Revisiting Delithiated Li1.2Mn0.54Ni0.13Co0.13O2: Structural Analysis and Cathode Properties in Magnesium Rechargeable Battery Applications

Chemically-delithiated Li1.2Mn0.54Ni0.13Co0.13O2 is regarded as a potential candidate of cathode active materials for magnesium rechargeable batteries owing to its large deliverable capacity and high operation voltage compared to conventional layered transition metal oxides. Our previous study sugge...

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Main Authors: Naoya ISHIDA, Ryuta NISHIGAMI, Masaki MATSUI, Toshihiko MANDAI, Kiyoshi KANAMURA, Naoto KITAMURA, Yasushi IDEMOTO
Format: Article
Language:English
Published: The Electrochemical Society of Japan 2021-07-01
Series:Electrochemistry
Subjects:
Online Access:https://www.jstage.jst.go.jp/article/electrochemistry/89/4/89_21-00038/_pdf/-char/en
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author Naoya ISHIDA
Ryuta NISHIGAMI
Masaki MATSUI
Toshihiko MANDAI
Kiyoshi KANAMURA
Naoto KITAMURA
Yasushi IDEMOTO
author_facet Naoya ISHIDA
Ryuta NISHIGAMI
Masaki MATSUI
Toshihiko MANDAI
Kiyoshi KANAMURA
Naoto KITAMURA
Yasushi IDEMOTO
author_sort Naoya ISHIDA
collection DOAJ
description Chemically-delithiated Li1.2Mn0.54Ni0.13Co0.13O2 is regarded as a potential candidate of cathode active materials for magnesium rechargeable batteries owing to its large deliverable capacity and high operation voltage compared to conventional layered transition metal oxides. Our previous study suggested its chemical composition as Li0.13Mn0.54Ni0.13Co0.13O2−δ by X-ray diffraction combined with XAFS analysis. We herein re-analyzed the substantial composition and crystal structure by employing titration technique and combination of neutron and synchrotron X-ray diffractions. Two topotactic phases both belonging to the space group of R3m were strongly suggested by Rietveld analysis, and the chemical formula was subsequently re-defined as Li0.17Mn0.72Ni0.18Co0.18O2 where oxygen defects were filled by a rearrangement from C2/m structure. Although the battery performance of that active material was poor in the previous study, the discharge capacity greater than 400 mAh g−1, ca. 95 % of the theoretical capacity, was achieved by using certain anodically stable electrolytes and specific cell configuration. This result strongly implies that the R3m structure is particularly suitable as a host material for Mg2+ intercalation.
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spelling doaj.art-ca23bb18289c4135a7aab90d41f4cc992023-01-02T17:19:29ZengThe Electrochemical Society of JapanElectrochemistry2186-24512021-07-0189432933310.5796/electrochemistry.21-00038electrochemistryRevisiting Delithiated Li1.2Mn0.54Ni0.13Co0.13O2: Structural Analysis and Cathode Properties in Magnesium Rechargeable Battery ApplicationsNaoya ISHIDA0Ryuta NISHIGAMI1Masaki MATSUI2Toshihiko MANDAI3Kiyoshi KANAMURA4Naoto KITAMURA5Yasushi IDEMOTO6Faculty of Science & Technology, Tokyo University of ScienceFaculty of Science & Technology, Tokyo University of ScienceDepartment of Chemical Science and Engineering, Kobe UniversityCenter for Green Research on Energy and Environmental Materials, National Institute for Materials ScienceGraduate School of Urban Environmental Sciences, Tokyo Metropolitan UniversityFaculty of Science & Technology, Tokyo University of ScienceFaculty of Science & Technology, Tokyo University of ScienceChemically-delithiated Li1.2Mn0.54Ni0.13Co0.13O2 is regarded as a potential candidate of cathode active materials for magnesium rechargeable batteries owing to its large deliverable capacity and high operation voltage compared to conventional layered transition metal oxides. Our previous study suggested its chemical composition as Li0.13Mn0.54Ni0.13Co0.13O2−δ by X-ray diffraction combined with XAFS analysis. We herein re-analyzed the substantial composition and crystal structure by employing titration technique and combination of neutron and synchrotron X-ray diffractions. Two topotactic phases both belonging to the space group of R3m were strongly suggested by Rietveld analysis, and the chemical formula was subsequently re-defined as Li0.17Mn0.72Ni0.18Co0.18O2 where oxygen defects were filled by a rearrangement from C2/m structure. Although the battery performance of that active material was poor in the previous study, the discharge capacity greater than 400 mAh g−1, ca. 95 % of the theoretical capacity, was achieved by using certain anodically stable electrolytes and specific cell configuration. This result strongly implies that the R3m structure is particularly suitable as a host material for Mg2+ intercalation.https://www.jstage.jst.go.jp/article/electrochemistry/89/4/89_21-00038/_pdf/-char/enmg rechargeable batterycathode materialcrystal structureneutron diffraction
spellingShingle Naoya ISHIDA
Ryuta NISHIGAMI
Masaki MATSUI
Toshihiko MANDAI
Kiyoshi KANAMURA
Naoto KITAMURA
Yasushi IDEMOTO
Revisiting Delithiated Li1.2Mn0.54Ni0.13Co0.13O2: Structural Analysis and Cathode Properties in Magnesium Rechargeable Battery Applications
Electrochemistry
mg rechargeable battery
cathode material
crystal structure
neutron diffraction
title Revisiting Delithiated Li1.2Mn0.54Ni0.13Co0.13O2: Structural Analysis and Cathode Properties in Magnesium Rechargeable Battery Applications
title_full Revisiting Delithiated Li1.2Mn0.54Ni0.13Co0.13O2: Structural Analysis and Cathode Properties in Magnesium Rechargeable Battery Applications
title_fullStr Revisiting Delithiated Li1.2Mn0.54Ni0.13Co0.13O2: Structural Analysis and Cathode Properties in Magnesium Rechargeable Battery Applications
title_full_unstemmed Revisiting Delithiated Li1.2Mn0.54Ni0.13Co0.13O2: Structural Analysis and Cathode Properties in Magnesium Rechargeable Battery Applications
title_short Revisiting Delithiated Li1.2Mn0.54Ni0.13Co0.13O2: Structural Analysis and Cathode Properties in Magnesium Rechargeable Battery Applications
title_sort revisiting delithiated li1 2mn0 54ni0 13co0 13o2 structural analysis and cathode properties in magnesium rechargeable battery applications
topic mg rechargeable battery
cathode material
crystal structure
neutron diffraction
url https://www.jstage.jst.go.jp/article/electrochemistry/89/4/89_21-00038/_pdf/-char/en
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