Lithium tracer diffusion in ion-beam sputtered nano-crystalline and amorphous LiNi0.33Mn0.33Co0.33O2 films

IF 3 4区 材料科学 Q3 CHEMISTRY, PHYSICAL
Erwin Hüger , Harald Schmidt
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引用次数: 0

Abstract

The LiNi0.33Mn0.33Co0.33O2 compound is a cathode material for Li-ion batteries. Li diffusion in this material directly influences charging/discharging times, power densities, maximum capacities, stress formation and possible side reactions. In the present study, Li tracer self-diffusion is investigated on ion-beam sputtered films after deposition (amorphous) and after crystallization at 700 °C. For the experiments, 7Li isotope enriched films with about 1.5 μm thickness were combined with a 50–90 nm thick 6Li tracer layer with the same chemical composition. Afterwards, the films were diffusion annealed between 100 and 300 °C. For analysis secondary ion mass spectrometry in depth profile mode was applied. The diffusivities of the crystalline films are identical to those of sintered bulk samples within error limits as known from literature and show an activation enthalpy of diffusion about 0.9 eV. In contrast, the diffusivities of the amorphous films are about one order of magnitude lower at 100 °C due to a higher activation enthalpy of diffusion of 1.1 eV. We attribute this higher activation enthalpy to a hindered diffusion in the amorphous state of the two-dimensional ion conductor.

离子束溅射纳米晶和无定形 LiNi0.33Mn0.33Co0.33O2 薄膜中的锂示踪剂扩散
LiNi0.33Mn0.33Co0.33O2 复合物是锂离子电池的阴极材料。锂在这种材料中的扩散直接影响充放电时间、功率密度、最大容量、应力形成和可能的副反应。本研究调查了离子束溅射薄膜在沉积(无定形)和 700 °C 结晶后的锂示踪自扩散情况。在实验中,厚度约为 1.5 μm 的 7Li 同位素富集薄膜与厚度为 50-90 nm、化学成分相同的 6Li 示踪剂层结合在一起。然后,薄膜在 100 至 300 °C 之间进行扩散退火。采用深度剖面模式的二次离子质谱进行分析。结晶薄膜的扩散系数与烧结块状样品的扩散系数相同,误差不超过文献记载的误差范围,并显示出大约 0.9 eV 的扩散活化焓。相比之下,无定形薄膜在 100 °C 时的扩散系数要低一个数量级,这是因为其扩散活化焓较高,达到 1.1 eV。我们将这种较高的活化焓归因于二维离子导体在无定形状态下的扩散受阻。
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
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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