Tao Mingming, Chen Xiaoxuan, Lin Hongxin, Jin Yanting, Shan Peizhao, Zhao Danhui, Gao Mingbin, Liang Ziteng, Yang Yong
State Key Laboratory for Physical Chemistry of Solid Surfaces, Collaborative Innovation Center of Chemistry for Energy Materials and Department of Chemistry, College of Chemistry and Chemical Engineering, Tan Kah Kee Innovation Laboratory (IKKEM), Xiamen University, Xiamen 361005, People's Republic of China.
National Engineering Research Center of Lower-Carbon Catalysis Technology, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, People's Republic of China.
ACS Nano. 2023 Dec 12;17(23):24104-24114. doi: 10.1021/acsnano.3c09120. Epub 2023 Nov 16.
The deposition/stripping behavior of lithium metal is intriguing, and the associated formation of inactive lithium at various temperatures remains elusive, which hinders the practical application of lithium metal batteries. Here, utilizing the variable-temperature operando solid-state nuclear magnetic resonance (SS NMR) technique, we reveal the temperature effects on the lithium microstructure evolution in a carbonate-based electrolyte system. In addition, the mass spectrometry titration (MST) method is used to quantify the evolution of inactive lithium components, including dead lithium, solid electrolyte interface (SEI), and lithium hydride (LiH). Combined SS NMR and MST results show that the morphology of lithium metal is reasonably correlated to the amount of inactive Li formed. At low/ambient temperature, the lithium microstructure has a similar evolution pattern, and its poor morphology leads to a large amount of dead lithium, which dominates capacity loss; however, at high temperature large and dense lithium deposits form with less dead Li detected, and the intensified electrolyte consumption in SEI formation is the major cause for capacity loss. Our phase-field simulation results reveal that the compact lithium deposition formed at higher temperature is due to the more uniformly distributed electric field and Li concentration. Lastly, two strategies in forming a dense Li deposit are proposed and tested that show performance-enhancing results.
锂金属的沉积/剥离行为引人关注,而在不同温度下相关的非活性锂形成情况仍不明确,这阻碍了锂金属电池的实际应用。在此,利用变温原位固态核磁共振(SS NMR)技术,我们揭示了温度对基于碳酸盐的电解质体系中锂微观结构演变的影响。此外,采用质谱滴定(MST)方法来量化非活性锂成分的演变,包括死锂、固体电解质界面(SEI)和氢化锂(LiH)。结合SS NMR和MST的结果表明,锂金属的形态与形成的非活性锂的量有合理的相关性。在低温/环境温度下,锂微观结构具有相似的演变模式,其不良形态导致大量死锂,这是容量损失的主要原因;然而,在高温下形成了大而致密的锂沉积物,检测到的死锂较少,并且在SEI形成过程中电解质消耗加剧是容量损失的主要原因。我们的相场模拟结果表明,在较高温度下形成的致密锂沉积物是由于电场和锂浓度分布更均匀。最后,提出并测试了两种形成致密锂沉积物的策略,结果显示性能得到了提升。