9 research outputs found
Thermal Model for a Li-Ion Cell
A thermal model for a lithium-ion cell is presented and used to predict discharge performance at different operating temperatures. The results from the simulations are compared to experimental data obtained from lithium-ion pouch cells. The model includes a set of parameters (and their concentration and temperature dependencies) that has been obtained for a lithium-ion cell composed of a mesocarbon microbead anode, LiCoO2 cathode in 1 M LiPF6 salt, in a mixture of ethylene carbonate, propylene carbonate, ethyl-methyl carbonate, and diethyl carbonate electrolyte. The parameter set was obtained by comparing the model predictions to the experimental discharge profiles obtained at various temperatures and rates. The concentration and temperature dependence of the extracted parameters were correlated through empirical expressions. Also, the effect of including the thermal dependence of various parameters in the model on the simulated discharge profiles is discussed
Effect of Porosity on the Capacity Fade of a Lithium-Ion Battery: Theory
A mathematical model is presented to predict the performance of a lithium-ion battery. It includes the changes in the porosity of the material due to the reversible intercalation processes and the irreversible parasitic reaction. The model was also extended to predict the capacity fade in a lithium-ion battery based on the unwanted parasitic reaction that consumes Li+ along with the changes in the porosities of the electrodes with cycling due to the continuous parasitic side reaction. The model can be used to predict the drop in the voltage profile, change in the state of charge, and the effects of charge and discharge rates during cycling
A Mathematical Model for a Lithium-Ion Battery/Electrochemical Capacitor Hybrid System
A one-dimensional model for predicting the performance of a battery/electrochemical capacitor-hybrid system has been developed. Simulation results are presented for a LiCoO2|LiPF6 ethylene carbonate/dimethyl carbonate|carbon battery system and a Maxwell PC 10F carbon double-layer electrochemical capacitor. The current shared between the battery and the electrochemical capacitor at very short times depends on the ohmic resistances of the battery and the capacitor. As the discharge proceeds, the operating conditions such as frequency, duty ratio, and peak pulse discharge current control the current shared among parallel circuits. These parameters also determine the extent of the run time increase of the hybrid system as compared to the battery system. The inclusion of a number of identical series/parallel capacitors is considered in the present model by introducing the parameter, capacitor configuration index. Ragone plots are simulated for a battery-alone and a hybrid system. A substantial improvement in the available energy density is observed while operating hybrid systems under high power densities. Finally, a general optimization approach is presented
Analytical Expression for the Impedance Response of an Insertion Electrode Cell
An analytical expression for the impedance response of an insertion cathode/separator/foil anode cell sandwich is presented. The analytical expression includes the impedance contributions from interfacial kinetics, double-layer adsorption, and solution-phase and solid-phase diffusion processes. The validity of the analytical solution is ascertained by comparison with the numerical solution obtained for a LiCoO2 /polypropylene/lithium metal cell. The flexibility of the analytical solution is utilized to analyze various limiting conditions. An expression to estimate solid-phase diffusion coefficient of insertion species in a porous electrode influenced by the solution-phase diffusion process is also derive
Theoretical Analysis of Stresses in a Lithium Ion Cell
A mathematical model to simulate the generation of mechanical stress during the discharge process in a dual porous insertion electrode cell sandwich comprised of lithium cobalt oxide and carbon is presented. The model attributes stress buildup within intercalation electrodes to two different aspects: changes in the lattice volume due to intercalation and phase transformation during the charge/discharge process. The model is used to predict the influence of cell design parameters such as thickness, porosity, and particle size of the electrodes on the magnitude of stress generation. The model developed in this study can be used to understand the mechanical degradation in a porous electrode during an intercalation/deintercalation process, and the use of this model results in an improved design for battery electrodes that are mechanically durable over an extended period of operation
Analytical Expression for the Impedance Response for a Lithium-Ion Cell
An analytical expression to predict the impedance response of a dual insertion electrode cell (insertion electrodes separated by an ionically conducting membrane) is presented. The expression accounts for the reaction kinetics and double-layer adsorption processes at the electrode-electrolyte interface, transport of electroactive species in the electrolyte phase, and insertion of species in the solid phase of the insertion electrodes. The accuracy of the analytical expression is validated by comparing the impedance response predicted by the expression to the corresponding numerical solution. The analytical expression is used to predict the impedance response of a lithium-ion cell consisting of a porous LiCoO2 cathode and mesocarbon microbead anode. A qualitative graphical method to identify the co-existence of solid and solution phase transport limitations in the impedance spectra of insertion electrodes is also discussed in the paper
Single-Particle Model for a Lithium-Ion Cell: Thermal Behavior
The single-particle model presented by Santhanagopalan et al. [ J. Power Sources , 156 , 620 (2006)] is extended to include an energy balance. The temperature dependence of the solid phase diffusion coefficient of the lithium in the intercalation particles, the electrochemical reaction rate constants, and the open circuit potentials (OCPs) of the positive and negative electrodes are included in the model. The solution phase polarization is approximated using a nonlinear resistance, which is a function of current and temperature. The model is used to predict the temperature and voltage profiles in a lithium-ion cell during galvanostatic operations. The single-particle thermal model is validated by comparing the simulated voltage and temperature profiles to the results obtained using a distributed porous electrode model. The simulation results from the single-particle thermal model also show good agreement with experimental voltage data obtained from lithium-ion pouch cells under different discharge rates (C/33, C/2 and C) at different temperatures (15, 25, 35, and 45°C )