逐步细化和界面电场工程使LiNi0.8Co0.1Mn0.1O2/LiFePO4杂化阴极在恶劣条件下稳定循环

IF 19.3 1区 材料科学 Q1 CHEMISTRY, PHYSICAL
Energy Storage Materials Pub Date : 2026-11-01 Epub Date: 2026-10-14 DOI:10.1016/j.ensm.2026.105598
Shiyou Li, Zhipeng Wang, Hongzeng Dou, Chengyu Li, Xingpeng Cai, Juan Bai, Yulong Zhang, Peng Wang, Dongni Zhao, Xiaoming Xie, Xiaoling Cui, Jinshuo Zou
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引用次数: 0

摘要

富镍层状氧化物阴极在高电压深度衰减过程中严重的结构和表面不稳定性限制了它们的高容量优势,特别是在恶劣条件下。与高度稳定的橄榄石阴极混合是一种补充稳定性的有效技术,但如何利用异质界面促进层状氧化物的均匀深度氧化动力学是一个挑战。本文提出了一种界面电场工程策略,通过简单的研磨-煅烧工艺将LiNi0.8Co0.1Mn0.1O2 (NCM811)/ LiFePO4 (LFP)集成在一起,从而合理调节混合阴极中的锂提取,提高电池的稳定性。理论计算和模拟结果表明,LFP在低电压下优先分解为FePO4,在NCM811/FePO4异质界面上产生了一个内置电场,重构了界面电荷分布,有利于Li+的迁移。由此产生的NCM811在高压下的均匀深度衰减有效地抑制了相变、应变积累和微裂纹的产生,同时通过防止寄生副反应和氧气释放减轻了表面劣化,其中减缓了结构演变和加速了电化学动力学过程,并通过原位表征和分析进行了监测和验证。优化后的具有工程异质界面的NP-30阴极(30 wt% LFP)在65 °C和1℃下140次循环后的容量为167.3 mAh g - 1,容量保持率为80.94%,在5℃下200次循环后的容量保持率为81.12%。这项工作不仅为在恶劣条件下稳定富镍阴极建立了可扩展的界面工程策略,而且为下一代高能量密度电池的设计提供了基本原则。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Stepwise delithiation and interfacial electric field engineering enabling stable cycling of LiNi0.8Co0.1Mn0.1O2/LiFePO4 hybrid cathode under harsh conditions
The severe structural and surficial instability of Ni-rich layered oxide cathodes during deep delithiation at high voltages limits their high-capacity advantage, especially under harsh conditions. Blending with highly stable olivine cathodes can be a useful technique to complement stability, however how to exploiting the heterointerface to facilitate the homogenous deep delithiation kinetics of layered oxide is a challenge. Here, we propose an interfacial electric field engineering strategy to integrate LiNi0.8Co0.1Mn0.1O2 (NCM811)/ LiFePO4 (LFP) through a simple grinding-calcination process, enabling rational regulation of lithium extraction in hybrid cathodes and enhancing battery stability. Revealed by theoretical calculation and simulation, the preferential delithiation of LFP into FePO4 at low voltage induces a built-in electric field across the NCM811/FePO4 heterointerface, which reconstructs the interfacial charge distribution and facilitates Li+ migration. The resulting homogenous deep delithiation of NCM811 at high voltage effectively suppresses phase transition, strain accumulation and microcrack generation in the bulk, while alleviating the surface deterioration by preventing parasitic side reactions and oxygen release, where the mitigated structural evolution and accelerated electrochemical kinetic processes are monitored and verified by in-situ characterizations and analysis. The optimized NP-30 cathode (30 wt% LFP) with engineered heterointerface remarkably delivers a capacity of 167.3 mAh g−1 with 80.94% capacity retention after 140 cycles at 65 °C and 1 C, and maintains 81.12% capacity retention after 200 cycles at 5 C. This work not only establishes a scalable interfacial engineering strategy for stabilizing Ni-rich cathodes under harsh conditions, but also provides fundamental design principles for next generation high-energy-density batteries.
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来源期刊
Energy Storage Materials
Energy Storage Materials Materials Science-General Materials Science
CiteScore
33.00
自引率
5.90%
发文量
652
审稿时长
27 days
期刊介绍: Energy Storage Materials is a global interdisciplinary journal dedicated to sharing scientific and technological advancements in materials and devices for advanced energy storage and related energy conversion, such as in metal-O2 batteries. The journal features comprehensive research articles, including full papers and short communications, as well as authoritative feature articles and reviews by leading experts in the field. Energy Storage Materials covers a wide range of topics, including the synthesis, fabrication, structure, properties, performance, and technological applications of energy storage materials. Additionally, the journal explores strategies, policies, and developments in the field of energy storage materials and devices for sustainable energy. Published papers are selected based on their scientific and technological significance, their ability to provide valuable new knowledge, and their relevance to the international research community.
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