Chen Yue, Zhang Shaohua, Zhao Dongni, You Zhixian, Niu Yubiao, Zeng Liqiang, Mangayarkarasi Nagarathinam, Kolosov Oleg V, Tao Jianming, Li Jiaxin, Lin Yingbin, Zheng Yongping, Zhang Long, Huang Zhigao
College of Physics and Energy, Fujian Normal University, Fujian Provincial Key Laboratory of Quantum Manipulation and New Energy Materials, Fuzhou, 350117, China; Fujian Provincial Engineering Technical Research Centre of Solar-Energy Conversion and Stored Energy, Fuzhou, 350117, China.
College of Physics and Energy, Fujian Normal University, Fujian Provincial Key Laboratory of Quantum Manipulation and New Energy Materials, Fuzhou, 350117, China; College of Physical Science and Technology, Xiamen University, Xiamen, 361000, China.
J Colloid Interface Sci. 2024 Dec 15;676:603-612. doi: 10.1016/j.jcis.2024.07.159. Epub 2024 Jul 21.
The widespread application of LiTiO (LTO) anode in lithium-ion batteries has been hindered by its relatively low energy density. In this study, we investigated the capacity enhancement mechanism of LTO anode through the incorporation of Na cations in an Li-based electrolyte (dual-cation electrolyte). LTO thin film electrodes were prepared as conductive additive-free and binder-free model electrodes. Electrochemical performance assessments revealed that the dual-cation electrolyte boosts the reversible capacity of the LTO thin film electrode, attributable to the additional pseudocapacitance and intercalation of Na into the LTO lattice. Operando Raman spectroscopy validated the insertion of Li/Na cations into the LTO thin film electrode, and the cation migration kinetics were confirmed by ab initio molecular dynamic (AIMD) simulation and electrochemical impedance spectroscopy, which revealed that the incorporation of Na reduces the activation energy of cation diffusion within the LTO lattice and improves the rate performance of LTO thin film electrodes in the dual-cation electrolyte. Furthermore, the interfacial charge transfer resistance in the dual-cation electrolyte, associated with ion de-solvation processes and traversal of the cations in the solid-electrolyte interphase (SEI) layer, are evaluated using the distribution of relaxation time, Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy. Our approach of performance enhancement using dual-cation electrolytes can be extrapolated to other battery electrodes with sodium/lithium storage capabilities, presenting a novel avenue for the performance enhancement of lithium/sodium-ion batteries.
LiTiO(LTO)负极在锂离子电池中的广泛应用受到其相对较低能量密度的阻碍。在本研究中,我们通过在锂基电解质(双阳离子电解质)中引入Na阳离子来研究LTO负极的容量增强机制。制备了无导电添加剂和无粘结剂的LTO薄膜电极作为模型电极。电化学性能评估表明,双阳离子电解质提高了LTO薄膜电极的可逆容量,这归因于额外的赝电容以及Na嵌入LTO晶格。原位拉曼光谱验证了Li/Na阳离子插入LTO薄膜电极,并且通过从头算分子动力学(AIMD)模拟和电化学阻抗谱证实了阳离子迁移动力学,结果表明Na的引入降低了LTO晶格内阳离子扩散的活化能,并提高了双阳离子电解质中LTO薄膜电极的倍率性能。此外,使用弛豫时间分布、傅里叶变换红外光谱和X射线光电子能谱评估了双阳离子电解质中与离子去溶剂化过程和阳离子在固体电解质界面(SEI)层中的穿越相关的界面电荷转移电阻。我们使用双阳离子电解质提高性能的方法可以推广到其他具有钠/锂存储能力的电池电极,为提高锂/钠离子电池的性能提供了一条新途径。