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Enhancing the oxygen evolution reaction of cobalt hydroxide by fabricating nanocomposites with fluorine-doped graphene oxide
Fluorine and nitrogen codoped cobalt hydroxide-graphene oxide nanocomposites (N,F-Co(OH) 2 /GO) were synthesized by a simple hydrothermal method and demonstrated highly enhanced oxygen evolution activity in an alkaline medium. N,F-Co(OH) 2 /GO synthesized under optimized reaction conditions required...
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Published in: | Dalton transactions : an international journal of inorganic chemistry 2023-03, Vol.52 (12), p.3877-3883 |
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creator | Muthukumar, Pandi Nantheeswaran, Periyappan Mariappan, Mariappan Pannipara, Mehboobali Al-Sehemi, Abdullah G Anthony, Savarimuthu Philip |
description | Fluorine and nitrogen codoped cobalt hydroxide-graphene oxide nanocomposites (N,F-Co(OH)
2
/GO) were synthesized by a simple hydrothermal method and demonstrated highly enhanced oxygen evolution activity in an alkaline medium. N,F-Co(OH)
2
/GO synthesized under optimized reaction conditions required an overpotential of 228 mV to produce the benchmark current density of 10 mA cm
−2
(scan rate 1 mV s
−1
). In contrast, N,F-Co(OH)
2
without GO and Co(OH)
2
/GO without fluorine required higher overpotentials (370 (N,F-Co(OH)
2
) and 325 mV (Co(OH)
2
/GO)) for producing the current density of 10 mA cm
−2
. The low Tafel slope (52.6 mV dec
−1
) and charge transfer resistance, and high electrochemical double layer capacitance of N,F-Co(OH)
2
/GO compared to N,F-Co(OH)
2
indicate faster kinetics at the electrode-catalyst interface. The N,F-Co(OH)
2
/GO catalyst showed good stability over 30 h. High-resolution transmission electron microscope (HR-TEM) images showed good dispersion of polycrystalline Co(OH)
2
nanoparticles in the GO matrix. X-ray photoelectron spectroscopic (XPS) analysis revealed the coexistence of Co
2+
/Co
3+
and the doping of nitrogen and fluorine in N,F-Co(OH)
2
/GO. XPS further revealed the presence of F in its ionic state and being covalently attached to GO. The integration of highly electronegative F with GO stabilizes the Co
2+
active centre along with improving the charge transfer and adsorption process that contributes to improved OER. Thus, the present work reports a facile method for preparing F-doped GO-Co(OH)
2
electrocatalysts with enhanced OER activity under alkaline conditions.
The integration of electronegative F into graphene oxide improves the charge-transfer kinetics and stability of the Co
2+
active center and showed enhanced OER activity. |
doi_str_mv | 10.1039/d2dt04169c |
format | article |
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2
/GO) were synthesized by a simple hydrothermal method and demonstrated highly enhanced oxygen evolution activity in an alkaline medium. N,F-Co(OH)
2
/GO synthesized under optimized reaction conditions required an overpotential of 228 mV to produce the benchmark current density of 10 mA cm
−2
(scan rate 1 mV s
−1
). In contrast, N,F-Co(OH)
2
without GO and Co(OH)
2
/GO without fluorine required higher overpotentials (370 (N,F-Co(OH)
2
) and 325 mV (Co(OH)
2
/GO)) for producing the current density of 10 mA cm
−2
. The low Tafel slope (52.6 mV dec
−1
) and charge transfer resistance, and high electrochemical double layer capacitance of N,F-Co(OH)
2
/GO compared to N,F-Co(OH)
2
indicate faster kinetics at the electrode-catalyst interface. The N,F-Co(OH)
2
/GO catalyst showed good stability over 30 h. High-resolution transmission electron microscope (HR-TEM) images showed good dispersion of polycrystalline Co(OH)
2
nanoparticles in the GO matrix. X-ray photoelectron spectroscopic (XPS) analysis revealed the coexistence of Co
2+
/Co
3+
and the doping of nitrogen and fluorine in N,F-Co(OH)
2
/GO. XPS further revealed the presence of F in its ionic state and being covalently attached to GO. The integration of highly electronegative F with GO stabilizes the Co
2+
active centre along with improving the charge transfer and adsorption process that contributes to improved OER. Thus, the present work reports a facile method for preparing F-doped GO-Co(OH)
2
electrocatalysts with enhanced OER activity under alkaline conditions.
