25 research outputs found
Comparative study of the implementation of tin and titanium oxide nanoparticles as electrodes materials in Li-ion batteries
Transition metal oxides potentially present higher specific capacities than the current anodes based on carbon, providing an increasing energy density as compared to commercial Li-ion batteries. However, many parameters could influence the performance of the batteries, which depend on the processing of the electrode materials leading to different surface properties, sizes or crystalline phases. In this work a comparative study of tin and titanium oxide nanoparticles synthesized by different methods, undoped or Li doped, used as single components or in mixed ratio, or alternatively forming a composite with graphene oxide have been tested demonstrating an enhancement in capacity with Li doping and better cyclability for mixed phases and composite anodes
Fluor und Lithium: Ideale Partner fĂŒr Elektrolyte in wiederaufladbaren Hochleistungsbatterien
Measurement of transference numbers for lithium ion electrolytes via four different methods, a comparative study
Salt Diffusion Coefficients, Concentration Dependence of Cell Potentials, and Transference Numbers of Lithium Difluoromono(oxalato)borate-Based Solutions
Several properties of the electrolyte solution lithium difluoromono(oxalato)borate (LiDFOB) in ethylene carbonate diethylcarbonate (EC/DEC (3:7 mass ratio)) are given, including transference numbers, diffusion coefficients, concentration dependence of cell potentials, and the Haven ratio. The concentration range of the salt covers 0.1 mol·kgâ1 to 1.0 mol·kgâ1. In comparison to the standard salt LiPF6 currently in use in lithium ion cells LiDFOB has higher transference numbers. However, the Haven ratio related to ion pair formation in an electrolyte indicates a high amount of aggregates in concentrated LiDFOB/EC/DEC (3:7) electrolytes
The truth about the 1st cycle Coulombic efficiency of LiNi Co Mn O (NCM) cathodes
The 1st cycle Coulombic efficiency (CE) of LiNi1/3Co1/3Mn1/3O2 (NCM) at 4.6 V vs. Li/Li+ has been extensively investigated in NCM/Li half cells. It could be proven that the major part of the observed overall specific capacity loss (in total 36.3 mA h gâ1) is reversible and induced by kinetic limitations, namely an impeded lithiation reaction during discharge. A measure facilitating the lithiation reaction, i.e. a constant potential (CP) step at the discharge cut-off potential, results in an increase in specific discharge capacity of 22.1 mA h gâ1. This capacity increase during the CP step could be proven as a relithiation process by Li+ content determination in NCM via an ICP-OES measurement. In addition, a specific capacity loss of approx. 4.2 mA h gâ1 could be determined as an intrinsic reaction to the NCM cathode material at room temperature (RT). In total, less than 10.0 mA h gâ1 (=28% of the overall capacity loss) can be attributed to irreversible reactions, mainly to irreversible structural changes of NCM. Thus, the impact of parasitic reactions, such as oxidative electrolyte decomposition, on the irreversible capacity is negligible and could also be proven by on-line MS. As a consequence, the determination of the amount of extracted Li+ (âLi+ extraction ratioâ) so far has been incorrect and must be calculated by the charge capacity (=delithiation amount) divided by the theoretical capacity. In a NCM/graphite full cell the relithiation amount during the constant voltage (CV) step is smaller than in the half cell, due to irreversible Li+ loss at graphite
Electrolytes for lithium and lithium ion batteries: From synthesis of novel lithium borates and ionic liquids to development of novel measurement methods
Electrolyte Additives Improving the Cycling Stability and Reducing Degradation of LIB Cathodes at High Voltage & Some Simple Experiments Clarifying âCapacity Lossesâ at the Cathode
Electrolyte Additives Improving the Cycling Stability and Reducing Degradation of LIB Cathodes at High Voltage & Some Simple Experiments Clarifying âCapacity Lossesâ at the Cathode
The goal of this work is the design of integrated circuits in order to efficiently draw images on a computer screen display. Ten years ago, we designed an LSI integrated circuit, which managed a screen buffer, and fastly drew vectors and characters, in an architecture of "graphic terminal". Then, we tried to optimize such an architecture, and to adapt it to a "workstation" environment. We are now convinced that the best way to do it is not to wire specialized algorithms, but to define fast generalized computing functions. In order to explain our evolution, we describe successive experimentations, preceded by a short history of display architectures.La motivation de ce travail est la réalisation de circuits permettant d'afficher rapidement des images sur un écran d'ordinateur. Voici dix ans, nous avons proposé un circuit LSI, prenant en charge la gestion d'une mémoire d'image et l'écriture rapide de segments de droite et de caractÚres, dans une optique de "terminal graphique". Nous avons ensuite cherché à augmenter les performances de cette architecture et à l'adapter à l'environnement "station de travail". Nous sommes aujourd'hui convaincu que la solution ne passe pas par des circuits spécialisés, mais par la définition d'opérateurs généraux de calcul trÚs puissants. Pour expliquer cet itinéraire, nous décrivons une suite d'expérimentations réalisées, précédée par une histoire des architectures de visualisation