Simultaneous in Situ X‑ray Absorption Spectroscopy and X‑ray Diffraction Studies on Battery Materials: The Case of Fe0.5TiOPO4

Following the reaction mechanisms of materials for Li-ion batteries under in situ conditions can provide vital new clues in the development of better battery materials. A new in situ cell was developed for such a purpose which allows an almost simultaneous measurement of XRD (X-ray diffraction) and...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of physical chemistry. C 2015-02
Hauptverfasser: Bleith, Peter, van Beek, Wouter, Kaiser, Hermann, Novák, Petr, Villevieille, Claire
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page
container_issue
container_start_page
container_title Journal of physical chemistry. C
container_volume
creator Bleith, Peter
van Beek, Wouter
Kaiser, Hermann
Novák, Petr
Villevieille, Claire
description Following the reaction mechanisms of materials for Li-ion batteries under in situ conditions can provide vital new clues in the development of better battery materials. A new in situ cell was developed for such a purpose which allows an almost simultaneous measurement of XRD (X-ray diffraction) and XAS (X-ray absorption spectroscopy) at energies as low as the Ti K-edge. Change from one method to the other was possible in less than a minute at the Swiss–Norwegian Beamline (SNBL). Using this cell with its flexibility in terms of windows, it was proven that the reaction mechanism of iron titanium oxyphosphate (Fe0.5TiOPO4) upon lithiation and delithiation consists of a combined insertion–conversion reaction with the mostly reversible reduction of Ti4+ to Ti2+ and Fe2+ to Fe0.
doi_str_mv 10.1021/jp511042x
format Article
fullrecord <record><control><sourceid>acs</sourceid><recordid>TN_cdi_acs_journals_10_1021_jp511042x</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>b543156226</sourcerecordid><originalsourceid>FETCH-LOGICAL-a251t-1100199c83958153b3f1c2f5fd06cd5ebcb436b80cf6bd66f818a17a11f050013</originalsourceid><addsrcrecordid>eNo9UE1LxDAUDKLgunrwH-TisWte0_TD27ruqrBSYSt4K2maYMralCYFexP_gX_RX2JkpacZ3pv3hhmELoEsgIRw3XQMgEThxxGaQUbDIIkYO554lJyiM2sbQhglQGfoa6ffh73jrTSDxbrFO-0G_Prz-d3zES8ra_rOaePnnRSuN1aYbsS8rSfNnVaq5-IgckOtpcWe3nLnZD_iJ-5B8729wcWbxCtuJTYKbyRZsELnz3l0jk6U38uLf5yjl826WD0E2_z-cbXcBjxk4AIfi0CWiZRmLAVGK6pAhIqpmsSiZrISVUTjKiVCxVUdxyqFlEPCARRh_pTO0dXhLxe2bMzQt96tBFL-FVdOxdFfH2Riig</addsrcrecordid><sourcetype>Publisher</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Simultaneous in Situ X‑ray Absorption Spectroscopy and X‑ray Diffraction Studies on Battery Materials: The Case of Fe0.5TiOPO4</title><source>American Chemical Society Journals</source><creator>Bleith, Peter ; van Beek, Wouter ; Kaiser, Hermann ; Novák, Petr ; Villevieille, Claire</creator><creatorcontrib>Bleith, Peter ; van Beek, Wouter ; Kaiser, Hermann ; Novák, Petr ; Villevieille, Claire</creatorcontrib><description>Following the reaction mechanisms of materials for Li-ion batteries under in situ conditions can provide vital new clues in the development of better battery materials. A new in situ cell was developed for such a purpose which allows an almost simultaneous measurement of XRD (X-ray diffraction) and XAS (X-ray absorption spectroscopy) at energies as low as the Ti K-edge. Change from one method to the other was possible in less than a minute at the Swiss–Norwegian Beamline (SNBL). Using this cell with its flexibility in terms of windows, it was proven that the reaction mechanism of iron titanium oxyphosphate (Fe0.5TiOPO4) upon lithiation and delithiation consists of a combined insertion–conversion reaction with the mostly reversible reduction of Ti4+ to Ti2+ and Fe2+ to Fe0.</description><identifier>ISSN: 1932-7447</identifier><identifier>EISSN: 1932-7455</identifier><identifier>DOI: 10.1021/jp511042x</identifier><language>eng</language><publisher>American Chemical Society</publisher><ispartof>Journal of physical chemistry. C, 2015-02</ispartof><rights>Copyright © American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/jp511042x$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/jp511042x$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,780,784,27076,27924,27925,56738,56788</link.rule.ids></links><search><creatorcontrib>Bleith, Peter</creatorcontrib><creatorcontrib>van Beek, Wouter</creatorcontrib><creatorcontrib>Kaiser, Hermann</creatorcontrib><creatorcontrib>Novák, Petr</creatorcontrib><creatorcontrib>Villevieille, Claire</creatorcontrib><title>Simultaneous in Situ X‑ray Absorption Spectroscopy and X‑ray Diffraction Studies on Battery Materials: The Case of Fe0.5TiOPO4</title><title>Journal of physical chemistry. C</title><addtitle>J. Phys. Chem. C</addtitle><description>Following