Enhanced electrochemical performance of polycrystalline NCM811 cathode at high voltage through Te-doped LiNbO3 coating for lithium-ion batteries

Next Energy Pub Date : 2025-04-01 Epub Date: 2024-11-29 DOI:10.1016/j.nxener.2024.100216
Mohamed M. Abdelaal, Mohammad Alkhedher
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Abstract

Ni-rich oxides with layered structures are considered promising cathode materials for high-voltage lithium-ion batteries due to their high capacity and wide potential window. However, they suffer from volume expansion and contraction, as well as Ni reactivity with electrolyte components, leading to structural degradation and continuous lithium consumption during cycling. In this study, a highly electrically and ionically layer of Te-doped LiNbO3 is coated onto the surface of LiNi0.8Co0.1Mn0.1O2 (NCM811) to protect the crystal structure from cracks and side reactions with the electrolyte at high voltages (4.3 V vs. Li/Li+). Characterization techniques, including X-ray diffraction (XRD), dynamic light scattering (DLS), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and electrochemical impedance spectroscopy (EIS), are employed to analyze the structure, morphology, and electrochemical performance of the coated materials. Results show that the delivered capacity at 0.1 C increases from 192.9 to 210.8 mAh g−1 and the capacity retention at 0.2 C increases from 79.7 to 89.2% after 100 cycles. Moreover, the diffusion coefficient of the coated NCM is 4.6 × 10−13 cm2 s−1, while that of bare NCM is only 1.5 × 10−13 cm2 s−1 due to the reactivity of the coating layer with lithium. These findings provide valuable insights into the design and optimization of cathode materials for next-generation energy storage systems, contributing to the advancement of sustainable and efficient energy technologies.
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通过掺te的LiNbO3涂层提高锂离子电池多晶NCM811阴极的高压电化学性能
具有层状结构的富镍氧化物因其高容量和宽电位窗而被认为是高压锂离子电池极具前景的正极材料。然而,它们受到体积膨胀和收缩的影响,以及Ni与电解质成分的反应性,导致结构退化和循环过程中持续的锂消耗。在本研究中,在LiNi0.8Co0.1Mn0.1O2 (NCM811)表面涂覆了一层高电性和高离子性的te掺杂LiNbO3层,以保护晶体结构在高压(4.3 V vs. Li/Li+)下不发生裂纹和与电解质的副反应。利用x射线衍射(XRD)、动态光散射(DLS)、扫描电子显微镜(SEM)、透射电子显微镜(TEM)和电化学阻抗谱(EIS)等表征技术对涂层材料的结构、形貌和电化学性能进行了分析。结果表明,经过100次循环,0.1 C下的输出容量从192.9 mAh g−1增加到210.8 mAh g−1,0.2 C下的容量保持率从79.7%增加到89.2%。此外,由于涂层与锂的反应性,涂层NCM的扩散系数为4.6 × 10−13 cm2 s−1,而裸NCM的扩散系数仅为1.5 × 10−13 cm2 s−1。这些发现为下一代储能系统正极材料的设计和优化提供了有价值的见解,有助于推动可持续和高效能源技术的发展。
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