Manganese oxides supported on hydrogenated TiO2 nanowire array catalysts for the electrochemical oxygen evolution reaction in water electrolysis

Hydrogenated TiO 2 /MnO x nanowires (NWs) with a diameter of 50-80 nm and a length of 0.5-0.8 μm supported on carbon cloth have been successfully prepared. The entire surface of the H-TiO 2 NWs is covered uniformly by amorphous MnO x with an average thickness of 7.0 nm. The H-TiO 2 NWs are poorly ac...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: Li, Nan, Xia, Wei-Yan, Wang, Jing, Liu, Zi-Li, Li, Qing-Yu, Chen, Sheng-Zhou, Xu, Chang-Wei, Lu, Xi-Hong
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 21313
container_issue 42
container_start_page 2138
container_title
container_volume 3
creator Li, Nan
Xia, Wei-Yan
Wang, Jing
Liu, Zi-Li
Li, Qing-Yu
Chen, Sheng-Zhou
Xu, Chang-Wei
Lu, Xi-Hong
description Hydrogenated TiO 2 /MnO x nanowires (NWs) with a diameter of 50-80 nm and a length of 0.5-0.8 μm supported on carbon cloth have been successfully prepared. The entire surface of the H-TiO 2 NWs is covered uniformly by amorphous MnO x with an average thickness of 7.0 nm. The H-TiO 2 NWs are poorly active for the oxygen evolution reaction (OER) and the MnO x as a major potential feasible electrocatalyst shows a considerable activity. The onset potential shifts negatively and the current density improves not only by the enlarged surface area of the MnO x support on the H-TiO 2 NWs, but also by a synergistic effect between TiO 2 and MnO x . The presence of three manganese oxides with different valences such as MnO, Mn 2 O 3 and MnO 2 in the H-TiO 2 /MnO x NWs is apt to effect the OER due to electron transfer. The percentage of Mn 2+ increases and the percentages of Mn 3+ and Mn 4+ decrease after the test, which proves the assumption that Mn 4+ is first reduced to Mn 3+ by electron injection from H 2 O, and then Mn 3+ is further reduced to Mn 2+ when the O 2 evolution occurs during the OER in alkaline media at pH ≥ 9. Manganese oxide/hydrogenated TiO 2 core-shell nanowires exhibited enhanced electrocatalytic activity toward the oxygen evolution reaction in water electrolysis.
doi_str_mv 10.1039/c5ta04964d
format Article
fullrecord <record><control><sourceid>rsc</sourceid><recordid>TN_cdi_rsc_primary_c5ta04964d</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>c5ta04964d</sourcerecordid><originalsourceid>FETCH-LOGICAL-g240t-495a9eee8b51e4aaddb0b914ba7310e3bc7996564438af14003d16b5a001ae3d3</originalsourceid><addsrcrecordid>eNp9kM1OwzAQhC0EEhX0wh3JPEDArp00PqKKP6mol3KuNvamNUrtyHYpeQseGfN_Yy47o9F8hyXkjLNLzoS60mUCJlUlzQEZTVjJimlOh7--ro_JOMZnllUzVik1Im-P4NbgMCL1r9ZgpHHX9z4kNNQ7uhlM8Gt08JGXdjGhDpzf24AUQoCBakjQDTFF2vpA0wYpdqhT8HqDW6uhy9ghAyi--G6XbGYGBP1prKP7DA4_k8yx8ZQctdBFHH_fE_J0e7Oc3Rfzxd3D7HperCeSpUKqEhQi1k3JUQIY07BGcdnAVHCGotFTpaqyklLU0HLJmDC8akpgjAMKI07I-Rc3RL3qg91CGFZ_H8z9xX_9qjeteAfhx3Rf</addsrcrecordid><sourcetype>Enrichment Source</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Manganese oxides supported on hydrogenated TiO2 nanowire array catalysts for the electrochemical oxygen evolution reaction in water electrolysis</title><source>Royal Society Of Chemistry Journals 2008-</source><source>Alma/SFX Local Collection</source><creator>Li, Nan ; Xia, Wei-Yan ; Wang, Jing ; Liu, Zi-Li ; Li, Qing-Yu ; Chen, Sheng-Zhou ; Xu, Chang-Wei ; Lu, Xi-Hong</creator><creatorcontrib>Li, Nan ; Xia, Wei-Yan ; Wang, Jing ; Liu, Zi-Li ; Li, Qing-Yu ; Chen, Sheng-Zhou ; Xu, Chang-Wei ; Lu, Xi-Hong</creatorcontrib><description>Hydrogenated TiO 2 /MnO x nanowires (NWs) with a diameter of 50-80 nm and a length of 0.5-0.8 μm supported on carbon cloth have been successfully prepared. The entire surface of the H-TiO 2 NWs is covered uniformly by amorphous MnO x with an average thickness of 7.0 nm. The H-TiO 2 NWs are poorly active for the