WorldWideScience

Sample records for anodic materials

  1. Anodic Materials for Electrocatalytic Ozone Generation

    OpenAIRE

    Yun-Hai Wang; Qing-Yun Chen

    2013-01-01

    Ozone has wide applications in various fields. Electrocatalytic ozone generation technology as an alternative method to produce ozone is attractive. Anodic materials have significant effect on the ozone generation efficiency. The research progress on anodic materials for electrocatalytic ozone generation including the cell configuration and mechanism is addressed in this review. The lead dioxide and nickel-antimony-doped tin dioxide anode materials are introduced in detail, including their st...

  2. New High-Energy Nanofiber Anode Materials

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Xiangwu; Fedkiw, Peter; Khan, Saad; Huang, Alex; Fan, Jiang

    2013-11-15

    The overall goal of the proposed work was to use electrospinning technology to integrate dissimilar materials (lithium alloy and carbon) into novel composite nanofiber anodes, which simultaneously had high energy density, reduced cost, and improved abuse tolerance. The nanofiber structure allowed the anodes to withstand repeated cycles of expansion and contraction. These composite nanofibers were electrospun into nonwoven fabrics with thickness of 50 μm or more, and then directly used as anodes in a lithium-ion battery. This eliminated the presence of non-active materials (e.g., conducting carbon black and polymer binder) and resulted in high energy and power densities. The nonwoven anode structure also provided a large electrode-electrolyte interface and, hence, high rate capacity and good lowtemperature performance capability. Following are detailed objectives for three proposed project periods. • During the first six months: Obtain anodes capable of initial specific capacities of 650 mAh/g and achieve ~50 full charge/discharge cycles in small laboratory scale cells (50 to 100 mAh) at the 1C rate with less than 20 percent capacity fade; • In the middle of project period: Assemble, cycle, and evaluate 18650 cells using proposed anode materials, and demonstrate practical and useful cycle life (750 cycles of ~70% state of charge swing with less than 20% capacity fade) in 18650 cells with at least twice improvement in the specific capacity than that of conventional graphite electrodes; • At the end of project period: Deliver 18650 cells containing proposed anode materials, and achieve specific capacities greater than 1200 mAh/g and cycle life longer than 5000 cycles of ~70% state of charge swing with less than 20% capacity fade.

  3. Materials characterization of cermet anodes tested in a pilot cell

    Energy Technology Data Exchange (ETDEWEB)

    Windisch, C.F. Jr.; Strachan, D.M.; Henager, C.H. Jr. (Pacific Northwest Lab., Richland, WA (United States)); Alcorn, T.R.; Tabereaux, A.T.; Richards, N.E. (Reynolds Metals Co., Muscle Shoals, AL (United States). Mfg. Technology Lab.)

    1993-02-01

    Cermet anodes were evaluated as nonconsumable substitutes for carbon anodes using a pilot-scale reduction cell at the Reynolds Manufacturing Technology Laboratory. After pilot cell testing, tile anodes were subjected to extensive materials characterization and physical properties measurements at the Pacific Northwest Laboratory. Significant changes in the composition of the cermet anodes were observed including the growth of a reaction layer and penetration of electrolyte deep into the cermet matrix. Fracture strength and toughness were measured as a function of temperature and the ductile-brittle transition wasreduced by 500C following pilot cell testing. These results imply difficulties with anode material and control of operating conditions in the pilot cell, and suggest that additional development work be performed before the cermet anodes are used in commercial reduction cells. The results also highlight specific fabrication and operational considerations that should be addressed in future testing.

  4. Nanocomposite anode materials for sodium-ion batteries

    Science.gov (United States)

    Manthiram, Arumugam; Kim Il, Tae; Allcorn, Eric

    2016-06-14

    The disclosure relates to an anode material for a sodium-ion battery having the general formula AO.sub.x--C or AC.sub.x--C, where A is aluminum (Al), magnesium (Mg), titanium (Ti), vanadium (V), chromium (Cr), manganese (Mn), iron (Fe), cobalt (Co), nickel (Ni), zirconium (Zr), molybdenum (Mo), tungsten (W), niobium (Nb), tantalum (Ta), silicon (Si), or any combinations thereof. The anode material also contains an electrochemically active nanoparticles within the matrix. The nanoparticle may react with sodium ion (Na.sup.+) when placed in the anode of a sodium-ion battery. In more specific embodiments, the anode material may have the general formula M.sub.ySb-M'O.sub.x--C, Sb-MO.sub.x--C, M.sub.ySn-M'C.sub.x--C, or Sn-MC.sub.x--C. The disclosure also relates to rechargeable sodium-ion batteries containing these materials and methods of making these materials.

  5. ANODE CATALYST MATERIALS FOR USE IN FUEL CELLS

    DEFF Research Database (Denmark)

    2002-01-01

    a substrate material selected from Ru and Os; the respective components being present within specific ranges, display improved properties for use inanodes for low-temperature fuel cell anodes for PENFC fuel cells and direct methanol fuel cells....

  6. Na-Ion Battery Anodes: Materials and Electrochemistry.

    Science.gov (United States)

    Luo, Wei; Shen, Fei; Bommier, Clement; Zhu, Hongli; Ji, Xiulei; Hu, Liangbing

    2016-02-16

    The intermittent nature of renewable energy sources, such as solar and wind, calls for sustainable electrical energy storage (EES) technologies for stationary applications. Li will be simply too rare for Li-ion batteries (LIBs) to be used for large-scale storage purposes. In contrast, Na-ion batteries (NIBs) are highly promising to meet the demand of grid-level storage because Na is truly earth abundant and ubiquitous around the globe. Furthermore, NIBs share a similar rocking-chair operation mechanism with LIBs, which potentially provides high reversibility and long cycling life. It would be most efficient to transfer knowledge learned on LIBs during the last three decades to the development of NIBs. Following this logic, rapid progress has been made in NIB cathode materials, where layered metal oxides and polyanionic compounds exhibit encouraging results. On the anode side, pure graphite as the standard anode for LIBs can only form NaC64 in NIBs if solvent co-intercalation does not occur due to the unfavorable thermodynamics. In fact, it was the utilization of a carbon anode in LIBs that enabled the commercial successes. Anodes of metal-ion batteries determine key characteristics, such as safety and cycling life; thus, it is indispensable to identify suitable anode materials for NIBs. In this Account, we review recent development on anode materials for NIBs. Due to the limited space, we will mainly discuss carbon-based and alloy-based anodes and highlight progress made in our groups in this field. We first present what is known about the failure mechanism of graphite anode in NIBs. We then go on to discuss studies on hard carbon anodes, alloy-type anodes, and organic anodes. Especially, the multiple functions of natural cellulose that is used as a low-cost carbon precursor for mass production and as a soft substrate for tin anodes are highlighted. The strategies of minimizing the surface area of carbon anodes for improving the first-cycle Coulombic efficiency are

  7. Na-Ion Battery Anodes: Materials and Electrochemistry.

    Science.gov (United States)

    Luo, Wei; Shen, Fei; Bommier, Clement; Zhu, Hongli; Ji, Xiulei; Hu, Liangbing

    2016-02-16

    The intermittent nature of renewable energy sources, such as solar and wind, calls for sustainable electrical energy storage (EES) technologies for stationary applications. Li will be simply too rare for Li-ion batteries (LIBs) to be used for large-scale storage purposes. In contrast, Na-ion batteries (NIBs) are highly promising to meet the demand of grid-level storage because Na is truly earth abundant and ubiquitous around the globe. Furthermore, NIBs share a similar rocking-chair operation mechanism with LIBs, which potentially provides high reversibility and long cycling life. It would be most efficient to transfer knowledge learned on LIBs during the last three decades to the development of NIBs. Following this logic, rapid progress has been made in NIB cathode materials, where layered metal oxides and polyanionic compounds exhibit encouraging results. On the anode side, pure graphite as the standard anode for LIBs can only form NaC64 in NIBs if solvent co-intercalation does not occur due to the unfavorable thermodynamics. In fact, it was the utilization of a carbon anode in LIBs that enabled the commercial successes. Anodes of metal-ion batteries determine key characteristics, such as safety and cycling life; thus, it is indispensable to identify suitable anode materials for NIBs. In this Account, we review recent development on anode materials for NIBs. Due to the limited space, we will mainly discuss carbon-based and alloy-based anodes and highlight progress made in our groups in this field. We first present what is known about the failure mechanism of graphite anode in NIBs. We then go on to discuss studies on hard carbon anodes, alloy-type anodes, and organic anodes. Especially, the multiple functions of natural cellulose that is used as a low-cost carbon precursor for mass production and as a soft substrate for tin anodes are highlighted. The strategies of minimizing the surface area of carbon anodes for improving the first-cycle Coulombic efficiency are

  8. Carbon Fiber as Anode Material for Cathodic Prevention in Cementitious Materials

    OpenAIRE

    Zhang, Emma Qingnan; Tang, Luping; Zack, Thomas

    2016-01-01

    Cathodic prevention (CPre) technique is a promising method and has been used for the past two decades to prevent steel from corrosion in concrete structures. However, wide application of this technique has been restricted due to high costs of anode materials. In order to lower the cost and further improve this technique, carbon fiber composite anode has been introduced as an alternative anode material with affordable price and other outstanding properties. This paper presents the study of usi...

  9. Carbon Cryogel Silicon Composite Anode Materials for Lithium Ion Batteries

    Science.gov (United States)

    Woodworth James; Baldwin, Richard; Bennett, William

    2010-01-01

    A variety of materials are under investigation for use as anode materials in lithium-ion batteries, of which, the most promising are those containing silicon. 10 One such material is a composite formed via the dispersion of silicon in a resorcinol-formaldehyde (RF) gel followed by pyrolysis. Two silicon-carbon composite materials, carbon microspheres and nanofoams produced from nano-phase silicon impregnated RF gel precursors have been synthesized and investigated. Carbon microspheres are produced by forming the silicon-containing RF gel into microspheres whereas carbon nano-foams are produced by impregnating carbon fiber paper with the silicon containing RF gel to create a free standing electrode. 1-4,9 Both materials have demonstrated their ability to function as anodes and utilize the silicon present in the material. Stable reversible capacities above 400 mAh/g for the bulk material and above 1000 mAh/g of Si have been observed.

  10. Nanocomposite anode materials for sodium-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Manthiram, Arumugam; Kim Il, Tae; Allcorn, Eric

    2016-06-14

    The disclosure relates to an anode material for a sodium-ion battery having the general formula AO.sub.x--C or AC.sub.x--C, where A is aluminum (Al), magnesium (Mg), titanium (Ti), vanadium (V), chromium (Cr), manganese (Mn), iron (Fe), cobalt (Co), nickel (Ni), zirconium (Zr), molybdenum (Mo), tungsten (W), niobium (Nb), tantalum (Ta), silicon (Si), or any combinations thereof. The anode material also contains an electrochemically active nanoparticles within the matrix. The nanoparticle may react with sodium ion (Na.sup.+) when placed in the anode of a sodium-ion battery. In more specific embodiments, the anode material may have the general formula M.sub.ySb-M'O.sub.x--C, Sb-MO.sub.x--C, M.sub.ySn-M'C.sub.x--C, or Sn-MC.sub.x--C. The disclosure also relates to rechargeable sodium-ion batteries containing these materials and methods of making these materials.

  11. Optimization and Domestic Sourcing of Lithium Ion Battery Anode Materials

    Energy Technology Data Exchange (ETDEWEB)

    Wood, III, D. L.; Yoon, S. [A123 Systems, Inc.

    2012-10-25

    The purpose of this Cooperative Research and Development Agreement (CRADA) between ORNL and A123Systems, Inc. was to develop a low-temperature heat treatment process for natural graphite based anode materials for high-capacity and long-cycle-life lithium ion batteries. Three major problems currently plague state-of-the-art lithium ion battery anode materials. The first is the cost of the artificial graphite, which is heat-treated well in excess of 2000°C. Because of this high-temperature heat treatment, the anode active material significantly contributes to the cost of a lithium ion battery. The second problem is the limited specific capacity of state-of-the-art anodes based on artificial graphites, which is only about 200-350 mAh/g. This value needs to be increased to achieve high energy density when used with the low cell-voltage nanoparticle LiFePO4 cathode. Thirdly, the rate capability under cycling conditions of natural graphite based materials must be improved to match that of the nanoparticle LiFePO4. Natural graphite materials contain inherent crystallinity and lithium intercalation activity. They hold particular appeal, as they offer huge potential for industrial energy savings with the energy costs essentially subsidized by geological processes. Natural graphites have been heat-treated to a substantially lower temperature (as low as 1000-1500°C) and used as anode active materials to address the problems described above. Finally, corresponding graphitization and post-treatment processes were developed that are amenable to scaling to automotive quantities.

  12. Trends in Catalytic Activity for SOFC Anode materials

    DEFF Research Database (Denmark)

    Rossmeisl, Jan; Bessler, W. G.

    2008-01-01

    Quantum mechanical calculations on the level of density-functional theory are used to calculate the stability of surface-adsorbed hydrogen atoms, oxygen atoms, and hydroxyl radicals for a variety of metals (Mn, Fe, Co, Ni, Cu, Ru, Rh, Pd, Ag, Pt, Au) that may be used as electrode materials...... for solid oxide fuel cell (SOFC) anodes. The reaction energies along the hydrogen oxidation pathway were quantified for both, oxygen spillover and hydrogen spillover mechanisms at the three-phase boundary. The ab initio results are compared to previously-obtained experimental anode activities measured...... that oxygen spillover, where adsorbed oxygen is a key intermediate, is the dominant reaction pathway under the conditions used in the experiments. In this way the activity is linked directly to the microscopic binding affinities of reaction intermediates, providing a new understanding of the anode reaction...

  13. 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.

  14. Preparation and properties of antimony thin film anode materials

    Institute of Scientific and Technical Information of China (English)

    SU Shufa; CAO Gaoshao; ZHAO Xinbing

    2004-01-01

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

  15. Graphene composites as anode materials in lithium-ion batteries

    Science.gov (United States)

    Mazar Atabaki, M.; Kovacevic, R.

    2013-03-01

    Since the world of mobile phones and laptops has significantly altered by a big designer named Steve Jobs, the electronic industries have strived to prepare smaller, thinner and lower weight products. The giant electronic companies, therefore, compete in developing more efficient hardware such as batteries used inside the small metallic or polymeric frame. One of the most important materials in the production lines is the lithium-based batteries which is so famous for its ability in recharging as many times as a user needs. However, this is not an indication of being long lasted, as many of the electronic devices are frequently being used for a long time. The performance, chemistry, safety and above all cost of the lithium ion batteries should be considered when the design of the compounds are at the top concern of the engineers. To increase the efficiency of the batteries a combination of graphene and nanoparticles is recently introduced and it has shown to have enormous technological effect in enhancing the durability of the batteries. However, due to very high electronic conductivity, these materials can be thought of as preparing the anode electrode in the lithiumion battery. In this paper, the various approaches to characterize different types of graphene/nanoparticles and the process of preparing the anode for the lithium-ion batteries as well as their electrical properties are discussed.

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

    Science.gov (United States)

    Danilovic, Nemanja

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

  17. Material and Energy Flows in the Production of Cathode and Anode Materials for Lithium Ion Batteries

    Energy Technology Data Exchange (ETDEWEB)

    Dunn, Jennifer B. [Argonne National Lab. (ANL), Argonne, IL (United States); James, Christine [Michigan State Univ., East Lansing, MI (United States); Gaines, Linda [Argonne National Lab. (ANL), Argonne, IL (United States); Gallagher, Kevin [Argonne National Lab. (ANL), Argonne, IL (United States); Dai, Qiang [Argonne National Lab. (ANL), Argonne, IL (United States); Kelly, Jarod C. [Argonne National Lab. (ANL), Argonne, IL (United States)

    2015-09-01

    The Greenhouse gases, Regulated Emissions and Energy use in Transportation (GREET) model has been expanded to include four new cathode materials that can be used in the analysis of battery-powered vehicles: lithium nickel cobalt manganese oxide (LiNi0.4Co0.2Mn0.4O2 [NMC]), lithium iron phosphate (LiFePO4 [LFP]), lithium cobalt oxide (LiCoO2 [LCO]), and an advanced lithium cathode (0.5Li2MnO3∙0.5LiNi0.44Co0.25Mn0.31O2 [LMR-NMC]). In GREET, these cathode materials are incorporated into batteries with graphite anodes. In the case of the LMR-NMC cathode, the anode is either graphite or a graphite-silicon blend. Lithium metal is also an emerging anode material. This report documents the material and energy flows of producing each of these cathode and anode materials from raw material extraction through the preparation stage. For some cathode materials, we considered solid state and hydrothermal preparation methods. Further, we used Argonne National Laboratory’s Battery Performance and Cost (BatPaC) model to determine battery composition (e.g., masses of cathode, anode, electrolyte, housing materials) when different cathode materials were used in the battery. Our analysis concluded that cobalt- and nickel-containing compounds are the most energy intensive to produce.

  18. Pulsed laser deposited Si on multilayer graphene as anode material for lithium ion batteries

    OpenAIRE

    Gouri Radhakrishnan; Paul M. Adams; Brendan Foran; Michael V. Quinzio; Miles J. Brodie

    2013-01-01

    Pulsed laser deposition and chemical vapor deposition were used to deposit very thin silicon on multilayer graphene (MLG) on a nickel foam substrate for application as an anode material for lithium ion batteries. The as-grown material was directly fabricated into an anode without a binder, and tested in a half-cell configuration. Even under stressful voltage limits that accelerate degradation, the Si-MLG films displayed higher stability than Si-only electrodes. Post-cycling images of the anod...

  19. Lithium-Ion-Battery Anode Materials with Improved Capacity from a Metal-Organic Framework.

    Science.gov (United States)

    Lin, Xiao-Ming; Niu, Ji-Liang; Lin, Jia; Wei, Lei-Ming; Hu, Lei; Zhang, Gang; Cai, Yue-Peng

    2016-09-01

    We present a porous metal-organic framework (MOF) with remarkable thermal stability that exhibits a discharge capacity of 300 mAh g(-1) as an anode material for a lithium-ion battery. Pyrolysis of the obtained MOF gives an anode material with improved capacity (741 mAh g(-1)) and superior cyclic stability. PMID:27548622

  20. Building Self-Healing Alloy Architecture for Stable Sodium-Ion Battery Anodes: A Case Study of Tin Anode Materials.

    Science.gov (United States)

    Mao, Jianfeng; Fan, Xiulin; Luo, Chao; Wang, Chunsheng

    2016-03-23

    The rational design of anode materials is a challenge in developing sodium ion batteries. Alloy anodes provide high gravimetric and volumetric capacities but suffer the short cycle life as a result of the continuous and accumulated pulverization, resulting from a large volume change during the cycling process. Herein, using pure Sn, an irreversible conversion reaction combined with an alloy reaction (SnO), and a reversible conversion reaction combined with an alloy reaction (Sn4P3) as samples, we demonstrate that the pulverization and aggregation of the alloy anode can be partially recovered and the accumulation of pulverization and aggregation during charge/discharge cycles can be terminated using a reversible conversion reaction combined with an alloy reaction. The cycling stability of three Sn-based anodes increases in order of Sn4P3 > SnO > Sn. The enhancement in Sn4P3 can be attributed to a reversible reaction of Sn4P3 + 9Na ↔ 4Sn + 3Na3P, which repairs the cracks, damage, and aggregation of Sn particles that occurred in the alloy process of 4Sn + 15Na ↔ Na15Sn4 during cycling and, hence, terminates the pulverization. The repair mechanism looks like the self-healing feature in nature, where the damage can be healed by itself. Therefore, the suggested mechanism can be called self-healing, while the repaired anode can be termed as the self-healing anode. The use of self-healing strategies to build an electrode architecture is new and highly desirable because it can increase the cycle life and provide a general approach toward stable electrode materials. PMID:26937998

  1. Metal carbonates as anode materials for lithium ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Shao, Lianyi; Ma, Rui; Wu, Kaiqiang; Shui, Miao; Lao, Mengmeng; Wang, Dongjie; Long, Nengbing; Ren, Yuanlong; Shu, Jie, E-mail: sergio_shu@hotmail.com

    2013-12-25

    Highlights: •Metal carbonates are probable anode materials for lithium ion batteries. •CoCO{sub 3}/C composite can deliver an initial discharge capacity of 2096.6 mAh g{sup −1} . •Co, Li{sub 2}CO{sub 3}, Li{sub 2}O, and low-valence carbon are final lithiated products for CoCO{sub 3}. -- Abstract: Six metal carbonates (Li{sub 2}CO{sub 3}, Na{sub 2}CO{sub 3}, SrCO{sub 3}, BaCO{sub 3}, K{sub 2}CO{sub 3}, CoCO{sub 3}) are tested and compared as anode materials for lithium ion batteries. The electrochemical results show that only CoCO{sub 3} is electrochemically active material and can deliver a high initial capacity of 1425.9 mAh g{sup −1}. The lithium storage mechanism in CoCO{sub 3} is studied by ex situ X-ray diffraction technique, ex situ infrared method, ex situ X-ray photoelectron spectroscopy and in situ X-ray diffraction technique. It is found that the electrochemical reactions between CoCO{sub 3} and Li firstly result in the formation of metal Co and Li{sub 2}CO{sub 3}, and then partial Li{sub 2}CO{sub 3} is further reduced into carbon (C{sup 0}), low-valence carbon (C{sup 2+}), and Li{sub 2}O. It also demonstrates that the electrochemical reaction between CoCO{sub 3} and Li is a partially reversible process. Based on these electrochemical results, it is obvious that narrow potential range can acquire a better reversibility for CoCO{sub 3}/Li batteries by suppressing particle pulverization. Besides, the comparison of CoCO{sub 3}, ball-milled CoCO{sub 3} and ball-milled CoCO{sub 3}/C composite also indicates that smaller active particle and carbon buffer are beneficial to obtain better cycling performance and higher reversible capacity.

  2. Pulsed laser deposited Si on multilayer graphene as anode material for lithium ion batteries

    Directory of Open Access Journals (Sweden)

    Gouri Radhakrishnan

    2013-12-01

    Full Text Available Pulsed laser deposition and chemical vapor deposition were used to deposit very thin silicon on multilayer graphene (MLG on a nickel foam substrate for application as an anode material for lithium ion batteries. The as-grown material was directly fabricated into an anode without a binder, and tested in a half-cell configuration. Even under stressful voltage limits that accelerate degradation, the Si-MLG films displayed higher stability than Si-only electrodes. Post-cycling images of the anodes reveal the differences between the two material systems and emphasize the role of the graphene layers in improving adhesion and electrochemical stability of the Si.

  3. Tremella-like Molybdenum Dioxide as an Anode Material for Lithium ion Battery

    Institute of Scientific and Technical Information of China (English)

    L.C.Yang; Q.S.Gao; Y.H.Zhang; Y.Tang; Y.P.Wu

    2007-01-01

    1 Results Molybdenum dioxide, with excellent chemical and physical properties, has been widely used in various fields[1]. As an anode material for lithium ion battery, it exhibits higher capacity than commercial carbonaceous materials, and proper morphology, structure and particle size are necessary for MoO2 to be employed as an anode material for lithium ion battery[2].We have successfully obtained tremella-like structure self-assembled with hexagonal MoO2 nanosheets via hydrothermal method using ethyl...

  4. Cyclic performance of silicon as anode material in lithium ion batteries

    OpenAIRE

    Kim, Seongseop; Cho, Maenghyo; Zhou, Min

    2014-01-01

    Silicon is a promising anode material owing to its high energy density which is an important aspect of the -performance metric for lithium ion batteries. In this study, the cyclic behavior of silicon as the anode material in lithium ion batteries is investigated. Chemical–mechanical coupling is considered to analyze the interactions between diffusion and factors influencing the mechanical response of materials. Galvanostatic–potentiostatic -charging/discharging cycles are used to investigate ...

  5. Porous Silicon as Anode Material for Li-ion Batteries : Structure and Performance

    OpenAIRE

    Ulvestad, Asbjørn

    2013-01-01

    Silicon has proven to have a great potential as anode material in lithium-ion batteries due to its high theoretical electrochemical capacity. However, silicon anodes deteriorate quickly during cyclic charging and discharging, rendering them useless in only a few cycles. This has been attributed to the stresses induced by the large volume change of the material during cycling. By using finely structured silicon, these stresses can be effectively reduced, in what is aptly called dimensional sta...

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

    Science.gov (United States)

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

    2016-05-01

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

  7. An investigation of anode and cathode materials in photomicrobial fuel cells.

    Science.gov (United States)

    Schneider, Kenneth; Thorne, Rebecca J; Cameron, Petra J

    2016-02-28

    Photomicrobial fuel cells (p-MFCs) are devices that use photosynthetic organisms (such as cyanobacteria or algae) to turn light energy into electrical energy. In a p-MFC, the anode accepts electrons from microorganisms that are either growing directly on the anode surface (biofilm) or are free floating in solution (planktonic). The nature of both the anode and cathode material is critical for device efficiency. An ideal anode is biocompatible and facilitates direct electron transfer from the microorganisms, with no need for an electron mediator. For a p-MFC, there is the additional requirement that the anode should not prevent light from perfusing through the photosynthetic cells. The cathode should facilitate the rapid reaction of protons and oxygen to form water so as not to rate limit the device. In this paper, we first review the range of anode and cathode materials currently used in p-MFCs. We then present our own data comparing cathode materials in a p-MFC and our first results using porous ceramic anodes in a mediator-free p-MFC.

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2011-01-10

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

  9. Selection of Anodic Material Used in Electrolytic Process for Producing Hypophosphorous Acid

    Institute of Scientific and Technical Information of China (English)

    Fu Sheng WANG; Bing Kui SONG; Xiao Li HAN; Bao Gui ZHANG

    2004-01-01

    Black lead, Ti-Ru and Ti-PbO2 were used as anode and stainless steel was used as cathode.The electrolytic process of producing hypophosphorous acid with four-compartment electrodialytic cell was studied. The comparison of some factors, such as anodic voltage, product concentration and current efficiency, of black lead, Ti-Ru, and Ti-PbO2 electrodes was conducted. As a result, the Ti-PbO2 electrode is the optimal anode material used, it can be in electrolytic process for producing hypophosphorous acid.

  10. Novel Ceramic Materials for Polymer Electrolyte Membrane Water Electrolysers' Anodes

    DEFF Research Database (Denmark)

    Polonsky, J.; Bouzek, K.; Prag, Carsten Brorson;

    2012-01-01

    Tantalum carbide was evaluated as a possible new support for the IrO2 for use in anodes of polymer electrolyte membrane water electrolysers. A series of supported electrocatalysts varying in mass content of iridium oxide was prepared. XRD, powder conductivity measurements and cyclic and linear...... sweep voltammetry were used to characterise the electrocatalysts. The most performing composition was found to lie between 50 and 90 wt.% IrO2 on TaC...

  11. Investigation of Anode Materials for Lithium Ion Batteries

    OpenAIRE

    Zhong, Lanlan

    2016-01-01

    Lithium ion batteries, Lithium ion batteries (LIBs) have for several years dominated the market for cell phones, laptops, and several other portable electronic devices. In order to match the necessity of increasing need for higher energy density storage devices, for example, hybrid/electric vehicles. Higher energy density lithium ion batteries have to be investigated. Anode as one of the most important components of in LIBs has been intensively studied in recent years. Silicon, tin and metal...

  12. A disordered carbon as a novel anode material in lithium-ion cells

    Energy Technology Data Exchange (ETDEWEB)

    Bonino, F.; Brutti, S.; Reale, P.; Scrosati, B. [Dipartimento di Chimica, Universita ' ' La Sapienza' ' , I-00185 Rome (Italy); Gherghel, L.; Wu, J.; Muellen, K. [Max Planck Institute for Polymer Research, Ackermannweg 10, D-55124 Mainz (Germany)

    2005-03-22

    The electrochemical behavior of a disordered carbon used as the anode in a lithium battery has been tested. The characteristics of this carbon, especially its specific capacity and cycle life, are such that it is a potentially unique, high-performance anode material for new types of lithium-ion batteries. The Figure shows the specific capacity versus cycle number of the disordered carbon electrode in a lithium-ion cell. (Abstract Copyright [2005], Wiley Periodicals, Inc.)

  13. Alternative anode materials for solid oxide fuel cells

    Energy Technology Data Exchange (ETDEWEB)

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

    2007-11-08

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

  14. Nanotemplated platinum fuel cell catalysts and copper-tin lithium battery anode materials for microenergy devices

    Energy Technology Data Exchange (ETDEWEB)

    Rohan, J.F., E-mail: james.rohan@tyndall.ie [Tyndall National Institute, University College Cork, Lee Maltings, Cork (Ireland); Hasan, M.; Holubowitch, N. [Tyndall National Institute, University College Cork, Lee Maltings, Cork (Ireland)

    2011-11-01

    Highlights: > Anodic Aluminum oxide formation on Si substrate. > High density nanotemplated Pt catalyst on Si for integrated energy and electronics. > CuSn alloy deposition from a single, high efficiency methanesulfonate plating bath. > Nanotemplated CuSn Li anode electrodes with high capacity retention. - Abstract: Nanotemplated materials have significant potential for applications in energy conversion and storage devices due to their unique physical properties. Nanostructured materials provide additional electrode surface area beneficial for energy conversion or storage applications with short path lengths for electronic and ionic transport and thus the possibility of higher reaction rates. We report on the use of controlled growth of metal and alloy electrodeposited templated nanostructures for energy applications. Anodic aluminium oxide templates fabricated on Si for energy materials integration with electronic devices and their use for fuel cell and battery materials deposition is discussed. Nanostructured Pt anode catalysts for methanol fuel cells are shown. Templated CuSn alloy anodes that possess high capacity retention with cycling for lithium microbattery integration are also presented.

  15. Dissolution of Plutonium Scrub Alloy and Anode Heel Materials in H-Canyon

    International Nuclear Information System (INIS)

    H-Canyon has a ''gap'' in dissolver operations during the last three months of FY03. One group of material to be processed during the gap is pre-existing scrub alloy material. There are 14 cans of material containing approximately 3.8 kilograms of plutonium. Of the 14 cans, it was anticipated that four cans contain salts, two cans contain anode heel materials, and eight cans contain scrub alloy buttons. H-Canyon desires to process the materials using a flowsheet similar to the SS and C (sand, slag and crucible) dissolution flowsheet used in F-Canyon. The materials will be loaded into carbon steel cans and then placed into aluminum metal charging bundles. Samples were sent to Savannah River Technology Center (SRTC) for characterization and flowsheet testing -- four MSE salts, two anode heels, and seven scrub alloy buttons. SRTC dissolved and characterized each of the samples. Two of them, originally thought to be MSE salts, were found to be graphite mold materials and were unsuitable for processing in H-Canyon. Characterization studies confirmed that the identification of the remaining items as MSE salts, scrub alloy buttons, and anode heel materials was correct. The MSE salts and anode heels solids are comprised primarily of plutonium, potassium, sodium and chloride. Both the MSE salts and anode heels left behind small amounts of residual solids. The scrub alloy buttons are comprised primarily of plutonium and aluminum. The solids dissolve readily with light, effervescent gas generation at the material surface and only trace amounts of NOx generation. Of the seven button samples, four dissolved completely. Two button samples contained small amounts of tantalum that did not dissolve. The last of the seven scrub alloy samples left a trace amount of residual plutonium solids. It is anticipated that the presence of undissolved fissile material is a function of where the sample was located relative to the button surface

  16. Nano-sized carboxylates as anode materials for rechargeable lithium-ion batteries

    Institute of Scientific and Technical Information of China (English)

    Xiaoyan Wu; Jie Ma; Yong-Sheng Hu; Hong Li; Liquan Chen

    2014-01-01

    Nano-sized carboxylates Na2C7H3NO4 and Na2C6H2N2O4 were prepared and investigated as anode materials for lithium-ion batteries. Both carboxylates exhibit high reversible capacities around 190 mAh/g above a cut-off voltage of 0.8 V vs. Li+/Li, potentially improving the safety of the batteries. In addition, good rate performance and long cycle life of these carboxylates make them promising candidates as anode materials for lithium-ion batteries.

  17. Hybrid Direct Carbon Fuel Cell Performance with Anode Current Collector Material

    DEFF Research Database (Denmark)

    Deleebeeck, Lisa; Kammer Hansen, Kent

    2015-01-01

    The influence of the current collector on the performance of a hybrid direct carbon fuel cell (HDCFC), consisting of solid oxide fuel cell (SOFC) with a molten carbonate-carbon slurry in contact with the anode, has been investigated using current-voltage curves. Four different anode current...... collectors were studied: Au, Ni, Ag, and Pt. It was shown that the performance of the direct carbon fuel cell (DCFC) is dependent on the current collector materials, Ni and Pt giving the best performance, due to their catalytic activity. Gold is suggested to be the best material as an inert current collector...

  18. Carbon Cryogel and Carbon Paper-Based Silicon Composite Anode Materials for Lithium-Ion Batteries

    Science.gov (United States)

    Woodworth, James; Baldwin, Richard; Bennett, William

    2010-01-01

    A variety of materials are under investigation for use as anode materials in lithium-ion batteries, of which, the most promising are those containing silicon. 6 One such material is a composite formed via the dispersion of silicon in a resorcinol-formaldehyde (RF) gel followed by pyrolysis. Two silicon-carbon composite materials, carbon microspheres and nanofoams produced from nano-phase silicon impregnated RF gel precursors have been synthesized and investigated. Carbon microspheres are produced by forming the silicon-containing RF gel into microspheres whereas carbon nano-foams are produced by impregnating carbon fiber paper with the silicon containing RF gel to create a free standing electrode. 1-5 Both materials have demonstrated their ability to function as anodes and utilize the silicon present in the material. Stable reversible capacities above 400 mAh/g for the bulk material and above 1000 mAh/g of Si have been observed.

  19. Silicon Composite Anode Materials for Lithium Ion Batteries Based on Carbon Cryogels and Carbon Paper

    Science.gov (United States)

    Woodworth, James; Baldwin, Richard; Bennett, William

    2010-01-01

    A variety of materials are under investigation for use as anode materials in lithium-ion batteries, of which, the most promising are those containing silicon. One such material is a composite formed via the dispersion of silicon in a resorcinol-formaldehyde (RF) gel followed by pyrolysis. Two silicon-carbon composite materials, carbon microspheres and nanofoams produced from nano-phase silicon impregnated RF gel precursors have been synthesized and investigated. Carbon microspheres are produced by forming the silicon-containing RF gel into microspheres whereas carbon nanofoams are produced by impregnating carbon fiber paper with the silicon containing RF gel to create a free standing electrode. Both materials have demonstrated their ability to function as anodes and utilize the silicon present in the material. Stable reversible capacities above 400 mAh/g for the bulk material and above 1000 mAh/g of Si have been observed.

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

    International Nuclear Information System (INIS)

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

  1. Synthesis, Characterization and Testing of Novel Anode and Cathode Materials for Li-Ion Batteries

    Energy Technology Data Exchange (ETDEWEB)

    White, Ralph E.; Popov, Branko N.

    2002-10-31

    During this program we have synthesized and characterized several novel cathode and anode materials for application in Li-ion batteries. Novel synthesis routes like chemical doping, electroless deposition and sol-gel method have been used and techniques like impedance, cyclic voltammetry and charge-discharge cycling have been used to characterize these materials. Mathematical models have also been developed to fit the experimental result, thus helping in understanding the mechanisms of these materials.

  2. Study of Silicon Oxycarbide(SiOC) as Anode Materials for Li-ion Batteries

    OpenAIRE

    Vallachira Warriam Sasikumar Pradeep, Pradeep

    2013-01-01

    The principal object of this thesis is the investigation of silicon oxycarbide (SiOC) ceramics as anode material for Li-ion batteries. The investigated materials are prepared by cross linking commercial polymer siloxanes via hydrosylilation reactions or hybrid alkoxide precursors via sol-gel. The cross linked polymer networks are then converted in to ceramic materials by a pyrolysis process in controlled argon atmosphere at 800-1300 °C. In details the influence of carbon content on lithium...

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

    Science.gov (United States)

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

    2014-04-23

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

  4. Electrochemical Characteristics of Tin Oxide-Graphite as Anode Material for Lithium-ion Cells

    Science.gov (United States)

    Hasanaly, Siti Munirah

    2010-03-01

    Tin oxide anode materials used in lithium-ion cells experience large volume changes during charging and discharging which cause substantial losses in capacity. In this work, the tin oxide-graphite composite is proposed as an alternative anode material to overcome this problem. The composite was synthesised from a solution of tin chloride dihydrate and graphite powders with citric acid as the chelating agent. In this sol-gel method, a solid phase is formed through a chemical reaction in a liquid phase at moderate temperature. The technique offers several advantages compared to the solid state synthesis technique such as the ability to maintain the homogeneous mixture of precursors during synthesis and to produce small particles. The electrochemical behaviour of the anode material was investigated by means of galvanostatic charge discharge technique. An initial reversible capacity of 748 mAh/g is obtained and nearly 600 mAh/g was retained upon the reaching the fifth cycle. This study shows that the presence of graphite is able to minimise the agglomeration of tin particles that causes large volume changes during cycling, thereby improving cyclability of the anode material.

  5. Submicron organic nanofiber devices with different anode-cathode materials: A simple approach

    DEFF Research Database (Denmark)

    Henrichsen, Henrik Hartmann; Sturm, Heinz; Bøggild, Peter;

    2010-01-01

    The authors present a simple general method for simultaneously producing tens of submicron electrode gaps with different cathode and anode materials on top of nanofibers, nanowires, and nanotubes, with an optional gap size variation. Using this method, an ensemble of para-hexaphenylene (p6P...

  6. Carbon-Coated SnO2 Nanorod Array for Lithium-Ion Battery Anode Material

    Directory of Open Access Journals (Sweden)

    Ji Xiaoxu

    2010-01-01

    Full Text Available Abstract Carbon-coated SnO2 nanorod array directly grown on the substrate has been prepared by a two-step hydrothermal method for anode material of lithium-ion batteries (LIBs. The structural, morphological and electrochemical properties were investigated by means of X-ray diffraction (XRD, scanning electron microscopy (SEM, transmission electron microscopy (TEM and electrochemical measurement. When used as anodes for LIBs with high current density, as-obtained array reveals excellent cycling stability and rate capability. This straightforward approach can be extended to the synthesis of other carbon-coated metal oxides for application of LIBs.

  7. Tantalum carbide as a novel support material for anode electrocatalysts in polymer electrolyte membrane water electrolysers

    OpenAIRE

    Polonský, Jakub; Petrushina, Irina; Christensen, Erik; Bouzek, K.; Prag, Carsten Brorson; Andersen, Jens Enevold Thaulov; Bjerrum, Niels

    2012-01-01

    Iridium oxide (IrO2) currently represents a state of the art electrocatalyst for anodic oxygen evolution. Since iridium is both expensive and scarce, the future practical application of this process makes it essential to reduce IrO2 loading on the anodes of PEM water electrolysers. In the present study an approach to utilising a suitable electrocatalyst support was followed. Of the materials selected from a literature review, TaC has proved to be stable under the conditions of the accelerated...

  8. Evaluation of anode (electro)catalytic materials for the direct borohydride fuel cell: Methods and benchmarks

    Science.gov (United States)

    Olu, Pierre-Yves; Job, Nathalie; Chatenet, Marian

    2016-09-01

    In this paper, different methods are discussed for the evaluation of the potential of a given catalyst, in view of an application as a direct borohydride fuel cell DBFC anode material. Characterizations results in DBFC configuration are notably analyzed at the light of important experimental variables which influence the performances of the DBFC. However, in many practical DBFC-oriented studies, these various experimental variables prevent one to isolate the influence of the anode catalyst on the cell performances. Thus, the electrochemical three-electrode cell is a widely-employed and useful tool to isolate the DBFC anode catalyst and to investigate its electrocatalytic activity towards the borohydride oxidation reaction (BOR) in the absence of other limitations. This article reviews selected results for different types of catalysts in electrochemical cell containing a sodium borohydride alkaline electrolyte. In particular, propositions of common experimental conditions and benchmarks are given for practical evaluation of the electrocatalytic activity towards the BOR in three-electrode cell configuration. The major issue of gaseous hydrogen generation and escape upon DBFC operation is also addressed through a comprehensive review of various results depending on the anode composition. At last, preliminary concerns are raised about the stability of potential anode catalysts upon DBFC operation.

  9. Nanoscale Engineering of Heterostructured Anode Materials for Boosting Lithium-Ion Storage.

    Science.gov (United States)

    Chen, Gen; Yan, Litao; Luo, Hongmei; Guo, Shaojun

    2016-09-01

    Rechargeable lithium-ion batteries (LIBs), as one of the most important electrochemical energy-storage devices, currently provide the dominant power source for a range of devices, including portable electronic devices and electric vehicles, due to their high energy and power densities. The interest in exploring new electrode materials for LIBs has been drastically increasing due to the surging demands for clean energy. However, the challenging issues essential to the development of electrode materials are their low lithium capacity, poor rate ability, and low cycling stability, which strongly limit their practical applications. Recent remarkable advances in material science and nanotechnology enable rational design of heterostructured nanomaterials with optimized composition and fine nanostructure, providing new opportunities for enhancing electrochemical performance. Here, the progress as to how to design new types of heterostructured anode materials for enhancing LIBs is reviewed, in the terms of capacity, rate ability, and cycling stability: i) carbon-nanomaterials-supported heterostructured anode materials; ii) conducting-polymer-coated electrode materials; iii) inorganic transition-metal compounds with core@shell structures; and iv) combined strategies to novel heterostructures. By applying different strategies, nanoscale heterostructured anode materials with reduced size, large surfaces area, enhanced electronic conductivity, structural stability, and fast electron and ion transport, are explored for boosting LIBs in terms of high capacity, long cycling lifespan, and high rate durability. Finally, the challenges and perspectives of future materials design for high-performance LIB anodes are considered. The strategies discussed here not only provide promising electrode materials for energy storage, but also offer opportunities in being extended for making a variety of novel heterostructured nanomaterials for practical renewable energy applications.

  10. SiCN based Anode Materials for Lithium-Ion Batteries

    OpenAIRE

    Reinold, Lukas Mirko

    2016-01-01

    This thesis deals with the investigation of polymer-derived silicon carbonitride based anode materials for their application in lithium-ion batteries. Carbon-rich silicon carbonitrides are obtained by a pyrolysis of different organosilicon precursors, namely poly(phenylvinylsilylcarbodiimide), poly(phenylvinylsilazane), poly(diphenylsilylcarbodiimide), poly(phenylsilsesquicarbodiimide) and poly(phenylsilsesquiazane). The materials are characterized by means of Raman spectroscopy, elemental an...

  11. Review on recent progress of nanostructured anode materials for Li-ion batteries

    KAUST Repository

    Goriparti, Subrahmanyam

    2014-07-01

    This review highlights the recent research advances in active nanostructured anode materials for the next generation of Li-ion batteries (LIBs). In fact, in order to address both energy and power demands of secondary LIBs for future energy storage applications, it is required the development of innovative kinds of electrodes. Nanostructured materials based on carbon, metal/semiconductor, metal oxides and metal phosphides/nitrides/sulfides show a variety of admirable properties for LIBs applications such as high surface area, low diffusion distance, high electrical and ionic conductivity. Therefore, nanosized active materials are extremely promising for bridging the gap towards the realization of the next generation of LIBs with high reversible capacities, increased power capability, long cycling stability and free from safety concerns. In this review, anode materials are classified, depending on their electrochemical reaction with lithium, into three groups: intercalation/de-intercalation, alloy/de-alloy and conversion materials. Furthermore, the effect of nanoscale size and morphology on the electrochemical performance is presented. Synthesis of the nanostructures, lithium battery performance and electrode reaction mechanisms are also discussed. To conclude, the main aim of this review is to provide an organic outline of the wide range of recent research progresses and perspectives on nanosized active anode materials for future LIBs.

  12. Investigation of residual anode material after electrorefining uranium in molten chloride salt

    Science.gov (United States)

    Rose, M. A.; Williamson, M. A.; Willit, J.

    2015-12-01

    A buildup of material at uranium anodes during uranium electrorefining in molten chloride salts has been observed. Potentiodynamic testing has been conducted using a three electrode cell, with a uranium working electrode in both LiCl/KCl eutectic and LiCl each containing ∼5 mol% UCl3. The anodic current response was observed at 50° intervals between 450 °C and 650 °C in the eutectic salt. These tests revealed a buildup of material at the anode in LiCl/KCl salt, which was sampled at room temperature, and analyzed using ICP-MS, XRD and SEM techniques. Examination of the analytical data, current response curves and published phase diagrams has established that as the uranium anode dissolves, the U3+ ion concentration in the diffusion layer surrounding the electrode rises precipitously to levels, which may at low temperatures exceed the solubility limit for UCl3 or in the case of the eutectic salt for K2UCl5. The reduction in current response observed at low temperature in eutectic salt is eliminated at 650 °C, where K2UCl5 is absent due to its congruent melting and only simple concentration polarization effects are seen. In LiCl similar concentration effects are seen though significantly longer time at applied potential is required to effect a reduction in the current response as compared to the eutectic salt.

  13. Porous silicon based anode material formed using metal reduction

    Energy Technology Data Exchange (ETDEWEB)

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

    2015-09-22

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

  14. Synthesis of nano Sb-encapsulated pyrolytic polyacrylonitrile composite for anode material in lithium secondary batteries

    Energy Technology Data Exchange (ETDEWEB)

    He, Xiangming; Pu, Weihua; Wang, Li; Ren, Jianguo; Jiang, Changyin; Wan, Chunrong [Institute of Nuclear and New Energy Technology, Tsinghua University, Beijing 100084 (China)

    2007-03-01

    A novel process was proposed to synthesize nano Sb-encapsulated pyrolytic polyacrylonitrile composite for anode material in lithium secondary batteries. The preparation started with the dissolution of SbCl{sub 3} and polyacrylonitrile (PAN) in dimethylformamide (DMF) solution, followed by the addition of KBH{sub 4} to reduce Sb{sup 3+} in the solution. The Sb composite was obtained by pyrolysis of the Sb/PAN mixture that precipitated out when the DMF solution was added by plentiful water. The TEM analysis showed that about 100-200 nm Sb particles were embedded by the pyrolyzed PAN, which provided a conductive matrix to relieve the morphological change of Sb during electrochemical cycling. As-prepared composite presented good cycleability for lithium storage. The proposed process paves an effective way to prepare high performance alloy based composite anode materials for high performance lithium-ion batteries. (author)

  15. Relationship between initial efficiency and structure parameters of carbon anode material for Li-ion battery

    Institute of Scientific and Technical Information of China (English)

    SHEN Jian-bin; TANG You-gen; LIANG Yi-zeng; TAN Xin-xin

    2008-01-01

    The initial efficiency is a very important criterion for carbon anode material of Li-ion battery. The relationship between initial efficiency and structure parameters of carbon anode material of Li-ion battery was investigated by an artificial intelligence approach called Random Forests using D10, D50, D90, BET specific surface area and TP density as inputs, initial efficiency as output.The results give good classification performance with 91% accuracy. The variable importance analysis results show the impact of 5 variables on the initial efficiency descends in the order of D90, TP density, BET specific surface area, D50 and D10; smaller D90 and larger TP density have positive impact on initial efficiency. The contribution of BET specific surface area on classification is only 18.74%, which indicates the shortcoming of BET specific surface area as a widely used parameter for initial efficiency evaluation.

  16. 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.

  17. Facile synthesis of one-dimensional zinc vanadate nanofibers for high lithium storage anode material

    International Nuclear Information System (INIS)

    One-dimensional (1D) zinc vanadate (α-Zn2V2O7) nanofibers have been synthesized through electrospinning combined with an annealing process. When used as anode material for lithium-ion batteries (LIBs), electrospun 1D α-Zn2V2O7 nanofibers exhibit a reversible capacity of ∼708 mAh g−1 after 100 cycles at a current density of 50 mA g−1. A good rate capability is also achieved even at higher current densities. When cycled at a current density of 2000 mA g−1, the electrode can still show a reversible capacity of ∼311 mAh g−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-Zn2V2O7 nanofibers, which are promising high-performance anode materials for LIBs. - Highlights: • Electrospun 1D α-Zn2V2O7 nanofibers are first synthesized for anode material. • The electrochemical reaction mechanism of this material is discussed. • A reversible capacity of ∼708 mAh g−1 is obtained after 100 cycles at 50 mA g−1. • 1D α-Zn2V2O7 nanofiber anodes show excellent rate capability for LIBs

  18. Enhancement of Electrochemical Stability about Silicon/Carbon Composite Anode Materials for Lithium Ion Batteries

    OpenAIRE

    Wei Xiao; Chang Miao; Xuemin Yan; Qing Sun; Ping Mei

    2015-01-01

    Silicon/carbon (Si/C) composite anode materials are successfully synthesized by mechanical ball milling followed by pyrolysis method. The structure and morphology of the composite are characterized by X-ray diffraction and scanning electron microscopy and transmission electron microscope, respectively. The results show that the composite is composed of Si, flake graphite, and phenolic resin-pyrolyzed carbon, and Si and flake graphite are enwrapped by phenolic resin-pyrolyzed carbon, which can...

  19. A Chemo-Mechanical model of delithiation in high-capacity anode materials

    OpenAIRE

    Yang, Hui; Zhang, Sulin

    2014-01-01

    We present a chemo-mechanical model to investigate the delithiation-induced phase transformation, morphological evolution, stress generation, void nucleation, and growth in high-capacity anode materials such as silicon (Si) and germanium (Ge). The model couples lithium (Li) diffusion with large elasto-plastic deformation by solving a set of coupled phase field and mechanical equilibrium equations using the finite element method, which leads to the coevolution of the Li concentration, stress d...

  20. Bismuth Nanoparticles Embedded in Carbon Spheres as Anode Materials for Sodium/Lithium-Ion Batteries.

    Science.gov (United States)

    Yang, Fuhua; Yu, Fan; Zhang, Zhian; Zhang, Kai; Lai, Yanqing; Li, Jie

    2016-02-12

    Sodium-ion batteries (SIBs) are regarded as an attractive alternative to lithium-ion batteries (LIBs) for large-scale commercial applications, because of the abundant terrestrial reserves of sodium. Exporting suitable anode materials is the key to the development of SIBs and LIBs. In this contribution, we report on the fabrication of Bi@C microspheres using aerosol spray pyrolysis technique. When used as SIBs anode materials, the Bi@C microsphere delivered a high capacity of 123.5 mAh g(-1) after 100 cycles at 100 mA g(-1) . The rate performance is also impressive (specific capacities of 299, 252, 192, 141, and 90 mAh g(-1) are obtained under current densities of 0.1, 0.2, 0.5, 1, and 2 A g(-1) , respectively). Furthermore, the Bi@C microsphere also proved to be suitable LIB anode materials. The excellent electrochemical performance for both SIBs and LIBs can attributed to the Bi@C microsphere structure with Bi nanoparticles uniformly dispersed in carbon spheres.

  1. Recovery of valuable metals from anode material of hydrogen-nickel battery

    Institute of Scientific and Technical Information of China (English)

    WU Fang; XU Sheng-ming; LI Lin-yan; CHEN Song-zhe; XU Gang; XU Jing-ming

    2009-01-01

    Simultaneous recovery of rare earth, nickel and cobalt resources from the anode material of hydrogen-nickel battery was performed through a hydrometallurgical process. Most of rare earth elements are separated from nickel and cobalt in the form of sulfates when the anode material is firstly leached with sulfuric acid. Then, the precipitated rare earth sulfates are dissolved with sodium hydroxide to form rare earth hydroxides. The rare earth element, zinc and manganese ions in the lixivium are also separated from nickel and cobalt by using PC-88A extractant system, and the organic phase loaded rare earth is stripped with hydrochloric acid. By neutralizing the stripping solution with rare earth hydroxide, the rare earth chloride is obtained. Under the suitable leaching conditions of sulfuric acid 3 mol/L, leaching time 4 h and temperature 95 ℃, 94.5% of rare earth in the anode material is transformed into the sulfate precipitates, and the leaching ratios of nickel and cobalt can approach 99.5%. When the pH value of the extractive system is controlled in the range of 3.0-3.5, the rare earth elements in the lixivium can be extracted completely into the organic phase, and the stripping recovery of the rare earth can reach 98% in the extraction stage. The total recoveries of rare earth, nickel and cobalt are 98.9%, 98.4% and 98.5%, respectively.

  2. Enhancement of Electrochemical Stability about Silicon/Carbon Composite Anode Materials for Lithium Ion Batteries

    Directory of Open Access Journals (Sweden)

    Wei Xiao

    2015-01-01

    Full Text Available Silicon/carbon (Si/C composite anode materials are successfully synthesized by mechanical ball milling followed by pyrolysis method. The structure and morphology of the composite are characterized by X-ray diffraction and scanning electron microscopy and transmission electron microscope, respectively. The results show that the composite is composed of Si, flake graphite, and phenolic resin-pyrolyzed carbon, and Si and flake graphite are enwrapped by phenolic resin-pyrolyzed carbon, which can provide not only a good buffering matrix but also a conductive network. The Si/C composite also shows good electrochemical stability, in which the composite anode material exhibits a high initial charge capacity of 805.3 mAh g−1 at 100 mA g−1 and it can still deliver a high charge capacity of 791.7 mAh g−1 when the current density increases to 500 mA g−1. The results indicate that it could be used as a promising anode material for lithium ion batteries.

  3. Bismuth Nanoparticles Embedded in Carbon Spheres as Anode Materials for Sodium/Lithium-Ion Batteries.

    Science.gov (United States)

    Yang, Fuhua; Yu, Fan; Zhang, Zhian; Zhang, Kai; Lai, Yanqing; Li, Jie

    2016-02-12

    Sodium-ion batteries (SIBs) are regarded as an attractive alternative to lithium-ion batteries (LIBs) for large-scale commercial applications, because of the abundant terrestrial reserves of sodium. Exporting suitable anode materials is the key to the development of SIBs and LIBs. In this contribution, we report on the fabrication of Bi@C microspheres using aerosol spray pyrolysis technique. When used as SIBs anode materials, the Bi@C microsphere delivered a high capacity of 123.5 mAh g(-1) after 100 cycles at 100 mA g(-1) . The rate performance is also impressive (specific capacities of 299, 252, 192, 141, and 90 mAh g(-1) are obtained under current densities of 0.1, 0.2, 0.5, 1, and 2 A g(-1) , respectively). Furthermore, the Bi@C microsphere also proved to be suitable LIB anode materials. The excellent electrochemical performance for both SIBs and LIBs can attributed to the Bi@C microsphere structure with Bi nanoparticles uniformly dispersed in carbon spheres. PMID:26757402

  4. Preparation and characterization of Li2Mo0.9La0.2O4 anode material

    Institute of Scientific and Technical Information of China (English)

    MO Zunli; CHEN Hong; SUN Yaling; LIU Yanzhi; LI Hejun; LIU Yongzhong

    2006-01-01

    La-doped Li2Mo0.9La0.2O4 was synthesized as an active anode material via the sol-gel process. The structural and morphological characteristics of the target product and the precursor were analyzed by XRD, SEM, and TG-DTA. Crystal started to format at 300℃ and the optimum crystal structure was obtained at 700℃. By detecting battery performance, the charged and discharged platform was over 3.6 V; the anode exhibited a discharge capacity decay of 2% from its initial capacity (165 mA·h/g) after 20 cycles. Therefore, it was a perfect anode material.

  5. Carbon matrix/SiNWs heterogeneous block as improved reversible anodes material for lithium ion batteries

    Institute of Scientific and Technical Information of China (English)

    Yao; Wang; Long; Ren; Yundan; Liu; Xuejun; Liu; Kai; Huang; Xiaolin; Wei; Jun; Li; Xiang; Qi; Jianxin; Zhong

    2014-01-01

    A novel carbon matrix/silicon nanowires(SiNWs) heterogeneous block was successfully produced by dispersing SiNWs into templated carbon matrix via a modified evaporation induced self-assembly method. The heterogeneous block was determined by X-ray diffraction, Raman spectra and scanning electron microscopy. As an anode material for lithium batteries, the block was investigated by cyclic voltammograms(CV), charge/discharge tests, galvanostatic cycling performance and A. C. impedance spectroscopy. We show that the SiNWs disperse into the framework, and are nicely wrapped by the carbon matrix. The heterogeneous block exhibits superior electrochemical reversibility with a high specific capacity of 529.3 mAh/g in comparison with bare SiNWs anode with merely about 52.6 mAh/g capacity retention. The block presents excellent cycle stability and capacity retention which can be attributed to the improvement of conductivity by the existence of carbon matrix and the enhancement of ability to relieve the large volume expansion of SiNWs during the lithium insertion/extraction cycle. The results indicate that the as-prepared carbon matrix/SiNWs heterogeneous block can be an attractive and potential anode material for lithium-ion battery applications.

  6. Electrolytic deposition of Sn-coated mesocarbon microbeads as anode material for lithium ion battery

    Energy Technology Data Exchange (ETDEWEB)

    Deng, Min-Jen [Department of Materials Engineering, National Chung Hsing University, Taichung 40227, Taiwan (China); Jen-Teh Junior College of Medicine, Nursing and Management, Taiwan (China); Tsai, Du-Cheng [Department of Materials Engineering, National Chung Hsing University, Taichung 40227, Taiwan (China); Ho, Wen-Hsien [Taiwan Textile Research Institute, Taipei 23674, Taiwan (China); Li, Ching-Fei, E-mail: chingfei.li@gmail.com [Phoenix Silicon International Corporation, Hsinchu 30094, Taiwan (China); Shieu, Fuh-Sheng, E-mail: fsshieu@dragon.nchu.edu.tw [Department of Materials Engineering, National Chung Hsing University, Taichung 40227, Taiwan (China); Center of Nanoscience and Nanotechnology, National Chung Hsing University, Taichung 40227, Taiwan (China)

    2013-11-15

    Deposited of crystalline tin (Sn) coatings on mesocarbon microbead (MCMB) powder as anodes of lithium ion (Li-ion) battery was conducted in the SnSO{sub 4} solution by a cathodic electrochemical synthesis. The Sn-coated MCMB specimens were characterized by X-ray diffraction, scanning electron microscopy, and charge/discharge tests. The synthesis condition of Sn-coated MCMB was optimized by considering the agglomeration, size, and adhesion of the samples to the current collectors in the battery. The Sn-coated MCMB electrodes exhibit increased reversible capacity without sacrificing its cycling behavior, compared with bare MCMB electrodes. It is concluded that electrolysis-deposited Sn-coated MCMB electrodes may emerge as a practical and promising anode material for secondary Li-ion batteries.

  7. Effects of graphite on Zn-Sb alloys as anode materials for lithium-ion batteries

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    The electrochemical properties of multiphases Zn4Sb3C7 and ZnSbC2 as new lithium-ion anode materials wereinvestigated. The composition and microstructures of these multiphase materials were analyzed by XRD and TEM. It wasfound that the addition of graphite modifies the microstructures of pure alloys. The capacities and the cycle stability of theanodes are greatly improved. The reversible capacity of Zn4Sb3C7 reaches as high as 510 mAh/g at the first cycle, andkeeps higher than 300 mAh/g after 10 charge/discharge cycles

  8. Sol-gel Method Synthesized Polyhedron SnO_2 Anode Material for Lithium Ion Battery

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    1 Introduction Tin-based oxides will be promising anode materials for lithium ion batteries due to its high specific capacity, low potential platform, and safety[1]. Many methods have been applied to synthesize SnO2 materials of different morphologies, such as chemical vapor deposition, spray, sol-gel method[2]. Triblock copolymer poly (ethylene oxide)-block-poly (propylene oxide)-block-poly (ethane oxide) (P123) has been used as surfactant to prepare nano-crystalline tin oxide particles[3]. In this pap...

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

    Science.gov (United States)

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

    2015-03-05

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

  10. Development of high-energy silicon-based anode materials for lithium-ion storage

    Science.gov (United States)

    Yi, Ran

    The emerging markets of electric vehicles (EV) and hybrid electric vehicles (HEV) generate a tremendous demand for low-cost lithium-ion batteries (LIBs) with high energy and power densities, and long cycling life. The development of such LIBs requires development of low cost, high-energy-density cathode and anode materials. Conventional anode materials in commercial LIBs are primarily synthetic graphite-based materials with a capacity of ˜370 mAh/g. Improvements in anode performance, particularly in anode capacity, are essential to achieving high energy densities in LIBs for EV and HEV applications. This dissertation focuses on development of micro-sized silicon-carbon (Si-C) composites as anode materials for high energy and power densities LIBs. First, a new, low-cost, large-scale approach was developed to prepare a micro-sized Si-C composite with excellent performance as an anode material for LIBs. The composite shows a reversible capacity of 1459 mAh/g after 200 cycles at 1 A/g (97.8% capacity retention) and excellent high rate performance of 700 mAh/g at 12.8 A/g, and also has a high tap density of 0.78 g/cm3. The structure of the composite, micro-sized as a whole, features the interconnected nanoscale size of the Si building blocks and the uniform carbon filling, which enables the maximum utilization of silicon even when the micro-sized particles break into small pieces upon cycling. To understand the effects of key parameters in designing the micro-sized Si-C composites on their electrochemical performance and explore how to optimize them, the influence of Si nanoscale building block size and carbon coating on the electrochemical performance of the micro-sized Si-C composites were investigated. It has been found that the critical Si building block size is 15 nm, which enables a high capacity without compromising the cycling stability, and that carbon coating at higher temperature improves the 1st cycle coulombic efficiency (CE) and the rate capability

  11. A new anode material LiMoS2 for use in rechargeable Lithium Ion Batteries

    Institute of Scientific and Technical Information of China (English)

    YANG Shui-jin; AI Chang-chun; LIANG Yong-guang; SUN Ju-tang

    2004-01-01

    The novel applications of molybdenum disulfide in recent research were reviewed, such as in lubricant, catalyst and photoelectrochemical solar cells. Recently, we found that LiMoS2 is a good candidate for new anode materials for lithium ion batteries with high lithium storage capacity.Here, the anode material LiMoS2 was synthesized by a hydrothermal method at 150℃ and the electrochemical characterization as an anode material for lithium ion batteries was examined.put in Teflon-lined stainless steel autoclaves of capacity 40 mL. Distilled water was used to fill the autoclaves to 70 % of the total volume. The autoclaves were maintained at 150℃ for 24 h and then cooled naturally. The resulting dark-gray powders were filled and washed with distilled water,diluted hydrochloric acid and ethanol, successively. The final products were dried at 80℃ for 24 h.The powder X-ray diffraction pattern showed the prepared LiMoS2 was amorphous structure. A test cell using LiMoS2 as the active material was discharged and charged between 3 and 0.01 V with respect to Li metal at a constant current density of C/5 (that is, one lithium per formula unit in 5 hours). During the first discharge, the potential rapidly drops to reach a large plateau at 2.2 V, then slowly drops to the other plateau at 0.8 V, and then continuously decreases down to 0.01V. There is only a plateau at 1.35 V in the subsequent discharge curves. The plateaus of charge potential appear at about 1.9 V.The irreversible loss was 41% in the first cycle. The ratio of discharge and charge is more than 99%in the subsequent cycles. Moreover, the ratio of discharge and charge almost reaches 100% after thedemonstrated that LiMoS2 has a very high capacity and a good cycle-ability as an anode material forlithium ion batteries.

  12. An investigation of oxide composite anode materials for lithium ion batteries

    Science.gov (United States)

    Liu, Bo

    This thesis is aimed to develop high-capacity, inexpensive, long cycle life and environmentally benign anode for lithium-ion batteries. With those goals in mind, a novel oxide alloy composite materials MO-Sn xCoyCz (MO=GeO2, SnO2, SiO and SiO2) have been proposed and investigated. Mechanical alloying method has been used to synthesize oxide alloy composite anode material. The MO-SnxCo yCz composite has the potential to combine the advantageous properties of both Sn-Co-C (long cycle life) and MO (high capacity) and, thereby, improve the overall electrochemical performance. The as-milled materials were studied by BET, laser particle analyzer, X-ray diffraction (XRD), scanning electron microscope (SEM), pair distribution function (PDF), extended X-ray absorption fine structure (EXAFS). Evaluating from electrochemical performance, tap density, and cost, GeO2 and SiO are the most promising candidates alloyed with Sn-Co-C system. The GeO 2 composite anode shows a reversible capacity over 800 mAh/g with good capacity retention. Furthermore, the 1st cycle coulombic efficiency has been improved up to 80%. Compared with GeO2, SiO has an advantage on the price. A series of composite anode materials of xSiO * (1-x)SnxCoyC z were studied by electrochemical method. The composition of 50 wt.%SiO-50 wt.%Sn30Co30C40 shows the best electrochemical performance. Two different milling methods (ultra high-energy milling and SPEX milling) were employed to prepare the samples. Ultra high-energy milling sample exhibited superior electrochemical performance. Stabilized lithium metallic powder technique is employed on this anode to improve the first cycle coulombic efficiency. Full-cell configuration (Li1.2Ni 0.15Co0.10Mn0.55O2 vs. 50 wt.%SiO-50 wt.% Sn30Co30C40) has been cycled over 200 cycles successfully. The SiO-SnxFeyC z (x : y: z molar ratio) composite has been milled in different compositions. Metallic iron was employed instead of cobalt, which cuts the cost significantly but does not

  13. Electrochemical performance of graphene nanosheets as anode material for lithium-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Guo, Peng; Song, Huaihe; Chen, Xiaohong [State Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology, 100029 Beijing (China)

    2009-06-15

    Graphene nanosheets (GNSs) were prepared from artificial graphite by oxidation, rapid expansion and ultrasonic treatment. The morphology, structure and electrochemical performance of GNSs as anode material for lithium-ion batteries were systematically investigated by high-resolution transmission electron microscope, scanning electron microscope, X-ray diffraction, Fourier transform infrared spectroscopy and a variety of electrochemical testing techniques. It was found that GNSs exhibited a relatively high reversible capacity of 672 mA h/g and fine cycle performance. The exchange current density of GNSs increased with the growth of cycle numbers exhibiting the peculiar electrochemical performance. (author)

  14. Methane steam reforming kinetics over Ni-YSZ anode materials for Solid Oxide Fuel Cells

    DEFF Research Database (Denmark)

    Mogensen, David

    of internal reforming has to be carefully controlled. The objective of this thesis is to make such a careful control possible by examining the rate of internal steam reforming in SOFCs. The catalytic steam reforming activity of Ni-YSZ anode material was tested both in a packed bed reactor to determine...... intrinsic kinetics, and in a stack configuration to determine the rate observed under realistic SOFC conditions. The kinetic expressions obtained from respectively the packed bed measurements and the stack measurements are shown in Equations 3 and 4. Furthermore, a simple model was derived, which can...

  15. Orthorhombic Lithium Titanium Phosphate as an Anode Material for Li-ion Rechargeable Battery

    International Nuclear Information System (INIS)

    Highlights: • Li-rich orthorhombic lithium titanium phosphate (OLTP) has been synthesized via a sol-gel route. • OLTP adopts a different space group from the previously reported rhombohedral lithium titanium phosphate (RLTP) and shows solid-solution charge/discharge curves. • OLTP shows higher Li+ diffusivity and electrical conductivity, which makes it an attractive alternative for RLTP. - Abstract: Rhombohedral lithium titanium phosphate, LiTi2(PO4)3, has been considered a suitable anode material for aqueous lithium-ion batteries. However, the electrochemical behaviors of pure lithium-rich polymorphs have not been described yet even Li-rich phase may show better electrochemical properties than conventional LiTi2(PO4)3 at the expense of somewhat lowered capacity. We have synthesized orthorhombic Li1.5Ti2(PO4)3 (OLTP) and rhombohedral LiTi2(PO4)3 (RLTP) via sol-gel reactions and studied their fundamental electrochemical properties using galvanostatic charge/discharge and cyclic voltammetry (CV). Their feasibility as anode materials in LiFePO4//LixTi2(PO4)3 configurations using aqueous electrolytes were also considered. The faster kinetics of the orthorhombic lithium titanium phosphate in this study were attributed to higher Li+ diffusivity and electrical conductivity, making this material an attractive alternative for conventional rhombohedral LiTi2(PO4)3

  16. SYNTHESIS OF NANO-ZnO PARTICLES FOR ALUMINUM METALLURGY AS INERT ANODE MATERIAL

    Institute of Scientific and Technical Information of China (English)

    A.A.A. Saleh; Y. Fu; X.J. Zhai; Y.C. Zhai; M.M. Elomella; A.L. Zhang

    2004-01-01

    Nano-ZnO particle was produced by evaporating zinc powders in air at air flow-rate from 0.2 to 0.6m3/h. Nano-ZnO particles was formed by the oxidation of the evaporated zinc vapor. X-ray diffraction shows the powders to be ZnO with lattice parameters of a=0.3249nm and c=0.5205nm. The particle size is dependent upon the transit time from the source to the collection area. The size of particles was ranged between 81 to 103nm. The average density resulted was 4.865g/cm3.Normal ZnO and nano-ZnO were investigated to use them in aluminum metallurgy as an inert anode material. A certain amount of both oxides were molded subsequently inserted to the molten cryolite-aluminum oxide to investigate the corrosive behavior of both oxides. When the sintering temperature increased up to 1300 ℃, the weight loss ratio rose to 5.01%-7.33% and up to 7.67%-10.18% for nano-ZnO and normal ZnO, respectively. However, when the samples in the molten cryolite aluminum oxide were put for long time, the corrosive rate was found to be higher. It was found that the corrosive loss weight ratio of nano-ZnO anode was much lower than the normal one made from ordinary-ZnO providing that the nano-ZnO is more possible to be use inert anode material.

  17. Surface-modified graphite for improving electrochemical performance of Li-ion battery anode material

    Institute of Scientific and Technical Information of China (English)

    CHEN Jin-ming; WANG Fu-tian; LIU Mao-huang

    2004-01-01

    The graphite materials have been used as negative electrodes in commercial Li-ion batteries for many years. In order to avoid the exfoliation of graphite sheet in the PC-based electrolyte system, it is necessary to make the surface modification on the graphite material. In this study, the electrochemical behavior of carbon-coated graphite in PC-based electrolyte was investigated by charge and discharge cycling process. The carbon-coated graphite can increase the reversible from 366 mA/g to 399mAh/g and improve cycle ability in the PC-based electrolyte system. So the carbon-coated graphite can become the promising high-capacity anode materials of Li-ion battery.

  18. Heat-treated stainless steel felt as scalable anode material for bioelectrochemical systems.

    Science.gov (United States)

    Guo, Kun; Soeriyadi, Alexander H; Feng, Huajun; Prévoteau, Antonin; Patil, Sunil A; Gooding, J Justin; Rabaey, Korneel

    2015-11-01

    This work reports a simple and scalable method to convert stainless steel (SS) felt into an effective anode for bioelectrochemical systems (BESs) by means of heat treatment. X-ray photoelectron spectroscopy and cyclic voltammetry elucidated that the heat treatment generated an iron oxide rich layer on the SS felt surface. The iron oxide layer dramatically enhanced the electroactive biofilm formation on SS felt surface in BESs. Consequently, the sustained current densities achieved on the treated electrodes (1 cm(2)) were around 1.5±0.13 mA/cm(2), which was seven times higher than the untreated electrodes (0.22±0.04 mA/cm(2)). To test the scalability of this material, the heat-treated SS felt was scaled up to 150 cm(2) and similar current density (1.5 mA/cm(2)) was achieved on the larger electrode. The low cost, straightforwardness of the treatment, high conductivity and high bioelectrocatalytic performance make heat-treated SS felt a scalable anodic material for BESs.

  19. Structures, phase stabilities, and electrical potentials of Li-Si battery anode materials

    KAUST Repository

    Tipton, William W.

    2013-05-28

    The Li-Si materials system holds promise for use as an anode in Li-ion battery applications. For this system, we determine the charge capacity, voltage profiles, and energy storage density solely by ab initio methods without any experimental input. We determine the energetics of the stable and metastable Li-Si phases likely to form during the charging and discharging of a battery. Ab initio molecular dynamics simulations are used to model the structure of amorphous Li-Si as a function of composition, and a genetic algorithm coupled to density-functional theory searches the Li-Si binary phase diagram for small-cell, metastable crystal structures. Calculations of the phonon densities of states using density-functional perturbation theory for selected structures determine the importance of vibrational, including zero-point, contributions to the free energies. The energetics and local structural motifs of these metastable Li-Si phases closely resemble those of the amorphous phases, making these small unit cell crystal phases good approximants of the amorphous phase for use in further studies. The charge capacity is estimated, and the electrical potential profiles and the energy density of Li-Si anodes are predicted. We find, in good agreement with experimental measurements, that the formation of amorphous Li-Si only slightly increases the anode potential. Additionally, the genetic algorithm identifies a previously unreported member of the Li-Si binary phase diagram with composition Li5Si2 which is stable at 0 K with respect to previously known phases. We discuss its relationship to the partially occupied Li7Si3 phase. © 2013 American Physical Society.

