Synthesis of nano-TaOx oxygen reduction reaction catalysts on multi-walled carbon nanotubes connected via a decomposition of oxy-tantalum phthalocyanineElectronic supplementary information (ESI) available: RRDE voltammograms. See DOI: 10.1039/c5cp00317b
Nano-TaO x particles were supported on multi-walled carbon nanotubes via the thermal decomposition of oxy-tantalum phthalocyanine. The phthalocyanine-derived carbon connected TaO x particles with the nanotube-support to provide a conductive path. The oxygen reduction reaction activity, which solely...
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creator | Ishihara, A Chisaka, M Ohgi, Y Matsuzawa, K Mitsushima, S Ota, K |
description | Nano-TaO
x
particles were supported on multi-walled carbon nanotubes
via
the thermal decomposition of oxy-tantalum phthalocyanine. The phthalocyanine-derived carbon connected TaO
x
particles with the nanotube-support to provide a conductive path. The oxygen reduction reaction activity, which solely originated from TaO
x
, was above 0.9 V with larger currents than conventional TaO
x
particles in acidic media.
Nano-TaO
x
particles were supported on MWCNTs
via
a thermal decomposition of oxy-tantalum phthalocyanine. The ORR activity solely-originated from nano-TaO
x
was above 0.9 V
versus
RHE with larger currents than conventional micro-TaO
x
in acidic media. |
doi_str_mv | 10.1039/c5cp00317b |
format | Article |
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x
particles were supported on multi-walled carbon nanotubes
via
the thermal decomposition of oxy-tantalum phthalocyanine. The phthalocyanine-derived carbon connected TaO
x
particles with the nanotube-support to provide a conductive path. The oxygen reduction reaction activity, which solely originated from TaO
x
, was above 0.9 V with larger currents than conventional TaO
x
particles in acidic media.
Nano-TaO
x
particles were supported on MWCNTs
via
a thermal decomposition of oxy-tantalum phthalocyanine. The ORR activity solely-originated from nano-TaO
x
was above 0.9 V
versus
RHE with larger currents than conventional micro-TaO
x
in acidic media.</description><identifier>ISSN: 1463-9076</identifier><identifier>EISSN: 1463-9084</identifier><identifier>DOI: 10.1039/c5cp00317b</identifier><language>eng</language><creationdate>2015-03</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>314,780,784,27922,27923</link.rule.ids></links><search><creatorcontrib>Ishihara, A</creatorcontrib><creatorcontrib>Chisaka, M</creatorcontrib><creatorcontrib>Ohgi, Y</creatorcontrib><creatorcontrib>Matsuzawa, K</creatorcontrib><creatorcontrib>Mitsushima, S</creatorcontrib><creatorcontrib>Ota, K</creatorcontrib><title>Synthesis of nano-TaOx oxygen reduction reaction catalysts on multi-walled carbon nanotubes connected via a decomposition of oxy-tantalum phthalocyanineElectronic supplementary information (ESI) available: RRDE voltammograms. See DOI: 10.1039/c5cp00317b</title><description>Nano-TaO
x
particles were supported on multi-walled carbon nanotubes
via
the thermal decomposition of oxy-tantalum phthalocyanine. The phthalocyanine-derived carbon connected TaO
x
particles with the nanotube-support to provide a conductive path. The oxygen reduction reaction activity, which solely originated from TaO
x
, was above 0.9 V with larger currents than conventional TaO
x
particles in acidic media.
Nano-TaO
x
particles were supported on MWCNTs
via
a thermal decomposition of oxy-tantalum phthalocyanine. The ORR activity solely-originated from nano-TaO
x
was above 0.9 V
versus
RHE with larger currents than conventional micro-TaO
x
in acidic media.</description><issn>1463-9076</issn><issn>1463-9084</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNqFkM1Lw0AQxYMoWD8u3oXxpofUDemH7dVG7KnQ9l4mm0m7sl_sbmrzxwvdVtGDoKd5zHvzezBJcpOxbsby0SPvc8tYng3Lk6ST9QZ5OmJPvdNvPRycJxfevzHGsn6Wd5KPRavDhrzwYGrQqE26xNkOzK5dkwZHVcODMAeFn4JjQNn6EA80qEYGkb6jlFRFx5Vxd4CEpiQP3GhNPERrKxAQKuJGWePFERT7YksaUEdgo8Buwgal4S1qoamQ8dIZLTj4xlpJimLOtSB0bZzCI-K-WEwfALcoJJaSxjCfTwrYGhlQKbN2qHwXFkQwmU3H8PtJV8lZjdLT9de8TG5fiuXza-o8X1knVCxc_cTz__27v_yVrep8D0zWius</recordid><startdate>20150311</startdate><enddate>20150311</enddate><creator>Ishihara, A</creator><creator>Chisaka, M</creator><creator>Ohgi, Y</creator><creator>Matsuzawa, K</creator><creator>Mitsushima, S</creator><creator>Ota, K</creator><scope/></search><sort><creationdate>20150311</creationdate><title>Synthesis of nano-TaOx oxygen reduction reaction catalysts on multi-walled carbon nanotubes connected via a decomposition of oxy-tantalum phthalocyanineElectronic supplementary information (ESI) available: RRDE voltammograms. See DOI: 10.1039/c5cp00317b</title><author>Ishihara, A ; Chisaka, M ; Ohgi, Y ; Matsuzawa, K ; Mitsushima, S ; Ota, K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-rsc_primary_c5cp00317b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ishihara, A</creatorcontrib><creatorcontrib>Chisaka, M</creatorcontrib><creatorcontrib>Ohgi, Y</creatorcontrib><creatorcontrib>Matsuzawa, K</creatorcontrib><creatorcontrib>Mitsushima, S</creatorcontrib><creatorcontrib>Ota, K</creatorcontrib></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ishihara, A</au><au>Chisaka, M</au><au>Ohgi, Y</au><au>Matsuzawa, K</au><au>Mitsushima, S</au><au>Ota, K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis of nano-TaOx oxygen reduction reaction catalysts on multi-walled carbon nanotubes connected via a decomposition of oxy-tantalum phthalocyanineElectronic supplementary information (ESI) available: RRDE voltammograms. See DOI: 10.1039/c5cp00317b</atitle><date>2015-03-11</date><risdate>2015</risdate><volume>17</volume><issue>12</issue><spage>7643</spage><epage>7647</epage><pages>7643-7647</pages><issn>1463-9076</issn><eissn>1463-9084</eissn><abstract>Nano-TaO
x
particles were supported on multi-walled carbon nanotubes
via
the thermal decomposition of oxy-tantalum phthalocyanine. The phthalocyanine-derived carbon connected TaO
x
particles with the nanotube-support to provide a conductive path. The oxygen reduction reaction activity, which solely originated from TaO
x
, was above 0.9 V with larger currents than conventional TaO
x
particles in acidic media.
Nano-TaO
x
particles were supported on MWCNTs
via
a thermal decomposition of oxy-tantalum phthalocyanine. The ORR activity solely-originated from nano-TaO
x
was above 0.9 V
versus
RHE with larger currents than conventional micro-TaO
x
in acidic media.</abstract><doi>10.1039/c5cp00317b</doi><tpages>5</tpages></addata></record> |
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source | Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
title | Synthesis of nano-TaOx oxygen reduction reaction catalysts on multi-walled carbon nanotubes connected via a decomposition of oxy-tantalum phthalocyanineElectronic supplementary information (ESI) available: RRDE voltammograms. See DOI: 10.1039/c5cp00317b |
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