi zetsuenheki zairyo ni kansuru kenkyu seika

Energy Technology Data Exchange (ETDEWEB)

NONE

1978-06-01

Results of research in fiscal 1977 were compiled concerning electrodes and insulation wall materials, the research conducted by the material working group of the magneto hydrodynamic (MHD) generation R and D liaison conference. Researches on trial manufacturing of duct materials for MHD generation were conducted for a Si{sub 3}N{sub 4}-MgO, Si{sub 3}N{sub 4}-Spinel, Spinel and Sialon based insulation wall material, MgO-BN based insulation wall material, tin oxide based electrode material, cold press ZrO{sub 2}-CeO{sub 2} and ZrO{sub 2}-Y{sub 2}O{sub 2} based electrode material, hot press hot hydrostatic pressure ZrO{sub 2}-CeO{sub 2} based electrode material, cermet based electrode material, etc. In the investigation and measurement of basic characteristics, these materials were put through various tests such as 1,300 degree C-300 hr-K{sub 2}SO{sub 4} immersion test, thermal shock resistance, thermal expansibility, oxidation resistance of oxide/nitride based materials. In addition, selection of materials for MHD generation, as well as the examination and degradation analysis of dynamic characteristics, was carried out by simulation of MHD generation, which provided data of various electrodes such as consumption, electrical characteristics (electrode lowering voltage, critical current, etc.) and thermal characteristics (surface temperature, heat flow velocity, etc.) (NEDO)

Al-Doped ZnO Monolayer as a Promising Transparent Electrode Material: A First-Principles Study

Directory of Open Access Journals (Sweden)

Mingyang Wu

2017-03-01

Full Text Available Al-doped ZnO has attracted much attention as a transparent electrode. The graphene-like ZnO monolayer as a two-dimensional nanostructure material shows exceptional properties compared to bulk ZnO. Here, through first-principle calculations, we found that the transparency in the visible light region of Al-doped ZnO monolayer is significantly enhanced compared to the bulk counterpart. In particular, the 12.5 at% Al-doped ZnO monolayer exhibits the highest visible transmittance of above 99%. Further, the electrical conductivity of the ZnO monolayer is enhanced as a result of Al doping, which also occurred in the bulk system. Our results suggest that Al-doped ZnO monolayer is a promising transparent conducting electrode for nanoscale optoelectronic device applications.

Binder free MnO2/PIn electrode material for supercapacitor application

Science.gov (United States)

Purty, B.; Choudhary, R. B.; Kandulna, R.; Singh, R.

2018-05-01

Electrochemically stable MnO2/PIn nanocomposite was synthesized via in-situ chemical oxidative polymerization process. The structural and morphological properties were studied through FTIR and FESEM characterizing techniques. Sphere like PIn and MnO2 nanorods offers interacting surface for charge transfer action. The electrochemical properties were investigated through cyclic voltammetry (CV), galvanostatic charge-discharge (GCD) and electrochemical impedance spectroscopic (EIS) techniques. The significant enhancement in capacitance value with 95% coulombic efficiency and relatively low equivalent series resistance (ESR)˜0.4 Ω proved that MnO2/PIn nanocomposite is an excellent performer as an electrode material in the spectrum of supercapcitors and optoelectronic devices.

Nitrogen and sulfur co-doped porous graphene aerogel as an efficient electrode material for high performance supercapacitor in ionic liquid electrolyte

Science.gov (United States)

Chen, Yujuan; Liu, Zhaoen; Sun, Li; Lu, Zhiwei; Zhuo, Kelei

2018-06-01

Nitrogen and sulfur co-doped graphene aerogel (NS-GA) is prepared by one-pot process. The as-prepared materials are investigated as supercapacitors electrodes in an ionic liquid (1-ethyl-3-methylimidazolium tetrafluoroborate, EMIMBF4) electrolyte. The NS-GA is characterized using X-ray diffraction, X-ray photoelectron spectroscopy, and Raman spectroscopy scanning electron microscopy. The results show that the NS-GA has hierarchical porous structure. Electrochemical performance is investigated by cycle voltammetry and galvanostatic charge-discharge. Notably, the supercapacitor based on the NS-GA-5 possesses a maximum energy density of 100.7 Wh kg-1 at power density of 0.94 kW kg-1. The electrode materials also offer a large specific capacitance of 203.2 F g-1 at a current density of 1 A g-1 and the capacitance retention of NS-GA-5 is 90% after 3000 cycles at a scan rate of 2 A g-1. The NS-GA-5 with numerous advantages including low cost and remarkable electrochemical behaviors can be a promising electrode material for the application of supercapacitors.

Conducting polymer coated neural recording electrodes

Science.gov (United States)

Harris, Alexander R.; Morgan, Simeon J.; Chen, Jun; Kapsa, Robert M. I.; Wallace, Gordon G.; Paolini, Antonio G.

2013-02-01

Objective. Neural recording electrodes suffer from poor signal to noise ratio, charge density, biostability and biocompatibility. This paper investigates the ability of conducting polymer coated electrodes to record acute neural response in a systematic manner, allowing in depth comparison of electrochemical and electrophysiological response. Approach. Polypyrrole (Ppy) and poly-3,4-ethylenedioxythiophene (PEDOT) doped with sulphate (SO4) or para-toluene sulfonate (pTS) were used to coat iridium neural recording electrodes. Detailed electrochemical and electrophysiological investigations were undertaken to compare the effect of these materials on acute in vivo recording. Main results. A range of charge density and impedance responses were seen with each respectively doped conducting polymer. All coatings produced greater charge density than uncoated electrodes, while PEDOT-pTS, PEDOT-SO4 and Ppy-SO4 possessed lower impedance values at 1 kHz than uncoated electrodes. Charge density increased with PEDOT-pTS thickness and impedance at 1 kHz was reduced with deposition times up to 45 s. Stable electrochemical response after acute implantation inferred biostability of PEDOT-pTS coated electrodes while other electrode materials had variable impedance and/or charge density after implantation indicative of a protein fouling layer forming on the electrode surface. Recording of neural response to white noise bursts after implantation of conducting polymer-coated electrodes into a rat model inferior colliculus showed a general decrease in background noise and increase in signal to noise ratio and spike count with reduced impedance at 1 kHz, regardless of the specific electrode coating, compared to uncoated electrodes. A 45 s PEDOT-pTS deposition time yielded the highest signal to noise ratio and spike count. Significance. A method for comparing recording electrode materials has been demonstrated with doped conducting polymers. PEDOT-pTS showed remarkable low fouling during

Characteristics of Carbon Nanotubes/Graphene Coatings on Stainless Steel Meshes Used as Electrodes for Air-Cathode Microbial Fuel Cells

Directory of Open Access Journals (Sweden)

Wei-Hsuan Hsu

2017-01-01

Full Text Available Microbial fuel cells (MFCs generate low-pollution power by feeding organic matter to bacteria; MFC applications have become crucial for energy recovery and environmental protection. The electrode materials of any MFC affect its power generation capacity. In this research, nine single-chamber MFCs with various electrode configurations were investigated and compared with each other. A fabrication process for carbon-based electrode coatings was proposed, and Escherichia coli HB101 was used in the studied MFC system. The results show that applying a coat of either graphene or carbon nanotubes (CNTs to a stainless steel mesh electrode can improve the power density and reduce the internal resistance of an MFC system. Using the proposed surface modification method, CNTs and graphene used for anodic and cathodic modification can increase power generation by approximately 3–7 and 1.5–4.5 times, respectively. Remarkably, compared to a standard MFC with an untreated anode, the internal resistances of MFCs with CNTs- and graphene-modified anodes were reduced to 18 and 30% of standard internal resistance. Measurements of the nine systems we studied clearly presented the performance levels of CNTs and graphene applied as surface modification of stainless steel mesh electrodes.

Modified Gold Electrode and Hollow Mn3O4 Nanoparticles as Electrode Materials for Microbial Fuel Cell Applications

Science.gov (United States)

Dhungana, Pramod

Microbial fuel cell (MFC) technology has attracted great attention in the scientific community as it offers the possibility of extraction of electricity from wide range of soluble and dissolved organic waste or renewable biomass, including sludge, waste water and cellulosic biomass. Microbial fuel cells are devices that utilize microbial metabolic processes to convert chemical energy via the oxidation of organic substances to produce electric current. MFCs consist of two chambers, an anode and cathode, separated by ion-permeable materials. The efficiency of producing electricity using the MFC depends on several factors such as immobilization of microorganisms on anode, mode of electron transfer, types of substrate/fuel and effectiveness of cathode materials for oxygen reduction reaction (ORR). In this work, in order to immobilize the microorganisms on anode materials, we have investigated the surface modification of gold electrode (anode) using alkyl dithiol and aryl thiol with glucose. The modification processes were characterized by using contact angle measurements and proton nuclear magnetic resonance (NMR). In order to study the effectiveness of cathode materials for ORR, we have synthesized hollow Mn3O 4 nanoparticles which are electrically very poor. Therefore, the hollow nanoparticles were mixed with electrically conductive multi-walled carbon nanotube as support and optimized the mixing process. This composite material shows enhanced ORR activity in all types of pH conditions. In future, we will focus to integrate anode and cathode in MFC to check its efficiency to produce electricity.

Uncharged positive electrode composition

Science.gov (United States)

Kaun, Thomas D.; Vissers, Donald R.; Shimotake, Hiroshi

1977-03-08

An uncharged positive-electrode composition contains particulate lithium sulfide, another alkali metal or alkaline earth metal compound other than sulfide, e.g., lithium carbide, and a transition metal powder. The composition along with a binder, such as electrolytic salt or a thermosetting resin is applied onto an electrically conductive substrate to form a plaque. The plaque is assembled as a positive electrode within an electrochemical cell opposite to a negative electrode containing a material such as aluminum or silicon for alloying with lithium. During charging, lithium alloy is formed within the negative electrode and transition metal sulfide such as iron sulfide is produced within the positive electrode. Excess negative electrode capacity over that from the transition metal sulfide is provided due to the electrochemical reaction of the other than sulfide alkali metal or alkaline earth metal compound.

VS4 Nanoparticles Anchored on Graphene Sheets as a High-Rate and Stable Electrode Material for Sodium Ion Batteries.

Science.gov (United States)

Pang, Qiang; Zhao, Yingying; Yu, Yanhao; Bian, Xiaofei; Wang, Xudong; Wei, Yingjin; Gao, Yu; Chen, Gang

2018-02-22

The size and conductivity of the electrode materials play a significant role in the kinetics of sodium-ion batteries. Various characterizations reveal that size-controllable VS 4 nanoparticles can be successfully anchored on the surface of graphene sheets (GSs) by a simple cationic-surfactant-assisted hydrothermal method. When used as an electrode material for sodium-ion batteries, these VS 4 @GS nanocomposites show large specific capacity (349.1 mAh g -1 after 100 cycles), excellent long-term stability (84 % capacity retention after 1200 cycles), and high rate capability (188.1 mAh g -1 at 4000 mA g -1 ). A large proportion of the capacity was contributed by capacitive processes. This remarkable electrochemical performance was attributed to synergistic interactions between nanosized VS 4 particles and a highly conductive graphene network, which provided short diffusion pathways for Na + ions and large contact areas between the electrolyte and electrode, resulting in considerably improved electrochemical kinetic properties. © 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Evaluation of Niobium as Candidate Electrode Material for DC High Voltage Photoelectron Guns

Science.gov (United States)

BastaniNejad, M.; Mohamed, Abdullah; Elmustafa, A. A.; Adderley, P.; Clark, J.; Covert, S.; Hansknecht, J.; Hernandez-Garcia, C.; Poelker, M.; Mammei, R.;

Electron transfer reactions to probe the electrode/solution interface

Energy Technology Data Exchange (ETDEWEB)

Capitanio, F.; Guerrini, E.; Colombo, A.; Trasatti, S. [Milan Univ., Milan (Italy). Dept. of Physical Chemistry and Electrochemistry

2008-07-01

The reactions that occur at the interface between an electrode and an electrolyte were examined with particular reference to the interaction of different electrode surfaces with redox couples. A semi-integration or convolution technique was used to study the kinetics of electron transfer on different electrode materials with different hydrophilic behaviour, such as Boron-Doped-Diamond (BDD), Au and Pt. Standard reversible redox couples were also investigated, including (Fe3+/2+, Fe(CN)63-/4-, Ru(NH3)63+/2+, Co(NH3)63+/2+, Ir4+/3+, V4+/5+ and V3+/2+). The proposed method proved to be simple, straightforward and reliable since the obtained kinetic information was in good agreement with data in the literature. It was concluded that the kinetics of the electrode transfer reactions depend on the chemical nature of the redox couple and electrode material. The method should be further extended to irreversible couples and other electrode materials such as mixed oxide electrodes. 3 refs., 2 figs.

Colloidal paradigm in supercapattery electrode systems

Science.gov (United States)

Chen, Kunfeng; Xue, Dongfeng

2018-01-01

Among decades of development, electrochemical energy storage systems are now sorely in need of a new design paradigm at the nano size and ion level to satisfy the higher energy and power demands. In this review paper, we introduce a new colloidal electrode paradigm for supercapattery that integrates multiple-scale forms of matter, i.e. ion clusters, colloidal ions, and nanosized materials, into one colloid system, coupled with multiple interactions, i.e. electrostatic, van der Waals forces, and chemical bonding, thus leading to the formation of many redox reactive centers. This colloidal electrode not only keeps the original ionic nature in colloidal materials, but also creates a new attribute of high electroactivity. Colloidal supercapattery is a perfect application example of the novel colloidal electrode, leading to higher specific capacitance than traditional electrode materials. The high electroactivity of the colloidal electrode mainly comes from the contribution of exposed reactive centers, owing to the confinement effect of carbon and a binder matrix. Systematic and thorough research on the colloidal system will significantly promote the development of fundamental science and the progress of advanced energy storage technology.

Positive electrode for a lithium battery

Science.gov (United States)

Park, Sang-Ho; Amine, Khalil

2015-04-07

A method for producing a lithium alkali transition metal oxide for use as a positive electrode material for lithium secondary batteries by a precipitation method. The positive electrode material is a lithium alkali transition metal composite oxide and is prepared by mixing a solid state mixed with alkali and transition metal carbonate and a lithium source. The mixture is thermally treated to obtain a small amount of alkali metal residual in the lithium transition metal composite oxide cathode material.

Effects of ion implantation on the electrochemical characteristics of carbon electrodes

International Nuclear Information System (INIS)

Takahashi, Katsuo; Iwaki, Masaya

1994-01-01

Various carbon materials are important electrode materials for electrochemical field. By ion implantation, the surface layer reforming of carbon materials (mainly galssy carbon) was carried out, and the effect that it exerts to their electrode characteristics was investigated. As the results of the ion implantation of Li, N, O, K, Ti, Zn, Cd and others performed so far, it was found that mainly by the change of the surface layer to amorphous state, there were the effects of the lowering of base current and the lowering of electrode reaction rate, and it was known that the surface layers of carbon materials doped with various kinds of ions showed high chemical stability. The use of carbon materials as electrodes in electrochemistry is roughly divided into the electrodes for electrolytic industry and fuel cells for large current and those for the measurement in electrochemical reaction for small current. The structure of carbon materials and electrode characteristics, and the reforming effect by ion implantation are reported. (K.I.)

Helium Ion Microscopy of proton exchange membrane fuel cell electrode structures

Directory of Open Access Journals (Sweden)

Serguei Chiriaev

2017-12-01

Full Text Available Characterization of composite materials with microscopy techniques is an essential route to understanding their properties and degradation mechanisms, though the observation with a suitable type of microscopy is not always possible. In this work, we present proton exchange membrane fuel cell electrode interface structure dependence on ionomer content, systematically studied by Helium Ion Microscopy (HIM. A special focus was on acquiring high resolution images of the electrode structure and avoiding interface damage from irradiation and tedious sample preparation. HIM demonstrated its advantages in surface imaging, which is paramount in studies of the interface morphology of ionomer covered or absorbed catalyst structures in a combination with electrochemical characterization and accelerated stress test. The electrode porosity was found to depend on the ionomer content. The stressed electrodes demonstrated higher porosity in comparison to the unstressed ones on the condition of no external mechanical pressure. Moreover, formation of additional small grains was observed for the electrodes with the low ionomer content, indicating Pt redeposition through Ostwald ripening. Polymer nanofiber structures were found in the crack regions of the catalyst layer, which appear due to the internal stress originated from the solvent evaporation. These fibers have fairly uniform diameters of a few tens of nanometers, and their density increases with the increasing ionomer content in the electrodes. In the hot-pressed electrodes, we found more closed contact between the electrode components, reduced particle size, polymer coalescence and formation of nano-sized polymer fiber architecture between the particles.

