Detrimental MnPOF and MnF formation on LiMnO in the 3 V region
In this work, we studied the electrochemistry of LMO using thin-film electrodes in LiClO 4 and LiPF 6 based electrolyte solutions. The thin-film system allows the removal of all passive components, leaving only the LMO with a single well-defined electrode/electrolyte interface, making it an ideal sy...
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Veröffentlicht in: | Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2021-10, Vol.9 (4), p.23256-23268 |
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creator | De Taeye, Louis L Vereecken, Philippe M |
description | In this work, we studied the electrochemistry of LMO using thin-film electrodes in LiClO
4
and LiPF
6
based electrolyte solutions. The thin-film system allows the removal of all passive components, leaving only the LMO with a single well-defined electrode/electrolyte interface, making it an ideal system to study interactions at this interface. We observed a peculiar decomposition reaction when using a LiPF
6
salt based electrolyte solution, as soon as the LMO electrode was discharged below 3 V. This decomposition reaction led to the formation of a highly ionically resistive interphase layer, greatly affecting the insertion kinetics into the active material. This was in stark contrast to the LiClO
4
based electrolyte solutions, which showed ideal insertion behaviour. Through the combination of elastic recoil detection analysis (ERDA) and X-ray photoelectron spectroscopy (XPS) we determined that the reaction stems from a direct interaction between the LiPF
6
salt and tetragonal Li
2
Mn
2
O
4
.
The 3 V region of LMO is inhibited when using LiPF
6
based electrolytes, due to the formation of a LiF/MnF
2
decomposition layer. This layer is formed by direct interaction between LiPF
6
and Li
2
Mn
2
O
4
, as demonstrated using a thin-film model electrode. |
doi_str_mv | 10.1039/d1ta06227a |
format | Article |
fullrecord | <record><control><sourceid>rsc</sourceid><recordid>TN_cdi_rsc_primary_d1ta06227a</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>d1ta06227a</sourcerecordid><originalsourceid>FETCH-rsc_primary_d1ta06227a3</originalsourceid><addsrcrecordid>eNpjYBAyNNAzNDC21E8xLEk0MDMyMk9kYuA0MjA10DU3sTRjgbMtLDgYeIuLswyAwMLAwMzSkpPBziW1pCgzNzWvJDFHwTcvwN9NITEvBchyU0jLL8pNLMnMz1MAIp9M3zx_hcw8hZKMVAVjhTCFotR0oBQPA2taYk5xKi-U5maQdXMNcfbQLSpOji8AGpxYVBmPcJcxIXkA77A40Q</addsrcrecordid><sourcetype>Publisher</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Detrimental MnPOF and MnF formation on LiMnO in the 3 V region</title><source>Royal Society Of Chemistry Journals 2008-</source><creator>De Taeye, Louis L ; Vereecken, Philippe M</creator><creatorcontrib>De Taeye, Louis L ; Vereecken, Philippe M</creatorcontrib><description>In this work, we studied the electrochemistry of LMO using thin-film electrodes in LiClO
4
and LiPF
6
based electrolyte solutions. The thin-film system allows the removal of all passive components, leaving only the LMO with a single well-defined electrode/electrolyte interface, making it an ideal system to study interactions at this interface. We observed a peculiar decomposition reaction when using a LiPF
6
salt based electrolyte solution, as soon as the LMO electrode was discharged below 3 V. This decomposition reaction led to the formation of a highly ionically resistive interphase layer, greatly affecting the insertion kinetics into the active material. This was in stark contrast to the LiClO
4
based electrolyte solutions, which showed ideal insertion behaviour. Through the combination of elastic recoil detection analysis (ERDA) and X-ray photoelectron spectroscopy (XPS) we determined that the reaction stems from a direct interaction between the LiPF
6
salt and tetragonal Li
2
Mn
2
O
4
.