The integration of electronegative F into graphene oxide improves the charge-transfer kinetics and stability of the Co
2+
active center and showed enhanced OER activity.</description><identifier>ISSN: 1477-9226</identifier><identifier>EISSN: 1477-9234</identifier><identifier>DOI: 10.1039/d2dt04169c</identifier><identifier>PMID: 36876484</identifier><language>eng</language><publisher>England: Royal Society of Chemistry</publisher><subject>Catalysts ; Charge transfer ; Chemical synthesis ; Cobalt ; Current density ; Electrocatalysts ; Electronegativity ; Fluorine ; Graphene ; Interface stability ; Nanocomposites ; Nanoparticles ; Nitrogen ; Oxygen evolution reactions ; Photoelectrons ; Reaction kinetics ; X ray photoelectron spectroscopy</subject><ispartof>Dalton transactions : an international journal of inorganic chemistry, 2023-03, Vol.52 (12), p.3877-3883</ispartof><rights>Copyright Royal Society of Chemistry 2023</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c337t-48a3db463a1c7708917f09cb93f5a2c55b567441fb2157cb10fb7dd45d6085523</citedby><cites>FETCH-LOGICAL-c337t-48a3db463a1c7708917f09cb93f5a2c55b567441fb2157cb10fb7dd45d6085523</cites><orcidid>0000-0002-9023-0920 ; 0000-0003-4714-2666</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36876484$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Muthukumar, Pandi</creatorcontrib><creatorcontrib>Nantheeswaran, Periyappan</creatorcontrib><creatorcontrib>Mariappan, Mariappan</creatorcontrib><creatorcontrib>Pannipara, Mehboobali</creatorcontrib><creatorcontrib>Al-Sehemi, Abdullah G</creatorcontrib><creatorcontrib>Anthony, Savarimuthu Philip</creatorcontrib><title>Enhancing the oxygen evolution reaction of cobalt hydroxide by fabricating nanocomposites with fluorine-doped graphene oxide</title><title>Dalton transactions : an international journal of inorganic chemistry</title><addtitle>Dalton Trans</addtitle><description>Fluorine and nitrogen codoped cobalt hydroxide-graphene oxide nanocomposites (N,F-Co(OH)
2
/GO) were synthesized by a simple hydrothermal method and demonstrated highly enhanced oxygen evolution activity in an alkaline medium. N,F-Co(OH)
2
/GO synthesized under optimized reaction conditions required an overpotential of 228 mV to produce the benchmark current density of 10 mA cm
−2
(scan rate 1 mV s
−1
). In contrast, N,F-Co(OH)
2
without GO and Co(OH)
2
/GO without fluorine required higher overpotentials (370 (N,F-Co(OH)
2
) and 325 mV (Co(OH)
2
/GO)) for producing the current density of 10 mA cm
−2
. The low Tafel slope (52.6 mV dec
−1
) and charge transfer resistance, and high electrochemical double layer capacitance of N,F-Co(OH)
2
/GO compared to N,F-Co(OH)
2
indicate faster kinetics at the electrode-catalyst interface. The N,F-Co(OH)
2
/GO catalyst showed good stability over 30 h. High-resolution transmission electron microscope (HR-TEM) images showed good dispersion of polycrystalline Co(OH)
2
nanoparticles in the GO matrix. X-ray photoelectron spectroscopic (XPS) analysis revealed the coexistence of Co
2+
/Co
3+
and the doping of nitrogen and fluorine in N,F-Co(OH)
2
/GO. XPS further revealed the presence of F in its ionic state and being covalently attached to GO. The integration of highly electronegative F with GO stabilizes the Co
2+
active centre along with improving the charge transfer and adsorption process that contributes to improved OER. Thus, the present work reports a facile method for preparing F-doped GO-Co(OH)
2
electrocatalysts with enhanced OER activity under alkaline conditions.