  20. Evaluation of Al and Some of Its Alloys as Anode Materials vs γ-MnO2 as Cathode Material and Ore Produced γ-MnO2 vs Zn Anode in KOH Solution

    Institute of Scientific and Technical Information of China (English)

    A.M.A.Hashem; Kh.S. Abou-El-Sherbini; S. Zein El Abedin; H. Abbas

    2006-01-01

    In this study electrochemical performance of Al and some of its alloys (Al-Zn, Al-Mg and Al-Mn) anodes vs MnO2 cathode were carried out in alkaline solution. The results show that the Al-Zn alloy anode has the best cell capacity among the other alloys. Cell capacity values go in the order Al-Zn>Al-Mg>Al>Al-Mn. This result is probably related to the nature of passive films formed on the surface of the alloys which examined by scanning electron microscopy (SEM). SEM morphologies of Al and its alloys showed coarse grains of passive films formed on the surface of these anode materials while Al-Mn morphology shows a needle-like structure.Electrolytic manganese dioxide (EMD) produced by electrodepositing on platinum anode from liquor resulting from reduction of low grade pyrolusite ore (β-MnO2) by sulfur slag was characterized as cathode in alkaline Zn-MnO2 batteries. Ore produced sample (EMD1) was performed well in comparison with EMD standard (EMD2) (commercial battery grade electrolytic manganese dioxide, TOSOH-Hellas GH-S). SEM morphology of Zn anode after cell reaction was carried out and showed that Zn anode has fine grains of passive film on its surface.

  1. Electrochemical properties of some cobalt antimonides as anode materials for lithium-ion batteries

    Institute of Scientific and Technical Information of China (English)

    ZHAO Xinbing; CAO Gaoshao; ZHANG Lijuan; XIE Jian

    2003-01-01

    Some cobalt antimonides have been prepared and studied as the candidate anode materials for lithium ion batteries. Reversible capacities of 424, 423 and 546 mA@h@g -1 were measured at the first cycle for as-solidified CoSb2, CoSb3 and annealed CoSb3 respectively. A low lithium ions diffusion coefficient in the order of 10-16 m 2@s -1 was estimated from the coulometric titration measurements in the annealed CoSb3 electrode. It was found that the electrochemical properties of fine powders are significantly better than coarse powders. However the SEM picture shows that the nano-sized CoSb3powders gathered to larger granules, which worsens somewhat the capacity retention of the nano-sized materials, although the volume capacities of the annealed and ball milled CoSb3 remain near twice of that of graphite after 50 cycles.

  2. Preparation and Characterization of Carbon Coated Silicon Nanoparticle as Anode Material for Li-ion Batteries

    Institute of Scientific and Technical Information of China (English)

    T. Zhancg; L.J. Fu; J. Gao; Y. P. Wu; H.Q. Wu

    2005-01-01

    @@ 1Introduction Silicon has been regarded as one of the most promising anode materials for Li-ion batteries. Its theoretical capacity (4 000 mAh/g) is much higher than that of the commercialized graphite (372 mAh/g)[1]. However,the cycle performance of silicon is poor due to the severe volume expansion and shrinkage during Li+ insertion/extraction which results in pulverization of Si particles, eventually losing its Li+ storage ability[2]. To solve this problem, nanosized Si particles were utilized and achieved a partial improvement by reducing the absolute volume change. Nevertheless, a new problem was encountered with nanosized material that small Si particles were aggregated to be larger one during Li+ insertion/extraction, and then pulverized again[3]. In this work, we have succeeded to improve the cycle performance of nanosized Si particles by synthesis of carbon coated silicon nanoparticle.

  3. Novel TiO{sub 2}/C nanocomposites for anode materials of lithium ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Fu, L.J.; Liu, H.; Zhang, H.P.; Li, C.; Zhang, T.; Wu, Y.P.; Wu, H.Q. [Department of Chemistry, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Fudan University, Shanghai 200433 (China)

    2006-09-13

    Here we reported an effective method to prepare TiO{sub 2}/C core-shell nanocomposites as active anode materials for lithium ion batteries with markedly ameliorated electrochemical performance. At first, a precursor, polyacrylonitrile coated nano-TiO{sub 2} particles, was formed by emulsion polymerization. Then the precursor was heat-treated under argon atmosphere to achieve the nanocomposites. The conductive carbon shell enveloped TiO{sub 2} nanoparticles and suppressed the aggregation of nanoparticles during cycling. Meanwhile, it combined closely with the nanocores, significantly enhanced kinetics of lithium intercalation and de-intercalation and diffusion coefficient of lithium ion. This provides a good way to improve the cycling and kinetics of nanoanode materials. (author)

  4. Could Borophene Be Used as a Promising Anode Material for High-Performance Lithium Ion Battery?

    Science.gov (United States)

    Zhang, Yang; Wu, Zhi-Feng; Gao, Peng-Fei; Zhang, Sheng-Li; Wen, Yu-Hua

    2016-08-31

    The rapid development of electronic products has inspired scientists to design and explore novel electrode materials with an ultrahigh rate of charging/discharging capability, such as two-dimensional (2-D) nanostructures of graphene and MoS2. In this study, another 2-D nanosheet, that is a borophene layer, has been predicted to be utilized as a promising anode material for high-performance Li ion battery based on density functional theory calculations. Our study has revealed that Li atom can combine strongly with borophene surface strongly and easily, and exist as a pure Li(+) state. A rather small energy barrier (0.007 eV) of Li diffusion leads to an ultrahigh diffusivity along an uncorrugated direction of borophene, which is estimated to be 10(4) (10(5)) times faster than that on MoS2 (graphene) at room temperature. A high Li storage capacity of 1239 mA·h/g can be achieved when Li content reaches 0.5. A low average operating voltage of 0.466 V and metallic properties result in that the borophene can be used as a possible anode material. Moreover, the properties of Li adsorption and diffusion on the borophene affected by Ag (111) substrate have been studied. It has been found that the influence of Ag (111) substrate is very weak. Li atom can still bind on the borophene with a strong binding energy of -2.648 eV. A small energy barrier of 0.033 eV can be retained for Li diffusion along the uncorrugated direction, which can give rise to a high Li diffusivity. Besides, the performances of borophene-based Na ion battery have been explored. Our results suggest that an extremely high rate capability could be expected in borophene-based Li ion battery. PMID:27487298

  5. Composit, Nanoparticle-Based Anode material for Li-ion Batteries Applied in Hybrid Electric (HEV's)

    Energy Technology Data Exchange (ETDEWEB)

    Dr. Malgorzata Gulbinska

    2009-08-24

    Lithium-ion batteries are promising energy storage devices in hybrid and electric vehicles with high specific energy values ({approx}150 Wh/kg), energy density ({approx}400 Wh/L), and long cycle life (>15 years). However, applications in hybrid and electric vehicles require increased energy density and improved low-temperature (<-10 C) performance. Silicon-based anodes are inexpensive, environmentally benign, and offer excellent theoretical capacity values ({approx}4000 mAh/g), leading to significantly less anode material and thus increasing the overall energy density value for the complete battery (>500 Wh/L). However, tremendous volume changes occur during cycling of pure silicon-based anodes. The expansion and contraction of these silicon particles causes them to fracture and lose electrical contact to the current collector ultimately severely limiting their cycle life. In Phase I of this project Yardney Technical Products, Inc. proposed development of a carbon/nano-silicon composite anode material with improved energy density and silicon's cycleability. In the carbon/nano-Si composite, silicon nanoparticles were embedded in a partially-graphitized carbonaceous matrix. The cycle life of anode material would be extended by decreasing the average particle size of active material (silicon) and by encapsulation of silicon nanoparticles in a ductile carbonaceous matrix. Decreasing the average particle size to a nano-region would also shorten Li-ion diffusion path and thus improve rate capability of the silicon-based anodes. Improved chemical inertness towards PC-based, low-temperature electrolytes was expected as an additional benefit of a thin, partially graphitized coating around the active electrode material.

  6. 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.

  7. Efficient Natural Dye-Sensitized Solar Cells Based on Spin-Coated TiO2 Anode Materials

    Science.gov (United States)

    Yu, Xiao-Hong; Sun, Zhao-Zong; Lian, Jie; Li, Yi-Tan; Chen, Yan-Xue; Gao, Shang; Wang, Xiao; Wang, Ying-Shun; Zhao, Ming-Lin

    2013-11-01

    TiO2 anode materials are prepared on ITO glass by spin-coated method. Dye-sensitized solar cells are assembled with these anodes and natural dyes extracted from radix ophiopogonis by different solvents. The formation and characterization of anode materials are confirmed by field-emission scanning electron microscopy, x-ray diffraction, UV-visible absorption spectroscopy. Photovoltaic testing results show that energy conversion efficiency could reach 1.67% with fill factor of 0.51, open-circuit voltage of 457 mV, and short-circuit photocurrent density of 7.2 mA/cm2. The short-circuit photocurrent density can reach 7.6 mA/cm2 with efficiency of 1.33.

  8. Mechanism of lithium insertion into NiSi2 anode material for lithium ion batteries

    Institute of Scientific and Technical Information of China (English)

    WEN Zhongsheng; JI Shijun; SUN Juncai; TIAN Feng; TIAN Rujin; XIE Jingying

    2006-01-01

    As a promising high capacity anode material for lithium ion batteries, the lithium insertion performance and possible insertion mechanism of binary alloy of NiSi2 were discussed. The initial lithium insertion of crystal NiSi2 can reach up to 600 mAh·g-1 , but large irreversible capacity occurrs simultaneously for serious structure transformation and the irreversible phase forms. XRD and XPS were employed to detect the crystal structure and composition changes produced by lithium insertion. The lithium insertion-extraction behavior of NiSi2 electrode is similar to that of silicon after the first discharge. The structure stability seems related to the non-stoichimometric Ni-Si compound formed by lithium insertion into NiSi2.

  9. Dead lithium phase investigation of Sn-Zn alloy as anode materials for lithium ion battery

    Institute of Scientific and Technical Information of China (English)

    HUANG ZhaoWen; HU SheJun; HOU XianHua; RU Qiang; YU HongWen; ZHAO LingZhi; LI WeiShan

    2009-01-01

    In this work, based on First-principle plane wave pseudo-potential method, we have carried out an in-depth study on the possible dead lithium phase of Sn-Zn alloy as anode materials for lithium ion batteries. Through investigation, we found that the phases LixSn4Zn4(x = 2, 4, 6, 8) contributed to reversible capacity, while the phases LixSn4Zns-(x-4)(x = 4.74, 7.72) led to capacity loss due to high formation energy, namely, they were the dead lithium phases during the charge/discharge process. And we come up with a new idea that stable lithium alloy phase with high lithiation formation energy (dead lithium phase) can also result in high loss of active lithium ion, besides the traditional expression that the formation of solid electrolyte interface film leads to high capacity loss.

  10. Mono-layer BC2 a high capacity anode material for Li-ion batteries

    Science.gov (United States)

    Hardikar, Rahul; Samanta, Atanu; Han, Sang Soo; Lee, Kwang-Ryeol; Singh, Abhishek

    2015-04-01

    Mono-layer of graphene with high surface area compared to the bulk graphite phase, shows less Li uptake. The Li activity or kinetics can be modified via defects and/or substitutional doping. Boron and Nitrogen are the best known dopants for carbonaceous anode materials. In particular, boron doped graphene shows higher capacity and better Li adsorption compared to Nitrogen doped graphene. Here, using first principles density functional theory calculations, we study the spectrum of boron carbide (BCx) mono-layer phases in order to estimate the maximum gravimetric capacity that can be achieved by substitutional doping in graphene. Our results show that uniformly boron doped BC2 phase shows a high capacity of? 1400 mAh/g, much higher than previously reported capacity of BC3. Supported by Korea Institute of Science and Technology.

  11. Defective graphene as promising anode material for Na-ion battery and Ca-ion battery

    CERN Document Server

    Datta, Dibakar; Shenoy, Vivek B

    2013-01-01

    We have investigated adsorption of Na and Ca on graphene with divacancy (DV) and Stone-Wales (SW) defect. Our results show that adsorption is not possible on pristine graphene. However, their adsorption on defective sheet is energetically favorable. The enhanced adsorption can be attributed to the increased charge transfer between adatoms and underlying defective sheet. With the increase in defect density until certain possible limit, maximum percentage of adsorption also increases giving higher battery capacity. For maximum possible DV defect, we can achieve maximum capacity of 1459 mAh/g for Na-ion batteries (NIBs) and 2900 mAh/g for Ca-ion batteries (CIBs). For graphene full of SW defect, we find the maximum capacity of NIBs and CIBs is around 1071 mAh/g and 2142 mAh/g respectively. Our results will help create better anode materials with much higher capacity and better cycling performance for NIBs and CIBs.

  12. Properties and microstructure of NiO/SDC materials for SOFC anode applications

    Institute of Scientific and Technical Information of China (English)

    CHENG Jigui; DENG Liping; ZHANG Benrui; SHI Ping; MENG Guangyao

    2007-01-01

    NiO/SDC composites and Ni/SDC cermets for solid oxide fuel cell (SOFC) anode applications were prepared from nickel oxide (NiO) and samaria doped ceria (SDC) powders by the powder metallurgy process. The physical and mechanical properties, as well as the microstructure of the NiO/SDC composites and the Ni/SDC cermets were investigated. It is shown that the sintering temperature of the NiO/SDC composites and NiO content plays an important role in determining the microstructure and properties of the NiO/SDC composites, which, in turn, influences the microstructure, electrical conductivity, and mechanical properties of the Ni/SDC cermets. The present study demonstrated that composition and tprocess parameters must be appropriately selected to optimize the microstructure and the properties of NiO/SDC materials for solid oxide fuel cell applications.

  13. Electrodeposited gold nanoparticles on carbon nanotube-textile: Anode material for glucose alkaline fuel cells

    KAUST Repository

    Pasta, Mauro

    2012-06-01

    In the present paper we propose a new anode material for glucose-gluconate direct oxidation fuel cells prepared by electrodepositing gold nanoparticles onto a conductive textile made by conformally coating single walled carbon nanotubes (SWNT) on a polyester textile substrate. The electrodeposition conditions were optimized in order to achieve a uniform distribution of gold nanoparticles in the 3D porous structure of the textile. On the basis of previously reported studies, the reaction conditions (pH, electrolyte composition and glucose concentration) were tuned in order to achieve the highest oxidation rate, selectively oxidizing glucose to gluconate. The electrochemical characterization was carried out by means of cyclic voltammetry. © 2012 Elsevier B.V. All rights reserved.

  14. Nitrogen-rich graphene from small molecules as high performance anode material.

    Science.gov (United States)

    Gao, Weiwei; Huang, Hao; Shi, Hongyan; Feng, Xun; Song, Wenbo

    2014-10-17

    Nitrogen-rich graphene sheets were successfully achieved via facile thermal condensation of glucose and dicyandiamide at different temperatures during which dicyandiamide acts both as nitrogen source and sacrifice template. Devoid of surfactants or poisonous organic solvents, this small-molecule synthetic approach is a simple and cost-effective way to obtain nitrogen-rich graphene sheets (NRGS) with high specific surface area and large pore volume. Shown to be a promising anode material, the NRGS displayed high reversible capacity, excellent rate capability, and superior cycle performance. The superior lithium-storage performance is ascribed to the unique features of NRGS, including a large quantity of defects due to the high nitrogen doping level, favorable lithium ion transportation channels by virtue of the large surface area, and ultrahigh pore volume, as well as the crumpled two-dimensional structure.

  15. Effect of the synthesis method of SnSb anode materials on their electrochemical properties

    Institute of Scientific and Technical Information of China (English)

    Chaoli Yin; Hailei Zhao; Hong Guo; Xianliang Huang; Weihua Qiu

    2007-01-01

    SnSb alloy powders for the anode of Li-ion batteries were synthesized by two kinds of reduction precipitation methods:solution titration and rapid mixing. Two kinds of SnSb alloy powders showed different phase compositions and particle morphologies although the same starting materials were used. The SnSb alloy electrode synthesized by titration exhibits high reversible specific capacity and good cycling stability, whereas the rapid-mixing sample shows high irreversible capacity and fast capacity fade. The broad particle size distribution of SnSb powders synthesized by titration is considered to be responsible for the improvement of cycling stability. The initial charge-discharge efficiency exceeding 80% has been obtained for the titration sample. The electrochemical reaction process of two kinds of synthesized SnSb composite electrodes was characterized by cyclic voltammetry and AC impedance techniques.

  16. 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.

  17. Anode materials for hydrogen sulfide containing feeds in a solid oxide fuel cell

    Science.gov (United States)

    Roushanafshar, Milad

    SOFCs which can directly operate under high concentration of H2S would be economically beneficial as this reduces the cost of gas purification. H2S is highly reactive gas specie which can poison most of the conventional catalysts. As a result, developing anode materials which can tolerate high concentrations of H2S and also display high activity toward electrochemical oxidation of feed is crucial and challenging for this application. The performance of La0.4Sr0.6TiO3+/-delta -Y0.2Ce0.8O2-delta (LST-YDC) composite anodes in solid oxide fuel cells significantly improved when 0.5% H2 S was present in syngas (40% H2, 60% CO) or hydrogen. Gas chromatography and mass spectrometry analyses revealed that the rate of electrochemical oxidation of all fuel components improved when H2S containing syngas was present in the fuel. Electrochemical stability tests performed under potentiostatic condition showed that there was no power degradation for different feeds, and that there was power enhancement when 0.5% H2S was present in various feeds. The mechanism of performance improvement by H2S was discussed. Active anodes were synthesized via wet chemical impregnation of different amounts of La0.4Ce0.6O1.8 (LDC) and La 0.4Sr0.6TiO3 (L4ST) into porous yttria-stabilized zirconia (YSZ). Co-impregnation of LDC with LS4T significantly improved the performance of the cell from 48 mW.cm-2 (L4ST) to 161 mW.cm -2 (LDC-L4ST) using hydrogen as fuel at 900 °C. The contribution of LDC to this improvement was investigated using electrochemical impedance spectroscopy (EIS), scanning electron microscopy (SEM) as well as transmission electron microscopy (TEM). EIS measurements using symmetrical cells showed that the polarization resistance decreased from 3.1¦O.cm 2 to 0.5 O.cm2 when LDC was co-impregnated with LST, characterized in humidified H2 (3% H2O) at 900 °C. In addition, the microstructure of the cell was modified when LDC was impregnated prior to L4ST into the porous YSZ. TEM and SEM

  18. Sodium Titanium Phosphate as Anode Materials for Aqueous Sodium-ion Batteries

    Science.gov (United States)

    Wu, Wei

    Renewable energy technology has become one of the promising energy solutions in the future. However, limited by their cyclic behavior, large scale energy storage devices are needed to boost their adoptions in the market. The existing energy storage technologies have limitations that inhibit their adoptions for large scale applications. Our group suggests that one reasonable technology that might overcome these issues is the neutral pH aqueous electrolyte sodium-ion battery. One potential anode material is NaTi2(PO4)3, which has a relatively flexible NASICON skeleton structure and is known in general to have stable performance characteristics in extreme environments. In this work, there are four objectives to study this potential anode material: 1) Develop a rapid method to synthesize electrochemically functional NaTi2(PO4)3. In this case "Electrochemically functional" means the material can store usable capacity for practical application in a composite electrode. 2) Quantify the effect of intimate carbon on NaTi2(PO4)3 electrochemical functionality. (Electrochemical functionality regards the capacity and rate capability of electrode materials) 3) Investigate the stability of NaTi2(PO 4)3 in pH and thermal extremes and the mechanism of capacity fading under different cycling conditions. 4) Examine the performance of NaTi 2(PO4)3 in high salt concentration electrolyte and Li+ electrolyte. NaTi2(PO4)3 has been successfully synthesized via a rapid microwave method. The highest specific capacity is around 85mAh/g has been demonstrated. The effect of different carbon materials (namely graphite and carbon nanotubes) and different processes of adding them (pre and post- synthesis) on the electrochemical performance for sodium titanium phosphate has been extensively studied. Graphite coated NaTi2(PO4) 3 with carbon nanotubes composite electrode has demonstrated a specific capacity of 130mAh/g around theoretical value at 0.1C rate. The effect of the electrolyte (with

  19. Green synthesis of boron doped graphene and its application as high performance anode material in Li ion battery

    Energy Technology Data Exchange (ETDEWEB)

    Sahoo, Madhumita; Sreena, K.P.; Vinayan, B.P.; Ramaprabhu, S., E-mail: ramp@iitm.ac.in

    2015-01-15

    Graphical abstract: Boron doped graphene (B-G), synthesized by simple hydrogen induced reduction technique using boric acid as boron precursor, have more uneven surface as a result of smaller bonding distance of boron compared to carbon, showed high capacity and high rate capability compared to pristine graphene as an anode material for Li ion battery application. - Abstract: The present work demonstrates a facile route for the large-scale, catalyst free, and green synthesis approach of boron doped graphene (B-G) and its use as high performance anode material for Li ion battery (LIB) application. Boron atoms were doped into graphene framework with an atomic percentage of 5.93% via hydrogen induced thermal reduction technique using graphite oxide and boric acid as precursors. Various characterization techniques were used to confirm the boron doping in graphene sheets. B-G as anode material shows a discharge capacity of 548 mAh g{sup −1} at 100 mA g{sup −1} after 30th cycles. At high current density value of 1 A g{sup −1}, B-G as anode material enhances the specific capacity by about 1.7 times compared to pristine graphene. The present study shows a simplistic way of boron doping in graphene leading to an enhanced Li ion adsorption due to the change in electronic states.

  20. Synthesis and electrochemical characterization of Silicon clathrates as anode materials for Lithium ion batteries

    Science.gov (United States)

    Raghavan, Rahul

    Novel materials for Li-ion batteries is one of the principle thrust areas for current research in energy storage, more so than most, considering its widespread use in portable electronic gadgets and plug-in electric and hybrid cars. One of the major limiting factors in a Li-ion battery's energy density is the low specific capacities of the active materials in the electrodes. In the search for high-performance anode materials for Li-ion batteries, many alternatives to carbonaceous materials have been studied. Both cubic and amorphous silicon can reversibly alloy with lithium and have a theoretical capacity of 3500 mAh/g, making silicon a potential high density anode material. However, a large volume expansion of 300% occurs due to changes in the structure during lithium insertion, often leading to pulverization of the silicon. To this end, a class of silicon based cage compounds called clathrates are studied for electrochemical reactivity with lithium. Silicon-clathrates consist of silicon covalently bonded in cage structures comprised of face sharing Si20, Si24 and/or Si28 clusters with guest ions occupying the interstitial positions in the polyhedra. Prior to this, silicon clathrates have been studied primarily for their superconducting and thermoelectric properties. In this work, the synthesis and electrochemical characterization of two categories of silicon clathrates - Type-I silicon clathrate with aluminum framework substitution and barium guest ions (Ba8AlxSi46-x) and Type-II silicon clathrate with sodium guest ions (Nax Si136), are explored. The Type-I clathrate, Ba8AlxSi46-x consists of an open framework of aluminium and silicon, with barium (guest) atoms occupying the interstitial positions. X-ray diffraction studies have shown that a crystalline phase of clathrate is obtained from synthesis, which is powdered to a fine particle size to be used as the anode material in a Li-ion battery. Electrochemical measurements of these type of clathrates have shown

  1. Electrical and Mechanical Performance of Carbon Fiber-Reinforced Polymer Used as the Impressed Current Anode Material

    Directory of Open Access Journals (Sweden)

    Ji-Hua Zhu

    2014-07-01

    Full Text Available An investigation was performed by using carbon fiber-reinforced polymer (CFRP as the anode material in the impressed current cathodic protection (ICCP system of steel reinforced concrete structures. The service life and performance of CFRP were investigated in simulated ICCP systems with various configurations. Constant current densities were maintained during the tests. No significant degradation in electrical and mechanical properties was found for CFRP subjected to anodic polarization with the selected applied current densities. The service life of the CFRP-based ICCP system was discussed based on the practical reinforced concrete structure layout.

  2. Synthesis and characterization of SnO-carbon nanotube composite as anode material for lithium-ion batteries

    International Nuclear Information System (INIS)

    SnO-carbon nanotube composite was synthesized by a sol-gel method. The electrochemical behavior of the composite using an anode active material in lithium-ion batteries was investigated. It was found that the composite showed enhanced anode performance compared with the unsupported SnO or carbon nanotube (CNT). The capacity fade of the composite electrode was reduced over unsupported SnO or CNT. We attribute the results to the conductivity and ductility of the CNT matrix, and the high dispersion of SnO

  3. Dual-carbon enhanced silicon-based composite as superior anode material for lithium ion batteries

    Science.gov (United States)

    Wang, Jie; Liu, Dai-Huo; Wang, Ying-Ying; Hou, Bao-Hua; Zhang, Jing-Ping; Wang, Rong-Shun; Wu, Xing-Long

    2016-03-01

    Dual-carbon enhanced Si-based composite (Si/C/G) has been prepared via employing the widely distributed, low-cost and environmentally friendly Diatomite mineral as silicon raw material. The preparation processes are very simple, non-toxic and easy to scale up. Electrochemical tests as anode material for lithium ion batteries (LIBs) demonstrate that this Si/C/G composite exhibits much improved Li-storage properties in terms of superior high-rate capabilities and excellent cycle stability compared to the pristine Si material as well as both single-carbon modified composites. Specifically for the Si/C/G composite, it can still deliver a high specific capacity of about 470 mAh g-1 at an ultrahigh current density of 5 A g-1, and exhibit a high capacity of 938 mAh g-1 at 0.1 A g-1 with excellent capacity retention in the following 300 cycles. The significantly enhanced Li-storage properties should be attributed to the co-existence of both highly conductive graphite and amorphous carbon in the Si/C/G composite. While the former can enhance the electrical conductivity of the obtained composite, the latter acts as the adhesives to connect the porous Si particulates and conductive graphite flakes to form robust and stable conductive network.

  4. New Sn-based composites as anode materials for Li-ion batteries

    Science.gov (United States)

    Aboulaich, A.; Mouyane, M.; Robert, F.; Lippens, P.-E.; Olivier-Fourcade, J.; Willmann, P.; Jumas, J.-C.

    A new strategy was developed to synthesize tin-composite materials. The Sn:BPO 4 and Sn:CaSiO 3 composites were obtained by solid state reaction, but the BPO 4 and CaSiO 3 matrices were synthesized by solid state reaction and sol-gel method, respectively. These materials are characterized by X-ray diffraction, 119Sn Mössbauer spectroscopy and electrochemical tests. The results show that these new materials are efficient during electrochemical cycling (500 mAh g -1), because of a good dispersion of Sn particles into the matrix. From the second cycle, charge and discharge reversibility is linked to both reversible Li XSn alloy forming and the modification of the tin particle surface showed by Conversion Electron Mössbauer spectroscopy (CEMS) which allows us to characterize the sample surface. The irreversible capacity observed for the first charge/discharge cycle is due to tin oxide reduction and passivation of the anode surface by electrolyte solution decomposition (SEI layer).

  5. Caramel popcorn shaped silicon particle with carbon coating as a high performance anode material for Li-ion batteries.

    Science.gov (United States)

    He, Meinan; Sa, Qina; Liu, Gao; Wang, Yan

    2013-11-13

    Silicon is a very promising anode material for lithium ion batteries. It has a 4200 mAh/g theoretical capacity, which is ten times higher than that of commercial graphite anodes. However, when lithium ions diffuse to Si anodes, the volume of Si will expand to almost 400% of its initial size and lead to the crack of Si. Such a huge volume change and crack cause significant capacity loss. Meanwhile, with the crack of Si particles, the conductivity between the electrode and the current collector drops. Moreover, the solid electrolyte interphase (SEI), which is generated during the cycling, reduces the discharge capacity. These issues must be addressed for widespread application of this material. In this work, caramel popcorn shaped porous silicon particles with carbon coating are fabricated by a set of simple chemical methods as active anode material. Si particles are etched to form a porous structure. The pores in Si provide space for the volume expansion and liquid electrolyte diffusion. A layer of amorphous carbon is formed inside the pores, which gives an excellent isolation between the Si particle and electrolyte, so that the formation of the SEI layer is stabilized. Meanwhile, this novel structure enhances the mechanical properties of the Si particles, and the crack phenomenon caused by the volume change is significantly restrained. Therefore, an excellent cycle life under a high rate for the novel Si electrode is achieved. PMID:24111737

  6. Ultrathin Li4Ti5O12 nanosheets as anode materials for lithium and sodium storage

    Energy Technology Data Exchange (ETDEWEB)

    Feng, Xuyong; Zou, Hailin; Xiang, Hongfa; Guo, Xin; Zhou, Tianpei; Wu, Yucheng; Xu, Wu; Yan, Pengfei; Wang, Chong M.; Zhang, Jiguang; Yu, Yan

    2016-06-13

    Two-dimensional Li4Ti5O12 (LTO) nanosheets are prepared via a surfactant assisted hydrothermal process. Polyether (P123) was added as the surfactant to modify the surface and control the microstructure of the hydrothermal products and thus affect the electrochemical performance of the as-synthesized LTO anode material. XRD results show that the addition of P123 can restrain the growth of Li2TiO3 during the hydrothermal process, thus affecting the morphology and enhancing the rate performance of the final products. With the addition of P123, the growth of LTO can be restrained and ultrathin LTO nanosheets can be obtained after high temperature sintering, which is beneficial for the charge transfer and Li+ ion diffusion. The rate performance of these two different LTO materials is very different because of their differences in phase composition and fine morphology. The P123-assisted nanostructured LTO sample (P-LTO) shows a much higher rate capability than the LTO sample without P123, with over 130 mAh g-1 capacity retained at the charge-discharge rate of 64C when used in a lithium battery. For intercalation of larger size Na+ ions, the P-LTO still exhibit a capacity of 115 mAh g-1 at a charge (de-sodiation process) rate of 10C and maintains 96% capacity after 400 cycles

  7. Centrifugally-spun carbon microfibers and porous carbon microfibers as anode materials for sodium-ion batteries

    Science.gov (United States)

    Dirican, Mahmut; Zhang, Xiangwu

    2016-09-01

    Natural abundance and low cost of sodium resources bring forward the sodium-ion batteries as a promising alternative to widely-used lithium-ion batteries. However, insufficient energy density and low cycling stability of current sodium-ion batteries hinder their practical use for next-generation smart power grid and stationary storage applications. Electrospun carbon microfibers have recently been introduced as a high-performance anode material for sodium-ion batteries. However, electrospinning is not feasible for mass production of carbon microfibers due to its complex processing condition, low production rate and high cost. Herein, we report centrifugal spinning, a high-rate and low-cost microfiber production method, as an alternative approach to electrospinning for carbon microfiber production and introduce centrifugally-spun carbon microfibers (CMFs) and porous carbon microfibers (PCMFs) as anode materials for sodium-ion batteries. Electrochemical performance results indicated that the highly porous nature of centrifugally-spun PCMFs led to increased Na+ storage capacity and improved cycling stability. The reversible capacity of centrifugally-spun PCMF anodes at the 200th cycle was 242 mAh g-1, which was much higher than that of centrifugally-spun CMFs (143 mAh g-1). The capacity retention and coulombic efficiency of the centrifugally-spun PCMF anodes were 89.0% and 99.9%, respectively, even at the 200th cycle.

  8. Tin-based anode materials with well-designed architectures for next-generation lithium-ion batteries

    Science.gov (United States)

    Liu, Lehao; Xie, Fan; Lyu, Jing; Zhao, Tingkai; Li, Tiehu; Choi, Bong Gill

    2016-07-01

    Tin (Sn) has long been considered to be a promising replacement anode material for graphite in next-generation lithium-ion batteries (LIBs), because of its attractive comprehensive advantages of high gravimetric/volumetric capacities, environmental benignity, low cost, high safety, etc. However, Sn-based anodes suffer from severe capacity fading resulting mainly from their large volume expansions/contractions during lithiation/delithiation and subsequent pulverization, coalescence, delamination from current collectors, and poor Li+/electron transport. To circumvent these issues, a number of extraordinary architectures from nanostructures to anchored, layered/sandwich, core-shell, porous and even integrated structures have been exquisitely constructed to enhance the cycling performance. To cater for the rapid development of Sn-based anodes, we summarize the advances made in structural design principles, fabrication methods, morphological features and battery performance with focus on material structures. In addition, we identify the associated challenges and problems presented by recently-developed anodes and offer suggestions and perspectives for facilitating their practical implementations in next-generation LIBs.

  9. Facile synthesis of multilayer-like Si thin film as high-performance anode materials for lithium-ion batteries

    Science.gov (United States)

    Wang, Mingxu; Geng, Zhongrong

    2016-05-01

    For the silicon anodes in lithium-ion batteries, it is well known that the enormous volumetric expansion/contraction is also the mainly reason for the capacity fading. In this manuscript, a new kind of Si thin films was prepared with a radio frequency magnetron sputtering method. By using a periodic modulation negative bias on the substrate, a density-modulated multilayer-like silicon thin films with different layer densities were used as anode materials of lithium-ion batteries, and which displayed a high capacity and stable cycling performances. The reason for the charming electrochemical performances may be owned to the particular density modulated microstructure of the Si thin films. It is conjectured that the lower density can as compliant layers and which provided the volume for the higher-density layer expansion in the process of the lithiation/delithiation. In contrast to the conventional silicon anodes, the density modulated microstructure in this work could exploit a new approach to silicon thin-film anode materials with outstanding electrochemical properties and mechanical stability. And these reports may be provide a new way to prepare the Si thin films for the high-energy, safe, and low-cost batteries.

  10. Degradation of 1-hydroxy-2,4-dinitrobenzene from aqueous solutions by electrochemical oxidation: role of anodic material.

    Science.gov (United States)

    Quiroz, Marco A; Sánchez-Salas, José L; Reyna, Silvia; Bandala, Erick R; Peralta-Hernández, Juan M; Martínez-Huitle, Carlos A

    2014-03-15

    Electrochemical oxidation (ECOx) of 1-hydroxy-2,4-dinitrobenzene (or 2,4-dinitrophenol: 2,4-DNP) in aqueous solutions by electrolysis under galvanostatic control was studied at Pb/PbO2, Ti/SnO2, Ti/IrxRuySnO2 and Si/BDD anodes as a function of current density applied. Oxidative degradation of 2,4-DNP has clearly shown that electrode material and the current density applied were important parameters to optimize the oxidation process. It was observed that 2,4-DNP was oxidized at few substrates to CO2 with different results, obtaining good removal efficiencies at Pb/PbO2, Ti/SnO2 and Si/BDD anodes. Trends in degradation way depend on the production of hydroxyl radicals (OH) on these anodic materials, as confirmed in this study. Furthermore, HPLC results suggested that two kinds of intermediates were generated, polyhydroxylated intermediates and carboxylic acids. The formation of these polyhydroxylated intermediates seems to be associated with the denitration step and substitution by OH radicals on aromatic rings, this being the first proposed step in the reaction mechanism. These compounds were successively oxidized, followed by the opening of aromatic rings and the formation of a series of carboxylic acids which were at the end oxidized into CO2 and H2O. On the basis of these information, a reaction scheme was proposed for each type of anode used for 2,4-D oxidation.

  11. Interweaved Si@C/CNTs and CNFs composites as anode materials for Li-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Miao [School of Physics and Telecommunication Engineering, South China Normal University, Guangzhou 510006 (China); Hou, Xianhua, E-mail: houxh@scnu.edu.cn [School of Physics and Telecommunication Engineering, South China Normal University, Guangzhou 510006 (China); Engineering Research Center of Materials and Technology for Electrochemical Energy Storage Ministry of Education, Guangzhou 510006 (China); Wang, Jie; Li, Min [School of Physics and Telecommunication Engineering, South China Normal University, Guangzhou 510006 (China); Hu, Shejun [School of Physics and Telecommunication Engineering, South China Normal University, Guangzhou 510006 (China); Engineering Research Center of Materials and Technology for Electrochemical Energy Storage Ministry of Education, Guangzhou 510006 (China); Shao, Zongping [Nanjing University of Technology, College of Chemistry and Chemical Engineering, Nanjing 210009 (China); Liu, Xiang [Institute of Advanced Materials, Nanjing University of Technology, Nanjing 210009 (China)

    2014-03-05

    Graphical abstract: In summary, a serious of high-energy wet ball milling, closed spray drying and subsequent chemical vapor deposition methods were introduced successfully to fabricated novel Si@C/CNTs and CNFs composites with carbon nanotubes and carbon nanofibres interweaved with carbon coated silicon spherical composites as superior anodes in lithium-ion batteries. The core-shell structure of Si@C composites can accommodate the volume change of electrode during charge and discharge. Meanwhile, the citric acid pyrolyzed carbon was coated on the surface of the silicon perfectly and constructs the connection network of nano silicon particles. Moreover, the carbon nanotubes and carbon nanofibres, which is interweaved with nano-silicon, also allows high electrical conductivity, improved solid–electrolyte interface formation and structural integrity. Compared with pure silicon and Si@C composites, the novel Si@C/CNTs and CNFs composites had the best combination of reversible capacity and cycleablity, and this anode materials exhibited excellent electrochemical performance. The Si/C composite had a fairly high initial discharge capacity of 2168.7 mA h g{sup −1} with an efficiency of 73%, and the discharge capacity of the 50th cycle maintained surprisingly of 1194.9 mA h g{sup −1}. Meanwhile, spray drying and chemical vapor deposition are environmentally friendly, economical, and relatively high-yield method for the production of the Si@C/CNTs and CNFs composites in large quantities. Consequently, the novel Si@C/CNTs and CNFs composite electrodes may be a potential alternative to graphite for high energy density lithium ion batteries. Highlights: • The core/shell structured silicon/carbon composites were prepared by a facile way. • The as-prepared Si@C/CNTs and CNFs composites shows excellent electrochemical performance. • The preparation method has mild experiment conditions and high production rate. • The structure benefited electronic transfer and

  12. Revisiting Surface Modification of Graphite: Dual-Layer Coating for High-Performance Lithium Battery Anode Materials.

    Science.gov (United States)

    Song, Gyujin; Ryu, Jaegeon; Ko, Seunghee; Bang, Byoung Man; Choi, Sinho; Shin, Myoungsoo; Lee, Sang-Young; Park, Soojin

    2016-06-01

    Surface modification of electrode active materials has garnered considerable attention as a facile way to meet stringent requirements of advanced lithium-ion batteries. Here, we demonstrated a new coating strategy based on dual layers comprising antimony-doped tin oxide (ATO) nanoparticles and carbon. The ATO nanoparticles are synthesized via a hydrothermal method and act as electronically conductive/electrochemically active materials. The as-synthesized ATO nanoparticles are introduced on natural graphite along with citric acid used as a carbon precursor. After carbonization, the carbon/ATO-decorated natural graphite (c/ATO-NG) is produced. In the (carbon/ATO) dual-layer coating, the ATO nanoparticles coupled with the carbon layer exhibit unprecedented synergistic effects. The resultant c/ATO-NG anode materials display significant improvements in capacity (530 mA h g(-1) ), cycling retention (capacity retention of 98.1 % after 50 cycles at a rate of C/5), and low electrode swelling (volume expansion of 38 % after 100 cycles) which outperform that of typical graphite materials. Furthermore, a full-cell consisting of a c/ATO-NG anode and an LiNi0.5 Mn1.5 O4 cathode presents excellent cycle retention (capacity retention of >80 % after 100 cycles). We envision that the dual-layer coating concept proposed herein opens a new route toward high-performance anode materials for lithium-ion batteries. PMID:27027583

  13. Gallium phosphide as a new material for anodically bonded atomic sensors

    Directory of Open Access Journals (Sweden)

    Nezih Dural

    2014-08-01

    Full Text Available Miniaturized atomic sensors are often fabricated using anodic bonding of silicon and borosilicate glass. Here we describe a technique for fabricating anodically bonded alkali-metal cells using GaP and Pyrex. GaP is a non-birefringent semiconductor that is transparent at alkali-metal resonance wavelengths, allowing new sensor geometries. GaP also has a higher thermal conductivity and lower He permeability than borosilicate glass and can be anodically bonded below 200 °C, which can also be advantageous in other vacuum sealing applications.

  14. Nano-sized Fe3O4/carbon as anode material for lithium ion battery

    International Nuclear Information System (INIS)

    Nano-sized Fe3O4/carbon material is prepared via a simple citric-nitrate combustion method combining with a hydrothermal carbon coating technique. The synthesized Fe3O4/carbon composite shows a high reversible specific capacity (ca. 850 mAh g−1 at 100 mA g−1; ca. 600 mAh g−1 at 500 mA g−1), good rate-capability as well as superior cycling stability as anode for lithium-ion batteries. The ameliorated electrochemical performance of Fe3O4/carbon electrode is associated to the nano-sized particle feature and the continuous carbon coating layer. The former provides short lithium-ion/electron diffusion distance, while the latter enables the fast electron transport pathways. Besides, the carbon layer can act as a protective component to prevent the active particle Fe3O4 from aggregation and pulverization during the charge/discharge processes. - Highlights: • Nano-sized Fe3O4/C was prepared by a simple citric-nitrate combustion process. • Fe3O4/C particles show core–shell structure. • Fe3O4/C powder displays high specific capacity and good cycling stability. • Fe3O4/C composite exhibits a superior rate-capability

  15. Novel synthesis of tin oxide/graphene aerogel nanocomposites as anode materials for lithium ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Wu, Zheyu [College of Material Science and Engineering, Liaoning Technical University, Fuxin 123000 (China); Energy & Materials Engineering Centre, College of Physics and Materials Science, Tianjin Normal University, Tianjin 300387 (China); Li, Xifei, E-mail: xfli2011@hotmail.com [Energy & Materials Engineering Centre, College of Physics and Materials Science, Tianjin Normal University, Tianjin 300387 (China); Tai, Limin, E-mail: tailimin@163.com [College of Material Science and Engineering, Liaoning Technical University, Fuxin 123000 (China); Song, Haoze; Zhang, Yiyan; Yan, Bo; Fan, Linlin; Shan, Hui [Energy & Materials Engineering Centre, College of Physics and Materials Science, Tianjin Normal University, Tianjin 300387 (China); Li, Dejun, E-mail: dli1961@126.com [Energy & Materials Engineering Centre, College of Physics and Materials Science, Tianjin Normal University, Tianjin 300387 (China)

    2015-10-15

    A novel method of mechanical exfoliation followed by hydrothermal approach was proposed to synthesize the tin oxide/graphene aerogels (SnO{sub 2}/GAs) nanocomposites. Homogeneous distribution of SnO{sub 2} nanocrystals on GAs was confirmed by SEM, XRD and TEM characterization. It was found that optimized exfoliation of the SnS{sub 2} is the key factor to obtain high electrochemical lithiation/delithiation performance of the anodes. The as-prepared SnO{sub 2}/GA nanocomposites exhibited high reversible capacity (up to 1086.7 mAh g{sup −1} after 100 cycles) and excellent cycling stability. The improved rate capability was also obtained, for instance, the reversible capacity at a current density of 800 mA g{sup −1} is over 447.9 mAh g{sup −1}, and then recovered to as high as 784.4 mAh g{sup −1} at a current density of 100 mA g{sup −1}. - Highlights: • A novel approach was employed to synthesize the SnO{sub 2}/GA nanocomposites. • The designed SnO{sub 2}/GAs exhibited high reversible capacity and excellent cycling stability. • The volume change challenge of SnO{sub 2} was markedly alleviated by the GA matrix. • The novel synthesis method can be extended for other materials in lithium ion batteries.

  16. Protein-releasing conductive anodized alumina membranes for nerve-interface materials.

    Science.gov (United States)

    Altuntas, Sevde; Buyukserin, Fatih; Haider, Ali; Altinok, Buket; Biyikli, Necmi; Aslim, Belma

    2016-10-01

    Nanoporous anodized alumina membranes (AAMs) have numerous biomedical applications spanning from biosensors to controlled drug delivery and implant coatings. Although the use of AAM as an alternative bone implant surface has been successful, its potential as a neural implant coating remains unclear. Here, we introduce conductive and nerve growth factor-releasing AAM substrates that not only provide the native nanoporous morphology for cell adhesion, but also induce neural differentiation. We recently reported the fabrication of such conductive membranes by coating AAMs with a thin C layer. In this study, we investigated the influence of electrical stimulus, surface topography, and chemistry on cell adhesion, neurite extension, and density by using PC 12 pheochromocytoma cells in a custom-made glass microwell setup. The conductive AAMs showed enhanced neurite extension and generation with the electrical stimulus, but cell adhesion on these substrates was poorer compared to the naked AAMs. The latter nanoporous material presents chemical and topographical features for superior neuronal cell adhesion, but, more importantly, when loaded with nerve growth factor, it can provide neurite extension similar to an electrically stimulated CAAM counterpart. PMID:27287158

  17. Ordered CoO/CMK-3 nanocomposites as the anode materials for lithium-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Haijiao; Jiao, Zheng [Institute of Nanochemistry and Nanobiology, Shanghai University, Shanghai 200444 (China); Shanghai Applied Radiation Institute, School of Environmental and Chemical Engineering, Shanghai University, Shangda Road 99, Shanghai 200444 (China); Tao, Haihua; Jiang, Yong; Wu, Minghong; Zhao, Bing [Shanghai Applied Radiation Institute, School of Environmental and Chemical Engineering, Shanghai University, Shangda Road 99, Shanghai 200444 (China)

    2010-05-01

    A novel ordered mesoporous carbon hybrid composite, CoO/CMK-3, is prepared by an infusing method using Co(NO{sub 3}){sub 2}.6H{sub 2}O as the cobalt source. The products are characterized by X-ray diffraction, transmission electron microscopy and N{sub 2} adsorption-desorption analysis techniques. It is observed that the CoO nanoparticles are loaded in the channels of mesoporous carbon. The mesopore structure of CMK-3 is destroyed gradually with increasing of the CoO content. The electrochemical properties of samples as the anode materials for lithium-ion batteries are studied by galvanostatic method. The results show that the CoO/CMK-3 composites have higher reversible capacities (more than 700 mAh g{sup -1}) and better cycle performance in comparison with the pure mesoporous carbon (CMK-3). Based on the above results, a mechanism is proposed to explain the reason of such a substantial improvement of electrochemical performance in the CoO/CMK-3 composites. (author)

  18. Improvement of thermal stability and safety of lithium ion battery using SiO anode material

    Science.gov (United States)

    Liu, Yi-Hung; Okano, Miki; Mukai, Takashi; Inoue, Kenshi; Yanagida, Masahiro; Sakai, Tetsuo

    2016-02-01

    The thermal stability, in terms of cycle and rate performances at 80 °C, and its safety related to lithium ion batteries composed of a LiFePO4 cathode and SiO anode are investigated. Based on an STEM-EELS analysis, the SiO powder is found to have an amorphous structure, in which nanosized Si particles (Si-rich phase) are uniformly dispersed in the SiO2 matrix (SiO2-rich phase). During the charge/discharge cycling, the cell exhibits a satisfactory cycle performance with a discharge capacity retention of 93.6% and a voltage retention of 93.9% at the 1500th cycle. Also, the charge and discharge capacity retentions at 10 C are 97.5% and 94.7%, respectively, together with a limited polarization, demonstrating its high rate performance. Furthermore, a 1.16 Ah LiFePO4/SiO laminated cell shows negligible voltage and temperature changes during the nail penetration test. The Li concentration in the active material (Si-rich phase) is found to be almost the same as that in the SiO2-rich phase after the test. This high thermal stability and safety may be due to the formed layer from the SiO2 matrix, preventing any side reaction from occurring on the Si surface and isolating the internal current path during the nail penetration.

  19. Novel synthesis of tin oxide/graphene aerogel nanocomposites as anode materials for lithium ion batteries

    International Nuclear Information System (INIS)

    A novel method of mechanical exfoliation followed by hydrothermal approach was proposed to synthesize the tin oxide/graphene aerogels (SnO2/GAs) nanocomposites. Homogeneous distribution of SnO2 nanocrystals on GAs was confirmed by SEM, XRD and TEM characterization. It was found that optimized exfoliation of the SnS2 is the key factor to obtain high electrochemical lithiation/delithiation performance of the anodes. The as-prepared SnO2/GA nanocomposites exhibited high reversible capacity (up to 1086.7 mAh g−1 after 100 cycles) and excellent cycling stability. The improved rate capability was also obtained, for instance, the reversible capacity at a current density of 800 mA g−1 is over 447.9 mAh g−1, and then recovered to as high as 784.4 mAh g−1 at a current density of 100 mA g−1. - Highlights: • A novel approach was employed to synthesize the SnO2/GA nanocomposites. • The designed SnO2/GAs exhibited high reversible capacity and excellent cycling stability. • The volume change challenge of SnO2 was markedly alleviated by the GA matrix. • The novel synthesis method can be extended for other materials in lithium ion batteries

  20. Electrochemical performance of polygonized carbon nanofibers as anode materials for lithium-ion batteries

    Institute of Scientific and Technical Information of China (English)

    Jinjin Jiang; xiaolin Tang; Rui Wu; Haoqiang Lin; Meizhen Qu

    2013-01-01

    Carbon nanofibers with a polygonal cross section (P-CNFs) synthesized using a catalytic chemical vapor deposition (CCVD) technology have been investigated for potential applications in lithium batteries as anode materials.P-CNFs exhibit excellent high-rate capabilities.At a current density as high as 3.7 and 7.4A/g,P-CNFs can still deliver a reversible capacity of 198.4 and 158.2 mAh/g,respectively.To improve their first coulombic efficiency,carbon-coated P-CNFs were prepared through thermal vapor deposition (TVD) of benzene at 900 ℃.The electrochemical results demonstrate that appropriate amount of carbon coating can improve the first coulombic efficiency,the cycling stability and the rate performance of P-CNFs.After carbon coating,P-CNFs gain a weight increase approximately by 103 wt%,with its first coulombic efficiency increasing from 63.1 to 78.4%,and deliver a reversible capacity of 197.4mAh/g at a current density of 3.7 A/g.After dozens of cycles,there is no significant capacity degradation at both low and high current densities.

  1. Electrospun carbon nanofibers from polyacrylonitrile blended with activated or graphitized carbonaceous materials for improving anodic bioelectrocatalysis.

    Science.gov (United States)

    Patil, Sunil A; Chigome, Samuel; Hägerhäll, Cecilia; Torto, Nelson; Gorton, Lo

    2013-03-01

    The electrospun carbon nanofibers obtained from polyacrylonitrile (PAN) and PAN blends with either activated carbon (PAN-AC) or graphite (PAN-GR) were tested as anodes using Shewanella oneidensis MR-1. Extensive physico-chemical and electrochemical characterization confirmed their formation, their fibrous and porous nature, and their suitability as electrodes. N2 adsorption measurements revealed high specific surface area (229.8, 415.8 and 485.2m(2) g(-1)) and porosity (0.142, 0.202 and 0.239cm(3)g(-1)) for PAN, PAN-AC and PAN-GR, respectively. The chronoamperometric measurements showed a considerable decrease in start-up time and more than a 10-fold increase in the generation of current with these electrodes (115, 139 and 155μAcm(-2) for PAN, PAN-AC and PAN-GR, respectively) compared to the graphite electrode (11.5μAcm(-2)). These results indicate that the bioelectrocatalysis benefits from the blending of PAN with activated or graphitized carbonaceous materials, presumably due to the increased specific surface area, total pore volume and modification of the carbon microstructure. PMID:23399497

  2. Hollow Cobalt Selenide Microspheres: Synthesis and Application as Anode Materials for Na-Ion Batteries.

    Science.gov (United States)

    Ko, You Na; Choi, Seung Ho; Kang, Yun Chan

    2016-03-16

    The electrochemical properties of hollow cobalt oxide and cobalt selenide microspheres are studied for the first time as anode materials for Na-ion batteries. Hollow cobalt oxide microspheres prepared by one-pot spray pyrolysis are transformed into hollow cobalt selenide microspheres by a simple selenization process using hydrogen selenide gas. Ultrafine nanocrystals of Co3O4 microspheres are preserved in the cobalt selenide microspheres selenized at 300 °C. The initial discharge capacities for the Co3O4 and cobalt selenide microspheres selenized at 300 and 400 °C are 727, 595, and 586 mA h g(-1), respectively, at a current density of 500 mA g(-1). The discharge capacities after 40 cycles for the same samples are 348, 467, and 251 mA h g(-1), respectively, and their capacity retentions measured from the second cycle onward are 66, 91, and 50%, respectively. The hollow cobalt selenide microspheres have better rate performances than the hollow cobalt oxide microspheres. PMID:26918934

  3. The electrochemical performance and mechanism of cobalt (II) fluoride as anode material for lithium and sodium ion batteries

    International Nuclear Information System (INIS)

    Highlights: •The as-prepared CoF2 shows excellent electrochemical performance as anode material for lithium ion batteries. •The Li insertion/extraction mechanism of CoF2 below 1.2 V was firstly proposed. •The electrochemical performance of CoF2 as anode material in sodium ion batteries was firstly studied. -- Abstract: Cobalt (II) fluoride begins to enter into the horizons of people along with the research upsurge of metal fluorides. It is very significative and theoretically influential to make certain its electrochemical reaction mechanism. In this work, we discover a new and unrevealed reversible interfacial intercalation mechanism reacting below 1.2 V for cobalt (II) fluoride electrode material, which contributes a combined discharge capacity of about 400 mA h g−1 with the formation of SEI film at the initial discharge process. A highly reversible storage capacity of 120 mA h g−1 is observed when the cell is cycled over the voltage of 0.01-1.2 V at 0.2 C, and the low-potential voltage reaction process has a significant impact for the whole electrochemical process. Electrochemical analyses suggest that pure cobalt (II) fluoride shows better electrochemical performance when it is cycled at 3.2-0.01 V compared to the high range (1.0-4.5 V). So, we hold that cobalt (II) fluoride is more suitable to serve as anode material for lithium ion batteries. In addition, we also try to reveal the relevant performance and reaction mechanism, and realize the possibility of cobalt (II) fluoride as anode material for sodium ion batteries

  4. TiO2 anode materials for lithium-ion batteries with different morphology and additives

    Science.gov (United States)

    Liu, Xiang; Ng, Yip Hang; Leung, Yu Hang; Liu, Fangzhou; Djurišic, Aleksandra B.; Xie, Mao Hai; Chan, Wai Kin

    2014-03-01

    Electrochemical performances of different TiO2 nanostructures, TiO2/CNT composite and TiO2 with titanium isopropoxide (TTIP) treatment anode were investigated. For different TiO2 nanostructures, we investigated vertically aligned TiO2 nanotubes on Ti foil and TiO2 nanotube-powders fabricated by rapid breakdown anodization technique. The morphology of the prepared samples was characterized by scanning probe microscopy (SEM). The electrochemical lithium storage abilities were studied by galvanostatic method. In addition, carbon nanotubes (CNT) additives and solution treatment process of TiO2 anode were investigated, and the results show that the additives and treatment could enhance the cycling performance of the TiO2 anode on lithium ion batteries.

  5. Potential threshold of anode materials for foldable lithium-ion batteries featuring carbon nanotube current collectors

    Science.gov (United States)

    Wang, Qing Hui; Zhong, Sheng Wen; Hu, Jing Wei; Liu, Ting; Zhu, Xian Yan; Chen, Jing; Hong, Yin Yan; Wu, Zi Ping

    2016-04-01

    Flexible carbon nanotube macro-films (CMFs) are perfect current collectors for preparing foldable lithium-ion batteries (LIBs). However, selecting appropriate anodes for electrode is difficult because of the different potentials (vs. Li/Li+) of carbon nanotubes and traditional metallic current collector. This study demonstrated an additional reaction at potential below 0.9 V (vs. Li/Li+) caused by CMF, And Li+ will be constrained, which decreased capacity of anode/CMF electrode. Conversely, results changed when the anode potential exceeded 0.9 V (vs. Li/Li+) because Li+ passed the potential threshold, and the CMF retained its electrochemical inactivity. Consequently, the CMF-based foldable LIBs performed well. The potential threshold mechanism of anode is expected to provide new impetus to both academia and industry for exploring flexible or foldable LIBs.

  6. 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.

  7. Synthesis and Characterization of Silicon Nanoparticles Inserted into Graphene Sheets as High Performance Anode Material for Lithium Ion Batteries

    OpenAIRE

    Yong Chen; Xuejun Zhang; Yanhong Tian; Xi Zhao

    2014-01-01

    Silicon nanoparticles have been successfully inserted into graphene sheets via a novel method combining freeze-drying and thermal reduction. The structure, electrochemical performance, and cycling stability of this anode material were characterized by SEM, X-ray diffraction (XRD), charge/discharge cycling, and cyclic voltammetry (CV). CV showed that the Si/graphene nanocomposite exhibits remarkably enhanced cycling performance and rate performance compared with bare Si nanoparticles for lithi...

  8. Nano Structure Plays an Important Role in the Present and Future Anode Materials of Li-ion Batteries

    Institute of Scientific and Technical Information of China (English)

    Tsutomu; Takamura

    2007-01-01

    1 ResultsLi-ion batteries are the most promising secondary batteries for IT and EV applications, where it is required to increase the capacity and power capability to a great extent. In responding to the demand we have been studied on the anode materials especially paying attention on the improved graphite active materials and modified silicon. In both cases we realized that the nano-structured design plays an important role. In this paper the examples of nano-size structure working in the actual materi...

  9. Kinetics of the electrolytic Fe+2/Fe+3 oxidation on various anode materials

    Directory of Open Access Journals (Sweden)

    Cifuentes, L.

    2003-08-01

    Full Text Available The kinetics of the electrolytic Fe+2/Fe+3 oxidation, relevant to hydro-electrometallurgical processing, have been studied on lead, platinum, ruthenium oxide, iridium oxide and graphite anodes in ferrous sulfate-sulfuric acid solutions. The oxidation rate depends on ferrous sulfate concentration, solution temperature and degree of agitation. Potentiodynamic studies show that: a the highest oxidation rate is obtained on platinum; b lead is unsuitable as anodic material for the said reaction; c the remaining anode materials show a similar and satisfactory performance.

    Se ha estudiado la cinética de la oxidación electrolítica Fe+2/Fe+3 -relevante para el procesamiento hidroelectrometalúrgico- sobre plomo, platino, óxido de rutenio, óxido de iridio y grafito en soluciones de sulfato ferroso en ácido sulfúrico. La velocidad de oxidación depende de la concentración de sulfato ferroso, la temperatura de la solución y el grado de agitación. Estudios potenciodinámicos demuestran que: a las mayores velocidades de oxidación se obtienen sobre platino; b el plomo es inadecuado como material anódico para la reacción mencionada; c los materiales anódicos restantes exhiben un desempeño similar y satisfactorio.

  10. The developments of SnO2/graphene nanocomposites as anode materials for high performance lithium ion batteries: A review

    Science.gov (United States)

    Deng, Yuanfu; Fang, Chengcheng; Chen, Guohua

    2016-02-01

    With the increasing energy demands for electronic devices and electrical vehicles, anode materials for lithium ion batteries (LIBs) with high specific capacity, good cyclic and rate performances become one of the focal areas of research. Among the various anode materials, SnO2/graphene nanocomposites have drawn extensive attentions due to their high theoretical specific capacities, low charge potential vs. Li/Li+ and environmental benignity. In this review, the advances, including the synthetic methods and structural optimizations, of the SnO2/graphene nanocomposites as anode materials for LIBs have been reviewed in detail. By providing an in-depth discussion of SnO2/graphene nanocomposites, we aim to demonstrate that the electrochemical performances of SnO2/graphene nanocomposites could be significantly enhanced by rational modifications of morphology and crystal structures, chemical compositions and surface features. Though only focusing on SnO2/graphene-based composites, the concepts and strategies should be referential to other metal oxide/graphene composites.

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

    Science.gov (United States)

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

    2015-11-11

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

  12. Novel Mg-Doped SrMoO3 Perovskites Designed as Anode Materials for Solid Oxide Fuel Cells

    Directory of Open Access Journals (Sweden)

    Vanessa Cascos

    2016-07-01

    Full Text Available SrMo1−xMxO3−δ (M = Fe and Cr, x = 0.1 and 0.2 oxides have been recently described as excellent anode materials for solid oxide fuel cells at intermediate temperatures (IT-SOFC with LSGM as the electrolyte. In this work, we have improved their properties by doping with aliovalent Mg ions at the B-site of the parent SrMoO3 perovskite. SrMo1−xMgxO3−δ (x = 0.1, 0.2 oxides have been prepared, characterized and tested as anode materials in single solid-oxide fuel cells, yielding output powers near 900 mW/cm−2 at 850 °C using pure H2 as fuel. We have studied its crystal structure with an “in situ” neutron power diffraction (NPD experiment at temperatures as high as 800 °C, emulating the working conditions of an SOFC. Adequately high oxygen deficiencies, observed by NPD, together with elevated disk-shaped anisotropic displacement factors suggest a high ionic conductivity at the working temperatures. Furthermore, thermal expansion measurements, chemical compatibility with the LSGM electrolyte, electronic conductivity and reversibility upon cycling in oxidizing-reducing atmospheres have been carried out to find out the correlation between the excellent performance as an anode and the structural features.

  13. Nanostructured Black Phosphorus/Ketjenblack-Multiwalled Carbon Nanotubes Composite as High Performance Anode Material for Sodium-Ion Batteries.

    Science.gov (United States)

    Xu, Gui-Liang; Chen, Zonghai; Zhong, Gui-Ming; Liu, Yuzi; Yang, Yong; Ma, Tianyuan; Ren, Yang; Zuo, Xiaobing; Wu, Xue-Hang; Zhang, Xiaoyi; Amine, Khalil

    2016-06-01

    Sodium-ion batteries are promising alternatives to lithium-ion batteries for large-scale applications. However, the low capacity and poor rate capability of existing anodes for sodium-ion batteries are bottlenecks for future developments. Here, we report a high performance nanostructured anode material for sodium-ion batteries that is fabricated by high energy ball milling to form black phosphorus/Ketjenblack-multiwalled carbon nanotubes (BPC) composite. With this strategy, the BPC composite with a high phosphorus content (70 wt %) could deliver a very high initial Coulombic efficiency (>90%) and high specific capacity with excellent cyclability at high rate of charge/discharge (∼1700 mAh g(-1) after 100 cycles at 1.3 A g(-1) based on the mass of P). In situ electrochemical impedance spectroscopy, synchrotron high energy X-ray diffraction, ex situ small/wide-angle X-ray scattering, high resolution transmission electronic microscopy, and nuclear magnetic resonance were further used to unravel its superior sodium storage performance. The scientific findings gained in this work are expected to serve as a guide for future design on high performance anode material for sodium-ion batteries.

  14. Nanostructured Black Phosphorus/Ketjenblack-Multiwalled Carbon Nanotubes Composite as High Performance Anode Material for Sodium-Ion Batteries.

    Science.gov (United States)

    Xu, Gui-Liang; Chen, Zonghai; Zhong, Gui-Ming; Liu, Yuzi; Yang, Yong; Ma, Tianyuan; Ren, Yang; Zuo, Xiaobing; Wu, Xue-Hang; Zhang, Xiaoyi; Amine, Khalil

    2016-06-01

    Sodium-ion batteries are promising alternatives to lithium-ion batteries for large-scale applications. However, the low capacity and poor rate capability of existing anodes for sodium-ion batteries are bottlenecks for future developments. Here, we report a high performance nanostructured anode material for sodium-ion batteries that is fabricated by high energy ball milling to form black phosphorus/Ketjenblack-multiwalled carbon nanotubes (BPC) composite. With this strategy, the BPC composite with a high phosphorus content (70 wt %) could deliver a very high initial Coulombic efficiency (>90%) and high specific capacity with excellent cyclability at high rate of charge/discharge (∼1700 mAh g(-1) after 100 cycles at 1.3 A g(-1) based on the mass of P). In situ electrochemical impedance spectroscopy, synchrotron high energy X-ray diffraction, ex situ small/wide-angle X-ray scattering, high resolution transmission electronic microscopy, and nuclear magnetic resonance were further used to unravel its superior sodium storage performance. The scientific findings gained in this work are expected to serve as a guide for future design on high performance anode material for sodium-ion batteries. PMID:27222911

  15. Synthesis of Li2Ti3O7 Anode Materials by Ultrasonic Spray Pyrolysis and Their Electrochemical Properties

    Directory of Open Access Journals (Sweden)

    Takayuki Kodera

    2013-06-01

    Full Text Available Ramsdellite-type lithium titanate (Li2Ti3O7 powders were synthesized by performing ultrasonic spray pyrolysis, and their chemical and physical properties were characterized by performing Scanning Electron Microscope (SEM, powder X-ray Diffraction (XRD, and Inductively Coupled Plasma (ICP analyses. The as-prepared Li2Ti3O7 precursor powders had spherical morphologies with hollow microstructures, but an irregularly shaped morphology was obtained after calcination above 900 °C. The ramsdellite Li2Ti3O7 crystal phase was obtained after the calcination at 1100 °C under an argon/hydrogen atmosphere. The first rechargeable capacity of the Li2Ti3O7 anode material was 168 mAh/g at 0.1 C and 82 mAh/g at 20 C, and the discharge capacity retention ratio was 99% at 1 C after the 500th cycle. The cycle performance of the Li2Ti3O7 anode was also highly stable at 50 °C, demonstrating the superiority of Li2Ti3O7 anode materials reported previously.

  16. Nanoparticle Cookies Derived from Metal-Organic Frameworks: Controlled Synthesis and Application in Anode Materials for Lithium-Ion Batteries.

    Science.gov (United States)

    Wang, Shuhai; Chen, Minqi; Xie, Yanyu; Fan, Yanan; Wang, Dawei; Jiang, Ji-Jun; Li, Yongguang; Grützmacher, Hansjörg; Su, Cheng-Yong

    2016-05-01

    The capacity of anode materials plays a critical role in the performance of lithium-ion batteries. Using the nanocrystals of oxygen-free metal-organic framework ZIF-67 as precursor, a one-step calcination approach toward the controlled synthesis of CoO nanoparticle cookies with excellent anodic performances is developed in this work. The CoO nanoparticle cookies feature highly porous structure composed of small CoO nanoparticles (≈12 nm in diameter) and nitrogen-rich graphitic carbon matrix (≈18 at% in nitrogen content). Benefiting from such unique structure, the CoO nanoparticle cookies are capable of delivering superior specific capacity and cycling stability (1383 mA h g(-1) after 200 runs at 100 mA g(-1) ) over those of CoO and graphite.

  17. Nano-crystalline FeOOH mixed with SWNT matrix as a superior anode material for lithium batteries

    Institute of Scientific and Technical Information of China (English)

    Mingzhong Zou; Weiwei Wen; Jiaxin Li; Yingbin Lin; Heng Lai; Zhigao Huang

    2014-01-01

    Nano-crystalline FeOOH particles (5∼10 nm) have been uniformly mixed with electric matrix of single-walled carbon nanotubes (SWNTs) for forming FeOOH/SWNT composite via a facile ultrasonication method. Directly using the FeOOH/SWNT composite (containing 15 wt%SWNTs) as anode material for lithium battery enhances kinetics of the Li+ insertion/extraction processes, thereby effectively improving re-versible capacity and cycle performance, which delivers a high reversible capacity of 758 mAh·g-1 under a current density of 400 mA·g-1 even after 180 cycles, being comparable with previous reports in terms of electrochemical performance for FeOOH anode. The good electrochemical performance should be ascribed to the small particle size and nano-crystalline of FeOOH, as well as the good electronic conductivity of SWNT matrix.

  18. 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.

  19. Dispersing SnO2 nanocrystals in amorphous carbon as a cyclic durable anode material for lithium ion batteries

    Institute of Scientific and Technical Information of China (English)

    Renzong Hu; Wei Sun; Meiqin Zeng; Min Zhu

    2014-01-01

    We demonstrate a facile route for the massive production of SnO2/carbon nanocomposite used as high-capacity anode materials of next-generation lithium-ion batteries. The nanocomposite had a unique structure of ultrafine SnO2 nanocrystals (∼5 nm, 80 wt%) homogeneously dispersed in amorphous carbon matrix. This structure design can well accommodate the volume change of Li+insertion/desertion in SnO2, and prevent the aggregation of the nanosized active materials during cycling, leading to superior cycle performance with stable reversible capacity of 400 mAh/g at a high current rate of 3.3 A/g.

  20. Pulsed laser deposited Cr2O3 nanostructured thin film on graphene as anode material for lithium-ion batteries

    International Nuclear Information System (INIS)

    Graphical abstract: A different approach for the fabrication of an anode material system that comprises pulsed laser-deposited (PLD) Cr2O3 grown on few layer graphene (FLG) by chemical vapor deposition (CVD) was used. The electrochemical performance of Cr2O3 nanostructured thin film was improved by FLG, which make it a promising candidate for future lithium-ion batteries application. - Highlights: • Pulsed laser deposition technique was used to deposit Cr2O3 on few-layer graphene (FLG). • FLG improved the electrochemical performance of Cr2O3 nanostructured thin film. • Good stable cycle of Cr2O3/FLG/Ni electrode make it one of the promise anode materials for future lithium-ion batteries. - Abstract: Pulsed laser deposition technique was used to deposit Cr2O3 nanostructured thin film on a chemical vapor deposited few-layer graphene (FLG) on nickel (Ni) substrate for application as anode material for lithium-ion batteries. The experimental results show that graphene can effectively enhance the electrochemical property of Cr2O3. For Cr2O3 thin film deposited on Ni (Cr2O3/Ni), a discharge capacity of 747.8 mA h g−1 can be delivered during the first lithiation process. After growing Cr2O3 thin film on FLG/Ni, the initial discharge capacity of Cr2O3/FLG/Ni was improved to 1234.5 mA h g−1. The reversible lithium storage capacity of the as-grown material is 692.2 mA h g−1 after 100 cycles, which is much higher than that of Cr2O3/Ni (111.3 mA h g−1). This study reveals the differences between the two material systems and emphasizes the role of the graphene layers in improving the electrochemical stability of the Cr2O3 nanostructured thin film

  1. Marine microbial fuel cell: Use of stainless steel electrodes as anode and cathode materials

    Energy Technology Data Exchange (ETDEWEB)

    Dumas, C.; Basseguy, R.; Etcheverry, L.; Bergel, A. [Laboratoire de Genie Chimique, CNRS-INPT, Toulouse Cedex (France); Mollica, A. [CNR-ISMAR, Genoa (Italy); Feron, D. [SCCME, CEA Saclay, Gif-sur-Yvette (France)

    2007-12-01

    Numerous biocorrosion studies have stated that biofilms formed in aerobic seawater induce an efficient catalysis of the oxygen reduction on stainless steels. This property was implemented here for the first time in a marine microbial fuel cell (MFC). A prototype was designed with a stainless steel anode embedded in marine sediments coupled to a stainless steel cathode in the overlying seawater. Recording current/potential curves during the progress of the experiment confirmed that the cathode progressively acquired effective catalytic properties. The maximal power density produced of 4 mW m{sup -2} was lower than those reported previously with marine MFC using graphite electrodes. Decoupling anode and cathode showed that the cathode suffered practical problems related to implementation in the sea, which may found easy technical solutions. A laboratory fuel cell based on the same principle demonstrated that the biofilm-covered stainless steel cathode was able to supply current density up to 140 mA m{sup -2} at +0.05 V versus Ag/AgCl. The power density of 23 mW m{sup -2} was in this case limited by the anode. These first tests presented the biofilm-covered stainless steel cathodes as very promising candidates to be implemented in marine MFC. The suitability of stainless steel as anode has to be further investigated. (author)

  2. Fabrication of electrospun ZnMn2O4 nanofibers as anode material for lithium-ion batteries

    International Nuclear Information System (INIS)

    Highlights: • ZnMn2O4 nanofibers were successfully synthesized by a facile electrospinning and calcination method for lithium-ion batteries. • The as-prepared ZnMn2O4 nanofibers, containing PVP and PAN with ratio of 1:9, exhibited a high initial discharge capacity of 1274 mAh g−1, and the stabilized capacity was as high as 603 mAh g−1 after 60 cycles at a current density of 50 mA g−1. • The as-prepared ZnMn2O4 anode material showed good lithium storage performances and excellent rate capability and can be a promising electrode material for lithium-ion batteries in the future. - Abstract: In this paper, ZnMn2O4 nanofibers were synthesized by a facile electrospinning and calcination method. Electrochemical properties of the nanofiber anode material for lithium-ion batteries were investigated. The as-prepared ZnMn2O4 nanofibers, containing PVP and PAN with ratio of 1:9, exhibited a high initial discharge capacity of 1274 mAh g−1, and the stabilized capacity was as high as 603 mAh g−1 after 60 cycles at a current density of 50 mA g−1. Besides the high specific capacity and good cyclability, the electrode also showed good rate capability. Even at 2000 mA g−1, the electrode could deliver a capacity of as high as 352 mAh g−1. The results suggest a promising application of the electrospun ZnMn2O4 nanofibers as anode material for lithium-ion batteries

  3. Synthetic, structural, and electrochemical study of monoclinic Na4Ti5O12 as sodium-ion battery anode material

    International Nuclear Information System (INIS)

    Since lithium-ion batteries were commercialized in 1991, they have dominated the portable electronics market. In 2014, over one-fourth of the world’s mined lithium was devoted to lithiumion battery applications. Increased future demand will be driven by the electric/hybrid vehicle market and load leveling solutions for renewable energy sources. Therefore, the development of new, low-cost alternatives to lithium-ion batteries with comparable electrochemical properties is highly desirable. Sodium is the most obvious choice, as an inexpensive, abundant, and easily extractable element. As well as the decreased cost in starting material, sodium-ion batteries can use aluminum as the current collector for the anode because, unlike lithium, sodium does not alloy with aluminum metal. Aluminum offers both a less-expensive and lighter alternative to the copper usually used in lithium-ion batteries. However, challenges still remain in developing sodium intercalation materials capable of achieving a high reversible capacity and energy density. In particular, because of the inability of Na ions to intercalate with graphite, anode materials must be significantly improved. We have investigated the monoclinic phase of Na4Ti5O12 (M-Na4Ti5O12) as a potential sodium-ion battery anode material. In contrast to the previously investigated trigonal phase (T-Na4Ti5O12), MNa4Ti5O12 has continuous two-dimensional (2D) channels with partially occupied Na sites, providing broader pathways and more space for the intercalation of excess sodium. Neutron powder diffraction reveals the preferred sites and occupancies of the excess sodium as well as the sodium ion conduction pathway. Electrochemical measurements show that it exhibits a comparable or higher reversible capacity than T-Na4Ti5O12. In situ synchrotron X-ray diffraction under electrochemical cycling shows that the crystal lattice undergoes strongly anisotropic volume changes during cycling.