Lithium battery electrodes with ultra-thin alumina coatings

Science.gov (United States)

Se-Hee, Lee; George, Steven M.; Cavanagh, Andrew S.; Yoon Seok, Jung; Dillon, Anne C.

2015-11-24

Electrodes for lithium batteries are coated via an atomic layer deposition process. The coatings can be applied to the assembled electrodes, or in some cases to particles of electrode material prior to assembling the particles into an electrode. The coatings can be as thin as 2 .ANG.ngstroms thick. The coating provides for a stable electrode. Batteries containing the electrodes tend to exhibit high cycling capacities.

Microwave-assisted ionothermal synthesis of nanostructured anatase titanium dioxide/activated carbon composite as electrode material for capacitive deionization

International Nuclear Information System (INIS)

Liu, Po-I; Chung, Li-Ching; Shao, Hsin; Liang, Teh-Ming; Horng, Ren-Yang; Ma, Chen-Chi M.; Chang, Min-Chao

2013-01-01

The nanostructured anatase titanium dioxide/activated carbon composite material for capacitive deionization electrode was prepared in a short time by a lower temperature two-step microwave-assisted ionothermal (sol–gel method in the presence of ionic liquid) synthesis method. This method includes a reaction and a crystallization step. In the crystallization step, the ionic liquid plays a hydrothermal analogy role in driving the surface anatase crystallization of amorphous titanium dioxide nanoparticles formed in the reaction step. The energy dispersive spectroscopic study of the composite indicates that the anatase titanium dioxide nanoparticles are evenly deposited in the matrix of activated carbon. The electrochemical property of the composite electrode was investigated. In comparison to the pristine activated carbon electrode, higher specific capacitance was observed for the nanostructured anatase titanium dioxide/activated carbon composite electrode, especially when the composite was prepared with a molar ratio of titanium tetraisopropoxide/H 2 O equal to 1:15. Its X-ray photoelectron spectroscopic result indicates that it has the highest amount of Ti-OH. The Ti-OH group can enhance the wetting ability and the specific capacitance of the composite electrode. The accompanying capacitive deionization result indicates that the decay of electrosorption capacity of this composite electrode is insignificant after five cycle tests. It means that the ion electrosorption–desorption becomes a reversible process

Achievement report for fiscal 1976 on research in materials for electrodes and insulation walls. Large-scale technology development (Research and development of magnetohydrodynamic power generation); 1976 nendo denkyoku oyobi zetsuenheki zairyo ni kansuru kenkyu seika

Energy Technology Data Exchange (ETDEWEB)

NONE

1977-06-01

This report covers the achievements attained in fiscal 1976 by the materials working group engaged in the study of materials for electrodes and insulation walls. Fabricated and tested in the study relative to the experimental fabrication of materials for magnetohydrodynamic (MHD) power generation are MgO-Si{sub 3}N{sub 4} based insulation materials, MgO-BN based insulation materials, tin oxide based electrode materials, ZrO{sub 2}-CeO{sub 2} based cold pressed electrode materials, cermet based electrode materials, etc. In the research on basic characteristics and measurement, various electrode materials and insulation wall materials are subjected to a 300-hour K{sub 2}SO{sub 4} corrosion test at 1,300 degrees C. In the simulation of MHD power generation, correlations are investigated between materials, cooling structures, and dynamic characteristics, and data are collected to enable the prediction of performance and consumption of the materials during power generation. A data processing system is developed for the said simulation, and this enhances experimenting efficiency. In the study of insulation wall structures and electrode phenomena, studies are conducted about the thermal stress in power generation duct wall materials, localized anomalous heating due to arc spots, and the transfer of heat between the power generation duct wall materials and the cooling material. (NEDO)

Electrode Materials, Thermal Annealing Sequences, and Lateral/Vertical Phase Separation of Polymer Solar Cells from Multiscale Molecular Simulations

KAUST Repository

Lee, Cheng-Kuang; Wodo, Olga; Ganapathysubramanian, Baskar; Pao, Chun-Wei

2014-01-01

. Simulations are performed for various configurations of electrode materials as well as processing temperature. The complex CG molecular data are characterized using a novel extension of our graph-based framework to quantify morphology and establish a link

Characterization of textile electrodes and conductors using standardized measurement setups

International Nuclear Information System (INIS)

Beckmann, L; Neuhaus, C; Medrano, G; Walter, M; Leonhardt, S; Jungbecker, N; Gries, T

2010-01-01

Textile electrodes and conductors are being developed and used in different monitoring scenarios, such as ECG or bioimpedance spectroscopy measurements. Compared to standard materials, conductive textile materials offer improved wearing comfort and enable long-term measurements. Unfortunately, the development and investigation of such materials often suffers from the non-reproducibility of the test scenarios. For example, the materials are generally tested on human skin which is difficult since the properties of human skin differ for each person and can change within hours. This study presents two test setups which offer reproducible measurement procedures for the systematic analysis of textile electrodes and conductors. The electrode test setup was designed with a special skin dummy which allows investigation of not only the electrical properties of textile electrodes but also the contact behavior between electrode and skin. Using both test setups, eight textile electrodes and five textile conductors were analyzed and compared

Evaluation of niobium as candidate electrode material for dc high voltage photoelectron guns

Directory of Open Access Journals (Sweden)

M. BastaniNejad

2012-08-01

Full Text Available The field emission characteristics of niobium electrodes were compared to those of stainless steel electrodes using a DC high voltage field emission test apparatus. A total of eight electrodes were evaluated: two 304 stainless steel electrodes polished to mirrorlike finish with diamond grit and six niobium electrodes (two single-crystal, two large-grain, and two fine-grain that were chemically polished using a buffered-chemical acid solution. Upon the first application of high voltage, the best large-grain and single-crystal niobium electrodes performed better than the best stainless steel electrodes, exhibiting less field emission at comparable voltage and field strength. In all cases, field emission from electrodes (stainless steel and/or niobium could be significantly reduced and sometimes completely eliminated, by introducing krypton gas into the vacuum chamber while the electrode was biased at high voltage. Of all the electrodes tested, a large-grain niobium electrode performed the best, exhibiting no measurable field emission (<10  pA at 225 kV with 20 mm cathode/anode gap, corresponding to a field strength of 18.7  MV/m.

Experimental study of the electrode material for electro-osmosis in mudflat sludge

Science.gov (United States)

Liu, Yi-min; Xu, Hao-feng

2017-11-01

In order to study the performance of electro-osmosis, several tests including indoor electro-osmosis experiments using copper, aluminum as the anode and cathode electrode materials, and Mercury Intrusion Porosimiter (MIP) were conducted. The results indicate that the drainage ratio using aluminum is faster than that of copper while the energy consumption per unit is lower, the effectiveness is better than that of copper. After electro-osmosis, the percentage of pore with large diameter shows a remarkable decrease comparing with the remolded soil which result in the increase of pore with small diameter. The reasons were discussed in this paper.

Mesoporous MnO2/carbon aerogel composites as promising electrode materials for high-performance supercapacitors.

Science.gov (United States)

Li, Gao-Ren; Feng, Zhan-Ping; Ou, Yan-Nan; Wu, Dingcai; Fu, Ruowen; Tong, Ye-Xiang

2010-02-16

MnO(2) as one of the most promising candidates for electrochemical supercapacitors has attracted much attention because of its superior electrochemical performance, low cost, and environmentally benign nature. In this Letter, we explored a novel route to prepare mesoporous MnO(2)/carbon aerogel composites by electrochemical deposition assisted by gas bubbles. The products were characterized by energy-dispersive spectrometry (EDS), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). The MnO(2) deposits are found to have high purity and have a mesoporous structure that will optimize the electronic and ionic conductivity to minimize the total resistance of the system and thereby maximize the performance characteristics of this material for use in supercapacitor electrodes. The results of nitrogen adsorption-desorption experiments and electrochemical measurements showed that these obtained mesoporous MnO(2)/carbon aerogel composites had a large specific surface area (120 m(2)/g), uniform pore-size distribution (around 5 nm), high specific capacitance (515.5 F/g), and good stability over 1000 cycles, which give these composites potential application as high-performance supercapacitor electrode materials.

Supercapacitor Electrode Materials from Highly Porous Carbon Nanofibers with Tailored Pore Distributions

Science.gov (United States)

Chathurika Abeykoon, Nimali

Environmental and human health risks associated with the traditional methods of energy production (e.g., oil and gas) and intermittency and uncertainty of renewable sources (e.g., solar and wind) have led to exploring effective and alternative energy sources to meet the growing energy demands. Electricity based on energy storage devices are the most promising solutions for realization of these objectives. Among the energy storage devices, electrochemical double layer capacitors (EDLCs) or supercapacitors have become an attractive research interest due to their outstanding performance, especially high power densities, long cycle life and rapid charge and discharge times, which enables them to utilize in many applications including consumer electronics and transportation, where high power is needed. However, low energy density of supercapacitors is a major obstacle to compete with the commercially existing high energy density energy storage device such as batteries. The fabrication of advanced electrodes materials with very high surface area from novel precursors and utilization of electrolytes with higher operating voltages are essential to enhance energy density of supercapacitors. In this work, carbon nanofibers (CNFs) from different polymer precursors with new fabrication techniques are explored to develop highly porous carbon with tailored pore distributions to match with employed ionic liquid electrolytes (which possess high working voltages), to realize high energy storage capability. Novel electrode materials derived from electrospun immiscible polymer blends and synthesized copolymers and terpolymers were described. Pore distributions of CNFs were tailored by varying the composition of polymers in immiscible blends or varying the monomer ratios of copolymer or terpolymers. Chapter 1 gives the detailed introduction of supercapacitors including history and storage principle of EDLCs, fabrication of carbon nanofiber based electrodes and electrolytes employed

Activation and discharge kinetics of metal hydride electrodes

Energy Technology Data Exchange (ETDEWEB)

Johnsen, Stein Egil

2003-07-01

Potential step chronoamperometry and Electrochemical Impedance Spectroscopy (eis) measurements were performed on single metal hydride particles. For the {alpha}-phase, the bulk diffusion coefficient and the absorption/adsorption rate parameters were determined. Materials produced by atomisation, melt spinning and conventional casting were investigated. The melt spun and conventional cast materials were identical and the atomised material similar in composition. The particles from the cast and the melt spun material were shaped like parallelepipeds. A corresponding equation, for this geometry, for diffusion coupled to an absorption/adsorption reaction was developed. It was found that materials produced by melt spinning exhibited lower bulk diffusion (1.7E-14 m2/s) and absorption/adsorption reaction rate (1.0E-8 m/s), compared to materials produced by conventionally casting (1.1E-13 m2/s and 5.5E-8 m/s respectively). In addition, the influence of particle active surface and relative diffusion length were discussed. It was concluded that there are uncertainties connected to these properties, which may explain the large distribution in the kinetic parameters measured on metal hydride particles. Activation of metal hydride forming materials has been studied and an activation procedure, for porous electrodes, was investigated. Cathodic polarisation of the electrode during a hot alkaline surface treatment gave the maximum discharge capacity on the first discharge of the electrode. The studied materials were produced by gas atomisation and the spherical shape was retained during the activation. Both an AB{sub 5} and an AB{sub 2} alloy was successfully activated and discharge rate properties determined. The AB{sub 2} material showed a higher maximum discharge capacity, but poor rate properties, compared to the AB{sub 5} material. Reduction of surface oxides, and at the same time protection against corrosion of active metallic nickel, can explain the satisfying results of

Variations the diameter tip of electrode on the resistance spot welding using electrode Cu on worksheet Fe

Science.gov (United States)

Baskoro, A. S.; Sugeng, S.; Sifa, Agus; Badruzzaman; Endramawan, Tito

2018-04-01

Resistance Spot Weld (RSW) is a welding technology which plays an important role that is often used in industry in large manufacturing industries, especially in the automotive sector, some of the parameters are affecting the welding process that give impact in the weld quality, diameter tip important impact on the resistance spot welding, This study can be categorized as experimental study by using Electrode material such as Cu and Fe Worksheet Materials, with a material thickness of 1 mm,0,8 mm, and 0,6 mm on each worksheet, and the large diameter of tip electrode (5√t) depend on the thickness of worksheet. Testing the material in the electrode and the worksheet by testing the composition and tensile test, and the hardness of the material used are to know the material used certainly. The result of the welding process was done by using the parameters voltage of 8KV, with a duty cycle of 50% using a variation of the time 8s-10s, and variations the electrode tip diameter that are affected by the thickness of the worksheet 5\\sqrt{t}, plate thickness used 1 mm, 0,8 mm and 0,6 mm, so that the electrodes was used to a thickness of 1 mm diameter tip electrode 5 mm, thickness 0,8 mm with an electrode tip diameter 4,5 mm and a thickness 0,6 mm with an electrode diameter of 4 mm, with current welding parameter 8kVA, and variations in holding time 10s, 9s and 8s 50% duty cycle, then testing welds with the standard shear test refers ASTM A370-2012 with more results to a thickness of 0,6 has the ability to withstand greater load on the holding time 8s and 9s, 10s, to a thickness 0,8 mm and 1 mm shear test results demonstrate the ability to withstand loads on the holding time of 10s and 9s have a greater ability than 8s on worksheet that has thickness 1 mm at a holding time of 10s, and then Maximum shear test averaging of 36,41 N at a worksheet with a thickness of 0,8 mm (diameter tip 4,5 mm) at a holding time of 8s and a mean minimum shear stress of 23,73 N at worksheet that

Au-embedded ZnO/NiO hybrid with excellent electrochemical performance as advanced electrode materials for supercapacitor.

Science.gov (United States)

Zheng, Xin; Yan, Xiaoqin; Sun, Yihui; Bai, Zhiming; Zhang, Guangjie; Shen, Yanwei; Liang, Qijie; Zhang, Yue

2015-02-04

Here we design a nanostructure by embedding Au nanoparticles into ZnO/NiO core-shell composites as supercapacitors electrodes materials. This optimized hybrid electrodes exhibited an excellent electrochemical performance including a long-term cycling stability and a maximum specific areal capacitance of 4.1 F/cm(2) at a current density of 5 mA/cm(2), which is much higher than that of ZnO/NiO hierarchical materials (0.5 F/cm(2)). Such an enhanced property is attributed to the increased electro-electrolyte interfaces, short electron diffusion pathways and good electrical conductivity. Apart from this, electrons can be temporarily trapped and accumulated at the Fermi level (EF') because of the localized schottky barrier at Au/NiO interface in charge process until fill the gap between ZnO and NiO, so that additional electrons can be released during discharge. These results demonstrate that suitable interface engineering may open up new opportunities in the development of high-performance supercapacitors.

A fundamental approach to better understand the lithium insertion mechanisms in electrode materials; Une approche fondamentale pour mieux comprendre les mecanismes d`insertion du lithium dans les materiaux d`electrodes

Energy Technology Data Exchange (ETDEWEB)

Olivier-Fourcade, J.; Branci, C.; Sarradin, J.; Jumas, J.C. [Montpellier-2 Univ., 34 (France). Laboratoire de Physicochimie de la Matiere Condensee

1996-12-31

The development of rechargeable lithium batteries with a high mass capacity, made with non-toxic and low cost materials is an important industrial challenge. Morphological and structural modifications occurring in the electrode materials during charge-output cycles should not lower the electrochemical characteristics and the cycling properties of the battery. Thus the structure of electrode materials must be sufficiently deformable and stable to support the constraints linked with lithium intercalation and de-intercalation (ions and electrons absorption/extraction). The aim of this work is to explain some characteristics (mass capacity, ions and electrons mobility, cycling) using the relation between some mechanisms of lithium insertion (sites occupation, lattice reduction mods) and the nature of atoms and chemical bonds (covalence, ionicity). This approach is developed on 2-D models of crystallized and vitreous sulfur compounds (CdI{sub 2} type) with a large inter-sheet distance, and on 3-D spinel models with a huge number of vacant sites. The method is based on a correlation between experimental studies (XAFS, DX, Moessbauer, XPS) and theoretical calculations and on the electronic and electrochemical characteristics. The model proposed should allow to improve materials in a predictive way (type of substitution) or to imagine new materials. (J.S.) 15 refs.

A fundamental approach to better understand the lithium insertion mechanisms in electrode materials; Une approche fondamentale pour mieux comprendre les mecanismes d`insertion du lithium dans les materiaux d`electrodes

Energy Technology Data Exchange (ETDEWEB)

Olivier-Fourcade, J; Branci, C; Sarradin, J; Jumas, J C [Montpellier-2 Univ., 34 (France). Laboratoire de Physicochimie de la Matiere Condensee

1997-12-31

The development of rechargeable lithium batteries with a high mass capacity, made with non-toxic and low cost materials is an important industrial challenge. Morphological and structural modifications occurring in the electrode materials during charge-output cycles should not lower the electrochemical characteristics and the cycling properties of the battery. Thus the structure of electrode materials must be sufficiently deformable and stable to support the constraints linked with lithium intercalation and de-intercalation (ions and electrons absorption/extraction). The aim of this work is to explain some characteristics (mass capacity, ions and electrons mobility, cycling) using the relation between some mechanisms of lithium insertion (sites occupation, lattice reduction mods) and the nature of atoms and chemical bonds (covalence, ionicity). This approach is developed on 2-D models of crystallized and vitreous sulfur compounds (CdI{sub 2} type) with a large inter-sheet distance, and on 3-D spinel models with a huge number of vacant sites. The method is based on a correlation between experimental studies (XAFS, DX, Moessbauer, XPS) and theoretical calculations and on the electronic and electrochemical characteristics. The model proposed should allow to improve materials in a predictive way (type of substitution) or to imagine new materials. (J.S.) 15 refs.