The integration of electronegative F into graphene oxide improves the charge-transfer kinetics and stability of the Co
2+
active center and showed enhanced OER activity.</description><subject>Catalysts</subject><subject>Charge transfer</subject><subject>Chemical synthesis</subject><subject>Cobalt</subject><subject>Current density</subject><subject>Electrocatalysts</subject><subject>Electronegativity</subject><subject>Fluorine</subject><subject>Graphene</subject><subject>Interface stability</subject><subject>Nanocomposites</subject><subject>Nanoparticles</subject><subject>Nitrogen</subject><subject>Oxygen evolution reactions</subject><subject>Photoelectrons</subject><subject>Reaction kinetics</subject><subject>X ray photoelectron spectroscopy</subject><issn>1477-9226</issn><issn>1477-9234</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNpdkctr3DAQh0VpaZJtL723CHIJBSd6WvaxbB4tBHJJzkbPtYJXciW5yUL--Hiz6QYylxmYj28GfgB8w-gUI9qeGWIKYrhu9QdwiJkQVUso-7ifSX0AjnK-R4gQxMlncEDrRtSsYYfg6SL0MmgfVrD0FsbHzcoGaP_FYSo-Bpis1C9DdFBHJYcC-41J8dEbC9UGOqmS17JsBUGGqON6jNkXm-GDLz10wxSTD7YycbQGrpIcexu2h2bBF_DJySHbr699Ae4uL26Xv6vrm6s_y1_XlaZUlIo1khrFaiqxFgI1LRYOtVq11HFJNOeK14Ix7BTBXGiFkVPCGMZNjRrOCV2Ak513TPHvZHPp1j5rOwwy2DjljoiGikbgGs3o8Tv0Pk4pzN9tqUaQls61AD93lE4x52RdNya_lmnTYdRtM-nOyfntSybLGf7xqpzU2po9-j-EGfi-A1LW--1bqPQZuGiSYg</recordid><startdate>20230321</startdate><enddate>20230321</enddate><creator>Muthukumar, Pandi</creator><creator>Nantheeswaran, Periyappan</creator><creator>Mariappan, Mariappan</creator><creator>Pannipara, Mehboobali</creator><creator>Al-Sehemi, Abdullah G</creator><creator>Anthony, Savarimuthu Philip</creator><general>Royal Society of Chemistry</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-9023-0920</orcidid><orcidid>https://orcid.org/0000-0003-4714-2666</orcidid></search><sort><creationdate>20230321</creationdate><title>Enhancing the oxygen evolution reaction of cobalt hydroxide by fabricating nanocomposites with fluorine-doped graphene oxide</title><author>Muthukumar, Pandi ; Nantheeswaran, Periyappan ; Mariappan, Mariappan ; Pannipara, Mehboobali ; Al-Sehemi, Abdullah G ; Anthony, Savarimuthu Philip</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c337t-48a3db463a1c7708917f09cb93f5a2c55b567441fb2157cb10fb7dd45d6085523</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Catalysts</topic><topic>Charge transfer</topic><topic>Chemical synthesis</topic><topic>Cobalt</topic><topic>Current density</topic><topic>Electrocatalysts</topic><topic>Electronegativity</topic><topic>Fluorine</topic><topic>Graphene</topic><topic>Interface stability</topic><topic>Nanocomposites</topic><topic>Nanoparticles</topic><topic>Nitrogen</topic><topic>Oxygen evolution reactions</topic><topic>Photoelectrons</topic><topic>Reaction kinetics</topic><topic>X ray photoelectron spectroscopy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Muthukumar, Pandi</creatorcontrib><creatorcontrib>Nantheeswaran, Periyappan</creatorcontrib><creatorcontrib>Mariappan, Mariappan</creatorcontrib><creatorcontrib>Pannipara, Mehboobali</creatorcontrib><creatorcontrib>Al-Sehemi, Abdullah G</creatorcontrib><creatorcontrib>Anthony, Savarimuthu Philip</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>MEDLINE - Academic</collection><jtitle>Dalton transactions : an international journal of