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用于提高锂硫电池中硫利用率的锆基金属有机框架中的锂化缺陷位点

Lithiated Defect Sites in Zr Metal-Organic Framework for Enhanced Sulfur Utilization in Li-S Batteries.

作者信息

Baumann Avery E, Burns David A, Díaz José C, Thoi V Sara

机构信息

Department of Chemistry , Johns Hopkins University , Baltimore , Maryland 21218 , United States.

出版信息

ACS Appl Mater Interfaces. 2019 Jan 16;11(2):2159-2167. doi: 10.1021/acsami.8b19034. Epub 2019 Jan 7.

DOI:10.1021/acsami.8b19034
PMID:30576597
Abstract

Lithium sulfur (Li-S) battery technology is one of the most promising candidates for next-generation energy storage devices; however, it is still hindered by limited capacity yield and poor long-term stability. The complexity of these devices has hindered efforts to study electrochemical determinants of battery performance, impeding advancement of the field. Due to the ease of functionalization, metal-organic frameworks (MOFs) are unique platforms to explore such reactions, where integration of defects into the crystalline structure provides a convenient method for introducing synthetic handles. In Zr-based MOFs such as UiO-66, the engineered defect sites contain acidic protons that can be replaced with lithium ions, transforming defected MOFs into a range of materials with tunable lithium content. Our results demonstrate the capability of this facile lithiation procedure to create novel cathode additives and evaluate their influence on Li-S battery performance. By improving ionic conductivity and dispersion of sulfur species, lithiated MOFs enhance both sulfur utilization and capacity retention at a variety of cycling rates compared to the as-synthesized MOFs. Our general synthetic strategy has the potential to be applied to technologies beyond MOFs, including polymeric and inorganic materials. Ultimately, we illustrate that defected MOFs can be used to systematically control lithiation, currently unprecedented in conventional inorganic materials, and provide a window to examine heterogeneous reactions relevant to energy conversion and storage.

摘要

锂硫(Li-S)电池技术是下一代储能设备最有前景的候选技术之一;然而,它仍然受到容量产量有限和长期稳定性差的阻碍。这些设备的复杂性阻碍了对电池性能电化学决定因素的研究,阻碍了该领域的发展。由于功能化的便利性,金属有机框架(MOF)是探索此类反应的独特平台,将缺陷整合到晶体结构中为引入合成手柄提供了一种便捷方法。在基于锆的MOF(如UiO-66)中,工程缺陷位点含有可被锂离子取代的酸性质子,从而将有缺陷的MOF转化为一系列锂含量可调的材料。我们的结果证明了这种简便的锂化过程能够创建新型阴极添加剂并评估它们对Li-S电池性能的影响。与合成的MOF相比,锂化的MOF通过提高离子电导率和硫物种的分散性,在各种循环速率下都提高了硫利用率和容量保持率。我们的通用合成策略有可能应用于MOF以外的技术,包括聚合物和无机材料。最终,我们表明有缺陷的MOF可用于系统地控制锂化,这在传统无机材料中目前是前所未有的,并为研究与能量转换和存储相关的异质反应提供了一个窗口。

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