Kim JeongA, Jeong Harok, Oh Eunchae, Jang Jaewon, Lee Sang Won, Kim Dong-Hyun, Han Sang-Don, Kim Jungpil, Yang Junghoon
Carbon & Light Materials Group, Korea Institute of Industrial Technology, Jeonju 54853, Republic of Korea.
Industrialization Division, Korea Carbon Industry Promotion Agency (KCARBON), 110-11 Banryong-ro, Deokjin-gu, Jeonju 54853, Republic of Korea.
ACS Appl Mater Interfaces. 2024 Oct 16;16(41):56271-56284. doi: 10.1021/acsami.4c09721. Epub 2024 Oct 7.
Many studies on electrode material development for rechargeable batteries have focused on improving the intrinsic physicochemical and electrochemical properties of active materials, but the electrochemical performances of batteries are exhibited by the overall electrode unit consisting of active materials, conductive additives, and a binder. Additionally, the electrodes have undergone an essential calendering process to enhance the physical contact between those components. Therefore, the electrochemical behavior and performance of a cell should be analyzed at the electrode level, as the inherent properties of active materials might be changed in electrode preparation, including the calendaring process and real-operating environments. In this study, we aimed to understand the electrochemical properties of the reduced graphene oxide (RGO)-containing electrodes rather than the RGO-active materials by studying the changes in the RGO electrode before and after the calendering process. Specifically, the study investigates the effect of the calendering process on the electrochemically active interphase formation and electrochemical properties of the RGO electrode. We found that the calendering process deteriorates the electrochemical properties of RGO electrodes by impeding enough electrolyte wetting, limiting the formation of thin and stable solid-electrolyte interphase, and leaving unreacted RGO sheets. Additional experiments with carbon-coated silicon/RGO composite electrodes demonstrate that after the calendering process, the sequential participation of Si/C particles in the electrochemical reaction resulted in much more severe capacity degradation over repeated cycling processes. The studies suggest that fine-controlling the number of RGO sheets and maintaining enough distance between those sheets even after the calendering process are required for the utilization of RGO in rechargeable batteries.
许多关于可充电电池电极材料开发的研究都集中在改善活性材料的固有物理化学和电化学性能上,但电池的电化学性能是由由活性材料、导电添加剂和粘合剂组成的整个电极单元所展现的。此外,电极还经过了必不可少的压延工艺,以增强这些组件之间的物理接触。因此,由于活性材料的固有特性在电极制备过程中(包括压延工艺和实际运行环境)可能会发生变化,所以应该在电极层面分析电池的电化学行为和性能。在本研究中,我们旨在通过研究压延工艺前后还原氧化石墨烯(RGO)电极的变化,来了解含RGO电极而非RGO活性材料的电化学性能。具体而言,该研究调查了压延工艺对RGO电极的电化学活性界面形成和电化学性能的影响。我们发现,压延工艺会阻碍电解质充分润湿,限制薄而稳定的固体电解质界面的形成,并留下未反应的RGO片层,从而使RGO电极的电化学性能恶化。对碳包覆硅/RGO复合电极进行的额外实验表明,在压延工艺之后,Si/C颗粒在电化学反应中的顺序参与导致在重复循环过程中容量下降更为严重。这些研究表明,在可充电电池中利用RGO需要精确控制RGO片层的数量,并即使在压延工艺之后也保持这些片层之间有足够的距离。