阳离子-阴离子协同作用:用于锂金属电池枝晶抑制和界面增强的CsF添加剂

IF 5.5 3区 材料科学 Q1 ELECTROCHEMISTRY
Hao Deng, Wanjie Xu, Xinle Li, Pengfei Liu, Ding Tang, Sen Huang
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引用次数: 0

摘要

锂金属阳极极高的理论容量使其成为下一代高能量密度储能系统的理想候选者。然而,锂枝晶生长不可控和固体电解质界面层的不稳定性阻碍了其实际应用。本研究提出了一种基于Cs+和F -协同作用的电解质修饰策略,采用低浓度CsF添加剂同时实现均匀锂沉积,并优化SEI的组成。结果表明,Cs+通过静电屏蔽机制优先吸附在锂金属表面的尖端区域,迫使Li+在平坦区域均匀成核,从而有效抑制枝晶的形成。同时,F -促进SEI层内LiF的形成,显著提高界面稳定性。电化学测试表明,在0.5 mA/cm2电流密度下,加入0.05 M CsF可使Li||Cu电池在100次循环后的平均库仑效率从58.9%提高到70.9%,而在1 mA/cm2电流密度下,Li||Li对称电池的循环寿命从100 h显著延长至250 h以上。在NCM622||锂电池中,在1C下循环100次后的容量保持率从38.6%提高到80.6%。x射线光电子能谱和扫描电镜表征证实,CsF诱导的富lif SEI层有效降低界面阻抗,抑制死锂积累。这项工作为开发高性能锂金属电池提供了创新的见解,通过阳离子-阴离子协同调节电解质界面。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Cation-Anion Synergy: CsF Additive for Dendrite Suppression and Interface Reinforcement in Lithium Metal Batteries

Cation-Anion Synergy: CsF Additive for Dendrite Suppression and Interface Reinforcement in Lithium Metal Batteries
The extremely high theoretical capacity of lithium metal anode positions it as an ideal candidate for next-generation high-energy-density energy storage systems. However, its practical application is hindered by uncontrollable lithium dendrite growth and the instability of the solid electrolyte interphase (SEI) layer. This study proposes an electrolyte modification strategy based on the synergetic effect of Cs+ and F, employing low-concentration CsF additives to simultaneously achieve uniform lithium deposition and optimized the composition of SEI. The results reveal that Cs+ preferentially adsorbs at the tip regions of the lithium metal surface via an electrostatic shielding mechanism, forcing Li+ to nucleate uniformly on flat regions, thereby effectively suppressing dendrite formation. Meanwhile, F promotes the formation of LiF within the SEI layer, significantly enhancing interfacial stability. Electrochemical tests revealed that the addition of 0.05 M CsF enhanced the average Coulombic efficiency of Li||Cu cells from 58.9% to 70.9% after 100 cycles at 0.5 mA/cm2, while significantly extending the cycling lifespan of Li||Li symmetric cells from 100 h to over 250 h under 1 mA/cm2 current density. In NCM622||Li cells, the capacity retention after 100 cycles at 1C improves from 38.6% to 80.6%. X-ray photoelectron spectroscopy and scanning electron microscopy characterization confirm that the LiF-enriched SEI layer induced by CsF effectively reduces interfacial impedance and inhibits dead lithium accumulation. This work provides innovative insights into developing high-performance lithium metal batteries through cation-anion synergetic regulation of electrolyte interfaces.
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来源期刊
Electrochimica Acta
Electrochimica Acta 工程技术-电化学
CiteScore
11.30
自引率
6.10%
发文量
1634
审稿时长
41 days
期刊介绍: Electrochimica Acta is an international journal. It is intended for the publication of both original work and reviews in the field of electrochemistry. Electrochemistry should be interpreted to mean any of the research fields covered by the Divisions of the International Society of Electrochemistry listed below, as well as emerging scientific domains covered by ISE New Topics Committee.
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