Published October 2019 | Version v1
Journal article

In-situ scanning electron microscope observation of electrode reactions related to battery material

  • 1. Department of Applied Chemistry, Graduate School of Engineering, Osaka University, 2-1 Yamada-oka, Suita, Osaka, 565-0871 (Japan)

Description

Scanning electron microscopy (SEM) for the electrode reaction in next-generation battery with ionic liquid (IL) electrolyte, which has both high stability under vacuum and an antistatic nature, is applied to the binder-free high capacity Si anode to observe the morphology change of the Si nanoparticle aggregate active material at different potentials during charge-discharge processes. In the IL electrolyte, 1-ethyl-3-methylimidazolium bis(fluoromethylsulfonyl)amide ([C2mim][FSA]) with 1.0 M lithium bis(trifluoromethanesulfonyl)amide (Li[TFSA]), the morphology greatly varied at the plateau observed at 0.200 to 0.070 V (vs. Li(I)/Li) in the charge-discharge curve during the first cycle, suggesting that phase transition of a-Si to c-Li13Si4 is a potential problematic process. After the first cycle, the lithiation process initiated at more positive potential. Similar behavior was also recognized in the Li[TFSA]‒tetraglyme solvate IL electrolyte in a 1:1 molar ratio ([Li(G4)][TFSA]).

Additional details

Identifiers

DOI
10.1016/j.electacta.2019.06.165;
PII
S0013468619313088;

Publishing Information

Journal Title
Electrochimica Acta
Journal Volume
319
Journal Page Range
p. 158-163
ISSN
0013-4686
CODEN
ELCAAV

INIS

Country of Publication
United Kingdom
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
55081062
Subject category
S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY;
Descriptors DEI
AMIDES; ANODES; ELECTROLYTES; MOLTEN SALTS; NANOPARTICLES; PHASE TRANSFORMATIONS; SCANNING ELECTRON MICROSCOPY; STABILITY
Descriptors DEC
ELECTRODES; ELECTRON MICROSCOPY; MICROSCOPY; ORGANIC COMPOUNDS; ORGANIC NITROGEN COMPOUNDS; PARTICLES; SALTS

Optional Information

Copyright
Copyright (c) 2019 Published by Elsevier Ltd.