  4. Effect of anodization and alkali-heat treatment on the bioactivity of titanium implant material (an in vitro study)

    Science.gov (United States)

    Abdelrahim, Ramy A.; Badr, Nadia A.; Baroudi, Kusai

    2016-01-01

    Objective: This study was aimed to assess the effect of anodized and alkali-heat surface treatment on the bioactivity of titanium alloy (Ti-6Al-4V) after immersion in Hank's solution for 7 days. Materials and Methods: Fifteen titanium alloy samples were used in this study. The samples were divided into three groups (five for each), five samples were anodized in 1M H3PO4 at constant voltage value of 20 v and another five samples were alkali-treated in 5 M NaOH solution for 25 min at temperature 60°C followed by heat treatment at 600°C for 1 h. All samples were then immersed in Hank's solution for 7 days to assess the effect of surface modifications on the bioactivity of titanium alloy. The different treated surfaces and control one were characterized by X-ray diffraction, atomic force microscopy, scanning electron microscopy, energy-dispersive X-ray spectroscopy, and Fourier transformation infra-red spectroscopy. Statistical analysis was performed with PASW Statistics 18.0® (Predictive Analytics Software). Results: Anodization of Ti-alloy samples (Group B) led to the formation of bioactive titanium oxide anatase phase and PO43− group on the surface. The alkali-heat treatment of titanium alloy samples (Group C) leads to the formation of bioactive titania hydrogel and supplied sodium ions. The reaction between the Ti sample and NaOH alkaline solution resulted in the formation of a layer of amorphous sodium titania on the Ti surface, and this layer can induce apatite deposition. Conclusions: The surface roughness and surface chemistry had an excellent ability to induce bioactivity of titanium alloy. The anodization in H3PO4 produced anatase titanium oxide on the surface with phosphate originated from electrolytes changed the surface topography and allowed formation of calcium-phosphate. PMID:27382532

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

    International Nuclear Information System (INIS)

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

  6. Synthesis of nano structured particles for Li-ion cathodic and anodic materials obtained by spray pyrolysis

    International Nuclear Information System (INIS)

    The development of the nano technology has contributed to improve the electrochemical properties in rechargeable batteries. The Spray Pyrolysis method allows to obtain nano structured materials with spherical morphology, narrow particle size distribution and compositional homogeneity. Nano structured particles have been prepared in this work to be used as anodic and cathodic materials in lithium-ion batteries. Among the cathodic materials, the Na-Si-Con (Li3Fe2(PO4)3) structure and the olivine (LiFePO4) phases have been synthesised. The Na-Si-Con iron phosphate favours the accommodation of the ion host, the diffusion and thermal stability. The olivine structure has an open three-dimensional network, favourable for hosting Lithium ions. The characterization by X ray diffraction, electron microscopy (scanning and transmission) and electron diffraction have allowed to identify a mix of crystalline phases of LiFePO4 (Olivine) and Li3Fe2(PO4)3 (Na-Si-Con). Thermal treatments produce porous particles. The tryphilite phase (olivine) appears after a thermal treatment at 800 degree centigrade/12h. Electrochemical results confirm the presence of the Na-Si-Con and olivine phases. Among the materials for being used as anode, the titanium oxides have been classified as good candidates as lithium ion host. The synthesis results in different experimental conditions for obtaining spherical and nano structured titanium oxide particles are presented. (Author)

  7. Electrical Conductivity and Corrosion Resistance of ZnFe2O4-Based Materials Used as Inert Anode for Aluminum Electrolysis

    Institute of Scientific and Technical Information of China (English)

    1999-01-01

    ZnFe2O4 and ZnFe2O4-based materials were tested to obtain the electrical conductivity and corrosion resistance in melting bath for aluminum electrolysis. The results proved that adequate additives, such as Ni2O3 CuO,Cu, ZnO and CeO2 would increase the electrical conductivity, and the ZnFe2O4-based anodes with these additives were of good corrosion resistance. The current density on anode, the mole ratio of NaF/AlF3 (MR) and the content of alumina in the bath effect the anode corrosion rate in different way.

  8. Lignin-based active anode materials synthesized from low-cost renewable resources

    Energy Technology Data Exchange (ETDEWEB)

    Rios, Orlando; Tenhaeff, Wyatt Evan; Daniel, Claus; Dudney, Nancy Johnston; Johs, Alexander; Nunnery, Grady Alexander; Baker, Frederick Stanley

    2016-06-07

    A method of making an anode includes the steps of providing fibers from a carbonaceous precursor, the carbon fibers having a glass transition temperature T.sub.g. In one aspect the carbonaceous precursor is lignin. The carbonaceous fibers are placed into a layered fiber mat. The fiber mat is fused by heating the fiber mat in the presence of oxygen to above the T.sub.g but no more than 20% above the T.sub.g to fuse fibers together at fiber to fiber contact points and without melting the bulk fiber mat to create a fused fiber mat through oxidative stabilization. The fused fiber mat is carbonized by heating the fused fiber mat to at least 650.degree. C. under an inert atmosphere to create a carbonized fused fiber mat. A battery anode formed from carbonaceous precursor fibers is also disclosed.

  9. Marine microbial fuel cell : use of stainless steel electrodes as anode and cathode materials

    OpenAIRE

    Dumas, Claire; Mollica, Alfonso; Féron, Damien; Basséguy, Régine; Etcheverry, Luc; Bergel, Alain

    2007-01-01

    Numerous biocorrosion studies have stated that biofilms formed in aerobic seawater induce an efficient catalysis of the oxygen reduction on stainless steels. This property was implemented here for the first time in a marine microbial fuel cell (MFC). A prototype was designed with a stainless steel anode embedded in marine sediments coupled to a stainless steel cathode in the overlying seawater. Recording current/potential curves during the progress of the experiment confirmed that the cath...

  10. Electrochemical characteristics of ternary and quadruple lithium silicon nitrides as anode material for lithium ion batteries: the influence of precursors

    Institute of Scientific and Technical Information of China (English)

    WEN Zhongsheng; TIAN Feng; SUN Juncai; JI Shijun; XIE Jingying

    2008-01-01

    Ternary and quadruple lithium silicon nitride anode materials for lithium ion batteries with different precursors were prepared by the simple process of high-energy ball milling.High capacity and excellent cyclability were obtained.The influence of precursor introduction on the electrochemical performance of products was investigated.This research reveals that the electrochemical performance of lithium silicon hiaide can be enhanced significantly by doping O.The cyclability of quadruple lithium silicon nitride can be optimized remarkably by controlling the introduction quantity of the precursors.It is possible for the composite to be used as a capacity compensator within a wide voltage cut-off window.

  11. A novel Si/Sn composite with entangled ribbon structure as anode materials for lithium ion battery

    Science.gov (United States)

    Wu, Jinbo; Zhu, Zhengwang; Zhang, Hongwei; Fu, Huameng; Li, Hong; Wang, Aimin; Zhang, Haifeng

    2016-07-01

    A novel Si/Sn composite anode material with unique ribbon structure was synthesized by Mechanical Milling (MM) and the structural transformation was studied in the present work. The microstructure characterization shows that Si/Sn composite with idealized entangled ribbon structured can be obtained by milling the mixture of the starting materials, Si and Sn for 20 h. According to the calculated results based on the XRD data, the as-milled 20 h sample has the smallest avergae crystalline size. It is supposed that the flexible ribbon structure allows for accommodation of intrinsic damage, which significantly improves the fracture toughness of the composite. The charge and discharge tests of the as-milled 20 h sample have been performed with reference to Li+/Li at a current density of 400 mA g‑1 in the voltage from 1.5 to 0.03 V (vs Li/Li+) and the result shows that the initial capacity is ∼1400 mA h g‑1, with a retention of ∼1100 mA h g‑1 reversible capacity after 50 cycles, which is possible serving as the promising anode material for the lithium ion battery application.

  12. Synthesis and Electrochemical Properties of CNFs-Si Composites as an Anode Material for Li Secondary Batteries.

    Science.gov (United States)

    Park, Eun-Sil; Park, Heai-Ku; Park, Ho-Seon; Lee, Chang-Seop

    2015-11-01

    We have performed a study on the electrochemical and structural characteristics of CNFs-Si composites which are active anode material for lithium secondary batteries. Carbon nanofibers (CNFs) have been synthesized by Chemical Vapor Deposition (CVD) using Co and Cu catalysts. The CNFs on the surface of the Si particle can provide a flexible space to relieve the volumetric expansion during a charge. Therefore, the CNFs composites on Si particles were prepared on the basis of the following two processes: (1) CNFs were grown on the simple mechanical mixture of Si particles and catalysts (CNFs/Si); (2) CNFs were grown on the surface of a pyrolytic carbon that was coated with Si particles (CNFs/PC/Si). The morphology and composition of CNFs-Si composites were analyzed by SEM and EDS measurements. Crystallinity and amorphicity were investigated using XRD and Raman spectroscopy. The characteristics of the synthesized CNFs-Si composites were analyzed through XPS, TGA, and BET. The two different CNFs-Si composite materials were evaluated as the anodic material in three different electrode cells. We found that the initial capacity of the CNFs/PC/Si composite electrode was 1,361 mAh/g with retention rate of 28.4%, which was better than the retention rate of 4.9% with the CNFs/Si electrode.

  13. Biotemplated fabrication of Sn@C anode materials based on the unique metal biosorption behavior of microalgae.

    Science.gov (United States)

    Tao, Xinyong; Wu, Rui; Xia, Yang; Huang, Hui; Chai, Weicong; Feng, Tong; Gan, Yongping; Zhang, Wenkui

    2014-03-12

    Biotemplating is an effective strategy to obtain morphology-controllable materials with structural specificity, complexity, and corresponding unique functions. Different from traditional biotemplating strategies replicating the morphology and using biogenic elements of biomaterials (e.g., C, Si, N, Fe, P, S), we take advantage of the unique heavy-metal-ion biosorption behavior of microalgae to fabricate tin-decorated carbon (Sn@C) anode materials for lithium-ion batteries. Microalgae Spirulina platensis is used as the biotemplate, the renewable carbon source, and the biosorbent. After a facile one-step heat treatment, Sn@C with tin particles (20-30 nm) dispersing into the porous carbon matrix can be obtained. Fourier transform infrared spectra reveal that metal-ion biosorption results from the complexation reactions between Sn(4+) ions and the hydroxyl groups associated with alginate. The Sn@C anode shows a discharge capacity of 520 mAh g(-1) after 100 cycles, as well as excellent cycle stability and high coulombic efficiency (approximately 100%), exhibiting fascinating electrochemical performance. This facile, green, and economical strategy not only will extend the scope of biotemplating synthesis of functional materials but also will provide reference for environmental protection and water purification. PMID:24517475

  14. A novel Si/Sn composite with entangled ribbon structure as anode materials for lithium ion battery.

    Science.gov (United States)

    Wu, Jinbo; Zhu, Zhengwang; Zhang, Hongwei; Fu, Huameng; Li, Hong; Wang, Aimin; Zhang, Haifeng

    2016-01-01

    A novel Si/Sn composite anode material with unique ribbon structure was synthesized by Mechanical Milling (MM) and the structural transformation was studied in the present work. The microstructure characterization shows that Si/Sn composite with idealized entangled ribbon structured can be obtained by milling the mixture of the starting materials, Si and Sn for 20 h. According to the calculated results based on the XRD data, the as-milled 20 h sample has the smallest avergae crystalline size. It is supposed that the flexible ribbon structure allows for accommodation of intrinsic damage, which significantly improves the fracture toughness of the composite. The charge and discharge tests of the as-milled 20 h sample have been performed with reference to Li(+)/Li at a current density of 400 mA g(-1) in the voltage from 1.5 to 0.03 V (vs Li/Li(+)) and the result shows that the initial capacity is ∼1400 mA h g(-1), with a retention of ∼1100 mA h g(-1) reversible capacity after 50 cycles, which is possible serving as the promising anode material for the lithium ion battery application. PMID:27390015

  15. Ce-doped α-FeOOH nanorods as high-performance anode material for energy storage

    Science.gov (United States)

    Zhai, Yanjun; Xu, Liqiang; Qian, Yitai

    2016-09-01

    Ce-doped α-FeOOH nanorods with high yields were conveniently prepared by a hydrothermal method followed by an acid-treatment process. It is found that Ce uniformly distributes in the α-FeOOH nanorod nanostructures through elemental mapping analysis. The 0.5 wt% Ce-doped α-FeOOH electrode displayed excellent cycling performance with a high discharge capacity of 830 mA h g-1 after 800 charge/discharge cycles at a high current of 2000 mA g-1. The enhanced electrochemical performance can be attributed to the improved electronic conductivity, Li-ion diffusion kinetics and structure stability after Ce doping. Furthermore, a 0.5 wt% Ce-doped α-FeOOH//LiFePO4 lithium ion cell with an initial discharge capacity of 580 mA h g-1 at 1000 mA g-1 based on the total weight of the anode material has been fabricated for the first time. The obtained 0.5 wt% Ce-doped α-FeOOH electrode as anode material for sodium-ion batteries also exhibits a high initial discharge capacity of 587 mA h g-1 at 100 mA g-1.

  16. Ultrahigh capacity anode material for lithium ion battery based on rod gold nanoparticles decorated reduced graphene oxide

    Energy Technology Data Exchange (ETDEWEB)

    Atar, Necip, E-mail: necipatar@gmail.com [Department of Chemical Engineering, Pamukkale University, Denizli (Turkey); Eren, Tanju [Department of Chemical Engineering, Pamukkale University, Denizli (Turkey); Yola, Mehmet Lütfi [Department of Metallurgical and Materials Engineering, Sinop University, Sinop (Turkey)

    2015-09-01

    In this study, we report the synthesis of rod shaped gold nanoparticles/2-aminoethanethiol functionalized reduced graphene oxide composite (rdAuNPs/AETrGO) and its application as an anode material for lithium-ion batteries. The structure of the rdAuNPs/AETrGO composite was characterized by scanning electron microscopy, transmission electron microscopy, X-ray photoelectron spectroscopy and X-ray diffraction. The electrochemical performance was investigated at different current rates by using a coin-type cell. It was found that the rod shaped gold nanoparticles were highly dispersed on the reduced graphene oxide sheets. Moreover, the rdAuNPs/AETrGO composite showed a high specific gravimetric capacity of about 1320 mAh g{sup −1} and a long-term cycle stability. - Highlights: • We prepared rod shaped gold nanoparticles functionalized reduced graphene oxide. • The nanocomposite was used as an anode material for lithium-ion batteries. • The nanocomposite showed a high specific gravimetric capacity of about 1320 mAh g{sup −1}. • The nanocomposite exhibited a long-term cycle stability.

  17. Ultrahigh capacity anode material for lithium ion battery based on rod gold nanoparticles decorated reduced graphene oxide

    International Nuclear Information System (INIS)

    In this study, we report the synthesis of rod shaped gold nanoparticles/2-aminoethanethiol functionalized reduced graphene oxide composite (rdAuNPs/AETrGO) and its application as an anode material for lithium-ion batteries. The structure of the rdAuNPs/AETrGO composite was characterized by scanning electron microscopy, transmission electron microscopy, X-ray photoelectron spectroscopy and X-ray diffraction. The electrochemical performance was investigated at different current rates by using a coin-type cell. It was found that the rod shaped gold nanoparticles were highly dispersed on the reduced graphene oxide sheets. Moreover, the rdAuNPs/AETrGO composite showed a high specific gravimetric capacity of about 1320 mAh g−1 and a long-term cycle stability. - Highlights: • We prepared rod shaped gold nanoparticles functionalized reduced graphene oxide. • The nanocomposite was used as an anode material for lithium-ion batteries. • The nanocomposite showed a high specific gravimetric capacity of about 1320 mAh g−1. • The nanocomposite exhibited a long-term cycle stability

  18. Yolk-shell ZnO-C microspheres with enhanced electrochemical performance as anode material for lithium ion batteries

    International Nuclear Information System (INIS)

    Graphical abstract: - Highlights: • ZnO-C yolk-shell microspheres, hollow microspheres and solid microspheres are prepared. • Yolk-shell ZnO-C microspheres possess the best electrochemical properties when used as the anode materials for lithium-ion batteries. • The special yolk-shell structures and extra carbon support account for the enhanced electrochemical properties. - Abstract: Three ZnO-C samples with distinct structures including yolk-shell microspheres, hollow microspheres and solid microspheres are fabricated through a facile chemical solution reaction followed by calcination in argon. When employed as the anode materials for lithium ion batteries, yolk-shell ZnO-C microspheres exhibit the best electrochemical properties than the hollow and solid microspheres. After 150 cycles, yolk-shell ZnO-C microspheres demonstrate a relative high capacity of 520 mA h g−1 at a current density of 100 mA g−1 with a Coulombic efficiency of about 99.3%. The excellent cycling stability and good rate capability of yolk-shell ZnO-C microspheres stem from the synergistic effect of the unique yolk-shell structures and extra carbon support

  19. Synthesis And Electrochemical Characteristics Of Mechanically Alloyed Anode Materials SnS2 For Li/SnS2 Cells

    Directory of Open Access Journals (Sweden)

    Hong J.H.

    2015-06-01

    Full Text Available With the increasing demand for efficient and economic energy storage, tin disulfide (SnS2, as one of the most attractive anode candidates for the next generation high-energy rechargeable Li-ion battery, have been paid more and more attention because of its high theoretical energy density and cost effectiveness. In this study, a new, simple and effective process, mechanical alloying (MA, has been developed for preparing fine anode material tin disulfides, in which ammonium chloride (AC, referred to as process control agents (PCAs, were used to prevent excessive cold-welding and accelerate the synthesis rates to some extent. Meanwhile, in order to decrease the mean size of SnS2 powder particles and improve the contact areas between the active materials, wet milling process was also conducted with normal hexane (NH as a solvent PCA. The prepared powders were both characterized by X-ray diffraction, Field emission-scanning electron microscopeand particle size analyzer. Finally, electrochemical measurements for Li/SnS2 cells were takenat room temperature, using a two-electrode cell assembled in an argon-filled glove box and the electrolyte of 1M LiPF6 in a mixture of ethylene carbonate(EC/dimethylcarbonate (DMC/ethylene methyl carbonate (EMC (volume ratio of 1:1:1.

  20. Trace analysis of Cd, Cu, Pb and Zn in various materials using differential pulse anodic stripping voltammetry

    International Nuclear Information System (INIS)

    Sampling and sample preparation methods have been described. Digestion methods for different types of materials and acid purification systems have been developed. For trace analysis purposes cleaning methods for glassware etc. have been described. Differential pulse anodic stripping voltametric (DPASV) method has been worked out for the trace analysis of zn, cd, pb and Cu in different types of materials. Linearity of the method has been checked by drawing concentration versus currents (peak height) curves. Precision of the method has been checked by analysing a number of actual samples. of the method has been verified by analysing standards of U.S.A. Comparative studies have been done between Differential pulse anodic stripping voltammetric method and Atomic Absorption spectroscopic method. Problems of contamination and systematic errors during trace and ultra-trace analysis have been discussed. A variety of samples including soil, spinach, wheat flour, rice flour, dry milk, coriander, kidney stones, bladder stones etc. have been analysed and preliminary results have been reported. (author)

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

    Energy Technology Data Exchange (ETDEWEB)

    Stephen Everett Treimer

    2002-06-27

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

  2. Cellulose-based carbon-A potential anode material for lithium-ion battery

    Science.gov (United States)

    Kierzek, Krzysztof; Piotrowska, Aleksandra; Machnikowski, Jacek

    2015-11-01

    A series of hard carbons was produced by the carbonization of microcrystalline cellulose powder in the temperature range of 950-1100 °C. The properties of the carbons were characterized using elemental analysis, X-ray diffraction and N2 and CO2 adsorption. The effect of heat-treatment temperature (HTT), pyrolytic carbon (PC) coating and discharging mode on the lithium insertion/deinsertion behavior of the carbons was assessed in a coin-type half-cell with metal lithium cathode. Increasing cellulose HTT modifies mostly carbon porosity, the surface area (SDFT) decreases from about 500 to 167 m2 g-1. It is associated with lowering the reversible Crev and irreversible Cirr capacities, but without improving relatively low (0.72) 1st cycle coulombic efficiency. Applying constant current (CC)+constant voltage (CV) discharging mode instead of conventional CC enhances the reversible capacity by 15-18%. PC coating is effective in reducing Cirr by ∼20% with a little change of Crev. The best capacity parameters, Crev of 458 mA h g-1 and Cirr of 139 mA h g-1, were measured for PC coated 1000 °C carbon. The prolonged cycling of full-cell assembled with anode of the carbon and commercial cathode revealed that after initial 20 cycles the capacity decay (0.029 mA h/cycle) is comparable to that of commercial cell with graphite-based anode.

  3. Electrospun fibers for high performance anodes in microbial fuel cells. Optimizing materials and architecture

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Shuiliang

    2010-04-15

    A novel porous conducting nanofiber mat (PCNM) with nanostructured polyaniline (nanoPANi) on the fiber surface was successfully prepared by simple oxidative polymerization. The composite PCNM displayed a core/shell structure with highly rough surface. The thickness and the morphology of PANi layer on the electrospun polyamide (PA) fiber surface could be controlled by varying aniline concentration and temperature. The combination of the advantages of electrospinning technique and nanostructured PANi, let the PA/PANi composite PCNM possess more than five good properties, i.e. high conductivity of 6.759 S.m{sup -1}, high specific surface area of 160 m2.g{sup -1}, good strength of 82.88 MPa for mat and 161.75 MPa for highly aligned belts, good thermal properties with 5% weight loss temperature up to 415 C and excellent biocompatibility. In the PA/PANi composite PCNM, PANi is the only conducting component, its conductivity of 6.759 S.m{sup -1} which is measured in dry-state, is not enough for electrode. Moreover, the conductivity decreases in neutral pH environment due to the de-doping of proton. However, the method of spontaneous growth of nanostructured PANi on electrospun fiber mats provides an effective method to produce porous electrically conducting electrospun fiber mats. The combination advantages of nanostructured PANi with the electrospun fiber mats, extends the applications of PANi and electrospun nanofibers, such as chemical- and bio-sensors, actuators, catalysis, electromagnetic shielding, corrosion protection, separation membranes, electro-optic devices, electrochromic devices, tissue engineering and many others. The electrical conductivity of electrospun PCNM with PANi as the only conducting component is too low for application of as anode in microbial fuel cells (MFCs). So, we turn to electrospun carbon fiber due to its high electrical conductivity and environmental stability. The current density is greatly dependent on the microorganism density of anode

  4. Electrospinning synthesis of 3D porous NiO nanorods as anode material for lithium-ion batteries

    Directory of Open Access Journals (Sweden)

    Wei Kong Xiang

    2016-06-01

    Full Text Available Three-dimensional NiO nanorods were synthesized as anode material by electrospinning method. X-ray diffraction results revealed that the product sintered at 400 °C had impure metallic nickel phase which, however, became pure NiO phase as the sintering temperature rose. Nevertheless, the nanorods sintered at 400, 500 and 600 °C had similar diameters (∼200 nm.The NiO nanorod material sintered at 500 °C was chip-shaped with a diameter of 200 nm and it exhibited a porous 3D structure. The nanorod sintered at 500 °C had the optimal electrochemical performance. Its discharge specific capacity was 1127 mAh·g−1 initially and remained as high as 400 mAh·g−1 at a current density of 55 mA·g−1 after 50 cycles.

  5. Zinc pyridinedicarboxylate micro-nanostructures: Promising anode materials for lithium-ion batteries with excellent cycling performance.

    Science.gov (United States)

    Fei, Hailong; Lin, Yaqin

    2016-11-01

    It is important to discover new, cheap and environmental friendly coordination polymer electrode materials for lithium-ion batteries. Zinc 2,6-pyridilinedicarboxylate particles show better cycling stability and higher discharge capacity than 2,5-pyridilinedicarboxylate micro-platelets when they are firstly tested as anode materials for lithium-ion batteries. The former can steadily cycle at current densities of 750, 1000 and 2000mAg(-1). It is also stable in multiple insertion/extraction processes at current densities of 750, 1500, 2000, 2500, 3000, and 750mAg(-1), and the capacity retention is 77.9% after 60cycles. While the latter is apt to show good cycling performance at smaller discharge current density. PMID:27490195

  6. Development of Low Cost Carbonaceous Materials for Anodes in Lithium-Ion Batteries for Electric and Hybrid Electric Vehicles

    Energy Technology Data Exchange (ETDEWEB)

    Barsukov, Igor V.

    2002-12-10

    Final report on the US DOE CARAT program describes innovative R & D conducted by Superior Graphite Co., Chicago, IL, USA in cooperation with researchers from the Illinois Institute of Technology, and defines the proper type of carbon and a cost effective method for its production, as well as establishes a US based manufacturer for the application of anodes of the Lithium-Ion, Lithium polymer batteries of the Hybrid Electric and Pure Electric Vehicles. The three materials each representing a separate class of graphitic carbon, have been developed and released for field trials. They include natural purified flake graphite, purified vein graphite and a graphitized synthetic carbon. Screening of the available on the market materials, which will help fully utilize the graphite, has been carried out.

  7. Research progress in anode materials for Li-ion battery%锂离子电池负极材料的研究进展

    Institute of Scientific and Technical Information of China (English)

    武明昊; 陈剑; 王崇; 衣宝廉

    2011-01-01

    综述了近年来锂离子电池负极材料的研究进展,包括碳材料、过渡金属氧化物,锡基和硅基材料等,重点评述了锡基和硅基材料的研究进展,并对锂离子电池负极材料的发展趋势进行了展望.%Research progress in anode materials for Li-ion battery in recent years, including carbon, transition metal oxides, tin based composites and silicon based composites was reviewed. The research progress in tin based and silicon based anode materials was commented emphatically,the development tendency of Li-ion battery anode materials was prospected.

  8. 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.

  9. Corrosion and Discharge Behaviors of Mg-Al-Zn and Mg-Al-Zn-In Alloys as Anode Materials

    Directory of Open Access Journals (Sweden)

    Jiarun Li

    2016-03-01

    Full Text Available The Mg-6%Al-3%Zn and Mg-6%Al-3%Zn-(1%, 1.5%, 2%In alloys were prepared by melting and casting. Their microstructures were investigated via metallographic and energy-dispersive X-ray spectroscopy (EDS analysis. Moreover, hydrogen evolution and electrochemical tests were carried out in 3.5 wt% NaCl solution aiming at identifying their corrosion mechanisms and discharge behaviors. The results suggested that indium exerts an improvement on both the corrosion rate and the discharge activity of Mg-Al-Zn alloy via the effects of grain refining, β-Mg17Al12 precipitation, dissolving-reprecipitation, and self-peeling. The Mg-6%Al-3%Zn-1.5%In alloy with the highest corrosion rate at free corrosion potential did not perform desirable discharge activity indicating that the barrier effect caused by the β-Mg17Al12 phase would have been enhanced under the conditions of anodic polarization. The Mg-6%Al-3%Zn-1.0%In alloy with a relative low corrosion rate and a high discharge activity is a promising anode material for both cathodic protection and chemical power source applications.

  10. Micro-nanostructured CuO/C spheres as high-performance anode materials for Na-ion batteries.

    Science.gov (United States)

    Lu, Yanying; Zhang, Ning; Zhao, Qing; Liang, Jing; Chen, Jun

    2015-02-14

    In this paper, we report on the synthesis of micro-nanostructured CuO/C spheres by aerosol spray pyrolysis and their application as high-performance anodes in sodium-ion batteries. Micro-nanostructured CuO/C spheres with different CuO contents were synthesized through aerosol spray pyrolysis by adjusting the ratio of reactants and heat-treated by an oxidation process. The as-prepared CuO/C spheres show uniformly spherical morphology, in which CuO nanoparticles (∼10 nm) are homogeneously embedded in the carbon matrix (denoted as 10-CuO/C). The electrochemical performance of 10-CuO/C with a carbon weight of 44% was evaluated as the anode material for Na-ion batteries. It can deliver a capacity of 402 mA h g(-1) after 600 cycles at a current density of 200 mA g(-1). Furthermore, a capacity of 304 mA h g(-1) was obtained at a high current density of 2000 mA g(-1). The superior electrochemical performance of the micro-nanostructured CuO/C spheres leads to the enhancement of the electronic conductivity of the nanocomposite and the accommodation of the volume variation of CuO/C during charge/discharge cycling. PMID:25584745

  11. Effect of tar fractions from coal gasification on nickel-yttria stabilized zirconia and nickel-gadolinium doped ceria solid oxide fuel cell anode materials

    Science.gov (United States)

    Lorente, E.; Berrueco, C.; Millan, M.; Brandon, N. P.

    2013-11-01

    The allowable tar content in gasification syngas is one of the key questions for the exploitation of the full potential of fuel cell concepts with integrated gasification systems. A better understanding of the interaction between tars and the SOFC anodes which leads to carbon formation and deposition is needed in order to design systems where the extent of gas cleaning operations is minimized. Model tar compounds (toluene, benzene, naphthalene) have been used in experimental studies to represent those arising from biomass/coal gasification. However, the use of toluene as a model tar overestimates the negative impact of a real gasification tar on SOFC anode degradation associated with carbon formation. In the present work, the effect of a gasification tar and its distillation fractions on two commercially available fuel cell anodes, Ni/YSZ (yttria stabilized zirconia) and Ni/CGO (gadolinium doped ceria), is reported. A higher impact of the lighter tar fractions was observed, in terms of more carbon formation on the anodes, in comparison with the whole tar sample. The characterization of the recovered tars after contact with the anode materials revealed a shift towards a heavier molecular weight distribution, reinforcing the view that these fractions have reacted on the anode.

  12. Mesoporous Carbon-Tin Nanocomposites as Anode Materials for Li-ion Battery

    Institute of Scientific and Technical Information of China (English)

    Z.W.Zhao; Z.P.Guo; P.Yao; H.K.Liu

    2008-01-01

    A new mesoporous carbon-tin (MC-Sn) nanocomposite has been successfully prepared via a two-step method. From the transmission electron microscopy (TEM) observations, the tin nanoparticles were decorated on the as-prepared mesoporous carbons. The mesoprous structure of the carbon can effectively buffer the volume changes during the Li-Sn alloying and de-alloying cycles. The as-prepared MC/Sn nanocomposite electrodes exhibited extremely good cycling stability, with the specific capacity of Sn in the composite electrode calculated to be 959.7 mAh-g-1, which amounts to an impressive 96.9% of the theoretical value (990 mAh·g-1). The reversible capacity after 200 cycles is 96.1% of the first cycle reversible capacity, i.e., the capacity fade rate is only 0.0195% per cycle, which is even better than that of commercial graphite-based anodes.

  13. Nanoparticle Decorated Ultrathin Porous Nanosheets as Hierarchical Co3O4 Nanostructures for Lithium Ion Battery Anode Materials

    DEFF Research Database (Denmark)

    Mujtaba, Jawayria; Sun, Hongyu; Huang, Guoyong;

    2016-01-01

    We report a facile synthesis of a novel cobalt oxide (Co3O4) hierarchical nanostructure, in which crystalline core-amorphous shell Co3O4 nanoparticles with a bimodal size distribution are uniformly dispersed on ultrathin Co3O4 nanosheets. When tested as anode materials for lithium ion batteries......, the as-prepared Co3O4 hierarchical electrodes delivered high lithium storage properties comparing to the other Co3O4 nanostructures, including a high reversible capacity of 1053.1 mAhg-1 after 50 cycles at a current density of 0.2 C (1 C = 890 mAg-1), good cycling stability and rate capability....

  14. Interconnected MoO2 nanocrystals with carbon nanocoating as high-capacity anode materials for lithium-ion batteries.

    Science.gov (United States)

    Zhou, Liang; Wu, Hao Bin; Wang, Zhiyu; Lou, Xiong Wen David

    2011-12-01

    A facile one-pot hydrothermal method has been developed for the preparation of carbon-coated MoO(2) nanocrystals. The annealed MoO(2)-C nanocomposite consists of interconnected MoO(2)@C nanocrystals. When evaluated for lithium storage capabilities, these MoO(2)@C nanocrystals exhibit high specific capacities (~640 mA h g(-1) at 200 mA g(-1) and ~575 mA h g(-1) at 400 mA g(-1)) and excellent cycling stability. In view of the excellent lithium storage properties and the ease in large-scale preparation, the as-synthesized MoO(2)-C nanocomposite might be used as promising anode materials for high-performance lithium-ion batteries. PMID:22077330

  15. A novel ZnO@Ag@Polypyrrole hybrid composite evaluated as anode material for zinc-based secondary cell

    Science.gov (United States)

    Huang, Jianhang; Yang, Zhanhong; Feng, Zhaobin; Xie, Xiaoe; Wen, Xing

    2016-04-01

    A novel ZnO@Ag@Polypyrrole nano-hybrid composite has been synthesized with a one-step approach, in which silver-ammonia complex ion serves as oxidant to polymerize the pyrrole monomer. X-ray diffraction (XRD) and infrared spectroscopy (IR) show the existence of metallic silver and polypyrrole. The structure of nano-hybrid composites are characterized by scanning electron microscope (SEM) and transmission electron microscope (TEM), which demonstrates that the surface of ZnO is decorated with nano silver grain coated with polypyrrole. When evaluated as anode material, the silver grain and polypyrrole layer not only suppress the dissolution of discharge product, but also helps to uniform electrodeposition due to substrate effect and its good conductivity, thus shows better cycling performance than bare ZnO electrode does.

  16. Effect of carbon coating on electrochemical performance of hard carbons as anode materials for lithium-ion batteries

    Science.gov (United States)

    Lee, Jong-Hyuk; Lee, Heon-Young; Oh, Seh-Min; Lee, Seo-Jae; Lee, Ki-Young; Lee, Sung-Man

    Surface modification by a soft-carbon coating is used to improve the electrochemical performance of hard carbons as the negative-electrode (anode) material in lithium-ion batteries. The coating process involves simple heat-treatment of a mixture of coal-tar pitch and hard carbon powders at 1000 °C. The carbon coating significantly reduces the reaction of lithium with surface functional groups or absorbed species caused by air exposure. This is attributed to the effective suppression of the diffusion of both air and water into the hard carbon by the soft-carbon coating, and the better resistance of soft carbon to air. As a result, the charge-discharge coulombic efficiency during cycling, as well as during the first cycle, is improved.

  17. Carbon-coated Ni 20Si 80 alloy-graphite composite as an anode material for lithium-ion batteries

    Science.gov (United States)

    Lee, Heon-Yong; Kim, Young-Lae; Hong, Moon-Ki; Lee, Sung-Man

    A carbon-coated Ni 20Si 80 alloy-graphite composite has been studied as the anode for lithium-ion batteries. The composite is prepared by simple heat-treatment of a mixture of coal tar pitch and a Ni 20Si 80-graphite composite at 900 °C and under argon. The Ni 20Si 80 alloy powders are synthesized by mechanical alloying. The composite demonstrates promising electrochemical properties such as high reversible capacity, excellent cycle performance, and sufficiently high initial charge-discharge coulombic efficiency. This suggests buffering and conductive actions on the main active material, viz., Ni 20Si 80 alloy, of the graphite. These two effects are strongly enhanced by the carbon coating treatment.

  18. Synthesis of Hierarchical CoO Nano/Microstructures as Anode Materials for Lithium-Ion Batteries

    Directory of Open Access Journals (Sweden)

    Dan Qin

    2014-01-01

    Full Text Available Hierarchical CoO nano/microstructures are synthesized via a hydrothermal method and a subsequent annealed process. When evaluated for use in lithium-ion batteries, hierarchical CoO nano/microstructures show a high initial discharge capacity of 1370 mAh/g and a high reversible capacity of 1148 mAh/g over 20 cycles at a current density of 100 mA/g. Superior rate performance with coulombic efficiency of about 100% upon galvanostatic cycling is also revealed. The excellent electrochemical properties of hierarchical CoO nano/microstructures make it a promising alternative anode material for high power lithium-ion batteries applications.

  19. Nb{sub 2}O{sub 5} hollow nanospheres as anode material for enhanced performance in lithium ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Sasidharan, Manickam [Department of Chemistry, Faculty of Science and Engineering, Saga University, 1 Honjo-machi, Saga 840-8502 (Japan); Gunawardhana, Nanda [Advanced Research Center, Saga University, 1341 Yoga-machi, Saga 840-0047 (Japan); Yoshio, Masaki, E-mail: yoshio@cc.saga-u.ac.jp [Advanced Research Center, Saga University, 1341 Yoga-machi, Saga 840-0047 (Japan); Nakashima, Kenichi, E-mail: nakashik@cc.saga-u.ac.jp [Department of Chemistry, Faculty of Science and Engineering, Saga University, 1 Honjo-machi, Saga 840-8502 (Japan)

    2012-09-15

    Graphical abstract: Nb{sub 2}O{sub 5} hollow nanosphere constructed electrode delivers high capacity of 172 mAh g{sup −1} after 250 cycles and maintains structural integrity and excellent cycling stability. Highlights: ► Nb{sub 2}O{sub 5} hollow nanospheres synthesis was synthesized by soft-template. ► Nb{sub 2}O{sub 5} hollow nanospheres were investigated as anode material in Li-ion battery. ► Nanostructured electrode delivers high capacity of 172 mAh g{sup −1} after 250 cycles. ► The electrode maintains the structural integrity and excellent cycling stability. ► Nanosized shell domain facilitates fast lithium intercalation/deintercalation. -- Abstract: Nb{sub 2}O{sub 5} hollow nanospheres of average diameter ca. ∼29 nm and hollow cavity size ca. 17 nm were synthesized using polymeric micelles with core–shell–corona architecture under mild conditions. The hollow particles were thoroughly characterized by transmission electron microscope (TEM), X-ray diffraction (XRD), infrared spectroscopy (FTIR), thermal (TG/DTA) and nitrogen adsorption analyses. Thus obtained Nb{sub 2}O{sub 5} hollow nanospheres were investigated as anode materials for lithium ion rechargeable batteries for the first time. The nanostructured electrode delivers high capacity of 172 mAh g{sup −1} after 250 cycles of charge/discharge at a rate of 0.5 C. More importantly, the hollow particles based electrodes maintains the structural integrity and excellent cycling stability even after exposing to high current density 6.25 A g{sup −1}. The enhanced electrochemical behavior is ascribed to hollow cavity coupled with nanosized Nb{sub 2}O{sub 5} shell domain that facilitates fast lithium intercalation/deintercalation kinetics.

  20. FeS/C composite as high-performance anode material for alkaline nickel-iron rechargeable batteries

    Science.gov (United States)

    Shangguan, Enbo; Li, Fei; Li, Jing; Chang, Zhaorong; Li, Quanmin; Yuan, Xiao-Zi; Wang, Haijiang

    2015-09-01

    FeS and its composite, FeS/C, are synthesized via a simple calcination method followed by a co-precipitation process. The electrochemical properties of the bare FeS and FeS/C composite as anode materials for alkaline nickel-iron batteries are investigated. The results show that the FeS/C-3wt%Bi2O3-mixed electrode delivers a high specific capacity of 325 mAh g-1 at a current density of 300 mA g-1 with a faradaic efficiency of 90.3% and retains 99.2% of the initial capacity after 200 cycles. For the first time, it is demonstrated that even at a discharge rate as high as 1500 mA g-1 (5C) the FeS/C-3wt%Bi2O3-mixed electrode delivers a specific capacity of nearly 230 mAh g-1. SEM results confirm that after 200 discharge-charge cycles, the size of FeS/C particles reduces from 5 to 15 μm to less than 300 nm in diameter and the particles are highly dispersed on the surface of carbon black, which is likely caused by the dissolution-deposition process of Fe(OH)2 and Fe via intermediate iron species. As a result, the FeS/C composite exhibits considerably high charge efficiency, high discharge capacities, excellent rate capability and superior cycling stability. We believe that this composite is a potential candidate of high-performance anode materials for alkaline iron-based rechargeable batteries.

  1. A Co(OH){sub 2}-graphene nanosheets composite as a high performance anode material for rechargeable lithium batteries

    Energy Technology Data Exchange (ETDEWEB)

    He, Y.S.; Yang, X.; Liao, X.Z.; Ma, Z.F. [Shanghai Jiao Tong Univ. (China). Dept. of Chemical Engineering; Chen, J. [Wollongong Univ., NSW (Australia). ARC Centre of Excellence for Electromaterials Science, Intelligent Polymer Research Inst.

    2010-07-01

    The 2-D structure of graphene provides it with excellent electronic conductivity, and a high surface area. Graphene nanosheets have been investigated for use in lithium-ion (Li-ion) storage applications. In this study nanostructured TiO{sub 2}-graphene hybrid materials were fabricated in order to investigate their potential uses in Li-ion batteries. The study showed that the materials showed significantly enhanced Li-ion insertion and extraction capabilities in TiO{sub 2}. A cobalt oxide (Co(OH){sub 2})-graphene nanosheet was also developed as an advanced anode material for Li-storage. The discharge-charge cycling performance of the material was discussed, as well as the coulombic efficiency of the synthesized samples. Results of the experimental study showed that after 30 cycles, the reversible capacity of the composite achieved approximately 82 per cent of its initial value. The corresponding capacity retentions of the graphene nanosheets and the Co(OH)2 after 30 cycles were approximately 66 per cent and 58 per cent, respectively. 5 refs.

  2. Anodes for alkaline electrolysis

    Science.gov (United States)

    Soloveichik, Grigorii Lev

    2011-02-01

    A method of making an anode for alkaline electrolysis cells includes adsorption of precursor material on a carbonaceous material, conversion of the precursor material to hydroxide form and conversion of precursor material from hydroxide form to oxy-hydroxide form within the alkaline electrolysis cell.

  3. Facile complex-coprecipitation synthesis of mesoporous Fe3O4 nanocages and their high lithium storage capacity as anode material for lithium-ion batteries

    International Nuclear Information System (INIS)

    A facile complex-coprecipitation synthesis of mesoporous Fe3O4 nanocages and their high capacities and excellent cycling performance as anode material for LIBs are reported. - Highlights: • MFONs are synthesized by a facile complex-coprecipitation method. • MFONs with high surface area lead to excellent electrochemical performance. • MFONs anode retains a capacity of 573 mAh g−1 at 1 A g−1 after 300 cycles. - Abstract: In this study, high-quality mesoporous Fe3O4 nanocages (MFONs) have been synthesized by a facile complex-coprecipitation method at 100 °C with addition of triethanolamine and ethylene glycol. The as-prepared Fe3O4 nanocages possess a mesoporous structure and highly uniform dispersion. When used as an anode material for rechargeable lithium-ion batteries, MFONs anode shows high specific capacities and excellent cycling performance at high and low current rates. At a current density of 200 mA g−1, the discharge specific capacities are 876 mAh g−1 at the 2nd cycle and 830 mAh g−1 at the 100th cycle. Even at the high current density of 1000 mA g−1, MFONs anode still retains a stable capacity of 573 mAh g−1 after 300 cycles. This superior electrochemical performance is attributed to the unique mesoporous cage-like structure and high specific surface area (133 m2 g−1) of MFONs, which may offer large electrode/electrolyte contact area for the electron conduction and Li+ storage. Furthermore, the good mechanical flexibility of the mesoporous nanocages can readily buffer the massive volume expansion/shrinkage associated with the reversible electrode reaction. These results indicate that MFONs can be used as a promising high-performance anode material for lithium-ion batteries

  4. Ionic liquid-assisted solvothermal synthesis of hollow Mn2O3 anode and LiMn2O4 cathode materials for Li-ion batteries

    Science.gov (United States)

    He, Xin; Wang, Jun; Jia, Haiping; Kloepsch, Richard; Liu, Haidong; Beltrop, Kolja; Li, Jie

    2015-10-01

    Mn-based Mn2O3 anode and LiMn2O4 cathode materials are prepared by a solvothermal method combined with post annealing process. Environmentally friendly ionic liquid 1-Butyl-3-methylimidazolium tetrafluoroborate as both structure-directing agent and fluorine source is used to prepare hollow polyhedron MnF2 precursor. Both target materials Mn2O3 anode and LiMn2O4 cathode have the morphology of the MnF2 precursor. The Mn2O3 anode using carboxymethyl cellulose as binder could deliver slight better electrochemical performance than the one using poly (vinyldifluoride) as binder. The former has an initial charge capacity of 800 mAh g-1 at a current density of 101.8 mA g-1, and exhibits no obvious capacity decay for 150 cycles at 101.8 mA g-1. The LiMn2O4 cathode material prepared with molten salt assistant could display much better electrochemical performance than the one prepared without molten salt assistance. In particular, it has an initial discharge capacity of 117.5 mAh g-1 at a current density of 0.5C and good rate capability. In the field of lithium ion batteries, both the Mn2O3 anode and LiMn2O4 cathode materials could exhibit enhanced electrochemical performance due to the well formed morphology based on the ionic liquid-assisted solvothermal method.

  5. Interconnected sandwich structure carbon/Si-SiO2/carbon nanospheres composite as high performance anode material for lithium-ion batteries

    Institute of Scientific and Technical Information of China (English)

    Yuanjin Du; Mengyan Hou; Dandan Zhou; Yonggang Wang; Congxiao Wang; Yongyao Xia

    2014-01-01

    In the present work, an interconnected sandwich carbon/Si-SiO2/carbon nanospheres composite was prepared by template method and carbon thermal vapor deposition (TVD). The carbon conductive layer can not only efficiently improve the electronic conductivity of Si-based anode, but also play a key role in alleviating the negative effect from huge volume expansion over discharge/charge of Si-based anode. The resulting material delivered a reversible capacity of 1094 mAh/g, and exhibited excellent cycling stability. It kept a reversible capacity of 1050 mAh/g over 200 cycles with a capacity retention of 96%.

  6. 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.

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

    International Nuclear Information System (INIS)

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

  8. 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.

  9. Synthesis of Octahedral-Shaped NiO and Approaches to an Anode Material of Manufactured Solid Oxide Fuel Cells Using the Decalcomania Method

    Directory of Open Access Journals (Sweden)

    Haeran Cho

    2013-01-01

    Full Text Available Micrometer-sized and octahedral-shaped NiO particles were synthesized by microwave thermal treatment at 300 watt power for 15 min in a microwave chamber to be used as an anode material in solid oxide fuel cells. SEM image and particle size distribution revealed near-perfect octahedral NiO microparticle with sizes ranging from 4.0~11.0 μm. The anode functional layer (AFL, 60 wt% NiO synthesized: commercial 40 wt% YSZ, electrolyte (commercial Yttria-stabilized zirconia, YSZ, and cathode (commercial La0.8Sr0.2MnO3, LSM layers were manufactured using the decalcomania method on a porous anode support, sequentially. The sintered electrolyte at 1450°C for 2 h using the decalcomania method was dense and had a thickness of about 10 μm. The cathode was sintered at 1250°C for 2 h, and it was porous. Using humidified hydrogen as a fuel, a coin cell with a 15 μm thick anode functional layer exhibited maximum power densities of 0.28, 0.38, and 0.65 W/cm2 at 700, 750, and 800°C, respectively. Otherwise, when a commercial YSZ anode functional layer was used, the maximum power density was 0.55 W/cm2 at 800°C.

  10. Preparation and prop erties of Ce0.8Ca0.2O1.8 anode material by glycine-nitrate process

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    Ce0.8Ca0.2O1.8 (CDC82) anode material was prepared by glycine-nitrate process(GNP). Thermogravimetric(TG) analysis and differential scanning calorimetric(DSC) methods were adopted to characterize the reaction process of CDC82 material. X-ray diffractometry(XRD), scanning electron microcopy(SEM), direct current four probe (four-probe DC) and temperature process reduce(TPR) techniques were adopted to characterize the properties of CDC82 material. After the precursor was sintered at 750 ℃for 4 h, CDC82 material with pure-fluorite structure and nanometer size was obtained. The total conductivity of CDC82 changes little with temperature in air at 50-850 ℃, and the maximum value is 0.04 S/cm at 750 ℃. The total conductivity wholly becomes larger when the atmosphere changes from air to hydrogen, which greatly increases with increasing temperature and reaches the maximum value of 1.09 S/cm at 850 ℃. Some impurities such as CeMg and La2O3 exist after the mixture of CDC82 anode and La1-xSrxGa1-yMgyO3-δ (LSGM) electrolyte material is sintered at 1 200 ℃ for 15 h. The CDC82 material as anode material has excellent catalytic property for hydrogen and methane.

  11. 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.

  12. High capacity disordered carbons obtained from coconut shells as anode materials for lithium batteries

    International Nuclear Information System (INIS)

    Carbonaceous materials have been obtained by the pyrolysis of coconut shells at 800 and 900 deg. C with pore forming substances such as KOH and ZnCl2. The prepared carbons were subjected to XRD, SEM, BET-surface area and charge-discharge studies. The structure and morphology were greatly changed by porogens, which in turn influence the electrochemical properties of the carbonaceous materials. Nanocrystalline tin (Sn) particles were prepared by chemical reduction method. The cycling tests showed that the addition of nanotin with the active material offers a stable cycling behavior. The electrochemical impedance spectra for the Li/C cells have been made and the results are discussed

  13. Electrochemical Properties of Chemically Processed SiOx as Coating Material in Lithium-Ion Batteries with Si Anode

    Directory of Open Access Journals (Sweden)

    Hee-June Jeong

    2014-01-01

    Full Text Available A SiOx coating material for Si anode in lithium-ion battery was processed by using SiCl4 and ethylene glycol. The produced SiOx particles after heat treatment at 725°C for 1 h were porous and irregularly shaped with amorphous structure. Pitch carbon added to SiOx was found to strongly affect solid electrolyte interphase stabilization and cyclic stability. When mixed with an optimal amount of 30 wt% pitch carbon, the SiOx showed a high charge/discharge cyclic stability of about 97% for the 2nd to the 50th cycle. The initial specific capacity of the SiOx was measured to be 1401 mAh/g. On the basis of the evaluation of the SiOx coating material, the process utilized in this study is considered an efficient method to produce SiOx with high performance in an economical way.

  14. 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.

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

    Institute of Scientific and Technical Information of China (English)

    Haifang Ni; Weili Song; Lizhen Fan n

    2016-01-01

    Spinel lithium titanate (Li4Ti5O12) has the advantages of structural stability, however it suffers the dis-advantages 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 re-lated to the synergistic effects of the CNTs matrix and the carbon-coating layers with conductivity en-hancement. Additionally, the amorphous carbon coating is an effective route to ameliorate the rate capability of Li4Ti5O12/CNTs.

  16. Unique Urchin-like Ca2Ge7O16 Hierarchical Hollow Microspheres as Anode Material for the Lithium Ion Battery

    OpenAIRE

    Dan Li; Chuanqi Feng; Hua Kun Liu; Zaiping Guo

    2015-01-01

    Germanium is an outstanding anode material in terms of electrochemical performance, especially rate capability, but its developments are hindered by its high price because it is rare in the crust of earth, and its huge volume variation during the lithium insertion and extraction. Introducing other cheaper elements into the germanium-based material is an efficient way to dilute the high price, but normally sacrifice its electrochemical performance. By the combination of nanostructure design an...

  17. Electrochemical characterization of carbon coated bundle-type silicon nanorod for anode material in lithium ion secondary batteries

    Energy Technology Data Exchange (ETDEWEB)

    Halim, Martin [Center for Energy Convergence, Korea Institute of Science and Technology, Hwarangno 14-gil 5, Seongbuk-gu, Seoul 136-791 (Korea, Republic of); Energy and Environmental Engineering, Korea University of Science and Technology, Gwahangno, Yuseong-gu, Daejeon, 305-333 (Korea, Republic of); Kim, Jung Sub [Center for Energy Convergence, Korea Institute of Science and Technology, Hwarangno 14-gil 5, Seongbuk-gu, Seoul 136-791 (Korea, Republic of); Department of Material Science & Engineering, Korea University, Seoul 136-713 (Korea, Republic of); Choi, Jeong-Gil [Department of Chemical Engineering, Hannam University, 461-1 Junmin-dong, Yusung-gu, Taejon 305-811 (Korea, Republic of); Lee, Joong Kee, E-mail: leejk@kist.re.kr [Center for Energy Convergence, Korea Institute of Science and Technology, Hwarangno 14-gil 5, Seongbuk-gu, Seoul 136-791 (Korea, Republic of); Energy and Environmental Engineering, Korea University of Science and Technology, Gwahangno, Yuseong-gu, Daejeon, 305-333 (Korea, Republic of)

    2015-04-15

    Highlights: • Bundle-type silicon nanorods (BSNR) were synthesized by metal assisted chemical etching. • Novel bundle-type nanorods electrode showed self-relaxant characteristics. • The self-relaxant property was enhanced by increasing the silver concentration. • PAA binder enhanced the self-relaxant property of the silicon material. • Carbon coated BSNR (BSNR@C) has evidently provided better cycle performance. - Abstract: Nanostructured silicon synthesis by surface modification of commercial micro-powder silicon was investigated in order to reduce the maximum volume change over cycle. The surface of micro-powder silicon was modified using an Ag metal-assisted chemical etching technique to produce nanostructured material in the form of bundle-type silicon nanorods. The volume change of the electrode using the nanostructured silicon during cycle was investigated using an in-situ dilatometer. Our result shows that nanostructured silicon synthesized using this method showed a self-relaxant characteristic as an anode material for lithium ion battery application. Moreover, binder selection plays a role in enhancing self-relaxant properties during delithiation via strong hydrogen interaction on the surface of the silicon material. The nanostructured silicon was then coated with carbon from propylene gas and showed higher capacity retention with the use of polyacrylic acid (PAA) binder. While the nano-size of the pore diameter control may significantly affect the capacity fading of nanostructured silicon, it can be mitigated via carbon coating, probably due to the prevention of Li ion penetration into 10 nano-meter sized pores.

  18. Effects of phosphorous incorporation on the microstructure of Si nanoparticles as an anode material for lithium-ion battery

    Energy Technology Data Exchange (ETDEWEB)

    Jung, Chun-young; Koo, Jeong-boon [Korea Institute of Energy Research, 152 Gajeong-ro, Yuseong-gu, Daejeon 304-343 (Korea, Republic of); Graduate School of Energy Science and Technology, Chungnam National University, 99 Deahak-ro Yuseong-gu, Daejeon 305-764 (Korea, Republic of); Jang, Bo-yun, E-mail: byjang@kier.re.kr [Korea Institute of Energy Research, 152 Gajeong-ro, Yuseong-gu, Daejeon 304-343 (Korea, Republic of); Kim, Joon-soo; Lee, Jin-seok [Korea Institute of Energy Research, 152 Gajeong-ro, Yuseong-gu, Daejeon 304-343 (Korea, Republic of); Kim, Sung-soo; Han, Moon-hee [Graduate School of Energy Science and Technology, Chungnam National University, 99 Deahak-ro Yuseong-gu, Daejeon 305-764 (Korea, Republic of)

    2015-07-31

    Si nanoparticles were synthesized by inductively coupled plasma and a specially designed double tube reactor. By injection of large amount of PH{sub 3} during the synthesis, the effects of phosphorous incorporation on their microstructures and chemical binding environments were investigated. Injection of PH{sub 3} gas during the synthesis resulted in a change from crystalline to amorphous phase, a reduction of particle size as well as a process yield. All of the above results were attributed to a lower plasma density when higher amount of PH{sub 3} was injected. From energy-dispersive X-ray spectroscopy, secondary ion mass spectrometry, and X-ray photoelectron spectroscopy analysis, it was revealed that P was doped in Si nanoparticles. However, secondary phases such as P{sub 4} and P{sub 2}O{sub 5} were formed as amorphous ones in nano-scale when a relatively large amount of PH{sub 3} was injected. In addition, those nanoparticles were applied as an active material in the lithium-ion battery's anode. Unexpectedly, amorphous Si nanoparticles with secondary phases showed improved electrochemical properties. P-doping in Si nanoparticles could not directly advance cycling performance by improvement of electrical conductivity of Si nanoparticles. It was rather assumed that a secondary phase influenced and enhanced electrochemical properties by additional capacity due to a formation of Li{sub 3}P and forming an effective buffer against large volumetric change of Si nanoparticles during the charge/discharge. The initial reversible capacity of amorphous Si nanoparticles synthesized with 100 sccm of PH{sub 3} flow rate was 2113 mAh g{sup −1}, and that at the 100th cycle was still about 1000 mAh g{sup −1}, which was twice as high as that of Si nanoparticles synthesized without PH{sub 3} injection. - Highlights: • Silicon nanoparticles with phosphorous were synthesized by inductively coupled plasma. • Effects of phosphorous incorporation on the microstructure

  19. Effects of phosphorous incorporation on the microstructure of Si nanoparticles as an anode material for lithium-ion battery

    International Nuclear Information System (INIS)

    Si nanoparticles were synthesized by inductively coupled plasma and a specially designed double tube reactor. By injection of large amount of PH3 during the synthesis, the effects of phosphorous incorporation on their microstructures and chemical binding environments were investigated. Injection of PH3 gas during the synthesis resulted in a change from crystalline to amorphous phase, a reduction of particle size as well as a process yield. All of the above results were attributed to a lower plasma density when higher amount of PH3 was injected. From energy-dispersive X-ray spectroscopy, secondary ion mass spectrometry, and X-ray photoelectron spectroscopy analysis, it was revealed that P was doped in Si nanoparticles. However, secondary phases such as P4 and P2O5 were formed as amorphous ones in nano-scale when a relatively large amount of PH3 was injected. In addition, those nanoparticles were applied as an active material in the lithium-ion battery's anode. Unexpectedly, amorphous Si nanoparticles with secondary phases showed improved electrochemical properties. P-doping in Si nanoparticles could not directly advance cycling performance by improvement of electrical conductivity of Si nanoparticles. It was rather assumed that a secondary phase influenced and enhanced electrochemical properties by additional capacity due to a formation of Li3P and forming an effective buffer against large volumetric change of Si nanoparticles during the charge/discharge. The initial reversible capacity of amorphous Si nanoparticles synthesized with 100 sccm of PH3 flow rate was 2113 mAh g−1, and that at the 100th cycle was still about 1000 mAh g−1, which was twice as high as that of Si nanoparticles synthesized without PH3 injection. - Highlights: • Silicon nanoparticles with phosphorous were synthesized by inductively coupled plasma. • Effects of phosphorous incorporation on the microstructure were studied. • Silicon nanoparticles were applied as an anode material

  20. In Situ Hydrothermal Synthesis of Mn3O4 Nanoparticles on Nitrogen-doped Graphene as High-Performance Anode materials for Lithium Ion Batteries

    International Nuclear Information System (INIS)

    Highlights: • We present a facile process to synthesize Mn3O4/N-doped graphene hybrid materials by hydrothermal route. • Mn3O4/N-doped graphene hybrid materials exhibit a large reversible capacity of about 828 mA h g−1 after 40 cycles. • Mn3O4/graphene hybrid materials demonstrate great potential for lithium ion battery anodes. - Abstract: Developing new electrode materials with high specific capacity for excellent lithium ion storage properties is very desirable. In this paper, we introduce a simple hydrothermal method for the growth of Mn3O4 nanoparticles onto nitrogen-doped graphene (N-doped graphene) for high-performance lithium ion battery (LIB) anodes. Hydrazine plays a fundamental role in the formation of such nanostructures as it can act both as a reducing agent and as a nitrogen source. In the synthesized composite, highly crystalline Mn3O4 nanoparticles with average sizes of 20–50 nm are homogeneously dispersed on both sides of the N-doped graphene. The nitrogen content in the doped graphene is confirmed by elemental analyzer, and 2 wt% of the sample is found to be composed of nitrogen element. The as-prepared Mn3O4/N-doped graphene composites exhibit remarkable electrochemical performance, including high reversible specific capacity, outstanding cycling stability, and excellent rate capability (approximately 400 mA h g−1 at 2.0 A g−1) when used as the anode material for LIBs. The improvement in the electrochemical properties of the material can be attributed to graphene, which acts as both an electron conductor and a volume buffer layer, and nitrogen doping allows for fast electron and ion transfer by decreasing the energy barrier. This type of metal oxide/N-doped graphene composites can be promising candidates for high-performance anode materials for LIBs

  1. Corrosion rate of construction materials in hot phosphoric acid with the contribution of anodic polarization

    DEFF Research Database (Denmark)

    Kouril, M.; Christensen, Erik; Eriksen, S.;

    2011-01-01

    ). Several grades of stainless steels were tested as well as tantalum, niobium, titanium, nickel alloys and silicon carbide. The corrosion rate was evaluated by means of mass loss at free corrosion potential as well as under various levels of polarization. The only corrosion resistant material in 85...

  2. Solid state cathode materials for secondary magnesium-ion batteries that are compatible with magnesium metal anodes in water-free electrolyte

    Science.gov (United States)

    Crowe, Adam J.; Bartlett, Bart M.

    2016-10-01

    With high elemental abundance, large volumetric capacity, and dendrite-free metal deposition, magnesium metal anodes offer promise in beyond-lithium-ion batteries. However, the increased charge density associated with the divalent magnesium-ion (Mg2+), relative to lithium-ion (Li+) hinders the ion-insertion and extraction processes within many materials and structures known for lithium-ion cathodes. As a result, many recent investigations incorporate known amounts of water within the electrolyte to provide temporary solvation of the Mg2+, improving diffusion kinetics. Unfortunately with the addition of water, compatibility with magnesium metal anodes disappears due to forming an ion-insulating passivating layer. In this short review, recent advances in solid state cathode materials for rechargeable magnesium-ion batteries are highlighted, with a focus on cathode materials that do not require water contaminated electrolyte solutions for ion insertion and extraction processes.

  3. 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. PMID:27406922

  4. Research Progress in Anode Materials for Lithium Ion Batteries%锂离子电池新型负极材料的研究进展

    Institute of Scientific and Technical Information of China (English)

    刘浪浪; 问娟娟

    2014-01-01

    锂离子电池作为一种电源应用很广泛,但是在应用中存在一些不足,选取电化学性能良好的正负极材料是提高和改善锂离子电池电化学性能最重要的因素。从新型碳材料、硅基负极材料、锡基负极材料三方面介绍了目前锂离子电池的研究状况,并展望了锂离子电池负极材料的发展趋势。%Lithium ion battery as a power is widely used, but there are some deficiencies in the application. Selection of electrode materials with excellent electrochemical performances is the key factor to enhance and improve the electrochemical performance of the lithium ion battery. In this paper, the current research situation of lithium ion batteries were introduced from the aspects of new carbon materials, silicon-based anode materials and tin-based anode materials, and the development trend of the anode materials for lithium ion battery was prospected.

  5. Si-Based Materials as the Anode of Lithium-Ion Batteries%锂离子电池负极硅基材料

    Institute of Scientific and Technical Information of China (English)

    陶占良; 王洪波; 陈军

    2011-01-01

    硅基材料由于其高电化学容量是一种非常有发展前途的锂离子电池负极材料,但其在充放电过程中体积变化大、循环寿命差、首次库仑效率低等是阻碍其商业化的主要问题.本文综述了硅在脱嵌锂时晶体结构及表/界面的变化,以及改善其电化学性能方面的研究进展,并阐述其作为锂离子电池负极材料的研究前景.%Silicon-based materials are promising anode materials for lithium-ion batteries (LIBs) due to their high-energy capacity. However, the commercialization of silicon-based materials as the anode of LIBs has been hindered by the huge volume change, poor cycle life and low initial coulombic efficiency during the charge/discharge process. This article reviews the change of both the crystal structure and the surface/interface of Si-based material during the interealation/deintercalation of lithium, and the methods improving the electrochemical performance. In addition, the prospects of silicon-based materials as the anode of LIBs are also discussed.

  6. Pyrolyzed bacterial cellulose: a versatile support for lithium ion battery anode materials.

    Science.gov (United States)

    Wang, Bin; Li, Xianglong; Luo, Bin; Yang, Jingxuan; Wang, Xiangjun; Song, Qi; Chen, Shiyan; Zhi, Linjie

    2013-07-22

    A scalable, low-cost and environmentally benign strategy is developed for the facile construction of a unique kind of three-dimensional porous electrode architecture for high-performance lithium ion batteries. The methodology is based on the employment of pyrolyzed bacterial cellulose as a new three-dimensional porous scaffold to support various nanostructured active electrode materials, such as SnO2 and Ge.

  7. Synthesis of Nanocobalt Powders for an Anode Material of Lithium-Ion Batteries by Chemical Reduction and Carbon Coating

    Directory of Open Access Journals (Sweden)

    Seong-Hyeon Hong

    2014-01-01

    Full Text Available Nanosized Co powders were prepared by a chemical reduction method with and without CTAB (cetyltrimethylammonium bromide, C19H42BrN and carbon-coating heat treatment at 700°C for 1 h, and the electrochemical properties of the prepared nanosized Co powders were examined to evaluate their suitability as an anode material of Li-ion batteries. Nanosized amorphous Co-based powders could be synthesized by a chemical reduction method in which a reducing agent is added to a Co ion-dissolved aqueous solution. When the prepared nanosized Co-based powders were subjected to carbon-coating heat treatment at 700°C for 1 h, the amorphous phase was crystallized, and a Co single phase could be obtained. The Co-based powder prepared by chemical reduction with CTAB and carbon-coating heat treatment had a smaller first discharge capacity (about 557 mAh/g than the Co-based powder prepared by chemical reduction without CTAB and carbon-coating heat treatment (about 628 mAh/g. However, the former had a better cycling performance than the latter from the third cycle. The carbon-coated layers are believed to have led to quite good cycling performances of the prepared Co-based powders from the third cycle.

  8. Preparation and electrochemical performances of cubic shape Cu2O as anode material for lithium ion batteries

    International Nuclear Information System (INIS)

    Cubic and star-shaped crystalline Cu2O particles were synthesized by reducing the copper citrate complex solution with glucose. The microstructure and morphology of the Cu2O were characterized by means of X-ray diffraction (XRD) and scanning electron microscopy (SEM). The electrochemical properties of the Cu2O as anode materials for lithium ion batteries were measured by galvanostatic charge-discharge tests. The as-synthesized Cu2O particles were 1-2 μm with narrow distribution and the shape of Cu2O particles had an effect on the electrochemical properties. The cubic Cu2O particles delivered a higher reversible discharge capacity (390 mAh g-1) than the star-shaped Cu2O, and also exhibited good cyclability. The star-shaped Cu2O particles presented poor cyclability due to pulverization and deterioration after cycling, but the morphology of the cubic Cu2O particles was stable even after 50 cycles

  9. AB5-type Hydrogen Storage Alloy Modified with Ti/Zr Used as Anodic Materials in Borohydride Fuel Cell

    Institute of Scientific and Technical Information of China (English)

    Lianbang WANG; Chunan MA; Xinbiao MAO; Yuanming SUN; Seijiro SUDA

    2005-01-01

    Fuel cell using borohydride as the fuel has received much attention. AB5-type hydrogen storage alloy used as the anodic material instead of noble metals has been investigated. In order to restrain the generation of hydrogen and enhance the utilization of borohydride, Ti/Zr metal powders has been added into the parent LmNi4.78Mn0.22 (where Lm is La-richened mischmetal) alloy (LNM) by ball milling and heat treatment methods. It is found that the addition of Ti/Zr metal powders lowers the electrochemical catalytic activity of the electrodes, at the same time, restrains the generation of hydrogen and enhances the utilization of the fuel. All the results show that the hydrogen generation rate or the utilization of the fuel is directly relative to the electrochemical catalytic activity or the discharge capability of the electrodes. The utilization of the fuel increases with discharge current density. It is very important to find a balance between the discharge capability and the utilization of the fuel.

  10. A comparative study of electrochemical properties of two kinds of carbon nanotubes as anode materials for lithium ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Yang, Shubin; Huo, Junping; Song, Huaihe; Chen, Xiaohong [State Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology, 100029 Beijing (China)

    2008-01-01

    Two kinds of carbon nanotubes (CNTs), i.e., short carbon nanotubes (CNTs-1) synthesized by co-pyrolysis method and long carbon nanotubes (CNTs-2) produced using common CVD technique were comparatively investigated as anode materials for lithium ion batteries via transmission electron microscope (TEM), high-resolution TEM and a variety of electrochemical testing techniques. The test results showed that the reversible capacities of CNTs-1 electrode were 266 and 170 mAh g{sup -1} at the current densities of 0.2 and 0.8 mA cm{sup -2}, respectively, which were almost twice those of CNTs-2 electrode. The larger voltage hysteresis in CNTs-2 electrode was not only related to the surface functional groups on CNTs, but also to the surface resistance of CNTs, which results in greater hindrance and higher overvoltage during lithium extraction from electrode. The kinetics properties of these two CNTs electrodes were compared by AC impedance measurements. It was found that, both the surface film and charge-transfer resistances of CNTs-1 were significantly lower than those of CNTs-2; the lithium diffusion coefficient (D{sub Li}) of both CNTs electrodes decreased as the drop of voltage, but the magnitude of the D{sub Li} variation of CNTs-1 electrode was smaller than that of CNTs-2 electrode, indicating CNTs-1 exhibited higher electrochemical activity and more favorable kinetic properties during charge and discharge process. (author)

  11. A comparative study of electrochemical properties of two kinds of carbon nanotubes as anode materials for lithium ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Yang Shubin; Huo Junping [State Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology, 100029 Beijing (China); Song Huaihe [State Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology, 100029 Beijing (China)], E-mail: songhh@mail.buct.edu.cn; Chen Xiaohong [State Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology, 100029 Beijing (China)

    2008-01-01

    Two kinds of carbon nanotubes (CNTs), i.e., short carbon nanotubes (CNTs-1) synthesized by co-pyrolysis method and long carbon nanotubes (CNTs-2) produced using common CVD technique were comparatively investigated as anode materials for lithium ion batteries via transmission electron microscope (TEM), high-resolution TEM and a variety of electrochemical testing techniques. The test results showed that the reversible capacities of CNTs-1 electrode were 266 and 170 mAh g{sup -1} at the current densities of 0.2 and 0.8 mA cm{sup -2}, respectively, which were almost twice those of CNTs-2 electrode. The larger voltage hysteresis in CNTs-2 electrode was not only related to the surface functional groups on CNTs, but also to the surface resistance of CNTs, which results in greater hindrance and higher overvoltage during lithium extraction from electrode. The kinetics properties of these two CNTs electrodes were compared by AC impedance measurements. It was found that, both the surface film and charge-transfer resistances of CNTs-1 were significantly lower than those of CNTs-2; the lithium diffusion coefficient (D{sub Li}) of both CNTs electrodes decreased as the drop of voltage, but the magnitude of the D{sub Li} variation of CNTs-1 electrode was smaller than that of CNTs-2 electrode, indicating CNTs-1 exhibited higher electrochemical activity and more favorable kinetic properties during charge and discharge process.