oxygen evolution reaction (OER) and the MnO x as a major potential feasible electrocatalyst shows a considerable activity. The onset potential shifts negatively and the current density improves not only by the enlarged surface area of the MnO x support on the H-TiO 2 NWs, but also by a synergistic effect between TiO 2 and MnO x . The presence of three manganese oxides with different valences such as MnO, Mn 2 O 3 and MnO 2 in the H-TiO 2 /MnO x NWs is apt to effect the OER due to electron transfer. The percentage of Mn 2+ increases and the percentages of Mn 3+ and Mn 4+ decrease after the test, which proves the assumption that Mn 4+ is first reduced to Mn 3+ by electron injection from H 2 O, and then Mn 3+ is further reduced to Mn 2+ when the O 2 evolution occurs during the OER in alkaline media at pH ≥ 9. Manganese oxide/hydrogenated TiO 2 core-shell nanowires exhibited enhanced electrocatalytic activity toward the oxygen evolution reaction in water electrolysis.</description><identifier>ISSN: 2050-7488</identifier><identifier>EISSN: 2050-7496</identifier><identifier>DOI: 10.1039/c5ta04964d</identifier><language>eng</language><creationdate>2015-01</creationdate><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>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Li, Nan</creatorcontrib><creatorcontrib>Xia, Wei-Yan</creatorcontrib><creatorcontrib>Wang, Jing</creatorcontrib><creatorcontrib>Liu, Zi-Li</creatorcontrib><creatorcontrib>Li, Qing-Yu</creatorcontrib><creatorcontrib>Chen, Sheng-Zhou</creatorcontrib><creatorcontrib>Xu, Chang-Wei</creatorcontrib><creatorcontrib>Lu, Xi-Hong</creatorcontrib><title>Manganese oxides supported on hydrogenated TiO2 nanowire array catalysts for the electrochemical oxygen evolution reaction in water electrolysis</title><description>Hydrogenated TiO 2 /MnO x nanowires (NWs) with a diameter of 50-80 nm and a length of 0.5-0.8 μm supported on carbon cloth have been successfully prepared. The entire surface of the H-TiO 2 NWs is covered uniformly by amorphous MnO x with an average thickness of 7.0 nm. The H-TiO 2 NWs are poorly active for the oxygen evolution reaction (OER) and the MnO x as a major potential feasible electrocatalyst shows a considerable activity. The onset potential shifts negatively and the current density improves not only by the enlarged surface area of the MnO x support on the H-TiO 2 NWs, but also by a synergistic effect between TiO 2 and MnO x . The presence of three manganese oxides with different valences such as MnO, Mn 2 O 3 and MnO 2 in the H-TiO 2 /MnO x NWs is apt to effect the OER due to electron transfer. The percentage of Mn 2+ increases and the percentages of Mn 3+ and Mn 4+ decrease after the test, which proves the assumption that Mn 4+ is first reduced to Mn 3+ by electron injection from H 2 O, and then Mn 3+ is further reduced to Mn 2+ when the O 2 evolution occurs during the OER in alkaline media at pH ≥ 9. Manganese oxide/hydrogenated TiO 2 core-shell nanowires exhibited enhanced electrocatalytic activity toward the oxygen evolution reaction in water electrolysis.</description><issn>2050-7488</issn><issn>2050-7496</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNp9kM1OwzAQhC0EEhX0wh3JPEDArp00PqKKP6mol3KuNvamNUrtyHYpeQseGfN_Yy47o9F8hyXkjLNLzoS60mUCJlUlzQEZTVjJimlOh7--ro_JOMZnllUzVik1Im-P4NbgMCL1r9ZgpHHX9z4kNNQ7uhlM8Gt08JGXdjGhDpzf24AUQoCBakjQDTFF2vpA0wYpdqhT8HqDW6uhy9ghAyi--G6XbGYGBP1prKP7DA4_k8yx8ZQctdBFHH_fE_J0e7Oc3Rfzxd3D7HperCeSpUKqEhQi1k3JUQIY07BGcdnAVHCGotFTpaqyklLU0HLJmDC8akpgjAMKI07I-Rc3RL3qg91CGFZ_H8z9xX_9qjeteAfhx3Rf</recordid><startdate>20150101</startdate><enddate>20150101</enddate><creator>Li, Nan</creator><creator>Xia, Wei-Yan</creator><creator>Wang, Jing</creator><creator>Liu, Zi-Li</creator><creator>Li, Qing-Yu</creator><creator>Chen, Sheng-Zhou</creator><creator>Xu, Chang-Wei</creator><creator>Lu, Xi-Hong</creator><scope/></search><sort><creationdate>20150101</creationdate><title>Manganese