Nano-sized copper tungstate thin films as positive electrodes for rechargeable Li batteries

Nano-sized CuWO₄ thin films have been fabricated by radio-frequency (R.F.) sputtering deposition, and are used as positive electrode with both LiClO₄ liquid electrolyte and LiPON solid electrolyte in rechargeable lithium batteries. An initial discharge capacity of 192 and 210 mAh/g is obtainable for CuWO₄ film electrode with and without coated LiPON in liquid electrolyte, respectively. An all-solid-state cell with Li/LiPON/CuWO₄ layers shows a high-volume rate capacity of 145 μAh/cm² μm in first discharge, and overcomes the unfavorable electrochemical degradation observed in liquid electrolyte system. A two-step reactive mechanism is investigated by both transmission electron microscopy and selected area electron diffraction techniques. Apart from the extrusion and injection of Cu²⁺/Cu⁰, additional capacity can be achieved by the reversible reactivity of (WO₄)²⁻ framework. The chemical diffusion coefficients of Li intercalation/deintercalation are estimated by cyclic voltammetry. Nano-CuWO₄ thin film is expected to be a promising positive electrode material for high-performance rechargeable thin-film lithium batteries.     

Electrochemical impedance characterization of FeSn2 electrodes for Li-ion batteries

This work reports the electrochemical characterization of a micro-scale FeSn₂ electrode in a lithium battery. The electrode is proposed as anode material for advanced lithium ion batteries due to its characteristics of high capacity (500 mAh g⁻¹) and low working voltage (0.6 V vs. Li). The electrochemical alloying process is studied by cyclic voltammetry and galvanostatic cycling while the interfacial properties are investigated by electrochemical impedance spectroscopy. The impedance measurements in combination with the galvanostatic cycling tests reveal relatively low overall impedance values and good electrochemical performance for the electrode, both in terms of delivered capacity and cycling stability, even at the higher C-rate regimes.     

Electrochemical properties of TiP2O7 and LiTi2(PO4)3 as anode material for lithium ion battery with aqueous solution electrolyte

Some polyanionic compounds, e.g. TiP₂O₇ and LiTi₂(PO₄)₃ with 3D framework structure were proposed to be used as anodes of lithium ion battery with aqueous electrolyte. The cyclic voltammetry properties TiP₂O₇ and LiTi₂(PO₄)₃ suggested that Li-ion de/intercalation reaction can occur without serious hydrogen evolution in 5 M LiNO₃ aqueous solution. The TiP₂O₇ and LiTi₂(PO₄)₃ give capacities of about 80 mAh/g between potentials of −0.50 V and 0 V (versus SHE) and 90 mAh/g between −0.65 V and −0.10 V (versus SHE), respectively. A test cell consisting of TiP₂O₇/5 M LiNO₃/LiMn₂O₄ delivers approximately 42 mAh/g (weight of cathode and anode) at average voltage of 1.40 V, and LiTi₂(PO₄)₃/5 M LiNO₃/LiMn₂O₄ delivers approximately 45 mAh/g at average voltage of 1.50 V. Both as-assembled cells suffered from short cycle life. The capacity fading may be related to deterioration of anode material.     

Electrochemical properties of microwave irradiated synthesis of poly(3,4-ethylenedioxythiophene)/V2O5 nanocomposites as cathode materials for rechargeable lithium batteries

A series of poly(3,4-ethylenedioxythiophene) (PEDOT)/V₂O₅ nanocomposites are prepared via the redox intercalative polymerization reaction of 3,4-ethylenedioxythiophene (EDOT) monomer and crystalline V₂O₅ within 10 min by using rapid 2.45 GHz microwave irradiation with full power (800 W). The unique properties of the resultant nanocomposites are investigated by various characterization techniques using powder XRD, TGA/DTA and four-point probe conductivity analysis supports the intercalation of polymer nanosheet between V₂O₅ layers leading to enhanced bi-dimensionality. X-ray photoelectron spectroscopy analysis clearly shows the presence of mixed valent V⁴⁺/V⁵⁺ in the V₂O₅ framework after the redox intercalative polymerization which also confirms charge transfer from the polymer to the V₂O₅ framework. The application potential of these composites as cathode materials in rechargeable lithium batteries is also demonstrated by the electrochemical intercalation of lithium into the PEDOT/V₂O₅ nanocomposites, where an enhancement in the discharge capacity (370 mAh/g) is observed compared to that of crystalline V₂O₅.     

