Role of Composition and Size of Cobalt Ferrite Nanocrystals in the Oxygen Evolution Reaction
Sub‐10 nm CoFe2O4 nanoparticles with different sizes and various compositions obtained by (partial) substitution of Co with Ni cations have been synthesized by using a one‐pot method from organic solutions by the decomposition of metal acetylacetonates in the presence of oleylamine. The electrocatal...
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creator | Chakrapani, Kalapu Bendt, Georg Hajiyani, Hamidreza Schwarzrock, Ingo Lunkenbein, Thomas Salamon, Soma Landers, Joachim Wende, Heiko Schlögl, Robert Pentcheva, Rossitza Behrens, Malte Schulz, Stephan |
description | Sub‐10 nm CoFe2O4 nanoparticles with different sizes and various compositions obtained by (partial) substitution of Co with Ni cations have been synthesized by using a one‐pot method from organic solutions by the decomposition of metal acetylacetonates in the presence of oleylamine. The electrocatalytic activity of CoFe2O4 towards the oxygen evolution reaction (OER) is clearly enhanced with a smaller size (3.1 nm) of the CoFe2O4 nanoparticles (compared with 4.5 and 5.9 nm). In addition, the catalytic activity is improved by partial substitution of Co with Ni, which also leads to a higher degree of inversion of the spinel structure. Theoretical calculations attribute the positive catalytic effect of Ni owing to the lower binding energy differences between adsorbed O and OH compared with pure cobalt or nickel ferrites, resulting in higher OER activity. Co0.5Ni0.5Fe2O4 exhibited a low overpotential of approximately 340 mV at 10 mA cm−2, a smaller Tafel slope of 51 mV dec−1, and stability over 30 h. The unique tunability of these CoFe2O4 nanocrystals provides great potential for their application as an efficient and competitive anode material in the field of electrochemical water splitting as well as for systematic fundamental studies aiming at understanding the correlation of composition and structure with performance in electrocatalysis.
Enhancing exchange: Experimental and theoretical findings show that CoxNi1−xFe2O4 nanoparticles have lower binding energy differences of O and OH as well as high intrinsic electrical conductivity with structural inversion, leading to favorable oxygen evolution reaction (OER) activity compared with pure CoFe2O4 and NiFe2O4 as well as their physical mixtures. |
doi_str_mv | 10.1002/cctc.201700376 |
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Enhancing exchange: Experimental and theoretical findings show that CoxNi1−xFe2O4 nanoparticles have lower binding energy differences of O and OH as well as high intrinsic electrical conductivity with structural inversion, leading to favorable oxygen evolution reaction (OER) activity compared with pure CoFe2O4 and NiFe2O4 as well as their physical mixtures.</description><identifier>ISSN: 1867-3880</identifier><identifier>EISSN: 1867-3899</identifier><identifier>DOI: 10.1002/cctc.201700376</identifier><language>eng</language><publisher>Weinheim: Wiley Subscription Services, Inc</publisher><subject>Binding energy ; Catalysis ; Catalytic activity ; Cobalt ferrites ; Competitive materials ; composition ; Correlation analysis ; density functional calculations ; Electrocatalysis ; Nanocrystals ; Nanoparticles ; Nickel ferrites ; oxygen evolution reaction ; Oxygen evolution reactions ; Slope stability ; Spinel ; spinel nanocrystals ; Water splitting</subject><ispartof>ChemCatChem, 2017-08, Vol.9 (15), p.2988-2995</ispartof><rights>2017 Wiley‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><rights>2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3576-1fec5351fab6559e9a85b1b7933eac5f267152f8e2edf6dba4295d32772a2cd3</citedby><cites>FETCH-LOGICAL-c3576-1fec5351fab6559e9a85b1b7933eac5f267152f8e2edf6dba4295d32772a2cd3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fcctc.201700376$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fcctc.201700376$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids></links><search><creatorcontrib>Chakrapani, Kalapu</creatorcontrib><creatorcontrib>Bendt, Georg</creatorcontrib><creatorcontrib>Hajiyani, Hamidreza</creatorcontrib><creatorcontrib>Schwarzrock, Ingo</creatorcontrib><creatorcontrib>Lunkenbein, Thomas</creatorcontrib><creatorcontrib>Salamon, Soma</creatorcontrib><creatorcontrib>Landers, Joachim</creatorcontrib><creatorcontrib>Wende, Heiko</creatorcontrib><creatorcontrib>Schlögl, Robert</creatorcontrib><creatorcontrib>Pentcheva, Rossitza</creatorcontrib><creatorcontrib>Behrens, Malte</creatorcontrib><creatorcontrib>Schulz, Stephan</creatorcontrib><title>Role