Investigating the Influence of Transition Metal Substitution in Lithium Argyrodites on Structure, Transport, and Solid-State Battery Performance

IF 7.2 2区 材料科学 Q2 CHEMISTRY, PHYSICAL Chemistry of Materials Pub Date : 2024-11-02 DOI:10.1021/acs.chemmater.4c02281
Johannes Hartel, Ananya Banik, Md Yusuf Ali, Bianca Helm, Kyra Strotmann, Vasiliki Faka, Oliver Maus, Cheng Li, Hartmut Wiggers, Wolfgang G. Zeier
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Abstract

Lithium argyrodites have gained significant attention as candidates for solid electrolytes in solid-state batteries due to their superior ionic conductivities and favorable mechanical properties. However, during charging, oxidative decomposition reactions occur at the interface between the solid electrolyte and cathode active material, which impede cell performance. In this study, transition metal substitution of the solid electrolyte is investigated with the intention of tuning the composition of the cathode electrolyte interphase (CEI) and thereby improving the cycling performance. Hence, the Li5.5–2xZnxPS4.5Cl1.5 (0 ≤ x ≤ 0.15) and Li6–2xZnxPS5Br (0 ≤ x ≤ 0.15) substitution series are investigated to elucidate how substitution affects structure, Li+ transport, and the performance of the materials as catholytes in solid-state batteries. Corefinement of the neutron and powder X-ray diffraction data unveils the occupation of Li+ positions by Zn2+. This leads to blocking of Li+ transport pathways within the Li+ cages causing a decrease of ionic conductivities along with increasing activation energies for Li+ transport. By using a combination of cycling experiments, impedance spectroscopy and X-ray photoelectron spectroscopy, the composition of the CEI and the state-of-charge dependence of the CEI growth when using Li5.5–2xZnxPS4.5Cl1.5|NCM-83 composites was investigated in half-cells, revealing that Zn2+ substitution leads to faster decomposition kinetics and affects the CEI composition. Overall, this work explores the influence of Li+ substitution by Zn2+ on structure and transport in lithium argyrodites and the potential of transition metal substitutions as means to tune the kinetics of CEI growth, the CEI composition, and thereby cell performance.

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探究锂氩离子中过渡金属取代对结构、传输和固态电池性能的影响
作为固态电池的候选固态电解质,锂炔锂因其优越的离子导电性和良好的机械性能而备受关注。然而,在充电过程中,固态电解质和阴极活性材料之间的界面会发生氧化分解反应,从而影响电池性能。本研究对固体电解质中的过渡金属替代物进行了研究,旨在调整阴极电解质间相(CEI)的成分,从而改善电池的循环性能。因此,研究了 Li5.5-2xZnxPS4.5Cl1.5 (0 ≤ x ≤ 0.15) 和 Li6-2xZnxPS5Br (0 ≤ x ≤ 0.15) 取代系列,以阐明取代如何影响结构、Li+ 传输以及材料在固态电池中作为阴极电解质的性能。对中子和粉末 X 射线衍射数据的核心分析揭示了 Zn2+ 对 Li+ 位置的占据。这导致 Li+ 笼内的 Li+ 传输路径受阻,从而降低了离子电导率,同时增加了 Li+ 传输的活化能。通过结合使用循环实验、阻抗光谱和 X 射线光电子能谱,研究了在半电池中使用 Li5.5-2xZnxPS4.5Cl1.5|NCM-83 复合材料时 CEI 的组成和 CEI 生长的电荷状态依赖性,发现 Zn2+ 取代会导致更快的分解动力学并影响 CEI 的组成。总之,这项研究探讨了 Zn2+ 取代 Li+ 对锂氩气电池结构和传输的影响,以及过渡金属取代作为调整 CEI 生长动力学、CEI 组成从而影响电池性能的手段的潜力。
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来源期刊
Chemistry of Materials
Chemistry of Materials 工程技术-材料科学:综合
CiteScore
14.10
自引率
5.80%
发文量
929
审稿时长
1.5 months
期刊介绍: The journal Chemistry of Materials focuses on publishing original research at the intersection of materials science and chemistry. The studies published in the journal involve chemistry as a prominent component and explore topics such as the design, synthesis, characterization, processing, understanding, and application of functional or potentially functional materials. The journal covers various areas of interest, including inorganic and organic solid-state chemistry, nanomaterials, biomaterials, thin films and polymers, and composite/hybrid materials. The journal particularly seeks papers that highlight the creation or development of innovative materials with novel optical, electrical, magnetic, catalytic, or mechanical properties. It is essential that manuscripts on these topics have a primary focus on the chemistry of materials and represent a significant advancement compared to prior research. Before external reviews are sought, submitted manuscripts undergo a review process by a minimum of two editors to ensure their appropriateness for the journal and the presence of sufficient evidence of a significant advance that will be of broad interest to the materials chemistry community.
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