Interface Sensitivity in Electron/Ion Yield X‑ray Absorption Spectroscopy: The TiO2–H2O Interface

To understand corrosion, energy storage, (electro)­catalysis, etc., obtaining chemical information on the solid–liquid interface is crucial but remains extremely challenging. Here, X-ray absorption spectroscopy (XAS) is used to study the solid–liquid interface between TiO2 and H2O. A thin film (6.7...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:The journal of physical chemistry letters 2021-10, Vol.12 (41), p.10212-10217
Hauptverfasser: van Spronsen, Matthijs A, Zhao, Xiao, Jaugstetter, Maximilian, Escudero, Carlos, Duchoň, Tomáš, Hunt, Adrian, Waluyo, Iradwikanari, Yang, Peidong, Tschulik, Kristina, Salmeron, Miquel B
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 10217
container_issue 41
container_start_page 10212
container_title The journal of physical chemistry letters
container_volume 12
creator van Spronsen, Matthijs A
Zhao, Xiao
Jaugstetter, Maximilian
Escudero, Carlos
Duchoň, Tomáš
Hunt, Adrian
Waluyo, Iradwikanari
Yang, Peidong
Tschulik, Kristina
Salmeron, Miquel B
description To understand corrosion, energy storage, (electro)­catalysis, etc., obtaining chemical information on the solid–liquid interface is crucial but remains extremely challenging. Here, X-ray absorption spectroscopy (XAS) is used to study the solid–liquid interface between TiO2 and H2O. A thin film (6.7 nm) of TiO2 is deposited on an X-ray-transparent SiN x window, acting as the working electrode in a three-electrode flow cell. The spectra are collected based on the electron emission resulting from the decay of the X-ray-induced core-hole-excited atoms, which we show is sensitive to the solid–liquid interface within a few nm. The drain currents measured at the working and counter electrodes are identical but of opposite sign. With this method, we found that the water layer next to anatase is spectroscopically similar to ice. This result highlights the potential of electron-yield XAS to obtain chemical and structural information with a high sensitivity for the species at the electrode–electrolyte interface.
doi_str_mv 10.1021/acs.jpclett.1c02115
format Article
fullrecord <record><control><sourceid>proquest_acs_j</sourceid><recordid>TN_cdi_proquest_miscellaneous_2582111952</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2582111952</sourcerecordid><originalsourceid>FETCH-LOGICAL-a273t-fb280d11b14f26cae318fd74fd73a091d50b4bb36ab00b78913ddc4a09c1a3833</originalsourceid><addsrcrecordid>eNpNkMFKAzEURYMoWKtf4CZLN9PmJTOdjLtSqi0UurCCroYkk8GUMRknqdBdf0H8w36JsS3i4vEe914uj4PQLZABEApDofxg3apGhzAAFRXIzlAPipQnOfDs_N99ia68XxMyKgjPe0jPbdBdLZTGT9p6E8ynCVtsLJ42WoXO2eHcWfxqdFPhl_3uqxNbPJbedW0w0XhqDymvXLu9x6s3jVdmSfe77xld4r_ua3RRi8brm9Puo-eH6WoySxbLx_lkvEgEzVlIakk5qQAkpDUdKaEZ8LrK0zhMkAKqjMhUSjYSkhCZ8wJYVak0WgoE44z10d2xt-3cx0b7UL4br3TTCKvdxpc045ENFBmN0eExGtmVa7fpbHysBFL-Ai0P4hFoeQLKfgDSHG6j</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2582111952</pqid></control><display><type>article</type><title>Interface Sensitivity in Electron/Ion Yield X‑ray Absorption Spectroscopy: The TiO2–H2O Interface</title><source>American Chemical Society Journals</source><creator>van Spronsen, Matthijs A ; Zhao, Xiao ; Jaugstetter, Maximilian ; Escudero, Carlos ; Duchoň, Tomáš ; Hunt, Adrian ; Waluyo, Iradwikanari ; Yang, Peidong ; Tschulik, Kristina ; Salmeron, Miquel B</creator><creatorcontrib>van Spronsen, Matthijs A ; Zhao, Xiao ; Jaugstetter, Maximilian ; Escudero, Carlos ; Duchoň, Tomáš ; Hunt, Adrian ; Waluyo, Iradwikanari ; Yang, Peidong ; Tschulik, Kristina ; Salmeron, Miquel B</creatorcontrib><description>To understand corrosion, energy storage, (electro)­catalysis, etc., obtaining chemical information on the solid–liquid interface is crucial but remains extremely challenging. Here, X-ray absorption spectroscopy (XAS) is used to study the solid–liquid interface between TiO2 and H2O. A thin film (6.7 nm) of TiO2 is deposited on an X-ray-transparent SiN x window, acting as the working electrode in a three-electrode flow cell. The spectra are collected based on the electron emission resulting from the decay of the X-ray-induced core-hole-excited atoms, which we show is sensitive to the solid–liquid interface within a few nm. The drain currents measured at the working and counter electrodes are identical but of opposite sign. With this method, we found that the water layer next to anatase is spectroscopically similar to ice. This result highlights the potential of electron-yield XAS to obtain chemical and structural information with a high sensitivity for the species at the electrode–electrolyte interface.