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High-rate and excellent-cycle performance Li4Ti5O12 electrodes with 3D porous copper foils as current collectors fabricated using a femtosecond laser processing strategy

材料科学 集电器 阳极 电极 多孔性 电解质 电化学 超级电容器 极化(电化学) 电池(电) 飞秒 纳米技术 锂离子电池 复合材料 光电子学 激光器 冶金 光学 化学 功率(物理) 物理化学 物理 量子力学
作者
Quansheng Li,Xuesong Mei,Xiaofei Sun,Yanbin Han,Bin Liu,Zikang Wang,Anastase Ndahimana,Jianlei Cui,Wenjun Wang
出处
期刊:Journal of energy storage [Elsevier BV]
卷期号:62: 106915-106915 被引量:22
标识
DOI:10.1016/j.est.2023.106915
摘要

Owing to their excellent structural superiorities of large storage space, high specific surface area and reduced volume expansion during battery charge and discharge cycles, 3D porous current collectors have received much concern in the anode of lithium-ion batteries. However, reasonable designing and efficient manufacturing of 3D porous copper foils as current collectors (PCFCCs) remain a great challenge due to the small thickness, soft texture, and variability of copper foils. These material characteristics make it hard to manufacture 3D micro-structure on copper foils and impede the practical application of lithium-ion batteries in more fields. Herein, an efficient and effective strategy is reported to enhance the electrochemical performance of Li4Ti5O12 (LTO) electrodes via rationally designing and manufacturing 3D porous copper foils as current collectors. As a result, the 3D PCFCCs based LTO electrode displays low electrode polarization, excellent-cycle performance and ultra-high rate capacity. Moreover, the structures of various 3D PCFCCs are systematically studied for the first time, the design of 3D PCFCCs is optimized, and the mechanism of improving battery performance is explored. In addition, the proper micro-nano-pore-structures can facilitate electrolyte penetration and the solvated Li+ transport, and the excellent Li+ transmission ability of 3D PCFCCs is verified by simulation.
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