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完整後設資料紀錄
DC 欄位 | 值 | 語言 |
---|---|---|
dc.contributor.advisor | 顏溪成 | |
dc.contributor.author | Hsiang-Yao Hsu | en |
dc.contributor.author | 徐祥耀 | zh_TW |
dc.date.accessioned | 2021-06-16T13:22:07Z | - |
dc.date.available | 2014-07-30 | |
dc.date.copyright | 2013-07-30 | |
dc.date.issued | 2013 | |
dc.date.submitted | 2013-07-25 | |
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dc.identifier.uri | http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/61991 | - |
dc.description.abstract | Lithium-ion batteries have the characteristics of high energy densities, high operate voltage, large output power, and high cycle life. In addition, the low self-discharge rates and the long storage life, making lithium-ion batteries well suited for 3C applications and stationary applications. The mathematical modeling of lithium-ion battery has been developed in this study, based on electrochemistry, combined with thermodynamics, transport phenomena, ohm’s law, and electrochemical kinetics, the model systems was simulated by computer-aided software engineering.
The one-dimensional (flow) model was solved by COMSOL 4.3a software, and the Butler–Volmer equation was solved by MATLAB. The results were compared to the P2D model in COMSOL and the experiments which were performed on CR2032 Li-ion cell with various negative electrode materials (KS-6 graphite, Silicon, C-coated Si, and KS-6/Si). Two different approaches have employed to model the insertion of lithium ions into an negative electrode particle: the Fick's second law and the nonlinear diffusion model considering the vacancy effect. Then, the model system was then scaled up to a cylindrical 18650 lithium cobalt oxide cell. By changing the manufacturing parameters, various effects on the batteries performance would be investigated. Using small particles, increasing the diffusion coefficient of lithium in solid state, and less electrode porosity could increase the discharge capacity. The model involving SEI formation has been developed to simulate the capacity fade of 18650 Li-ion batteries in first few cycles. The largest capacity losses due to solid electrolyte interphase (SEI) growth have been found in the first cycle, and were steady in the next several cycles. | en |
dc.description.provenance | Made available in DSpace on 2021-06-16T13:22:07Z (GMT). No. of bitstreams: 1 ntu-102-R00524087-1.pdf: 12342555 bytes, checksum: a031996b86cc4cd79e7debe3aa1ae450 (MD5) Previous issue date: 2013 | en |
dc.description.tableofcontents | 中文摘要 i
Abstract ii 目 錄 iii 圖目錄 v 表目錄 x 第一章 緒論 1 1.1 鋰二次電池的基本概念 2 1.2 鋰二次電池的電極材料 4 1.3 研究動機 7 第二章 文獻回顧 8 2.1 鋰離子電池數學模擬 8 2.1.1 數學模型 10 2.1.2 數值模擬 17 2.1.3 當前重要議題與研究方向 20 2.2 鋰離子電池數學模型 23 第三章 理論分析 31 3.1 濃溶液理論 31 3.2 多孔性電極理論 35 3.3 邊界條件 37 3.4 固相擴散 38 3.5 電極動力學 40 3.6 模型方程式統整 42 3.7 開環電位與SEI(Solid Electrolyte Interfaces)層 43 第四章 數值方法與模擬 45 4.1 有限元素分析 45 4.2 牛頓法求解非線性方程組 50 4.3 求解流程 51 4.3.1 COMSOL系統 51 4.3.2 MATLAB系統 52 4.3.3 計算方法之比較 53 4.4 電池規格與材料參數 55 第五章 結果與討論 57 5.1 SP模型與P2D模型的比較 57 5.2 鋰離子電池數學模擬之無因次群 60 5.3 鈕扣型鋰離子電池數學模擬 63 5.3.1 純KS-6材料之實驗與數學模擬 64 5.3.2 Si與KS-6重量比2:1混合材料之實驗與數學模擬 72 5.3.3 Si與KS-6重量比1:1混合材料之實驗與數學模擬 75 5.3.4 碳包覆矽燒結材料之實驗與數學模擬 77 5.4 圓柱型鋰離子電池數學模擬 83 5.4.1 不同負極材料之18650鋰離子電池數學模擬 86 5.4.2 KS-6負極材料之18650鋰離子電池數學模擬 89 5.4.3 碳包覆矽燒結材料之18650鋰離子電池數學模擬 98 第六章 結論 106 符號說明 108 參考文獻 111 | |
dc.language.iso | zh-TW | |
dc.title | 碳塗佈於矽粒子負極材料之鋰離子電池巨觀與微觀數學模擬 | zh_TW |
dc.title | The Macroscopic and Microscopic Simulation of the Carbon-Coated Si Anode Lithium-ion Batteries | en |
dc.type | Thesis | |
dc.date.schoolyear | 101-2 | |
dc.description.degree | 碩士 | |
dc.contributor.oralexamcommittee | 高振宏,周偉龍 | |
dc.subject.keyword | 鋰離子電池,數學模擬,多孔性電極理論,濃溶液理論,空位效應,容量衰減,固態電解質介面, | zh_TW |
dc.subject.keyword | Li-ion batteries,Simulations,Porous electrode theory,Concentrated solution theory,Vacancy effect,Capacity fade,Solid electrolyte interphase, | en |
dc.relation.page | 124 | |
dc.rights.note | 有償授權 | |
dc.date.accepted | 2013-07-25 | |
dc.contributor.author-college | 工學院 | zh_TW |
dc.contributor.author-dept | 化學工程學研究所 | zh_TW |
顯示於系所單位: | 化學工程學系 |
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