High-Entropy Rock-Salt Surface Layer Stabilizes the Ultrahigh-Ni Single-Crystal Cathode

IF 15.8 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY ACS Nano Pub Date : 2024-11-28 DOI:10.1021/acsnano.4c13911
Zhongxing Xu, Xinghan Chen, Wenguang Fan, Minzhi Zhan, Xulin Mu, Hongbin Cao, Xiaohu Wang, Haoyu Xue, Zhihai Gao, Yongzhi Liang, Jiajie Liu, Xinghua Tan, Feng Pan
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Abstract

Single-crystalline Ni-rich layered oxides are one of the most promising cathode materials for lithium-ion batteries due to their superior structural stability. However, sluggish lithium-ion diffusion kinetics and interfacial issues hinder their practical applications. These issues intensify with increasing Ni content in the ultrahigh-Ni regime (≥90%), significantly threatening the practical viability of the single-crystalline strategy for ultrahigh-Ni layered oxide cathodes. Herein, by developing a high-entropy coating strategy, we successfully constructed an epitaxial lattice-coherent high-entropy rock-salt layer (∼3 nm) via Zr and Al doping on the surface of the single-crystalline cathode LiNi0.92Co0.05Mn0.03O2 through an in situ modification process. The surface high-entropy rock-salt layer with tailored Ni valence and lattice coherence not only greatly improves lithium-ion diffusion kinetics but also suppresses interface parasitic reactions and surface structural degradations. The high-entropy surface layer-stabilized ultrahigh-Ni single-crystalline cathode (SC-Ni92-ZA) demonstrates significantly improved rate and cycling performances (127.5 mAh g–1 at 20C, capacity retention of 74.9% after 500 cycles at 1C) in a half-cell. The SC-Ni92-ZA exhibits a capacity retention of 87.1% after 600 cycles at 1C in a full-cell. This epitaxial lattice-coherent high-entropy coating strategy develops a promising avenue for developing high-capacity, long-life cathode materials.

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高熵岩盐表面层稳定了超高镍单晶阴极
单晶富镍层状氧化物具有优异的结构稳定性,是最有前途的锂离子电池正极材料之一。然而,缓慢的锂离子扩散动力学和界面问题阻碍了它们的实际应用。这些问题随着超高镍含量(≥90%)的增加而加剧,极大地威胁了超高镍层状氧化物阴极单晶策略的实际可行性。在此,我们开发了一种高熵涂层策略,通过原位改性工艺,在单晶阴极 LiNi0.92Co0.05Mn0.03O2 表面掺杂 Zr 和 Al,成功构建了外延晶格相干的高熵岩盐层(∼3 nm)。具有定制镍价和晶格相干性的表面高熵岩盐层不仅大大改善了锂离子扩散动力学,还抑制了界面寄生反应和表面结构退化。高熵表面层稳定的超高镍单晶正极(SC-Ni92-ZA)在半电池中的速率和循环性能显著提高(20℃时为 127.5 mAh g-1,1℃时循环 500 次后容量保持率为 74.9%)。在全电池中,SC-Ni92-ZA 在 1C 下循环 600 次后的容量保持率为 87.1%。这种外延晶格相干高熵涂层策略为开发高容量、长寿命阴极材料开辟了一条前景广阔的途径。
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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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