Li Shuang, Jiang Jiangmin, Feng Qilin, Zheng Yun, Chen Yaxin, Ju Zhicheng, Zhuang Quanchao, Wu Kai, Shao Huaiyu, Zhang Xiaogang
Jiangsu Province Engineering Laboratory of High Efficient Energy Storage Technology and Equipments, School of Materials Science and Physics, China University of Mining and Technology, Xuzhou, 221116, China.
Guangdong-Hong Kong-Macau Joint Laboratory for Photonic-Thermal-Electrical Energy Materials and Devices, Institute of Applied Physics and Materials Engineering, University of Macau, Macau, 999078, China.
Small. 2024 Dec;20(51):e2406274. doi: 10.1002/smll.202406274. Epub 2024 Oct 23.
Graphite (Gr) is a low-cost and high-stability anode for lithium-ion batteries (LIBs). However, Gr anode exhibits an obstinate drawback of low initial Coulombic efficiency (ICE), owing to the active lithium loss for the solid electrolyte interphase (SEI) layer. Herein, a straightforward and effective chemical pre-lithiation strategy is proposed to compensate for the lithium loss. A molecular engineering phenanthrene-based lithium-arene complex (Ph-based LAC) reagent is designed by density functional theory (DFT) calculations. The engineering Ph-based reagent enhances the stability of the π-electron system and the electron-donating capacity, resulting in a reduced redox potential to facilitate lithium transfer. The electrochemical distinct of the Ph-based reagent is illustrated, the prelithiation process in a low Li-insertion platform, and the lithiation degree is controllable with the dipping time (ICE = 102%, 3 min). Notably, a denser and homogeneous SEI layer has pre-formed to enhance the Li transport and interface stability. Moreover, the lithium-ion full batteries assemble with LiFePO and NCM811 cathode, which exhibits high ICE (96.5% and 90.3%) and energy density (310 and 333 Wh kg). These findings present a facile and controllable pre-lithiation strategy to compensate for the lithium of LIBs, providing new valuable insights into the design and optimization of battery manufacture.
石墨(Gr)是一种用于锂离子电池(LIBs)的低成本且高稳定性负极材料。然而,由于固体电解质界面(SEI)层的活性锂损失,Gr负极存在初始库仑效率(ICE)低这一顽固缺点。在此,提出了一种直接有效的化学预锂化策略来补偿锂损失。通过密度泛函理论(DFT)计算设计了一种基于分子工程菲的锂芳烃配合物(Ph基LAC)试剂。该基于分子工程的Ph试剂提高了π电子体系的稳定性和给电子能力,导致氧化还原电位降低,有利于锂转移。阐述了Ph试剂的电化学特性、低锂嵌入平台中的预锂化过程,且锂化程度可通过浸渍时间控制(ICE = 102%,3分钟)。值得注意的是,预先形成了更致密且均匀的SEI层,以增强锂传输和界面稳定性。此外,用LiFePO和NCM811正极组装的锂离子全电池表现出高ICE(96.5%和90.3%)和能量密度(310和333 Wh kg)。这些发现提出了一种简便且可控的预锂化策略来补偿LIBs的锂,为电池制造的设计和优化提供了新的有价值的见解。