用于锂硫电池中有效抑制多硫化物的超薄无裂纹金属有机框架薄膜

IF 24.5 Q1 CHEMISTRY, PHYSICAL Interdisciplinary Materials Pub Date : 2024-02-05 DOI:10.1002/idm2.12143
Cheng Zhou, Chenxu Dong, Weixiao Wang, Yu Tian, Chunli Shen, Kaijian Yan, Liqiang Mai, Xu Xu
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引用次数: 0

摘要

由于具有广泛的微孔结构,金属有机框架(MOF)被广泛应用于构建改性层,起到离子筛的作用。然而,现有方法制备的改性层在 MOF 之间存在明显大于 MOF 固有孔隙尺寸的间隙。多硫化物和锂离子不可避免地会从这些间隙中渗透出来,阻碍了结构优势的充分发挥。在此,我们首次通过原子层沉积技术在分离器上形成了超薄(20 nm)、无裂纹的 MOF 膜。在分离器的基础上,通过相场模拟和原位拉曼光谱验证了不同 MOF 层的机理。结果准确证明,MOF 颗粒层可以缓解多硫化物的穿梭,但不具有均化锂离子的作用。只有孔径合适的超薄无裂纹 MOF 膜才能同时起到筛分多硫化物和锂离子的作用。因此,在 2 mA cm-2-2 mAh cm-2 的测试条件下,锂/锂对称电池在 2500 h 后的过电位仅为 18 mV。
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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An ultrathin and crack-free metal-organic framework film for effective polysulfide inhibition in lithium–sulfur batteries

Due to their extensive microporous structure, metal-organic frameworks (MOFs) find widespread application in constructing modification layers, functioning as ion sieves. However, the modification layers prepared by existing methods feature gaps between MOFs that are noticeably larger than the inherent MOF pore dimensions. Polysulfides and lithium ions unavoidably permeate through these gaps, hindering the full exploitation of the structural advantages. Herein, an ultrathin (20 nm) and crack-free MOF film is formed on the separator by atomic layer deposition for the first time. Based on the separator, the mechanism of different MOF layers has been verified by phase field simulation and in situ Raman spectroscopy. The results accurately prove that the MOF particle layer can relieve the shuttle of polysulfides, but it does not have the effect of homogenizing lithium ions. Only the ultrathin and crack-free MOF film with proper pore size can act as the ion sieve for both polysulfides and lithium ions. As a result, under the test condition of 2 mA cm−2–2 mAh cm−2, the overpotential of the Li/Li symmetric battery is only 18 mV after 2500 h. The capacity retention rate of the lithium–sulfur battery is 95.6% after 500 cycles and 80% after 1000 cycles at 2 C.

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