  12. Micro-sized and Nano-sized Fe3O4 Particles as Anode Materials for Lithium-ion Batteries

    Institute of Scientific and Technical Information of China (English)

    Y.X.Chen; L.H.He; P.J.Shang; Q.L.Tang; Z.Q.Liu; H.B.Liu; L.P.Zhou

    2011-01-01

    Micro-sized (1030.3±178.4 nm) and nano-sized (50.4±8.0 nm) Fe3O4 particles have been fabricated through hydrogen thermal reduction of α-Fe2O3 particles synthesized by means of a hydrothermal process. The morphology and microstructure of the micro-sized and the nano-sized Fe3O4 particles were characterized by X-ray diffraction, field-emission gun scanning electron microscopy, transmission electron microscopy and highresolution electron microscopy. The micro-sized Fe3O4 particles exhibit porous structure, while the nano-sized Fe3O4 particles are solid structure. Their electrochemical performance was also evaluated. The nano-sized solid Fe3O4 particles exhibit gradual capacity fading with initial discharge capacity of 1083.1 mAhg-1 and reversible capacity retention of 32.6% over 50 cycles. Interestingly, the micro-sized porous Fe3O4 particles display very stable capacity-cycling behavior, with initial discharge capacity of 887.5 mAhg-1 and charge capacity of 684.4 mAhg-1 at the 50th cycle. Therefore, 77.1% of the reversible capacity can be maintained over 50 cycles. The micro-sized porous Fe3O4 particles with facile synthesis, good cycling performance and high capacity retention are promising candidate as anode materials for high energy-density lithium-ion batteries.

  13. Enhancement of electrochemical performance with Zn-Al-Bi layered hydrotalcites as anode material for Zn/Ni secondary battery

    International Nuclear Information System (INIS)

    Bi-doped Zn-Al layered double hydroxides (Zn-Al-Bi LDH) are prepared by the constant pH hydrothermal method and proposed as a novel anodic material in Zn/Ni secondary cells. The Fourier transform infrared spectra (FT-IR), X-ray diffraction (XRD), scanning electron microscopy (SEM) images reveal that the as-prepared samples are well-crystallized and hexagon layer structure. The electrochemical performances of the Zn-Al-Bi LDH were analyzed by cyclic voltammetry, tafel plot, electrochemical impedance spectroscopy (EIS) and galvanostatic charge-discharge tests. Compared with Zn-Al LDH, Zn-Al-Bi LDH with different Zn/Al/Bi molar rations, especially the sample of Zn/Al/Bi = 3:0.8:0.2 (molar ration) have higher discharge capacity and more stable cycling performances. Cyclic voltammograms clearly illuminated that the Zn-Al-Bi LDHs could decrease polarization, maintain the electrochemical activity, and enhance the discharge capacity of Zn-Al LDH. This battery can undergo at least 800 charge-discharge cycles at constant current of 1C without dendrite and short circuits. The discharge capacity of Zn-Al-Bi LDH after the 800th cycle remains about 380 mAh g−1 and the hexagonal crystal structure have no much changed after cycles

  14. One-Pot Synthesis of SnO2/C Nanocapsules Composites as Anode Materials for Lithium-Ion Batteries.

    Science.gov (United States)

    Yang, Lina; Chen, Kexun; Dong, Tao; Wang, Zhao; Li, Guomin; Zhang, Yanling; Zhang, Lipeng

    2016-02-01

    In this work, we demonstrate a facile route for the synthesis of nanostructured SnO2/C composites for lithium-ion batteries. The anode materials were prepared via a one-pot solvothermal approach and then calcination in a highly pure nitrogen atmosphere. The composited was composed of amor- phous carbon and nanocrystalline SnO2 by the X-ray diffraction (XRD) analysis, and the content of carbon was calculated according to the thermogravimetric analysis (TGA). Scanning electron microscopy (SEM) images revealed that the diameter of these as-prepared spheres varied from 50 to 60 nm. A systematic study has been carried out to examine the effect of carbon content upon lithium-ion battery performance. The electrochemical results showed that SnO2/C nanocomposite could achieve 1197.5 mAh/g reversible capacity and 55.11% initial coulombic efficiency, and 190% capacity retention after 50 cycles compared to the SnO2 nanoparticles of 940.6 mAh/g at a current density 0.2 C in the voltage range of 0.01-3.0 V. These improvements can be ascribed to the carbon, which can enhance the conductivity of SnO2, suppress the aggregation of active particles, and increase their structural stability during cycling. PMID:27433668

  15. Ultrafine Nb2O5 Nanocrystal Coating on Reduced Graphene Oxide as Anode Material for High Performance Sodium Ion Battery.

    Science.gov (United States)

    Yan, Litao; Chen, Gen; Sarker, Swagotom; Richins, Stephanie; Wang, Huiqiang; Xu, Weichuan; Rui, Xianhong; Luo, Hongmei

    2016-08-31

    Ultrafine niobium oxide nanocrystals/reduced graphene oxide (Nb2O5 NCs/rGO) was demonstrated as a promising anode material for sodium ion battery with high rate performance and high cycle durability. Nb2O5 NCs/rGO was synthesized by controllable hydrolysis of niobium ethoxide and followed by heat treatment at 450 °C in flowing forming gas. Transmission electron microscopy images showed that Nb2O5 NCs with average particle size of 3 nm were uniformly deposited on rGO sheets and voids among Nb2O5 NCs existed. The architecture of ultrafine Nb2O5 NCs anchored on a highly conductive rGO network can not only enhance charge transfer and buffer the volume change during sodiation/desodiation process but also provide more active surface area for sodium ion storage, resulting in superior rate and cycle performance. Ex situ XPS analysis revealed that the sodium ion storage mechanism in Nb2O5 could be accompanied by Nb(5+)/Nb(4+) redox reaction and the ultrafine Nb2O5 NCs provide more surface area to accomplish the redox reaction.

  16. Aerosol assisted synthesis of hierarchical tin–carbon composites and their application as lithium battery anode materials

    KAUST Repository

    Guo, Juchen

    2013-01-01

    We report a method for synthesizing hierarchically structured tin-carbon (Sn-C) composites via aerosol spray pyrolysis. In this method, an aqueous precursor solution containing tin(ii) chloride and sucrose is atomized, and the resultant aerosol droplets carried by an inert gas are pyrolyzed in a high-temperature tubular furnace. Owing to the unique combination of high reaction temperature and short reaction time, this method is able to achieve a hetero-structure in which small Sn particles (15 nm) are uniformly embedded in a secondary carbon particle. This procedure allows the size and size distribution of the primary Sn particles to be tuned, as well as control over the size of the secondary carbon particles by addition of polymeric surfactant in the precursor solution. When evaluated as anode materials for lithium-ion batteries, the resultant Sn-C composites demonstrate attractive electrochemical performance in terms of overall capacity, electrochemical stability, and coulombic efficiency. © 2013 The Royal Society of Chemistry.

  17. Ultrafine Nb2O5 Nanocrystal Coating on Reduced Graphene Oxide as Anode Material for High Performance Sodium Ion Battery.

    Science.gov (United States)

    Yan, Litao; Chen, Gen; Sarker, Swagotom; Richins, Stephanie; Wang, Huiqiang; Xu, Weichuan; Rui, Xianhong; Luo, Hongmei

    2016-08-31

    Ultrafine niobium oxide nanocrystals/reduced graphene oxide (Nb2O5 NCs/rGO) was demonstrated as a promising anode material for sodium ion battery with high rate performance and high cycle durability. Nb2O5 NCs/rGO was synthesized by controllable hydrolysis of niobium ethoxide and followed by heat treatment at 450 °C in flowing forming gas. Transmission electron microscopy images showed that Nb2O5 NCs with average particle size of 3 nm were uniformly deposited on rGO sheets and voids among Nb2O5 NCs existed. The architecture of ultrafine Nb2O5 NCs anchored on a highly conductive rGO network can not only enhance charge transfer and buffer the volume change during sodiation/desodiation process but also provide more active surface area for sodium ion storage, resulting in superior rate and cycle performance. Ex situ XPS analysis revealed that the sodium ion storage mechanism in Nb2O5 could be accompanied by Nb(5+)/Nb(4+) redox reaction and the ultrafine Nb2O5 NCs provide more surface area to accomplish the redox reaction. PMID:27508452

  18. Synthesis and Characterization of Silicon Nanoparticles Inserted into Graphene Sheets as High Performance Anode Material for Lithium Ion Batteries

    Directory of Open Access Journals (Sweden)

    Yong Chen

    2014-01-01

    Full Text Available Silicon nanoparticles have been successfully inserted into graphene sheets via a novel method combining freeze-drying and thermal reduction. The structure, electrochemical performance, and cycling stability of this anode material were characterized by SEM, X-ray diffraction (XRD, charge/discharge cycling, and cyclic voltammetry (CV. CV showed that the Si/graphene nanocomposite exhibits remarkably enhanced cycling performance and rate performance compared with bare Si nanoparticles for lithium ion batteries. XRD and SEM showed that silicon nanoparticles inserted into graphene sheets were homogeneous and had better layered structure than the bare silicon nanoparticles. Graphene sheets improved high rate discharge capacity and long cycle-life performance. The initial capacity of the Si nanoparticles/graphene keeps above 850 mAhg−1 after 100 cycles at a rate of 100 mAg−1. The excellent cycle performances are caused by the good structure of the composites, which ensured uniform electronic conducting sheet and intensified the cohesion force of binder and collector, respectively.

  19. Micro- and nanomorphology coexisting in titanium dioxide coating for application as anode material in secondary lithium-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Lo, Wen-Chi, E-mail: wenchilo694@gmail.com; Chu, Hou-Jen; He, Ju-Liang

    2015-03-31

    Titanium dioxide has recently attracted attention as an anode material for use in lithium-ion batteries, owing to its high reversible capacity and durable charge/discharge characteristics. The aim of the study is to combine micro-arc oxidation (MAO) and post-alkali treatment to realize an anatase titanium dioxide (TiO{sub 2}) scaffold layer on titanium plates. Using this combination, coexisting micro- and nanomorphology can be realized in the TiO{sub 2} layer. This increases the specific surface area of the TiO{sub 2} layer and thereby improves the charge capacity and charge/discharge rate of the anode. The effectiveness of MAO to fabricate a micrometer-scale porous TiO{sub 2} structure on titanium plate, and the formation of nano-flakes by alkali treatment on porous anatase TiO{sub 2} layer was demonstrated. Further, numerous 40–80 nm alkali-treatment-induced nano-flakes grew all over the oxide surface, substantially increasing its specific surface area. The measured electrochemical properties demonstrate that at potentials of − 1.98 V and − 0.56 V vs. Ag/AgCl, lithium ions were respectively inserted into and extracted from the TiO{sub 2} layer with nano-flakes. The nano-flakes promote faster lithium-ion insertion and extraction and higher associated number of charge than the MAO TiO{sub 2}. The detailed charging/discharging kinetic processes of the MAO, annealed MAO, alkali-treated MAO, and annealed and alkali-treated MAO specimens were determined using electrochemical impedance spectroscopy, thus providing further insight into the performance of the TiO{sub 2} coating. - Highlights: • A micrometer-scale porous crystalline TiO{sub 2} layer was fabricated by MAO. • After alkali treatment, the oxide surface exhibits numerous pores. • The layer was composed of predominantly anatase and minor rutile. • Optimum solution temperature and NaOH concentration yielded nano-flaky morphology. • Such morphology leads to the increase performance of the treated

  20. Micro- and nanomorphology coexisting in titanium dioxide coating for application as anode material in secondary lithium-ion batteries

    International Nuclear Information System (INIS)

    Titanium dioxide has recently attracted attention as an anode material for use in lithium-ion batteries, owing to its high reversible capacity and durable charge/discharge characteristics. The aim of the study is to combine micro-arc oxidation (MAO) and post-alkali treatment to realize an anatase titanium dioxide (TiO2) scaffold layer on titanium plates. Using this combination, coexisting micro- and nanomorphology can be realized in the TiO2 layer. This increases the specific surface area of the TiO2 layer and thereby improves the charge capacity and charge/discharge rate of the anode. The effectiveness of MAO to fabricate a micrometer-scale porous TiO2 structure on titanium plate, and the formation of nano-flakes by alkali treatment on porous anatase TiO2 layer was demonstrated. Further, numerous 40–80 nm alkali-treatment-induced nano-flakes grew all over the oxide surface, substantially increasing its specific surface area. The measured electrochemical properties demonstrate that at potentials of − 1.98 V and − 0.56 V vs. Ag/AgCl, lithium ions were respectively inserted into and extracted from the TiO2 layer with nano-flakes. The nano-flakes promote faster lithium-ion insertion and extraction and higher associated number of charge than the MAO TiO2. The detailed charging/discharging kinetic processes of the MAO, annealed MAO, alkali-treated MAO, and annealed and alkali-treated MAO specimens were determined using electrochemical impedance spectroscopy, thus providing further insight into the performance of the TiO2 coating. - Highlights: • A micrometer-scale porous crystalline TiO2 layer was fabricated by MAO. • After alkali treatment, the oxide surface exhibits numerous pores. • The layer was composed of predominantly anatase and minor rutile. • Optimum solution temperature and NaOH concentration yielded nano-flaky morphology. • Such morphology leads to the increase performance of the treated Ti plate

  1. Relationship between anode material, supporting electrolyte and current density during electrochemical degradation of organic compounds in water

    Energy Technology Data Exchange (ETDEWEB)

    Guzmán-Duque, Fernando L. [Grupo de diagnóstico y control de la contaminación, Facultad de ingeniería, Universidad de Antioquia, A.A. 1226, Medellín (Colombia); Palma-Goyes, Ricardo E. [Grupo de Investigación en Remediación Ambiental y Biocatálisis, Instituto de Química, Facultad de Ciencias Exactas y Naturales, Universidad de Antioquía Udea, A.A. 1226, Medellín (Colombia); González, Ignacio [Universidad Autónoma Metropolitana-Iztapalapa, Departamento de Química, Av. San Rafael Atlixco No 186, C.P 09340, México D.F (Mexico); Peñuela, Gustavo [Grupo de diagnóstico y control de la contaminación, Facultad de ingeniería, Universidad de Antioquia, A.A. 1226, Medellín (Colombia); Torres-Palma, Ricardo A., E-mail: rtorres@matematicas.udea.edu.co [Grupo de Investigación en Remediación Ambiental y Biocatálisis, Instituto de Química, Facultad de Ciencias Exactas y Naturales, Universidad de Antioquía Udea, A.A. 1226, Medellín (Colombia)

    2014-08-15

    Highlights: • Pathway and efficiency are linked to the current-electrode–electrolyte interaction. • Unlike BDD, IrO{sub 2} route was independent of current but dependent on the electrolyte. • IrO{sub 2}/SO{sub 4}{sup 2−} and IrO{sub 2}/Cl{sup −} routes were via IrO{sub 3} and chlorine species, respectively. • BDD/SO{sub 4}{sup 2−} and IrO{sub 2}/Cl{sup −} systems were favored at low and high currents, respectively. - Abstract: Taking crystal violet (CV) dye as pollutant model, the electrode, electrolyte and current density (i) relationship for electro-degrading organic molecules is discussed. Boron-doped diamond (BDD) or Iridium dioxide (IrO{sub 2}) used as anode materials were tested with Na{sub 2}SO{sub 4} or NaCl as electrolytes. CV degradation and generated oxidants showed that degradation pathways and efficiency are strongly linked to the current density-electrode–electrolyte interaction. With BDD, the degradation pathway depends on i: If i < the limiting current density (i{sub lim}), CV is mainly degraded by ·OH radicals, whereas if i > i{sub lim}, generated oxidants play a major role in the CV elimination. When IrO{sub 2} was used, CV removal was not dependent on i, but on the electrolyte. Pollutant degradation in Na{sub 2}SO{sub 4} on IrO{sub 2} seems to occur via IrO{sub 3}; however, in the presence of NaCl, degradation was dependent on the chlorinated oxidative species generated. In terms of efficiency, the Na{sub 2}SO{sub 4} electrolyte showed better results than NaCl when BDD anodes were employed. On the contrary, NaCl was superior when combined with IrO{sub 2}. Thus, the IrO{sub 2}/Cl{sup −} and BDD/SO{sub 4}{sup 2−} systems were better at removing the pollutant, being the former the most effective. On the other hand, pollutant degradation with the BDD/SO{sub 4}{sup 2−} and IrO{sub 2}/Cl{sup −} systems is favored at low and high current densities, respectively.

  2. CoSb3-graphite composite anode material for lithium ion batteries

    Institute of Scientific and Technical Information of China (English)

    XIE Jian; CAO Gaoshao; ZHAO Xinbing

    2005-01-01

    The CoSb3-graphite composite was prepared by ball-milling. The electrochemical performance of the composite material was evaluated using the lithium ion model cell Li / LiPF6 (EC + DMC) / CoSb3C4. It was found that the CoSb3C4 composite shows higher reversible capacity than the pure CoSb3 alloy, and its first reversible (Li-ions removal) capacity reaches 721 Ma·h·g-1, which exceeds the theoretical capacity (550 Ma.h.g-1) of CoSb3C4.

  3. Hard carbon as anode material in lithium batteries: Synthesis and characterization

    Energy Technology Data Exchange (ETDEWEB)

    Baertsch, M.C.; Schmid, L.; Baiker, A.; Novak, P.

    2003-03-01

    Hard carbon is a possible alternative as negative electrode material for rechargeable lithium-ion batteries. A fast production of hard carbon can be reached if the curing time of the precursor is short. Due to the promising results from literature regarding epoxy resin as precursor we produced hard carbon from a commercially available fast-setting epoxy resin. The surface area and pore structure properties of the carbon powder were investigated with gas adsorption methods. The carbon particle size distribution was ana-lysed with a laser diffraction instrument. (author)

  4. Tantalum carbide as a novel support material for anode electrocatalysts in polymer electrolyte membrane water electrolysers

    DEFF Research Database (Denmark)

    Polonský, Jakub; Petrushina, Irina; Christensen, Erik;

    2012-01-01

    in a mixture of trifluoromethanesulfonic acid (TFMSA) and hydrogen peroxide at 130 °C. The liquid phase was subsequently analysed using ICP-MS with respect to the occurrence of ions potentially originating from the support material tested. The TaC support selected was additionally characterised...... and was equal to 0.1, 0.3, 0.5, 0.7, 0.9 and 1. The thin-film method was used for electrochemical characterisation of the electrocatalysts prepared. SEM–EDX analysis, X-ray diffraction, N2 adsorption (BET) and powder conductivity measurements were used as complementary techniques to complete characterisation...

  5. SnSe/carbon nanocomposite synthesized by high energy ball milling as an anode material for sodium-ion and lithium-ion batteries

    International Nuclear Information System (INIS)

    Graphical abstract: A homogeneous nanocomposite of SnSe and carbon black was synthesised by high energy ball milling and empolyed as an anode material for sodium-ion batteries (SIBs) and lithium-ion batteries (LIBs). The nanocomposite anode exhibits excellent electrochemical performances in both SIBs and LIBs. - Highlights: • A homogeneous nanocomposite of SnSe and carbon black was fabricated by high energy ball milling. • SnSe and carbon black are homogeneously mixed at the nanoscale level. • The SnSe/C anode exhibits excellent electrochemical performances in both SIBs and LIBs. - Abstract: A homogeneous nanocomposite of SnSe and carbon black, denoted as SnSe/C nanocomposite, was fabricated by high energy ball milling and empolyed as a high performance anode material for both sodium-ion batteries and lithium-ion batteries. The X-ray diffraction patterns, scanning electron microscopy and transmission electron microscopy observations confirmed that SnSe in SnSe/C nanocomposite was homogeneously distributed within carbon black. The nanocomposite anode exhibited enhanced electrochemical performances including a high capacity, long cycling behavior and good rate performance in both sodium-ion batteries (SIBs) and lithium-ion batteries (LIBs). In SIBs, an initial capacitiy of 748.5 mAh g−1 was obtained and was maintained well on cycling (324.9 mAh g−1 at a high current density of 500 mA g−1 in the 200 th cycle) with 72.5% retention of second cycle capacity (447.7 mAh g−1). In LIBs, high initial capacities of approximately 1097.6 mAh g−1 was obtained, and this reduced to 633.1 mAh g−1 after 100 cycles at 500 mA g−1

  6. 3D Fe{sub 2}(MoO{sub 4}){sub 3} microspheres with nanosheet constituents as high-capacity anode materials for lithium-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Zheng, Hao; Wang, Shiqiang [Hubei University, Key Laboratory for Synthesis and Applications of Organic Functional Molecules (China); Wang, Jiazhao; Wang, Jun [University of Wollongong, Institute for Superconducting and Electronic Materials (Australia); Li, Lin; Yang, Yun; Feng, Chuanqi, E-mail: cfeng@hubu.edu.cn [Hubei University, Key Laboratory for Synthesis and Applications of Organic Functional Molecules (China); Sun, Ziqi, E-mail: ziqi.sun@qut.edu.au [Queensland University of Technology, School of Chemistry, Physics and Mechanical Engineering, Science and Engineering Faculty (Australia)

    2015-11-15

    Three-dimensional (3D) Fe{sub 2}(MoO{sub 4}){sub 3} microspheres with ultrathin nanosheet constituents are first synthesized as anode materials for the lithium-ion battery. It is interesting that the single-crystalline nanosheets allow rapid electron/ion transport on the inside, and the high porosity ensures fast diffusion of liquid electrolyte in energy storage applications. The electrochemical properties of Fe{sub 2}(MoO{sub 4}){sub 3} as anode demonstrates that 3D Fe{sub 2}(MoO{sub 4}){sub 3} microspheres deliver an initial capacity of 1855 mAh/g at a current density of 100 mA/g. Particularly, when the current density is increased to 800 mA/g, the reversible capacity of Fe{sub 2}(MoO{sub 4}){sub 3} anode still arrived at 456 mAh/g over 50 cycles. The large and reversible capacities and stable charge–discharge cycling performance indicate that Fe{sub 2}(MoO{sub 4}){sub 3} is a promising anode material for lithium battery applications.Graphical abstractThe electrochemical properties of Fe{sub 2}(MoO{sub 4}){sub 3} as anode demonstrates that 3D Fe{sub 2}(MoO{sub 4}){sub 3} microspheres delivered an initial capacity of 1855 mAh/g at a current density of 100 mA/g. When the current density was increased to 800 mA/g, the Fe{sub 2}(MoO{sub 4}){sub 3} still behaved high reversible capacity and good cycle performance.

  7. Mesoporous silicon/carbon hybrids with ordered pore channel retention and tunable carbon incorporated content as high performance anode materials for lithium-ion batteries

    International Nuclear Information System (INIS)

    In-situ magnesiothermic reduction reaction route was developed to synthesize mesoporous Si/C (silicon/carbon) hybrids with ordered pore channel retention and tunable carbon incorporated content as high performance anode materials for LIBs (lithium ion batteries). The effect of carbon incorporation on the microstructures and electrochemical performance of the Si/C hybrid LIBs anodes is investigated. The incorporation of carbon in the Si/C hybrids not only prevents the ordered structure of mesoporous silicon from collapsing, but also increases the electrical conductivity of the synthesized Si/C hybrids. The as-prepared Si/C hybrid LIBs anode with an optimal carbon content of 7.05 wt%, displays improved electrochemical performance with a high reversible specific capacity, rate capability and excellent cyclic performance, showing a higher specific capacity of up to 1452 mAh g−1 at a current density of 200 mA g−1 after 100 cycles and a high coulombic efficiency of up to 99.2%. The great improvement of the electrochemical performance of the ordered mesoporous Si/C hybrid LIBs anodes can be attributed to the unique ordered structure, large surface area, the homogeneously incorporated carbon in the Si/C hybrids. The synthesized ordered mesoporous Si/C hybrids are promising for potential applications as LIB anode materials with enhanced electrochemical performance. - Highlights: • Ordered mesoporous Si/C hybrids are synthesized by chemically reducing silica. • The pre-impregnated carbon source prevents the ordered structure from collapsing. • Mesoporous Si/C hybrids exhibit excellent Li+ storage capacity and cyclic stability

  8. One-pot synthesis of nitrogen and sulfur co-doped graphene supported MoS2 as high performance anode materials for lithium-ion batteries

    International Nuclear Information System (INIS)

    Highlights: • Nitrogen and sulfur co-doped graphene supported MoS2 nanosheets were successfully prepared and used as anode materials for Li-ion batteries. • The as-prepared anode materials show excellent stability in Li-ion batteries. • The materials show high reversible capacity for lithium ion batteries. - Abstract: Nitrogen and sulfur co-doped graphene supported MoS2 (MoS2/NS-G) nanosheets were prepared through a one-pot thermal annealing method. The as prepared samples were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), Raman spectra and electrochemical techniques. The MoS2/NS-G shows high reversible capacity about 1200 mAh/g at current density of 150 mA/g and excellent stability in Li-ion batteries. It was demonstrated the co-doping of graphene by N and S could significantly enhance the durability of MoS2 as anode materials for Li-ion batteries

  9. Facile synthesis of a MoO2-Mo2C-C composite and its application as favorable anode material for lithium-ion batteries

    Science.gov (United States)

    Zhu, Yanping; Wang, Shaofeng; Zhong, Yijun; Cai, Rui; Li, Li; Shao, Zongping

    2016-03-01

    A composite of MoO2-Mo2C-C is fabricated through a facile ion-exchange route for the first time as an alternative anode material for lithium-ion batteries (LIBs). A macroporous cinnamic anion-exchange resin interacts with ammonium molybdate tetrahydrate in aqueous solution, and the product is then calcined under an inert gas atmosphere. The interaction between the resin and ammonium molybdate tetrahydrate results in an atomic level dispersion of the molybdenum over the organic carbon precursor (resin), while the calcination process allows the formation of MoO2 and Mo2C as well as the pyrolysis of resin to solid carbon. According to field-emission scanning electron microscopy (SEM) and transmission electron microscopy (TEM) measurements, ultrafine MoO2 and Mo2C nanoparticles are uniformly dispersed but firmly attached within an amorphous carbon framework. When evaluated as an anode material, the as-synthesized sample exhibits superior electrochemical performance. The specific discharge capacity is as high as 1491 mA h g-1 in the first cycle and 724 mA h g-1 over 50 cycles at a current density of 0.2 A g-1. This simple, environmentally friendly, low-cost and easily scaled up method, has significant potential for mass industrial production of MoO2-based material as next-generation anode material of LIBs with wide application capability.

  10. Pyrolitic carbon from biomass precursors as anode materials for lithium batteries

    Energy Technology Data Exchange (ETDEWEB)

    Stephan, A. Manuel [School of Chemical Engineering and Technology, Chonbuk National University, Chonju 561-756 (Korea, Republic of); Central Electrochemical Research Institute, Karaikudi 630006 (India); Kumar, T. Prem [Central Electrochemical Research Institute, Karaikudi 630006 (India); Ramesh, R. [Central Electrochemical Research Institute, Karaikudi 630006 (India); Thomas, Sabu [School of Chemical Sciences, Mahatma Gandhi University, Kottayam 686560 (India); Jeong, Soo Kyung [School of Chemical Engineering and Technology, Chonbuk National University, Chonju 561-756 (Korea, Republic of); Nahm, Kee Suk [School of Chemical Engineering and Technology, Chonbuk National University, Chonju 561-756 (Korea, Republic of)]. E-mail: nahmks@chonbuk.ac.kr

    2006-08-25

    Disordered carbonaceous materials were synthesized by the pyrolysis of banana fibers treated with pore-forming substances such as ZnCl{sub 2} and KOH. X-ray diffraction studies indicated a carbon structure with a large number of disorganized single layer carbon sheets. Addition of porogenic agent led to remarkable changes in the structure and morphology of the carbonaceous products. The product obtained with ZnCl{sub 2} treatment gave first-cycle lithium insertion and de-insertion capacities of 3325 and 400 mAh g{sup -1}, respectively. Lower capacities only could be realized in the subsequent cycles, although the coulombic efficiency increased upon cycling, which in the 10th cycle was 95%.

  11. The capacity fading mechanism and improvement of cycling stability in MoS2-based anode materials for lithium-ion batteries.

    Science.gov (United States)

    Shu, Haibo; Li, Feng; Hu, Chenli; Liang, Pei; Cao, Dan; Chen, Xiaoshuang

    2016-02-01

    Two-dimensional (2D) layered MoS2 nanosheets possess great potential as anode materials for lithium ion batteries (LIBs), but they still suffer from poor cycling performance. Improving the cycling stability of electrode materials depends on a deep understanding of their dynamic structural evolution and reaction kinetics in the lithiation process. Herein, thermodynamic phase diagrams and the lithiation dynamics of MoS2-based nanostructures with the intercalation of lithium ions are studied by using first-principles calculations and ab initio molecular dynamics simulations. Our results demonstrate that the continuous intercalation of Li ions induces structural destruction of 2H phase MoS2 nanosheets in the discharge process that follows a layer-by-layer dissociation mechanism. Meanwhile, the intercalation of Li ions leads to a structural transition of MoS2 nanosheets from the 2H to the 1T phase due to the ultralow transition barriers (∼0.1 eV). We find that the phase transition can slow down the dissociation of MoS2 nanosheets during lithiation. The result can be applied to explain extensive experimental observation of the fast capacity fading of MoS2-based anode materials between the first and the subsequent discharges. To suppress the dissociation of MoS2 nanosheets in the lithiation process, we propose a strategy by constructing a sandwich-like graphene/MoS2/graphene structure that indicates high chemical stability, superior conductivity, and high Li-ion mobility in the charge/discharge process, implying the possibility to induce an improvement in the anode cycling performance. This work opens a new route to rational design layered transition-metal disulfide (TMD) anode materials for LIBs with superior cycling stability and electrochemical performance.

  12. Structural and electrochemical studies of a hexaphenylbenzene pyrolysed soft carbon as anode material in lithium batteries

    Energy Technology Data Exchange (ETDEWEB)

    Bonino, Franco; Brutti, Sergio; Piana, Michele; Natale, Sergio; Scrosati, Bruno [Chemistry Department, University ' La Sapienza' , P. le A. Moro 5, 00185 Roma (Italy); Gherghel, Lileta; Muellen, Klaus [Max-Planck Institute for Polymer Research, Ackermannweg 10, 55124 Mainz (Germany)

    2006-04-25

    XRD, SEM micrographs, BET analyses and typical electrochemical experiments (cyclic voltammetry, step voltammetry and Li insertion/deinsertion at constant current) have been carried out to characterize a new type of soft carbons obtained by pyrolysis of hexaphenylbenzene (HPB). By means of XRD and cyclic voltammetry at least three different type of sites for lithium storage were found. The first is graphite like type with d{sub 002} graphene layer distance greater than pure graphite; the second is associated to disordered volumes among crystallites and the third is represented by Li sites at the hydrogen-terminated edges of hexagonal carbon fragments, characterized by higher energy in comparison with simple insertion sites. These last two types of sites are able to store some extra lithium, compared to pure graphite. BET analyses and cyclic voltammetries demonstrate the key role of the milling time on the characteristics and properties of this HPB pyrolysed carbon. Specific capacities shown by this pyrolysed material in Li coin-type cell have been also reported. (author)

  13. In situ X-ray diffraction characterization of NbS2 nanosheets as the anode material for sodium ion batteries

    Science.gov (United States)

    Ou, Xing; Xiong, Xunhui; Zheng, Fenghua; Yang, Chenghao; Lin, Zhihua; Hu, Renzong; Jin, Chao; Chen, Yu; Liu, Meilin

    2016-09-01

    Low cost sodium ion batteries (SIBs) have attracted considerable attentions for large scale electric energy storage (EES), owing to the nature abundance of sodium sources in the earth crust. Searching for appropriate anode materials is a hot topic and vital for developing high performance SIBs. Recently, transition metal dichalcogenides have attracted many interests, as their sandwiched framework stacked up together by van der Waals force can facilitate the electrons transportation and reversible Na+ ions intercalation. Here, NbS2 nanosheets with two-dimensional (2D) layered structure have been fabricated by a facile chemical exfoliation method and been utilized as the anode material for SIBs. The chemically exfoliated NbS2 (ce-NbS2) nanosheets deliver a high reversible specific capacity of 205 mAh g-1 at 100 mA g-1, exhibit high rate performance and excellent cycling stability. In situ X-ray diffraction test demonstrates that ce-NbS2 nanosheets will not suffer any unwanted phase transformation upon soidation/desodiation, which make them promising to construct high capacity and long cycle life anode materials for SIBs.

  14. An in situ method of creating metal oxide–carbon composites and their application as anode materials for lithium-ion batteries

    KAUST Repository

    Yang, Zichao

    2011-01-01

    Transition metal oxides are actively investigated as anode materials for lithium-ion batteries (LIBs), and their nanocomposites with carbon frequently show better performance in galvanostatic cycling studies, compared to the pristine metal oxide. An in situ, scalable method for creating a variety of transition metal oxide-carbon nanocomposites has been developed based on free-radical polymerization and cross-linking of poly(acrylonitrile) in the presence of the metal oxide precursor containing vinyl groups. The approach yields a cross-linked polymer network, which uniformly incorporates nanometre-sized transition metal oxide particles. Thermal treatment of the organic-inorganic hybrid material produces nearly monodisperse metal oxide nanoparticles uniformly embedded in a porous carbon matrix. Cyclic voltammetry and galvanostatic cycling electrochemical measurements in a lithium half-cell are used to evaluate the electrochemical properties of a Fe3O 4-carbon composite created using this approach. These measurements reveal that when used as the anode in a lithium battery, the material exhibits stable cycling performance at both low and high current densities. We further show that the polymer/nanoparticle copolymerization approach can be readily adapted to synthesize metal oxide/carbon nanocomposites based on different particle chemistries for applications in both the anode and cathode of LIBs. © 2011 The Royal Society of Chemistry.

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

    Science.gov (United States)

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

    2015-12-16

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

  16. Anodic oxidation

    CERN Document Server

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

    2013-01-01

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

  17. Discussion on Anode Material for Lithium Ion Battery%对锂离子电池正极材料的探讨与研究

    Institute of Scientific and Technical Information of China (English)

    罗雨晗

    2015-01-01

    Lithium ion battery is currently widely used ,which has the advantage of long life cycle ,no memory effect , high energy density , large specific capacity , high voltage and smaller volume , etc . Lithium ion battery mainly consists of four parts ,including electrolyte ,membrane ,cathode materials and anode materials .Among them ,the cost of anode material occupies a higher proportion in the total cost ,which is about 40% .Each performance index of the lithium ions are related to the quality of anode materials , so anode material is the core part for lithium ion battery ,which is very crucial .At the same time ,the performance of the battery's anode material can also reduce the manufacturing cost of the lithium battery ,which has a great significance for the industrialization of electric vehicles .%锂离子电池目前应用广泛,有循环寿命长、无记忆效应、能量密度大、比容量大、电池电压高、体积较小等优点。锂离子电池主要由电解液、隔膜、负极材料和正极材料四大部分构成,其中,正极材料的成本在总成本中所占有的比例较高,大约为40%,锂离子的各项性能指标均与正极材料的好坏有密切关系,所以,锂离子正极材料是组成锂离子电池的核心部分,是非常关键的材料,同时,电池正极材料的性能也可以使锂电池的制作成本降低,对于电动汽车的产业化也有较大的意义。

  18. Nano-sized Fe{sub 3}O{sub 4}/carbon as anode material for lithium ion battery

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Jie [School of Materials Science and Engineering, University of Science and Technology Beijing, Beijing 100083 (China); Zhao, Hailei, E-mail: hlzhao@ustb.edu.cn [School of Materials Science and Engineering, University of Science and Technology Beijing, Beijing 100083 (China); Beijing Key Lab of New Energy Materials and Technologies, Beijing 100083 (China); Zeng, Zhipeng; Lv, Pengpeng; Li, Zhaolin; Zhang, Tianhou; Yang, Tianrang [School of Materials Science and Engineering, University of Science and Technology Beijing, Beijing 100083 (China)

    2014-12-15

    Nano-sized Fe{sub 3}O{sub 4}/carbon material is prepared via a simple citric-nitrate combustion method combining with a hydrothermal carbon coating technique. The synthesized Fe{sub 3}O{sub 4}/carbon composite shows a high reversible specific capacity (ca. 850 mAh g{sup −1} at 100 mA g{sup −1}; ca. 600 mAh g{sup −1} at 500 mA g{sup −1}), good rate-capability as well as superior cycling stability as anode for lithium-ion batteries. The ameliorated electrochemical performance of Fe{sub 3}O{sub 4}/carbon electrode is associated to the nano-sized particle feature and the continuous carbon coating layer. The former provides short lithium-ion/electron diffusion distance, while the latter enables the fast electron transport pathways. Besides, the carbon layer can act as a protective component to prevent the active particle Fe{sub 3}O{sub 4} from aggregation and pulverization during the charge/discharge processes. - Highlights: • Nano-sized Fe{sub 3}O{sub 4}/C was prepared by a simple citric-nitrate combustion process. • Fe{sub 3}O{sub 4}/C particles show core–shell structure. • Fe{sub 3}O{sub 4}/C powder displays high specific capacity and good cycling stability. • Fe{sub 3}O{sub 4}/C composite exhibits a superior rate-capability.

  19. α-Fe{sub 2}O{sub 3}@C nanorings as anode materials for high performance lithium ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Li, Le; Li, Zhenzhen; Fu, Wenming; Li, Fagen [Department of Physics, Faculty of Science, Ningbo University, Ningbo (China); Wang, Jun, E-mail: wjnaf@ustc.edu [Department of Physics, Faculty of Science, Ningbo University, Ningbo (China); Wang, Wenzhong [School of Science, Minzu University of China, Beijing 100081 (China)

    2015-10-25

    α-Fe{sub 2}O{sub 3}@C core–shell nanorings are prepared by a facile large-scale two-step route incorporating a hydrothermal method and a carbon coated progress. Its structure and morphology are characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscope, and thermogravimetry. It is found that the as-prepared composite is composed of α-Fe{sub 2}O{sub 3}@C nanorings of about 148 nm in outer diameter, 50 nm in thickness, and 115 nm in length. These α-Fe{sub 2}O{sub 3}@C nanorings are enwrapped with ∼3 nm thick carbon shell. And the electrodes exhibit longer cycle life (815 mAhg{sup −1} after cycling 160 times) at high current rate (1000 mAg{sup −1}) compared with that of bare α-Fe{sub 2}O{sub 3} nanorings (810 mAhg{sup −1} after cycling 30 times). The improved performance of the composite is attributed to the bondage from carbon shell, which can enhance the electronic conductivity and structural stability of α-Fe{sub 2}O{sub 3} nanorings. - Highlights: • α-Fe{sub 2}O{sub 3}@C core–shell nanorings are prepared by a facile two-step route. • The α-Fe{sub 2}O{sub 3}@C nanorings are firstly reported as anode materials for LIBs. • The nanorings show a high capacity of 815 mAhg{sup −1} at 1 Ag{sup -1} after 160 cycles.

  20. Defective Ti2Nb10O27.1: an advanced anode material for lithium-ion batteries

    Science.gov (United States)

    Lin, Chunfu; Yu, Shu; Zhao, Hua; Wu, Shunqing; Wang, Guizhen; Yu, Lei; Li, Yanfang; Zhu, Zi-Zhong; Li, Jianbao; Lin, Shiwei

    2015-12-01

    To explore anode materials with large capacities and high rate performances for the lithium-ion batteries of electric vehicles, defective Ti2Nb10O27.1 has been prepared through a facile solid-state reaction in argon. X-ray diffractions combined with Rietveld refinements indicate that Ti2Nb10O27.1 has the same crystal structure with stoichiometric Ti2Nb10O29 (Wadsley-Roth shear structure with A2/m space group) but larger lattice parameters and 6.6% O2- vacancies (vs. all O2- ions). The electronic conductivity and Li+ion diffusion coefficient of Ti2Nb10O27.1 are at least six orders of magnitude and ~2.5 times larger than those of Ti2Nb10O29, respectively. First-principles calculations reveal that the significantly enhanced electronic conductivity is attributed to the formation of impurity bands in Ti2Nb10O29-x and its conductor characteristic. As a result of the improvements in the electronic and ionic conductivities, Ti2Nb10O27.1 exhibits not only a large initial discharge capacity of 329 mAh g-1 and charge capacity of 286 mAh g-1 at 0.1 C but also an outstanding rate performance and cyclability. At 5 C, its charge capacity remains 180 mAh g-1 with large capacity retention of 91.0% after 100 cycles, whereas those of Ti2Nb10O29 are only 90 mAh g-1 and 74.7%.

  1. Processed data from neutron scattering experiments described in PhD thesis "NMR and neutron total scattering studies of silicon-based anode materials for lithium-ion batteries"

    OpenAIRE

    Kerr, Christopher J

    2015-01-01

    The results of processing the data in the dataset "Raw data for neutron scattering experiments described in PhD thesis "NMR and neutron total scattering studies of silicon-based anode materials for lithium-ion batteries""

  2. Mesoporous Silicon-Based Anodes

    Science.gov (United States)

    Peramunage, Dharmasena

    2015-01-01

    For high-capacity, high-performance lithium-ion batteries. A new high-capacity anode composite based on mesoporous silicon is being developed. With a structure that resembles a pseudo one-dimensional phase, the active anode material will accommodate significant volume changes expected upon alloying and dealloying with lithium (Li).

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

    Science.gov (United States)

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

    2015-08-26

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

  4. A first-principles study on the effect of oxygen content on the structural and electronic properties of silicon suboxide as anode material for lithium ion batteries

    Science.gov (United States)

    Rahaman, Obaidur; Mortazavi, Bohayra; Rabczuk, Timon

    2016-03-01

    Silicon suboxide is currently considered as a unique candidate for lithium ion batteries anode materials due to its considerable capacity. However, no adequate information exists about the role of oxygen content on its performance. To this aim, we used density functional theory to create silicon suboxide matrices of various Si:O ratios and investigated the role of oxygen content on the structural, dynamic, electronic properties and lithiation behavior of the matrices. Our study demonstrates that the O atoms interact strongly with the inserted Li atoms resulting in a disintegration of the host matrix. We found that higher concentration of oxygen atoms in the mixture reduces its relative expansion upon lithiation, which is a desirable quality for anode materials. It helps in preventing crack formation and pulverization due to large fluctuations in volume. Our study also demonstrates that a higher oxygen content increases the lithium storage capacity of the anode. However, it can also cause the formation of stable complexes like lithium silicates that might result into reversible capacity loss as indicated by the voltage-composition curves. The study provides valuable insights into the role of oxygen in moderating the interaction of lithium in silicon suboxide mixture in microscopic details.

  5. Facile Sol-Gel/Spray-Drying Synthesis of Interweaved Si@TiO2&CNTs Hybrid Microsphere as Superior Anode Materials for Li-Ion Batteries

    Science.gov (United States)

    Wang, Jiyun; Hou, Xianhua; Li, Yana; Ru, Qiang; Qin, Haiqing; Hu, Shejun

    2016-07-01

    A unique intertwined structure of silicon-based composite (Si@TiO2&CNTs) has been synthesized by sol-gel and spray drying methods. The Si@TiO2&CNTs is mainly composed of three kinds of materials:the prepared nanosilicon particles, TiO2, and carbon nanotubes (CNTs). A layer of TiO2 particles is found effective for enhancing the electrical conductivity and structure stability of the silicon particles. Additionally, the twisted CNTs are beneficial to build a better conductive network, consequently improving the anode working conditions when the cell is charged or discharged. As a lithium ion battery anode, a specific capacity of approximately 1521 mAh g-1 after 100 cycles is obtained.

  6. Surface morphology and surface energy of anode materials influence power outputs in a multi-channel mediatorless bio-photovoltaic (BPV) system.

    Science.gov (United States)

    Bombelli, Paolo; Zarrouati, Marie; Thorne, Rebecca J; Schneider, Kenneth; Rowden, Stephen J L; Ali, Akin; Yunus, Kamran; Cameron, Petra J; Fisher, Adrian C; Ian Wilson, D; Howe, Christopher J; McCormick, Alistair J

    2012-09-21

    Bio-photovoltaic cells (BPVs) are a new photo-bio-electrochemical technology for harnessing solar energy using the photosynthetic activity of autotrophic organisms. Currently power outputs from BPVs are generally low and suffer from low efficiencies. However, a better understanding of the electrochemical interactions between the microbes and conductive materials will be likely to lead to increased power yields. In the current study, the fresh-water, filamentous cyanobacterium Pseudanabaena limnetica (also known as Oscillatoria limnetica) was investigated for exoelectrogenic activity. Biofilms of P. limnetica showed a significant photo response during light-dark cycling in BPVs under mediatorless conditions. A multi-channel BPV device was developed to compare quantitatively the performance of photosynthetic biofilms of this species using a variety of different anodic conductive materials: indium tin oxide-coated polyethylene terephthalate (ITO), stainless steel (SS), glass coated with a conductive polymer (PANI), and carbon paper (CP). Although biofilm growth rates were generally comparable on all materials tested, the amplitude of the photo response and achievable maximum power outputs were significantly different. ITO and SS demonstrated the largest photo responses, whereas CP showed the lowest power outputs under both light and dark conditions. Furthermore, differences in the ratios of light : dark power outputs indicated that the electrochemical interactions between photosynthetic microbes and the anode may differ under light and dark conditions depending on the anodic material used. Comparisons between BPV performances and material characteristics revealed that surface roughness and surface energy, particularly the ratio of non-polar to polar interactions (the CQ ratio), may be more important than available surface area in determining biocompatibility and maximum power outputs in microbial electrochemical systems. Notably, CP was readily outperformed by all

  7. The Progress of Sodium-Ion Battery Anode Material%钠离子电池负极材料的研究进展

    Institute of Scientific and Technical Information of China (English)

    张洁; 杨占旭

    2016-01-01

    Sodium ion batteries have attracted tremendous attentions due to its rich resources,low cost,high efficiency and good chemical stability,and can satisfy people's demand for energy in the new era,which are considered a top alternative to lithium-ion batteries.The research progress on sodium ion battery anode materials are reviewed in details in this paper, including carbon-based materials,low voltage metal phosphates,the sodium storage alloys,metal oxides,titanium-based materials,and other negative electrode materials.Then the characteristics of anode materials are discussed.Finally,some future directions for sodium-ion battery anode materials are pointed out.%钠离子电池具有资源丰富、成本低、效率高、化学性能稳定等优点,成为锂离子电池 的理想替代品.主要阐述了钠离子电池负极材料的研究进展,包括碳基负极材料、低电压金属磷酸盐负极材料、合金类储钠负极材料、金属氧化物负极材料、钛酸盐类负极材料及其他负极材料,并对各类负极材料的性能进行了评价,最后对钠离子电池负极材料的发展方向做出了展望.

  8. Novel silicon and tin alloy nano-particulate materials via spark erosion for high performance and high capacity anodes in lithium ion batteries

    Science.gov (United States)

    White, Emma Marie Hamilton

    The advent and popularity of portable electronics, as well as the need to reduce carbon-based fuel dependence for environmental and economic reasons, has led to the search for higher energy density portable power storage methods. Lithium ion batteries offer the highest energy density of any portable energy storage technology, but their potential is limited by the currently used materials. Theoretical capacities of silicon (3580 mAh/g) and tin (990 mAh/g) are significantly higher than existing graphitic anodes (372 mAh/g). However, silicon and tin must be scaled down to the nano-level to mitigate the pulverization from drastic volume changes in the anode structure during lithium ion insertion/extraction. The available synthesis techniques for silicon and tin nano-particles are complicated and scale-up is costly. A unique one-step process for synthesizing Si-Sn alloy and Sn nano-particles via spark plasma erosion has been developed to achieve the ideal nano-particulate size and carbon coating architecture. Spark erosion produces crystalline and amorphous spherical nano-particles, averaging 5-500nm in diameter. Several tin and silicon alloys have been spark eroded and thoroughly characterized using SEM, TEM, EDS, XPS, Auger spectroscopy, NMR spectroscopy and TGA. The resulting nano-particles show improved performance as anodes over commercialized materials. In particular, pure sparked Sn particles show stable reversible capacity at ˜460 mAh/g with >99.5% coulombic efficiency for over 100 cycles. These particles are drop-in ready for existing commercial anode processing techniques and by only adding 10% of the sparked Sn particles the total current cell capacity will increase by ˜13%.

  9. Multi-walled carbon nanotube-reinforced porous iron oxide as a superior anode material for lithium ion battery

    Energy Technology Data Exchange (ETDEWEB)

    Pang, Xin-Jing; Zhang, Juan; Qi, Gong-Wei; Dai, Xiao-Hui; Zhou, Jun-Ping [School of Chemistry and Chemical Engineering, Shandong University, No. 27, Shanda Nan Rd., Jinan 250100 (China); Zhang, Shu-Yong, E-mail: syzhang@sdu.edu.cn [School of Chemistry and Chemical Engineering, Shandong University, No. 27, Shanda Nan Rd., Jinan 250100 (China); National Key Lab of Crystal, Shandong University, No. 27, Shanda Nan Rd., Jinan 250100 (China)

    2015-08-15

    Highlights: • Electrochemical performance of Fe{sub 3}O{sub 4} is improved by combining different approaches. • Porous Cu substrate is used to enlarge surface area and improve conductivity. • MWCNT is used to reinforce the electrode structure and change morphology of Fe{sub 3}O{sub 4}. • Reversible capacity, capacity retention and high-rate performance are improved. - Abstract: Multi-walled carbon nanotube-reinforced porous iron oxide (Fe{sub 3}O{sub 4}/MWCNT) is synthesized by a two-step approach with porous Cu substrate serving as current collector. Porous Cu substrate is prepared through electroless deposition with hydrogen bubble serving as template. Fe{sub 3}O{sub 4}/MWCNT composites are prepared by the electrodeposition of Fe{sub 3}O{sub 4} in the presence of dispersed MWCNTs from a Fe{sub 2}(SO{sub 4}){sub 3} solution with MWCNT suspension. Results showed that Fe{sub 3}O{sub 4} forms granular nanoparticles on the porous Cu substrate with several MWCNTs embedded in it. Adding MWCNTs changes the morphology of Fe{sub 3}O{sub 4}. Smooth Fe{sub 3}O{sub 4}, smooth Fe{sub 3}O{sub 4}/MWCNT, and porous Fe{sub 3}O{sub 4} composites are also prepared for comparison. When used as anode materials, porous Fe{sub 3}O{sub 4}/MWCNT composites have a reversible capacity of approximately 601 mA h g{sup −1} at the 60th cycle at a cycling rate of 100 mA g{sup −1}. This value is higher than that of the other materials. The reversible capacity at a cycling rate of 10,000 mA g{sup −1} is approximately 50% of that at 100 mA g{sup −1}. Therefore, the MWCNT-reinforced porous Fe{sub 3}O{sub 4} composite exhibits much better reversible capacity, capacity retention, and high-rate performance than the other samples. This finding can be ascribed to the porous structure of Fe{sub 3}O{sub 4}, better conductivity of porous Cu substrate and MWCNTs, and the morphology change of Fe{sub 3}O{sub 4} nanoparticles upon the addition of MWCNTs.

  10. SnO2 nanocrystals deposited on multiwalled carbon nanotubes with superior stability as anode material for Li-ion batteries

    Science.gov (United States)

    Ren, Jianguo; Yang, Junbing; Abouimrane, Ali; Wang, Dapeng; Amine, Khalil

    2011-10-01

    We report a novel ethylene glycol-mediated solvothermal-polyol route for synthesis of SnO2-CNT nanocomposites, which consist of highly dispersed 3-5 nm SnO2 nanocrystals on the surface of multiwalled carbon nanotubes (CNTs). As anode materials for Li-ion batteries, the nanocomposites showed high rate capability and superior cycling stability with specific capacity of 500 mAh g-1 for up to 300 cycles. The CNTs served as electron conductors and volume buffers in the nanocomposites. This strategy could be extended to synthesize other metal oxides composites with other carbon materials.

  11. Preparation and electrochemical properties of core-shell carbon coated Mn–Sn complex metal oxide as anode materials for lithium-ion batteries

    International Nuclear Information System (INIS)

    In this study, we synthesized a carbon coated Mn–Sn metal oxide composite with core-shell structure (MTO@C) via a simple glucose hydrothermal reaction and subsequent carbonization approach. When the MTO@C composite was applied as an anode material for lithium-ion batteries, it maintained a reversible capacity of 409 mA h g−1 after 200 cycles at a current density of 100 mA g−1. The uniformed and continuous carbon layer formed on the MTO nanoparticles, effectively buffered the volumetric change of the active material and increased electronic conductivity, which thus prolonged the cycling performance of the MTO@C electrode.

  12. Ultrafast synthesis of MoS2 or WS2-reduced graphene oxide composites via hybrid microwave annealing for anode materials of lithium ion batteries

    Science.gov (United States)

    Youn, Duck Hyun; Jo, Changshin; Kim, Jae Young; Lee, Jinwoo; Lee, Jae Sung

    2015-11-01

    An ultrafast and simple strategy to synthesize metal sulfides (MoS2 and WS2) anchored on reduced graphene oxide (RGO) composites is reported as anode materials for lithium ion batteries (LIBs). Metal sulfide nanocrystals with homogeneous dispersion onto conducting RGO sheets are obtained in only 45 s by hybrid microwave annealing (HMA) method. The synthesized materials, especially MoS2/RGO composite, exhibit a high Li capacity, an excellent rate capability, and a stable cycling performance, comparable to the reported best MS2/carbon composite electrodes. The results highlight the effectiveness of HMA method to fabricate the metal sulfide/RGO composites with excellent electric properties.

  13. Nano-sized Li4Ti5O12 anode material with excellent performance prepared by solid state reaction: The effect of precursor size and morphology

    International Nuclear Information System (INIS)

    Graphical abstract: - Highlights: • Nano-sized Li4Ti5O12 has been prepared through solid state reaction by using axiolitic TiO2 as precursor. • The prepared nano-sized Li4Ti5O12 anode material shows excellent electrochemical performance. • The utilization of precursor with special morphology and size is one of the useful ways to prepare more active electrode materials. - Abstract: Spinel nano-sized Li4Ti5O12 anode material of secondary lithium-ion battery has been successfully prepared by solid state reaction using axiolitic TiO2 assembled by 10–20 nm nanoparticles and Li2CO3 as precursors. The synthesis condition, grain size effect and corresponding electrochemical performance of the special Li4Ti5O12 have been studied in comparison with those of the normal Li4Ti5O12 originated from commercial TiO2. We also propose the mechanism that using the nano-scaled TiO2 with special structure and unexcess Li2CO3 as precursors can synthesize pure phase nano-sized Li4Ti5O12 at 800 °C through solid state reaction. The prepared nano-sized Li4Ti5O12 anode material for Li-ion batteries shows excellent capacity performance with rate capacity of 174.2, 164.0, 157.4, 146.4 and 129.6 mA h g−1 at 0.5, 1, 2, 5 and 10 C, respectively, and capacity retention of 95.1% after 100 cycles at 1 C. In addition, the specific capacity fade for the cell with the different Li4Ti5O12 active materials resulted from the increase of internal resistance after 100 cycles is compared

  14. TiNb2O7/Graphene hybrid material as high performance anode for lithium-ion batteries

    International Nuclear Information System (INIS)

    We report the synthesis of TiNb2O7/Graphene (TNO-TG) hybrid nanomaterial by simple solvothermal process, with TiNb2O7 nanoparticles anchored on the reduced graphene oxide (rGO) sheets. TNO-TG hybrid nanomaterial showed excellent electrochemical performance when studied as anode for Lithium-ion battery, with an exceptionally high rate capability (capacity retention of 80% at 16 C rate) along with high discharge capacity (∼230 mAhg−1 after 50 cycles at 0.1 C). A full cell Li-ion battery has been fabricated with TNO-TG as anode and LiNi1/3Mn1/3Co1/3O2:LiNi0.5Mn0.5O2 (wt% of 75:25) as cathode, which delivered an average cell voltage of ∼2.5 V with an initial anode-specific discharge capacity of 211 mAhg−1, when cycled in the voltage range of 1.5–3.5 V at 0.1 C. The obtained results are very promising and we believe the current findings will lead to new directions in the on-going search for safe and high performance anodes for rechargeable lithium-ion batteries

  15. Multiwalled carbon nanotube@a-C@Co9S8 nanocomposites: a high-capacity and long-life anode material for advanced lithium ion batteries

    Science.gov (United States)

    Zhou, Yanli; Yan, Dong; Xu, Huayun; Liu, Shuo; Yang, Jian; Qian, Yitai

    2015-02-01

    A one-dimensional MWCNT@a-C@Co9S8 nanocomposite has been prepared via a facile solvothermal reaction followed by a calcination process. The amorphous carbon layer between Co9S8 and MWCNT acts as a linker to increase the loading of sulfides on MWCNT. When evaluated as anode materials for lithium ion batteries, the MWCNT@a-C@Co9S8 nanocomposite shows the advantages of high capacity and long life, superior to Co9S8 nanoparticles and MWCNT@Co9S8 nanocomposites. The reversible capacity could be retained at 662 mA h g-1 after 120 cycles at 1 A g-1. The efficient synthesis and excellent performances of this nanocomposite offer numerous opportunities for other sulfides as a new anode for lithium ion batteries.A one-dimensional MWCNT@a-C@Co9S8 nanocomposite has been prepared via a facile solvothermal reaction followed by a calcination process. The amorphous carbon layer between Co9S8 and MWCNT acts as a linker to increase the loading of sulfides on MWCNT. When evaluated as anode materials for lithium ion batteries, the MWCNT@a-C@Co9S8 nanocomposite shows the advantages of high capacity and long life, superior to Co9S8 nanoparticles and MWCNT@Co9S8 nanocomposites. The reversible capacity could be retained at 662 mA h g-1 after 120 cycles at 1 A g-1. The efficient synthesis and excellent performances of this nanocomposite offer numerous opportunities for other sulfides as a new anode for lithium ion batteries. Electronic supplementary information (ESI) available: Infrared spectrogram (IR) of glucose treated MWCNT; TEM images of MWCNT@a-C treated by different concentrations of glucose; SEM and TEM images of the intermediate product obtained from the solvothermal reaction between thiourea and Co(Ac)2; EDS spectrum of MWCNT@a-C@Co9S8 composites; SEM and TEM images of MWCNT@Co9S8 nanocomposites obtained without the hydrothermal treatment by glucose; SEM and TEM images of Co9S8 nanoparticles; Galvanostatic discharge-charge profiles and cycling performance of MWCNT@a-C; TEM images

  16. FeS anchored reduced graphene oxide nanosheets as advanced anode material with superior high-rate performance for alkaline secondary batteries

    Science.gov (United States)

    Shangguan, Enbo; Guo, Litan; Li, Fei; Wang, Qin; Li, Jing; Li, Quanmin; Chang, Zhaorong; Yuan, Xiao-Zi

    2016-09-01

    A new nanocomposite formulation of the iron-based anode for alkaline secondary batteries is proposed. For the first time, FeS nanoparticles anchored on reduced graphene oxide (RGO) nanosheets are synthesized via a facile, environmentally friendly direct-precipitation approach. In this nanocomposite, FeS nanoparticles are anchored uniformly and tightly on the surface of RGO nanosheets. As an alkaline battery anode, the FeS@RGO electrode delivers a superior high-rate charge/discharge capability and outstanding cycling stability, even at a condition without any conductive additives and a high electrode loading of ∼40 mg cm-2. At high charge/discharge rates of 5C, 10C and 20C (6000 mA g-1), the FeS@RGO electrode presents a specific capacity of ∼288, 258 and 220 mAh g-1, respectively. Moreover, the FeS@RGO electrode exhibits an admirable long cycling stability with a superior capacity retention of 87.6% for 300 cycles at a charge/discharge rate of 2C. The excellent electrochemical properties of the FeS@RGO electrode can be stemmed from the high specific surface area, peculiar electric conductivity and robust sheet-anchored structure of the FeS@RGO nanocomposite. By virtue of its superior fast charge/discharge properties, the FeS@RGO nanocomposite is suitable as an advanced anode material for high-performance alkaline secondary batteries.

  17. Green synthesis of mesoporous ZnFe2O4/C composite microspheres as superior anode materials for lithium-ion batteries

    Science.gov (United States)

    Yao, Lingmin; Hou, Xianhua; Hu, Shejun; Wang, Jie; Li, Min; Su, Chao; Tade, Moses O.; Shao, Zongping; Liu, Xiang

    2014-07-01

    The commercialized LIBs employing graphite as anodes currently suffer a series of problems from the safety, theoretical capacity (372 mAh g-1) and rate capability. Herein, self-assembly mesoporous Zn ferrite (ZnFe2O4) microsphere embedded into carbon network has been synthesized by a facile method in the presence of citric acid. The Zn ferrites as an anode material with novel structure demonstrate superior electrochemical performance, with enhanced specific reversible capacity (∼1100 mAh g-1 at the specific current of 0.05 A g-1 after 100 cycles), excellent rate capability (more than 500 mAh g-1 even at the specific current of 1.1 A g-1) and good cycleability with little fading (∼97.6% after 100 cycles). The excellent cycling performance is associated with the loose Zn ferrite microsphere with numerous mesopores embedded into the carbon network, which can accommodate the severe mechanism strains and provides good electrical contact and conductivity. The superior electrochemical performance may facilitate ZnFe2O4 to be a promising alternative anode in lithium ion battery.

  18. Synthesis of nickel oxide nanospheres by a facile spray drying method and their application as anode materials for lithium ion batteries

    Energy Technology Data Exchange (ETDEWEB)

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

    2015-10-15

    Graphical abstract: NiO nanospheres prepared by a facile spray drying method show high lithium ion storage performance as anode of lithium ion battery. - Highlights: • NiO nanospheres are prepared by a spray drying method. • NiO nanospheres are composed of interconnected nanoparticles. • NiO nanospheres show good lithium ion storage properties. - Abstract: Fabrication of advanced anode materials is indispensable for construction of high-performance lithium ion batteries. In this work, nickel oxide (NiO) nanospheres are fabricated by a facial one-step spray drying method. The as-prepared NiO nanospheres show diameters ranging from 100 to 600 nm and are composed of nanoparticles of 30–50 nm. As an anode for lithium ion batteries, the electrochemical properties of the NiO nanospheres are investigated by cyclic voltammetry (CV) and galvanostatic charge/discharge tests. The specific reversible capacity of NiO nanospheres is 656 mA h g{sup −1} at 0.1 C, and 476 mA h g{sup −1} at 1 C. The improvement of electrochemical properties is attributed to nanosphere structure with large surface area and short ion/electron transfer path.

  19. 锂离子电池硅基负极材料研究进展%Research Progress of Silicon Based Anode Materials for Lithium-ion Batteries

    Institute of Scientific and Technical Information of China (English)

    杨绍斌; 刘远鹏

    2011-01-01

    Silicon based materials are candidate anode materials for lithium-ion battery because of its large spe cific capacity. But the decay of capacity during cycling restrains the practicability of silicon-based material. Two im portant research aspects of silicon-based materials are reviewed, including the silicon compounds powder and silicon thin film, and a single modification approach cannot satisfy the practical application is pointed out So, the comprehen sive use of nanocrystallization, amorphization and alloying becomes the main approach in silicon, based anode mate rials.%硅基负极材料具有比容量大的优点,是高容量锂离子电池理想的负极材料.然而硅基材料在循环过程中容量衰减快,影响了其实用性.从硅复合物粉末和硅薄膜两个重要研究方面对硅基负极材料进行了综述,指出在Si基复合负极材料的研究中,单一途径改性提升循环性能的幅度有限,很难达到实用化阶段.硅的纳米化、无定形化、合金化及复合化等方法的综合运用成为硅基材料研究的主导方向.

  20. Enhanced cycle stability of micro-sized Si/C anode material with low carbon content fabricated via spray drying and in situ carbonization

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Dingsheng; Gao, Mingxia, E-mail: gaomx@zju.edu.cn; Pan, Hongge; Liu, Yongfeng; Wang, Junhua; Li, Shouquan; Ge, Hongwei

    2014-08-01

    Highlights: • Micro-sized Si/C composites were fabricated via. spray drying and carbonization. • Multi-morphology carbon was formed in the Si/C composites. • Si/C composite with 5.6 wt.% C provides significant improved cycling stability. • Multi-morphology carbon plays effective role in improving the electrochemical property. • The method provides potential for mass production of superior Si-based anode materials. - Abstract: Micro-sized Si/C composites with in situ introduced carbon of multi-morphology were fabricated via spray drying a suspension of commercial micro-sized Si and citric acid followed by a carbonization. Different ratios of Si to citric acid were used to optimize the composition and structure of the composites and thus the electrochemical performance. Carbon flakes including crooked and flat ones were well dispersed in between the Si particles, forming Si/C composites. Floc-like carbon layers and carbon fragments were also found to cover partially the Si particles. The Si/C composite with a low carbon content of 5.6 wt.% provides an initial reversible capacity of 2700 mA h/g and a capacity of 1860 mA h/g after 60 cycles at a current density of 100 mA/g as anode material for lithium-ion batteries (LIBs), which are much higher than those of pristine Si and the Si/C composites with higher carbon content. The mechanism of the enhancement of electrochemical performance of the micro-sized Si/C composite is discussed. The fabrication method and the structure design of the composites offer valuable potential in developing adaptable Si-based anode materials for industrial applications.

  1. Anode sheath transition in an anodic arc for synthesis of nanomaterials

    Science.gov (United States)

    Nemchinsky, V. A.; Raitses, Y.

    2016-06-01

    The arc discharge with ablating anode or so-called anodic arc is widely used for synthesis of nanomaterials, including carbon nanotubes and fullerens, metal nanoparticles etc. We present the model of this arc, which confirms the existence of the two different modes of the arc operation with two different anode sheath regimes, namely, with negative anode sheath and with positive anode sheath. It was previously suggested that these regimes are associated with two different anode ablating modes—low ablation mode with constant ablation rate and the enhanced ablation mode (Fetterman et al 2008 Carbon 46 1322). The transition of the arc operation from low ablation mode to high ablation mode is determined by the current density at the anode. The model can be used to self-consistently determine the distribution of the electric field, electron density and electron temperature in the near-anode region of the arc discharge. Simulations of the carbon arc predict that for low arc ablating modes, the current is driven mainly by the electron diffusion to the anode. For positive anode sheath, the anode voltage is close to the ionization potential of anode material, while for negative anode sheath, the anode voltage is an order of magnitude smaller. It is also shown that the near-anode plasma, is far from the ionization equilibrium.

  2. N-doped graphene/graphite composite as a conductive agent-free anode material for lithium ion batteries with greatly enhanced electrochemical performance

    International Nuclear Information System (INIS)

    Graphical abstract: The study reported a novel N-doped graphene/graphite anode material for lithium ion batteries. The composite exhibits a largely enhanced electrochemical performance. The study also provides an attractive approach for the fabrication of various graphite-based materials for high power batteries. Display Omitted -- Highlights: • The paper developed a new N-doped graphene/graphite composite for lithium ion battery • The composite contains a three-dimensional graphene framework with rich of open pores • The hybrid offers a higher electrical conductivity when compared with pristine graphite • The hybrid electrode provides a greatly enhanced electrochemical performance • The study provides a prominent approach for fabrication of graphite-based materials -- ABSTRACT: Present graphite anode cannot meet the increasing requirement of electronic devices and electric vehicles due to its low specific capacity, poor cycle stability and low rate capability. The study reported a promising N-doped graphene/graphite composite as a conductive agent-free anode material for lithium ion batteries. Herein, graphite oxide and urea were dispersed in ultrapure water and partly reduced by ascorbic acid. Followed by mixing with graphite and hydrothermal treatment to produce graphene oxide/graphite hydrogel. The hydrogel was dried and finally annealed in Ar/H2 to obtain N-doped graphene/graphite composite. The result shows that all of graphite particles was dispersed in three-dimensional graphene framework with a rich of open pores. The open pore accelerates the electrolyte transport. The graphene framework works as a conductive agent and graphite particle connector and improves the electron transfer. Electrical conductivity of the composite reaches 5912 S m−1, which is much better than that of the pristine graphite (4018 S m−1). The graphene framework also acts as an expansion absorber in the anodes of lithium ion battery to relieve the large strains developed

  3. Leaching lithium from the anode electrode materials of spent lithium-ion batteries by hydrochloric acid (HCl).

    Science.gov (United States)

    Guo, Yang; Li, Feng; Zhu, Haochen; Li, Guangming; Huang, Juwen; He, Wenzhi

    2016-05-01

    Spent lithium-ion batteries (LIBs) are considered as an important secondary resource for its high contents of valuable components, such as lithium and cobalt. Currently, studies mainly focus on the recycling of cathode electrodes. There are few studies concentrating on the recovery of anode electrodes. In this work, based on the analysis result of high amount of lithium contained in the anode electrode, the acid leaching process was applied to recycle lithium from anode electrodes of spent LIBs. Hydrochloric acid was introduced as leaching reagent, and hydrogen peroxide as reducing agent. Within the range of experiment performed, hydrogen peroxide was found to have little effect on lithium leaching process. The highest leaching recovery of 99.4wt% Li was obtained at leaching temperature of 80°C, 3M hydrochloric acid and S/L ratio of 1:50g/ml for 90min. The graphite configuration with a better crystal structure obtained after the leaching process can also be recycled.

  4. Enhanced rate performance of nanosized Li4Ti5O12/graphene composites as anode material by a solid state-assembly method

    International Nuclear Information System (INIS)

    Highlights: • Nanosized Li4Ti5O12/graphene material synthesized by a solid state-assembly method is first reported. • Li4Ti5O12/graphene materials exhibit high specific capacity and cycle stability. • Li4Ti5O12/graphene anodes remarkably exhibit high rate performance. • Li4Ti5O12/graphene improves the conductivity. -- Abstract: Nanosized Li4Ti5O12/graphene materials have been successfully synthesized by a solid state-assembly method. As the anode materials for lithium ion batteries, nanosized Li4Ti5O12/graphene exhibits higher specific capacity, much improved rate capability, and better cycle stability than the pure Li4Ti5O12. In the potential range of 1.0-2.0 V at room temperature, Li4Ti5O12/graphene with weight ratio of LTO:GO to 1000:5 shows discharge capacities of more than 144 and 96.2 mAh g−1 after 100 cycles at 1C and 3C charge-discharge rates, while the correspond discharge capacities of pure Li4Ti5O12 are only 108 and 75.4 mAh g−1, respectively. The resulting Li4Ti5O15/graphene (1000:5) sample demonstrates remarkable rate capability in that it delivers a reversible capacity of 53.4 mAh g−1 in the 1000th cycle at 10C charge-discharge rate, about 240% that of pristine Li4Ti5O12 particles (22.2 mAh g−1). The low charge-transfer resistance and large lithium ion diffusion coefficients confirmed that Li4Ti5O12/graphene materials possessed better electronic conductivity and lithium ion mobility. The present work demonstrates that Li4Ti5O12/graphene composite is a promising anode material for high-rate and long life lithium ion batteries and this simple preparation method makes its production on a large scale

  5. A novel nano-structured interpenetrating phase composite of silicon/graphite–tin for lithium-ion rechargeable batteries anode materials

    International Nuclear Information System (INIS)

    Highlights: • An interpenetrating phase composite is synthesized by high energy mechanical milling. • Silicon and tin interpenetrate into each other in the composite. • The SGM composite shows good electrochemical properties. • The lithiation and delithiation reaction mechanism are investigated. - Abstract: A novel nano-structured interpenetrating phase composite (NSIPC) of silicon/graphite–tin (SGM) anode material for lithium-ion rechargeable batteries is synthesized by high energy mechanical milling (HEMM). The structural and morphological characterizations have been carried out through X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The electrochemical performances have been analyzed with reference to Li+/Li and the results are compared with silicon/graphite composites. The SGM NSIPC electrode exhibits the better cyclability than the SG composite electrodes. The initial discharge specific capacity of the as-prepared SGM NSIPC is relatively high around 1790 mA h g−1 with 1592 mA h g−1 reversible capacity retention in the following cycle at a current density of 237 mA g−1 in the voltage from 0.03 V to 1.5 V. In addition, the SGM NSIPC electrode shows the good rate capability and possesses the stable cycling performance even charging and discharging at the large current density. Consequently, SGM NSIPC can be the promising anode material for the next generation lithium ion rechargeable batteries

  6. PbLi2Ti6O14: A novel high-rate long-life anode material for rechargeable lithium-ion batteries

    Science.gov (United States)

    Li, Peng; Qian, Shangshu; Yu, Haoxiang; Yan, Lei; Lin, Xiaoting; Yang, Ke; Long, Nengbing; Shui, Miao; Shu, Jie

    2016-10-01

    As a novel anode material, PbLi2Ti6O14 is prepared by a traditional solid state method at a calcination temperature of 900 °C. Structural analysis and electrochemical tests prove that PbLi2Ti6O14 possesses a good crystallinity and superior performance. PbLi2Ti6O14, composed of particles with 400 nm in length and 300 nm in width, exhibits an initial charge capacity of 155.1 mAh g-1 at 100 mA g-1 and maintains at 147.9 mAh g-1 after 100 cycles, with capacity retention as high as 95.4%. Especially, the reversible capacity of PbLi2Ti6O14 can stabilize at 101.6 mAh g-1 after 1000 cycles at a high current density of 1000 mA g-1, with capacity retention of 87.5%. Besides, the lithium storage behavior in PbLi2Ti6O14 is also studied by various in-situ and ex-situ methods. It is found that the lithiation/delithiation process in PbLi2Ti6O14 is a highly reversible reaction. All these results demonstrate that PbLi2Ti6O14 may be an impressive anode material in the near future.

