WorldWideScience

Sample records for high lithium pwr

  1. Lithium and boron analysis by LA-ICP-MS results from a bowed PWR rod with contact

    Directory of Open Access Journals (Sweden)

    Puranen Anders

    2017-01-01

    Full Text Available A previously published investigation of an irradiated fuel rod from the Ringhals 2 PWR, which was bowed to contact with an adjacent rod, identified a significant but highly localised thinning of the clad wall and increased corrosion. Rod fretting was deemed unlikely due to the adhering oxide covering the surfaces. Local overheating in itself was also deemed insufficient to account for the accelerated corrosion. Instead, an enhanced concentration of lithium due to conditions of local boiling was hypothesised to explain the accelerated corrosion. Studsvik has developed a hot cell coupled LA-ICP-MS (Laser Ablation Inductively Coupled Plasma Mass Spectrometer equipment that enables a flexible means of isotopic analysis of irradiated fuel and other highly active surfaces. In this work, the equipment was used to investigate the distribution of lithium (7Li and boron (11B in the outer oxide at the bow contact area. Depth profiling in the clad oxide at the opposite side of the rod to the point of contact, which is considered to have experienced normal operating conditions and which has a typical oxide thickness, evidenced levels of ∼10–20 ppm 7Li and a 11B content reaching hundreds of ppm in the outer parts of the oxide, largely in agreement with the expected range of Li and B clad oxide concentrations from previous studies. In the contact area, the 11B content was similar to the reference condition at the opposite side. The 7Li content in the outermost oxide closest to the contact was, however, found to be strongly elevated, reaching several hundred ppm. The considerable and highly localised increase in lithium content at the area of enhanced corrosion thus offers strong evidence for a case of lithium induced breakaway corrosion during power operation, when rod-to-rod contact and high enough surface heat flux results in a very local increase in lithium concentration.

  2. Automatic control of the lithium concentration of the reactor coolant in PWR plants

    Energy Technology Data Exchange (ETDEWEB)

    Long, A.; Bruere, X. [Framatome ANP, Paris (France); Cohen, J. [Electricite de France-DIS-CIPN, Marseille (France); Berger, M. [Electricite de France-DIS-SEPTEN, Villeurbanne (France)

    2002-07-01

    Given the specific operating mode of French units, observance of the lithium-boron diagram and consequently observance of reactor coolant pH is considered to be a priority relative to management of {sup 7}Li ({sup 7}Li recycling practices or prototypes). For this reason EDF and FRAMATOME-ANP have developed an automatic lithium hydroxide injection device, which serves to compensate in real time whenever the upper or lower limits of the lithium-boron diagram are exceeded and to prevent excursion at low pH. A prototype of this device is installed on unit N 2 of Tricastin NPP. The purpose of this document is to describe its principles and the main characteristics, to provide experience feedback on its operation and to present its potential. (author)

  3. Depletion of gadolinium burnable poison in a PWR assembly with high burnup fuel

    Energy Technology Data Exchange (ETDEWEB)

    Refeat, Riham Mahmoud [Nuclear and Radiological Regulatory Authority (NRRA), Cairo (Egypt). Safety Engineering Dept.

    2015-12-15

    A tendency to increase the discharge burnup of nuclear fuel for Advanced Pressurized Water Reactors (PWR) has been a characteristic of its operation for many years. It will be able to burn at very high burnup of about 70 GWd/t with UO{sub 2} fuels. The U-235 enrichment must be higher than 5 %, which leads to the necessity of using an extremely efficient burnable poison like Gadolinium oxide. Using gadolinium isotope is significant due to its particular depletion behavior (''Onion-Skin'' effect). In this paper, the MCNPX2.7 code is used to calculate the important neutronic parameters of the next generation fuels of PWR. K-infinity, local peaking factor and fission rate distributions are calculated for a PWR assembly which burn at very high burnup reaching 70 GWd/t. The calculations are performed using the recently released evaluated Gadolinium cross section data. The results obtained are close to those of a LWR next generation fuel benchmark problem. This demonstrates that the calculation scheme used is able to accurately model a PWR assembly that operates at high burnup values.

  4. Irradiation and lithium presence influence on the crystallographic nature of zirconia in the framework of PWR zircaloy 4 fuel cladding corrosion study; Influence de l'irradiation et de la presence du lithium sur la nature cristallographique de la zircone dans le cadre de l'etude de la corrosion du zircaloy 4 en milieu reacteur a eau pressurisee

    Energy Technology Data Exchange (ETDEWEB)

    Gibert, C

    1999-07-01

    The-increasing deterioration of the initially protective zirconia layer is one of the hypotheses which can explain the impairment with time of PWR fuel cladding corrosion. This deterioration could be worsened by irradiation or lithium presence in the oxidizing medium. The aim of this thesis was to underline the influence of those two parameters on zirconia crystallographic nature. We first studied the impact of ionic irradiation on pure, powdery, monoclinic zirconia and oxidation formed zirconia, mainly with X-ray diffraction and Raman microscopy. The high or low energy particles used (Kr{sup n+-}, Ar{sup n+}) respectively favored electronic or atomic defaults production. The crystallographic analyses showed that these irradiation have a significant effect on zirconia by inducing nucleation or growth of tetragonal phase. The extent depends on sample nature and particles energy. In all cases, phase transformation is correlated with crystalline parameters, grain size and especially micro-stress changes. The results are consistent with those obtained with 1 to 5 cycles PWR claddings. Therefore, the corrosion acceleration observed in reactor can partly be explained by the stress fields appearance under irradiation, which is particularly detrimental to zirconia layer cohesion. Last, we have underlined that the presence of considerable amounts of lithium in the oxidizing medium ((> 700 ppm) induces the disappearance of the tetragonal zirconia located at the metal/oxide interface and the appearance of a porosity of the dense under layer, which looses its protectiveness. (author)

  5. A highly heterogeneous 3D PWR core benchmark: deterministic and Monte Carlo method comparison

    Science.gov (United States)

    Jaboulay, J.-C.; Damian, F.; Douce, S.; Lopez, F.; Guenaut, C.; Aggery, A.; Poinot-Salanon, C.

    2014-06-01

    Physical analyses of the LWR potential performances with regards to the fuel utilization require an important part of the work dedicated to the validation of the deterministic models used for theses analyses. Advances in both codes and computer technology give the opportunity to perform the validation of these models on complex 3D core configurations closed to the physical situations encountered (both steady-state and transient configurations). In this paper, we used the Monte Carlo Transport code TRIPOLI-4®; to describe a whole 3D large-scale and highly-heterogeneous LWR core. The aim of this study is to validate the deterministic CRONOS2 code to Monte Carlo code TRIPOLI-4®; in a relevant PWR core configuration. As a consequence, a 3D pin by pin model with a consistent number of volumes (4.3 millions) and media (around 23,000) is established to precisely characterize the core at equilibrium cycle, namely using a refined burn-up and moderator density maps. The configuration selected for this analysis is a very heterogeneous PWR high conversion core with fissile (MOX fuel) and fertile zones (depleted uranium). Furthermore, a tight pitch lattice is selcted (to increase conversion of 238U in 239Pu) that leads to harder neutron spectrum compared to standard PWR assembly. In these conditions two main subjects will be discussed: the Monte Carlo variance calculation and the assessment of the diffusion operator with two energy groups for the core calculation.

  6. High energy density lithium batteries

    CERN Document Server

    Aifantis, Katerina E; Kumar, R Vasant

    2010-01-01

    Cell phones, portable computers and other electronic devices crucially depend on reliable, compact yet powerful batteries. Therefore, intensive research is devoted to improving performance and reducing failure rates. Rechargeable lithium-ion batteries promise significant advancement and high application potential for hybrid vehicles, biomedical devices, and everyday appliances. This monograph provides special focus on the methods and approaches for enhancing the performance of next-generation batteries through the use of nanotechnology. Deeper understanding of the mechanisms and strategies is

  7. Application of LBB to high energy piping systems in operating PWR

    Energy Technology Data Exchange (ETDEWEB)

    Swamy, S.A.; Bhowmick, D.C. [Westinghouse Nuclear Technology Division, Pittsburgh, PA (United States)

    1997-04-01

    The amendment to General Design Criterion 4 allows exclusion, from the design basis, of dynamic effects associated with high energy pipe rupture by application of leak-before-break (LBB) technology. This new approach has resulted in substantial financial savings to utilities when applied to the Pressurized Water Reactor (PWR) primary loop piping and auxiliary piping systems made of stainless steel material. To date majority of applications pertain to piping systems in operating plants. Various steps of evaluation associated with the LBB application to an operating plant are described in this paper.

  8. Effects of Lower Drying-Storage Temperature on the Ductility of High-Burnup PWR Cladding

    Energy Technology Data Exchange (ETDEWEB)

    Billone, M. C. [Argonne National Lab. (ANL), Argonne, IL (United States); Burtseva, T. A. [Argonne National Lab. (ANL), Argonne, IL (United States)

    2016-08-30

    The purpose of this research effort is to determine the effects of canister and/or cask drying and storage on radial hydride precipitation in, and potential embrittlement of, high-burnup (HBU) pressurized water reactor (PWR) cladding alloys during cooling for a range of peak drying-storage temperatures (PCT) and hoop stresses. Extensive precipitation of radial hydrides could lower the failure hoop stresses and strains, relative to limits established for as-irradiated cladding from discharged fuel rods stored in pools, at temperatures below the ductile-to-brittle transition temperature (DBTT).

  9. Analysis of bubble pressure in the rim region of high burnup PWR fuel

    Energy Technology Data Exchange (ETDEWEB)

    Koo, Yang Hyun; Lee, Byung Ho; Sohn, Dong Seong [Korea Atomic Energy Research Institute, Taejeon (Korea)

    2000-02-01

    Bubble pressure in the rim region of high burnup PWR UO{sub 2} fuel has been modeled based on measured rim width, porosity and bubble density. Using the assumption that excessive bubble pressure in the rim is inversely proportional to its radius, proportionality constant is derived as a function of average pellet burnup and bubble radius. This approach is possible because the integration of the number of Xe atoms retained in the rim bubbles, which can be calculated as a function of bubble radius, over the bubble radius gives the total number of Xe atoms in the rim bubbles. Here the total number of Xe atoms in the rim bubbles can be derived from the measured Xe depletion fraction in the matrix and the calculated rim thickness. Then the rim bubble pressure is obtained as a function of fuel burnup and bubble size from the proportionality constant. Therefore, the present model can provide some useful information that would be required to analyze the behavior of high burnup PWR UO{sub 2} fuel under both normal and transient operating conditions. 28 refs., 9 figs. (Author)

  10. New aluminium alloys with high lithium content

    Energy Technology Data Exchange (ETDEWEB)

    Schemme, K.; Velten, B.

    1989-06-01

    Since the early 80's there have been made great efforts to replace the high strength aluminium alloys for the aircraft and space industry by a new generation of aluminium-lithium alloys. The attractivity of this kind of alloys could be increased by a further reduction of their density, caused by an increasing lithium content (/ge/ 5 wt.% Li). Therefore binary high-lithium containing alloys with low density are produced and metallografically investigated. A survey of their strength and wear behavior is given by using tensile tests and pin abrasing tests. (orig.).

  11. Fuel failure and fission gas release in high burnup PWR fuels under RIA conditions

    Science.gov (United States)

    Fuketa, Toyoshi; Sasajima, Hideo; Mori, Yukihide; Ishijima, Kiyomi

    1997-09-01

    To study the fuel behavior and to evaluate the fuel enthalpy threshold of fuel rod failure under reactivity initiated accident (RIA) conditions, a series of experiments using pulse irradiation capability of the Nuclear Safety Research Reactor (NSRR) has been performed. During the experiments with 50 MWd/kg U PWR fuel rods (HBO test series; an acronym for high burnup fuels irradiated in Ohi unit 1 reactor), significant cladding failure occurred. The energy deposition level at the instant of the fuel failure in the test is 60 cal/g fuel, and is considerably lower than those expected and pre-evaluated. The result suggests that mechanical interaction between the fuel pellets and the cladding tube with decreased integrity due to hydrogen embrittlement causes fuel failure at the low energy deposition level. After the pulse irradiation, the fuel pellets were found as fragmented debris in the coolant water, and most of these were finely fragmented. This paper describes several key observations in the NSRR experiments, which include cladding failure at the lower enthalpy level, possible post-failure events and large fission gas release.

  12. Identification of dose-reduction techniques for BWR and PWR repetitive high-dose jobs

    Energy Technology Data Exchange (ETDEWEB)

    Dionne, B.J.; Baum, J.W.

    1984-01-01

    As a result of concern about the apparent increase in collective radiation dose to workers at nuclear power plants, this project will provide information to industry in preplanning for radiation protection during maintenance operations. This study identifies Boiling Water Reactor (BWR) and Pressurized Water Reactor (PWR) repetitive jobs, and respective collective dose trends and dose reduction techniques. 3 references, 2 tables. (ACR)

  13. Lithium-Based High Energy Density Flow Batteries

    Science.gov (United States)

    Bugga, Ratnakumar V. (Inventor); West, William C. (Inventor); Kindler, Andrew (Inventor); Smart, Marshall C. (Inventor)

    2014-01-01

    Systems and methods in accordance with embodiments of the invention implement a lithium-based high energy density flow battery. In one embodiment, a lithium-based high energy density flow battery includes a first anodic conductive solution that includes a lithium polyaromatic hydrocarbon complex dissolved in a solvent, a second cathodic conductive solution that includes a cathodic complex dissolved in a solvent, a solid lithium ion conductor disposed so as to separate the first solution from the second solution, such that the first conductive solution, the second conductive solution, and the solid lithium ionic conductor define a circuit, where when the circuit is closed, lithium from the lithium polyaromatic hydrocarbon complex in the first conductive solution dissociates from the lithium polyaromatic hydrocarbon complex, migrates through the solid lithium ionic conductor, and associates with the cathodic complex of the second conductive solution, and a current is generated.

  14. High-Cycle-Life Lithium Cell

    Science.gov (United States)

    Yen, S. P. S.; Carter, B.; Shen, D.; Somoano, R.

    1985-01-01

    Lithium-anode electrochemical cell offers increased number of charge/ discharge cycles. Cell uses components selected for compatibility with electrolyte solvent: These materials are wettable and chemically stable. Low vapor pressure and high electrochemical stability of solvent improve cell packaging, handling, and safety. Cell operates at modest temperatures - less than 100 degrees C - and is well suited to automotive, communications, and other applications.

  15. High-temperature compatibility between liquid metal as PWR fuel gap filler and stainless steel and high-density concrete

    Science.gov (United States)

    Wongsawaeng, Doonyapong; Jumpee, Chayanit; Jitpukdee, Manit

    2014-08-01

    In conventional nuclear fuel rods for light-water reactors, a helium-filled as-fabricated gap between the fuel and the cladding inner surface accommodates fuel swelling and cladding creep down. Because helium exhibits a very low thermal conductivity, it results in a large temperature rise in the gap. Liquid metal (LM; 1/3 weight portion each of lead, tin, and bismuth) has been proposed to be a gap filler because of its high thermal conductivity (∼100 times that of He), low melting point (∼100 °C), and lack of chemical reactivity with UO2 and water. With the presence of LM, the temperature drop across the gap is virtually eliminated and the fuel is operated at a lower temperature at the same power output, resulting in safer fuel, delayed fission gas release and prevention of massive secondary hydriding. During normal reactor operation, should an LM-bonded fuel rod failure occurs resulting in a discharge of liquid metal into the bottom of the reactor pressure vessel, it should not corrode stainless steel. An experiment was conducted to confirm that at 315 °C, LM in contact with 304 stainless steel in the PWR water chemistry environment for up to 30 days resulted in no observable corrosion. Moreover, during a hypothetical core-melt accident assuming that the liquid metal with elevated temperature between 1000 and 1600 °C is spread on a high-density concrete basement of the power plant, a small-scale experiment was performed to demonstrate that the LM-concrete interaction at 1000 °C for as long as 12 h resulted in no penetration. At 1200 °C for 5 h, the LM penetrated a distance of ∼1.3 cm, but the penetration appeared to stop. At 1400 °C the penetration rate was ∼0.7 cm/h. At 1600 °C, the penetration rate was ∼17 cm/h. No corrosion based on chemical reactions with high-density concrete occurred, and, hence, the only physical interaction between high-temperature LM and high-density concrete was from tiny cracks generated from thermal stress. Moreover

  16. Reserve, flowing electrolyte, high rate lithium battery

    Science.gov (United States)

    Puskar, M.; Harris, P.

    Flowing electrolyte Li/SOCl2 tests in single cell and multicell bipolar fixtures have been conducted, and measurements are presented for electrolyte flow rates, inlet and outlet temperatures, fixture temperatures at several points, and the pressure drop across the fixture. Reserve lithium batteries with flowing thionyl-chloride electrolytes are found to be capable of very high energy densities with usable voltages and capacities at current densities as high as 500 mA/sq cm. At this current density, a battery stack 10 inches in diameter is shown to produce over 60 kW of power while maintaining a safe operating temperature.

  17. A Cooperative Interface for Highly Efficient Lithium-Sulfur Batteries.

    Science.gov (United States)

    Peng, Hong-Jie; Zhang, Ze-Wen; Huang, Jia-Qi; Zhang, Ge; Xie, Jin; Xu, Wen-Tao; Shi, Jia-Le; Chen, Xiang; Cheng, Xin-Bing; Zhang, Qiang

    2016-11-01

    A cooperative interface constructed by "lithiophilic" nitrogen-doped graphene frameworks and "sulfiphilic" nickel-iron layered double hydroxides (LDH@NG) is proposed to synergistically afford bifunctional Li and S binding to polysulfides, suppression of polysulfide shuttles, and electrocatalytic activity toward formation of lithium sulfides for high-performance lithium-sulfur batteries. LDH@NG enables high rate capability, long lifespan, and efficient stabilization of both sulfur and lithium electrodes.

  18. Lithium

    Science.gov (United States)

    Jaskula, B.W.

    2012-01-01

    In 2011, world lithium consumption was estimated to have been about 25 kt (25,000 st) of lithium contained in minerals and compounds, a 10-percent increase from 2010. U.S. consumption was estimated to have been about 2 kt (2,200 st) of contained lithium, a 100-percent increase from 2010. The United States was estimated to be the fourth-ranked consumer of lithium and remained the leading importer of lithium carbonate and the leading producer of value-added lithium materials. One company, Chemetall Foote Corp. (a subsidiary of Chemetall GmbH of Germany), produced lithium compounds from domestic brine resources near Silver Peak, NV.

  19. Novel High Rate Lithium Intercalation Cathode Materials

    Institute of Scientific and Technical Information of China (English)

    2005-01-01

    Application of amorphous V2O5/carbon/neodymium oxide (Nd2O3) composite is one of ways to surmount the lower electrical conductivity of V2O5. A new type of V2O5/carbon/Nd2O3 composite was prepared by mixing vanadium oxide hydrosol, acetone, carbon and Nd2O3 powder. High rate discharge/charge property of the composite electrode was tested electrochemically. This composite with Nd2O3 added shows the improvement of not only the discharge capacity but also cycle durability discharge capacity. The rate capability of the composite cathode also increases with the addition of Nd2O3.and cycle life are probably caused by the increase in porosity of open pores and short diffusion length of the active material on the lithium-ion insertion.

  20. High capacity anode materials for lithium ion batteries

    Energy Technology Data Exchange (ETDEWEB)

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

    2015-11-19

    High capacity silicon based anode active materials are described for lithium ion batteries. These materials are shown to be effective in combination with high capacity lithium rich cathode active materials. Supplemental lithium is shown to improve the cycling performance and reduce irreversible capacity loss for at least certain silicon based active materials. In particular silicon based active materials can be formed in composites with electrically conductive coatings, such as pyrolytic carbon coatings or metal coatings, and composites can also be formed with other electrically conductive carbon components, such as carbon nanofibers and carbon nanoparticles. Additional alloys with silicon are explored.

  1. Experiment on the improvement of sinterability for dry recycling nuclear fuel pellets by using simulated spent PWR fuel of high burnup

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Woong Ki; Kim, S. S.; Park, G. I.; Lee, Jae W.; Cho, K. H.; Lee, D. Y.; Lee, Y. S.; Lee, J. W.; Yang, M. S.; Shin, W. C

    2004-09-01

    To study the fabrication characteristics of dry recycling nuclear fuel using spent PWR fuel with high burnup of 60,000 MWd/tU, the fission products of spent PWR fuel was analyzed by ORIGEN-2 code. Simulated spent PWR fuel pellets were fabricated by using UO{sub 2} powder added by the simulated fission products. The simulated dry-recycling-fuel pellets were fabricated by dry recycling fuel fabrication flow including 3 cycle treated OREOX(Oxidation and REduction of OXide fuel) process. A small amount of dopant such as TiO{sub 2}, Nb{sub 2}O{sub 5}, Li{sub 2}O are added to increase sinterability of the OREOX treated powder. As the results of experiments, the densities of sintered pellets without dopant ranged from 10.04 to 10.34 g/cm{sup 3}(94.3 to 97.1% of T.D.), the grain size of the pellets ranged from 3 to 4 {mu}m. The sintered density of the pellets with TiO{sub 2} or Nb{sub 2}O{sub 5} ranged from 10.46 to 10.32 g/cm{sup 3}(98.2 to 96.9 % of T.D.) The grain size of the pellets with TiO{sub 2}, Nb{sub 2}O{sub 5} or Li{sub 2}O ranged from 7.3 to 12.2 {mu}m.

  2. High Energy Density Battery Lithium Thionyl Chloride Improved Reverse Voltage Design.

    Science.gov (United States)

    1981-12-01

    BATTERY LITHIUM THIONYL CHLORIDE IMPROVED R-ETC(U) DEC 81 A E ZOLLA N660011-C-0310...HIGH ENERGY DENSITY BATTERY LITHIUM THIONYL CHLORIDE IMPROVED REVERSE VOLTAGE DESIGN Dr. A. E. Zolla Altus Corporation C:1 1610 Crane Court San Jose...reverse aide If necesary and identify by block number) Lithium Battery Lithium Thionyl Chloride High Energy Density Battery Voltage Reversal Battery

  3. Lithium

    Science.gov (United States)

    Lithium is used to treat and prevent episodes of mania (frenzied, abnormally excited mood) in people with bipolar disorder (manic-depressive disorder; a disease that causes episodes of depression, episodes of mania, and other abnormal ...

  4. Development of novel cathodes for high energy density lithium batteries

    Science.gov (United States)

    Bhargav, Amruth

    Lithium based batteries have become ubiquitous with our everyday life. They have propelled a generation of smart personal electronics and electric transport. Their use is now percolating to various fields as a source of energy to facilitate the operation of devices from nanoscale to mega scale. This need for a portable energy source has led to tremendous scientific interest in this field to develop electrochemical devices like batteries with higher capacities, longer cycle life and increased safety at a low cost. To this end, the research presented in this thesis focuses on two emerging and promising technologies called lithium-oxygen (Li-O2) and lithium-sulfur (Li-S) batteries. These batteries can offer an order of magnitude higher capacities through cheap, environmentally safe and abundant elements namely oxygen and sulfur. The first work introduces the concept of closed system lithium-oxygen batteries wherein the cell contains the discharge product of Li-O2 batteries namely, lithium peroxide (Li2O2) as the starting active material. The reversibility of this system is analyzed along with its rate performance. The possible use of such a cathode in a full cell is explored. Also, this concept is used to verify if all the lithium can be extracted from the cathode in the first charge. In the following work, lithium peroxide is chemically synthesized and deposited in a carbon nanofiber matrix. This forms a free standing cathode that shows high reversibility. It can be cycled up to 20 times and while using capacity control protocol, a cycle life of 50 is obtained. The cause of cell degradation and failure is also analyzed. In the work on full cell lithium-sulfur system, a novel electrolyte is developed that can support reversible lithium insertion and extraction from a graphite anode. A method to deposit solid lithium polysulfide is developed for the cathode. Coupling a lithiated graphite anode with the cathode using the new electrolyte yields a full cell whose

  5. Liquid lithium for high power density fragmentation targets

    Science.gov (United States)

    Nolen, J. A.; Reed, C. B.; Hassanein, A.; Morrissey, D. J.; Ottarson, J. H.; Sherrill, B. M.

    2001-10-01

    Windowless liquid lithium targets for in-flight fragmentation or fission of high power heavy ion beams are being developed for the U.S. RIA project. With uranium beam power of 100 kW and a beam spot diameter of 1 mm the power density in the target is over 1 MW/cm3. Thermal analysis for this example indicates a very low peak temperature for the lithium when flowing at a linear velocity of 10 m/s. A vacuum test chamber is under construction at Argonne at an existing liquid lithium facility to demonstrate a 2 cm thick windowless target. As a first step towards using liquid lithium target technology at a nuclear physics fragmentation facility, a lower power target is being constructed for use at the NSCL. This target will use beryllium windows with flowing lithium. It is designed for beams between oxygen and calcium with beam power above 3 kW. The tapered beryllium windows are each 1 mm thick for the calcium beams and 7 mm thick for the oxygen beams. The lithium is 5 mm thick. This gives an overall target thickness ranging from about 1 g/cm2 to 3 g/cm2 which is adjusted by moving the target vertically. The designs of these targets and the status of the prototypes will be discussed.

  6. High-discharge-rate lithium ion battery

    Science.gov (United States)

    Liu, Gao; Battaglia, Vincent S; Zheng, Honghe

    2014-04-22

    The present invention provides for a lithium ion battery and process for creating such, comprising higher binder to carbon conductor ratios than presently used in the industry. The battery is characterized by much lower interfacial resistances at the anode and cathode as a result of initially mixing a carbon conductor with a binder, then with the active material. Further improvements in cycleability can also be realized by first mixing the carbon conductor with the active material first and then adding the binder.

  7. Graphical and tabular summaries of decay characteristics for once-through PWR, LMFBR, and FFTF fuel cycle materials. [Spent fuel, high-level waste fuel can scrap

    Energy Technology Data Exchange (ETDEWEB)

    Croff, A.G.; Liberman, M.S.; Morrison, G.W.

    1982-01-01

    Based on the results of ORIGEN2 and a newly developed code called ORMANG, graphical and summary tabular characteristics of spent fuel, high-level waste, and fuel assembly structural material (cladding) waste are presented for a generic pressurized-water reactor (PWR), a liquid-metal fast breeder reactor (LMFBR), and the Fast Flux Test Facility (FFTF). The characteristics include radioactivity, thermal power, and toxicity (water dilution volume). Given are graphs and summary tables containing characteristic totals and the principal nuclide contributors as well as graphs comparing the three reactors for a single material and the three materials for a single reactor.

  8. Recycling rice husks for high-capacity lithium battery anodes.

    Science.gov (United States)

    Jung, Dae Soo; Ryou, Myung-Hyun; Sung, Yong Joo; Park, Seung Bin; Choi, Jang Wook

    2013-07-23

    The rice husk is the outer covering of a rice kernel and protects the inner ingredients from external attack by insects and bacteria. To perform this function while ventilating air and moisture, rice plants have developed unique nanoporous silica layers in their husks through years of natural evolution. Despite the massive amount of annual production near 10(8) tons worldwide, so far rice husks have been recycled only for low-value agricultural items. In an effort to recycle rice husks for high-value applications, we convert the silica to silicon and use it for high-capacity lithium battery anodes. Taking advantage of the interconnected nanoporous structure naturally existing in rice husks, the converted silicon exhibits excellent electrochemical performance as a lithium battery anode, suggesting that rice husks can be a massive resource for use in high-capacity lithium battery negative electrodes.

  9. An improved high-performance lithium-air battery

    Science.gov (United States)

    Jung, Hun-Gi; Hassoun, Jusef; Park, Jin-Bum; Sun, Yang-Kook; Scrosati, Bruno

    2012-07-01

    Although dominating the consumer electronics markets as the power source of choice for popular portable devices, the common lithium battery is not yet suited for use in sustainable electrified road transport. The development of advanced, higher-energy lithium batteries is essential in the rapid establishment of the electric car market. Owing to its exceptionally high energy potentiality, the lithium-air battery is a very appealing candidate for fulfilling this role. However, the performance of such batteries has been limited to only a few charge-discharge cycles with low rate capability. Here, by choosing a suitable stable electrolyte and appropriate cell design, we demonstrate a lithium-air battery capable of operating over many cycles with capacity and rate values as high as 5,000 mAh gcarbon-1 and 3 A gcarbon-1, respectively. For this battery we estimate an energy density value that is much higher than those offered by the currently available lithium-ion battery technology.

  10. Hydrogen, lithium, and lithium hydride production

    Science.gov (United States)

    Brown, Sam W; Spencer, Larry S; Phillips, Michael R; Powell, G. Louis; Campbell, Peggy J

    2014-03-25

    A method of producing high purity lithium metal is provided, where gaseous-phase lithium metal is extracted from lithium hydride and condensed to form solid high purity lithium metal. The high purity lithium metal may be hydrided to provide high purity lithium hydride.

  11. A High Fidelity Multiphysics Framework for Modeling CRUD Deposition on PWR Fuel Rods

    Science.gov (United States)

    Walter, Daniel John

    Corrosion products on the fuel cladding surfaces within pressurized water reactor fuel assemblies have had a significant impact on reactor operation. These types of deposits are referred to as CRUD and can lead to power shifts, as a consequence of the accumulation of solid boron phases on the fuel rod surfaces. Corrosion deposits can also lead to fuel failure resulting from localized corrosion, where the increased thermal resistance of the deposit leads to higher cladding temperatures. The prediction of these occurrences requires a comprehensive model of local thermal hydraulic and chemical processes occurring in close proximity to the cladding surface, as well as their driving factors. Such factors include the rod power distribution, coolant corrosion product concentration, as well as the feedbacks between heat transfer, fluid dynamics, chemistry, and neutronics. To correctly capture the coupled physics and corresponding feedbacks, a high fidelity framework is developed that predicts three-dimensional CRUD deposition on a rod-by-rod basis. Multiphysics boundary conditions resulting from the coupling of heat transfer, fluid dynamics, coolant chemistry, CRUD deposition, neutron transport, and nuclide transmutation inform the CRUD deposition solver. Through systematic parametric sensitivity studies of the CRUD property inputs, coupled boundary conditions, and multiphysics feedback mechanisms, the most important variables of multiphysics CRUD modeling are identified. Moreover, the modeling framework is challenged with a blind comparison of plant data to predictions by a simulation of a sub-assembly within the Seabrook nuclear plant that experienced CRUD induced fuel failures. The physics within the computational framework are loosely coupled via an operator-splitting technique. A control theory approach is adopted to determine the temporal discretization at which to execute a data transfer from one physics to another. The coupled stepsize selection is viewed as a

  12. Analysis of Experimental Data for High Burnup PWR Spent Fuel Isotopic Validation - Vandellos II Reactor

    Energy Technology Data Exchange (ETDEWEB)

    Ilas, Germina [ORNL; Gauld, Ian C [ORNL

    2011-01-01

    This report is one of the several recent NUREG/CR reports documenting benchmark-quality radiochemical assay data and the use of the data to validate computer code predictions of isotopic composition for spent nuclear fuel, to establish the uncertainty and bias associated with code predictions. The experimental data analyzed in the current report were acquired from a high-burnup fuel program coordinated by Spanish organizations. The measurements included extensive actinide and fission product data of importance to spent fuel safety applications, including burnup credit, decay heat, and radiation source terms. Six unique spent fuel samples from three uranium oxide fuel rods were analyzed. The fuel rods had a 4.5 wt % {sup 235}U initial enrichment and were irradiated in the Vandellos II pressurized water reactor operated in Spain. The burnups of the fuel samples range from 42 to 78 GWd/MTU. The measurements were used to validate the two-dimensional depletion sequence TRITON in the SCALE computer code system.

  13. High power density self-cooled lithium-vanadium blanket.

    Energy Technology Data Exchange (ETDEWEB)

    Gohar, Y.; Majumdar, S.; Smith, D.

    1999-07-01

    A self-cooled lithium-vanadium blanket concept capable of operating with 2 MW/m{sup 2} surface heat flux and 10 MW/m{sup 2} neutron wall loading has been developed. The blanket has liquid lithium as the tritium breeder and the coolant to alleviate issues of coolant breeder compatibility and reactivity. Vanadium alloy (V-4Cr-4Ti) is used as the structural material because it can accommodate high heat loads. Also, it has good mechanical properties at high temperatures, high neutron fluence capability, low degradation under neutron irradiation, good compatibility with the blanket materials, low decay heat, low waste disposal rating, and adequate strength to accommodate the electromagnetic loads during plasma disruption events. Self-healing electrical insulator (CaO) is utilized to reduce the MHD pressure drop. A poloidal coolant flow with high velocity at the first wall is used to reduce the peak temperature of the vanadium structure and to accommodate high surface heat flux. The blanket has a simple blanket configuration and low coolant pressure to reduce the fabrication cost, to improve the blanket reliability, and to increase confidence in the blanket performance. Spectral shifter, moderator, and reflector are utilized to improve the blanket shielding capability and energy multiplication, and to reduce the radial blanket thickness. Natural lithium is used to avoid extra cost related to the lithium enrichment process.

  14. High power density self-cooled lithium-vanadium blanket.

    Energy Technology Data Exchange (ETDEWEB)

    Gohar, Y.; Majumdar, S.; Smith, D.

    1999-07-01

    A self-cooled lithium-vanadium blanket concept capable of operating with 2 MW/m{sup 2} surface heat flux and 10 MW/m{sup 2} neutron wall loading has been developed. The blanket has liquid lithium as the tritium breeder and the coolant to alleviate issues of coolant breeder compatibility and reactivity. Vanadium alloy (V-4Cr-4Ti) is used as the structural material because it can accommodate high heat loads. Also, it has good mechanical properties at high temperatures, high neutron fluence capability, low degradation under neutron irradiation, good compatibility with the blanket materials, low decay heat, low waste disposal rating, and adequate strength to accommodate the electromagnetic loads during plasma disruption events. Self-healing electrical insulator (CaO) is utilized to reduce the MHD pressure drop. A poloidal coolant flow with high velocity at the first wall is used to reduce the peak temperature of the vanadium structure and to accommodate high surface heat flux. The blanket has a simple blanket configuration and low coolant pressure to reduce the fabrication cost, to improve the blanket reliability, and to increase confidence in the blanket performance. Spectral shifter, moderator, and reflector are utilized to improve the blanket shielding capability and energy multiplication, and to reduce the radial blanket thickness. Natural lithium is used to avoid extra cost related to the lithium enrichment process.

  15. High performance discharges in the Lithium Tokamak eXperiment with liquid lithium wallsa)

    Science.gov (United States)

    Schmitt, J. C.; Bell, R. E.; Boyle, D. P.; Esposti, B.; Kaita, R.; Kozub, T.; LeBlanc, B. P.; Lucia, M.; Maingi, R.; Majeski, R.; Merino, E.; Punjabi-Vinoth, S.; Tchilingurian, G.; Capece, A.; Koel, B.; Roszell, J.; Biewer, T. M.; Gray, T. K.; Kubota, S.; Beiersdorfer, P.; Widmann, K.; Tritz, K.

    2015-05-01

    The first-ever successful operation of a tokamak with a large area (40% of the total plasma surface area) liquid lithium wall has been achieved in the Lithium Tokamak eXperiment (LTX). These results were obtained with a new, electron beam-based lithium evaporation system, which can deposit a lithium coating on the limiting wall of LTX in a five-minute period. Preliminary analyses of diamagnetic and other data for discharges operated with a liquid lithium wall indicate that confinement times increased by 10× compared to discharges with helium-dispersed solid lithium coatings. Ohmic energy confinement times with fresh lithium walls, solid and liquid, exceed several relevant empirical scaling expressions. Spectroscopic analysis of the discharges indicates that oxygen levels in the discharges limited on liquid lithium walls were significantly reduced compared to discharges limited on solid lithium walls. Tokamak operations with a full liquid lithium wall (85% of the total plasma surface area) have recently started.

  16. High-capacity nanocarbon anodes for lithium-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Haitao; Sun, Xianzhong; Zhang, Xiong; Lin, He; Wang, Kai; Ma, Yanwei, E-mail: ywma@mail.iee.ac.cn

    2015-02-15

    Highlights: • The nanocarbon anodes in lithium-ion batteries deliver a high capacity of ∼1100 mA h g{sup −1}. • The nanocarbon anodes exhibit excellent cyclic stability. • A novel structure of carbon materials, hollow carbon nanoboxes, has potential application in lithium-ion batteries. - Abstract: High energy and power density of secondary cells like lithium-ion batteries become much more important in today’s society. However, lithium-ion battery anodes based on graphite material have theoretical capacity of 372 mA h g{sup −1} and low charging-discharging rate. Here, we report that nanocarbons including mesoporous graphene (MPG), carbon tubular nanostructures (CTN), and hollow carbon nanoboxes (HCB) are good candidate for lithium-ion battery anodes. The nanocarbon anodes have high capacity of ∼1100, ∼600, and ∼500 mA h g{sup −1} at 0.1 A g{sup −1} for MPG, CTN, and HCB, respectively. The capacity of 181, 141, and 139 mA h g{sup −1} at 4 A g{sup −1} for MPG, CTN, and HCB anodes is retained. Besides, nanocarbon anodes show high cycling stability during 1000 cycles, indicating formation of a passivating layer—solid electrolyte interphase, which support long-term cycling. Nanocarbons, constructed with graphene layers which fulfill lithiation/delithiation process, high ratio of graphite edge structure, and high surface area which facilitates capacitive behavior, deliver high capacity and improved rate-capability.

  17. Study for highly functional resin (macroporous resin) superior in removing micro particles in PWR primary circuit: on-site test

    Energy Technology Data Exchange (ETDEWEB)

    Itou, A.; Kondo, K.; Kouzuma, Y., E-mail: ayumu_itou@kyuden.co.jp [Kyusyu Electric Power Co., Inc., Minami-ku, Fukuoka (Japan); Umehara, R.; Shimizu, Y., E-mail: Ruyji_Umehara@mhi.co.jp [Mitsubishi Heavy Industries, Ltd., Hyogo-ku, Kobe (Japan); Kogawa, N.; Nagamine, K., E-mail: nkogawa@ndc.hq.mhi.co.jp [Nuclear Development Corp., Tokaimura, Ibaraki (Japan)

    2010-07-01

    In Japanese PWR plants, efforts to remove particulate constituents containing radioactive cobalt which provides a source of radiation exposure, are needed. Performance evaluation study was conducted for macroporous resin which was said to possess excellent performance in removing particulate constituents and whose practical accomplishment at plants in USA was reported to be good. As one of the means for radiation exposure reduction in PWR, a study for application of crud removing resin to actual plant was executed by laboratory experiments using simulated crud (Fe{sub 3}O{sub 4} particle). In this study, following two mechanisms were demonstrated as the particle capturing mechanism of macroporous resin; physical trapping by fine pores on resin surface; electrical adsorption onto resin surface. In addition, in parallel to the study for application of macroporous resin to actual PWR plant, on-site study was planned to investigate the primary system water chemistry during various stages of actual plant operation and to research performance of particle capturing in detail. As the on-site study, column experiments, there water was let pass through the column, were planned for various operation stage (startup period, power operation period and shutdown period). A kind of conventional gel-type resin and three kinds of macroporous resin were examined for onsite tests. As to particulate capturing, basic knowledge regarding capturing efficiency and influence of water chemistry on capturing performance were ordered. Capturing performance of each resin tested became clear and was ordered by comparison. Effectiveness of macroporous resin with regard to crud removal in primary coolant was confirmed. (author)

  18. In-situ oxide layer analysis of alloy 182 using electrochemical impedance spectroscopy in high dissolved hydrogen condition in PWR environment

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Ho-Sub; Subramanian, Gokul Obulan; Hong, Jong-Dae; Lee, Junho; Jang, Changheui [KAIST, Daejeon (Korea, Republic of)

    2015-05-15

    Alloy 82/182 weld metals had been extensively used in joining the components of the PWR primary system. Unfortunately, the cracking caused by PWSCC usually occurs on Alloy 82/182 dissimilar metal welds (DMW). Previous studies indicated that the susceptibility of PWSCC is closely related to the oxide characteristics which are dependent on water chemistry condition, especially dissolved hydrogen (DH). Furthermore, in primary system of pressurized water reactor (PWR), crack initiation resulted from electrochemical instability of oxide film of Ni-base structural materials in various hydrogen concentrations. In this study, in-situ oxide analysis of Alloy 182 using electrochemical impedance spectroscopy (EIS) was performed in high dissolved hydrogen condition. Especially, to understand the effects of tensile loading on the oxide characteristics, we tried to characterize the oxides formed on the tensile loaded specimen using in-situ EIS analysis. The EIS analysis of oxide on Alloy 182 was performed. The increase of oxide film thickness was observed with the increase of exposure time. To analysis the multi-layer structure of oxides, an equivalent model was obtained by fitting EIS data. It is assumed that overall oxide structures were composed of 3 layers approximately.

  19. Nano-Composite Cathodes for High Performance Lithium Ion Microbatteries Project

    Data.gov (United States)

    National Aeronautics and Space Administration — TPL Inc. proposes to develop a novel, high performance, nanostructured cathode material for lithium ion (Li-ion) batteries. The proposed approach will modify lithium...

  20. Standard PWR for Italy

    Energy Technology Data Exchange (ETDEWEB)

    Negroni, A.; Velona, F. (Ente Nazionale per l' Energia Elettrica, Rome (Italy))

    1983-03-01

    A description is given of the general design for the standard PWR which will be used in the seven to eight nuclear power stations provided for in the Italian national energy plan. Special features to meet Italian conditions include double containment and a common foundation mat for the reactor, auxiliary and fuel buildings.

  1. Lithium manganese spinel materials for high-rate electrochemical applications

    Institute of Scientific and Technical Information of China (English)

    Anna V. Potapenko; Sviatoslav A. Kirillov

    2014-01-01

    In order to successively compete with supercapacitors, an ability of fast discharge is a must for lithium-ion batteries. From this point of view, stoichiometric and substituted lithium manganese spinels as cathode materials are one of the most prospective candidates, especially in their nanosized form. In this article, an overview of the most recent data regarding physico-chemical and electrochemical properties of lithium manganese spinels, especially, LiMn2O4 and LiNi0.5Mn1.5O4, synthesized by means of various methods is presented, with special emphasis of their use in high-rate electrochemical applications. In particular, specific capacities and rate capabilities of spinel materials are analyzed. It is suggested that reduced specific capacity is determined primarily by the aggregation of material particles, whereas good high-rate capability is governed not only by the size of crystallites but also by the perfectness of crystals. The most technologically advantageous solutions are described, existing gaps in the knowledge of spinel materials are outlined, and the ways of their filling are suggested, in a hope to be helpful in keeping lithium batteries afloat in the struggle for a worthy place among electrochemical energy systems of the 21st century.

  2. High-throughput theoretical design of lithium battery materials

    Science.gov (United States)

    Shi-Gang, Ling; Jian, Gao; Rui-Juan, Xiao; Li-Quan, Chen

    2016-01-01

    The rapid evolution of high-throughput theoretical design schemes to discover new lithium battery materials is reviewed, including high-capacity cathodes, low-strain cathodes, anodes, solid state electrolytes, and electrolyte additives. With the development of efficient theoretical methods and inexpensive computers, high-throughput theoretical calculations have played an increasingly important role in the discovery of new materials. With the help of automatic simulation flow, many types of materials can be screened, optimized and designed from a structural database according to specific search criteria. In advanced cell technology, new materials for next generation lithium batteries are of great significance to achieve performance, and some representative criteria are: higher energy density, better safety, and faster charge/discharge speed. Project supported by the National Natural Science Foundation of China (Grant Nos. 11234013 and 51172274) and the National High Technology Research and Development Program of China (Grant No. 2015AA034201).

  3. High rate lithium/thionyl chloride bipolar battery development

    Energy Technology Data Exchange (ETDEWEB)

    Russell, P.G. [Yardney Technical Products, Inc., Pawcatuck, CT (United States); Goebel, F. [Yardney Technical Products, Inc., Pawcatuck, CT (United States)

    1995-04-01

    The lithium/thionyl chloride (Li/SOCl{sub 2}) electrochemistry is capable of providing high power and high specific power, especially under pulse discharge conditions, when cells containing thin components are arranged in a bipolar configuration. This paper describes recent work concerned with bipolar cell design, cathode evaluation, component manufacturing methods, and the assembly and testing of bipolar modules containing up to 150 cells for Sonobuoy application. (orig.)

  4. High rate lithium-thionyl chloride bipolar battery development

    Energy Technology Data Exchange (ETDEWEB)

    Russell, P.G.; Goebel, F. [Yardney Technical Products, Inc., Pawcatuck, CT (United States)

    1994-12-31

    The lithium/thionyl chloride system is capable of providing both high power and high energy density when cells containing thin components are arranged in a bipolar configuration. Electrode current densities in excess of 300mA/cm{sup 2} are achieved during pulse discharge. The present work is concerned with bipolar cell design, cathode evaluation, component manufacturing methods, and the assembly and testing of bipolar modules containing up to 150 cells.

  5. High rate lithium/thionyl chloride bipolar battery development

    Science.gov (United States)

    Russell, P. G.; Goebel, F.

    The lithium/thionyl chloride ( {Li}/{SOCl2}) electrochemistry is capable of providing high power and high specific power, especially under pulse discharge conditions, when cells containing thin components are arranged in a bipolar configuration. This paper describes recent work concerned with bipolar cell design, cathode evaluation, component manufacturing methods, and the assembly and testing of bipolar modules containing up to 150 cells for Sonobuoy application.

  6. Open and closed fuel cycle of HWR and PWR. How large is the high-level radioactive wastes repository; Ciclos de combustible abierto y cerrado con HWR y PWR. ?Cuanto mas grande es el repositorio de residuos radiactivos de alta actividad?

    Energy Technology Data Exchange (ETDEWEB)

    Bevilacqua, Arturo M. [Comision Nacional de Energia Atomica, San Carlos de Bariloche (Argentina). Centro Atomico Bariloche

    1996-07-01

    A conceptual analysis was carried out on the size of a high-level wastes (HLW) repository for the waste arising from once-through and closed fuel cycles with (HLW) and PWR. The mass, the activity and thermal loading was calculated with the ORIGEN2.1 computer code for the spent fuel and for the high-level liquid wastes. It was considered a minimum burnup of 7.000 MW.d/t U and 33.000 MW.d/t U for HWR and PWR respectively, cooling times of 20 and 55 years, reprocessing recovery ratios of 99% and 99.7% and a total electricity production of 81.6 GW(e).a. It was concluded that the cooling time is the most important repository size reproduction parameter for the closed cycles. On the other hand, the spent fuel mass for the once-through cycles does not depend on the cooling time what prevents repository size reduction once a cooling time of 55 years is reached. The repository size reduction in the case of HWR is larger than in the case of PWR, owing to the larger fuel mass required to produce the specific electricity amount. (author)

  7. Outcome of lithium prophylaxis: a prospective follow-up of affective disorder patients assigned to high and low serum lithium levels

    DEFF Research Database (Denmark)

    Vestergaard, Per; Licht, Rasmus Wentzer; Brodersen, Anders Torp

    1998-01-01

    The purpose of the study was to examine the outcome of long-term lithium treatment in consecutively admitted affective disorder patients assigned to high and low serum lithium levels. A total of 91 patients were diagnosed according to DSM-III criteria and randomly allocated to two open treatment...... on lithium, and 42 patients (46%) discontinued lithium or were lost to follow-up. No effect of treatment group was seen, either for the total patient group or for the large subgroup of bipolar patients when analysed separately. A number of patients did not maintain their original assignment to the high serum...... groups in which prophylactic lithium was administered in high (serum lithium 0.8-1.0 mmol L-1) and low (serum lithium 0.5-0.8 mmol L-1) doses, respectively. The patients were followed for 2 years or until discontinuation of lithium treatment or readmission to hospital for recurrence of affective illness...

  8. Benefits of Nanostructuring Electrodes for High-Energy and High-Power Lithium Batteries

    Institute of Scientific and Technical Information of China (English)

    Joachim; Maier

    2007-01-01

    1 Results One of the greatest challenges for our society is providing powerful electrochemical energy storage devices with both high energy and high power densities. Rechargeable lithium-based batteries are amongst the most promising candidates in terms of energy density,the achievement of high power density is hindered by kinetic problems of the electrode materials.This contribution that emphasizes the power of nanostructuring for electrodes in lithium-based batteries,deals with several nanostructured ...

  9. Utilization of spent PWR fuel-advanced nuclear fuel cycle of PWR/CANDU synergism

    Institute of Scientific and Technical Information of China (English)

    HUO Xiao-Dong; XIE Zhong-Sheng

    2004-01-01

    High neutron economy, on line refueling and channel design result in the unsurpassed fuel cycle flexibility and variety for CANDU reactors. According to the Chinese national conditions that China has both PWR and CANDU reactors and the closed cycle policy of reprocessing the spent PWR fuel is adopted, one of the advanced nuclear fuel cycles of PWR/CANDU synergism using the reprocessed uranium of spent PWR fuel in CANDU reactor is proposed, which will save the uranium resource (~22.5%), increase the energy output (~41%), decrease the quantity of spent fuels to be disposed (~2/3) and lower the cost of nuclear power. Because of the inherent flexibility of nuclear fuel cycle in CANDU reactor, and the low radiation level of recycled uranium(RU), which is acceptable for CANDU reactor fuel fabrication, the transition from the natural uranium to the RU can be completed without major modification of the reactor core structure and operation mode. It can be implemented in Qinshan Phase Ⅲ CANDU reactors with little or no requirement of big investment in new design. It can be expected that the reuse of recycled uranium of spent PWR fuel in CANDU reactor is a feasible and desirable strategy in China.

  10. Abuse behavior of high-power, lithium-ion cells

    Science.gov (United States)

    Spotnitz, R.; Franklin, J.

    Published accounts of abuse testing of lithium-ion cells and components are summarized, including modeling work. From this summary, a set of exothermic reactions is selected with corresponding estimates of heats of reaction. Using this set of reactions, along with estimated kinetic parameters and designs for high-rate batteries, models for the abuse behavior (oven, short-circuit, overcharge, nail, crush) are developed. Finally, the models are used to determine that fluorinated binder plays a relatively unimportant role in thermal runaway.

  11. Polyimide encapsulated lithium-rich cathode material for high voltage lithium-ion battery.

    Science.gov (United States)

    Zhang, Jie; Lu, Qingwen; Fang, Jianhua; Wang, Jiulin; Yang, Jun; NuLi, Yanna

    2014-10-22

    Lithium-rich materials represented by xLi2MnO3·(1 - x)LiMO2 (M = Mn, Co, Ni) are attractive cathode materials for lithium-ion battery due to their high specific energy and low cost. However, some drawbacks of these materials such as poor cycle and rate capability remain to be addressed before applications. In this study, a thin polyimide (PI) layer is coated on the surface of Li1.2Ni0.13Mn0.54Co0.13O2 (LNMCO) by a polyamic acid (PAA) precursor with subsequently thermal imidization process. X-ray diffraction (XRD), scanning electron microscopy (SEM), and high-resolution transmission electron microscopy (HR-TEM) results confirm the successful formation of a PI layer (∼3 nm) on the surface of LNMCO without destruction of its main structure. X-ray photoelectron spectroscopy (XPS) spectra show a slight shift of the Mn valence state from Mn(IV) to Mn(III) in the PI-LNMCO treated at 450 °C, elucidating that charge transfer takes place between the PI layer and LNMCO surface. Electrochemical performances of LNMCO including cyclic stability and rate capability are evidently improved by coating a PI nanolayer, which effectively separates the cathode material from the electrolyte and stabilizes their interface at high voltage.

  12. High conducting oxide--sulfide composite lithium superionic conductor

    Energy Technology Data Exchange (ETDEWEB)

    Liang, Chengdu; Rangasamy, Ezhiylmurugan; Dudney, Nancy J.; Keum, Jong Kahk; Rondinone, Adam Justin

    2017-01-17

    A solid electrolyte for a lithium-sulfur battery includes particles of a lithium ion conducting oxide composition embedded within a lithium ion conducting sulfide composition. The lithium ion conducting oxide composition can be Li.sub.7La.sub.3Zr.sub.2O.sub.12 (LLZO). The lithium ion conducting sulfide composition can be .beta.-Li.sub.3PS.sub.4 (LPS). A lithium ion battery and a method of making a solid electrolyte for a lithium ion battery are also disclosed.

  13. [Treatment of acute lithium intoxication with high-flux haemodialysis membranes].

    Science.gov (United States)

    Peces, R; Fernández, E J; Regidor, D; Peces, C; Sánchez, R; Montero, A; Selgas, R

    2006-01-01

    Lithium carbonate is commonly prescribed for the treatment of bipolar (manic-depressive) disorders. However, because of its narrow therapeutic index an excessive elevation of serum lithium concentration, either during chronic maintenance therapy or after an acute overdose, can result in serious toxicity. In addition to supportive care, the established treatment of severe lithium toxicity is haemodialysis. Conventional haemodialysis can reduce serum lithium rapidly, but post-dialysis rebound elevations with recurrent toxicity have been documented in old publications. High-flux membranes should be capable of removing more lithium per hour of haemodialysis, but published values are not available. We report here three patients with acute lithium intoxication who were treated successfully with bicarbonate and high-flux haemodialysis membranes. Our patients presented with a severe degree of intoxication, based on the amount of drug ingested, the initial serum lithium level, the severity of neurologic symptoms and systemic manifestations. Two patients developed acute renal failure probably as a result of volume depletion since it was rapidly reversible by haemodialysis and infusion therapy. In addition, consecutive haemodialysis sessions and improvement of renal function allowed a rapid decrease in serum lithium levels without haemodynamic instability or rebound elevations in lithium concentration. The effectiveness of the procedure in these cases can be attributed to the use of bicarbonate dialysate and high-efficiency dialysers. This is the first report describing the effect of high-efficiency dialysers on lithium pharmacokinetic. Using this technique the elimination rate of lithium was found to be greater than previously reported with haemodialysis.

  14. Incommensurate Graphene Foam as a High Capacity Lithium Intercalation Anode

    Science.gov (United States)

    Paronyan, Tereza M.; Thapa, Arjun Kumar; Sherehiy, Andriy; Jasinski, Jacek B.; Jangam, John Samuel Dilip

    2017-01-01

    Graphite’s capacity of intercalating lithium in rechargeable batteries is limited (theoretically, 372 mAh g‑1) due to low diffusion within commensurately-stacked graphene layers. Graphene foam with highly enriched incommensurately-stacked layers was grown and applied as an active electrode in rechargeable batteries. A 93% incommensurate graphene foam demonstrated a reversible specific capacity of 1,540 mAh g‑1 with a 75% coulombic efficiency, and an 86% incommensurate sample achieves above 99% coulombic efficiency exhibiting 930 mAh g‑1 specific capacity. The structural and binding analysis of graphene show that lithium atoms highly intercalate within weakly interacting incommensurately-stacked graphene network, followed by a further flexible rearrangement of layers for a long-term stable cycling. We consider lithium intercalation model for multilayer graphene where capacity varies with N number of layers resulting LiN+1C2N stoichiometry. The effective capacity of commonly used carbon-based rechargeable batteries can be significantly improved using incommensurate graphene as an anode material.

  15. High Temperature Solid State Lithium Battery Project

    Data.gov (United States)

    National Aeronautics and Space Administration — Reliable energy systems with high energy density capable of operating at high temperatures, pressures and radiation levels are needed for certain NASA missions....

  16. Silver: high performance anode for thin film lithium ion batteries

    Science.gov (United States)

    Taillades, G.; Sarradin, J.

    Among metals and intermetallic compounds, silver exhibits a high specific capacity according to the formation of different Ag-Li alloys (up to AgLi 12) in a very low voltage range versus lithium (0.250-0 V). Electrochemical results including Galvanostatic Intermittent Titration Technique (GITT) as well as cycling behaviour experiments confirmed the interesting characteristics of silver thin film electrodes prepared by radio frequency (r.f.) sputtering. XRD patterns recorded at different electrochemical stages of the alloying/de-alloying processes showed the complexity of the silver-lithium system under dynamic conditions. Cycling life depends on several parameters and particularly of the careful choice of cut-off voltages. In very well monitored conditions, galvanostatic cycles exhibited flat reversible plateaus with a minimal voltage value (0.050 V) between charge and discharge, a feature of great interest in the use of an electrode. The first results of a lithium ion battery with both silver and LiMn 1.5Ni 0.5O 4 thin films are presented.

  17. PWR decontamination feasibility study

    Energy Technology Data Exchange (ETDEWEB)

    Silliman, P.L.

    1978-12-18

    The decontamination work which has been accomplished is reviewed and it is concluded that it is worthwhile to investigate further four methods for decontamination for future demonstration. These are: dilute chemical; single stage strong chemical; redox processes; and redox/chemical in combination. Laboratory work is recommended to define the agents and processes for demonstration and to determine the effect of the solvents on PWR materials. The feasibility of Indian Point 1 for decontamination demonstrations is discussed, and it is shown that the system components of Indian Point 1 are well suited for use in demonstrations.

  18. High temperature lithium cells with solid polymer electrolytes

    Energy Technology Data Exchange (ETDEWEB)

    Yang, Jin; Eitouni, Hany Basam; Singh, Mohit

    2017-03-07

    Electrochemical cells that use electrolytes made from new polymer compositions based on poly(2,6-dimethyl-1,4-phenylene oxide) and other high-softening-temperature polymers are disclosed. These materials have a microphase domain structure that has an ionically-conductive phase and a phase with good mechanical strength and a high softening temperature. In one arrangement, the structural block has a softening temperature of about 210.degree. C. These materials can be made with either homopolymers or with block copolymers. Such electrochemical cells can operate safely at higher temperatures than have been possible before, especially in lithium cells. The ionic conductivity of the electrolytes increases with increasing temperature.

  19. High throughput materials research and development for lithium ion batteries

    Directory of Open Access Journals (Sweden)

    Parker Liu

    2017-09-01

    Full Text Available Development of next generation batteries requires a breakthrough in materials. Traditional one-by-one method, which is suitable for synthesizing large number of sing-composition material, is time-consuming and costly. High throughput and combinatorial experimentation, is an effective method to synthesize and characterize huge amount of materials over a broader compositional region in a short time, which enables to greatly speed up the discovery and optimization of materials with lower cost. In this work, high throughput and combinatorial materials synthesis technologies for lithium ion battery research are discussed, and our efforts on developing such instrumentations are introduced.

  20. Studies Leading to the Development of High-Rate Lithium Sulfuryl Chloride Battery Technology.

    Science.gov (United States)

    1982-09-01

    greatest attention has been given to the lithium - thionyl chloride (Li/SOC12 ) system. Cells and batteries have been demonstrated with energy densities...Studies Leading to the Development of High-Rate Lithium Sulfuryl Chloride Battery Technology John C. Hall and Mark Koch Gould Research Center, Materials...High-Rate 11182to 33182 Lithium -Sulfuryl Chloride Battery Technology 1_1/82_to_3/31/82 S. PERFORMING ORO. REPORT NUMBER 2 7. AUTHOR(*) S. CONTRACT OR

  1. Evaluation of alternative descriptions of PWR cladding corrosion behavior

    Energy Technology Data Exchange (ETDEWEB)

    Quecedo, M.; Serna, J. J.; Weiner, R. A.; Kersting, P. J.

    1999-05-15

    A statistical procedure has been used to evaluate several alternative descriptions of pressurized water reactor (PWR) cladding corrosion behavior, using an extensive database of Improved (low tin) Zr-4 cladding corrosion measurements from fuel irradiated in commercial PWRs. The in-reactor corrosion enhancement factors considered in the model development are based on a comprehensive review of the current literature for PWR cladding corrosion phenomenology and models. In addition, because prediction of PWR cladding corrosion behavior is very sensitive to the values used for the oxide surface temperatures, several models for the forced convection and sub-cooled nucleate boiling (SNB) coolant heat transfer under PWR conditions have also been evaluated. This evaluation determined that the choice of the forced convection heat transfer has the greatest impact on the ability to fit the data. In addition, the SNB heat transfer model used must account for a continuous transition from forced convection conditions to fully developed SNB conditions. With these choices for the heat transfer models, the evaluation determined that the significant in-reactor corrosion enhancement factors are related to the formation of a hydride rim at the cladding outer diameter, the coolant lithium concentration, and the fast neutron fluence (author) (ml)

  2. Lithium rich cathode/graphite anode combination for lithium ion cells with high tolerance to near zero volt storage

    Science.gov (United States)

    Crompton, K. R.; Staub, J. W.; Hladky, M. P.; Landi, B. J.

    2017-03-01

    Management of reversible lithium is an advantageous approach to design lithium ion cells that are tolerant to near zero volt (NZV) storage under fixed resistive load towards highly controllable, enhanced user-inactive safety. Presently, the first cycle loss from a high energy density Li-rich HE5050 cathode is used to provide excess reversible lithium when paired with an appropriately capacity matched mesocarbon microbead (MCMB) anode. Cells utilizing 1.2 M LiPF6 3:7 v/v ethylene carbonate:ethyl methyl carbonate electrolyte and a lithium reference were used for 3-electrode testing. After conditioning, a fixed resistive load was applied to 3-electrode cells for 72 or 168-h during which the anode potential and electrode asymptotic potential (EAP) remained less than the copper dissolution potential. After multiple storage cycles (room temperature or 40 °C), the NZV coulombic efficiency (cell reversibility) exceeded 97% and the discharge capacity retention was >98%. Conventional 2-electrode HE5050/MCMB pouch cells stored at NZV or open circuit for 3 days had nearly identical rate capability (up to 5C) and discharge performance stability (for 500 cycles under a 30% depth of discharge low-earth-orbit regime). Thus, lithium ion cells with appropriately capacity matched HE5050/MCMB electrodes have excellent tolerance to prolonged NZV storage, which can lead to enhanced user-inactive safety.

  3. Compatibility of lithium plasma-facing surfaces with high edge temperatures in the Lithium Tokamak Experiment (LTX)

    Science.gov (United States)

    Majeski, Dick

    2016-10-01

    High edge electron temperatures (200 eV or greater) have been measured at the wall-limited plasma boundary in the Lithium Tokamak eXperiment (LTX). High edge temperatures, with flat electron temperature profiles, are a long-predicted consequence of low recycling boundary conditions. The temperature profile in LTX, measured by Thomson scattering, varies by as little as 10% from the plasma axis to the boundary, determined by the lithium-coated high field-side wall. The hydrogen plasma density in the outer scrape-off layer is very low, 2-3 x 1017 m-3 , consistent with a low recycling metallic lithium boundary. The plasma surface interaction in LTX is characterized by a low flux of high energy protons to the lithium PFC, with an estimated Debye sheath potential approaching 1 kV. Plasma-material interactions in LTX are consequently in a novel regime, where the impacting proton energy exceeds the peak in the sputtering yield for the lithium wall. In this regime, further increases in the edge temperature will decrease, rather than increase, the sputtering yield. Despite the high edge temperature, the core impurity content is low. Zeff is 1.2 - 1.5, with a very modest contribution (Gas puffing is used to increase the plasma density. After gas injection stops, the discharge density is allowed to drop, and the edge is pumped by the low recycling lithium wall. An upgrade to LTX which includes a 35A, 20 kV neutral beam injector to provide core fueling to maintain constant density, as well as auxiliary heating, is underway. Two beam systems have been loaned to LTX by Tri Alpha Energy. Additional results from LTX, as well as progress on the upgrade - LTX- β - will be discussed. Work supported by US DOE contracts DE-AC02-09CH11466 and DE-AC05-00OR22725.

  4. Development of Highly-Conductive Polyelectrolytes for Lithium Batteries

    Science.gov (United States)

    Shriver, D. F.; Ratner, M. A.; Vaynman, S.; Annan, K. O.; Snyder, J. F.

    2003-01-01

    Future NASA and Air Force missions require reliable and safe sources of energy with high specific energy and energy density that can provide thousands of charge-discharge cycles at more than 40% depth- of-discharge and that can operate at low temperatures. All solid-state batteries have substantial advantages with respect to stability, energy density, storage fife and cyclability. Among all solid-state batteries, those with flexible polymer electrolytes offer substantial advantages in cell dimensionality and commensurability, low temperature operation and thin film design. The above considerations suggest that lithium-polymer electrolyte systems are promising for high energy density batteries and should be the systems of choice for NASA and US Air Force applications. Polyelectrolytes (single ion conductors) are among most promising avenues for achieving a major breakthrough 'in the applicability of polymer- based electrolyte systems. Their major advantages include unit transference number for the cation, reduced cell polarization, minimal salt precipitation, and favorable electrolyte stability at interfaces. Our research is focused on synthesis, modeling and cell testing of single ion carriers, polyelectrolytes. During the first year of this project we attempted the synthesis of two polyelectrolytes. The synthesis of the first one, the poly(ethyleneoxide methoxy acrylateco-lithium 1,1,2-trifluorobutanesulfonate acrylate, was attempted few times and it was unsuccessful. We followed the synthetic route described by Cowie and Spence. The yield was extremely low and the final product could not be separated from the impurities. The synthesis of this polyelectrolyte is not described in this report. The second polyelectrolyte, comb polysiloxane polyelectrolyte containing oligoether and perfluoroether sidechains, was synthesized in sufficient quantity to study the range of properties such as thermal stability, Li- ion- conductivity and stability toward lithium metal. Also

  5. Electrochemical properties and lithium ion solvation behavior of sulfone-ester mixed electrolytes for high-voltage rechargeable lithium cells

    Science.gov (United States)

    Watanabe, Yuu; Kinoshita, Shin-ichi; Wada, Satoshi; Hoshino, Keiji; Morimoto, Hideyuki; Tobishima, Shin-ichi

    2008-05-01

    Sulfone-ester mixed solvent electrolytes were examined for 5 V-class high-voltage rechargeable lithium cells. As the base-electrolyte, sulfolane (SL)-ethyl acetate (EA) (1:1 mixing volume ratio) containing 1 M LiBF4 solute was investigated. Electrolyte conductivity, electrochemical stability, Li+ ion solvation behavior and cycleability of lithium electrode were evaluated. 13C NMR measurement results suggest that Li+ ions are solvated with both SL and EA. Charge-discharge cycling efficiency of lithium anode in SL-EA electrolytes was poor, being due to its poor tolerance for reduction. To improve lithium charge-discharge cycling efficiency in SL-EA electrolytes, following three trials were carried out: (i) improvement of the cathodic stability of electrolyte solutions by change in polarization through modification of solvent structure; isopropyl methyl sulfone and methyl isobutyrate were investigated as alternative SL and EA, respectively, (ii) suppression of the reaction between lithium and electrolyte solutions by addition of low reactivity surfactants of cycloalkanes (decalin and adamantane) or triethylene glycol derivatives (triglyme, 1,8-bis(tert-butyldimethylsilyloxy)-3,6-dioxaoctane and triethylene glycol di(methanesulfonate)) into SL-EA electrolytes, and (iii) change in surface film by addition of surface film formation agent of vinylene carbonate (VC) into SL-EA electrolytes. These trials made lithium cycling behavior better. Lithium cycling efficiency tended to increase with a decrease in overpotential. VC addition was most effective for improvement of lithium cycling efficiency among these additives. Stable surface film is formed on lithium anode by adding VC and the resistance between anode/electrolyte interfaces showed a constant value with an increase in cycle number. When the electrolyte solutions without VC, the interfacial resistance increased with an increase in cycle number. VC addition to SL-EA was effective not only for Li/LiCoO2 cell with charge

  6. Metallurgical and mechanical behaviours of PWR fuel cladding tube oxidised at high temperature; Comportements metallurqigue et mecanique des materiaux de gainage du combustible REP oxydes a haute temperature

    Energy Technology Data Exchange (ETDEWEB)

    Stern, A

    2007-12-15

    Zirconium alloys are used as cladding materials in Pressurized Water Reactors (PWR). As they are submitted to very extreme conditions, it is necessary to check their behaviour and especially to make sure they meet the safety criteria. They are therefore studied under typical in service-loadings but also under accidental loadings. In one of these accidental scenarios, called Loss of Coolant Accident (LOCA) the cladding temperature may increase above 800 C, in a steam environment, and decrease before a final quench of the cladding. During this temperature transient, the cladding is heavily oxidised, and the metallurgical changes lead to a decrease of the post quench mechanical properties. It is then necessary to correlate this drop in residual ductility to the metallurgical evolutions. This is the problem we want to address in this study: the oxidation of PWR cladding materials at high temperature in a steam environment and its consequences on post quench mechanical properties. As oxygen goes massively into the metallic part - a zirconia layer grows at the same time - during the high temperature oxidation, the claddings tubes microstructure shows three different phases that are the outer oxide layer (zirconia) and the inner metallic phases ({alpha}(O) and 'ex {beta}') - with various mechanical properties. In order to reproduce the behaviour of this multilayered material, the first part of this study consisted in creating samples with different - but homogeneous in thickness - oxygen contents, similar to those observed in the different phases of the real cladding. The study was especially focused on the {beta}-->{alpha} phase transformation upon cooling and on the resulting microstructures. A mechanism was proposed to describe this phase transformation. For instance, we conclude that for our oxygen enriched samples, the phase transformation kinetics upon cooling are ruled by the oxygen partitioning between the two allotropic phases. Then, these materials

  7. Nanoengineering Titania for High Rate Lithium Storage: A Review

    Institute of Scientific and Technical Information of China (English)

    Chunhai Jiang; Jinsong Zhang

    2013-01-01

    Nanostructured titania have been intensively investigated as anode materials of Li-ion batteries for their excellent high rate performance.The size effects of TiO2 polymorphs (mainly rutile,anatase and TiO2-B) on their electrochemical performance and the latest efforts in nanoengineering titania anodes through enhancing their ionic or electronic transportation or both are reviewed in this work.We suppose that micron-or submicronsized porous structures assembled by TiO2 nanoparticles,nanowires/nanotubes or nanosheets with a high percentage of exposing high reactive facets together with a conductive percolating network are ideal anodes not only for high rate lithium storage but also for high packing densities of the active materials.

  8. Nickel-rich layered lithium transition-metal oxide for high-energy lithium-ion batteries.

    Science.gov (United States)

    Liu, Wen; Oh, Pilgun; Liu, Xien; Lee, Min-Joon; Cho, Woongrae; Chae, Sujong; Kim, Youngsik; Cho, Jaephil

    2015-04-07

    High energy-density lithium-ion batteries are in demand for portable electronic devices and electrical vehicles. Since the energy density of the batteries relies heavily on the cathode material used, major research efforts have been made to develop alternative cathode materials with a higher degree of lithium utilization and specific energy density. In particular, layered, Ni-rich, lithium transition-metal oxides can deliver higher capacity at lower cost than the conventional LiCoO2 . However, for these Ni-rich compounds there are still several problems associated with their cycle life, thermal stability, and safety. Herein the performance enhancement of Ni-rich cathode materials through structure tuning or interface engineering is summarized. The underlying mechanisms and remaining challenges will also be discussed.

  9. Lithium-Ion Electrolytes with Improved Safety Tolerance to High Voltage Systems

    Science.gov (United States)

    Smart, Marshall C. (Inventor); Bugga, Ratnakumar V. (Inventor); Prakash, Surya G. (Inventor); Krause, Frederick C. (Inventor)

    2015-01-01

    The invention discloses various embodiments of electrolytes for use in lithium-ion batteries, the electrolytes having improved safety and the ability to operate with high capacity anodes and high voltage cathodes. In one embodiment there is provided an electrolyte for use in a lithium-ion battery comprising an anode and a high voltage cathode. The electrolyte has a mixture of a cyclic carbonate of ethylene carbonate (EC) or mono-fluoroethylene carbonate (FEC) co-solvent, ethyl methyl carbonate (EMC), a flame retardant additive, a lithium salt, and an electrolyte additive that improves compatibility and performance of the lithium-ion battery with a high voltage cathode. The lithium-ion battery is charged to a voltage in a range of from about 2.0 V (Volts) to about 5.0 V (Volts).

  10. High-rate lithium thionyl-chloride battery development

    Energy Technology Data Exchange (ETDEWEB)

    Cieslak, W.R.; Weigand, D.E.

    1993-12-31

    We have developed a lithium thionyl-chloride cell for use in a high rate battery application to provide power for a missile computer and stage separation detonators. The battery pack contains 20 high surface area ``DD`` cells wired in a series-parallel configuration to supply a nominal 28 volts with a continuous draw of 20 amperes. The load profile also requires six squib firing pulses of one second duration at a 20 ampere peak. Performance and safety of the cells were optimized in a ``D`` cell configuration before progressing to the longer ``DD` cell. Active surface area in the ``D`` cell is 735 cm{sup 2}, and 1650 cm{sup 2} in the ``DD`` cell. The design includes 1.5M LiAlCl{sub 4}/SOCl{sub 2} electrolyte, a cathode blend of Shawinigan Acetylene Black and Cabot Black Pearls 2000 carbons, Scimat ETFE separator, and photoetched current collectors.

  11. Advanced Cathode Material For High Energy Density Lithium-Batteries Project

    Data.gov (United States)

    National Aeronautics and Space Administration — Advanced cathode materials having high red-ox potential and high specific capacity offer great promise to the development of high energy density lithium-based...

  12. Performance Characterization of High Energy Commercial Lithium-ion Cells

    Science.gov (United States)

    Schneidegger, Brianne T.

