Activating ultra-low temperature Li-metal batteries by tetrahydrofuran-based localized saturated electrolyte

材料科学 四氢呋喃 溶剂化 电解质 金属 阳极 阴极 离解(化学) 化学工程 极化(电化学) 乙醚 无机化学 冶金 有机化学 物理化学 电极 化学 工程类 溶剂
作者
Yuansheng Lin,Zhanlin Yang,Xiangxin Zhang,Yongchuan Liu,Guolin Hu,Sujing Chen,Yining Zhang
出处
期刊:Energy Storage Materials [Elsevier BV]
卷期号:58: 184-194 被引量:66
标识
DOI:10.1016/j.ensm.2023.03.026
摘要

For realizing the commercialization of Li-metal batteries (LMBs), the discharge-blocking obstacles under ultra-low temperatures must be conquered besides the long-term reversibility. Nevertheless, commercial carbonate-based electrolytes are not only incompatible with the aggressive Li anode, but also have poor fluidity at low temperatures. The prevailing chain-ether-based electrolyte designing tactics, such as the common-used DME, improve the affinity with Li metal to some extent, but the multiple Lewis-acid binding sites of chain ethers are not conducive to the de-solvation of Li+. Herein, for the first time, the cheap cyclic-type tetrahydrofuran (THF) with ultra-low melting point and weak solvating power is adopted for designing an original THF-based localized saturated electrolyte (Tb-LSCE), demonstrating excellent adaptability for low-temperature LMBs. Computational and experimental evidence verify the original solvated structure is modified via the addition of fluorinated antisolvent, further contributing to the Li+-THF de-solvation. Therefore, equipped with Tb-LSCE, the assembled Li-NCM523 cells achieve powerful anti-polarization capability at low temperatures (73.3% discharge capacity retention at -30 °C). Furthermore, the unique solvated sheath structure of Tb-LSCE also regulates the interfacial chemistry and uniformity of Li depositing behavior, highlighted by the outstanding reversibility of Li-Li cells (a long lifespan of exceeding 1600 h at 30 °C and 1100 h at -30 °C, respectively) and Li-NCM523 cells (80.7%, 160 cycles) even remarkably stable operation within 50 cycles (ultra-high cathode loading of 19.7 mg cm−2). This work outlines a cheap and effective electrolyte design solution to activate the potential LMBs under practical conditions, especially those operated under cryogenic environments.
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
阔达丹亦发布了新的文献求助10
刚刚
1秒前
1秒前
1秒前
2秒前
ggb发布了新的文献求助10
2秒前
2秒前
传奇3应助人间刘可爱采纳,获得20
3秒前
3秒前
LY_Qin完成签到,获得积分0
3秒前
打打应助Asher采纳,获得10
3秒前
yq关闭了yq文献求助
3秒前
秦笑天完成签到,获得积分10
3秒前
山风见月完成签到,获得积分20
3秒前
踏实香氛发布了新的文献求助10
4秒前
宝铭YUAN完成签到,获得积分10
4秒前
dew应助摩登兄弟采纳,获得50
5秒前
10086wm发布了新的文献求助10
5秒前
烟花应助QVQ采纳,获得10
5秒前
5秒前
blossom发布了新的文献求助50
6秒前
头哥完成签到,获得积分10
6秒前
景觅波发布了新的文献求助10
6秒前
情怀应助不安的冷荷采纳,获得10
6秒前
科研菜j完成签到,获得积分10
6秒前
诚心的通发布了新的文献求助30
6秒前
7秒前
领导范儿应助文艺的梦秋采纳,获得10
7秒前
7秒前
7秒前
7秒前
星辰大海应助小次之山采纳,获得50
8秒前
跳跃乘风完成签到,获得积分10
8秒前
8秒前
8秒前
王晋辉发布了新的文献求助10
9秒前
ashelya完成签到,获得积分10
9秒前
盘子完成签到,获得积分10
9秒前
Savior应助大力翠丝采纳,获得10
9秒前
李健应助不枯萎的花采纳,获得10
9秒前
高分求助中
卤化钙钛矿人工突触的研究 1000
Engineering for calcareous sediments : proceedings of the International Conference on Calcareous Sediments, Perth 15-18 March 1988 / edited by R.J. Jewell, D.C. Andrews 1000
Wolffs Headache and Other Head Pain 9th Edition 1000
Continuing Syntax 1000
Signals, Systems, and Signal Processing 510
Cardiac structure and function of elite volleyball players across different playing positions 500
CLSI H26-A2 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 工程类 有机化学 化学工程 生物化学 计算机科学 物理 内科学 复合材料 催化作用 物理化学 光电子学 电极 细胞生物学 基因 无机化学
热门帖子
关注 科研通微信公众号,转发送积分 6242022
求助须知:如何正确求助?哪些是违规求助? 8065936
关于积分的说明 16834777
捐赠科研通 5320067
什么是DOI,文献DOI怎么找? 2832935
邀请新用户注册赠送积分活动 1810458
关于科研通互助平台的介绍 1666837