the reaction mechanisms of materials for Li-ion batteries under in situ conditions can provide vital new clues in the development of better battery materials. A new in situ cell was developed for such a purpose which allows an almost simultaneous measurement of XRD (X-ray diffraction) and XAS (X-ray absorption spectroscopy) at energies as low as the Ti K-edge. Change from one method to the other was possible in less than a minute at the Swiss–Norwegian Beamline (SNBL). Using this cell with its flexibility in terms of windows, it was proven that the reaction mechanism of iron titanium oxyphosphate (Fe0.5TiOPO4) upon lithiation and delithiation consists of a combined insertion–conversion reaction with the mostly reversible reduction of Ti4+ to Ti2+ and Fe2+ to Fe0.</description><issn>1932-7447</issn><issn>1932-7455</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNo9UE1LxDAUDKLgunrwH-TisWte0_TD27ruqrBSYSt4K2maYMralCYFexP_gX_RX2JkpacZ3pv3hhmELoEsgIRw3XQMgEThxxGaQUbDIIkYO554lJyiM2sbQhglQGfoa6ffh73jrTSDxbrFO-0G_Prz-d3zES8ra_rOaePnnRSuN1aYbsS8rSfNnVaq5-IgckOtpcWe3nLnZD_iJ-5B8729wcWbxCtuJTYKbyRZsELnz3l0jk6U38uLf5yjl826WD0E2_z-cbXcBjxk4AIfi0CWiZRmLAVGK6pAhIqpmsSiZrISVUTjKiVCxVUdxyqFlEPCARRh_pTO0dXhLxe2bMzQt96tBFL-FVdOxdFfH2Riig</recordid><startdate>20150219</startdate><enddate>20150219</enddate><creator>Bleith, Peter</creator><creator>van Beek, Wouter</creator><creator>Kaiser, Hermann</creator><creator>Novák, Petr</creator><creator>Villevieille, Claire</creator><general>American Chemical Society</general><scope/></search><sort><creationdate>20150219</creationdate><title>Simultaneous in Situ X‑ray Absorption Spectroscopy and X‑ray Diffraction Studies on Battery Materials: The Case of Fe0.5TiOPO4</title><author>Bleith, Peter ; van Beek, Wouter ; Kaiser, Hermann ; Novák, Petr ; Villevieille, Claire</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a251t-1100199c83958153b3f1c2f5fd06cd5ebcb436b80cf6bd66f818a17a11f050013</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bleith, Peter</creatorcontrib><creatorcontrib>van Beek, Wouter</creatorcontrib><creatorcontrib>Kaiser, Hermann</creatorcontrib><creatorcontrib>Novák, Petr</creatorcontrib><creatorcontrib>Villevieille, Claire</creatorcontrib><jtitle>Journal of physical chemistry. C</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bleith, Peter</au><au>van Beek, Wouter</au><au>Kaiser, Hermann</au><au>Novák, Petr</au><au>Villevieille, Claire</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Simultaneous in Situ X‑ray Absorption Spectroscopy and X‑ray Diffraction Studies on Battery Materials: The Case of Fe0.5TiOPO4</atitle><jtitle>Journal of physical chemistry. C</jtitle><addtitle>J. Phys. Chem. C</addtitle><date>2015-02-19</date><risdate>2015</risdate><issn>1932-7447</issn><eissn>1932-7455</eissn><abstract>Following the reaction mechanisms of materials for Li-ion batteries under in situ conditions can provide vital new clues in the development of better battery materials. A new in situ cell was developed for such a purpose which allows an almost simultaneous measurement of XRD (X-ray diffraction) and XAS (X-ray absorption spectroscopy) at energies as low as the Ti K-edge. Change from one method to the other was possible in less than a minute at the Swiss–Norwegian Beamline (SNBL). Using this cell with its flexibility in terms of windows, it was proven that the reaction mechanism of iron titanium oxyphosphate (Fe0.5TiOPO4) upon lithiation and delithiation consists of a combined insertion–conversion reaction with the mostly reversible reduction of Ti4+ to Ti2+ and Fe2+ to Fe0.</abstract><pub>American Chemical Society</pub><doi>10.1021/jp511042x</doi></addata></record>
fulltext fulltext
identifier ISSN: 1932-7447
ispartof Journal of physical chemistry. C, 2015-02
issn 1932-7447
1932-7455
language eng
recordid cdi_acs_journals_10_1021_jp511042x
source American Chemical Society Journals
title Simultaneous in Situ X‑ray Absorption Spectroscopy and X‑ray Diffraction Studies on Battery Materials: The Case of Fe0.5TiOPO4
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-26T22%3A36%3A11IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-acs&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Simultaneous%20in%20Situ%20X%E2%80%91ray%20Absorption%20Spectroscopy%20and%20X%E2%80%91ray%20Diffraction%20Studies%20on%20Battery%20Materials:%20The%20Case%20of%20Fe0.5TiOPO4&rft.jtitle=Journal%20of%20physical%20chemistry.%20C&rft.au=Bleith,%20Peter&rft.date=2015-02-19&rft.issn=1932-7447&rft.eissn=1932-7455&rft_id=info:doi/10.1021/jp511042x&rft_dat=%3Cacs%3Eb543156226%3C/acs%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true