Influence of composition on phase occurrence during charge process of AB5+x Ni-MH negative electrode materials

International Nuclear Information System (INIS)

Vivet, S.; Latroche, M.; Chabre, Y.; Joubert, J.-M.; Knosp, B.; Percheron-Guegan, A.

2005-01-01

Multi-substituted LaNi 5 -type alloys (AB 5+ x ) are widely used as negative electrode materials in commercial Ni-MH batteries. Cobalt substitution on Ni sites allows to enhance battery cycle life by reducing alloy pulverization induced by hydrogen cycling. This improvement is attributed to the occurrence of a three-phase process (α, β and γ) during electrochemical hydrogen loading. In order to better understand the effect of the composition on the phase occurrence and to reduce the rate of costly cobalt, an in situ neutron diffraction study has been performed at room temperature during electrochemical charge of two different electrode materials MmNi 4.07 Mn 0.63 Al 0.2 M 0.4 with M=Fe and Mn and B/A=5.3. These cobalt free compounds show cycle life comparable to that of commercial materials. The results show that three phases are also observed for these samples. The γ-phase content depends on M and is higher for M=Fe than for M=Mn. These results are related to the improved cycle lives and to the alloy pulverization process

Stimulation and recording electrodes for neural prostheses

CERN Document Server

Pour Aryan, Naser; Rothermel, Albrecht

2015-01-01

This book provides readers with basic principles of the electrochemistry of the electrodes used in modern, implantable neural prostheses. The authors discuss the boundaries and conditions in which the electrodes continue to function properly for long time spans, which are required when designing neural stimulator devices for long-term in vivo applications. Two kinds of electrode materials, titanium nitride and iridium are discussed extensively, both qualitatively and quantitatively. The influence of the counter electrode on the safety margins and electrode lifetime in a two electrode system is explained. Electrode modeling is handled in a final chapter.

Insertion of Mono- vs. Bi- vs. Trivalent Atoms in Prospective Active Electrode Materials for Electrochemical Batteries: An ab Initio Perspective

Directory of Open Access Journals (Sweden)

Vadym V. Kulish

2017-12-01

Full Text Available Rational design of active electrode materials is important for the development of advanced lithium and post-lithium batteries. Ab initio modeling can provide mechanistic understanding of the performance of prospective materials and guide design. We review our recent comparative ab initio studies of lithium, sodium, potassium, magnesium, and aluminum interactions with different phases of several actively experimentally studied electrode materials, including monoelemental materials carbon, silicon, tin, and germanium, oxides TiO2 and VxOy as well as sulphur-based spinels MS2 (M = transition metal. These studies are unique in that they provided reliable comparisons, i.e., at the same level of theory and using the same computational parameters, among different materials and among Li, Na, K, Mg, and Al. Specifically, insertion energetics (related to the electrode voltage and diffusion barriers (related to rate capability, as well as phononic effects, are compared. These studies facilitate identification of phases most suitable as anode or cathode for different types of batteries. We highlight the possibility of increasing the voltage, or enabling electrochemical activity, by amorphization and p-doping, of rational choice of phases of oxides to maximize the insertion potential of Li, Na, K, Mg, Al, as well as of rational choice of the optimum sulfur-based spinel for Mg and Al insertion, based on ab initio calculations. Some methodological issues are also addressed, including construction of effective localized basis sets, applications of Hubbard correction, generation of amorphous structures, and the use of a posteriori dispersion corrections.

Li4 Ti5 O12 Anode: Structural Design from Material to Electrode and the Construction of Energy Storage Devices.

Science.gov (United States)

Chen, Zhijie; Li, Honsen; Wu, Langyuan; Lu, Xiaoxia; Zhang, Xiaogang

2018-03-01

Spinel Li 4 Ti 5 O 12 , known as a zero-strain material, is capable to be a competent anode material for promising applications in state-of-art electrochemical energy storage devices (EESDs). Compared with commercial graphite, spinel Li 4 Ti 5 O 12 offers a high operating potential of ∼1.55 V vs Li/Li + , negligible volume expansion during Li + intercalation process and excellent thermal stability, leading to high safety and favorable cyclability. Despite the merits of Li 4 Ti 5 O 12 been presented, there still remains the issue of Li 4 Ti 5 O 12 suffering from poor electronic conductivity, manifesting disadvantageous rate performance. Typically, a material modification process of Li 4 Ti 5 O 12 will be proposed to overcome such an issue. However, the previous reports have made few investigations and achievements to analyze the subsequent processes after a material modification process. In this review, we attempt to put considerable interest in complete device design and assembly process with its material structure design (or modification process), electrode structure design and device construction design. Moreover, we have systematically concluded a series of representative design schemes, which can be divided into three major categories involving: (1) nanostructures design, conductive material coating process and doping process on material level; (2) self-supporting or flexible electrode structure design on electrode level; (3) rational assembling of lithium ion full cell or lithium ion capacitor on device level. We believe that these rational designs can give an advanced performance for Li 4 Ti 5 O 12 -based energy storage device and deliver a deep inspiration. © 2018 The Chemical Society of Japan & Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Few-layered MoSe2 nanosheets as an advanced electrode material for supercapacitors.

Science.gov (United States)

Balasingam, Suresh Kannan; Lee, Jae Sung; Jun, Yongseok

2015-09-21

We report the synthesis of few-layered MoSe2 nanosheets using a facile hydrothermal method and their electrochemical charge storage behavior. A systematic study of the structure and morphology of the as-synthesized MoSe2 nanosheets was performed. The downward peak shift in the Raman spectrum and the high-resolution transmission electron microscopy images confirmed the formation of few-layered nanosheets. The electrochemical energy-storage behavior of MoSe2 nanosheets was also investigated for supercapacitor applications in a symmetric cell configuration. The MoSe2 nanosheet electrode exhibited a maximum specific capacitance of 198.9 F g(-1) and the symmetric device showed 49.7 F g(-1) at a scan rate of 2 mV s(-1). A capacitance retention of approximately 75% was observed even after 10 000 cycles at a high charge-discharge current density of 5 A g(-1). The two-dimensional MoSe2 nanosheets exhibited a high specific capacitance and good cyclic stability, which makes it a promising electrode material for supercapacitor applications.

International regulatory control of the transport of radioactive materials

International Nuclear Information System (INIS)

Swindell, G.E.

1979-01-01

The development of the IAEA regulations on the transport of radioactive materials and the background for the adoption of these regulations by the various international organizations responsible for regulating the different modes of international transport of hazardous materials is briefly discussed

High Speed, Low Cost Fabrication of Gas Diffusion Electrodes for Membrane Electrode Assemblies

Energy Technology Data Exchange (ETDEWEB)

DeCastro, Emory S.; Tsou, Yu-Min; Liu, Zhenyu

2013-09-20

Fabrication of membrane electrode assemblies (MEAs) depends on creating inks or pastes of catalyst and binder, and applying this suspension to either the membrane (catalyst coated membrane) or gas diffusion media (gas diffusion electrode) and respectively laminating either gas diffusion media or gas diffusion electrodes (GDEs) to the membrane. One barrier to cost effective fabrication for either of these approaches is the development of stable and consistent suspensions. This program investigated the fundamental forces that destabilize the suspensions and developed innovative approaches to create new, highly stable formulations. These more concentrated formulations needed fewer application passes, could be coated over longer and wider substrates, and resulted in significantly lower coating defects. In March of 2012 BASF Fuel Cell released a new high temperature product based on these advances, whereby our customers received higher performing, more uniform MEAs resulting in higher stack build yields. Furthermore, these new materials resulted in an “instant” increase in capacity due to higher product yields and material throughput. Although not part of the original scope of this program, these new formulations have also led us to materials that demonstrate equivalent performance with 30% less precious metal in the anode. This program has achieved two key milestones in DOE’s Manufacturing R&D program: demonstration of processes for direct coating of electrodes and continuous in-line measurement for component fabrication.

Internal reflection flash photolysis study of the photochemistry of eosin at TiO sub 2 semiconductor electrodes

Energy Technology Data Exchange (ETDEWEB)

Ryan, M.A.; Fitzgerald, E.C.; Spitler, M.T. (Polaroid Corp., Cambridge, MA (USA))

1989-08-10

It is shown that the photoelectrochemical data on eosin Y sensitized TiO{sub 2} single-crystal electrodes cannot be interpreted unambiguously without concomitant data from flash photolysis measurements on this system. By use of a combination of internal reflection spectroscopy and laser flash photolysis, electron exchange with TiO{sub 2} was observed for the excited singlet state, the triplet state, and the cation radical of the dye. With a temporal resolution of 100 ns, the kinetics of the charge transfer are compared with those of the dye in solution and used to interpret the photoelectrochemistry of the dye at the electrode. Spectroscopic evidence revealed photocurrent production by the triplet state and a reduction of the eosin cation radical by electrons from the TiO{sub 2} conduction band and by hydroquinone.

Original Conductive Nano-Co3O4 Investigated as Electrode Material for Hybrid Supercapacitors

OpenAIRE

Godillot, Gérôme; Guerlou-Demourgues, Liliane; Taberna, Pierre-Louis; Simon, Patrice; Delmas, Claude

2011-01-01

Cobalt oxides have been extensively used as conductive additives for Ni-MH batteries. We report in this paper the performances of an original nanometric cobalt oxide, close to Co3O4, as electrode material for hybrid supercapacitors. This spinel type phase contains hydrogen, lithium, cobalt vacancies, and especially Co4þ ions within the structure, leading to a high electronic conductivity. Cyclic voltammetry and impedance spectroscopy measurements show interesting capacitance (320 F/g in 8M-KO...

Redox electrodes comprised of polymer-modified carbon nanomaterials

Science.gov (United States)

Roberts, Mark; Emmett, Robert; Karakaya, Mehmet; Podila, Ramakrishna; Rao, Apparao; Clemson Physics Team; Clemson Chemical Engineering Team

2013-03-01

A shift in how we generate and use electricity requires new energy storage materials and systems compatible with hybrid electric transportation and the integration of renewable energy sources. Supercapacitors provide a solution to these needs by combining the high power, rapid switching, and exceptional cycle life of a capacitor with the high energy density of a battery. Our research brings together nanotechnology and materials chemistry to address the limitations of electrode materials. Paper electrodes fabricated with various forms of carbon nanomaterials, such as nanotubes, are modified with redox-polymers to increase the electrode's energy density while maintaining rapid discharge rates. In these systems, the carbon nanomaterials provide the high surface area, electrical conductivity, nanoscale and porosity, while the redox polymers provide a mechanism for charge storage through Faradaic charge transfer. The design of redox polymers and their incorporation into nanomaterial electrodes will be discussed with a focus on enabling high power and high energy density electrodes.

Removal of suspended solids and turbidity from marble processing wastewaters by electrocoagulation: Comparison of electrode materials and electrode connection systems

Energy Technology Data Exchange (ETDEWEB)

Solak, Murat [Duezce University, Kaynasli Vocational School, Environmental Protection and Control Department, 81900 Duezce (Turkey); Kilic, Mehmet, E-mail: kavi@mmf.sdu.edu.tr [Sueleyman Demirel University, Engineering and Architecture Faculty, Environmental Engineering Department, 32260 Isparta (Turkey); Hueseyin, Yazici; Sencan, Aziz [Sueleyman Demirel University, Engineering and Architecture Faculty, Environmental Engineering Department, 32260 Isparta (Turkey)

2009-12-15

In this study, removal of suspended solids (SS) and turbidity from marble processing wastewaters by electrocoagulation (EC) process were investigated by using aluminium (Al) and iron (Fe) electrodes which were run in serial and parallel connection systems. To remove these pollutants from the marble processing wastewater, an EC reactor including monopolar electrodes (Al/Fe) in parallel and serial connection system, was utilized. Optimization of differential operation parameters such as pH, current density, and electrolysis time on SS and turbidity removal were determined in this way. EC process with monopolar Al electrodes in parallel and serial connections carried out at the optimum conditions where the pH value was 9, current density was approximately 15 A/m{sup 2}, and electrolysis time was 2 min resulted in 100% SS removal. Removal efficiencies of EC process for SS with monopolar Fe electrodes in parallel and serial connection were found to be 99.86% and 99.94%, respectively. Optimum parameters for monopolar Fe electrodes in both of the connection types were found to be for pH value as 8, for electrolysis time as 2 min. The optimum current density value for Fe electrodes used in serial and parallel connections was also obtained at 10 and 20 A/m{sup 2}, respectively. Based on the results obtained, it was found that EC process running with each type of the electrodes and the connections was highly effective for the removal of SS and turbidity from marble processing wastewaters, and that operating costs with monopolar Al electrodes in parallel connection were the cheapest than that of the serial connection and all the configurations for Fe electrode.

Removal of suspended solids and turbidity from marble processing wastewaters by electrocoagulation: Comparison of electrode materials and electrode connection systems

International Nuclear Information System (INIS)

Solak, Murat; Kilic, Mehmet; Hueseyin, Yazici; Sencan, Aziz

2009-01-01

In this study, removal of suspended solids (SS) and turbidity from marble processing wastewaters by electrocoagulation (EC) process were investigated by using aluminium (Al) and iron (Fe) electrodes which were run in serial and parallel connection systems. To remove these pollutants from the marble processing wastewater, an EC reactor including monopolar electrodes (Al/Fe) in parallel and serial connection system, was utilized. Optimization of differential operation parameters such as pH, current density, and electrolysis time on SS and turbidity removal were determined in this way. EC process with monopolar Al electrodes in parallel and serial connections carried out at the optimum conditions where the pH value was 9, current density was approximately 15 A/m 2 , and electrolysis time was 2 min resulted in 100% SS removal. Removal efficiencies of EC process for SS with monopolar Fe electrodes in parallel and serial connection were found to be 99.86% and 99.94%, respectively. Optimum parameters for monopolar Fe electrodes in both of the connection types were found to be for pH value as 8, for electrolysis time as 2 min. The optimum current density value for Fe electrodes used in serial and parallel connections was also obtained at 10 and 20 A/m 2 , respectively. Based on the results obtained, it was found that EC process running with each type of the electrodes and the connections was highly effective for the removal of SS and turbidity from marble processing wastewaters, and that operating costs with monopolar Al electrodes in parallel connection were the cheapest than that of the serial connection and all the configurations for Fe electrode.

Removal of suspended solids and turbidity from marble processing wastewaters by electrocoagulation: comparison of electrode materials and electrode connection systems.

Science.gov (United States)

Solak, Murat; Kiliç, Mehmet; Hüseyin, Yazici; Sencan, Aziz

2009-12-15

In this study, removal of suspended solids (SS) and turbidity from marble processing wastewaters by electrocoagulation (EC) process were investigated by using aluminium (Al) and iron (Fe) electrodes which were run in serial and parallel connection systems. To remove these pollutants from the marble processing wastewater, an EC reactor including monopolar electrodes (Al/Fe) in parallel and serial connection system, was utilized. Optimization of differential operation parameters such as pH, current density, and electrolysis time on SS and turbidity removal were determined in this way. EC process with monopolar Al electrodes in parallel and serial connections carried out at the optimum conditions where the pH value was 9, current density was approximately 15 A/m(2), and electrolysis time was 2 min resulted in 100% SS removal. Removal efficiencies of EC process for SS with monopolar Fe electrodes in parallel and serial connection were found to be 99.86% and 99.94%, respectively. Optimum parameters for monopolar Fe electrodes in both of the connection types were found to be for pH value as 8, for electrolysis time as 2 min. The optimum current density value for Fe electrodes used in serial and parallel connections was also obtained at 10 and 20 A/m(2), respectively. Based on the results obtained, it was found that EC process running with each type of the electrodes and the connections was highly effective for the removal of SS and turbidity from marble processing wastewaters, and that operating costs with monopolar Al electrodes in parallel connection were the cheapest than that of the serial connection and all the configurations for Fe electrode.

