Pouch Type Lithium-ion Battery Research Articles

Impedance Analysis with Transmission Line Model for Reaction Distribution in a Pouch Type Lithium-Ion Battery by Using Micro Reference Electrode

Electrochemical impedance spectroscopy (EIS) using an equivalent circuit is a powerful tool in the diagnosis of lithium-ion batteries (LIBs). However, LIBs have been increasingly used in applications requiring power higher than that used for conventional LIBs for portable electric devices. Considering this demand for LIBs, the ionic resistances in the electrodes, which raise a reaction distribution under high-power operation, are important. This consequently means EIS analysis should include ionic resistances in the electrodes in equivalent circuits. Additionally, the impedance response of LIBs are too complicated to be analyzed in detail because the impedance response consists of overlapping elemental processes such as chemical reactions and ion migration. This paper therefore presents an analysis of impedance responses, which are independently obtained by a micro reference electrode, by using a transmission line model (TLM) that possesses the ability to count the ionic resistances in the electrodes. Similar to the conventional Randles equivalent circuit, the equivalent circuit with TLM could fit the impedance responses simulated by the equivalent circuit with measured responses. This paper discusses the potential of EIS using an equivalent circuit coupled with a TLM for diagnosis of LIBs in power applications.

Dynamic Electrochemical Impedance Spectroscopy of a Three-Electrode Lithium-Ion Battery during Pulse Charge and Discharge

The dynamic electrochemical impedance spectroscopy (DEIS) of a three-electrode pouch type lithium-ion battery is measured using a series of sine wave perturbations super-imposed on pulse charge and discharge. The DEIS reveals noticeable differences between charge and discharge at frequencies corresponding to the charge transfer reaction. The charge transfer resistance during intercalation is generally found to be larger than that during deintercalation for the battery chemistry in this study. This result is mainly attributed to the decreased Li ion concentration in the electrolyte during intercalation. At low frequencies, an abnormal inductive behavior is also observed. Such abnormality is found to result from the violation of stationary condition, i.e. the state of the battery under pulse charge or discharge deviates significantly from its initial condition for the perturbation of low frequencies. To analytically define the stationary condition, we develop electrochemical models of a single active particle in both time and frequency domain, which describes the transport of lithium ions in both active particle and electrolyte phase and the interfacial charge transfer reactions at their interface. The lower frequency limit is a key parameter to ensure a quasistationary state during the DEIS measurement. An explicit formulation of the stationary condition predicts a positive correlation between the lower frequency limit and the DC pulse current.

Numerical modeling and experimental validation of pouch-type lithium-ion battery

The thermal behavior of pouch-type lithium-ion batteries during discharge and charge cycles is investigated by numerical simulation. A transient thermal model using finite element method software is developed through the modification of an electrochemical-thermal model. The developed model is validated with experimental data. For the experiment, a 304252 pouch cell is fabricated and tested in the laboratory. This model captures the dynamic responses of temperature, and distributions of current density and temperature, during discharge and charge cycles. Our results indicate that the discharge temperature is higher than the charge temperature at cut-off voltage. The temperature distribution upon discharge is similar to that of charge. On the other hand, different temperature distributions are observed at various C rates. The temperature profiles obtained from modeling and experiment are in good agreement.

Real-time displacement and strain mappings of lithium-ion batteries using three-dimensional digital image correlation

This work presents the first application of three-dimensional digital image correlation for real-time displacement and strain analysis of a pouch type lithium-ion battery. During the electrochemical charge–discharge processes, displacements in the x-, y- and z-directions vary at different states-of-charge (SOCs) attributed to the expansion and the contraction of the interior structure. The z-displacement is observed to develop and concentrate at the vicinity of the openings of the jelly-roll structure. By resolving the displacement components, the progression and distribution of the surface strains, including principal and von-Mises strains, are computed in the charge–discharge processes. It is shown that the dominant strains are up to 0.12% in the rolling direction of the jelly-roll structure and distribute uniformly on the x–y plane over the surface.

Potential and Current Distributions in Planar Electrodes of Lithium-Ion Batteries

Two-dimensional distribution of potential and current density in planar electrodes of pouch-type lithium-ion batteries are investigated numerically and analytically. A concentration-independent polarization expression, obtained experimentally, is used to mimic the electrochemical performance of the battery. By numerically solving the charge balance equation on each electrode in conjugation with the polarization expression, the battery behavior during constant-current discharge processes is simulated. The numerical analysis shows that reaction current density between the electrodes remains approximately uniform during most of the discharge process, i.e., when depth-of-discharge varies from 5% to 85%. This observation suggested simplifying the electrochemical performance of the battery such that the charge balance equation on each electrode can be solved analytically to obtain closed-form solutions for potential and current density distributions. The analytical model shows fair agreement with experimental and numerical data at modest computational cost. The model is applicable for both charge and discharge processes, and its application is demonstrated for 20 Ah and 75 Ah prismatic lithium-ion batteries. The analytical model is used to describe electrical conduction in the electrodes, and to investigate the effects of tab design on voltage drop. It is demonstrated that constriction/spreading resistance in current collectors of the considered battery is fairly small; about 10% of the total cell resistance but it is larger than the contribution of bulk resistance which is about 3%. The model confirms that constriction/spreading increase with: decrease in the aspect ratio of the current collector, decrease in the tab width, and increase in the tab eccentricity.

Theoretical Analysis of Potential and Current Distributions in Planar Electrodes of Lithium-ion Batteries

An analytical model is proposed to describe the two-dimensional distribution of potential and current in planar electrodes of pouch-type lithium-ion batteries. A concentration-independent polarization expression, obtained experimentally, is used to mimic the electrochemical performance of the battery. By numerically solving the charge balance equation on each electrode in conjugation with the polarization expression, the battery behavior during constant-current discharge processes is simulated. Our numerical simulations show that reaction current between the electrodes remains approximately uniform during most of the discharge process, in particular, when depth-of-discharge varies from 5% to 85%. This observation suggests to simplify the electrochemical behavior of the battery such that the charge balance equation on each electrode can be solved analytically to obtain closed-form solutions for potential and current density distributions. The analytical model shows fair agreement with numerical data at modest computational cost. The model is applicable for both charge and discharge processes, and its application is demonstrated for a prismatic 20Ah nickel-manganese-cobalt lithium-ion battery during discharge processes.

Lithium Nickel Cobalt Manganese Oxide Synthesized Using Alkali Chloride Flux: Morphology and Performance As a Cathode Material for Lithium Ion Batteries

Li(Ni(0.8)Co(0.1)Mn(0.1))O(2) (NCM811) was synthesized using alkali chlorides as a flux and the performance as a cathode material for lithium ion batteries was examined. Primary particles of the powder were segregated and grown separately in the presence of liquid state fluxes, which induced each particle to be composed of one primary particle with well-developed facet planes, not the shape of agglomerates as appears with commercial NCMs. The new NCM showed far less gas emission during high temperature storage at charged states, and higher volumetric capacity thanks to its high bulk density. The material is expected to provide optimal performances for pouch type lithium ion batteries, which require high volumetric capacity and are vulnerable to deformation caused by gas generation from the electrode materials.