    2010-01-01

    The NASA Glenn Research Center Electrochemistry Branch performed characterization of commercial lithium-ion cells to determine the cells' performance against Exploration Technology Development Program (ETDP) Key Performance Parameters (KPP). The goals of the ETDP Energy Storage Project require significant improvements in the specific energy of lithium-ion technology over the state-of-the-art. This work supports the high energy cell development for the Constellation customer Lunar Surface Systems (LSS). In support of these goals, testing was initiated in September 2009 with high energy cylindrical cells obtained from Panasonic and E-One Moli. Both manufacturers indicated the capability of their cells to deliver specific energy of at least 180 Wh/kg or higher. Testing is being performed at the NASA Glenn Research Center to evaluate the performance of these cells under temperature, rate, and cycling conditions relevant to the ETDP goals for high energy cells. The cell-level specific energy goal for high energy technology is 180 Wh/kg at a C/10 rate and 0 C. The threshold value is 165 Wh/kg. The goal is to operate for at least 2000 cycles at 100 percent DOD with greater than 80 percent capacity retention. The Panasonic NCR18650 cells were able to deliver nearly 200 Wh/kg at the aforementioned conditions. The E-One Moli ICR18650J cells also met the specific energy goal by delivering 183 Wh/kg. Though both cells met the goal for specific energy, this testing was only one portion of the testing required to determine the suitability of commercial cells for the ETDP. The cells must also meet goals for cycle life and safety. The results of this characterization are summarized in this report.

  13. A long-life lithium ion sulfur battery exploiting high performance electrodes.

    Science.gov (United States)

    Moreno, Noelia; Agostini, Marco; Caballero, Alvaro; Morales, Julián; Hassoun, Jusef

    2015-10-04

    A novel lithium ion sulfur battery is formed by coupling an activated ordered mesoporous carbon-sulfur (AOMC-S) cathode and a nanostructured tin-carbon anode. The lithium ion cell has improved reversibility, high energy content and excellent cycle life.

  14. High Energy Lithium-Ion VES Cells And Batteries Performances

    Science.gov (United States)

    Castric, A.-F.; Lawson, S.; Borthomieu, Y.

    2011-10-01

    b Saft's Space VES range of lithium-ion cells have been designed specifically to meet the satellites on-board power need, while meeting the legitimate high levels of requirements for space products. The purpose of the paper is to develop how the VES batteries designs have progressively evolved in order to accommodate the needs, requirements and constraints evolutions. The following topics will be presented: - Description of the main design features of the VES Li- ion batteries. - How the optimised battery configuration is selected against the required EOL power need or other constraints. - Presentation of the batteries performances (electrical, mechanical, thermal, interface, weight, ...). - Measures implemented in order to maintain these performances, and to guarantee the best product quality as per space standards.

  15. High flux lithium antineutrino source with variable hard spectrum

    CERN Document Server

    Lyashuk, V I

    2016-01-01

    The high flux antineutrino source with hard antineutrino spectrum based on neutron activation of 7Li and subsequent fast beta-decay (T 1/2 = 0.84 s) of the 8Li isotope with emission of antineutrino with energy up to 13 MeV - is discussed. Creation of the intensive isotope neutrino source of hard spectrum will allow to increase the detection statistics of neutrino interaction and it is especially urgent for oscillation experiments. The scheme of the proposed neutrino source is based on the continuous transport of the created 8Li to the neutrino detector, which moved away from the place of neutron activation. Analytical expressions for lithium antineutrino flux is obtained. The discussed source will ensure to increase the cross section for reactions with deuteron from several times to tens compare to the reactor antineutrino spectrum. An another unique feature of the installation is the possibility to vary smoothly the hardness of the antineutrino spectrum.

  16. Evolutionary developments of advanced PWR nuclear fuels and cladding materials

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Kyu-Tae, E-mail: ktkim@dongguk.ac.kr

    2013-10-15

    Highlights: • PWR fuel and cladding materials development processes are provided. • Evolution of PWR advanced fuel in U.S.A. and in Korea is described. • Cutting-edge design features against grid-to-rod fretting and debris are explained. • High performance data of advanced grids, debris filters and claddings are given. -- Abstract: The evolutionary developments of advanced PWR fuels and cladding materials are explained with outstanding design features of nuclear fuel assembly components and zirconium-base cladding materials. The advanced PWR fuel and cladding materials development processes are also provided along with verification tests, which can be used as guidelines for newcomers planning to develop an advanced fuel for the first time. The up-to-date advanced fuels with the advanced cladding materials may provide a high level of economic utilization and reliable performance even under current and upcoming aggressive operating conditions. To be specific, nuclear fuel vendors may achieve high fuel burnup capability of between 45,000 and 65,000 MWD/MTU batch average, overpower thermal margin of as much as 15% and longer cycle length up to 24 months on the one hand and fuel failure rates of around 10{sup −6} on the other hand. However, there is still a need for better understanding of grid-to-rod fretting wear mechanisms leading to major PWR fuel defects in the world and subsequently a driving force for developing innovative spacer grid designs with zero fretting wear-induced fuel failure.

  17. EPRI PWR Safety and Relief Valve Test Program: test condition justification report

    Energy Technology Data Exchange (ETDEWEB)

    Hosler, J.

    1982-12-01

    In response to NUREG 0737, Item II.D.1.A requirements, several safety and relief valve designs were tested by EPRI under PWR utility sponsorship. Justification that the inlet fluid conditions under which these valve designs were tested are representative of those expected in participating domestic PWR units during FSAR, Extended High Pressure Injection, and Cold Overpressurization events is presented.

  18. Positron-Lithium Atom and Electron-Lithium Atom Scattering Systems at Intermediate and High Energies

    Institute of Scientific and Technical Information of China (English)

    K. Ratnavelu; S. Y. Ng

    2006-01-01

    @@ The coupled-channel optical method is used to study positron scattering by atomic lithium at energies ranging from the ionization threshold to 60 eV. The present method simultaneously treats the target channels and the positronium (Ps) channels in the coupled-channel method together with the continuum effects via an ab-initio optical potential. Ionization, elastic and inelastic cross sections in target channels, and the total cross section are also reported and compared with other theoretical and experimental data. A comparative study with the corresponding electron-lithium data is also reported.

  19. Advances in lithium and calcium high-rate oxyhalide batteries

    Science.gov (United States)

    Hagan, W. P.; Green, S.; Sargeant, D. G.; Packer, R. K.

    The characteristics of lithium and calcium oxyhalide battery systems are considered, with special attention given to those of lithium-thionyl chloride and lithium-sulfuryl chloride cells. It is shown that, for a capability of above 50 mA/sq cm, lithium-sulfuryl chloride is the preferred cell chemistry, although calcium-thionyl chloride (which is acceptable up to 50 mA/sq cm) may be preferrable if thermal management is a problem. Lithium-sulfuryl chloride cells were found to exhibit a form of concentration polarization which is strongly dependent on interelectrode separation. In such cells, interelectrode separations have to be minimized if premature failure is to be avoided.

  20. Structurally tailored graphene nanosheets as lithium ion battery anodes: an insight to yield exceptionally high lithium storage performance.

    Science.gov (United States)

    Li, Xifei; Hu, Yuhai; Liu, Jian; Lushington, Andrew; Li, Ruying; Sun, Xueliang

    2013-12-21

    How to tune graphene nanosheets (GNSs) with various morphologies has been a significant challenge for lithium ion batteries (LIBs). In this study, three types of GNSs with varying size, edge sites, defects and layer numbers have been successfully achieved. It was demonstrated that controlling GNS morphology and microstructure has important effects on its cyclic performance and rate capability in LIBs. Diminished GNS layer number, decreased size, increased edge sites and increased defects in the GNS anode can be highly beneficial to lithium storage and result in increased electrochemical performance. Interestingly, GNSs treated with a hydrothermal approach delivered a high reversible discharge capacity of 1348 mA h g(-1). This study demonstrates that the controlled design of high performance GNS anodes is an important concept in LIB applications.

  1. Charge Localization in the Lithium Iron Phosphate Li3Fe2(PO4)3at High Voltages in Lithium-Ion Batteries

    DEFF Research Database (Denmark)

    Younesi, Reza; Christiansen, Ane Sælland; Loftager, Simon;

    2015-01-01

    Possible changes in the oxidation state of the oxygen ion in the lithium iron phosphate Li3Fe2(PO4)3 at high voltages in lithium-ion (Li-ion) batteries are studied using experimental and computational analysis. Results obtained from synchrotron-based hard X-ray photoelectron spectroscopy...

  2. Charge Localization in the Lithium Iron Phosphate Li3Fe2(PO4)3at High Voltages in Lithium-Ion Batteries

    DEFF Research Database (Denmark)

    Younesi, Reza; Christiansen, Ane Sælland; Loftager, Simon

    2015-01-01

    Possible changes in the oxidation state of the oxygen ion in the lithium iron phosphate Li3Fe2(PO4)3 at high voltages in lithium-ion (Li-ion) batteries are studied using experimental and computational analysis. Results obtained from synchrotron-based hard X-ray photoelectron spectroscopy...

  3. Fabricating high performance lithium-ion batteries using bionanotechnology

    Science.gov (United States)

    Zhang, Xudong; Hou, Yukun; He, Wen; Yang, Guihua; Cui, Jingjie; Liu, Shikun; Song, Xin; Huang, Zhen

    2015-02-01

    Designing, fabricating, and integrating nanomaterials are key to transferring nanoscale science into applicable nanotechnology. Many nanomaterials including amorphous and crystal structures are synthesized via biomineralization in biological systems. Amongst various techniques, bionanotechnology is an effective strategy to manufacture a variety of sophisticated inorganic nanomaterials with precise control over their chemical composition, crystal structure, and shape by means of genetic engineering and natural bioassemblies. This provides opportunities to use renewable natural resources to develop high performance lithium-ion batteries (LIBs). For LIBs, reducing the sizes and dimensions of electrode materials can boost Li+ ion and electron transfer in nanostructured electrodes. Recently, bionanotechnology has attracted great interest as a novel tool and approach, and a number of renewable biotemplate-based nanomaterials have been fabricated and used in LIBs. In this article, recent advances and mechanism studies in using bionanotechnology for high performance LIBs studies are thoroughly reviewed, covering two technical routes: (1) Designing and synthesizing composite cathodes, e.g. LiFePO4/C, Li3V2(PO4)3/C and LiMn2O4/C; and (2) designing and synthesizing composite anodes, e.g. NiO/C, Co3O4/C, MnO/C, α-Fe2O3 and nano-Si. This review will hopefully stimulate more extensive and insightful studies on using bionanotechnology for developing high-performance LIBs.

  4. Advancing High Energy Lithium-Sulfur Batteries Project

    Data.gov (United States)

    National Aeronautics and Space Administration — Lithium-Ion batteries have been a main source of energy for many aerospace applications over the past decade. Future space missions are facing a number of...

  5. High Capacity Anodes for Advanced Lithium Ion Batteries Project

    Data.gov (United States)

    National Aeronautics and Space Administration — Lithium-ion batteries are slowly being introduced into satellite power systems, but their life still presents concerns for longer duration missions. Future NASA...

  6. High energy lithium-oxygen batteries - Transport barriers and thermodynamics

    KAUST Repository

    Das, Shyamal K.

    2012-01-01

    We show that it is possible to achieve higher energy density lithium-oxygen batteries by simultaneously lowering the discharge overpotential and increasing the discharge capacity via thermodynamic variables alone. By assessing the relative effects of temperature and pressure on the cell discharge profiles, we characterize and diagnose the critical roles played by multiple dynamic processes that have hindered implementation of the lithium-oxygen battery. © 2012 The Royal Society of Chemistry.

  7. A Lithium-Air Battery with a High Energy Air Cathode Project

    Data.gov (United States)

    National Aeronautics and Space Administration — This project will advance an efficient and lightweight energy storage device for Oxygen Concentrators by developing a high specific energy lithium-air cell....

  8. Double carbon decorated lithium titanate as anode material with high rate performance for lithium-ion batteries

    Directory of Open Access Journals (Sweden)

    Haifang Ni

    2016-06-01

    Full Text Available Spinel lithium titanate (Li4Ti5O12 has the advantages of structural stability, however it suffers the disadvantages of low lithium-ion diffusion coefficient as well as low conductivity. In order to solve issues, we reported a simple method to prepare carbon-coated Li4Ti5O12/CNTs (C@Li4Ti5O12/CNTs using stearic acid as surfactant and carbon source to prepare carbon coated nanosized particles. The obtained Li4Ti5O12 particles of 100 nm in size are coated with the carbon layers pyrolyzed from stearic acid and dispersed in CNTs matrix homogeneously. These results show that the synthesized C@Li4Ti5O12/CNTs material used as anode materials for lithium ion batteries, presenting a better high-rate performance (147 mA h g−1 at 20 C. The key factors affecting the high-rate properties of the C@Li4Ti5O12/CNTs composite may be related to the synergistic effects of the CNTs matrix and the carbon- coating layers with conductivity enhancement. Additionally, the amorphous carbon coating is an effective route to ameliorate the rate capability of Li4Ti5O12/CNTs.

  9. Highly crystalline lithium titanium oxide sheets coated with nitrogen-doped carbon enable high-rate lithium-ion batteries.

    Science.gov (United States)

    Han, Cuiping; He, Yan-Bing; Li, Baohua; Li, Hongfei; Ma, Jun; Du, Hongda; Qin, Xianying; Yang, Quan-Hong; Kang, Feiyu

    2014-09-01

    Sheets of Li4Ti5O12 with high crystallinity are coated with nitrogen-doped carbon (NC-LTO) using a controlled process, comprising hydrothermal reaction followed by chemical vapor deposition (CVD). Acetonitrile (CH3 CN) vapor is used as carbon and nitrogen source to obtain a thin coating layer of nitrogen-doped carbon. The layer enables the NC-LTO material to maintain its sheet structure during the high-temperature CVD process and to achieve high crystallinity. Doping with nitrogen introduces defects into the carbon coating layer, and this increased degree of disorder allows fast transportation of lithium ions in the layer. An electrode of NC-LTO synthesized at 700 °C exhibits greatly improved rate and cycling performance due to a markedly decreased total cell resistance and enhanced Li-ion diffusion coefficient (D(Li)). Specific capacities of 159.2 and 145.8 mA h g(-1) are obtained using the NC-LTO sheets, at charge/discharge rates of 1 and 10 C, respectively. These values are much higher than values for LTO particles did not undergo the acetonitrile CVD treatment. A capacity retention value as high as 94.7% is achieved for the NC-LTO sheets after 400 cycles in a half-cell at 5 C discharge rate.

  10. Investigation of high-rate lithium-thionyl chloride cells

    Science.gov (United States)

    Hayes, Catherine A.; Gust, Steven; Farrington, Michael D.; Lockwood, Judith A.; Donaldson, George J.

    Chemical analysis of a commercially produced high-rate D-size lithium-thionyl cell was carried out, as a function of rate of discharge (1 ohm and 5 ohms), depth of discharge, and temperature (25 C and -40 C), using specially developed methods for identifying suspected minor cell products or impurities which may effect cell performance. These methods include a product-retrieval system which involves solvent extraction to enhance the recovery of suspected semivolatile minor chemicals, and methods of quantitative GC analysis of volatile and semivolatile products. The nonvolatile products were analyzed by wet chemical methods. The results of the analyses indicate that the predominant discharge reaction in this cell is 4Li + 2SOCl2 going to 4LiCl + S + SO2, with SO2 formation decreasing towards the end of cell life (7 to 12 Ah). The rate of discharge had no effect on the product distribution. Upon discharge of the high-rate cell at -40 C, one cell exploded, and all others exhibited overheating and rapid internal pressure rise when allowed to warm up to room temperature.

  11. A high power lithium thionyl chloride battery for space applications

    Science.gov (United States)

    Shah, Pinakin M.

    1993-03-01

    A high power, 28 V, 330 A h, active lithium thionyl chloride battery has been developed for use as main and payload power sources on an expendable launch vehicle. Nine prismatic cells, along with the required electrical components and a built-in heater system, are efficiently packaged resulting in significant weight savings over presently used silver-zinc batteries. The high rate capability is achieved by designing the cells with a large electrochemical surface area and impregnating an electrocatalyst, polymeric phthalocyanine, into the carbon cathodes. Passivation effects are reduced with the addition of sulfur dioxide into the thionyl chloride electrolyte solution. The results of conducting a detailed thermal analysis are utilized to establish the heater design parameters and the thermal insulation requirements of the battery. An analysis of cell internal pressure and vent characteristics clearly illustrates the margins of safety under different operating conditions. Performance of fresh cells is discussed using polarization scan and discharge data at different rates and temperatures. Self-discharge rate is estimated based upon test results on cells after storage. Results of testing a complete prototype battery are described.

  12. Mesoporous Nitrogen Doped Carbon-Glass Ceramic Cathode for High Performance Lithium-Oxygen Battery

    Science.gov (United States)

    2012-06-01

    Hardwick, and J.- M. Tarascon, Nature Materials, vol. 11, pp 19-29, 2012. 2. Linden , D. (Ed), Handbook of Batteries , 2nd Edition, Mc-Graw-Hill, New...AFRL-RQ-WP-TP-2015-0053 MESOPOROUS NITROGEN DOPED CARBON-GLASS CERAMIC CATHODE FOR HIGH PERFORMANCE LITHIUM-OXYGEN BATTERY (POSTPRINT...DOPED CARBON-GLASS CERAMIC CATHODE FOR HIGH PERFORMANCE LITHIUM-OXYGEN BATTERY (POSTPRINT) 5a. CONTRACT NUMBER In-house 5b. GRANT NUMBER 5c

  13. Electrochemical Performance of Highly Mesoporous Nitrogen Doped Carbon Cathode in Lithium-Oxygen Batteries (Postprint)

    Science.gov (United States)

    2011-03-01

    Chem. Lett. 1 (2010) 2193–2203. [3] F.T. Wagner, B. Lakshmanan, M.F. Mathias, J. Phys. Chem. Lett. 1 (2010) 2204–2219. [4] D. Linden (Ed.), Handbook ...AFRL-RQ-WP-TP-2015-0052 ELECTROCHEMICAL PERFORMANCE OF HIGHLY MESOPOROUS NITROGEN DOPED CARBON CATHODE IN LITHIUM-OXYGEN BATTERIES ...01 March 2011 4. TITLE AND SUBTITLE ELECTROCHEMICAL PERFORMANCE OF HIGHLY MESOPOROUS NITROGEN DOPED CARBON CATHODE IN LITHIUM-OXYGEN BATTERIES

  14. High rate lithium-sulfur battery enabled by sandwiched single ion conducting polymer electrolyte

    OpenAIRE

    Yubao Sun; Gai Li; Yuanchu Lai; Danli Zeng; Hansong Cheng

    2016-01-01

    Lithium-sulfur batteries are highly promising for electric energy storage with high energy density, abundant resources and low cost. However, the battery technologies have often suffered from a short cycle life and poor rate stability arising from the well-known “polysulfide shuttle” effect. Here, we report a novel cell design by sandwiching a sp 3 boron based single ion conducting polymer electrolyte film between two carbon films to fabricate a composite separator for lithium-sulfur batterie...

  15. Optical Properties of Lithium Terbium Fluoride and Implications for Performance in High Power Lasers (Postprint)

    Science.gov (United States)

    2016-02-01

    AFRL-RX-WP-JA-2016-0323 OPTICAL PROPERTIES OF LITHIUM TERBIUM FLUORIDE AND IMPLICATIONS FOR PERFORMANCE IN HIGH POWER LASERS...DATE (DD-MM-YY) 2. REPORT TYPE 3. DATES COVERED (From - To) 16 October 2015 Interim 6 May 2010 – 16 September 2015 4. TITLE AND SUBTITLE...OPTICAL PROPERTIES OF LITHIUM TERBIUM FLUORIDE AND IMPLICATIONS FOR PERFORMANCE IN HIGH POWER LASERS (POSTPRINT) 5a. CONTRACT NUMBER IN-HOUSE 5b

  16. Li-rich Li-Si alloy as a lithium-containing negative electrode material towards high energy lithium-ion batteries.

    Science.gov (United States)

    Iwamura, Shinichiroh; Nishihara, Hirotomo; Ono, Yoshitaka; Morito, Haruhiko; Yamane, Hisanori; Nara, Hiroki; Osaka, Tetsuya; Kyotani, Takashi

    2015-01-28

    Lithium-ion batteries (LIBs) are generally constructed by lithium-including positive electrode materials, such as LiCoO2, and lithium-free negative electrode materials, such as graphite. Recently, lithium-free positive electrode materials, such as sulfur, are gathering great attention from their very high capacities, thereby significantly increasing the energy density of LIBs. Though the lithium-free materials need to be combined with lithium-containing negative electrode materials, the latter has not been well developed yet. In this work, the feasibility of Li-rich Li-Si alloy is examined as a lithium-containing negative electrode material. Li-rich Li-Si alloy is prepared by the melt-solidification of Li and Si metals with the composition of Li21Si5. By repeating delithiation/lithiation cycles, Li-Si particles turn into porous structure, whereas the original particle size remains unchanged. Since Li-Si is free from severe constriction/expansion upon delithiation/lithiation, it shows much better cyclability than Si. The feasibility of the Li-Si alloy is further examined by constructing a full-cell together with a lithium-free positive electrode. Though Li-Si alloy is too active to be mixed with binder polymers, the coating with carbon-black powder by physical mixing is found to prevent the undesirable reactions of Li-Si alloy with binder polymers, and thus enables the construction of a more practical electrochemical cell.

  17. Preparation and characterization of high salts polymer electrolyte based on poly(lithium acrylate)

    Institute of Scientific and Technical Information of China (English)

    TANG Ai-dong; HUANG Ke-long; PAN Chun-yue; LU Cui-hong

    2005-01-01

    Novel polymer electrolytes were prepared by highly mixing poly(lithium acrylate)(PPALi) with eutectic lithium salts of lithium acetate and lithium nitrate.Poly(lithium acrylate) was preparaed by inverse emulsion polymerization from crylic acid and LiOH.Phase transition temperatures were measured for all the eutectic lithium of binary system samples as a function of the concentration of Li(CH3 COO),and the mixtures exhibit the lowest phase transition temperatures of (448±2) K at about 50% (mass fraction) Li(CH3 COO).Thermogravimetry(TG)and X-ray diffraction(XRD) analysis indicate the formation of a novel polymer-salt complex.The highest conductivity(approximately 4.97 ×10-5S·cm-1) is found at room temperature with the electrolyte composition of eutectic mixture of about 80% (mass fraction),poly(lithium acrylate) 20% under quickly cooling condition,which is 150%higher than that under natural cooling condition.

  18. Tracking inhomogeneity in high-capacity lithium iron phosphate batteries

    Science.gov (United States)

    Paxton, William A.; Zhong, Zhong; Tsakalakos, Thomas

    2015-02-01

    Energy-dispersive x-ray diffraction (EDXRD) is one of the few techniques that can internally probe a sealed battery under operating conditions. In this paper, we use EDXRD with ultrahigh energy synchrotron radiation to track inhomogeneity in a cycled high-capacity lithium iron phosphate cell under in-situ and operando conditions. A sequence of depth-profile x-ray diffraction spectra are collected with 40 μm resolution as the cell is discharged. Additionally, nine different locations of the cell are tracked independently throughout a second discharge process. In each case, a two-peak reference intensity ratio analysis (RIR) was used on the LiFePO4 311 and the FePO4 020 reflections to estimate the relative phase abundance of the lithiated and non-lithiated phases. The data provide a first-time look at the dynamics of electrochemical inhomogeneity in a real-world battery. We observe a strong correlation between inhomogeneity and overpotential in the galvanic response of the cell. Additionally, the data closely follow the behavior that is predicted by the resistive-reactant model originally proposed by Thomas-Alyea. Despite a non-linear response in the independently measured locations, the behavior of the ensemble is strikingly linear. This suggests that effects of inhomogeneity can be elusive and highlights the power of the EDXRD technique.

  19. Superconductivity of lithium-doped hydrogen under high pressure.

    Science.gov (United States)

    Xie, Yu; Li, Quan; Oganov, Artem R; Wang, Hui

    2014-02-01

    The high-pressure lattice dynamics and superconductivity of newly proposed lithium hydrides (LiH2, LiH6 and LiH8) have been extensively studied using density functional theory. The application of the Allen-Dynes modified McMillan equation and electron-phonon coupling calculations show that LiH6 and LiH8 are superconductors with critical temperatures (T(c)) of 38 K at 150 GPa for LiH6 and 31 K at 100 GPa for LiH8, while LiH2 is not a superconductor. The T(c) of LiH6 increases rapidly with pressure and reaches 82 K at 300 GPa due to enhancement of the electron-phonon coupling and the increased density of states at the Fermi level, while the T(c) of LiH8 remains almost constant.

  20. A highly reversible room-temperature lithium metal battery based on crosslinked hairy nanoparticles.

    KAUST Repository

    Choudhury, Snehashis

    2015-12-04

    Rough electrodeposition, uncontrolled parasitic side-reactions with electrolytes and dendrite-induced short-circuits have hindered development of advanced energy storage technologies based on metallic lithium, sodium and aluminium electrodes. Solid polymer electrolytes and nanoparticle-polymer composites have shown promise as candidates to suppress lithium dendrite growth, but the challenge of simultaneously maintaining high mechanical strength and high ionic conductivity at room temperature has so far been unmet in these materials. Here we report a facile and scalable method of fabricating tough, freestanding membranes that combine the best attributes of solid polymers, nanocomposites and gel-polymer electrolytes. Hairy nanoparticles are employed as multifunctional nodes for polymer crosslinking, which produces mechanically robust membranes that are exceptionally effective in inhibiting dendrite growth in a lithium metal battery. The membranes are also reported to enable stable cycling of lithium batteries paired with conventional intercalating cathodes. Our findings appear to provide an important step towards room-temperature dendrite-free batteries.

  1. High-flux neutron source based on a liquid-lithium target

    Science.gov (United States)

    Halfon, S.; Feinberg, G.; Paul, M.; Arenshtam, A.; Berkovits, D.; Kijel, D.; Nagler, A.; Eliyahu, I.; Silverman, I.

    2013-04-01

    A prototype compact Liquid Lithium Target (LiLiT), able to constitute an accelerator-based intense neutron source, was built. The neutron source is intended for nuclear astrophysical research, boron neutron capture therapy (BNCT) in hospitals and material studies for fusion reactors. The LiLiT setup is presently being commissioned at Soreq Nuclear research Center (SNRC). The lithium target will produce neutrons through the 7Li(p,n)7Be reaction and it will overcome the major problem of removing the thermal power generated by a high-intensity proton beam, necessary for intense neutron flux for the above applications. The liquid-lithium loop of LiLiT is designed to generate a stable lithium jet at high velocity on a concave supporting wall with free surface toward the incident proton beam (up to 10 kW). During off-line tests, liquid lithium was flown through the loop and generated a stable jet at velocity higher than 5 m/s on the concave supporting wall. The target is now under extensive test program using a high-power electron-gun. Up to 2 kW electron beam was applied on the lithium flow at velocity of 4 m/s without any flow instabilities or excessive evaporation. High-intensity proton beam irradiation will take place at SARAF (Soreq Applied Research Accelerator Facility) superconducting linear accelerator currently in commissioning at SNRC.

  2. Acute high dose lithium-induced exacerbation of obsessive compulsive symptoms.

    Science.gov (United States)

    Umesh, Shreekantiah; Sinha, Vinod Kumar

    2014-05-01

    Obsessive compulsive disorder (OCD) is a chronic neuropsychiatric disorder whose pathophysiology is linked to serotonergic dysfunction. More recently, the role of glutamate has also been posited. Lithium is used as an adjunctive for the treatment of OCD which is found to enhance serotonergic transmission. We present a case of OCD who was on stable dose of sertraline developed exacerbation of obsessive compulsive symptoms with acute high dose of lithium but improved after dose reduction.

  3. Silicon oxide based high capacity anode materials for lithium ion batteries

    Energy Technology Data Exchange (ETDEWEB)

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

    2017-03-21

    Silicon oxide based materials, including composites with various electrical conductive compositions, are formulated into desirable anodes. The anodes can be effectively combined into lithium ion batteries with high capacity cathode materials. In some formulations, supplemental lithium can be used to stabilize cycling as well as to reduce effects of first cycle irreversible capacity loss. Batteries are described with surprisingly good cycling properties with good specific capacities with respect to both cathode active weights and anode active weights.

  4. High-rate, long-life Ni-Sn nanostructured electrodes for lithium-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Hassoun, J.; Panero, S.; Scrosati, B. [Department of Chemistry, University of Rome ' ' La Sapienza' ' , P.le Aldo Moro 5, 00185 Rome (Italy); Simon, P.; Taberna, P.L. [CIRIMAT-UMR 5085 - Universite Paul Sabatier, route de Narbonne, 31062 Toulouse, Cedex 4 (France)

    2007-06-18

    Ni{sub 3}Sn{sub 4} intermetallic electrodes prepared into a revolutionary nanostructure, obtained by electrodeposition on a nanoarchitectured Cu substrate, are described. This structure controls the volume stress that accompanies the electrochemical process yielding a performance rarely observed with lithium metal storage electrodes. The new electrode shows impressive electrochemical behavior and cycles in lithium cells for more than 200 cycles with a stable high capacity. (Abstract Copyright [2007], Wiley Periodicals, Inc.)

  5. High-Performance Lithium-Air Battery with a Coaxial-Fiber Architecture.

    Science.gov (United States)

    Zhang, Ye; Wang, Lie; Guo, Ziyang; Xu, Yifan; Wang, Yonggang; Peng, Huisheng

    2016-03-24

    The lithium-air battery has been proposed as the next-generation energy-storage device with a much higher energy density compared with the conventional lithium-ion battery. However, lithium-air batteries currently suffer enormous problems including parasitic reactions, low recyclability in air, degradation, and leakage of liquid electrolyte. Besides, they are designed into a rigid bulk structure that cannot meet the flexible requirement in the modern electronics. Herein, for the first time, a new family of fiber-shaped lithium-air batteries with high electrochemical performances and flexibility has been developed. The battery exhibited a discharge capacity of 12,470 mAh g(-1) and could stably work for 100 cycles in air; its electrochemical performances were well maintained under bending and after bending. It was also wearable and formed flexible power textiles for various electronic devices.

  6. Dependence of recycling and edge profiles on lithium evaporation in high triangularity, high performance NSTX H-mode discharges

    Energy Technology Data Exchange (ETDEWEB)

    Maingi, R., E-mail: rmaingi@pppl.gov [Princeton Plasma Physics Laboratory, Receiving 3, Route 1 North, Princeton, NJ 08543 (United States); Osborne, T.H. [General Atomics, 3550 General Atomics Ct., San Diego, CA 92121 (United States); Bell, M.G.; Bell, R.E.; Boyle, D.P. [Princeton Plasma Physics Laboratory, Receiving 3, Route 1 North, Princeton, NJ 08543 (United States); Canik, J.M. [Oak Ridge National Laboratory, PO Box 2008, Oak Ridge, TN 37831 (United States); Diallo, A.; Kaita, R.; Kaye, S.M.; Kugel, H.W.; LeBlanc, B.P. [Princeton Plasma Physics Laboratory, Receiving 3, Route 1 North, Princeton, NJ 08543 (United States); Sabbagh, S.A. [Applied Physics and Applied Math Dept., Columbia University, New York, NY 10027 (United States); Skinner, C.H. [Princeton Plasma Physics Laboratory, Receiving 3, Route 1 North, Princeton, NJ 08543 (United States); Soukhanovskii, V.A. [Lawrence Livermore National Laboratory, 7000 East Ave, PO Box 808, Livermore, CA 94551 (United States)

    2015-08-15

    In this paper, the effects of a pre-discharge lithium evaporation variation on highly shaped discharges in the National Spherical Torus Experiment (NSTX) are documented. Lithium wall conditioning (‘dose’) was routinely applied onto graphite plasma facing components between discharges in NSTX, partly to reduce recycling. Reduced D{sub α} emission from the lower and upper divertor and center stack was observed, as well as reduced midplane neutral pressure; the magnitude of reduction increased with the pre-discharge lithium dose. Improved energy confinement, both raw τ{sub E} and H-factor normalized to scalings, with increasing lithium dose was also observed. At the highest doses, we also observed elimination of edge-localized modes. The midplane edge plasma profiles were dramatically altered, comparable to lithium dose scans at lower shaping, where the strike point was farther from the lithium deposition centroid. This indicates that the benefits of lithium conditioning should apply to the highly shaped plasmas planned in NSTX-U.

  7. Feasibility of Cathode Surface Coating Technology for High-Energy Lithium-ion and Beyond-Lithium-ion Batteries.

    Science.gov (United States)

    Kalluri, Sujith; Yoon, Moonsu; Jo, Minki; Liu, Hua Kun; Dou, Shi Xue; Cho, Jaephil; Guo, Zaiping

    2017-03-02

    Cathode material degradation during cycling is one of the key obstacles to upgrading lithium-ion and beyond-lithium-ion batteries for high-energy and varied-temperature applications. Herein, we highlight recent progress in material surface-coating as the foremost solution to resist the surface phase-transitions and cracking in cathode particles in mono-valent (Li, Na, K) and multi-valent (Mg, Ca, Al) ion batteries under high-voltage and varied-temperature conditions. Importantly, we shed light on the future of materials surface-coating technology with possible research directions. In this regard, we provide our viewpoint on a novel hybrid surface-coating strategy, which has been successfully evaluated in LiCoO2 -based-Li-ion cells under adverse conditions with industrial specifications for customer-demanding applications. The proposed coating strategy includes a first surface-coating of the as-prepared cathode powders (by sol-gel) and then an ultra-thin ceramic-oxide coating on their electrodes (by atomic-layer deposition). What makes it appealing for industry applications is that such a coating strategy can effectively maintain the integrity of materials under electro-mechanical stress, at the cathode particle and electrode- levels. Furthermore, it leads to improved energy-density and voltage retention at 4.55 V and 45 °C with highly loaded electrodes (≈24 mg.cm(-2) ). Finally, the development of this coating technology for beyond-lithium-ion batteries could be a major research challenge, but one that is viable. © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  8. A highly efficient polysulfide mediator for lithium-sulfur batteries

    Science.gov (United States)

    Liang, Xiao; Hart, Connor; Pang, Quan; Garsuch, Arnd; Weiss, Thomas; Nazar, Linda F.

    2015-01-01

    The lithium-sulfur battery is receiving intense interest because its theoretical energy density exceeds that of lithium-ion batteries at much lower cost, but practical applications are still hindered by capacity decay caused by the polysulfide shuttle. Here we report a strategy to entrap polysulfides in the cathode that relies on a chemical process, whereby a host—manganese dioxide nanosheets serve as the prototype—reacts with initially formed lithium polysulfides to form surface-bound intermediates. These function as a redox shuttle to catenate and bind ‘higher’ polysulfides, and convert them on reduction to insoluble lithium sulfide via disproportionation. The sulfur/manganese dioxide nanosheet composite with 75 wt% sulfur exhibits a reversible capacity of 1,300 mA h g-1 at moderate rates and a fade rate over 2,000 cycles of 0.036%/cycle, among the best reported to date. We furthermore show that this mechanism extends to graphene oxide and suggest it can be employed more widely.

  9. Methods of synthesis and performance improvement of lithium iron phosphate for high rate Li-ion batteries: A review

    Directory of Open Access Journals (Sweden)

    T.V.S.L. Satyavani

    2016-03-01

    Full Text Available Lithium ion battery technology has the potential to meet the requirements of high energy density and high power density applications. A continuous search for novel materials is pursued continually to exploit the latent potential of this technology. In this review paper, methods for preparation of Lithium Iron Phosphate are discussed which include solid state and solution based synthesis routes. The methods to improve the electrochemical performance of lithium iron phosphate are presented in detail.

  10. Methods of synthesis and performance improvement of lithium iron phosphate for high rate Li-ion batteries: A review

    OpenAIRE

    T.V.S.L. Satyavani; Srinivas Kumar, A.; P.S.V. Subba Rao

    2016-01-01

    Lithium ion battery technology has the potential to meet the requirements of high energy density and high power density applications. A continuous search for novel materials is pursued continually to exploit the latent potential of this technology. In this review paper, methods for preparation of Lithium Iron Phosphate are discussed which include solid state and solution based synthesis routes. The methods to improve the electrochemical performance of lithium iron phosphate are presented in d...

  11. Electrochemically fabricated polypyrrole-cobalt-oxygen coordination complex as high-performance lithium-storage materials.

    Science.gov (United States)

    Guo, Bingkun; Kong, Qingyu; Zhu, Ying; Mao, Ya; Wang, Zhaoxiang; Wan, Meixiang; Chen, Liquan

    2011-12-23

    Current lithium-ion battery (LIB) technologies are all based on inorganic electrode materials, though organic materials have been used as electrodes for years. Disadvantages such as limited thermal stability and low specific capacity hinder their applications. On the other hand, the transition metal oxides that provide high lithium-storage capacity by way of electrochemical conversion reaction suffer from poor cycling stability. Here we report a novel high-performance, organic, lithium-storage material, a polypyrrole-cobalt-oxygen (PPy-Co-O) coordination complex, with high lithium-storage capacity and excellent cycling stability. Extended X-ray absorption fine structure and Raman spectroscopy and other physical and electrochemical characterizations demonstrate that this coordination complex can be electrochemically fabricated by cycling PPy-coated Co(3)O(4) between 0.0 V and 3.0 V versus Li(+)/Li. Density functional theory (DFT) calculations indicate that each cobalt atom coordinates with two nitrogen atoms within the PPy-Co coordination layer and the layers are connected with oxygen atoms between them. Coordination weakens the C-H bonds on PPy and makes the complex a novel lithium-storage material with high capacity and high cycling stability.

  12. The prospects of phosphorene as an anode material for high-performance lithium-ion batteries: a fundamental study

    Science.gov (United States)

    Zhang, Congyan; Yu, Ming; Anderson, George; Ravinath Dharmasena, Ruchira; Sumanasekera, Gamini

    2017-02-01

    To completely understand lithium adsorption, diffusion, and capacity on the surface of phosphorene and, therefore, the prospects of phosphorene as an anode material for high-performance lithium-ion batteries (LIBs), we carried out density-functional-theory calculations and studied the lithium adsorption energy landscape, the lithium diffusion mobility, the lithium intercalation, and the lithium capacity of phosphorene. We also carried out, for the very first time, experimental measurement of the lithium capacity of phosphorene. Our calculations show that the lithium diffusion mobility along the zigzag direction in the valley of phosphorene was about 7 to 11 orders of magnitude faster than that along the other directions, indicating its ultrafast and anisotropic diffusivity. The lithium intercalation in phosphorene was studied by considering various Li n P16 configurations (n = 1-16) including single-side and double-side adsorptions. We found that phosphorene could accommodate up to a ratio of one Li per P atom (i.e. Li16P16). In particular, we found that, even at a high Li concentration (e.g. x = 1 in Li x P), there was no lithium clustering, and the structure of phosphorene (when fractured) is reversible during lithium intercalation. The theoretical value of the lithium capacity for a monolayer phosphorene is predicted to be above 433 mAh g-1, depending on whether Li atoms are adsorbed on the single side or the double side of phosphorene. Our experimental measurement of the lithium capacity for few-layer phosphorene networks shows a reversible stable value of ˜453 mAh g-1 even after 50 cycles. Our results clearly show that phosphorene, compared to graphene and other two-dimensional materials, has great promise as a novel anode material for high-performance LIBs.

  13. Materials and mechanisms of high temperature lithium sulfide batteries

    Energy Technology Data Exchange (ETDEWEB)

    Kaun, T.D.; Hash, M.C.; Henriksen, G.L.; Jansen, A.N.; Vissers, D.R.

    1994-05-01

    New materials have encouraged development of bipolar Li-Al/FeS{sub 2} batteries for electric vehicle (EV) applications. Current technology employs a two-phase Li-alloy negative electrode low-melting, LiCl-rich LiCl-LiBr-KBr molten salt electrolyte, and either an FeS or an upper-plateau (UP) FeS{sub 2} positive electrode. These components are assembled in a sealed bipolar battery configuration. Use of the two-phase Li-alloy ({alpha} + {beta} Li-Al and Li{sub 5}Al{sub 5}Fe{sub 2}) negative electrode provides in situ overcharge tolerance that renders the bipolar design viable. Employing LiCl-rich LiCl-LiBr-KBr electrolyte in ``electrolyte-starved`` calls achieves low-burdened cells, that possess low area-specific impedance; comparable to that of flooded cells using LiCl-LiBr-KBr eutectic electrolyte. The combination of dense UP FeS{sub 2} electrodes and low-melting electrolyte produces a stable and reversible couple, achieving over 1000 cycle life in flooded cells, with high power capabilities. In addition, a family of stable sulfide ceramic/sealant materials was developed that produce high-strength bonds between a variety of metals and ceramics, which renders lithium/iron suffide bipolar stacks practical. Bipolar Li-Al/FeS{sub 2} cells and four-cell stacks using these seals are being built and tested in the 13 cm diameter size for EV applications. To date, Li-Al/FeS{sub 2} cells have attained 400 W/kg power at 80% DOD and 180 Wh/kg energy at the 30 W/kg rate. When cell performance characteristics are used to model full-scale EV and hybrid vehicle (HV) batteries, they are projected to meet or exceed the performance requirements for a large variety of EV and HV applications. Efficient production and application of Li-alloys and Li-salt electrolyte are critical to approaching battery cost objectives.

  14. Permselective graphene oxide membrane for highly stable and anti-self-discharge lithium-sulfur batteries.

    Science.gov (United States)

    Huang, Jia-Qi; Zhuang, Ting-Zhou; Zhang, Qiang; Peng, Hong-Jie; Chen, Cheng-Meng; Wei, Fei

    2015-03-24

    Lithium-sulfur batteries hold great promise for serving as next generation high energy density batteries. However, the shuttle of polysulfide induces rapid capacity degradation and poor cycling stability of lithium-sulfur cells. Herein, we proposed a unique lithium-sulfur battery configuration with an ultrathin graphene oxide (GO) membrane for high stability. The oxygen electronegative atoms modified GO into a polar plane, and the carboxyl groups acted as ion-hopping sites of positively charged species (Li(+)) and rejected the transportation of negatively charged species (Sn(2-)) due to the electrostatic interactions. Such electrostatic repulsion and physical inhibition largely decreased the transference of polysulfides across the GO membrane in the lithium-sulfur system. Consequently, the GO membrane with highly tunable functionalization properties, high mechanical strength, low electric conductivity, and facile fabrication procedure is an effective permselective separator system in lithium-sulfur batteries. By the incorporation of a permselective GO membrane, the cyclic capacity decay rate is also reduced from 0.49 to 0.23%/cycle. As the GO membrane blocks the diffusion of polysulfides through the membrane, it is also with advantages of anti-self-discharge properties.

  15. High-power liquid-lithium target prototype for accelerator-based boron neutron capture therapy.

    Science.gov (United States)

    Halfon, S; Paul, M; Arenshtam, A; Berkovits, D; Bisyakoev, M; Eliyahu, I; Feinberg, G; Hazenshprung, N; Kijel, D; Nagler, A; Silverman, I

    2011-12-01

    A prototype of a compact Liquid-Lithium Target (LiLiT), which will possibly constitute an accelerator-based intense neutron source for Boron Neutron Capture Therapy (BNCT) in hospitals, was built. The LiLiT setup is presently being commissioned at Soreq Nuclear Research Center (SNRC). The liquid-lithium target will produce neutrons through the (7)Li(p,n)(7)Be reaction and it will overcome the major problem of removing the thermal power generated using a high-intensity proton beam (>10 kW), necessary for sufficient neutron flux. In off-line circulation tests, the liquid-lithium loop generated a stable lithium jet at high velocity, on a concave supporting wall; the concept will first be tested using a high-power electron beam impinging on the lithium jet. High intensity proton beam irradiation (1.91-2.5 MeV, 2-4 mA) will take place at Soreq Applied Research Accelerator Facility (SARAF) superconducting linear accelerator currently in construction at SNRC. Radiological risks due to the (7)Be produced in the reaction were studied and will be handled through a proper design, including a cold trap and appropriate shielding. A moderator/reflector assembly is planned according to a Monte Carlo simulation, to create a neutron spectrum and intensity maximally effective to the treatment and to reduce prompt gamma radiation dose risks.

  16. PWR fuel in Japan; The changes and trend for hereafter

    Energy Technology Data Exchange (ETDEWEB)

    Yokote, Mitsuhiro (Kansai Electric Power Co., Inc., Osaka (Japan)); Kondo, Yoshiaki; Abeta, Sadaaki

    1992-07-01

    As for the PWR fuel in Japan, much efforts have been exerted aiming at the high reliability since the start of operation of Mihama No. 1 plant of Kansai Electric Power Co., Inc. At the beginning of 1970s, the fuel made by Westinghouse in USA was imported, and since then, the pursuit of the causes of troubles and the countermeasures and the domestic production of fuel have been carried out, and the improvement of design and the strengthening of quality control have been advanced. As the results, the occurrence of troubles decreased rapidly. As the fuel improvement for hereafter, the economical improvement by higher burnup, the saving and effective use of uranium resources as well as the increase of reliability are emphasized. The changes in the PWR fuel by Westinghouse, the course of improvement in the PWR fuel in Japan, the improvement against the troubles of the fuel, the improved design, the verification of the performance of the PWR fuel, the trend of development of the fuel such as the heightening of burnup, the saving and effective use of uranium resources, and the improved type pressurized water reactors are reported. (K.I.).

  17. Physics of hydride fueled PWR

    Science.gov (United States)

    Ganda, Francesco

    The first part of the work presents the neutronic results of a detailed and comprehensive study of the feasibility of using hydride fuel in pressurized water reactors (PWR). The primary hydride fuel examined is U-ZrH1.6 having 45w/o uranium: two acceptable design approaches were identified: (1) use of erbium as a burnable poison; (2) replacement of a fraction of the ZrH1.6 by thorium hydride along with addition of some IFBA. The replacement of 25 v/o of ZrH 1.6 by ThH2 along with use of IFBA was identified as the preferred design approach as it gives a slight cycle length gain whereas use of erbium burnable poison results in a cycle length penalty. The feasibility of a single recycling plutonium in PWR in the form of U-PuH2-ZrH1.6 has also been assessed. This fuel was found superior to MOX in terms of the TRU fractional transmutation---53% for U-PuH2-ZrH1.6 versus 29% for MOX---and proliferation resistance. A thorough investigation of physics characteristics of hydride fuels has been performed to understand the reasons of the trends in the reactivity coefficients. The second part of this work assessed the feasibility of multi-recycling plutonium in PWR using hydride fuel. It was found that the fertile-free hydride fuel PuH2-ZrH1.6, enables multi-recycling of Pu in PWR an unlimited number of times. This unique feature of hydride fuels is due to the incorporation of a significant fraction of the hydrogen moderator in the fuel, thereby mitigating the effect of spectrum hardening due to coolant voiding accidents. An equivalent oxide fuel PuO2-ZrO2 was investigated as well and found to enable up to 10 recycles. The feasibility of recycling Pu and all the TRU using hydride fuels were investigated as well. It was found that hydride fuels allow recycling of Pu+Np at least 6 times. If it was desired to recycle all the TRU in PWR using hydrides, the number of possible recycles is limited to 3; the limit is imposed by positive large void reactivity feedback.

  18. Integrated high quality factor lithium niobate microdisk resonators

    CERN Document Server

    Wang, Cheng; Lin, Zin; Atikian, Haig A; Venkataraman, Vivek; Huang, I-Chun; Stark, Peter; Lončar, Marko

    2014-01-01

    Lithium Niobate (LN) is an important nonlinear optical material. Here we demonstrate LN microdisk resonators that feature optical quality factor ~ 100,000, realized using robust and scalable fabrication techniques, that operate over a wide wavelength range spanning visible and near infrared. Using our resonators, and leveraging LN's large second order optical nonlinearity, we demonstrate on-chip second harmonic generation with a conversion efficiency of 0.109 W-1.

  19. Nanocatalysis for Primary and Secondary High Energy Lithium Oxygen Cells

    Science.gov (United States)

    2011-04-01

    included emulsified Teflon (Fuel Cell Earth, 60 wt% in water), and mixtures of styrene butadiene latex ( SBR , Euclid Chemical Company) and sodium...They were, emulsified PTFE (60wt%), 2:1 (by weight) SBR /CMC blend, and lithium acrylate. Figure 43 Comarative perfomence of cahodes containing 6...the oxygen reduction reaction in fuel cell cathodes by nitrogen doped carbon (obtained via pyrolysis of N-containing polymers) has been well

  20. High Performance Pillared Vanadium Oxide Cathode for Lithium Ion Batteries

    Science.gov (United States)

    2015-04-24

    Automotive Research Development and Engineering Center, Warren, MI 48387, USA Keywords: nanostructured materials, lithium ion batteries, cathode... key consideration for batteries used in vehicle applications, the rate capability, cyclability, and safety of LIBs have been identified as critical...diffraction planes ( Figure 1). With the intercalation of the Al13 Keggin pillars, the position of the 001 plane shifts to 6.7 degrees two-theta, along with

  1. Three-dimensional tungsten nitride nanowires as high performance anode material for lithium ion batteries

    Science.gov (United States)

    Zhang, Min; Qiu, Yongfu; Han, Yi; Guo, Yan; Cheng, Faliang

    2016-08-01

    Nanostructure materials often achieve low capacity when the active material mass loading is high. In this communication, high mass-loading tungsten nitride nanowires (WNNWs) were fabricated on a flexible carbon cloth by hydrothermal method and post annealing. The prepared electrode exhibited remarkable cyclic stability and attractive rate capability for lithium storage. It delivers at a current density of 200 mA g-1, a high capacity of 418 mAh g-1, which is higher than that of conventional graphite. This research opens more opportunity for the fabrication of three-dimensional metal nitrides as negative electrode material for flexible lithium ion batteries.

  2. Nano-structured electrocatalysts for high performance lithium sulfur batteries

    Science.gov (United States)

    Mosavati, Negar

    Ni nanoparticles has been investigated as a carbon-free cathode material for dissolved polysulfide Li-S battery. A series of Ni nanoparticles with nominal particle size of 20, 40, and 100 nm have been used as electrocatalysts, and the effect of particle size on Li-S battery performance has been investigated. In addition, graphene has been chosen as a support to anchor the Ni nanoparticles, and the synergetic effect of carbon material and Ni nanoparticles on Li-S battery electrochemical performance has been studied. The results indicated there is a strong particle size effect. Ni/graphene electrode exhibits a capacity of 753 mAh g-1 sulfur after 40 cycles due to its high conductivity and electrocatalytic activity toward polysulfide reduction reaction. This capacity is significantly higher than similar studies. Based on the understanding of the electrocathalytic effect of Ni and capacity fading mechanism, transition metal nitrides has been investigated as a new class of cathode materials. Titanium nitride (TiN) nanoparticle was studied as a novel cathode material for Li/dissolved polysulfide batteries. In addition, X-ray photoelectron spectroscopy (XPS) analysis was used to obtain a deeper understanding of the mechanism underlying polysulfide conversion reactions with TiN cathode, and during charge and discharge processes. TiN exhibited a superior performance in a Li/dissolved polysulfide battery configuration. Knowing the superior performance of TiN, the study was expanded to different transition metal nitrides to investigate the role of surface composition and morphology in enhancing the electrochemical performance of Li-S batteries. WN, Mo2N, and VN were synthesized and the electrochemical performance, surface composition, and oxidation/reduction mechanism of these cathodes electrodes were studied for lithium sulfur batteries. Understanding the fading mechanisms of dissolved polysulfide system for metal nitride cathodes, It was tried to enhance Li-S battery

  3. Lithium iron phosphate/carbon nanocomposite film cathodes for high energy lithium ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Liu Yanyi; Liu Dawei; Zhang Qifeng [Department of Materials Science and Engineering, University of Washington, Seattle, WA 98195 (United States); Yu Danmei [Department of Materials Science and Engineering, University of Washington, Seattle, WA 98195 (United States); College of Chemistry and Chemical Engineering, Chongqing University, Chongqing 400044 (China); Liu Jun [Pacific Northwest National Laboratory, 902 Battelle Boulevard, P.O. Box 999, Richland, WA 99352 (United States); Cao Guozhong, E-mail: gzcao@u.washington.ed [Department of Materials Science and Engineering, University of Washington, Seattle, WA 98195 (United States)

    2011-02-01

    This paper reports sol-gel derived nanostructured LiFePO{sub 4}/carbon nanocomposite film cathodes exhibiting enhanced electrochemical properties and cyclic stabilities. LiFePO{sub 4}/carbon films were obtained by spreading sol on Pt coated Si wafer followed by ambient drying overnight and annealing/pyrolysis at elevated temperature in nitrogen. Uniform and crack-free LiFePO{sub 4}/carbon nanocomposite films were readily obtained and showed olivine phase as determined by means of X-Ray Diffractometry. The electrochemical characterization revealed that, at a current density of 200 mA/g (1.2 C), the nanocomposite film cathodes demonstrated an initial lithium-ion intercalation capacity of 312 mAh/g, and 218 mAh/g after 20 cycles, exceeding the theoretical storage capacity of conventional LiFePO{sub 4} electrode. Such enhanced Li-ion intercalation performance could be attributed to the nanocomposite structure with fine crystallite size below 20 nm as well as the poor crystallinity which provides a partially open structure allowing easy mass transport and volume change associated with Li-ion intercalation. Moreover the surface defect introduced by carbon nanocoating could also effectively facilitate the charge transfer and phase transitions.

  4. Lithium iron phosphate/carbon nanocomposite film cathodes for high energy lithium ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Yanyi; Liu, Dawei; Zhang, Qifeng; Yu, Danmei; Liu, Jun; Cao, Guozhong

    2011-02-01

    This paper reports sol-gel derived nanostructured LiFePO4/carbon nanocomposite film cathodes exhibiting enhanced electrochemical properties and cyclic stabilities. LiFePO4/carbon films were obtained by spreading sol on Pt coated Si wafer followed by ambient drying overnight and annealing/pyrolysis at elevated temperature in nitrogen. Uniform and crack-free LiFePO4/carbon nanocomposite films were readily obtained and showed olivine phase as determined by means of X-Ray Diffractometry. The electrochemical characterization revealed that, at a current density of 200 mA/g (1.2 C), the nanocomposite film cathodes demonstrated an initial lithium-ion intercalation capacity of 312 mAh/g, and 218 mAh/g after 20 cycles, exceeding the theoretical storage capacity of conventional LiFePO4 electrode. Such enhanced Li-ion intercalation performance could be attributed to the nanocomposite structure with fine crystallite size below 20 nm as well as the poor crystallinity which provides a partially open structure allowing easy mass transport and volume change associated with Li-ion intercalation. Moreover the surface defect introduced by carbon nanocoating could also effectively facilitate the charge transfer and phase transitions.

  5. High-Energy All-Solid-State Lithium Batteries with Ultralong Cycle Life.

    Science.gov (United States)

    Yao, Xiayin; Liu, Deng; Wang, Chunsheng; Long, Peng; Peng, Gang; Hu, Yong-Sheng; Li, Hong; Chen, Liquan; Xu, Xiaoxiong

    2016-11-09

    High energy and power densities are the greatest challenge for all-solid-state lithium batteries due to the poor interfacial compatibility between electrodes and electrolytes as well as low lithium ion transfer kinetics in solid materials. Intimate contact at the cathode-solid electrolyte interface and high ionic conductivity of solid electrolyte are crucial to realizing high-performance all-solid-state lithium batteries. Here, we report a general interfacial architecture, i.e., Li7P3S11 electrolyte particles anchored on cobalt sulfide nanosheets, by an in situ liquid-phase approach. The anchored Li7P3S11 electrolyte particle size is around 10 nm, which is the smallest sulfide electrolyte particles reported to date, leading to an increased contact area and intimate contact interface between electrolyte and active materials. The neat Li7P3S11 electrolyte synthesized by the same liquid-phase approach exhibits a very high ionic conductivity of 1.5 × 10(-3) S cm(-1) with a particle size of 0.4-1.0 μm. All-solid-state lithium batteries employing cobalt sulfide-Li7P3S11 nanocomposites in combination with the neat Li7P3S11 electrolyte and Super P as the cathode and lithium metal as the anode exhibit excellent rate capability and cycling stability, showing reversible discharge capacity of 421 mAh g(-1) at 1.27 mA cm(-2) after 1000 cycles. Moreover, the obtained all-solid-state lithium batteries possesses very high energy and power densities, exhibiting 360 Wh kg(-1) and 3823 W kg(-1) at current densities of 0.13 and 12.73 mA cm(-2), respectively. This contribution demonstrates a new interfacial design for all-solid-state battery with high performance.

  6. Sulfonic Groups Originated Dual-Functional Interlayer for High Performance Lithium-Sulfur Battery.

    Science.gov (United States)

    Lu, Yang; Gu, Sui; Guo, Jing; Rui, Kun; Chen, Chunhua; Zhang, Sanpei; Jin, Jun; Yang, Jianhua; Wen, Zhaoyin

    2017-05-03

    The lithium-sulfur battery is one of the most prospective chemistries in secondary energy storage field due to its high energy density and high theoretical capacity. However, the dissolution of polysulfides in liquid electrolytes causes the shuttle effect, and the rapid decay of lithium sulfur battery has greatly hindered its practical application. Herein, combination of sulfonated reduced graphene oxide (SRGO) interlayer on the separator is adopted to suppress the shuttle effect. We speculate that this SRGO layer plays two roles: physically blocking the migration of polysulfide as ion selective layer and anchoring lithium polysulfide by the electronegative sulfonic group. Lewis acid-base theory and density functional theory (DFT) calculations indicate that sulfonic groups have a strong tendency to interact with lithium ions in the lithium polysulfide. Hence, the synergic effect involved by the sulfonic group contributes to the enhancement of the battery performance. Furthermore, the uniformly distributed sulfonic groups working as active sites which could induce the uniform distribution of sulfur, alleviating the excessive growth of sulfur and enhancing the utilization of active sulfur. With this interlayer, the prototype battery exhibits a high reversible discharge capacity of more than 1300 mAh g(-1) and good capacity retention of 802 mAh g(-1) after 250 cycles at 0.5 C rate. After 60 cycles at different rates from 0.2 to 4 C, the cell with this functional separator still recovered a high specific capacity of 1100 mAh g(-1) at 0.2 C. The results demonstrate a promising interlayer design toward high performance lithium-sulfur battery with longer cycling life, high specific capacity, and rate capability.

  7. High-power liquid-lithium jet target for neutron production

    CERN Document Server

    Halfon, S; Kijel, D; Paul, M; Berkovits, D; Eliyahu, I; Feinberg, G; Friedman, M; Hazenshprung, N; Mardor, I; Nagler, A; Shimel, G; Tessler, M; Silverman, I

    2013-01-01

    A compact Liquid-Lithium Target (LiLiT) was built and tested with a high-power electron gun at Soreq Nuclear Research Center. The lithium target, to be bombarded by the high-intensity proton beam of the Soreq Applied Research Accelerator Facility (SARAF), will constitute an intense source of neutrons produced by the 7Li(p,n)7Be reaction for nuclear astrophysics research and as a pilot setup for accelerator-based Boron Neutron Capture Therapy (BNCT). The liquid-lithium jet target acts both as neutron-producing target and beam dump by removing the beam thermal power (>5 kW, >1 MW/cm3) with fast transport. The target was designed based on a thermal model, accompanied by a detailed calculation of the 7Li(p,n) neutron yield, energy distribution and angular distribution. Liquid lithium is circulated through the target loop at ~200oC and generates a stable 1.5 mm-thick film flowing at a velocity up to 7 m/s onto a concave supporting wall. Electron beam irradiation demonstrated that the liquid-lithium target can diss...

  8. Li2C2, a High-Capacity Cathode Material for Lithium Ion Batteries.

    Science.gov (United States)

    Tian, Na; Gao, Yurui; Li, Yurong; Wang, Zhaoxiang; Song, Xiaoyan; Chen, Liquan

    2016-01-11

    As a typical alkaline earth metal carbide, lithium carbide (Li2C2) has the highest theoretical specific capacity (1400 mA h g(-1)) among all the reported lithium-containing cathode materials for lithium ion batteries. Herein, the feasibility of using Li2C2 as a cathode material was studied. The results show that at least half of the lithium can be extracted from Li2C2 and the reversible specific capacity reaches 700 mA h g(-1). The C≡C bond tends to rotate to form C4 (C≡C⋅⋅⋅C≡C) chains during lithium extraction, as indicated with the first-principles molecular dynamics (FPMD) simulation. The low electronic and ionic conductivity are believed to be responsible for the potential gap between charge and discharge, as is supported with density functional theory (DFT) calculations and Arrhenius fitting results. These findings illustrate the feasibility to use the alkali and alkaline earth metal carbides as high-capacity electrode materials for secondary batteries.

  9. Performance and Degradation of A Lithium-Bromine Rechargeable Fuel Cell Using Highly Concentrated Catholytes

    CERN Document Server

    Bai, Peng

    2016-01-01

    Lithium-air batteries have been considered as ultimate solutions for the power source of long-range electrified transportation, but state-of-the-art prototypes still suffer from short cycle life, low efficiency and poor power output. Here, a lithium-bromine rechargeable fuel cell using highly concentrated bromine catholytes is demonstrated with comparable specific energy, improved power density, and higher efficiency. The cell is similar in structure to a hybrid-electrolyte Li-air battery, where a lithium metal anode in nonaqueous electrolyte is separated from aqueous bromine catholytes by a lithium-ion conducting ceramic plate. The cell with a flat graphite electrode can discharge at a peak power density around 9mW cm-2 and in principle could provide a specific energy of 791.8 Wh kg-1, superior to most existing cathode materials and catholytes. It can also run in regenerative mode to recover the lithium metal anode and free bromine with 80-90% voltage efficiency, without any catalysts. Degradation of the sol...

  10. New family of lithium salts for highly conductive nonaqueous electrolytes.

    Science.gov (United States)

    Barbarich, Thomas J; Driscoll, Peter F; Izquierdo, Suzette; Zakharov, Lev N; Incarvito, Christopher D; Rheingold, Arnold L

    2004-11-29

    New lithium salts of weakly coordinating anions were prepared by treating lithium imidazolates or LiN(CH3)2 with 2 equiv of BF(3). They are LiIm(BF3)2, Li 2-MeIm(BF3)2, Li 4-MeIm(BF3)2, LiBenzIm(BF3)2, Li 2-iPrIm(BF3)2, and LiN(CH3)2(BF3)2 (Im=imidazolate, Me=methyl, iPr=isopropyl, BenzIm=benzoimidazolate). The salts were characterized by NMR spectroscopy and mass spectrometry. The structure of LiBenzIm(BF3)2 consists of a dimeric centrosymmetric unit with each lithium atom forming a bridge between the two anions through one fluorine contact to each anion. The structure of a hydrate of LiN(CH3)2(BF3)2 consists of an infinite chain in which each anion chelates two different lithium atoms through Li-F bonds. The conductivities of electrolyte solutions of these salts were measured and are discussed in terms of different ion-pairing modes determined from the solid-state structures, the anion's ability to distribute charge, and solution viscosity. Organic carbonate solutions of LiIm(BF3)2 partially disproportionate at 85 degrees C forming LiBF4, LiBF2[Im(BF3)]2, and Li[(BF3)ImBF2ImBF2Im(BF3)], reaching equilibrium by 3 months at 85 degrees C but not disproportionating at room temperature after 9 months. A mechanism for the formation of these disproportionation products is proposed. The lower conductivity of the 1 M LiIm(BF3)2 solution that has undergone disproportionation is attributed to the formation LiBF4, which is less conductive, and LiBF2[Im(BF3)]2 and Li[(BF3)ImBF2ImBF2Im(BF3)], which increase solution viscosity.

  11. High voltage cathode compositions for lithium-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Lu, Zhonghua; Eberman, Kevin W

    2017-03-21

    A lithium transition metal oxide composition. The composition has the formula Li.sub.a[Li.sub.bNi.sub.cMn.sub.dCo.sub.e]O.sub.2, where a.gtoreq.0.9, b.gtoreq.0, c>0, d>0, e>0, b+c+d+e=1, 1.05.ltoreq.c/d.ltoreq.1.4, 0.05.ltoreq.e.ltoreq.0.30, 0.9.ltoreq.(a+b)/M.ltoreq.1.06, and M=c+d+e. The composition has an O3 type structure.

  12. In-operando high-speed tomography of lithium-ion batteries during thermal runaway

    Science.gov (United States)

    Finegan, Donal P.; Scheel, Mario; Robinson, James B.; Tjaden, Bernhard; Hunt, Ian; Mason, Thomas J.; Millichamp, Jason; di Michiel, Marco; Offer, Gregory J.; Hinds, Gareth; Brett, Dan J. L.; Shearing, Paul R.

    2015-04-01

    Prevention and mitigation of thermal runaway presents one of the greatest challenges for the safe operation of lithium-ion batteries. Here, we demonstrate for the first time the application of high-speed synchrotron X-ray computed tomography and radiography, in conjunction with thermal imaging, to track the evolution of internal structural damage and thermal behaviour during initiation and propagation of thermal runaway in lithium-ion batteries. This diagnostic approach is applied to commercial lithium-ion batteries (LG 18650 NMC cells), yielding insights into key degradation modes including gas-induced delamination, electrode layer collapse and propagation of structural degradation. It is envisaged that the use of these techniques will lead to major improvements in the design of Li-ion batteries and their safety features.

  13. High catalytic activity of anatase titanium dioxide for decomposition of electrolyte solution in lithium ion battery

    Science.gov (United States)

    Liu, Ming; He, Yan-Bing; Lv, Wei; Zhang, Chen; Du, Hongda; Li, Baohua; Yang, Quan-Hong; Kang, Feiyu

    2014-12-01

    It has been indicated that anatase TiO2 is a promising anode material for lithium ion power battery from many previous researches. Whereas, in this work, we find that the anatase TiO2, when used as an anode for lithium ion battery, has high catalytic activity to initiate the decarboxylation reaction of electrolyte solution, resulting in the large generation of sole gaseous component, CO2. The ROLi species and the new phase of flake-like Li2TiF6 material are the main reaction products between anatase TiO2 and LiPF6 based electrolyte solution. This work provides important and urgent information that the surface chemistry of anatase TiO2 used as the anode material of lithium ion battery must be modified to suppress its catalytic activity for the decomposition of solvents.

  14. In-operando high-speed tomography of lithium-ion batteries during thermal runaway.

    Science.gov (United States)

    Finegan, Donal P; Scheel, Mario; Robinson, James B; Tjaden, Bernhard; Hunt, Ian; Mason, Thomas J; Millichamp, Jason; Di Michiel, Marco; Offer, Gregory J; Hinds, Gareth; Brett, Dan J L; Shearing, Paul R

    2015-04-28

    Prevention and mitigation of thermal runaway presents one of the greatest challenges for the safe operation of lithium-ion batteries. Here, we demonstrate for the first time the application of high-speed synchrotron X-ray computed tomography and radiography, in conjunction with thermal imaging, to track the evolution of internal structural damage and thermal behaviour during initiation and propagation of thermal runaway in lithium-ion batteries. This diagnostic approach is applied to commercial lithium-ion batteries (LG 18650 NMC cells), yielding insights into key degradation modes including gas-induced delamination, electrode layer collapse and propagation of structural degradation. It is envisaged that the use of these techniques will lead to major improvements in the design of Li-ion batteries and their safety features.

  15. Graphene oxide as a sulfur immobilizer in high performance lithium/sulfur cells

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Yuegang; Cairns, Elton J.; Ji, Liwen; Rao, Mumin

    2017-06-06

    The loss of sulfur cathode material as a result of polysulfide dissolution causes significant capacity fading in rechargeable lithium/sulfur cells. Embodiments of the invention use a chemical approach to immobilize sulfur and lithium polysulfides via the reactive functional groups on graphene oxide. This approach obtains a uniform and thin (.about.tens of nanometers) sulfur coating on graphene oxide sheets by a chemical reaction-deposition strategy and a subsequent low temperature thermal treatment process. Strong interaction between graphene oxide and sulfur or polysulfides demonstrate lithium/sulfur cells with a high reversible capacity of 950-1400 mAh g.sup.-1, and stable cycling for more than 50 deep cycles at 0.1 C.

  16. In-operando high-speed tomography of lithium-ion batteries during thermal runaway

    Science.gov (United States)

    Finegan, Donal P.; Scheel, Mario; Robinson, James B.; Tjaden, Bernhard; Hunt, Ian; Mason, Thomas J.; Millichamp, Jason; Di Michiel, Marco; Offer, Gregory J.; Hinds, Gareth; Brett, Dan J.L.; Shearing, Paul R.

    2015-01-01

    Prevention and mitigation of thermal runaway presents one of the greatest challenges for the safe operation of lithium-ion batteries. Here, we demonstrate for the first time the application of high-speed synchrotron X-ray computed tomography and radiography, in conjunction with thermal imaging, to track the evolution of internal structural damage and thermal behaviour during initiation and propagation of thermal runaway in lithium-ion batteries. This diagnostic approach is applied to commercial lithium-ion batteries (LG 18650 NMC cells), yielding insights into key degradation modes including gas-induced delamination, electrode layer collapse and propagation of structural degradation. It is envisaged that the use of these techniques will lead to major improvements in the design of Li-ion batteries and their safety features. PMID:25919582

  17. A Highly Thermostable Ceramic-Grafted Microporous Polyethylene Separator for Safer Lithium-Ion Batteries.

    Science.gov (United States)

    Zhu, Xiaoming; Jiang, Xiaoyu; Ai, Xinping; Yang, Hanxi; Cao, Yuliang

    2015-11-04

    The safety concern is a critical obstacle to large-scale energy storage applications of lithium-ion batteries. A thermostable separator is one of the most effective means to construct the safe lithium-ion batteries. Herein, we demonstrate a novel ceramic (SiO2)-grafted PE separator prepared by electron beam irradiation. The separator shows similar thickness and pore structure to the bare separator, while displaying strong dimensional thermostability, as the shrinkage ratio is only 20% even at an elevated temperature of 180 °C. Besides, the separator is highly electrochemically inert, showing no adverse effect on the energy and power output of the batteries. Considering the excellent electrochemical and thermal stability, the SiO2-grafted PE separator developed in this work is greatly beneficial for constructing safer lithium-ion batteries.

  18. Nuclear quantum and electronic exchange-correlation effects on the high pressure phase diagram of lithium

    Science.gov (United States)

    Clay, Raymond; Morales, Miguel; Bonev, Stanimir

    Lithium at ambient conditions is the simplest alkali metal and exhibits textbook nearly-free electron character. However, increased core/valence electron overlap under compression leads to surprisingly complex behavior. Dense lithium is known to posses a maximum in the melting line, a metal to semiconductor phase transition around 80GPa, reemergent metallicity around 120GPa, and low coordination solid and liquid phases. In addition to its complex electronic structure at high pressure, the atomic mass of lithium is low enough that nuclear quantum effects could have a nontrivial impact on its phase diagram. Through a combination of density functional theory based path-integral and classical molecular dynamics simulations, we have investigated the impact of both nuclear quantum effects and anharmonicity on the melting line and solid phase boundaries. Additionally, we have determined the robustness of previously predicted tetrahedral clustering in the dense liquid to the inclusion of nuclear quantum effects and approximate treatment of electronic exchange-correlation effects.

  19. Response of NSTX liquid lithium divertor to high heat loads

    Energy Technology Data Exchange (ETDEWEB)

    Abrams, T., E-mail: tabrams@pppl.gov [Princeton Plasma Physics Laboratory, Princeton, NJ 08543 (United States); Jaworski, M.A. [Princeton Plasma Physics Laboratory, Princeton, NJ 08543 (United States); Kallman, J. [Lawrence Livermore National Laboratory, Livermore, CA 94550 (United States); Kaita, R. [Princeton Plasma Physics Laboratory, Princeton, NJ 08543 (United States); Foley, E.L. [Nova Photonics, Inc., Princeton, NJ 08543 (United States); Gray, T.K. [Oak Ridge National Laboratory, Oak Ridge, TN 37831 (United States); Kugel, H. [Princeton Plasma Physics Laboratory, Princeton, NJ 08543 (United States); Levinton, F. [Nova Photonics, Inc., Princeton, NJ 08543 (United States); McLean, A.G. [Lawrence Livermore National Laboratory, Livermore, CA 94550 (United States); Skinner, C.H. [Princeton Plasma Physics Laboratory, Princeton, NJ 08543 (United States)

    2013-07-15

    Samples of the NSTX Liquid Lithium Divertor (LLD) with and without an evaporative Li coating were directly exposed to a neutral beam ex-situ at a power of ∼1.5 MW/m{sup 2} for 1–3 s. Measurements of front face and bulk sample temperature were obtained. Predictions of temperature evolution were derived from a 1D heat flux model. No macroscopic damage occurred when the “bare” sample was exposed to the beam but microscopic changes to the surface were observed. The Li-coated sample developed a lithium hydroxide (LiOH) coating, which did not change even when the front face temperature exceeded the pure Li melting point. These results are consistent with the lack of damage to the LLD surface and imply that heating alone may not expose pure liquid Li if the melting point of surface impurities is not exceeded. This suggests that flow and heat are needed for future PFCs requiring a liquid Li surface.

  20. 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.

  1. High performance lithium insertion negative electrode materials for electrochemical devices

    Science.gov (United States)

    Channu, V. S. Reddy; Rambabu, B.; Kumari, Kusum; Kalluru, Rajmohan R.; Holze, Rudolf

    2016-11-01

    Spinel LiCrTiO4 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 LiCrTiO4 electrode were examined in a lithium ion battery. The electrode prepared with oxalic acid-assisted LiCrTiO4 shows higher specific capacity.This LiCrTiO4 is also used as anode material for an asymmetric hybrid supercapacitor. The cell exhibits a specific capacity of 65 mAh/g at 1 mA/cm2. The specific capacity decreases with increasing current densities.

