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通过阴极界面工程提高可充电锂离子电池的电化学性能

Enhancing Electrochemical Performances of Rechargeable Lithium-Ion Batteries via Cathode Interfacial Engineering.

作者信息

Kum Lenin W, Gogia Ashish, Vallo Nick, Singh Deependra Kumar, Kumar Jitendra

机构信息

Solid-State Batteries & Integrated Systems Laboratories, Power & Energy Division, Department of Electrical & Computer Engineering, University of Dayton, 300 College Park, Dayton, Ohio 45469-7531, United States.

Materials Research Centre, Indian Institute of Science, Bangalore 560012, India.

出版信息

ACS Appl Mater Interfaces. 2022 Jan 26;14(3):4100-4110. doi: 10.1021/acsami.1c20787. Epub 2022 Jan 11.

Abstract

Lithium-ion batteries (LIBs) have transformed modern electronics and rapidly advancing electric vehicles (EVs) due to their high energy and power densities, cycle-life, and acceptable safety. However, the comprehensive commercialization of EVs necessitates the invention of LIBs with much enhanced and stable electrochemical performances, including higher energy/power density, cycle-life, and operational safety, but at a lower cost. Herein, we report a simple method for improving the high-voltage (up to 4.5 V) charge capability of LIBs by applying a Li-ion-conducting artificial cathode-electrolyte interface (Li-ACEI) on the state-of-the-art cathode, LiCoO (LCO). A superionic ceramic single Li ion conductor, lithium aluminum germanium phosphate (LiAlGe(PO), LAGP), has been used as a novel Li-ACEI. The application of Li-ACEI on LCO involves a scalable and straightforward wet chemical process (sol-gel method). Cycling performance, including high voltage charge, of bare and LAGP-coated cathodes has been determined against the most energy-dense anode (lithium, Li metal) and state-of-the-art carbonate-based organic liquid electrolyte (OLE). The application of an LAGP-based Li-ACEI on LCO displays many improvements: (i) reduced charge-transfer and interfacial resistance; (ii) higher discharge capacity (167.5 vs 155 mAh/g) at 0.2C; (iii) higher Coulombic efficiency (98.9 vs 97.8%) over 100 cycles; and (iv) higher rate capability (143 vs 80.1 mAh/g) at 4C. Structural and morphological characterizations have substantiated the improved electrochemical behavior of bare and Li-ACEI LCO cathodes against the Li anode.

摘要

锂离子电池(LIBs)因其高能量和功率密度、循环寿命以及可接受的安全性,已经改变了现代电子产品,并推动电动汽车(EVs)迅速发展。然而,电动汽车的全面商业化需要发明具有更高且稳定的电化学性能的锂离子电池,包括更高的能量/功率密度、循环寿命和运行安全性,但成本要更低。在此,我们报道了一种通过在最先进的阴极LiCoO₂(LCO)上应用锂离子传导人工阴极-电解质界面(Li-ACEI)来提高锂离子电池高压(高达4.5V)充电能力的简单方法。一种超离子陶瓷单锂离子导体,锂铝锗磷酸盐(LiAlGe(PO₄)₃,LAGP),已被用作新型Li-ACEI。在LCO上应用Li-ACEI涉及一种可扩展且直接的湿化学工艺(溶胶-凝胶法)。已针对能量密度最高的阳极(锂金属,Li)和最先进的碳酸盐基有机液体电解质(OLE),测定了裸阴极和LAGP涂层阴极的循环性能,包括高压充电性能。基于LAGP的Li-ACEI在LCO上的应用显示出许多改进:(i)降低了电荷转移和界面电阻;(ii)在0.2C时具有更高的放电容量(167.5对155 mAh/g);(iii)在100次循环中具有更高的库仑效率(98.9对97.8%);以及(iv)在4C时具有更高的倍率性能(143对80.1 mAh/g)。结构和形态表征证实了裸阴极和Li-ACEI LCO阴极相对于锂阳极的电化学行为得到了改善。

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