Introduction to reactor internal materials for pressurized water reactor

Energy Technology Data Exchange (ETDEWEB)

Ryu, Woo Suk; Hong, Joon Hwa; Jee, Se Hwan; Lee, Bong Sang; Kuk, Il Hyun [Korea Atomic Energy Research Institute, Taejon (Korea, Republic of)

1994-06-01

This report reviewed the R and D states of reactor internal materials in order to be a reference for researches and engineers who are concerning on localization of the materials in the field or laboratory. General structure of PWR internals and material specification for YGN 3 and 4 were reviewed. States-of-arts on R and D of stainless steel and Alloy X-750 were reviewed, and degradation mechanisms of the components were analyzed. In order to develop the good domestic materials for reactor internal, following studies would be carried out: microstructure, sensitization behavior, fatigue property, irradiation-induced stress corrosion cracking/radiation-induced segregation, radiation embrittlement. (Author) 7 refs., 14 figs., 5 tabs.,.

Introduction to reactor internal materials for pressurized water reactor

International Nuclear Information System (INIS)

Ryu, Woo Suk; Hong, Joon Hwa; Jee, Se Hwan; Lee, Bong Sang; Kuk, Il Hyun

1994-06-01

This report reviewed the R and D states of reactor internal materials in order to be a reference for researches and engineers who are concerning on localization of the materials in the field or laboratory. General structure of PWR internals and material specification for YGN 3 and 4 were reviewed. States-of-arts on R and D of stainless steel and Alloy X-750 were reviewed, and degradation mechanisms of the components were analyzed. In order to develop the good domestic materials for reactor internal, following studies would be carried out: microstructure, sensitization behavior, fatigue property, irradiation-induced stress corrosion cracking/radiation-induced segregation, radiation embrittlement. (Author) 7 refs., 14 figs., 5 tabs.,

Internal Morphologies of Cycled Li-Metal Electrodes Investigated by Nano-Scale Resolution X-ray Computed Tomography.

Science.gov (United States)

Frisco, Sarah; Liu, Danny X; Kumar, Arjun; Whitacre, Jay F; Love, Corey T; Swider-Lyons, Karen E; Litster, Shawn

2017-06-07

While some commercially available primary batteries have lithium metal anodes, there has yet to be a commercially viable secondary battery with this type of electrode. Research prototypes of these cells typically exhibit a limited cycle life before dendrites form and cause internal cell shorting, an occurrence that is more pronounced during high-rate cycling. To better understand the effects of high-rate cycling that can lead to cell failure, we use ex situ nanoscale-resolution X-ray computed tomography (nano-CT) with the aid of Zernike phase contrast to image the internal morphologies of lithium metal electrodes on copper wire current collectors that have been cycled at low and high current densities. The Li that is deposited on a Cu wire and then stripped and deposited at low current density appears uniform in morphology. Those cycled at high current density undergo short voltage transients to >3 V during Li-stripping from the electrode, during which electrolyte oxidation and Cu dissolution from the current collector may occur. The effect of temperature is also explored with separate cycling experiments performed at 5 and 33 °C. The resulting morphologies are nonuniform films filled with voids that are semispherical in shape with diameters ranging from hundreds of nanometers to tens of micrometers, where the void size distributions are temperature-dependent. Low-temperature cycling elicits a high proportion of submicrometer voids, while the higher-temperature sample morphology is dominated by voids larger than 2 μm. In evaluating these morphologies, we consider the importance of nonidealities during extreme charging, such as electrolyte decomposition. We conclude that nano-CT is an effective tool for resolving features and aggressive cycling-induced anomalies in Li films in the range of 100 nm to 100 μm.

Three-dimensional Hierarchical Metal oxide-Carbon Electrode Material for High Efficient Microbial Electrosynthesis

DEFF Research Database (Denmark)

Cui, Mengmeng; Nie, Huarong; Zhang, Tian

2017-01-01

pore structure in a microwave oven is demonstrated. Microwave pyrolysis of ferrocene using carbon felt as a microwave absorber, a method that is rapid (tens of seconds), does not require harsh conditions nor costly equipment is utilized, and can be readily scaled up. The produced material has a high...... specific surface area, a multi-length scale porous structure and a high conductivity, and is quite stable, making it promising for many practical applications. As an electrode in microbial electrosynthesis, the performance is improved by a factor of five and an optimal biofilm of the microorganism...

Hybrid nanomaterial of α-Co(OH)2 nanosheets and few-layer graphene as an enhanced electrode material for supercapacitors.

Science.gov (United States)

Cheng, J P; Liu, L; Ma, K Y; Wang, X; Li, Q Q; Wu, J S; Liu, F

2017-01-15

Supercapacitor with metal hydroxide nanosheets as electrode can have high capacitance. However, the cycling stability and high rate capacity is low due to the low electrical conductivity. Here, the exfoliated α-Co(OH) 2 nanosheets with high capacitance has been assembled on few-layer graphene with high electric conductivity by a facile yet effective and scalable solution method. Exfoliated hydrotalcite-like α-Co(OH) 2 nanosheets and few-layer graphene suspensions were prepared by a simple ultrasonication in formamide and N-methyl-2-pyrrolidone, respectively. Subsequently, a hybrid was made by self-assembly of α-Co(OH) 2 and few-layer graphene when the two dispersions were mixed at room temperature. The hybrid material provided a high specific capacitance of 567.1F/g at 1A/g, while a better rate capability and better stability were achieved compared to that mad of pristine and single exfoliated α-Co(OH) 2 . When the hybrid nanocomposite was used as a positive electrode and activated carbon was applied as negative electrode to assembly an asymmetric capacitor, an energy density of 21.2Wh/kg at a power density of 0.41kW/kg within a potential of 1.65V was delivered. The high electrochemical performance and facile solution-based synthesis method suggested that the hybrid of exfoliated α-Co(OH) 2 /few-layer graphene could be a potential electrode material for electrochemical capacitor. Copyright © 2016 Elsevier Inc. All rights reserved.

Enhanced power generation in annular single-chamber microbial fuel cell via optimization of electrode spacing using chocolate industry wastewater.

Science.gov (United States)

Noori, Parisa; Najafpour Darzi, Ghasem

2016-05-01

Development and practical application of microbial fuel cell (MFC) is restricted because of the limitations such as low power output. To overcome low power limitation, the optimization of specific parameters including electrode materials and surface area, electrode spacing, and MFC's cell shape was investigated. To the best of our knowledge, no investigation has been reported in the literature to implement an annular single-chamber microbial fuel cell (ASCMFC) using chocolate industry wastewater. ASCMFC was fabricated via optimization of the stated parameters. The aspects of ASCMFC were comprehensively examined. In this study, the optimization of electrode spacing and its impact on performance of the ASCMFC were conducted. Reduction of electrode spacing by 46.15% (1.3-0.7 cm) resulted in a decrease in internal resistance from 100 to 50 Ω, which enhanced the power density and current output to 22.898 W/m(3) and 6.42 mA, respectively. An optimum electrode spacing of 0.7 cm was determined. Through this paper, the effects of these parameters and the performance of ASCMFC are also evaluated. © 2015 International Union of Biochemistry and Molecular Biology, Inc.

Organic photosensitive cells grown on rough electrode with nano-scale morphology control

Science.gov (United States)

Yang, Fan [Piscataway, NJ; Forrest, Stephen R [Ann Arbor, MI

2011-06-07

An optoelectronic device and a method for fabricating the optoelectronic device includes a first electrode disposed on a substrate, an exposed surface of the first electrode having a root mean square roughness of at least 30 nm and a height variation of at least 200 nm, the first electrode being transparent. A conformal layer of a first organic semiconductor material is deposited onto the first electrode by organic vapor phase deposition, the first organic semiconductor material being a small molecule material. A layer of a second organic semiconductor material is deposited over the conformal layer. At least some of the layer of the second organic semiconductor material directly contacts the conformal layer. A second electrode is deposited over the layer of the second organic semiconductor material. The first organic semiconductor material is of a donor-type or an acceptor-type relative to the second organic semiconductor material, which is of the other material type.

Composite carbon foam electrode

Science.gov (United States)

Mayer, Steven T.; Pekala, Richard W.; Kaschmitter, James L.

1997-01-01

Carbon aerogels used as a binder for granularized materials, including other forms of carbon and metal additives, are cast onto carbon or metal fiber substrates to form composite carbon thin film sheets. The thin film sheets are utilized in electrochemical energy storage applications, such as electrochemical double layer capacitors (aerocapacitors), lithium based battery insertion electrodes, fuel cell electrodes, and electrocapacitive deionization electrodes. The composite carbon foam may be formed by prior known processes, but with the solid particles being added during the liquid phase of the process, i.e. prior to gelation. The other forms of carbon may include carbon microspheres, carbon powder, carbon aerogel powder or particles, graphite carbons. Metal and/or carbon fibers may be added for increased conductivity. The choice of materials and fibers will depend on the electrolyte used and the relative trade off of system resistivty and power to system energy.

Drop detachment and motion on fuel cell electrode materials.

Science.gov (United States)

Gauthier, Eric; Hellstern, Thomas; Kevrekidis, Ioannis G; Benziger, Jay

2012-02-01

Liquid water is pushed through flow channels of fuel cells, where one surface is a porous carbon electrode made up of carbon fibers. Water drops grow on the fibrous carbon surface in the gas flow channel. The drops adhere to the superficial fiber surfaces but exhibit little penetration into the voids between the fibers. The fibrous surfaces are hydrophobic, but there is a substantial threshold force necessary to initiate water drop motion. Once the water drops begin to move, however, the adhesive force decreases and drops move with minimal friction, similar to motion on superhydrophobic materials. We report here studies of water wetting and water drop motion on typical porous carbon materials (carbon paper and carbon cloth) employed in fuel cells. The static coefficient of friction on these textured surfaces is comparable to that for smooth Teflon. But the dynamic coefficient of friction is several orders of magnitude smaller on the textured surfaces than on smooth Teflon. Carbon cloth displays a much smaller static contact angle hysteresis than carbon paper due to its two-scale roughness. The dynamic contact angle hysteresis for carbon paper is greatly reduced compared to the static contact angle hysteresis. Enhanced dynamic hydrophobicity is suggested to result from the extent to which a dynamic contact line can track topological heterogeneities of the liquid/solid interface.

Evaluation of excess nuclear materials suitability for international safeguards

International Nuclear Information System (INIS)

Newton, J.W.; White, W.C.; Davis, R.M.; Cherry, R.C.

1996-01-01

President Clinton announced in March 1995 the permanent withdrawal of 200 tons of fissile material from the US nuclear stockpile. This action was made possible by the dramatic reduction in nuclear weapons stockpile size and a desire to demonstrate the US'' commitment to nonproliferation goals. To provide further assurance of that commitment, the US is addressing placement of these materials under International Atomic Energy Agency (IAEA) safeguards. An initial step of this overall assessment was evaluation of the nuclear materials'' suitability for international safeguards. US Department of Energy (DOE) field organizations reviewed a detailed listing of all candidate materials with respect to characterization status, security classification, and acceptability for international safeguards compared to specified criteria. These criteria included form, location, environment and safety considerations, measurability, and stability. The evaluation resulted in broad categorizations of all materials with respect to preparing and placing materials under IAEA safeguards and provided essential information for decisions on the timing for offering materials as a function of materials attributes. A plan is being prepared to determine the availability of these materials for IAEA safeguards considering important factors such as costs, processes and facilities required to prepare materials, and impacts on other programs

Long Life Nickel Electrodes for Nickel-Hydrogen Cells: Fiber Substrates Nickel Electrodes

Science.gov (United States)

Rogers, Howard H.

2000-01-01

Samples of nickel fiber mat electrodes were investigated over a wide range of fiber diameters, electrode thickness, porosity and active material loading levels. Thickness' were 0.040, 0.060 and 0.080 inches for the plaque: fiber diameters were primarily 2, 4, and 8 micron and porosity was 85, 90, and 95%. Capacities of 3.5 in. diameter electrodes were determined in the flooded condition with both 26 and 31% potassium hydroxide solution. These capacity tests indicated that the highest capacities per unit weight were obtained at the 90% porosity level with a 4 micron diameter fiber plaque. It appeared that the thinner electrodes had somewhat better performance, consistent with sintered electrode history. Limited testing with two-positive-electrode boiler plate cells was also carried out. Considerable difficulty with constructing the cells was encountered with short circuits the major problem. Nevertheless, four cells were tested. The cell with 95% porosity electrodes failed during conditioning cycling due to high voltage during charge. Discharge showed that this cell had lost nearly all of its capacity. The other three cells after 20 conditioning cycles showed capacities consistent with the flooded capacities of the electrodes. Positive electrodes made from fiber substrates may well show a weight advantage of standard sintered electrodes, but need considerably more work to prove this statement. A major problem to be investigated is the lower strength of the substrate compared to standard sintered electrodes. Problems with welding of leads were significant and implications that the electrodes would expand more than sintered electrodes need to be investigated. Loading levels were lower than had been expected based on sintered electrode experiences and the lower loading led to lower capacity values. However, lower loading causes less expansion and contraction during cycling so that stress on the substrate is reduced.

Poly(ethylene terephthalate)-based carbons as electrode material in supercapacitors

Energy Technology Data Exchange (ETDEWEB)

Domingo-Garcia, M.; Almazan-Almazan, M.C.; Lopez-Garzon, F.J. [Dpto de Quimica Inorganica, Facultad de Ciencias, 18071 Granada (Spain); Fernandez, J.A.; Centeno, T.A. [Instituto Nacional del Carbon-CSIC, Apartado 73, 33080 Oviedo (Spain); Stoeckli, F. [Physics Department, University of Neuchatel, Rue Emile Argand 11, CH-2009 Neuchatel (Switzerland)

2010-06-15

A systematic study by complementary techniques shows that PET-waste from plastic vessels is a competitive precursor of carbon electrodes for supercapacitors. PET derived-activated carbons follow the general trends observed for highly porous carbons and display specific capacitances at low current density as high as 197 F g{sup -1} in 2 M H{sub 2}SO{sub 4} aqueous electrolyte and 98 F g{sup -1} in the aprotic medium 1 M (C{sub 2}H{sub 5}){sub 4}NBF{sub 4}/acetonitrile. Additionally, high performance has also been achieved at high current densities, which confirms the potential of this type of materials for electrical energy storage. A new method based on the basic solvolysis of PET-waste and the subsequent carbonization seems to be an interesting alternative to obtain porous carbons with enhanced properties for supercapacitors. (author)

Magnetohydrodynamic electrode

International Nuclear Information System (INIS)

1980-01-01

The object of the invention is the provision of a material capable of withstanding a high-temperature, corrosive and erosive environment for use as a ceramic-metal composite electrode current collector in the channel of a magnetohydrodynamic generator. (U.K.)

International nuclear safety center database on material properties

International Nuclear Information System (INIS)

Fink, J.K.

1996-01-01

International nuclear safety center database on the following material properties is described: fuel, cladding,absorbers, moderators, structural materials, coolants, concretes, liquid mixtures, uranium dioxide

Methods for and products of processing nanostructure nitride, carbonitride and oxycarbonitride electrode power materials by utilizing sol gel technology for supercapacitor applications

Science.gov (United States)

Huang, Yuhong; Wei, Oiang; Chu, Chung-tse; Zheng, Haixing

2001-01-01

Metal nitride, carbonitride, and oxycarbonitride powder with high surface area (up to 150 m.sup.2 /g) is prepared by using sol-gel process. The metal organic precursor, alkoxides or amides, is synthesized firstly. The metal organic precursor is modified by using unhydrolyzable organic ligands or templates. A wet gel is formed then by hydrolysis and condensation process. The solvent in the wet gel is then be removed supercritically to form porous amorphous hydroxide. This porous hydroxide materials is sintered to 725.degree. C. under the ammonia flow and porous nitride powder is formed. The other way to obtain high surface area nitride, carbonitride, and oxycarbonitride powder is to pyrolyze polymerized templated metal amides aerogel in an inert atmosphere. The electrochemical capacitors are prepared by using sol-gel prepared nitride, carbonitride, and oxycarbonitride powder. Two methods are used to assemble the capacitors. Electrode is formed either by pressing the mixture of nitride powder and binder to a foil, or by depositing electrode coating onto metal current collector. The binder or coating is converted into a continuous network of electrode material after thermal treatment to provide enhanced energy and power density. Liquid electrolyte is soaked into porous electrode. The electrochemical capacitor assembly further has a porous separator layer between two electrodes/electrolyte and forming a unit cell.

