High-voltage liquid electrolytes for Li batteries: progress and perspectives

IF 39 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Xiulin Fan and Chunsheng Wang
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引用次数: 127

Abstract

Since the advent of the Li ion batteries (LIBs), the energy density has been tripled, mainly attributed to the increase of the electrode capacities. Now, the capacity of transition metal oxide cathodes is approaching the limit due to the stability limitation of the electrolytes. To further promote the energy density of LIBs, the most promising strategies are to enhance the cut-off voltage of the prevailing cathodes or explore novel high-capacity and high-voltage cathode materials, and also replacing the graphite anode with Si/Si–C or Li metal. However, the commercial ethylene carbonate (EC)-based electrolytes with relatively low anodic stability of ~4.3 V vs. Li+/Li cannot sustain high-voltage cathodes. The bottleneck restricting the electrochemical performance in Li batteries has veered towards new electrolyte compositions catering for aggressive next-generation cathodes and Si/Si–C or Li metal anodes, since the oxidation-resistance of the electrolytes and the in situ formed cathode electrolyte interphase (CEI) layers at the high-voltage cathodes and solid electrolyte interphase (SEI) layers on anodes critically control the electrochemical performance of these high-voltage Li batteries. In this review, we present a comprehensive and in-depth overview on the recent advances, fundamental mechanisms, scientific challenges, and design strategies for the novel high-voltage electrolyte systems, especially focused on stability issues of the electrolytes, the compatibility and interactions between the electrolytes and the electrodes, and reaction mechanisms. Finally, novel insights, promising directions and potential solutions for high voltage electrolytes associated with effective SEI/CEI layers are proposed to motivate revolutionary next-generation high-voltage Li battery chemistries.

Abstract Image

锂电池用高压液体电解质:进展与展望
自锂离子电池问世以来,其能量密度增加了两倍,这主要归功于电极容量的增加。目前,由于电解质的稳定性限制,过渡金属氧化物阴极的容量已接近极限。为了进一步提高锂离子电池的能量密度,最有希望的策略是提高现有阴极的截止电压或探索新的高容量和高压阴极材料,以及用Si/Si -c或Li金属代替石墨阳极。然而,与Li+/Li相比,商用碳酸乙烯(EC)基电解质的阳极稳定性相对较低,为~4.3 V,无法维持高电压阴极。限制锂电池电化学性能的瓶颈已经转向新的电解质成分,以适应具有侵略性的下一代阴极和Si/Si - c或Li金属阳极,因为电解质的抗氧化性和高压阴极上原位形成的阴极电解质间相(CEI)层以及阳极上的固体电解质间相(SEI)层对这些高压锂电池的电化学性能至关重要。本文综述了新型高压电解质体系的研究进展、基本机理、科学挑战和设计策略,重点介绍了电解质的稳定性问题、电解质与电极的相容性和相互作用以及反应机理。最后,提出了与有效SEI/CEI层相关的高压电解质的新见解,有希望的方向和潜在的解决方案,以激发革命性的下一代高压锂电池化学。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Chemical Society Reviews
Chemical Society Reviews 化学-化学综合
CiteScore
80.80
自引率
1.10%
发文量
345
审稿时长
6.0 months
期刊介绍: Chemical Society Reviews is published by: Royal Society of Chemistry. Focus: Review articles on topics of current interest in chemistry; Predecessors: Quarterly Reviews, Chemical Society (1947–1971); Current title: Since 1971; Impact factor: 60.615 (2021); Themed issues: Occasional themed issues on new and emerging areas of research in the chemical sciences
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