X-ray Science Division, Advanced Photon Source, Argonne National Laboratory , 9700 South Cass Avenue, Argonne, Illinois 60439, United States.
Department of Chemistry, University of Illinois at Chicago , Chicago, Illinois 60607, United States.
Nano Lett. 2017 Jun 14;17(6):3452-3457. doi: 10.1021/acs.nanolett.7b00379. Epub 2017 Jun 1.
Capacity fading has limited commercial layered Li-ion battery electrodes to <70% of their theoretical capacity. Higher capacities can be achieved initially by charging to higher voltages, however, these gains are eroded by a faster fade in capacity. Increasing lifetimes and reversible capacity are contingent on identifying the origin of this capacity fade to inform electrode design and synthesis. We used operando X-ray diffraction to observe how the lithiation-delithiation reactions within a LiNiCoAlO (NCA) electrode change after capacity fade following months of slow charge-discharge. The changes in the reactions that underpin energy storage after long-term cycling directly correlate to the capacity loss; heterogeneous reaction kinetics observed during extended cycles quantitatively account for the capacity loss. This reaction heterogeneity is ultimately attributed to intergranular fracturing that degrades the connectivity of subsurface grains within the polycrystalline NCA aggregate.
容量衰减将商业分层锂离子电池电极的容量限制在其理论容量的<70%以下。通过将电池充电至高电压,可以在初始阶段实现更高的容量,然而,这种增益会被更快的容量衰减所侵蚀。要提高电池的寿命和可逆容量,就需要确定容量衰减的原因,以便为电极设计和合成提供信息。我们使用 operando X 射线衍射来观察在经过数月的缓慢充放电后,LiNiCoAlO(NCA)电极中的锂化-脱锂反应在容量衰减后如何变化。在长期循环后,支撑储能的反应的变化与容量损失直接相关;在扩展循环中观察到的异质反应动力学定量解释了容量损失。这种反应异质性最终归因于晶间断裂,破坏了多晶 NCA 聚集体中次表面颗粒的连通性。