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Analysis and Modeling of Capacity Fading in Lithium Ion Batteries

Title
Analysis and Modeling of Capacity Fading in Lithium Ion Batteries
Authors
Appiah, Williams Agyei
DGIST Authors
Appiah, Williams Agyei; Lee, Yong Min; Ryou, Myung-Hyun
Advisor(s)
이용민
Co-Advisor(s)
Ryou, Myung-Hyun
Issue Date
2020
Available Date
2020-08-06
Degree Date
2020/08
Type
Thesis
Description
Lithium ion batteries, Capacity fade, Physics-based model, Physico chemical model, Chemo-mechanical model.
Abstract
physico-chemical and chemo-mechanical model, are then developed to describe and quantify the identified degradation mechanisms. The developed capacity fade models are used to study the nature of different cell design parameters and adhesive strength on the specific capacity and stability of Li ion cells. A time-effective accelerated capacity fading analysis method for Li ion batteries is proposed using the developed physico-chemical model and a pseudo-two-dimensional model. The developed capacity fade models improve the prediction and quantification of the degradation mechanisms of high energy density electrode active materials. This will enhance the effective integration of high energy density electrode active material into LIBs and thereby resolve the issues related to mileage requirement and reliability of LIBs for EVs. The findings presented in this work is of both technological and commercial interestsThe distinctive intrinsic electrochemical characteristics of lithium ion batteries (LIBs) have made them a suitable energy storage device for many electrical storage applications such as electric vehicles (EVs) and energy storage systems (ESS). Yet, concerns about the mileage requirement, reliability and safety of LIBs for EV application remain a major drawback. To meet the mileage requirements, there is the need to increase the energy density of LIBs for EVs. This can be achieved by replacing the conventional cathode and anode active material with a higher energy density active material. However, these materials suffer from severe capacity fade. The physical and chemical degradation mechanisms for the severe capacity fade are diverse, complicated and interdependent, and very difficult to understand. Yet, there are limited reliable and practical methods for detecting, predicting and quantifying these degradation phenomena. This thesis presents a non-destructive capacity-fading analysis method to identify the various degradation mechanisms of high energy density active materials for Li ion cells. The key objective of this method is the extraction of information on degradation from physics-based model parameters that changes with cycling via a parameter estimation technique. Comprehensive capacity-fading models
Table Of Contents
List of figures ……………………………………………………………… …………xii List of tables …………………………………………………………….…….… …. xvi Nomenclature …………………………………………………………………………xvii 1 Introduction and literature review 1 1.1 Introduction 1 1.2 Post-mortem analysis methods 8 1.2.1 Surface sensitive chemical analysis methods 9 1.2.2 Bulk electrode chemical analysis methods 11 1.2.3 Electrolyte analysis methods 12 1.3 Battery performance-based analysis methods 14 1.3.1 Electrochemical voltage spectroscopy 14 1.3.2 Identification and tracking of model parameters 17 1.4 Capacity fade modeling 19 1.4.1 Empirical modeling method 20 1.4.2 Physics-based models 24 1.5 Focus and objectives 30 1.6 Outline 32 2 Capacity fade analysis of spinel-based cathode materials 34 2.1 Introduction 34 2.2 Experiment 36 2.3 Results and discussion 37 2.3.1 Parameter Estimation 37 2.3.2 Model prediction 41 2.3.3 Analysis of capacity fade 45 2.4 Conclusion 47 3 A capacity fade model for spinel-based cathode materials 48 3.1 Introduction 48 3.2. Model development 50 3.2.1 Modeling of Mn2+ dissolution in the cathode 50 3.2.2 Modeling of CEI formation in the cathode 52 3.2.3 Modeling of the SEI and Mn side reactions at the anode 54 3.3. Parameter estimation 58 3.4. Results and discussion 59 3.5. Conclusion 69 4 Application of capacity fade model: Accelerated cyclic aging analysis 70 4.1 Introduction 70 4.2 Methodology 72 4.2.1 Experimental data collection 73 4.2.2 Simple empirical life model (SELM) development 74 4.3 Results and discussion 74 4.4 Conclusion 83 5 Capacity fade analysis of anode materials with huge volume expansion 84 5.1 Introduction 84 5.2 Experiment 86 5.2.1 Treatment of Cu current collector with Polydopamine 86 5.2.2 Preparation of Electrode 86 5.2.3 Assembling of cell 86 5.2.4 Measurement of electrochemical performance 87 5.3 Results and discussion 87 5.3.1 Parameter Estimation 87 5.3.2 Model Predictions 91 5.3.3 Capacity fade analysis 94 5.4 Conclusion 102 6 A chemo-mechanical degradation model 103 6.1 Introduction 103 6.2 Model development 104 6.2.1 Modeling of SEI formation 105 6.2.2 Modeling of contact resistance 110 6.2.3 Modeling of particle isolation 114 6.2.4 Modeling of Li ions inventory 115 6.2.5 Modeling the effect of the PD interlayer 117 6.2.6 Coupling between lithiation kinetics and mechanical stress 118 6. 3 Pseudo-two-Dimensional (P2D) model – Incorporation 120 6. 4 Results and discussion 121 6.4.1 Model validation 121 6.4.2 Simulation results 123 6. 5 Conclusion 129 7 Application of chemo mechanical model 130 7.1 Introduction 130 7.2 Experiment 132 7.3 Results and discussion 133 7.3.1 Experimental results 133 7.3.2 Model validation 135 7.3.3 Simulation results 137 7.4 Conclusion 145 8 Conclusion and future work 146 8.1 Contributions 146 8.1.1 Multiphysics-based model capacity fade analysis 147 8.1.2 A capacity fade model for spinel-based cathode materials 148 8.1.3 A time effective cyclic accelerated aging analysis framework 148 8.1.4 A chemo mechanical degradation model 149 8.1.5 Practical relevance 150 8.2 Future work 152 8.2.1 Modeling of Ni-rich cathode materials 152 8.2.2 Exploring the negative side of adhesive thin film interlayers 152 8.2.3 Investigation into degradation mechanisms of large format Li ion cells 153 8.2.4 Short term future research 153 References 158 Appendix A 174 A.1 Model development: SEI formation at cathode 174 A.2 Transport equations 175 Appendix B 179 B.1 Expressions 179 Appendix C 181 C.1 Li ions inventory in Si electrode 181 C.2 Effect of polydopamine design on degradation parameters 181 List of figures 1.1. Ragonne plot of various cell chemistries 2 1.2. Specific energy density from pack to materials level 3 1.3. Degradation mechanism of Si anodes 5 1.4. Layered-to-spinel transformation of Ni-rich cathode materials 6 1.5. Correlation between (a) voltage profile and (b) IC and (c) DV 15 1.6. Degradation mechanisms in Li-ion cells 19 1.7. Schematic diagram of Li ion battery P2D model 25 1.8. Schematic diagram of single particle model (SPM) 28 2.1. Discharge capacity retention of LiMn2O4/graphite cells at 25 and 60 °C. 37 2.2. Comparison of experimental discharge profiles and model-prediction 38 2.3. Changes in degradation parameters of LiMn2O4/graphite cells 40 2.4. Predicted SOC at the EOD at (a) 25 °C and (b) 60 °C 41 2.5. Extrapolation of the model parameters 42 2.6. Physics-based and empirical model prediction at (a) 25 and (b) 60 °C 43 2.7. The predicted SOCs for the positive and negative electrode at the EOD 44 3.1. Physico-chemical degradation model best fit of experimental data 60 3.2. Correlation between Li ion transport and SOC at 25 °C and 60 °C 62 3.3. Concentration profile of the solvent species at the film/electrode interphase 63 3.4. Film resistance at the end of the discharge in the cathode and anode 64 3.5. Relative volume fraction of the active cathode material at 25 ºC and 60 ºC 65 3.6. (a) Changes in the cell capacity retention at different cut off volatges and, (b) Model best-fit to experimental data . 66 3.7. Cycle performance at different discharge rates . 67 3.8. Relative contribution of degradation mechanisms to capacity fade. 68 4.1. Summary of proposed accelerated cyclic aging analysis framework 73 4.2. Experimental results of discharge-capacity retention of LiMn2O4/graphite cells cycled at temperatures of 25 and 60 ºC 75 4.3. Physics-based model best fit to experimental data 76 4.4. Simulated (a) cycling performance, (b) diffusion coefficient constant of the cathode, (c) cathode electrolyte interphase (CEI) resistance and (d) solid electrolyte interphase (SEI) resistance, at various temperatures 78 4.5. Simulations using SELM and PCM–PCEM at different temperatures. 