Tailoring a Glass Network Structure through Addition of Transition Metal Oxides to Enhance Ionic Conductivity in Phosphate Glasses

IF 4.3 2区 化学 Q1 CHEMISTRY, INORGANIC & NUCLEAR
Sanja Renka, Grégory Tricot, Tomáš Hostinský, Petr Mošner, Ladislav Koudelka, Ahmed Ibrahim, Shiro Kubuki, Zdravko Siketić, Ana Šantić
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Abstract

In the development of oxide glass-based electrolytes and electrodes for solid-state batteries, high ionic conductivity represents an ultimate challenge. One way of increasing the ionic conductivity in these materials is to increase the mobility of ions through the addition of transition metal oxides. In this study, we report a significant enhancement of lithium-ion conductivity due to structural changes induced by addition of WO3 and MoO3. Despite the potential of WO3 and MoO3 to induce polaronic (electronic) conductivity, these glasses are purely ionic conductors. The increase in lithium-ion conductivity is approximately 5 and 4 orders of magnitude with addition of up to ≈40 mol % WO3 and MoO3, respectively. A detailed structural analysis shows that the increase in the mobility of Li+ ions is related to a strong facilitating effect of tungstate and molybdate units in the glass network. Moreover, this study also discusses similarities and differences in the dynamics of lithium and sodium ions in phosphate glasses containing WO3 and MoO3, and shows that the addition of WO3 can enhance the cathode performance of these glasses in both lithium-ion and sodium-ion batteries.

Abstract Image

通过添加过渡金属氧化物以增强磷酸盐玻璃中的离子电导率来剪裁玻璃网络结构
在开发用于固态电池的氧化玻璃电解质和电极时,高离子电导率是一个终极挑战。增加这些材料中离子电导率的一种方法是通过添加过渡金属氧化物来增加离子的迁移率。在这项研究中,我们报道了由于添加WO3和MoO3引起的结构变化而显著增强了锂离子的电导率。尽管WO3和MoO3具有诱导极化(电子)导电性的潜力,但这些玻璃是纯离子导体。当添加高达约40 mol %的WO3和MoO3时,锂离子的电导率分别提高了约5和4个数量级。详细的结构分析表明,Li+离子迁移率的增加与玻璃网络中钨酸盐和钼酸盐单元的强促进作用有关。此外,本研究还讨论了含WO3和MoO3的磷酸盐玻璃中锂离子和钠离子动力学的异同,表明在锂离子和钠离子电池中,加入WO3都可以提高这些玻璃的阴极性能。
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来源期刊
Inorganic Chemistry
Inorganic Chemistry 化学-无机化学与核化学
CiteScore
7.60
自引率
13.00%
发文量
1960
审稿时长
1.9 months
期刊介绍: Inorganic Chemistry publishes fundamental studies in all phases of inorganic chemistry. Coverage includes experimental and theoretical reports on quantitative studies of structure and thermodynamics, kinetics, mechanisms of inorganic reactions, bioinorganic chemistry, and relevant aspects of organometallic chemistry, solid-state phenomena, and chemical bonding theory. Emphasis is placed on the synthesis, structure, thermodynamics, reactivity, spectroscopy, and bonding properties of significant new and known compounds.
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