Review—Development of Advanced Rechargeable Batteries: A Continuous Challenge in the Choice of Suitable Electrolyte Solutions

电解质 电池(电) 锂离子电池的纳米结构 电化学 有机自由基电池 阳极 阴极 电化学窗口 储能 材料科学 纳米技术 电极 化学 电气工程 功率(物理) 离子电导率 工程类 物理 物理化学 量子力学
作者
Evan M. Erickson,Elena Markevich,Gregory Salitra,Daniel Sharon,Daniel Hirshberg,Ezequiel de la Llave,Ivgeni Shterenberg,Ariel Rosenman,Aryeh A. Frimer,Doron Aurbach
出处
期刊:Journal of The Electrochemical Society [Institute of Physics]
卷期号:162 (14): A2424-A2438 被引量:157
标识
DOI:10.1149/2.0051514jes
摘要

Non-aqueous, rechargeable battery development is one of the most important challenges of modern electrochemistry. Li ion batteries are a commercial reality for portable electronics with intensive efforts underway to apply this technology to electro-mobility. Extensive investigations of high energy density Li-sulfur and Li-oxygen systems have also been carried-out. Efforts to promote high energy density power sources for electric vehicles have been accompanied by intensive work on the development of rechargeable sodium and magnesium batteries for load-leveling applications. The electrolyte solution is a key consideration in all batteries determining cell stability, cycle life, and safety. This review discusses the importance of solution selection for advanced, high-voltage, Li ion batteries, sodium ion batteries, as well as Li-sulfur, Li-oxygen and magnesium batteries. Li ion battery standard solutions are discussed and their further optimization is outlined. Limitations of Li metal electrodes are explained. Unique problems in the use of conventional non-aqueous solutions for Li-oxygen batteries, related to intrinsic stability, are delineated. Finally, electrolyte solutions for Mg batteries are briefly reviewed, concluding that only the relatively inert ethereal solutions are suitable for future consideration. Several systems exhibit wide electrochemical windows and reversible behavior with Mg anodes, however compatibility with high-voltage/high-capacity cathodes remains a major challenge.
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
刚刚
科研通AI5应助lancekkk采纳,获得10
刚刚
刚刚
李十完成签到,获得积分10
刚刚
华仔应助贪玩的初雪采纳,获得10
刚刚
贪玩的可乐完成签到,获得积分10
1秒前
CipherSage应助漂亮的素采纳,获得10
1秒前
江海寄馀生完成签到,获得积分10
1秒前
量子星尘发布了新的文献求助10
1秒前
2秒前
2秒前
YJS关闭了YJS文献求助
2秒前
ding应助syrrr要发文章采纳,获得10
3秒前
baochao完成签到 ,获得积分10
3秒前
是然发布了新的文献求助10
3秒前
科研通AI5应助方星采纳,获得10
3秒前
3秒前
3秒前
柳白发布了新的文献求助10
3秒前
永不阴性发布了新的文献求助10
4秒前
李凤凤发布了新的文献求助30
4秒前
mikefei完成签到,获得积分10
4秒前
科研通AI5应助流萤采纳,获得10
5秒前
6秒前
在水一方应助tch采纳,获得10
7秒前
7秒前
fuyuhaoy完成签到,获得积分10
8秒前
你好包包发布了新的文献求助10
8秒前
8秒前
汉堡包应助晶莹黎采纳,获得10
8秒前
哦哦哦发布了新的文献求助10
8秒前
Yyy完成签到,获得积分10
9秒前
柳白完成签到,获得积分10
9秒前
脑洞疼应助结实的保温杯采纳,获得10
9秒前
闪闪的夏之完成签到,获得积分10
10秒前
10秒前
10秒前
10秒前
和谐笙完成签到,获得积分10
10秒前
yyyyzhu应助2032jia采纳,获得10
10秒前
高分求助中
Production Logging: Theoretical and Interpretive Elements 2700
Neuromuscular and Electrodiagnostic Medicine Board Review 1000
Statistical Methods for the Social Sciences, Global Edition, 6th edition 600
こんなに痛いのにどうして「なんでもない」と医者にいわれてしまうのでしょうか 510
Walter Gilbert: Selected Works 500
An Annotated Checklist of Dinosaur Species by Continent 500
岡本唐貴自伝的回想画集 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 物理 生物化学 纳米技术 计算机科学 化学工程 内科学 复合材料 物理化学 电极 遗传学 量子力学 基因 冶金 催化作用
热门帖子
关注 科研通微信公众号,转发送积分 3663432
求助须知:如何正确求助?哪些是违规求助? 3223996
关于积分的说明 9754408
捐赠科研通 2933862
什么是DOI,文献DOI怎么找? 1606458
邀请新用户注册赠送积分活动 758497
科研通“疑难数据库(出版商)”最低求助积分说明 734836