Progress in development of electrolytes for magnesium batteries

电解质 阳极 材料科学 阴极 电池(电) 能量密度 有机自由基电池 储能 纳米技术 商业化 电极 工程物理 电气工程 化学 冶金 工程类 物理 物理化学 法学 功率(物理) 量子力学 政治学
作者
Ramasubramonian Deivanayagam,Brian J. Ingram,Reza Shahbazian‐Yassar
出处
期刊:Energy Storage Materials [Elsevier BV]
卷期号:21: 136-153 被引量:216
标识
DOI:10.1016/j.ensm.2019.05.028
摘要

Over the last few years, there has been an increased interest in developing safe, next-generation battery systems that offer energy densities higher than those of lithium-based batteries. In this context, batteries based on multivalent-ions (Mg2+, Zn2+, Ca2+, and Al3+) have developed their own niche with their capability to achieve at least twice the energy density of monovalent-ion systems such as Li-ion and Na-ion batteries. Among the multivalent-ion battery candidates, magnesium (Mg) batteries appear to be the most viable choice to eventually replace the Li-ion technology because of the high electrode potential, superior safety, and high abundance of Mg-metal. However, the limited development in electrolytes and cathodes has prevented their commercialization to date. There is a lack of suitable electrolytes that can be used at high voltages required for Mg2+ insertion into cathode hosts. The limited compatibility of organic electrolytes with Mg-metal anode is also a challenge, which requires extensive studies of the metal/electrolyte interactions. Such studies over the last two decades were critical in developing state-of-the-art Mg electrolytes that possess voltage windows of >4.0 V and simultaneously be compatible with Mg-metal anodes. Here, we present a review on the development of Mg battery electrolytes, challenges that impede their performance, and promising strategies that have been adopted to address them. We believe that this comprehensive review covering all three categories of Mg electrolytes (liquids, polymers, and solids) would enable researchers to get a quick grasp of the prevailing challenges, and consequently motivate them to develop novel electrolyte candidates.
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
万能图书馆应助lin采纳,获得10
1秒前
123完成签到,获得积分10
3秒前
Orange应助可靠的公爵熊采纳,获得10
4秒前
李爱国应助楼十八采纳,获得10
5秒前
李健的粉丝团团长应助shw采纳,获得10
6秒前
沉静的蜗牛完成签到,获得积分10
6秒前
8秒前
慕青应助lin采纳,获得10
8秒前
温暖的白猫完成签到,获得积分10
11秒前
热干面完成签到,获得积分10
12秒前
彬彬嘉完成签到,获得积分10
12秒前
12秒前
上官若男应助杨文静采纳,获得10
13秒前
辛勤寻凝完成签到,获得积分10
14秒前
浮生完成签到,获得积分10
15秒前
Xin完成签到,获得积分10
15秒前
Jasper应助lin采纳,获得10
15秒前
高海龙完成签到 ,获得积分10
16秒前
脑洞疼应助cellphone采纳,获得10
16秒前
captainHc完成签到,获得积分10
16秒前
长情无心发布了新的文献求助10
16秒前
Vee发布了新的文献求助10
17秒前
浮生发布了新的文献求助10
18秒前
22秒前
Yonina完成签到,获得积分10
23秒前
23秒前
24秒前
25秒前
罗小黑发布了新的文献求助10
27秒前
Yen完成签到,获得积分10
28秒前
李健应助lin采纳,获得10
28秒前
cellphone发布了新的文献求助10
28秒前
sakura完成签到,获得积分10
29秒前
彭于晏应助受伤冰菱采纳,获得10
29秒前
CodeCraft应助微光采纳,获得10
30秒前
30秒前
123发布了新的文献求助10
31秒前
32秒前
老刀完成签到,获得积分10
32秒前
Hello应助Sun采纳,获得10
33秒前
高分求助中
Principles of Economics, 11th Edition 10000
University Physics with Modern Physics, 16th edition 10000
(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
Development of a Bridge Weigh-In-Motion System: A technology to convert the bridge response to the passage of traffic into data on vehicle configurations, speeds, times of travel and weights 1000
Molecular Mechanisms of Photosynthesis, 4th Edition 1000
Organic Reactions, Volume 116 1000
Current concepts in cutaneous toxicity : proceedings of the Fourth Conference on Cutaneous Toxicity, Washington, D.C., May 9-11, 1979 1000
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 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7265624
求助须知:如何正确求助?哪些是违规求助? 8886567
关于积分的说明 18782171
捐赠科研通 6943134
什么是DOI,文献DOI怎么找? 3202965
关于科研通互助平台的介绍 2376073
邀请新用户注册赠送积分活动 2178825