Historians in Flux: The Concept, Task and Challenge of ego-histoire

No abstrac

Historians in Flux: The Concept, Task and Challenge of ego-histoire

No abstrac

A note on the integral equation for the Wilson loop in N = 2 D=4 superconformal Yang-Mills theory

We propose an alternative method to study the saddle point equation in the strong coupling limit for the Wilson loop in $\mathcal{N}=2$ D=4 super Yang-Mills with an SU(N) gauge group and 2N hypermultiplets. This method is based on an approximation of the integral equation kernel which allows to solve the simplified problem exactly. To determine the accuracy of this approximation, we compare our results to those obtained recently by Passerini and Zarembo. Although less precise, this simpler approach provides an explicit expression for the density of eigenvalues that is used to derive the planar free energy.Comment: 12 pages, v2: section 2.5 (Free Energy) amended and reference added, to appear in J. Phys.

High temperature stable separator for lithium batteries based on SiO² and hydroxypropyl guar gum

A novel membrane based on silicon dioxide (SiO$_{2}$) and hydroxypropyl guar gum (HPG) as binder is presented and tested as a separator for lithium-ion batteries. The separator is made with renewable and low cost materials and an environmentally friendly manufacturing processing using only water as solvent. The separator offers superior wettability and high electrolyte uptake due to the optimized porosity and the good affinity of SiO$_{2}$ and guar gum microstructure towards organic liquid electrolytes. Additionally, the separator shows high thermal stability and no dimensional-shrinkage at high temperatures due to the use of the ceramic filler and the thermally stable natural polymer. The electrochemical tests show the good electrochemical stability of the separator in a wide range of potential, as well as its outstanding cycle performance

Metal–organic framework derived Fe7S8 nanoparticles embedded in heteroatom-doped carbon with Lithium and Sodium storage capability

Iron sulfides are promising materials for lithium- and sodium-ion batteries owing to their high theoretical capacity and widespread abundance. Herein, the performance of an iron sulfide-carbon composite, synthesized from a Fe-based metal–organic framework (Fe-MIL-88NH2) is reported. The material is composed of ultrafine Fe7S8 nanoparticles (<10 nm in diameter) embedded in a heteroatom (N, S, and O)-doped carbonaceous framework (Fe7S8@HD-C), and is obtained via a simple and efficient one-step sulfidation process. The Fe7S8@HD-C composite, investigated in diethylene glycol dimethyl ether-based electrolytes as anode material for lithium and sodium batteries, shows high reversible capacities (930 mAh g−1 for lithium and 675 mAh g−1 for sodium at 0.1 A g−1). In situ X-ray diffraction reveals an insertion reaction to occur in the first lithiation and sodiation steps, followed by conversion reactions. The composite electrodes show rather promising long-term cycling stability and rate capability for sodium storage in glyme electrolyte, while an improved rate capacity and long-term cycling stability (800 mAh g−1 after 300 cycles at 1 A g−1) for lithium can be achieved using conventional carbonates

Electrolytes and Interphases in Sodium-Based Rechargeable Batteries: Recent Advances and Perspectives

For sodium (Na)-rechargeable batteries to compete, and go beyond the currently prevailing Li-ion technologies, mastering the chemistry and accompanying phenomena is of supreme importance. Among the crucial components of the battery system, the electrolyte, which bridges the highly polarized positive and negative electrode materials, is arguably the most critical and indispensable of all. The electrolyte dictates the interfacial chemistry of the battery and the overall performance, having an influence over the practical capacity, rate capability (power), chemical/thermal stress (safety), and lifetime. In-depth knowledge of electrolyte properties provides invaluable information to improve the design, assembly, and operation of the battery. Thus, the full-scale appraisal of both tailored electrolytes and the concomitant interphases generated at the electrodes need to be prioritized. The deployment of large-format Na-based rechargeable batteries also necessitates systematic evaluation and detailed appraisal of the safety-related hazards of Na-based batteries. Hence, this review presents a comprehensive account of the progress, status, and prospect of various Na+-ion electrolytes, including solvents, salts and additives, their interphases and potential hazards

Reinforcing the Electrode/Electrolyte Interphases of Lithium Metal Batteries Employing Locally Concentrated Ionic Liquid Electrolytes