</description><identifier>ISSN: 1948-7185</identifier><identifier>EISSN: 1948-7185</identifier><identifier>DOI: 10.1021/acs.jpclett.1c02115</identifier><language>eng</language><publisher>American Chemical Society</publisher><subject>Physical Insights into Chemistry, Catalysis, and Interfaces</subject><ispartof>The journal of physical chemistry letters, 2021-10, Vol.12 (41), p.10212-10217</ispartof><rights>2021 The Authors. Published by American Chemical Society</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><orcidid>0000-0002-5136-2816 ; 0000-0001-7637-4082 ; 0000-0002-3035-012X ; 0000-0002-4046-9722 ; 0000-0003-4799-1684 ; 0000-0002-2887-8128 ; 0000-0003-1079-664X ; 0000-0001-8716-9391</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/acs.jpclett.1c02115$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/acs.jpclett.1c02115$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,776,780,27053,27901,27902,56713,56763</link.rule.ids></links><search><creatorcontrib>van Spronsen, Matthijs A</creatorcontrib><creatorcontrib>Zhao, Xiao</creatorcontrib><creatorcontrib>Jaugstetter, Maximilian</creatorcontrib><creatorcontrib>Escudero, Carlos</creatorcontrib><creatorcontrib>Duchoň, Tomáš</creatorcontrib><creatorcontrib>Hunt, Adrian</creatorcontrib><creatorcontrib>Waluyo, Iradwikanari</creatorcontrib><creatorcontrib>Yang, Peidong</creatorcontrib><creatorcontrib>Tschulik, Kristina</creatorcontrib><creatorcontrib>Salmeron, Miquel B</creatorcontrib><title>Interface Sensitivity in Electron/Ion Yield X‑ray Absorption Spectroscopy: The TiO2–H2O Interface</title><title>The journal of physical chemistry letters</title><addtitle>J. Phys. Chem. Lett</addtitle><description>To understand corrosion, energy storage, (electro)­catalysis, etc., obtaining chemical information on the solid–liquid interface is crucial but remains extremely challenging. Here, X-ray absorption spectroscopy (XAS) is used to study the solid–liquid interface between TiO2 and H2O. A thin film (6.7 nm) of TiO2 is deposited on an X-ray-transparent SiN x window, acting as the working electrode in a three-electrode flow cell. The spectra are collected based on the electron emission resulting from the decay of the X-ray-induced core-hole-excited atoms, which we show is sensitive to the solid–liquid interface within a few nm. The drain currents measured at the working and counter electrodes are identical but of opposite sign. With this method, we found that the water layer next to anatase is spectroscopically similar to ice. This result highlights the potential of electron-yield XAS to obtain chemical and structural information with a high sensitivity for the species at the electrode–electrolyte interface.</description><subject>Physical Insights into Chemistry, Catalysis, and Interfaces</subject><issn>1948-7185</issn><issn>1948-7185</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNpNkMFKAzEURYMoWKtf4CZLN9PmJTOdjLtSqi0UurCCroYkk8GUMRknqdBdf0H8w36JsS3i4vEe914uj4PQLZABEApDofxg3apGhzAAFRXIzlAPipQnOfDs_N99ia68XxMyKgjPe0jPbdBdLZTGT9p6E8ynCVtsLJ42WoXO2eHcWfxqdFPhl_3uqxNbPJbedW0w0XhqDymvXLu9x6s3jVdmSfe77xld4r_ua3RRi8brm9Puo-eH6WoySxbLx_lkvEgEzVlIakk5qQAkpDUdKaEZ8LrK0zhMkAKqjMhUSjYSkhCZ8wJYVak0WgoE44z10d2xt-3cx0b7UL4br3TTCKvdxpc045ENFBmN0eExGtmVa7fpbHysBFL-Ai0P4hFoeQLKfgDSHG6j</recordid><startdate>20211021</startdate><enddate>20211021</enddate><creator>van Spronsen, Matthijs A</creator><creator>Zhao, Xiao</creator><creator>Jaugstetter, Maximilian</creator><creator>Escudero, Carlos</creator><creator>Duchoň, Tomáš</creator><creator>Hunt, Adrian</creator><creator>Waluyo, Iradwikanari</creator><creator>Yang, Peidong</creator><creator>Tschulik, Kristina</creator><creator>Salmeron, Miquel B</creator><general>American Chemical Society</general><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-5136-2816</orcidid><orcidid>https://orcid.org/0000-0001-7637-4082</orcidid><orcidid>https://orcid.org/0000-0002-3035-012X</orcidid><orcidid>https://orcid.org/0000-0002-4046-9722</orcidid><orcidid>https://orcid.org/0000-0003-4799-1684</orcidid><orcidid>https://orcid.org/0000-0002-2887-8128</orcidid><orcidid>https://orcid.org/0000-0003-1079-664X</orcidid><orcidid>https://orcid.org/0000-0001-8716-9391</orcidid></search><sort><creationdate>20211021</creationdate><title>Interface Sensitivity in Electron/Ion Yield X‑ray Absorption Spectroscopy: The TiO2–H2O Interface</title><author>van Spronsen, Matthijs A ; Zhao, Xiao ; Jaugstetter, Maximilian ; Escudero, Carlos ; Duchoň, Tomáš ; Hunt, Adrian ; Waluyo, Iradwikanari ; Yang, Peidong ; Tschulik, Kristina ; Salmeron, Miquel B</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a273t-fb280d11b14f26cae318fd74fd73a091d50b4bb36ab00b78913ddc4a09c1a3833</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Physical Insights into Chemistry, Catalysis, and Interfaces</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>van Spronsen, Matthijs A</creatorcontrib><creatorcontrib>Zhao, Xiao</creatorcontrib><creatorcontrib>Jaugstetter, Maximilian</creatorcontrib><creatorcontrib>Escudero, Carlos</creatorcontrib><creatorcontrib>Duchoň, Tomáš</creatorcontrib><creatorcontrib>Hunt, Adrian</creatorcontrib><creatorcontrib>Waluyo, Iradwikanari</creatorcontrib><creatorcontrib>Yang, Peidong</creatorcontrib><creatorcontrib>Tschulik, Kristina</creatorcontrib><creatorcontrib>Salmeron, Miquel B</creatorcontrib><collection>MEDLINE - Academic</collection><jtitle>The journal of physical chemistry letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>van Spronsen, Matthijs A</au><au>Zhao, Xiao</au><au>Jaugstetter, Maximilian</au><au>Escudero, Carlos</au><au>Duchoň, Tomáš</au><au>Hunt, Adrian</au><au>Waluyo, Iradwikanari</au><au>Yang, Peidong</au><au>Tschulik, Kristina</au><au>Salmeron, Miquel B</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Interface Sensitivity in Electron/Ion Yield X‑ray Absorption Spectroscopy: The TiO2–H2O Interface</atitle><jtitle>The journal of physical chemistry letters</jtitle><addtitle>J. Phys. Chem. Lett</addtitle><date>2021-10-21</date><risdate>2021</risdate><volume>12</volume><issue>41</issue><spage>10212</spage><epage>10217</epage><pages>10212-10217</pages><issn>1948-7185</issn><eissn>1948-7185</eissn><abstract>To understand corrosion, energy storage, (electro)­catalysis, etc., obtaining chemical information on the solid–liquid interface is crucial but remains extremely challenging. Here, X-ray absorption spectroscopy (XAS) is used to study the solid–liquid interface between TiO2 and H2O. A thin film (6.7 nm) of TiO2 is deposited on an X-ray-transparent SiN x window, acting as the working electrode in a three-electrode flow cell. The spectra are collected based on the electron emission resulting from the decay of the X-ray-induced core-hole-excited atoms, which we show is sensitive to the solid–liquid interface within a few nm. The drain currents measured at the working and counter electrodes are identical but of opposite sign. With this method, we found that the water layer next to anatase is spectroscopically similar to ice. This result highlights the potential of electron-yield XAS to obtain chemical and structural information with a high sensitivity for the species at the electrode–electrolyte interface.</abstract><pub>American Chemical Society</pub><doi>10.1021/acs.jpclett.1c02115</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0002-5136-2816</orcidid><orcidid>https://orcid.org/0000-0001-7637-4082</orcidid><orcidid>https://orcid.org/0000-0002-3035-012X</orcidid><orcidid>https://orcid.org/0000-0002-4046-9722</orcidid><orcidid>https://orcid.org/0000-0003-4799-1684</orcidid><orcidid>https://orcid.org/0000-0002-2887-8128</orcidid><orcidid>https://orcid.org/0000-0003-1079-664X</orcidid><orcidid>https://orcid.org/0000-0001-8716-9391</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1948-7185
ispartof The journal of physical chemistry letters, 2021-10, Vol.12 (41), p.10212-10217
issn 1948-7185
1948-7185
language eng
recordid cdi_proquest_miscellaneous_2582111952
source American Chemical Society Journals
subjects Physical Insights into Chemistry, Catalysis, and Interfaces
title Interface Sensitivity in Electron/Ion Yield X‑ray Absorption Spectroscopy: The TiO2–H2O Interface
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-01T13%3A29%3A07IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_acs_j&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Interface%20Sensitivity%20in%20Electron/Ion%20Yield%20X%E2%80%91ray%20Absorption%20Spectroscopy:%20The%20TiO2%E2%80%93H2O%20Interface&rft.jtitle=The%20journal%20of%20physical%20chemistry%20letters&rft.au=van%20Spronsen,%20Matthijs%20A&rft.date=2021-10-21&rft.volume=12&rft.issue=41&rft.spage=10212&rft.epage=10217&rft.pages=10212-10217&rft.issn=1948-7185&rft.eissn=1948-7185&rft_id=info:doi/10.1021/acs.jpclett.1c02115&rft_dat=%3Cproquest_acs_j%3E2582111952%3C/proquest_acs_j%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2582111952&rft_id=info:pmid/&rfr_iscdi=true