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dc.contributor.advisor Lee, Ho Chun -
dc.contributor.author Lee, Hye Jin -
dc.date.accessioned 2017-05-10T08:52:44Z -
dc.date.available 2016-02-12T00:00:00Z -
dc.date.issued 2016 -
dc.identifier.uri http://dgist.dcollection.net/jsp/common/DcLoOrgPer.jsp?sItemId=000002231309 en_US
dc.identifier.uri http://hdl.handle.net/20.500.11750/1459 -
dc.description.abstract Despite the huge success of the lithium-ion batteries (LIBs) in the portable electronic devices and electric vehicles (EVs) applications, the fundamental understanding on the electrode/electrolyte interface still remains challenging. The interfacial phenomena are governed by the physico-chemical properties of the electrode surface as well as the nature of electrolyte components.
At the first part of this work, the surface free energy (SFE) analysis is performed for various commercial grade LiMn2O4 (LMO) powders and the three SFE components, Lifshitz van der Waals (γ𝑠LW), acid(γ𝑠+), and base(γ𝑠−), are obtained based on the van Oss-Chaudhary-Good (vOCG) theory. It is revealed that Mn dissolution is strongly correlated with the Lewis acid-base component (γ𝑠AB = 2√γ𝑠+ ∙ γ𝑠− ), which is attributed to the short-range columbic interactions between the Lewis acidic site of LMO surface (γ𝑠+) and the basic electrolyte species (e.g., solvents, anions), and between the Lewis basic site (γ𝑠−) and the acidic electrolyte species (e.g., HF).
At the second part, the SFE analysis is performed to shed some light on surface chemical properties of graphite anode and the solid-electrolyte interphase (SEI) layer formed on it. The edge and basal planes of pristine graphite show relatively high γ+ and γ-, respectively. The presence of SEI layer brings dramatic difference in the SFE properties of the graphite electrodes. In particular, the γ- values becomes one order of magnitude higher. In addition, the SFE values also depend on the types of Li salt employed for SEI formation. LiPF6 and LiFSI solutions form inorganic-rich SEI layer, and thus higher total SFE than the organicrich SEI formed in a LiClO4 solution.
At the last part, various polymers are examined to search a suitable probe solid triplet with a low condition number, which is mandatory to determine the three SFE components of liquid samples. Among the tested combinations, PE/PVF/PMMA set is found to have the lowest condition number, which is rather high compared to that of probe liquid set. Further exploration for better probe solid triplet is needed. ⓒ 2016 DGIST
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dc.description.tableofcontents Ⅰ. Correlation of surface free energy and electrolyte property to assess metal dissolution behavior of LiMn2O4 1--
1.1 Introduction 1--
1.1.1 Overview 1--
1.1.2 Capillary rising method for porous materials 2--
1.2 Experimental 3--
1.2.1 Preparation of LMO electrodes 3--
1.2.2 Metal dissolution 4--
1.2.3 Activation energy of Mn dissolution reaction and Arrhenius equation 5--
1.2.4 Adsorption method 7--
1.3 Results and discussion 11--
1.3.1 Analysis of the morphology of LiMn2O4 11--
