Grain-Boundary-Rich Interphases for Rechargeable Batteries

IF 14.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY Journal of the American Chemical Society Pub Date : 2024-11-08 DOI:10.1021/jacs.4c10650
Qidi Wang, Chenglong Zhao, Xia Hu, Jianlin Wang, Swapna Ganapathy, Stephen Eustace, Xuedong Bai, Baohua Li, Hong Li, Doron Aurbach, Marnix Wagemaker
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Abstract

The formation of stable interphases on the electrodes is crucial for rechargeable lithium (Li) batteries. However, next-generation high-energy batteries face challenges in controlling interphase formation due to the high reactivity and structural changes of electrodes, leading to reduced stability and slow ion transport, which accelerate battery degradation. Here, we report an approach to address these issues by introducing multicomponent grain-boundary-rich interphase that boosts the rapid transport of ions and enhances passivation toward prolonged lifespan. This is guided by fundamental principles of solid-state ionics and geological crystallization differentiation theory, achieved through improved solvation chemistry. Demonstrations showcase how the introduction of the interphase substantially impacts the Li-ion transport across the interphase and the electrode–electrolyte compatibility in cost-effective electrolyte solutions optimized with multiple Li salts. The resulting interphases feature microstructures rich in inorganic grain boundaries with a diverse array of nanosized grains, presenting enhanced Li-ion transport. Comprehensive analyses revealed that this realizes remarkable electrochemical stability over extended cycling periods by inhibiting electrode corrosion, thus holding promise for high-capacity thin-Li-metal, Si-based anodes, and even Li-free anodes when paired with high-capacity oxide cathodes. This work opens new avenues to customize protective interphases on high-capacity electrodes, promoting the development of batteries with the highest energy density using cost-effective electrolytes.

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用于充电电池的富晶粒边界相位
在电极上形成稳定的间相对于可充电锂(Li)电池至关重要。然而,由于电极的高反应性和结构变化,下一代高能电池在控制相间形成方面面临挑战,导致稳定性降低和离子传输缓慢,从而加速电池降解。在此,我们报告了一种解决这些问题的方法,即引入富含多组分晶界的间相,从而促进离子的快速传输,并增强钝化以延长使用寿命。这是以固态离子学和地质结晶分化理论的基本原理为指导,通过改进溶解化学来实现的。演示展示了相间层的引入如何对锂离子在相间层的传输以及在使用多种锂盐优化的高性价比电解质溶液中的电极-电解质兼容性产生重大影响。由此产生的相间层具有富含无机晶界的微观结构,并具有各种纳米尺寸的晶粒,从而增强了锂离子的传输。综合分析表明,这种材料通过抑制电极腐蚀,在较长的循环时间内实现了显著的电化学稳定性,因此有望用于高容量薄锂基金属阳极、硅基阳极,甚至在与高容量氧化物阴极配对时用于无锂电池阳极。这项研究开辟了在高容量电极上定制保护性相间层的新途径,促进了使用经济高效的电解质开发能量密度最高的电池。
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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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