  7. Flake-by-flake ZnCo2O4 as a high capacity anode material for lithium-ion battery

    International Nuclear Information System (INIS)

    Highlights: • The ZnCo2O4 with porous structure was prepared by co-precipitation method. • Flake-by-flake used in ZnCo2O4 was studied for the first time. • The as-prepared ZCO shows excellent electrochemical performances. • The preparation method has mild experiment conditions and high production rate. -- Abstract: A novel flake-by-flake ZnCo2O4 (ZCO) with porous nanostructure is prepared by a typical and facile co-precipitation method using oxalic acid as complex agent. XRD, SEM, and TEM analyses show the as-prepared ZCO nanoparticles have a high purity and a good crystallinity, and the ZCO nanoflakes with a thickness of 30–80 nm are composed of uniform ZCO nanocrystals with a diameter of 20–40 nm. The novel structure with enough free space is beneficial to improving the electrochemical performance. The as-prepared ZCO used as an anode material for lithium-ion batteries exhibits a high specific capacity of 1275 mA h/g at a current rate of 100 mA/g after 50 cycles, as well as a high power capability at elevated current rates, i.e., 1130 and 730 mA h/g at current rates of 500 and 3000 mA/g, respectively. It has a great prospect for the application of anode materials for lithium-ion batteries

  8. Interfacial effect on the electrochemical properties of the layered graphene/metal sulfide composites as anode materials for Li-ion batteries

    Science.gov (United States)

    Lv, Yagang; Chen, Biao; Zhao, Naiqin; Shi, Chunsheng; He, Chunnian; Li, Jiajun; Liu, Enzuo

    2016-09-01

    The layered graphene/metal sulfide composites exhibit excellent electrochemical properties as anode materials for lithium ion battery, due to the synergistic effect between metal sulfide and graphene which still needs to be further understood. In this study, Li adsorption and diffusion on MoS2 and SnS2 monolayers and Li2S surface, as well as at their interfaces with graphene, are systematically investigated through first-principles calculations. The analysis of charge density difference, Bader charge, and density of states indicates that the adsorbed Li atoms interact with both the S atoms at metal sulfide surfaces and C atoms in graphene, resulting in larger Li adsorption energies at the interfaces compared with that on the corresponding surfaces, but with almost no enhancement of the energy barriers for Li atom diffusion. The enhanced Li adsorption capability at Li2S/G interface contributes to the extra storage capacity of graphene/metal sulfide composites. Furthermore, the synergistic mechanism between metal sulfide and graphene is revealed. Moreover, band structure analysis shows the electronic conductivity is enhanced with the incorporation of graphene. The results corroborate the interfacial pseudocapacity-like Li atom storage mechanism, and are helpful for the design of layered graphene/metal sulfide composites as anode materials for lithium ion batteries.

  9. Integrating 3D Flower-Like Hierarchical Cu2NiSnS4 with Reduced Graphene Oxide as Advanced Anode Materials for Na-Ion Batteries.

    Science.gov (United States)

    Yuan, Shuang; Wang, Sai; Li, Lin; Zhu, Yun-hai; Zhang, Xin-bo; Yan, Jun-min

    2016-04-13

    Development of an anode material with high performance and low cost is crucial for implementation of next-generation Na-ion batteries (NIBs) electrode, which is proposed to meet the challenges of large scale renewable energy storage. Metal chalcogenides are considered as promising anode materials for NIBs due to their high theoretical capacity, low cost, and abundant sources. Unfortunately, their practical application in NIBs is still hindered because of low conductivity and morphological collapse caused by their volume expansion and shrinkage during Na(+) intercalation/deintercalation. To solve the daunting challenges, herein, we fabricated novel three-dimensional (3D) Cu2NiSnS4 nanoflowers (CNTSNs) as a proof-of-concept experiment using a facile and low-cost method. Furthermore, homogeneous integration with reduced graphene oxide nanosheets (RGNs) endows intrinsically insulated CNTSNs with superior electrochemical performances, including high specific capacity (up to 837 mAh g(-1)), good rate capability, and long cycling stability, which could be attributed to the unique 3D hierarchical structure providing fast ion diffusion pathway and high contact area at the electrode/electrolyte interface. PMID:26986821

  10. Flake-by-flake ZnCo{sub 2}O{sub 4} as a high capacity anode material for lithium-ion battery

    Energy Technology Data Exchange (ETDEWEB)

    Song, Xiong [School of Physics and Telecommunication Engineering, South China Normal University, Guangzhou 510006 (China); Engineering Research Center of Materials and Technology for Electrochemical Energy Storage (Ministry of Education), Guangzhou 510006 (China); Ru, Qiang, E-mail: rq7702@yeah.net [School of Physics and Telecommunication Engineering, South China Normal University, Guangzhou 510006 (China); Engineering Research Center of Materials and Technology for Electrochemical Energy Storage (Ministry of Education), Guangzhou 510006 (China); Laboratory of Quantum Information Technology, School of Physics and Telecommunication Engineering, South China Normal University, Guangzhou 510006 (China); Zhang, Beibei; Hu, Shejun; An, Bonan [School of Physics and Telecommunication Engineering, South China Normal University, Guangzhou 510006 (China); Engineering Research Center of Materials and Technology for Electrochemical Energy Storage (Ministry of Education), Guangzhou 510006 (China)

    2014-02-05

    Highlights: • The ZnCo{sub 2}O{sub 4} with porous structure was prepared by co-precipitation method. • Flake-by-flake used in ZnCo{sub 2}O{sub 4} was studied for the first time. • The as-prepared ZCO shows excellent electrochemical performances. • The preparation method has mild experiment conditions and high production rate. -- Abstract: A novel flake-by-flake ZnCo{sub 2}O{sub 4} (ZCO) with porous nanostructure is prepared by a typical and facile co-precipitation method using oxalic acid as complex agent. XRD, SEM, and TEM analyses show the as-prepared ZCO nanoparticles have a high purity and a good crystallinity, and the ZCO nanoflakes with a thickness of 30–80 nm are composed of uniform ZCO nanocrystals with a diameter of 20–40 nm. The novel structure with enough free space is beneficial to improving the electrochemical performance. The as-prepared ZCO used as an anode material for lithium-ion batteries exhibits a high specific capacity of 1275 mA h/g at a current rate of 100 mA/g after 50 cycles, as well as a high power capability at elevated current rates, i.e., 1130 and 730 mA h/g at current rates of 500 and 3000 mA/g, respectively. It has a great prospect for the application of anode materials for lithium-ion batteries.

  11. Hierarchical MoS2 tubular structures internally wired by carbon nanotubes as a highly stable anode material for lithium-ion batteries

    Science.gov (United States)

    Chen, Yu Ming; Yu, Xin Yao; Li, Zhen; Paik, Ungyu; Lou, Xiong Wen (David)

    2016-01-01

    Molybdenum disulfide (MoS2), a typical two-dimensional material, is a promising anode material for lithium-ion batteries because it has three times the theoretical capacity of graphite. The main challenges associated with MoS2 anodes are the structural degradation and the low rate capability caused by the low intrinsic electric conductivity and large strain upon cycling. Here, we design hierarchical MoS2 tubular structures internally wired by carbon nanotubes (CNTs) to tackle these problems. These porous MoS2 tubular structures are constructed from building blocks of ultrathin nanosheets, which are believed to benefit the electrochemical reactions. Benefiting from the unique structural and compositional characteristics, these CNT-wired MoS2 tubular structures deliver a very high specific capacity of ~1320 mAh g−1 at a current density of 0.1 A g−1, exceptional rate capability, and an ultralong cycle life of up to 1000 cycles. This work may inspire new ideas for constructing high-performance electrodes for electrochemical energy storage. PMID:27453938

  12. The capacity fading mechanism and improvement of cycling stability in MoS2-based anode materials for lithium-ion batteries

    Science.gov (United States)

    Shu, Haibo; Li, Feng; Hu, Chenli; Liang, Pei; Cao, Dan; Chen, Xiaoshuang

    2016-01-01

    Two-dimensional (2D) layered MoS2 nanosheets possess great potential as anode materials for lithium ion batteries (LIBs), but they still suffer from poor cycling performance. Improving the cycling stability of electrode materials depends on a deep understanding of their dynamic structural evolution and reaction kinetics in the lithiation process. Herein, thermodynamic phase diagrams and the lithiation dynamics of MoS2-based nanostructures with the intercalation of lithium ions are studied by using first-principles calculations and ab initio molecular dynamics simulations. Our results demonstrate that the continuous intercalation of Li ions induces structural destruction of 2H phase MoS2 nanosheets in the discharge process that follows a layer-by-layer dissociation mechanism. Meanwhile, the intercalation of Li ions leads to a structural transition of MoS2 nanosheets from the 2H to the 1T phase due to the ultralow transition barriers (~0.1 eV). We find that the phase transition can slow down the dissociation of MoS2 nanosheets during lithiation. The result can be applied to explain extensive experimental observation of the fast capacity fading of MoS2-based anode materials between the first and the subsequent discharges. To suppress the dissociation of MoS2 nanosheets in the lithiation process, we propose a strategy by constructing a sandwich-like graphene/MoS2/graphene structure that indicates high chemical stability, superior conductivity, and high Li-ion mobility in the charge/discharge process, implying the possibility to induce an improvement in the anode cycling performance. This work opens a new route to rational design layered transition-metal disulfide (TMD) anode materials for LIBs with superior cycling stability and electrochemical performance.Two-dimensional (2D) layered MoS2 nanosheets possess great potential as anode materials for lithium ion batteries (LIBs), but they still suffer from poor cycling performance. Improving the cycling stability of

  13. Preparation of Gold Nanoparticles Deposited Silicon Thin Film Electrode by Self-Assembly Method for the Employment of an Anode Material for Lithium Secondary Batteries.

    Science.gov (United States)

    Halim, Martin; Kim, Jung Sub; Nguyen, Si Hieu; Jeon, Bup Ju; Lee, Joong Kee

    2015-10-01

    This work describes a self-assembly method of gold nanoparticles coating on the surface of silicon thin films for the anode material of lithium secondary batteries. The preparation of the silicon thin films was carried out by electron cyclotron resonance metal organic chemical vapor deposition (ECR-MOCVD) process. The obtained films were further coated with (3-aminopropyl)-trimethoxysilane (APTMS) which has a role to bind the oxygen functional groups on Si surface and the gold nanoparticles. The dispersed gold nanoparticles on the surface of silicon thin films could be prepared due to self-assembly phenomena which interact between attraction and repulsion in gold nanoparticles colloidal solution (GNCS). The use of reducing agent of sodium citrate and tannic acid in GNCS significantly affected the size of gold nanoparticle in our experimental range. Based on our experimental results, the higher reversible capacity was exhibited for the silicon that was immersed in the GNCS consisted of only sodium citrate. The GNCS consisted of both sodium citrate and tannic acid produced severe coagulated nanoparticles when deposited on the silicon surface and thus inhibited the lithium movement from electrolyte to silicon surface. Consequently, the reversible capacity of silicon anode material with coagulated gold nanoparticles coating showed the reduced performance. PMID:26726492

  14. A novel Co-Li2O@Si core-shell nanowire array composite as a high-performance lithium-ion battery anode material

    Science.gov (United States)

    Zhao, Wenjia; Du, Ning; Zhang, Hui; Yang, Deren

    2016-02-01

    We report a novel material of Co-Li2O@Si core-shell nanowire array synthesized via the lithiation of pre-synthesized CoO@Si core-shell nanowire arrays during the first cycle. When the potential window versus lithium was controlled between 0.01-1.2 V, the coated Si shell could be electrochemically active, while the Co-Li2O nanowire core could function as a stable mechanical support and an efficient electron conducting pathway during the charge-discharge process. The Co-Li2O@Si core-shell nanowire array anodes exhibit good cyclic stability and high power capability compared to planar Si film electrodes.We report a novel material of Co-Li2O@Si core-shell nanowire array synthesized via the lithiation of pre-synthesized CoO@Si core-shell nanowire arrays during the first cycle. When the potential window versus lithium was controlled between 0.01-1.2 V, the coated Si shell could be electrochemically active, while the Co-Li2O nanowire core could function as a stable mechanical support and an efficient electron conducting pathway during the charge-discharge process. The Co-Li2O@Si core-shell nanowire array anodes exhibit good cyclic stability and high power capability compared to planar Si film electrodes. Electronic supplementary information (ESI) available. See DOI: 10.1039/c5nr06120b

  15. Synthesis and Application of Si/Carbon Nanofiber Composites Based on Ni and Mo Catalysts for Anode Material of Lithium Secondary Batteries.

    Science.gov (United States)

    Jang, Eunyi; Park, Heal-Ku; Lee, Chang-Seop

    2016-05-01

    In this paper, carbon nanofibers (CNFs) and Si/carbon nanofiber composites were synthesized for use as the anode material of lithium secondary batteries. Catalysts were prepared based on Ni and Mo metals and CNFs were grown through chemical vapor deposition (CVD). In addition, the grown CNFs were mixed with silicon particles to synthesize Si/carbon nanofibers composites. The physiochemical characteristics of the synthesized CNFs and Si/carbon nanofiber composites were analyzed by SEM, EDS, XRD, Raman, BET and XPS. The electrochemical characteristics were investigated by using cyclic voltammetry and galvanostatic charge-discharge. Using CNFs and Si/carbon nanofiber composites as the anode material, three electrode cells were assembled and the electrochemical characteristics were measured using LiPF6 and LiClO4 as electrolytes. As a result of the galvanostatic charge-discharge of CNFs that were grown through catalysts with Ni and Mo concentration ratio of 6:4, the initial discharge capacity when using LiPF6 as the electrolyte was 570 mAh/g and the retention rate was 15.05%. In the case of using LiClO4 as the electrolyte, the initial discharge capacity was 263 mAh/g and the retention rate was 67.23%. PMID:27483824

  16. Hierarchical MoS2 tubular structures internally wired by carbon nanotubes as a highly stable anode material for lithium-ion batteries.

    Science.gov (United States)

    Chen, Yu Ming; Yu, Xin Yao; Li, Zhen; Paik, Ungyu; Lou, Xiong Wen David

    2016-07-01

    Molybdenum disulfide (MoS2), a typical two-dimensional material, is a promising anode material for lithium-ion batteries because it has three times the theoretical capacity of graphite. The main challenges associated with MoS2 anodes are the structural degradation and the low rate capability caused by the low intrinsic electric conductivity and large strain upon cycling. Here, we design hierarchical MoS2 tubular structures internally wired by carbon nanotubes (CNTs) to tackle these problems. These porous MoS2 tubular structures are constructed from building blocks of ultrathin nanosheets, which are believed to benefit the electrochemical reactions. Benefiting from the unique structural and compositional characteristics, these CNT-wired MoS2 tubular structures deliver a very high specific capacity of ~1320 mAh g(-1) at a current density of 0.1 A g(-1), exceptional rate capability, and an ultralong cycle life of up to 1000 cycles. This work may inspire new ideas for constructing high-performance electrodes for electrochemical energy storage. PMID:27453938

  17. Pulsed laser deposited Cr{sub 2}O{sub 3} nanostructured thin film on graphene as anode material for lithium-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Khamlich, S., E-mail: skhamlich@gmail.com [UNESCO-UNISA Africa Chair in Nanosciences-Nanotechnology, College of Graduate Studies, University of South Africa, Muckleneuk Ridge, PO Box 392, Pretoria (South Africa); Nanosciences African Network (NANOAFNET), iThemba LABS-National Research Foundation, 1 Old Faure Road, Somerset West 7129, PO Box 722, Somerset West, Western Cape Province (South Africa); Nuru, Z.Y. [UNESCO-UNISA Africa Chair in Nanosciences-Nanotechnology, College of Graduate Studies, University of South Africa, Muckleneuk Ridge, PO Box 392, Pretoria (South Africa); Nanosciences African Network (NANOAFNET), iThemba LABS-National Research Foundation, 1 Old Faure Road, Somerset West 7129, PO Box 722, Somerset West, Western Cape Province (South Africa); Bello, A.; Fabiane, M.; Dangbegnon, J.K.; Manyala, N. [Department of Physics, SARChI Chair in Carbon Technology and Materials, Institute of Applied Materials, University of Pretoria, Pretoria (South Africa); Maaza, M. [UNESCO-UNISA Africa Chair in Nanosciences-Nanotechnology, College of Graduate Studies, University of South Africa, Muckleneuk Ridge, PO Box 392, Pretoria (South Africa); Nanosciences African Network (NANOAFNET), iThemba LABS-National Research Foundation, 1 Old Faure Road, Somerset West 7129, PO Box 722, Somerset West, Western Cape Province (South Africa)

    2015-07-15

    Graphical abstract: A different approach for the fabrication of an anode material system that comprises pulsed laser-deposited (PLD) Cr{sub 2}O{sub 3} grown on few layer graphene (FLG) by chemical vapor deposition (CVD) was used. The electrochemical performance of Cr{sub 2}O{sub 3} nanostructured thin film was improved by FLG, which make it a promising candidate for future lithium-ion batteries application. - Highlights: • Pulsed laser deposition technique was used to deposit Cr{sub 2}O{sub 3} on few-layer graphene (FLG). • FLG improved the electrochemical performance of Cr{sub 2}O{sub 3} nanostructured thin film. • Good stable cycle of Cr{sub 2}O{sub 3}/FLG/Ni electrode make it one of the promise anode materials for future lithium-ion batteries. - Abstract: Pulsed laser deposition technique was used to deposit Cr{sub 2}O{sub 3} nanostructured thin film on a chemical vapor deposited few-layer graphene (FLG) on nickel (Ni) substrate for application as anode material for lithium-ion batteries. The experimental results show that graphene can effectively enhance the electrochemical property of Cr{sub 2}O{sub 3}. For Cr{sub 2}O{sub 3} thin film deposited on Ni (Cr{sub 2}O{sub 3}/Ni), a discharge capacity of 747.8 mA h g{sup −1} can be delivered during the first lithiation process. After growing Cr{sub 2}O{sub 3} thin film on FLG/Ni, the initial discharge capacity of Cr{sub 2}O{sub 3}/FLG/Ni was improved to 1234.5 mA h g{sup −1}. The reversible lithium storage capacity of the as-grown material is 692.2 mA h g{sup −1} after 100 cycles, which is much higher than that of Cr{sub 2}O{sub 3}/Ni (111.3 mA h g{sup −1}). This study reveals the differences between the two material systems and emphasizes the role of the graphene layers in improving the electrochemical stability of the Cr{sub 2}O{sub 3} nanostructured thin film.

  18. Biomass carbon micro/nano-structures derived from ramie fibers and corncobs as anode materials for lithium-ion and sodium-ion batteries

    Science.gov (United States)

    Jiang, Qiang; Zhang, Zhenghao; Yin, Shengyu; Guo, Zaiping; Wang, Shiquan; Feng, Chuanqi

    2016-08-01

    Three-dimensional (3D) rod-like carbon micro-structures derived from natural ramie fibers and two-dimensional (2D) carbon nanosheets derived from corncobs have been fabricated by heat treatment at 700 °C under argon atomsphere. The structure and morphology of the as-obtained ramie fiber carbon (RFC) and corncob carbon (CC) were characterized by X-ray diffraction (XRD), Raman spectroscopy, scanning electron microscopy (SEM) and transmission electron microscopy (TEM) technique. The electrochemical performances of the biomass carbon-based anode in lithium-ion batteries (LIBs) and sodium-ion batteries (SIBs) were investigated. When tested as anode material for lithium ion batteries, both the RFC microrods and CC nanosheets exhibited high capacity, excellent rate capability, and stable cyclability. The specific capacity were still as high as 489 and 606 mAhg-1 after 180 cycles when cycled at room temperature in a 3.0-0.01 V potential (vs. Li/Li+) window at current density of 100 mAg-1, respectively, which are much higher than that of graphite (375 mAhg-1) under the same current density. Although the anodes in sodium ion batteries showed poorer specific capability than that in lithium-ion batteries, they still achieve a reversible sodium intercalation capacity of 122 and 139 mAhg-1 with similar cycling stability. The feature of stable cycling performance makes the biomass carbon derived from natural ramie fibers and corncobs to be promising candidates as electrodes in rechargeable sodium-ion batteries and lithium-ion batteries.

  19. Self-discharge of LiSi and LiB anode materials%LiSi和LiB负极材料的自放电性能

    Institute of Scientific and Technical Information of China (English)

    袁光明; 高文秀; 李成; 赵小玲; 郑奕; 刘波

    2015-01-01

    The capacity decay occurs due to the self-discharge after activation in the molten salt electrolyte lithium batteries. Using LiF-LiCl-LiBr molten salts as electrolyte and FeS2 as cathode material, the lithium-silicon alloy and lithium-boron alloy as anode material to prepare single cells, which was then discharged at constant currents and 500℃. The working time of the single cells can be adjusted simply by varying the discharge current, the change of the available capacity is obtained. The working time and the measured capacity were analyzed by unary linear regression. The results show that the rate of the capacity loss is 40.6 C/min when lithium-silicon alloy is used as anode material, which is only 15.5 C/min when lithium-boron alloy is used as anode material.%熔盐电解质锂电池在激活后由于自放电导致容量发生衰减,采用LiF-LiCl-LiBr低温共熔盐电解质,以二硫化铁为正极材料,分别以锂硅合金和锂硼合金作为负极材料制备单体电池,在500℃的温度下进行恒流放电试验。通过改变单体电池的工作电流可控制电池放电时间,并得到单体电池在经历不同工作时间后获得的可利用电容量。并将单体电池的工作时间和可利用电容量经一次线性回归分析。结果发现,使用锂硅合金作为负极材料时,电池的容量衰减率为40.6 C/min;而使用锂硼合金作为负极材料时,电池的容量衰减率仅为15.5 C/min。

  20. 锂离子电池用硅基材料的研究进展%Research progress of silicon material as anode for lithium-ion batteries

    Institute of Scientific and Technical Information of China (English)

    李涛; 杨娟玉; 卢世刚

    2012-01-01

    锂离子电池硅基负极材料以其较高的理论比容量(4 200 nAh/g),成为最具吸引力的新一代负极材料.但硅基负极材料较差的循环性能和较大的首次不可逆容量损失导致其商业化应用受科限制.研究者采取了各种方法来克服硅基材料在嵌脱锂过程中较大的体积变化对电极结构的破坏,从而获得了较好的容量保持率和循环性能,其中包括纳米化、复合化和薄膜化等材料体系的改性,选择不同的粘接剂、导电剂等电极制备方法的改进,以及选择不同电解液和控制电压窗口等电池实际应用方面的措施.主要介绍了近年来硅基负极改性方法方面的研究进展,探讨了硅基材料应用中的问题及可能的解决方法.%Silicon materials are attractive candidates for the next generation of fithium-ion batteries due to their high theoretical specific capacities (4 200 mAh/g).However,the commercial use of silicon anodes has been hindered to date by their low cycle life and high initial capacity loss.To overcome the damage of the electrode from the targe volume change and thus obtain better capacity retention and cycle life for Si anodes,various approaches have been used: using nano-partictes,forming multiphase composites,fabricating thin film electrodes and alloys,using selected binders and electrolyte,operating vottage control,et al.Here,the methodologies adopted for reducing the capacity fade observed in silicon-based anodes were reviewed,the challenges that remained in using silicon and silicon-based anodes were discussed,and the possible approaches for overcoming them were proposed.

  1. Graphene-Wrapped Anatase TiO2 Nanofibers as High-Rate and Long-Cycle-Life Anode Material for Sodium Ion Batteries

    Science.gov (United States)

    Yeo, Yeolmae; Jung, Ji-Won; Park, Kyusung; Kim, Il-Doo

    2015-09-01

    Anatase TiO2 has been suggested as a potential sodium anode material, but the low electrical conductivity of TiO2 often limits the rate capability, resulting in poor electrochemical properties. To address this limitation, we propose graphene-wrapped anatase TiO2 nanofibers (rGO@TiO2 NFs) through an effective wrapping of reduced graphene oxide (rGO) sheets on electrospun TiO2 NFs. To provide strong electrostatic interaction between the graphene oxide (GO) sheets and the TiO2 NFs, poly(allylamine hydrochloride) (PAH) was used to induce a positively charged TiO2 surface by the immobilization of the -NH3+ group and to promote bonding with the negatively charged carboxylic acid (-COO-) and hydroxyl (-O-) groups on the GO. A sodium anode electrode using rGO@TiO2 NFs exhibited a significantly improved initial capacity of 217 mAh g-1, high capacity retention (85% after 200 cycles at 0.2C), and a high average Coulombic efficiency (99.7% from the second cycle to the 200th cycle), even at a 5C rate, compared to those of pristine TiO2 NFs. The improved electrochemical performances stem from highly conductive properties of the reduced GO which is effectively anchored to the TiO2 NFs.

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

    Science.gov (United States)

    Siwińska-Stefańska, Katarzyna; Kurc, Beata

    2015-12-01

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

  3. 锂离子电池用石墨烯基负极材料的研究进展%Research progress in graphene-based anode material for Li-ion battery

    Institute of Scientific and Technical Information of China (English)

    高云雷; 赵东林; 白利忠; 景磊

    2012-01-01

    综述了石墨烯和石墨烯基复合材料作为锂离子电池负极材料的研究进展,重点论述了金属氧化物/石墨烯复合材料,对石墨烯基复合材料的发展趋势进行了展望.%Research progress in Li-ion battery anode material ineluding graphene and graphene-based composite was reviewed. Metal oxide/graphene composite was mainly discussed,the development trend of graphene-based anode material was prospected.

  4. Facile scalable synthesis of Co{sub 3}O{sub 4}/carbon nanotube hybrids as superior anode materials for lithium-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Fang, Zhiguo; Xu, Weiwei [Key Lab of Synthetic and Natural Functional Molecule Chemistry of Ministry of Education, and the College of Chemistry and Materials Science, Northwest University, Xi’an 710069 (China); Huang, Tao [Department of Chemistry, Fudan University, Shanghai 210024 (China); Li, Maolin; Wang, Wanren; Liu, Yanping; Mao, Chaochao; Meng, Fanli; Wang, Mengjiao [Key Lab of Synthetic and Natural Functional Molecule Chemistry of Ministry of Education, and the College of Chemistry and Materials Science, Northwest University, Xi’an 710069 (China); Cheng, Minghai [Suzhou Institute of Nano-Tech and Nano-Bionics, Chinese Academy of Sciences (China); Yu, Aishui [Department of Chemistry, Fudan University, Shanghai 210024 (China); Guo, Xiaohui, E-mail: guoxh2009@nwu.edu.cn [Key Lab of Synthetic and Natural Functional Molecule Chemistry of Ministry of Education, and the College of Chemistry and Materials Science, Northwest University, Xi’an 710069 (China)

    2013-10-15

    Graphical abstract: Co{sub 3}O{sub 4}/MWCNT hybrids were synthesized via strong ultra-sonication assisted shaking processes. The resultant samples as anode electrode display enhanced cycling performance and rate capability compared with pure Co{sub 3}O{sub 4} particle. - Highlights: • Co{sub 3}O{sub 4}/MWCNT hybrids were synthesized via ultra-sonication assisted shaking process. • The resulting Co{sub 3}O{sub 4} nanoparticles are highly dispersed onto MWCNT network backbone. • Co{sub 3}O{sub 4}/MWCNT hybrid displays highly enhanced lithium storage properties. • The present synthetic approach is facile, controllable, and scalable. - Abstract: In this report, Co{sub 3}O{sub 4}/multiple-wall carbon nanotube (MWCNT) hybrid materials were synthesized via strong ultrasonication-assisted shaking and magnetic stirring processes. The prepared samples were well characterized by utilizing powder X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and Raman spectroscopy techniques. Results indicated that the resulting Co{sub 3}O{sub 4} nanoparticles were highly dispersed in the MWCNT network backbone and further form Co{sub 3}O{sub 4}/MWCNT hybrid materials. The obtained Co{sub 3}O{sub 4}/MWCNT hybrids can be employed as anode electrode in Lithium-ion batteries and deliver as high as discharge capacity of 1250 mA h g{sup −1} at a current density of 0.2 C, additionally, 81% of the discharge capacity for sample 2 with 20 wt.% MWCNT loading could be retained after 70 cycles, which could be associated with the specific hybrid structure of the electrode as well as the addition of MWCNT. Most importantly, the present synthetic approach is facile, controllable, and scalable, which allowing it more easily adapted to prepare other hybrid materials with specific architectures.

  5. Novel synthetic approach for 1, 4-dihydroxyanthraquinone and the development of its Lithiated salts as anode material for aqueous rechargeable Lithium-ion batteries

    KAUST Repository

    Gurukar, Suresh Shivappa

    2015-08-17

    The influence of organic electrode materials in the field of lithium ion battery is becoming a keen interest for the present generation scientists. Here we are reporting a novel method of synthesis of electrode material by the combination of sono-chemical and thermal methods. The advantages of organic active material towards lithium ion battery are of core interest of this study. The structural confirmations are by FT-IR, 1H NMR, MALDI-TOF Mass Spectroscopy and powder XRD data. The electrochemical properties of Lithiated-1,4-dihydroxyanthraquinone were studied using electrochemical-techniques such as Cyclic Voltammetry, Galvanostatic Cyclic Potential Limitation and Potentiostatic Electrochemical Impedance Spectroscopy. The satisfactory results towards stability of active species in the aqueous media, reasonable discharge capacity with 0.9 V average voltages and agreeable cycling performance during charge-discharge process with reproducibility are achieved. For the construction of the full cell, the anode material was coupled with the LiNi1/3Co1/3Mn1/3O2 as a cathode material.

  6. Unique 1D Co3O4 crystallized nanofibers with (220) oriented facets as high-performance lithium ion battery anode material

    Science.gov (United States)

    Tan, Yanli; Gao, Qiuming; Li, Zeyu; Tian, Weiqian; Qian, Weiwei; Yang, Chunxiao; Zhang, Hang

    2016-01-01

    A novel one-step hydrothermal and calcination strategy was developed to synthesize the unique 1D oriented Co3O4 crystal nanofibers with (220) facets on the carbon matrix derived from the natural, abundant and low cost wool fibers acting as both carbon precursor and template reagent. The resultant W2@Co3O4 nanocomposite exhibited very high specific capacity and favorable high-rate capability when used as anode material of lithium ion battery. The high reversible Li+ ion storage capacity of 986 mAh g−1 was obtained at 100 mA g−1 after 150 cycles, higher than the theoretical capacity of Co3O4 (890 mAh g−1). Even at the higher current density of 1 A g−1, the electrode could still deliver a remarkable discharge capacity of 720 mAh g−1 over 150 cycles. PMID:27217201

  7. Self-assembled graphene-wrapped SnO{sub 2} nanotubes nanohybrid as a high-performance anode material for lithium-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Wu, Ping, E-mail: zjuwuping@njnu.edu.cn; Xu, Xiali; Zhu, Qingyun; Zhu, Xiaoshu; Tang, Yawen; Zhou, Yiming, E-mail: zhouyiming@njnu.edu.cn; Lu, Tianhong

    2015-03-25

    Highlights: • SnO{sub 2}-NTs/G nanohybrid prepared via a facile Sn-nanorod-templated self-assembly route. • 3D interconnected network of SnO{sub 2} nanotubes wrapped and bridged by graphene matrix. • Superior lithium storage performance by virtue of its unique structural features. - Abstract: Herein, a novel type of graphene-wrapped SnO{sub 2} nanotubes (SnO{sub 2}-NTs/G) nanohybrid has been designed and constructed through a facile Sn-nanorod-templated self-assembly approach. The as-prepared SnO{sub 2}-NTs/G nanohybrid has been utilized as an anode material in lithium-ion batteries, and demonstrates remarkable cycling stability, high reversible capacities, and rate capability by virtue of its unique structural features.

  8. Self-assembled three-dimensional hierarchical NiO nano/microspheres as high-performance anode material for lithium ion batteries

    International Nuclear Information System (INIS)

    Highlights: • 3D hierarchical NiO porous nano/microspheres were prepared via a hydrothermal route. • Loose NiO microsphere is composed of a large number of cross-linked nanoparticles. • A possible self-assembly mechanism is illustrated in detail. • High specific capacity, good cycleability and superior rate-capability are achieved. - Abstract: Self-assembled three-dimensional hierarchical NiO nano/microspheres were fabricated via a hydrothermal route. The obtained NiO presents a micro-sized porous spherical morphology which is composed of a large number of primary NiO nanoparticles linked together with an ordered fashion. As anode material for lithium ion batteries, NiO nano/microspheres exhibit stable reversible capacity of over 700 mAh g−1 and good rate capability. The superior electrochemical performance could be attributed to the merits of the unique three-dimensional hierarchical porous nano/microstructure

  9. A ternary phased SnO2-Fe2O3/SWCNTs nanocomposite as a high performance anode material for lithium ion batteries

    Institute of Scientific and Technical Information of China (English)

    Wangliang Wu; Yi Zhao; Jiaxin Li; Chuxin Wu; Lunhui Guan

    2014-01-01

    A new SnO2-Fe2O3/SWCNTs (single-walled carbon nanotubes) ternary nanocomposite was first synthesized by a facile hydrothermal ap-proach. SnO2 and Fe2O3 nanoparticles (NPs) were homogeneously located on the surface of SWCNTs, as confirmed by X-ray diffraction (XRD), transmission electron microscope (TEM) and energy dispersive X-ray spectroscopy (EDX). Due to the synergistic effect of different components, the as synthesized SnO2-Fe2O3/SWCNTs composite as an anode material for lithium-ion batteries exhibited excellent electro-chemical performance with a high capacity of 692 mAh·g-1 which could be maintained after 50 cycles at 200 mA·g-1. Even at a high rate of 2000 mA·g-1, the capacity was still remained at 656 mAh·g-1.

  10. Fabrication of boron-doped carbon fibers by the decomposition of B4C and its excellent rate performance as an anode material for lithium-ion batteries

    Science.gov (United States)

    Wang, Huiqi; Ma, Canliang; Yang, Xueteng; Han, Tao; Tao, Zechao; Song, Yan; Liu, Zhanjun; Guo, Quangui; Liu, Lang

    2015-03-01

    A facile route, for the first time, was developed to fabricate boron-doped carbon fibers (BDCFs). Boron was doped into mesosphere pitch-based carbon fibers (CFs) by exposing the CFs in a vapor of boron by the decomposition of boron carbide. The microstructure of BDCFs was characterized by SEM, TEM, XRD and Raman spectroscopy. When used as anode materials for the lithium-ion batteries, BDCFs electrode exhibits an improved performance. Concretely, the specific capacity of BDCFs still had a value of over 400 mAh g-1 after 100 cycles. Moreover, BDCFs exhibits better rate capability and less hysteresis in comparison to the pristine CFs. Such enhanced lithium storage capability can be attributed to the improvement of graphitization properties and the high amount of defects induced by boron.

  11. A Novel Ion-exchange Method for the Synthesis of Nano-SnO/micro-C Hybrid Structure as High Capacity Anode Material in Lithium Ion Batteries

    Institute of Scientific and Technical Information of China (English)

    Zhi Tan; Zhenhua Sun; Qi Guo; Haihua Wang; Dangsheng Su

    2013-01-01

    A novel and simple ion-exchange method was developed for the synthesis of nano-SnO/micro-C hybrid structure.The structure of the as prepared nano-SnO/micro-C was directly revealed by scanning electron microscopy (SEM)and transmission electron microscopy (TEM).SnO particles with the size about 25 nm were well confined in amorphous carbon microparticles.Carbon matrix in micrometer scale not only acts as a protective buffer for the SnO nanoparticles during the battery cycling processes,but also avoids the shortcomings of nanostructures,such as low tap density and potential safety threats.Electrochemical behaviors of the nano-SnO/micro-C were tested as anode material in lithium ion batteries.The initial reversible capacity is 508 mA h g-1,and the reversible capacity after 60 cycles is 511 mA h g-1,indicating good capacity retention ability.

  12. Unique 1D Co3O4 crystallized nanofibers with (220) oriented facets as high-performance lithium ion battery anode material

    Science.gov (United States)

    Tan, Yanli; Gao, Qiuming; Li, Zeyu; Tian, Weiqian; Qian, Weiwei; Yang, Chunxiao; Zhang, Hang

    2016-05-01

    A novel one-step hydrothermal and calcination strategy was developed to synthesize the unique 1D oriented Co3O4 crystal nanofibers with (220) facets on the carbon matrix derived from the natural, abundant and low cost wool fibers acting as both carbon precursor and template reagent. The resultant W2@Co3O4 nanocomposite exhibited very high specific capacity and favorable high-rate capability when used as anode material of lithium ion battery. The high reversible Li+ ion storage capacity of 986 mAh g‑1 was obtained at 100 mA g‑1 after 150 cycles, higher than the theoretical capacity of Co3O4 (890 mAh g‑1). Even at the higher current density of 1 A g‑1, the electrode could still deliver a remarkable discharge capacity of 720 mAh g‑1 over 150 cycles.

  13. A three-dimensional porous MoP@C hybrid as a high-capacity, long-cycle life anode material for lithium-ion batteries

    Science.gov (United States)

    Wang, Xia; Sun, Pingping; Qin, Jinwen; Wang, Jianqiang; Xiao, Ying; Cao, Minhua

    2016-05-01

    Metal phosphides are great promising anode materials for lithium-ion batteries with a high gravimetric capacity. However, significant challenges such as low capacity, fast capacity fading and poor cycle stability must be addressed for their practical applications. Herein, we demonstrate a versatile strategy for the synthesis of a novel three-dimensional porous molybdenum phosphide@carbon hybrid (3D porous MoP@C hybrid) by a template sol-gel method followed by an annealing treatment. The resultant hybrid exhibits a 3D interconnected ordered porous structure with a relatively high surface area. Benefiting from its advantages of microstructure and composition, the 3D porous MoP@C hybrid displays excellent lithium storage performance as an anode material for lithium-ion batteries in terms of specific capacity, cycling stability and long-cycle life. It presents stable cycling performance with a high reversible capacity up to 1028 mA h g-1 at a current density of 100 mA g-1 after 100 cycles. By ex situ XRD, HRTEM, SAED and XPS analyses, the 3D porous MoP@C hybrid was found to follow the Li-intercalation reaction mechanism (MoP + xLi+ + e- LixMoP), which was further confirmed by ab initio calculations based on density functional theory.Metal phosphides are great promising anode materials for lithium-ion batteries with a high gravimetric capacity. However, significant challenges such as low capacity, fast capacity fading and poor cycle stability must be addressed for their practical applications. Herein, we demonstrate a versatile strategy for the synthesis of a novel three-dimensional porous molybdenum phosphide@carbon hybrid (3D porous MoP@C hybrid) by a template sol-gel method followed by an annealing treatment. The resultant hybrid exhibits a 3D interconnected ordered porous structure with a relatively high surface area. Benefiting from its advantages of microstructure and composition, the 3D porous MoP@C hybrid displays excellent lithium storage performance as an

  14. Facile Synthesis of Mn-Doped ZnO Porous Nanosheets as Anode Materials for Lithium Ion Batteries with a Better Cycle Durability.

    Science.gov (United States)

    Wang, Linlin; Tang, Kaibin; Zhang, Min; Xu, Jingli

    2015-12-01

    Porous Zn1 - x Mn x O (x = 0.1, 0.2, 0.44) nanosheets were prepared by a low-cost, large-scale production and simple approach, and the applications of these nanosheets as an anode material for Li-ion batteries (LIBs) were explored. Electrochemical measurements showed that the porous Zn0.8Mn0.2O nanosheets still delivered a stable reversible capacity of 210 mA h g(-1) at a current rate of 120 mA g(-1) up to 300 cycles. These results suggest that the facile synthetic method of producing porous Zn0.8Mn0.2O nanostructure can realize a better cycle durability with stable reversible capacity. PMID:26138451

  15. Layered nickel sulfide-reduced graphene oxide composites synthesized via microwave-assisted method as high performance anode materials of sodium-ion batteries

    Science.gov (United States)

    Qin, Wei; Chen, Taiqiang; Lu, Ting; Chua, Daniel H. C.; Pan, Likun

    2016-01-01

    Layered nickel sulfide (NS)-reduced graphene oxide (RGO) composites are prepared via a simple microwave-assisted method and subsequent annealing in N2/H2 atmosphere. A detailed array of characterization tools are used to study their morphology, structure and electrochemical performance. It was found that these composites exhibit significantly improved sodium-ion storage ability as compared with pure NS under galvanostatic cycling at a specific current of 100 mA g-1 in a potential limitation of 0.005-3.0 V. Furthermore, the composite with the RGO content of 35 wt.% achieves a high maximum reversible specific capacity of about 391.6 mAh g-1 at a specific current of 100 mA g-1 after 50 cycles. These results prove that NS-RGO composites are highly promising when applied directly as anode materials in sodium-ion batteries.

  16. Synthesis of SnO2 pillared carbon using long chain alkylamine grafted graphene oxide: an efficient anode material for lithium ion batteries

    Science.gov (United States)

    Reddy, M. Jeevan Kumar; Ryu, Sung Hun; Shanmugharaj, A. M.

    2015-12-01

    With the objective of developing new advanced composite materials that can be used as anodes for lithium ion batteries (LIBs), herein we describe the synthesis of SnO2 pillared carbon using various alkylamine (hexylamine; dodecylamine and octadecylamine) grafted graphene oxides and butyl trichlorotin precursors followed by its calcination at 500 °C for 2 h. While the grafted alkylamine induces crystalline growth of SnO2 pillars, thermal annealing of alkylamine grafted graphene oxide results in the formation of amorphous carbon coated graphene. Field emission scanning electron microscopy (FE-SEM) results reveal the successful formation of SnO2 pillared carbon on the graphene surface. X-ray diffraction (XRD), transmission electron microscopy (TEM) and Raman spectroscopy characterization corroborates the formation of rutile SnO2 crystals on the graphene surface. A significant rise in the BET surface area is observed for SnO2 pillared carbon, when compared to pristine GO. Electrochemical characterization studies of SnO2 pillared carbon based anode materials showed an enhanced lithium storage capacity and fine cyclic performance in comparison with pristine GO. The initial specific capacities of SnO2 pillared carbon are observed to be 1379 mA h g-1, 1255 mA h g-1 and 1360 mA h g-1 that decrease to 750 mA h g-1, 643 mA h g-1 and 560 mA h g-1 depending upon the chain length of grafted alkylamine on the graphene surface respectively. Electrochemical impedance spectral analysis reveals that the exchange current density of SnO2 pillared carbon based electrodes is higher, corroborating its enhanced electrochemical activity in comparison with GO based electrodes.With the objective of developing new advanced composite materials that can be used as anodes for lithium ion batteries (LIBs), herein we describe the synthesis of SnO2 pillared carbon using various alkylamine (hexylamine; dodecylamine and octadecylamine) grafted graphene oxides and butyl trichlorotin precursors

  17. Synthesis and electrochemical performance of cable-like copper vanadates/polypyrrole nanobelts as anode materials for lithium-ion batteries

    Science.gov (United States)

    Zhang, Shaoyan; Hou, Menghua; Hou, Linlin; Lu, Min

    2016-08-01

    Cable-like CuV2O6/polypyrrole (CVO/PPy) nanobelts have been synthesized via in-situ oxidative polymerization of pyrrole monomers on the surface of hydrothermally synthesized α-CuV2O6 (CVO) nanobelts. The microscope analysis revealed that the diameter of cable-like CVO/PPy nanobelts focused on 80-110 nm and the shell thickness was about 10-30 nm. The electrochemical properties of the cable-like CVO/PPy nanobelts as anode materials were systematically investigated and compared with bare α-CuV2O6 nanobelts. It was found that the electrochemical performance of the CVO/PPy nanobelts was significantly enhanced. The results suggest that the conductive PPy nanolayer coating help to preserve high capacity, maintain high electrochemical stability, and reduce charge transfer resistance during cycling performance.

  18. Soft template strategy to synthesize iron oxide-titania yolk-shell nanoparticles as high-performance anode materials for lithium-ion battery applications.

    Science.gov (United States)

    Lim, Joohyun; Um, Ji Hyun; Ahn, Jihoon; Yu, Seung-Ho; Sung, Yung-Eun; Lee, Jin-Kyu

    2015-05-18

    Yolk-shell-structured nanoparticles with iron oxide core, void, and a titania shell configuration are prepared by a simple soft template method and used as the anode material for lithium ion batteries. The iron oxide-titania yolk-shell nanoparticles (IO@void@TNPs) exhibit a higher and more stable capacity than simply mixed nanoparticles of iron oxide and hollow titania because of the unique structure obtained by the perfect separation between iron oxide nanoparticles, in combination with the adequate internal void space provided by stable titania shells. Moreover, the structural effect of IO@void@TNPs clearly demonstrates that the capacity retention value after 50 cycles is approximately 4 times that for IONPs under harsh operating conditions, that is, when the temperature is increased to 80 °C.

  19. Designed hybrid nanostructure with catalytic effect: beyond the theoretical capacity of SnO2 anode material for lithium ion batteries

    Science.gov (United States)

    Wang, Ye; Huang, Zhi Xiang; Shi, Yumeng; Wong, Jen It; Ding, Meng; Yang, Hui Ying

    2015-01-01

    Transition metal cobalt (Co) nanoparticle was designed as catalyst to promote the conversion reaction of Sn to SnO2 during the delithiation process which is deemed as an irreversible reaction. The designed nanocomposite, named as SnO2/Co3O4/reduced-graphene-oxide (rGO), was synthesized by a simple two-step method composed of hydrothermal (1st step) and solvothermal (2nd step) synthesis processes. Compared to the pristine SnO2/rGO and SnO2/Co3O4 electrodes, SnO2/Co3O4/rGO nanocomposites exhibit significantly enhanced electrochemical performance as the anode material of lithium-ion batteries (LIBs). The SnO2/Co3O4/rGO nanocomposites can deliver high specific capacities of 1038 and 712 mAh g−1 at the current densities of 100 and 1000 mA g−1, respectively. In addition, the SnO2/Co3O4/rGO nanocomposites also exhibit 641 mAh g−1 at a high current density of 1000 mA g−1 after 900 cycles, indicating an ultra-long cycling stability under high current density. Through ex-situ TEM analysis, the excellent electrochemical performance was attributed to the catalytic effect of Co nanoparticles to promote the conversion of Sn to SnO2 and the decomposition of Li2O during the delithiation process. Based on the results, herein we propose a new method in employing the catalyst to increase the capacity of alloying-dealloying type anode material to beyond its theoretical value and enhance the electrochemical performance. PMID:25776280

  20. Anatase-TiO{sub 2}/CNTs nanocomposite as a superior high-rate anode material for lithium-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Jinlong [College of Chemistry and Chemical Engineering, Central South University, Changsha 410083 (China); State Key Laboratory of Powder Metallurgy, Central South University, Changsha 410083 (China); Feng, Haibo; Jiang, Jianbo [College of Chemistry and Chemical Engineering, Central South University, Changsha 410083 (China); Qian, Dong, E-mail: qiandong6@vip.sina.com [College of Chemistry and Chemical Engineering, Central South University, Changsha 410083 (China); State Key Laboratory of Powder Metallurgy, Central South University, Changsha 410083 (China); Li, Junhua; Peng, Sanjun [College of Chemistry and Chemical Engineering, Central South University, Changsha 410083 (China); Liu, Youcai, E-mail: liuyoucai@126.com [College of Chemistry and Chemical Engineering, Central South University, Changsha 410083 (China)

    2014-08-01

    Highlights: • Anatase-TiO{sub 2}/CNTs nanocomposite was prepared by a facile and scalable hydrolysis route. • The composite exhibits super-high rate capability and excellent cycling stability for LIBs. • The nanocomposite shows great potential as a superior anode material for LIBs. - Abstract: Anatase-TiO{sub 2}/carbon nanotubes (CNTs) with robust nanostructure is fabricated via a facile two-step synthesis by ammonia water assisted hydrolysis and subsequent calcination. The as-synthesized nanocomposite was characterized employing X-ray powder diffraction, Fourier transform infrared spectrophotometry, Raman spectrophotometry, thermal gravimetric analysis, transmission electron microscopy, high-resolution transmission electron microscopy and selected area electronic diffraction, and its electrochemical properties as an anode material for lithium-ion batteries (LIBs) were investigated by cyclic voltammetry, galvanostatic discharge/charge test and electrochemical impendence spectroscopy. The results show that the pure anatase TiO{sub 2} nanoparticles with diameters of about 10 nm are uniformly distributed on/among the CNTs conducting network. The as-synthesized nanocomposite exhibits remarkably improved performances in LIBs, especially super-high rate capability and excellent cycling stability. Specifically, a reversible capacity as high as 92 mA h g{sup −1} is achieved even at a current density of 10 A g{sup −1} (60 C). After 100 cycles at 0.1 A g{sup −1}, it shows good capacity retention of 185 mA h g{sup −1} with an outstanding coulombic efficiency up to 99%. Such superior Li{sup +} storage properties demonstrate the reinforced synergistic effects between the nano-sized TiO{sub 2} and the interweaved CNTs network, endowing the nanocomposite with great application potential in high-power LIBs.

  1. Designed hybrid nanostructure with catalytic effect: beyond the theoretical capacity of SnO2 anode material for lithium ion batteries

    Science.gov (United States)

    Wang, Ye; Huang, Zhi Xiang; Shi, Yumeng; Wong, Jen It; Ding, Meng; Yang, Hui Ying

    2015-03-01

    Transition metal cobalt (Co) nanoparticle was designed as catalyst to promote the conversion reaction of Sn to SnO2 during the delithiation process which is deemed as an irreversible reaction. The designed nanocomposite, named as SnO2/Co3O4/reduced-graphene-oxide (rGO), was synthesized by a simple two-step method composed of hydrothermal (1st step) and solvothermal (2nd step) synthesis processes. Compared to the pristine SnO2/rGO and SnO2/Co3O4 electrodes, SnO2/Co3O4/rGO nanocomposites exhibit significantly enhanced electrochemical performance as the anode material of lithium-ion batteries (LIBs). The SnO2/Co3O4/rGO nanocomposites can deliver high specific capacities of 1038 and 712 mAh g-1 at the current densities of 100 and 1000 mA g-1, respectively. In addition, the SnO2/Co3O4/rGO nanocomposites also exhibit 641 mAh g-1 at a high current density of 1000 mA g-1 after 900 cycles, indicating an ultra-long cycling stability under high current density. Through ex-situ TEM analysis, the excellent electrochemical performance was attributed to the catalytic effect of Co nanoparticles to promote the conversion of Sn to SnO2 and the decomposition of Li2O during the delithiation process. Based on the results, herein we propose a new method in employing the catalyst to increase the capacity of alloying-dealloying type anode material to beyond its theoretical value and enhance the electrochemical performance.

  2. Preparation of Carbon-Encapsulated ZnO Tetrahedron as an Anode Material for Ultralong Cycle Life Performance Lithium-ion Batteries

    International Nuclear Information System (INIS)

    Highlights: • A novel architecture of 3D carbon framework to encapsulate ZnO nanocrystals was prepared. • The ZnO@C exhibits ultralong cycle life and high specific capacity when was used as anode. • The in situ carbonization leads to a strong connection between the carbon and ZnO. - ABSTRACT: In this paper we report a novel architecture of three-dimension (3D) carbon framework to encapsulate tetrahedron ZnO nanocrystals that serves as an anode material for lithium-ion batteries (LIBs). The ZnO@C composites are prepared via a simple internal-reflux method combined with subsequent calcination in argon. The amorphous carbon is formed on the surface of the ZnO crystals by in situ carbonization of the surfactant, which leads to a strong connection between the carbon framework and the active materials and guarantees faster charge transfer on the electrode. The ZnO crystal calcined at 500°C (ZnO@C-5) possesses regular tetrahedron shape with a side length of 150-200 nm and all of them are uniformly anchored among the network of amorphous carbon. The developed ZnO@C structures not only improve the electronic conductivity of the electrode, but they also offer a larger volume expansion of ZnO during cycling. As a result, the ZnO@C-5 demonstrates a higher reversible capacity, ultralong cycle life and better rate capability than that of the ZnO@C-7 and pure ZnO crystals. After 300 cycles, the ZnO@C-5 demonstrates a high capacity of 518 mAhg−1 at a current density of 110.7 mAg−1. Moreover, this simple approach prepared the 3D composites architecture could shed light on the design and synthesis of other transition metal oxides for energy storage

  3. One-step solution combustion synthesis of Fe{sub 2}O{sub 3}/C nano-composites as anode materials for lithium ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Li, Peiyang; Deng, Jiachun; Li, Ying [Nano-Energy Inorganic Materials Laboratory, College of Materials Science and Engineering, Taiyuan University of Technology, Taiyuan 030024 (China); Liang, Wei, E-mail: liangwei@tyut.edu.cn [Nano-Energy Inorganic Materials Laboratory, College of Materials Science and Engineering, Taiyuan University of Technology, Taiyuan 030024 (China); Wang, Kun [Nano-Energy Inorganic Materials Laboratory, College of Materials Science and Engineering, Taiyuan University of Technology, Taiyuan 030024 (China); Kang, Litao, E-mail: kangltxy@gmail.com [Nano-Energy Inorganic Materials Laboratory, College of Materials Science and Engineering, Taiyuan University of Technology, Taiyuan 030024 (China); Zeng, Shaozhong; Yin, Shanhui; Zhao, Zhigang [Chery Automobile Co. Ltd., Wuhu 241006 (China); Liu, Xuguang; Yang, Yongzhen [College of Chemistry and Chemical Engineering, Taiyuan University of Technology, Taiyuan 030024 (China); Gao, Feng [State Key Laboratory of Coal Conversion, Institute of Coal Chemistry, Chinese Academy of Sciences, Taiyuan 030001 (China)

    2014-03-25

    Highlights: • Fe{sub 2}O{sub 3}/C composite anode materials were prepared by a solution combustion process. • The carbon content could be adjusted by regulating the ratio of oxidizer/fuel. • The Fe{sub 2}O{sub 3}/C composite showed capacity 470 mA h g{sup −1} at the 80th cycle at 125 mA g{sup −1}. -- Abstract: This article describes a one-step solution combustion route (within 30 min at 350 °C in air) to prepare Fe{sub 2}O{sub 3} anode materials for lithium ion batteries (LIBs) from Fe(NO{sub 3}){sub 3}⋅9H{sub 2}O solution with citric acid. XRD, SEM-EDX and TEM showed that the product consisted a mixture of nano-sized α-Fe{sub 2}O{sub 3} and γ-Fe{sub 2}O{sub 3} crystals that agglomerated into porous particles. Significantly, in situ formed carbon could be introduced into the product (i.e., Fe{sub 2}O{sub 3}/C nano-composites) by simply increasing the dosage of citric acid in the precursor solution. The as-prepared Fe{sub 2}O{sub 3}/C nano-composite exhibited high reversible capacities of 470 and 419 mA h g{sup −1} at the 80th and 200th cycles with a current density of 125 mA g{sup −1}, which are much higher than those of counterparts without carbon (i.e., Fe{sub 2}O{sub 3} nano-particles). Comparison experiments correlated with the performance improvement of Fe{sub 2}O{sub 3}/C nano-composites with in situ formed carbon, well-developed mesopores and relatively high specific surface areas.

  4. Progress in Graphene and its Composites as Anode Material for Lithium-ion Battery%石墨烯及其复合材料作为锂离子电池负极材料的研究进展

    Institute of Scientific and Technical Information of China (English)

    赵阳; 黄英; 王秋芬; 王潇雅; 宗蒙; 何倩

    2012-01-01

    Graphene as the lithium-ion battery anode material shows excellent electrochemical performance. In this paper, the research of the anode-material of graphene, the metal/graphene composites, metal-oxide/graphene composites and other composites of grapheme were introduced. The advantge of graphene-anode material and the application prospects of graphene-based composite materials in lithium-ion battery anode materials are described.%石墨烯作为一种锂离子电池负极材料表现出优异的电化学性能.本文介绍了石墨烯负极材料、金属/石墨烯复合材料、金属氧化物/石墨烯复合材料和其他石墨烯复合材料的研究现状,阐述了石墨烯作为负极材料的优越性,展望了石墨烯及其复合复合材料在锂离子电池负极材料中的应用前景.

  5. Bio-inspired 2-line ferrihydrite as a high-capacity and high-rate-capability anode material for lithium-ion batteries

    Science.gov (United States)

    Hashimoto, Hideki; Ukita, Masahiro; Sakuma, Ryo; Nakanishi, Makoto; Fujii, Tatsuo; Imanishi, Nobuyuki; Takada, Jun

    2016-10-01

    A high-capacity and high-rate-capability anode material for lithium-ion batteries, silicon-doped iron oxyhydroxide or 2-line ferrihydrite (2Fh), was prepared by mixing iron nitrate powder, tetraethyl orthosilicate, 2-propanol, and ammonium hydrogen carbonate powder at room temperature. The design of this material was inspired by a bacteriogenic product, a nanometric amorphous iron-based oxide material containing small amounts of structural Si. The atomistic structure of the prepared Si-doped 2Fh was strongly affected by the Si molar ratio [x = Si/(Fe + Si)]. Its crystallinity gradually decreased as the Si molar ratio increased, with a structural variation from nanocrystalline to amorphous at x = 0.25. The sample with x = 0.20 demonstrated the best Li storage performance. The developed material exhibited a high capacity of ∼400 mAh g-1 at the 25th cycle in the voltage range of 0.3-3.0 V and at a current rate of 9 A g-1, which was three times greater than that of the Si-free 2Fh. This indicates that Si-doping into the 2Fh structure realizes good rate capability, which are presumably because of the specific nanocomposite structure of iron-based electrochemical centers embedded in the Si-based amorphous matrix, generated by reversible Li insertion/deinsertion process.

  6. Anatase TiO2@C composites with porous structure as an advanced anode material for Na ion batteries

    Science.gov (United States)

    Shi, Xiaodong; Zhang, Zhian; Du, Ke; Lai, Yanqing; Fang, Jing; Li, Jie

    2016-10-01

    In this paper, we propose a facile strategy to synthesize the porous structure TiO2@C composites through a two-step method, in which the precursor of MIL-125(Ti) was firstly prepared by solvent thermal method and then calcined under inert atmosphere. When employed as anodes for Na ion batteries, TiO2@C composites can exhibit a superior cyclability with a reversible sodium storage capacity of 148 mAh g-1 at the current density 0.5 A g-1 after 500 cycles and an excellent rate performance with a capacity of 88.9 mAh g-1 even the current reached to 2.5 A g-1 due to the dispersion of anatase TiO2 throughout amorphous carbon matrix and the synergistic effect between the anatase TiO2 nanocrystals and carbon matrix, which can availably enhance the electric conductivity and alleviate the volumetric variation of TiO2 during the insertion/extraction process of Na+.

  7. Hard carbon nanoparticles as high-capacity, high-stability anodic materials for Na-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Xiao, Lifen; Cao, Yuliang; Henderson, Wesley A.; Sushko, Maria L.; Shao, Yuyan; Xiao, Jie; Wang, Wei; Engelhard, Mark H.; Nie, Zimin; Liu, Jun

    2016-01-01

    Hard carbon nanoparticles (HCNP) were synthesized by the pyrolysis of a polyaniline precursor. The measured Na+ cation diffusion coefficient (10-13-10-15cm2s-1) in the HCNP obtained at 1150 °C is two orders of magnitude lower than that of Li+ in graphite (10-10-13-15cm2s-1), indicating that reducing the carbon particle size is very important for improving electrochemical performance. These measurements also enable a clear visualization of the stepwise reaction phases and rate changes which occur throughout the insertion/extraction processes in HCNP, The electrochemical measurements also show that the nano-sized HCNP obtained at 1150 °C exhibited higher practical capacity at voltages lower than 1.2 V (vs. Na/Na⁺), as well as a prolonged cycling stability, which is attributed to an optimum spacing of 0.366 nm between the graphitic layers and the nano particular size resulting in a low-barrier Na+ cation insertion. These results suggest that HCNP is a very promising high-capacity/stability anode for low cost sodium-ion batteries (SIBs).

  8. Synthesis of Mesoporous ZnO Nanosheets via Facile Solvothermal Method as the Anode Materials for Lithium-ion Batteries.

    Science.gov (United States)

    Wang, Xin; Huang, Lanyan; Zhao, Yan; Zhang, Yongguang; Zhou, Guofu

    2016-12-01

    Mesoporous ZnO nanosheets are synthesized through a room temperature solvothermal method. Transmission and scanning electronic microscopy observations indicate that as-prepared ZnO hierarchical aggregates are composed and assembled by nanosheets with a length of 1-2 μm and a thickness of 10-20 nm, and interlaced ZnO nanosheets irregularly stack together, forming a three-dimensional network. Furthermore, large mesopores are embedded in the walls of ZnO nanosheets, confirmed by Brunauer-Emmett-Teller (BET) measurement. Accordingly, the resulting ZnO anode exhibits a high and stable specific discharge capacity of 421 mAh g(-1) after 100 cycles at 200 mA g(-1) and a good rate capability. Such electrochemical performance could be attributed to the multiple synergistic effects of its mesoporous nanosheet structure, which can not only provide a large specific surface area for lithium storage, but also favor the ion transport and electrolyte diffusion. PMID:26815606

  9. Raw data for neutron scattering experiments described in PhD thesis "NMR and neutron total scattering studies of silicon-based anode materials for lithium-ion batteries"

    OpenAIRE

    Kerr, Christopher J

    2014-01-01

    The research focuses on the structural transformations in silicon and lithium silicides during the electrochemical reactions that occur when using silicon as an anode material for lithium-ion batteries. This dataset contains raw neutron-scattering data, as well as battery charger log files showing the electrical performance of the batteries. Results of the data processing will be uploaded to a separate dataset.

  10. Chemo-mechanical softening during in situ nanoindentation of anodic porous alumina with anodization processing

    OpenAIRE

    Cheng, C; Ngan, AHW

    2013-01-01

    Simultaneous application of mechanical stresses on a material as it undergoes an electrochemical reaction can result in interesting coupling effects between the chemical and mechanical responses of the material. In this work, anodic porous alumina supported on Al is found to exhibit significant softening during in situ nanoindentation with anodization processing. Compared with ex situ nanoindentation without anodization processing, the in situ hardness measured on the alumina is found to be m...

  11. Unique Urchin-like Ca2Ge7O16 Hierarchical Hollow Microspheres as Anode Material for the Lithium Ion Battery

    Science.gov (United States)

    Li, Dan; Feng, Chuanqi; Liu, Hua Kun; Guo, Zaiping

    2015-06-01

    Germanium is an outstanding anode material in terms of electrochemical performance, especially rate capability, but its developments are hindered by its high price because it is rare in the crust of earth, and its huge volume variation during the lithium insertion and extraction. Introducing other cheaper elements into the germanium-based material is an efficient way to dilute the high price, but normally sacrifice its electrochemical performance. By the combination of nanostructure design and cheap element (calcium) introduction, urchin-like Ca2Ge7O16 hierarchical hollow microspheres have been successfully developed in order to reduce the price and maintain the good electrochemical properties of germanium-based material. The electrochemical test results in different electrolytes show that ethylene carbonate/dimethyl carbonate/diethyl carbonate (3/4/3 by volume) with 5 wt% fluoroethylene carbonate additive is the most suitable solvent for the electrolyte. From the electrochemical evaluation, the as-synthesized Ca2Ge7O16 hollow microspheres exhibit high reversible specific capacity of up to 804.6 mA h g-1 at a current density of 100 mA g-1 after 100 cycles and remarkable rate capability of 341.3 mA h g-1 at a current density of 4 A g-1. The growth mechanism is proposed based on our experimental results on the growth process.

  12. Unique Urchin-like Ca2Ge7O16 Hierarchical Hollow Microspheres as Anode Material for the Lithium Ion Battery.

    Science.gov (United States)

    Li, Dan; Feng, Chuanqi; Liu, Hua Kun; Guo, Zaiping

    2015-01-01

    Germanium is an outstanding anode material in terms of electrochemical performance, especially rate capability, but its developments are hindered by its high price because it is rare in the crust of earth, and its huge volume variation during the lithium insertion and extraction. Introducing other cheaper elements into the germanium-based material is an efficient way to dilute the high price, but normally sacrifice its electrochemical performance. By the combination of nanostructure design and cheap element (calcium) introduction, urchin-like Ca2Ge7O16 hierarchical hollow microspheres have been successfully developed in order to reduce the price and maintain the good electrochemical properties of germanium-based material. The electrochemical test results in different electrolytes show that ethylene carbonate/dimethyl carbonate/diethyl carbonate (3/4/3 by volume) with 5 wt% fluoroethylene carbonate additive is the most suitable solvent for the electrolyte. From the electrochemical evaluation, the as-synthesized Ca2Ge7O16 hollow microspheres exhibit high reversible specific capacity of up to 804.6 mA h g(-1) at a current density of 100 mA g(-1) after 100 cycles and remarkable rate capability of 341.3 mA h g(-1) at a current density of 4 A g(-1). The growth mechanism is proposed based on our experimental results on the growth process.

  13. Unique Urchin-like Ca2Ge7O16 Hierarchical Hollow Microspheres as Anode Material for the Lithium Ion Battery.

    Science.gov (United States)

    Li, Dan; Feng, Chuanqi; Liu, Hua Kun; Guo, Zaiping

    2015-01-01

    Germanium is an outstanding anode material in terms of electrochemical performance, especially rate capability, but its developments are hindered by its high price because it is rare in the crust of earth, and its huge volume variation during the lithium insertion and extraction. Introducing other cheaper elements into the germanium-based material is an efficient way to dilute the high price, but normally sacrifice its electrochemical performance. By the combination of nanostructure design and cheap element (calcium) introduction, urchin-like Ca2Ge7O16 hierarchical hollow microspheres have been successfully developed in order to reduce the price and maintain the good electrochemical properties of germanium-based material. The electrochemical test results in different electrolytes show that ethylene carbonate/dimethyl carbonate/diethyl carbonate (3/4/3 by volume) with 5 wt% fluoroethylene carbonate additive is the most suitable solvent for the electrolyte. From the electrochemical evaluation, the as-synthesized Ca2Ge7O16 hollow microspheres exhibit high reversible specific capacity of up to 804.6 mA h g(-1) at a current density of 100 mA g(-1) after 100 cycles and remarkable rate capability of 341.3 mA h g(-1) at a current density of 4 A g(-1). The growth mechanism is proposed based on our experimental results on the growth process. PMID:26061390

  14. Morphology-controlled synthesis and electrochemical performance of NiCo2O4 as anode material in lithium-ion battery application

    International Nuclear Information System (INIS)

    Mixed-valence oxide precursors were synthesized by a solvothermal method using NiSO4, CoSO4, and NH4HCO3 as raw materials. The precursors were heat-treated in a muffle furnace at 500 °C to obtain the products (NiCo2O4). The samples were characterized by X-ray diffractometer, thermogravimetric, energy-dispersive spectroscopy, scanning electron microscopy, and transmission electron microscopy. The results show that dumbbells, microspheres, and particle-like NiCo2O4 were successfully synthesized by changing the volume of solvent and solvothermal temperature. The NiCo2O4 microspheres (prepared at 180 °C with 30 ml solvent) as anode material for lithium-ion battery, exhibit a reversible discharge capacity of 1160 mAh g−1 and good cycling stability (729 mAh g−1 after 50 cycles) at a constant current of 100 mA g−1 in the voltage range of 0.01–3.0 V due to its high crystallinity and uniform porous morphology. Hence, the synthetic method could be extended to other high-capacity ternary metal oxide materials for lithium-ion battery application

  15. Morphology-controlled synthesis and electrochemical performance of NiCo{sub 2}O{sub 4} as anode material in lithium-ion battery application

    Energy Technology Data Exchange (ETDEWEB)

    Xu, Shan; Lu, Lin; Zhang, Qing; Zheng, Hao; Liu, Lian; Yin, Shengyu; Wang, Shiquan, E-mail: wsqhao@126.com; Li, Guohua; Feng, Chuanqi [Hubei University, Hubei Collaborative Innovation Center for Advanced Organic Chemical Materials, Ministry-of-Education Key Laboratory for Synthesis and Applications of Organic Functional Molecules (China)

    2015-09-15

    Mixed-valence oxide precursors were synthesized by a solvothermal method using NiSO{sub 4}, CoSO{sub 4}, and NH{sub 4}HCO{sub 3} as raw materials. The precursors were heat-treated in a muffle furnace at 500 °C to obtain the products (NiCo{sub 2}O{sub 4}). The samples were characterized by X-ray diffractometer, thermogravimetric, energy-dispersive spectroscopy, scanning electron microscopy, and transmission electron microscopy. The results show that dumbbells, microspheres, and particle-like NiCo{sub 2}O{sub 4} were successfully synthesized by changing the volume of solvent and solvothermal temperature. The NiCo{sub 2}O{sub 4} microspheres (prepared at 180 °C with 30 ml solvent) as anode material for lithium-ion battery, exhibit a reversible discharge capacity of 1160 mAh g{sup −1} and good cycling stability (729 mAh g{sup −1} after 50 cycles) at a constant current of 100 mA g{sup −1} in the voltage range of 0.01–3.0 V due to its high crystallinity and uniform porous morphology. Hence, the synthetic method could be extended to other high-capacity ternary metal oxide materials for lithium-ion battery application.

  16. Alkali-Metal-Ion-Functionalized Graphene Oxide as a Superior Anode Material for Sodium-Ion Batteries.

    Science.gov (United States)

    Wan, Fang; Li, Yu-Han; Liu, Dai-Huo; Guo, Jin-Zhi; Sun, Hai-Zhu; Zhang, Jing-Ping; Wu, Xing-Long

    2016-06-01

    Although graphene oxide (GO) has large interlayer spacing, it is still inappropriate to use it as an anode for sodium-ion batteries (SIBs) because of the existence of H-bonding between the layers and ultralow electrical conductivity which impedes the Na(+) and e(-) transformation. To solve these issues, chemical, thermal, and electrochemical procedures are traditionally employed to reduce GO nanosheets. However, these strategies are still unscalable, consume high amounts of energy, and are expensive for practical application. Here, for the first time, we describe the superior Na storage of unreduced GO by a simple and scalable alkali-metal-ion (Li(+) , Na(+) , K(+) )-functionalized process. The various alkali metals ions, connecting with the oxygen on GO, have played different effects on morphology, porosity, degree of disorder, and electrical conductivity, which are crucial for Na-storage capabilities. Electrochemical tests demonstrated that sodium-ion-functionalized GO (GNa) has shown outstanding Na-storage performance in terms of excellent rate capability and long-term cycle life (110 mAh g(-1) after 600 cycles at 1 A g(-1) ) owing to its high BET area, appropriate mesopore, high degree of disorder, and improved electrical conductivity. Theoretical calculations were performed using the generalized gradient approximation (GGA) to further study the Na-storage capabilities of functionalized GO. These calculations have indicated that the Na-O bond has the lowest binding energy, which is beneficial to insertion/extraction of the sodium ion, hence the GNa has shown the best Na-storage properties among all comparatives functionalized by other alkali metal ions. PMID:27136376

  17. Characteristics and Electrochemical Performance of Si-Carbon Nanofibers Composite as Anode Material for Binder-Free Lithium Secondary Batteries.

    Science.gov (United States)

    Hyun, Yura; Park, Heai-Ku; Park, Ho-Seon; Lee, Chang-Seop

    2015-11-01

    The carbon nanofibers (CNFs) and Si-CNFs composite were synthesized using a chemical vapor deposition (CVD) method with an iron-copper catalyst and silicon-covered Ni foam. Acetylene as a carbon source was flowed into the quartz reactor of a tubular furnace heated to 600 degrees C. This temperature was maintained for 10 min to synthesize the CNFs. The morphologies, compositions, and crystal quality of the prepared CNFs were characterized by Scanning electron microscopy (SEM), Energy dispersive spectroscopy (EDS), X-ray Diffraction (XRD), Raman spectroscopy, and X-ray photoelectron spectroscopy (XPS). The electrochemical characteristics of the Si-CNFs composite as an anode of the Li secondary batteries were investigated using a three-electrode cell. The as-deposited Si-CNF composite on the Ni foam was directly employed as an working electrode without any binder, and lithium foil was used as the counter and reference electrode. A glass fiber separator was used as the separator membrane. Two kinds of electrolytes were employed; 1) 1 M LiPF6 was dissolved in a mixture of EC (ethylene carbonate): PC (propylene carbonate): EMC (Ethyl methyl carbonate) in a 1:1:1 volume ratio and 2) 1 M LiClO4 was dissolved in a mixture of propylene carbonate (PC): ethylene carbonate (EC) in a 1:1 volume ratio. The galvanostatic charge-discharge cycling and cyclic voltammetry measurements were carried out at room temperature by using a battery tester. The resulting Si-CNFs composite achieved the large discharge capacity of 613 mAh/g and much improved cycle-ability with the retention rate of 87% after 20 cycles.

