Electrochemical performance of ultra-high‑nickel layered oxide cathode synthesized using different lithium sources

IF 3 4区 材料科学 Q3 CHEMISTRY, PHYSICAL
Xuelei Li , Weibo Yang , Yinzhou Wang , Liu Tonggang
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Abstract

Ultra-high‑nickel layered oxide cathodes are extensively explored in lithium-ion battery research owing to their high specific capacity. However, the rapid decline in discharge specific capacity considerably limits their long-term performance. The choice of lithium precursors is crucial in enhancing both the structural and cycle stability of these batteries, yet this aspect has not been adequately addressed in existing studies. In this study, Li2O, LiOH, and Li2CO3 were used as lithium precursors to synthesize LiNi0.92Co0.04Mn0.04O2 (NCM92) cathodes. We compare the structure and electrochemical properties of NCM92 cathode materials prepared with these three lithium precursors, examining a lithium residual layer on the surface of three NCM92 and thus inferring the varying amounts of Li incorporation into the bulk lattice. Our findings highlight the effect of lithium precursors on the rapid degradation of NCM92's discharge capacity. Notably, the NCM92–Li2O cathode demonstrates a higher discharge specific capacity and superior capacity retention after 100 cycles compared to cathodes synthesized with LiOH and Li2CO3. This study provides valuable insights and guidance for further research on ultra-high‑nickel layered oxide cathode materials.
使用不同锂源合成的超高镍层状氧化物正极的电化学性能
超高镍层状氧化物正极因其高比容量而在锂离子电池研究中被广泛探讨。然而,放电比容量的快速下降大大限制了它们的长期性能。锂前驱体的选择对于提高这些电池的结构稳定性和循环稳定性至关重要,但现有研究并未充分考虑到这一点。本研究使用 Li2O、LiOH 和 Li2CO3 作为锂前驱体合成 LiNi0.92Co0.04Mn0.04O2 (NCM92) 正极。我们比较了用这三种锂前驱体制备的 NCM92 正极材料的结构和电化学特性,研究了三种 NCM92 表面的锂残余层,从而推断出锂在体格中的不同掺入量。我们的研究结果凸显了锂前驱体对 NCM92 放电容量快速衰减的影响。值得注意的是,与用 LiOH 和 Li2CO3 合成的阴极相比,NCM92-Li2O 阴极具有更高的放电比容量,并且在 100 次循环后具有更出色的容量保持能力。这项研究为进一步研究超高镍层状氧化物阴极材料提供了宝贵的见解和指导。
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来源期刊
Solid State Ionics
Solid State Ionics 物理-物理:凝聚态物理
CiteScore
6.10
自引率
3.10%
发文量
152
审稿时长
58 days
期刊介绍: This interdisciplinary journal is devoted to the physics, chemistry and materials science of diffusion, mass transport, and reactivity of solids. The major part of each issue is devoted to articles on: (i) physics and chemistry of defects in solids; (ii) reactions in and on solids, e.g. intercalation, corrosion, oxidation, sintering; (iii) ion transport measurements, mechanisms and theory; (iv) solid state electrochemistry; (v) ionically-electronically mixed conducting solids. Related technological applications are also included, provided their characteristics are interpreted in terms of the basic solid state properties. Review papers and relevant symposium proceedings are welcome.
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