48 research outputs found

    TS2PACK: A Two-Level Tabu Search for the Three-dimensional Bin Packing Problem

    Get PDF
    Three-dimensional orthogonal bin packing is a problem NP-hard in the strong sense where a set of boxes must be orthogonally packed into the minimum number of three-dimensional bins. We present a two-level tabu search for this problem. The first-level aims to reduce the number of bins. The second optimizes the packing of the bins. This latter procedure is based on the Interval Graph representation of the packing, proposed by Fekete and Schepers, which reduces the size of the search space. We also introduce a general method to increase the size of the associated neighborhoods, and thus the quality of the search, without increasing the overall complexity of the algorithm. Extensive computational results on benchmark problem instances show the effectiveness of the proposed approach, obtaining better results compared to the existing one

    Métaheuristiques de recherche avec tabous pour le problÚme de synthÚse de réseau multiproduits avec capacités

    Get PDF
    ThÚse numérisée par la Direction des bibliothÚques de l'Université de Montréal

    Degradation Phenomena in Silicon/Graphite Electrodes with Varying Silicon Content

    Get PDF
    The degradation phenomena of Silicon/Graphite electrodes and the effect of FEC as electrolyte additive was investigated through galvanostatic cycling, XPS analyses and SEM cross section analyses. To understand the direct influence of silicon on the electrode degradation, the silicon amount was varied between 0%–30%. By evaluating the cycling performance and the accumulated capacity loss of the different Si/Gr electrodes (cycled with and without 10 vol-% of FEC), we see that the capacity decay can be distinguished into two phenomena, where one is independent of the Si/Gr ratio while the other one depends on the Si content. As expected, adding FEC improves the cell performance and minimizes the capacity decay. Combing our XPS data and SEM cross section analyses on cycled electrodes, this improvement stems from a thin and flexible SEI including poly(vinyl carbonate) that helps maintaining the overall electrode integrity as we observe less electrode fractures and less pronounced thickness increase. Si/Gr electrodes with 10 and 20% Si content showed very similar accumulated irreversible capacity losses over 100 cycles indicating that with 10 % FEC as electrolyte additive, also higher Si contents could be feasible for future high energy density anodes

    Origin of the catalytic activity at graphite electrodes in vanadium flow batteries

    Get PDF
    For many electrochemical devices that use carbon-based materials such as electrolyzers, supercapacitors, and batteries, oxygen functional groups (OFGs) are considered essential to facilitate electron transfer. Researchers implement surface-active OFGs to improve the electrocatalytic properties of graphite felt electrodes in vanadium flow batteries. Herein, we show that graphitic defects and not OFGs are responsible for lowering the activation energy barrier and thus enhance the charge transfer properties. This is proven by a thermal deoxygenation procedure, in which specific OFGs are removed before electrochemical cycling. The electronic and microstructural changes associated with deoxygenation are studied by quasi in situ X-ray photoelectron and Raman spectroscopy. The removal of oxygen groups at basal and edge planes improves the activity by introducing new active edge sites and carbon vacancies. OFGs hinder the charge transfer at the graphite–electrolyte interface. This is further proven by modifying the sp2 plane of graphite felt electrodes with oxygen-containing pyrene derivatives. The electrochemical evolution of OFGs and graphitic defects are studied during polarization and long-term cycling conditions. The hypothesis of increased activity caused by OFGs was refuted and hydrogenated graphitic edge sites were identified as the true reason for this increase

    Enhancing the Stability of LiNio.5_{o.5}0Mn1.5_{1.5}O4_{4} by Coating with LiNbO3_{3} Solid-State Electrolyte: Novel Chemically Activated Coating Process versus Sol-Gel Method

    Get PDF
    LiNbO3_{3}-coated LiNi0.5_{0.5}Mn1.5_{1.5}O4_{4} spinel was fabricated by two methods: using hydrogen-peroxide as activating agent and sol-gel method. The structure of the obtained cathode materials was investigated using a scanning electron microscope (SEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and the electrochemical properties of the prepared cathodes were probed by charge-discharge studies. The morphology of the coating material on the surface and the degree of coverage of the coated particles were investigated by SEM, which showed that the surface of LiNi0.5_{0.5}Mn1.5_{1.5}O4_{4} particles is uniformly encapsulated by lithium innovate coating. The influence of the LiNbO3 coating layer on the spinel’s properties was explored, including its effect on the crystal structure and electrochemical performance. XRD studies of the obtained coated active materials revealed very small expansion or contraction of the unit cell. From the capacity retention tests a significant improvement of the electrochemical properties resulted when a novel chemically activated coating process was used. Poorer results, however, were obtained using the sol-gel method. The results also revealed that the coated materials by the new method exhibit enhanced reversibility and stability compared to the pristine and reference ones. It was shown that the morphology of the coating material and possible improvement of communication between the substrates play an important role

    Interphase formation with carboxylic acids as slurry additives for Si electrodes in Li-ion batteries. Part 2: a photoelectron spectroscopy study

    Get PDF
    The mass loading of Si–graphite electrodes is often considered as a parameter of secondary importance when testing their electrochemical performance. However, if a sacrificial additive is present in the electrolyte to improve the electrochemical performance, the electrode loading becomes the battery cycle-life-determining factor. The correlation between mass-loading, electrolyte additive, and binder type was investigated by analyzing the cycling behavior of Si–graphite electrodes, prepared with water-based binders, with mass loading ranging from 3 to 9.5 mg cm-2 and cycled with FEC electrolyte additive, while keeping electrolyte amount constant. A lower loading was obtained by keeping slurry preparation steps unchanged from binder to binder and resulted in a longer lifetime for some of the binders. When the final loading was kept constant instead, the performance became independent of the binder used. Because such results can lead to the misinterpretation of the influence of electrode components on the cycling stability (and to a preference of one binder over another in our case), we propose that a comparison of long-term electrochemical performance data of Si–graphite electrodes needs to be always collected by using the same mass-loading with the constant electrolyte and additive
    corecore