inorganic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Muthukumar, Pandi</au><au>Nantheeswaran, Periyappan</au><au>Mariappan, Mariappan</au><au>Pannipara, Mehboobali</au><au>Al-Sehemi, Abdullah G</au><au>Anthony, Savarimuthu Philip</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Enhancing the oxygen evolution reaction of cobalt hydroxide by fabricating nanocomposites with fluorine-doped graphene oxide</atitle><jtitle>Dalton transactions : an international journal of inorganic chemistry</jtitle><addtitle>Dalton Trans</addtitle><date>2023-03-21</date><risdate>2023</risdate><volume>52</volume><issue>12</issue><spage>3877</spage><epage>3883</epage><pages>3877-3883</pages><issn>1477-9226</issn><eissn>1477-9234</eissn><abstract>Fluorine and nitrogen codoped cobalt hydroxide-graphene oxide nanocomposites (N,F-Co(OH)
2
/GO) were synthesized by a simple hydrothermal method and demonstrated highly enhanced oxygen evolution activity in an alkaline medium. N,F-Co(OH)
2
/GO synthesized under optimized reaction conditions required an overpotential of 228 mV to produce the benchmark current density of 10 mA cm
−2
(scan rate 1 mV s
−1
). In contrast, N,F-Co(OH)
2
without GO and Co(OH)
2
/GO without fluorine required higher overpotentials (370 (N,F-Co(OH)
2
) and 325 mV (Co(OH)
2
/GO)) for producing the current density of 10 mA cm
−2
. The low Tafel slope (52.6 mV dec
−1
) and charge transfer resistance, and high electrochemical double layer capacitance of N,F-Co(OH)
2
/GO compared to N,F-Co(OH)
2
indicate faster kinetics at the electrode-catalyst interface. The N,F-Co(OH)
2
/GO catalyst showed good stability over 30 h. High-resolution transmission electron microscope (HR-TEM) images showed good dispersion of polycrystalline Co(OH)
2
nanoparticles in the GO matrix. X-ray photoelectron spectroscopic (XPS) analysis revealed the coexistence of Co
2+
/Co
3+
and the doping of nitrogen and fluorine in N,F-Co(OH)
2
/GO. XPS further revealed the presence of F in its ionic state and being covalently attached to GO. The integration of highly electronegative F with GO stabilizes the Co
2+
active centre along with improving the charge transfer and adsorption process that contributes to improved OER. Thus, the present work reports a facile method for preparing F-doped GO-Co(OH)
2
electrocatalysts with enhanced OER activity under alkaline conditions.
The integration of electronegative F into graphene oxide improves the charge-transfer kinetics and stability of the Co
2+
active center and showed enhanced OER activity.</abstract><cop>England</cop><pub>Royal Society of Chemistry</pub><pmid>36876484</pmid><doi>10.1039/d2dt04169c</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-9023-0920</orcidid><orcidid>https://orcid.org/0000-0003-4714-2666</orcidid></addata></record> |
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language | eng |
recordid | cdi_pubmed_primary_36876484 |
source | Royal Society of Chemistry |
subjects | Catalysts Charge transfer Chemical synthesis Cobalt Current density Electrocatalysts Electronegativity Fluorine Graphene Interface stability Nanocomposites Nanoparticles Nitrogen Oxygen evolution reactions Photoelectrons Reaction kinetics X ray photoelectron spectroscopy |
title | Enhancing the oxygen evolution reaction of cobalt hydroxide by fabricating nanocomposites with fluorine-doped graphene oxide |
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