Alternative Anode Materials for a Highly Stable Lithium Sulfur Battery

阳极 电解质 阴极 硫黄 电池(电) 碳纤维 锂(药物) 锂硫电池 材料科学 化学工程 化学 无机化学 复合材料 电极 冶金 医学 功率(物理) 物理 物理化学 量子力学 复合数 工程类 内分泌学
作者
Jan Brückner,Sören Thieme,Holger Althues,Stefan Kaskel
出处
期刊:Meeting abstracts [Institute of Physics]
卷期号:MA2014-04 (3): 548-548
标识
DOI:10.1149/ma2014-04/3/548
摘要

The lithium-sulfur battery system is expected to achieve more than double the gravimetrical energy density as state-of-the-art lithium-ion systems. At the same time the material costs can be significantly decreased due to the abundance and low price of sulfur. What has kept the lithium-sulfur battery from commercialization is its low cycle stability of the system. In our work we demonstrate that the main problem is the metallic lithium anode, which is currently used in most of the publications. The aprotic solvent molecules of the electrolyte are instable versus lithium. When a low amount of electrolyte is used, the cell runs dry and reversible cycling is limited to less than 200 cycles. Using hard carbon anodes we are able to demonstrate that prolonged, reversible cycling can be achieved for more than 1000 cycles. This system enables balanced lithium-sulfur full-cells with a lithium excess of only 10% and a low amount of electrolyte. The sulfur utilization can be increased to 1470 mAh g -1 sulfur (720 mAh g −1 cathode ) by tuning the porosity of the cathode.[1] Our current generation hard carbon anodes achieve a stable areal capacity of 3 mAh cm -2 enabling a combination with high capacity cathodes. Dry processed sulfur cathodes exhibiting an areal loading of 2.5 to 3 mg sulfur cm -2 and sulfur mass loading in the cathode of 68 wt% (including carbon matrix, conductive additive and binder) were applied and resulting full cell results will be discussed. In addition the stable hard carbon anodes can be used to investigate degradation mechanisms in the lithium sulfur battery system. We present results that point toward the fact that nanometer-sized carbon host materials on the cathode side may suffer from increased mechanical degradation. In contrast micrometer-sized porous particles exhibit outstanding cycling performance. Finally new approaches to transfer these results to high capacity anodes, based on Si/C composites will be discussed. FIGURE1 Fig. 1: Cycle stability for a metallic lithium and all-carbon anode versus the same carbon-sulfur cathode at 836 mA g -1 sulfur and a limited amount of electrolyte. [1] J. Brückner et al., Adv. Funct. Mater., 2013. DOI: 10.1002/adfm.201302169.

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
刚刚
九点的晚风完成签到 ,获得积分10
1秒前
灵巧冰绿完成签到,获得积分10
1秒前
xiaoD发布了新的文献求助10
1秒前
隐形曼青的应助被魔修采纳,获得10
2秒前
小泽发布了新的文献求助10
2秒前
wzg666完成签到,获得积分10
2秒前
JXY189发布了新的文献求助10
3秒前
runtang发布了新的文献求助100
3秒前
4秒前
krislan完成签到,获得积分10
4秒前
素影完成签到,获得积分10
5秒前
HaidongZhang完成签到,获得积分10
5秒前
5秒前
5秒前
6秒前
秋风的应助被跳跃的雯采纳,获得10
6秒前
6秒前
科研通AI2S的应助被跳跃的雯采纳,获得30
6秒前
dyhhh的应助被是ok耶采纳,获得10
7秒前
CipherSage的应助被舒心砖头采纳,获得10
9秒前
聪明少年完成签到,获得积分20
9秒前
10秒前
风吹麦浪的应助被mmm采纳,获得10
10秒前
11秒前
11秒前
xigua发布了新的文献求助10
11秒前
molihuakai的应助被粗暴的世倌采纳,获得10
12秒前
七七发布了新的文献求助10
13秒前
13秒前
云边暮下完成签到,获得积分10
13秒前
FashionBoy的应助被Communist采纳,获得10
13秒前
JamesPei的应助被李睿嘉采纳,获得10
13秒前
14秒前
li完成签到,获得积分10
14秒前
老张完成签到,获得积分10
14秒前
凌时爱吃零食的应助被阿峰采纳,获得30
15秒前
dc发布了新的文献求助10
16秒前
17秒前
moonli发布了新的文献求助10
17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
Encyclopedia of Modern Artificial Intelligence 1000
Особенности технологий и методов информационно-психологических войн СССР с Великобританией и США в период 1939-1953 гг 1000
Das Matthäusevangelium: Kapitel 1:1–17 1000
Analyses de reconnaissances de dettes passées devant les échevins d'Ypres (1249-1291) 600
拉伸高分子熔体中缠结行为的模拟和小角中子散射研究 600
Cellulose and Cellulose Derivatives: Synthesis, Modification and Applications 600
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 工程类 有机化学 化学工程 生物化学 物理 复合材料 内科学 催化作用 光电子学 人工智能 细胞生物学 无机化学 物理化学 数学
热门帖子
关注 科研通微信公众号,转发送积分 8140898
求助须知:如何正确求助?哪些是违规求助? 9541016
关于积分的说明 21643341
捐赠科研通 7725055
什么是DOI,文献DOI怎么找? 3421194
关于科研通互助平台的介绍 2546411
邀请新用户注册赠送积分活动 2463316