The 3 V region of LMO is inhibited when using LiPF
6
based electrolytes, due to the formation of a LiF/MnF
2
decomposition layer. This layer is formed by direct interaction between LiPF
6
and Li
2
Mn
2
O
4
, as demonstrated using a thin-film model electrode.</description><identifier>ISSN: 2050-7488</identifier><identifier>EISSN: 2050-7496</identifier><identifier>DOI: 10.1039/d1ta06227a</identifier><ispartof>Journal of materials chemistry. A, Materials for energy and sustainability, 2021-10, Vol.9 (4), p.23256-23268</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,778,782,27913,27914</link.rule.ids></links><search><creatorcontrib>De Taeye, Louis L</creatorcontrib><creatorcontrib>Vereecken, Philippe M</creatorcontrib><title>Detrimental MnPOF and MnF formation on LiMnO in the 3 V region</title><title>Journal of materials chemistry. A, Materials for energy and sustainability</title><description>In this work, we studied the electrochemistry of LMO using thin-film electrodes in LiClO
4
and LiPF
6
based electrolyte solutions. The thin-film system allows the removal of all passive components, leaving only the LMO with a single well-defined electrode/electrolyte interface, making it an ideal system to study interactions at this interface. We observed a peculiar decomposition reaction when using a LiPF
6
salt based electrolyte solution, as soon as the LMO electrode was discharged below 3 V. This decomposition reaction led to the formation of a highly ionically resistive interphase layer, greatly affecting the insertion kinetics into the active material. This was in stark contrast to the LiClO
4
based electrolyte solutions, which showed ideal insertion behaviour. Through the combination of elastic recoil detection analysis (ERDA) and X-ray photoelectron spectroscopy (XPS) we determined that the reaction stems from a direct interaction between the LiPF
6
salt and tetragonal Li
2
Mn
2
O
4
.
The 3 V region of LMO is inhibited when using LiPF
6
based electrolytes, due to the formation of a LiF/MnF
2
decomposition layer. This layer is formed by direct interaction between LiPF
6
and Li
2
Mn
2
O
4
, as demonstrated using a thin-film model electrode.</description><issn>2050-7488</issn><issn>2050-7496</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNpjYBAyNNAzNDC21E8xLEk0MDMyMk9kYuA0MjA10DU3sTRjgbMtLDgYeIuLswyAwMLAwMzSkpPBziW1pCgzNzWvJDFHwTcvwN9NITEvBchyU0jLL8pNLMnMz1MAIp9M3zx_hcw8hZKMVAVjhTCFotR0oBQPA2taYk5xKi-U5maQdXMNcfbQLSpOji8AGpxYVBmPcJcxIXkA77A40Q</recordid><startdate>20211019</startdate><enddate>20211019</enddate><creator>De Taeye, Louis L</creator><creator>Vereecken, Philippe M</creator><scope/></search><sort><creationdate>20211019</creationdate><title>Detrimental MnPOF and MnF formation on LiMnO in the 3 V region</title><author>De Taeye, Louis L ; Vereecken, Philippe M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-rsc_primary_d1ta06227a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><creationdate>2021</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>De Taeye, Louis L</creatorcontrib><creatorcontrib>Vereecken, Philippe M</creatorcontrib><jtitle>Journal of materials chemistry. A, Materials for energy and sustainability</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>De Taeye, Louis L</au><au>Vereecken, Philippe M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Detrimental MnPOF and MnF formation on LiMnO in the 3 V region</atitle><jtitle>Journal of materials chemistry. A, Materials for energy and sustainability</jtitle><date>2021-10-19</date><risdate>2021</risdate><volume>9</volume><issue>4</issue><spage>23256</spage><epage>23268</epage><pages>23256-23268</pages><issn>2050-7488</issn><eissn>2050-7496</eissn><abstract>In this work, we studied the electrochemistry of LMO using thin-film electrodes in LiClO
4
and LiPF
6
based electrolyte solutions. The thin-film system allows the removal of all passive components, leaving only the LMO with a single well-defined electrode/electrolyte interface, making it an ideal system to study interactions at this interface. We observed a peculiar decomposition reaction when using a LiPF
6
salt based electrolyte solution, as soon as the LMO electrode was discharged below 3 V. This decomposition reaction led to the formation of a highly ionically resistive interphase layer, greatly affecting the insertion kinetics into the active material. This was in stark contrast to the LiClO
4
based electrolyte solutions, which showed ideal insertion behaviour. Through the combination of elastic recoil detection analysis (ERDA) and X-ray photoelectron spectroscopy (XPS) we determined that the reaction stems from a direct interaction between the LiPF
6
salt and tetragonal Li
2
Mn
2
O
4
.
The 3 V region of LMO is inhibited when using LiPF
6
based electrolytes, due to the formation of a LiF/MnF
2
decomposition layer. This layer is formed by direct interaction between LiPF
6
and Li
2
Mn
2
O
4
, as demonstrated using a thin-film model electrode.</abstract><doi>10.1039/d1ta06227a</doi><tpages>13</tpages></addata></record> |
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source | Royal Society Of Chemistry Journals 2008- |
title | Detrimental MnPOF and MnF formation on LiMnO in the 3 V region |
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