1.3.2 Contact angle measurement by sorption and surface energy 12--
1.3.3 Effect of donor number on the Mn dissolution 16--
1.3.4 Effect of HF content and Mn dissolution 19--
1.3.5 Correlation between surface energy components and Mn dissolution 20--
1.4 Conclusions 20--
Ⅱ. Surface energy analysis of pristine and SEI-formed graphite anodes 24--
2.1 Introduction 24--
2.2 Experimental 24--
2.2.1 Surface energy analysis of pristine graphite 29--
2.2.2 SEI formation 31--
2.3 Results 32--
2.3.1 Surface energy analysis of graphite (edge and basal planes) 32--
2.3.2 Surface energy analysis of SEI on the pyrolytic graphite 33--
2.4 Conclusion and future plan 39--
Ⅲ. Solid surface energy analysis of polymers for solid probes 42--
3.1 Introduction 42--
3.2 Experimental 48--
3.3 Results 51--
3.4 Discussion and future plan 54--
References 56
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dc.format.extent 59 -
dc.language eng -
dc.publisher DGIST -
dc.subject LiMn2O4 -
dc.subject Surface free energy -
dc.subject metal dissolution -
dc.subject graphite electrode -
dc.subject SEI -
dc.subject condition number -
dc.subject 표면자유에너지 -
dc.subject 금속용출 -
dc.subject 흑연전극 -
dc.title Correlation Study of Surface Energy of Electrodes and Electrolytes with Lithium Ion Battery Performance -
dc.title.alternative 전극 및 전해질 물질의 표면에너지와 리튬이온배터리 성능의 상관관계 연구 -
dc.type Thesis -
dc.identifier.doi 10.22677/thesis.2231309 -
dc.description.alternativeAbstract 시장의 전자기기와 전기자동차에 대한 큰 수요에도 불구하고, 전극/전해액 계면의 근본적인 이해는 아직 밝혀져야 할 부분이 많다. 계면현상은 전극의 표면과 전해액의 물리화학적 특성에 의해 결정된다.
본 연구의 첫 번째 단원에서는, 다양한 상용 등급의 LiMn2O4(이하 LMO)의 표면자유에너지(이하 SFE)를 van Oss-Chaudhary-Good (이하 vOCG) 이론을 바탕으로 분석하여 Lifshitz van der Waals (γ_s^LW), 산 (γ_s^+), and 염기 (γ_s^-) 로 구분하였다. Mn 용출 현상은 short-range columbic force와 관련된 산-염기 표면에너지와 강하게 연관된 것으로 드러났다. LMO 표면의 산 자리와 전해액의 염기 성질 (e.g., solvents, anions), 그리고 전극의 염기 자리와 전해질의 산 성질 (e.g., HF)은 서로 단거리 coulomb 힘으로 상호작용 하는 경향을 보인다.
두 번째 단원에서는 흑연전극과 흑연전극에 형성된 Solid electrolyte interface(이하 SEI) 층의 SFE를 통해 표면 화학 종을 간접분석 하였다. 흑연전극의Edge 와 basal 면은 각각 γ+ 와 γ-가 높게 나왔다. SEI 층은 흑연전극의 SFE를 크게 바꾸는데, 특히 γ- 값은 10배 가량 증가한다. 또한, SFE 값은 SEI 층 형성에 쓰인 Li 염의 종류에도 영향을 받는다. LiPF6와 LIFSI 용액은 주로 무기물 SEI 층을 형성하고, 그에 따라 LiClO4 용액이 형성한 유기물 SEI 층 보다 높은 SFE를 보였다.
세 번째 단원에서는 낮은 condition number를 가진 고체조합을 찾기 위하여 다양한 고분자 기판을 조사하였다. Condition number는 액체 혹은 고체 조합의 적합도를 평가하는 데 필수적인 척도이다. 현재의 액체조합 보다는 높지만, PE/PVF/PMMA는 가장 낮은 condition number를 보였다. 더 좋은 고체조합을 찾기 위한 추가적인 탐색이 필요하다. ⓒ 2016 DGIST
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dc.description.degree Master -
dc.contributor.department Energy Systems Engineering -
dc.contributor.coadvisor Kang, Joon Goo -
dc.date.awarded 2016. 2 -
dc.publisher.location Daegu -
dc.description.database dCollection -
dc.date.accepted 2016-02-12 -
dc.contributor.alternativeDepartment 대학원 에너지시스템공학전공 -
dc.contributor.affiliatedAuthor Lee, Hye Jin -
dc.contributor.affiliatedAuthor Lee, Ho Chun -
dc.contributor.affiliatedAuthor Kang, Joon Goo -
dc.contributor.alternativeName 이혜진 -
dc.contributor.alternativeName 이호춘 -
dc.contributor.alternativeName 강준구 -
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