79 4.6. Dependence of (a) capacity-fade constant, and (b) power-law factor on temperature.. 80 4.7. Qualitative analysis of electrochemical voltage spectroscopy . 81 4.8. Predicted number of cycles at different temperatures as a function of………..83 5.1. Comparison of experimental discharge profiles and model predictions. 88 5.2. The changes of model parameters with cycling 90 5.3. The simulated SOCs for the Si/Li half-cells. 91 5.4. The extrapolation of the physics-based P2D model parameters 92 5.5. Comparison of physics-based and empirical model predictions 93 5.6. The predicted SOCs for the bare and PD-treated Cu current collectors 94 5.7. The formation mechanism of EMDOHC and LiEDC 96 5.8. The percentage of Li ion loss in Si/Li cells 98 5.9. The net loss of Li ions in Si/Li cells 99 5.10. Relative contribution of degradation mechanisms to capacity fade. 101 5.11. Schematic diagram showing the effect of the polydopamine interlayer on the number of isolated particles after several cycles.. 101 6.1. Degradation mechanisms of Si electrode with PD-interlayer between the Cu current collector and the composite electrode. 105 6.2. Block diagram of Li ions inventory in the Si electrode 115 6.3. Schematic diagram of the cross section of the cell modeled in this study 120 6.4. Chemo-mechanical degradation model best of experimental data. 123 6.5. Changes in the film resistance and the surface area. 124 6.6. Correlation between the electron transfer rate constant and number of cycles for the PD-treated and bare Cu current collector. 125 6.7. Changes in (a) initial SOC, (b) SOC at EOC and Simulated fractional Li ion loss in Li/Si cells 126 6.8. Relative contribution of various degradation mechanisms 128 7.1. Schematic diagram of cell designs used in this study 133 7.2. Experimental rate performance and the Peukert coefficient of the Li/Si 134 7.3. Experimental and simulation voltage profiles of the three cells 137 7.4. Simulated salt concentration profiles across the Si composite electrode . 138 7.5. Simulated Li ion concentration in the solid phase across the Si composite 139 7.6. (a) Contact resistance and (b) Adhesive strength . 141 7.7. Specific capacity as a function of cell design parameters. 142 7.8. Effect of PD film design parameters on capacity retention 144 C.1. Li ions inventory in the Si composite electrode . 181 C.2. Effect of adhesion strength between Si composite electron an Cu current collector on (a) contact resistance and (b) Li ions loss to isolation. 181 C.3. Effect of various PD film (a) thickness (coverage = 1), (b) thickness (coverage = 0.8) on the rate constant. 182 C.4. Effect of various PD film coverage on the reaction rate constant. 182 C.5. Effect of PD film coverage on (a) contact resistance and (b) Li ions loss to isolation. 183 List of tables 1.1. The governing equations of P2D model 26 2.1. Design parameters, used in this study. 38 2.2. Mathematical expression used for the extrapolation in Figure 2.5 41 2.3. Empirical model expressions 44 3.1. Model parameters. 58 4.1. Equations for predicting the accelerated capacity-fade 78 5.1. Model parameters used in this study 88 5.2. Empirical model expressions and parameters 93 6.1. Table of parameters used for the model prediction. 121
URI
http://dgist.dcollection.net/common/orgView/200000321089
http://hdl.handle.net/20.500.11750/12153
DOI
https://doi.org/10.22677/thesis.200000321089
Degree
Doctor
Department
Department of Energy Science and Engineering
University
DGIST
Related Researcher
  • Author Lee, Yong Min Battery Materials & Systems LAB
  • Research Interests Electrode; Electrolyte; Separator; Simulation
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Collection:
Department of Energy Science and EngineeringThesesPh.D.


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