of Composition and Size of Cobalt Ferrite Nanocrystals in the Oxygen Evolution Reaction</title><title>ChemCatChem</title><description>Sub‐10 nm CoFe2O4 nanoparticles with different sizes and various compositions obtained by (partial) substitution of Co with Ni cations have been synthesized by using a one‐pot method from organic solutions by the decomposition of metal acetylacetonates in the presence of oleylamine. The electrocatalytic activity of CoFe2O4 towards the oxygen evolution reaction (OER) is clearly enhanced with a smaller size (3.1 nm) of the CoFe2O4 nanoparticles (compared with 4.5 and 5.9 nm). In addition, the catalytic activity is improved by partial substitution of Co with Ni, which also leads to a higher degree of inversion of the spinel structure. Theoretical calculations attribute the positive catalytic effect of Ni owing to the lower binding energy differences between adsorbed O and OH compared with pure cobalt or nickel ferrites, resulting in higher OER activity. Co0.5Ni0.5Fe2O4 exhibited a low overpotential of approximately 340 mV at 10 mA cm−2, a smaller Tafel slope of 51 mV dec−1, and stability over 30 h. The unique tunability of these CoFe2O4 nanocrystals provides great potential for their application as an efficient and competitive anode material in the field of electrochemical water splitting as well as for systematic fundamental studies aiming at understanding the correlation of composition and structure with performance in electrocatalysis.
Enhancing exchange: Experimental and theoretical findings show that CoxNi1−xFe2O4 nanoparticles have lower binding energy differences of O and OH as well as high intrinsic electrical conductivity with structural inversion, leading to favorable oxygen evolution reaction (OER) activity compared with pure CoFe2O4 and NiFe2O4 as well as their physical mixtures.</description><subject>Binding energy</subject><subject>Catalysis</subject><subject>Catalytic activity</subject><subject>Cobalt ferrites</subject><subject>Competitive materials</subject><subject>composition</subject><subject>Correlation analysis</subject><subject>density functional calculations</subject><subject>Electrocatalysis</subject><subject>Nanocrystals</subject><subject>Nanoparticles</subject><subject>Nickel ferrites</subject><subject>oxygen evolution reaction</subject><subject>Oxygen evolution reactions</subject><subject>Slope stability</subject><subject>Spinel</subject><subject>spinel nanocrystals</subject><subject>Water splitting</subject><issn>1867-3880</issn><issn>1867-3899</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNqFkE1LAzEURYMoWKtb1wHXU_PRJJOlDK0KxULtUgiZTKIp00lNpur4653aUpeu3uVxzntwAbjGaIQRIrfGtGZEEBYIUcFPwADnXGQ0l_L0mHN0Di5SWiHEJRVsAF4WobYwOFiE9SYk3_rQQN1U8Nl_H_alrls4tTH61sIn3QQTu9TqOkHfwPbNwvlX92obOPkI9fbXX1htduESnLmes1eHOQTL6WRZPGSz-f1jcTfLDGWCZ9hZwyjDTpecMWmlzlmJSyEp7Q8xR7jAjLjcEls5XpV6TCSrKBGCaGIqOgQ3-7ObGN63NrVqFbax6T8qLInAY8KZ6KnRnjIxpBStU5vo1zp2CiO1K1DtClTHAntB7oVPX9vuH1oVxbL4c38Aa6l1OA</recordid><startdate>20170809</startdate><enddate>20170809</enddate><creator>Chakrapani, Kalapu</creator><creator>Bendt, Georg</creator><creator>Hajiyani, Hamidreza</creator><creator>Schwarzrock, Ingo</creator><creator>Lunkenbein, Thomas</creator><creator>Salamon, Soma</creator><creator>Landers, Joachim</creator><creator>Wende, Heiko</creator><creator>Schlögl, Robert</creator><creator>Pentcheva, Rossitza</creator><creator>Behrens, Malte</creator><creator>Schulz, Stephan</creator><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20170809</creationdate><title>Role of Composition and Size of Cobalt Ferrite Nanocrystals in the Oxygen Evolution Reaction</title><author>Chakrapani, Kalapu ; Bendt, Georg ; Hajiyani, Hamidreza ; Schwarzrock, Ingo ; Lunkenbein, Thomas ; Salamon, Soma ; Landers, Joachim ; Wende, Heiko ; Schlögl, Robert ; Pentcheva, Rossitza ; Behrens, Malte ; Schulz, Stephan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3576-1fec5351fab6559e9a85b1b7933eac5f267152f8e2edf6dba4295d32772a2cd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Binding