Vacancy Occupation-Driven Polymorphic Transformation in Cobalt Ditelluride for Boosted Oxygen Evolution Reaction

Transition-metal dichalcogenides (TMDs) hold great potential as an advanced electrocatalyst for oxygen evolution reaction (OER), but to date the activity of transition metal telluride catalysts are demonstrated to be poor for this reaction. In this study, we report the activation of CoTe2 for OER by...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:ACS nano 2020-06, Vol.14 (6), p.6968-6979
Hauptverfasser: Chen, Ziliang, Chen, Mao, Yan, Xiaoxiao, Jia, Huaxian, Fei, Ben, Ha, Yuan, Qing, Huilin, Yang, Hongyuan, Liu, Miao, Wu, Renbing
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 6979
container_issue 6
container_start_page 6968
container_title ACS nano
container_volume 14
creator Chen, Ziliang
Chen, Mao
Yan, Xiaoxiao
Jia, Huaxian
Fei, Ben
Ha, Yuan
Qing, Huilin
Yang, Hongyuan
Liu, Miao
Wu, Renbing
description Transition-metal dichalcogenides (TMDs) hold great potential as an advanced electrocatalyst for oxygen evolution reaction (OER), but to date the activity of transition metal telluride catalysts are demonstrated to be poor for this reaction. In this study, we report the activation of CoTe2 for OER by doping secondary anions into Te vacancies to trigger a structural transition from the hexagonal to the orthorhombic phase. The achieved orthorhombic CoTe2 with partial vacancies occupied by P-doping exhibits an exceptional OER catalytic activity with an overpotential of only 241 mV at 10 mA cm–2 and a robust stability more than 24 h. The combined experimental and theoretical studies suggest that the defective phase transformation is controllable and allows the synergism of vacancy, doping as well as the reconstructed crystallographic structure, ensuring more exposure of catalytic active sites, rapid charge transfer, and energetically favorable intermediates. This vacancy occupation-driven strategy of structural transformation can also be manipulated by S- and Se-doping, which may offer useful guidance for developing tellurides-based electrocatalyst for OER.
doi_str_mv 10.1021/acsnano.0c01456
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2408822605</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2408822605</sourcerecordid><originalsourceid>FETCH-LOGICAL-a310t-196b386af4f37bc8f875dc2f776dfaf0c8a218f3869f312ada2d282c3d1701173</originalsourceid><addsrcrecordid>eNp1kM1LAzEQxRdRsFbPXnMUZNsk203So7b1AwoVqeItTLOJpmyTNdkt7n_v9gNvnubB_N5j5iXJNcEDgikZgooOnB9ghckoZydJj4wzlmLBPk7_dE7Ok4sY1xjnXHDWS6p3UOBUixZKNRXU1rt0GuxWO_Tiy3bjQ_VlFVoGcNH4sNkTyDo08SsoazS1tS7LJthCo26P7r2PtS7Q4qf97DJmW182e8urBrUTl8mZgTLqq-PsJ28Ps-XkKZ0vHp8nd_MUMoLrlIzZKhMMzMhkfKWEETwvFDWcs8KAwUoAJcJ0yNhkhEIBtKCCqqwgHBPCs35yc8itgv9udKzlxkbV3QpO-yZKOsJCUMpw3qHDA6qCjzFoI6tgNxBaSbDcdSuP3cpjt53j9uDoFnLtm-C6V_6lfwG4uH83</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2408822605</pqid></control><display><type>article</type><title>Vacancy Occupation-Driven Polymorphic Transformation in Cobalt Ditelluride for Boosted Oxygen Evolution Reaction</title><source>ACS Publications</source><creator>Chen, Ziliang ; Chen, Mao ; Yan, Xiaoxiao ; Jia, Huaxian ; Fei, Ben ; Ha, Yuan ; Qing, Huilin ; Yang, Hongyuan ; Liu, Miao ; Wu, Renbing</creator><creatorcontrib>Chen, Ziliang ; Chen, Mao ; Yan, Xiaoxiao ; Jia, Huaxian ; Fei, Ben ; Ha, Yuan ; Qing, Huilin ; Yang, Hongyuan ; Liu, Miao ; Wu, Renbing</creatorcontrib><description>Transition-metal dichalcogenides (TMDs) hold great potential as an advanced electrocatalyst for oxygen evolution reaction (OER), but to date the activity of transition metal telluride catalysts are demonstrated to be poor for this reaction. In this study, we report the activation of CoTe2 for OER by doping secondary anions into Te vacancies to trigger a structural transition from the hexagonal to the orthorhombic phase. The achieved orthorhombic CoTe2 with partial vacancies occupied by P-doping exhibits an exceptional OER catalytic activity with an overpotential of only 241 mV at 10 mA cm–2 and a robust stability more than 24 h. The combined experimental and theoretical studies suggest that the defective phase transformation is controllable and allows the synergism of vacancy, doping as well as the reconstructed crystallographic structure, ensuring more exposure of catalytic active sites, rapid charge transfer, and energetically favorable intermediates. This vacancy occupation-driven strategy of structural transformation can also be manipulated by S- and Se-doping, which may offer useful guidance for developing tellurides-based electrocatalyst for OER.