Lithium metal batteries (LMBs) with nickel-rich cathodes are promising candidates for next-generation high-energy-density batteries, but the lack of sufficiently protective electrode/electrolyte interphases (EEIs) limits their cyclability. Herein, trifluoromethoxybenzene is proposed as a cosolvent for locally concentrated ionic liquid electrolytes (LCILEs) to reinforce the EEIs. With a comparative study of a neat ionic liquid electrolyte (ILE) and three LCILEs employing fluorobenzene, trifluoromethylbenzene, or trifluoromethoxybenzene as cosolvents, it is revealed that the fluorinated groups tethered to the benzene ring of the cosolvents not only affect the electrolytes' ionic conductivity and fluidity, but also the EEIs' composition via adjusting the contribution of the 1-ethyl-3-methylimidazolium cation (Emim+) and bis(fluorosulfonyl)imide anion. Trifluoromethoxybenzene, as the optimal cosolvent, leads to a stable cycling of LMBs employing 5 mAh cm-2 lithium metal anodes (LMAs), 21 mg cm-2 LiNi0.8Co0.15Al0.05 (NCA) cathodes, and 4.2 mu L mAh-1 electrolytes for 150 cycles with a remarkable capacity retention of 71%, thanks to a solid electrolyte interphase rich in inorganic species on LMAs and, particularly, a uniform cathode/electrolyte interphase rich in Emim+-derived species on NCA cathodes. By contrast, the capacity retention under the same condition is only 16%, 46%, and 18% for the neat ILE and the LCILEs based on fluorobenzene and benzotrifluoride, respectively.A locally concentrated ionic liquid electrolyte based on trifluoromethoxybenzene cosolvent is proposed for lithium metal batteries with nickel-rich cathodes, through a comparative study of three fluorinated aromatic cosolvents. The generated solid electrolyte interphase rich in inorganic species on anodes and, particularly, a uniform cathode/electrolyte interphase rich in organic cation-derived species on cathodes enable stable cycling of Li/LiNi0.8Co0.15Al0.05O2 cells.imag

Management of imatinib-resistant CML patients

Imatinib has had marked impact on outcomes in chronic myelogenous leukemia (CML) patients for all stages of the disease and is endorsed by international treatment guidelines as the first line option. Although imatinib is highly effective and well tolerated, the development of resistance represents a clinical challenge. Since the most frequently identified mechanism of acquired imatinib resistance is bcr-abl kinase domain point mutations, periodic hematologic, cytogenetic, and molecular monitoring is critical throughout imatinib therapy. Once cytogenetic remission is achieved, residual disease can be monitored by bcr-abl transcript levels as assayed by reverse transcription polymerase chain reaction (RT-PCR). Detection of bcr-abl mutants prior to and during imatinib therapy can aid in risk stratification as well as in determining therapeutic strategies. Thus, mutation screening is indicated in patients lacking or losing hematologic response. Moreover, search for mutations should also be performed when a 3-log reduction of bcr-abl transcripts is not achieved or there is a reproducible increase of transcript levels. In patients harboring mutations which confer imatinib resistance, novel second line tyrosine kinase inhibitors have demonstrated encouraging efficacy with low toxicity. Only the T315I bcr-abl mutant has proved totally resistant to all clinically available bcr-abl inhibitors. Strategies to further increase the rates of complete molecular remissions represent the next frontier in the targeted therapy of CML patients

High-capacity Li4Ti5O12-C thick ceramic electrodes manufactured by powder injection moulding

Lithium-ion batteries are the most efficient electrochemical energy storage devices. However, there is still room for improvement in terms of safety and energy density, presently limited by conventional tape-casting electrode processing. In this study, a blend of the anodic material Li$_{4}$Ti$_{5}$O$_{12}$ with 2 wt% carbon black has been processed through powder injection moulding (PIM) yielding, after subsequent debinding and sintering processes, to ultra-thick (>500 µm) ceramic binder-free electrodes. The mixture of Li$_{4}$Ti$_{5}$O$_{12}$ with the thermoplastic binder composed of polypropylene, paraffin wax, and stearic acid is investigated to identify a rheologically suitable feedstock for the PIM process. The resulting disk-type green parts contain 50 vol% of ceramic powder. After removing the binder with solvents and subsequent thermal treatment, the parts are sintered at 900 °C, aiming for a relatively high porosity, i.e., 25.7%. The resulting electrodes show very high areal and volumetric capacities up to 26.0 mA·h·cm−2 and 403 mA·h·cm−3 at C/24, respectively, in a half-cell against lithium metal

Ionic Liquid Electrolytes for Safer Lithium Batteries – I. Investigation around Optimal Formulation

In this paper we report on the investigation of ionic liquid-based electrolytes with enhanced characteristics. In particular, we have studied ternary mixtures based on the lithium bis(trifluoromethanesulfonyl)imide (LiTFSI) salt and two ionic liquids sharing the same cation (N-methyl-N-propyl pyrrolidinium, PYR13), but different anions, bis(trifluoromethanesulfonyl)imide (TFSI) and bis(fluorosulfonyl)imide (FSI). The LiTFSI-PYR13TFSI-PYR13FSI mixtures, found to be ionically dissociated, exhibit better ion transport properties (about 10−3 S cm−1 at −20°C) with respect to similar ionic liquid electrolytes till reported in literature. An electrochemical stability window of 5 V is observed in carbon working electrodes. Preliminary battery tests confirm the good performance of these ternary electrolytes with high-voltage NMC cathodes and graphite anodes