Synthesis and electrochemical properties of Co-doped Li3V2(PO4)3 cathode materials for lithium-ion batteries

Co-doped Li₃V_2−xCo_x(PO₄)₃/C (x = 0.00, 0.03, 0.05, 0.10, 0.13 or 0.15) compounds were prepared via a solid-state reaction. The Rietveld refinement results indicated that single-phase Li₃V_2−xCo_x(PO₄)₃/C (0 ≤ x ≤ 0.15) with a monoclinic structure was obtained. The X-ray photoelectron spectroscopy (XPS) analysis revealed that the cobalt is present in the +2 oxidation state in Li₃V_2−xCo_x(PO₄)₃. XPS studies also revealed that V⁴⁺ and V³⁺ ions were present in the Co²⁺-doped system. The initial specific capacity decreased as the Co-doping content increased, increasing monotonically with Co content for x > 0.10. Differential capacity curves of Li₃V_2−xCo_x(PO₄)₃/C compounds showed that the voltage peaks associated with the extraction of three Li⁺ ions shifted to higher voltages with an increase in Co content, and when the Co²⁺-doping content reached 0.15, the peak positions returned to those of the unsubstituted Li₃V₂(PO₄)₃ phase. For the Li₃V_1.85Co_0.15(PO₄)₃/C compound, the initial capacity was 163.3 mAh/g (109.4% of the initial capacity of the undoped Li₃V₂(PO₄)₃) and 73.4% capacity retention was observed after 50 cycles at a 0.1 C charge/discharge rate. The doping of Co²⁺into V sites should be favorable for the structural stability of Li₃V_2−xCo_x(PO₄)₃/C compounds and so moderate the volume changes (expansion/contraction) seen during the reversible Li⁺ extraction/insertion, thus resulting in the improvement of cell cycling ability.     

Polyvinylpyrrolidone-assisted synthesis of microscale C-LiFePO4 with high tap density as positive electrode materials for lithium batteries

Carbon-coated LiFePO₄ (C-LiFePO₄) with micron particle size (6 μm) and high tap density (1.6 g cm⁻³) was prepared from spherical FePO₄·2H₂O powder via the co-precipitation method. The C-LiFePO₄ powder was calcined at temperatures between 650 and 800 °C. The 6 μm C-LiFePO₄ prepared at 800 °C exhibited an excellent rate capability, delivering 150 mAh g⁻¹ on discharge at the 0.1 C-rate and 108 mAh g⁻¹ at the 5 C-rate. The volumetric capacity of the 6 μm C-LiFePO₄ corresponded to 225 mAh cm⁻³, since the large secondary particles (6 μm) C-LiFePO₄ sufficiently allowed tight packing of the particles. The 6 μm C-LiFePO₄ powder with high tap density makes an attractive positive electrode candidate for lithium-ion batteries designed for high energy density.     

A promising sol-gel route based on citric acid to synthesize Li3V2(PO4)3/carbon composite material for lithium ion batteries

Li₃V₂(PO₄)₃/carbon composite material was synthesized by a promising sol-gel route based on citric acid using V₂O₅ powder as a vanadium source. Citric acid acts not only as a chelating reagent but also as a carbon source, which enhance the conductivity of the composite material and hinder the growth of Li₃V₂(PO₄)₃ particles. The structure and morphology of the sample were characterized by TG, XRD and TEM measurements. XRD results reveal that Li₃V₂(PO₄)₃/carbon was successfully synthesized and has a monoclinic structure with space group P2₁/n. TEM images show Li₃V₂(PO₄)₃ particles are about 45 nm in diameter embeded in carbon networks. Galvanostatic charge/discharge and cyclic voltammetry measurements were used to study its electrochemical behaviors which indicate the reversibility of the lithium extraction/insertion processes. Li₃V₂(PO₄)₃/carbon performed in a voltage window (3.0-4.8 V) exhibits higher discharge capacity, better cycling stability and its discharge capacity maintains about 167.6 mAh/g at a current density of 28 mA/g after 50 cycles.     

Preparation and electrochemical performance studies on Cr-doped Li3V2(PO4)3 as cathode materials for lithium-ion batteries

Cr-doped Li₃V_2−xCr_x(PO₄)₃/C (x = 0, 0.05, 0.1, 0.2, 0.5, 1) compounds have been prepared using sol–gel method. The Rietveld refinement results indicate that single-phase Li₃V_2−xCr_x(PO₄)₃/C with monoclinic structure can be obtained. Although the initial specific capacity decreased with Cr content at a lower current rate, both cycle performance and rate capability have excited improvement with moderate Cr-doping content in Li₃V_2−xCr_x(PO₄)₃/C. Li₃V_1.9Cr_0.1(PO₄)₃/C compound presents an initial capacity of 171.4 mAh g⁻¹ and 78.6% capacity retention after 100 cycles at 0.2C rate. At 4C rate, the Li₃V_1.9Cr_0.1(PO₄)₃/C can give an initial capacity of 130.2 mAh g⁻¹ and 10.8% capacity loss after 100 cycles where the Li₃V₂(PO₄)₃/C presents the initial capacity of 127.4 mAh g⁻¹ and capacity loss of 14.9%. Enhanced rate and cyclic capability may be attributed to the optimizing particle size, carbon coating quality, and structural stability during the proper amount of Cr-doping (x = 0.1) in V sites.     

