提高单晶富镍阴极的结构稳定性,提高袋状电池的可循环性

IF 16 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Youqi Chu, Gemeng Liang, Yongbiao Mu, Qimeng Zhang, Yan Hu, Anjie Lai, Huicun Gu, Qing Zhang*, Lin Zeng* and Chenghao Yang*, 
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引用次数: 0

摘要

单晶LiNi0.9Co0.05Mn0.05O2 (SCNCM90)正极材料在循环过程中经历了持续的容量退化,主要是由于不可逆的结构转变和氧损失。这些变化是由于阴离子和阳离子氧化还原反应导致层内和层间过渡金属离子的局部调整所驱动的。在本研究中,硒(Se)和钛(Ti)同时加入到SCNCM90结构中,增强了结构稳定性,抑制了晶格氧的不可逆反应,减轻了电荷末端相变引起的严重内部应变。此外,SCNCM90阴极中的Se/Ti结构调节降低了Li+的迁移屏障,抑制了循环过程中Li/Ni阳离子的混合,进一步稳定了SCNCM90的结构。深充电过程中o型过渡金属- se键的形成可以减少Oα - (α <)的向外迁移;2)提高氧空位形成能,从而提高SCNCM90内阴离子和阳离子氧化还原过程的稳定性。Ti4+促进SCNCM90表面形成纳米级阳离子混合相层,增强了H2-H3相变的可逆性。此外,内部应变的减轻和晶格氧稳定性的增强对SCNCM90阴极的长期循环稳定性有显著的促进作用。因此,改性材料在1℃、2.8-4.5 V下循环500次后,容量保持率达到87.6%,而未掺杂的阴极仅为61.4%。采用SCNCM90-0.6ST||石墨电极的2.83 Ah袋状电池具有超过500次循环的长循环寿命,在3-4.25 V范围内,在1c条件下容量损失仅为3.1%。这项工作表明,通过提高结构稳定性来减轻颗粒破裂和抑制氧释放对于进一步改进富镍层状阴极材料至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Enhanced Structural Stability of Single-Crystalline Ni-Rich Cathode Enables Improved Cyclability in Pouch Cells

Enhanced Structural Stability of Single-Crystalline Ni-Rich Cathode Enables Improved Cyclability in Pouch Cells

Single-crystalline LiNi0.9Co0.05Mn0.05O2 (SCNCM90) cathode materials experience continuous capacity degradation during cycling, primarily due to irreversible structural transformations and oxygen loss. These alterations are driven by the local adjustment of in-layer and interlayer transition metal ions as a result of anionic and cationic redox reactions. In this study, selenium (Se) and titanium (Ti) were simultaneously incorporated into the SCNCM90 structure to enhance structure stability, inhibit the irreversible reactions of lattice oxygen, and mitigate the severe internal strain induced by phase transformations near the end of the charge. Moreover, Se/Ti structure regulation in the SCNCM90 cathode reduces the Li+ migration barrier, suppresses Li/Ni cation mixing during cycling, and further stabilizes the structure of SCNCM90. The formation of O-transition metal -Se bonds during deep charging can reduce the outward migration of Oα (α < 2) and increase the oxygen vacancy formation energy, thereby improving the stability of anionic and cationic redox processes within SCNCM90. Ti4+ promotes the formation of a nanoscale cationic mixed-phase layer on the surface of SCNCM90, enhancing the reversibility of the H2–H3 phase transition. Additionally, the alleviation of internal strain and the enhanced stability of lattice oxygen significantly contribute to the long-term cyclic stability of SCNCM90 cathodes. Hence, the modification material achieves a capacity retention of 87.6% after 500 cycles at 1 C with 2.8–4.5 V, compared to only 61.4% for the undoped cathode. A 2.83 Ah pouch cell with SCNCM90-0.6ST||graphite electrodes demonstrates a long cycle life of over 500 cycles, with only a 3.1% capacity loss at 1 C within 3–4.25 V. This work reveals that the mitigation of particle cracking and the suppression of oxygen release by enhancing structural stability are crucial for further improvements in Ni-rich layered cathode materials.

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来源期刊
ACS Nano
ACS Nano 工程技术-材料科学:综合
CiteScore
26.00
自引率
4.10%
发文量
1627
审稿时长
1.7 months
期刊介绍: ACS Nano, published monthly, serves as an international forum for comprehensive articles on nanoscience and nanotechnology research at the intersections of chemistry, biology, materials science, physics, and engineering. The journal fosters communication among scientists in these communities, facilitating collaboration, new research opportunities, and advancements through discoveries. ACS Nano covers synthesis, assembly, characterization, theory, and simulation of nanostructures, nanobiotechnology, nanofabrication, methods and tools for nanoscience and nanotechnology, and self- and directed-assembly. Alongside original research articles, it offers thorough reviews, perspectives on cutting-edge research, and discussions envisioning the future of nanoscience and nanotechnology.
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