  2. Zebra: An advanced PWR lattice code

    Energy Technology Data Exchange (ETDEWEB)

    Cao, L.; Wu, H.; Zheng, Y. [School of Nuclear Science and Technology, Xi' an Jiaotong Univ., No. 28, Xianning West Road, Xi' an, ShannXi, 710049 (China)

    2012-07-01

    This paper presents an overview of an advanced PWR lattice code ZEBRA developed at NECP laboratory in Xi'an Jiaotong Univ.. The multi-group cross-section library is generated from the ENDF/B-VII library by NJOY and the 361-group SHEM structure is employed. The resonance calculation module is developed based on sub-group method. The transport solver is Auto-MOC code, which is a self-developed code based on the Method of Characteristic and the customization of AutoCAD software. The whole code is well organized in a modular software structure. Some numerical results during the validation of the code demonstrate that this code has a good precision and a high efficiency. (authors)

  3. La2O3 hollow nanospheres for high performance lithium-ion rechargeable batteries.

    Science.gov (United States)

    Sasidharan, Manickam; Gunawardhana, Nanda; Inoue, Masamichi; Yusa, Shin-ichi; Yoshio, Masaki; Nakashima, Kenichi

    2012-03-28

    An efficient and simple protocol for synthesis of novel La(2)O(3) hollow nanospheres of size about 30 ± 2 nm using polymeric micelles is reported. The La(2)O(3) hollow nanospheres exhibit high charge capacity and cycling performance in lithium-ion rechargeable batteries (LIBs), which was scrutinized for the first time among the rare-earth oxides.

  4. In situ growth of MOFs on the surface of si nanoparticles for highly efficient lithium storage: Si@MOF nanocomposites as anode materials for lithium-ion batteries.

    Science.gov (United States)

    Han, Yuzhen; Qi, Pengfei; Feng, Xiao; Li, Siwu; Fu, Xiaotao; Li, Haiwei; Chen, Yifa; Zhou, Junwen; Li, Xingguo; Wang, Bo

    2015-02-04

    A simple yet powerful one-pot strategy is developed to prepare metal-organic framework-coated silicon nanoparticles via in situ mechanochemical synthesis. After simple pyrolysis, the thus-obtained composite shows exceptional electrochemical properties with a lithium storage capacity up to 1050 mA h g(-1), excellent cycle stability (>99% capacity retention after 500 cycles) and outstanding rate performance. These characteristics, combined with their high stability and ease of fabrication, make such Si@MOF nanocomposites ideal alternative candidates as high-energy anode materials in lithium-ion batteries.

  5. Reviving the lithium metal anode for high-energy batteries

    Science.gov (United States)

    Lin, Dingchang; Liu, Yayuan; Cui, Yi

    2017-03-01

    Lithium-ion batteries have had a profound impact on our daily life, but inherent limitations make it difficult for Li-ion chemistries to meet the growing demands for portable electronics, electric vehicles and grid-scale energy storage. Therefore, chemistries beyond Li-ion are currently being investigated and need to be made viable for commercial applications. The use of metallic Li is one of the most favoured choices for next-generation Li batteries, especially Li-S and Li-air systems. After falling into oblivion for several decades because of safety concerns, metallic Li is now ready for a revival, thanks to the development of investigative tools and nanotechnology-based solutions. In this Review, we first summarize the current understanding on Li anodes, then highlight the recent key progress in materials design and advanced characterization techniques, and finally discuss the opportunities and possible directions for future development of Li anodes in applications.

  6. Robust, High Capacity, High Power Lithium Ion Batteries for Space Systems Project

    Data.gov (United States)

    National Aeronautics and Space Administration — Lithium ion battery technology provides the highest energy density of all rechargeable battery technologies available today. However, the majority of the research...

  7. Microwave exfoliated graphene oxide/TiO2 nanowire hybrid for high performance lithium ion battery

    Science.gov (United States)

    Ishtiaque Shuvo, Mohammad Arif; Rodriguez, Gerardo; Islam, Md Tariqul; Karim, Hasanul; Ramabadran, Navaneet; Noveron, Juan C.; Lin, Yirong

    2015-09-01

    Lithium ion battery (LIB) is a key solution to the demand of ever-improving, high energy density, clean-alternative energy systems. In LIB, graphite is the most commonly used anode material; however, lithium-ion intercalation in graphite is limited, hindering the battery charge rate and capacity. To date, one of the approaches in LIB performance improvement is by using porous carbon (PC) to replace graphite as anode material. PC's pore structure facilitates ion transport and has been proven to be an excellent anode material candidate in high power density LIBs. In addition, to overcome the limited lithium-ion intercalation obstacle, nanostructured anode assembly has been extensively studied to increase the lithium-ion diffusion rate. Among these approaches, high specific surface area metal oxide nanowires connecting nanostructured carbon materials accumulation have shown promising results for enhanced lithium-ion intercalation. Herein, we demonstrate a hydrothermal approach of growing TiO2 nanowires (TON) on microwave exfoliated graphene oxide (MEGO) to further improve LIB performance over PC. This MEGO-TON hybrid not only uses the high surface area of MEGO but also increases the specific surface area for electrode-electrolyte interaction. Therefore, this new nanowire/MEGO hybrid anode material enhances both the specific capacity and charge-discharge rate. Scanning electron microscopy and X-ray diffraction were used for materials characterization. Battery analyzer was used for measuring the electrical performance of the battery. The testing results have shown that MEGO-TON hybrid provides up to 80% increment of specific capacity compared to PC anode.

  8. 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

  9. Superior Thermally Stable and Nonflammable Porous Polybenzimidazole Membrane with High Wettability for High-Power Lithium-Ion Batteries.

    Science.gov (United States)

    Li, Dan; Shi, Dingqin; Xia, Yonggao; Qiao, Lin; Li, Xianfeng; Zhang, Huamin

    2017-02-28

    Separators with high security, reliability, and rate capacity are in urgent need for the advancement of high power lithium ion batteries. The currently used porous polyolefin membranes are critically hindered by their low thermal stability and poor electrolyte wettability, which further lead to low rate capacity. Here we present a novel promising porous polybenzimidazole (PBI) membrane with super high thermal stability and electrolyte wettability. The rigid structure and functional groups in the PBI chain enable membranes to be stable at temperature as high as 400 °C, and the unique flame resistance of PBI could ensure the high security of a battery as well. In particular, the prepared membrane owns 328% electrolyte uptake, which is more than two times higher than commercial Celgard 2325 separator. The unique combination of high thermal stability, high flame resistance and super high electrolyte wettability enable the PBI porous membranes to be highly promising for high power lithium battery.

  10. Functional Organosulfide Electrolyte Promotes an Alternate Reaction Pathway to Achieve High Performance in Lithium-Sulfur Batteries.

    Science.gov (United States)

    Chen, Shuru; Dai, Fang; Gordin, Mikhail L; Yu, Zhaoxin; Gao, Yue; Song, Jiangxuan; Wang, Donghai

    2016-03-18

    Lithium-sulfur (Li-S) batteries have recently received great attention because they promise to provide energy density far beyond current lithium ion batteries. Typically, Li-S batteries operate by conversion of sulfur to reversibly form different soluble lithium polysulfide intermediates and insoluble lithium sulfides through multistep redox reactions. Herein, we report a functional electrolyte system incorporating dimethyl disulfide as a co-solvent that enables a new electrochemical reduction pathway for sulfur cathodes. This pathway uses soluble dimethyl polysulfides and lithium organosulfides as intermediates and products, which can boost cell capacity and lead to improved discharge-charge reversibility and cycling performance of sulfur cathodes. This electrolyte system can potentially enable Li-S batteries to achieve high energy density.

  11. Control of corrosion product transport in PWR secondary cycles

    Energy Technology Data Exchange (ETDEWEB)

    Sawochka, S.G.; Pearl, W.L. [NWT Corp., San Josa, CA (United States); Passell, T.O.; Welty, C.S. [Electric Power Research Institute, Palo Alto, CA (United States)

    1992-12-31

    Transport of corrosion products to PWR steam generators by the feedwater leads to sludge buildup on the tubesheets and fouling of tube-to-tube support crevices. In these regions, chemical impurities concentrate and accelerate tubing corrosion. Deposit buildup on the tubes also can lead to power generation limitations and necessitate chemical cleaning. Extensive corrosion product transport data for PWR secondary cycles has been developed employing integrating sampling techniques which facilitate identification of major corrosion product sources and assessments of the effectiveness of various control options. Plant data currently are available for assessing the impact of factors such as pH, pH control additive, materials of construction, blowdown, condensate treatment, and high temperature drains and feedwater filtration.

  12. The responses of rainbow trout gills to high lithium and potassium concentrations in water.

    Science.gov (United States)

    Tkatcheva, Victoria; Holopainen, Ismo J; Hyvärinen, Heikki; Kukkonen, Jussi V K

    2007-11-01

    The objective of this study is to discern the effects of increased waterborne lithium and potassium on rainbow trout gill histology, lipid composition, and enzyme activity. The study aims to elucidate the effects of these ions in the laboratory in concentrations similar to those prevailing in a forest lake Poppalijärvi in a contaminated mining area in NW Russia. Under the lithium and potassium exposure, the fish were further stressed by high pH (8.2 as in Lake Poppalijärvi) and lack of food. These multiple stress conditions altered the gill membrane fluidity by increasing sphingomyelin (5.5+/-0.6 compared to 2.9+/-0.3% in the control) and reducing cholesterol (4+/-1 compared to 17+/-3 mg g(-1) in the control). The total ATPase activity tended to be higher in the lithium-potassium-exposed group (46+/-6 compared to 34+/-2 micromol Pi h(-1) mg(-1)protein in the control). Lithium toxicity was lowered here by the protective role of higher potassium contents.

  13. Fabrication of highly ordered porous nickel oxide anode materials and their electrochemical characteristics in lithium storage

    Energy Technology Data Exchange (ETDEWEB)

    Miao, Fengjuan [College of Communications and Electronics Engineering, Qiqihar University, 42 Wenhua Street, Qiqihar, Heilongjiang 161006 (China); National Laboratory for Infrared Physics, Shanghai Institute of Technical Physics, Chinese Academy of Sciences, Shanghai 200083 (China); Li, Qianqian [College of Communications and Electronics Engineering, Qiqihar University, 42 Wenhua Street, Qiqihar, Heilongjiang 161006 (China); Tao, Bairui, E-mail: tbr_sir@163.com [Computer Center, Qiqihar University, 42 Wenhua Street, Qiqihar, Heilongjiang 161006 (China); National Laboratory for Infrared Physics, Shanghai Institute of Technical Physics, Chinese Academy of Sciences, Shanghai 200083 (China); Chu, Paul K. [Department of Physics and Material Sciences, City University of Hong Kong, Tat Chee Avenue, Kowloon, Hong Kong (China)

    2014-05-01

    Highlights: • NiO/Si-MCP nanocomposites electrocatalysts as anodes in lithium ion batteries. • Si MCP itself is an excellent support for electrocatalyst. • The structure with high surface to volume ratio endows higher mass NiO nanopatricles. • The ordered channel and mesoporous structure permits liquid electrolyte flow easily. • This research may provide a meaning way in integratable lithium-ion batteries. - Abstract: The structure and electrochemical properties of silicon microchannel plates (MCP)-supported NiO nanocomposites (NiO/Si-MCP) synthesized by silicon micromachining, electroless plating, and thermal annealing are investigated as anodes in lithium ion batteries. Galvanostatic charge and discharge results indicate that the NiO/Si-MCP is capable of delivering a higher capacity than the bare nickel-oxide film. At a 1 C current, the NiO/Si-MCP nanocomposite film shows an enormous first discharge capacity of about 3190 mA g{sup −1} and charge capacity of 1977 mA g{sup −1}. After 15 cycles, the NiO/Si-MCP nanocomposite retains a reversible capacity of 1531 mA g{sup −1} with 63.7% of the capacity maintained in the 2nd cycle. The lithium storage capacity is maintained at ∼880 mA h g{sup −1} after 50 discharge/charge cycles and it is much larger than that of NiO and its composites. The enhanced electrochemical performance of the highly ordered three-dimensional materials is attributed to the synergistic effects offered by the silicon microchannel plates in the nickel oxide film subsequently facilitating electrolyte penetration, diffusion, and migration. The structure is promising anode materials in lithium-ion batteries.

  14. Lithium Germanate (Li2 GeO3 ): A High-Performance Anode Material for Lithium-Ion Batteries.

    Science.gov (United States)

    Rahman, Md Mokhlesur; Sultana, Irin; Yang, Tianyu; Chen, Zhiqiang; Sharma, Neeraj; Glushenkov, Alexey M; Chen, Ying

    2016-12-23

    A simple, cost-effective, and easily scalable molten salt method for the preparation of Li2 GeO3 as a new type of high-performance anode for lithium-ion batteries is reported. The Li2 GeO3 exhibits a unique porous architecture consisting of micrometer-sized clusters (secondary particles) composed of numerous nanoparticles (primary particles) and can be used directly without further carbon coating which is a common exercise for most electrode materials. The new anode displays superior cycling stability with a retained charge capacity of 725 mAh g(-1) after 300 cycles at 50 mA g(-1) . The electrode also offers excellent rate capability with a capacity recovery of 810 mAh g(-1) (94 % retention) after 35 cycles of ascending steps of current in the range of 25-800 mA g(-1) and finally back to 25 mA g(-1) . This work emphasizes the importance of exploring new electrode materials without carbon coating as carbon-coated materials demonstrate several drawbacks in full devices. Therefore, this study provides a method and a new type of anode with high reversibility and long cycle stability. © 2016 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  15. Strong Lithium Polysulfide Chemisorption on Electroactive Sites of Nitrogen-Doped Carbon Composites For High-Performance Lithium-Sulfur Battery Cathodes

    Energy Technology Data Exchange (ETDEWEB)

    Song, Jiangxuan [Pennsylvania State Univ., State College, PA (United States). Dept. of Mechanical and Nuclear Engineering; Gordin, Mikhail L. [Pennsylvania State Univ., State College, PA (United States). Dept. of Mechanical and Nuclear Engineering; Xu, Terrence [Pennsylvania State Univ., State College, PA (United States). Dept. of Mechanical and Nuclear Engineering; Chen, Shuru [Pennsylvania State Univ., State College, PA (United States). Dept. of Mechanical and Nuclear Engineering; Yu, Zhaoxin [Pennsylvania State Univ., State College, PA (United States). Dept. of Mechanical and Nuclear Engineering; Sohn, Hiesang [Pennsylvania State Univ., State College, PA (United States). Dept. of Mechanical and Nuclear Engineering; Lu, Jun [Argonne National Lab. (ANL), Argonne, IL (United States). Chemical Sciences and Engineering Div.; Ren, Yang [Argonne National Lab. (ANL), Argonne, IL (United States). X-ray Science Div.; Duan, Yuhua [National Energy Technology Lab. (NETL), Pittsburgh, PA, (United States); Wang, Donghai [Pennsylvania State Univ., State College, PA (United States). Dept. of Mechanical and Nuclear Engineering

    2015-03-27

    Despite the high theoretical capacity of lithium–sulfur batteries, their practical applications are severely hindered by a fast capacity decay, stemming from the dissolution and diffusion of lithium polysulfides in the electrolyte. A novel functional carbon composite (carbon-nanotube-interpenetrated mesoporous nitrogen-doped carbon spheres, MNCS/CNT), which can strongly adsorb lithium polysulfides, is now reported to act as a sulfur host. The nitrogen functional groups of this composite enable the effective trapping of lithium polysulfides on electroactive sites within the cathode, leading to a much improved electrochemical performance (1200 mAhg-1after 200 cycles). The enhancement in adsorption can be attributed to the chemical bonding of lithium ions by nitrogen functional groups in the MNCS/CNT framework. Furthermore, the micrometer-sized spherical structure of the material yields a high areal capacity (ca.6 mAhcm-2) with a high sulfur loading of approximately 5 mgcm-2, which is ideal for practical applications of the lithium–sulfur batteries.

  16. Nb2O5 microstructures: a high-performance anode for lithium ion batteries

    Science.gov (United States)

    Liu, Sainan; Zhou, Jiang; Cai, Zhenyang; Fang, Guozhao; Pan, Anqiang; Liang, Shuquan

    2016-11-01

    We report the synthesis of three-dimensional (3D) urchin-like Nb2O5 microstructures by a facile hydrothermal approach with subsequent annealing treatment. As anode materials for lithium-ion batteries, the 3D urchin-like Nb2O5 microstructures exhibit superior electrochemical performance with excellent rate capability as well as long-term cycling stability. The electrode delivers high capacity of 131 mA h g-1 after 1000 cycles at a high current density of 1 A g-1. The excellent electrochemical performance suggests the 3D urchin-like Nb2O5 microstructures may be a promising anode candidate for high-power lithium ion batteries.

  17. Fano resonance-based highly sensitive, compact temperature sensor on thin film lithium niobate.

    Science.gov (United States)

    Qiu, Wentao; Ndao, Abdoulaye; Vila, Venancio Calero; Salut, Roland; Courjal, Nadège; Baida, Fadi Issam; Bernal, Maria-Pilar

    2016-03-15

    In this Letter, we report a Fano resonance-based highly sensitive and compact temperature sensor fabricated on thin film lithium niobate (TFLN) Suzuki phase lattice (SPL) photonic crystal. The experimental sensitivity is estimated to be 0.77 nm/°C with a photonic crystal size of only 25  μm × 24  μm. This sensitivity is 38 times larger than the intrinsic one of lithium niobate which is 0.02 nm/°C. The demonstrated sharp and high extinction ratio characteristics of the Fano lineshape resonance could be an excellent candidate in developing a high sensitivity temperature sensor, electric field sensor, etc.

  18. High rate lithium-sulfur battery enabled by sandwiched single ion conducting polymer electrolyte

    Science.gov (United States)

    Sun, Yubao; Li, Gai; Lai, Yuanchu; Zeng, Danli; Cheng, Hansong

    2016-02-01

    Lithium-sulfur batteries are highly promising for electric energy storage with high energy density, abundant resources and low cost. However, the battery technologies have often suffered from a short cycle life and poor rate stability arising from the well-known “polysulfide shuttle” effect. Here, we report a novel cell design by sandwiching a sp3 boron based single ion conducting polymer electrolyte film between two carbon films to fabricate a composite separator for lithium-sulfur batteries. The dense negative charges uniformly distributed in the electrolyte membrane inherently prohibit transport of polysulfide anions formed in the cathode inside the polymer matrix and effectively blocks polysulfide shuttling. A battery assembled with the composite separator exhibits a remarkably long cycle life at high charge/discharge rates.

  19. Free-standing high quality factor thin-film lithium niobate micro-photonic disk resonators

    CERN Document Server

    Wang, Renyuan

    2014-01-01

    Lithium Niobate (LN or just niobate) thin-film micro-photonic resonators have promising prospects in many applications including high efficiency electro-optic modulators, optomechanics and nonlinear optics. This paper presents free-standing thin-film lithium niobate photonic resonators on a silicon platform using MEMS fabrication technology. We fabricated a 35um radius niobate disk resonator that exhibits high intrinsic optical quality factor (Q) of 484,000. Exploiting the optomechanical interaction from the released free-standing structure and high optical Q, we were able to demonstrate acousto-optic modulation from these devices by exciting a 56MHz radial breathing mechanical mode (mechanical Q of 2700) using a probe.

  20. FLUOLE-2: An Experiment for PWR Pressure Vessel Surveillance

    Directory of Open Access Journals (Sweden)

    Thiollay Nicolas

    2016-01-01

    Full Text Available FLUOLE-2 is a benchmark-type experiment dedicated to 900 and 1450 MWe PWR vessels surveillance dosimetry. This two-year program started in 2014 and will end in 2015. It will provide precise experimental data for the validation of the neutron spectrum propagation calculation from core to vessel. It is composed of a square core surrounded by a stainless steel baffe and internals: PWR barrel is simulated by steel structures leading to different steel-water slides; two steel components stand for a surveillance capsule holder and for a part of the pressure vessel. Measurement locations are available on the whole experimental structure. The experimental knowledge of core sources will be obtained by integral gamma scanning measurements directly on fuel pins. Reaction rates measured by calibrated fission chambers and a large set of dosimeters will give information on the neutron energy and spatial distributions. Due to the low level neutron flux of EOLE ZPR a special, high efficiency, calibrated gamma spectrometry device will be used for some dosimeters, allowing to measure an activity as low as 7. 10−2 Bq per sample. 103mRh activities will be measured on an absolute calibrated X spectrometry device. FLUOLE-2 experiment goal is to usefully complete the current experimental benchmarks database used for the validation of neutron calculation codes. This two-year program completes the initial FLUOLE program held in 2006–2007 in a geometry representative of 1300 MWe PWR.

  1. FLUOLE-2: An Experiment for PWR Pressure Vessel Surveillance

    Science.gov (United States)

    Thiollay, Nicolas; Di Salvo, Jacques; Sandrin, Charlotte; Soldevila, Michel; Bourganel, Stéphane; Fausser, Clément; Destouches, Christophe; Blaise, Patrick; Domergue, Christophe; Philibert, Hervé; Bonora, Jonathan; Gruel, Adrien; Geslot, Benoit; Lamirand, Vincent; Pepino, Alexandra; Roche, Alain; Méplan, Olivier; Ramdhane, Mourad

    2016-02-01

    FLUOLE-2 is a benchmark-type experiment dedicated to 900 and 1450 MWe PWR vessels surveillance dosimetry. This two-year program started in 2014 and will end in 2015. It will provide precise experimental data for the validation of the neutron spectrum propagation calculation from core to vessel. It is composed of a square core surrounded by a stainless steel baffe and internals: PWR barrel is simulated by steel structures leading to different steel-water slides; two steel components stand for a surveillance capsule holder and for a part of the pressure vessel. Measurement locations are available on the whole experimental structure. The experimental knowledge of core sources will be obtained by integral gamma scanning measurements directly on fuel pins. Reaction rates measured by calibrated fission chambers and a large set of dosimeters will give information on the neutron energy and spatial distributions. Due to the low level neutron flux of EOLE ZPR a special, high efficiency, calibrated gamma spectrometry device will be used for some dosimeters, allowing to measure an activity as low as 7. 10-2 Bq per sample. 103mRh activities will be measured on an absolute calibrated X spectrometry device. FLUOLE-2 experiment goal is to usefully complete the current experimental benchmarks database used for the validation of neutron calculation codes. This two-year program completes the initial FLUOLE program held in 2006-2007 in a geometry representative of 1300 MWe PWR.

  2. PWR core stablity aganst xenon-induced spatial power oscillation

    Energy Technology Data Exchange (ETDEWEB)

    Moon, H.J.; Han, K.I. (Korea Advanced Energy Research Inst., Seoul (Republic of Korea))

    1982-06-01

    Stability of a PWR core against xenon-induced axial power oscillation is studied using one-dimensional xenon transient analysis code, DD1D, that has been developed and verified at KAERI. Analyzed by DD1D utilizing the Kori Unit 1 design and operating data is the sensitivity of axial stability in a PWR core to the changes in core physical parameters including core power level, moderator temperature coefficient, core inlet temperature, doppler power coefficient and core average burnup. Through the sensitivity study the Kori Unit 1 core is found to be stable against axial xenon oscillation at the beginning of cycle 1. But, it becomes less stable as burnup progresses, and unstable at the end of cycle. Such a decrease in stability is mainly due to combined effect of changes in axial power distribution, moderator temperature coefficient and doppler power coefficient as core burnup progresses. It is concluded from the stability analysis of the Kori Unit 1 core that design of a large PWR with high power density and increased dimension can not avoid xenon-induced axial power instabilites to some extents, especially at the end of cycle.

  3. Study on novel functional materials carboxymethyl cellulose lithium (CMC-Li) improve high-performance lithium-ion battery.

    Science.gov (United States)

    Qiu, Lei; Shao, Ziqiang; Xiang, Pan; Wang, Daxiong; Zhou, Zhenwen; Wang, Feijun; Wang, Wenjun; Wang, Jianquan

    2014-09-22

    Novel cellulose derivative CMC-Li was synthesized by cotton as raw material. The mechanism of the CMC-Li modified electrode materials by electrospinning was reported. CMC-Li/lithium iron phosphate (LiFePO4, LFP) composite fiber coated with LFP and CMC-Li nanofibers was successfully obtained by electrospinning. Then, CMC-Li/LFP nano-composite fiber was carbonized under nitrogen at a high temperature formed CNF/LFP/Li (CLL) composite nanofibers as cathode material. It can increase the contents of Li+, and improving the diffusion efficiency and specific capacity. The battery with CLL as cathode material retained close to 100% of initial reversible capacity after 200 cycles at 168 mAh g(-1), which was nearly the theoretical specific capacity of LFP. The cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), X-ray diffraction (XRD) and scanning electron microscope (SEM) were characterizing material performance. The batteries have good electrochemical property, outstanding pollution-free, excellent stability. Copyright © 2014 Elsevier Ltd. All rights reserved.

  4. 4-(Trifluoromethyl)-benzonitrile: A novel electrolyte additive for lithium nickel manganese oxide cathode of high voltage lithium ion battery

    Science.gov (United States)

    Huang, Wenna; Xing, Lidan; Wang, Yating; Xu, Mengqing; Li, Weishan; Xie, Fengchao; Xia, Shengan

    2014-12-01

    In this work, 4-(Trifluoromethyl)-benzonitrile (4-TB) is used as a novel electrolyte additive for LiNi0.5Mn1.5O4 cathode of high voltage lithium ion battery. Charge-discharge tests show that the cyclic stability of LiNi0.5Mn1.5O4 is significantly improved by using 0.5 wt.% 4-TB. With using 4-TB, LiNi0.5Mn1.5O4 delivers an initial capacity of 133 mAh g-1 and maintains 121 mAh g-1 after 300 cycles with a capacity retention of 91%, compared to the 75% of that using base electrolyte (1 M LiPF6 in ethylene carbonate(EC)/dimethyl carbonate(DMC)). The results from linear sweep voltammetry, density functional theory calculations, electrochemical impedance spectroscopy, scanning electron microscope, energy dispersive spectroscopy, Fourier transform infrared, and inductively coupled plasma, indicate that 4-TB has lower oxidative stability than EC and DMC, and is preferentially oxidized on LiNi0.5Mn1.5O4 forming a low-impedance protective film, which prevents the subsequent oxidation decomposition of the electrolyte and suppresses the manganese dissolution from LiNi0.5Mn1.5O4.

  5. Diagnosis of power fade mechanisms in high-power lithium-ion cells

    Science.gov (United States)

    Abraham, D. P.; Liu, J.; Chen, C. H.; Hyung, Y. E.; Stoll, M.; Elsen, N.; MacLaren, S.; Twesten, R.; Haasch, R.; Sammann, E.; Petrov, I.; Amine, K.; Henriksen, G.

    Hybrid electric vehicles (HEV) need long-lived high-power batteries as energy storage devices. Batteries based on lithium-ion technology can meet the high-power goals but have been unable to meet HEV calendar-life requirements. As part of the US Department of Energy's Advanced Technology Development (ATD) Program, diagnostic studies are being conducted on 18650-type lithium-ion cells that were subjected to accelerated aging tests at temperatures ranging from 40 to 70 °C. This article summarizes data obtained by gas chromatography, liquid chromatography, electron microscopy, X-ray spectroscopy and electrochemical techniques, and identifies cell components that are responsible for the observed impedance rise and power fade.

  6. Identifying fade mechanisms in high-power lithium-ion cells.

    Energy Technology Data Exchange (ETDEWEB)

    Abraham, D. P.; Knuth, J.; Dees, D. W.; Jansen, A. N.; Sammann, E.; Haasch, R.; Twesten, R. D.; MacLaren, S.; Chemical Engineering; Univ. of Illinois

    2004-01-01

    Hybrid electric vehicles (HEV) need long-lived high-power batteries as energy storage devices. Batteries based on lithium-ion technology can meet the high-power goals but have been unable to meet HEV calendar-life requirements. As part of the US Department of Energy's Advanced Technology Development (ATD) Program, diagnostic studies are being conducted on 18650-type lithium-ion cells that were subjected to accelerated aging tests at temperatures ranging from 40 to 70 C. This article summarizes data obtained by gas chromatography, liquid chromatography, electron microscopy, X-ray spectroscopy and electrochemical techniques, and identifies cell components that are responsible for the observed impedance rise and power fade.

  7. High-capacity thick cathode with a porous aluminum current collector for lithium secondary batteries

    Science.gov (United States)

    Abe, Hidetoshi; Kubota, Masaaki; Nemoto, Miyu; Masuda, Yosuke; Tanaka, Yuichi; Munakata, Hirokazu; Kanamura, Kiyoshi

    2016-12-01

    A high-capacity thick cathode has been studied as one of ways to improve the energy density of lithium secondary batteries. In this study, the LiFePO4 cathode with a capacity per unit area of 8.4 m Ah cm-2 corresponding to four times the capacity of conventional cathodes has been developed using a three-dimensional porous aluminum current collector called "FUSPOROUS". This unique current collector enables the smooth transfer of electrons and Li+-ions through the thick cathode, resulting in a good rate capability (discharge capacity ratio of 1.0 C/0.2 C = 0.980) and a high charge-discharge cycle performance (80% of the initial capacity at 2000th cycle) even though the electrode thickness is 400 μm. To take practical advantage of the developed thick cathode, conceptual designs for a 10-Ah class cell were also carried out using graphite and lithium-metal anodes.

  8. Superconcentrated electrolytes for a high-voltage lithium-ion battery

    Science.gov (United States)

    Wang, Jianhui; Yamada, Yuki; Sodeyama, Keitaro; Chiang, Ching Hua; Tateyama, Yoshitaka; Yamada, Atsuo

    2016-01-01

    Finding a viable electrolyte for next-generation 5 V-class lithium-ion batteries is of primary importance. A long-standing obstacle has been metal-ion dissolution at high voltages. The LiPF6 salt in conventional electrolytes is chemically unstable, which accelerates transition metal dissolution of the electrode material, yet beneficially suppresses oxidative dissolution of the aluminium current collector; replacing LiPF6 with more stable lithium salts may diminish transition metal dissolution but unfortunately encounters severe aluminium oxidation. Here we report an electrolyte design that can solve this dilemma. By mixing a stable lithium salt LiN(SO2F)2 with dimethyl carbonate solvent at extremely high concentrations, we obtain an unusual liquid showing a three-dimensional network of anions and solvent molecules that coordinate strongly to Li+ ions. This simple formulation of superconcentrated LiN(SO2F)2/dimethyl carbonate electrolyte inhibits the dissolution of both aluminium and transition metal at around 5 V, and realizes a high-voltage LiNi0.5Mn1.5O4/graphite battery that exhibits excellent cycling durability, high rate capability and enhanced safety. PMID:27354162

  9. Superconcentrated electrolytes for a high-voltage lithium-ion battery

    Science.gov (United States)

    Wang, Jianhui; Yamada, Yuki; Sodeyama, Keitaro; Chiang, Ching Hua; Tateyama, Yoshitaka; Yamada, Atsuo

    2016-06-01

    Finding a viable electrolyte for next-generation 5 V-class lithium-ion batteries is of primary importance. A long-standing obstacle has been metal-ion dissolution at high voltages. The LiPF6 salt in conventional electrolytes is chemically unstable, which accelerates transition metal dissolution of the electrode material, yet beneficially suppresses oxidative dissolution of the aluminium current collector; replacing LiPF6 with more stable lithium salts may diminish transition metal dissolution but unfortunately encounters severe aluminium oxidation. Here we report an electrolyte design that can solve this dilemma. By mixing a stable lithium salt LiN(SO2F)2 with dimethyl carbonate solvent at extremely high concentrations, we obtain an unusual liquid showing a three-dimensional network of anions and solvent molecules that coordinate strongly to Li+ ions. This simple formulation of superconcentrated LiN(SO2F)2/dimethyl carbonate electrolyte inhibits the dissolution of both aluminium and transition metal at around 5 V, and realizes a high-voltage LiNi0.5Mn1.5O4/graphite battery that exhibits excellent cycling durability, high rate capability and enhanced safety.

  10. Interconnected Nanoflake Network Derived from a Natural Resource for High-Performance Lithium-Ion Batteries.

    Science.gov (United States)

    Cheng, Fei; Li, Wen-Cui; Lu, An-Hui

    2016-10-06

    Numerous natural resources have a highly interconnected network with developed porous structure, so enabling directional and fast matrix transport. Such structures are appealing for the design of efficient anode materials for lithium-ion batteries, although they can be challenging to prepare. Inspired by nature, a novel synthesis route from biomass is proposed by using readily available auricularia as retractable support and carbon coating precursor to soak up metal salt solution. Using the swelling properties of the auricularia with the complexation of metal ions, a nitrogen-containing MnO@C nanoflake network has been easily synthesized with fast electrochemical reaction dynamics and a superior lithium storage performance. A subsequent carbonization results in the in situ synthesis of MnO nanoparticles throughout the porous carbon flake network. When evaluated as an anode material for lithium-ion batteries, an excellent reversible capacity is achieved of 868 mA h g(-1) at 0.2 A g(-1) over 300 cycles and 668 mA h g(-1) at 1 A g(-1) over 500 cycles, indicating a high tolerance to the volume expansion. The approach investigated opens up new avenues for the design of high performance electrodes with highly cross-linked nanoflake structures, which may have great application prospects.

  11. Development of Nanoporous Carbide-Derived Carbon Electrodes for High-Performance Lithium-Ion Batteries

    Science.gov (United States)

    2011-09-01

    Advanced Energy Materials, vol. 22, pp. E28-E62, 2010. [2] D. Linden and T. B. Reddy, Handbook of Batteries , 3rd. New York: McGraw-Hill, 2002...Electrodes for High-Performance Lithium-Ion Batteries 5. FUNDING NUMBERS 6. AUTHOR( S ) Kamryn M. Sakamoto 7. PERFORMING ORGANIZATION NAME( S ) AND...5 accumulations, each at ~30 s ). 36 C. MACCOR BATTERY TESTER The button-type coin cells that were constructed were tested and cycled. The

  12. Conductive Polymer Binder-Enabled SiO-SnxCoyCz Anode for High-Energy Lithium-Ion Batteries.

    Science.gov (United States)

    Zhao, Hui; Fu, Yanbao; Ling, Min; Jia, Zhe; Song, Xiangyun; Chen, Zonghai; Lu, Jun; Amine, Khalil; Liu, Gao

    2016-06-01

    A SiOSnCoC composite anode is assembled using a conductive polymer binder for the application in next-generation high energy density lithium-ion batteries. A specific capacity of 700 mAh/g is achieved at a 1C (900 mA/g) rate. A high active material loading anode with an areal capacity of 3.5 mAh/cm(2) is demonstrated by mixing SiOSnCoC with graphite. To compensate for the lithium loss in the first cycle, stabilized lithium metal powder (SLMP) is used for prelithiation; when paired with a commercial cathode, a stable full cell cycling performance with a 86% first cycle efficiency is realized. By achieving these important metrics toward a practical application, this conductive polymer binder/SiOSnCoC anode system presents great promise to enable the next generation of high-energy lithium-ion batteries.

  13. Preparation of 3D nanoporous copper-supported cuprous oxide for high-performance lithium ion battery anodes.

    Science.gov (United States)

    Liu, Dequan; Yang, Zhibo; Wang, Peng; Li, Fei; Wang, Desheng; He, Deyan

    2013-03-01

    Three-dimensional (3D) nanoporous architectures can provide efficient and rapid pathways for Li-ion and electron transport as well as short solid-state diffusion lengths in lithium ion batteries (LIBs). In this work, 3D nanoporous copper-supported cuprous oxide was successfully fabricated by low-cost selective etching of an electron-beam melted Cu(50)Al(50) alloy and subsequent in situ thermal oxidation. The architecture was used as an anode in lithium ion batteries. In the first cycle, the sample delivered an extremely high lithium storage capacity of about 2.35 mA h cm(-2). A high reversible capacity of 1.45 mA h cm(-2) was achieved after 120 cycles. This work develops a promising approach to building reliable 3D nanostructured electrodes for high-performance lithium ion batteries.

  14. Application of Stabilized Lithium Metal Powder (SLMP®) in graphite anode - A high efficient prelithiation method for lithium-ion batteries

    Science.gov (United States)

    Wang, Zhihui; Fu, Yanbao; Zhang, Zhengcheng; Yuan, Shengwen; Amine, Khalil; Battaglia, Vincent; Liu, Gao

    2014-08-01

    Stabilized Lithium Metal Powder (SLMP®) was applied in graphite anode and the effects of this prelithiation method to cell performance were investigated. Performance of prelithiated cells was compared with that of regular graphite based cells. The first cycle capacity loss of SLMP prelithiated cell was largely reduced and the corresponding first cycle Coulombic efficiency was significantly improved. The graphite/NMC cell with SLMP prelithiation but without any standard cell formation process showed better cycle performance than that of none SLMP containing cell with standard formation process. Prelithiation of graphite electrode with SLMP promote stable solid electrolyte interface (SEI) formation on the surface of graphite anode. Application of SLMP in lithium-ion battery thus provides an effective method to enhance capacity, and promises a low cost SEI formation process. This also implies the potential use of other promising anode materials, such as Si and Sn that have large first cycle capacity loss, in commercial lithium-ion batteries.

  15. Lithium metal protection enabled by in-situ olefin polymerization for high-performance secondary lithium sulfur batteries

    Science.gov (United States)

    An, Yongling; Zhang, Zhen; Fei, Huifang; Xu, Xiaoyan; Xiong, Shenglin; Feng, Jinkui; Ci, Lijie

    2017-09-01

    Lithium metal is considered to be the optimal choice of next-generation anode materials due to its ultrahigh theoretical capacity and the lowest redox potential. However, the growth of dendritic and mossy lithium for rechargeable Li metal batteries lead to the possible short circuiting and subsequently serious safety issues during charge/discharge cycles. For the further practical applications of Li anode, here we report a facile method for fabricating robust interfacial layer via in-situ olefin polymerization. The resulting polymer layer effectively suppresses the formation of Li dendrites and enables the long-term operation of Li metal batteries. Using Li-S cells as a test system, we also demonstrate an improved capacity retention with the protection of tetramethylethylene-polymer. Our results indicate that this method could be a promising strategy to tackle the intrinsic problems of lithium metal anodes and promote the development of Li metal batteries.

  16. Nanostructured titanium nitride as a novel cathode for high performance lithium/dissolved polysulfide batteries

    Science.gov (United States)

    Mosavati, Negar; Chitturi, Venkateswara Rao; Salley, Steven O.; Ng, K. Y. Simon

    2016-07-01

    Lithium-sulfur (Lisbnd S) batteries could potentially revolutionize the rechargeable battery market due to their high energy density and low cost. However, low active material utilization, electrode volumetric expansion and a high rate of capacity fade due to the dissolution of lithium polysulfide intermediates in the liquid electrolyte are the main challenges facing further Lisbnd S battery development. Here, we enhanced Lisbnd S batteries active material utilization and decreased the volumetric expansion by using the lithium/dissolved polysulfide configuration. Moreover, a novel class of cathode materials, Titanium Nitride (TiN), was developed for polysulfide conversion reactions. The surface chemical environment of the TiN has been investigated by X-ray photoelectron spectroscopy (XPS) analysis. The existence of Ssbnd Tisbnd N bonding at the cathode electrode surface was observed, which indicates the strong interactions between TiN and polysulfides. Therefore, the TiN electrode retains the sulfur species on the cathode surface, minimizing the active material and surface area loss and consequently, improves the capacity retention. The resultant cells demonstrated a high initial capacity of 1524 mAh g-1 and a good capacity retention for 100 cycles at a C/10 current rate.

  17. Development of a 300 Amp-hr high rate lithium thionyl chloride cell

    Science.gov (United States)

    Boyle, Gerard H.

    1991-01-01

    The development of a high-rate lithium thionyl chloride cylindrical cell with parallel plate electrodes is discussed. The development was divided into three phases: phase 1, a 150 Amp/hour low rate (1 mA/sq cm) design; phase 2, a 25 Amp/hour high rate (5 mA/sq cm) design; and phase 3, a 300 Amp/hour high rate (5 mA/sq cm) design. The basic design is the same for all three cells. The electrodes are perpendicular to the axis of the cylinder. Multiple electrodes are bussed up the side of the cylinder, 180 deg apart allowing excellent anode and cathode utilization. It is a lithium limited design with excess electrolyte. The cathode is Shawinigan or Gulf Acetylene black with no catalyst. The electrolyte is 1.8 Molar lithium tetrachloroaluminate (LiAlCl4) in thionyl chloride. All cell cases are 304L Stainless Steel with a BS&B burst disc.

  18. Toward Low-Cost, High-Energy Density, and High-Power Density Lithium-Ion Batteries

    Science.gov (United States)

    Li, Jianlin; Du, Zhijia; Ruther, Rose E.; AN, Seong Jin; David, Lamuel Abraham; Hays, Kevin; Wood, Marissa; Phillip, Nathan D.; Sheng, Yangping; Mao, Chengyu; Kalnaus, Sergiy; Daniel, Claus; Wood, David L.

    2017-06-01

    Reducing cost and increasing energy density are two barriers for widespread application of lithium-ion batteries in electric vehicles. Although the cost of electric vehicle batteries has been reduced by 70% from 2008 to 2015, the current battery pack cost (268/kWh in 2015) is still >2 times what the USABC targets (125/kWh). Even though many advancements in cell chemistry have been realized since the lithium-ion battery was first commercialized in 1991, few major breakthroughs have occurred in the past decade. Therefore, future cost reduction will rely on cell manufacturing and broader market acceptance. This article discusses three major aspects for cost reduction: (1) quality control to minimize scrap rate in cell manufacturing; (2) novel electrode processing and engineering to reduce processing cost and increase energy density and throughputs; and (3) material development and optimization for lithium-ion batteries with high-energy density. Insights on increasing energy and power densities of lithium-ion batteries are also addressed.

  19. Toward Low-Cost, High-Energy Density, and High-Power Density Lithium-Ion Batteries

    Science.gov (United States)

    Li, Jianlin; Du, Zhijia; Ruther, Rose E.; AN, Seong Jin; David, Lamuel Abraham; Hays, Kevin; Wood, Marissa; Phillip, Nathan D.; Sheng, Yangping; Mao, Chengyu; Kalnaus, Sergiy; Daniel, Claus; Wood, David L.

    2017-09-01

    Reducing cost and increasing energy density are two barriers for widespread application of lithium-ion batteries in electric vehicles. Although the cost of electric vehicle batteries has been reduced by 70% from 2008 to 2015, the current battery pack cost (268/kWh in 2015) is still >2 times what the USABC targets (125/kWh). Even though many advancements in cell chemistry have been realized since the lithium-ion battery was first commercialized in 1991, few major breakthroughs have occurred in the past decade. Therefore, future cost reduction will rely on cell manufacturing and broader market acceptance. This article discusses three major aspects for cost reduction: (1) quality control to minimize scrap rate in cell manufacturing; (2) novel electrode processing and engineering to reduce processing cost and increase energy density and throughputs; and (3) material development and optimization for lithium-ion batteries with high-energy density. Insights on increasing energy and power densities of lithium-ion batteries are also addressed.

  20. Sandwich-like, graphene-based titania nanosheets with high surface area for fast lithium storage

    Energy Technology Data Exchange (ETDEWEB)

    Yang, Shubin; Feng, Xinliang; Muellen, Klaus [Max Planck Institute for Polymer Research, Mainz (Germany)

    2011-08-16

    Sandwich-like, graphene-based mesoporous titania (G-TiO{sub 2}) nanosheets possess thin thickness, large aspect ratio, and mesoporous structure and show enhanced electrical conductivity. Such unique features provide numerous open channels for the access of electrolyte and facilitate the fast diffusion of lithium ions during the cycling processes. The graphene layer within each nanosheet can act as a mini-current collector, which is favorable for the fast electron transport in the electrode. As a consequence, G-TiO{sub 2} nanosheets exhibit a ultrahigh rate capability and excellent cycle performance, holding great potential as a high-rate anode material for lithium storage. (Copyright copyright 2011 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  1. Sparingly Solvating Electrolytes for High Energy Density Lithium-Sulfur Batteries

    Energy Technology Data Exchange (ETDEWEB)

    Cheng, Lei; Curtiss, Larry A.; Zavadil, Kevin R.; Gewirth, Andrew A.; Shao, Yuyan; Gallagher, Kevin

    2016-07-11

    Moving to lighter and less expensive battery chemistries compared to lithium-ion requires the control of energy storage mechanisms based on chemical transformations rather than intercalation. Lithium sulfur (Li/S) has tremendous theoretical specific energy, but contemporary approaches to control this solution-mediated, precipitation-dissolution chemistry requires using large excesses of electrolyte to fully solubilize the polysulfide intermediate. Achieving reversible electrochemistry under lean electrolyte operation is the only path for Li/S to move beyond niche applications to potentially transformational performance. An emerging topic for Li/S research is the use of sparingly solvating electrolytes and the creation of design rules for discovering new electrolyte systems that fundamentally decouple electrolyte volume from reaction mechanism. This perspective presents an outlook for sparingly solvating electrolytes as the key path forward for longer-lived, high-energy density Li/S batteries including an overview of this promising new concept and some strategies for accomplishing it.

  2. Biomass Waste Inspired Highly Porous Carbon for High Performance Lithium/Sulfur Batteries.

    Science.gov (United States)

    Zhao, Yan; Ren, Jun; Tan, Taizhe; Babaa, Moulay-Rachid; Bakenov, Zhumabay; Liu, Ning; Zhang, Yongguang

    2017-09-06

    The synthesis of highly porous carbon (HPC) materials from poplar catkin by KOH chemical activation and hydrothermal carbonization as a conductive additive to a lithium-sulfur cathode is reported. Elemental sulfur was composited with as-prepared HPC through a melt diffusion method to form a S/HPC nanocomposite. Structure and morphology characterization revealed a hierarchically sponge-like structure of HPC with high pore volume (0.62 cm³∙g (−1) ) and large specific surface area (1261.7 m²∙g (−1) ). When tested in Li/S batteries, the resulting compound demonstrated excellent cycling stability, delivering a second-specific capacity of 1154 mAh∙g (−1) as well as presenting 74% retention of value after 100 cycles at 0.1 C. Therefore, the porous structure of HPC plays an important role in enhancing electrochemical properties, which provides conditions for effective charge transfer and effective trapping of soluble polysulfide intermediates, and remarkably improves the electrochemical performance of S/HPC composite cathodes.

  3. Highly Conductive Solvent-Free Polymer Electrolytes for Lithium Rechargeable Batteries

    Energy Technology Data Exchange (ETDEWEB)

    Robert Filler, Zhong Shi and Braja Mandal

    2004-10-21

    In order to obviate the deficiencies of currently used electrolytes in lithium rechargeable batteries, there is a compelling need for the development of solvent-free, highly conducting solid polymer electrolytes (SPEs). The problem will be addressed by synthesizing a new class of block copolymers and plasticizers, which will be used in the formulation of highly conducting electrolytes for lithium-ion batteries. The main objective of this Phase-I effort is to determine the efficacy and commercial prospects of new specifically designed SPEs for use in electric and hybrid electric vehicle (EV/HEV) batteries. This goal will be achieved by preparing the SPEs on a small scale with thorough analyses of their physical, chemical, thermal, mechanical and electrochemical properties. SPEs will play a key role in the formulation of next generation lithium-ion batteries and will have a major impact on the future development of EVs/HEVs and a broad range of consumer products, e.g., computers, camcorders, cell phones, cameras, and power tools.

  4. High Lithium Transference Number Electrolytes via Creation of 3-Dimensional, Charged, Nanoporous Networks from Dense Functionalized Nanoparticle Composites

    KAUST Repository

    Schaefer, Jennifer L.

    2013-03-26

    High lithium transference number, tLi+, electrolytes are desired for use in both lithium-ion and lithium metal rechargeable battery technologies. Historically, low tLi+ electrolytes have hindered device performance by allowing ion concentration gradients within the cell, leading to high internal resistances that ultimately limit cell lifetime, charging rates, and energy density. Herein, we report on the synthesis and electrochemical features of electrolytes based on nanoparticle salts designed to provide high tLi+. The salts are created by cofunctionalization of metal oxide nanoparticles with neutral organic ligands and tethered lithium salts. When dispersed in a conducting fluid such as tetraglyme, they spontaneously form a charged, nanoporous network of particles at moderate nanoparticle loadings. Modification of the tethered anion chemistry from -SO3 - to -SO3BF3 - is shown to enhance ionic conductivity of the electrolytes by facilitating ion pair dissociation. At a particle volume fraction of 0.15, the electrolyte exists as a self-supported, nanoporous gel with an optimum ionic conductivity of 10 -4 S/cm at room temperature. Galvanostatic polarization measurements on symmetric lithium metal cells containing the electrolyte show that the cell short circuit time, tSC, is inversely proportional to the square of the applied current density tSC ∼ J-2, consistent with previously predicted results for traditional polymer-in-salt electrolytes with low tLi+. Our findings suggest that electrolytes with tLi+ ≈ 1 and good ion-pair dissociation delay lithium dendrite nucleation and may lead to improved lithium plating in rechargeable batteries with metallic lithium anodes. © 2013 American Chemical Society.

  5. High rate lithium batteries safety testing for U.L. component recognition

    Science.gov (United States)

    Snuggerud, D. K.

    1985-12-01

    An evaluation is made of the safety-related aspects of high energy density lithium thionyl chloride batteries by subjecting them to extensive testing in that system configuration that has the highest hazard potential in virtue of its high voltage. The molten Li (at above 180 C) is violently reactive with the battery cathode material. Attention is given to designs which fuse current collectors to the Li at high heat values, and especially to a design that limits the movement of molten Li and thereby prevents internal short circuits. Results of safety tests concerned with battery operation in military applications are also noted.

  6. Hierarchically structured lithium titanate for ultrafast charging in long-life high capacity batteries

    Science.gov (United States)

    Odziomek, Mateusz; Chaput, Frédéric; Rutkowska, Anna; Świerczek, Konrad; Olszewska, Danuta; Sitarz, Maciej; Lerouge, Frédéric; Parola, Stephane

    2017-05-01

    High-performance Li-ion batteries require materials with well-designed and controlled structures on nanometre and micrometre scales. Electrochemical properties can be enhanced by reducing crystallite size and by manipulating structure and morphology. Here we show a method for preparing hierarchically structured Li4Ti5O12 yielding nano- and microstructure well-suited for use in lithium-ion batteries. Scalable glycothermal synthesis yields well-crystallized primary 4-8 nm nanoparticles, assembled into porous secondary particles. X-ray photoelectron spectroscopy reveals presence of Ti+4 only; combined with chemical analysis showing lithium deficiency, this suggests oxygen non-stoichiometry. Electron microscopy confirms hierarchical morphology of the obtained material. Extended cycling tests in half cells demonstrates capacity of 170 mAh g-1 and no sign of capacity fading after 1,000 cycles at 50C rate (charging completed in 72 s). The particular combination of nanostructure, microstructure and non-stoichiometry for the prepared lithium titanate is believed to underlie the observed electrochemical performance of material.

  7. Mixed Electronic and Ionic Conductor-Coated Cathode Material for High-Voltage Lithium Ion Battery.

    Science.gov (United States)

    Shim, Jae-Hyun; Han, Jung-Min; Lee, Joon-Hyung; Lee, Sanghun

    2016-05-18

    A lithium ionic conductor, Li1.3Al0.3Ti1.7(PO4)3 (LATP), is introduced as a coating material on the surface of Mg-doped LiCoO2 to improve electrochemical performances for high-voltage (4.5 V) lithium ion batteries. Structure, morphology, elemental distribution, and electrical properties of the materials are thoroughly characterized by SEM, TEM, EELS, EDS, and C-AFM. The coating layer is electrically conductive with the aid of Mg ions which are used as a dopant for the active materials; therefore, this mixed electronic ionic conductor strongly enhances the electrochemical performances of initial capacity, cycling property, and rate capability. The LATP coating layer also demonstrates very promising applicability for 4.4 V prismatic full cells with graphite anode, which correspond to the 4.5 V half-cells with lithium anode. The 2900 mA h full cells show 85% of capacity retention after 500 cycles and more than 60% after 700 cycles.

  8. A PWR Thorium Pin Cell Burnup Benchmark

    Energy Technology Data Exchange (ETDEWEB)

    Weaver, Kevan Dean; Zhao, X.; Pilat, E. E; Hejzlar, P.

    2000-05-01

    As part of work to evaluate the potential benefits of using thorium in LWR fuel, a thorium fueled benchmark comparison was made in this study between state-of-the-art codes, MOCUP (MCNP4B + ORIGEN2), and CASMO-4 for burnup calculations. The MOCUP runs were done individually at MIT and INEEL, using the same model but with some differences in techniques and cross section libraries. Eigenvalue and isotope concentrations were compared on a PWR pin cell model up to high burnup. The eigenvalue comparison as a function of burnup is good: the maximum difference is within 2% and the average absolute difference less than 1%. The isotope concentration comparisons are better than a set of MOX fuel benchmarks and comparable to a set of uranium fuel benchmarks reported in the literature. The actinide and fission product data sources used in the MOCUP burnup calculations for a typical thorium fuel are documented. Reasons for code vs code differences are analyzed and discussed.

  9. Conceptual study of advanced PWR core design

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Young Jin; Chang, Moon Hee; Kim, Keung Ku; Joo, Hyung Kuk; Kim, Young Il; Noh, Jae Man; Hwang, Dae Hyun; Kim, Taek Kyum; Yoo, Yon Jong

    1997-09-01

    The purpose of this project is for developing and verifying the core design concepts with enhanced safety and economy, and associated methodologies for core analyses. From the study of the sate-of-art of foreign advanced reactor cores, we developed core concepts such as soluble boron free, high convertible and enhanced safety core loaded semi-tight lattice hexagonal fuel assemblies. To analyze this hexagonal core, we have developed and verified some neutronic and T/H analysis methodologies. HELIOS code was adopted as the assembly code and HEXFEM code was developed for hexagonal core analysis. Based on experimental data in hexagonal lattices and the COBRA-IV-I code, we developed a thermal-hydraulic analysis code for hexagonal lattices. Using the core analysis code systems developed in this project, we designed a 600 MWe core and studied the feasibility of the core concepts. Two additional scopes were performed in this project : study on the operational strategies of soluble boron free core and conceptual design of large scale passive core. By using the axial BP zoning concept and suitable design of control rods, this project showed that it was possible to design a soluble boron free core in 600 MWe PWR. The results of large scale core design showed that passive concepts and daily load follow operation could be practiced. (author). 15 refs., 52 tabs., 101 figs.

  10. Taichi-inspired rigid-flexible coupling cellulose-supported solid polymer electrolyte for high-performance lithium batteries.

    Science.gov (United States)

    Zhang, Jianjun; Yue, Liping; Hu, Pu; Liu, Zhihong; Qin, Bingsheng; Zhang, Bo; Wang, Qingfu; Ding, Guoliang; Zhang, Chuanjian; Zhou, Xinhong; Yao, Jianhua; Cui, Guanglei; Chen, Liquan

    2014-09-03

    Inspired by Taichi, we proposed rigid-flexible coupling concept and herein developed a highly promising solid polymer electrolyte comprised of poly (ethylene oxide), poly (cyano acrylate), lithium bis(oxalate)borate and robust cellulose nonwoven. Our investigation revealed that this new class solid polymer electrolyte possessed comprehensive properties in high mechanical integrity strength, sufficient ionic conductivity (3 × 10(-4) S cm(-1)) at 60°C and improved dimensional thermostability (up to 160°C). In addition, the lithium iron phosphate (LiFePO4)/lithium (Li) cell using such solid polymer electrolyte displayed superior rate capacity (up to 6 C) and stable cycle performance at 80°C. Furthermore, the LiFePO4/Li battery could also operate very well even at an elevated temperature of 160°C, thus improving enhanced safety performance of lithium batteries. The use of this solid polymer electrolyte mitigates the safety risk and widens the operation temperature range of lithium batteries. Thus, this fascinating study demonstrates a proof of concept of the use of rigid-flexible coupling solid polymer electrolyte toward practical lithium battery applications with improved reliability and safety.

  11. A binder-free sulfur/reduced graphene oxide aerogel as high performance electrode materials for lithium sulfur batteries

    Science.gov (United States)

    Nitze, Florian; Agostini, Marco; Lundin, Filippa; Palmqvist, Anders E. C.; Matic, Aleksandar

    2016-12-01

    Societies’ increasing need for energy storage makes it necessary to explore new concepts beyond the traditional lithium ion battery. A promising candidate is the lithium-sulfur technology with the potential to increase the energy density of the battery by a factor of 3-5. However, so far the many problems with the lithium-sulfur system have not been solved satisfactory. Here we report on a new approach utilizing a self-standing reduced graphene oxide based aerogel directly as electrodes, i.e. without further processing and without the addition of binder or conducting agents. We can thereby disrupt the common paradigm of “no battery without binder” and can pave the way to a lithium-sulfur battery with a high practical energy density. The aerogels are synthesized via a one-pot method and consist of more than 2/3 sulfur, contained inside a porous few-layered reduced graphene oxide matrix. By combining the graphene-based aerogel cathode with an electrolyte and a lithium metal anode, we demonstrate a lithium-sulfur cell with high areal capacity (more than 3 mAh/cm2 after 75 cycles), excellent capacity retention over 200 cycles and good sulfur utilization. Based on this performance we estimate that the energy density of this concept-cell can significantly exceed the Department of Energy (DEO) 2020-target set for transport applications.

  12. High Energy Density Lithium Air Batteries for Oxygen Concentrators Project

    Data.gov (United States)

    National Aeronautics and Space Administration — For NASA's Exploration Medical Capabilities mission, extremely high specific energy power sources, with specific energy over 2000 Wh/kg, are urgently sought after....

  13. Band structure and phonon properties of lithium fluoride at high pressure

    Energy Technology Data Exchange (ETDEWEB)

    Panchal, J. M., E-mail: amitjignesh@yahoo.co.in [Government Engineering College, Gandhinagar 382028, Gujarat (India); Department of Physics, University School of Sciences, Gujarat University, Ahmedabad 380009, Gujarat (India); Joshi, Mitesh [Government Polytechnic for Girls, Athwagate, Surat395001, Gujarat (India); Gajjar, P. N., E-mail: pngajjar@rediffmail.com [Department of Physics, University School of Sciences, Gujarat University, Ahmedabad 380009, Gujarat (India)

    2016-05-23

    High pressure structural and electronic properties of Lithium Fluoride (LiF) have been studied by employing an ab-initio pseudopotential method and a linear response scheme within the density functional theory (DFT) in conjunction with quasi harmonic Debye model. The band structure and electronic density of states conforms that the LiF is stable and is having insulator behavior at ambient as well as at high pressure up to 1 Mbar. Conclusions based on Band structure, phonon dispersion and phonon density of states are outlined.

  14. Toward the design of high voltage magnesium–lithium hybrid batteries using dual-salt electrolytes

    Energy Technology Data Exchange (ETDEWEB)

    Cheng, Yingwen; Choi, Daiwon; Han, Kee Sung; Mueller, Karl T.; Zhang, Ji-Guang; Sprenkle, Vincent L.; Liu, Jun; Li, Guosheng

    2016-02-26

    We report a design of high voltage magnesium-lithium (Mg-Li) hybrid batteries through rational controls of the electrolyte chemistry, electrode materials and cell architectures. Prototype devices with LiFePO4 and LiMn2O4 cathodes exhibit voltages higher than 2.5 V (vs. Mg) and a high specific energy density of 246 Wh/kg under conditions that are amenable for practical applications. The successful demonstrations reported here could be a significant step forward for practical hybrid batteries.

  15. A high performance silicon/carbon composite anode with carbon nanofiber for lithium-ion batteries

    Science.gov (United States)

    Si, Q.; Hanai, K.; Ichikawa, T.; Hirano, A.; Imanishi, N.; Takeda, Y.; Yamamoto, O.

    The electrochemical performance of a composite of nano-Si powder and a pyrolytic carbon of polyvinyl chloride (PVC) with carbon nanofiber (CNF) was examined as an anode for lithium-ion batteries. CNF was incorporated into the composite by two methods; direct mixing of CNF with the nano-Si powder coated with carbon produced by pyrolysis of PVC (referred to as Si/C/CNF-1) and mixing of CNF, nano-Si powder, and PVC with subsequent firing (referred to as Si/C/CNF-2). The external Brunauer-Emmett-Teller (BET) surface area of Si/C/CNF-1 was comparable to that of Si/C/CNF-2. The micropore BET surface area of Si/C/CNF-2 (73.86 m 2 g -1) was extremely higher than that of Si/C/CNF-1 (0.74 m 2 g -1). The composites prepared by both methods exhibited high capacity and excellent cycling stability for lithium insertion and extraction. A capacity of more than 900 mA h g -1 was maintained after 30 cycles. The coulombic efficiency of the first cycle for Si/C/CNF-1 was as low as 53%, compared with 73% for Si/C/CNF-2. Impedance analysis of cells containing these anode materials suggested that the charge transfer resistance for Si/C/CNF-1 was not changed by cycling, but that Si/C/CNF-2 had high charge transfer resistance after cycling. A composite electrode prepared by mixing Si/C/CNF-2 and CNF exhibited a high reversible capacity at high rate, excellent cycling performance, and a high coulombic efficiency during the first lithium insertion and extraction cycles.

  16. Synthesis of high-quality mesoporous silicon particles for enhanced lithium storage performance

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Chundong, E-mail: apcdwang@hust.edu.cn [School of Optical and Electronic Information, Huazhong University of Science and Technology, Wuhan 430074 (China); Center of Super-Diamond and Advanced Films (COSDAF), Department of Physics and Materials Science, City University of Hong Kong, Kowloon, Hong Kong SAR (China); Ren, Jianguo [Center of Super-Diamond and Advanced Films (COSDAF), Department of Physics and Materials Science, City University of Hong Kong, Kowloon, Hong Kong SAR (China); Chen, Hao [Department of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou (China); Zhang, Yi [School of Chemical Engineering and Pharmacy, Wuhan Institute of Technology, Wuhan, 430073 (China); Ostrikov, Kostya [School of Chemistry, Physics, and Mechanical Engineering, Queensland University of Technology, Brisbane 4000, QLD (Australia); Manufacturing Flagship, CSIRO, P. O. Box 218, Lindfield, NSW 2070 (Australia); Zhang, Wenjun [Center of Super-Diamond and Advanced Films (COSDAF), Department of Physics and Materials Science, City University of Hong Kong, Kowloon, Hong Kong SAR (China); Li, Yi, E-mail: liyi@suda.edu.cn [Department of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou (China); Center of Super-Diamond and Advanced Films (COSDAF), Department of Physics and Materials Science, City University of Hong Kong, Kowloon, Hong Kong SAR (China)

    2016-04-15

    Silicon has been considered as one of the most promising anode materials for high-capacity lithium-ion batteries (LIBs) due to its ultrahigh theoretical capacity, abundance, and environmentally benign nature. Nonetheless, the severe break during the prolonged cycling results in poor electrochemical performance, which hinders its practical application. Herein, we report the synthesis of novel mesoporous silicon particles with a facile template method by using a magnesiothermic reduction for LIBs. The obtained silicon nanoparticles are highly porous with densely porous cavities (20–40 nm) on the wall, of which it presents good crystallization. Electrochemical measurements showed that the mesoporous silicon nanoparticles delivered a high reversible specific capacity of 910 mA h g{sup −1} at a high current density of 1200 mA g{sup −1} over 50 cycles. The specific capacity at such high current density is still over twofold than that of commercial graphite anode, suggesting that the nanoporous Si architectures is suitable for high-performance Si-based anodes for lithium ion batteries in terms of capacity, cycle life, and rate capacity. - Highlights: • Silica nanotubes were prepared with a facile template method. • Novel mesoporous silicon particles were obtained by magnesiothermic reduction. • High-Performance LIBs were achieved by using mesoporous Si particle Electrodes.

  17. High Capacity Nano-Composite Cathodes for Human-Rated Lithium-Ion Batteries Project

    Data.gov (United States)

    National Aeronautics and Space Administration — Non-incremental improvements are necessary in lithium-ion batteries order to meet future space applications demands such as NASA's call for lithium-ion battery...

  18. Laser beam welding of high strength aluminium-lithium alloys; Laserstrahlschweissen von hochfesten Aluminium-Lithium Legierungen

    Energy Technology Data Exchange (ETDEWEB)

    Enz, Josephin

    2012-07-01

    The present development in aircraft industry determined by the demand for a higher cost-effectiveness. Laser beam welding is one of the most promising joining technologies for the application in the aircraft industry through the considerable reduction of the production costs. Furthermore the weight of an aircraft structure can be reduced by the use of light and high strength aluminium alloys. This paper deals with the development of a process for the laser beam welding of a skin-stringer-joint where the Al-Li-alloy AA2196 is used as stringer material and the Al-Li-alloy AA2198 is used as skin and stringer material. By the use of design of experiments the optimal welding process parameters for different material combinations were determined which will be used for the welding of a 5-stringer panel. Therefore the weld seams of the joints were tested for irregularities and microstructural characteristics. In addition several mechanical tests were performed, which define the quality of the welded joint. Furthermore the influence of the oxide layer and the welding preparation on the welding performance was investigated. (orig.) [German] Die derzeitigen Entwicklungen im Flugzeugbau werden durch die allgemeine Forderung nach einer Steigerung der Wirtschaftlichkeit bestimmt. Das Laserstrahlschweissen ist dabei eines der vielversprechendsten Fuegeverfahren fuer die Anwendung im Flugzeugbau durch das die Herstellungskosten deutlich reduziert werden koennen. Zudem kann durch die Verwendung von leichten und hochfesten Aluminium-Legierungen das Gewicht einer Flugzeugstruktur zusaetzlich reduziert werden. Die vorliegende Arbeit befasst sich mit der Entwicklung eines Prozesses zum Laserstrahlschweissen einer Skin-Stringer-Verbindung aus den Aluminium-Lithium-Legierungen AA2196 (als Stringer-Werkstoff) und AA2198 (als Skin- und Stringer-Werkstoff). Unter Verwendung der statistischen Versuchsplanung wurden die optimalen Einstellungen der Schweissprozessparameter fuer die

  19. A high conductivity oxide–sulfide composite lithium superionic conductor

    Energy Technology Data Exchange (ETDEWEB)

    Rangasamy, Ezhiylmurugan [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States). Center for Nanophase Materials Science; Sahu, Gayatri [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States). Center for Nanophase Materials Science; Keum, Jong Kahk [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States). Center for Nanophase Materials Science; Rondinone, Adam J. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States). Center for Nanophase Materials Science; Dudney, Nancy J. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States). Materials Science and Technology Division; Liang, Chengdu [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States). Center for Nanophase Materials Science

    2014-01-14

    We fabricated a hybrid superionic conductor using the space charge effect between the LLZO and LPS interfaces. This space-charge effect resulted in an improvement over the individual bulk conductivities of the two systems. Sample with higher weight fractions of LLZO are limited by the porosity and grain boundary resistance arising from non-sintered membranes. Furthermore, by combining the properties of LLZO and LPS, the high temperature sintering step has been avoided thus facilitating easier materials processing. The interfacial resistances were also measured to be minimal at ambient conditions. Our procedure thus opens a new avenue for improving the ionic conductivity and electrochemical properties of existing solid state electrolytes. High frequency impedance analyses could aid in resolving the ionic conductivity contributions from the space charge layer in the higher conducting composites while mechanical property investigations could illustrate an improvement in the composite electrolyte in comparison with the crystalline LPS membranes.

  20. Lithium use in batteries

    Science.gov (United States)

    Goonan, Thomas G.

    2012-01-01

    Lithium has a number of uses but one of the most valuable is as a component of high energy-density rechargeable lithium-ion batteries. Because of concerns over carbon dioxide footprint and increasing hydrocarbon fuel cost (reduced supply), lithium may become even more important in large batteries for powering all-electric and hybrid vehicles. It would take 1.4 to 3.0 kilograms of lithium equivalent (7.5 to 16.0 kilograms of lithium carbonate) to support a 40-mile trip in an electric vehicle before requiring recharge. This could create a large demand for lithium. Estimates of future lithium demand vary, based on numerous variables. Some of those variables include the potential for recycling, widespread public acceptance of electric vehicles, or the possibility of incentives for converting to lithium-ion-powered engines. Increased electric usage could cause electricity prices to increase. Because of reduced demand, hydrocarbon fuel prices would likely decrease, making hydrocarbon fuel more desirable. In 2009, 13 percent of worldwide lithium reserves, expressed in terms of contained lithium, were reported to be within hard rock mineral deposits, and 87 percent, within brine deposits. Most of the lithium recovered from brine came from Chile, with smaller amounts from China, Argentina, and the United States. Chile also has lithium mineral reserves, as does Australia. Another source of lithium is from recycled batteries. When lithium-ion batteries begin to power vehicles, it is expected that battery recycling rates will increase because vehicle battery recycling systems can be used to produce new lithium-ion batteries.

  1. Fibrous hybrid of graphene and sulfur nanocrystals for high-performance lithium-sulfur batteries.

    Science.gov (United States)

    Zhou, Guangmin; Yin, Li-Chang; Wang, Da-Wei; Li, Lu; Pei, Songfeng; Gentle, Ian Ross; Li, Feng; Cheng, Hui-Ming

    2013-06-25

    Graphene-sulfur (G-S) hybrid materials with sulfur nanocrystals anchored on interconnected fibrous graphene are obtained by a facile one-pot strategy using a sulfur/carbon disulfide/alcohol mixed solution. The reduction of graphene oxide and the formation/binding of sulfur nanocrystals were integrated. The G-S hybrids exhibit a highly porous network structure constructed by fibrous graphene, many electrically conducting pathways, and easily tunable sulfur content, which can be cut and pressed into pellets to be directly used as lithium-sulfur battery cathodes without using a metal current-collector, binder, and conductive additive. The porous network and sulfur nanocrystals enable rapid ion transport and short Li(+) diffusion distance, the interconnected fibrous graphene provides highly conductive electron transport pathways, and the oxygen-containing (mainly hydroxyl/epoxide) groups show strong binding with polysulfides, preventing their dissolution into the electrolyte based on first-principles calculations. As a result, the G-S hybrids show a high capacity, an excellent high-rate performance, and a long life over 100 cycles. These results demonstrate the great potential of this unique hybrid structure as cathodes for high-performance lithium-sulfur batteries.

  2. Hollow Carbon Nanofiber-Encapsulated Sulfur Cathodes for High Specific Capacity Rechargeable Lithium Batteries

    KAUST Repository

    Zheng, Guangyuan

    2011-10-12

    Sulfur has a high specific capacity of 1673 mAh/g as lithium battery cathodes, but its rapid capacity fading due to polysulfides dissolution presents a significant challenge for practical applications. Here we report a hollow carbon nanofiber-encapsulated sulfur cathode for effective trapping of polysulfides and demonstrate experimentally high specific capacity and excellent electrochemical cycling of the cells. The hollow carbon nanofiber arrays were fabricated using anodic aluminum oxide (AAO) templates, through thermal carbonization of polystyrene. The AAO template also facilitates sulfur infusion into the hollow fibers and prevents sulfur from coating onto the exterior carbon wall. The high aspect ratio of the carbon nanofibers provides an ideal structure for trapping polysulfides, and the thin carbon wall allows rapid transport of lithium ions. The small dimension of these nanofibers provides a large surface area per unit mass for Li2S deposition during cycling and reduces pulverization of electrode materials due to volumetric expansion. A high specific capacity of about 730 mAh/g was observed at C/5 rate after 150 cycles of charge/discharge. The introduction of LiNO3 additive to the electrolyte was shown to improve the Coulombic efficiency to over 99% at C/5. The results show that the hollow carbon nanofiber-encapsulated sulfur structure could be a promising cathode design for rechargeable Li/S batteries with high specific energy. © 2011 American Chemical Society.

  3. Nonlinear Fuzzy Model Predictive Control for a PWR Nuclear Power Plant

    Directory of Open Access Journals (Sweden)

    Xiangjie Liu

    2014-01-01

    Full Text Available Reliable power and temperature control in pressurized water reactor (PWR nuclear power plant is necessary to guarantee high efficiency and plant safety. Since the nuclear plants are quite nonlinear, the paper presents nonlinear fuzzy model predictive control (MPC, by incorporating the realistic constraints, to realize the plant optimization. T-S fuzzy modeling on nuclear power plant is utilized to approximate the nonlinear plant, based on which the nonlinear MPC controller is devised via parallel distributed compensation (PDC scheme in order to solve the nonlinear constraint optimization problem. Improved performance compared to the traditional PID controller for a TMI-type PWR is obtained in the simulation.

  4. AREVA solutions to licensing challenges in PWR and BWR reload and safety analysis

    Energy Technology Data Exchange (ETDEWEB)

    Curca-Tivig, Florin [AREVA GmbH, Erlangen (Germany)

    2016-05-15

    Regulatory requirements for reload and safety analyses are evolving: new safety criteria, request for enlarged qualification databases, statistical applications, uncertainty propagation.. In order to address these challenges and access more predictable licensing processes, AVERA is implementing consistent code and methodology suites for PWR and BWR core design and safety analysis, based on first principles modeling and extremely broad verification and validation data base. Thanks to the high computational power increase in the last decades methods' development and application now include new capabilities. An overview of the main AREVA codes and methods developments is given covering PWR and BWR applications in different licensing environments.

  5. Synthesis and electrospinning carboxymethyl cellulose lithium (CMC-Li) modified 9,10-anthraquinone (AQ) high-rate lithium-ion battery.

