Gunnarsdóttir Anna B, Amanchukwu Chibueze V, Menkin Svetlana, Grey Clare P
Department of Chemistry, University of Cambridge, Cambridge CB2 1EW, U.K.
Department of Chemical Engineering, Stanford University, Stanford, California 94305, United States.
J Am Chem Soc. 2020 Dec 9;142(49):20814-20827. doi: 10.1021/jacs.0c10258. Epub 2020 Nov 23.
Capacity retention in lithium metal batteries needs to be improved if they are to be commercially viable, the low cycling stability and Li corrosion during storage of lithium metal batteries being even more problematic when there is no excess lithium in the cell. Herein, we develop NMR metrology to study "anode-free" lithium metal batteries where lithium is plated directly onto a bare copper current collector from a LiFePO cathode. The methodology allows inactive or "dead lithium" formation during plating and stripping of lithium in a full-cell lithium metal battery to be tracked: dead lithium and SEI formation can be quantified by NMR and their relative rates of formation are here compared in carbonate and ether-electrolytes. Little-to-no dead Li was observed when FEC is used as an additive. The bulk magnetic susceptibility effects arising from the paramagnetic lithium metal were used to distinguish between different surface coverages of lithium deposits. The amount of lithium metal was monitored during rest periods, and lithium metal dissolution (corrosion) was observed in all electrolytes, even during the periods when the battery is not in use, i.e., when no current is flowing, demonstrating that dissolution of lithium remains a critical issue for lithium metal batteries. The high rate of corrosion is attributed to SEI formation on both lithium metal and copper (and Cu, Cu reduction). Strategies to mitigate the corrosion are explored, the work demonstrating that both polymer coatings and the modification of the copper surface chemistry help to stabilize the lithium metal surface.
如果锂金属电池要在商业上可行,就需要提高其容量保持率。当电池中没有过量锂时,锂金属电池在储存期间的低循环稳定性和锂腐蚀问题更加严重。在此,我们开发了核磁共振计量学来研究“无阳极”锂金属电池,其中锂直接从磷酸铁锂阴极镀到裸铜集流体上。该方法可以跟踪全电池锂金属电池在锂电镀和剥离过程中不活跃或“死锂”的形成:死锂和固体电解质界面(SEI)的形成可以通过核磁共振定量,并且在此比较了它们在碳酸盐和醚电解质中的相对形成速率。当使用氟代碳酸乙烯酯(FEC)作为添加剂时,几乎没有观察到死锂。利用顺磁性锂金属产生的体磁化率效应来区分锂沉积物的不同表面覆盖情况。在静置期间监测锂金属的量,并且在所有电解质中都观察到锂金属溶解(腐蚀),即使在电池不使用时,即没有电流流动时也是如此,这表明锂的溶解仍然是锂金属电池的一个关键问题。高腐蚀速率归因于锂金属和铜表面都形成了固体电解质界面(以及铜的还原)。探索了减轻腐蚀的策略,这项工作表明聚合物涂层和铜表面化学改性都有助于稳定锂金属表面。