Probing Lithium Metal Microstructures with Dynamic Nuclear Polarization from Lithium Metal

IF 3.4 3区 化学 Q2 CHEMISTRY, PHYSICAL
Marie Juramy,Teresa Insinna,Santiago A. Maldonado-Ochoa,Zora Poujol,Gabriela Horwitz,Clare P. Grey
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Abstract

Lithium metal batteries (LMBs) show strong potential for next-generation energy storage, because of their high theoretical energy density. However, their practical deployment is limited by microstructure and dendrite formation, which raises serious safety and efficiency concerns. A key factor influencing dendrite growth is the passivating film, or solid electrolyte interphase (SEI), that forms at the lithium metal surface. Gaining insight into the SEI is essential for controlling dendrite formation, yet this remains challenging due to its complex composition and disorder. Lithium metal endogenous Dynamic Nuclear Polarization (DNP) offers opportunities to probe the SEI with enhanced sensitivity. In this work, we investigate how dendrite morphology influences both DNP enhancement and polarization transfer mechanisms. We develop a protocol to produce lithium dendrites with controlled morphologies on copper electrodes, and find that DNP efficiency is strongly affected by dendrite morphology and the substate they grow on, primarily through variations in the electron spin relaxation times. For Li dendrites grown on a copper substrate, extremely short relaxation times are seen for some morphologies, which we suggest is due largely to the Cu impurities present at the Li/SEI interface since the effect is more pronounced for the thin dendrites, where electrons travel for shorter distances before encountering a surface impurity. The enhancements also depend on the frequency of the applied microwave radio frequency (rf) irradiation, and the extent of rf penetration into the lithium microstructures. Finally, we explore polarization transfer from lithium metal to surrounding salt species in the SEI, providing insight into the underlying mechanisms.

Abstract Image

用锂金属动态核极化探测锂金属微结构
锂金属电池(lmb)由于具有较高的理论能量密度,在下一代储能领域显示出强大的潜力。然而,它们的实际应用受到微观结构和枝晶形成的限制,这引发了严重的安全性和效率问题。影响枝晶生长的关键因素是在锂金属表面形成的钝化膜或固体电解质界面(SEI)。深入了解SEI对于控制枝晶的形成至关重要,但由于其复杂的组成和无序性,这仍然具有挑战性。锂金属内源性动态核极化(DNP)为提高灵敏度探测SEI提供了机会。在这项工作中,我们研究了枝晶形态如何影响DNP增强和极化转移机制。我们开发了一种在铜电极上生产具有控制形态的锂枝晶的方案,并发现DNP效率受到枝晶形态和它们生长的基态的强烈影响,主要是通过电子自旋弛豫时间的变化。对于生长在铜衬底上的锂枝晶,某些形貌的弛豫时间非常短,我们认为这主要是由于在Li/SEI界面上存在Cu杂质,因为薄枝晶的影响更为明显,电子在遇到表面杂质之前移动的距离更短。增强还取决于应用微波射频(rf)照射的频率,以及rf渗透到锂微结构的程度。最后,我们探索了SEI中从锂金属到周围盐种的极化转移,为潜在的机制提供了见解。
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来源期刊
The Journal of Physical Chemistry C
The Journal of Physical Chemistry C 化学-材料科学:综合
CiteScore
6.50
自引率
8.10%
发文量
2047
审稿时长
1.8 months
期刊介绍: The Journal of Physical Chemistry A/B/C is devoted to reporting new and original experimental and theoretical basic research of interest to physical chemists, biophysical chemists, and chemical physicists.
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