Synthesis of high-voltage cathode material using the Taylor-Couette flow-based co-precipitation method.

LiNi0.5Mn1.5O4 (LNMO), a next-generation high-voltage battery material, is promising for high-energy-density and power-density lithium-ion secondary batteries. However, rapid capacity degradation occurs due to problems such as the elution of transition metals and the generation of structural distortion during cycling. Herein, a new LNMO material was synthesized using the Taylor-Couette flow-based co-precipitation method. The synthesized LNMO material consisted of secondary particles composed of primary particles with an octahedral structure and a high specific surface area. In addition, the LNMO cathode material showed less structural distortion and cation mixing as well as a high cyclability and rate performance compared with commercially available materials.

Effect of Nanoparticles in LiFePO4 Cathode Material Using Organic/Inorganic Composite Solid Electrolyte for All-Solid-State Batteries.

Herein, we report the effect of using nanoparticles of LiFePO4 on the electrochemical properties of all-solid-state batteries (ASSBs) with a solid electrolyte. LiFePO4 (LFP) cathode materials are promising cathode materials in polymer-based composite solid electrolytes because of their limited electrochemical window range. However, LFP cathodes exhibit poor electric conductivity and sluggish lithium ion diffusion. In addition, there is a disadvantage in that the interfacial resistance increases due to poor contact between the LFP cathode material and the solid electrolyte when composing the composite cathode. The nano-sized LFP cathode material increases the contact area between solid electrolyte in the positive electrode and enhances lithium ion diffusion. Therefore, the structural differences and electrochemical performance of these nanoscale LFP cathode materials in the ASSB were studied by X-ray diffraction, scanning electron microscopy, and electrochemical analysis.

Effect of a self-assembling La2(Ni0.5Li0.5)O4 and amorphous garnet-type solid electrolyte composite on a layered cathode material in all-solid-state batteries.

In this article, we report the effect of a Li6.75La3Zr2Al0.25O12 (LLZAO) composite Li(Ni0.8Co0.1Mn0.1)O2 (NCM811) cathode material on the performance of all-solid-state batteries (ASSBs) with oxide-based organic/inorganic hybrid solid electrolytes. The layered structure of Ni-rich cathode material Li(Ni x Co(1-x)/2Mn(1-x)/2)O2 (x > 0.6) (NCM) exhibiting a high specific capacity is among the suitable cathode materials for next-generation energy storage systems, particularly electric vehicles and portable devices for all-solid-state batteries. However, the ASSBs present a problem-the resistance at the interface between a cathode and solid electrolyte is larger than that with a liquid electrolyte because of point contact. To solve this problem, using a simultaneous co-precipitation method, we composited various amounts of LLZAO material and an ion conducting material on the cathode material's surface. Therefore, to optimize the value of the LLZAO material in the composite cathode material, the structure, cycling stability, and rate performance of the NCM-LLZAO composite cathode material in ASSBs with oxide-based inorganic/organic-hybrid electrolytes were investigated using powder X-ray diffraction analysis, field-emission scanning electron microscopy, electrochemical impedance spectroscopy, and galvanostatic measurements.

Lithium-ion transport in inorganic active fillers used in PEO-based composite solid electrolyte sheets.

In this study, we evaluated the properties exhibited by a composite solid electrolyte (CSE) prepared via tailoring the particle size of an active filler, Li6.4La3Zr1.4Ta0.6O12 (LLZTO). The average particle size was reduced to 2.53 µm via ball milling and exhibited a specific surface area of 3.013 m2 g-1. Various CSEs were prepared by combining PEO and LLZTO/BM-LLZTO. The calculated lithium ionic conductivity of the BM-LLZTO CSE was 6.0 × 10-5 S cm-1, which was higher than that exhibited by the LLZTO CSE (4.6 × 10-5 S cm-1). This result was confirmed via 7Li nuclear magnetic resonance (NMR) analysis, during which lithium-ion transport pathways varied as a function of the particle size. NMR analysis showed that when BM-LLZTO was used, the migration of Li ions through the interface occurred at a fast rate owing to the small size of the constituent particles. During the Li/CSEs/Li symmetric cell experiment, the BM-LLZTO CSE exhibited lower overvoltage characteristics than the LLZTO CSE. A comparison of the characteristics exhibited by the LFP/CSEs/Li cells confirmed that the cells using BM-LLZTO exhibited high discharge capacity, rate performance, and cycling stability irrespective of the CSE thickness.

Facile synthesis of reduced graphene oxide by modified Hummer's method as anode material for Li-, Na- and K-ion secondary batteries.

Reduced graphene oxide (rGO) sheets were synthesized by a modified Hummer's method without additional reducing procedures, such as chemical and thermal treatment, by appropriate drying of graphite oxide under ambient atmosphere. The use of a moderate drying temperature (250°C) led to mesoporous characteristics with enhanced electrochemical activity, as confirmed by electron microscopy and N2 adsorption studies. The dimensions of the sheets ranged from nanometres to micrometres and these sheets were entangled with each other. These morphological features of rGO tend to facilitate the movement of guest ions larger than Li+. Impressive electrochemical properties were achieved with the rGO electrodes using various charge-transfer ions, such as Li+, Na+ and K+, along with high porosity. Notably, the feasibility of this system as the carbonaceous anode material for sodium battery systems is demonstrated. Furthermore, the results also suggest that the high-rate capability of the present rGO electrode can pave the way for improving the full cell characteristics, especially for preventing the potential drop in sodium-ion batteries and potassium-ion batteries, which are expected to replace the lithium-ion battery system.