energy</topic><topic>Catalysis</topic><topic>Catalytic activity</topic><topic>Cobalt ferrites</topic><topic>Competitive materials</topic><topic>composition</topic><topic>Correlation analysis</topic><topic>density functional calculations</topic><topic>Electrocatalysis</topic><topic>Nanocrystals</topic><topic>Nanoparticles</topic><topic>Nickel ferrites</topic><topic>oxygen evolution reaction</topic><topic>Oxygen evolution reactions</topic><topic>Slope stability</topic><topic>Spinel</topic><topic>spinel nanocrystals</topic><topic>Water splitting</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chakrapani, Kalapu</creatorcontrib><creatorcontrib>Bendt, Georg</creatorcontrib><creatorcontrib>Hajiyani, Hamidreza</creatorcontrib><creatorcontrib>Schwarzrock, Ingo</creatorcontrib><creatorcontrib>Lunkenbein, Thomas</creatorcontrib><creatorcontrib>Salamon, Soma</creatorcontrib><creatorcontrib>Landers, Joachim</creatorcontrib><creatorcontrib>Wende, Heiko</creatorcontrib><creatorcontrib>Schlögl, Robert</creatorcontrib><creatorcontrib>Pentcheva, Rossitza</creatorcontrib><creatorcontrib>Behrens, Malte</creatorcontrib><creatorcontrib>Schulz, Stephan</creatorcontrib><collection>CrossRef</collection><jtitle>ChemCatChem</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chakrapani, Kalapu</au><au>Bendt, Georg</au><au>Hajiyani, Hamidreza</au><au>Schwarzrock, Ingo</au><au>Lunkenbein, Thomas</au><au>Salamon, Soma</au><au>Landers, Joachim</au><au>Wende, Heiko</au><au>Schlögl, Robert</au><au>Pentcheva, Rossitza</au><au>Behrens, Malte</au><au>Schulz, Stephan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Role of Composition and Size of Cobalt Ferrite Nanocrystals in the Oxygen Evolution Reaction</atitle><jtitle>ChemCatChem</jtitle><date>2017-08-09</date><risdate>2017</risdate><volume>9</volume><issue>15</issue><spage>2988</spage><epage>2995</epage><pages>2988-2995</pages><issn>1867-3880</issn><eissn>1867-3899</eissn><abstract>Sub‐10 nm CoFe2O4 nanoparticles with different sizes and various compositions obtained by (partial) substitution of Co with Ni cations have been synthesized by using a one‐pot method from organic solutions by the decomposition of metal acetylacetonates in the presence of oleylamine. The electrocatalytic activity of CoFe2O4 towards the oxygen evolution reaction (OER) is clearly enhanced with a smaller size (3.1 nm) of the CoFe2O4 nanoparticles (compared with 4.5 and 5.9 nm). In addition, the catalytic activity is improved by partial substitution of Co with Ni, which also leads to a higher degree of inversion of the spinel structure. Theoretical calculations attribute the positive catalytic effect of Ni owing to the lower binding energy differences between adsorbed O and OH compared with pure cobalt or nickel ferrites, resulting in higher OER activity. Co0.5Ni0.5Fe2O4 exhibited a low overpotential of approximately 340 mV at 10 mA cm−2, a smaller Tafel slope of 51 mV dec−1, and stability over 30 h. The unique tunability of these CoFe2O4 nanocrystals provides great potential for their application as an efficient and competitive anode material in the field of electrochemical water splitting as well as for systematic fundamental studies aiming at understanding the correlation of composition and structure with performance in electrocatalysis.
Enhancing exchange: Experimental and theoretical findings show that CoxNi1−xFe2O4 nanoparticles have lower binding energy differences of O and OH as well as high intrinsic electrical conductivity with structural inversion, leading to favorable oxygen evolution reaction (OER) activity compared with pure CoFe2O4 and NiFe2O4 as well as their physical mixtures.</abstract><cop>Weinheim</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/cctc.201700376</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Binding energy Catalysis Catalytic activity Cobalt ferrites Competitive materials composition Correlation analysis density functional calculations Electrocatalysis Nanocrystals Nanoparticles Nickel ferrites oxygen evolution reaction Oxygen evolution reactions Slope stability Spinel spinel nanocrystals Water splitting |
title | Role of Composition and Size of Cobalt Ferrite Nanocrystals in the Oxygen Evolution Reaction |
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