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通过室温简易表面氟化实现无枝晶碱金属阳极的可扩展方法。

A Scalable Approach for Dendrite-Free Alkali Metal Anodes via Room-Temperature Facile Surface Fluorination.

机构信息

Guangzhou Key Laboratory of Surface Chemistry of Energy Materials, New Energy Research Institute, School of Environment and Energy , South China University of Technology , Guangzhou 510006 , China.

Guangdong Engineering and Technology Research Center for Advanced Nanomaterials, School of Environment and Civil Engineering , Dongguan University of Technology , Dongguan 523808 , China.

出版信息

ACS Appl Mater Interfaces. 2019 Feb 6;11(5):4962-4968. doi: 10.1021/acsami.8b18101. Epub 2019 Jan 22.

Abstract

Alkali metals are attractive anode materials for advanced high-energy-density battery systems because of their high theoretical specific capacities as well as low electrochemical potential. However, severe dendrite growth as well as high chemical reactivity restrict their practical application in energy storage technologies. Herein, we propose a facile scalable solution-based approach to stabilize Li and Na anodes via the facile process of immersing the Li/Na metal in a nonhazardous ionic liquid 1-butyl-2,3-dimethylimidazolium tetrafluoroborate for several minutes at room temperature before battery assembly. This produces a dense and robust artificial fluoride layer, formed in situ by the reaction of the ionic liquid and Li/Na metal. As a demonstration, a homogeneous and compact LiF coating on the Li metal anode was fabricated via our method and it can effectively suppress the growth of Li dendrites and the continuous decomposition of electrolytes during cycling. As a result, the LiF-coated metallic Li anode achieves an enhanced cycling lifespan of over 700 h with low overpotential (∼22 mV) at 1 mA cm, as well as a very high Coulombic efficiency of up to 98.1% for 200 cycles at 1 mA cm. Furthermore, the successful achievements of the dendrite-free Na deposition show the versatility of room-temperature surface fluorination for potential battery applications.

摘要

碱金属因其具有高的理论比容量和低的电化学电势,是先进高能量密度电池系统有吸引力的阳极材料。然而,严重的枝晶生长和高的化学反应性限制了它们在储能技术中的实际应用。在此,我们提出了一种简便的基于溶液的方法,通过在室温下将 Li/Na 金属浸入非危险的离子液体 1-丁基-2,3-二甲基咪唑四氟硼酸盐中几分钟的简便过程来稳定 Li 和 Na 阳极。这会产生一层致密而坚固的人工氟化物层,是由离子液体和 Li/Na 金属的反应原位形成的。作为一个例子,我们的方法在 Li 金属阳极上制备了均匀且致密的 LiF 涂层,它可以有效地抑制枝晶的生长和循环过程中电解质的连续分解。结果,LiF 涂层的金属 Li 阳极在 1 mA cm 时具有超过 700 小时的增强循环寿命和低过电势(约 22 mV),以及在 1 mA cm 时高达 98.1%的非常高的库仑效率,可达 200 个循环。此外,无枝晶 Na 沉积的成功实现表明了室温表面氟化在潜在电池应用中的多功能性。

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