Stationary Oxygen Vacancy Construction toward a Superior-Performance Ultrahigh Nickel Single-Crystal Cathode.

IF 15.8 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY
ACS Nano Pub Date : 2025-07-10 DOI:10.1021/acsnano.5c05412
Yongzhi Liang,Haoyu Xue,Minzhi Zhan,Hongbin Cao,Zhongxing Xu,Tongchao Liu,Xinghan Chen,Jiajie Liu,Shunning Li,Feng Pan,Xinghua Tan
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引用次数: 0

Abstract

Oxygen vacancies exert a complex and profound influence on the layered cathodes, especially those with ultrahigh nickel content. They can facilitate lithium-ion transport and enhance electronic conductivity, while aggressive oxygen vacancy formation causes structural degradation and electrolyte decomposition. Herein, taking ultrahigh nickel single-crystal LiNi0.92Co0.06Mn0.02O2 (SC-Ni92) as a model material, we propose a pinning strategy to harness the benefits of oxygen vacancies while mitigating their detrimental effects. Through a carefully controlled thermal process, both oxygen vacancies and pinning atoms are successfully introduced into the surface region. The resulting anchored oxygen vacancies, capitalizing on their inherent advantages, improve conductivity and lithium-ion diffusion. Simultaneously, the neighboring pinning atoms effectively increase the migration barrier and suppress the adverse effects of these vacancies, including electrolyte decomposition and structural degradation during long-term electrochemical cycling. Consequently, oxygen vacancy-anchored single-crystal LiNi0.92Co0.06Mn0.02O2 (SC-Ni92-OV) demonstrates significantly improved high-voltage electrochemical performance, with 86.16% capacity retention after 200 cycles at 4.6 V and 1 C in a half-cell and 90.71% after 300 cycles at 4.5 V and 1 C in a full cell. This study not only provides valuable insights into the chemistry of oxygen vacancy but also introduces a viable strategy for leveraging oxygen vacancies to achieve stable high-voltage performance in ultrahigh nickel single-crystal cathodes.
制备高性能超高镍单晶阴极的固定氧空位结构。
氧空位对层状阴极的影响是复杂而深刻的,特别是对含镍量超高的层状阴极。它们可以促进锂离子的传输并增强电子导电性,而侵略性氧空位的形成会导致结构降解和电解质分解。本文以超高镍单晶lini0.92 co0.06 mn0.020 o2 (SC-Ni92)为模型材料,提出了一种利用氧空位的优势同时减轻其不利影响的钉接策略。通过精心控制的热过程,氧空位和钉住原子都成功地引入了表面区域。由此产生的锚定氧空位,利用其固有的优势,提高了导电性和锂离子的扩散。同时,邻近的钉住原子有效地增加了迁移屏障,抑制了这些空位在长期电化学循环过程中的不利影响,包括电解质分解和结构降解。因此,氧空位固定的单晶lini0.92 co0.06 mn0.020 o2 (SC-Ni92-OV)具有显著改善的高压电化学性能,在4.6 V和1 C的半电池中循环200次后容量保持率为86.16%,在4.5 V和1 C的全电池中循环300次后容量保持率为90.71%。该研究不仅为氧空位的化学性质提供了有价值的见解,而且为利用氧空位在超高镍单晶阴极中实现稳定的高压性能提供了一种可行的策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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