Polyaniline-Manganese dioxide nanorods nanocomposite as an electrode material for supercapacitors

Science.gov (United States)

Ahirrao, Dinesh J.; Jha, Neetu

2017-05-01

Supercapacitors (SC) are energy storage devices with long durability, and high power density. Metal oxides, conducting polymers and carbon based nanomaterials are generally used as an electrode material in SC due to their high charge storage properties. Superior performance of SC can be achieved by making a composite of metal oxides with conducting polymer or with carbon based nanomaterials in order achieve synergy. Herein, we report a low temperature hydrothermal method for the synthesis of α-MnO2 nanorods (α-MnO2-NR) and the composite was prepared by in situ polymerization of polyaniline (PANT) with α-MnO2-NR. Uniform distribution of MnO2-NR on the PANI granules was observed in composite. Material characterization was carried out by using XRD, FTIR and scanning electron microscopy (SEM). Electrochemical performance of the as-prepared materials was evaluated by using cyclic voltammetry (CV) and galvanostatic charge-discharge (GCD) measurements in potential range of 0 to 0.8 V. PANI-α-MnO2-NR showed improved specific capacitance of 605 F/g at 1 A/g which is higher than that of individual component like pure PANI (515 F/g) and pure MnO2-NR (141 F/g) at 1A/g.

3D nitrogen-doped graphene aerogel nanomesh: Facile synthesis and electrochemical properties as the electrode materials for supercapacitors

Science.gov (United States)

Su, Xiao-Li; Fu, Lin; Cheng, Ming-Yu; Yang, Jing-He; Guan, Xin-Xin; Zheng, Xiu-Cheng

2017-12-01

Nitrogen-doped graphene aerogel nanomesh (N-GANM) has been hydrothermally prepared from graphene oxide and ammonium hydroxide using iron nitrate as the etching agent. The results showed that N-GANM with an interesting nanomesh structure on the graphene sheets maintained the 3D architecture of graphene aerogel (GA). Furthermore, it exhibited excellent electrochemical capacitive behavior and the specific capacitance value (290.0 F g-1 at 1 A g-1) remained approximately 90.3% after 2000 cycles in the three-electrode system. In addition, N-GANM displayed an energy density of 30.9 Wh kg-1 at the power density of 450.3 W kg-1 and excellent cycling stability retention (98%) after 10,000 cycles in the two-electrode symmetric device. The resulting N-GANM was expected to be a much favorable supercapacitor electrode material due to the heteroatom-doping and its unique porous structure.

Effects of crystalline quality and electrode material on fatigue in Pb(Zr,Ti)O3 thin film capacitors

Science.gov (United States)

Lee, J.; Johnson, L.; Safari, A.; Ramesh, R.; Sands, T.; Gilchrist, H.; Keramidas, V. G.

1993-07-01

Pb(Zr(0.52)Ti(0.48))O3 (PZT)/Y1Ba2Cu3O(x) (YBCO) heterostructures were grown by pulsed laser deposition, in which PZT films were epitaxial, highly oriented, or polycrystalline. These PZT films were obtained by varying the deposition temperature from 550 to 760 C or by using various substrates such as SrTiO3 (100), MgO (100), and r-plane sapphire. PZT films with Pt top electrodes exhibited large fatigue with 35-50 percent loss of the remanent polarization after 10 exp 9 cycles, depending on the crystalline quality. Polycrystalline films showed better fatigue resistance than epitaxial or highly oriented films. However, PZT films with both top and bottom YBCO electrodes had significantly improved fatigue resistance for both epitaxial and polycrystalline films. Electrode material seems to be a more important parameter in fatigue than the crystalline quality of the PZT films.

Layered assembly of graphene oxide and Co-Al layered double hydroxide nanosheets as electrode materials for supercapacitors.

Science.gov (United States)

Wang, Lei; Wang, Dong; Dong, Xin Yi; Zhang, Zhi Jun; Pei, Xian Feng; Chen, Xin Jiang; Chen, Biao; Jin, Jian

2011-03-28

An innovative strategy of fabricating electrode material by layered assembling two kinds of one-atom-thick sheets, carboxylated graphene oxide (GO) and Co-Al layered double hydroxide nanosheet (Co-Al LDH-NS) for the application as a pseudocapacitor is reported. The Co-Al LDH-NS/GO composite exhibits good energy storage properties.

Graphene oxide-mediated electrochemistry of glucose oxidase on glassy carbon electrodes.

Science.gov (United States)

Castrignanò, Silvia; Valetti, Francesca; Gilardi, Gianfranco; Sadeghi, Sheila J

2016-01-01

Glucose oxidase (GOD) was immobilized on glassy carbon electrodes in the presence of graphene oxide (GO) as a model system for the interaction between GO and biological molecules. Lyotropic properties of didodecyldimethylammonium bromide (DDAB) were used to stabilize the enzymatic layer on the electrode surface resulting in a markedly improved electrochemical response of the immobilized GOD. Transmission electron microscopy images of the GO with DDAB confirmed the distribution of the GO in a two-dimensional manner as a foil-like material. Although it is known that glassy carbon surfaces are not ideal for hydrogen peroxide detection, successful chronoamperometric titrations of the GOD in the presence of GO with β-d-glucose were performed on glassy carbon electrodes, whereas no current response was detected upon β-d-glucose addition in the absence of GO. The GOD-DDAB-GO system displayed a high turnover efficiency and substrate affinity as a glucose biosensor. The simplicity and ease of the electrode preparation procedure of this GO/DDAB system make it a good candidate for immobilizing other biomolecules for fabrication of amperometric biosensors. © 2015 International Union of Biochemistry and Molecular Biology, Inc.

Nanoporous carbon derived from agro-waste pineapple leaves for supercapacitor electrode

Science.gov (United States)

Sodtipinta, Jedsada; Amornsakchai, Taweechai; Pakawatpanurut, Pasit

2017-09-01

By using KOH as the chemical activating agent in the synthesis, the activated carbon derived from pineapple leaf fiber (PALF) was prepared. The structure, morphology, and the surface functional groups of the as-prepared activated carbon were investigated using x-ray diffraction, field emission scanning electron microscope equipped with energy dispersive x-ray spectroscopy, and x-ray photoelectron spectroscopy. The electrochemical behavior and performance of the as-synthesized activated carbon electrode were measured using the cyclic voltammetry and the electrochemical impedance spectroscopy in 1 M Na2SO4 electrolyte solution in three-electrode setup. The activated carbon electrode exhibited the specific capacitance of 131.3 F g-1 at a scan rate of 5 mV s-1 with excellent cycling stability. The capacitance retention after 1000 cycles was about 97% of the initial capacitance at a scan rate of 30 mV s-1. Given these good electrochemical properties along with the high abundance of PALF, this activated carbon electrode has the potential to be one of the materials for future large-scale production of the electrochemical capacitors. Invited talk at 5th Thailand International Nanotechnology Conference (Nano Thailand-2016), 27-29 November 2016, Nakhon Ratchasima, Thailand.

Recent progress in hollow sphere-based electrodes for high-performance supercapacitors

Science.gov (United States)

Zhao, Yan; Chen, Min; Wu, Limin

2016-08-01

Hollow spheres have drawn much attention in the area of energy storage and conversion, especially in high-performance supercapacitors owing to their well-defined morphologies, uniform size, low density and large surface area. And quite some significant breakthroughs have been made in advanced supercapacitor electrode materials with hollow sphere structures. In this review, we summarize and discuss the synthesis and application of hollow spheres with controllable structure and morphology as electrode materials for supercapacitors. First, we briefly introduce the fabrication strategies of hollow spheres for electrode materials. Then, we discuss in detail the recent advances in various hollow sphere-based electrode materials for supercapacitors, including single-shelled, yolk-shelled, urchin-like, double-shelled, multi-shelled, and mesoporous hollow structure-based symmetric and asymmetric supercapacitor devices. We conclude this review with some perspectives on the future research and development of the hollow sphere-based electrode materials.

Recent progress in hollow sphere-based electrodes for high-performance supercapacitors.

Science.gov (United States)

Zhao, Yan; Chen, Min; Wu, Limin

2016-08-26

Hollow spheres have drawn much attention in the area of energy storage and conversion, especially in high-performance supercapacitors owing to their well-defined morphologies, uniform size, low density and large surface area. And quite some significant breakthroughs have been made in advanced supercapacitor electrode materials with hollow sphere structures. In this review, we summarize and discuss the synthesis and application of hollow spheres with controllable structure and morphology as electrode materials for supercapacitors. First, we briefly introduce the fabrication strategies of hollow spheres for electrode materials. Then, we discuss in detail the recent advances in various hollow sphere-based electrode materials for supercapacitors, including single-shelled, yolk-shelled, urchin-like, double-shelled, multi-shelled, and mesoporous hollow structure-based symmetric and asymmetric supercapacitor devices. We conclude this review with some perspectives on the future research and development of the hollow sphere-based electrode materials.

Electrode erosion in arc discharges at atmospheric pressure

Science.gov (United States)

Hardy, T. L.

1985-01-01

An experimental investigation was performed in an effort to measure and increase lifetime of electrodes in an arcjet thruster. The electrode erosion of various anode and cathode materials was measured after tests in an atmospheric pressure nitrogen arc discharge at powers less than 1 kW. A free-burning arc configuration and a constricted arc configuration were used to test the materials. Lanthanum hexboride and thoriated tungsten had low cathode erosion rates while thoriated tungsten and pure tungsten had the lowest anode erosion rates of the materials tested. Anode cooling, reverse gas flow, an external magnetic fields were all found to reduce electrode mass loss.

The regulations concerning the uses of international controlled material

International Nuclear Information System (INIS)

1978-01-01

These provisions are established on the basis of and to enforce ''The law for the regulations of nuclear source materials, nuclear fuel materials and reactors'' and the ''Prescriptions on the usage of internationally regulated goods'' in the Enforcement Ordinance of the Law. Terms are explained, such as area for incoming and outgoing of goods, main measuring point, batch and real stocks. Applications for the permission of the use of internationally regulated goods shall be filed, in which the kinds of such goods for the materials and equipments in each partner country, with which international agreement was concluded, and the quantity and expected period of use of each regulated material must be written. The users of such regulated materials shall keep the records on the usage of such materials in each factory or establishment. Such records include the quantities of receiving and delivering and stocks of nuclear raw material of each kind, radiation control reports and the records of accidents in the facilities for using nuclear raw materials. Applications for the approval of the stipulation on the management of measurement shall be filed, in which the functions and organizations of the persons engaging in the measurement and control of internationally regulated goods, the establishment of the areas for receiving and delivering the goods and the marks to be put on such areas, etc. Applications for the designation as the persons engaging in information processing works are specified. (Okada, K.)

Synthesis and characterization of natural dye and counter electrode thin films with different carbon materials for dye-sensitized solar cells.

Science.gov (United States)

Chang, Ho; Chen, Tien-Li; Kao, Mu-Jung; Chen, Chih-Hao; Chien, Shu-Hua; Jiang, Lii-Jenq

2011-08-01

This study aims to deal with the film of the counter electrode of dye-sensitized solar cells (DSSCs) and the preparation, structure and characteristics of the extract of natural dye. This study adopts different commercial carbon materials such as black lead, carbon black and self-made TiO2-MWCNT compound nanoparticle as the film of the counter electrodes. Moreover, for the preparation of natural dyes, anthocyanins and chlorophyll dyes are extracted from mulberry and pomegranate respectively. Furthermore, the extracted anthocyanins and chlorophyll are blended into cocktail dye to complete the preparation of natural dye. Results show that the photoelectric conversion efficiency of the single-layer TiO2-MWCNT counter electrode film and the cocktail dye of the DSSCs is 0.462%.

International conventions for measuring radioactivity of building materials

International Nuclear Information System (INIS)

Tan Chenglong

2004-01-01

In buildings, whether civil or industrial, natural radioactivity always occurs at different degrees in the materials (main building materials, decorative materials). Concerns on radioactivity from building materials is unavoidable for human living and developing. As a member of WTO, China's measuring method of radioactivity for building materials, including radionuclides limitation for building materials, hazard evaluation system etc, should keep accordance with the international rules and conventions. (author)

Sol-gel preparation of cobalt manganese mixed oxides for their use as electrode materials in lithium cells

International Nuclear Information System (INIS)

Lavela, P.; Tirado, J.L.; Vidal-Abarca, C.

2007-01-01

An ethanol dehydration procedure has been used to precipitate gel-like citrate precursors containing cobalt and manganese transition metal ions. Further annealing led to the Mn x Co 3-x O 4 spinel oxide series (x: 1, 1.5, 2, 3). Annealing temperature and treatment time were also evaluated to optimize the performance of the oxides as active electrode materials in lithium cells. The manganese-cobalt mixed oxides obtained by this procedure were cubic or tetragonal phases depending on the cobalt content. SEM images showed spherical macroporous aggregates for MnCo 2 O 4 and hollow spheres for manganese oxides. The galvanostatic cycling of lithium cells assembled with these materials demonstrated a simultaneous reduction of cobalt and manganese during the first discharge and separation of cobalt- and manganese-based products on further cycling. As compared with binary manganese oxides, a notorious electrochemical improvement was observed in the mixed oxides. This behavior is a consequence of the synergistic effect of both transition metal elements, associated with the in-situ formation of a nanocomposite electrode material when cobalt is introduced in the manganese oxide composition. Values higher than 400 mAh/g were sustained after 50 cycles for MnCo 2 O 4

Soybean Root-Derived Hierarchical Porous Carbon as Electrode Material for High-Performance Supercapacitors in Ionic Liquids.

Science.gov (United States)

Guo, Nannan; Li, Min; Wang, Yong; Sun, Xingkai; Wang, Feng; Yang, Ru

2016-12-14

Soybeans are extensively cultivated worldwide as human food. However, large quantities of soybean roots (SRs), which possess an abundant three-dimensional (3D) structure, remain unused and produce enormous pressure on the environment. Here, 3D hierarchical porous carbon was prepared by the facile carbonization of SRs followed by chemical activation. The as-prepared material, possessing large specific surface area (2143 m 2 g -1 ), good electrical conductivity, and unique 3D hierarchical porosity, shows outstanding electrochemical performance as an electrode material for supercapacitors, such as a high capacitance (276 F g -1 at 0.5 A g -1 ), superior cycle stability (98% capacitance retention after 10,000 cycles at 5 A g -1 ), and good rate capability in a symmetric two-electrode supercapacitor in 6 M KOH. Furthermore, the maximum energy density of as-assembled symmetric supercapacitor can reach 100.5 Wh kg -1 in neat EMIM BF 4 . Moreover, a value of 40.7 Wh kg -1 is maintained at ultrahigh power density (63000 W kg -1 ). These results show that the as-assembled supercapacitor can simultaneously deliver superior energy and power density.

Direct Observation of Active Material Concentration Gradients and Crystallinity Breakdown in LiFePO4 Electrodes During Charge/Discharge Cycling of Lithium Batteries.

Science.gov (United States)

Roberts, Matthew R; Madsen, Alex; Nicklin, Chris; Rawle, Jonathan; Palmer, Michael G; Owen, John R; Hector, Andrew L

2014-04-03

The phase changes that occur during discharge of an electrode comprised of LiFePO 4 , carbon, and PTFE binder have been studied in lithium half cells by using X-ray diffraction measurements in reflection geometry. Differences in the state of charge between the front and the back of LiFePO 4 electrodes have been visualized. By modifying the X-ray incident angle the depth of penetration of the X-ray beam into the electrode was altered, allowing for the examination of any concentration gradients that were present within the electrode. At high rates of discharge the electrode side facing the current collector underwent limited lithium insertion while the electrode as a whole underwent greater than 50% of discharge. This behavior is consistent with depletion at high rate of the lithium content of the electrolyte contained in the electrode pores. Increases in the diffraction peak widths indicated a breakdown of crystallinity within the active material during cycling even during the relatively short duration of these experiments, which can also be linked to cycling at high rate.

Electronically conductive polymer binder for lithium-ion battery electrode

Energy Technology Data Exchange (ETDEWEB)

Liu, Gao; Xun, Shidi; Battaglia, Vincent S.; Zheng, Honghe; Wu, Mingyan

2017-08-01

A family of carboxylic acid groups containing fluorene/fluorenon copolymers is disclosed as binders of silicon particles in the fabrication of negative electrodes for use with lithium ion batteries. Triethyleneoxide side chains provide improved adhesion to materials such as, graphite, silicon, silicon alloy, tin, tin alloy. These binders enable the use of silicon as an electrode material as they significantly improve the cycle-ability of silicon by preventing electrode degradation over time. In particular, these polymers, which become conductive on first charge, bind to the silicon particles of the electrode, are flexible so as to better accommodate the expansion and contraction of the electrode during charge/discharge, and being conductive promote the flow battery current.

Electronically conductive polymer binder for lithium-ion battery electrode

Science.gov (United States)

Liu, Gao; Xun, Shidi; Battaglia, Vincent S.; Zheng, Honghe; Wu, Mingyan

2015-07-07

A family of carboxylic acid groups containing fluorene/fluorenon copolymers is disclosed as binders of silicon particles in the fabrication of negative electrodes for use with lithium ion batteries. Triethyleneoxide side chains provide improved adhesion to materials such as, graphite, silicon, silicon alloy, tin, tin alloy. These binders enable the use of silicon as an electrode material as they significantly improve the cycle-ability of silicon by preventing electrode degradation over time. In particular, these polymers, which become conductive on first charge, bind to the silicon particles of the electrode, are flexible so as to better accommodate the expansion and contraction of the electrode during charge/discharge, and being conductive promote the flow battery current.

