Ma Bingyuan, Agrawal Shubham, Gopal Rajeev, Bai Peng
Department of Energy, Environmental & Chemical Engineering, Washington University in St. Louis, St. Louis, Missouri63130, United States.
Institute of Materials Science and Engineering, Washington University in St. Louis, St. Louis, Missouri63130, United States.
ACS Appl Mater Interfaces. 2022 Dec 14;14(49):54708-54715. doi: 10.1021/acsami.2c16090. Epub 2022 Dec 1.
The fast-charging capability is critical for the wide adoption of electric vehicles (EVs), which, however, can result in lithium (Li) plating on the graphite anode and thus aggravate cell degradation and increase the safety risk. Li plating is also prone to occur during charging at low temperatures. In this work, we fabricate Li-ion full cells in transparent glass capillaries to probe the real-time dynamic evolution of the lithiated phases throughout the graphite anode toward the onset of lithium plating during fast charging and under low temperatures. We observed that Li plating can occur well before 70% state of charge (SOC), even at a low C-rate and at room temperature. Our experiments provide the direct proof that subtle features in the electrochemical responses are caused by the Li plating, which can be utilized to improve battery management strategy. Mathematical simulations confirm that the local overpotential due to the strong concentration polarization is the root cause of the axial reaction heterogeneity in the graphite anode and the Li plating on the fully lithiated particles.
快速充电能力对于电动汽车的广泛应用至关重要,然而,这可能导致锂在石墨阳极上沉积,从而加剧电池退化并增加安全风险。在低温充电期间也容易发生锂沉积。在这项工作中,我们在透明玻璃毛细管中制造锂离子全电池,以探究在快速充电和低温条件下,整个石墨阳极中锂化相朝着锂沉积开始的实时动态演变。我们观察到,即使在低充电倍率和室温下,在充电状态(SOC)达到70%之前就可能发生锂沉积。我们的实验提供了直接证据,证明电化学响应中的细微特征是由锂沉积引起的,这可用于改进电池管理策略。数学模拟证实,由于强烈的浓度极化导致的局部过电位是石墨阳极中轴向反应不均匀性以及完全锂化颗粒上锂沉积的根本原因。