</description><identifier>ISSN: 1936-0851</identifier><identifier>EISSN: 1936-086X</identifier><identifier>DOI: 10.1021/acsnano.0c01456</identifier><language>eng</language><publisher>American Chemical Society</publisher><ispartof>ACS nano, 2020-06, Vol.14 (6), p.6968-6979</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a310t-196b386af4f37bc8f875dc2f776dfaf0c8a218f3869f312ada2d282c3d1701173</citedby><cites>FETCH-LOGICAL-a310t-196b386af4f37bc8f875dc2f776dfaf0c8a218f3869f312ada2d282c3d1701173</cites><orcidid>0000-0002-1843-9519 ; 0000-0003-2815-2797</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/acsnano.0c01456$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/acsnano.0c01456$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,780,784,2764,27075,27923,27924,56737,56787</link.rule.ids></links><search><creatorcontrib>Chen, Ziliang</creatorcontrib><creatorcontrib>Chen, Mao</creatorcontrib><creatorcontrib>Yan, Xiaoxiao</creatorcontrib><creatorcontrib>Jia, Huaxian</creatorcontrib><creatorcontrib>Fei, Ben</creatorcontrib><creatorcontrib>Ha, Yuan</creatorcontrib><creatorcontrib>Qing, Huilin</creatorcontrib><creatorcontrib>Yang, Hongyuan</creatorcontrib><creatorcontrib>Liu, Miao</creatorcontrib><creatorcontrib>Wu, Renbing</creatorcontrib><title>Vacancy Occupation-Driven Polymorphic Transformation in Cobalt Ditelluride for Boosted Oxygen Evolution Reaction</title><title>ACS nano</title><addtitle>ACS Nano</addtitle><description>Transition-metal dichalcogenides (TMDs) hold great potential as an advanced electrocatalyst for oxygen evolution reaction (OER), but to date the activity of transition metal telluride catalysts are demonstrated to be poor for this reaction. In this study, we report the activation of CoTe2 for OER by doping secondary anions into Te vacancies to trigger a structural transition from the hexagonal to the orthorhombic phase. The achieved orthorhombic CoTe2 with partial vacancies occupied by P-doping exhibits an exceptional OER catalytic activity with an overpotential of only 241 mV at 10 mA cm–2 and a robust stability more than 24 h. The combined experimental and theoretical studies suggest that the defective phase transformation is controllable and allows the synergism of vacancy, doping as well as the reconstructed crystallographic structure, ensuring more exposure of catalytic active sites, rapid charge transfer, and energetically favorable intermediates. This vacancy occupation-driven strategy of structural transformation can also be manipulated by S- and Se-doping, which may offer useful guidance for developing tellurides-based electrocatalyst for OER.</description><issn>1936-0851</issn><issn>1936-086X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp1kM1LAzEQxRdRsFbPXnMUZNsk203So7b1AwoVqeItTLOJpmyTNdkt7n_v9gNvnubB_N5j5iXJNcEDgikZgooOnB9ghckoZydJj4wzlmLBPk7_dE7Ok4sY1xjnXHDWS6p3UOBUixZKNRXU1rt0GuxWO_Tiy3bjQ_VlFVoGcNH4sNkTyDo08SsoazS1tS7LJthCo26P7r2PtS7Q4qf97DJmW182e8urBrUTl8mZgTLqq-PsJ28Ps-XkKZ0vHp8nd_MUMoLrlIzZKhMMzMhkfKWEETwvFDWcs8KAwUoAJcJ0yNhkhEIBtKCCqqwgHBPCs35yc8itgv9udKzlxkbV3QpO-yZKOsJCUMpw3qHDA6qCjzFoI6tgNxBaSbDcdSuP3cpjt53j9uDoFnLtm-C6V_6lfwG4uH83</recordid><startdate>20200623</startdate><enddate>20200623</enddate><creator>Chen, Ziliang</creator><creator>Chen, Mao</creator><creator>Yan, Xiaoxiao</creator><creator>Jia, Huaxian</creator><creator>Fei, Ben</creator><creator>Ha, Yuan</creator><creator>Qing, Huilin</creator><creator>Yang, Hongyuan</creator><creator>Liu, Miao</creator><creator>Wu, Renbing</creator><general>American Chemical