Hong Meihua, Lee Subin, Ho Van-Chuong, Lee Daon, Yu Seung-Ho, Mun Junyoung
Department of Energy and Chemical Engineering, Incheon National University, 12-1, Songdo-dong, Yeonsu-gu, Incheon 22012, Republic of Korea.
Department of Chemical and Biological Engineering, Korea University, 145 Anam-ro, Seongbuk-gu, Seoul 02841, Republic of Korea.
ACS Appl Mater Interfaces. 2022 Mar 2;14(8):10267-10276. doi: 10.1021/acsami.1c21952. Epub 2022 Feb 21.
The electrochemical dynamic behavior of the solid electrolyte interface (SEI) formed on LiCoO (LCO) by lithium bis(oxalato)borate (LiBOB) is investigated at various cutoff voltages. Particularly, for layered cathode active materials, various cutoff voltages are used to control the delithiation states; however, systematic investigations of the voltage and SEI are lacking. To increase the practical energy density of the LCO, a high cutoff voltage is pursued to utilize a state of high delithiation. However, this high cutoff voltage causes the electrolyte to undergo side reactions and the crystalline structure changes irreversibly, limiting the cycle life. In a low-voltage environment (<4.7 V), LiBOB improves the initial Coulombic efficiency and cycling performance by forming an effective SEI, which suppresses side reactions. At higher voltage levels (4.7-4.9 V), LiBOB no longer effectively protects the surface, causing the electrochemical performance to decrease rapidly. The main cause of this phenomenon is the decomposition of LiBOB-SEI at a high voltage, as shown by systematic surface and electrochemical analyses comprising linear sweep voltammetry, cyclic voltammetry, and electrochemical impedance spectroscopy. In conclusion, LiBOB can suppress side reactions of the electrolyte by SEI formation, but the SEI decomposes at voltage levels higher than 4.7 V.
研究了双草酸硼酸锂(LiBOB)在LiCoO(LCO)上形成的固体电解质界面(SEI)在不同截止电压下的电化学动力学行为。特别是对于层状正极活性材料,使用不同的截止电压来控制脱锂状态;然而,目前缺乏对电压和SEI的系统研究。为了提高LCO的实际能量密度,人们追求高截止电压以利用高脱锂状态。然而,这种高截止电压会导致电解质发生副反应,并且晶体结构不可逆地变化,从而限制了循环寿命。在低电压环境(<4.7 V)下,LiBOB通过形成有效的SEI来抑制副反应,从而提高初始库仑效率和循环性能。在较高电压水平(4.7 - 4.9 V)下,LiBOB不再有效地保护表面,导致电化学性能迅速下降。通过包括线性扫描伏安法、循环伏安法和电化学阻抗谱在内的系统表面和电化学分析表明,这种现象的主要原因是LiBOB - SEI在高电压下分解。总之,LiBOB可以通过形成SEI来抑制电解质的副反应,但SEI在高于4.7 V的电压水平下会分解。