Low temperature solid-state synthesis routine and mechanism for Li3V2(PO4)3 using LiF as lithium precursor

Monoclinic lithium vanadium phosphate, Li₃V₂(PO₄)₃, has been successfully synthesized using LiF as lithium source. The one-step reaction with stoichiometric composition and relative lower sintering temperature (700 °C) has been used in our experimental processes. The solid-state reaction mechanism using LiF as lithium precursor has been studied by X-ray diffraction and Fourier transform infrared spectra. The Rietveld refinement results show that in our product sintered at 700 °C no impurity phases of VPO₄, Li₅V(PO₄)₂F₂, or LiVPO₄F can be detected. The solid-state reaction using Li₂CO₃ as Li-precursor has also been carried out for comparison. X-ray diffraction patterns indicate that impurities as Li₃PO₄ can be found in the product using Li₂CO₃ as Li-precursor unless the sintering temperatures are higher than 850 °C. An abrupt particle growth (about 2 μm) has also been observed by scanning electron microscope for the samples sintered at higher temperatures, which can result in a poor cycle performance. The product obtained using LiF as Li-precursor with the uniform flake-like particles and smaller particle size (about 300 nm) exhibits the better performance. At the 50th cycle, the reversible specific capacities for Li₃V₂(PO₄)₃ measured between 3 and 4.8 V at 1C rate are found to approach 147.1 mAh/g (93.8% of initial capacity). The specific capacity of 123.6 mAh/g can even be hold between 3 and 4.8 V at 5C rate.     

Hydrothermal synthesis and rate capacity studies of Li3V2(PO4)3 nanorods as cathode material for lithium-ion batteries

It is an effective method by synthesizing one-dimensional nanostructure to improve the rate performances of cathode materials for Li-ion batteries. In this paper, Li₃V₂(PO₄)₃ nanorods were successfully prepared by hydrothermal reaction method. The structure, composition and shape of the prepared were characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scan electron microscope (SEM) and transmission electron microscope (TEM), respectively. The data indicate the as-synthesis powders are defect-rich nanorods and the sizes are the length of several hundreds of nanometers to 1 μm and the diameter of about 60 nm. The preferential growth direction of the prepared material was the [1 2 0]. The electrodes consisting of the Li₃V₂(PO₄)₃ nanorods show the better discharge capacities at high rates over a potential range of 3.0-4.6 V. These results can be attributed to the shorter distance of electron transport and the fact that ion diffusion in the electrode material is limited by the nanorod radius. All these results indicate that the resulting Li₃V₂(PO₄)₃ nanorods are promising cathode materials in lithium-ion batteries.     

Fractal study of LiMn2O4 film electrode surface for lithium batteries application

Fractal structure of a LiMn₂O₄ film electrode has been investigated and its fractal dimensions was determined using different electrochemical techniques, viz. cyclic voltammetry and chronoamperometry. The results obtained from both these methods are in good agreement indicating the reliability of the estimated D_f. The fractal study of the LiMn₂O₄ film electrode suggests a complex surface with high fractal dimension. In addition, length scales of the electrode surface were also calculated.     

Synthesis and electrochemical characterization of nano-CeO2-coated nanostructure LiMn2O4 cathode materials for rechargeable lithium batteries

LiMn₂O₄ spinel cathode materials were coated with 0.5, 1.0, and 1.5 wt.% CeO₂ by a polymeric process, followed by calcination at 850 °C for 6 h in air. The surface-coated LiMn₂O₄ cathode materials were physically characterized using X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and X-ray photoelectron microscopy (XPS). XRD patterns of CeO₂-coated LiMn₂O₄ revealed that the coating did not affect the crystal structure or the Fd3m space group of the cathode materials compared to uncoated LiMn₂O₄. The surface morphology and particle agglomeration were investigated using SEM, TEM image showed a compact coating layer on the surface of the core materials that had average thickness of about 20 nm. The XPS data illustrated that the CeO₂ completely coated the surface of the LiMn₂O₄ core cathode materials. The galvanostatic charge and discharge of the uncoated and CeO₂-coated LiMn₂O₄ cathode materials were measured in the potential range of 3.0-4.5 V (0.5 C rate) at 30 °C and 60 °C. Among them, the 1.0 wt.% of CeO₂-coated spinel LiMn₂O₄ cathode satisfies the structural stability, high reversible capacity and excellent electrochemical performances of rechargeable lithium batteries.     

