Superconductivity Mechanism Controlled by Electric Dipole Correlation and Charge Correlation

It is strongly argued that high-temperature superconductors (HTSC) exhibit an antipolar phase state with long range order in normal and superconducting states. This antipolar phase is directly related to the onset of superconductivity in all high temperature superconductors and it is responsible for strong coupling and of two dimensionality aspect of HTSC, as it is described below.     

LiFePO4: From molten ingot to nanoparticles with high-rate performance in Li-ion batteries

LiFePO₄ (LFP) particles were obtained by grinding ingot synthesized in the molten state. This process, followed by jet milling, and then wet milling, provides a simple way to obtain powders with controlled particle size in the range from macroscopic to 25 nm. However, at this time, we find that these particles tend to agglomerate to form secondary particles of size ∼100 nm. The particles obtained by this process are characterized by X-ray diffraction (XRD). In situ and ex situ scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The effect of milling was also investigated by analysis of physical properties using infrared spectroscopy (FTIR) and magnetic measurements. The electrochemical performance was evaluated in cells containing Li/1 M LiPF₆ in EC:DEC (1:1)/C-LiFePO₄. After carbon coating, the LFP particles which are free of impurities, exhibit high-rate capability. Even with a limited amount of carbon (2 wt.%) appropriate for commercial batteries, the capacity is 157 mAh g⁻¹ at 0.1 C, 120 mAh g⁻¹ at 10 C, without capacity fading after 60 cycles.     

Investigations on TlBa2Ca2Cu3Ox superconducting thin films formation on LaAlO3 substrate

Investigations on pure superconducting phase TlBa₂Ca₂Cu₃O_x (Tl-1223) thin films formation, of about 100-125 nm in thickness, on (001) LaAlO₃ single crystal substrate, were made using radio-frequency sputtering deposition of Ba₂Ca₂Cu₃O_x precursor films and ex-situ thallination in sealed quartz tube. The precursor films were thallinated under different conditions of partial oxygen pressure, temperature, time and y thallium source content using unreacted pellets of composition Tl_yBa₂Ca₂Cu₃O_x. In all cases, strongly c-oriented multiphase films were obtained. A correlation between the Tl-1223 phase purity and the precursor film conditions of thallination is established. Temperature and time of thallination as well as the thallium source content and the partial pressure of oxygen play a key role in the quality of the obtained film. The films' onset temperature of the superconducting transition ranges between 90 and 103 K. It is shown that the best samples can be obtained from a dense precursor film and relatively medium thallination time.     

LiFePO4 and graphite electrodes with ionic liquids based on bis(fluorosulfonyl)imide (FSI) for Li-ion batteries

Ambient-temperature ionic liquids (IL) based on bis(fluorosulfonyl)imide (FSI) as anion and 1-ethyl-3-methyleimidazolium (EMI) or N-methyl-N-propylpyrrolidinium (Py13) as cations have been investigated with natural graphite anode and LiFePO₄ cathode in lithium cells. The electrochemical performance was compared to the conventional solvent EC/DEC with 1 M LiPF₆ or 1 M LiFSI. The ionic liquid showed lower first coulombic efficiency (CE) at 80% compared to EC–DEC at 93%. The impedance spectroscopy measurements showed higher resistance of the diffusion part and it increases in the following order: EC–DEC–LiFSI < EC–DEC–LiPF₆ < Py13(FSI)–LiFSIE = MI(FSI)–LiFSI. On the cathode side, the lower reversible capacity at 143 mAh g⁻¹ was obtained with Py13(FSI)–LiFSI; however, a comparable reversible capacity was found in EC–DEC and EMI(FSI)–LiFSI. The high viscosity of the ionic liquids suggests that different conditions such as vacuum and 60 °C are needed to improve impregnation of IL in the electrodes. With these conditions, the reversible capacity improved to 160 mAh g⁻¹ at C/24. The high-rate capability of LiFePO₄ was evaluated in polymer–IL and compared to the pure IL cells. The reversible capacity at C/10 decreased from 155 to only 126 mAh g⁻¹ when the polymer was present.     

Characterization of Na-based phosphate as electrode materials for electrochemical cells

We report the electrochemical properties of submicron-sized particles of NaFePO₄. Two materials have been studied and characterized by XRD, SEM, EDX, EIS and Raman experiments: the maricite phase synthesized by hydrothermal method and the olivine phase obtained from delithiation of LiFePO₄. NaFePO₄ materials have an electrochemical activity in Na cell using NaPF₆-EC-DEC electrolyte, but only in the heterosite phase, and the capacity is reduced already in the second cycle. The two-phase system at intermediate compositions has also been analyzed.     

