通过 KB11H14-2Me3NBH3 复合物电解质实现稳定的固态钾金属电池

IF 6.4 1区 化学 Q1 CHEMISTRY, INORGANIC & NUCLEAR Inorganic Chemistry Frontiers Pub Date : 2024-11-05 DOI:10.1039/D4QI02372B
Guo-Guo Zhang, Pengtao Qiu, Jia-Xin Kang, Zhiwei Lu, An-Qi Zhu, Xiaohu Yu and Xuenian Chen
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摘要

固态钾金属电池因其安全性和低成本而日益受到人们的关注,成为大规模能源储存的理想替代品。然而,这些电池通常缺乏合适的 K+ 导电固体电解质。本文报告了一种新的 KB11H14-2Me3NBH3 复合物电解质,它具有高离子电导率和对 K 金属的相对稳定性。晶体结构为单斜 P21/c 晶格。密度泛函理论(DFT)计算证实,该结构中的 K 离子扩散显著增强。在 25 ℃ 和 75 ℃ 条件下,其 K 离子电导率分别达到 2.63 × 10-6 S cm-1 和 3.25 × 10-4 S cm-1,跻身领先的 K+ 固体导体行列。此外,它还显示出与预涂 NH3B3H7 的 K 金属阳极良好的界面稳定性。使用 TiS2 阴极的电池具有长期循环稳定性。这项研究为安全的钾金属电池开辟了一组新的钾离子固态电解质。
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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Stable solid-state potassium metal batteries enabled by a KB11H14·2Me3NBH3 complex electrolyte†

Solid-state potassium metal batteries have increasingly gained attention as promising alternatives in large-scale energy storage due to their safety and low cost. However, these batteries usually suffer from a lack of suitable K+ conducting solid electrolytes. Herein, a new KB11H14·2Me3NBH3 complex electrolyte with high ionic conductivity and relative stability against K metal is reported. The crystal structure was solved as a monoclinic P21/c lattice. Density functional theory (DFT) calculations confirm significantly enhanced K-ion diffusion in the structure. High K-ion conductivities of 2.63 × 10−6 S cm−1 at 25 °C and 3.25 × 10−4 S cm−1 at 75 °C are achieved, putting it among the leading K+ solid conductors. Moreover, it shows favorable interfacial stability against the K metal anode precoated with NH3B3H7. Batteries coupling the TiS2 cathode deliver long-term cycling stability. This work provides a new group of K-ion solid-state electrolytes for safe potassium metal batteries.

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来源期刊
Inorganic Chemistry Frontiers
Inorganic Chemistry Frontiers CHEMISTRY, INORGANIC & NUCLEAR-
CiteScore
10.40
自引率
7.10%
发文量
587
审稿时长
1.2 months
期刊介绍: The international, high quality journal for interdisciplinary research between inorganic chemistry and related subjects
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