Academia.edu no longer supports Internet Explorer.
To browse Academia.edu and the wider internet faster and more securely, please take a few seconds to upgrade your browser.
…
8 pages
1 file
AI-generated Abstract
Modeling and simulations are critical for the design, optimization, and operation of lithium-ion batteries. These techniques facilitate analysis of design parameters and operating conditions which leads to better understanding and performance of batteries in consumer electronics and other applications. The paper highlights the evolution of mathematical models since the 1990s and illustrates the importance of these models in identifying limitations, optimizing designs, and ensuring safety across various operational scenarios.
Computers & Chemical Engineering, 2011
The lithium-ion battery is an ideal candidate for a wide variety of applications due to its high energy/power density and operating voltage. Some limitations of existing lithium-ion battery technology include underutilization, stress-induced material damage, capacity fade, and the potential for thermal runaway. This paper reviews efforts in the modeling and simulation of lithium-ion batteries and their use in the design of better batteries. Likely future directions in battery modeling and design including promising research opportunities are outlined.
Sustainability, 2021
The growing demand for electrical energy and the impact of global warming leads to a paradigm shift in the power sector. This has led to the increased usage of renewable energy sources. Due to the intermittent nature of the renewable sources of energy, devices capable of storing electrical energy are required to increase its reliability. The most common means of storing electrical energy is battery systems. Battery usage is increasing in the modern days, since all mobile systems such as electric vehicles, smart phones, laptops, etc., rely on the energy stored within the device to operate. The increased penetration rate of the battery system requires accurate modelling of charging profiles to optimise performance. This paper presents an extensive study of various battery models such as electrochemical models, mathematical models, circuit-oriented models and combined models for different types of batteries. It also discusses the advantages and drawbacks of these types of modelling. Wi...
Energies
Battery models have gained great importance in recent years, thanks to the increasingly massive penetration of electric vehicles in the transport market. Accurate battery models are needed to evaluate battery performances and design an efficient battery management system. Different modeling approaches are available in literature, each one with its own advantages and disadvantages. In general, more complex models give accurate results, at the cost of higher computational efforts and time-consuming and costly laboratory testing for parametrization. For these reasons, for early stage evaluation and design of battery management systems, models with simple parameter identification procedures are the most appropriate and feasible solutions. In this article, three different battery modeling approaches are considered, and their parameters’ identification are described. Two of the chosen models require no laboratory tests for parametrization, and most of the information are derived from the ...
IEEE Transactions on Energy Conversion, 2006
To draw reliable conclusions about the internal state of a lithium-ion battery or about ageing processes using physico-chemical models, the determination of the correct set of input parameters is crucial. In the first part of this publication, the complete set of material parameters for model parameterisation has been determined by experiments for a 7.5 Ah cell produced by Kokam. In this part of the publication, the measured set of parameters is incorporated into a physico-chemical model. Model results are compared to validation test results conducted on laboratory-made coin cells produced with materials obtained from the Kokam cell. The model is also compared to laboratory-made coin half cell experiments where anode or cathode materials obtained from the Kokam cell have been tested against metallic lithium as counter electrode, to prove the behaviour of the single electrodes. Finally, the model is scaled to reproduce the original Kokam cell and model results are validated by comparison with measurement results. The influence of temperature is considered as well. It is discussed, to which extent material parameters obtained by experimental investigation of laboratory coin cells can be transferred to commercial cells of the same material. The validity of physico-chemical models to describe cells is shown.
A first-principles-based charge-discharge model was developed to simulate the capacity fade of Li-ion batteries. The model is based on the loss of active lithium ions due to solvent reduction reaction and on the rise of the anode film resistance. The effect of parameters such as exchange current density, depth of discharge DOD, end of charge voltage, film resistance, and the overvoltage of parasitic reaction were studied quantitatively. The model controls the required DOD by controlling the discharge time and estimates the end of discharge voltages as a function of cycle number. Accelerated cycle life testing and developing correlations based on this data are critical for the capacity fade evaluation of batteries. 1-3 Darling and Newman 4 made a first attempt to model the parasitic reactions in lithium-ion batteries by incorporating a solvent oxidation into a lithium-ion battery model. Spotnitz 5 developed polynomial expressions for estimation of irreversible and reversible capacity loss due to solid electrolyte interphace SEI film growth and dissolution in lithium-ion batteries. Ramadass et al. 6 developed a capacity fade prediction model for Li-ion cells based on a semi-empirical approach. Recently, Christensen and Newman 7 simulated the influence of the anode film resistance on the charge/discharge performance of a lithium-ion battery. In this model the loss of reversible lithium ions and increase in the anode film resistance were incorporated into the first-principles model developed by Doyle et al. 8 Process parameters such as charge rate CR, the depth of discharge DOD, end-of-charge voltage EOCV, and the discharge rate DR which influence the capacity fade 9 were not considered in the above-mentioned models. We developed a first-principles-based model to simulate the capacity fade of Li-ion batteries in which incorporation of a continuous occurrence of the solvent reduction reaction during constant current and constant voltage CC-CV charging explains the capacity fade of the battery. 