Pyro-synthesis of functional nanocrystals.

Despite nanomaterials with unique properties playing a vital role in scientific and technological advancements of various fields including chemical and electrochemical applications, the scope for exploration of nano-scale applications is still wide open. The intimate correlation between material properties and synthesis in combination with the urgency to enhance the empirical understanding of nanomaterials demand the evolution of new strategies to promising materials. Herein we introduce a rapid pyro-synthesis that produces highly crystalline functional nanomaterials under reaction times of a few seconds in open-air conditions. The versatile technique may facilitate the development of a variety of nanomaterials and, in particular, carbon-coated metal phosphates with appreciable physico-chemical properties benefiting energy storage applications. The present strategy may present opportunities to develop "design rules" not only to produce nanomaterials for various applications but also to realize cost-effective and simple nanomaterial production beyond lab-scale limitations.

Low-temperature synthesis of LiFePO4 nanocrystals by solvothermal route.

LiFePO4 nanocrystals were synthesized at a very low temperature of 170°C using carbon nanoparticles by a solvothermal process in a polyol medium, namely diethylene glycol without any heat treatment as a post procedure. The powder X-ray diffraction pattern of the LiFePO4 was indexed well to a pure orthorhombic system of olivine structure (space group: Pnma) with no undesirable impurities. The LiFePO4 nanocrystals synthesized at low temperature exhibited mono-dispersed and carbon-mixed plate-type LiFePO4 nanoparticles with average length, width, and thickness of approximately 100 to 300 nm, 100 to 200 nm, and 50 nm, respectively. It also appeared to reveal considerably enhanced electrochemical properties when compared to those of pristine LiFePO4. These observed results clearly indicate the effect of carbon in improving the reactivity and synthesis of LiFePO4 nanoparticles at a significantly lower temperature.

The effects of Mo doping on 0.3Li[Li0.33Mn0.67]O2·0.7Li[Ni0.5Co0.2Mn0.3]O2 cathode material.

Mo doped Li excess transition metal oxides formulated as 0.3Li[Li(0.33)Mn(0.67)]O(2)·0.7Li[Ni(0.5-x)Co(0.2)Mn(0.3-x)Mo(2x)]O(2) were synthesized using the co-precipitation process. The effects of the substitution of Ni and Mn with Mo were investigated for the density of the states, the structure, cycling stability, rate performance and thermal stability by tools such as first principle calculations, synchrotron X-ray diffraction, field-emission SEM, solid state (7)Li MAS nuclear magnetic resonance (NMR), X-ray photoelectron spectroscopy (XPS), elemental mapping by scanning TEM (STEM), inductively coupled plasma atomic emission spectrometry (ICP-AES) and a differential scanning calorimeter (DSC). It was confirmed that high valence Mo(6+) doping of the Li-excess manganese-nickel-cobalt layered oxide in the transition metal enhanced the structural stability and electrochemical performance. This increase was due to strong Mo-O hybridization inducing weak Ni-O hybridization, which may reduce O(2) evolution, and metallic behavior resulting in a diminishing cell resistance.

Optimized Li4Ti5O12 nanoparticles by solvothermal route for Li-ion batteries.

Li4Ti5O12 (LTO) nanoparticles were successfully synthesized by solvothermal technique using cost-effective precursors in polyol medium and post-annealed at temperatures of 400, 500, and 600 degrees C. The XRD patterns of the samples were clearly indexed to the spinel shaped Li4Ti5O12 (space group, Fd-3 m). The particle size and morphology of samples were identified using field-emission SEM. The electrochemical performance of solvothermal samples revealed fairly high initial discharge/charge specific capacities in the range 230-235 and 170-190 mAh/g, at 1 C-rate, while that registered for the solid-state sample has been 160 and 150 mAh/g, respectively. Furthermore, among these samples, LTO annealed at 500 degrees C exhibited highly improved rate performances at C-rates as high as 30 and 60 C. This was attributed to the achievement of small particle sizes with high crystallinity in nano-scale dimensions and hence shorter diffusion paths combined with larger contact area at the electrode/electrolyte interface.

Synthesis of LiFePO4 nanoparticles by solvothermal process using various polyol media and their electrochemical properties.

Olivine structured LiFePO4 samples were synthesized by solvothermal process using various polyol media of ethylene glycol (EG), diethylene glycol (DEG), triethylene glycol (TEG), and tetraethylene glycol (TTEG) without any heating as a post procedure. The X-ray diffraction patterns of the samples prepared in EG and DEG showed the crystalline peaks with well-fitted to the positions on the basis of an olivine type structure without any impurities. In order to determine the unit cell parameters, synchrotron powder XRD patterns were fitted with whole-pattern profile matching method using FULLPROF program. The obtained samples exhibited well dispersed nanoplate morphologies excepting for the sample prepared in EG. The samples prepared in EG, DEG, TEG, and TTEG showed the reversible capacity of 118, 167, 90, and 105 mAh/g at current density of 0.1 mA/cm2, respectively. Among them, the samples reacted in DEG and TTEG showed good performances at high rate of 16C with high capacities retention.