  18. Synthesis of TiO2 by electrochemical method from TiCl4 solution as anode material for lithium-ion batteries

    Science.gov (United States)

    Nur, Adrian; Purwanto, Agus; Jumari, Arif; Dyartanti, Endah R.; Sari, Sifa Dian Permata; Hanifah, Ita Nur

    2016-02-01

    Metal oxide combined with graphite becomes interesting composition. TiO2 is a good candidate for Li ion battery anode because of cost, availability of sufficient materials, and environmentally friendly. TiO2 gravimetric capacity varied within a fairly wide range. TiO2 crystals form highly depends on the synthesis method used. The electrochemical method is beginning to emerge as a valuable option for preparing TiO2 powders. Using the electrochemical method, the particle can easily be controlled by simply adjusting the imposed current or potential to the system. In this work, the effects of some key parameters of the electrosynthesis on the formation of TiO2 have been investigated. The combination of graphite and TiO2 particle has also been studied for lithium-ion batteries. The homogeneous solution for the electrosynthesis of TiO2 powders was TiCl4 in ethanol solution. The electrolysis was carried out in an electrochemical cell consisting of two carbon electrodes with dimensions of (5 × 2) cm. The electrodes were set parallel with a distance of 2.6 cm between the electrodes and immersed in the electrolytic solution at a depth of 2 cm. The electrodes were connected to the positive and negative terminals of a DC power supply. The electrosynthesis was performed galvanostatically at 0.5 to 2.5 hours and voltages were varied from 8 to 12 V under constant stirring at room temperature. The resulted suspension was aged at 48 hrs, filtered, dried directly in an oven at 150°C for 2 hrs, washed 2 times, and dried again 60 °C for 6 hrs. The particle product has been used to lithium-ion battery as anode. Synthesis of TiO2 particle by electrochemical method at 10 V for 1 to 2.5 hrs resulted anatase and rutile phase.

  19. Development of mats composed by TiO{sub 2} and carbon dual electrospun nanofibers: A possible anode material in microbial fuel cells

    Energy Technology Data Exchange (ETDEWEB)

    Garcia-Gomez, Nora A.; Balderas-Renteria, Isaias [Universidad Autónoma de Nuevo León, Facultad de Ciencias Químicas, Av. Universidad S/N Cd. Universitaria San Nicolás de los Garza Nuevo León, C.P. 66451 México (Mexico); Garcia-Gutierrez, Domingo I. [Universidad Autónoma de Nuevo León, Facultad de Ingeniería Mecánica y Eléctrica, Av. Universidad S/N Cd. Universitaria San Nicolás de los Garza Nuevo León, C.P. 66451 México (Mexico); Universidad Autónoma de Nuevo León, Centro de Innovación, Investigación y Desarrollo en Ingeniería y Tecnología, PIIT, Av. Universidad S/N Cd. Universitaria San Nicolás de los Garza Nuevo León, C.P. 66451 México (Mexico); Mosqueda, Hugo A. [Universidad Autónoma de Nuevo León, Facultad de Ingeniería Mecánica y Eléctrica, Av. Universidad S/N Cd. Universitaria San Nicolás de los Garza Nuevo León, C.P. 66451 México (Mexico); and others

    2015-03-15

    Highlights: • Dual nanofiber of TiO{sub 2}–C/C showed excellent electrical performance. • TiO{sub 2}–C/C dual nanofiber can host a dense biofilm of electroactivated Escherichia coli. • Dual nanofibers can be applied as anode to obtain electricity in microbial fuel cells. - Abstract: A new material based on TiO{sub 2(rutile)}–C{sub (semi-graphitic)}/C{sub (semi-graphitic)} dual nanofiber mats is presented, whose composition and synthesis methodology are fundamental factors for the development of exoelectrogenic biofilms on its surface. Therefore, this material shows the required characteristics for possible applications in the bioconversion process of an organic substrate to electricity in a microbial fuel cell. Chronoamperometry, cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and electrical conductivity analyses showed excellent electrical performance of the material for the application intended; a resistance as low as 3.149 Ω was able to be measured on this material. Furthermore, scanning electron microscopy (SEM) and transmission electron microscopy (TEM) studies confirmed the morphology sought on the material for the application intended, dual nanofibres TiO{sub 2(rutile)}–C{sub (semi-graphitic)}/C{sub (semi-graphitic)} with a side by side configuration. The difference in composition of the fibers forming the dual nanofibers was clearly observed and confirmed by energy dispersive X-ray spectroscopy (EDXS), and their crystal structure was evident in the results obtained from selected area electron diffraction (SAED) studies. This nanostructured material presented a high surface area and is biocompatible, given that it can host a dense biofilm of electroactivated Escherichia coli. In this study, the maximum current density obtained in a half microbial fuel cell was 8 A/m{sup 2} (0.8 mA/cm{sup 2})

  20. Reactions on carbon anodes in aluminium electrolysis

    Energy Technology Data Exchange (ETDEWEB)

    Eidet, Trygve

    1997-12-31

    The consumption of carbon anodes and energy in aluminium electrolysis is higher than what is required theoretically. This thesis studies the most important of the reactions that consume anode materials. These reactions are the electrochemical anode reaction and the airburn and carboxy reactions. The first part of the thesis deals with the kinetics and mechanism of the electrochemical anode reaction using electrochemical impedance spectroscopy. The second part deals with air and carboxy reactivity of carbon anodes and studies the effects of inorganic impurities on the reactivity of carbon anodes in the aluminium industry. Special attention is given to sulphur since its effect on the carbon gasification is not well understood. Sulphur is always present in anodes, and it is expected that the sulphur content of available anode cokes will increase in the future. It has also been suggested that sulphur poisons catalyzing impurities in the anodes. Other impurities that were investigated are iron, nickel and vanadium, which are common impurities in anodes which have been reported to catalyze carbon gasification. 88 refs., 92 figs., 24 tabs.

  1. Electrochemical properties of CoFe3Sb12 as potential anode material for lithium-ion batteries

    Institute of Scientific and Technical Information of China (English)

    赵新兵; 钟耀东; 曹高劭

    2004-01-01

    A skutterudite-related antimonide, CoFe3Sb12,was prepared with vacuum melting.XRD analysis showed the material contained Sb, FeSb2, CoSb2 and CoSb3 phases.The electrochemical properties of the ball-milled CoFe3Sb12-10wt% graphite composite were studied using pure lithium as the reference electrode. A maximal lithium inserting capacity of about 860 mAh/g was obtained in the first cycle.The reversible capacity of the material was about 560mAh/g in the first cycle and decreased to ca.320 mAh/g and 250 mAh/g after 10 and 20 cycles respectively.Ex-situ XRD analyses showed that the antimonides in the pristine material were decomposed after the first discharge and that antimony was the active element for lithium to insert into the host material.

  2. A facile solution combustion synthesis of nanosized amorphous iron oxide incorporated in a carbon matrix for use as a high-performance lithium ion battery anode material

    Energy Technology Data Exchange (ETDEWEB)

    Zhu, Chunyu, E-mail: chunyu6zhu@gmail.com; Saito, Genki; Akiyama, Tomohiro

    2015-06-05

    Highlights: • Iron oxide–carbon composite was fabricated by facile solution combustion synthesis. • Iron oxide nanoparticles of about 5 nm were uniformly embedded in dense carbon matrix. • The composite exhibited enhanced cyclability and rate capability. • A high capacity of 687 mA h g{sup −1} after 200 cycles at a current rate of 0.5 A g{sup −1} were obtained. - Abstract: An amorphous iron oxide–carbon composite has been fabricated through an effective, inexpensive, and scalable method employing solution combustion synthesis. Amorphous iron oxide nanoparticles with diameters of about 5 nm were synthesized and uniformly embedded in a dense carbon matrix. The synthesized composite exhibits enhanced cyclability and rate capability, showing a high reversible capacity of 687 mA h g{sup −1} after 200 discharge/charge cycles at a current rate of 0.5 A g{sup −1}, compared to the 400 mA h g{sup −1} observed for Fe{sub 2}O{sub 3} nanoparticles. This enhanced performance was retained despite more demanding conditions, delivering a high capacity of about 525 mA h g{sup −1} and a nearly perfect coulombic efficiency even after 400 cycles at 1 A g{sup −1}. The easy production and superior electrochemical properties of this composite suggest that it is a promising material for use as an anode material in high performance lithium ion batteries.

  3. Influence of lithium precursors and calcination atmospheres on graphene sheets-modified nano-Li4Ti5O12 anode material

    Science.gov (United States)

    Li, Wen-Ting; Yuan, Tao; Zhang, Weimin; Ma, Jingjing; Zhang, Chunming; He, Yu-Shi; Liao, Xiao-Zhen; Ma, Zi-Feng

    2015-07-01

    The influence of Li precursors and calcination atmospheres on the reaction mechanisms, physical properties and electrochemical performance of graphene sheets (GS)-modified nano-Li4Ti5O12 (LTO/GS) has been systematically investigated. Field emission scanning electron microscopy (FE-SEM) and mass spectrometry (MS) results demonstrate the lithium precursor containing carboxyl anion such as lithium acetate (LiAc) and Li2CO3 interact with oxygen groups of graphene oxide (GO) by strong hydrogen bonds to restrict the morphology and the phase formation of products. We also notice from the thermogravimetry (TG) and MS results that the consumption of GS is proportional to oxygen content of lithium precursor. Cyclic voltammetry (CV) and X-ray photoelectric spectroscopy (XPS) results indicate that the product calcined in reducing atmosphere possess smaller electrochemical polarization due to more reduced Ti3+ on the surface of the product. The LTO/GS sample with LiOH as Li precursor calcined in diluted hydrogen atmosphere show the best electrochemical performance with a capacity of 134.4 mAh g-1 at 10C discharge rate and very stable cycling life with a 98.6% capacity retention after 800 cycles at 40C rate. This study not only provides an optimization of Li precursor and calcination condition for LTO/GS anode material, but also guides any future one-step syntheses of lithium composite materials with GO participation.

  4. Silicon on conductive self-organized TiO2 nanotubes - A high capacity anode material for Li-ion batteries

    Science.gov (United States)

    Brumbarov, Jassen; Kunze-Liebhäuser, Julia

    2014-07-01

    The study of high energy density electrode materials is central to the development of Li+-ion batteries. Si is among the most promising anode materials for next generation Li+-ion batteries. Model composite electrodes of self-organized, conductive titania (TiO2-x-C) nanotubes coated with silicon (Si) via plasma enhanced chemical vapor deposition (PECVD) are produced and studied in terms of their lithiation/delithiation characteristics. The nanotube array provides direct one dimensional electron transport to the current collector, without the need of adding binders or conductive additives. Both components of the composite can be lithiated delivering 120 μAh cm-2 total capacity for a film thickness of 1 μm and a Si loading of ∼10 wt.%. 86% capacity retention upon 88 cycles at a rate of C/5 and 60 μAh cm-2 total capacity at a rate of 10 C are achieved owing to the low lateral expansion and thus good adhesion of the thin Si coating to the TiO2-x-C nanotubes, and due to the formation of a stable solid electrolyte interface (SEI) in ethylene-carbonate (EC), dimethyl-carbonate (DMC), vinylene-carbonate (VC) electrolyte with 1 M LiPF6.

  5. First Introduction of NiSe2 to Anode Material for Sodium-Ion Batteries: A Hybrid of Graphene-Wrapped NiSe2/C Porous Nanofiber

    Science.gov (United States)

    Cho, Jung Sang; Lee, Seung Yeon; Kang, Yun Chan

    2016-03-01

    The first-ever study of nickel selenide materials as efficient anode materials for Na-ion rechargeable batteries is conducted using the electrospinning process. NiSe2-reduced graphene oxide (rGO)-C composite nanofibers are successfully prepared via electrospinning and a subsequent selenization process. The electrospun nanofibers giving rise to these porous-structured composite nanofibers with optimum amount of amorphous C are obtained from the polystyrene to polyacrylonitrile ratio of 1/4. These composite nanofibers also consist of uniformly distributed single-crystalline NiSe2 nanocrystals that have a mean size of 27 nm. In contrast, the densely structured bare NiSe2 nanofibers formed via selenization of the pure NiO nanofibers consist of large crystallites. The initial discharge capacities of the NiSe2-rGO-C composite and bare NiSe2 nanofibers at a current density of 200 mA g-1 are 717 and 755 mA h g-1, respectively. However, the respective 100th-cycle discharge capacities of the former and latter are 468 and 35 mA h g-1. Electrochemical impedance spectroscopy measurements reveal the structural stability of the composite nanofibers during repeated Na-ion insertion and extraction processes. The excellent Na-ion storage properties of these nanofibers are attributed to this structural stability.

  6. Facile hybridization of Ni@Fe2O3 superparticles with functionalized reduced graphene oxide and its application as anode material in lithium-ion batteries.

    Science.gov (United States)

    Backert, Gregor; Oschmann, Bernd; Tahir, Muhammad Nawaz; Mueller, Franziska; Lieberwirth, Ingo; Balke, Benjamin; Tremel, Wolfgang; Passerini, Stefano; Zentel, Rudolf

    2016-09-15

    In our present work we developed a novel graphene wrapping approach of Ni@Fe2O3 superparticles, which can be extended as a concept approach for other nanomaterials as well. It uses sulfonated reduced graphene oxide, but avoids thermal treatments and use of toxic agents like hydrazine for its reduction. The modification of graphene oxide is achieved by the introduction of sulfate groups accompanied with reduction and elimination reactions, due to the treatment with oleum. The successful wrapping of nanoparticles is proven by energy dispersive X-ray spectroscopy, high-resolution transmission electron microscopy and Raman spectroscopy. The developed composite material shows strongly improved performance as anode material in lithium-ion batteries (compared to unwrapped Ni@Fe2O3) as it offers a reversible capacity of 1051mAhg(-1) after 40 cycles at C/20, compared with 460mAhg(-1) for unwrapped Ni@Fe2O3. The C rate capability is also improved by the wrapping approach, as specific capacities for wrapped particles are about twice of those offered by unwrapped particles. Additionally, the benefit for the use of the advanced superparticle morphology is demonstrated by comparing wrapped Ni@Fe2O3 particles with wrapped Fe2O3 nanorice.

  7. Development of anode material based on La-substituted SrTiO{sub 3} perovskites doped with manganese and/or gallium for SOFC

    Energy Technology Data Exchange (ETDEWEB)

    Escudero, M.J. [Dpto Energia, CIEMAT, Av. Complutense 22, 28040 Madrid (Spain); School of Chemistry, Purdie Building, University of St Andrews, St Andres, Fife KY16 9ST (United Kingdom); Irvine, J.T.S. [School of Chemistry, Purdie Building, University of St Andrews, St Andres, Fife KY16 9ST (United Kingdom); Daza, L. [Dpto Energia, CIEMAT, Av. Complutense 22, 28040 Madrid (Spain); Instituto de Catalisis y Petroleoquimica (CSIC), Campus Cantoblanco, C/Marie Curie 2, 28049 Madrid (Spain)

    2009-07-01

    Materials based on La-substituted SrTiO{sub 3} perovskites doped with manganese and/or gallium for SOFC have been studied as novel anodes for solid oxide fuel cell. La{sub 4}Sr{sub 8}Ti{sub 11}Mn{sub 1-x}Ga{sub x}O{sub 38-{delta}} (0 {<=} x {<=} 1) oxides were synthesized by solid state reaction and the influences of the manganese and/or gallium content on the structure, morphology, thermal properties and electrical conductivity of these materials has been investigated. All compounds show cubic structure with a space group Pm-3m. These compounds presented high electrical conductivity values under reducing atmosphere between 7.9 and 6.8 S cm{sup -1} at 900 C. For the composition x {>=} 0.5, the thermal expansion coefficient in both reducing and oxidizing atmosphere are close to that of SOFC electrolytes (8YSZ, CGD). In general, the substitution of Ga by Mn causes a slight reduction in each of the following, lattice parameter, degree of oxygen loss on reduction, thermal expansion coefficient, and electrical conductivity. (author)

  8. Rational design of mixed ionic and electronic conducting perovskite oxides for solid oxide fuel cell anode materials: A case study for doped SrTiO3

    Energy Technology Data Exchange (ETDEWEB)

    Suthirakun, Suwit; Xiao, Guoliang; Ammal, Salai Cheettu; Chen, Fanglin; zur Loye, Hans-Conrad; Heyden, Andreas

    2014-01-01

    The effect of p- and n-type dopants on ionic and electronic conductivity of SrTiO3 based perovskites were investigated both computationally and experimentally. Specifically, we performed density functional theory (DFT) calculations of Na- and La-doped SrTiO3 and Na- and Nb-doped SrTiO3 systems. Constrained ab initio thermodynamic calculations were used to evaluate the phase stability and reducibility of doped SrTiO3 under both oxidizing and reducing synthesis conditions, as well as under anodic solid oxide fuel cell (SOFC) conditions. The density of states (DOS) of these materials was analyzed to study the effects of p- and n-doping on the electronic conductivity. Furthermore, Na- and La-doped SrTiO3 and Na- and Nb-doped SrTiO3 samples were experimentally prepared and the conductivity was measured to confirm our computational predictions. The experimental observations are in very good agreement with the theoretical predictions that doping n-doped SrTiO3 with small amounts of p-type dopants promotes both the ionic and electronic conductivity of the material. This doping strategy is valid independent of p- and n-doping site and permits the synthesis of perovskite based mixed ionic/electronic conductors.

  9. Influence of Sc3+ doping in B-site on electrochemical performance of Li4Ti5O12 anode materials for lithium-ion battery

    Science.gov (United States)

    Zhang, Yaoyao; Zhang, Chunming; Lin, Ye; Xiong, Ding-Bang; Wang, Dan; Wu, Xiaoyan; He, Dannong

    2014-03-01

    Anode materials Li4Ti5O12 (LTO) and Sc-doped Li4Ti4.95Sc0.05O12-δ (LTSO) for lithium-ion batteries are both successfully synthesized by the modified sol-gel method with ethylene diamine tetraacetic acid (EDTA) and citric acid (CA) as a bi-components chelating agent. The samples are characterized by XRD, BET, XPS, EDX and SEM. The dopant Sc totally enters into the 16d sites of the spinel structure of LTO, and then further affects its morphology and property. The LTSO powder exhibits a 3D network morphology and its grain size is about 200 nm. The LTSO electrode material exhibits an excellent initial discharge capacities of 174 and 94 mAh g-1 at 1 C and 40 C, respectively. The reversible capacities of LTSO at different current rates remain nearly 100% after 50 cycles, which are compared with the capacities of the second cycles. Sc3+ doping can greatly improve the electronic conductivity of LTO which is demonstrated by electrochemical impedance spectroscopy. Cyclic voltammetry measurements also reveal that LTSO has small polarization resistance due to the high electrical conductivity and Li-ion apparent diffusion rate.

  10. Nanoparticulate Mn3O4/VGCF composite conversion-anode material with extraordinarily high capacity and excellent rate capability for lithium ion batteries.

    Science.gov (United States)

    Ma, Feng; Yuan, Anbao; Xu, Jiaqiang

    2014-10-22

    In this work, highly conductive vapor grown carbon fiber (VGCF) was applied as an electrically conductive agent for facile synthesis of a nanoparticulate Mn3O4/VGCF composite material. This material exhibits super high specific capacity and excellent rate capability as a conversion-anode for lithium ion batteries. Rate performance test result demonstrates that at the discharge/charge current density of 0.2 A g(-1) a reversible capacity of ca. 950 mAh g(-1) is delivered, and when the current rate is increased to a high current density of 5 A g(-1), a reversible capacity of ca. 390 mAh g(-1) is retained. Cyclic performance examination conducted at the current density of 0.5 A g(-1) reveals that in the initial 20 cycles the reversible capacity decreases gradually from 855 to 747 mAh g(-1). However, since then, it increases gradually with cycle number increasing, and after 200 cycles an extraordinarily high reversible capacity of 1391 mAh g(-1) is achieved.

  11. Facile hybridization of Ni@Fe2O3 superparticles with functionalized reduced graphene oxide and its application as anode material in lithium-ion batteries.

    Science.gov (United States)

    Backert, Gregor; Oschmann, Bernd; Tahir, Muhammad Nawaz; Mueller, Franziska; Lieberwirth, Ingo; Balke, Benjamin; Tremel, Wolfgang; Passerini, Stefano; Zentel, Rudolf

    2016-09-15

    In our present work we developed a novel graphene wrapping approach of Ni@Fe2O3 superparticles, which can be extended as a concept approach for other nanomaterials as well. It uses sulfonated reduced graphene oxide, but avoids thermal treatments and use of toxic agents like hydrazine for its reduction. The modification of graphene oxide is achieved by the introduction of sulfate groups accompanied with reduction and elimination reactions, due to the treatment with oleum. The successful wrapping of nanoparticles is proven by energy dispersive X-ray spectroscopy, high-resolution transmission electron microscopy and Raman spectroscopy. The developed composite material shows strongly improved performance as anode material in lithium-ion batteries (compared to unwrapped Ni@Fe2O3) as it offers a reversible capacity of 1051mAhg(-1) after 40 cycles at C/20, compared with 460mAhg(-1) for unwrapped Ni@Fe2O3. The C rate capability is also improved by the wrapping approach, as specific capacities for wrapped particles are about twice of those offered by unwrapped particles. Additionally, the benefit for the use of the advanced superparticle morphology is demonstrated by comparing wrapped Ni@Fe2O3 particles with wrapped Fe2O3 nanorice. PMID:27295319

  12. One-Pot Synthesis of CoSex -rGO Composite Powders by Spray Pyrolysis and Their Application as Anode Material for Sodium-Ion Batteries.

    Science.gov (United States)

    Park, Gi Dae; Kang, Yun Chan

    2016-03-14

    A simple one-pot synthesis of metal selenide/reduced graphene oxide (rGO) composite powders for application as anode materials in sodium-ion batteries was developed. The detailed mechanism of formation of the CoSe(x)-rGO composite powders that were selected as the first target material in the spray pyrolysis process was studied. The crumple-structured CoSe(x)-rGO composite powders prepared by spray pyrolysis at 800 °C had a crystal structure consisting mainly of Co0.85 Se with a minor phase of CoSe2. The bare CoSe(x) powders prepared for comparison had a spherical shape and hollow structure. The discharge capacities of the CoSe(x)-rGO composite and bare CoSe(x) powders in the 50th cycle at a constant current density of 0.3 A g(-1) were 420 and 215 mA h g(-1), respectively, and their capacity retentions measured from the second cycle were 80 and 46%, respectively. The high structural stability of the CoSe(x)-rGO composite powders for repeated sodium-ion charge and discharge processes resulted in superior sodium-ion storage properties compared to those of the bare CoSe(x) powders. PMID:26864320

  13. Carbon-Rich Silicon Oxycarbide (SiOC) and Silicon Oxycarbide/Element (SiOC/X, X= Si, Sn) Nano-Composites as New Anode Materials for Li-Ion Battery Application

    OpenAIRE

    Kaspar, Jan

    2014-01-01

    Carbon-rich silicon oxycarbide (SiOC) and silicon oxycarbide/element nano-composites (SiOC/X, X=Si, Sn) are prepared via thermal conversion of polyorganosiloxanes and studied as potential anode material for Li-ion battery application. The obtained materials are characterized by various chemical, structural, electrochemical and electro-analytical methods. The chemical composition and microstructure of the samples is analyzed and correlated with their electrochemical properties and performance....

  14. NASICON-Structured NaTi2(PO4)3@C Nanocomposite as the Low Operation-Voltage Anode Material for High-Performance Sodium-Ion Batteries.

    Science.gov (United States)

    Wang, Dongxue; Liu, Qiang; Chen, Chaoji; Li, Malin; Meng, Xing; Bie, Xiaofei; Wei, Yingjin; Huang, Yunhui; Du, Fei; Wang, Chunzhong; Chen, Gang

    2016-01-27

    NASICON-type structured NaTi2(PO4)3 (NTP) has attracted wide attention as a promising anode material for sodium-ion batteries (SIBs), whereas it still suffer from poor rate capability and cycle stability due to the low electronic conductivity. Herein, the architecture, NTP nanoparticles embedded in the mesoporous carbon matrix, is designed and realized by a facile sol-gel method. Different than the commonly employed potentials of 1.5-3.0 V, the Na(+) storage performance is examined at low operation voltages between 0.01 and 3.0 V. The electrode demonstrates an improved capacity of 208 mAh g(-1), one of the highest capacities in the state-of-the-art titanium-based anode materials. Besides the high working plateau at 2.1 V, another one is observed at approximately 0.4 V for the first time due to further reduction of Ti(3+) to Ti(2+). Remarkably, the anode exhibits superior rate capability, whose capacity and corresponding capacity retention reach 56 mAh g(-1) and 68%, respectively, over 10000 cycles under the high current density of 20 C rate (4 A g(-1)). Worthy of note is that the electrode shows negligible capacity loss as the current densities increase from 50 to 100 C, which enables NTP@C nanocomposite as the prospective anode of SIBs with ultrahigh power density. PMID:26720111

  15. A redox-stable direct-methane solid oxide fuel cell (SOFC) with Sr2FeNb0.2Mo0.8O6-δ double perovskite as anode material

    Science.gov (United States)

    Ding, Hanping; Tao, Zetian; Liu, Shun; Yang, Yating

    2016-09-01

    Development of high-performing and redox-stable ceramic oxide electrode materials is a crucial technical step for direct hydrocarbon solid oxide fuel cells (SOFCs) operating at intermediate temperatures (550-700 °C). Here we report a nickel-free double perovskite, Sr2FeNb0.2Mo0.8O6-δ (SFNM20), for SOFC anode, and this anode shows outstanding performances with high resistance against carbon build-up and redox cycling in hydrocarbon fuels. At 800 °C, the SFNM20 anode shows electrical conductivity of 5.3 S cm-1 in 5% H2 and peak power densities of 520 and 380 mW cm-2 using H2 and CH4 as the fuel, respectively. The cell exhibits a very stable performance under different constant current loads in H2 and CH4 at 700 °C and high redox stability against the gas environment changes in the anode chamber. In addition, the electrode is structurally stable in various fuels, suggesting that it is a feasible material candidate for the electrode of high-performing SOFCs.

  16. Effect of the Side Chains and Anode Material on Thermal Stability and Performance of Bulk-Heterojunction Solar Cells Using DPP(TBFu2 Derivatives as Donor Materials

    Directory of Open Access Journals (Sweden)

    Alexander Kovalenko

    2015-01-01

    Full Text Available An optimized fabrication of bulk-heterojunction solar cells (BHJ SCs based on previously reported diketopyrrolopyrrole donor, ethyl-hexylated DPP(TBFu2, as well as two new DPP(TBFu2 derivatives with ethyl-hexyl acetate and diethyl acetal solubilizing side-chains and PC60BM as an acceptor is demonstrated. Slow gradual annealing of the solar cell causing the effective donor-acceptor reorganization, and as a result higher power conversion efficiency (PCE, is described. By replacing a hole transporting layer PEDOT:PSS with MoO3 we obtained higher PCE values as well as higher thermal stability of the anode contact interface. DPP(TBFu2 derivative containing ethyl-hexyl acetate solubilizing side-chains possessed the best as-cast self-assembly and high crystallinity. However, the presence of ethyl-hexyl acetate and diethyl acetal electrophilic side-chains stabilizes HOMO energy of isolated DPP(TBFu2 donors with respect to the ethyl-hexylated one, according to cyclic voltammetry.

  17. MoO2-ordered mesoporous carbon hybrids as anode materials with highly improved rate capability and reversible capacity for lithium-ion battery.

    Science.gov (United States)

    Chen, Ailian; Li, Caixia; Tang, Rui; Yin, Longwei; Qi, Yongxin

    2013-08-28

    A novel hybrid of MoO2-ordered mesoporous carbon (MoO2-OMC) was prepared through a two-step solvothermal chemical reaction route. The electrochemical performances of the mesoporous MoO2-OMC hybrids were examined using galvanostatical charge-discharge, cyclic voltammetry, and electrochemical impedance spectroscopy (EIS) techniques. The MoO2-OMC hybrid exhibits significantly improved electrochemical performance of high reversible capacity, high-rate capability, and excellent cycling performance as an anode electrode material for Li ion batteries. It is revealed that the MoO2-OMC hybrid could deliver the first discharge capacity of 1641.8 mA h g(-1) with an initial Coulombic efficiency of 63.6%, and a reversible capacity as high as 1049.1 mA h g(-1) even after 50 cycles at a current density of 100 mA g(-1), much higher than the theoretical capacity of MoO2 (838 mA h g(-1)) and OMC materials. The MoO2-OMC hybrid demonstrates an excellent high rate capability with capacity of ∼600 mA h g(-1) even at a charge current density of 1600 mA g(-1) after 50 cycles, which is approximately 11.1 times higher than that of the OMC (54 mA h g(-1)) materials. The improved rate capability and reversible capacity of the MoO2-OMC hybrid are attributed to a synergistic reaction between the MoO2 nanoparticles and mesoporous OMC matrices. It is noted that the electrochemical performance of the MoO2-OMC hybrid is evidently much better than the previous MoO2-based hybrids.

  18. Improved electrochemical performance of Ag-modified Li4Ti5O12 anode material in a broad voltage window

    Indian Academy of Sciences (India)

    Yan-Rong Zhu; Ting-Feng Yi; Hong-Tao Ma; Yong-Quan Ma; Li-Juan Jiang; Rong-Sun Zhu

    2014-01-01

    Li4Ti5O12/Ag composites were synthesized by a solid-state method. The effect of Ag modification on the physical and electrochemical properties is discussed by the characterizations of X-ray diffraction, scanning electron microscopy, cyclic voltammetry, electrochemical impedance spectroscopy, cycling and rate tests. The lattice parameter of Li4Ti5O12 with a low Ag content is almost not changed, but the lattice parameter becomes larger due to the high content of Ag. Li4Ti5O12/Ag material has a uniform particle size which is about 1 m. Modification of appropriate Ag is beneficial to the reversible intercalation and deintercalation of Li+. Modification of Ag not only decreases the charge transfer resistance of Li4Ti5O12 material, but also improves the diffusion coefficient of lithium ion. Li4Ti5O12/Ag (3 mass%) material has the lowest charge transfer resistance, the highest diffusion coefficient of lithium ion and the best rate cycling performance.

  19. Studies of Nano-sized Co3O4 as Anode Materials for Lithium-ion Batteries

    Institute of Scientific and Technical Information of China (English)

    HUANG, Fenga; ZHAN, Hui; ZHOU, Yun-Hong

    2003-01-01

    The structural evolution of the Co3O4 fine powders prepared by rheological phase reaction and pyrolysis method upon different temperature has been investigated using X-ray diffraction (XRD) topography. The electrochemical performance of Co3O4electrode materials for Li-ion batteries is studied in the form of Li/Co3O4 cells. The reversible capacity as high as 930 mAh/g for the Co3O4 sample heat-treated at 600 C is achieved and sustained over 30 times charge-discharge cycles at room temperature. The detailed information concerning the reaction mechanism of Co3O4 active material together with lithium ion is obtained through ex-situ XRD topography, X-ray photoelectron spectroscopy (XPS) analysis and cyclic voltammetry (CV) technique. And it is revealed that a "two-step" reaction is involved in the charge and discharge of the Li/Co3O4 cells, in which Co3O4 active material is reversibly reduced into xCo·(3 - x )CoO and then into metallic Co.

  20. Mesoporous MFe{sub 2}O{sub 4} (M = Mn, Co, and Ni) for anode materials of lithium-ion batteries: Synthesis and electrochemical properties

    Energy Technology Data Exchange (ETDEWEB)

    Duan, Lianfeng, E-mail: duanlf@mail.ccut.edu.cn [State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022 (China); Key Laboratory of Advanced Structural Materials, Ministry of Education, and Department of Materials Science and Engineering, Changchun University of Technology, Changchun 130012 (China); Wang, Yuanxin; Wang, Linan [Key Laboratory of Advanced Structural Materials, Ministry of Education, and Department of Materials Science and Engineering, Changchun University of Technology, Changchun 130012 (China); Zhang, Feifei [State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022 (China); University of Chinese Academy of Sciences, Beijing 100049 (China); Wang, Limin [State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022 (China)

    2015-01-15

    Highlights: • MFe{sub 2}O{sub 4} (M = Mn, Co, and Ni) are synthesized by a template-free hydrothermal method. • The mesoporous morphology is formed by self-assembly of crystal nucleus. • The mesporous MnFe{sub 2}O{sub 4} have the active phase and the synergy for Li-ion storage. - Abstract: The MFe{sub 2}O{sub 4} (M = Mn, Co, and Ni) mesoporous spheres with an average diameter of 250 nm were synthesized through a template-free hydrothermal method. The mesoporous MnFe{sub 2}O{sub 4} with a large surface area of 87.5 m{sup 2}/g and an average pore size of 27.52 nm were obtained. As the anode materials for Li-ion batteries, the mesoporous MnFe{sub 2}O{sub 4} exhibits excellent initial charge and discharge capacities of 1010 and 642.5 mA h/g. After 50 cycles, the discharge capacity could still remain at 379 mA h/g. The results showed that the active phase and the synergy between different metal oxides greatly improved the electrochemical performance, and the mesoporous composite could stabilize the structure of the electrodes.

  1. Self-assembled three-dimensional hierarchical NiO nano/microspheres as high-performance anode material for lithium ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Lv, Pengpeng [School of Materials Science and Engineering, University of Science and Technology Beijing, 30 Xueyuan Road, Haidian District, Beijing 100083 (China); Zhao, Hailei, E-mail: hlzhao@ustb.edu.cn [School of Materials Science and Engineering, University of Science and Technology Beijing, 30 Xueyuan Road, Haidian District, Beijing 100083 (China); Beijing Key Lab of New Energy Materials and Technologies, Beijing 100083 (China); Zeng, Zhipeng; Gao, Chunhui; Liu, Xin; Zhang, Tianhou [School of Materials Science and Engineering, University of Science and Technology Beijing, 30 Xueyuan Road, Haidian District, Beijing 100083 (China)

    2015-02-28

    Highlights: • 3D hierarchical NiO porous nano/microspheres were prepared via a hydrothermal route. • Loose NiO microsphere is composed of a large number of cross-linked nanoparticles. • A possible self-assembly mechanism is illustrated in detail. • High specific capacity, good cycleability and superior rate-capability are achieved. - Abstract: Self-assembled three-dimensional hierarchical NiO nano/microspheres were fabricated via a hydrothermal route. The obtained NiO presents a micro-sized porous spherical morphology which is composed of a large number of primary NiO nanoparticles linked together with an ordered fashion. As anode material for lithium ion batteries, NiO nano/microspheres exhibit stable reversible capacity of over 700 mAh g{sup −1} and good rate capability. The superior electrochemical performance could be attributed to the merits of the unique three-dimensional hierarchical porous nano/microstructure.

  2. Graphitic Carbon-Coated FeSe2 Hollow Nanosphere-Decorated Reduced Graphene Oxide Hybrid Nanofibers as an Efficient Anode Material for Sodium Ion Batteries

    Science.gov (United States)

    Cho, Jung Sang; Lee, Jung-Kul; Kang, Yun Chan

    2016-01-01

    A novel one-dimensional nanohybrid comprised of conductive graphitic carbon (GC)-coated hollow FeSe2 nanospheres decorating reduced graphene oxide (rGO) nanofiber (hollow nanosphere FeSe2@GC–rGO) was designed as an efficient anode material for sodium ion batteries and synthesized by introducing the nanoscale Kirkendall effect into the electrospinning method. The electrospun nanofibers transformed into hollow nanosphere FeSe2@GC–rGO hybrid nanofibers through a Fe@GC–rGO intermediate. The discharge capacities of the bare FeSe2 nanofibers, nanorod FeSe2–rGO–amorphous carbon (AC) hybrid nanofibers, and hollow nanosphere FeSe2@GC–rGO hyrbid nanofibers at a current density of 1 A g−1 for the 150th cycle were 63, 302, and 412 mA h g−1, respectively, and their corresponding capacity retentions measured from the 2nd cycle were 11, 73, and 82%, respectively. The hollow nanosphere FeSe2@GC–rGO hybrid nanofibers delivered a high discharge capacity of 352 mA h g−1 even at an extremely high current density of 10 A g−1. The enhanced electrochemical properties of the hollow nanosphere FeSe2@GC–rGO composite nanofibers arose from the synergetic effects of the FeSe2 hollow morphology and highly conductive rGO matrix. PMID:27033096

  3. One-pot solvothermal synthesis of graphene wrapped rice-like ferrous carbonate nanoparticles as anode materials for high energy lithium-ion batteries

    Science.gov (United States)

    Zhang, Fan; Zhang, Ruihan; Feng, Jinkui; Ci, Lijie; Xiong, Shenglin; Yang, Jian; Qian, Yitai; Li, Lifei

    2014-11-01

    Well dispersed rice-like FeCO3 nanoparticles were produced and combined with reduced graphene oxide (RGO) via a one-pot solvothermal route. SEM characterization shows that rice-like FeCO3 nanoparticles are homogeneously anchored on the surface of the graphene nanosheets; the addition of RGO is helpful to form a uniform morphology and reduce the particle size of FeCO3 to nano-grade. As anode materials for lithium-ion batteries, the FeCO3/RGO nanocomposites exhibit significantly improved lithium storage properties with a large reversible capacity of 1345 mA h g-1 for the first cycle and a capacity retention of 1224 mA h g-1 after 50 cycles with a good rate capability compared with pure FeCO3 particles. The superior electrochemical performance of the FeCO3/RGO nanocomposite electrode compared to the pure FeCO3 electrode can be attributed to the well dispersed RGO which enhances the electronic conductivity and accommodates the volume change during the conversion reactions. Our study shows that the FeCO3/RGO nanocomposite could be a suitable candidate for high capacity lithium-ion batteries.

  4. 锂离子电池硅基负极材料研究进展%Research on the Silicon-Based Anode Material for Lithium Ion Battery

    Institute of Scientific and Technical Information of China (English)

    张利

    2012-01-01

    硅是青海省储量丰富的资源之一,因其储锂容量高、安全性能优越,而成为锂离子电池理想的负极材料,但由于硅在深度嵌脱锂时体积效应大,易与导电介质、集流体失去电接触,造成电极循环性能迅速下降.对抑制其体积效应、增加其电导率的“低维化”和“复合化”两种技术进行了介绍.%Silicon is one of the main resources in Qinghai province. Due to the lower reactivity against e-lectrolyte than lithium and the lower insertion/extraction potential for lithium ion, silicon is an ideal anode material for lithium-ion rechargeable batteries. However,the application of silicon has been hindered by severe volume change upon Ii * insertion and extraction which will cause poor cycling stability. To o-vercome the problems, two main approaches which can realize the alleviation of the severe volume change and the reduction of the charge transfer resistance of silicon have been reviewed.

  5. Controlled Synthesis of Carbon Nanofibers Anchored with Zn(x)Co(3-x)O4 Nanocubes as Binder-Free Anode Materials for Lithium-Ion Batteries.

    Science.gov (United States)

    Chen, Renzhong; Hu, Yi; Shen, Zhen; Chen, Yanli; He, Xia; Zhang, Xiangwu; Zhang, Yan

    2016-02-01

    The direct growth of complex ternary metal oxides on three-dimensional conductive substrates is highly desirable for improving the electrochemical performance of lithium-ion batteries (LIBs). We herein report a facile and scalable strategy for the preparation of carbon nanofibers (CNFs) anchored with ZnxCo3-xO4 (ZCO) nanocubes, involving a hydrothermal process and thermal treatment. Moreover, the size of the ZCO nanocubes was adjusted by the quantity of urea used in the hydrothermal process. Serving as a binder-free anode material for LIBs, the ZnCo2O4/CNFs composite prepared using 1.0 mmol of urea (ZCO/CNFs-10) exhibited excellent electrochemical performance with high reversible capacity, excellent cycling stability, and good rate capability. More specifically, a high reversible capacity of ∼600 mAh g(-1) was obtained at a current density of 0.5 C following 300 charge-discharge cycles. The excellent electrochemical performance could be associated with the controllable size of the ZCO nanocubes and synergistic effects between ZCO and the CNFs. PMID:26761129

  6. Facile preparation of 3D hierarchical porous carbon from lignin for the anode material in lithium ion battery with high rate performance

    International Nuclear Information System (INIS)

    Graphical abstract: Hierarchical porous carbon with 3D macroporous structure is prepared via a facile method and displays high lithium ion storage capacity and rate capability. - Highlights: • Hierarchical porous carbon is prepared from lignin via a facile method. • KOH acts both as activating agent and template in the preparation process. • Lignin based hierarchical porous carbon displays high lithium storage capacity. • Lignin based hierarchical porous carbon displays stable cycling stability. - Abstract: Hierarchical porous carbon derived from lignin (denoted as LHPC) was prepared via a facile method. In this method, KOH acts both as activating agent and template. The obtained LHPC was composed of unique 3D macroporous network with mesopores and micropores decorated on carbon walls. LHPC was further applied as the anode material of lithium ion battery and displayed a stable, high capacity of 470 mAh g−1 after 400 galvanostatic charge-discharge cycles at a current density of 200 mA g−1. Furthermore, LHPC displayed high cycling stability and perfect rate capability. This facile method for the preparation of LHPC offers a new route for the preparation of a series of hierarchical porous carbons for the application in supercapacitors, fuel cells, lithium ion batteries, etc

  7. Template-free electrodeposition of AlFe alloy nanowires from a room-temperature ionic liquid as an anode material for Li-ion batteries.

    Science.gov (United States)

    Chen, Gang; Chen, Yuqi; Guo, Qingjun; Wang, Heng; Li, Bing

    2016-08-15

    AlFe alloy nanowires were directly electrodeposited on copper substrates from trimethylamine hydrochloride (TMHC)-AlCl3 ionic liquids with small amounts of FeCl3 at room temperature without templates. Coin cells composed of AlFe alloy nanowire electrodes and lithium foils were assembled to characterize the alloy electrochemical properties by galvanostatic charge/discharge tests. Effects of FeCl3 concentration, potential and temperature on the alloy morphology, composition and cyclic performance were examined. Addition of Fe into the alloy changed the nanowires from a 'hill-like' bulk morphology to a free-standing morphology, and increased the coverage area of the alloy on Cu substrates. As an inactive element, Fe could also buffer the alloys' large volume changes during Li intercalation and deintercalation. AlFe alloy nanowires composed of a small amount of Fe with an average diameter of 140 nm exhibited an outstanding cyclic performance and delivered a specific capacity of about 570 mA h g(-1) after 50 cycles. This advanced template-free method for the direct preparation of high performance nanostructure AlFe alloy anode materials is quite simple and inexpensive, which presents a promising prospect for practical application in Li-ion batteries. PMID:27200436

  8. Investigation of a porous NiSi2/Si composite anode material used for lithium-ion batteries by X-ray absorption spectroscopy

    Science.gov (United States)

    Zhou, Dong; Jia, Haiping; Rana, Jatinkumar; Placke, Tobias; Klöpsch, Richard; Schumacher, Gerhard; Winter, Martin; Banhart, John

    2016-08-01

    Local structural changes in a porous NiSi2/Si composite anode material are investigated by X-ray absorption spectroscopy. It is observed that the NiSi2 phase shows a strong metal-metal bond character and no clear changes can be observed in XANES during lithiation and de-lithiation. The variation of the number of nearest neighbors of the Ni atom for the 1st coordinate Ni-Si shell and σ2 in the 1st cycle, both determined by refinement, demonstrates that NiSi2 can partially react with lithium during discharge and charge. A partially reversible non-stoichiometric compound NiSi2-y is formed during cell operation, the crystal structure of which is the same as that of the NiSi2 phase. It can be concluded that NiSi2 in the composite not only accommodates the pronounced volume changes caused by the lithium uptake into silicon, but also contributes to the reversible capacity of the cell.

  9. Ultrasonication-assisted ultrafast preparation of multiwalled carbon nanotubes/Au/Co3O4 tubular hybrids as superior anode materials for oxygen evolution reaction

    Science.gov (United States)

    Fang, Yiyun; Li, Xinzhe; Hu, Yiping; Li, Feng; Lin, Xiaoqing; Tian, Min; An, Xingcai; Fu, Yan; Jin, Jun; Ma, Jiantai

    2015-12-01

    Efficient and simple operation electrocatalysts for the oxygen evolution reaction (OER) are essential components of renewable energy technologies. Here, a novel, simple, and efficient routine is presented for the first time by constructing a high-efficiency anode catalyst for OER. With the aid of high intensity ultrasound, a uniformly loading, conductive multiwalled carbon nanotubes/metal/transition metal-oxide (CNTs-Au@Co3O4) tubular hybrids is synthesized. In alkaline media, the materials catalyze OER with an onset potential of 1.56 V vs. reversible hydrogen electrode (RHE) and overpotential only of 350 mV to achieve a stable current density of 10 mA cm-2 for at least 25 h. The unusual catalytic activity and stability is due to the following elements. Firstly, the tubular architecture not only provides sufficient active centers for OER, but also improves rapid mass/charge transport. Secondly, Co3O4 layer protects Au nanoparticles (NPs) against detachment. In addition, we also prove that the highest electronegativity metal Au accelerate the formation of catalytic active sites of CoIV species for OER. It is believed that this simple preparation method paves a way to fabricate a range of CNTs/metal/metal-oxide based composites as superior OER catalysts.

  10. Hydrogenated TiO2 Branches Coated Mn3O4 Nanorods as an Advanced Anode Material for Lithium Ion Batteries.

    Science.gov (United States)

    Wang, Nana; Yue, Jie; Chen, Liang; Qian, Yitai; Yang, Jian

    2015-05-20

    Rational design and delicate control on the component, structure, and surface of electrodes in lithium ion batteries are highly important to their performances in practical applications. Compared with various components and structures for electrodes, the choices for their surface are quite limited. The most widespread surface for numerous electrodes, a carbon shell, has its own issues, which stimulates the desire to find another alternative surface. Here, hydrogenated TiO2 is exemplified as an appealing surface for advanced anodes by the growth of ultrathin hydrogenated TiO2 branches on Mn3O4 nanorods. High theoretical capacity of Mn3O4 is well matched with low volume variation (∼4%), enhanced electrical conductivity, good cycling stability, and rate capability of hydrogenated TiO2, as demonstrated in their electrochemical performances. The proof-of-concept reveals the promising potential of hydrogenated TiO2 as a next-generation material for the surface in high-performance hybrid electrodes. PMID:25928277

  11. Porous γ-Fe2O3 spheres coated with N-doped carbon from polydopamine as Li-ion battery anode materials

    Science.gov (United States)

    Liang, Jin; Xiao, Chunhui; Chen, Xu; Gao, Ruixia; Ding, Shujiang

    2016-05-01

    Nitrogen doping has been demonstrated to play a crucial role in controlling the electronic properties of carbon-based composites. In this paper, nitrogen-doped carbon coated γ-Fe2O3 (NC@γ-Fe2O3) composite was successfully fabricated through a facile and high-yield strategy, including a hydrothermal reaction process for porous γ-Fe2O3 and a subsequent coating of nitrogen-doped carbon by using dopamine as precursor. The resulting composite combines the superior properties of porous Fe2O3 and heteroatom-doped conductive carbon layer derived from polydopamine. When used as the anode material of the lithium-ion battery, the as-prepared NC@γ-Fe2O3 composite exhibits excellent lithium storage properties in terms of high capacity, stable cycling performance (869.6 mAh g‑1 at the current density of 0.5 A g‑1 after 150 cycles) and excellent rate capability.

  12. Preparation and Electrochemical Performance of Nano-Co3O4 Anode Materials from Spent Li-Ion Batteries for Lithium-Ion Batteries

    Institute of Scientific and Technical Information of China (English)

    Chuanyue Hu; Jun Guo; Jin Wen; Yangxi Peng

    2013-01-01

    A hydrometallurgical process for the recovery of cobalt oxalate from spent lithium-ion batteries was used to recycle cobalt compound by using alkali leaching,reductive acid leaching and chemical deposition of cobalt oxalate.The recycled cobalt oxalate was used to synthesize nano-Co3O4 anode material by sol-gel method.The samples were characterized by thermal gravity analysis and differential thermal analysis (TGA/DTA),X-ray diffraction (XRD),scanning electron microscopy (SEM) and charge/discharge measurements.The influence of molar ratio of Co2+ to citric acid and calcination temperature on the structure and electrochemical performance of nano-Co3O4 was evaluated.As the molar ratio of Co2+ to citric acid is 1:1,the face-centered cubic (fcc) Co3O4 powder shows the discharge capacity of 760.9 mA h g-1,the high coulombic efficiency of 99.7% in the first cycle at the current density of 125 mA g-1,and the excellent cycling performance with the reversible capacity of 442.3 mA h g-1 after 20 cycles at the current density of 250 mA g-1.

  13. Graphitic Carbon-Coated FeSe2 Hollow Nanosphere-Decorated Reduced Graphene Oxide Hybrid Nanofibers as an Efficient Anode Material for Sodium Ion Batteries

    Science.gov (United States)

    Cho, Jung Sang; Lee, Jung-Kul; Kang, Yun Chan

    2016-04-01

    A novel one-dimensional nanohybrid comprised of conductive graphitic carbon (GC)-coated hollow FeSe2 nanospheres decorating reduced graphene oxide (rGO) nanofiber (hollow nanosphere FeSe2@GC-rGO) was designed as an efficient anode material for sodium ion batteries and synthesized by introducing the nanoscale Kirkendall effect into the electrospinning method. The electrospun nanofibers transformed into hollow nanosphere FeSe2@GC-rGO hybrid nanofibers through a Fe@GC-rGO intermediate. The discharge capacities of the bare FeSe2 nanofibers, nanorod FeSe2-rGO-amorphous carbon (AC) hybrid nanofibers, and hollow nanosphere FeSe2@GC-rGO hyrbid nanofibers at a current density of 1 A g-1 for the 150th cycle were 63, 302, and 412 mA h g-1, respectively, and their corresponding capacity retentions measured from the 2nd cycle were 11, 73, and 82%, respectively. The hollow nanosphere FeSe2@GC-rGO hybrid nanofibers delivered a high discharge capacity of 352 mA h g-1 even at an extremely high current density of 10 A g-1. The enhanced electrochemical properties of the hollow nanosphere FeSe2@GC-rGO composite nanofibers arose from the synergetic effects of the FeSe2 hollow morphology and highly conductive rGO matrix.

  14. A novel radial anode layer ion source for inner wall pipe coating and materials modification--hydrogenated diamond-like carbon coatings from butane gas.

    Science.gov (United States)

    Murmu, Peter P; Markwitz, Andreas; Suschke, Konrad; Futter, John

    2014-08-01

    We report a new ion source development for inner wall pipe coating and materials modification. The ion source deposits coatings simultaneously in a 360° radial geometry and can be used to coat inner walls of pipelines by simply moving the ion source in the pipe. Rotating parts are not required, making the source ideal for rough environments and minimizing maintenance and replacements of parts. First results are reported for diamond-like carbon (DLC) coatings on Si and stainless steel substrates deposited using a novel 360° ion source design. The ion source operates with permanent magnets and uses a single power supply for the anode voltage and ion acceleration up to 10 kV. Butane (C4H10) gas is used to coat the inner wall of pipes with smooth and homogeneous DLC coatings with thicknesses up to 5 μm in a short time using a deposition rate of 70 ± 10 nm min(-1). Rutherford backscattering spectrometry results showed that DLC coatings contain hydrogen up to 30 ± 3% indicating deposition of hydrogenated DLC (a-C:H) coatings. Coatings with good adhesion are achieved when using a multiple energy implantation regime. Raman spectroscopy results suggest slightly larger disordered DLC layers when using low ion energy, indicating higher sp(3) bonds in DLC coatings. The results show that commercially interesting coatings can be achieved in short time. PMID:25173323

  15. High performance amorphous-Si@SiOx/C composite anode materials for Li-ion batteries derived from ball-milling and in situ carbonization

    Science.gov (United States)

    Wang, Dingsheng; Gao, Mingxia; Pan, Hongge; Wang, Junhua; Liu, Yongfeng

    2014-06-01

    Amorphous-Si@SiOx/C composites with amorphous Si particles as core and coated with a double layer of SiOx and carbon are prepared by ball-milling crystal micron-sized silicon powders and carbonization of the citric acid intruded in the ball-milled Si. Different ratios of Si to citric acid are used in order to optimize the electrochemical performance. It is found that SiOx exists naturally at the surfaces of raw Si particles and its content increases to ca. 24 wt.% after ball-milling. With an optimized Si to citric acid weight ratio of 1/2.5, corresponding to 8.4 wt.% C in the composite, a thin carbon layer is coated on the surfaces of a-Si@SiOx particles, moreover, floc-like carbon also forms and connects the carbon coated a-Si@SiOx particles. The composite provides a capacity of 1450 mA h g-1 after 100 cycles at a current density of 100 mA g1, and a capacity of 1230 mA h g-1 after 100 cycles at 500 mA g1 as anode material for lithium-ion batteries. Effects of ball-milling and the addition of citric acid on the microstructure and electrochemical properties of the composites are revealed and the mechanism of the improvement in electrochemical properties is discussed.

  16. Mesoporous MFe2O4 (M = Mn, Co, and Ni) for anode materials of lithium-ion batteries: Synthesis and electrochemical properties

    International Nuclear Information System (INIS)

    Highlights: • MFe2O4 (M = Mn, Co, and Ni) are synthesized by a template-free hydrothermal method. • The mesoporous morphology is formed by self-assembly of crystal nucleus. • The mesporous MnFe2O4 have the active phase and the synergy for Li-ion storage. - Abstract: The MFe2O4 (M = Mn, Co, and Ni) mesoporous spheres with an average diameter of 250 nm were synthesized through a template-free hydrothermal method. The mesoporous MnFe2O4 with a large surface area of 87.5 m2/g and an average pore size of 27.52 nm were obtained. As the anode materials for Li-ion batteries, the mesoporous MnFe2O4 exhibits excellent initial charge and discharge capacities of 1010 and 642.5 mA h/g. After 50 cycles, the discharge capacity could still remain at 379 mA h/g. The results showed that the active phase and the synergy between different metal oxides greatly improved the electrochemical performance, and the mesoporous composite could stabilize the structure of the electrodes

  17. Facile synthesis of porous NiCo2O4 microflowers as high-performance anode materials for advanced lithium-ion batteries

    International Nuclear Information System (INIS)

    Graphical abstract: - Abstract: Porous NiCo2O4 microflowers having very high Brunner-Emmett-Teller (BET) surface area (∼109.283 m2/g) are fabricated by a facile solvothermal method followed by calcinating the Co-Ni hydroxides precursor in air. The as-prepared porous NiCo2O4 microflowers exhibit excellent cycling stability (952 mA h g−1 at a current density of 100 mA g−1 after 60 cycles and 720 mA h g−1 at a current density of 500 mA g−1 after 100 cycles). This outstanding electrochemical performance is attributed to the unique hierarchical structure and high porosity, which can provide enough space to buffer the volume expansion during the discharge and charge processes, increase the contact area between the electrode and electrolyte, and reduce the transport lengths of both lithium ions and electrons. The porous NiCo2O4 microflowers show great potential in high-capacity anode materials for next-generation lithium-ion batteries

  18. Co3V2O8 Sponge Network Morphology Derived from Metal-Organic Framework as an Excellent Lithium Storage Anode Material.

    Science.gov (United States)

    Soundharrajan, Vaiyapuri; Sambandam, Balaji; Song, Jinju; Kim, Sungjin; Jo, Jeonggeun; Kim, Seokhun; Lee, Seulgi; Mathew, Vinod; Kim, Jaekook

    2016-04-01

    Metal-organic framework (MOF)-based synthesis of battery electrodes has presntly become a topic of significant research interest. Considering the complications to prepare Co3V2O8 due to the criticality of its stoichiometric composition, we report on a simple MOF-based solvothermal synthesis of Co3V2O8 for use as potential anodes for lithium battery applications. Characterizations by X-ray diffraction, X-ray photoelectron spectroscopy, high resolution electron microscopy, and porous studies revealed that the phase pure Co3V2O8 nanoparticles are interconnected to form a sponge-like morphology with porous properties. Electrochemical measurements exposed the excellent lithium storage (∼1000 mAh g(-1) at 200 mA g(-1)) and retention properties (501 mAh g(-1) at 1000 mA g(-1) after 700 cycles) of the prepared Co3V2O8 electrode. A notable rate performance of 430 mAh g(-1) at 3200 mA g(-1) was also observed, and ex situ investigations confirmed the morphological and structural stability of this material. These results validate that the unique nanostructured morphology arising from the use of the ordered array of MOF networks is favorable for improving the cyclability and rate capability in battery electrodes. The synthetic strategy presented herein may provide solutions to develop phase pure mixed metal oxides for high-performance electrodes for useful energy storage applications.

  19. Preparation of a Binder-Free Three-Dimensional Carbon Foam/Silicon Composite as Potential Material for Lithium Ion Battery Anodes.

    Science.gov (United States)

    Roy, Amit K; Zhong, Mingjie; Schwab, Matthias Georg; Binder, Axel; Venkataraman, Shyam S; Tomović, Željko

    2016-03-23

    We report a novel three-dimensional nitrogen containing carbon foam/silicon (CFS) composite as potential material for lithium ion battery anodes. Carbon foams were prepared by direct carbonization of low cost, commercially available melamine formaldehyde (MF, Basotect) foam precursors. The carbon foams thus obtained display a three-dimensional interconnected macroporous network structure with good electrical conductivity (0.07 S/cm). Binder free CFS composites used for electrodes were prepared by immersing the as-fabricated carbon foam into silicon nanoparticles dispersed in ethanol followed by solvent evaporation and secondary pyrolysis. In order to substantiate this new approach, preliminary electrochemical testing has been done. The first results on CFS electrodes demonstrated initial capacity of 1668 mAh/g with 75% capacity retention after 30 cycles of subsequent charging and discharging. In order to further enhance the electrochemical performance, silicon nanoparticles were additionally coated with a nitrogen containing carbon layer derived from codeposited poly(acrylonitrile). These carbon coated CFS electrodes demonstrated even higher performance with an initial capacity of 2100 mAh/g with 92% capacity retention after 30 cycles of subsequent charging and discharging. PMID:26909748

  20. Electrochemical performance of potassium-doped wüstite nanoparticles supported on graphene as an anode material for lithium ion batteries

    Science.gov (United States)

    Jung, Dong-Won; Jeong, Jae-Hoon; Han, Sang-Wook; Oh, Eun-Suok

    2016-05-01

    A graphene composite with potassium-doped FeO nanoparticles (K-FeO/graphene) is synthesized by the thermal diffusion of potassium into Fe2O3/graphene using polyol reduction. This is applied as anode material in lithium ion batteries in order to enhance the electrochemical performance of conventional iron oxides (hematite or magnetite). Rhombohedral Fe2O3 crystals are transformed into face-centered cubic FeO crystals, which show a broad d-spacing (5.2 Å) between their (111) crystal planes, by the calcination of potassium-added Fe2O3/graphene. Because of its structural characteristics, the K-FeO/graphene composite demonstrates an excellent discharge capacity of 1776 mA h g-1 at the 50th cycle at a current of 100 mA h g-1 with stable capacity retention. Even with the very high current density of 18.56 A g-1, its capacity remains at 851 mA h g-1 after 800 cycles.

  1. Synthesis of TiO{sub 2} by electrochemical method from TiCl{sub 4} solution as anode material for lithium-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Nur, Adrian, E-mail: adriannur@staff.uns.ac.id; Purwanto, Agus; Jumari, Arif; Dyartanti, Endah R.; Sari, Sifa Dian Permata; Hanifah, Ita Nur [Research Group of Advanced Material, Department of Chemical Engineering, Sebelas Maret University, Jl. Ir. Sutami 36 A Kentingan, Surakarta Indonesia 57126 (Indonesia)

    2016-02-08

    Metal oxide combined with graphite becomes interesting composition. TiO{sub 2} is a good candidate for Li ion battery anode because of cost, availability of sufficient materials, and environmentally friendly. TiO{sub 2} gravimetric capacity varied within a fairly wide range. TiO{sub 2} crystals form highly depends on the synthesis method used. The electrochemical method is beginning to emerge as a valuable option for preparing TiO{sub 2} powders. Using the electrochemical method, the particle can easily be controlled by simply adjusting the imposed current or potential to the system. In this work, the effects of some key parameters of the electrosynthesis on the formation of TiO{sub 2} have been investigated. The combination of graphite and TiO{sub 2} particle has also been studied for lithium-ion batteries. The homogeneous solution for the electrosynthesis of TiO{sub 2} powders was TiCl{sub 4} in ethanol solution. The electrolysis was carried out in an electrochemical cell consisting of two carbon electrodes with dimensions of (5 × 2) cm. The electrodes were set parallel with a distance of 2.6 cm between the electrodes and immersed in the electrolytic solution at a depth of 2 cm. The electrodes were connected to the positive and negative terminals of a DC power supply. The electrosynthesis was performed galvanostatically at 0.5 to 2.5 hours and voltages were varied from 8 to 12 V under constant stirring at room temperature. The resulted suspension was aged at 48 hrs, filtered, dried directly in an oven at 150°C for 2 hrs, washed 2 times, and dried again 60 °C for 6 hrs. The particle product has been used to lithium-ion battery as anode. Synthesis of TiO{sub 2} particle by electrochemical method at 10 V for 1 to 2.5 hrs resulted anatase and rutile phase.

  2. Research status and development trend on Si-based anode materials of lithium ion batteries%锂离子电池硅基负极材料研究现状与发展趋势

    Institute of Scientific and Technical Information of China (English)

    张培新; 汪静伟; 黄亮; 张冬云

    2014-01-01

    硅基负极材料因具有高电化学容量是一种极具发展前景的锂离子电池负极材料。评述单质硅、硅-金属合金、硅-碳复合材料以及其他硅基复合材料作为锂离子二次电池负极材料的最新研究成果,分析锂离子电池硅负极材料存在问题,探讨硅基负极材料的合成、制备工艺以及未来硅基材料的研究方向和应用前景。分析结果表明,通过硅的纳米化、无定形化、合金化及复合化等技术手段,实现硅基负极材料同时兼备高容量、长寿命、高库伦效率和倍率性能,是未来的主要发展方向。%The silicon-based anode materials are of great importance for lithium ion batteries ( LIBs) because of their high capacity. This paper reviews the latest research achievements of the silicon, silicon-metal alloys, silicon-carbon composites and other composite materials as anodes materials and discusses their research and application prospects. It also analyzes the existing problems of pure silicon anodes and focuses mainly on the novel silicon based anode materials. Regarding future research and application, the predominant direction will be to promote both cycle performance and electrochemical performance through the comprehensive application of nanocrystallization, amor-phization, alloying and compounding of silicon-based materials.

  3. One-pot hydrothermal synthesis of Nitrogen-doped graphene as high-performance anode materials for lithium ion batteries

    Science.gov (United States)

    Xing, Zheng; Ju, Zhicheng; Zhao, Yulong; Wan, Jialu; Zhu, Yabo; Qiang, Yinghuai; Qian, Yitai

    2016-05-01

    Nitrogen-doped (N-doped) graphene has been prepared by a simple one-step hydrothermal approach using hexamethylenetetramine (HMTA) as single carbon and nitrogen source. In this hydrothermal process, HMTA pyrolyzes at high temperature and the N-doped graphene subsequently self-assembles on the surface of MgO particles (formed by the Mg powder reacting with H2O) during which graphene synthesis and nitrogen doping are simultaneously achieved. The as-synthesized graphene with incorporation of nitrogen groups possesses unique structure including thin layer thickness, high surface area, mesopores and vacancies. These structural features and their synergistic effects could not only improve ions and electrons transportation with nanometer-scale diffusion distances but also promote the penetration of electrolyte. The N-doped graphene exhibits high reversible capacity, superior rate capability as well as long-term cycling stability, which demonstrate that the N-doped graphene with great potential to be an efficient electrode material. The experimental results provide a new hydrothermal route to synthesize N-doped graphene with potential application for advanced energy storage, as well as useful information to design new graphene materials.

  4. Influence of the operating parameters over the current efficiency and corrosion rate in the Hall-Heroult aluminum cell with tin oxide anode substrate material

    Institute of Scientific and Technical Information of China (English)

    Virgil Constantin

    2015-01-01

    A systematic laboratory study was conducted on current efficiency and corrosion obtalned in cryolite–alumina melts with SnO2–Sb2O3–CuO ceramic inert anodes. The current efficiency (CE) was determined by measuring the total amount of oxygen evolved at the anode and was found to be~95%. The influence of operating parameters (inter-elec-trode distance, temperature and current density) was evaluated. The quantitative interdependencies as wel as the ranges of CE optimal values were established (2–3 cm, 940–960 °C and 0.7–0.8 A·cm−2). The corrosion process of these anodes was evaluated by the mass loss method. The evaluation also took care of the corrosion data, as the prob-lem of the anode corrosion appeared to be the maln obstacle for the use of those anodes in the commercial cel s. Low-ering of the ACD up to 2 cm did not aggravate anode corrosion.

  5. Nitrogen-doped carbon/graphene hybrid anode material for sodium-ion batteries with excellent rate capability

    Science.gov (United States)

    Liu, Huan; Jia, Mengqiu; Cao, Bin; Chen, Renjie; Lv, Xinying; Tang, Renjie; Wu, Feng; Xu, Bin

    2016-07-01

    Nitrogen-doped carbon/graphene (NCG) hybrid materials were prepared by an in-situ polymerization and followed pyrolysis for sodium-ion batteries. The NCG has a large interlayer distance (0.360 nm) and a high nitrogen content of 7.54 at%, resulting in a high reversible sodium storage capacity of 336 mAh g-1 at 30 mA g-1. The NCG shows a sandwich-like structure, i.e. nitrogen-doped carbon nanosheets closely coated on both sides of graphene. The carbon nanosheets shorten the ion diffusion distance, while the sandwiched graphene with high electronic conductivity guarantees fast electron transport, making the NCG exhibit excellent rate capability (94 mAh g-1 at 5 A g-1). It also exhibits good cycle stability with a capacity retention of 89% after 200 cycles at 50 mA g-1.

  6. Solvothermal preparation of ZnO nanorods as anode material for improved cycle life Zn/AgO batteries.

    Directory of Open Access Journals (Sweden)

    Shafiq Ullah

    Full Text Available Nano materials with high surface area increase the kinetics and extent of the redox reactions, thus resulting in high power and energy densities. In this study high surface area zinc oxide nanorods have been synthesized by surfactant free ethylene glycol assisted solvothermal method. The nanorods thus prepared have diameters in the submicron range (300 ~ 500 nm with high aspect ratio. They have uniform geometry and well aligned direction. These nanorods are characterized by XRD, SEM, Specific Surface Area Analysis, solubility in alkaline medium, EDX analysis and galvanostatic charge/discharge studies in Zn/AgO batteries. The prepared zinc oxide nanorods have low solubility in alkaline medium with higher structural stability, which imparts the improved cycle life stability to Zn/AgO cells.

  7. Microspheric Na2Ti3O7 consisting of tiny nanotubes: an anode material for sodium-ion batteries with ultrafast charge-discharge rates

    Science.gov (United States)

    Wang, Wei; Yu, Chengjun; Lin, Zheshuai; Hou, Jungang; Zhu, Hongmin; Jiao, Shuqiang

    2012-12-01

    Conventionally, rechargeable batteries with a fast charge-discharge rate, while being able to be implemented in large-scale applications with low prices, are critical for new energy storage systems. In this work, first-principles simulations were employed to theoretically investigate the insertion of sodium into the Na2Ti3O7 structure. The result discovered that the theoretical capacity of Na2Ti3O7 was 311 mA h g-1. Furthermore, a microspheric Na2Ti3O7 material consisting of tiny nanotubes of ca. 8 nm in outside diameter and a few hundred nanometers in length has been synthesized. The galvanostatic charge-discharge measurements, using the as-prepared Na2Ti3O7 nanotubes as a working electrode with a voltage range of 0.01-2.5 V vs. Na+/Na, disclosed that a high capacity was maintained even under an ultrafast charge-discharge rate. At a current density of 354 mA g-1, the discharge capacity was maintained at 108 mA h g-1 over 100 cycles. Even at a very large current density of 3540 mA g-1, the discharge capacity was still 85 mA h g-1. HRTEM analysis and electrochemical tests proved that sodium ions could not only intercalate into the Na2Ti3O7 crystal, but could also be stored in the intracavity of the nanotubes. All of the results disclose that the as-prepared Na2Ti3O7 nanotubes are able to be used as anode materials in large-scale applications for rechargeable sodium-ion batteries at low cost while maintaining excellent performance.

  8. An Insoluble Titanium-Lead Anode for Sulfate Electrolytes

    Energy Technology Data Exchange (ETDEWEB)

    Ferdman, Alla

    2005-05-11

    The project is devoted to the development of novel insoluble anodes for copper electrowinning and electrolytic manganese dioxide (EMD) production. The anodes are made of titanium-lead composite material produced by techniques of powder metallurgy, compaction of titanium powder, sintering and subsequent lead infiltration. The titanium-lead anode combines beneficial electrochemical behavior of a lead anode with high mechanical properties and corrosion resistance of a titanium anode. In the titanium-lead anode, the titanium stabilizes the lead, preventing it from spalling, and the lead sheathes the titanium, protecting it from passivation. Interconnections between manufacturing process, structure, composition and properties of the titanium-lead composite material were investigated. The material containing 20-30 vol.% of lead had optimal combination of mechanical and electrochemical properties. Optimal process parameters to manufacture the anodes were identified. Prototypes having optimized composition and structure were produced for testing in operating conditions of copper electrowinning and EMD production. Bench-scale, mini-pilot scale and pilot scale tests were performed. The test anodes were of both a plate design and a flow-through cylindrical design. The cylindrical anodes were composed of cylinders containing titanium inner rods and fitting over titanium-lead bushings. The cylindrical design allows the electrolyte to flow through the anode, which enhances diffusion of the electrolyte reactants. The cylindrical anodes demonstrate higher mass transport capabilities and increased electrical efficiency compared to the plate anodes. Copper electrowinning represents the primary target market for the titanium-lead anode. A full-size cylindrical anode performance in copper electrowinning conditions was monitored over a year. The test anode to cathode voltage was stable in the 1.8 to 2.0 volt range. Copper cathode morphology was very smooth and uniform. There was no

  9. Research Advances in Silicon-Based Anode Materials of High Capacity Lithium Ion Battery%高容量型锂离子电池硅基负极材料的研究

    Institute of Scientific and Technical Information of China (English)

    胡社军; 张苗; 侯贤华; 王洁; 李敏; 刘祥

    2013-01-01

    Due to its high capacity , silicon based anode materials have been widely studied in recent years .How-ever,the commercialization of silicon-based materials as the anode of lithium-ion batteries( LIBs) has been hindered by the huge volume change , poor cycle life and low initial coulombic efficiency during the charge /discharge process .This article analyses the insertion/interinsertion lithium ion principle of silicon anodes , reviews the change of the crystal structure and the surface/interface of Si-based material during the intercalation/deintercalation of lith-ium, and the methods for improving the electrochemical performance .The prospects of silicon-based materials as the anode of LIBs are also discussed .%硅基负极材料由于具有高容量而被广泛研究,该材料在充/放电过程中巨大的体积变化、低的循环寿命和初始库仑效率阻碍了其商业化应用。在作者多年从事硅基负极材料的研究基础上,分析了硅基负极材料的工作原理,回顾了Si负极在脱/嵌锂过程中的晶体结构、表面/界面的变化以及提高其电化学性能的方法,讨论了锂离子电池硅基负极材料的前景。

  10. 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

  11. Synthesis of NiCo2O4 Microellipsoids as Anode Material for Lithium-Ion Batteries

    Science.gov (United States)

    Zheng, Hao; Xu, Shan; Li, Lin; Feng, Chuanqi; Wang, Shiquan

    2016-10-01

    NiCo2O4 microellipsoids have been synthesized by a rheological-phase hydrothermal method to obtain the precursors followed by annealing at 450°C for 4 h. The effects of different hydrothermal temperatures (140°C to 180°C) on the morphologies and electrochemical properties of the final product were systematically investigated. NiCo2O4 microellipsoids synthesized at 180°C exhibited the best electrochemical properties, with high reversible capacity (921 mAh g-1 at current density of 100 mA g-1) and good cycling stability (820 mAh g-1 even after 100 cycles), compared with other samples. They also delivered discharge capacity of 586 mAh g-1 at relatively high current density of 800 mA g-1. The remarkable electrochemical performance of the NiCo2O4 microellipsoids can be attributed to their high surface area. These results indicate that NiCo2O4 microellipsoids could be a promising electrode material for lithium-ion batteries.