Society</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-1843-9519</orcidid><orcidid>https://orcid.org/0000-0003-2815-2797</orcidid></search><sort><creationdate>20200623</creationdate><title>Vacancy Occupation-Driven Polymorphic Transformation in Cobalt Ditelluride for Boosted Oxygen Evolution Reaction</title><author>Chen, Ziliang ; Chen, Mao ; Yan, Xiaoxiao ; Jia, Huaxian ; Fei, Ben ; Ha, Yuan ; Qing, Huilin ; Yang, Hongyuan ; Liu, Miao ; Wu, Renbing</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a310t-196b386af4f37bc8f875dc2f776dfaf0c8a218f3869f312ada2d282c3d1701173</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chen, Ziliang</creatorcontrib><creatorcontrib>Chen, Mao</creatorcontrib><creatorcontrib>Yan, Xiaoxiao</creatorcontrib><creatorcontrib>Jia, Huaxian</creatorcontrib><creatorcontrib>Fei, Ben</creatorcontrib><creatorcontrib>Ha, Yuan</creatorcontrib><creatorcontrib>Qing, Huilin</creatorcontrib><creatorcontrib>Yang, Hongyuan</creatorcontrib><creatorcontrib>Liu, Miao</creatorcontrib><creatorcontrib>Wu, Renbing</creatorcontrib><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>ACS nano</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chen, Ziliang</au><au>Chen, Mao</au><au>Yan, Xiaoxiao</au><au>Jia, Huaxian</au><au>Fei, Ben</au><au>Ha, Yuan</au><au>Qing, Huilin</au><au>Yang, Hongyuan</au><au>Liu, Miao</au><au>Wu, Renbing</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Vacancy Occupation-Driven Polymorphic Transformation in Cobalt Ditelluride for Boosted Oxygen Evolution Reaction</atitle><jtitle>ACS nano</jtitle><addtitle>ACS Nano</addtitle><date>2020-06-23</date><risdate>2020</risdate><volume>14</volume><issue>6</issue><spage>6968</spage><epage>6979</epage><pages>6968-6979</pages><issn>1936-0851</issn><eissn>1936-086X</eissn><abstract>Transition-metal dichalcogenides (TMDs) hold great potential as an advanced electrocatalyst for oxygen evolution reaction (OER), but to date the activity of transition metal telluride catalysts are demonstrated to be poor for this reaction. In this study, we report the activation of CoTe2 for OER by doping secondary anions into Te vacancies to trigger a structural transition from the hexagonal to the orthorhombic phase. The achieved orthorhombic CoTe2 with partial vacancies occupied by P-doping exhibits an exceptional OER catalytic activity with an overpotential of only 241 mV at 10 mA cm–2 and a robust stability more than 24 h. The combined experimental and theoretical studies suggest that the defective phase transformation is controllable and allows the synergism of vacancy, doping as well as the reconstructed crystallographic structure, ensuring more exposure of catalytic active sites, rapid charge transfer, and energetically favorable intermediates. This vacancy occupation-driven strategy of structural transformation can also be manipulated by S- and Se-doping, which may offer useful guidance for developing tellurides-based electrocatalyst for OER.</abstract><pub>American Chemical Society</pub><doi>10.1021/acsnano.0c01456</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0002-1843-9519</orcidid><orcidid>https://orcid.org/0000-0003-2815-2797</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 1936-0851
ispartof ACS nano, 2020-06, Vol.14 (6), p.6968-6979
issn 1936-0851
1936-086X
language eng
recordid cdi_proquest_miscellaneous_2408822605
source ACS Publications
title Vacancy Occupation-Driven Polymorphic Transformation in Cobalt Ditelluride for Boosted Oxygen Evolution Reaction
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-09T03%3A03%3A25IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Vacancy%20Occupation-Driven%20Polymorphic%20Transformation%20in%20Cobalt%20Ditelluride%20for%20Boosted%20Oxygen%20Evolution%20Reaction&rft.jtitle=ACS%20nano&rft.au=Chen,%20Ziliang&rft.date=2020-06-23&rft.volume=14&rft.issue=6&rft.spage=6968&rft.epage=6979&rft.pages=6968-6979&rft.issn=1936-0851&rft.eissn=1936-086X&rft_id=info:doi/10.1021/acsnano.0c01456&rft_dat=%3Cproquest_cross%3E2408822605%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2408822605&rft_id=info:pmid/&rfr_iscdi=true