Structural changes in a commercial lithium-ion battery during electrochemical cycling: An in situ neutron diffraction study

The structural response to electrochemical cycling of the components within a commercial Li-ion battery (LiCoO2 cathode, graphite anode) is shown through in situ neutron diffraction. Lithuim insertion and extraction is observed in both the cathode and anode. In particular, reversible Li incorporatio...

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發表在:Journal of Power Sources
主要作者: 2-s2.0-77956481626
格式: Article
語言:English
出版: 2010
在線閱讀:https://www.scopus.com/inward/record.uri?eid=2-s2.0-77956481626&doi=10.1016%2fj.jpowsour.2010.06.114&partnerID=40&md5=8130a164d9b682169d1d46885dcc9dcc
id Sharma N.; Peterson V.K.; Elcombe M.M.; Avdeev M.; Studer A.J.; Blagojevic N.; Yusoff R.; Kamarulzaman N.
spelling Sharma N.; Peterson V.K.; Elcombe M.M.; Avdeev M.; Studer A.J.; Blagojevic N.; Yusoff R.; Kamarulzaman N.
2-s2.0-77956481626
Structural changes in a commercial lithium-ion battery during electrochemical cycling: An in situ neutron diffraction study
2010
Journal of Power Sources
195
24
10.1016/j.jpowsour.2010.06.114
https://www.scopus.com/inward/record.uri?eid=2-s2.0-77956481626&doi=10.1016%2fj.jpowsour.2010.06.114&partnerID=40&md5=8130a164d9b682169d1d46885dcc9dcc
The structural response to electrochemical cycling of the components within a commercial Li-ion battery (LiCoO2 cathode, graphite anode) is shown through in situ neutron diffraction. Lithuim insertion and extraction is observed in both the cathode and anode. In particular, reversible Li incorporation into both layered and spinel-type LiCoO2 phases that comprise the cathode is shown and each of these components features several phase transitions attributed to Li content and correlated with the state-of-charge of the battery. At the anode, a constant cell voltage correlates with a stable lithiated graphite phase. Transformation to de-lithiated graphite at the discharged state is characterised by a sharp decrease in both structural cell parameters and cell voltage. In the charged state, a two-phase region exists and is composed of the lithiated graphite phase and about 64% LiC 6. It is postulated that trapping Li in the solidelectrolyte interface layer results in minimal structural changes to the lithiated graphite anode across the constant cell voltage regions of the electrochemical cycle. © 2010 Elsevier B.V. All rights reserved.

3787753
English
Article

author 2-s2.0-77956481626
spellingShingle 2-s2.0-77956481626
Structural changes in a commercial lithium-ion battery during electrochemical cycling: An in situ neutron diffraction study
author_facet 2-s2.0-77956481626
author_sort 2-s2.0-77956481626
title Structural changes in a commercial lithium-ion battery during electrochemical cycling: An in situ neutron diffraction study
title_short Structural changes in a commercial lithium-ion battery during electrochemical cycling: An in situ neutron diffraction study
title_full Structural changes in a commercial lithium-ion battery during electrochemical cycling: An in situ neutron diffraction study
title_fullStr Structural changes in a commercial lithium-ion battery during electrochemical cycling: An in situ neutron diffraction study
title_full_unstemmed Structural changes in a commercial lithium-ion battery during electrochemical cycling: An in situ neutron diffraction study
title_sort Structural changes in a commercial lithium-ion battery during electrochemical cycling: An in situ neutron diffraction study
publishDate 2010
container_title Journal of Power Sources
container_volume 195
container_issue 24
doi_str_mv 10.1016/j.jpowsour.2010.06.114
url https://www.scopus.com/inward/record.uri?eid=2-s2.0-77956481626&doi=10.1016%2fj.jpowsour.2010.06.114&partnerID=40&md5=8130a164d9b682169d1d46885dcc9dcc
description The structural response to electrochemical cycling of the components within a commercial Li-ion battery (LiCoO2 cathode, graphite anode) is shown through in situ neutron diffraction. Lithuim insertion and extraction is observed in both the cathode and anode. In particular, reversible Li incorporation into both layered and spinel-type LiCoO2 phases that comprise the cathode is shown and each of these components features several phase transitions attributed to Li content and correlated with the state-of-charge of the battery. At the anode, a constant cell voltage correlates with a stable lithiated graphite phase. Transformation to de-lithiated graphite at the discharged state is characterised by a sharp decrease in both structural cell parameters and cell voltage. In the charged state, a two-phase region exists and is composed of the lithiated graphite phase and about 64% LiC 6. It is postulated that trapping Li in the solidelectrolyte interface layer results in minimal structural changes to the lithiated graphite anode across the constant cell voltage regions of the electrochemical cycle. © 2010 Elsevier B.V. All rights reserved.
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language English
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