Zhang Jing, Yue Xinyang, Wu Zeyu, Chen Yuanmao, Bai Yu, Sun Kening, Wang Zhenhua, Liang Zheng
Beijing Key Laboratory of Chemical Power Source and Green Catalysis, School of Chemistry and Chemical Engineering, Beijing Institute of Technology, Beijing 100081, China.
Frontiers Science Center for Transformative Molecules, School of Chemistry and Chemical Engineering, Shanghai Jiao Tong University, Shanghai 200240, China.
Nano Lett. 2023 Oct 25;23(20):9609-9617. doi: 10.1021/acs.nanolett.3c03340. Epub 2023 Oct 16.
Lithium (Li) dendrite growth in a routine carbonate electrolyte (RCE) is the main culprit hindering the practical application of Li metal anodes. Herein, we realize the regulation of the LiPF decomposition pathway in RCE containing 1.0 M LiPF by introducing a "self-polymerizing" additive, ethyl isothiocyanate (EITC), resulting in a robust LiF-rich solid electrolyte interphase (SEI). The effect of 1 vol % EITC on the electrode/electrolyte interfacial chemistry slows the formation of the byproduct LiPOF. Such a LiF-rich SEI with EITC polymer winding exhibits a high Young's modulus and a uniform Li-ion flux, which suppresses dendrite growth and interface fluctuation. The EITC-based Li metal cell using a LiTiO cathode delivers a capacity retention of 81.4% over 1000 cycles at 10 C, outperforming its counterpart. The cycling stability of 1 Ah pouch cells was further evaluated under EITC. We believe that this work provides a new method for tuning the interfacial chemistry of Li metal through electrolyte additives.
常规碳酸盐电解质(RCE)中锂(Li)枝晶的生长是阻碍锂金属负极实际应用的主要原因。在此,我们通过引入一种“自聚合”添加剂异硫氰酸乙酯(EITC),实现了对含1.0 M LiPF₆的RCE中LiPF₆分解途径的调控,从而形成了一种富含LiF的坚固固体电解质界面(SEI)。1体积%的EITC对电极/电解质界面化学的影响减缓了副产物LiPO₂F₂的形成。这种具有EITC聚合物缠绕的富含LiF的SEI表现出高杨氏模量和均匀的锂离子通量,从而抑制了枝晶生长和界面波动。使用Li₄Ti₅O₁₂正极的基于EITC的锂金属电池在10 C下1000次循环后容量保持率为81.4%,优于同类电池。在EITC条件下进一步评估了1 Ah软包电池的循环稳定性。我们相信这项工作为通过电解质添加剂调节锂金属的界面化学提供了一种新方法。