International nuclear material safeguards

International Nuclear Information System (INIS)

Syed Azmi Syed Ali

1985-01-01

History can be a very dull subject if it relates to events which have long since lost their relevance. The factors which led to the creation of the International Atomic Energy Agency (IAEA), however, are as important and relevant today as they were when the Agency was first created. Without understanding these factors it is impossible to realise how important the Agency is in the present world or to understand some of the controversies surrounding its future. Central to these controversies is the question of how best to promote the international transfer of nuclear technology without contributing further to the problem of proliferating nuclear explosives or explosive capabilities. One effective means is to subject nuclear materials (see accompanying article in box), which forms the basic link between the manufacture of nuclear explosives and nuclear power generation, to international safeguards. This was realized very early in the development of nuclear power and was given greater emphasis following the deployment of the first two atomic bombs towards the end of World War II. (author)

Carbon/CuO nanosphere-anchored g-C3N4 nanosheets as ternary electrode material for supercapacitors

Science.gov (United States)

Vattikuti, S. V. Prabhakar; Reddy, B. Purusottam; Byon, Chan; Shim, Jaesool

2018-06-01

Novel electrode materials for supercapacitors comprised of carbon and copper oxide (CuO) nanospheres on graphitic carbon nitride (g-C3N4) nanosheets, denoted as C/CuO@g-C3N4 are self-assembled via a one-step co-pyrolysis decomposition method. The pure g-C3N4 and C/CuO@g-C3N4 were confirmed by powder X-ray diffraction (XRD), high-resolution transmission electron microscopy (HRTEM), thermal gravimetric and differential thermal analysis (TG-DTA), X-ray photoelectron spectroscopy (XPS), N2 adsorption/desorption studies and Fourier-transform infrared spectroscopy (FTIR). The specific capacitance was 247.2 F g-1 in 0.5 M NaOH at a current density of 1 A g-1, and more than 92.1% of the capacitance was retained after 6000 cycles. The property enhancement was ascribed to the synergistic effects of the three components in the composite. These results suggest that C/CuO@g-C3N4 possessed an excellent cyclic stability with respect to their capacity performance as electrode materials.

Inherent N,O-containing carbon frameworks as electrode materials for high-performance supercapacitors.

Science.gov (United States)

Hu, Fangyuan; Wang, Jinyan; Hu, Shui; Li, Linfei; Wang, Gang; Qiu, Jieshan; Jian, Xigao

2016-09-15

N,O-Containing micropore-dominated materials have been developed successfully via temperature-dependent cross-linking of 4,4'-(dioxo-diphenyl-2,3,6,7-tetraazaanthracenediyl)dibenzonitrile (DPDN) monomers. By employing a molecular engineering strategy, we have designed and synthesized a series of porous heteroatom-containing carbon frameworks (PHCFs), in which nitrogen and oxygen heteroatoms are distributed homogeneously throughout the whole framework at the atomic level, which can ensure the stability of its electrical properties. The as-made PHCFs@550 exhibits a high specific capacitance of 378 F g -1 , with an excellent long cycling life, including excellent cycling stability (capacitance retention of ca. 120% over 20 000 cycles). Moreover, the successful preparation of PHCFs provides new insights for the fabrication of nitrogen and oxygen-containing electrode materials from readily available components via a facile route.

Metallic 1T phase MoS2 nanosheets as supercapacitor electrode materials.

Science.gov (United States)

Acerce, Muharrem; Voiry, Damien; Chhowalla, Manish

2015-04-01

Efficient intercalation of ions in layered materials forms the basis of electrochemical energy storage devices such as batteries and capacitors. Recent research has focused on the exfoliation of layered materials and then restacking the two-dimensional exfoliated nanosheets to form electrodes with enhanced electrochemical response. Here, we show that chemically exfoliated nanosheets of MoS2 containing a high concentration of the metallic 1T phase can electrochemically intercalate ions such as H(+), Li(+), Na(+) and K(+) with extraordinary efficiency and achieve capacitance values ranging from ∼400 to ∼700 F cm(-3) in a variety of aqueous electrolytes. We also demonstrate that this material is suitable for high-voltage (3.5 V) operation in non-aqueous organic electrolytes, showing prime volumetric energy and power density values, coulombic efficiencies in excess of 95%, and stability over 5,000 cycles. As we show by X-ray diffraction analysis, these favourable electrochemical properties of 1T MoS2 layers are mainly a result of their hydrophilicity and high electrical conductivity, as well as the ability of the exfoliated layers to dynamically expand and intercalate the various ions.

Poly(3,4-ethylenedioxythiophene) nanotubes as electrode materials for a high-powered supercapacitor

International Nuclear Information System (INIS)

Liu Ran; Cho, Seung Il; Lee, Sang Bok

2008-01-01

We report the fast charging/discharging capability of poly(3,4-ethylenedioxythiophene) (PEDOT) nanotubes during the redox process and their potential application to a high-powered supercapacitor. PEDOT nanotubes were electrochemically synthesized in a porous alumina membrane, and their structures were characterized using electron microscopes. Cyclic voltammetry was used to characterize the specific capacitance of the PEDOT nanotubes at various scan rates. A type I supercapacitor (two symmetric electrodes) based on PEDOT nanotube electrodes was fabricated, and its energy density and power density were evaluated by galvanostatic charge/discharge cycles at various current densities. We show that the PEDOT-nanotube-based supercapacitor can achieve a high power density of 25 kW kg -1 while maintaining 80% energy density (5.6 W h kg -1 ). This high power capability is attributed to the fast charge/discharge of nanotubular structures: hollow nanotubes allow counter-ions to readily penetrate into the polymer and access their internal surfaces, while the thin wall provides a short diffusion distance to facilitate the ion transport. Impedance spectroscopy shows that nanotubes have much lower diffusional resistance to charging ions than solid nanowires shielded by an alumina template, providing supporting information for the high charging/discharging efficiency of nanotubular structures

Nuclear materials control and accountability internal audit program

International Nuclear Information System (INIS)

Barham, M.A.; Abbott, R.R.

1991-01-01

This paper reports that the Department of Energy Order (DOE) 5633.3, Control and Accountability for Nuclear Materials, includes several requirements for development and implementation of an internal audit program. Martin Marietta Energy System, Inc., manages five sites in Tennessee, Kentucky, and Ohio for the DOE Field Office, Oak Ridge and has a Central Nuclear Materials Control and Accountability (NMC and A) Manager with matrixed responsibility for the NMC and A program at the five sites. The Energy Systems Central NMC and A Manager has developed an NMC and A Internal Audit Handbook which defines the functional responsibilities, performance criteria, and reporting and documentation requirements for the Energy Systems NMC and A Internal Audit Program. The initial work to develop and implement these standards was tested at the K-25 Site when the site hired an internal auditor to meet the DOE requirements for an NMC and A Internal Audit program

A Difference in Using Atomic Layer Deposition or Physical Vapour Deposition TiN as Electrode Material in Metal-Insulator-Metal and Metal-Insulator-Silicon Capacitors

NARCIS (Netherlands)

Groenland, A.W.; Wolters, Robertus A.M.; Kovalgin, Alexeij Y.; Schmitz, Jurriaan

2011-01-01

In this work, metal-insulator-metal (MIM) and metal-insulator-silicon (MIS) capacitors are studied using titanium nitride (TiN) as the electrode material. The effect of structural defects on the electrical properties on MIS and MIM capacitors is studied for various electrode configurations. In the

Lithium-aluminum-iron electrode composition

Science.gov (United States)

Kaun, Thomas D.

1979-01-01

A negative electrode composition is presented for use in a secondary electrochemical cell. The cell also includes an electrolyte with lithium ions such as a molten salt of alkali metal halides or alkaline earth metal halides that can be used in high-temperature cells. The cell's positive electrode contains a a chalcogen or a metal chalcogenide as the active electrode material. The negative electrode composition includes up to 50 atom percent lithium as the active electrode constituent in an alloy of aluminum-iron. Various binary and ternary intermetallic phases of lithium, aluminum and iron are formed. The lithium within the intermetallic phase of Al.sub.5 Fe.sub.2 exhibits increased activity over that of lithium within a lithium-aluminum alloy to provide an increased cell potential of up to about 0.25 volt.

Preliminary results of the International Fusion Materials Irradiation Facility deuteron injector

Energy Technology Data Exchange (ETDEWEB)

Gobin, R.; Adroit, G.; Bogard, D.; Bourdelle, G.; Chauvin, N.; Delferriere, O.; Gauthier, Y.; Girardot, P.; Guiho, P.; Harrault, F.; Jannin, J. L.; Loiseau, D.; Mattei, P.; Roger, A.; Sauce, Y.; Senee, F.; Vacher, T. [Commissariat a l' Energie Atomique et aux Energie Alternatives, CEA/Saclay, DSM/IRFU, 91191-Gif/Yvette (France)

2012-02-15

In the framework of the IFMIF-EVEDA project (International Fusion Materials Irradiation Facility-Engineering Validation and Engineering Design Activities), CEA/IRFU is in charge of the design, construction, and characterization of the 140 mA continuous deuteron injector, including the source and the low energy beam line. The electron cyclotron resonance ion source which operates at 2.45 GHz is associated with a 4-electrode extraction system in order to minimize beam divergence at the source exit. Krypton gas injection is foreseen in the 2-solenoid low energy beam line. Such Kr injection will allow reaching a high level of space charge compensation in order to improve the beam matching at the radio frequency quadrupole (RFQ) entrance. The injector construction is now completed on the Saclay site and the first plasma and beam production has been produced in May 2011. This installation will be tested with proton and deuteron beams either in pulsed or continuous mode at Saclay before shipping to Japan. In this paper, after a brief description of the installation, the preliminary results obtained with hydrogen gas injection into the plasma chamber will be reported.

Flexible supercapacitor electrodes based on real metal-like cellulose papers.

Science.gov (United States)

Ko, Yongmin; Kwon, Minseong; Bae, Wan Ki; Lee, Byeongyong; Lee, Seung Woo; Cho, Jinhan

2017-09-14

The effective implantation of conductive and charge storage materials into flexible frames has been strongly demanded for the development of flexible supercapacitors. Here, we introduce metallic cellulose paper-based supercapacitor electrodes with excellent energy storage performance by minimizing the contact resistance between neighboring metal and/or metal oxide nanoparticles using an assembly approach, called ligand-mediated layer-by-layer assembly. This approach can convert the insulating paper to the highly porous metallic paper with large surface areas that can function as current collectors and nanoparticle reservoirs for supercapacitor electrodes. Moreover, we demonstrate that the alternating structure design of the metal and pseudocapacitive nanoparticles on the metallic papers can remarkably increase the areal capacitance and rate capability with a notable decrease in the internal resistance. The maximum power and energy density of the metallic paper-based supercapacitors are estimated to be 15.1 mW cm -2 and 267.3 μWh cm -2 , respectively, substantially outperforming the performance of conventional paper or textile-type supercapacitors.With ligand-mediated layer-by-layer assembly between metal nanoparticles and small organic molecules, the authors prepare metallic paper electrodes for supercapacitors with high power and energy densities. This approach could be extended to various electrodes for portable/wearable electronics.

Structural and Electronic Features of Sb-Based Electrode Materials: 121Sb Moessbauer Spectrometry

International Nuclear Information System (INIS)

Ionica, C. M.; Aldon, L.; Lippens, P. E.; Morato, F.; Olivier-Fourcade, J.; Jumas, J.-C.

2004-01-01

Lithium insertion mechanisms in two antimony based compounds: CoSb 3 and CoSb have been studied by means of 121 Sb Moessbauer spectrometry. Structural and electronic modifications induced by insertion of lithium have been characterised for different depths of discharge. In all cases the insertion mechanisms can be described from several steps. In the first step antimony is partially dispersed in the metallic matrix with amorphisation of the electrode material and in a second step we can observe the alloy forming (Li 3 Sb). However this amorphous alloy remains in interaction with the matrix allowing then a good reversibility.

Nitrogen and oxygen co-doped carbon nanofibers with rich sub-nanoscale pores as self-supported electrode material of high-performance supercapacitors

International Nuclear Information System (INIS)

Li, Qun; Xie, Wenhe; Liu, Dequan; Wang, Qi; He, Deyan

2016-01-01

Self-supported porous carbon nanofibers (CNFs) network has been prepared by electrospinning technology assisted with template method. The as-prepared material is rich in sub-nanoscale pores and nitrogen and oxygen functional groups, which can serve as a fast conductive network with abundant electrochemical active sites and greatly facilitates the transport of electrons and ions. When the porous CNFs network is used as an electrode for supercapacitor in a three electrode system, it displays a high capacitance of 233.1 F/g at 0.2 A/g, and a capacitance of 130.2 F/g even at 14 A/g. It maintains a capacitance of 154.0 F/g with 90.17% retention after 4000 cycles at 2 A/g. Moreover, the assembled symmetric supercapacitor not only exhibits excellent rate capability and cycle performance, but also delivers an energy density of 4.17 Wh/kg and a power density of 2500 W/kg. The experimental results demonstrate that the prepared N, O co-doped carbon nanofibers with rich sub-nanoscale pores are a promising electrode material for high-performance supercapacitors.

Nitrogen-doped reduced graphene oxide electrodes for electrochemical supercapacitors.

Science.gov (United States)

Nolan, Hugo; Mendoza-Sanchez, Beatriz; Ashok Kumar, Nanjundan; McEvoy, Niall; O'Brien, Sean; Nicolosi, Valeria; Duesberg, Georg S

2014-02-14

Herein we use Nitrogen-doped reduced Graphene Oxide (N-rGO) as the active material in supercapacitor electrodes. Building on a previous work detailing the synthesis of this material, electrodes were fabricated via spray-deposition of aqueous dispersions and the electrochemical charge storage mechanism was investigated. Results indicate that the functionalised graphene displays improved performance compared to non-functionalised graphene. The simplicity of fabrication suggests ease of up-scaling of such electrodes for commercial applications.

Effective Chemical Route to 2D Nanostructured Silicon Electrode Material: Phase Transition from Exfoliated Clay Nanosheet to Porous Si Nanoplate

International Nuclear Information System (INIS)

Adpakpang, Kanyaporn; Patil, Sharad B.; Oh, Seung Mi; Kang, Joo-Hee; Lacroix, Marc; Hwang, Seong-Ju

2016-01-01

Graphical abstract: Effective morphological control of porous silicon 2D nanoplate can be achieved by the magnesiothermically-induced phase transition of exfoliated silicate clay nanosheets. The promising lithium storage performance of the obtained silicon materials with huge capacity and excellent rate characteristics underscores the prime importance of porously 2D nanostructured morphology of silicon. - Highlights: • 2D nanostructured silicon electrode materials are successfully synthesized via the magnesiothermically-induced phase transition of exfoliated clay 2D nanosheets. • High discharge capacity and rate capability are achieved from the 2D nanoplates of silicon. • Silicon 2D nanoplates can enhance both Li"+ diffusion and charge-transfer kinetics. • 2D nanostructured silicon is beneficial for the cycling stability by minimizing the volume change during lithiation-delithiation. - Abstract: An efficient and economical route for the synthesis of porous two-dimensional (2D) nanoplates of silicon is developed via the magnesiothermically-induced phase transition of exfoliated clay 2D nanosheets. The magnesiothermic reaction of precursor clay nanosheets prepared by the exfoliation and restacking with Mg"2"+ cations yields porous 2D nanoplates of elemental silicon. The variation in the Mg:SiO_2 ratio has a significant effect on the porosity and connectivity of silicon nanoplates. The porous silicon nanoplates show a high discharge capacity of 2000 mAh g"−"1 after 50 cycles. Of prime importance is that this electrode material still retains a large discharge capacity at higher C-rates, which is unusual for the elemental silicon electrode. This is mainly attributed to the improved diffusion of lithium ions, charge-transfer kinetics, and the preservation of the electrical connection of the porous 2D plate-shaped morphology. This study highlights the usefulness of clay mineral as an economical and scalable precursor of high-performance silicon electrodes with

International Regulations for Transport of Radioactive Materials, History and Security

International Nuclear Information System (INIS)

EL-Shinawy, R.M.K.

