纳米尺度
介观物理学
阳极
钝化
电解质
材料科学
透射电子显微镜
相间
扫描透射电子显微镜
电池(电)
扫描电子显微镜
纳米技术
化学工程
化学物理
化学
电极
复合材料
图层(电子)
物理
物理化学
生物
遗传学
功率(物理)
工程类
量子力学
作者
William Huang,Hansen Wang,David Boyle,Yuzhang Li,Yi Cui
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2020-03-16
卷期号:5 (4): 1128-1135
被引量:280
标识
DOI:10.1021/acsenergylett.0c00194
摘要
The stability of lithium batteries is tied to the physicochemical properties of the solid-electrolyte interphase (SEI). Owing to the difficulty in characterizing this sensitive interphase, the nanoscale distribution of SEI components is poorly understood. Here, we use cryogenic scanning transmission electron microscopy (cryo-STEM) to map the spatial distribution of SEI components across the metallic Li anode. We reveal that LiF, an SEI component widely believed to play an important role in battery passivation, is absent within the compact SEI film (∼15 nm); instead, LiF particles (100–400 nm) precipitate across the electrode surface. We term this larger length scale as the indirect SEI regime. On the basis of these observations, we conclude that LiF cannot be a dominant contribution to anode passivation nor does it influence Li+ transport across the compact SEI film. We refine the traditional SEI structure derived from ensemble-averaged characterizations and nuance the role of SEI components on battery performance.
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