  12. Borophene as an anode material for Ca, Mg, Na or Li ion storage: A first-principle study

    Science.gov (United States)

    Mortazavi, Bohayra; Dianat, Arezoo; Rahaman, Obaidur; Cuniberti, Gianaurelio; Rabczuk, Timon

    2016-10-01

    Borophene, the boron atom analogue to graphene, being atomic thick have been just recently experimentally fabricated. In this work, we employ first-principles density functional theory calculations to investigate the interaction of Ca, Mg, Na or Li atoms with single-layer and free-standing borophene. We first identified the most stable binding sites and their corresponding binding energies as well and then we gradually increased the ions concentration. Our calculations predict strong binding energies of around 4.03 eV, 2.09 eV, 2.92 eV and 3.28 eV between the borophene substrate and Ca, Mg, Na or Li ions, respectively. We found that the binding energy generally decreases by increasing the ions content. Using the Bader charge analysis, we evaluate the charge transfer between the adatoms and the borophene sheet. Our investigation proposes the borophene as a 2D material with a remarkably high capacity of around 800 mA h/g, 1960 mA h/g, 1380 mA h/g and 1720 mA h/g for Ca, Mg, Na or Li ions storage, respectively. This study can be useful for the possible application of borophene for the rechargeable ion batteries.

  13. A novel pineapple-structured Si/TiO{sub 2} composite as anode material for lithium ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Yan, Dong; Bai, Ying; Yu, Caiyan; Li, Xiaoge; Zhang, Weifeng, E-mail: wfzhang6@163.com

    2014-10-01

    Highlights: • Pineapple-structured Si/TiO{sub 2} composite was firstly synthesized by a simple sol–gel method. • Pineapple-structured Si/TiO{sub 2} composite exhibits the best cycling stability. • TiO{sub 2} layer not only effectively inhibits the volume change of Si, but also contributes its electrochemical activity. - Abstract: Nanoscaled Si is successfully wrapped with different contents of nano-TiO{sub 2} (the molar ratios of Si/TiO{sub 2} composites are 1:1, 1:2, 1:3, 1:4 and 1:5, respectively) to form a novel pineapple structure. X-ray diffraction (XRD), Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), field emission scanning electron microscopy (FESEM) and high resolution transmission electron microscopy (HRTEM) are utilized to characterize the structure, component, chemical environment and morphology of the composite. The investigation in cycling performances demonstrates that Si/TiO{sub 2} with molar ratio of 1:4 exhibits the best cycling stability, with specific capacity of 593 mA h g{sup −1} after 50 cycles at 0.1 C, much higher than those of the other composites and the pristine material. Cyclic voltammetry (CV) profiles are also measured and compared. It is believed that the outside TiO{sub 2} particles act as buffer against the huge volume change of Si during repeated alloying and de-alloying, which explains the improved electrochemical performances.

  14. 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.

  15. Structural and electrochemical studies of a hexa phenylbenzene pyro lysed soft carbon as anode material in lithium batteries

    Energy Technology Data Exchange (ETDEWEB)

    Bonino, Franco [Chemistry Department, University ' La Sapienza' , P. le A. Moro 5, 00185 Rome (Italy)]. E-mail: bonino@uniromal.it; Brutti, Sergio [Chemistry Department, University ' La Sapienza' , P. le A. Moro 5, 00185 Rome (Italy); Piana, Michele [Chemistry Department, University ' La Sapienza' , P. le A. Moro 5, 00185 Rome (Italy); Natale, Sergio [Chemistry Department, University ' La Sapienza' , P. le A. Moro 5, 00185 Rome (Italy); Scrosati, Bruno [Chemistry Department, University ' La Sapienza' , P. le A. Moro 5, 00185 Rome (Italy); Gherghel, Lileta [Max-Planck Institute for Polymer Research, Ackermannweg 10, 55124 Mainz (Germany); Muellen, Klaus [Max-Planck Institute for Polymer Research, Ackermannweg 10, 55124 Mainz (Germany)

    2006-04-25

    XRD, Sem micrographs, Bet analyses and typical electrochemical experiments (cyclic voltammetry, step voltammetry and Li insertion/de insertion at constant current) have been carried out to characterize a new type of soft carbons obtained by pyrolysis of hexa phenylbenzene (Hb). By means of XRD and cyclic voltammetry at least three different type of sites for lithium storage were found. The first is graphite like type with d {sub 002} graph ene layer distance greater than pure graphite; the second is associated to disordered volumes among crystallities and the third is represented by Li sites at the hydrogen-terminated edges of hexagonal carbon fragments, characterized by higher energy in comparison with simple insertion sites. These last two types of sites are able to store some extra lithium, compared to pure graphite. BET analyses and cyclic voltammetries demonstrate the key role of the milling time on the characteristics and properties of this HPB pyrolysed carbon. Specific capacities shown by this pyrolysed material in Li coin-type cell have been also reported.

  16. 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

  17. Si clusters/defective graphene composites as Li-ion batteries anode materials: A density functional study

    Energy Technology Data Exchange (ETDEWEB)

    Li, Meng; Liu, Yue-Jie; Zhao, Jing-xiang, E-mail: zhaojingxiang@hrbnu.edu.cn; Wang, Xiao-guang, E-mail: hsdwsg@163.com

    2015-08-01

    Highlights: • We study the interaction between Si clusters with pristine and defective graphene. • We find that the binding strength of Si clusters on graphene can be enhanced to different degrees after introducing various defects. • It is found that both graphene and Si cluster in the Si/graphene composites can preserve their Li uptake ability. - Abstract: Recently, the Si/graphene hybrid composites have attracted considerable attention due to their potential application for Li-ion batteries. How to effectively anchor Si clusters to graphene substrates to ensure their stability is an important factor to determine their performance for Li-ion batteries. In the present work, we have performed comprehensive density functional theory (DFT) calculations to investigate the geometric structures, stability, and electronic properties of the deposited Si clusters on defective graphenes as well as their potential applications for Li-ion batteries. The results indicate that the interfacial bonding between these Si clusters with the pristine graphene is quietly weak with a small adsorption energy (<−0.21 eV). Due to the presence of vacancy site, the binding strength of Si clusters on defective graphene is much stronger than that of pristine one, accompanying with a certain amount of charge transfer from Si clusters to graphene substrates. Moreover, the ability of Si/graphene hybrids for Li uptake is studied by calculating the adsorption of Li atoms. We find that both graphenes and Si clusters in the Si/graphene composites preserve their Li uptake ability, indicating that graphenes not only server as buffer materials for accommodating the expansion of Si cluster, but also provide additional intercalation sites for Li.

  18. Si clusters/defective graphene composites as Li-ion batteries anode materials: A density functional study

    International Nuclear Information System (INIS)

    Highlights: • We study the interaction between Si clusters with pristine and defective graphene. • We find that the binding strength of Si clusters on graphene can be enhanced to different degrees after introducing various defects. • It is found that both graphene and Si cluster in the Si/graphene composites can preserve their Li uptake ability. - Abstract: Recently, the Si/graphene hybrid composites have attracted considerable attention due to their potential application for Li-ion batteries. How to effectively anchor Si clusters to graphene substrates to ensure their stability is an important factor to determine their performance for Li-ion batteries. In the present work, we have performed comprehensive density functional theory (DFT) calculations to investigate the geometric structures, stability, and electronic properties of the deposited Si clusters on defective graphenes as well as their potential applications for Li-ion batteries. The results indicate that the interfacial bonding between these Si clusters with the pristine graphene is quietly weak with a small adsorption energy (<−0.21 eV). Due to the presence of vacancy site, the binding strength of Si clusters on defective graphene is much stronger than that of pristine one, accompanying with a certain amount of charge transfer from Si clusters to graphene substrates. Moreover, the ability of Si/graphene hybrids for Li uptake is studied by calculating the adsorption of Li atoms. We find that both graphenes and Si clusters in the Si/graphene composites preserve their Li uptake ability, indicating that graphenes not only server as buffer materials for accommodating the expansion of Si cluster, but also provide additional intercalation sites for Li

  19. Si-Based Composite Anode Materials for Li-Ion Batteries%锂离子电池硅复合负极材料研究进展

    Institute of Scientific and Technical Information of China (English)

    高鹏飞; 杨军

    2011-01-01

    Silicon is one of the most attractive anode materials for lithium ion batteries on account of its low discharge potential and the highest theoretical capacity for lithium storage. However, the large volume effect, poor electronic conductivity and incompatibility with the conventional electrolyte hinder its commercial applications. So far, strategies to overcome these hinders include designing the composition and microstructure of silicon active materials to suppress the volume change and improve the conductivity, developing new binders and electrolyte additives and exploring new current collectors and suitable electrode structures. There are mainly two methods to improve the silicon active materials. One is to decrease the scale of active Si domain to nanoscale, the other is to fabricate the composite structures. This paper summarizes the recent progress in silicon based composite materials,including Si-nonmetal composites and Si-metal composites, as well as some researches of our group, and discusses the technological bottlenecks and development trends.%硅基负极材料具有最高的储锂容量和较低的电压平台,是最具潜力的下一代锂离子电池负极材料之一.然而,硅负极巨大的体积效应、较低的电导率以及与常规电解液的不相容性限制了其商业化应用.目前,提高硅负极性能的措施主要包括:通过设计硅基负极材料的组成和微观结构来抑制其体积变化并改善导电性,研发适于硅负极的粘结剂和电解液添加剂,探索新型集流体及电极结构等.其中改进活性硅基材料的主要措施有纳米化、复合化等.本文论述了近年来硅基复合材料研究领域的一些最新进展和研究热点,阐述了本课题组在此领域的一些工作;讨论了硅-非金属复合材料、硅-金属复合材料各自存在的技术瓶颈并展望其未来发展方向.

  20. 锂离子电池纳米级硅负极的研究进展%Research progress of nano-silicon based anode materials for lithium ion batteries

    Institute of Scientific and Technical Information of China (English)

    周向阳; 唐晶晶; 杨娟; 王松灿; 谢静

    2012-01-01

    硅基材料是新一代高容量锂离子电池负极材料的典型代表,近年来已成为理论和应用研究的热点.纳米硅基负极材料因具有独特的表面效应和尺寸效应等优点,可大大改善硅作为负极时所存在的循环性能,有望解决限制硅负极成为替代商业化石墨负极的瓶颈问题.介绍了近年来纳米级硅负极作为锂离子电池负极材料的最新研究进展,包括纳米硅颗粒、硅纳米线、硅纳米管及纳米硅薄膜,分析了纳米硅作为锂离子电池负极材料存在的问题,总结了纳米级硅作为锂离子电池负极较为可行的研究方法,展望了纳米硅作为高能量密度锂离子电池负极材料的研究前景.%Silicon-based materials have been extensively studied as the typical representation of high capacity anode materials in lithium-ion batteries. Nano-silicon based anodes have been investigated as possible substitute for the commercial graphite or carbon due to their unique surface effect and size effect. The nano-silicon based anode materials in recent years were reviewed, including nano-silicon powder, silicon nanowires, silicon nanotubes and nanosized silicon thin film. The prospects for high energy density lithium ion batteries anode materials were also discussed. The feasible research methods for the nanoscale silicon as anode materials were summarized. The new material for lithium-ion batteries would be promising if some problems can be solved.

  1. Enhanced electrochemical performance of Li4Ti5O12 as anode material for lithium-ion batteries with different carbons as support

    International Nuclear Information System (INIS)

    Nano-Li4Ti5O12/carbon composites with various structures are designed using tetrabutyl titanate as a precursor via a facile in situ liquid deposition method in the presence of three different carbons (multiwalled carbon nanotubes, spherical conductive carbon black super-P and ordered macroporous carbon). The nano-Li4Ti5O12/carbon composites with various morphologies are formed depending on the carbon matrixes used. The Li4Ti5O12 particles obtained are approximately 100 nm in size and homogeneously dispersed in different carbon matrixes. It is found that the structures of the carbon matrixes have a close relation to the discharge capacities of the composites. At the discharge current density of 875 mA g−1, the discharge capacities of nano-Li4Ti5O12/carbon composites with 10 wt% carbon are 138.6, 120.8 and 120.9 mAh g−1 for carbon nanotubes, super-P and porous carbon as the carbon supports, respectively. The nano-Li4Ti5O12/carbon using carbon nanotubes as support exhibits superior performance with large reversible capacity, excellent cycle stability and good rate capability. Capacity retention of 99% can be maintained after 100 cycles, suggesting its promising potential as anode materials. - Highlights: • Li4Ti5O12/carbon nanocomposites are designed using different carbons as supports. • Li4Ti5O12 particles formed on carbon matrix are fine and homogeneous. • Aggregation and growth of Li4Ti5O12 particles are inhibited. • The Li4Ti5O12/carbon nanocomposites exhibit superior electrochemical performance

  2. High rate capability and long cycle stability of TiO{sub 2−δ}–La composite nanotubes as anode material for lithium ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Jiwei; Zhang, Jingwei, E-mail: jwzhang@henu.edu.cn; Ren, Huanhuan; Yu, Laigui; Wu, Zhishen; Zhang, Zhijun, E-mail: zhangzhijun@henu.edu.cn

    2014-10-01

    Highlights: • TiO{sub 2−δ}–La composite nanotubes were synthesized. • Nanotubular morphology destruction is alleviated during the heat-treatment process. • Mixed Ti{sup 4+}/Ti{sup 3+} valence is generated. • As a result, the composite shows excellent rate capability and cyclability. - Abstract: TiO{sub 2−δ}–La composite nanotubes are prepared by heating the ethanol solution of La(NO{sub 3}){sub 3}⋅6H{sub 2}O which is introduced into nanotube titanium acid at pre-set temperature. The effect of La dosage on the microstructure and electrochemical properties of as-fabricated TiO{sub 2−δ}–La composite nanotubes is investigated. Results indicate that La{sup 3+} can be trapped in the internal/external surfaces and the interlayer space of nanotubes. All of these help to retain the nanotubular morphology and layered structure during the dehydration process. Ti{sup 3+} defects generated by the dehydration of nanotube titanium acid can be stabilized by the formed Ti–O–La bond. So, as-fabricated TiO{sub 2−δ}–La composite nanotubes samples exhibit markedly improved electrochemical properties than pristine TiO{sub 2}. Particularly, the electrode made of TiO{sub 2−δ}–La composite nanotubes containing 5% La element (mass fraction) has a high capacity of 142 mA h g{sup −1} at a charge/discharge rate of 20 C rate and a capacity retention of 87% after 1000 cycles at 10 C, showing superior electrochemical performance and great potential as an anode material for high-rate lithium-ion batteries.

  3. Synthesis and electrochemical performances of ZnO/MnO2 sea urchin-like sleeve array as anode materials for lithium-ion batteries

    International Nuclear Information System (INIS)

    MnO2 is electrodeposited onto ZnO nanorod array grown on Ni foil, forming a binder-free ZnO/MnO2 composited electrode. XRD, EDS, SEM and TEM are used to analyze the phase and microstructure of this composite. Burr-like MnO2 nanoflakes grows on ZnO nanorod array, the top of the composite is hollow and at the bottom exists ZnO large block core as an internal support, forming ZnO/MnO2 sea urchin-like sleeve array. As anode material for lithium ion batteries, ZnO/MnO2 sleeve array exhibits higher discharge capacity and coulombic efficiency, better rate performance and cycling stability than single ZnO nanorod array or directly electrodepsited MnO2, and the composite effect is very remarkable. After 100 cycles, the discharge capacity of ZnO/MnO2 still reaches 1259 mA h g−1, and coulombic efficiency surpasses 98%, higher than those of ZnO nanorod array (111 mA h g−1) and directly electrodeposited MnO2 (507 mA h g−1). The improvement of the electrochemical performances is due to the unique sea urchin-like sleeve array architecture. MnO2 burr tube shell structure leads to high electrochemical activity while the internal ZnO core support ensures good structure stability. The gradually opening of sea urchin-like sleeve during the cycling further enhances the electrochemical activity of MnO2, stabilizing and increasing electrochemical performances of the ZnO/MnO2 composite

  4. High rate capability of TiO{sub 2}/nitrogen-doped graphene nanocomposite as an anode material for lithium–ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Cai, Dandan; Li, Dongdong; Wang, Suqing [School of Chemistry and Chemical Engineering, South China University of Technology, Wushan Road, Guangzhou (China); Zhu, Xuefeng; Yang, Weishen [State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian (China); Zhang, Shanqing [Centre for Clean Environment and Energy, Environmental Futures Centre and Griffith School of Environment, Gold Coast Campus, Griffith University, QLD 4222 (Australia); Wang, Haihui, E-mail: hhwang@scut.edu.cn [School of Chemistry and Chemical Engineering, South China University of Technology, Wushan Road, Guangzhou (China)

    2013-06-05

    Highlights: ► TiO{sub 2}/N-doped graphene composite was synthesized by a gas/liquid interfacial method. ► The nanocomposite was used to fabricate lithium-ion batteries. ► Its electrochemical performance was evaluated for the first time. ► The anode material exhibits a good cycling performance and rate capability. -- Abstract: TiO{sub 2}/nitrogen-doped graphene nanocomposite was synthesized by a facile gas/liquid interface reaction. The structure and morphology of the sample were analyzed by X-ray diffraction analysis, X-ray photoelectron spectroscopy, scanning electron microscopy and transmission electron microscopy. The results indicate that nitrogen atoms were successfully doped into graphene sheets. The TiO{sub 2} nanoparticles (8–13 nm in size) were homogenously anchored on the nitrogen-doped graphene sheets through gas/liquid interface reaction. The as-prepared TiO{sub 2}/nitrogen-doped graphene nanocomposite shows a better electrochemical performance than the TiO{sub 2}/graphene nanocomposite and the bare TiO{sub 2} nanoparticles. TiO{sub 2}/nitrogen-doped graphene nanocomposite exhibits excellent cycling stability and shows high capacity of 136 mAh g{sup −1} (at a current density of 1000 mA g{sup −1}) after 80 cycles. More importantly, a high reversible capacity of 109 mAh g{sup −1} can still be obtained even at a super high current density of 5000 mA g{sup −1}. The superior electrochemical performance is attributed to the good electronic conductivity introduced by the nitrogen-doped graphene sheets and the positive synergistic effect between nitrogen-doped graphene sheets and TiO{sub 2} nanoparticles.

  5. Microwave irradiation synthesis of Co3O4 quantum dots/graphene composite as anode materials for Li-ion battery

    International Nuclear Information System (INIS)

    Graphical abstract: - Highlights: • Co3O4 quantum dots/graphene composites are fabricated via microwave irradiation method. • Uniform Co3O4 nanocrystals of 3-8 nm are homogeneously dispersed on graphene nanosheets. • Reversible capacity of the composite retains 1785 mAh g−1 after 90 cycles at 0.1 C. • Co3O4 quantum dots/graphene can tolerate high current cycling and have good retention of capacity. • Enhanced performances could result from quantum and size effects of quantum dots. - Abstract: Co3O4 quantum dots/graphene composites were synthesized by a facile and efficient microwave irradiation method, and they were analyzed using XRD, TEM, HRTEM, and TG. Uniform Co3O4 nanocrystals of about 3-8 nm with a high density are homogeneously dispersed on graphene nanosheets. When used as anode materials for Li-ion batteries, the Co3O4 quantum dots/graphene composites show a significantly enhanced cycling performance (1785 mAh g−1 at 0.1 C after 90 cycles) as well as high rate capability (485 mAh g−1 at 5 C). The reversible capacity is found to be much higher than the theoretical value. The superior performance could be attributed to the interfacial lithium-storage and the quantum and size effects of quantum dots that lead to high activity during the lithiation/delithiation process. In addition, the flexible and conductive graphene nanosheets and well dispersed Co3O4 nanodots as well as the synergetic effect between them also benefit the electrochemical performance by endowing a superior high surface area and shortening the diffusion pathway of lithium ions

  6. Cu0.02Ti0.94Nb2.04O7: An advanced anode material for lithium-ion batteries of electric vehicles

    Science.gov (United States)

    Yang, Chao; Lin, Chunfu; Lin, Shiwei; Chen, Yongjun; Li, Jianbao

    2016-10-01

    To explore advanced anode materials for lithium-ion batteries of electric vehicles, Cu2+/Nb5+ co-doped TiNb2O7 is studied. Cu0.02Ti0.94Nb2.04O7 is successfully fabricated using a facile solid-state reaction. X-ray diffraction analyses combined with Rietveld refinements demonstrate that the trace Cu2+/Nb5+ co-doping does not destroy the shear ReO3 crystal structure of TiNb2O7 but increases the lattice parameters and unit cell volume. Specific surface area tests and scanning electron microscopy images reveal a smaller average particle size in Cu0.02Ti0.94Nb2.04O7. Due to the increased unit cell volume and free 3d electrons in Cu2+ ions, the Li+-ion diffusion coefficient and electronic conductivity of Cu0.02Ti0.94Nb2.04O7 are respectively enhanced by 14.8 times and at least 220 times. Consequently, Cu0.02Ti0.94Nb2.04O7 exhibits advanced electrochemical properties in terms of specific capacity, rate capability and cyclic stability. At 0.1 C, it delivers a large first-cycle discharge/charge capacity of 346/315 mAh g-1. At 10 C, it still provides a large capacity of 182 mAh g-1 with tiny loss of only 1.2% over 1000 cycles. In sharp contrast, TiNb2O7 shows a small capacity of only 90 mAh g-1 and large loss of 59.8%. Therefore, Cu0.02Ti0.94Nb2.04O7 possesses great potential for the application in lithium-ion batteries for electric vehicles.

  7. Highly redox-resistant solid oxide fuel cell anode materials based on La-doped SrTiO3 by catalyst impregnation strategy

    Science.gov (United States)

    Shen, X.; Sasaki, K.

    2016-07-01

    An anode backbone using 40 wt% (ZrO2)0.89(Sc2O3)0.1(CeO2)0.01 (SSZ)-Sr0.9La0.1TiO3 (SLT) cermet was prepared for SSZ electrolyte-supported SOFC single cells. 15 mgcm-2 Ce0.9Gd0.1O2 (GDC) was impregnated to totally cover the SSZ-SLT anode backbone surface acting as a catalyst, and the cell voltage achieved 0.865 V at 200 mAcm-2 using (La0.75Sr0.25)0.98MnO3 (LSM)-SSZ cathode in 3%-humidified hydrogen fuel at 800 °C. Cell performance was substantially improved from 0.865 V to >0.97 V when 0.03 mgcm-2 Pd or Ni was further incorporated as a secondary catalyst into the anode layer. 50 redox cycles were performed to investigate redox stability of this high performance anode. It was found that even after the 50 redox cycle long-term degradation test, cell voltage at 200 mAcm-2 was retained around 0.94 V, higher than the cell performance using the conventional Ni-SSZ cermet anode. The catalytically-active reaction sites at ceria-Pd or ceria-Ni may account for the excellent performance, and the extremely low metal catalyst concentration prevent serious metal aggregation in achieving excellent redox stability.

  8. Nickel and nitrogen co-doped tin dioxide nano-composite as a potential anode material for lithium-ion batteries

    International Nuclear Information System (INIS)

    Highlights: • Ni and N co-doped SnO2 nano-composite was prepared for the first time. • The co-doped material exhibits the optimal electrochemical performances. • The co-doping increases the grain size, surface area, pore diameter and conductivity. • The accelerated electrode kinetics has been observed, explored and explained. - Abstract: As a promising high capacity anode material for lithium-ion batteries (LIBs), tin dioxide (SnO2) has attracted considerable interest in recent studies. In this paper, nickel-doped tin dioxide (Ni/SnO2), nickel and nitrogen co-doped tin dioxide (Ni-N/SnO2) are prepared to modify the electrochemical properties of as-prepared SnO2. Samples of pure SnO2, Ni/SnO2 and Ni-N/SnO2 are characterized by X-ray diffraction (XRD), field-emission scanning electron microscopy (FESEM) and high resolution transmission electron microscopy (HRTEM), energy dispersive X-ray analysis (EDAX), Raman spectroscopy, X-ray photoelectron spectroscopy (XPS) and Brunauer-Emmett-Teller (BET). It is found that doping and co-doping process does not affect the phase structure of pristine SnO2. However, it obviously influences the morphology, specific surface area, and electrochemical properties of SnO2. Gavalnostatic cycling indicates that the Ni-N/SnO2 nano-composite still remains a high charge capacity of 631 mAh g−1 after 50 cycles. Rate performance evaluation shows that a capacity of 621 mAh g−1 can still be delivered when the current returns back to 0.1 C after 50 cycles at different current densities. Cyclic voltammetry (CV) analysis proves that Ni and N co-doping accelerates the electrode reaction. The results of electrochemical impedance spectroscopy (EIS) demonstrate the low charge-transfer resistance for Ni-N/SnO2, and the following quantitative calculation further confirms the highest electric conductivity and ionic conductivity of Ni-N/SnO2 compared with those of pure SnO2 and Ni/SnO2. This explains the superior capacity retention and rate

  9. 锂离子电池硅基负极改性研究新进展%Research Progress in Silicon Based Anode Materials for Lithium-ion Batteries

    Institute of Scientific and Technical Information of China (English)

    邹幽兰; 杨娟; 周向阳; 唐晶晶; 王松灿; 谢静

    2011-01-01

    Due to its high capacity,silicon based anode materials have been widely studied in recent years. The insertion/interinsertion lithium-ion principle of silicon anode for lithium-ion battery is mainly analyzed, the latest allevi ation methods of cracking and crushing of the silicon are reviewed, and the shortcoming of these methods is also pre sented. With the advantage of high conductivity,high elastic, porous, high stability, polypyrrole compouded with sili con will be the most promising developing direction to improve the cycle stability of silicon-based anode materials in lithium-ion battery.%硅因其具有极高的理论容量而成为现阶段锂离子电池用负极材料研究的热点.介绍了硅基负极材料嵌/脱锂的原理,总结了目前缓解硅开裂与粉碎的一般方法,分析了现行研究中的不足.聚吡咯具有高导电性、高弹性、多孔、高稳定性等优点,为了提高负极材料循环稳定性能,将其与硅结舍得到的Si-PPy复合材料将是最有希望的发展方向.

  10. Releasing metal catalysts via phase transition: (NiO)0.05-(SrTi0.8Nb0.2O3)0.95 as a redox stable anode material for solid oxide fuel cells.

    Science.gov (United States)

    Xiao, Guoliang; Wang, Siwei; Lin, Ye; Zhang, Yanxiang; An, Ke; Chen, Fanglin

    2014-11-26

    Donor-doped perovskite-type SrTiO3 experiences stoichiometric changes at high temperatures in different Po2 involving the formation of Sr or Ti-rich impurities. NiO is incorporated into the stoichiometric strontium titanate, SrTi0.8Nb0.2O3-δ (STN), to form an A-site deficient perovskite material, (NiO)0.05-(SrTi0.8Nb0.2O3)0.95 (Ni-STN), for balancing the phase transition. Metallic Ni nanoparticles can be released upon reduction instead of forming undesired secondary phases. This material design introduces a simple catalytic modification method with good compositional control of the ceramic backbones, by which transport property and durability of solid oxide fuel cell anodes are largely determined. Using Ni-STN as anodes for solid oxide fuel cells, enhanced catalytic activity and remarkable stability in redox cycling have been achieved. Electrolyte-supported cells with the cell configuration of Ni-STN-SDC anode, La0.8Sr0.2Ga0.87Mg0.13O3 (LSGM) electrolyte, and La0.6Sr0.4Co0.2Fe0.8O3 (LSCF) cathode produce peak power densities of 612, 794, and 922 mW cm(-2) at 800, 850, and 900 °C, respectively, using H2 as the fuel and air as the oxidant. Minor degradation in fuel cell performance resulted from redox cycling can be recovered upon operating the fuel cells in H2. Such property makes Ni-STN a promising regenerative anode candidate for solid oxide fuel cells.

  11. Bio-Inspired Hierarchical Nanofibrous Fe3O4-TiO2-Carbon Composite as a High-Performance Anode Material for Lithium-Ion Batteries.

    Science.gov (United States)

    Li, Shun; Wang, Mengya; Luo, Yan; Huang, Jianguo

    2016-07-13

    A bioinspired hierarchical nanofibrous Fe3O4-TiO2-carbon composite was fabricated by employing natural cellulose substance (e.g., filter paper) as both the scaffold and the carbon source and showed improved electrochemical performances when it is employed as an anode material for lithium-ion batteries. FeOOH nanoparticles were first grown uniformly onto the surface of the titania thin-layer precoated cellulose nanofibers, and thereafter, the as-prepared FeOOH-TiO2-cellulose composite was calcined and carbonized in argon atmosphere at 500 °C for 6 h to produce the Fe3O4-TiO2-carbon composite. The resultant composite possesses a hierarchical structure that was faithfully inherited from the initial cellulose substance, which was composed of titania-coated carbon fibers with corncob-like shaped Fe3O4 nanoparticles immobilized on the surfaces. The diameter of the composite nanofiber is ca. 100-200 nm, and the diameter of the Fe3O4 nanoparticle is about 30 nm, which is coated with an ultrathin carbon layer with a thickness about 3 nm. This composite displayed superior lithium-ion storage performance. It showed a first-cycle discharge capacity of 1340 mAh/g, delivering a stable reversible capacity of ca. 525 mAh/g after 100 charge-discharge cycles at a current density of 100 mA/g, and the efficiency is as high as ca. 95% of the theoretical value. This is much higher than those of the commercial Fe3O4 powder (160 mAh/g) and the Fe3O4-carbon counter material (310 mAh/g). It was demonstrated that the thin titania precoating layer (thickness ca. 3-5 nm) is necessary for the high content loading of the Fe3O4 nanoparticles onto the carbon nanofibers. Owing to the unique three-dimensional porous network structure of the carbon-fiber scaffold, together with the ultrathin outer carbon-coating layer, the composite showed significantly improved cycling stability and rate capability.

  12. International comparison of Cd content in a quality control material of Navajuelas (Tagelus dombeii) determined by anodic stripping voltammetry, atomic absorption spectrometry and neutron activation analysis

    Energy Technology Data Exchange (ETDEWEB)

    Queirolo, F. (Universidad Catolica del Norte, Antofagasta (Chile). Dept. of Chemistry Forschungszentrum Juelich GmbH (Germany, F.R.). Inst. fuer Angewandte Physikalische Chemie Universidad de Extremadura, Badajoz (Spain). Dept. of Analytical Chemistry and Electrochemistry); Ostapczuk, P. (Forschungszentrum Juelich GmbH (Germany, F.R.). Inst. fuer Angewandte Physikalische Chemie); Valenta, P.; Stegen, S. (Forschungszentrum Juelich GmbH (Germany, F.R.). Inst. fuer Angewandte Physikalische Chemie Universidad de Extremadura, Badajoz (Spain). Dept. of Analytical Chemistry and Electrochemistry); Marin, C.; Vinagre, F.; Sanchez, A. (Universidad de Extremadura, Badajoz (Spain). Dept. of Analytical Chemistry and Electrochemistry)

    1991-05-01

    The determination of Cd was performed by neutron activation analysis (NAA), atomic absorption spectrometry (AAS) with flame or in the electrothermal mode and anodic stripping voltammetry in the differential pulse mode (DPASV) and the square wave mode (SWASV). (orig./EF).

  13. Lithium Ion Battery Anode Aging Mechanisms

    Directory of Open Access Journals (Sweden)

    Victor Agubra

    2013-03-01

    Full Text Available Degradation mechanisms such as lithium plating, growth of the passivated surface film layer on the electrodes and loss of both recyclable lithium ions and electrode material adversely affect the longevity of the lithium ion battery. The anode electrode is very vulnerable to these degradation mechanisms. In this paper, the most common aging mechanisms occurring at the anode during the operation of the lithium battery, as well as some approaches for minimizing the degradation are reviewed.

  14. 锂离子电池C-Sn-金属复合负极材料的研究进展%Research Progress of C-Sn-alloy Composite Anode Materials for Li-ion Batteries

    Institute of Scientific and Technical Information of China (English)

    王录娥; 任旭梅; 吴峰

    2011-01-01

    The development status of carbon and tin-alloy composite anode materials is introduced. C-Sn com posite materials are classified into three categories, and the electrochemical performance characteristics for every type of composite materials are analysed. The latest progress of C-Sn-alloy composite materials, which have a higher capaci ty and excellent cycle performance is outlined. Therefore, it is a promising anode material for Li-ion batteries in the future.%综述了锂离子电池碳材料与锡基合金复合材料的发展现状,总结了C-Sn二元复合材料的主要种类,并分析了它们作为负极材料的电化学性能特点;同时阐述了C-Sn-金属三元复合材料的发展,这种复合材料结合了碳材料的循环稳定性和合金材料的高比容量的优势,是具有发展前景的新型锂离子电池负极材料.

  15. The Temperature Stage Which Used At Anode Paste Doughing Process In Green Plant PT Inalum

    OpenAIRE

    Simatupang, Dian Christian

    2011-01-01

    Anode is raw material which used in electrolyse process aluminium smelting, where anode is form mixed of cokes and coal tar pitch, containing carbon element which required in smelting process of alumina to produce aluminium. PT INALUM has been able to produce anode it self, while cathode is still be imported from other countries. Aluminium smelter process which taking place continiously require many of anode, good quality and durable, especially temperature at doughing process of anode paste ...

  16. Study of Sr2Mg(Mo0.8Nb0.2)O6-δ as anode material for solid oxide fuel cells using hydrocarbons as fuel

    Science.gov (United States)

    Escudero, M. J.; Gómez de Parada, I.; Fuerte, A.; Daza, L.

    2013-12-01

    Sr2Mg(Mo0.8Nb0.2)O6-δ (SMMNb) was investigated as potential anode material of solid oxide fuel cells (SOFCs) for direct oxidation of methane. The compound was prepared by solid state reaction, followed by annealing under reducing atmosphere of 10% H2/N2 at 900 °C. The structural and morphological properties of fresh and reduced material were characterized by XRD, XPS and SEM. Additionally, catalytic properties towards oxidation of methane, electrical properties in reducing atmosphere as well as thermal and chemical compatibility with common SOFC electrolytes were investigated. These results reveal a double perovskite single phase in the fresh and reduced compound and, after reduction, a change in the niobium valence was observed. SMMNb shows a good activity for methane partial oxidation as well as combined reforming reaction. The material presents a semiconductor behaviour with n-type electronic conduction and an excellent thermal compatibility with SOFC electrolytes such as SDC, GDC and LSGM, based on similarity of values of TEC. However, this material reacts with zirconia-based electrolytes (YSZ and ScSZ). Although, a low electrochemical activity for H2 and CH4 oxidation was found, SMMNb demonstrates high tolerance to carbon deposition when the anode is exposed to methane.

  17. 锂离子电池中石墨烯基金属氧化物负极材料的制备和应用%Preparation and application of lithium ion batteries graphene-based metal oxide anode materials

    Institute of Scientific and Technical Information of China (English)

    黄磊; 张艳华; 涂铭旌

    2014-01-01

    石墨烯是一种单原子层厚度的石墨材料,具有良好的电学、力学和热学性质。其作为锂离子电池电极材料时,能有效提高各项电化学性能,具有良好的应用前景。综述了锂离子电池中石墨烯基金属氧化物负极材料的制备方法,及石墨烯薄片和金属氧化物之间不同的复合结构和强烈的协同作用对提高石墨烯基负极材料电化学性能的作用。%Graphene was a single atomic layer thickness of graphite material,with good electrical,mechanical and thermal properties.When it was used as the electrode materials for lithium ion batteries,could effectively improve the various electrochemical performance,and it had a good application prospect.This paper summa-rized the preparation method of anode material of metallic oxide based graphene in the lithium ion battery,and different composite structure between graphene nanosheets and metal oxide,the structure had strong synergis-tic effect in improving the electrochemical performance of anode material of metallic oxide based graphene.

  18. 锂离子电池Si/C复合负极材料研究进展%Research progress of Si/C composite anode materials for lithium ion batteries

    Institute of Scientific and Technical Information of China (English)

    刘传永; 彭瑛; 刘建华

    2013-01-01

    硅和碳复合成锂离子电池复合负极材料,不但解决了碳容量低和硅体积效应大的问题,而且得到综合了碳循环性好和硅容量高特点的负极材料.综述了Si/C复合材料的类型和制备方法,提出了Si/C复合材料未来发展方向.%Silicon and carbon were composited as Si/C composite anode materials for lithium ion batteries,which not only solved the problems that carbon has low capacity of and silicon has big volume affection,but also got the anode materials that integrated the good cycle of carbon with high capacity of silicon.The types and preparation methods of Si/C composite materials were reviewed and the future development direction of Si/C composite materials was raised.

  19. Highly efficient and scalable synthesis of SiOx/C composite with core-shell nanostructure as high-performance anode material for lithium ion batteries

    International Nuclear Information System (INIS)

    Highlights: • Highly efficient and scalable colloidal route was employed to synthesize SiOx/C. • Nanosized SiOx/C composite has core-shell structure with a thinner carbon layer. • The SiOx/C composite shows a low x value (O/Si ratio) of ca. 0.88. • High specific capacity, good cycleability and superior rate-capability are achieved. - Abstract: SiOx-based electrodes have shown great potential as lithium ion battery anodes because of their high specific capacity. Nonetheless, synthesis of SiOx-based anodes in an industrially adaptable scale still remains as a great challenge. Herein, we adopt a highly efficient colloidal route to enable scalable and high yield synthesis of core-shell SiOx/C composite. The prepared SiOx/C composite presents a well-distributed nanostructure composing of SiOx nanoparticles coated with a thinner carbon layer. The electrode delivers a stable reversible capacity of ca. 820 mAh g−1 over 100 cycles, and exhibits excellent rate capability. The nano-scale feature of SiOx and the coating carbon layer ensure the excellent electrochemical performance of SiOx/C. The approach is facile, mild and mass-productive, which can be adopted for tunable large-scale production of high-capacity SiOx/C composite anode

  20. Microscopical characterization of carbon materials derived from coal and petroleum and their interaction phenomena in making steel electrodes, anodes and cathode blocks for the Microscopy of Carbon Materials Working Group of the ICCP

    Science.gov (United States)

    Predeanu, G.; Panaitescu, C.; Bălănescu, M.; Bieg, G.; Borrego, A.G.; Diez, M. A.; Hackley, Paul C.; Kwiecińska, B.; Marques, M.; Mastalerz, Maria; Misz-Kennan, M.; Pusz, S.; Suarez-Ruiz, I.; Rodrigues, S.; Singh, A. K.; Varma, A. K.; Zdravkov, A.; Zivotić, D.

    2015-01-01

    This paper describes the evaluation of petrographic textures representing the structural organization of the organic matter derived from coal and petroleum and their interaction phenomena in the making of steel electrodes, anodes and cathode blocks.This work represents the results of the Microscopy of Carbon Materials Working Group in Commission III of the International Committee for Coal and Organic Petrology between the years 2009 and 2013. The round robin exercises were run on photomicrograph samples. For textural characterization of carbon materials the existing ASTM classification system for metallurgical coke was applied.These round robin exercises involved 15 active participants from 12 laboratories who were asked to assess the coal and petroleum based carbons and to identify the morphological differences, as optical texture (isotropic/anisotropic), optical type (punctiform, mosaic, fibre, ribbon, domain), and size. Four sets of digital black and white microphotographs comprising 151 photos containing 372 fields of different types of organic matter were examined. Based on the unique ability of carbon to form a wide range of textures, the results showed an increased number of carbon occurrences which have crucial role in the chosen industrial applications.The statistical method used to evaluate the results was based on the “raw agreement indices”. It gave a new and original view on the analysts' opinion by not only counting the correct answers, but also all of the knowledge and experience of the participants. Comparative analyses of the average values of the level of overall agreement performed by each analyst in the exercises during 2009–2013 showed a great homogeneity in the results, the mean value being 90.36%, with a minimum value of 83% and a maximum value of 95%.

  1. Battery, especially for portable devices, has an anode containing silicon

    OpenAIRE

    S. Y. Kan

    2002-01-01

    The anode (2) contains silicon. A battery with a silicon-containing anode is claimed. An Independent claim is also included for a method used to make the battery, comprising the doping of a silicon substrate (1) with charge capacity-increasing material (preferably boron, phosphorous or arsenic), etching the doped substrate layer in order to increase its porosity, and applying a cathode (3) in the form of a lithium oxide compound onto the resulting anode and applying an electrolyte (4) to the ...

  2. 植物碳化材料做电极用于生物电解产氢研究%Hydrogen Production from Microbial Electrolysis Cell Using Carbonized Plant Material as Anode

    Institute of Scientific and Technical Information of China (English)

    蔡储昊; 王秋辰; 罗丽雯; 徐苏云

    2016-01-01

    利用微生物电解池处理废水,可同步实现再生氢能源回收。本文将天然植物碳化处理后得到的材料作为微生物电解池的阳极,并探究不同植物原料对电解池产氢效率的影响。实验选取玉米棒、杏鲍菇和木屑作为原材料,通过高温管式炉焙烧碳化,扫描电镜观察发现三种植物在碳化处理后,呈现出不同特征的三维多孔结构。将这些碳化材料应用于微生物电解制氢,通过观测微生物电解池的电流变化趋势、产氢效率以及底物降解效率来对比材料性能。综合分析表明,玉米棒作为电极原材料是最合适的,它在碳化后形成的三维多孔结构适合微生物附着,也具备较好的导电性能,从而可以促进微生物电解池产氢。%Microbial electrolysis cell ( MEC ) is capable of producing hydrogen as a kind of clean energy and accomplishing wastewater treatment simultaneously. The present study utilized the carbonized plant materials as the anodes of MEC, and evaluated the influence of different raw materials on hydrogen production efficiency in MEC. Different natural macroporous carbon MEC electrodes were fabricated from corn stem, king mushroom and sawdust. After simple carbonization in tube furnace, these three natural materials presented their unique three-dimensional porous structures. These natural materials were then used as anodes in MEC system for hydrogen production. Three materials were compared in terms of current generation tendency, hydrogen production and substrate degradation efficiencies. Results showed that the carbon material derived from corn stem was the most suitable material, because bacteria can easily adhere to its three-dimensional porous structure, which made electron transfer more efficiently between bacteria and anode and thus promote the hydrogen production of MEC system.

  3. Mechanically stable insoluble titanium-lead anodes for sulfate electrolytes

    Directory of Open Access Journals (Sweden)

    Chmiola J.

    2003-01-01

    Full Text Available Different formulations of a new material to be used as an insoluble anode for copper electrowinning, a Ti-Pb composite, were investigated for both mechanical and electrochemical properties. Mechanical and metallographic characteristic tests, as well as short-term deposition tests were used to study the effect of the Ti/Pb ratio on anode performance. Yield strength and elastic modulus, obtained through tensile testing, significantly exceed that of lead. Metallographic procedures were used to assess the uniformity of lead distribution in the material, as well as porosity, which would be decreased below 1 % for most of the compositions under study. Short-term deposition tests were used to determine power consumption, deposit quality current efficiency and weight loss characteristics of the new anode material. The material with only 30 vol.% lead shows approximately the same electrochemical performance as a pure lead anode, but has much higher mechanical properties which prevent warping and extend the lifetime of the anode.

  4. Nano-sized Li-Fe composite oxide prepared by a self-catalytic reverse atom transfer radical polymerization approach as an anode material for lithium-ion batteries

    International Nuclear Information System (INIS)

    A novel Self-catalytic Reverse Atom Transfer Radical Polymerization (RATRP) approach that can provide the radical initiator and the catalyst by the system itself is used to synthesize a nano-sized Li-Fe composite oxide powder in large scale. Its crystalline structure and morphology have been characterized by X-ray diffraction and scanning electron microscopy. The results reveal that the composite is composed of nano-sized LiFeO2 and Fe3O4. Its electrochemical properties are evaluated by charge/discharge measurements. The results show that the Li-Fe composite oxide is an excellent anode material for lithium-ion batteries with good cycling performance (1249 mAh g-1 at 100th cycle) and outstanding rate capability (967 mAh g-1 at 5 C). Such a self-catalytic RATRP approach provides a way to synthesize nano-sized iron oxide-based anode materials industrially with preferable electrochemical performance and can also be applied in other polymer-related area.

  5. Redox Stable Anodes for Solid Oxide Fuel Cells

    Directory of Open Access Journals (Sweden)

    Guoliang eXiao

    2014-06-01

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

  6. Fundamental Investigation of Si Anode in Li-Ion Cells

    Science.gov (United States)

    Wu, James J.; Bennett, William R.

    2012-01-01

    Silicon is a promising and attractive anode material to replace graphite for high capacity lithium ion cells since its theoretical capacity is approximately 10 times of graphite and it is an abundant element on earth. However, there are challenges associated with using silicon as Li-ion anode due to the significant first cycle irreversible capacity loss and subsequent rapid capacity fade during cycling. In this paper, cyclic voltammetry and electrochemical impedance spectroscopy are used to build a fundamental understanding of silicon anodes. The results show that it is difficult to form the SEI film on the surface of Si anode during the first cycle, the lithium ion insertion and de-insertion kinetics for Si are sluggish, and the cell internal resistance changes with the state of lithiation after electrochemical cycling. These results are compared with those for extensively studied graphite anodes. The understanding gained from this study will help to design better Si anodes.

  7. A-site deficient La0.2Sr0.7TiO3-δ anode material for proton conducting ethane fuel cell to cogenerate ethylene and electricity

    Science.gov (United States)

    Liu, Subiao; Behnamian, Yashar; Chuang, Karl T.; Liu, Qingxia; Luo, Jing-Li

    2015-12-01

    A site deficient La0.2Sr0.7TiO3-δ (LSTA) and a highly proton conductive electrolyte BaCe0.7Zr0.1Y0.2O3-δ (BCZY) are synthesized by using solid state reaction method. The performance of the electrolyte-supported single cell, comprised of LSTA + Cr2O3 + Cu//BCZY//(La0.60Sr0.40)0.95Co0.20Fe0.80O3-δ (LSCF)+BCZY, is fabricated and investigated. LSTA shows remarkably high electrical performance, with a conductivity as high as 27.78 Scm-1 at 1150 °C in a 10% H2/N2 reducing atmosphere. As a main anode component, it shows good catalytic activity towards the oxidation of ethane, causing the power density to considerably increase from 158.4 mW cm-2 to 320.9 mW cm-2 and the ethane conversion to significantly rise from 12.6% to 30.9%, when the temperature increases from 650 °C to 750 °C. These changes agree well with the polarization resistance which dramatically decreases from 0.346 Ωcm2 to 0.112 Ωcm2. EDX measurement shows that no element diffusion exists (chemical compatibility) between anode (LSTA + Cr2O3+Cu) and electrolyte (BCZY). With these properties, the pure phase LSTA is evaluated as a high electro-catalytic activity anode material for ethane proton conducting solid oxide fuel cell (PC-SOFC).

  8. Development of Planar Metal Supported SOFC with Novel Cermet Anode

    DEFF Research Database (Denmark)

    Blennow Tullmar, Peter; Hjelm, Johan; Klemensø, Trine;

    2009-01-01

    SOFC, electrode material from the active anode layer may interdiffuse with the metallic support during sintering. The purpose of this work is to illustrate how the interdiffusion problem can be circumvented by using an alternative anode design based on porous and electronically conducting layers......Metal-supported solid oxide fuel cells are expected to offer several potential advantages over conventional anode (Ni-YSZ) supported cells, such as increased resistance against mechanical and thermal stresses and a reduction in materials cost. When Ni-YSZ based anodes are used in metal supported......, into which electrocatalytically active materials are infiltrated after sintering. The paper presents the recent results on the electrochemical performance and durability of the novel planar metal-supported SOFC design. The results presented in the paper show that the novel cell and anode design has...

  9. Energy-savvy solid-state and sonochemical synthesis of lithium sodium titanate as an anode active material for Li-ion batteries

    Science.gov (United States)

    Ghosh, Swatilekha; Kee, Yongho; Okada, Shigeto; Barpanda, Prabeer

    2015-11-01

    Lithium sodium titanate insertion-type anode has been synthesized by classical solid-state (dry) and an alternate solution-assisted (wet) sonochemical synthesis routes. Successful synthesis of the target compound has been realized using simple Na- and Li-hydroxide salts along with titania. In contrast to the previous reports, these energy-savvy synthesis routes can yield the final product by calcination at 650-750 °C for limited duration of 1-10 h. Owing to the restricted calcination duration (dry route for 1-2 h and wet route for 1-5 h), they yield homogeneous nanoscale lithium sodium titanate particles. Sonochemical synthesis reduces the lithium sodium titanate particle size down to 80-100 nm vis-à-vis solid-state method delivering larger (200-500 nm) particles. Independent of the synthetic methods, the end products deliver reversible electrochemical performance with reversible capacity exceeding 80 mAh·g-1 acting as a 1.3 V anode for Li-ion batteries.

  10. Electrochemical properties of ZnO added with Zn-Al-hydrotalcites as anode materials for Zinc/Nickel alkaline secondary batteries

    International Nuclear Information System (INIS)

    Zn-Al layer double hydroxides (LDHs) were prepared through a simple hydrothermal method and proposed as an anode additive for Zn/Ni alkaline secondary batteries. The X-ray diffraction (XRD) and scanning electron microscopy (SEM) of sample LDHs indicates that LDHs was well prepared. The electrochemical properties of the ZnO anodes with different contents of Zn-Al-LDHs were investigated by galvanostatic charge-discharge, cyclic voltammetry (CV) and electrochemical impedance spectroscope (EIS). The structures and morphologies after cycles were also measured by SEM. The results indicate that the presence of Zn-Al-LDHs in the electrode exhibits better electrochemical performance compared with the pure ZnO electrode, such as superior electrochemical cycle stability, better reversibility and higher discharge capacity and utilization ratio. Especially for the electrode added with 24% Zn-Al-LDHs, the discharge capacity hardly declined over 250 cycles, the average utilization ratio could reach 98.5%, and the electrode had no obvious shape change and Zn dendrites after the cycling tests

  11. Highly-Ordered Magnéli Ti4O7 Nanotube Arrays as Effective Anodic Material for Electro-oxidation

    International Nuclear Information System (INIS)

    Pure Magnéli Ti4O7 nanotube arrays (NTA) were successfully fabricated by reducing TiO2 NTA with hydrogen at 850 °C for 30 minutes. The microstructure, composition and electrochemical behavior of the prepared Ti4O7 NTA were characterized by means of X-ray Diffraction, Scanning Electron Microscopy, Transmission Electron Microscopy, X-ray Photoelectron Spectroscopy, Cyclic Voltammetry and Electrochemical Impedance Spectroscopy. The as-prepared Ti4O7 NTA had a highly-ordered tubular structure with high crystallinity, large electrochemical window of water electrolysis (2.4 V vs. Ag/AgCl, pH = 6.0) and low interfacial charge transfer resistance when they were employed as anode for electro-oxidation. Phenol was electro-oxidized on Ti4O7 particles and Ti4O7 NTA with the latter giving 20% more Chemical Oxygen Demand (COD) removal. Pure Ti4O7 NTA also displayed larger degradation coefficient as well as higher COD removal and current efficiency than Boron-doped Diamond and other types of Magnéli NTAs. Cathodic polarization was found to be an effective way of restoring the electrochemical performance of oxidized Ti4O7 NTA as an anode

  12. New development of anodizing process of magnesium alloys

    Institute of Scientific and Technical Information of China (English)

    BAI Li-qun; LI Di

    2004-01-01

    Magnesium alloy, a kind of environment-friendly material with promising and excellent properties, is a good choice for a number of applications. The research and development of anodizing on magnesium alloys and its application situation are reviewed, and the anodizing development trend on magnesium alloys is summarized.

  13. Battery, especially for portable devices, has an anode containing silicon

    NARCIS (Netherlands)

    Kan, S.Y.

    2002-01-01

    The anode (2) contains silicon. A battery with a silicon-containing anode is claimed. An Independent claim is also included for a method used to make the battery, comprising the doping of a silicon substrate (1) with charge capacity-increasing material (preferably boron, phosphorous or arsenic), etc

  14. Disodium terephthalate (Na{sub 2}C{sub 8}H{sub 4}O{sub 4}) as high performance anode material for low-cost room-temperature sodium-ion battery

    Energy Technology Data Exchange (ETDEWEB)

    Zhao, Liang; Hu, Yong-Sheng; Li, Hong; Armand, Michel; Chen, Liquan [Key Laboratory for Renewable Energy, Beijing Key Laboratory for New, Energy Materials and Devices, Beijing National Laboratory for Condensed Matter Physics, Institute of Physics, Chinese Academy of Sciences, Beijing (China); Zhao, Junmei [Key Laboratory of Green Process and Engineering, Institute of Process Engineering, Chinese Academy of Sciences, Beijing (China); Zhou, Zhibin [School of Chemistry and Chemical Engineering, Huazhong University of Science and Technology, Wuhan (China)

    2012-08-15

    In this contribution, a cheap organic material, disodium terephthalate, Na{sub 2}C{sub 8}H{sub 4}O{sub 4}, has been firstly evaluated as a novel anode for room-temperature Na-ion batteries. The material exhibits a high reversible capacity of 250 mAh/g with excellent cycleability. The average Na storage voltage is approximately 0.43 V vs. Na{sup +}/Na. A thin layer of Al{sub 2}O{sub 3} coating on the electrode surface derived from the atomic layer deposition technique is effective in further enhancing Na storage performance. (Copyright copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  15. Low cost fuel cell diffusion layer configured for optimized anode water management

    Science.gov (United States)

    Owejan, Jon P; Nicotera, Paul D; Mench, Matthew M; Evans, Robert E

    2013-08-27

    A fuel cell comprises a cathode gas diffusion layer, a cathode catalyst layer, an anode gas diffusion layer, an anode catalyst layer and an electrolyte. The diffusion resistance of the anode gas diffusion layer when operated with anode fuel is higher than the diffusion resistance of the cathode gas diffusion layer. The anode gas diffusion layer may comprise filler particles having in-plane platelet geometries and be made of lower cost materials and manufacturing processes than currently available commercial carbon fiber substrates. The diffusion resistance difference between the anode gas diffusion layer and the cathode gas diffusion layer may allow for passive water balance control.

  16. Optimal Conditions for Fast Charging and Long Cycling Stability of Silicon Microwire Anodes for Lithium Ion Batteries, and Comparison with the Performance of Other Si Anode Concepts

    Directory of Open Access Journals (Sweden)

    Enrique Quiroga-González

    2013-10-01

    Full Text Available Cycling tests under various conditions have been performed for lithium ion battery anodes made from free-standing silicon microwires embedded at one end in a copper current collector. Optimum charging/discharging conditions have been found for which the anode shows negligible fading (< 0.001% over 80 cycles; an outstanding result for this kind of anodes. Several performance parameters of the anode have been compared to the ones of other Si anode concepts, showing that especially the capacity as well as the rates of charge flow per nominal area of anode are the highest for the present anode. With regard to applications, the specific parameters per area are more important than the specific gravimetric parameters like the gravimetric capacity, which is good for comparing the capacity between materials but not enough for comparing between anodes.

  17. 锂离子电池负极材料Li4Ti5O12的研究概况%Research on Li4Ti5O12anode materials for lithium-ion battery

    Institute of Scientific and Technical Information of China (English)

    樊勇利; 李文升

    2011-01-01

    The research development of anode materials Li4Ti5O12 for Li-ion battery was reviewed in the recent ten years, including structure, synthesis, modification, application. and etc., which was expected to provide some help for commerical applications of LiTiO12 anode, realize some techical breaks, and explore the earlier apolication to power Li-ion battery.%对近10年来锂离子电池负极材料Li4 Ti5 O(12)研究概况如结构、合成方法、改性、应用等方面情况进行综述,以期在Li4Ti5012的商业化应用研究方面提供帮助,实现一些技术突破,为Li4Ti5O12早日应用于动力锂离子电池上做一些探索.

  18. Anodic Stripping Voltammetry: An Instrumental Analysis Experiment.

    Science.gov (United States)

    Wang, Joseph

    1983-01-01

    Describes an experiment designed to acquaint students with the theory and applications of anodic stripping voltammetry (ASV) as well as such ASV problems as contamination associated with trace analysis. The experimental procedure, instrumentation, and materials discussed are designed to minimize cost and keep procedures as simple as possible. (JM)

  19. Study on selenium extraction from anode slime

    Institute of Scientific and Technical Information of China (English)

    2005-01-01

    Taking a copper anode slime as the raw material, a novel process for selenium extraction was studied. The primary selenium recovery can reach above 88.5 % and the quality index of selenium product can be up to 99.5 %. The economic benefit resulted is remarkable and environment has been protected.

  20. Improving Efficiency of Aluminium Sacrificial Anode Using Cold Work Process

    Science.gov (United States)

    Asmara, Y. P.; Siregar, J. P.; Tezara, C.; Ann, Chang Tai

    2016-02-01

    Aluminium is one of the preferred materials to be used as sacrificial anode for carbon steel protection. The efficiency of these can be low due to the formation of oxide layer which passivate the anodes. Currently, to improve its efficiency, there are efforts using a new technique called surface modifications. The objective of this research is to study corrosion mechanism of aluminium sacrificial anode which has been processed by cold work. The cold works are applied by reducing the thickness of aluminium sacrificial anodes at 20% and 40% of thickness reduction. The cathodic protection experiments were performed by immersion of aluminium connected to carbon steel cylinder in 3% NaCl solutions. Visual inspections using SEM had been conducted during the experiments and corrosion rate data were taken in every week for 8 weeks of immersion time. Corrosion rate data were measured using weight loss and linear polarization technique (LPR). From the results, it is observed that cold worked aluminium sacrificial anode have a better corrosion performance. It shows higher corrosion rate and lower corrosion potential. The anodes also provided a long functional for sacrificial anode before it stop working. From SEM investigation, it is shown that cold works have changed the microstructure of anodes which is suspected in increasing corrosion rate and cause de-passivate of the surface anodes.

  1. Anodic dissolution of metals in ionic liquids

    OpenAIRE

    Abbott, Andrew P.; Gero Frisch; Jennifer Hartley; Wrya O. Karim; Ryder, Karl S.

    2015-01-01

    The anodic dissolution of metals is an important topic for battery design, material finishing and metal digestion. Ionic liquids are being used in all of these areas but the research on the anodic dissolution is relatively few in these media. This study investigates the behaviour of 9 metals in an ionic liquid [C4mim][Cl] and a deep eutectic solvent, Ethaline, which is a 1:2 mol ratio mixture of choline chloride and ethylene glycol. It is shown that for the majority of metals studied a quasi-...

  2. A- and B-site doping effect on physicochemical properties of Sr2‑xBaxMMoO6 (M = Mg, Mn, Fe) double perovskites — candidate anode materials for SOFCs

    Science.gov (United States)

    Zheng, Kun; Świerczek, Konrad

    2016-06-01

    In this work, we evaluate the physicochemical properties of Sr2‑xBaxMMoO6 (M = Mg, Mn, Fe) double perovskites as alternative anode materials for solid oxide fuel cells, for which the effect of substitution of strontium by barium in a full range of compositions is studied. The crystal structure, microstructure, characterization of transport properties (electrical conductivity, Seebeck coefficient) and oxygen content as a function of temperature, as well as chemical stability in oxidizing and reducing conditions are discussed. Fe- and Mo-containing Sr2‑xBaxFeMoO6 oxides show very high total conductivities with values of 100-1000 Sṡcm‑1, while Sr2‑xBaxMgMoO6 present good redox stability.

  3. Hydrothermal synthesis of Li4-xNaxTi5O12 and Li4-xNaxTi5O12/graphene composites as anode materials for lithium-ion batteries

    Directory of Open Access Journals (Sweden)

    Zhu Jiping

    2016-01-01

    Full Text Available A potential Lithium-ion battery anode material Li4-xNaxTi5O12 (0≤x≤0.15 has been synthesized via a facile hydrothermal method with short processing time and low temperature. The XRD and FE-SEM results indicate that samples with Na-doped are well-crystallized and have more homogeneous particle distributions with smaller overall particle size in the range of 300-600nm. Electrochemical tests reveal that Na-doped samples exhibit impressive specific capacity and cycle stability compared to pristine Li4Ti5O12 at high rate. The Li3.9Na0.1Ti5O12 electrode deliver an initial specific discharge capacity of 169mAh/g at 0.5C and maintained at 150.4mAh/g even after 40 cycles with the reversible retention of 88.99%. Finally, a simple solvothermal reduction method was used to fabricate Li3.9Na0.1Ti5O12/graphene(Li3.9Na0.1Ti5O12/G composite. Galvanostatic charge-discharge tests demonstrate that this sample has remarkable capacities of 197.4mAh/g and 175.5mAh/g at 0.2C and 0.5C rate, respectively. This indicates that the Li3.9Na0.1Ti5O12/G composite is a promising anode material for using in lithium-ion batteries.

  4. Novel MnOx@Carbon hybrid nanowires with core/shell architecture as highly reversible anode materials for lithium ion batteries

    International Nuclear Information System (INIS)

    Novel MnOx@Carbon hybrid nanowires were successfully synthesized by the combination of a hydrothermal process and a simple PVP (polyvinylpyrrolidone) – solution-soaking method followed by a subsequent carbonization treatment. The nanostructures exhibit the unique feature of having nanocrystalline manganese oxide particle encapsulated inside and an amorphous carbon layer coating the outside. The unique porous characteristics with many meso/micro-pores, and further the highly conductive carbon matrix would lead to the excellent electrochemical performance of the MnOx@Carbon nanowire electrode. The MnOx@Carbon hybrid nanowires exhibit a high initial reversible capacity of 824.4 mAhg−1, a reversible capacity of approximately 541 mAhg−1 after 54 cycles, and excellent cycling stability and rate capability with specific capacity of 298.24 mAhg−1 when cycled at the current density of 1000 mAg−1, which indicates that the composite is a promising anode candidate for Li-ion batteries. - Highlights: • MnOx@C composite were obtained by hydrothermal and PVP-solution-soaking method. • The structures is characteristic of MnOx nanocrystals coated into carbon matrix. • The electrode exhibits good Li+ capacities, cycling stability and rate capability

  5. Scalable synthesis of core-shell structured SiOx/nitrogen-doped carbon composite as a high-performance anode material for lithium-ion batteries

    Science.gov (United States)

    Shi, Lu; Wang, Weikun; Wang, Anbang; Yuan, Keguo; Jin, Zhaoqing; Yang, Yusheng

    2016-06-01

    In this work, a novel core-shell structured SiOx/nitrogen-doped carbon composite has been prepared by simply dispersing the SiOx particles, which are synthesized by a thermal evaporation method from an equimolar mixture of Si and SiO2, into the dopamine solution, followed by a carbonization process. The SiOx core is well covered by the conformal and homogeneous nitrogen-doped carbon layer from the pyrolysis of polydopamine. By contrast with the bare SiOx, the electrochemical performance of the as-prepared core-shell structured SiOx/nitrogen-doped carbon composite has been improved significantly. It delivers a reversible capacity of 1514 mA h g-1 after 100 cycles at a current density of 100 mA g-1 and 933 mA h g-1 at 2 A g-1, much higher than those of commercial graphite anodes. The nitrogen-doped carbon layer ensures the excellent electrochemical performance of the SiOx/C composite. In addition, since dopamine can self-polymerize and coat virtually any surface, this versatile, facile and highly efficient coating process may be widely applicable to obtain various composites with uniform nitrogen-doped carbon coating layer.

  6. Reduced graphene oxide/carbon nanotubes sponge: A new high capacity and long life anode material for sodium-ion batteries

    Science.gov (United States)

    Yan, Dong; Xu, Xingtao; Lu, Ting; Hu, Bingwen; Chua, Daniel H. C.; Pan, Likun

    2016-06-01

    Reduced graphene oxide/carbon nanotubes (CNTs) sponge (GCNTS) is fabricated via a simple freeze drying of graphene oxide/CNTs mixed solution and subsequent thermal treatment in nitrogen atmosphere, and used as anodes for sodium-ion batteries (SIBs) for the first time. The morphology, structure and electrochemical performance of GCNTS are characterized by field emission scanning electron microscopy, transmission electron microscopy, X-ray diffraction, X-ray photoelectron spectroscopy, Raman spectroscopy, nitrogen adsorption-desorption isotherms, galvanostatic charge/discharge tests, cyclic voltammetry and electrochemical impedance spectroscopy, respectively. The results show that GCNTS with 20 wt % CNTs has a highest charge capacity of 436 mA h g-1 after 100 cycles at a current density of 50 mA g-1 and even at a high current density of 10 A g-1, a capacity of 195 mA h g-1 is maintained after 7440 cycles. The high capacity, excellent rate performance and long life cycling enable the GCNTS to be a promising candidate for practical SIBs.

  7. Double anodization experiments in tantalum

    Energy Technology Data Exchange (ETDEWEB)

    Albella, J.M.; Fernandez, M.; Gomez-Aleixandre, C.; Martinez-Duart, J.M.; Montero, I.

    1985-10-01

    Based on our previous model of anodization, a new formula is given for the relation between the breakdown voltage V /SUB B/ during the anodic oxidation of tantalum and the anodization parameters. The formula predicts the well known diminution of V /SUB B/ with the logarithm of the electrolyte concentration. The model also explains the experimentally-observed fact that V /SUB B/ is solely determined by the latter electrolyte in double anodization experiments.

  8. Modified strontium titanates: From defect chemistry to SOFC anodes

    DEFF Research Database (Denmark)

    Verbraeken, M.C.; Ramos, Tania; Agersted, Karsten;

    2015-01-01

    Modified strontium titanates have received much attention recently for their potential as anode material in solid oxide fuel cells (SOFC). Their inherent redox stability and superior tolerance to sulphur poisoning and coking as compared to Ni based cermet anodes could improve durability of SOFC...... systems dramatically. Various substitution strategies can be deployed to optimise materials properties in these strontium titanates, such as electronic conductivity, electrocatalytic activity, chemical stability and sinterability, and thus mechanical strength. Substitution strategies not only cover choice...

  9. Inert Anode Report

    Energy Technology Data Exchange (ETDEWEB)

    none,

    1999-07-01

    This ASME report provides a broad assessment of open literature and patents that exist in the area of inert anodes and their related cathode systems and cell designs, technologies that are relevant for the advanced smelting of aluminum. The report also discusses the opportunities, barriers, and issues associated with these technologies from a technical, environmental, and economic viewpoint.

  10. Molybdenum doped Pr0.5Ba0.5MnO3-δ (Mo-PBMO) double perovskite as a potential solid oxide fuel cell anode material

    Science.gov (United States)

    Sun, Yi-Fei; Zhang, Ya-Qian; Hua, Bin; Behnamian, Yashar; Li, Jian; Cui, Shao-Hua; Li, Jian-Hui; Luo, Jing-Li

    2016-01-01

    A layered Mo doped Pr0.5Ba0.5MnO3-δ (Mo-PBMO) double perovskite oxide was prepared by a modified sol-gel method and the properties of the fabricated material are characterized by various technologies. The results of X-ray diffraction (XRD), H2-temperature programmed reduction (H2-TPR), NH3-temperature programmed desorption (NH3-TPD), and thermogravimetric analysis (TGA) demonstrate that the treatment in reducing atmosphere at high temperature lead to a significant phase transformation of the material to a single cubic phase as well as with the Mo in multiple oxidized states. Such character leads to the production of large amount of oxygen deficiency with facilitated oxygen diffusion. The electrochemical performance tests of half-cell and single cell SOFCs exhibit the promoted effect of Mo on catalytic activity for the oxidation of H2 and CH4, indicating that Mo-PBMO could serve as an anode material candidate for SOFCs.

  11. Research Progress of High Capacity Si Based Anode Material for Li-Ion Battery%锂离子电池用高容量合金类硅基负极材料研究进展

    Institute of Scientific and Technical Information of China (English)

    沈龙; 董爱想; 乔永民; 吴敏昌

    2012-01-01

      锡、硅负极材料由于具有高的比容量等优点,成为提高锂离子电池能量密度的首选负极材料。首先介绍了目前产业界开发锡、硅负极材料的进展,并从商业化的角度比较了这两类材料在开发工艺及实际使用电性能方面的区别。进一步从基础研发角度重点阐述了不同结构的硅基材料(单质硅、硅氧化物、硅碳复合物及硅合金)的电性能改性研究进展,指出了具有工业化前景的工艺方法。%  Tin and Silicon-based compounds are the research focuses of high capacity anode material for lithium ion batteries. The research progress of Si&Sn materials is introduced, and their process development from commercial perspective is also compared. The electrochemical behaviors modification progresses of Si materials, which are crystal silicon、silicon oxygen compound, Si/C composite and silicon alloy, have been reported. The process route which is fit for industrialization has been provided.

  12. Effects of structural patterns and degree of crystallinity on the performance of nanostructured ZnO as anode material for lithium-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Xiao, Liang, E-mail: xiaoliang@whut.edu.cn; Mei, Daidi; Cao, Minglei; Qu, Deyu; Deng, Bohua

    2015-04-05

    Highlights: • Effects of structural patterns on nanostructured ZnO anode are studied. • Structural patterns with sufficient inner spacing show better capacity retention. • Capacity of nanostructured ZnO increase with the increasing of crystallinity. • Crystallized ZnO with inner spacing are expected to have good performance. - Abstract: The effects of structural patterns and degree of crystallinity on the electrochemical performance of ZnO were systematically studied using a controllable synthesis. The microspheres assembled with distorted nanosheets, hexagonal nanorods and radial assembly of nanorods of ZnO were successfully prepared by the hydrothermal reaction of zinc nitrate, hexamethylenetetramine and different amount of trisodium citrate. ZnO microspheres were calcinated at different temperatures (300, 600 and 900 °C) to increase their degree of crystallization. Constant current charge and discharge measurements show that the capacity retention of the microspheres and radial assembled nanorods are higher than that of hexagonal nanorods. This may be due to their inner spacing of specific structure patterns that can accommodate and restrain the volume changes during cycling. Additionally, the capacity of ZnO microspheres can be improved by short-time calcinations at 600 or 900 °C for their crystallization. The studies of differential capacity versus potential plots indicate that the enhanced degree of crystallization facilitates the alloying and dealloying of the reduction products of ZnO. Therefore, both large specific capacity and good capacity retention can be expected with highly crystallized specific nanostructures of ZnO with the sufficient inner spacing. The ZnO microspheres calcinated at 600 °C show the best performance with a specific capacity of 1328.2 mA h g{sup −1} for the first cycle and 662.8 mA h g{sup −1} for the 50th cycle at 0.1 C with an operating potential of 0.05–3.00 V.

  13. Facile synthesis of MgCo{sub 2}O{sub 4} nanowires as binder-free flexible anode materials for high-performance Li-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Xiujuan; Zhai, Gaohong, E-mail: zgh@nwu.edu.cn; Wang, Hui, E-mail: hwangnwu@sina.cn, E-mail: huiwang@nwu.edu.cn [Northwest University, Key Laboratory of Synthetic and Natural Functional Molecule Chemistry (Ministry of Education), College of Chemistry & Materials Science (China)

    2015-08-15

    MgCo{sub 2}O{sub 4} nanowires are synthesized for the first time through two-step synthesis method, followed by annealing of the MgCo{sub 2}O{sub 4} precursors. The microstructure and morphology of MgCo{sub 2}O{sub 4} nanowires are examined by powder X-ray diffraction, scanning electron microscopy, high-resolution transmission electron microscopy, and X-ray photoelectron spectroscopy. MgCo{sub 2}O{sub 4} nanowires give rise to a BET surface area of 45.1 m{sup 2} g{sup −1} and the adsorption average pore size of 11.5 nm. When tested as an anode for lithium-ion batteries, the MgCo{sub 2}O{sub 4} nanowires electrode exhibit exceptional properties in terms of specific capacity, cycling performance, and rate capacity compared with previously reported Co-based binary metal oxides. For instance, when the current densities increase from 5, 10, 15, and 20 A g{sup −1}, the discharge capacities of the MgCo{sub 2}O{sub 4} nanowires electrode are about 649, 348, 188, and 121 mAh g{sup −1}, respectively. The enhanced electrochemical performance of the MgCo{sub 2}O{sub 4} nanowires can be mainly attributed to the nanostructures which lead to decreased lithium-ion diffusion distances and increased active sites for Li insertion/extraction reactions.

  14. Fundamental Investigation of Silicon Anode in Lithium-Ion Cells

    Science.gov (United States)

    Wu, James J.; Bennett, William R.

    2012-01-01

    Silicon is a promising and attractive anode material to replace graphite for high capacity lithium ion cells since its theoretical capacity is 10 times of graphite and it is an abundant element on Earth. However, there are challenges associated with using silicon as Li-ion anode due to the significant first cycle irreversible capacity loss and subsequent rapid capacity fade during cycling. Understanding solid electrolyte interphase (SEI) formation along with the lithium ion insertion/de-insertion kinetics in silicon anodes will provide greater insight into overcoming these issues, thereby lead to better cycle performance. In this paper, cyclic voltammetry and electrochemical impedance spectroscopy are used to build a fundamental understanding of silicon anodes. The results show that it is difficult to form the SEI film on the surface of a Si anode during the first cycle; the lithium ion insertion and de-insertion kinetics for Si are sluggish, and the cell internal resistance changes with the state of lithiation after electrochemical cycling. These results are compared with those for extensively studied graphite anodes. The understanding gained from this study will help to design better Si anodes, and the combination of cyclic voltammetry with impedance spectroscopy provides a useful tool to evaluate the effectiveness of the design modifications on the Si anode performance.