High reversible capacities of graphite and SiO/graphite with solvent-free solid polymer electrolyte for lithium-ion batteries

The combination of graphite or silicon monoxide (SiO)/graphite = 1/1 mixture with a solvent-free solid polymer electrolyte (SPE) was fabricated using a new preparation process, involving precoating the electrode with vapor-grown carbon fiber (VGCF) and binders (polyvinyl difluoride: PVdF or polyimide: PI), followed by the overcoating of the SPE. The reversible capacity of [graphite | SPE | Li] and [SiO/graphite | SPE | Li] cells were >360 and >1000 mAh g⁻¹ with 78% and 77% for the 1st Coulombic efficiency, respectively. The reversible capacities were 75% at the 250th cycle for [graphite | SPE | Li] and 72% at the 100th cycle for [SiO/graphite | SPE | Li]. The electrode used was compatible with that of the conventional liquid electrolyte system, and the SPE film could be formed on the electrode by the continuous overcoating process, which will lead to a low-cost electrodes and low-cost battery production. The solid-state lithium-ion polymer battery (SSLiPB) developed in this study, which consisted of [LiFePO₄ | SPE | graphite], showed the reversible capacity of 128 mAh g⁻¹ (based on the LiFePO₄ capacity) with favorable cycle performance.     

Detection of Electrical Fault in Medium Voltage Installation Using Support Vector Machine and Artificial Neural Network

Russian Journal of Nondestructive Testing - Infrared thermography plays an important role in the inspection of electrical installations allowing to avoid failures and breakdowns. Condition...     

Alkaline aqueous electrolytes for secondary zinc–air batteries: an overview

New applications and emerging markets in electromobility and large‐scale stationary energy storage require the development of new electrochemical systems with higher energy density than current batteries. Rechargeable metal–air batteries, mainly lithium–air and zinc–air systems, are considered one of the most promising candidates. In contrast to lithium, zinc is abundant, inexpensive and its electrodeposition in aqueous electrolytes is relatively easy. Unfortunately, achieving a rechargeable zinc–air battery is still hindered by various technical problems related to the reversibility and lifetime of the electrodes. The most widely used electrolyte in zinc–air batteries has been the classical aqueous alkaline. In this context and with the main objective of providing a complete overview, we studied a wide number of articles starting from the beginning of the development of secondary zinc–air batteries (1970–1980s) to more recent works, with the aim of compiling all available information. It is essential to revise older papers to find relevant information that may get otherwise forgotten and not taken into account to develop new solutions. This information could also be applied in other storage systems based on zinc as nickel–zinc, zinc hybrid or zinc‐ion. Copyright © 2016 John Wiley & Sons, Ltd.     

LiFePO4 water-soluble binder electrode for Li-ion batteries

A new water-soluble elastomer from ZEON Corp. was evaluated as binder with LiFePO₄ cathode material in Li-ion batteries. The mechanical characteristic of this cathode was compared to that with PVdF-based cathode binder. The elastomer-based cathode shows high flexibility with good adhesion. The electrochemical performance was also evaluated and compared to PVdF-based cathodes at 25 and at 60 °C. A lower irreversible capacity loss was obtained with the elastomer-based cathode, however, aging at 60 °C shows a comparable cycle life to that observed with PVdF-based cathodes. The LiFePO₄–WSB at high rate shows a good performance with 120 mAh g⁻¹ at 10C rate at 60 °C.     

Enabling High-Performance NASICON-Based Solid-State Lithium Metal Batteries Towards Practical Conditions

Solid-state lithium metal batteries (SSLMBs) are promising next-generation high-energy rechargeable batteries. However, the practical energy densities of the reported SSLMBs have been significantly overstated due to the use of thick solid-state electrolytes, thick lithium (Li) anodes, and thin cathodes. Here, a high-performance NASICON-based SSLMB using a thin (60 µm) Li_1.5Al_0.5Ge_1.5(PO₄)₃ (LAGP) electrolyte, ultrathin (36 µm) Li metal, and high-loading (8 mg cm⁻²) LiFePO₄ (LFP) cathode is reported. The thin and dense LAGP electrolyte prepared by hot-pressing exhibits a high Li ionic conductivity of 1 × 10⁻³ S cm⁻¹ at 80 °C. The assembled SSLMB can thus deliver an increased areal capacity of ≈1 mAh cm⁻² at C/5 with a high capacity retention of ≈96% after 50 cycles under 80 °C. Furthermore, it is revealed by synchrotron X-ray absorption spectroscopy and in situ high-energy X-ray diffraction that the side reactions between LAGP electrolyte and LFP cathode are significantly suppressed, while rational surface protection is required for Ni-rich layered cathodes. This study provides valuable insights and guidelines for the development of high-energy SSLMBs towards practical conditions.