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锂金属负极上固体电解质界面膜(SEI)和枝晶形成的电化学原位研究。

Electrochemical in situ investigations of SEI and dendrite formation on the lithium metal anode.

作者信息

Bieker Georg, Winter Martin, Bieker Peter

机构信息

MEET Battery Research Center, Institute of Physical Chemistry, University of Münster, Corrensstrasse 28/30, 48149 Münster, Germany.

出版信息

Phys Chem Chem Phys. 2015 Apr 14;17(14):8670-9. doi: 10.1039/c4cp05865h. Epub 2015 Mar 4.

Abstract

This comparative work studies the self-enforcing heterogeneity of lithium deposition and dissolution as the cause for dendrite formation on the lithium metal anode in various liquid organic solvent based electrolytes. In addition, the ongoing lithium corrosion, its rate and thus the passivating quality of the SEI are investigated in self-discharge measurements. The behavior of the lithium anode is characterized in two carbonate-based standard electrolytes, 1 M LiPF6 in EC/DEC (3 : 7) and 1 M LiPF6 in EC/DMC (1 : 1), and in two alternative electrolytes 1 M LiPF6 in TEGDME and 1 M LiTFSI in DMSO, which have been proposed in the literature as promising electrolytes for lithium metal batteries, more specifically for lithium/air batteries. As a result, electrolyte decomposition, SEI and dendrite formation at the lithium electrode as well as their mutual influences are understood in the development of overpotentials, surface resistances and lithium electrode surface morphologies in subsequent lithium deposition and dissolution processes. A general model of different stages of these processes could be elaborated.

摘要

这项对比研究工作探究了锂沉积和溶解的自增强异质性,这是各种基于液体有机溶剂的电解质中锂金属阳极上枝晶形成的原因。此外,在自放电测量中研究了持续的锂腐蚀、其速率以及因此形成的固体电解质界面(SEI)的钝化质量。锂阳极的行为在两种基于碳酸盐的标准电解质(1 M LiPF6溶于碳酸乙烯酯/碳酸二乙酯(3∶7)和1 M LiPF6溶于碳酸乙烯酯/碳酸二甲酯(1∶1))以及两种替代电解质(1 M LiPF6溶于四甘醇二甲醚和1 M 双三氟甲烷磺酰亚胺锂溶于二甲基亚砜)中进行了表征,这些电解质在文献中被提议作为锂金属电池,更具体地说是锂/空气电池的有前景的电解质。结果,在随后的锂沉积和溶解过程中,通过过电位、表面电阻和锂电极表面形态的发展,了解了锂电极处的电解质分解、SEI和枝晶形成以及它们之间的相互影响。可以阐述这些过程不同阶段的通用模型。

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