Study of Capacity Fade of Lithium-Ion Polymer Battery with Continuous Cycling & Power Performance Modeling of Energy Storage Devices

• Other Authors: Moss, Pedro L. (authoraut)
• Format: Others
• Language: English; English
• Published: Florida State University
• Subjects: Electrical engineering; Computer engineering
• Online Access: http://purl.flvc.org/fsu/fd/FSU_migr_etd-2227

Thus far, capacity fade has been ascribed to various mechanisms that include (i) the dissolution of highly resistive surface films on the electrode surface which result from side reactions; (ii) loss in active electrode materials; (iii) phase change in the electrode structure; (iv) loss of electrode contact with the current collector that can lead to complete cell failure. If accurate dynamic prediction models for batteries are to be achieved through the incorporation of the mechanisms of capacity fade, it is important to quantify the contribution of capacity fade to each mechanism. To quantify capacity fade to various mechanism to the overall impedance of the cell, we investigate a complete electrochemical cell for morphological change at the electrode/electrolyte interface and the change in electrode structural after prolong cycling using scanning electron microscopy (SEM), transmission line microscopy (TEM), x-ray diffraction (XRD). Analyses were performed using commercial lithium-ion polymer cell UP383562A (Sony Co.). The electrochemical charge discharge performance was studied using conventional galvanostatic/potentostatic techniques. Fitting techniques using an electrical equivalent circuit was applied to the electrochemical impedance spectra (EIS) using the method of non linear least square fitting (NLLS). Parameter evaluations from the equivalent circuit show that with extended cycling there is a large increase in the impedance of the solid electrolyte impedance, charge transfer resistance and ionic impedance. SEM analysis on the individual electrodes shows that during charge-discharge cycling, thick surface films are deposited on the negative (graphite) electrode surface. These surface films including LiF, Li2CO3 etc. are known to increase the internal impedance of the cell which result in reduce cell performance. No surface films were observed on the cathode (Li1-xCoO2) electrode surface, however, XRD analysis show the development of some structural defects which are believed to contribute significantly to the overall increase in cell impedance with continuous insertion and extraction of Li ions. The equivalent circuit model obtained from the EIS in the frequency domain can be mapped to a time domain equivalent circuit to accurately represent the dc non-linear behavior, dynamic and transient response of the lithium-ion polymer and electrochemical double layer capacitors (EDLC). More importantly, these models demonstrated that an accurate estimation of the power and energy density relationship in terms of Ragone plots can be obtained. === A Dissertation Submitted to the Department of Electrical and Computer Engineering in Partial Fulfillment of the Requirements for the Degree of Doctor of Philosophy. === Spring Semester, 2008. === April 11, 2008. === Matlab, NMR, Simulink, Power Performance, Transmission Line, Impedance model, Strafi, Charge === Includes bibliographical references. === Jim P. Zheng, Professor Directing Dissertation; Juan C. Ordonez, Outside Committee Member; Yan Xin, Committee Member; Simon Foo, Committee Member; Hui Li, Committee Member.