Electrochemical Quartz Microbalance characterization of Ni(OH)2-based thin film electrodes

The use of the Electrochemical Quartz Crystal Microbalance (EQCM) to study the proton intercalation performance of thin film Ni(OH)₂ layers, nowadays widely used as cathode electrode material in rechargeable Ni(OH)₂-based battery systems such as NiMH and NiCd, is reviewed. In addition, the impact of incorporating foreign metals in these layers on the electrochemical performance will be highlighted.Using EQCM much information can be obtained, as both the electrochemical response and accompanying mass changes can be measured simultaneously. EQCM was extensively used to investigate the effect of the conditions on the formation of Ni(OH)₂ thin layers, the α-to-β modification changes and the details of the redox mechanism. The proposed redox mechanisms differ in whether H⁺ or OH⁻ is transferred, the reactants and/or products are hydrated and cations from the solution take part in the reaction.By incorporation of other metals in the structure, the characteristics of thin Ni(OH)₂ layers can be tuned. This affects the oxidation and reduction potential, the reversibility, the stability of the structure and the oxygen evolution side reaction. Co²⁺ and Fe²⁺ were shown to replace Ni-sites in the hydrous oxide lattice, thereby forming very dense structures with higher stability. However, structural changes still occur in most cases. Due to this inhomogeneity, the layers are usually a combination of different structures, depending on the distribution of the incorporated metal(s). Suppression of the oxygen evolution reaction is reported for Co, Pb, Pd, Zn and Mn. The effects of Co and Mn are shown to depend on the incorporated amount. Co shifts the standard redox potential for the oxygen evolution reaction towards more cathodic potentials and decreases the oxygen overpotential significantly. Light-weight rare-earth elements also catalyze the oxygen evolution reaction.     

Three-dimensional porous amorphous SnO2 thin films as anodes for Li-ion batteries

Three-dimensional (3D) porous amorphous SnO₂ thin films were deposited on Ni foam substrates by Electrostatic Spray Deposition (ESD) technique as anodes for Li-ion batteries. These films display good capacity retention of 94.8% after 100 cycles at 0.5 C and rate capability of 362 mAh/g at 10 C. The improved performance originates from the fact that the 3D porous structure offers a “buffer zone” to accommodate the large volume change during cycling, and the foam-like substrate maximizes the contact area between electrode and electrolyte. The facile ESD method can be potentially extended to prepare other 3D porous functional materials.     

Antimonides (FeSb2, CrSb2) with orthorhombic structure and their nanocomposites for rechargeable Li-ion batteries

Intermetallic FeSb₂ and CrSb₂ and their nanocomposites (FeSb₂/C and Sb/Cr₃C₂/C) were prepared using solid-state routes, such as heat-treatment and high-energy mechanical milling, in order to enhance the electrochemical properties of Sb. These electrodes were tested as anode materials for rechargeable Li-ion batteries. The reaction mechanism of intermetallic FeSb₂ and CrSb₂ was investigated using ex situ X-ray diffraction and high resolution transmission electron microscopy. The FeSb₂/C and Sb/Cr₃C₂/C nanocomposite electrodes exhibited greatly enhanced electrochemical behaviors compared to the FeSb₂ and CrSb₂ electrodes. Additionally, the Sb/Cr₃C₂/C nanocomposite electrode showed a better electrochemical performance than the FeSb₂/C nanocomposite electrode.     

Preparation and electrochemical properties of Cr-doped Li9V3(P2O7)3(PO4)2 as cathode materials for lithium-ion batteries

Cr-doped Li₉V_3−xCr_x(P₂O₇)₃(PO₄)₂ (x = 0.0–0.5) compounds have been prepared using sol–gel method. The Rietveld refinement results indicate that single-phase Li₉V_3−xCr_x(P₂O₇)₃(PO₄)₂ (x = 0.0–0.5) with trigonal structure can be obtained. Although the initial specific capacity decreased with Cr content at a lower current rate, both cycle performance and rate capability have excited improvement with moderate Cr-doping content. Li₉V_2.8Cr_0.2(P₂O₇)₃(PO₄)₂ compound presents the good electrochemical rate and cyclic ability. The enhancement of rate and cyclic capability may be attributed to the optimizing particle size, morphologies, and structural stability during the proper amount of Cr-doping (x = 0.2) in V sites.     

