Suk Seungjae, Yoo Namgyu, Lee Youngsu, Kwon Jaesub, Ahn Heeju, Yoo Seungsu, Lee Jaewoon, Kim Haneul, Bae Joongho, Kim Jongwoo, Jo Chiho, Kim Yong-Tae, Park Kyu-Young
Department of Materials Science and Engineering, Pohang University of Science and Technology (POSTECH), Pohang, Republic of Korea.
Graduate Institute of Ferrous & Eco Materials Technology (GIFT), Pohang University of Science and Technology University, Pohang, Republic of Korea.
Sci Technol Adv Mater. 2025 May 16;26(1):2502324. doi: 10.1080/14686996.2025.2502324. eCollection 2025.
While high-voltage operation of mid-Ni layered oxide cathodes in full-cell Li-ion batteries is essential for achieving high energy density, it inevitably accelerates electrode degradation, ultimately resulting in capacity loss. However, the underlying degradation mechanisms under high-voltage conditions remain poorly understood. In this study, we reveal that anode slippage - induced by cross-talk-driven surface degradation - is the dominant factor in capacity fade during high-voltage (4.35 or 4.40 V) cycling of single-crystal mid-Ni layered oxide (SC-NCM)/graphite pouch full-cells. Electrochemical and post-mortem analyses show that, although high-voltage operation induces cathode surface degradation, including lattice oxygen loss and phase transitions, its direct impact on capacity loss is relatively minor compared to that of the anode. Instead, anode degradation is primarily caused by cross-talk effects from cathode Ni dissolution, which promote the accumulation of irreversible organic byproducts - such as LiO and LiCO - within the solid electrolyte interphase (SEI) layer of the graphite anode. This leads to increased resistance and reduced anode electrochemical activity, disrupting electrode balance and accelerating full-cell capacity fade. These findings highlight the critical role of anode degradation in high-voltage operation and emphasize the importance of mitigating cross-talk effects. A comprehensive understanding of cross-talk-induced anode slippage is therefore critical for the rational design of high-voltage mid-Ni full-cell systems with long-term durability.
虽然锂离子全电池中高镍层状氧化物阴极的高压运行对于实现高能量密度至关重要,但它不可避免地会加速电极退化,最终导致容量损失。然而,高压条件下潜在的退化机制仍知之甚少。在本研究中,我们揭示了由串扰驱动的表面退化引起的阳极滑移是单晶高镍层状氧化物(SC-NCM)/石墨软包全电池在高压(4.35或4.40 V)循环过程中容量衰减的主要因素。电化学和失效分析表明,尽管高压运行会导致阴极表面退化,包括晶格氧损失和相变,但其对容量损失的直接影响与阳极相比相对较小。相反,阳极退化主要是由阴极镍溶解的串扰效应引起的,这会促进不可逆有机副产物(如LiO和LiCO)在石墨阳极的固体电解质界面(SEI)层中积累。这导致电阻增加和阳极电化学活性降低,破坏电极平衡并加速全电池容量衰减。这些发现突出了阳极退化在高压运行中的关键作用,并强调了减轻串扰效应的重要性。因此,全面了解串扰引起的阳极滑移对于合理设计具有长期耐久性的高压高镍全电池系统至关重要。