  15. Efficient and stable iron based perovskite La0.9Ca0.1Fe0.9Nb0.1O3-δ anode material for solid oxide fuel cells

    Science.gov (United States)

    Kong, Xiaowei; Zhou, Xiaoliang; Tian, Yu; Wu, Xiaoyan; Zhang, Jun; Zuo, Wei; Gong, Xiaobo; Guo, Zhanhu

    2016-06-01

    A novel La0.9Ca0.1Fe0.9Nb0.1O3-δ (LCFNb) perovskite for solid oxide fuel cells (SOFCs) anode is prepared by means of the citrate-nitrate route and composited with Ce0.8Sm0.2O1.9 (SDC) by impregnation method to form nano-scaled LCFNb/SDC anode catalytic layers. The single cells with LCFNb and LCFNb/SDC impregnated anodes both achieve relatively high power output with maximum power densities (MPDs) reaching up to 610, 823 mW·cm-2 in H2 at 800 °C, respectively, presenting a high potential of LCFNb for use as SOFCs anode. The power outputs of the single cells with LCFNb/SDC composite anode in CO and syngas (COsbnd H2 mixture) are almost identical to that in H2 at each testing temperature. This composite anode also presents excellent durability in both H2 and CO for as long as 50 h, showing desirable anti-reduction and carbon deposition resistance abilities. Besides, the cell output is stable in 100 ppm H2Ssbnd H2 atmospheres for 20 h at a current density of 600 mA·cm-2 with negligible sulfur accumulation on the anode surface. Hence, a novel iron based perovskite LCFNb anode with remarkable cell performance, carbon deposition resistance and sulfur poisoning tolerance for SOFCs is successfully obtained.

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

    International Nuclear Information System (INIS)

    Highlights: • The nanocarbon anodes in lithium-ion batteries deliver a high capacity of ∼1100 mA h g−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−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−1 at 0.1 A g−1 for MPG, CTN, and HCB, respectively. The capacity of 181, 141, and 139 mA h g−1 at 4 A g−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. Interconnected hollow carbon nanospheres for stable lithium metal anodes.

    Science.gov (United States)

    Zheng, Guangyuan; Lee, Seok Woo; Liang, Zheng; Lee, Hyun-Wook; Yan, Kai; Yao, Hongbin; Wang, Haotian; Li, Weiyang; Chu, Steven; Cui, Yi

    2014-08-01

    For future applications in portable electronics, electric vehicles and grid storage, batteries with higher energy storage density than existing lithium ion batteries need to be developed. Recent efforts in this direction have focused on high-capacity electrode materials such as lithium metal, silicon and tin as anodes, and sulphur and oxygen as cathodes. Lithium metal would be the optimal choice as an anode material, because it has the highest specific capacity (3,860 mAh g(-1)) and the lowest anode potential of all. However, the lithium anode forms dendritic and mossy metal deposits, leading to serious safety concerns and low Coulombic efficiency during charge/discharge cycles. Although advanced characterization techniques have helped shed light on the lithium growth process, effective strategies to improve lithium metal anode cycling remain elusive. Here, we show that coating the lithium metal anode with a monolayer of interconnected amorphous hollow carbon nanospheres helps isolate the lithium metal depositions and facilitates the formation of a stable solid electrolyte interphase. We show that lithium dendrites do not form up to a practical current density of 1 mA cm(-2). The Coulombic efficiency improves to ∼ 99% for more than 150 cycles. This is significantly better than the bare unmodified samples, which usually show rapid Coulombic efficiency decay in fewer than 100 cycles. Our results indicate that nanoscale interfacial engineering could be a promising strategy to tackle the intrinsic problems of lithium metal anodes. PMID:25064396

  18. The effect of antimony presence in anodic copper on kinetics and mechanism of anodic dissolution and cathodic deposition of copper

    Directory of Open Access Journals (Sweden)

    Stanković Z.D.

    2008-01-01

    Full Text Available The influence of the presence of Sb atoms, as foreign metal atoms in anode copper, on kinetics, and, on the mechanism of anodic dissolution and cathodic deposition of copper in acidic sulfate solution has been investigated. The galvanostatic single-pulse method has been used. Results indicate that presence of Sb atoms in anode copper increase the exchange current density as determined from the Tafel analysis of the electrode reaction. It is attributed to the increase of the crystal lattice parameter determined from XRD analysis of the electrode material.

  19. Metal-Supported SOFC with Ceramic-Based Anode

    DEFF Research Database (Denmark)

    Blennow Tullmar, Peter; Klemensø, Trine; Persson, Åsa Helen;

    2011-01-01

    Metal-supported solid oxide fuel cells have shown promise to offer several potential advantages over conventional anode (Ni-YSZ) supported cells, such as increased resistance against mechanical and thermal stresses and a reduction in materials cost. The purpose of this work is to illustrate how......), zirconia-free anode, in a planar metal-supported SOFC concept is discussed. ©2011 COPYRIGHT ECS - The Electrochemical Society...

  20. Photoelectrochemical cell with nondissolving anode

    Science.gov (United States)

    Ellis, A. B.; Kaiser, S. W.; Wrighton, M. S.

    1980-01-01

    Improved electrolytic cells have efficiencies comparable to those of best silicon solar cells but are potentially less expensive to manufacture. Cells consist of light-sensitive n-type semiconductor anode and metallic cathode immersed in electrolytic solution. Reversible redox cells produce no chemical change in electrolyte and stabilize anode against dissolving. Cell can produce more than 500 mW of power per square centimeter of anode area at output voltage of 0.4 V.

  1. 锰氧化物/石墨烯复合材料作为锂离子电池负极的研究%A study on MnO_x/graphene composites as anode materials for lithium ion batteries

    Institute of Scientific and Technical Information of China (English)

    高云雷; 赵东林; 沈曾民

    2012-01-01

    The precursor of Mn hybrid material was synthesized by a modified Hummers method and MnOx/graphene composites were obtained through a reduction in nitrogen and hydrogen atmosphere at 400℃.The composite material was investigated as anode materials for lithium ion batteries via scanning and transmission electron microscopy(TEM),X-ray diffraction(XRD) and a variety of electrochemical testing techniques.Experimental results showed that nano-particles of manganese oxide were well dispersed on the surface of graphene sheets.The first reversible capacity of the prepared composite was as high as 876mAh/g at current density of 50mA/g.After 30 cycles,the reversible specific capacity was still maintain at more than 700mAh/g.%以天然石墨为原料,采用改进的Hummers法合成含Mn的氧化石墨;400℃条件下氢气还原制备了锰氧化物/石墨烯复合材料。利用XRD、SEM和TEM对所制备的复合材料进行了表征。结果表明锰氧化物(MnOx)颗粒均匀地分布在石墨烯片层表面。将复合材料作为锂离子电池负极进行研究,在50mA/g电流密度下,首次库伦效率为70.4%,可逆容量达876mAh/g,并且具有良好的循环性能,在30次循环后仍保持在700mAh/g以上。

  2. 高性能锂离子电池SiO/C复合负极材料研究%High-performance SiO/C Composite Anode Material for Lithium Ion Battery

    Institute of Scientific and Technical Information of China (English)

    余德馨; 杨学林; 石长川; 张鹏昌

    2011-01-01

    以SiO为硅源,柠檬酸为碳源,通过高能球磨和高温热解制备了一种循环性能优异的锂离子电池SiO/C复合负极材料.采用X-射线衍射仪(XRD)、扫描电子显微镜(SEM)对复合材料的物相和形貌进行了表征.具有孔状结构的柠檬酸热解碳对纳米SiO不仅具有良好的包覆效果,也能有效缓冲电化学嵌脱锂过程中硅颗粒释放出来的体积变化.电化学性能测试表明,SiO/C复合负极材料电极循环100次后容量仍高达803.1 mA·h/g,容量保持率为89%.%SiO/C composite anode material with high capacity, high cycling stability for lithium ion battery is synthesized by high-energy mechanical milling and subsequent heat treatment using silicon-monoxide and citric acid as raw materials. The phase composition and micro morphology of the composite material are investigated by the X-ray diffractometer(XRD) and scanning electron microscope(SEM), indicating nano-sized SiO particles was coated by pyrolytic carbon with porous feature. SiO/C composite electrode presents excellent electrochemical performance with reversible capacity as high as 803.1 mA·h/g and capacity retention rate of 89% after 100 cycles.

  3. The effect of grain size on aluminum anodes for Al-air batteries in alkaline electrolytes

    Science.gov (United States)

    Fan, Liang; Lu, Huimin

    2015-06-01

    Aluminum is an ideal material for metallic fuel cells. In this research, different grain sizes of aluminum anodes are prepared by equal channel angular pressing (ECAP) at room temperature. Microstructure of the anodes is examined by electron backscatter diffraction (EBSD) in scanning electron microscope (SEM). Hydrogen corrosion rates of the Al anodes in 4 mol L-1 NaOH are determined by hydrogen collection method. The electrochemical properties of the aluminum anodes are investigated in the same electrolyte using electrochemical impedance spectroscopy (EIS) and polarization curves. Battery performance is also tested by constant current discharge at different current densities. Results confirm that the electrochemical properties of the aluminum anodes are related to grain size. Finer grain size anode restrains hydrogen evolution, improves electrochemical activity and increases anodic utilization rate. The proposed method is shown to effectively improve the performance of Al-air batteries.

  4. Structural stabilities, surface morphologies and electronic properties of spinel LiTi2O4 as anode materials for lithium-ion battery: A first-principles investigation

    Science.gov (United States)

    Wang, Qi; Yu, Hai-Tao; Xie, Ying; Li, Ming-Xia; Yi, Ting-Feng; Guo, Chen-Feng; Song, Qing-Shan; Lou, Ming; Fan, Shan-Shan

    2016-07-01

    The thermodynamic stabilities, surface morphologies, and electronic structures of the LiTi2O4 compound were investigated by the first-principles methods. The formation enthalpies and lattice constants of LixTi2O4 decrease at first and then increase again. This phenomenon is related to the balance between Lisbnd O attractions and Lisbnd Li repulsions. Population analysis revealed that pure ionic and strong covalent bonds are formed respectively between lithium and oxygen and between titanium and oxygen in LiTi2O4 material. These interactions are very crucial for the thermodynamic stability of the compounds. The surface stability was considered as functions of the chemical potentials, and five terminations, (100)-Ti2O4, (110)-Ti2O4, (210)-Ti2O4, (111)-LiTiO4, and (310)-Ti2O8ones, are dominant in the stability diagram. Our calculation showed that a particle morphology with mono (110) facet can be obtained at Ti- and/or O-moderate conditions, and this morphology will be very helpful for improving the rate performance of the material via reduction of the lithium diffusion distance. Furthermore, partially filled electronic states at the Fermi energy were confirmed for bulk LiTi2O4 and some of the surfaces, and they are responsible for the excellent electronic conductivity of the material. Further calculations showed that the work functions are sensitive to the stoichiometry of the surfaces.

  5. Investigation of mechanism of anode plasma formation in ion diode with dielectric anode

    Science.gov (United States)

    Pushkarev, A.

    2015-10-01

    The results of investigation of the anode plasma formation in a diode with a passive anode in magnetic insulation mode are presented. The experiments have been conducted using the BIPPAB-450 ion accelerator (350-400 kV, 6-8 kA, 80 ns) with a focusing conical diode with Br external magnetic field (a barrel diode). For analysis of plasma formation at the anode and the distribution of the ions beam energy density, infrared imaging diagnostics (spatial resolution of 1-2 mm) is used. For analysis of the ion beam composition, time-of-flight diagnostics (temporal resolution of 1 ns) were used. Our studies have shown that when the magnetic induction in the A-C gap is much larger than the critical value, the ion beam energy density is close to the one-dimensional Child-Langmuir limit on the entire working surface of the diode. Formation of anode plasma takes place only by the flashover of the dielectric anode surface. In this mode, the ion beam consists primarily of singly ionized carbon ions, and the delay of the start of formation of the anode plasma is 10-15 ns. By reducing the magnetic induction in the A-C gap to a value close to the critical one, the ion beam energy density is 3-6 times higher than that calculated by the one-dimensional Child-Langmuir limit, but the energy density of the ion beam is non-uniform in cross-section. In this mode, the anode plasma formation occurs due to ionization of the anode material with accelerated electrons. In this mode, also, the delay in the start of the formation of the anode plasma is much smaller and the degree of ionization of carbon ions is higher. In all modes occurred effective suppression of the electronic component of the total current, and the diode impedance was 20-30 times higher than the values calculated for the mode without magnetic insulation of the electrons. The divergence of the ion beam was 4.5°-6°.

  6. Studies of a liquid anode for plutonium electrorefining

    International Nuclear Information System (INIS)

    They are developing a solvent anode as an alternate method for producing plutonium metal of high purity by an electrorefining process. The goals are to produce metal of 99.98% purity with an anode residue containing less than 2% of the plutonium in the feed material. If they are successful, they will design and demonstrate a system utilizing semi-continuous and remotely controlled operations. Establishing a solvent anode method should lead to improved yields and a substantial reduction in the amount of residues generated by the electrorefining process. The new method should be a viable pyrochemical technique for recovering both plutonium and uranium from spent reactor fuel. Initially, the anode consists of a tantalum rod immersed in a pool of liquid cadmium at 7400C. Impure plutonium or a solid anode residue is in contact with the cadmium. As current passes through the anode, plutonium in the cadmium is oxidized and transfers into the molten salt as tripositive plutonium. More plutonium dissolves into the cadmium and the oxidation continues. The tri-positive plutonium is carried through the salt to the cathode, where it is reduced to pure, liquid metal. This metal, which is heavier than the salt, drips from the cathode into an annulus between the anode and cathode compartments and forms a product ring

  7. Atmospheric pressure arc discharge with ablating graphite anode

    Energy Technology Data Exchange (ETDEWEB)

    Nemchinsky, V. A. [Keiser University, Fort Lauderdale Campus, FL, 33309, USA; Raitses, Y. [Princeton Plasma Physics Lab. (PPPL), Princeton, NJ (United States)

    2015-05-18

    The anodic carbon arc discharge is used to produce carbon nanoparticles. Recent experiments with the carbon arc at atmospheric pressure helium demonstrated the enhanced ablation rate for narrow graphite anodes resulting in high deposition rates of carbonaceous products on the copper cathode (Fetterman et al 2008 Carbon 46 1322–6). The proposed model explains these results with interconnected steady-state models of the cathode and the anode processes. When considering cathode functioning, the model predicts circulation of the particles in the near-cathode region: evaporation of the cathode material, ionization of evaporated atoms and molecules in the near-cathode plasma, return of the resulting ions to the cathode, surface recombination of ions and electrons followed again by cathode evaporation etc. In the case of the low anode ablation rate, the ion acceleration in the cathode sheath provides the major cathode heating mechanism. In the case of an intensive anode ablation, an additional cathode heating is due to latent fusion heat of the atomic species evaporated from the anode and depositing at the cathode. Using the experimental arc voltage as the only input discharge parameter, the model allows us to calculate the anode ablation rate. A comparison of the results of calculations with the available experimental data shows reasonable agreement.

  8. In situ characterization of nanoscale catalysts during anodic redox processes

    Energy Technology Data Exchange (ETDEWEB)

    Sharma, Renu [National Institute of Standards and Technology; Crozier, Peter [Arizona State University; Adams, James [Arizona State University

    2013-09-19

    Controlling the structure and composition of the anode is critical to achieving high efficiency and good long-term performance. In addition to being a mixed electronic and ionic conductor, the ideal anode material should act as an efficient catalyst for oxidizing hydrogen, carbon monoxide and dry hydrocarbons without de-activating through either sintering or coking. It is also important to develop novel anode materials that can operate at lower temperatures to reduce costs and minimized materials failure associated with high temperature cycling. We proposed to synthesize and characterize novel anode cermets materials based on ceria doped with Pr and/or Gd together with either a Ni or Cu metallic components. Ceria is a good oxidation catalyst and is an ionic conductor at room temperature. Doping it with trivalent rare earths such as Pr or Gd retards sintering and makes it a mixed ion conductor (ionic and electronic). We have developed a fundamental scientific understanding of the behavior of the cermet material under reaction conditions by following the catalytic oxidation process at the atomic scale using a powerful Environmental Scanning Transmission Electron Microscope (ESTEM). The ESTEM allowed in situ monitoring of structural, chemical and morphological changes occurring at the cermet under conditions approximating that of typical fuel-cell operation. Density functional calculations were employed to determine the underlying mechanisms and reaction pathways during anode oxidation reactions. The dynamic behavior of nanoscale catalytic oxidation of hydrogen and methane were used to determine: ? Fundamental processes during anodic reactions in hydrogen and carbonaceous atmospheres ? Interfacial effects between metal particles and doped ceria ? Kinetics of redox reaction in the anode material

  9. High performance anode for advanced Li batteries

    Energy Technology Data Exchange (ETDEWEB)

    Lake, Carla [Applied Sciences, Inc., Cedarville, OH (United States)

    2015-11-02

    The overall objective of this Phase I SBIR effort was to advance the manufacturing technology for ASI’s Si-CNF high-performance anode by creating a framework for large volume production and utilization of low-cost Si-coated carbon nanofibers (Si-CNF) for the battery industry. This project explores the use of nano-structured silicon which is deposited on a nano-scale carbon filament to achieve the benefits of high cycle life and high charge capacity without the consequent fading of, or failure in the capacity resulting from stress-induced fracturing of the Si particles and de-coupling from the electrode. ASI’s patented coating process distinguishes itself from others, in that it is highly reproducible, readily scalable and results in a Si-CNF composite structure containing 25-30% silicon, with a compositionally graded interface at the Si-CNF interface that significantly improve cycling stability and enhances adhesion of silicon to the carbon fiber support. In Phase I, the team demonstrated the production of the Si-CNF anode material can successfully be transitioned from a static bench-scale reactor into a fluidized bed reactor. In addition, ASI made significant progress in the development of low cost, quick testing methods which can be performed on silicon coated CNFs as a means of quality control. To date, weight change, density, and cycling performance were the key metrics used to validate the high performance anode material. Under this effort, ASI made strides to establish a quality control protocol for the large volume production of Si-CNFs and has identified several key technical thrusts for future work. Using the results of this Phase I effort as a foundation, ASI has defined a path forward to commercialize and deliver high volume and low-cost production of SI-CNF material for anodes in Li-ion batteries.

  10. Graphene-encapsulated Li2MnTi3O8 nanoparticles as a high rate anode material for lithium-ion batteries

    International Nuclear Information System (INIS)

    Highlights: • The new titanate graphene-encapsulated Li2MnTi3O8 is prepared by a one step sol-gel method. • Both of Li2MnTi3O8 and graphene-encapsulated Li2MnTi3O8 show an excellent cycling stability. • Graphene-encapsulation obviously improve the rate capability of Li2MnTi3O8. - Abstract: Graphene-encapsulated Li2MnTi3O8 nanoparticles were synthesized via a modified sol-gel process using graphene oxide as the template. The prepared Li2MnTi3O8 material has a complex spinel structure in the P4332 space group. The morphology of the graphene-encapsulated Li2MnTi3O8 composite indicates that the Li2MnTi3O8 particles can be uniformly scattered on a graphene substrate, and these particles have a size of 10–20 nm. The electrochemical properties indicate that the graphene-encapsulated Li2MnTi3O8 material possesses a stable reversible discharge capacity of ∼220 mAh g-1 after 50 cycles at 0.1 C. In addition, the reversible capacity at 2 C improved by 70% after graphene-encapsulation, which indicates the excellent high rate capability

  11. Corrosion of cermet anodes during low temperature electrolysis of alumina. Final report

    Energy Technology Data Exchange (ETDEWEB)

    Kozarek, R.L.; Ray, S.P.; Dawless, R.K.; LaCamera, A.F.

    1997-09-26

    Successful development of inert anodes to replace carbon anodes in Hall cells has the potential benefits of lower energy consumption,lower operating costs, and reduced CO{sub 2} and CO emissions. Using inert anodes at reduced current density and reduced operating temperature (800 C) has potential for decreasing the corrosion rate of inert anodes. It may also permit the use of new materials for containment and insulation. This report describes the fabrication characteristics and the corrosion performance of 5324-17% Cu Cermet anodes in 100 hour tests. Although some good results were achieved, the corrosion rate at low temperature (800 C) is varied and not significantly lower than typical results at high temperature ({approximately} 960 C). This report also describes several attempts at 200 hour tests, with one anode achieving 177 hours of continuous operation and another achieving a total of 235 hours but requiring three separate tests of the same anode. The longest run did show a lower wear rate in the last test; but a high resistance layer developed on the anode surface and forced an unacceptably low current density. It is recommended that intermediate temperatures be explored as a more optimal environment for inert anodes. Other electrolyte chemistries and anode compositions (especially high conductivity anodes) should be considered to alleviate problems associated with lower temperature operation.

  12. Synthesis and electrochemical performance of hole-rich Li4Ti5O12 anode material for lithium-ion secondary batteries

    Science.gov (United States)

    Zhu, Weibo; Zhuang, Zhenyuan; Yang, Yanmin; Zhang, Ruidan; Lin, Zhiya; Lin, Yingbin; Huang, Zhigao

    2016-06-01

    Hole-rich Li4Ti5O12 composites are synthesized by spray drying using carbon nanotubes as additives in precursor solution, subsequently followed calcinated at high temperature in air. The structure, morphology, and texture of the as-prepared composites are characterized with XRD, Raman, BET and SEM techniques. The electrochemical properties of the as-prepared composites are investigated systematically by charge/discharge testing, cyclic voltammograms and AC impedance spectroscopy, respectively. In comparison with the pristine Li4Ti5O12, the hole-rich Li4Ti5O12 induced by carbon nanotubes exhibits superior electrochemical performance, especially at high rates. The obtained excellent electrochemical performances of should be attributed to the hole-rich structure of the materials, which offers more connection-area with the electrolyte, shorter diffusion-path length as well faster migration rate for both Li ions and electrons during the charge/discharge process.

  13. Nanostructured TiO2:Application as Anode Material of Lithium-Ion Batteries%纳米结构 TiO2作为锂离子电池负极材料的应用

    Institute of Scientific and Technical Information of China (English)

    高琼

    2015-01-01

    TiO2作为新兴的锂离子电池负极活性材料受到广大关注,纳米结构TiO 2由于其独特的结构和性质,电学性能显著提高。本文简要介绍了锐钛矿型TiO 2、金红石型TiO 2、板钛矿型TiO 2和TiO 2-B作为电池负极材料的研究进展,比较了不同晶型之间的结构差异以及脱嵌锂机理,探究了TiO 2倍率性能和循环性能不佳的原因,并提出的可能的解决方案在于TiO 2的小尺寸化和结构功能化。%Extensive attention has been paid to the potential of TiO 2 to act as the negative electrode material for lithium batteries.The electrochemical lithium-storage ability of nanostructured TiO 2 improves obviously due to its wealth of important physical and chemical performances.The research progress in anatase TiO 2 , rutile TiO2 , brookite TiO2 and TiO2 [ B ] used as anode material for lithium batteries was reviewed . The features and lithium insertion/extraction mechanisms of different crystalline were compared . The reasons caused the non -ideal rate capability and cycle performance was discussed and the possible solutions were nanosized and peculiar structure .

  14. Screened Anode N2 Laser

    OpenAIRE

    Sabry, M. Montaser Foad

    1985-01-01

    An experimental study of the effect of screening the discharge channel on the output energy is presented. It has been found that a screened anode nitrogen laser generates higher output energy than that of a screened cathode, and also higher than that when both cathode and anode are unshielded at higher pressures.

  15. Composite anodes for lithium-ion batteries: status and trends

    Directory of Open Access Journals (Sweden)

    Alain Mauger

    2016-07-01

    Full Text Available Presently, the negative electrodes of lithium-ion batteries (LIBs is constituted by carbon-based materials that exhibit a limited specific capacity 372 mAh g−1 associated with the cycle between C and LiC6. Therefore, many efforts are currently made towards the technological development nanostructured materials in which the electrochemical processes occurs as intercalation, alloying or conversion reactions with a good accommodation of dilatation/contraction during cycling. In this review, attention is focused on advanced anode composite materials based on carbon, silicon, germanium, tin, titanium and conversion anode composite based on transition-metal oxides.

  16. Blue fluorescent organic light emitting diodes with multilayered graphene anode

    International Nuclear Information System (INIS)

    As an innovative anode for organic light emitting devices (OLEDs), we have investigated graphene films. Graphene has importance due to its huge potential in flexible OLED applications. In this work, graphene films have been catalytically grown and transferred to the glass substrate for OLED fabrications. We have successfully fabricated 2 mm × 2 mm device area blue fluorescent OLEDs with graphene anodes which showed 2.1% of external quantum efficiency at 1000 cd/m2. This is the highest value reported among fluorescent OLEDs using graphene anodes. Oxygen plasma treatment on graphene has been found to improve hole injections in low voltage regime, which has been interpreted as oxygen plasma induced work function modification. However, plasma treatment also increases the sheet resistance of graphene, limiting the maximum luminance. In summary, our works demonstrate the practical possibility of graphene as an anode material for OLEDs and suggest a processing route which can be applied to various graphene related devices.

  17. Copper anode corrosion affects power generation in microbial fuel cells

    KAUST Repository

    Zhu, Xiuping

    2013-07-16

    Non-corrosive, carbon-based materials are usually used as anodes in microbial fuel cells (MFCs). In some cases, however, metals have been used that can corrode (e.g. copper) or that are corrosion resistant (e.g. stainless steel, SS). Corrosion could increase current through galvanic (abiotic) current production or by increasing exposed surface area, or decrease current due to generation of toxic products from corrosion. In order to directly examine the effects of using corrodible metal anodes, MFCs with Cu were compared with reactors using SS and carbon cloth anodes. MFCs with Cu anodes initially showed high current generation similar to abiotic controls, but subsequently they produced little power (2 mW m-2). Higher power was produced with microbes using SS (12 mW m-2) or carbon cloth (880 mW m-2) anodes, with no power generated by abiotic controls. These results demonstrate that copper is an unsuitable anode material, due to corrosion and likely copper toxicity to microorganisms. © 2013 Society of Chemical Industry.

  18. Superior electrochemical performance of mesoporous Fe{sub 3}O{sub 4}/CNT nanocomposites as anode material for lithium ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Abbas, Syed Mustansar, E-mail: qau_abbas@yahoo.com [Nanoscience and Catalysis Division, National Centre for Physics, Islamabad (Pakistan); Department of Chemistry, Quaid-e-Azam University, Islamabad (Pakistan); Ali, Saqib, E-mail: drsa54@yahoo.com [Department of Chemistry, Quaid-e-Azam University, Islamabad (Pakistan); Niaz, Niaz Ahmad [Department of Physics, Bahauddin Zakariya University, Multan (Pakistan); Ali, Nisar; Ahmed, Rashid [Department of Physics, Faculty of Science, University Teknologi Malaysia, Skudai, Johor (Malaysia); Ahmad, Nisar [Nanoscience and Catalysis Division, National Centre for Physics, Islamabad (Pakistan)

    2014-10-25

    Graphical abstract: The mesoporous Fe{sub 3}O{sub 4}/CNT nanocomposite synthesized via a modified co-precipitation method in combination with subsequent calcination was applied in the negative electrode materials for lithium ion batteries and exhibited high electrochemical performance. - Highlights: • Nanocomposite of functionalized CNTs with Fe{sub 3}O{sub 4} nanoparticles is prepared. • Good quality interfacial adhesion between CNTs and Fe{sub 3}O{sub 4} matrix. • High discharge capacity of 1093 mA h g{sup −1} after 50 cycles. • 50th Cycle coulombic efficiency of 98.4% at a current density of 100 mA g{sup −1}. - Abstract: A series of Fe{sub 3}O{sub 4}/CNT nanocomposites are effectively synthesized by an in situ chemical co-precipitation technique. The structure, morphology and chemical composition of synthesized nanocomposites are analyzed by X-ray diffraction, Rutherford backscattering spectroscopy, scanning electron microscopy, transmission electron microscopy and fourier-transform infrared spectroscopy. The electrochemical performance of synthesized nanocomposites is tested by cyclic voltammetry (CV), charge/discharge studies and electrochemical impedance spectroscopy (EIS). The carbon nanotubes are nicely dispersed in the Fe{sub 3}O{sub 4} nanoparticles for all the nanocomposites. Due to the synergistic effect arising from Fe{sub 3}O{sub 4} nanoparticles and carbon nanotubes, the electrochemical properties of pure Fe{sub 3}O{sub 4} material is considerably enhanced. A discharge capacity of 1093 mA h g{sup −1} is demonstrated by Fe{sub 3}O{sub 4}–7%CNT nanocomposite at a current density of 100 mA g{sup −1} with a high columbic efficiency of 98.4%. Moreover, this nanocomposite shows a stable cycling and rate performance at higher current densities. Hence, based on the above studies, such Fe{sub 3}O{sub 4}/CNT nanocomposite could be a possible contributor for lithium ion batteries.

  19. Elaboration, physical and electrochemical characterizations of CO tolerant PEMFC anode materials. Study of platinum-molybdenum and platinum-tungsten alloys and composites; Elaborations et caracterisations electrochimiques et physiques de materiaux d'anode de PEMFC peu sensibles a l'empoisonnement par CO: etude d'alliages et de composites a base de platine-molybdene et de platine-tungstene

    Energy Technology Data Exchange (ETDEWEB)

    Peyrelade, E.

    2005-06-15

    PEMFC development is hindered by the CO poisoning ability of the anode platinum catalyst. It has been previously shown that the oxidation potential of carbon monoxide adsorbed on the platinum atoms can be lowered using specific Pt based catalysts, either metallic alloys or composites. The objective is then to realize a catalyst for which the CO oxidation is compatible with the working potential of a PEMFC anode. In our approach, to enhance the CO tolerance of platinum based catalyst supported on carbon, we studied platinum-tungsten and platinum-molybdenum alloys and platinum-metal oxide materials (Pt-WO{sub x} and Pt-MoO{sub x}). The platinum based alloys demonstrate a small effect of the second metal towards the oxidation of carbon monoxide. The platinum composites show a better tolerance to carbon monoxide. Electrochemical studies on both Pt-MoO{sub x} and Pt-WO{sub x} demonstrate the ability of the metal-oxides to promote the ability of Pt to oxidize CO at low potentials. However, chrono-amperometric tests reveal a bigger influence of the tungsten oxide. Complex chemistry reactions on the molybdenum oxide surface make it more difficult to observe. (author)

  20. Improving battery safety by reducing the formation of Li dendrites with the use of amorphous silicon polymer anodes

    OpenAIRE

    Hitoshi Maruyama; Hideyuki Nakano; Masahiro Ogawa; Masaaki Nakamoto; Toshiaki Ohta; Akira Sekiguchi

    2015-01-01

    To provide safe lithium-ion batteries (LIBs) at low cost, battery materials which lead to reduced Li dendrite formation are needed. The currently used anode materials have low redox voltages that are very close to the redox potential for the formation of Li metal, which leads to severe short circuiting. Herein, we report that when the three-dimensional amorphous silicon polymers poly(methylsilyne) and poly(phenylsilyne) are used as anode materials, dendritic Li formation on the anode surface ...

  1. Aerogel and xerogel composites for use as carbon anodes

    Science.gov (United States)

    Cooper, John F.; Tillotson, Thomas M.; Hrubesh, Lawrence W.

    2008-08-12

    Disclosed herein are aerogel and xerogel composite materials suitable for use as anodes in fuel cells and batteries. Precursors to the aerogel and xerogel compounds are infused with inorganic polymeric materials or carbon particles and then gelled. The gels are then pyrolyzed to form composites with internal structural support.

  2. Alternative Anodes for the Electrolytic Reduction of Uranium Dioxide

    Science.gov (United States)

    Merwin, Augustus

    Reprocessing of spent nuclear fuel is an essential step in closing the nuclear fuel cycle. In order to consume current stockpiles, ceramic uranium dioxide spent nuclear fuel will be subjected to an electrolytic reduction process. The current reduction process employs a platinum anode and a stainless steel alloy 316 cathode in a molten salt bath consisting of LiCl-2wt% Li 2O and occurs at 700°C. A major shortcoming of the existing process is the degradation of the platinum anode under the severely oxidizing conditions encountered during electrolytic reduction. This work investigates alternative anode materials for the electrolytic reduction of uranium oxide. The high temperature and extreme oxidizing conditions encountered in these studies necessitated a unique set of design constraints on the system. Thus, a customized experimental apparatus was designed and constructed. The electrochemical experiments were performed in an electrochemical reactor placed inside a furnace. This entire setup was housed inside a glove box, in order to maintain an inert atmosphere. This study investigates alternative anode materials through accelerated corrosion testing. Surface morphology was studied using scanning electron microscopy. Surface chemistry was characterized using energy dispersive spectroscopy and Raman spectroscopy. Electrochemical behavior of candidate materials was evaluated using potentiodynamic polarization characteristics. After narrowing the number of candidate electrode materials, ferrous stainless steel alloy 316, nickel based Inconel 718 and elemental tungsten were chosen for further investigation. Of these materials only tungsten was found to be sufficiently stable at the anodic potential required for electrolysis of uranium dioxide in molten salt. The tungsten anode and stainless steel alloy 316 cathode electrode system was studied at the required reduction potential for UO2 with varying lithium oxide concentrations. Electrochemical impedance spectroscopy

  3. Synthesis and characterization of graphene nanosheets-cobalt oxide composites as anode material%石墨烯纳米片-氧化亚钴负极材料制备与表征

    Institute of Scientific and Technical Information of China (English)

    柏大伟; 何雨石; 阳炳检; 廖小珍; 马紫峰

    2011-01-01

    采用水热法结合,500℃高温焙烧制备了新型高性能锂离子电池负极材料石墨烯纳米片-氧化亚钴(GNS-CoO)复合材料.采用XRD及TEM等手段对石墨烯纳米片-氧化亚钴复合材料结构和形貌进行表征,并对其电化学性能进行测试.结果表明,石墨烯纳米片-氧化亚钴复合材料的循环性能明显优于氧化亚钴,以200 mA/g进行充放电得到首次放电比容量为1040.2 mAh/g,50次循环后放电比容量为1027.8 mAh/g,显示出良好的循环稳定性.%A graphene nanosheets-CoO(GNS-CoO) composite as a high performance anode material for lithium-ion battery was firstly prepared by a hydrothermal method and then calcined at 500 ℃. The structure, morphology and electrochemical performance of the obtained samples were systematically investigated by X-ray diffraction (XRD), transmission electron microscope (TEM) and electrochemical measurements. The test results show that cycle performance of GNS-CoO is obviously better than cobalt oxide; the specific discharge capacity of GNS-CoO attains to 1 040.2 mAh/g in the first cycle at a current density of 200 mA/g; after 50 cycles, the reversible specific capacity of GNS-CoO can still reach about 1 027.8 mAh/g.

  4. Modeling of the anode surface deformation in high-current vacuum arcs with AMF contacts

    Science.gov (United States)

    Huang, Xiaolong; Wang, Lijun; Deng, Jie; Jia, Shenli; Qin, Kang; Shi, Zongqian

    2016-02-01

    A high-current vacuum arc subjected to an axial magnetic field is maintained in a diffuse status. With an increase in arc current, the energy carried by the arc column to the anode becomes larger and finally leads to the anode temperature exceeding the melting point of the anode material. When the anode melting pool is formed, and the rotational plasma of the arc column delivers its momentum to the melting pool, the anode melting pool starts to rotate and also flow outwards along the radial direction, which has been photographed by some researchers using high-speed cameras. In this paper, the anode temperature and melting status is calculated using the melting and solidification model. The swirl flow of the anode melting pool and deformation of the anode is calculated using the magneto-hydrodynamic (MHD) model with the volume of fraction (VOF) method. All the models are transient 2D axial-rotational symmetric models. The influence of the impaction force of the arc plasma, electromagnetic force, viscosity force, and surface tension of the liquid metal are all considered in the model. The heat flux density injected into the anode and the arc pressure are obtained from the 3D numerical simulation of the high-current vacuum arc using the MHD model, which gives more realistic parameters for the anode simulation. Simulation results show that the depth of the anode melting pool increases with an increase in the arc current. Some droplets sputter out from the anode surface, which is caused by the inertial centrifugal force of the rotational melting pool and strong plasma pressure. Compared with the previous anode melting model without consideration of anode deformation, when the deformation and swirl flow of the anode melting pool are considered, the anode temperature is relatively lower, and just a little more than the melting point of Cu. This is because of liquid droplets sputtering out of the anode surface taking much of the energy away from the anode surface. The

  5. Conductive Polymeric Binder for Lithium-Ion Battery Anode

    Science.gov (United States)

    Gao, Tianxiang

    Tin (Sn) has a high-specific capacity (993 mAhg-1) as an anode material for Li-ion batteries. To overcome the poor cycling performance issue caused by its large volume expansion and pulverization during the charging and discharging process, many researchers put efforts into it. Most of the strategies are through nanostructured material design and introducing conductive polymer binders that serve as matrix of the active material in anode. This thesis aims for developing a novel method for preparing the anode to improve the capacity retention rate. This would require the anode to have high electrical conductivity, high ionic conductivity, and good mechanical properties, especially elasticity. Here the incorporation of a conducting polymer and a conductive hydrogel in Sn-based anodes using a one-step electrochemical deposition via a 3-electrode cell method is reported: the Sn particles and conductive component can be electrochemically synthesized and simultaneously deposited into a hybrid thin film onto the working electrode directly forming the anode. A well-defined three dimensional network structure consisting of Sn nanoparticles coated by conducting polymers is achieved. Such a conductive polymer-hydrogel network has multiple advantageous features: meshporous polymeric structure can offer the pathway for lithium ion transfer between the anode and electrolyte; the continuous electrically conductive polypyrrole network, with the electrostatic interaction with elastic, porous hydrogel, poly (2-acrylamido-2-methyl-1-propanesulfonic acid-co-acrylonitrile) (PAMPS) as both the crosslinker and doping anion for polypyrrole (PPy) can decrease the volume expansion by creating porous scaffold and softening the system itself. Furthermore, by increasing the amount of PAMPS and creating an interval can improve the cycling performance, resulting in improved capacity retention about 80% after 20 cycles, compared with only 54% of that of the control sample without PAMPS. The cycle

  6. Multi-anode ionization chamber

    Energy Technology Data Exchange (ETDEWEB)

    Bolotnikov, Aleksey E. (South Setauket, NY); Smith, Graham (Port Jefferson, NY); Mahler, George J. (Rocky Point, NY); Vanier, Peter E. (Setauket, NY)

    2010-12-28

    The present invention includes a high-energy detector having a cathode chamber, a support member, and anode segments. The cathode chamber extends along a longitudinal axis. The support member is fixed within the cathode chamber and extends from the first end of the cathode chamber to the second end of the cathode chamber. The anode segments are supported by the support member and are spaced along the longitudinal surface of the support member. The anode segments are configured to generate at least a first electrical signal in response to electrons impinging thereon.

  7. Simultaneous Use Of Zr And Mg Anodes In XPS

    Science.gov (United States)

    Allgeyer, D. F.; Pratz, E. H.

    1996-01-01

    Improved x-ray source for x-ray photoelectron spectroscopy (XPS) contains both zirconium anode with beryllium window and magnesium anode with aluminum window. Previously unresolvable peaks of electron-energy spectrum become resolvable. Developed specifically for use in analyzing distributions of chemical constituents in surface layers of specimens of 2219 aluminum alloy and in determining the depths of surface oxide layers and relative proportions of aluminum and oxide in layers. Also used to study chemical constituents of surface layers in other material systems - for example, thin oxide films on silicon-based semiconductor devices, oxide films on alloys, and surface layers affecting adhesion of paints or bonding materials.

  8. Nano structural anodes for radiation detectors

    Energy Technology Data Exchange (ETDEWEB)

    Cordaro, Joseph V.; Serkiz, Steven M.; McWhorter, Christopher S.; Sexton, Lindsay T.; Retterer, Scott T.

    2015-07-07

    Anodes for proportional radiation counters and a process of making the anodes is provided. The nano-sized anodes when present within an anode array provide: significantly higher detection efficiencies due to the inherently higher electric field, are amenable to miniaturization, have low power requirements, and exhibit a small electromagnetic field signal. The nano-sized anodes with the incorporation of neutron absorbing elements (e.g., .sup.10B) allow the use of neutron detectors that do not use .sup.3He.

  9. Full Ceramic Fuel Cells Based on Strontium Titanate Anodes, An Approach Towards More Robust SOFCs

    DEFF Research Database (Denmark)

    Holtappels, Peter; Irvine, J.T.S.; Iwanschitz, B.;

    2013-01-01

    intact and tolerant to redox cycles, cell performance degradation appears linked to the infiltrated electro catalysts. The materials have also been assessed with respect to their electrical and mechanical properties, in order to further evaluate their potential use as anode and anode support layers in...

  10. Anode modification with formic acid: A simple and effective method to improve the power generation of microbial fuel cells

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Weifeng; Cheng, Shaoan, E-mail: shaoancheng@zju.edu.cn; Guo, Jian

    2014-11-30

    Highlights: • Carbon cloth anode is modified with formic acid by a simple and reliable approach. • The modification significantly enhances the power output of microbial fuel cells. • The modified anode surface favors the bacterial attachment and growth on anode. • The electron transfer rate of anode is promoted. - Abstract: The physicochemical properties of anode material directly affect the anodic biofilm formation and electron transfer, thus are critical for the power generation of microbial fuel cells (MFCs). In this work, carbon cloth anode was modified with formic acid to enhance the power production of MFCs. Formic acid modification of anode increased the maximum power density of a single-chamber air-cathode MFC by 38.1% (from 611.5 ± 6 mW/m{sup 2} to 877.9 ± 5 mW/m{sup 2}). The modification generated a cleaner electrode surface and a reduced content of oxygen and nitrogen groups on the anode. The surface changes facilitated bacterial growth on the anode and resulted in an optimized microbial community. Thus, the electron transfer rate on the modified anodes was enhanced remarkably, contributing to a higher power output of MFCs. Anode modification with formic acid could be an effective and simple method for improving the power generation of MFCs. The modification method holds a huge potential for large scale applications and is valuable for the scale-up and commercialization of microbial fuel cells.

  11. Synthesis and Performance of Nano MnO as an Anode Material for Lithium-Ion Batteries%纳米MnO锂离子电池负极材料的制备与性能

    Institute of Scientific and Technical Information of China (English)

    丁朋; 徐友龙; 孙孝飞

    2013-01-01

      以高锰酸钾和抗坏血酸合成的MnC2O4·2H2O为前驱体,通过固相烧结制备了纳米MnO材料.分别采用X射线衍射(XRD)、扫描电子显微镜(SEM)和恒电流充放电技术考察了其晶相结构、颗粒形貌和电化学性能.分析结果表明,该纳米MnO具有面心立方的岩盐结构,结晶度良好.其颗粒是由粒径为50-100 nm的一次颗粒结合而成的二次颗粒,大小约为400-600 nm.当充放电电流密度为46.3 mA·g-1时,纳米 MnO 的首次库仑效率可达68.9%,可逆比容量为679.7 mAh·g-1.在141.1 mA·g-1的电流密度下循环50圈后,比容量由584.5 mAh·g-1降至581.5 mAh·g-1,容量保持率高达99.5%,表现出优异的循环性能.此外,当电流密度增加到494.7 mA·g-1(~2C)时,其比容量依然可达290 mAh·g-1,表现出较好的倍率性能和快速充放电能力.因此,纳米MnO具有比容量高、循环稳定、倍率性能好和安全环保等优点,是一种非常有前景的锂离子电池负极材料.%Transition metal oxides, especial y manganese monoxide (MnO), are being intensively studied as candidate anode materials for next generation lithium-ion batteries in high efficiency energy storage applications such as portable electronics, electric vehicles, and stationary electricity storage. In this paper, the MnC2O4·2H2O precursor, prepared from KMnO4 and ascorbic acid, was heat-treated to synthesize nano MnO by a solid-state reaction approach. X-ray diffraction (XRD) showed that the so-obtained MnO had a rock-salt structure with good crystal inity, and scanning electron microscopy (SEM) indicated that the primary particle size was about 50-100 nm, while the secondary particle size was about 400-600 nm. As an active material for lithium-ion batteries, the nano MnO material delivered a reversible capacity of 679.7 mAh·g-1 with an initial columbic efficiency of 68.9% at a current density of 46.3 mA·g-1. The specific discharge capacity slightly decreased from 584.5 to 581.5 m

  12. Surface Modification of a MCFC Anode by Electrochemical Alloying

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    Considering the properties of the valve metal alloys with specific corrosion resistance and electrocatalytic ac tivity, an investigation was made to examine if nickel-niobium alloy could serve as the anode material for molten carbo nate fuel cell (MCFC). An attempt was made to produce nickel-niobium surface alloy by an electrochemical process in the molten fluorides and to testify its performance required by the MCFC anode. Experimental results indicated that the corrosion resistance as well as polarization performance of the nickel electrode was improved by the surface alloying.As far as the corrosion resistance and polarization performance is concerned, the nickel-niobium surface alloy can be considered as a candidate material for the anode of MCFC.

  13. Results from some anode wire aging tests

    International Nuclear Information System (INIS)

    Using twin setups to test anode wire aging in small gas avalanche tubes, a variety of different gas mixtures were tried and other parameters were varied to study their effects upon the gain drop, nomalized to charge transfer: - 1/Q dI/I. This was found to be quite sensitive to the purity of the gases, and also sensitive to the nominal gain and the gas flow rate. The wire surface material can also significantly affect the aging, as can additives, such as ethanol or water vapor. Certain gas mixtures have been found to be consistent with zero aging at the sensitivity level of this technique

  14. Surface characterization of anodized zirconium for biomedical applications

    Energy Technology Data Exchange (ETDEWEB)

    Sanchez, A. Gomez [Division corrosion - INTEMA, Universidad Nacional del Mar del Plata - CONICET, Juan B. Justo 4302, (7600) Mar del Plata (Argentina); Schreiner, W. [LSI - LANSEN, Departamento de Fisica, UFPR, Curitiba (Brazil); Duffo, G. [Departamento de Materiales, Comision Nacional de Energia Atomica - CONICET, Av. Gral. Paz 1499, (1650) San Martin, Buenos Aires (Argentina); Universidad Nacional de Gral. San Martin, Av. Gral. Paz 1499, (1650) San Martin, Buenos Aires (Argentina); Cere, S., E-mail: smcere@fi.mdp.edu.ar [Division corrosion - INTEMA, Universidad Nacional del Mar del Plata - CONICET, Juan B. Justo 4302, (7600) Mar del Plata (Argentina)

    2011-05-15

    Mechanical properties and corrosion resistance of zirconium make this material suitable for biomedical implants. Its good in vivo performance is mainly due to the presence of a protective oxide layer that minimizes corrosion rate, diminishes the amount of metallic ions released to the biological media and facilitates the osseointegration process. Since the implant surface is the region in contact with living tissues, the characteristics of the surface film are of great interest. Surface modification is a route to enhance both biocompatibility and corrosion resistance of permanent implant materials. Anodizing is presented as an interesting process to modify metal surfaces with good reproducibility and independence of the geometry. In this work the surface of zirconium before and after anodizing in 1 mol/L phosphoric acid solution at a fixed potential between 3 and 30 V, was characterized by means of several surface techniques. It was found that during anodization the surface oxide grows with an inhomogeneous coverage on zirconium surface, modifying the topography. The incorporation of P from the electrolyte to the surface oxide during the anodizing process changes the surface chemistry. After 30 days of immersion in Simulated Body Fluid (SBF) solution, Ca-P rich compounds were present on anodized zirconium.

  15. 石墨烯用作锂离子电池负极材料的电化学性能%Electrochemical performance of graphene sheets as anode material for lithium-ion batteries

    Institute of Scientific and Technical Information of China (English)

    高云雷; 赵东林; 白利忠; 张霁明; 张凡; 谢卫刚

    2012-01-01

    We prepared high quality graphene sheets with a curled morphology consisting of a thin wrinkled paper-like structure and fewer layers (1-4 layers) has been prepared from natural graphite by oxidation, hydrogen reduction at 400 ℃ and ultrasonic treatment. Graphene sheets were investigated as anode material for lithium ion batteries by transmission electron microscopy (TEM), high-resolution TEM, X-ray diffraction, Fourier transform infrared spectroscopy, Raman spectroscopy and a variety of electrochemical testing techniques. The electrochemical performance testing results showed that the first reversible specific capacity of the graphene sheet electrode was as high as 1005 mAh/g at a current density of 0.2 mA/cm2. After 30 cycles the reversible specific capacity was still maintained at 609 mAh/g. Even at a high current density of 1 mA/cm^2, the reversible specific capacity could remain at 576 mAh/g after 30 cycles. These results indicate that the prepared high quality graphene sheets we prepared possess excellent electrochemical performances for lithium storage.%以天然鳞片石墨为原料,通过氧化、离心分离、低温氢气还原和超声分散处理制备了高品质的石墨烯片(1-4层)。采用透射电镜(TEM)、高分辨透射电镜(HRTEM)、傅里叶变换红外光谱(FT-IR)、拉曼光谱、X-射线衍射(XRD)等测试方法对石墨烯的结构和形貌进行了研究。通过恒流充放电、循环伏安法(CV)和交流阻抗(EIS)等手段研究了石墨烯用作锂离子电池负极材料的电化学性能。结果表明在0.2 mA/cm2的电流密度下石墨烯首次可逆比容量为1005 mAh/g,经过30个循环后放电比容量保持在609 mAh/g,在大电流密度下放电容量仍然能保持576 mAh/g,表明石墨烯负极材料具有优异的倍率性能。

  16. Electrochemical performance of nitrogen-doped graphene as anode material for lithium ion batteries%氮掺杂石墨烯作为锂离子电池负极材料的电化学性能

    Institute of Scientific and Technical Information of China (English)

    高云雷; 赵东林; 白利忠; 张霁明; 孔莹

    2012-01-01

      以天然石墨为原料,通过氧化、快速热膨胀和超声分散制备石墨烯。将氧化石墨与三聚氰胺在氮气下950℃反应合成氮掺杂石墨烯。通过扫描电子显微镜(SEM)、透射电子显微镜(TEM)、 X射线衍射(XRD)以及红外光谱(FTIR)、X射线能谱(XPS)等测试方法对氮掺杂石墨烯的形貌、结构进行分析。结果表明,该方法合成了薄层状氮掺杂石墨烯。采用恒流充放电和循环伏安法等手段测试氮掺杂石墨烯、石墨烯和天然石墨作为锂离子电池负极材料的电化学性能,比较研究了三者用作锂离子电池负极材料的电化学性能,结果表明氮掺杂石墨烯负极材料具有优异的电化学能和独特的储锂机制%  Graphene sheets (GSs) have been prepared from natural flake graphite by oxidation, rapid expansion and ultrasonic treatment. Graphene oxide (GO) was further annealed at the presence of melamine at 950 ℃ and transferred into nitrogen-doped grapheme (N-GSs). The samples were characterized via scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS). Electrochemical performances of nitrogen-doped graphene, graphene and graphite as anode materials for lithium ion batteries were investigated using galvanostatic charge-discharge and cyclic voltammetry methods. It was found that the prepared N-GSs exhibited a relatively higher cycling stability and larger specific capacity compared with the pristine nature graphite and GSs. Cyclic voltammograms results indicate that the higher cycling stability may be associated with more structural defects during cycling.

  17. Synthesis of Cu2O/reduced graphene oxide composites as anode materials for lithium ion batteries%锂离子电池用氧化亚铜/石墨烯负极材料的制备

    Institute of Scientific and Technical Information of China (English)

    颜果春; 李新海; 王志兴; 郭华军; 张倩; 彭文杰

    2013-01-01

    A facile way was used to synthesize Cu2O/reduced graphene oxide (rGO) composites with octahedron-like morphology in aqueous solution without any surfactant. TEM images of the obtained Cu2O/rGOs reveal that the Cu2O particles and rGO distribute hierarchically and the primary Cu2O particles are encapsulated well in the graphene nanosheets. The electrochemical performance of Cu2O/rGOs is enhanced compared with bare Cu2O when they are employed as anode materials for lithium ion batteries. The Cu2O/rGO composites maintain a reversible capacity of 348.4 mA⋅h/g after 50 cycles at a current density of 100 mA/g. In addition, the composites retain 305.8 mA⋅h/g after 60 cycles at various current densities of 50, 100, 200, 400 and 800 mA/g.%在不添加表面活性剂的水溶液体系中,采用水合肼作为还原剂制备得到具有八面体形貌的氧化亚铜/石墨烯复合材料。透射电镜分析表明:氧化亚铜颗粒与石墨烯在复合物中呈多层次分布,而且氧化亚铜一次颗粒很好地嵌入在石墨烯层间。相比于纯氧化亚铜,氧化亚铜/石墨烯复合材料作为锂离子电池负极材料的电化学性能得到了显著的改善。在100 mA/g的电流密度下循环50次后,氧化亚铜/石墨烯复合物的可逆比容量高达348.4 mA⋅h/g,同时,在不同倍率下(50,100,200,400,800 mA/g)循环60次后,其可恢复容量仍达305.8 mA⋅h/g。

  18. Preparation of Ce0.8Gd0.2O1.85 Anode Materials by Glicine Nitrate Method%甘氨酸-硝酸盐法制备Ce0.8Gd0.2O1.85阳极材料的研究

    Institute of Scientific and Technical Information of China (English)

    陈秀华; 刘荣辉; 马文会; 王华

    2007-01-01

    The Ce0.8Gd0.2O1.85(GDC82)anode materials were prepared by glycine-nitrate method (GNM). The properties of GDC82 materials were analysized by using X-ray diffraction (XRD), direct current four point probes (DC-FPP) and temperature process reduce (TPR) techniques methods. The total conductivity becomes bigger when the atmosphere changes from air to hydrogen, which greatly increases with the increasing of the temperature and reaches to the maximum value 0.4 S/cm at 850℃. GDC82 and La1-xSrxCr1-yMnyO3-δ(LSCM)anode materials have good chemical compatibility. The catalytic result shows that GDC82 as anode materials has the excellent catalytic property for hydrogen and methane.%采用甘氨酸-硝酸盐法制备了Ce0.8Gd0.2O1.85(GDC82)阳极材料.用XRD, DC-FP,TPR等技术对材料的性能进行表征.GDC82在H2气氛下的总电导率整体增加,且随温度的升高而迅速增加,在850℃达到0.4 S/cm,GDC82与La1-xSrxCr1-yMnyO3-δ(LSCM)阳极材料化学相容性较好,且对氢气和甲烷具有较好的催化氧化效果.

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

    Directory of Open Access Journals (Sweden)

    Mr. Sunil D. Kahar

    2014-07-01

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

  20. The Potential of Acousto-Ultrasonic Techniques for Inspection of Baked Carbon Anodes

    Directory of Open Access Journals (Sweden)

    Moez Ben Boubaker

    2016-07-01

    Full Text Available High quality baked carbon anodes contribute to the optimal performance of aluminum reduction cells. However, the currently decreasing quality and increasing variability of anode raw materials (coke and pitch make it challenging to manufacture the anodes with consistent overall quality. Intercepting faulty anodes (e.g., presence of cracks and pores before they are set in reduction cells and deteriorate their performance is therefore important. This is a difficult task, even in modern and well-instrumented anode plants, because lab testing using core samples can only characterize a small proportion of the anode production due to the costly, time-consuming, and destructive nature of the analytical methods. In addition, these results are not necessarily representative of the whole anode block. The objective of this work is to develop a rapid and non-destructive method for quality control of baked anodes using acousto-ultrasonic (AU techniques. The acoustic responses of anode samples (sliced sections were analyzed using a combination of temporal features computed from AU signals and principal component analysis (PCA. The AU signals were found sensitive to pores and cracks and were able to discriminate the two types of defects. The results were validated qualitatively by submitting the samples to X-ray Computed Tomography (CT scan.

  1. p-Type semiconducting nickel oxide as an efficiency-enhancing anodal interfacial layer in bulk heterojunction solar cells

    Energy Technology Data Exchange (ETDEWEB)

    Irwin, Michael D; Buchholz, Donald B; Marks, Tobin J; Chang, Robert P. H.

    2014-11-25

    The present invention, in one aspect, relates to a solar cell. In one embodiment, the solar cell includes an anode, a p-type semiconductor layer formed on the anode, and an active organic layer formed on the p-type semiconductor layer, where the active organic layer has an electron-donating organic material and an electron-accepting organic material.

  2. Tin-phosphate glass anode for sodium ion batteries

    Directory of Open Access Journals (Sweden)

    Tsuyoshi Honma

    2013-11-01

    Full Text Available The electrochemical property of tin-phosphate (designate as GSPO glass anode for the sodium ion battery was studied. During the first charge process, sodium ion diffused into GSPO glass matrix and due to the reduction of Sn2+ to Sn0 state sodiated tin metal nano-size particles are formed in oxide glass matrix. After the second cycle, we confirmed the steady reversible reaction ∼320 mAh/g at 0–1 V cutoff voltage condition by alloying process in NaxSn4. The tin-phosphate glass is a promising candidate of new anode active material that realizes high energy density sodium ion batteries.

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

    DEFF Research Database (Denmark)

    Abdul Jabbar, Mohammed Hussain

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

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

    Directory of Open Access Journals (Sweden)

    Gerrard Eddy Jai Poinern

    2011-02-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2010-07-01

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

  6. Prelithiated Silicon Nanowires as an Anode for Lithium Ion Batteries

    KAUST Repository

    Liu, Nian

    2011-08-23

    Silicon is one of the most promising anode materials for the next-generation high-energy lithium ion battery (LIB), while sulfur and some other lithium-free materials have recently shown high promise as cathode materials. To make a full battery out of them, either the cathode or the anode needs to be prelithiated. Here, we present a method for prelithiating a silicon nanowire (SiNW) anode by a facile self-discharge mechanism. Through a time dependence study, we found that 20 min of prelithiation loads ∼50% of the full capacity into the SiNWs. Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) studies show that the nanostructure of SiNWs is maintained after prelithiation. We constructed a full battery using our prelithiated SiNW anode with a sulfur cathode. Our work provides a protocol for pairing lithium-free electrodes to make the next-generation high-energy LIB. © 2011 American Chemical Society.

  7. Preparation and electrochemical properties of profiled carbon fiber-supported Sn anodes for lithium-ion batteries

    International Nuclear Information System (INIS)

    Highlights: • A novel architecture of profiled carbon fiber-supported Sn LIB anodes is developed. • This Sn/CF anode exhibits a reversible capacity of 740 mA h g−1 under 0.1 C for 160 cycles with about 92% capacity retention. • The unique structure and plentiful inter-fiber space enhance the electrochemical performance of the designed Sn/CF anode. - Abstract: Tin (Sn)-based lithium-ion battery (LIB) anodes are among the most promising alternatives for conventional graphite anodes due to their high specific capacity and safety. The applications of this anode material are restricted by its fast capacity fading during battery operation and its poor rate capacity. In this study, a novel architecture of profiled carbon fiber supported Sn anodes is developed. The profiled carbon fibers have numerous surface grooves where Sn particles are embedded to provide enough capillary channels for rapid lithium-ion transport and enough inter-fiber space for the accommodation of large Sn volume changes on lithium insertion and extraction. This anode architecture is demonstrated by enhanced electrochemical performance. The reversible capacity of 740 mA h g−1 at 0.1 C after 160 cycles is two times higher than that of the state-of-the-art graphite anode. The simple and applicable synthesis process also provides a new path for designing and preparing carbon fiber-based anode materials with improved electrochemical properties

  8. Strain engineered nanomembranes as anodes for lithium ion batteries

    OpenAIRE

    Deng, Junwen

    2015-01-01

    Lithium ion batteries (LIBs) have attracted considerable interest due to their wide range of applications, such as portable electronics, electric vehicles (EVs) and aerospace applications. Particularly, the emergence of a variety of nanostructured materials has driven the development of LIBs towards the next generation, which is featured with high specific energy and large power density. Herein, rolled-up nanotechnology is introduced for the design of strain-released materials as anodes of...

  9. Structural and Electrochemical Investigation during the First Charging Cycles of Silicon Microwire Array Anodes for High Capacity Lithium Ion Batteries

    OpenAIRE

    Helmut Föll; Jürgen Carstensen; Enrique Quiroga-González

    2013-01-01

    Silicon microwire arrays embedded in Cu present exceptional performance as anode material in Li ion batteries. The processes occurring during the first charging cycles of batteries with this anode are essential for good performance. This paper sheds light on the electrochemical and structural properties of the anodes during the first charging cycles. Scanning Electron Microscopy, X-ray diffractommetry, and fast Fourier transformation impedance spectroscopy are used for the characterization. I...

  10. Composite lithium metal anode by melt infusion of lithium into a 3D conducting scaffold with lithiophilic coating

    OpenAIRE

    Liang, Zheng; Lin, Dingchang; Zhao, Jie; Lu, Zhenda; Liu, Yayuan; Liu, Chong; Lu, Yingying; Wang, Haotian; Yan, Kai; Tao, Xinyong; Cui, Yi

    2016-01-01

    This research paper presents a novel strategy for the fabrication of metal–scaffold composite materials. Particularly, molten lithium metal is infused into a surface-modified three-dimensional matrix with a “lithiophilic” coating. The resulting lithium–scaffold composite was used as battery anodes and exhibited superior performance compared with bare lithium metal anodes. Whereas the emphasis of this study is on lithium anodes, our present work opens up a direction for realization of other me...

  11. Standard test method for laboratory evaluation of magnesium sacrificial anode test specimens for underground applications

    CERN Document Server

    American Society for Testing and Materials. Philadelphia

    1997-01-01

    1.1 This test method covers a laboratory procedure that measures the two fundamental performance properties of magnesium sacrificial anode test specimens operating in a saturated calcium sulfate, saturated magnesium hydroxide environment. The two fundamental properties are electrode (oxidation potential) and ampere hours (Ah) obtained per unit mass of specimen consumed. Magnesium anodes installed underground are usually surrounded by a backfill material that typically consists of 75 % gypsum (CaSO4·2H2O), 20 % bentonite clay, and 5 % sodium sulfate (Na2SO4). The calcium sulfate, magnesium hydroxide test electrolyte simulates the long term environment around an anode installed in the gypsum-bentonite-sodium sulfate backfill. 1.2 This test method is intended to be used for quality assurance by anode manufacturers or anode users. However, long term field performance properties may not be identical to property measurements obtained using this laboratory test. Note 1—Refer to Terminology G 15 for terms used ...

  12. Application of silicon zig-zag wall arrays for anodes of Li-ion batteries

    Science.gov (United States)

    Li, G. V.; Rumyantsev, A. M.; Levitskii, V. S.; Beregulin, E. V.; Zhdanov, V. V.; Terukov, E. I.; Astrova, E. V.

    2016-01-01

    Cyclic tests of anodes based on zigzag wall arrays fabricated by the electrochemical etching and post-anodization treatment of silicon have been performed. Compared with anodes based on nanowires and planar thin films, these structures have several advantages. An ex situ analysis of the morphology and structural transformations in a material subjected to cyclic lithiation was conducted by electron microscopy and micro-Raman spectroscopy. The effect of geometrical parameters and a cycling mode on the degradation rate was studied. It is shown that a significant rise in the cycle life of the anode can be obtained by the restriction of the inserted amount of lithium. The anode, subjected to galvanostatic cycling at a rate С/2.8 at a limited charge capacity of 1000 mA · h g-1, demonstrates no degradation after 1200 cycles.

  13. Electrochemical behaviors of anodic alumina sealed by Ce-Mo in NaCl solutions

    Institute of Scientific and Technical Information of China (English)

    TIAN Lian-peng; ZHAO Xu-hui; ZHAO Jing-mao; ZHANG Xiao-feng; ZUO Yu

    2006-01-01

    The elimination of toxic materials in sealing methods for anodic films on 1070 aluminum alloy was studied. The new process uses chemical treatments in cerium solution and an electrochemical treatment in a molybdate solution. Potentiodynamic polarization and electrochemical impedance spectroscopy(EIS) were used to study the influences of sealing methods on the corrosion behavior of anodic films in NaCl solutions. The results show that the Ce-Mo sealing makes the surface structure and morphology of anodic films uniform and compact. Ce and Mo produce a cooperative effect to improve the corrosion resistance of anodic films. Anodic films sealed by Ce-Mo provide high corrosion resistance both in acidic and basic solutions.

  14. Ellipsometry of anodic film growth

    Energy Technology Data Exchange (ETDEWEB)

    Smith, C.G.

    1978-08-01

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

  15. Anodic dissolution of metals in ionic liquids

    Directory of Open Access Journals (Sweden)

    Andrew P. Abbott

    2015-12-01

    Full Text Available The anodic dissolution of metals is an important topic for battery design, material finishing and metal digestion. Ionic liquids are being used in all of these areas but the research on the anodic dissolution is relatively few in these media. This study investigates the behaviour of 9 metals in an ionic liquid [C4mim][Cl] and a deep eutectic solvent, Ethaline, which is a 1:2 mol ratio mixture of choline chloride and ethylene glycol. It is shown that for the majority of metals studied a quasi-passivation of the metal surface occurs, primarily due to the formation of insoluble films on the electrode surface. The behaviour of most metals is different in [C4mim][Cl] to that in Ethaline due in part to the differences in viscosity. The formation of passivating salt films can be decreased with stirring or by increasing the electrolyte temperature, thereby increasing ligand transport to the electrode surface.

  16. Alternate Anodes for the Electrolytic Reduction of UO2

    Science.gov (United States)

    Merwin, Augustus; Chidambaram, Dev

    2015-01-01

    The electrolytic reduction process of UO2 employs a platinum anode and a stainless steel cathode in molten LiCl-LiO2 maintained at 973 K (700 °C). The degradation of platinum under the severely oxidizing conditions encountered during the process is an issue of concern. In this study, Inconel 600 and 718, stainless steel alloy 316, tungsten, nickel, molybdenum, and titanium, were investigated though electrochemical polarization techniques, electron microscopy, Raman spectroscopy, and X-ray photoelectron spectroscopy to serve as potential anode materials. Of the various materials investigated, only tungsten exhibited sufficient stability at the required potential in the molten electrolyte. Tungsten anodes were further studied in molten LiCl-LiO2 electrolyte containing 2, 4, and 6 wt pct of Li2O. In LiCl-2 wt pct Li2O tungsten was found to be sufficiently stable to both oxidation and microstructural changes and the stability is attributed to the formation of a lithium-intercalated tungsten oxide surface film. Increase in the concentration of Li2O was found to lead to accelerated corrosion of the anode, in conjunction with the formation of a peroxotungstate oxide film.

  17. Surface nanotopography of an anodized Ti–6Al–7Nb alloy enhances cell growth

    Energy Technology Data Exchange (ETDEWEB)

    Huang, Her-Hsiung [Department of Dentistry, National Yang-Ming University, Taipei 112, Taiwan (China); Graduate Institute of Basic Medical Science, China Medical University, Taichung 404, Taiwan (China); Department of Biomedical Informatics, Asia University, Taichung 413, Taiwan (China); Department of Stomatology, Taipei Veterans General Hospital, Taipei 112, Taiwan (China); Wu, Chia-Ping [Institute of Oral Biology, National Yang-Ming University, Taipei 112, Taiwan (China); Sun, Ying-Sui [Department of Dentistry, National Yang-Ming University, Taipei 112, Taiwan (China); Yang, Wei-En [Institute of Oral Biology, National Yang-Ming University, Taipei 112, Taiwan (China); Lee, Tzu-Hsin, E-mail: biomaterials@hotmail.com [School of Dentistry, Chung Shan Medical University, Taichung 402, Taiwan (China); Oral Medicine Center, Chung Shan Medical University Hospital, Taichung 402, Taiwan (China)

    2014-12-05

    Highlights: • An electrochemical anodization was applied to α/β-type Ti–6Al–7Nb alloy surface. • Anodized surface had a nontoxic nanoporous topography. • Anodized surface increased proteins adsorption due to nanotopography. • Anodized surface enhanced cell growth due to nanotopography. • Electrochemical anodization has potential as implant surface treatment. - Abstract: The α/β-type Ti–6Al–7Nb alloy is a potential replacement for α/β-type Ti–6Al–4V alloy, which is widely used in biomedical implant applications. The biological response to implant material is dependent on the surface characteristics of the material. In the present study, a simple and fast process was developed to perform an electrochemical anodization treatment on Ti–6Al–7Nb alloy. The proposed process yielded a thin surface nanotopography, which enhanced cell growth on the Ti–6Al–7Nb alloy. The surface characteristics, including the morphology, wettability, and protein adsorption, were investigated, and the cytotoxicity was evaluated according to International Organization for Standardization 10993-5 specifications. Cell adhesion of human bone marrow mesenchymal stem cells on the test specimens was observed via fluorescence microscopy and scanning electron microscopy. The anodization process produced a surface nanotopography (pore size <100 nm) on anodized Ti–6Al–7Nb alloy, which enhanced the wettability, protein adsorption, cell adhesion, cell migration, and cell mineralization. The results showed that the surface nanotopography produced using the proposed electrochemical anodization process enhanced cell growth on anodized Ti–6Al–7Nb alloy for implant applications.

  18. Surface nanotopography of an anodized Ti–6Al–7Nb alloy enhances cell growth

    International Nuclear Information System (INIS)

    Highlights: • An electrochemical anodization was applied to α/β-type Ti–6Al–7Nb alloy surface. • Anodized surface had a nontoxic nanoporous topography. • Anodized surface increased proteins adsorption due to nanotopography. • Anodized surface enhanced cell growth due to nanotopography. • Electrochemical anodization has potential as implant surface treatment. - Abstract: The α/β-type Ti–6Al–7Nb alloy is a potential replacement for α/β-type Ti–6Al–4V alloy, which is widely used in biomedical implant applications. The biological response to implant material is dependent on the surface characteristics of the material. In the present study, a simple and fast process was developed to perform an electrochemical anodization treatment on Ti–6Al–7Nb alloy. The proposed process yielded a thin surface nanotopography, which enhanced cell growth on the Ti–6Al–7Nb alloy. The surface characteristics, including the morphology, wettability, and protein adsorption, were investigated, and the cytotoxicity was evaluated according to International Organization for Standardization 10993-5 specifications. Cell adhesion of human bone marrow mesenchymal stem cells on the test specimens was observed via fluorescence microscopy and scanning electron microscopy. The anodization process produced a surface nanotopography (pore size <100 nm) on anodized Ti–6Al–7Nb alloy, which enhanced the wettability, protein adsorption, cell adhesion, cell migration, and cell mineralization. The results showed that the surface nanotopography produced using the proposed electrochemical anodization process enhanced cell growth on anodized Ti–6Al–7Nb alloy for implant applications

  19. [Vernier Anode Design and Image Simulation].

    Science.gov (United States)

    Zhao, Ai-rong; Ni, Qi-liang; Song, Ke-fei

    2015-12-01

    Based-MCP position-sensitive anode photon-counting imaging detector is good at detecting extremely faint light, which includes micro-channel plate (MCP), position-sensitive anode and readout, and the performances of these detectors are mainly decided by the position-sensitive anode. As a charge division anode, Vernier anode using cyclically varying electrode areas which replaces the linearly varying electrodes of wedge-strip anode can get better resolution and greater electrode dynamic range. Simulation and design of the Vernier anode based on Vernier's decode principle are given here. Firstly, we introduce the decode and design principle of Vernier anode with nine electrodes in vector way, and get the design parameters which are the pitch, amplitude and the coarse wavelength of electrode. Secondly, we analyze the effect of every design parameters to the imaging of the detector. We simulate the electron cloud, the Vernier anode and the detector imaging using Labview software and get the relationship between the pitch and the coarse wavelength of the anode. Simultaneously, we get the corresponding electron cloud for the designing parameters. Based on the result of the simulation and the practical machining demand, a nine electrodes Vernier anode was designed and fabricated which has a pitch of 891 µm, insulation width of 25 µm, amplitude of 50 µm, coarse pixel numbers of 5. PMID:26964205

  20. Electrocatalysis of carbon anode in aluminium electrolysis

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    The anodic overvoltage of the carbon anode in aluminum electrolysis isof the order of 0.6 V at normal current densities. However, it can be reduced somewhat by doping the anode carbon with various inorganic compounds. A new apparatus was designed to improve the precision of overvoltage measurements. Anodes were doped with MgAl2O4 and AlF3 both by impregnation of the coke and by adding powder, and the measured overvoltage was compared with that of undoped samples. For prebake type anodes baked at around 1150 oC, the anodic overvoltage was reduced by 40-60 mV, and for Soderberg type anodes, baked at 950 oC, by 60-80 mV.