Optimum synthesis of Li2Fe1−xMnxSiO4/C cathode for lithium ion batteries

Li₂Fe_1−xMn_xSi0₄/C cathode materials were synthesized by mechanical activation-solid-state reaction. The effects of Mn-doping content, roasting temperature, soaking time and Li/Si molar ratio on the physical properties and electrochemical performance of the Li₂Fe_1−xMn_xSi0₄/C composites were investigated. The materials were characterized by X-ray diffraction (XRD) and scanning electron microscope (SEM), charge-discharge tests and AC impedance measurements. SEM images suggest that the morphology of the Li₂Fe_1−xMn_xSi0₄/C composite is sensitive to the reaction temperature. Samples synthesized at different temperatures have different extent of agglomeration. Being charged-discharged at C/32 between 1.5 and 4.8 V, the Li₂Fe_0.9Mn_0.1Si0₄/C synthesized at the optimum conditions shows good electrochemical performances with an initial discharge capacity of 158.1 mAh g⁻¹ and a capacity retention ratio of 94.3% after 30 cycles. AC impendence investigation shows Li₂Fe_0.9Mn_0.1SiO₄/C have much lower resistance of electrode/electrolyte interface than Li₂FeSiO₄/C.     

Structural modification of Li[Li0.27Co0.20Mn0.53]O2 by lithium extraction and its electrochemical property as the positive electrode for Li-ion batteries

In our previous report, we have synthesized Li₂MnO₃-LiCoO₂ solid solutions and have investigated electrochemical properties [J.-M. Kim, T. Sho, N. Kumagai, Electrochem. Commun. 9 (2007) 103]. These materials have showed a long charge plateau at above 4.5 V during the first charge, which disappears with the subsequent cycles. This phenomenon is usually observed in Li₂MnO₃ and Li₂MnO₃-LiMeO₂ system (Me = Ni_1/2Mn_1/2 [Z. Lu, D.D. MacNeil, J.R. Dahn, Electrochem. Solid State Lett. 4 (2001) 191], Co [K. Numata, C. Sakaki, S. Yamanaka, Solid State Ionics 117 (1999) 257; Y.J. Park, Y.-S. Hong, X. Wu, M.K. Kim, K.S. Ryu, S.H. Chang, J. Electrochem. Soc. 151 (2004) A720], Fe [M. Tabuchi, A. Nakashima, H. Shigemura, K. Ado, H. Kobayashi, H. Sakaebe, H. Kageyama, T. Nakamura, M. Kohzaki, A. Hirano, R. Kanno, J. Electrochem. Soc. 149 (2002) A509], or Cr [B. Ammundsen, J. Paulsen, Adv. Mater. 13 (2001) 943]). In this study, we investigate the relationship between the first lithium extraction process and the electrochemical property of the synthesized Li[Li_0.27Co_0.2Mn_0.53]O₂ material. The crystal structure and electrochemical performance of the synthesized Li[Li_0.27Co_0.20Mn_0.53]O₂ are modified by the Li⁺ extraction.     

Preparation of micro-dot electrodes of LiCoO2 and Li4Ti5O12 for lithium micro-batteries

Fabrications of micro-dot electrodes of LiCoO₂ and Li₄Ti₅O₁₂ on Au substrates were demonstrated using a sol-gel process combined with a micro-injection technology. A typical size of prepared dots was about 100 μm in diameter, and the dot population on the substrate was 2400 dots cm⁻². The prepared LiCoO₂ and Li₄Ti₅O₁₂ micro-dot electrodes were characterized with scanning electron microscopy, X-ray diffraction, micro-Raman spectroscopy, and cyclic voltammetry. The prepared LiCoO₂ and Li₄Ti₅O₁₂ micro-dot electrodes were evaluated in an organic electrolyte as cathode and anode for lithium micro-battery, respectively. The LiCoO₂ micro-dot electrode exhibited reversible electrochemical behavior in a potential range from 3.8 to 4.2 V versus Li/Li⁺, and the Li₄Ti₅O₁₂ micro-dot electrode showed sharp redox peaks at 1.5 V.     

Hydrothermal synthesis of Li(Ni1/3Co1/3Mn1/3)O2 for lithium rechargeable batteries

Ultrafine powders of Li(Ni_1/3Co_1/3Mn_1/3)O₂ cathode materials for lithium-ion secondary batteries were prepared under mild hydrothermal conditions. The influence of the molar ratio of Li/(Ni + Co + Mn) was studied. The products were investigated by XRD, TEM and EDS. The final products were found to be well crystallized Li(Ni_1/3Co_1/3Mn_1/3)O₂ with an average particle size of about 10 nm.