    Science.gov (United States)

    Qiu, Lei; Shao, Ziqiang; Liu, Minglong; Wang, Jianquan; Li, Pengfa; Zhao, Ming

    2014-02-15

    New cellulose derivative CMC-Li was synthesized, and nanometer CMC-Li fiber was applied to lithium-ion battery and coated with AQ by electrospinning. Under the protection of inert gas, modified AQ/carbon nanofibers (CNF)/Li nanometer composite material was obtained by carbonization in 280 °C as lithium battery anode materials for the first time. The morphologies and structures performance of materials were characterized by using IR, (1)H NMR, SEM, CV and EIS, respectively. Specific capacity was increased from 197 to 226.4 mAhg(-1) after modification for the first discharge at the rate of 2C. Irreversible reduction reaction peaks of modified material appeared between 1.5 and 1.7 V and the lowest oxidation reduction peak of the difference were 0.42 V, the polarization was weaker. Performance of cell with CMC-Li with the high degree of substitution (DS) was superior to that with low DS. Cellulose materials were applied to lithium battery to improve battery performance by electrospinning. Copyright © 2013 Elsevier Ltd. All rights reserved.

  6. High temperature flow behaviour of SiC reinforced lithium aluminosilicate composites

    Indian Academy of Sciences (India)

    Santanu Das; V S R Murthy; G S Murty

    2001-04-01

    The compressive flow behaviour of lithium aluminosilicate (LAS) glass, with and without SiC particulate reinforcements, was studied. The LAS glass crystallized to spodumene during high-temperature testing. The flow behaviour of LAS glass changed from Newtonian to non-Newtonian due to the presence of crystalline phase. Further, with the addition of 40 vol.% SiC additions, the strain rate sensitivity of flow stress decreased. While the activation energy for flow in LAS was 300 kJ/mole, it increased to 995 kJ/mole with the addition of 40 vol.% SiC reinforcements.

  7. High resolution x-ray investigation of periodically poled lithium tantalate crystals with short periodicity

    CERN Document Server

    Bazzan, Marco; Argiolas, Nicola; Busacca, Alessandro C; Oliveri, Roberto L; Stivala, Salvatore; Curcio, Luciano; Sanseverino, Stefano Riva; 10.1063/1.3264620

    2012-01-01

    Domain engineering technology in lithium tantalate is a well studied approach for nonlinear optical applications. However, for several cases of interest, the realization of short period structures (< 2 \\mu m) is required, which make their characterization difficult with standard techniques. In this work, we show that high resolution x-ray diffraction is a convenient approach for the characterization of such structures, allowing us to obtain in a nondestructive fashion information such as the average domain period, the domain wall inclination, and the overall structure quality.

  8. High-temperature electrical conductivity and electromechanical properties of stoichiometric lithium niobate

    OpenAIRE

    Ohlendorf, Gerd; Richter, Denny; Sauerwald, Jan; Fritze, Holger

    2016-01-01

    High temperature properties such as electrical conductivity (σ) and resonance behaviour of stoichiometric lithium niobate (LiNbO3) are determined in the temperature range from 20 to 950 °C. The activation energy of the conductivity is found to be 0.9 and 1.7 eV in the temperature range from 500 to 750 °C and from 800 to 950 °C, respectively. During thermal treatments in ambient air up to 950 °C and back, the conductivity remains unchanged at a given temperature, i.e., the crystal is st...

  9. Neutron noise measurements on Bugey 2 PWR

    Energy Technology Data Exchange (ETDEWEB)

    Marini, J.; Romy, D.; Spadi, J.C.; Assedo, R.; Castello, G.

    1982-01-01

    Following Bugey 2 PWR hot functional tests, dimension measurements of internals hold down spring led to suspect that vibration levels could change with time. Neutron noise measurements runs during the first cycle enabled describing vibration behaviour of internals. Comparisons with previous analytical and experimental results gained on the Safran model as well as on similar reactors were also made.

  10. Fabrication of ordered NiO coated Si nanowire array films as electrodes for a high performance lithium ion battery.

    Science.gov (United States)

    Qiu, M C; Yang, L W; Qi, X; Li, Jun; Zhong, J X

    2010-12-01

    Highly ordered NiO coated Si nanowire array films are fabricated as electrodes for a high performance lithium ion battery via depositing Ni on electroless-etched Si nanowires and subsequently annealing. The structures and morphologies of as-prepared films are characterized by X-ray diffraction, scanning electron microscopy, and transmission electron microscopy. When the potential window versus lithium was controlled, the coated NiO can be selected to be electrochemically active to store and release Li+ ions, while highly conductive crystalline Si cores function as nothing more than a stable mechanical support and an efficient electrical conducting pathway. The hybrid nanowire array films exhibit superior cyclic stability and reversible capacity compared to that of NiO nanostructured films. Owing to the ease of large-scale fabrication and superior electrochemical performance, these hybrid nanowire array films will be promising anode materials for high performance lithium-ion batteries.

  11. Carbon−Silicon Core−Shell Nanowires as High Capacity Electrode for Lithium Ion Batteries

    KAUST Repository

    Cui, Li-Feng

    2009-09-09

    We introduce a novel design of carbon-silicon core-shell nanowires for high power and long life lithium battery electrodes. Amorphous silicon was coated onto carbon nanofibers to form a core-shell structure and the resulted core-shell nanowires showed great performance as anode material. Since carbon has a much smaller capacity compared to silicon, the carbon core experiences less structural stress or damage during lithium cycling and can function as a mechanical support and an efficient electron conducting pathway. These nanowires have a high charge storage capacity of ∼2000 mAh/g and good cycling life. They also have a high Coulmbic efficiency of 90% for the first cycle and 98-99.6% for the following cycles. A full cell composed of LiCoO2 cathode and carbon-silicon core-shell nanowire anode is also demonstrated. Significantly, using these core-shell nanowires we have obtained high mass loading and an area capacity of ∼4 mAh/cm2, which is comparable to commercial battery values. © 2009 American Chemical Society.

  12. Trimethylsilylcyclopentadiene as a novel electrolyte additive for high temperature application of lithium nickel manganese oxide cathode

    Science.gov (United States)

    Tu, Wenqiang; Ye, Changchun; Yang, Xuerui; Xing, Lidan; Liao, Youhao; Liu, Xiang; Li, Weishan

    2017-10-01

    Electrolyte additives are necessary for the application of high potential cathode in high energy density lithium ion batteries, especially at elevated temperature. However, the electrolyte additives that can effectively suppress the dissolution of transition metal ions from cathode have seldom been developed up to date. In this work, we propose a novel electrolyte additive, trimethylsilylcyclopentadiene (SE), for high temperature application of a representative high potential cathode, lithium nickel manganese oxide (LiNi0.5Mn1.5O4). It is found that the dissolution of Mn and Ni from LiNi0.5Mn1.5O4 can be effectively suppressed by applying SE. With applying 0.25% SE, the dissolved amount of Mn and Ni is decreased by 97.4% and 98%, respectively, after 100 cycles at 55 °C. Correspondingly, the cyclic performance of LiNi0.5Mn1.5O4 is significantly improved. Physical characterizations and electrochemical measurements show that SE can be preferentially oxidized and generate a protective film on LiNi0.5Mn1.5O4. The resulting film inhibits the electrolyte decomposition and the transition metal ion dissolution.

  13. High flash point electrolyte for use in lithium-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Isken, P.; Dippel, C.; Schmitz, R.; Schmitz, R.W.; Kunze, M.; Passerini, S.; Winter, M. [Institute of Physical Chemistry, Westfaelische Wilhelms-University Muenster, Corrensstrasse 28/30, 48149 Muenster (Germany); Lex-Balducci, A., E-mail: a.lex-balducci@uni-muenster.de [Institute of Physical Chemistry, Westfaelische Wilhelms-University Muenster, Corrensstrasse 28/30, 48149 Muenster (Germany)

    2011-09-01

    Highlights: > Substitution of linear carbonates in conventional electrolytes with adiponitrile allows the realization of high flash point electrolytes. > EC:ADN based electrolytes display a higher anodic stability than a conventional electrolyte based on EC:DEC. > Graphite and NCM electrodes used in combination with the EC:ADN based electrolyte display a performance comparable with that of conventional electrolytes. - Abstract: The high flash point solvent adiponitrile (ADN) was investigated as co-solvent with ethylene carbonate (EC) for use as lithium-ion battery electrolyte. The flash point of this solvent mixture was more than 110 deg. C higher than that of conventional electrolyte solutions involving volatile linear carbonate components, such as diethyl carbonate (DEC) or dimethyl carbonate (DMC). The electrolyte based on EC:ADN (1:1 wt) with lithium tetrafluoroborate (LiBF{sub 4}) displayed a conductivity of 2.6 mS cm{sup -1} and no aluminum corrosion. In addition, it showed higher anodic stability on a Pt electrode than the standard electrolyte 1 M lithium hexafluorophosphate (LiPF{sub 6}) in EC:DEC (3:7 wt). Graphite/Li half cells using this electrolyte showed excellent rate capability up to 5C and good cycling stability (more than 98% capacity retention after 50 cycles at 1C). Additionally, the electrolyte was investigated in NCM/Li half cells. The cells were able to reach a capacity of 104 mAh g{sup -1} at 5C and capacity retention of more than 97% after 50 cycles. These results show that an electrolyte with a considerably increased flash point with respect to common electrolyte systems comprising linear carbonates, could be realized without any negative effects on the electrochemical performance in Li-half cells.

  14. Compact and high-particle-flux thermal-lithium-beam probe system for measurement of two-dimensional electron density profile.

    Science.gov (United States)

    Shibata, Y; Manabe, T; Kajita, S; Ohno, N; Takagi, M; Tsuchiya, H; Morisaki, T

    2014-09-01

    A compact and high-particle-flux thermal-lithium-beam source for two-dimensional measurement of electron density profiles has been developed. The thermal-lithium-beam oven is heated by a carbon heater. In this system, the maximum particle flux of the thermal lithium beam was ~4 × 10(19) m(-2) s(-1) when the temperature of the thermal-lithium-beam oven was 900 K. The electron density profile was evaluated in the small tokamak device HYBTOK-II. The electron density profile was reconstructed using the thermal-lithium-beam probe data and this profile was consistent with the electron density profile measured with a Langmuir electrostatic probe. We confirm that the developed thermal-lithium-beam probe can be used to measure the two-dimensional electron density profile with high time and spatial resolutions.

  15. Interaction of cyclic ageing at high-rate and low temperatures and safety in lithium-ion batteries

    Science.gov (United States)

    Fleischhammer, Meike; Waldmann, Thomas; Bisle, Gunther; Hogg, Björn-Ingo; Wohlfahrt-Mehrens, Margret

    2015-01-01

    The differences in the safety behaviour between un-aged and aged high-power 18650 lithium-ion cells were investigated at the cell and material level by Accelerating Rate Calorimetry (ARC) and Simultaneous Thermal Analysis (STA). Commercial cells containing a LixNi1/3Mn1/3Co1/3O2/LiyMn2O4 blend cathode, a carbon/graphite anode and a PP/PE/PP trilayer separator were aged by high-rate and low temperature cycling, leading to (i) mechanical deformation of the jelly roll and (ii) lithium plating on the anode. The results show a strong influence of the ageing history on the safety behaviour. While cycling at high current does not have a strong influence on the cell safety, lithium plating leads to a significant increase of heat formation during thermal runaway and thus to a higher hazard of safety.

  16. Iron titanium phosphates as high-specific-capacity electrode materials for lithium ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Essehli, R., E-mail: essehli.rachid@yahoo.fr [Laboratory of Mineral Solid and Analytical Chemistry (LMSAC), Department of Chemistry, Faculty of Sciences, University Mohamed I, PO. Box 717, 60000 Oujda (Morocco); ESECO SYSTEMS 270 rue Thomas Edison, Atelier Relais No 6, 34400 Lunel (France); El Bali, B. [Laboratory of Mineral Solid and Analytical Chemistry (LMSAC), Department of Chemistry, Faculty of Sciences, University Mohamed I, PO. Box 717, 60000 Oujda (Morocco); Faik, A. [CIC energigune, Parque Tecnológico de Álava, Albert Einstein 48, 01510 Miñano, Álava (Spain); Naji, M. [CNRS, UPR3079 CEMHTI, 1D avenue de la Recherche Scientifique, 45071 Orléans cedex 2 (France); Benmokhtar, S. [LCPGM, Laboratoire de Chimie-Physique Générale des Matériaux, Département de Chimie, Université Hassan II-Mohammedia, Faculté des Sciences Ben M’Sik, Casablanca (Morocco); Zhong, Y.R.; Su, L.W.; Zhou, Z. [Institute of New Energy Material Chemistry, Synergetic Innovation Center of Chemical Science and Engineering (Tianjin), Nankai University, Tianjin 300071 (China); Kim, J.; Kang, K. [Department of Materials Science and Engineering, Seoul National University, Gwanak-ro, Gwanak-gu, Seoul 151-742 (Korea, Republic of); Dusek, M. [Institute of Physics of the ASCR, v.v.i., Na Slovance 2, 182 21 Praha 8 (Czech Republic)

    2014-02-05

    Highlights: • Iron Titanium Phosphates as High-Specific-Capacity. • Electrode Materials for Lithium ion Batteries. • During the following cycles, good reversible capacity retention and better cyclabilit. • Ex-situ XRD analysis during the first discharge shows an amorphization of this anode material. -- Abstract: Two iron titanium phosphates, Fe{sub 0.5}TiOPO{sub 4} and Fe{sub 0.5}Ti{sub 2}(PO{sub 4}){sub 3}, were prepared, and their crystal structures and electrochemical performances were compared. The electrochemical measurements of Fe{sub 0.5}TiOPO{sub 4} as an anode of a lithium ion cell showed that upon the first discharge down to 0.5 V, the cell delivered a capacity of 560 mA h/g, corresponding to the insertion of 5 Li’s per formula unit Fe{sub 0.5}TiOPO{sub 4}. Ex-situ XRD reveals a gradual evolution of the structure during cycling of the material, with lower crystallinity after the first discharge cycle. By correlating the electrochemical performances with the structural studies, new insights are achieved into the electrochemical behaviour of the Fe{sub 0.5}TiOPO{sub 4} anode material, suggesting a combination of intercalation and conversion reactions. The Nasicon-type Fe{sub 0.5}Ti{sub 2}(PO{sub 4}){sub 3} consists of a three-dimensional network made of corners and edges sharing [TiO{sub 6}] and [FeO{sub 6}] octahedra and [PO{sub 4}] tetrahedra leading to the formation of trimmers [FeTi{sub 2}O{sub 12}]. The first discharge of lithium ion cells based on Fe{sub 0.5}Ti{sub 2}(PO{sub 4}){sub 3} materials showed electrochemical activity of Ti{sup 4+}/Ti{sup 3+} and Fe{sup 2+}/Fe{sup 0} couples in the 2.5–1 V region. Below this voltage, the discharge profiles are typical of phosphate systems where Li{sub 3}PO{sub 4} is a product of the electrochemical reaction with lithium; moreover, the electrolyte solvent is reduced. An initial capacities as high as 1100 mA h g{sup −1} can be obtained at deep discharge. However, there is an irreversible capacity

  17. Sustainable, heat-resistant and flame-retardant cellulose-based composite separator for high-performance lithium ion battery

    Science.gov (United States)

    Zhang, Jianjun; Yue, Liping; Kong, Qingshan; Liu, Zhihong; Zhou, Xinhong; Zhang, Chuanjian; Xu, Quan; Zhang, Bo; Ding, Guoliang; Qin, Bingsheng; Duan, Yulong; Wang, Qingfu; Yao, Jianhua; Cui, Guanglei; Chen, Liquan

    2014-02-01

    A sustainable, heat-resistant and flame-retardant cellulose-based composite nonwoven has been successfully fabricated and explored its potential application for promising separator of high-performance lithium ion battery. It was demonstrated that this flame-retardant cellulose-based composite separator possessed good flame retardancy, superior heat tolerance and proper mechanical strength. As compared to the commercialized polypropylene (PP) separator, such composite separator presented improved electrolyte uptake, better interface stability and enhanced ionic conductivity. In addition, the lithium cobalt oxide (LiCoO2)/graphite cell using this composite separator exhibited better rate capability and cycling retention than that for PP separator owing to its facile ion transport and excellent interfacial compatibility. Furthermore, the lithium iron phosphate (LiFePO4)/lithium cell with such composite separator delivered stable cycling performance and thermal dimensional stability even at an elevated temperature of 120°C. All these fascinating characteristics would boost the application of this composite separator for high-performance lithium ion battery.

  18. Suppressed gross erosion of high-temperature lithium via rapid deuterium implantation

    Science.gov (United States)

    Abrams, T.; Jaworski, M. A.; Chen, M.; Carter, E. A.; Kaita, R.; Stotler, D. P.; De Temmerman, G.; Morgan, T. W.; van den Berg, M. A.; van der Meiden, H. J.

    2016-01-01

    Lithium-coated high-Z substrates are planned for use in the NSTX-U divertor and are a candidate plasma facing component (PFC) for reactors, but it remains necessary to characterize the gross Li erosion rate under high plasma fluxes (>1023 m-2 s-1), typical for the divertor region. In this work, a realistic model for the compositional evolution of a Li/D layer is developed that incorporates first principles molecular dynamics (MD) simulations of D diffusion in liquid Li. Predictions of Li erosion from a mixed Li/D material are also developed that include formation of lithium deuteride (LiD). The erosion rate of Li from LiD is predicted to be significantly lower than from pure Li. This prediction is tested in the Magnum-PSI linear plasma device at ion fluxes of 1023-1024 m-2 s-1 and Li surface temperatures  ⩽800 °C. Li/LiD coatings ranging in thickness from 0.2 to 500 μm are studied. The dynamic D/Li concentrations are inferred via diffusion simulations. The pure Li erosion rate remains greater than Langmuir Law evaporation, as expected. For mixed-material Li/LiD surfaces, the erosion rates are reduced, in good agreement with modelling in almost all cases. These results imply that the temperature limit for a Li-coated PFC may be significantly higher than previously imagined.

  19. CuO nanorods/graphene nanocomposites for high-performance lithium-ion battery anodes

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Qi; Zhao, Jun; Shan, Wanfei; Xia, Xinbei; Xing, Lili; Xue, Xinyu, E-mail: xuexinyu@mail.neu.edu.cn

    2014-03-25

    Highlights: • CuO/GNS nanocomposites are synthesized by a hydrothermal method. • CuO/GNSs as LIB anodes exhibit much higher cyclability and capacity than CuO nanostructures. • Such excellent performances can be attributed to the synergistic effect between CuO and GNSs. -- Abstract: CuO/graphene nanocomposites are synthesized by a hydrothermal method, and their application as anodes of lithium-ion batteries has been investigated. CuO nanorods are uniformly coating on the surface of graphene nanosheets. CuO/graphene nanocomposites exhibit high cyclability and capacity. After 50 cycles, the capacity can maintain at 692.5 mA h g{sup −1} at 0.1 C rate (10 h per half cycle). Such a high performance can be attributed to the synergistic effect between graphene nanosheets and CuO nanorods. The present results indicate that CuO/graphene nanocomposites have potential applications in the anodes of lithium-ion battery.

  20. Synthesis of High-Quality α-MnSe Nanostructures with Superior Lithium Storage Properties.

    Science.gov (United States)

    Li, Na; Zhang, Yi; Zhao, Hongyang; Liu, Zhengqing; Zhang, Xinyu; Du, Yaping

    2016-03-21

    High-quality α-MnSe nanocubes were successfully prepared for the first time by an effective hot injection synthesis strategy. This approach was simple but robust and had been applied to the controllable synthesis of different sizes and diverse morphologies of α-MnSe nanostructures. The crystal phases, compositions, and microstructures of these nanostructures had been systematically characterized with a series of techniques. As a proof-of-concept application, the as-prepared α-MnSe nanocubes were used as an anode material for a lithium ion battery, which exhibited superior rate ability and ultralong cycle stability in half-cell and full-cell tests. Importantly, the phase transition from α-MnSe to β-MnSe during the electrochemical process was proved by ex situ X-ray diffraction and selected area electron diffraction. The excellent electrochemical performance of α-MnSe endowed its potential as an anode material candidate for high performance lithium storage.

  1. Hierarchical columnar silicon anode structures for high energy density lithium sulfur batteries

    Science.gov (United States)

    Piwko, Markus; Kuntze, Thomas; Winkler, Sebastian; Straach, Steffen; Härtel, Paul; Althues, Holger; Kaskel, Stefan

    2017-05-01

    Silicon is a promising anode material for next generation lithium secondary batteries. To significantly increase the energy density of state of the art batteries with silicon, new concepts have to be developed and electrode structuring will become a key technology. Structuring is essential to reduce the macroscopic and microscopic electrode deformation, caused by the volume change during cycling. We report pulsed laser structuring for the generation of hierarchical columnar silicon films with outstanding high areal capacities up to 7.5 mAh cm-2 and good capacity retention. Unstructured columnar electrodes form a micron-sized block structure during the first cycle to compensate the volume expansion leading to macroscopic electrode deformation. At increased silicon loading, without additional structuring, pronounced distortion and the formation of cracks through the current collector causes cell failure. Pulsed laser ablation instead is demonstrated to avoid macroscopic electrode deformation by initial formation of the block structure. A full cell with lithiated silicon versus a carbon-sulfur cathode is assembled with only 15% overbalanced anode and low electrolyte amount (8 μl mgsulfur-1). While the capacity retention over 50 cycles is identical to a cell with high excess lithium anode, the volumetric energy density could be increased by 30%.

  2. Electrolytes for Use in High Energy Lithium-ion Batteries with Wide Operating Temperature Range

    Science.gov (United States)

    Smart, Marshall C.; Ratnakumar, B. V.; West, W. C.; Whitcanack, L. D.; Huang, C.; Soler, J.; Krause, F. C.

    2012-01-01

    Met programmatic milestones for program. Demonstrated improved performance with wide operating temperature electrolytes containing ester co-solvents (i.e., methyl butyrate) containing electrolyte additives in A123 prototype cells: Previously demonstrated excellent low temperature performance, including 11C rates at -30 C and the ability to perform well down to -60 C. Excellent cycle life at room temperature has been displayed, with over 5,000 cycles being demonstrated. Good high temperature cycle life performance has also been achieved. Demonstrated improved performance with methyl propionate-containing electrolytes in large capacity prototype cells: Demonstrated the wide operating temperature range capability in large cells (12 Ah), successfully scaling up technology from 0.25 Ah size cells. Demonstrated improved performance at low temperature and good cycle life at 40 C with methyl propionate-based electrolyte containing increasing FEC content and the use of LiBOB as an additive. Utilized three-electrode cells to investigate the electrochemical characteristics of high voltage systems coupled with wide operating temperature range electrolytes: From Tafel polarization measurements on each electrode, it is evident the NMC-based cathode displays poor lithium kinetics (being the limiting electrode). The MB-based formulations containing LiBOB delivered the best rate capability at low temperature, which is attributed to improved cathode kinetics. Whereas, the use of lithium oxalate as an additive lead to the highest reversible capacity and lower irreversible losses.

  3. A trilayer separator with dual function for high performance lithium-sulfur batteries

    Science.gov (United States)

    Song, Rensheng; Fang, Ruopian; Wen, Lei; Shi, Ying; Wang, Shaogang; Li, Feng

    2016-01-01

    In this article, we propose a trilayer graphene/polypropylene/Al2O3 (GPA) separator with dual function for high performance lithium-sulfur (Li-S) batteries. Graphene is coated on one side of polypropylene (PP) separator, which functions as a conductive layer and an electrolyte reservoir that allows for rapid electron and ion transport. Then Al2O3 particles are coated on the other side to further enhance thermal stability and safety of the graphene coated polypropylene (GCP) separator, which are touched with lithium metal anode in the Li-S battery. The GPA separator shows good thermal stability after heating at 157 °C for 10 min while both GCP and PP separators showing an obvious shrinkage about 10%. The initial discharge specific capacity of Li-S coin cell with a GPA separator could reach 1067.7 mAh g-1 at 0.2C. After 100 discharge/charge cycles, it can still deliver a reversible capacity of as high as 804.4 mAh g-1 with 75% capacity retention. The pouch cells further confirm that the trilayer design has great promise towards practical applications.

  4. Preparation of lithium ferrite nanoparticles by high energy ball milling and characterizations

    Directory of Open Access Journals (Sweden)

    J. Touthang

    2016-11-01

    Full Text Available Ferrites are ferrimagnetic ceramic materials with inherent useful electromagnetic properties. Of them, spinelstructured ferrites are promising materials for microwave device applications; stress/torsion sensors and energy storage applications like anode materials in lithium batteries, fuel cells, solar cells etc. Nanostructured spinels further have high and wide scope of potential applications. In the present study, two different types of varied sized ferrimagnetic lithium ferrite spinel nanoparticles prepared using chemical sol-gel auto-combustion method were chosen. The prepared spinel particles were heated at 300°C for 1h. After heating the powders were milled using a High Energy Ball Mill for 30 minutes to further grind the particles and then subjected to various characterizations. Structural characterization was done using X-Ray Diffraction Method (XRD. The study revealed the spinel structure of these samples. Structural parameter such as lattice constant was determined using XRD data and found that the lattice parameter agrees with the standard data. DLS study found the agglomerations of the nanoparticles. The synthesized nanospinel particles were also characterized by the UVVis Spectroscopy, the Fourier Transform Infrared Spectroscopy (FTIR. Finally the magnetic hysteresis properties were studied using a Vibrating Sample Magnetometer (VSM.

  5. Review on anionic redox for high-capacity lithium- and sodium-ion batteries

    Science.gov (United States)

    Zhao, Chenglong; Wang, Qidi; Lu, Yaxiang; Hu, Yong-Sheng; Li, Baohua; Chen, Liquan

    2017-05-01

    Rechargeable batteries, especially lithium-ion batteries, are now widely used as power sources for portable electronics and electric vehicles, but material innovations are still needed to satisfy the increasing demand for larger energy density. Recently, lithium- and sodium-rich electrode materials, including the A2MO3-family layered compounds (A  =  Li, Na; M  =  Mn4+, Ru4+, etc), have been extensively studied as potential high-capacity electrode materials for a cumulative cationic and anionic redox activity. Negatively charged oxide ions can potentially donate electrons to compensate for the absence of oxidable transition metals as a redox center to further increase the reversible capacity. Understanding and controlling the state-of-the-art anionic redox processes is pivotal for the design of advanced energy materials, highlighted in rechargeable batteries. Hence, experimental and theoretical approaches have been developed to consecutively study the diverting processes, states, and structures involved. In this review, we attempt to present a literature overview and provide insight into the reaction mechanism with respect to the anionic redox processes, proposing some opinions as target oriented. It is hoped that, through this discussion, the search for anionic redox electrode materials with high-capacity rechargeable batteries can be advanced, and practical applications realized as soon as possible.

  6. Electrolytes for Use in High Energy Lithium-ion Batteries with Wide Operating Temperature Range

    Science.gov (United States)

    Smart, Marshall C.; Ratnakumar, B. V.; West, W. C.; Whitcanack, L. D.; Huang, C.; Soler, J.; Krause, F. C.

    2012-01-01

    Met programmatic milestones for program. Demonstrated improved performance with wide operating temperature electrolytes containing ester co-solvents (i.e., methyl butyrate) containing electrolyte additives in A123 prototype cells: Previously demonstrated excellent low temperature performance, including 11C rates at -30 C and the ability to perform well down to -60 C. Excellent cycle life at room temperature has been displayed, with over 5,000 cycles being demonstrated. Good high temperature cycle life performance has also been achieved. Demonstrated improved performance with methyl propionate-containing electrolytes in large capacity prototype cells: Demonstrated the wide operating temperature range capability in large cells (12 Ah), successfully scaling up technology from 0.25 Ah size cells. Demonstrated improved performance at low temperature and good cycle life at 40 C with methyl propionate-based electrolyte containing increasing FEC content and the use of LiBOB as an additive. Utilized three-electrode cells to investigate the electrochemical characteristics of high voltage systems coupled with wide operating temperature range electrolytes: From Tafel polarization measurements on each electrode, it is evident the NMC-based cathode displays poor lithium kinetics (being the limiting electrode). The MB-based formulations containing LiBOB delivered the best rate capability at low temperature, which is attributed to improved cathode kinetics. Whereas, the use of lithium oxalate as an additive lead to the highest reversible capacity and lower irreversible losses.

  7. Sb nanoparticles encapsulated into porous carbon matrixes for high-performance lithium-ion battery anodes

    Science.gov (United States)

    Yi, Zheng; Han, Qigang; Zan, Ping; Wu, Yaoming; Cheng, Yong; Wang, Limin

    2016-11-01

    A novel Sb/C polyhedra composite is successfully fabricated by a galvanic replacement reaction technique using metal organic frameworks as templates. In this composite, the ultrasmall Sb nanoparticles with an average size of 15 nm are homogeneously encapsulated into the carbon matrixes, forming a hierarchical porous structure with nanosized building blocks. Used as an anode material for lithium ion batteries, this composite exhibits high lithium storage capacities, excellent rate capability and superior cycle stability, higher than many reported results. Notably, a discharge capacity of 565 mAh g-1 at a current density of 0.2 A g-1 is delivered after 100 repeated cycles. Even at a high current density of 1 A g-1, a discharge capacity of 400.5 mAh g-1 is also maintained after 500 cycles. Such superior cycling stability and rate discharge performance of the designed Sb/C composite can be attributed to the synergistic effect between Sb nanoparticles and the porous carbon matrixes.

  8. Conductivity, dielectric behavior and FTIR studies of high molecular weight poly(vinylchloride)-lithium triflate polymer electrolytes

    Energy Technology Data Exchange (ETDEWEB)

    Ramesh, S. [Faculty of Engineering and Science, Universiti Tunku Abdul Rahman, Setapak, 53300 Kuala Lumpur (Malaysia)]. E-mail: ramesh@mail.utar.edu.my; Chai, M.F. [Faculty of Engineering and Science, Universiti Tunku Abdul Rahman, Setapak, 53300 Kuala Lumpur (Malaysia)

    2007-05-15

    Thin films of high molecular weight polyvinyl chloride (PVC) with lithium triflate (LiCF{sub 3}SO{sub 3}) salt were prepared by solution casting method. The ionic conductivity and dielectric measurements were carried out on these films over a wide frequency regime at various temperatures. The conductivity-temperature plots were found to obey classical Arrhenius relationship. The dielectric behavior was analysed using dielectric permittivity and dielectric modulus of the samples. FTIR studies show some simple overlapping and shift in peaks between high molecular weight polyvinyl chloride (PVC) with lithium triflate (LiCF{sub 3}SO{sub 3}) salt in the polymer electrolyte complexes.

  9. Thermoelectric properties of high pressure synthesized lithium and calcium double-filled CoSb3

    Directory of Open Access Journals (Sweden)

    Xiaohui Li

    2017-01-01

    Full Text Available Lithium and calcium are inefficient filling elements of CoSb3 at ambient pressure, but show nice filling behavior under high pressure. In this work, we synthesized Li/Ca double-filled CoSb3 with high pressure synthesis method. The products show the skutterudite structure of Im3¯ symmetry. Thermoelectric properties were effectively enhanced through Li and Ca co-filling. For the optimal Li0.08Ca0.18Co4Sb12 sample, the power factor maintains a relatively high value over the whole measurement temperature range and peaks at 4700μWm−1K−2, meanwhile the lattice thermal conductivity is greatly suppressed, leading to a maximal ZT of 1.18 at 700 K. Current work demonstrates high pressure synthesis as an effective method to produce multiple elemental filled CoSb3 skutterudites.

  10. Ceramic separators based on Li+-conducting inorganic electrolyte for high-performance lithium-ion batteries with enhanced safety

    Science.gov (United States)

    Jung, Yun-Chae; Kim, Seul-Ki; Kim, Moon-Sung; Lee, Jeong-Hye; Han, Man-Seok; Kim, Duck-Hyun; Shin, Woo-Cheol; Ue, Makoto; Kim, Dong-Won

    2015-10-01

    Flexible ceramic separators based on Li+-conducting lithium lanthanum zirconium oxide are prepared as thin films and directly applied onto negative electrode to produce a separator-electrode assembly with good interfacial adhesion and low interfacial resistances. The ceramic separators show an excellent thermal stability and high ionic conductivity as compared to conventional polypropylene separator. The lithium-ion batteries assembled with graphite negative electrode, Li+-conducting ceramic separator and LiCoO2 positive electrode exhibit good cycling performance in terms of discharge capacity, capacity retention and rate capability. It is also demonstrated that the use of a ceramic separator can greatly improve safety over cells employing a polypropylene separator, which is highly desirable for lithium-ion batteries with enhanced safety.

  11. TiC/NiO Core/Shell Nanoarchitecture with Battery-Capacitive Synchronous Lithium Storage for High-Performance Lithium-Ion Battery.

    Science.gov (United States)

    Huang, Hui; Feng, Tong; Gan, Yongping; Fang, Mingyu; Xia, Yang; Liang, Chu; Tao, Xinyong; Zhang, Wenkui

    2015-06-10

    The further development of electrode materials with high capacity and excellent rate capability presents a great challenge for advanced lithium-ion batteries. Herein, we demonstrate a battery-capacitive synchronous lithium storage mechanism based on a scrupulous design of TiC/NiO core/shell nanoarchitecture, in which the TiC nanowire core exhibits a typical double-layer capacitive behavior, and the NiO nanosheet shell acts as active materials for Li(+) storage. The as-constructed TiC/NiO (32 wt % NiO) core/shell nanoarchitecture offers high overall capacity and excellent cycling ability, retaining above 507.5 mAh g(-1) throughout 60 cycles at a current density of 200 mA g(-1) (much higher than theoretical value of the TiC/NiO composite). Most importantly, the high rate capability is far superior to that of NiO or other metal oxide electrode materials, owing to its double-layer capacitive characteristics of TiC nanowire and intrinsic high electrical conductivity for facile electron transport during Li(+) storage process. Our work offers a promising approach via a rational hybridization of two electrochemical energy storage materials for harvesting high capacity and good rate performance.

  12. The origin of high electrolyte-electrode interfacial resistances in lithium cells containing garnet type solid electrolytes.

    Science.gov (United States)

    Cheng, Lei; Crumlin, Ethan J; Chen, Wei; Qiao, Ruimin; Hou, Huaming; Franz Lux, Simon; Zorba, Vassilia; Russo, Richard; Kostecki, Robert; Liu, Zhi; Persson, Kristin; Yang, Wanli; Cabana, Jordi; Richardson, Thomas; Chen, Guoying; Doeff, Marca

    2014-09-14

    Dense LLZO (Al-substituted Li7La3Zr2O12) pellets were processed in controlled atmospheres to investigate the relationships between the surface chemistry and interfacial behavior in lithium cells. Laser induced breakdown spectroscopy (LIBS), scanning electron microscopy (SEM), X-ray diffraction (XRD), Raman spectroscopy, synchrotron X-ray photoelectron spectroscopy (XPS) and soft X-ray absorption spectroscopy (XAS) studies revealed that Li2CO3 was formed on the surface when LLZO pellets were exposed to air. The distribution and thickness of the Li2CO3 layer were estimated by a combination of bulk and surface sensitive techniques with various probing depths. First-principles thermodynamic calculations confirmed that LLZO has an energetic preference to form Li2CO3 in air. Exposure to air and the subsequent formation of Li2CO3 at the LLZO surface is the source of the high interfacial impedances observed in cells with lithium electrodes. Surface polishing can effectively remove Li2CO3 and dramatically improve the interfacial properties. Polished samples in lithium cells had an area specific resistance (ASR) of only 109 Ω cm(2) for the LLZO/Li interface, the lowest reported value for Al-substituted LLZO. Galvanostatic cycling results obtained from lithium symmetrical cells also suggest that the quality of the LLZO/lithium interface has a significant impact on the device lifetime.

  13. High Temperature Stable Separator for Lithium Batteries Based on SiO₂ and Hydroxypropyl Guar Gum.

    Science.gov (United States)

    Carvalho, Diogo Vieira; Loeffler, Nicholas; Kim, Guk-Tae; Passerini, Stefano

    2015-10-23

    A novel membrane based on silicon dioxide (SiO₂) and hydroxypropyl guar gum (HPG) as binder is presented and tested as a separator for lithium-ion batteries. The separator is made with renewable and low cost materials and an environmentally friendly manufacturing processing using only water as solvent. The separator offers superior wettability and high electrolyte uptake due to the optimized porosity and the good affinity of SiO₂ and guar gum microstructure towards organic liquid electrolytes. Additionally, the separator shows high thermal stability and no dimensional-shrinkage at high temperatures due to the use of the ceramic filler and the thermally stable natural polymer. The electrochemical tests show the good electrochemical stability of the separator in a wide range of potential, as well as its outstanding cycle performance.

  14. High elastic modulus polymer electrolytes suitable for preventing thermal runaway in lithium batteries

    Science.gov (United States)

    Mullin, Scott; Panday, Ashoutosh; Balsara, Nitash Pervez; Singh, Mohit; Eitouni, Hany Basam; Gomez, Enrique Daniel

    2014-04-22

    A polymer that combines high ionic conductivity with the structural properties required for Li electrode stability is useful as a solid phase electrolyte for high energy density, high cycle life batteries that do not suffer from failures due to side reactions and dendrite growth on the Li electrodes, and other potential applications. The polymer electrolyte includes a linear block copolymer having a conductive linear polymer block with a molecular weight of at least 5000 Daltons, a structural linear polymer block with an elastic modulus in excess of 1.times.10.sup.7 Pa and an ionic conductivity of at least 1.times.10.sup.-5 Scm.sup.-1. The electrolyte is made under dry conditions to achieve the noted characteristics. In another aspect, the electrolyte exhibits a conductivity drop when the temperature of electrolyte increases over a threshold temperature, thereby providing a shutoff mechanism for preventing thermal runaway in lithium battery cells.

  15. Hierarchical mesoporous/microporous carbon with graphitized frameworks for high-performance lithium-ion batteries

    Directory of Open Access Journals (Sweden)

    Yingying Lv

    2014-11-01

    Full Text Available A hierarchical meso-/micro-porous graphitized carbon with uniform mesopores and ordered micropores, graphitized frameworks, and extra-high surface area of ∼2200 m2/g, was successfully synthesized through a simple one-step chemical vapor deposition process. The commercial mesoporous zeolite Y was utilized as a meso-/ micro-porous template, and the small-molecule methane was employed as a carbon precursor. The as-prepared hierarchical meso-/micro-porous carbons have homogeneously distributed mesopores as a host for electrolyte, which facilitate Li+ ions transport to the large-area micropores, resulting a high reversible lithium ion storage of 1000 mA h/g and a high columbic efficiency of 65% at the first cycle.

  16. VERA Core Simulator Methodology for PWR Cycle Depletion

    Energy Technology Data Exchange (ETDEWEB)

    Kochunas, Brendan [University of Michigan; Collins, Benjamin S [ORNL; Jabaay, Daniel [University of Michigan; Kim, Kang Seog [ORNL; Graham, Aaron [University of Michigan; Stimpson, Shane [University of Michigan; Wieselquist, William A [ORNL; Clarno, Kevin T [ORNL; Palmtag, Scott [Core Physics, Inc.; Downar, Thomas [University of Michigan; Gehin, Jess C [ORNL

    2015-01-01

    This paper describes the methodology developed and implemented in MPACT for performing high-fidelity pressurized water reactor (PWR) multi-cycle core physics calculations. MPACT is being developed primarily for application within the Consortium for the Advanced Simulation of Light Water Reactors (CASL) as one of the main components of the VERA Core Simulator, the others being COBRA-TF and ORIGEN. The methods summarized in this paper include a methodology for performing resonance self-shielding and computing macroscopic cross sections, 2-D/1-D transport, nuclide depletion, thermal-hydraulic feedback, and other supporting methods. These methods represent a minimal set needed to simulate high-fidelity models of a realistic nuclear reactor. Results demonstrating this are presented from the simulation of a realistic model of the first cycle of Watts Bar Unit 1. The simulation, which approximates the cycle operation, is observed to be within 50 ppm boron (ppmB) reactivity for all simulated points in the cycle and approximately 15 ppmB for a consistent statepoint. The verification and validation of the PWR cycle depletion capability in MPACT is the focus of two companion papers.

  17. Developments of high-voltage all-solid-state thin-film lithium ion batteries

    Science.gov (United States)

    Schwenzel, J.; Thangadurai, V.; Weppner, W.

    Powders of Li 2MMn 3O 8 (M = Fe, Co) were prepared by glycine nitrate combustion from the corresponding metal nitrates. The reaction products were pressed into pellets with the addition of 20 wt.% excess LiNO 3, which were used as targets for e-beam evaporation. A high-voltage all-solid-state thin-film lithium ion battery was demonstrated by the sequential deposition of spinel structured Li 2MMn 3O 8 (M = Co, Fe) as positive electrode by e-beam evaporation, LiPON as electrolyte, and metallic Al as negative electrode by sputtering in N 2 and Ar gas mixtures with specific power and gas flow rates. A lithium ion conductivity of ∼10 -6 S cm -1 was observed for the optimized thin-film LiPON electrolyte prepared under the condition of a chamber pressure of 2.6 × 10 -2 mbar and a power of 60-100 W. The chemical diffusion coefficient (D ˜) was found to be in the range 10 -13 to 10 -12 cm 2 s -1 for any composition x of Li 2- xMMn 3O 8 (M = Fe, Co) in the range from 0.1 to 1.6 by employing the galvanostatic intermittent titration technique (GITT). AC impedance studies revealed a charge transfer resistance of 260-290 Ω, a double layer capacity of ∼45-70 μF for an electrode area of 6.7 cm 2.

  18. Performance degradation of high-power lithium-ion cells-Electrochemistry of harvested electrodes

    Science.gov (United States)

    Abraham, D. P.; Knuth, J. L.; Dees, D. W.; Bloom, I.; Christophersen, J. P.

    The performance of 18650-type high-power lithium-ion cells is being evaluated as part of the U.S. Department of Energy's (DOEs) Advanced Technology Development (ATD) program. In this article, we present accelerated aging data acquired on 18650-cells containing LiNi 0.8Co 0.15Al 0.05O 2- or LiNi 0.8Co 0.1Al 0.1O 2-based positive electrodes, MAG-10 graphite-based negative electrodes, and 1.2-M LiPF 6 in EC:EMC (3:7 by wt.) electrolyte. Capacity and impedance data acquired on electrodes harvested from these cells highlight the contributions of the positive and negative electrodes to the degradation of cell performance. We also describe test methodologies used to examine the electrochemical characteristics of the harvested electrodes. Identifying and optimizing cell components responsible for performance degradation should enable the development of new lithium-ion cell chemistries that will meet the 15-year cell calendar life goal established by DOEs FreedomCar initiative.

  19. Diagnostic examination of thermally abused high-power lithium-ion cells

    Science.gov (United States)

    Abraham, D. P.; Roth, E. P.; Kostecki, R.; McCarthy, K.; MacLaren, S.; Doughty, D. H.

    The inherent thermal instability of lithium-ion cells is a significant impediment to their widespread commercialization for hybrid-electric vehicle applications. Cells containing conventional organic electrolyte-based chemistries are prone to thermal runaway at temperatures around 180 °C. We conducted accelerating rate calorimetry measurements on high-power 18650-type lithium-ion cells in an effort to decipher the sequence of events leading to thermal runaway. In addition, electrode and separator samples harvested from a cell that was heated to 150 °C then air-quenched to room temperature were examined by microscopy, spectroscopy, and diffraction techniques. Self-heating of the cell began at 84 °C. The gases generated in the cell included CO 2 and CO, and smaller quantities of H 2, C 2H 4, CH 4, and C 2H 6. The main changes on cell heating to 150 °C were observed on the anode surface, which was covered by a thick layer of surface deposits that included LiF and inorganic and organo-phosphate compounds. The sources of gas generation and the mechanisms leading to the formation of compounds observed on the electrode surfaces are discussed.

  20. Performance degradation of high-power lithium-ion cells - Electrochemistry of harvested electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Abraham, D.P.; Knuth, J.L.; Dees, D.W.; Bloom, I. [Argonne National Laboratory, Argonne, IL 60439 (United States); Christophersen, J.P. [Idaho National Laboratory, Idaho Falls, ID 83415 (United States)

    2007-07-10

    The performance of 18650-type high-power lithium-ion cells is being evaluated as part of the U.S. Department of Energy's (DOEs) Advanced Technology Development (ATD) program. In this article, we present accelerated aging data acquired on 18650-cells containing LiNi{sub 0.8}Co{sub 0.15}Al{sub 0.05}O{sub 2}- or LiNi{sub 0.8}Co{sub 0.1}Al{sub 0.1}O{sub 2}-based positive electrodes, MAG-10 graphite-based negative electrodes, and 1.2-M LiPF{sub 6} in EC:EMC (3:7 by wt.) electrolyte. Capacity and impedance data acquired on electrodes harvested from these cells highlight the contributions of the positive and negative electrodes to the degradation of cell performance. We also describe test methodologies used to examine the electrochemical characteristics of the harvested electrodes. Identifying and optimizing cell components responsible for performance degradation should enable the development of new lithium-ion cell chemistries that will meet the 15-year cell calendar life goal established by DOEs FreedomCar initiative. (author)

  1. A paramagnetic implant containing lithium naphthalocyanine microcrystals for high-resolution biological oximetry.

    Science.gov (United States)

    Meenakshisundaram, Guruguhan; Pandian, Ramasamy P; Eteshola, Edward; Lee, Stephen C; Kuppusamy, Periannan

    2010-03-01

    Lithium naphthalocyanine (LiNc) is a microcrystalline EPR oximetry probe with high sensitivity to oxygen [R.P. Pandian, M. Dolgos, C. Marginean, P.M. Woodward, P.C. Hammel, P.T. Manoharan, P. Kuppusamy, Molecular packing and magnetic properties of lithium naphthalocyanine crystal: hollow channels enabling permeability and paramagnetic sensitivity to molecular oxygen J. Mater. Chem. 19 (2009) 4138-4147]. However, direct implantation of the crystals in the tissue for in vivo oxygen measurements may be hindered by concerns associated with their direct contact with the tissue/cells and loss of EPR signal due to particle migration in the tissue. In order to address these concerns, we have developed encapsulations (chips) of LiNc microcrystals in polydimethyl siloxane (PDMS), an oxygen-permeable, bioinert polymer. Oximetry evaluation of the fabricated chips revealed that the oxygen sensitivity of the crystals was unaffected by encapsulation in PDMS. Chips were stable against sterilization procedures or treatment with common biological oxidoreductants. In vivo oxygen measurements established the ability of the chips to provide reliable and repeated measurements of tissue oxygenation. This study establishes PDMS-encapsulated LiNc as a potential probe for long-term and repeated measurements of tissue oxygenation. Copyright (c) 2009 Elsevier Inc. All rights reserved.

  2. Mass spectrometric studies of lithium-containing oxides at high temperature

    Science.gov (United States)

    Ikeda, Yasushi; Tamaki, Masayoshi; Matsumoto, Genichi; Amioka, Kenji; Mizuno, Tomoyasu

    The sublimation and vaporization of various lithium containing oxides have been studied by high temperature mass spectrometry. The installed Knudsen cell apparatus gave some useful information about the vapor species, appearance potentials, partial pressures and heats of reactions involved. The investigated oxides are Li 2O, Li 2O-Al 2O 3, Li 2O-MoO 2 and Li 2O-SiO 2 systems. This paper mainly presents the most recent data for the Li 2O-SiO 2 system. A relationship for the decomposition reaction of ortho-Li 4SiO 4 was deduced. The heat of the reaction was determined by the third law method. The activity of the Li 2O component in the double oxides was estimated from the partial pressures of the vapor species. γ-LiAlO 2 and meta-Li 2SiO 3 showed fairly low activities in comparison with Li 2O oxide. The activity coefficients decreased with the Li 2O mole fraction in the lithium compounds. The heats of formation and atomization of LiO and Li 2O gaseous species were determined.

  3. Lithium Thiophosphate Compounds as Stable High Rate Li-Ion Separators

    Energy Technology Data Exchange (ETDEWEB)

    Apblett, Christopher A. [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States)

    2014-09-01

    Battery separators based upon lithium thiophosphate (LiPS4) have previously been demonstrated at UC Boulder, but the thickness of the separators was too high to be of practical use in a lithium ion battery. The separators are solid phase, which makes them intrinsically less prone to thermal runaway and thereby improves safety. Results of attempting to develop sputtered thin film layers of this material by starting with targets of pure Li, Li2S, and P2S5 are reported. Sputtering rates and film quality and composition are discussed, along with efforts to use Raman spectroscopy to determine quantitative film composition. The latter is a rate limiting step in the investigation of these films, as they are typically thin and require long times to get to sufficient thickness to be analyzed using traditional methods, whereas Raman is particularly well suited to this analysis, if it can be made quantitative. The final results of the film deposition methods are reported, and a path towards new films is discussed. Finally, it should be noted that this program originally began with one graduate student working on the program, but this student ultimately chose to not continue with a PhD. A second student took over in the middle of the effort, and a new program has been proposed with a significantly altered chemistry to take the program in a new direction.

  4. Facile fabrication of Si mesoporous nanowires for high-capacity and long-life lithium storage

    Science.gov (United States)

    Chen, Jizhang; Yang, Li; Rousidan, Saibihai; Fang, Shaohua; Zhang, Zhengxi; Hirano, Shin-Ichi

    2013-10-01

    Si has the second highest theoretical capacity among all the known anode materials for lithium ion batteries, whereas it is vulnerable to pulverization and crumbling upon lithiation/delithiation. Herein, Si mesoporous nanowires prepared by a scalable and cost-effective procedure are reported for the first time. Such nanowire morphology and mesoporous structure can effectively buffer the huge lithiation-induced volume expansion of Si, therefore contributing to excellent cycling stability and high-rate capability. Reversible capacities of 1826.8 and 737.4 mA h g-1 can be obtained at 500 mA g-1 and a very high current density of 10 A g-1, respectively. After 1000 cycles at 2500 mA g-1, this product still maintains a high capacity of 643.5 mA h g-1.Si has the second highest theoretical capacity among all the known anode materials for lithium ion batteries, whereas it is vulnerable to pulverization and crumbling upon lithiation/delithiation. Herein, Si mesoporous nanowires prepared by a scalable and cost-effective procedure are reported for the first time. Such nanowire morphology and mesoporous structure can effectively buffer the huge lithiation-induced volume expansion of Si, therefore contributing to excellent cycling stability and high-rate capability. Reversible capacities of 1826.8 and 737.4 mA h g-1 can be obtained at 500 mA g-1 and a very high current density of 10 A g-1, respectively. After 1000 cycles at 2500 mA g-1, this product still maintains a high capacity of 643.5 mA h g-1. Electronic supplementary information (ESI) available: SEM images; N2 adsorption/desorption isotherm; long-term cycling performance at 500 mA g-1 comparison with other literature. See DOI: 10.1039/c3nr03955b

  5. Toward practical application of functional conductive polymer binder for a high-energy lithium-ion battery design.

    Science.gov (United States)

    Zhao, Hui; Wang, Zhihui; Lu, Peng; Jiang, Meng; Shi, Feifei; Song, Xiangyun; Zheng, Ziyan; Zhou, Xin; Fu, Yanbao; Abdelbast, Guerfi; Xiao, Xingcheng; Liu, Zhi; Battaglia, Vincent S; Zaghib, Karim; Liu, Gao

    2014-11-12

    Silicon alloys have the highest specific capacity when used as anode material for lithium-ion batteries; however, the drastic volume change inherent in their use causes formidable challenges toward achieving stable cycling performance. Large quantities of binders and conductive additives are typically necessary to maintain good cell performance. In this report, only 2% (by weight) functional conductive polymer binder without any conductive additives was successfully used with a micron-size silicon monoxide (SiO) anode material, demonstrating stable and high gravimetric capacity (>1000 mAh/g) for ∼500 cycles and more than 90% capacity retention. Prelithiation of this anode using stabilized lithium metal powder (SLMP) improves the first cycle Coulombic efficiency of a SiO/NMC full cell from ∼48% to ∼90%. The combination enables good capacity retention of more than 80% after 100 cycles at C/3 in a lithium-ion full cell.

  6. Superior electrochemical performance of sulfur/graphene nanocomposite material for high-capacity lithium-sulfur batteries.

    Science.gov (United States)

    Wang, Bei; Li, Kefei; Su, Dawei; Ahn, Hyojun; Wang, Guoxiu

    2012-06-01

    Sulfur/graphene nanocomposite material has been prepared by incorporating sulfur into the graphene frameworks through a melting process. Field-emission scanning electron microscope analysis shows a homogeneous distribution of sulfur in the graphene nanosheet matrix. The sulfur/graphene nanocomposite exhibits a super-high lithium-storage capacity of 1580 mA h g(-1) and a satisfactory cycling performance in lithium-sulfur cells. The enhancement of the reversible capacity and cycle life could be attributed to the flexible graphene nanosheet matrix, which acts as a conducting medium and a physical buffer to cushion the volume change of sulfur during the lithiation and delithiation process. Graphene-based nanocomposites can significantly improve the electrochemical performance of lithium-sulfur batteries.

  7. Highly Stable Operation of Lithium Metal Batteries Enabled by the Formation of a Transient High Concentration Electrolyte Layer

    Energy Technology Data Exchange (ETDEWEB)

    Zheng, Jianming; Yan, Pengfei; Mei, Donghai; Engelhard, Mark H.; Cartmell, Samuel S.; Polzin, Bryant; Wang, Chong M.; Zhang, Jiguang; Xu, Wu

    2016-02-08

    Lithium (Li) metal has been extensively investigated as an anode for rechargeable battery applications due to its ultrahigh specific capacity and the lowest redox potential. However, significant challenges including dendrite growth and low Coulombic efficiency are still hindering the practical applications of rechargeable Li metal batteries. Here, we demonstrate that long-term cycling of Li metal batteries can be realized by the formation of a transient high concentration electrolyte layer near the surface of Li metal anode during high rate discharge process. The highly concentrated Li+ ions in this transient layer will immediately solvate with the available solvent molecules and facilitate the formation of a stable and flexible SEI layer composed of a poly(ethylene carbonate) framework integrated with other organic/inorganic lithium salts. This SEI layer largely suppresses the corrosion of Li metal anode by free organic solvents and enables the long-term operation of Li metal batteries. The fundamental findings in this work provide a new direction for the development and operation of Li metal batteries that could be operated at high current densities for a wide range of applications.

  8. Highly nitrogen-doped carbon capsules: scalable preparation and high-performance applications in fuel cells and lithium ion batteries.

    Science.gov (United States)

    Hu, Chuangang; Xiao, Ying; Zhao, Yang; Chen, Nan; Zhang, Zhipan; Cao, Minhua; Qu, Liangti

    2013-04-07

    Highly nitrogen-doped carbon capsules (hN-CCs) have been successfully prepared by using inexpensive melamine and glyoxal as precursors via solvothermal reaction and carbonization. With a great promise for large scale production, the hN-CCs, having large surface area and high-level nitrogen content (N/C atomic ration of ca. 13%), possess superior crossover resistance, selective activity and catalytic stability towards oxygen reduction reaction for fuel cells in alkaline medium. As a new anode material in lithium-ion battery, hN-CCs also exhibit excellent cycle performance and high rate capacity with a reversible capacity of as high as 1046 mA h g(-1) at a current density of 50 mA g(-1) after 50 cycles. These features make the hN-CCs developed in this study promising as suitable substitutes for the expensive noble metal catalysts in the next generation alkaline fuel cells, and as advanced electrode materials in lithium-ion batteries.

  9. Solid-state lithium battery

    Science.gov (United States)

    Ihlefeld, Jon; Clem, Paul G; Edney, Cynthia; Ingersoll, David; Nagasubramanian, Ganesan; Fenton, Kyle Ross

    2014-11-04

    The present invention is directed to a higher power, thin film lithium-ion electrolyte on a metallic substrate, enabling mass-produced solid-state lithium batteries. High-temperature thermodynamic equilibrium processing enables co-firing of oxides and base metals, providing a means to integrate the crystalline, lithium-stable, fast lithium-ion conductor lanthanum lithium tantalate (La.sub.1/3-xLi.sub.3xTaO.sub.3) directly with a thin metal foil current collector appropriate for a lithium-free solid-state battery.

  10. Characteristics of free-surface wave on high-speed liquid lithium jet for IFMIF

    Energy Technology Data Exchange (ETDEWEB)

    Kanemura, Takuji, E-mail: kanemura@stu.nucl.eng.osaka-u.ac.jp [Osaka University, 2-1 Yamada-oka, Suita, Osaka 565-0871 (Japan); Yoshihashi-Suzuki, Sachiko [Osaka University, 2-1 Yamada-oka, Suita, Osaka 565-0871 (Japan); Kondo, Hiroo [Japan Atomic Energy Agency, 2-4 Shirane Shirakata, Tokai-mura, Naka-gun, Ibaraki 319-1195 (Japan); Sugiura, Hirokazu; Yamaoka, Nobuo [Osaka University, 2-1 Yamada-oka, Suita, Osaka 565-0871 (Japan); Ida, Mizuho; Nakamura, Hiroo [Japan Atomic Energy Agency, 2-4 Shirane Shirakata, Tokai-mura, Naka-gun, Ibaraki 319-1195 (Japan); Matsushita, Izuru [Mitsubishi Heavy Industries Mechatronics Systems, Ltd., 1-16 5-chome, Komatsu-dori, Hyogo-ku, Kobe, Hyogo 652-0865 (Japan); Muroga, Takeo [National Institute for Fusion Science, 322-6 Oroshicho, Toki, Gifu 509-5292 (Japan); Horiike, Hiroshi [Osaka University, 2-1 Yamada-oka, Suita, Osaka 565-0871 (Japan)

    2011-10-01

    The characteristics of the surface waves on a high-speed liquid lithium wall jet were examined in a Li circulation loop at Osaka University for the International Fusion Materials Irradiation Facility (IFMIF). Surface fluctuations were measured by a contact-type liquid level sensor at 175 mm downstream from the nozzle exit, which corresponds to the deuteron beam's axis in the IFMIF, and observed with a high-speed video (HSV) camera. Both the observation and measurement results indicated that the surface fluctuations were composed of various scale turbulent fluctuations. The measurement results especially showed good agreement with the log-normal distribution which is one of the turbulent intermittency theories. The dominant wavelength was found to be shorter with increase in the flow velocity, and reached approximately 4 mm at the velocity of 15 m/s, which gave close agreement with the visually observed wavelength.

  11. Phosphorus-doped silicon nanorod anodes for high power lithium-ion batteries

    Directory of Open Access Journals (Sweden)

    Chao Yan

    2017-01-01

    Full Text Available Heavy-phosphorus-doped silicon anodes were fabricated on CuO nanorods for application in high power lithium-ion batteries. Since the conductivity of lithiated CuO is significantly better than that of CuO, after the first discharge, the voltage cut-off window was then set to the range covering only the discharge–charge range of Si. Thus, the CuO core was in situ lithiated and acts merely as the electronic conductor in the following cycles. The Si anode presented herein exhibited a capacity of 990 mAh/g at the rate of 9 A/g after 100 cycles. The anode also presented a stable rate performance even at a current density as high as 20 A/g.

  12. High-Yield Lithium-Injection Fusion-Energy (HYLIFE) reactor

    Energy Technology Data Exchange (ETDEWEB)

    Blink, J.A.; Hogam, W.J.; Hovingh, J.; Meier, E.R.; Pitts, J.H. (comps.)

    1985-12-23

    The High-Yield Lithium-Injection Fusion Energy (HYLIFE) concept to convent inertial confinement fusion energy into electric power has undergone intensive research and refinement at LLNL since 1978. This paper reports on the final HYLIFE design, focusing on five major areas: the HYLIFE reaction chamber (which includes neutronics, liquid-metal jet-array hydrocynamics, and structural design), supporting systems, primary steam system and balance of plant, safety and environmental protection, and costs. An annotated bibliography of reports applicable to HYLIFE is also provided. We conclude that HYLIFE is a particularly viable concept for the safe, clean production of electrical energy. The liquid-metal jet array, HYLIFE's key design feature, protects the surrounding structural components from x-rays, fusion fuel-pellet debris, neutron damage and activation, and high temperatures and stresses, allowing the structure to last for the plant's entire 30-year lifetime without being replaced. 127 refs., 18 figs.

  13. A single lithium-ion battery protection circuit with high reliability and low power consumption

    Institute of Scientific and Technical Information of China (English)

    Jiang Jinguang; Li Sen

    2014-01-01

    A single lithium-ion battery protection circuit with high reliability and low power consumption is proposed.The protection circuit has high reliability because the voltage and current of the battery are controlled in a safe range.The protection circuit can immediately activate a protective function when the voltage and current of the battery are beyond the safe range.In order to reduce the circuit's power consumption,a sleep state control circuit is developed.Additionally,the output frequency of the ring oscillation can be adjusted continuously and precisely by the charging capacitors and the constant-current source.The proposed protection circuit is fabricated in a 0.5 μm mixed-signal CMOS process.The measured reference voltage is 1.19 V,the overvoltage is 4.2 V and the undervoltage is 2.2 V.The total power is about 9μW.

  14. Graphene-wrapped CoS nanoparticles for high-capacity lithium-ion storage.

    Science.gov (United States)

    Gu, Yan; Xu, Yi; Wang, Yong

    2013-02-01

    Graphene-wrapped CoS nanoparticles are synthesized by a solvothermal approach. The product is significantly different from porous CoS microspheres prepared in the absence of graphene under similar preparation conditions. The CoS microspheres and CoS/graphene composite are fabricated as anode materials for lithium-ion batteries. The CoS/graphene composite is found to be better suitable as an anode in terms of higher capacity and better cycling performances. The nanocomposite exhibits an unprecedented high reversible capacity of 1056 mA h/g among all cobalt sulfide-based anode materials. Good cycling performances are also observed at both small and high current rates.

  15. High Cycle Life, Low Temperature Lithium Ion Battery for Earth Orbiting and Planetary Missions Project

    Data.gov (United States)

    National Aeronautics and Space Administration — NASA requires development of advanced rechargeable electrochemical battery systems for lithium ion batteries to support orbiting spacecraft and planetary missions....

  16. Shielding design for PWR in France

    Energy Technology Data Exchange (ETDEWEB)

    Champion, G.; Charransol; Le Dieu de Ville, A.; Nimal, J.C.; Vergnaud, T.

    1983-05-01

    Shielding calculation scheme used in France for PWR is presented here for 900 MWe and 1300 MWe plants built by EDF the French utility giving electricity. Neutron dose rate at areas accessible by personnel during the reactor operation is calculated and compared with the measurements which were carried out in 900 MWe units up to now. Measurements on the first French 1300 MWe reactor are foreseen at the end of 1983.

  17. The integrated PWR; Les REP integres

    Energy Technology Data Exchange (ETDEWEB)

    Gautier, G.M. [CEA Cadarache, 13 - Saint-Paul-lez-Durance (France). Dept. d' Etudes des Reacteurs

    2002-07-01

    This document presents the integrated reactors concepts by a presentation of four reactors: PIUS, SIR, IRIS and CAREM. The core conception, the operating, the safety, the economical aspects and the possible users are detailed. From the performance of the classical integrated PWR, the necessity of new innovative fuels utilization, the research of a simplified design to make easier the safety and the KWh cost decrease, a new integrated reactor is presented: SCAR 600. (A.L.B.)

  18. Improving reversible capacities of high-surface lithium insertion materials – the case of amorphous TiO2

    NARCIS (Netherlands)

    Ganapathy, S.; Basak, S.; Lefering, A.; Rogers, E.; Zandbergen, H.W.; Wagemaker, M.

    2014-01-01

    Chemisorbed water and solvent molecules and their reactivity with components from the electrolyte in high-surface nano-structured electrodes remains a contributing factor toward capacity diminishment on cycling in lithium ion batteries due to the limit in maximum annealing temperature. Here, we repo

  19. Metal hydride-based materials towards high performance negative electrodes for all-solid-state lithium-ion batteries.

    Science.gov (United States)

    Zeng, Liang; Kawahito, Koji; Ikeda, Suguru; Ichikawa, Takayuki; Miyaoka, Hiroki; Kojima, Yoshitsugu

    2015-06-18

    Electrode performances of MgH2-LiBH4 composite materials for lithium-ion batteries have been studied using LiBH4 as the solid-state electrolyte, which shows a high reversible capacity of 1650 mA h g(-1) with an extremely low polarization of 0.05 V, durable cyclability and robust rate capability.

  20. Lithium-cyclo-difluoromethane-1,1-bis(sulfonyl)imide as a stabilizing electrolyte additive for improved high voltage applications in lithium-ion batteries.

    Science.gov (United States)

    Murmann, Patrick; Streipert, Benjamin; Kloepsch, Richard; Ignatiev, Nikolai; Sartori, Peter; Winter, Martin; Cekic-Laskovic, Isidora

    2015-04-14

    Lithium-cyclo-difluoromethane-1,1-bis(sulfonyl)imide (LiDMSI) was evaluated as an electrolyte additive in lithium-ion batteries for improved high voltage applications. Cycling the cathode at high potentials leads to the electrochemical oxidation of the salt to form a cathode electrolyte interphase (CEI) layer on the cathode surface. With the addition of 2 wt% of LiDMSI to the 1 M LiPF6 in 1 : 1 (by wt) EC : DEC electrolyte, the capacity retention and the Coulombic efficiency in LiNi1/3Co1/3Mn1/3O2/Li-half-cells as well as in LiNi1/3Co1/3Mn1/3O2/graphite-full-cells were improved. The cycling results point out the less over-potential and resistance at the cathode/electrolyte interface. These improvements are studied by SEM, EIS and XPS techniques.

  1. New approaches for high energy density lithium-sulfur battery cathodes.

    Science.gov (United States)

    Evers, Scott; Nazar, Linda F

    2013-05-21

    The goal of replacing combustion engines or reducing their use presents a daunting problem for society. Current lithium-ion technologies provide a stepping stone for this dramatic but inevitable change. However, the theoretical gravimetric capacity (∼300 mA h g(-1)) is too low to overcome the problems of limited range in electric vehicles, and their cost is too high to sustain the commercial viability of electrified transportation. Sulfur is the one of the most promising next generation cathode materials. Since the 1960s, researchers have studied sulfur as a cathode, but only recently have great strides been made in preparing viable composites that can be used commercially. Sulfur batteries implement inexpensive, earth-abundant elements at the cathode while offering up to a five-fold increase in energy density compared with present Li-ion batteries. Over the past few years, researchers have come closer to solving the challenges associated with the sulfur cathode. Using carbon or conducting polymers, researchers have wired up sulfur, an excellent insulator, successfully. These conductive hosts also function to encapsulate the active sulfur mass upon reduction/oxidation when highly soluble lithium polysulfides are formed. These soluble discharge products remain a crux of the Li-S cell and need to be contained in order to increase cycle life and capacity retention. The use of mesoporous carbons and tailored designs featuring porous carbon hollow spheres have led to highly stable discharge capacities greater than 900 mA h g(-1) over 100 cycles. In an attempt to fully limit polysulfide dissolution, methods that rely on coating carbon/sulfur composites with polymers have led to surprisingly stable capacities (∼90% of initial capacity retained). Additives will also play an important role in sulfur electrode design. For example, small fractions (> 3 wt%) of porous silica or titania effectively act as polysulfide reservoirs, decreasing their concentration in the

  2. Assessment of void swelling in austenitic stainless steel PWR core internals.

    Energy Technology Data Exchange (ETDEWEB)

    Chung, H. M.; Energy Technology

    2006-01-31

    As many pressurized water reactors (PWRs) age and life extension of the aged plants is considered, void swelling behavior of austenitic stainless steel (SS) core internals has become the subject of increasing attention. In this report, the available database on void swelling and density change of austenitic SSs was critically reviewed. Irradiation conditions, test procedures, and microstructural characteristics were carefully examined, and key factors that are important to determine the relevance of the database to PWR conditions were evaluated. Most swelling data were obtained from steels irradiated in fast breeder reactors at temperatures >385 C and at dose rates that are orders of magnitude higher than PWR dose rates. Even for a given irradiation temperature and given steel, the integral effects of dose and dose rate on void swelling should not be separated. It is incorrect to extrapolate swelling data on the basis of 'progressive compounded multiplication' of separate effects of factors such as dose, dose rate, temperature, steel composition, and fabrication procedure. Therefore, the fast reactor data should not be extrapolated to determine credible void swelling behavior for PWR end-of-life (EOL) or life-extension conditions. Although the void swelling data extracted from fast reactor studies is extensive and conclusive, only limited amounts of swelling data and information have been obtained on microstructural characteristics from discharged PWR internals or steels irradiated at temperatures and at dose rates comparable to those of a PWR. Based on this relatively small amount of information, swelling in thin-walled tubes and baffle bolts in a PWR is not considered a concern. As additional data and relevant research becomes available, the newer results should be integrated with existing data, and the worthiness of this conclusion should continue to be scrutinized. PWR baffle reentrant corners are the most likely location to experience high swelling

  3. Activity transport models for PWR primary circuits; PWR-ydinvoimalaitoksen primaeaeripiirin aktiivisuuskulkeutumismallit

    Energy Technology Data Exchange (ETDEWEB)

    Tanner, V.; Rosenberg, R. [VTT Chemical Technology, Otaniemi (Finland)

    1995-03-01

    The corrosion products activated in the primary circuit form a major source of occupational radiation dose in the PWR reactors. Transport of corrosion activity is a complex process including chemistry, reactor physics, thermodynamics and hydrodynamics. All the mechanisms involved are not known and there is no comprehensive theory for the process, so experimental test loops and plant data are very important in research efforts. Several activity transport modelling attempts have been made to improve the water chemistry control and to minimise corrosion in PWR`s. In this research report some of these models are reviewed with special emphasis on models designed for Soviet VVER type reactors. (51 refs., 16 figs., 4 tabs.).

  4. Sandwich-like heat-resistance composite separators with tunable pore structure for high power high safety lithium ion batteries

    Science.gov (United States)

    Shi, Junli; Shen, Tao; Hu, Huasheng; Xia, Yonggao; Liu, Zhaoping

    2014-12-01

    We demonstrate a new kind of composite separators. A unique feature of the separators is the three-tier structure, i.e. the crosslinked polyethylene glycol (PEG) skin layer being formed on both sides of the nonwoven separators by in-situ polymerization and the large pores in the interior of the nonwoven separators being remained. The surface pore structure and the thickness of the skin layer could be adjusted by controlling the concentration of the coating solution. The skin layer is proved to be able to provide internal short circuit protection, to contribute a more stable interfacial resistance and to alleviate liquid electrolyte leakage effectively, yielding an excellent cyclability. The remained large pores in the interior of the composite separators could provide an access for the fast transportation of lithium ions, giving rise to a very high ion conductivity. The polyimide (PI) nonwoven is employed to ensure enhanced thermal stability of the composite separators. More notably, the composite separators fabricated from the coating solution with a composition ratio of 20 wt% provide superior cell performances owing to the well-tailored microporous structure, comparing with the commercialized polypropylene (PP) separator, which show great promise for the application in the high power lithium ion batteries.

  5. Lithium carbonate as an electrolyte additive for enhancing the high-temperature performance of lithium manganese oxide spinel cathode

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Renheng [School of Metallurgy and Environment, Central South University, Changsha 410083 (China); Li, Xinhai, E-mail: 703131039@qq.com [School of Metallurgy and Environment, Central South University, Changsha 410083 (China); Wang, Zhixing; Guo, Huajun [School of Metallurgy and Environment, Central South University, Changsha 410083 (China); Hou, Tao [Jiangxi Youli New Materials Co., Ltd, Pingxiang 337000 (China); Yan, Guochun; Huang, Bin [School of Metallurgy and Environment, Central South University, Changsha 410083 (China)

    2015-01-05

    Highlights: • The addition of Li{sub 2}CO{sub 3} to the electrolyte can suppress the contents of HF in the electrolyte. • The low self-discharge rate of the LiMn{sub 2}O{sub 4} cells with Li{sub 2}CO{sub 3} is lower than that of no additive. • The LiMn{sub 2}O{sub 4} cells with Li{sub 2}CO{sub 3} exhibit better rate capability and excellent cycle stability than that without Li{sub 2}CO{sub 3}. • A stable film can be formed on the LiMn{sub 2}O{sub 4} cathode using containing-Li{sub 2}CO{sub 3} electrolyte. - Abstract: The effect of lithium carbonate (Li{sub 2}CO{sub 3}) as an additive on the stability of the electrolyte and cycling performance of lithium manganese oxide spinel (LiMn{sub 2}O{sub 4}) batteries at elevated temperature was studied. The addition of Li{sub 2}CO{sub 3} to the electrolyte can suppress the capacity fading of LiMn{sub 2}O{sub 4} batteries. The linear sweep voltammetry (LSV) and the cyclic voltammetry (CV) indicate that Li{sub 2}CO{sub 3} has a lower oxidation potential in the mixed solvents of ethylene carbonate (EC), diethyl carbonate (DEC) and ethyl methyl carbonate (EMC), participating in the formation process of the stable cathode electrolyte interface (CEI) film. In addition, the results of electrochemical impedance spectroscopy (EIS), scanning electron microscopy (SEM) and transmission electron microscopy (TEM) demonstrate that the stable CEI film of the cells with Li{sub 2}CO{sub 3} can be formed, which can effectively reduce the dissolution of Mn{sup 2+} from LiMn{sub 2}O{sub 4} into the electrolyte at elevated temperature. It is concluded that the addition of Li{sub 2}CO{sub 3} to a solution of 1 M LiPF{sub 6}–EC/EMC/DEC = 1/1/1 (weight ratio) may decrease solvent decomposition and change the structure of the passivation film on the LiMn{sub 2}O{sub 4} cathode.