oxides supported on hydrogenated TiO2 nanowire array catalysts for the electrochemical oxygen evolution reaction in water electrolysis</title><author>Li, Nan ; Xia, Wei-Yan ; Wang, Jing ; Liu, Zi-Li ; Li, Qing-Yu ; Chen, Sheng-Zhou ; Xu, Chang-Wei ; Lu, Xi-Hong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-g240t-495a9eee8b51e4aaddb0b914ba7310e3bc7996564438af14003d16b5a001ae3d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Nan</creatorcontrib><creatorcontrib>Xia, Wei-Yan</creatorcontrib><creatorcontrib>Wang, Jing</creatorcontrib><creatorcontrib>Liu, Zi-Li</creatorcontrib><creatorcontrib>Li, Qing-Yu</creatorcontrib><creatorcontrib>Chen, Sheng-Zhou</creatorcontrib><creatorcontrib>Xu, Chang-Wei</creatorcontrib><creatorcontrib>Lu, Xi-Hong</creatorcontrib></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Nan</au><au>Xia, Wei-Yan</au><au>Wang, Jing</au><au>Liu, Zi-Li</au><au>Li, Qing-Yu</au><au>Chen, Sheng-Zhou</au><au>Xu, Chang-Wei</au><au>Lu, Xi-Hong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Manganese oxides supported on hydrogenated TiO2 nanowire array catalysts for the electrochemical oxygen evolution reaction in water electrolysis</atitle><date>2015-01-01</date><risdate>2015</risdate><volume>3</volume><issue>42</issue><spage>2138</spage><epage>21313</epage><pages>2138-21313</pages><issn>2050-7488</issn><eissn>2050-7496</eissn><abstract>Hydrogenated TiO 2 /MnO x nanowires (NWs) with a diameter of 50-80 nm and a length of 0.5-0.8 μm supported on carbon cloth have been successfully prepared. The entire surface of the H-TiO 2 NWs is covered uniformly by amorphous MnO x with an average thickness of 7.0 nm. The H-TiO 2 NWs are poorly active for the oxygen evolution reaction (OER) and the MnO x as a major potential feasible electrocatalyst shows a considerable activity. The onset potential shifts negatively and the current density improves not only by the enlarged surface area of the MnO x support on the H-TiO 2 NWs, but also by a synergistic effect between TiO 2 and MnO x . The presence of three manganese oxides with different valences such as MnO, Mn 2 O 3 and MnO 2 in the H-TiO 2 /MnO x NWs is apt to effect the OER due to electron transfer. The percentage of Mn 2+ increases and the percentages of Mn 3+ and Mn 4+ decrease after the test, which proves the assumption that Mn 4+ is first reduced to Mn 3+ by electron injection from H 2 O, and then Mn 3+ is further reduced to Mn 2+ when the O 2 evolution occurs during the OER in alkaline media at pH ≥ 9. Manganese oxide/hydrogenated TiO 2 core-shell nanowires exhibited enhanced electrocatalytic activity toward the oxygen evolution reaction in water electrolysis.</abstract><doi>10.1039/c5ta04964d</doi><tpages>6</tpages></addata></record>
fulltext fulltext
identifier ISSN: 2050-7488
ispartof
issn 2050-7488
2050-7496
language eng
recordid cdi_rsc_primary_c5ta04964d
source Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection
title Manganese oxides supported on hydrogenated TiO2 nanowire array catalysts for the electrochemical oxygen evolution reaction in water electrolysis
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-05T04%3A09%3A28IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-rsc&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Manganese%20oxides%20supported%20on%20hydrogenated%20TiO2%20nanowire%20array%20catalysts%20for%20the%20electrochemical%20oxygen%20evolution%20reaction%20in%20water%20electrolysis&rft.au=Li,%20Nan&rft.date=2015-01-01&rft.volume=3&rft.issue=42&rft.spage=2138&rft.epage=21313&rft.pages=2138-21313&rft.issn=2050-7488&rft.eissn=2050-7496&rft_id=info:doi/10.1039/c5ta04964d&rft_dat=%3Crsc%3Ec5ta04964d%3C/rsc%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