Effect of propylene carbonate-Li+ solvation structures on graphite exfoliation and its application in Li-ion batteries

碳酸丙烯酯 溶剂化 石墨 剥脱关节 电解质 锂(药物) 石墨烯 电化学 插层(化学) 无机化学 锂电池 材料科学 阳极 化学 物理化学 离子 有机化学 纳米技术 电极 离子键合 内分泌学 医学
作者
Pengcheng Shi,Ming-Hsein Lin,Hao Zheng,Xin He,Zoulin Xue,Hongfa Xiang,Chunhua Chen
出处
期刊:Electrochimica Acta [Elsevier BV]
卷期号:247: 12-18 被引量:53
标识
DOI:10.1016/j.electacta.2017.06.174
摘要

The effect of propylene carbonate (PC)-Li+ solvation structures on graphite exfoliation was investigated over a range of concentrations of PC-based electrolytes. At low concentrations of lithium bis(trifluoromethanesulfonyl) imide (LiTFSI) in PC (1.3 M and 2.1 M), the graphite anode was exfoliated. However, the graphite exfoliation could be effectively suppressed when the concentrations of dissolved LiTFSI were increased to 2.5 M and 3.3 M. The results of spectroscopic analyses and density functional theory (DFT) calculations revealed that electrochemical exfoliation of the graphite anode is closely associated with a special spatial configuration of Li+-(PC)n (1 ≤ n ≤ 4) solvation structures at various Li-salt concentrations and corresponding solid electrolyte interface (SEI) film formation mechanisms. When the concentration of LiTFSI increased from 1.3 to 3.3 M, the spatial configuration of Li+-(PC)n (1 ≤ n ≤ 4) solvation gradually changed from a tetrahedron (occupied space of 10.19 Å) to planar (occupied space of 3.05 Å), which reduced the structure change for co-intercalation into the graphite interlayers of Li+-(PC)n (1 ≤ n ≤ 4) solvates. Meanwhile, the affinity between Li+-(PC)n (1 ≤ n ≤ 4) solvation cations and TFSI− anions was increased, leading to the significant contribution of TFSI− anions to SEI formation on the surface of graphite. Additionally, Al corrosion was not of concern in concentrated LiTFSI electrolyte. The 3.3 M LiTFSI/PC concentrated electrolyte exhibits promising electrochemical performance in graphite||LiNi1/3Co1/3Mn1/3O2 full cells.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
我是老大的应助被科研通管家采纳,获得10
刚刚
大个的应助被科研通管家采纳,获得10
1秒前
Hello的应助被科研通管家采纳,获得10
1秒前
科研狗的应助被科研通管家采纳,获得30
1秒前
molihuakai的应助被科研通管家采纳,获得10
1秒前
小二郎的应助被科研通管家采纳,获得10
1秒前
烟花的应助被科研通管家采纳,获得10
1秒前
54189415发布了新的文献求助10
1秒前
CipherSage的应助被科研通管家采纳,获得10
1秒前
1秒前
搜集达人的应助被科研通管家采纳,获得10
2秒前
秋风的应助被科研通管家采纳,获得10
2秒前
无花果的应助被科研通管家采纳,获得10
2秒前
2秒前
丘比特的应助被科研通管家采纳,获得10
2秒前
踏实安波的应助被科研通管家采纳,获得10
2秒前
2秒前
充电宝的应助被科研通管家采纳,获得20
2秒前
2秒前
ZGQ的应助被科研通管家采纳,获得10
3秒前
xzj7789210发布了新的文献求助10
3秒前
深情安青的应助被科研通管家采纳,获得10
3秒前
充电宝的应助被科研通管家采纳,获得10
3秒前
秋风的应助被科研通管家采纳,获得30
3秒前
秋风的应助被科研通管家采纳,获得30
3秒前
慕青的应助被科研通管家采纳,获得10
3秒前
Jasper的应助被科研通管家采纳,获得30
3秒前
wanci的应助被科研通管家采纳,获得10
3秒前
脑洞疼的应助被科研通管家采纳,获得10
4秒前
huiqin完成签到 ,获得积分10
4秒前
李爱国的应助被科研通管家采纳,获得10
4秒前
FashionBoy的应助被科研通管家采纳,获得10
4秒前
4秒前
传奇3的应助被科研通管家采纳,获得10
4秒前
领导范儿的应助被小坏坏采纳,获得10
4秒前
天天快乐的应助被科研通管家采纳,获得10
4秒前
领导范儿的应助被科研通管家采纳,获得10
4秒前
大个的应助被科研通管家采纳,获得10
5秒前
修仙中的应助被科研通管家采纳,获得10
5秒前
mmyhn的应助被科研通管家采纳,获得20
5秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
自動車の空力技術 800
Essentials of Carbohydrate Chemistry and Biochemistry, 4th Edition 800
Organizational Behavior 510
Management and the Arts 510
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
Issues in Task-Based Language Teaching 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 计算机科学 化学工程 工程类 有机化学 物理 复合材料 生物化学 内科学 细胞生物学 基因 遗传学 免疫学 冶金 光电子学 癌症研究
热门帖子
关注 科研通微信公众号,转发送积分 7783934
求助须知:如何正确求助?哪些是违规求助? 9323270
关于积分的说明 20393735
捐赠科研通 7372599
什么是DOI,文献DOI怎么找? 3320836
关于科研通互助平台的介绍 2468807
邀请新用户注册赠送积分活动 2337060