  6. A novel quasi-solid state electrolyte with highly effective polysulfide diffusion inhibition for lithium-sulfur batteries

    Science.gov (United States)

    Zhong, Hai; Wang, Chunhua; Xu, Zhibin; Ding, Fei; Liu, Xinjiang

    2016-05-01

    Polymer solid state electrolytes are actively sought for their potential application in energy storage devices, particularly lithium metal rechargeable batteries. Herein, we report a polymer with high concentration salts as a quasi-solid state electrolyte used for lithium-sulfur cells, which shows an ionic conductivity of 1.6 mS cm-1 at room temperature. The cycling performance of Li-S battery with this electrolyte shows a long cycle life (300 cycles) and high coulombic efficiency (>98%), without any consuming additives in the electrolyte. Moreover, it also shows a remarkably decreased self-discharge (only 0.2%) after storage for two weeks at room temperature. The reason can be attributed to that the electrolyte can suppress polysulfide anions diffusion, due to the high ratio oxygen atoms with negative charges which induce an electrical repulsion to the polysulfide anions, and their relatively long chains which can provide additional steric hindrance. Thus, the polysulfide anions can be located around carbon particles, which result in remarkably improved overall electrochemical performance, and also the electrolyte have a function of suppress the formation of lithium dendrites on the lithium anode surface.

  7. Fabrication of cermet bearings for the control system of a high temperature lithium cooled nuclear reactor

    Science.gov (United States)

    Yacobucci, H. G.; Heestand, R. L.; Kizer, D. E.

    1973-01-01

    The techniques used to fabricate cermet bearings for the fueled control drums of a liquid metal cooled reference-design reactor concept are presented. The bearings were designed for operation in lithium for as long as 5 years at temperatures to 1205 C. Two sets of bearings were fabricated from a hafnium carbide - 8-wt. % molybdenum - 2-wt. % niobium carbide cermet, and two sets were fabricated from a hafnium nitride - 10-wt. % tungsten cermet. Procedures were developed for synthesizing the material in high purity inert-atmosphere glove boxes to minimize oxygen content in order to enhance corrosion resistance. Techniques were developed for pressing cylindrical billets to conserve materials and to reduce machining requirements. Finishing was accomplished by a combination of diamond grinding, electrodischarge machining, and diamond lapping. Samples were characterized in respect to composition, impurity level, lattice parameter, microstructure and density.

  8. Raspberry-like Nanostructured Silicon Composite Anode for High-Performance Lithium-Ion Batteries.

    Science.gov (United States)

    Fang, Shan; Tong, Zhenkun; Nie, Ping; Liu, Gao; Zhang, Xiaogang

    2017-06-07

    Adjusting the particle size and nanostructure or applying carbon materials as the coating layers is a promising method to hold the volume expansion of Si for its practical application in lithium-ion batteries (LIBs). Herein, the mild carbon coating combined with a molten salt reduction is precisely designed to synthesize raspberry-like hollow silicon spheres coated with carbon shells (HSi@C) as the anode materials for LIBs. The HSi@C exhibits a remarkable electrochemical performance; a high reversible specific capacity of 886.2 mAh g(-1) at a current density of 0.5 A g(-1) after 200 cycles is achieved. Moreover, even after 500 cycles at a current density of 2.0 A g(-1), a stable capacity of 516.7 mAh g(-1) still can be obtained.

  9. In Situ High Resolution Synchrotron X-Ray Powder Diffraction Studies of Lithium Batteries

    DEFF Research Database (Denmark)

    Amri, Mahrez; Fitch, Andy; Norby, Poul

    2015-01-01

    . They will be used not only for transportation, but also for medium and short term storage as well as for frequency stabilization in intermittent grid scale energy sources such as solar and wind. Thus, the development of new cheaper and safer battery materials with high energy and power density is very important......Lithium ion battery technology is the heart in operating modern technology devices such as mobile phones and laptops. However, as our society is moving towards the utilization of sustainable energy sources, batteries can be foreseen to become an even more important part of the energy infrastructure...... for a successful worldwide energy transition. The understanding of structural and compositional changes of bulk electrodes in batteries is undoubtedly important. However, it is often transport of electrons and ions across and through interfaces [1] (e.g., between lithiated and delithiated domains) which limits...

  10. Study of Stable Cathodes and Electrolytes for High Specific Density Lithium-Air Battery

    Science.gov (United States)

    Hernandez-Lugo, Dionne M.; Wu, James; Bennett, William; Ming, Yu; Zhu, Yu

    2015-01-01

    Future NASA missions require high specific energy battery technologies, greater than 400 Wh/kg. Current NASA missions are using "state-of-the-art" (SOA) Li-ion batteries (LIB), which consist of a metal oxide cathode, a graphite anode and an organic electrolyte. NASA Glenn Research Center is currently studying the physical and electrochemical properties of the anode-electrolyte interface for ionic liquid based Li-air batteries. The voltage-time profiles for Pyr13FSI and Pyr14TFSI ionic liquids electrolytes studies on symmetric cells show low over-potentials and no dendritic lithium morphology. Cyclic voltammetry measurements indicate that these ionic liquids have a wide electrochemical window. As a continuation of this work, sp2 carbon cathode and these low flammability electrolytes were paired and the physical and electrochemical properties were studied in a Li-air battery system under an oxygen environment.

  11. PWR reactor vessel in-service-inspection according to RSEM

    Energy Technology Data Exchange (ETDEWEB)

    Algarotti, Marc; Dubois, Philippe; Hernandez, Luc; Landez, Jean Paul [Intercontrole, 13, rue du Capricorne - SILIC 433, 94583 Rungis - Cedex (France)

    2006-07-01

    Nuclear services experience Framatome ANP (an AREVA and Siemens company) has designed and constructed 86 Pressurized Water Reactors (PWR) around the world including the three units lately commissioned at Ling Ao in the People's Republic of China and ANGRA 2 in Brazil; the company provided general and specialized outage services supporting numerous outages. Along with the American and German subsidiaries, Framatome ANP Inc. and Framatome ANP GmbH, Framatome ANP is among the world leading nuclear services providers, having experience of over 500 PWR outages on 4 continents, with current involvement in more than 50 PWR outages per year. Framatome ANP's experience in the examinations of reactor components began in the 1970's. Since then, each unit (American, French and German companies) developed automated NDT inspection systems and carried out pre-service and ISI (In-Service Inspections) using a large range of NDT techniques to comply with each utility expectations. These techniques have been validated by the utilities and the safety authorities of the countries where they were implemented. Notably Framatome ANP is fully qualified to provide full scope ISI services to satisfy ASME Section XI requirements, through automated NDE tasks including nozzle inspections, reactor vessel head inspections, steam generator inspections, pressurizer inspections and RPV (Reactor Pressure Vessel) inspections. Intercontrole (Framatome ANP subsidiary dedicated in supporting ISI) is one of the leading NDT companies in the world. Its main activity is devoted to the inspection of the reactor primary circuit in French and foreign PWR Nuclear Power Plants: the reactor vessel, the steam generators, the pressurizer, the reactor internals and reactor coolant system piping. NDT methods mastered by Intercontrole range from ultrasonic testing to eddy current and gamma ray examinations, as well as dye penetrant testing, acoustic monitoring and leak testing. To comply with the high

  12. High-rate lithium-sulfur batteries promoted by reduced graphene oxide coating.

    Science.gov (United States)

    Li, Nianwu; Zheng, Mingbo; Lu, Hongling; Hu, Zibo; Shen, Chenfei; Chang, Xiaofeng; Ji, Guangbin; Cao, Jieming; Shi, Yi

    2012-04-28

    Lithium-sulfur batteries have a poor rate performance and low cycle stability due to the shuttling loss of intermediate lithium polysulfides. To address this issue, a carbon-sulfur nanocomposite coated with reduced graphene oxide was designed to confine the polysulfides.

  13. Development and analysis of a lithium carbon monofluoride battery-lithium ion capacitor hybrid system for high pulse-power applications

    Science.gov (United States)

    Smith, Patricia H.; Sepe, Raymond B.; Waterman, Kyle G.; Myron, L. Jeff

    2016-09-01

    Although Li/CFx and Li/CFxMnO2 have two of the highest energy densities of all commercial lithium primary batteries known to date, they are typically current-limited and therefore are not used in high-power applications. In this work, a Li/CFxMnO2 battery (BA-5790) was hybridized with a 1000 F lithium ion capacitor to allow its use for portable electronic devices requiring 100 W 1-min pulses. An intelligent, power-management board was developed for managing the energy flow between the components. The hybrid architecture was shown to maintain the battery current to a level that minimized energy loss and thermal stress. The performance of the Li/CFxMnO2 hybrid was compared to the standard Li/SO2 battery (BA-5590). The hybrid was shown to deliver the same number of 100 W pulse cycles as two BA-5590 batteries, resulting in a weight savings of 30% and a volumetric reduction of 20%. For devices requiring 8 h of operational time or less, a 5-cell Li/CFxMnO2 hybrid was found to be a lighter (55%) and smaller (45%) power source than the existing two BA-5590 battery option, and a lighter (42%) and smaller (27%) option than 1½ BA-5790 batteries alone. At higher power requirements (>100 W), further weight and size improvements can be expected.

  14. Microwave exfoliated graphene oxide/TiO{sub 2} nanowire hybrid for high performance lithium ion battery

    Energy Technology Data Exchange (ETDEWEB)

    Ishtiaque Shuvo, Mohammad Arif; Rodriguez, Gerardo; Karim, Hasanul; Lin, Yirong [Department of Mechanical Engineering, University of Texas at El Paso, El Paso, Texas 79968 (United States); Islam, Md Tariqul; Noveron, Juan C. [Department of Chemistry, University of Texas at El Paso, El Paso, Texas 79968 (United States); Ramabadran, Navaneet [Department of Chemical Engineering, University of California at Santa Barbara, California 93106 (United States)

    2015-09-28

    Lithium ion battery (LIB) is a key solution to the demand of ever-improving, high energy density, clean-alternative energy systems. In LIB, graphite is the most commonly used anode material; however, lithium-ion intercalation in graphite is limited, hindering the battery charge rate and capacity. To date, one of the approaches in LIB performance improvement is by using porous carbon (PC) to replace graphite as anode material. PC's pore structure facilitates ion transport and has been proven to be an excellent anode material candidate in high power density LIBs. In addition, to overcome the limited lithium-ion intercalation obstacle, nanostructured anode assembly has been extensively studied to increase the lithium-ion diffusion rate. Among these approaches, high specific surface area metal oxide nanowires connecting nanostructured carbon materials accumulation have shown promising results for enhanced lithium-ion intercalation. Herein, we demonstrate a hydrothermal approach of growing TiO{sub 2} nanowires (TON) on microwave exfoliated graphene oxide (MEGO) to further improve LIB performance over PC. This MEGO-TON hybrid not only uses the high surface area of MEGO but also increases the specific surface area for electrode–electrolyte interaction. Therefore, this new nanowire/MEGO hybrid anode material enhances both the specific capacity and charge–discharge rate. Scanning electron microscopy and X-ray diffraction were used for materials characterization. Battery analyzer was used for measuring the electrical performance of the battery. The testing results have shown that MEGO-TON hybrid provides up to 80% increment of specific capacity compared to PC anode.

  15. Expanded graphite embedded with aluminum nanoparticles as superior thermal conductivity anodes for high-performance lithium-ion batteries.

    Science.gov (United States)

    Zhao, Tingkai; She, Shengfei; Ji, Xianglin; Guo, Xinai; Jin, Wenbo; Zhu, Ruoxing; Dang, Alei; Li, Hao; Li, Tiehu; Wei, Bingqing

    2016-09-27

    The development of high capacity and long-life lithium-ion batteries is a long-term pursuing and under a close scrutiny. Most of the researches have been focused on exploring electrode materials and structures with high store capability of lithium ions and at the same time with a good electrical conductivity. Thermal conductivity of an electrode material will also have significant impacts on boosting battery capacity and prolonging battery lifetime, which is, however, underestimated. Here, we present the development of an expanded graphite embedded with Al metal nanoparticles (EG-MNPs-Al) synthesized by an oxidation-expansion process. The synthesized EG-MNPs-Al material exhibited a typical hierarchical structure with embedded Al metal nanoparticles into the interspaces of expanded graphite. The parallel thermal conductivity was up to 11.6 W·m(-1)·K(-1) with a bulk density of 453 kg·m(-3) at room temperature, a 150% improvement compared to expanded graphite (4.6 W·m(-1)·K(-1)) owing to the existence of Al metal nanoparticles. The first reversible capacity of EG-MNPs-Al as anode material for lithium ion battery was 480 mAh·g(-1) at a current density of 100 mA·g(-1), and retained 84% capacity after 300 cycles. The improved cycling stability and system security of lithium ion batteries is attributed to the excellent thermal conductivity of the EG-MNPs-Al anodes.

  16. Expanded graphite embedded with aluminum nanoparticles as superior thermal conductivity anodes for high-performance lithium-ion batteries

    Science.gov (United States)

    Zhao, Tingkai; She, Shengfei; Ji, Xianglin; Guo, Xinai; Jin, Wenbo; Zhu, Ruoxing; Dang, Alei; Li, Hao; Li, Tiehu; Wei, Bingqing

    2016-09-01

    The development of high capacity and long-life lithium-ion batteries is a long-term pursuing and under a close scrutiny. Most of the researches have been focused on exploring electrode materials and structures with high store capability of lithium ions and at the same time with a good electrical conductivity. Thermal conductivity of an electrode material will also have significant impacts on boosting battery capacity and prolonging battery lifetime, which is, however, underestimated. Here, we present the development of an expanded graphite embedded with Al metal nanoparticles (EG-MNPs-Al) synthesized by an oxidation-expansion process. The synthesized EG-MNPs-Al material exhibited a typical hierarchical structure with embedded Al metal nanoparticles into the interspaces of expanded graphite. The parallel thermal conductivity was up to 11.6 W·m-1·K-1 with a bulk density of 453 kg·m-3 at room temperature, a 150% improvement compared to expanded graphite (4.6 W·m-1·K-1) owing to the existence of Al metal nanoparticles. The first reversible capacity of EG-MNPs-Al as anode material for lithium ion battery was 480 mAh·g-1 at a current density of 100 mA·g-1, and retained 84% capacity after 300 cycles. The improved cycling stability and system security of lithium ion batteries is attributed to the excellent thermal conductivity of the EG-MNPs-Al anodes.

  17. Fabrication of SnO2 Asymmetric Membranes for High Performance Lithium Battery Anode.

    Science.gov (United States)

    Wu, Ji; Chen, Hao; Byrd, Ian; Lovelace, Shavonne; Jin, Congrui

    2016-06-08

    Alloy electrode material like tin dioxide (SnO2) possesses much higher specific capacity as compared to commercial graphite anode in lithium ion battery (783 vs 372 mAh g(-1)). However, the huge volume change (260%) of SnO2-based anode during the alloying and dealloying process can cause significant electrode pulverization and rapid capacity loss. Herein we report the synthesis of SnO2 asymmetric membranes via a unique combination of phase inversion and sol-gel chemistry to overcome this big challenge. The SnO2 asymmetric membrane electrode demonstrates a specific capacity of 500 mAh g(-1) based on the overall electrode mass at a current density of 280 mA g(-1) (∼0.5C) with >96% capacity retention after 400 cycles. When the current density is increased from 28 to 560 mA g(-1), its overall capacity is only reduced by 36%. Such an outstanding rate and cycling performance is attributed to the existence of networking porous structure in the membrane that can provide high electrical conductivity, multiple diffusion channels, and free volumes for electrode expansion. The carbonization temperature has a dramatic impact on the electrode performance. Membranes carbonized at 500 °C show an excellent cycling performance, whereas the capacity of the membrane carbonized at 800 °C decreases by 51% in 100 cycles. Such a drastic difference in cycle life is caused by the reduction of small SnO2 NPs (∼3.9 nm) into large metallic tin spheres (∼40 nm) at 800 °C. This is the first original report on using asymmetric membrane structure to stabilize an SnO2-based lithium ion battery anode with an excellent electrochemical performance.

  18. Low-temperature lithium diffusion in simulated high-level boroaluminosilicate nuclear waste glasses

    Energy Technology Data Exchange (ETDEWEB)

    Neeway, James J.; Kerisit, Sebastien N.; Gin, Stephane; Wang, Zhaoying; Zhu, Zihua; Ryan, Joseph V.

    2014-12-01

    Ion exchange is recognized as an integral, if underrepresented, mechanism influencing glass corrosion. However, due to the formation of various alteration layers in the presence of water, it is difficult to conclusively deconvolute the mechanisms of ion exchange from other processes occurring simultaneously during corrosion. In this work, an operationally inert non-aqueous solution was used as an alkali source material to isolate ion exchange and study the solid-state diffusion of lithium. Specifically, the experiments involved contacting glass coupons relevant to the immobilization of high-level nuclear waste, SON68 and CJ-6, which contained Li in natural isotope abundance, with a non-aqueous solution of 6LiCl dissolved in dimethyl sulfoxide at 90 °C for various time periods. The depth profiles of major elements in the glass coupons were measured using time-of-flight secondary ion mass spectrometry (ToF-SIMS). Lithium interdiffusion coefficients, DLi, were then calculated based on the measured depth profiles. The results indicate that the penetration of 6Li is rapid in both glasses with the simplified CJ-6 glass (D6Li ≈ 4.0-8.0 × 10-21 m2/s) exhibiting faster exchange than the more complex SON68 glass (DLi ≈ 2.0-4.0 × 10-21 m2/s). Additionally, sodium ions present in the glass were observed to participate in ion exchange reactions; however, different diffusion coefficients were necessary to fit the diffusion profiles of the two alkali ions. Implications of the diffusion coefficients obtained in the absence of alteration layers to the long-term performance of nuclear waste glasses in a geological repository system are also discussed.

  19. Long term stability of Li-S batteries using high concentration lithium nitrate electrolytes

    Energy Technology Data Exchange (ETDEWEB)

    Adams, Brian DG; Carino, Emily V.; Connell, Justin G.; Han, Kee Sung; Cao, Ruiguo; Chen, Junzheng; Zheng, Jianming; Li, Qiuyan; Mueller, Karl T.; Henderson, Wesley A.; Zhang, Jiguang

    2017-09-08

    Lithium-sulfur (Li-S) battery is a very promising candidate for the next generation of energy storage systems required for electrical vehicles and grid energy storage applications due to its very high theoretical specific energy (2500 W h kg-1). However, the low coulombic efficiency (CE) during repeated Li plating/stripping of these processes have limited practical application of rechargeable Li-S batteries. In this work, a new electrolyte system based on high concentration of LiNO3 in diglyme solvent is developed which enables high CE of Li metal plating/stripping and high stability of Li anode in the sulfur containing electrolyte. Tailoring of electrolyte properties for the Li negative electrode has proven to be a successful strategy for improving the capacity retention and cycle life of Li-S batteries. This electrolyte provides a CE for Li plating/stripping of greater than 99% for over 200 cycles. In contrast, Li metal cycles for only less than 35 cycles at high CE in the standard 1 M LiTFSI + 2wt% LiNO3 in DOL:DME electrolyte under the same conditions. The stable Li metal anode enabled by the new electrolyte may accelerate the applications of high energy density Li-S batteries in both electrical vehicles and large-scale grid energy storage markets.

  20. High-performance ball-milled SiOx anodes for lithium ion batteries

    Science.gov (United States)

    Zhang, Junying; Zhang, Chunqian; Liu, Zhi; Zheng, Jun; Zuo, Yuhua; Xue, Chunlai; Li, Chuanbo; Cheng, Buwen

    2017-01-01

    High-performance SiOx was scalable synthesized by means of simple high-energy ball-milling method, and used as anode materials for lithium ion batteries. The electrochemical performance of SiOx electrode after high-energy ball-milling is improved effectively compared to raw SiOx. That is benefit for the reduced size of SiOx powder. By changing the species of conductive agents, improved cyclic performance and excellent rate capability were achieved. Under galvanostatic mode with current density of 0.3 A/g, SiOx electrode after high-energy ball-milling with optimized conductive agents delivers a reversible capacity of 1416.8 mAh/g with coulombic efficiency as high as 99.8% and capacity retention of 83.6% (1184.8 mAh/g) even after 100 cycles. The approach is simple and can be adopted for large scale production of high performance SiOx anode materials.

  1. Electric batteries. Lithium batteries; Piles electrique. Piles au lithium

    Energy Technology Data Exchange (ETDEWEB)

    Sarrazin, Ch. [Delegation Generale pour l' Armement, DGA/DRET, 75 - Paris (France)

    2002-05-01

    Lithium has the most negative potential and the highest mass capacity of all solid anode materials. It is the metal that allows to reach the highest mass energies in batteries when associated to a high potential cathode. The search for high performance cathodes has led to many different types of lithium batteries (transition metal oxides or sulfides, halogenides, oxi-halogenides, carbon, organic compounds etc..). These batteries can have a solid cathode (Li/CuO, Li/MnO{sub 2}, Li/CF{sub x}, etc..), or a liquid cathode (Li/SOCl{sub 2}, Li/SO{sub 2}, etc..) and in some cases they can have also a solid electrolyte, but not all types of lithium battery led to important industrial fabrication. The increasing use of lithium batteries is linked with the development of portable equipments for which, the compactness of the energy source is a key point. This article examines only the lithium batteries that have been the object of a significant industrial fabrication: lithium-sulfur dioxide, lithium-thionyl chloride, lithium-manganese dioxide, lithium-copper oxide, lithium-carbon fluoride, lithium-iron disulfide, other types of lithium batteries. (J.S.)

  2. Use of the anion gap and intermittent hemodialysis following continuous hemodiafiltration in extremely high dose acute-on-chronic lithium poisoning: A case report.

    Science.gov (United States)

    Komaru, Yohei; Inokuchi, Ryota; Ueda, Yoshihiro; Nangaku, Masaomi; Doi, Kent

    2017-08-10

    A 35-year-old woman intentionally took 40,000 mg of lithium carbonate, and she was transferred to our hospital with nausea, vomiting, and diarrhea. She was diagnosed as having bipolar disorder 10 years ago and was receiving oral lithium therapy. Blood test results on arrival were remarkable for a negative anion gap of -2.1 and later, the serum lithium level turned out to be as high as 15.4 mEq/L. Intubation was required because of disrupted consciousness, and continuous hemodiafiltration (CHDF) was immediately started in the intensive care unit to obtain constant removal of lithium. After adding intermittent hemodialysis (IHD) twice during the daytime to accelerate the lithium clearance, CHDF became unnecessary on day 4, and she was extubated on day 6 with complete recovery of consciousness. Close monitoring of the patient data showed recovery of the decreased anion gap as indicator of the serum lithium level reduction. On day 36, she was discharged without any complication and sequela. The current case highlighted the effective use of CHDF between IHD sessions to prevent the rebound elevation of lithium and the role of the anion gap as a surrogate marker of serum lithium concentration during the treatment. © 2017 International Society for Hemodialysis.

  3. Interface tracking simulations of bubbly flows in PWR relevant geometries

    Energy Technology Data Exchange (ETDEWEB)

    Fang, Jun, E-mail: jfang3@ncsu.edu [Department of Nuclear Engineering, North Carolina State University, Raleigh, NC 27695 (United States); Rasquin, Michel, E-mail: michel.rasquin@colorado.edu [Aerospace Engineering Department, University of Colorado, Boulder, CO 80309 (United States); Bolotnov, Igor A., E-mail: igor_bolotnov@ncsu.edu [Department of Nuclear Engineering, North Carolina State University, Raleigh, NC 27695 (United States)

    2017-02-15

    Highlights: • Simulations were performed for turbulent bubbly flows in PWR subchannel geometry. • Liquid turbulence is fully resolved by direct numerical simulation approach. • Bubble behavior is captured using level-set interface tracking method. • Time-averaged single- and two-phase turbulent flow statistical quantities are obtained. - Abstract: The advances in high performance computing (HPC) have allowed direct numerical simulation (DNS) approach coupled with interface tracking methods (ITM) to perform high fidelity simulations of turbulent bubbly flows in various complex geometries. In this work, we have chosen the geometry of the pressurized water reactor (PWR) core subchannel to perform a set of interface tracking simulations (ITS) with fully resolved liquid turbulence. The presented research utilizes a massively parallel finite-element based code, PHASTA, for the subchannel geometry simulations of bubbly flow turbulence. The main objective for this research is to demonstrate the ITS capabilities in gaining new insight into bubble/turbulence interactions and assisting the development of improved closure laws for multiphase computational fluid dynamics (M-CFD). Both single- and two-phase turbulent flows were studied within a single PWR subchannel. The analysis of numerical results includes the mean gas and liquid velocity profiles, void fraction distribution and turbulent kinetic energy profiles. Two sets of flow rates and bubble sizes were used in the simulations. The chosen flow rates corresponded to the Reynolds numbers of 29,079 and 80,775 based on channel hydraulic diameter (D{sub h}) and mean velocity. The finite element unstructured grids utilized for these simulations include 53.8 million and 1.11 billion elements, respectively. This has allowed to fully resolve all the turbulence scales and the deformable interfaces of individual bubbles. For the two-phase flow simulations, a 1% bubble volume fraction was used which resulted in 17 bubbles in

  4. Taichi-inspired rigid-flexible coupling cellulose-supported solid polymer electrolyte for high-performance lithium batteries

    OpenAIRE

    Zhang, Jianjun; Yue, Liping; Hu, Pu; Liu, Zhihong; Qin, Bingsheng; Zhang, Bo; Wang, Qingfu; DING, GUOLIANG; Zhang, Chuanjian; Zhou, Xinhong; Yao, Jianhua; Cui, Guanglei; Chen, Liquan

    2014-01-01

    Inspired by Taichi, we proposed rigid-flexible coupling concept and herein developed a highly promising solid polymer electrolyte comprised of poly (ethylene oxide), poly (cyano acrylate), lithium bis(oxalate)borate and robust cellulose nonwoven. Our investigation revealed that this new class solid polymer electrolyte possessed comprehensive properties in high mechanical integrity strength, sufficient ionic conductivity (3 × 10−4 S cm−1) at 60°C and improved dimensional thermostability (up to...

  5. Mesoporous carbon spheres with controlled porosity for high-performance lithium-sulfur batteries

    Science.gov (United States)

    Wang, Dexian; Fu, Aiping; Li, Hongliang; Wang, Yiqian; Guo, Peizhi; Liu, Jingquan; Zhao, Xiu Song

    2015-07-01

    Mesoporous carbon (MC) spheres with hierarchical pores, controlled pore volume and high specific surface areas have been prepared by a mass-producible spray drying assisted template method using sodium alginate as carbon precursor and commercial colloidal silica particles as hard template. The resulting MC spheres, possessing hierarchical pores in the range of 3-30 nm, are employed as conductive matrices for the preparation of cathode materials for lithium-sulfur batteries. A high pressure induced one-step impregnation of elemental sulfur into the pore of the MC spheres has been exploited. The electrochemical performances of sulfur-impregnated MC spheres (S-MC) derived from MC spheres with different pore volume and specific surface area but with the same sulfur loading ratio of 60 wt% (S-MC-X-60) have been investigated in details. The S-MC-4-60 composite cathode material displayed a high initial discharge capacity of 1388 mAhg-1 and a good cycling stability of 857 mAhg-1 after 100 cycles at 0.2C, and shows also excellent rate capability of 864 mAhg-1 at 2C. More importantly, the sulfur loading content in MC-4 spheres can reach as high as 80%, and it still can deliver a capacity of 569 mAhg-1 after 100 cycles at 0.2C.

  6. Sulfur/three-dimensional graphene composite for high performance lithium-sulfur batteries

    Science.gov (United States)

    Xu, Chunmei; Wu, Yishan; Zhao, Xuyang; Wang, Xiuli; Du, Gaohui; Zhang, Jun; Tu, Jiangping

    2015-02-01

    A sulfur/graphene composite is prepared by loading elemental sulfur into three-dimensional graphene (3D graphene), which is assembled using a metal ions assisted hydrothermal method. When used as cathode materials for lithium-sulfur (Li-S) batteries, the sulfur/graphene composite (S@3D-graphene) with 73 wt % sulfur shows a significantly enhanced cycling performance (>700 mAh g-1 after 100 cycles at 0.1C rate with a Coulombic efficiency > 96%) as well as high rate capability with a capacity up to 500 mAh g-1 at 2C rate (3.35 A g-1). The superior electrochemical performance could be attributed to the highly porous structure of three-dimensional graphene that not only enables stable and continue pathway for rapid electron and ion transportation, but also restrain soluble polysulfides and suppress the "shuttle effect". Moreover, the robust structure of 3D graphene can keep cathode integrity and accommodate the volume change during high-rate charge/discharge processes, making it a promising candidate as cathode for high performance Li-S batteries.

  7. Sulphur-impregnated flow cathode to enable high-energy-density lithium flow batteries

    Science.gov (United States)

    Chen, Hongning; Zou, Qingli; Liang, Zhuojian; Liu, Hao; Li, Quan; Lu, Yi-Chun

    2015-01-01

    Redox flow batteries are promising technologies for large-scale electricity storage, but have been suffering from low energy density and low volumetric capacity. Here we report a flow cathode that exploits highly concentrated sulphur-impregnated carbon composite, to achieve a catholyte volumetric capacity 294 Ah l-1 with long cycle life (>100 cycles), high columbic efficiency (>90%, 100 cycles) and high energy efficiency (>80%, 100 cycles). The demonstrated catholyte volumetric capacity is five times higher than the all-vanadium flow batteries (60 Ah l-1) and 3-6 times higher than the demonstrated lithium-polysulphide approaches (50-117 Ah l-1). Pseudo-in situ impedance and microscopy characterizations reveal superior electrochemical and morphological reversibility of the sulphur redox reactions. Our approach of exploiting sulphur-impregnated carbon composite in the flow cathode creates effective interfaces between the insulating sulphur and conductive carbon-percolating network and offers a promising direction to develop high-energy-density flow batteries.

  8. Uniform Li2S precipitation on N,O-codoped porous hollow carbon fibers for high-energy-density lithium-sulfur batteries with superior stability.

    Science.gov (United States)

    Qie, Long; Manthiram, Arumugam

    2016-09-21

    A lithium-polysulfide cell with superior stability is reported with N,O-codoped carbon hollow fiber (NCHF) sheets as a current collector. Due to the highly effective chemisorption and physical adsorption of lithium polysulfides on doped NCHF and a uniform Li2S precipitation during cycling, the Li2S6-impregnated NCHF electrodes exhibit high sulfur utilization and superior cycling stability even with a high areal sulfur loading of 6.2 mg cm(-2).

  9. Designing and Thermal Analysis of Safe Lithium Ion Cathode Materials for High Energy Applications

    Science.gov (United States)

    Hu, Enyuan

    Safety is one of the most critical issues facing lithium-ion battery application in vehicles. Addressing this issue requires the integration of several aspects, especially the material chemistry and the battery thermal management. First, thermal stability investigation was carried out on an attractive high energy density material LiNi0.5Mn1.5O4. New findings on the thermal-stability and thermal-decomposition-pathways related to the oxygen-release are discovered for the high-voltage spinel Li xNi0.5Mn1.5O4 (LNMO) with ordered (o-) and disordered (d-) structures at fully delithiated (charged) state using a combination of in situ time-resolved x-ray diffraction (TR-XRD) coupled with mass spectroscopy (MS) and x-ray absorption spectroscopy (XAS). Both fully charged o--LixNi0.5Mn1.5O 4 and d-LixNi0.5Mn1.5O 4 start oxygen-releasing structural changes at temperatures below 300 °C, which is in sharp contrast to the good thermal stability of the 4V-spinel LixMn2O4 with no oxygen being released up to 375 °C. This is mainly caused by the presence of Ni4+ in LNMO, which undergoes dramatic reduction during the thermal decomposition. In addition, charged o-LNMO shows better thermal stability than the d-LNMO counterpart, due to the Ni/Mn ordering and smaller amount of the rock-salt impurity phase in o-LNMO. Newly identified two thermal-decomposition-pathways from the initial LixNi0.5Mn1.5O 4 spinel to the final NiMn2O4-type spinel structure with and without the intermediate phases (NiMnO3 and alpha-Mn 2O3) are found to play key roles in thermal stability and oxygen release of LNMO during thermal decomposition. In addressing the safety issue associated with LNMO, Fe is selected to partially substitute Ni and Mn simultaneously utilizing the electrochemical activity and structure-stabilizing high spin Fe3+. The synthesized LiNi1/3Mn4/3Fe1/3O4 showed superior thermal stability and satisfactory electrochemical performance. At charged state, it is able to withstand the temperature as

  10. Failure modes in high-power lithium-ion batteries for use inhybrid electric vehicles

    Energy Technology Data Exchange (ETDEWEB)

    Kostecki, R.; Zhang, X.; Ross Jr., P.N.; Kong, F.; Sloop, S.; Kerr, J.B.; Striebel, K.; Cairns, E.; McLarnon, F.

    2001-06-22

    The Advanced Technology Development (ATD) Program seeks to aid the development of high-power lithium-ion batteries for hybrid electric vehicles. Nine 18650-size ATD baseline cells were tested under a variety of conditions. The cells consisted of a carbon anode, LiNi{sub 0.8}Co{sub 0.2}O{sub 2} cathode and DEC-EC-LiPF{sub 6} electrolyte, and they were engineered for high-power applications. Selected instrumental techniques such as synchrotron IR microscopy, Raman spectroscopy, scanning electron microscopy, atomic force microscopy, gas chromatography, etc. were used to characterize the anode, cathode, current collectors and electrolyte from these cells. The goal was to identify detrimental processes which lead to battery failure under a high-current cycling regime as well as during storage at elevated temperatures. The diagnostic results suggest that the following factors contribute to the cell power loss: (a) SEI deterioration and non-uniformity on the anode, (b) morphology changes, increase of impedance and phase separation on the cathode, (c) pitting corrosion on the cathode Al current collector, and (d) decomposition of the LiPF{sub 6} salt in the electrolyte at elevated temperature.

  11. Ternary Hybrid Material for High-Performance Lithium-Sulfur Battery.

    Science.gov (United States)

    Fan, Qi; Liu, Wen; Weng, Zhe; Sun, Yueming; Wang, Hailiang

    2015-10-14

    The rechargeable lithium-sulfur battery is a promising option for energy storage applications because of its low cost and high energy density. The electrochemical performance of the sulfur cathode, however, is substantially compromised because of fast capacity decay caused by polysulfide dissolution/shuttling and low specific capacity caused by the poor electrical conductivities of the active materials. Herein we demonstrate a novel strategy to address these two problems by designing and synthesizing a carbon nanotube (CNT)/NiFe2O4-S ternary hybrid material structure. In this unique material architecture, each component synergistically serves a specific purpose: The porous CNT network provides fast electron conduction paths and structural stability. The NiFe2O4 nanosheets afford strong binding sites for trapping polysulfide intermediates. The fine S nanoparticles well-distributed on the CNT/NiFe2O4 scaffold facilitate fast Li(+) storage and release for energy delivery. The hybrid material exhibits balanced high performance with respect to specific capacity, rate capability, and cycling stability with outstandingly high Coulombic efficiency. Reversible specific capacities of 1350 and 900 mAh g(-1) are achieved at rates of 0.1 and 1 C respectively, together with an unprecedented cycling stability of ∼0.009% capacity decay per cycle over more than 500 cycles.

  12. High-loading Fe2O3/SWNT composite films for lithium-ion battery applications

    Science.gov (United States)

    Wang, Ying; Guo, Jiahui; Li, Li; Ge, Yali; Li, Baojun; Zhang, Yingjiu; Shang, Yuanyuan; Cao, Anyuan

    2017-08-01

    Single-walled carbon nanotube (SWNT) films are a potential candidate as porous conductive electrodes for energy conversion and storage; tailoring the loading and distribution of active materials grafted on SWNTs is critical for achieving maximum performance. Here, we show that as-synthesized SWNT samples containing residual Fe catalyst can be directly converted to Fe2O3/SWNT composite films by thermal annealing in air. The mass loading of Fe2O3 nanoparticles is tunable from 63 wt% up to 96 wt%, depending on the annealing temperature (from 450 °C to 600 °C), while maintaining the porous network structure. Interconnected SWNT networks containing high-loading active oxides lead to synergistic effect as an anode material for lithium ion batteries. The performance is improved consistently with increasing Fe2O3 loading. As a result, our Fe2O3/SWNT composite films exhibit a high reversible capacity (1007.1 mA h g-1 at a current density of 200 mA g-1), excellent rate capability (384.9 mA h g-1 at 5 A g-1) and stable cycling performance with the discharge capacity up to 567.1 mA h g-1 after 600 cycles at 2 A g-1. The high-loading Fe2O3/SWNT composite films have potential applications as nanostructured electrodes for various energy devices such as supercapacitors and Li-ion batteries.

  13. High-Temperature Stable Anatase Titanium Oxide Nanofibers for Lithium-Ion Battery Anodes.

    Science.gov (United States)

    Lee, Sangkyu; Eom, Wonsik; Park, Hun; Han, Tae Hee

    2017-08-02

    Control of the crystal structure of electrochemically active materials is an important approach to fabricating high-performance electrodes for lithium-ion batteries (LIBs). Here, we report a methodology for controlling the crystal structure of TiO2 nanofibers by adding aluminum isopropoxide to a common sol-gel precursor solution utilized to create TiO2 nanofibers. The introduction of aluminum cations impedes the phase transformation of electrospun TiO2 nanofibers from the anatase to the rutile phase, which inevitably occurs in the typical annealing process utilized for the formation of TiO2 crystals. As a result, high-temperature stable anatase TiO2 nanofibers were created in which the crystal structure was well-maintained even at high annealing temperatures of up to 700 °C. Finally, the resulting anatase TiO2 nanofibers were utilized to prepare LIB anodes, and their electrochemical performance was compared to pristine TiO2 nanofibers that contain both anatase and rutile phases. Compared to the electrode prepared with pristine TiO2 nanofibers, the electrode prepared with anatase TiO2 nanofibers exhibited excellent electrochemical performances such as an initial Coulombic efficiency of 83.9%, a capacity retention of 89.5% after 100 cycles, and a rate capability of 48.5% at a current density of 10 C (1 C = 200 mA g(-1)).

  14. Unstacked double-layer templated graphene for high-rate lithium-sulphur batteries

    Science.gov (United States)

    Zhao, Meng-Qiang; Zhang, Qiang; Huang, Jia-Qi; Tian, Gui-Li; Nie, Jing-Qi; Peng, Hong-Jie; Wei, Fei

    2014-03-01

    Preventing the stacking of graphene is essential to exploiting its full potential in energy-storage applications. The introduction of spacers into graphene layers always results in a change in the intrinsic properties of graphene and/or induces complexity at the interfaces. Here we show the synthesis of an intrinsically unstacked double-layer templated graphene via template-directed chemical vapour deposition. The as-obtained graphene is composed of two unstacked graphene layers separated by a large amount of mesosized protuberances and can be used for high-power lithium-sulphur batteries with excellent high-rate performance. Even after 1,000 cycles, high reversible capacities of ca. 530 mA h g-1 and 380 mA h g-1 are retained at 5 C and 10 C, respectively. This type of double-layer graphene is expected to be an important platform that will enable the investigation of stabilized three-dimensional topological porous systems and demonstrate the potential of unstacked graphene materials for advanced energy storage, environmental protection, nanocomposite and healthcare applications.

  15. A dual coaxial nanocable sulfur composite for high-rate lithium-sulfur batteries.

    Science.gov (United States)

    Li, Zhen; Yuan, Lixia; Yi, Ziqi; Liu, Yang; Xin, Ying; Zhang, Zhaoliang; Huang, Yunhui

    2014-01-01

    Lithium-sulfur batteries have great potential for some high energy applications such as in electric vehicles and smart grids due to their high capacity, natural abundance, low cost and environmental friendliness. But they suffer from rapid capacity decay and poor rate capability. The problems are mainly related to the dissolution of the intermediate polysulfides in the electrolyte, and to the poor conductivity of sulfur and the discharge products. In this work, we propose a novel dual coaxial nanocable sulfur composite fabricated with multi-walled nanotubes (MWCNT), nitrogen-doped porous carbon (NPC) and polyethylene glycol (PEG), i.e. MWCNTs@S/NPC@PEG nanocable, as a cathode material for Li-S batteries. In such a coaxial structure, the middle N-doped carbon with hierarchical porous structure provides a nanosized capsule to contain and hold the sulfur particles; the inner MWCNTs and the outer PEG layer can further ensure the fast electronic transport and prevent the dissolution of the polysulfides into the electrolyte, respectively. The as-designed MWCNT@S/NPC@PEG composite shows good cycling stability and excellent rate capability. The capacity is retained at 527 mA h g(-1) at 1 C after 100 cycles, and 791 mA h g(-1) at 0.5 C and 551 mA h g(-1) at 2 C after 50 cycles. Especially, the high-rate capability is outstanding with 400 mA h g(-1) at 5 C.

  16. An active core-shell nanoscale design for high voltage cathode of lithium storage devices

    Science.gov (United States)

    Lu, Zhongpei; Liu, Yang; Lu, Xiaojun; Wang, Hao; Yang, Gang; Chao, Yimin; Li, Weili; Yin, Fan

    2017-08-01

    Spinel LiNi0.5Mn1.5O4 (LNM) is a potential high-voltage cathode for commercial lithium-ion batteries (LIBs). Maintaining an appropriate amount of Mn3+ in LNM is necessary to improve the rate performance. However, Mn3+ dissolution in the interface of LNM and electrolyte leads to the fast capacity degradation. Therefore, designing a cathode to prevent Mn3+ loss during charge/discharge is important for high performance LIBs. Here we present an active core-shell design with coating another high-voltage cathode material LiCoPO4 (LCP) on the surface of LNM nanoparticles. The LCP layer can simultaneously induce Mn3+ ions at the interface between LCP and LNM, and act as a stable shell to prevent the loss of Mn3+. The optimized sample LNM@5%LCP possesses 128 mAh g-1 at 0.5 C and 115 mAh g-1 at 20 C rate, and maintains 96% of the initial capacity operated at 55 °C over 100 cycles.

  17. Modeling local chemistry in PWR steam generator crevices

    Energy Technology Data Exchange (ETDEWEB)

    Millett, P.J. [EPRI, Palo Alto, CA (United States)

    1997-02-01

    Over the past two decades steam generator corrosion damage has been a major cost impact to PWR owners. Crevices and occluded regions create thermal-hydraulic conditions where aggressive impurities can become highly concentrated, promoting localized corrosion of the tubing and support structure materials. The type of corrosion varies depending on the local conditions, with stress corrosion cracking being the phenomenon of most current concern. A major goal of the EPRI research in this area has been to develop models of the concentration process and resulting crevice chemistry conditions. These models may then be used to predict crevice chemistry based on knowledge of bulk chemistry, thereby allowing the operator to control corrosion damage. Rigorous deterministic models have not yet been developed; however, empirical approaches have shown promise and are reflected in current versions of the industry-developed secondary water chemistry guidelines.

  18. Non-Flammable, High Voltage Electrolytes for Lithium Ion Batteries Project

    Data.gov (United States)

    National Aeronautics and Space Administration — An electrolyte will be demonstrated for lithium ion batteries with increased range of charge and discharge voltages and with improved fire safety. Experimental...

  19. Novel Anodes for Rapid Recharge High Energy Density Lithium-ion Batteries Project

    Data.gov (United States)

    National Aeronautics and Space Administration — TIAX proposes to develop as a novel negative electrode active material for rechargeable lithium-ion batteries. This material will fill the gap between the...

  20. Valve inlet fluid conditions for pressurizer safety and relief valves in Westinghouse-designed plants. Final report. [PWR

    Energy Technology Data Exchange (ETDEWEB)

    Meliksetian, A.; Sklencar, A.M.

    1982-12-01

    The overpressure transients for Westinghouse-designed NSSSs are reviewed to determine the fluid conditions at the inlet to the PORV and safety valves. The transients considered are: licensing (FSAR) transients; extended operation of high pressure safety injection system; and cold overpressurization. The results of this review, presented in the form of tables and graphs, define the range of fluid conditions expected at the inlet to pressurized safety and power-operated relief valves utilized in Westinghouse-designed PWR units. These results will provide input to the PWR utilities in their justification that the fluid conditions under which their valve designs were tested as part of the EPRI/PWR Safety and Relief Valve Test Program indeed envelop those expected in their units.

  1. Development of high energy pulsed plasma simulator for plasma-lithium trench experiment

    Science.gov (United States)

    Jung, Soonwook

    To simulate detrimental events in a tokamak and provide a test-stand for a liquid lithium infused trench (LiMIT) device, a pulsed plasma source utilizing a theta pinch in conjunction with a coaxial plasma accelerator has been developed. An overall objective of the project is to develop a compact device that can produce 100 MW/m2 to 1 GW/m2 of plasma heat flux (a typical heat flux level in a major fusion device) in ~ 100 mus (≤ 0.1 MJ/m2) for a liquid lithium plasma facing component research. The existing theta pinch device, DEVeX, was built and operated for study on lithium vapor shielding effect. However, a typical plasma energy of 3 - 4 kJ/m2 is too low to study an interaction of plasma and plasma facing components in fusion devices. No or little preionized plasma, ringing of magnetic field, collisions of high energy particles with background gas have been reported as the main issues. Therefore, DEVeX is reconfigured to mitigate these issues. The new device is mainly composed of a plasma gun for a preionization source, a theta pinch for heating, and guiding magnets for a better plasma transportation. Each component will be driven by capacitor banks and controlled by high voltage / current switches. Several diagnostics including triple Langmuir probe, calorimeter, optical emission measurement, Rogowski coil, flux loop, and fast ionization gauge are used to characterize the new device. A coaxial plasma gun is manufactured and installed in the previous theta pinch chamber. The plasma gun is equipped with 500 uF capacitor and a gas puff valve. The increase of the plasma velocity with the plasma gun capacitor voltage is consistent with the theoretical predictions and the velocity is located between the snowplow model and the weak - coupling limit. Plasma energies measured with the calorimeter ranges from 0.02 - 0.065 MJ/m2 and increases with the voltage at the capacitor bank. A cross-check between the plasma energy measured with the calorimeter and the triple probe

  2. Facile Synthesis of V2O5 Hollow Spheres as Advanced Cathodes for High-Performance Lithium-Ion Batteries

    Directory of Open Access Journals (Sweden)

    Xingyuan Zhang

    2017-01-01

    Full Text Available Three-dimensional V2O5 hollow structures have been prepared through a simple synthesis strategy combining solvothermal treatment and a subsequent thermal annealing. The V2O5 materials are composed of microspheres 2–3 μm in diameter and with a distinct hollow interior. The as-synthesized V2O5 hollow microspheres, when evaluated as a cathode material for lithium-ion batteries, can deliver a specific capacity as high as 273 mAh·g−1 at 0.2 C. Benefiting from the hollow structures that afford fast electrolyte transport and volume accommodation, the V2O5 cathode also exhibits a superior rate capability and excellent cycling stability. The good Li-ion storage performance demonstrates the great potential of this unique V2O5 hollow material as a high-performance cathode for lithium-ion batteries.

  3. Facile Synthesis of V₂O₅ Hollow Spheres as Advanced Cathodes for High-Performance Lithium-Ion Batteries.

    Science.gov (United States)

    Zhang, Xingyuan; Wang, Jian-Gan; Liu, Huanyan; Liu, Hongzhen; Wei, Bingqing

    2017-01-18

    Three-dimensional V₂O₅ hollow structures have been prepared through a simple synthesis strategy combining solvothermal treatment and a subsequent thermal annealing. The V₂O₅ materials are composed of microspheres 2-3 μm in diameter and with a distinct hollow interior. The as-synthesized V₂O₅ hollow microspheres, when evaluated as a cathode material for lithium-ion batteries, can deliver a specific capacity as high as 273 mAh·g(-1) at 0.2 C. Benefiting from the hollow structures that afford fast electrolyte transport and volume accommodation, the V₂O₅ cathode also exhibits a superior rate capability and excellent cycling stability. The good Li-ion storage performance demonstrates the great potential of this unique V₂O₅ hollow material as a high-performance cathode for lithium-ion batteries.

  4. Hierarchical nitrogen-doped porous graphene/reduced fluorographene/sulfur hybrids for high-performance lithium-sulfur batteries.

    Science.gov (United States)

    Liu, Zhixuan; Li, Jie; Xiang, Jingwei; Cheng, Shuai; Wu, Hao; Zhang, Na; Yuan, Lixia; Zhang, Wenfeng; Xie, Jia; Huang, Yunhui; Chang, Haixin

    2017-01-18

    It is a great challenge to obtain high performance cathodes with a high sulfur loading and good cycle performance due to the dissolution of intermediate lithium polysulfides in lithium-sulfur batteries. Herein, we report a novel hierarchical hybrid composed of nitrogen-doped porous graphene (NG), reduced fluorographene or graphene fluoride (RFG), and sulfur as a composite cathode in the Li-S batteries. In comparison with sulfur composites based on only either nitrogen-doped porous graphene or pure reduced fluorographene, the hierarchical hybrid of RFG, NG, and sulfur (NG-RFG/S) shows a better reversible capacity and rate capability performance due to a better confinement effect of lithium polysulfides and sulfur. The NG-RFG/S cathode with ∼63.2% S content exhibits a high discharge capacity of 1120 mA h g(-1) and retains 632 mA h g(-1) after 100 cycles at 0.1C. At the higher rate of 0.5C, the cell still maintains a discharge capacity of about 300 mA h g(-1) after 800 cycles, which reveals the great potential of this hybrid cathode for long-cycle-life, high energy density storage applications.

  5. Honeysuckle-derived hierarchical porous nitrogen, sulfur, dual-doped carbon for ultra-high rate lithium ion battery anodes

    Science.gov (United States)

    Ou, Junke; Yang, Lin; Zhang, Zhen; Xi, Xianghui

    2016-11-01

    Nowadays, developing functional carbon materials from cheap natural materials is a highly compelling topic. Different from most explored biomass, honeysuckle is inherently rich in nitrogen and sulfur heteroatoms, and it has many advantages for production on a large scale. Here, hierarchical porous carbon (HPC), derived from waste honeysuckle via an environmentally friendly and economically viable method, has been reported as an anode for rechargeable lithium ion batteries. The as-fabricated HPC exhibits favorable features for electrochemical energy storage performance such as high specific surface area (830 m2 g-1), hierarchical three-dimensional (3D) pore network and heteroatoms (N and S) doping effects. HPC, when evaluated as an anode material for lithium ion batteries, shows superior cycling stability (maintaining a reversible capacity of 1215 mAh g-1 at the current density of 100 mA g-1 after 100 cycles) and excellent rate capability (370 mAh g-1 at the current density of 20 A g-1). Furthermore, owing to the appropriate heteroatoms doping, a high initial coulombic efficiency of 64.7% can be achieved. A widespread comparison with the literature also showed that the honeysuckle derived porous carbon was one of the most promising carbon-based anodes for high-rate lithium ion batteries.

  6. Durable polydopamine-coated porous sulfur core-shell cathode for high performance lithium-sulfur batteries

    Science.gov (United States)

    Deng, Yuanfu; Xu, Hui; Bai, Zhaowen; Huang, Baoling; Su, Jingyang; Chen, Guohua

    2015-12-01

    Lithium-sulfur batteries show fascinating potential for advanced energy system due to their high specific capacity, low-cost, and environmental benignity. However, their wide applications have been plagued by low coulombic efficiency, fast capacity fading and poor rate performance. Herein, a facile method for preparation of S@PDA (PDA = polydopamine) composites with core-shell structure and good electrochemical performance as well as the First-Principles calculations on the interactions of PDA and polysulfides are reported. Taking the advantages of the core-shell structure with porous sulfur core, the high mechanical flexibility of PDA for accommodating the volumetric variation during the discharge/charge processes, the good lithium ion conductivity and the strong chemical interactions between the nitrogen/oxygen atoms with lone electron pair and lithium polysulfides for alleviating their dissolution, the S@PDA composites exhibit high discharge capacities at different current densities (1048 and 869 mAh g-1 at 0.2 and 0.8 A g-1, respectively) and excellent capacity retention capability. A capacity decay as low as 0.021% per cycle and an average coulombic efficiency of 98.5% is observed over a long-term cycling of 890 cycles at 0.8 A g-1. The S@PDA electrode has great potential as a low-cost cathode in high energy Li-S batteries.

  7. Ordered mesoporous carbon/sulfur nanocomposite of high performances as cathode for lithium-sulfur battery

    Energy Technology Data Exchange (ETDEWEB)

    Chen Shuru [State Key Laboratory of Physical Chemistry of Solid Surfaces, Department of Chemistry, College of Chemistry and Chemical Engineering, School of Energy Research, Xiamen University, Xiamen 361005 (China); Zhai Yunpu [Department of Chemistry, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, and Advanced Materials Laboratory, Fudan University, Shanghai 200433 (China); Xu Guiliang; Jiang Yanxia [State Key Laboratory of Physical Chemistry of Solid Surfaces, Department of Chemistry, College of Chemistry and Chemical Engineering, School of Energy Research, Xiamen University, Xiamen 361005 (China); Zhao Dongyuan, E-mail: dyzhao@fudan.edu.cn [Department of Chemistry, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, and Advanced Materials Laboratory, Fudan University, Shanghai 200433 (China); Li Juntao; Huang Ling [State Key Laboratory of Physical Chemistry of Solid Surfaces, Department of Chemistry, College of Chemistry and Chemical Engineering, School of Energy Research, Xiamen University, Xiamen 361005 (China); Sun Shigang, E-mail: sgsun@xmu.edu.cn [State Key Laboratory of Physical Chemistry of Solid Surfaces, Department of Chemistry, College of Chemistry and Chemical Engineering, School of Energy Research, Xiamen University, Xiamen 361005 (China)

    2011-11-01

    Ordered mesoporous carbon/sulfur (OMC/S) nanocomposites with hierarchically structured sulfur loading, ranging from 50 to 75 wt%, were synthesized via a simple melt-diffusion strategy. The OMC with a BET surface area of 2102 m{sup 2} g{sup -1}, a pore volume of 2.0 cm{sup 3} g{sup -1} and unique bimodal mesoporous (5.6/2.3 nm) structure, was prepared from a triconstituent co-assembly method. The resulting OMC/S nanocomposite material served as cathode of rechargeable lithium-sulfur (Li-S) battery. It has been tested that the novel OMC/S cathode can deliver a superior reversible capacity and cyclability. In particular, the nanocomposite with a loading of 60 wt% sulfur (OMC/S-60) presents the highest sulfur utilization ca. 70%, an excellent high rate capability ca. 6 C and a good cycling stability for up to 400 full charge-discharge cycles. The exceptional electrochemical performances are exclusively attributed to the large internal surface area and high porosity of the ordered mesoporous carbon, which favorites both electron and Li-ion transportations.

  8. Theoretical evaluation of high-energy lithium metal phosphate cathode materials in Li-ion batteries

    Science.gov (United States)

    Howard, Wilmont F.; Spotnitz, Robert M.

    Lithium metal phosphates (olivines) are emerging as long-lived, safe cathode materials in Li-ion batteries. Nano-LiFePO 4 already appears in high-power applications, and LiMnPO 4 development is underway. Current and emerging Fe- and Mn-based intercalants, however, are low-energy producers compared to Ni and Co compounds. LiNiPO 4, a high voltage olivine, has the potential for superior energy output (>10.7 Wh in 18650 batteries), compared with commercial Li(Co,Ni)O 2 derivatives (up to 9.9 Wh). Speculative Co and Ni olivine cathode materials charged to above 4.5 V will require significant advances in electrolyte compositions and nanotechnology before commercialization. The major drivers toward 5 V battery chemistries are the inherent abuse tolerance of phosphates and the economic benefit of LiNiPO 4: it can produce 34% greater energy per dollar of cell material cost than LiAl 0.05Co 0.15Ni 0.8O 2, today's "standard" cathode intercalant in Li-ion batteries.

  9. Biomimetic Ant-Nest Electrode Structures for High Sulfur Ratio Lithium-Sulfur Batteries.

    Science.gov (United States)

    Ai, Guo; Dai, Yiling; Mao, Wenfeng; Zhao, Hui; Fu, Yanbao; Song, Xiangyun; En, Yunfei; Battaglia, Vincent S; Srinivasan, Venkat; Liu, Gao

    2016-09-14

    The lithium-sulfur (Li-S) rechargeable battery has the benefit of high gravimetric energy density and low cost. Significant research currently focuses on increasing the sulfur loading and sulfur/inactive-materials ratio, to improve life and capacity. Inspired by nature's ant-nest structure, this research results in a novel Li-S electrode that is designed to meet both goals. With only three simple manufacturing-friendly steps, which include slurry ball-milling, doctor-blade-based laminate casting, and the use of the sacrificial method with water to dissolve away table salt, the ant-nest design has been successfully recreated in an Li-S electrode. The efficient capabilities of the ant-nest structure are adopted to facilitate fast ion transportation, sustain polysulfide dissolution, and assist efficient precipitation. High cycling stability in the Li-S batteries, for practical applications, has been achieved with up to 3 mg·cm(-2) sulfur loading. Li-S electrodes with up to a 85% sulfur ratio have also been achieved for the efficient design of this novel ant-nest structure.

  10. A Praline-Like Flexible Interlayer with Highly Mounted Polysulfide Anchors for Lithium-Sulfur Batteries.

    Science.gov (United States)

    Zhao, Teng; Ye, Yusheng; Lao, Cheng-Yen; Divitini, Giorgio; Coxon, Paul R; Peng, Xiaoyu; He, Xiong; Kim, Hyun-Kyung; Xi, Kai; Ducati, Caterina; Chen, Renjie; Liu, Yingjun; Ramakrishna, Seeram; Kumar, Ramachandran Vasant

    2017-08-21

    The development of lithium-sulfur (Li-S) batteries is dogged by the rapid capacity decay arising from polysulfide dissolution and diffusion in organic electrolytes. To solve this critical issue, a praline-like flexible interlayer consisting of high-loading titanium oxide (TiO2 ) nanoparticles and relatively long carbon nanofibers is fabricated. TiO2 nanoparticles with a size gradient occupy both the external and internal of carbon fiber and serve as anchors that allow the chemical adsorption of polysulfides through a conductive nanoarchitecture. The porous conductive carbon backbone helps in the physical absorption of polysulfides and provides redox reaction sites to allow the polysulfides to be reused. More importantly, it offers enough mechanical strength to support a high load TiO2 nanoparticle (79 wt%) that maximizes their chemical role, and can accommodate the large volume changes. Significant enhancement in cycle stability and rate capability is achieved for a readily available sulfur/multi-walled carbon nanotube composite cathode simply by incorporating this hierarchically nanostructured interlayer. The design and synthesis of interlayers by in situ integration of metal oxides and carbon fibers via a simple route offers the potential to advance Li-S batteries for practical applications in the future. © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  11. Electrochemically Formed Ultrafine Metal Oxide Nanocatalysts for High-Performance Lithium-Oxygen Batteries.

    Science.gov (United States)

    Liu, Bin; Yan, Pengfei; Xu, Wu; Zheng, Jianming; He, Yang; Luo, Langli; Bowden, Mark E; Wang, Chong-Min; Zhang, Ji-Guang

    2016-08-10

    Lithium-oxygen (Li-O2) batteries have an extremely high theoretical specific energy density when compared with conventional energy-storage systems. However, practical application of the Li-O2 battery system still faces significant challenges. In this work, we report a new approach for synthesis of ultrafine metal oxide nanocatalysts through an electrochemical prelithiation process. This process reduces the size of NiCo2O4 (NCO) particles from 20-30 nm to a uniformly distributed domain of ∼2 nm and significantly improves their catalytic activity. Structurally, the prelithiated NCO nanowires feature ultrafine NiO/CoO nanoparticles that are highly stable during prolonged cycles in terms of morphology and particle size, thus maintaining an excellent catalytic effect to oxygen reduction and evolution reactions. A Li-O2 battery using this catalyst demonstrated an initial capacity of 29 280 mAh g(-1) and retained a capacity of >1000 mAh g(-1) after 100 cycles based on the weight of the NCO active material. Direct in situ transmission electron microscopy observations conclusively revealed the lithiation/delithiation process of as-prepared NCO nanowires and provided in-depth understanding for both catalyst and battery chemistries of transition-metal oxides. This unique electrochemical approach could also be used to form ultrafine nanoparticles of a broad range of materials for catalyst and other applications.

  12. A Highly Active Low Voltage Redox Mediator for Enhanced Rechargeability of Lithium-Oxygen Batteries.

    Science.gov (United States)

    Kundu, Dipan; Black, Robert; Adams, Brian; Nazar, Linda F

    2015-12-23

    Owing to its high theoretical specific energy, the Li-oxygen battery is one of the fundamentally most promising energy storage systems, but also one of the most challenging. Poor rechargeability, involving the oxidation of insoluble and insulating lithium peroxide (Li2O2), has remained the "Achilles' heel" of this electrochemical energy storage system. We report here on a new redox mediator tris[4-(diethylamino)phenyl]amine (TDPA), that-at 3.1 V-exhibits the lowest and closest potential redox couple compared to the equilibrium voltage of the Li-oxygen cell of those reported to date, with a second couple also at a low potential of 3.5 V. We show it is a soluble "catalyst" capable of lowering the Li2O2 charging potential by >0.8 V without requiring direct electrical contact of the peroxide and that it also facilitates high discharge capacities. Its chemical and electrochemical stability, fast diffusion kinetics, and two dynamic redox potentials represent a significant advance in oxygen-evolution catalysis. It enables Li-O2 cells that can be recharged more than 100 cycles with average round-trip efficiencies >80%, opening a new avenue for practical Li-oxygen batteries.

  13. Sulfur nanocrystals anchored graphene composite with highly improved electrochemical performance for lithium-sulfur batteries

    Science.gov (United States)

    Zhang, Jun; Dong, Zimin; Wang, Xiuli; Zhao, Xuyang; Tu, Jiangping; Su, Qingmei; Du, Gaohui

    2014-12-01

    Two kinds of graphene-sulfur composites with 50 wt% of sulfur are prepared using hydrothermal method and thermal mixing, respectively. Transmission Electron Microscopy (TEM) and Energy Dispersive X-ray Spectra mapping show that sulfur nanocrystals with size of ∼5 nm dispersed on graphene sheets homogeneously for the sample prepared by hydrothermal method (NanoS@G). While for the thermal mixed graphene-sulfur composite (S-G mixture), sulfur shows larger and uneven size (50-200 nm). X-ray Photoelectron Spectra (XPS) reveals the strong chemical bonding between the sulfur nanocrystals and graphene. Comparing with the S-G mixture, the NanoS@G composite shows highly improved electrochemical performance as cathode for lithium-sulfur (Li-S) battery. The NanoS@G composite delivers an initial capacity of 1400 mAh g-1 with the sulfur utilization of 83.7% at a current density of 335 mA g-1. The capacity keeps above 720 mAh g-1 over 100 cycles. The strong adherence of the sulfur nanocrystals on graphene immobilizes sulfur and polysulfides species and suppressed the "shuttle effect", resulting higher coulombic efficiency and better capacity retention. Electrochemical impedance also suggests that the strong bonding enabled rapid electronic/ionic transport and improved electrochemical kinetics, therefore good rate capability is obtained. These results demonstrate that the NanoS@G composite is a very promising candidate for high-performance Li-S batteries.

  14. High-capacity, low-tortuosity, and channel-guided lithium metal anode

    Science.gov (United States)

    Zhang, Ying; Luo, Wei; Wang, Chengwei; Li, Yiju; Chen, Chaoji; Song, Jianwei; Dai, Jiaqi; Hitz, Emily M.; Xu, Shaomao; Yang, Chunpeng; Wang, Yanbin; Hu, Liangbing

    2017-04-01

    Lithium metal anode with the highest capacity and lowest anode potential is extremely attractive to battery technologies, but infinite volume change during the Li stripping/plating process results in cracks and fractures of the solid electrolyte interphase, low Coulombic efficiency, and dendritic growth of Li. Here, we use a carbonized wood (C-wood) as a 3D, highly porous (73% porosity) conductive framework with well-aligned channels as Li host material. We discovered that molten Li metal can infuse into the straight channels of C-wood to form a Li/C-wood electrode after surface treatment. The C-wood channels function as excellent guides in which the Li stripping/plating process can take place and effectively confine the volume change that occurs. Moreover, the local current density can be minimized due to the 3D C-wood framework. Therefore, in symmetric cells, the as-prepared Li/C-wood electrode presents a lower overpotential (90 mV at 3 mAṡcm-2), more-stable stripping/plating profiles, and better cycling performance (˜150 h at 3 mAṡcm-2) compared with bare Li metal electrode. Our findings may open up a solution for fabricating stable Li metal anode, which further facilitates future application of high-energy-density Li metal batteries.

  15. Copper-Doped Titanium Dioxide Bronze Nanowires with Superior High Rate Capability for Lithium Ion Batteries.

    Science.gov (United States)

    Zhang, Yongquan; Meng, Yuan; Zhu, Kai; Qiu, Hailong; Ju, Yanming; Gao, Yu; Du, Fei; Zou, Bo; Chen, Gang; Wei, Yingjin

    2016-03-01

    Pristine and Cu-doped TiO2-B nanowires are synthesized by the microwave assisted hydrothermal method. The doped oxide exhibits a highly porous structure with a specific surface area of 160.7 m(2) g(-1). As evidenced by X-ray photoelectron spectroscopy and X-ray energy dispersive spectroscopy, around 2.0 atom % Cu(2+) cations are introduced into TiO2-B, which leads to not only a slightly expanded lattice network but also, more importantly, a modified electronic structure. The band gap of TiO2-B is reduced from 2.94 to 2.55 eV, resulting in enhanced electronic conductivity. Cyclic voltammetry and electrochemical impedance spectroscopy reveal improved electrochemical kinetic properties of TiO2-B due to the Cu doping. The doped nanowires show a specific capacity of 186.8 mAh g(-1) at the 10 C rate with a capacity retention of 64.3% after 2000 cycles. Remarkably, our material exhibits a specific capacity of 150 mAh g(-1) at the 60 C rate, substantiating its superior high rate capability for rechargeable lithium batteries.

  16. Hollow Porous VOx/C Nanoscrolls as High-Performance Anodes for Lithium-Ion Batteries.

    Science.gov (United States)

    Jia, Bao-Rui; Qin, Ming-Li; Zhang, Zi-Li; Li, Shu-Mei; Zhang, De-Yin; Wu, Hao-Yang; Zhang, Lin; Lu, Xin; Qu, Xuan-Hui

    2016-10-05

    Novel hollow porous VOx/C nanoscrolls are synthesized by an annealing process with the VOx/octadecylamine (ODA) nanoscrolls as both vanadium and carbon sources. In the preparation, the VOx/ODA nanoscrolls are first achieved by a two-phase solvothermal method using ammonium metavanadat as the precursor. Upon subsequent heating, the intercalated amines between the vanadate layers in the VOx/ODA nanoscrolls decompose into gases, which escape from inside the nanoscrolls and leave sufficient pores in the walls. As the anodes of lithium-ion batteries (LIBs), such hollow porous VOx/C nanoscrolls possess exceedingly high capacity and rate capability (904 mAh g(-1) at 1 A g(-1)) and long cyclic stability (872 mAh g(-1) after 210 cycles at 1 A g(-1)). The good performance is derived from the unique structural features of the hollow hierarchical porous nanoscrolls with low crystallinity, which could significantly suppress irreversible Li(+) trapping as well as improve Li(+) diffusion kinetics. This universal method of annealing amine-intercalated oxide could be widely applied to the fabrication of a variety of porous electrode materials for high-performance LIBs and supercapacitors.

  17. Cobalt Oxide Porous Nanofibers Directly Grown on Conductive Substrate as a Binder/Additive-Free Lithium-Ion Battery Anode with High Capacity.

    Science.gov (United States)

    Liu, Hao; Zheng, Zheng; Chen, Bochao; Liao, Libing; Wang, Xina

    2017-12-01

    In order to reduce the amount of inactive materials, such as binders and carbon additives in battery electrode, porous cobalt monoxide nanofibers were directly grown on conductive substrate as a binder/additive-free lithium-ion battery anode. This electrode exhibited very high specific discharging/charging capacities at various rates and good cycling stability. It was promising as high capacity anode materials for lithium-ion battery.

  18. Horizontal Drop of 21- PWR Waste Package

    Energy Technology Data Exchange (ETDEWEB)

    A.K. Scheider

    2001-04-26

    The objective of this calculation is to determine the structural response of the waste package (WP) dropped horizontally from a specified height. The WP used for that purpose is the 21-Pressurized Water Reactor (PWR) WP. The scope of this document is limited to reporting the calculation results in terms of stress intensities. The information provided by the sketches (Attachment I) is that of the potential design of the type of WP considered in this calculation, and all obtained results are valid for that design only. This calculation is associated with the WP design and was performed by the Waste Package Design group in accordance with the ''Technical Work Plan for: Waste Package Design Description for LA'' (Ref. 16). AP-3.12Q, ''Calculations'' (Ref. 11) is used to perform the calculation and develop the document. The sketches attached to this calculation provide the potential dimensions and materials for the 21-PWR WP design.

  19. Thermo-Mechanical Analyses of the High Heat Flux Component for ITER Dual Functional Lithium Lead Test Blanket Module

    Institute of Scientific and Technical Information of China (English)

    CHEN Hongli; BAI Yunqing

    2009-01-01

    The finite element code ANSYS is used to calculate the temperature and stress distributions for the first wall of DFLL-TBM (dual functional lithium lead-test blanket module),for testing in ITER. Preliminary analyses indicate that not only the low temperature design rules,the well-known 3Sm rules, are satisfied for the first wall, but the additional high temperature structural design criteria for the creep damage limits and creep-ratcheting limits are met as well.

  20. A model Based Desing of a Thermal Management System for a High Power Lithium-Ion Battery Pack.

    OpenAIRE

    Nieto Aguirrezabala, N. (Nerea); Blanco Barro, F.J. (Francisco Javier); Ramos, J.C. (Juan Carlos)

    2014-01-01

    In the present thesis an improved design methodology is proposed for TMSs (Thermal Management Systems) for high power lithium-ion battery packs used in traction applications. The methodology involves the development of different mathematical models for heat generation, transmission, and dissipation and their coupling and integration in the battery pack design methodology in order to improve overall safety and performance. The sequence of steps to be followed according to the...

  1. High-Capacity Micrometer-Sized Li 2 S Particles as Cathode Materials for Advanced Rechargeable Lithium-Ion Batteries

    KAUST Repository

    Yang, Yuan

    2012-09-19

    Li 2S is a high-capacity cathode material for lithium metal-free rechargeable batteries. It has a theoretical capacity of 1166 mAh/g, which is nearly 1 order of magnitude higher than traditional metal oxides/phosphates cathodes. However, Li 2S is usually considered to be electrochemically inactive due to its high electronic resistivity and low lithium-ion diffusivity. In this paper, we discover that a large potential barrier (∼1 V) exists at the beginning of charging for Li 2S. By applying a higher voltage cutoff, this barrier can be overcome and Li 2S becomes active. Moreover, this barrier does not appear again in the following cycling. Subsequent cycling shows that the material behaves similar to common sulfur cathodes with high energy efficiency. The initial discharge capacity is greater than 800 mAh/g for even 10 μm Li 2S particles. Moreover, after 10 cycles, the capacity is stabilized around 500-550 mAh/g with a capacity decay rate of only ∼0.25% per cycle. The origin of the initial barrier is found to be the phase nucleation of polysulfides, but the amplitude of barrier is mainly due to two factors: (a) charge transfer directly between Li 2S and electrolyte without polysulfide and (b) lithium-ion diffusion in Li 2S. These results demonstrate a simple and scalable approach to utilizing Li 2S as the cathode material for rechargeable lithium-ion batteries with high specific energy. © 2012 American Chemical Society.

  2. The Role of Lithium Conditioning in Achieving High Performance, Long Pulse H-mode Discharges in the NSTX and EAST Devices

    Energy Technology Data Exchange (ETDEWEB)

    Maingi, Rajesh [PPPL; Mansfield, D. K. [PPPL; Gong, X. Z. [IPPCAS; Sun, Z. [IPPCAS; Bell, M. G. [PPPL

    2014-10-01

    In this paper, the role of lithium wall conditioning on the achievement of high performance, long pulse discharges in the National Spherical Torus Experiment (NSTX) and the Experimental Advanced Superconducting Tokamak (EAST) is documented. Common observations include recycling reduction and elimination of ELMs. In NSTX, lithium conditioning typically resulted in ELM-free operation with impurity accumulation, which was ameliorated e.g. with pulsed 3D fields to trigger controlled ELMs. Active lithium conditioning in EAST discharges has overcome this problem, producing an ELM-free Hmode with controlled density and impurities.

  3. Highly-flexible 3D Li2S/graphene cathode for high-performance lithium sulfur batteries

    Science.gov (United States)

    He, Jiarui; Chen, Yuanfu; Lv, Weiqiang; Wen, Kechun; Li, Pingjian; Qi, Fei; Wang, Zegao; Zhang, Wanli; Li, Yanrong; Qin, Wu; He, Weidong

    2016-09-01

    Three-dimensional Li2S/graphene hierarchical architecture (3DLG) is synthesized with a facile infiltration method. Highly-crystalline Li2S nanoparticles are deposited homogenously into three-dimensional graphene foam (3DGF) network grown by chemical vapor deposition (CVD), resulting in 3DLG with high surface area, porosity, flexibility and conductivity. The 3DLG is employed as flexible, free-standing and binder-free cathode without metallic current collectors or conducting additives. Due to the unique structure, the 3DLG exhibits a high discharge capacity of 894.7 mAh g-1 at 0.1 C, a high capacity retention of 87.7% after 300 cycles at 0.2 C, and the high-rate capacity up to 4 C reaches 598.6 mAh g-1. The cyclic performance is record-breaking compared to the previous reports on free-standing graphene-Li2S cathodes. Flexible lithium-sulfur batteries based on the high-capacity 3DLG cathode have promising application potentials in flexible electronics, electrical vehicles, etc.