10 Initially the model estimates the capacity fade parameters as a function of cycle number. Next it is necessary to run the lithium-ion intercalation model with the updated parameters to estimate the performance of the battery at a specific cycle number. However, to run both models takes a long computational time. Also, the model does not consider the discharge process, which leads to inaccurate estimation of the total reaction time for the parasitic reaction. In this paper, a charge-discharge capacity fade model was developed based on the loss of active lithium ions due to solvent reduction reaction. The rise of the surface film resistance at the anode due to the parasitic reaction occurring was also considered in the model. The model considers process parameters such as: CR, DOD, EOCV, and the DR. It controls the required DOD by controlling the discharge time and estimates the discharge voltage as a function of cycle number. To decrease the computational time, the transport of lithium in the liquid phase was neglected. It takes only 10 h using a computer with 2.0 GHz CPU and 512 Mb RAM to run the model and to estimate the capacity fade and the charge-discharge performance of a battery cycled up to 2000 times. Model Development The simulations were carried out based on the experimental data obtained for a pouch lithium-ion cell 2.187 Ah, which consists of Li x CoO 2 positive electrode and mesocarbon microbead MCMB negative electrode. The charge-discharge simulations were performed by using a direct charge current of 0.334 A to a specified EOCV of 4.0 or 4.2 V. Next, the voltage was held constant until the charge current decreased to 50 mA. Subsequently, the battery was discharged under a direct current of 0.835 A to a specified DOD of 0.4 or 0.6. There was no rest time between charging and discharging. For simulation of the capacity check, the battery was initially discharged using a discharge current of 0.835 A to 3.0 V. Next, the battery was charged by applying a conventional CC-CV protocol 0.334 A to 4.2 V with a 50 mA cutoff current. The fully charged battery was discharged for second time to 3.0 V. The value of discharge capacity estimated in the second discharge process was used for capacity fade analysis. Both charge-discharge and the capacity check simulations terminate when the battery reaches a voltage lower than 3.0 V. As shown in Fig. 1, during discharge, the lithium ions deinterca-late from the negative electrode and intercalate into the positive electrode. Inside the porous electrode, the intercalation/ deintercalation processes take place at the electrode/electrolyte interface. A rigorous model based on porous electrode theory, concentrated solution theory, Ohm's law, and intercalation/deintercalation kinetics was developed previously which simulates the galvanostatic charge/discharge behavior of a Li-ion rechargeable battery. 8 In the model suggested in this paper, the variation of Li concentration in the liquid phase along the current path was neglected because low-to-medium charge/discharge currents were used in the simulations. The variation in the solid phase potential at the anode or at the cathode is negligible because of good conductivity of the electrode materials. It was also assumed that the active electrode materials are made from uniform spherical particles with a radius of R i and that the diffusion is the only mechanism of lithium transport inside the particles. The direction normal to the surface of the particles was taken to be the r-direction. The model equation that describes the diffusion of lithium in the solid phase is given by Fick's 2nd law
Interface magazine, 2012
Advances in Chemical Engineering and Science, 2014
Fundamental physical and (electro) chemical principles of rechargeable battery operation form the basis of the electronic network models developed for Nickel-based aqueous battery systems, including Nickel Metal Hydride (NiMH), and non-aqueous battery systems, such as the well-known Li-ion. Refined equivalent network circuits for both systems represent the main contribution of this paper. These electronic network models describe the behavior of batteries during normal operation and during over (dis) charging in the case of the aqueous battery systems. This makes it possible to visualize the various reaction pathways, including convention and pulse (dis) charge behavior and for example, the self-discharge performance.
International Journal of Energy Research, 2016
We describe an advanced lithium-ion battery model for system-level analyses such as electric vehicle fleet simulation or distributed energy storage applications. The model combines an empirical multi-parameter model and an artificial neural network with particular emphasis on thermal effects such as battery internal heating. The model is fast and can accurately describe constant current charging and discharging of a battery cell at a variety of ambient temperatures. Comparison to a commonly used linear kilowatt-hour counter battery model indicates that a linear model overestimates the usable capacity of a battery at low temperatures. We highlight the importance of including internal heating in a battery model at low temperatures, as more capacity is available when internal heating is taken into account.
Journal of The Electrochemical Society, 2015
To draw reliable conclusions about the internal state of a lithium-ion battery or about ageing processes using physico-chemical models, the determination of the correct set of input parameters is crucial. In the first part of this publication, the complete set of material parameters for model parameterization has been determined by experiments for a 7.5 Ah cell produced by Kokam. In this part of the publication, the measured set of parameters is incorporated into a physico-chemical model. Model results are compared to validation test results conducted on the Kokam cell. The influence of current rate and temperature is considered as well as a comparison with pulse tests is shown. It is discussed to which extent material parameters obtained by experimental investigation of laboratory coin cells can be transferred to commercial cells of the same material. The validity of physico-chemical models to describe cells is shown.
The Collapse of Democracies and the Need for a New Aristocracy -- stand Oct. 1, 2024, 2024
Flight MH17, Ukraine and the new Cold War, 2018
SÍNTESIS. Revista de Filosofía, 2019
Psicologia da Educação, 2023
musings: food feminism fermentation, 2021
… , Baltimore, MD, USA, 2004
Journal of the Royal Asiatic Society, 2019
Journal of The Royal Society Interface
The Halcyon and the Anthropocene
Molecular and Cellular Neuroscience, 2004
International journal of Nursing Didactics, 2015
Revista Argentina de Educación Superior, 2021
European Heart Journal, 2018