Li+‐Ion Extraction/Insertion of Ni‐Rich Li1+x(NiyCozMnz)wO2 (0.005<x<0.03; y:z=8:1, w≈1) Electrodes: In Situ XRD and Raman Spectroscopy Study

We present the results of our in situ X‐ray diffraction (XRD) and Raman spectroscopy measurements for the first Li‐ion extraction/insertion (charge/discharge) processes of nickel‐rich Li1+x(NiyCozMnz)wO2 (0.005

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Veröffentlicht in:ChemElectroChem 2015-10, Vol.2 (10), p.1479-1486
Hauptverfasser: Ghanty, Chandan, Markovsky, Boris, Erickson, Evan M., Talianker, Michael, Haik, Ortal, Tal‐Yossef, Yosef, Mor, Albert, Aurbach, Doron, Lampert, Jordan, Volkov, Aleksei, Shin, Ji‐Yong, Garsuch, Arnd, Chesneau, Frederick Francois, Erk, Christoph
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container_end_page 1486
container_issue 10
container_start_page 1479
container_title ChemElectroChem
container_volume 2
creator Ghanty, Chandan
Markovsky, Boris
Erickson, Evan M.
Talianker, Michael
Haik, Ortal
Tal‐Yossef, Yosef
Mor, Albert
Aurbach, Doron
Lampert, Jordan
Volkov, Aleksei
Shin, Ji‐Yong
Garsuch, Arnd
Chesneau, Frederick Francois
Erk, Christoph
description We present the results of our in situ X‐ray diffraction (XRD) and Raman spectroscopy measurements for the first Li‐ion extraction/insertion (charge/discharge) processes of nickel‐rich Li1+x(NiyCozMnz)wO2 (0.005
doi_str_mv 10.1002/celc.201500160
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These cells were of a special design that provide in situ (at‐work) measurements during electrochemical polarization and can be used for regular cycling tests of practical Li‐battery electrodes. By using XRD measurements, it was established that, upon Li+ extraction, these cathode materials demonstrate structural transformations of the hexagonal phase (space group R‐3m) H1 to another hexagonal phase H2 (with a lower Li‐ion content in the lattice) and to domains comprising both of these two phases, coexisting at potentials E≈4.2–4.3 V. The above phases differ by the a and c lattice constants, which is in agreement with literature results. Evolution of the lattice constants with the electrode potential upon charge/discharge is shown to be in correlation with the differential capacity dQ/dE versus E plots and with some Raman parameters calculated from complementary in situ studies of these cathode materials by Raman spectroscopy. Let's shine some light on the subject! In situ X‐ray diffraction and in situ Raman spectroscopy are used to monitor phase changes during charge/discharge of a nickel‐rich cathode layered material for lithium‐ion batteries by using modified electrochemical cells.</description><identifier>ISSN: 2196-0216</identifier><identifier>EISSN: 2196-0216</identifier><identifier>DOI: 10.1002/celc.201500160</identifier><language>eng</language><subject>in situ studies ; Li+ extraction/insertion ; Ni-rich cathodes ; Raman spectroscopy ; X-ray diffraction</subject><ispartof>ChemElectroChem, 2015-10, Vol.2 (10), p.1479-1486</ispartof><rights>2015 WILEY‐VCH Verlag GmbH &amp; Co. 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These cells were of a special design that provide in situ (at‐work) measurements during electrochemical polarization and can be used for regular cycling tests of practical Li‐battery electrodes. By using XRD measurements, it was established that, upon Li+ extraction, these cathode materials demonstrate structural transformations of the hexagonal phase (space group R‐3m) H1 to another hexagonal phase H2 (with a lower Li‐ion content in the lattice) and to domains comprising both of these two phases, coexisting at potentials E≈4.2–4.3 V. The above phases differ by the a and c lattice constants, which is in agreement with literature results. Evolution of the lattice constants with the electrode potential upon charge/discharge is shown to be in correlation with the differential capacity dQ/dE versus E plots and with some Raman parameters calculated from complementary in situ studies of these cathode materials by Raman spectroscopy. Let's shine some light on the subject! 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These cells were of a special design that provide in situ (at‐work) measurements during electrochemical polarization and can be used for regular cycling tests of practical Li‐battery electrodes. By using XRD measurements, it was established that, upon Li+ extraction, these cathode materials demonstrate structural transformations of the hexagonal phase (space group R‐3m) H1 to another hexagonal phase H2 (with a lower Li‐ion content in the lattice) and to domains comprising both of these two phases, coexisting at potentials E≈4.2–4.3 V. The above phases differ by the a and c lattice constants, which is in agreement with literature results. Evolution of the lattice constants with the electrode potential upon charge/discharge is shown to be in correlation with the differential capacity dQ/dE versus E plots and with some Raman parameters calculated from complementary in situ studies of these cathode materials by Raman spectroscopy. Let's shine some light on the subject! In situ X‐ray diffraction and in situ Raman spectroscopy are used to monitor phase changes during charge/discharge of a nickel‐rich cathode layered material for lithium‐ion batteries by using modified electrochemical cells.</abstract><doi>10.1002/celc.201500160</doi><tpages>8</tpages></addata></record>
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subjects in situ studies
Li+ extraction/insertion
Ni-rich cathodes
Raman spectroscopy
X-ray diffraction
title Li+‐Ion Extraction/Insertion of Ni‐Rich Li1+x(NiyCozMnz)wO2 (0.005<x<0.03; y:z=8:1, w≈1) Electrodes: In Situ XRD and Raman Spectroscopy Study
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