  4. Identifying thermal cycling mechanisms in PWR branch line piping

    Energy Technology Data Exchange (ETDEWEB)

    Rosinski, S.T. [EPRI, Charlotte, NC (United States); Keller, J.D.; Bilanin, A.J. [Continuum Dynamics, Inc., Ewing, NJ (United States)

    2002-07-01

    Predicting the onset and the characteristics of thermal cycling in pressurized water reactor (PWR) branch line piping systems is critical to formulation of thermal fatigue screening tools. The complex nature of the underlying thermal-hydraulic phenomena, however, significantly complicates prediction using analytical models or direct numerical simulations. Instead, it is necessary to perform scaled experiments to identify the physical mechanisms and to gather data for formulation of semi-empirical models for the thermal cycling phenomena. Through the EPRI Materials Reliability Program a test program is underway to identify and develop semi-empirical correlations for the physical thermalhydraulic mechanisms that cause thermal cycling in dead-ended PWR branch line piping systems. Three series of tests are being performed in this test program: configuration tests on a representative up-horizontal (UH) branch line piping geometry, configuration tests on a representative down-horizontal (DH) branch line piping geometry, and high Reynolds number tests to assess penetration of secondary flow structures into a dead-ended branch line. Results from UH and DH configuration tests indicate that random turbulence penetration is not sufficient for thermal cycling to occur. Rather a swirling flow structure, representative of a large, 'corkscrew' vortical structure, is required for thermal cycling. Scale tests on the UH configuration have simulated cycling phenomena observed in full-scale plant data and have been used to determine parametric sensitivities in formulating a predictive model for the thermal cycling. Data indicate that the mechanism for thermal cycling in UH configurations is stochastic but scales with the leak rate from the valve. The critical dependent variables are reduced to several non-dimensional scaling curves, resulting in a semiempirical predictive model. This paper discusses the test program and the results obtained to date. Application of these

  5. Octahedral Tin Dioxide Nanocrystals Anchored on Vertically Aligned Carbon Aerogels as High Capacity Anode Materials for Lithium-Ion Batteries

    Science.gov (United States)

    Liu, Mingkai; Liu, Yuqing; Zhang, Yuting; Li, Yiliao; Zhang, Peng; Yan, Yan; Liu, Tianxi

    2016-08-01

    A novel binder-free graphene - carbon nanotubes - SnO2 (GCNT-SnO2) aerogel with vertically aligned pores was prepared via a simple and efficient directional freezing method. SnO2 octahedrons exposed of {221} high energy facets were uniformly distributed and tightly anchored on multidimensional graphene/carbon nanotube (GCNT) composites. Vertically aligned pores can effectively prevent the emersion of “closed” pores which cannot load the active SnO2 nanoparticles, further ensure quick immersion of electrolyte throughout the aerogel, and can largely shorten the transport distance between lithium ions and active sites of SnO2. Especially, excellent electrical conductivity of GCNT-SnO2 aerogel was achieved as a result of good interconnected networks of graphene and CNTs. Furthermore, meso- and macroporous structures with large surface area created by the vertically aligned pores can provide great benefit to the favorable transport kinetics for both lithium ion and electrons and afford sufficient space for volume expansion of SnO2. Due to the well-designed architecture of GCNT-SnO2 aerogel, a high specific capacity of 1190 mAh/g with good long-term cycling stability up to 1000 times was achieved. This work provides a promising strategy for preparing free-standing and binder-free active electrode materials with high performance for lithium ion batteries and other energy storage devices.

  6. High Rate, Long Lifespan LiV3 O8 Nanorods as a Cathode Material for Lithium-Ion Batteries.

    Science.gov (United States)

    Chen, Zhongxue; Xu, Fei; Cao, Shunan; Li, Zhengfeng; Yang, Hanxi; Ai, Xinping; Cao, Yuliang

    2017-05-01

    LiV3 O8 nanorods with controlled size are successfully synthesized using a nonionic triblock surfactant Pluronic-F127 as the structure directing agent. X-ray diffraction, scanning electron microscopy, and transmission electron microscopy techniques are used to characterize the samples. It is observed that the nanorods with a length of 4-8 µm and diameter of 0.5-1.0 µm distribute uniformly. The resultant LiV3 O8 nanorods show much better performance as cathode materials in lithium-ion batteries than normal LiV3 O8 nanoparticles, which is associated with the their unique micro-nano-like structure that can not only facilitate fast lithium ion transport, but also withstand erosion from electrolytes. The high discharge capacity (292.0 mAh g(-1) at 100 mA g(-1) ), high rate capability (138.4 mAh g(-1) at 6.4 A g(-1) ), and long lifespan (capacity retention of 80.5% after 500 cycles) suggest the potential use of LiV3 O8 nanorods as alternative cathode materials for high-power and long-life lithium ion batteries. In particular, the synthetic strategy may open new routes toward the facile fabrication of nanostructured vanadium-based compounds for energy storage applications. © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  7. Modification of SnO2 Anodes by Atomic Layer Deposition for High Performance Lithium Ion Batteries

    KAUST Repository

    Yesibolati, Nulati

    2013-05-01

    Tin dioxide (SnO2) is considered one of the most promising anode materials for Lithium ion batteries (LIBs), due to its large theoretical capacity and natural abundance. However, its low electronic/ionic conductivities, large volume change during lithiation/delithiation and agglomeration prevent it from further commercial applications. In this thesis, we investigate modified SnO2 as a high energy density anode material for LIBs. Specifically two approaches are presented to improve battery performances. Firstly, SnO2 electrochemical performances were improved by surface modification using Atomic Layer Deposition (ALD). Ultrathin Al2O3 or HfO2 were coated on SnO2 electrodes. It was found that electrochemical performances had been enhanced after ALD deposition. In a second approach, we implemented a layer-by-layer (LBL) assembled graphene/carbon-coated hollow SnO2 spheres as anode material for LIBs. Our results indicated that the LBL assembled electrodes had high reversible lithium storage capacities even at high current densities. These superior electrochemical performances are attributed to the enhanced electronic conductivity and effective lithium diffusion, because of the interconnected graphene/carbon networks among nanoparticles of the hollow SnO2 spheres.

  8. Octahedral Tin Dioxide Nanocrystals Anchored on Vertically Aligned Carbon Aerogels as High Capacity Anode Materials for Lithium-Ion Batteries

    Science.gov (United States)

    Liu, Mingkai; Liu, Yuqing; Zhang, Yuting; Li, Yiliao; Zhang, Peng; Yan, Yan; Liu, Tianxi

    2016-01-01

    A novel binder-free graphene - carbon nanotubes - SnO2 (GCNT-SnO2) aerogel with vertically aligned pores was prepared via a simple and efficient directional freezing method. SnO2 octahedrons exposed of {221} high energy facets were uniformly distributed and tightly anchored on multidimensional graphene/carbon nanotube (GCNT) composites. Vertically aligned pores can effectively prevent the emersion of “closed” pores which cannot load the active SnO2 nanoparticles, further ensure quick immersion of electrolyte throughout the aerogel, and can largely shorten the transport distance between lithium ions and active sites of SnO2. Especially, excellent electrical conductivity of GCNT-SnO2 aerogel was achieved as a result of good interconnected networks of graphene and CNTs. Furthermore, meso- and macroporous structures with large surface area created by the vertically aligned pores can provide great benefit to the favorable transport kinetics for both lithium ion and electrons and afford sufficient space for volume expansion of SnO2. Due to the well-designed architecture of GCNT-SnO2 aerogel, a high specific capacity of 1190 mAh/g with good long-term cycling stability up to 1000 times was achieved. This work provides a promising strategy for preparing free-standing and binder-free active electrode materials with high performance for lithium ion batteries and other energy storage devices. PMID:27510357

  9. Dynamic behaviour of interphases and its implication on high-energy-density cathode materials in lithium-ion batteries

    Science.gov (United States)

    Li, Wangda; Dolocan, Andrei; Oh, Pilgun; Celio, Hugo; Park, Suhyeon; Cho, Jaephil; Manthiram, Arumugam

    2017-01-01

    Undesired electrode–electrolyte interactions prevent the use of many high-energy-density cathode materials in practical lithium-ion batteries. Efforts to address their limited service life have predominantly focused on the active electrode materials and electrolytes. Here an advanced three-dimensional chemical and imaging analysis on a model material, the nickel-rich layered lithium transition-metal oxide, reveals the dynamic behaviour of cathode interphases driven by conductive carbon additives (carbon black) in a common nonaqueous electrolyte. Region-of-interest sensitive secondary-ion mass spectrometry shows that a cathode-electrolyte interphase, initially formed on carbon black with no electrochemical bias applied, readily passivates the cathode particles through mutual exchange of surface species. By tuning the interphase thickness, we demonstrate its robustness in suppressing the deterioration of the electrode/electrolyte interface during high-voltage cell operation. Our results provide insights on the formation and evolution of cathode interphases, facilitating development of in situ surface protection on high-energy-density cathode materials in lithium-based batteries. PMID:28443608

  10. Multifunctional Nitrogen-Doped Loofah Sponge Carbon Blocking Layer for High-Performance Rechargeable Lithium Batteries.

    Science.gov (United States)

    Gu, Xingxing; Tong, Chuan-Jia; Rehman, Sarish; Liu, Li-Min; Hou, Yanglong; Zhang, Shanqing

    2016-06-29

    Low-cost, long-life, and high-performance lithium batteries not only provide an economically viable power source to electric vehicles and smart electricity grids but also address the issues of the energy shortage and environmental sustainability. Herein, low-cost, hierarchically porous, and nitrogen-doped loofah sponge carbon (N-LSC) derived from the loofah sponge has been synthesized via a simple calcining process and then applied as a multifunctional blocking layer for Li-S, Li-Se, and Li-I2 batteries. As a result of the ultrahigh specific area (2551.06 m(2) g(-1)), high porosity (1.75 cm(3) g(-1)), high conductivity (1170 S m(-1)), and heteroatoms doping of N-LSC, the resultant Li-S, Li-Se, and Li-I2 batteries with the N-LSC-900 membrane deliver outstanding electrochemical performance stability in all cases, i.e., high reversible capacities of 623.6 mA h g(-1) at 1675 mA g(-1) after 500 cycles, 350 mA h g(-1) at 1356 mA g(-1) after 1000 cycles, and 150 mA h g(-1) at 10550 mA g(-1) after 5000 cycles, respectively. The successful application to Li-S, Li-Se, and Li-I2 batteries suggests that loofa sponge carbon could play a vital role in modern rechargeable battery industries as a universal, cost-effective, environmentally friendly, and high-performance blocking layer.

  11. Study of safety relief valve operation under ATWS conditions. [PWR

    Energy Technology Data Exchange (ETDEWEB)

    Hutmacher, E.S.; Nesmith, B.J.; Brukiewa, J.B.

    1979-06-25

    A literature survey and analysis project has been performed to determine if recent (since mid-1975) data has been reported which could influence the current approach to predicting PWR relief valve capacity under ATWS conditions. This study was conducted by the Energy Technology Engineering Center for NRC. Results indicate that the current relief valve capacity model tends to predict less capacity than actually obtains; however, no experimental verification at PWR ATWS conditions was found. Other project objectives were to establish the availability of methods for evaluating reaction forces and back pressure effects on relief valve capacity, and to determine if facilities exist which are capable of testing PWR relief valves at ATWS conditions.

  12. TiS2-MWCNT hybrid as high performance anode in lithium-ion battery

    Science.gov (United States)

    Kartick, B.; Srivastava, Suneel Kumar; Mahanty, Sourindra

    2013-09-01

    The present work reports the preparation of hybrids by simple dry grinding of titanium sulfide (TiS2) and multi-walled carbon nanotubes (MWCNTs) in different weight ratio and their characterization. X-ray diffraction and Raman studies indicated the presence of interaction between the TiS2 and MWCNT. Field emission scanning electron microscopy and high resolution transmission electron microscopy showed the formation of three-dimensional architecture and co-dispersion in TiS2-MWCNT (1:1) hybrid. X-ray photoelectron spectroscopy also confirmed the presence of TiS2 and MWCNT in the prepared hybrid. Thermogravimetric analysis indicated an increase in thermal stability with higher MWCNT content. The results of the electrochemical analyses indicated that TiS2-MWCNT (1:1) hybrid exhibited an enhanced performance as lithium-ion battery anode. The initial specific capacity was found to be ≈450 mAh g-1 with 80 % retention in capacity after 50 discharge-charge cycles. These values are significantly higher compared to those for TiS2, MWCNT or other TiS2-MWCNT hybrids. Such improved performance is attributed to the presence of a synergistic effect between TiS2 and MWCNT.

  13. Graphene-based lithium ion capacitor with high gravimetric energy and power densities

    Science.gov (United States)

    Ajuria, Jon; Arnaiz, Maria; Botas, Cristina; Carriazo, Daniel; Mysyk, Roman; Rojo, Teofilo; Talyzin, Alexandr V.; Goikolea, Eider

    2017-09-01

    Hybrid capacitor configurations are now of increasing interest to overcome the current energy limitations of supercapacitors. In this work, we report a lithium ion capacitor (LIC) entirely based on graphene. On the one hand, the negative -battery-type- electrode consists of a self-standing, binder-free 3D macroporous foam formed by reduced graphene oxide and decorated with tin oxide nanoparticles (SnO2-rGO). On the other hand, the positive -capacitor-type- electrode is based on a thermally expanded and physically activated reduced graphene oxide (a-TEGO). For comparison purposes, a symmetric electrical double layer capacitor (EDLC) using the same activated graphene in 1.5 M Et4NBF4/ACN electrolyte is also assembled. Built in 1 M LiPF6 EC:DMC, the graphene-based LIC shows an outstanding, 10-fold increase in energy density with respect to its EDLC counterpart at low discharge rates (up to 200 Wh kg-1). Furthermore, it is still capable to deliver double the energy in the high power region, within a discharge time of few seconds.

  14. Novel germanium/polypyrrole composite for high power lithium-ion batteries.

    Science.gov (United States)

    Gao, Xuanwen; Luo, Wenbin; Zhong, Chao; Wexler, David; Chou, Shu-Lei; Liu, Hua-Kun; Shi, Zhicong; Chen, Guohua; Ozawa, Kiyoshi; Wang, Jia-Zhao

    2014-08-29

    Nano-Germanium/polypyrrole composite has been synthesized by chemical reduction method in aqueous solution. The Ge nanoparticles were directly coated on the surface of the polypyrrole. The morphology and structural properties of samples were determined by X-ray diffraction, scanning electron microscopy and transmission electron microscopy. Thermogravimetric analysis was carried out to determine the polypyrrole content. The electrochemical properties of the samples have been investigated and their suitability as anode materials for the lithium-ion battery was examined. The discharge capacity of the Ge nanoparticles calculated in the Ge-polypyrrole composite is 1014 mAh g(-1) after 50 cycles at 0.2 C rate, which is much higher than that of pristine germanium (439 mAh g(-1)). The composite also demonstrates high specific discharge capacities at different current rates (1318, 1032, 661, and 460 mAh g(-1) at 0.5, 1.0, 2.0, and 4.0 C, respectively). The superior electrochemical performance of Ge-polypyrrole composite could be attributed to the polypyrrole core, which provides an efficient transport pathway for electrons. SEM images of the electrodes have demonstrated that polypyrrole can also act as a conductive binder and alleviate the pulverization of electrode caused by the huge volume changes of the nanosized germanium particles during Li(+) intercalation/de-intercalation.

  15. A review of atomic layer deposition providing high performance lithium sulfur batteries

    Science.gov (United States)

    Yan, Bo; Li, Xifei; Bai, Zhimin; Song, Xiaosheng; Xiong, Dongbin; Zhao, Mengli; Li, Dejun; Lu, Shigang

    2017-01-01

    With the significant obstacles that have been conquered in lithium-sulfur (Li-S) batteries, it is urgent to impel accelerating development of room-temperature Li-S batteries with high energy density and long-term stability. In view of the unique solid-liquid-solid conversion processes of Li-S batteries, however, designing effective strategies to address the insulativity and volume effect of cathode, shuttle of soluble polysulfides, and/or safety hazard of Li metal anode has been challenging. An atomic layer deposition (ALD) is a representative thin film technology with exceptional capabilities in developing atomic-precisely conformal films. It has been demonstrated to be a promise strategy of solving emerging issues in advanced electrical energy storage (EES) devices via the surface modification and/or the fabrication of complex nanostructured materials. In this review, the recent developments and significances on how ALD improves the performance of Li-S batteries were discussed in detail. Significant attention mainly focused on the various strategies with the use of ALD to refine the electrochemical interfaces and cell configurations. Furthermore, the novel opportunities and perspective associated with ALD for future research directions were summarized. This review may boost the development and application of advanced Li-S batteries using ALD.

  16. Pie-like electrode design for high-energy density lithium-sulfur batteries

    Science.gov (United States)

    Li, Zhen; Zhang, Jin Tao; Chen, Yu Ming; Li, Ju; Lou, Xiong Wen (David)

    2015-11-01

    Owing to the overwhelming advantage in energy density, lithium-sulfur (Li-S) battery is a promising next-generation electrochemical energy storage system. Despite many efforts in pursuing long cycle life, relatively little emphasis has been placed on increasing the areal energy density. Herein, we have designed and developed a `pie' structured electrode, which provides an excellent balance between gravimetric and areal energy densities. Combining lotus root-like multichannel carbon nanofibers `filling' and amino-functionalized graphene `crust', the free-standing paper electrode (S mass loading: 3.6 mg cm-2) delivers high specific capacity of 1,314 mAh g-1 (4.7 mAh cm-2) at 0.1 C (0.6 mA cm-2) accompanied with good cycling stability. Moreover, the areal capacity can be further boosted to more than 8 mAh cm-2 by stacking three layers of paper electrodes with S mass loading of 10.8 mg cm-2.

  17. Modeling the reduction of gross lithium erosion observed under high-flux deuterium bombardment

    Energy Technology Data Exchange (ETDEWEB)

    Abrams, T., E-mail: tabrams@pppl.gov [Princeton Plasma Physics Laboratory, Princeton, NJ 08543 (United States); Jaworski, M.A.; Kaita, R.; Nichols, J.H.; Stotler, D.P. [Princeton Plasma Physics Laboratory, Princeton, NJ 08543 (United States); De Temmerman, G.; Berg, M.A. van den; Meiden, H.J. van der; Morgan, T.W. [FOM Institute DIFFER – Dutch Institute for Fundamental Energy Research, Trilateral Euregio Cluster, Associate EURATOM-FOM, BL-3430 BE Nieuwegein (Netherlands)

    2015-08-15

    Both thin (<1 μm) and thick (∼500 μm) lithium films under high-flux deuterium and neon plasma bombardment were studied in the linear plasma device Magnum-PSI at ion fluxes >10{sup 24} m{sup −2} s{sup −1} and surface temperatures <700 °C. During Ne plasma exposures, Li erosion rates inferred from measurements of Li–I radiation exceed Langmuir Law evaporation, but no previous results exist to benchmark the binary collision approximation (BCA) and thermal sputtering measurements. Measured Li erosion rates during D plasma bombardment were compared to the adatom-evaporation model of thermal sputtering with an additional reduction term to account for the relative D/Li composition of the Li film. This model captures the qualitative evolution of the Li erosion yield but still overestimates the measured erosion by a factor of 5–10. This suggests that additional refinements to the mixed-material model are needed.

  18. Investigating the Effects of Anisotropic Mass Transport on Dendrite Growth in High Energy Density Lithium Batteries

    Energy Technology Data Exchange (ETDEWEB)

    Tan, Jinwang; Tartakovsky, Alexandre M.; Ferris, Kim F.; Ryan, Emily M.

    2016-01-01

    Dendrite formation on the electrode surface of high energy density lithium (Li) batteries causes safety problems and limits their applications. Suppressing dendrite growth could significantly improve Li battery performance. Dendrite growth and morphology is a function of the mixing in the electrolyte near the anode interface. Most research into dendrites in batteries focuses on dendrite formation in isotropic electrolytes (i.e., electrolytes with isotropic diffusion coefficient). In this work, an anisotropic diffusion reaction model is developed to study the anisotropic mixing effect on dendrite growth in Li batteries. The model uses a Lagrangian particle-based method to model dendrite growth in an anisotropic electrolyte solution. The model is verified by comparing the numerical simulation results with analytical solutions, and its accuracy is shown to be better than previous particle-based anisotropic diffusion models. Several parametric studies of dendrite growth in an anisotropic electrolyte are performed and the results demonstrate the effects of anisotropic transport on dendrite growth and morphology, and show the possible advantages of anisotropic electrolytes for dendrite suppression.

  19. Synergistic Ultrathin Functional Polymer-Coated Carbon Nanotube Interlayer for High Performance Lithium-Sulfur Batteries.

    Science.gov (United States)

    Kim, Joo Hyun; Seo, Jihoon; Choi, Junghyun; Shin, Donghyeok; Carter, Marcus; Jeon, Yeryung; Wang, Chengwei; Hu, Liangbing; Paik, Ungyu

    2016-08-10

    Lithium-sulfur (Li-S) batteries have been intensively investigated as a next-generation rechargeable battery due to their high energy density of 2600 W·h kg(-1) and low cost. However, the systemic issues of Li-S batteries, such as the polysulfide shuttling effect and low Coulombic efficiency, hinder the practical use in commercial rechargeable batteries. The introduction of a conductive interlayer between the sulfur cathode and separator is a promising approach that has shown the dramatic improvements in Li-S batteries. The previous interlayer work mainly focused on the physical confinement of polysulfides within the cathode part, without considering the further entrapment of the dissolved polysulfides. Here, we designed an ultrathin poly(acrylic acid) coated single-walled carbon nanotube (PAA-SWNT) film as a synergic functional interlayer to address the issues mentioned above. The designed interlayer not only lowers the charge transfer resistance by the support of the upper current collector but also localizes the dissolved polysulfides within the cathode part by the aid of a physical blocking and chemical bonding. With the synergic combination of PAA and SWNT, the sulfur cathode with a PAA-SWNT interlayer maintained higher capacity retention over 200 cycles and achieved better rate retention than the sulfur cathode with a SWNT interlayer. The proposed approach of combining a functional polymer and conductive support material can provide an optimiztic strategy to overcome the fundamental challenges underlying in Li-S batteries.

  20. Novel Ceramic-Grafted Separator with Highly Thermal Stability for Safe Lithium-Ion Batteries.

    Science.gov (United States)

    Jiang, Xiaoyu; Zhu, Xiaoming; Ai, Xinping; Yang, Hanxi; Cao, Yuliang

    2017-08-09

    The separator is a critical component of lithium-ion batteries (LIBs), which not only allows ionic transport while it prevents electrical contact between electrodes but also plays a key role for thermal safety performance of LIBs. However, commercial separators for LIBs are typically microporous polyolefin membranes that pose challenges for battery safety, due to shrinking and melting at elevated temperature. Here, we demonstrate a strategy to improve the thermal stability and electrolyte affinity of polyethylene (PE) separators. By simply grafting the vinylsilane coupling reagent on the surface of the PE separator by electron beam irradiation method and subsequent hydrolysis reaction into the Al(3+) solution, an ultrathin Al2O3 layer is grafted on the surface of the porous polymer microframework without sacrificing the porous structure and increasing the thickness. The as-synthesized Al2O3 ceramic-grafted separator (Al2O3-CGS) shows almost no shrinkage at 150 °C and decreases the contact angle of the conventional electrolyte compared with the bare PE separator. Notably, the full cells with the Al2O3-CGSs exhibit better cycling performance and rate capability and also provide stable open circuit voltage even at 170 °C, indicating its promising application in LIBs with high safety and energy density.

  1. Lithium and sodium storage in highly ordered mesoporous nitrogen-doped carbons derived from honey

    Science.gov (United States)

    Zhang, Yongzhi; Chen, Li; Meng, Yan; Xie, Jun; Guo, Yong; Xiao, Dan

    2016-12-01

    Honey, a widely existent biomass, consists mainly of carbohydrate and other nitrogen-containing substances such as proteins, enzymes and organic acids. It can be mixed homogeneously with mesoporous silica template for its excellent water-solubility and moderate viscosity. In this work, honey was employed as a nitrogen-containing carbon precursor to prepare nitrogen-doped ordered mesoporous carbons (OMCs). The obtained honey derived mesoporous nitrogen-doped carbons (HMNCs) with dilated interlayer spacings of 0.387-0.395 nm, narrow pore size distributions centering at around 4 nm and satisfactory N contents of 1.38-4.32 wt% offer superb dual functionality for lithium ion battery (LIB) and sodium ion battery (NIB) anodes. Tested against Li, the optimized HMNC-700 delivers a superior reversible capacity of 1359 mA h g-1 after 10 cycles at 100 mA g-1 and excellent rate capability and cycling stability of 722 mA h g-1 after 200 cycles at 1 A g-1. For NIB applications, HMNC-700 offers a high initial reversible capacity of 427 mA h g-1 and stable reversible capacity of 394 mA h g-1 at 100 mA g-1.

  2. Monodisperse mesoporous anatase beads as high performance and safer anodes for lithium ion batteries

    Science.gov (United States)

    Rodriguez, Erwin F.; Chen, Dehong; Hollenkamp, Anthony F.; Cao, Lu; Caruso, Rachel A.

    2015-10-01

    To achieve high efficiency lithium ion batteries (LIBs), an effective active material is important. In this regard, monodisperse mesoporous titania beads (MMTBs) featuring well interconnected nanoparticles were synthesised, and their mesoporous properties were tuned to study how these affect the electrochemical performance in LIBs. Two pore diameters of 15 and 25 nm, three bead diameters of 360, 800 and 2100 nm, and various annealing temperatures (from 300 to 650 °C) were investigated. The electrochemical results showed that while the pore size does not significantly influence the electrochemical behaviour, the specific surface area and the nanocrystal size affect the performance. Also, there is an optimum annealing temperature that enhances electron transfer across the titania bead structure. The carbon content employed in the electrode was varied, showing that the bead diameter strongly influences the minimal content of the conductive carbon required to fabricate the electrode. As a general rule, the smaller the bead diameter, the more carbon was required in the electrode. A large energy capacity and high current rate performance were achieved on the MMTBs featuring high surface area, nano-sized anatase crystals and well-sintered connections between the nanocrystals. The high stability of these mesoporous structures was demonstrated by charge/discharge cycling up to 500 cycles. Devices constructed with the MMTBs retained more than 80% of the initial capacity, indicating an excellent performance.To achieve high efficiency lithium ion batteries (LIBs), an effective active material is important. In this regard, monodisperse mesoporous titania beads (MMTBs) featuring well interconnected nanoparticles were synthesised, and their mesoporous properties were tuned to study how these affect the electrochemical performance in LIBs. Two pore diameters of 15 and 25 nm, three bead diameters of 360, 800 and 2100 nm, and various annealing temperatures (from 300 to 650

  3. N-doped graphene-SnO{sub 2} sandwich paper for high-performance lithium-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Xi; Chen, Shimou; Tang, Dai-Ming; Zhai, Tianyou; Li, Liang; Bando, Yoshio; Golberg, Dmitri [International Center for Young Scientists (ICYS) and International Center for Materials, Nanoarchitectonics (MANA), National Institute for Materials Science (NIMS), Namiki 1-1, Tsukuba, Ibaraki 305-0044 (Japan); Cao, Xinqiang; Zhong, Yeteng [Beijing National Laboratory for Molecular Science, Key Laboratory of Photochemistry, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190 (China); Bourgeois, Laure [Monash Centre for Electron Microscopy and Department of Materials Engineering, Monash University, VIC 3800 (Australia); Guan, Hasigaowa [Key Laboratory of Marine Chemistry Theory and Technology, Ministry of Education, Ocean University of China, Qingdao 266100 (China); Li, Huiqiao [Energy Technology Research Institute, National Institute of Advanced Industry and Technology (AIST), Umezono, 1-1-1, Tsukuba (Japan)

    2012-07-10

    A new facile route to fabricate N-doped graphene-SnO{sub 2} sandwich papers is developed. The 7,7,8,8-tetracyanoquinodimethane anion (TCNQ{sup -}) plays a key role for the formation of such structures as it acts as both the nitrogen source and complexing agent. If used in lithium-ion batteries (LIBs), the material exhibits a large capacity, high rate capability, and excellent cycling stability. The superior electrochemical performance of this novel material is the result from its unique features: excellent electronic conductivity related to the sandwich structure, short transportation length for both lithium ions and electrons, and elastomeric space to accommodate volume changes upon Li insertion/extraction. (Copyright copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  4. A Sulfur Heterocyclic Quinone Cathode and a Multifunctional Binder for a High-Performance Rechargeable Lithium-Ion Battery.

    Science.gov (United States)

    Ma, Ting; Zhao, Qing; Wang, Jianbin; Pan, Zeng; Chen, Jun

    2016-05-23

    We report a rational design of a sulfur heterocyclic quinone (dibenzo[b,i]thianthrene-5,7,12,14-tetraone=DTT) used as a cathode (uptake of four lithium ions to form Li4 DTT) and a conductive polymer [poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate)= PSS) used as a binder for a high-performance rechargeable lithium-ion battery. Because of the reduced energy level of the lowest unoccupied molecular orbital (LUMO) caused by the introduced S atoms, the initial Li-ion intercalation potential of DTT is 2.89 V, which is 0.3 V higher than that of its carbon analog. Meanwhile, there is a noncovalent interaction between DTT and PSS, which remarkably suppressed the dissolution and enhanced the conductivity of DTT, thus leading to the great improvement of the electrochemical performance. The DTT cathode with the PSS binder displays a long-term cycling stability (292 mAh g(-1) for the first cycle, 266 mAh g(-1) after 200 cycles at 0.1 C) and a high rate capability (220 mAh g(-1) at 1 C). This design strategy based on a noncovalent interaction is very effective for the application of small organic molecules as the cathode of rechargeable lithium-ion batteries. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  5. General synthesis of vanadium-based mixed metal oxides hollow nanofibers for high performance lithium-ion batteries

    Science.gov (United States)

    Xiang, Juan; Yu, Xin-Yao; Paik, Ungyu

    2016-10-01

    Hollow nanostructured mixed metal oxides have recently been intensively investigated as electrode materials for energy storage and conversion due to their remarkable electrochemical properties. Although great efforts have been made, the synthesis of hollow nanostructured vanadium-based mixed metal oxides especially those with one dimensional structure is rarely reported. Vanadium-based mixed metal oxides are promising electrode materials for lithium-ion batteries with high capacity and good rate capability. Here, we develop a facile and general method for the synthesis of one dimensional MxV2O8 (M = Co, Ni, Fe) tubular structure through a simple single-spinneret electrospinning technique followed by a calcination process. As a demonstration, Co3V2O8 hollow nanofibers are evaluated as anode materials for lithium-ion batteries. As expected, benefiting from their unique one dimensional tubular structure, the as-synthesized Co3V2O8 exhibits excellent electrochemical properties for lithium storage. To be specific, it can deliver a high specific capacity of 900 mAh g-1 at 5 A g-1, and long cycling stability up to 2000 cycles. The present work makes a significant contribution to the design and synthesis of mixed metal oxides with one dimensional tubular structure, as well as their potential applications in electrochemical energy storage.

  6. CNT Sheet Air Electrode for the Development of Ultra-High Cell Capacity in Lithium-Air Batteries

    Science.gov (United States)

    Nomura, Akihiro; Ito, Kimihiko; Kubo, Yoshimi

    2017-04-01

    Lithium-air batteries (LABs) are expected to provide a cell with a much higher capacity than ever attained before, but their prototype cells present a limited areal cell capacity of no more than 10 mAh cm-2, mainly due to the limitation of their air electrodes. Here, we demonstrate the use of flexible carbon nanotube (CNT) sheets as a promising air electrode for developing ultra-high capacity in LAB cells, achieving areal cell capacities of up to 30 mAh cm-2, which is approximately 15 times higher than the capacity of cells with lithium-ion battery (LiB) technology (~2 mAh cm-2). During discharge, the CNT sheet electrode experienced enormous swelling to a thickness of a few millimeters because of the discharge product deposition of lithium peroxide (Li2O2), but the sheet was fully recovered after being fully charged. This behavior results from the CNT sheet characteristics of the flexible and fibrous conductive network and suggests that the CNT sheet is an effective air electrode material for developing a commercially available LAB cell with an ultra-high cell capacity.

  7. Expanded graphite embedded with aluminum nanoparticles as superior thermal conductivity anodes for high-performance lithium-ion batteries

    Science.gov (United States)

    Zhao, Tingkai; She, Shengfei; Ji, Xianglin; Guo, Xinai; Jin, Wenbo; Zhu, Ruoxing; Dang, Alei; Li, Hao; Li, Tiehu; Wei, Bingqing

    2016-01-01

    The development of high capacity and long-life lithium-ion batteries is a long-term pursuing and under a close scrutiny. Most of the researches have been focused on exploring electrode materials and structures with high store capability of lithium ions and at the same time with a good electrical conductivity. Thermal conductivity of an electrode material will also have significant impacts on boosting battery capacity and prolonging battery lifetime, which is, however, underestimated. Here, we present the development of an expanded graphite embedded with Al metal nanoparticles (EG-MNPs-Al) synthesized by an oxidation-expansion process. The synthesized EG-MNPs-Al material exhibited a typical hierarchical structure with embedded Al metal nanoparticles into the interspaces of expanded graphite. The parallel thermal conductivity was up to 11.6 W·m−1·K−1 with a bulk density of 453 kg·m−3 at room temperature, a 150% improvement compared to expanded graphite (4.6 W·m−1·K−1) owing to the existence of Al metal nanoparticles. The first reversible capacity of EG-MNPs-Al as anode material for lithium ion battery was 480 mAh·g−1 at a current density of 100 mA·g−1, and retained 84% capacity after 300 cycles. The improved cycling stability and system security of lithium ion batteries is attributed to the excellent thermal conductivity of the EG-MNPs-Al anodes. PMID:27671848

  8. Porous membrane with high curvature, three-dimensional heat-resistance skeleton: a new and practical separator candidate for high safety lithium ion battery

    OpenAIRE

    Junli Shi; Yonggao Xia; Zhizhang Yuan; Huasheng Hu; Xianfeng Li; Huamin Zhang; Zhaoping Liu

    2015-01-01

    Separators with high reliability and security are in urgent demand for the advancement of high performance lithium ion batteries. Here, we present a new and practical porous membrane with three-dimension (3D) heat-resistant skeleton and high curvature pore structure as a promising separator candidate to facilitate advances in battery safety and performances beyond those obtained from the conventional separators. The unique material properties combining with the well-developed structural chara...

  9. High performance nickel-metal hydride and lithium-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Koehler, U.; Kruger, F.J.; Kuempers, J.; Maul, M.; Niggemann, E.; Schoenfelder, H.H. [VARTA Batterie AG, Kelkheim (Germany)

    1997-12-31

    The development of high performance traction batteries is a key issue for the future market acceptance of electric and hybrid vehicles. The Nickel-Metal Hydride (NiMH) system is besides Lithium-Ion (Li-Ion) the most promising battery system for electric vehicles. NiMH batteries have already penetrated the consumer market worldwide. Due to its high design flexibility and robustness the NiMH battery system is an ideal candidate for the whole range of battery applications from small consumer cells up to large traction batteries. Because of its high power capability for charging and discharging, the NiMH system is regarded as the optimum battery system for hybrid vehicles. VARTA is developing three different NiMH product lines: high energy, high power and ultra-high power cells. The specific energy of these products exceeds 80 Wh/kg (high energy cells) and a specific power of more than 1000 W/kg (ultra high power cells) can be achieved. The most prominent feature of the Li-Ion battery system is its high gravimetric and volumetric energy density. Although still in the early stage of development, large prismatic Li-Ion cells reach specific energies of more than 120 Wh/kg and energy densities over 300 Wh/l. There is a predicted potential for a further increase of the specific energy of more than 30% and for the energy density of above 60% during the next 4 years. The system works within a wide temperature range of {minus}20 to +60 C and can run up to 1200 cycles. The Li-Ion system represents the latest battery technology. It is expected to be the dominating technology for electric vehicles and aerospace applications. Therefore, VARTA has developed large prismatic cells up to 240 Wh employing low cost manganese spinell cathodes and carbon anodes. This talk describes VARTA`s high performance NiMH and Li-Ion cells as well as complete batteries.

  10. High performance Si/C@CNF composite anode for solid-polymer lithium-ion batteries

    Science.gov (United States)

    Si, Q.; Hanai, K.; Ichikawa, T.; Hirano, A.; Imanishi, N.; Yamamoto, O.; Takeda, Y.

    The electrochemical performance of a composite of nano-Si powder and a pyrolytic carbon of polyvinyl chloride (PVC) with carbon nanofiber (CNF) was examined as an anode for solid-polymer lithium-ion batteries. Nano-Si powder was firstly coated with carbon by pyrolysis of PVC and then mixed with CNF (referred to as Si/C@CNF) using a rotation mixer. The composite exhibited good cycling performance, but suffered from a large irreversible capacity loss of which the retention was less than 60%. In order to reduce the loss, a thin lithium sheet was attached to the Si/C@CNF electrode surface as a reducing agent. The irreversible capacity of the first cycle was lowered to as much as 0 mAh g -1 and after the third cycle, the lithium insertion and extraction efficiency was almost 100%. A reversible capacity of more than 1000 mAh g -1 was still maintained after 40 cycles.

  11. Graphene-wrapped sulfur nanospheres with ultra-high sulfur loading for high energy density lithium-sulfur batteries

    Science.gov (United States)

    Liu, Ya; Guo, Jinxin; Zhang, Jun; Su, Qingmei; Du, Gaohui

    2015-01-01

    Lithium-sulfur (Li-S) battery with high theoretical energy density is one of the most promising energy storage systems for electric vehicles and intermittent renewable energy. However, due to the poor conductivity of the active material, considerable weight of the electrode is occupied by the conductive additives. Here we report a graphene-wrapped sulfur nanospheres composite (S-nanosphere@G) with sulfur content up to 91 wt% as the high energy density cathode material for Li-S battery. The sulfur nanospheres with diameter of 400-500 nm are synthesized through a solution-based approach with the existence of polyvinylpyrrolidone (PVP). Then the sulfur nanospheres are uniformly wrapped by conductive graphene sheets through the electrostatic interaction between graphene oxide and PVP, followed by reducing of graphene oxide with hydrazine. The design of graphene wrapped sulfur nanoarchitecture provides flexible conductive graphene coating with void space to accommodate the volume expansion of sulfur and to minimize polysulfide dissolution. As a result, the S-nanosphere@G nanocomposite with 91 wt% sulfur shows a reversible initial capacity of 970 mA h g-1 and an average columbic efficiency > 96% over 100 cycles at a rate of 0.2 C. Taking the total mass of electrode into account, the S-nanosphere@G composite is a promising cathode material for high energy density Li-S batteries.

  12. Lithium Intoxication

    Directory of Open Access Journals (Sweden)

    Sermin Kesebir

    2011-09-01

    Full Text Available Lithium has been commonly used for the treatment of several mood disorders particularly bipolar disorder in the last 60 years. Increased intake and decreased excretion of lithium are the main causes for the development of lithium intoxication. The influence of lithium intoxication on body is evaluated as two different groups; reversible or irreversible. Irreversible damage is usually related with the length of time passed as intoxicated. Acute lithium intoxication could occur when an overdose of lithium is received mistakenly or for the purpose of suicide. Patients may sometimes take an overdose of lithium for self-medication resulting in acute intoxication during chronic, while others could develop chronic lithium intoxication during a steady dose treatment due to a problem in excretion of drug. In such situations, it is crucial to be aware of risk factors, to recognize early clinical symptoms and to conduct a proper medical monitoring. In order to justify or exclude the diagnosis, quantitative evaluation of lithium in blood and toxicologic screening is necessary. Following the monitoring schedules strictly and urgent intervention in case of intoxication would definitely reduce mortality and sequela related with lithium intoxication. In this article, the etiology, frequency, definition, clinical features and treatment approaches to the lithium intoxication have been briefly reviewed.

  13. Analysis of WWER-440 and PWR RPV welds surveillance data to compare irradiation damage evolution

    Energy Technology Data Exchange (ETDEWEB)

    Debarberis, L. [Joint Research Centre of the European Commission, Institute for Energy, P.O. Box 2, 1755 ZG Petten (Netherlands)]. E-mail: luigi.debarberis@cec.eu.int; Acosta, B. [Joint Research Centre of the European Commission, Institute for Energy, P.O. Box 2, 1755 ZG Petten (Netherlands)]. E-mail: beatriz.acosta-iborra@jrc.nl; Zeman, A. [Joint Research Centre of the European Commission, Institute for Energy, P.O. Box 2, 1755 ZG Petten (Netherlands); Sevini, F. [Joint Research Centre of the European Commission, Institute for Energy, P.O. Box 2, 1755 ZG Petten (Netherlands); Ballesteros, A. [Tecnatom, Avd. Montes de Oca 1, San Sebasitan de los Reyes, E-28709 Madrid (Spain); Kryukov, A. [Russian Research Centre Kurchatov Institute, Kurchatov Square 1, 123182 Moscow (Russian Federation); Gillemot, F. [AEKI Atomic Research Institute, Konkoly Thege M. ut 29-33, 1121 Budapest (Hungary); Brumovsky, M. [NRI, Nuclear Research Institute, Husinec-Rez 130, 25068 Rez (Czech Republic)

    2006-04-15

    It is known that for Russian-type and Western water reactor pressure vessel steels there is a similar degradation in mechanical properties during equivalent neutron irradiation. Available surveillance results from WWER and PWR vessels are used in this article to compare irradiation damage evolution for the different reactor pressure vessel welds. The analysis is done through the semi-mechanistic model for radiation embrittlement developed by JRC-IE. Consistency analysis with BWR vessel materials and model alloys has also been performed within this study. Globally the two families of studied materials follow similar trends regarding the evolution of irradiation damage. Moreover in the high fluence range typical of operation of WWER the radiation stability of these vessels is greater than the foreseen one for PWR.

  14. Proving test on the seismic reliability of nuclear power plant: PWR reactor containment vessel

    Energy Technology Data Exchange (ETDEWEB)

    Akiyama, Hiroshi; Yoshikawa, Teiichi; Ohno, Tokue; Yoshikawa, Eiji.

    1989-01-01

    Seismic reliability proving tests of nuclear power plant facilities are carried out by the Nuclear Power Engineering Test Center, using the large-scale, high-performance vibration table of Tadotsu Engineering Laboratory, and sponsored by the Ministry of International Trade and Industry. In 1982, the seismic reliability proving test of a PWR containment vessel was conducted using a test component of reduced scale 1/3.7. As a result of this test, the test component proved to have structural soundness against earthquakes, and at the same time its stable function was proved by leak tests which were carried out before and after the vibration test. In 1983, the detailed analysis and evaluation of these test results were carried out, and the analysis methods for evaluating strength against earthquakes were established. The seismic analysis and evaluation on the actual containment vessel were then performed using these analysis methods, and the safety and reliability of the PWR reactor containment vessel were confirmed.

  15. Characterization of Factors affecting IASCC of PWR Core Internals

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Sung Woo; Hwang, Seong Sik; Kim, Won Sam [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)

    2008-09-15

    A lot works have been performed on IASCC in BWR. Recent efforts have been devoted to investigate IASCC in PWR, but the mechanism in PWR is not fully understood yet as compared with that in BWR due to a lack of data from laboratories and fields. Therefore it is strongly needed to review and analyse recent researches of IASCC in both BWR and PWR for establishing a proactive management technology for IASCC of core internals in Korean PWRs. This work is aimed to review mainly recent technical reports on IASCC of stainless steels for core internals in PWR. For comparison, the works on IASCC in BWR were also reviewed and briefly introduced in this report.

  16. The PWR cores management; La gestion des coeurs REP

    Energy Technology Data Exchange (ETDEWEB)

    Barral, J.C. [Electricite de France (EDF), 75 - Paris (France); Rippert, D. [CEA Cadarache, Departement d' Etudes des Reacteurs, DER, 13 - Saint-Paul-lez-Durance (France); Johner, J. [CEA/Cadarache, Dept. de Recherches sur la Fusion Controlee, DRFC, 13 - Saint-Paul-lez-Durance (France)] [and others

    2000-01-25

    During the meeting of the 25 january 2000, organized by the SFEN, scientists and plant operators in the domain of the PWR debated on the PWR cores management. The five first papers propose general and economic information on the PWR and also the fast neutron reactors chains in the electric power market: statistics on the electric power industry, nuclear plant unit management, the ITER project and the future of the thermonuclear fusion, the treasurer's and chairman's reports. A second part offers more technical papers concerning the PWR cores management: performance and optimization, in service load planning, the cores management in the other countries, impacts on the research and development programs. (A.L.B.)

  17. Morphology control of ordered mesoporous carbons for high capacity lithium sulfur batteries

    Energy Technology Data Exchange (ETDEWEB)

    Schuster, Joerg David

    2011-06-07

    The focus of this thesis concerns the morphology control of ordered mesoporous carbon (OMC) materials. Ordered mesoporous carbons with diverse morphologies, that are thin films, fibers - embedded in anodic alumina membranes and free-standing - or spherical nanoparticles, have been successfully prepared by soft-templating procedures. The mechanisms of structure formation and processing were investigated with in-situ SAXS measurements and their application in high capacity lithium-sulfur batteries was successfully tested in cooperation with Guang He and Linda Nazar from the University of Waterloo in Canada. The Li-S batteries receive increasing attention due to their high theoretical energy density which is 3 to 5 times higher than from lithium-ion batteries. For this type of battery the specific pore volume is crucial for the content of the active component (sulfur) in the cathode and therefore correlates with the capacity and gravimetric energy density of the battery. At first, mesoporous thin films with 2D-hexagonal structure were obtained through organic-organic self-assembly of a preformed oligomeric resol precursor and the triblock copolymer template Pluronic P123. The formation of a condensed-wall material through thermopolymerization of the precursor oligomers resulted in mesostructured phenolic resin films. Subsequent decomposition of the surfactant and partial carbonization were achieved through thermal treatment in inert atmosphere. The films were crack-free with tunable homogenous thicknesses, and showed either 2D-hexagonal or lamellar mesostructure. An additional, yet unknown 3D-mesostructure was also found. In the second part, cubic and circular hexagonal mesoporous carbon phases in the confined environment of tubular anodic alumina membrane (AAM) pores were obtained by self-assembly of the mentioned resol precursor and the triblock copolymer templates Pluronic F127 or P123, respectively. Casting and solvent-evaporation were also followed by

  18. Origins of Large Voltage Hysteresis in High-Energy-Density Metal Fluoride Lithium-Ion Battery Conversion Electrodes.

    Science.gov (United States)

    Li, Linsen; Jacobs, Ryan; Gao, Peng; Gan, Liyang; Wang, Feng; Morgan, Dane; Jin, Song

    2016-03-02

    Metal fluorides and oxides can store multiple lithium ions through conversion chemistry to enable high-energy-density lithium-ion batteries. However, their practical applications have been hindered by an unusually large voltage hysteresis between charge and discharge voltage profiles and the consequent low-energy efficiency (hysteresis are rarely studied and poorly understood. Here we employ in situ X-ray absorption spectroscopy, transmission electron microscopy, density functional theory calculations, and galvanostatic intermittent titration technique to first correlate the voltage profile of iron fluoride (FeF3), a representative conversion electrode material, with evolution and spatial distribution of intermediate phases in the electrode. The results reveal that, contrary to conventional belief, the phase evolution in the electrode is symmetrical during discharge and charge. However, the spatial evolution of the electrochemically active phases, which is controlled by reaction kinetics, is different. We further propose that the voltage hysteresis in the FeF3 electrode is kinetic in nature. It is the result of ohmic voltage drop, reaction overpotential, and different spatial distributions of electrochemically active phases (i.e., compositional inhomogeneity). Therefore, the large hysteresis can be expected to be mitigated by rational design and optimization of material microstructure and electrode architecture to improve the energy efficiency of lithium-ion batteries based on conversion chemistry.

  19. Monolayer MoS2-Graphene Hybrid Aerogels with Controllable Porosity for Lithium-Ion Batteries with High Reversible Capacity.

    Science.gov (United States)

    Jiang, Lianfu; Lin, Binghui; Li, Xiaoming; Song, Xiufeng; Xia, Hui; Li, Liang; Zeng, Haibo

    2016-02-03

    Monolayer MoS2 nanosheets (NSs) are promising anode materials for lithium-ion batteries because all redox reactions take place at the surface without lithium-ion diffusion limit. However, the expanded band gap of monolayer MoS2 NSs (∼1.8 eV) compared to their bulk counterparts (∼1.2 eV) and restacking tendency due to the van der Waals forces result in poor electron transfer and loss of the structure advantage. Here, a facile approach is developed to fabricate the MoS2-graphene aerogels comprising controlled three-dimensional (3D) porous architectures constructed by interconnected monolayer MoS2-graphene hybrid NSs. The robust 3D architectures combining with the monolayer feature of the hybrid NSs not only prevent the MoS2 and graphene NSs from restacking, but also enable fast electrode kinetics due to the surface reaction mechanism and highly conductive graphene matrix. As a consequence, the 3D porous monolayer MoS2-graphene composite aerogels exhibit a large reversible capacity up to 1200 mAh g(-1) as well as outstanding cycling stability and rate performance, making them promising as advanced anode materials for lithium-ion batteries.

  20. A Facile Bottom-Up Approach to Construct Hybrid Flexible Cathode Scaffold for High-Performance Lithium-Sulfur Batteries.

    Science.gov (United States)

    Ghosh, Arnab; Manjunatha, Revanasiddappa; Kumar, Rajat; Mitra, Sagar

    2016-12-14

    Lithium-sulfur batteries mostly suffer from the low utilization of sulfur, poor cycle life, and low rate performances. The prime factors that affect the performance are enormous volume change of the electrode, soluble intermediate product formation, poor electronic and ionic conductivity of S, and end discharge products (i.e., Li2S2 and Li2S). The attractive way to mitigate these challenges underlying in the fabrication of a sulfur nanocomposite electrode consisting of different nanoparticles with distinct properties of lithium storage capability, mechanical reinforcement, and ionic as well as electronic conductivity leading to a mechanically robust and mixed conductive (ionic and electronic conductive) sulfur electrode. Herein, we report a novel bottom-up approach to synthesize a unique freestanding, flexible cathode scaffold made of porous reduced graphene oxide, nanosized sulfur, and Mn3O4 nanoparticles, and all are three-dimensionally interconnected to each other by hybrid polyaniline/sodium alginate (PANI-SA) matrix to serve individual purposes. A capacity of 1098 mAh g(-1) is achieved against lithium after 200 cycles at a current rate of 2 A g(-1) with 97.6% of initial capacity at a same current rate, suggesting the extreme stability and cycling performance of such electrode. Interestingly, with the higher current density of 5 A g(-1), the composite electrode exhibited an initial capacity of 1015 mA h g(-1) and retained 71% of the original capacity after 500 cycles. The in situ Raman study confirms the polysulfide absorption capability of Mn3O4. This work provides a new strategy to design a mechanically robust, mixed conductive nanocomposite electrode for high-performance lithium-sulfur batteries and a strategy that can be used to develop flexible large power storage devices.

  1. Degraded core analysis for the PWR

    Energy Technology Data Exchange (ETDEWEB)

    Gittus, J.H.

    1987-10-01

    The paper presents an analysis of the probability and consequences of degraded core accidents for the PWR. The article is based on a paper which was presented by the author to the Sizewell-B public inquiry. Degraded core accidents are examined with respect to:- the initiating events, safety plant failure, and processes with a bearing on containment failure. Accident types and frequencies are discussed, as well as the dispersion of radionuclides. Accident risks, i.e. individual and societal risks in degraded core accidents are assessed from:- the amount of radionuclides released, the weather, the population distribution, and the accident frequencies. Uncertainties in the assessment of degraded core accidents are also summarized. (U.K.).

  2. A pressure drop model for PWR grids

    Energy Technology Data Exchange (ETDEWEB)

    Oh, Dong Seok; In, Wang Ki; Bang, Je Geon; Jung, Youn Ho; Chun, Tae Hyun [Korea Atomic Energy Research Institute, Taejon (Korea, Republic of)

    1998-12-31

    A pressure drop model for the PWR grids with and without mixing device is proposed at single phase based on the fluid mechanistic approach. Total pressure loss is expressed in additive way for form and frictional losses. The general friction factor correlations and form drag coefficients available in the open literatures are used to the model. As the results, the model shows better predictions than the existing ones for the non-mixing grids, and reasonable agreements with the available experimental data for mixing grids. Therefore it is concluded that the proposed model for pressure drop can provide sufficiently good approximation for grid optimization and design calculation in advanced grid development. 7 refs., 3 figs., 3 tabs. (Author)

  3. High-density sodium and lithium ion battery anodes from banana peels.

    Science.gov (United States)

    Lotfabad, Elmira Memarzadeh; Ding, Jia; Cui, Kai; Kohandehghan, Alireza; Kalisvaart, W Peter; Hazelton, Michael; Mitlin, David

    2014-07-22

    Banana peel pseudographite (BPPG) offers superb dual functionality for sodium ion battery (NIB) and lithium ion battery (LIB) anodes. The materials possess low surface areas (19-217 m(2) g(-1)) and a relatively high electrode packing density (0.75 g cm(-3) vs ∼1 g cm(-3) for graphite). Tested against Na, BPPG delivers a gravimetric (and volumetric) capacity of 355 mAh g(-1) (by active material ∼700 mAh cm(-3), by electrode volume ∼270 mAh cm(-3)) after 10 cycles at 50 mA g(-1). A nearly flat ∼200 mAh g(-1) plateau that is below 0.1 V and a minimal charge/discharge voltage hysteresis make BPPG a direct electrochemical analogue to graphite but with Na. A charge capacity of 221 mAh g(-1) at 500 mA g(-1) is degraded by 7% after 600 cycles, while a capacity of 336 mAh g(-1) at 100 mAg(-1) is degraded by 11% after 300 cycles, in both cases with ∼100% cycling Coulombic efficiency. For LIB applications BPPG offers a gravimetric (volumetric) capacity of 1090 mAh g(-1) (by material ∼2200 mAh cm(-3), by electrode ∼900 mAh cm(-3)) at 50 mA g(-1). The reason that BPPG works so well for both NIBs and LIBs is that it uniquely contains three essential features: (a) dilated intergraphene spacing for Na intercalation at low voltages; (b) highly accessible near-surface nanopores for Li metal filling at low voltages; and (c) substantial defect content in the graphene planes for Li adsorption at higher voltages. The underpotential deposition. By contrast, the same analysis proves the presence of metallic Li in the pores, with intercalation being much less pronounced.

  4. High performance nickel-metal hydride and lithium-ion batteries

    Science.gov (United States)

    Köhler, U.; Kümpers, J.; Ullrich, M.

    In comparison to pure electric vehicles (EV) the opportunities for hybrid electric vehicles (HEV) are much better, since range restrictions no longer apply and the interaction of the internal combustion engine and electrical drive bring increased energy efficiency and environmental friendliness. The batteries used in such applications must meet very high standards in terms of performance and service life. Although the battery capacity is smaller than for a purely EV, it needs to be able to generate far higher levels of power. The technical challenges of hybrid applications have led to the development of high-performance batteries. At the forefront of these is the nickel-metal hydride system (NiMH). With specific power and energy data in the range from 300 to 900 W/kg, 55 to 37 Wh/kg, respectively (based on cell weight), excellent charge efficiency and energy throughput levels of more than 10,000 times the nominal energy, the NiMH system comes very close to satisfying the needs of the HEV. Parallel developments with the lithium-ion system based on manganese spinel as cathode material show that, with specific power and energy levels above 1000 W/kg, 50 Wh/kg, respectively, this technology will also be able to play an important role in the future. Service life figures in terms of calendar life have been improved tremendously to about three years, but there is still a need for further improvement in order to meet the specifications of car manufacturers. For this reason, an increase of life span is the subject of intensive development work.

  5. Design of poly(acrylonitrile)-based gel electrolytes for high-performance lithium ion batteries.

    Science.gov (United States)

    Wang, Shih-Hong; Kuo, Ping-Lin; Hsieh, Chien-Te; Teng, Hsisheng

    2014-11-12

    The use of polyacrylonitrile (PAN) as a host for gel polymer electrolytes (GPEs) commonly produces a strong dipole-dipole interaction with the polymer. This study presents a strategy for the application of PAN in GPEs for the production of high performance lithium ion batteries. The resulting gel electrolyte GPE-AVM comprises a poly(acrylonitrile-co-vinyl acetate) copolymer blending poly(methyl methacrylate) as a host, which is swelled using a liquid electrolyte (LE) of 1 M LiPF6 in carbonate solvent. Vinyl acetate and methacrylate groups segregate the PAN chains in the GPE, which produces high ionic conductivity (3.5 × 10 (-3) S cm(-1) at 30 °C) and a wide electrochemical voltage range (>6.5 V) as well as an excellent Li(+) transference number of 0.6. This study includes GPE-AVM in a full-cell battery comprising a LiFePO4 cathode and graphite anode to promote ion motion, which reduced resistance in the battery by 39% and increased the specific power by 110%, relative to the performance of batteries based on LE. The proposed GPE-based battery has a capacity of 140 mAh g(-1) at a discharge rate of 0.1 C and is able to deliver 67 mAh g(-1) of electricity at 17 C. The proposed GPE-AVM provides a robust interface with the electrodes in full-cell batteries, resulting in 93% capacity retention after 100 charge-discharge cycles at 17 C and 63% retention after 1000 cycles.

  6. Mechanisms for electrochemical performance enhancement by the salt-type electrolyte additive, lithium difluoro(oxalato)borate, in high-voltage lithium-ion batteries

    Science.gov (United States)

    Cha, Jiho; Han, Jung-Gu; Hwang, Jaeseong; Cho, Jaephil; Choi, Nam-Soon

    2017-07-01

    Lithium difluoro(oxalato)borate (LiDFOB) with one oxalate moiety bonded to a central boron core was employed as a salt-type additive to enhance the interfacial stabilities of high-voltage Li-rich cathodes and graphite anodes. Our investigation revealed that the LiDFOB additive modified the surface film on the electrodes and effectively restrained degradation of the cycling performance of the electrodes. Investigation of the surface chemistries of the electrodes confirmed that LiDFOB produces a LiF-less surface film on the Li-rich cathode and a LiF-rich surface film on the graphite anode. Moreover, the use of 1% LiDFOB drastically improved the rate capabilities of Li-rich cathodes and graphite anodes. Within 100 cycles at a rate of C/2 at 25 °C, only 45.8% of the initial discharge capacity of a high-voltage Li-rich/graphite full cell was delivered in the baseline electrolyte, while the LiDFOB-containing electrolyte retained 82.7%.

  7. Porous membrane with high curvature, three-dimensional heat-resistance skeleton: a new and practical separator candidate for high safety lithium ion battery.

    Science.gov (United States)

    Shi, Junli; Xia, Yonggao; Yuan, Zhizhang; Hu, Huasheng; Li, Xianfeng; Zhang, Huamin; Liu, Zhaoping

    2015-02-05

    Separators with high reliability and security are in urgent demand for the advancement of high performance lithium ion batteries. Here, we present a new and practical porous membrane with three-dimension (3D) heat-resistant skeleton and high curvature pore structure as a promising separator candidate to facilitate advances in battery safety and performances beyond those obtained from the conventional separators. The unique material properties combining with the well-developed structural characteristics enable the 3D porous skeleton to own several favorable properties, including superior thermal stability, good wettability with liquid electrolyte, high ion conductivity and internal short-circuit protection function, etc. which give rise to acceptable battery performances. Considering the simply and cost-effective preparation process, the porous membrane is deemed to be an interesting direction for the future lithium ion battery separator.

  8. Porous membrane with high curvature, three-dimensional heat-resistance skeleton: a new and practical separator candidate for high safety lithium ion battery

    Science.gov (United States)

    Shi, Junli; Xia, Yonggao; Yuan, Zhizhang; Hu, Huasheng; Li, Xianfeng; Zhang, Huamin; Liu, Zhaoping

    2015-01-01

    Separators with high reliability and security are in urgent demand for the advancement of high performance lithium ion batteries. Here, we present a new and practical porous membrane with three-dimension (3D) heat-resistant skeleton and high curvature pore structure as a promising separator candidate to facilitate advances in battery safety and performances beyond those obtained from the conventional separators. The unique material properties combining with the well-developed structural characteristics enable the 3D porous skeleton to own several favorable properties, including superior thermal stability, good wettability with liquid electrolyte, high ion conductivity and internal short-circuit protection function, etc. which give rise to acceptable battery performances. Considering the simply and cost-effective preparation process, the porous membrane is deemed to be an interesting direction for the future lithium ion battery separator. PMID:25653104

  9. Morphology control of ordered mesoporous carbons for high capacity lithium sulfur batteries

    Energy Technology Data Exchange (ETDEWEB)

    Schuster, Joerg David

    2011-06-07

    The focus of this thesis concerns the morphology control of ordered mesoporous carbon (OMC) materials. Ordered mesoporous carbons with diverse morphologies, that are thin films, fibers - embedded in anodic alumina membranes and free-standing - or spherical nanoparticles, have been successfully prepared by soft-templating procedures. The mechanisms of structure formation and processing were investigated with in-situ SAXS measurements and their application in high capacity lithium-sulfur batteries was successfully tested in cooperation with Guang He and Linda Nazar from the University of Waterloo in Canada. The Li-S batteries receive increasing attention due to their high theoretical energy density which is 3 to 5 times higher than from lithium-ion batteries. For this type of battery the specific pore volume is crucial for the content of the active component (sulfur) in the cathode and therefore correlates with the capacity and gravimetric energy density of the battery. At first, mesoporous thin films with 2D-hexagonal structure were obtained through organic-organic self-assembly of a preformed oligomeric resol precursor and the triblock copolymer template Pluronic P123. The formation of a condensed-wall material through thermopolymerization of the precursor oligomers resulted in mesostructured phenolic resin films. Subsequent decomposition of the surfactant and partial carbonization were achieved through thermal treatment in inert atmosphere. The films were crack-free with tunable homogenous thicknesses, and showed either 2D-hexagonal or lamellar mesostructure. An additional, yet unknown 3D-mesostructure was also found. In the second part, cubic and circular hexagonal mesoporous carbon phases in the confined environment of tubular anodic alumina membrane (AAM) pores were obtained by self-assembly of the mentioned resol precursor and the triblock copolymer templates Pluronic F127 or P123, respectively. Casting and solvent-evaporation were also followed by

  10. Effect of proton irradiation on irradiation assisted stress corrosion cracking in PWR

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Han Ok; Hwang, Mi Jin; Kim, Sung Woo; Hwang, Seong Sik [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)

    2014-05-15

    Irradiation assisted stress corrosion cracking (IASCC) involves the cracking and failure of materials under irradiation environment in nuclear power plant water environment. The major factors and processes governing an IASCC are suggested by others. The IASCC of the reactor core internals due to the material degradation and the water chemistry change has been reported in high stress stainless steel components, such as fuel elements (Boiling Water Reactors) in the 1960s, a control rod in the 1970s, and a baffle former bolt in recent years of light water reactors (Pressurized Water Reactors). Many irradiated stainless steels that are resistant to inergranular cracking in 288 .deg. C argon are susceptible to IG cracking in the simulated BWR environment at the same temperature. Under the circumstances, a lot works have been performed on IASCC in BWR. Recent efforts have been devoted to investigate an IASCC in a PWR, but the mechanism in a PWR is not fully understood yet as compared with that in a BWR owing to a lack of data from laboratories and fields. Therefore, it is strongly necessary to review and analyze recent researches of an IASCC in both BWR and PWR for establishing a proactive management technology for the IASCC of core internals in Korean PWRs. The objective of this research to find IASCC behavior of proton irradiated 316 stainless steels in a high-temperature water chemistry environment. The IASCC initiation susceptibility on 1, 3, 5 DPA proton irradiated 316 austenite stainless steel was evaluated in PWR environment. SCC area ratio on the fracture surface was similar regardless of irradiation level. Total crack length on the irradiated surface increases in order of specimen 1, 3, 5 DPA. The total crack length at the side surface is a better measure in evaluating IASCC initiation susceptibility for proton-irradiated samples.

  11. Nano-sized structured layered positive electrode materials to enable high energy density and high rate capability lithium batteries

    Science.gov (United States)

    Deng, Haixia; Belharouak, Ilias; Amine, Khalil

    2012-10-02

    Nano-sized structured dense and spherical layered positive active materials provide high energy density and high rate capability electrodes in lithium-ion batteries. Such materials are spherical second particles made from agglomerated primary particles that are Li.sub.1+.alpha.(Ni.sub.xCo.sub.yMn.sub.z).sub.1-tM.sub.tO.sub.2-dR.sub.d- , where M is selected from can be Al, Mg, Fe, Cu, Zn, Cr, Ag, Ca, Na, K, In, Ga, Ge, V, Mo, Nb, Si, Ti, Zr, or a mixture of any two or more thereof, R is selected from F, Cl, Br, I, H, S, N, or a mixture of any two or more thereof, and 0.ltoreq..alpha..ltoreq.0.50; 0

  12. Lithium Abundance of Metal-poor Stars

    Institute of Scientific and Technical Information of China (English)

    Hua-Wei Zhang; Gang Zhao

    2003-01-01

    High-resolution, high signal-to-noise ratio spectra have been obtained for 32 metal-poor stars. The equivalent widths of Li λ6708A were measured and the lithium abundances were derived. The average lithium abundance of 21 stars on the lithium plateau is 2.33±0.02 dex. The Lithium plateau exhibits a marginal trend along metallicity, dA(Li)/d[Fe/H] = 0.12±0.06, and no clear trend with the effective temperature. The trend indicates that the abundance of lithium plateau may not be primordial and that a part of the lithium was produced in Galactic Chemical Evolution (GCE).

  13. Achieving high capacity and rate capability in layered lithium transition metal oxide cathodes for lithium-ion batteries

    Science.gov (United States)

    Ahn, Juhyeon; Susanto, Dieky; Noh, Jae-Kyo; Ali, Ghulam; Cho, Byung Won; Chung, Kyung Yoon; Kim, Jong Hak; Oh, Si Hyoung

    2017-08-01

    In this study, we target to find a new composition for a layered mixed metal oxide, which has a high structural stability and a good electrochemical performance. Our strategy is to alter the transition metal composition focusing on the relative amounts of redox active Ni and Co to the inactive Mn, based on highly-stabilized LiNi1/3Co1/3Mn1/3O2. X-ray absorption near-edge structure and X-ray diffraction analyses show that the degree of cation disorder decreases on increasing the ratio of Ni and Co to Mn, by the presence of Ni3+, suggesting that slightly higher Ni and Co contents lead to improved structural stability. Electrochemical studies demonstrate that LiNi0.4Co0.4Mn0.2O2 cathodes exhibit considerable improvements in both the reversible capacity and the rate capabilities at a voltage range of 2.5-4.6 V. In situ XRD measurements reveal that LiNi0.4Co0.4Mn0.2O2 maintains a single-phase and undergoes lesser structural variations compared to controlled compositions during a delithiation process up to 4.6 V, while achieving a high reversible capacity over 200 mAh g-1. As a result, LiNi0.4Co0.4Mn0.2O2 experiences fewer structural degradations during electrochemical cycling, which explains the excellent long-term cycling performance.

  14. Facile synthesis of one-dimensional zinc vanadate nanofibers for high lithium storage anode material

    Energy Technology Data Exchange (ETDEWEB)

    Luo, Lei [Key Laboratory of Eco-textiles, Ministry of Education, Jiangnan University, Wuxi 214122 (China); International Joint Research Laboratory for Advanced Functional Textile Materials, Jiangnan University, Wuxi 214122 (China); Fei, Yaqian; Chen, Ke; Li, Dawei; Wang, Xin [Key Laboratory of Eco-textiles, Ministry of Education, Jiangnan University, Wuxi 214122 (China); Wang, Qingqing [Key Laboratory of Eco-textiles, Ministry of Education, Jiangnan University, Wuxi 214122 (China); International Joint Research Laboratory for Advanced Functional Textile Materials, Jiangnan University, Wuxi 214122 (China); Wei, Qufu, E-mail: qfwei@jiangnan.edu.cn [Key Laboratory of Eco-textiles, Ministry of Education, Jiangnan University, Wuxi 214122 (China); International Joint Research Laboratory for Advanced Functional Textile Materials, Jiangnan University, Wuxi 214122 (China); Qiao, Hui [Key Laboratory of Eco-textiles, Ministry of Education, Jiangnan University, Wuxi 214122 (China)

    2015-11-15

    One-dimensional (1D) zinc vanadate (α-Zn{sub 2}V{sub 2}O{sub 7}) nanofibers have been synthesized through electrospinning combined with an annealing process. When used as anode material for lithium-ion batteries (LIBs), electrospun 1D α-Zn{sub 2}V{sub 2}O{sub 7} nanofibers exhibit a reversible capacity of ∼708 mAh g{sup −1} after 100 cycles at a current density of 50 mA g{sup −1}. A good rate capability is also achieved even at higher current densities. When cycled at a current density of 2000 mA g{sup −1}, the electrode can still show a reversible capacity of ∼311 mAh g{sup −1}. The excellent cycle performance and rate capability may be due to the 1D nanofiber architectures, mesoporous structures, and relatively large specific surface area, which can provide a short ion diffusion path and continuous electron transportation. Therefore, this work presents a simple and efficient approach for fabrication of 1D α-Zn{sub 2}V{sub 2}O{sub 7} nanofibers, which are promising high-performance anode materials for LIBs. - Highlights: • Electrospun 1D α-Zn{sub 2}V{sub 2}O{sub 7} nanofibers are first synthesized for anode material. • The electrochemical reaction mechanism of this material is discussed. • A reversible capacity of ∼708 mAh g{sup −1} is obtained after 100 cycles at 50 mA g{sup −1}. • 1D α-Zn{sub 2}V{sub 2}O{sub 7} nanofiber anodes show excellent rate capability for LIBs.

  15. Primate response to angiotensin infusion and high sodium intake differ by sodium lithium countertransport phenotype

    NARCIS (Netherlands)

    Spradling-Reeves, K.D.; Shade, R.E.; Haywood, J.R.; Cox, L.A.E.

    2017-01-01

    An increased level of sodium-lithium countertransport (SLC) activity has been associated with salt-sensitive hypertension. Previous findings have suggested that dysregulation of the renin-angiotensin-aldosterone system (RAAS) may be involved in the mechanism linking elevated SLC activity and hyperte

  16. High-capacity nanostructured germanium-containing materials and lithium alloys thereof

    Science.gov (United States)

    Graetz, Jason A.; Fultz, Brent T.; Ahn, Channing; Yazami, Rachid

    2010-08-24

    Electrodes comprising an alkali metal, for example, lithium, alloyed with nanostructured materials of formula Si.sub.zGe.sub.(z-1), where 0capacities, cycle lives, and/or cycling rates compared with similar electrodes made from graphite. These electrodes are useful as anodes for secondary electrochemical cells, for example, batteries and electrochemical supercapacitors.

  17. Advanced separators based on aromatic polymer for high energy density lithium batteries

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Zhengcheng; Woo, Jung-Je; Amine, Khalil

    2017-03-21

    A process includes casting a solution including poly(phenylene oxide), inorganic nanoparticles, a solvent, and a non-solvent on a substrate; and removing the solvent to form a porous film; wherein: the porous film is configured for use as a porous separator for a lithium ion battery.

  18. Hydrogen, lithium, and lithium hydride production

    Energy Technology Data Exchange (ETDEWEB)

    Brown, Sam W.; Spencer, Larry S.; Phillips, Michael R.; Powell, G. Louis; Campbell, Peggy J.

    2017-06-20

    A method is provided for extracting hydrogen from lithium hydride. The method includes (a) heating lithium hydride to form liquid-phase lithium hydride; (b) extracting hydrogen from the liquid-phase lithium hydride, leaving residual liquid-phase lithium metal; (c) hydriding the residual liquid-phase lithium metal to form refined lithium hydride; and repeating steps (a) and (b) on the refined lithium hydride.

  19. Graphene-Wrapped Sulfur Particles as a Rechargeable Lithium-Sulfur Battery Cathode Material with High Capacity and Cycling Stability

    Science.gov (United States)

    Wang, Hailiang; Yang, Yuan; Liang, Yongye; Robinson, Joshua Tucker; Li, Yanguang; Jackson, Ariel; Cui, Yi; Dai, Hongjie

    2011-07-01

    We report the synthesis of a graphene-sulfur composite material by wrapping polyethyleneglycol (PEG) coated submicron sulfur particles with mildly oxidized graphene oxide sheets decorated by carbon black nanoparticles. The PEG and graphene coating layers are important to accommodating volume expansion of the coated sulfur particles during discharge, trapping soluble polysulfide intermediates and rendering the sulfur particles electrically conducting. The resulting graphene-sulfur composite showed high and stable specific capacities up to ~600mAh/g over more than 100 cycles, representing a promising cathode material for rechargeable lithium batteries with high energy density.

