Interphase Design for Lithium-Metal Anodes

IF 15.6 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Qidi Wang*, Chenglong Zhao, Shuwei Wang, Jianlin Wang, Fangting Wu, Pierfrancesco Ombrini, Swapna Ganapathy, Stephen Eustace, Xuedong Bai, Baohua Li, Michel Armand*, Doron Aurbach* and Marnix Wagemaker*, 
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Abstract

Electrode–electrolyte interphases are critical determinants of the reversibility and longevity of lithium (Li)-metal batteries (LMBs). However, upon cycling, the inherently delicate interphases, formed from electrolyte decomposition, become vulnerable to chemomechanical degradation and corrosion, resulting in rapid capacity loss and thus short battery life. Here, we present a comprehensive analysis of the complex interplay between the thermodynamic and kinetic properties of interphases on Li-metal anodes, providing insights into interphase design to address these challenges. Direct measurements of ion-transport kinetics across various electrolyte chemistries reveal that interphases with high Li-ion mobility are essential for achieving dense Li deposits. Conversely, sluggish ion transport generates high-surface-area Li deposits that induce Li random stripping and the accumulation of isolated Li deposits. Surprisingly, interphases that support long cycle life do not necessarily require the formation of dense Li deposits but must avoid possible electrochemical/chemical reactions between the Li-metal deposits and electrolytes’ components. By that, in some specific electrolyte systems, isolated Li deposits can recover and electrically rejoin the active Li anodes’ mass. These findings challenge conventional understanding and establish new principles for designing durable LMBs, demonstrating that even with commercial carbonate-based electrolytes, LiNi0.8Co0.1Mn0.1O2||Cu cells can achieve high reversibility.

Abstract Image

锂金属阳极的界面设计
电极-电解质界面是决定锂金属电池可逆性和寿命的关键因素。然而,在循环过程中,由电解质分解形成的固有微妙的界面容易受到化学机械降解和腐蚀,导致容量迅速损失,从而缩短电池寿命。在这里,我们对锂金属阳极上界面相的热力学和动力学性质之间复杂的相互作用进行了全面的分析,为界面相设计提供了见解,以解决这些挑战。对不同电解质化学性质的离子传输动力学的直接测量表明,具有高锂离子迁移率的界面相对于实现致密的锂沉积是必不可少的。相反,缓慢的离子传输产生高表面积的锂沉积,导致锂的随机剥离和孤立锂沉积的堆积。令人惊讶的是,支持长循环寿命的界面并不一定需要形成致密的锂沉积物,但必须避免锂金属沉积物和电解质组分之间可能发生的电化学/化学反应。通过这种方法,在某些特定的电解质体系中,孤立的锂沉积物可以恢复并电性地重新加入活性锂阳极的质量。这些发现挑战了传统的理解,并为设计耐用的lmb建立了新的原则,表明即使使用商业碳酸基电解质,LiNi0.8Co0.1Mn0.1O2||Cu电池也可以实现高可逆性。
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来源期刊
CiteScore
24.40
自引率
6.00%
发文量
2398
审稿时长
1.6 months
期刊介绍: The flagship journal of the American Chemical Society, known as the Journal of the American Chemical Society (JACS), has been a prestigious publication since its establishment in 1879. It holds a preeminent position in the field of chemistry and related interdisciplinary sciences. JACS is committed to disseminating cutting-edge research papers, covering a wide range of topics, and encompasses approximately 19,000 pages of Articles, Communications, and Perspectives annually. With a weekly publication frequency, JACS plays a vital role in advancing the field of chemistry by providing essential research.
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