2013-01-01

International Regulations for the transport of radioactive materials have been published by International Atomic Energy Agency (IAEA) since 1961. These Regulations have been widely adopted into national Regulations. Also adopted into different modal Regulations such as International Air Transport Association (IATA) and International Martime Organization (IMO). These Regulations provide standards for insuring a high level of safety of general public, transport workers, property and environment against radiation, contamination, criticality hazard and thermal effects associated with the transport of radioactive wastes and materials. Several reviews conducted in consultation with Member States (MS) and concerned international organizations, resulted in comprehensive revisions till now. Radioactive materials are generally transported by specialized transport companies and experts. Shippers and carriers have designed their transport operations to comply with these international Regulations. About 20 million consignments of radioactive materials take place around the world each year. These materials were used in different fields such as medicine, industry, agriculture, research, consumer product and electric power generation. After September 11,2001, the IAEA and MS have worked together to develop a new guidance document concerning the security in the transport of radioactive materials. IAEA have initiated activities to assist MS in addressing the need for transport security in a comprehensive manner. The security guidance and measures were mentioned and discussed. The transport security becomes more developed and integrated into national Regulations of many countries beside the safety Regulations. IAEA and other International organizations are working with MS to implement transport security programs such as guidance, training, security assessments and upgrade assistance in these fields.

National and international nuclear material monitoring

International Nuclear Information System (INIS)

Waddoups, I.G.

1996-01-01

The status of nuclear materials in both the U.S. and Former Soviet Union is changing based upon the execution of agreements relative to weapons materials production and weapon dismantlement. The result of these activities is that a considerably different emphasis is being placed on how nuclear materials are viewed and utilized. Even though much effort is being expended on the final disposition of these materials, the interim need for storage and security of the material is increasing. Both safety and security requirements exist to govern activities when these materials are placed in storage. These requirements are intended to provide confidence that the material is not being misused and that the storage operations are conducted safely. Both of these goals can be significantly enhanced if technological monitoring of the material is performed. This paper will briefly discuss the traditional manual methods of U.S. and international material monitoring and then present approaches and technology that are available to achieve the same goals under the evolving environment

Layer-by-layer self-assembled active electrodes for hybrid photovoltaic cells

Energy Technology Data Exchange (ETDEWEB)

Kniprath, Rolf

2008-11-18

Solar cells based on thin organic/inorganic heterofilms are currently in the focus of research, since they represent promising candidates for cost-efficient photovoltaic energy conversion. In this type of cells, charges are separated at a heterointerface between dissimilar electrode materials. These materials either absorb light themselves, or they are sensitized by an additional absorber layer at the interface. The present work investigates photovoltaic cells which are composed of nanoporous TiO{sub 2} combined with conjugated polymers and semiconductor quantum dots (QDs). The method of layer-by-layer self-assembly of oppositely charged nanoparticles and polymers is used for the fabrication of such devices. This method allows to fabricate nanoporous films with controlled thicknesses in the range of a few hundred nanometers to several micrometers. Investigations with scanning electron (SEM) and atomic force microscopy (AFM) reveal that the surface morphology of the films depends only on the chemical structure of the polyions used in the production process, and not on their molecular weight or conformation. From dye adsorption at the internal surface of the electrodes one can estimate that the internal surface area of a 1 {mu}m thick film is up to 120 times larger than the projection plane. X-ray photoelectron spectroscopy (XPS) is used to demonstrate that during the layer-by-layer self-assembly at least 40% of the TiO{sub 2} surface is covered with polymers. This feature allows to incorporate polythiophene derivatives into the films and to use them as sensitizers for TiO{sub 2}. Further, electrodes containing CdSe or CdTe quantum dots (QDs) as sensitizers are fabricated. For the fabrication of photovoltaic cells the layer-by-layer grown films are coated with an additional polymer layer, and Au back electrodes are evaporated on top. The cells are illuminated through transparent doped SnO{sub 2} front electrodes. The I/V curves of all fabricated cells show diode

Effect of Particle Size on Electrode Potential and Thermodynamics of Nanoparticles Electrode in Theory and Experiment

International Nuclear Information System (INIS)

Yunfeng, Yang; Yongqiang, Xue; Zixiang, Cui; Miaozhi, Zhao

2014-01-01

The particle size of electrode materials has a significant influence on the standard electrode potential and the thermodynamic properties of electrode reactions. In this paper, the size-dependent electrochemical thermodynamics has been theoretically investigated and successfully deduced electrochemical thermodynamics equations for nanoparticles electrode. At the same time, the electrode potential and thermodynamical properties of Ag 2 O/Ag nanoparticles electrode constructed by the solid and spherical Ag 2 O nanoparticles with different sizes further testified that the particle size of nanoparticles has a significant effect on electrochemical thermodynamics. The results show that the electrode potential depends on that of the smallest nanoparticle in a nanoparticles electrode which consisted of different particle sizes of nano-Ag 2 O. When the size of Ag 2 O nanoparticles reduces, the standard electrode potentials and the equilibrium constants of the corresponding electrode reactions increase, and the temperature coefficient, the mole Gibbs energy change, the mole enthalpy change and the mole entropy change decrease. Moreover, these physical quantities are all linearly related with the reciprocal of average particle size (r > 10 nm). The experimental regularities coincide with the theoretical equations

New Transparent Laser-Drilled Fluorine-doped Tin Oxide covered Quartz Electrodes for Photo-Electrochemical Water Splitting

International Nuclear Information System (INIS)

Hernández, Simelys; Tortello, Mauro; Sacco, Adriano; Quaglio, Marzia; Meyer, Toby; Bianco, Stefano; Saracco, Guido; Pirri, C. Fabrizio; Tresso, Elena

2014-01-01

Graphical abstract: - Highlights: • A new transparent, conductive and porous electrode was developed. • It has a high effective surface area available for catalyst molecules attachment. • It is an ideal support for testing new anodic and cathodic photoactive materials. • The proof-of-concept was achieved in an appositely designed water photo-electrolyzer. • The EIS technique was used as a very powerful tool to characterize the new designed electrode. - Abstract: A new-designed transparent, conductive and porous electrode was developed for application in a compact laboratory-scale proton exchange membrane (PEM) photo-electrolyzer. The electrode is made of a thin transparent quartz sheet covered with fluorine-doped tin oxide (FTO), in which an array of holes is laser-drilled to allow water and gas permeation. The electrical, morphological, optical and electrochemical characterization of the drilled electrodes is presented in comparison with a non-drilled one. The drilled electrode exhibits, in the visible region, a good transmittance (average value of 62%), a noticeable reflectance due to the light scattering effect of the hole-drilled internal region, and a higher effective surface area than the non-drilled electrode. The proof-of-concept of the applicability of the drilled electrode was achieved by using it as a support for a traditional photocatalyst (i.e. commercial TiO 2 nanoparticles). The latter, coupled with a polymeric electrolyte membrane (i.e.Nafion 117) and a Pt counter electrode, forms a transparent membrane electrode assembly (MEA), with a good conductivity, wettability and porosity. Electrochemical impedance spectroscopy (EIS) was used as a very powerful tool to gain information on the real active surface of the new drilled electrode and the main electrochemical parameters driving the charge transfer reactions on it. This new electrode architecture is demonstrated to be an ideal support for testing new anodic and cathodic photoactive

3D-printed conductive static mixers enable all-vanadium redox flow battery using slurry electrodes

Science.gov (United States)

Percin, Korcan; Rommerskirchen, Alexandra; Sengpiel, Robert; Gendel, Youri; Wessling, Matthias

2018-03-01

State-of-the-art all-vanadium redox flow batteries employ porous carbonaceous materials as electrodes. The battery cells possess non-scalable fixed electrodes inserted into a cell stack. In contrast, a conductive particle network dispersed in the electrolyte, known as slurry electrode, may be beneficial for a scalable redox flow battery. In this work, slurry electrodes are successfully introduced to an all-vanadium redox flow battery. Activated carbon and graphite powder particles are dispersed up to 20 wt% in the vanadium electrolyte and charge-discharge behavior is inspected via polarization studies. Graphite powder slurry is superior over activated carbon with a polarization behavior closer to the standard graphite felt electrodes. 3D-printed conductive static mixers introduced to the slurry channel improve the charge transfer via intensified slurry mixing and increased surface area. Consequently, a significant increase in the coulombic efficiency up to 95% and energy efficiency up to 65% is obtained. Our results show that slurry electrodes supported by conductive static mixers can be competitive to state-of-the-art electrodes yielding an additional degree of freedom in battery design. Research into carbon properties (particle size, internal surface area, pore size distribution) tailored to the electrolyte system and optimization of the mixer geometry may yield even better battery properties.

Bipolar Radiofrequency Ablation Using Dual Internally Cooled Wet Electrodes: Experimental Study in Ex Vivo Bovine Liver

Energy Technology Data Exchange (ETDEWEB)

Lee, Young Joon; Byun, Jae Young [Dept. of Radiology, Seoul St. Mary' s Hospital, The Catholic University of Korea, College of Medicine, Seoul (Korea, Republic of)

2012-11-15

To determine the optimized protocol for bipolar radiofrequency ablation (RFA), using dual internally cooled wet (ICW) electrodes in the ex vivo bovine liver. RFA was applied to the explanted bovine liver, using two 3 cm active tip electrodes with 3.5 cm spacing. A total of 25 ablation zones were created by five groups; group A: 70 W-20 minute (min), group B: 70 W-25 min, group C: 90 W-15 min, group D: 90 W-20 min, and group E: 90 W-25 min. We measured the total energy and size of ablation zones with a color of grey or pink. Statistical analysis was done using Kruskal Wallis test and Mann Whitney U-test. The mean energy, mean volume of ablation zone with grey and pink color of groups A to E were 16.7, 23.9, 16.7, 21.8, 29.2 kcal, 25.7, 34.3, 29.5, 36.2, 45.2 cm{sup 3}, and 60.0, 88.0, 71.5, 87.4, 104.5 cm{sup 3}, respectively. Those were significantly different (p < 0.05). The volume of ablation zone of group E with grey color was larger than groups A, B and C (p < 0.05). Bipolar RFA, using dual ICW electrodes, can produce a large ablation zone with the protocol of 90 W-25 min.

Bipolar Radiofrequency Ablation Using Dual Internally Cooled Wet Electrodes: Experimental Study in Ex Vivo Bovine Liver

International Nuclear Information System (INIS)

Lee, Young Joon; Byun, Jae Young

2012-01-01

To determine the optimized protocol for bipolar radiofrequency ablation (RFA), using dual internally cooled wet (ICW) electrodes in the ex vivo bovine liver. RFA was applied to the explanted bovine liver, using two 3 cm active tip electrodes with 3.5 cm spacing. A total of 25 ablation zones were created by five groups; group A: 70 W-20 minute (min), group B: 70 W-25 min, group C: 90 W-15 min, group D: 90 W-20 min, and group E: 90 W-25 min. We measured the total energy and size of ablation zones with a color of grey or pink. Statistical analysis was done using Kruskal Wallis test and Mann Whitney U-test. The mean energy, mean volume of ablation zone with grey and pink color of groups A to E were 16.7, 23.9, 16.7, 21.8, 29.2 kcal, 25.7, 34.3, 29.5, 36.2, 45.2 cm 3 , and 60.0, 88.0, 71.5, 87.4, 104.5 cm 3 , respectively. Those were significantly different (p < 0.05). The volume of ablation zone of group E with grey color was larger than groups A, B and C (p < 0.05). Bipolar RFA, using dual ICW electrodes, can produce a large ablation zone with the protocol of 90 W-25 min.

Printed optically transparent graphene cellulose electrodes

Science.gov (United States)

Sinar, Dogan; Knopf, George K.; Nikumb, Suwas; Andrushchenko, Anatoly

2016-02-01

Optically transparent electrodes are a key component in variety of products including bioelectronics, touch screens, flexible displays, low emissivity windows, and photovoltaic cells. Although highly conductive indium tin oxide (ITO) films are often used in these electrode applications, the raw material is very expensive and the electrodes often fracture when mechanically stressed. An alternative low-cost material for inkjet printing transparent electrodes on glass and flexible polymer substrates is described in this paper. The water based ink is created by using a hydrophilic cellulose derivative, carboxymethyl cellulose (CMC), to help suspend the naturally hydrophobic graphene (G) sheets in a solvent composed of 70% DI water and 30% 2-butoxyethanol. The CMC chain has hydrophobic and hydrophilic functional sites which allow adsorption on G sheets and, therefore, permit the graphene to be stabilized in water by electrostatic and steric forces. Once deposited on the functionalized substrate the electrical conductivity of the printed films can be "tuned" by decomposing the cellulose stabilizer using thermal reduction. The entire electrode can be thermally reduced in an oven or portions of the electrode thermally modified using a laser annealing process. The thermal process can reduce the sheet resistance of G-CMC films to < 100 Ω/sq. Experimental studies show that the optical transmittance and sheet resistance of the G-CMC conductive electrode is a dependent on the film thickness (ie. superimposed printed layers). The printed electrodes have also been doped with AuCl3 to increase electrical conductivity without significantly increasing film thickness and, thereby, maintain high optical transparency.

Preparation and electrochemical performance of polyaniline-based carbon nanotubes as electrode material for supercapacitor

International Nuclear Information System (INIS)

Yang Miaomiao; Cheng Bin; Song Huaihe; Chen Xiaohong

2010-01-01

Nitrogen-containing carbon nanotubes (CNTs) with open end and low specific surface area were prepared via the carbonization of polyaniline (PANI) nanotubes synthesized by a rapidly mixed reaction. On the basis of analyzing the morphologies and structures of the original and carbonized PANI nanotubes, the electrochemical properties of PANI-based CNTs obtained at different temperatures as electrode materials for supercapacitors using 30 wt.% aqueous solution of KOH as electrolyte were investigated by galvanostatic charge/discharge and cyclic voltammetry. It was found that the carbonized PANI nanotubes at 700 o C exhibit high specific capacitance of 163 F g -1 at a current density of 0.1 A g -1 and excellent rate capability in KOH solution. Using X-ray photoelectron spectroscopy measurement the nitrogen state and content in PANI-CNTs were analysed, which could play important roles for the enhancement of electrochemical performance. When the appropriate content of nitrogen is present, the presence of pyrrole or pyridone and quaternary nitrogen is beneficial for the improvement of electron mobility and the wettability of electrode.

Carbon nanofibers wrapped with zinc oxide nano-flakes as promising electrode material for supercapacitors.

Science.gov (United States)

Pant, Bishweshwar; Park, Mira; Ojha, Gunendra Prasad; Park, Juhyeong; Kuk, Yun-Su; Lee, Eun-Jung; Kim, Hak-Yong; Park, Soo-Jin

2018-07-15

A combination of electrospinning technique and hydrothermal process was carried out to fabricate zinc oxide nano-flakes wrapped carbon nanofibers (ZnO/CNFs) composite as an effective electrode material for supercapacitor. The morphology of the as-synthesized composite clearly revealed that the carbon nanofibers were successfully wrapped with ZnO nano-flakes. The electrochemical performance of the as-synthesized nanocomposite electrode was evaluated by the cyclic voltammetry (CV), galvanostatic charge-discharge (GDC), and electrochemical impedance spectroscopy (EIS), and compared with the pristine ZnO nanofibers. It was found that the composite exhibited a higher specific capacitance (260 F/g) as compared to pristine ZnO NFs (118 F/g) at the scan rate of 5 mV/s. Furthermore, the ZnO/CNFs composite also exhibited good capacity retention (73.33%). The obtained results indicated great potential applications of ZnO/CNFs composite in developing energy storage devices with high energy and power densities. The present work might provide a new route for utilizing ZnO based composites for energy storage applications. Copyright © 2018 Elsevier Inc. All rights reserved.

Novel ultrathin Bi2O3 nanowires for supercapacitor electrode materials with high performance

Science.gov (United States)

Qiu, Yongfu; Fan, Hongbo; Chang, Xueyi; Dang, Haifeng; Luo, Qun; Cheng, Zhiyu

2018-03-01

In this paper, the ultrathin Bi2O3 nanowires are synthesized by an oxidative metal vapor transport deposition technique. Their diameters and length are about 10 nm and several tens of micrometers, the growth direction is along [101] and the specific surface area is about 7.34 m2 g-1. The galvanostatic charge-discharge measurement results show that the specific capacitances of the Bi2O3 nanowires-based electrodes increase with the decrease of the current densities. The maximum capacitance is 691.3 F g-1 at the current density of 2.0 A g-1. The Ragone plot shows that the Bi2O3 nanowires has excellent supercapacitive performance. Moreover, the cyclic stability is measured by the galvanostatic charge/discharge technique at a constant current density of 10.0 A g-1 in 6.0 M KOH electrolyte. The results show the excellent capacitance retention of 75.5% over 3000 cycles. In a word, the Bi2O3 nanowires should be the ideal potential electrode materials for low-costing and effective electrochemical supercapacitors.