  20. Structural modulation of lithium metal-electrolyte interface with three-dimensional metallic interlayer for high-performance lithium metal batteries

    Science.gov (United States)

    Lee, Hongkyung; Song, Jongchan; Kim, Yun-Jung; Park, Jung-Ki; Kim, Hee-Tak

    2016-08-01

    The use of lithium (Li) metal anodes has been reconsidered because of the necessity for a higher energy density in secondary batteries. However, Li metal anodes suffer from ‘dead’ Li formation and surface deactivation which consequently form a porous layer of redundant Li aggregates. In this work, a fibrous metal felt (FMF) as a three-dimensional conductive interlayer was introduced between the separator and the Li metal anode to improve the reversibility of the Li metal anode. The FMF can facilitate charge transfer in the porous layer, rendering it electrochemically more active. In addition, the FMF acted as a robust scaffold to accommodate Li deposits compactly in its interstitial sites. The FMF-integrated Li metal (FMF/Li) electrode operated with a small polarisation even at a current density of 10 mA cm-2, and it exhibited a seven times longer cycle-life than that of an FMF-free Li electrode in a symmetric cell configuration. A Li metal battery (LMB) using the FMF/Li electrode and a LiFePO4 electrode exhibited a two-fold increase in cycling stability compared with that of a bare Li metal electrode, demonstrating the practical effectiveness of this approach for high performance LMBs.

  1. Janus Separator of Polypropylene-Supported Cellular Graphene Framework for Sulfur Cathodes with High Utilization in Lithium-Sulfur Batteries.

    Science.gov (United States)

    Peng, Hong-Jie; Wang, Dai-Wei; Huang, Jia-Qi; Cheng, Xin-Bing; Yuan, Zhe; Wei, Fei; Zhang, Qiang

    2016-01-01

    Owing to the conversion chemistry of the sulfur cathode, the lithium-sulfur (Li-S) batteries exhibit high theoretical energy density. However, the intrinsic mobile redox centers during the sulfur/Li2S-to-lithium polysulfides solid-to-liquid phase transition induce low sulfur utilization and poor cycling life. Herein, the Janus separator of mesoporous cellular graphene framework (CGF)/polypropylene membrane to promote the utilization of sulfur cathode is introduced. The porous polypropylene membrane serves as an insulating substrate in contact with lithium anode while CGFs that possess high electrical conductivity of 100 S cm(-1), a large mesopore volume of 3.1 cm(3) g(-1), and a huge surface area of 2120 m(2) g(-1) are adhered on cathode side to reactivate the shuttling-back polysulfides and to preserve the ion channels. Therefore, the Li-S cell with the "two-face" CGF Janus separator exhibit a high initial capacity of 1109 mAh g(-1) and superior capacity preserved upon 800 mAh g(-1) after 250 cycles at 0.2 C, which is 40% higher on sulfur utilization efficiency than the corresponding results with routine polypropylene separators. There are significant improvements on capacity as well as electrochemical kinetics. A very high areal capacity of 5.5 mAh cm(-2) combined with high sulfur content of 80% and areal loading amount of 5.3 mg cm(-2) is achieved for such advanced configuration. The negative impact of shuttle mechanism on lowering the utilization of sulfur and overall energy density of a Li-S battery is well eliminated by applying CGF separators. Consequently, employing carbonaceous materials as Janus face of separators enlightens new opportunities for improving the utilization of active materials and energy density of devices that involve complex phase evolution and conversion electrochemistry.

  2. Calculation of the radionuclides in PWR spent fuel samples for SFR experiment planning.

    Energy Technology Data Exchange (ETDEWEB)

    Naegeli, Robert Earl

    2004-06-01

    This report documents the calculation of radionuclide content in the pressurized water reactor (PWR) spent fuel samples planned for use in the Spent Fuel Ratio (SPR) Experiments at Sandia National Laboratories, Albuquerque, New Mexico (SNL) to aid in experiment planning. The calculation methods using the ORIGEN2 and ORIGEN-ARP computer codes and the input modeling of the planned PWR spent fuel from the H. B. Robinson and the Surry nuclear power plants are discussed. The safety hazards for the calculated nuclide inventories in the spent fuel samples are characterized by the potential airborne dose and by the portion of the nuclear facility hazard category 2 and 3 thresholds that the experiment samples would present. In addition, the gamma ray photon energy source for the nuclide inventories is tabulated to facilitate subsequent calculation of the direct and shielded dose rates expected from the samples. The relative hazards of the high burnup 72 gigawatt-day per metric ton of uranium (GWd/MTU) spent fuel from H. B. Robinson and the medium burnup 36 GWd/MTU spent fuel from Surry are compared against a parametric calculation of various fuel burnups to assess the potential for higher hazard PWR fuel samples.

  3. Insights into the inner structure of high-nickel agglomerate as high-performance lithium-ion cathodes

    Science.gov (United States)

    Yang, Cheng-Kai; Qi, Li-Ya; Zuo, Zicheng; Wang, Ru-Na; Ye, Meng; Lu, Jing; Zhou, Heng-Hui

    2016-11-01

    In this paper, the intrinsic impact of inner structure features on the electrochemical performances of LiNi0.6Co0.2Mn0.2O2 cathodes is for the first time systematically investigated. Three different spherical Ni0.6Co0.2Mn0.2(OH)2 precursors are successfully synthesized by controlling pH values and ammonia concentrations. Interestingly, via a further lithiation process, the final cathodes can gradually inherit the structural features, showing distinct particle arrangement and genetic orientation characteristics in the inner structures. Such a hereditary property can be well reined for customizing the grain-orientation, helping the growth of the inert crystal direction, reducing cation mixing and exposing the high active (100) or (010) lattice planes for lithiation/delithiation processes via an intrinsical way. The degree of grain-orientation of the primary particles turns out to be a critical factor in determining the long-term stability and power performances. Due to the reduced cation mixing degree and favorable lithium diffusion pathways, the ordered agglomerates with the grain growth along with [003] direction exhibit superior rate capability and good cycle stability.

  4. High Energy, Long Cycle Life Lithium-ion Batteries for PHEV Application

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Donghai [Pennsylvania State Univ., University Park, PA (United States); Manthiram, Arumugam [Univ. of Texas, Austin, TX (United States); Wang, Chao-Yang [EC Power LLC, State College, PA (United States); Liu, Gao [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); Zhang, Zhengcheng [Argonne National Lab. (ANL), Argonne, IL (United States)

    2017-05-15

    High-loading and high quality PSU Si anode has been optimized and fabricated. The electrochemical performance has been utilized. The PSU Si-graphite anode exhibits the mass loading of 5.8 mg/cm2, charge capacity of 850 mAh/ g and good cycling performance. This optimized electrode has been used for full-cell fabrication. The performance enhancement of Ni-rich materials can be achieved by a diversity of strategies. Higher Mn content and a small amount of Al doping can improve the electrochemical performance by suppressing interfacial side reactions with electrolytes, thus greatly benefiting the cyclability of the samples. Also, surface coatings of Li-rich materials and AlF3 are able to improve the performance stability of Ni-rich cathodes. One kilogram of optimized concentration-gradient LiNi0.76Co0.10Mn0.14O2 (CG) with careful control of composition, morphology and electrochemical performance was delivered to our collaborators. The sample achieved an initial specific capacity close to 190 mA h g-1 at C/10 rate and 180 mA h g-1 at C/3 rate as well as good cyclability in pouch full cells with a 4.4 V upper cut-off voltage at room temperature. Electrolyte additive with Si-N skeleton forms a less resistant SEI on the surface of silicon anode (from PSU) as evidenced by the evolution of the impedance at various lithiation/de-lithiation stages and the cycling data The prelithiation result demonstrates a solution processing method to achieve large area, uniform SLMP coating on well-made anode surface for the prelithiation of lithium-ion batteries. The prelithiation effect with this method is applied both in graphite half cells, graphite/NMC full cells, SiO half cells, SiO/NMC full cells, Si-Graphite half cells and Si-Graphite/NMC full cells with improvements in cycle performance and higher first cycle coulombic efficiency than their corresponding cells without SLMP prelithiation. As to the full

  5. Ternary CNTs@TiO2/CoO Nanotube Composites: Improved Anode Materials for High Performance Lithium Ion Batteries

    Directory of Open Access Journals (Sweden)

    Mahmoud Madian

    2017-06-01

    Full Text Available TiO2 nanotubes (NTs synthesized by electrochemical anodization are discussed as very promising anodes for lithium ion batteries, owing to their high structural stability, high surface area, safety, and low production cost. However, their poor electronic conductivity and low Li+ ion diffusivity are the main drawbacks that prevent them from achieving high electrochemical performance. Herein, we report the fabrication of a novel ternary carbon nanotubes (CNTs@TiO2/CoO nanotubes composite by a two-step synthesis method. The preparation includes an initial anodic fabrication of well-ordered TiO2/CoO NTs from a Ti-Co alloy, followed by growing of CNTs horizontally on the top of the oxide films using a simple spray pyrolysis technique. The unique 1D structure of such a hybrid nanostructure with the inclusion of CNTs demonstrates significantly enhanced areal capacity and rate performances compared to pure TiO2 and TiO2/CoO NTs, without CNTs tested under identical conditions. The findings reveal that CNTs provide a highly conductive network that improves Li+ ion diffusivity, promoting a strongly favored lithium insertion into the TiO2/CoO NT framework, and hence resulting in high capacity and an extremely reproducible high rate capability.

  6. Nitrogen-doped 3D macroporous graphene frameworks as anode for high performance lithium-ion batteries

    Science.gov (United States)

    Liu, Xiaowu; Wu, Ying; Yang, Zhenzhong; Pan, Fusen; Zhong, Xiongwu; Wang, Jiaqing; Gu, Lin; Yu, Yan

    2015-10-01

    Nitrogen-doped 3D graphene frameworks (N-3D GFs) were synthesized by a facile two-step method: Polystyrene (PS) encapsulated in graphene oxide (GO) composites (denoted as PS@GO) are first synthesized, followed by a post-thermal annealing in ammonia step to get N-doped 3D GFs. The resulting N-3D GFs inherit the advantages of graphene, which possesses high electrical conductivity and high specific surface area. Furthermore, the well-defined 3D interconnected structure can facilitate the access of the electrolyte to the electrode surface, thus shortening the diffusion length of both Li+/e-, keeping the overall electrode highly conductive and active in lithium storage. Simultaneously, the in-situ formation of pyridinic N and pyrrolic N in 3D GFs provide high electronic conductivity and structure stability for lithium storage. The designed N-3D GFs electrode delivers a high specific capacity of 1094 mAhg-1 after 100 cycles at 200 mAg-1 and superior rate capability (691 mAhg-1 after 500 cycles at 1000 mAg-1) when used as anode for LIBs. We believe that such an inherently inexpensive, scalable, facile method can significantly increase the feasibility of building high performance energy storage system.

  7. Ternary CNTs@TiO₂/CoO Nanotube Composites: Improved Anode Materials for High Performance Lithium Ion Batteries.

    Science.gov (United States)

    Madian, Mahmoud; Ummethala, Raghunandan; Naga, Ahmed Osama Abo El; Ismail, Nahla; Rümmeli, Mark Hermann; Eychmüller, Alexander; Giebeler, Lars

    2017-06-20

    TiO₂ nanotubes (NTs) synthesized by electrochemical anodization are discussed as very promising anodes for lithium ion batteries, owing to their high structural stability, high surface area, safety, and low production cost. However, their poor electronic conductivity and low Li⁺ ion diffusivity are the main drawbacks that prevent them from achieving high electrochemical performance. Herein, we report the fabrication of a novel ternary carbon nanotubes (CNTs)@TiO₂/CoO nanotubes composite by a two-step synthesis method. The preparation includes an initial anodic fabrication of well-ordered TiO₂/CoO NTs from a Ti-Co alloy, followed by growing of CNTs horizontally on the top of the oxide films using a simple spray pyrolysis technique. The unique 1D structure of such a hybrid nanostructure with the inclusion of CNTs demonstrates significantly enhanced areal capacity and rate performances compared to pure TiO₂ and TiO₂/CoO NTs, without CNTs tested under identical conditions. The findings reveal that CNTs provide a highly conductive network that improves Li⁺ ion diffusivity, promoting a strongly favored lithium insertion into the TiO₂/CoO NT framework, and hence resulting in high capacity and an extremely reproducible high rate capability.

  8. Flakelike LiCoO2 with Exposed {010} Facets As a Stable Cathode Material for Highly Reversible Lithium Storage.

    Science.gov (United States)

    Wu, Naiteng; Zhang, Yun; Guo, Yi; Liu, Shengjie; Liu, Heng; Wu, Hao

    2016-02-03

    A thick and dense flakelike LiCoO2 with exposed {010} active facets is synthesized using Co(OH)2 nanoflake as a self-sacrificial template obtained from a simple coprecipitation method, and served as a cathode material for lithium ion batteries. When operated at a high cutoff voltage up to 4.5 V, the resultant LiCoO2 exhibits an outstanding rate capability, delivering a reversible discharge capacity as high as 179, 176, 168, 116, and 96 mA h g(-1) at 25 °C under the current rate of 0.1, 0.5, 1, 5, and 10 C, respectively. When charge/discharge cycling at 55 °C, a high specific capacity of 148 mA h g(-1) (∼88% retention) can be retained after 100 cycles under 1 C, demonstrating excellent cycling and thermal stability. Besides, the flakelike LiCoO2 also shows an impressive low-temperature electrochemical activity with specific capacities of 175 (0.1 C) and 154 mA h g(-1) (1 C) at -10 °C, being the highest ever reported for a subzero-temperature lithium storage capability, as well as 52% capacity retention even after 80 cycles under 1 C. Such superior high-voltage electrochemical performances of the flakelike LiCoO2 operated at a wide temperature range are mainly attributed to its unique hierarchical structure with specifically exposed facets. The exposed {010} active facets provide a preferential crystallographic orientation for Li-ion migration, while the micrometer-sized secondary particles agglomerated by submicron primary LiCoO2 flakes endow the electrode with better structural integrity, both of which ensure the LiCoO2 cathode to manifest remarkably enhanced reversible lithium storage properties.

  9. High reversible capacity of SnO{sub 2}/graphene nanocomposite as an anode material for lithium-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Lian Peichao [School of Chemistry and Chemical Engineering, South China University of Technology, No. 381 Wushan Road, Guangzhou 510640 (China); Zhu Xuefeng [State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023 (China); Liang Shuzhao; Li Zhong [School of Chemistry and Chemical Engineering, South China University of Technology, No. 381 Wushan Road, Guangzhou 510640 (China); Yang Weishen [State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023 (China); Wang Haihui, E-mail: hhwang@scut.edu.c [School of Chemistry and Chemical Engineering, South China University of Technology, No. 381 Wushan Road, Guangzhou 510640 (China)

    2011-04-30

    Highlights: {yields} Gas-liquid interfacial reaction was used to prepare SnO{sub 2}/graphene nanocomposite. {yields} SnO{sub 2}/graphene nanocomposite as an anode for lithium-ion batteries. {yields} It exhibited high reversible specific capacity and excellent cycle capability. {yields} Graphene sheets can improve the cycling performance and reverible capacity of SnO{sub 2}. - Abstract: A gas-liquid interfacial synthesis approach has been developed to prepare SnO{sub 2}/graphene nanocomposite. The as-prepared nanocomposite was characterized by X-ray diffraction, field emission scanning electron microscopy, transmission electron microscopy, and Brunauer-Emmett-Teller measurements. Field emission scanning electron microscopy and transmission electron microscopy observation revealed the homogeneous distribution of SnO{sub 2} nanoparticles (2-6 nm in size) on graphene matrix. The electrochemical performances were evaluated by using coin-type cells versus metallic lithium. The SnO{sub 2}/graphene nanocomposite prepared by the gas-liquid interface reaction exhibits a high reversible specific capacity of 1304 mAh g{sup -1} at a current density of 100 mA g{sup -1} and excellent rate capability, even at a high current density of 1000 mA g{sup -1}, the reversible capacity was still as high as 748 mAh g{sup -1}. The electrochemical test results show that the SnO{sub 2}/graphene nanocomposite prepared by the gas-liquid interfacial synthesis approach is a promising anode material for lithium-ion batteries.

  10. Lithium Poisoning

    DEFF Research Database (Denmark)

    Baird-Gunning, Jonathan; Lea-Henry, Tom; Hoegberg, Lotte C G

    2017-01-01

    is required. The cause of lithium poisoning influences treatment and 3 patterns are described: acute, acute-on-chronic, and chronic. Chronic poisoning is the most common etiology, is usually unintentional, and results from lithium intake exceeding elimination. This is most commonly due to impaired kidney...... function caused by volume depletion from lithium-induced nephrogenic diabetes insipidus or intercurrent illnesses and is also drug-induced. Lithium poisoning can affect multiple organs; however, the primary site of toxicity is the central nervous system and clinical manifestations vary from asymptomatic...... supratherapeutic drug concentrations to clinical toxicity such as confusion, ataxia, or seizures. Lithium poisoning has a low mortality rate; however, chronic lithium poisoning can require a prolonged hospital length of stay from impaired mobility and cognition and associated nosocomial complications. Persistent...

  11. Growth and decomposition of Lithium and Lithium hydride on Nickel

    DEFF Research Database (Denmark)

    Engbæk, Jakob; Nielsen, Gunver; Nielsen, Jane Hvolbæk

    2006-01-01

    In this paper we have investigated the deposition, structure and decomposition of lithium and lithium-hydride films on a nickel substrate. Using surface sensitive techniques it was possible to quantify the deposited Li amount, and to optimize the deposition procedure for synthesizing lithium......-hydride films. By only making thin films of LiH it is possible to study the stability of these hydride layers and compare it directly with the stability of pure Li without having any transport phenomena or adsorbed oxygen to obscure the results. The desorption of metallic lithium takes place at a lower...... temperature than the decomposition of the lithium-hydride, confirming the high stability and sintering problems of lithium-hydride making the storage potential a challenge. (c) 2006 Elsevier B.V. All rights reserved....

  12. Lithium-Associated Kidney Microcysts

    OpenAIRE

    Jennifer Tuazon; David Casalino; Ehteshamuddin Syed; Daniel Batlle

    2008-01-01

    Long-term lithium therapy is associated with impairment in concentrating ability and, occasionally, progression to advanced chronic kidney disease from tubulointerstitial nephropathy. Biopsy findings in patients with lithium-induced chronic tubulointerstitial nephropathy include tubular atrophy and interstitial fibrosis interspersed with tubular cysts and dilatations. Recent studies have shown that cysts are seen in 33––62.5% of the patients undergoing lithium therapy. MR imaging is highly ca...

  13. The characterization of secondary lithium-ion battery degradation when operating complex, ultra-high power pulsed loads

    Science.gov (United States)

    Wong, Derek N.

    The US Navy is actively developing all electric fleets, raising serious questions about what is required of onboard power supplies in order to properly power the ship's electrical systems. This is especially relevant when choosing a viable power source to drive high power propulsion and electric weapon systems in addition to the conventional loads deployed aboard these types of vessels. Especially when high pulsed power loads are supplied, the issue of maintaining power quality becomes important and increasingly complex. Conventionally, a vessel's electrical power is generated using gas turbine or diesel driven motor-generator sets that are very inefficient when they are used outside of their most efficient load condition. What this means is that if the generator is not being utilized continuously at its most efficient load capacity, the quality of the output power may also be effected and fall outside of the acceptable power quality limits imposed through military standards. As a solution to this potential problem, the Navy has proposed using electrochemical storage devices since they are able to buffer conventional generators when the load is operating below the generator's most efficient power level or able to efficiently augment a generator when the load is operating in excess of the generator's most efficient power rating. Specifically, the US Navy is interested in using commercial off-the-shelf (COTS) lithium-ion batteries within an intelligently controlled energy storage module that could act as either a prime power supply for on-board pulsed power systems or as a backup generator to other shipboard power systems. Due to the unique load profile of high-rate pulsed power systems, the implementation of lithium-ion batteries within these complex systems requires them to be operated at very high rates and the effects these things have on cell degradation has been an area of focus. There is very little published research into the effects that high power transient

  14. Conceptual study of advanced PWR core design. Development of advanced PWR core neutronics analysis system

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Chang Hyo; Kim, Seung Cho; Kim, Taek Kyum; Cho, Jin Young; Lee, Hyun Cheol; Lee, Jung Hun; Jung, Gu Young [Seoul National University, Seoul (Korea, Republic of)

    1995-08-01

    The neutronics design system of the advanced PWR consists of (i) hexagonal cell and fuel assembly code for generation of homogenized few-group cross sections and (ii) global core neutronics analysis code for computations of steady-state pin-wise or assembly-wise core power distribution, core reactivity with fuel burnup, control rod worth and reactivity coefficients, transient core power, etc.. The major research target of the first year is to establish the numerical method and solution of multi-group diffusion equations for neutronics code development. Specifically, the following studies are planned; (i) Formulation of various numerical methods such as finite element method(FEM), analytical nodal method(ANM), analytic function expansion nodal(AFEN) method, polynomial expansion nodal(PEN) method that can be applicable for the hexagonal core geometry. (ii) Comparative evaluation of the numerical effectiveness of these methods based on numerical solutions to various hexagonal core neutronics benchmark problems. Results are follows: (i) Formulation of numerical solutions to multi-group diffusion equations based on numerical methods. (ii) Numerical computations by above methods for the hexagonal neutronics benchmark problems such as -VVER-1000 Problem Without Reflector -VVER-440 Problem I With Reflector -Modified IAEA PWR Problem Without Reflector -Modified IAEA PWR Problem With Reflector -ANL Large Heavy Water Reactor Problem -Small HTGR Problem -VVER-440 Problem II With Reactor (iii) Comparative evaluation on the numerical effectiveness of various numerical methods. (iv) Development of HEXFEM code, a multi-dimensional hexagonal core neutronics analysis code based on FEM. In the target year of this research, the spatial neutronics analysis code for hexagonal core geometry(called NEMSNAP-H temporarily) will be completed. Combination of NEMSNAP-H with hexagonal cell and assembly code will then equip us with hexagonal core neutronics design system. (Abstract Truncated)

  15. Hollow-Cuboid Li3VO4/C as High-Performance Anodes for Lithium-Ion Batteries.

    Science.gov (United States)

    Zhang, Changkun; Liu, Chaofeng; Nan, Xihui; Song, Huanqiao; Liu, Yaguang; Zhang, Cuiping; Cao, Guozhong

    2016-01-13

    Li3VO4 has been demonstrated to be a promising anode material for lithium-ion batteries with a low, safe voltage and large capacity. However, its poor electronic conductivity hinders its practical application particularly at a high rate. This work reports that Li3VO4 coated with carbon was synthesized by a one-pot, two-step method with F127 ((PEO)100-(PPO)65-(PEO)100) as both template and carbon source, yielding a microcuboid structure. The resulting Li3VO4/C cuboid shows a stable capacity of 415 mAh g(-1) at 0.5 C and excellent capacity stability at high rates (e.g., 92% capacity retention after 1000 cycles at 10 C = 4 A g(-1)). The lithiation/delithiation process of Li3VO4/C was studied by ex situ X-ray diffraction and Raman spectroscopy, which confirmed that Li3VO4/C underwent a reversible intercalation reaction during discharge/charge processes. The excellent electrochemical performance is attributed largely to the unique microhollow structure. The voids inside hollow structure can not only provide more space to accommodate volume change during discharge/charge processes but also allow the lithium ions insertion and extraction from both outside and inside the hollow structure with a much larger surface area or more reaction sites and shorten the lithium ions diffusion distance, which leads to smaller overpotential and faster reaction kinetics. Carbon derived from F127 through pyrolysis coats Li3VO4 conformably and thus offers good electrical conduction. The results in this work provide convincing evidence that the significant potential of hollow-cuboid Li3VO4/C for high-power batteries.

  16. New lithium gas sorbents

    Energy Technology Data Exchange (ETDEWEB)

    Chuntonov, K. [Nanoshell Materials R and D GmbH, Primoschgasse 3, 9020 Klagenfurt (Austria)], E-mail: k.chuntonov@nanoshell.at; Setina, J. [Institute of Metals and Technology, 1000 Ljubljana (Slovenia)

    2008-05-08

    Solid solutions of lithium in Ag and Cu in the form of balls, wires, or strips are convenient sources for depositing lithium films as getters on the walls of vacuum vessels. Measurement of the O{sub 2}, CO and CO{sub 2} sorption characteristics have shown that these films - e.g. those generated electrothermally from Ag/Li solid solutions - excel the best getters of the Ba-film type or the high porosity getters based on Ti, V and Zr alloys. It has been found that tight lithium films passivate as a sorption depth of approximately 100 A is reached. Methods for further improvement of the sorption behavior of lithium coatings are discussed.

  17. High efficiency electrotransformation of Lactococcus lactis spp. lactis cells pretreated with lithium acetate and dithiothreitol

    Directory of Open Access Journals (Sweden)

    Filioussis George

    2007-03-01

    Full Text Available Abstract Background A goal for the food industry has always been to improve strains of Lactococcus lactis and stabilize beneficial traits. Genetic engineering is used extensively for manipulating this lactic acid bacterium, while electropolation is the most widely used technique for introducing foreign DNA into cells. The efficiency of electrotransformation depends on the level of electropermealization and pretreatment with chemicals which alter cell wall permeability, resulting in improved transformation efficiencies is rather common practice in bacteria as in yeasts and fungi. In the present study, treatment with lithium acetate (LiAc and dithiothreitol (DTT in various combinations was applied to L. lactis spp. lactis cells of the early-log phase prior to electroporation with plasmid pTRKH3 (a 7.8 kb shuttle vector, suitable for cloning into L. lactis. Two strains of L. lactis spp. lactis were used, L. lactis spp. lactis LM0230 and ATCC 11454. To the best of our knowledge these agents have never been used before with L. lactis or other bacteria. Results Electrotransformation efficiencies of up to 105 transformants per μg DNA have been reported in the literature for L. lactis spp.lactis LM0230. We report here that treatment with LiAc and DDT before electroporation increased transformation efficiency to 225 ± 52.5 × 107 transformants per μg DNA, while with untreated cells or treated with LiAc alone transformation efficiency approximated 1.2 ± 0.5 × 105 transformants per μg DNA. Results of the same trend were obtained with L. lactis ATCC 11454, although transformation efficiency of this strain was significantly lower. No difference was found in the survival rate of pretreated cells after electroporation. Transformation efficiency was found to vary directly with cell density and that of 1010 cells/ml resulted in the highest efficiencies. Following electrotransformation of pretreated cells with LiAc and DDT, pTRKH3 stability was examined

  18. Highly conductive bridges between graphite spheres to improve the cycle performance of a graphite anode in lithium-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Hongyu [IM and T Ltd., Advanced Research Center, Saga University, Yoga-machi 1341, Saga 840-0047 (Japan); Umeno, Tatsuo; Mizuma, Koutarou [Research Center, Mitsui Mining Co. Ltd., Hibiki-machi 1-3, Wakamatsu-ku, Kitakyushu 808-0021 (Japan); Yoshio, Masaki [Advanced Research Center, Saga University, Yoga-machi 1341, Saga 840-0047 (Japan)

    2008-01-10

    Spherical carbon-coated natural graphite (SCCNG) is a promising anode material for lithium-ion batteries, but the smooth surface of graphite spheres is difficult to wet with an aqueous binder solution, and lacks electrical contacts. As a result, the cycle performance of such a graphite anode material is not satisfactory. An effective method has been introduced to tightly connect adjacent SCCNG particles by a highly conductive binder, viz. acetylene black bridges. The effect of the conductive bridges on the cyclability of SCCNG electrode has been investigated. (author)

  19. Enhanced Reaction Kinetics and Structure Integrity of Ni/SnO2 Nanocluster toward High-Performance Lithium Storage.

    Science.gov (United States)

    Jiang, Yinzhu; Li, Yong; Zhou, Peng; Yu, Shenglan; Sun, Wenping; Dou, Shixue

    2015-12-09

    SnO2 is regarded as one of the most promising anodes via conversion-alloying mechanism for advanced lithium ion batteries. However, the sluggish conversion reaction severely degrades the reversible capacity, Coulombic efficiency and rate capability. In this paper, through constructing porous Ni/SnO2 composite electrode composed of homogeneously distributed SnO2 and Ni nanoparticles, the reaction kinetics of SnO2 is greatly enhanced, leading to full conversion reaction, superior cycling stability and improved rate capability. The uniformly distributed Ni nanoparticles provide a fast charge transport pathway for electrochemical reactions, and restrict the direct contact and aggregation of SnO2 nanoparticles during cycling. In the meantime, the void space among the nanoclusters increases the contact area between the electrolyte and active materials, and accommodates the huge volume change during cycling as well. The Ni/SnO2 composite electrode possesses a high reversible capacity of 820.5 mAh g(-1) at 1 A g(-1) up to 100 cycles. More impressively, large capacity of 841.9, 806.6, and 770.7 mAh g(-1) can still be maintained at high current densities of 2, 5, and 10 A g(-1) respectively. The results demonstrate that Ni/SnO2 is a high-performance anode for advanced lithium-ion batteries with high specific capacity, excellent rate capability, and cycling stability.

  20. Sandwich-Structured Graphene-Fe3O4@Carbon Nanocomposites for High-Performance Lithium-Ion Batteries.

    Science.gov (United States)

    Zhao, Li; Gao, Miaomiao; Yue, Wenbo; Jiang, Yang; Wang, Yuan; Ren, Yu; Hu, Fengqin

    2015-05-13

    Advanced anode materials for high power and high energy lithium-ion batteries have attracted great interest due to the increasing demand for energy conversion and storage devices. Metal oxides (e.g., Fe3O4) usually possess high theoretical capacities, but poor electrochemical performances owing to their severe volume change and poor electronic conductivity during cycles. In this work, we develop a self-assembly approach for the synthesis of sandwich-structured graphene-Fe3O4@carbon composite, in which Fe3O4 nanoparticles with carbon layers are immobilized between the layers of graphene nanosheets. Compared to Fe3O4@carbon and bulk Fe3O4, graphene-Fe3O4@carbon composite shows superior electrochemical performance, including higher reversible capacity, better cycle and rate performances, which may be attributed to the sandwich structure of the composite, the nanosized Fe3O4, and the carbon layers on the surface of Fe3O4. Moreover, compared to the reported graphene-Fe3O4 composite, the particle size of Fe3O4 is controllable and the content of Fe3O4 in this composite can be arbitrarily adjusted for optimal performance. This novel synthesis strategy may be employed in other sandwich-structured nanocomposites design for high-performance lithium-ion batteries and other electrochemical devices.

  1. Hierarchical Porous Nickel Cobaltate Nanoneedle Arrays as Flexible Carbon-Protected Cathodes for High-Performance Lithium-Oxygen Batteries.

    Science.gov (United States)

    Xue, Hairong; Wu, Shichao; Tang, Jing; Gong, Hao; He, Ping; He, Jianping; Zhou, Haoshen

    2016-04-06

    Rechargeable lithium-oxygen (Li-O2) batteries are consequently considered to be an attractive energy storage technology because of the high theoretical energy densities. Here, an effective binder-free cathode with high capacity for Li-O2 batteries, needle-like mesoporous NiCo2O4 nanowire arrays uniformly coated on the flexible carbon textile have been in situ fabricated via a facile hydrothermal process followed by low temperature calcination. Because of the material and structural features, the needle-like NiCo2O4 nanowire arrays (NCONWAs) served as a binder-free cathode exhibits high specific capacity (4221 mAh g(-1)), excellent rate capability, and outstanding cycling stability (200 cycles). This cathode based on nonprecious mesoporous metal oxides nanowire arrays has large open spaces and high surface area, providing numerous catalytically active sites and effective transmission pathways for lithium ion and oxygen, and promises the abundant Li2O2 storage. The fast electron transport by directly anchoring on the substrate ensures fast electrochemical reaction process involved with the every nanowire. Furthermore, a bendable Li-O2 battery assembled by using the flexible NCONWAs as the cathode, can be able to light an LED and shows good rate capability and cyclic stability.

  2. Conductive Polymer Binder for High-Tap-Density Nanosilicon Material for Lithium-Ion Battery Negative Electrode Application.

    Science.gov (United States)

    Zhao, Hui; Wei, Yang; Qiao, Ruimin; Zhu, Chenhui; Zheng, Ziyan; Ling, Min; Jia, Zhe; Bai, Ying; Fu, Yanbao; Lei, Jinglei; Song, Xiangyun; Battaglia, Vincent S; Yang, Wanli; Messersmith, Phillip B; Liu, Gao

    2015-12-09

    High-tap-density silicon nanomaterials are highly desirable as anodes for lithium ion batteries, due to their small surface area and minimum first-cycle loss. However, this material poses formidable challenges to polymeric binder design. Binders adhere on to the small surface area to sustain the drastic volume changes during cycling; also the low porosities and small pore size resulting from this material are detrimental to lithium ion transport. This study introduces a new binder, poly(1-pyrenemethyl methacrylate-co-methacrylic acid) (PPyMAA), for a high-tap-density nanosilicon electrode cycled in a stable manner with a first cycle efficiency of 82%-a value that is further improved to 87% when combined with graphite material. Incorporating the MAA acid functionalities does not change the lowest unoccupied molecular orbital (LUMO) features or lower the adhesion performance of the PPy homopolymer. Our single-molecule force microscopy measurement of PPyMAA reveals similar adhesion strength between polymer binder and anode surface when compared with conventional polymer such as homopolyacrylic acid (PAA), while being electronically conductive. The combined conductivity and adhesion afforded by the MAA and pyrene copolymer results in good cycling performance for the high-tap-density Si electrode.

  3. Lithium iron phosphate battery electrode integrity following high speed pulsed laser cutting

    Science.gov (United States)

    Lutey, Adrian H. A.; Fiorini, Maurizio; Fortunato, Alessandro; Carmignato, Simone

    2015-05-01

    Laser exposures are performed on lithium iron phosphate battery electrodes at with process parameters based on those leading to the smallest heat affected zone for low power laser exposure at . Scanning electron microscopy and Raman analysis are performed along the resulting cut edges to characterize macroscopic, chemical and microstructural changes resulting from laser exposure. The increase in velocity with respect to previous studies is found to limit macroscopic changes to areas directly exposed to the laser beam and greatly suppress or completely eliminate microstructural and chemical changes resulting from thermal conduction effects in the metallic conductor layers. These results confirm laser technology as a viable, more flexible solution to mechanical blanking devices for the cutting of lithium iron phosphate battery electrode films.

  4. High-G Verification of Lithium-Polymer (Li-Po) Pouch Cells

    Science.gov (United States)

    2016-05-19

    options are available with different sizes , capacities, and charge/discharge rates. Lithium batteries are one available option that comes in many form...telemetry systems, it is the size constraint requirements that drives the choice of battery . The batteries investigated in this study that meet the...systems’ power and size requirements are the Hyperion G3CX 240 mAH and Power Stream GMB052025 (also known as GM052025). Details of the batteries are

  5. Nanoconfinement of LiBH4 for High Ionic Conductivity in Lithium Ion Batteries

    DEFF Research Database (Denmark)

    Lefevr, Jessica Emilia Avlina; Das, Supti; Blanchard, Didier

    2016-01-01

    Efficient energy conversion and storage is crucial for development of systems based on renewable energy sources. For electricity storage, Li-ion batteries are commonly used in electronics devices but require many improvements to obtain longer life-time and higher energy densities. The current use...... of organic liquids and gels electrolytes limits these improvements because of lithium dendrites formation, reducing the lifetime of the battery and which can possibly be hazardous due to risks of short circuits....

  6. Difficulties Encountered in Stabilization of Lithium Serum Levels in a High Blood Pressure Patient

    Directory of Open Access Journals (Sweden)

    Carlos Vieira

    2014-10-01

    Full Text Available Based on the clinical case of a female in-patient of the Psychiatric Departement of the Fernando Fonseca Hospital, who was admitted due to bipolar disorder relapse and to whom arterial hypertension was diagnosed during her stay in the ward, the authors review the interactions between mood stabilizer therapy with lithium and anti-hypertensive therapy (emphasizing on angiotensin-converting enzyme – ACE – inhibitors and diuretics, both necessary to her clinical stabilization.

  7. Elastic and wearable wire-shaped lithium-ion battery with high electrochemical performance.

    Science.gov (United States)

    Ren, Jing; Zhang, Ye; Bai, Wenyu; Chen, Xuli; Zhang, Zhitao; Fang, Xin; Weng, Wei; Wang, Yonggang; Peng, Huisheng

    2014-07-21

    A stretchable wire-shaped lithium-ion battery is produced from two aligned multi-walled carbon nanotube/lithium oxide composite yarns as the anode and cathode without extra current collectors and binders. The two composite yarns can be well paired to obtain a safe battery with superior electrochemical properties, such as energy densities of 27 Wh kg(-1) or 17.7 mWh cm(-3) and power densities of 880 W kg(-1) or 0.56 W cm(-3), which are an order of magnitude higher than the densities reported for lithium thin-film batteries. These wire-shaped batteries are flexible and light, and 97 % of their capacity was maintained after 1000 bending cycles. They are also very elastic as they are based on a modified spring structure, and 84 % of the capacity was maintained after stretching for 200 cycles at a strain of 100 %. Furthermore, these novel wire-shaped batteries have been woven into lightweight, flexible, and stretchable battery textiles, which reveals possible large-scale applications.

  8. Erosion of lithium coatings on TZM molybdenum and graphite during high-flux plasma bombardment

    Energy Technology Data Exchange (ETDEWEB)

    Abrams, T., E-mail: tabrams@pppl.gov [Princeton Plasma Physics Laboratory, Princeton, NJ 08543 (United States); Jaworski, M.A.; Kaita, R.; Stotler, D.P. [Princeton Plasma Physics Laboratory, Princeton, NJ 08543 (United States); De Temmerman, G.; Morgan, T.W.; Berg, M.A. van den; Meiden, H.J. van der [FOM Institute DIFFER – Dutch Institute For Fundamental Energy Research, Trilateral Euregio Cluster, Associate EURATOM-FOM, BL-3430 BE Nieuwegein (Netherlands)

    2014-12-15

    Highlights: • A formula for temperature-dependent lithium sputtering and evaporation is proposed. • This formula was tested using the Magnum-PSI linear plasma device. • Lithium-coated TZM molybdenum and graphite samples were exposed to plasmas. • Measured Li erosion rates are significantly lower than the formula predicts. • Evidence of lithium diffusion into graphite substrates was also observed. - Abstract: The rate at which Li films will erode under plasma bombardment in the NSTX-U divertor is currently unknown. It is important to characterize this erosion rate so that the coatings can be replenished before they are completely depleted. An empirical formula for the Li erosion rate as a function of deuterium ion flux, incident ion energy, and Li temperature was developed based on existing theoretical and experimental work. These predictions were tested on the Magnum-PSI linear plasma device capable of ion fluxes >10{sup 24} m{sup −2} s{sup −1}, ion energies of 20 eV and Li temperatures >800 °C. Li-coated graphite and TZM molybdenum samples were exposed to a series of plasma pulses during which neutral Li radiation was measured with a fast camera. The total Li erosion rate was inferred from measurements of Li-I emission. The measured erosion rates are significantly lower than the predictions of the empirical formula. Strong evidence of fast Li diffusion into graphite substrates was also observed.

  9. Inorganic Glue Enabling High Performance of Silicon Particles as Lithium Ion Battery Anode

    KAUST Repository

    Cui, Li-Feng

    2011-01-01

    Silicon, as an alloy-type anode material, has recently attracted lots of attention because of its highest known Li+ storage capacity (4200 mAh/g). But lithium insertion into and extraction from silicon are accompanied by a huge volume change, up to 300, which induces a strong strain on silicon and causes pulverization and rapid capacity fading due to the loss of the electrical contact between part of silicon and current collector. Silicon nanostructures such as nanowires and nanotubes can overcome the pulverization problem, however these nano-engineered silicon anodes usually involve very expensive processes and have difficulty being applied in commercial lithium ion batteries. In this study, we report a novel method using amorphous silicon as inorganic glue replacing conventional polymer binder. This inorganic glue method can solve the loss of contact issue in conventional silicon particle anode and enables successful cycling of various sizes of silicon particles, both nano-particles and micron particles. With a limited capacity of 800 mAh/g, relatively large silicon micron-particles can be stably cycled over 200 cycles. The very cheap production of these silicon particle anodes makes our method promising and competitive in lithium ion battery industry. © 2011 The Electrochemical Society.

  10. Symposium on High Power, Ambient Temperature Lithium Batteries, 180th Meeting of the Electrochemical Society, Phoenix, AZ, Oct. 13-17, 1991, Proceedings

    Science.gov (United States)

    Clark, W. D. K. (Editor); Halpert, Gerald (Editor)

    1992-01-01

    Papers presented in these proceedings are on the state of the art in high-power lithium batteries, a design analysis of high-power Li-TiS2 battery, the performance and safety features of spiral wound lithium/thionyl chloride cells, the feasibility of a superhigh energy density battery of the Li/BrF3 electrochemical system, and an enhanced redox process of disulfide compounds and their application in high energy storage. Attention is also given to the structure and charge-discharge characteristics of mesophase-pitch based carbons, a study of carbons and graphites as anodes for lithium rechargeable cells, Li metal-free rechargeable Li(1+x)Mn2O4/carbon cells, and rechargeable lithium batteries using V6O13/V5O5 as the positive electrode material. Other papers discuss the electrochemical stability of organic electrolytes in contact with solid inorganic cathode materials, the electrochemical behavior of methyl formate solutions, and the interface between a solid polymer electrolyte and lithium anode.

  11. Three-dimensional SnO2/carbon on Cu foam for high-performance lithium ion battery anodes

    Science.gov (United States)

    Chen, Weimin; Maloney, Scott; Wang, Wenyong

    2016-10-01

    SnO2 is an attractive anode material for lithium-ion batteries (LIBs) due to its high theoretical specific capacity (1491 mAh g-1), low cost, and environmental benignity. The main challenges for SnO2 anodes are their low intrinsic conductivity and poor cycling stability associated with their large volume changes during the charge and discharge process. Here, we present a simple chemical vapor deposition method to fabricate three-dimensional SnO2/carbon on Cu foam electrodes for LIBs. Such a three-dimensional electrode combines multiple advantages, including a continuous electrically conductive network, short pathways for electron transport and ion diffusion, and porous space to allow for the volume expansion of SnO2 nanoparticles. With this anode, superior electrochemical performance is achieved with a high reversible specific capacity of 1171 mAh g-1 at a current density of 100 mA g-1. A stable cycling performance as well as an excellent rate capability is also achieved. These outstanding lithium-storage properties suggest the strategy is a reliable approach for fabricating high-performance LIB electrodes.

  12. Mn 3 O 4 −Graphene Hybrid as a High-Capacity Anode Material for Lithium Ion Batteries

    KAUST Repository

    Wang, Hailiang

    2010-10-13

    We developed two-step solution-phase reactions to form hybrid materials of Mn3O4 nanoparticles on reduced graphene oxide (RGO) sheets for lithium ion battery applications. Selective growth of Mn3O 4 nanoparticles on RGO sheets, in contrast to free particle growth in solution, allowed for the electrically insulating Mn3O4 nanoparticles to be wired up to a current collector through the underlying conducting graphene network. The Mn3O4 nanoparticles formed on RGO show a high specific capacity up to ∼900 mAh/g, near their theoretical capacity, with good rate capability and cycling stability, owing to the intimate interactions between the graphene substrates and the Mn 3O4 nanoparticles grown atop. The Mn3O 4/RGO hybrid could be a promising candidate material for a high-capacity, low-cost, and environmentally friendly anode for lithium ion batteries. Our growth-on-graphene approach should offer a new technique for the design and synthesis of battery electrodes based on highly insulating materials. © 2010 American Chemical Society.

  13. On-chip high-power porous silicon lithium ion batteries with stable capacity over 10000 cycles (Presentation Recording)

    Science.gov (United States)

    Westover, Andrew S.; Freudiger, Daniel; Gani, Zarif; Share, Keith; Oakes, Landon; Carter, Rachel E.; Pint, Cary L.

    2015-09-01

    We demonstrate the operation of a graphene-passivated on-chip porous silicon material as a high rate lithium ion battery anode with over 50x power density and 100x energy density improvement compared to identically prepared on-chip porous silicon supercapacitors. We demonstrate this Faradaic storage behavior to occur at fast charging rates (1-10 mA/cm2) where lithium locally intercalates into the nanoporous silicon, but not underlying bulk silicon material. This prevents the degradation and poor cycling performance that is commonly observed from deep storage in bulk silicon materials. As a result, this device exhibits cycling performance that exceeds 10,000 cycles with capacity above 0.1 mAh/cm2, without notable capacity fade. This work demonstrates a practical route toward high power, high energy, and long lifetime all-silicon on-chip storage systems relevant toward integration of energy storage into electronics, photovoltaics, and other silicon-based technology.

  14. Preparation of three-dimensional hybrid nanostructure-encapsulated sulfur cathode for high-rate lithium sulfur batteries

    Science.gov (United States)

    Xie, Jing; Yang, Juan; Zhou, Xiangyang; Zou, Youlan; Tang, Jingjing; Wang, Songcan; Chen, Feng

    2014-05-01

    A three-dimensional hybrid nanostructure incorporating the merits of the MWCNTs webs (MWCNTs-W) and the reduced graphene oxide (RGO) is designed to improve the high-rate cycling performance of the lithium-sulfur batteries. Owing to the excellent Li+ ion and electronic transport properties of the MWCNTs-W and the RGO, this unique structure can provide a three-dimensional conductive network and promote rapid charge-transfer reaction at the cathode. Furthermore, because of the rough surface and porous structure of the MWCNTs after activation with KOH, and the special adsorption ability of the RGO, the soluble polysulfide intermediates can be effectively trapped in the cathode. Therefore, when evaluating the electrochemical properties of the RGO@MWCNTs-W/S composite as the cathode material for lithium-sulfur batteries, it exhibits an excellent cyclical stability and high rate performance. In particular, even at an ultrahigh rate (5 C), a discharge capacity as high as 620 mAh g-1 is still retained for the RGO@MWCNTs-W/S composite with 68.93 wt% sulfur after 200 cycles, and the average coulombic efficiency is 96%.

  15. Study of Microstructure Change of Carbon Nanofibers as Binder-Free Anode for High-Performance Lithium-Ion Batteries.

    Science.gov (United States)

    Wang, Ting; Shi, Shaojun; Li, Yuhong; Zhao, Mengxi; Chang, Xiaofeng; Wu, Di; Wang, Haiying; Peng, Luming; Wang, Peng; Yang, Gang

    2016-12-07

    Flexible and binder-free film of N, O-doped carbon nanofibers (CNFs) is the ideal anode for high-energy-density batteries. Here, CNFs flexible films which the N, O dopant give defect in graphite structure results in high specific surface area more than 500 m(2) g(-1). A flexible film of CNF800 carbonized at 800 °C delivers initial capacities of 2000 and 755 mAh g(-1) at the current densities of 5 and 10 A g(-1), respectively. After 500 cycles, CNF800 remains the capacities of 1251, 865, 702, and 305 mAh g(-1) at 0.5, 1, 5, and 10 A g(-1), respectively. The microstructures of CNFs under various state of charge are studied by HRTEM, XPS, (13)C NMR, and so forth. The lithiation/delithiation mainly happens to the interlayer of graphite domain of CNFs. The dopants of nitrogen and oxygen involve in lithiation, but much of Li-N is irreversible. The excellent performances of CNFs film can be attributed to the N, O doped structure of graphite domain that has increased the conductivity and lithium storage ability. Further development of N, O doped CNFs may enable practical applications as flexible anode in high-performance lithium-ion batteries.

  16. Conceptual study on advanced PWR system

    Energy Technology Data Exchange (ETDEWEB)

    Bae, Yoon Young; Chang, M. H.; Yu, K. J.; Lee, D. J.; Cho, B. H.; Kim, H. Y.; Yoon, J. H.; Lee, Y. J.; Kim, J. P.; Park, C. T.; Seo, J. K.; Kang, H. S.; Kim, J. I.; Kim, Y. W.; Kim, Y. H.

    1997-07-01

    In this study, the adoptable essential technologies and reference design concept of the advanced reactor were developed and related basic experiments were performed. (1) Once-through Helical Steam Generator: a performance analysis computer code for heli-coiled steam generator was developed for thermal sizing of steam generator and determination of thermal-hydraulic parameters. (2) Self-pressurizing pressurizer : a performance analysis computer code for cold pressurizer was developed. (3) Control rod drive mechanism for fine control : type and function were surveyed. (4) CHF in passive PWR condition : development of the prediction model bundle CHF by introducing the correction factor from the data base. (5) Passive cooling concepts for concrete containment systems: development of the PCCS heat transfer coefficient. (6) Steam injector concepts: analysis and experiment were conducted. (7) Fluidic diode concepts : analysis and experiment were conducted. (8) Wet thermal insulator : tests for thin steel layers and assessment of materials. (9) Passive residual heat removal system : a performance analysis computer code for PRHRS was developed and the conformance to EPRI requirement was checked. (author). 18 refs., 55 tabs., 137 figs.

  17. High concentration nitrogen doped carbon nanotube anodes with superior Li+ storage performance for lithium rechargeable battery application

    Science.gov (United States)

    Li, Xifei; Liu, Jian; Zhang, Yong; Li, Yongliang; Liu, Hao; Meng, Xiangbo; Yang, Jinli; Geng, Dongsheng; Wang, Dongniu; Li, Ruying; Sun, Xueliang

    2012-01-01

    A floating catalyst chemical vapor deposition method has been developed to synthesize carbon nanotubes doped with a high concentration of nitrogen. Their electrochemical performance as anodes for lithium ion batteries (LIBs) in comparison to pristine carbon nanotubes (CNTs) has been investigated. X-ray photoelectron spectroscopy results indicated that the nitrogen content reaches as high as 16.4 at.%. Bamboo-like compartments were fabricated as shown by high resolution transmission electron microscopy. High concentration nitrogen doped carbon nanotubes (HN-CNTs) show approximately double reversible capacity of CNTs: 494 mAh g-1 vs. 260 mAh g-1, and present a much better rate capability than CNTs. The significantly superior electrochemical performance could be related to the high electrical conductivity and the larger number of defect sites in HN-CNTs for anodes of LIBs.

  18. Seismic qualification of PWR plant auxiliary feedwater systems

    Energy Technology Data Exchange (ETDEWEB)

    Lu, S.C.; Tsai, N.C.

    1983-08-01

    The NRC Standard Review Plan specifies that the auxiliary feedwater (AFW) system of a pressurized water reactor (PWR) is a safeguard system that functions in the event of a Safe Shutdown Earthquake (SSE) to remove the decay heat via the steam generator. Only recently licensed PWR plants have an AFW system designed to the current Standard Review Plan specifications. The NRC devised the Multiplant Action Plan C-14 in order to make a survey of the seismic capability of the AFW systems of operating PWR plants. The purpose of this survey is to enable the NRC to make decisions regarding the need of requiring the licensees to upgrade the AFW systems to an SSE level of seismic capability. To implement the first phase of the C-14 plan, the NRC issued a Generic Letter (GL) 81-14 to all operating PWR licensees requesting information on the seismic capability of their AFW systems. This report summarizes Lawrence Livermore National Laboratory's efforts to assist the NRC in evaluating the status of seismic qualification of the AFW systems in 40 PWR plants, by reviewing the licensees' responses to GL 81-14.

  19. Lithium nephrotoxicity.

    Science.gov (United States)

    Oliveira, Jobson Lopes de; Silva Júnior, Geraldo Bezerra da; Abreu, Krasnalhia Lívia Soares de; Rocha, Natália de Albuquerque; Franco, Luiz Fernando Leonavicius G; Araújo, Sônia Maria Holanda Almeida; Daher, Elizabeth de Francesco

    2010-01-01

    Lithium has been widely used in the treatment of bipolar disorder. Its renal toxicity includes impaired urinary concentrating ability and natriuresis, renal tubular acidosis, tubulointerstitial nephritis progressing to chronic kidney disease and hypercalcemia. The most common adverse effect is nephrogenic diabetes insipidus, which affects 20-40% of patients within weeks of lithium initiation. Chronic nephropathy correlates with duration of lithium therapy. Early detection of renal dysfunction should be achieved by rigorous monitoring of patients and close collaboration between psychiatrists and nephrologists. Recent experimental and clinical studies begin to clarify the mechanisms by which lithium induces changes in renal function. The aim of this study was to review the pathogenesis, clinical presentation, histopathological aspects and treatment of lithium-induced nephrotoxicity.

  20. Facile synthesis of uniform MWCNT@Si nanocomposites as high-performance anode materials for lithium-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Yifan; Du, Ning, E-mail: dna1122@zju.edu.cn; Zhang, Hui; Yang, Deren

    2015-02-15

    Highlights: • A uniform SiO{sub 2} layer was deposited on multi-walled carbon nanotube. • Synthesis of uniform (MWCNT)@Si nanocomposites via the magnesiothermic reduction. • The MWCNT@Si nanocomposites show high reversible capacity and good cyclability. • Enhanced performance is attributed to porous nanostructure, introduction of MWCNTs. - Abstract: We demonstrate the synthesis of uniform multi-walled carbon nanotube (MWCNT)@Si nanocomposites via the magnesiothermic reduction of pre-synthesized MWCNT@SiO{sub 2} nanocables. At first, the acid vapor steaming is used to treat the surface, which can facilitate the uniform deposition of SiO{sub 2} layer via the TEOS hydrolysis. Then, the uniform MWCNT@Si nanocomposites are obtained on the basis of MWCNT@SiO{sub 2} nanocables via a simple magnesiothermic reduction. When used as an anode material for lithium-ion batteries, the as-synthesized MWCNT@Si nanocomposites show high reversible capacity and good cycling performance, which is better than bulk Si and bare MWCNTs. It is believed that the good electrochemical performance can be attributed to the novel porous nanostructure and the introduction of MWCNTs that can buffer the volume change, maintain the electrical conductive network, and enhance the electronic conductivity and lithium-ion transport.

  1. Porous cellulose diacetate-SiO2 composite coating on polyethylene separator for high-performance lithium-ion battery.

    Science.gov (United States)

    Chen, Wenju; Shi, Liyi; Wang, Zhuyi; Zhu, Jiefang; Yang, Haijun; Mao, Xufeng; Chi, Mingming; Sun, Lining; Yuan, Shuai

    2016-08-20

    The developments of high-performance lithium ion battery are eager to the separators with high ionic conductivity and thermal stability. In this work, a new way to adjust the comprehensive properties of inorganic-organic composite separator was investigated. The cellulose diacetate (CDA)-SiO2 composite coating is beneficial for improving the electrolyte wettability and the thermal stability of separators. Interestingly, the pore structure of composite coating can be regulated by the weight ratio of SiO2 precursor tetraethoxysilane (TEOS) in the coating solution. The electronic performance of lithium ion batteries assembled with modified separators are improved compared with the pristine PE separator. When weight ratio of TEOS in the coating solution was 9.4%, the composite separator shows the best comprehensive performance. Compared with the pristine PE separator, its meltdown temperature and the break-elongation at elevated temperature increased. More importantly, the discharge capacity and the capacity retention improved significantly. Copyright © 2016 Elsevier Ltd. All rights reserved.

  2. Attainable high capacity in Li-excess Li-Ni-Ru-O rock-salt cathode for lithium ion battery

    Science.gov (United States)

    Wang, Xingbo; Huang, Weifeng; Tao, Shi; Xie, Hui; Wu, Chuanqiang; Yu, Zhen; Su, Xiaozhi; Qi, Jiaxin; Rehman, Zia ur; Song, Li; Zhang, Guobin; Chu, Wangsheng; Wei, Shiqiang

    2017-08-01

    Peroxide structure O2n- has proven to appear after electrochemical process in many lithium-excess precious metal oxides, representing extra reversible capacity. We hereby report construction of a Li-excess rock-salt oxide Li1+xNi1/2-3x/2Ru1/2+x/2O2 electrode, with cost effective and eco-friendly 3d transition metal Ni partially substituting precious 4d transition metal Ru. It can be seen that O2n- is formed in pristine Li1.23Ni0.155Ru0.615O2, and stably exists in subsequent cycles, enabling discharge capacities to 295.3 and 198 mAh g-1 at the 1st/50th cycle, respectively. Combing ex-situ X-ray absorption near edge spectroscopy, X-ray photoelectron spectroscopy, X-ray diffraction, high resolution transmission electron microscopy and electrochemical characterization, we demonstrate that the excellent electrochemical performance comes from both percolation network with disordered structure and cation/anion redox couples occurring in charge-discharge process. Li-excess and substitution of common element have been demonstrated to be a breakthrough for designing novel high performance commercial cathodes in rechargeable lithium ion battery field.

  3. A silicon nanowire-reduced graphene oxide composite as a high-performance lithium ion battery anode material.

    Science.gov (United States)

    Ren, Jian-Guo; Wang, Chundong; Wu, Qi-Hui; Liu, Xiang; Yang, Yang; He, Lifang; Zhang, Wenjun

    2014-03-21

    Toward the increasing demands of portable energy storage and electric vehicle applications, silicon has been emerging as a promising anode material for lithium-ion batteries (LIBs) owing to its high specific capacity. However, serious pulverization of bulk silicon during cycling limits its cycle life. Herein, we report a novel hierarchical Si nanowire (Si NW)-reduced graphene oxide (rGO) composite fabricated using a solvothermal method followed by a chemical vapor deposition process. In the composite, the uniform-sized [111]-oriented Si NWs are well dispersed on the rGO surface and in between rGO sheets. The flexible rGO enables us to maintain the structural integrity and to provide a continuous conductive network of the electrode, which results in over 100 cycles serving as an anode in half cells at a high lithium storage capacity of 2300 mA h g(-1). Due to its [111] growth direction and the large contact area with rGO, the Si NWs in the composite show substantially enhanced reaction kinetics compared with other Si NWs or Si particles.

  4. Optimization of Acetylene Black Conductive Additive andPolyvinylidene Difluoride Composition for High Power RechargeableLithium-Ion Cells

    Energy Technology Data Exchange (ETDEWEB)

    Liu, G.; Zheng, H.; Battaglia, V.S.; Simens, A.S.; Minor, A.M.; Song, X.

    2007-07-01

    Fundamental electrochemical methods were applied to study the effect of the acetylene black (AB) and the polyvinylidene difluoride (PVDF) polymer binder on the performance of high-power designed rechargeable lithium ion cells. A systematic study of the AB/PVDF long-range electronic conductivity at different weight ratios is performed using four-probe direct current tests and the results reported. There is a wide range of AB/PVDF ratios that satisfy the long-range electronic conductivity requirement of the lithium-ion cathode electrode; however, a significant cell power performance improvement is observed at small AB/PVDF composition ratios that are far from the long-range conductivity optimum of 1 to 1.25. Electrochemical impedance spectroscopy (EIS) tests indicate that the interfacial impedance decreases significantly with increase in binder content. The hybrid power pulse characterization results agree with the EIS tests and also show improvement for cells with a high PVDF content. The AB to PVDF composition plays a significant role in the interfacial resistance. We believe the higher binder contents lead to a more cohesive conductive carbon particle network that results in better overall all local electronic conductivity on the active material surface and hence reduced charge transfer impedance.

  5. Three-dimensional high resolution X-ray imaging and quantification of lithium ion battery mesocarbon microbead anodes

    Science.gov (United States)

    Tariq, F.; Yufit, V.; Kishimoto, M.; Shearing, P. R.; Menkin, S.; Golodnitsky, D.; Gelb, J.; Peled, E.; Brandon, N. P.

    2014-02-01

    In order to improve lithium ion batteries it is important to characterise real electrode geometries and understand how their 3D structure may affect performance. In this study, high resolution synchrotron nano-CT was used to acquire 3D tomography datasets of mesocarbon microbead (MCMB) based anodes down to a 16 nm voxel size. A specimen labelling methodology was used to produce anodes that enhance the achievable image contrast, and image processing routines were utilised to successfully segment features of interest from a challenging dataset. The 3D MCMB based anode structure was analysed revealing a heterogeneous and bi-modally distributed microstructure. The microstructure was quantified through calculations of surface area, volume, connectivity and tortuosity factors. In doing so, two different methods, random walk and diffusion based, were used to determine tortuosity factors of both MCMB and pore/electrolyte microstructures. The tortuosity factors (2-7) confirmed the heterogeneity of the anode microstructure for this field of view and demonstrated small MCMB particles interspersed between large MCMB particles cause an increase in tortuosity factors. The anode microstructure was highly connected, which was also caused by the presence of small MCMB particles. The complexity in microstructure suggests inhomogeneous local lithium ion distribution would occur within the anode during operation.

  6. Electrospun CuFe2O4 nanotubes as anodes for high-performance lithium-ion batteries

    Institute of Scientific and Technical Information of China (English)

    Shengjie Peng; Linlin Li; Madhavi Srinivasan

    2014-01-01

    Herein, we report on the synthesis and lithium storage properties of electrospun one-dimensional (1D) CuFe2O4 nanomaterials. 1D CuFe2O4 nanotubes and nanorods were fabricated by a single spinneret electrospinning method followed by thermal decomposition for removal of polymers from the precursor fibers. The as-prepared CuFe2O4 nanotubes with wall thickness of∼50 nm presented diameters of∼150 nm and lengths up to several millimeters. It was found that phase separation between the electrospun composite materials occured during the electrospinning process, while the as-spun precursor nanofibers composed of polyacrylonitrile (PAN), polyvinylpyrrolidone (PVP) and metal salts might possess a core-shell structure (PAN as the core and PVP/metal salts composite as the shell) and then transformed to a hollow structure after calcination. Moreover, as a demonstration of the functional properties of the 1D nanostructure, CuFe2 O4 nanotubes and nanorods were investigated as anodes for lithium ion batteries (LIBs). It was demonstrated that CuFe2O4 nanotubes not only delivered a high reversible capacity of ∼816 mAh·g-1 at a current density of 200 mA·g-1 over 50 cycles, but also showed superior rate capability with respect to counterpart nanorods. Probably, the enhanced electrochemical performance can be attributed to its high specific surface areas as well as the unique hollow structure.

  7. High-power durability of LiCoO2 thin film electrode modified with amorphous lithium tungsten oxide

    Science.gov (United States)

    Hayashi, Tetsutaro; Matsuda, Yasutaka; Kuwata, Naoaki; Kawamura, Junichi

    2017-06-01

    To investigate electrochemical performances of an amorphous lithium tungsten oxide (LWO) layer, an amorphous LWO-modified LiCoO2 (LCO) thin film electrode is fabricated by pulsed laser deposition and is exposed under a humid environment. The amorphous LWO-modified LCO exhibits high capacity retention of 80% at a rapid charge-discharge rate of 20 C. Conversely, the bare LCO exhibits capacity retention of 0% at the rates of 20 C. Electrochemical impedance spectroscopy demonstrates that the LWO-modified LCO maintains a low interfacial resistance after the cycling test compared with the bare LCO. X-ray photoemission spectroscopy (XPS), scanning transmission microscopy (STEM), and electron energy loss spectroscopy (EELS) indicate the presence of Li2CO3 on the surface of the bare LCO electrode and a thick degraded surface layer of CoO structure on the surface of LCO primary particle after electrochemical tests. XPS, STEM, and EELS indicate the presence of low amounts of Li2CO3 on the surface of the LWO-modified LCO, the LCO layer remains in a normal state, and LWO layer maintains the amorphous LWO state after the tests. Thus, the amorphous LWO protective layer contributes to suppressing the degradation of LCO and maintaining an amorphous LWO state with a lithium ion conductor, resulting in high-power durability.

  8. MOF-derived ultrafine MnO nanocrystals embedded in a porous carbon matrix as high-performance anodes for lithium-ion batteries

    Science.gov (United States)

    Zheng, Fangcai; Xia, Guoliang; Yang, Yang; Chen, Qianwang

    2015-05-01

    Although MnO has been demonstrated to be a promising anode material for lithium-ion batteries (LIBs) in terms of its high theoretical capacity (755 mA h g-1), comparatively low voltage hysteresis (storage applications.Although MnO has been demonstrated to be a promising anode material for lithium-ion batteries (LIBs) in terms of its high theoretical capacity (755 mA h g-1), comparatively low voltage hysteresis (storage applications. Electronic supplementary information (ESI) available. See DOI: 10.1039/c5nr00528k

  9. Sealed Primary Lithium-Inorganic Electrolyte Cell

    Science.gov (United States)

    1977-02-01

    Battery , Thionyl Chloride , Lithium , Lithium Aluminum Chloride , Hermetic Lithium Battery , D Cell, Voltage-Delay, Shelf Life, High Energy Density Battery ... lithium - thionyl chloride , inorganic electrclyte system is one of the highest energy density systems known to date (1-4). The cells contain an Li anoae, a...However, this is not tne case with te thionyl chloride system. A completely discharged battery , while sitting on

  10. Aqueous Nanofluid as a Two-Phase Coolant for PWR

    Directory of Open Access Journals (Sweden)

    Pavel N. Alekseev

    2012-01-01

    Full Text Available Density fluctuations in liquid water consist of two topological kinds of instant molecular clusters. The dense ones have helical hydrogen bonds and the nondense ones are tetrahedral clusters with ice-like hydrogen bonds of water molecules. Helical ordering of protons in the dense water clusters can participate in coherent vibrations. The ramified interface of such incompatible structural elements induces clustering impurities in any aqueous solution. These additives can enhance a heat transfer of water as a two-phase coolant for PWR due to natural forming of nanoparticles with a thermal conductivity higher than water. The aqueous nanofluid as a new condensed matter has a great potential for cooling applications. It is a mixture of liquid water and dispersed phase of extremely fine quasi-solid particles usually less than 50 nm in size with the high thermal conductivity. An alternative approach is the formation of gaseous (oxygen or hydrogen nanoparticles in density fluctuations of water. It is possible to obtain stable nanobubbles that can considerably exceed the molecular solubility of oxygen (hydrogen in water. Such a nanofluid can convert the liquid water in the nonstoichiometric state and change its reduction-oxidation (RedOx potential similarly to adding oxidants (or antioxidants for applying 2D water chemistry to aqueous coolant.

  11. PWR safety/relief valve blowdown analysis experience

    Energy Technology Data Exchange (ETDEWEB)

    Lee, M.Z.; Chou, L.Y.; Yang, S.H. (Gilbert/Commonwealth Engineers and Consultants, Reading, PA (USA). Speciality Engineering Dept.)

    1982-10-01

    The paper describes the difficulties encountered in analyzing a PWR primary loop pressurizer safety relief valve and power operated relief valve discharge system, as well as their resolution. The experience is based on the use of RELAP5/MOD1 and TPIPE computer programs as the tools for fluid transient analysis and piping dynamic analysis, respectively. General approaches for generating forcing functions from thermal fluid analysis solution to be used in the dynamic analysis of piping are reviewed. The paper demonstrates that the 'acceleration or wave force' method may have numerical difficulties leading to unrealistic, large amplitude, highly oscillatory forcing functions in the vicinity of severe flow area discontinuities or choking junctions when low temperature loop seal water is discharged. To avoid this problem, an alternate computational method based on the direct force method may be used. The simplicity and superiority in numerical stability of the forcing function computation method as well as its drawbacks are discussed. Additionally, RELAP modeling for piping, valve, reducer, and sparger is discussed. The effects of loop seal temperature on SRV and PORV discharge line blowdown forces, pressure and temperature distributions are examined. Finally, the effects of including support stiffness and support eccentricity in piping analysis models, method and modeling relief tank connections, minimization of tank nozzle loads, use of damping factors, and selection of solution time steps are discussed.

  12. The advanced main control console for next japanese PWR plants

    Energy Technology Data Exchange (ETDEWEB)

    Tsuchiya, A. [Hokkaido Electric Power Co., Inc., Sapporo (Japan); Ito, K. [Mitsubishi Heavy Industries, Ltd., Nuclear Energy Systems Engineering Center, Yokohama (Japan); Yokoyama, M. [Mitsubishi Electric Corporation, Energy and Industrial Systems Center, Kobe (Japan)

    2001-07-01

    The purpose of the improvement of main control room designing in a nuclear power plant is to reduce operators' workload and potential human errors by offering a better working environment where operators can maximize their abilities. In order to satisfy such requirements, the design of main control board applied to Japanese Pressurized Water Reactor (PWR) type nuclear power plant has been continuously modified and improved. the Japanese Pressurized Water Reactor (PWR) Utilities (Electric Power Companies) and Mitsubishi Group have developed an advanced main control board (console) reflecting on the study of human factors, as well as using a state of the art electronics technology. In this report, we would like to introduce the configuration and features of the Advanced Main Control Console for the practical application to the next generation PWR type nuclear power plants including TOMARI No.3 Unit of Hokkaido Electric Power Co., Inc. (author)

  13. Structural optimization of 3D porous electrodes for high-rate performance lithium ion batteries.

    Science.gov (United States)

    Ye, Jianchao; Baumgaertel, Andreas C; Wang, Y Morris; Biener, Juergen; Biener, Monika M

    2015-02-24

    Much progress has recently been made in the development of active materials, electrode morphologies and electrolytes for lithium ion batteries. Well-defined studies on size effects of the three-dimensional (3D) electrode architecture, however, remain to be rare due to the lack of suitable material platforms where the critical length scales (such as pore size and thickness of the active material) can be freely and deterministically adjusted over a wide range without affecting the overall 3D morphology of the electrode. Here, we report on a systematic study on length scale effects on the electrochemical performance of model 3D np-Au/TiO2 core/shell electrodes. Bulk nanoporous gold provides deterministic control over the pore size and is used as a monolithic metallic scaffold and current collector. Extremely uniform and conformal TiO2 films of controlled thickness were deposited on the current collector by employing atomic layer deposition (ALD). Our experiments demonstrate profound performance improvements by matching the Li(+) diffusivity in the electrolyte and the solid state through adjusting pore size and thickness of the active coating which, for 200 μm thick porous electrodes, requires the presence of 100 nm pores. Decreasing the thickness of the TiO2 coating generally improves the power performance of the electrode by reducing the Li(+) diffusion pathway, enhancing the Li(+) solid solubility, and minimizing the voltage drop across the electrode/electrolyte interface. With the use of the optimized electrode morphology, supercapacitor-like power performance with lithium-ion-battery energy densities was realized. Our results provide the much-needed fundamental insight for the rational design of the 3D architecture of lithium ion battery electrodes with improved power performance.

  14. ESTABLISHING SUSTAINABLE US HEV/PHEV MANUFACTURING BASE: STABILIZED LITHIUM METAL POWDER, ENABLING MATERIAL AND REVOLUTIONARY TECHNOLOGY FOR HIGH ENERGY LI-ION BATTERIES

    Energy Technology Data Exchange (ETDEWEB)

    Yakovleva, Marina

    2012-12-31

    FMC Lithium Division has successfully completed the project “Establishing Sustainable US PHEV/EV Manufacturing Base: Stabilized Lithium Metal Powder, Enabling Material and Revolutionary Technology for High Energy Li-ion Batteries”. The project included design, acquisition and process development for the production scale units to 1) produce stabilized lithium dispersions in oil medium, 2) to produce dry stabilized lithium metal powders, 3) to evaluate, design and acquire pilot-scale unit for alternative production technology to further decrease the cost, and 4) to demonstrate concepts for integrating SLMP technology into the Li- ion batteries to increase energy density. It is very difficult to satisfy safety, cost and performance requirements for the PHEV and EV applications. As the initial step in SLMP Technology introduction, industry can use commercially available LiMn2O4 or LiFePO4, for example, that are the only proven safer and cheaper lithium providing cathodes available on the market. Unfortunately, these cathodes alone are inferior to the energy density of the conventional LiCoO2 cathode and, even when paired with the advanced anode materials, such as silicon composite material, the resulting cell will still not meet the energy density requirements. We have demonstrated, however, if SLMP Technology is used to compensate for the irreversible capacity in the anode, the efficiency of the cathode utilization will be improved and the cost of the cell, based on the materials, will decrease.

  15. Reserve lithium-thionyl chloride battery for high rate extended mission applications

    Science.gov (United States)

    Peabody, Mark; Brown, Robert A.

    An effort has been made to develop technology for lithium-thionyl chloride batteries whose emission times will extend beyond 20 min and whose power levels will be in excess of 1800 W, using the requirements for an existing silver-zinc battery's electrical requirements as a baseline. The target design encompasses separate 31- and 76-V sections; the design goal was the reduction of battery weight to 50 percent that of the present silver/zinc cell. A cell has been achieved whose mission can be conducted without container heat losses.

  16. High Temperature Stable Separator for Lithium Batteries Based on SiO2 and Hydroxypropyl Guar Gum

    Science.gov (United States)

    Carvalho, Diogo Vieira; Loeffler, Nicholas; Kim, Guk-Tae; Passerini, Stefano

    2015-01-01

    A novel membrane based on silicon dioxide (SiO2) and hydroxypropyl guar gum (HPG) as binder is presented and tested as a separator for lithium-ion batteries. The separator is made with renewable and low cost materials and an environmentally friendly manufacturing processing using only water as solvent. The separator offers superior wettability and high electrolyte uptake due to the optimized porosity and the good affinity of SiO2 and guar gum microstructure towards organic liquid electrolytes. Additionally, the separator shows high thermal stability and no dimensional-shrinkage at high temperatures due to the use of the ceramic filler and the thermally stable natural polymer. The electrochemical tests show the good electrochemical stability of the separator in a wide range of potential, as well as its outstanding cycle performance. PMID:26512701

  17. High Temperature Stable Separator for Lithium Batteries Based on SiO2 and Hydroxypropyl Guar Gum

    Directory of Open Access Journals (Sweden)

    Diogo Vieira Carvalho

    2015-10-01

    Full Text Available A novel membrane based on silicon dioxide (SiO2 and hydroxypropyl guar gum (HPG as binder is presented and tested as a separator for lithium-ion batteries. The separator is made with renewable and low cost materials and an environmentally friendly manufacturing processing using only water as solvent. The separator offers superior wettability and high electrolyte uptake due to the optimized porosity and the good affinity of SiO2 and guar gum microstructure towards organic liquid electrolytes. Additionally, the separator shows high thermal stability and no dimensional-shrinkage at high temperatures due to the use of the ceramic filler and the thermally stable natural polymer. The electrochemical tests show the good electrochemical stability of the separator in a wide range of potential, as well as its outstanding cycle performance.

  18. A novel high-performance gel polymer electrolyte membrane basing on electrospinning technique for lithium rechargeable batteries

    Science.gov (United States)

    Wu, Na; Cao, Qi; Wang, Xianyou; Li, Xiaoyun; Deng, Huayang

    2011-10-01

    Nonwoven films of composites of thermoplastic polyurethane (TPU) with different proportion of poly(vinylidene fluoride) (PVdF) (80, 50 and 20%, w/w) are prepared by electrospinning 9 wt% polymer solution at room temperature. Then the gel polymer electrolytes (GPEs) are prepared by soaking the electrospun TPU-PVdF blending membranes in 1 M LiClO4/ethylene carbonate (EC)/propylene carbonate (PC) for 1 h. The gel polymer electrolyte (GPE) shows a maximum ionic conductivity of 3.2 × 10-3 S cm-1 at room temperature and electrochemical stability up to 5.0 V versus Li+/Li for the 50:50 blend ratio of TPU:PVdF system. At the first cycle, it shows a first charge-discharge capacity of 168.9 mAh g-1 when the gel polymer electrolyte (GPE) is evaluated in a Li/PE/lithium iron phosphate (LiFePO4) cell at 0.1 C-rate at 25 °C. TPU-PVdF (50:50, w/w) based gel polymer electrolyte is observed much more suitable than the composite films with other ratios for high-performance lithium rechargeable batteries.

  19. Density functional theory screening of gas-treatment strategies for stabilization of high energy-density lithium metal anodes

    Science.gov (United States)

    Koch, Stephan L.; Morgan, Benjamin J.; Passerini, Stefano; Teobaldi, Gilberto

    2015-11-01

    To explore the potential of molecular gas treatment of freshly cut lithium foils in non-electrolyte-based passivation of high-energy-density Li anodes, density functional theory (DFT) has been used to study the decomposition of molecular gases on metallic lithium surfaces. By combining DFT geometry optimization and Molecular Dynamics, the effects of atmospheric (N2, O2, CO2) and hazardous (F2, SO2) gas decomposition on Li(bcc) (100), (110), and (111) surfaces on relative surface energies, work functions, and emerging electronic and elastic properties are investigated. The simulations suggest that exposure to different molecular gases can be used to induce and control reconstructions of the metal Li surface and substantial changes (up to over 1 eV) in the work function of the passivated system. Contrary to the other considered gases, which form metallic adlayers, SO2 treatment emerges as the most effective in creating an insulating passivation layer for dosages ≤1 mono-layer. The substantial Li → adsorbate charge transfer and adlayer relaxation produce marked elastic stiffening of the interface, with the smallest change shown by nitrogen-treated adlayers.

  20. Three dimensional Graphene aerogels as binder-less, freestanding, elastic and high-performance electrodes for lithium-ion batteries

    Science.gov (United States)

    Chen, Zhihang; Li, Hua; Tian, Ran; Duan, Huanan; Guo, Yiping; Chen, Yujie; Zhou, Jie; Zhang, Chunmei; Dugnani, Roberto; Liu, Hezhou

    2016-06-01

    In this work it is shown how porous graphene aerogels fabricated by an eco-friendly and simple technological process, could be used as electrodes in lithium- ion batteries. The proposed graphene framework exhibited excellent performance including high reversible capacities, superior cycling stability and rate capability. A significantly lower temperature (75 °C) than the one currently utilized in battery manufacturing was utilized for self-assembly hence providing potential significant savings to the industrial production. After annealing at 600 °C, the formation of Sn-C-O bonds between the SnO2 nanoparticles and the reduced graphene sheets will initiate synergistic effect and improve the electrochemical performance. The XPS patterns revealed the formation of Sn-C-O bonds. Both SEM and TEM imaging of the electrode material showed that the three dimensional network of graphene aerogels and the SnO2 particles were distributed homogeneously on graphene sheets. Finally, the electrochemical properties of the samples as active anode materials for lithium-ion batteries were tested and examined by constant current charge-discharge cycling and the finding fully described in this manuscript.

  1. Novel choline-based ionic liquids as safe electrolytes for high-voltage lithium-ion batteries

    Science.gov (United States)

    Yong, Tianqiao; Zhang, Lingzhi; Wang, Jinglun; Mai, Yongjin; Yan, Xiaodan; Zhao, Xinyue

    2016-10-01

    Three choline-based ionic liquids functionalized with trimethylsilyl, allyl, and cynoethyl groups are synthesized in an inexpensive route as safe electrolytes for high-voltage lithium-ion batteries. The thermal stabilities, viscosities, conductivities, and electrochemical windows of these ILs are reported. Hybrid electrolytes were formulated by doping with 0.6 M LiPF6/0.4 M lithium oxalydifluoroborate (LiODFB) as salts and dimethyl carbonate (DMC) as co-solvent. By using 0.6 M LiPF6/0.4 M LiODFB trimethylsilylated choline-based IL (SN1IL-TFSI)/DMC as electrolyte, LiCoO2/graphite full cell showed excellent cycling performance with a capacity of 152 mAh g-1 and 99% capacity retention over 90 cycles at a cut-off voltage of 4.4 V. The propagation rate of SN1IL-TFSI)/DMC electrolyte is only one quarter of the commercial electrolyte (1 M LiPF6 EC/DEC/DMC, v/v/v = 1/1/1), suggesting a better safety feature.

  2. Onion-like carbon coated CuO nanocapsules: A highly reversible anode material for lithium ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Xianguo, E-mail: liuxianguohugh@gmail.com [Anhui Key Laboratory of Metal Materials and Processing, School of Materials Science and Engineering, Anhui University of Technology, Maanshan 243002 (China); Bi, Nannan; Feng, Chao [Anhui Key Laboratory of Metal Materials and Processing, School of Materials Science and Engineering, Anhui University of Technology, Maanshan 243002 (China); Or, Siu Wing [Department of Electrical Engineering, The Hong Kong Polytechnic University, Hung Hom, Kowloon (Hong Kong); Sun, Yuping [Center for Engineering practice and Innovation Education, Anhui University of Technology, Maanshan 243002 (China); Jin, Chuangui; Li, Weihuo; Xiao, Feng [Anhui Key Laboratory of Metal Materials and Processing, School of Materials Science and Engineering, Anhui University of Technology, Maanshan 243002 (China)

    2014-02-25

    Highlights: • Onion-like carbon–coated CuO nanocapsules have been synthesized. • Onion-like carbon leads to the improved stability and electric conductivity. • CuO/C nanocapsules maintain a reversible capacity of 628.7 mA h g{sup −1} after 50 cycles. -- Abstract: The synthesis and characterization of CuO/C nanocapsules for application as anode material in lithium ion batteries are reported. Introduction of onion-like carbon shell on the CuO nanoparticles leads to the improved stability, electric conductivity and electrochemical performance. When evaluated as potential anode materials for lithium-ion batteries, the novel CuO/C nanocapsules deliver an initial discharge capacity of 1043.9 mA h g{sup −1} at 100 mA g{sup −1} and maintain a high reversible capacity of 628.7 mA h g{sup −1} after 50 charge–discharge cycles, much higher than those of the CuO nanoparticles. A postmortem analysis of the CuO and CuO/C anodes subjected to prolonged cycling reveals the existence of a lower degree of surface cracking and particle breakage in the CuO/C anode than the CuO anode.

  3. Three dimensional Graphene aerogels as binder-less, freestanding, elastic and high-performance electrodes for lithium-ion batteries

    Science.gov (United States)

    Chen, Zhihang; Li, Hua; Tian, Ran; Duan, Huanan; Guo, Yiping; Chen, Yujie; Zhou, Jie; Zhang, Chunmei; DUGNANI, Roberto; Liu, Hezhou

    2016-01-01

    In this work it is shown how porous graphene aerogels fabricated by an eco-friendly and simple technological process, could be used as electrodes in lithium- ion batteries. The proposed graphene framework exhibited excellent performance including high reversible capacities, superior cycling stability and rate capability. A significantly lower temperature (75 °C) than the one currently utilized in battery manufacturing was utilized for self-assembly hence providing potential significant savings to the industrial production. After annealing at 600 °C, the formation of Sn-C-O bonds between the SnO2 nanoparticles and the reduced graphene sheets will initiate synergistic effect and improve the electrochemical performance. The XPS patterns revealed the formation of Sn-C-O bonds. Both SEM and TEM imaging of the electrode material showed that the three dimensional network of graphene aerogels and the SnO2 particles were distributed homogeneously on graphene sheets. Finally, the electrochemical properties of the samples as active anode materials for lithium-ion batteries were tested and examined by constant current charge–discharge cycling and the finding fully described in this manuscript. PMID:27265146

  4. Three dimensional Graphene aerogels as binder-less, freestanding, elastic and high-performance electrodes for lithium-ion batteries.

    Science.gov (United States)

    Chen, Zhihang; Li, Hua; Tian, Ran; Duan, Huanan; Guo, Yiping; Chen, Yujie; Zhou, Jie; Zhang, Chunmei; Dugnani, Roberto; Liu, Hezhou

    2016-06-06

    In this work it is shown how porous graphene aerogels fabricated by an eco-friendly and simple technological process, could be used as electrodes in lithium- ion batteries. The proposed graphene framework exhibited excellent performance including high reversible capacities, superior cycling stability and rate capability. A significantly lower temperature (75 °C) than the one currently utilized in battery manufacturing was utilized for self-assembly hence providing potential significant savings to the industrial production. After annealing at 600 °C, the formation of Sn-C-O bonds between the SnO2 nanoparticles and the reduced graphene sheets will initiate synergistic effect and improve the electrochemical performance. The XPS patterns revealed the formation of Sn-C-O bonds. Both SEM and TEM imaging of the electrode material showed that the three dimensional network of graphene aerogels and the SnO2 particles were distributed homogeneously on graphene sheets. Finally, the electrochemical properties of the samples as active anode materials for lithium-ion batteries were tested and examined by constant current charge-discharge cycling and the finding fully described in this manuscript.

  5. Control of Internal and External Short Circuits in Lithium Ion and Lithium Batteries Project

    Data.gov (United States)

    National Aeronautics and Space Administration — NASA has identified needs for compact high-energy-density primary and secondary batteries. Lithium and Lithium Ion cells, respectively, are meeting these needs for...

  6. Evaluation of PWR and BWR pin cell benchmark results

    Energy Technology Data Exchange (ETDEWEB)

    Pijlgroms, B.J.; Gruppelaar, H.; Janssen, A.J. (Unit Nuclear Energy, Netherlands Energy Research Foundation ECN, Petten (Netherlands)); Hoogenboorm, J.E.; De Leege, P.F.A. (International Reactor Institute IRI, University of Leiden, Leiden (Netherlands)); Van de Voet, J.; Verhagen, F.C.M. (KEMA NV, Arnhem (Netherlands))

    1992-01-01

    In order to carry out reliable reactor core calculations for a boiled water reactor (BWR) or a pressurized water reactor (PWR) first reactivity calculations have to be carried out for which several calculation programs are available. The purpose of the title project is to exchange experiences to improve the knowledge of this reactivity calculations. In a large number of institutes reactivity calculations of PWR and BWR pin cells were executed by means of available computer codes. Results are compared. It is concluded that the variations in the calculated results are problem dependent. Part of the results is satisfactory. However, further research is necessary.

  7. Monte Carlo based radial shield design of typical PWR reactor

    Energy Technology Data Exchange (ETDEWEB)

    Gul, Anas; Khan, Rustam; Qureshi, M. Ayub; Azeem, Muhammad Waqar; Raza, S.A. [Pakistan Institute of Engineering and Applied Sciences, Islamabad (Pakistan). Dept. of Nuclear Engineering; Stummer, Thomas [Technische Univ. Wien (Austria). Atominst.

    2016-11-15

    Neutron and gamma flux and dose equivalent rate distribution are analysed in radial and shields of a typical PWR type reactor based on the Monte Carlo radiation transport computer code MCNP5. The ENDF/B-VI continuous energy cross-section library has been employed for the criticality and shielding analysis. The computed results are in good agreement with the reference results (maximum difference is less than 56 %). It implies that MCNP5 a good tool for accurate prediction of neutron and gamma flux and dose rates in radial shield around the core of PWR type reactors.

  8. Leak before break application in French PWR plants under operation

    Energy Technology Data Exchange (ETDEWEB)

    Faidy, C. [EDF SEPTEN, Villeurbanne (France)

    1997-04-01

    Practical applications of the leak-before break concept are presently limited in French Pressurized Water Reactors (PWR) compared to Fast Breeder Reactors. Neithertheless, different fracture mechanic demonstrations have been done on different primary, auxiliary and secondary PWR piping systems based on similar requirements that the American NUREG 1061 specifications. The consequences of the success in different demonstrations are still in discussion to be included in the global safety assessment of the plants, such as the consequences on in-service inspections, leak detection systems, support optimization,.... A large research and development program, realized in different co-operative agreements, completes the general approach.

  9. Advanced ion exchange resins for PWR condensate polishing

    Energy Technology Data Exchange (ETDEWEB)

    Hoffman, B. [Rohm and Haas Co. (United States); Tsuzuki, S. [Rohm and Haas Co. (Japan)

    2002-07-01

    The severe chemical and mechanical requirements of a pressurized water reactor (PWR) condensate polishing plant (CPP) present a major challenge to the design of ion exchange resins. This paper describes the development and initial operating experience of improved cation and anion exchange resins that were specifically designed to meet PWR CPP needs. Although this paper focuses specifically on the ion exchange resins and their role in plant performance, it is also recognized and acknowledged that excellent mechanical design and operation of the CPP system are equally essential to obtaining good results. (authors)

  10. A Mo2C/Carbon Nanotube Composite Cathode for Lithium-Oxygen Batteries with High Energy Efficiency and Long Cycle Life.

    Science.gov (United States)

    Kwak, Won-Jin; Lau, Kah Chun; Shin, Chang-Dae; Amine, Khalil; Curtiss, Larry A; Sun, Yang-Kook

    2015-04-28

    Although lithium-oxygen batteries are attracting considerable attention because of the potential for an extremely high energy density, their practical use has been restricted owing to a low energy efficiency and poor cycle life compared to lithium-ion batteries. Here we present a nanostructured cathode based on molybdenum carbide nanoparticles (Mo2C) dispersed on carbon nanotubes, which dramatically increase the electrical efficiency up to 88% with a cycle life of more than 100 cycles. We found that the Mo2C nanoparticle catalysts contribute to the formation of well-dispersed lithium peroxide nanolayers (Li2O2) on the Mo2C/carbon nanotubes with a large contact area during the oxygen reduction reaction (ORR). This Li2O2 structure can be decomposed at low potential upon the oxygen evolution reaction (OER) by avoiding the energy loss associated with the decomposition of the typical Li2O2 discharge products.

  11. Removing hydrochloric acid exhaust products from high performance solid rocket propellant using aluminum-lithium alloy.

    Science.gov (United States)

    Terry, Brandon C; Sippel, Travis R; Pfeil, Mark A; Gunduz, I Emre; Son, Steven F

    2016-11-05

    Hydrochloric acid (HCl) pollution from perchlorate based propellants is well known for both launch site contamination, as well as the possible ozone layer depletion effects. Past efforts in developing environmentally cleaner solid propellants by scavenging the chlorine ion have focused on replacing a portion of the chorine-containing oxidant (i.e., ammonium perchlorate) with an alkali metal nitrate. The alkali metal (e.g., Li or Na) in the nitrate reacts with the chlorine ion to form an alkali metal chloride (i.e., a salt instead of HCl). While this technique can potentially reduce HCl formation, it also results in reduced ideal specific impulse (ISP). Here, we show using thermochemical calculations that using aluminum-lithium (Al-Li) alloy can reduce HCl formation by more than 95% (with lithium contents ≥15 mass%) and increase the ideal ISP by ∼7s compared to neat aluminum (using 80/20 mass% Al-Li alloy). Two solid propellants were formulated using 80/20 Al-Li alloy or neat aluminum as fuel additives. The halide scavenging effect of Al-Li propellants was verified using wet bomb combustion experiments (75.5±4.8% reduction in pH, ∝ [HCl], when compared to neat aluminum). Additionally, no measurable HCl evolution was detected using differential scanning calorimetry coupled with thermogravimetric analysis, mass spectrometry, and Fourier transform infrared absorption. Copyright © 2016 Elsevier B.V. All rights reserved.

  12. A new oxyfluorinated titanium phosphate anode for a high-energy lithium-ion battery.

    Science.gov (United States)

    Ma, Zhaohui; Sun, Chunwen; Lyu, Yingchun; Wang, Yuesheng; Kim, Youngsik; Chen, Liquan

    2015-01-21

    Na3[Ti2P2O10F] was synthesized by a hydrothermal method. It has an open framework structure consisting of TiFO5 octahedra and PO4 tetrahedra. The feasibility of Na3[Ti2P2O10F] as an anode material for lithium-ion batteries was first studied. Na3[Ti2P2O10F] exhibits a reversible capacity of more than 200 mAh g(-1) at a discharge/charge current rate of 20 mA g(-1) (∼0.1 C) and 105 mA g(-1) at a discharge/charge current rate of 400 mA g(-1) (∼2 C) with a lower intercalation voltage. The result of in situ X-ray diffraction test shows the structural evolution during the first discharge/charge cycle. The structure of Na3[Ti2P2O10F] was kept during discharge/charge with a slight change of the lattice parameters, which indicates a lithium solid solution behavior.

  13. Development of a high energy pulsed plasma simulator for the study of liquid lithium trenches

    Energy Technology Data Exchange (ETDEWEB)

    Jung, S., E-mail: jung73@illinois.edu [Department of Nuclear, Plasma, and Radiological Engineering, University of Illinois at Urbana-Champaign, Urbana 61801 (United States); Christenson, M.; Curreli, D. [Department of Nuclear, Plasma, and Radiological Engineering, University of Illinois at Urbana-Champaign, Urbana 61801 (United States); Bryniarski, C. [Department of Electrical and Computer Engineering, University of Illinois at Urbana-Champaign, Urbana 61801 (United States); Andruczyk, D.; Ruzic, D.N. [Department of Nuclear, Plasma, and Radiological Engineering, University of Illinois at Urbana-Champaign, Urbana 61801 (United States)

    2014-12-15

    Highlights: • A pulse device for a liquid lithium trench study is developed. • It consists of a coaxial plasma gun, a theta pinch, and guiding magnets. • A large energy enhancement is observed with the use of the plasma gun. • A further increase in energy and velocity is observed with the theta pinch. - Abstract: To simulate detrimental events in a tokamak and provide a test-stand for a liquid-lithium infused trench (LiMIT) device [1], a pulsed plasma source utilizing a theta pinch in conjunction with a coaxial plasma accelerator has been developed. The plasma is characterized using a triple Langmuir probe, optical methods, and a calorimeter. Clear advantages have been observed with the application of a coaxial plasma accelerator as a pre-ionization source. The experimental results of the plasma gun in conjunction with the existing theta pinch show a significant improvement from the previous energy deposition by a factor of 14 or higher, resulting in a maximum energy and heat flux of 0.065 ± 0.002 MJ/m{sup 2} and 0.43 ± 0.01 GW/m{sup 2}. A few ways to further increase the plasma heat flux for LiMIT experiments are discussed.

  14. High-capacity lithium-ion battery conversion cathodes based on iron fluoride nanowires and insights into the conversion mechanism.

    Science.gov (United States)

    Li, Linsen; Meng, Fei; Jin, Song

    2012-11-14

    The increasing demands from large-scale energy applications call for the development of lithium-ion battery (LIB) electrode materials with high energy density. Earth abundant conversion cathode material iron trifluoride (FeF(3)) has a high theoretical capacity (712 mAh g(-1)) and the potential to double the energy density of the current cathode material based on lithium cobalt oxide. Such promise has not been fulfilled due to the nonoptimal material properties and poor kinetics of the electrochemical conversion reactions. Here, we report for the first time a high-capacity LIB cathode that is based on networks of FeF(3) nanowires (NWs) made via an inexpensive and scalable synthesis. The FeF(3) NW cathode yielded a discharge capacity as high as 543 mAh g(-1) at the first cycle and retained a capacity of 223 mAh g(-1) after 50 cycles at room temperature under the current of 50 mA g(-1). Moreover, high-resolution transmission electron microscopy revealed the existence of continuous networks of Fe in the lithiated FeF(3) NWs after discharging, which is likely an important factor for the observed improved electrochemical performance. The loss of active material (FeF(3)) caused by the increasingly ineffective reconversion process during charging was found to be a major factor responsible for the capacity loss upon cycling. With the advantages of low cost, large quantity, and ease of processing, these FeF(3) NWs are not only promising battery cathode materials but also provide a convenient platform for fundamental studies and further improving conversion cathodes in general.

  15. A Core-Shell Fe/Fe2 O3 Nanowire as a High-Performance Anode Material for Lithium-Ion Batteries.

    Science.gov (United States)

    Na, Zhaolin; Huang, Gang; Liang, Fei; Yin, Dongming; Wang, Limin

    2016-08-16

    The preparation of novel one-dimensional core-shell Fe/Fe2 O3 nanowires as anodes for high-performance lithium-ion batteries (LIBs) is reported. The nanowires are prepared in a facile synthetic process in aqueous solution under ambient conditions with subsequent annealing treatment that could tune the capacity for lithium storage. When this hybrid is used as an anode material for LIBs, the outer Fe2 O3 shell can act as an electrochemically active material to store and release lithium ions, whereas the highly conductive and inactive Fe core functions as nothing more than an efficient electrical conducting pathway and a remarkable buffer to tolerate volume changes of the electrode materials during the insertion and extraction of lithium ions. The core-shell Fe/Fe2 O3 nanowire maintains an excellent reversible capacity of over 767 mA h g(-1) at 500 mA g(-1) after 200 cycles with a high average Coulombic efficiency of 98.6 %. Even at 2000 mA g(-1) , a stable capacity as high as 538 mA h g(-1) could be obtained. The unique composition and nanostructure of this electrode material contribute to this enhanced electrochemical performance. Due to the ease of large-scale fabrication and superior electrochemical performance, these hybrid nanowires are promising anode materials for the next generation of high-performance LIBs.

  16. Peapod-like Li3 VO4 /N-Doped Carbon Nanowires with Pseudocapacitive Properties as Advanced Materials for High-Energy Lithium-Ion Capacitors.

    Science.gov (United States)

    Shen, Laifa; Lv, Haifeng; Chen, Shuangqiang; Kopold, Peter; van Aken, Peter A; Wu, Xiaojun; Maier, Joachim; Yu, Yan

    2017-07-01

    Lithium ion capacitors are new energy storage devices combining the complementary features of both electric double-layer capacitors and lithium ion batteries. A key limitation to this technology is the kinetic imbalance between the Faradaic insertion electrode and capacitive electrode. Here, we demonstrate that the Li3 VO4 with low Li-ion insertion voltage and fast kinetics can be favorably used for lithium ion capacitors. N-doped carbon-encapsulated Li3 VO4 nanowires are synthesized through a morphology-inheritance route, displaying a low insertion voltage between 0.2 and 1.0 V, a high reversible capacity of ≈400 mAh g(-1) at 0.1 A g(-1) , excellent rate capability, and long-term cycling stability. Benefiting from the small nanoparticles, low energy diffusion barrier and highly localized charge-transfer, the Li3 VO4 /N-doped carbon nanowires exhibit a high-rate pseudocapacitive behavior. A lithium ion capacitor device based on these Li3 VO4 /N-doped carbon nanowires delivers a high energy density of 136.4 Wh kg(-1) at a power density of 532 W kg(-1) , revealing the potential for application in high-performance and long life energy storage devices. © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  17. Spongelike Nanosized Mn 3 O 4 as a High-Capacity Anode Material for Rechargeable Lithium Batteries

    KAUST Repository

    Gao, Jie

    2011-07-12

    Mn3O4 has been investigated as a high-capacity anode material for rechargeable lithium ion batteries. Spongelike nanosized Mn 3O4 was synthesized by a simple precipitation method and characterized by powder X-ray diffraction, Raman scattering and scanning electron microscopy. Its electrochemical performance, as an anode material, was evaluated by galvanostatic discharge-charge tests. The results indicate that this novel type of nanosized Mn3O4 exhibits a high initial reversible capacity (869 mA h/g) and significantly enhanced first Coulomb efficiency with a stabilized reversible capacity of around 800 mA h/g after over 40 charge/discharge cycles. © 2011 American Chemical Society.

  18. Multifunctional Free-Standing Gel Polymer Electrolyte with Carbon Nanofiber Interlayers for High-Performance Lithium-Sulfur Batteries.

    Science.gov (United States)

    Choi, Sinho; Song, Jianjun; Wang, Chengyin; Park, Soojin; Wang, Guoxiu

    2017-07-04

    Free-standing trimethylolpropane ethoxylate triacrylate gel polymer electrolyte is synthesized by a chemical cross-linking process and used as an electrolyte and separator membrane in lithium-sulfur batteries. The cross linked gel polymer electrolyte also exhibited a stable geometric size retention of 95 % at the high temperature of 130 °C. The as-prepared gel polymer electrolyte membrane with carbon nanofibers interlayer can effectively prevent polysulfide dissolution and shuttle effect, leading to significantly enhanced electrochemical properties, including high capacity and cycling stability, with an enhanced specific capacity of 790 mA h g(-1) after 100 cycles. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  19. Porous LiFePO4/C microspheres as high-power cathode materials for lithium ion batteries.

    Science.gov (United States)

    Sun, Bing; Wang, Ying; Wang, Bei; Kim, Hyun-Soo; Kim, Woo-Seong; Wang, Guoxiu

    2013-05-01

    Porous LiFePO4/C microspheres were synthesized by a novel hydrothermal reaction combined with high-temperature calcinations. The morphology of the prepared material was investigated by field-emission scanning electron microscopy. Porous microspheres with diameters around 1-3 microm were obtained, which consisting of primary LiFePO4 nanoparticles. The electrochemical performances of the as-prepared LiFePO4 microspheres were evaluated by cyclic voltammetry, electrochemical impedance spectroscopy and galvanostatic charge-discharge cycling. The carbon coated LiFePO4 microspheres showed lower polarization, higher rate capability, and better cycling stability than that of pristine LiFePO4 microspheres, indicating the potential application as the cathode material for high-power lithium ion batteries.

  20. Investigation of Metal Oxide/Carbon Nano Material as Anode for High Capacity Lithium-ion Cells

    Science.gov (United States)

    Wu, James Jianjun; Hong, Haiping

    2014-01-01

    NASA is developing high specific energy and high specific capacity lithium-ion battery (LIB) technology for future NASA missions. Current state-of-art LIBs have issues in terms of safety and thermal stability, and are reaching limits in specific energy capability based on the electrochemical materials selected. For example, the graphite anode has a limited capability to store Li since the theoretical capacity of graphite is 372 mAh/g. To achieve higher specific capacity and energy density, and to improve safety for current LIBs, alternative advanced anode, cathode, and electrolyte materials are pursued under the NASA Advanced Space Power System Project. In this study, the nanostructed metal oxide, such as Fe2O3 on carbon nanotubes (CNT) composite as an LIB anode has been investigated.

  1. Binders and Hosts for High-Capacity Lithium-ion Battery Anodes

    Science.gov (United States)

    Dufficy, Martin Kyle

    Lithium-ion batteries (LIBs) are universal electrochemical energy storage devices that have revolutionized our mobile society. Nonetheless, societal and technological advances drive consumer demand for LIBs with enhanced electrochemical performance, such as higher charge capacity and longer life, compared to conventional LIBs. One method to enhance LIB performance is to replace graphite, the industry standard anode since commercialization of LIBs in 1991, with high-charge capacity materials. Implementing high-capacity anode materials such as tin, silicon, and manganese vanadates, to LIBs presents challenges; Li-insertion is destructive to anode framework, and increasing capacity increases structural strains that pulverize anode materials and results in a short-cycle life. This thesis reports on various methods to extended the cycle life of high-capacity materials. Most of the work is conducted on nano-sized anode materials to reduce Li and electron transport pathway length (facilitating charge-transfer) and reduce strains from volume expansions (preserving anode structure). The first method involves encapsulating tin particles into a graphene-containing carbon nanofiber (CNF) matrix. The composite-CNF matrix houses tin particles to assume strains from tin-volume expansions and produces favorable surface-electrolyte chemistries for stable charge-discharge cycling. Before tin addition, graphene-containing CNFs are produced and assessed as anode materials for LIBs. Graphene addition to CNFs improves electronic and mechanical properties of CNFs. Furthermore, the 2-D nature of graphene provides Li-binding sites to enhance composite-CNF both first-cycle and high-rate capacities > 150% when compared to CNFs in the absence of graphene. With addition of Sn, we vary loadings and thermal production temperature to elucidate structure-composition relationships of tin and graphene-containing CNF electrodes that lead to increased capacity retention. Of note, electrodes containing

  2. Sulfur-graphene nanostructured cathodes via ball-milling for high-performance lithium-sulfur batteries.

    Science.gov (United States)

    Xu, Jiantie; Shui, Jianglan; Wang, Jianli; Wang, Min; Liu, Hua-Kun; Dou, Shi Xue; Jeon, In-Yup; Seo, Jeong-Min; Baek, Jong-Beom; Dai, Liming

    2014-10-28

    Although much progress has been made to develop high-performance lithium-sulfur batteries (LSBs), the reported physical or chemical routes to sulfur cathode materials are often multistep/complex and even involve environmentally hazardous reagents, and hence are infeasible for mass production. Here, we report a simple ball-milling technique to combine both the physical and chemical routes into a one-step process for low-cost, scalable, and eco-friendly production of graphene nanoplatelets (GnPs) edge-functionalized with sulfur (S-GnPs) as highly efficient LSB cathode materials of practical significance. LSBs based on the S-GnP cathode materials, produced by ball-milling 70 wt % sulfur and 30 wt % graphite, delivered a high initial reversible capacity of 1265.3 mAh g(-1) at 0.1 C in the voltage range of 1.5-3.0 V with an excellent rate capability, followed by a high reversible capacity of 966.1 mAh g(-1) at 2 C with a low capacity decay rate of 0.099% per cycle over 500 cycles, outperformed the current state-of-the-art cathode materials for LSBs. The observed excellent electrochemical performance can be attributed to a 3D "sandwich-like" structure of S-GnPs with an enhanced ionic conductivity and lithium insertion/extraction capacity during the discharge-charge process. Furthermore, a low-cost porous carbon paper pyrolyzed from common filter paper was inserted between the 0.7S-0.3GnP electrode and porous polypropylene film separator to reduce/eliminate the dissolution of physically adsorbed polysulfide into the electrolyte and subsequent cross-deposition on the anode, leading to further improved capacity and cycling stability.

  3. [Lithium nephropathy].

    Science.gov (United States)

    Kaczmarczyk, Ireneusz; Sułowicz, Władysław

    2013-01-01

    Lithium salts are the first-line drug therapy in the treatment of uni- and bipolar disorder since the sixties of the twentieth century. In the mid-70s, the first information about their nephrotoxicity appeared. Lithium salts have a narrow therapeutic index. Side effects during treatment are polyuria, polydipsia and nephrogenic diabetes insipidus. Accidental intoxication can cause acute renal failure requiring renal replacement therapy while receiving long-term lithium salt can lead to the development of chronic kidney disease. The renal biopsy changes revealed a type of chronic tubulointerstitial nephropathy. The imaging studies revealed the presence of numerous symmetric microcysts. Care of the patient receiving lithium should include regular determination of serum creatinine, creatinine clearance and monitoring of urine volume. In case of deterioration of renal function reducing the dose should be considered.

  4. Facile, mild and fast thermal-decomposition reduction of graphene oxide in air and its application in high-performance lithium batteries.

    Science.gov (United States)

    Wang, Zhong-li; Xu, Dan; Huang, Yun; Wu, Zhong; Wang, Li-min; Zhang, Xin-bo

    2012-01-25

    We firstly propose a facile, mild and effective thermal-decomposition strategy to prepare high-quality graphene at a low temperature of 300 °C in only 5 min under an ambient atmosphere. Applying the advantage of this strategy that provides an oxidizing atmosphere, pure V(2)O(5)/graphene composite is successfully synthesized and exerts excellent lithium storage properties.

  5. SnO2@TiO2 double-shell nanotubes for a lithium ion battery anode with excellent high rate cyclability.

    Science.gov (United States)

    Jeun, Jeong-Hoon; Park, Kyu-Young; Kim, Dai-Hong; Kim, Won-Sik; Kim, Hong-Chan; Lee, Byoung-Sun; Kim, Honggu; Yu, Woong-Ryeol; Kang, Kisuk; Hong, Seong-Hyeon

    2013-09-21

    SnO2@TiO2 double-shell nanotubes have been facilely synthesized by atomic layer deposition (ALD) using electrospun PAN nanofibers as templates. The double-shell nanotubes exhibited excellent high rate cyclability for lithium ion batteries. The retention of hollow structures during cycling was demonstrated.

  6. Carbon-Coated Fe3O4/VOx Hollow Microboxes Derived from Metal-Organic Frameworks as a High-Performance Anode Material for Lithium-Ion Batteries.

    Science.gov (United States)

    Zhao, Zhi-Wei; Wen, Tao; Liang, Kuang; Jiang, Yi-Fan; Zhou, Xiao; Shen, Cong-Cong; Xu, An-Wu

    2017-02-01

    As the ever-growing demand for high-performance power sources, lithium-ion batteries with high storage capacities and outstanding rate performance have been widely considered as a promising storage device. In this work, starting with metal-organic frameworks, we have developed a facile approach to the synthesis of hybrid Fe3O4/VOx hollow microboxes via the process of hydrolysis and ion exchange and subsequent calcination. In the constructed architecture, the hollow structure provides an efficient lithium ion diffusion pathway and extra space to accommodate the volume expansion during the insertion and extraction of Li(+). With the assistance of carbon coating, the obtained Fe3O4/VOx@C microboxes exhibit excellent cyclability and enhanced rate performance when employed as an anode material for lithium-ion batteries. As a result, the obtained Fe3O4/VOx@C delivers a high Coulombic efficiency (near 100%) and outstanding reversible specific capacity of 742 mAh g(-1) after 400 cycles at a current density of 0.5 A g(-1). Moreover, a remarkable reversible capacity of 556 mAh g(-1) could be retained even at a current density of 2 A g(-1). This study provides a fundamental understanding for the rational design of other composite oxides as high-performance electrode materials for lithium-ion batteries.

  7. High Lithium Capacity MxV 2O 5Ay· nH 2O for Rechargeable Batteries

    Science.gov (United States)

    Torardi, C. C.; Miao, C. R.; Lewittes, M. E.; Li, Z.

    2002-01-01

    The aqueous synthesis and electrochemical properties of nanocrystalline MxV2O5Ay·nH2O are described. It is easily and quickly prepared by precipitation from acidified vanadate solutions. MxV2O5Ay·nH2O has been characterized by X-ray powder diffraction, electron microscopy, TGA, chemical analyses, and electrochemical studies. The atomic structure is related to that of xerogel-derived V2O5·nH2O. In MxV2O5Ay·nH2O, M is a cation from the starting vanadate salt and A is an anion from the mineral acid. This material exhibits high, reversible Li capacity and may be considered for use in a cathode in primary and secondary batteries. The lithium capacity of an electrode composed of MxV2O5Ay·nH2O/EPDM/carbon (88/4/8) is ∼380(mA h)/g (C/80 rate) and the energy density is ∼1000(W h)/kg (120-μm-thick cathode, 4-1.5 V, versus Li metal anode). Critical parameters identified in the synthesis of MxV2O5Ay·nH2O, with respect to achieving high Li-ion insertion capacity, are acid/vanadium ratio, starting vanadate salt, and temperature. Inclusion of carbon black in the synthesis yields a composite that maintains the high Li capacity, lowers the electrochemical-cell polarization, and preserves the lithium capacity at higher discharge rates. Li-ion coin cells, using pre-lithiated graphite anodes, exhibit electrochemical performance comparable to that of Li-metal coin cells.

  8. Valve inlet fluid conditions for pressurizer safety and relief valves for B and W 177-FA and 205-FA plants. Final report. [PWR

    Energy Technology Data Exchange (ETDEWEB)

    Cartin, L.R.; Winks, R.W.; Merchent, J.W.; Brandt, R.T.

    1982-12-01

    The overpressurization transients for the Babcock and Wilcox Company's 177- and 205-FA units are reviewed to determine the range of fluid conditions expected at the inlet of pressurizer safety and relief valves. The final Safety Analysis Report, extended high-pressure injection, and cold overpressurization events are considered. The results of this review, presented in the form of tables and graphs, provide input to the PWR utilities in their justification that the fluid conditions under which their valve designs were tested as part of the EPRI PWR Safety and Relief Valve Test Program are representative of those expected in their unit(s).

  9. Research on Power Ramp Testing Method for PWR Fuel Rod at Research Reactor

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    In order to develop high performance fuel assembly for domestic nuclear power plant, it is necessary to master some fundamental test technology. So the research on the power ramp testing methods is proposed. A tentative power ramp test for short PWR fuel rod has been conducted at the heavy water research reactor (HWRR) in China Institute of Atomic Energy (CIAE) in May of 2001. The in-pile test rig was placed into the central channel of the reactor . The test rig consists of pressure pipe assembly, thimble, solid neutron absorbing screen and its driving parts, etc.. The test

  10. Evaluation of PWR and BWR pin cell benchmark results

    Energy Technology Data Exchange (ETDEWEB)

    Pijlgroms, B.J.; Gruppelaar, H.; Janssen, A.J. (Netherlands Energy Research Foundation (ECN), Petten (Netherlands)); Hoogenboom, J.E.; Leege, P.F.A. de (Interuniversitair Reactor Inst., Delft (Netherlands)); Voet, J. van der (Gemeenschappelijke Kernenergiecentrale Nederland NV, Dodewaard (Netherlands)); Verhagen, F.C.M. (Keuring van Electrotechnische Materialen NV, Arnhem (Netherlands))

    1991-12-01

    Benchmark results of the Dutch PINK working group on PWR and BWR pin cell calculational benchmark as defined by EPRI are presented and evaluated. The observed discrepancies are problem dependent: a part of the results is satisfactory, some other results require further analysis. A brief overview is given of the different code packages used in this analysis. (author). 14 refs., 9 figs., 30 tabs.

  11. Studies of a small PWR for onsite industrial power

    Energy Technology Data Exchange (ETDEWEB)

    Klepper, O.H.; Smith, W.R.

    1977-04-19

    Information on the use of a 300 to 400 MW(t) PWR type reactor for industrial applications is presented concerning the potential market, reliability considerations, reactor plant description, construction techniques, comparison between nuclear and fossil-fired process steam costs, alternative fossil-fired steam supplies, and industrial application.

  12. PACTEL and PWR PACTEL Test Facilities for Versatile LWR Applications

    Directory of Open Access Journals (Sweden)

    Virpi Kouhia

    2012-01-01

    Full Text Available This paper describes construction and experimental research activities with two test facilities, PACTEL and PWR PACTEL. The PACTEL facility, comprising of reactor pressure vessel parts, three loops with horizontal steam generators, a pressurizer, and emergency core cooling systems, was designed to model the thermal-hydraulic behaviour of VVER-440-type reactors. The facility has been utilized in miscellaneous applications and experiments, for example, in the OECD International Standard Problem ISP-33. PACTEL has been upgraded and modified on a case-by-case basis. The latest facility configuration, the PWR PACTEL facility, was constructed for research activities associated with the EPR-type reactor. A significant design basis is to utilize certain parts of PACTEL, and at the same time, to focus on a proper construction of two new loops and vertical steam generators with an extensive instrumentation. The PWR PACTEL benchmark exercise was launched in 2010 with a small break loss-of-coolant accident test as the chosen transient. Both facilities, PACTEL and PWR PACTEL, are maintained fully operational side by side.

  13. A neutronic study of the cycle PWR-CANDU

    Energy Technology Data Exchange (ETDEWEB)

    Silva, Alberto da; Pereira, Claubia; Veloso, Maria Auxiliadora Fortini; Fortini, Angela; Pinheiro, Ricardo Brant [Universidade Federal de Minas Gerais (UFMG), Belo Horizonte, MG (Brazil). Dept. de Engenharia Nuclear]. E-mail: albertomoc@terra.com.br; claubia@nuclear.ufmg.br; dora@nuclear.ufmg.br; fortini@nuclear.ufmg.br; rbp@nuclear.ufmg.br

    2007-07-01

    The cycle PWR-CANDU was simulated using the WIMSD-5B and ORIGEN2.1 codes. It was simulated a fuel burnup of 33,000 MWd/t for UO{sub 2} with enrichment of 3.2% and a fuel extended burnup of 45,000 MWd/t for UO{sub 2} with enrichments of 3.5%, 4.0% and 5.0% in a PWR reactor. The PWR discharged fuel was submitted to the simulation of deposition for five years. After that, it was submitted to AYROX reprocessing and used to produce a fuel to CANDU reactor. Then, it was simulated the burnup in the CANDU. Parameters such as infinite medium multiplication factor, k{sub inf}, fuel temperature coefficient of reactivity, {alpha}{sub TF}, moderator temperature coefficient of reactivity, {alpha}{sub TM}, the ratio rapid flux/total flux and the isotopic composition in the begin and the end of life were evaluated. The results showed that the fuels analyzed could be used on PWR and CANDU reactors without the need of change on the design of these reactors. (author)

  14. Methodology for the LABIHS PWR simulator modernization

    Energy Technology Data Exchange (ETDEWEB)

    Jaime, Guilherme D.G.; Oliveira, Mauro V., E-mail: gdjaime@ien.gov.b, E-mail: mvitor@ien.gov.b [Instituto de Engenharia Nuclear (IEN/CNEN-RJ), Rio de Janeiro, RJ (Brazil)

    2011-07-01

    The Human-System Interface Laboratory (LABIHS) simulator is composed by a set of advanced hardware and software components whose goal is to simulate the main characteristics of a Pressured Water Reactor (PWR). This simulator serves for a set of purposes, such as: control room modernization projects; designing of operator aiding systems; providing technological expertise for graphical user interfaces (GUIs) designing; control rooms and interfaces evaluations considering both ergonomics and human factors aspects; interaction analysis between operators and the various systems operated by them; and human reliability analysis in scenarios considering simulated accidents and normal operation. The simulator runs in a PA-RISC architecture server (HPC3700), developed nearby 2000's, using the HP-UX operating system. All mathematical modeling components were written using the HP Fortran-77 programming language with a shared memory to exchange data from/to all simulator modules. Although this hardware/software framework has been discontinued in 2008, with costumer support ceasing in 2013, it is still used to run and operate the simulator. Due to the fact that the simulator is based on an obsolete and proprietary appliance, the laboratory is subject to efficiency and availability issues, such as: downtime caused by hardware failures; inability to run experiments on modern and well known architectures; and lack of choice of running multiple simulation instances simultaneously. This way, there is a need for a proposal and implementation of solutions so that: the simulator can be ported to the Linux operating system, running on the x86 instruction set architecture (i.e. personal computers); we can simultaneously run multiple instances of the simulator; and the operator terminals run remotely. This paper deals with the design stage of the simulator modernization, in which it is performed a thorough inspection of the hardware and software currently in operation. Our goal is to

  15. Development and characterization of a high capacity lithium/thionyl chloride battery

    Science.gov (United States)

    Boyle, Gerald H.; Goebel, Franz

    A 30 V lithium/thionyl chloride battery with 320 Ah capacity capable of operating at currents of 14 to 75 A has been developed and tested over a temperature range from 15 to 71 °C. The 81 lb battery consists of nine series connected cylindrical cells in a three-by-three arrangement within an aluminum case. The cells are of a parallel disc electrode design with a total active surface area of 10 200 cm 2. Cells and batteries have each been tested for safety, performance and to a space environment. The battery has clearly performed in excess of the specification requirements. The cell design is very adaptable to many battery design requirements.

  16. Development and characterization of a high capacity lithium/thionyl chloride battery

    Energy Technology Data Exchange (ETDEWEB)

    Boyle, G.H. [Yardney Technical Products, Inc., Pawcatuck, CT (United States); Goebel, F. [Yardney Technical Products, Inc., Pawcatuck, CT (United States)

    1995-04-01

    A 30 V lithium/thionyl chloride battery with 320 Ah capacity capable of operating at currents of 14 to 75 A has been developed and tested over a temperature range from 15 to 71 C. The 81 lb battery consists of nine series connected cylindrical cells in a three-by-three arrangement within an aluminum case. The cells are of a parallel disc electrode design with a total active surface area of 10 200 cm{sup 2}. Cells and batteries have each been tested for safety, performance and to a space environment. The battery has clearly performed in excess of the specification requirements. The cell design is very adaptable to many battery design requirements. (orig.)

  17. A High Voltage Olivine Cathode for Application in Lithium-Ion Batteries.

    Science.gov (United States)

    Di Lecce, Daniele; Brescia, Rosaria; Scarpellini, Alice; Prato, Mirko; Hassoun, Jusef

    2016-01-01

    A new olivine composition (i.e., LiFe0.25 Mn0.5 Co0.25 PO4) is proposed as electrode material with increased energy density for application in lithium-ion batteries. The new formulation increases the working voltage and induces different electrochemical behavior with respect to bare olivine materials based on Fe. The study provides deep insight into the features of the Fe(3+) /Fe(2+), Mn(3+)/Mn(2+), and Co(3+)/Co(2+) redox couples within the olivine lattice in terms of electrochemical activity, Li(+) transport properties, and Li-cell behavior. The electrochemical characterization clearly reveals the voltage signatures corresponding to the various metals; however, the Mn(3+)/Mn(2+) process has higher intrinsic polarization with respect to Fe(3+)/Fe(2+) and Co(3+)/Co(2+). This issue is efficiently mitigated by carbon coating the material, resulting in enhanced electrochemical performances.

  18. Pitting corrosion transformation of SUS304 stainless steel in lithium bromide solution at high temperature

    Energy Technology Data Exchange (ETDEWEB)

    Chen, H.X.; Ma, X.H.; Chen, J.B.; Bo, S.S. [Institute of Chemical Engineering, Dalian University of Technology, Dalian (China)

    2009-05-15

    The foundational data and rules of SUS304 corrosion in aqueous lithium bromide solution at 150-200 C have been investigated by means of weight loss in this paper. The Taguchi method was chosen to investigate the effects of variables on corrosion at higher temperature. Concentration of dissolved oxygen was controlled by keeping the vessel pressure at 1.3 kPa (absolute) before the experiment. The results showed that there was a transformation tendency from pitting corrosion to general corrosion and transition concentration of pitting and film corrosion decreased with increase in solution temperature. The adsorption, activity, and diffusivity of bromine ion led to different corrosion modalities. (Abstract Copyright [2009], Wiley Periodicals, Inc.)

  19. Functionalized graphene-based cathode for highly reversible lithium-sulfur batteries.

    Science.gov (United States)

    Kim, Jin Won; Ocon, Joey D; Park, Dong-Won; Lee, Jaeyoung

    2014-05-01

    In this article, we highlight the salient issues in the development of lithium-sulfur battery (LSB) cathodes, present different points of view in solving them, and argue, why in the future, functionalized graphene or graphene oxide might be the ultimate solution towards LSB commercialization. As shown by previous studies and also in our recent work, functionalized graphene and graphene oxide enhance the reversibility of the charge-discharge process by trapping polysulfides in the oxygen functional groups on the graphene surface, thus minimizing polysulfide dissolution. This will be helpful for the rational design of new cathode structures based on graphene for LSBs with minimal capacity fading, low extra cost, and without the unnecessary weight increase caused by metal/metal oxide additives.

  20. High-energy density nonaqueous all redox flow lithium battery enabled with a polymeric membrane.

    Science.gov (United States)

    Jia, Chuankun; Pan, Feng; Zhu, Yun Guang; Huang, Qizhao; Lu, Li; Wang, Qing

    2015-11-01

    Redox flow batteries (RFBs) are considered one of the most promising large-scale energy storage technologies. However, conventional RFBs suffer from low energy density due to the low solubility of the active materials in electrolyte. On the basis of the redox targeting reactions of battery materials, the redox flow lithium battery (RFLB) demonstrated in this report presents a disruptive approach to drastically enhancing the energy density of flow batteries. With LiFePO4 and TiO2 as the cathodic and anodic Li storage materials, respectively, the tank energy density of RFLB could reach ~500 watt-hours per liter (50% porosity), which is 10 times higher than that of a vanadium redox flow battery. The cell exhibits good electrochemical performance under a prolonged cycling test. Our prototype RFLB full cell paves the way toward the development of a new generation of flow batteries for large-scale energy storage.

  1. Hybrid microfiber-lithium-niobate nanowaveguide structures as high-purity heralded single-photon sources

    Science.gov (United States)

    Main, Philip; Mosley, Peter J.; Ding, Wei; Zhang, Lijian; Gorbach, Andrey V.

    2016-12-01

    We propose a compact, fiber-integrated architecture for photon-pair generation by parametric downconversion with unprecedented flexibility in the properties of the photons produced. Our approach is based on a thin-film lithium niobate nanowaveguide, evanescently coupled to a tapered silica microfiber. We demonstrate how controllable mode hybridization between the fiber and waveguide yields control over the joint spectrum of the photon pairs. We also investigate how independent engineering of the linear and nonlinear properties of the structure can be achieved through the addition of a tapered, proton-exchanged layer to the waveguide. This allows further refinement of the joint spectrum through custom profiling of the effective nonlinearity, drastically improving the purity of the heralded photons. We give details of a source design capable of generating heralded single photons in the telecom wavelength range with purity of at least 0.95, and we provide a feasible fabrication methodology.

  2. Performance Model for High-Power Lithium Titanate Oxide Batteries based on Extended Characterization Tests

    DEFF Research Database (Denmark)

    Stroe, Ana-Irina; Swierczynski, Maciej Jozef; Stroe, Daniel Ioan

    2015-01-01

    Lithium-ion (Li-ion) batteries are found nowadays not only in portable/consumer electronics but also in more power demanding applications, such as stationary renewable energy storage, automotive and back-up power supply, because of their superior characteristics in comparison to other energy...... storage technologies. Nevertheless, prior to be used in any of the aforementioned application, a Li-ion battery cell must be intensively characterized and its behavior needs to be understood. This can be realized by performing extended laboratory characterization tests and developing Li-ion battery...... performance models. Furthermore, accurate performance models are necessary in order to analyze the behavior of the battery cell under different mission profiles, by simulation; thus, avoiding time and cost demanding real life tests. This paper presents the development and the parametrization of a performance...

  3. Promise and reality of post-lithium-ion batteries with high energy densities

    Science.gov (United States)

    Choi, Jang Wook; Aurbach, Doron

    2016-04-01

    Energy density is the main property of rechargeable batteries that has driven the entire technology forward in past decades. Lithium-ion batteries (LIBs) now surpass other, previously competitive battery types (for example, lead-acid and nickel metal hydride) but still require extensive further improvement to, in particular, extend the operation hours of mobile IT devices and the driving mileages of all-electric vehicles. In this Review, we present a critical overview of a wide range of post-LIB materials and systems that could have a pivotal role in meeting such demands. We divide battery systems into two categories: near-term and long-term technologies. To provide a realistic and balanced perspective, we describe the operating principles and remaining issues of each post-LIB technology, and also evaluate these materials under commercial cell configurations.

  4. Highly conductive freestanding graphene films as anode current collectors for flexible lithium-ion batteries.

    Science.gov (United States)

    Rana, Kuldeep; Singh, Jyoti; Lee, Jeong-Taik; Park, Jong Hyeok; Ahn, Jong-Hyun

    2014-07-23

    The electrodes in lithium-ion batteries (LIBs) are typically films that are arranged on metal foil current collectors with a thickness of several tens of μm. Here, we report on the preparation of a thick free-standing graphene film synthesized by CVD as an alternative to Cu foil as an anode current collector. As a model system, MoS2 anodes with a flower-like morphology were anchored onto the surface of the thick graphene film. A hybrid and binder free anode without a conventional metal current collector exhibited an excellent capacity value of around 580 mAh/g (@50 mA/g) and reasonable charge/discharge cyclability. The work presented here may stimulate the use of graphene films as replacements for conventional current collectors and additive free electrode in LIBs.

  5. Strong Lithium Polysulfide Chemisorption on Electroactive Sites of Nitrogen-Doped Carbon Composites For High-Performance Lithium–Sulfur Battery Cathodes

    Energy Technology Data Exchange (ETDEWEB)

    Song, Jiangxuan; Gordin, Mikhail; Xu, Terrence; Chen, Shuru; Yu, Zhaoxin; Sohn, Hiesang; Lu, Jun; Ren, Yang; Duan, Yuhua; wang, Donghai

    2015-03-27

    Despite the high theoretical capacity of lithium–sulfur batteries, their practical applications are severely hindered by a fast capacity decay, stemming from the dissolution and diffusion of lithium polysulfides in the electrolyte. A novel functional carbon composite (carbon-nanotube-interpenetrated mesoporous nitrogen-doped carbon spheres, MNCS/CNT), which can strongly adsorb lithium polysulfides, is now reported to act as a sulfur host. The nitrogen functional groups of this composite enable the effective trapping of lithium polysulfides on electroactive sites within the cathode, leading to a much improved electrochemical performance (1200 mAh g-1 after 200 cycles). The enhancement in adsorption can be attributed to the chemical bonding of lithium ions by nitrogen functional groups in the MNCS/CNT framework. Furthermore, the micrometer-sized spherical structure of the material yields a high areal capacity (ca. 6 mAh cm-2) with a high sulfur loading of approximately 5 mg cm-2, which is ideal for practical applications of the lithium–sulfur batteries.

  6. Removing hydrochloric acid exhaust products from high performance solid rocket propellant using aluminum-lithium alloy

    Energy Technology Data Exchange (ETDEWEB)

    Terry, Brandon C., E-mail: terry13@purdue.edu [School of Aeronautics and Astronautics, Purdue University, Zucrow Laboratories, 500 Allison Rd, West Lafayette, IN 47907 (United States); Sippel, Travis R. [Department of Mechanical Engineering, Iowa State University, 2025 Black Engineering, Ames, IA 50011 (United States); Pfeil, Mark A. [School of Aeronautics and Astronautics, Purdue University, Zucrow Laboratories, 500 Allison Rd, West Lafayette, IN 47907 (United States); Gunduz, I.Emre; Son, Steven F. [School of Mechanical Engineering, Purdue University, Zucrow Laboratories, 500 Allison Rd, West Lafayette, IN 47907 (United States)

    2016-11-05

    Highlights: • Al-Li alloy propellant has increased ideal specific impulse over neat aluminum. • Al-Li alloy propellant has a near complete reduction in HCl acid formation. • Reduction in HCl was verified with wet bomb experiments and DSC/TGA-MS/FTIR. - Abstract: Hydrochloric acid (HCl) pollution from perchlorate based propellants is well known for both launch site contamination, as well as the possible ozone layer depletion effects. Past efforts in developing environmentally cleaner solid propellants by scavenging the chlorine ion have focused on replacing a portion of the chorine-containing oxidant (i.e., ammonium perchlorate) with an alkali metal nitrate. The alkali metal (e.g., Li or Na) in the nitrate reacts with the chlorine ion to form an alkali metal chloride (i.e., a salt instead of HCl). While this technique can potentially reduce HCl formation, it also results in reduced ideal specific impulse (I{sub SP}). Here, we show using thermochemical calculations that using aluminum-lithium (Al-Li) alloy can reduce HCl formation by more than 95% (with lithium contents ≥15 mass%) and increase the ideal I{sub SP} by ∼7 s compared to neat aluminum (using 80/20 mass% Al-Li alloy). Two solid propellants were formulated using 80/20 Al-Li alloy or neat aluminum as fuel additives. The halide scavenging effect of Al-Li propellants was verified using wet bomb combustion experiments (75.5 ± 4.8% reduction in pH, ∝ [HCl], when compared to neat aluminum). Additionally, no measurable HCl evolution was detected using differential scanning calorimetry coupled with thermogravimetric analysis, mass spectrometry, and Fourier transform infrared absorption.

  7. A facile approach to make high performance nano-fiber reinforced composite separator for lithium ion batteries

    Science.gov (United States)

    Huang, Xiaosong

    2016-08-01

    The separator is a porous membrane located between the negative and the positive electrodes. In this work, a nano-fiber reinforced composite separator was developed. Compared with the commercial polyolefin separator, the composite separator showed superior (a) dimensional stability at elevated temperatures relative to conventional separators and (b) wettability by the liquid electrolyte. After being saturated with a commercial LiPF6-ethylene carbonate-dimethyl carbonate electrolyte, the composite separator enabled a high effective ionic conductivity (σeff) of 1.25 mS/cm. A stable cycle performance and an improved rate capability have been observed in the coin cells with the composite separator. This initial study shows that this type of composite membranes can be a promising alternative separator for lithium ion batteries.

  8. Preparation of Advanced Carbon Anode Materials from Mesocarbon Microbeads for Use in High C-Rate Lithium Ion Batteries

    Directory of Open Access Journals (Sweden)

    Ming-Dar Fang

    2015-06-01

    Full Text Available Mesophase soft carbon (MSC and mesophase graphite (SMG, for use in comparative studies of high C-rate Lithium Ion Battery (LIB anodes, were made by heating mesocarbon microbeads (MCMB at 1300 °C and 3000 °C; respectively. The crystalline structures and morphologies of the MSC, SMG, and commercial hard carbon (HC were investigated by X-ray diffraction, transmission electron microscopy, scanning electron microscopy, and Raman spectroscopy. Additionally, their electrochemical properties, when used as anode materials in LIBs, were also investigated. The results show that MSC has a superior charging rate capability compared to SMG and HC. This is attributed to MSC having a more extensive interlayer spacing than SMG, and a greater number of favorably-oriented pathways when compared to HC.

  9. Development of density-functional theory for a plasmon-assisted superconducting state: application to lithium under high pressures.

    Science.gov (United States)

    Akashi, Ryosuke; Arita, Ryotaro

    2013-08-02

    We extend the density-functional theory for superconductors (SCDFT) to take account of the dynamical structure of the screened Coulomb interaction. We construct an exchange-correlation kernel in the SCDFT gap equation on the basis of the random-phase approximation, where electronic collective excitations such as plasmons are properly treated. Through an application to fcc lithium under high pressures, we demonstrate that our new kernel gives higher transition temperatures (T(c)) when the plasmon and phonon cooperatively mediate pairing and it improves the agreement between the calculated and experimentally observed T(c). The present formalism opens the door to nonempirical studies on unconventional electron mechanisms of superconductivity based on density-functional theory.

  10. SU-8 photoresist-derived electrospun carbon nanofibres as high-capacity anode material for lithium ion battery

    Indian Academy of Sciences (India)

    M KAKUNURI; S KAUSHIK; A SAINI; C S SHARMA

    2017-06-01

    A binder-free carbon nanofibres web over stainless-steel wafer current collector was fabricated by controlled pyrolysis of electrospun SU-8 photoresist nanofibres. Electrochemical performance of the as-prepared carbon nanofibresweb was investigated by performing charge–discharge experiments at different current densities. At low current density (37.2 mA g$^{−1}, 0.1$C$), SU-8-derived carbon nanofabric showed a large initial discharge capacity (1417 mAh g$^{−1}$) with sufficiently higher initial coulombic efficiency ($\\sim$55%). More importantly, this carbon nanofibres web also exhibited excellent rate performance with considerably higher specific capacities at higher current densities (358 mAh g$^{−1}$ at 1C). This superior electrochemical performance, in particular at high current rates, can be attributed to small lithium ion diffusion length andresilience in entangled carbon nanofibres to accommodate volume changes during charging and discharging.

  11. A chemistry and material perspective on lithium redox flow batteries towards high-density electrical energy storage.

    Science.gov (United States)

    Zhao, Yu; Ding, Yu; Li, Yutao; Peng, Lele; Byon, Hye Ryung; Goodenough, John B; Yu, Guihua

    2015-11-21

    Electrical energy storage system such as secondary batteries is the principle power source for portable electronics, electric vehicles and stationary energy storage. As an emerging battery technology, Li-redox flow batteries inherit the advantageous features of modular design of conventional redox flow batteries and high voltage and energy efficiency of Li-ion batteries, showing great promise as efficient electrical energy storage system in transportation, commercial, and residential applications. The chemistry of lithium redox flow batteries with aqueous or non-aqueous electrolyte enables widened electrochemical potential window thus may provide much greater energy density and efficiency than conventional redox flow batteries based on proton chemistry. This Review summarizes the design rationale, fundamentals and characterization of Li-redox flow batteries from a chemistry and material perspective, with particular emphasis on the new chemistries and materials. The latest advances and associated challenges/opportunities are comprehensively discussed.

  12. Direct first-principles simulation of a high-performance electron emitter: Lithium-oxide-coated diamond surface

    Energy Technology Data Exchange (ETDEWEB)

    Miyamoto, Yoshiyuki, E-mail: yoshi-miyamoto@aist.go.jp; Miyazaki, Takehide [Nanosystem Research Institute, National Institute of Advanced Industrial Science and Technology (AIST), Central 2, 1-1-1 Umezono, Tsukuba, Ibaraki 305-8568 (Japan); Takeuchi, Daisuke; Yamasaki, Satoshi [Energy Technology Research Institute, National Institute of Advanced Industrial Science and Technology (AIST), Central 2, 1-1-1 Umezono, Tsukuba, Ibaraki 305-8568 (Japan); JST, ALCA, 4-1-8 Honcho, Kawaguchi, Saitama 332-0012 (Japan)

    2014-09-28

    We examined the field emission properties of lithium(Li)/oxygen(O)-co-terminated diamond (001) surface [C(001)-LiO] through real-time electron dynamics simulation under an applied field. The current emitted from this surface was found to be more than four-fold that emitted by an H-terminated (001) surface, the latter being a typical negative electron affinity system. This high performance is attributed to the Li layer, which bends the potential wall of O-induced electron pockets down in the direction of vacuum, thus facilitating electron emission. Detailed analysis of the emitted electrons and the profile of the self-consistent potential elucidated that the role of O atoms changes from an electron barrier on OH-terminated diamond surfaces to an outlet for electron emission on C(001)-LiO.

  13. A mild route to mesoporous Mo2C-C hybrid nanospheres for high performance lithium-ion batteries

    Science.gov (United States)

    Gao, Qing; Zhao, Xinyu; Xiao, Ying; Zhao, Di; Cao, Minhua

    2014-05-01

    In this work, we have developed a mild route to fabricate typically mesoporous Mo2C-C hybrid nanospheres based on a solvothermal synthesis and reduction-carbonization process. This work opens a low-temperature route to synthesize valuable carbides. The resultant Mo2C-C hybrid, for the first time, is used as an anode material in lithium ion batteries (LIBs). Compared with bulk Mo2C, the Mo2C-C hybrid exhibits much better electrochemical performance. Remarkably, the hybrid electrode can deliver a specific capacity of over 670 mA h g-1 after 50 cycles at 100 mA g-1, which is much higher than that of the bulk material (113 mA h g-1). Even cycled at a high current density of 1000 mA g-1, high capacities of around 400-470 mA h g-1 can still be retained for the Mo2C-C hybrid. It might benefit from the synergistic effect of the nanohybridization, effectively relieving the volume change during the repeated lithium insertion-extraction reactions and maintaining the integrity of the electrical connections. It is expected that the present synthesis strategy for the Mo2C-C hybrid can be extended to other nanostructured carbides with good energy storage performance.In this work, we have developed a mild route to fabricate typically mesoporous Mo2C-C hybrid nanospheres based on a solvothermal synthesis and reduction-carbonization process. This work opens a low-temperature route to synthesize valuable carbides. The resultant Mo2C-C hybrid, for the first time, is used as an anode material in lithium ion batteries (LIBs). Compared with bulk Mo2C, the Mo2C-C hybrid exhibits much better electrochemical performance. Remarkably, the hybrid electrode can deliver a specific capacity of over 670 mA h g-1 after 50 cycles at 100 mA g-1, which is much higher than that of the bulk material (113 mA h g-1). Even cycled at a high current density of 1000 mA g-1, high capacities of around 400-470 mA h g-1 can still be retained for the Mo2C-C hybrid. It might benefit from the synergistic effect of

  14. Facile mass production of nanoporous SnO2 nanosheets as anode materials for high performance lithium-ion batteries.

    Science.gov (United States)

    Wei, Wenli; Du, Pengcheng; Liu, Dong; Wang, Hongxing; Liu, Peng

    2017-10-01

    Facile one-step ultrasonic-assisted chemical precipitation strategy has been developed for the mass production of SnO2 nanomaterials with different morphologies. As anode material for lithium-ion batteries, the nanoporous SnO2 nanosheets exhibited an extremely high initial specific capacity of 2231mAh/g in comparison with 1242mAh/g of the SnO2 microcrystals and 1244mAh/g of the nanoporous SnO2 nanoflowers. Meanwhile the nanoporous SnO2 nanosheet electrode displayed a specific capacity of 688mAh/g after 60 cycles at 0.2 A/g current density and an extraordinary capacity retention of 224mAh/g at a current density of 8A/g (approximately 10 C) owing to a huge increase of Li(+) diffusion coefficient. Copyright © 2017 Elsevier Inc. All rights reserved.

  15. Solid solution lithium alloy cermet anodes

    Science.gov (United States)

    Richardson, Thomas J.

    2013-07-09

    A metal-ceramic composite ("cermet") has been produced by a chemical reaction between a lithium compound and another metal. The cermet has advantageous physical properties, high surface area relative to lithium metal or its alloys, and is easily formed into a desired shape. An example is the formation of a lithium-magnesium nitride cermet by reaction of lithium nitride with magnesium. The reaction results in magnesium nitride grains coated with a layer of lithium. The nitride is inert when used in a battery. It supports the metal in a high surface area form, while stabilizing the electrode with respect to dendrite formation. By using an excess of magnesium metal in the reaction process, a cermet of magnesium nitride is produced, coated with a lithium-magnesium alloy of any desired composition. This alloy inhibits dendrite formation by causing lithium deposited on its surface to diffuse under a chemical potential into the bulk of the alloy.

  16. Facile synthesis of novel tunable highly porous CuO nanorods for high rate lithium battery anodes with realized long cycle life and high reversible capacity.

    Science.gov (United States)

    Wang, Linlin; Gong, Huaxu; Wang, Caihua; Wang, Dake; Tang, Kaibin; Qian, Yitai

    2012-11-07

    Various CuO nanostructures have been well studied as anode materials for lithium ion batteries (LIBs); however, there are few reports on the synthesis of porous CuO nanostructures used for anode materials, especially one-dimensional (1D) porous CuO. In this work, novel 1D highly porous CuO nanorods with tunable porous size were synthesized in large-quantities by a new, friendly, but very simple approach. We found that the pore size could be controlled by adjusting the sintering temperature in the calcination process. With the rising of calcination temperature, the pore size of CuO has been tuned in the range of ∼0.4 nm to 22 nm. The porous CuO materials have been applied as anode materials in LIBs and the effects of porous size on the electrochemical properties were observed. The highly porous CuO nanorods with porous size in the range of ∼6 nm to 22 nm yielded excellent high specific capacity, good cycling stability, and high rate performance, superior to that of most reported CuO nanocomposites. The CuO material delivers a high reversible capacity of 654 mA h g(-1) and 93% capacity retention over 200 cycles at a rate of 0.5 C. It also exhibits excellent high rate capacity of 410 mA h g(-1) even at 6 C. These results suggest that the facile synthetic method of producing a tunable highly porous CuO nanostructure can realize a long cycle life with high reversible capacity, which is suitable for next-generation high-performance LIBs.

  17. Lithium-free transition metal monoxides for positive electrodes in lithium-ion batteries

    Science.gov (United States)

    Jung, Sung-Kyun; Kim, Hyunchul; Cho, Min Gee; Cho, Sung-Pyo; Lee, Byungju; Kim, Hyungsub; Park, Young-Uk; Hong, Jihyun; Park, Kyu-Young; Yoon, Gabin; Seong, Won Mo; Cho, Yongbeom; Oh, Myoung Hwan; Kim, Haegyeom; Gwon, Hyeokjo; Hwang, Insang; Hyeon, Taeghwan; Yoon, Won-Sub; Kang, Kisuk

    2017-01-01

    Lithium-ion batteries based on intercalation compounds have dominated the advanced portable energy storage market. The positive electrode materials in these batteries belong to a material group of lithium-conducting crystals that contain redox-active transition metal and lithium. Materials without lithium-conducting paths or lithium-free compounds could be rarely used as positive electrodes due to the incapability of reversible lithium intercalation or the necessity of using metallic lithium as negative electrodes. These constraints have significantly limited the choice of materials and retarded the development of new positive electrodes in lithium-ion batteries. Here, we demonstrate that lithium-free transition metal monoxides that do not contain lithium-conducting paths in their crystal structure can be converted into high-capacity positive electrodes in the electrochemical cell by initially decorating the monoxide surface with nanosized lithium fluoride. This unusual electrochemical behaviour is attributed to a surface conversion reaction mechanism in contrast with the classic lithium intercalation reaction. Our findings will offer a potential new path in the design of positive electrode materials in lithium-ion batteries.

  18. Advanced Micro/Nanostructures for Lithium Metal Anodes.

    Science.gov (United States)

    Zhang, Rui; Li, Nian-Wu; Cheng, Xin-Bing; Yin, Ya-Xia; Zhang, Qiang; Guo, Yu-Guo

    2017-03-01

    Owning to their very high theoretical capacity, lithium metal anodes are expected to fuel the extensive practical applications in portable electronics and electric vehicles. However, unstable solid electrolyte interphase and lithium dendrite growth during lithium plating/stripping induce poor safety, low Coulombic efficiency, and short span life of lithium metal batteries. Lately, varies of micro/nanostructured lithium metal anodes are proposed to address these issues in lithium metal batteries. With the unique surface, pore, and connecting structures of different nanomaterials, lithium plating/stripping processes have been regulated. Thus the electrochemical properties and lithium morphologies have been significantly improved. These micro/nanostructured lithium metal anodes shed new light on the future applications for lithium metal batteries.

  19. Cross-linked branching nanohybrid polymer electrolyte with monodispersed TiO2 nanoparticles for high performance lithium-ion batteries

    Science.gov (United States)

    Ma, Cheng; Zhang, Jinfang; Xu, Mingquan; Xia, Qingbing; Liu, Jiatu; Zhao, Shuai; Chen, Libao; Pan, Anqiang; Ivey, Douglas G.; Wei, Weifeng

    2016-06-01

    Nanohybrid polymer electrolytes (NHPE) with ceramic particles have attracted significant attention owing to their improvement in electrochemical performance. However, particle aggregation and weak nanoparticle/polymer matrix interaction restrict their further application in lithium-ion batteries (LIBs). We demonstrate a facile in-situ polymerization/crystallization method to synthesize a homogeneous TiO2-grafted NHPE with a cross-linked branching structure, comprised of ion-conducting poly(ethylene glycol) methyl ether methacrylate (PEGMEM) and non-polar stearyl methacrylate (SMA). This technique is different from existing methods of blending functionalized ceramic particles into the polymer matrix. Highly monodispersed TiO2 nanocrystals enhance the effective interfacial interactions between particles and polymer matrix, which suppress the crystallization of ethylene oxide (EO) groups and facilitate forming continuously interconnected ion-conducting channels. Moreover, an increased dissociation degree of Li salt can also be achieved. The TiO2-grafted NHPE exhibits superior electrochemical properties with an ionic conductivity of 1.1 × 10-4 S cm-1 at 30 °C, a high lithium ion transference number and excellent interfacial compatibility with the lithium electrode. In particular, a lithium-ion battery based on TiO2-grafted NHPE demonstrates good C-rate performance, as well as excellent cycling stability with an initial discharge capacity of 153.5 mAh g-1 and a capacity retention of 96% after 300 cycles at 1 C (80 °C).

  20. High power accelerator-based boron neutron capture with a liquid lithium target and new applications to treatment of infectious diseases

    Energy Technology Data Exchange (ETDEWEB)

    Halfon, S. [Soreq NRC, Yavne 81800 (Israel); Racah Institute of Physics, Hebrew University, Jerusalem 91904 (Israel)], E-mail: halfon@phys.huji.ac.il; Paul, M. [Racah Institute of Physics, Hebrew University, Jerusalem 91904 (Israel); Steinberg, D. [Biofilm Laboratory, Institute of Dental Sciences, Faculty of Dentistry, Hebrew University-Hadassah (Israel); Nagler, A.; Arenshtam, A.; Kijel, D. [Soreq NRC, Yavne 81800 (Israel); Polacheck, I. [Clinical Microbiology and Infectious Diseases, Hadassah-Hebrew University Medical Center (Israel); Srebnik, M. [Department of Medicinal Chemistry and Natural Products, School of Pharmacy, Hebrew University, Jerusalem 91120 (Israel)

    2009-07-15

    A new conceptual design for an accelerator-based boron neutron capture therapy (ABNCT) facility based on the high-current low-energy proton beam driven by the linear accelerator at SARAF (Soreq Applied Research Accelerator Facility) incident on a windowless forced-flow liquid-lithium target, is described. The liquid-lithium target, currently in construction at Soreq NRC, will produce a neutron field suitable for the BNCT treatment of deep-seated tumor tissues, through the reaction {sup 7}Li(p,n){sup 7}Be. The liquid-lithium target is designed to overcome the major problem of solid lithium targets, namely to sustain and dissipate the power deposited by the high-intensity proton beam. Together with diseases conventionally targeted by BNCT, we propose to study the application of our setup to a novel approach in treatment of diseases associated with bacterial infections and biofilms, e.g. inflammations on implants and prosthetic devices, cystic fibrosis, infectious kidney stones. Feasibility experiments evaluating the boron neutron capture effectiveness on bacteria annihilation are taking place at the Soreq nuclear reactor.