Preparation and electrochemical performance of polyaniline-based carbon nanotubes as electrode material for supercapacitor

Energy Technology Data Exchange (ETDEWEB)

Yang Miaomiao; Cheng Bin [State Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology, Beijing 100029 (China); Song Huaihe, E-mail: songhh@mail.buct.edu.c [State Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology, Beijing 100029 (China); Chen Xiaohong [State Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology, Beijing 100029 (China)

2010-09-30

Nitrogen-containing carbon nanotubes (CNTs) with open end and low specific surface area were prepared via the carbonization of polyaniline (PANI) nanotubes synthesized by a rapidly mixed reaction. On the basis of analyzing the morphologies and structures of the original and carbonized PANI nanotubes, the electrochemical properties of PANI-based CNTs obtained at different temperatures as electrode materials for supercapacitors using 30 wt.% aqueous solution of KOH as electrolyte were investigated by galvanostatic charge/discharge and cyclic voltammetry. It was found that the carbonized PANI nanotubes at 700 {sup o}C exhibit high specific capacitance of 163 F g{sup -1} at a current density of 0.1 A g{sup -1} and excellent rate capability in KOH solution. Using X-ray photoelectron spectroscopy measurement the nitrogen state and content in PANI-CNTs were analysed, which could play important roles for the enhancement of electrochemical performance. When the appropriate content of nitrogen is present, the presence of pyrrole or pyridone and quaternary nitrogen is beneficial for the improvement of electron mobility and the wettability of electrode.

Ceramic carbon electrode-based anodes for use in the copper-chlorine thermochemical cycle

International Nuclear Information System (INIS)

Ranganathan, S.; Easton, E.B.

2009-01-01

Sol-gel chemistry is becoming more popular for the synthesis of electrode materials. For example, the sol-gel reaction can be performed in the presence of a carbon black to form a ceramic carbon electrode (CCE). The resultant CCE structure contains electronically conductive carbon particle pathways that are bound together via the ceramic binder, which can also promote ion transport. Furthermore, the CCE structure has a high active surface area and is chemical and thermally robust. We have investigated CCE materials prepared using 3-aminopropyl trimethoxysilane. Electrochemical experiments (cyclic voltammetry, electrochemical impedance spectroscopy) were performed to characterize their suitability as anode electrode materials for use in the electrochemical step of the Cu-Cl thermochemical cycle. Our initial results have shown that CCE-based electrodes vastly outperform a bare carbon electrode, and thus are highly promising and cost-effective electrode material. Subsequent experiments involved the manipulation of the relative ratio of organosilane carbon precursors to gauge its impact on electrode properties and performance. An overview of the materials characterization and electrochemical measurements will be presented. (author)

Ceramic carbon electrode-based anodes for use in the copper-chlorine thermochemical cycle

Energy Technology Data Exchange (ETDEWEB)

Ranganathan, S.; Easton, E.B. [Faculty of Science, Univ. of Ontario Inst. of Technology, Oshawa, Ontario (Canada)], E-mail: ranga@uoit.ca, Brad.Easton@uoit.ca

2009-07-01

Sol-gel chemistry is becoming more popular for the synthesis of electrode materials. For example, the sol-gel reaction can be performed in the presence of a carbon black to form a ceramic carbon electrode (CCE). The resultant CCE structure contains electronically conductive carbon particle pathways that are bound together via the ceramic binder, which can also promote ion transport. Furthermore, the CCE structure has a high active surface area and is chemical and thermally robust. We have investigated CCE materials prepared using 3-aminopropyl trimethoxysilane. Electrochemical experiments (cyclic voltammetry, electrochemical impedance spectroscopy) were performed to characterize their suitability as anode electrode materials for use in the electrochemical step of the Cu-Cl thermochemical cycle. Our initial results have shown that CCE-based electrodes vastly outperform a bare carbon electrode, and thus are highly promising and cost-effective electrode material. Subsequent experiments involved the manipulation of the relative ratio of organosilane carbon precursors to gauge its impact on electrode properties and performance. An overview of the materials characterization and electrochemical measurements will be presented. (author)

Monitoring drilling mud composition using flowing liquid junction electrodes

Energy Technology Data Exchange (ETDEWEB)

Jasinski, R; Fletcher, P; Vercaemer, C

1990-06-27

The concentration of a chosen ionic component of a drilling mud is determined from the potential difference between an ion selective electrode, selective to the component and a reference electrode, the reference electrode being connected to the mud by a liquid junction through which reference electrolyte flows from the electrode to the mud. The system avoids errors due to undesirable interactions between the mud and the reference electrode materials. (author).

Study of the collecting electrode material of an extrapolation chamber by Monte Carlo simulation; Estudo do material do eletrodo coletor de uma câmara de extrapolação por simulação de Monte Carlo

Energy Technology Data Exchange (ETDEWEB)

Vedovato, Uly Pita; Santos, William S.; Perini, Ana Paula, E-mail: anapaula.perini@ufu.br [Universidade Federal de Uberlândia (INFIS/UFU), Uberlândia, MG (Brazil). Instituto de Física; Neves, Lucio Pereira; Caldas, Linda V. E. [Instituto de Pesquisas Energéticas e Nucleares (IPEN/CNEN-SP), São Paulo, SP (Brazil); Belinato, Walmir [Instituto Federal de Educação, Ciência e Tecnologia da Bahia (IFBA), Vitória da Conquista, BA (Brazil)

2017-07-01

In this work, the influence of different materials of the collecting electrode on the response of an extrapolation ionization chamber, was evaluated. This ionization chamber was simulated with the MCNP-4C Monte Carlo code and the spectrum of a standard diagnostic radiology beam (RQR5) was utilized. The different results are due to interactions of photons with different materials of the collecting electrode contributing with different values of energy deposited in the sensitive volume of the ionization chamber, which depends on the atomic number of the evaluated materials. The material that presented the least influence was graphite, the original constituent of the ionization chamber. (author)

Computer Simulations of Composite Electrodes in Solid-Oxide Fuel-Cells

Energy Technology Data Exchange (ETDEWEB)

Sunde, Svein

1999-07-01

Fuel cells are devices for converting the combined chemical (free) energy of fuels and oxygen (air) directly to electrical energy without relying on the dynamic action of steam heated by reacting fuel-oxygen mixtures, like in steam turbines, or of the reacting gas mixtures themselves, like in gas turbines. The basic rationale for fuel cells is their high efficiencies as compared to indirect-conversion methods. Fuel cells are currently being considered for a number of applications, among them de-centralised power supply. Fuel cells come in five basic types and are usually classified according to the type of electrolyte used, which in turn to a significant degree limits the options for anode and cathode materials. The solid-oxide fuel-cell (SOFC) , with which this thesis is concerned, is thus named after its oxide electrolyte, typically the oxide-ion conducting material yttria-stabilised zirconia (YSZ). While the cathode of an SOFC is often uniform in chemical composition (or at least intended to be), various problems of delamination, cracking etc. associated with the use of metallic anode electrocatalysts led to the development of composite SOFC anodes. Porous anodes consisting of Ni and YSZ particles in roughly 50/50 wt-% mixtures are now almost standard with any SOFC-development programme. The designer of composite SOFC electrodes is faced with at least three, interrelated questions: (1) What will be the optimum microstructure and composition of the composite electrode? (2) If the structure changes during operation, as is often observed, what will be the consequences for the internal losses in the cell? (3) How do we interpret electrochemical and conductivity measurements with regard to structure and composition? It is the primary purpose of this thesis to provide a framework for modelling the electrochemical and transport properties of composite electrodes for SOFC, and to arrive at some new insights that cannot be offered by experiment alone. Emphasis is put on

The effect of gamma radiation on reference electrodes and platinum and carbon steel bare metal electrodes in a simulated waste solution

International Nuclear Information System (INIS)

Danielson, M.J.

1993-09-01

Electrochemical potential measurements of materials in waste tanks are important in determining if the materials have a propensity for stress corrosion cracking and pitting. Potential measurement requires a reference electrode, but the effect of radiation on the potential generated by the reference electrode has been an unknown quantity. To determine the significance of the radiation effect, Pacific Northwest Laboratory conducted studies of five types of electrodes under gamma radiation at room temperature. The subjects were two types of silver/silver chloride reference electrodes (Fisher and Lazaran), a mercury/calomel reference electrode, a platinum ''flag,'' and a piece of A-537 carbon steel; the electrodes were exposed to a simulated caustic tank environment. The Fisher silver/silver chloride and mercury/calomel reference electrodes showed essentially no radiation effects up to a flux of 2.1E6 R/h and fluence of 9.4E8 R, indicating they would be useful reference electrodes for in-tank studies. The Lazaran reg-sign silver/silver chloride electrode showed serious potential deviations at fluences of 2.E8 R, but it would be the electrode of choice in many situations because it is simple to maintain. Radiation affected the open circuit potential of both the platinum and carbon steel electrodes. This effect indicates that corrosion studies without radiation may not duplicate the corrosion processes expected in a waste tank. Mixed-potential theory was used to explain the radiation effects

Ionic Liquid Directed Mesoporous Carbon Nanoflakes as an Effiencient Electrode material

Science.gov (United States)

Kong, Lirong; Chen, Wei

2015-12-01

Supercapacitors are considered to be the most promising approach to meet the pressing requirements for energy storage devices. The electrode materials for supercapacitors have close relationship with their electrochemical properties and thus become the key point to improve their energy storage efficiency. Herein, by using poly (vinylidene fluoride-co-hexafluoropropylene) and ionic liquid as the dual templates, polyacrylonitrile as the carbon precursor, a flake-like carbon material was prepared by a direct carbonization method. In this method, poly (vinylidene fluoride-co-hexafluoropropylene) worked as the separator for the formation of isolated carbon flakes while aggregated ionic liquid worked as the pore template. The obtained carbon flakes exhibited a specific capacitance of 170 F/g at 0.1 A/g, a high energy density of 12.2 Wh/kg and a high power density of 5 kW/kg at the current of 10 A/g. It also maintained a high capacitance retention capability with almost no declination after 500 charge-discharge cycles. The ionic liquid directed method developed here also provided a new idea for the preparation of hierarchically porous carbon nanomaterials.

An environment-friendly route to synthesize reduced graphene oxide as a supercapacitor electrode material

International Nuclear Information System (INIS)

Zhang Dacheng; Zhang Xiong; Chen Yao; Wang Changhui; Ma Yanwei

2012-01-01

A large-scale, environment-friendly method to produce water-soluble reduced graphene oxide by using glutathione as a reducing and stabilization agent has been developed. The results of UV–visible absorption spectroscopy, X-ray photoelectron spectroscopy, atomic force microscopy, and transmission electron microscopy indicate that graphene oxide is reduced to graphene nanosheets which are single-layers and exhibit good dispersion in water. A reaction mechanism is proposed. The electrochemical properties of the graphene nanosheets as electrode materials for supercapacitors are studied by cyclic voltammetry and galvanostatic charge/discharge tests. A maximum specific capacitance of 238 F g −1 in a 1 M H 2 SO 4 electrolyte has been obtained. Meanwhile, the material shows excellent long-term cycle stability along with the retention of 97% for specific capacitance after 1000 cycle tests.

Direct Electrochemistry of Horseradish Peroxidase on NiO Nanoflower Modified Electrode and Its Electrocatalytic Activity

Directory of Open Access Journals (Sweden)

Lijun Yan

2016-09-01

Full Text Available In this paper nickel oxide (NiO nanoflower was synthesized and used for the realization of direct electrochemistry of horseradish peroxidase (HRP. By using carbon ionic liquid electrode (CILE as the substrate electrode, NiO-HRP composite was casted on the surface of CILE with chitosan (CTS as the film forming material and the modified electrode was denoted as CTS/NiO-HRP/CILE. UV-Vis absorption and FT-IR spectra confirmed that HRP retained its native structure after mixed with NiO nanoflower. Direct electron transfer of HRP on the modified electrode was investigated by cyclic voltammetry with a pair of quasi-reversible redox waves appeared, indicating that the presence of NiO nanoflower on the electrode surface could accelerate the electron transfer rate between the electroactive center of HRP and the substrate electrode. Electrochemical behaviors of HRP on the modified electrode were carefully investigated. The HRP modified electrode showed excellent electrocatalytic activity to the reduction of trichloroacetic acid with wider linear range and lower detection limit. Therefore the presence of NiO nanoflower could provide a friendly biocompatible interface for immobilizing biomolecules and keeping their native structure. The fabricated electrochemical biosensor displayed the advantages such as high sensitivity, good reproducibility and long-term stability. This work is licensed under a Creative Commons Attribution 4.0 International License.

Facilely synthesized Fe{sub 2}O{sub 3}–graphene nanocomposite as novel electrode materials for supercapacitors with high performance

Energy Technology Data Exchange (ETDEWEB)

Wang, Zhuo; Ma, Chunyan; Wang, Hailin [Department of Environmental Nano-Materials, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085 (China); Liu, Zonghuai [Key Laboratory of Applied Surface and Colloid Chemistry (Shaanxi Normal University), Ministry of Education, Xi’an 710062 (China); School of Materials Science and Engineering, Shaanxi Normal University, Xi’an 710062 (China); Hao, Zhengping, E-mail: zpinghao@rcees.ac.cn [Department of Environmental Nano-Materials, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085 (China)

2013-03-05

Graphical abstract: Fe{sub 2}O{sub 3}Graphene nanocomposite was synthesized in a simple hydrothermal way by using urea to adjust the system pH value, by this method the reduction of graphite oxide and the formation of Fe{sub 2}O{sub 3} nanocomposite are finished in one step. The specific capacitance of the Fe{sub 2}O{sub 3}Graphene electrode reached 226 F/g at a discharge current density of 1 A g{sup –1}. Highlights: ► The Fe{sub 2}O{sub 3}–graphene nanocomposite was obtained by friendly method with urea in one step. ► The addition of Fe{sub 2}O{sub 3} composites has positive effect on the electrical performance of the graphene nanosheets. ► The specific capacitance of the Fe{sub 2}O{sub 3}–graphene electrode was 226 F/g at a discharge current density of 1 A g{sup −1}. -- Abstract: Fe{sub 2}O{sub 3}–graphene nanocomposite with high capacitive properties had been prepared friendly and facilely by hydrothermal method in one-step. The morphology and structure of the obtained material were examined by X-ray diffraction (XRD), Brunauer–Emmett–Teller (BET) and transmission electron microscope (TEM) techniques. It was revealed by TEM images that Fe{sub 2}O{sub 3} nanoparticles grow well on the surface of graphene and the formation of Fe{sub 2}O{sub 3} nanoparticles hinders the aggregation of graphene (reduced graphene oxide, namely, RGO). Electrochemical properties of the synthesized materials were characterized by serials of electrochemical measurements in 1 M Na{sub 2}SO{sub 4} electrolyte. Fe{sub 2}O{sub 3}–graphene nanocomposite electrode show higher specific capacitance than graphene, indicating an accelerative effect of Fe{sub 2}O{sub 3} and graphene on improving the electrochemical performance of the electrode. The specific capacitance of Fe{sub 2}O{sub 3}–graphene nanocomposite is 226 F/g at a current density of 1 A/g. These attractive results indicate it is possible to seek and develop the promising, environmentally benign and commercial

A facile approach to anchor cadmium sulfide nanoparticles on graphene nanosheets as promising electrode materials

Energy Technology Data Exchange (ETDEWEB)

Yang, Jia; Li, Jing; Yang, Xuyu [Faculty of Materials Science and Engineering, Hubei University, Wuhan 430062 (China); Wang, Xianbao, E-mail: wangxb68@yahoo.com.cn [Faculty of Materials Science and Engineering, Hubei University, Wuhan 430062 (China); Ministry-of-Education Key Laboratory for the Green Preparation and Application of Functional Materials, Hubei University, Wuhan 430062 (China); Wan, Li; Yang, Yingkui [Faculty of Materials Science and Engineering, Hubei University, Wuhan 430062 (China)

2012-08-15

A controllable preparation of novel graphene-based inorganic semi-conducting composites has aroused great attention in the optoelectronic device and powerful electronic anode materials. In this article, we demonstrate a simple two-step strategy for the synthesis of cadmium sulfide/reduced graphene oxide (CdS/RGO) nanocomposites, of which the preparing process includes modification of the exfoliated graphene oxide acylated with thionyl chloride, immobilization of the CdS nanoparticles on the graphene oxide (GO) surface by an amide reaction between the amino groups located on the CdS particles and the acyl chloride bound to the GO surface, and reduction by hydrazine and ammonia. Our results showed that the CdS nanoparticles with an average size of 20 nm were homogeneously dispersed on the surface of RGO sheets. The CdS/RGO nanocomposites can form a homogeneous and stable solution in dimethylformamide, and CV analysis indicated a remarkable increase for the CdS/RGO modified electrode in the electrochemical current relative to that at a glass carbon electrode. -- Highlights: Black-Right-Pointing-Pointer CdS/RGO nanocomposites were synthesized by a covalent bonding and electrostatic interaction. Black-Right-Pointing-Pointer CdS/RGO exhibits a homogeneous dispersion in dimethylformamide. Black-Right-Pointing-Pointer CdS/RGO was used as an anode electrode with good electrochemical activity.

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